mgi_id	symbol	alleles	background	mp_id	mp_term	new_mp_id
MGI:1929608	Aatf	Aatf<Gt(pGT1.8geo)3Pgr>/Aatf<Gt(pGT1.8geo)3Pgr>	either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * NMRI)	MP:0004957	abnormal blastocyst morphology	CCO:MP0004957
MGI:1929608	Aatf	Aatf<Gt(pGT1.8geo)3Pgr>/Aatf<Gt(pGT1.8geo)3Pgr>	either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * NMRI)	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:1929608	Aatf	Aatf<Gt(pGT1.8geo)3Pgr>/Aatf<Gt(pGT1.8geo)3Pgr>	either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * NMRI)	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1929608	Aatf	Aatf<Gt(pGT1.8geo)3Pgr>/Aatf<Gt(pGT1.8geo)3Pgr>	either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * NMRI)	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1929608	Aatf	Aatf<Gt(pGT1.8geo)3Pgr>/Aatf<Gt(pGT1.8geo)3Pgr>	either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * NMRI)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1929608	Aatf	Aatf<Gt(pGT1.8geo)3Pgr>/Aatf<Gt(pGT1.8geo)3Pgr>	either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * NMRI)	MP:0002663	failure to form blastocele	CCO:MP0002663
MGI:1929608	Aatf	Aatf<Gt(pGT1.8geo)3Pgr>/Aatf<Gt(pGT1.8geo)3Pgr>	either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * NMRI)	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0000467	abnormal esophagus morphology	CCO:MP0000467
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0001861	lung inflammation	CCO:MP0001861
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0000493	rectal prolapse	CCO:MP0000493
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0005150	cachexia	CCO:MP0005150
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0003643	spleen atrophy	CCO:MP0003643
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0003644	thymus atrophy	CCO:MP0003644
MGI:87859	Abl1	Abl1<tm1Mlg>/Abl1<tm1Mlg>	involves: 129S/SvEv * C57BL/6J	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<+>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<+>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0009216	abnormal peritoneum morphology	CCO:MP0009216
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<+>,Abl2<tm1Ajk>/Abl2<tm1Ajk>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<tm1Ajk>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0002621	delayed neural tube closure	CCO:MP0002621
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<tm1Ajk>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<tm1Ajk>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<+>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0001785	edema	CCO:MP0001785
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<tm1Ajk>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<+>,Abl2<tm1Ajk>/Abl2<tm1Ajk>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<tm1Ajk>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0004261	abnormal embryonic neuroepithelium morphology	CCO:MP0004261
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<+>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0000292	distended pericardial sacs	CCO:MP0000292
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<+>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0005435	hemoperitoneum	CCO:MP0005435
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<+>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0001787	pericardial edema	CCO:MP0001787
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<+>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0005244	hemopericardium	CCO:MP0005244
MGI:87859	Abl1	"Abl1<tm1Mlg>/Abl1<tm1Mlg>,Abl2<tm1Ajk>/Abl2<tm1Ajk>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6J	MP:0005244	hemopericardium	CCO:MP0005244
MGI:87859	Abl1	"Abl1<tm1Ajk>/Abl1<tm1Ajk>,Abl2<tm1Ajk>/Abl2<tm1Ajk>,Tg(Nes-cre)1Kag/?"	involves: 129S4/SvJae	MP:0005442	abnormal pyramidal neuron morphology	CCO:MP0005442
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	involves: 129P2/OlaHsd * C57BL/6 * ICR	MP:0001377	abnormal copulation frequency	CCO:MP0001377
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	involves: 129P2/OlaHsd * C57BL/6 * ICR	MP:0001935	decreased litter size	CCO:MP0001935
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	MP:0001729	impaired embryo implantation	CCO:MP0001729
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	MP:0008489	postnatal slow weight gain	CCO:MP0008489
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	MP:0002566	abnormal sexual interaction	CCO:MP0002566
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	involves: 129P2/OlaHsd * C57BL/6 * ICR	MP:0009326	abnormal maternal crouching	CCO:MP0009326
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	MP:0005121	decreased circulating prolactin level	CCO:MP0005121
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	B6.129-Adcyap1<tm1Nms>	MP:0005185	decreased circulating progesterone level	CCO:MP0005185
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	involves: 129P2/OlaHsd * C57BL/6 * ICR	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:105094	Adcyap1	Adcyap1<tm1Eid>/Adcyap1<tm1Eid>	involves: 129S4/SvJae * C57BL/6	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0000759	abnormal skeletal muscle morphology	CCO:MP0000759
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0001263	weight loss	CCO:MP0001263
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0001783	decreased white adipose tissue amount	CCO:MP0001783
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0001777	abnormal body temperature regulation	CCO:MP0001777
MGI:105094	Adcyap1	Adcyap1<tm1Eid>/Adcyap1<tm1Eid>	involves: 129S4/SvJae * C57BL/6	MP:0003962	abnormal adrenaline level	CCO:MP0003962
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	MP:0001921	reduced fertility	CCO:MP0001921
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0005439	decreased glycogen level	CCO:MP0005439
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0005178	increased circulating cholesterol level	CCO:MP0005178
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0001552	increased circulating triglyceride level	CCO:MP0001552
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0002575	increased circulating ketone body level	CCO:MP0002575
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	MP:0001364	decreased anxiety-related response	CCO:MP0001364
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0001745	increased circulating corticosterone level	CCO:MP0001745
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0001554	increased circulating free fatty acid level	CCO:MP0001554
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	MP:0001442	decreased grooming behavior	CCO:MP0001442
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	MP:0001399	hyperactivity	CCO:MP0001399
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	MP:0001415	increased exploration in new environment	CCO:MP0001415
MGI:105094	Adcyap1	Adcyap1<tm1Aba>/Adcyap1<tm1Aba>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * ICR)	MP:0002574	increased vertical activity	CCO:MP0002574
MGI:105094	Adcyap1	Adcyap1<tm1Nms>/Adcyap1<tm1Nms>	either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6)	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:105094	Adcyap1	Adcyap1<tm1Clw>/Adcyap1<tm1Clw>	involves: 129S4/SvJae * C57BL/6	MP:0002561	abnormal circadian phase	CCO:MP0002561
MGI:105094	Adcyap1	Adcyap1<tm1Clw>/Adcyap1<tm1Clw>	involves: 129S4/SvJae * C57BL/6	MP:0001399	hyperactivity	CCO:MP0001399
MGI:105094	Adcyap1	Adcyap1<tm1Clw>/Adcyap1<tm1Clw>	involves: 129S4/SvJae * C57BL/6	MP:0002563	shortened circadian period	CCO:MP0002563
MGI:105094	Adcyap1	Adcyap1<tm1Clw>/Adcyap1<tm1Clw>	involves: 129S4/SvJae * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<b-2>/Ahr<b-2>	A/He	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:105043	Ahr	Ahr<tm4.1Bra>/Ahr<tm4.1Bra>	involves: 129/Sv * C57BL/6	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<tm4.1Bra>/Ahr<tm4.1Bra>	involves: 129/Sv * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:105043	Ahr	Ahr<tm4.1Bra>/Ahr<tm4.1Bra>	involves: 129/Sv * C57BL/6	MP:0000274	enlarged heart	CCO:MP0000274
MGI:105043	Ahr	Ahr<tm4.1Bra>/Ahr<tm4.1Bra>	involves: 129/Sv * C57BL/6	MP:0000601	small liver	CCO:MP0000601
MGI:105043	Ahr	Ahr<d>/Ahr<d>	AKR	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6J	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6J	MP:0001935	decreased litter size	CCO:MP0001935
MGI:105043	Ahr	Ahr<b-1>/Ahr<b-1>	C57BL/6	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:105043	Ahr	Ahr<d>/Ahr<d>	involves: 129S1/SvImJ * C57BL/6J	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:105043	Ahr	Ahr<d>/Ahr<d>	B6.D2-Ahr<d>	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<tm1(AHR)Mym>/Ahr<tm1(AHR)Mym>	B6.129P2-Ahr<tm1(AHR)Mym>	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<d>/Ahr<d>	involves: 129S1/SvImJ * C57BL/6J	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:105043	Ahr	Ahr<tm4.1Bra>/Ahr<tm4.1Bra>	involves: 129/Sv * C57BL/6	MP:0004004	patent ductus venosus	CCO:MP0004004
MGI:105043	Ahr	Ahr<b-2>/Ahr<b-2>	C3H/He	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:105043	Ahr	Ahr<b-1>/Ahr<b-1>	C58	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:105043	Ahr	Ahr<tm4.1Bra>/Ahr<tm4.1Bra>	involves: 129/Sv * C57BL/6	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:105043	Ahr	Ahr<d>/Ahr<d>	DBA/2J	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<b-1>/Ahr<d>	involves: 129S1/SvImJ * C57BL/6J	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:105043	Ahr	Ahr<b-1>/Ahr<d>	involves: 129S1/SvImJ * C57BL/6J	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:105043	Ahr	Ahr<d>/Ahr<d>	DBA/2	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<b-1>/Ahr<d>	involves: C57BL/6 * DBA/2	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001192	scaly skin	CCO:MP0001192
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001853	heart inflammation	CCO:MP0001853
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000414	alopecia	CCO:MP0000414
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001120	abnormal uterus morphology	CCO:MP0001120
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0002816	colitis	CCO:MP0002816
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001212	skin lesions	CCO:MP0001212
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001200	thick skin	CCO:MP0001200
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001209	spontaneous skin ulceration	CCO:MP0001209
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000692	small spleen	CCO:MP0000692
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001935	decreased litter size	CCO:MP0001935
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0002028	hepatoma	CCO:MP0002028
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000274	enlarged heart	CCO:MP0000274
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000495	abnormal colon morphology	CCO:MP0000495
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001665	chronic diarrhea	CCO:MP0001665
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0003141	cardiac fibrosis	CCO:MP0003141
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0009600	hypergranulosis	CCO:MP0009600
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0008479	decreased spleen white pulp amount	CCO:MP0008479
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0004111	abnormal coronary artery morphology	CCO:MP0004111
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0003809	abnormal hair shaft morphology	CCO:MP0003809
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0003402	decreased liver weight	CCO:MP0003402
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0003333	liver fibrosis	CCO:MP0003333
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0003324	liver adenoma	CCO:MP0003324
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000493	rectal prolapse	CCO:MP0000493
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0003254	bile duct inflammation	CCO:MP0003254
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0002356	abnormal spleen red pulp morphology	CCO:MP0002356
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0002975	vascular smooth muscle hypertrophy	CCO:MP0002975
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0002833	increased heart weight	CCO:MP0002833
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000609	abnormal liver physiology	CCO:MP0000609
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0005048	thrombosis	CCO:MP0005048
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000405	abnormal auchene hairs	CCO:MP0000405
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001874	acanthosis	CCO:MP0001874
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001855	atrial thrombosis	CCO:MP0001855
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000694	spleen hypoplasia	CCO:MP0000694
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0003299	gastric polyps	CCO:MP0003299
MGI:105043	Ahr	Ahr<tm2Bra>/Ahr<tm2Bra>	involves: 129/Sv * C57BL/6	MP:0003402	decreased liver weight	CCO:MP0003402
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008484	decreased spleen germinal center size	CCO:MP0008484
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	MP:0002209	decreased germ cell number	CCO:MP0002209
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	MP:0001928	abnormal ovulation	CCO:MP0001928
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	MP:0001127	small ovary	CCO:MP0001127
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	MP:0002680	decreased corpora lutea number	CCO:MP0002680
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ	MP:0004004	patent ductus venosus	CCO:MP0004004
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000603	pale liver	CCO:MP0000603
MGI:105043	Ahr	"Ahr<tm1Yfk>/Ahr<tm1Yfk>,Nfe2l2<tm1Mym>/Nfe2l2<tm1Mym>"	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J * ICR	MP:0008875	abnormal pharmacokinetics of xenobiotics	CCO:MP0008875
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004004	patent ductus venosus	CCO:MP0004004
MGI:105043	Ahr	"Ahr<tm1Yfk>/Ahr<tm1Yfk>,Nfe2l2<tm1Mym>/Nfe2l2<tm1Mym>"	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J * ICR	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:105043	Ahr	Ahr<tm2Bra>/Ahr<tm2Bra>	involves: 129/Sv * C57BL/6	MP:0002833	increased heart weight	CCO:MP0002833
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:105043	Ahr	Ahr<tm2Bra>/Ahr<tm2Bra>	involves: 129/Sv * C57BL/6	MP:0004952	increased spleen weight	CCO:MP0004952
MGI:105043	Ahr	Ahr<tm2Bra>/Ahr<tm2Bra>	involves: 129/Sv * C57BL/6	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	"Ahr<tm1Yfk>/Ahr<tm1Yfk>,Nfe2l2<tm1Mym>/Nfe2l2<tm1Mym>"	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J * ICR	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:105043	Ahr	Ahr<tm1Yfk>/Ahr<tm1Yfk>	involves: 129S/SvEv * C57BL/6J	MP:0008875	abnormal pharmacokinetics of xenobiotics	CCO:MP0008875
MGI:105043	Ahr	Ahr<tm1Yfk>/Ahr<tm1Yfk>	involves: 129S/SvEv * C57BL/6J	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<tm1Yfk>/Ahr<tm1Yfk>	involves: 129S/SvEv * C57BL/6J	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:105043	Ahr	Ahr<b-1>/Ahr<b-1>	involves: C57BL/6J * DBA/2J	MP:0001790	abnormal immune system physiology	CCO:MP0001790
MGI:105043	Ahr	Ahr<b-1>/Ahr<b-1>	C57BL/6J	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:105043	Ahr	Ahr<b-1>/Ahr<b-1>	C57BL/6J	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:105043	Ahr	"Ahr<tm1Yfk>/Ahr<tm1Yfk>,Nfe2l2<tm1Mym>/Nfe2l2<tm1Mym>"	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J * ICR	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000470	abnormal stomach morphology	CCO:MP0000470
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:105043	Ahr	Ahr<tm2Bra>/Ahr<tm2Bra>	involves: 129/Sv * C57BL/6	MP:0004004	patent ductus venosus	CCO:MP0004004
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003402	decreased liver weight	CCO:MP0003402
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0001263	weight loss	CCO:MP0001263
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000377	abnormal hair follicle morphology	CCO:MP0000377
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000376	folliculitis	CCO:MP0000376
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0002083	premature death	CCO:MP0002083
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005141	liver hyperplasia	CCO:MP0005141
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000367	abnormal coat/ hair morphology	CCO:MP0000367
MGI:105043	Ahr	Ahr<tm1Gonz>/Ahr<tm1Gonz>	involves: 129S4/SvJae * C57BL/6N	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:105043	Ahr	Ahr<tm1Bra>/Ahr<tm1Bra>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000601	small liver	CCO:MP0000601
MGI:105043	Ahr	Ahr<tm3Bra>/Ahr<tm3Bra>	involves: 129/Sv * C57BL/6J * DBA/2	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	Ahr<tm3Bra>/Ahr<tm3Bra>	involves: 129/Sv * C57BL/6J * DBA/2	MP:0004004	patent ductus venosus	CCO:MP0004004
MGI:105043	Ahr	"Ahr<tm3.1Bra>/Ahr<tm3.1Bra>,Tg(Alb-cre)21Mgn/0"	B6.Cg-Ahr<tm3.1Bra> Tg(Alb-cre)21Mgn	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:105043	Ahr	"Ahr<tm3.1Bra>/Ahr<tm3.1Bra>,Tg(Tek-cre)12Flv/0"	B6.Cg-Ahr<tm3.1Bra> Tg(Tek-cre)12Flv	MP:0004004	patent ductus venosus	CCO:MP0004004
MGI:87977	Ak1	"Ak1<tm1Bew>/Ak1<tm1Bew>,Ckm<tm1Bew>/Ckm<tm1Bew>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0005620	abnormal muscle contractility	CCO:MP0005620
MGI:87977	Ak1	"Ak1<tm1Bew>/Ak1<tm1Bew>,Ckm<tm1Bew>/Ckm<tm1Bew>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0003806	abnormal nucleotide metabolism	CCO:MP0003806
MGI:87977	Ak1	"Ak1<tm1Bew>/Ak1<tm1Bew>,Ckm<tm1Bew>/Ckm<tm1Bew>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0002954	abnormal aerobic energy metabolism	CCO:MP0002954
MGI:87977	Ak1	Ak1<tm1Bew>/Ak1<tm1Bew>	involves: 129P2/OlaHsd * C57BL/6	MP:0003806	abnormal nucleotide metabolism	CCO:MP0003806
MGI:87977	Ak1	Ak1<tm1Bew>/Ak1<tm1Bew>	involves: 129P2/OlaHsd * C57BL/6	MP:0000343	altered response to myocardial infarction	CCO:MP0000343
MGI:87977	Ak1	Ak1<tm1Bew>/Ak1<tm1Bew>	involves: 129P2/OlaHsd * C57BL/6	MP:0002954	abnormal aerobic energy metabolism	CCO:MP0002954
MGI:87977	Ak1	Ak1<tm1Bew>/Ak1<tm1Bew>	involves: 129P2/OlaHsd * C57BL/6	MP:0005450	abnormal energy expenditure	CCO:MP0005450
MGI:87977	Ak1	Ak1<tm1Bew>/Ak1<tm1Bew>	involves: 129P2/OlaHsd * C57BL/6	MP:0002106	abnormal muscle physiology	CCO:MP0002106
MGI:87977	Ak1	Ak1<tm1Bew>/Ak1<tm1Bew>	involves: 129P2/OlaHsd * C57BL/6	MP:0002078	abnormal glucose homeostasis	CCO:MP0002078
MGI:1928488	Akap8	"Akap8<Gt(XG068)Byg>/Akap8<Gt(XG068)Byg>,Fign<fi>/Fign<+>"	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:1928488	Akap8	"Akap8<Gt(XG068)Byg>/Akap8<Gt(XG068)Byg>,Fign<fi>/Fign<fi>"	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	MP:0001575	cyanosis	CCO:MP0001575
MGI:1928488	Akap8	"Akap8<Gt(XG068)Byg>/Akap8<Gt(XG068)Byg>,Fign<fi>/Fign<fi>"	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1928488	Akap8	"Akap8<Gt(XG068)Byg>/Akap8<Gt(XG068)Byg>,Fign<fi>/Fign<fi>"	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1928488	Akap8	"Akap8<Gt(XG068)Byg>/Akap8<+>,Fign<fi>/Fign<fi>"	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:1928488	Akap8	"Akap8<Gt(XG068)Byg>/Akap8<Gt(XG068)Byg>,Fign<fi>/Fign<fi>"	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:1928488	Akap8	Akap8<Gt(XG068)Byg>/Akap8<Gt(XG068)Byg>	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1928488	Akap8	"Akap8<Gt(XG068)Byg>/Akap8<Gt(XG068)Byg>,Fign<fi>/Fign<fi>"	involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm1Kna>,Tg(Ttr-cre/Esr1)1Vco/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005344	increased circulating bilirubin level	CCO:MP0005344
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005439	decreased glycogen level	CCO:MP0005439
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002874	decreased hemoglobin content	CCO:MP0002874
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0003326	liver failure	CCO:MP0003326
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm1Kna>,Tg(Ttr-cre/Esr1)1Vco/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0002083	premature death	CCO:MP0002083
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002397	abnormal bone marrow morphology	CCO:MP0002397
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm1Kna>,Tg(Ttr-cre/Esr1)1Vco/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0003326	liver failure	CCO:MP0003326
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm1Kna>,Tg(Ttr-cre/Esr1)1Vco/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0003893	increased hepatocyte proliferation	CCO:MP0003893
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0003893	increased hepatocyte proliferation	CCO:MP0003893
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000609	abnormal liver physiology	CCO:MP0000609
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:2139135	Anapc2	Anapc2<tm2Kna>/Anapc2<tm2Kna>	involves: 129P2/OlaHsd * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005319	abnormal enzyme/ coenzyme level	CCO:MP0005319
MGI:2139135	Anapc2	"Anapc2<tm1Kna>/Anapc2<tm2Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001577	anemia	CCO:MP0001577
MGI:96819	Anxa1	Anxa1<tm1Rjf>/Anxa1<tm1Rjf>	Not Specified	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:96819	Anxa1	Anxa1<tm1Rjf>/Anxa1<tm1Rjf>	Not Specified	MP:0001798	impaired macrophage phagocytosis	CCO:MP0001798
MGI:96819	Anxa1	Anxa1<tm1Rjf>/Anxa1<tm1Rjf>	Not Specified	MP:0002442	abnormal leukocyte physiology	CCO:MP0002442
MGI:96819	Anxa1	Anxa1<tm1Rjf>/Anxa1<+>	Not Specified	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000798	abnormal frontal lobe morphology	CCO:MP0000798
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<+>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0009026	abnormal brain pia mater morphology	CCO:MP0009026
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0003651	abnormal axon outgrowth	CCO:MP0003651
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0005623	abnormal meninges morphology	CCO:MP0005623
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000794	abnormal parietal lobe morphology	CCO:MP0000794
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002196	absent corpus callosum	CCO:MP0002196
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000792	abnormal cortical marginal zone morphology	CCO:MP0000792
MGI:107765	Apbb1	Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>	involves: 129S6/SvEvTac * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:107765	Apbb1	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000812	abnormal dentate gyrus morphology	CCO:MP0000812
MGI:107765	Apbb1	Apbb1<tm1Trus>/Apbb1<tm1Trus>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:107765	Apbb1	Apbb1<tm1Trus>/Apbb1<tm1Trus>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:107765	Apbb1	Apbb1<tm1Quhu>/Apbb1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002799	abnormal passive avoidance behavior	CCO:MP0002799
MGI:107765	Apbb1	Apbb1<tm1Quhu>/Apbb1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:107765	Apbb1	Apbb1<tm1Quhu>/Apbb1<tm1Quhu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002799	abnormal passive avoidance behavior	CCO:MP0002799
MGI:107765	Apbb1	Apbb1<tm1Quhu>/Apbb1<tm1Quhu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002196	absent corpus callosum	CCO:MP0002196
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0003651	abnormal axon outgrowth	CCO:MP0003651
MGI:108405	Apbb2	Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>	involves: 129S6/SvEvTac * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000798	abnormal frontal lobe morphology	CCO:MP0000798
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000794	abnormal parietal lobe morphology	CCO:MP0000794
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000812	abnormal dentate gyrus morphology	CCO:MP0000812
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0005623	abnormal meninges morphology	CCO:MP0005623
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000792	abnormal cortical marginal zone morphology	CCO:MP0000792
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0009026	abnormal brain pia mater morphology	CCO:MP0009026
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<+>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:108405	Apbb2	"Apbb1<tm1Sgnt>/Apbb1<tm1Sgnt>,Apbb2<tm1Sgnt>/Apbb2<tm1Sgnt>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0001282	short vibrissae	CCO:MP0001282
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0001263	weight loss	CCO:MP0001263
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000619	salivary gland epithelial hyperplasia	CCO:MP0000619
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000377	abnormal hair follicle morphology	CCO:MP0000377
MGI:88039	Apc	"Apc<Min>/Apc<Min>,Ppard<tm1.1Rev>/Ppard<tm1.1Rev>"	involves: C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<Min>/Apc<Min>,Ppard<tm1.1Rev>/Ppard<tm1.1Rev>"	involves: C57BL/6J	MP:0003269	colonic polyps	CCO:MP0003269
MGI:88039	Apc	"Apc<Min>/Apc<Min>,Ppard<tm1.1Rev>/Ppard<tm1.1Rev>"	involves: C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0002095	abnormal skin pigmentation	CCO:MP0002095
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0001344	blepharoptosis	CCO:MP0001344
MGI:88039	Apc	Apc<tm2Rak>/Apc<tm2.1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:88039	Apc	Apc<tm2.1Rak>/Apc<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0003293	rectal hemorrhage	CCO:MP0003293
MGI:88039	Apc	Apc<tm2.1Rak>/Apc<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0001265	decreased body size	CCO:MP0001265
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000706	small thymus	CCO:MP0000706
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0009539	abnormal Hassall's corpuscle morphology	CCO:MP0009539
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0003704	abnormal hair follicle development	CCO:MP0003704
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0006000	abnormal corneal epithelium morphology	CCO:MP0006000
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0002820	abnormal premaxilla morphology	CCO:MP0002820
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0005248	abnormal Harderian gland morphology	CCO:MP0005248
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0005202	lethargy	CCO:MP0005202
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0002691	small stomach	CCO:MP0002691
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0001210	thick skin ridges	CCO:MP0001210
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000422	delayed hair appearance	CCO:MP0000422
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000124	absent teeth	CCO:MP0000124
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000022	abnormal ear shape	CCO:MP0000022
MGI:88039	Apc	"Cdx2<tm1Mmt>/Cdx2<+>,Apc<tm1Mmt>/Apc<+>"	B6.129-Cdx2<tm1Mmt> Apc<tm1Mmt>	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0001211	wrinkled skin	CCO:MP0001211
MGI:88039	Apc	Apc<tm2.1Rak>/Apc<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0001192	scaly skin	CCO:MP0001192
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000703	abnormal thymus morphology	CCO:MP0000703
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0002656	abnormal keratinocyte differentiation	CCO:MP0002656
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Mbd4<tm1Wed>/Mbd4<tm1Wed>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Cdx2<tm1Mmt>/Cdx2<+>,Apc<tm1Mmt>/Apc<+>"	B6.129-Cdx2<tm1Mmt> Apc<tm1Mmt>	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tg(CAG-PGDS)S-55Hjl/0"	involves: C57BL/6J * FVB/N	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Ptgds2<tm1Hjl>/Ptgds2<tm1Hjl>"	involves: 129 * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Ptgds2<tm1Hjl>/Ptgds2<+>"	involves: 129 * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Ptgds<tm1Ohy>/Ptgds<tm1Ohy>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mbd4<tm1Bird>/Mbd4<tm1Bird>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Cdx2<tm1Mmt>/Cdx2<+>,Apc<tm1Mmt>/Apc<+>"	B6.129-Cdx2<tm1Mmt> Apc<tm1Mmt>	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mbd4<tm1Bird>/Mbd4<tm1Bird>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:88039	Apc	"Cdx2<tm1Mmt>/Cdx2<+>,Apc<tm1Mmt>/Apc<+>"	B6.129-Cdx2<tm1Mmt> Apc<tm1Mmt>	MP:0000495	abnormal colon morphology	CCO:MP0000495
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Mbd4<tm1Wed>/Mbd4<tm1Wed>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * SJL	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:88039	Apc	"Apc<Min>/Apc<+>,Atp5a1<Mom2-C57BL/6J>/Atp5a1<Mom2-C57BL/6J>"	involves: C57BL/6J * DBA/2J	MP:0005514	increased resistance to tumor development	CCO:MP0005514
MGI:88039	Apc	"Apc<Min>/Apc<+>,Atp5a1<Mom2-C57BL/6J>/Atp5a1<+>"	involves: C57BL/6J * DBA/2J	MP:0005514	increased resistance to tumor development	CCO:MP0005514
MGI:88039	Apc	"Apc<Min>/Apc<Min>,H19<tm1Rohl>/H19<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<Min>,H19<tm1Rohl>/H19<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:88039	Apc	"Apc<Min>/Apc<Min>,H19<tm1Rohl>/H19<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000490	abnormal crypts of Lieberkuhn morphology	CCO:MP0000490
MGI:88039	Apc	"Apc<Min>/Apc<+>,Egfr<Wa5>/Egfr<+>"	involves: BALB/cAnN * C3H/HeN * C57BL/6J	MP:0005514	increased resistance to tumor development	CCO:MP0005514
MGI:88039	Apc	"Apc<Min>/Apc<Min>,Sat1<tm1Alh>/Y"	involves: 129X1/SvJ * C57BL/6J	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	Apc<tm2.1Rak>/Apc<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	Apc<tm2.1Rak>/Apc<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0003269	colonic polyps	CCO:MP0003269
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0006079	stomach tumor	CCO:MP0006079
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000417	short hair	CCO:MP0000417
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mbd4<tm1Bird>/Mbd4<tm1Bird>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0000465	gastrointestinal hemorrhage	CCO:MP0000465
MGI:88039	Apc	Apc<tm2.1Rak>/Apc<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0001382	abnormal nursing	CCO:MP0001382
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0000490	abnormal crypts of Lieberkuhn morphology	CCO:MP0000490
MGI:88039	Apc	Apc<tm1Hsa>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0000462	abnormal digestive system morphology	CCO:MP0000462
MGI:88039	Apc	Apc<tm1Hsa>/Apc<tm1Hsa>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:88039	Apc	"Cdx2<tm1Mmt>/Cdx2<+>,Apc<tm1Mmt>/Apc<+>"	B6.129-Cdx2<tm1Mmt> Apc<tm1Mmt>	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:88039	Apc	"Cdx2<tm1Mmt>/Cdx2<+>,Apc<tm1Mmt>/Apc<+>"	B6.129-Cdx2<tm1Mmt> Apc<tm1Mmt>	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:88039	Apc	"Cdx2<tm1Mmt>/Cdx2<+>,Apc<tm1Mmt>/Apc<+>"	B6.129-Cdx2<tm1Mmt> Apc<tm1Mmt>	MP:0003269	colonic polyps	CCO:MP0003269
MGI:88039	Apc	"Apc<Min>/Apc<+>,Dnmt3b<tm1Jae>/Dnmt3b<tm1Jae>,Tg(Fabp1-cre)1Jig/0"	involves: 129 * C57BL/6 * C57BL/6J * FVB/N	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:88039	Apc	"Apc<tm2Rak>/Apc<tm2Rak>,Tg(KRT14-cre)8Brn/0"	involves: 129/Sv * C57BL/6J * FVB/N * SJL	MP:0000116	abnormal tooth development	CCO:MP0000116
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<tm1Ddr>"	involves: C57BL/6J	MP:0000488	abnormal intestinal epithelium morphology	CCO:MP0000488
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0004833	ovary atrophy	CCO:MP0004833
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006079	stomach tumor	CCO:MP0006079
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Cdh1<tm1Cbm>/Cdh1<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0006079	stomach tumor	CCO:MP0006079
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Cdh1<tm1Cbm>/Cdh1<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Pten<tm2Mak>/Pten<tm2Mak>,Tg(Cyp1a1-cre/ERT)1Dwi/0"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA	MP:0003303	peritoneal inflammation	CCO:MP0003303
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Pten<tm2Mak>/Pten<tm2Mak>,Tg(Cyp1a1-cre/ERT)1Dwi/0"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0004894	uterus atrophy	CCO:MP0004894
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<tm1Ddr>"	involves: C57BL/6J	MP:0000490	abnormal crypts of Lieberkuhn morphology	CCO:MP0000490
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001140	abnormal vagina epithelium morphology	CCO:MP0001140
MGI:88039	Apc	Apc<tm1Rfo>/Apc<tm1Rfo>	B6.129P2-Apc<tm1Rfo>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001132	absent mature ovarian follicles	CCO:MP0001132
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tg(Rorc-EGFP)1Ebe/?"	involves: C57BL/6	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Pten<tm2Mak>/Pten<tm2Mak>,Tg(Cyp1a1-cre/ERT)1Dwi/0"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	Apc<tm3Mmt>/Apc<+>	involves: 129X1/SvJ * C57BL/6N	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Pten<tm2Mak>/Pten<tm2Mak>,Tg(Cyp1a1-cre/ERT)1Dwi/0"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<tm1Ddr>"	involves: C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0000639	abnormal adrenal gland morphology	CCO:MP0000639
MGI:88039	Apc	"Apc<Min>/Apc<+>,Slc5a8<tm1.1Boet>/Slc5a8<tm1.1Boet>"	involves: C57BL/6 * C57BL/6J	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<tm1Ddr>"	involves: C57BL/6J	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:88039	Apc	Apc<tm2Mmt>/Apc<+>	involves: 129X1/SvJ	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:88039	Apc	Apc<tm2Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:88039	Apc	Apc<tm2Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0003085	abnormal egg cylinder morphology	CCO:MP0003085
MGI:88039	Apc	"Apc<Min>/Apc<+>,Myc<tm1Jlc>/Myc<+>"	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	MP:0001663	abnormal digestive system physiology	CCO:MP0001663
MGI:88039	Apc	"Apc<Min>/Apc<+>,Myc<tm1Jlc>/Myc<+>"	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	MP:0002396	abnormal hematopoietic system morphology/development	CCO:MP0002396
MGI:88039	Apc	"Apc<Min>/Apc<+>,Myc<tm1Jlc>/Myc<+>"	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: C57BL/6 * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: C57BL/6 * C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	Apc<tm2Mmt>/Apc<tm2Mmt>	involves: 129X1/SvJ	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<tm1Ddr>"	involves: C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tg(Rorc-EGFP)1Ebe/?"	involves: C57BL/6	MP:0008466	enlarged mesenteric lymph nodes	CCO:MP0008466
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Smad2<tm1Kato>/Smad2<+>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tg(Rorc-EGFP)1Ebe/?"	involves: C57BL/6	MP:0003269	colonic polyps	CCO:MP0003269
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tg(Rorc-EGFP)1Ebe/?"	involves: C57BL/6	MP:0002435	abnormal effector T cell morphology	CCO:MP0002435
MGI:88039	Apc	Apc<tm1.1Tno>/Apc<+>	involves: 129S4/SvJae * C57BL/6	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<tm1.1Tno>/Apc<+>	involves: 129S4/SvJae * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:88039	Apc	Apc<tm1.1Tno>/Apc<+>	involves: 129S4/SvJae * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0000639	abnormal adrenal gland morphology	CCO:MP0000639
MGI:88039	Apc	"Apc<Min>/Apc<+>,Foxl1<tm1Khk>/Foxl1<tm1Khk>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Apc<Min>/Apc<+>,Foxl1<tm1Khk>/Foxl1<tm1Khk>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:88039	Apc	"Apc<Min>/Apc<+>,Foxl1<tm1Khk>/Foxl1<tm1Khk>"	involves: 129P2/OlaHsd * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:88039	Apc	"Apc<Min>/Apc<+>,Foxl1<tm1Khk>/Foxl1<tm1Khk>"	involves: 129P2/OlaHsd * C57BL/6	MP:0006079	stomach tumor	CCO:MP0006079
MGI:88039	Apc	"Apc<Min>/Apc<+>,Foxl1<tm1Khk>/Foxl1<tm1Khk>"	involves: 129P2/OlaHsd * C57BL/6	MP:0003299	gastric polyps	CCO:MP0003299
MGI:88039	Apc	Apc<tm1.1Tno>/Apc<+>	involves: 129S4/SvJae * C57BL/6	MP:0003270	intestinal obstruction	CCO:MP0003270
MGI:88039	Apc	"Apc<Min>/Apc<+>,Foxl1<tm1Khk>/Foxl1<tm1Khk>"	involves: 129P2/OlaHsd * C57BL/6	MP:0003269	colonic polyps	CCO:MP0003269
MGI:88039	Apc	Apc<tm1.1Tno>/Apc<+>	involves: 129S4/SvJae * C57BL/6	MP:0000465	gastrointestinal hemorrhage	CCO:MP0000465
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	B6.129P2-Apc<tm1Rak>	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:88039	Apc	"Apc<Min>/Apc<+>,Nos2<tm1Lau>/Nos2<tm1Lau>"	B6.Cg-Nos2<tm1Lau> Apc<Min>	MP:0003447	decreased tumor growth/size	CCO:MP0003447
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mmom1<C57BL/6J>/Mmom1<FVB/NTac>"	involves: C57BL/6J * FVB/NTac	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<+>"	involves: C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tgfbr1<tm1Bopa>/Tgfbr1<+>"	B6.Cg-Tgfbr1<tm1Bopa> Apc<Min>	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tgfbr1<tm1Bopa>/Tgfbr1<+>"	B6.Cg-Tgfbr1<tm1Bopa> Apc<Min>	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tgfbr1<tm1Bopa>/Tgfbr1<+>"	involves: 129S1/SvImJ * C57BL/6J	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tgfbr1<tm1Bopa>/Tgfbr1<+>"	involves: 129S1/SvImJ * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	B6.129P2-Apc<tm1Rak>	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	B6.129P2-Apc<tm1Rak>	MP:0003269	colonic polyps	CCO:MP0003269
MGI:88039	Apc	"Apc<Min>/Apc<+>,Ptprh<tm1.1Mato>/Ptprh<tm1.1Mato>"	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0002053	decreased incidence of induced tumors	CCO:MP0002053
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<+>"	involves: C57BL/6J	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:88039	Apc	"Apc<Min>/Apc<+>,Nos2<tm1Lau>/Nos2<+>"	B6.Cg-Nos2<tm1Lau> Apc<Min>	MP:0003447	decreased tumor growth/size	CCO:MP0003447
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	B6.129P2-Apc<tm1Rak>	MP:0003299	gastric polyps	CCO:MP0003299
MGI:88039	Apc	"Apc<Min>/Apc<+>,Nos2<tm1Lau>/Nos2<+>"	B6.Cg-Nos2<tm1Lau> Apc<Min>	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> +/+ Smad4<E6sad>	MP:0003299	gastric polyps	CCO:MP0003299
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> +/+ Smad4<E6sad>	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> +/+ Smad4<E6sad>	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> +/+ Smad4<E6sad>	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> Smad4<E6sad>/+ +	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> Smad4<E6sad>/+ +	MP:0003299	gastric polyps	CCO:MP0003299
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> Smad4<E6sad>/+ +	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> Smad4<E6sad>/+ +	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> Smad4<E6sad>/+ +	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Smad4<E6sad>/Smad4<+>"	B6.129P2-Apc<tm1Rak> Smad4<E6sad>/+ +	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<tm1.1Tno>/Apc<+>,Ctnna1<del>/Ctnna1<+>"	involves: 129S4/SvJae * C57BL/6	MP:0003171	phenotypic reversion	CCO:MP0003171
MGI:88039	Apc	Apc<tm1.1Tno>/Apc<+>	involves: 129S4/SvJae * C57BL/6	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<+>"	involves: C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<Min>/Apc<+>,Tgfbr1<tm1Bopa>/Tgfbr1<+>"	involves: 129S1/SvImJ * C57BL/6J	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:88039	Apc	"Apc<Min>/Apc<+>,Nos2<tm1Lau>/Nos2<tm1Lau>"	B6.Cg-Nos2<tm1Lau> Apc<Min>	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001132	absent mature ovarian follicles	CCO:MP0001132
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Smad2<tm2Kato>/Smad2<+>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001140	abnormal vagina epithelium morphology	CCO:MP0001140
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Smad2<tm1Kato>/Smad2<+>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0004833	ovary atrophy	CCO:MP0004833
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mmom1<C57BL/6J>/Mmom1<FVB/NTac>,Mmom3<C57BL/6J>/Mmom3<FVB/NTac>"	involves: C57BL/6J * FVB/NTac	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mmom2<C57BL/6J>/Mmom2<FVB/NTac>"	involves: C57BL/6J * FVB/NTac	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mmom2<129X1/SvJ>/Mmom2<C57BL/6J>"	involves: 129X1/SvJ * C57BL/6J	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mmom2<C57BL/6J>/Mmom2<FVB/NTac>,Mmom3<C57BL/6J>/Mmom3<FVB/NTac>"	involves: C57BL/6J * FVB/NTac	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mmom2<C57BL/6J>/Mmom2<FVB/NTac>,Mmom4<C57BL/6J>/Mmom4<FVB/NTac>"	involves: C57BL/6J * FVB/NTac	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mmom4<C57BL/6J>/Mmom4<FVB/NTac>"	involves: C57BL/6J * FVB/NTac	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Smad2<tm2Kato>/Smad2<+>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0004894	uterus atrophy	CCO:MP0004894
MGI:88039	Apc	Apc<Min>/Apc<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:88039	Apc	"Apc<tm2.1Cip>/Apc<+>,Tg(Fabp1-cre)1Jig/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<tm2.1Cip>/Apc<+>,Kras<tm4Tyj>/Kras<+>,Tg(Fabp1-cre)1Jig/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<tm2.1Cip>/Apc<+>,Kras<tm4Tyj>/Kras<+>,Tg(Fabp1-cre)1Jig/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<+>"	involves: C57BL/6J	MP:0000488	abnormal intestinal epithelium morphology	CCO:MP0000488
MGI:88039	Apc	"Apc<Min>/Apc<+>,Glp2r<tm1Ddr>/Glp2r<+>"	involves: C57BL/6J	MP:0000490	abnormal crypts of Lieberkuhn morphology	CCO:MP0000490
MGI:88039	Apc	"Apc<Min>/Apc<+>,Dnmt1<tm1Pwl>/Dnmt1<+>"	involves: 129S4/SvJae * C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<tm1Tno>/Apc<tm1Tno>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0003270	intestinal obstruction	CCO:MP0003270
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0000493	rectal prolapse	CCO:MP0000493
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002113	abnormal skeleton development	CCO:MP0002113
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000438	abnormal skull morphology	CCO:MP0000438
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:88039	Apc	"Apc<tm1Tno>/Apc<tm1Tno>,Tg(CDX2-cre*)189Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88039	Apc	"Apc<Min>/Apc<+>,Dnmt1<tm1Jae>/Dnmt1<+>"	involves: 129S4/SvJae * C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(Vil-cre)997Gum/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(CDX2-cre)101Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<tm1Tno>/Apc<tm1Tno>,Tg(CDX2-cre*)189Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<tm1Tno>/Apc<tm1Tno>,Tg(CDX2-cre*)189Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:88039	Apc	"Apc<tm1Tno>/Apc<tm1Tno>,Tg(CDX2-cre*)189Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0000592	short tail	CCO:MP0000592
MGI:88039	Apc	"Apc<tm1Tno>/Apc<tm1Tno>,Tg(CDX2-cre*)189Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0000585	kinked tail	CCO:MP0000585
MGI:88039	Apc	"Apc<tm1Tno>/Apc<tm1Tno>,Tg(CDX2-cre*)189Erf/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<tm1Ecrm>/Apc<tm1Ecrm>	involves: 129P2/OlaHsd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000158	absent sternum	CCO:MP0000158
MGI:88039	Apc	Apc<tm1.1Ecrm>/Apc<+>	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0008395	abnormal osteoblast differentiation	CCO:MP0008395
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0008272	abnormal endochondral bone ossification	CCO:MP0008272
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0004733	abnormal thoracic cavity	CCO:MP0004733
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0004672	short ribs	CCO:MP0004672
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0004344	scapular bone hypoplasia	CCO:MP0004344
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006279	abnormal limb development	CCO:MP0006279
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0003257	abnormal abdominal wall	CCO:MP0003257
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(Vil-cre)997Gum/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005296	abnormal humerus morphology	CCO:MP0005296
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(Vil-cre)997Gum/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001208	blistering	CCO:MP0001208
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000556	abnormal hindlimb morphology	CCO:MP0000556
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001258	decreased body length	CCO:MP0001258
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000458	abnormal mandible morphology	CCO:MP0000458
MGI:88039	Apc	"Apc<tm1Tno>/Apc<tm1Tno>,Tg(Vil-cre)997Gum/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:88039	Apc	"Apc<tm1Tno>/Apc<+>,Tg(Vil-cre)997Gum/0"	involves: 129S4/SvJae * C57BL/6 * SJL	MP:0009309	small intestine adenocarcinoma	CCO:MP0009309
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:88039	Apc	"Fen1<tm1Rak>/Fen1<+>,Apc<tm1Rak>/Apc<+>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * SJL/J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:88039	Apc	"Apc<tm1Cip>/Apc<+>,H19<tm1Lda>/H19<+>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002815	adenoma	CCO:MP0002815
MGI:88039	Apc	"Apc<tm1Ecrm>/Apc<tm1Ecrm>,Tg(Col2a1-cre)1Rsjo/0"	involves: 129P2/OlaHsd * FVB/N	MP:0000164	abnormal cartilage development	CCO:MP0000164
MGI:88039	Apc	"Fen1<tm1Rak>/Fen1<+>,Apc<tm1Rak>/Apc<+>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * SJL/J	MP:0002018	malignant tumors	CCO:MP0002018
MGI:88039	Apc	"Apc<tm1Cip>/Apc<+>,H19<tm1Lda>/H19<+>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * CBA	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Fen1<tm1Rak>/Fen1<+>,Apc<tm1Rak>/Apc<+>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * SJL/J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Apc<tm1Cip>/Apc<+>,H19<tm1Lda>/H19<+>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * CBA	MP:0003269	colonic polyps	CCO:MP0003269
MGI:88039	Apc	"Fen1<tm1Rak>/Fen1<+>,Apc<tm1Rak>/Apc<+>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * SJL/J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<tm1Cip>/Apc<+>,H19<tm1Lda>/H19<+>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * CBA	MP:0002815	adenoma	CCO:MP0002815
MGI:88039	Apc	Apc<tm1Mmt>/Apc<tm1Mmt>	involves: 129S2/SvPas * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0003293	rectal hemorrhage	CCO:MP0003293
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: AKR/J * C57BL/6J	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<tm1Rak>/Apc<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: AKR/J * C57BL/6J	MP:0003292	melena	CCO:MP0003292
MGI:88039	Apc	Apc<tm1Mmt>/Apc<+>	involves: 129S2/SvPas * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: AKR/J * C57BL/6J	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: AKR/J * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: AKR/J * C57BL/6J	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	Apc<tm1Rak>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:88039	Apc	Apc<tm1Mmt>/Apc<+>	involves: 129S2/SvPas * C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	Apc<tm1Rfo>/Apc<tm1Rfo>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:88039	Apc	Apc<tm1Rfo>/Apc<tm1Rfo>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001247	dermal cysts	CCO:MP0001247
MGI:88039	Apc	Apc<tm1Rfo>/Apc<tm1Rfo>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:88039	Apc	Apc<tm1Rfo>/Apc<tm1Rfo>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006401	absent preputial gland	CCO:MP0006401
MGI:88039	Apc	Apc<tm1Tno>/Apc<tm1Tno>	involves: 129S4/SvJae * C57BL/6	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Smad4<tm1Mmt>/Smad4<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Smad4<tm1Mmt>/Smad4<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Smad4<tm1Mmt>/Smad4<+>"	involves: 129S2/SvPas * C57BL/6	MP:0003414	epidermal cyst	CCO:MP0003414
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Smad4<tm1Mmt>/Smad4<+>"	involves: 129S2/SvPas * C57BL/6	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:88039	Apc	"Apc<Min>/Apc<+>,Dcc<tm1Wbg>/Dcc<+>"	involves: C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<Min>,Asph<tm1Jed>/Asph<tm1Jed>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J * C57BL/6NTac	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: AKR/J * C57BL/6J	MP:0001548	hyperlipidemia	CCO:MP0001548
MGI:88039	Apc	"Apc<tm1Rak>/Apc<+>,Hmmr<tm1Baa>/Hmmr<tm1Baa>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:88039	Apc	Apc<tm2Tno>/Apc<+>	Not Specified	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mmp7<tm1Lmm>/Mmp7<tm1Lmm>"	involves: C57BL/6 * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Apc<Min>/Apc<+>,Thbs1<tm1Hyn>/Thbs1<tm1Hyn>"	involves: C57BL/6J	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	"Apc<Min>/Apc<Min>,Asph<tm1Jed>/Asph<tm1Jed>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J * C57BL/6NTac	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<Min>/Apc<+>,Thbs1<tm1Hyn>/Thbs1<tm1Hyn>"	involves: C57BL/6J	MP:0002815	adenoma	CCO:MP0002815
MGI:88039	Apc	"Apc<Min>/Apc<+>,Thbs1<tm1Hyn>/Thbs1<tm1Hyn>"	involves: C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:88039	Apc	"Apc<Min>/Apc<+>,Thbs1<tm1Hyn>/Thbs1<tm1Hyn>"	involves: C57BL/6J	MP:0000162	lordosis	CCO:MP0000162
MGI:88039	Apc	"Apc<Min>/Apc<+>,Thbs1<tm1Hyn>/Thbs1<tm1Hyn>"	involves: C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	"Apc<Min>/Apc<+>,Thbs1<tm1Hyn>/Thbs1<tm1Hyn>"	involves: C57BL/6J	MP:0001263	weight loss	CCO:MP0001263
MGI:88039	Apc	"Apc<Min>/Apc<+>,Thbs1<tm1Hyn>/Thbs1<tm1Hyn>"	involves: C57BL/6J	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:88039	Apc	"Apc<Min>/Apc<+>,Thbs1<tm1Hyn>/Thbs1<tm1Hyn>"	involves: C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Ptgs2<tm1Jed>/Ptgs2<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mbd2<tm1Bh>/Mbd2<+>"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mbd2<tm1Bh>/Mbd2<+>"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mbd2<tm1Bh>/Mbd2<tm1Bh>"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	MP:0003447	decreased tumor growth/size	CCO:MP0003447
MGI:88039	Apc	"Apc<Min>/Apc<+>,Mbd2<tm1Bh>/Mbd2<tm1Bh>"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:88039	Apc	"Apc<tm1Kk>/Apc<tm1Kk>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:88039	Apc	"Apc<tm1Kk>/Apc<tm1Kk>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0001825	arrested T cell differentiation	CCO:MP0001825
MGI:88039	Apc	Apc<tm3Mmt>/Apc<+>	B6.129X1-Apc<tm3Mmt>	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Recql4<tm1Glu>/Recql4<tm1Glu>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:88039	Apc	"Apc<Min>/Apc<+>,Recql4<tm1Glu>/Recql4<tm1Glu>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002815	adenoma	CCO:MP0002815
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: C57BL/6J	MP:0000493	rectal prolapse	CCO:MP0000493
MGI:88039	Apc	"Apc<tm1Kk>/Apc<tm1Kk>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:88039	Apc	"Apc<Min>/Apc<+>,Recql4<tm1Glu>/Recql4<tm1Glu>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Nkd1<tm1Tko>/Nkd1<tm1Tko>"	involves: 129X1/SvJ	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:88039	Apc	Apc<tm2.1Cip>/Apc<tm2.1Cip>	involves: 129P2/OlaHsd * C57BL/6N	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:88039	Apc	Apc<tm4Mmt>/Apc<tm4Mmt>	B6.129X1-Apc<tm4Mmt>	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:88039	Apc	"Apc<Min>/Apc<+>,Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>"	involves: C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<tm1Kk>/Apc<tm1Kk>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:88039	Apc	Apc<tm4Mmt>/Apc<+>	B6.129X1-Apc<tm4Mmt>	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	Apc<tm4Mmt>/Apc<+>	B6.129X1-Apc<tm4Mmt>	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<tm2.1Cip>/Apc<tm2.1Cip>	involves: 129P2/OlaHsd * C57BL/6N	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:88039	Apc	Apc<tm2.1Cip>/Apc<tm2.1Cip>	involves: 129P2/OlaHsd * C57BL/6N	MP:0005141	liver hyperplasia	CCO:MP0005141
MGI:88039	Apc	"Apc<Min>/Apc<+>,Hp<tm1Skl>/Hp<tm1Skl>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0000474	abnormal foregut morphology	CCO:MP0000474
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0005221	abnormal rostral-caudal axis patterning	CCO:MP0005221
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0001701	incomplete embryo turning	CCO:MP0001701
MGI:88039	Apc	"Apc<Min>/Apc<+>,Blm<tm1Grdn>/Blm<+>"	involves: 129P2/OlaHsd * 129S/SvEv * Black Swiss * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0000925	abnormal floor plate morphology	CCO:MP0000925
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Ptgs2<tm1Jed>/Ptgs2<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003269	colonic polyps	CCO:MP0003269
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0000270	abnormal heart tube morphology	CCO:MP0000270
MGI:88039	Apc	Apc<tm3Mmt>/Apc<+>	B6.129X1-Apc<tm3Mmt>	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0001685	abnormal endoderm development	CCO:MP0001685
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0003232	abnormal forebrain development	CCO:MP0003232
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:88039	Apc	"Apc<Min>/Apc<+>,Blm<tm1Grdn>/Blm<+>"	involves: 129P2/OlaHsd * 129S/SvEv * Black Swiss * C57BL/6J	MP:0002815	adenoma	CCO:MP0002815
MGI:88039	Apc	"Apc<Min>/Apc<+>,Ppard<tm1Jps>/Ppard<tm1Jps>"	involves: 129/Sv * AKR/J * C57BL/6 * C57BL/6J	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:88039	Apc	"Apc<Min>/Apc<+>,Ppard<tm1Jps>/Ppard<tm1Jps>"	involves: 129/Sv * AKR/J * C57BL/6 * C57BL/6J	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	"Apc<Min>/Apc<+>,Zbtb33<tm1.1Bird>/Y"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	"Apc<Min>/Apc<+>,Zbtb33<tm1.1Bird>/Y"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	"Apc<Min>/Apc<+>,Zbtb33<tm1.1Bird>/Y"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J	MP:0003447	decreased tumor growth/size	CCO:MP0003447
MGI:88039	Apc	"Apc<tm1Kk>/Apc<tm1Kk>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0000706	small thymus	CCO:MP0000706
MGI:88039	Apc	Apc<tm1Cip>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:88039	Apc	"Apc<tm1Mmt>/Apc<+>,Ptgs2<tm1Jed>/Ptgs2<tm1Jed>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: C57BL/6J	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:88039	Apc	Apc<Min>/Apc<+>	involves: C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<tm1Cip>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0003293	rectal hemorrhage	CCO:MP0003293
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0004713	split notochord	CCO:MP0004713
MGI:88039	Apc	Apc<tm1Cip>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0005657	abnormal neural plate morphology	CCO:MP0005657
MGI:88039	Apc	Apc<tm1Cip>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0000493	rectal prolapse	CCO:MP0000493
MGI:88039	Apc	"Apc<Min>/Apc<+>,Blm<tm1Grdn>/Blm<+>"	involves: 129P2/OlaHsd * 129S/SvEv * Black Swiss * C57BL/6J	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:88039	Apc	Apc<tm1Cip>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:88039	Apc	Apc<tm1Cip>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:88039	Apc	Apc<tm1Cip>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:88039	Apc	Apc<tm1Cip>/Apc<tm1Cip>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:88039	Apc	"Apc<Min>/Apc<+>,Ereg<tm1Dwt>/Ereg<tm1Dwt>"	involves: 129S6/SvEvTac * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88039	Apc	Apc<tm3Mmt>/Apc<tm3Mmt>	involves: 129X1/SvJ * C57BL/6N	MP:0006108	abnormal hindbrain development	CCO:MP0006108
MGI:88039	Apc	Apc<tm1Cip>/Apc<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88059	App	App<tm2Umu>/App<tm2Umu>	involves: 129P2/OlaHsd * C57BL/6	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0002572	abnormal emotion/affect behavior	CCO:MP0002572
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0003313	abnormal locomotor activation	CCO:MP0003313
MGI:88059	App	"App<tm1Ck>/App<tm1Ck>,Tg(PDGFB-PSEN1M146L)2Jhd/0"	involves: 129 * Black Swiss * C57BL/6 * DBA/2 * SW	MP:0003329	amyloid beta deposits	CCO:MP0003329
MGI:88059	App	"App<tm1Ck>/App<tm1Ck>,Tg(PDGFB-PSEN1M146L)2Jhd/0"	involves: 129 * Black Swiss * C57BL/6 * DBA/2 * SW	MP:0001038	abnormal cholinergic neuron morphology	CCO:MP0001038
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0002797	increased thigmotaxis	CCO:MP0002797
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0001502	abnormal circadian rhythm	CCO:MP0001502
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0001515	abnormal grip strength	CCO:MP0001515
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0001417	decreased exploration in new environment	CCO:MP0001417
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0001522	impaired swimming	CCO:MP0001522
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas	MP:0002066	abnormal motor capabilities/coordination/movement	CCO:MP0002066
MGI:88059	App	App<tm1Somm>/App<tm1Somm>	C57BL/6-App<tm1Somm>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88059	App	App<tm1Sud>/App<tm1Sud>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:88059	App	"App<tm1Dbo>/App<+>,Dab1<tm1Bwh>/Dab1<tm1Bwh>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6	MP:0000852	small cerebellum	CCO:MP0000852
MGI:88059	App	App<tm1Somm>/App<tm1Somm>	C57BL/6-App<tm1Somm>	MP:0004000	impaired passive avoidance behavior	CCO:MP0004000
MGI:88059	App	App<tm1Somm>/App<tm1Somm>	C57BL/6-App<tm1Somm>	MP:0001515	abnormal grip strength	CCO:MP0001515
MGI:88059	App	"App<tm1Dbo>/App<tm1Dbo>,Dab1<tm1Bwh>/Dab1<tm1Bwh>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6	MP:0000852	small cerebellum	CCO:MP0000852
MGI:88059	App	App<tm1Somm>/App<tm1Somm>	C57BL/6-App<tm1Somm>	MP:0001402	hypoactivity	CCO:MP0001402
MGI:88059	App	App<tm1.1Cep>/App<tm1.1Cep>	involves: 129S1/Sv * 129X1/SvJ	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * 129S/SvEv	MP:0002196	absent corpus callosum	CCO:MP0002196
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * 129S/SvEv	MP:0002199	abnormal brain commissure morphology	CCO:MP0002199
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * 129S/SvEv	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm2Cwe>/App<tm2Cwe>"	involves: 129/Sv * 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0009546	absent gastric milk in neonates	CCO:MP0009546
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003717	pallor	CCO:MP0003717
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005191	head tilt	CCO:MP0005191
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001411	spinning	CCO:MP0001411
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001921	reduced fertility	CCO:MP0001921
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001523	impaired righting response	CCO:MP0001523
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001393	ataxia	CCO:MP0001393
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000746	weakness	CCO:MP0000746
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * 129S/SvEv	MP:0008222	decreased hippocampal commissure size	CCO:MP0008222
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:88059	App	App<tm1.1Cep>/App<+>	involves: 129S1/Sv * 129X1/SvJ	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:88059	App	App<tm1Cep>/App<tm1Cep>	involves: 129S1/Sv * 129X1/SvJ	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:88059	App	"Aplp1<tm1Umu>/Aplp1<tm1Umu>,App<tm2Cwe>/App<tm2Cwe>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001515	abnormal grip strength	CCO:MP0001515
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001402	hypoactivity	CCO:MP0001402
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002207	abnormal long term potentiation	CCO:MP0002207
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002183	gliosis	CCO:MP0002183
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002798	abnormal active avoidance behavior	CCO:MP0002798
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002882	abnormal neuron morphology	CCO:MP0002882
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003313	abnormal locomotor activation	CCO:MP0003313
MGI:88059	App	App<tm1Dbo>/App<tm1Dbo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003354	astrocytosis	CCO:MP0003354
MGI:88059	App	"Aplp2<tm1Dbo>/Aplp2<tm1Dbo>,App<tm1Dbo>/App<tm1Dbo>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	129S-App<tm1Cwe>	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * 129S/SvEv	MP:0008226	decreased anterior commissure size	CCO:MP0008226
MGI:88059	App	App<tm1Cep>/App<+>	involves: 129S1/Sv * 129X1/SvJ	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	129S-App<tm1Cwe>	MP:0008222	decreased hippocampal commissure size	CCO:MP0008222
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	129S-App<tm1Cwe>	MP:0002196	absent corpus callosum	CCO:MP0002196
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	129S-App<tm1Cwe>	MP:0002199	abnormal brain commissure morphology	CCO:MP0002199
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	129S-App<tm1Cwe>	MP:0008226	decreased anterior commissure size	CCO:MP0008226
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0008414	abnormal spatial reference memory	CCO:MP0008414
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0008226	decreased anterior commissure size	CCO:MP0008226
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0008222	decreased hippocampal commissure size	CCO:MP0008222
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0001454	abnormal cued conditioning behavior	CCO:MP0001454
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0002196	absent corpus callosum	CCO:MP0002196
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0002199	abnormal brain commissure morphology	CCO:MP0002199
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0001417	decreased exploration in new environment	CCO:MP0001417
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0002063	abnormal learning/memory/conditioning	CCO:MP0002063
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0002797	increased thigmotaxis	CCO:MP0002797
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	involves: 129S2/SvPas * C57BL/6	MP:0002065	abnormal fear/anxiety-related behavior	CCO:MP0002065
MGI:88059	App	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	MP:0002083	premature death	CCO:MP0002083
MGI:88059	App	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	MP:0002801	abnormal long term object recognition memory	CCO:MP0002801
MGI:88059	App	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	MP:0000787	abnormal telencephalon morphology	CCO:MP0000787
MGI:88059	App	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	MP:0001399	hyperactivity	CCO:MP0001399
MGI:88059	App	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88059	App	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	MP:0001449	abnormal learning/ memory	CCO:MP0001449
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * C57BL/6	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * C57BL/6	MP:0002199	abnormal brain commissure morphology	CCO:MP0002199
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * C57BL/6	MP:0000781	decreased corpus callosum size	CCO:MP0000781
MGI:88059	App	"App<tm1.1Cep>/App<tm1.1Cep>,Psen1<tm1Dgf>/Psen1<tm1Dgf>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0003329	amyloid beta deposits	CCO:MP0003329
MGI:88059	App	App<tm2Cwe>/App<tm2Cwe>	involves: 129P2/OlaHsd * C57BL/6	MP:0008222	decreased hippocampal commissure size	CCO:MP0008222
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	B6.129S2-App<tm1Cwe>	MP:0008226	decreased anterior commissure size	CCO:MP0008226
MGI:88059	App	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	MP:0003329	amyloid beta deposits	CCO:MP0003329
MGI:88059	App	App<tm1Ini>/App<+>	involves: C57BL/6 * CBA * CD-1	MP:0001392	abnormal locomotor activity	CCO:MP0001392
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	B6.129S2-App<tm1Cwe>	MP:0000781	decreased corpus callosum size	CCO:MP0000781
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	B6.129S2-App<tm1Cwe>	MP:0002199	abnormal brain commissure morphology	CCO:MP0002199
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	B6.129S2-App<tm1Cwe>	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:88059	App	App<tm1Cwe>/App<tm1Cwe>	B6.129S2-App<tm1Cwe>	MP:0008222	decreased hippocampal commissure size	CCO:MP0008222
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0003068	enlarged kidney	CCO:MP0003068
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0008585	absent photoreceptor outer segment	CCO:MP0008585
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0009343	dilated gall bladder	CCO:MP0009343
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0008518	retinal outer nuclear layer degeneration	CCO:MP0008518
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0004247	small pancreas	CCO:MP0004247
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0003254	bile duct inflammation	CCO:MP0003254
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0002928	abnormal bile duct morphology	CCO:MP0002928
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0001944	abnormal pancreas morphology	CCO:MP0001944
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0000527	abnormal kidney development	CCO:MP0000527
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0001265	decreased body size	CCO:MP0001265
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0001270	distended abdomen	CCO:MP0001270
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0009498	abnormal extrahepatic bile duct morphology	CCO:MP0009498
MGI:1929699	Arl3	Arl3<Gt(OST263303)Lex>/Arl3<Gt(OST263303)Lex>	involves: 129S5/SvEvBrd	MP:0002929	abnormal bile duct development	CCO:MP0002929
MGI:107202	Atm	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<+>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:107202	Atm	Atm<tm1Mfl>/Atm<+>	involves: 129T2/SvEms * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:107202	Atm	Atm<tm1Mfl>/Atm<+>	involves: 129T2/SvEms * C57BL/6J	MP:0002026	leukemia	CCO:MP0002026
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129 * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129 * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:107202	Atm	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0001265	decreased body size	CCO:MP0001265
MGI:107202	Atm	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:107202	Atm	"Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>,Atm<tm1Pmc>/Atm<tm1Pmc>"	involves: 129S1/Sv	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:107202	Atm	Atm<tm1Mfl>/Atm<+>	involves: 129T2/SvEms * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:107202	Atm	"Atm<tm1Pmc>/Atm<+>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:107202	Atm	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:107202	Atm	Atm<tm1Mfl>/Atm<+>	involves: 129T2/SvEms * C57BL/6J	MP:0002815	adenoma	CCO:MP0002815
MGI:107202	Atm	Atm<tm1Mfl>/Atm<+>	involves: 129T2/SvEms * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:107202	Atm	Atm<tm1Mfl>/Atm<+>	involves: 129T2/SvEms * C57BL/6J	MP:0008000	ovary tumor	CCO:MP0008000
MGI:107202	Atm	"Atm<tm1Led>/Atm<+>,Myst1<tm2Thl>/Myst1<+>"	involves: 129S1/Sv * 129S6/SvEvTac	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	"Atm<tm1Led>/Atm<tm1Led>,Myst1<tm2Thl>/Myst1<+>"	involves: 129S1/Sv * 129S6/SvEvTac	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	"Atm<tm1Led>/Atm<tm1Led>,Myst1<tm2Thl>/Myst1<+>"	involves: 129S1/Sv * 129S6/SvEvTac	MP:0001262	decreased body weight	CCO:MP0001262
MGI:107202	Atm	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	involves: 129	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>"	involves: 129S6/SvEvTac * 129/Sv	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:107202	Atm	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	involves: 129	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:107202	Atm	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Pmc>/Lig4<tm1Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * C57BL/6 * SJL	MP:0001393	ataxia	CCO:MP0001393
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001265	decreased body size	CCO:MP0001265
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0008082	increased single-positive T cell number	CCO:MP0008082
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0003830	abnormal testis development	CCO:MP0003830
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001658	increased mortality induced by gamma-irradiation	CCO:MP0001658
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001402	hypoactivity	CCO:MP0001402
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001405	impaired coordination	CCO:MP0001405
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001127	small ovary	CCO:MP0001127
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001147	small testis	CCO:MP0001147
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001407	short stride length	CCO:MP0001407
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001120	abnormal uterus morphology	CCO:MP0001120
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0001931	abnormal oogenesis	CCO:MP0001931
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0000716	abnormal immune system cell morphology	CCO:MP0000716
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0005159	azoospermia	CCO:MP0005159
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0005091	increased double-positive T cell number	CCO:MP0005091
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:107202	Atm	Atm<tm1Pmc>/Atm<tm1Pmc>	involves: 129X1/SvJ * C57BL/6	MP:0001924	infertility	CCO:MP0001924
MGI:107202	Atm	Atm<tm1Pmc>/Atm<tm1Pmc>	involves: 129X1/SvJ * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:107202	Atm	Atm<tm1Pmc>/Atm<tm1Pmc>	involves: 129X1/SvJ * C57BL/6	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0002217	small lymph nodes	CCO:MP0002217
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001919	abnormal reproductive system physiology	CCO:MP0001919
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0001402	hypoactivity	CCO:MP0001402
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0000885	ectopic Purkinje cell	CCO:MP0000885
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0008498	decreased IgG3 level	CCO:MP0008498
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0008497	decreased IgG2b level	CCO:MP0008497
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0008496	decreased IgG2a level	CCO:MP0008496
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0000706	small thymus	CCO:MP0000706
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0000692	small spleen	CCO:MP0000692
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0009339	decreased splenocyte number	CCO:MP0009339
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0005045	decreased thymus cortex area	CCO:MP0005045
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0000706	small thymus	CCO:MP0000706
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001925	male infertility	CCO:MP0001925
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001147	small testis	CCO:MP0001147
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001265	decreased body size	CCO:MP0001265
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0008572	abnormal Purkinje cell dendrite morphology	CCO:MP0008572
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0008215	decreased immature B cell number	CCO:MP0008215
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0002804	abnormal motor learning	CCO:MP0002804
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:107202	Atm	Atm<tm1Fwa>/Atm<tm1Fwa>	involves: 129S4/SvJae * C57BL/6	MP:0000890	thin cerebellar molecular layer	CCO:MP0000890
MGI:107202	Atm	Atm<tm1Mfl>/Atm<tm1Mfl>	involves: 129T2/SvEms * C57BL/6J	MP:0002722	abnormal immune system organ morphology	CCO:MP0002722
MGI:107202	Atm	Atm<tm1Led>/Atm<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0004805	absent oocytes	CCO:MP0004805
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0009021	absent estrus	CCO:MP0009021
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0004805	absent oocytes	CCO:MP0004805
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0003674	oxidative stress	CCO:MP0003674
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0005091	increased double-positive T cell number	CCO:MP0005091
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0002757	decreased vertical activity	CCO:MP0002757
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0005058	abnormal lysosome morphology	CCO:MP0005058
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001830	decreased activated T cell number	CCO:MP0001830
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001925	male infertility	CCO:MP0001925
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001926	female infertility	CCO:MP0001926
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	either: 129S6/SvEvTac-Atm<tm1Awb> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0005159	azoospermia	CCO:MP0005159
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0003224	neuron degeneration	CCO:MP0003224
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0004098	abnormal granule neuron	CCO:MP0004098
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0000876	Purkinje cell degeneration	CCO:MP0000876
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0001805	decreased IgG level	CCO:MP0001805
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0000706	small thymus	CCO:MP0000706
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0001925	male infertility	CCO:MP0001925
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0000889	abnormal cerebellar molecular layer	CCO:MP0000889
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0001926	female infertility	CCO:MP0001926
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0002444	abnormal T cell physiology	CCO:MP0002444
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0001262	decreased body weight	CCO:MP0001262
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0003691	abnormal microglial cell physiology	CCO:MP0003691
MGI:107202	Atm	Atm<tm1Bal>/Atm<tm1Bal>	involves: 129S4/SvJae	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:107202	Atm	"Atm<tm1Awb>/Atm<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:107202	Atm	"Atm<tm1Awb>/Atm<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	"Atm<tm1Awb>/Atm<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	involves: 129S6/SvEvTac * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	involves: 129S6/SvEvTac * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:107202	Atm	"Atm<tm1Awb>/Atm<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:107202	Atm	Atm<tm1Pmc>/Atm<tm1Pmc>	Not Specified	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:107202	Atm	Atm<tm1Pmc>/Atm<tm1Pmc>	Not Specified	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:107202	Atm	"Atm<tm1Awb>/Atm<tm1Awb>,Nbn<tm1Jpt>/Nbn<tm1Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	involves: 129S6/SvEvTac * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:107202	Atm	Atm<tm1Awb>/Atm<tm1Awb>	involves: 129S6/SvEvTac * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0001200	thick skin	CCO:MP0001200
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002703	abnormal renal tubule morphology	CCO:MP0002703
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0001859	kidney inflammation	CCO:MP0001859
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0008844	decreased subcutaneous adipose tissue amount	CCO:MP0008844
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000427	abnormal hair cycle	CCO:MP0000427
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0003809	abnormal hair shaft morphology	CCO:MP0003809
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000414	alopecia	CCO:MP0000414
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0003704	abnormal hair follicle development	CCO:MP0003704
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0003141	cardiac fibrosis	CCO:MP0003141
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000160	kyphosis	CCO:MP0000160
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000066	osteoporosis	CCO:MP0000066
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000379	decreased hair follicle number	CCO:MP0000379
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000488	abnormal intestinal epithelium morphology	CCO:MP0000488
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000423	delayed hair regrowth	CCO:MP0000423
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0003985	renal fibrosis	CCO:MP0003985
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000135	decreased cortical bone thickness	CCO:MP0000135
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000130	abnormal cancellous bone morphology	CCO:MP0000130
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000647	abnormal sebaceous gland morphology	CCO:MP0000647
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000377	abnormal hair follicle morphology	CCO:MP0000377
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002075	abnormal coat/hair pigmentation	CCO:MP0002075
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002073	abnormal hair growth	CCO:MP0002073
MGI:108028	Atr	"Atr<tm1Bal>/Atr<tm2Bal>,Tg(UBC-cre/ESR1)1Ejb/0"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0001824	abnormal thymus involution	CCO:MP0001824
MGI:108028	Atr	Atr<tm1Bal>/Atr<tm1Bal>	involves: 129 * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:108028	Atr	Atr<tm1Bal>/Atr<+>	involves: 129 * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:108028	Atr	Atr<tm1Bal>/Atr<+>	involves: 129 * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:108028	Atr	Atr<tm1Akl>/Atr<tm1Akl>	involves: 129P2/OlaHsd * C57BL/6	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:894678	Aurka	Aurka<tm1.2Tvd>/Aurka<tm1.2Tvd>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<+>	involves: 129P2/OlaHsd	MP:0002022	lymphoma	CCO:MP0002022
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<+>	involves: 129P2/OlaHsd	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<+>	involves: 129P2/OlaHsd	MP:0008714	lung carcinoma	CCO:MP0008714
MGI:894678	Aurka	"Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<+>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0004760	increased mitotic index	CCO:MP0004760
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<+>	involves: 129P2/OlaHsd	MP:0004024	aneuploidy	CCO:MP0004024
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<+>	involves: 129P2/OlaHsd	MP:0002028	hepatoma	CCO:MP0002028
MGI:894678	Aurka	Aurka<tm1.2Tvd>/Aurka<tm1.2Tvd>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004760	increased mitotic index	CCO:MP0004760
MGI:894678	Aurka	Aurka<tm1.2Tvd>/Aurka<tm1.2Tvd>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:894678	Aurka	Aurka<tm1.2Tvd>/Aurka<tm1.2Tvd>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:894678	Aurka	Aurka<tm1.2Tvd>/Aurka<tm1.2Tvd>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000329	decreased cell number	CCO:MP0000329
MGI:894678	Aurka	"Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<+>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:894678	Aurka	"Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<+>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:894678	Aurka	"Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<tm1Sor>"	involves: 129 * 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	MP:0004760	increased mitotic index	CCO:MP0004760
MGI:894678	Aurka	"Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<tm1Sor>"	involves: 129 * 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:894678	Aurka	"Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<tm1Sor>"	involves: 129 * 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:894678	Aurka	"Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<tm1Sor>"	involves: 129 * 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<+>	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<Gt(XQ0149)Wtsi>	involves: 129P2/OlaHsd	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<Gt(XQ0149)Wtsi>	involves: 129P2/OlaHsd	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<Gt(XQ0149)Wtsi>	involves: 129P2/OlaHsd	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:894678	Aurka	Aurka<Gt(XQ0149)Wtsi>/Aurka<+>	involves: 129P2/OlaHsd	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:894678	Aurka	"Aurka<tm1.1Tvd>/Aurka<tm1.1Tvd>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<tm1Sor>"	involves: 129 * 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1321119	Aurkc	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	MP:0009231	detached acrosome	CCO:MP0009231
MGI:1321119	Aurkc	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	MP:0001935	decreased litter size	CCO:MP0001935
MGI:1321119	Aurkc	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	MP:0008898	abnormal acrosome morphology	CCO:MP0008898
MGI:1321119	Aurkc	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	MP:0009230	abnormal sperm head morphology	CCO:MP0009230
MGI:1321119	Aurkc	Aurkc<tm1Lex>/Aurkc<tm1Lex>	B6.129S-Aurkc<tm1Lex>	MP:0009232	abnormal sperm nucleus morphology	CCO:MP0009232
MGI:1097161	Bak1	"Hax1<tm1Jni>/Hax1<tm1Jni>,Bak1<tm1Thsn>/Bak1<tm1Thsn>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1097161	Bak1	Bak1<tm1Thsn>/Bak1<tm1Thsn>	B6.129-Bak1<tm1Thsn>	MP:0005464	abnormal platelet physiology	CCO:MP0005464
MGI:1097161	Bak1	Bak1<tm1Thsn>/Bak1<tm1Thsn>	B6.129-Bak1<tm1Thsn>	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<+>,Bcl2l1<tm1Dlo>/Bcl2l1<+>"	B6.Cg-Bcl2l1<tm1Dlo> Bak1<tm1Thsn>	MP:0004720	abnormal platelet morphology	CCO:MP0004720
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<+>,Bcl2l1<Plt20>/Bcl2l1<+>"	involves: 129 * BALB/c * C57BL/6	MP:0004720	abnormal platelet morphology	CCO:MP0004720
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bcl2l1<tm1Dlo>/Bcl2l1<+>"	B6.Cg-Bcl2l1<tm1Dlo> Bak1<tm1Thsn>	MP:0005464	abnormal platelet physiology	CCO:MP0005464
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bcl2l1<tm1Dlo>/Bcl2l1<+>"	B6.Cg-Bcl2l1<tm1Dlo> Bak1<tm1Thsn>	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0001394	circling	CCO:MP0001394
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0009333	abnormal splenocyte physiology	CCO:MP0009333
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0001963	abnormal hearing physiology	CCO:MP0001963
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0001144	vagina atresia	CCO:MP0001144
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0005013	increased lymphocyte cell number	CCO:MP0005013
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008037	abnormal T cell morphology	CCO:MP0008037
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008947	increased neuron number	CCO:MP0008947
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008478	increased spleen white pulp amount	CCO:MP0008478
MGI:1097161	Bak1	Bak1<tm1Thsn>/Bak1<tm1Thsn>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008476	increased spleen red pulp amount	CCO:MP0008476
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0005238	increased brain size	CCO:MP0005238
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0004939	abnormal B cell morphology	CCO:MP0004939
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0002064	seizures	CCO:MP0002064
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002494	increased IgM level	CCO:MP0002494
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008206	increased B-2 B cell number	CCO:MP0008206
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008189	increased transitional stage B cell number	CCO:MP0008189
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008186	increased pro-B cell number	CCO:MP0008186
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008182	decreased marginal zone B cell number	CCO:MP0008182
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008173	increased follicular B cell number	CCO:MP0008173
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0005014	increased B cell number	CCO:MP0005014
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002493	increased IgG level	CCO:MP0002493
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002495	increased IgA level	CCO:MP0002495
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002458	abnormal B cell number	CCO:MP0002458
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002461	increased immunoglobulin level	CCO:MP0002461
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002459	abnormal B cell physiology	CCO:MP0002459
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0003132	increased pre-B cell number	CCO:MP0003132
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005014	increased B cell number	CCO:MP0005014
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005013	increased lymphocyte cell number	CCO:MP0005013
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002993	arthritis	CCO:MP0002993
MGI:1097161	Bak1	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005350	increased susceptibility to autoimmune disorder	CCO:MP0005350
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ * C57BL/6	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Ntf3<tm1Jae>/Ntf3<tm1Jae>"	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	MP:0008468	absent muscle spindles	CCO:MP0008468
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Ntf3<tm1Jae>/Ntf3<tm1Jae>"	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	MP:0004297	abnormal proprioceptive neuron morphology	CCO:MP0004297
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Kitl<Sl>/Kitl<Sl>,Tg(Pou5f1-GFP)1Scho/?"	involves: 129X1/SvJ * C3H * CD1 * FVB	MP:0001919	abnormal reproductive system physiology	CCO:MP0001919
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Kitl<Sl>/Kitl<Sl>,Tg(Pou5f1-GFP)1Scho/?"	involves: 129X1/SvJ * C3H * CD1 * FVB	MP:0002982	abnormal primordial germ cell migration	CCO:MP0002982
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<+>,Kitl<Sl>/Kitl<Sl>,Tg(Pou5f1-GFP)1Scho/?"	involves: 129X1/SvJ * C3H * CD1 * FVB	MP:0008390	abnormal primordial germ cell proliferation	CCO:MP0008390
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Ntf3<tm1Jae>/Ntf3<tm1Jae>"	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0003651	abnormal axon outgrowth	CCO:MP0003651
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0006006	increased sensory neuron number	CCO:MP0006006
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<+>,Nanos2<tm1Ysa>/Nanos2<tm1Ysa>"	involves: 129S1/Sv * 129X1/SvJ	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:99702	Bax	Bax<tm1Sjk>/Bax<+>	involves: 129X1/SvJ	MP:0001025	abnormal sympathetic neuron morphology	CCO:MP0001025
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Lama2<tm1Eeng>/Lama2<tm1Eeng>"	B6.129-Bax<tm1Sjk> Lama2<tm1Eeng>	MP:0001661	extended life span	CCO:MP0001661
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Hax1<tm1Jni>/Hax1<tm1Jni>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<+>,Nanos2<tm1Ysa>/Nanos2<tm1Ysa>"	involves: 129S1/Sv * 129X1/SvJ	MP:0005159	azoospermia	CCO:MP0005159
MGI:99702	Bax	Bax<tm1Sjk>/Bax<+>	involves: 129X1/SvJ	MP:0005192	increased motor neuron number	CCO:MP0005192
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Nanos2<tm1Ysa>/Nanos2<tm1Ysa>"	involves: 129S1/Sv * 129X1/SvJ	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Nanos2<tm1Ysa>/Nanos2<tm1Ysa>"	involves: 129S1/Sv * 129X1/SvJ	MP:0005159	azoospermia	CCO:MP0005159
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Lama2<tm1Eeng>/Lama2<tm1Eeng>"	B6.129-Bax<tm1Sjk> Lama2<tm1Eeng>	MP:0001265	decreased body size	CCO:MP0001265
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Lama2<tm1Eeng>/Lama2<tm1Eeng>"	B6.129-Bax<tm1Sjk> Lama2<tm1Eeng>	MP:0002089	abnormal postnatal growth/weight/body size	CCO:MP0002089
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Lama2<tm1Eeng>/Lama2<tm1Eeng>"	B6.129-Bax<tm1Sjk> Lama2<tm1Eeng>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Lama2<tm1Eeng>/Lama2<tm1Eeng>"	B6.129-Bax<tm1Sjk> Lama2<tm1Eeng>	MP:0003084	abnormal skeletal muscle fiber morphology	CCO:MP0003084
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Lama2<tm1Eeng>/Lama2<tm1Eeng>"	B6.129-Bax<tm1Sjk> Lama2<tm1Eeng>	MP:0004818	increased skeletal muscle mass	CCO:MP0004818
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bmpr1a<tm1Bhr>/Bmpr1a<tm2.1Bhr>,Tg(Sftpc-cre)1Blh/0"	involves: 129 * C57BL/6 * DBA/2 * ICR	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Lama2<tm1Eeng>/Lama2<tm1Eeng>"	B6.129-Bax<tm1Sjk> Lama2<tm1Eeng>	MP:0000750	abnormal muscle regeneration	CCO:MP0000750
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0002064	seizures	CCO:MP0002064
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>"	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: C57BL/6	MP:0009083	uterus hypertrophy	CCO:MP0009083
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: C57BL/6	MP:0008870	increased mature ovarian follicle number	CCO:MP0008870
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: C57BL/6	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0004939	abnormal B cell morphology	CCO:MP0004939
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>"	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008476	increased spleen red pulp amount	CCO:MP0008476
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008478	increased spleen white pulp amount	CCO:MP0008478
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008947	increased neuron number	CCO:MP0008947
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0005192	increased motor neuron number	CCO:MP0005192
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0001925	male infertility	CCO:MP0001925
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0000714	increased thymocyte number	CCO:MP0000714
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>"	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>"	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<+>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>"	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<+>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>"	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<+>,Bcl2l1<tm1Mam>/Bcl2l1<tm1Mam>"	involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0009333	abnormal splenocyte physiology	CCO:MP0009333
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0005159	azoospermia	CCO:MP0005159
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0005014	increased B cell number	CCO:MP0005014
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0001011	abnormal superior cervical ganglion morphology	CCO:MP0001011
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0000909	abnormal facial motor nucleus morphology	CCO:MP0000909
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0008037	abnormal T cell morphology	CCO:MP0008037
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0001394	circling	CCO:MP0001394
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0001025	abnormal sympathetic neuron morphology	CCO:MP0001025
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0001144	vagina atresia	CCO:MP0001144
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0005013	increased lymphocyte cell number	CCO:MP0005013
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0005238	increased brain size	CCO:MP0005238
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	involves: 129X1/SvJ	MP:0001078	abnormal phrenic nerve morphology	CCO:MP0001078
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm1Sjk>"	involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6	MP:0001963	abnormal hearing physiology	CCO:MP0001963
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008186	increased pro-B cell number	CCO:MP0008186
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Ntrk1<tm2(Ntrk3)Apat>/Ntrk1<tm2(Ntrk3)Apat>"	involves: 129S1/SvImJ	MP:0004297	abnormal proprioceptive neuron morphology	CCO:MP0004297
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002993	arthritis	CCO:MP0002993
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Gdnf<tm1Rosl>/Gdnf<+>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0001046	abnormal enteric neuron morphology	CCO:MP0001046
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002493	increased IgG level	CCO:MP0002493
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002495	increased IgA level	CCO:MP0002495
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008182	decreased marginal zone B cell number	CCO:MP0008182
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002458	abnormal B cell number	CCO:MP0002458
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002494	increased IgM level	CCO:MP0002494
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005013	increased lymphocyte cell number	CCO:MP0005013
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008173	increased follicular B cell number	CCO:MP0008173
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005014	increased B cell number	CCO:MP0005014
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0003132	increased pre-B cell number	CCO:MP0003132
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0005014	increased B cell number	CCO:MP0005014
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	MP:0005159	azoospermia	CCO:MP0005159
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008206	increased B-2 B cell number	CCO:MP0008206
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0008189	increased transitional stage B cell number	CCO:MP0008189
MGI:99702	Bax	Bax<tm1Dlo>/Bax<tm1Dlo>	involves: 129P2/OlaHsd	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:99702	Bax	Bax<tm1Ofxa>/Bax<tm1Ofxa>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:99702	Bax	Bax<tm1Dlo>/Bax<tm1Dlo>	involves: 129P2/OlaHsd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002459	abnormal B cell physiology	CCO:MP0002459
MGI:99702	Bax	"Bax<tm1Dlo>/Bax<tm1Dlo>,Bcl2l1<tm1Dlo>/Bcl2l1<tm1Dlo>"	involves: 129P2/OlaHsd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:99702	Bax	"Bax<tm1Dlo>/Bax<tm1Dlo>,Bcl2l1<tm1Dlo>/Bcl2l1<tm1Dlo>"	involves: 129P2/OlaHsd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005350	increased susceptibility to autoimmune disorder	CCO:MP0005350
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	MP:0006304	abnormal seminiferous epithelium morphology	CCO:MP0006304
MGI:99702	Bax	"Bak1<tm1Thsn>/Bak1<tm1Thsn>,Bax<tm1Sjk>/Bax<tm2Sjk>,Cd19<tm1(cre)Cgn>/Cd19<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0002461	increased immunoglobulin level	CCO:MP0002461
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	MP:0001925	male infertility	CCO:MP0001925
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	MP:0005159	azoospermia	CCO:MP0005159
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	MP:0001925	male infertility	CCO:MP0001925
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:99702	Bax	Bax<tm1Sjk>/Bax<tm1Sjk>	B6.129X1-Bax<tm1Sjk>/J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Ntrk1<tm2(Ntrk3)Apat>/Ntrk1<tm2(Ntrk3)Apat>"	involves: 129S1/SvImJ	MP:0008485	increased muscle spindle number	CCO:MP0008485
MGI:99702	Bax	"Bax<tm1Sjk>/Bax<tm1Sjk>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2l11<tm1.1Ast> Bax<tm1Sjk>	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:88138	Bcl2	Bcl2<tm1Lbox>/Bcl2<tm1Lbox>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0005093	decreased B cell proliferation	CCO:MP0005093
MGI:88138	Bcl2	"Bcl2<tm1Mpin>/Bcl2<tm1Mpin>,Tg(SFTPC-RAF1-BxB)1Urr/0"	involves: 129S2/SvPas * C57BL/6 * DBA/2	MP:0002048	lung adenoma	CCO:MP0002048
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0000018	small ears	CCO:MP0000018
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0000692	small spleen	CCO:MP0000692
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0002444	abnormal T cell physiology	CCO:MP0002444
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0000706	small thymus	CCO:MP0000706
MGI:88138	Bcl2	"Bcl2<tm1Mpin>/Bcl2<tm1Mpin>,Tg(SFTPC-RAF1-BxB)1Urr/0"	involves: 129S2/SvPas * C57BL/6 * DBA/2	MP:0005514	increased resistance to tumor development	CCO:MP0005514
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0000394	absent hair follicle melanin granules	CCO:MP0000394
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0002619	abnormal lymphocyte morphology	CCO:MP0002619
MGI:88138	Bcl2	Bcl2<tm1Lbox>/Bcl2<tm1Lbox>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0005408	hypopigmentation	CCO:MP0005408
MGI:88138	Bcl2	Bcl2<tm1Lbox>/Bcl2<tm1Lbox>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:88138	Bcl2	Bcl2<tm1Lbox>/Bcl2<tm1Lbox>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0008211	decreased mature B cell number	CCO:MP0008211
MGI:88138	Bcl2	Bcl2<tm1Lbox>/Bcl2<tm1Lbox>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0008215	decreased immature B cell number	CCO:MP0008215
MGI:88138	Bcl2	Bcl2<tm1Lbox>/Bcl2<tm1Lbox>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0008217	abnormal B cell activation	CCO:MP0008217
MGI:88138	Bcl2	Bcl2<tm1Lbox>/Bcl2<tm1Lbox>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0008782	increased B cell apoptosis	CCO:MP0008782
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0001265	decreased body size	CCO:MP0001265
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88138	Bcl2	Bcl2<tm1Lbox>/Bcl2<tm1Lbox>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0002144	abnormal B cell differentiation	CCO:MP0002144
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0002083	premature death	CCO:MP0002083
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	B6;129S2-Bcl2<tm1Sjk>/J	MP:0009409	abnormal skeletal muscle fiber type ratio	CCO:MP0009409
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0009051	dilated distal convoluted tubules	CCO:MP0009051
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0009050	dilated proximal convoluted tubules	CCO:MP0009050
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology	CCO:MP0004841
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0004505	decreased renal glomerulus number	CCO:MP0004505
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0003644	thymus atrophy	CCO:MP0003644
MGI:88138	Bcl2	Bcl2<tm1Tsu>/Bcl2<tm1Tsu>	involves: 129P2/OlaHsd * ICR	MP:0003643	spleen atrophy	CCO:MP0003643
MGI:88138	Bcl2	"Bcl2<tm1Irt>/Bcl2<tm1Irt>,Lyz2<tm1(cre)Ifo>/Lyz2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002451	abnormal macrophage physiology	CCO:MP0002451
MGI:88138	Bcl2	"Apoe<tm1Bres>/Apoe<tm1Bres>,Bcl2<tm1Irt>/Bcl2<tm1Irt>,Lyz2<tm1(cre)Ifo>/Lyz2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002451	abnormal macrophage physiology	CCO:MP0002451
MGI:88138	Bcl2	"Apoe<tm1Bres>/Apoe<tm1Bres>,Bcl2<tm1Irt>/Bcl2<tm1Irt>,Lyz2<tm1(cre)Ifo>/Lyz2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0005338	atherosclerotic lesions	CCO:MP0005338
MGI:88138	Bcl2	Bcl2<drn>/Bcl2<drn>	either: C57BL/6JApb-Bcl2<drn> or (involves: C57BL/6JApb * CBA)	MP:0000372	irregular coat pigmentation	CCO:MP0000372
MGI:88138	Bcl2	Bcl2<drn>/Bcl2<drn>	either: C57BL/6JApb-Bcl2<drn> or (involves: C57BL/6JApb * CBA)	MP:0000371	diluted coat color	CCO:MP0000371
MGI:88138	Bcl2	"Bcl2<tm1Mpin>/Bcl2<tm1Mpin>,Tg(H2-K-BCL2)1Josd/0,Tg(SFTPC-RAF1-BxB)1Urr/0"	involves: 129S2/SvPas * C3H * C57BL/6 * DBA/2	MP:0002048	lung adenoma	CCO:MP0002048
MGI:88138	Bcl2	"Bcl2<tm1Mpin>/Bcl2<+>,Tg(SFTPC-RAF1-BxB)1Urr/0"	involves: 129S2/SvPas * C57BL/6 * DBA/2	MP:0002048	lung adenoma	CCO:MP0002048
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<+>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0000371	diluted coat color	CCO:MP0000371
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0000018	small ears	CCO:MP0000018
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0000692	small spleen	CCO:MP0000692
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002356	abnormal spleen red pulp morphology	CCO:MP0002356
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002357	abnormal spleen white pulp morphology	CCO:MP0002357
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0000706	small thymus	CCO:MP0000706
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002432	abnormal CD4-positive T cell morphology	CCO:MP0002432
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005010	abnormal CD8-positive T cell morphology	CCO:MP0005010
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002722	abnormal immune system organ morphology	CCO:MP0002722
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<+>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0003945	abnormal lymphocyte physiology	CCO:MP0003945
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005150	cachexia	CCO:MP0005150
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002828	abnormal renal glomerular capsule	CCO:MP0002828
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005408	hypopigmentation	CCO:MP0005408
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005553	increased circulating creatinine level	CCO:MP0005553
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002989	small kidney	CCO:MP0002989
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0003068	enlarged kidney	CCO:MP0003068
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0006057	decreased vascular endothelial cell number	CCO:MP0006057
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0003719	abnormal pericyte morphology	CCO:MP0003719
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0004805	absent oocytes	CCO:MP0004805
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002703	abnormal renal tubule morphology	CCO:MP0002703
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0003014	abnormal kidney medulla morphology	CCO:MP0003014
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0002075	abnormal coat/hair pigmentation	CCO:MP0002075
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0002233	abnormal nose morphology	CCO:MP0002233
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0000018	small ears	CCO:MP0000018
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0000521	abnormal kidney cortex	CCO:MP0000521
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0000703	abnormal thymus morphology	CCO:MP0000703
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0002989	small kidney	CCO:MP0002989
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0000445	short snout	CCO:MP0000445
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0004505	decreased renal glomerulus number	CCO:MP0004505
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0008211	decreased mature B cell number	CCO:MP0008211
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0000443	abnormal snout morphology	CCO:MP0000443
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0001824	abnormal thymus involution	CCO:MP0001824
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0002792	abnormal retinal vasculature	CCO:MP0002792
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	involves: 129P2/OlaHsd * C57BL/6	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0006413	increased T cell apoptosis	CCO:MP0006413
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<+>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0000394	absent hair follicle melanin granules	CCO:MP0000394
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<+>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0006413	increased T cell apoptosis	CCO:MP0006413
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0002083	premature death	CCO:MP0002083
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0000018	small ears	CCO:MP0000018
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0000527	abnormal kidney development	CCO:MP0000527
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0005460	abnormal leukopoiesis	CCO:MP0005460
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0003675	kidney cysts	CCO:MP0003675
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<+>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0002075	abnormal coat/hair pigmentation	CCO:MP0002075
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<+>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0004381	abnormal hair follicle melanocyte morphology	CCO:MP0004381
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0008782	increased B cell apoptosis	CCO:MP0008782
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0005460	abnormal leukopoiesis	CCO:MP0005460
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0008783	decreased B cell apoptosis	CCO:MP0008783
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0006413	increased T cell apoptosis	CCO:MP0006413
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0006413	increased T cell apoptosis	CCO:MP0006413
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bcl2l11<tm1.1Ast>/Bcl2l11<tm1.1Ast>"	B6.129-Bcl2<tm1Dlo> Bcl2l11<tm1.1Ast>	MP:0003945	abnormal lymphocyte physiology	CCO:MP0003945
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0003945	abnormal lymphocyte physiology	CCO:MP0003945
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0000938	motor neuron degeneration	CCO:MP0000938
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0009050	dilated proximal convoluted tubules	CCO:MP0009050
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0009051	dilated distal convoluted tubules	CCO:MP0009051
MGI:88138	Bcl2	Bcl2<tm1Sjk>/Bcl2<tm1Sjk>	involves: 129S2/SvPas * C57BL/6	MP:0009361	abnormal primordial ovarian follicle morphology	CCO:MP0009361
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88138	Bcl2	Bcl2<tm1Dlo>/Bcl2<tm1Dlo>	B6.129P2-Bcl2<tm1Dlo>	MP:0001265	decreased body size	CCO:MP0001265
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0001330	abnormal optic nerve morphology	CCO:MP0001330
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0001025	abnormal sympathetic neuron morphology	CCO:MP0001025
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0005553	increased circulating creatinine level	CCO:MP0005553
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0000909	abnormal facial motor nucleus morphology	CCO:MP0000909
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0000966	decreased sensory neuron number	CCO:MP0000966
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0001011	abnormal superior cervical ganglion morphology	CCO:MP0001011
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0008067	retinal ganglion cell degeneration	CCO:MP0008067
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:88138	Bcl2	Bcl2<tm1Mpin>/Bcl2<tm1Mpin>	involves: 129S2/SvPas * C57BL/6	MP:0006405	abnormal L3 dorsal root ganglion morphology	CCO:MP0006405
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bik<tm1Ast>/Bik<tm1Ast>"	B6.Cg-Bcl2<tm1Dlo> Bik<tm1Ast>	MP:0002083	premature death	CCO:MP0002083
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bik<tm1Ast>/Bik<tm1Ast>"	B6.Cg-Bcl2<tm1Dlo> Bik<tm1Ast>	MP:0003945	abnormal lymphocyte physiology	CCO:MP0003945
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bik<tm1Ast>/Bik<tm1Ast>"	B6.Cg-Bcl2<tm1Dlo> Bik<tm1Ast>	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:88138	Bcl2	"Bcl2<tm1Dlo>/Bcl2<tm1Dlo>,Bik<tm1Ast>/Bik<tm1Ast>"	B6.Cg-Bcl2<tm1Dlo> Bik<tm1Ast>	MP:0001265	decreased body size	CCO:MP0001265
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0002941	increased circulating alanine transaminase level	CCO:MP0002941
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0001263	weight loss	CCO:MP0001263
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0002463	abnormal neutrophil physiology	CCO:MP0002463
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0002581	abnormal ileum morphology	CCO:MP0002581
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0005343	increased circulating aspartate transaminase level	CCO:MP0005343
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0000219	increased neutrophil cell number	CCO:MP0000219
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0002944	increased lactate dehydrogenase level	CCO:MP0002944
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0003288	intestinal edema	CCO:MP0003288
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0003946	renal necrosis	CCO:MP0003946
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0004756	abnormal proximal convoluted tubule morphology	CCO:MP0004756
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0008735	increased susceptibility to endotoxin shock	CCO:MP0008735
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0008986	abnormal liver parenchyma morphology	CCO:MP0008986
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:88141	Bcr	Bcr<tm1Hkp>/Bcr<tm1Hkp>	involves: 129S2/SvPas	MP:0005044	sepsis	CCO:MP0005044
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0001525	impaired balance	CCO:MP0001525
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0001405	impaired coordination	CCO:MP0001405
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0001399	hyperactivity	CCO:MP0001399
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0002762	ectopic granule cells	CCO:MP0002762
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0008916	abnormal astrocyte physiology	CCO:MP0008916
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0003648	abnormal radial glial cell morphology	CCO:MP0003648
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0003938	abnormal ear development	CCO:MP0003938
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0006090	abnormal utricle morphology	CCO:MP0006090
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0001522	impaired swimming	CCO:MP0001522
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0001394	circling	CCO:MP0001394
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0000034	abnormal vestibule morphology	CCO:MP0000034
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0000952	abnormal CNS glial cell morphology	CCO:MP0000952
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0002182	abnormal astrocyte morphology	CCO:MP0002182
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0000849	abnormal cerebellum morphology	CCO:MP0000849
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0002978	absent otoliths	CCO:MP0002978
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0003143	enlarged otoliths	CCO:MP0003143
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0003144	decreased otolith number	CCO:MP0003144
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0002183	gliosis	CCO:MP0002183
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0006089	abnormal saccule morphology	CCO:MP0006089
MGI:88141	Bcr	"Abr<tm1Jhg>/Abr<tm1Jhg>,Bcr<tm1Hkp>/Bcr<tm1Hkp>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0001860	liver inflammation	CCO:MP0001860
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0001861	lung inflammation	CCO:MP0001861
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0001304	cataracts	CCO:MP0001304
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:1929883	Bin3	Bin3<tm1Gcp>/Bin3<tm1Gcp>	involves: 129 * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:1203517	Birc5	Birc5<tm1Emc>/Birc5<+>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0005165	increased susceptibility to injury	CCO:MP0005165
MGI:1203517	Birc5	Birc5<tm1Emc>/Birc5<+>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0002954	abnormal aerobic energy metabolism	CCO:MP0002954
MGI:1203517	Birc5	Birc5<tm1Emc>/Birc5<+>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:1203517	Birc5	"Birc5<tm1Wnt>/Birc5<tm1Emc>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:1203517	Birc5	Birc5<tm1Emc>/Birc5<tm1Emc>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1203517	Birc5	"Birc5<tm1Wnt>/Birc5<tm1Emc>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:1203517	Birc5	"Birc5<tm1Wnt>/Birc5<tm1Emc>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0002217	small lymph nodes	CCO:MP0002217
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1203517	Birc5	"Birc5<tm1Wnt>/Birc5<tm1Emc>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0003706	abnormal nucleus count	CCO:MP0003706
MGI:1203517	Birc5	"Birc5<tm1Wnt>/Birc5<tm1Emc>,Tg(CD4-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:1203517	Birc5	"Birc5<tm1Wnt>/Birc5<tm1Emc>,Tg(Lck-cre)1Cwi/?"	involves: C57BL/6 * DBA/2	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0001714	absent trophoblast giant cells	CCO:MP0001714
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0002663	failure to form blastocele	CCO:MP0002663
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0003708	binucleate	CCO:MP0003708
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0004965	inner cell mass degeneration	CCO:MP0004965
MGI:1203517	Birc5	Birc5<tm1Vaux>/Birc5<tm1Vaux>	C57BL/6-Birc5<tm1Vaux>	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1203517	Birc5	Birc5<tm1Mak>/Birc5<tm1Mak>	involves: 129P2/OlaHsd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1203517	Birc5	"Birc5<tm1Mak>/Birc5<tm1Mak>,Tg(Lck-cre)I57Jxm/0"	involves: 129P2/OlaHsd	MP:0009543	abnormal thymus corticomedullary boundary morphology	CCO:MP0009543
MGI:1203517	Birc5	"Birc5<tm1Mak>/Birc5<tm1Mak>,Tg(Lck-cre)I57Jxm/0"	involves: 129P2/OlaHsd	MP:0000706	small thymus	CCO:MP0000706
MGI:1203517	Birc5	"Birc5<tm1Mak>/Birc5<tm1Mak>,Tg(Lck-cre)I57Jxm/0"	involves: 129P2/OlaHsd	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1203517	Birc5	"Birc5<tm1Mak>/Birc5<tm1Mak>,Tg(Lck-cre)I57Jxm/0"	involves: 129P2/OlaHsd	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:1203517	Birc5	"Birc5<tm1Mak>/Birc5<tm1Mak>,Tg(Lck-cre)I57Jxm/0"	involves: 129P2/OlaHsd	MP:0008037	abnormal T cell morphology	CCO:MP0008037
MGI:1203517	Birc5	"Birc5<tm1Mak>/Birc5<tm1Mak>,Tg(Lck-cre)I57Jxm/0"	involves: 129P2/OlaHsd	MP:0006413	increased T cell apoptosis	CCO:MP0006413
MGI:1203517	Birc5	"Birc5<tm1Mak>/Birc5<tm1Mak>,Tg(Lck-cre)I57Jxm/0"	involves: 129P2/OlaHsd	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:104537	Brca1	"Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:104537	Brca1	"Brca1<tm1Aash>/Brca1<tm1Aash>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000621	salivary adenocarcinoma	CCO:MP0000621
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:104537	Brca1	"Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	MP:0009508	mammary gland ductal carcinoma	CCO:MP0009508
MGI:104537	Brca1	"Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000630	mammary gland hyperplasia	CCO:MP0000630
MGI:104537	Brca1	Brca1<tm1Brn>/Brca1<tm1Brn>	involves: 129P2/OlaHsd	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:104537	Brca1	"Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	MP:0000621	salivary adenocarcinoma	CCO:MP0000621
MGI:104537	Brca1	Brca1<tm1Aash>/Brca1<tm1Aash>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104537	Brca1	"Brca1<tm1Brn>/Brca1<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0009092	endometrium hyperplasia	CCO:MP0009092
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0009503	abnormal mammary gland duct morphology	CCO:MP0009503
MGI:104537	Brca1	Brca1<tm1Brn>/Brca1<tm1Brn>	involves: 129P2/OlaHsd	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0009504	abnormal mammary gland epithelium morphology	CCO:MP0009504
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0009508	mammary gland ductal carcinoma	CCO:MP0009508
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0001138	abnormal cervical squamous epithelium	CCO:MP0001138
MGI:104537	Brca1	Brca1<tm1Brn>/Brca1<tm1Brn>	involves: 129P2/OlaHsd	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0001885	mammary gland duct hyperplasia	CCO:MP0001885
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:104537	Brca1	"Brca1<tm1Aash>/Brca1<tm1Aash>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000627	abnormal mammary gland morphology	CCO:MP0000627
MGI:104537	Brca1	Brca1<tm4Cxd>/Brca1<tm4Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Chek2<tm1Mak>/Chek2<tm1Mak>,Tg(Wap-cre)11738Mam/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Wap-cre)11738Mam/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	"Brca1<tm1Arge>/Brca1<tm1Arge>,Tg(Hsp70-1-cre)1Arge/0"	involves: 129S/SvEv * C57BL/6J * CBA	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:104537	Brca1	"Brca1<tm1Arge>/Brca1<tm1Thl>,Wap<tm1(cre)Arge>/0"	involves: 129S/SvEv * 129S1/Sv * C57BL/6J	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:104537	Brca1	"Brca1<tm1Thl>/Brca1<tm1Thl>,Wap<tm1(cre)Arge>/0"	involves: 129S1/Sv * C57BL/6J	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:104537	Brca1	"Bard1<tm2Thl>/Bard1<tm2Thl>,Brca1<tm1Thl>/Brca1<tm1Thl>,Wap<tm1(cre)Arge>/0"	involves: 129/Sv * 129S1/Sv * C57BL/6J	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:104537	Brca1	"Brca1<tm2Cxd>/Brca1<+>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0009583	increased keratinocyte proliferation	CCO:MP0009583
MGI:104537	Brca1	Brca1<tm1Thl>/Brca1<tm1Thl>	involves: 129/Sv * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Wap-cre)11738Mam/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Chek2<tm1Mak>/Chek2<tm1Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Chek2<tm1Mak>/Chek2<tm1Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Tg(TcrLCMV)327Sdz/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008083	decreased single-positive T cell number	CCO:MP0008083
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Tg(TcrLCMV)327Sdz/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0006387	abnormal T cell number	CCO:MP0006387
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Tg(TcrLCMV)327Sdz/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Tg(TcrLCMV)327Sdz/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Tg(TcrLCMV)327Sdz/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Tg(TcrLCMV)327Sdz/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(BCL2)36Wehi/?,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(BCL2)36Wehi/?,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Trp53<tm1Brd>/Trp53<+>,Tg(Wap-cre)11738Mam/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008083	decreased single-positive T cell number	CCO:MP0008083
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0006387	abnormal T cell number	CCO:MP0006387
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<tm1Bhk>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<tm1Bhk>	involves: 129P2/OlaHsd * BALB/c * C57BL/6	MP:0000929	open neural tube	CCO:MP0000929
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:104537	Brca1	"Brca1<tm2Cxd>/Brca1<+>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:104537	Brca1	Brca1<tm1.1Brn>/Brca1<tm1.1Brn>	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104537	Brca1	"Brca1<tm1Brn>/Brca1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	"Brca1<tm1Brn>/Brca1<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	"Brca1<tm1Brn>/Brca1<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	"Brca1<tm2Cxd>/Brca1<+>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:104537	Brca1	"Brca1<tm2Cxd>/Brca1<+>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	"Brca1<tm2Cxd>/Brca1<+>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0005276	skin tumor	CCO:MP0005276
MGI:104537	Brca1	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002722	abnormal immune system organ morphology	CCO:MP0002722
MGI:104537	Brca1	"Bard1<tm1Thl>/Bard1<tm1Thl>,Brca1<tm1Arge>/Brca1<tm1Arge>"	involves: 129S/SvEv * 129S1/Sv	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104537	Brca1	"Bard1<tm1Thl>/Bard1<tm1Thl>,Brca1<tm1Arge>/Brca1<tm1Arge>"	involves: 129S/SvEv * 129S1/Sv	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:104537	Brca1	"Bard1<tm1Thl>/Bard1<tm1Thl>,Brca1<tm1Arge>/Brca1<tm1Arge>"	involves: 129S/SvEv * 129S1/Sv	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001693	failure of primitive streak formation	CCO:MP0001693
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<+>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104537	Brca1	"Brca1<tm1Arge>/Brca1<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S6/SvEvTac * C57BL/6	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0005031	abnormal trophoblast layer morphology	CCO:MP0005031
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002582	disorganized extraembryonic tissue	CCO:MP0002582
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001683	absent mesoderm	CCO:MP0001683
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:104537	Brca1	"Brca1<tm1Arge>/Brca1<tm1Arge>,Brca2<tm1Arge>/Brca2<tm1Arge>"	involves: 129S/SvEv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001687	thin endoderm	CCO:MP0001687
MGI:104537	Brca1	"Brca1<tm1Arge>/Brca1<tm1Arge>,Brca2<tm1Arge>/Brca2<tm1Arge>"	involves: 129S/SvEv * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:104537	Brca1	Brca1<tm1Cxd>/Brca1<tm1Cxd>	either: 129S6/SvEvTac-Brca1<tm1Cxd> or (involves: 129S6/SvEvBrd * Black Swiss) or (involves: 129S6/SvEvBrd * C57BL/6)	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:104537	Brca1	Brca1<tm1Cxd>/Brca1<tm1Cxd>	either: 129S6/SvEvTac-Brca1<tm1Cxd> or (involves: 129S6/SvEvBrd * Black Swiss) or (involves: 129S6/SvEvBrd * C57BL/6)	MP:0001684	abnormal axial mesoderm	CCO:MP0001684
MGI:104537	Brca1	Brca1<tm1Cxd>/Brca1<tm1Cxd>	either: 129S6/SvEvTac-Brca1<tm1Cxd> or (involves: 129S6/SvEvBrd * Black Swiss) or (involves: 129S6/SvEvBrd * C57BL/6)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:104537	Brca1	Brca1<tm1Cxd>/Brca1<tm1Cxd>	either: 129S6/SvEvTac-Brca1<tm1Cxd> or (involves: 129S6/SvEvBrd * Black Swiss) or (involves: 129S6/SvEvBrd * C57BL/6)	MP:0002230	abnormal primitive streak formation	CCO:MP0002230
MGI:104537	Brca1	Brca1<tm1Cxd>/Brca1<tm1Cxd>	either: 129S6/SvEvTac-Brca1<tm1Cxd> or (involves: 129S6/SvEvBrd * Black Swiss) or (involves: 129S6/SvEvBrd * C57BL/6)	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:104537	Brca1	Brca1<tm1Cxd>/Brca1<tm1Cxd>	either: 129S6/SvEvTac-Brca1<tm1Cxd> or (involves: 129S6/SvEvBrd * Black Swiss) or (involves: 129S6/SvEvBrd * C57BL/6)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<tm1Mak>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001714	absent trophoblast giant cells	CCO:MP0001714
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001683	absent mesoderm	CCO:MP0001683
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003988	disorganized embryonic tissue	CCO:MP0003988
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104537	Brca1	Brca1<tm2Cxd>/Brca1<tm2Cxd>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0006271	abnormal involution of the mammary gland	CCO:MP0006271
MGI:104537	Brca1	Brca1<tm1Mak>/Brca1<+>	either: (involves: 129P2/OlaHsd * C3H/HeJ) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0006271	abnormal involution of the mammary gland	CCO:MP0006271
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Trp53<tm1Brd>/Trp53<+>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001694	failure to form egg cylinders	CCO:MP0001694
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:104537	Brca1	Brca1<tm1Whl>/Brca1<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:104537	Brca1	Brca1<tm1Cxd>/Brca1<tm1Cxd>	either: 129S6/SvEvTac-Brca1<tm1Cxd> or (involves: 129S6/SvEvBrd * Black Swiss) or (involves: 129S6/SvEvBrd * C57BL/6)	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	MP:0001925	male infertility	CCO:MP0001925
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0009583	increased keratinocyte proliferation	CCO:MP0009583
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0005276	skin tumor	CCO:MP0005276
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	MP:0000585	kinked tail	CCO:MP0000585
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0009583	increased keratinocyte proliferation	CCO:MP0009583
MGI:104537	Brca1	Brca1<tm1Arge>/Brca1<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0003750	mouth tumor	CCO:MP0003750
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0005276	skin tumor	CCO:MP0005276
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0002014	papilloma	CCO:MP0002014
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S6/SvEvTac * C57BL/6	MP:0009583	increased keratinocyte proliferation	CCO:MP0009583
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S6/SvEvTac * C57BL/6	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S6/SvEvTac * C57BL/6	MP:0003750	mouth tumor	CCO:MP0003750
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S6/SvEvTac * C57BL/6	MP:0005276	skin tumor	CCO:MP0005276
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S6/SvEvTac * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Tg(KRT1-5-cre)5132Jlj/0,Tg(KRT5-E2F1)2Dgj/0"	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0003054	spina bifida	CCO:MP0003054
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0000786	abnormal embryonic neuroepithelial layer differentiation	CCO:MP0000786
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0000929	open neural tube	CCO:MP0000929
MGI:104537	Brca1	Brca1<tm1Bhk>/Brca1<tm1Bhk>	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0000914	exencephaly	CCO:MP0000914
MGI:104537	Brca1	Brca1<tm1Arge>/Brca1<+>	involves: 129S/SvEv * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	B6.129-Brca1<tm2Arge>	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	MP:0002095	abnormal skin pigmentation	CCO:MP0002095
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	MP:0000585	kinked tail	CCO:MP0000585
MGI:104537	Brca1	"Brca1<tm1Arge>/Brca1<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	MP:0001925	male infertility	CCO:MP0001925
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	MP:0002095	abnormal skin pigmentation	CCO:MP0002095
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	involves: 129/Sv * C57BL/6J * MF1	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	Brca1<tm1Arge>/Brca1<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:104537	Brca1	Brca1<tm1Arge>/Brca1<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:104537	Brca1	Brca1<tm1Arge>/Brca1<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0003085	abnormal egg cylinder morphology	CCO:MP0003085
MGI:104537	Brca1	Brca1<tm1Arge>/Brca1<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0001683	absent mesoderm	CCO:MP0001683
MGI:104537	Brca1	Brca1<tm1Arge>/Brca1<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0001710	absent amniotic folds	CCO:MP0001710
MGI:104537	Brca1	Brca1<tm2Arge>/Brca1<tm2Arge>	129-Brca1<tm2Arge>	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0004500	increased incidence of ionizing radiation-induced tumors	CCO:MP0004500
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0001260	increased body weight	CCO:MP0001260
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0002022	lymphoma	CCO:MP0002022
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0002676	uterus hyperplasia	CCO:MP0002676
MGI:104537	Brca1	"Brca1<tm2Cxd>/Brca1<tm2Cxd>,Tg(Fshr-cre)1Ldu/0"	involves: C57BL/6J	MP:0002016	ovary cysts	CCO:MP0002016
MGI:104537	Brca1	"Brca1<tm2Cxd>/Brca1<tm2Cxd>,Tg(Fshr-cre)1Ldu/0"	involves: C57BL/6J	MP:0003675	kidney cysts	CCO:MP0003675
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:104537	Brca1	Brca1<tm3Cxd>/Brca1<tm3Cxd>	involves: 129S6/SvEvTac * FVB/N	MP:0000400	abnormal awl hair	CCO:MP0000400
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Tyj>/Trp53<+>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	129S/SvEv-Brca2<tm1Cam>	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0002083	premature death	CCO:MP0002083
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0001926	female infertility	CCO:MP0001926
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0001925	male infertility	CCO:MP0001925
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0004806	absent germ cells	CCO:MP0004806
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0004955	increased thymus weight	CCO:MP0004955
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	129S/SvEv-Brca2<tm1Cam>	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	129S/SvEv-Brca2<tm1Cam>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	129S/SvEv-Brca2<tm1Cam>	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	129S/SvEv-Brca2<tm1Cam>	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:109337	Brca2	Brca2<tm2Mak>/Brca2<tm2Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004024	aneuploidy	CCO:MP0004024
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0006413	increased T cell apoptosis	CCO:MP0006413
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002018	malignant tumors	CCO:MP0002018
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0001829	increased activated T cell number	CCO:MP0001829
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	129S/SvEv-Brca2<tm1Cam>	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Ptch1<tm1Mps>/Ptch1<+>,Trp53<tm1Tyj>/Trp53<+>,Tg(Nes-cre)1Kln/0"	involves: 129 * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Ptch1<tm1Mps>/Ptch1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129 * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:109337	Brca2	Brca2<tm1Brn>/Brca2<tm1Brn>	involves: 129P2/OlaHsd * FVB/N	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:109337	Brca2	Brca2<tm1.1Brn>/Brca2<tm1.1Brn>	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:109337	Brca2	Brca2<tm1.1Brn>/Brca2<tm1.1Brn>	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:109337	Brca2	Brca2<tm1.1Brn>/Brca2<tm1.1Brn>	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0008813	decreased common myeloid progenitor cell number	CCO:MP0008813
MGI:109337	Brca2	Brca2<tm1Cam>/Brca2<tm1Cam>	involves: 129S/SvEv * MF1	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0003992	increased mortality induced by ionizing radiation	CCO:MP0003992
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0001606	impaired hematopoiesis	CCO:MP0001606
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0000694	spleen hypoplasia	CCO:MP0000694
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0001262	decreased body weight	CCO:MP0001262
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0002396	abnormal hematopoietic system morphology/development	CCO:MP0002396
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:109337	Brca2	Brca2<tm1Mbn>/Brca2<tm1Mbn>	C.129P2-Brca2<tm1Mbn>	MP:0000929	open neural tube	CCO:MP0000929
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:109337	Brca2	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Tyj>/Trp53<+>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * BALB/c	MP:0008943	increased sensitivity to induced cell death	CCO:MP0008943
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * C57BL/6N	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * C57BL/6N	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * C57BL/6N	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:109337	Brca2	Brca2<tm1Kamc>/Brca2<tm1Kamc>	involves: 129P2/OlaHsd * C57BL/6N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:109337	Brca2	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:109337	Brca2	Brca2<tm1Mbn>/Brca2<tm1Mbn>	C.129P2-Brca2<tm1Mbn>	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:109337	Brca2	Brca2<tm1Mbn>/Brca2<tm1Mbn>	involves: 129P2/OlaHsd * 129S/SvEv	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:109337	Brca2	Brca2<tm1Mbn>/Brca2<+>	involves: 129P2/OlaHsd * 129S/SvEv	MP:0002066	abnormal motor capabilities/coordination/movement	CCO:MP0002066
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:109337	Brca2	"Brca2<tm1Kamc>/Brca2<tm1Kamc>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0006079	stomach tumor	CCO:MP0006079
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0004833	ovary atrophy	CCO:MP0004833
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001140	abnormal vagina epithelium morphology	CCO:MP0001140
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001132	absent mature ovarian follicles	CCO:MP0001132
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:109337	Brca2	Brca2<tm1Mbn>/Brca2<tm1Mbn>	C.129P2-Brca2<tm1Mbn>	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0000639	abnormal adrenal gland morphology	CCO:MP0000639
MGI:109337	Brca2	Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:109337	Brca2	Brca2<tm1Mbn>/Brca2<+>	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0000639	abnormal adrenal gland morphology	CCO:MP0000639
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0004894	uterus atrophy	CCO:MP0004894
MGI:109337	Brca2	"Brca2<tm1Kamc>/Brca2<tm1Kamc>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:109337	Brca2	"Brca2<tm1Kamc>/Brca2<tm1Kamc>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:109337	Brca2	"Brca2<tm1Kamc>/Brca2<tm1Kamc>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:109337	Brca2	"Apc<Min>/Apc<+>,Brca2<tm1Mbn>/Brca2<+>"	B6.Cg-Brca2<tm1Mbn> Apc<Min>	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:109337	Brca2	"Brca2<tm2Arge>/Brca2<tm2Arge>,Wap<tm1(cre)Arge>/Wap<tm1(cre)Arge>"	involves: 129S1/Sv * C57BL/6	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<+>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:109337	Brca2	Brca2<tm1Brd>/Brca2<tm1Brd>	involves: 129S7/SvEvBrd	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:109337	Brca2	Brca2<tm1Brd>/Brca2<tm1Brd>	involves: 129S7/SvEvBrd	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:109337	Brca2	Brca2<tm1Brd>/Brca2<tm1Brd>	involves: 129S7/SvEvBrd	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:109337	Brca2	Brca2<tm1Brd>/Brca2<tm1Brd>	involves: 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109337	Brca2	"Brca2<tm1Arge>/Brca2<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:109337	Brca2	"Brca2<tm1Arge>/Brca2<tm2Arge>,Wap<tm1(cre)Arge>/Wap<+>"	involves: 129S/SvEv * C57BL/6	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002089	abnormal postnatal growth/weight/body size	CCO:MP0002089
MGI:109337	Brca2	Brca2<tm1Arge>/Brca2<tm2Arge>	involves: 129S/SvEv * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:109337	Brca2	Brca2<tm1Hst>/Brca2<tm2Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:109337	Brca2	Brca2<tm1Hst>/Brca2<tm2Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:109337	Brca2	Brca2<tm2Hst>/Brca2<tm2Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109337	Brca2	Brca2<tm1Hst>/Brca2<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005044	sepsis	CCO:MP0005044
MGI:109337	Brca2	Brca2<tm1Hst>/Brca2<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:109337	Brca2	Brca2<tm1Hst>/Brca2<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:109337	Brca2	Brca2<tm1Brd>/Brca2<+>	involves: 129S7/SvEvBrd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:109337	Brca2	Brca2<tm1Mak>/Brca2<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002088	abnormal embryonic growth/weight/body size	CCO:MP0002088
MGI:109337	Brca2	Brca2<tm1Arge>/Brca2<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:109337	Brca2	Brca2<tm1Arge>/Brca2<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109337	Brca2	Brca2<tm1Hst>/Brca2<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:109337	Brca2	"Brca1<tm1Arge>/Brca1<tm1Arge>,Brca2<tm1Arge>/Brca2<tm1Arge>"	involves: 129S/SvEv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109337	Brca2	"Brca1<tm1Arge>/Brca1<tm1Arge>,Brca2<tm1Arge>/Brca2<tm1Arge>"	involves: 129S/SvEv * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:109337	Brca2	"Brca2<tm1Arge>/Brca2<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109337	Brca2	"Brca2<tm1Arge>/Brca2<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000914	exencephaly	CCO:MP0000914
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002083	premature death	CCO:MP0002083
MGI:109337	Brca2	Brca2<tm1Mak>/Brca2<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:109337	Brca2	Brca2<tm1Mak>/Brca2<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/10	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<+>	involves: 129S2/SvPas * C57BL/10	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002111	abnormal tail morphology	CCO:MP0002111
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002096	abnormal skin condition/ morphology	CCO:MP0002096
MGI:109337	Brca2	Brca2<tm1Cbl>/Brca2<tm1Cbl>	involves: 129S2/SvPas * C57BL/6 * DBA	MP:0002088	abnormal embryonic growth/weight/body size	CCO:MP0002088
MGI:109337	Brca2	Brca2<tm1Arge>/Brca2<tm1Arge>	involves: 129S/SvEv * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:109337	Brca2	Brca2<tm1Mak>/Brca2<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:109337	Brca2	Brca2<tm1Hst>/Brca2<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109337	Brca2	Brca2<tm1Mhun>/Brca2<+>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0004502	decreased incidence of chemically-induced tumors	CCO:MP0004502
MGI:109337	Brca2	Brca2<tm1Mhun>/Brca2<+>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:109337	Brca2	Brca2<tm1Mhun>/Brca2<+>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:109337	Brca2	Brca2<tm1Mhun>/Brca2<tm1Mhun>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:109337	Brca2	Brca2<tm1Mhun>/Brca2<+>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002882	abnormal neuron morphology	CCO:MP0002882
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000783	abnormal forebrain morphology	CCO:MP0000783
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005498	hyporesponsive to tactile stimuli	CCO:MP0005498
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:2685946	Brsk1	Brsk1<tm1Jrs>/Brsk1<tm1Jrs>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000822	abnormal brain ventricle morphology	CCO:MP0000822
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008442	disorganized cortical plate	CCO:MP0008442
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003651	abnormal axon outgrowth	CCO:MP0003651
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008440	abnormal subplate morphology	CCO:MP0008440
MGI:2685946	Brsk1	"Brsk1<tm1Jrs>/Brsk1<tm1Jrs>,Brsk2<tm1Jrs>/Brsk2<tm1Jrs>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005156	bradykinesia	CCO:MP0005156
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002746	abnormal semilunar valve morphology	CCO:MP0002746
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002747	abnormal aortic valve morphology	CCO:MP0002747
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0005598	decreased ventricle muscle contractility	CCO:MP0005598
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003141	cardiac fibrosis	CCO:MP0003141
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003869	ectopic cartilage	CCO:MP0003869
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002745	abnormal atrioventricular valve morphology	CCO:MP0002745
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001855	atrial thrombosis	CCO:MP0001855
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0004063	dilated heart left atrium	CCO:MP0004063
MGI:99439	Btc	Btc<tm1Dcl>/Btc<tm1Dcl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:99439	Btc	"Btc<tm1Dcl>/Btc<tm1Dcl>,Hbegf<tm1Dcl>/Hbegf<tm1Dcl>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:109532	Btg3	Btg3<tm1Tya>/Btg3<tm1Tya>	involves: 129P2/OlaHsd * C57BL/6J	MP:0009585	ectopic bone formation	CCO:MP0009585
MGI:109532	Btg3	Btg3<tm1Tya>/Btg3<tm1Tya>	involves: 129P2/OlaHsd * C57BL/6J	MP:0008014	lung tumor	CCO:MP0008014
MGI:109532	Btg3	Btg3<tm1Tya>/Btg3<tm1Tya>	involves: 129P2/OlaHsd * C57BL/6J	MP:0008714	lung carcinoma	CCO:MP0008714
MGI:109532	Btg3	Btg3<tm1Tya>/Btg3<tm1Tya>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1338871	Btrc	Btrc<tm1Kin>/Btrc<tm1Kin>	involves: C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1338871	Btrc	Btrc<tm1Kin>/Btrc<tm1Kin>	involves: C57BL/6	MP:0002619	abnormal lymphocyte morphology	CCO:MP0002619
MGI:1338871	Btrc	Btrc<tm1Kin>/Btrc<tm1Kin>	involves: C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1338871	Btrc	Btrc<tm1Kin>/Btrc<tm1Kin>	involves: C57BL/6	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:1338871	Btrc	Btrc<tm1Kin>/Btrc<tm1Kin>	involves: C57BL/6	MP:0004025	polyploidy	CCO:MP0004025
MGI:1338871	Btrc	Btrc<tm1Paga>/Btrc<tm1Paga>	involves: 129S2/SvPas	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1338871	Btrc	Btrc<tm1Paga>/Btrc<tm1Paga>	involves: 129S2/SvPas	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1338871	Btrc	Btrc<tm1Paga>/Btrc<tm1Paga>	involves: 129S2/SvPas	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1338871	Btrc	Btrc<tm1Paga>/Btrc<tm1Paga>	involves: 129S2/SvPas	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004759	decreased mitotic index	CCO:MP0004759
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004201	fetal growth retardation	CCO:MP0004201
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001925	male infertility	CCO:MP0001925
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1.1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1100510	Bub1	"Bub1<tm1Ssta>/Bub1<tm1.1Ssta>,Tg(CAG-cre/Esr1)5Amc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1100510	Bub1	Bub1<tm1.1Ssta>/Bub1<tm1.1Ssta>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:1100510	Bub1	Bub1<tm1Tvd>/Bub1<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<+>	involves: 129/Sv * C57BL/6	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1100510	Bub1	Bub1<Gt(XG453)Byg>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	B6.129P2-Bub1<tm1.1Tvd>	MP:0009674	decreased birth weight	CCO:MP0009674
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	B6.129P2-Bub1<tm1.1Tvd>	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	B6.129P2-Bub1<tm1.1Tvd>	MP:0001577	anemia	CCO:MP0001577
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	B6.129P2-Bub1<tm1.1Tvd>	MP:0001654	hepatic necrosis	CCO:MP0001654
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	B6.129P2-Bub1<tm1.1Tvd>	MP:0000603	pale liver	CCO:MP0000603
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	B6.129P2-Bub1<tm1.1Tvd>	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0008019	liver tumor	CCO:MP0008019
MGI:1100510	Bub1	Bub1<tm1.1Tvd>/Bub1<tm1.1Tvd>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0008014	lung tumor	CCO:MP0008014
MGI:1100510	Bub1	Bub1<tm1.1Jvd>/Bub1<tm1.1Jvd>	involves: 129/Sv * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1100510	Bub1	Bub1<tm2Jvd>/Bub1<tm2Jvd>	involves: 129/Sv * C57BL/6	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:1100510	Bub1	Bub1<Gt(XG453)Byg>/Bub1<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003718	maternal effect	CCO:MP0003718
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<+>	involves: 129S6/SvEvTac	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1333889	Bub1b	Bub1b<tm1.1Jvd>/Bub1b<+>	involves: 129S6/SvEvTac	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<+>	involves: 129S4/SvJae	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<+>	involves: 129S4/SvJae	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<+>	involves: 129S4/SvJae * C57BL/6	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<+>	involves: 129S4/SvJae * C57BL/6	MP:0000239	absent common myeloid progenitor cells	CCO:MP0000239
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<+>	involves: 129S4/SvJae * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<+>	involves: 129S4/SvJae * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<Gt(neo-btk)1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<Gt(neo-btk)1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<Gt(neo-btk)1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<+>	involves: 129S4/SvJae	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:1333889	Bub1b	Bub1b<Gt(neo-btk)1Dai>/Bub1b<+>	involves: 129S4/SvJae * C57BL/6	MP:0000229	abnormal megakaryocyte differentiation	CCO:MP0000229
MGI:1333889	Bub1b	Bub1b<tm1.1Jvd>/Bub1b<tm1.1Jvd>	involves: 129S6/SvEvTac	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0000162	lordosis	CCO:MP0000162
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0001792	impaired wound healing	CCO:MP0001792
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0002083	premature death	CCO:MP0002083
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1.1Jvd>	involves: 129S6/SvEvTac	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0005150	cachexia	CCO:MP0005150
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0008844	decreased subcutaneous adipose tissue amount	CCO:MP0008844
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0008007	abnormal cellular replicative senescence	CCO:MP0008007
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0001304	cataracts	CCO:MP0001304
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0002269	muscular atrophy	CCO:MP0002269
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0001926	female infertility	CCO:MP0001926
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0001925	male infertility	CCO:MP0001925
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0005454	decreased adipose tissue amount	CCO:MP0005454
MGI:1333889	Bub1b	Bub1b<tm1Jvd>/Bub1b<tm1Jvd>	involves: 129S6/SvEvTac	MP:0001244	thin dermal layer	CCO:MP0001244
MGI:1343463	Bub3	Bub3<tm1Jvd>/Bub3<tm1Jvd>	Not Specified	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1343463	Bub3	Bub3<tm1Jvd>/Bub3<+>	Not Specified	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1343463	Bub3	Bub3<tm1Jvd>/Bub3<+>	Not Specified	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1343463	Bub3	Bub3<tm1Jvd>/Bub3<+>	Not Specified	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0000160	kyphosis	CCO:MP0000160
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0000749	muscle degeneration	CCO:MP0000749
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0001244	thin dermal layer	CCO:MP0001244
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0001304	cataracts	CCO:MP0001304
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0001263	weight loss	CCO:MP0001263
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0000162	lordosis	CCO:MP0000162
MGI:1343463	Bub3	Bub3<tm1Jvd>/Bub3<+>	Not Specified	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0002269	muscular atrophy	CCO:MP0002269
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0003786	premature aging	CCO:MP0003786
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0005454	decreased adipose tissue amount	CCO:MP0005454
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0005150	cachexia	CCO:MP0005150
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1343463	Bub3	"Bub3<tm1Jvd>/Bub3<+>,Rae1<tm1Jvd>/Rae1<+>"	Not Specified	MP:0008007	abnormal cellular replicative senescence	CCO:MP0008007
MGI:1343463	Bub3	Bub3<tm1Khac>/Bub3<tm1Khac>	either: 129P/Ola or 129S1/Sv	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1343463	Bub3	Bub3<tm1Khac>/Bub3<tm1Khac>	either: 129P/Ola or 129S1/Sv	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:1343463	Bub3	Bub3<tm1Khac>/Bub3<tm1Khac>	either: 129P/Ola or 129S1/Sv	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:1343463	Bub3	Bub3<tm1Khac>/Bub3<tm1Khac>	either: 129P/Ola or 129S1/Sv	MP:0004965	inner cell mass degeneration	CCO:MP0004965
MGI:1927065	Cables1	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	MP:0001123	dilated uterus	CCO:MP0001123
MGI:1927065	Cables1	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1927065	Cables1	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	MP:0004868	endometrial carcinoma	CCO:MP0004868
MGI:1927065	Cables1	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	MP:0004896	abnormal endometrium morphology	CCO:MP0004896
MGI:1927065	Cables1	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	MP:0004906	enlarged uterus	CCO:MP0004906
MGI:1927065	Cables1	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	MP:0009092	endometrium hyperplasia	CCO:MP0009092
MGI:1927065	Cables1	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	MP:0009094	abnormal endometrial gland morphology	CCO:MP0009094
MGI:1927065	Cables1	Cables1<tm1Lrz>/Cables1<tm1Lrz>	involves: 129S1/Sv	MP:0001935	decreased litter size	CCO:MP0001935
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0003052	omphalocele	CCO:MP0003052
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0004567	decreased myocardial fiber number	CCO:MP0004567
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0000295	poorly developed ventricular trabeculae	CCO:MP0000295
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0005440	increased glycogen level	CCO:MP0005440
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0004057	thin myocardial compact layer	CCO:MP0004057
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0004090	abnormal sarcomere morphology	CCO:MP0004090
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0004091	abnormal Z lines	CCO:MP0004091
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0006267	abnormal intercalated disc morphology	CCO:MP0006267
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0004231	abnormal calcium ion homeostasis	CCO:MP0004231
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0002188	small heart	CCO:MP0002188
MGI:88252	Calr	Calr<tm1Mlk>/Calr<tm1Mlk>	involves: 129S4/SvJae * C57BL/6J	MP:0000278	abnormal myocardial fiber morphology	CCO:MP0000278
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0003566	abnormal cell adhesion	CCO:MP0003566
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0003222	increased cardiomyocyte apoptosis	CCO:MP0003222
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0000914	exencephaly	CCO:MP0000914
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0003052	omphalocele	CCO:MP0003052
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0002952	ventricular cardiomyopathy	CCO:MP0002952
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0000296	absent ventricular trabeculae	CCO:MP0000296
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0000929	open neural tube	CCO:MP0000929
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:88252	Calr	Calr<tm1Star>/Calr<tm1Star>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL)	MP:0003091	abnormal cell migration	CCO:MP0003091
MGI:88256	Camk2a	Camk2a<tm2Sva>/Camk2a<tm2Sva>	B6.129P2-Camk2a<tm2Sva>	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:88256	Camk2a	Camk2a<tm1Sva>/Camk2a<tm1Sva>	involves: 129P2/OlaHsd * BALB/c	MP:0001364	decreased anxiety-related response	CCO:MP0001364
MGI:88256	Camk2a	Camk2a<tm1Mllr>/Camk2a<tm1Mllr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002207	abnormal long term potentiation	CCO:MP0002207
MGI:88256	Camk2a	Camk2a<tm1Mllr>/Camk2a<tm1Mllr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001454	abnormal cued conditioning behavior	CCO:MP0001454
MGI:88256	Camk2a	Camk2a<tm1Mllr>/Camk2a<tm1Mllr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:88256	Camk2a	Camk2a<tm1Mllr>/Camk2a<tm1Mllr>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88256	Camk2a	Camk2a<tm5Sva>/Camk2a<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm5Sva>/Camk2a<tm5Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001898	abnormal long term depression	CCO:MP0001898
MGI:88256	Camk2a	Camk2a<tm1Mllr>/Camk2a<tm1Mllr>	B6.129-Camk2a<tm1Mllr>	MP:0001454	abnormal cued conditioning behavior	CCO:MP0001454
MGI:88256	Camk2a	Camk2a<tm1Mllr>/Camk2a<tm1Mllr>	B6.129-Camk2a<tm1Mllr>	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:88256	Camk2a	Camk2a<tm2Sva>/Camk2a<tm2Sva>	B6.129P2-Camk2a<tm2Sva>	MP:0000973	abnormal cutaneous/subcutaneous mechanoreceptor morphology	CCO:MP0000973
MGI:88256	Camk2a	Camk2a<tm1Mllr>/Camk2a<tm1Mllr>	B6.129-Camk2a<tm1Mllr>	MP:0002801	abnormal long term object recognition memory	CCO:MP0002801
MGI:88256	Camk2a	Camk2a<tm1Sva>/Camk2a<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006060	increased cerebral infarction size	CCO:MP0006060
MGI:88256	Camk2a	Camk2a<tm1Sva>/Camk2a<tm1Sva>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006060	increased cerebral infarction size	CCO:MP0006060
MGI:88256	Camk2a	Camk2a<tm1Sva>/Camk2a<tm1Sva>	involves: 129P2/OlaHsd	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm1Sva>/Camk2a<tm1Sva>	involves: 129P2/OlaHsd	MP:0001475	reduced long term depression	CCO:MP0001475
MGI:88256	Camk2a	Camk2a<tm1Sva>/Camk2a<tm1Sva>	involves: 129P2/OlaHsd	MP:0002206	abnormal CNS synaptic transmission	CCO:MP0002206
MGI:88256	Camk2a	Camk2a<tm1Sva>/Camk2a<tm1Sva>	involves: 129P2/OlaHsd * BALB/c	MP:0002920	decreased paired-pulse facilitation	CCO:MP0002920
MGI:88256	Camk2a	Camk2a<tm2Sva>/Camk2a<tm2Sva>	B6.129P2-Camk2a<tm2Sva>	MP:0008143	abnormal dendrite morphology	CCO:MP0008143
MGI:88256	Camk2a	Camk2a<tm1Sva>/Camk2a<tm1Sva>	involves: 129P2/OlaHsd * BALB/c	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm5Sva>/Camk2a<tm5Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:88256	Camk2a	Camk2a<tm5Sva>/Camk2a<tm5Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm3Sva>/Camk2a<tm3Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:88256	Camk2a	Camk2a<tm2Sva>/Camk2a<tm2Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm3Sva>/Camk2a<tm3Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm3Sva>/Camk2a<tm3Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002912	abnormal excitatory postsynaptic potential	CCO:MP0002912
MGI:88256	Camk2a	Camk2a<tm3Sva>/Camk2a<tm3Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004769	abnormal synaptic vesicle morphology	CCO:MP0004769
MGI:88256	Camk2a	Camk2a<tm3Sva>/Camk2a<tm3Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004792	abnormal synaptic vesicle number	CCO:MP0004792
MGI:88256	Camk2a	Camk2a<tm3Sva>/Camk2a<tm3Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004859	abnormal synaptic plasticity	CCO:MP0004859
MGI:88256	Camk2a	Camk2a<tm4Sva>/Camk2a<tm4Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003008	enhanced long term potentiation	CCO:MP0003008
MGI:88256	Camk2a	Camk2a<tm5Sva>/Camk2a<tm5Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm1Mllr>/Camk2a<tm1Mllr>	B6.129-Camk2a<tm1Mllr>	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88256	Camk2a	Camk2a<tm3Sva>/Camk2a<tm3Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88256	Camk2a	Camk2a<tm3Sva>/Camk2a<tm3Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm4Sva>/Camk2a<tm4Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0002064	seizures	CCO:MP0002064
MGI:88256	Camk2a	Camk2a<tm4Sva>/Camk2a<tm4Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88256	Camk2a	Camk2a<tm2Sva>/Camk2a<tm2Sva>	B6.129P2-Camk2a<tm2Sva>	MP:0002910	abnormal excitatory postsynaptic currents	CCO:MP0002910
MGI:88256	Camk2a	Camk2a<tm4Sva>/Camk2a<tm4Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:88256	Camk2a	Camk2a<tm4Sva>/Camk2a<tm4Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0002207	abnormal long term potentiation	CCO:MP0002207
MGI:88256	Camk2a	Camk2a<tm4Sva>/Camk2a<tm4Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0003858	enhanced coordination	CCO:MP0003858
MGI:88256	Camk2a	Camk2a<tm5Sva>/Camk2a<tm5Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0002064	seizures	CCO:MP0002064
MGI:88256	Camk2a	Camk2a<tm5Sva>/Camk2a<tm5Sva>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0002083	premature death	CCO:MP0002083
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0001462	abnormal avoidance learning behavior	CCO:MP0001462
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0001399	hyperactivity	CCO:MP0001399
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0002882	abnormal neuron morphology	CCO:MP0002882
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<+>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<+>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0002083	premature death	CCO:MP0002083
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<+>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0000951	sporadic seizures	CCO:MP0000951
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<+>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0001399	hyperactivity	CCO:MP0001399
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0008431	abnormal short term spatial reference memory	CCO:MP0008431
MGI:88256	Camk2a	Camk2a<tm1.1Oyam>/Camk2a<tm1.1Oyam>	either: B6.Cg-Camk2a<tm1.1Oyam> or (involves: C57BL/6 * CBA * ICR)	MP:0000951	sporadic seizures	CCO:MP0000951
MGI:88256	Camk2a	"Camk2a<tm1Vyb>/Camk2a<tm1Vyb>,Tg(Grik4-cre)G32-4Stl/0"	involves: C57BL/6	MP:0003635	abnormal synaptic transmission	CCO:MP0003635
MGI:88256	Camk2a	"Camk2a<tm1Vyb>/Camk2a<tm1Vyb>,Tg(Grik4-cre)G32-4Stl/0"	involves: C57BL/6	MP:0002206	abnormal CNS synaptic transmission	CCO:MP0002206
MGI:1341265	Camk2d	Camk2d<tm1.2Eno>/Camk2d<tm1.2Eno>	involves: 129S/SvEvBrd * C57BL/6 * CD-1 * SJL	MP:0004486	decreased response of heart to induced stress	CCO:MP0004486
MGI:107739	Casp3	Casp3<tm1Mak>/Casp3<tm1Mak>	B6.129P2-Casp3<tm1Mak>	MP:0002083	premature death	CCO:MP0002083
MGI:107739	Casp3	Casp3<tm1Mak>/Casp3<tm1Mak>	B6.129P2-Casp3<tm1Mak>	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:107739	Casp3	"Casp3<tm1Mak>/Casp3<tm1Mak>,Tg(TcrLCMV)327Sdz/0"	B6.Cg-Casp3<tm1Mak> Tg(TcrLCMV)327Sdz	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:107739	Casp3	"Casp3<tm1Mak>/Casp3<tm1Mak>,Tg(TcrLCMV)327Sdz/0"	B6.Cg-Casp3<tm1Mak> Tg(TcrLCMV)327Sdz	MP:0005010	abnormal CD8-positive T cell morphology	CCO:MP0005010
MGI:107739	Casp3	"Casp3<tm1Mak>/Casp3<tm1Mak>,Tg(TcrLCMV)327Sdz/0"	B6.Cg-Casp3<tm1Mak> Tg(TcrLCMV)327Sdz	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:107739	Casp3	Casp3<tm1Mak>/Casp3<tm1Mak>	B6.129P2-Casp3<tm1Mak>	MP:0001876	decreased inflammatory response	CCO:MP0001876
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<tm1Flv>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0005294	abnormal heart ventricle morphology	CCO:MP0005294
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<tm1Flv>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0009542	decreased thymocyte apoptosis	CCO:MP0009542
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<tm1Flv>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0003140	dilated atria	CCO:MP0003140
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<tm1Flv>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0000914	exencephaly	CCO:MP0000914
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<tm1Flv>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<tm1Flv>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<tm1Flv>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<+>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0009542	decreased thymocyte apoptosis	CCO:MP0009542
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<+>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<+>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp7<tm1Flv>/Casp7<tm1Flv>"	B6.129S-Casp3<tm1Flv> Casp7<tm1Flv>	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0009346	decreased cancellous bone thickness	CCO:MP0009346
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000872	abnormal external granule cell layer morphology	CCO:MP0000872
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000830	abnormal diencephalon morphology	CCO:MP0000830
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0005201	abnormal retinal pigment epithelium morphology	CCO:MP0005201
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0003733	abnormal retinal inner nuclear layer morphology	CCO:MP0003733
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0004268	abnormal optic stalk morphology	CCO:MP0004268
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000783	abnormal forebrain morphology	CCO:MP0000783
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000889	abnormal cerebellar molecular layer	CCO:MP0000889
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0003843	abnormal sagittal suture morphology	CCO:MP0003843
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:107739	Casp3	Casp3<tm1Kin>/Casp3<tm1Kin>	B6.129P2-Casp3<tm1Kin>	MP:0004737	absent distortion product otoacoustic emissions	CCO:MP0004737
MGI:107739	Casp3	Casp3<tm1Kin>/Casp3<tm1Kin>	B6.129P2-Casp3<tm1Kin>	MP:0004765	decreased brainstem auditory evoked potential	CCO:MP0004765
MGI:107739	Casp3	Casp3<tm1Kin>/Casp3<tm1Kin>	B6.129P2-Casp3<tm1Kin>	MP:0006358	absent pinna reflex	CCO:MP0006358
MGI:107739	Casp3	Casp3<tm1Kin>/Casp3<tm1Kin>	B6.129P2-Casp3<tm1Kin>	MP:0004398	cochlear inner hair cell degeneration	CCO:MP0004398
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0005277	abnormal brainstem morphology	CCO:MP0005277
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:107739	Casp3	Casp3<tm1Kin>/Casp3<tm1Kin>	B6.129P2-Casp3<tm1Kin>	MP:0004404	cochlear outer hair cell degeneration	CCO:MP0004404
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000168	abnormal bone marrow development	CCO:MP0000168
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0002113	abnormal skeleton development	CCO:MP0002113
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000854	abnormal cerebellum development	CCO:MP0000854
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000919	cranioschisis	CCO:MP0000919
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0001541	abnormal osteoclast physiology	CCO:MP0001541
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000057	abnormal osteogenesis	CCO:MP0000057
MGI:107739	Casp3	Casp3<tm1Kin>/Casp3<tm1Kin>	B6.129P2-Casp3<tm1Kin>	MP:0002857	cochlear ganglion degeneration	CCO:MP0002857
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	involves: 129S1/Sv * C57BL/6	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0001304	cataracts	CCO:MP0001304
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0002102	abnormal ear morphology	CCO:MP0002102
MGI:107739	Casp3	Casp3<tm1Dsp>/Casp3<tm1Dsp>	involves: 129X1/SvJ	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:107739	Casp3	Casp3<tm1Dsp>/Casp3<tm1Dsp>	involves: 129X1/SvJ	MP:0002083	premature death	CCO:MP0002083
MGI:107739	Casp3	Casp3<tm1Dsp>/Casp3<tm1Dsp>	involves: 129X1/SvJ	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0004763	absent brainstem auditory evoked potential	CCO:MP0004763
MGI:107739	Casp3	Casp3<tm1Dsp>/Casp3<tm1Dsp>	involves: 129X1/SvJ	MP:0000819	abnormal olfactory bulb morphology	CCO:MP0000819
MGI:107739	Casp3	Casp3<tm1Dsp>/Casp3<tm1Dsp>	involves: 129X1/SvJ	MP:0008789	abnormal olfactory epithelium morphology	CCO:MP0008789
MGI:107739	Casp3	Casp3<tm1Dsp>/Casp3<tm1Dsp>	involves: 129X1/SvJ	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0000042	abnormal organ of Corti	CCO:MP0000042
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0004527	abnormal outer hair cell stereociliary bundle morphology	CCO:MP0004527
MGI:107739	Casp3	Casp3<tm1Dsp>/Casp3<tm1Dsp>	involves: 129X1/SvJ	MP:0002739	abnormal olfactory bulb development	CCO:MP0002739
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp6<tm1Flv>/Casp6<tm1Flv>"	involves: 129S1/Sv * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Pde6b<rd1>/Pde6b<rd1>"	involves: 129S1 * C3H/FeJ * C57BL/6J	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<+>	involves: 129S1/Sv * C57BL/6J	MP:0003843	abnormal sagittal suture morphology	CCO:MP0003843
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<+>	involves: 129S1/Sv * C57BL/6J	MP:0002998	abnormal bone remodeling	CCO:MP0002998
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<+>	involves: 129S1/Sv * C57BL/6J	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Pde6b<rd1>/Pde6b<rd1>"	involves: 129S1 * C3H/FeJ * C57BL/6J	MP:0008453	decreased retinal rod cell number	CCO:MP0008453
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Pde6b<rd1>/Pde6b<rd1>"	involves: 129S1 * C3H/FeJ * C57BL/6J	MP:0008517	thick retinal outer nuclear layer	CCO:MP0008517
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<+>	involves: 129S1/Sv * C57BL/6J	MP:0000919	cranioschisis	CCO:MP0000919
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<+>	involves: 129S1/Sv * C57BL/6J	MP:0000057	abnormal osteogenesis	CCO:MP0000057
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp6<tm1Flv>/Casp6<tm1Flv>"	involves: 129S1/Sv * C57BL/6J	MP:0001297	microphthalmia	CCO:MP0001297
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0004398	cochlear inner hair cell degeneration	CCO:MP0004398
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp6<tm1Flv>/Casp6<tm1Flv>"	involves: 129S1/Sv * C57BL/6J	MP:0001304	cataracts	CCO:MP0001304
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0000032	cochlear degeneration	CCO:MP0000032
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0004765	decreased brainstem auditory evoked potential	CCO:MP0004765
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0004528	fused outer hair cell stereocilia	CCO:MP0004528
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Pde6b<rd1>/Pde6b<rd1>"	involves: 129S1 * C3H/FeJ * C57BL/6J	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0004404	cochlear outer hair cell degeneration	CCO:MP0004404
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0003237	abnormal lens epithelium morphology	CCO:MP0003237
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0002857	cochlear ganglion degeneration	CCO:MP0002857
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0001967	deafness	CCO:MP0001967
MGI:107739	Casp3	"Casp3<tm1Flv>/Casp3<tm1Flv>,Casp6<tm1Flv>/Casp6<tm1Flv>"	involves: 129S1/Sv * C57BL/6J	MP:0001293	anophthalmia	CCO:MP0001293
MGI:107739	Casp3	Casp3<tm1Flv>/Casp3<tm1Flv>	B6.129S1-Casp3<tm1Flv>	MP:0008868	abnormal granulosa cell morphology	CCO:MP0008868
MGI:108042	Ccna1	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:108042	Ccna1	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:108042	Ccna1	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:108042	Ccna1	Ccna1<tm1Djw>/Ccna1<tm1Djw>	involves: 129S7/SvEvBrd	MP:0001925	male infertility	CCO:MP0001925
MGI:108042	Ccna1	Ccna1<tm1Coll>/Ccna1<+>	either: 129S/SvEv or (involves: 129S/SvEv * MF1)	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:108042	Ccna1	Ccna1<tm1Coll>/Ccna1<+>	either: 129S/SvEv or (involves: 129S/SvEv * MF1)	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:108042	Ccna1	Ccna1<tm1Coll>/Ccna1<+>	either: 129S/SvEv or (involves: 129S/SvEv * MF1)	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:108042	Ccna1	Ccna1<tm1Coll>/Ccna1<tm1Coll>	involves: 129S/SvEv * MF1	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:108042	Ccna1	Ccna1<tm1Coll>/Ccna1<tm1Coll>	involves: 129S/SvEv * MF1	MP:0001925	male infertility	CCO:MP0001925
MGI:108042	Ccna1	Ccna1<tm1Coll>/Ccna1<tm1Coll>	involves: 129S/SvEv * MF1	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:108069	Ccna2	Ccna2<tm1Sot>/Ccna2<tm1Sot>	either: (involves: 129P2/OlaHsd * BALB/c) or (involves: 129X1/SvJ * BALB/c)	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:108069	Ccna2	Ccna2<tm1Sot>/Ccna2<tm1Sot>	either: (involves: 129P2/OlaHsd * BALB/c) or (involves: 129X1/SvJ * BALB/c)	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:88302	Ccnb1	Ccnb1<tm1Thnt>/Ccnb1<tm1Thnt>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0005159	azoospermia	CCO:MP0005159
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0008967	absent chiasmata formation	CCO:MP0008967
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0001924	infertility	CCO:MP0001924
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0001930	abnormal meiosis	CCO:MP0001930
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0001125	abnormal oocyte morphology	CCO:MP0001125
MGI:2685134	Ccnb1ip1	Ccnb1ip1<mei4>/Ccnb1ip1<mei4>	involves: C3HeB/FeJ * C57BL/6J	MP:0001147	small testis	CCO:MP0001147
MGI:88311	Ccnb2	Ccnb2<tm1Thnt>/Ccnb2<tm1Thnt>	involves: 129P2/OlaHsd * C57BL/6	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:88311	Ccnb2	Ccnb2<tm1Thnt>/Ccnb2<tm1Thnt>	involves: 129P2/OlaHsd * C57BL/6	MP:0000706	small thymus	CCO:MP0000706
MGI:88311	Ccnb2	Ccnb2<tm1Thnt>/Ccnb2<tm1Thnt>	involves: 129P2/OlaHsd * C57BL/6	MP:0001935	decreased litter size	CCO:MP0001935
MGI:88311	Ccnb2	Ccnb2<tm1Thnt>/Ccnb2<tm1Thnt>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:88311	Ccnb2	Ccnb2<tm1Thnt>/Ccnb2<tm1Thnt>	involves: 129P2/OlaHsd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88313	Ccnd1	Ccnd1<tm2Phin>/Ccnd1<tm2Phin>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6J)	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas * C57BL/6	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:88313	Ccnd1	Ccnd1<tm1(CCNE)Pisc>/Ccnd1<tm1(CCNE)Pisc>	involves: 129/Sv * C57BL/6	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:88313	Ccnd1	Ccnd1<tm1(CCNE)Pisc>/Ccnd1<tm1(CCNE)Pisc>	involves: 129/Sv * C57BL/6	MP:0005551	abnormal eye electrophysiology	CCO:MP0005551
MGI:88313	Ccnd1	Ccnd1<tm1(CCNE)Pisc>/Ccnd1<tm1(CCNE)Pisc>	involves: 129/Sv * C57BL/6	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas * C57BL/6	MP:0001513	limb grasping	CCO:MP0001513
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas * C57BL/6	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas * C57BL/6	MP:0005551	abnormal eye electrophysiology	CCO:MP0005551
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0004808	abnormal hematopoietic stem cell morphology	CCO:MP0004808
MGI:88313	Ccnd1	Ccnd1<tm1(Ccnd2)Pisc>/Ccnd1<tm1(Ccnd2)Pisc>	involves: 129S4/SvJae	MP:0005551	abnormal eye electrophysiology	CCO:MP0005551
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000875	abnormal cerebellar Purkinje cell layer	CCO:MP0000875
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	MP:0001513	limb grasping	CCO:MP0001513
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0001577	anemia	CCO:MP0001577
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	MP:0005551	abnormal eye electrophysiology	CCO:MP0005551
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	MP:0001882	abnormal lactation	CCO:MP0001882
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:88313	Ccnd1	"Apc<Min>/Apc<+>,Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>"	involves: C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000852	small cerebellum	CCO:MP0000852
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0001436	abnormal suckling behavior	CCO:MP0001436
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000885	ectopic Purkinje cell	CCO:MP0000885
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0001405	impaired coordination	CCO:MP0001405
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:88313	Ccnd1	"Ccnd1<tm1Phin>/Ccnd1<tm1Phin>,Tg(MMTV-Erbb2)NK1Mul/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:88313	Ccnd1	"Ccnd1<tm1Phin>/Ccnd1<tm1Phin>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0000854	abnormal cerebellum development	CCO:MP0000854
MGI:88313	Ccnd1	Ccnd1<tm1Phin>/Ccnd1<tm1Phin>	involves: 129S4/SvJae * C57BL/6	MP:0005551	abnormal eye electrophysiology	CCO:MP0005551
MGI:88313	Ccnd1	Ccnd1<tm1Phin>/Ccnd1<tm1Phin>	involves: 129S4/SvJae * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:88313	Ccnd1	Ccnd1<tm1Phin>/Ccnd1<tm1Phin>	involves: 129S4/SvJae * C57BL/6	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:88313	Ccnd1	Ccnd1<tm1Phin>/Ccnd1<tm1Phin>	involves: 129S4/SvJae * C57BL/6	MP:0001513	limb grasping	CCO:MP0001513
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88313	Ccnd1	Ccnd1<tm1(Ccnd2)Pisc>/Ccnd1<tm1(Ccnd2)Pisc>	involves: 129S4/SvJae	MP:0001513	limb grasping	CCO:MP0001513
MGI:88313	Ccnd1	Ccnd1<tm1(Ccnd2)Pisc>/Ccnd1<tm1(Ccnd2)Pisc>	involves: 129S4/SvJae	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0002679	abnormal corpus luteum	CCO:MP0002679
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001961	abnormal reflex	CCO:MP0001961
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001328	disorganized retinal layers	CCO:MP0001328
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006270	abnormal mammary gland growth during lactation	CCO:MP0006270
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0008507	thin retinal ganglion layer	CCO:MP0008507
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001385	pup cannibalization	CCO:MP0001385
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001260	increased body weight	CCO:MP0001260
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000120	malocclusion	CCO:MP0000120
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001148	enlarged testes	CCO:MP0001148
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:88313	Ccnd1	Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>	involves: 129S2/SvPas	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001328	disorganized retinal layers	CCO:MP0001328
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0008509	disorganized retinal ganglion layer	CCO:MP0008509
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Smarcb1<tm1Gvk>/Smarcb1<+>"	involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005358	abnormal incisor morphology	CCO:MP0005358
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002296	aspiration	CCO:MP0002296
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Smarcb1<tm1Gvk>/Smarcb1<+>"	involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Smarcb1<tm1Gvk>/Smarcb1<+>"	involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J	MP:0001265	decreased body size	CCO:MP0001265
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001513	limb grasping	CCO:MP0001513
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000458	abnormal mandible morphology	CCO:MP0000458
MGI:88313	Ccnd1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Smarcb1<tm1Gvk>/Smarcb1<+>"	involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J	MP:0003861	abnormal nervous system development	CCO:MP0003861
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001882	abnormal lactation	CCO:MP0001882
MGI:88313	Ccnd1	Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000455	abnormal maxilla morphology	CCO:MP0000455
MGI:88313	Ccnd1	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0000872	abnormal external granule cell layer morphology	CCO:MP0000872
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	MP:0001928	abnormal ovulation	CCO:MP0001928
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0008572	abnormal Purkinje cell dendrite morphology	CCO:MP0008572
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0000849	abnormal cerebellum morphology	CCO:MP0000849
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0000889	abnormal cerebellar molecular layer	CCO:MP0000889
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0000852	small cerebellum	CCO:MP0000852
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0000873	thin external granule cell layer	CCO:MP0000873
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	MP:0001926	female infertility	CCO:MP0001926
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:88314	Ccnd2	Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>	involves: 129S2/SvPas * C57BL/6J	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:88314	Ccnd2	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002811	macrocytic anemia	CCO:MP0002811
MGI:88314	Ccnd2	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002594	low mean erythrocyte cell number	CCO:MP0002594
MGI:88314	Ccnd2	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0000248	macrocytosis	CCO:MP0000248
MGI:88314	Ccnd2	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:88314	Ccnd2	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0001577	anemia	CCO:MP0001577
MGI:88314	Ccnd2	"Ccnd1<tm1Phin>/Ccnd1<tm1Phin>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0000854	abnormal cerebellum development	CCO:MP0000854
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0004808	abnormal hematopoietic stem cell morphology	CCO:MP0004808
MGI:88314	Ccnd2	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0000596	abnormal liver development	CCO:MP0000596
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:88314	Ccnd2	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:88314	Ccnd2	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000885	ectopic Purkinje cell	CCO:MP0000885
MGI:88314	Ccnd2	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000852	small cerebellum	CCO:MP0000852
MGI:88314	Ccnd2	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:88314	Ccnd2	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:88314	Ccnd2	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000875	abnormal cerebellar Purkinje cell layer	CCO:MP0000875
MGI:88314	Ccnd2	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88314	Ccnd2	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0001405	impaired coordination	CCO:MP0001405
MGI:88314	Ccnd2	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>"	Not Specified	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:88315	Ccnd3	"Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:88315	Ccnd3	"Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>,Rag2<tm1Fwa>/Rag2<tm1Fwa>"	involves: 129S/SvEv	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:88315	Ccnd3	"Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:88315	Ccnd3	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:88315	Ccnd3	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0004808	abnormal hematopoietic stem cell morphology	CCO:MP0004808
MGI:88315	Ccnd3	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002296	aspiration	CCO:MP0002296
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0001577	anemia	CCO:MP0001577
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88315	Ccnd3	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:88315	Ccnd3	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0001436	abnormal suckling behavior	CCO:MP0001436
MGI:88315	Ccnd3	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:88315	Ccnd3	Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>	Not Specified	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:88315	Ccnd3	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0000596	abnormal liver development	CCO:MP0000596
MGI:88315	Ccnd3	"Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>,Tg(Lck)4220Rmp/0"	involves: C57BL/6J * DBA/2	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:88315	Ccnd3	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0000248	macrocytosis	CCO:MP0000248
MGI:88315	Ccnd3	"Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>,Tg(Lck)4220Rmp/0"	involves: C57BL/6J * DBA/2	MP:0002083	premature death	CCO:MP0002083
MGI:88315	Ccnd3	Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>	Not Specified	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:88315	Ccnd3	Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>	Not Specified	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:88315	Ccnd3	"Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>,Tg(Lck)4220Rmp/0"	involves: C57BL/6J * DBA/2	MP:0003000	increased resistance to lymphoma	CCO:MP0003000
MGI:88315	Ccnd3	Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>	Not Specified	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:88315	Ccnd3	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:88315	Ccnd3	Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>	Not Specified	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:88315	Ccnd3	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88315	Ccnd3	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002811	macrocytic anemia	CCO:MP0002811
MGI:88315	Ccnd3	"Ccnd2<tm1Wbg>/Ccnd2<tm1Wbg>,Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>"	Not Specified	MP:0002594	low mean erythrocyte cell number	CCO:MP0002594
MGI:109595	Ccndbp1	Ccndbp1<tm1Drmr>/Ccndbp1<tm1Drmr>	involves: 129P2/OlaHsd * C57BL/6	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:109595	Ccndbp1	Ccndbp1<tm1Drmr>/Ccndbp1<tm1Drmr>	involves: 129P2/OlaHsd * C57BL/6	MP:0003324	liver adenoma	CCO:MP0003324
MGI:109595	Ccndbp1	Ccndbp1<tm1Drmr>/Ccndbp1<tm1Drmr>	involves: 129P2/OlaHsd * C57BL/6	MP:0005517	decreased liver regeneration	CCO:MP0005517
MGI:109595	Ccndbp1	Ccndbp1<tm1Drmr>/Ccndbp1<tm1Drmr>	involves: 129P2/OlaHsd * C57BL/6	MP:0004001	decreased hepatocyte proliferation	CCO:MP0004001
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0002397	abnormal bone marrow morphology	CCO:MP0002397
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0002124	abnormal red blood cell	CCO:MP0002124
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0002641	anisopoikilocytosis	CCO:MP0002641
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0000488	abnormal intestinal epithelium morphology	CCO:MP0000488
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0001577	anemia	CCO:MP0001577
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0002356	abnormal spleen red pulp morphology	CCO:MP0002356
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0001881	abnormal mammary gland physiology	CCO:MP0001881
MGI:88316	Ccne1	Ccne1<tm1Jro>/Ccne1<tm1Jro>	involves: 129/Sv * 129S4/SvJaeSor	MP:0001881	abnormal mammary gland physiology	CCO:MP0001881
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:88316	Ccne1	Ccne1<tm1Jro>/Ccne1<tm1Jro>	involves: 129/Sv * 129S4/SvJaeSor	MP:0000488	abnormal intestinal epithelium morphology	CCO:MP0000488
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0003135	increased erythroid progenitor cell number	CCO:MP0003135
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0008250	abnormal myeloid leukocyte morphology	CCO:MP0008250
MGI:88316	Ccne1	Ccne1<tm1Clur>/Ccne1<tm1Clur>	involves: 129/Sv	MP:0006271	abnormal involution of the mammary gland	CCO:MP0006271
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0002088	abnormal embryonic growth/weight/body size	CCO:MP0002088
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002977	abnormal patterning of the aortic arch	CCO:MP0002977
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0001622	abnormal vasculogenesis	CCO:MP0001622
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:88316	Ccne1	Ccne1<tm1Pisc>/Ccne1<tm1Pisc>	involves: 129S2/SvPas	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0005031	abnormal trophoblast layer morphology	CCO:MP0005031
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0001940	testicular hypoplasia	CCO:MP0001940
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<+>"	involves: 129S2/SvPas	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0000228	abnormal thrombopoiesis	CCO:MP0000228
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002127	abnormal cardiovascular system morphology	CCO:MP0002127
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:88316	Ccne1	"Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:88316	Ccne1	Ccne1<tm1Jro>/Ccne1<tm1Jro>	either: 129-Ccne1<tm1Jro> or B6.129-Ccne1<tm1Jro>	MP:0009336	increased splenocyte proliferation	CCO:MP0009336
MGI:88316	Ccne1	"Ccne1<tm1Jro>/?,Cdkn1a<tm1Led>/Cdkn1a<tm1Led>"	either: (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J) or (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6J)	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:88316	Ccne1	"Ccne1<tm1Jro>/?,Cdkn1a<tm1Led>/Cdkn1a<tm1Led>"	either: (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J) or (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6J)	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:88316	Ccne1	"Ccne1<tm1Jro>/?,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	either: (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6J) or (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * C57BL/6J)	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:88316	Ccne1	"Ccne1<tm1Jro>/?,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	either: (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6J) or (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * C57BL/6J)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:88316	Ccne1	"Ccne1<tm1Jro>/?,Kras<tm3Tyj>/?"	either: (involves: 129S2/SvPas * 129S4/SvJaeSor) or (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:88316	Ccne1	"Ccne1<tm1Jro>/?,Kras<tm3Tyj>/?"	either: (involves: 129S2/SvPas * 129S4/SvJaeSor) or (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6)	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:88316	Ccne1	"Ccne1<tm1Jro>/?,Cdkn1a<tm1Led>/Cdkn1a<tm1Led>"	either: (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J) or (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6J)	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:88316	Ccne1	Ccne1<tm1Jro>/Ccne1<tm1Jro>	either: 129-Ccne1<tm1Jro> or B6.129-Ccne1<tm1Jro>	MP:0004952	increased spleen weight	CCO:MP0004952
MGI:88316	Ccne1	Ccne1<tm1Jro>/Ccne1<tm1Jro>	either: 129-Ccne1<tm1Jro> or B6.129-Ccne1<tm1Jro>	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:88316	Ccne1	Ccne1<tm1Jro>/Ccne1<tm1Jro>	either: 129-Ccne1<tm1Jro> or B6.129-Ccne1<tm1Jro>	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0001622	abnormal vasculogenesis	CCO:MP0001622
MGI:1329034	Ccne2	Ccne2<tm1Boa>/Ccne2<tm1Boa>	involves: 129/Sv * C57BL/6	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0005031	abnormal trophoblast layer morphology	CCO:MP0005031
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0002088	abnormal embryonic growth/weight/body size	CCO:MP0002088
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:1329034	Ccne2	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1329034	Ccne2	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1329034	Ccne2	Ccne2<tm1Boa>/Ccne2<tm1Boa>	involves: 129/Sv * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1329034	Ccne2	Ccne2<tm1Boa>/Ccne2<tm1Boa>	involves: 129/Sv * C57BL/6	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:1329034	Ccne2	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	MP:0001925	male infertility	CCO:MP0001925
MGI:1329034	Ccne2	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	MP:0001147	small testis	CCO:MP0001147
MGI:1329034	Ccne2	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1329034	Ccne2	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1329034	Ccne2	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0001940	testicular hypoplasia	CCO:MP0001940
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<+>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:1329034	Ccne2	Ccne2<tm1Pisc>/Ccne2<tm1Pisc>	involves: 129S2/SvPas	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002127	abnormal cardiovascular system morphology	CCO:MP0002127
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0000228	abnormal thrombopoiesis	CCO:MP0000228
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:1329034	Ccne2	Ccne2<tm1Boa>/Ccne2<tm1Boa>	involves: 129/Sv * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<+>"	involves: 129S2/SvPas	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:1329034	Ccne2	Ccne2<tm1Boa>/Ccne2<tm1Boa>	involves: 129/Sv * C57BL/6	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002977	abnormal patterning of the aortic arch	CCO:MP0002977
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Pisc>/Ccne2<tm1Pisc>"	involves: 129S2/SvPas	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1329034	Ccne2	"Ccne1<tm1Pisc>/Ccne1<tm1Pisc>,Ccne2<tm1Boa>/Ccne2<tm1Boa>"	involves: 129/Sv * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003400	kinked neural tube	CCO:MP0003400
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001712	abnormal placenta development	CCO:MP0001712
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001719	absent vitelline blood vessels	CCO:MP0001719
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005650	abnormal limb bud morphology	CCO:MP0005650
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006108	abnormal hindbrain development	CCO:MP0006108
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003720	abnormal neural tube closure	CCO:MP0003720
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003864	abnormal midbrain development	CCO:MP0003864
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004076	abnormal vitelline vascular remodeling	CCO:MP0004076
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0009657	failure of chorioallantoic fusion	CCO:MP0009657
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003232	abnormal forebrain development	CCO:MP0003232
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001701	incomplete embryo turning	CCO:MP0001701
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001889	delayed brain development	CCO:MP0001889
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001723	disorganized vascular plexus	CCO:MP0001723
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005221	abnormal rostral-caudal axis patterning	CCO:MP0005221
MGI:102551	Ccnf	Ccnf<tm1.1Sje>/Ccnf<tm1.1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001726	abnormal allantois morphology	CCO:MP0001726
MGI:102890	Ccng1	Ccng1<tm1Sst>/Ccng1<tm1Sst>	involves: 129S/SvEv * C57BL/6	MP:0002658	abnormal liver regeneration	CCO:MP0002658
MGI:102890	Ccng1	Ccng1<tm1Sst>/Ccng1<tm1Sst>	involves: 129S/SvEv * C57BL/6	MP:0003402	decreased liver weight	CCO:MP0003402
MGI:102890	Ccng1	Ccng1<tm1Sst>/Ccng1<tm1Sst>	involves: 129S/SvEv * C57BL/6	MP:0002890	increased resistance to hepatoma	CCO:MP0002890
MGI:102890	Ccng1	Ccng1<tm1Noj>/Ccng1<tm1Noj>	involves: 129S2/SvPas * C57BL/6J	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:102890	Ccng1	Ccng1<tm1Noj>/Ccng1<tm1Noj>	involves: 129S2/SvPas * C57BL/6J	MP:0001658	increased mortality induced by gamma-irradiation	CCO:MP0001658
MGI:102890	Ccng1	Ccng1<tm1Noj>/Ccng1<tm1Noj>	involves: 129S2/SvPas * C57BL/6J	MP:0000511	abnormal intestinal mucosa morphology	CCO:MP0000511
MGI:102890	Ccng1	Ccng1<tm1Sst>/Ccng1<tm1Sst>	involves: 129S/SvEv * C57BL/6	MP:0002028	hepatoma	CCO:MP0002028
MGI:102890	Ccng1	Ccng1<tm1Sst>/Ccng1<tm1Sst>	involves: 129S/SvEv * C57BL/6	MP:0002053	decreased incidence of induced tumors	CCO:MP0002053
MGI:1341077	Ccni	Ccni<tm1Jro>/Ccni<tm1Jro>	involves: 129S4/SvJaeSor	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:1341077	Ccni	Ccni<tm1Jro>/Ccni<tm1Jro>	involves: 129S4/SvJaeSor	MP:0005160	proteinuria	CCO:MP0005160
MGI:1341077	Ccni	Ccni<tm1Jro>/Ccni<tm1Jro>	involves: 129S4/SvJaeSor	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1341077	Ccni	Ccni<tm1Jro>/Ccni<tm1Jro>	involves: 129S4/SvJaeSor	MP:0005264	glomerulosclerosis	CCO:MP0005264
MGI:1341077	Ccni	Ccni<tm1Jro>/Ccni<tm1Jro>	involves: 129S4/SvJaeSor	MP:0005553	increased circulating creatinine level	CCO:MP0005553
MGI:1341077	Ccni	Ccni<tm1Jro>/Ccni<tm1Jro>	involves: 129S4/SvJaeSor	MP:0005326	abnormal podocyte	CCO:MP0005326
MGI:1341077	Ccni	Ccni<tm1Jro>/Ccni<tm1Jro>	involves: 129S4/SvJaeSor	MP:0003606	kidney failure	CCO:MP0003606
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0000199	abnormal circulating serum albumin level	CCO:MP0000199
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005160	proteinuria	CCO:MP0005160
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005327	abnormal mesangial cell	CCO:MP0005327
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005326	abnormal podocyte	CCO:MP0005326
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005324	ascites	CCO:MP0005324
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005265	abnormal blood urea nitrogen level	CCO:MP0005265
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005328	abnormal circulating creatinine level	CCO:MP0005328
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0005264	glomerulosclerosis	CCO:MP0005264
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0002083	premature death	CCO:MP0002083
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0000274	enlarged heart	CCO:MP0000274
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0003643	spleen atrophy	CCO:MP0003643
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<tm1Shaw>	involves: 129X1/SvJ	MP:0003644	thymus atrophy	CCO:MP0003644
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<+>	Not Specified	MP:0005326	abnormal podocyte	CCO:MP0005326
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<+>	Not Specified	MP:0005165	increased susceptibility to injury	CCO:MP0005165
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<+>	Not Specified	MP:0005327	abnormal mesangial cell	CCO:MP0005327
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<+>	Not Specified	MP:0002136	abnormal kidney physiology	CCO:MP0002136
MGI:1330281	Cd2ap	Cd2ap<tm1Shaw>/Cd2ap<+>	Not Specified	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:1859866	Cdc20	Cdc20<Gt(XE368)Byg>/Cdc20<Gt(XE368)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1859866	Cdc20	"Cdc20<Gt(XE368)Byg>/Cdc20<Gt(XE368)Byg>,Pttg1<tm1Pzg>/Pttg1<tm1Pzg>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1859866	Cdc20	Cdc20<Gt(XE368)Byg>/Cdc20<Gt(XE368)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1859866	Cdc20	Cdc20<Gt(XE368)Byg>/Cdc20<Gt(XE368)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:1859866	Cdc20	"Cdc20<Gt(XE368)Byg>/Cdc20<Gt(XE368)Byg>,Pttg1<tm1Pzg>/Pttg1<tm1Pzg>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:103198	Cdc25a	Cdc25a<m1Rfp>/Cdc25a<m1Rfp>	multiple strains	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:103198	Cdc25a	"Cdc25a<tm1Kiyo>/Cdc25a<+>,Tg(MMTV-vHaras)SH1Led/?"	involves: 129/Sv * C57BL/6 * C57BL/6J * CD-1	MP:0002053	decreased incidence of induced tumors	CCO:MP0002053
MGI:103198	Cdc25a	Cdc25a<tm1Kiyo>/Cdc25a<tm1Kiyo>	involves: 129/Sv * C57BL/6	MP:0003693	abnormal embryo hatching	CCO:MP0003693
MGI:103198	Cdc25a	"Cdc25a<tm1Kiyo>/Cdc25a<+>,Tg(MMTV-Erbb2)NK1Mul/?"	involves: 129/Sv * C57BL/6 * FVB/N	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:103198	Cdc25a	Cdc25a<m1Rfp>/Cdc25a<m1Rfp>	multiple strains	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:103198	Cdc25a	Cdc25a<m1Rfp>/Cdc25a<m1Rfp>	multiple strains	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:103198	Cdc25a	Cdc25a<tm1Kiyo>/Cdc25a<tm1Kiyo>	involves: 129/Sv * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:103198	Cdc25a	Cdc25a<m1Rfp>/Cdc25a<m1Rfp>	multiple strains	MP:0005584	abnormal enzyme/coenzyme activity	CCO:MP0005584
MGI:103198	Cdc25a	"Cdc25a<tm1Kiyo>/Cdc25a<+>,Tg(MMTV-Erbb2)NK1Mul/?"	involves: 129/Sv * C57BL/6 * FVB/N	MP:0002053	decreased incidence of induced tumors	CCO:MP0002053
MGI:103198	Cdc25a	Cdc25a<tm1Dvb>/Cdc25a<tm1Dvb>	involves: 129/Sv	MP:0004500	increased incidence of ionizing radiation-induced tumors	CCO:MP0004500
MGI:103198	Cdc25a	Cdc25a<tm1Dvb>/Cdc25a<tm1Dvb>	involves: 129/Sv	MP:0004024	aneuploidy	CCO:MP0004024
MGI:103198	Cdc25a	Cdc25a<tm1Dvb>/Cdc25a<tm1Dvb>	involves: 129/Sv	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:103198	Cdc25a	Cdc25a<tm1Dvb>/Cdc25a<tm1Dvb>	involves: 129/Sv	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:103198	Cdc25a	Cdc25a<tm1.1Hpw>/Cdc25a<tm1.1Hpw>	involves: 129X1/SvJ * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:103198	Cdc25a	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0008108	abnormal small intestinal villus morphology	CCO:MP0008108
MGI:103198	Cdc25a	Cdc25a<tm1.1Hpw>/Cdc25a<tm1.1Hpw>	involves: 129X1/SvJ * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:103198	Cdc25a	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:103198	Cdc25a	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0001263	weight loss	CCO:MP0001263
MGI:103198	Cdc25a	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology	CCO:MP0004841
MGI:103198	Cdc25a	Cdc25a<tm1Hpw>/Cdc25a<tm1Hpw>	involves: 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:103198	Cdc25a	Cdc25a<tm1.1Hpw>/Cdc25a<tm1.1Hpw>	involves: 129X1/SvJ * C57BL/6	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:103198	Cdc25a	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:103198	Cdc25a	Cdc25a<tm1.1Hpw>/Cdc25a<tm1.1Hpw>	involves: 129X1/SvJ * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:103198	Cdc25a	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0008142	decreased small intestinal villus size	CCO:MP0008142
MGI:103198	Cdc25a	Cdc25a<Gt(OST186277)Lex>/Cdc25a<+>	involves: 129S5/SvEvBrd * C57BL/6J	MP:0000130	abnormal cancellous bone morphology	CCO:MP0000130
MGI:103198	Cdc25a	Cdc25a<Gt(OST186277)Lex>/Cdc25a<Gt(OST186277)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:99701	Cdc25b	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0001263	weight loss	CCO:MP0001263
MGI:99701	Cdc25b	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:99701	Cdc25b	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0008108	abnormal small intestinal villus morphology	CCO:MP0008108
MGI:99701	Cdc25b	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0008142	decreased small intestinal villus size	CCO:MP0008142
MGI:99701	Cdc25b	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:99701	Cdc25b	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology	CCO:MP0004841
MGI:99701	Cdc25b	Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>	Not Specified	MP:0001125	abnormal oocyte morphology	CCO:MP0001125
MGI:99701	Cdc25b	Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>	Not Specified	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:99701	Cdc25b	Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>	Not Specified	MP:0001919	abnormal reproductive system physiology	CCO:MP0001919
MGI:99701	Cdc25b	Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>	Not Specified	MP:0001926	female infertility	CCO:MP0001926
MGI:88350	Cdc25c	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0001263	weight loss	CCO:MP0001263
MGI:88350	Cdc25c	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:88350	Cdc25c	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology	CCO:MP0004841
MGI:88350	Cdc25c	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0008108	abnormal small intestinal villus morphology	CCO:MP0008108
MGI:88350	Cdc25c	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0008142	decreased small intestinal villus size	CCO:MP0008142
MGI:88350	Cdc25c	"Cdc25a<tm1Hpw>/Cdc25a<tm1.1Hpw>,Cdc25b<tm1Pjd>/Cdc25b<tm1Pjd>,Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>,Gt(ROSA)26Sor<tm1(cre/Esr1)Brn>/Gt(ROSA)26Sor<+>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:88350	Cdc25c	Cdc25c<tm1Hpw>/Cdc25c<tm1Hpw>	involves: 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:88351	Cdc2a	Cdc2a<Gt(P009F08)Bbd>/Cdc2a<Gt(pGT1-3)1Bbd>	involves: 129/Sv * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:88351	Cdc2a	Cdc2a<Gt(pGT1-3)1Bbd>/Cdc2a<Gt(pGT1-3)1Bbd>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:88351	Cdc2a	Cdc2a<Gt(P009F08)Bbd>/Cdc2a<Gt(P009F08)Bbd>	involves: 129/Sv * 129X1/SvJ * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001147	small testis	CCO:MP0001147
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001127	small ovary	CCO:MP0001127
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001924	infertility	CCO:MP0001924
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:88351	Cdc2a	Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>	involves: C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:88351	Cdc2a	Cdc2a<tm1(Cdk2)Kald>/Cdc2a<tm1(Cdk2)Kald>	Not Specified	MP:0008527	embryonic lethality at implantation	CCO:MP0008527
MGI:88351	Cdc2a	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0004805	absent oocytes	CCO:MP0004805
MGI:88353	Cdc2l1	Cdc2l1<Gt(XG836)Byg>/Cdc2l1<Gt(XG836)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002051	skin papilloma	CCO:MP0002051
MGI:88353	Cdc2l1	Cdc2l1<Gt(XG836)Byg>/Cdc2l1<Gt(XG836)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001219	thickened epidermis	CCO:MP0001219
MGI:88353	Cdc2l1	Cdc2l1<Gt(XG836)Byg>/Cdc2l1<Gt(XG836)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:88353	Cdc2l1	Cdc2l1<tm1Vjk>/Cdc2l1<tm1Vjk>	involves: 129S/SvEv * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:88353	Cdc2l1	Cdc2l1<tm1Vjk>/Cdc2l1<tm1Vjk>	involves: 129S/SvEv * C57BL/6	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:88353	Cdc2l1	Cdc2l1<tm1Vjk>/Cdc2l1<tm1Vjk>	involves: 129S/SvEv * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:88353	Cdc2l1	Cdc2l1<tm1Vjk>/Cdc2l1<tm1Vjk>	involves: 129S/SvEv * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:88353	Cdc2l1	Cdc2l1<tm1Vjk>/Cdc2l1<tm1Vjk>	involves: 129S/SvEv * C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0001240	abnormal epidermis stratum corneum morphology	CCO:MP0001240
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0000375	abnormal hair follicle structure	CCO:MP0000375
MGI:106211	Cdc42	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0001247	dermal cysts	CCO:MP0001247
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0002655	abnormal keratinocyte morphology	CCO:MP0002655
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0000388	absent inner root sheath	CCO:MP0000388
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0001242	hyperkeratosis	CCO:MP0001242
MGI:106211	Cdc42	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0001222	epidermal hyperplasia	CCO:MP0001222
MGI:106211	Cdc42	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0000935	abnormal folding of telencephalic vesicles	CCO:MP0000935
MGI:106211	Cdc42	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0000936	small telencephalic vesicles	CCO:MP0000936
MGI:106211	Cdc42	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0005157	holoprosencephaly	CCO:MP0005157
MGI:106211	Cdc42	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0004261	abnormal embryonic neuroepithelium morphology	CCO:MP0004261
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:106211	Cdc42	Cdc42<tm1Brak>/Cdc42<tm1Brak>	Not Specified	MP:0000386	abnormal hair follicle root sheath	CCO:MP0000386
MGI:106211	Cdc42	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:106211	Cdc42	Cdc42<tm1Fwa>/Cdc42<tm1Fwa>	involves: 129S6/SvEvTac	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:106211	Cdc42	Cdc42<tm1Fwa>/Cdc42<tm1Fwa>	involves: 129S6/SvEvTac	MP:0001675	abnormal ectoderm development	CCO:MP0001675
MGI:106211	Cdc42	Cdc42<tm1Fwa>/Cdc42<tm1Fwa>	involves: 129S6/SvEvTac	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:106211	Cdc42	Cdc42<tm1Fwa>/Cdc42<tm1Fwa>	involves: 129S6/SvEvTac	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:106211	Cdc42	Cdc42<tm1Fwa>/Cdc42<tm1Fwa>	involves: 129S6/SvEvTac	MP:0003988	disorganized embryonic tissue	CCO:MP0003988
MGI:106211	Cdc42	Cdc42<Gt(Ex160)Byg>/Cdc42<Gt(Ex160)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1338073	Cdc45l	Cdc45l<tm1Dta>/Cdc45l<tm1Dta>	involves: 129S4/SvJae * C57BL/6	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:1338073	Cdc45l	Cdc45l<tm1Dta>/Cdc45l<+>	involves: 129S4/SvJae * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1338073	Cdc45l	Cdc45l<tm1Dta>/Cdc45l<tm1Dta>	involves: 129S4/SvJae * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/Tg(EF1A-Cdc7)DKO28Hmas"	involves: C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Trp53<tm1.1Mok>/Trp53<tm1.1Mok>"	involves: 129S/SvEv * C57BL/6	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0008057	abnormal DNA replication	CCO:MP0008057
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0001127	small ovary	CCO:MP0001127
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0003051	curly tail	CCO:MP0003051
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Tg(EF1A-Cdc7)DKO28Hmas/0"	involves: C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:1309511	Cdc7	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Trp53<tm1.1Mok>/Trp53<tm1.1Mok>"	involves: 129S/SvEv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1309511	Cdc7	Cdc7<tm1Hmas>/Cdc7<tm1Hmas>	involves: C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0000462	abnormal digestive system morphology	CCO:MP0000462
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0002989	small kidney	CCO:MP0002989
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001402	hypoactivity	CCO:MP0001402
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001157	small seminal gland	CCO:MP0001157
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001147	small testis	CCO:MP0001147
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0002188	small heart	CCO:MP0002188
MGI:2384876	Cdc73	Cdc73<Gt(RRE190)Byg>/Cdc73<Gt(RRE190)Byg>	involves: 129P2/OlaHsd	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0002691	small stomach	CCO:MP0002691
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001961	abnormal reflex	CCO:MP0001961
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0005574	decreased breathing frequency	CCO:MP0005574
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001654	hepatic necrosis	CCO:MP0001654
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0003641	small lung	CCO:MP0003641
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0003861	abnormal nervous system development	CCO:MP0003861
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0003946	renal necrosis	CCO:MP0003946
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0004819	decreased skeletal muscle mass	CCO:MP0004819
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0008844	decreased subcutaneous adipose tissue amount	CCO:MP0008844
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0008853	decreased abdominal adipose tissue amount	CCO:MP0008853
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0005324	ascites	CCO:MP0005324
MGI:2384876	Cdc73	Cdc73<tm1.1Btt>/Cdc73<tm1.1Btt>	involves: 129S4/SvJae * BALB/cJ	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0000692	small spleen	CCO:MP0000692
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001263	weight loss	CCO:MP0001263
MGI:2384876	Cdc73	Cdc73<Gt(RRE190)Byg>/Cdc73<Gt(RRE190)Byg>	involves: 129P2/OlaHsd	MP:0001728	failure of embryo implantation	CCO:MP0001728
MGI:2384876	Cdc73	Cdc73<Gt(RRE190)Byg>/Cdc73<Gt(RRE190)Byg>	involves: 129P2/OlaHsd	MP:0005028	abnormal trophectoderm morphology	CCO:MP0005028
MGI:2384876	Cdc73	Cdc73<Gt(RRE190)Byg>/Cdc73<Gt(RRE190)Byg>	involves: 129P2/OlaHsd	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0002164	abnormal gland physiology	CCO:MP0002164
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0000601	small liver	CCO:MP0000601
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0000618	small salivary gland	CCO:MP0000618
MGI:2384876	Cdc73	"Cdc73<tm1Btt>/Cdc73<tm1Btt>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1196274	Cdca8	Cdca8<tm1Tatn>/Cdca8<tm1Tatn>	involves: C57BL/6 * CBA	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1196274	Cdca8	Cdca8<tm1Tatn>/Cdca8<tm1Tatn>	involves: C57BL/6 * CBA	MP:0003707	increased nucleus count	CCO:MP0003707
MGI:1196274	Cdca8	Cdca8<tm1Tatn>/Cdca8<tm1Tatn>	involves: C57BL/6 * CBA	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1196274	Cdca8	Cdca8<tm1Tatn>/Cdca8<tm1Tatn>	involves: C57BL/6 * CBA	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1196274	Cdca8	Cdca8<tm1Tatn>/Cdca8<tm1Tatn>	involves: C57BL/6 * CBA	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1196274	Cdca8	"Cdca8<tm1Tatn>/Cdca8<tm1Tatn>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL/6 * CBA	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1196274	Cdca8	Cdca8<tm1Tatn>/Cdca8<tm1Tatn>	involves: C57BL/6 * CBA	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0003567	abnormal fetal cardiomyocyte proliferation	CCO:MP0003567
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0004808	abnormal hematopoietic stem cell morphology	CCO:MP0004808
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0003105	abnormal heart atrium morphology	CCO:MP0003105
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>"	involves: 129S1/Sv * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>"	involves: 129S1/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004567	decreased myocardial fiber number	CCO:MP0004567
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0002188	small heart	CCO:MP0002188
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0001262	decreased body weight	CCO:MP0001262
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000278	abnormal myocardial fiber morphology	CCO:MP0000278
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0000609	abnormal liver physiology	CCO:MP0000609
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000285	abnormal cardiac valve morphology	CCO:MP0000285
MGI:104772	Cdk2	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0001627	abnormal cardiac output	CCO:MP0001627
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv	MP:0004001	decreased hepatocyte proliferation	CCO:MP0004001
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001147	small testis	CCO:MP0001147
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001127	small ovary	CCO:MP0001127
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001924	infertility	CCO:MP0001924
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0004805	absent oocytes	CCO:MP0004805
MGI:104772	Cdk2	"Cdc2a<tm1(Cdk2)Kald>/Cdc2a<+>,Cdk2<tm1Kald>/Cdk2<tm1Kald>"	involves: 129S1/Sv	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv	MP:0001924	infertility	CCO:MP0001924
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0006138	congestive heart failure	CCO:MP0006138
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0003567	abnormal fetal cardiomyocyte proliferation	CCO:MP0003567
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0004564	enlarged myocardial fiber	CCO:MP0004564
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<+>,Cdk4<tm2.1Bbd>/Cdk4<+>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:104772	Cdk2	"Cdk2<tm2Sgo>/Cdk2<tm2Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>,Tg(CMV-cre/ESR1)1Ipc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0001265	decreased body size	CCO:MP0001265
MGI:104772	Cdk2	"Cdk2<tm2Sgo>/Cdk2<tm2Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>,Tg(CMV-cre/ESR1)1Ipc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0004803	increased susceptibility to autoimmune diabetes	CCO:MP0004803
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0001924	infertility	CCO:MP0001924
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0001930	abnormal meiosis	CCO:MP0001930
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0001125	abnormal oocyte morphology	CCO:MP0001125
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0001932	abnormal spermiogenesis	CCO:MP0001932
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0004833	ovary atrophy	CCO:MP0004833
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0004894	uterus atrophy	CCO:MP0004894
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0004833	ovary atrophy	CCO:MP0004833
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0001931	abnormal oogenesis	CCO:MP0001931
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0004805	absent oocytes	CCO:MP0004805
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:104772	Cdk2	Cdk2<tm1Sgo>/Cdk2<tm1Sgo>	involves: 129/Sv * CD-1	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:104772	Cdk2	Cdk2<tm1Kald>/Cdk2<tm1Kald>	involves: 129S1/Sv * C57BL/6	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001931	abnormal oogenesis	CCO:MP0001931
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:104772	Cdk2	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001924	infertility	CCO:MP0001924
MGI:1202069	Cdk2ap1	Cdk2ap1<tm1Dtw>/Cdk2ap1<tm1Dtw>	involves: 129S4/SvJae	MP:0000445	short snout	CCO:MP0000445
MGI:1202069	Cdk2ap1	Cdk2ap1<tm1Dtw>/Cdk2ap1<tm1Dtw>	involves: 129S4/SvJae	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1202069	Cdk2ap1	Cdk2ap1<tm1Dtw>/Cdk2ap1<tm1Dtw>	involves: 129S4/SvJae	MP:0003743	abnormal facial morphology	CCO:MP0003743
MGI:1202069	Cdk2ap1	Cdk2ap1<tm1Dtw>/Cdk2ap1<tm1Dtw>	involves: 129S4/SvJae	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1202069	Cdk2ap1	Cdk2ap1<tm1Dtw>/Cdk2ap1<+>	involves: 129S4/SvJae	MP:0000445	short snout	CCO:MP0000445
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:88357	Cdk4	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0008365	adenohypophysis hypoplasia	CCO:MP0008365
MGI:88357	Cdk4	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:88357	Cdk4	"Cdk4<tm1Kiyo>/Cdk4<+>,Lin9<tm1Orc>/Lin9<+>"	involves: 129S1/Sv	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0000609	abnormal liver physiology	CCO:MP0000609
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	MP:0001926	female infertility	CCO:MP0001926
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004567	decreased myocardial fiber number	CCO:MP0004567
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	MP:0001925	male infertility	CCO:MP0001925
MGI:88357	Cdk4	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0001925	male infertility	CCO:MP0001925
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	MP:0002785	absent Leydig cells	CCO:MP0002785
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	MP:0005159	azoospermia	CCO:MP0005159
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	MP:0008332	decreased lactotroph cell number	CCO:MP0008332
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv	MP:0008365	adenohypophysis hypoplasia	CCO:MP0008365
MGI:88357	Cdk4	"Cdk4<tm1Kiyo>/Cdk4<+>,Lin9<tm1Orc>/Lin9<+>"	involves: 129S1/Sv	MP:0004804	decreased susceptibility to autoimmune diabetes	CCO:MP0004804
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000285	abnormal cardiac valve morphology	CCO:MP0000285
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0002188	small heart	CCO:MP0002188
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0003105	abnormal heart atrium morphology	CCO:MP0003105
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000278	abnormal myocardial fiber morphology	CCO:MP0000278
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0003567	abnormal fetal cardiomyocyte proliferation	CCO:MP0003567
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0004808	abnormal hematopoietic stem cell morphology	CCO:MP0004808
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>"	involves: 129S1/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:88357	Cdk4	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0001926	female infertility	CCO:MP0001926
MGI:88357	Cdk4	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>"	involves: 129S1/Sv * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88357	Cdk4	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>"	involves: 129S1/Sv * C57BL/6	MP:0001627	abnormal cardiac output	CCO:MP0001627
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0003567	abnormal fetal cardiomyocyte proliferation	CCO:MP0003567
MGI:88357	Cdk4	"Cdk2<tm2Sgo>/Cdk2<tm2Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>,Tg(CMV-cre/ESR1)1Ipc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0004803	increased susceptibility to autoimmune diabetes	CCO:MP0004803
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<+>,Cdk4<tm2.1Bbd>/Cdk4<+>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0004564	enlarged myocardial fiber	CCO:MP0004564
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:88357	Cdk4	"Cdk2<tm2Sgo>/Cdk2<tm2Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>,Tg(CMV-cre/ESR1)1Ipc/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0001265	decreased body size	CCO:MP0001265
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:88357	Cdk4	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm2.1Bbd>/Cdk4<tm2.1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL	MP:0006138	congestive heart failure	CCO:MP0006138
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001762	polyuria	CCO:MP0001762
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001759	increased urine glucose level	CCO:MP0001759
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001759	increased urine glucose level	CCO:MP0001759
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002679	abnormal corpus luteum	CCO:MP0002679
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002784	abnormal Sertoli cell morphology	CCO:MP0002784
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0009172	small pancreatic islets	CCO:MP0009172
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0003698	abnormal male reproductive system physiology	CCO:MP0003698
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002727	decreased circulating insulin level	CCO:MP0002727
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001265	decreased body size	CCO:MP0001265
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0003356	impaired luteinization	CCO:MP0003356
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:88357	Cdk4	Cdk4<tm1.1Bbd>/Cdk4<+>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0003645	increased pancreatic beta cell number	CCO:MP0003645
MGI:88357	Cdk4	Cdk4<tm1.1Bbd>/Cdk4<tm1.1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0003645	increased pancreatic beta cell number	CCO:MP0003645
MGI:88357	Cdk4	Cdk4<tm1.1Bbd>/Cdk4<tm1.1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001152	Leydig cell hyperplasia	CCO:MP0001152
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0009008	delayed estrous cycle	CCO:MP0009008
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0002679	abnormal corpus luteum	CCO:MP0002679
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0003699	abnormal female reproductive system physiology	CCO:MP0003699
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0005536	Leydig cell hypoplasia	CCO:MP0005536
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002893	ketoaciduria	CCO:MP0002893
MGI:88357	Cdk4	Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>	involves: 129S1/Sv * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0005185	decreased circulating progesterone level	CCO:MP0005185
MGI:88357	Cdk4	Cdk4<tm1.1Bbd>/Cdk4<tm1.1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001260	increased body weight	CCO:MP0001260
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001392	abnormal locomotor activity	CCO:MP0001392
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001926	female infertility	CCO:MP0001926
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001559	hyperglycemia	CCO:MP0001559
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001262	decreased body weight	CCO:MP0001262
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001426	polydipsia	CCO:MP0001426
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002790	decreased circulating follicle stimulating hormone level	CCO:MP0002790
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001399	hyperactivity	CCO:MP0001399
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001524	impaired limb coordination	CCO:MP0001524
MGI:88357	Cdk4	Cdk4<tm1Bbd>/Cdk4<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0001127	small ovary	CCO:MP0001127
MGI:88357	Cdk4	"Cdk4<tm1.1Bbd>/Cdk4<+>,Kras<tm1Bbd>/Kras<+>,Tg(CMV-cre)1Cgn/?"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:88357	Cdk4	"Cdk4<tm1.1Bbd>/Cdk4<+>,Kras<tm1Bbd>/Kras<+>,Tg(CMV-cre)1Cgn/?"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:88357	Cdk4	"Cdk4<tm1.1Bbd>/Cdk4<+>,Kras<tm1Bbd>/Kras<+>,Tg(CMV-cre)1Cgn/?"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0002014	papilloma	CCO:MP0002014
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0002124	abnormal red blood cell	CCO:MP0002124
MGI:88357	Cdk4	"Cdk4<tm1.1Bbd>/Cdk4<+>,Kras<tm1Bbd>/Kras<+>,Tg(CMV-cre)1Cgn/?"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:88357	Cdk4	"Cdk4<tm1.1Bbd>/Cdk4<+>,Kras<tm1Bbd>/Kras<+>,Tg(CMV-cre)1Cgn/?"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:88357	Cdk4	"Cdk4<tm1.1Bbd>/Cdk4<+>,Kras<tm1Bbd>/Kras<+>,Tg(CMV-cre)1Cgn/?"	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0009143	abnormal pancreatic duct morphology	CCO:MP0009143
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:88357	Cdk4	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:101765	Cdk5	"Cdk5<tm1Bibb>/Cdk5<tm1Bibb>,Tg(Prnp-cre/Esr1)28.4Ics/0"	Not Specified	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:101765	Cdk5	"Cdk5<tm1Bibb>/Cdk5<tm1Bibb>,Tg(Prnp-cre/Esr1)28.4Ics/0"	Not Specified	MP:0004859	abnormal synaptic plasticity	CCO:MP0004859
MGI:101765	Cdk5	"Cdk5<tm1Bibb>/Cdk5<tm1Bibb>,Tg(Prnp-cre/Esr1)28.4Ics/0"	Not Specified	MP:0002923	increased post-tetanic potential	CCO:MP0002923
MGI:101765	Cdk5	"Cdk5<tm1Bibb>/Cdk5<tm1Bibb>,Tg(Prnp-cre/Esr1)28.4Ics/0"	Not Specified	MP:0002912	abnormal excitatory postsynaptic potential	CCO:MP0002912
MGI:101765	Cdk5	"Cdk5<tm1Bibb>/Cdk5<tm1Bibb>,Tg(Prnp-cre/Esr1)28.4Ics/0"	Not Specified	MP:0002207	abnormal long term potentiation	CCO:MP0002207
MGI:101765	Cdk5	"Cdk5<tm1Bibb>/Cdk5<tm1Bibb>,Tg(Prnp-cre/Esr1)28.4Ics/0"	Not Specified	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:101765	Cdk5	"Cdk5<tm1Bibb>/Cdk5<tm1Bibb>,Tg(Prnp-cre/Esr1)28.4Ics/0"	Not Specified	MP:0002910	abnormal excitatory postsynaptic currents	CCO:MP0002910
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0001071	abnormal facial nerve morphology	CCO:MP0001071
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0004097	abnormal cerebellar cortex morphology	CCO:MP0004097
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0000790	abnormal stratification in cerebral cortex	CCO:MP0000790
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0000812	abnormal dentate gyrus morphology	CCO:MP0000812
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0000813	abnormal hippocampal laminar structure	CCO:MP0000813
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0002739	abnormal olfactory bulb development	CCO:MP0002739
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0005112	abnormal spinal cord ventral horn morphology	CCO:MP0005112
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0002883	chromatolysis	CCO:MP0002883
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0008439	abnormal cortical plate morphology	CCO:MP0008439
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0001076	abnormal hypoglossal nerve morphology	CCO:MP0001076
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0001575	cyanosis	CCO:MP0001575
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0000937	abnormal motor neuron morphology	CCO:MP0000937
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0001435	no suckling reflex	CCO:MP0001435
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0000746	weakness	CCO:MP0000746
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0001491	unresponsive to tactile stimuli	CCO:MP0001491
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0001392	abnormal locomotor activity	CCO:MP0001392
MGI:101765	Cdk5	Cdk5<tm1Kul>/Cdk5<tm1Kul>	involves: 129S4/SvJae * C57BL/6	MP:0001956	hypopnea	CCO:MP0001956
MGI:101765	Cdk5	"Cdk5<tm2Kul>/Cdk5<tm2Kul>,Tg(Nefh-cre)12Kul/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	MP:0000808	abnormal hippocampus development	CCO:MP0000808
MGI:101765	Cdk5	Cdk5<tm2Kul>/Cdk5<tm2Kul>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:101765	Cdk5	"Cdk5<tm2Kul>/Cdk5<tm2Kul>,Tg(Nefh-cre)12Kul/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	MP:0000854	abnormal cerebellum development	CCO:MP0000854
MGI:101765	Cdk5	"Cdk5<tm2Kul>/Cdk5<tm2Kul>,Tg(Nefh-cre)12Kul/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	MP:0002739	abnormal olfactory bulb development	CCO:MP0002739
MGI:101765	Cdk5	"Cdk5<tm2Kul>/Cdk5<tm2Kul>,Tg(Nefh-cre)12Kul/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N	MP:0000913	abnormal brain development	CCO:MP0000913
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004567	decreased myocardial fiber number	CCO:MP0004567
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0009542	decreased thymocyte apoptosis	CCO:MP0009542
MGI:1277162	Cdk6	"Cdk6<tm1Phin>/Cdk6<tm1Phin>,Tg(Lck-Akt1*E40K)E-3Pnt/0"	involves: 129S4/SvJae	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:1277162	Cdk6	"Cdk6<tm1Phin>/Cdk6<+>,Tg(Lck-Akt1*E40K)E-3Pnt/0"	involves: 129S4/SvJae	MP:0002083	premature death	CCO:MP0002083
MGI:1277162	Cdk6	"Cdk6<tm1Phin>/Cdk6<+>,Tg(Lck-Akt1*E40K)E-3Pnt/0"	involves: 129S4/SvJae	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0003850	abnormal thymocyte activation	CCO:MP0003850
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0003644	thymus atrophy	CCO:MP0003644
MGI:1277162	Cdk6	Cdk6<tm1Phin>/Cdk6<tm1Phin>	involves: 129S4/SvJae	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0005641	increased mean corpuscular hemoglobin concentration	CCO:MP0005641
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002682	decreased mature ovarian follicle number	CCO:MP0002682
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0008082	increased single-positive T cell number	CCO:MP0008082
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002396	abnormal hematopoietic system morphology/development	CCO:MP0002396
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002590	increased mean corpuscular volume	CCO:MP0002590
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001924	infertility	CCO:MP0001924
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1277162	Cdk6	"Cdk2<tm1Sgo>/Cdk2<tm1Sgo>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001931	abnormal oogenesis	CCO:MP0001931
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0003644	thymus atrophy	CCO:MP0003644
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0008255	decreased megakaryocyte cell number	CCO:MP0008255
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0002124	abnormal red blood cell	CCO:MP0002124
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:1277162	Cdk6	"Cdk4<tm1Bbd>/Cdk4<tm1Bbd>,Cdk6<tm1Bbd>/Cdk6<tm1Bbd>"	involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000694	spleen hypoplasia	CCO:MP0000694
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002124	abnormal red blood cell	CCO:MP0002124
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000703	abnormal thymus morphology	CCO:MP0000703
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000692	small spleen	CCO:MP0000692
MGI:1277162	Cdk6	Cdk6<tm1Bbd>/Cdk6<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002356	abnormal spleen red pulp morphology	CCO:MP0002356
MGI:104556	Cdkn1a	"Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Tg(MMTV-vHaras)SH1Led/0"	involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000526	small inner medullary pyramid	CCO:MP0000526
MGI:104556	Cdkn1a	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004320	split sternum	CCO:MP0004320
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004174	abnormal spine curvature	CCO:MP0004174
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004002	abnormal jejunum morphology	CCO:MP0004002
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0003613	abnormal kidney medulla development	CCO:MP0003613
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0008148	abnormal rib-sternum attachment	CCO:MP0008148
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0003052	omphalocele	CCO:MP0003052
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0009399	increased skeletal muscle fiber size	CCO:MP0009399
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002267	abnormal bronchiole morphology	CCO:MP0002267
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000761	thin diaphragm muscle	CCO:MP0000761
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004819	decreased skeletal muscle mass	CCO:MP0004819
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002581	abnormal ileum morphology	CCO:MP0002581
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0003237	abnormal lens epithelium morphology	CCO:MP0003237
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104556	Cdkn1a	"Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Wap-cre)1Gsc/0"	involves: 129S2/SvPas * C57BL/6 * FVB/N	MP:0006270	abnormal mammary gland growth during lactation	CCO:MP0006270
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:104556	Cdkn1a	"Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Tg(MMTV-vHaras)SH1Led/0"	involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N	MP:0000621	salivary adenocarcinoma	CCO:MP0000621
MGI:104556	Cdkn1a	"Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Tg(MMTV-vHaras)SH1Led/0"	involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104556	Cdkn1a	"Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Tg(MMTV-vHaras)SH1Led/0"	involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004321	short sternum	CCO:MP0004321
MGI:104556	Cdkn1a	"Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Tg(MMTV-vHaras)SH1Led/0"	involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N	MP:0005248	abnormal Harderian gland morphology	CCO:MP0005248
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000757	herniated abdominal wall	CCO:MP0000757
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000157	abnormal sternum morphology	CCO:MP0000157
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000131	abnormal long bone epiphysis morphology	CCO:MP0000131
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002270	abnormal respiratory alveoli morphology	CCO:MP0002270
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002264	abnormal bronchus morphology	CCO:MP0002264
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000153	rib bifurcation	CCO:MP0000153
MGI:104556	Cdkn1a	"Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Tg(MMTV-vHaras)SH1Led/0"	involves: 129S2/SvPas * C57BL/6J * CD-1 * FVB/N	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0004796	increased anti-histone antibody level	CCO:MP0004796
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0004771	increased anti-single stranded DNA antibody level	CCO:MP0004771
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0008499	increased IgG1 level	CCO:MP0008499
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<+>	involves: 129S6/SvEvTac	MP:0008538	decreased zigzag hair amount	CCO:MP0008538
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<+>	involves: 129S6/SvEvTac	MP:0000400	abnormal awl hair	CCO:MP0000400
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<+>	involves: 129S6/SvEvTac	MP:0000405	abnormal auchene hairs	CCO:MP0000405
MGI:104556	Cdkn1a	"Brca1<tm2Mak>/Brca1<tm2Mak>,Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:104556	Cdkn1a	Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>	involves: 129S2/SvPas	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Wrn<tm1Led>/Wrn<tm1Led>"	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0008538	decreased zigzag hair amount	CCO:MP0008538
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0004796	increased anti-histone antibody level	CCO:MP0004796
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0004771	increased anti-single stranded DNA antibody level	CCO:MP0004771
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0000400	abnormal awl hair	CCO:MP0000400
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0000405	abnormal auchene hairs	CCO:MP0000405
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0002083	premature death	CCO:MP0002083
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Hus1<tm1Led>/Hus1<tm1Led>"	involves: 129S6/SvEvTac	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005327	abnormal mesangial cell	CCO:MP0005327
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	involves: 129S6/SvEvTac	MP:0003725	increased autoantibody level	CCO:MP0003725
MGI:104556	Cdkn1a	"Ccne1<tm1Jro>/?,Cdkn1a<tm1Led>/Cdkn1a<tm1Led>"	either: (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J) or (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6J)	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Fgfr3<tm1Cxd>/Fgfr3<tm1Cxd>"	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0003055	abnormal long bone epiphyseal plate morphology	CCO:MP0003055
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Fgfr3<tm1Cxd>/Fgfr3<tm1Cxd>"	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0005508	abnormal skeleton morphology	CCO:MP0005508
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Fgfr3<tm1Cxd>/Fgfr3<tm1Cxd>"	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0002427	disproportionate dwarf	CCO:MP0002427
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0003725	increased autoantibody level	CCO:MP0003725
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Hus1<tm1Led>/Hus1<tm1Led>"	involves: 129S6/SvEvTac	MP:0008410	increased cellular sensitivity to ultraviolet irradiation	CCO:MP0008410
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Hus1<tm1Led>/Hus1<tm1Led>"	involves: 129S6/SvEvTac	MP:0008409	increased cellular sensitivity to hydroxyurea	CCO:MP0008409
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002607	decreased basophil cell number	CCO:MP0002607
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	NIH.Cg-Cdkn1a<tm1Led>	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:104556	Cdkn1a	"Ccne1<tm1Jro>/?,Cdkn1a<tm1Led>/Cdkn1a<tm1Led>"	either: (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J) or (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6J)	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:104556	Cdkn1a	"Ccne1<tm1Jro>/?,Cdkn1a<tm1Led>/Cdkn1a<tm1Led>"	either: (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J) or (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6J)	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005012	decreased eosinophil cell number	CCO:MP0005012
MGI:104556	Cdkn1a	Cdkn1a<tm1(HBsAg)Xya>/Cdkn1a<tm1(HBsAg)Xya>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002038	carcinoma	CCO:MP0002038
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002494	increased IgM level	CCO:MP0002494
MGI:104556	Cdkn1a	Cdkn1a<tm1Led>/Cdkn1a<tm1Led>	NIH.Cg-Cdkn1a<tm1Led>	MP:0003000	increased resistance to lymphoma	CCO:MP0003000
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0001828	abnormal T cell activation	CCO:MP0001828
MGI:104556	Cdkn1a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005160	proteinuria	CCO:MP0005160
MGI:104556	Cdkn1a	Cdkn1a<tm1(HBsAg)Xya>/Cdkn1a<tm1(HBsAg)Xya>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:104556	Cdkn1a	Cdkn1a<tm1(HBsAg)Xya>/Cdkn1a<tm1(HBsAg)Xya>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002018	malignant tumors	CCO:MP0002018
MGI:104556	Cdkn1a	Cdkn1a<tm1(HBsAg)Xya>/Cdkn1a<tm1(HBsAg)Xya>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:104556	Cdkn1a	Cdkn1a<tm2(HBx)Xya>/Cdkn1a<+>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:104556	Cdkn1a	Cdkn1a<tm2(HBx)Xya>/Cdkn1a<tm2(HBx)Xya>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002038	carcinoma	CCO:MP0002038
MGI:104556	Cdkn1a	Cdkn1a<tm2(HBx)Xya>/Cdkn1a<tm2(HBx)Xya>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002018	malignant tumors	CCO:MP0002018
MGI:104556	Cdkn1a	Cdkn1a<tm2(HBx)Xya>/Cdkn1a<tm2(HBx)Xya>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:104556	Cdkn1a	Cdkn1a<tm2(HBx)Xya>/Cdkn1a<tm2(HBx)Xya>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:104556	Cdkn1a	Cdkn1a<tm1(HBsAg)Xya>/Cdkn1a<+>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002038	carcinoma	CCO:MP0002038
MGI:104556	Cdkn1a	Cdkn1a<tm1(HBsAg)Xya>/Cdkn1a<+>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002018	malignant tumors	CCO:MP0002018
MGI:104556	Cdkn1a	Cdkn1a<tm1(HBsAg)Xya>/Cdkn1a<+>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:104556	Cdkn1a	Cdkn1a<tm1(HBsAg)Xya>/Cdkn1a<+>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:104556	Cdkn1a	Cdkn1a<tm2(HBx)Xya>/Cdkn1a<+>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:104556	Cdkn1a	Cdkn1a<tm2(HBx)Xya>/Cdkn1a<+>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002018	malignant tumors	CCO:MP0002018
MGI:104556	Cdkn1a	Cdkn1a<tm2(HBx)Xya>/Cdkn1a<+>	either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0002038	carcinoma	CCO:MP0002038
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000636	enlarged pituitary gland	CCO:MP0000636
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000642	enlarged adrenal glands	CCO:MP0000642
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0001429	dehydration	CCO:MP0001429
MGI:104565	Cdkn1b	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>"	involves: 129S1/Sv * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0002083	premature death	CCO:MP0002083
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0003825	abnormal pillar cell morphology	CCO:MP0003825
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0004498	increased supporting cell number	CCO:MP0004498
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0004407	increased cochlear hair cell number	CCO:MP0004407
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0001264	increased body size	CCO:MP0001264
MGI:104565	Cdkn1b	"Cdk2<tm1Kald>/Cdk2<tm1Kald>,Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>"	involves: 129S1/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0004765	decreased brainstem auditory evoked potential	CCO:MP0004765
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0006325	impaired hearing	CCO:MP0006325
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<+>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<+>,Crebbp<tm1Jvd>/Crebbp<tm1Jvd>,Tg(MMTV-cre)4Mam/0"	involves: 129 * C57BL/6 * CBA	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0002038	carcinoma	CCO:MP0002038
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0000042	abnormal organ of Corti	CCO:MP0000042
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6NHsd	MP:0004401	increased cochlear outer hair cell number	CCO:MP0004401
MGI:104565	Cdkn1b	Cdkn1b<tm2.1Mlf>/Cdkn1b<tm2.1Mlf>	involves: 129S4/SvJaeSor	MP:0002083	premature death	CCO:MP0002083
MGI:104565	Cdkn1b	Cdkn1b<tm3Mlf>/Cdkn1b<tm3Mlf>	involves: 129S4/SvJaeSor	MP:0002083	premature death	CCO:MP0002083
MGI:104565	Cdkn1b	Cdkn1b<tm3Mlf>/Cdkn1b<tm3Mlf>	involves: 129S4/SvJaeSor	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104565	Cdkn1b	"Cdkn1b<tm3Mlf>/Cdkn1b<tm3Mlf>,Tg(Pomc1-cre)1Mlf/0"	involves: 129S4/SvJaeSor	MP:0002083	premature death	CCO:MP0002083
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0008371	pituitary intermediate lobe hyperplasia	CCO:MP0008371
MGI:104565	Cdkn1b	"Cdkn1b<tm3Mlf>/Cdkn1b<tm3Mlf>,Tg(Pomc1-cre)1Mlf/0"	involves: 129S4/SvJaeSor	MP:0005514	increased resistance to tumor development	CCO:MP0005514
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0001263	weight loss	CCO:MP0001263
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Tg(KRT5-CDK4)2303Mlrp/0"	involves: 129S4/SvJae * C57BL/6 * FVB * SENCAR * SSIN	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0001148	enlarged testes	CCO:MP0001148
MGI:104565	Cdkn1b	Cdkn1b<tm3Mlf>/Cdkn1b<tm3Mlf>	involves: 129S4/SvJaeSor	MP:0001264	increased body size	CCO:MP0001264
MGI:104565	Cdkn1b	"Cdkn1b<tm2Mlf>/Cdkn1b<tm2Mlf>,Tg(Pomc1-cre)1Mlf/0"	involves: 129S4/SvJaeSor	MP:0002083	premature death	CCO:MP0002083
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL	MP:0000274	enlarged heart	CCO:MP0000274
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL	MP:0000275	heart hyperplasia	CCO:MP0000275
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL	MP:0002833	increased heart weight	CCO:MP0002833
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL	MP:0003567	abnormal fetal cardiomyocyte proliferation	CCO:MP0003567
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Tg(KRT5-CDK4)2303Mlrp/0"	involves: 129S4/SvJae * C57BL/6 * FVB * SENCAR * SSIN	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL	MP:0004565	small myocardial fiber	CCO:MP0004565
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL	MP:0006321	increased myocardial fiber number	CCO:MP0006321
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0001393	ataxia	CCO:MP0001393
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000274	enlarged heart	CCO:MP0000274
MGI:104565	Cdkn1b	"Cdkn1b<tm2Mlf>/Cdkn1b<tm2Mlf>,Tg(Pomc1-cre)1Mlf/0"	involves: 129S4/SvJaeSor	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<+>,Myc<tm1Atp>/Myc<+>"	involves: 129P2/OlaHsd * 129S4/SvJaeSor * FVB/N	MP:0001265	decreased body size	CCO:MP0001265
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Myc<tm1Atp>/Myc<tm1Atp>"	involves: 129P2/OlaHsd * 129S4/SvJaeSor * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Myc<tm1Atp>/Myc<+>"	involves: 129P2/OlaHsd * 129S4/SvJaeSor * FVB/N	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Myc<tm1Atp>/Myc<+>"	involves: 129P2/OlaHsd * 129S4/SvJaeSor * FVB/N	MP:0001265	decreased body size	CCO:MP0001265
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0006262	testis tumor	CCO:MP0006262
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Rbx1<Gt(XB674)Byg>/Rbx1<Gt(XB674)Byg>"	involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:104565	Cdkn1b	Cdkn1b<tm1Jro>/Cdkn1b<tm1Jro>	involves: 129S4/SvJaeSor * C57BL/6	MP:0009584	decreased keratinocyte proliferation	CCO:MP0009584
MGI:104565	Cdkn1b	Cdkn1b<tm1Jro>/Cdkn1b<tm1Jro>	involves: 129S4/SvJaeSor * C57BL/6	MP:0002908	delayed wound healing	CCO:MP0002908
MGI:104565	Cdkn1b	Cdkn1b<tm1Jro>/Cdkn1b<tm1Jro>	involves: 129S4/SvJaeSor * C57BL/6	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:104565	Cdkn1b	Cdkn1b<tm1Jro>/Cdkn1b<tm1Jro>	involves: 129S4/SvJaeSor * C57BL/6	MP:0001260	increased body weight	CCO:MP0001260
MGI:104565	Cdkn1b	Cdkn1b<tm1Jro>/Cdkn1b<tm1Jro>	involves: 129S4/SvJaeSor * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<tm1.1Ctre>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<tm1.1Ctre>"	involves: 129/Sv * 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:104565	Cdkn1b	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0001260	increased body weight	CCO:MP0001260
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0009363	abnormal secondary ovarian follicle morphology	CCO:MP0009363
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0008130	abnormal pituitary intermediate lobe	CCO:MP0008130
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0009092	endometrium hyperplasia	CCO:MP0009092
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0008939	increased pituitary gland weight	CCO:MP0008939
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0008868	abnormal granulosa cell morphology	CCO:MP0008868
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000635	pituitary gland hyperplasia	CCO:MP0000635
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0008301	adrenal medulla hyperplasia	CCO:MP0008301
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0008105	increased amacrine cell number	CCO:MP0008105
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0004958	enlarged prostate	CCO:MP0004958
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0008371	pituitary intermediate lobe hyperplasia	CCO:MP0008371
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0000642	enlarged adrenal glands	CCO:MP0000642
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0004832	enlarged ovary	CCO:MP0004832
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0006069	abnormal retinal neuronal layer morphology	CCO:MP0006069
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000636	enlarged pituitary gland	CCO:MP0000636
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000840	abnormal epithalamus morphology	CCO:MP0000840
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0001328	disorganized retinal layers	CCO:MP0001328
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0001926	female infertility	CCO:MP0001926
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000703	abnormal thymus morphology	CCO:MP0000703
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor * C57BL/6J	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0004952	increased spleen weight	CCO:MP0004952
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001264	increased body size	CCO:MP0001264
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0009017	prolonged estrus	CCO:MP0009017
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0009006	prolonged estrous cycle	CCO:MP0009006
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0008371	pituitary intermediate lobe hyperplasia	CCO:MP0008371
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0004955	increased thymus weight	CCO:MP0004955
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0002679	abnormal corpus luteum	CCO:MP0002679
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0000714	increased thymocyte number	CCO:MP0000714
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0001260	increased body weight	CCO:MP0001260
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Tg(MMTV-vHaras)SH1Led/0"	involves: 129S4/SvJaeSor * C57BL/6J * CD-1	MP:0003721	increased tumor growth/size	CCO:MP0003721
MGI:104565	Cdkn1b	Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>	involves: 129S1/Sv * C57BL/6	MP:0008130	abnormal pituitary intermediate lobe	CCO:MP0008130
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0005551	abnormal eye electrophysiology	CCO:MP0005551
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0005201	abnormal retinal pigment epithelium morphology	CCO:MP0005201
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0005015	increased T cell number	CCO:MP0005015
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001328	disorganized retinal layers	CCO:MP0001328
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001260	increased body weight	CCO:MP0001260
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0002064	seizures	CCO:MP0002064
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001120	abnormal uterus morphology	CCO:MP0001120
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001149	testicular hyperplasia	CCO:MP0001149
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001148	enlarged testes	CCO:MP0001148
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0005547	abnormal Muller cell morphology	CCO:MP0005547
MGI:104565	Cdkn1b	Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001004	abnormal retinal photoreceptor morphology	CCO:MP0001004
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0004143	hypertonia	CCO:MP0004143
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001429	dehydration	CCO:MP0001429
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0005150	cachexia	CCO:MP0005150
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0004760	increased mitotic index	CCO:MP0004760
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0000754	paresis	CCO:MP0000754
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0004924	abnormal behavior	CCO:MP0004924
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001999	photosensitivity	CCO:MP0001999
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0008569	lethality at weaning	CCO:MP0008569
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0000745	tremors	CCO:MP0000745
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001263	weight loss	CCO:MP0001263
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0002882	abnormal neuron morphology	CCO:MP0002882
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001513	limb grasping	CCO:MP0001513
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0005156	bradykinesia	CCO:MP0005156
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001523	impaired righting response	CCO:MP0001523
MGI:104565	Cdkn1b	Cdkn1b<tm3Jro>/Cdkn1b<tm3Jro>	involves: 129S4/SvJaeSor	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104565	Cdkn1b	Cdkn1b<tm3Jro>/Cdkn1b<tm3Jro>	involves: 129S4/SvJaeSor	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:104565	Cdkn1b	Cdkn1b<tm3Jro>/Cdkn1b<+>	involves: 129S4/SvJaeSor	MP:0001264	increased body size	CCO:MP0001264
MGI:104565	Cdkn1b	Cdkn1b<tm2Jro>/Cdkn1b<tm2Jro>	involves: 129S4/SvJaeSor * C57BL/6	MP:0004502	decreased incidence of chemically-induced tumors	CCO:MP0004502
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129/Sv * C57BL/6J	MP:0009171	enlarged pancreatic islets	CCO:MP0009171
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J * C3H * NIH	MP:0002083	premature death	CCO:MP0002083
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0001261	obese	CCO:MP0001261
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0001433	polyphagia	CCO:MP0001433
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<+>	involves: 129S4/SvJaeSor	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:104565	Cdkn1b	Cdkn1b<tm3Jro>/Cdkn1b<tm3Jro>	involves: 129S4/SvJaeSor	MP:0001264	increased body size	CCO:MP0001264
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001260	increased body weight	CCO:MP0001260
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001961	abnormal reflex	CCO:MP0001961
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001148	enlarged testes	CCO:MP0001148
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor	MP:0002225	abnormal spleen cellularity	CCO:MP0002225
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0001328	disorganized retinal layers	CCO:MP0001328
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:104565	Cdkn1b	Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>	involves: 129S4/SvJaeSor	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:104565	Cdkn1b	Cdkn1b<tm3Jro>/Cdkn1b<tm3Jro>	involves: 129S4/SvJaeSor	MP:0001260	increased body weight	CCO:MP0001260
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J * C3H * NIH	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0001548	hyperlipidemia	CCO:MP0001548
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0005534	decreased body temperature	CCO:MP0005534
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0001559	hyperglycemia	CCO:MP0001559
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0001261	obese	CCO:MP0001261
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129/Sv * C57BL/6J	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:104565	Cdkn1b	"Ccnd1<tm1Dsn>/Ccnd1<tm1Dsn>,Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>"	involves: 129/Sv * C57BL/6	MP:0002679	abnormal corpus luteum	CCO:MP0002679
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0001433	polyphagia	CCO:MP0001433
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0003645	increased pancreatic beta cell number	CCO:MP0003645
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129/Sv * C57BL/6J	MP:0005559	increased circulating glucose level	CCO:MP0005559
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J * C3H * NIH	MP:0002032	sarcoma	CCO:MP0002032
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0003645	increased pancreatic beta cell number	CCO:MP0003645
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129/Sv * C57BL/6J	MP:0009171	enlarged pancreatic islets	CCO:MP0009171
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Nkx3-1<tm1.1Saa>/Nkx3-1<tm1.1Saa>"	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	MP:0009219	prostate intraepithelial neoplasia	CCO:MP0009219
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Nkx3-1<tm1.1Saa>/Nkx3-1<tm1.1Saa>"	involves: 129S4/SvJaeSor * C57BL/6 * FVB/N	MP:0002009	preneoplasia	CCO:MP0002009
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129/Sv * C57BL/6J	MP:0005559	increased circulating glucose level	CCO:MP0005559
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J * C3H * NIH	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0005534	decreased body temperature	CCO:MP0005534
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129/Sv * C57BL/6J	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:104565	Cdkn1b	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0001548	hyperlipidemia	CCO:MP0001548
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Lepr<db>/Lepr<db>"	involves: C57BL/6J * C57BLKS/J	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129/Sv * C57BL/6J	MP:0003645	increased pancreatic beta cell number	CCO:MP0003645
MGI:104565	Cdkn1b	"Cdkn1b<tm1Kin>/Cdkn1b<tm1Kin>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129/Sv * C57BL/6J	MP:0003645	increased pancreatic beta cell number	CCO:MP0003645
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004819	decreased skeletal muscle mass	CCO:MP0004819
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002581	abnormal ileum morphology	CCO:MP0002581
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0003052	omphalocele	CCO:MP0003052
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0003237	abnormal lens epithelium morphology	CCO:MP0003237
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0003613	abnormal kidney medulla development	CCO:MP0003613
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004002	abnormal jejunum morphology	CCO:MP0004002
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004174	abnormal spine curvature	CCO:MP0004174
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004320	split sternum	CCO:MP0004320
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0008148	abnormal rib-sternum attachment	CCO:MP0008148
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0009399	increased skeletal muscle fiber size	CCO:MP0009399
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000761	thin diaphragm muscle	CCO:MP0000761
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0009546	absent gastric milk in neonates	CCO:MP0009546
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0005160	proteinuria	CCO:MP0005160
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002294	short gestation period	CCO:MP0002294
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0001575	cyanosis	CCO:MP0001575
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0003123	paternal imprinting	CCO:MP0003123
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0003158	dysphagia	CCO:MP0003158
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003123	paternal imprinting	CCO:MP0003123
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001436	abnormal suckling behavior	CCO:MP0001436
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004321	short sternum	CCO:MP0004321
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000526	small inner medullary pyramid	CCO:MP0000526
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000153	rib bifurcation	CCO:MP0000153
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002264	abnormal bronchus morphology	CCO:MP0002264
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002270	abnormal respiratory alveoli morphology	CCO:MP0002270
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000131	abnormal long bone epiphysis morphology	CCO:MP0000131
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000157	abnormal sternum morphology	CCO:MP0000157
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000757	herniated abdominal wall	CCO:MP0000757
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002842	increased blood pressure	CCO:MP0002842
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	either: (involves: 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * ICR)	MP:0003237	abnormal lens epithelium morphology	CCO:MP0003237
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002267	abnormal bronchiole morphology	CCO:MP0002267
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	either: (involves: 129S7/SvEvBrd * C57BL/6) or (involves: 129S7/SvEvBrd * ICR)	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003123	paternal imprinting	CCO:MP0003123
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000642	enlarged adrenal glands	CCO:MP0000642
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:104564	Cdkn1c	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Cdkn1c<tm1Sje>/Cdkn1c<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:104564	Cdkn1c	"Cdkn1c<tm1Sje>/Cdkn1c<+>,Kcnq1ot1<tm1Tilg>/Kcnq1ot1<+>"	involves: 129 * C57BL/6	MP:0003787	abnormal imprinting	CCO:MP0003787
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0006144	increased systolic blood pressure	CCO:MP0006144
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<+>	involves: 129 * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0005160	proteinuria	CCO:MP0005160
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0000523	cortical renal glomerulopathies	CCO:MP0000523
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0004920	increased placenta weight	CCO:MP0004920
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0002703	abnormal renal tubule morphology	CCO:MP0002703
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0006144	increased systolic blood pressure	CCO:MP0006144
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0000523	cortical renal glomerulopathies	CCO:MP0000523
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0002703	abnormal renal tubule morphology	CCO:MP0002703
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0005160	proteinuria	CCO:MP0005160
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd	MP:0004920	increased placenta weight	CCO:MP0004920
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003257	abnormal abdominal wall	CCO:MP0003257
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003055	abnormal long bone epiphyseal plate morphology	CCO:MP0003055
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003052	omphalocele	CCO:MP0003052
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003123	paternal imprinting	CCO:MP0003123
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000642	enlarged adrenal glands	CCO:MP0000642
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000111	cleft palate	CCO:MP0000111
MGI:104564	Cdkn1c	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129/Sv * C57BL/6J	MP:0004894	uterus atrophy	CCO:MP0004894
MGI:104564	Cdkn1c	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129/Sv * C57BL/6J	MP:0004193	abnormal kidney papilla morphology	CCO:MP0004193
MGI:104564	Cdkn1c	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129/Sv * C57BL/6J	MP:0003568	uterus atresia	CCO:MP0003568
MGI:104564	Cdkn1c	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129/Sv * C57BL/6J	MP:0003257	abnormal abdominal wall	CCO:MP0003257
MGI:104564	Cdkn1c	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129/Sv * C57BL/6J	MP:0003123	paternal imprinting	CCO:MP0003123
MGI:104564	Cdkn1c	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129/Sv * C57BL/6J	MP:0003052	omphalocele	CCO:MP0003052
MGI:104564	Cdkn1c	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129/Sv * C57BL/6J	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:104564	Cdkn1c	Cdkn1c<tm1.1(Cdkn1b*)Kei>/Cdkn1c<+>	involves: 129/Sv * C57BL/6J	MP:0000642	enlarged adrenal glands	CCO:MP0000642
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001304	cataracts	CCO:MP0001304
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003568	uterus atresia	CCO:MP0003568
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004894	uterus atrophy	CCO:MP0004894
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004686	decreased length of long bones	CCO:MP0004686
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004193	abnormal kidney papilla morphology	CCO:MP0004193
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003052	omphalocele	CCO:MP0003052
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001575	cyanosis	CCO:MP0001575
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0002357	abnormal spleen white pulp morphology	CCO:MP0002357
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001938	delayed sexual maturation	CCO:MP0001938
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0000057	abnormal osteogenesis	CCO:MP0000057
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0003158	dysphagia	CCO:MP0003158
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001139	abnormal vagina morphology	CCO:MP0001139
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0002163	abnormal gland morphology	CCO:MP0002163
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0004258	abnormal placenta size	CCO:MP0004258
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0004920	increased placenta weight	CCO:MP0004920
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002163	abnormal gland morphology	CCO:MP0002163
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0004255	abnormal spongiotrophoblast layer morphology	CCO:MP0004255
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0005296	abnormal humerus morphology	CCO:MP0005296
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0003572	abnormal uterus development	CCO:MP0003572
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002581	abnormal ileum morphology	CCO:MP0002581
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000757	herniated abdominal wall	CCO:MP0000757
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000131	abnormal long bone epiphysis morphology	CCO:MP0000131
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000759	abnormal skeletal muscle morphology	CCO:MP0000759
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000526	small inner medullary pyramid	CCO:MP0000526
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000897	abnormal midbrain morphology	CCO:MP0000897
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000057	abnormal osteogenesis	CCO:MP0000057
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000131	abnormal long bone epiphysis morphology	CCO:MP0000131
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003613	abnormal kidney medulla development	CCO:MP0003613
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0002059	abnormal seminal gland morphology	CCO:MP0002059
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004002	abnormal jejunum morphology	CCO:MP0004002
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002581	abnormal ileum morphology	CCO:MP0002581
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004320	split sternum	CCO:MP0004320
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004686	decreased length of long bones	CCO:MP0004686
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008151	increased diameter of long bones	CCO:MP0008151
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008794	increased lens epithelium apoptosis	CCO:MP0008794
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001436	abnormal suckling behavior	CCO:MP0001436
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:104564	Cdkn1c	Cdkn1c<tm1Sje>/Cdkn1c<tm1Sje>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003723	abnormal long bone morphology	CCO:MP0003723
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0000462	abnormal digestive system morphology	CCO:MP0000462
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001158	abnormal prostate morphology	CCO:MP0001158
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:104564	Cdkn1c	Cdkn1c<tm1Kat>/Cdkn1c<tm1Kat>	involves: 129P2/OlaHsd * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002113	abnormal skeleton development	CCO:MP0002113
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000498	absent jejunum	CCO:MP0000498
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003119	abnormal digestive system development	CCO:MP0003119
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0009546	absent gastric milk in neonates	CCO:MP0009546
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003756	abnormal hard palate	CCO:MP0003756
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003419	delayed endochondral bone ossification	CCO:MP0003419
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003271	abnormal duodenum morphology	CCO:MP0003271
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003154	abnormal soft palate	CCO:MP0003154
MGI:104564	Cdkn1c	Cdkn1c<tm1Bbd>/Cdkn1c<tm1Bbd>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002116	abnormal craniofacial bone morphology	CCO:MP0002116
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<+>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129 * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0000160	kyphosis	CCO:MP0000160
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0003155	abnormal telomere length	CCO:MP0003155
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0003786	premature aging	CCO:MP0003786
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0001262	decreased body weight	CCO:MP0001262
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<+>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129 * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)89.1Dam/0"	involves: C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	FVB.Cg-Cdkn2a<tm1Rdp>	MP:0001304	cataracts	CCO:MP0001304
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	FVB.Cg-Cdkn2a<tm1Rdp>	MP:0001297	microphthalmia	CCO:MP0001297
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	FVB.Cg-Cdkn2a<tm1Rdp>	MP:0001004	abnormal retinal photoreceptor morphology	CCO:MP0001004
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	FVB.Cg-Cdkn2a<tm1Rdp>	MP:0002699	abnormal vitreous body	CCO:MP0002699
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	FVB.Cg-Cdkn2a<tm1Rdp>	MP:0005195	abnormal posterior eye segment morphology	CCO:MP0005195
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	FVB.Cg-Cdkn2a<tm1Rdp>	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	FVB.Cg-Cdkn2a<tm1Rdp>	MP:0006069	abnormal retinal neuronal layer morphology	CCO:MP0006069
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S/SvEv * C57BL/6 * CBA * FVB/N	MP:0006079	stomach tumor	CCO:MP0006079
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Pdgfrb<tm1Sor>/Pdgfrb<tm1Sor>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	MP:0002699	abnormal vitreous body	CCO:MP0002699
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0003236	abnormal lens capsule morphology	CCO:MP0003236
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0001289	persistence of hyaloid capillary system	CCO:MP0001289
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S/SvEv * C57BL/6 * CBA * FVB/N	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S/SvEv * C57BL/6 * CBA * FVB/N	MP:0006079	stomach tumor	CCO:MP0006079
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S/SvEv * C57BL/6 * CBA * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S/SvEv * C57BL/6 * CBA * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>"	involves: 129 * FVB/N	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S/SvEv * C57BL/6 * CBA * FVB/N	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S/SvEv * C57BL/6 * CBA * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S/SvEv * C57BL/6 * CBA * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>"	involves: 129 * FVB/N	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>"	involves: 129 * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>"	involves: 129 * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Braf<tm1Mmcm>/Braf<+>,Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>"	Not Specified	MP:0008014	lung tumor	CCO:MP0008014
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0001265	decreased body size	CCO:MP0001265
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>,Smad4<tm1Rdp>/Smad4<tm1Rdp>"	involves: 129 * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Terc<tm1Rdp>/Terc<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)89.1Dam/0"	involves: C57BL/6 * CBA	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>"	involves: 129S1/Sv * 129X1/SvJ	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>"	involves: 129S1/Sv * 129X1/SvJ	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>"	involves: 129S1/Sv * 129X1/SvJ	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<+>,Kras<tm4Tyj>/Kras<+>,Ptf1a<tm1.1(cre)Cvw>/Ptf1a<+>"	involves: 129S1/Sv * 129X1/SvJ	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0002014	papilloma	CCO:MP0002014
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0003721	increased tumor growth/size	CCO:MP0003721
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(tetO-BRAF*V600E)29Lc/0,Tg(Tyr-rtTA)37Lc/0"	involves: 129/Sv * C57BL/6J * SJL	MP:0009220	prostate adenocarcinoma	CCO:MP0009220
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(tetO-BRAF*V600E)29Lc/0,Tg(Tyr-rtTA)37Lc/0"	involves: 129/Sv * C57BL/6J * SJL	MP:0001158	abnormal prostate morphology	CCO:MP0001158
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(tetO-BRAF*V600E)29Lc/0,Tg(Tyr-rtTA)37Lc/0"	involves: 129/Sv * C57BL/6J * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0002038	carcinoma	CCO:MP0002038
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(GFAP-TVA)10Ech/0"	involves: 129 * BALB/c * C57BL/6 * FVB/N * SJL	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0003721	increased tumor growth/size	CCO:MP0003721
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<+>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0002014	papilloma	CCO:MP0002014
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Brn>/Cdkn2a<tm2.1Brn>	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<+>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0002038	carcinoma	CCO:MP0002038
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2a/Cdkn2b<tm2Brn>	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0002038	carcinoma	CCO:MP0002038
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0000599	enlarged liver	CCO:MP0000599
MGI:104738	Cdkn2a	Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>	involves: 129P2/OlaHsd * FVB/N	MP:0004502	decreased incidence of chemically-induced tumors	CCO:MP0004502
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Dicer1<tm1Snjo>/Dicer1<tm1Snjo>"	involves: 129/Sv * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,X/Tg(Tyr-HRAS)60Lc"	involves: 129/Sv * C57BL/6J * CBA/J * FVB/N * SJL	MP:0001304	cataracts	CCO:MP0001304
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Gt(ROSA)26Sor<tm1.1(MYC/ESR1)Gev>/Gt(ROSA)26Sor<tm1.1(MYC/ESR1)Gev>"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(S100b-v-erbB)4496Waw/0"	involves: 129/Sv * C57BL/6J * DBA/2J * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(S100b-v-erbB)4496Waw/0"	involves: 129/Sv * C57BL/6J * DBA/2J * FVB/N * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Tg(S100b-v-erbB)4496Waw/0"	involves: 129/Sv * C57BL/6J * DBA/2J * FVB/N * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,X/Tg(Tyr-HRAS)60Lc"	involves: 129/Sv * C57BL/6J * CBA/J * FVB/N * SJL	MP:0006246	tumor of uvea	CCO:MP0006246
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,X/Tg(Tyr-HRAS)60Lc"	involves: 129/Sv * C57BL/6J * CBA/J * FVB/N * SJL	MP:0004501	increased incidence of UV-induced tumors	CCO:MP0004501
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Cdkn2b<tm2Brn>/Cdkn2b<tm2Brn>"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<+>,Pdgfra<tm12Sor>/Pdgfra<+>"	involves: 129 * 129/Sv * C57BL/6J * SJL	MP:0003045	fibrosis	CCO:MP0003045
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd	MP:0005276	skin tumor	CCO:MP0005276
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Col1a1<tm1(CAG-EGFR)Char>/Col1a1<tm1(CAG-EGFR)Char>,Pten<tm1Hwu>/Pten<tm1Hwu>"	involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd	MP:0002026	leukemia	CCO:MP0002026
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<+>	involves: 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2a/Cdkn2b<tm1Brn>	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Col1a1<tm1(CAG-EGFR)Char>/Col1a1<tm2(CAG-EGFR*)Char>,Pten<tm1Hwu>/Pten<tm1Hwu>"	involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Col1a1<tm1(CAG-EGFR)Char>/Col1a1<tm2(CAG-EGFR*)Char>,Pten<tm1Hwu>/Pten<tm1Hwu>"	involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Col1a1<tm2(CAG-EGFR*)Char>/Col1a1<tm2(CAG-EGFR*)Char>,Pten<tm1Hwu>/Pten<tm1Hwu>"	involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Col1a1<tm2(CAG-EGFR*)Char>/Col1a1<tm2(CAG-EGFR*)Char>,Pten<tm1Hwu>/Pten<tm1Hwu>"	involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Col1a1<tm1(CAG-EGFR)Char>/Col1a1<tm1(CAG-EGFR)Char>,Pten<tm1Hwu>/Pten<tm1Hwu>"	involves: 129/Sv * 129S4/SvJae * C57BL/6 * SJL	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Brn>/Cdkn2a<tm2.1Brn>	involves: 129P2/OlaHsd * FVB/N	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(GFAP-TVA)5Hev/0"	involves: 129/Sv * C57BL/6 * SJL	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(Tyr-NRAS*Q61K)1Bee/?"	involves: 129/Sv * C57BL/6 * CBA * SJL	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(Tyr-NRAS*Q61K)1Bee/?"	involves: 129/Sv * C57BL/6 * CBA * SJL	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(Tyr-NRAS*Q61K)1Bee/?"	involves: 129/Sv * C57BL/6 * CBA * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0009336	increased splenocyte proliferation	CCO:MP0009336
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0008078	increased CD8-positive T cell number	CCO:MP0008078
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0008074	increased CD4-positive T cell number	CCO:MP0008074
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0004955	increased thymus weight	CCO:MP0004955
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0005091	increased double-positive T cell number	CCO:MP0005091
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:104738	Cdkn2a	"Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>,Nf1<tm1Tyj>/Nf1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(Tyr-NRAS*Q61K)1Bee/?"	involves: 129/Sv * C57BL/6 * CBA * SJL	MP:0008014	lung tumor	CCO:MP0008014
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(GFAP-TVA)5Hev/0"	involves: 129/Sv * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<+>,Pdgfra<tm12Sor>/Pdgfra<+>"	involves: 129 * 129/Sv * C57BL/6J * SJL	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<+>,Pdgfra<tm12Sor>/Pdgfra<+>"	involves: 129 * 129/Sv * C57BL/6J * SJL	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(NES-TVA)12Hev/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(NES-TVA)12Hev/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(NES-TVA)12Hev/0"	involves: 129/Sv * C57BL/6 * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(NES-TVA)12Hev/0"	involves: 129/Sv * C57BL/6 * FVB/N * SJL	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>,Tg(NES-TVA)12Hev/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>,Tg(NES-TVA)12Hev/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002026	leukemia	CCO:MP0002026
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Cdkn2b<tm2Brn>/Cdkn2b<tm2Brn>"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2a<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(GFAP-TVA)5Hev/0"	involves: 129X1/SvJ * C57BL/6	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Tg(NES-TVA)12Hev/0"	involves: 129 * C57BL/6 * FVB/N * SJL	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>,Tg(GFAP-TVA)5Hev/0"	involves: 129S6/SvEvTac * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>,Tg(GFAP-TVA)5Hev/0"	involves: 129S6/SvEvTac * C57BL/6	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(GFAP-TVA)5Hev/0"	involves: 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	Cdkn2a<tm2.1Rdp>/Cdkn2a<+>	involves: 129S6/SvEvTac * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Nf1<tm1Tyj>/Nf1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<+>,Pdgfra<tm12Sor>/Pdgfra<+>"	involves: 129 * 129/Sv * C57BL/6J * SJL	MP:0003851	skeletal muscle interstitial fibrosis	CCO:MP0003851
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(GFAP-TVA)10Ech/0"	involves: 129 * BALB/c * C57BL/6 * FVB/N * SJL	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Nf1<tm1Tyj>/Nf1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(NES-TVA)12Hev/0"	involves: 129 * C57BL/6 * FVB/N * SJL	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Nf1<tm1Tyj>/Nf1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(Tyr-NRAS*Q61K)1Bee/?"	involves: 129/Sv * C57BL/6 * CBA * SJL	MP:0008019	liver tumor	CCO:MP0008019
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Nf1<tm1Tyj>/Nf1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0002026	leukemia	CCO:MP0002026
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(NES-TVA)12Hev/0"	involves: 129 * C57BL/6 * FVB/N * SJL	MP:0009277	brain tumor	CCO:MP0009277
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Tg(Tyr-NRAS*Q61K)1Bee/?"	involves: 129/Sv * C57BL/6 * CBA * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Nf1<tm1Tyj>/Nf1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<+>,Kat5<tm1Jwl>/Kat5<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<+>"	involves: 129P2/OlaHsd	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	Cdkn2a<tm3(cre)Cjs>/Cdkn2a<tm4Cjs>	involves: 129S1/Sv * C57BL/6	MP:0002001	blindness	CCO:MP0002001
MGI:104738	Cdkn2a	Cdkn2a<tm3(cre)Cjs>/Cdkn2a<tm4Cjs>	involves: 129S1/Sv * C57BL/6	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0003570	uterus leiomyoma	CCO:MP0003570
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<+>"	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a<tm3(cre)Cjs>/Cdkn2a<tm4Cjs>	involves: 129S1/Sv * C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0002026	leukemia	CCO:MP0002026
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd * FVB/N	MP:0008019	liver tumor	CCO:MP0008019
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Myf6<tm1(cre)Mrc>/Myf6<+>,Pax3<tm1Mrc>/Pax3<tm1Mrc>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd * FVB/N	MP:0005623	abnormal meninges morphology	CCO:MP0005623
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd * FVB/N	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a<tm3(cre)Cjs>/Cdkn2a<tm4Cjs>	involves: 129S1/Sv * C57BL/6	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:104738	Cdkn2a	Cdkn2a<tm3(cre)Cjs>/Cdkn2a<+>	involves: 129S1/Sv * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:104738	Cdkn2a	"Cdkn2a<tm1Sxs>/Cdkn2a<+>,Tgfb2<tm1Doe>/Tgfb2<tm1Doe>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Braf<tm1Cpri>/Braf<tm1Cpri>,Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(Tyr-cre/ERT2)1Laru/0"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2 * SJL	MP:0005276	skin tumor	CCO:MP0005276
MGI:104738	Cdkn2a	"Braf<tm1Cpri>/Braf<tm1Cpri>,Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(Tyr-cre/ERT2)1Laru/0"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2 * SJL	MP:0002018	malignant tumors	CCO:MP0002018
MGI:104738	Cdkn2a	"Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>,Tgfb2<tm1Doe>/Tgfb2<+>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0000599	enlarged liver	CCO:MP0000599
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<+>"	involves: 129P2/OlaHsd	MP:0002026	leukemia	CCO:MP0002026
MGI:104738	Cdkn2a	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a<tm1Sxs>/Cdkn2a<tm1Sxs>	involves: 129/Sv * C57BL/6	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:104738	Cdkn2a	Cdkn2a<tm1Sxs>/Cdkn2a<tm1Sxs>	involves: 129/Sv * C57BL/6	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:104738	Cdkn2a	"Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>,Tgfb2<tm1Doe>/Tgfb2<tm1Doe>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:104738	Cdkn2a	Cdkn2a<tm1Sxs>/Cdkn2a<tm1Sxs>	involves: 129/Sv * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<+>,Tgfb2<tm1Doe>/Tgfb2<tm1Doe>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0000599	enlarged liver	CCO:MP0000599
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<tm2Brn>,Nf2<tm2Gth>/Nf2<+>"	involves: 129P2/OlaHsd	MP:0003570	uterus leiomyoma	CCO:MP0003570
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0002026	leukemia	CCO:MP0002026
MGI:104738	Cdkn2a	"Cdkn2a<tm2Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>"	involves: 129P2/OlaHsd	MP:0003570	uterus leiomyoma	CCO:MP0003570
MGI:104738	Cdkn2a	Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>	involves: 129S1/Sv * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Tg(MT-HGFSF)18Lmb/0"	involves: 129/Sv * C57BL/6J * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:104738	Cdkn2a	Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>	involves: 129S1/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>	involves: 129S1/Sv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0003099	retinal detachment	CCO:MP0003099
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0003733	abnormal retinal inner nuclear layer morphology	CCO:MP0003733
MGI:104738	Cdkn2a	Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>	involves: 129S1/Sv * C57BL/6	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ	MP:0002001	blindness	CCO:MP0002001
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ	MP:0002673	abnormal sperm number	CCO:MP0002673
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0004500	increased incidence of ionizing radiation-induced tumors	CCO:MP0004500
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0005241	abnormal retinal ganglion layer morphology	CCO:MP0005241
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0001004	abnormal retinal photoreceptor morphology	CCO:MP0001004
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0002037	fibrohistocytoma	CCO:MP0002037
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0001289	persistence of hyaloid capillary system	CCO:MP0001289
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:104738	Cdkn2a	Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>	involves: 129S1/Sv * C57BL/6	MP:0004500	increased incidence of ionizing radiation-induced tumors	CCO:MP0004500
MGI:104738	Cdkn2a	Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>	involves: 129S1/Sv * C57BL/6	MP:0009321	histiocytic sarcoma	CCO:MP0009321
MGI:104738	Cdkn2a	Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>	involves: 129S1/Sv * C57BL/6	MP:0009515	gastrointestinal stromal tumor	CCO:MP0009515
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: FVB/N	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:104738	Cdkn2a	Cdkn2a<tm1Nesh>/Cdkn2a<tm1Nesh>	involves: 129S6/SvEvTac * FVB/N	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:104738	Cdkn2a	"Cdkn2a<tm2.1Rdp>/Cdkn2a<tm2.1Rdp>,Tg(Tyr-HRAS)60Lc/?"	involves: 129S6/SvEvTac * C57BL/6J * CBA/J * FVB	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Nesh>/Cdkn2a<tm1Nesh>,X/Tg(Tyr-HRAS)60Lc"	involves: 129S6/SvEvTac * C57BL/6J * CBA/J * FVB	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)89.1Dam/0"	involves: C57BL/6 * CBA	MP:0009152	pancreatic intraepithelial neoplasia	CCO:MP0009152
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)89.1Dam/0"	involves: C57BL/6 * CBA	MP:0009151	pancreatic ductal adenocarcinoma	CCO:MP0009151
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)89.1Dam/0"	involves: C57BL/6 * CBA	MP:0002018	malignant tumors	CCO:MP0002018
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0008478	increased spleen white pulp amount	CCO:MP0008478
MGI:104738	Cdkn2a	Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>	involves: 129X1/SvJ * C57BL/6	MP:0003236	abnormal lens capsule morphology	CCO:MP0003236
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0002356	abnormal spleen red pulp morphology	CCO:MP0002356
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104738	Cdkn2a	Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>	involves: 129/Sv * C57BL/6 * SJL	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:104738	Cdkn2a	"Cdkn2a<tm4Rdp>/Cdkn2a<tm4Rdp>,Kras<tm4Tyj>/Kras<+>,Tg(Pdx1-cre)89.1Dam/0"	involves: C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)76Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)76Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)76Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)76Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002026	leukemia	CCO:MP0002026
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)76Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)76Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)76Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002026	leukemia	CCO:MP0002026
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002022	lymphoma	CCO:MP0002022
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002032	sarcoma	CCO:MP0002032
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:104738	Cdkn2a	Cdkn2a<Pctr1-DBA/2N>/?	involves: BALB/cAnPt * DBA/2N	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:104738	Cdkn2a	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Mxi1<tm1Rdp>/Mxi1<tm1Rdp>"	involves: 129/Sv * C57BL/6J * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104738	Cdkn2a	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Tg(CAG-sb10)1Dla/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129X1/SvJ * FVB/N	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd	MP:0002026	leukemia	CCO:MP0002026
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2a/Cdkn2b<tm1Brn>	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002032	sarcoma	CCO:MP0002032
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002026	leukemia	CCO:MP0002026
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd	MP:0002022	lymphoma	CCO:MP0002022
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002022	lymphoma	CCO:MP0002022
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104737	Cdkn2b	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Cdkn2b<tm2Brn>/Cdkn2b<tm2Brn>"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2a/Cdkn2b<tm2Brn>	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104737	Cdkn2b	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Cdkn2b<tm2Brn>/Cdkn2b<tm2Brn>"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm2Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd	MP:0005276	skin tumor	CCO:MP0005276
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:104737	Cdkn2b	Cdkn2a/Cdkn2b<tm1Brn>/Cdkn2b<+>	involves: 129P2/OlaHsd	MP:0002032	sarcoma	CCO:MP0002032
MGI:104737	Cdkn2b	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0000688	lymphoid hyperplasia	CCO:MP0000688
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0000688	lymphoid hyperplasia	CCO:MP0000688
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0001148	enlarged testes	CCO:MP0001148
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:104737	Cdkn2b	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0001264	increased body size	CCO:MP0001264
MGI:104737	Cdkn2b	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104737	Cdkn2b	Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0001429	dehydration	CCO:MP0001429
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000636	enlarged pituitary gland	CCO:MP0000636
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000642	enlarged adrenal glands	CCO:MP0000642
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000274	enlarged heart	CCO:MP0000274
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0002083	premature death	CCO:MP0002083
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Ptch1<tm1Mps>/Ptch1<+>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Ptch1<tm1Mps>/Ptch1<+>"	involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0001148	enlarged testes	CCO:MP0001148
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0001263	weight loss	CCO:MP0001263
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0008371	pituitary intermediate lobe hyperplasia	CCO:MP0008371
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0002038	carcinoma	CCO:MP0002038
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0001393	ataxia	CCO:MP0001393
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>"	involves: 129/Sv * 129S1/Sv * C57BL/6 * DBA/2	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:105388	Cdkn2c	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:105388	Cdkn2c	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0008014	lung tumor	CCO:MP0008014
MGI:105388	Cdkn2c	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	B6.129-Cdkn2c<tm1Yxi>	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	B6.129-Cdkn2c<tm1Yxi>	MP:0002048	lung adenoma	CCO:MP0002048
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	B6.129-Cdkn2c<tm1Yxi>	MP:0008014	lung tumor	CCO:MP0008014
MGI:105388	Cdkn2c	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:105388	Cdkn2c	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<tm1.1Ctre>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:105388	Cdkn2c	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0006262	testis tumor	CCO:MP0006262
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	B6.129-Cdkn2c<tm1Yxi>	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:105388	Cdkn2c	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<tm1.1Ctre>"	involves: 129/Sv * 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:105388	Cdkn2c	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0009308	adenocarcinoma	CCO:MP0009308
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001750	increased circulating follicle stimulating hormone level	CCO:MP0001750
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0000630	mammary gland hyperplasia	CCO:MP0000630
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002780	decreased circulating testosterone level	CCO:MP0002780
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0001264	increased body size	CCO:MP0001264
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0000889	abnormal cerebellar molecular layer	CCO:MP0000889
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0001152	Leydig cell hyperplasia	CCO:MP0001152
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0001148	enlarged testes	CCO:MP0001148
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0001429	dehydration	CCO:MP0001429
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002786	abnormal Leydig cell morphology	CCO:MP0002786
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0000635	pituitary gland hyperplasia	CCO:MP0000635
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0002780	decreased circulating testosterone level	CCO:MP0002780
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0002786	abnormal Leydig cell morphology	CCO:MP0002786
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0001264	increased body size	CCO:MP0001264
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0000523	cortical renal glomerulopathies	CCO:MP0000523
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0001148	enlarged testes	CCO:MP0001148
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001260	increased body weight	CCO:MP0001260
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0001147	small testis	CCO:MP0001147
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0002444	abnormal T cell physiology	CCO:MP0002444
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0001393	ataxia	CCO:MP0001393
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0002364	abnormal thymus size	CCO:MP0002364
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0005014	increased B cell number	CCO:MP0005014
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0005015	increased T cell number	CCO:MP0005015
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0008130	abnormal pituitary intermediate lobe	CCO:MP0008130
MGI:105388	Cdkn2c	Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>	involves: 129S1/Sv * C57BL/6	MP:0001264	increased body size	CCO:MP0001264
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000636	enlarged pituitary gland	CCO:MP0000636
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001152	Leydig cell hyperplasia	CCO:MP0001152
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000635	pituitary gland hyperplasia	CCO:MP0000635
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002209	decreased germ cell number	CCO:MP0002209
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002208	abnormal germ cell morphology	CCO:MP0002208
MGI:105388	Cdkn2c	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000642	enlarged adrenal glands	CCO:MP0000642
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0001260	increased body weight	CCO:MP0001260
MGI:105388	Cdkn2c	Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>	involves: 129/Sv * C57BL/6 * DBA/2	MP:0001263	weight loss	CCO:MP0001263
MGI:105388	Cdkn2c	"Cdkn2b<tm1Bbd>/Cdkn2b<tm1Bbd>,Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>"	involves: 129S1/Sv * C57BL/6	MP:0000688	lymphoid hyperplasia	CCO:MP0000688
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6 * CD-1	MP:0004749	nonsyndromic hearing loss	CCO:MP0004749
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6 * CD-1	MP:0004740	sensorineural hearing loss	CCO:MP0004740
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6 * CD-1	MP:0004362	cochlear hair cell degeneration	CCO:MP0004362
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6 * CD-1	MP:0004398	cochlear inner hair cell degeneration	CCO:MP0004398
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6 * CD-1	MP:0004404	cochlear outer hair cell degeneration	CCO:MP0004404
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6 * CD-1	MP:0004432	abnormal cochlear hair cell physiology	CCO:MP0004432
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6 * CD-1	MP:0004737	absent distortion product otoacoustic emissions	CCO:MP0004737
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6 * CD-1	MP:0004765	decreased brainstem auditory evoked potential	CCO:MP0004765
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6	MP:0001750	increased circulating follicle stimulating hormone level	CCO:MP0001750
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129P2/OlaHsd * C57BL/6	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:105387	Cdkn2d	Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>	involves: 129X1/SvJ * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001999	photosensitivity	CCO:MP0001999
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001429	dehydration	CCO:MP0001429
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002208	abnormal germ cell morphology	CCO:MP0002208
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002786	abnormal Leydig cell morphology	CCO:MP0002786
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001263	weight loss	CCO:MP0001263
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001260	increased body weight	CCO:MP0001260
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0000745	tremors	CCO:MP0000745
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0008569	lethality at weaning	CCO:MP0008569
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0004924	abnormal behavior	CCO:MP0004924
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001513	limb grasping	CCO:MP0001513
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0004760	increased mitotic index	CCO:MP0004760
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0000754	paresis	CCO:MP0000754
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0004143	hypertonia	CCO:MP0004143
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0005150	cachexia	CCO:MP0005150
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0005156	bradykinesia	CCO:MP0005156
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001523	impaired righting response	CCO:MP0001523
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002780	decreased circulating testosterone level	CCO:MP0002780
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0002882	abnormal neuron morphology	CCO:MP0002882
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:105387	Cdkn2d	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129X1/SvJ * C57BL/6	MP:0002064	seizures	CCO:MP0002064
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001152	Leydig cell hyperplasia	CCO:MP0001152
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002209	decreased germ cell number	CCO:MP0002209
MGI:105387	Cdkn2d	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Cdkn2d<tm1Maro>/Cdkn2d<tm1Maro>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0001750	increased circulating follicle stimulating hormone level	CCO:MP0001750
MGI:1098230	Cenpe	Cenpe<tm1Dwc>/Cenpe<tm2Dwc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1098230	Cenpe	Cenpe<tm1Dwc>/Cenpe<tm1Dwc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1098230	Cenpe	Cenpe<tm2Dwc>/Cenpe<tm2Dwc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002658	abnormal liver regeneration	CCO:MP0002658
MGI:1098230	Cenpe	Cenpe<tm2Dwc>/Cenpe<tm2Dwc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1098230	Cenpe	Cenpe<tm1Dwc>/Cenpe<tm1Dwc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1098230	Cenpe	Cenpe<tm2Dwc>/Cenpe<tm2Dwc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:1098230	Cenpe	Cenpe<tm1Dwc>/Cenpe<tm1Dwc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:1351331	Chaf1a	Chaf1a<tm1Ger>/Chaf1a<tm1Ger>	involves: 129S2/SvPasCrl	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1351331	Chaf1a	Chaf1a<tm1Ger>/Chaf1a<tm1Ger>	involves: 129S2/SvPasCrl	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1351331	Chaf1a	Chaf1a<tm1Ger>/Chaf1a<tm1Ger>	involves: 129S2/SvPasCrl	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1202065	Chek1	Chek1<tm1Sje>/Chek1<tm1Sje>	Not Specified	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:1202065	Chek1	Chek1<tm1Mkt>/Chek1<tm1Mkt>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1202065	Chek1	Chek1<tm1Mkt>/Chek1<tm1Mkt>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1202065	Chek1	Chek1<tm1Mkt>/Chek1<tm1Mkt>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1202065	Chek1	Chek1<tm1Mkt>/Chek1<tm1Mkt>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1202065	Chek1	Chek1<tm1Mkt>/Chek1<tm1Mkt>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1202065	Chek1	Chek1<tm1Mkt>/Chek1<tm1Mkt>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:1202065	Chek1	Chek1<tm1Sje>/Chek1<tm1Sje>	Not Specified	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1202065	Chek1	Chek1<tm1Sje>/Chek1<tm1Sje>	Not Specified	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1202065	Chek1	Chek1<tm1Sje>/Chek1<tm1Sje>	Not Specified	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1202065	Chek1	Chek1<tm1Sje>/Chek1<tm1Sje>	Not Specified	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1202065	Chek1	"Chek1<tm1Sje>/Chek1<tm1Sje>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1202065	Chek1	"Chek1<tm1Sje>/Chek1<+>,Tg(Wnt1)1Hev/0"	Not Specified	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:1202065	Chek1	"Chek1<tm1Sje>/Chek1<tm1Sje>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1202065	Chek1	"Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Wap-cre)11738Mam/0"	involves: C57BL/6	MP:0001882	abnormal lactation	CCO:MP0001882
MGI:1202065	Chek1	"Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Wap-cre)11738Mam/0"	involves: C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1202065	Chek1	"Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Wap-cre)11738Mam/0"	involves: C57BL/6	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:1202065	Chek1	"Chek1<tm1Jmr>/Chek1<tm1Jmr>,Tg(Wap-cre)11738Mam/0"	involves: C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:1202065	Chek1	"Chek1<tm1Jmr>/Chek1<+>,Tg(Wap-cre)11738Mam/0"	involves: C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1355321	Chek2	Chek2<tm1Pjs>/Chek2<tm1Pjs>	involves: 129/Sv * Black Swiss * FVB/N	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1355321	Chek2	"Brca1<tm2Mak>/Brca1<tm2Mak>,Chek2<tm1Mak>/Chek2<tm1Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1355321	Chek2	Chek2<tm1Pjs>/Chek2<tm1Pjs>	involves: 129/Sv * Black Swiss * FVB/N	MP:0004025	polyploidy	CCO:MP0004025
MGI:1355321	Chek2	Chek2<tm1Pjs>/Chek2<tm1Pjs>	involves: 129/Sv * Black Swiss * FVB/N	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1355321	Chek2	Chek2<tm1Mak>/Chek2<tm1Mak>	involves: 129P2/OlaHsd	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:1355321	Chek2	"Brca1<tm2Mak>/Brca1<tm2Mak>,Chek2<tm1Mak>/Chek2<tm1Mak>,Tg(Lck-cre)548Jxm/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:1355321	Chek2	"Brca1<tm2Mak>/Brca1<tm2Mak>,Chek2<tm1Mak>/Chek2<tm1Mak>,Tg(Wap-cre)11738Mam/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:1355321	Chek2	Chek2<tm1Mak>/Chek2<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:1355321	Chek2	Chek2<tm1Mak>/Chek2<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1355321	Chek2	Chek2<tm1Mak>/Chek2<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:1355321	Chek2	"Chek2<tm1Mak>/Chek2<tm1Mak>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:1355321	Chek2	"Chek2<tm1Mak>/Chek2<tm1Mak>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1355321	Chek2	Chek2<tm1Nmt>/Chek2<tm1Nmt>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003010	decreased mortality induced by ionizing radiation	CCO:MP0003010
MGI:1355321	Chek2	Chek2<tm1Nmt>/Chek2<tm1Nmt>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1355321	Chek2	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:1355321	Chek2	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0005432	abnormal pro-B cell morphology	CCO:MP0005432
MGI:1355321	Chek2	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:1355321	Chek2	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1355321	Chek2	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<tm1Jc>	involves: 129S/SvEv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<tm1Jc>	involves: 129S/SvEv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<tm1Jc>	involves: 129S/SvEv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<tm1Jc>	involves: 129S/SvEv * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<tm1Jc>	involves: 129S/SvEv * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<tm1Jc>	involves: 129S/SvEv * C57BL/6	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<+>	involves: 129S/SvEv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<+>	involves: 129S/SvEv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<+>	involves: 129S/SvEv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:2444898	Chfr	Chfr<tm1Jc>/Chfr<+>	involves: 129S/SvEv * C57BL/6	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001393	ataxia	CCO:MP0001393
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000745	tremors	CCO:MP0000745
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001406	abnormal gait	CCO:MP0001406
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000897	abnormal midbrain morphology	CCO:MP0000897
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000830	abnormal diencephalon morphology	CCO:MP0000830
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000849	abnormal cerebellum morphology	CCO:MP0000849
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002741	small olfactory bulb	CCO:MP0002741
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002685	abnormal spermatogonia proliferation	CCO:MP0002685
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000852	small cerebellum	CCO:MP0000852
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002906	increased susceptibility to pharmacologically induced seizures	CCO:MP0002906
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000875	abnormal cerebellar Purkinje cell layer	CCO:MP0000875
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000812	abnormal dentate gyrus morphology	CCO:MP0000812
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000819	abnormal olfactory bulb morphology	CCO:MP0000819
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000243	myoclonus	CCO:MP0000243
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:105313	Cit	Cit<tm1Fdc>/Cit<tm1Fdc>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0008540	abnormal cerebrum morphology	CCO:MP0008540
MGI:1306784	Cited2	Cited2<tm1.2Dunw>/Cited2<tm1.2Dunw>	involves: 129S1/Sv * C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1306784	Cited2	Cited2<tm1.2Dunw>/Cited2<tm1.2Dunw>	involves: 129S1/Sv * C57BL/6J	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:1306784	Cited2	Cited2<tm1.2Dunw>/Cited2<tm1.2Dunw>	involves: 129S1/Sv * C57BL/6J	MP:0000914	exencephaly	CCO:MP0000914
MGI:1306784	Cited2	"Cited1<tm1Fmar>/Cited1<tm1Fmar>,Cited2<tm1Bha>/Cited2<tm1Bha>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1306784	Cited2	Cited2<tm1Dunw>/Cited2<tm1Dunw>	involves: 129S1/Sv * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd	MP:0000527	abnormal kidney development	CCO:MP0000527
MGI:1306784	Cited2	Cited2<tm1.2Dunw>/Cited2<tm1.2Dunw>	involves: 129S1/Sv * C57BL/6J	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:1306784	Cited2	Cited2<tm1.1Dunw>/Cited2<tm1.1Dunw>	involves: 129S1/Sv * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Wnt1-cre)11Rth/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0001093	small trigeminal ganglion	CCO:MP0001093
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(T-cre)1Lwd/0"	involves: 129 * C3H * C57BL/6 * SJL	MP:0000531	right pulmonary isomerism	CCO:MP0000531
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Wnt1-cre)11Rth/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0003987	small vestibular ganglion	CCO:MP0003987
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Wnt1-cre)11Rth/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0000914	exencephaly	CCO:MP0000914
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Wnt1-cre)11Rth/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0001096	abnormal glossopharyngeal ganglion morphology	CCO:MP0001096
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(T-cre)1Lwd/0"	involves: 129 * C3H * C57BL/6 * SJL	MP:0003921	abnormal heart left ventricle morphology	CCO:MP0003921
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(T-cre)1Lwd/0"	involves: 129 * C3H * C57BL/6 * SJL	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<+>	involves: 129P2/OlaHsd	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(T-cre)1Lwd/0"	involves: 129 * C3H * C57BL/6 * SJL	MP:0005313	absent adrenal gland	CCO:MP0005313
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(T-cre)1Lwd/0"	involves: 129 * C3H * C57BL/6 * SJL	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<+>	involves: 129P2/OlaHsd	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<+>	involves: 129P2/OlaHsd	MP:0000486	abnormal pulmonary trunk morphology	CCO:MP0000486
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<+>	involves: 129P2/OlaHsd	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: 129 * C57BL/6 * CBA * SJL	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd	MP:0005313	absent adrenal gland	CCO:MP0005313
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Wnt1-cre)11Rth/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0000914	exencephaly	CCO:MP0000914
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(T-cre)1Lwd/0"	involves: 129 * C3H * C57BL/6 * SJL	MP:0000644	dextrocardia	CCO:MP0000644
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(T-cre)1Lwd/0"	involves: 129 * C3H * C57BL/6 * SJL	MP:0006061	right atrial isomerism	CCO:MP0006061
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Wnt1-cre)11Rth/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0004158	right aortic arch	CCO:MP0004158
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0004110	transposition of great arteries	CCO:MP0004110
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0003921	abnormal heart left ventricle morphology	CCO:MP0003921
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Wnt1-cre)11Rth/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0001100	abnormal vagus ganglion morphology	CCO:MP0001100
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Wnt1-cre)11Rth/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0001083	small geniculate ganglion	CCO:MP0001083
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd	MP:0004158	right aortic arch	CCO:MP0004158
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0002745	abnormal atrioventricular valve morphology	CCO:MP0002745
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0006063	abnormal inferior vena cava morphology	CCO:MP0006063
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0006061	right atrial isomerism	CCO:MP0006061
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<+>	involves: 129P2/OlaHsd	MP:0001785	edema	CCO:MP0001785
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0000644	dextrocardia	CCO:MP0000644
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0000531	right pulmonary isomerism	CCO:MP0000531
MGI:1306784	Cited2	"Cited2<tm1Bha>/Cited2<tm2Bha>,Tg(Sox2-cre)1Amc/0"	involves: 129 * C57BL/6 * CBA * SJL	MP:0005313	absent adrenal gland	CCO:MP0005313
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000531	right pulmonary isomerism	CCO:MP0000531
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003105	abnormal heart atrium morphology	CCO:MP0003105
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006065	abnormal heart position	CCO:MP0006065
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005313	absent adrenal gland	CCO:MP0005313
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006061	right atrial isomerism	CCO:MP0006061
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005294	abnormal heart ventricle morphology	CCO:MP0005294
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0006135	arterial stenosis	CCO:MP0006135
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002745	abnormal atrioventricular valve morphology	CCO:MP0002745
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002949	abnormal neural crest cells	CCO:MP0002949
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0000914	exencephaly	CCO:MP0000914
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0001322	abnormal iris morphology	CCO:MP0001322
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000914	exencephaly	CCO:MP0000914
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001700	abnormal embryo turning	CCO:MP0001700
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002111	abnormal tail morphology	CCO:MP0002111
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0005262	coloboma	CCO:MP0005262
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000964	small dorsal root ganglion	CCO:MP0000964
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0002745	abnormal atrioventricular valve morphology	CCO:MP0002745
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0004837	abnormal neural fold formation	CCO:MP0004837
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0000914	exencephaly	CCO:MP0000914
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0000438	abnormal skull morphology	CCO:MP0000438
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000527	abnormal kidney development	CCO:MP0000527
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0000929	open neural tube	CCO:MP0000929
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0001081	abnormal cranial ganglia morphology	CCO:MP0001081
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004157	interrupted aortic arch	CCO:MP0004157
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004158	right aortic arch	CCO:MP0004158
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004252	abnormal direction of looping morphogenesis	CCO:MP0004252
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000692	small spleen	CCO:MP0000692
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001081	abnormal cranial ganglia morphology	CCO:MP0001081
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006063	abnormal inferior vena cava morphology	CCO:MP0006063
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000963	fused dorsal root ganglion	CCO:MP0000963
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<+>	involves: C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<+>	involves: C57BL/6J	MP:0000914	exencephaly	CCO:MP0000914
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<+>	involves: C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0000233	abnormal blood flow velocity	CCO:MP0000233
MGI:1306784	Cited2	Cited2<tm1Ycy>/Cited2<tm1Ycy>	involves: C57BL/6J	MP:0009688	abnormal spinal cord central canal morphology	CCO:MP0009688
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:1306784	Cited2	Cited2<tm1Jpmb>/Cited2<tm1Jpmb>	involves: 129P2/OlaHsd * C57BL/6	MP:0000963	fused dorsal root ganglion	CCO:MP0000963
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0002111	abnormal tail morphology	CCO:MP0002111
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0001700	abnormal embryo turning	CCO:MP0001700
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0000692	small spleen	CCO:MP0000692
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0002745	abnormal atrioventricular valve morphology	CCO:MP0002745
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0002766	situs inversus	CCO:MP0002766
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0006061	right atrial isomerism	CCO:MP0006061
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0006065	abnormal heart position	CCO:MP0006065
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0004157	interrupted aortic arch	CCO:MP0004157
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0004158	right aortic arch	CCO:MP0004158
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0004252	abnormal direction of looping morphogenesis	CCO:MP0004252
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129/Sv * C57BL/6J	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	involves: 129/Sv * C57BL/6J	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0000531	right pulmonary isomerism	CCO:MP0000531
MGI:1306784	Cited2	Cited2<tm1Bha>/Cited2<tm1Bha>	B6.129P2-Cited2<tm1Bha>	MP:0006063	abnormal inferior vena cava morphology	CCO:MP0006063
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<tm1Sir>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0001273	decreased metastatic potential	CCO:MP0001273
MGI:1889208	Cks1b	Cks1b<tm1Sir>/Cks1b<tm1Sir>	Not Specified	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:1889208	Cks1b	Cks1b<tm1Sir>/Cks1b<+>	Not Specified	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<tm1Sir>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<tm1Sir>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<tm1Sir>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<tm1Sir>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0005093	decreased B cell proliferation	CCO:MP0005093
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<tm1Sir>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0004953	decreased spleen weight	CCO:MP0004953
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<+>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<+>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:1889208	Cks1b	Cks1b<tm1Sir>/Cks1b<tm1Sir>	Not Specified	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1889208	Cks1b	"Cks1b<tm1Sir>/Cks1b<tm1Sir>,Tg(IghMyc)22Bri/?"	involves: C57BL * C57BL/6 * SJL	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:1913447	Cks2	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1913447	Cks2	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1913447	Cks2	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:1913447	Cks2	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1913447	Cks2	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	MP:0005159	azoospermia	CCO:MP0005159
MGI:1913447	Cks2	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	MP:0001925	male infertility	CCO:MP0001925
MGI:1913447	Cks2	Cks2<tm1Sir>/Cks2<tm1Sir>	Not Specified	MP:0001926	female infertility	CCO:MP0001926
MGI:1923749	Clasp2	Clasp2<tm1Gal>/Clasp2<tm1Gal>	Not Specified	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1923749	Clasp2	Clasp2<tm1Gal>/Clasp2<tm1Gal>	Not Specified	MP:0003091	abnormal cell migration	CCO:MP0003091
MGI:107472	Clgn	Clgn<tm1Osb>/Clgn<tm1Osb>	either: 129 or (involves: 129P2/OlaHsd * C57BL/6J)	MP:0000242	impaired fertilization	CCO:MP0000242
MGI:107472	Clgn	Clgn<tm1Osb>/Clgn<tm1Osb>	either: 129 or (involves: 129P2/OlaHsd * C57BL/6J)	MP:0001925	male infertility	CCO:MP0001925
MGI:1349415	Cops5	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1349415	Cops5	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:1349415	Cops5	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0,Tg(TcraTcrb)425Cbn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1349415	Cops5	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0006413	increased T cell apoptosis	CCO:MP0006413
MGI:1349415	Cops5	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1349415	Cops5	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1349415	Cops5	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0002375	abnormal thymus medulla morphology	CCO:MP0002375
MGI:1349415	Cops5	Cops5<tm1Rpar>/Cops5<tm1Rpar>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1349415	Cops5	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0008083	decreased single-positive T cell number	CCO:MP0008083
MGI:1349415	Cops5	Cops5<tm1Jka>/Cops5<+>	involves: 129S4/SvJae * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1349415	Cops5	Cops5<tm1Jka>/Cops5<+>	involves: 129S4/SvJae * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:1349415	Cops5	Cops5<tm1Jka>/Cops5<tm1Jka>	involves: 129S4/SvJae * C57BL/6	MP:0001696	failure to gastrulate	CCO:MP0001696
MGI:1349415	Cops5	Cops5<tm1Jka>/Cops5<tm1Jka>	involves: 129S4/SvJae * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1349415	Cops5	Cops5<tm1Jka>/Cops5<tm1Jka>	involves: 129S4/SvJae * C57BL/6	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:1349415	Cops5	Cops5<tm1Jka>/Cops5<tm1Jka>	involves: 129S4/SvJae * C57BL/6	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1349415	Cops5	Cops5<tm1Jka>/Cops5<tm1Jka>	involves: 129S4/SvJae * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1349415	Cops5	Cops5<tm1Jka>/Cops5<tm1Jka>	involves: 129S4/SvJae * C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003578	absent ovary	CCO:MP0003578
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003582	abnormal ovary development	CCO:MP0003582
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002207	abnormal long term potentiation	CCO:MP0002207
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:108442	Cpeb1	Cpeb1<tm1Rcht>/Cpeb1<tm1Rcht>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:3529431	Crocc	Crocc<tm1Tili>/Crocc<tm1Tili>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001861	lung inflammation	CCO:MP0001861
MGI:3529431	Crocc	Crocc<tm1Tili>/Crocc<tm1Tili>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008450	retinal photoreceptor degeneration	CCO:MP0008450
MGI:88515	Cryaa	"Cryaa<L1N>/Cryaa<L1N>,Tg(CAG-EGFP)1Osb/0"	involves: C3H * C57BL/6	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:88515	Cryaa	Cryaa<L1N>/Cryaa<+>	involves: C3H/HeN * C57BL/6J	MP:0001306	small lens	CCO:MP0001306
MGI:88515	Cryaa	Cryaa<L1N>/Cryaa<+>	involves: C3H/HeN * C57BL/6J	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<L1N>/Cryaa<L1N>	involves: C3H/HeN * C57BL/6J	MP:0001306	small lens	CCO:MP0001306
MGI:88515	Cryaa	Cryaa<2J>/Cryaa<2J>	involves: BALB/c * FVB/N	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<2J>/Cryaa<2J>	involves: BALB/c * FVB/N	MP:0001306	small lens	CCO:MP0001306
MGI:88515	Cryaa	Cryaa<L1N>/Cryaa<L1N>	involves: C3H/HeN * C57BL/6J	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<2J>/Cryaa<2J>	involves: BALB/c * FVB/N	MP:0001297	microphthalmia	CCO:MP0001297
MGI:88515	Cryaa	"Cryaa<2J>/Cryaa<2J>,Tg(CAG-EGFP)1Osb/0"	involves: BALB/c * C3H * C57BL/6 * FVB/N	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:88515	Cryaa	"Cryaa<2J>/Cryaa<2J>,Tg(CAG-EGFP)1Osb/0"	involves: BALB/c * C3H * C57BL/6 * FVB/N	MP:0003237	abnormal lens epithelium morphology	CCO:MP0003237
MGI:88515	Cryaa	"Cryaa<2J>/Cryaa<2J>,Tg(CAG-EGFP)1Osb/0"	involves: BALB/c * C3H * C57BL/6 * FVB/N	MP:0003236	abnormal lens capsule morphology	CCO:MP0003236
MGI:88515	Cryaa	Cryaa<tm1.1Ady>/Cryaa<+>	involves: 129 * C57BL/6	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:88515	Cryaa	Cryaa<tm1.1Ady>/Cryaa<tm1.1Ady>	involves: 129 * C57BL/6	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:88515	Cryaa	Cryaa<tm1.1Ady>/Cryaa<tm1.1Ady>	involves: 129 * C57BL/6	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<tm1.1Ady>/Cryaa<tm1.1Ady>	involves: 129 * C57BL/6	MP:0001306	small lens	CCO:MP0001306
MGI:88515	Cryaa	Cryaa<tm1.1Ady>/Cryaa<tm1.1Ady>	involves: 129 * C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:88515	Cryaa	Cryaa<tm1.1Ady>/Cryaa<tm1.1Ady>	involves: 129 * C57BL/6	MP:0008796	increased lens fiber apoptosis	CCO:MP0008796
MGI:88515	Cryaa	Cryaa<tm1.1Ady>/Cryaa<tm1.1Ady>	involves: 129 * C57BL/6	MP:0008794	increased lens epithelium apoptosis	CCO:MP0008794
MGI:88515	Cryaa	Cryaa<tm1.1Ady>/Cryaa<+>	involves: 129 * C57BL/6	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<Aey7>/Cryaa<+>	C3HeB/FeJ	MP:0001297	microphthalmia	CCO:MP0001297
MGI:88515	Cryaa	Cryaa<Aey7>/Cryaa<Aey7>	C3HeB/FeJ	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<+>	involves: 129/Sv * 129S4/SvJae	MP:0001306	small lens	CCO:MP0001306
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<+>	involves: 129S4/SvJae * C57BL/6 * DBA/2	MP:0001306	small lens	CCO:MP0001306
MGI:88515	Cryaa	Cryaa<lop18>/Cryaa<lop18>	CBA/CaGnLeJ	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:88515	Cryaa	Cryaa<lop18>/Cryaa<lop18>	CBA/CaGnLeJ	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<lop18>/Cryaa<lop18>	CBA/CaGnLeJ	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<tm1Wawr>	involves: 129/Sv * 129S4/SvJae	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<Aey7>/Cryaa<+>	C3HeB/FeJ	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:88515	Cryaa	Cryaa<Aey7>/Cryaa<Aey7>	C3HeB/FeJ	MP:0001297	microphthalmia	CCO:MP0001297
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<tm1Wawr>	involves: 129/Sv * 129S4/SvJae	MP:0001306	small lens	CCO:MP0001306
MGI:88515	Cryaa	Cryaa<Aey7>/Cryaa<Aey7>	C3HeB/FeJ	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<tm1Wawr>	involves: 129S4/SvJae * C57BL/6 * DBA/2	MP:0008794	increased lens epithelium apoptosis	CCO:MP0008794
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<tm1Wawr>	involves: 129S4/SvJae * C57BL/6 * DBA/2	MP:0001297	microphthalmia	CCO:MP0001297
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<tm1Wawr>	involves: 129S4/SvJae * C57BL/6 * DBA/2	MP:0001306	small lens	CCO:MP0001306
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<tm1Wawr>	involves: 129S4/SvJae * C57BL/6 * DBA/2	MP:0001304	cataracts	CCO:MP0001304
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<tm1Wawr>	involves: 129/Sv * 129S4/SvJae	MP:0008794	increased lens epithelium apoptosis	CCO:MP0008794
MGI:88515	Cryaa	Cryaa<tm1Wawr>/Cryaa<tm1Wawr>	involves: 129/Sv * 129S4/SvJae	MP:0001297	microphthalmia	CCO:MP0001297
MGI:88515	Cryaa	Cryaa<Aey7>/Cryaa<+>	C3HeB/FeJ	MP:0001304	cataracts	CCO:MP0001304
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0009237	kinked sperm flagellum	CCO:MP0009237
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0002674	abnormal sperm motility	CCO:MP0002674
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0002686	globozoospermia	CCO:MP0002686
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0009230	abnormal sperm head morphology	CCO:MP0009230
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0009231	detached acrosome	CCO:MP0009231
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0009232	abnormal sperm nucleus morphology	CCO:MP0009232
MGI:88547	Csnk2a2	Csnk2a2<tm1Dcs>/Csnk2a2<tm1Dcs>	involves: 129S6/SvEvTac * C57BL/6	MP:0005578	teratozoospermia	CCO:MP0005578
MGI:1917264	Csrp2bp	Csrp2bp<Gt(OST388291)Lex>/Csrp2bp<Gt(OST388291)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0004261	abnormal embryonic neuroepithelium morphology	CCO:MP0004261
MGI:1917264	Csrp2bp	Csrp2bp<Gt(OST388291)Lex>/Csrp2bp<Gt(OST388291)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1917264	Csrp2bp	Csrp2bp<Gt(OST388291)Lex>/Csrp2bp<Gt(OST388291)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1917264	Csrp2bp	Csrp2bp<Gt(OST388291)Lex>/Csrp2bp<Gt(OST388291)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1917264	Csrp2bp	Csrp2bp<Gt(OST388291)Lex>/Csrp2bp<Gt(OST388291)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1913765	Cul7	Cul7<tm1Zqp>/Cul7<tm1Zqp>	involves: 129S/SvEv * C57BL/6J	MP:0004201	fetal growth retardation	CCO:MP0004201
MGI:1913765	Cul7	Cul7<tm1Zqp>/Cul7<tm1Zqp>	involves: 129S/SvEv * C57BL/6J	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:1913765	Cul7	Cul7<tm1Zqp>/Cul7<tm1Zqp>	involves: 129S/SvEv * C57BL/6J	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1913765	Cul7	Cul7<tm1Jdec>/Cul7<tm1Jdec>	involves: C57BL/6 * CD-1	MP:0001712	abnormal placenta development	CCO:MP0001712
MGI:1913765	Cul7	Cul7<tm1Jdec>/Cul7<tm1Jdec>	involves: C57BL/6 * CD-1	MP:0001954	respiratory distress	CCO:MP0001954
MGI:1913765	Cul7	Cul7<tm1Jdec>/Cul7<tm1Jdec>	involves: C57BL/6 * CD-1	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1913765	Cul7	Cul7<tm1Jdec>/Cul7<tm1Jdec>	involves: C57BL/6 * CD-1	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1913765	Cul7	Cul7<tm1Jdec>/Cul7<tm1Jdec>	involves: C57BL/6 * CD-1	MP:0001713	decreased trophoblast giant cell number	CCO:MP0001713
MGI:1913765	Cul7	Cul7<tm1Jdec>/Cul7<tm1Jdec>	involves: C57BL/6 * CD-1	MP:0000259	abnormal vascular development	CCO:MP0000259
MGI:1913765	Cul7	Cul7<tm1Jdec>/Cul7<tm1Jdec>	involves: C57BL/6 * CD-1	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1925559	Cul9	Cul9<tm1Jdec>/Cul9<tm1Jdec>	involves: C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1202881	Cuzd1	Cuzd1<tm1Ljm>/Cuzd1<tm1Ljm>	involves: 129S6/SvEvTac * Black Swiss	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:1202881	Cuzd1	Cuzd1<tm1Ljm>/Cuzd1<tm1Ljm>	involves: 129S6/SvEvTac * Black Swiss	MP:0004761	increased susceptibility to induced pancreatitis	CCO:MP0004761
MGI:2176159	Cyp26b1	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	MP:0001954	respiratory distress	CCO:MP0001954
MGI:2176159	Cyp26b1	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:2176159	Cyp26b1	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:2176159	Cyp26b1	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:2176159	Cyp26b1	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	MP:0001147	small testis	CCO:MP0001147
MGI:2176159	Cyp26b1	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:2176159	Cyp26b1	Cyp26b1<tm1.1Ptk>/Cyp26b1<tm1.1Ptk>	involves: 129S2/SvPas	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002639	micrognathia	CCO:MP0002639
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000556	abnormal hindlimb morphology	CCO:MP0000556
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001705	abnormal proximal-distal axis patterning	CCO:MP0001705
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000547	short limbs	CCO:MP0000547
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000565	oligodactyly	CCO:MP0000565
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:2176159	Cyp26b1	Cyp26b1<tm1Hh>/Cyp26b1<tm1Hh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:1197015	Daxx	Daxx<tm2Led>/Daxx<tm2Led>	involves: 129S1/SvImJ * 129S6/SvEvTac	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0004261	abnormal embryonic neuroepithelium morphology	CCO:MP0004261
MGI:1197015	Daxx	Daxx<tm1Maul>/Daxx<tm1Maul>	involves: 129/Sv	MP:0003708	binucleate	CCO:MP0003708
MGI:1197015	Daxx	Daxx<tm1Maul>/Daxx<tm1Maul>	involves: 129/Sv	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1197015	Daxx	Daxx<tm1Maul>/Daxx<tm1Maul>	involves: 129/Sv	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0002582	disorganized extraembryonic tissue	CCO:MP0002582
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	129S6/SvEvTac	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001675	abnormal ectoderm development	CCO:MP0001675
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0003891	increased allantois apoptosis	CCO:MP0003891
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0006386	absent somites	CCO:MP0006386
MGI:1197015	Daxx	Daxx<tm1Led>/Daxx<tm1Led>	involves: 129S6/SvEvTac * Black Swiss	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1342328	Dazl	"Dazl<tm1Hjc>/Dazl<+>,Pum2<Gt(XE772)Byg>/Pum2<Gt(XE772)Byg>"	involves: 129P2/OlaHsd * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<+>	involves: 129P2/OlaHsd * MF1	MP:0006362	abnormal male germ cell morphology	CCO:MP0006362
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<+>	involves: 129P2/OlaHsd * MF1	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	MP:0001925	male infertility	CCO:MP0001925
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	MP:0001926	female infertility	CCO:MP0001926
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	MP:0001147	small testis	CCO:MP0001147
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	MP:0001127	small ovary	CCO:MP0001127
MGI:1342328	Dazl	Dazl<tm1Hjc>/Dazl<tm1Hjc>	involves: 129P2/OlaHsd * MF1	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1930042	Dclre1a	Dclre1a<tm1Remo>/Dclre1a<tm1Remo>	involves: 129X1/SvJ	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:1930042	Dclre1a	"Dclre1a<tm1Remo>/Dclre1a<tm1Remo>,Fancd2<tm1Hou>/Fancd2<tm1Hou>"	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1930042	Dclre1a	Dclre1a<tm1Roka>/Dclre1a<tm1Roka>	Not Specified	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1930042	Dclre1a	Dclre1a<tm1Roka>/Dclre1a<tm1Roka>	Not Specified	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:109247	Ddit3	Ddit3<tm1Mori>/Ddit3<tm1Mori>	involves: 129P2/OlaHsd	MP:0002176	increased brain weight	CCO:MP0002176
MGI:109247	Ddit3	Ddit3<tm1Dron>/Ddit3<tm1Dron>	involves: 129S1/Sv * 129X1/SvJ * FVB/N	MP:0002410	decreased susceptibility to viral infection	CCO:MP0002410
MGI:109247	Ddit3	Ddit3<tm1Mori>/Ddit3<tm1Mori>	involves: 129P2/OlaHsd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:109247	Ddit3	Ddit3<tm1Dron>/Ddit3<tm1Dron>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0005164	abnormal response to injury	CCO:MP0005164
MGI:109247	Ddit3	Ddit3<tm1Dron>/Ddit3<tm1Dron>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:109247	Ddit3	Ddit3<tm1Mori>/Ddit3<tm1Mori>	involves: 129P2/OlaHsd * C57BL/6	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0001152	Leydig cell hyperplasia	CCO:MP0001152
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0002286	cryptorchism	CCO:MP0002286
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129/Sv	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	MP:0008279	arrest of spermiogenesis	CCO:MP0008279
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0001147	small testis	CCO:MP0001147
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	MP:0001147	small testis	CCO:MP0001147
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	MP:0005159	azoospermia	CCO:MP0005159
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	MP:0005159	azoospermia	CCO:MP0005159
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	MP:0002784	abnormal Sertoli cell morphology	CCO:MP0002784
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	MP:0001925	male infertility	CCO:MP0001925
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	MP:0001147	small testis	CCO:MP0001147
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	MP:0002784	abnormal Sertoli cell morphology	CCO:MP0002784
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0006420	abnormal peritubular myoid cell morphology	CCO:MP0006420
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0006421	decreased number of peritubular myoid cells	CCO:MP0006421
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0001925	male infertility	CCO:MP0001925
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0006418	abnormal testis cord formation	CCO:MP0006418
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0006378	abnormal spermatogonia morphology	CCO:MP0006378
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0006362	abnormal male germ cell morphology	CCO:MP0006362
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0002786	abnormal Leydig cell morphology	CCO:MP0002786
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0003045	fibrosis	CCO:MP0003045
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0002780	decreased circulating testosterone level	CCO:MP0002780
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0002784	abnormal Sertoli cell morphology	CCO:MP0002784
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0002789	male pseudohermaphroditism	CCO:MP0002789
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0005189	abnormal anogenital distance	CCO:MP0005189
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0005536	Leydig cell hypoplasia	CCO:MP0005536
MGI:94891	Dhh	Dhh<tm1Amc>/Dhh<tm1Amc>	involves: 129S1/Sv * C57BL/6J * Swiss Webster	MP:0001751	increased circulating luteinizing hormone level	CCO:MP0001751
MGI:2183453	Dlgap5	Dlgap5<tm1Tfts>/Dlgap5<tm1Tfts>	involves: 129S7/SvEvBrd	MP:0001926	female infertility	CCO:MP0001926
MGI:2183453	Dlgap5	Dlgap5<tm1Tfts>/Dlgap5<tm1Tfts>	involves: 129S7/SvEvBrd	MP:0003845	abnormal decidualization	CCO:MP0003845
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0001926	female infertility	CCO:MP0001926
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C57BL/6J	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<+>	involves: 129S4/SvJae * C57BL/6J	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0001931	abnormal oogenesis	CCO:MP0001931
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0004805	absent oocytes	CCO:MP0004805
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0001932	abnormal spermiogenesis	CCO:MP0001932
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0004856	decreased ovary weight	CCO:MP0004856
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0005159	azoospermia	CCO:MP0005159
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0001926	female infertility	CCO:MP0001926
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:105393	Dmc1	Dmc1<Mei11>/Dmc1<Mei11>	involves: 129S4/SvJae * C57BL/6J	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0001924	infertility	CCO:MP0001924
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004805	absent oocytes	CCO:MP0004805
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001127	small ovary	CCO:MP0001127
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001924	infertility	CCO:MP0001924
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001931	abnormal oogenesis	CCO:MP0001931
MGI:105393	Dmc1	Dmc1<tm1Tkm>/Dmc1<tm1Tkm>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:105393	Dmc1	Dmc1<tm1Jcs>/Dmc1<tm1Jcs>	involves: 129S4/SvJae * C57BL/6J	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0000516	abnormal urinary system morphology	CCO:MP0000516
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0001513	limb grasping	CCO:MP0001513
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0002064	seizures	CCO:MP0002064
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0000539	distended urinary bladder	CCO:MP0000539
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0009546	absent gastric milk in neonates	CCO:MP0009546
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<+>	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Tg(IghMyc)22Bri/0"	involves: 129/Sv * C57BL * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0002059	abnormal seminal gland morphology	CCO:MP0002059
MGI:1344415	Dmtf1	Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>	involves: 129/Sv * C57BL/6	MP:0002444	abnormal T cell physiology	CCO:MP0002444
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000858	altered metastatic potential	CCO:MP0000858
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0008000	ovary tumor	CCO:MP0008000
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0008014	lung tumor	CCO:MP0008014
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0008014	lung tumor	CCO:MP0008014
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000858	altered metastatic potential	CCO:MP0000858
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0008014	lung tumor	CCO:MP0008014
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0008014	lung tumor	CCO:MP0008014
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000858	altered metastatic potential	CCO:MP0000858
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<tm1Cjs>,Kras<tm3Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0003580	fibroma	CCO:MP0003580
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:1344415	Dmtf1	"Dmtf1<tm1Cjs>/Dmtf1<+>,Kras<tm2Tyj>/Kras<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	C3HeB/FeJ-Dst<dt-J>	MP:0001527	athetotic walking movements	CCO:MP0001527
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	C3HeB/FeJ-Dst<dt-J>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104627	Dst	Dst<dt-35J>/Dst<dt-35J>	involves: 129S4/SvJae * C57BL/6	MP:0002066	abnormal motor capabilities/coordination/movement	CCO:MP0002066
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	C3HeB/FeJ-Dst<dt-J>	MP:0001504	abnormal posture	CCO:MP0001504
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	C3HeB/FeJ-Dst<dt-J>	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:104627	Dst	Dst<dt-32J>/Dst<dt-32J>	involves: 129S/Sv * 129S2/SvPas	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104627	Dst	Dst<dt>/Dst<dt>	Q-Dst<dt>	MP:0003225	axonal dystrophy	CCO:MP0003225
MGI:104627	Dst	Dst<dt-alb>/Dst<dt-alb>	BALB/cByJ-Dst<dt-alb>	MP:0005323	dystonia	CCO:MP0005323
MGI:104627	Dst	Dst<dt-alb>/Dst<dt-alb>	BALB/cByJ-Dst<dt-alb>	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0003871	abnormal myelin sheath morphology	CCO:MP0003871
MGI:104627	Dst	Dst<dt>/Dst<dt>	Q-Dst<dt>	MP:0000754	paresis	CCO:MP0000754
MGI:104627	Dst	Dst<dt>/Dst<dt>	Q-Dst<dt>	MP:0002229	neurodegeneration	CCO:MP0002229
MGI:104627	Dst	Dst<dt>/Dst<dt>	Q-Dst<dt>	MP:0002183	gliosis	CCO:MP0002183
MGI:104627	Dst	Dst<dt-32J>/Dst<dt-32J>	involves: 129S/Sv * 129S2/SvPas	MP:0003281	fecal incontinence	CCO:MP0003281
MGI:104627	Dst	Dst<dt>/Dst<dt>	Q-Dst<dt>	MP:0003045	fibrosis	CCO:MP0003045
MGI:104627	Dst	Dst<dt-alb>/Dst<dt-alb>	BALB/cByJ-Dst<dt-alb>	MP:0002882	abnormal neuron morphology	CCO:MP0002882
MGI:104627	Dst	Dst<dt>/Dst<dt>	involves: Q	MP:0002083	premature death	CCO:MP0002083
MGI:104627	Dst	Dst<dt>/Dst<dt>	involves: Q	MP:0001513	limb grasping	CCO:MP0001513
MGI:104627	Dst	Dst<dt>/Dst<dt>	involves: Q	MP:0001524	impaired limb coordination	CCO:MP0001524
MGI:104627	Dst	Dst<dt>/Dst<dt>	involves: Q	MP:0002229	neurodegeneration	CCO:MP0002229
MGI:104627	Dst	Dst<dt>/Dst<dt>	involves: Q	MP:0005323	dystonia	CCO:MP0005323
MGI:104627	Dst	Dst<dt>/Dst<dt>	involves: C57BL/6 * Q	MP:0000921	demyelination	CCO:MP0000921
MGI:104627	Dst	Dst<dt>/Dst<dt>	Q-Dst<dt>	MP:0005323	dystonia	CCO:MP0005323
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0002269	muscular atrophy	CCO:MP0002269
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0001523	impaired righting response	CCO:MP0001523
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0000414	alopecia	CCO:MP0000414
MGI:104627	Dst	Dst<dt>/Dst<dt>	Q-Dst<dt>	MP:0002083	premature death	CCO:MP0002083
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0001208	blistering	CCO:MP0001208
MGI:104627	Dst	Dst<dt-32J>/Dst<dt-32J>	involves: 129S/Sv * 129S2/SvPas	MP:0003280	urinary incontinence	CCO:MP0003280
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0005323	dystonia	CCO:MP0005323
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0005405	axon degeneration	CCO:MP0005405
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0002908	delayed wound healing	CCO:MP0002908
MGI:104627	Dst	Dst<dt-24J>/Dst<dt-24J>	involves: C57BL/6	MP:0003225	axonal dystrophy	CCO:MP0003225
MGI:104627	Dst	Dst<dt-32J>/Dst<dt-32J>	involves: 129S/Sv * 129S2/SvPas	MP:0001513	limb grasping	CCO:MP0001513
MGI:104627	Dst	Dst<dt-32J>/Dst<dt-32J>	involves: 129S/Sv * 129S2/SvPas	MP:0002752	abnormal somatic nervous system morphology	CCO:MP0002752
MGI:104627	Dst	Dst<tm1Efu>/Dst<tm1Efu>	involves: C57BL/6	MP:0000585	kinked tail	CCO:MP0000585
MGI:104627	Dst	Dst<dt-30J>/Dst<dt-30J>	C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:104627	Dst	Dst<dt-31J>/Dst<dt-31J>	DBA/1LacJ	MP:0005323	dystonia	CCO:MP0005323
MGI:104627	Dst	Dst<dt-31J>/Dst<dt-31J>	DBA/1LacJ	MP:0002083	premature death	CCO:MP0002083
MGI:104627	Dst	Dst<dt-30J>/Dst<dt-30J>	C57BL/6J	MP:0002229	neurodegeneration	CCO:MP0002229
MGI:104627	Dst	Dst<dt-30J>/Dst<dt-30J>	C57BL/6J	MP:0005323	dystonia	CCO:MP0005323
MGI:104627	Dst	Dst<dt-33J>/Dst<dt-33J>	129S1/Sv	MP:0001405	impaired coordination	CCO:MP0001405
MGI:104627	Dst	Dst<dt-33J>/Dst<dt-33J>	129S1/Sv	MP:0001393	ataxia	CCO:MP0001393
MGI:104627	Dst	Dst<dt-33J>/Dst<dt-33J>	129S1/Sv	MP:0002064	seizures	CCO:MP0002064
MGI:104627	Dst	Dst<dt-33J>/Dst<dt-33J>	129S1/Sv	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104627	Dst	Dst<dt-36J>/Dst<dt-36J>	C57BL/6J-Dst<dt-36J>/J	MP:0001504	abnormal posture	CCO:MP0001504
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0003871	abnormal myelin sheath morphology	CCO:MP0003871
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0003994	abnormal dorsal spinal root morphology	CCO:MP0003994
MGI:104627	Dst	Dst<dt-38J>/Dst<dt-38J>	involves: BALB/cByJ * C57BL/6J	MP:0001504	abnormal posture	CCO:MP0001504
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0003633	abnormal nervous system physiology	CCO:MP0003633
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0000965	abnormal sensory neuron morphology	CCO:MP0000965
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:104627	Dst	Dst<dt-38J>/Dst<dt-38J>	involves: BALB/cByJ * C57BL/6J	MP:0000743	muscle spasm	CCO:MP0000743
MGI:104627	Dst	Dst<dt-38J>/Dst<dt-38J>	involves: BALB/cByJ * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0000958	peripheral nervous system degeneration	CCO:MP0000958
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0001524	impaired limb coordination	CCO:MP0001524
MGI:104627	Dst	Dst<Tg4>/Dst<Tg4>	involves: CD-1	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104627	Dst	Dst<dt-38J>/Dst<dt-38J>	involves: BALB/cByJ * C57BL/6J	MP:0000747	muscle weakness	CCO:MP0000747
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0002095	abnormal skin pigmentation	CCO:MP0002095
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0005316	abnormal response to tactile stimuli	CCO:MP0005316
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0001299	abnormal eye distance/ position	CCO:MP0001299
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0001489	decreased startle reflex	CCO:MP0001489
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0001525	impaired balance	CCO:MP0001525
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0001405	impaired coordination	CCO:MP0001405
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0001393	ataxia	CCO:MP0001393
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0000745	tremors	CCO:MP0000745
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0002752	abnormal somatic nervous system morphology	CCO:MP0002752
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0001504	abnormal posture	CCO:MP0001504
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0005656	decreased aggression	CCO:MP0005656
MGI:104627	Dst	Dst<dt-37J>/Dst<dt-37J>	C57BL/6J-Dst<dt-37J>/J	MP:0009400	decreased skeletal muscle fiber size	CCO:MP0009400
MGI:104627	Dst	Dst<dt-37J>/Dst<dt-37J>	C57BL/6J-Dst<dt-37J>/J	MP:0003225	axonal dystrophy	CCO:MP0003225
MGI:104627	Dst	Dst<dt-37J>/Dst<dt-37J>	C57BL/6J-Dst<dt-37J>/J	MP:0002883	chromatolysis	CCO:MP0002883
MGI:104627	Dst	Dst<dt-37J>/Dst<dt-37J>	C57BL/6J-Dst<dt-37J>/J	MP:0005323	dystonia	CCO:MP0005323
MGI:104627	Dst	Dst<dt-37J>/Dst<dt-37J>	C57BL/6J-Dst<dt-37J>/J	MP:0000921	demyelination	CCO:MP0000921
MGI:104627	Dst	Dst<dt-37J>/Dst<dt-37J>	C57BL/6J-Dst<dt-37J>/J	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:104627	Dst	Dst<dt-37J>/Dst<dt-37J>	C57BL/6J-Dst<dt-37J>/J	MP:0001523	impaired righting response	CCO:MP0001523
MGI:104627	Dst	Dst<dt-37J>/Dst<dt-37J>	C57BL/6J-Dst<dt-37J>/J	MP:0001265	decreased body size	CCO:MP0001265
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0003994	abnormal dorsal spinal root morphology	CCO:MP0003994
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0000958	peripheral nervous system degeneration	CCO:MP0000958
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0000921	demyelination	CCO:MP0000921
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0000965	abnormal sensory neuron morphology	CCO:MP0000965
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0005405	axon degeneration	CCO:MP0005405
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0005356	positive geotaxis	CCO:MP0005356
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0003871	abnormal myelin sheath morphology	CCO:MP0003871
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0002980	abnormal postural reflex	CCO:MP0002980
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0004768	abnormal axonal transport	CCO:MP0004768
MGI:104627	Dst	Dst<dt-27J>/Dst<+>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:104627	Dst	Dst<dt-27J>/Dst<+>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:104627	Dst	Dst<dt-27J>/Dst<+>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:104627	Dst	Dst<Tg4>/Dst<+>	involves: CD-1	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:104627	Dst	Dst<Tg4>/Dst<+>	involves: CD-1	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:104627	Dst	Dst<Tg4>/Dst<+>	involves: CD-1	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:104627	Dst	Dst<dt-J>/Dst<dt-J>	B6C3Fe a/a-Dst<dt-J>/J	MP:0006198	enophthalmos	CCO:MP0006198
MGI:104627	Dst	Dst<dt-23J>/Dst<dt-23J>	Not Specified	MP:0003225	axonal dystrophy	CCO:MP0003225
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0003633	abnormal nervous system physiology	CCO:MP0003633
MGI:104627	Dst	Dst<dt-27J>/Dst<dt-27J>	B10.PL/(73NS)Sn-Dst<dt-27J>/J	MP:0002651	abnormal sciatic nerve	CCO:MP0002651
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0002419	abnormal innate immunity	CCO:MP0002419
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0008577	increased circulating interferon-gamma level	CCO:MP0008577
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0008593	increased circulating interleukin-10 level	CCO:MP0008593
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0008596	increased circulating interleukin-6 level	CCO:MP0008596
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0008721	abnormal chemokine level	CCO:MP0008721
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0008735	increased susceptibility to endotoxin shock	CCO:MP0008735
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0008751	abnormal interleukin level	CCO:MP0008751
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0003724	increased susceptibility to induced arthritis	CCO:MP0003724
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0002516	abnormal PGE2 physiology	CCO:MP0002516
MGI:105120	Dusp1	Dusp1<tm1Lex>/Dusp1<tm1Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0008553	increased circulating tumor necrosis factor level	CCO:MP0008553
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0001861	lung inflammation	CCO:MP0001861
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0001179	thick alveolar septum	CCO:MP0001179
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0001596	hypotension	CCO:MP0001596
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0003957	abnormal nitric oxide homeostasis	CCO:MP0003957
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0003009	abnormal cytokine secretion	CCO:MP0003009
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0003828	pulmonary edema	CCO:MP0003828
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0006264	decreased systolic blood pressure	CCO:MP0006264
MGI:105120	Dusp1	Dusp1<tm1Brv>/Dusp1<tm1Brv>	involves: 129S2/SvPas	MP:0001573	abnormal circulating alanine transaminase level	CCO:MP0001573
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0004974	decreased regulatory T cell number	CCO:MP0004974
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0004803	increased susceptibility to autoimmune diabetes	CCO:MP0004803
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0004955	increased thymus weight	CCO:MP0004955
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0008074	increased CD4-positive T cell number	CCO:MP0008074
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0008078	increased CD8-positive T cell number	CCO:MP0008078
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	involves: 129S4/SvJae * C57BL/6	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0002432	abnormal CD4-positive T cell morphology	CCO:MP0002432
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0000623	decreased salivation	CCO:MP0000623
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	involves: 129S4/SvJae * C57BL/6	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Phactr4<humdy>/Phactr4<humdy>"	involves: 129S4/SvJae * C57BL/6J	MP:0000914	exencephaly	CCO:MP0000914
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0000714	increased thymocyte number	CCO:MP0000714
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0008699	increased interleukin-4 secretion	CCO:MP0008699
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0002408	abnormal double-positive T cell morphology	CCO:MP0002408
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0005015	increased T cell number	CCO:MP0005015
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0005010	abnormal CD8-positive T cell morphology	CCO:MP0005010
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0001870	salivary gland inflammation	CCO:MP0001870
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008515	thin retinal outer nuclear layer	CCO:MP0008515
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<+>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0005240	abnormal amacrine cell morphology	CCO:MP0005240
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0008566	increased interferon-gamma secretion	CCO:MP0008566
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	NOD.Cg-E2f1<tm1Meg>	MP:0004031	insulitis	CCO:MP0004031
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0003734	abnormal retinal inner plexiform layer morphology	CCO:MP0003734
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0000714	increased thymocyte number	CCO:MP0000714
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0002408	abnormal double-positive T cell morphology	CCO:MP0002408
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006071	abnormal retinal progenitor morphology	CCO:MP0006071
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0004022	abnormal cone electrophysiology	CCO:MP0004022
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0000623	decreased salivation	CCO:MP0000623
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<+>,Phactr4<humdy>/Phactr4<humdy>"	involves: 129S4/SvJae * C57BL/6J	MP:0000914	exencephaly	CCO:MP0000914
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008515	thin retinal outer nuclear layer	CCO:MP0008515
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6)	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:101941	E2f1	E2f1<tm1Meg>/E2f1<tm1Meg>	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0004022	abnormal cone electrophysiology	CCO:MP0004022
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm4Gle>/E2f3<tm4Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0005668	decreased circulating leptin level	CCO:MP0005668
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002644	decreased circulating triglyceride level	CCO:MP0002644
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm5(E2f1)Gle>/E2f3<tm5(E2f1)Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0005120	decreased circulating growth hormone level	CCO:MP0005120
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0000771	abnormal brain size	CCO:MP0000771
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0008288	abnormal adrenal cortex morphology	CCO:MP0008288
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002679	abnormal corpus luteum	CCO:MP0002679
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0006395	abnormal epiphyseal plate morphology	CCO:MP0006395
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0004701	decreased circulating insulin-like growth factor I level	CCO:MP0004701
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0006382	abnormal lung epithelium morphology	CCO:MP0006382
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0005158	ovary hypoplasia	CCO:MP0005158
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001783	decreased white adipose tissue amount	CCO:MP0001783
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001926	female infertility	CCO:MP0001926
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001265	decreased body size	CCO:MP0001265
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002083	premature death	CCO:MP0002083
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001940	testicular hypoplasia	CCO:MP0001940
MGI:101941	E2f1	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001925	male infertility	CCO:MP0001925
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0000163	abnormal cartilage morphology	CCO:MP0000163
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0004185	abnormal adipocyte glucose uptake	CCO:MP0004185
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<+>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0003055	abnormal long bone epiphyseal plate morphology	CCO:MP0003055
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0003452	abnormal parotid gland morphology	CCO:MP0003452
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0003793	abnormal submandibular gland morphology	CCO:MP0003793
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm1Lees>/E2f3<tm1Lees>"	involves: 129S2/SvPas	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0008716	lung non-small cell carcinoma	CCO:MP0008716
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<tm1Tyj>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0001944	abnormal pancreas morphology	CCO:MP0001944
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002727	decreased circulating insulin level	CCO:MP0002727
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002786	abnormal Leydig cell morphology	CCO:MP0002786
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S2/SvPas * 129S7/SvEvBrd * SKH1	MP:0001203	increased sensitivity to skin irradiation	CCO:MP0001203
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0003496	thyroid adenoma	CCO:MP0003496
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0004898	uterine hemorrhage	CCO:MP0004898
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<+>,E2f3<tm1Lees>/E2f3<tm1Lees>"	involves: 129S2/SvPas	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0001560	abnormal circulating insulin level	CCO:MP0001560
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm1Lees>/E2f3<+>"	involves: 129S2/SvPas	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm1Lees>/E2f3<+>"	involves: 129S2/SvPas	MP:0008489	postnatal slow weight gain	CCO:MP0008489
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * SKH1	MP:0001203	increased sensitivity to skin irradiation	CCO:MP0001203
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0005220	abnormal exocrine pancreas morphology	CCO:MP0005220
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0005217	abnormal pancreatic beta cell morphology	CCO:MP0005217
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0005293	impaired glucose tolerance	CCO:MP0005293
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0005454	decreased adipose tissue amount	CCO:MP0005454
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002891	increased insulin sensitivity	CCO:MP0002891
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0003059	decreased insulin secretion	CCO:MP0003059
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0008301	adrenal medulla hyperplasia	CCO:MP0008301
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002947	hemangioma	CCO:MP0002947
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<+>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0002163	abnormal gland morphology	CCO:MP0002163
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0000681	abnormal thyroid gland morphology	CCO:MP0000681
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0009321	histiocytic sarcoma	CCO:MP0009321
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<+>,Rb1<tm1Tyj>/Rb1<tm1Tyj>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<+>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0003496	thyroid adenoma	CCO:MP0003496
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0009172	small pancreatic islets	CCO:MP0009172
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0009168	decreased pancreatic islet number	CCO:MP0009168
MGI:101941	E2f1	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm3Lees>/E2f3<tm3Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0009109	decreased pancreas weight	CCO:MP0009109
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0000003	abnormal adipose tissue morphology	CCO:MP0000003
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0001346	abnormal lacrimal gland morphology	CCO:MP0001346
MGI:101941	E2f1	E2f1<tm1Njd>/E2f1<tm1Njd>	involves: 129S2/SvPas * C57BL/6	MP:0000613	abnormal salivary gland morphology	CCO:MP0000613
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0005350	increased susceptibility to autoimmune disorder	CCO:MP0005350
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0008078	increased CD8-positive T cell number	CCO:MP0008078
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008453	decreased retinal rod cell number	CCO:MP0008453
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0005350	increased susceptibility to autoimmune disorder	CCO:MP0005350
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0002083	premature death	CCO:MP0002083
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0004952	increased spleen weight	CCO:MP0004952
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0008049	increased memory T cell number	CCO:MP0008049
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0001790	abnormal immune system physiology	CCO:MP0001790
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0000685	abnormal immune system morphology	CCO:MP0000685
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0003944	abnormal T cell subpopulation ratio	CCO:MP0003944
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Tg(TcraH-Y,TcrbH-Y)71Vbo/?"	involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0000685	abnormal immune system morphology	CCO:MP0000685
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0002096	abnormal skin condition/ morphology	CCO:MP0002096
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0001190	reddish skin	CCO:MP0001190
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0000415	partial hair loss	CCO:MP0000415
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0001860	liver inflammation	CCO:MP0001860
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0002357	abnormal spleen white pulp morphology	CCO:MP0002357
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0001861	lung inflammation	CCO:MP0001861
MGI:1096341	E2f2	E2f2<tm1Zubi>/E2f2<tm1Zubi>	involves: 129S1/Sv * C57BL/6	MP:0001790	abnormal immune system physiology	CCO:MP0001790
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1096341	E2f2	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1096341	E2f2	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1096341	E2f2	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096341	E2f2	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1096341	E2f2	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096340	E2f3	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:1096340	E2f3	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001855	atrial thrombosis	CCO:MP0001855
MGI:1096340	E2f3	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0005240	abnormal amacrine cell morphology	CCO:MP0005240
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0000420	ruffled hair	CCO:MP0000420
MGI:1096340	E2f3	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008453	decreased retinal rod cell number	CCO:MP0008453
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0005048	thrombosis	CCO:MP0005048
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0006138	congestive heart failure	CCO:MP0006138
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001861	lung inflammation	CCO:MP0001861
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0003828	pulmonary edema	CCO:MP0003828
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0008489	postnatal slow weight gain	CCO:MP0008489
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0009431	decreased fetal weight	CCO:MP0009431
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<+>	involves: 129S2/SvPas * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1096340	E2f3	E2f3<tm1.2Gle>/E2f3<tm1.2Gle>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096340	E2f3	E2f3<tm1.2Gle>/E2f3<tm1.2Gle>	involves: 129P2/OlaHsd * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1096340	E2f3	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0005668	decreased circulating leptin level	CCO:MP0005668
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001940	testicular hypoplasia	CCO:MP0001940
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0004701	decreased circulating insulin-like growth factor I level	CCO:MP0004701
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002644	decreased circulating triglyceride level	CCO:MP0002644
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0005158	ovary hypoplasia	CCO:MP0005158
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0005120	decreased circulating growth hormone level	CCO:MP0005120
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001783	decreased white adipose tissue amount	CCO:MP0001783
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002679	abnormal corpus luteum	CCO:MP0002679
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002083	premature death	CCO:MP0002083
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0000771	abnormal brain size	CCO:MP0000771
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001265	decreased body size	CCO:MP0001265
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001925	male infertility	CCO:MP0001925
MGI:1096340	E2f3	E2f3<tm2.1Gle>/E2f3<tm2.1Gle>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001783	decreased white adipose tissue amount	CCO:MP0001783
MGI:1096340	E2f3	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm5(E2f1)Gle>/E2f3<tm5(E2f1)Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1096340	E2f3	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm3.1Gle>/E2f3<tm3.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1096340	E2f3	E2f3<tm1.1Gle>/E2f3<tm1.1Gle>	129-E2f3<tm1.1Gle>	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm4Gle>/E2f3<tm4Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0006382	abnormal lung epithelium morphology	CCO:MP0006382
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0008288	abnormal adrenal cortex morphology	CCO:MP0008288
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0006395	abnormal epiphyseal plate morphology	CCO:MP0006395
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f2<tm1Zubi>/E2f2<tm1Zubi>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129 * FVB/N * NIH Black Swiss	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1096340	E2f3	E2f3<tm1.1Gle>/E2f3<tm1.1Gle>	B6.129P2-E2f3<tm1.1Gle>	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1096340	E2f3	"E2f1<tm1Meg>/E2f1<tm1Meg>,E2f3<tm2.1Gle>/E2f3<tm2.1Gle>"	involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001926	female infertility	CCO:MP0001926
MGI:1096340	E2f3	E2f3<tm1.1Gle>/E2f3<tm1.1Gle>	FVB.129P2-E2f3<tm1.1Gle>	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0003055	abnormal long bone epiphyseal plate morphology	CCO:MP0003055
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:1096340	E2f3	E2f3<tm2Lees>/E2f3<tm2Lees>	either: 129S/Sv-E2f3<tm2Lees> or (involves: 129S4/SvJae * C57BL/6)	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm1Lees>/E2f3<+>"	involves: 129S2/SvPas	MP:0008489	postnatal slow weight gain	CCO:MP0008489
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm1Lees>/E2f3<+>"	involves: 129S2/SvPas	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<+>,E2f3<tm1Lees>/E2f3<tm1Lees>"	involves: 129S2/SvPas	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1096340	E2f3	E2f3<tm1Lees>/E2f3<tm1Lees>	involves: 129S2/SvPas	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0000163	abnormal cartilage morphology	CCO:MP0000163
MGI:1096340	E2f3	E2f3<tm3Lees>/E2f3<tm3Lees>	either: 129S/Sv-E2f3<tm3Lees> or (involves: 129S4/SvJae * C57BL/6)	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm2Lees>/E2f3<tm2Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1096340	E2f3	E2f3<tm2Lees>/E2f3<tm2Lees>	either: 129S/Sv-E2f3<tm2Lees> or (involves: 129S4/SvJae * C57BL/6)	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm3Lees>/E2f3<tm3Lees>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1096340	E2f3	"E2f1<tm1Njd>/E2f1<tm1Njd>,E2f3<tm1Lees>/E2f3<tm1Lees>"	involves: 129S2/SvPas	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000248	macrocytosis	CCO:MP0000248
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001400	hyperresponsive	CCO:MP0001400
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0003449	abnormal intestinal goblet cells	CCO:MP0003449
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001529	abnormal vocalization	CCO:MP0001529
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001209	spontaneous skin ulceration	CCO:MP0001209
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000490	abnormal crypts of Lieberkuhn morphology	CCO:MP0000490
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000488	abnormal intestinal epithelium morphology	CCO:MP0000488
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0008044	increased NK cell number	CCO:MP0008044
MGI:103012	E2f4	"E2f4<tm1Jrn>/E2f4<tm1Jrn>,E2f5<tm1Dli>/E2f5<tm1Dli>"	involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:103012	E2f4	"E2f4<tm1Jrn>/E2f4<tm1Jrn>,E2f5<tm1Dli>/E2f5<tm1Dli>"	involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0008142	decreased small intestinal villus size	CCO:MP0008142
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001921	reduced fertility	CCO:MP0001921
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0002424	abnormal reticulocyte morphology	CCO:MP0002424
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000445	short snout	CCO:MP0000445
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000334	decreased granulocyte number	CCO:MP0000334
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000346	broad head	CCO:MP0000346
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0002441	abnormal granulocyte morphology	CCO:MP0002441
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0000511	abnormal intestinal mucosa morphology	CCO:MP0000511
MGI:103012	E2f4	E2f4<tm1Jrn>/E2f4<tm1Jrn>	involves: 129P2/OlaHsd * C57BL/6	MP:0008108	abnormal small intestinal villus morphology	CCO:MP0008108
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0000248	macrocytosis	CCO:MP0000248
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002416	abnormal proerythroblast morphology	CCO:MP0002416
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002124	abnormal red blood cell	CCO:MP0002124
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002642	anisocytosis	CCO:MP0002642
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0005449	abnormal food intake	CCO:MP0005449
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0008789	abnormal olfactory epithelium morphology	CCO:MP0008789
MGI:103012	E2f4	"E2f4<tm1Lees>/E2f4<tm1Lees>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002424	abnormal reticulocyte morphology	CCO:MP0002424
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:103012	E2f4	"E2f4<tm1Lees>/E2f4<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002412	increased susceptibility to bacterial infection	CCO:MP0002412
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002244	abnormal turbinate morphology	CCO:MP0002244
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002237	abnormal nasal cavity morphology	CCO:MP0002237
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0000445	short snout	CCO:MP0000445
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001529	abnormal vocalization	CCO:MP0001529
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001429	dehydration	CCO:MP0001429
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001867	rhinitis	CCO:MP0001867
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0000049	abnormal middle ear morphology	CCO:MP0000049
MGI:103012	E2f4	E2f4<tm1Lees>/E2f4<tm1Lees>	involves: 129S2/SvPas * C57BL/6	MP:0001850	increased susceptibility to otitis media	CCO:MP0001850
MGI:103012	E2f4	"E2f4<tm1Lees>/E2f4<tm1Lees>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:103012	E2f4	"E2f4<tm1Lees>/E2f4<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:103012	E2f4	"E2f4<tm1Lees>/E2f4<tm1Lees>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002406	increased susceptibility to infection	CCO:MP0002406
MGI:105091	E2f5	"E2f4<tm1Jrn>/E2f4<tm1Jrn>,E2f5<tm1Dli>/E2f5<tm1Dli>"	involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:105091	E2f5	"E2f4<tm1Jrn>/E2f4<tm1Jrn>,E2f5<tm1Dli>/E2f5<tm1Dli>"	involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0001916	intracerebral hemorrhage	CCO:MP0001916
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0000074	abnormal neurocranium morphology	CCO:MP0000074
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0001893	non-obstructive hydrocephaly	CCO:MP0001893
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0000076	abnormal calvaria morphology	CCO:MP0000076
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0002200	abnormal brain ventricle/choroid plexus morphology	CCO:MP0002200
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0000820	abnormal choroid plexus morphology	CCO:MP0000820
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0000825	dilated lateral ventricles	CCO:MP0000825
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0000827	dilated third ventricle	CCO:MP0000827
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0002653	abnormal ependyma morphology	CCO:MP0002653
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0001917	intraventricular hemorrhage	CCO:MP0001917
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0001393	ataxia	CCO:MP0001393
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0001429	dehydration	CCO:MP0001429
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:105091	E2f5	E2f5<tm1Dli>/E2f5<tm1Dli>	either: (involves: 129S1/Sv * BALB/c) or (involves: 129S1/Sv * C57BL/6)	MP:0000420	ruffled hair	CCO:MP0000420
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<+>,E2f6<tm1Lees>/E2f6<+>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004615	cervical vertebral transformation	CCO:MP0004615
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004616	lumbar vertebral transformation	CCO:MP0004616
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004618	thoracic vertebral transformation	CCO:MP0004618
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<+>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004615	cervical vertebral transformation	CCO:MP0004615
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0000237	decreased blood cell number	CCO:MP0000237
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<+>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004618	thoracic vertebral transformation	CCO:MP0004618
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<+>,E2f6<tm1Lees>/E2f6<+>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004616	lumbar vertebral transformation	CCO:MP0004616
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<+>,E2f6<tm1Lees>/E2f6<+>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004618	thoracic vertebral transformation	CCO:MP0004618
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<+>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<+>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004615	cervical vertebral transformation	CCO:MP0004615
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<+>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004616	lumbar vertebral transformation	CCO:MP0004616
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<+>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004618	thoracic vertebral transformation	CCO:MP0004618
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<+>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004616	lumbar vertebral transformation	CCO:MP0004616
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:1354159	E2f6	E2f6<tm1Lees>/E2f6<+>	involves: 129S4/SvJae * C57BL/6	MP:0004618	thoracic vertebral transformation	CCO:MP0004618
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1354159	E2f6	E2f6<tm1Lees>/E2f6<tm1Lees>	involves: 129S4/SvJae * C57BL/6	MP:0004618	thoracic vertebral transformation	CCO:MP0004618
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0001393	ataxia	CCO:MP0001393
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0004615	cervical vertebral transformation	CCO:MP0004615
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1354159	E2f6	E2f6<tm1Lees>/E2f6<tm1Lees>	involves: 129S4/SvJae * C57BL/6	MP:0004616	lumbar vertebral transformation	CCO:MP0004616
MGI:1354159	E2f6	E2f6<tm1Lees>/E2f6<tm1Lees>	involves: 129S4/SvJae * C57BL/6	MP:0004615	cervical vertebral transformation	CCO:MP0004615
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0000851	cerebellum hypoplasia	CCO:MP0000851
MGI:1354159	E2f6	E2f6<tm1Lees>/E2f6<+>	involves: 129S4/SvJae * C57BL/6	MP:0004616	lumbar vertebral transformation	CCO:MP0004616
MGI:1354159	E2f6	"Bmi1<tm1Brn>/Bmi1<tm1Brn>,E2f6<tm1Lees>/E2f6<tm1Lees>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:1354159	E2f6	E2f6<tm1Sgau>/E2f6<tm1Sgau>	involves: 129S4/SvJae * C57BL/6	MP:0001152	Leydig cell hyperplasia	CCO:MP0001152
MGI:1354159	E2f6	E2f6<tm1Sgau>/E2f6<tm1Sgau>	involves: 129S4/SvJae * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1354159	E2f6	E2f6<tm1Sgau>/E2f6<tm1Sgau>	involves: 129S4/SvJae * C57BL/6	MP:0004616	lumbar vertebral transformation	CCO:MP0004616
MGI:1354159	E2f6	E2f6<tm1Sgau>/E2f6<tm1Sgau>	involves: 129S4/SvJae * C57BL/6	MP:0004618	thoracic vertebral transformation	CCO:MP0004618
MGI:1354159	E2f6	E2f6<tm1Sgau>/E2f6<+>	involves: 129S4/SvJae * C57BL/6	MP:0004616	lumbar vertebral transformation	CCO:MP0004616
MGI:1354159	E2f6	E2f6<tm1Hgmr>/E2f6<tm1Hgmr>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1289147	E2f7	E2f7<tm1.1Gle>/E2f7<tm1.1Gle>	involves: 129S6/SvEvTac * FVB/N	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<+>"	involves: 129S6/SvEvTac * FVB/N	MP:0001265	decreased body size	CCO:MP0001265
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<+>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1289147	E2f7	"E2f7<tm1Gle>/E2f7<tm1Gle>,E2f8<tm1Gle>/E2f8<tm1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0008402	increased cellular sensitivity to alkylating agents	CCO:MP0008402
MGI:1289147	E2f7	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<+>"	involves: 129S6/SvEvTac * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:1922038	E2f8	"E2f7<tm1Gle>/E2f7<tm1Gle>,E2f8<tm1Gle>/E2f8<tm1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0008402	increased cellular sensitivity to alkylating agents	CCO:MP0008402
MGI:1922038	E2f8	E2f8<tm1.1Gle>/E2f8<tm1.1Gle>	involves: 129S6/SvEvTac * FVB/N	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<+>"	involves: 129S6/SvEvTac * FVB/N	MP:0001265	decreased body size	CCO:MP0001265
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<+>"	involves: 129S6/SvEvTac * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<tm1.1Gle>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1922038	E2f8	"E2f7<tm1.1Gle>/E2f7<+>,E2f8<tm1.1Gle>/E2f8<tm1.1Gle>"	involves: 129S6/SvEvTac * FVB/N	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:109530	E4f1	E4f1<tm1Pisc>/E4f1<tm1Pisc>	involves: 129S4/SvJae * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:109530	E4f1	E4f1<tm1Pisc>/E4f1<tm1Pisc>	involves: 129S4/SvJae * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:109530	E4f1	E4f1<tm1Pisc>/E4f1<tm1Pisc>	involves: 129S4/SvJae * C57BL/6	MP:0001674	abnormal triploblastic development	CCO:MP0001674
MGI:109530	E4f1	E4f1<tm1Pisc>/E4f1<tm1Pisc>	involves: 129S4/SvJae * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:109530	E4f1	E4f1<tm1Pisc>/E4f1<tm1Pisc>	involves: 129S4/SvJae * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005159	azoospermia	CCO:MP0005159
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001925	male infertility	CCO:MP0001925
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001926	female infertility	CCO:MP0001926
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001935	decreased litter size	CCO:MP0001935
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001147	small testis	CCO:MP0001147
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:2148922	Ehmt2	"Alpl<tm1(cre)Nagy>/Alpl<+>,Ehmt2<tm2Yshk>/Ehmt2<tm2.1Yshk>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:2148922	Ehmt2	Ehmt2<Gt(ES62)Feil>/Ehmt2<Gt(ES62)Feil>	involves: 129P2/OlaHsd * C57BL/6	MP:0001713	decreased trophoblast giant cell number	CCO:MP0001713
MGI:2148922	Ehmt2	Ehmt2<Gt(ES62)Feil>/Ehmt2<Gt(ES62)Feil>	involves: 129P2/OlaHsd * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:2148922	Ehmt2	Ehmt2<Gt(ES62)Feil>/Ehmt2<Gt(ES62)Feil>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2148922	Ehmt2	Ehmt2<Gt(ES62)Feil>/Ehmt2<Gt(ES62)Feil>	involves: 129P2/OlaHsd * C57BL/6	MP:0003787	abnormal imprinting	CCO:MP0003787
MGI:2148922	Ehmt2	Ehmt2<Gt(ES62)Feil>/Ehmt2<Gt(ES62)Feil>	involves: 129P2/OlaHsd * C57BL/6	MP:0000929	open neural tube	CCO:MP0000929
MGI:2148922	Ehmt2	Ehmt2<Gt(ES62)Feil>/Ehmt2<Gt(ES62)Feil>	involves: 129P2/OlaHsd * C57BL/6	MP:0004259	small placenta	CCO:MP0004259
MGI:2148922	Ehmt2	Ehmt2<tm1Yshk>/Ehmt2<tm1Yshk>	involves: C57BL/6 * CBA	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:2148922	Ehmt2	Ehmt2<tm1Yshk>/Ehmt2<tm1Yshk>	involves: C57BL/6 * CBA	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:107508	Ereg	Ereg<tm1Dwt>/Ereg<tm1Dwt>	129S6/SvEvTac-Ereg<tm1Dwt>	MP:0001263	weight loss	CCO:MP0001263
MGI:107508	Ereg	"Apc<Min>/Apc<+>,Ereg<tm1Dwt>/Ereg<tm1Dwt>"	involves: 129S6/SvEvTac * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:107508	Ereg	"Egf<tm1Dle>/Egf<tm1Dle>,Ereg<tm1Dwt>/Ereg<tm1Dwt>,Tgfa<tm1Unc>/Tgfa<tm1Unc>"	involves: 129S6/SvEvTac * C57BL/6J	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:107508	Ereg	"Egf<tm1Dle>/Egf<tm1Dle>,Ereg<tm1Dwt>/Ereg<tm1Dwt>,Tgfa<tm1Unc>/Tgfa<tm1Unc>"	involves: 129S6/SvEvTac * C57BL/6J	MP:0000410	waved hair	CCO:MP0000410
MGI:107508	Ereg	"Egfr<wa2>/Egfr<wa2>,Ereg<tm1Dwt>/Ereg<tm1Dwt>"	involves: 129S6/SvEvTac	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:107508	Ereg	Ereg<tm1Dwt>/Ereg<tm1Dwt>	129S6/SvEvTac-Ereg<tm1Dwt>	MP:0008873	increased sensitivity to xenobiotics	CCO:MP0008873
MGI:107508	Ereg	Ereg<tm1Sawa>/Ereg<tm1Sawa>	involves: 129X1/SvJ * C57BL/6J	MP:0001194	dermatitis	CCO:MP0001194
MGI:1930134	Ern1	Ern1<tm1Rjk>/Ern1<tm1Rjk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0005432	abnormal pro-B cell morphology	CCO:MP0005432
MGI:1930134	Ern1	Ern1<tm1Rjk>/Ern1<tm1Rjk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:1930134	Ern1	Ern1<tm1Rjk>/Ern1<tm1Rjk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1930134	Ern1	Ern1<tm1Rjk>/Ern1<tm1Rjk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1930134	Ern1	Ern1<tm1Rjk>/Ern1<tm1Rjk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003717	pallor	CCO:MP0003717
MGI:1930134	Ern1	Ern1<tm1Rjk>/Ern1<tm1Rjk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1930134	Ern1	Ern1<tm1Rjk>/Ern1<tm1Rjk>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1930134	Ern1	Ern1<tm1Rjk>/Ern1<tm1Rjk>	involves: 129S1/Sv * 129X1/SvJ	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1930134	Ern1	Ern1<tm1Dron>/Ern1<+>	129S.129S6-Ern1<tm1Dron>	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1930134	Ern1	Ern1<tm1Dron>/Ern1<+>	129S.129S6-Ern1<tm1Dron>	MP:0002078	abnormal glucose homeostasis	CCO:MP0002078
MGI:1930134	Ern1	Ern1<tm1Dron>/Ern1<tm1Dron>	involves: 129S6/SvEvTac	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1349436	Ern2	Ern2<tm1Dron>/Ern2<tm1Dron>	either: 129S6/SvEvTac-Ern2<tm1Dron> or B6.129S6-Ern2<tm1Dron>	MP:0008537	increased susceptibility to induced colitis	CCO:MP0008537
MGI:2146156	Espl1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:2146156	Espl1	Espl1<tm1.2Tno>/Espl1<tm1.2Tno>	involves: 129S4/SvJae * C57BL/6J	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:2146156	Espl1	Espl1<tm1.1Tno>/Espl1<+>	involves: 129S4/SvJae * C57BL/6J	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:2146156	Espl1	"Espl1<tm1.1Tno>/Espl1<+>,Pttg1<tm1Tno>/Pttg1<tm1Tno>"	involves: 129S4/SvJae * C57BL/6J	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:2146156	Espl1	"Espl1<tm1.2Tno>/Espl1<+>,Pttg1<tm1Tno>/Pttg1<tm1Tno>"	involves: 129S4/SvJae * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2146156	Espl1	"Espl1<tm1.2Tno>/Espl1<+>,Pttg1<tm1Tno>/Pttg1<tm1Tno>"	involves: 129S4/SvJae * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:2146156	Espl1	Espl1<tm1.1Tno>/Espl1<tm1.2Tno>	involves: 129S4/SvJae * C57BL/6J	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:2146156	Espl1	"Espl1<tm1.1Kna>/Espl1<tm1.1Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002658	abnormal liver regeneration	CCO:MP0002658
MGI:2146156	Espl1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:2146156	Espl1	"Espl1<tm1.1Kna>/Espl1<tm1.1Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:2146156	Espl1	Espl1<tm1.1Tno>/Espl1<tm1.2Tno>	involves: 129S4/SvJae * C57BL/6J	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:2146156	Espl1	"Espl1<tm1.1Kna>/Espl1<tm1.1Kna>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:2146156	Espl1	Espl1<tm1.2Tno>/Espl1<tm1.2Tno>	involves: 129S4/SvJae * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2146156	Espl1	Espl1<tm1.2Tno>/Espl1<tm1.2Tno>	involves: 129S4/SvJae * C57BL/6J	MP:0004957	abnormal blastocyst morphology	CCO:MP0004957
MGI:2146156	Espl1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2146156	Espl1	Espl1<tm1.2Tno>/Espl1<tm1.2Tno>	involves: 129S4/SvJae * C57BL/6J	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:2146156	Espl1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:2146156	Espl1	Espl1<tm1.2Kna>/Espl1<tm1.2Kna>	involves: 129P2/OlaHsd * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2146156	Espl1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:2146156	Espl1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:2146156	Espl1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:2146156	Espl1	"Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129S7/SvEvBrd	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:2146156	Espl1	"Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129S7/SvEvBrd	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:2146156	Espl1	"Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129S7/SvEvBrd	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:2146156	Espl1	"Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129S7/SvEvBrd	MP:0006378	abnormal spermatogonia morphology	CCO:MP0006378
MGI:2146156	Espl1	"Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129S7/SvEvBrd	MP:0006362	abnormal male germ cell morphology	CCO:MP0006362
MGI:2146156	Espl1	"Espl1<tm2Pzg>/Espl1<+>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129S7/SvEvBrd	MP:0001924	infertility	CCO:MP0001924
MGI:2146156	Espl1	Espl1<tm2Pzg>/Espl1<tm2Pzg>	involves: 129S7/SvEvBrd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0009140	dilated efferent ductules of testis	CCO:MP0009140
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0009359	endometrium atrophy	CCO:MP0009359
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0009097	absent endometrial glands	CCO:MP0009097
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0004896	abnormal endometrium morphology	CCO:MP0004896
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0003969	abnormal luteinizing hormone level	CCO:MP0003969
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0001123	dilated uterus	CCO:MP0001123
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0001926	female infertility	CCO:MP0001926
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0004933	abnormal epididymis epithelium morphology	CCO:MP0004933
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0009363	abnormal secondary ovarian follicle morphology	CCO:MP0009363
MGI:1352467	Esr1	"Esr1<tm1Gsc>/Esr1<tm1Gsc>,Tg(Camk2a-cre)2Gsc/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0009365	abnormal theca folliculi	CCO:MP0009365
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0002631	abnormal epididymis morphology	CCO:MP0002631
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0004850	abnormal testis weight	CCO:MP0004850
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0004728	abnormal efferent ductules of testis	CCO:MP0004728
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0003698	abnormal male reproductive system physiology	CCO:MP0003698
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0006423	dilated rete testis	CCO:MP0006423
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd	MP:0001925	male infertility	CCO:MP0001925
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<+>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	"Esr1<tm1Arnal>/Esr1<tm1Arnal>,Ldlr<tm1Her>/Ldlr<tm1Her>"	involves: 129S7/SvEvBrd	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	"Esr1<tm1Arnal>/Esr1<tm1Arnal>,Ldlr<tm1Her>/Ldlr<tm1Her>"	involves: 129S7/SvEvBrd	MP:0005339	increased susceptibility to atherosclerosis	CCO:MP0005339
MGI:1352467	Esr1	"Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cga-cre)3Sac/0"	involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	MP:0001927	abnormal estrous cycle	CCO:MP0001927
MGI:1352467	Esr1	"Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cga-cre)3Sac/0"	involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	MP:0002016	ovary cysts	CCO:MP0002016
MGI:1352467	Esr1	"Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cga-cre)3Sac/0"	involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Ldlr<tm1Her>/Ldlr<tm1Her>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Ldlr<tm1Her>/Ldlr<tm1Her>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0005339	increased susceptibility to atherosclerosis	CCO:MP0005339
MGI:1352467	Esr1	Esr1<tm1Arnal>/Esr1<tm1Arnal>	involves: C57BL/6	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	Esr1<tm1Arnal>/Esr1<tm1Arnal>	involves: C57BL/6	MP:0001924	infertility	CCO:MP0001924
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0009363	abnormal secondary ovarian follicle morphology	CCO:MP0009363
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0006416	abnormal rete testis morphology	CCO:MP0006416
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0003357	impaired granulosa cell differentiation	CCO:MP0003357
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0009081	thin uterus	CCO:MP0009081
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0006416	abnormal rete testis morphology	CCO:MP0006416
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0008984	vagina hypoplasia	CCO:MP0008984
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0009082	uterus cysts	CCO:MP0009082
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0008869	anovulation	CCO:MP0008869
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0003357	impaired granulosa cell differentiation	CCO:MP0003357
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0008983	small vagina	CCO:MP0008983
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0001139	abnormal vagina morphology	CCO:MP0001139
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0005182	increased circulating estradiol level	CCO:MP0005182
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0002781	increased circulating testosterone level	CCO:MP0002781
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0002637	small uterus	CCO:MP0002637
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0001751	increased circulating luteinizing hormone level	CCO:MP0001751
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0001121	uterus hypoplasia	CCO:MP0001121
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0002016	ovary cysts	CCO:MP0002016
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<+>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0001120	abnormal uterus morphology	CCO:MP0001120
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0001260	increased body weight	CCO:MP0001260
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0001264	increased body size	CCO:MP0001264
MGI:1352467	Esr1	Esr1<tm2Ksk>/Esr1<tm2Ksk>	involves: C57BL/6	MP:0001751	increased circulating luteinizing hormone level	CCO:MP0001751
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0009363	abnormal secondary ovarian follicle morphology	CCO:MP0009363
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0004904	increased uterus weight	CCO:MP0004904
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0003355	decreased ovulation frequency	CCO:MP0003355
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0005185	decreased circulating progesterone level	CCO:MP0005185
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0001926	female infertility	CCO:MP0001926
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0003357	impaired granulosa cell differentiation	CCO:MP0003357
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0009371	increased thecal cell number	CCO:MP0009371
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0009296	increased mammary fat pad weight	CCO:MP0009296
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0009285	increased gonadal fat pad weight	CCO:MP0009285
MGI:1352467	Esr1	Esr1<tm1Geog>/Esr1<tm1Geog>	involves: 129X1/SvJ * C57BL/6	MP:0008984	vagina hypoplasia	CCO:MP0008984
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0002784	abnormal Sertoli cell morphology	CCO:MP0002784
MGI:1352467	Esr1	"Esr1<tm1.2Mma>/Esr1<tm1.2Mma>,Tg(Cga-cre)3Sac/0"	involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL	MP:0001926	female infertility	CCO:MP0001926
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0004906	enlarged uterus	CCO:MP0004906
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0009092	endometrium hyperplasia	CCO:MP0009092
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0009363	abnormal secondary ovarian follicle morphology	CCO:MP0009363
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0003109	short femur	CCO:MP0003109
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0000062	increased bone density	CCO:MP0000062
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001926	female infertility	CCO:MP0001926
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6	MP:0004905	decreased uterus weight	CCO:MP0004905
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6	MP:0000063	decreased bone density	CCO:MP0000063
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6	MP:0000062	increased bone density	CCO:MP0000062
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0004904	increased uterus weight	CCO:MP0004904
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0004016	decreased bone mass	CCO:MP0004016
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0003795	abnormal bone structure	CCO:MP0003795
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0000063	decreased bone density	CCO:MP0000063
MGI:1352467	Esr1	"Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0000063	decreased bone density	CCO:MP0000063
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0002016	ovary cysts	CCO:MP0002016
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001925	male infertility	CCO:MP0001925
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1352467	Esr1	"Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0000066	osteoporosis	CCO:MP0000066
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0005182	increased circulating estradiol level	CCO:MP0005182
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0004905	decreased uterus weight	CCO:MP0004905
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0004701	decreased circulating insulin-like growth factor I level	CCO:MP0004701
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0004016	decreased bone mass	CCO:MP0004016
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0003795	abnormal bone structure	CCO:MP0003795
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0003109	short femur	CCO:MP0003109
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0009251	enlarged endometrial glands	CCO:MP0009251
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1352467	Esr1	"Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0004992	increased bone resorption	CCO:MP0004992
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0009009	absent estrous cycle	CCO:MP0009009
MGI:1352467	Esr1	"Esr1<tm1.1Mma>/Esr1<tm1.1Mma>,Esr2<tm1Mma>/Esr2<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001121	uterus hypoplasia	CCO:MP0001121
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0008984	vagina hypoplasia	CCO:MP0008984
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0003638	abnormal response/metabolism to endogenous compounds	CCO:MP0003638
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0002016	ovary cysts	CCO:MP0002016
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0000063	decreased bone density	CCO:MP0000063
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<+>	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0009671	abnormal uterus physiology	CCO:MP0009671
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001121	uterus hypoplasia	CCO:MP0001121
MGI:1352467	Esr1	"Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0004984	increased osteoclast cell number	CCO:MP0004984
MGI:1352467	Esr1	"Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:1352467	Esr1	"Ctsk<tm1(cre)Ska>/Ctsk<+>,Esr1<tm1Mma>/Esr1<tm1Mma>"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001541	abnormal osteoclast physiology	CCO:MP0001541
MGI:1352467	Esr1	Esr1<tm1.1Mma>/Esr1<tm1.1Mma>	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:1352467	Esr1	Esr1<tm1.1Lja>/Esr1<tm1.1Mma>	involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0001541	abnormal osteoclast physiology	CCO:MP0001541
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0002781	increased circulating testosterone level	CCO:MP0002781
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	B6.129P2-Esr1<tm1Ksk>/J	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	B6.129P2-Esr1<tm1Ksk>/J	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0009362	abnormal primary ovarian follicle morphology	CCO:MP0009362
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0009361	abnormal primordial ovarian follicle morphology	CCO:MP0009361
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0008984	vagina hypoplasia	CCO:MP0008984
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0008868	abnormal granulosa cell morphology	CCO:MP0008868
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0008256	abnormal myometrium morphology	CCO:MP0008256
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0005453	increased adipose tissue amount	CCO:MP0005453
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001121	uterus hypoplasia	CCO:MP0001121
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001129	impaired ovarian folliculogenesis	CCO:MP0001129
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0003607	abnormal prostate physiology	CCO:MP0003607
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001925	male infertility	CCO:MP0001925
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001919	abnormal reproductive system physiology	CCO:MP0001919
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001261	obese	CCO:MP0001261
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001147	small testis	CCO:MP0001147
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0002016	ovary cysts	CCO:MP0002016
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001926	female infertility	CCO:MP0001926
MGI:1352467	Esr1	"Esr1<tm1Syeh>/Esr1<tm1Syeh>,Tg(ACTB-cre)2Mrt/0"	involves: 129X1/SvJ * FVB/N	MP:0001158	abnormal prostate morphology	CCO:MP0001158
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001926	female infertility	CCO:MP0001926
MGI:1352467	Esr1	"Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>"	involves: 129P2/OlaHsd	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002016	ovary cysts	CCO:MP0002016
MGI:1352467	Esr1	"Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>"	involves: 129P2/OlaHsd	MP:0001925	male infertility	CCO:MP0001925
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002781	increased circulating testosterone level	CCO:MP0002781
MGI:1352467	Esr1	"Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>"	involves: 129P2/OlaHsd	MP:0001121	uterus hypoplasia	CCO:MP0001121
MGI:1352467	Esr1	"Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>"	involves: 129P2/OlaHsd	MP:0001751	increased circulating luteinizing hormone level	CCO:MP0001751
MGI:1352467	Esr1	"Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>"	involves: 129P2/OlaHsd	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0009257	dilated seminiferous tubules	CCO:MP0009257
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1352467	Esr1	"Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>"	involves: 129P2/OlaHsd	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002631	abnormal epididymis morphology	CCO:MP0002631
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001121	uterus hypoplasia	CCO:MP0001121
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005656	decreased aggression	CCO:MP0005656
MGI:1352467	Esr1	"Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>"	involves: 129P2/OlaHsd	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001380	male reduced copulation	CCO:MP0001380
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006304	abnormal seminiferous epithelium morphology	CCO:MP0006304
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0008893	detached sperm flagellum	CCO:MP0008893
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0006423	dilated rete testis	CCO:MP0006423
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001399	hyperactivity	CCO:MP0001399
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002574	increased vertical activity	CCO:MP0002574
MGI:1352467	Esr1	"Esr1<tm1Ksk>/Esr1<tm1Ksk>,Esr2<tm1Unc>/Esr2<tm1Unc>"	involves: 129P2/OlaHsd	MP:0001926	female infertility	CCO:MP0001926
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001376	abnormal mating receptivity	CCO:MP0001376
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005578	teratozoospermia	CCO:MP0005578
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001356	increased aggression towards females	CCO:MP0001356
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001384	abnormal pup retrieval	CCO:MP0001384
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001386	abnormal maternal nurturing	CCO:MP0001386
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001385	pup cannibalization	CCO:MP0001385
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000242	impaired fertilization	CCO:MP0000242
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001147	small testis	CCO:MP0001147
MGI:1352467	Esr1	Esr1<tm1Ksk>/Esr1<tm1Ksk>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001378	abnormal ejaculation	CCO:MP0001378
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0001147	small testis	CCO:MP0001147
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0001127	small ovary	CCO:MP0001127
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0009564	abnormal meiotic configurations	CCO:MP0009564
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0008966	abnormal chiasmata formation	CCO:MP0008966
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0001925	male infertility	CCO:MP0001925
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0001926	female infertility	CCO:MP0001926
MGI:1349427	Exo1	Exo1<tm1Wed>/Exo1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0008967	absent chiasmata formation	CCO:MP0008967
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0004030	induced chromosome breakage	CCO:MP0004030
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<+>	involves: 129P2/OlaHsd * FVB	MP:0004030	induced chromosome breakage	CCO:MP0004030
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0002590	increased mean corpuscular volume	CCO:MP0002590
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0001935	decreased litter size	CCO:MP0001935
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0001152	Leydig cell hyperplasia	CCO:MP0001152
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0001116	small gonad	CCO:MP0001116
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:1341823	Fanca	Fanca<tm1Faw>/Fanca<tm1Faw>	involves: 129P2/OlaHsd * FVB/N	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:1341823	Fanca	Fanca<tm1Zqw>/Fanca<tm1Zqw>	involves: 129P2/OlaHsd	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0000438	abnormal skull morphology	CCO:MP0000438
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0002209	decreased germ cell number	CCO:MP0002209
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * CD-1)	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:1341823	Fanca	Fanca<tm1.1Wong>/Fanca<tm1.1Wong>	involves: C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	MP:0005158	ovary hypoplasia	CCO:MP0005158
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	MP:0008995	early reproductive senescence	CCO:MP0008995
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: C57BL/6	MP:0000438	abnormal skull morphology	CCO:MP0000438
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: C57BL/6	MP:0002209	decreased germ cell number	CCO:MP0002209
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	MP:0004834	ovary hemorrhage	CCO:MP0004834
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	MP:0001147	small testis	CCO:MP0001147
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	MP:0002209	decreased germ cell number	CCO:MP0002209
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	involves: 129S6/SvEvTac	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	MP:0001127	small ovary	CCO:MP0001127
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	MP:0002682	decreased mature ovarian follicle number	CCO:MP0002682
MGI:1341823	Fanca	Fanca<tm1Wong>/Fanca<tm1Wong>	either: 129S6/SvEvTac or C57BL/6	MP:0002016	ovary cysts	CCO:MP0002016
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:2448480	Fancd2	"Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>,Usp1<tm1.1Ada>/Usp1<tm1.1Ada>"	involves: 129S/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:2448480	Fancd2	"Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>,Usp1<tm1.1Ada>/Usp1<tm1.1Ada>"	involves: 129S/SvEvBrd * C57BL/6	MP:0004833	ovary atrophy	CCO:MP0004833
MGI:2448480	Fancd2	"Dclre1a<tm1Remo>/Dclre1a<tm1Remo>,Fancd2<tm1Hou>/Fancd2<tm1Hou>"	involves: 129S4/SvJae * 129X1/SvJ * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0002815	adenoma	CCO:MP0002815
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0002682	decreased mature ovarian follicle number	CCO:MP0002682
MGI:2448480	Fancd2	"Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>,Usp1<tm1.1Ada>/Usp1<tm1.1Ada>"	involves: 129S/SvEvBrd * C57BL/6	MP:0004030	induced chromosome breakage	CCO:MP0004030
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	involves: 129S4/SvJae	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0004201	fetal growth retardation	CCO:MP0004201
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:2448480	Fancd2	Fancd2<Gt(OST57859)Lex>/Fancd2<Gt(OST57859)Lex>	involves: 129S/SvEvBrd * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	B6.129S4-Fancd2<tm1Hou>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	B6.129S4-Fancd2<tm1Hou>	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	B6.129S4-Fancd2<tm1Hou>	MP:0001297	microphthalmia	CCO:MP0001297
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	B6.129S4-Fancd2<tm1Hou>	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	B6.129S4-Fancd2<tm1Hou>	MP:0004201	fetal growth retardation	CCO:MP0004201
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	MP:0002038	carcinoma	CCO:MP0002038
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	MP:0002682	decreased mature ovarian follicle number	CCO:MP0002682
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	involves: 129S4/SvJae * C57BL/6J	MP:0002815	adenoma	CCO:MP0002815
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	MP:0001147	small testis	CCO:MP0001147
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	involves: 129S4/SvJae * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:2448480	Fancd2	Fancd2<tm1Hou>/Fancd2<tm1Hou>	129S4/SvJae-Fancd2<tm1Hou>	MP:0002815	adenoma	CCO:MP0002815
MGI:1914391	Fbxo5	Fbxo5<tm1Dlim>/Fbxo5<tm1Dlim>	involves: 129S4/SvJaeSor	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1914391	Fbxo5	Fbxo5<tm1Dlim>/Fbxo5<tm1Dlim>	involves: 129S4/SvJaeSor	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1914391	Fbxo5	Fbxo5<tm1Dlim>/Fbxo5<tm1Dlim>	involves: 129S4/SvJaeSor	MP:0005031	abnormal trophoblast layer morphology	CCO:MP0005031
MGI:1914391	Fbxo5	Fbxo5<tm1Dlim>/Fbxo5<tm1Dlim>	involves: 129S4/SvJaeSor	MP:0002663	failure to form blastocele	CCO:MP0002663
MGI:1914391	Fbxo5	Fbxo5<tm1Dlim>/Fbxo5<tm1Dlim>	involves: 129S4/SvJaeSor	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1914391	Fbxo5	Fbxo5<tm1Dlim>/Fbxo5<tm1Dlim>	involves: 129S4/SvJaeSor	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0005312	pericardial effusion	CCO:MP0005312
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0003105	abnormal heart atrium morphology	CCO:MP0003105
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0008022	dilated heart ventricles	CCO:MP0008022
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<tm1.1Mrt>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0004158	right aortic arch	CCO:MP0004158
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0002127	abnormal cardiovascular system morphology	CCO:MP0002127
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<tm1.1Mrt>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0004157	interrupted aortic arch	CCO:MP0004157
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0003920	abnormal heart right ventricle morphology	CCO:MP0003920
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<tm1.1Mrt>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0004160	retroesophageal right subclavian artery	CCO:MP0004160
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0004110	transposition of great arteries	CCO:MP0004110
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<tm1.1Mrt>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0002950	abnormal neural crest cell migration	CCO:MP0002950
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0004201	fetal growth retardation	CCO:MP0004201
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Fgf17<tm1Dor>/Fgf17<tm1Dor>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0000867	abnormal anterior vermis	CCO:MP0000867
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Fgf17<tm1Dor>/Fgf17<tm1Dor>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0000864	abnormal vermis morphology	CCO:MP0000864
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0001785	edema	CCO:MP0001785
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Fgf17<tm1Dor>/Fgf17<tm1Dor>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Fgf17<tm1Dor>/Fgf17<tm1Dor>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0001406	abnormal gait	CCO:MP0001406
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0002748	abnormal pulmonary valve morphology	CCO:MP0002748
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0006356	abnormal third branchial arch artery morphology	CCO:MP0006356
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0002747	abnormal aortic valve morphology	CCO:MP0002747
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0002949	abnormal neural crest cells	CCO:MP0002949
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0001575	cyanosis	CCO:MP0001575
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Isl1<tm1(cre)Sev>/Isl1<+>"	Not Specified	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Mesp1<tm2(cre)Ysa>/Mesp1<+>"	involves: C57BL/6 * CBA	MP:0000270	abnormal heart tube morphology	CCO:MP0000270
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<+>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0004160	retroesophageal right subclavian artery	CCO:MP0004160
MGI:99604	Fgf8	"Fgf8<tm1.1Mrt>/Fgf8<tm1.4Mrt>,Foxg1<tm1M>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003202	abnormal neuron apoptosis	CCO:MP0003202
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<+>,Tbx1<tm4(cre/Esr1)Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tbx1<tm4(cre/Esr1)Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Fgf17<tm1Dor>/Fgf17<tm1Dor>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0009038	decreased inferior colliculus size	CCO:MP0009038
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0006331	abnormal patterning of the organ of Corti	CCO:MP0006331
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0004312	absent pillar cells	CCO:MP0004312
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003825	abnormal pillar cell morphology	CCO:MP0003825
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003308	abnormal cochlear sensory epithelium morphology	CCO:MP0003308
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003232	abnormal forebrain development	CCO:MP0003232
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003152	abnormal pillar cell differentiation	CCO:MP0003152
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Isl1<tm1(cre)Sev>/Isl1<+>"	Not Specified	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<+>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0002127	abnormal cardiovascular system morphology	CCO:MP0002127
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Tg(Mef2c-cre)2Blk/0"	Not Specified	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Tbx1<tm4(cre/Esr1)Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Isl1<tm1(cre)Sev>/Isl1<+>"	Not Specified	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:99604	Fgf8	"Fgf8<tm1.1Mrt>/Fgf8<tm1.4Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Isl1<tm1(cre)Sev>/Isl1<+>"	Not Specified	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Isl1<tm1(cre)Sev>/Isl1<+>"	Not Specified	MP:0003920	abnormal heart right ventricle morphology	CCO:MP0003920
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Isl1<tm1(cre)Sev>/Isl1<+>"	Not Specified	MP:0006346	small branchial arch	CCO:MP0006346
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<tm1.1Mrt>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0000704	abnormal thymus development	CCO:MP0000704
MGI:99604	Fgf8	"Fgf8<tm2Moon>/Fgf8<tm1Mrc>,Tg(Mef2c-cre)2Blk/0"	Not Specified	MP:0004110	transposition of great arteries	CCO:MP0004110
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<tm1.1Mrt>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0000018	small ears	CCO:MP0000018
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<tm1.1Mrt>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0000088	short mandible	CCO:MP0000088
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm3Mrc>	involves: 129/Sv * C57BL/6	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<tm1.1Mrt>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0002127	abnormal cardiovascular system morphology	CCO:MP0002127
MGI:99604	Fgf8	"Gbx2<tm1.1Mrt>/Gbx2<+>,Fgf8<tm1.4Mrt>/Fgf8<+>"	B6.129-Gbx2<tm1.1Mrt> Fgf8<tm1.4Mrt>	MP:0004158	right aortic arch	CCO:MP0004158
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Gli3<tm1.1Alj>/Gli3<tm1.1Alj>"	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	MP:0009048	enlarged tectum	CCO:MP0009048
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Gli3<tm1.1Alj>/Gli3<tm1.1Alj>"	involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6	MP:0009039	absent inferior colliculus	CCO:MP0009039
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002753	dilated heart left ventricle	CCO:MP0002753
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0000270	abnormal heart tube morphology	CCO:MP0000270
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm2Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129 * 129S7/SvEvBrd	MP:0004759	decreased mitotic index	CCO:MP0004759
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0003140	dilated atria	CCO:MP0003140
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<+>,Fgf9<tm1Dor>/Fgf9<+>,Fgfr3<tm1.1Aomw>/Fgfr3<+>"	involves: 129 * BALB/c * C57BL/6	MP:0004765	decreased brainstem auditory evoked potential	CCO:MP0004765
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Moon>,Isl1<tm1(cre)Sev>/Isl1<+>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0000297	abnormal endocardial cushion morphology	CCO:MP0000297
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Moon>,Isl1<tm1(cre)Sev>/Isl1<+>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm2Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129 * 129S7/SvEvBrd	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?"	involves: 129P2/OlaHsd	MP:0008919	fused tarsal bones	CCO:MP0008919
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?"	involves: 129P2/OlaHsd	MP:0001340	abnormal eyelid morphology	CCO:MP0001340
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?"	involves: 129P2/OlaHsd	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?"	involves: 129P2/OlaHsd	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?"	involves: 129P2/OlaHsd	MP:0005650	abnormal limb bud morphology	CCO:MP0005650
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?"	involves: 129P2/OlaHsd	MP:0004083	polysyndactyly	CCO:MP0004083
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<+>,Fgfr3<tm1.1Aomw>/Fgfr3<+>"	involves: 129 * BALB/c * C57BL/6	MP:0006325	impaired hearing	CCO:MP0006325
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<+>,Fgf9<tm1Dor>/Fgf9<+>,Fgfr3<tm1.1Aomw>/Fgfr3<+>"	involves: 129 * BALB/c * C57BL/6	MP:0006325	impaired hearing	CCO:MP0006325
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Gt(ROSA)26Sor<tm1Sor>/Gt(ROSA)26Sor<tm1Sor>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S7/SvEvBrd	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm2Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129 * 129S7/SvEvBrd	MP:0002884	abnormal branchial arch morphology	CCO:MP0002884
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Moon>,Isl1<tm1(cre)Sev>/Isl1<+>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm2Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129 * 129S7/SvEvBrd	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm2Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129 * 129S7/SvEvBrd	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0003873	branchial arch hypoplasia	CCO:MP0003873
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Nkx2-5<tm1(cre)Rjs>/Nkx2-5<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0003872	absent heart right ventricle	CCO:MP0003872
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?"	involves: 129P2/OlaHsd	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(CAG-Bgeo,-Fgf4)1Mrt/?,Tg(Msx2-cre)5Rem/?"	involves: 129P2/OlaHsd	MP:0006279	abnormal limb development	CCO:MP0006279
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<+>,Fgfr3<tm1.1Aomw>/Fgfr3<+>"	involves: 129 * BALB/c * C57BL/6	MP:0004765	decreased brainstem auditory evoked potential	CCO:MP0004765
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tg(Rarb-cre)1Mrc/0"	Not Specified	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tg(Rarb-cre)1Mrc/0"	Not Specified	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tg(Rarb-cre)1Mrc/0"	Not Specified	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0001726	abnormal allantois morphology	CCO:MP0001726
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0002231	abnormal primitive streak morphology	CCO:MP0002231
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0005029	abnormal amnion morphology	CCO:MP0005029
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0003886	abnormal embryonic epiblast morphology	CCO:MP0003886
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0009331	absent primitive node	CCO:MP0009331
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0001675	abnormal ectoderm development	CCO:MP0001675
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0001726	abnormal allantois morphology	CCO:MP0001726
MGI:99604	Fgf8	Fgf8<tm2Mrc>/Fgf8<tm2Mrc>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0002836	abnormal chorion morphology	CCO:MP0002836
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0000850	absent cerebellum	CCO:MP0000850
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.1Mrt>	involves: 129P2/OlaHsd	MP:0003451	absent olfactory bulb	CCO:MP0003451
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0000564	syndactyly	CCO:MP0000564
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0001680	abnormal mesoderm development	CCO:MP0001680
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0000897	abnormal midbrain morphology	CCO:MP0000897
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0005029	abnormal amnion morphology	CCO:MP0005029
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0005221	abnormal rostral-caudal axis patterning	CCO:MP0005221
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0003935	abnormal craniofacial development	CCO:MP0003935
MGI:99604	Fgf8	Fgf8<tm1.3Mrt>/Fgf8<tm1.3Mrt>	involves: 129P2/OlaHsd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>	involves: 129P2/OlaHsd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0003857	abnormal hindlimb zeugopod morphology	CCO:MP0003857
MGI:99604	Fgf8	Fgf8<tm1.4Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0001675	abnormal ectoderm development	CCO:MP0001675
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0000936	small telencephalic vesicles	CCO:MP0000936
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0001065	abnormal trigeminal nerve morphology	CCO:MP0001065
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0000455	abnormal maxilla morphology	CCO:MP0000455
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0000458	abnormal mandible morphology	CCO:MP0000458
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0009331	absent primitive node	CCO:MP0009331
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0003886	abnormal embryonic epiblast morphology	CCO:MP0003886
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0006255	small tongue	CCO:MP0006255
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0003931	absent molars	CCO:MP0003931
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0003935	abnormal craniofacial development	CCO:MP0003935
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0006279	abnormal limb development	CCO:MP0006279
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0004439	absent Meckel's cartilage	CCO:MP0004439
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm2Mrc>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0002836	abnormal chorion morphology	CCO:MP0002836
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.1Mrt>	involves: 129P2/OlaHsd	MP:0000850	absent cerebellum	CCO:MP0000850
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0001680	abnormal mesoderm development	CCO:MP0001680
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0000565	oligodactyly	CCO:MP0000565
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0000553	absent radius	CCO:MP0000553
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0003854	abnormal forelimb stylopod morphology	CCO:MP0003854
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0003855	abnormal forelimb zeugopod morphology	CCO:MP0003855
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0003856	abnormal hindlimb stylopod morphology	CCO:MP0003856
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0006341	small first branchial arch	CCO:MP0006341
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Msx2-cre)5Rem/0"	involves: 129P2/OlaHsd	MP:0004575	small limb buds	CCO:MP0004575
MGI:99604	Fgf8	Fgf8<tm1Mrc>/Fgf8<tm1Mrc>	Not Specified	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:99604	Fgf8	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Tg(Nes-cre)1Mrt/0"	involves: 129P2/OlaHsd	MP:0004318	absent incus	CCO:MP0004318
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0004158	right aortic arch	CCO:MP0004158
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0001675	abnormal ectoderm development	CCO:MP0001675
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0004158	right aortic arch	CCO:MP0004158
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0002747	abnormal aortic valve morphology	CCO:MP0002747
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0004157	interrupted aortic arch	CCO:MP0004157
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0004160	retroesophageal right subclavian artery	CCO:MP0004160
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0004111	abnormal coronary artery morphology	CCO:MP0004111
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0003873	branchial arch hypoplasia	CCO:MP0003873
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0006355	abnormal sixth branchial arch artery morphology	CCO:MP0006355
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0006354	abnormal fourth branchial arch artery morphology	CCO:MP0006354
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0006356	abnormal third branchial arch artery morphology	CCO:MP0006356
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0002949	abnormal neural crest cells	CCO:MP0002949
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0003007	ectopic thymus	CCO:MP0003007
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0000678	abnormal parathyroid gland morphology	CCO:MP0000678
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0004111	abnormal coronary artery morphology	CCO:MP0004111
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0002672	abnormal branchial arch artery morphology	CCO:MP0002672
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0006356	abnormal third branchial arch artery morphology	CCO:MP0006356
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0000678	abnormal parathyroid gland morphology	CCO:MP0000678
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.1Mrt>	involves: 129P2/OlaHsd	MP:0000897	abnormal midbrain morphology	CCO:MP0000897
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0003395	abnormal subclavian artery morphology	CCO:MP0003395
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0004160	retroesophageal right subclavian artery	CCO:MP0004160
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0006355	abnormal sixth branchial arch artery morphology	CCO:MP0006355
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0006356	abnormal third branchial arch artery morphology	CCO:MP0006356
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0002672	abnormal branchial arch artery morphology	CCO:MP0002672
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0006354	abnormal fourth branchial arch artery morphology	CCO:MP0006354
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0004157	interrupted aortic arch	CCO:MP0004157
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0006354	abnormal fourth branchial arch artery morphology	CCO:MP0006354
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0004111	abnormal coronary artery morphology	CCO:MP0004111
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0003873	branchial arch hypoplasia	CCO:MP0003873
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0003395	abnormal subclavian artery morphology	CCO:MP0003395
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0002949	abnormal neural crest cells	CCO:MP0002949
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0002672	abnormal branchial arch artery morphology	CCO:MP0002672
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Tcfap2a<tm1(cre)Moon>/Tcfap2a<+>"	involves: 129/Sv * C57BL/6	MP:0002949	abnormal neural crest cells	CCO:MP0002949
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0006354	abnormal fourth branchial arch artery morphology	CCO:MP0006354
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm2Mrc>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0003494	parathyroid hypoplasia	CCO:MP0003494
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0001680	abnormal mesoderm development	CCO:MP0001680
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0009331	absent primitive node	CCO:MP0009331
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0003886	abnormal embryonic epiblast morphology	CCO:MP0003886
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0002949	abnormal neural crest cells	CCO:MP0002949
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0003007	ectopic thymus	CCO:MP0003007
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0004111	abnormal coronary artery morphology	CCO:MP0004111
MGI:99604	Fgf8	Fgf8<tm1.1Mrt>/Fgf8<tm1.1Mrt>	involves: 129P2/OlaHsd	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0006356	abnormal third branchial arch artery morphology	CCO:MP0006356
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0002231	abnormal primitive streak morphology	CCO:MP0002231
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0001726	abnormal allantois morphology	CCO:MP0001726
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0002836	abnormal chorion morphology	CCO:MP0002836
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0005029	abnormal amnion morphology	CCO:MP0005029
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0003494	parathyroid hypoplasia	CCO:MP0003494
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.2Mrt>	involves: 129P2/OlaHsd	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:99604	Fgf8	Fgf8<tm1.2Mrt>/Fgf8<tm1.4Mrt>	involves: 129P2/OlaHsd	MP:0002231	abnormal primitive streak morphology	CCO:MP0002231
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0002672	abnormal branchial arch artery morphology	CCO:MP0002672
MGI:99604	Fgf8	"Fgf8<tm1Mrc>/Fgf8<tm1Moon>,Hoxa3<tm1(cre)Moon>/Hoxa3<+>"	involves: 129/Sv * C57BL/6	MP:0002747	abnormal aortic valve morphology	CCO:MP0002747
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Tbx1<tm1Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Tbx1<tm1Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR	MP:0004158	right aortic arch	CCO:MP0004158
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0000706	small thymus	CCO:MP0000706
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0005592	abnormal vascular smooth muscle morphology	CCO:MP0005592
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0004110	transposition of great arteries	CCO:MP0004110
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0004181	abnormal carotid artery morphology	CCO:MP0004181
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(T-cre)1Lwd/0"	involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1	MP:0004936	abnormal ureteric bud branching morphogenesis	CCO:MP0004936
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Tbx1<tm1Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR	MP:0006354	abnormal fourth branchial arch artery morphology	CCO:MP0006354
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(T-cre)1Lwd/0"	involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(T-cre)1Lwd/0"	involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1	MP:0000527	abnormal kidney development	CCO:MP0000527
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(T-cre)1Lwd/0"	involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1	MP:0006032	abnormal ureteric bud morphology	CCO:MP0006032
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(T-cre)1Lwd/0"	involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1	MP:0003606	kidney failure	CCO:MP0003606
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0004044	aortic dissection	CCO:MP0004044
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Tbx1<tm1Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Tbx1<tm1Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR	MP:0004161	cervical aortic arch	CCO:MP0004161
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Tbx1<tm1Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR	MP:0004157	interrupted aortic arch	CCO:MP0004157
MGI:99604	Fgf8	"Fgf8<tm1.4Mrt>/Fgf8<+>,Tbx1<tm1Bld>/Tbx1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * ICR	MP:0002977	abnormal patterning of the aortic arch	CCO:MP0002977
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0002127	abnormal cardiovascular system morphology	CCO:MP0002127
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(T-cre)1Lwd/0"	involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1	MP:0000565	oligodactyly	CCO:MP0000565
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0000703	abnormal thymus morphology	CCO:MP0000703
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(T-cre)1Lwd/0"	involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:99604	Fgf8	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Tg(Tbx1-cre)1Joe/0"	Not Specified	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1859252	Fmn2	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0001382	abnormal nursing	CCO:MP0001382
MGI:1859252	Fmn2	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1859252	Fmn2	Fmn2<tm1Led>/Fmn2<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1347464	Foxg1	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0000936	small telencephalic vesicles	CCO:MP0000936
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0004399	abnormal cochlear outer hair cell morphology	CCO:MP0004399
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0000031	abnormal cochlea morphology	CCO:MP0000031
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0000042	abnormal organ of Corti	CCO:MP0000042
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0003308	abnormal cochlear sensory epithelium morphology	CCO:MP0003308
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0004301	absent supporting cells	CCO:MP0004301
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0004403	absent cochlear outer hair cells	CCO:MP0004403
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0004408	decreased cochlear hair cell number	CCO:MP0004408
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0004492	abnormal orientation of inner hair cell stereociliary bundles	CCO:MP0004492
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0004589	abnormal cochlear hair cell development	CCO:MP0004589
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0000042	abnormal organ of Corti	CCO:MP0000042
MGI:1347464	Foxg1	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0004405	absent cochlear hair cells	CCO:MP0004405
MGI:1347464	Foxg1	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0000031	abnormal cochlea morphology	CCO:MP0000031
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0000037	abnormal lateral semicircular canal	CCO:MP0000037
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0000036	absent semicircular canals	CCO:MP0000036
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0002622	abnormal cochlear hair cell morphology	CCO:MP0002622
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0004336	small utricle	CCO:MP0004336
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0004333	abnormal utricular macula morphology	CCO:MP0004333
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0004249	abnormal crista ampullaris morphology	CCO:MP0004249
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0006089	abnormal saccule morphology	CCO:MP0006089
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0003151	absent tunnel of Corti	CCO:MP0003151
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0003148	decreased cochlear coiling	CCO:MP0003148
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0003069	abnormal superior semicircular canal	CCO:MP0003069
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0003308	abnormal cochlear sensory epithelium morphology	CCO:MP0003308
MGI:1347464	Foxg1	"Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>,Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:1347464	Foxg1	"Dll1<tm1Mjo>/Dll1<tm1Mjo>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0004330	abnormal saccular macula morphology	CCO:MP0004330
MGI:1347464	Foxg1	"Dll1<tm1Mjo>/Dll1<tm1Mjo>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0003148	decreased cochlear coiling	CCO:MP0003148
MGI:1347464	Foxg1	"Dll1<tm1Mjo>/Dll1<tm1Mjo>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0002622	abnormal cochlear hair cell morphology	CCO:MP0002622
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd	MP:0005319	abnormal enzyme/ coenzyme level	CCO:MP0005319
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd	MP:0006035	abnormal mitochondrial morphology	CCO:MP0006035
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd	MP:0006036	abnormal mitochondrial physiology	CCO:MP0006036
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd	MP:0006039	decreased mitochondrial proliferation	CCO:MP0006039
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd	MP:0006254	thin cerebral cortex	CCO:MP0006254
MGI:1347464	Foxg1	"Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>,Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0000789	thickened cerebral cortex	CCO:MP0000789
MGI:1347464	Foxg1	"Fgfr1<tm1Upir>/Fgfr1<tm1.1Upir>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * ICR	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1347464	Foxg1	"Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>,Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:1347464	Foxg1	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Jlew>/Jag1<tm1Jlew>"	involves: C57BL/6J	MP:0002428	abnormal semicircular canal	CCO:MP0002428
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Jlew>/Jag1<tm1Jlew>"	involves: C57BL/6J	MP:0002622	abnormal cochlear hair cell morphology	CCO:MP0002622
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Jlew>/Jag1<tm1Jlew>"	involves: C57BL/6J	MP:0004325	absent vestibular hair cells	CCO:MP0004325
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Jlew>/Jag1<tm1Jlew>"	involves: C57BL/6J	MP:0004333	abnormal utricular macula morphology	CCO:MP0004333
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Jlew>/Jag1<tm1Jlew>"	involves: C57BL/6J	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Jlew>/Jag1<tm1Jlew>"	involves: C57BL/6J	MP:0004403	absent cochlear outer hair cells	CCO:MP0004403
MGI:1347464	Foxg1	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0004261	abnormal embryonic neuroepithelium morphology	CCO:MP0004261
MGI:1347464	Foxg1	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0005157	holoprosencephaly	CCO:MP0005157
MGI:1347464	Foxg1	"Cdc42<tm1Yizh>/Cdc42<tm1Yizh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0000935	abnormal folding of telencephalic vesicles	CCO:MP0000935
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Jag1<tm1Grid>/Jag1<tm2Grid>"	involves: 129P2/OlaHsd * 129S1/Sv	MP:0004406	abnormal cochlear hair cell number	CCO:MP0004406
MGI:1347464	Foxg1	"Dll1<tm1Mjo>/Dll1<tm1Mjo>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0004401	increased cochlear outer hair cell number	CCO:MP0004401
MGI:1347464	Foxg1	"Dll1<tm1Mjo>/Dll1<tm1Mjo>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0004333	abnormal utricular macula morphology	CCO:MP0004333
MGI:1347464	Foxg1	"Apaf1<Gt(IRESBetageo)XIX18Pgr>/Apaf1<Gt(IRESBetageo)XIX18Pgr>,Foxg1<tm1(cre)Skm>/Foxg1<+>,Aifm1<tm2Pngr>/Y"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ	MP:0006036	abnormal mitochondrial physiology	CCO:MP0006036
MGI:1347464	Foxg1	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003232	abnormal forebrain development	CCO:MP0003232
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004236	absent masseter muscle	CCO:MP0004236
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004238	absent pterygoid muscle	CCO:MP0004238
MGI:1347464	Foxg1	"Fgf8<tm1.1Mrt>/Fgf8<tm1.4Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:1347464	Foxg1	"Fgf8<tm1.1Mrt>/Fgf8<tm1.4Mrt>,Foxg1<tm1M>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003202	abnormal neuron apoptosis	CCO:MP0003202
MGI:1347464	Foxg1	"Dll1<tm1Mjo>/Dll1<tm1Mjo>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:1347464	Foxg1	"Fgf8<tm1.3Mrt>/Fgf8<tm1.4Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004310	small otic vesicle	CCO:MP0004310
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004311	otic vesicle hypoplasia	CCO:MP0004311
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004424	temporal bone hypoplasia	CCO:MP0004424
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:1347464	Foxg1	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003152	abnormal pillar cell differentiation	CCO:MP0003152
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004314	absent vestibule	CCO:MP0004314
MGI:1347464	Foxg1	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003308	abnormal cochlear sensory epithelium morphology	CCO:MP0003308
MGI:1347464	Foxg1	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0003825	abnormal pillar cell morphology	CCO:MP0003825
MGI:1347464	Foxg1	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0004312	absent pillar cells	CCO:MP0004312
MGI:1347464	Foxg1	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0006331	abnormal patterning of the organ of Corti	CCO:MP0006331
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0006286	inner ear hypoplasia	CCO:MP0006286
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0006289	otic capsule hypoplasia	CCO:MP0006289
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004555	pharynx hypoplasia	CCO:MP0004555
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004572	fusion of basioccipital and basisphenoid bone	CCO:MP0004572
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0004900	absent zygomatic arch	CCO:MP0004900
MGI:1347464	Foxg1	"Fgf8<tm1.2Mrt>/Fgf8<tm1.3Mrt>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0001786	skin edema	CCO:MP0001786
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0000111	cleft palate	CCO:MP0000111
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0002116	abnormal craniofacial bone morphology	CCO:MP0002116
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0000680	absent parathyroid glands	CCO:MP0000680
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0000049	abnormal middle ear morphology	CCO:MP0000049
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0006285	absent inner ear	CCO:MP0006285
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0000088	short mandible	CCO:MP0000088
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0003703	abnormal vestibulocochlear ganglion morphology	CCO:MP0003703
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0000040	absent middle ear ossicles	CCO:MP0000040
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0000705	athymia	CCO:MP0000705
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0000036	absent semicircular canals	CCO:MP0000036
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0006031	abnormal branchial pouch morphology	CCO:MP0006031
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0003395	abnormal subclavian artery morphology	CCO:MP0003395
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0003147	absent cochlea	CCO:MP0003147
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0003138	absent tympanic ring	CCO:MP0003138
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0006011	abnormal endolymphatic duct morphology	CCO:MP0006011
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0003056	abnormal hyoid bone morphology	CCO:MP0003056
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0002951	small thyroid gland	CCO:MP0002951
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Tbx1<tm1.1Bem>/Tbx1<tm1.2Bem>"	involves: 129/Sv * C57BL/6 * SJL * Swiss Webster	MP:0005579	absent outer ear	CCO:MP0005579
MGI:1347464	Foxg1	"Bsnd<tm1Tjj>/Bsnd<tm1Tjj>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129/Sv * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0006024	collapsed Reissner membrane	CCO:MP0006024
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Notch1<tm1Grid>/Notch1<tm2Rko>"	involves: 129 * C57BL/6J * Swiss Webster	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:1347464	Foxg1	"Bmp4<tm1Blh>/Bmp4<tm4Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129 * Black Swiss * C57BL/6 * SJL	MP:0006090	abnormal utricle morphology	CCO:MP0006090
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<+>	involves: C57BL/6 * CBA	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	involves: C57BL/6 * CBA	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Notch1<tm1Grid>/Notch1<tm2Rko>"	involves: 129 * C57BL/6J * Swiss Webster	MP:0004497	decreased supporting cell number	CCO:MP0004497
MGI:1347464	Foxg1	"Bsnd<tm1Tjj>/Bsnd<tm1Tjj>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129/Sv * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0008281	abnormal hippocampus size	CCO:MP0008281
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0000832	abnormal thalamus morphology	CCO:MP0000832
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0002756	decreased pyramidal neuron number	CCO:MP0002756
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0004077	abnormal striatum morphology	CCO:MP0004077
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0006254	thin cerebral cortex	CCO:MP0006254
MGI:1347464	Foxg1	"Bsnd<tm1Tjj>/Bsnd<tm1Tjj>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129/Sv * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0001429	dehydration	CCO:MP0001429
MGI:1347464	Foxg1	"Celsr3<tm1Agof>/Celsr3<tm2Agof>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0008128	abnormal brain internal capsule morphology	CCO:MP0008128
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0000783	abnormal forebrain morphology	CCO:MP0000783
MGI:1347464	Foxg1	"Bmp4<tm3Blh>/Bmp4<+>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1347464	Foxg1	"Celsr3<tm1Agof>/Celsr3<tm2Agof>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0008227	absent anterior commissure	CCO:MP0008227
MGI:1347464	Foxg1	"Bmp4<tm1Blh>/Bmp4<tm4Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129 * Black Swiss * C57BL/6 * SJL	MP:0006089	abnormal saccule morphology	CCO:MP0006089
MGI:1347464	Foxg1	"Bmp4<tm1Blh>/Bmp4<tm4Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129 * Black Swiss * C57BL/6 * SJL	MP:0002428	abnormal semicircular canal	CCO:MP0002428
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0000787	abnormal telencephalon morphology	CCO:MP0000787
MGI:1347464	Foxg1	"Bmp4<tm1Blh>/Bmp4<tm4Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129 * Black Swiss * C57BL/6 * SJL	MP:0003169	abnormal scala media morphology	CCO:MP0003169
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	B6.129P2-Foxg1<tm1(cre)Skm>	MP:0000784	forebrain hypoplasia	CCO:MP0000784
MGI:1347464	Foxg1	"Celsr3<tm1Agof>/Celsr3<tm2Agof>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd	MP:0002878	abnormal corticospinal tract morphology	CCO:MP0002878
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Gt(ROSA)26Sor<tm1(RARA*)Soc>/Gt(ROSA)26Sor<tm1(RARA*)Soc>"	involves: 129P2/OlaHsd	MP:0004276	abnormal medial ganglionic eminence morphology	CCO:MP0004276
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Gt(ROSA)26Sor<tm1(RARA*)Soc>/Gt(ROSA)26Sor<tm1(RARA*)Soc>"	involves: 129P2/OlaHsd	MP:0000785	telencephalon hypoplasia	CCO:MP0000785
MGI:1347464	Foxg1	"Six3<tm3Gco>/Six3<tm3Gco>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129S1/Sv * C57BL/6	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:1347464	Foxg1	"Six3<tm3Gco>/Six3<+>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129S1/Sv * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1347464	Foxg1	"Bmp4<tm1Blh>/Bmp4<tm4Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129 * Black Swiss * C57BL/6 * SJL	MP:0008488	abnormal semicircular canal ampulla morphology	CCO:MP0008488
MGI:1347464	Foxg1	"Bmp4<tm1Blh>/Bmp4<tm4Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129 * Black Swiss * C57BL/6 * SJL	MP:0000036	absent semicircular canals	CCO:MP0000036
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:1347464	Foxg1	"Bmp4<tm3Blh>/Bmp4<tm3Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0000443	abnormal snout morphology	CCO:MP0000443
MGI:1347464	Foxg1	"Bmp4<tm3Blh>/Bmp4<tm3Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:1347464	Foxg1	"Bmp4<tm3Blh>/Bmp4<tm3Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0000454	abnormal jaw morphology	CCO:MP0000454
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0001953	respiratory failure	CCO:MP0001953
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0000438	abnormal skull morphology	CCO:MP0000438
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0002233	abnormal nose morphology	CCO:MP0002233
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:1347464	Foxg1	"Foxg1<tm1Lai>/Foxg1<tm1M>,Tg(Foxg1-NHAA)1Lai/0"	involves: 129S1/Sv * C57BL/6	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0006069	abnormal retinal neuronal layer morphology	CCO:MP0006069
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0004274	abnormal embryonic/fetal subventricular zone morphology	CCO:MP0004274
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0008540	abnormal cerebrum morphology	CCO:MP0008540
MGI:1347464	Foxg1	"Foxg1<tm1Lai>/Foxg1<tm1M>,Tg(Foxg1-NHAA)1Lai/0"	involves: 129S1/Sv * C57BL/6	MP:0006007	abnormal basal ganglion morphology	CCO:MP0006007
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Ntf3<tm1Esm>/Ntf3<tm1Esm>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0002741	small olfactory bulb	CCO:MP0002741
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0001404	no spontaneous movement	CCO:MP0001404
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0000787	abnormal telencephalon morphology	CCO:MP0000787
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0000936	small telencephalic vesicles	CCO:MP0000936
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0001575	cyanosis	CCO:MP0001575
MGI:1347464	Foxg1	"Bmp4<tm3Blh>/Bmp4<tm3Blh>,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1347464	Foxg1	Foxg1<tm1M>/Foxg1<tm1M>	involves: 129S1/Sv * C57BL/6J	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Ntf3<tm1Esm>/Ntf3<tm1Esm>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<+>	129(Cg)-Foxg1<tm1(cre)Skm>/J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0002741	small olfactory bulb	CCO:MP0002741
MGI:1347464	Foxg1	Foxg1<tm1(cre)Skm>/Foxg1<tm1(cre)Skm>	129(Cg)-Foxg1<tm1(cre)Skm>/J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0008285	abnormal hippocampus granule cell layer	CCO:MP0008285
MGI:1347464	Foxg1	"Atrx<tm1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: C57BL/6 * FVB/N	MP:0003241	loss of cortex neurons	CCO:MP0003241
MGI:1347464	Foxg1	"Atrx<tm1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: C57BL/6 * FVB/N	MP:0002756	decreased pyramidal neuron number	CCO:MP0002756
MGI:1347464	Foxg1	"Atrx<tm1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: C57BL/6 * FVB/N	MP:0000814	absent dentate gyrus	CCO:MP0000814
MGI:1347464	Foxg1	"Atrx<tm1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: C57BL/6 * FVB/N	MP:0001436	abnormal suckling behavior	CCO:MP0001436
MGI:1347464	Foxg1	"Atrx<tm1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: C57BL/6 * FVB/N	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1347464	Foxg1	"Atrx<tm1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: C57BL/6 * FVB/N	MP:0009703	decreased birth body size	CCO:MP0009703
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:1347464	Foxg1	"Atrx<tm1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: C57BL/6 * FVB/N	MP:0003240	loss of hippocampal neurons	CCO:MP0003240
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0002066	abnormal motor capabilities/coordination/movement	CCO:MP0002066
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Olig2<tm1Qrlu>/Olig2<tm1Qrlu>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0008284	abnormal hippocampus pyramidal cell layer	CCO:MP0008284
MGI:1347464	Foxg1	"Atrx<tm1Pick>/Y,Foxg1<tm1(cre)Skm>/Foxg1<+>"	involves: C57BL/6 * FVB/N	MP:0009546	absent gastric milk in neonates	CCO:MP0009546
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0001177	atelectasis	CCO:MP0001177
MGI:1347464	Foxg1	"Foxg1<tm1(cre)Skm>/Foxg1<+>,Top2b<tm2Jcw>/Top2b<tm2.1Jcw>"	involves: 129S4/SvJae * 129S6/SvEvTac * 129X1/SvJ	MP:0001953	respiratory failure	CCO:MP0001953
MGI:1891915	Foxo4	"Foxo3<tm1.1Rdp>/Foxo3<+>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	MP:0002047	hepatic hemangioma	CCO:MP0002047
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:1891915	Foxo4	"Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	MP:0002627	teratoma	CCO:MP0002627
MGI:1891915	Foxo4	"Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:1891915	Foxo4	"Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1891915	Foxo4	"Foxo3<tm1.1Rdp>/Foxo3<+>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * C57BL/6 * CBA * FVB/N	MP:0002947	hemangioma	CCO:MP0002947
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:1891915	Foxo4	"Foxo3<tm1.1Rdp>/Foxo3<tm1.1Rdp>,Foxo4<tm1.1Rdp>/Foxo4<tm1.1Rdp>"	involves: 129S1/Sv * 129S6/SvEvTac * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0002947	hemangioma	CCO:MP0002947
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1891915	Foxo4	"Foxo1<tm1Rdp>/Foxo1<tm1Rdp>,Foxo3<tm1Rdp>/Foxo3<tm1Rdp>,Foxo4<tm1Rdp>/Foxo4<tm1Rdp>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:1891915	Foxo4	Foxo4<tm1Kca>/Y	involves: 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1891915	Foxo4	Foxo4<tm1Kca>/Foxo4<tm1Kca>	involves: 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0001458	abnormal object recognition memory	CCO:MP0001458
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0004275	abnormal postnatal subventricular zone morphology	CCO:MP0004275
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0004502	decreased incidence of chemically-induced tumors	CCO:MP0004502
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0008014	lung tumor	CCO:MP0008014
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0008019	liver tumor	CCO:MP0008019
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0001714	absent trophoblast giant cells	CCO:MP0001714
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0003708	binucleate	CCO:MP0003708
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0006262	testis tumor	CCO:MP0006262
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0004259	small placenta	CCO:MP0004259
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<tm1.1Mama>	involves: BALB/cJ * C57BL/6 * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<tm1.1Mama>	involves: BALB/cJ * C57BL/6 * SJL	MP:0001715	placental labyrinth hypoplasia	CCO:MP0001715
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<tm1.1Mama>	involves: BALB/cJ * C57BL/6 * SJL	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<tm1.1Mama>	involves: BALB/cJ * C57BL/6 * SJL	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<tm1.1Mama>	involves: BALB/cJ * C57BL/6 * SJL	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<tm1.1Mama>	involves: BALB/cJ * C57BL/6 * SJL	MP:0004266	pale placenta	CCO:MP0004266
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<tm1.1Mama>	involves: BALB/cJ * C57BL/6 * SJL	MP:0008973	decreased erythroid progenitor cell number	CCO:MP0008973
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<+>	involves: 129P2/OlaHsd	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<+>	involves: 129P2/OlaHsd	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:1926790	Fzr1	Fzr1<Gt(RRJ067)Byg>/Fzr1<Gt(RRJ067)Byg>	involves: 129P2/OlaHsd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1926790	Fzr1	Fzr1<tm1.1Mama>/Fzr1<+>	involves: BALB/cJ * C57BL/6 * SJL	MP:0003447	decreased tumor growth/size	CCO:MP0003447
MGI:107799	Gadd45a	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Gadd45b<tm1Daa>/Gadd45b<tm1Daa>,Gadd45g<tm1Mhol>/Gadd45g<tm1Mhol>"	either: (involves: 129X1/SvJ) or (involves: 129P2/OlaHsd * 129X1/SvJ)	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0008499	increased IgG1 level	CCO:MP0008499
MGI:107799	Gadd45a	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:107799	Gadd45a	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:107799	Gadd45a	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0008014	lung tumor	CCO:MP0008014
MGI:107799	Gadd45a	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0002048	lung adenoma	CCO:MP0002048
MGI:107799	Gadd45a	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0004796	increased anti-histone antibody level	CCO:MP0004796
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6 * SKH1) or (involves: 129X1/SvJ * C57BL/6 * SKH1)	MP:0001203	increased sensitivity to skin irradiation	CCO:MP0001203
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6 * SKH1) or (involves: 129X1/SvJ * C57BL/6 * SKH1)	MP:0004501	increased incidence of UV-induced tumors	CCO:MP0004501
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0004771	increased anti-single stranded DNA antibody level	CCO:MP0004771
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005327	abnormal mesangial cell	CCO:MP0005327
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005325	abnormal renal glomerulus morphology	CCO:MP0005325
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0000714	increased thymocyte number	CCO:MP0000714
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004771	increased anti-single stranded DNA antibody level	CCO:MP0004771
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004796	increased anti-histone antibody level	CCO:MP0004796
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004955	increased thymus weight	CCO:MP0004955
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0008499	increased IgG1 level	CCO:MP0008499
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0005012	decreased eosinophil cell number	CCO:MP0005012
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0002494	increased IgM level	CCO:MP0002494
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004759	decreased mitotic index	CCO:MP0004759
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0000914	exencephaly	CCO:MP0000914
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0001204	increased resistance to skin irradiation	CCO:MP0001204
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0002607	decreased basophil cell number	CCO:MP0002607
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0005015	increased T cell number	CCO:MP0005015
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0005160	proteinuria	CCO:MP0005160
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0005327	abnormal mesangial cell	CCO:MP0005327
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0002907	abnormal parturition	CCO:MP0002907
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0003725	increased autoantibody level	CCO:MP0003725
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004024	aneuploidy	CCO:MP0004024
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0004500	increased incidence of ionizing radiation-induced tumors	CCO:MP0004500
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0003725	increased autoantibody level	CCO:MP0003725
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005012	decreased eosinophil cell number	CCO:MP0005012
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002607	decreased basophil cell number	CCO:MP0002607
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0002494	increased IgM level	CCO:MP0002494
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0001828	abnormal T cell activation	CCO:MP0001828
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:107799	Gadd45a	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>"	either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)	MP:0005160	proteinuria	CCO:MP0005160
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:107799	Gadd45a	Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6)	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:107776	Gadd45b	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Gadd45b<tm1Daa>/Gadd45b<tm1Daa>,Gadd45g<tm1Mhol>/Gadd45g<tm1Mhol>"	either: (involves: 129X1/SvJ) or (involves: 129P2/OlaHsd * 129X1/SvJ)	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0008499	increased IgG1 level	CCO:MP0008499
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	B6.129S6-Gadd45b<tm1Flv>	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	B6.129S6-Gadd45b<tm1Flv>	MP:0008566	increased interferon-gamma secretion	CCO:MP0008566
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	B6.129S6-Gadd45b<tm1Flv>	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis	CCO:MP0004799
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	B6.129S6-Gadd45b<tm1Flv>	MP:0005465	abnormal T-helper 1 physiology	CCO:MP0005465
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	B6.129S6-Gadd45b<tm1Flv>	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	B6.129S6-Gadd45b<tm1Flv>	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac	MP:0008088	abnormal T-helper 1 cell differentiation	CCO:MP0008088
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0008049	increased memory T cell number	CCO:MP0008049
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0004796	increased anti-histone antibody level	CCO:MP0004796
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002494	increased IgM level	CCO:MP0002494
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0008210	increased mature B cell number	CCO:MP0008210
MGI:107776	Gadd45b	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0008688	decreased interleukin-2 secretion	CCO:MP0008688
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0008706	decreased interleukin-6 secretion	CCO:MP0008706
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0002376	abnormal dendritic cell physiology	CCO:MP0002376
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0005463	abnormal CD4-positive T cell physiology	CCO:MP0005463
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0005465	abnormal T-helper 1 physiology	CCO:MP0005465
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0005466	abnormal T-helper 2 physiology	CCO:MP0005466
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0008088	abnormal T-helper 1 cell differentiation	CCO:MP0008088
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0008664	decreased interleukin-12 secretion	CCO:MP0008664
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0008700	decreased interleukin-4 secretion	CCO:MP0008700
MGI:107776	Gadd45b	Gadd45b<tm1Flv>/Gadd45b<tm1Flv>	involves: 129S6/SvEvTac	MP:0008567	decreased interferon-gamma secretion	CCO:MP0008567
MGI:107776	Gadd45b	Gadd45b<tm1Daa>/Gadd45b<tm1Daa>	involves: 129X1/SvJ * C57BL/6	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:1346325	Gadd45g	Gadd45g<tm1Mhol>/Gadd45g<tm1Mhol>	involves: 129	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1346325	Gadd45g	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Gadd45b<tm1Daa>/Gadd45b<tm1Daa>,Gadd45g<tm1Mhol>/Gadd45g<tm1Mhol>"	either: (involves: 129X1/SvJ) or (involves: 129P2/OlaHsd * 129X1/SvJ)	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1346325	Gadd45g	Gadd45g<tm1Flv>/Gadd45g<tm1Flv>	involves: 129S1/Sv	MP:0005069	abnormal NK cell physiology	CCO:MP0005069
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002494	increased IgM level	CCO:MP0002494
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0004796	increased anti-histone antibody level	CCO:MP0004796
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0008049	increased memory T cell number	CCO:MP0008049
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0008210	increased mature B cell number	CCO:MP0008210
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0008499	increased IgG1 level	CCO:MP0008499
MGI:1346325	Gadd45g	"Gadd45b<tm1Flv>/Gadd45b<tm1Flv>,Gadd45g<tm1Flv>/Gadd45g<tm1Flv>"	involves: 129S1/Sv * 129S6/SvEvTac	MP:0008088	abnormal T-helper 1 cell differentiation	CCO:MP0008088
MGI:1346325	Gadd45g	Gadd45g<tm1Flv>/Gadd45g<tm1Flv>	involves: 129S1/Sv	MP:0008567	decreased interferon-gamma secretion	CCO:MP0008567
MGI:1346325	Gadd45g	Gadd45g<tm1Flv>/Gadd45g<tm1Flv>	involves: 129S1/Sv	MP:0008088	abnormal T-helper 1 cell differentiation	CCO:MP0008088
MGI:1346325	Gadd45g	Gadd45g<tm1Flv>/Gadd45g<tm1Flv>	involves: 129S1/Sv	MP:0005465	abnormal T-helper 1 physiology	CCO:MP0005465
MGI:1346325	Gadd45g	Gadd45g<tm1Flv>/Gadd45g<tm1Flv>	involves: 129S1/Sv	MP:0002534	type IV hypersensitivity reaction	CCO:MP0002534
MGI:1346325	Gadd45g	Gadd45g<tm1Jni>/Gadd45g<tm1Jni>	involves: 129P2/OlaHsd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0004634	short metacarpal bones	CCO:MP0004634
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0004271	abnormal paw/hand/foot morphology	CCO:MP0004271
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0005650	abnormal limb bud morphology	CCO:MP0005650
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000852	small cerebellum	CCO:MP0000852
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000875	abnormal cerebellar Purkinje cell layer	CCO:MP0000875
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000889	abnormal cerebellar molecular layer	CCO:MP0000889
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0006099	thin granule layer	CCO:MP0006099
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000872	abnormal external granule cell layer morphology	CCO:MP0000872
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0008572	abnormal Purkinje cell dendrite morphology	CCO:MP0008572
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: 129/Sv * C57BL/6J	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: 129/Sv * C57BL/6J	MP:0000565	oligodactyly	CCO:MP0000565
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: 129/Sv * C57BL/6J	MP:0000547	short limbs	CCO:MP0000547
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: 129/Sv * C57BL/6J	MP:0000925	abnormal floor plate morphology	CCO:MP0000925
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000565	oligodactyly	CCO:MP0000565
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002235	abnormal external nares morphology	CCO:MP0002235
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0005157	holoprosencephaly	CCO:MP0005157
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<tm1Chg>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0004635	short metatarsal bones	CCO:MP0004635
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005287	narrow eye opening	CCO:MP0005287
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001312	abnormal cornea morphology	CCO:MP0001312
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001306	small lens	CCO:MP0001306
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001322	abnormal iris morphology	CCO:MP0001322
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002699	abnormal vitreous body	CCO:MP0002699
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005099	abnormal ciliary body morphology	CCO:MP0005099
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005193	abnormal anterior eye segment morphology	CCO:MP0005193
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005195	abnormal posterior eye segment morphology	CCO:MP0005195
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005201	abnormal retinal pigment epithelium morphology	CCO:MP0005201
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001679	thin apical ectodermal ridge	CCO:MP0001679
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005262	coloboma	CCO:MP0005262
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<tm1Chg>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001700	abnormal embryo turning	CCO:MP0001700
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006069	abnormal retinal neuronal layer morphology	CCO:MP0006069
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001406	abnormal gait	CCO:MP0001406
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001525	impaired balance	CCO:MP0001525
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002543	brachyphalangia	CCO:MP0002543
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002544	brachydactyly	CCO:MP0002544
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000564	syndactyly	CCO:MP0000564
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000854	abnormal cerebellum development	CCO:MP0000854
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001324	abnormal eye pigmentation	CCO:MP0001324
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:95655	Gas1	Gas1<tm1Fan>/Gas1<tm1Fan>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005241	abnormal retinal ganglion layer morphology	CCO:MP0005241
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0002233	abnormal nose morphology	CCO:MP0002233
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0004981	decreased neuronal precursor cell number	CCO:MP0004981
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<tm1Chg>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0004173	abnormal intervertebral disk morphology	CCO:MP0004173
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002184	abnormal innervation	CCO:MP0002184
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000925	abnormal floor plate morphology	CCO:MP0000925
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0000564	syndactyly	CCO:MP0000564
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0000030	abnormal tympanic ring morphology	CCO:MP0000030
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0000141	abnormal vertebral body morphology	CCO:MP0000141
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0000925	abnormal floor plate morphology	CCO:MP0000925
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0004418	small parietal bone	CCO:MP0004418
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0004981	decreased neuronal precursor cell number	CCO:MP0004981
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<+>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0000565	oligodactyly	CCO:MP0000565
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<+>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0004980	increased neuronal precursor cell number	CCO:MP0004980
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0000087	absent mandible	CCO:MP0000087
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0000141	abnormal vertebral body morphology	CCO:MP0000141
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0005157	holoprosencephaly	CCO:MP0005157
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0003935	abnormal craniofacial development	CCO:MP0003935
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0004539	absent maxilla	CCO:MP0004539
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0004620	cervical vertebral fusion	CCO:MP0004620
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000141	abnormal vertebral body morphology	CCO:MP0000141
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000565	oligodactyly	CCO:MP0000565
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000088	short mandible	CCO:MP0000088
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0002233	abnormal nose morphology	CCO:MP0002233
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<tm1Chg>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003885	abnormal rostral-caudal body axis extension	CCO:MP0003885
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<+>,Gas1<tm2Fan>/Gas1<tm2Fan>"	involves: 129/Sv * C57BL/6J	MP:0000564	syndactyly	CCO:MP0000564
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<tm1Chg>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000291	enlarged pericardium	CCO:MP0000291
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<tm1Chg>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<tm1Chg>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Gli3<Xt-J>/Gli3<Xt-J>"	involves: 129/Sv * C3H/HeJ * C57BL/6J	MP:0000562	polydactyly	CCO:MP0000562
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0000455	abnormal maxilla morphology	CCO:MP0000455
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0002233	abnormal nose morphology	CCO:MP0002233
MGI:95655	Gas1	Gas1<tm2Fan>/Gas1<tm2Fan>	involves: C57BL/6J	MP:0000565	oligodactyly	CCO:MP0000565
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<+>"	involves: 129/Sv * C57BL/6J	MP:0000141	abnormal vertebral body morphology	CCO:MP0000141
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<+>"	involves: 129/Sv * C57BL/6J	MP:0000564	syndactyly	CCO:MP0000564
MGI:95655	Gas1	"Gas1<tm2Fan>/Gas1<tm2Fan>,Shh<tm1Chg>/Shh<tm1Chg>"	involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000270	abnormal heart tube morphology	CCO:MP0000270
MGI:95655	Gas1	"Cdon<tm2Rsk>/Cdon<tm2Rsk>,Gas1<tm2Fan>/Gas1<+>"	involves: 129/Sv * C57BL/6J	MP:0000565	oligodactyly	CCO:MP0000565
MGI:1927344	Gmnn	Gmnn<Gt(XT0615)Wtsi>/Gmnn<Gt(XT0615)Wtsi>	Not Specified	MP:0004964	absent inner cell mass	CCO:MP0004964
MGI:1927344	Gmnn	Gmnn<Gt(XT0615)Wtsi>/Gmnn<Gt(XT0615)Wtsi>	Not Specified	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1927344	Gmnn	Gmnn<Gt(XT0615)Wtsi>/Gmnn<Gt(XT0615)Wtsi>	Not Specified	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1927344	Gmnn	Gmnn<tm1Nyma>/Gmnn<tm1Nyma>	involves: C57BL/6	MP:0003566	abnormal cell adhesion	CCO:MP0003566
MGI:1927344	Gmnn	Gmnn<Gt(XT0615)Wtsi>/Gmnn<Gt(XT0615)Wtsi>	Not Specified	MP:0005076	abnormal cell differentiation	CCO:MP0005076
MGI:1927344	Gmnn	Gmnn<Gt(XT0615)Wtsi>/Gmnn<Gt(XT0615)Wtsi>	Not Specified	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1927344	Gmnn	Gmnn<tm1Nyma>/Gmnn<tm1Nyma>	involves: C57BL/6	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1927344	Gmnn	Gmnn<tm1Nyma>/Gmnn<tm1Nyma>	involves: C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1927344	Gmnn	Gmnn<tm1Nyma>/Gmnn<tm1Nyma>	involves: C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1927344	Gmnn	Gmnn<tm1Nyma>/Gmnn<tm1Nyma>	involves: C57BL/6	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1927344	Gmnn	Gmnn<Gt(XT0615)Wtsi>/Gmnn<Gt(XT0615)Wtsi>	Not Specified	MP:0005028	abnormal trophectoderm morphology	CCO:MP0005028
MGI:1927344	Gmnn	Gmnn<Gt(XT0615)Wtsi>/Gmnn<Gt(XT0615)Wtsi>	Not Specified	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0004794	increased anti-nuclear antigen antibody level	CCO:MP0004794
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0008499	increased IgG1 level	CCO:MP0008499
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0003945	abnormal lymphocyte physiology	CCO:MP0003945
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:1890220	Gpr132	"Gpr132<tm1Witt>/Gpr132<tm1Witt>,Ldlr<tm1Her>/Ldlr<tm1Her>"	B6.129-Ldlr<tm1Her> Gpr132<tm1Witt>	MP:0002451	abnormal macrophage physiology	CCO:MP0002451
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0005150	cachexia	CCO:MP0005150
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0005154	increased B cell proliferation	CCO:MP0005154
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0009623	enlarged inguinal lymph nodes	CCO:MP0009623
MGI:1890220	Gpr132	"Gpr132<tm1Witt>/Gpr132<tm1Witt>,Ldlr<tm1Her>/Ldlr<tm1Her>"	B6.129-Ldlr<tm1Her> Gpr132<tm1Witt>	MP:0005338	atherosclerotic lesions	CCO:MP0005338
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0002461	increased immunoglobulin level	CCO:MP0002461
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0001860	liver inflammation	CCO:MP0001860
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0001859	kidney inflammation	CCO:MP0001859
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0002339	abnormal lymph node morphology	CCO:MP0002339
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0002722	abnormal immune system organ morphology	CCO:MP0002722
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0002495	increased IgA level	CCO:MP0002495
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	involves: 129X1/SvJ * BALB/c	MP:0001861	lung inflammation	CCO:MP0001861
MGI:1890220	Gpr132	Gpr132<tm1Witt>/Gpr132<tm1Witt>	B6.129X1-Gpr132<tm1Witt>	MP:0003799	impaired macrophage migration	CCO:MP0003799
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0003718	maternal effect	CCO:MP0003718
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0003699	abnormal female reproductive system physiology	CCO:MP0003699
MGI:101908	Gpr3	Gpr3<tm1Dgen>/Gpr3<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	MP:0001973	increased thermal nociceptive threshold	CCO:MP0001973
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0001750	increased circulating follicle stimulating hormone level	CCO:MP0001750
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0001931	abnormal oogenesis	CCO:MP0001931
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0001125	abnormal oocyte morphology	CCO:MP0001125
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0001935	decreased litter size	CCO:MP0001935
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:101908	Gpr3	Gpr3<tm1Cled>/Gpr3<tm1Cled>	either: B6.129-Gpr3<tm1Cled> or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0009007	short estrous cycle	CCO:MP0009007
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Jrw>	involves: 129 * 129S6/SvEvTac * CD-1	MP:0004679	xiphoid process foramen	CCO:MP0004679
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * CD-1	MP:0008277	abnormal sternum ossification	CCO:MP0008277
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * CD-1	MP:0004679	xiphoid process foramen	CCO:MP0004679
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * CD-1	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Jrw>	involves: 129 * 129S6/SvEvTac * CD-1	MP:0008277	abnormal sternum ossification	CCO:MP0008277
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * CD-1	MP:0004320	split sternum	CCO:MP0004320
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Jrw>	involves: 129 * 129S6/SvEvTac * CD-1	MP:0004320	split sternum	CCO:MP0004320
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Jrw>	involves: 129 * 129S6/SvEvTac * CD-1	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Jrw>	involves: 129 * 129S6/SvEvTac * CD-1	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Jrw>	involves: 129 * 129S6/SvEvTac * CD-1	MP:0000111	cleft palate	CCO:MP0000111
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Grc>	involves: 129S6/SvEvTac * CD-1	MP:0008277	abnormal sternum ossification	CCO:MP0008277
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Grc>	involves: 129S6/SvEvTac * CD-1	MP:0004679	xiphoid process foramen	CCO:MP0004679
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Grc>	involves: 129S6/SvEvTac * CD-1	MP:0004320	split sternum	CCO:MP0004320
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Grc>	involves: 129S6/SvEvTac * CD-1	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Grc>	involves: 129S6/SvEvTac * CD-1	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:1861437	Gsk3b	Gsk3b<tm1Grc>/Gsk3b<tm1Grc>	involves: 129S6/SvEvTac * CD-1	MP:0000111	cleft palate	CCO:MP0000111
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * CD-1	MP:0000111	cleft palate	CCO:MP0000111
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * CD-1	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Tph2<tm1Mca>/Tph2<tm1Mca>"	involves: 129 * 129S6/SvEvTac * C57BL/6J	MP:0001360	abnormal social investigation	CCO:MP0001360
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6	MP:0005605	increased bone mass	CCO:MP0005605
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6	MP:0000057	abnormal osteogenesis	CCO:MP0000057
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6	MP:0001533	abnormal skeleton physiology	CCO:MP0001533
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129 * C57BL/6J	MP:0005331	insulin resistance	CCO:MP0005331
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129 * C57BL/6J	MP:0005217	abnormal pancreatic beta cell morphology	CCO:MP0005217
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129 * C57BL/6J	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6	MP:0003796	abnormal cortical bone morphology	CCO:MP0003796
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Insr<tm1Dac>/Insr<+>"	involves: 129 * C57BL/6J	MP:0009114	decreased pancreatic beta cell mass	CCO:MP0009114
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6	MP:0005006	abnormal osteoblast physiology	CCO:MP0005006
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Insr<tm1Dac>/Insr<+>"	involves: 129 * C57BL/6J	MP:0005331	insulin resistance	CCO:MP0005331
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Insr<tm1Dac>/Insr<+>"	involves: 129 * C57BL/6J	MP:0005292	improved glucose tolerance	CCO:MP0005292
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Insr<tm1Dac>/Insr<+>"	involves: 129 * C57BL/6J	MP:0001560	abnormal circulating insulin level	CCO:MP0001560
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Insr<tm1Dac>/Insr<+>"	involves: 129 * C57BL/6J	MP:0000188	abnormal circulating glucose level	CCO:MP0000188
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129 * C57BL/6J	MP:0000188	abnormal circulating glucose level	CCO:MP0000188
MGI:1861437	Gsk3b	"Gsk3b<tm2Jrw>/Gsk3b<tm2Jrw>,Irs2<tm1Mfw>/Irs2<tm1Mfw>,Tg(Ins2-cre)1Herr/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	MP:0000188	abnormal circulating glucose level	CCO:MP0000188
MGI:1861437	Gsk3b	Gsk3b<tm1.1Atak>/Gsk3b<+>	involves: C57BL/6	MP:0008414	abnormal spatial reference memory	CCO:MP0008414
MGI:1861437	Gsk3b	Gsk3b<tm1.1Atak>/Gsk3b<+>	involves: C57BL/6	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:1861437	Gsk3b	Gsk3b<tm1.1Atak>/Gsk3b<+>	involves: C57BL/6	MP:0001449	abnormal learning/ memory	CCO:MP0001449
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6	MP:0000130	abnormal cancellous bone morphology	CCO:MP0000130
MGI:1861437	Gsk3b	"Gsk3b<tm2Jrw>/Gsk3b<tm2Jrw>,Irs2<tm1Mfw>/Irs2<tm1Mfw>,Tg(Ins2-cre)1Herr/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6	MP:0004992	increased bone resorption	CCO:MP0004992
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Runx2<tm1Kish>/Runx2<+>"	involves: 129 * 129P2/OlaHsd * C57BL/6	MP:0005298	abnormal clavicle morphology	CCO:MP0005298
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Runx2<tm1Kish>/Runx2<+>"	involves: 129 * 129P2/OlaHsd * C57BL/6	MP:0000084	abnormal fontanelle morphology	CCO:MP0000084
MGI:1861437	Gsk3b	"Gsk3b<tm1Jrw>/Gsk3b<+>,Irs2<tm1Mfw>/Irs2<tm1Mfw>"	involves: 129 * C57BL/6J	MP:0005559	increased circulating glucose level	CCO:MP0005559
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * C57BL/6J	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * C57BL/6J	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<tm1Jrw>	involves: 129 * C57BL/6J	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6J	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6J	MP:0001417	decreased exploration in new environment	CCO:MP0001417
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6J	MP:0002078	abnormal glucose homeostasis	CCO:MP0002078
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6J	MP:0002573	behavioral despair	CCO:MP0002573
MGI:1861437	Gsk3b	Gsk3b<tm1Jrw>/Gsk3b<+>	involves: 129 * C57BL/6J	MP:0002727	decreased circulating insulin level	CCO:MP0002727
MGI:1861437	Gsk3b	Gsk3b<tm1Dral>/Gsk3b<tm1Dral>	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005438	abnormal glycogen homeostasis	CCO:MP0005438
MGI:1861437	Gsk3b	Gsk3b<tm1Dgen>/Gsk3b<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1861437	Gsk3b	Gsk3b<tm1Dgen>/Gsk3b<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1861437	Gsk3b	"Gsk3a<tm1Dral>/Gsk3a<tm1Dral>,Gsk3b<tm1Dral>/Gsk3b<tm1Dral>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005440	increased glycogen level	CCO:MP0005440
MGI:2176207	H1foo	H1foo<tm1Eya>/H1foo<tm1Eya>	involves: 129S1/Sv * 129X1/SvJ	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:102688	H2afx	"H2afx<tm1Nus>/H2afx<tm2.1Fwa>,Tg(Cdh5-cre)7Mlia/0"	involves: 129S6/SvEvTac * FVB/N	MP:0003711	pathological neovascularization	CCO:MP0003711
MGI:102688	H2afx	"H2afx<tm1Nus>/H2afx<tm2.1Fwa>,Tg(Cdh5-cre)7Mlia/0"	involves: 129S6/SvEvTac * FVB/N	MP:0003447	decreased tumor growth/size	CCO:MP0003447
MGI:102688	H2afx	"H2afx<tm1Nus>/H2afx<tm2.1Fwa>,Tg(Cdh5-cre)7Mlia/0"	involves: 129S6/SvEvTac * FVB/N	MP:0008852	retinal neovascularization	CCO:MP0008852
MGI:102688	H2afx	"H2afx<tm1Fwa>/H2afx<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:102688	H2afx	"H2afx<tm1Fwa>/H2afx<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * C57BL/6	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:102688	H2afx	"H2afx<tm1Fwa>/H2afx<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0001658	increased mortality induced by gamma-irradiation	CCO:MP0001658
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0001147	small testis	CCO:MP0001147
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0003711	pathological neovascularization	CCO:MP0003711
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0003447	decreased tumor growth/size	CCO:MP0003447
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0004816	abnormal class switch recombination	CCO:MP0004816
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0008852	retinal neovascularization	CCO:MP0008852
MGI:102688	H2afx	"H2afx<tm1Nus>/H2afx<tm1Nus>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0003710	abnormal physiological neovascularization	CCO:MP0003710
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0004003	abnormal vascular endothelial cell physiology	CCO:MP0004003
MGI:102688	H2afx	"H2afx<tm1Nus>/H2afx<tm1Nus>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:102688	H2afx	"H2afx<tm1Nus>/H2afx<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:102688	H2afx	"H2afx<tm1Nus>/H2afx<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:102688	H2afx	H2afx<tm1Nus>/H2afx<tm1Nus>	Not Specified	MP:0001805	decreased IgG level	CCO:MP0001805
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0005608	cardiac interstitial fibrosis	CCO:MP0005608
MGI:1343091	Hdac3	Hdac3<tm1.2Eno>/Hdac3<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0002954	abnormal aerobic energy metabolism	CCO:MP0002954
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0002833	increased heart weight	CCO:MP0002833
MGI:1343091	Hdac3	Hdac3<tm1.2Eno>/Hdac3<tm1.2Eno>	involves: 129S/SvEv * C57BL/6	MP:0001695	abnormal gastrulation	CCO:MP0001695
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0005406	abnormal heart size	CCO:MP0005406
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0005598	decreased ventricle muscle contractility	CCO:MP0005598
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0001547	abnormal lipid level	CCO:MP0001547
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0002753	dilated heart left ventricle	CCO:MP0002753
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0005317	increased triglyceride level	CCO:MP0005317
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0001625	cardiac hypertrophy	CCO:MP0001625
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0000603	pale liver	CCO:MP0000603
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0002696	decreased circulating glucagon level	CCO:MP0002696
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0005439	decreased glycogen level	CCO:MP0005439
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0002981	increased liver weight	CCO:MP0002981
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000599	enlarged liver	CCO:MP0000599
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0005178	increased circulating cholesterol level	CCO:MP0005178
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0000599	enlarged liver	CCO:MP0000599
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0001552	increased circulating triglyceride level	CCO:MP0001552
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0000182	increased circulating LDL cholesterol level	CCO:MP0000182
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0003982	increased cholesterol level	CCO:MP0003982
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0002078	abnormal glucose homeostasis	CCO:MP0002078
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0001265	decreased body size	CCO:MP0001265
MGI:1343091	Hdac3	Hdac3<tm1Swh>/Hdac3<tm1.1Swh>	involves: 129S6/SvEvTac * FVB/N	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1343091	Hdac3	Hdac3<tm1Swh>/Hdac3<tm1.1Swh>	involves: 129S6/SvEvTac * FVB/N	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1343091	Hdac3	Hdac3<tm1Swh>/Hdac3<tm1.1Swh>	involves: 129S6/SvEvTac * FVB/N	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0002727	decreased circulating insulin level	CCO:MP0002727
MGI:1343091	Hdac3	Hdac3<tm1.1Swh>/Hdac3<tm1.1Swh>	involves: 129S6/SvEvTac * FVB/N	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0002981	increased liver weight	CCO:MP0002981
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0002941	increased circulating alanine transaminase level	CCO:MP0002941
MGI:1343091	Hdac3	"Hdac3<tm1.1Eno>/Hdac3<tm1.1Eno>,Tg(Myh6-cre)2182Mds/?"	involves: 129S/SvEv * C57BL/6	MP:0006035	abnormal mitochondrial morphology	CCO:MP0006035
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0005454	decreased adipose tissue amount	CCO:MP0005454
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0005439	decreased glycogen level	CCO:MP0005439
MGI:1343091	Hdac3	"Hdac3<tm1Swh>/Hdac3<tm1.1Swh>,Tg(Alb-cre)21Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * DBA	MP:0005317	increased triglyceride level	CCO:MP0005317
MGI:1343091	Hdac3	Hdac3<tm1Swh>/Hdac3<tm1.1Swh>	involves: 129S6/SvEvTac * FVB/N	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000131	abnormal long bone epiphysis morphology	CCO:MP0000131
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000558	abnormal tibia morphology	CCO:MP0000558
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000160	kyphosis	CCO:MP0000160
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000066	osteoporosis	CCO:MP0000066
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0003419	delayed endochondral bone ossification	CCO:MP0003419
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0001406	abnormal gait	CCO:MP0001406
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002989	small kidney	CCO:MP0002989
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0003047	abnormal thoracic vertebrae morphology	CCO:MP0003047
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000063	decreased bone density	CCO:MP0000063
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0001177	atelectasis	CCO:MP0001177
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0009674	decreased birth weight	CCO:MP0009674
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0009431	decreased fetal weight	CCO:MP0009431
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0009429	decreased embryo weight	CCO:MP0009429
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0008844	decreased subcutaneous adipose tissue amount	CCO:MP0008844
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0003109	short femur	CCO:MP0003109
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0003723	abnormal long bone morphology	CCO:MP0003723
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0005150	cachexia	CCO:MP0005150
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0001953	respiratory failure	CCO:MP0001953
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002075	abnormal coat/hair pigmentation	CCO:MP0002075
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000414	alopecia	CCO:MP0000414
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0003786	premature aging	CCO:MP0003786
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002764	short tibia	CCO:MP0002764
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002113	abnormal skeleton development	CCO:MP0002113
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0001242	hyperkeratosis	CCO:MP0001242
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0000706	small thymus	CCO:MP0000706
MGI:106209	Hells	Hells<tm1Rarc>/Hells<tm1Rarc>	involves: 129X1/SvJ * C57BL/6J	MP:0002703	abnormal renal tubule morphology	CCO:MP0002703
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0001262	decreased body weight	CCO:MP0001262
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0000692	small spleen	CCO:MP0000692
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0000706	small thymus	CCO:MP0000706
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0004756	abnormal proximal convoluted tubule morphology	CCO:MP0004756
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0008078	increased CD8-positive T cell number	CCO:MP0008078
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S/SvEv * CZECHII/EiJ	MP:0003123	paternal imprinting	CCO:MP0003123
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:106209	Hells	Hells<tm1Kmu>/Hells<tm1Kmu>	involves: 129S1/Sv	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:103234	Herc2	Herc2<jdf2-8R>/Herc2<jdf2-8R>	Not Specified	MP:0001926	female infertility	CCO:MP0001926
MGI:103234	Herc2	Herc2<jdf2-10R>/Herc2<jdf2-10R>	Not Specified	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:103234	Herc2	Herc2<jdf2-1R>/Herc2<jdf2-1R>	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:103234	Herc2	Herc2<jdf2-9R>/Herc2<jdf2-9R>	Not Specified	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:103234	Herc2	Herc2<jdf2-9R>/Herc2<jdf2-9R>	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:103234	Herc2	Herc2<jdf2-6R>/Herc2<jdf2-6R>	Not Specified	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:103234	Herc2	Herc2<jdf2-5R>/Herc2<jdf2-5R>	Not Specified	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:103234	Herc2	Herc2<jdf2-8R>/Herc2<jdf2-8R>	Not Specified	MP:0004924	abnormal behavior	CCO:MP0004924
MGI:103234	Herc2	Herc2<jdf2-8R>/Herc2<jdf2-8R>	Not Specified	MP:0001925	male infertility	CCO:MP0001925
MGI:103234	Herc2	Herc2<jdf2-10R>/Herc2<jdf2-10R>	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:103234	Herc2	Herc2<jdf2-8R>/Herc2<jdf2-8R>	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:103234	Herc2	Herc2<jdf2-7R>/Herc2<jdf2-7R>	Not Specified	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:103234	Herc2	Herc2<jdf2-4R>/Herc2<jdf2-4R>	Not Specified	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:103234	Herc2	Herc2<jdf2-2R>/Herc2<jdf2-2R>	Not Specified	MP:0004924	abnormal behavior	CCO:MP0004924
MGI:103234	Herc2	Herc2<jdf2-2R>/Herc2<jdf2-2R>	Not Specified	MP:0001925	male infertility	CCO:MP0001925
MGI:103234	Herc2	Herc2<jdf2-2R>/Herc2<jdf2-2R>	Not Specified	MP:0001926	female infertility	CCO:MP0001926
MGI:103234	Herc2	Herc2<jdf2-2R>/Herc2<jdf2-2R>	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:103234	Herc2	Herc2<jdf2-1R>/Herc2<jdf2-1R>	Not Specified	MP:0004924	abnormal behavior	CCO:MP0004924
MGI:103234	Herc2	Herc2<jdf2-1R>/Herc2<jdf2-1R>	Not Specified	MP:0001926	female infertility	CCO:MP0001926
MGI:103234	Herc2	Herc2<jdf2-1R>/Herc2<jdf2-1R>	Not Specified	MP:0001925	male infertility	CCO:MP0001925
MGI:103234	Herc2	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	MP:0001265	decreased body size	CCO:MP0001265
MGI:103234	Herc2	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:103234	Herc2	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:103234	Herc2	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	MP:0002680	decreased corpora lutea number	CCO:MP0002680
MGI:103234	Herc2	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	MP:0002673	abnormal sperm number	CCO:MP0002673
MGI:103234	Herc2	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:103234	Herc2	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	MP:0000745	tremors	CCO:MP0000745
MGI:103234	Herc2	Herc2<J>/Herc2<J>	BALB/cJ-Herc2<J>	MP:0001925	male infertility	CCO:MP0001925
MGI:103234	Herc2	Herc2<jdf2-3R>/Herc2<jdf2-3R>	Not Specified	MP:0004924	abnormal behavior	CCO:MP0004924
MGI:103234	Herc2	Herc2<jdf2-3R>/Herc2<jdf2-3R>	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:103234	Herc2	Herc2<jdf2-3R>/Herc2<jdf2-3R>	Not Specified	MP:0001925	male infertility	CCO:MP0001925
MGI:103234	Herc2	Herc2<jdf2-3R>/Herc2<jdf2-3R>	Not Specified	MP:0001926	female infertility	CCO:MP0001926
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0008489	postnatal slow weight gain	CCO:MP0008489
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0001147	small testis	CCO:MP0001147
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<+>	involves: C57BL/6J * CBA/J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40ACha>	involves: C57BL/6J * CBA/J	MP:0001265	decreased body size	CCO:MP0001265
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40ACha>	involves: C57BL/6J * CBA/J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101761	Hmga2	"Hmga2<tm1Cha>/Hmga2<+>,Lep<ob>/Lep<ob>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40ACha>	involves: C57BL/6J * CBA/J	MP:0000771	abnormal brain size	CCO:MP0000771
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40ACha>	involves: C57BL/6J * CBA/J	MP:0008974	proportional dwarf	CCO:MP0008974
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40BCha>	involves: C57BL/6J * CBA/J	MP:0001265	decreased body size	CCO:MP0001265
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40BCha>	involves: C57BL/6J * CBA/J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40BCha>	involves: C57BL/6J * CBA/J	MP:0008974	proportional dwarf	CCO:MP0008974
MGI:101761	Hmga2	Hmga2<pg-Tg40BCha>/Hmga2<pg-Tg40BCha>	involves: C57BL/6J * CBA/J	MP:0001265	decreased body size	CCO:MP0001265
MGI:101761	Hmga2	Hmga2<pg-Tg40BCha>/Hmga2<pg-Tg40BCha>	involves: C57BL/6J * CBA/J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: MacArthur's small stock	MP:0001265	decreased body size	CCO:MP0001265
MGI:101761	Hmga2	Hmga2<pg-Tg40BCha>/Hmga2<pg-Tg40BCha>	involves: C57BL/6J * CBA/J	MP:0008974	proportional dwarf	CCO:MP0008974
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40ACha>	involves: C57BL/6J * CBA/J	MP:0001147	small testis	CCO:MP0001147
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<+>	involves: C57BL/6J * CBA/J	MP:0001147	small testis	CCO:MP0001147
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<+>	involves: C57BL/6J * CBA/J	MP:0000771	abnormal brain size	CCO:MP0000771
MGI:101761	Hmga2	"Hmga2<tm1Cha>/Hmga2<tm1Cha>,Lep<ob>/Lep<ob>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0009299	decreased mesenteric fat pad weight	CCO:MP0009299
MGI:101761	Hmga2	"Hmga2<tm1Cha>/Hmga2<tm1Cha>,Lep<ob>/Lep<ob>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0009293	decreased inguinal fat pad weight	CCO:MP0009293
MGI:101761	Hmga2	"Hmga2<tm1Cha>/Hmga2<tm1Cha>,Lep<ob>/Lep<ob>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005334	abnormal fat pad morphology	CCO:MP0005334
MGI:101761	Hmga2	"Hmga2<tm1Cha>/Hmga2<tm1Cha>,Lep<ob>/Lep<ob>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:101761	Hmga2	"Hmga2<tm1Cha>/Hmga2<tm1Cha>,Lep<ob>/Lep<ob>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001259	abnormal body weight	CCO:MP0001259
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<+>	involves: C57BL/6J * CBA/J	MP:0002768	small adrenal glands	CCO:MP0002768
MGI:101761	Hmga2	Hmga2<pg-Tg40BCha>/Hmga2<+>	involves: C57BL/6J * CBA/J	MP:0005459	decreased percent body fat	CCO:MP0005459
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0001926	female infertility	CCO:MP0001926
MGI:101761	Hmga2	"Hmga2<tm1Cha>/Hmga2<+>,Lep<ob>/Lep<ob>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:101761	Hmga2	Hmga2<pg-Tg40BCha>/Hmga2<pg-Tg40BCha>	involves: C57BL/6J * CBA/J	MP:0005459	decreased percent body fat	CCO:MP0005459
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0002637	small uterus	CCO:MP0002637
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0003415	priapism	CCO:MP0003415
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0002881	long hair	CCO:MP0002881
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0005448	abnormal energy balance	CCO:MP0005448
MGI:101761	Hmga2	Hmga2<pg-Tg40ACha>/Hmga2<pg-Tg40ACha>	involves: C57BL/6J * CBA/J	MP:0002768	small adrenal glands	CCO:MP0002768
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0002758	long tail	CCO:MP0002758
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: MacArthur's small stock	MP:0001924	infertility	CCO:MP0001924
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0000018	small ears	CCO:MP0000018
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0001925	male infertility	CCO:MP0001925
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0002286	cryptorchism	CCO:MP0002286
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0001127	small ovary	CCO:MP0001127
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0001927	abnormal estrous cycle	CCO:MP0001927
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0001265	decreased body size	CCO:MP0001265
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0002772	brachypodia	CCO:MP0002772
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0002566	abnormal sexual interaction	CCO:MP0002566
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: MacArthur's small stock	MP:0008974	proportional dwarf	CCO:MP0008974
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: MacArthur's small stock	MP:0008489	postnatal slow weight gain	CCO:MP0008489
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: MacArthur's small stock	MP:0005448	abnormal energy balance	CCO:MP0005448
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: A/St * C57BL * MacArthur's small stock	MP:0002089	abnormal postnatal growth/weight/body size	CCO:MP0002089
MGI:101761	Hmga2	Hmga2<pg>/Hmga2<pg>	involves: MacArthur's small stock	MP:0000018	small ears	CCO:MP0000018
MGI:101761	Hmga2	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	MP:0009674	decreased birth weight	CCO:MP0009674
MGI:101761	Hmga2	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	MP:0006378	abnormal spermatogonia morphology	CCO:MP0006378
MGI:101761	Hmga2	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	MP:0000435	shortened head	CCO:MP0000435
MGI:101761	Hmga2	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101761	Hmga2	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	MP:0001925	male infertility	CCO:MP0001925
MGI:101761	Hmga2	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	MP:0005159	azoospermia	CCO:MP0005159
MGI:101761	Hmga2	Hmga2<tm1Cha>/Hmga2<tm1Cha>	involves: 129S7/SvEvBrd	MP:0005659	increased resistance to diet-induced obesity	CCO:MP0005659
MGI:101761	Hmga2	Hmga2<tm1Cha>/Hmga2<+>	involves: 129S7/SvEvBrd	MP:0005659	increased resistance to diet-induced obesity	CCO:MP0005659
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	C.129P2-Hmgb1<tm1Meb>	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * CD-1	MP:0005150	cachexia	CCO:MP0005150
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * CD-1	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * CD-1	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * CD-1	MP:0002083	premature death	CCO:MP0002083
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * BALB/c	MP:0005202	lethargy	CCO:MP0005202
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * BALB/c	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * BALB/c	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * BALB/c	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * BALB/c	MP:0001177	atelectasis	CCO:MP0001177
MGI:96113	Hmgb1	Hmgb1<tm1Meb>/Hmgb1<tm1Meb>	involves: 129P2/OlaHsd * BALB/c	MP:0002715	decreased glycogen catabolism rate	CCO:MP0002715
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000562	polydactyly	CCO:MP0000562
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000572	abnormal autopod morphology	CCO:MP0000572
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<+>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<+>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<+>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000562	polydactyly	CCO:MP0000562
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004641	elongated metatarsal bones	CCO:MP0004641
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<+>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<+>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000572	abnormal autopod morphology	CCO:MP0000572
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004641	elongated metatarsal bones	CCO:MP0004641
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005104	abnormal tarsus morphology	CCO:MP0005104
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0003073	abnormal metacarpal bone morphology	CCO:MP0003073
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0003800	monodactyly	CCO:MP0003800
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0008915	fused carpal bones	CCO:MP0008915
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002187	abnormal fibula morphology	CCO:MP0002187
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000565	oligodactyly	CCO:MP0000565
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005104	abnormal tarsus morphology	CCO:MP0005104
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006253	clinodactyly	CCO:MP0006253
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<+>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004576	abnormal foot plate morphology	CCO:MP0004576
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002187	abnormal fibula morphology	CCO:MP0002187
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000565	oligodactyly	CCO:MP0000565
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005104	abnormal tarsus morphology	CCO:MP0005104
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006253	clinodactyly	CCO:MP0006253
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006279	abnormal limb development	CCO:MP0006279
MGI:96173	Hoxa13	Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004576	abnormal foot plate morphology	CCO:MP0004576
MGI:96173	Hoxa13	Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006279	abnormal limb development	CCO:MP0006279
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000547	short limbs	CCO:MP0000547
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005104	abnormal tarsus morphology	CCO:MP0005104
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004576	abnormal foot plate morphology	CCO:MP0004576
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005104	abnormal tarsus morphology	CCO:MP0005104
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004576	abnormal foot plate morphology	CCO:MP0004576
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002187	abnormal fibula morphology	CCO:MP0002187
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004355	short radius	CCO:MP0004355
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004359	short ulna	CCO:MP0004359
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000572	abnormal autopod morphology	CCO:MP0000572
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002187	abnormal fibula morphology	CCO:MP0002187
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000547	short limbs	CCO:MP0000547
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004355	short radius	CCO:MP0004355
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<tm2Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0004359	short ulna	CCO:MP0004359
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000572	abnormal autopod morphology	CCO:MP0000572
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0003800	monodactyly	CCO:MP0003800
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0005104	abnormal tarsus morphology	CCO:MP0005104
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0008915	fused carpal bones	CCO:MP0008915
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<tm1Ipc>,Hoxd13<tm1Ddu>/Hoxd13<+>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	"Hoxa13<tm2Ipc>/Hoxa13<+>,Hoxd13<tm1Ddu>/Hoxd13<tm1Ddu>"	either: (involves: 129/Sv * 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0003073	abnormal metacarpal bone morphology	CCO:MP0003073
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<spdh>/Hoxd13<spdh>"	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	MP:0002772	brachypodia	CCO:MP0002772
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<spdh>/Hoxd13<spdh>"	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	MP:0008730	fused phalanges	CCO:MP0008730
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<spdh>/Hoxd13<spdh>"	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	MP:0006230	iris stroma hypoplasia	CCO:MP0006230
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<spdh>/Hoxd13<spdh>"	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	MP:0000564	syndactyly	CCO:MP0000564
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<spdh>/Hoxd13<+>"	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	MP:0005230	ectrodactyly	CCO:MP0005230
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<spdh>/Hoxd13<spdh>"	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	MP:0002543	brachyphalangia	CCO:MP0002543
MGI:96173	Hoxa13	"Hoxa13<tm1Ipc>/Hoxa13<+>,Hoxd13<spdh>/Hoxd13<spdh>"	involves: 129S2/SvPas * C3HeB/FeJLe * C57BL/6J	MP:0004271	abnormal paw/hand/foot morphology	CCO:MP0004271
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<+>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0000564	syndactyly	CCO:MP0000564
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	Hoxa13<tm1Mrc>/Hoxa13<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ	MP:0001785	edema	CCO:MP0001785
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0000572	abnormal autopod morphology	CCO:MP0000572
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ	MP:0000492	abnormal rectum morphology	CCO:MP0000492
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0001219	thickened epidermis	CCO:MP0001219
MGI:96173	Hoxa13	"Hoxa13<Hd>/Hoxa13<+>,Tg(Prrx1-Sox9,-lacZ)1Haak/0"	involves: C57BL/6 * DBA/2 * MYA/Hu	MP:0000562	polydactyly	CCO:MP0000562
MGI:96173	Hoxa13	Hoxa13<tm1Mrc>/Hoxa13<tm1Mrc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0003230	abnormal umbilical artery	CCO:MP0003230
MGI:96173	Hoxa13	"Hoxa13<Hd>/Hoxa13<+>,Tg(Prrx1-Sox9,-lacZ)1Haak/0"	involves: C57BL/6 * DBA/2 * MYA/Hu	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ	MP:0001715	placental labyrinth hypoplasia	CCO:MP0001715
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ	MP:0003124	hypospadia	CCO:MP0003124
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ	MP:0003230	abnormal umbilical artery	CCO:MP0003230
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ	MP:0003942	abnormal urinary system development	CCO:MP0003942
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:96173	Hoxa13	Hoxa13<tm1Mrc>/Hoxa13<tm1Mrc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96173	Hoxa13	Hoxa13<tm1.1Mrc>/Hoxa13<tm1.1Mrc>	involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6	MP:0000564	syndactyly	CCO:MP0000564
MGI:96173	Hoxa13	"Hoxa13<Hd>/Hoxa13<+>,Tg(Prrx1-Sox9,-lacZ)1Haak/0"	involves: C57BL/6 * DBA/2 * MYA/Hu	MP:0009049	abnormal hallux morphology	CCO:MP0009049
MGI:96173	Hoxa13	Hoxa13<tm1Mrc>/Hoxa13<tm1Mrc>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003230	abnormal umbilical artery	CCO:MP0003230
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0009087	dilated uterine horn	CCO:MP0009087
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0000666	decreased prostate duct number	CCO:MP0000666
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0000554	abnormal carpal bone morphology	CCO:MP0000554
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0003593	urethrovaginal fistula	CCO:MP0003593
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0001924	infertility	CCO:MP0001924
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:96173	Hoxa13	Hoxa13<tm1Jwi>/Hoxa13<+>	involves: 129S7/SvEvBrd	MP:0000564	syndactyly	CCO:MP0000564
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0009252	absent urinary bladder	CCO:MP0009252
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0009227	cervix hypoplasia	CCO:MP0009227
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0009104	small penile bone	CCO:MP0009104
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0003550	short perineum	CCO:MP0003550
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0008983	small vagina	CCO:MP0008983
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0001265	decreased body size	CCO:MP0001265
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0003675	kidney cysts	CCO:MP0003675
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0003617	urinary bladder hypoplasia	CCO:MP0003617
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0009103	abnormal penile bone morphology	CCO:MP0009103
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0002774	small prostate	CCO:MP0002774
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0000519	hydronephrosis	CCO:MP0000519
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	involves: MYA/Hu	MP:0009001	absent hallux	CCO:MP0009001
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0003446	renal hypoplasia	CCO:MP0003446
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0001926	female infertility	CCO:MP0001926
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0001135	abnormal cervix morphology	CCO:MP0001135
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0000537	abnormal urethra morphology	CCO:MP0000537
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	involves: MYA/Hu	MP:0000564	syndactyly	CCO:MP0000564
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0000516	abnormal urinary system morphology	CCO:MP0000516
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	involves: MYA/Hu	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0001135	abnormal cervix morphology	CCO:MP0001135
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0001157	small seminal gland	CCO:MP0001157
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0000661	small ventral prostate	CCO:MP0000661
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0000653	abnormal sex gland morphology	CCO:MP0000653
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0002059	abnormal seminal gland morphology	CCO:MP0002059
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0001163	abnormal coagulating gland morphology	CCO:MP0001163
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0000538	abnormal urinary bladder morphology	CCO:MP0000538
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0001925	male infertility	CCO:MP0001925
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	B6C3Fe-a/a Hoxa13<Hd> Mcoln3<Va-J>/J	MP:0003270	intestinal obstruction	CCO:MP0003270
MGI:96173	Hoxa13	Hoxa13<tm1Jwi>/Hoxa13<+>	involves: 129S7/SvEvBrd	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	Hoxa13<tm1Jwi>/Hoxa13<tm1Jwi>	involves: 129S7/SvEvBrd	MP:0000565	oligodactyly	CCO:MP0000565
MGI:96173	Hoxa13	Hoxa13<tm1Jwi>/Hoxa13<tm1Jwi>	involves: 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0005230	ectrodactyly	CCO:MP0005230
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0003073	abnormal metacarpal bone morphology	CCO:MP0003073
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0003072	abnormal metatarsal bone morphology	CCO:MP0003072
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0003800	monodactyly	CCO:MP0003800
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	involves: MYA/Hu	MP:0002544	brachydactyly	CCO:MP0002544
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<+>	involves: MYA/Hu	MP:0000565	oligodactyly	CCO:MP0000565
MGI:96173	Hoxa13	Hoxa13<Hd>/Hoxa13<Hd>	involves: MYA/Hu	MP:0005104	abnormal tarsus morphology	CCO:MP0005104
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000627	abnormal mammary gland morphology	CCO:MP0000627
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0009551	urinary bladder transitional cell carcinoma	CCO:MP0009551
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0008000	ovary tumor	CCO:MP0008000
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002018	malignant tumors	CCO:MP0002018
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002039	neuroblastoma	CCO:MP0002039
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003570	uterus leiomyoma	CCO:MP0003570
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<tm1Hx>	involves: 129P2/OlaHsd * C57BL/6J	MP:0009311	duodenum adenocarcinoma	CCO:MP0009311
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002018	malignant tumors	CCO:MP0002018
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:1859271	Htatip2	Htatip2<tm1Hx>/Htatip2<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm2Rsw>	involves: 129S6/SvEvTac * C57BL/6	MP:0004030	induced chromosome breakage	CCO:MP0004030
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm2Rsw>	involves: 129S6/SvEvTac * C57BL/6	MP:0003674	oxidative stress	CCO:MP0003674
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm2Rsw>	involves: 129S6/SvEvTac * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm2Rsw>	involves: 129S6/SvEvTac * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm2Rsw>	involves: 129S6/SvEvTac * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm2Rsw>	involves: 129S6/SvEvTac * C57BL/6	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm2Rsw>	involves: 129S6/SvEvTac * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0009657	failure of chorioallantoic fusion	CCO:MP0009657
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0001726	abnormal allantois morphology	CCO:MP0001726
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0001691	abnormal somite shape	CCO:MP0001691
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0003396	abnormal embryonic hematopoiesis	CCO:MP0003396
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0003400	kinked neural tube	CCO:MP0003400
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0004180	failure of initiation of embryo turning	CCO:MP0004180
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0004573	absent limb buds	CCO:MP0004573
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss)	MP:0000928	incomplete cephalic closure	CCO:MP0000928
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0001700	abnormal embryo turning	CCO:MP0001700
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0000928	incomplete cephalic closure	CCO:MP0000928
MGI:1277962	Hus1	"Hus1<tm1Led>/Hus1<tm1Rsw>,Tg(Hsp70-1-cre)1Arge/0"	involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * CBA	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1277962	Hus1	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Hus1<tm1Led>/Hus1<tm1Led>"	involves: 129S6/SvEvTac	MP:0008410	increased cellular sensitivity to ultraviolet irradiation	CCO:MP0008410
MGI:1277962	Hus1	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Hus1<tm1Led>/Hus1<tm1Led>"	involves: 129S6/SvEvTac	MP:0008409	increased cellular sensitivity to hydroxyurea	CCO:MP0008409
MGI:1277962	Hus1	"Cdkn1a<tm1Led>/Cdkn1a<tm1Led>,Hus1<tm1Led>/Hus1<tm1Led>"	involves: 129S6/SvEvTac	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	involves: 129S6/SvEvTac	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	involves: 129S6/SvEvTac	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	involves: 129S6/SvEvTac	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	involves: 129S6/SvEvTac	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:1277962	Hus1	Hus1<tm1Led>/Hus1<tm1Led>	involves: 129S6/SvEvTac	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0009657	failure of chorioallantoic fusion	CCO:MP0009657
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0003400	kinked neural tube	CCO:MP0003400
MGI:1277962	Hus1	Hus1<tm1.1Rsw>/Hus1<tm1.1Rsw>	involves: 129S4/SvJaeSor * 129S6/SvEvTac	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:99414	Id4	Id4<tm1Mais>/Id4<tm1Mais>	involves: 129X1/SvJ * C57BL/6	MP:0001402	hypoactivity	CCO:MP0001402
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0000913	abnormal brain development	CCO:MP0000913
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0003424	premature neuronal precursor differentiation	CCO:MP0003424
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0000774	decreased brain size	CCO:MP0000774
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0008547	abnormal neocortex morphology	CCO:MP0008547
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0004276	abnormal medial ganglionic eminence morphology	CCO:MP0004276
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0001263	weight loss	CCO:MP0001263
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0004277	abnormal lateral ganglionic eminence morphology	CCO:MP0004277
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0003232	abnormal forebrain development	CCO:MP0003232
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0006007	abnormal basal ganglion morphology	CCO:MP0006007
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0000808	abnormal hippocampus development	CCO:MP0000808
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0000790	abnormal stratification in cerebral cortex	CCO:MP0000790
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0000823	abnormal lateral ventricle morphology	CCO:MP0000823
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0002182	abnormal astrocyte morphology	CCO:MP0002182
MGI:99414	Id4	Id4<tm1Fsky>/Id4<tm1Fsky>	involves: 129P2/OlaHsd * CD-1	MP:0002083	premature death	CCO:MP0002083
MGI:99414	Id4	Id4<tm1Mais>/Id4<tm1Mais>	involves: 129X1/SvJ	MP:0000787	abnormal telencephalon morphology	CCO:MP0000787
MGI:99414	Id4	Id4<tm1Mais>/Id4<tm1Mais>	involves: 129X1/SvJ	MP:0000823	abnormal lateral ventricle morphology	CCO:MP0000823
MGI:99414	Id4	Id4<tm1Mais>/Id4<tm1Mais>	involves: 129X1/SvJ	MP:0000785	telencephalon hypoplasia	CCO:MP0000785
MGI:99414	Id4	Id4<tm1Mais>/Id4<tm1Mais>	involves: 129X1/SvJ	MP:0000808	abnormal hippocampus development	CCO:MP0000808
MGI:99414	Id4	Id4<tm1Mais>/Id4<tm1Mais>	involves: 129X1/SvJ	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:99414	Id4	Id4<tm1Mais>/Id4<tm1Mais>	involves: 129X1/SvJ	MP:0008547	abnormal neocortex morphology	CCO:MP0008547
MGI:99414	Id4	Id4<tm1Mais>/Id4<tm1Mais>	involves: 129X1/SvJ	MP:0000774	decreased brain size	CCO:MP0000774
MGI:1313288	Incenp	Incenp<tm1Khac>/Incenp<tm1Khac>	involves: 129P2/OlaHsd * C57BL/6	MP:0002663	failure to form blastocele	CCO:MP0002663
MGI:1313288	Incenp	Incenp<tm1Khac>/Incenp<tm1Khac>	involves: 129P2/OlaHsd * C57BL/6	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:1313288	Incenp	Incenp<tm1Khac>/Incenp<tm1Khac>	involves: 129P2/OlaHsd * C57BL/6	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:1313288	Incenp	Incenp<tm1Khac>/Incenp<tm1Khac>	involves: 129P2/OlaHsd * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1313288	Incenp	Incenp<tm1Khac>/Incenp<tm1Khac>	involves: 129P2/OlaHsd * C57BL/6	MP:0004964	absent inner cell mass	CCO:MP0004964
MGI:1349481	Ing1	Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1349481	Ing1	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1349481	Ing1	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1349481	Ing1	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	MP:0001658	increased mortality induced by gamma-irradiation	CCO:MP0001658
MGI:1349481	Ing1	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1349481	Ing1	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	MP:0008410	increased cellular sensitivity to ultraviolet irradiation	CCO:MP0008410
MGI:1349481	Ing1	Ing1<Gt(OST206270)Lex>/Ing1<+>	involves: 129S5/SvEvBrd * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1349481	Ing1	"Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1349481	Ing1	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1349481	Ing1	Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1349481	Ing1	"Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1349481	Ing1	Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1349481	Ing1	Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1349481	Ing1	Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1349481	Ing1	Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1349481	Ing1	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	MP:0001386	abnormal maternal nurturing	CCO:MP0001386
MGI:1349481	Ing1	Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>	involves: 129S5/SvEvBrd * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1349481	Ing1	Ing1<tm1Avg>/Ing1<tm1Avg>	involves: 129S1/Sv * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1349481	Ing1	Ing1<Gt(F066C08)Irpa>/Ing1<Gt(F066C08)Irpa>	involves: 129S2/SvPas	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1349481	Ing1	Ing1<Gt(F066C08)Irpa>/Ing1<Gt(F066C08)Irpa>	involves: 129S2/SvPas	MP:0008009	delayed cellular replicative senescence	CCO:MP0008009
MGI:96610	Itgb1	Itgb1<tm1Mlkn>/Itgb1<tm1Mlkn>	involves: 129/Sv * C57BL/6 * SJL	MP:0004964	absent inner cell mass	CCO:MP0004964
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:96610	Itgb1	Itgb1<tm1Mlkn>/Itgb1<tm1Mlkn>	involves: 129/Sv * C57BL/6 * SJL	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:96610	Itgb1	Itgb1<tm1.1Efu>/Itgb1<tm1.1Efu>	involves: 129X1/SvJ	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:96610	Itgb1	Itgb1<tm1.1Efu>/Itgb1<tm1.1Efu>	involves: 129X1/SvJ	MP:0004964	absent inner cell mass	CCO:MP0004964
MGI:96610	Itgb1	Itgb1<tm2Mlkn>/Itgb1<tm2Mlkn>	involves: 129/Sv * C57BL/6 * SJL	MP:0005464	abnormal platelet physiology	CCO:MP0005464
MGI:96610	Itgb1	"Itgb1<tm3Mlkn>/Itgb1<tm3Mlkn>,Tg(Mx1-cre)1Cgn/0"	involves: 129/Sv * C57BL/6 * CBA	MP:0005664	decreased circulating noradrenaline level	CCO:MP0005664
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0001046	abnormal enteric neuron morphology	CCO:MP0001046
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0002926	aganglionic megacolon	CCO:MP0002926
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0002950	abnormal neural crest cell migration	CCO:MP0002950
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0002949	abnormal neural crest cells	CCO:MP0002949
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0002184	abnormal innervation	CCO:MP0002184
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0000864	abnormal vermis morphology	CCO:MP0000864
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0002791	steatorrhea	CCO:MP0002791
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0001393	ataxia	CCO:MP0001393
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0000854	abnormal cerebellum development	CCO:MP0000854
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0000952	abnormal CNS glial cell morphology	CCO:MP0000952
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0001299	abnormal eye distance/ position	CCO:MP0001299
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0000792	abnormal cortical marginal zone morphology	CCO:MP0000792
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0000479	abnormal enterocyte morphology	CCO:MP0000479
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0000852	small cerebellum	CCO:MP0000852
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0005623	abnormal meninges morphology	CCO:MP0005623
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0008030	abnormal Cajal-Retzius cell morphology	CCO:MP0008030
MGI:96610	Itgb1	Itgb1<tm1Son>/Itgb1<tm1Son>	either: 129P2/OlaHsd-Itgb1<tm1Son> or (involves: 129P2/OlaHsd * FVB)	MP:0001544	abnormal cardiovascular system physiology	CCO:MP0001544
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0000432	abnormal head morphology	CCO:MP0000432
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0000458	abnormal mandible morphology	CCO:MP0000458
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0001340	abnormal eyelid morphology	CCO:MP0001340
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: 129X1/SvJ * C57BL/6 * SJL	MP:0000849	abnormal cerebellum morphology	CCO:MP0000849
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000914	exencephaly	CCO:MP0000914
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000930	wavy neural tube	CCO:MP0000930
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001914	hemorrhage	CCO:MP0001914
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0005312	pericardial effusion	CCO:MP0005312
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0000489	abnormal large intestine morphology	CCO:MP0000489
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0003400	kinked neural tube	CCO:MP0003400
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0000488	abnormal intestinal epithelium morphology	CCO:MP0000488
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0003794	delayed somite formation	CCO:MP0003794
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0006301	abnormal mesenchyme morphology	CCO:MP0006301
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0009657	failure of chorioallantoic fusion	CCO:MP0009657
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0000490	abnormal crypts of Lieberkuhn morphology	CCO:MP0000490
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0001262	decreased body weight	CCO:MP0001262
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0001666	abnormal nutrient absorption	CCO:MP0001666
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0001706	abnormal left-right axis patterning	CCO:MP0001706
MGI:96610	Itgb1	Itgb1<tm1Ehi>/Itgb1<tm1Ehi>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0003717	pallor	CCO:MP0003717
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0001258	decreased body length	CCO:MP0001258
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0000759	abnormal skeletal muscle morphology	CCO:MP0000759
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0000929	open neural tube	CCO:MP0000929
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0001575	cyanosis	CCO:MP0001575
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0002884	abnormal branchial arch morphology	CCO:MP0002884
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0004174	abnormal spine curvature	CCO:MP0004174
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0004819	decreased skeletal muscle mass	CCO:MP0004819
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0009406	decreased skeletal muscle fiber number	CCO:MP0009406
MGI:96610	Itgb1	"Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(MMTV-cre)7Mul/0,Tg(MMTV-PyVT)634Mul/0"	involves: FVB/N	MP:0005512	increased resistance to mammary neoplasm	CCO:MP0005512
MGI:96610	Itgb1	"Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Wap-cre)1Gsc/0"	involves: FVB/N	MP:0000627	abnormal mammary gland morphology	CCO:MP0000627
MGI:96610	Itgb1	"Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Wap-cre)1Gsc/0"	involves: FVB/N	MP:0006270	abnormal mammary gland growth during lactation	CCO:MP0006270
MGI:96610	Itgb1	"Cdkn1a<tm1Tyj>/Cdkn1a<tm1Tyj>,Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Wap-cre)1Gsc/0"	involves: 129S2/SvPas * C57BL/6 * FVB/N	MP:0006270	abnormal mammary gland growth during lactation	CCO:MP0006270
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0003400	kinked neural tube	CCO:MP0003400
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0001577	anemia	CCO:MP0001577
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0000930	wavy neural tube	CCO:MP0000930
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0001914	hemorrhage	CCO:MP0001914
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0000841	abnormal hindbrain morphology	CCO:MP0000841
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0000820	abnormal choroid plexus morphology	CCO:MP0000820
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0002639	micrognathia	CCO:MP0002639
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0003054	spina bifida	CCO:MP0003054
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0003091	abnormal cell migration	CCO:MP0003091
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0003400	kinked neural tube	CCO:MP0003400
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0003566	abnormal cell adhesion	CCO:MP0003566
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0000729	abnormal myogenesis	CCO:MP0000729
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0001504	abnormal posture	CCO:MP0001504
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0003743	abnormal facial morphology	CCO:MP0003743
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0006280	abnormal digit development	CCO:MP0006280
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0004261	abnormal embryonic neuroepithelium morphology	CCO:MP0004261
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0006337	abnormal first branchial arch morphology	CCO:MP0006337
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0006341	small first branchial arch	CCO:MP0006341
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0006344	small second branchial arch	CCO:MP0006344
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0000432	abnormal head morphology	CCO:MP0000432
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	FVB.129P2-Itgb1<tm2Son>	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:96610	Itgb1	Itgb1<tm2Son>/Itgb1<tm2Son>	either: 129P2/OlaHsd-Itgb1<tm2Son> or (involves: 129P2/OlaHsd * FVB)	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?,Tg(RIP1-Tag)2Dh/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA * DBA/2J	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Cryaa-cre)10Mlr/?"	involves: 129X1/SvJ * C57BL/6	MP:0001297	microphthalmia	CCO:MP0001297
MGI:96610	Itgb1	"Itgb1<tm4Ref>/Itgb1<tm4Ref>,Tg(Ins2-cre)1Heed/?,Tg(RIP1-Tag)2Dh/?"	involves: C57BL/6 * C57BL/6J * CBA * DBA/2J	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(RIP1-Tag)2Dh/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Cryaa-cre)10Mlr/?"	involves: 129X1/SvJ * C57BL/6	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Cryaa-cre)10Mlr/?"	involves: 129X1/SvJ * C57BL/6	MP:0003078	aphakia	CCO:MP0003078
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Cryaa-cre)10Mlr/?"	involves: 129X1/SvJ * C57BL/6	MP:0003237	abnormal lens epithelium morphology	CCO:MP0003237
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?,Tg(RIP1-Tag)2Dh/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA * DBA/2J	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?,Tg(RIP1-Tag)2Dh/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA * DBA/2J	MP:0003566	abnormal cell adhesion	CCO:MP0003566
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?,Tg(RIP1-Tag)2Dh/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA * DBA/2J	MP:0001273	decreased metastatic potential	CCO:MP0001273
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?,Tg(RIP1-Tag)2Dh/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA * DBA/2J	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?,Tg(RIP1-Tag)2Dh/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA * DBA/2J	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?"	involves: 129 * C57BL/6 * CBA	MP:0009254	disorganized pancreatic islets	CCO:MP0009254
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(Vil-cre)997Gum/0"	involves: 129X1/SvJ * C57BL/6J * SJL	MP:0003949	abnormal circulating lipid level	CCO:MP0003949
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?"	involves: 129 * C57BL/6 * CBA	MP:0009176	increased pancreatic alpha cell number	CCO:MP0009176
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Ins2-cre)1Heed/?,Tg(RIP1-Tag)2Dh/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA * DBA/2J	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000111	cleft palate	CCO:MP0000111
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002657	chondrodystrophy	CCO:MP0002657
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001954	respiratory distress	CCO:MP0001954
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000167	decreased chondrocyte cell number	CCO:MP0000167
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000165	abnormal long bone hypertrophic chondrocyte zone	CCO:MP0000165
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001258	decreased body length	CCO:MP0001258
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002427	disproportionate dwarf	CCO:MP0002427
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004867	decreased platelet calcium level	CCO:MP0004867
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005464	abnormal platelet physiology	CCO:MP0005464
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002764	short tibia	CCO:MP0002764
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000164	abnormal cartilage development	CCO:MP0000164
MGI:96610	Itgb1	Itgb1<tm1Lscd>/Itgb1<tm1Lscd>	involves: 129X1/SvJ * Black Swiss	MP:0001724	abnormal extraembryonic endoderm formation	CCO:MP0001724
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002764	short tibia	CCO:MP0002764
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0003055	abnormal long bone epiphyseal plate morphology	CCO:MP0003055
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004351	short humerus	CCO:MP0004351
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004686	decreased length of long bones	CCO:MP0004686
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001954	respiratory distress	CCO:MP0001954
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0008271	abnormal bone ossification	CCO:MP0008271
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002657	chondrodystrophy	CCO:MP0002657
MGI:96610	Itgb1	Itgb1<tm1Lscd>/Itgb1<tm1Lscd>	involves: 129X1/SvJ * Black Swiss	MP:0005031	abnormal trophoblast layer morphology	CCO:MP0005031
MGI:96610	Itgb1	Itgb1<tm1Lscd>/Itgb1<tm1Lscd>	involves: 129X1/SvJ * Black Swiss	MP:0004963	abnormal blastocoele morphology	CCO:MP0004963
MGI:96610	Itgb1	Itgb1<tm1Lscd>/Itgb1<tm1Lscd>	involves: 129X1/SvJ * Black Swiss	MP:0004965	inner cell mass degeneration	CCO:MP0004965
MGI:96610	Itgb1	Itgb1<tm1Lscd>/Itgb1<tm1Lscd>	involves: 129X1/SvJ * Black Swiss	MP:0008527	embryonic lethality at implantation	CCO:MP0008527
MGI:96610	Itgb1	"Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: C57BL/6 * SJL	MP:0002741	small olfactory bulb	CCO:MP0002741
MGI:96610	Itgb1	"Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: C57BL/6 * SJL	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:96610	Itgb1	"Itgb1<tm1Mll>/Itgb1<tm1Mll>,Tg(Nes-cre)1Kln/0"	involves: C57BL/6 * SJL	MP:0004279	abnormal rostral migratory stream morphology	CCO:MP0004279
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0008151	increased diameter of long bones	CCO:MP0008151
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000164	abnormal cartilage development	CCO:MP0000164
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0003055	abnormal long bone epiphyseal plate morphology	CCO:MP0003055
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004351	short humerus	CCO:MP0004351
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0004686	decreased length of long bones	CCO:MP0004686
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0008151	increased diameter of long bones	CCO:MP0008151
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm2Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0008271	abnormal bone ossification	CCO:MP0008271
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002427	disproportionate dwarf	CCO:MP0002427
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000167	decreased chondrocyte cell number	CCO:MP0000167
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001258	decreased body length	CCO:MP0001258
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000165	abnormal long bone hypertrophic chondrocyte zone	CCO:MP0000165
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(Col2a1-cre)1Asz/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000111	cleft palate	CCO:MP0000111
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm5.1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0009584	decreased keratinocyte proliferation	CCO:MP0009584
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000414	alopecia	CCO:MP0000414
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001406	abnormal gait	CCO:MP0001406
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001924	infertility	CCO:MP0001924
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000379	decreased hair follicle number	CCO:MP0000379
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001190	reddish skin	CCO:MP0001190
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001243	abnormal dermal layer morphology	CCO:MP0001243
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000648	absent sebaceous gland	CCO:MP0000648
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000377	abnormal hair follicle morphology	CCO:MP0000377
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm5.1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0009385	abnormal dermal pigmentation	CCO:MP0009385
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000468	abnormal esophageal epithelium morphology	CCO:MP0000468
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0009004	progressive hair loss	CCO:MP0009004
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0002083	premature death	CCO:MP0002083
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001231	abnormal epidermis stratum basale morphology	CCO:MP0001231
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001222	epidermal hyperplasia	CCO:MP0001222
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001219	thickened epidermis	CCO:MP0001219
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001208	blistering	CCO:MP0001208
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001212	skin lesions	CCO:MP0001212
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001198	tight skin	CCO:MP0001198
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000023	abnormal ear distance/ position	CCO:MP0000023
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000022	abnormal ear shape	CCO:MP0000022
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0005035	perianal ulceration	CCO:MP0005035
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm5.1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0009004	progressive hair loss	CCO:MP0009004
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0004947	skin inflammation	CCO:MP0004947
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0002655	abnormal keratinocyte morphology	CCO:MP0002655
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0009385	abnormal dermal pigmentation	CCO:MP0009385
MGI:96610	Itgb1	Itgb1<tm3Ref>/Itgb1<tm3Ref>	involves: 129S1/Sv * 129X1/SvJ	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0005408	hypopigmentation	CCO:MP0005408
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm5.1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001208	blistering	CCO:MP0001208
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm5.1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000416	sparse hair	CCO:MP0000416
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm5.1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0001243	abnormal dermal layer morphology	CCO:MP0001243
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm5.1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000377	abnormal hair follicle morphology	CCO:MP0000377
MGI:96610	Itgb1	Itgb1<tm5.1Ref>/Itgb1<tm5.1Ref>	involves: 129S1/Sv * 129X1/SvJ	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm5.1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0000386	abnormal hair follicle root sheath	CCO:MP0000386
MGI:96610	Itgb1	"Itgb1<tm1Ref>/Itgb1<tm1Ref>,Tg(KRT1-5-cre)5132Jlj/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J	MP:0002796	impaired skin barrier function	CCO:MP0002796
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0000278	abnormal myocardial fiber morphology	CCO:MP0000278
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0008725	enlarged heart atrium	CCO:MP0008725
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0005598	decreased ventricle muscle contractility	CCO:MP0005598
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0002953	thick ventricular wall	CCO:MP0002953
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0001218	thin epidermis	CCO:MP0001218
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0006138	congestive heart failure	CCO:MP0006138
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0004039	abnormal cardiac cell glucose uptake	CCO:MP0004039
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0004084	abnormal cardiac muscle relaxation	CCO:MP0004084
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0002753	dilated heart left ventricle	CCO:MP0002753
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0004937	dilated heart	CCO:MP0004937
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0005329	abnormal cardiac muscle morphology	CCO:MP0005329
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0002132	abnormal respiratory system morphology	CCO:MP0002132
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0003141	cardiac fibrosis	CCO:MP0003141
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0001855	atrial thrombosis	CCO:MP0001855
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0002754	dilated heart right ventricle	CCO:MP0002754
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0005294	abnormal heart ventricle morphology	CCO:MP0005294
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0004485	increased response of heart to induced stress	CCO:MP0004485
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:96610	Itgb1	"Itgb1<tm1Ross>/Itgb1<tm1Ross>,Myl2<tm1(cre)Krc>/Myl2<+>"	involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss	MP:0002795	dilated cardiomyopathy	CCO:MP0002795
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0004272	abnormal basement membrane morphology	CCO:MP0004272
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0000379	decreased hair follicle number	CCO:MP0000379
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0003704	abnormal hair follicle development	CCO:MP0003704
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0001199	thin skin	CCO:MP0001199
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0001208	blistering	CCO:MP0001208
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0001231	abnormal epidermis stratum basale morphology	CCO:MP0001231
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:96610	Itgb1	"Itgb1<tm1Efu>/Itgb1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	involves: 129X1/SvJ	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0001056	abnormal cranial nerve morphology	CCO:MP0001056
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0002651	abnormal sciatic nerve	CCO:MP0002651
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0001053	abnormal neuromuscular synapse morphology	CCO:MP0001053
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0001052	abnormal muscle innervation	CCO:MP0001052
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0001109	absent Schwann cell precursors	CCO:MP0001109
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0000748	progressive muscle weakness	CCO:MP0000748
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0002269	muscular atrophy	CCO:MP0002269
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:96610	Itgb1	"Itgb1<tm1Lscd>/Itgb1<tm1Ref>,Tg(PLAT-cre)116Sdu/0"	Not Specified	MP:0002083	premature death	CCO:MP0002083
MGI:1341886	Jub	Jub<tm1Gdl>/Jub<tm1Gdl>	involves: 129X1/SvJ * C57BL/6	MP:0003091	abnormal cell migration	CCO:MP0003091
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0001654	hepatic necrosis	CCO:MP0001654
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000596	abnormal liver development	CCO:MP0000596
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0003887	increased hepatocyte apoptosis	CCO:MP0003887
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0002929	abnormal bile duct development	CCO:MP0002929
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0001785	edema	CCO:MP0001785
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000608	dissociated hepatocytes	CCO:MP0000608
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000783	abnormal forebrain morphology	CCO:MP0000783
MGI:96646	Jun	Jun<tm1Bdc>/Jun<tm1Bdc>	Not Specified	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6)	MP:0000255	vasculature congestion	CCO:MP0000255
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:96646	Jun	Jun<tm2.1Wag>/Jun<tm2.1Wag>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0008236	decreased susceptibility to neuronal excitotoxicity	CCO:MP0008236
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0003887	increased hepatocyte apoptosis	CCO:MP0003887
MGI:96646	Jun	Jun<tm2.1Wag>/Jun<tm2.1Wag>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001262	decreased body weight	CCO:MP0001262
MGI:96646	Jun	Jun<tm2.1Wag>/Jun<tm2.1Wag>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:96646	Jun	Jun<tm2.1Wag>/Jun<tm2.1Wag>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001265	decreased body size	CCO:MP0001265
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0001575	cyanosis	CCO:MP0001575
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:96646	Jun	Jun<tm2.1Wag>/Jun<tm2.1Wag>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002887	increased resistance to pharmacologically induced seizures	CCO:MP0002887
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:96646	Jun	Jun<tm2.1Wag>/Jun<tm2.1Wag>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0004001	decreased hepatocyte proliferation	CCO:MP0004001
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002977	abnormal patterning of the aortic arch	CCO:MP0002977
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002950	abnormal neural crest cell migration	CCO:MP0002950
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002658	abnormal liver regeneration	CCO:MP0002658
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Alb1-cre)7Gsc/0"	involves: 129P2/OlaHsd * FVB/N	MP:0003402	decreased liver weight	CCO:MP0003402
MGI:96646	Jun	Jun<tm1Pa>/Jun<tm1Pa>	either: (involves: 129S/SvEv * 129X1/SvJ) or (involves: 129X1/SvJ * C57BL/6J)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:96646	Jun	Jun<tm1Pa>/Jun<tm1Pa>	either: (involves: 129S/SvEv * 129X1/SvJ) or (involves: 129X1/SvJ * C57BL/6J)	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Alb1-cre)7Gsc/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002658	abnormal liver regeneration	CCO:MP0002658
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Alb1-cre)7Gsc/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001265	decreased body size	CCO:MP0001265
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(COL2A1-cre)1Wag/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004624	abnormal thoracic cage	CCO:MP0004624
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0009264	failure of eyelid fusion	CCO:MP0009264
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004613	fusion of vertebral arches	CCO:MP0004613
MGI:96646	Jun	Jun<tm3.1Wag>/Jun<tm3.1Wag>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000161	scoliosis	CCO:MP0000161
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000160	kyphosis	CCO:MP0000160
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001258	decreased body length	CCO:MP0001258
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001265	decreased body size	CCO:MP0001265
MGI:96646	Jun	Jun<tm1Wag>/Jun<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:96646	Jun	"Jun<tm4Wag>/Jun<tm4Wag>,Tg(COL2A1-cre)1Wag/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000161	scoliosis	CCO:MP0000161
MGI:96646	Jun	Jun<tm1(Junb)Wag>/Jun<tm1(Junb)Wag>	involves: 129P2/OlaHsd * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:96646	Jun	"Jun<tm1Rsjo>/Jun<tm1Rsjo>,Tg(KRT14-cre)8Brn/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0001792	impaired wound healing	CCO:MP0001792
MGI:96646	Jun	"Jun<tm1Rsjo>/Jun<tm1Rsjo>,Tg(KRT14-cre)8Brn/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0001313	increased incidence of corneal inflammation	CCO:MP0001313
MGI:96646	Jun	"Jun<tm1Rsjo>/Jun<tm1Rsjo>,Tg(KRT14-cre)8Brn/0"	involves: 129S1/Sv * 129X1/SvJ	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:96646	Jun	"Jun<tm1Wag>/Jun<tm1Wag>,Tg(Junb)1598Angl/0"	involves: 129S2/SvPas * C57BL/6	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:96646	Jun	"Jun<tm1Wag>/Jun<tm1Wag>,Tg(Junb)1598Angl/0"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:96646	Jun	"Jun<tm1Wag>/Jun<tm1Wag>,Tg(Junb)1598Angl/0"	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:96646	Jun	"Jun<tm1Wag>/Jun<tm1Wag>,Tg(Junb)1598Angl/0"	involves: 129S2/SvPas * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:96646	Jun	"Jun<tm1Wag>/Jun<tm1Wag>,Tg(Junb)1598Angl/0"	involves: 129S2/SvPas * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:96647	Junb	Junb<tm1Wag>/Junb<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96647	Junb	Junb<tm2Wag>/Junb<tm2Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002088	abnormal embryonic growth/weight/body size	CCO:MP0002088
MGI:96647	Junb	Junb<tm2Wag>/Junb<tm2Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:96647	Junb	Junb<tm1Wag>/Junb<+>	involves: 129S2/SvPas * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96647	Junb	Junb<tm1Wag>/Junb<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002088	abnormal embryonic growth/weight/body size	CCO:MP0002088
MGI:96647	Junb	Junb<tm2Wag>/Junb<tm2Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96647	Junb	Junb<tm1Wag>/Junb<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:96647	Junb	Junb<tm1Wag>/Junb<tm1Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:96647	Junb	Junb<tm2Wag>/Junb<tm2Wag>	involves: 129S2/SvPas * C57BL/6	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0000135	decreased cortical bone thickness	CCO:MP0000135
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0000063	decreased bone density	CCO:MP0000063
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Lyz2<tm1(cre)Ifo>/Lyz2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0000057	abnormal osteogenesis	CCO:MP0000057
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Lyz2<tm1(cre)Ifo>/Lyz2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0004982	abnormal osteoclast morphology	CCO:MP0004982
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0000057	abnormal osteogenesis	CCO:MP0000057
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0004993	decreased bone resorption	CCO:MP0004993
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0005481	chronic myelocytic leukemia	CCO:MP0005481
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0004991	decreased bone strength	CCO:MP0004991
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0001533	abnormal skeleton physiology	CCO:MP0001533
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0004985	decreased osteoclast cell number	CCO:MP0004985
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002113	abnormal skeleton development	CCO:MP0002113
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002764	short tibia	CCO:MP0002764
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Lyz2<tm1(cre)Ifo>/Lyz2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0000130	abnormal cancellous bone morphology	CCO:MP0000130
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0008396	abnormal osteoclast differentiation	CCO:MP0008396
MGI:96647	Junb	"Junb<tm3Wag>/Junb<tm3Wag>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129P2/OlaHsd * C57BL/6	MP:0004989	decreased osteoblast cell number	CCO:MP0004989
MGI:1343094	Kat2b	"Kat2a<tm1Nkt>/Kat2a<tm1Nkt>,Kat2b<tm1Nkt>/Kat2b<tm1Nkt>"	involves: CD-1	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1343094	Kat2b	Kat2b<tm1Nkt>/Kat2b<tm1Nkt>	involves: CD-1	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1343094	Kat2b	"Kat2a<tm1Nkt>/Kat2a<tm1Nkt>,Kat2b<tm1Nkt>/Kat2b<tm1Nkt>"	involves: CD-1	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1343094	Kat2b	Kat2b<tm1Roth>/Kat2b<tm1Roth>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1343094	Kat2b	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Kat2b<tm1Roth>/Kat2b<tm1Roth>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1343094	Kat2b	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Kat2b<tm1Roth>/Kat2b<tm1Roth>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1343094	Kat2b	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Kat2b<tm1Roth>/Kat2b<tm1Roth>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:1343094	Kat2b	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Kat2b<tm1Roth>/Kat2b<tm1Roth>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0005006	abnormal osteoblast physiology	CCO:MP0005006
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0001533	abnormal skeleton physiology	CCO:MP0001533
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0000168	abnormal bone marrow development	CCO:MP0000168
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0000062	increased bone density	CCO:MP0000062
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0002998	abnormal bone remodeling	CCO:MP0002998
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0005666	abnormal adipose tissue physiology	CCO:MP0005666
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0005668	decreased circulating leptin level	CCO:MP0005668
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0001386	abnormal maternal nurturing	CCO:MP0001386
MGI:893579	Khdrbs1	Khdrbs1<tm1Rchd>/Khdrbs1<tm1Rchd>	involves: C57BL/6	MP:0005605	increased bone mass	CCO:MP0005605
MGI:1098231	Kif11	Kif11<Gt(XE579)Byg>/Kif11<Gt(XE579)Byg>	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1098231	Kif11	Kif11<Gt(XE579)Byg>/Kif11<Gt(XE579)Byg>	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1098231	Kif11	Kif11<Gt(XE579)Byg>/Kif11<Gt(XE579)Byg>	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1098231	Kif11	Kif11<tm1Much>/Kif11<tm1Much>	involves: 129S2/SvPas * C57BL/6	MP:0001728	failure of embryo implantation	CCO:MP0001728
MGI:1098231	Kif11	Kif11<tm1Much>/Kif11<tm1Much>	involves: 129S2/SvPas * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1098231	Kif11	Kif11<tm1Much>/Kif11<tm1Much>	involves: 129S2/SvPas * C57BL/6	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:1098231	Kif11	Kif11<tm1Much>/Kif11<tm1Much>	involves: 129S2/SvPas * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0002773	decreased circulating luteinizing hormone level	CCO:MP0002773
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0009009	absent estrous cycle	CCO:MP0009009
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0008366	enlarged adenohypophysis	CCO:MP0008366
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0005120	decreased circulating growth hormone level	CCO:MP0005120
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0002682	decreased mature ovarian follicle number	CCO:MP0002682
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0005121	decreased circulating prolactin level	CCO:MP0005121
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0001921	reduced fertility	CCO:MP0001921
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0001129	impaired ovarian folliculogenesis	CCO:MP0001129
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0001634	internal hemorrhage	CCO:MP0001634
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0001926	female infertility	CCO:MP0001926
MGI:1333883	Lats1	Lats1<tm1Tx>/Lats1<tm1Tx>	involves: 129S2/SvPas * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0004025	polyploidy	CCO:MP0004025
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0003707	increased nucleus count	CCO:MP0003707
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0002884	abnormal branchial arch morphology	CCO:MP0002884
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<+>	involves: 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0000828	abnormal fourth ventricle morphology	CCO:MP0000828
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0002188	small heart	CCO:MP0002188
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0000736	delayed muscle development	CCO:MP0000736
MGI:1354386	Lats2	Lats2<tm1Noj>/Lats2<tm1Noj>	involves: 129S2/SvPas * C57BL/6	MP:0000955	abnormal spinal cord morphology	CCO:MP0000955
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0003105	abnormal heart atrium morphology	CCO:MP0003105
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1354386	Lats2	Lats2<tm1Dgen>/Lats2<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0005244	hemopericardium	CCO:MP0005244
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0000930	wavy neural tube	CCO:MP0000930
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0000295	poorly developed ventricular trabeculae	CCO:MP0000295
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0000279	ventricular hypoplasia	CCO:MP0000279
MGI:1354386	Lats2	Lats2<tm1Raz>/Lats2<tm1Raz>	involves: 129P2/OlaHsd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1354386	Lats2	Lats2<tm1Dgen>/Lats2<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0001486	abnormal startle reflex	CCO:MP0001486
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Ripply2<tm1.1Ysa>/Ripply2<tm1.1Ysa>"	involves: 129S7/SvEvBrd * C57BL/6 * CBA * ICR	MP:0000140	absent vertebral pedicles	CCO:MP0000140
MGI:1095413	Lfng	"Jag2<tm1Grid>/Jag2<tm1Grid>,Lfng<tm1Grid>/Lfng<+>"	involves: 129S1/Sv * C57BL/6J	MP:0004396	decreased cochlear inner hair cell number	CCO:MP0004396
MGI:1095413	Lfng	"Jag2<tm1Grid>/Jag2<tm1Grid>,Lfng<tm1Grid>/Lfng<tm1Grid>"	involves: 129S1/Sv * C57BL/6J	MP:0004401	increased cochlear outer hair cell number	CCO:MP0004401
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Ripply2<tm1.1Ysa>/Ripply2<tm1.1Ysa>"	involves: 129S7/SvEvBrd * C57BL/6 * CBA * ICR	MP:0005221	abnormal rostral-caudal axis patterning	CCO:MP0005221
MGI:1095413	Lfng	"Jag2<tm1Grid>/Jag2<tm1Grid>,Lfng<tm1Grid>/Lfng<tm1Grid>"	involves: 129S1/Sv * C57BL/6J	MP:0004399	abnormal cochlear outer hair cell morphology	CCO:MP0004399
MGI:1095413	Lfng	"Jag2<tm1Grid>/Jag2<tm1Grid>,Lfng<tm1Grid>/Lfng<tm1Grid>"	involves: 129S1/Sv * C57BL/6J	MP:0004396	decreased cochlear inner hair cell number	CCO:MP0004396
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6 * CBA * ICR	MP:0005221	abnormal rostral-caudal axis patterning	CCO:MP0005221
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	MP:0000592	short tail	CCO:MP0000592
MGI:1095413	Lfng	Lfng<m1Btlr>/Lfng<m1Btlr>	C57BL/6J-Lfng<m1Btlr>	MP:0000592	short tail	CCO:MP0000592
MGI:1095413	Lfng	Lfng<m1Btlr>/Lfng<m1Btlr>	C57BL/6J-Lfng<m1Btlr>	MP:0000585	kinked tail	CCO:MP0000585
MGI:1095413	Lfng	Lfng<m1Btlr>/Lfng<m1Btlr>	C57BL/6J-Lfng<m1Btlr>	MP:0001921	reduced fertility	CCO:MP0001921
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	MP:0008530	abnormal rostral-caudal patterning of the somites	CCO:MP0008530
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	MP:0003047	abnormal thoracic vertebrae morphology	CCO:MP0003047
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	MP:0003050	abnormal sacral vertebrae morphology	CCO:MP0003050
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	MP:0003049	abnormal lumbar vertebrae morphology	CCO:MP0003049
MGI:1095413	Lfng	Lfng<m1Btlr>/Lfng<m1Btlr>	C57BL/6J-Lfng<m1Btlr>	MP:0004609	vertebral fusion	CCO:MP0004609
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	MP:0001925	male infertility	CCO:MP0001925
MGI:1095413	Lfng	Lfng<tm1Seco>/Lfng<tm1Seco>	involves: 129S6/SvEvTac * C57BL/6J	MP:0003047	abnormal thoracic vertebrae morphology	CCO:MP0003047
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1095413	Lfng	Lfng<tm1Seco>/Lfng<tm1Seco>	involves: 129S6/SvEvTac * C57BL/6J	MP:0008530	abnormal rostral-caudal patterning of the somites	CCO:MP0008530
MGI:1095413	Lfng	Lfng<tm1Seco>/Lfng<tm1Seco>	involves: 129S6/SvEvTac * C57BL/6J	MP:0003049	abnormal lumbar vertebrae morphology	CCO:MP0003049
MGI:1095413	Lfng	Lfng<tm1Seco>/Lfng<tm1Seco>	involves: 129S6/SvEvTac * C57BL/6J	MP:0000154	rib fusion	CCO:MP0000154
MGI:1095413	Lfng	Lfng<tm1Seco>/Lfng<tm1Seco>	involves: 129S6/SvEvTac * C57BL/6J	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:1095413	Lfng	Lfng<tm1Seco>/Lfng<tm1Seco>	involves: 129S6/SvEvTac * C57BL/6J	MP:0001258	decreased body length	CCO:MP0001258
MGI:1095413	Lfng	Lfng<tm1Seco>/Lfng<tm1Seco>	involves: 129S6/SvEvTac * C57BL/6J	MP:0000585	kinked tail	CCO:MP0000585
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)	MP:0000154	rib fusion	CCO:MP0000154
MGI:1095413	Lfng	Lfng<tm1Seco>/Lfng<tm1Seco>	involves: 129S6/SvEvTac * C57BL/6J	MP:0005222	abnormal somite size	CCO:MP0005222
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>,Rfng<tm1Tfv>/Rfng<tm1Tfv>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0001539	decreased caudal vertebrae number	CCO:MP0001539
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>,Rfng<tm1Tfv>/Rfng<tm1Tfv>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>,Rfng<tm1Tfv>/Rfng<tm1Tfv>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0001539	decreased caudal vertebrae number	CCO:MP0001539
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>,Rfng<tm1Tfv>/Rfng<tm1Tfv>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0005508	abnormal skeleton morphology	CCO:MP0005508
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0001539	decreased caudal vertebrae number	CCO:MP0001539
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:1095413	Lfng	"Lfng<tm1Rjo>/Lfng<tm1Rjo>,Mfng<tm1Seco>/Mfng<tm1Seco>,Rfng<tm1Tfv>/Rfng<tm1Tfv>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J * FVB/NJ	MP:0005508	abnormal skeleton morphology	CCO:MP0005508
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001129	impaired ovarian folliculogenesis	CCO:MP0001129
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1095413	Lfng	"Lfng<tm1Grid>/Lfng<tm1Grid>,Rfng<tm1Grid>/Rfng<tm1Grid>"	involves: 129S1/SvImJ * C57BL/6J	MP:0008149	abnormal rib-vertebral column attachment	CCO:MP0008149
MGI:1095413	Lfng	"Lfng<tm1Grid>/Lfng<tm1Grid>,Rfng<tm1Grid>/Rfng<tm1Grid>"	involves: 129S1/SvImJ * C57BL/6J	MP:0000153	rib bifurcation	CCO:MP0000153
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008530	abnormal rostral-caudal patterning of the somites	CCO:MP0008530
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004609	vertebral fusion	CCO:MP0004609
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005227	abnormal vertebral body development	CCO:MP0005227
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000154	rib fusion	CCO:MP0000154
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001125	abnormal oocyte morphology	CCO:MP0001125
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001127	small ovary	CCO:MP0001127
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005225	abnormal vertebrae development	CCO:MP0005225
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0004624	abnormal thoracic cage	CCO:MP0004624
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0001926	female infertility	CCO:MP0001926
MGI:1095413	Lfng	Lfng<tm1Rjo>/Lfng<tm1Rjo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0000154	rib fusion	CCO:MP0000154
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0000153	rib bifurcation	CCO:MP0000153
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0000963	fused dorsal root ganglion	CCO:MP0000963
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0005223	abnormal anterior-posterior polarity of the somites	CCO:MP0005223
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0003345	decreased rib number	CCO:MP0003345
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0004646	decreased cervical vertebrae number	CCO:MP0004646
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0008148	abnormal rib-sternum attachment	CCO:MP0008148
MGI:1095413	Lfng	Lfng<tm1Grid>/Lfng<tm1Grid>	involves: 129S1/SvImJ	MP:0008149	abnormal rib-vertebral column attachment	CCO:MP0008149
MGI:1095413	Lfng	"Lfng<tm1Grid>/Lfng<tm1Grid>,Rfng<tm1Grid>/Rfng<tm1Grid>"	involves: 129S1/SvImJ * C57BL/6J	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:1095413	Lfng	"Lfng<tm1Grid>/Lfng<tm1Grid>,Rfng<tm1Grid>/Rfng<tm1Grid>"	involves: 129S1/SvImJ * C57BL/6J	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:1095413	Lfng	"Lfng<tm1Grid>/Lfng<tm1Grid>,Rfng<tm1Grid>/Rfng<tm1Grid>"	involves: 129S1/SvImJ * C57BL/6J	MP:0000154	rib fusion	CCO:MP0000154
MGI:96787	Lif	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6J	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:96787	Lif	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6J	MP:0001120	abnormal uterus morphology	CCO:MP0001120
MGI:96787	Lif	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6J	MP:0001728	failure of embryo implantation	CCO:MP0001728
MGI:96787	Lif	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:96787	Lif	Lif<tm1Phb>/Lif<tm1Phb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:96787	Lif	Lif<tm1Stw>/Lif<tm1Stw>	involves: 129S1/Sv * C57BL/6J	MP:0001926	female infertility	CCO:MP0001926
MGI:96787	Lif	Lif<tm1Phb>/Lif<tm1Phb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:96787	Lif	Lif<tm1Cgre>/Lif<tm1Cgre>	involves: MF1	MP:0005011	increased eosinophil cell number	CCO:MP0005011
MGI:96787	Lif	Lif<tm1Cgre>/Lif<tm1Cgre>	involves: MF1	MP:0002446	abnormal macrophage morphology	CCO:MP0002446
MGI:96787	Lif	Lif<tm1Cgre>/Lif<tm1Cgre>	involves: MF1	MP:0001120	abnormal uterus morphology	CCO:MP0001120
MGI:96787	Lif	Lif<tm1Cgre>/Lif<tm1Cgre>	involves: MF1	MP:0009394	increased uterine NK cell number	CCO:MP0009394
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0008973	decreased erythroid progenitor cell number	CCO:MP0008973
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0000248	macrocytosis	CCO:MP0000248
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0009308	adenocarcinoma	CCO:MP0009308
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0009278	abnormal bone marrow cell physiology	CCO:MP0009278
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0003717	pallor	CCO:MP0003717
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0002643	poikilocytosis	CCO:MP0002643
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0002642	anisocytosis	CCO:MP0002642
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0000215	absent erythrocytes	CCO:MP0000215
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0001577	anemia	CCO:MP0001577
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0001577	anemia	CCO:MP0001577
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0002429	abnormal blood cell morphology/development	CCO:MP0002429
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0000601	small liver	CCO:MP0000601
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0000596	abnormal liver development	CCO:MP0000596
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:101789	Lig1	Lig1<tm2Dwm>/Lig1<tm2Dwm>	involves: 129P2/OlaHsd	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0002640	reticulocytosis	CCO:MP0002640
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0008057	abnormal DNA replication	CCO:MP0008057
MGI:101789	Lig1	Lig1<tm2Dwm>/Lig1<tm2Dwm>	involves: 129P2/OlaHsd	MP:0001577	anemia	CCO:MP0001577
MGI:101789	Lig1	Lig1<tm2Dwm>/Lig1<tm2Dwm>	involves: 129P2/OlaHsd	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd * BALB/c	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0002640	reticulocytosis	CCO:MP0002640
MGI:101789	Lig1	Lig1<tm1Dwm>/Lig1<tm1Dwm>	involves: 129P2/OlaHsd	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0003763	abnormal thymus physiology	CCO:MP0003763
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0008737	abnormal spleen physiology	CCO:MP0008737
MGI:101789	Lig1	Lig1<tm3Dwm>/Lig1<tm3Dwm>	involves: 129P2/OlaHsd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:109152	Lig3	Lig3<tm1Czhu>/Lig3<tm1Czhu>	involves: 129/Sv	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:109152	Lig3	Lig3<tm1Czhu>/Lig3<tm1Czhu>	involves: 129/Sv	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:109152	Lig3	Lig3<tm1Czhu>/Lig3<tm1Czhu>	involves: 129/Sv	MP:0003701	elevated level of sister chromatid exchange	CCO:MP0003701
MGI:109152	Lig3	Lig3<tm1Czhu>/Lig3<tm1Czhu>	involves: 129/Sv	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:109152	Lig3	Lig3<tm1Czhu>/Lig3<tm1Czhu>	involves: 129/Sv	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1335098	Lig4	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:1335098	Lig4	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1335098	Lig4	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0005014	increased B cell number	CCO:MP0005014
MGI:1335098	Lig4	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1335098	Lig4	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1335098	Lig4	"Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129S6/SvEvTac * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1335098	Lig4	"Cdkn2a<tm1Rdp>/Cdkn2a<+>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1335098	Lig4	"Xrcc5<tm1Dbr>/Xrcc5<+>,Lig4<tm1Fwa>/Lig4<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002022	lymphoma	CCO:MP0002022
MGI:1335098	Lig4	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<+>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0000727	absent CD8-positive T cells	CCO:MP0000727
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<+>	involves: 129S6/SvEvTac * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:1335098	Lig4	"Atm<tm1Pmc>/Atm<+>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0002416	abnormal proerythroblast morphology	CCO:MP0002416
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:1335098	Lig4	Lig4<tm1Icrf>/Lig4<tm1Icrf>	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1335098	Lig4	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0001265	decreased body size	CCO:MP0001265
MGI:1335098	Lig4	"Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002619	abnormal lymphocyte morphology	CCO:MP0002619
MGI:1335098	Lig4	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1335098	Lig4	"Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1335098	Lig4	Lig4<tm1Icrf>/Lig4<tm1Icrf>	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1335098	Lig4	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<+>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<+>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0002083	premature death	CCO:MP0002083
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<+>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:1335098	Lig4	Lig4<tiny>/Lig4<tiny>	C57BL/6JApb-Lig4<tiny>/Apb	MP:0001265	decreased body size	CCO:MP0001265
MGI:1335098	Lig4	"Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>,Lig4<tm1Fwa>/Lig4<tm1Fwa>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:1335098	Lig4	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ)	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1335098	Lig4	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	involves: 129	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1335098	Lig4	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Icrf>/Lig4<tm1Icrf>"	involves: 129	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Nbn<tm1Jpt>/Nbn<tm1Jpt>"	involves: 129 * 129S7/SvEvBrd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Nbn<tm1Jpt>/Nbn<tm1Jpt>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0000433	microcephaly	CCO:MP0000433
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Nbn<tm1Jpt>/Nbn<tm1Jpt>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0000913	abnormal brain development	CCO:MP0000913
MGI:1335098	Lig4	"Atm<tm1Pmc>/Atm<tm1Pmc>,Lig4<tm1Pmc>/Lig4<tm1Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * C57BL/6 * SJL	MP:0001393	ataxia	CCO:MP0001393
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Nbn<tm1Jpt>/Nbn<tm1Jpt>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<+>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<+>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<+>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Meox2<tm1(cre)Sor>/Meox2<+>"	involves: 129S1/Sv	MP:0003861	abnormal nervous system development	CCO:MP0003861
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * C57BL/6 * SJL	MP:0000774	decreased brain size	CCO:MP0000774
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>"	involves: 129 * 129/Sv	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * C57BL/6 * SJL	MP:0000433	microcephaly	CCO:MP0000433
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * C57BL/6 * SJL	MP:0000913	abnormal brain development	CCO:MP0000913
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * C57BL/6 * SJL	MP:0001393	ataxia	CCO:MP0001393
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * C57BL/6 * SJL	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Mre11a<tm1Jpt>/Mre11a<tm1Jpt>"	involves: 129 * 129S7/SvEvBrd	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1335098	Lig4	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Mre11a<tm1Jpt>/Mre11a<tm1Jpt>"	involves: 129 * 129S7/SvEvBrd	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0001393	ataxia	CCO:MP0001393
MGI:1335098	Lig4	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * C57BL/6 * SJL	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac	MP:0004030	induced chromosome breakage	CCO:MP0004030
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0002144	abnormal B cell differentiation	CCO:MP0002144
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0000706	small thymus	CCO:MP0000706
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0001825	arrested T cell differentiation	CCO:MP0001825
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:1335098	Lig4	Lig4<tm1Icrf>/Lig4<tm1Icrf>	involves: 129	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1335098	Lig4	Lig4<tm1Icrf>/Lig4<tm1Icrf>	involves: 129	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0001802	arrested B cell differentiation	CCO:MP0001802
MGI:1335098	Lig4	Lig4<tm1Fwa>/Lig4<tm1Fwa>	involves: 129S6/SvEvTac * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1919818	Lin9	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1919818	Lin9	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0001926	female infertility	CCO:MP0001926
MGI:1919818	Lin9	Lin9<tm1Orc>/Lin9<tm1Orc>	Not Specified	MP:0001260	increased body weight	CCO:MP0001260
MGI:1919818	Lin9	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1919818	Lin9	"Cdk4<tm1Kiyo>/Cdk4<+>,Lin9<tm1Orc>/Lin9<+>"	involves: 129S1/Sv	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1919818	Lin9	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0008365	adenohypophysis hypoplasia	CCO:MP0008365
MGI:1919818	Lin9	"Cdk4<tm1Kiyo>/Cdk4<tm1Kiyo>,Lin9<tm1Orc>/Lin9<tm1Orc>"	involves: 129S1/Sv	MP:0001925	male infertility	CCO:MP0001925
MGI:1919818	Lin9	"Cdk4<tm1Kiyo>/Cdk4<+>,Lin9<tm1Orc>/Lin9<+>"	involves: 129S1/Sv	MP:0004804	decreased susceptibility to autoimmune diabetes	CCO:MP0004804
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0006079	stomach tumor	CCO:MP0006079
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<+>	involves: 129/Sv * C57BL/6J	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<+>	involves: 129/Sv * C57BL/6J	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<+>	involves: 129/Sv * C57BL/6J	MP:0008010	gastric adenocarcinoma	CCO:MP0008010
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<+>	involves: 129/Sv * C57BL/6J	MP:0006079	stomach tumor	CCO:MP0006079
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<+>	involves: 129/Sv * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<+>	involves: 129/Sv * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<+>	involves: 129/Sv * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<+>	involves: 129/Sv * C57BL/6J	MP:0002048	lung adenoma	CCO:MP0002048
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0008010	gastric adenocarcinoma	CCO:MP0008010
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:2684762	Lzts1	Lzts1<tm1Cro>/Lzts1<tm1Cro>	involves: 129/Sv * C57BL/6J	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:108559	Macf1	Macf1<tm1Liem>/Macf1<tm1Liem>	involves: 129S6/SvEvTac * C57BL/6J	MP:0001683	absent mesoderm	CCO:MP0001683
MGI:108559	Macf1	Macf1<tm1Liem>/Macf1<tm1Liem>	involves: 129S6/SvEvTac * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:108559	Macf1	Macf1<tm1Liem>/Macf1<tm1Liem>	involves: 129S6/SvEvTac * C57BL/6J	MP:0001693	failure of primitive streak formation	CCO:MP0001693
MGI:108559	Macf1	"Macf1<tm1Efu>/Macf1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	Not Specified	MP:0002908	delayed wound healing	CCO:MP0002908
MGI:108559	Macf1	"Macf1<tm1Efu>/Macf1<tm1Efu>,Tg(KRT14-cre)1Efu/0"	Not Specified	MP:0003453	abnormal keratinocyte physiology	CCO:MP0003453
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<tm1.1Ktj>	involves: BALB/c * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1341857	Mad1l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1341857	Mad1l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1341857	Mad1l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:1341857	Mad1l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1341857	Mad1l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:1341857	Mad1l1	Mad1l1<tm1.1Ktj>/Mad1l1<+>	involves: BALB/c * C57BL/6J	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:1860374	Mad2l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<+>	involves: 129S2/SvPas	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:1860374	Mad2l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<+>	involves: 129S2/SvPas	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<+>	involves: 129S2/SvPas	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1860374	Mad2l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1860374	Mad2l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<+>	involves: 129S2/SvPas	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1860374	Mad2l1	"Mad1l1<tm1.1Ktj>/Mad1l1<+>,Mad2l1<tm1Sorg>/Mad2l1<+>"	involves: 129S2/SvPas * BALB/c * C57BL/6J	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<tm1Sorg>	involves: 129S2/SvPas * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<tm1Sorg>	involves: 129S2/SvPas * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<tm1Sorg>	involves: 129S2/SvPas * C57BL/6	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<tm1Sorg>	involves: 129S2/SvPas * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<tm1Sorg>	involves: 129S2/SvPas * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<tm1Sorg>	involves: 129S2/SvPas * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<tm1Sorg>	involves: 129S2/SvPas * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<+>	involves: 129S2/SvPas * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<+>	involves: 129S2/SvPas * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<+>	involves: 129S2/SvPas * C57BL/6	MP:0008481	increased spleen germinal center number	CCO:MP0008481
MGI:1860374	Mad2l1	Mad2l1<tm1Sorg>/Mad2l1<tm1Sorg>	involves: 129S2/SvPas * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ * C57BL/6 * DBA/2	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ * C57BL/6 * DBA/2	MP:0004792	abnormal synaptic vesicle number	CCO:MP0004792
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ * C57BL/6 * DBA/2	MP:0001053	abnormal neuromuscular synapse morphology	CCO:MP0001053
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ * C57BL/6 * DBA/2	MP:0001953	respiratory failure	CCO:MP0001953
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ * C57BL/6 * DBA/2	MP:0002578	impaired ability to fire action potentials	CCO:MP0002578
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ * C57BL/6 * DBA/2	MP:0005498	hyporesponsive to tactile stimuli	CCO:MP0005498
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ * C57BL/6 * DBA/2	MP:0004769	abnormal synaptic vesicle morphology	CCO:MP0004769
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ	MP:0004769	abnormal synaptic vesicle morphology	CCO:MP0004769
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ	MP:0004753	abnormal miniature excitatory postsynaptic currents	CCO:MP0004753
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ	MP:0002910	abnormal excitatory postsynaptic currents	CCO:MP0002910
MGI:2444672	Madd	Madd<tm1Ytk>/Madd<tm1Ytk>	involves: 129X1/SvJ * C57BL/6 * DBA/2	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1891748	Maea	Maea<Gt(XG702)Byg>/Maea<Gt(XG702)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:1891748	Maea	Maea<Gt(XG702)Byg>/Maea<Gt(XG702)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:1891748	Maea	Maea<Gt(XG702)Byg>/Maea<Gt(XG702)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003717	pallor	CCO:MP0003717
MGI:1891748	Maea	Maea<Gt(XG702)Byg>/Maea<Gt(XG702)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1891748	Maea	Maea<Gt(XG702)Byg>/Maea<Gt(XG702)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:1891748	Maea	Maea<Gt(XG702)Byg>/Maea<Gt(XG702)Byg>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:2138453	Mael	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	MP:0001925	male infertility	CCO:MP0001925
MGI:2138453	Mael	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:2138453	Mael	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:2138453	Mael	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:2138453	Mael	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	MP:0008878	abnormal DNA methylation during gametogenesis	CCO:MP0008878
MGI:2138453	Mael	"Mael<tm1Bort>/Mael<tm1Bort>,Spo11<tm1Rdco>/Spo11<tm1Rdco>"	involves: 129 * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:2138453	Mael	Mael<tm1Bort>/Mael<tm1Bort>	B6.129S4-Mael<tm1Bort>	MP:0001147	small testis	CCO:MP0001147
MGI:1346878	Map3k8	"Map3k8<tm1Ceci>/Map3k8<tm1Ceci>,Tnf<tm2Gkl>/Tnf<+>"	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	MP:0008082	increased single-positive T cell number	CCO:MP0008082
MGI:1346878	Map3k8	"Map3k8<tm1Ceci>/Map3k8<tm1Ceci>,Tnf<tm2Gkl>/Tnf<+>"	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	MP:0008078	increased CD8-positive T cell number	CCO:MP0008078
MGI:1346878	Map3k8	"Map3k8<tm1Ceci>/Map3k8<tm1Ceci>,Tnf<tm2Gkl>/Tnf<+>"	involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J	MP:0003306	small intestinal inflammation	CCO:MP0003306
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0008706	decreased interleukin-6 secretion	CCO:MP0008706
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<+>	C57BL/6J-Map3k8<m1Btlr>	MP:0008556	abnormal tumor necrosis factor secretion	CCO:MP0008556
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0008563	decreased interferon-alpha secretion	CCO:MP0008563
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<+>	C57BL/6J-Map3k8<m1Btlr>	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<+>	C57BL/6J-Map3k8<m1Btlr>	MP:0008561	decreased tumor necrosis factor secretion	CCO:MP0008561
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0005025	abnormal response to infection	CCO:MP0005025
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0008561	decreased tumor necrosis factor secretion	CCO:MP0008561
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0008565	decreased interferon-beta secretion	CCO:MP0008565
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0008658	decreased interleukin-1 beta secretion	CCO:MP0008658
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0008669	increased interleukin-12b secretion	CCO:MP0008669
MGI:1346878	Map3k8	Map3k8<m1Btlr>/Map3k8<m1Btlr>	C57BL/6J-Map3k8<m1Btlr>	MP:0005070	impaired NK cell cytolysis	CCO:MP0005070
MGI:1346878	Map3k8	Map3k8<tm1Ceci>/Map3k8<tm1Ceci>	involves: 129S1/Sv * C57BL/6J	MP:0008734	decreased susceptibility to endotoxin shock	CCO:MP0008734
MGI:1346878	Map3k8	Map3k8<tm1Ceci>/Map3k8<tm1Ceci>	involves: 129S1/Sv * C57BL/6J	MP:0008561	decreased tumor necrosis factor secretion	CCO:MP0008561
MGI:1346878	Map3k8	Map3k8<tm1Tmat>/Map3k8<tm1Tmat>	involves: 129S/SvEv * C57BL/6	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:1346878	Map3k8	Map3k8<tm1Tmat>/Map3k8<tm1Tmat>	involves: 129S/SvEv * C57BL/6	MP:0008495	decreased IgG1 level	CCO:MP0008495
MGI:1346878	Map3k8	Map3k8<tm1Tmat>/Map3k8<tm1Tmat>	involves: 129S/SvEv * C57BL/6	MP:0008500	increased IgG2a level	CCO:MP0008500
MGI:1346878	Map3k8	Map3k8<tm1Tmat>/Map3k8<tm1Tmat>	involves: 129S/SvEv * C57BL/6	MP:0002455	abnormal dendritic cell antigen presentation	CCO:MP0002455
MGI:1346878	Map3k8	Map3k8<tm1Tmat>/Map3k8<tm1Tmat>	involves: 129S/SvEv * C57BL/6	MP:0003009	abnormal cytokine secretion	CCO:MP0003009
MGI:1346878	Map3k8	Map3k8<tm1Tmat>/Map3k8<tm1Tmat>	involves: 129S/SvEv * C57BL/6	MP:0002492	decreased IgE level	CCO:MP0002492
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0005094	abnormal T cell proliferation	CCO:MP0005094
MGI:1346858	Mapk1	Mapk1<tm2Hed>/Mapk1<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004179	transmission ratio distortion	CCO:MP0004179
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0000706	small thymus	CCO:MP0000706
MGI:1346858	Mapk1	Mapk1<tm2Hed>/Mapk1<tm2Hed>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(CD4-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0003944	abnormal T cell subpopulation ratio	CCO:MP0003944
MGI:1346858	Mapk1	"Mapk1<tm1.1Hed>/Mapk1<tm1.1Hed>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0005319	abnormal enzyme/ coenzyme level	CCO:MP0005319
MGI:1346858	Mapk1	"Mapk1<tm1.1Hed>/Mapk1<tm1.1Hed>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0003944	abnormal T cell subpopulation ratio	CCO:MP0003944
MGI:1346858	Mapk1	"Mapk1<tm1.1Hed>/Mapk1<tm1.1Hed>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CD4-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0004919	abnormal positive T cell selection	CCO:MP0004919
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(TcrAND)53Hed/0"	involves: C57BL/6 * DBA/2 * SJL	MP:0004919	abnormal positive T cell selection	CCO:MP0004919
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CD4-cre)1Cwi/0,Tg(TcrAND)53Hed/0"	involves: C57BL/6 * DBA/2 * SJL	MP:0004919	abnormal positive T cell selection	CCO:MP0004919
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CD4-cre)1Cwi/0,Tg(TcrAND)53Hed/0"	involves: C57BL/6 * DBA/2 * SJL	MP:0003944	abnormal T cell subpopulation ratio	CCO:MP0003944
MGI:1346858	Mapk1	"Mapk1<tm1.1Hed>/Mapk1<tm1.1Hed>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(Lck-cre)1Cwi/0,Tg(TcrAND)53Hed/0"	involves: C57BL/6 * DBA/2 * SJL	MP:0004919	abnormal positive T cell selection	CCO:MP0004919
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(TcraTcrb)1100Mjb/0"	involves: C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(TcraTcrb)1100Mjb/0"	involves: C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(CD4-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0004919	abnormal positive T cell selection	CCO:MP0004919
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(TcrAND)53Hed/0"	involves: C57BL/6 * DBA/2 * SJL	MP:0002408	abnormal double-positive T cell morphology	CCO:MP0002408
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0005091	increased double-positive T cell number	CCO:MP0005091
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(Lck-cre)1Cwi/0,Tg(TcrAND)53Hed/0"	involves: C57BL/6 * DBA/2 * SJL	MP:0003944	abnormal T cell subpopulation ratio	CCO:MP0003944
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(CD4-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0005091	increased double-positive T cell number	CCO:MP0005091
MGI:1346858	Mapk1	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Tg(CD4-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:1346858	Mapk1	"Mapk1<tm1Melo>/Mapk1<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: 129S2/SvPas * C3H * C57BL/6 * FVB/N	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1346858	Mapk1	"Mapk1<tm1Melo>/Mapk1<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: 129S2/SvPas * C3H * C57BL/6 * FVB/N	MP:0003808	increased endocardial cushion size	CCO:MP0003808
MGI:1346858	Mapk1	"Mapk1<tm1Melo>/Mapk1<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: 129S2/SvPas * C3H * C57BL/6 * FVB/N	MP:0001785	edema	CCO:MP0001785
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<+>	involves: C57BL/6	MP:0005140	decreased cardiac muscle contractility	CCO:MP0005140
MGI:1346858	Mapk1	"Mapk1<tm1Melo>/Mapk1<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: 129S2/SvPas * C3H * C57BL/6 * FVB/N	MP:0001654	hepatic necrosis	CCO:MP0001654
MGI:1346858	Mapk1	"Mapk1<tm1Melo>/Mapk1<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: 129S2/SvPas * C3H * C57BL/6 * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346858	Mapk1	"Mapk1<tm1Melo>/Mapk1<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: 129S2/SvPas * C3H * C57BL/6 * FVB/N	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<+>	involves: C57BL/6	MP:0003037	increased infarction size	CCO:MP0003037
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<+>	involves: C57BL/6	MP:0003222	increased cardiomyocyte apoptosis	CCO:MP0003222
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<+>	involves: C57BL/6	MP:0003393	decreased cardiac output	CCO:MP0003393
MGI:1346858	Mapk1	"Mapk1<tm1Gela>/Mapk1<tm1Gela>,Tg(GFAP-cre)25Mes/0"	involves: 129 * FVB/N	MP:0006254	thin cerebral cortex	CCO:MP0006254
MGI:1346858	Mapk1	Mapk1<tm1Kuta>/Mapk1<tm1Kuta>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:1346858	Mapk1	"Mapk1<tm2Moga>/Mapk1<tm2Moga>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Mx1-cre)1Cgn/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005432	abnormal pro-B cell morphology	CCO:MP0005432
MGI:1346858	Mapk1	"Mapk1<tm1Gela>/Mapk1<tm1Gela>,Tg(GFAP-cre)25Mes/0"	involves: 129 * FVB/N	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:1346858	Mapk1	"Mapk1<tm2Moga>/Mapk1<tm2Moga>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Mx1-cre)1Cgn/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008233	abnormal pro-B cell differentiation	CCO:MP0008233
MGI:1346858	Mapk1	"Mapk1<tm1Melo>/Mapk1<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: 129S2/SvPas * C3H * C57BL/6 * FVB/N	MP:0001544	abnormal cardiovascular system physiology	CCO:MP0001544
MGI:1346858	Mapk1	Mapk1<tm1Kuta>/Mapk1<tm1.1Kuta>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346858	Mapk1	Mapk1<tm1.1Kuta>/Mapk1<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * FVB/N	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1346858	Mapk1	Mapk1<tm1.1Kuta>/Mapk1<+>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * FVB/N	MP:0001265	decreased body size	CCO:MP0001265
MGI:1346858	Mapk1	Mapk1<tm1.1Kuta>/Mapk1<tm1.1Kuta>	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346858	Mapk1	"Mapk1<tm2Moga>/Mapk1<tm2Moga>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Mx1-cre)1Cgn/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:1346858	Mapk1	Mapk1<tm1Kuta>/Mapk1<tm1Kuta>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:1346858	Mapk1	"Mapk1<tm1Gela>/Mapk1<tm1Gela>,Tg(GFAP-cre)25Mes/0"	involves: 129 * FVB/N	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:1346858	Mapk1	"Mapk1<tm1Gela>/Mapk1<tm1Gela>,Tg(GFAP-cre)25Mes/0"	involves: 129 * FVB/N	MP:0001454	abnormal cued conditioning behavior	CCO:MP0001454
MGI:1346858	Mapk1	"Mapk1<tm1Gela>/Mapk1<tm1Gela>,Tg(GFAP-cre)25Mes/0"	involves: 129 * FVB/N	MP:0001469	abnormal contextual conditioning	CCO:MP0001469
MGI:1346858	Mapk1	Mapk1<tm1Kuta>/Mapk1<tm1Kuta>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001454	abnormal cued conditioning behavior	CCO:MP0001454
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<tm1Melo>	involves: 129S2/SvPas * C57BL/6	MP:0001717	absent ectoplacental cone	CCO:MP0001717
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<tm1Melo>	involves: 129S2/SvPas * C57BL/6	MP:0002583	absent extraembryonic ectoderm	CCO:MP0002583
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<tm1Melo>	involves: 129S2/SvPas * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<+>	involves: 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<tm1Melo>	involves: 129S2/SvPas * CD-1	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<tm1Melo>	involves: 129S2/SvPas * CD-1	MP:0002583	absent extraembryonic ectoderm	CCO:MP0002583
MGI:1346858	Mapk1	Mapk1<tm1Melo>/Mapk1<tm1Melo>	involves: 129S2/SvPas * CD-1	MP:0001717	absent ectoplacental cone	CCO:MP0001717
MGI:1346858	Mapk1	Mapk1<tm1Moga>/Mapk1<tm1Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1346858	Mapk1	Mapk1<tm1Moga>/Mapk1<tm1Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346858	Mapk1	Mapk1<tm1Moga>/Mapk1<tm1Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:1346858	Mapk1	Mapk1<tm2Moga>/Mapk1<tm2Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1346858	Mapk1	Mapk1<tm1Moga>/Mapk1<tm1Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:1346858	Mapk1	Mapk1<tm1Moga>/Mapk1<tm1Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0001712	abnormal placenta development	CCO:MP0001712
MGI:1346858	Mapk1	Mapk1<tm2Moga>/Mapk1<tm2Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0001712	abnormal placenta development	CCO:MP0001712
MGI:1346858	Mapk1	Mapk1<tm2Moga>/Mapk1<tm2Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1346858	Mapk1	Mapk1<tm2Moga>/Mapk1<tm2Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346858	Mapk1	Mapk1<tm1Moga>/Mapk1<tm1Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1346858	Mapk1	Mapk1<tm2Moga>/Mapk1<tm2Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0003231	abnormal placenta vasculature	CCO:MP0003231
MGI:1346858	Mapk1	Mapk1<tm2Moga>/Mapk1<tm2Moga>	involves: 129P2/OlaHsd * C57BL/6	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:1353438	Mapk12	"Mapk12<tm1Cnd>/Mapk12<tm1Cnd>,Mapk13<tm1Cnd>/Mapk13<tm1Cnd>"	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1353438	Mapk12	Mapk12<tm1Cnd>/Mapk12<tm1Cnd>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1346864	Mapk13	Mapk13<tm1Cnd>/Mapk13<tm1Cnd>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1346864	Mapk13	"Mapk12<tm1Cnd>/Mapk12<tm1Cnd>,Mapk13<tm1Cnd>/Mapk13<tm1Cnd>"	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1346864	Mapk13	Mapk13<tm2.1Lex>/Mapk13<tm2.1Lex>	B6.129S5-Mapk13<tm2.1Lex>	MP:0003562	abnormal pancreatic beta cell physiology	CCO:MP0003562
MGI:1346864	Mapk13	Mapk13<tm2.1Lex>/Mapk13<tm2.1Lex>	B6.129S5-Mapk13<tm2.1Lex>	MP:0003058	increased insulin secretion	CCO:MP0003058
MGI:1346864	Mapk13	Mapk13<tm2.1Lex>/Mapk13<tm2.1Lex>	B6.129S5-Mapk13<tm2.1Lex>	MP:0005659	increased resistance to diet-induced obesity	CCO:MP0005659
MGI:1346864	Mapk13	Mapk13<tm2.1Lex>/Mapk13<tm2.1Lex>	B6.129S5-Mapk13<tm2.1Lex>	MP:0002891	increased insulin sensitivity	CCO:MP0002891
MGI:1346864	Mapk13	Mapk13<tm2.1Lex>/Mapk13<tm2.1Lex>	B6.129S5-Mapk13<tm2.1Lex>	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:1346864	Mapk13	Mapk13<tm2.1Lex>/Mapk13<tm2.1Lex>	B6.129S5-Mapk13<tm2.1Lex>	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1346864	Mapk13	Mapk13<tm2.1Lex>/Mapk13<tm2.1Lex>	B6.129S5-Mapk13<tm2.1Lex>	MP:0005292	improved glucose tolerance	CCO:MP0005292
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm2Nbr>/Mapk14<+>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm2Nbr>/Mapk14<+>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm2Nbr>/Mapk14<+>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0006372	impaired placental function	CCO:MP0006372
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0005140	decreased cardiac muscle contractility	CCO:MP0005140
MGI:1346865	Mapk14	"Mapk14<tm1Dvb>/Mapk14<+>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0008014	lung tumor	CCO:MP0008014
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003038	decreased infarction size	CCO:MP0003038
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<+>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000343	altered response to myocardial infarction	CCO:MP0000343
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0008788	abnormal fetal cardiomyocyte morphology	CCO:MP0008788
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0003717	pallor	CCO:MP0003717
MGI:1346865	Mapk14	"Mapk14<tm2Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129 * C57BL/6 * CD-1 * SJL	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1346865	Mapk14	"Mapk14<tm1Dvb>/Mapk14<+>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0005031	abnormal trophoblast layer morphology	CCO:MP0005031
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0000293	absent myocardial trabeculae	CCO:MP0000293
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0001712	abnormal placenta development	CCO:MP0001712
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0001633	poor circulation	CCO:MP0001633
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:1346865	Mapk14	Mapk14<tm1Gab>/Mapk14<tm1Gab>	involves: DBA/1LacJ	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1346865	Mapk14	Mapk14<tm1Nbr>/Mapk14<tm1Nbr>	either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)	MP:0003231	abnormal placenta vasculature	CCO:MP0003231
MGI:1346865	Mapk14	"Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0008014	lung tumor	CCO:MP0008014
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0001176	abnormal lung development	CCO:MP0001176
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1346865	Mapk14	"Mapk14<tm2Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129 * C57BL/6 * CD-1 * SJL	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:1346865	Mapk14	"Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1346865	Mapk14	"Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1346865	Mapk14	"Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0001176	abnormal lung development	CCO:MP0001176
MGI:1346865	Mapk14	"Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:1346865	Mapk14	"Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:1346865	Mapk14	"Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1346865	Mapk14	"Mapk14<tm2Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129 * C57BL/6 * CD-1 * SJL	MP:0006382	abnormal lung epithelium morphology	CCO:MP0006382
MGI:1346865	Mapk14	"Mapk14<tm2Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129 * C57BL/6 * CD-1 * SJL	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1346865	Mapk14	"Mapk14<tm2Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129 * C57BL/6 * CD-1 * SJL	MP:0002273	abnormal respiratory alveolar epithelial cell morphology	CCO:MP0002273
MGI:1346865	Mapk14	"Kras<tm1Bbd>/Kras<+>,Mapk14<tm1Nbr>/Mapk14<tm2Nbr>,Tg(CMV-cre/ESR1)1Ipc/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:1346865	Mapk14	Mapk14<tm1Jda>/Mapk14<tm1Jda>	B6.Cg-Mapk14<tm1Jda>	MP:0005465	abnormal T-helper 1 physiology	CCO:MP0005465
MGI:1346865	Mapk14	Mapk14<tm1Jda>/Mapk14<tm1Jda>	B6.Cg-Mapk14<tm1Jda>	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:1346865	Mapk14	Mapk14<tm1Jda>/Mapk14<tm1Jda>	B6.Cg-Mapk14<tm1Jda>	MP:0008563	decreased interferon-alpha secretion	CCO:MP0008563
MGI:1346865	Mapk14	Mapk14<tm1Jda>/Mapk14<tm1Jda>	B6.Cg-Mapk14<tm1Jda>	MP:0008567	decreased interferon-gamma secretion	CCO:MP0008567
MGI:1346865	Mapk14	Mapk14<tm1Okee>/Mapk14<tm1Okee>	involves: 129S/SvEv * C57BL/6	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:1346865	Mapk14	Mapk14<tm1Jda>/Mapk14<tm1Jda>	B6.Cg-Mapk14<tm1Jda>	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000601	small liver	CCO:MP0000601
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001577	anemia	CCO:MP0001577
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003717	pallor	CCO:MP0003717
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1346865	Mapk14	Mapk14<tm1Mka>/Mapk14<tm1Mka>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0000603	pale liver	CCO:MP0000603
MGI:1346865	Mapk14	"Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Myh6-cre)2182Mds/0"	involves: C57BL/6J	MP:0004485	increased response of heart to induced stress	CCO:MP0004485
MGI:1346865	Mapk14	"Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Myh6-cre)2182Mds/0"	involves: C57BL/6J	MP:0003222	increased cardiomyocyte apoptosis	CCO:MP0003222
MGI:1346865	Mapk14	"Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Myh6-cre)2182Mds/0"	involves: C57BL/6J	MP:0003141	cardiac fibrosis	CCO:MP0003141
MGI:1346865	Mapk14	"Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Myh6-cre)2182Mds/0"	involves: C57BL/6J	MP:0002833	increased heart weight	CCO:MP0002833
MGI:1346865	Mapk14	"Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Myh6-cre)2182Mds/0"	involves: C57BL/6J	MP:0000274	enlarged heart	CCO:MP0000274
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346865	Mapk14	"Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Myh6-cre)2182Mds/0"	involves: C57BL/6J	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:1346865	Mapk14	Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>	involves: C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1346865	Mapk14	"Mapk14<tm1.2Otsu>/Mapk14<tm1.2Otsu>,Tg(Myh6-cre)2182Mds/0"	involves: C57BL/6J	MP:0005140	decreased cardiac muscle contractility	CCO:MP0005140
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1346865	Mapk14	"Mapk14<tm1Lex>/Mapk14<tm1Lex>,Myl7<tm1(cre)Krc>/Myl7<+>"	involves: 129S1/Sv * 129S5/SvEvBrd * 129X1/SvJ * C57BL/6	MP:0003567	abnormal fetal cardiomyocyte proliferation	CCO:MP0003567
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000260	abnormal angiogenesis	CCO:MP0000260
MGI:1346865	Mapk14	Mapk14<tm1.1Otsu>/Mapk14<tm1.1Otsu>	involves: C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001713	decreased trophoblast giant cell number	CCO:MP0001713
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003403	absent placental labyrinth	CCO:MP0003403
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004076	abnormal vitelline vascular remodeling	CCO:MP0004076
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004255	abnormal spongiotrophoblast layer morphology	CCO:MP0004255
MGI:1346865	Mapk14	Mapk14<tm1Mms>/Mapk14<tm1Mms>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:1346859	Mapk3	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0005094	abnormal T cell proliferation	CCO:MP0005094
MGI:1346859	Mapk3	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0000706	small thymus	CCO:MP0000706
MGI:1346859	Mapk3	Mapk3<tm1Tgf>/Mapk3<tm1Tgf>	either: 129-Mapk3<tm1Tgf> or B6.129-Mapk3<tm1Tgf>	MP:0004799	increased susceptibility to experimental autoimmune encephalomyelitis	CCO:MP0004799
MGI:1346859	Mapk3	Mapk3<tm1Tgf>/Mapk3<tm1Tgf>	either: 129-Mapk3<tm1Tgf> or B6.129-Mapk3<tm1Tgf>	MP:0003009	abnormal cytokine secretion	CCO:MP0003009
MGI:1346859	Mapk3	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CD4-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0004919	abnormal positive T cell selection	CCO:MP0004919
MGI:1346859	Mapk3	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CD4-cre)1Cwi/0,Tg(TcrAND)53Hed/0"	involves: C57BL/6 * DBA/2 * SJL	MP:0003944	abnormal T cell subpopulation ratio	CCO:MP0003944
MGI:1346859	Mapk3	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(TcraTcrb)1100Mjb/0"	involves: C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1346859	Mapk3	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CD4-cre)1Cwi/0,Tg(TcrAND)53Hed/0"	involves: C57BL/6 * DBA/2 * SJL	MP:0004919	abnormal positive T cell selection	CCO:MP0004919
MGI:1346859	Mapk3	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0005091	increased double-positive T cell number	CCO:MP0005091
MGI:1346859	Mapk3	"Mapk1<tm1Hed>/Mapk1<tm1Hed>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Lck-cre)1Cwi/0"	involves: C57BL/6 * DBA/2	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1346859	Mapk3	"Mapk3<tm1Gpg>/Mapk3<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: C3H * C57BL/6 * FVB/N	MP:0003808	increased endocardial cushion size	CCO:MP0003808
MGI:1346859	Mapk3	"Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: C3H * C57BL/6 * FVB/N	MP:0001785	edema	CCO:MP0001785
MGI:1346859	Mapk3	"Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: C3H * C57BL/6 * FVB/N	MP:0001654	hepatic necrosis	CCO:MP0001654
MGI:1346859	Mapk3	"Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: C3H * C57BL/6 * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346859	Mapk3	"Mapk3<tm1Gpg>/Mapk3<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: C3H * C57BL/6 * FVB/N	MP:0001785	edema	CCO:MP0001785
MGI:1346859	Mapk3	"Mapk3<tm1Gpg>/Mapk3<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: C3H * C57BL/6 * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346859	Mapk3	"Mapk1<tm2Moga>/Mapk1<tm2Moga>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Mx1-cre)1Cgn/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005432	abnormal pro-B cell morphology	CCO:MP0005432
MGI:1346859	Mapk3	"Mapk1<tm2Moga>/Mapk1<tm2Moga>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Mx1-cre)1Cgn/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008233	abnormal pro-B cell differentiation	CCO:MP0008233
MGI:1346859	Mapk3	"Mapk1<tm2Moga>/Mapk1<tm2Moga>,Mapk3<tm1Gpg>/Mapk3<tm1Gpg>,Tg(Mx1-cre)1Cgn/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:1346859	Mapk3	"Mapk3<tm1Gpg>/Mapk3<+>,Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0,Tg(Tek-cre)12Flv/0"	involves: C3H * C57BL/6 * FVB/N	MP:0001654	hepatic necrosis	CCO:MP0001654
MGI:1346859	Mapk3	Mapk3<tm1Gpg>/Mapk3<tm1Gpg>	involves: C57BL/6	MP:0002798	abnormal active avoidance behavior	CCO:MP0002798
MGI:1346859	Mapk3	Mapk3<tm1Gpg>/Mapk3<tm1Gpg>	involves: C57BL/6	MP:0001473	reduced long term potentiation	CCO:MP0001473
MGI:1346859	Mapk3	Mapk3<tm1Gpg>/Mapk3<tm1Gpg>	involves: C57BL/6	MP:0001399	hyperactivity	CCO:MP0001399
MGI:1346859	Mapk3	Mapk3<tm1Gpg>/Mapk3<tm1Gpg>	Not Specified	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:1346859	Mapk3	Mapk3<tm1Jsw>/Mapk3<tm1Jsw>	129S1.Cg-Mapk3<tm1Jsw>	MP:0001399	hyperactivity	CCO:MP0001399
MGI:1346859	Mapk3	Mapk3<tm1Gpg>/Mapk3<tm1Gpg>	Not Specified	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:1346859	Mapk3	Mapk3<tm1Gpg>/Mapk3<tm1Gpg>	involves: C57BL/6	MP:0002799	abnormal passive avoidance behavior	CCO:MP0002799
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0003974	abnormal endocardium morphology	CCO:MP0003974
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0000259	abnormal vascular development	CCO:MP0000259
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0004787	abnormal dorsal aorta morphology	CCO:MP0004787
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0004076	abnormal vitelline vascular remodeling	CCO:MP0004076
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0000432	abnormal head morphology	CCO:MP0000432
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0000913	abnormal brain development	CCO:MP0000913
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0000260	abnormal angiogenesis	CCO:MP0000260
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0001916	intracerebral hemorrhage	CCO:MP0001916
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0003119	abnormal digestive system development	CCO:MP0003119
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0006301	abnormal mesenchyme morphology	CCO:MP0006301
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0004076	abnormal vitelline vascular remodeling	CCO:MP0004076
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0006341	small first branchial arch	CCO:MP0006341
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0002188	small heart	CCO:MP0002188
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0002625	heart left ventricle hypertrophy	CCO:MP0002625
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0000264	failure of vascular branching	CCO:MP0000264
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0003649	decreased heart right ventricle size	CCO:MP0003649
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0003542	abnormal vascular endothelial cell development	CCO:MP0003542
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0005602	decreased angiogenesis	CCO:MP0005602
MGI:1346347	Mapk7	Mapk7<tm1Jsca>/Mapk7<tm1Jsca>	either: (involves: BALB/c) or (involves: C57BL/6)	MP:0006344	small second branchial arch	CCO:MP0006344
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0000292	distended pericardial sacs	CCO:MP0000292
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0000295	poorly developed ventricular trabeculae	CCO:MP0000295
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1346347	Mapk7	Mapk7<tm1Wnt>/Mapk7<tm1Wnt>	involves: C57BL/6	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:1346347	Mapk7	Mapk7<tm1.1Jdl>/Mapk7<tm1.1Jdl>	Not Specified	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:1346347	Mapk7	Mapk7<tm1.1Jdl>/Mapk7<tm1.1Jdl>	Not Specified	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346347	Mapk7	Mapk7<tm1.1Jdl>/Mapk7<tm1.1Jdl>	Not Specified	MP:0004201	fetal growth retardation	CCO:MP0004201
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0002083	premature death	CCO:MP0002083
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0001619	abnormal vascular permeability	CCO:MP0001619
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0000259	abnormal vascular development	CCO:MP0000259
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Myhca-cre)1Abel/0"	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1346347	Mapk7	Mapk7<tm1Jdl>/Mapk7<tm1Jdl>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Tek-cre)12Flv/0"	Not Specified	MP:0003974	abnormal endocardium morphology	CCO:MP0003974
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Tek-cre)12Flv/0"	Not Specified	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Tek-cre)12Flv/0"	Not Specified	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Tek-cre)12Flv/0"	Not Specified	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0004566	myocardial fiber degeneration	CCO:MP0004566
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0005191	head tilt	CCO:MP0005191
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0005150	cachexia	CCO:MP0005150
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0000264	failure of vascular branching	CCO:MP0000264
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0001719	absent vitelline blood vessels	CCO:MP0001719
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0001787	pericardial edema	CCO:MP0001787
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0000295	poorly developed ventricular trabeculae	CCO:MP0000295
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0005592	abnormal vascular smooth muscle morphology	CCO:MP0005592
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0005602	decreased angiogenesis	CCO:MP0005602
MGI:1346347	Mapk7	"Mapk7<tm1Jdl>/Mapk7<tm1Jdl>,Tg(Mx1-cre)1Cgn/0"	Not Specified	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0006055	abnormal vascular endothelial cell morphology	CCO:MP0006055
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0003920	abnormal heart right ventricle morphology	CCO:MP0003920
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0004076	abnormal vitelline vascular remodeling	CCO:MP0004076
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0004787	abnormal dorsal aorta morphology	CCO:MP0004787
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0003231	abnormal placenta vasculature	CCO:MP0003231
MGI:1346347	Mapk7	Mapk7<tm1Kda>/Mapk7<tm1Kda>	involves: 129S6/SvEvTac	MP:0004251	failure of looping morphogenesis	CCO:MP0004251
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0001951	abnormal breathing	CCO:MP0001951
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0002083	premature death	CCO:MP0002083
MGI:105380	Mcm2	Mcm2<tm2Scpr>/Mcm2<tm2Scpr>	involves: 129S6/SvEvTac	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0001402	hypoactivity	CCO:MP0001402
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0001505	hunched posture	CCO:MP0001505
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0000415	partial hair loss	CCO:MP0000415
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0000747	muscle weakness	CCO:MP0000747
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0005454	decreased adipose tissue amount	CCO:MP0005454
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0004275	abnormal postnatal subventricular zone morphology	CCO:MP0004275
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0004841	abnormal small intestine crypts of Lieberkuhn morphology	CCO:MP0004841
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0008108	abnormal small intestinal villus morphology	CCO:MP0008108
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:105380	Mcm2	Mcm2<tm1(cre)Scpr>/Mcm2<tm1(cre)Scpr>	involves: 129S6/SvEvTac	MP:0002075	abnormal coat/hair pigmentation	CCO:MP0002075
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0004816	abnormal class switch recombination	CCO:MP0004816
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0003992	increased mortality induced by ionizing radiation	CCO:MP0003992
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0000706	small thymus	CCO:MP0000706
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0001935	decreased litter size	CCO:MP0001935
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:3525201	Mdc1	Mdc1<Gt(OST441263)Lex>/Mdc1<Gt(OST441263)Lex>	involves: 129 * C57BL/6	MP:0000692	small spleen	CCO:MP0000692
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<+>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:96952	Mdm2	Mdm2<tm1.1Mep>/Mdm2<tm1.1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003918	decreased kidney weight	CCO:MP0003918
MGI:96952	Mdm2	Mdm2<tm1Mep>/Mdm2<tm1.1Mep>	involves: 129S7/SvEvBrd * C57BL/6 * FVB	MP:0001262	decreased body weight	CCO:MP0001262
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003402	decreased liver weight	CCO:MP0003402
MGI:96952	Mdm2	Mdm2<tm1Mep>/Mdm2<tm1.1Mep>	involves: 129S7/SvEvBrd * C57BL/6 * FVB	MP:0003402	decreased liver weight	CCO:MP0003402
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<+>	B6.129S7-Mdm2<tm1Bay>	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm1Glo>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96952	Mdm2	"Mdm2<tm1Bay>/Mdm2<tm1Mep>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:96952	Mdm2	Mdm2<tm1Mep>/Mdm2<tm1.1Mep>	involves: 129S7/SvEvBrd * C57BL/6 * FVB	MP:0003918	decreased kidney weight	CCO:MP0003918
MGI:96952	Mdm2	Mdm2<tm1Mep>/Mdm2<tm1.1Mep>	involves: 129S7/SvEvBrd * C57BL/6 * FVB	MP:0004953	decreased spleen weight	CCO:MP0004953
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004953	decreased spleen weight	CCO:MP0004953
MGI:96952	Mdm2	Mdm2<tm1Mep>/Mdm2<tm1.1Mep>	involves: 129S7/SvEvBrd * C57BL/6 * FVB	MP:0004956	decreased thymus weight	CCO:MP0004956
MGI:96952	Mdm2	"Mdm2<tm1Bay>/Mdm2<tm1Mep>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:96952	Mdm2	"Mdm2<tm1Bay>/Mdm2<tm1Mep>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:96952	Mdm2	Mdm2<tm1Mep>/Mdm2<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<+>,Trp53<tm3Wahl>/Trp53<tm3Wahl>"	involves: 129S4/SvJae * 129S7/SvEvBrd	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<+>,Mdm4<Gt(VICTR20)7Lex>/Mdm4<+>,Trp53<tm3Wahl>/Trp53<tm3Wahl>"	involves: 129	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1.1Mep>	involves: 129S7/SvEvBrd * C57BL/6 * FVB	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000334	decreased granulocyte number	CCO:MP0000334
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002144	abnormal B cell differentiation	CCO:MP0002144
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<+>,Mdm4<Gt(VICTR20)7Lex>/Mdm4<+>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm1Glo>,Trp53<tm3Wahl>/Trp53<tm3Wahl>"	involves: 129S4/SvJae * 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004956	decreased thymus weight	CCO:MP0004956
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008215	decreased immature B cell number	CCO:MP0008215
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000222	decreased neutrophil cell number	CCO:MP0000222
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Mep>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000694	spleen hypoplasia	CCO:MP0000694
MGI:96952	Mdm2	Mdm2<tm1Ypz>/Mdm2<tm1Ypz>	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:96952	Mdm2	Mdm2<tm1Ypz>/Mdm2<tm1Ypz>	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	MP:0001695	abnormal gastrulation	CCO:MP0001695
MGI:96952	Mdm2	Mdm2<tm1Ypz>/Mdm2<tm1Ypz>	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:96952	Mdm2	"Mdm2<tm1Ypz>/Mdm2<tm1Ypz>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6 * FVB/N	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:96952	Mdm2	Mdm2<tm1Ypz>/Mdm2<tm1Ypz>	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm1Glo>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96952	Mdm2	"Mdm2<tm1Bay>/Mdm2<tm1Bay>,Trp53<tm1Snj>/Trp53<tm1Snj>"	involves: C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96952	Mdm2	Mdm2<Gt(Ex65)Byg>/Mdm2<Gt(Ex65)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:96952	Mdm2	Mdm2<tm1Glo>/Mdm2<tm2Glo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Bay>	involves: 129S7/SvEvBrd	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:96952	Mdm2	"Mdm2<tm1Bay>/Mdm2<tm1Bay>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96952	Mdm2	Mdm2<tm1Glo>/Mdm2<tm1Glo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:96952	Mdm2	Mdm2<tm1Glo>/Mdm2<tm1Glo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:96952	Mdm2	Mdm2<tm2.1Glo>/Mdm2<tm2.1Glo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96952	Mdm2	Mdm2<tm1Bay>/Mdm2<tm1Bay>	involves: 129S7/SvEvBrd	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:96952	Mdm2	Mdm2<tm2.3Glo>/Mdm2<tm2.3Glo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96952	Mdm2	Mdm2<tm1Snj>/Mdm2<tm1Bay>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96952	Mdm2	Mdm2<tm1Snj>/Mdm2<tm1Snj>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96952	Mdm2	Mdm2<tm1Glo>/Mdm2<tm2.1Glo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0003222	increased cardiomyocyte apoptosis	CCO:MP0003222
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0002188	small heart	CCO:MP0002188
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0002128	abnormal blood circulation	CCO:MP0002128
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0001544	abnormal cardiovascular system physiology	CCO:MP0001544
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0001914	hemorrhage	CCO:MP0001914
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm1Glo>,Trp53<tm3.1Glo>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:96952	Mdm2	"Mdm2<tm1Glo>/Mdm2<tm2.1Glo>,Tg(Myh6-cre)2182Mds/0"	involves: 129S7/SvEvBrd * FVB/N	MP:0005294	abnormal heart ventricle morphology	CCO:MP0005294
MGI:3028590	Mei1	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	MP:0005159	azoospermia	CCO:MP0005159
MGI:3028590	Mei1	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:3028590	Mei1	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:3028590	Mei1	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:3028590	Mei1	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	MP:0001147	small testis	CCO:MP0001147
MGI:3028590	Mei1	Mei1<m1Jcs>/Mei1<m1Jcs>	involves: 129S1/Sv * C57BL/6J	MP:0001926	female infertility	CCO:MP0001926
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0001869	pancreas inflammation	CCO:MP0001869
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0002031	adrenal tumor	CCO:MP0002031
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0002038	carcinoma	CCO:MP0002038
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003365	glucagonoma	CCO:MP0003365
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003493	parathyroid gland hyperplasia	CCO:MP0003493
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003498	thyroid gland hyperplasia	CCO:MP0003498
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003495	parathyroid adenoma	CCO:MP0003495
MGI:1316736	Men1	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003495	parathyroid adenoma	CCO:MP0003495
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * FVB/N	MP:0003495	parathyroid adenoma	CCO:MP0003495
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<tm1Ctre>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0008000	ovary tumor	CCO:MP0008000
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0009043	pancreas adenoma	CCO:MP0009043
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0009044	adrenal gland adenoma	CCO:MP0009044
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0009592	Leydig cell tumor	CCO:MP0009592
MGI:1316736	Men1	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0000633	abnormal pituitary gland morphology	CCO:MP0000633
MGI:1316736	Men1	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:1316736	Men1	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003498	thyroid gland hyperplasia	CCO:MP0003498
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0003505	prolactinoma	CCO:MP0003505
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0001152	Leydig cell hyperplasia	CCO:MP0001152
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0003495	parathyroid adenoma	CCO:MP0003495
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0003496	thyroid adenoma	CCO:MP0003496
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0003505	prolactinoma	CCO:MP0003505
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0009146	abnormal pancreatic acinar cell morphology	CCO:MP0009146
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * FVB/N	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0009153	pancreas tumor	CCO:MP0009153
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0000633	abnormal pituitary gland morphology	CCO:MP0000633
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0000681	abnormal thyroid gland morphology	CCO:MP0000681
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<tm1.1Ctre>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0009153	pancreas tumor	CCO:MP0009153
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<tm1Ctre>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0001944	abnormal pancreas morphology	CCO:MP0001944
MGI:1316736	Men1	Men1<tm1.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<tm1Ctre>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0003935	abnormal craniofacial development	CCO:MP0003935
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<tm1Ctre>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0009148	pancreas necrosis	CCO:MP0009148
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0006079	stomach tumor	CCO:MP0006079
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0008000	ovary tumor	CCO:MP0008000
MGI:1316736	Men1	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0009592	Leydig cell tumor	CCO:MP0009592
MGI:1316736	Men1	Men1<tm2.1Gfk>/Men1<+>	involves: 129T2/SvEms * C57BL/6	MP:0009043	pancreas adenoma	CCO:MP0009043
MGI:1316736	Men1	Men1<tm1Ctre>/Men1<+>	either: (involves: 129S6/SvEvTac * FVB/N) or (involves: 129S6/SvEvTac * Black Swiss * FVB/N)	MP:0001944	abnormal pancreas morphology	CCO:MP0001944
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0002693	abnormal pancreas physiology	CCO:MP0002693
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0008014	lung tumor	CCO:MP0008014
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0009171	enlarged pancreatic islets	CCO:MP0009171
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<+>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1316736	Men1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0003495	parathyroid adenoma	CCO:MP0003495
MGI:1316736	Men1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * FVB/N	MP:0008014	lung tumor	CCO:MP0008014
MGI:1316736	Men1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1316736	Men1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0009153	pancreas tumor	CCO:MP0009153
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * FVB/N	MP:0009153	pancreas tumor	CCO:MP0009153
MGI:1316736	Men1	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1316736	Men1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:1316736	Men1	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<tm1.1Ctre>"	involves: 129/Sv * 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1316736	Men1	"Men1<tm1Gfk>/Men1<tm1Gfk>,Tg(Ins2-cre)25Mgn/0"	involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA	MP:0009153	pancreas tumor	CCO:MP0009153
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * C57BL/6	MP:0006262	testis tumor	CCO:MP0006262
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1316736	Men1	"Men1<tm1Gfk>/Men1<tm1Gfk>,Tg(Ins2-cre)25Mgn/0"	involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA	MP:0003505	prolactinoma	CCO:MP0003505
MGI:1316736	Men1	"Men1<tm1Gfk>/Men1<tm1Gfk>,Tg(Ins2-cre)25Mgn/0"	involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<tm1.1Ctre>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1316736	Men1	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0006262	testis tumor	CCO:MP0006262
MGI:1316736	Men1	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1316736	Men1	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:1316736	Men1	Men1<tm1.1Ctre>/Men1<+>	involves: 129S6/SvEvTac * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1316736	Men1	"Men1<tm1Gfk>/Men1<tm1Gfk>,Tg(Ins2-cre)25Mgn/0"	involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1316736	Men1	"Cdkn1b<tm1Ako>/Cdkn1b<tm1Ako>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1316736	Men1	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0006262	testis tumor	CCO:MP0006262
MGI:1316736	Men1	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0008014	lung tumor	CCO:MP0008014
MGI:1316736	Men1	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<+>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0009308	adenocarcinoma	CCO:MP0009308
MGI:1316736	Men1	"Cdkn2c<tm1Yxi>/Cdkn2c<tm1Yxi>,Men1<tm1.1Ctre>/Men1<tm1.1Ctre>"	involves: 129/Sv * 129S6/SvEvTac * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1316736	Men1	"Men1<tm1.2Ctre>/Men1<tm1.2Ctre>,Tg(PTH-cre)4167Slib/0"	Not Specified	MP:0000194	hypercalcemia	CCO:MP0000194
MGI:1316736	Men1	Men1<tm1.1Zqw>/Men1<tm1.1Zqw>	involves: 129/Ola * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1316736	Men1	Men1<tm1.1Zqw>/Men1<tm1.1Zqw>	involves: 129/Ola * C57BL/6	MP:0005076	abnormal cell differentiation	CCO:MP0005076
MGI:1316736	Men1	"Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Tg(Ins2-cre)1Herr/0"	Not Specified	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	"Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Tg(Ins2-cre)1Herr/0"	Not Specified	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	"Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Tg(Ins2-cre)1Herr/0"	Not Specified	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:1316736	Men1	"Men1<tm1.2Ctre>/Men1<tm1.2Ctre>,Tg(PTH-cre)4167Slib/0"	Not Specified	MP:0000179	abnormal blood chemistry	CCO:MP0000179
MGI:1316736	Men1	"Men1<tm1.2Ctre>/Men1<tm1.2Ctre>,Tg(PTH-cre)4167Slib/0"	Not Specified	MP:0000678	abnormal parathyroid gland morphology	CCO:MP0000678
MGI:1316736	Men1	Men1<tm1.1Zqw>/Men1<tm1.1Zqw>	involves: 129/Ola * C57BL/6	MP:0003720	abnormal neural tube closure	CCO:MP0003720
MGI:1316736	Men1	"Men1<tm1.2Zqw>/Men1<tm1.2Zqw>,Tg(Ins2-cre)1Herr/0"	Not Specified	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0000597	delayed hepatic development	CCO:MP0000597
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0000295	poorly developed ventricular trabeculae	CCO:MP0000295
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)1Heed/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<+>,Tg(Ins2-cre)1Heed/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)1Heed/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0000914	exencephaly	CCO:MP0000914
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)25Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)25Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)25Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)25Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<+>,Tg(Ins2-cre)1Dh/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0003720	abnormal neural tube closure	CCO:MP0003720
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)1Dh/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)1Dh/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1316736	Men1	Men1<tm1Mmey>/Men1<+>	involves: 129S6/SvEvTac * FVB/N	MP:0003645	increased pancreatic beta cell number	CCO:MP0003645
MGI:1316736	Men1	Men1<tm1Mmey>/Men1<+>	involves: 129S6/SvEvTac * FVB/N	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:1316736	Men1	Men1<tm1Mmey>/Men1<tm1Mmey>	involves: 129S6/SvEvTac * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1316736	Men1	Men1<tm1Zqw>/Men1<tm1Zqw>	either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6)	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<+>,Tg(Ins2-cre)25Mgn/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)1Heed/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)1Dh/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)1Heed/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0003364	insulinoma	CCO:MP0003364
MGI:1316736	Men1	"Men1<tm1Ctre>/Men1<tm1Ctre>,Tg(Ins2-cre)1Dh/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0003364	insulinoma	CCO:MP0003364
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd	MP:0005276	skin tumor	CCO:MP0005276
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0001925	male infertility	CCO:MP0001925
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:101938	Mlh1	Mlh1<tm1Mse>/Mlh1<tm1Mse>	involves: 129S/SvEv	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101938	Mlh1	Mlh1<tm1Mse>/Mlh1<tm1Mse>	involves: 129S/SvEv	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0004208	basal cell carcinoma	CCO:MP0004208
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101938	Mlh1	"Mgmt<tm1Mse>/Mgmt<tm1Mse>,Mlh1<tm1Mse>/Mlh1<tm1Mse>"	involves: 129S/SvEv	MP:0002048	lung adenoma	CCO:MP0002048
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0001926	female infertility	CCO:MP0001926
MGI:101938	Mlh1	Mlh1<tm1Wed>/Mlh1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101938	Mlh1	"Mgmt<tm1Mse>/Mgmt<tm1Mse>,Mlh1<tm1Mse>/Mlh1<tm1Mse>"	involves: 129S/SvEv	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd	MP:0002083	premature death	CCO:MP0002083
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:101938	Mlh1	"Dnmt1<tm1Pwl>/Dnmt1<+>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:101938	Mlh1	"Dnmt1<tm1Pwl>/Dnmt1<+>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0009222	uterus tumor	CCO:MP0009222
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0005276	skin tumor	CCO:MP0005276
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:101938	Mlh1	"Dnmt1<tm1Pwl>/Dnmt1<+>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:101938	Mlh1	"Dnmt1<tm1Jae>/Dnmt1<tm1Pwl>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:101938	Mlh1	"Dnmt1<tm1Jae>/Dnmt1<tm1Pwl>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:101938	Mlh1	"Dnmt1<tm1Jae>/Dnmt1<+>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:101938	Mlh1	"Dnmt1<tm1Jae>/Dnmt1<+>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:101938	Mlh1	"Dnmt1<tm1Jae>/Dnmt1<+>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:101938	Mlh1	"Dnmt1<tm1Pwl>/Dnmt1<+>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:101938	Mlh1	"Dnmt1<tm1Jae>/Dnmt1<+>,Mlh1<tm1Lisk>/Mlh1<tm1Lisk>"	involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	MP:0005159	azoospermia	CCO:MP0005159
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	MP:0001925	male infertility	CCO:MP0001925
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:101938	Mlh1	Mlh1<tm1Rak>/Mlh1<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	MP:0001127	small ovary	CCO:MP0001127
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	MP:0002022	lymphoma	CCO:MP0002022
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	MP:0001926	female infertility	CCO:MP0001926
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	MP:0002680	decreased corpora lutea number	CCO:MP0002680
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:101938	Mlh1	Mlh1<tm1Lisk>/Mlh1<tm1Lisk>	involves: 129S7/SvEvBrd	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:1353455	Mlh3	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	MP:0001925	male infertility	CCO:MP0001925
MGI:1353455	Mlh3	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1353455	Mlh3	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	MP:0005159	azoospermia	CCO:MP0005159
MGI:1353455	Mlh3	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	MP:0001926	female infertility	CCO:MP0001926
MGI:1353455	Mlh3	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	MP:0001147	small testis	CCO:MP0001147
MGI:1353455	Mlh3	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1353455	Mlh3	Mlh3<tm1Lpkn>/Mlh3<tm1Lpkn>	involves: 129S/SvEv	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0008040	decreased NK T cell number	CCO:MP0008040
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0008045	decreased NK cell number	CCO:MP0008045
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002059	abnormal seminal gland morphology	CCO:MP0002059
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0001265	decreased body size	CCO:MP0001265
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0001925	male infertility	CCO:MP0001925
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002463	abnormal neutrophil physiology	CCO:MP0002463
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002415	abnormal neutrophil differentiation	CCO:MP0002415
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0001658	increased mortality induced by gamma-irradiation	CCO:MP0001658
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002594	low mean erythrocyte cell number	CCO:MP0002594
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0008813	decreased common myeloid progenitor cell number	CCO:MP0008813
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002412	increased susceptibility to bacterial infection	CCO:MP0002412
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0000692	small spleen	CCO:MP0000692
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0000694	spleen hypoplasia	CCO:MP0000694
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0000706	small thymus	CCO:MP0000706
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0008208	decreased pro-B cell number	CCO:MP0008208
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0002686	globozoospermia	CCO:MP0002686
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0002217	small lymph nodes	CCO:MP0002217
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0005251	blepharitis	CCO:MP0005251
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0002414	abnormal myeloblast morphology/development	CCO:MP0002414
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0005454	decreased adipose tissue amount	CCO:MP0005454
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0002874	decreased hemoglobin content	CCO:MP0002874
MGI:1924825	Mll5	Mll5<tm1Apa>/Mll5<tm1Apa>	129S6/SvEvTac-Mll5<tm1Apa>	MP:0008111	abnormal granulocyte differentiation	CCO:MP0008111
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0004809	increased hematopoietic stem cell number	CCO:MP0004809
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0004808	abnormal hematopoietic stem cell morphology	CCO:MP0004808
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0000219	increased neutrophil cell number	CCO:MP0000219
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1924825	Mll5	Mll5<tm1Nik>/Mll5<tm1Nik>	B6.Cg-Mll5<tm1Nik>	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0001925	male infertility	CCO:MP0001925
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<+>	B6.129P2-Mll5<tm1.1Hjf>	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<+>	B6.129P2-Mll5<tm1.1Hjf>	MP:0000694	spleen hypoplasia	CCO:MP0000694
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<tm1.1Hjf>	B6.129P2-Mll5<tm1.1Hjf>	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1924825	Mll5	Mll5<tm1.1Hjf>/Mll5<+>	B6.129P2-Mll5<tm1.1Hjf>	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:106207	Mnat1	"Egr2<tm2(cre)Pch>/?,Mnat1<tm2Tpm>/Mnat1<tm2.1Tpm>"	involves: 129S2/SvPas	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:106207	Mnat1	"Egr2<tm2(cre)Pch>/?,Mnat1<tm2Tpm>/Mnat1<tm2.1Tpm>"	involves: 129S2/SvPas	MP:0001406	abnormal gait	CCO:MP0001406
MGI:106207	Mnat1	"Egr2<tm2(cre)Pch>/?,Mnat1<tm2Tpm>/Mnat1<tm2.1Tpm>"	involves: 129S2/SvPas	MP:0000921	demyelination	CCO:MP0000921
MGI:106207	Mnat1	"Egr2<tm2(cre)Pch>/?,Mnat1<tm2Tpm>/Mnat1<tm2.1Tpm>"	involves: 129S2/SvPas	MP:0003961	decreased lean body mass	CCO:MP0003961
MGI:106207	Mnat1	"Egr2<tm2(cre)Pch>/?,Mnat1<tm2Tpm>/Mnat1<tm2.1Tpm>"	involves: 129S2/SvPas	MP:0004074	abnormal Schwann cell precursors	CCO:MP0004074
MGI:106207	Mnat1	Mnat1<tm2Tpm>/Mnat1<tm2Tpm>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:106207	Mnat1	Mnat1<tm1Tpm>/Mnat1<tm1Tpm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:106207	Mnat1	Mnat1<tm1Tpm>/Mnat1<tm1Tpm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:106207	Mnat1	Mnat1<tm1Tpm>/Mnat1<tm1Tpm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1)	MP:0004965	inner cell mass degeneration	CCO:MP0004965
MGI:109150	Mnt	"Mnt<tm1Awb>/Mnt<tm1.1Awb>,Tg(MMTV-cre)4Mam/?"	involves: 129S6/SvEvTac * FVB/N	MP:0000627	abnormal mammary gland morphology	CCO:MP0000627
MGI:109150	Mnt	"Mnt<tm1Awb>/Mnt<tm1.1Awb>,Tg(MMTV-cre)4Mam/?"	involves: 129S6/SvEvTac * FVB/N	MP:0006271	abnormal involution of the mammary gland	CCO:MP0006271
MGI:109150	Mnt	"Mnt<tm1Awb>/Mnt<tm1.1Awb>,Tg(MMTV-cre)4Mam/?"	involves: 129S6/SvEvTac * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:109150	Mnt	Mnt<tm1.1Phu>/Mnt<tm1.1Phu>	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:109150	Mnt	Mnt<tm1.1Phu>/Mnt<tm1.1Phu>	Not Specified	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:109150	Mnt	Mnt<tm1.1Phu>/Mnt<tm1.1Phu>	Not Specified	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:109150	Mnt	"Mnt<tm1Phu>/Mnt<tm1Phu>,Tg(MMTV-cre)4Mam/?"	Not Specified	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:109150	Mnt	Mnt<tm1.1Phu>/Mnt<tm1.1Phu>	Not Specified	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:109150	Mnt	Mnt<tm1.1Phu>/Mnt<tm1.1Phu>	Not Specified	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	129S6/SvEvTac	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	129S6/SvEvTac	MP:0009703	decreased birth body size	CCO:MP0009703
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0009703	decreased birth body size	CCO:MP0009703
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	129S6/SvEvTac	MP:0009546	absent gastric milk in neonates	CCO:MP0009546
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	129S6/SvEvTac	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0005352	small skull	CCO:MP0005352
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0000111	cleft palate	CCO:MP0000111
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0001731	abnormal postnatal growth	CCO:MP0001731
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0004476	absent palatine bone	CCO:MP0004476
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0004441	small occipital bone	CCO:MP0004441
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0005274	abnormal viscerocranium morphology	CCO:MP0005274
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	129S6/SvEvTac	MP:0001731	abnormal postnatal growth	CCO:MP0001731
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0004592	small mandible	CCO:MP0004592
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0009546	absent gastric milk in neonates	CCO:MP0009546
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0004384	small interparietal bone	CCO:MP0004384
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0000074	abnormal neurocranium morphology	CCO:MP0000074
MGI:109150	Mnt	Mnt<tm1.1Awb>/Mnt<tm1.1Awb>	involves: 129S6/SvEvTac * FVB/N	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1100512	Mre11a	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Mre11a<tm1Jpt>/Mre11a<tm1Jpt>"	involves: 129 * 129S7/SvEvBrd	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1100512	Mre11a	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1100512	Mre11a	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0001393	ataxia	CCO:MP0001393
MGI:1100512	Mre11a	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Mre11a<tm1Jpt>/Mre11a<tm1Jpt>"	involves: 129 * 129S7/SvEvBrd	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm2.1Dof>	involves: 129S6/SvEvTac	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm1Dof>	involves: 129S6/SvEvTac	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm1Dof>	involves: 129S6/SvEvTac	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm1Dof>	involves: 129S6/SvEvTac	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm1Dof>	involves: 129S6/SvEvTac	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm2.1Dof>	involves: 129S6/SvEvTac	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm2.1Dof>	involves: 129S6/SvEvTac	MP:0004030	induced chromosome breakage	CCO:MP0004030
MGI:1100512	Mre11a	Mre11a<tm2.1Dof>/Mre11a<tm2.2Dof>	Not Specified	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm2.1Dof>	involves: 129S6/SvEvTac	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1100512	Mre11a	Mre11a<tm2.1Dof>/Mre11a<tm2.2Dof>	Not Specified	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1100512	Mre11a	Mre11a<tm2.1Dof>/Mre11a<tm2.2Dof>	Not Specified	MP:0004030	induced chromosome breakage	CCO:MP0004030
MGI:1100512	Mre11a	Mre11a<tm2.1Dof>/Mre11a<tm2.2Dof>	Not Specified	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:1100512	Mre11a	Mre11a<tm2.1Dof>/Mre11a<tm2.2Dof>	Not Specified	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1100512	Mre11a	Mre11a<tm2.1Dof>/Mre11a<tm2.2Dof>	Not Specified	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1100512	Mre11a	Mre11a<tm2.1Dof>/Mre11a<tm2.2Dof>	Not Specified	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1100512	Mre11a	Mre11a<tm1Dof>/Mre11a<tm2.1Dof>	involves: 129S6/SvEvTac	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1100512	Mre11a	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1100512	Mre11a	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:1100512	Mre11a	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004030	induced chromosome breakage	CCO:MP0004030
MGI:1100512	Mre11a	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1100512	Mre11a	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003718	maternal effect	CCO:MP0003718
MGI:1100512	Mre11a	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1100512	Mre11a	Mre11a<tm1Jpt>/Mre11a<tm1Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002396	abnormal hematopoietic system morphology/development	CCO:MP0002396
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1100512	Mre11a	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:101816	Msh2	Msh2<tm1Whl>/Msh2<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005276	skin tumor	CCO:MP0005276
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<tm1Brd>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0005276	skin tumor	CCO:MP0005276
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:101816	Msh2	"Msh2<tm1Tts>/Msh2<tm1Tts>,Nudt1<tm1Tts>/Nudt1<tm1Tts>"	involves: 129S/SvEv * C57BL/6J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:101816	Msh2	Msh2<tm1Whl>/Msh2<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0009320	lymphoblastic lymphoma	CCO:MP0009320
MGI:101816	Msh2	Msh2<tm1Whl>/Msh2<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:101816	Msh2	Msh2<tm1Whl>/Msh2<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101816	Msh2	Msh2<tm1Whl>/Msh2<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:101816	Msh2	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0009320	lymphoblastic lymphoma	CCO:MP0009320
MGI:101816	Msh2	Msh2<tm1Whl>/Msh2<tm1Whl>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:101816	Msh2	Msh2<tm1Htr>/Msh2<tm1Htr>	either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * FVB)	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:101816	Msh2	Msh2<tm1Mtn>/Msh2<tm1Mtn>	involves: C57BL/6	MP:0004816	abnormal class switch recombination	CCO:MP0004816
MGI:101816	Msh2	Msh2<tm1Mak>/Msh2<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:101816	Msh2	Msh2<tm1Mtn>/Msh2<tm1Mtn>	involves: C57BL/6	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:101816	Msh2	Msh2<tm1Mtn>/Msh2<tm1Mtn>	involves: C57BL/6	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:101816	Msh2	Msh2<tm1Mak>/Msh2<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:101816	Msh2	Msh2<tm1Mtn>/Msh2<tm1Mtn>	involves: C57BL/6	MP:0001805	decreased IgG level	CCO:MP0001805
MGI:101816	Msh2	Msh2<tm1Wed>/Msh2<tm1Wed>	involves: 129 * C57BL/6 * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<tm1Mak>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<tm1Mak>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<tm1Mak>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<+>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<+>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<+>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002048	lung adenoma	CCO:MP0002048
MGI:101816	Msh2	Msh2<tm1Wed>/Msh2<tm1Wed>	involves: 129 * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:101816	Msh2	Msh2<tm1Wed>/Msh2<tm1Wed>	involves: 129 * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<+>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<+>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<tm1Mak>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0002048	lung adenoma	CCO:MP0002048
MGI:101816	Msh2	Msh2<tm1Wed>/Msh2<tm1Wed>	involves: 129 * C57BL/6 * SJL	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:101816	Msh2	"Msh2<tm1Mak>/Msh2<+>,Mutyh<tm1Jhmi>/Mutyh<tm1Jhmi>,Ogg1<tm1Tld>/Ogg1<tm1Tld>"	involves: 129 * C57BL/6J	MP:0008000	ovary tumor	CCO:MP0008000
MGI:1860077	Msh4	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1860077	Msh4	"Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>"	involves: 129/Sv * C57BL/6 * SJL	MP:0001925	male infertility	CCO:MP0001925
MGI:1860077	Msh4	"Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>"	involves: 129/Sv * C57BL/6 * SJL	MP:0001926	female infertility	CCO:MP0001926
MGI:1860077	Msh4	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	MP:0002209	decreased germ cell number	CCO:MP0002209
MGI:1860077	Msh4	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1860077	Msh4	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	MP:0001926	female infertility	CCO:MP0001926
MGI:1860077	Msh4	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1860077	Msh4	"Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>"	involves: 129/Sv * C57BL/6 * SJL	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1860077	Msh4	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	MP:0005159	azoospermia	CCO:MP0005159
MGI:1860077	Msh4	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	MP:0001925	male infertility	CCO:MP0001925
MGI:1860077	Msh4	Msh4<tm1Wed>/Msh4<tm1Wed>	involves: 129/Sv * C57BL/6 * SJL	MP:0001127	small ovary	CCO:MP0001127
MGI:1329021	Msh5	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1329021	Msh5	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1329021	Msh5	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1329021	Msh5	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0001147	small testis	CCO:MP0001147
MGI:1329021	Msh5	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0001926	female infertility	CCO:MP0001926
MGI:1329021	Msh5	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0005159	azoospermia	CCO:MP0005159
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0004805	absent oocytes	CCO:MP0004805
MGI:1329021	Msh5	"Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>"	involves: 129/Sv * C57BL/6 * SJL	MP:0001926	female infertility	CCO:MP0001926
MGI:1329021	Msh5	"Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>"	involves: 129/Sv * C57BL/6 * SJL	MP:0001925	male infertility	CCO:MP0001925
MGI:1329021	Msh5	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0001925	male infertility	CCO:MP0001925
MGI:1329021	Msh5	Msh5<tm1Rak>/Msh5<tm1Rak>	involves: 129/Sv * C57BL/6J * SJL	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1329021	Msh5	"Msh4<tm1Wed>/Msh4<tm1Wed>,Msh5<tm1Rak>/Msh5<tm1Rak>"	involves: 129/Sv * C57BL/6 * SJL	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0005159	azoospermia	CCO:MP0005159
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0001925	male infertility	CCO:MP0001925
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0001926	female infertility	CCO:MP0001926
MGI:1329021	Msh5	Msh5<tm1Htr>/Msh5<tm1Htr>	involves: 129P2/OlaHsd * FVB	MP:0001127	small ovary	CCO:MP0001127
MGI:2146005	Mtbp	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2146005	Mtbp	"Mtbp<tm1Glo>/Mtbp<tm1Glo>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2146005	Mtbp	"Mtbp<tm1Glo>/Mtbp<tm1Glo>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2146005	Mtbp	Mtbp<tm1Glo>/Mtbp<tm1Glo>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2146005	Mtbp	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:2146005	Mtbp	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:2146005	Mtbp	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002026	leukemia	CCO:MP0002026
MGI:2146005	Mtbp	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:97249	Myb	Myb<tm1.1Jof>/Myb<tm1.1Jof>	involves: 129/Sv * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97249	Myb	Myb<tm1.1Cgn>/Myb<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0008211	decreased mature B cell number	CCO:MP0008211
MGI:97249	Myb	Myb<tm1.1Cgn>/Myb<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:97249	Myb	Myb<tm1.1Cgn>/Myb<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0004978	decreased B-1 B cell number	CCO:MP0004978
MGI:97249	Myb	Myb<tm1.1Cgn>/Myb<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0001802	arrested B cell differentiation	CCO:MP0001802
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Ssp>	involves: 129/Sv * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Ssp>	involves: 129/Sv * C57BL/6	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Ssp>	involves: 129/Sv * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Ssp>	involves: 129/Sv * C57BL/6	MP:0002414	abnormal myeloblast morphology/development	CCO:MP0002414
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Ssp>	involves: 129/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Ssp>	involves: 129/Sv * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Ssp>	involves: 129/Sv * C57BL/6	MP:0000596	abnormal liver development	CCO:MP0000596
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0008254	increased megakaryocyte cell number	CCO:MP0008254
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0002414	abnormal myeloblast morphology/development	CCO:MP0002414
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0002407	abnormal double-negative T cell morphology	CCO:MP0002407
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0002144	abnormal B cell differentiation	CCO:MP0002144
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0000596	abnormal liver development	CCO:MP0000596
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Ssp>	involves: 129/Sv * C57BL/6	MP:0008254	increased megakaryocyte cell number	CCO:MP0008254
MGI:97249	Myb	Myb<tm1Ssp>/Myb<tm1Ssp>	involves: 129P2/OlaHsd * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97249	Myb	Myb<tm1Ssp>/Myb<tm1Ssp>	involves: 129P2/OlaHsd * CD-1	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97249	Myb	Myb<tm1Ssp>/Myb<tm1Ssp>	involves: 129P2/OlaHsd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:97249	Myb	Myb<tm1Ssp>/Myb<tm1Ssp>	involves: 129P2/OlaHsd * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97249	Myb	Myb<tm1Jof>/Myb<tm1Jof>	involves: 129/Sv * C57BL/6	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:97249	Myb	Myb<tm1Ssp>/Myb<tm1Ssp>	involves: 129P2/OlaHsd * CD-1	MP:0001577	anemia	CCO:MP0001577
MGI:97249	Myb	Myb<tm1Ssp>/Myb<tm1Ssp>	involves: 129P2/OlaHsd * CD-1	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0008470	abnormal spleen B cell follicle morphology	CCO:MP0008470
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0008476	increased spleen red pulp amount	CCO:MP0008476
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<+>"	involves: 129S1/Sv * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<+>"	involves: 129S1/Sv * C57BL/6	MP:0000228	abnormal thrombopoiesis	CCO:MP0000228
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:97249	Myb	"Ep300<tm1Pkb>/Ep300<+>,Myb<tm1Ssp>/Myb<+>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97249	Myb	Myb<tm1.1Cgn>/Myb<tm1.1Cgn>	involves: 129P2/OlaHsd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0000229	abnormal megakaryocyte differentiation	CCO:MP0000229
MGI:97249	Myb	Myb<tm1Cgn>/Myb<tm1.1Cgn>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(CD4-cre)1Cwi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	MP:0008078	increased CD8-positive T cell number	CCO:MP0008078
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<+>"	involves: 129S1/Sv * C57BL/6	MP:0000229	abnormal megakaryocyte differentiation	CCO:MP0000229
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0000228	abnormal thrombopoiesis	CCO:MP0000228
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008347	decreased gamma-delta T cell number	CCO:MP0008347
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0008476	increased spleen red pulp amount	CCO:MP0008476
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<+>"	involves: 129S1/Sv * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<+>"	involves: 129S1/Sv * C57BL/6	MP:0000228	abnormal thrombopoiesis	CCO:MP0000228
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0000229	abnormal megakaryocyte differentiation	CCO:MP0000229
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:97249	Myb	Myb<tm1.1Cgn>/Myb<tm1.1Cgn>	involves: 129P2/OlaHsd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:97249	Myb	"Ep300<tm1Pkb>/Ep300<+>,Myb<tm1Ssp>/Myb<+>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:97249	Myb	"Ep300<tm1Pkb>/Ep300<+>,Myb<tm1Ssp>/Myb<+>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0002417	abnormal megakaryocyte morphology	CCO:MP0002417
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0001825	arrested T cell differentiation	CCO:MP0001825
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0002144	abnormal B cell differentiation	CCO:MP0002144
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0000229	abnormal megakaryocyte differentiation	CCO:MP0000229
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(CD4-cre)1Cwi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<+>"	involves: 129S1/Sv * C57BL/6	MP:0000229	abnormal megakaryocyte differentiation	CCO:MP0000229
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0000228	abnormal thrombopoiesis	CCO:MP0000228
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0002407	abnormal double-negative T cell morphology	CCO:MP0002407
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<+>"	involves: 129S1/Sv * C57BL/6	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(CD4-cre)1Cwi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1.1Cgn>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0000239	absent common myeloid progenitor cells	CCO:MP0000239
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0001802	arrested B cell differentiation	CCO:MP0001802
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0001825	arrested T cell differentiation	CCO:MP0001825
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0000248	macrocytosis	CCO:MP0000248
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<+>"	involves: 129S1/Sv * C57BL/6	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1.1Cgn>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1.1Cgn>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0008083	decreased single-positive T cell number	CCO:MP0008083
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0004809	increased hematopoietic stem cell number	CCO:MP0004809
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0003405	abnormal platelet shape	CCO:MP0003405
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(Lck-cre)548Jxm/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:97249	Myb	Myb<M303V>/Myb<M303V>	involves: 129S1/SvlmJ * C57BL/6	MP:0005012	decreased eosinophil cell number	CCO:MP0005012
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt4>/Myb<Plt4>"	involves: 129S1/Sv * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0008470	abnormal spleen B cell follicle morphology	CCO:MP0008470
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(CD4-cre)1Cwi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:97249	Myb	"Myb<tm1Epr>/Myb<tm1Epr>,Tg(CD4-cre)1Cwi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:97249	Myb	"Mpl<tm1Wsa>/Mpl<tm1Wsa>,Myb<Plt3>/Myb<Plt3>"	involves: 129S1/Sv * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:97249	Myb	"Myb<tm1Cgn>/Myb<tm1Cgn>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:2179432	Mycbp2	"Emx1<tm1(cre)Krj>/Emx1<+>,Mycbp2<tm1Adia>/Mycbp2<tm1Adia>"	involves: 129S2/SvPas * C57BL/6	MP:0000781	decreased corpus callosum size	CCO:MP0000781
MGI:2179432	Mycbp2	"Mycbp2<mgln>/Mycbp2<mgln>,Tg(Isl1-EGFP)2Slp/0"	involves: C3H * C57BL/6 * DBA/2J	MP:0000940	abnormal motor neuron innervation	CCO:MP0000940
MGI:2179432	Mycbp2	"Mycbp2<mgln>/Mycbp2<mgln>,Tg(Mnx1-GFP)1Slp/0"	involves: C3H * C57BL/6 * DBA/2J	MP:0000940	abnormal motor neuron innervation	CCO:MP0000940
MGI:2179432	Mycbp2	"Mycbp2<mgln>/Mycbp2<mgln>,Tg(Isl1-EGFP*)1Slp/0"	B6.Cg-Mycbp2<mgln> Tg(Isl1-EGFP*)1Slp	MP:0003651	abnormal axon outgrowth	CCO:MP0003651
MGI:2179432	Mycbp2	"Mycbp2<mgln>/Mycbp2<mgln>,Tg(Isl1-EGFP*)1Slp/0"	B6.Cg-Mycbp2<mgln> Tg(Isl1-EGFP*)1Slp	MP:0000937	abnormal motor neuron morphology	CCO:MP0000937
MGI:2179432	Mycbp2	"Mycbp2<mgln>/Mycbp2<mgln>,Tg(Isl1-EGFP*)1Slp/0"	B6.Cg-Mycbp2<mgln> Tg(Isl1-EGFP*)1Slp	MP:0000940	abnormal motor neuron innervation	CCO:MP0000940
MGI:2179432	Mycbp2	"Mycbp2<mgln>/Mycbp2<mgln>,Tg(Isl1-EGFP*)1Slp/0"	B6.Cg-Mycbp2<mgln> Tg(Isl1-EGFP*)1Slp	MP:0001077	abnormal spinal nerve morphology	CCO:MP0001077
MGI:2179432	Mycbp2	"Mycbp2<mgln>/Mycbp2<mgln>,Tg(Isl1-EGFP*)1Slp/0"	B6.Cg-Mycbp2<mgln> Tg(Isl1-EGFP*)1Slp	MP:0000965	abnormal sensory neuron morphology	CCO:MP0000965
MGI:2179432	Mycbp2	"Mycbp2<mgln>/Mycbp2<mgln>,Tg(Isl1-EGFP*)1Slp/0"	B6.Cg-Mycbp2<mgln> Tg(Isl1-EGFP*)1Slp	MP:0000967	abnormal sensory neuron projections	CCO:MP0000967
MGI:2179432	Mycbp2	"Ednrb<s-15DttMb>/Ednrb<+>,Mycbp2<tm1.1Adia>/Mycbp2<+>"	involves: 101/Rl * C3H/Rl * C57BL/6 * FVB/N	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:2179432	Mycbp2	"Map3K12<Gt(RRN366)Byg>/Map3K12<Gt(RRN366)Byg>,Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0008129	absent brain internal capsule	CCO:MP0008129
MGI:2179432	Mycbp2	"Map3K12<Gt(RRN366)Byg>/Map3K12<Gt(RRN366)Byg>,Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0008128	abnormal brain internal capsule morphology	CCO:MP0008128
MGI:2179432	Mycbp2	"Map3K12<Gt(RRN366)Byg>/Map3K12<Gt(RRN366)Byg>,Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:2179432	Mycbp2	"Map3K12<Gt(RRN366)Byg>/Map3K12<Gt(RRN366)Byg>,Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0000825	dilated lateral ventricles	CCO:MP0000825
MGI:2179432	Mycbp2	"Mycbp2<magsp>/Mycbp2<magsp>,Tg(Isl1-EGFP*)1Slp/0"	B6.Cg-Mycbp2<magsp> Tg(Isl1-EGFP*)1Slp	MP:0000940	abnormal motor neuron innervation	CCO:MP0000940
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0000832	abnormal thalamus morphology	CCO:MP0000832
MGI:2179432	Mycbp2	"Emx1<tm1(cre)Krj>/Emx1<+>,Mycbp2<tm1Adia>/Mycbp2<tm1Adia>"	involves: 129S2/SvPas * C57BL/6	MP:0002961	abnormal axon guidance	CCO:MP0002961
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0000937	abnormal motor neuron morphology	CCO:MP0000937
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0002279	abnormal diaphragm morphology	CCO:MP0002279
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0000897	abnormal midbrain morphology	CCO:MP0000897
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0001053	abnormal neuromuscular synapse morphology	CCO:MP0001053
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0001078	abnormal phrenic nerve morphology	CCO:MP0001078
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0000781	decreased corpus callosum size	CCO:MP0000781
MGI:2179432	Mycbp2	"Mnx1<tm4(cre)Tmj>/Mnx1<+>,Mycbp2<tm1Adia>/Mycbp2<tm1Adia>"	involves: 129S1/Sv * C57BL/6	MP:0001053	abnormal neuromuscular synapse morphology	CCO:MP0001053
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0000830	abnormal diencephalon morphology	CCO:MP0000830
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0000825	dilated lateral ventricles	CCO:MP0000825
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0002961	abnormal axon guidance	CCO:MP0002961
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0004101	abnormal brain interneuron morphology	CCO:MP0004101
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0003241	loss of cortex neurons	CCO:MP0003241
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0008227	absent anterior commissure	CCO:MP0008227
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0008128	abnormal brain internal capsule morphology	CCO:MP0008128
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0004165	abnormal lateral geniculate nucleus morphology	CCO:MP0004165
MGI:2179432	Mycbp2	"Emx1<tm1(cre)Krj>/Emx1<+>,Mycbp2<tm1Adia>/Mycbp2<tm1Adia>"	involves: 129S2/SvPas * C57BL/6	MP:0000780	abnormal corpus callosum morphology	CCO:MP0000780
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0004082	abnormal habenula morphology	CCO:MP0004082
MGI:2179432	Mycbp2	"Emx1<tm1(cre)Krj>/Emx1<+>,Mycbp2<tm1Adia>/Mycbp2<tm1Adia>"	involves: 129S2/SvPas * C57BL/6	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:2179432	Mycbp2	"Emx1<tm1(cre)Krj>/Emx1<+>,Mycbp2<tm1Adia>/Mycbp2<tm1Adia>"	involves: 129S2/SvPas * C57BL/6	MP:0008535	enlarged lateral ventricles	CCO:MP0008535
MGI:2179432	Mycbp2	"Mnx1<tm4(cre)Tmj>/Mnx1<+>,Mycbp2<tm1Adia>/Mycbp2<tm1Adia>"	involves: 129S1/Sv * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:2179432	Mycbp2	Mycbp2<tm1.1Adia>/Mycbp2<tm1.1Adia>	involves: C57BL/6 * FVB/N	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:2179432	Mycbp2	"Ednrb<s-24Pub>/Ednrb<+>,Mycbp2<m274-4Tpo>/Mycbp2<+>"	involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ	MP:0001954	respiratory distress	CCO:MP0001954
MGI:2179432	Mycbp2	"Ednrb<s-24Pub>/Ednrb<+>,Mycbp2<m274-4Tpo>/Mycbp2<+>"	involves: 101/Rl * C3H/Rl * C57BL/6J * SSL/LeJ	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:2179432	Mycbp2	Mycbp2<m274-4Tpo>/Mycbp2<m274-4Tpo>	involves: C57BL/6J * SSL/LeJ	MP:0009703	decreased birth body size	CCO:MP0009703
MGI:2179432	Mycbp2	Mycbp2<m274-4Tpo>/Mycbp2<m274-4Tpo>	involves: C57BL/6J * SSL/LeJ	MP:0009674	decreased birth weight	CCO:MP0009674
MGI:2179432	Mycbp2	Mycbp2<m274-4Tpo>/Mycbp2<m274-4Tpo>	involves: C57BL/6J * SSL/LeJ	MP:0001954	respiratory distress	CCO:MP0001954
MGI:2179432	Mycbp2	Mycbp2<m274-4Tpo>/Mycbp2<m274-4Tpo>	involves: C57BL/6J * SSL/LeJ	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:2179432	Mycbp2	Mycbp2<m274-4Tpo>/Mycbp2<m274-4Tpo>	involves: C57BL/6J * SSL/LeJ	MP:0001505	hunched posture	CCO:MP0001505
MGI:1930780	Myh10	"Myh10<tm5Rsad>/Myh10<tm5Rsad>,Tg(CMV-cre)1Cgn/0"	involves: 129S/SvEv * BALB/cJ * C57BL/6	MP:0001405	impaired coordination	CCO:MP0001405
MGI:1930780	Myh10	Myh10<tm4Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000822	abnormal brain ventricle morphology	CCO:MP0000822
MGI:1930780	Myh10	"Myh10<tm5Rsad>/Myh10<tm5Rsad>,Tg(CMV-cre)1Cgn/0"	involves: 129S/SvEv * BALB/cJ * C57BL/6	MP:0008572	abnormal Purkinje cell dendrite morphology	CCO:MP0008572
MGI:1930780	Myh10	"Myh10<tm5Rsad>/Myh10<tm5Rsad>,Tg(CMV-cre)1Cgn/0"	involves: 129S/SvEv * BALB/cJ * C57BL/6	MP:0000875	abnormal cerebellar Purkinje cell layer	CCO:MP0000875
MGI:1930780	Myh10	Myh10<tm5Rsad>/Myh10<tm5Rsad>	involves: 129S/SvEv * C57BL/6	MP:0008572	abnormal Purkinje cell dendrite morphology	CCO:MP0008572
MGI:1930780	Myh10	Myh10<tm4Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1930780	Myh10	Myh10<tm4Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * C57BL/6	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1930780	Myh10	Myh10<tm4Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000828	abnormal fourth ventricle morphology	CCO:MP0000828
MGI:1930780	Myh10	Myh10<tm4Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * C57BL/6	MP:0008535	enlarged lateral ventricles	CCO:MP0008535
MGI:1930780	Myh10	Myh10<tm4Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * C57BL/6	MP:0008536	enlarged third ventricle	CCO:MP0008536
MGI:1930780	Myh10	Myh10<tm5Rsad>/Myh10<tm5Rsad>	involves: 129S/SvEv * C57BL/6	MP:0001405	impaired coordination	CCO:MP0001405
MGI:1930780	Myh10	Myh10<tm4Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * C57BL/6	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:1930780	Myh10	Myh10<tm5Rsad>/Myh10<tm5Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000875	abnormal cerebellar Purkinje cell layer	CCO:MP0000875
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm5Rsad>	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0000828	abnormal fourth ventricle morphology	CCO:MP0000828
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129S/SvEv * C57BL/6	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000828	abnormal fourth ventricle morphology	CCO:MP0000828
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S/SvEv * C57BL/6	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000828	abnormal fourth ventricle morphology	CCO:MP0000828
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm4Rsad>	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0000828	abnormal fourth ventricle morphology	CCO:MP0000828
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm5Rsad>	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1930780	Myh10	Myh10<tm5Rsad>/Myh10<tm5Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000885	ectopic Purkinje cell	CCO:MP0000885
MGI:1930780	Myh10	"Myh10<tm5Rsad>/Myh10<tm5Rsad>,Tg(CMV-cre)1Cgn/0"	involves: 129S/SvEv * BALB/cJ * C57BL/6	MP:0000885	ectopic Purkinje cell	CCO:MP0000885
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0004564	enlarged myocardial fiber	CCO:MP0004564
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0005140	decreased cardiac muscle contractility	CCO:MP0005140
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0002795	dilated cardiomyopathy	CCO:MP0002795
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0001625	cardiac hypertrophy	CCO:MP0001625
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0008788	abnormal fetal cardiomyocyte morphology	CCO:MP0008788
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:1930780	Myh10	Myh10<tm6(Myh9/GFP)Rsad>/Myh10<tm6(Myh9/GFP)Rsad>	involves: 129S/SvEv * C57BL/6	MP:0005608	cardiac interstitial fibrosis	CCO:MP0005608
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0000277	abnormal heart shape	CCO:MP0000277
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0000278	abnormal myocardial fiber morphology	CCO:MP0000278
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0000273	overriding aorta	CCO:MP0000273
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0002747	abnormal aortic valve morphology	CCO:MP0002747
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0001625	cardiac hypertrophy	CCO:MP0001625
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0006138	congestive heart failure	CCO:MP0006138
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0000440	domed skull	CCO:MP0000440
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0004564	enlarged myocardial fiber	CCO:MP0004564
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0001436	abnormal suckling behavior	CCO:MP0001436
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0003956	abnormal body size	CCO:MP0003956
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae * C57BL/6J	MP:0004062	dilated heart right atrium	CCO:MP0004062
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0000872	abnormal external granule cell layer morphology	CCO:MP0000872
MGI:1930780	Myh10	Myh10<tm1Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae	MP:0001625	cardiac hypertrophy	CCO:MP0001625
MGI:1930780	Myh10	Myh10<tm1Rsad>/Myh10<tm1Rsad>	involves: 129S4/SvJae	MP:0001625	cardiac hypertrophy	CCO:MP0001625
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae	MP:0000279	ventricular hypoplasia	CCO:MP0000279
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1930780	Myh10	Myh10<tm2Rsad>/Myh10<tm2Rsad>	involves: 129S4/SvJae	MP:0000955	abnormal spinal cord morphology	CCO:MP0000955
MGI:1930780	Myh10	Myh10<tm3.1Rsad>/Myh10<tm3.1Rsad>	involves: 129S/Sv * BALB/c * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0005294	abnormal heart ventricle morphology	CCO:MP0005294
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0000852	small cerebellum	CCO:MP0000852
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0000849	abnormal cerebellum morphology	CCO:MP0000849
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0001525	impaired balance	CCO:MP0001525
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0001393	ataxia	CCO:MP0001393
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0000889	abnormal cerebellar molecular layer	CCO:MP0000889
MGI:1930780	Myh10	Myh10<tm3Rsad>/Myh10<tm3Rsad>	involves: 129/Sv * C57BL/6	MP:0001071	abnormal facial nerve morphology	CCO:MP0001071
MGI:107717	Myh9	Myh9<Gt(RRE342)Byg>/Myh9<Gt(RRE342)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:107717	Myh9	Myh9<Gt(RRE342)Byg>/Myh9<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:107717	Myh9	"Myh9<tm1.1Gac>/Myh9<tm1.1Gac>,Tg(Pf4-cre)Q3Rsko/0"	involves: 129/Sv * C57BL/6	MP:0005606	increased bleeding time	CCO:MP0005606
MGI:107717	Myh9	"Myh9<tm1.1Gac>/Myh9<tm1.1Gac>,Tg(Pf4-cre)Q3Rsko/0"	involves: 129/Sv * C57BL/6	MP:0005464	abnormal platelet physiology	CCO:MP0005464
MGI:107717	Myh9	"Myh9<tm1.1Gac>/Myh9<tm1.1Gac>,Tg(Pf4-cre)Q3Rsko/0"	involves: 129/Sv * C57BL/6	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:107717	Myh9	"Myh9<tm1.1Gac>/Myh9<tm1.1Gac>,Tg(Pf4-cre)Q3Rsko/0"	involves: 129/Sv * C57BL/6	MP:0003405	abnormal platelet shape	CCO:MP0003405
MGI:107717	Myh9	"Myh9<tm1.1Gac>/Myh9<tm1.1Gac>,Tg(Pf4-cre)Q3Rsko/0"	involves: 129/Sv * C57BL/6	MP:0004720	abnormal platelet morphology	CCO:MP0004720
MGI:107717	Myh9	"Myh9<tm1.1Gac>/Myh9<+>,Tg(Pf4-cre)Q3Rsko/0"	involves: 129/Sv * C57BL/6	MP:0005464	abnormal platelet physiology	CCO:MP0005464
MGI:107717	Myh9	"Myh9<tm1.1Gac>/Myh9<tm1.1Gac>,Tg(Pf4-cre)Q3Rsko/0"	involves: 129/Sv * C57BL/6	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:107717	Myh9	"Myh9<tm1.1Gac>/Myh9<tm1.1Gac>,Tg(Pf4-cre)Q3Rsko/0"	involves: 129/Sv * C57BL/6	MP:0002551	abnormal blood coagulation	CCO:MP0002551
MGI:107717	Myh9	Myh9<tm1Maco>/Myh9<tm1Maco>	involves: 129X1/SvJ	MP:0001685	abnormal endoderm development	CCO:MP0001685
MGI:107717	Myh9	Myh9<Gt(Betageo-btk)1Dash>/Myh9<+>	involves: 129X1/SvJ * C57BL/6	MP:0004765	decreased brainstem auditory evoked potential	CCO:MP0004765
MGI:107717	Myh9	Myh9<Gt(Betageo-btk)1Dash>/Myh9<Gt(Betageo-btk)1Dash>	involves: 129X1/SvJ * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:107717	Myh9	Myh9<Gt(Betageo-btk)1Dash>/Myh9<+>	involves: 129X1/SvJ * C57BL/6	MP:0006325	impaired hearing	CCO:MP0006325
MGI:107717	Myh9	Myh9<tm1Maco>/Myh9<tm1Maco>	involves: 129X1/SvJ	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:107717	Myh9	Myh9<tm1Maco>/Myh9<tm1Maco>	involves: 129X1/SvJ	MP:0001674	abnormal triploblastic development	CCO:MP0001674
MGI:1919200	Nanog	Nanog<tm1Yam>/Nanog<tm1Yam>	involves: 129S4/SvJae	MP:0002583	absent extraembryonic ectoderm	CCO:MP0002583
MGI:1919200	Nanog	Nanog<tm1Yam>/Nanog<tm1Yam>	involves: 129S4/SvJae	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1919200	Nanog	Nanog<tm1Yam>/Nanog<tm1Yam>	involves: 129S4/SvJae	MP:0002582	disorganized extraembryonic tissue	CCO:MP0002582
MGI:1919200	Nanog	Nanog<tm1Yam>/Nanog<tm1Yam>	involves: 129S4/SvJae	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1355328	Nasp	Nasp<tm1Mgor>/Nasp<tm1Mgor>	involves: 129S/SvEv * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1355328	Nasp	Nasp<tm1Mgor>/Nasp<tm1Mgor>	involves: 129S/SvEv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1355328	Nasp	Nasp<tm1Mgor>/Nasp<tm1Mgor>	involves: 129S/SvEv * C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1351625	Nbn	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Nbn<tm1Jpt>/Nbn<tm1Jpt>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0000913	abnormal brain development	CCO:MP0000913
MGI:1351625	Nbn	"Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * 129/Sv	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:1351625	Nbn	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Nbn<tm1Jpt>/Nbn<tm1Jpt>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:1351625	Nbn	"Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * 129/Sv	MP:0001577	anemia	CCO:MP0001577
MGI:1351625	Nbn	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>"	involves: 129 * 129/Sv	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1351625	Nbn	Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>	involves: 129/Sv	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1351625	Nbn	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Nbn<tm1Jpt>/Nbn<tm1Jpt>,Tg(Nes-cre)1Kln/0"	involves: 129S1/SvImJ * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0000433	microcephaly	CCO:MP0000433
MGI:1351625	Nbn	"Atm<tm1Awb>/Atm<tm1Awb>,Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>"	involves: 129S6/SvEvTac * 129/Sv	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1351625	Nbn	"Nbn<tm2.1Jpt>/Nbn<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * 129/Sv	MP:0001577	anemia	CCO:MP0001577
MGI:1351625	Nbn	"Nbn<tm2.1Jpt>/Nbn<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * 129/Sv	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:1351625	Nbn	Nbn<tm3Jpt>/Nbn<tm3Jpt>	involves: 129/Sv	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1351625	Nbn	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Nbn<tm1Jpt>/Nbn<tm1Jpt>"	involves: 129 * 129S7/SvEvBrd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1351625	Nbn	Nbn<tm1Nus>/Nbn<tm1Nus>	involves: 129 * C57BL/6	MP:0005030	absent amnion	CCO:MP0005030
MGI:1351625	Nbn	Nbn<tm1Nus>/Nbn<tm1Nus>	involves: 129 * C57BL/6	MP:0002583	absent extraembryonic ectoderm	CCO:MP0002583
MGI:1351625	Nbn	Nbn<tm1Nus>/Nbn<tm1Nus>	involves: 129 * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0001926	female infertility	CCO:MP0001926
MGI:1351625	Nbn	Nbn<tm1Nus>/Nbn<tm1Nus>	involves: 129 * C57BL/6	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0001658	increased mortality induced by gamma-irradiation	CCO:MP0001658
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<tm1Zqw>	involves: 129S2/SvPas * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0002421	abnormal cell-mediated immunity	CCO:MP0002421
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0003496	thyroid adenoma	CCO:MP0003496
MGI:1351625	Nbn	Nbn<tm1Nus>/Nbn<tm1Nus>	involves: 129 * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1351625	Nbn	Nbn<tm1Nus>/Nbn<tm1Nus>	involves: 129 * C57BL/6	MP:0003988	disorganized embryonic tissue	CCO:MP0003988
MGI:1351625	Nbn	Nbn<tm1Nus>/Nbn<tm1Nus>	involves: 129 * C57BL/6	MP:0004965	inner cell mass degeneration	CCO:MP0004965
MGI:1351625	Nbn	Nbn<tm1Nus>/Nbn<tm1Nus>	involves: 129 * C57BL/6	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0008211	decreased mature B cell number	CCO:MP0008211
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:1351625	Nbn	Nbn<tm1Xu>/Nbn<tm1Xu>	Not Specified	MP:0004805	absent oocytes	CCO:MP0004805
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0009592	Leydig cell tumor	CCO:MP0009592
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0009591	liver adenocarcinoma	CCO:MP0009591
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0009590	gonad tumor	CCO:MP0009590
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<tm1Zqw>	involves: 129S2/SvPas * C57BL/6	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<tm1Zqw>	involves: 129S2/SvPas * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0003324	liver adenoma	CCO:MP0003324
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0001658	increased mortality induced by gamma-irradiation	CCO:MP0001658
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<tm1Zqw>	involves: 129S2/SvPas * C57BL/6	MP:0004965	inner cell mass degeneration	CCO:MP0004965
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<tm1Zqw>	involves: 129S2/SvPas * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1351625	Nbn	Nbn<tm1Zqw>/Nbn<+>	involves: 129S2/SvPas * C57BL/6	MP:0009219	prostate intraepithelial neoplasia	CCO:MP0009219
MGI:1351625	Nbn	Nbn<tm1.1Md>/Nbn<tm1.1Md>	involves: 129/Sv * 129P2/OlaHsd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1351625	Nbn	"Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(CD19-cre/ERT2)1Cgn/0"	Not Specified	MP:0001805	decreased IgG level	CCO:MP0001805
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<+>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:1351625	Nbn	"Nbn<tm1Md>/Nbn<tm1Zqw>,Tg(Mx1-cre)1Cgn/0"	involves: 129/Sv * 129P2/OlaHsd	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1351625	Nbn	"Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(CD19-cre/ERT2)1Cgn/0"	Not Specified	MP:0008497	decreased IgG2b level	CCO:MP0008497
MGI:1351625	Nbn	"Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(CD19-cre/ERT2)1Cgn/0"	Not Specified	MP:0008496	decreased IgG2a level	CCO:MP0008496
MGI:1351625	Nbn	"Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(CD19-cre/ERT2)1Cgn/0"	Not Specified	MP:0005093	decreased B cell proliferation	CCO:MP0005093
MGI:1351625	Nbn	"Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(CD19-cre/ERT2)1Cgn/0"	Not Specified	MP:0002459	abnormal B cell physiology	CCO:MP0002459
MGI:1351625	Nbn	"Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(CD19-cre/ERT2)1Cgn/0"	Not Specified	MP:0008498	decreased IgG3 level	CCO:MP0008498
MGI:1351625	Nbn	"Nbn<tm1Nus>/Nbn<tm2Nus>,Tg(CD19-cre/ERT2)1Cgn/0"	Not Specified	MP:0008495	decreased IgG1 level	CCO:MP0008495
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1351625	Nbn	"Atm<tm1Awb>/Atm<tm1Awb>,Nbn<tm1Jpt>/Nbn<tm1Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<+>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000875	abnormal cerebellar Purkinje cell layer	CCO:MP0000875
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000853	absent cerebellar foliation	CCO:MP0000853
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002690	akinesia	CCO:MP0002690
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0003492	abnormal involuntary movement	CCO:MP0003492
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000745	tremors	CCO:MP0000745
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001393	ataxia	CCO:MP0001393
MGI:1351625	Nbn	"Nbn<tm1Jpt>/Nbn<tm1Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002627	teratoma	CCO:MP0002627
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001525	impaired balance	CCO:MP0001525
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000852	small cerebellum	CCO:MP0000852
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001409	increased stereotypic behavior	CCO:MP0001409
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002182	abnormal astrocyte morphology	CCO:MP0002182
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000872	abnormal external granule cell layer morphology	CCO:MP0000872
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000875	abnormal cerebellar Purkinje cell layer	CCO:MP0000875
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000853	absent cerebellar foliation	CCO:MP0000853
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000852	small cerebellum	CCO:MP0000852
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002690	akinesia	CCO:MP0002690
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0003492	abnormal involuntary movement	CCO:MP0003492
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<+>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0001525	impaired balance	CCO:MP0001525
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001406	abnormal gait	CCO:MP0001406
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002182	abnormal astrocyte morphology	CCO:MP0002182
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000745	tremors	CCO:MP0000745
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001406	abnormal gait	CCO:MP0001406
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002022	lymphoma	CCO:MP0002022
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001525	impaired balance	CCO:MP0001525
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001409	increased stereotypic behavior	CCO:MP0001409
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0001393	ataxia	CCO:MP0001393
MGI:1351625	Nbn	Nbn<tm1Jpt>/Nbn<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:1351625	Nbn	"Nbn<tm1Jpt>/Nbn<tm1Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002032	sarcoma	CCO:MP0002032
MGI:1351625	Nbn	"Nbn<tm1Jpt>/Nbn<tm1Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002022	lymphoma	CCO:MP0002022
MGI:1351625	Nbn	Nbn<tm1Jpt>/Nbn<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1351625	Nbn	Nbn<tm1Jpt>/Nbn<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1351625	Nbn	"Nbn<tm1Jpt>/Nbn<tm1Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:1351625	Nbn	"Nbn<tm2Zqw>/Nbn<tm2.1Zqw>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000872	abnormal external granule cell layer morphology	CCO:MP0000872
MGI:1923294	Ncapg2	Ncapg2<tm1Jdc>/Ncapg2<tm1Jdc>	involves: 129S1/Sv * C57BL/6	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:1923294	Ncapg2	Ncapg2<tm1Jdc>/Ncapg2<tm1Jdc>	involves: 129S1/Sv * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1923294	Ncapg2	Ncapg2<tm1Jdc>/Ncapg2<tm1Jdc>	involves: 129S1/Sv * C57BL/6	MP:0001694	failure to form egg cylinders	CCO:MP0001694
MGI:1914453	Nde1	Nde1<tm1Caw>/Nde1<tm1Caw>	involves: 129S4/SvJae * Black Swiss	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:1914453	Nde1	Nde1<tm1Caw>/Nde1<tm1Caw>	involves: 129S4/SvJae * Black Swiss	MP:0002175	decreased brain weight	CCO:MP0002175
MGI:1914453	Nde1	Nde1<tm1Caw>/Nde1<tm1Caw>	involves: 129S4/SvJae * Black Swiss	MP:0000774	decreased brain size	CCO:MP0000774
MGI:1914453	Nde1	Nde1<tm1Caw>/Nde1<tm1Caw>	involves: 129S4/SvJae * Black Swiss	MP:0003241	loss of cortex neurons	CCO:MP0003241
MGI:1914453	Nde1	Nde1<tm1Caw>/Nde1<tm1Caw>	involves: 129S4/SvJae * Black Swiss	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:1914453	Nde1	Nde1<tm1Caw>/Nde1<tm1Caw>	involves: 129S4/SvJae * Black Swiss	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0008173	increased follicular B cell number	CCO:MP0008173
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0008182	decreased marginal zone B cell number	CCO:MP0008182
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0008101	lymph node hypoplasia	CCO:MP0008101
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0003156	abnormal leukocyte migration/homing	CCO:MP0003156
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0002458	abnormal B cell number	CCO:MP0002458
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0000694	spleen hypoplasia	CCO:MP0000694
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0002444	abnormal T cell physiology	CCO:MP0002444
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:97302	Nedd9	Nedd9<tm1Miku>/Nedd9<tm1Miku>	B6.CB-Nedd9<tm1Miku>	MP:0008191	abnormal follicular B cell physiology	CCO:MP0008191
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0005537	abnormal cerebral aqueduct	CCO:MP0005537
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0002200	abnormal brain ventricle/choroid plexus morphology	CCO:MP0002200
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000829	dilated fourth ventricle	CCO:MP0000829
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000825	dilated lateral ventricles	CCO:MP0000825
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000827	dilated third ventricle	CCO:MP0000827
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000825	dilated lateral ventricles	CCO:MP0000825
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000820	abnormal choroid plexus morphology	CCO:MP0000820
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0002200	abnormal brain ventricle/choroid plexus morphology	CCO:MP0002200
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0002741	small olfactory bulb	CCO:MP0002741
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000827	dilated third ventricle	CCO:MP0000827
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0002741	small olfactory bulb	CCO:MP0002741
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000445	short snout	CCO:MP0000445
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	B6.RBF(C3Fe)-Nek1<kat>/J	MP:0000440	domed skull	CCO:MP0000440
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000917	obstructive hydrocephaly	CCO:MP0000917
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000522	kidney cortex cysts	CCO:MP0000522
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * RBF/Dn	MP:0001265	decreased body size	CCO:MP0001265
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000435	shortened head	CCO:MP0000435
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0002083	premature death	CCO:MP0002083
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0001265	decreased body size	CCO:MP0001265
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000917	obstructive hydrocephaly	CCO:MP0000917
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * RBF/Dn	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * RBF/Dn	MP:0001925	male infertility	CCO:MP0001925
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000819	abnormal olfactory bulb morphology	CCO:MP0000819
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * RBF/Dn	MP:0002083	premature death	CCO:MP0002083
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0001577	anemia	CCO:MP0001577
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000820	abnormal choroid plexus morphology	CCO:MP0000820
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000819	abnormal olfactory bulb morphology	CCO:MP0000819
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	RBF/Dn	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	RBF/Dn	MP:0000416	sparse hair	CCO:MP0000416
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	RBF/Dn	MP:0001258	decreased body length	CCO:MP0001258
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0000829	dilated fourth ventricle	CCO:MP0000829
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000522	kidney cortex cysts	CCO:MP0000522
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * RBF/Dn	MP:0001258	decreased body length	CCO:MP0001258
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0001147	small testis	CCO:MP0001147
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	B6.RBF(C3Fe)-Nek1<kat>/J	MP:0001265	decreased body size	CCO:MP0001265
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	B6.RBF(C3Fe)-Nek1<kat>/J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0001258	decreased body length	CCO:MP0001258
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0001265	decreased body size	CCO:MP0001265
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0001925	male infertility	CCO:MP0001925
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	RBF/Dn	MP:0000440	domed skull	CCO:MP0000440
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0001940	testicular hypoplasia	CCO:MP0001940
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0001577	anemia	CCO:MP0001577
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	B6.RBF(C3Fe)-Nek1<kat>/J	MP:0008974	proportional dwarf	CCO:MP0008974
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000445	short snout	CCO:MP0000445
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0001258	decreased body length	CCO:MP0001258
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0000435	shortened head	CCO:MP0000435
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0002083	premature death	CCO:MP0002083
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0005537	abnormal cerebral aqueduct	CCO:MP0005537
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0002703	abnormal renal tubule morphology	CCO:MP0002703
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97303	Nek1	Nek1<kat-2J>/Nek1<kat-2J>	C57BL/6J-Nek1<kat-2J>/J	MP:0002643	poikilocytosis	CCO:MP0002643
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	RBF/Dn	MP:0002083	premature death	CCO:MP0002083
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	RBF/Dn	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	RBF/Dn	MP:0001265	decreased body size	CCO:MP0001265
MGI:97303	Nek1	Nek1<kat>/Nek1<kat>	involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn	MP:0003657	abnormal erythrocyte lysis	CCO:MP0003657
MGI:107754	Neurog1	"Neurog1<tm1And>/Neurog1<tm1And>,Neurog2<tm2Fgu>/Neurog2<tm2Fgu>"	involves: 129/Sv * C57BL/6J * CD-1	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:107754	Neurog1	"Neurog1<tm1And>/Neurog1<tm1And>,Neurog2<tm2Fgu>/Neurog2<tm2Fgu>"	involves: 129/Sv * C57BL/6J * CD-1	MP:0000832	abnormal thalamus morphology	CCO:MP0000832
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001101	abnormal superior vagus ganglion morphology	CCO:MP0001101
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001056	abnormal cranial nerve morphology	CCO:MP0001056
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001092	abnormal trigeminal ganglion morphology	CCO:MP0001092
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001081	abnormal cranial ganglia morphology	CCO:MP0001081
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001075	abnormal accessory nerve morphology	CCO:MP0001075
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001065	abnormal trigeminal nerve morphology	CCO:MP0001065
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001097	abnormal superior glossopharyngeal ganglion morphology	CCO:MP0001097
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:107754	Neurog1	Neurog1<tm1And>/Neurog1<tm1And>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001436	abnormal suckling behavior	CCO:MP0001436
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0000286	abnormal mitral valve morphology	CCO:MP0000286
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0006113	abnormal heart septum morphology	CCO:MP0006113
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0001625	cardiac hypertrophy	CCO:MP0001625
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0002624	abnormal tricuspid valve morphology	CCO:MP0002624
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:102469	Nfatc1	Nfatc1<tm1Mak>/Nfatc1<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6	MP:0002746	abnormal semilunar valve morphology	CCO:MP0002746
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0004830	short incisors	CCO:MP0004830
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0004791	absent lower incisors	CCO:MP0004791
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0002764	short tibia	CCO:MP0002764
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0004831	long incisors	CCO:MP0004831
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0000067	osteopetrosis	CCO:MP0000067
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0008272	abnormal endochondral bone ossification	CCO:MP0008272
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Sh3bp2<tm1Bjro>/Sh3bp2<tm1Bjro>,Tg(Mx1-cre)1Cgn/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0008396	abnormal osteoclast differentiation	CCO:MP0008396
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Sh3bp2<tm1Bjro>/Sh3bp2<tm1Bjro>,Tg(Mx1-cre)1Cgn/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0004985	decreased osteoclast cell number	CCO:MP0004985
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0008396	abnormal osteoclast differentiation	CCO:MP0008396
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0004985	decreased osteoclast cell number	CCO:MP0004985
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0004686	decreased length of long bones	CCO:MP0004686
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0004595	abnormal mandibular condyloid process morphology	CCO:MP0004595
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Sh3bp2<tm1Bjro>/Sh3bp2<tm1Bjro>,Tg(Mx1-cre)1Cgn/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0003865	lymph node inflammation	CCO:MP0003865
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Sh3bp2<tm1Bjro>/Sh3bp2<tm1Bjro>,Tg(Mx1-cre)1Cgn/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001873	stomach inflammation	CCO:MP0001873
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0003408	increased width of hypertrophic chondrocyte zone	CCO:MP0003408
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0003109	short femur	CCO:MP0003109
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Sh3bp2<tm1Bjro>/Sh3bp2<tm1Bjro>,Tg(Mx1-cre)1Cgn/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001860	liver inflammation	CCO:MP0001860
MGI:102469	Nfatc1	"Nfatc1<tm3Glm>/Nfatc1<tm3Glm>,Sh3bp2<tm1Bjro>/Sh3bp2<tm1Bjro>,Tg(Mx1-cre)1Cgn/0"	involves: 129S4/SvJae * C57BL/6 * CBA	MP:0001861	lung inflammation	CCO:MP0001861
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0001790	abnormal immune system physiology	CCO:MP0001790
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0008500	increased IgG2a level	CCO:MP0008500
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0008559	abnormal interferon-gamma secretion	CCO:MP0008559
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0008686	abnormal interleukin-2 secretion	CCO:MP0008686
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0008700	decreased interleukin-4 secretion	CCO:MP0008700
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0001544	abnormal cardiovascular system physiology	CCO:MP0001544
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0008498	decreased IgG3 level	CCO:MP0008498
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0002128	abnormal blood circulation	CCO:MP0002128
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0002746	abnormal semilunar valve morphology	CCO:MP0002746
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0002747	abnormal aortic valve morphology	CCO:MP0002747
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0002748	abnormal pulmonary valve morphology	CCO:MP0002748
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0006049	semilunar valve regurgitation	CCO:MP0006049
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0003717	pallor	CCO:MP0003717
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002723	abnormal immune serum protein physiology	CCO:MP0002723
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0001785	edema	CCO:MP0001785
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002444	abnormal T cell physiology	CCO:MP0002444
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002495	increased IgA level	CCO:MP0002495
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002501	abnormal inflammatory mediator physiology	CCO:MP0002501
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002492	decreased IgE level	CCO:MP0002492
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0005016	decreased lymphocyte cell number	CCO:MP0005016
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0008497	decreased IgG2b level	CCO:MP0008497
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm1Glm>	involves: 129S2/SvPas	MP:0000465	gastrointestinal hemorrhage	CCO:MP0000465
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002494	increased IgM level	CCO:MP0002494
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002459	abnormal B cell physiology	CCO:MP0002459
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002490	abnormal immunoglobulin level	CCO:MP0002490
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002461	increased immunoglobulin level	CCO:MP0002461
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0002460	decreased immunoglobulin level	CCO:MP0002460
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0005466	abnormal T-helper 2 physiology	CCO:MP0005466
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0003945	abnormal lymphocyte physiology	CCO:MP0003945
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0008495	decreased IgG1 level	CCO:MP0008495
MGI:102469	Nfatc1	Nfatc1<tm1Glm>/Nfatc1<tm2Glm>	chimera involves: 129S2/SvPas	MP:0000717	abnormal lymphocyte cell number	CCO:MP0000717
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0001293	anophthalmia	CCO:MP0001293
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003232	abnormal forebrain development	CCO:MP0003232
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003396	abnormal embryonic hematopoiesis	CCO:MP0003396
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:106184	Npm1	"Npm1<tm1Ppp>/Npm1<+>,Tg(IghMyc)22Bri/0"	involves: 129S1/Sv * C57BL/6 * SJL	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:106184	Npm1	Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:106184	Npm1	Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>	involves: 129P2/OlaHsd * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:106184	Npm1	Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>	involves: 129P2/OlaHsd * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:106184	Npm1	Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>	involves: 129P2/OlaHsd * C57BL/6	MP:0001712	abnormal placenta development	CCO:MP0001712
MGI:106184	Npm1	Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>	involves: 129P2/OlaHsd * C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:106184	Npm1	"Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:106184	Npm1	"Npm1<tm1Ppp>/Npm1<+>,Tg(IghMyc)22Bri/0"	involves: 129S1/Sv * C57BL/6 * SJL	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:106184	Npm1	"Npm1<tm1Ppp>/Npm1<tm1Ppp>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:106184	Npm1	"Npm1<tm1Ppp>/Npm1<tm1Ppp>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:106184	Npm1	"Npm1<tm1Ppp>/Npm1<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003396	abnormal embryonic hematopoiesis	CCO:MP0003396
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003232	abnormal forebrain development	CCO:MP0003232
MGI:106184	Npm1	"Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0002417	abnormal megakaryocyte morphology	CCO:MP0002417
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:106184	Npm1	Npm1<Gt(OST331547)Lex>/Npm1<Gt(OST331547)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:106184	Npm1	"Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:106184	Npm1	Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>	involves: 129P2/OlaHsd * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0002590	increased mean corpuscular volume	CCO:MP0002590
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0002642	anisocytosis	CCO:MP0002642
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0002416	abnormal proerythroblast morphology	CCO:MP0002416
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0000228	abnormal thrombopoiesis	CCO:MP0000228
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0002424	abnormal reticulocyte morphology	CCO:MP0002424
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0004259	small placenta	CCO:MP0004259
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<tm1Ppp>	involves: 129S1/Sv * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:106184	Npm1	Npm1<tm1Ppp>/Npm1<+>	involves: 129S1/Sv * C57BL/6	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:106184	Npm1	Npm1<tm2Ppp>/Npm1<tm2Ppp>	involves: 129S1/Sv * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:97376	Nras	"Nras<tm1Tyj>/Nras<+>,Tg(Vil-cre)20Syr/0"	involves: C57BL/6 * DBA/2	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:97376	Nras	"Hras1<tm1Esn>/Hras1<tm1Esn>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * C57BL/6N	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:97376	Nras	Nras<tm1Rak>/Nras<tm1Rak>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<tm1Tyj>,Nras<tm1Rak>/Nras<+>"	involves: 129/Sv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0000592	short tail	CCO:MP0000592
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<tm1Tyj>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0001721	absent blood islands	CCO:MP0001721
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0004937	dilated heart	CCO:MP0004937
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0003396	abnormal embryonic hematopoiesis	CCO:MP0003396
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:97376	Nras	"Kras<tm1Tyj>/Kras<+>,Nras<tm1Rak>/Nras<tm1Rak>"	involves: 129/Sv * C57BL/6	MP:0000292	distended pericardial sacs	CCO:MP0000292
MGI:1095411	Nup214	Nup214<tm1Gcg>/Nup214<tm1Gcg>	involves: 129P2/OlaHsd	MP:0004963	abnormal blastocoele morphology	CCO:MP0004963
MGI:1095411	Nup214	Nup214<tm1Gcg>/Nup214<tm1Gcg>	involves: 129P2/OlaHsd	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:104749	Osm	Osm<tm1Ymo>/Osm<tm1Ymo>	B6J.Cg-Osm<tm1Ymo>	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:104749	Osm	Osm<tm1Ymo>/Osm<tm1Ymo>	B6J.Cg-Osm<tm1Ymo>	MP:0003043	hypoalgesia	CCO:MP0003043
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	B6.129-Ovol1<tm1Efu>	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	B6.129-Ovol1<tm1Efu>	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	B6.129-Ovol1<tm1Efu>	MP:0002796	impaired skin barrier function	CCO:MP0002796
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	B6.129-Ovol1<tm1Efu>	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<+>	B6.129-Ovol1<tm1Efu>	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004970	kidney atrophy	CCO:MP0004970
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001136	dilated cervix	CCO:MP0001136
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000522	kidney cortex cysts	CCO:MP0000522
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003809	abnormal hair shaft morphology	CCO:MP0003809
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001144	vagina atresia	CCO:MP0001144
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001143	constricted vagina opening	CCO:MP0001143
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001123	dilated uterus	CCO:MP0001123
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000400	abnormal awl hair	CCO:MP0000400
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000395	abnormal hair types	CCO:MP0000395
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000405	abnormal auchene hairs	CCO:MP0000405
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000420	ruffled hair	CCO:MP0000420
MGI:1330290	Ovol1	Ovol1<tm1Efu>/Ovol1<tm1Efu>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000398	splitting of guard hairs	CCO:MP0000398
MGI:109520	Pafah1b1	"Lrp8<tm1Her>/Lrp8<tm1Her>,Pafah1b1<tm1Awb>/Pafah1b1<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000788	abnormal cerebral cortex morphology	CCO:MP0000788
MGI:109520	Pafah1b1	"Lrp8<tm1Her>/Lrp8<tm1Her>,Pafah1b1<tm1Awb>/Pafah1b1<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000813	abnormal hippocampal laminar structure	CCO:MP0000813
MGI:109520	Pafah1b1	Pafah1b1<tm1Or>/Pafah1b1<+>	Not Specified	MP:0003648	abnormal radial glial cell morphology	CCO:MP0003648
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>"	involves: 129S6/SvEvTac	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Ywhae<tm1Awb>/Ywhae<+>"	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Ywhae<tm1Awb>/Ywhae<+>"	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<tm2Awb>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0000790	abnormal stratification in cerebral cortex	CCO:MP0000790
MGI:109520	Pafah1b1	Pafah1b1<tm1Or>/Pafah1b1<+>	Not Specified	MP:0001889	delayed brain development	CCO:MP0001889
MGI:109520	Pafah1b1	Pafah1b1<tm2.2Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000819	abnormal olfactory bulb morphology	CCO:MP0000819
MGI:109520	Pafah1b1	Pafah1b1<tm2.2Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:109520	Pafah1b1	Pafah1b1<tm2.2Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000822	abnormal brain ventricle morphology	CCO:MP0000822
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<tm2Awb>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>"	involves: 129S6/SvEvTac	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<tm2Awb>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0000885	ectopic Purkinje cell	CCO:MP0000885
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0006378	abnormal spermatogonia morphology	CCO:MP0006378
MGI:109520	Pafah1b1	Pafah1b1<tm2.2Awb>/Pafah1b1<tm2.2Awb>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109520	Pafah1b1	Pafah1b1<tm1Or>/Pafah1b1<+>	Not Specified	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<tm2Awb>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0001265	decreased body size	CCO:MP0001265
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Pafah1b2<Gt(Betageo)1Cla>/Pafah1b2<Gt(Betageo)1Cla>,Pafah1b3<tm1Cla>/Pafah1b3<tm1Cla>"	involves: 129S6/SvEvTac	MP:0006304	abnormal seminiferous epithelium morphology	CCO:MP0006304
MGI:109520	Pafah1b1	Pafah1b1<tm2.2Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000790	abnormal stratification in cerebral cortex	CCO:MP0000790
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<tm2Awb>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0000813	abnormal hippocampal laminar structure	CCO:MP0000813
MGI:109520	Pafah1b1	Pafah1b1<tm1Or>/Pafah1b1<tm1Or>	Not Specified	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<tm2Awb>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0000812	abnormal dentate gyrus morphology	CCO:MP0000812
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0005159	azoospermia	CCO:MP0005159
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0008279	arrest of spermiogenesis	CCO:MP0008279
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<tm2Awb>	involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss	MP:0008284	abnormal hippocampus pyramidal cell layer	CCO:MP0008284
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Ywhae<tm1Awb>/Ywhae<+>"	either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0004182	abnormal spermiation	CCO:MP0004182
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0001925	male infertility	CCO:MP0001925
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0001932	abnormal spermiogenesis	CCO:MP0001932
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0001147	small testis	CCO:MP0001147
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0002208	abnormal germ cell morphology	CCO:MP0002208
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:109520	Pafah1b1	Pafah1b1<tm2Awb>/Pafah1b1<tm2Awb>	involves: 129S/SvEv * FVB/N * NIH Black Swiss	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:109520	Pafah1b1	Pafah1b1<Gt(IRESBetageo)1Hha>/Pafah1b1<Gt(IRESBetageo)1Hha>	involves: 129/Sv * NMRI	MP:0008898	abnormal acrosome morphology	CCO:MP0008898
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000819	abnormal olfactory bulb morphology	CCO:MP0000819
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000822	abnormal brain ventricle morphology	CCO:MP0000822
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac	MP:0008284	abnormal hippocampus pyramidal cell layer	CCO:MP0008284
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0001405	impaired coordination	CCO:MP0001405
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0001889	delayed brain development	CCO:MP0001889
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Ndel1<tm1.1Shr>/Ndel1<+>"	involves: 129S6/SvEvTac	MP:0008547	abnormal neocortex morphology	CCO:MP0008547
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0001513	limb grasping	CCO:MP0001513
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Ndel1<tm1.1Shr>/Ndel1<+>"	involves: 129S6/SvEvTac	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Ndel1<tm1.1Shr>/Ndel1<+>"	involves: 129S6/SvEvTac	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:109520	Pafah1b1	"Pafah1b1<tm2.2Awb>/Pafah1b1<+>,Ndel1<tm1.1Shr>/Ndel1<+>"	involves: 129S6/SvEvTac	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:109520	Pafah1b1	"Pafah1b1<tm1Awb>/Pafah1b1<+>,Ndel1<tm1.1Shr>/Ndel1<+>"	involves: 129S6/SvEvTac	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac	MP:0006009	abnormal neuronal migration	CCO:MP0006009
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<tm1Awb>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac	MP:0008547	abnormal neocortex morphology	CCO:MP0008547
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000790	abnormal stratification in cerebral cortex	CCO:MP0000790
MGI:109520	Pafah1b1	Pafah1b1<tm1Awb>/Pafah1b1<+>	involves: 129S6/SvEvTac * NIH Black Swiss	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:109520	Pafah1b1	"Pafah1b1<tm2.2Awb>/Pafah1b1<+>,Ndel1<tm1.1Shr>/Ndel1<+>"	involves: 129S6/SvEvTac	MP:0005442	abnormal pyramidal neuron morphology	CCO:MP0005442
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0001785	edema	CCO:MP0001785
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0000934	abnormal telencephalon development	CCO:MP0000934
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0004055	atrial hypoplasia	CCO:MP0004055
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0000592	short tail	CCO:MP0000592
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0000279	ventricular hypoplasia	CCO:MP0000279
MGI:2135608	Pard3	Pard3<tm1.1Shoh>/Pard3<tm1.1Shoh>	involves: 129S4/SvJae * C57BL/6 * C57BL/6J	MP:0008725	enlarged heart atrium	CCO:MP0008725
MGI:1860764	Pde3a	Pde3a<tm1Vman>/Pde3a<tm1Vman>	either: (involves: 129X1/SvJ * C57BL/6J) or (involves: 129X1/SvJ * Black Swiss * C57BL/6J)	MP:0001926	female infertility	CCO:MP0001926
MGI:1860764	Pde3a	Pde3a<tm1Vman>/Pde3a<tm1Vman>	either: (involves: 129X1/SvJ * C57BL/6J) or (involves: 129X1/SvJ * Black Swiss * C57BL/6J)	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<+>	involves: 129S6/SvEvTac	MP:0004038	lymphangiectasis	CCO:MP0004038
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<+>	involves: 129S6/SvEvTac	MP:0001879	abnormal lymphatic vessel morphology	CCO:MP0001879
MGI:103098	Pdpn	Pdpn<tm1Bwd>/Pdpn<tm1Bwd>	either: (involves: Black Swiss) or (involves: C57BL/6)	MP:0009432	increased fetal weight	CCO:MP0009432
MGI:103098	Pdpn	Pdpn<tm1Bwd>/Pdpn<tm1Bwd>	either: (involves: Black Swiss) or (involves: C57BL/6)	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:103098	Pdpn	Pdpn<tm1Bwd>/Pdpn<tm1Bwd>	either: (involves: Black Swiss) or (involves: C57BL/6)	MP:0001953	respiratory failure	CCO:MP0001953
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0003057	abnormal epicardium morphology	CCO:MP0003057
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0002189	abnormal myocardial trabeculae morphology	CCO:MP0002189
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0000272	abnormal aorta morphology	CCO:MP0000272
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0000301	decreased endocardial cushion size	CCO:MP0000301
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0000486	abnormal pulmonary trunk morphology	CCO:MP0000486
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0004111	abnormal coronary artery morphology	CCO:MP0004111
MGI:103098	Pdpn	Pdpn<tm1Acgg>/Pdpn<tm1Acgg>	involves: 129S1/Sv * 129X1/SvJ * Swiss	MP:0005329	abnormal cardiac muscle morphology	CCO:MP0005329
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0004197	abnormal fetal growth/weight/body size	CCO:MP0004197
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0002274	abnormal type I pneumocyte morphology	CCO:MP0002274
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0004038	lymphangiectasis	CCO:MP0004038
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0001953	respiratory failure	CCO:MP0001953
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0005202	lethargy	CCO:MP0005202
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0003390	lymphedema	CCO:MP0003390
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0003659	abnormal lymph circulation	CCO:MP0003659
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0001575	cyanosis	CCO:MP0001575
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0001179	thick alveolar septum	CCO:MP0001179
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0002270	abnormal respiratory alveoli morphology	CCO:MP0002270
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0001879	abnormal lymphatic vessel morphology	CCO:MP0001879
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0002096	abnormal skin condition/ morphology	CCO:MP0002096
MGI:103098	Pdpn	Pdpn<tm1Mcws>/Pdpn<tm1Mcws>	involves: 129S6/SvEvTac	MP:0001177	atelectasis	CCO:MP0001177
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0004620	cervical vertebral fusion	CCO:MP0004620
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0004607	abnormal cervical atlas morphology	CCO:MP0004607
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<+>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0004505	decreased renal glomerulus number	CCO:MP0004505
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0003604	single kidney	CCO:MP0003604
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0003446	renal hypoplasia	CCO:MP0003446
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0006107	abnormal atrioventricular canal morphology	CCO:MP0006107
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000157	abnormal sternum morphology	CCO:MP0000157
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0004615	cervical vertebral transformation	CCO:MP0004615
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006107	abnormal atrioventricular canal morphology	CCO:MP0006107
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003140	dilated atria	CCO:MP0003140
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003078	aphakia	CCO:MP0003078
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001044	abnormal enteric nervous system morphology	CCO:MP0001044
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0009703	decreased birth body size	CCO:MP0009703
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000297	abnormal endocardial cushion morphology	CCO:MP0000297
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0008148	abnormal rib-sternum attachment	CCO:MP0008148
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001306	small lens	CCO:MP0001306
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<+>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<+>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0009674	decreased birth weight	CCO:MP0009674
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001306	small lens	CCO:MP0001306
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003425	abnormal optic vesicle formation	CCO:MP0003425
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003140	dilated atria	CCO:MP0003140
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000297	abnormal endocardial cushion morphology	CCO:MP0000297
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006107	abnormal atrioventricular canal morphology	CCO:MP0006107
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1918771	Pds5a	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001044	abnormal enteric nervous system morphology	CCO:MP0001044
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0001044	abnormal enteric nervous system morphology	CCO:MP0001044
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000520	absent kidney	CCO:MP0000520
MGI:1918771	Pds5a	Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000547	short limbs	CCO:MP0000547
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003755	abnormal palate morphology	CCO:MP0003755
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002116	abnormal craniofacial bone morphology	CCO:MP0002116
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003775	thin lip	CCO:MP0003775
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006107	abnormal atrioventricular canal morphology	CCO:MP0006107
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003345	decreased rib number	CCO:MP0003345
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003056	abnormal hyoid bone morphology	CCO:MP0003056
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004351	short humerus	CCO:MP0004351
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002209	decreased germ cell number	CCO:MP0002209
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003723	abnormal long bone morphology	CCO:MP0003723
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001255	decreased body height	CCO:MP0001255
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003743	abnormal facial morphology	CCO:MP0003743
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000433	microcephaly	CCO:MP0000433
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005225	abnormal vertebrae development	CCO:MP0005225
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004201	fetal growth retardation	CCO:MP0004201
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004321	short sternum	CCO:MP0004321
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004340	short scapula	CCO:MP0004340
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000154	rib fusion	CCO:MP0000154
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000445	short snout	CCO:MP0000445
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000088	short mandible	CCO:MP0000088
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008312	abnormal sympathetic postganglionic fiber	CCO:MP0008312
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001011	abnormal superior cervical ganglion morphology	CCO:MP0001011
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001044	abnormal enteric nervous system morphology	CCO:MP0001044
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004537	abnormal palatine shelf	CCO:MP0004537
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004359	short ulna	CCO:MP0004359
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001575	cyanosis	CCO:MP0001575
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004355	short radius	CCO:MP0004355
MGI:2140945	Pds5b	Pds5b<tm1Jmi>/Pds5b<tm1Jmi>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008277	abnormal sternum ossification	CCO:MP0008277
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003140	dilated atria	CCO:MP0003140
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001306	small lens	CCO:MP0001306
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006107	abnormal atrioventricular canal morphology	CCO:MP0006107
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000297	abnormal endocardial cushion morphology	CCO:MP0000297
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003425	abnormal optic vesicle formation	CCO:MP0003425
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001044	abnormal enteric nervous system morphology	CCO:MP0001044
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002633	persistent truncus arteriosis	CCO:MP0002633
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003078	aphakia	CCO:MP0003078
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006107	abnormal atrioventricular canal morphology	CCO:MP0006107
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001044	abnormal enteric nervous system morphology	CCO:MP0001044
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001306	small lens	CCO:MP0001306
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000297	abnormal endocardial cushion morphology	CCO:MP0000297
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<+>,Pds5b<tm1Jmi>/Pds5b<tm1Jmi>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003140	dilated atria	CCO:MP0003140
MGI:2140945	Pds5b	"Pds5a<Gt(RRM243)Byg>/Pds5a<Gt(RRM243)Byg>,Pds5b<tm1Jmi>/Pds5b<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0002836	abnormal chorion morphology	CCO:MP0002836
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0004025	polyploidy	CCO:MP0004025
MGI:2145154	Pelo	Pelo<tm1Imad>/Pelo<tm1Imad>	either: 129/Sv or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)	MP:0004024	aneuploidy	CCO:MP0004024
MGI:1890613	Pes1	Pes1<tm1Sad>/Pes1<tm1Sad>	involves: 129S1/Sv * 129X1/SvJ	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1890613	Pes1	Pes1<tm1Sad>/Pes1<tm1Sad>	involves: 129S1/Sv * 129X1/SvJ	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1890613	Pes1	Pes1<tm1Sad>/Pes1<tm1Sad>	involves: 129S1/Sv * 129X1/SvJ	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0000914	exencephaly	CCO:MP0000914
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0000774	decreased brain size	CCO:MP0000774
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0000784	forebrain hypoplasia	CCO:MP0000784
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0000850	absent cerebellum	CCO:MP0000850
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0000571	interdigital webbing	CCO:MP0000571
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0003451	absent olfactory bulb	CCO:MP0003451
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0000786	abnormal embryonic neuroepithelial layer differentiation	CCO:MP0000786
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0003861	abnormal nervous system development	CCO:MP0003861
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0004274	abnormal embryonic/fetal subventricular zone morphology	CCO:MP0004274
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0008535	enlarged lateral ventricles	CCO:MP0008535
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0000913	abnormal brain development	CCO:MP0000913
MGI:1355330	Phgdh	Phgdh<tm1.1Shfu>/Phgdh<tm1.1Shfu>	involves: 129P2/OlaHsd * C57BL/6J * FVB/N	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	MP:0008392	decreased primordial germ cell number	CCO:MP0008392
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	MP:0008871	abnormal ovarian follicle number	CCO:MP0008871
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	MP:0001326	retinal degeneration	CCO:MP0001326
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	involves: 129P2/OlaHsd * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	MP:0008390	abnormal primordial germ cell proliferation	CCO:MP0008390
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1346036	Pin1	Pin1<tm1Tuc>/Pin1<tm1Tuc>	B6.129P2-Pin1<tm1Tuc>	MP:0001935	decreased litter size	CCO:MP0001935
MGI:1928897	Piwil1	Piwil1<tm1Hfl>/Piwil1<tm1Hfl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1928897	Piwil1	Piwil1<tm1Hfl>/Piwil1<tm1Hfl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0006362	abnormal male germ cell morphology	CCO:MP0006362
MGI:1928897	Piwil1	Piwil1<tm1Hfl>/Piwil1<tm1Hfl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1928897	Piwil1	Piwil1<tm1Hfl>/Piwil1<tm1Hfl>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:1930036	Piwil2	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1930036	Piwil2	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1930036	Piwil2	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:1930036	Piwil2	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:1930036	Piwil2	Piwil2<tm1Nkn>/Piwil2<tm1Nkn>	involves: 129S2/SvPas * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:3041167	Piwil4	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:3041167	Piwil4	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:3041167	Piwil4	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:3041167	Piwil4	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:3041167	Piwil4	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:3041167	Piwil4	Piwil4<tm1Ghan>/Piwil4<tm1Ghan>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:97603	Pkd1	Pkd1<tm1Maa>/Pkd1<tm1Maa>	involves: 129S4/SvJae * C57BL/6	MP:0001786	skin edema	CCO:MP0001786
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0004860	dilated kidney collecting duct	CCO:MP0004860
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0004755	abnormal loop of Henle	CCO:MP0004755
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0003327	liver cysts	CCO:MP0003327
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0003068	enlarged kidney	CCO:MP0003068
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0003045	fibrosis	CCO:MP0003045
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:97603	Pkd1	Pkd1<tm1Maa>/Pkd1<tm1Maa>	involves: 129S4/SvJae * C57BL/6	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:97603	Pkd1	Pkd1<tm1Maa>/Pkd1<tm1Maa>	involves: 129S4/SvJae * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:97603	Pkd1	Pkd1<tm1Maa>/Pkd1<tm1Maa>	involves: 129S4/SvJae * C57BL/6	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm1Maa>/Pkd1<tm1Maa>	involves: 129S4/SvJae * C57BL/6	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Maa>/Pkd1<tm1Maa>	involves: 129S4/SvJae * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97603	Pkd1	Pkd1<tm1Maa>/Pkd1<tm1Maa>	involves: 129S4/SvJae * C57BL/6	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:97603	Pkd1	"Pkd1<tm1Ggg>/Pkd1<+>,Pkhd1<tm1.1Ggg>/Pkhd1<tm1.1Ggg>"	involves: 129S/SvEv * 129S4/SvJae * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Ggt1-cre)1Egn/0"	involves: 129P2/OlaHsd * C57BL/6 * SJL	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97603	Pkd1	Pkd1<tm3.1Jzh>/Pkd1<tm3.1Jzh>	involves: 129P2/OlaHsd * C57BL/6	MP:0004020	polyhydramnios	CCO:MP0004020
MGI:97603	Pkd1	Pkd1<tm3.1Jzh>/Pkd1<tm3.1Jzh>	involves: 129P2/OlaHsd * C57BL/6	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	involves: 129S4/SvJae * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	involves: 129S4/SvJae * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	involves: 129S4/SvJae * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	involves: 129S4/SvJae * C57BL/6	MP:0004020	polyhydramnios	CCO:MP0004020
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	involves: 129S4/SvJae * C57BL/6	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97603	Pkd1	Pkd1<tm1Bdgz>/Pkd1<tm1Bdgz>	involves: 129S1/Sv * 129X1/SvJ	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Ggt1-cre)1Egn/0"	involves: 129P2/OlaHsd * C57BL/6 * SJL	MP:0004153	increased renal tubule apoptosis	CCO:MP0004153
MGI:97603	Pkd1	"Nek8<jck>/Nek8<+>,Pkd1<tm1Bdgz>/Pkd1<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002116	abnormal craniofacial bone morphology	CCO:MP0002116
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000440	domed skull	CCO:MP0000440
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000457	maxilla hypoplasia	CCO:MP0000457
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000445	short snout	CCO:MP0000445
MGI:97603	Pkd1	"Pkd1<tm1.1Djmp>/Pkd1<tm1.2Djmp>,Tg(Cdh16-cre/ERT2)F427Djmp/0"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N	MP:0004969	pale kidney	CCO:MP0004969
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000104	abnormal sphenoid bone morphology	CCO:MP0000104
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0001566	hyperphosphatemia	CCO:MP0001566
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Ggt1-cre)1Egn/0"	involves: 129P2/OlaHsd * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:97603	Pkd1	Pkd1<tm1Bdgz>/Pkd1<+>	involves: 129S1/Sv * 129X1/SvJ	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0003420	delayed intramembranous bone ossification	CCO:MP0003420
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000103	nasal bone hypoplasia	CCO:MP0000103
MGI:97603	Pkd1	"Pkd1<tm1.1Djmp>/Pkd1<tm1.2Djmp>,Tg(Cdh16-cre/ERT2)F427Djmp/0"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N	MP:0003327	liver cysts	CCO:MP0003327
MGI:97603	Pkd1	"Pkd1<tm1.1Djmp>/Pkd1<tm1.2Djmp>,Tg(Cdh16-cre/ERT2)F427Djmp/0"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:97603	Pkd1	"Pkd1<tm1.1Djmp>/Pkd1<tm1.2Djmp>,Tg(Cdh16-cre/ERT2)F427Djmp/0"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:97603	Pkd1	Pkd1<tm1Bdgz>/Pkd1<+>	involves: 129S1/Sv * 129X1/SvJ	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:97603	Pkd1	Pkd1<tm1.2Djmp>/Pkd1<+>	involves: 129P2/OlaHsd * FVB/N	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:97603	Pkd1	Pkd1<tm1.2Djmp>/Pkd1<tm1.2Djmp>	involves: 129P2/OlaHsd * FVB/N	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97603	Pkd1	Pkd1<tm3.1Jzh>/Pkd1<tm3.1Jzh>	involves: 129P2/OlaHsd * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:97603	Pkd1	Pkd1<tm1Bdgz>/Pkd1<+>	involves: 129S1/Sv * 129X1/SvJ	MP:0003327	liver cysts	CCO:MP0003327
MGI:97603	Pkd1	"Pkd1<tm1.1Djmp>/Pkd1<tm1.2Djmp>,Tg(Cdh16-cre/ERT2)F427Djmp/0"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Bdgz>/Pkd1<+>	involves: 129S1/Sv * 129X1/SvJ	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Bdgz>/Pkd1<tm1Bdgz>	involves: 129S1/Sv * 129X1/SvJ	MP:0001786	skin edema	CCO:MP0001786
MGI:97603	Pkd1	Pkd1<tm1Bdgz>/Pkd1<tm1Bdgz>	involves: 129S1/Sv * 129X1/SvJ	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	"Pkd1<tm1.1Djmp>/Pkd1<tm1.1Djmp>,Tg(Cdh16-cre/ERT2)F427Djmp/0"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	"Pkd1<tm1.1Djmp>/Pkd1<tm1.2Djmp>,Tg(Cdh16-cre/ERT2)F427Djmp/0"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97603	Pkd1	"Pkd1<tm1.1Djmp>/Pkd1<tm1.2Djmp>,Tg(Cdh16-cre/ERT2)F427Djmp/0"	involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N	MP:0003917	increased kidney weight	CCO:MP0003917
MGI:97603	Pkd1	Pkd1<tm3.1Jzh>/Pkd1<tm3.1Jzh>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97603	Pkd1	Pkd1<tm3.1Jzh>/Pkd1<tm3.1Jzh>	involves: 129P2/OlaHsd * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:97603	Pkd1	Pkd1<tm1Bdgz>/Pkd1<tm1Bdgz>	involves: 129S1/Sv * 129X1/SvJ	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0003917	increased kidney weight	CCO:MP0003917
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<tm1Som>	involves: 129/Sv * C57BL/6 * SJL	MP:0001914	hemorrhage	CCO:MP0001914
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<tm1Som>	involves: 129/Sv * C57BL/6 * SJL	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<tm1Som>	involves: 129/Sv * C57BL/6 * SJL	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<tm1Som>	involves: 129/Sv * C57BL/6 * SJL	MP:0001785	edema	CCO:MP0001785
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0005178	increased circulating cholesterol level	CCO:MP0005178
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/?"	involves: 129P2/OlaHsd * CD-1	MP:0003420	delayed intramembranous bone ossification	CCO:MP0003420
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0003606	kidney failure	CCO:MP0003606
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<tm1Som>	involves: 129/Sv * C57BL/6 * SJL	MP:0003717	pallor	CCO:MP0003717
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000120	malocclusion	CCO:MP0000120
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Pkhd1-cre)1Igr/0"	involves: C57BL/6 * SJL	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004053	abnormal synchondrosis	CCO:MP0004053
MGI:97603	Pkd1	Pkd1<tm1Shh>/Pkd1<tm1Shh>	involves: 129P2/OlaHsd	MP:0001786	skin edema	CCO:MP0001786
MGI:97603	Pkd1	Pkd1<tm1Shh>/Pkd1<tm1Shh>	involves: 129P2/OlaHsd	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:97603	Pkd1	Pkd1<tm1Shh>/Pkd1<tm1Shh>	involves: 129P2/OlaHsd	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Shh>/Pkd1<tm1Shh>	involves: 129P2/OlaHsd	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0003917	increased kidney weight	CCO:MP0003917
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0003606	kidney failure	CCO:MP0003606
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<tm1Som>	involves: 129/Sv * C57BL/6 * SJL	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0001566	hyperphosphatemia	CCO:MP0001566
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<tm1Som>	involves: 129/Sv * C57BL/6 * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:97603	Pkd1	Pkd1<tm2.1Som>/Pkd1<tm2.1Som>	involves: C57BL/6 * FVB/N * SJL	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<+>	involves: 129/Sv * C57BL/6 * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	"Pkd1<tm1Som>/Pkd1<+>,Pkd2<tm1Som>/Pkd2<+>"	involves: 129/Sv * C57BL/6 * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	"Pkd1<tm1Som>/Pkd1<+>,Pkd2<tm1Som>/Pkd2<+>"	involves: 129/Sv * C57BL/6 * SJL	MP:0003327	liver cysts	CCO:MP0003327
MGI:97603	Pkd1	Pkd1<tm1Som>/Pkd1<tm1Som>	involves: 129/Sv * C57BL/6 * SJL	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Pkhd1-cre)1Igr/0"	involves: C57BL/6 * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2.1Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0005178	increased circulating cholesterol level	CCO:MP0005178
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0000440	domed skull	CCO:MP0000440
MGI:97603	Pkd1	"Pkd1<tm2Som>/Pkd1<tm2Som>,Tg(Cdh16-cre)91Igr/0"	involves: C57BL/6 * ICR * SJL	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0005273	abnormal cranial base morphology	CCO:MP0005273
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0000104	abnormal sphenoid bone morphology	CCO:MP0000104
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0006322	abnormal perichondrium morphology	CCO:MP0006322
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0004053	abnormal synchondrosis	CCO:MP0004053
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0004451	short presphenoid bone	CCO:MP0004451
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0008489	postnatal slow weight gain	CCO:MP0008489
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Tg(Wnt1-cre)11Rth/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004451	short presphenoid bone	CCO:MP0004451
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97603	Pkd1	"Pkd1<tm3Jzh>/Pkd1<tm3Jzh>,Twist2<tm1(cre)Dor>/Twist2<+>"	involves: 129P2/OlaHsd * 129X1/SvJ	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:97603	Pkd1	Pkd1<tm1.1Bol>/Pkd1<tm1.1Bol>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97603	Pkd1	Pkd1<tm1.2Bol>/Pkd1<tm1.2Bol>	Not Specified	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0001914	hemorrhage	CCO:MP0001914
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0000552	abnormal radius morphology	CCO:MP0000552
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0004686	decreased length of long bones	CCO:MP0004686
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0004174	abnormal spine curvature	CCO:MP0004174
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0005587	abnormal Meckel's cartilage morphology	CCO:MP0005587
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0005244	hemopericardium	CCO:MP0005244
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0005108	abnormal ulna morphology	CCO:MP0005108
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0000299	failure of endocardial cushion closure	CCO:MP0000299
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0002189	abnormal myocardial trabeculae morphology	CCO:MP0002189
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<+>	involves: 129S/SvEv	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0001785	edema	CCO:MP0001785
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:97603	Pkd1	Pkd1<m1Bei>/Pkd1<m1Bei>	involves: A/J * FVB/N	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<m1Bei>/Pkd1<m1Bei>	involves: A/J * FVB/N	MP:0001785	edema	CCO:MP0001785
MGI:97603	Pkd1	Pkd1<m1Bei>/Pkd1<m1Bei>	involves: A/J * FVB/N	MP:0003068	enlarged kidney	CCO:MP0003068
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:97603	Pkd1	Pkd1<m1Bei>/Pkd1<m1Bei>	involves: A/J * FVB/N	MP:0003450	enlarged pancreas	CCO:MP0003450
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0000164	abnormal cartilage development	CCO:MP0000164
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0002116	abnormal craniofacial bone morphology	CCO:MP0002116
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<+>	involves: 129S/SvEv	MP:0003327	liver cysts	CCO:MP0003327
MGI:97603	Pkd1	Pkd1<tm1Rsa>/Pkd1<tm1Rsa>	involves: 129S/SvEv	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0001270	distended abdomen	CCO:MP0001270
MGI:97603	Pkd1	Pkd1<tm1.1Djmp>/Pkd1<tm1.1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0006278	aortic aneurysm	CCO:MP0006278
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0003266	biliary cyst	CCO:MP0003266
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0003253	dilated bile duct	CCO:MP0003253
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0003215	renal interstitial fibrosis	CCO:MP0003215
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003215	renal interstitial fibrosis	CCO:MP0003215
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0001270	distended abdomen	CCO:MP0001270
MGI:97603	Pkd1	Pkd1<tm1Djmp>/Pkd1<tm1Djmp>	involves: 129P2/OlaHsd * C57BL/6	MP:0001859	kidney inflammation	CCO:MP0001859
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0001786	skin edema	CCO:MP0001786
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003327	liver cysts	CCO:MP0003327
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002427	disproportionate dwarf	CCO:MP0002427
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003641	small lung	CCO:MP0003641
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0001265	decreased body size	CCO:MP0001265
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002136	abnormal kidney physiology	CCO:MP0002136
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0001178	pulmonary hypoplasia	CCO:MP0001178
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0004020	polyhydramnios	CCO:MP0004020
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003068	enlarged kidney	CCO:MP0003068
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003014	abnormal kidney medulla morphology	CCO:MP0003014
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0005297	spina bifida occulta	CCO:MP0005297
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002657	chondrodystrophy	CCO:MP0002657
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0000522	kidney cortex cysts	CCO:MP0000522
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0001954	respiratory distress	CCO:MP0001954
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm1Ggg>	Not Specified	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0005328	abnormal circulating creatinine level	CCO:MP0005328
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0009145	abnormal pancreatic acinus morphology	CCO:MP0009145
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0009144	dilated pancreatic duct	CCO:MP0009144
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003338	pancreas lipomatosis	CCO:MP0003338
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003334	pancreas fibrosis	CCO:MP0003334
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003325	decreased liver function	CCO:MP0003325
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0003254	bile duct inflammation	CCO:MP0003254
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0001270	distended abdomen	CCO:MP0001270
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002928	abnormal bile duct morphology	CCO:MP0002928
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0009168	decreased pancreatic islet number	CCO:MP0009168
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0005220	abnormal exocrine pancreas morphology	CCO:MP0005220
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0001859	kidney inflammation	CCO:MP0001859
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0000608	dissociated hepatocytes	CCO:MP0000608
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0009168	decreased pancreatic islet number	CCO:MP0009168
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0009144	dilated pancreatic duct	CCO:MP0009144
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0009050	dilated proximal convoluted tubules	CCO:MP0009050
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0004967	abnormal kidney epithelium morphology	CCO:MP0004967
MGI:97603	Pkd1	Pkd1<tm1Jzh>/Pkd1<tm1Jzh>	either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c)	MP:0002260	abnormal thyroid cartilage morphology	CCO:MP0002260
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm1Ggg>	either: (involves: 129/Sv) or (involves: 129/Sv * Black Swiss)	MP:0004020	polyhydramnios	CCO:MP0004020
MGI:97603	Pkd1	Pkd1<tm2.1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0005297	spina bifida occulta	CCO:MP0005297
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0002657	chondrodystrophy	CCO:MP0002657
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm1Ggg>	involves: 129/Sv * Black Swiss	MP:0004020	polyhydramnios	CCO:MP0004020
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0001786	skin edema	CCO:MP0001786
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0000065	abnormal bone marrow cavity morphology	CCO:MP0000065
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0002113	abnormal skeleton development	CCO:MP0002113
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0002427	disproportionate dwarf	CCO:MP0002427
MGI:97603	Pkd1	Pkd1<tm2.1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0002083	premature death	CCO:MP0002083
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0002260	abnormal thyroid cartilage morphology	CCO:MP0002260
MGI:97603	Pkd1	Pkd1<tm2.1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0004020	polyhydramnios	CCO:MP0004020
MGI:97603	Pkd1	"Pkd1<tm2Ggg>/Pkd1<tm2Ggg>,Tg(MMTV-cre)4Mam/0"	involves: 129S4/SvJae * FVB	MP:0003327	liver cysts	CCO:MP0003327
MGI:97603	Pkd1	"Pkd1<tm2Ggg>/Pkd1<tm2Ggg>,Tg(MMTV-cre)4Mam/0"	involves: 129S4/SvJae * FVB	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm1Ggg>	involves: 129/Sv * Black Swiss	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm1Ggg>	involves: 129/Sv * Black Swiss	MP:0001785	edema	CCO:MP0001785
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm1Ggg>	involves: 129/Sv * Black Swiss	MP:0001914	hemorrhage	CCO:MP0001914
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm1Ggg>	Not Specified	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0003327	liver cysts	CCO:MP0003327
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0002896	abnormal bone mineralization	CCO:MP0002896
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0008528	polycystic kidney	CCO:MP0008528
MGI:97603	Pkd1	Pkd1<tm2.1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97603	Pkd1	Pkd1<tm2.1Ggg>/Pkd1<tm2.1Ggg>	involves: 129S4/SvJae * Black Swiss * C57BL/6	MP:0001784	abnormal fluid regulation	CCO:MP0001784
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0003215	renal interstitial fibrosis	CCO:MP0003215
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0004686	decreased length of long bones	CCO:MP0004686
MGI:97603	Pkd1	Pkd1<tm1Ggg>/Pkd1<tm1Ggg>	Not Specified	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0004020	polyhydramnios	CCO:MP0004020
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0001924	infertility	CCO:MP0001924
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<+>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0003675	kidney cysts	CCO:MP0003675
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0002113	abnormal skeleton development	CCO:MP0002113
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0003420	delayed intramembranous bone ossification	CCO:MP0003420
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0003419	delayed endochondral bone ossification	CCO:MP0003419
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0003409	decreased width of hypertrophic chondrocyte zone	CCO:MP0003409
MGI:97603	Pkd1	Pkd1<tm2Jzh>/Pkd1<tm2Jzh>	either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6)	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:97603	Pkd1	Pkd1<tm1Hung>/Pkd1<tm1Hung>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB)	MP:0003068	enlarged kidney	CCO:MP0003068
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0003253	dilated bile duct	CCO:MP0003253
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0003327	liver cysts	CCO:MP0003327
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<+>	involves: 129/Sv * C57BL/6 * SJL	MP:0003327	liver cysts	CCO:MP0003327
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	"Pkd1<tm1Som>/Pkd1<+>,Pkd2<tm1Som>/Pkd2<+>"	involves: 129/Sv * C57BL/6 * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0003881	abnormal nephron morphology	CCO:MP0003881
MGI:1099818	Pkd2	"Pkd1<tm1Som>/Pkd1<+>,Pkd2<tm1Som>/Pkd2<+>"	involves: 129/Sv * C57BL/6 * SJL	MP:0003327	liver cysts	CCO:MP0003327
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0009050	dilated proximal convoluted tubules	CCO:MP0009050
MGI:1099818	Pkd2	Pkd2<lrm4>/Pkd2<lrm4>	involves: BALB/cAnN * C3H/HeH	MP:0002766	situs inversus	CCO:MP0002766
MGI:1099818	Pkd2	Pkd2<lrm4>/Pkd2<lrm4>	involves: BALB/cAnN * C3H/HeH	MP:0003178	left pulmonary isomerism	CCO:MP0003178
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0009144	dilated pancreatic duct	CCO:MP0009144
MGI:1099818	Pkd2	Pkd2<lrm4>/Pkd2<lrm4>	involves: BALB/cAnN * C3H/HeH	MP:0003283	abnormal digestive organ placement	CCO:MP0003283
MGI:1099818	Pkd2	Pkd2<lrm4>/Pkd2<lrm4>	involves: BALB/cAnN * C3H/HeH	MP:0001785	edema	CCO:MP0001785
MGI:1099818	Pkd2	"Pkd2<tm1Som>/Pkd2<+>,Pkhd1<tm1Gwu>/Pkhd1<tm1Gwu>"	involves: 129/Sv * C57BL/6J * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	Pkd2<lrm4>/Pkd2<lrm4>	involves: BALB/cAnN * C3H/HeH	MP:0000650	mesocardia	CCO:MP0000650
MGI:1099818	Pkd2	"Pkd2<tm1Som>/Pkd2<+>,Pkhd1<tm1Gwu>/Pkhd1<tm1Gwu>"	involves: 129/Sv * C57BL/6J * SJL	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:1099818	Pkd2	Pkd2<lrm4>/Pkd2<lrm4>	involves: BALB/cAnN * C3H/HeH	MP:0000644	dextrocardia	CCO:MP0000644
MGI:1099818	Pkd2	Pkd2<tm1Gwu>/Pkd2<tm1Gwu>	involves: C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:1099818	Pkd2	Pkd2<lrm4>/Pkd2<lrm4>	involves: BALB/cAnN * C3H/HeH	MP:0000531	right pulmonary isomerism	CCO:MP0000531
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002766	situs inversus	CCO:MP0002766
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm1Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0004020	polyhydramnios	CCO:MP0004020
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm1Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0001785	edema	CCO:MP0001785
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002767	situs ambiguus	CCO:MP0002767
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0006113	abnormal heart septum morphology	CCO:MP0006113
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0005312	pericardial effusion	CCO:MP0005312
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0006107	abnormal atrioventricular canal morphology	CCO:MP0006107
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000269	abnormal looping morphogenesis	CCO:MP0000269
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000690	absent spleen	CCO:MP0000690
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001944	abnormal pancreas morphology	CCO:MP0001944
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000522	kidney cortex cysts	CCO:MP0000522
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0004190	abnormal direction of embryo turning	CCO:MP0004190
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001706	abnormal left-right axis patterning	CCO:MP0001706
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0000596	abnormal liver development	CCO:MP0000596
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0004066	abnormal primitive node morphology	CCO:MP0004066
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm1Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm1Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003327	liver cysts	CCO:MP0003327
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm1Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0000522	kidney cortex cysts	CCO:MP0000522
MGI:1099818	Pkd2	Pkd2<tm1Dwo>/Pkd2<tm1Dwo>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0001176	abnormal lung development	CCO:MP0001176
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0003327	liver cysts	CCO:MP0003327
MGI:1099818	Pkd2	Pkd2<tm2Som>/Pkd2<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003327	liver cysts	CCO:MP0003327
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003675	kidney cysts	CCO:MP0003675
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003255	bile duct proliferation	CCO:MP0003255
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003606	kidney failure	CCO:MP0003606
MGI:1099818	Pkd2	Pkd2<tm1Som>/Pkd2<tm2Som>	involves: 129/Sv * C57BL/6J * SJL	MP:0003336	pancreas cysts	CCO:MP0003336
MGI:104747	Pkia	Pkia<tm1Idz>/Pkia<tm1Idz>	involves: 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:104747	Pkia	"Pkia<tm1Idz>/Pkia<tm1Idz>,Pkib<tm1Idz>/Pkib<tm1Idz>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0004024	aneuploidy	CCO:MP0004024
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<Gt(RRR358)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<Gt(RRR358)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<Gt(RRR358)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:97621	Plk1	Plk1<Gt(RRR358)Byg>/Plk1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0008714	lung carcinoma	CCO:MP0008714
MGI:1099790	Plk2	Plk2<tm1Elan>/Plk2<tm1Elan>	involves: C57BL/6NTac	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1099790	Plk2	Plk2<tm1Rle>/Plk2<tm1Rle>	either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1099790	Plk2	Plk2<tm1Rle>/Plk2<tm1Rle>	either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1)	MP:0001712	abnormal placenta development	CCO:MP0001712
MGI:1099790	Plk2	Plk2<tm1Rle>/Plk2<tm1Rle>	either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1)	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:1099790	Plk2	Plk2<tm1Rle>/Plk2<tm1Rle>	either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1)	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:1099790	Plk2	Plk2<tm1Rle>/Plk2<tm1Rle>	either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1)	MP:0001265	decreased body size	CCO:MP0001265
MGI:1099790	Plk2	Plk2<tm1Rle>/Plk2<tm1Rle>	either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1)	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:109604	Plk3	Plk3<tm1Dai>/Plk3<tm1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0002035	leiomyosarcoma	CCO:MP0002035
MGI:109604	Plk3	Plk3<tm1Dai>/Plk3<tm1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:109604	Plk3	Plk3<tm1Dai>/Plk3<tm1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0003721	increased tumor growth/size	CCO:MP0003721
MGI:109604	Plk3	Plk3<tm1Dai>/Plk3<tm1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0008014	lung tumor	CCO:MP0008014
MGI:109604	Plk3	Plk3<tm1Dai>/Plk3<tm1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0008019	liver tumor	CCO:MP0008019
MGI:109604	Plk3	Plk3<tm1Dai>/Plk3<tm1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0008714	lung carcinoma	CCO:MP0008714
MGI:109604	Plk3	Plk3<tm1Dai>/Plk3<tm1Dai>	involves: 129S4/SvJae * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0001601	abnormal myelopoiesis	CCO:MP0001601
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0000716	abnormal immune system cell morphology	CCO:MP0000716
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0000334	decreased granulocyte number	CCO:MP0000334
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0002022	lymphoma	CCO:MP0002022
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:104662	Pml	Pml<tm1Ppp>/Pml<tm1Ppp>	involves: 129S7/SvEvBrd	MP:0002412	increased susceptibility to bacterial infection	CCO:MP0002412
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0008569	lethality at weaning	CCO:MP0008569
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0003871	abnormal myelin sheath morphology	CCO:MP0003871
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0001922	reduced male fertility	CCO:MP0001922
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0002882	abnormal neuron morphology	CCO:MP0002882
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0002566	abnormal sexual interaction	CCO:MP0002566
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0001513	limb grasping	CCO:MP0001513
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0000755	hindlimb paralysis	CCO:MP0000755
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0000747	muscle weakness	CCO:MP0000747
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0000947	convulsive seizures	CCO:MP0000947
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<+>	Not Specified	MP:0002066	abnormal motor capabilities/coordination/movement	CCO:MP0002066
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0000756	forelimb paralysis	CCO:MP0000756
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0000755	hindlimb paralysis	CCO:MP0000755
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0000921	demyelination	CCO:MP0000921
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0000921	demyelination	CCO:MP0000921
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<tm1Lnot>	Not Specified	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<tm1Lnot>/Pmp22<+>	Not Specified	MP:0003871	abnormal myelin sheath morphology	CCO:MP0003871
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<+>	Not Specified	MP:0001265	decreased body size	CCO:MP0001265
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv * C57BL/6	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	B6.Cg-Pmp22<Tr-J> Krt25<Re>/+ +/J	MP:0008260	abnormal autophagy	CCO:MP0008260
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<+>	involves: 129S/SvEv	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<+>	involves: 129S/SvEv	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv	MP:0008814	reduced nerve conduction velocity	CCO:MP0008814
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv	MP:0003871	abnormal myelin sheath morphology	CCO:MP0003871
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv	MP:0005402	abnormal action potential	CCO:MP0005402
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv	MP:0000755	hindlimb paralysis	CCO:MP0000755
MGI:97631	Pmp22	Pmp22<Tr-Ncnp>/Pmp22<+>	GAD/Ncnp-Pmp22<Tr-Ncnp>	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv	MP:0000947	convulsive seizures	CCO:MP0000947
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv * C57BL/6	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0005405	axon degeneration	CCO:MP0005405
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001515	abnormal grip strength	CCO:MP0001515
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001402	hypoactivity	CCO:MP0001402
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001523	impaired righting response	CCO:MP0001523
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0005405	axon degeneration	CCO:MP0005405
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<tm1Ueli>	involves: 129S/SvEv	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0005405	axon degeneration	CCO:MP0005405
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<+>	involves: 129S/SvEv	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0000921	demyelination	CCO:MP0000921
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001515	abnormal grip strength	CCO:MP0001515
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0001523	impaired righting response	CCO:MP0001523
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<tm1Ueli>/Pmp22<+>	involves: 129S/SvEv	MP:0003871	abnormal myelin sheath morphology	CCO:MP0003871
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0001402	hypoactivity	CCO:MP0001402
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001402	hypoactivity	CCO:MP0001402
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0001515	abnormal grip strength	CCO:MP0001515
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001523	impaired righting response	CCO:MP0001523
MGI:97631	Pmp22	Pmp22<Tr>/?	involves: CBA	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0000921	demyelination	CCO:MP0000921
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0000921	demyelination	CCO:MP0000921
MGI:97631	Pmp22	Pmp22<Tr-3H>/Pmp22<+>	involves: BALB/cCruk * C3H/HeH	MP:0001405	impaired coordination	CCO:MP0001405
MGI:97631	Pmp22	Pmp22<Tr>/?	Not Specified	MP:0002064	seizures	CCO:MP0002064
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<Tr>	Not Specified	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<Tr-J>	involves: C57BL/6	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<Tr-J>	involves: C57BL/6	MP:0001516	abnormal motor coordination/ balance	CCO:MP0001516
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<Tr-J>	involves: C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97631	Pmp22	Pmp22<Tr-Ncnp>/Pmp22<+>	GAD/Ncnp-Pmp22<Tr-Ncnp>	MP:0000921	demyelination	CCO:MP0000921
MGI:97631	Pmp22	Pmp22<Tr>/?	Not Specified	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<Tr>	Not Specified	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<Tr>/?	Not Specified	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<Tr>/?	Not Specified	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-J>/?	involves: C57BL/6	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-J>/?	involves: C57BL/6	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:97631	Pmp22	Pmp22<Tr-J>/?	involves: C57BL/6	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<Tr-J>/?	involves: C57BL/6	MP:0000745	tremors	CCO:MP0000745
MGI:97631	Pmp22	Pmp22<Tr-Ncnp>/Pmp22<Tr-Ncnp>	GAD/Ncnp-Pmp22<Tr-Ncnp>	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<Tr-Ncnp>/Pmp22<Tr-Ncnp>	GAD/Ncnp-Pmp22<Tr-Ncnp>	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:97631	Pmp22	Pmp22<Tr-Ncnp>/Pmp22<Tr-Ncnp>	GAD/Ncnp-Pmp22<Tr-Ncnp>	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H/HeN	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	B6.Cg-Pmp22<Tr-J> Krt25<Re>/+ +/J	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:97631	Pmp22	Pmp22<Tr>/?	Not Specified	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<Tr>	Not Specified	MP:0000921	demyelination	CCO:MP0000921
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	B6.Cg-Pmp22<Tr-J> Krt25<Re>/+ +/J	MP:0005402	abnormal action potential	CCO:MP0005402
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	involves: C57BL/6	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	involves: C57BL/6	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	involves: C57BL/6	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	involves: C57BL/6	MP:0000920	abnormal myelination	CCO:MP0000920
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	involves: C57BL/6	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	involves: C57BL/6	MP:0001405	impaired coordination	CCO:MP0001405
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	involves: C57BL/6	MP:0000749	muscle degeneration	CCO:MP0000749
MGI:97631	Pmp22	Pmp22<Tr>/Pmp22<Tr>	Not Specified	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:97631	Pmp22	Pmp22<Tr-J>/Pmp22<+>	B6.Cg-Pmp22<Tr-J> Krt25<Re>/+ +/J	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:97631	Pmp22	Pmp22<Tr-1H>/Pmp22<+>	involves: BALB/c * C3H	MP:0000921	demyelination	CCO:MP0000921
MGI:97631	Pmp22	Pmp22<Tr-2H>/Pmp22<+>	involves: BALB/c * C3H	MP:0000921	demyelination	CCO:MP0000921
MGI:104288	Pms2	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:104288	Pms2	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:104288	Pms2	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:104288	Pms2	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:104288	Pms2	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	MP:0002686	globozoospermia	CCO:MP0002686
MGI:104288	Pms2	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	MP:0008892	abnormal sperm flagellum morphology	CCO:MP0008892
MGI:104288	Pms2	Pms2<tm1Lisk>/Pms2<tm1Lisk>	involves: 129S2/SvPas * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:1858214	Ppm1d	"Mapk14<tm1Dvb>/Mapk14<+>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1858214	Ppm1d	"Ppm1d<tm1Lad>/Ppm1d<+>,Tg(IghMyc)22Bri/0"	involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1858214	Ppm1d	"Ppm1d<tm1Lad>/Ppm1d<+>,Tg(IghMyc)22Bri/0"	involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1858214	Ppm1d	"Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1858214	Ppm1d	"Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1858214	Ppm1d	"Mapk14<tm1Dvb>/Mapk14<+>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129S7/SvEvBrd * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1858214	Ppm1d	"Cdkn2a<tm1Cjs>/Cdkn2a<+>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129 * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1858214	Ppm1d	"Cdkn2a<tm1Cjs>/Cdkn2a<+>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129 * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1858214	Ppm1d	"Atm<tm1Awb>/Atm<tm1Awb>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129 * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1858214	Ppm1d	"Atm<tm1Awb>/Atm<tm1Awb>,Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0"	involves: 129 * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1858214	Ppm1d	"Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129 * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1858214	Ppm1d	"Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129 * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008074	increased CD4-positive T cell number	CCO:MP0008074
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002631	abnormal epididymis morphology	CCO:MP0002631
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000706	small thymus	CCO:MP0000706
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005093	decreased B cell proliferation	CCO:MP0005093
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002418	increased susceptibility to viral infection	CCO:MP0002418
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000688	lymphoid hyperplasia	CCO:MP0000688
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002499	chronic inflammation	CCO:MP0002499
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001154	seminiferous tubule degeneration	CCO:MP0001154
MGI:1858214	Ppm1d	Ppm1d<tm1Lad>/Ppm1d<tm1Lad>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001212	skin lesions	CCO:MP0001212
MGI:106065	Ppm1g	Ppm1g<tm1Dgen>/Ppm1g<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:106065	Ppm1g	Ppm1g<tm1Dgen>/Ppm1g<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0009142	decreased prepulse inhibition	CCO:MP0009142
MGI:104871	Ppp1cb	Ppp1cb<Gt(OST319712)Lex>/Ppp1cb<Gt(OST319712)Lex>	involves: 129S5/SvEvBrd * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:104872	Ppp1cc	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001147	small testis	CCO:MP0001147
MGI:104872	Ppp1cc	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001932	abnormal spermiogenesis	CCO:MP0001932
MGI:104872	Ppp1cc	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001925	male infertility	CCO:MP0001925
MGI:104872	Ppp1cc	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:104872	Ppp1cc	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:104872	Ppp1cc	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:104872	Ppp1cc	Ppp1cc<tm1Var>/Ppp1cc<tm1Var>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:1321159	Ppp2ca	Ppp2ca<tm1Gotz>/Ppp2ca<tm1Gotz>	involves: 129/Sv * C57BL/6	MP:0001683	absent mesoderm	CCO:MP0001683
MGI:1321159	Ppp2ca	Ppp2ca<tm1Gotz>/Ppp2ca<tm1Gotz>	involves: 129/Sv * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1321159	Ppp2ca	Ppp2ca<tm1Gotz>/Ppp2ca<tm1Gotz>	involves: 129/Sv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1321159	Ppp2ca	Ppp2ca<tm1Gotz>/Ppp2ca<tm1Gotz>	involves: 129/Sv * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0005558	decreased creatinine clearance	CCO:MP0005558
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0009406	decreased skeletal muscle fiber number	CCO:MP0009406
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0002083	premature death	CCO:MP0002083
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae * Black Swiss	MP:0002761	abnormal hippocampal mossy fiber morphology	CCO:MP0002761
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0001262	decreased body weight	CCO:MP0001262
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<+>	involves: 129S4/SvJae	MP:0002987	abnormal urine osmolality	CCO:MP0002987
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0009409	abnormal skeletal muscle fiber type ratio	CCO:MP0009409
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0009401	increased skeletal muscle fiber diameter	CCO:MP0009401
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0002988	decreased urine osmolality	CCO:MP0002988
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0000195	hypocalcemia	CCO:MP0000195
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	involves: 129S4/SvJae	MP:0005553	increased circulating creatinine level	CCO:MP0005553
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	either: (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6)	MP:0008567	decreased interferon-gamma secretion	CCO:MP0008567
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	either: (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6)	MP:0008700	decreased interleukin-4 secretion	CCO:MP0008700
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	either: (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6)	MP:0008688	decreased interleukin-2 secretion	CCO:MP0008688
MGI:107164	Ppp3ca	Ppp3ca<tm1Jse>/Ppp3ca<tm1Jse>	either: (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6)	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0005159	azoospermia	CCO:MP0005159
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0001130	abnormal ovarian folliculogenesis	CCO:MP0001130
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0001926	female infertility	CCO:MP0001926
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0001925	male infertility	CCO:MP0001925
MGI:2384854	Prdm9	Prdm9<tm1Ymat>/Prdm9<tm1Ymat>	Not Specified	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:97772	Prox1	Prox1<tm3(cre/ESR1)Gco>/Prox1<tm3(cre/ESR1)Gco>	involves: 129S1/Sv	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97772	Prox1	"Prox1<tm1Gco>/Prox1<tm2Gco>,Tg(Tek-cre)1Ywa/?"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0001879	abnormal lymphatic vessel morphology	CCO:MP0001879
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0003212	increased susceptibility to age related obesity	CCO:MP0003212
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0005317	increased triglyceride level	CCO:MP0005317
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0005425	increased macrophage cell number	CCO:MP0005425
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0005669	increased circulating leptin level	CCO:MP0005669
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0006094	increased fat cell size	CCO:MP0006094
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0003659	abnormal lymph circulation	CCO:MP0003659
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0003660	chylothorax	CCO:MP0003660
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0008908	increased total fat pad weight	CCO:MP0008908
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ	MP:0003659	abnormal lymph circulation	CCO:MP0003659
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0005453	increased adipose tissue amount	CCO:MP0005453
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001879	abnormal lymphatic vessel morphology	CCO:MP0001879
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0002450	abnormal lymph organ development	CCO:MP0002450
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0000596	abnormal liver development	CCO:MP0000596
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0000601	small liver	CCO:MP0000601
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001785	edema	CCO:MP0001785
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0004001	decreased hepatocyte proliferation	CCO:MP0004001
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0004247	small pancreas	CCO:MP0004247
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0008107	absent horizontal cells	CCO:MP0008107
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0009159	increased pancreatic acinar cell number	CCO:MP0009159
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0002712	increased circulating glucagon level	CCO:MP0002712
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<tm1Gco>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0009165	abnormal endocrine pancreas morphology	CCO:MP0009165
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001436	abnormal suckling behavior	CCO:MP0001436
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001785	edema	CCO:MP0001785
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001846	increased inflammatory response	CCO:MP0001846
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001402	hypoactivity	CCO:MP0001402
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001570	abnormal circulating enzyme level	CCO:MP0001570
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001575	cyanosis	CCO:MP0001575
MGI:97772	Prox1	Prox1<tm1Gco>/Prox1<+>	involves: 129S1/Sv * 129X1/SvJ * NMRI	MP:0001954	respiratory distress	CCO:MP0001954
MGI:97772	Prox1	"Prox1<tm2Gco>/Prox1<+>,Tg(Tek-cre)1Ywa/0"	involves: 129S1/Sv * C57BL/6 * NMRI * SJL	MP:0003660	chylothorax	CCO:MP0003660
MGI:97772	Prox1	"Prox1<tm2Gco>/Prox1<+>,Tg(Tek-cre)1Ywa/0"	involves: 129S1/Sv * C57BL/6 * NMRI * SJL	MP:0003659	abnormal lymph circulation	CCO:MP0003659
MGI:97772	Prox1	"Prox1<tm2Gco>/Prox1<+>,Tg(Tek-cre)1Ywa/0"	involves: 129S1/Sv * C57BL/6 * NMRI * SJL	MP:0003212	increased susceptibility to age related obesity	CCO:MP0003212
MGI:97772	Prox1	"Prox1<tm2Gco>/Prox1<+>,Tg(Tek-cre)1Ywa/0"	involves: 129S1/Sv * C57BL/6 * NMRI * SJL	MP:0001785	edema	CCO:MP0001785
MGI:97772	Prox1	"Prox1<tm2Gco>/Prox1<+>,Tg(Tek-cre)1Ywa/0"	involves: 129S1/Sv * C57BL/6 * NMRI * SJL	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:97772	Prox1	"Prox1<tm2Gco>/Prox1<+>,Tg(Tek-cre)1Ywa/0"	involves: 129S1/Sv * C57BL/6 * NMRI * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97772	Prox1	"Prox1<tm2Gco>/Prox1<+>,Tg(Tek-cre)1Ywa/0"	involves: 129S1/Sv * C57BL/6 * NMRI * SJL	MP:0001879	abnormal lymphatic vessel morphology	CCO:MP0001879
MGI:1098610	Psmc3ip	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1098610	Psmc3ip	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	MP:0003582	abnormal ovary development	CCO:MP0003582
MGI:1098610	Psmc3ip	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	MP:0005159	azoospermia	CCO:MP0005159
MGI:1098610	Psmc3ip	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1098610	Psmc3ip	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001940	testicular hypoplasia	CCO:MP0001940
MGI:1098610	Psmc3ip	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001117	absent gametes	CCO:MP0001117
MGI:1098610	Psmc3ip	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001930	abnormal meiosis	CCO:MP0001930
MGI:1098610	Psmc3ip	Psmc3ip<tm1Rdco>/Psmc3ip<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001924	infertility	CCO:MP0001924
MGI:1096366	Psme3	Psme3<tm1Jjm>/Psme3<tm1Jjm>	B6.129X1-Psme3<tm1Jjm>	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096366	Psme3	Psme3<tm1Tchi>/Psme3<tm1Tchi>	involves: C57BL/6J * CBA	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1096366	Psme3	Psme3<tm1Jjm>/Psme3<tm1Jjm>	B6.129X1-Psme3<tm1Jjm>	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:1096366	Psme3	Psme3<tm1Jjm>/Psme3<tm1Jjm>	B6.129X1-Psme3<tm1Jjm>	MP:0005399	increased susceptibility to fungal infection	CCO:MP0005399
MGI:1096366	Psme3	Psme3<tm1Tchi>/Psme3<tm1Tchi>	involves: C57BL/6J * CBA	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1096366	Psme3	Psme3<tm1Jjm>/Psme3<tm1Jjm>	B6.129X1-Psme3<tm1Jjm>	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:99511	Ptpn11	"Ptpn11<tm1Ambt>/Ptpn11<tm1Ambt>,Tg(Ckmm-cre)5Khn/0"	involves: 129/Sv * C57BL/6 * FVB	MP:0009400	decreased skeletal muscle fiber size	CCO:MP0009400
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ	MP:0004025	polyploidy	CCO:MP0004025
MGI:99511	Ptpn11	"Ptpn11<tm1Ambt>/Ptpn11<tm1Ambt>,Tg(Ckmm-cre)5Khn/0"	involves: 129/Sv * C57BL/6 * FVB	MP:0009406	decreased skeletal muscle fiber number	CCO:MP0009406
MGI:99511	Ptpn11	Ptpn11<tm2Bgn>/Ptpn11<tm2Bgn>	involves: 129S4/SvJae	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:99511	Ptpn11	Ptpn11<tm2Bgn>/Ptpn11<tm2Bgn>	involves: 129S4/SvJae	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:99511	Ptpn11	Ptpn11<tm2Bgn>/Ptpn11<tm2Bgn>	involves: 129S4/SvJae	MP:0003988	disorganized embryonic tissue	CCO:MP0003988
MGI:99511	Ptpn11	Ptpn11<tm1Yan>/Ptpn11<tm1Yan>	involves: 129S4/SvJae * C57BL/6J	MP:0008527	embryonic lethality at implantation	CCO:MP0008527
MGI:99511	Ptpn11	Ptpn11<tm1Yan>/Ptpn11<tm1Yan>	involves: 129S4/SvJae * C57BL/6J	MP:0004957	abnormal blastocyst morphology	CCO:MP0004957
MGI:99511	Ptpn11	Ptpn11<tm1Yan>/Ptpn11<tm1Yan>	involves: 129S4/SvJae * C57BL/6J	MP:0005028	abnormal trophectoderm morphology	CCO:MP0005028
MGI:99511	Ptpn11	Ptpn11<tm1Yan>/Ptpn11<tm1Yan>	involves: 129S4/SvJae * C57BL/6J	MP:0001685	abnormal endoderm development	CCO:MP0001685
MGI:99511	Ptpn11	Ptpn11<tm1Yan>/Ptpn11<tm1Yan>	involves: 129S4/SvJae * C57BL/6J	MP:0001729	impaired embryo implantation	CCO:MP0001729
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6	MP:0001300	ocular hypertelorism	CCO:MP0001300
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000220	increased monocyte cell number	CCO:MP0000220
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0001577	anemia	CCO:MP0001577
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0002429	abnormal blood cell morphology/development	CCO:MP0002429
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000322	increased granulocyte number	CCO:MP0000322
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000599	enlarged liver	CCO:MP0000599
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000172	abnormal bone marrow cell number	CCO:MP0000172
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(CAG-cre/Esr1)5Amc/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0005460	abnormal leukopoiesis	CCO:MP0005460
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6	MP:0001258	decreased body length	CCO:MP0001258
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0001300	ocular hypertelorism	CCO:MP0001300
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0003808	increased endocardial cushion size	CCO:MP0003808
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0000442	longitudinally short skull	CCO:MP0000442
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0005460	abnormal leukopoiesis	CCO:MP0005460
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6	MP:0008825	abnormal cardiac epithelial to mesenchymal transition	CCO:MP0008825
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	C.129S4-Ptpn11<tm1Bgn>	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	B6.129S4-Ptpn11<tm1Bgn>	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	B6.129S4-Ptpn11<tm1Bgn>	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<+>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0001258	decreased body length	CCO:MP0001258
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0008989	abnormal liver sinusoid morphology	CCO:MP0008989
MGI:99511	Ptpn11	"Meox2<tm1(cre)Sor>/Meox2<+>,Ptpn11<tm1Toa>/Ptpn11<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:99511	Ptpn11	"Meox2<tm1(cre)Sor>/Meox2<+>,Ptpn11<tm1Toa>/Ptpn11<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:99511	Ptpn11	"Meox2<tm1(cre)Sor>/Meox2<+>,Ptpn11<tm1Toa>/Ptpn11<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:99511	Ptpn11	"Meox2<tm1(cre)Sor>/Meox2<+>,Ptpn11<tm1Toa>/Ptpn11<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:99511	Ptpn11	"Meox2<tm1(cre)Sor>/Meox2<+>,Ptpn11<tm1Toa>/Ptpn11<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:99511	Ptpn11	"Meox2<tm1(cre)Sor>/Meox2<+>,Ptpn11<tm1Toa>/Ptpn11<+>"	involves: 129S6/SvEvTac * C57BL/6	MP:0003958	heart valve hyperplasia	CCO:MP0003958
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Tek-cre)12Flv/0"	involves: 129S6/SvEvTac * C3H * C57BL/6	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Tek-cre)12Flv/0"	involves: 129S6/SvEvTac * C3H * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Tek-cre)12Flv/0"	involves: 129S6/SvEvTac * C3H * C57BL/6	MP:0003808	increased endocardial cushion size	CCO:MP0003808
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Tek-cre)12Flv/0"	involves: 129S6/SvEvTac * C3H * C57BL/6	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0008475	intermingled spleen red and white pulp	CCO:MP0008475
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Wnt1-cre)11Rth/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA/J	MP:0000442	longitudinally short skull	CCO:MP0000442
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0008813	decreased common myeloid progenitor cell number	CCO:MP0008813
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Wnt1-cre)11Rth/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA/J	MP:0001300	ocular hypertelorism	CCO:MP0001300
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Mx1-cre)1Cgn/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA	MP:0008826	abnormal splenic cell ratio	CCO:MP0008826
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0000442	longitudinally short skull	CCO:MP0000442
MGI:99511	Ptpn11	Ptpn11<tm2.1Toa>/Ptpn11<tm2.1Toa>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6	MP:0001258	decreased body length	CCO:MP0001258
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(EIIa-cre)C5379Lmgd/0"	involves: 129S6/SvEvTac * FVB/N	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:99511	Ptpn11	"Ptpn11<tm1Toa>/Ptpn11<+>,Tg(Tek-cre)12Flv/0"	involves: 129S6/SvEvTac * C3H * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001179	thick alveolar septum	CCO:MP0001179
MGI:99511	Ptpn11	Ptpn11<tm1Rbn>/Ptpn11<tm1Rbn>	involves: 129 * Black Swiss	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001726	abnormal allantois morphology	CCO:MP0001726
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0006117	aortic valve stenosis	CCO:MP0006117
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0006138	congestive heart failure	CCO:MP0006138
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0003233	prolonged QT interval	CCO:MP0003233
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0006047	aortic valve regurgitation	CCO:MP0006047
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0003137	abnormal impulse conducting system conduction	CCO:MP0003137
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0002842	increased blood pressure	CCO:MP0002842
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0001625	cardiac hypertrophy	CCO:MP0001625
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0002748	abnormal pulmonary valve morphology	CCO:MP0002748
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0002747	abnormal aortic valve morphology	CCO:MP0002747
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0002746	abnormal semilunar valve morphology	CCO:MP0002746
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0003820	increased left ventricle systolic pressure	CCO:MP0003820
MGI:99511	Ptpn11	Ptpn11<tm1Rbn>/Ptpn11<+>	involves: 129 * Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0003898	abnormal QRS complex	CCO:MP0003898
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0004180	failure of initiation of embryo turning	CCO:MP0004180
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0004076	abnormal vitelline vascular remodeling	CCO:MP0004076
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0003400	kinked neural tube	CCO:MP0003400
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002825	abnormal notochord morphology	CCO:MP0002825
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0005221	abnormal rostral-caudal axis patterning	CCO:MP0005221
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001684	abnormal axial mesoderm	CCO:MP0001684
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001689	incomplete somite formation	CCO:MP0001689
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000929	open neural tube	CCO:MP0000929
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001177	atelectasis	CCO:MP0001177
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0000410	waved hair	CCO:MP0000410
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0008844	decreased subcutaneous adipose tissue amount	CCO:MP0008844
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0003853	dry skin	CCO:MP0003853
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0003704	abnormal hair follicle development	CCO:MP0003704
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0003290	hypoperistalsis	CCO:MP0003290
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0005150	cachexia	CCO:MP0005150
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001951	abnormal breathing	CCO:MP0001951
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001302	eyelids open at birth	CCO:MP0001302
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001199	thin skin	CCO:MP0001199
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001195	flaky skin	CCO:MP0001195
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0003819	increased left ventricle diastolic pressure	CCO:MP0003819
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001221	epidermal atrophy	CCO:MP0001221
MGI:99511	Ptpn11	Ptpn11<tm1Rbn>/Ptpn11<tm1Rbn>	involves: 129 * Black Swiss	MP:0001935	decreased litter size	CCO:MP0001935
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0000379	decreased hair follicle number	CCO:MP0000379
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0000383	abnormal hair follicle orientation	CCO:MP0000383
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001176	abnormal lung development	CCO:MP0001176
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0000377	abnormal hair follicle morphology	CCO:MP0000377
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0002108	abnormal muscle morphology	CCO:MP0002108
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0002073	abnormal hair growth	CCO:MP0002073
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0003896	prolonged PQ interval	CCO:MP0003896
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0003897	abnormal ST interval	CCO:MP0003897
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Paw>/Ptpn11<+>"	involves: 129S1/Sv * 129X1/SvJ * B6EiC3Sn a/A-Egfr<wa2> Wnt3a<vt> * C57BL/6	MP:0001218	thin epidermis	CCO:MP0001218
MGI:99511	Ptpn11	"Egfr<wa2>/Egfr<wa2>,Ptpn11<tm1Rbn>/Ptpn11<+>"	involves: 129 * B6EiC3Sn-a/A-Egfr<wa2> Wnt3a<vt>	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001675	abnormal ectoderm development	CCO:MP0001675
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001695	abnormal gastrulation	CCO:MP0001695
MGI:99511	Ptpn11	Ptpn11<tm1Paw>/Ptpn11<tm1Paw>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0005013	increased lymphocyte cell number	CCO:MP0005013
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0005352	small skull	CCO:MP0005352
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0003223	decreased cardiomyocyte apoptosis	CCO:MP0003223
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005479	decreased circulating triiodothyronine level	CCO:MP0005479
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0001654	hepatic necrosis	CCO:MP0001654
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000219	increased neutrophil cell number	CCO:MP0000219
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005669	increased circulating leptin level	CCO:MP0005669
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000286	abnormal mitral valve morphology	CCO:MP0000286
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005478	decreased circulating thyroxine level	CCO:MP0005478
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005534	decreased body temperature	CCO:MP0005534
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005455	increased weight gain	CCO:MP0005455
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000599	enlarged liver	CCO:MP0000599
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0001258	decreased body length	CCO:MP0001258
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0000601	small liver	CCO:MP0000601
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0001654	hepatic necrosis	CCO:MP0001654
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001257	increased body length	CCO:MP0001257
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0001914	hemorrhage	CCO:MP0001914
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0005312	pericardial effusion	CCO:MP0005312
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000008	increased white adipose tissue amount	CCO:MP0000008
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000005	increased brown adipose tissue amount	CCO:MP0000005
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002078	abnormal glucose homeostasis	CCO:MP0002078
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0002192	hydrops fetalis	CCO:MP0002192
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001552	increased circulating triglyceride level	CCO:MP0001552
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<+>	involves: 129S4/SvJae * C57BL/6J	MP:0000443	abnormal snout morphology	CCO:MP0000443
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:99511	Ptpn11	Ptpn11<tm1Bgn>/Ptpn11<tm1Bgn>	involves: 129S4/SvJae * C57BL/6J	MP:0003223	decreased cardiomyocyte apoptosis	CCO:MP0003223
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005440	increased glycogen level	CCO:MP0005440
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005418	abnormal circulating hormone level	CCO:MP0005418
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005317	increased triglyceride level	CCO:MP0005317
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005122	increased circulating thyroid-stimulating hormone level	CCO:MP0005122
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001261	obese	CCO:MP0001261
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001744	hypersecretion of corticosterone	CCO:MP0001744
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001745	increased circulating corticosterone level	CCO:MP0001745
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001559	hyperglycemia	CCO:MP0001559
MGI:99511	Ptpn11	"Ptpn11<tm1Gsf>/Ptpn11<tm1Gsf>,Tg(Camk2a-cre)2Szi/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005123	increased circulating growth hormone level	CCO:MP0005123
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0008215	decreased immature B cell number	CCO:MP0008215
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0001577	anemia	CCO:MP0001577
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0008211	decreased mature B cell number	CCO:MP0008211
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0001861	lung inflammation	CCO:MP0001861
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0008172	abnormal follicular B cell morphology	CCO:MP0008172
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0008188	abnormal transitional stage B cell morphology	CCO:MP0008188
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0002144	abnormal B cell differentiation	CCO:MP0002144
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0001601	abnormal myelopoiesis	CCO:MP0001601
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0002083	premature death	CCO:MP0002083
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	MP:0008172	abnormal follicular B cell morphology	CCO:MP0008172
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	MP:0003009	abnormal cytokine secretion	CCO:MP0003009
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	MP:0001798	impaired macrophage phagocytosis	CCO:MP0001798
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	MP:0002459	abnormal B cell physiology	CCO:MP0002459
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	MP:0001601	abnormal myelopoiesis	CCO:MP0001601
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	involves: 129P2/OlaHsd * BALB/cJ * C57BL/6	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:97810	Ptprc	"Ptprc<tm1Mak>/Ptprc<tm1Mak>,Ptprj<tm1.2Weis>/Ptprj<tm1.2Weis>"	B6.Cg-Ptprc<tm1Mak> Ptprj<tm1.2Weis>	MP:0001860	liver inflammation	CCO:MP0001860
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0008217	abnormal B cell activation	CCO:MP0008217
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0001828	abnormal T cell activation	CCO:MP0001828
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0001861	lung inflammation	CCO:MP0001861
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0002408	abnormal double-positive T cell morphology	CCO:MP0002408
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0005160	proteinuria	CCO:MP0005160
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0005264	glomerulosclerosis	CCO:MP0005264
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0003725	increased autoantibody level	CCO:MP0003725
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0003850	abnormal thymocyte activation	CCO:MP0003850
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0003944	abnormal T cell subpopulation ratio	CCO:MP0003944
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0004969	pale kidney	CCO:MP0004969
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0008049	increased memory T cell number	CCO:MP0008049
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0008097	increased plasma cell number	CCO:MP0008097
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0008174	decreased follicular B cell number	CCO:MP0008174
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0001828	abnormal T cell activation	CCO:MP0001828
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0003850	abnormal thymocyte activation	CCO:MP0003850
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0008217	abnormal B cell activation	CCO:MP0008217
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0008191	abnormal follicular B cell physiology	CCO:MP0008191
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0008189	increased transitional stage B cell number	CCO:MP0008189
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0008174	decreased follicular B cell number	CCO:MP0008174
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0008097	increased plasma cell number	CCO:MP0008097
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0008189	increased transitional stage B cell number	CCO:MP0008189
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0003944	abnormal T cell subpopulation ratio	CCO:MP0003944
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0008191	abnormal follicular B cell physiology	CCO:MP0008191
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0002408	abnormal double-positive T cell morphology	CCO:MP0002408
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0001861	lung inflammation	CCO:MP0001861
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0001828	abnormal T cell activation	CCO:MP0001828
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0001860	liver inflammation	CCO:MP0001860
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0000717	abnormal lymphocyte cell number	CCO:MP0000717
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	B6.129X1-Ptprc<tm1Weis>	MP:0008049	increased memory T cell number	CCO:MP0008049
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0000217	abnormal leukocyte cell number	CCO:MP0000217
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0005015	increased T cell number	CCO:MP0005015
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0005014	increased B cell number	CCO:MP0005014
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0002495	increased IgA level	CCO:MP0002495
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0002743	glomerulonephritis	CCO:MP0002743
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0005350	increased susceptibility to autoimmune disorder	CCO:MP0005350
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0001664	abnormal digestion	CCO:MP0001664
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<+>	involves: 129X1/SvJ * C57BL/6	MP:0008500	increased IgG2a level	CCO:MP0008500
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<+>	involves: 129X1/SvJ * C57BL/6	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<+>	involves: 129X1/SvJ * C57BL/6	MP:0002962	increased protein excretion	CCO:MP0002962
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<+>	involves: 129X1/SvJ * C57BL/6	MP:0005350	increased susceptibility to autoimmune disorder	CCO:MP0005350
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0008217	abnormal B cell activation	CCO:MP0008217
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<+>	involves: 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0001262	decreased body weight	CCO:MP0001262
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0002083	premature death	CCO:MP0002083
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0008524	increased plasmacytoid dendritic cell number	CCO:MP0008524
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0008500	increased IgG2a level	CCO:MP0008500
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0002722	abnormal immune system organ morphology	CCO:MP0002722
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0008476	increased spleen red pulp amount	CCO:MP0008476
MGI:97810	Ptprc	"Ptpn22<tm2Achn>/Ptpn22<tm2Achn>,Ptprc<tm1Weis>/Ptprc<tm1Weis>"	B6.Cg-Ptprc<tm1Weis> Ptpn22<tm2Achn>	MP:0001860	liver inflammation	CCO:MP0001860
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0008111	abnormal granulocyte differentiation	CCO:MP0008111
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0008102	lymph node hyperplasia	CCO:MP0008102
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0004762	increased anti-double stranded DNA antibody level	CCO:MP0004762
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0003620	decreased urine output	CCO:MP0003620
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0003606	kidney failure	CCO:MP0003606
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0002962	increased protein excretion	CCO:MP0002962
MGI:97810	Ptprc	Ptprc<tm1Weis>/Ptprc<tm1Weis>	involves: 129X1/SvJ * C57BL/6	MP:0008478	increased spleen white pulp amount	CCO:MP0008478
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:97810	Ptprc	"Ptprc<tm1Holm>/Ptprc<tm1Holm>,Tg(Lck*F505)3073Rmp/?"	involves: 129/Sv * C57BL/6 * DBA/2	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0002458	abnormal B cell number	CCO:MP0002458
MGI:97810	Ptprc	"Ptprc<tm1Holm>/Ptprc<tm1Holm>,Tg(Lck*F505)3073Rmp/?"	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:97810	Ptprc	"Ptprc<tm1Holm>/Ptprc<tm1Holm>,Tg(Lck*F505)2964Rmp/?"	involves: 129/Sv * C57BL/6 * DBA/2	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:97810	Ptprc	"Ptprc<tm1Holm>/Ptprc<tm1Holm>,Tg(Lck*F505)2964Rmp/?"	involves: 129/Sv * C57BL/6 * DBA/2	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:97810	Ptprc	Ptprc<tm1Holm>/Ptprc<tm1Holm>	involves: 129/Sv * C57BL/6	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0001823	thymus hypoplasia	CCO:MP0001823
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	involves: 129S2/SvPas * C57BL/6 * DBA/2	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	129S2/SvPas-Ptprc<tm1Tyb>	MP:0005036	diarrhea	CCO:MP0005036
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	129S2/SvPas-Ptprc<tm1Tyb>	MP:0008569	lethality at weaning	CCO:MP0008569
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0003850	abnormal thymocyte activation	CCO:MP0003850
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0004917	abnormal T cell selection	CCO:MP0004917
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0008037	abnormal T cell morphology	CCO:MP0008037
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0002444	abnormal T cell physiology	CCO:MP0002444
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	B6.129S2-Ptprc<tm1Tyb>	MP:0008044	increased NK cell number	CCO:MP0008044
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0004919	abnormal positive T cell selection	CCO:MP0004919
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0002145	abnormal T cell differentiation	CCO:MP0002145
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0008048	abnormal memory T cell number	CCO:MP0008048
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0005090	increased double-negative T cell number	CCO:MP0005090
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	B6.129S2-Ptprc<tm1Tyb>	MP:0005069	abnormal NK cell physiology	CCO:MP0005069
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	B6.129S2-Ptprc<tm1Tyb>	MP:0002526	abnormal chemokine physiology	CCO:MP0002526
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	C.129S2-Ptprc<tm1Tyb>	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:97810	Ptprc	Ptprc<tm1Tyb>/Ptprc<tm1Tyb>	B6.129S2-Ptprc<tm1Tyb>	MP:0003009	abnormal cytokine secretion	CCO:MP0003009
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0001825	arrested T cell differentiation	CCO:MP0001825
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0005092	decreased double-positive T cell number	CCO:MP0005092
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0002458	abnormal B cell number	CCO:MP0002458
MGI:97810	Ptprc	Ptprc<loc>/Ptprc<loc>	C57BL/6Apb-Ptprc<loc>/Apb	MP:0002408	abnormal double-positive T cell morphology	CCO:MP0002408
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0004185	abnormal adipocyte glucose uptake	CCO:MP0004185
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0002644	decreased circulating triglyceride level	CCO:MP0002644
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0002702	decreased circulating free fatty acid level	CCO:MP0002702
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0004889	increased energy expenditure	CCO:MP0004889
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0005217	abnormal pancreatic beta cell morphology	CCO:MP0005217
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0004892	increased adiponectin level	CCO:MP0004892
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0009283	decreased gonadal fat pad weight	CCO:MP0009283
MGI:108027	Ptprv	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0002891	increased insulin sensitivity	CCO:MP0002891
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0005491	pancreatic islet hyperplasia	CCO:MP0005491
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0003058	increased insulin secretion	CCO:MP0003058
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0006035	abnormal mitochondrial morphology	CCO:MP0006035
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0006094	increased fat cell size	CCO:MP0006094
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:108027	Ptprv	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	MP:0005659	increased resistance to diet-induced obesity	CCO:MP0005659
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:108027	Ptprv	Ptprv<tm1Asmi>/Ptprv<tm1Asmi>	involves: 129P2/OlaHsd	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0004130	abnormal muscle cell glucose uptake	CCO:MP0004130
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0005292	improved glucose tolerance	CCO:MP0005292
MGI:108027	Ptprv	"Ptprv<tm1Kry>/Ptprv<tm1Kry>,Tg(Col1a1-cre)1Kry/?"	involves: FVB	MP:0002078	abnormal glucose homeostasis	CCO:MP0002078
MGI:108027	Ptprv	"Lep<ob>/Lep<ob>,Ptprv<tm1Asmi>/Ptprv<+>"	involves: 129P2/OlaHsd * STOCK Mlph<ln> a Tgfa<wa1> Cdh23<v> Ednrb<s>	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:108027	Ptprv	"Lep<ob>/Lep<ob>,Ptprv<tm1Asmi>/Ptprv<tm1Asmi>"	involves: 129P2/OlaHsd * STOCK Mlph<ln> a Tgfa<wa1> Cdh23<v> Ednrb<s>	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:108027	Ptprv	"Lep<ob>/Lep<ob>,Ptprv<tm1Asmi>/Ptprv<tm1Asmi>"	involves: 129P2/OlaHsd * STOCK Mlph<ln> a Tgfa<wa1> Cdh23<v> Ednrb<s>	MP:0005292	improved glucose tolerance	CCO:MP0005292
MGI:108027	Ptprv	"Lep<ob>/Lep<ob>,Ptprv<tm1Asmi>/Ptprv<tm1Asmi>"	involves: 129P2/OlaHsd * STOCK Mlph<ln> a Tgfa<wa1> Cdh23<v> Ednrb<s>	MP:0002079	increased circulating insulin level	CCO:MP0002079
MGI:108027	Ptprv	Ptprv<tm1Asmi>/Ptprv<+>	involves: 129P2/OlaHsd * MF1	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1353578	Pttg1	"Espl1<tm1.2Tno>/Espl1<+>,Pttg1<tm1Tno>/Pttg1<tm1Tno>"	involves: 129S4/SvJae * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1353578	Pttg1	"Cdc20<Gt(XE368)Byg>/Cdc20<Gt(XE368)Byg>,Pttg1<tm1Pzg>/Pttg1<tm1Pzg>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:1353578	Pttg1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:1353578	Pttg1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1353578	Pttg1	Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>	involves: 129P2/OlaHsd * C57BL/6	MP:0001921	reduced fertility	CCO:MP0001921
MGI:1353578	Pttg1	"Espl1<tm1.2Tno>/Espl1<+>,Pttg1<tm1Tno>/Pttg1<tm1Tno>"	involves: 129S4/SvJae * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1353578	Pttg1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:1353578	Pttg1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:1353578	Pttg1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1353578	Pttg1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0003111	abnormal nucleus morphology	CCO:MP0003111
MGI:1353578	Pttg1	"Espl1<tm1.2Kna>/Espl1<+>,Pttg1<tm1.2Kna>/Pttg1<tm1.2Kna>"	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1353578	Pttg1	Pttg1<tm1Pzg>/Pttg1<tm1Pzg>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1353578	Pttg1	Pttg1<tm1Pzg>/Pttg1<tm1Pzg>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1353578	Pttg1	"Cdc20<Gt(XE368)Byg>/Cdc20<Gt(XE368)Byg>,Pttg1<tm1Pzg>/Pttg1<tm1Pzg>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1353578	Pttg1	"Espl1<tm1.1Tno>/Espl1<+>,Pttg1<tm1Tno>/Pttg1<tm1Tno>"	involves: 129S4/SvJae * C57BL/6J	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0002722	abnormal immune system organ morphology	CCO:MP0002722
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0005015	increased T cell number	CCO:MP0005015
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0002727	decreased circulating insulin level	CCO:MP0002727
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0005217	abnormal pancreatic beta cell morphology	CCO:MP0005217
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0001805	decreased IgG level	CCO:MP0001805
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0005449	abnormal food intake	CCO:MP0005449
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0004953	decreased spleen weight	CCO:MP0004953
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0001806	decreased IgM level	CCO:MP0001806
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0001762	polyuria	CCO:MP0001762
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0002460	decreased immunoglobulin level	CCO:MP0002460
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0001559	hyperglycemia	CCO:MP0001559
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0001935	decreased litter size	CCO:MP0001935
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0005606	increased bleeding time	CCO:MP0005606
MGI:1353578	Pttg1	Pttg1<tm1Sme>/Pttg1<tm1Sme>	involves: 129S4/SvJae * C57BL/6	MP:0006319	abnormal epididymal fat pad morphology	CCO:MP0006319
MGI:1349423	Racgap1	"Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0008190	decreased transitional stage B cell number	CCO:MP0008190
MGI:1349423	Racgap1	"Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:1349423	Racgap1	"Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0001601	abnormal myelopoiesis	CCO:MP0001601
MGI:1349423	Racgap1	"Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1349423	Racgap1	"Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:1349423	Racgap1	"Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:1349423	Racgap1	"Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0008208	decreased pro-B cell number	CCO:MP0008208
MGI:1349423	Racgap1	"Racgap1<tm1Mahi>/Racgap1<tm1Mahi>,Tg(Mx1-cre)1Cgn/0"	involves: C57BL/6 * CBA	MP:0002144	abnormal B cell differentiation	CCO:MP0002144
MGI:1349423	Racgap1	Racgap1<Gt(pSABetageo)11Huy>/Racgap1<Gt(pSABetageo)11Huy>	involves: 129X1/SvJ * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1349423	Racgap1	Racgap1<Gt(pSABetageo)11Huy>/Racgap1<Gt(pSABetageo)11Huy>	involves: 129X1/SvJ * C57BL/6	MP:0003406	failure of zygotic cell division	CCO:MP0003406
MGI:1349423	Racgap1	Racgap1<Gt(pSABetageo)11Huy>/Racgap1<Gt(pSABetageo)11Huy>	involves: 129X1/SvJ * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1333807	Rad17	Rad17<tm1Maas>/Rad17<tm1Maas>	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1333807	Rad17	Rad17<tm1Maas>/Rad17<tm1Maas>	involves: 129P2/OlaHsd * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:1333807	Rad17	Rad17<tm1Maas>/Rad17<tm1Maas>	involves: 129P2/OlaHsd * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1333807	Rad17	Rad17<tm1Maas>/Rad17<tm1Maas>	involves: 129P2/OlaHsd * C57BL/6	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:1333807	Rad17	Rad17<tm1Maas>/Rad17<tm1Maas>	involves: 129P2/OlaHsd * C57BL/6	MP:0001689	incomplete somite formation	CCO:MP0001689
MGI:1333807	Rad17	Rad17<tm1Maas>/Rad17<tm1Maas>	involves: 129P2/OlaHsd * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1333807	Rad17	Rad17<tm1Maas>/Rad17<tm1Maas>	involves: 129P2/OlaHsd * C57BL/6	MP:0002884	abnormal branchial arch morphology	CCO:MP0002884
MGI:109292	Rad50	"Nbn<tm2.1Jpt>/Nbn<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * 129/Sv	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:109292	Rad50	"Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * 129/Sv	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Rad50<tm1Jpt>/Rad50<tm3Jpt>,Tg(Pcp2-cre)2Mpin/0"	involves: 129/Sv * C57BL/6	MP:0001406	abnormal gait	CCO:MP0001406
MGI:109292	Rad50	"Rad50<tm1Jpt>/Rad50<tm3Jpt>,Tg(Mx1-cre)1Cgn/0"	involves: 129/Sv * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0004001	decreased hepatocyte proliferation	CCO:MP0004001
MGI:109292	Rad50	"Rad50<tm1Jpt>/Rad50<tm3Jpt>,Tg(Mx1-cre)1Cgn/0"	involves: 129/Sv * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	"Nbn<tm2.1Jpt>/Nbn<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * 129/Sv	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Nbn<tm2.1Jpt>/Nbn<tm2.1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * 129/Sv	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:109292	Rad50	"Rad50<tm1Jpt>/Rad50<tm3Jpt>,Tg(Mx1-cre)1Cgn/0"	involves: 129/Sv * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Rad50<tm1Jpt>/Rad50<tm3Jpt>,Tg(Mx1-cre)1Cgn/0"	involves: 129/Sv * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0003134	increased late pro-B cell number	CCO:MP0003134
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0005425	increased macrophage cell number	CCO:MP0005425
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0008209	decreased pre-B cell number	CCO:MP0008209
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0000703	abnormal thymus morphology	CCO:MP0000703
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0008215	decreased immature B cell number	CCO:MP0008215
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0000716	abnormal immune system cell morphology	CCO:MP0000716
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0002722	abnormal immune system organ morphology	CCO:MP0002722
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0002026	leukemia	CCO:MP0002026
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0001606	impaired hematopoiesis	CCO:MP0001606
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0000175	absent bone marrow cell	CCO:MP0000175
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6)	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0005432	abnormal pro-B cell morphology	CCO:MP0005432
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000237	decreased blood cell number	CCO:MP0000237
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008208	decreased pro-B cell number	CCO:MP0008208
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002396	abnormal hematopoietic system morphology/development	CCO:MP0002396
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Tg(BCL2)22Wehi/0"	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6JWehi * SJL/JWehi	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Tg(BCL2)22Wehi/0"	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6JWehi * SJL/JWehi	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Chek2<tm1Mak>/Chek2<tm1Mak>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	"Chek2<tm1Mak>/Chek2<tm1Mak>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:109292	Rad50	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:109292	Rad50	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0005432	abnormal pro-B cell morphology	CCO:MP0005432
MGI:109292	Rad50	"Chek2<tm1Mak>/Chek2<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:109292	Rad50	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0002396	abnormal hematopoietic system morphology/development	CCO:MP0002396
MGI:109292	Rad50	"Mre11a<tm1Jpt>/Mre11a<tm1Jpt>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:109292	Rad50	Rad50<tm1Flv>/Rad50<tm1Flv>	involves: 129S6/SvEvTac * C57BL/6	MP:0002529	abnormal interleukin physiology	CCO:MP0002529
MGI:109292	Rad50	Rad50<tm1Flv>/Rad50<tm1Flv>	involves: 129S6/SvEvTac * C57BL/6	MP:0005466	abnormal T-helper 2 physiology	CCO:MP0005466
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001545	abnormal hematopoietic system physiology	CCO:MP0001545
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<tm1Awb>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:109292	Rad50	Rad50<tm1Jpt>/Rad50<tm1Jpt>	involves: 129S7/SvEvBrd	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:109292	Rad50	Rad50<tm2Jpt>/Rad50<tm2Jpt>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:109292	Rad50	"Atm<tm1Awb>/Atm<+>,Rad50<tm2Jpt>/Rad50<tm2Jpt>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:97890	Rad51	"Rad51<tm1Hst>/Rad51<tm1Hst>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:97890	Rad51	"Rad51<tm1Hst>/Rad51<tm1Hst>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:97890	Rad51	Rad51<tm1Hst>/Rad51<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:97890	Rad51	Rad51<tm1Hst>/Rad51<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:97890	Rad51	Rad51<tm1Hst>/Rad51<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:97890	Rad51	Rad51<tm1Hst>/Rad51<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:97890	Rad51	Rad51<tm1Hst>/Rad51<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001683	absent mesoderm	CCO:MP0001683
MGI:97890	Rad51	Rad51<tm1Hst>/Rad51<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:97890	Rad51	Rad51<tm1Hst>/Rad51<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:97890	Rad51	Rad51<tm1Hst>/Rad51<tm1Hst>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:97890	Rad51	Rad51<tm1Tkm>/Rad51<tm1Tkm>	involves: 129S/SvEv	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001919	abnormal reproductive system physiology	CCO:MP0001919
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<+>	involves: 129/Sv * C57BL/6J	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:2150020	Rad51c	Rad51c<tm1.1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001926	female infertility	CCO:MP0001926
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001925	male infertility	CCO:MP0001925
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001134	absent corpus luteum	CCO:MP0001134
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001924	infertility	CCO:MP0001924
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:2150020	Rad51c	Rad51c<tm1Sks>/Rad51c<tm1.1Sks>	involves: 129/Sv * C57BL/6J * FVB/N	MP:0001935	decreased litter size	CCO:MP0001935
MGI:1328356	Rad9	"Rad9<tm2Lieb>/Rad9<tm2Lieb>,Tg(KRT5-cre)1Xya/?"	involves: 129S/SvEv * C57BL/6	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1328356	Rad9	"Rad9<tm2Lieb>/Rad9<tm2Lieb>,Tg(KRT5-cre)1Xya/?"	involves: 129S/SvEv * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:1328356	Rad9	"Rad9<tm2Lieb>/Rad9<+>,Tg(KRT5-cre)1Xya/?"	involves: 129S/SvEv * C57BL/6	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1328356	Rad9	"Rad9<tm2Lieb>/Rad9<tm2Lieb>,Tg(KRT5-cre)1Xya/?"	involves: 129S/SvEv * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1328356	Rad9	"Rad9<tm2Lieb>/Rad9<tm2Lieb>,Tg(KRT5-cre)1Xya/?"	involves: 129S/SvEv * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1328356	Rad9	"Rad9<tm2Lieb>/Rad9<tm2Lieb>,Tg(KRT5-cre)1Xya/?"	involves: 129S/SvEv * C57BL/6	MP:0002095	abnormal skin pigmentation	CCO:MP0002095
MGI:1328356	Rad9	"Rad9<tm2Lieb>/Rad9<+>,Tg(KRT5-cre)1Xya/?"	involves: 129S/SvEv * C57BL/6	MP:0002095	abnormal skin pigmentation	CCO:MP0002095
MGI:1328356	Rad9	"Rad9<tm2Lieb>/Rad9<+>,Tg(KRT5-cre)1Xya/?"	involves: 129S/SvEv * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:1328356	Rad9	Rad9<tm1Lieb>/Rad9<tm1Lieb>	involves: 129S/SvEv * Black Swiss	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1328356	Rad9	Rad9<tm1Lieb>/Rad9<tm1Lieb>	involves: 129S/SvEv * Black Swiss	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1328356	Rad9	Rad9<tm1Lieb>/Rad9<tm1Lieb>	involves: 129S/SvEv * Black Swiss	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0001522	impaired swimming	CCO:MP0001522
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0004362	cochlear hair cell degeneration	CCO:MP0004362
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0002623	abnormal vestibular hair cell morphology	CCO:MP0002623
MGI:97874	Rb1	Rb1<tm1.2Gfk>/Rb1<+>	involves: 129T2/SvEms * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	Rb1<tm1.2Gfk>/Rb1<+>	involves: 129T2/SvEms * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	Rb1<tm1Fad>/Rb1<tm1Fad>	involves: 129 * C57BL/6	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:97874	Rb1	Rb1<tm1Fad>/Rb1<tm1Fad>	involves: 129 * C57BL/6	MP:0004024	aneuploidy	CCO:MP0004024
MGI:97874	Rb1	"Rb1<tm1Brd>/Rb1<+>,Snrpn<tm4Alb>/Snrpn<+>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0003787	abnormal imprinting	CCO:MP0003787
MGI:97874	Rb1	"Rb1<tm1Dwg>/Rb1<tm2Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129/Sv * C57BL/6 * SJL	MP:0006068	abnormal horizontal cell morphology	CCO:MP0006068
MGI:97874	Rb1	Rb1<tm1Fad>/Rb1<tm1Fad>	involves: 129 * C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0001394	circling	CCO:MP0001394
MGI:97874	Rb1	"Rb1<tm1Brd>/Rb1<+>,Snrpn<tm4Alb>/Snrpn<+>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0008877	abnormal DNA methylation	CCO:MP0008877
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0004324	vestibular hair cell degeneration	CCO:MP0004324
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0000042	abnormal organ of Corti	CCO:MP0000042
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0001967	deafness	CCO:MP0001967
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0004399	abnormal cochlear outer hair cell morphology	CCO:MP0004399
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0004401	increased cochlear outer hair cell number	CCO:MP0004401
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0004404	cochlear outer hair cell degeneration	CCO:MP0004404
MGI:97874	Rb1	"Rb1<tm1.1Gfk>/Rb1<tm1.1Gfk>,Tg(Tyr-cre)1Gfk/0"	involves: 129T2/SvEms * C57BL/6 * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0002622	abnormal cochlear hair cell morphology	CCO:MP0002622
MGI:97874	Rb1	"Rb1<tm1Dwg>/Rb1<tm2Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129/Sv * C57BL/6 * SJL	MP:0008453	decreased retinal rod cell number	CCO:MP0008453
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0008306	abnormal supporting cell proliferation	CCO:MP0008306
MGI:97874	Rb1	"Rb1<tm1.1Gfk>/Rb1<tm1.1Gfk>,Tg(Tyr-cre)1Gfk/0"	involves: 129T2/SvEms * C57BL/6 * SJL	MP:0002877	abnormal melanocyte morphology	CCO:MP0002877
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pou4f3-cre)1Zyc/0"	involves: 129S/SvEv	MP:0002979	abnormal vestibular response	CCO:MP0002979
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * FVB/N	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0006005	decreased interneuron number	CCO:MP0006005
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000873	thin external granule cell layer	CCO:MP0000873
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000872	abnormal external granule cell layer morphology	CCO:MP0000872
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Pcp2-cre)756Mro/0"	involves: 129P2/OlaHsd * FVB	MP:0000864	abnormal vermis morphology	CCO:MP0000864
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004097	abnormal cerebellar cortex morphology	CCO:MP0004097
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * FVB/N	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0008446	decreased retinal cone cell number	CCO:MP0008446
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006096	absent retinal bipolar cells	CCO:MP0006096
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006069	abnormal retinal neuronal layer morphology	CCO:MP0006069
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000890	thin cerebellar molecular layer	CCO:MP0000890
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pcp2-cre)756Mro/0"	involves: 129P2/OlaHsd * FVB	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004948	abnormal neuronal precursor proliferation	CCO:MP0004948
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000851	cerebellum hypoplasia	CCO:MP0000851
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000864	abnormal vermis morphology	CCO:MP0000864
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0001393	ataxia	CCO:MP0001393
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004097	abnormal cerebellar cortex morphology	CCO:MP0004097
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0003354	astrocytosis	CCO:MP0003354
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000864	abnormal vermis morphology	CCO:MP0000864
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0001393	ataxia	CCO:MP0001393
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004948	abnormal neuronal precursor proliferation	CCO:MP0004948
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004098	abnormal granule neuron	CCO:MP0004098
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0005240	abnormal amacrine cell morphology	CCO:MP0005240
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004948	abnormal neuronal precursor proliferation	CCO:MP0004948
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006068	abnormal horizontal cell morphology	CCO:MP0006068
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004174	abnormal spine curvature	CCO:MP0004174
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004025	polyploidy	CCO:MP0004025
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0003084	abnormal skeletal muscle fiber morphology	CCO:MP0003084
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004333	abnormal utricular macula morphology	CCO:MP0004333
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0002623	abnormal vestibular hair cell morphology	CCO:MP0002623
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0000042	abnormal organ of Corti	CCO:MP0000042
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0000759	abnormal skeletal muscle morphology	CCO:MP0000759
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0001505	hunched posture	CCO:MP0001505
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0000729	abnormal myogenesis	CCO:MP0000729
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0001388	abnormal stationary movement	CCO:MP0001388
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0009408	decreased skeletal muscle fiber density	CCO:MP0009408
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0008068	absent retinal ganglion cell	CCO:MP0008068
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	Rb1<tm1.2Gfk>/Rb1<tm1.2Gfk>	involves: 129T2/SvEms * C57BL/6 * SJL	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97874	Rb1	"Apaf1<tm1Mak>/Apaf1<tm1Mak>,Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0004407	increased cochlear hair cell number	CCO:MP0004407
MGI:97874	Rb1	"Apaf1<tm1Mak>/Apaf1<tm1Mak>,Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0004327	increased vestibular hair cell number	CCO:MP0004327
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004327	increased vestibular hair cell number	CCO:MP0004327
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0004327	increased vestibular hair cell number	CCO:MP0004327
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004819	decreased skeletal muscle mass	CCO:MP0004819
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004760	increased mitotic index	CCO:MP0004760
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004515	abnormal vestibular hair cell stereociliary bundle morphology	CCO:MP0004515
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004498	increased supporting cell number	CCO:MP0004498
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004407	increased cochlear hair cell number	CCO:MP0004407
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * C57BL/6	MP:0004401	increased cochlear outer hair cell number	CCO:MP0004401
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Tg(Rb1)#Blg/0"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0004407	increased cochlear hair cell number	CCO:MP0004407
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0001954	respiratory distress	CCO:MP0001954
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0002753	dilated heart left ventricle	CCO:MP0002753
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0005333	decreased heart rate	CCO:MP0005333
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0001785	edema	CCO:MP0001785
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0005598	decreased ventricle muscle contractility	CCO:MP0005598
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: FVB	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005205	abnormal eye anterior chamber	CCO:MP0005205
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005205	abnormal eye anterior chamber	CCO:MP0005205
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0004564	enlarged myocardial fiber	CCO:MP0004564
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0000274	enlarged heart	CCO:MP0000274
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0004215	abnormal myocardial fiber physiology	CCO:MP0004215
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001327	decreased retinal photoreceptor cell number	CCO:MP0001327
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Tg(S100b-v-erbB)4496Waw/0"	involves: 129S2/SvPas * C57BL/6J * DBA/2J * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Gfap-cre)2Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:97874	Rb1	"Rb1<tm1Brd>/Rb1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0001393	ataxia	CCO:MP0001393
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0001406	abnormal gait	CCO:MP0001406
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0001525	impaired balance	CCO:MP0001525
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0001394	circling	CCO:MP0001394
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0000745	tremors	CCO:MP0000745
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<+>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0001492	piloerection	CCO:MP0001492
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<+>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<+>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0004179	transmission ratio distortion	CCO:MP0004179
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<+>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002627	teratoma	CCO:MP0002627
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0001327	decreased retinal photoreceptor cell number	CCO:MP0001327
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0001327	decreased retinal photoreceptor cell number	CCO:MP0001327
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0004478	testicular teratoma	CCO:MP0004478
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<+>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0001492	piloerection	CCO:MP0001492
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0008515	thin retinal outer nuclear layer	CCO:MP0008515
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0008512	disorganized retinal inner nuclear layer	CCO:MP0008512
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0004179	transmission ratio distortion	CCO:MP0004179
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0003733	abnormal retinal inner nuclear layer morphology	CCO:MP0003733
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<+>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0005202	lethargy	CCO:MP0005202
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0005241	abnormal retinal ganglion layer morphology	CCO:MP0005241
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<+>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<+>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0005202	lethargy	CCO:MP0005202
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0008515	thin retinal outer nuclear layer	CCO:MP0008515
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<+>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<+>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0000512	intestinal ulcer	CCO:MP0000512
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0001263	weight loss	CCO:MP0001263
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0008515	thin retinal outer nuclear layer	CCO:MP0008515
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0008513	thin retinal inner plexiform layer	CCO:MP0008513
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0008511	thin retinal inner nuclear layer	CCO:MP0008511
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0003734	abnormal retinal inner plexiform layer morphology	CCO:MP0003734
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0003733	abnormal retinal inner nuclear layer morphology	CCO:MP0003733
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<tm1Brd>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0006096	absent retinal bipolar cells	CCO:MP0006096
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0009320	lymphoblastic lymphoma	CCO:MP0009320
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97874	Rb1	"Msh2<tm1Whl>/Msh2<tm1Whl>,Rb1<tm1Brd>/Rb1<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J	MP:0005276	skin tumor	CCO:MP0005276
MGI:97874	Rb1	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002022	lymphoma	CCO:MP0002022
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	Not Specified	MP:0002183	gliosis	CCO:MP0002183
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<+>	involves: 129S2/SvPas * C57BL/6J	MP:0008014	lung tumor	CCO:MP0008014
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0004898	uterine hemorrhage	CCO:MP0004898
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0008301	adrenal medulla hyperplasia	CCO:MP0008301
MGI:97874	Rb1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0009153	pancreas tumor	CCO:MP0009153
MGI:97874	Rb1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0008014	lung tumor	CCO:MP0008014
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<+>	involves: 129S2/SvPas * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"Kras<tm4Tyj>/Kras<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>"	Not Specified	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002947	hemangioma	CCO:MP0002947
MGI:97874	Rb1	"Kras<tm4Tyj>/Kras<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>"	Not Specified	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:97874	Rb1	"Kras<tm4Tyj>/Kras<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>"	Not Specified	MP:0002267	abnormal bronchiole morphology	CCO:MP0002267
MGI:97874	Rb1	"Kras<tm4Tyj>/Kras<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>"	Not Specified	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:97874	Rb1	"Kras<tm4Tyj>/Kras<+>,Rb1<tm3Tyj>/Rb1<tm3Tyj>"	Not Specified	MP:0008014	lung tumor	CCO:MP0008014
MGI:97874	Rb1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0003496	thyroid adenoma	CCO:MP0003496
MGI:97874	Rb1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0003495	parathyroid adenoma	CCO:MP0003495
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<+>	involves: 129S2/SvPas * C57BL/6J	MP:0002050	pheochromocytoma	CCO:MP0002050
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(KRT14-cre)8Brn/0,Tg(KRT5-Akt1*)Jmpa/0"	involves: C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(KRT14-cre)8Brn/0,Tg(KRT5-Akt1*)Jmpa/0"	involves: C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0003745	abnormal mucosal lining of the mouth	CCO:MP0003745
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm2Tyj>	chimera involves: 129S2/SvPas * C57BL/6	MP:0002009	preneoplasia	CCO:MP0002009
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm2Tyj>	chimera involves: 129S2/SvPas * C57BL/6	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm2Tyj>	chimera involves: 129S2/SvPas * C57BL/6	MP:0001304	cataracts	CCO:MP0001304
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm2Tyj>	chimera involves: 129S2/SvPas * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm2Tyj>	chimera involves: 129S2/SvPas * C57BL/6	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm2Tyj>	chimera involves: 129S2/SvPas * C57BL/6	MP:0000885	ectopic Purkinje cell	CCO:MP0000885
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm2Tyj>	chimera involves: 129S2/SvPas * C57BL/6	MP:0005150	cachexia	CCO:MP0005150
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm2Tyj>	chimera involves: 129S2/SvPas * C57BL/6	MP:0006099	thin granule layer	CCO:MP0006099
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<+>	involves: 129S2/SvPas * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Men1<tm1.1Ctre>/Men1<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6J * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0000681	abnormal thyroid gland morphology	CCO:MP0000681
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<+>,Rb1<tm1Tyj>/Rb1<tm1Tyj>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<+>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<+>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<tm1Njd>,Rb1<tm1Tyj>/Rb1<tm1Tyj>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97874	Rb1	"E2f1<tm1Njd>/E2f1<+>,Rb1<tm1Tyj>/Rb1<+>"	either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6)	MP:0003496	thyroid adenoma	CCO:MP0003496
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Trp53<tm1Brd>/Trp53<+>,Tg(Rbp3-cre)1Brn/0"	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Rbp3-cre)1Brn/0"	involves: FVB/N	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<tm1Jyjw>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<tm1Jyjw>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<tm1Jyjw>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0001492	piloerection	CCO:MP0001492
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<tm1Jyjw>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0005202	lethargy	CCO:MP0005202
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<tm1Jyjw>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006087	increased body mass index	CCO:MP0006087
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0008796	increased lens fiber apoptosis	CCO:MP0008796
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0008113	abnormal macrophage differentiation	CCO:MP0008113
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0004265	abnormal placental transport	CCO:MP0004265
MGI:97874	Rb1	Rb1<tm1Jyjw>/Rb1<tm1Jyjw>	either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6)	MP:0001492	piloerection	CCO:MP0001492
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000160	kyphosis	CCO:MP0000160
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000606	decreased hepatocyte number	CCO:MP0000606
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000774	decreased brain size	CCO:MP0000774
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0005202	lethargy	CCO:MP0005202
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000964	small dorsal root ganglion	CCO:MP0000964
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008534	enlarged fourth ventricle	CCO:MP0008534
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000601	small liver	CCO:MP0000601
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000602	enlarged liver sinusoidal spaces	CCO:MP0000602
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:97874	Rb1	Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>	either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac)	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005150	cachexia	CCO:MP0005150
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0001092	abnormal trigeminal ganglion morphology	CCO:MP0001092
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001261	obese	CCO:MP0001261
MGI:97874	Rb1	Rb1<tm1Brd>/Rb1<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000631	abnormal neuroendocrine gland morphology	CCO:MP0000631
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0001606	impaired hematopoiesis	CCO:MP0001606
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0000828	abnormal fourth ventricle morphology	CCO:MP0000828
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0003717	pallor	CCO:MP0003717
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0005039	hypoxia	CCO:MP0005039
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas	MP:0000826	abnormal third ventricle morphology	CCO:MP0000826
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0009153	pancreas tumor	CCO:MP0009153
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002035	leiomyosarcoma	CCO:MP0002035
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000606	decreased hepatocyte number	CCO:MP0000606
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0008254	increased megakaryocyte cell number	CCO:MP0008254
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<+>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<+>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000432	abnormal head morphology	CCO:MP0000432
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0001601	abnormal myelopoiesis	CCO:MP0001601
MGI:97874	Rb1	"E2f4<tm1Lees>/E2f4<tm1Lees>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000829	dilated fourth ventricle	CCO:MP0000829
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002229	neurodegeneration	CCO:MP0002229
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000829	dilated fourth ventricle	CCO:MP0000829
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000798	abnormal frontal lobe morphology	CCO:MP0000798
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000602	enlarged liver sinusoidal spaces	CCO:MP0000602
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000432	abnormal head morphology	CCO:MP0000432
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0002594	low mean erythrocyte cell number	CCO:MP0002594
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0001787	pericardial edema	CCO:MP0001787
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0001786	skin edema	CCO:MP0001786
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0001505	hunched posture	CCO:MP0001505
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0000601	small liver	CCO:MP0000601
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0000163	abnormal cartilage morphology	CCO:MP0000163
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000798	abnormal frontal lobe morphology	CCO:MP0000798
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0001601	abnormal myelopoiesis	CCO:MP0001601
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000602	enlarged liver sinusoidal spaces	CCO:MP0000602
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000606	decreased hepatocyte number	CCO:MP0000606
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002229	neurodegeneration	CCO:MP0002229
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:97874	Rb1	Rb1<tm1Mlh>/Rb1<tm1Mlh>	either: 129P2/OlaHsd-Rb1<tm1Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0008254	increased megakaryocyte cell number	CCO:MP0008254
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3.1Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0001505	hunched posture	CCO:MP0001505
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3.1Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0000729	abnormal myogenesis	CCO:MP0000729
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0001716	abnormal placenta labyrinth morphology	CCO:MP0001716
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0002446	abnormal macrophage morphology	CCO:MP0002446
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0001092	abnormal trigeminal ganglion morphology	CCO:MP0001092
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3.1Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0002176	increased brain weight	CCO:MP0002176
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0000826	abnormal third ventricle morphology	CCO:MP0000826
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3.1Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0005238	increased brain size	CCO:MP0005238
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0004265	abnormal placental transport	CCO:MP0004265
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0008796	increased lens fiber apoptosis	CCO:MP0008796
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Tyj>	involves: 129/Sv * 129S2/SvPas * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Tyj>	involves: 129/Sv * 129S2/SvPas * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Tyj>	involves: 129/Sv * 129S2/SvPas * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Tyj>	involves: 129/Sv * 129S2/SvPas * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:97874	Rb1	Rb1<tm1Dwg>/Rb1<tm1Dwg>	involves: 129/Sv * C57BL/6	MP:0000828	abnormal fourth ventricle morphology	CCO:MP0000828
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(KRT14-cre)8Brn/0,Tg(KRT14-HPV16E7)2304Plam/0"	involves: 129 * C57BL/6 * FVB	MP:0001233	abnormal epidermis suprabasal layer morphology	CCO:MP0001233
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<+>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<+>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0000961	abnormal dorsal root ganglion morphology	CCO:MP0000961
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0001963	abnormal hearing physiology	CCO:MP0001963
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0000042	abnormal organ of Corti	CCO:MP0000042
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0004327	increased vestibular hair cell number	CCO:MP0004327
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0004395	increased cochlear inner hair cell number	CCO:MP0004395
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0004401	increased cochlear outer hair cell number	CCO:MP0004401
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0004407	increased cochlear hair cell number	CCO:MP0004407
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3.1Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0008306	abnormal supporting cell proliferation	CCO:MP0008306
MGI:97874	Rb1	Rb1<tm2Mlh>/Rb1<tm2Mlh>	either: 129P2/OlaHsd-Rb1<tm2Mlh> or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB)	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(KRT14-cre)8Brn/0,Tg(KRT14-HPV16E7)2304Plam/0"	involves: 129 * C57BL/6 * FVB	MP:0001222	epidermal hyperplasia	CCO:MP0001222
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(KRT14-cre)8Brn/0,Tg(KRT14-HPV16E7)2304Plam/0"	involves: 129 * C57BL/6 * FVB	MP:0001239	abnormal epidermis stratum granulosum morphology	CCO:MP0001239
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(KRT14-cre)8Brn/0"	involves: 129 * C57BL/6 * FVB	MP:0001233	abnormal epidermis suprabasal layer morphology	CCO:MP0001233
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(KRT14-cre)8Brn/0"	involves: 129 * C57BL/6 * FVB	MP:0001222	epidermal hyperplasia	CCO:MP0001222
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(KRT14-cre)8Brn/0"	involves: 129 * C57BL/6 * FVB	MP:0001239	abnormal epidermis stratum granulosum morphology	CCO:MP0001239
MGI:97874	Rb1	"Rb1<tm1Fad>/Rb1<+>,Tg(KRT14-HPV16E7)2304Plam/0"	involves: 129 * C57BL/6 * FVB	MP:0001233	abnormal epidermis suprabasal layer morphology	CCO:MP0001233
MGI:97874	Rb1	"Rb1<tm1Fad>/Rb1<tm1Fad>,Tg(KRT14-HPV16E7)2304Plam/0"	involves: 129 * C57BL/6 * FVB	MP:0001233	abnormal epidermis suprabasal layer morphology	CCO:MP0001233
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3.1Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3.1Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3.1Tyj>,Tg(Nes-cre)1Mrt/0"	Not Specified	MP:0005545	abnormal lens development	CCO:MP0005545
MGI:97874	Rb1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Col1a1-cre)1Bek/0"	Not Specified	MP:0004840	increased Deiters cell number	CCO:MP0004840
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003315	abnormal perineum morphology	CCO:MP0003315
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001144	vagina atresia	CCO:MP0001144
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001004	abnormal retinal photoreceptor morphology	CCO:MP0001004
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(KRT14-HPV16E7)2304Plam/0"	involves: 129 * C57BL/6 * FVB	MP:0001239	abnormal epidermis stratum granulosum morphology	CCO:MP0001239
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<+>	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"E2f4<tm1Lees>/E2f4<tm1Lees>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:97874	Rb1	"E2f4<tm1Lees>/E2f4<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Tg(KRT14-HPV16E7)2304Plam/0"	involves: 129 * C57BL/6 * FVB	MP:0001233	abnormal epidermis suprabasal layer morphology	CCO:MP0001233
MGI:97874	Rb1	"E2f4<tm1Lees>/E2f4<+>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0000245	abnormal erythropoiesis	CCO:MP0000245
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<+>	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	Rb1<tm1Tyj>/Rb1<+>	involves: 129S2/SvPas * C57BL/6	MP:0005150	cachexia	CCO:MP0005150
MGI:97874	Rb1	"E2f4<tm1Lees>/E2f4<tm1Lees>,Rb1<tm1Tyj>/Rb1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002406	increased susceptibility to infection	CCO:MP0002406
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001270	distended abdomen	CCO:MP0001270
MGI:97874	Rb1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0003888	liver hemorrhage	CCO:MP0003888
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0002753	dilated heart left ventricle	CCO:MP0002753
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0004056	abnormal myocardial compact layer morphology	CCO:MP0004056
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0003904	decreased cell mass	CCO:MP0003904
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0005294	abnormal heart ventricle morphology	CCO:MP0005294
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0002189	abnormal myocardial trabeculae morphology	CCO:MP0002189
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0003887	increased hepatocyte apoptosis	CCO:MP0003887
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0000608	dissociated hepatocytes	CCO:MP0000608
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0000606	decreased hepatocyte number	CCO:MP0000606
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0001785	edema	CCO:MP0001785
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0004067	abnormal ventricular trabeculae morphology	CCO:MP0004067
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0000280	thin ventricular wall	CCO:MP0000280
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0003717	pallor	CCO:MP0003717
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0006138	congestive heart failure	CCO:MP0006138
MGI:1341850	Rb1cc1	Rb1cc1<tm1.1Guan>/Rb1cc1<tm1.1Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0003103	liver degeneration	CCO:MP0003103
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0005329	abnormal cardiac muscle morphology	CCO:MP0005329
MGI:1341850	Rb1cc1	Rb1cc1<tm1.2Guan>/Rb1cc1<tm1.2Guan>	involves: 129P2/OlaHsd * C57BL/6	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:2442995	Rbbp8	Rbbp8<tm1Whl>/Rbbp8<tm1Whl>	Not Specified	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:2442995	Rbbp8	Rbbp8<tm1Whl>/Rbbp8<tm1Whl>	Not Specified	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:2442995	Rbbp8	Rbbp8<tm1Whl>/Rbbp8<tm1Whl>	Not Specified	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2442995	Rbbp8	Rbbp8<tm1Whl>/Rbbp8<+>	Not Specified	MP:0002083	premature death	CCO:MP0002083
MGI:2442995	Rbbp8	Rbbp8<tm1Whl>/Rbbp8<+>	Not Specified	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:2442995	Rbbp8	Rbbp8<tm1Whl>/Rbbp8<tm1Whl>	Not Specified	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:103300	Rbl1	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0005240	abnormal amacrine cell morphology	CCO:MP0005240
MGI:103300	Rbl1	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:103300	Rbl1	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:103300	Rbl1	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008453	decreased retinal rod cell number	CCO:MP0008453
MGI:103300	Rbl1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0004022	abnormal cone electrophysiology	CCO:MP0004022
MGI:103300	Rbl1	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008453	decreased retinal rod cell number	CCO:MP0008453
MGI:103300	Rbl1	"E2f1<tm1Meg>/E2f1<+>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:103300	Rbl1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001327	decreased retinal photoreceptor cell number	CCO:MP0001327
MGI:103300	Rbl1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0005240	abnormal amacrine cell morphology	CCO:MP0005240
MGI:103300	Rbl1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:103300	Rbl1	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:103300	Rbl1	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:103300	Rbl1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:103300	Rbl1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0003734	abnormal retinal inner plexiform layer morphology	CCO:MP0003734
MGI:103300	Rbl1	"E2f1<tm1Meg>/E2f1<tm1Meg>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008515	thin retinal outer nuclear layer	CCO:MP0008515
MGI:103300	Rbl1	"E2f3<tm1.1Gle>/E2f3<tm1.1Gle>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006309	decreased retinal ganglion cell number	CCO:MP0006309
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004948	abnormal neuronal precursor proliferation	CCO:MP0004948
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/?"	involves: 129 * C57BL/6 * FVB/N * NMRI * SJL	MP:0005240	abnormal amacrine cell morphology	CCO:MP0005240
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001330	abnormal optic nerve morphology	CCO:MP0001330
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0004022	abnormal cone electrophysiology	CCO:MP0004022
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000864	abnormal vermis morphology	CCO:MP0000864
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000890	thin cerebellar molecular layer	CCO:MP0000890
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005205	abnormal eye anterior chamber	CCO:MP0005205
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005205	abnormal eye anterior chamber	CCO:MP0005205
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0001393	ataxia	CCO:MP0001393
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0001393	ataxia	CCO:MP0001393
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000864	abnormal vermis morphology	CCO:MP0000864
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000851	cerebellum hypoplasia	CCO:MP0000851
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<+>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004948	abnormal neuronal precursor proliferation	CCO:MP0004948
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pcp2-cre)756Mro/0"	involves: 129P2/OlaHsd * FVB	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0004097	abnormal cerebellar cortex morphology	CCO:MP0004097
MGI:103300	Rbl1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * FVB/N	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0006073	abnormal retinal bipolar cell morphology	CCO:MP0006073
MGI:103300	Rbl1	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(En2-cre)22Alj/0"	involves: 129P2/OlaHsd	MP:0000877	abnormal Purkinje cell morphology	CCO:MP0000877
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0005240	abnormal amacrine cell morphology	CCO:MP0005240
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0003734	abnormal retinal inner plexiform layer morphology	CCO:MP0003734
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0004021	abnormal rod electrophysiology	CCO:MP0004021
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0003733	abnormal retinal inner nuclear layer morphology	CCO:MP0003733
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008453	decreased retinal rod cell number	CCO:MP0008453
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:103300	Rbl1	"Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0008515	thin retinal outer nuclear layer	CCO:MP0008515
MGI:103300	Rbl1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * FVB/N	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:103300	Rbl1	"E2f2<tm1Zubi>/E2f2<tm1Zubi>,Rbl1<tm1Htr>/Rbl1<tm1Htr>,Tg(Pax6-cre,GFP)2Pgr/?"	involves: 129 * C57BL/6 * FVB/N * NMRI	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:103300	Rbl1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:103300	Rbl1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:103300	Rbl1	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:103300	Rbl1	Rbl1<tm1Tyj>/Rbl1<+>	involves: 129S2/SvPas * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:103300	Rbl1	Rbl1<tm1Tyj>/Rbl1<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003055	abnormal long bone epiphyseal plate morphology	CCO:MP0003055
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000445	short snout	CCO:MP0000445
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0005358	abnormal incisor morphology	CCO:MP0005358
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003408	increased width of hypertrophic chondrocyte zone	CCO:MP0003408
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000427	abnormal hair cycle	CCO:MP0000427
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001239	abnormal epidermis stratum granulosum morphology	CCO:MP0001239
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000402	abnormal zigzag hairs	CCO:MP0000402
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000397	abnormal guard hair	CCO:MP0000397
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000400	abnormal awl hair	CCO:MP0000400
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004359	short ulna	CCO:MP0004359
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000379	decreased hair follicle number	CCO:MP0000379
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004624	abnormal thoracic cage	CCO:MP0004624
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000383	abnormal hair follicle orientation	CCO:MP0000383
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004351	short humerus	CCO:MP0004351
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003427	parakeratosis	CCO:MP0003427
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0008160	increased diameter of humerus	CCO:MP0008160
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000125	absent incisors	CCO:MP0000125
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000382	underdeveloped hair follicles	CCO:MP0000382
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001951	abnormal breathing	CCO:MP0001951
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001957	apnea	CCO:MP0001957
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003704	abnormal hair follicle development	CCO:MP0003704
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000078	abnormal supraoccipital bone morphology	CCO:MP0000078
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003419	delayed endochondral bone ossification	CCO:MP0003419
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002656	abnormal keratinocyte differentiation	CCO:MP0002656
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000547	short limbs	CCO:MP0000547
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0005296	abnormal humerus morphology	CCO:MP0005296
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003662	abnormal long bone epiphyseal plate proliferative zone	CCO:MP0003662
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002823	abnormal rib development	CCO:MP0002823
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001222	epidermal hyperplasia	CCO:MP0001222
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000077	abnormal interparietal bone morphology	CCO:MP0000077
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004355	short radius	CCO:MP0004355
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003315	abnormal perineum morphology	CCO:MP0003315
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002683	delayed fertility	CCO:MP0002683
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001144	vagina atresia	CCO:MP0001144
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001004	abnormal retinal photoreceptor morphology	CCO:MP0001004
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001270	distended abdomen	CCO:MP0001270
MGI:103300	Rbl1	Rbl1<tm1Tyj>/Rbl1<tm1Tyj>	129/Sv	MP:0008151	increased diameter of long bones	CCO:MP0008151
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003120	abnormal tracheal cartilage morphology	CCO:MP0003120
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0008161	increased diameter of radius	CCO:MP0008161
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000116	abnormal tooth development	CCO:MP0000116
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0008163	increased diameter of ulna	CCO:MP0008163
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000652	enlarged sebaceous gland	CCO:MP0000652
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0008218	delayed emergence of vibrissae	CCO:MP0008218
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<+>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0001270	distended abdomen	CCO:MP0001270
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000547	short limbs	CCO:MP0000547
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001270	distended abdomen	CCO:MP0001270
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<+>,Rbl1<tm1Tyj>/Rbl1<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000445	short snout	CCO:MP0000445
MGI:103300	Rbl1	"Rb1<tm1Tyj>/Rb1<tm1Tyj>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:103300	Rbl1	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002116	abnormal craniofacial bone morphology	CCO:MP0002116
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006069	abnormal retinal neuronal layer morphology	CCO:MP0006069
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0002083	premature death	CCO:MP0002083
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0000274	enlarged heart	CCO:MP0000274
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006068	abnormal horizontal cell morphology	CCO:MP0006068
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0008068	absent retinal ganglion cell	CCO:MP0008068
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0001785	edema	CCO:MP0001785
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0005240	abnormal amacrine cell morphology	CCO:MP0005240
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0005333	decreased heart rate	CCO:MP0005333
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0008446	decreased retinal cone cell number	CCO:MP0008446
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0004564	enlarged myocardial fiber	CCO:MP0004564
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0005598	decreased ventricle muscle contractility	CCO:MP0005598
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0002753	dilated heart left ventricle	CCO:MP0002753
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0001954	respiratory distress	CCO:MP0001954
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006096	absent retinal bipolar cells	CCO:MP0006096
MGI:105085	Rbl2	"Rb1<tm2Brn>/Rb1<tm2Brn>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Myh6-cre)2182Mds/Tg(Myh6-cre)2182Mds"	involves: 129S2/SvPas * FVB	MP:0004215	abnormal myocardial fiber physiology	CCO:MP0004215
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm2.1Tyj>/Rbl2<tm2.1Tyj>,Tg(Pax6-cre,GFP)2Pgr/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0004179	transmission ratio distortion	CCO:MP0004179
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:105085	Rbl2	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:105085	Rbl2	"Kras<tm4Tyj>/Kras<+>,Rbl2<tm2Tyj>/Rbl2<tm2Tyj>"	involves: 129S4/SvJae	MP:0008014	lung tumor	CCO:MP0008014
MGI:105085	Rbl2	"Kras<tm4Tyj>/Kras<+>,Rbl2<tm2Tyj>/Rbl2<tm2Tyj>"	involves: 129S4/SvJae	MP:0002083	premature death	CCO:MP0002083
MGI:105085	Rbl2	"Kras<tm4Tyj>/Kras<+>,Rbl2<tm2Tyj>/Rbl2<tm2Tyj>"	involves: 129S4/SvJae	MP:0001179	thick alveolar septum	CCO:MP0001179
MGI:105085	Rbl2	"Kras<tm4Tyj>/Kras<+>,Rbl2<tm2Tyj>/Rbl2<tm2Tyj>"	involves: 129S4/SvJae	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:105085	Rbl2	"Kras<tm4Tyj>/Kras<+>,Rbl2<tm2Tyj>/Rbl2<tm2Tyj>"	involves: 129S4/SvJae	MP:0002267	abnormal bronchiole morphology	CCO:MP0002267
MGI:105085	Rbl2	"Kras<tm4Tyj>/Kras<+>,Rbl2<tm2Tyj>/Rbl2<tm2Tyj>"	involves: 129S4/SvJae	MP:0003721	increased tumor growth/size	CCO:MP0003721
MGI:105085	Rbl2	"Kras<tm4Tyj>/Kras<+>,Rbl2<tm2Tyj>/Rbl2<tm2Tyj>"	involves: 129S4/SvJae	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0008163	increased diameter of ulna	CCO:MP0008163
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000445	short snout	CCO:MP0000445
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0001270	distended abdomen	CCO:MP0001270
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0008218	delayed emergence of vibrissae	CCO:MP0008218
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002683	delayed fertility	CCO:MP0002683
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0008161	increased diameter of radius	CCO:MP0008161
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0008160	increased diameter of humerus	CCO:MP0008160
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004624	abnormal thoracic cage	CCO:MP0004624
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004359	short ulna	CCO:MP0004359
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004351	short humerus	CCO:MP0004351
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003704	abnormal hair follicle development	CCO:MP0003704
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<+>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0000932	absent notochord	CCO:MP0000932
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0003203	increased neuron apoptosis	CCO:MP0003203
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0002652	thin myocardial wall	CCO:MP0002652
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0000926	absent floor plate	CCO:MP0000926
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<+>"	involves: 129S2/SvPas * C57BL/6	MP:0000547	short limbs	CCO:MP0000547
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0000925	abnormal floor plate morphology	CCO:MP0000925
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003419	delayed endochondral bone ossification	CCO:MP0003419
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0000557	absent hindlimb	CCO:MP0000557
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0000274	enlarged heart	CCO:MP0000274
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0000737	abnormal myotome development	CCO:MP0000737
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0002084	abnormal developmental patterning	CCO:MP0002084
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0001689	incomplete somite formation	CCO:MP0001689
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000652	enlarged sebaceous gland	CCO:MP0000652
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0004355	short radius	CCO:MP0004355
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000402	abnormal zigzag hairs	CCO:MP0000402
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000397	abnormal guard hair	CCO:MP0000397
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000400	abnormal awl hair	CCO:MP0000400
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000379	decreased hair follicle number	CCO:MP0000379
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000383	abnormal hair follicle orientation	CCO:MP0000383
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003662	abnormal long bone epiphyseal plate proliferative zone	CCO:MP0003662
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000116	abnormal tooth development	CCO:MP0000116
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001239	abnormal epidermis stratum granulosum morphology	CCO:MP0001239
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002116	abnormal craniofacial bone morphology	CCO:MP0002116
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001270	distended abdomen	CCO:MP0001270
MGI:105085	Rbl2	Rbl2<tm1Tyj>/Rbl2<+>	involves: 129S2/SvPas * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:105085	Rbl2	Rbl2<tm1Tyj>/Rbl2<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000166	abnormal chondrocyte morphology	CCO:MP0000166
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000077	abnormal interparietal bone morphology	CCO:MP0000077
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003408	increased width of hypertrophic chondrocyte zone	CCO:MP0003408
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003120	abnormal tracheal cartilage morphology	CCO:MP0003120
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003055	abnormal long bone epiphyseal plate morphology	CCO:MP0003055
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0005358	abnormal incisor morphology	CCO:MP0005358
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002823	abnormal rib development	CCO:MP0002823
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0005296	abnormal humerus morphology	CCO:MP0005296
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000445	short snout	CCO:MP0000445
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000078	abnormal supraoccipital bone morphology	CCO:MP0000078
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000547	short limbs	CCO:MP0000547
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001957	apnea	CCO:MP0001957
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001951	abnormal breathing	CCO:MP0001951
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000382	underdeveloped hair follicles	CCO:MP0000382
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000125	absent incisors	CCO:MP0000125
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0001222	epidermal hyperplasia	CCO:MP0001222
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003427	parakeratosis	CCO:MP0003427
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002656	abnormal keratinocyte differentiation	CCO:MP0002656
MGI:105085	Rbl2	"Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Rbl2<tm1Tyj>/Rbl2<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000427	abnormal hair cycle	CCO:MP0000427
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0004180	failure of initiation of embryo turning	CCO:MP0004180
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:105085	Rbl2	Rbl2<tm1Mru>/Rbl2<tm1Mru>	involves: 129S4/SvJae * BALB/cJ	MP:0004251	failure of looping morphogenesis	CCO:MP0004251
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1929645	Rec8	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	MP:0001127	small ovary	CCO:MP0001127
MGI:1929645	Rec8	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1929645	Rec8	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1929645	Rec8	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0004805	absent oocytes	CCO:MP0004805
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0004196	abnormal prenatal growth/weight/body size	CCO:MP0004196
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0001925	male infertility	CCO:MP0001925
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1929645	Rec8	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	MP:0001924	infertility	CCO:MP0001924
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0001926	female infertility	CCO:MP0001926
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1929645	Rec8	Rec8<tm1Mjm>/Rec8<tm1Mjm>	either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6)	MP:0005159	azoospermia	CCO:MP0005159
MGI:1929645	Rec8	Rec8<mei8>/Rec8<mei8>	involves: 129S4/SvJae * C57BL/6J	MP:0001147	small testis	CCO:MP0001147
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000133	abnormal long bone metaphysis morphology	CCO:MP0000133
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000414	alopecia	CCO:MP0000414
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001212	skin lesions	CCO:MP0001212
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000128	growth retardation of molars	CCO:MP0000128
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000706	small thymus	CCO:MP0000706
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005171	absent coat pigmentation	CCO:MP0005171
MGI:1931028	Recql4	Recql4<tm1Furu>/Recql4<tm1Furu>	Not Specified	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1931028	Recql4	Recql4<tm1Furu>/Recql4<tm1Furu>	Not Specified	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005359	growth retardation of incisors	CCO:MP0005359
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008479	decreased spleen white pulp amount	CCO:MP0008479
MGI:1931028	Recql4	Recql4<tm1Abe>/Recql4<tm1Abe>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0009543	abnormal thymus corticomedullary boundary morphology	CCO:MP0009543
MGI:1931028	Recql4	Recql4<tm1Furu>/Recql4<tm1Furu>	Not Specified	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000111	cleft palate	CCO:MP0000111
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000413	polyphalangy	CCO:MP0000413
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000562	polydactyly	CCO:MP0000562
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:1931028	Recql4	"Apc<Min>/Apc<+>,Recql4<tm1Glu>/Recql4<tm1Glu>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:1931028	Recql4	"Apc<Min>/Apc<+>,Recql4<tm1Glu>/Recql4<tm1Glu>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002815	adenoma	CCO:MP0002815
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1931028	Recql4	"Apc<Min>/Apc<+>,Recql4<tm1Glu>/Recql4<tm1Glu>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005174	abnormal tail pigmentation	CCO:MP0005174
MGI:1931028	Recql4	Recql4<tm1Glu>/Recql4<tm1Glu>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1859709	Rgs14	Rgs14<tm1Lex>/Rgs14<tm1Lex>	involves: 129S5/SvEvBrd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1859709	Rgs14	Rgs14<tm1Pngr>/Rgs14<tm1Pngr>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0003406	failure of zygotic cell division	CCO:MP0003406
MGI:1859709	Rgs14	Rgs14<tm1Pngr>/Rgs14<tm1Pngr>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0008263	abnormal hippocampus CA1 region morphology	CCO:MP0008263
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0000249	abnormal blood vessel physiology	CCO:MP0000249
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0001363	increased anxiety-related response	CCO:MP0001363
MGI:1098271	Rgs2	Rgs2<tm1Dgen>/Rgs2<tm1Dgen>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0000530	abnormal kidney vasculature	CCO:MP0000530
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0001895	abnormal hippocampus function	CCO:MP0001895
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0005094	abnormal T cell proliferation	CCO:MP0005094
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<+>	involves: C57BL/6J	MP:0002842	increased blood pressure	CCO:MP0002842
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<+>	involves: C57BL/6J	MP:0000530	abnormal kidney vasculature	CCO:MP0000530
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0002842	increased blood pressure	CCO:MP0002842
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0002844	aortic hypertrophy	CCO:MP0002844
MGI:1098271	Rgs2	Rgs2<tm1Pngr>/Rgs2<tm1Pngr>	involves: C57BL/6J	MP:0005656	decreased aggression	CCO:MP0005656
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0008019	liver tumor	CCO:MP0008019
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0008000	ovary tumor	CCO:MP0008000
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0002947	hemangioma	CCO:MP0002947
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<tm1Whl>	Not Specified	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0005276	skin tumor	CCO:MP0005276
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<tm1Whl>	Not Specified	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0002014	papilloma	CCO:MP0002014
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0002022	lymphoma	CCO:MP0002022
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:1916233	Rint1	Rint1<tm1Whl>/Rint1<+>	Not Specified	MP:0002083	premature death	CCO:MP0002083
MGI:1101759	Rnf2	"Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * CBA	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:1101759	Rnf2	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1101759	Rnf2	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0000599	enlarged liver	CCO:MP0000599
MGI:1101759	Rnf2	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:1101759	Rnf2	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1101759	Rnf2	"Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * CBA	MP:0002144	abnormal B cell differentiation	CCO:MP0002144
MGI:1101759	Rnf2	"Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * CBA	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:1101759	Rnf2	"Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * CBA	MP:0000223	decreased monocyte cell number	CCO:MP0000223
MGI:1101759	Rnf2	"Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * CBA	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:1101759	Rnf2	"Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * CBA	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:1101759	Rnf2	"Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * CBA	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:1101759	Rnf2	"Polr2a<tm1(cre/ESR1)Bbd>/Polr2a<+>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * SJL	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:1101759	Rnf2	"Polr2a<tm1(cre/ESR1)Bbd>/Polr2a<+>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * SJL	MP:0005017	decreased B cell number	CCO:MP0005017
MGI:1101759	Rnf2	"Polr2a<tm1(cre/ESR1)Bbd>/Polr2a<+>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * SJL	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:1101759	Rnf2	"Cdkn2a<tm1Rdp>/Cdkn2a<tm1Rdp>,Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129 * C57BL/6J * C57BL/10 * CBA * SJL	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:1101759	Rnf2	"Rnf2<tm1Mvi>/Rnf2<tm1Mvi>,Tg(Mx1-cre)1Cgn/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10 * CBA	MP:0000333	decreased bone marrow cell number	CCO:MP0000333
MGI:1101759	Rnf2	Rnf2<tm1Mvl>/Rnf2<tm1Mvl>	either: (involves: 129/Ola) or (involves: 129/Ola * FVB)	MP:0001696	failure to gastrulate	CCO:MP0001696
MGI:1101759	Rnf2	Rnf2<tm1Mvl>/Rnf2<tm1Mvl>	either: (involves: 129/Ola) or (involves: 129/Ola * FVB)	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1101759	Rnf2	"Pcgf2<tm1Hko>/Pcgf2<tm1Hko>,Rnf2<tm1Hko>/Rnf2<tm1Hko>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000137	abnormal vertebrae morphology	CCO:MP0000137
MGI:1101759	Rnf2	"Pcgf2<tm1Hko>/Pcgf2<tm1Hko>,Rnf2<tm1Hko>/Rnf2<tm1Hko>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008146	asymmetric rib-sternum attachment	CCO:MP0008146
MGI:1101759	Rnf2	Rnf2<tm1Hko>/Rnf2<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004618	thoracic vertebral transformation	CCO:MP0004618
MGI:1101759	Rnf2	Rnf2<tm1Hko>/Rnf2<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0004615	cervical vertebral transformation	CCO:MP0004615
MGI:1101759	Rnf2	Rnf2<tm1Hko>/Rnf2<tm1Hko>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008277	abnormal sternum ossification	CCO:MP0008277
MGI:107926	Rock2	Rock2<tm1Sna>/Rock2<tm1Sna>	involves: 129X1/SvJ * C57BL/6	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:107926	Rock2	Rock2<tm1Sna>/Rock2<tm1Sna>	involves: 129X1/SvJ * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:107926	Rock2	Rock2<tm1Sna>/Rock2<tm1Sna>	involves: 129X1/SvJ * C57BL/6	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:107926	Rock2	Rock2<tm1Sna>/Rock2<tm1Sna>	involves: 129X1/SvJ * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:107926	Rock2	Rock2<tm1Sna>/Rock2<tm1Sna>	involves: 129X1/SvJ * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:107926	Rock2	Rock2<tm1Sna>/Rock2<tm1Sna>	involves: 129X1/SvJ * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1915525	Rpa1	Rpa1<tm1Wed>/Rpa1<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0005013	increased lymphocyte cell number	CCO:MP0005013
MGI:1915525	Rpa1	Rpa1<tm1Wed>/Rpa1<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0002022	lymphoma	CCO:MP0002022
MGI:1915525	Rpa1	Rpa1<tm1Wed>/Rpa1<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1915525	Rpa1	Rpa1<tm1Wed>/Rpa1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1915525	Rpa1	Rpa1<tm1Wed>/Rpa1<tm1Wed>	involves: 129/Sv * C57BL/6J * SJL	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1915525	Rpa1	Rpa1<tm1Wed>/Rpa1<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1915525	Rpa1	Rpa1<tm1Wed>/Rpa1<+>	involves: 129/Sv * C57BL/6J * SJL	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:1915443	Rpl24	"Tg(IghMyc)186Brn/0,Rpl24<Bst>/Rpl24<+>"	involves: C57BL/LiA * C57BLKS * CBA/BrA	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001330	abnormal optic nerve morphology	CCO:MP0001330
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0000373	belly spot	CCO:MP0000373
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0000562	polydactyly	CCO:MP0000562
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0000585	kinked tail	CCO:MP0000585
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0004619	caudal vertebral fusion	CCO:MP0004619
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0000592	short tail	CCO:MP0000592
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001304	cataracts	CCO:MP0001304
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001289	persistence of hyaloid capillary system	CCO:MP0001289
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0002984	retina hypoplasia	CCO:MP0002984
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0000914	exencephaly	CCO:MP0000914
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001539	decreased caudal vertebrae number	CCO:MP0001539
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0000120	malocclusion	CCO:MP0000120
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0002792	abnormal retinal vasculature	CCO:MP0002792
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001333	absent optic nerve	CCO:MP0001333
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0005262	coloboma	CCO:MP0005262
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0005241	abnormal retinal ganglion layer morphology	CCO:MP0005241
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0005098	abnormal choroid morphology	CCO:MP0005098
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0003099	retinal detachment	CCO:MP0003099
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0008516	disorganized retinal outer nuclear layer	CCO:MP0008516
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<Bst>	C57BLKS	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<Bst>	C57BLKS	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0002110	abnormal digit morphology	CCO:MP0002110
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0001265	decreased body size	CCO:MP0001265
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0004269	abnormal optic cup morphology	CCO:MP0004269
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0006071	abnormal retinal progenitor morphology	CCO:MP0006071
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0008512	disorganized retinal inner nuclear layer	CCO:MP0008512
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0008511	thin retinal inner nuclear layer	CCO:MP0008511
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0006214	asymmetrical orbits	CCO:MP0006214
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0006069	abnormal retinal neuronal layer morphology	CCO:MP0006069
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0003711	pathological neovascularization	CCO:MP0003711
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0008507	thin retinal ganglion layer	CCO:MP0008507
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0006243	impaired pupillary reflex	CCO:MP0006243
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0006221	optic nerve hypoplasia	CCO:MP0006221
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0003734	abnormal retinal inner plexiform layer morphology	CCO:MP0003734
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0004271	abnormal paw/hand/foot morphology	CCO:MP0004271
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0004650	increased lumbar vertebrae number	CCO:MP0004650
MGI:1915443	Rpl24	Rpl24<Bst>/Rpl24<+>	C57BLKS	MP:0004703	abnormal vertebral column	CCO:MP0004703
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0003059	decreased insulin secretion	CCO:MP0003059
MGI:98159	Rps6	"Rps6<tm1Gtho>/Rps6<tm1Gtho>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98159	Rps6	"Rps6<tm1Gtho>/Rps6<tm1Gtho>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005517	decreased liver regeneration	CCO:MP0005517
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0005293	impaired glucose tolerance	CCO:MP0005293
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002891	increased insulin sensitivity	CCO:MP0002891
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0005217	abnormal pancreatic beta cell morphology	CCO:MP0005217
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0002727	decreased circulating insulin level	CCO:MP0002727
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:98159	Rps6	Rps6<tm1Om>/Rps6<tm1Om>	involves: 129S1/Sv * 129X1/SvJ * ICR	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:98159	Rps6	"Rps6<tm1Gtho>/Rps6<tm1Gtho>,Tg(Mx1-cre)1Cgn/0"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0000358	abnormal cell content/ morphology	CCO:MP0000358
MGI:1194909	Rsph1	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	MP:0003698	abnormal male reproductive system physiology	CCO:MP0003698
MGI:1194909	Rsph1	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:1194909	Rsph1	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:1194909	Rsph1	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	MP:0004543	abnormal sperm physiology	CCO:MP0004543
MGI:1194909	Rsph1	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1194909	Rsph1	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:1194909	Rsph1	Rsph1<tm1Htan>/Rsph1<tm1Htan>	involves: 129S1/Sv * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6)	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:102672	Runx3	Runx3<tm2Yg>/Runx3<tm2Yg>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * ICR	MP:0005010	abnormal CD8-positive T cell morphology	CCO:MP0005010
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	involves: 129S1/Sv * 129X1/SvJ	MP:0004142	abnormal muscle tone	CCO:MP0004142
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	involves: 129S1/Sv * 129X1/SvJ	MP:0005010	abnormal CD8-positive T cell morphology	CCO:MP0005010
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	involves: 129S1/Sv * 129X1/SvJ	MP:0000162	lordosis	CCO:MP0000162
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	involves: 129S1/Sv * 129X1/SvJ	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	involves: 129S1/Sv * 129X1/SvJ	MP:0001393	ataxia	CCO:MP0001393
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	involves: 129S1/Sv * 129X1/SvJ	MP:0001504	abnormal posture	CCO:MP0001504
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	involves: 129S1/Sv * 129X1/SvJ	MP:0001265	decreased body size	CCO:MP0001265
MGI:102672	Runx3	Runx3<tm2Yg>/Runx3<tm2Yg>	involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * ICR	MP:0008115	abnormal dendritic cell differentiation	CCO:MP0008115
MGI:102672	Runx3	"Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008080	abnormal CD8-positive T cell differentiation	CCO:MP0008080
MGI:102672	Runx3	"Runx1<tm1Toku>/Runx1<+>,Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:102672	Runx3	"Runx1<tm1Toku>/Runx1<tm1Toku>,Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:102672	Runx3	"Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0002495	increased IgA level	CCO:MP0002495
MGI:102672	Runx3	"Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0005010	abnormal CD8-positive T cell morphology	CCO:MP0005010
MGI:102672	Runx3	"H2-Ab1<tm1Gru>/H2-Ab1<tm1Gru>,Runx1<tm1Toku>/Runx1<tm1Toku>,Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * DBA/2	MP:0008555	abnormal interferon secretion	CCO:MP0008555
MGI:102672	Runx3	"Runx1<tm1Toku>/Runx1<tm1Toku>,Runx3<tm1Itan>/Runx3<+>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:102672	Runx3	"H2-Ab1<tm1Gru>/H2-Ab1<tm1Gru>,Runx1<tm1Toku>/Runx1<tm1Toku>,Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * DBA/2	MP:0008074	increased CD4-positive T cell number	CCO:MP0008074
MGI:102672	Runx3	"Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0001861	lung inflammation	CCO:MP0001861
MGI:102672	Runx3	"Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:102672	Runx3	"Runx1<tm1Toku>/Runx1<tm1Toku>,Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:102672	Runx3	"Runx1<tm1Tani>/Runx1<tm1Tani>,Runx3<tm1Itan>/Runx3<tm1Itan>,Tg(CD4-cre)1Cwi/?"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:102672	Runx3	Runx3<tm1Litt>/Runx3<tm1Litt>	involves: 129P2/OlaHsd	MP:0008080	abnormal CD8-positive T cell differentiation	CCO:MP0008080
MGI:102672	Runx3	Runx3<tm1Litt>/Runx3<tm1Litt>	involves: 129P2/OlaHsd	MP:0002408	abnormal double-positive T cell morphology	CCO:MP0002408
MGI:102672	Runx3	"Runx1<tm1Toku>/Runx1<tm1Toku>,Runx3<tm1Itan>/Runx3<+>,Tg(CD4-cre)1Cwi/0"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2	MP:0008075	decreased CD4-positive T cell number	CCO:MP0008075
MGI:102672	Runx3	Runx3<tm1Yito>/Runx3<tm1Yito>	involves: 129P2/OlaHsd * C57BL/6	MP:0000716	abnormal immune system cell morphology	CCO:MP0000716
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000416	sparse hair	CCO:MP0000416
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000402	abnormal zigzag hairs	CCO:MP0000402
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000405	abnormal auchene hairs	CCO:MP0000405
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000162	lordosis	CCO:MP0000162
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001393	ataxia	CCO:MP0001393
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001504	abnormal posture	CCO:MP0001504
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0002133	abnormal respiratory system physiology	CCO:MP0002133
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001845	abnormal inflammatory response	CCO:MP0001845
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001265	decreased body size	CCO:MP0001265
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000489	abnormal large intestine morphology	CCO:MP0000489
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0005209	abnormal gastric mucosa morphology	CCO:MP0005209
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000490	abnormal crypts of Lieberkuhn morphology	CCO:MP0000490
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001663	abnormal digestive system physiology	CCO:MP0001663
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0008118	absent Langerhans cell	CCO:MP0008118
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000964	small dorsal root ganglion	CCO:MP0000964
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0003994	abnormal dorsal spinal root morphology	CCO:MP0003994
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0004142	abnormal muscle tone	CCO:MP0004142
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0004140	abnormal chief cell morphology	CCO:MP0004140
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0004139	abnormal gastric parietal cell morphology	CCO:MP0004139
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0006282	abnormal spinal cord dorsal horn morphology	CCO:MP0006282
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0003306	small intestinal inflammation	CCO:MP0003306
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0008115	abnormal dendritic cell differentiation	CCO:MP0008115
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0002912	abnormal excitatory postsynaptic potential	CCO:MP0002912
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0008126	increased dendritic cell number	CCO:MP0008126
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0008468	absent muscle spindles	CCO:MP0008468
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0008713	abnormal cytokine level	CCO:MP0008713
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0008750	abnormal interferon level	CCO:MP0008750
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0008751	abnormal interleukin level	CCO:MP0008751
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0008752	abnormal tumor necrosis factor level	CCO:MP0008752
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0009677	abnormal spinal cord dorsal column morphology	CCO:MP0009677
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0006382	abnormal lung epithelium morphology	CCO:MP0006382
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0002376	abnormal dendritic cell physiology	CCO:MP0002376
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001873	stomach inflammation	CCO:MP0001873
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0002272	abnormal nervous system electrophysiology	CCO:MP0002272
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000494	abnormal cecum morphology	CCO:MP0000494
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000495	abnormal colon morphology	CCO:MP0000495
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000956	decreased spinal cord size	CCO:MP0000956
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001861	lung inflammation	CCO:MP0001861
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0003910	decreased eating behavior	CCO:MP0003910
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0002497	increased IgE level	CCO:MP0002497
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001858	intestinal inflammation	CCO:MP0001858
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000967	abnormal sensory neuron projections	CCO:MP0000967
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0001952	increased airway responsiveness	CCO:MP0001952
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0005232	abnormal mesenteric lymph node morphology	CCO:MP0005232
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0002816	colitis	CCO:MP0002816
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0005454	decreased adipose tissue amount	CCO:MP0005454
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0005461	abnormal dendritic cell morphology	CCO:MP0005461
MGI:102672	Runx3	Runx3<tm1Yg>/Runx3<tm1Yg>	either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1)	MP:0000965	abnormal sensory neuron morphology	CCO:MP0000965
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<+>	involves: 129P2/OlaHsd	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<+>	involves: 129P2/OlaHsd	MP:0002423	abnormal mast cell physiology	CCO:MP0002423
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<+>	involves: 129P2/OlaHsd	MP:0003135	increased erythroid progenitor cell number	CCO:MP0003135
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<+>	involves: 129P2/OlaHsd	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<tm1Hnaka>	involves: 129P2/OlaHsd	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<tm1Hnaka>	involves: 129P2/OlaHsd	MP:0002423	abnormal mast cell physiology	CCO:MP0002423
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<tm1Hnaka>	involves: 129P2/OlaHsd	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<tm1Hnaka>	involves: 129P2/OlaHsd	MP:0002459	abnormal B cell physiology	CCO:MP0002459
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<tm1Hnaka>	involves: 129P2/OlaHsd	MP:0003135	increased erythroid progenitor cell number	CCO:MP0003135
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<tm1Hnaka>	involves: 129P2/OlaHsd	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<tm1Hnaka>	involves: 129P2/OlaHsd	MP:0006410	abnormal common myeloid progenitor cell morphology	CCO:MP0006410
MGI:1913656	Sac3d1	Sac3d1<tm1Hnaka>/Sac3d1<tm1Hnaka>	involves: 129P2/OlaHsd	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:1345148	Sept3	Sept3<Gt(2-86)Stmn>/Sept3<Gt(2-86)Stmn>	involves: 129/Sv	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1270156	Sept4	Sept4<tm1Hs>/Sept4<tm1Hs>	involves: 129/Sv * C57BL/6J	MP:0003666	impaired sperm capacitation	CCO:MP0003666
MGI:1270156	Sept4	Sept4<tm1Ksh>/Sept4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	MP:0005578	teratozoospermia	CCO:MP0005578
MGI:1270156	Sept4	Sept4<tm1Hs>/Sept4<+>	involves: 129/Sv * C57BL/6J	MP:0005578	teratozoospermia	CCO:MP0005578
MGI:1270156	Sept4	Sept4<tm1Hs>/Sept4<tm1Hs>	involves: 129/Sv * C57BL/6J	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:1270156	Sept4	Sept4<tm1Hs>/Sept4<tm1Hs>	involves: 129/Sv * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:1270156	Sept4	Sept4<tm1Ksh>/Sept4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:1270156	Sept4	Sept4<tm1Ksh>/Sept4<tm1Ksh>	involves: 129X1/SvJ * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:1270156	Sept4	Sept4<tm1Hs>/Sept4<tm1Hs>	involves: 129/Sv * C57BL/6J	MP:0005578	teratozoospermia	CCO:MP0005578
MGI:1195461	Sept5	Sept5<tm1Wtr>/Sept5<tm1Wtr>	involves: 129S1/Sv * 129X1/SvJ	MP:0005464	abnormal platelet physiology	CCO:MP0005464
MGI:1195461	Sept5	Sept5<tm1Wtr>/Sept5<tm1Wtr>	involves: 129S1/Sv * 129X1/SvJ	MP:0009586	increased platelet aggregation	CCO:MP0009586
MGI:1195461	Sept5	Sept5<tm1Wtr>/Sept5<tm1Wtr>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0002557	abnormal social/conspecific interaction	CCO:MP0002557
MGI:1195461	Sept5	Sept5<tm1Wtr>/Sept5<tm1Wtr>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001364	decreased anxiety-related response	CCO:MP0001364
MGI:1195461	Sept5	Sept5<tm1Wtr>/Sept5<tm1Wtr>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0009141	increased prepulse inhibition	CCO:MP0009141
MGI:1195461	Sept5	Sept5<tm1Wtr>/Sept5<tm1Wtr>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001488	increased startle reflex	CCO:MP0001488
MGI:1195461	Sept5	Sept5<tm1Wtr>/Sept5<tm1Wtr>	involves: 129S1/Sv * 129X1/SvJ * CD-1	MP:0001463	abnormal spatial learning	CCO:MP0001463
MGI:1888939	Sept6	Sept6<tm1Nosa>/Sept6<tm1Nosa>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1888939	Sept6	Sept6<tm1Nosa>/Y	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1915206	Setd8	Setd8<Gt(RRB075)Byg>/Setd8<Gt(RRB075)Byg>	involves: 129P2/OlaHsd	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1095403	Sf1	Sf1<Gt(pU17)1Teya>/Sf1<Gt(pU17)1Teya>	involves: C57BL/6 * CBA	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:1095403	Sf1	Sf1<Gt(pU17)1Teya>/Sf1<+>	involves: C57BL/6 * CBA	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:1095403	Sf1	Sf1<Gt(pU17)1Teya>/Sf1<+>	involves: C57BL/6 * CBA	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:1891831	Sfn	Sfn<Er>/Sfn<+>	involves: 129S/SvEv * C57BL/6By	MP:0002051	skin papilloma	CCO:MP0002051
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0009474	thick epidermis stratum spinosum	CCO:MP0009474
MGI:1891831	Sfn	Sfn<Er>/Sfn<+>	involves: 129S/SvEv * C57BL/6By	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000111	cleft palate	CCO:MP0000111
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000452	abnormal mouth morphology	CCO:MP0000452
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000564	syndactyly	CCO:MP0000564
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0000585	kinked tail	CCO:MP0000585
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001219	thickened epidermis	CCO:MP0001219
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001233	abnormal epidermis suprabasal layer morphology	CCO:MP0001233
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001241	absent epidermis stratum corneum	CCO:MP0001241
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003937	abnormal limbs/digits/tail development	CCO:MP0003937
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0009560	absent epidermis stratum granulosum	CCO:MP0009560
MGI:1891831	Sfn	"Irf6<tm1Mjd>/Irf6<+>,Sfn<Er>/Sfn<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0003160	abnormal esophageal development	CCO:MP0003160
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0001219	thickened epidermis	CCO:MP0001219
MGI:1891831	Sfn	Sfn<Er>/Sfn<+>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0005114	premature hair loss	CCO:MP0005114
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0009560	absent epidermis stratum granulosum	CCO:MP0009560
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0003935	abnormal craniofacial development	CCO:MP0003935
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0002656	abnormal keratinocyte differentiation	CCO:MP0002656
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0001954	respiratory distress	CCO:MP0001954
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0001196	shiny skin	CCO:MP0001196
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0001222	epidermal hyperplasia	CCO:MP0001222
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0000592	short tail	CCO:MP0000592
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0000547	short limbs	CCO:MP0000547
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	B6CBACa A<w-J>/A-Sfn<Er>/J	MP:0001241	absent epidermis stratum corneum	CCO:MP0001241
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0006033	abnormal external auditory canal	CCO:MP0006033
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0002111	abnormal tail morphology	CCO:MP0002111
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0009553	fused lips	CCO:MP0009553
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0000454	abnormal jaw morphology	CCO:MP0000454
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0004537	abnormal palatine shelf	CCO:MP0004537
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0004174	abnormal spine curvature	CCO:MP0004174
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0000433	microcephaly	CCO:MP0000433
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0002234	abnormal pharynx morphology	CCO:MP0002234
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0000447	flattened snout	CCO:MP0000447
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0000018	small ears	CCO:MP0000018
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0001297	microphthalmia	CCO:MP0001297
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0002251	abnormal nasopharynx morphology	CCO:MP0002251
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0002237	abnormal nasal cavity morphology	CCO:MP0002237
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0001340	abnormal eyelid morphology	CCO:MP0001340
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0002235	abnormal external nares morphology	CCO:MP0002235
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0000762	abnormal tongue morphology	CCO:MP0000762
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0003743	abnormal facial morphology	CCO:MP0003743
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0003769	abnormal lip morphology	CCO:MP0003769
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0000432	abnormal head morphology	CCO:MP0000432
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	Not Specified	MP:0000458	abnormal mandible morphology	CCO:MP0000458
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0009263	abnormal eyelid fusion	CCO:MP0009263
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0004576	abnormal foot plate morphology	CCO:MP0004576
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0004575	small limb buds	CCO:MP0004575
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0003935	abnormal craniofacial development	CCO:MP0003935
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0003671	abnormal eyelid aperture	CCO:MP0003671
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0005650	abnormal limb bud morphology	CCO:MP0005650
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0001676	abnormal apical ectodermal ridge	CCO:MP0001676
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0001297	microphthalmia	CCO:MP0001297
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0001218	thin epidermis	CCO:MP0001218
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0001219	thickened epidermis	CCO:MP0001219
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0001236	abnormal epidermis stratum spinosum morphology	CCO:MP0001236
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0000592	short tail	CCO:MP0000592
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0000585	kinked tail	CCO:MP0000585
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0003937	abnormal limbs/digits/tail development	CCO:MP0003937
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0000564	syndactyly	CCO:MP0000564
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0001231	abnormal epidermis stratum basale morphology	CCO:MP0001231
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	involves: C57BL/6By	MP:0000384	distorted hair follicle pattern	CCO:MP0000384
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001239	abnormal epidermis stratum granulosum morphology	CCO:MP0001239
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001240	abnormal epidermis stratum corneum morphology	CCO:MP0001240
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001231	abnormal epidermis stratum basale morphology	CCO:MP0001231
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0002235	abnormal external nares morphology	CCO:MP0002235
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000547	short limbs	CCO:MP0000547
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001196	shiny skin	CCO:MP0001196
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000379	decreased hair follicle number	CCO:MP0000379
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000018	small ears	CCO:MP0000018
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000160	kyphosis	CCO:MP0000160
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0002543	brachyphalangia	CCO:MP0002543
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000552	abnormal radius morphology	CCO:MP0000552
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001953	respiratory failure	CCO:MP0001953
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0002233	abnormal nose morphology	CCO:MP0002233
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000445	short snout	CCO:MP0000445
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:1891831	Sfn	Sfn<Er>/Sfn<+>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0008569	lethality at weaning	CCO:MP0008569
MGI:1891831	Sfn	Sfn<Er>/Sfn<+>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0005114	premature hair loss	CCO:MP0005114
MGI:1891831	Sfn	Sfn<Er>/Sfn<+>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1891831	Sfn	Sfn<Er>/Sfn<+>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000416	sparse hair	CCO:MP0000416
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0003775	thin lip	CCO:MP0003775
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0003315	abnormal perineum morphology	CCO:MP0003315
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001199	thin skin	CCO:MP0001199
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001954	respiratory distress	CCO:MP0001954
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001539	decreased caudal vertebrae number	CCO:MP0001539
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0005155	herniated intestine	CCO:MP0005155
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0002315	abnormal respiratory signs/symptoms	CCO:MP0002315
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0001297	microphthalmia	CCO:MP0001297
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0003744	abnormal orofacial morphology	CCO:MP0003744
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000452	abnormal mouth morphology	CCO:MP0000452
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000111	cleft palate	CCO:MP0000111
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:1891831	Sfn	Sfn<Er>/Sfn<Er>	either: (involves: 129/Sv * C57BL/6) or (involves: C57BL/6)	MP:0003130	anal atresia	CCO:MP0003130
MGI:1098767	Sgol2	Sgol2<Gt(D025B05)Wrst>/Sgol2<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1098767	Sgol2	Sgol2<Gt(D025B05)Wrst>/Sgol2<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1098767	Sgol2	Sgol2<Gt(D025B05)Wrst>/Sgol2<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:1098767	Sgol2	Sgol2<Gt(D025B05)Wrst>/Sgol2<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1098767	Sgol2	Sgol2<Gt(D025B05)Wrst>/Sgol2<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1098767	Sgol2	Sgol2<Gt(D025B05)Wrst>/Sgol2<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:1098767	Sgol2	Sgol2<Gt(D025B05)Wrst>/Sgol2<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:1098767	Sgol2	Sgol2<Gt(D025B05)Wrst>/Sgol2<Gt(D025B05)Wrst>	involves: 129S2/SvPas * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0006304	abnormal seminiferous epithelium morphology	CCO:MP0006304
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0005159	azoospermia	CCO:MP0005159
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0001147	small testis	CCO:MP0001147
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0001262	decreased body weight	CCO:MP0001262
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0000601	small liver	CCO:MP0000601
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:108064	Siah1a	"Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>,Siah2<tm1Ddlb>/Siah2<+>"	involves: 129S4/SvJae * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:108064	Siah1a	"Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>,Siah2<tm1Ddlb>/Siah2<tm1Ddlb>"	involves: 129S4/SvJae * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:108064	Siah1a	Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>	involves: 129S1/Sv * C57BL/6J	MP:0001919	abnormal reproductive system physiology	CCO:MP0001919
MGI:108064	Siah1a	"Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>,Siah2<tm1Ddlb>/Siah2<tm1Ddlb>"	involves: 129S4/SvJae * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:108062	Siah2	"Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>,Siah2<tm1Ddlb>/Siah2<+>"	involves: 129S4/SvJae * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:108062	Siah2	"Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>,Siah2<tm1Ddlb>/Siah2<tm1Ddlb>"	involves: 129S4/SvJae * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:108062	Siah2	Siah2<tm1Ddlb>/Siah2<tm1Ddlb>	involves: 129S4/SvJae * C57BL/6J	MP:0002397	abnormal bone marrow morphology	CCO:MP0002397
MGI:108062	Siah2	"Siah1a<tm1Ddlb>/Siah1a<tm1Ddlb>,Siah2<tm1Ddlb>/Siah2<tm1Ddlb>"	involves: 129S4/SvJae * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:107157	Sin3a	Sin3a<tm1Rdp>/Sin3a<tm1Rdp>	involves: 129 * C57BL/6 * SJL	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:107157	Sin3a	Sin3a<tm1.1Rdp>/Sin3a<tm1.1Rdp>	involves: 129	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0005481	chronic myelocytic leukemia	CCO:MP0005481
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0005481	chronic myelocytic leukemia	CCO:MP0005481
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0002875	decreased erythrocyte cell number	CCO:MP0002875
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0004809	increased hematopoietic stem cell number	CCO:MP0004809
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0005152	pancytopenia	CCO:MP0005152
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<+>	involves: 129P2/OlaHsd * C57BL/6	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0000693	spleen hyperplasia	CCO:MP0000693
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0000321	increased bone marrow cell number	CCO:MP0000321
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0000218	increased leukocyte cell number	CCO:MP0000218
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0000322	increased granulocyte number	CCO:MP0000322
MGI:107576	Sipa1	Sipa1<tm1Nm>/Sipa1<tm1Nm>	involves: 129P2/OlaHsd * C57BL/6	MP:0000240	extramedullary hematopoiesis	CCO:MP0000240
MGI:1351663	Skp2	Skp2<tm1Kin>/Skp2<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:1351663	Skp2	Skp2<tm1Kin>/Skp2<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:1351663	Skp2	Skp2<tm1Kin>/Skp2<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:1351663	Skp2	Skp2<tm1Kin>/Skp2<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:1351663	Skp2	Skp2<tm1Kin>/Skp2<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:1351663	Skp2	Skp2<tm1Kin>/Skp2<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:1351663	Skp2	Skp2<tm1Kin>/Skp2<tm1Kin>	involves: 129P2/OlaHsd * C57BL/6	MP:0002908	delayed wound healing	CCO:MP0002908
MGI:2385046	Slc26a8	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	MP:0004542	impaired acrosome reaction	CCO:MP0004542
MGI:2385046	Slc26a8	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:2385046	Slc26a8	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:2385046	Slc26a8	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	MP:0001925	male infertility	CCO:MP0001925
MGI:2385046	Slc26a8	Slc26a8<tm1Ggac>/Slc26a8<tm1Ggac>	involves: 129S/SvEvBrd	MP:0006362	abnormal male germ cell morphology	CCO:MP0006362
MGI:1313259	Slfn1	Slfn1<tm1Hed>/Slfn1<tm1Hed>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1328366	Smarcb1	"Smarcb1<tm1Mya>/Smarcb1<tm2Mya>,Tg(Alb1-cre)7Gsc/0"	involves: 129S2/SvPas * FVB/N	MP:0002715	decreased glycogen catabolism rate	CCO:MP0002715
MGI:1328366	Smarcb1	"Smarcb1<tm1Mya>/Smarcb1<tm2Mya>,Tg(Alb1-cre)7Gsc/0"	involves: 129S2/SvPas * FVB/N	MP:0005439	decreased glycogen level	CCO:MP0005439
MGI:1328366	Smarcb1	"Smarcb1<tm1Mya>/Smarcb1<tm2Mya>,Tg(Alb1-cre)7Gsc/0"	involves: 129S2/SvPas * FVB/N	MP:0003383	abnormal gluconeogenesis	CCO:MP0003383
MGI:1328366	Smarcb1	"Smarcb1<tm1Mya>/Smarcb1<tm2Mya>,Tg(Alb1-cre)7Gsc/0"	involves: 129S2/SvPas * FVB/N	MP:0003893	increased hepatocyte proliferation	CCO:MP0003893
MGI:1328366	Smarcb1	"Smarcb1<tm1Mya>/Smarcb1<tm2Mya>,Tg(Alb1-cre)7Gsc/0"	involves: 129S2/SvPas * FVB/N	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1328366	Smarcb1	"Smarcb1<tm1Mya>/Smarcb1<tm2Mya>,Tg(Alb1-cre)7Gsc/0"	involves: 129S2/SvPas * FVB/N	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:1328366	Smarcb1	"Smarcb1<tm1Mya>/Smarcb1<tm2Mya>,Tg(Alb1-cre)7Gsc/0"	involves: 129S2/SvPas * FVB/N	MP:0000608	dissociated hepatocytes	CCO:MP0000608
MGI:1328366	Smarcb1	"Smarcb1<tm1Mya>/Smarcb1<tm2Mya>,Tg(Alb1-cre)7Gsc/0"	involves: 129S2/SvPas * FVB/N	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0002429	abnormal blood cell morphology/development	CCO:MP0002429
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0006139	rhabdomyoma	CCO:MP0006139
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm2Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Gata1-cre)1Sho/?"	involves: 129S1/Sv * 129S6/SvEvTac * CD1	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm2Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0000465	gastrointestinal hemorrhage	CCO:MP0000465
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0005011	increased eosinophil cell number	CCO:MP0005011
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm2Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm2Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0005152	pancytopenia	CCO:MP0005152
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0000689	abnormal spleen morphology	CCO:MP0000689
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0002339	abnormal lymph node morphology	CCO:MP0002339
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0000599	enlarged liver	CCO:MP0000599
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm2Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0009275	bruising	CCO:MP0009275
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0002022	lymphoma	CCO:MP0002022
MGI:1328366	Smarcb1	"Smarcb1<tm1Sho>/Smarcb1<tm3Sho>,Tg(Mx1-cre)1Cgn/?"	involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:1328366	Smarcb1	Smarcb1<Gt(OST32815)Lex>/Smarcb1<Gt(OST32815)Lex>	either: (involves: 129 * 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)	MP:0005028	abnormal trophectoderm morphology	CCO:MP0005028
MGI:1328366	Smarcb1	Smarcb1<Gt(OST32815)Lex>/Smarcb1<+>	either: (involves: 129 * 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1328366	Smarcb1	Smarcb1<Gt(OST32815)Lex>/Smarcb1<Gt(OST32815)Lex>	either: (involves: 129 * 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)	MP:0001728	failure of embryo implantation	CCO:MP0001728
MGI:1328366	Smarcb1	Smarcb1<Gt(OST32815)Lex>/Smarcb1<Gt(OST32815)Lex>	either: (involves: 129 * 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:1328366	Smarcb1	Smarcb1<Gt(OST32815)Lex>/Smarcb1<Gt(OST32815)Lex>	either: (involves: 129 * 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1328366	Smarcb1	Smarcb1<Gt(OST32815)Lex>/Smarcb1<Gt(OST32815)Lex>	either: (involves: 129 * 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6)	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:1328366	Smarcb1	Smarcb1<tm1Mya>/Smarcb1<+>	involves: 129S2/SvPas * C57BL/6	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:1328366	Smarcb1	Smarcb1<tm1Mya>/Smarcb1<tm1Mya>	involves: 129S2/SvPas * C57BL/6	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:1328366	Smarcb1	Smarcb1<tm1Mya>/Smarcb1<tm1Mya>	involves: 129S2/SvPas * C57BL/6	MP:0005028	abnormal trophectoderm morphology	CCO:MP0005028
MGI:1328366	Smarcb1	Smarcb1<tm1Mya>/Smarcb1<tm1Mya>	involves: 129S2/SvPas * C57BL/6	MP:0001728	failure of embryo implantation	CCO:MP0001728
MGI:1328366	Smarcb1	Smarcb1<tm1Sho>/Smarcb1<+>	involves: 129S6/SvEvTac * C57BL/6	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:1328366	Smarcb1	Smarcb1<tm1Sho>/Smarcb1<+>	involves: 129S6/SvEvTac * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1328366	Smarcb1	Smarcb1<tm1Gvk>/Smarcb1<tm1Gvk>	involves: 129/Sv * C57BL/6J * SJL/J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1328366	Smarcb1	Smarcb1<tm1Mya>/Smarcb1<tm1Mya>	involves: 129S2/SvPas * C57BL/6	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1328366	Smarcb1	Smarcb1<tm1Sho>/Smarcb1<tm1Sho>	involves: 129S6/SvEvTac * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1328366	Smarcb1	Smarcb1<tm1Mya>/Smarcb1<+>	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1328366	Smarcb1	Smarcb1<tm1Mya>/Smarcb1<tm1Mya>	involves: 129S2/SvPas * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1328366	Smarcb1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Smarcb1<tm1Gvk>/Smarcb1<+>"	involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J	MP:0001286	abnormal eye development	CCO:MP0001286
MGI:1328366	Smarcb1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Smarcb1<tm1Gvk>/Smarcb1<+>"	involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:1328366	Smarcb1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Smarcb1<tm1Gvk>/Smarcb1<+>"	involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J	MP:0003861	abnormal nervous system development	CCO:MP0003861
MGI:1328366	Smarcb1	Smarcb1<tm1Gvk>/Smarcb1<+>	involves: 129/Sv * C57BL/6J * SJL/J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1328366	Smarcb1	Smarcb1<tm1Gvk>/Smarcb1<+>	involves: 129/Sv * C57BL/6J * SJL/J	MP:0008018	facial tumor	CCO:MP0008018
MGI:1328366	Smarcb1	Smarcb1<tm1Gvk>/Smarcb1<+>	involves: 129/Sv * C57BL/6J * SJL/J	MP:0008021	blastoma	CCO:MP0008021
MGI:1328366	Smarcb1	"Ccnd1<tm1Wbg>/Ccnd1<tm1Wbg>,Smarcb1<tm1Gvk>/Smarcb1<+>"	involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J	MP:0001265	decreased body size	CCO:MP0001265
MGI:1344345	Smc1a	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	MP:0008404	increased cellular sensitivity to methylmethanesulfonate	CCO:MP0008404
MGI:1344345	Smc1a	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0005432	abnormal pro-B cell morphology	CCO:MP0005432
MGI:1344345	Smc1a	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:1344345	Smc1a	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0005089	decreased double-negative T cell number	CCO:MP0005089
MGI:1344345	Smc1a	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0001577	anemia	CCO:MP0001577
MGI:1344345	Smc1a	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0002396	abnormal hematopoietic system morphology/development	CCO:MP0002396
MGI:1344345	Smc1a	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:1344345	Smc1a	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:1344345	Smc1a	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:1344345	Smc1a	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Smc1a<tm1Mbk>/Smc1a<tm1Mbk>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0003884	decreased macrophage cell number	CCO:MP0003884
MGI:1344345	Smc1a	Smc1a<tm1Mbk>/Y	involves: 129S1/Sv * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:2154049	Smc1b	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	MP:0001924	infertility	CCO:MP0001924
MGI:2154049	Smc1b	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:2154049	Smc1b	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:2154049	Smc1b	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:2154049	Smc1b	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:2154049	Smc1b	Smc1b<tm1Jess>/Smc1b<tm1Jess>	involves: 129S6/SvEvTac * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0005473	decreased triiodothyronine level	CCO:MP0005473
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0001739	abnormal adrenal gland secretion	CCO:MP0001739
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0001255	decreased body height	CCO:MP0001255
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0000633	abnormal pituitary gland morphology	CCO:MP0000633
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0002427	disproportionate dwarf	CCO:MP0002427
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0000559	abnormal femur morphology	CCO:MP0000559
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0002187	abnormal fibula morphology	CCO:MP0002187
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0000558	abnormal tibia morphology	CCO:MP0000558
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0003723	abnormal long bone morphology	CCO:MP0003723
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0001131	abnormal ovarian follicle morphology	CCO:MP0001131
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0008341	decreased corticotroph cell number	CCO:MP0008341
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0001938	delayed sexual maturation	CCO:MP0001938
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0005471	decreased thyroxine level	CCO:MP0005471
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0003409	decreased width of hypertrophic chondrocyte zone	CCO:MP0003409
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0004163	abnormal adenohypophysis morphology	CCO:MP0004163
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0004201	fetal growth retardation	CCO:MP0004201
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0004701	decreased circulating insulin-like growth factor I level	CCO:MP0004701
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0008329	decreased somatotroph cell number	CCO:MP0008329
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0008335	decreased gonadotroph cell number	CCO:MP0008335
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0008338	decreased thyrotroph cell number	CCO:MP0008338
MGI:1927578	Smpd3	Smpd3<tm1Wst>/Smpd3<tm1Wst>	involves: 129S1/Sv	MP:0000060	delayed bone ossification	CCO:MP0000060
MGI:1927470	Spag5	Spag5<tm1Vdh>/Spag5<tm1Vdh>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1858896	Spast	Spast<tm1.1Jme>/Spast<tm1.1Jme>	involves: C57BL/6J	MP:0001407	short stride length	CCO:MP0001407
MGI:1858896	Spast	Spast<tm1.1Jme>/Spast<+>	involves: C57BL/6J	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:1858896	Spast	Spast<tm1.1Jme>/Spast<tm1.1Jme>	involves: C57BL/6J	MP:0001924	infertility	CCO:MP0001924
MGI:1858896	Spast	Spast<tm1Jme>/Spast<tm1Jme>	involves: C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1858896	Spast	Spast<tm1.1Jme>/Spast<tm1.1Jme>	involves: C57BL/6J	MP:0001406	abnormal gait	CCO:MP0001406
MGI:1858896	Spast	Spast<tm1.1Jme>/Spast<tm1.1Jme>	involves: C57BL/6J	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:1858896	Spast	Spast<m1Gri>/Spast<m1Gri>	B6.C-Spast<m1Gri>	MP:0001406	abnormal gait	CCO:MP0001406
MGI:1858896	Spast	Spast<m1Gri>/Spast<m1Gri>	B6.C-Spast<m1Gri>	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:1858896	Spast	Spast<m1Gri>/Spast<m1Gri>	B6.C-Spast<m1Gri>	MP:0004768	abnormal axonal transport	CCO:MP0004768
MGI:1858896	Spast	Spast<m1Gri>/Spast<+>	B6.C-Spast<m1Gri>	MP:0005404	abnormal axon morphology	CCO:MP0005404
MGI:1858896	Spast	Spast<m1Gri>/Spast<+>	B6.C-Spast<m1Gri>	MP:0004768	abnormal axonal transport	CCO:MP0004768
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129 * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1349669	Spo11	"Mael<tm1Bort>/Mael<tm1Bort>,Spo11<tm1Rdco>/Spo11<tm1Rdco>"	involves: 129 * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0002160	abnormal reproductive system morphology	CCO:MP0002160
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001925	male infertility	CCO:MP0001925
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001926	female infertility	CCO:MP0001926
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001147	small testis	CCO:MP0001147
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0002216	abnormal seminiferous tubule morphology	CCO:MP0002216
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:1349669	Spo11	Spo11<tm1Rdco>/Spo11<tm1Rdco>	involves: 129S6/SvEvTac	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac * C57BL/6	MP:0002225	abnormal spleen cellularity	CCO:MP0002225
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	C.129S6-Stat5a<tm1Mam>	MP:0005462	abnormal mast cell differentiation	CCO:MP0005462
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	C.129S6-Stat5a<tm1Mam>	MP:0000336	decreased mast cell number	CCO:MP0000336
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	C.129S6-Stat5a<tm1Mam>	MP:0000359	abnormal mast cell morphology	CCO:MP0000359
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac * C57BL/6	MP:0005070	impaired NK cell cytolysis	CCO:MP0005070
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac * C57BL/6	MP:0008045	decreased NK cell number	CCO:MP0008045
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac	MP:0001168	abnormal prostate epithelium morphology	CCO:MP0001168
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac	MP:0001158	abnormal prostate morphology	CCO:MP0001158
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0006269	abnormal mammary gland growth during pregnancy	CCO:MP0006269
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0006270	abnormal mammary gland growth during lactation	CCO:MP0006270
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	either: 129S6/SvEvTac-Stat5a<tm1Mam> or (involves: 129S6/SvEvTac * NIH Black Swiss)	MP:0001882	abnormal lactation	CCO:MP0001882
MGI:103036	Stat5a	Stat5a<tm1Mam>/Stat5a<tm1Mam>	involves: 129S6/SvEvTac	MP:0003607	abnormal prostate physiology	CCO:MP0003607
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm1Jni>/Stat5b<tm1Jni>"	involves: 129 * C57BL/6	MP:0005462	abnormal mast cell differentiation	CCO:MP0005462
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm1Jni>/Stat5b<tm1Jni>"	involves: 129 * C57BL/6	MP:0002423	abnormal mast cell physiology	CCO:MP0002423
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm1Jni>/Stat5b<tm1Jni>"	involves: 129 * C57BL/6	MP:0000336	decreased mast cell number	CCO:MP0000336
MGI:103036	Stat5a	Stat5a/Stat5b<tm2.1Mam>/Stat5a/Stat5b<tm2.1Mam>	involves: 129S6/SvEvTac * Black Swiss	MP:0001577	anemia	CCO:MP0001577
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0000219	increased neutrophil cell number	CCO:MP0000219
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001926	female infertility	CCO:MP0001926
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0000609	abnormal liver physiology	CCO:MP0000609
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001601	abnormal myelopoiesis	CCO:MP0001601
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0002680	decreased corpora lutea number	CCO:MP0002680
MGI:103036	Stat5a	Stat5a<tm1Jni>/Stat5a<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001881	abnormal mammary gland physiology	CCO:MP0001881
MGI:103036	Stat5a	Stat5a<tm1Jni>/Stat5a<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0005334	abnormal fat pad morphology	CCO:MP0005334
MGI:103036	Stat5a	Stat5a/Stat5b<tm2.1Mam>/Stat5a/Stat5b<tm2.1Mam>	involves: 129S6/SvEvTac * Black Swiss	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:103036	Stat5a	"Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0009506	abnormal mammary gland alveolus morphology	CCO:MP0009506
MGI:103036	Stat5a	"Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0009504	abnormal mammary gland epithelium morphology	CCO:MP0009504
MGI:103036	Stat5a	"Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0003838	abnormal milk ejection	CCO:MP0003838
MGI:103036	Stat5a	"Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:103036	Stat5a	Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>	involves: 129S6/SvEvTac * Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:103036	Stat5a	Stat5a<tm1Jni>/Stat5a<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0005334	abnormal fat pad morphology	CCO:MP0005334
MGI:103036	Stat5a	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0005070	impaired NK cell cytolysis	CCO:MP0005070
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0000609	abnormal liver physiology	CCO:MP0000609
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0001261	obese	CCO:MP0001261
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0001262	decreased body weight	CCO:MP0001262
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0000603	pale liver	CCO:MP0000603
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0000416	sparse hair	CCO:MP0000416
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0001882	abnormal lactation	CCO:MP0001882
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0000599	enlarged liver	CCO:MP0000599
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0002619	abnormal lymphocyte morphology	CCO:MP0002619
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0002407	abnormal double-negative T cell morphology	CCO:MP0002407
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0008045	decreased NK cell number	CCO:MP0008045
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0000717	abnormal lymphocyte cell number	CCO:MP0000717
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0002225	abnormal spleen cellularity	CCO:MP0002225
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0004701	decreased circulating insulin-like growth factor I level	CCO:MP0004701
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0002073	abnormal hair growth	CCO:MP0002073
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0004244	abnormal spontaneous abortion rate	CCO:MP0004244
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0005454	decreased adipose tissue amount	CCO:MP0005454
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0001757	abnormal urine chemistry	CCO:MP0001757
MGI:103035	Stat5b	Stat5b<tm1Hwd>/Stat5b<tm1Hwd>	involves: 129 * BALB/c	MP:0005123	increased circulating growth hormone level	CCO:MP0005123
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm1Jni>/Stat5b<tm1Jni>"	involves: 129 * C57BL/6	MP:0005462	abnormal mast cell differentiation	CCO:MP0005462
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm1Jni>/Stat5b<tm1Jni>"	involves: 129 * C57BL/6	MP:0002423	abnormal mast cell physiology	CCO:MP0002423
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm1Jni>/Stat5b<tm1Jni>"	involves: 129 * C57BL/6	MP:0000336	decreased mast cell number	CCO:MP0000336
MGI:103035	Stat5b	Stat5b<tm1Jni>/Stat5b<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0005334	abnormal fat pad morphology	CCO:MP0005334
MGI:103035	Stat5b	Stat5b<tm1Jni>/Stat5b<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0000609	abnormal liver physiology	CCO:MP0000609
MGI:103035	Stat5b	Stat5b<tm1Jni>/Stat5b<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:103035	Stat5b	Stat5b<tm1Jni>/Stat5b<tm1Jni>	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001881	abnormal mammary gland physiology	CCO:MP0001881
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001926	female infertility	CCO:MP0001926
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0000609	abnormal liver physiology	CCO:MP0000609
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001262	decreased body weight	CCO:MP0001262
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0005334	abnormal fat pad morphology	CCO:MP0005334
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0001601	abnormal myelopoiesis	CCO:MP0001601
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0000219	increased neutrophil cell number	CCO:MP0000219
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0000221	decreased leukocyte cell number	CCO:MP0000221
MGI:103035	Stat5b	Stat5a/Stat5b<tm2.1Mam>/Stat5a/Stat5b<tm2.1Mam>	involves: 129S6/SvEvTac * Black Swiss	MP:0001577	anemia	CCO:MP0001577
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0002680	decreased corpora lutea number	CCO:MP0002680
MGI:103035	Stat5b	Stat5a/Stat5b<tm2.1Mam>/Stat5a/Stat5b<tm2.1Mam>	involves: 129S6/SvEvTac * Black Swiss	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:103035	Stat5b	"Stat5a<tm1Jni>/Stat5a<tm1Jni>,Stat5b<tm2Jni>/Stat5b<tm2Jni>"	either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ)	MP:0005018	decreased T cell number	CCO:MP0005018
MGI:103035	Stat5b	"Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0009506	abnormal mammary gland alveolus morphology	CCO:MP0009506
MGI:103035	Stat5b	"Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>,Tg(Wap-cre)11738Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0009504	abnormal mammary gland epithelium morphology	CCO:MP0009504
MGI:103035	Stat5b	"Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0003838	abnormal milk ejection	CCO:MP0003838
MGI:103035	Stat5b	"Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * Black Swiss	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:103035	Stat5b	Stat5a/Stat5b<tm2Mam>/Stat5a/Stat5b<tm2Mam>	involves: 129S6/SvEvTac * Black Swiss	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0008388	hypochromic microcytic anemia	CCO:MP0008388
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0006349	decreased circulating copper level	CCO:MP0006349
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0002641	anisopoikilocytosis	CCO:MP0002641
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0005637	abnormal iron homeostasis	CCO:MP0005637
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0005097	polychromatophilia	CCO:MP0005097
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0008807	increased liver iron level	CCO:MP0008807
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0002874	decreased hemoglobin content	CCO:MP0002874
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0003066	increased liver copper level	CCO:MP0003066
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0003656	abnormal erythrocyte physiology	CCO:MP0003656
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0000274	enlarged heart	CCO:MP0000274
MGI:1915678	Steap3	Steap3<fred>/Steap3<fred>	C57BL/6-Steap3<fred>	MP:0002640	reticulocytosis	CCO:MP0002640
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0005642	decreased mean corpuscular hemoglobin concentration	CCO:MP0005642
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0005637	abnormal iron homeostasis	CCO:MP0005637
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0005562	decreased mean corpuscular hemoglobin	CCO:MP0005562
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002874	decreased hemoglobin content	CCO:MP0002874
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002641	anisopoikilocytosis	CCO:MP0002641
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0008807	increased liver iron level	CCO:MP0008807
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0003131	increased erythrocyte cell number	CCO:MP0003131
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0005637	abnormal iron homeostasis	CCO:MP0005637
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0005505	increased platelet cell number	CCO:MP0005505
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002874	decreased hemoglobin content	CCO:MP0002874
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002424	abnormal reticulocyte morphology	CCO:MP0002424
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002640	reticulocytosis	CCO:MP0002640
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0003131	increased erythrocyte cell number	CCO:MP0003131
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0005562	decreased mean corpuscular hemoglobin	CCO:MP0005562
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002591	decreased mean corpuscular volume	CCO:MP0002591
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002640	reticulocytosis	CCO:MP0002640
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002124	abnormal red blood cell	CCO:MP0002124
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0008807	increased liver iron level	CCO:MP0008807
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0000208	decreased hematocrit	CCO:MP0000208
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002591	decreased mean corpuscular volume	CCO:MP0002591
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002424	abnormal reticulocyte morphology	CCO:MP0002424
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002447	abnormal erythrocyte morphology	CCO:MP0002447
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002124	abnormal red blood cell	CCO:MP0002124
MGI:1915678	Steap3	Steap3<tm1Mdf>/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0002641	anisopoikilocytosis	CCO:MP0002641
MGI:1915678	Steap3	Del(1)1Brk/Steap3<tm1Mdf>	involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6J * CBA/J	MP:0005642	decreased mean corpuscular hemoglobin concentration	CCO:MP0005642
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0001190	reddish skin	CCO:MP0001190
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0004255	abnormal spongiotrophoblast layer morphology	CCO:MP0004255
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<tm1.2Rdp>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0001712	abnormal placenta development	CCO:MP0001712
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<tm1.2Rdp>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0001622	abnormal vasculogenesis	CCO:MP0001622
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0006381	hamartoma	CCO:MP0006381
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0003270	intestinal obstruction	CCO:MP0003270
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0001663	abnormal digestive system physiology	CCO:MP0001663
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0000462	abnormal digestive system morphology	CCO:MP0000462
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<tm1.2Rdp>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0001700	abnormal embryo turning	CCO:MP0001700
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<tm1.2Rdp>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0001719	absent vitelline blood vessels	CCO:MP0001719
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0002825	abnormal notochord morphology	CCO:MP0002825
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0005592	abnormal vascular smooth muscle morphology	CCO:MP0005592
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0003231	abnormal placenta vasculature	CCO:MP0003231
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<+>,Tagln<tm1(cre/ESR1)Feil>/Tagln<+>"	involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0000462	abnormal digestive system morphology	CCO:MP0000462
MGI:1341870	Stk11	Stk11<tm1.1Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * SJL	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0009145	abnormal pancreatic acinus morphology	CCO:MP0009145
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0003809	abnormal hair shaft morphology	CCO:MP0003809
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0001314	corneal opacity	CCO:MP0001314
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0000410	waved hair	CCO:MP0000410
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0000422	delayed hair appearance	CCO:MP0000422
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0001265	decreased body size	CCO:MP0001265
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0002076	abnormal hair follicle structure/orientation	CCO:MP0002076
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0009181	decreased pancreatic delta cell number	CCO:MP0009181
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0009177	decreased pancreatic alpha cell number	CCO:MP0009177
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<tm1.2Rdp>	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0009146	abnormal pancreatic acinar cell morphology	CCO:MP0009146
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0004259	small placenta	CCO:MP0004259
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0004247	small pancreas	CCO:MP0004247
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0003339	decreased pancreatic beta cell number	CCO:MP0003339
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0003334	pancreas fibrosis	CCO:MP0003334
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0005559	increased circulating glucose level	CCO:MP0005559
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0005292	improved glucose tolerance	CCO:MP0005292
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0005215	abnormal pancreatic islet morphology	CCO:MP0005215
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0005220	abnormal exocrine pancreas morphology	CCO:MP0005220
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0001869	pancreas inflammation	CCO:MP0001869
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(Pdx1-cre)89.1Dam/0"	involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR	MP:0009172	small pancreatic islets	CCO:MP0009172
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0004868	endometrial carcinoma	CCO:MP0004868
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0003720	abnormal neural tube closure	CCO:MP0003720
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0009656	delayed chorioallantoic fusion	CCO:MP0009656
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0001270	distended abdomen	CCO:MP0001270
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0002083	premature death	CCO:MP0002083
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0002947	hemangioma	CCO:MP0002947
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0003299	gastric polyps	CCO:MP0003299
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0003270	intestinal obstruction	CCO:MP0003270
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0003271	abnormal duodenum morphology	CCO:MP0003271
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0006337	abnormal first branchial arch morphology	CCO:MP0006337
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0006301	abnormal mesenchyme morphology	CCO:MP0006301
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	involves: 129S7/SvEvBrd * C57BL/6 * CD-1	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	involves: 129S7/SvEvBrd * C57BL/6 * CD-1	MP:0003299	gastric polyps	CCO:MP0003299
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	involves: 129S7/SvEvBrd * C57BL/6 * CD-1	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:1341870	Stk11	"Ptgs2<tm1Jed>/Ptgs2<tm1Jed>,Stk11<tm1Tpm>/Stk11<+>"	involves: 129S7/SvEvBrd * C57BL/6 * CD-1	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:1341870	Stk11	"Ptgs2<tm1Jed>/Ptgs2<tm1Jed>,Stk11<tm1Tpm>/Stk11<+>"	involves: 129S7/SvEvBrd * C57BL/6 * CD-1	MP:0003299	gastric polyps	CCO:MP0003299
MGI:1341870	Stk11	"Ptgs2<tm1Jed>/Ptgs2<tm1Jed>,Stk11<tm1Tpm>/Stk11<+>"	involves: 129S7/SvEvBrd * C57BL/6 * CD-1	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:1341870	Stk11	"Ptgs2<tm1Jed>/Ptgs2<+>,Stk11<tm1Tpm>/Stk11<+>"	involves: 129S7/SvEvBrd * C57BL/6 * CD-1	MP:0003299	gastric polyps	CCO:MP0003299
MGI:1341870	Stk11	"Ptgs2<tm1Jed>/Ptgs2<+>,Stk11<tm1Tpm>/Stk11<+>"	involves: 129S7/SvEvBrd * C57BL/6 * CD-1	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<+>	Not Specified	MP:0003324	liver adenoma	CCO:MP0003324
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0002825	abnormal notochord morphology	CCO:MP0002825
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0004787	abnormal dorsal aorta morphology	CCO:MP0004787
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0004837	abnormal neural fold formation	CCO:MP0004837
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0006301	abnormal mesenchyme morphology	CCO:MP0006301
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0006337	abnormal first branchial arch morphology	CCO:MP0006337
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0006342	absent first branchial arch	CCO:MP0006342
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0008803	abnormal placental labyrinth vasculature morphology	CCO:MP0008803
MGI:1341870	Stk11	Stk11<tm1Tpm>/Stk11<tm1Tpm>	Not Specified	MP:0009656	delayed chorioallantoic fusion	CCO:MP0009656
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0001711	abnormal placenta morphology	CCO:MP0001711
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0006342	absent first branchial arch	CCO:MP0006342
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0001719	absent vitelline blood vessels	CCO:MP0001719
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0003231	abnormal placenta vasculature	CCO:MP0003231
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0005592	abnormal vascular smooth muscle morphology	CCO:MP0005592
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tg(KRT14-cre)1Ipc/0"	involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL	MP:0000416	sparse hair	CCO:MP0000416
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0003720	abnormal neural tube closure	CCO:MP0003720
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0004180	failure of initiation of embryo turning	CCO:MP0004180
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0004255	abnormal spongiotrophoblast layer morphology	CCO:MP0004255
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0004259	small placenta	CCO:MP0004259
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0004787	abnormal dorsal aorta morphology	CCO:MP0004787
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0004837	abnormal neural fold formation	CCO:MP0004837
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<+>,Tagln<tm1(cre/ESR1)Feil>/Tagln<+>"	involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0001663	abnormal digestive system physiology	CCO:MP0001663
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N * SJL	MP:0000462	abnormal digestive system morphology	CCO:MP0000462
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1341870	Stk11	Stk11<tm2.1Tpm>/Stk11<tm2.1Tpm>	involves: BALB/c * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tagln<tm1(cre/ESR1)Feil>/Tagln<+>"	involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1341870	Stk11	Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>	involves: 129S6/SvEvTac * FVB/N	MP:0004868	endometrial carcinoma	CCO:MP0004868
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * FVB/N	MP:0008011	intestinal polyps	CCO:MP0008011
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<+>	involves: 129S6/SvEvTac * FVB/N	MP:0004868	endometrial carcinoma	CCO:MP0004868
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<tm1.1Rdp>,Tagln<tm1(cre/ESR1)Feil>/Tagln<+>"	involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0000462	abnormal digestive system morphology	CCO:MP0000462
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<+>,Tagln<tm1(cre/ESR1)Feil>/Tagln<+>"	involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:1341870	Stk11	"Stk11<tm1.1Rdp>/Stk11<+>,Tagln<tm1(cre/ESR1)Feil>/Tagln<+>"	involves: 129S/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:1341870	Stk11	Stk11<tm1.2Rdp>/Stk11<tm1.2Rdp>	involves: 129S6/SvEvTac	MP:0005076	abnormal cell differentiation	CCO:MP0005076
MGI:1341870	Stk11	Stk11<tm1.1Jish>/Stk11<tm1.1Jish>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001701	incomplete embryo turning	CCO:MP0001701
MGI:1341870	Stk11	Stk11<tm1.1Jish>/Stk11<+>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002815	adenoma	CCO:MP0002815
MGI:1341870	Stk11	Stk11<tm1.1Jish>/Stk11<+>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002404	intestinal adenoma	CCO:MP0002404
MGI:1341870	Stk11	Stk11<tm1.1Jish>/Stk11<tm1.1Jish>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005222	abnormal somite size	CCO:MP0005222
MGI:1341870	Stk11	Stk11<tm1.1Jish>/Stk11<tm1.1Jish>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1341870	Stk11	Stk11<tm1.1Jish>/Stk11<tm1.1Jish>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1341870	Stk11	Stk11<tm1.1Jish>/Stk11<+>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003299	gastric polyps	CCO:MP0003299
MGI:1341870	Stk11	Stk11<tm1.1Jish>/Stk11<tm1.1Jish>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<+>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0001270	distended abdomen	CCO:MP0001270
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0001270	distended abdomen	CCO:MP0001270
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<+>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006381	hamartoma	CCO:MP0006381
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003269	colonic polyps	CCO:MP0003269
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006381	hamartoma	CCO:MP0006381
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<+>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003299	gastric polyps	CCO:MP0003299
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<+>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0000691	enlarged spleen	CCO:MP0000691
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<+>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0000599	enlarged liver	CCO:MP0000599
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<+>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<+>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003883	enlarged stomach	CCO:MP0003883
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<tm1.1Mlfr>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:1341870	Stk11	Stk11<tm1.1Mlfr>/Stk11<+>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0000477	abnormal intestine morphology	CCO:MP0000477
MGI:1341870	Stk11	Stk11<tm1Keis>/Stk11<tm1Keis>	Not Specified	MP:0001925	male infertility	CCO:MP0001925
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003299	gastric polyps	CCO:MP0003299
MGI:1341870	Stk11	Stk11<tm1Keis>/Stk11<tm1Keis>	Not Specified	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:1341870	Stk11	"Stk11<tm1Keis>/Stk11<tm1Keis>,Tg(Ckmm-cre)5Khn/0"	involves: FVB	MP:0001925	male infertility	CCO:MP0001925
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006381	hamartoma	CCO:MP0006381
MGI:1341870	Stk11	"Stk11<tm1Keis>/Stk11<tm1Keis>,Tg(Ckmm-cre)5Khn/0"	involves: FVB	MP:0004130	abnormal muscle cell glucose uptake	CCO:MP0004130
MGI:1341870	Stk11	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0005405	axon degeneration	CCO:MP0005405
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0000751	myopathy	CCO:MP0000751
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0000921	demyelination	CCO:MP0000921
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0005403	abnormal nerve conduction	CCO:MP0005403
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0003632	abnormal nervous system morphology	CCO:MP0003632
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0004883	abnormal blood vessel healing	CCO:MP0004883
MGI:96739	Stmn1	Stmn1<tm1Wed>/Stmn1<tm1Wed>	involves: 129P2/OlaHsd * C57BL/6	MP:0002183	gliosis	CCO:MP0002183
MGI:107917	Stra8	Stra8<tm1Dcp>/Stra8<tm1Dcp>	Not Specified	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:107917	Stra8	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	MP:0004805	absent oocytes	CCO:MP0004805
MGI:107917	Stra8	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	MP:0001132	absent mature ovarian follicles	CCO:MP0001132
MGI:107917	Stra8	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:107917	Stra8	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:107917	Stra8	Stra8<tm1.1Nbg>/Stra8<tm1.1Nbg>	involves: 129S2/SvPas * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1099440	Suv39h1	Suv39h1<tm1Jnw>/Suv39h1<+>	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0001116	small gonad	CCO:MP0001116
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<+>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<+>,Suv39h2<tm1Jnw>/Suv39h2<+>"	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<+>"	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1099440	Suv39h1	Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0001924	infertility	CCO:MP0001924
MGI:1099440	Suv39h1	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1890396	Suv39h2	Suv39h2<tm1Jnw>/Suv39h2<+>	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1890396	Suv39h2	Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0001924	infertility	CCO:MP0001924
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<+>"	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<+>,Suv39h2<tm1Jnw>/Suv39h2<+>"	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<+>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:1890396	Suv39h2	"Suv39h1<tm1Jnw>/Suv39h1<tm1Jnw>,Suv39h2<tm1Jnw>/Suv39h2<tm1Jnw>"	involves: 129 * C57BL/6J	MP:0001116	small gonad	CCO:MP0001116
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002682	decreased mature ovarian follicle number	CCO:MP0002682
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0009452	abnormal synaptonemal complex	CCO:MP0009452
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001127	small ovary	CCO:MP0001127
MGI:1921325	Syce1	Syce1<tm1Hgu>/Syce1<tm1Hgu>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:1919096	Syce2	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:1919096	Syce2	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:1919096	Syce2	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1919096	Syce2	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1919096	Syce2	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	MP:0001127	small ovary	CCO:MP0001127
MGI:1919096	Syce2	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1919096	Syce2	Syce2<Gt(FHCRC-GT-S8-7E1)Sor>/Syce2<Gt(FHCRC-GT-S8-7E1)Sor>	involves: C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0001926	female infertility	CCO:MP0001926
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0004856	decreased ovary weight	CCO:MP0004856
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:105931	Sycp1	Sycp1<tm1Aps>/Sycp1<tm1Aps>	involves: 129P2/OlaHsd * C57BL/6	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001145	abnormal male reproductive system morphology	CCO:MP0001145
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001935	decreased litter size	CCO:MP0001935
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1933281	Sycp2	Sycp2<tm1Jw>/Sycp2<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6NCrl	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6NCrl	MP:0001935	decreased litter size	CCO:MP0001935
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6	MP:0001153	small seminiferous tubules	CCO:MP0001153
MGI:109542	Sycp3	Sycp3<tm1Hoog>/Sycp3<tm1Hoog>	involves: 129P2/OlaHsd * C57BL/6NCrl	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1928899	Tacc2	Tacc2<tm1Jni>/Tacc2<tm1Jni>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0003743	abnormal facial morphology	CCO:MP0003743
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<+>	involves: C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0000163	abnormal cartilage morphology	CCO:MP0000163
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0002114	abnormal axial skeleton morphology	CCO:MP0002114
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0000164	abnormal cartilage development	CCO:MP0000164
MGI:1341163	Tacc3	Tacc3<tm1.1Tno>/Tacc3<tm1.2Tno>	involves: C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0001258	decreased body length	CCO:MP0001258
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0000592	short tail	CCO:MP0000592
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0000076	abnormal calvaria morphology	CCO:MP0000076
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0003794	delayed somite formation	CCO:MP0003794
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0004599	abnormal vertebral arch morphology	CCO:MP0004599
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0004621	lumbar vertebral fusion	CCO:MP0004621
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0008271	abnormal bone ossification	CCO:MP0008271
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0000755	hindlimb paralysis	CCO:MP0000755
MGI:1341163	Tacc3	Tacc3<tm1.1Tno>/Tacc3<tm1.2Tno>	involves: C57BL/6	MP:0004046	abnormal mitosis	CCO:MP0004046
MGI:1341163	Tacc3	Tacc3<tm1.1Tno>/Tacc3<tm1.1Tno>	involves: C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1341163	Tacc3	Tacc3<tm1.2Tno>/Tacc3<tm1.2Tno>	involves: C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1341163	Tacc3	Tacc3<tm1.2Tno>/Tacc3<tm1.2Tno>	involves: C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1.2Tno>	involves: C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1.2Tno>	involves: C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0004653	absent caudal vertebrae	CCO:MP0004653
MGI:1341163	Tacc3	Tacc3<tm1Tno>/Tacc3<tm1Tno>	involves: C57BL/6	MP:0003050	abnormal sacral vertebrae morphology	CCO:MP0003050
MGI:1341163	Tacc3	Tacc3<tm1Jni>/Tacc3<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1341163	Tacc3	Tacc3<tm1Jni>/Tacc3<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	MP:0004810	decreased hematopoietic stem cell number	CCO:MP0004810
MGI:1341163	Tacc3	Tacc3<tm1Jni>/Tacc3<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:1341163	Tacc3	Tacc3<tm1Jni>/Tacc3<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	MP:0002123	abnormal hematopoiesis	CCO:MP0002123
MGI:1341163	Tacc3	Tacc3<tm1Jni>/Tacc3<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1341163	Tacc3	Tacc3<tm1Jni>/Tacc3<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	MP:0000108	midline facial cleft	CCO:MP0000108
MGI:1341163	Tacc3	Tacc3<tm1Jni>/Tacc3<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	MP:0000706	small thymus	CCO:MP0000706
MGI:1341163	Tacc3	Tacc3<tm1Jni>/Tacc3<tm1Jni>	involves: 129P2/OlaHsd * C57BL/6	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:1346320	Taf10	Taf10<tm1.1Lzt>/Taf10<tm1.1Lzt>	involves: 129 * C57BL/6 * SJL	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0003853	dry skin	CCO:MP0003853
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0009608	abnormal lamellar body morphology	CCO:MP0009608
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0001196	shiny skin	CCO:MP0001196
MGI:1346320	Taf10	Taf10<tm1.1Lzt>/Taf10<tm1.1Lzt>	involves: 129 * C57BL/6 * SJL	MP:0005031	abnormal trophoblast layer morphology	CCO:MP0005031
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0002796	impaired skin barrier function	CCO:MP0002796
MGI:1346320	Taf10	Taf10<tm1.1Lzt>/Taf10<tm1.1Lzt>	involves: 129 * C57BL/6 * SJL	MP:0003886	abnormal embryonic epiblast morphology	CCO:MP0003886
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0001429	dehydration	CCO:MP0001429
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:1346320	Taf10	Taf10<tm1.1Lzt>/Taf10<tm1.1Lzt>	involves: 129 * C57BL/6 * SJL	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0001240	abnormal epidermis stratum corneum morphology	CCO:MP0001240
MGI:1346320	Taf10	Taf10<tm1.1Lzt>/Taf10<tm1.1Lzt>	involves: 129 * C57BL/6 * SJL	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1346320	Taf10	Taf10<tm1.1Lzt>/Taf10<tm1.1Lzt>	involves: 129 * C57BL/6 * SJL	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1346320	Taf10	Taf10<tm1.1Lzt>/Taf10<tm1.1Lzt>	involves: 129 * C57BL/6 * SJL	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1346320	Taf10	Taf10<tm1.1Lzt>/Taf10<tm1.1Lzt>	involves: 129 * C57BL/6 * SJL	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0001241	absent epidermis stratum corneum	CCO:MP0001241
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0002656	abnormal keratinocyte differentiation	CCO:MP0002656
MGI:1346320	Taf10	"Taf10<tm1Lzt>/Taf10<tm1Lzt>,Tg(KRT14-cre)1Ipc/0"	involves: 129 * C57BL/6 * SJL	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0000292	distended pericardial sacs	CCO:MP0000292
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0004837	abnormal neural fold formation	CCO:MP0004837
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0002825	abnormal notochord morphology	CCO:MP0002825
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0005221	abnormal rostral-caudal axis patterning	CCO:MP0005221
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0000784	forebrain hypoplasia	CCO:MP0000784
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0000474	abnormal foregut morphology	CCO:MP0000474
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0000274	enlarged heart	CCO:MP0000274
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0002230	abnormal primitive streak formation	CCO:MP0002230
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0000913	abnormal brain development	CCO:MP0000913
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1202876	Tcf7l1	Tcf7l1<tm2Efu>/Tcf7l1<tm2Efu>	involves: 129/Sv * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0005159	azoospermia	CCO:MP0005159
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0006380	abnormal spermatid morphology	CCO:MP0006380
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001155	arrest of spermatogenesis	CCO:MP0001155
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001125	abnormal oocyte morphology	CCO:MP0001125
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:1933218	Tdrd1	Tdrd1<tm1Chum>/Tdrd1<tm1Chum>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:109634	Terf1	Terf1<tm1Tdl>/Terf1<tm1Tdl>	129/Sv	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:109634	Terf1	Terf1<tm1Tdl>/Terf1<tm1Tdl>	129/Sv	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:109634	Terf1	"Terf1<tm1Tdl>/Terf1<tm1Tdl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129/Sv	MP:0002582	disorganized extraembryonic tissue	CCO:MP0002582
MGI:109634	Terf1	Terf1<tm1Tdl>/Terf1<tm1Tdl>	129/Sv	MP:0005032	abnormal ectoplacental cone	CCO:MP0005032
MGI:109634	Terf1	"Terf1<tm1Tdl>/Terf1<tm1Tdl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129/Sv	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:109634	Terf1	Terf1<tm1Tdl>/Terf1<+>	129/Sv	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:109634	Terf1	"Terc<tm1Rdp>/Terc<tm1Rdp>,Terf1<tm1Tdl>/Terf1<tm1Tdl>"	129/Sv	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:109634	Terf1	Terf1<tm1Tdl>/Terf1<tm1Tdl>	129/Sv	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1195972	Terf2	Terf2<tm1.1Tdl>/Terf2<tm1.1Tdl>	involves: 129P2/OlaHsd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1195972	Terf2	"Terf2<tm1Tdl>/Terf2<tm1.1Tdl>,Tg(Mx1-cre)1Cgn/0"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:1195972	Terf2	"Terf2<tm1Tdl>/Terf2<tm1.1Tdl>,Tg(Mx1-cre)1Cgn/0"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA	MP:0000607	abnormal hepatocyte morphology	CCO:MP0000607
MGI:2443298	Tet2	Tet2<Gt(Ayu17-449)Imeg>/Tet2<Gt(Ayu17-449)Imeg>	involves: C57BL/6 * CBA	MP:0004756	abnormal proximal convoluted tubule morphology	CCO:MP0004756
MGI:2443298	Tet2	Tet2<Gt(Ayu17-449)Imeg>/Tet2<Gt(Ayu17-449)Imeg>	involves: C57BL/6 * CBA	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:2443298	Tet2	Tet2<Gt(Ayu17-449)Imeg>/Tet2<Gt(Ayu17-449)Imeg>	involves: C57BL/6 * CBA	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1933237	Tex11	"Tex11<tm1Jw>/Tex11<tm1Jw>,Tg(ACTB-cre)2Mrt/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0001935	decreased litter size	CCO:MP0001935
MGI:1933237	Tex11	"Tex11<tm1Jw>/Y,Tg(ACTB-cre)2Mrt/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0008966	abnormal chiasmata formation	CCO:MP0008966
MGI:1933237	Tex11	"Tex11<tm1Jw>/Y,Tg(ACTB-cre)2Mrt/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:1933237	Tex11	"Tex11<tm1Jw>/Y,Tg(ACTB-cre)2Mrt/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1933237	Tex11	"Tex11<tm1Jw>/Y,Tg(ACTB-cre)2Mrt/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1933237	Tex11	"Tex11<tm1Jw>/Y,Tg(ACTB-cre)2Mrt/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0004218	meiotic nondisjunction during M1 phase	CCO:MP0004218
MGI:1933237	Tex11	"Tex11<tm1Jw>/Tex11<tm1Jw>,Tg(ACTB-cre)2Mrt/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0008966	abnormal chiasmata formation	CCO:MP0008966
MGI:1933237	Tex11	Tex11<tm1.1Jpt>/Y	involves: 129/Sv * C57BL/6 * CD-1	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1933237	Tex11	Tex11<tm1.1Jpt>/Y	involves: 129/Sv * C57BL/6 * CD-1	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:1933237	Tex11	"Tex11<tm1Jw>/Y,Tg(ACTB-cre)2Mrt/0"	involves: 129S4/SvJae * C57BL/6 * FVB/N	MP:0001925	male infertility	CCO:MP0001925
MGI:1934816	Tex15	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:1934816	Tex15	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:1934816	Tex15	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0004901	decreased male germ cell number	CCO:MP0004901
MGI:1934816	Tex15	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1934816	Tex15	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:1934816	Tex15	Tex15<tm1Jw>/Tex15<tm1Jw>	involves: 129S4/SvJae * C57BL/6	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:101934	Tfdp1	Tfdp1<tm1Lili>/Tfdp1<tm1Lili>	involves: 129S2/SvPas * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:101934	Tfdp1	"Tfdp1<tm1Lili>/Tfdp1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000914	exencephaly	CCO:MP0000914
MGI:101934	Tfdp1	Tfdp1<tm1Lili>/Tfdp1<tm1Lili>	involves: 129S2/SvPas * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:101934	Tfdp1	"Tfdp1<tm1Lili>/Tfdp1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:101934	Tfdp1	"Tfdp1<tm1Lili>/Tfdp1<tm1Lili>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:101934	Tfdp1	Tfdp1<tm1Lili>/Tfdp1<tm1Lili>	involves: 129S2/SvPas * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:101934	Tfdp1	Tfdp1<tm1Lili>/Tfdp1<tm1Lili>	involves: 129S2/SvPas * C57BL/6	MP:0002584	small ectoplacental cone	CCO:MP0002584
MGI:101934	Tfdp1	Tfdp1<tm1Lili>/Tfdp1<tm1Lili>	involves: 129S2/SvPas * C57BL/6	MP:0001718	abnormal yolk sac morphology	CCO:MP0001718
MGI:101934	Tfdp1	Tfdp1<tm1Lili>/Tfdp1<tm1Lili>	involves: 129S2/SvPas * C57BL/6	MP:0001713	decreased trophoblast giant cell number	CCO:MP0001713
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129/Sv * 129P2/OlaHsd * Black Swiss * C57BL/6J	MP:0003243	abnormal dopaminergic neuron morphology	CCO:MP0003243
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129/Sv * 129P2/OlaHsd * Black Swiss * C57BL/6J	MP:0005643	decreased dopamine level	CCO:MP0005643
MGI:98726	Tgfb2	"Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>,Tgfb2<tm1Doe>/Tgfb2<tm1Doe>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:98726	Tgfb2	"Cdkn2a<tm1(GFP)Cjs>/Cdkn2a<tm1(GFP)Cjs>,Tgfb2<tm1Doe>/Tgfb2<+>"	involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:98726	Tgfb2	"Cdkn2a<tm1Sxs>/Cdkn2a<+>,Tgfb2<tm1Doe>/Tgfb2<tm1Doe>"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:98726	Tgfb2	"Cdkn2a<tm1Cjs>/Cdkn2a<+>,Tgfb2<tm1Doe>/Tgfb2<tm1Doe>"	involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * C57BL/6	MP:0009621	primary vitreous hyperplasia	CCO:MP0009621
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002451	abnormal macrophage physiology	CCO:MP0002451
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002745	abnormal atrioventricular valve morphology	CCO:MP0002745
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002624	abnormal tricuspid valve morphology	CCO:MP0002624
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002746	abnormal semilunar valve morphology	CCO:MP0002746
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000286	abnormal mitral valve morphology	CCO:MP0000286
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002705	dilated renal tubules	CCO:MP0002705
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000299	failure of endocardial cushion closure	CCO:MP0000299
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000295	poorly developed ventricular trabeculae	CCO:MP0000295
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001954	respiratory distress	CCO:MP0001954
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001575	cyanosis	CCO:MP0001575
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001329	retina hyperplasia	CCO:MP0001329
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002747	abnormal aortic valve morphology	CCO:MP0002747
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002925	abnormal cardiovascular development	CCO:MP0002925
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000076	abnormal calvaria morphology	CCO:MP0000076
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002748	abnormal pulmonary valve morphology	CCO:MP0002748
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002754	dilated heart right ventricle	CCO:MP0002754
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005205	abnormal eye anterior chamber	CCO:MP0005205
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005208	abnormal iris stroma morphology	CCO:MP0005208
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005298	abnormal clavicle morphology	CCO:MP0005298
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005296	abnormal humerus morphology	CCO:MP0005296
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005295	double inlet heart left ventricle	CCO:MP0005295
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005297	spina bifida occulta	CCO:MP0005297
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005300	abnormal corneal stroma morphology	CCO:MP0005300
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000520	absent kidney	CCO:MP0000520
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002855	abnormal cochlear ganglion morphology	CCO:MP0002855
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000559	abnormal femur morphology	CCO:MP0000559
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005543	corneal thinning	CCO:MP0005543
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005329	abnormal cardiac muscle morphology	CCO:MP0005329
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001289	persistence of hyaloid capillary system	CCO:MP0001289
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	MP:0005578	teratozoospermia	CCO:MP0005578
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000111	cleft palate	CCO:MP0000111
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002135	abnormal kidney morphology	CCO:MP0002135
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000639	abnormal adrenal gland morphology	CCO:MP0000639
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002116	abnormal craniofacial bone morphology	CCO:MP0002116
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000431	absent palatine shelf	CCO:MP0000431
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000458	abnormal mandible morphology	CCO:MP0000458
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001262	decreased body weight	CCO:MP0001262
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001940	testicular hypoplasia	CCO:MP0001940
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000157	abnormal sternum morphology	CCO:MP0000157
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000088	short mandible	CCO:MP0000088
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000484	abnormal pulmonary artery morphology	CCO:MP0000484
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001120	abnormal uterus morphology	CCO:MP0001120
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001307	fused cornea and lens	CCO:MP0001307
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000031	abnormal cochlea morphology	CCO:MP0000031
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000154	rib fusion	CCO:MP0000154
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000159	abnormal xiphoid process	CCO:MP0000159
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000085	large anterior fontanelle	CCO:MP0000085
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000272	abnormal aorta morphology	CCO:MP0000272
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000284	double outlet heart right ventricle	CCO:MP0000284
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000297	abnormal endocardial cushion morphology	CCO:MP0000297
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0000150	abnormal rib morphology	CCO:MP0000150
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004384	small interparietal bone	CCO:MP0004384
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0006126	abnormal outflow tract development	CCO:MP0006126
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0003395	abnormal subclavian artery morphology	CCO:MP0003395
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0006200	vitreous body deposition	CCO:MP0006200
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0003958	heart valve hyperplasia	CCO:MP0003958
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004113	abnormal aortic arch morphology	CCO:MP0004113
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004194	abnormal kidney pelvis morphology	CCO:MP0004194
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004282	retrognathia	CCO:MP0004282
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004283	absent corneal endothelium	CCO:MP0004283
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004285	absent Descemet membrane	CCO:MP0004285
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004304	absent spiral limbus	CCO:MP0004304
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004307	absent Rosenthal canal	CCO:MP0004307
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004354	absent deltoid tuberosity	CCO:MP0004354
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004355	short radius	CCO:MP0004355
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0006113	abnormal heart septum morphology	CCO:MP0006113
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004595	abnormal mandibular condyloid process morphology	CCO:MP0004595
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004418	small parietal bone	CCO:MP0004418
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004422	small temporal bone	CCO:MP0004422
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004440	absent occipital bone	CCO:MP0004440
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004454	absent pterygoid process	CCO:MP0004454
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004458	absent alisphenoid bone	CCO:MP0004458
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004359	short ulna	CCO:MP0004359
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004594	abnormal mandibular coronoid process morphology	CCO:MP0004594
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004377	small frontal bone	CCO:MP0004377
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004624	abnormal thoracic cage	CCO:MP0004624
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0001177	atelectasis	CCO:MP0001177
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0005674	abnormal outflow tract septation	CCO:MP0005674
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004627	abnormal trochanter morphology	CCO:MP0004627
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004787	abnormal dorsal aorta morphology	CCO:MP0004787
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004157	interrupted aortic arch	CCO:MP0004157
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004483	absent interdental cells	CCO:MP0004483
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004251	failure of looping morphogenesis	CCO:MP0004251
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0004913	absent mandibular angle	CCO:MP0004913
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	MP:0001169	abnormal bulbourethral gland morphology	CCO:MP0001169
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	MP:0001170	bulbourethral gland hyperplasia	CCO:MP0001170
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	MP:0005304	cystic bulbourethral gland	CCO:MP0005304
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0006107	abnormal atrioventricular canal morphology	CCO:MP0006107
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0006069	abnormal retinal neuronal layer morphology	CCO:MP0006069
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0003168	abnormal scala vestibuli morphology	CCO:MP0003168
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0003092	decreased corneal stroma thickness	CCO:MP0003092
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<tm1Doe>	involves: 129P2/OlaHsd * Black Swiss	MP:0003094	abnormal posterior stroma morphology	CCO:MP0003094
MGI:98726	Tgfb2	Tgfb2<tm1Doe>/Tgfb2<+>	involves: 129P2/OlaHsd * Black Swiss	MP:0005305	coagulating gland hyperplasia	CCO:MP0005305
MGI:1321393	Timeless	Timeless<tm1Rep>/Timeless<tm1Rep>	involves: 129S4/SvJae	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:2684853	Tmprss11a	Tmprss11a<tm1Dgen>/Tmprss11a<tm1Dgen>	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0001127	small ovary	CCO:MP0001127
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0001147	small testis	CCO:MP0001147
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0000585	kinked tail	CCO:MP0000585
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0000592	short tail	CCO:MP0000592
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0001116	small gonad	CCO:MP0001116
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0002777	absent ovarian follicles	CCO:MP0002777
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0001265	decreased body size	CCO:MP0001265
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0001126	abnormal ovary morphology	CCO:MP0001126
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0001924	infertility	CCO:MP0001924
MGI:1916966	Trip13	Trip13<Gt(RRB047)Byg>/Trip13<Gt(RRB047)Byg>	involves: 129P2/OlaHsd * C57BL/6	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:98834	Trp53	"Tcrbe<tm1Che>/Tcrbe<tm1Che>,Tcrd<tm1Mom>/Tcrd<tm1Mom>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0002407	abnormal double-negative T cell morphology	CCO:MP0002407
MGI:98834	Trp53	Trp53<tm1Wahl>/Trp53<tm1Wahl>	involves: 129S4/SvJae	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	Trp53<tm1Wahl>/Trp53<tm1Wahl>	involves: 129S4/SvJae	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	Trp53<tm1Wahl>/Trp53<tm1Wahl>	involves: 129S4/SvJae	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm3Wahl>/Trp53<tm3Wahl>	involves: 129S4/SvJae	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Tcrbe<tm1Che>/Tcrbe<tm1Che>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0002407	abnormal double-negative T cell morphology	CCO:MP0002407
MGI:98834	Trp53	"Tcrbe<tm1Che>/Tcrbe<tm1Che>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0002408	abnormal double-positive T cell morphology	CCO:MP0002408
MGI:98834	Trp53	"Rad51l1<tm1Kmic>/Rad51l1<tm1Kmic>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6J	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:98834	Trp53	"Tcrbe<tm1Che>/Tcrbe<tm1Che>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0001273	decreased metastatic potential	CCO:MP0001273
MGI:98834	Trp53	"Tcrbe<tm1Che>/Tcrbe<tm1Che>,Tcrd<tm1Mom>/Tcrd<tm1Mom>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Tcrbe<tm1Che>/Tcrbe<tm1Che>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005205	abnormal eye anterior chamber	CCO:MP0005205
MGI:98834	Trp53	"Gnl3<Gt(W223E05)Wrst>/Gnl3<Gt(W223E05)Wrst>,Trp53<tm1Tyj>/Trp53<tm5Tyj>"	involves: 129S2/SvPas * 129S4/SvJae	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005205	abnormal eye anterior chamber	CCO:MP0005205
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:98834	Trp53	"Cdkn2c<tm1Bbd>/Cdkn2c<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0005299	abnormal eye posterior chamber	CCO:MP0005299
MGI:98834	Trp53	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:98834	Trp53	"Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129 * C57BL * FVB/N * SJL	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:98834	Trp53	"Ppm1d<tm1Lad>/Ppm1d<tm1Lad>,Tg(IghMyc)22Bri/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129 * C57BL * FVB/N * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tceb3<tm1Aso>/Tceb3<tm1Aso>,Trp53<tm1Sia>/Trp53<tm1Sia>"	involves: 129S/SvEv * C57BL/6 * CBA	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:98834	Trp53	"Tceb3<tm1Aso>/Tceb3<tm1Aso>,Trp53<tm1Sia>/Trp53<tm1Sia>"	involves: 129S/SvEv * C57BL/6 * CBA	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Tceb3<tm1Aso>/Tceb3<tm1Aso>,Trp53<tm1Sia>/Trp53<tm1Sia>"	involves: 129S/SvEv * C57BL/6 * CBA	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<tm2Brn>,Rbl1<tm1Tyj>/Rbl1<tm1Tyj>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Chx10-EGFP/cre,-ALPP)2Clc/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006310	retinoblastoma	CCO:MP0006310
MGI:98834	Trp53	"Rbbp6<tm1Xya>/Rbbp6<tm1Xya>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:98834	Trp53	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:98834	Trp53	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:98834	Trp53	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0001688	abnormal somite development	CCO:MP0001688
MGI:98834	Trp53	"Kat2a<tm1Roth>/Kat2a<tm1Roth>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0001700	abnormal embryo turning	CCO:MP0001700
MGI:98834	Trp53	"Braf<tm1Mmcm>/Braf<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0008014	lung tumor	CCO:MP0008014
MGI:98834	Trp53	"Cdkn2c<tm1Bbd>/Cdkn2c<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Braf<tm1Mmcm>/Braf<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0001175	abnormal lung morphology	CCO:MP0001175
MGI:98834	Trp53	"Gnl3<Gt(W223E05)Wrst>/Gnl3<Gt(W223E05)Wrst>,Trp53<tm1Tyj>/Trp53<tm5Tyj>"	involves: 129S2/SvPas * 129S4/SvJae	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:98834	Trp53	"Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	MP:0009508	mammary gland ductal carcinoma	CCO:MP0009508
MGI:98834	Trp53	"Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	MP:0000621	salivary adenocarcinoma	CCO:MP0000621
MGI:98834	Trp53	"Brca1<tm1Aash>/Brca1<tm1Aash>,Trp53<tm1Brd>/Trp53<+>,Tg(LGB-cre)74Acl/0"	involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:98834	Trp53	"Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Trp53<tm1Brn>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Cdkn2c<tm1Bbd>/Cdkn2c<tm1Bbd>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Braf<tm1Mmcm>/Braf<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:98834	Trp53	"Suds3<tm1.1Rdp>/Suds3<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6 * FVB	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:98834	Trp53	"Gnl3<Gt(W223E05)Wrst>/Gnl3<Gt(W223E05)Wrst>,Trp53<tm1Tyj>/Trp53<tm5Tyj>"	involves: 129S2/SvPas * 129S4/SvJae	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:98834	Trp53	Trp53<tm5Tyj>/Trp53<tm5Tyj>	involves: 129S4/SvJae	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	Trp53<tm1Mok>/Trp53<+>	involves: 129S/SvEv * C57BL/6	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Gt(ROSA)26Sor<tm1(cre/ESR1)Tyj>/?,Trp53<tm5Tyj>/Trp53<tm5Tyj>"	involves: 129S4/SvJae * C57BL/6	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:98834	Trp53	"Ryr2<tm1Nobs>/Ryr2<tm1Nobs>,Trp53<tm1Sia>/Trp53<+>"	involves: 129X1/SvJ * C57BL/6 * CBA	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Ryr2<tm1Nobs>/Ryr2<tm1Nobs>,Trp53<tm1Sia>/Trp53<+>"	involves: 129X1/SvJ * C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Ryr2<tm1Nobs>/Ryr2<tm1Nobs>,Trp53<tm1Sia>/Trp53<tm1Sia>"	involves: 129X1/SvJ * C57BL/6 * CBA	MP:0004511	muscle inflammation	CCO:MP0004511
MGI:98834	Trp53	Trp53<tm3Wahl>/Trp53<tm3Wahl>	involves: 129S4/SvJae	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Ryr2<tm1Nobs>/Ryr2<tm1Nobs>,Trp53<tm1Sia>/Trp53<tm1Sia>"	involves: 129X1/SvJ * C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm3Wahl>/Trp53<tm3Wahl>	involves: 129S4/SvJae	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:98834	Trp53	"Suds3<tm1.1Rdp>/Suds3<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6 * FVB	MP:0004024	aneuploidy	CCO:MP0004024
MGI:98834	Trp53	"Suds3<tm1.1Rdp>/Suds3<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6 * FVB	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Ddb1<tm1Spg>/Ddb1<tm1Spg>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0003237	abnormal lens epithelium morphology	CCO:MP0003237
MGI:98834	Trp53	"Ddb1<tm1Spg>/Ddb1<tm1Spg>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:98834	Trp53	"Ddb1<tm1Spg>/Ddb1<tm1Spg>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0002152	abnormal brain morphology	CCO:MP0002152
MGI:98834	Trp53	Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:98834	Trp53	"Brca1<tm1Brn>/Brca1<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	"Ryr2<tm1Nobs>/Ryr2<tm1Nobs>,Trp53<tm1Sia>/Trp53<tm1Sia>"	involves: 129X1/SvJ * C57BL/6 * CBA	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S5/SvEvBrd	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:98834	Trp53	"Fos<tm1Wag>/Fos<tm1Wag>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Fos<tm1Wag>/Fos<tm1Wag>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Fos<tm1Wag>/Fos<tm1Wag>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000067	osteopetrosis	CCO:MP0000067
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Wrn<tm1Lgu>/Wrn<tm1Lgu>"	involves: 129S2/SvPas * BALB/c	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:98834	Trp53	"Ing1<Gt(OST206270)Lex>/Ing1<Gt(OST206270)Lex>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S5/SvEvBrd	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:98834	Trp53	Trp53<tm3Wahl>/Trp53<tm3Wahl>	involves: 129S4/SvJae	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S5/SvEvBrd	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Dp(4D4Mit190-D4Mit51)1AAM/+,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd	MP:0001265	decreased body size	CCO:MP0001265
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S5/SvEvBrd	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	"Mdm2<tm1Glo>/Mdm2<+>,Mdm4<Gt(VICTR20)7Lex>/Mdm4<+>,Trp53<tm3Wahl>/Trp53<tm3Wahl>"	involves: 129	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Mdm2<tm1Glo>/Mdm2<+>,Trp53<tm3Wahl>/Trp53<tm3Wahl>"	involves: 129S4/SvJae * 129S7/SvEvBrd	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm3Wahl>/Trp53<tm3Wahl>"	involves: 129S4/SvJae * 129S5/SvEvBrd	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm3Wahl>/Trp53<tm3Wahl>"	involves: 129S4/SvJae * 129S5/SvEvBrd	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:98834	Trp53	"Mdm2<tm1Glo>/Mdm2<tm1Glo>,Trp53<tm3Wahl>/Trp53<tm3Wahl>"	involves: 129S4/SvJae * 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	Trp53<tm3Wahl>/Trp53<tm3Wahl>	involves: 129S4/SvJae	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S5/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<+>,Tg(KRT14-rtTA)208Jek/0,Tg(tetO-KLF4)32831Rup/0"	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6NTac * SJL	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:98834	Trp53	Trp53<tm2Wahl>/Trp53<tm2Wahl>	involves: 129S4/SvJae * C57BL/6	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm3Glo>/Trp53<+>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * C57BL/6 * FVB * ICR	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm3Glo>/Trp53<+>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * C57BL/6 * FVB * ICR	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm3Glo>/Trp53<+>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * C57BL/6 * FVB * ICR	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm3Glo>/Trp53<+>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * C57BL/6 * FVB * ICR	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<In(11Trp53;11Wnt3)8Brd>/Trp53<In(11Trp53;11Wnt3)8Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005409	darkened coat color	CCO:MP0005409
MGI:98834	Trp53	Trp53<In(11Trp53;11Wnt3)8Brd>/Trp53<In(11Trp53;11Wnt3)8Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm3Glo>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * FVB * ICR	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<+>,Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0"	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6NTac * SJL	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm3Glo>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * FVB * ICR	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(KRT14-rtTA)208Jek/Y,Tg(tetO-KLF4)32831Rup/0"	involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6NTac * SJL	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:98834	Trp53	"Tg(MMTV-KLF4)1Rup/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6NTac * FVB/NJ * SJL	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Tg(MMTV-KLF4)1Rup/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6NTac * FVB/NJ * SJL	MP:0001212	skin lesions	CCO:MP0001212
MGI:98834	Trp53	"Tg(MMTV-KLF4)1Rup/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6NTac * FVB/NJ * SJL	MP:0001243	abnormal dermal layer morphology	CCO:MP0001243
MGI:98834	Trp53	"Tg(MMTV-KLF4)1Rup/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6NTac * FVB/NJ * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(MMTV-KLF4)1Rup/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6NTac * FVB/NJ * SJL	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:98834	Trp53	Trp53<tm1Att>/Trp53<tm1Att>	Not Specified	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	Trp53<In(11Trp53;11Wnt3)8Brd>/Trp53<In(11Trp53;11Wnt3)8Brd>	129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7-Trp53<tm3.1Glo>	MP:0008057	abnormal DNA replication	CCO:MP0008057
MGI:98834	Trp53	"Ptch1<tm1Mps>/Ptch1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129 * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Ptch1<tm1Mps>/Ptch1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129 * 129S2/SvPas * C57BL/6	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Ptch1<tm1Mps>/Ptch1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129 * 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Sufu<Gt(XB699)Byg>/Sufu<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Sufu<Gt(XB699)Byg>/Sufu<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Sufu<Gt(XB699)Byg>/Sufu<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Sufu<Gt(XB699)Byg>/Sufu<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * FVB * ICR	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Atf4<tm1Jml>/Atf4<tm1Jml>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * 129X1/SvJ	MP:0001303	abnormal lens morphology	CCO:MP0001303
MGI:98834	Trp53	Trp53<tm1Att>/Trp53<tm1Att>	Not Specified	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7-Trp53<tm3.1Glo>	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7-Trp53<tm3.1Glo>	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7-Trp53<tm3.1Glo>	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<tm3.1Glo>	B6.129S7-Trp53<tm3.1Glo>	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm3.1Glo>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * FVB * ICR	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT5-cre/PGR)1Der/?"	involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * FVB * ICR	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:98834	Trp53	"Atf4<tm1Jml>/Atf4<tm1Jml>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * 129X1/SvJ	MP:0002840	abnormal lens fiber morphology	CCO:MP0002840
MGI:98834	Trp53	"Suprmam1<BALB/cMed>/Suprmam1<BALB/cMed>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * BALB/cMed * C57BL/6 * C57BL/6J	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Trp53<tm1.1Brn>/Trp53<tm1.1Brn>,Tg(KRT14-cre)8Brn/?"	involves: 129P2/OlaHsd * FVB/N * SKH1	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Trp53<tm1.1Brn>/Trp53<tm1.1Brn>,Tg(KRT14-cre)8Brn/?"	involves: 129P2/OlaHsd * FVB/N * SKH1	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Trp53<tm1.1Brn>/Trp53<tm3Tyj>,Tg(KRT14-cre)8Brn/?"	involves: 129P2/OlaHsd * 129S4/SvJae * FVB/N * SKH1	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Trp53<tm1.1Brn>/Trp53<tm3Tyj>,Tg(KRT14-cre)8Brn/?"	involves: 129P2/OlaHsd * 129S4/SvJae * FVB/N * SKH1	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Trp53<tm1.1Brn>/Trp53<tm3Tyj>,Tg(KRT14-cre)8Brn/?"	involves: 129P2/OlaHsd * 129S4/SvJae * FVB/N * SKH1	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Trp53<tm3Tyj>/Trp53<+>,Tg(KRT14-cre)8Brn/?"	involves: 129S4/SvJae * FVB/N * SKH1	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Trp53<tm3Tyj>/Trp53<+>,Tg(KRT14-cre)8Brn/?"	involves: 129S4/SvJae * FVB/N * SKH1	MP:0002947	hemangioma	CCO:MP0002947
MGI:98834	Trp53	Trp53<tm1Att>/Trp53<tm1Att>	Not Specified	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:98834	Trp53	"Trp53<tm3Tyj>/Trp53<+>,Tg(KRT14-cre)8Brn/?"	involves: 129S4/SvJae * FVB/N * SKH1	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae * SKH1	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Mdm2<tm1Bay>/Mdm2<tm1Mep>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:98834	Trp53	"Mdm2<tm1Bay>/Mdm2<tm1Mep>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002398	abnormal bone marrow cell morphology/development	CCO:MP0002398
MGI:98834	Trp53	"Mdm2<tm1Bay>/Mdm2<tm1Mep>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0000496	abnormal small intestine morphology	CCO:MP0000496
MGI:98834	Trp53	"Dp(4D4Mit190-D4Mit51)1AAM/+,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:98834	Trp53	"Dp(4D4Mit190-D4Mit51)1AAM/+,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd	MP:0001393	ataxia	CCO:MP0001393
MGI:98834	Trp53	"Dp(4D4Mit190-D4Mit51)1AAM/+,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:98834	Trp53	Trp53<tm5Tyj>/Trp53<tm5Tyj>	involves: 129S4/SvJae	MP:0000313	abnormal cell death	CCO:MP0000313
MGI:98834	Trp53	"Trp53<tm3Tyj>/Trp53<+>,Tg(KRT14-cre)8Brn/?"	involves: 129S4/SvJae * FVB/N * SKH1	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0008014	lung tumor	CCO:MP0008014
MGI:98834	Trp53	"Dp(4D4Mit190-D4Mit51)1AAM/+,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:98834	Trp53	Trp53<tm1Att>/Trp53<tm1Att>	Not Specified	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S4/SvJae	MP:0009308	adenocarcinoma	CCO:MP0009308
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S4/SvJae	MP:0008014	lung tumor	CCO:MP0008014
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm3Tyj>/Trp53<+>"	involves: 129S4/SvJae	MP:0008014	lung tumor	CCO:MP0008014
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm2Tyj>"	involves: 129P2/OlaHsd * 129S4/SvJae	MP:0009308	adenocarcinoma	CCO:MP0009308
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm2Tyj>"	involves: 129P2/OlaHsd * 129S4/SvJae	MP:0008014	lung tumor	CCO:MP0008014
MGI:98834	Trp53	"Trp53<tm1.1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/?"	involves: 129P2/OlaHsd * FVB/N * SKH1	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0009308	adenocarcinoma	CCO:MP0009308
MGI:98834	Trp53	"Trp53<tm1.1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/?"	involves: 129P2/OlaHsd * FVB/N * SKH1	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0002048	lung adenoma	CCO:MP0002048
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<+>"	involves: 129P2/OlaHsd	MP:0008014	lung tumor	CCO:MP0008014
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm1Brn>/Trp53<+>"	involves: 129P2/OlaHsd	MP:0002048	lung adenoma	CCO:MP0002048
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae * SKH1	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	Trp53<tm1Att>/Trp53<tm1Att>	Not Specified	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Kras<tm4Tyj>/Kras<+>,Trp53<tm2Tyj>/Trp53<+>"	involves: 129S4/SvJae	MP:0008014	lung tumor	CCO:MP0008014
MGI:98834	Trp53	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<+>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<+>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:98834	Trp53	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	"Tg(Nes-cre)1Kln/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Tg(Nes-cre)1Kln/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Tg(Nes-cre)1Kln/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc4<tm2.1Fwa>/Xrcc4<tm2Fwa>,Tg(Nes-cre)1Kln/0"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Lig4<tm1Icrf>/Lig4<tm1Icrf>,Trp53<tm1Tyj>/Trp53<+>"	either: (involves: 129P2/OlaHsd * 129S2/SvPas) or (involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0001262	decreased body weight	CCO:MP0001262
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0001262	decreased body weight	CCO:MP0001262
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0005014	increased B cell number	CCO:MP0005014
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc4<tm2.1Fwa>/Xrcc4<tm2Fwa>,Tg(Nes-cre)1Kln/0"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0000439	enlarged skull	CCO:MP0000439
MGI:98834	Trp53	Trp53<tm5Tyj>/Trp53<tm5Tyj>	involves: 129S4/SvJae	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<+>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<+>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0001262	decreased body weight	CCO:MP0001262
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm1Pmc>/Xrcc2<tm1Pmc>"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:98834	Trp53	"Mdm2<tm1Glo>/Mdm2<+>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * C57BL/6J	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<+>,Trp53bp2<tm1Xlu>/Trp53bp2<+>"	involves: 129S2/SvPas * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<+>,Trp53bp2<tm1Xlu>/Trp53bp2<+>"	involves: 129S2/SvPas * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<+>,Trp53bp2<tm1Xlu>/Trp53bp2<tm1Xlu>"	involves: 129S2/SvPas * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Trp53bp2<tm1Xlu>/Trp53bp2<tm1Xlu>"	involves: 129S2/SvPas * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc4<tm2.1Fwa>/Xrcc4<tm2Fwa>,Tg(Nes-cre)1Kln/0"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0000864	abnormal vermis morphology	CCO:MP0000864
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<+>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S5/SvEvBrd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	Trp53<tm2Xu>/Trp53<tm2Xu>	involves: 129S6/SvEvTac	MP:0005095	decreased T cell proliferation	CCO:MP0005095
MGI:98834	Trp53	Trp53<tm1Wahl>/Trp53<tm1Wahl>	involves: C57BL/6	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:98834	Trp53	Trp53<tm1Wahl>/Trp53<tm1Wahl>	involves: C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S5/SvEvBrd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Mdm4<Gt(VICTR20)7Lex>/Mdm4<Gt(VICTR20)7Lex>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S5/SvEvBrd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:98834	Trp53	"Mdm2<tm1Glo>/Mdm2<tm1Glo>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Hipk1<tm1Kho>/Hipk1<tm1Kho>,Hipk2<tm1Kho>/Hipk2<tm1Kho>,Trp53<tm1Mok>/Trp53<+>"	involves: 129S/SvEv * C57BL/6	MP:0000914	exencephaly	CCO:MP0000914
MGI:98834	Trp53	"Mdm2<tm1Glo>/Mdm2<+>,Mdm4<Gt(VICTR20)7Lex>/Mdm4<+>,Trp53<tm1Wahl>/Trp53<tm1Wahl>"	involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Trp53<tm2Xu>/Trp53<tm2Xu>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc4<tm2.1Fwa>/Xrcc4<tm2Fwa>,Tg(Nes-cre)1Kln/0"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:98834	Trp53	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:98834	Trp53	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:98834	Trp53	Trp53<tm2Xu>/Trp53<tm2Xu>	involves: 129S6/SvEvTac	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:98834	Trp53	"Tert<tm1Rdp>/Tert<tm1Rdp>,Trp53<tm1Tyj>/Trp53<+>"	B6.Cg-Trp53<tm1Tyj> Tert<tm1Rdp>	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:98834	Trp53	Trp53<tm2Xu>/Trp53<tm2Xu>	involves: 129S6/SvEvTac	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:98834	Trp53	"Trp53<tm2Xu>/Trp53<tm2Xu>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0001199	thin skin	CCO:MP0001199
MGI:98834	Trp53	"Trp53<tm2Xu>/Trp53<tm2Xu>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0000069	kyphoscoliosis	CCO:MP0000069
MGI:98834	Trp53	"Trp53<tm2Xu>/Trp53<tm2Xu>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:98834	Trp53	"Trp53<tm2Xu>/Trp53<tm2Xu>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S6/SvEvTac	MP:0001265	decreased body size	CCO:MP0001265
MGI:98834	Trp53	"Trp53<tm1Xu>/Trp53<tm1Xu>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S4/SvJae	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:98834	Trp53	Trp53<tm2Xu>/Trp53<tm2Xu>	involves: 129S6/SvEvTac	MP:0006414	decreased T cell apoptosis	CCO:MP0006414
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc4<tm2.1Fwa>/Xrcc4<tm2Fwa>,Tg(Nes-cre)1Kln/0"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * SJL	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:98834	Trp53	"Brca1<tm1Cxd>/Brca1<tm1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:98834	Trp53	"Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002013	pilomatriculoma	CCO:MP0002013
MGI:98834	Trp53	"Metap2<tm1.2Ccr>/Metap2<tm1.2Ccr>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0001651	necrosis	CCO:MP0001651
MGI:98834	Trp53	"Metap2<tm1.2Ccr>/Metap2<tm1.2Ccr>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:98834	Trp53	"Metap2<tm1.2Ccr>/Metap2<tm1.2Ccr>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd	MP:0000343	altered response to myocardial infarction	CCO:MP0000343
MGI:98834	Trp53	Trp53<tm3Xu>/Trp53<tm3Xu>	Not Specified	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:98834	Trp53	"Pot1a<tm1Schg>/Pot1a<tm1.1Schg>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:98834	Trp53	"Lig4<tm1Fwa>/Lig4<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S6/SvEvTac * 129S7/SvEvBrd	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	"Pot1a<tm1Schg>/Pot1a<tm1.1Schg>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:98834	Trp53	"Pax3<Sp>/Pax3<Sp>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL * C57BL/6J * FVB	MP:0000929	open neural tube	CCO:MP0000929
MGI:98834	Trp53	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:98834	Trp53	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0001289	persistence of hyaloid capillary system	CCO:MP0001289
MGI:98834	Trp53	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0003236	abnormal lens capsule morphology	CCO:MP0003236
MGI:98834	Trp53	"Metap2<tm1.2Ccr>/Metap2<tm1.2Ccr>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * FVB/N	MP:0000259	abnormal vascular development	CCO:MP0000259
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002013	pilomatriculoma	CCO:MP0002013
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0003711	pathological neovascularization	CCO:MP0003711
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * BALB/c	MP:0004227	increased cellular sensitivity to ionizing radiation	CCO:MP0004227
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0003711	pathological neovascularization	CCO:MP0003711
MGI:98834	Trp53	"Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:98834	Trp53	"Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Pot1a<tm1Schg>/Pot1a<tm1.1Schg>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:98834	Trp53	"Cdh1<tm1Jjon>/Cdh1<tm1Jjon>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Nf1<tm1Tyj>/?,Nstr2<A/J>/?,Trp53<tm1Tyj>/?"	involves: A/J * C57BL/6J	MP:0005514	increased resistance to tumor development	CCO:MP0005514
MGI:98834	Trp53	"Nf1<tm1Tyj>/?,Nstr1<C57BL/6J>/Nstr1<C57BL/6J>,Trp53<tm1Tyj>/?"	involves: A/J * C57BL/6J	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:98834	Trp53	"Nf1<tm1Tyj>/?,Nstr1<A/J>/?,Trp53<tm1Tyj>/?"	involves: A/J * C57BL/6J	MP:0005514	increased resistance to tumor development	CCO:MP0005514
MGI:98834	Trp53	"Pot1a<tm1Schg>/Pot1a<tm1.1Schg>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0003701	elevated level of sister chromatid exchange	CCO:MP0003701
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<tm1Glo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<+>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129 * C57BL/6	MP:0004906	enlarged uterus	CCO:MP0004906
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:98834	Trp53	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002018	malignant tumors	CCO:MP0002018
MGI:98834	Trp53	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(IghMyc)22Bri/0,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * 129X1/SvJ * C57BL * C57BL/6 * SJL	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<tm1Glo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<tm1Glo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(NES-TVA)12Hev/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129 * C57BL/6 * FVB/N	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:98834	Trp53	"Tg(NES-TVA)12Hev/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129 * C57BL/6 * FVB/N	MP:0009277	brain tumor	CCO:MP0009277
MGI:98834	Trp53	"Kat5<tm1Jwl>/Kat5<+>,Tg(IghMyc)22Bri/0,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL * C57BL/6 * SJL	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	"Kat5<tm1Jwl>/Kat5<+>,Tg(IghMyc)22Bri/0,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S1/Sv * 129X1/SvJ * C57BL * C57BL/6 * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:98834	Trp53	"Mtbp<tm1Glo>/Mtbp<tm1Glo>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:98834	Trp53	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<+>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:98834	Trp53	"Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129 * C57BL/6	MP:0009092	endometrium hyperplasia	CCO:MP0009092
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Tyj>/Trp53<+>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Kat5<tm1Jwl>/Kat5<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Tg(IghMyc)22Bri/0,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * 129X1/SvJ * C57BL * C57BL/6 * SJL	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Ptch1<tm1Mps>/Ptch1<+>,Trp53<tm1Tyj>/Trp53<+>,Tg(Nes-cre)1Kln/0"	involves: 129 * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:98834	Trp53	"Rad51<tm1Hst>/Rad51<tm1Hst>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:98834	Trp53	"Tg(KRT14-Birc5)19Gros/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C3H * C57BL/6 * C57BL/6NCr	MP:0001204	increased resistance to skin irradiation	CCO:MP0001204
MGI:98834	Trp53	"Rad51<tm1Hst>/Rad51<tm1Hst>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0001954	respiratory distress	CCO:MP0001954
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Tg(KRT14-Birc5)19Gros/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C3H * C57BL/6 * C57BL/6NCr	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<+>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Ptch1<tm1Mps>/Ptch1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129 * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0003702	abnormal chromosome morphology	CCO:MP0003702
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Lig4<tm1Pmc>/Lig4<tm1Pmc>,Trp53<tm1Tyj>/Trp53<+>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Brca2<tm1Mak>/Brca2<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Lck-cre)548Jxm/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0001829	increased activated T cell number	CCO:MP0001829
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:98834	Trp53	"Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129 * C57BL/6	MP:0004868	endometrial carcinoma	CCO:MP0004868
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<tm1.1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:98834	Trp53	Trp53<tm1Brn>/Trp53<tm1Brn>	involves: 129P2/OlaHsd * FVB/N	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:98834	Trp53	"Cdca8<tm1Tatn>/Cdca8<tm1Tatn>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL/6 * CBA	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<tm1.1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<tm1.1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<+>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm4Xu>/Trp53<tm4Xu>	Not Specified	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nhej1<tm1Fwa>/Nhej1<tm1Fwa>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Nhej1<tm1Fwa>/Nhej1<tm1Fwa>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	Trp53<tm1.1Brn>/Trp53<tm1.1Brn>	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<tm1.1Cxd>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	"Brca1<tm1Brn>/Brca1<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Brca1<tm1Brn>/Brca1<tm1Brn>,Trp53<tm1Brn>/Trp53<+>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Brca1<tm1Brn>/Brca1<tm1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * BALB/cJ * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(KRT14-cre)8Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<tm1.1Cxd>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<tm1.1Cxd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:98834	Trp53	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Mtbp<tm1Glo>/Mtbp<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002026	leukemia	CCO:MP0002026
MGI:98834	Trp53	Trp53<tm2Holl>/Trp53<tm2Holl>	involves: 129P2/OlaHsd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:98834	Trp53	Trp53<tm1Holl>/Trp53<tm2Holl>	involves: 129P2/OlaHsd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:98834	Trp53	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0001393	ataxia	CCO:MP0001393
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<tm1.1Cxd>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:98834	Trp53	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0001406	abnormal gait	CCO:MP0001406
MGI:98834	Trp53	"Mdm2<tm1Ypz>/Mdm2<tm1Ypz>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6 * FVB/N	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:98834	Trp53	"Nhej1<tm1Fwa>/Nhej1<tm1Fwa>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<+>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<+>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<+>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0002627	teratoma	CCO:MP0002627
MGI:98834	Trp53	"Sirt1<tm1.1Cxd>/Sirt1<+>,Trp53<tm1Brd>/Trp53<+>"	either: (involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB/N)	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:98834	Trp53	"Mtbp<tm1Glo>/Mtbp<tm1Glo>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0002041	pituitary adenoma	CCO:MP0002041
MGI:98834	Trp53	"Dicer1<tm1Snjo>/Dicer1<tm1Snjo>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	"Ppp1r13b<tm1Suda>/Ppp1r13b<tm1Suda>,Trp53<tm1Sia>/Trp53<tm1Sia>"	various	MP:0001879	abnormal lymphatic vessel morphology	CCO:MP0001879
MGI:98834	Trp53	"Glipr1<tm1Tt>/Glipr1<tm1Tt>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Glipr1<tm1Tt>/Glipr1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Tg(MMTV-AURKA)#Cxd/?,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * FVB/N	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Tg(MMTV-AURKA)#Cxd/?,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * FVB/N	MP:0001885	mammary gland duct hyperplasia	CCO:MP0001885
MGI:98834	Trp53	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0000745	tremors	CCO:MP0000745
MGI:98834	Trp53	"Tg(MMTV-AURKA)#Cxd/?,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * FVB/N	MP:0000662	abnormal branching of the mammary ductal tree	CCO:MP0000662
MGI:98834	Trp53	"Pgr<tm2(cre)Lyd>/Pgr<+>,Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129 * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(MMTV-AURKA)#Cxd/?,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * FVB/N	MP:0004025	polyploidy	CCO:MP0004025
MGI:98834	Trp53	"Tg(MMTV-AURKA)#Cxd/?,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * FVB/N	MP:0009504	abnormal mammary gland epithelium morphology	CCO:MP0009504
MGI:98834	Trp53	"Rb1<tm2Brn>/Rb1<tm2Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(Gfap-cre)2Brn/0"	involves: 129P2/OlaHsd * FVB/N	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0001394	circling	CCO:MP0001394
MGI:98834	Trp53	"Rb1<tm2Brn>/Rb1<tm2Brn>,Tg(Gfap-cre)2Brn/0,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * FVB/N	MP:0001525	impaired balance	CCO:MP0001525
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc2<tm2Pmc>/Xrcc2<tm2Pmc>,Tg(Nes-cre)1Kln/0"	involves: 129S2/SvPas * C57BL/6 * SJL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001263	weight loss	CCO:MP0001263
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001244	thin dermal layer	CCO:MP0001244
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Ldo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Ldo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Ldo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Ldo>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002957	intestinal adenocarcinoma	CCO:MP0002957
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000600	liver hypoplasia	CCO:MP0000600
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000160	kyphosis	CCO:MP0000160
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000162	lordosis	CCO:MP0000162
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000423	delayed hair regrowth	CCO:MP0000423
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000416	sparse hair	CCO:MP0000416
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0001327	decreased retinal photoreceptor cell number	CCO:MP0001327
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm5Xu>/Trp53<tm5Xu>	Not Specified	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	B6.129S7-Trp53<tm1Ldo>	MP:0004701	decreased circulating insulin-like growth factor I level	CCO:MP0004701
MGI:98834	Trp53	"Dmbt1<tm1Kumc>/Dmbt1<tm1Kumc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002269	muscular atrophy	CCO:MP0002269
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0004478	testicular teratoma	CCO:MP0004478
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002627	teratoma	CCO:MP0002627
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0001263	weight loss	CCO:MP0001263
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0004478	testicular teratoma	CCO:MP0004478
MGI:98834	Trp53	Trp53<tm1Mlh>/Trp53<tm1Mlh>	involves: 129P2/OlaHsd	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0001940	testicular hypoplasia	CCO:MP0001940
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003446	renal hypoplasia	CCO:MP0003446
MGI:98834	Trp53	"Myst1<tm2Thl>/Myst1<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S1/Sv * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003786	premature aging	CCO:MP0003786
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003918	decreased kidney weight	CCO:MP0003918
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004819	decreased skeletal muscle mass	CCO:MP0004819
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003402	decreased liver weight	CCO:MP0003402
MGI:98834	Trp53	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004953	decreased spleen weight	CCO:MP0004953
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008844	decreased subcutaneous adipose tissue amount	CCO:MP0008844
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0008872	abnormal response to xenobiotics	CCO:MP0008872
MGI:98834	Trp53	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0008515	thin retinal outer nuclear layer	CCO:MP0008515
MGI:98834	Trp53	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0006072	abnormal retinal apoptosis	CCO:MP0006072
MGI:98834	Trp53	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005202	lethargy	CCO:MP0005202
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002627	teratoma	CCO:MP0002627
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	B6.129S7-Trp53<tm1Ldo>	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000063	decreased bone density	CCO:MP0000063
MGI:98834	Trp53	"Cops5<tm1Rpar>/Cops5<tm1Rpar>,Tg(Lck-cre)548Jxm/0,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL	MP:0000715	decreased thymocyte number	CCO:MP0000715
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005051	altered response to anesthetics	CCO:MP0005051
MGI:98834	Trp53	Trp53<tm5Xu>/Trp53<tm5Xu>	Not Specified	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002908	delayed wound healing	CCO:MP0002908
MGI:98834	Trp53	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002092	abnormal eye morphology	CCO:MP0002092
MGI:98834	Trp53	"Brca2<tm1Brn>/Brca2<tm1Brn>,Trp53<tm1Tyj>/Trp53<+>,Tg(Nes-cre)1Kln/0"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0000512	intestinal ulcer	CCO:MP0000512
MGI:98834	Trp53	"Rb1<tm3Tyj>/Rb1<tm3Tyj>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Nes-cre)1Mrt/0"	involves: 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Rb1<tm1.1Jyjw>/Rb1<tm1.1Jyjw>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129S6.129-Trp53<tm1Tyj> Rb1<tm1.1Jyjw>	MP:0001263	weight loss	CCO:MP0001263
MGI:98834	Trp53	Trp53<tm1Ldo>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0000694	spleen hypoplasia	CCO:MP0000694
MGI:98834	Trp53	"Rb1<tm1Brd>/Rb1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0002019	abnormal tumor incidence	CCO:MP0002019
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	NIHOla.129S7-Trp53<tm1Brd>	MP:0004502	decreased incidence of chemically-induced tumors	CCO:MP0004502
MGI:98834	Trp53	"Dmbt1<tm1Kumc>/Dmbt1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	NIHOla.129S7-Trp53<tm1Brd>	MP:0003447	decreased tumor growth/size	CCO:MP0003447
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:98834	Trp53	"Telo2<tm1Tdl>/Telo2<tm1.1Tdl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Gt(ROSA)26Sor<tm1(cre/Esr1)Nat>/Gt(ROSA)26Sor<+>"	involves: 129 * 129P2/OlaHsd * 129S2/SvPas * C57BL/6J	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Cdkn2a<tm1Cjs>/Cdkn2a<tm1Cjs>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * NIH/OlaHsd	MP:0003721	increased tumor growth/size	CCO:MP0003721
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(CMV-cre)1Cgn/0,Trp53<tm2Att>/Trp53<+>"	involves: 129S4/SvJae * BALB/cJ	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Brca1<tm2Mak>/Brca1<tm2Mak>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Wap-cre)11738Mam/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Brca1<tm2Mak>/Brca1<tm2Mak>,Trp53<tm1Brd>/Trp53<+>,Tg(Wap-cre)11738Mam/?"	involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	Trp53<tm2Att>/Trp53<tm2Att>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0008866	chromosomal instability	CCO:MP0008866
MGI:98834	Trp53	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0001429	dehydration	CCO:MP0001429
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0001429	dehydration	CCO:MP0001429
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0001954	respiratory distress	CCO:MP0001954
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0001525	impaired balance	CCO:MP0001525
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>,Xrcc5<tm1Dbr>/Xrcc5<tm1Dbr>"	involves: 129S7/SvEvBrd * C57BL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Rag1<tm1Mom>/Rag1<tm1Mom>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd * C57BL	MP:0001525	impaired balance	CCO:MP0001525
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Brca1<tm2Mak>/Brca1<tm2Mak>,Tg(Lck-cre)548Jxm/?,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6 * CBA	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002048	lung adenoma	CCO:MP0002048
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002014	papilloma	CCO:MP0002014
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	"Ccnd3<tm1Pisc>/Ccnd3<tm1Pisc>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:98834	Trp53	"Fbxw7<tm1Kei>/Fbxw7<tm1Kei>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Lck-cre)1Cwi/?"	involves: 129S2/SvPas * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Fbxw7<tm1Kei>/Fbxw7<tm1Kei>,Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tg(Lck-cre)1Cwi/?"	involves: 129S2/SvPas * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	Trp53<tm1Glo>/Trp53<+>	involves: 129S7/SvEvBrd	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:98834	Trp53	Trp53<tm2Att>/Trp53<tm2Att>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	Trp53<tm2Att>/Trp53<tm2Att>	either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6)	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Kras<tm2Tyj>/Kras<+>,Trp53<tm1Glo>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:98834	Trp53	"Pten<tm1Rdp>/Pten<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(GFAP-cre)25Mes/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0001393	ataxia	CCO:MP0001393
MGI:98834	Trp53	"Brca2<tm1Kamc>/Brca2<tm1Kamc>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:98834	Trp53	"Brca2<tm1Kamc>/Brca2<tm1Kamc>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Brca2<tm1Kamc>/Brca2<tm1Kamc>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	"Tg(S100b-v-erbB)4496Waw/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6J * DBA/2J * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(S100b-v-erbB)4496Waw/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6J * DBA/2J * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Brca2<tm1Kamc>/Brca2<tm1Kamc>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129P2/OlaHsd 129S2/SvPas * BALB/c * C57BL/6	MP:0006079	stomach tumor	CCO:MP0006079
MGI:98834	Trp53	"Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(GFAP-cre)25Mes/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0002018	malignant tumors	CCO:MP0002018
MGI:98834	Trp53	"Pten<tm1Rdp>/Pten<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(GFAP-cre)25Mes/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0002018	malignant tumors	CCO:MP0002018
MGI:98834	Trp53	"Pten<tm1Rdp>/Pten<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(GFAP-cre)25Mes/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0002064	seizures	CCO:MP0002064
MGI:98834	Trp53	"Pten<tm1Rdp>/Pten<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(GFAP-cre)25Mes/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0000753	paralysis	CCO:MP0000753
MGI:98834	Trp53	"Pten<tm1Rdp>/Pten<+>,Trp53<tm1Brn>/Trp53<tm1Brn>,Tg(GFAP-cre)25Mes/0"	involves: 129P2/OlaHsd * C57BL/6 * FVB/N	MP:0008021	blastoma	CCO:MP0008021
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002703	abnormal renal tubule morphology	CCO:MP0002703
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002049	extremity angiosarcoma	CCO:MP0002049
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0004986	abnormal osteoblast morphology	CCO:MP0004986
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002703	abnormal renal tubule morphology	CCO:MP0002703
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0000116	abnormal tooth development	CCO:MP0000116
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	B6.129S2-Trp53<tm1Tyj>/J	MP:0006221	optic nerve hypoplasia	CCO:MP0006221
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0001304	cataracts	CCO:MP0001304
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002035	leiomyosarcoma	CCO:MP0002035
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0001106	abnormal Schwann cell morphology	CCO:MP0001106
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0001304	cataracts	CCO:MP0001304
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)3Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0003580	fibroma	CCO:MP0003580
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0004986	abnormal osteoblast morphology	CCO:MP0004986
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	B6.129S2-Trp53<tm1Tyj>/J	MP:0006219	optic nerve degeneration	CCO:MP0006219
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)2Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002026	leukemia	CCO:MP0002026
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0003570	uterus leiomyoma	CCO:MP0003570
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002026	leukemia	CCO:MP0002026
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0003570	uterus leiomyoma	CCO:MP0003570
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0000599	enlarged liver	CCO:MP0000599
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0003570	uterus leiomyoma	CCO:MP0003570
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<+>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002026	leukemia	CCO:MP0002026
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)3Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:98834	Trp53	"Cdkn2a<tm1.1Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0000599	enlarged liver	CCO:MP0000599
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)3Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)3Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)3Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<+>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)3Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brd>/Trp53<+>,Tg(P0-Cre)3Gth/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * FVB/N	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	B6.129S2-Trp53<tm1Tyj>/J	MP:0002864	abnormal ocular fundus morphology	CCO:MP0002864
MGI:98834	Trp53	"Myf6<tm1(cre)Mrc>/Myf6<+>,Pax3<tm1Mrc>/Pax3<tm1Mrc>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0001525	impaired balance	CCO:MP0001525
MGI:98834	Trp53	"Cdkn2a<tm1.1Brn>/Cdkn2a<+>,Nf2<tm2Gth>/Nf2<tm2Gth>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0000745	tremors	CCO:MP0000745
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0002064	seizures	CCO:MP0002064
MGI:98834	Trp53	"Cobra1<tm1.2Roli>/Cobra1<tm1.2Roli>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S/Sv * C57BL/6 * FVB/N	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:98834	Trp53	"Cobra1<tm1.2Roli>/Cobra1<tm1.2Roli>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S/Sv * C57BL/6 * FVB/N	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:98834	Trp53	"Tg(KRT14-Birc5)19Gros/0,Trp53<tm1Brd>/Trp53<+>"	involves: 129S7/SvEvBrd * C3H * C57BL/6	MP:0004502	decreased incidence of chemically-induced tumors	CCO:MP0004502
MGI:98834	Trp53	"Rag1<tm1Jsek>/Rag1<tm1Jsek>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Rag1<tm1Jsek>/Rag1<tm1Jsek>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	"Rag1<tm1Jsek>/Rag1<tm1Jsek>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0004029	spontaneous chromosome breakage	CCO:MP0004029
MGI:98834	Trp53	"Rag1<tm1Jsek>/Rag1<tm1Jsek>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac	MP:0008770	decreased survivor rate	CCO:MP0008770
MGI:98834	Trp53	"E2f1<tm1Njd>/E2f1<tm1Njd>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S2/SvPas * 129S7/SvEvBrd * SKH1	MP:0001203	increased sensitivity to skin irradiation	CCO:MP0001203
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	B6.129S2-Trp53<tm1Tyj>/J	MP:0002792	abnormal retinal vasculature	CCO:MP0002792
MGI:98834	Trp53	"Tg(KRT14-cre)8Brn/0,Tg(KRT5-Akt1*)Jmpa/0,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Cdkn2a<tm1.1Brn>/Cdkn2a<tm1.1Brn>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Pten<tm1Mro>/Pten<tm1Mro>,Tg(KRT14-cre)8Brn/0,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Pten<tm1Mro>/Pten<tm1Mro>,Tg(KRT14-cre)8Brn/0,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0000746	weakness	CCO:MP0000746
MGI:98834	Trp53	"Pten<tm1Mro>/Pten<tm1Mro>,Tg(KRT14-cre)8Brn/0,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(KRT14-cre)8Brn/0,Tg(KRT5-Akt1*)Jmpa/0,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0009583	increased keratinocyte proliferation	CCO:MP0009583
MGI:98834	Trp53	"Rev3l<tm1Ndew>/Rev3l<tm1Ndew>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:98834	Trp53	"Tg(KRT14-cre)8Brn/0,Tg(KRT5-Akt1*)Jmpa/0,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0003448	altered tumor morphology	CCO:MP0003448
MGI:98834	Trp53	"Rev3l<tm1Ndew>/Rev3l<tm1Ndew>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Tg(KRT14-cre)8Brn/0,Tg(KRT5-Akt1*)Jmpa/0,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	"Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Pten<tm1Hwu>/Pten<tm1Hwu>,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB	MP:0009550	urinary bladder carcinoma	CCO:MP0009550
MGI:98834	Trp53	"Myf6<tm1(cre)Mrc>/Myf6<+>,Pax3<tm1Mrc>/Pax3<tm1Mrc>,Trp53<tm1Brn>/Trp53<+>"	involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Tg(KRT14-cre)8Brn/0,Tg(KRT5-Akt1*)Jmpa/0,Trp53<tm1Brn>/Trp53<tm1Brn>"	involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0002064	seizures	CCO:MP0002064
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	B6.129S2-Trp53<tm1Tyj>/J	MP:0001325	abnormal retina morphology	CCO:MP0001325
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	B6.129S2-Trp53<tm1Tyj>/J	MP:0001330	abnormal optic nerve morphology	CCO:MP0001330
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	129-Trp53<tm1Tyj>/J	MP:0002792	abnormal retinal vasculature	CCO:MP0002792
MGI:98834	Trp53	"Nf1<tm1Fcr>/Nf1<tm1Fcr>,Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S/SvEv * 129S4/SvJae * FVB/N	MP:0009277	brain tumor	CCO:MP0009277
MGI:98834	Trp53	"Nf1<tm1Fcr>/Nf1<tm1Fcr>,Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S/SvEv * 129S4/SvJae * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0009277	brain tumor	CCO:MP0009277
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0005238	increased brain size	CCO:MP0005238
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0001525	impaired balance	CCO:MP0001525
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0001393	ataxia	CCO:MP0001393
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0000745	tremors	CCO:MP0000745
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0001393	ataxia	CCO:MP0001393
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	B6.129S2-Trp53<tm1Tyj>/J	MP:0002700	opacity of vitreous body	CCO:MP0002700
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJae * FVB/N	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Gt(ROSA)26Sor<tm2(sb11)Njen>/Gt(ROSA)26Sor<+>,Trp53<tm3Tyj>/Trp53<+>,Tg(Alb-cre)21Mgn/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	MP:0000598	abnormal liver morphology	CCO:MP0000598
MGI:98834	Trp53	"Gt(ROSA)26Sor<tm2(sb11)Njen>/Gt(ROSA)26Sor<+>,Trp53<tm3Tyj>/Trp53<+>,Tg(Alb-cre)21Mgn/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	MP:0003324	liver adenoma	CCO:MP0003324
MGI:98834	Trp53	"Gt(ROSA)26Sor<tm2(sb11)Njen>/Gt(ROSA)26Sor<+>,Trp53<tm3Tyj>/Trp53<+>,Tg(Alb-cre)21Mgn/0,TgTn(sb-T2/Onc)68Dla/0"	involves: 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0009277	brain tumor	CCO:MP0009277
MGI:98834	Trp53	"Tg(GFAP-cre)25Mes/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * FVB/N	MP:0005238	increased brain size	CCO:MP0005238
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	B6.129S2-Trp53<tm1Tyj>/J	MP:0005195	abnormal posterior eye segment morphology	CCO:MP0005195
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<+>,Trp53bp2<tm1Cdlo>/Trp53bp2<+>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Tfdp1<tm1Lili>/Tfdp1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0000914	exencephaly	CCO:MP0000914
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc1<tm1Rpe>/Xrcc1<tm1Rpe>"	involves: 129X1/SvJ	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc1<tm1Rpe>/Xrcc1<tm1Rpe>"	involves: 129X1/SvJ	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002401	abnormal lymphopoiesis	CCO:MP0002401
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Tfdp1<tm1Lili>/Tfdp1<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc4<tm1Fwa>/Xrcc4<tm1Fwa>"	involves: 129P2/OlaHsd * 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tsg101<tm1Mak>/Tsg101<tm1Mak>"	involves: 129P3/J * C57BL/6 * CD-1	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Dph1<tm2Bhr>/Dph1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Brca1<tm1Cxd>/Brca1<tm2Cxd>,Trp53<tm1Brd>/Trp53<+>,Tg(MMTV-cre)4Mam/0"	involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	"Tfdp1<tm1Lili>/Tfdp1<tm1Lili>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Mdm2<tm1Glo>/Mdm2<tm1Glo>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:98834	Trp53	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Trp53<tm1.1Mok>/Trp53<tm1.1Mok>"	involves: 129S/SvEv * C57BL/6	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Xrcc1<tm1Rpe>/Xrcc1<tm1Rpe>"	involves: 129X1/SvJ	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	Trp53<tm1Sia>/Trp53<tm1Sia>	involves: C57BL/6 * CBA	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0002627	teratoma	CCO:MP0002627
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Sia>/Trp53<tm1Sia>	involves: C57BL/6 * CBA	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Bard1<tm1Thl>/Bard1<tm1Thl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	Trp53<tm1Sia>/Trp53<tm1Sia>	involves: C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Dph1<tm2Bhr>/Dph1<tm2Bhr>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Dph1<tm2Bhr>/Dph1<tm2Bhr>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv * C57BL/6	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:98834	Trp53	"Bard1<tm1Thl>/Bard1<tm1Thl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003204	decreased neuron apoptosis	CCO:MP0003204
MGI:98834	Trp53	"Bard1<tm1Thl>/Bard1<tm1Thl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<+>	involves: 129S7/SvEvBrd * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Bard1<tm1Thl>/Bard1<tm1Thl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Cdc7<tm1Hmas>/Cdc7<tm1Hmas>,Trp53<tm1.1Mok>/Trp53<tm1.1Mok>"	involves: 129S/SvEv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:98834	Trp53	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tsg101<tm1Mak>/Tsg101<tm1Mak>"	involves: 129P3/J * C57BL/6 * CD-1	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:98834	Trp53	"Rb1<tm2Brn>/Rb1<tm2Brn>,Trp53<tm1Brd>/Trp53<+>,Tg(Rbp3-cre)1Brn/0"	involves: 129S7/SvEvBrd * C57BL/6 * FVB/N	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Bard1<tm1Thl>/Bard1<tm1Thl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S1/Sv	MP:0000929	open neural tube	CCO:MP0000929
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0004028	chromosome breakage	CCO:MP0004028
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0002815	adenoma	CCO:MP0002815
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0000343	altered response to myocardial infarction	CCO:MP0000343
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm2Glo>/Trp53<tm2Glo>	involves: 129/Sv * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm2Glo>/Trp53<tm2Glo>	involves: 129/Sv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm2Glo>/Trp53<tm2Glo>	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm2Glo>/Trp53<tm2Glo>	involves: 129/Sv * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:98834	Trp53	Trp53<tm2Glo>/Trp53<tm2Glo>	involves: 129/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129/Sv * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129/Sv * C57BL/6	MP:0002815	adenoma	CCO:MP0002815
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129/Sv * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129/Sv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129/Sv * C57BL/6	MP:0002026	leukemia	CCO:MP0002026
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129/Sv * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv * C57BL/6	MP:0002815	adenoma	CCO:MP0002815
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002815	adenoma	CCO:MP0002815
MGI:98834	Trp53	"Thbs1<tm1Hyn>/Thbs1<tm1Hyn>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Terf1<tm1Tdl>/Terf1<tm1Tdl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129/Sv	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0006043	decreased apoptosis	CCO:MP0006043
MGI:98834	Trp53	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002166	altered tumor susceptibility	CCO:MP0002166
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:98834	Trp53	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:98834	Trp53	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Brca2<tm1Arge>/Brca2<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0000914	exencephaly	CCO:MP0000914
MGI:98834	Trp53	"Brca2<tm1Arge>/Brca2<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Brca2<tm1Arge>/Brca2<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:98834	Trp53	"Brca1<tm1Arge>/Brca1<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0003984	embryonic growth retardation	CCO:MP0003984
MGI:98834	Trp53	Trp53<tm1Brd>/Trp53<tm1Brd>	involves: 129S7/SvEvBrd	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	"Rag2<tm1Fwa>/Rag2<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6 * MF1	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Brca1<tm1Arge>/Brca1<tm1Arge>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S/SvEv * 129S2/SvPas * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Trp53<tm1Brd>/Trp53<tm1Brd>,Wrn<tm1Led>/Wrn<tm1Led>"	either: (involves: 129S/SvEv) or (involves: 129S/SvEv * NIH Black Swiss)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Mdm2<tm1Bay>/Mdm2<tm1Bay>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:98834	Trp53	Trp53<tm1Xu>/Trp53<tm1Xu>	involves: 129S4/SvJae	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:98834	Trp53	"Mdm2<tm1Bay>/Mdm2<tm1Bay>,Trp53<tm1Snj>/Trp53<tm1Snj>"	involves: C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	Trp53<tm1Snj>/Trp53<tm1Snj>	involves: C57BL/6	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:98834	Trp53	"Prkdc<scid>/Prkdc<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6J	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Rad50<tm2Jpt>/Rad50<tm2Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6	MP:0001146	abnormal testis morphology	CCO:MP0001146
MGI:98834	Trp53	"Rag2<tm1Fwa>/Rag2<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6 * MF1	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"H2afx<tm1Fwa>/H2afx<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	"Rag2<tm1Fwa>/Rag2<tm1Fwa>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6 * MF1	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Rag2<tm1Fwa>/Rag2<tm1Fwa>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6 * MF1	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"H2afx<tm1Fwa>/H2afx<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	"H2afx<tm1Fwa>/H2afx<tm1Fwa>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * C57BL/6	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	Trp53<tm1Snj>/Trp53<tm1Snj>	involves: C57BL/6	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:98834	Trp53	"Terf1<tm1Tdl>/Terf1<tm1Tdl>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	129/Sv	MP:0002582	disorganized extraembryonic tissue	CCO:MP0002582
MGI:98834	Trp53	"Prkdc<scid>/Prkdc<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003269	colonic polyps	CCO:MP0003269
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006381	hamartoma	CCO:MP0006381
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003299	gastric polyps	CCO:MP0003299
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Gev>/Trp53<tm1Gev>	involves: 129 * C57BL/6	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002035	leiomyosarcoma	CCO:MP0002035
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Motp1<CE/J>/Motp1<CE/J>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129-Trp53<tm1Tyj>/J * CE/J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nbn<tm1Jpt>/Nbn<tm1Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nbn<tm1Jpt>/Nbn<tm1Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Nbn<tm1Jpt>/Nbn<tm1Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002627	teratoma	CCO:MP0002627
MGI:98834	Trp53	"Nbn<tm1Jpt>/Nbn<tm1Jpt>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Gev>/Trp53<tm1Gev>	involves: 129 * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	Trp53<tm1Adv>/Trp53<tm1Adv>	involves: 129S4/SvJae * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:98834	Trp53	Trp53<tm1Adv>/Trp53<tm1Adv>	involves: 129S4/SvJae * C57BL/6	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	Trp53<tm1Adv>/Trp53<tm1Adv>	involves: 129S4/SvJae * C57BL/6	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	Trp53<tm1Adv>/Trp53<+>	involves: 129S4/SvJae * C57BL/6	MP:0002051	skin papilloma	CCO:MP0002051
MGI:98834	Trp53	Trp53<tm1Adv>/Trp53<+>	involves: 129S4/SvJae * C57BL/6	MP:0005276	skin tumor	CCO:MP0005276
MGI:98834	Trp53	Trp53<tm1Adv>/Trp53<+>	involves: 129S4/SvJae * C57BL/6	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	"Psmb9<tm1Stl>/Psmb9<tm1Stl>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Psmb9<tm1Stl>/Psmb9<tm1Stl>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Psmb9<tm1Stl>/Psmb9<tm1Stl>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129P2/OlaHsd * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0001270	distended abdomen	CCO:MP0001270
MGI:98834	Trp53	"Rb1<tm1Tyj>/Rb1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0009153	pancreas tumor	CCO:MP0009153
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<+>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0001525	impaired balance	CCO:MP0001525
MGI:98834	Trp53	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<+>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0000886	abnormal cerebellar granule layer	CCO:MP0000886
MGI:98834	Trp53	"Motp1<CE/J>/Motp1<CE/J>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129-Trp53<tm1Tyj>/J * CE/J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:98834	Trp53	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002037	fibrohistocytoma	CCO:MP0002037
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002035	leiomyosarcoma	CCO:MP0002035
MGI:98834	Trp53	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<tm1Brd>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"H2afx<tm1Nus>/H2afx<tm1Nus>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Bhlha15<tm2(Kras)Skz>/Bhlha15<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:98834	Trp53	"Bhlha15<tm2(Kras)Skz>/Bhlha15<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Bhlha15<tm2(Kras)Skz>/Bhlha15<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: C57BL/6	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: C57BL/6	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Mdm2<tm1Glo>/Mdm2<tm1Glo>,Trp53<tm3.1Glo>/Trp53<+>"	involves: 129S7/SvEvBrd * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	Trp53<tm3.1Glo>/Trp53<+>	B6.129S7-Trp53<tm3.1Glo>	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002033	malignant triton tumors	CCO:MP0002033
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J * C3H * NIH	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<tm1Ioz>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<tm1Ioz>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Mdm4<tm2.1Glo>/Mdm4<tm2.1Glo>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6J	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002034	malignant peripheral nerve sheath tumors	CCO:MP0002034
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J * C3H * NIH	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<tm1Ioz>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0000708	thymus hyperplasia	CCO:MP0000708
MGI:98834	Trp53	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J * C3H * NIH	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0002052	decreased tumor incidence	CCO:MP0002052
MGI:98834	Trp53	"Cdkn1b<tm1Mlf>/Cdkn1b<tm1Mlf>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J * C3H * NIH	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002039	neuroblastoma	CCO:MP0002039
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:98834	Trp53	Trp53<tm1.1Att>/Trp53<+>	Not Specified	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<tm1Ioz>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<tm1Ioz>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0001954	respiratory distress	CCO:MP0001954
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<tm1Ioz>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<tm1Ioz>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	"Dcn<tm1Ioz>/Dcn<tm1Ioz>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129/Sv * Black Swiss * C57BL/6	MP:0000709	enlarged thymus	CCO:MP0000709
MGI:98834	Trp53	"Stk11<tm1.1Mlfr>/Stk11<+>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J	MP:0006381	hamartoma	CCO:MP0006381
MGI:98834	Trp53	"Nf1<tm1Tyj>/Nf1<+>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129/Sv * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0001544	abnormal cardiovascular system physiology	CCO:MP0001544
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<+>	involves: 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm3.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm3.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm3.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm3.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm3.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<bbl>/Trp53<+>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<bhy>/Trp53<+>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0003789	osteosarcoma	CCO:MP0003789
MGI:98834	Trp53	Trp53<bhy>/Trp53<bhy>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<bhy>/Trp53<bhy>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0002026	leukemia	CCO:MP0002026
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	"Prdm2<tm1Shg>/Prdm2<tm1Shg>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Prdm2<tm1Shg>/Prdm2<tm1Shg>,Trp53<tm1Tyj>/Trp53<+>"	involves: 129S2/SvPas * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	Trp53<tm4Tyj>/Trp53<tm4Tyj>	involves: 129S4/SvJae * C57BL/6	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0004025	polyploidy	CCO:MP0004025
MGI:98834	Trp53	Trp53<bbl>/Trp53<+>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	Trp53<bbl>/Trp53<+>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	Trp53<bbl>/Trp53<+>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0002627	teratoma	CCO:MP0002627
MGI:98834	Trp53	Trp53<bbl>/Trp53<+>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Nf1<tm1Tyj>/?,Trp53<tm1Tyj>/?,Mastr<C57BL/6J>/?"	involves: 129S4/SvJae * C57BL/6J	MP:0002018	malignant tumors	CCO:MP0002018
MGI:98834	Trp53	"Nf1<tm1Tyj>/?,Trp53<tm1Tyj>/?,Mastr<129S4/SvJae>/?"	involves: 129S4/SvJae * C57BL/6J	MP:0005514	increased resistance to tumor development	CCO:MP0005514
MGI:98834	Trp53	"Ccne1<tm1Jro>/?,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	either: (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6J) or (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * C57BL/6J)	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Ccne1<tm1Jro>/?,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	either: (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6J) or (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * C57BL/6J)	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0006414	decreased T cell apoptosis	CCO:MP0006414
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0008411	decreased cellular sensitivity to ultraviolet irradiation	CCO:MP0008411
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<bbl>/Trp53<+>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:98834	Trp53	Trp53<bbl>/Trp53<+>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<bbl>/Trp53<bbl>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	Trp53<bbl>/Trp53<bbl>	C57BL/6Apb-Trp53<bbl>/Apb	MP:0002026	leukemia	CCO:MP0002026
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0005601	increased angiogenesis	CCO:MP0005601
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0001625	cardiac hypertrophy	CCO:MP0001625
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm1Tyj>	involves: 129S2/SvPas	MP:0006283	medulloblastoma	CCO:MP0006283
MGI:98834	Trp53	"Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Trp53<tm1Thl>/Trp53<tm1Thl>,Tg(Pbsn-cre)4Prb/0"	involves: 129S1/Sv * C57BL/6 * DBA/2	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	"Tg(MMTV-cre)AElee/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * C57BL/6	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:98834	Trp53	Trp53<bhy>/Trp53<+>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0002029	fibrosarcoma	CCO:MP0002029
MGI:98834	Trp53	"Nbn<tm2Zqw>/Nbn<tm2Zqw>,Trp53<tm1Brd>/Trp53<+>,Tg(Nes-cre)1Wme/0"	involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA	MP:0000857	abnormal cerebellar foliation	CCO:MP0000857
MGI:98834	Trp53	"Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0000350	abnormal cell proliferation	CCO:MP0000350
MGI:98834	Trp53	Trp53<bhy>/Trp53<+>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	Trp53<bhy>/Trp53<+>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0002627	teratoma	CCO:MP0002627
MGI:98834	Trp53	Trp53<bhy>/Trp53<+>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:98834	Trp53	Trp53<bhy>/Trp53<+>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	"Chek1<tm1Sje>/Chek1<tm1Sje>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Trp53<tm1Thl>/Trp53<tm1Thl>,Tg(Pbsn-cre)4Prb/0"	involves: 129S1/Sv * C57BL/6 * DBA/2	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(MMTV-cre)AElee/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * C57BL/6	MP:0002022	lymphoma	CCO:MP0002022
MGI:98834	Trp53	"Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Trp53<tm1Thl>/Trp53<tm1Thl>,Tg(Pbsn-cre)4Prb/0"	involves: 129S1/Sv * C57BL/6 * DBA/2	MP:0003606	kidney failure	CCO:MP0003606
MGI:98834	Trp53	"Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Trp53<tm1Thl>/Trp53<tm1Thl>,Tg(Pbsn-cre)4Prb/0"	involves: 129S1/Sv * C57BL/6 * DBA/2	MP:0003831	prostate tumor	CCO:MP0003831
MGI:98834	Trp53	"Pten<tm2.1Ppp>/Pten<tm2.1Ppp>,Trp53<tm1Thl>/Trp53<tm1Thl>,Tg(Pbsn-cre)4Prb/0"	involves: 129S1/Sv * C57BL/6 * DBA/2	MP:0009552	urinary bladder obstruction	CCO:MP0009552
MGI:98834	Trp53	"Ubr5<tm1Ckww>/Ubr5<tm1Ckww>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129S2/SvPas * 129X1/SvJ * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Npm1<tm1Ppp>/Npm1<tm1Ppp>,Trp53<tm1Brd>/Trp53<+>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	"Npm1<tm1Ppp>/Npm1<tm1Ppp>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0006208	lethality throughout fetal growth and development	CCO:MP0006208
MGI:98834	Trp53	"Npm1<tm1Ppp>/Npm1<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm4Tyj>/Trp53<tm4Tyj>	involves: 129S4/SvJae * C57BL/6	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm4Tyj>/Trp53<tm4Tyj>	involves: 129S4/SvJae * C57BL/6	MP:0002032	sarcoma	CCO:MP0002032
MGI:98834	Trp53	Trp53<tm4Tyj>/Trp53<tm4Tyj>	involves: 129S4/SvJae * C57BL/6	MP:0002023	B cell derived lymphoma	CCO:MP0002023
MGI:98834	Trp53	"Chek1<tm1Sje>/Chek1<tm1Sje>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: 129S7/SvEvBrd	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:98834	Trp53	Trp53<tm2.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0000351	increased cell proliferation	CCO:MP0000351
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm2.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm2.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:98834	Trp53	Trp53<bhy>/Trp53<bhy>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0001914	hemorrhage	CCO:MP0001914
MGI:98834	Trp53	Trp53<bhy>/Trp53<+>	C57BL/6Apb-Trp53<bhy>/Apb	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Tg(Wap-rtTA-cre)10Whl/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm2.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002038	carcinoma	CCO:MP0002038
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm2.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm2.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	Trp53<tm1Tyj>/Trp53<tm2.1Tyj>	involves: 129S2/SvPas * 129S4/SvJae	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	Trp53<tm2.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	"H2afx<tm1Nus>/H2afx<tm1Nus>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:98834	Trp53	Trp53<tm2.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0000067	osteopetrosis	CCO:MP0000067
MGI:98834	Trp53	"Npm1<Gt(VICTR37)704Lex>/Npm1<Gt(VICTR37)704Lex>,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:98834	Trp53	Trp53<tm2.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(Wap-rtTA-cre)10Whl/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * C57BL/6	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Tg(MMTV-cre)BElee/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"Tg(MMTV-cre)BElee/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * C57BL/6	MP:0001883	mammary adenocarcinoma	CCO:MP0001883
MGI:98834	Trp53	"Tg(ACTB-NOTCH1)1Shn/0,Tg(Nes-cre)1Kln/0,Trp53<tm1Tyj>/Trp53<tm1Tyj>"	involves: C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:98834	Trp53	"Tg(ACTB-NOTCH1)1Shn/0,Tg(Nes-cre)1Kln/0,Trp53<tm1Tyj>/Trp53<+>"	involves: C57BL/6J	MP:0001648	abnormal apoptosis	CCO:MP0001648
MGI:98834	Trp53	"H2afx<tm1Nus>/H2afx<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J	MP:0002021	increased incidence of induced tumors	CCO:MP0002021
MGI:98834	Trp53	"Tg(MMTV-cre)AElee/0,Trp53<tm1Elee>/Trp53<+>"	involves: 129S4/SvJae * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:98834	Trp53	"H2afx<tm1Nus>/H2afx<+>,Trp53<tm1Brd>/Trp53<tm1Brd>"	involves: C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:98834	Trp53	"Tg(MMTV-cre)AElee/0,Trp53<tm1Elee>/Trp53<tm1Elee>"	involves: 129S4/SvJae * C57BL/6	MP:0006318	mammary gland tumor	CCO:MP0006318
MGI:98834	Trp53	Trp53<tm3.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0003207	decreased cellular sensitivity to gamma-irradiation	CCO:MP0003207
MGI:98834	Trp53	Trp53<tm2.1Tyj>/Trp53<+>	involves: 129S4/SvJae	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<tm1Xlu>	involves: C57BL/6J	MP:0000440	domed skull	CCO:MP0000440
MGI:2138319	Trp53bp2	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Trp53bp2<tm1Xlu>/Trp53bp2<tm1Xlu>"	involves: 129S2/SvPas * C57BL/6J	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:2138319	Trp53bp2	"Trp53<tm1Tyj>/Trp53<+>,Trp53bp2<tm1Xlu>/Trp53bp2<tm1Xlu>"	involves: 129S2/SvPas * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:2138319	Trp53bp2	"Trp53<tm1Tyj>/Trp53<+>,Trp53bp2<tm1Xlu>/Trp53bp2<+>"	involves: 129S2/SvPas * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<tm1Xlu>	involves: C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<+>	involves: C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<+>	involves: C57BL/6J	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<+>	involves: C57BL/6J	MP:0002036	rhabdomyosarcoma	CCO:MP0002036
MGI:2138319	Trp53bp2	"Trp53<tm1Tyj>/Trp53<+>,Trp53bp2<tm1Xlu>/Trp53bp2<+>"	involves: 129S2/SvPas * C57BL/6J	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<tm1Xlu>	involves: C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<tm1Xlu>	involves: C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<+>	involves: C57BL/6J	MP:0002007	increased cellular sensitivity to gamma-irradiation	CCO:MP0002007
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<+>	involves: C57BL/6J	MP:0002025	B cell/T cell derived lymphoma	CCO:MP0002025
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<+>	involves: C57BL/6J	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:2138319	Trp53bp2	Trp53bp2<tm1Xlu>/Trp53bp2<+>	involves: C57BL/6J	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:2138319	Trp53bp2	Trp53bp2<tm1Cdlo>/Trp53bp2<+>	involves: 129X1/SvJ * C57BL/6	MP:0002444	abnormal T cell physiology	CCO:MP0002444
MGI:2138319	Trp53bp2	"Trp53bp2<tm1Cdlo>/Trp53bp2<+>,Tg(EmuSR-tTa)83Bop/0,Tg(tetO-MYC)36Bop/0"	involves: 129X1/SvJ * C57BL/6 * FVB/N	MP:0002024	T cell derived lymphoma	CCO:MP0002024
MGI:2138319	Trp53bp2	"Trp53<tm1Brd>/Trp53<+>,Trp53bp2<tm1Cdlo>/Trp53bp2<+>"	involves: 129S7/SvEvBrd * 129X1/SvJ * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2138319	Trp53bp2	Trp53bp2<tm1Cdlo>/Trp53bp2<+>	involves: 129X1/SvJ * C57BL/6	MP:0004045	abnormal cell cycle checkpoint function	CCO:MP0004045
MGI:2138319	Trp53bp2	Trp53bp2<tm1Cdlo>/Trp53bp2<+>	involves: 129X1/SvJ * C57BL/6	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:2138319	Trp53bp2	Trp53bp2<tm1Cdlo>/Trp53bp2<tm1Cdlo>	involves: 129X1/SvJ * C57BL/6	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:2138319	Trp53bp2	Trp53bp2<tm1Cdlo>/Trp53bp2<+>	involves: 129X1/SvJ * C57BL/6	MP:0004500	increased incidence of ionizing radiation-induced tumors	CCO:MP0004500
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0000511	abnormal intestinal mucosa morphology	CCO:MP0000511
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0002044	colonic adenoma	CCO:MP0002044
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0003304	large intestinal inflammation	CCO:MP0003304
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0008537	increased susceptibility to induced colitis	CCO:MP0008537
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0000490	abnormal crypts of Lieberkuhn morphology	CCO:MP0000490
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0003674	oxidative stress	CCO:MP0003674
MGI:1926609	Trp53inp1	Trp53inp1<tm1Acar>/Trp53inp1<tm1Acar>	involves: 129/Sv * C57BL/6	MP:0005455	increased weight gain	CCO:MP0005455
MGI:1330810	Trp63	Trp63<tm2Fmc>/Trp63<tm2Fmc>	involves: BALB/c	MP:0004228	decreased cellular sensitivity to ionizing radiation	CCO:MP0004228
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<+>	involves: 129S4/SvJae	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<+>	involves: 129S4/SvJae	MP:0002637	small uterus	CCO:MP0002637
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0009228	cervix inflammation	CCO:MP0009228
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0001859	kidney inflammation	CCO:MP0001859
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0001394	circling	CCO:MP0001394
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0000492	abnormal rectum morphology	CCO:MP0000492
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0002083	premature death	CCO:MP0002083
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0000702	enlarged lymph nodes	CCO:MP0000702
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0002406	increased susceptibility to infection	CCO:MP0002406
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0000764	abnormal tongue epithelium morphology	CCO:MP0000764
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0000746	weakness	CCO:MP0000746
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0006000	abnormal corneal epithelium morphology	CCO:MP0006000
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0000414	alopecia	CCO:MP0000414
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0001212	skin lesions	CCO:MP0001212
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0001209	spontaneous skin ulceration	CCO:MP0001209
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0001874	acanthosis	CCO:MP0001874
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0000493	rectal prolapse	CCO:MP0000493
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0003786	premature aging	CCO:MP0003786
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0001137	abnormal cervical epithelium	CCO:MP0001137
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1330810	Trp63	"Trp63<tm1Aam>/Trp63<tm1Aam>,Dlx5<tm1Levi>/Dlx5/Dlx6<tm1Levi>"	involves: 129P2/OlaHsd	MP:0000564	syndactyly	CCO:MP0000564
MGI:1330810	Trp63	"Dlx5<tm1Levi>/Dlx5/Dlx6<tm1Levi>,Trp63<tm1Aam>/Trp63<tm1Aam>"	involves: 129P2/OlaHsd	MP:0003800	monodactyly	CCO:MP0003800
MGI:1330810	Trp63	"Dlx5<tm1Levi>/Dlx5/Dlx6<tm1Levi>,Trp63<tm1Aam>/Trp63<tm1Aam>"	involves: 129P2/OlaHsd	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:1330810	Trp63	"Dlx5<tm1Levi>/Dlx5/Dlx6<tm1Levi>,Trp63<tm1Aam>/Trp63<tm1Aam>"	involves: 129P2/OlaHsd	MP:0005230	ectrodactyly	CCO:MP0005230
MGI:1330810	Trp63	"Dlx5<tm1Levi>/Dlx5/Dlx6<tm1Levi>,Trp63<tm1Aam>/Trp63<tm1Aam>"	involves: 129P2/OlaHsd	MP:0000564	syndactyly	CCO:MP0000564
MGI:1330810	Trp63	Trp63<tm1Aam>/Trp63<+>	Not Specified	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:1330810	Trp63	"Trp63<tm1Aam>/Trp63<tm1Aam>,Dlx5<tm1Levi>/Dlx5/Dlx6<tm1Levi>"	involves: 129P2/OlaHsd	MP:0005230	ectrodactyly	CCO:MP0005230
MGI:1330810	Trp63	Trp63<tm1Aam>/Trp63<tm1Aam>	Not Specified	MP:0000557	absent hindlimb	CCO:MP0000557
MGI:1330810	Trp63	Trp63<tm1Aam>/Trp63<+>	Not Specified	MP:0005230	ectrodactyly	CCO:MP0005230
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:1330810	Trp63	Trp63<tm1Aam>/Trp63<tm1Aam>	Not Specified	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:1330810	Trp63	Trp63<tm1Aam>/Trp63<tm1Aam>	Not Specified	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:1330810	Trp63	Trp63<tm1Aam>/Trp63<tm1Aam>	Not Specified	MP:0001675	abnormal ectoderm development	CCO:MP0001675
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<+>	involves: 129S7/SvEvBrd	MP:0001270	distended abdomen	CCO:MP0001270
MGI:1330810	Trp63	Trp63<tm3.2Brd>/Trp63<tm3.2Brd>	involves: 129S7/SvEvBrd	MP:0000557	absent hindlimb	CCO:MP0000557
MGI:1330810	Trp63	Trp63<tm1Aam>/Trp63<tm1Aam>	Not Specified	MP:0004575	small limb buds	CCO:MP0004575
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd	MP:0001676	abnormal apical ectodermal ridge	CCO:MP0001676
MGI:1330810	Trp63	"Tg(KRT5-cre/PGR)1Der/0,Trp63<tm2Brd>/Trp63<tm3.1Brd>"	involves: 129S7/SvEvBrd * FVB * ICR	MP:0000414	alopecia	CCO:MP0000414
MGI:1330810	Trp63	"Tg(KRT5-cre/PGR)1Der/0,Trp63<tm2Brd>/Trp63<tm3.1Brd>"	involves: 129S7/SvEvBrd * FVB * ICR	MP:0000160	kyphosis	CCO:MP0000160
MGI:1330810	Trp63	"Tg(KRT5-cre/PGR)1Der/0,Trp63<tm2Brd>/Trp63<tm3.1Brd>"	involves: 129S7/SvEvBrd * FVB * ICR	MP:0001263	weight loss	CCO:MP0001263
MGI:1330810	Trp63	"Tg(KRT5-cre/PGR)1Der/0,Trp63<tm2Brd>/Trp63<tm3.1Brd>"	involves: 129S7/SvEvBrd * FVB * ICR	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:1330810	Trp63	"Tg(KRT5-cre/PGR)1Der/0,Trp63<tm2Brd>/Trp63<tm3.1Brd>"	involves: 129S7/SvEvBrd * FVB * ICR	MP:0002060	abnormal skin morphology	CCO:MP0002060
MGI:1330810	Trp63	Trp63<tm1Aam>/Trp63<tm1Aam>	Not Specified	MP:0001676	abnormal apical ectodermal ridge	CCO:MP0001676
MGI:1330810	Trp63	"Trp63<tm1Aam>/Trp63<tm1Aam>,Dlx5<tm1Levi>/Dlx5/Dlx6<tm1Levi>"	involves: 129P2/OlaHsd	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:1330810	Trp63	"Tg(KRT5-cre/PGR)1Der/0,Trp63<tm2Brd>/Trp63<tm3.1Brd>"	involves: 129S7/SvEvBrd * FVB * ICR	MP:0002109	abnormal limb morphology	CCO:MP0002109
MGI:1330810	Trp63	"Tg(KRT5-cre/PGR)1Der/0,Trp63<tm2Brd>/Trp63<tm3.1Brd>"	involves: 129S7/SvEvBrd * FVB * ICR	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:1330810	Trp63	"Tg(KRT5-cre/PGR)1Der/0,Trp63<tm2Brd>/Trp63<tm3.1Brd>"	involves: 129S7/SvEvBrd * FVB * ICR	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:1330810	Trp63	Trp63<tm3.1Brd>/Trp63<tm3.1Brd>	involves: 129S7/SvEvBrd	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:1330810	Trp63	Trp63<tm3.1Brd>/Trp63<tm3.1Brd>	involves: 129S7/SvEvBrd	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:1330810	Trp63	Trp63<tm3.2Brd>/Trp63<tm3.2Brd>	involves: 129S7/SvEvBrd	MP:0000378	absent hair follicles	CCO:MP0000378
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd	MP:0008008	early cellular replicative senescence	CCO:MP0008008
MGI:1330810	Trp63	Trp63<tm3.2Brd>/Trp63<tm3.2Brd>	involves: 129S7/SvEvBrd	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:1330810	Trp63	Trp63<tm3Brd>/Trp63<tm3Brd>	involves: 129S7/SvEvBrd	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1330810	Trp63	"Trp63<tm1Aam>/Trp63<tm1Aam>,Dlx5<tm1Levi>/Dlx5/Dlx6<tm1Levi>"	involves: 129P2/OlaHsd	MP:0003800	monodactyly	CCO:MP0003800
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0003578	absent ovary	CCO:MP0003578
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0003125	abnormal septation of the cloaca	CCO:MP0003125
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000549	absent limbs	CCO:MP0000549
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0001217	absent epidermis	CCO:MP0001217
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0001341	absent eyelids	CCO:MP0001341
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000117	absent tooth primordium	CCO:MP0000117
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000378	absent hair follicles	CCO:MP0000378
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000469	abnormal esophageal squamous epithelium morphology	CCO:MP0000469
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000472	abnormal stomach squamous epithelium morphology	CCO:MP0000472
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0001140	abnormal vagina epithelium morphology	CCO:MP0001140
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0001677	absent apical ectodermal ridge	CCO:MP0001677
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000468	abnormal esophageal epithelium morphology	CCO:MP0000468
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0002861	abnormal tail bud morphology	CCO:MP0002861
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0001137	abnormal cervical epithelium	CCO:MP0001137
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0003384	abnormal ventral body wall	CCO:MP0003384
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0003575	absent oviduct	CCO:MP0003575
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0003755	abnormal palate morphology	CCO:MP0003755
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0003809	abnormal hair shaft morphology	CCO:MP0003809
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0006279	abnormal limb development	CCO:MP0006279
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0004540	small maxilla	CCO:MP0004540
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0004592	small mandible	CCO:MP0004592
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0009101	clitoris hypoplasia	CCO:MP0009101
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0003320	rectovaginal fistula	CCO:MP0003320
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000766	absent tongue squamous epithelium	CCO:MP0000766
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000629	absent mammary gland	CCO:MP0000629
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000541	abnormal urinary bladder transitional epithelium morphology	CCO:MP0000541
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0001347	absent lacrimal glands	CCO:MP0001347
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000614	absent salivary gland	CCO:MP0000614
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000648	absent sebaceous gland	CCO:MP0000648
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0001119	abnormal female reproductive system morphology	CCO:MP0001119
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0001284	absent vibrissae	CCO:MP0001284
MGI:1330810	Trp63	Trp63<tm1Fmc>/Trp63<tm1Fmc>	involves: 129S4/SvJae	MP:0000428	abnormal craniofacial morphology	CCO:MP0000428
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0009614	absent epidermis stratum spinosum	CCO:MP0009614
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0009560	absent epidermis stratum granulosum	CCO:MP0009560
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0004575	small limb buds	CCO:MP0004575
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0004509	abnormal pelvic girdle bone morphology	CCO:MP0004509
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0004360	absent ulna	CCO:MP0004360
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003743	abnormal facial morphology	CCO:MP0003743
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003704	abnormal hair follicle development	CCO:MP0003704
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000555	absent carpal bone	CCO:MP0000555
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002796	impaired skin barrier function	CCO:MP0002796
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005296	abnormal humerus morphology	CCO:MP0005296
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001677	absent apical ectodermal ridge	CCO:MP0001677
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001241	absent epidermis stratum corneum	CCO:MP0001241
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000557	absent hindlimb	CCO:MP0000557
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000124	absent teeth	CCO:MP0000124
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001196	shiny skin	CCO:MP0001196
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000553	absent radius	CCO:MP0000553
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005501	abnormal skin physiology	CCO:MP0005501
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001677	absent apical ectodermal ridge	CCO:MP0001677
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0009560	absent epidermis stratum granulosum	CCO:MP0009560
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0004509	abnormal pelvic girdle bone morphology	CCO:MP0004509
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0004360	absent ulna	CCO:MP0004360
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003743	abnormal facial morphology	CCO:MP0003743
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0003704	abnormal hair follicle development	CCO:MP0003704
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005501	abnormal skin physiology	CCO:MP0005501
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002796	impaired skin barrier function	CCO:MP0002796
MGI:1330810	Trp63	Trp63<tm1Brd>/Trp63<tm1Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001201	translucent skin	CCO:MP0001201
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005296	abnormal humerus morphology	CCO:MP0005296
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0009614	absent epidermis stratum spinosum	CCO:MP0009614
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001241	absent epidermis stratum corneum	CCO:MP0001241
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000557	absent hindlimb	CCO:MP0000557
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000124	absent teeth	CCO:MP0000124
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000553	absent radius	CCO:MP0000553
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000555	absent carpal bone	CCO:MP0000555
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002058	neonatal lethality	CCO:MP0002058
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001201	translucent skin	CCO:MP0001201
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001196	shiny skin	CCO:MP0001196
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0000550	abnormal forelimb morphology	CCO:MP0000550
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001191	abnormal skin condition	CCO:MP0001191
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0001216	abnormal epidermal layer morphology	CCO:MP0001216
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0002115	abnormal skeleton extremities morphology	CCO:MP0002115
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0005306	abnormal phalanx morphology	CCO:MP0005306
MGI:1330810	Trp63	Trp63<tm2Brd>/Trp63<tm2Brd>	involves: 129S7/SvEvBrd * C57BL/6J	MP:0004575	small limb buds	CCO:MP0004575
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0008869	anovulation	CCO:MP0008869
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003718	maternal effect	CCO:MP0003718
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005431	decreased oocyte cell number	CCO:MP0005431
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004023	abnormal chromosome number	CCO:MP0004023
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001926	female infertility	CCO:MP0001926
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004499	increased incidence of chemically-induced tumors	CCO:MP0004499
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0008871	abnormal ovarian follicle number	CCO:MP0008871
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002038	carcinoma	CCO:MP0002038
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001928	abnormal ovulation	CCO:MP0001928
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0004025	polyploidy	CCO:MP0004025
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005234	thymic lymphoma	CCO:MP0005234
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000807	abnormal hippocampus morphology	CCO:MP0000807
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0005168	abnormal female meiosis	CCO:MP0005168
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<tm1Mak>	involves: 129P2/OlaHsd * C57BL/6J	MP:0000812	abnormal dentate gyrus morphology	CCO:MP0000812
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0003667	hemangiosarcoma	CCO:MP0003667
MGI:1336991	Trp73	Trp73<tm1Mak>/Trp73<+>	involves: 129P2/OlaHsd * C57BL/6J	MP:0002022	lymphoma	CCO:MP0002022
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0000465	gastrointestinal hemorrhage	CCO:MP0000465
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001893	non-obstructive hydrocephaly	CCO:MP0001893
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001852	conjunctivitis	CCO:MP0001852
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0002243	abnormal vomeronasal organ morphology	CCO:MP0002243
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001850	increased susceptibility to otitis media	CCO:MP0001850
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001926	female infertility	CCO:MP0001926
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001891	hydroencephaly	CCO:MP0001891
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001917	intraventricular hemorrhage	CCO:MP0001917
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001265	decreased body size	CCO:MP0001265
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001911	abnormal cerebrospinal fluid production	CCO:MP0001911
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001355	submission towards male mice	CCO:MP0001355
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001380	male reduced copulation	CCO:MP0001380
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0002499	chronic inflammation	CCO:MP0002499
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001867	rhinitis	CCO:MP0001867
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0000344	absent Cajal-Retzius cell	CCO:MP0000344
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0000440	domed skull	CCO:MP0000440
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001788	periorbital edema	CCO:MP0001788
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0002412	increased susceptibility to bacterial infection	CCO:MP0002412
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0009485	distended ileum	CCO:MP0009485
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0000825	dilated lateral ventricles	CCO:MP0000825
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0000812	abnormal dentate gyrus morphology	CCO:MP0000812
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0000808	abnormal hippocampus development	CCO:MP0000808
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0005150	cachexia	CCO:MP0005150
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001915	intracranial hemorrhage	CCO:MP0001915
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0000504	excessive digestive mucosecretion	CCO:MP0000504
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0005442	abnormal pyramidal neuron morphology	CCO:MP0005442
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0001872	sinus inflammation	CCO:MP0001872
MGI:1336991	Trp73	Trp73<tm1Fmc>/Trp73<tm1Fmc>	involves: 129S4/SvJae	MP:0000487	absent enterocytes	CCO:MP0000487
MGI:2153272	Trrap	Trrap<tm1Zqw>/Trrap<tm1Zqw>	involves: 129P2/OlaHsd	MP:0008762	embryonic lethality	CCO:MP0008762
MGI:2153272	Trrap	Trrap<tm1.1Zqw>/Trrap<tm1.1Zqw>	involves: 129P2/OlaHsd	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:2153272	Trrap	Trrap<tm1.1Zqw>/Trrap<tm1.1Zqw>	involves: 129P2/OlaHsd	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:2153272	Trrap	Trrap<tm1.1Zqw>/Trrap<tm1.1Zqw>	involves: 129P2/OlaHsd	MP:0005033	abnormal trophoblast giant cells	CCO:MP0005033
MGI:2153272	Trrap	Trrap<tm1.1Zqw>/Trrap<tm1.1Zqw>	involves: 129P2/OlaHsd	MP:0002086	abnormal extraembryonic tissue morphology	CCO:MP0002086
MGI:2153272	Trrap	Trrap<tm1.1Zqw>/Trrap<tm1.1Zqw>	involves: 129P2/OlaHsd	MP:0005031	abnormal trophoblast layer morphology	CCO:MP0005031
MGI:2153272	Trrap	Trrap<tm1.1Zqw>/Trrap<tm1.1Zqw>	involves: 129P2/OlaHsd	MP:0004964	absent inner cell mass	CCO:MP0004964
MGI:106581	Tsg101	"Tsg101<tm1Kuw>/Tsg101<tm1Kuw>,Tg(Wap-cre)11738Mam/0"	involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL	MP:0006270	abnormal mammary gland growth during lactation	CCO:MP0006270
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001695	abnormal gastrulation	CCO:MP0001695
MGI:106581	Tsg101	Tsg101<tm1.1Kuw>/Tsg101<tm1.1Kuw>	Not Specified	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:106581	Tsg101	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tsg101<tm1Mak>/Tsg101<tm1Mak>"	involves: 129P3/J * C57BL/6 * CD-1	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:106581	Tsg101	Tsg101<tm1Kuw>/Tsg101<tm1Kuw>	Not Specified	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:106581	Tsg101	"Tsg101<tm1Kuw>/Tsg101<tm1Kuw>,Tg(Wap-cre)11738Mam/0"	Not Specified	MP:0006270	abnormal mammary gland growth during lactation	CCO:MP0006270
MGI:106581	Tsg101	"Tsg101<tm1Kuw>/Tsg101<tm1Kuw>,Tg(Wap-cre)11738Mam/0"	Not Specified	MP:0001882	abnormal lactation	CCO:MP0001882
MGI:106581	Tsg101	"Tsg101<tm1Kuw>/Tsg101<tm1Kuw>,Tg(Wap-cre)11738Mam/0"	Not Specified	MP:0000628	abnormal mammary gland development	CCO:MP0000628
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0000352	decreased cell proliferation	CCO:MP0000352
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0002582	disorganized extraembryonic tissue	CCO:MP0002582
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001685	abnormal endoderm development	CCO:MP0001685
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0004759	decreased mitotic index	CCO:MP0004759
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:106581	Tsg101	"Trp53<tm1Tyj>/Trp53<tm1Tyj>,Tsg101<tm1Mak>/Tsg101<tm1Mak>"	involves: 129P3/J * C57BL/6 * CD-1	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0004966	abnormal inner cell mass proliferation	CCO:MP0004966
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0003890	abnormal embryonic-extraembryonic boundary morphology	CCO:MP0003890
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001724	abnormal extraembryonic endoderm formation	CCO:MP0001724
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0006206	embryonic lethality before turning of embryo	CCO:MP0006206
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001693	failure of primitive streak formation	CCO:MP0001693
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:106581	Tsg101	Tsg101<tm1Mak>/Tsg101<tm1Mak>	either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1)	MP:0001683	absent mesoderm	CCO:MP0001683
MGI:107814	Tubb1	Tubb1<tm1Shiv>/Tubb1<tm1Shiv>	Not Specified	MP:0003405	abnormal platelet shape	CCO:MP0003405
MGI:107814	Tubb1	Tubb1<tm1Shiv>/Tubb1<tm1Shiv>	Not Specified	MP:0005464	abnormal platelet physiology	CCO:MP0005464
MGI:107814	Tubb1	Tubb1<tm1Shiv>/Tubb1<tm1Shiv>	involves: 129/Sv * BALB/c	MP:0003405	abnormal platelet shape	CCO:MP0003405
MGI:107814	Tubb1	Tubb1<tm1Shiv>/Tubb1<tm1Shiv>	involves: 129/Sv * BALB/c	MP:0003179	decreased platelet cell number	CCO:MP0003179
MGI:107814	Tubb1	Tubb1<tm1Shiv>/Tubb1<tm1Shiv>	involves: 129/Sv * BALB/c	MP:0005606	increased bleeding time	CCO:MP0005606
MGI:101834	Tubg1	Tubg1<tm1Sts>/Tubg1<tm1Sts>	involves: 129S4/SvJae * C57BL/6J	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:101834	Tubg1	Tubg1<tm1Sts>/Tubg1<tm1Sts>	involves: 129S4/SvJae * C57BL/6J	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<Hyplip1>	HcB19/Dem-Txnip<Hyplip1>	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<Hyplip1>	HcB19/Dem-Txnip<Hyplip1>	MP:0001552	increased circulating triglyceride level	CCO:MP0001552
MGI:1889549	Txnip	Txnip<Gt(ROSA)83Sor>/Txnip<Gt(ROSA)83Sor>	involves: 129S4/SvJaeSor	MP:0002169	no abnormal phenotype detected	CCO:MP0002169
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<Hyplip1>	HcB19/Dem-Txnip<Hyplip1>	MP:0005178	increased circulating cholesterol level	CCO:MP0005178
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<+>	involves: CAST/Ei * HcB19/Dem	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<Hyplip1>	involves: CAST/Ei * HcB19/Dem	MP:0003331	hepatocellular carcinoma	CCO:MP0003331
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<Hyplip1>	B6.HcB19-Txnip<Hyplip1>	MP:0002118	abnormal lipid homeostasis	CCO:MP0002118
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<Hyplip1>	B6.HcB19-Txnip<Hyplip1>	MP:0005281	increased fatty acid level	CCO:MP0005281
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<Hyplip1>	B6.HcB19-Txnip<Hyplip1>	MP:0002981	increased liver weight	CCO:MP0002981
MGI:1889549	Txnip	Txnip<Hyplip1>/Txnip<Hyplip1>	HcB19/Dem-Txnip<Hyplip1>	MP:0005145	increased circulating VLDL cholesterol level	CCO:MP0005145
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0004130	abnormal muscle cell glucose uptake	CCO:MP0004130
MGI:1889549	Txnip	"Txnip<tm1Rlee>/Txnip<tm1Rlee>,Tg(Myh6-cre/Esr1)1Jmk/0"	involves: 129S4/SvJae * FVB	MP:0004484	altered response of heart to induced stress	CCO:MP0004484
MGI:1889549	Txnip	Txnip<tm1.1Rlee>/Txnip<tm1.1Rlee>	involves: 129S4/SvJae	MP:0004484	altered response of heart to induced stress	CCO:MP0004484
MGI:1889549	Txnip	Txnip<tm1.1Rlee>/Txnip<tm1.1Rlee>	involves: 129S4/SvJae	MP:0004039	abnormal cardiac cell glucose uptake	CCO:MP0004039
MGI:1889549	Txnip	Txnip<tm1.1Rlee>/Txnip<tm1.1Rlee>	involves: 129S4/SvJae	MP:0003921	abnormal heart left ventricle morphology	CCO:MP0003921
MGI:1889549	Txnip	Txnip<tm1.1Rlee>/Txnip<tm1.1Rlee>	involves: 129S4/SvJae	MP:0005598	decreased ventricle muscle contractility	CCO:MP0005598
MGI:1889549	Txnip	Txnip<tm1.1Rlee>/Txnip<tm1.1Rlee>	involves: 129S4/SvJae	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:1889549	Txnip	"Txnip<tm1Rlee>/Txnip<tm1Rlee>,Tg(Myh6-cre/Esr1)1Jmk/0"	involves: 129S4/SvJae * FVB	MP:0004039	abnormal cardiac cell glucose uptake	CCO:MP0004039
MGI:1889549	Txnip	"Txnip<tm1Road>/Txnip<tm1Road>,Tg(Ckmm-cre)5Khn/0"	involves: C57BL/6 * FVB	MP:0002575	increased circulating ketone body level	CCO:MP0002575
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0006041	decreased mitochondrial oxidation	CCO:MP0006041
MGI:1889549	Txnip	"Txnip<tm1Road>/Txnip<tm1Road>,Tg(Ckmm-cre)5Khn/0"	involves: C57BL/6 * FVB	MP:0001552	increased circulating triglyceride level	CCO:MP0001552
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0002078	abnormal glucose homeostasis	CCO:MP0002078
MGI:1889549	Txnip	"Txnip<tm1Road>/Txnip<tm1Road>,Tg(Ckmm-cre)5Khn/0"	involves: C57BL/6 * FVB	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0008874	decreased sensitivity to xenobiotics	CCO:MP0008874
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0003383	abnormal gluconeogenesis	CCO:MP0003383
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0002891	increased insulin sensitivity	CCO:MP0002891
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0005292	improved glucose tolerance	CCO:MP0005292
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0001552	increased circulating triglyceride level	CCO:MP0001552
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0002575	increased circulating ketone body level	CCO:MP0002575
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0000189	hypoglycemia	CCO:MP0000189
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0000179	abnormal blood chemistry	CCO:MP0000179
MGI:1889549	Txnip	Txnip<tm1.1Road>/Txnip<tm1.1Road>	B6.Cg-Txnip<tm1.1Road>	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:1889549	Txnip	"Txnip<tm1Road>/Txnip<tm1Road>,Tg(Ckmm-cre)5Khn/0"	involves: C57BL/6 * FVB	MP:0005292	improved glucose tolerance	CCO:MP0005292
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0003103	liver degeneration	CCO:MP0003103
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0005627	increased circulating potassium level	CCO:MP0005627
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0005565	increased blood urea nitrogen level	CCO:MP0005565
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0005560	decreased circulating glucose level	CCO:MP0005560
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0005178	increased circulating cholesterol level	CCO:MP0005178
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0005161	hematuria	CCO:MP0005161
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0006084	abnormal circulating phospholipid level	CCO:MP0006084
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0002078	abnormal glucose homeostasis	CCO:MP0002078
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0005634	decreased circulating sodium level	CCO:MP0005634
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0001552	increased circulating triglyceride level	CCO:MP0001552
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0001554	increased circulating free fatty acid level	CCO:MP0001554
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0002575	increased circulating ketone body level	CCO:MP0002575
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0001560	abnormal circulating insulin level	CCO:MP0001560
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0000179	abnormal blood chemistry	CCO:MP0000179
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0002118	abnormal lipid homeostasis	CCO:MP0002118
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0002628	hepatic steatosis	CCO:MP0002628
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0005068	abnormal NK cell morphology	CCO:MP0005068
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0002581	abnormal ileum morphology	CCO:MP0002581
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0001657	abnormal induced morbidity/mortality	CCO:MP0001657
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0005232	abnormal mesenteric lymph node morphology	CCO:MP0005232
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0005606	increased bleeding time	CCO:MP0005606
MGI:1889549	Txnip	Txnip<tm1Jjy>/Txnip<tm1Jjy>	involves: C57BL/6 * CBA	MP:0003606	kidney failure	CCO:MP0003606
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0005069	abnormal NK cell physiology	CCO:MP0005069
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0005013	increased lymphocyte cell number	CCO:MP0005013
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0005348	increased T cell proliferation	CCO:MP0005348
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0004973	increased regulatory T cell number	CCO:MP0004973
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0008040	decreased NK T cell number	CCO:MP0008040
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0008045	decreased NK cell number	CCO:MP0008045
MGI:1889549	Txnip	Txnip<tm1Yu>/Txnip<tm1Yu>	involves: 129/Sv	MP:0008079	decreased CD8-positive T cell number	CCO:MP0008079
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0002085	abnormal embryonic tissue morphology	CCO:MP0002085
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0003693	abnormal embryo hatching	CCO:MP0003693
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0004957	abnormal blastocyst morphology	CCO:MP0004957
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0003988	disorganized embryonic tissue	CCO:MP0003988
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0006042	increased apoptosis	CCO:MP0006042
MGI:1341217	Uba3	Uba3<tm1Tchi>/Uba3<tm1Tchi>	involves: C57BL/6 * CBA	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0008280	male germ cell apoptosis	CCO:MP0008280
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0009230	abnormal sperm head morphology	CCO:MP0009230
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0002675	asthenozoospermia	CCO:MP0002675
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	MP:0001925	male infertility	CCO:MP0001925
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0001925	male infertility	CCO:MP0001925
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	involves: 129P2/OlaHsd * FVB/NJ	MP:0005578	teratozoospermia	CCO:MP0005578
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	MP:0008966	abnormal chiasmata formation	CCO:MP0008966
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	MP:0005169	abnormal male meiosis	CCO:MP0005169
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	MP:0001156	abnormal spermatogenesis	CCO:MP0001156
MGI:102944	Ube2b	Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>	either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N)	MP:0006379	abnormal spermatocyte morphology	CCO:MP0006379
MGI:102944	Ube2b	"Ube2a<tm1Agr>/Ube2a<tm1Agr>,Ube2b<tm1Jhjh>/Ube2b<+>"	involves: 129P2/OlaHsd * FVB/N	MP:0001262	decreased body weight	CCO:MP0001262
MGI:102944	Ube2b	"Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<+>"	involves: 129P2/OlaHsd * FVB/N	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:102944	Ube2b	"Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<+>"	involves: 129P2/OlaHsd * FVB/N	MP:0001262	decreased body weight	CCO:MP0001262
MGI:102944	Ube2b	"Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<+>"	involves: 129P2/OlaHsd * FVB/N	MP:0004200	decreased fetal size	CCO:MP0004200
MGI:102944	Ube2b	"Ube2a<tm1Agr>/Ube2a<tm1Agr>,Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>"	involves: 129P2/OlaHsd * FVB/N	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:102944	Ube2b	"Ube2a<tm1Agr>/Y,Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>"	involves: 129P2/OlaHsd * FVB/N	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:102944	Ube2b	"Ube2a<tm1Agr>/Ube2a<tm1Agr>,Ube2b<tm1Jhjh>/Ube2b<+>"	involves: 129P2/OlaHsd * FVB/N	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:102944	Ube2b	"Ube2a<tm1Agr>/Ube2a<+>,Ube2b<tm1Jhjh>/Ube2b<tm1Jhjh>"	involves: 129P2/OlaHsd * FVB/N	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:107365	Ube2i	Ube2i<tm1.1Adej>/Ube2i<+>	involves: 129S1/Sv * BALB/c * C57BL/6	MP:0002429	abnormal blood cell morphology/development	CCO:MP0002429
MGI:107365	Ube2i	Ube2i<tm1.1Adej>/Ube2i<tm1.1Adej>	involves: 129S1/Sv * BALB/c * C57BL/6	MP:0004965	inner cell mass degeneration	CCO:MP0004965
MGI:107365	Ube2i	Ube2i<tm1.1Adej>/Ube2i<tm1.1Adej>	involves: 129S1/Sv * BALB/c * C57BL/6	MP:0006205	embryonic lethality before somite formation	CCO:MP0006205
MGI:107365	Ube2i	Ube2i<tm1.1Adej>/Ube2i<tm1.1Adej>	involves: 129S1/Sv * BALB/c * C57BL/6	MP:0002718	abnormal inner cell mass	CCO:MP0002718
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0001730	embryonic growth arrest	CCO:MP0001730
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0001614	abnormal blood vessel morphology	CCO:MP0001614
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0003400	kinked neural tube	CCO:MP0003400
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0004261	abnormal embryonic neuroepithelium morphology	CCO:MP0004261
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0000281	abnormal ventricular septum morphology	CCO:MP0000281
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0002190	disorganized myocardium	CCO:MP0002190
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0000282	abnormal atrial septum morphology	CCO:MP0000282
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0002189	abnormal myocardial trabeculae morphology	CCO:MP0002189
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0000267	abnormal heart development	CCO:MP0000267
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0001914	hemorrhage	CCO:MP0001914
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0002151	abnormal neural tube morphology/development	CCO:MP0002151
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0001722	pale yolk sac	CCO:MP0001722
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0003232	abnormal forebrain development	CCO:MP0003232
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0003229	abnormal vitelline vasculature	CCO:MP0003229
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0006008	abnormal neurogenesis	CCO:MP0006008
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0003105	abnormal heart atrium morphology	CCO:MP0003105
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0005312	pericardial effusion	CCO:MP0005312
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0005294	abnormal heart ventricle morphology	CCO:MP0005294
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0000292	distended pericardial sacs	CCO:MP0000292
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0001698	decreased embryo size	CCO:MP0001698
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0000266	abnormal heart morphology	CCO:MP0000266
MGI:1861099	Ubr2	"Ubr1<tm1Avar>/Ubr1<tm1Avar>,Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>"	involves: 129S1/Sv * C57BL/6	MP:0004076	abnormal vitelline vascular remodeling	CCO:MP0004076
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	129S1/Sv	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	129S1/Sv	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * CD-1	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * CD-1	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0008261	arrest of male meiosis	CCO:MP0008261
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0003205	testicular atrophy	CCO:MP0003205
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0002687	oligozoospermia	CCO:MP0002687
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0001925	male infertility	CCO:MP0001925
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0002161	abnormal fertility/fecundity	CCO:MP0002161
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0001929	abnormal gametogenesis	CCO:MP0001929
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0002080	prenatal lethality	CCO:MP0002080
MGI:1861099	Ubr2	Ubr2<tm1Ytkw>/Ubr2<tm1Ytkw>	involves: 129S1/Sv * C57BL/6	MP:0001923	reduced female fertility	CCO:MP0001923
MGI:2445092	Utp14b	Utp14b<jsd>/Utp14b<jsd>	involves: C3H/HeJ * C57BL/6J	MP:0001925	male infertility	CCO:MP0001925
MGI:2445092	Utp14b	Utp14b<jsd>/Utp14b<jsd>	involves: C3H/HeJ * C57BL/6J	MP:0005159	azoospermia	CCO:MP0005159
MGI:2445092	Utp14b	Utp14b<jsd>/Utp14b<jsd>	involves: C3H/HeJ * C57BL/6J	MP:0004852	decreased testis weight	CCO:MP0004852
MGI:2442543	Vash1	Vash1<tm1Ysat>/Vash1<tm1Ysat>	involves: C57BL/6	MP:0005601	increased angiogenesis	CCO:MP0005601
MGI:2442543	Vash1	Vash1<tm1Ysat>/Vash1<+>	involves: C57BL/6	MP:0005601	increased angiogenesis	CCO:MP0005601
MGI:1926395	Wtap	Wtap<Gt(ROSANBetageo)5B4Masn>/Wtap<Gt(ROSANBetageo)5B4Masn>	involves: 129P2/OlaHsd	MP:0001672	abnormal embryogenesis/ development	CCO:MP0001672
MGI:1926395	Wtap	Wtap<Gt(ROSANBetageo)5B4Masn>/Wtap<Gt(ROSANBetageo)5B4Masn>	involves: 129P2/OlaHsd	MP:0006207	embryonic lethality during organogenesis	CCO:MP0006207
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<tm1Ecf>	involves: 129 * C57BL/6	MP:0002048	lung adenoma	CCO:MP0002048
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<+>	involves: 129 * SKH1	MP:0001203	increased sensitivity to skin irradiation	CCO:MP0001203
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<tm1Ecf>	involves: 129 * SKH1	MP:0001203	increased sensitivity to skin irradiation	CCO:MP0001203
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<tm1Ecf>	involves: 129 * SKH1	MP:0001222	epidermal hyperplasia	CCO:MP0001222
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<tm1Ecf>	involves: 129 * SKH1	MP:0000377	abnormal hair follicle morphology	CCO:MP0000377
MGI:103557	Xpc	"Mc1r<e>/Mc1r<e>,Xpc<tm1Brd>/Xpc<tm1Brd>,Tg(KRT14-Kitl)1Takk/0"	involves: 129S7/SvEvBrd * C57BL/6 * SJL	MP:0001212	skin lesions	CCO:MP0001212
MGI:103557	Xpc	Xpc<tm1Brd>/Xpc<tm1Brd>	involves: 129S7/SvEvBrd * C57BL	MP:0001999	photosensitivity	CCO:MP0001999
MGI:103557	Xpc	Xpc<tm1Brd>/Xpc<tm1Brd>	involves: 129S7/SvEvBrd * C57BL	MP:0001203	increased sensitivity to skin irradiation	CCO:MP0001203
MGI:103557	Xpc	Xpc<tm1Brd>/Xpc<tm1Brd>	involves: 129S7/SvEvBrd * C57BL	MP:0005621	abnormal cell physiology	CCO:MP0005621
MGI:103557	Xpc	Xpc<tm1Brd>/Xpc<tm1Brd>	involves: 129S7/SvEvBrd * C57BL	MP:0004501	increased incidence of UV-induced tumors	CCO:MP0004501
MGI:103557	Xpc	"Mc1r<e>/Mc1r<e>,Xpc<tm1Brd>/Xpc<tm1Brd>,Tg(KRT14-Kitl)1Takk/0"	involves: 129S7/SvEvBrd * C57BL/6 * SJL	MP:0001263	weight loss	CCO:MP0001263
MGI:103557	Xpc	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0002083	premature death	CCO:MP0002083
MGI:103557	Xpc	"Mc1r<e>/Mc1r<e>,Xpc<tm1Brd>/Xpc<tm1Brd>,Tg(KRT14-Kitl)1Takk/0"	involves: 129S7/SvEvBrd * C57BL/6 * SJL	MP:0001219	thickened epidermis	CCO:MP0001219
MGI:103557	Xpc	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0008014	lung tumor	CCO:MP0008014
MGI:103557	Xpc	"Mc1r<e>/Mc1r<e>,Xpc<tm1Brd>/Xpc<tm1Brd>,Tg(KRT14-Kitl)1Takk/0"	involves: 129S7/SvEvBrd * C57BL/6 * SJL	MP:0004207	squamous cell carcinoma	CCO:MP0004207
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<tm1Ecf>	involves: 129 * C57BL/6	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<tm1Ecf>	involves: 129 * C57BL/6	MP:0008014	lung tumor	CCO:MP0008014
MGI:103557	Xpc	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0002027	lung adenocarcinoma	CCO:MP0002027
MGI:103557	Xpc	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0002048	lung adenoma	CCO:MP0002048
MGI:103557	Xpc	"Gadd45a<tm1Ajf>/Gadd45a<tm1Ajf>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129X1/SvJ * C57BL/6)	MP:0001272	increased metastatic potential	CCO:MP0001272
MGI:103557	Xpc	"Mc1r<e>/Mc1r<e>,Xpc<tm1Brd>/Xpc<tm1Brd>,Tg(KRT14-Kitl)1Takk/0"	involves: 129S7/SvEvBrd * C57BL/6 * SJL	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:103557	Xpc	"Ercc6<tm1Gvh>/Ercc6<tm1Gvh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0002427	disproportionate dwarf	CCO:MP0002427
MGI:103557	Xpc	"Ercc6<tm1Gvh>/Ercc6<tm1Gvh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0008410	increased cellular sensitivity to ultraviolet irradiation	CCO:MP0008410
MGI:103557	Xpc	"Ercc6<tm1Gvh>/Ercc6<tm1Gvh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0008058	abnormal DNA repair	CCO:MP0008058
MGI:103557	Xpc	"Ercc6<tm1Gvh>/Ercc6<tm1Gvh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0005150	cachexia	CCO:MP0005150
MGI:103557	Xpc	"Ercc6<tm1Gvh>/Ercc6<tm1Gvh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0001732	postnatal growth retardation	CCO:MP0001732
MGI:103557	Xpc	"Ercc6<tm1Gvh>/Ercc6<tm1Gvh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0002081	perinatal lethality	CCO:MP0002081
MGI:103557	Xpc	"Ercc6<tm1Gvh>/Ercc6<tm1Gvh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129 * 129P2/OlaHsd * C57BL/6J	MP:0002082	postnatal lethality	CCO:MP0002082
MGI:103557	Xpc	"Apex1<tm1Ecf>/Apex1<+>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129	MP:0003674	oxidative stress	CCO:MP0003674
MGI:103557	Xpc	"Ercc8<tm1Jhjh>/Ercc8<tm1Jhjh>,Xpc<tm1Ecf>/Xpc<+>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0004501	increased incidence of UV-induced tumors	CCO:MP0004501
MGI:103557	Xpc	"Apex1<tm1Ecf>/Apex1<+>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129	MP:0002020	increased tumor incidence	CCO:MP0002020
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<tm1Ecf>	involves: 129	MP:0008410	increased cellular sensitivity to ultraviolet irradiation	CCO:MP0008410
MGI:103557	Xpc	Xpc<tm1Ecf>/Xpc<tm1Ecf>	involves: 129	MP:0003674	oxidative stress	CCO:MP0003674
MGI:103557	Xpc	"Ercc8<tm1Jhjh>/Ercc8<tm1Jhjh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0001265	decreased body size	CCO:MP0001265
MGI:103557	Xpc	"Ercc8<tm1Jhjh>/Ercc8<tm1Jhjh>,Xpc<tm1Ecf>/Xpc<tm1Ecf>"	involves: 129P2/OlaHsd * C57BL/6J	MP:0002083	premature death	CCO:MP0002083
MGI:1914233	Zfp830	Zfp830<tm1Cota>/Zfp830<tm1Cota>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6N)	MP:0006204	embryonic lethality before implantation	CCO:MP0006204
MGI:1914233	Zfp830	Zfp830<tm1Cota>/Zfp830<tm1Cota>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6N)	MP:0001728	failure of embryo implantation	CCO:MP0001728
MGI:1914233	Zfp830	Zfp830<tm1Cota>/Zfp830<tm1Cota>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6N)	MP:0005028	abnormal trophectoderm morphology	CCO:MP0005028
MGI:1914233	Zfp830	Zfp830<tm1Cota>/Zfp830<tm1Cota>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6N)	MP:0003694	failure to hatch from the zona pellucida	CCO:MP0003694
MGI:1914233	Zfp830	Zfp830<tm1Cota>/Zfp830<tm1Cota>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6N)	MP:0003077	abnormal cell cycle	CCO:MP0003077
MGI:1914233	Zfp830	Zfp830<tm1Cota>/Zfp830<tm1Cota>	either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6N)	MP:0002718	abnormal inner cell mass	CCO:MP0002718