12363 genotypes with 23634 annotations displayed
of selected term and subterms
|
Searched Term: cellular phenotype
|
917M/917M+
(C57BL/6-917M)
|
decreased osteoblast proliferation
|
J:99483
|
1700010I14Rikem1Osb/1700010I14Rikem1Osb
(involves: C57BL/6J * DBA/2J)
|
decreased hyperactivated sperm motility
|
J:340908
|
decreased sperm progressive motility
|
J:340908
|
1700010I14Rikem1Osb/1700010I14Rikem1Osb Tsnaxip1em1Osb/Tsnaxip1em1Osb
(involves: C57BL/6J * DBA/2J)
|
decreased hyperactivated sperm motility
|
J:340908
|
decreased sperm progressive motility
|
J:340908
|
1700028K03Rikem1Jzc/1700028K03Rikem1Jzc
(C57BL/6-1700028K03Rikem1Jzc)
|
abnormal double-strand DNA break repair
|
J:285969
|
abnormal female meiosis I arrest
|
J:285969
|
absent oocytes
|
J:285969
|
arrest of male meiosis
|
J:285969
|
azoospermia
|
J:285969
|
decreased oocyte number
|
J:285969
|
increased male germ cell apoptosis
|
J:285969
|
1700102P08Rikem1Feis/1700102P08Rikem1Feis
(C57BL/6-1700102P08Rikem1Feis)
|
arrest of male meiosis
|
J:301139
|
azoospermia
|
J:301139
|
increased male germ cell apoptosis
|
J:301139
|
2310065F04Riktm1.1Boet/2310065F04Riktm1.1Boet
(involves: C57BL/6 * SJL)
|
increased skeletal muscle satellite cell proliferation
|
J:306156
|
2500002B13RikGt(Ayu21-T167)Imeg/2500002B13RikGt(Ayu21-T167)Imeg
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal mitochondrial physiology
|
J:311513
|
2500002B13Riktm1(CAG-2500002B13Rik)Yo/2500002B13Rik+
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
increased mitochondrial number
|
J:311513
|
2610005L07RikGt(ROSA)73Sor/2610005L07RikGt(ROSA)73Sor
(involves: 129S4/SvJaeSor)
|
increased fibroblast cell migration
|
J:117491
|
2700049A03Riktm1.1Arte/2700049A03Riktm1.1Arte Tg(Prrx1-cre)1Cjt/0
(involves: C57BL/6J * C57BL/6NTac * SJL/J)
|
abnormal cilium morphology
|
J:175541
|
decreased fibroblast cell migration
|
J:175541
|
2700049A03Riktm1.2Arte/2700049A03Riktm1.2Arte
(either: (involves: C57BL/6NTac) or (involves: C57BL/6NTac * CD-1))
|
abnormal centrosome morphology
|
J:175541
|
absent embryonic cilia
|
J:175541
|
2700049A03Riktm1Blnw/2700049A03Riktm1Blnw
(Not Specified)
|
abnormal cell morphology
|
J:220629
|
abnormal cilium morphology
|
J:220629
|
4930447C04Rikem1Amp/4930447C04Rikem1Amp
(involves: C57BL/6J * CBA/J)
|
abnormal chiasmata formation
|
J:238491
|
abnormal chromosomal synapsis
|
J:238491
|
abnormal male meiosis
|
J:238491
|
abnormal meiosis
|
J:238491
|
abnormal oogenesis
|
J:238491
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:238491
|
absent oocytes
|
J:238491
|
arrest of male meiosis
|
J:238491
|
azoospermia
|
J:238491
|
increased male germ cell apoptosis
|
J:238491
|
4930463O16Rikem1Bmpe/4930463O16Rikem1Bmpe
(C57BL/6N-4930463O16Rikem1Bmpe)
|
abnormal sperm flagellum morphology
|
J:328509
|
abnormal sperm motility
|
J:328509
|
increased sperm motility
|
J:328509
|
increased sperm progressive motility
|
J:328509
|
oligozoospermia
|
J:328509
|
4930567H17Rikem1JbmuGm14725em1Jbmu/Y
(B6(SJL)-4930567H17Rikem1Jbmu Gm14725em1Jbmu/Jbmu)
|
teratozoospermia
|
J:334464
|
4930590J08Rikem1Qsh/4930590J08Rikem1Qsh
(C57BL/6-4930590J08Rikem1Qsh)
|
abnormal cellular respiration
|
J:333195
|
abnormal oxidative phosphorylation
|
J:333195
|
asthenozoospermia
|
J:333195
|
decreased male germ cell number
|
J:333195
|
decreased sperm progressive motility
|
J:333195
|
increased testis apoptosis
|
J:333195
|
oligozoospermia
|
J:333195
|
4933427D14Riktm1.1(KOMP)Vlcg/4933427D14Riktm1.1(KOMP)Vlcg
(C57BL/6N-4933427D14Riktm1.1(KOMP)Vlcg/JMmucd)
|
abnormal primary cilium morphology
|
J:307969
|
decreased embryonic neuroepithelium primary cilium number
|
J:307969
|
a/a Hps6ru/Hps6ru
(B6.Cg-Hps6ru)
|
decreased platelet ATP level
|
J:7327
|
A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ Clk4em1Yihc/Clk4em1Yihc
(B6(FVB)-Clk4em1Yihc A1cfTg(Myh6-cre/Esr1*)1Jmk)
|
cardiac interstitial fibrosis
|
J:327369
|
A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ Dusp12em1Zhzy/Dusp12em1Zhzy
(involves: FVB/N)
|
increased cellular sensitivity to oxidative stress
|
J:345360
|
A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ Tg(CAG-DMPK*)1323Coop/0
(involves: FVB)
|
cardiac interstitial fibrosis
|
J:127391
|
A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+ Tg(Myh6-2A)#Know/0
(involves: BALB/c * C57BL/6 * FVB/N)
|
cardiac interstitial fibrosis
|
J:128060
|
A1cftm1Ddsn/A1cftm1Ddsn
(involves: 129X1/SvJ)
|
decreased cell proliferation
|
J:114732
|
A4gnttm1Jnaka/A4gnttm1Jnaka
(B6.129S6-A4gnttm1Jnaka)
|
increased cell proliferation
|
J:184485
|
A930011O12Rik/Mir124a-1tm1Tfur/A930011O12Rik/Mir124a-1tm1Tfur
(involves: 129S6/SvEvTac)
|
abnormal retina apoptosis
|
J:179784
|
increased neuron apoptosis
|
J:179784
|
Aiapy/?
(involves: C3H/HeJ * C57BL/6J)
|
maternal effect
|
J:18848
|
am-J/am-J
(involves: C3H/HeJ * C57BL/6J)
|
maternal imprinting
|
J:16570
|
am/a
(involves: 101/Rl * C3H/Rl)
|
maternal effect
|
J:5964
|
Avy/a
(involves: C3H/HeJ * C57BL/6)
|
abnormal epigenetic regulation of gene expression
|
J:117156
|
Avy/a
(involves: C57BL/6J)
|
abnormal epigenetic regulation of gene expression
|
J:82396
|
Avy/a Axin1Fu/Axin1+
(involves: 129P4/RrRk * C67BL/6J)
|
genetic imprinting
|
J:82396
|
Ay/Ay
(101-Ay)
|
maternal effect
|
J:174504
|
AA467197em1Nyam/AA467197em1Nyam
(C57BL/6J-AA467197em1Nyam)
|
abnormal mitochondrial physiology
|
J:347271
|
impaired autophagy
|
J:347271
|
increased cellular ATP level
|
J:347271
|
increased cellular sensitivity to hydrogen peroxide
|
J:347271
|
AA467197em1Nyam/AA467197em1Nyam Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: C57BL/6J * C57BL/6NCrlj * DBA/2)
|
impaired autophagy
|
J:347271
|
Aaastm1Ahue/Aaastm1Ahue
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:106908
|
AabprNZB/Slc/?
(involves: NZB/Slc * NZW/Slc)
|
increased B cell proliferation
|
J:87690
|
Aars1sti/Aars1tm1Slac
(involves: C57BL/6J)
|
abnormal autophagy
|
J:216802
|
abnormal myocardial fiber mitochondrial morphology
|
J:216802
|
cardiac interstitial fibrosis
|
J:216802
|
AatfGt(pGT1.8geo)3Pgr/AatfGt(pGT1.8geo)3Pgr
(either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * NMRI))
|
abnormal intracellular organelle morphology
|
J:65741
|
abnormal ribosome morphology
|
J:65741
|
decreased cell proliferation
|
J:65741
|
Abattm1c(EUCOMM)Hmgu/Abattm1c(EUCOMM)Hmgu Tg(Cd4-cre)1Cwi/0
(involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * DBA/2)
|
decreased T cell proliferation
|
J:333883
|
Abca1tm1Jdm/Abca1tm1Jdm
(DBA/1LacJ-Abca1tm1Jdm)
|
impaired macrophage phagocytosis
|
J:63265
|
Abca1tm1Jdm/Abca1tm1Jdm
(involves: DBA/1LacJ)
|
decreased cholesterol efflux
|
J:89906
|
oligozoospermia
|
J:89906
|
Abca1tm1Jdm/Abca1tm1Jdm
(DBA/1-Abca1tm1Jdm/J)
|
increased cholesterol efflux
|
J:130777
|
Abca1tm1Jdm/Abca1tm1Jdm
(involves: C57BL/6 * DBA/1LacJ)
|
impaired macrophage phagocytosis
|
J:132254
|
Abca1tm1Jdm/Abca1tm1Jdm Abcg1tm1Dgen/Abcg1tm1Dgen
(involves: 129P2/OlaHsd * C57BL/6 * DBA/1LacJ)
|
decreased cholesterol efflux
|
J:130777
|
Abca1tm1Jdm/Abca1tm1Jdm Tgm2tm1Gml/Tgm2tm1Gml
(involves: C57BL/6 * DBA/1LacJ)
|
impaired macrophage phagocytosis
|
J:132254
|
Abca1tm1Jp/Abca1tm1Jp Tg(Vil1-cre)997Gum/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
decreased cholesterol efflux
|
J:107802
|
Abca12el12/Abca12+
(involves: 129/Sv * C57BL/6)
|
decreased cholesterol efflux
|
J:161652
|
Abca12el12/Abca12el12
(involves: 129/Sv * C57BL/6)
|
decreased cholesterol efflux
|
J:161652
|
Abca13em1Kueda/Abca13em1Kueda
(C57BL/6N-Abca13em1Kueda/Kueda)
|
abnormal synaptic vesicle endocytosis
|
J:304162
|
Abcb4tm1Bor/Abcb4tm1Bor Portm1Wolf/Portm1Wolf Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129P2/OlaHsd * C57BL/6 * DBA * FVB/N)
|
increased hepatocyte proliferation
|
J:215915
|
Abcb5tm1.2Nyf/Abcb5tm1.2Nyf
(involves: 129S6/SvEvTac * C57BL/6)
|
increased cell proliferation
|
J:213708
|
Abcb6tm1Jsch/Abcb6tm1Jsch
(involves: 129)
|
abnormal mitochondrial physiology
|
J:184574
|
Abcb7tm1.1Mdf/Abcb7+
(involves: 129S4/SvJae * FVB)
|
genetic imprinting
|
J:106838
|
Abcb7tm1Mdf/Y Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(either: B6.Cg-Speer6-ps1Tg(Alb-cre)21Mgn Abcb7tm1Mdf or (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA))
|
abnormal hepatocyte mitochondrial morphology
|
J:106838
|
Abcb10tm1.1Tafu/Abcb10tm1.2Tafu Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6J * C57BL/6NCrlj * CBA/J * CBA/JNCrlJ)
|
abnormal mitochondrial morphology
|
J:223428
|
Abcb10tm1.2Tafu/Abcb10tm1.2Tafu
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
oxidative stress
|
J:223428
|
Abcb10tm1Lex/Abcb10+
(involves: 129S/SvEvBrd * C57BL/6)
|
abnormal mitochondrial physiology
|
J:189396
|
oxidative stress
|
J:189396
|
Abcc5tm1Bor/Abcc5tm1Bor
(involves: 129P2/OlaHsd * FVB)
|
cellular phenotype
|
J:135561
|
Abcc9tm1.1Mcn/Abcc9tm1.1Mcn Tg(Tagln-cre)1Her/0
(involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial physiology
|
J:216539
|
abnormal myocardial fiber mitochondrial morphology
|
J:216539
|
decreased fatty acid oxidation
|
J:216539
|
decreased mitochondrial size
|
J:216539
|
increased cellular sensitivity to hydrogen peroxide
|
J:216539
|
oxidative stress
|
J:216539
|
Abcc9tm1Cfb/Abcc9tm1Cfb
(involves: CD-1)
|
increased skeletal muscle cell glucose uptake
|
J:71840
|
Abcd3tm1Safe/Abcd3tm1Safe
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal peroxisome morphology
|
J:217065
|
Abcg1tm1Dgen/Abcg1+ Abcg4tm1Dgen/Abcg4tm1Dgen
(involves: 129P2/OlaHsd)
|
decreased cholesterol efflux
|
J:141549
|
Abcg1tm1Dgen/Abcg1tm1Dgen
(B6.129P2-Abcg1tm1Dgen)
|
increased macrophage derived foam cell number
|
J:117028
|
Abcg1tm1Dgen/Abcg1tm1Dgen
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal monocyte differentiation
|
J:132952
|
decreased cholesterol efflux
|
J:130777
|
Abcg1tm1Dgen/Abcg1tm1Dgen Abcg4tm1Dgen/Abcg4+
(involves: 129P2/OlaHsd)
|
decreased cholesterol efflux
|
J:141549
|
Abcg1tm1Dgen/Abcg1tm1Dgen Abcg4tm1Dgen/Abcg4tm1Dgen
(involves: 129P2/OlaHsd)
|
decreased cholesterol efflux
|
J:141549
|
Abcg2tm1.1Ssf/Abcg2tm1.1Ssf
(involves: 129 * C57BL/6 * FVB)
|
abnormal endoplasmic reticulum morphology
|
J:201884
|
abnormal hepatocyte mitochondrial morphology
|
J:201884
|
abnormal mitochondrial crista morphology
|
J:201884
|
abnormal mitochondrial physiology
|
J:201884
|
abnormal oxidative phosphorylation
|
J:201884
|
abnormal respiratory electron transport chain
|
J:201884
|
oxidative stress
|
J:201884
|
Abcg5tm1.1Hobb/Abcg5tm1.1Hobb Abcg8tm1.1Hobb/Abcg8tm1.1Hobb Speer6-ps1Tg(Alb-cre)21Mgn/?
(involves: C57BL/6 * DBA * SJL)
|
abnormal cellular cholesterol metabolism
|
J:215443
|
decreased cholesterol efflux
|
J:215443
|
Abcg5tm1.1Hobb/Abcg5tm1.1Hobb Abcg8tm1.1Hobb/Abcg8tm1.1Hobb Tg(CAG-cre/Esr1*)5Amc/?
(involves: C57BL/6 * CBA * SJL)
|
abnormal cellular cholesterol metabolism
|
J:215443
|
decreased cholesterol efflux
|
J:215443
|
Abcg5tm1.1Hobb/Abcg5tm1.1Hobb Abcg8tm1.1Hobb/Abcg8tm1.1Hobb Tg(Vil1-cre)997Gum/?
(involves: C57BL/6 * SJL)
|
abnormal cellular cholesterol metabolism
|
J:215443
|
decreased cholesterol efflux
|
J:215443
|
Abcg5trac/Abcg5trac
(A/J-Abcg5trac)
|
abnormal megakaryocyte differentiation
|
J:157223
|
Abhd2em1Lshko/Abhd2+
(C57BL/6N-Abhd2em1Lshko)
|
increased granulosa cell apoptosis
|
J:322075
|
Abhd2em1Lshko/Abhd2em1Lshko
(C57BL/6N-Abhd2em1Lshko)
|
increased granulosa cell apoptosis
|
J:322075
|
Abhd2Gt(pUHachi)8025Imeg/Abhd2Gt(pUHachi)8025Imeg
(involves: C57BL/6NCrj * CBA/JNCrj)
|
abnormal cell migration
|
J:96209
|
Abhd5tm1.1Lqyu/Abhd5tm1.1Lqyu Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA)
|
decreased fatty acid oxidation
|
J:199570
|
oxidative stress
|
J:199570
|
Abhd5tm1.1Rze/Abhd5tm1.1Rze
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:160725
|
Abhd5tm1Rze/Abhd5tm1Rze Tg(Ckmm-cre)5Khn/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB)
|
increased cardiac muscle cell glucose uptake
|
J:197835
|
Abhd6tm1a(EUCOMM)Hmgu/Abhd6tm1a(EUCOMM)Hmgu
(C57BL/6N-Abhd6tm1a(EUCOMM)Hmgu)
|
increased adipocyte glucose uptake
|
J:234876
|
increased fatty acid beta-oxidation
|
J:234876
|
increased skeletal muscle cell glucose uptake
|
J:234876
|
Abi1tm1Pen/Abi1+ Abi2tm1Pen/Abi2tm1Pen
(Not Specified)
|
decreased T cell proliferation
|
J:104623
|
Abi1tm1Pen/Abi1tm1Pen Abi2tm1Pen/Abi2+
(Not Specified)
|
abnormal cell physiology
|
J:169009
|
Abi3bptm1Tac/Abi3bptm1Tac
(involves: 129S5/SvEvBrd)
|
abnormal cell differentiation
|
J:251000
|
increased cell proliferation
|
J:251000
|
Abl1tm1Mlg/Abl1tm1Mlg
(B6.129-Abl1tm1Mlg)
|
increased fetal cardiomyocyte proliferation
|
J:156743
|
Abl1tm1Mlg/Abl1tm1Mlg Abl2tm1Ajk/Abl2tm1Ajk
(involves: 129S/SvEv * 129S4/SvJae * C57BL/6J)
|
abnormal actin cytoskeleton morphology
|
J:51887
|
abnormal neuron differentiation
|
J:51887
|
increased embryonic tissue cell apoptosis
|
J:51887
|
Abl1tm2.1Goff/Abl1tm2.1Goff Abl2tm1Ajk/Abl2tm1Ajk Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * C57BL/6J * SJL)
|
decreased cerebellar granule cell precursor proliferation
|
J:166211
|
Abrtm1Jhg/Abrtm1Jhg Bcrtm1Hkp/Bcrtm1Hkp
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * Black Swiss * C57BL/6)
|
abnormal radial glial cell morphology
|
J:72425
|
Abraxas1tm1.1Bwng/Abraxas1tm1.1Bwng
(involves: 129S6/SvEvTac * C57BL/6NCrl * FVB/N)
|
abnormal cell nucleus morphology
|
J:269823
|
abnormal double-strand DNA break repair
|
J:269823
|
increased cellular sensitivity to DNA damaging agents
|
J:269823
|
increased cellular sensitivity to gamma-irradiation
|
J:269823
|
spontaneous chromosome breakage
|
J:269823
|
Abraxas2tm1.2Bwng/Abraxas2tm1.2Bwng
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCrl)
|
abnormal cell nucleus morphology
|
J:245949
|
abnormal chromosome morphology
|
J:245949
|
abnormal DNA replication
|
J:245949
|
abnormal mitosis
|
J:245949
|
cellular phenotype
|
J:245949
|
chromosomal instability
|
J:245949
|
increased cellular sensitivity to DNA damaging agents
|
J:245949
|
increased cellular sensitivity to ultraviolet irradiation
|
J:245949
|
Abshq1PWK/PhJ/Abshq1PWK/PhJ
(involves: LEWES/EiJ * PWK/PhJ)
|
abnormal sperm head morphology
|
J:139578
|
Abshq2PWK/PhJ/Abshq2PWK/PhJ
(involves: LEWES/EiJ * PWK/PhJ)
|
abnormal sperm head morphology
|
J:139578
|
Abshq3PWK/PhJ/Abshq3PWK/PhJ
(involves: LEWES/EiJ * PWK/PhJ)
|
abnormal sperm head morphology
|
J:139578
|
Abshq4PWK/PhJ/Abshq4PWK/PhJ
(involves: LEWES/EiJ * PWK/PhJ)
|
abnormal sperm head morphology
|
J:139578
|
Abshq5PWK/PhJ/Abshq5PWK/PhJ
(involves: LEWES/EiJ * PWK/PhJ)
|
abnormal sperm head morphology
|
J:139578
|
Abshq6PWK/PhJ/Abshq6PWK/PhJ
(involves: LEWES/EiJ * PWK/PhJ)
|
abnormal sperm head morphology
|
J:139578
|
Abshq7PWK/PhJ/Abshq7PWK/PhJ
(involves: LEWES/EiJ * PWK/PhJ)
|
abnormal sperm head morphology
|
J:139578
|
Acacatm1Dejs/Acacatm1Dejs Tg(Cd4-cre)1Cwi/? Tg(TcraTcrb)1100Mjb/?
(involves: C57BL/6 * DBA/2)
|
increased T cell proliferation
|
J:209886
|
Acacbtm1.1Dejs/Acacbtm1.1Dejs
(B6.Cg-Acacbtm1.1Dejs)
|
abnormal aerobic respiration
|
J:157000
|
increased fatty acid oxidation
|
J:157000
|
Acacbtm1Sjw/Acacbtm1Sjw
(Not Specified)
|
increased fatty acid beta-oxidation
|
J:68427
|
increased fatty acid oxidation
|
J:68427
|
Acad8m1Ytc/Acad8m1Ytc
(involves: C57BL/6)
|
abnormal hepatocyte mitochondrial morphology
|
J:222356
|
abnormal mitochondrial crista morphology
|
J:222356
|
abnormal mitochondrial matrix morphology
|
J:222356
|
abnormal mitochondrial morphology
|
J:222356
|
Acad9tm1c(KOMP)Wtsi/Acad9tm1c(KOMP)Wtsi Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6N * FVB/N)
|
abnormal mitochondrial physiology
|
J:326969
|
Acadsdel-J/Acadsdel-J
(involves: BALB/cByJ)
|
abnormal fatty acid oxidation
|
J:14707
|
Acadvltm1Vje/Acadvltm1Vje
(involves: 129/Sv * Black Swiss * C57BL/6)
|
abnormal cellular respiration
|
J:106714
|
Acbd5tm1a(EUCOMM)Wtsi/Acbd5tm1a(EUCOMM)Wtsi
(C57BL/6N-Atm1Brd Acbd5tm1a(EUCOMM)Wtsi/WtsiCnbc)
|
abnormal peroxisome morphology
|
J:299448
|
Acdtm1.1Blas/Acdtm1.1Blas Tg(KRT5-cre)1Tak/?
(involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 * SJL)
|
abnormal cell cycle
|
J:160600
|
abnormal cell cycle checkpoint function
|
J:160600
|
abnormal cell nucleus morphology
|
J:160600
|
abnormal mitosis
|
J:160600
|
decreased telomere length
|
J:160600
|
polyploidy
|
J:160600
|
Acdtm1.1Cek/Acdtm1.1Cek
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * SJL)
|
abnormal cell physiology
|
J:160503
|
abnormal chromosome morphology
|
J:160503
|
early cellular replicative senescence
|
J:160503
|
polyploidy
|
J:160503
|
Ace2em1Cya/Y
(C57BL/6J-Ace2em1Cya/Cya)
|
oxidative stress
|
J:299383
|
Ace2tm1Hira/Y
(involves: 129S7/SvEvBrd * C57BL/6)
|
cardiac interstitial fibrosis
|
J:135766
|
Ace2tm1Pngr/Y
(involves: 129P2/OlaHsd * C57BL/6)
|
oxidative stress
|
J:124548
|
Acetm1Unc/Acetm1Unc
(involves: 129P2/OlaHsd * C57BL/6J)
|
impaired sperm migration in female genital tract
|
J:46177
|
Acer1tm1a(EUCOMM)Wtsi/Acer1tm1a(EUCOMM)Wtsi
(C57BL/6N-Acer1tm1a(EUCOMM)Wtsi)
|
increased apoptosis
|
J:235775
|
increased keratinocyte proliferation
|
J:235775
|
Ackr4tm1.1Rjbn/Ackr4tm1.1Rjbn
(B6.129S6-Ackr4tm1.1Rjbn)
|
decreased T cell proliferation
|
J:166490
|
Acot11tm1Deco/Acot11tm1Deco
(involves: 129S6/SvEvTac * C57BL/6)
|
increased adipocyte glucose uptake
|
J:182660
|
increased fatty acid oxidation
|
J:182660
|
Acox1tm1Jkr/Acox1tm1Jkr
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased round spermatid number
|
J:35794
|
Acp1Gt(RRK222)Byg/Acp1Gt(RRK222)Byg
(C.129P2(B6)-Acp1Gt(RRK222)Byg)
|
decreased cardiomyocyte apoptosis
|
J:227733
|
Acp1tm1Lex/Acp1tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
increased fibroblast proliferation
|
J:171883
|
Acp2tm1Psa/Acp2tm1Psa
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6J)
|
abnormal lysosome morphology
|
J:41986
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:41986
|
Acrtm1Wen/Acrtm1Wen H1f1tm1Drab/H1f1tm1Drab Smcptm1Wen/Smcptm1Wen
(involves: 129/Sv * C57BL/6J * CD-1)
|
asthenozoospermia
|
J:98301
|
Acrtm1Wen/Acrtm1Wen H1f6tm1Drab/H1f6tm1Drab Smcptm1Wen/Smcptm1Wen
(involves: 129/Sv * C57BL/6J * CD-1)
|
abnormal sperm head morphology
|
J:98301
|
asthenozoospermia
|
J:98301
|
impaired sperm migration in female genital tract
|
J:98301
|
Acrtm1Wen/Acrtm1Wen Smcptm1Wen/Smcptm1Wen Tnp2tm1Wen/Tnp2tm1Wen
(involves: 129/Sv * C57BL/6J * CD-1)
|
asthenozoospermia
|
J:98301
|
impaired sperm migration in female genital tract
|
J:98301
|
Acrbptm1Tba/Acrbptm1Tba
(involves: 129S2/SvPas * ICR)
|
abnormal acrosome assembly
|
J:234286
|
abnormal acrosome morphology
|
J:234286
|
abnormal sperm midpiece morphology
|
J:234286
|
abnormal sperm motility
|
J:294381,
J:234286
|
abnormal sperm nucleus morphology
|
J:234286
|
asthenozoospermia
|
J:294381,
J:234286
|
decreased hyperactivated sperm motility
|
J:234286
|
decreased sperm progressive motility
|
J:294381,
J:234286
|
globozoospermia
|
J:234286
|
immotile sperm
|
J:234286
|
impaired sperm migration in female genital tract
|
J:294381
|
Acrbptm1Tba/Acrbptm1Tba Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
(involves: 129S2/SvPas * C57BL/6 * DBA/2 * ICR)
|
impaired sperm migration in female genital tract
|
J:294381
|
Acsl1tm1Rcol/Acsl1tm1Rcol Tg(Fabp4-cre)1Rev/0
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased fatty acid oxidation
|
J:162996
|
Acss1tm1Jsak/Acss1tm1Jsak
(B6.129-Acss1tm1Jsak/Jsak)
|
abnormal aerobic respiration
|
J:146647
|
Acss2em22Gpt/Acss2em22Gpt
(C57BL/6JGpt-Acss2em22Gpt/Gpt)
|
decreased pyroptosis
|
J:346990
|
Actc1tm1Jll/Actc1tm1Jll
(involves: 129P2/OlaHsd * Black Swiss)
|
increased cardiomyocyte apoptosis
|
J:102007
|
Actl6atm1.1Grc/Actl6atm1.1Grc Tg(Mx1-cre)1Cgn/0
(involves: 129S6/SvEvTac * C57BL/6J * CBA)
|
decreased hematopoietic stem cell proliferation
|
J:192124
|
Actl7aem1Fzh/Actl7aem1Fzh
(C57BL/6-Actl7aem1Fzh)
|
abnormal acrosome morphology
|
J:313844
|
detached acrosome
|
J:313844
|
Actl7btm1(KOMP)Vlcg/Actl7btm1(KOMP)Vlcg
(C57BL/6N-Actl7btm1(KOMP)Vlcg)
|
abnormal outer dense fiber morphology
|
J:334022
|
abnormal sperm annulus morphology
|
J:334022
|
abnormal sperm connecting piece morphology
|
J:334022
|
abnormal sperm flagellum morphology
|
J:334022
|
abnormal sperm head morphology
|
J:334022
|
abnormal sperm midpiece morphology
|
J:334022
|
abnormal sperm mitochondrial sheath morphology
|
J:334022
|
abnormal sperm nucleus morphology
|
J:334022
|
absent sperm mitochondrial sheath
|
J:334022
|
asthenozoospermia
|
J:334022
|
decreased sperm progressive motility
|
J:334022
|
increased male germ cell apoptosis
|
J:334022
|
oligozoospermia
|
J:334022
|
teratozoospermia
|
J:334022
|
Actl9em1Glin/Actl9em1Glin
(involves: C57BL/6J)
|
abnormal acrosome assembly
|
J:303517
|
abnormal acrosome morphology
|
J:303517
|
abnormal proacrosomal vesicle fusion
|
J:303517
|
abnormal spermatid morphology
|
J:303517
|
detached acrosome
|
J:303517
|
Actmapem1Nki/Actmapem1Nki
(FVB/N-Actmapem1Nki)
|
abnormal actin cytoskeleton morphology
|
J:331923
|
Actn2em1Kage/Actn2em1Kage
(C57BL/6-Actn2em1Kage)
|
decreased fetal cardiomyocyte proliferation
|
J:334092
|
Actn4tm1Mrpk/Actn4tm1Mrpk
(involves: 129 * C57BL/6)
|
abnormal lymphocyte chemotaxis
|
J:83911
|
abnormal podocyte adhesion
|
J:118122
|
detached podocyte
|
J:118122
|
Actrt1em1Xwei/Y
(C57BL/6-Actrt1em1Xwei)
|
abnormal spermatid morphology
|
J:311034
|
absent sperm head
|
J:311034
|
Acvr1tm1Emsh/Acvr1+
(chimera involves: BALB/c * C57BL/6 * CD-1)
|
increased apoptosis
|
J:194134
|
Acvr1tm1Vk/Acvr1tm1.1Vk H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal cardiac neural crest cell migration
|
J:90988
|
impaired cardiac neural crest cell differentiation
|
J:90988
|
Acvr1tm1Vk/Acvr1tm1.1Vk Tg(Tek-cre)12Flv/0
(involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6)
|
abnormal vascular endothelial cell differentiation
|
J:103532
|
Acvr1tm2.1Vlcg/Acvr1+ Tg(Prrx1-cre)1Cjt/0
(involves: C57BL/6J * C57BL/6NTac * SJL/J)
|
increased chondrocyte proliferation
|
J:239136
|
Acvr1btm1Enl/Acvr1btm1Enl
(either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6))
|
abnormal cell differentiation
|
J:46637
|
Acvr2atm1Hsch/Acvr2atm1Hsch Acvr2btm1Enl/Acvr2btm1Enl
(involves: 129S1/Sv * 129S4/SvJae * C57BL/6J)
|
increased embryonic epiblast cell apoptosis
|
J:57262
|
Acvr2atm1Zuk/Acvr2atm1Zuk
(either: 129 or (involves: 129S7/SvEvBrd * C57BL/6))
|
azoospermia
|
J:23924
|
Acvr2atm1Zuk/Acvr2atm1Zuk
(involves: 129S7/SvEvBrd)
|
decreased male germ cell number
|
J:71932
|
decreased round spermatid number
|
J:71932
|
decreased spermatogonia number
|
J:71932
|
Adatm1Mw/Adatm1Mw
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased hepatocyte karyomegaly
|
J:25085
|
Adatm1Mw/Adatm1Mw
(involves: 129S7/SvEvBrd)
|
increased vascular smooth muscle cell proliferation
|
J:231559
|
maternal effect
|
J:234143
|
Adatm1Mw/Adatm1Mw Tg(Afp-ADA)#Xiay/0
(involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J)
|
maternal effect
|
J:234143
|
Adad1tm1Reb/Adad1tm1Reb
(129X1/SvJ-Tenrtm1Reb)
|
asthenozoospermia
|
J:96477
|
oligozoospermia
|
J:96477
|
teratozoospermia
|
J:96477
|
Adad2em1Osb/Adad2em1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal male meiosis
|
J:337548
|
abnormal sperm head morphology
|
J:337548
|
abnormal spermatid morphology
|
J:337548
|
abnormal spermatocyte morphology
|
J:337548
|
decreased male germ cell number
|
J:337548
|
Adad2em1Shnk/Adad2em1Shnk
(C57BL/6-Adad2em1Shnk)
|
abnormal acrosome morphology
|
J:334463
|
abnormal male meiosis
|
J:334463
|
azoospermia
|
J:334463
|
Adad2em2Osb/Adad2em2Osb
(C57BL/6J-Adad2em2Osb)
|
decreased male germ cell number
|
J:337548
|
multinucleated giant male germ cells
|
J:337548
|
Adad2em2Shnk/Adad2em2Shnk
(C57BL/6-Adad2em2Shnk)
|
abnormal acrosome morphology
|
J:334463
|
abnormal male meiosis
|
J:334463
|
azoospermia
|
J:334463
|
Adad2em3(IMPC)J/Adad2em3(IMPC)J
(involves: C57BL/6NJ)
|
abnormal spermatid morphology
|
J:294176
|
azoospermia
|
J:294176
|
decreased elongated spermatid number
|
J:294176
|
Adam1atm1Tba/Adam1atm1Tba
(involves: 129S2/SvPas * ICR)
|
impaired sperm migration in female genital tract
|
J:92271
|
Adam2tm1Dgm/Adam2tm1Dgm
(involves: 129P2/OlaHsd * C57BL/6N)
|
impaired sperm migration in female genital tract
|
J:50040
|
Adam7tm1Tigm/Adam7tm1Tigm
(involves: C57BL/6)
|
abnormal sperm motility
|
J:226260
|
kinked sperm flagellum
|
J:226260
|
Adam8tm1.1Rood/Adam8tm1.1Rood
(involves: 129/Sv * C57BL/6 * FVB/N)
|
abnormal osteoclast differentiation
|
J:172936
|
Adam9tm1Bbl/Adam9tm1Bbl
(involves: 129)
|
increased keratinocyte migration
|
J:161698
|
Adam10tm1.1Khr/Adam10tm1.1Khr Csf3rtm1Link/Csf3rtm1Link Tg(Mx1-cre)1Cgn/0
(involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * C57BL/6N)
|
abnormal granulocyte differentiation
|
J:179060
|
Adam10tm1.1Khr/Adam10tm1.1Khr Tg(Mx1-cre)1Cgn/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N)
|
abnormal granulocyte differentiation
|
J:179060
|
Adam17tm1.1Srj/Adam17tm1.1Srj
(involves: 129S/SvEv * C57BL/6 * SJL)
|
abnormal enterocyte proliferation
|
J:163380
|
Adam17tm1.1Wesh/Adam17tm1.1Wesh Tg(Scgb1a1-rtTA)2Jaw/0 Tg(tetO-cre)1Jaw/0
(involves: 129 * C57BL/6 * FVB/N)
|
decreased cell proliferation
|
J:210193
|
Adam17tm1.1Wesh/Adam17tm1.1Wesh Tg(Scgb1a1-rtTA)2Jaw/0 Tg(tetO-cre)1Jaw/0 Twist2tm1.1(cre)Dor/Twist2+
(involves: 129X1/SvJ * C57BL/6 * FVB/N)
|
decreased cell proliferation
|
J:210193
|
Adam17tm1Imx/Adam17tm1Imx
(involves: 129 * C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:85547
|
Adam17tm1Imx/Adam17tm1Imx
(B6.129-Adam17tm1Imx)
|
enhanced leukocyte tethering or rolling
|
J:174865
|
Adam17tm1Rain/Adam17tm1Rain
(involves: C57BL/6)
|
enhanced leukocyte tethering or rolling
|
J:174865
|
Adamts2tm1Prc/Adamts2tm1Prc
(involves: 129)
|
oligozoospermia
|
J:69141
|
Adamts3tm1.2Itl/Adamts3tm1.2Itl
(involves: BALB/cJ * C57BL/6NTac * SJL)
|
increased hepatocyte apoptosis
|
J:245044
|
Adamts7tm1a(KOMP)Wtsi/Adamts7tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal vascular endothelial cell migration
|
J:230573
|
decreased vascular endothelial cell proliferation
|
J:230573
|
Adamts7tm1a(KOMP)Wtsi/Adamts7tm1a(KOMP)Wtsi
(C57BL/6-Adamts7tm1a(KOMP)Wtsi)
|
decreased hepatocyte proliferation
|
J:221183
|
Adamts9tm1.1Cvrk/Adamts9tm1.1Cvrk Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ Tg(Mitf-cre)7114Gsb/0
(involves: 129S6/SvEvTac * C3HeB/FeJ * C57BL/6N * CBA)
|
increased melanoblast apoptosis
|
J:262498
|
Adamts14Gt(511E11)Cmhd/Adamts14Gt(511E11)Cmhd Adamts2tm1Prc/Adamts2tm1Prc
(involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased keratinocyte apoptosis
|
J:271185
|
increased keratinocyte proliferation
|
J:271185
|
increased T cell proliferation
|
J:271185
|
Adamts18tm1.1Wzha/Adamts18tm1.1Wzha
(involves: 129 * C57BL/6)
|
decreased colon goblet cell number
|
J:258487
|
Adamts20bt-2H/Adamts20bt-2H Tg(Dct-lacZ)A12Jkn/0
(involves: C57BL/6 * CBA)
|
abnormal melanoblast migration
|
J:133403
|
Adamts20bt-Bei1/Adamts20bt-Bei1 Adamts5tm1Dgen/Adamts5tm1Dgen
(B6.Cg-Adamts20bt-Bei1 Adamts5tm1Dgen)
|
abnormal interdigital cell death
|
J:155754
|
Adamts20bt-J/Adamts20bt-J
(CBA/J-Adamts20bt-J)
|
abnormal melanoblast migration
|
J:12724
|
Adartm1.1Knk/Adartm1.1Knk
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal apoptosis
|
J:87714
|
increased embryonic tissue cell apoptosis
|
J:87714
|
increased hepatocyte apoptosis
|
J:87714
|
increased sensitivity to induced cell death
|
J:87714
|
Adartm1Knk/Adartm1Knk Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA)
|
increased hepatocyte apoptosis
|
J:87714
|
Adartm1Olds/Adartm1Olds
(involves: 129S/SvEv * C57BL/6J)
|
abnormal cell physiology
|
J:169014
|
Adck2tm1(KOMP)Vlcg/Adck2+
(C57BL/6-Adck2tm1(KOMP)Vlcg)
|
abnormal mitochondrial physiology
|
J:280282
|
decreased fatty acid beta-oxidation
|
J:280282
|
increased mitochondrial fission
|
J:280282
|
Adcy3tm1Drs/Adcy3tm1Drs
(involves: 129X1/SvJ * C57BL/6)
|
asthenozoospermia
|
J:97802
|
Adcy10tm1Lex/Adcy10tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal sperm motility
|
J:100583
|
asthenozoospermia
|
J:100583,
J:88649
|
hairpin sperm flagellum
|
J:100583
|
kinked sperm flagellum
|
J:100583
|
teratozoospermia
|
J:100583
|
Adcyap1tm1Clw/Adcyap1tm1Clw
(B6.129S4-Adcyap1tm1Clw)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:194151
|
Adgbtm1d(KOMP)Wtsi/Adgbtm1d(KOMP)Wtsi
(involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6N)
|
abnormal acrosome morphology
|
J:326350
|
abnormal sperm axoneme morphology
|
J:326350
|
abnormal sperm flagellum morphology
|
J:326350
|
abnormal sperm head morphology
|
J:326350
|
oligozoospermia
|
J:326350
|
short sperm flagellum
|
J:326350
|
Adgrf5tm1.2Bstc/Adgrf5tm1.2Bstc
(involves: 129S4/SvJae * C57BL/6J)
|
increased macrophage derived foam cell number
|
J:196943
|
Adgrg1tm1Lex/Adgrg1+
(B6.129S5-Adgrg1tm1Lex)
|
decreased male germ cell number
|
J:166517
|
Adgrg1tm1Lex/Adgrg1tm1Lex
(involves: 129 * BALB/c * C57BL/6 * FVB/N)
|
abnormal basement membrane morphology
|
J:149816
|
abnormal cerebellar granule cell migration
|
J:149816
|
abnormal radial glial cell morphology
|
J:136385
|
enhanced neuronal migration
|
J:136385
|
Adgrg2tm1Bend/Y
(involves: 129P2/OlaHsd * C57BL/6)
|
absent sperm head
|
J:93019
|
asthenozoospermia
|
J:93019
|
kinked sperm flagellum
|
J:93019
|
oligozoospermia
|
J:93019
|
teratozoospermia
|
J:93019
|
Adgrg3tm1Zgwg/Adgrg3tm1Zgwg
(involves: 129 * C57BL/6)
|
increased B cell apoptosis
|
J:222670
|
Adgrg6tm1Arte/Adgrg6tm1Arte Tg(Col2a1-cre)#Amc/0
(involves: 129S5/SvEvBrd)
|
increased chondrocyte apoptosis
|
J:224002
|
Adgrg6tm1Lex/Adgrg6tm1Lex
(involves: 129S/SvEvBrd * C57BL/6)
|
abnormal axon fasciculation
|
J:173574
|
Adgrg6tm1Taki/Adgrg6tm1Taki
(involves: C57BL/6)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:202002
|
abnormal mitochondrial crista morphology
|
J:202002
|
abnormal mitochondrial morphology
|
J:202002
|
abnormal mitochondrial shape
|
J:202002
|
Adipoqtm1Chan/Adipoq+
(B6.129-Adipoqtm1Chan)
|
increased vascular endothelial cell adhesion
|
J:122020
|
Adipoqtm1Chan/Adipoqtm1Chan
(B6.129-Adipoqtm1Chan)
|
decreased fatty acid beta-oxidation
|
J:79122
|
increased vascular endothelial cell adhesion
|
J:122020
|
Adipoqtm1Chan/Adipoqtm1Chan
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
oxidative stress
|
J:136297
|
Adipoqtm1Ish/Adipoqtm1Ish
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal osteoblast physiology
|
J:199264
|
oxidative stress
|
J:199264
|
Adipoqtm1Pesch/Adipoqtm1Pesch
(involves: C57BL/6)
|
maternal effect
|
J:219264
|
Adipoqtm1Pesch/Adipoqtm1Pesch
(B6.129S7-Adipoqtm1Pesch)
|
abnormal respiratory electron transport chain
|
J:210480
|
Adipor1tm2Tka/Adipor1tm2Tka Tg(Ckmm-cre)5Khn/0
(B6.Cg-Adipor1tm2Tka Tg(Ckmm-cre)5Khn)
|
decreased skeletal muscle fiber mitochondrial DNA content
|
J:159462
|
oxidative stress
|
J:159462
|
Adipor2tm1Dgen/Adipor2tm1Dgen
(involves: 129P2/OlaHsd * C57BL/6)
|
multinucleated giant male germ cells
|
J:101679
|
oligozoospermia
|
J:101679
|
Adissptm1c(EUCOMM)Hmgu/Adissptm1c(EUCOMM)Hmgu Tg(Adipoq-cre)1Evdr/0
(involves: C57BL/6J * C57BL/6N * FVB/NJ)
|
decreased adipocyte glucose uptake
|
J:332979
|
Adm2em1Zhan/Adm2em1Zhan
(Not Specified)
|
increased cell chemotaxis
|
J:266495
|
Admtm1Hku/Admtm1Hku
(involves: 129S6/SvEvTac * C57BL/6)
|
impaired basement membrane formation
|
J:89608
|
Admtm1Tfjt/Adm+
(involves: C57BL/6 * CBA)
|
oxidative stress
|
J:102946
|
Admtm1Unc/Admtm1Unc
(involves: 129S6/SvEvTac)
|
increased cardiomyocyte apoptosis
|
J:106927
|
increased placenta apoptosis
|
J:201446
|
Adora2btm1Kra/Adora2btm1Kra
(involves: 129 * C57BL/6J)
|
abnormal leukocyte adhesion
|
J:111715
|
abnormal leukocyte migration
|
J:111715
|
enhanced leukocyte tethering or rolling
|
J:111715
|
Adora2btm1Till/Adora2btm1Till
(B6.129P2-Adora2btm1Till)
|
abnormal cellular extravasation
|
J:125297
|
Adora3tm1(ADORA3)Msth/Adora3tm1(ADORA3)Msth
(involves: 129S7/SvEvBrd * C57BL/6J)
|
decreased mast cell degranulation
|
J:104494
|
Adora3tm1Jbsn/Adora3tm1Jbsn
(B6.129P2-Adora3tm1Jbsn)
|
abnormal mast cell degranulation
|
J:123463
|
Adra1btm1Cta/Adra1btm1Cta
(involves: 129 * C57BL/6J)
|
abnormal male germ cell apoptosis
|
J:125763
|
decreased male germ cell number
|
J:125763
|
Adra2btm1Gsb/Adra2btm1Gsb
(B6.129-Adra2btm1Gsb)
|
increased mesenchymal cell proliferation involved in lung development
|
J:166788
|
Adrb2tm1Bkk/Adrb2+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoclast differentiation
|
J:97566
|
Adrb2tm1Bkk/Adrb2tm1Bkk
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoblast physiology
|
J:97566
|
abnormal osteoclast differentiation
|
J:97566
|
Adrb2tm1Bkk/Adrb2tm1Bkk
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2 * FVB/N)
|
increased retina apoptosis
|
J:204379
|
Adrm1Gt(OST128063)Lex/Adrm1Gt(OST128063)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal male germ cell apoptosis
|
J:166694
|
abnormal oocyte morphology
|
J:166694
|
azoospermia
|
J:166694
|
decreased oocyte number
|
J:166694
|
Adtrptm1.1Clu/Adtrptm1.1Clu
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal basement membrane morphology
|
J:295059
|
abnormal extracellular matrix morphology
|
J:295059
|
Aebp1tm1Mdl/Aebp1tm1Mdl
(involves: 129S2/SvPas * C57BL/6)
|
decreased cell proliferation
|
J:70416
|
Aey30/?
(C3HeB/FeJ-Aey30)
|
oligozoospermia
|
J:82809
|
Afap1tm1.2Ycho/Afap1tm1.2Ycho
(involves: BALB/cJ * C57BL/6J)
|
maternal effect
|
J:221250
|
Afdntm1c(EUCOMM)Hmgu/Afdntm1c(EUCOMM)Hmgu Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas * C57BL/6J * C57BL/6N)
|
abnormal cell cycle
|
J:215584
|
abnormal radial glial cell morphology
|
J:215584
|
increased radial glial cell number
|
J:215584
|
Aff4tm1Nosa/Aff4tm1Nosa
(involves: 129P2/OlaHsd * C57BL/6)
|
azoospermia
|
J:100030
|
Afg3l1tm1.1Arte/Afg3l1tm1.1Arte Afg3l2tm1Arte/Afg3l2tm1Arte Gt(ROSA)26Sortm1Lrsn/Gt(ROSA)26Sor+ Tg(Plp1-cre/ERT)3Pop/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N)
|
abnormal mitochondrial physiology
|
J:237410
|
dilated mitochondrion
|
J:237410
|
Afg3l2Emv66/Afg3l2+
(involves: MEV/2Ty)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:151797
|
abnormal mitochondrial crista morphology
|
J:151797
|
abnormal mitochondrial morphology
|
J:151797
|
abnormal neuron mitochondrial morphology
|
J:151797
|
abnormal respiratory electron transport chain
|
J:151797
|
increased mitochondrial size
|
J:151797
|
oxidative stress
|
J:151797
|
Afg3l2Emv66/Afg3l2Emv66
(FVB.MEV2-Afg3l2Emv66/TyJ)
|
abnormal respiratory electron transport chain
|
J:132285
|
cellular phenotype
|
J:132285
|
Afg3l2Emv66/Afg3l2Emv66
(involves: C57BL/6 * FVB/N * MEV/2Ty)
|
abnormal mitochondrial morphology
|
J:193564
|
Afg3l2par/Afg3l2par
(Not Specified)
|
abnormal respiratory electron transport chain
|
J:132285
|
cellular phenotype
|
J:132285
|
Afg3l2tm1Arte/Afg3l2tm1Arte Gt(ROSA)26Sortm1Lrsn/Gt(ROSA)26Sor+ Tg(Pcp2-cre)2Mpin/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal Purkinje cell mitochondrial morphology
|
J:193564
|
Afg3l2tm1Arte/Afg3l2tm1Arte Gt(ROSA)26Sortm1Lrsn/Gt(ROSA)26Sor+ Tg(Plp1-cre/ERT)3Pop/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial shape
|
J:237410
|
dilated mitochondrion
|
J:237410
|
Afg3l2tm1Arte/Afg3l2tm1Arte Tg(Pcp2-cre)2Mpin/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cellular respiration
|
J:193564
|
abnormal Purkinje cell mitochondrial morphology
|
J:193564
|
Afg3l2tm1Arte/Afg3l2tm1Arte Tg(Plp1-cre/ERT)3Pop/0
(involves: C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:237410
|
increased mitochondrial size
|
J:237410
|
Agatm1Pltn/Agatm1Pltn
(involves: 129S4/SvJae * C57BL/6)
|
abnormal lysosome morphology
|
J:45587
|
Agatm1Vk/Agatm1Vk
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss)
|
abnormal lysosome morphology
|
J:49386,
J:37022,
J:91114
|
Agap2tm1.1Kye/Agap2tm1.1Kye
(involves: C57BL/6)
|
decreased mammary gland epithelial cell proliferation
|
J:158376
|
Agbl4Tn(pb-Act-RFP)1.080115015-HRAZhu/Agbl4Tn(pb-Act-RFP)1.080115015-HRAZhu
(involves: FVB/N)
|
abnormal megakaryocyte differentiation
|
J:233744
|
Agbl5tm1.1Ics/Agbl5tm1.1Ics Tg(Stra8-icre)1Reb/0
(involves: 129S2/SvPas * C57BL/6N)
|
abnormal manchette assembly
|
J:271687
|
abnormal manchette perinuclear ring morphology
|
J:271687
|
abnormal sperm axoneme morphology
|
J:271687
|
abnormal sperm nucleus morphology
|
J:271687
|
abnormal spermatid morphology
|
J:271687
|
detached acrosome
|
J:271687
|
hairpin sperm flagellum
|
J:271687
|
oligozoospermia
|
J:271687
|
Agbl5tm1.2Ics/Agbl5tm1.2Ics
(involves: 129S2/SvPas * C57BL/6N)
|
abnormal manchette assembly
|
J:271687
|
abnormal manchette disassembly
|
J:271687
|
abnormal manchette morphology
|
J:271687
|
abnormal manchette perinuclear ring morphology
|
J:271687
|
abnormal sperm axoneme morphology
|
J:271687
|
abnormal sperm fibrous sheath morphology
|
J:271687
|
abnormal sperm head morphology
|
J:271687
|
abnormal spermatid morphology
|
J:271687
|
absent sperm flagellum
|
J:271687
|
absent sperm mitochondrial sheath
|
J:271687
|
decreased elongated spermatid number
|
J:271687
|
detached acrosome
|
J:271687
|
oligozoospermia
|
J:271687
|
short sperm flagellum
|
J:271687
|
teratozoospermia
|
J:271687
|
Agertm1.1Arnd/Agertm1.1Arnd
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased vascular smooth muscle cell proliferation
|
J:82620
|
Agertm1.1Arnd/Agertm1.1Arnd
(involves: 129P2/OlaHsd)
|
decreased fibroblast chemotaxis
|
J:159873
|
Agertm1.1Hyam/Agertm1.1Hyam
(involves: 129P2/OlaHsd * C57BL/6J * CD-1)
|
abnormal cell proliferation
|
J:116507
|
decreased apoptosis
|
J:116507
|
Agfg1tm1Jvd/Agfg1tm1Jvd
(involves: 129P2/OlaHsd)
|
abnormal acroplaxome morphology
|
J:89391
|
abnormal acrosome morphology
|
J:89391
|
abnormal manchette morphology
|
J:89391
|
abnormal proacrosomal vesicle fusion
|
J:72756
|
abnormal sperm axoneme morphology
|
J:89391
|
abnormal sperm connecting piece morphology
|
J:89391
|
abnormal sperm nucleus morphology
|
J:102121,
J:72756,
J:89391
|
absent acrosome
|
J:72756
|
absent sperm mitochondrial sheath
|
J:72756
|
asthenozoospermia
|
J:102121,
J:72756
|
ectopic manchette
|
J:89391
|
elongated manchette
|
J:89391
|
enlarged sperm head
|
J:102121
|
globozoospermia
|
J:72756
|
multiflagellated sperm
|
J:102121
|
oligozoospermia
|
J:72756
|
teratozoospermia
|
J:102121,
J:72756
|
Aggf1Gt(PT036)Byg/Aggf1+
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased lung endothelial cell migration
|
J:239252
|
Ago2Gt(XE344)Byg/Ago2Gt(XE344)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:121791
|
Ago2tm1.1Tara/Ago2tm1.1Tara Tg(Ins2-cre)23Herr/0
(involves: 129P2/OlaHsd * C57BL/6J * CBA/J)
|
decreased pancreatic beta cell proliferation
|
J:210552
|
Ago4tm1.1Peco/Ago4tm1.1Peco
(B6.129P2(FVB)-Ago4tm1.1Peco)
|
abnormal male germ cell morphology
|
J:187588
|
abnormal male meiosis
|
J:187588
|
abnormal synaptonemal complex
|
J:187588
|
increased male germ cell apoptosis
|
J:187588
|
oligozoospermia
|
J:187588
|
Agpat1tm1Garg/Agpat1tm1Garg
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal spermatocyte morphology
|
J:250301
|
arrest of male meiosis
|
J:250301
|
decreased elongated spermatid number
|
J:250301
|
decreased round spermatid number
|
J:250301
|
decreased spermatid number
|
J:250301
|
Agpat3tm1a(EUCOMM)Wtsi/Agpat3tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal sperm head morphology
|
J:245638
|
oligozoospermia
|
J:245638
|
teratozoospermia
|
J:245638
|
Agpsbs2/Agpsbs2
(STOCK Agpsbs2/J)
|
azoospermia
|
J:171265
|
Agr2tm1.1Lex/Agr2tm1.1Lex
(involves: 129S5/SvEvBrd * BALB/cJ * C57BL/6)
|
increased cell proliferation
|
J:195573
|
Agr2tm1.1Lpkn/Agr2tm1.1Lpkn Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129 * 129S6/SvEvTac * C57BL/6)
|
abnormal enterocyte proliferation
|
J:156704
|
abnormal intestinal goblet cell morphology
|
J:156704
|
increased enterocyte apoptosis
|
J:156704
|
Agr2tm1.2Lpkn/Agr2tm1.2Lpkn
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:156704
|
Agr2tm1Lex/Agr2tm1Lex Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * 129S5/SvEvBrd * C57BL/6)
|
increased cell proliferation
|
J:195573
|
Agtpbp1atms/Agtpbp1atms Faslpr/?
(MRL/Mp-Agtpbp1atms Faslpr)
|
oligozoospermia
|
J:103945
|
Agtpbp1m2Btlr/Agtpbp1m2Btlr
(C57BL/6J-Agtpbp1m2Btlr)
|
decreased activated sperm motility
|
J:159361
|
Agtpbp1pcd-3J/Agtpbp1pcd-3J
(involves: BALB/cByJ)
|
abnormal male germ cell morphology
|
J:74929
|
asthenozoospermia
|
J:74929
|
oligozoospermia
|
J:74929
|
Agtpbp1pcd-6J/Agtpbp1pcd-6J
(C57BL/6J-Agtpbp1pcd-6J/J)
|
azoospermia
|
J:87349
|
Agtpbp1pcd-8J/Agtpbp1pcd-8J
(BALB/cJ-Agtpbp1pcd-8J/GrsrJ)
|
abnormal male germ cell morphology
|
J:132487
|
Agtpbp1pcd-Btlr/Agtpbp1pcd-Btlr
(C57BL/6J-Agtpbp1pcd-Btlr)
|
oligozoospermia
|
J:133627
|
teratozoospermia
|
J:133627
|
Agtpbp1pcd-Tg(Dhfr)1Jwg/Agtpbp1pcd-Tg(Dhfr)1Jwg
(involves: C57BL/6J * CD-1 * DBA/2J)
|
azoospermia
|
J:9814
|
Agtpbp1pcd/Agtpbp1pcd
(involves: C57BR/cdJ * CBA)
|
abnormal male germ cell morphology
|
J:5613
|
asthenozoospermia
|
J:5613
|
oligozoospermia
|
J:5613
|
Agtpbp1pcd/Agtpbp1pcd
(B6.BR-Agtpbp1pcd/J)
|
abnormal photoreceptor connecting cilium morphology
|
J:249732
|
Agtr1atm1Ecl/Agtr1atm1Ecl
(involves: 129S2/SvPas * C57BL/6)
|
cardiac interstitial fibrosis
|
J:124206
|
Agtr2tm1Tin/Y
(involves: 129P2/OlaHsd)
|
decreased kidney apoptosis
|
J:48005
|
Ahctf1tm1Taga/Ahctf1tm1Taga
(involves: C57BL/6 * CBA)
|
abnormal inner cell mass apoptosis
|
J:98254
|
absent inner cell mass proliferation
|
J:98254
|
Ahcyem1Cya/Ahcy+
(C57BL/6N-Ahcyem1Cya/Cya)
|
oxidative stress
|
J:298071
|
Ahi1tm1Jgg/Ahi1tm1Jgg
(involves: 129 * C57BL/6 * FVB/N)
|
abnormal retina apoptosis
|
J:158019
|
Ahi1tm1Jgg/Ahi1tm1Jgg Tg(TCF/Lef1-lacZ)34Efu/0
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal basement membrane morphology
|
J:154321
|
Ahi1tm1Rujf/Ahi1tm1Rujf
(C57BL/6-Ahi1tm1Rujf)
|
abnormal cilium morphology
|
J:152919
|
Ahnaktm1Vtm/Ahnaktm1Vtm
(involves: 129S1/Sv * C57BL/6)
|
decreased T cell proliferation
|
J:131148
|
Ahrb-1/Ahrb-1 Aiptm2.1Bra/Aiptm2.1Bra Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(B6.Cg-Speer6-ps1Tg(Alb-cre)21Mgn Aiptm2.1Bra)
|
patent ductus venosus
|
J:166864
|
Ahrtm1.2Arte/Ahrtm1.2Arte
(involves: C57BL/6NTac)
|
abnormal male germ cell apoptosis
|
J:210360
|
abnormal sperm head morphology
|
J:210360
|
coiled sperm flagellum
|
J:210360
|
multinucleated giant male germ cells
|
J:210360
|
teratozoospermia
|
J:210360
|
Ahrtm1Bra/Ahrtm1Bra
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
patent ductus venosus
|
J:83597
|
Ahrtm1Bra/Ahrtm1Bra
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased germ cell number
|
J:83527
|
patent ductus venosus
|
J:166864,
J:94465
|
Ahrtm1Bra/Ahrtm1Bra
(B6.129-Ahrtm1Bra)
|
patent ductus venosus
|
J:64483
|
Ahrtm2Bra/Ahrtm2Bra
(involves: 129/Sv * C57BL/6)
|
patent ductus venosus
|
J:83597
|
Ahrtm3.1Bra/Ahrtm3.1Bra Tg(Six3-cre)69Frty/0
(Not Specified)
|
increased retina apoptosis
|
J:265123
|
Ahrtm3.1Bra/Ahrtm3.1Bra Tg(Tek-cre)12Flv/0
(B6.Cg-Ahrtm3.1Bra Tg(Tek-cre)12Flv)
|
patent ductus venosus
|
J:104388
|
Ahrtm3Bra/Ahrtm3Bra
(involves: 129/Sv * C57BL/6J * DBA/2)
|
patent ductus venosus
|
J:94465
|
Ahrtm4.1Bra/Ahrtm4.1Bra
(involves: 129/Sv * C57BL/6)
|
patent ductus venosus
|
J:141978
|
Ahsptm1.1Mjwe/Ahsptm1.1Mjwe
(involves: 129S6/SvEvTac * C57BL/6)
|
increased cellular sensitivity to oxidative stress
|
J:94421
|
oxidative stress
|
J:94421
|
Ahsptm1Mjwe/Ahsptm1Mjwe
(involves: 129S6/SvEvTac * C57BL/6)
|
increased cellular sensitivity to oxidative stress
|
J:94421
|
oxidative stress
|
J:94421
|
Aicdatm1(cre)Mnz/Aicda+ Ightm3Mnz/Igh+ Myctm37Mnz/Myc+
(involves: 129P2/OlaHsd * C57BL/6)
|
spontaneous chromosome breakage
|
J:145691
|
Aicdatm1(cre)Mnz/Aicda+ Ightm3Mnz/Igh+ Myctm39Mnz/Myc+
(involves: 129P2/OlaHsd * C57BL/6)
|
spontaneous chromosome breakage
|
J:145691
|
Aicdatm1Hon/Aicdatm1Hon Ightm3Mnz/Igh+ Myctm37Mnz/Myc+
(involves: C57BL/6 * CBA)
|
induced chromosome breakage
|
J:145691
|
Aicdatm1Hon/Aicdatm1Hon Tg(Cr2-cre)3Cgn/? Xrcc4tm1Fwa/Xrcc4tm2Fwa
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * CBA)
|
spontaneous chromosome breakage
|
J:150339
|
Aicdatm1Hon/Aicdatm2Mnz
(involves: C57BL/6 * CBA)
|
chromosomal instability
|
J:136224
|
Aicdatm2Mnz/Aicdatm2Mnz
(B6.Cg-Aicdatm2Mnz)
|
chromosomal instability
|
J:136224
|
Aifm1Hq/Y
(B6CBACa Aw-J/A-Aifm1Hq/J)
|
abnormal cell cycle
|
J:78983
|
abnormal respiratory electron transport chain
|
J:144096
|
decreased susceptibility to neuronal excitotoxicity
|
J:98103
|
increased cardiomyocyte apoptosis
|
J:110278
|
increased cellular sensitivity to hydrogen peroxide
|
J:78983
|
oxidative stress
|
J:78983,
J:110278
|
Aifm1Hq/Aifm1Hq
(B6CBACa Aw-J/A-Aifm1Hq/J)
|
abnormal cell cycle
|
J:78983
|
abnormal respiratory electron transport chain
|
J:144096
|
decreased susceptibility to neuronal excitotoxicity
|
J:98103
|
increased cardiomyocyte apoptosis
|
J:110278
|
increased cellular sensitivity to hydrogen peroxide
|
J:78983
|
oxidative stress
|
J:78983,
J:110278
|
Aifm1Hq/Aifm1Hq Apaf1Gt(IRESBetageo)XIX18Pgr/Apaf1Gt(IRESBetageo)XIX18Pgr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased neuron apoptosis
|
J:98103
|
Aifm1tm1Pngr/Y
(129P2/OlaHsd-Aifm1tm1Pngr)
|
abnormal cell physiology
|
J:68434
|
Aifm1tm2.1Pngr/Y
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal respiratory electron transport chain
|
J:111066
|
increased embryonic tissue cell apoptosis
|
J:111066
|
Aifm1tm2.1Pngr/Aifm1tm2.1Pngr
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal respiratory electron transport chain
|
J:111066
|
increased embryonic tissue cell apoptosis
|
J:111066
|
Aifm1tm2Pngr/Y Foxg1tm1(cre)Skm/Foxg1+
(involves: 129P2/OlaHsd)
|
abnormal mitochondrial morphology
|
J:112874
|
abnormal mitochondrial physiology
|
J:112874
|
decreased mitochondrial fission
|
J:112874
|
decreased neuron apoptosis
|
J:112874
|
increased neuron apoptosis
|
J:112874
|
Aifm1tm2Pngr/Y Tg(Ckmm-cre)5Khn/0
(involves: 129P2/OlaHsd * FVB)
|
abnormal aerobic respiration
|
J:113016
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:113016
|
abnormal mitochondrial crista morphology
|
J:113016
|
abnormal mitochondrial morphology
|
J:113016
|
abnormal mitochondrial physiology
|
J:113016
|
abnormal respiratory electron transport chain
|
J:113016
|
increased mitochondrial number
|
J:113016
|
oxidative stress
|
J:113016
|
Aifm2tm1Hbsh/Aifm2tm1Hbsh
(involves: 129S6/SvEvTac)
|
abnormal cell proliferation
|
J:105660
|
Aim2Gt(CSG445)Byg/Aim2Gt(CSG445)Byg
(B6.129P2-Aim2Gt(CSG445)Byg/J)
|
decreased macrophage apoptosis
|
J:234263
|
Aiptm1Bra/Aip+
(Not Specified)
|
patent ductus venosus
|
J:167350
|
Aiptm2Bra/Aip+
(involves: 129)
|
patent ductus venosus
|
J:167350
|
Aiptm2Bra/Aiptm2Bra
(involves: 129)
|
patent ductus venosus
|
J:167350
|
Airetm1Pltn/Airetm1Pltn
(involves: 129S4/SvJae * C57BL/6)
|
increased T cell proliferation
|
J:77873
|
Airntm1Dpb/Airn+
(involves: FVB/N)
|
maternal imprinting
|
J:77594
|
Airntm1Dpb/Airntm1Dpb
(involves: FVB/N)
|
maternal imprinting
|
J:77594
|
Airntm2.1Dpb/Airntm2.1Dpb
(involves: 129S2/SvPas * 129S4/SvJaeSor * FVB/N)
|
abnormal DNA methylation
|
J:183397
|
maternal effect
|
J:183397
|
Ajubatm1Gdl/Ajubatm1Gdl
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell migration
|
J:98248
|
Ak1tm1Bew/Ak1tm1Bew
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal tricarboxylic acid cycle
|
J:66101
|
Ak1tm1Bew/Ak1tm1Bew Ckmtm1Bew/Ckmtm1Bew
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6)
|
abnormal aerobic respiration
|
J:109659
|
Ak2Gt(OST495245)Lex/Ak2Gt(OST495245)Lex
(involves: 129S5/SvEvBrd * C57BL/6N)
|
abnormal mitochondrial morphology
|
J:305579
|
disorganized mitochondrial cristae
|
J:305579
|
Ak6tm1.1Zhexf/Ak6+
(involves: C57BL/6)
|
abnormal ribosome biogenesis
|
J:241160
|
abnormal translation
|
J:241160
|
Ak7Gt(OST434404)Lex/Ak7Gt(OST434404)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
oligozoospermia
|
J:185566
|
Ak7Tg(tetO-Hmox1)67Sami/Ak7Tg(tetO-Hmox1)67Sami
(FVB/N-Ak7Tg(tetO-Hmox1)67Sami)
|
abnormal respiratory motile cilium morphology
|
J:186062
|
abnormal respiratory motile cilium physiology
|
J:186062
|
abnormal sperm head morphology
|
J:186062
|
azoospermia
|
J:186062
|
Ak9em1Lnl/Ak9em1Lnl
(C57BL/6J-Ak9em1Lnl)
|
asthenozoospermia
|
J:340782
|
Ak9em1Mdj/Ak9+
(C57BL/6-Ak9em1Mdj)
|
abnormal brain ependyma motile cilium physiology
|
J:344356
|
Ak9em1Mdj/Ak9em1Mdj
(C57BL/6-Ak9em1Mdj)
|
abnormal brain ependyma motile cilium morphology
|
J:344356
|
abnormal brain ependyma motile cilium physiology
|
J:344356
|
abnormal sperm motility
|
J:344356
|
decreased brain ependyma motile cilium length
|
J:344356
|
Akap1tm1Gsm/Akap1tm1Gsm
(B6.Cg-Akap1tm1Gsm)
|
abnormal female meiosis
|
J:106320
|
Akap3em1Hqi/Akap3em1Hqi
(Not Specified)
|
abnormal sperm flagellum morphology
|
J:284173
|
abnormal sperm principal piece morphology
|
J:284173
|
coiled sperm flagellum
|
J:284173
|
decreased hyperactivated sperm motility
|
J:284173
|
short sperm flagellum
|
J:284173
|
Akap4em1Bbw/Y
(C57BL/6J-Akap4em1Bbw)
|
abnormal sperm fibrous sheath morphology
|
J:352416
|
abnormal sperm principal piece morphology
|
J:352416
|
decreased sperm progressive motility
|
J:352416
|
kinked sperm flagellum
|
J:352416
|
oligozoospermia
|
J:352416
|
short sperm flagellum
|
J:352416
|
Akap4em1Hqi/Y
(Not Specified)
|
abnormal sperm flagellum morphology
|
J:284173
|
abnormal sperm principal piece morphology
|
J:284173
|
coiled sperm flagellum
|
J:284173
|
decreased hyperactivated sperm motility
|
J:284173
|
short sperm flagellum
|
J:284173
|
Akap4tm1Eddy/Y
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal sperm end piece morphology
|
J:86899
|
abnormal sperm flagellum morphology
|
J:86899
|
abnormal sperm mitochondrial sheath morphology
|
J:86899
|
abnormal sperm principal piece morphology
|
J:86899
|
coiled sperm flagellum
|
J:86899
|
decreased activated sperm motility
|
J:86899
|
decreased hyperactivated sperm motility
|
J:86899
|
decreased sperm mitochondrial sheath size
|
J:86899
|
short sperm flagellum
|
J:86899
|
Akap6tm1.1Mskf/Akap6tm1.1Mskf A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: C57BL/6 * FVB/N * SJL)
|
cardiac interstitial fibrosis
|
J:214288
|
increased cardiomyocyte apoptosis
|
J:214288
|
Akap9mei2-5/Akap9mei2-5
(involves: 129S1/Sv * C57BL/6)
|
arrest of male meiosis
|
J:86161
|
Akap9mei2-5/Akap9mei2-5
(involves: 129S1/Sv)
|
abnormal spermatocyte morphology
|
J:198499
|
azoospermia
|
J:198499
|
Akap9mei2-5/Akap9repro12
(involves: 129S1/Sv * C57BL/6J)
|
azoospermia
|
J:198499
|
Akap9repro12/Akap9repro12
(involves: C3HeB/FeJ * C57BL/6J)
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
Akap9repro12/Akap9tm1b(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N * FVB/N)
|
azoospermia
|
J:198499
|
Akap13Gt(CSJ306)Byg/Akap13Gt(CSJ306)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
cardiac interstitial fibrosis
|
J:231257
|
Akr1a1Gt(OST222400)Lex/Akr1a1Gt(OST222400)Lex
(B6.129S5-Akr1a1Gt(OST222400)Lex)
|
abnormal osteoblast differentiation
|
J:164548
|
abnormal osteoblast physiology
|
J:164548
|
Akr1b8tm1Dgen/Akr1b8tm1Dgen
(Not Specified)
|
oxidative stress
|
J:301852
|
Akr1c21em1Wany/Akr1c21em1Wany
(involves: C57BL/6)
|
oxidative stress
|
J:322353
|
Akt1tm1Nhy/Akt1tm1Nhy
(involves: 129/Sv * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:71404
|
multinucleated giant male germ cells
|
J:71404
|
oligozoospermia
|
J:71404
|
Akt1tm1Pnt/Akt1tm1Pnt Akt2tm1.1Mbb/Akt2tm1.1Mbb Akt3tm1Mbb/Akt3tm1Mbb Tg(Lck-cre)1Cwi/0
(involves: 129P2/OlaHsd)
|
increased T cell apoptosis
|
J:135903
|
Akt1tm1Pnt/Akt1tm1Pnt Akt2tm1.1Mbb/Akt2tm1.1Mbb Tg(Lck-cre)1Cwi/0
(involves: 129P2/OlaHsd)
|
increased T cell apoptosis
|
J:135903
|
Akt1tm2.1Mbb/Akt1tm2.1Mbb
(involves: 129S4/SvJae * C57BL/6J * FVB/N)
|
increased fatty acid oxidation
|
J:182721
|
Akt2tm1.1Mbb/Akt2tm1.1Mbb
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased adipocyte glucose uptake
|
J:71491
|
decreased skeletal muscle cell glucose uptake
|
J:71491
|
Akt3tm1Hem/Akt3tm1Hem
(involves: 129P2/OlaHsd * C57BL/6)
|
increased susceptibility to neuronal excitotoxicity
|
J:98804
|
Aktiptm1a(EUCOMM)Hmgu/Aktiptm1a(EUCOMM)Hmgu
(C57BL/6N-Aktiptm1a(EUCOMM)Hmgu)
|
decreased fibroblast proliferation
|
J:276210
|
increased cellular sensitivity to DNA damaging agents
|
J:276210
|
increased cellular sensitivity to hydroxyurea
|
J:276210
|
Aktiptm1a(EUCOMM)Hmgu/Aktiptm1a(EUCOMM)Hmgu Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas * C57BL/6N)
|
cellular phenotype
|
J:276210
|
increased fibroblast proliferation
|
J:276210
|
Albtm1(cre/ERT2)Mtz/Alb+ Polr2mtm1.1Rgr/Polr2mtm1.1Rgr Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
increased hepatocyte karyomegaly
|
J:291184
|
increased hepatocyte proliferation
|
J:291184
|
Albtm1(cre/ERT2)Mtz/Albtm1(cre/ERT2)Mtz Slc2a2tm2Thor/Slc2a2tm2Thor
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6)
|
decreased cellular glucose uptake
|
J:197607
|
increased skeletal muscle cell glucose uptake
|
J:197607
|
Aldh1a1tm1.1Ngb/Aldh1a1tm1.1Ngb Aldh1a3tm1.1Pcn/Aldh1a3tm1.1Pcn
(involves: 129/Sv * C57BL/6 * SJL)
|
decreased periocular mesenchyme apoptosis
|
J:102847
|
Aldh1a1tm1Gdu/Aldh1a1tm1Gdu Aldh1a2tm1.1Mbp/Aldh1a2tm1.1Mbp Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
azoospermia
|
J:324715
|
Aldh1a1tm1Gdu/Aldh1a1tm1Gdu Aldh1a2tm1.1Mbp/Aldh1a2tm1.2Mbp Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: 129 * C57BL/6 * SJL)
|
azoospermia
|
J:324715
|
Aldh1a1tm1Gdu/Aldh1a1tm1Gdu Aldh1a3tm1Gdu/Aldh1a3tm1Gdu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased periocular mesenchyme apoptosis
|
J:108515
|
Aldh1a2tm1Dll/Aldh1a2tm1Ipc
(involves: CD-1)
|
abnormal neural crest cell migration
|
J:81969
|
Aldh1a3tm1.1Pcn/Aldh1a3tm1.1Pcn
(involves: 129/Sv * C57BL/6)
|
decreased periocular mesenchyme apoptosis
|
J:102847
|
Aldh1b1tm1.1(KOMP)Vlcg/Aldh1b1tm1.1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac * CBA)
|
abnormal pancreatic beta cell differentiation
|
J:232360
|
increased pancreatic beta cell apoptosis
|
J:232360
|
increased pancreatic beta cell proliferation
|
J:232360
|
increased pancreatic islet cell apoptosis
|
J:232360
|
oxidative stress
|
J:232360
|
Aldh1l2tm2e(KOMP)Wtsi/Aldh1l2tm2e(KOMP)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
abnormal cell physiology
|
J:299012
|
decreased fatty acid beta-oxidation
|
J:299012
|
Aldh2tm1.1Mak/Aldh2+
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased hepatocyte apoptosis
|
J:223796
|
Aldh2tm1.1Mak/Aldh2tm1.1Mak
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased hepatocyte apoptosis
|
J:223796
|
Aldh2tm1a(EUCOMM)Wtsi/Aldh2tm1a(EUCOMM)Wtsi Fancd2tm1Hou/Fancd2+
(involves: 129S4/SvJae * C57BL/6J * C57BL/6N)
|
maternal effect
|
J:193232
|
Aldh2tm1a(EUCOMM)Wtsi/Aldh2tm1a(EUCOMM)Wtsi Fancd2tm1Hou/Fancd2tm1Hou
(involves: 129S4/SvJae * C57BL/6J * C57BL/6N)
|
increased sensitivity to induced cell death
|
J:188123
|
Aldh2tm1Kaw/Aldh2tm1Kaw
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cellular respiration
|
J:63498
|
Aldh3a2tm1b(EUCOMM)Wtsi/Aldh3a2tm1b(EUCOMM)Wtsi
(involves: C57BL * C57BL/6J * C57BL/6N * DBA)
|
increased keratinocyte proliferation
|
J:234695
|
oxidative stress
|
J:234695
|
Aldh7a1tm1d(EUCOMM)Hmgu/Aldh7a1tm1d(EUCOMM)Hmgu
(B6(FVB)-Aldh7a1tm1d(EUCOMM)Hmgu)
|
oxidative stress
|
J:298561
|
Alg2tm1Lex/Alg2+
(B6;129S5-Alg2tm1Lex/Mmucd)
|
decreased dermal fibroblast proliferation
|
J:171883
|
Alktm1.1Rhp/Alktm1.1Rhp
(involves: 129 * C57BL/6N)
|
abnormal male germ cell morphology
|
J:226955
|
increased testis apoptosis
|
J:226955
|
Alkbh1tm1Klng/Alkbh1tm1Klng
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:200274
|
decreased male germ cell number
|
J:166841
|
Alkbh2tm1Klng/Alkbh2tm1Klng
(involves: C57BL/6J)
|
abnormal DNA repair
|
J:108782
|
Alkbh2tm1Klng/Alkbh2tm1Klng Alkbh3tm1Klng/Alkbh3tm1Klng
(involves: C57BL/6J)
|
abnormal DNA repair
|
J:108782
|
Alkbh4tm1Geno/Alkbh4tm1Geno Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
abnormal centrosome morphology
|
J:205739
|
abnormal mitotic cytokinesis
|
J:205739
|
decreased fibroblast cell migration
|
J:205739
|
increased cell nucleus count
|
J:205739
|
Alkbh5tm1.1Klng/Alkbh5tm1.1Klng
(Not Specified)
|
abnormal male germ cell apoptosis
|
J:194218
|
oligozoospermia
|
J:194218
|
teratozoospermia
|
J:194218
|
Alkbh7tm1.1Klng/Alkbh7tm1.1Klng
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal aerobic respiration
|
J:198968
|
abnormal fatty acid oxidation
|
J:198968
|
abnormal mitochondrial physiology
|
J:198968
|
decreased cellular sensitivity to alkylating agents
|
J:299035
|
decreased cellular sensitivity to hydrogen peroxide
|
J:299035
|
decreased cellular sensitivity to methylmethanesulfonate
|
J:299035
|
decreased sensitivity to induced cell death
|
J:299035
|
Alms1Gt(XH152)Byg/Alms1Gt(XH152)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
cellular phenotype
|
J:100403
|
Alms1L2131X/Alms1L2131X
(involves: C57BL/6 * NOD)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:118221
|
increased kidney apoptosis
|
J:118221
|
increased kidney cell proliferation
|
J:118221
|
Alox5tm1Bhk/Alox5tm1Bhk
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * DBA/2))
|
impaired neutrophil chemotaxis
|
J:68714
|
Alox15tm1.1Nadl/Alox15tm1.1Nadl Tg(Pdx1-cre)89.1Dam/0
(involves: C57BL/6 * CBA)
|
abnormal redox activity
|
J:224344
|
Alpltm1(cre)Nagy/Alpl+ Atg7tm1Tchi/Atg7tm1Tchi
(involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal acrosome assembly
|
J:258511
|
abnormal acrosome morphology
|
J:258511
|
abnormal proacrosomal vesicle fusion
|
J:258511
|
abnormal sperm nucleus morphology
|
J:258511
|
globozoospermia
|
J:258511
|
impaired autophagy
|
J:258511
|
increased male germ cell apoptosis
|
J:258511
|
oligozoospermia
|
J:258511
|
Alpltm1(cre)Nagy/Alpl+ Dicer1tm1.1Mnn/Dicer1tm1.2Mnn
(involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6J)
|
abnormal meiotic spindle morphology
|
J:150221
|
abnormal oocyte morphology
|
J:150221
|
Alpltm1(cre)Nagy/Alpl+ Dmrt1tm1Zark/Dmrt1tm1.1Zark
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal spermatogonia morphology
|
J:122954
|
decreased male germ cell number
|
J:122954
|
Alpltm1(cre)Nagy/Alpl+ Dnmt3atm3.1Enl/Dnmt3atm3.2Enl
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
azoospermia
|
J:91108
|
Alpltm1(cre)Nagy/Alpl+ Ehmt2tm2Yshk/Ehmt2tm2.1Yshk
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal female meiosis
|
J:123269
|
arrest of male meiosis
|
J:123269
|
azoospermia
|
J:123269
|
decreased male germ cell number
|
J:123269
|
decreased oocyte number
|
J:123269
|
Alpltm1(cre)Nagy/Alpl+ Pknox1tm1.1Rygo/Pknox1tm1.1Rygo
(involves: 129 * C57BL/6 * C57BL/6JJcl)
|
abnormal spermatogonia morphology
|
J:258387
|
abnormal spermatogonia proliferation
|
J:258387
|
azoospermia
|
J:258387
|
decreased male germ cell number
|
J:258387
|
increased male germ cell apoptosis
|
J:258387
|
Alpltm1(cre)Nagy/Alpl+ Pou5f1tm1Scho/Pou5f1tm1.1Scho
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased primordial germ cell number
|
J:95317
|
oligozoospermia
|
J:95317
|
Alpltm1(cre)Nagy/Alpl+ Tet3tm1.1Gxu/Tet3tm1.2Gxu
(involves: 129 * C57BL/6J * SJL)
|
abnormal DNA methylation
|
J:176196
|
maternal effect
|
J:176196
|
Alpltm1(cre)Nagy/Alpl+ Xrcc1tm1Pmc/Xrcc1tm1Pmc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:292217
|
abnormal mitochondrial morphology
|
J:292217
|
abnormal mitochondrial physiology
|
J:292217
|
abnormal spermatocyte morphology
|
J:292217
|
abnormal spermatogonia morphology
|
J:292217
|
asthenozoospermia
|
J:292217
|
increased testis apoptosis
|
J:292217
|
oligozoospermia
|
J:292217
|
oxidative stress
|
J:292217
|
Alpltm1Jlm/Alpltm1Jlm
(involves: 129S2/SvPas * C57BL/6)
|
abnormal osteoblast physiology
|
J:128077
|
Alpltm1Jlm/Alpltm1Jlm Spp1tm1Rit/Spp1tm1Rit
(involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6)
|
abnormal osteoblast physiology
|
J:128077
|
Altretm1.1Hbgl/Altretm1.1Hbgl Foxp3tm4(YFP/icre)Ayr/Y
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:342907
|
abnormal mitochondrial physiology
|
J:342907
|
decreased mitochondrial size
|
J:342907
|
increased regulatory T cell apoptosis
|
J:342907
|
Alx1em1Jian/Alx1em1Jian
(C57BL/6N-Alx1em1Jian)
|
increased periocular mesenchyme apoptosis
|
J:320497
|
Alx3tm1Hubr/Alx3tm1Hubr
(involves: 129P2/OlaHsd)
|
increased pancreatic beta cell apoptosis
|
J:166436
|
Alx3tm1Hubr/Alx3tm1Hubr
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
abnormal cell death
|
J:163651
|
am/am
(involves: 101 * C3H)
|
abnormal cell adhesion
|
J:6007
|
am/am
(involves: 101 * CBA)
|
abnormal cell adhesion
|
J:6105,
J:6435
|
Ambptm1Kkm/Ambptm1Kkm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal oocyte morphology
|
J:68027
|
Ambptm1Miya/Ambptm1Miya
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal oocyte morphology
|
J:68118
|
absent zona pellucida
|
J:68118
|
Ambra1Gt(pGT1.8geo)1Fcec/Ambra1Gt(pGT1.8geo)1Fcec
(involves: C57BL/6)
|
impaired autophagy
|
J:122795
|
increased cell proliferation
|
J:122795
|
increased embryonic neuroepithelium apoptosis
|
J:122795
|
Amer1tm1.1Nbar/Y Tg(Prrx1-cre)1Cjt/0
(involves: 129S4/SvJae * C57BL/6 * SJL)
|
abnormal fat cell differentiation
|
J:173242
|
abnormal osteoblast differentiation
|
J:173242
|
Amer1tm1.2Nbar/Y
(involves: 129S4/SvJae * C57BL/6 * CD-1 * SJL)
|
increased metanephric mesenchyme apoptosis
|
J:173242
|
Amfrtm1.1Amw/Amfrtm1.1Amw
(B6.129-Amfrtm1.1Amw)
|
cellular phenotype
|
J:200251
|
Amhr2tm3(cre)Bhr/Amhr2+ Artm1Chc/Y
(involves: 129S/SvEv * C57BL/6)
|
abnormal meiosis
|
J:118270
|
arrest of male meiosis
|
J:118270
|
azoospermia
|
J:118270
|
Amhr2tm3(cre)Bhr/Amhr2+ Nr5a1tm1Klp/Nr5a1tm2Klp
(involves: 129P2/OlaHsd * 129S7/SvEvBrd)
|
decreased granulosa cell proliferation
|
J:145805
|
Amhr2tm3(cre)Bhr/Amhr2+ Smad2tm1Cxd/Smad2tm1.1Mwst Smad3tm1Par/Smad3tm1Zuk
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased oocyte number
|
J:142827
|
Amhr2tm3(cre)Bhr/Amhr2+ Smad4tm1Rob/Smad4tm1.1Rob
(involves: 129S/SvEv * C57BL/6J)
|
decreased oocyte number
|
J:108954
|
Amhr2tm3(cre)Bhr/Amhr2+ Stk11tm1Rdp/Stk11tm1Rdp
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6)
|
decreased male germ cell number
|
J:187754
|
increased Sertoli cell proliferation
|
J:187754
|
Amhr2tm3(cre)Bhr/Amhr2+ Tsc1tm1Djk/Tsc1tm1Djk
(involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6)
|
abnormal oocyte morphology
|
J:181774
|
decreased male germ cell number
|
J:187754
|
increased Sertoli cell proliferation
|
J:187754
|
oocyte degeneration
|
J:181774
|
Amhr2tm3(cre)Bhr/Amhr2+ Tsc2tm1.1Mjg/Tsc2tm1.1Mjg
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6)
|
decreased male germ cell number
|
J:187754
|
increased Sertoli cell proliferation
|
J:187754
|
Amnamn/Amnamn
(involves: C57BL/6J)
|
increased embryonic tissue cell apoptosis
|
J:50810
|
Amottm1Bhr/Y
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal anterior visceral endoderm cell migration
|
J:82844
|
Amottm1Bhr/Amottm1Bhr
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal anterior visceral endoderm cell migration
|
J:82844
|
Amphtm1Pdc/Amphtm1Pdc
(involves: 129/Sv * C57BL/6)
|
decreased spermatid number
|
J:141046
|
Anapc2tm1Kna/Anapc2tm1Kna Tg(Ttr-cre/Esr1*)1Vco/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
increased hepatocyte proliferation
|
J:87782
|
Anapc2tm1Kna/Anapc2tm2Kna Tg(Mx1-cre)1Cgn/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
increased hepatocyte proliferation
|
J:87782
|
Angtm1Dats/Angtm1Dats
(Not Specified)
|
increased cellular sensitivity to gamma-irradiation
|
J:236081
|
increased hematopoietic stem cell proliferation
|
J:236081
|
Angel2em1Gpt/Angel2em1Gpt
(C57BL/6N-Angel2em1Gpt)
|
abnormal oxidative phosphorylation
|
J:332461
|
abnormal respiratory electron transport chain
|
J:332461
|
abnormal translation
|
J:332461
|
Angpt2tm1Gdy/Angpt2tm1Gdy
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal vascular regression
|
J:89618
|
Angptl2tm1Yo/Angptl2tm1Yo
(B6.Cg-Angptl2tm1Yo)
|
impaired macrophage chemotaxis
|
J:152387
|
Ank2tm1Bnt/Ank2+
(involves: 129)
|
abnormal fat cell differentiation
|
J:222913
|
decreased adipocyte glucose uptake
|
J:222913
|
Ank2tm2.1Bnt/Ank2tm2.1Bnt
(STOCK Ank2tm2Bnt/J)
|
abnormal fat cell differentiation
|
J:222913
|
increased adipocyte glucose uptake
|
J:222913
|
Ank2tm3.1Bnt/Ank2tm3.1Bnt
(B6.129(C)-Ank2tm3.1Bnt/J)
|
abnormal fat cell differentiation
|
J:222913
|
decreased adipocyte glucose uptake
|
J:222913
|
decreased skeletal muscle cell glucose uptake
|
J:222913
|
increased adipocyte glucose uptake
|
J:222913
|
increased skeletal muscle cell glucose uptake
|
J:222913
|
Ankank/Ankank
(involves: BALB/c * C3H * C57BL/6 * JGBF/Le)
|
abnormal osteoblast physiology
|
J:111462
|
Anktm1.1Ejr/Ank+
(B6.129-Anktm1.1Ejr)
|
abnormal osteoclast differentiation
|
J:168526
|
Anktm1.1Ejr/Anktm1.1Ejr
(B6.129-Anktm1.1Ejr)
|
abnormal osteoclast differentiation
|
J:168526
|
Ankfy1Gt(RRE069)Byg/Ankfy1+
(B6.129P2-Ankfy1Gt(RRE069)Byg)
|
increased brain apoptosis
|
J:250135
|
Ankle1tm1.2(KOMP)Wtsi/Ankle1tm1.2(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
cellular phenotype
|
J:235782
|
Ankmy2tm1b(EUCOMM)Hmgu/Ankmy2tm1b(EUCOMM)Hmgu Ift88tm1Bky/Ift88tm1Bky
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N)
|
absent embryonic cilia
|
J:297055
|
Ankrd31em1Atot/Ankrd31em1Atot
(involves: C57BL/6J)
|
abnormal chromosomal synapsis
|
J:276412
|
abnormal double-strand DNA break repair
|
J:276412
|
abnormal female meiosis
|
J:276412
|
abnormal male meiosis
|
J:276412
|
abnormal meiosis
|
J:276412
|
abnormal spermatocyte morphology
|
J:276412
|
abnormal synaptonemal complex
|
J:276412
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:276412
|
absent chiasmata formation
|
J:276412
|
arrest of male meiosis
|
J:276412
|
decreased oocyte number
|
J:276412
|
increased female germ cell apoptosis
|
J:276412
|
increased male germ cell apoptosis
|
J:276412
|
Ankrd31em1Flor/Ankrd31em1Flor
(C57BL/6JCrl-Ankrd31em1Flor)
|
abnormal male meiosis
|
J:314966
|
abnormal sperm head morphology
|
J:314966
|
abnormal sperm nucleus morphology
|
J:314966
|
asthenozoospermia
|
J:314966
|
decreased sperm progressive motility
|
J:314966
|
oligozoospermia
|
J:314966
|
Ankrd31em1Sky/Ankrd31em1Sky
(involves: C57BL/6J * CBA/J)
|
abnormal chromosomal synapsis
|
J:276385
|
abnormal double-strand DNA break repair
|
J:276385
|
abnormal male meiosis
|
J:276385
|
abnormal oogenesis
|
J:276385
|
abnormal spermatocyte morphology
|
J:276385
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:276385
|
absent chiasmata formation
|
J:276385
|
arrest of male meiosis
|
J:276385
|
azoospermia
|
J:276385
|
decreased oocyte number
|
J:276385
|
increased male germ cell apoptosis
|
J:276385
|
Ankrd31em2Flor/Ankrd31em2Flor
(C57BL/6JCrl-Ankrd31em2Flor)
|
abnormal male meiosis
|
J:314966
|
abnormal sperm head morphology
|
J:314966
|
abnormal sperm nucleus morphology
|
J:314966
|
asthenozoospermia
|
J:314966
|
decreased sperm progressive motility
|
J:314966
|
oligozoospermia
|
J:314966
|
Ankrd31em3Flor/Ankrd31em3Flor
(C57BL/6JCrl-Ankrd31em3Flor)
|
abnormal male meiosis
|
J:314966
|
abnormal sperm head morphology
|
J:314966
|
abnormal sperm nucleus morphology
|
J:314966
|
asthenozoospermia
|
J:314966
|
decreased sperm progressive motility
|
J:314966
|
oligozoospermia
|
J:314966
|
Anks6tm1d(KOMP)Wtsi/Anks6tm1d(KOMP)Wtsi
(involves: C3H * C57BL/6 * C57BL/6N * FVB/N)
|
abnormal cholangiocyte primary cilium morphology
|
J:307271
|
Ano5em1Huyi/Ano5+
(C57BL/6N-Ano5em1Huyi)
|
abnormal osteoblast physiology
|
J:294237
|
Ano5em1Huyi/Ano5em1Huyi
(C57BL/6N-Ano5em1Huyi)
|
abnormal osteoblast physiology
|
J:294237
|
Ano5em2Huyi/Ano5em2Huyi
(C57BL/6-Ano5em2Huyi)
|
enhanced osteoblast differentiation
|
J:336715
|
Ano5tm1.2Naga/Ano5tm1.2Naga
(involves: C57BL/6)
|
decreased activated sperm motility
|
J:236134
|
decreased sperm progressive motility
|
J:236134
|
Ano5tm1Lrk/Ano5tm1Lrk
(involves: C57BL/6)
|
abnormal mitochondrial physiology
|
J:235810
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:235810
|
Ano6tm1Avor/Ano6tm1Avor
(B6.129-Ano6tm1Avor)
|
abnormal osteoblast physiology
|
J:195901
|
Anp32atm1Mak/Anp32atm1Mak
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:166683
|
Anp32btm1Mak/Anp32btm1Mak
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:172042
|
polyploidy
|
J:172042
|
Anp32etm1Mak/Anp32etm1Mak Cfdp1tm1Dkwpd/Cfdp1tm2.1Dkwpd E2f1Tg(Wnt1-cre)2Sor/E2f1+
(involves: 129 * C3H * C57BL/6)
|
abnormal intracellular organelle physiology
|
J:349245
|
Antxr1tm1.2Bstc/Antxr1tm1.2Bstc
(B6.Cg-Antxr1tm1.2Bstc)
|
abnormal extracellular matrix morphology
|
J:150947
|
Antxr1tm1.2Lepp/Antxr1tm1.2Lepp
(involves: 129 * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:150952
|
Antxr1tm1.2Lepp/Antxr1tm1.2Lepp Antxr2tm1.2Lepp/Antxr2tm1.2Lepp
(involves: 129 * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:150952
|
Antxr2tm1.1Jkit/Antxr2tm1.1Jkit
(involves: 129 * C57BL/6)
|
increased apoptosis
|
J:187210
|
Antxr2tm1.2Lepp/Antxr2tm1.2Lepp
(involves: C57BL/6)
|
decreased sensitivity to induced cell death
|
J:150952
|
Anxa1tm1Rjf/Anxa1tm1Rjf
(Not Specified)
|
impaired macrophage phagocytosis
|
J:81498
|
Anxa1tm1Rjf/Anxa1tm1Rjf
(involves: 129 * C57BL/6)
|
abnormal vascular endothelial cell migration
|
J:153690
|
decreased vascular endothelial cell proliferation
|
J:153690
|
Anxa7tm1Pll/Anxa7+
(B6.Cg-Anxa7tm1Pll)
|
chromosome breakage
|
J:93685
|
Anxa8tm1Resc/Anxa8tm1Resc Tg(Pgk1-cre)1Lni/0
(involves: 129 * C57BL/6J * BALB/c)
|
impaired leukocyte tethering or rolling
|
J:225224
|
Anxa10em1Siag/Anxa10+
(involves: C57BL/6 * DBA)
|
maternal effect
|
J:239403
|
Anxa10em1Siag/Anxa10em1Siag
(involves: C57BL/6 * DBA)
|
maternal effect
|
J:239403
|
Aoc3tm1Salm/Aoc3tm1Salm
(involves: 129S6/SvEvTac * 129S7/SvEvBrd)
|
abnormal cellular extravasation
|
J:95656
|
abnormal leukocyte adhesion
|
J:95656
|
abnormal leukocyte migration
|
J:95656
|
impaired leukocyte tethering or rolling
|
J:95656
|
Ap1b1b2b1660Clo/Ap1b1b2b1660Clo
(C57BL/6J-Ap1b1b2b1660Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
immotile respiratory cilia
|
J:175213
|
Ap1g1fgt/Ap1g1fgt
(C57BL/6-Ap1g1fgt/KjnBoc)
|
asthenozoospermia
|
J:230572
|
decreased male germ cell number
|
J:230572
|
kinked sperm flagellum
|
J:230572
|
oligozoospermia
|
J:230572
|
Ap1m2tm1.1Ohno/Ap1m2tm1.1Ohno
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
abnormal small intestinal crypt cell proliferation
|
J:226582
|
Ap1s2tm1Pschu/Y
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal fat cell differentiation
|
J:216244
|
Ap1s2tm1Pschu/Ap1s2tm1Pschu
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal fat cell differentiation
|
J:216244
|
Ap2m1tm1Ohno/Ap2m1tm1Ohno
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:102181
|
Ap3b1pe-rim2/Ap3b1pe-rim2
(involves: B10.A(R201) * C57BL/10Slc)
|
decreased platelet ATP level
|
J:42685
|
Ap3b1pe/Ap3b1pe
(B6.C3-Ap3b1pe/J)
|
abnormal lysosome morphology
|
J:152219
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:152219
|
decreased lysosomal enzyme secretion
|
J:7327
|
decreased platelet ATP level
|
J:7327
|
Ap3b1tm1Sms/Ap3b1tm1Sms
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal lysosome morphology
|
J:66256
|
Ap3d1mh/Ap3d1mh
(STOCK Mfsd12gr +/+ Ap3d1mh/J)
|
decreased lysosomal enzyme secretion
|
J:29151
|
Ap5z1tm1(KOMP)Wtsi/Ap5z1tm1(KOMP)Wtsi
(involves: 129 * C57BL/6N)
|
abnormal Golgi apparatus morphology
|
J:283611
|
abnormal Golgi stack morphology
|
J:283611
|
abnormal Golgi vesicle transport
|
J:283611
|
abnormal lysosome physiology
|
J:283611
|
impaired autophagy
|
J:283611
|
Apaf1fog/Apaf1Gt(IRESBetageo)XIX18Pgr
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C3H/HeJ * NMRI)
|
decreased neuron apoptosis
|
J:131954
|
Apaf1fog/Apaf1tm1Mak
(involves: 129S6/SvEvTac * C3H/HeJ * CD-1)
|
decreased neuron apoptosis
|
J:131954
|
Apaf1Gt(IRESBetageo)XIX18Pgr/Apaf1Gt(IRESBetageo)XIX18Pgr
(involves: 129S1/Sv * 129X1/SvJ * NMRI)
|
decreased fibroblast apoptosis
|
J:49840
|
Apaf1Gt(IRESBetageo)XIX18Pgr/Apaf1Gt(IRESBetageo)XIX18Pgr
(involves: 129/Sv * 129X1/SvJ)
|
abnormal apoptosis
|
J:103480
|
Apaf1Gt(IRESBetageo)XIX18Pgr/Apaf1Gt(IRESBetageo)XIX18Pgr
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased neuron apoptosis
|
J:112874
|
increased neuron apoptosis
|
J:112874
|
Apaf1Gt(IRESBetageo)XIX18Pgr/Apaf1Gt(IRESBetageo)XIX18Pgr Aifm1tm2Pngr/Y Foxg1tm1(cre)Skm/Foxg1+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
abnormal mitochondrial physiology
|
J:112874
|
decreased neuron apoptosis
|
J:112874
|
increased neuron apoptosis
|
J:112874
|
Apaf1tm1Her/Apaf1tm1Her
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal fibroblast apoptosis
|
J:60409
|
abnormal neuron differentiation
|
J:60409
|
abnormal spermatogonia morphology
|
J:60409
|
azoospermia
|
J:60409
|
decreased neuron apoptosis
|
J:60409
|
impaired neuronal migration
|
J:60409
|
Apaf1tm1Mak/Apaf1tm1Mak
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1))
|
abnormal respiratory electron transport chain
|
J:49841
|
decreased apoptosis
|
J:49841
|
decreased sensitivity to induced cell death
|
J:49841
|
increased cell proliferation
|
J:49841
|
Apbb1tm1Her/Apbb1tm1Her Apbb2tm1Her/Apbb2tm1Her
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal axon extension
|
J:105160
|
Apbb1tm1Trus/Apbb1tm1Trus
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:118164
|
increased cellular sensitivity to ionizing radiation
|
J:118164
|
Apc2tm1Mno/Apc2tm1Mno
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cerebellar granule cell migration
|
J:184856
|
abnormal neuronal migration
|
J:184856
|
increased neuron apoptosis
|
J:184856
|
ApcMin/Apc+
(involves: C57BL/6J)
|
abnormal enterocyte proliferation
|
J:118600
|
abnormal intestinal goblet cell morphology
|
J:118600
|
ApcMin/Apc+
((AKR/J x C57BL/6J-ApcMin)F1)
|
aneuploidy
|
J:21369
|
ApcMin/Apc+ Cd44tm1Mak/Cd44tm1Mak
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased small intestinal crypt cell apoptosis
|
J:135025
|
ApcMin/Apc+ Cd44tm1Mak/Cd44tm1Mak
(involves: C57BL/6J)
|
increased enterocyte apoptosis
|
J:204874
|
ApcMin/Apc+ Col1a1tm9(tetO-Dnmt3b_i1)Jae/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J)
|
abnormal DNA methylation
|
J:127808
|
ApcMin/Apc+ Elp3tm1.1Tac/Elp3tm1.1Tac Tg(Vil1-cre)997Gum/0
(involves: C57BL/6 * C57BL/6J * C57BL/6NTac * SJL)
|
abnormal gastrointestinal brush cell morphology
|
J:227334
|
ApcMin/Apc+ Esr1tm1.1Mma/Esr1+
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal colon goblet cell morphology
|
J:118600
|
abnormal enterocyte proliferation
|
J:118600
|
ApcMin/Apc+ Esr2tm1Mma/Esr2+
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal enterocyte proliferation
|
J:118600
|
ApcMin/Apc+ Esr2tm1Mma/Esr2tm1Mma
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal colon goblet cell morphology
|
J:118600
|
abnormal enterocyte proliferation
|
J:118600
|
ApcMin/Apc+ Foxl1tm1Khk/Foxl1tm1Khk
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:95893
|
ApcMin/Apc+ Hltftm1.1Hdin/Hltftm1.1Hdin
(involves: 129 * C57BL/6 * FVB/N)
|
chromosomal instability
|
J:252991
|
ApcMin/Apc+ Mbd4tm1Bird/Mbd4tm1Bird
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal DNA repair
|
J:77896
|
ApcMin/Apc+ Spata18tm1.2Hifa/Spata18+
(involves: C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:254117
|
ApcMin/Apc+ Spata18tm1.2Hifa/Spata18tm1.2Hifa
(involves: C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:254117
|
ApcMin/Apc+ Tgfbr1tm1Bopa/Tgfbr1+
(involves: 129S1/SvImJ * C57BL/6J)
|
increased cell proliferation
|
J:143706
|
ApcMin/ApcMin
(involves: C57BL/6J)
|
abnormal cell physiology
|
J:187862
|
ApcMin/Apctm1.1Klne
(B6.Cg-ApcMin/Apctm1.1Klne)
|
abnormal enterocyte proliferation
|
J:186132
|
Apctm1.1Alew/Apc+
(B6.129-Apctm1.1Alew)
|
increased apoptosis
|
J:180275
|
increased cell proliferation
|
J:180275
|
Apctm1.1Klne/Apctm1.1Klne
(B6.129-Apctm1.1Klne)
|
abnormal enterocyte proliferation
|
J:186132
|
Apctm1Rak/Apc+ Mbd4tm1Wed/Mbd4tm1Wed
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:80319
|
Apctm1Rfo/Apctm1Rfo
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:116121
|
Apctm1Rsmi/Apctm1Rsmi Tg(Col2a1-cre)1Rsjo/0
(involves: 129P2/OlaHsd * FVB/N)
|
enhanced osteoblast differentiation
|
J:149225
|
Apctm2.1Cip/Apc+ Atg7tm1Tchi/Atg7tm1Tchi Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2)
|
abnormal intestinal goblet cell morphology
|
J:227287
|
Apctm2.1Cip/Apc+ Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
abnormal autophagy
|
J:227287
|
Apctm2.1Cip/Apctm2.1Cip Lect2tm1Ymg/Lect2tm1Ymg Tg(Ttr-cre/Esr1*)1Vco/0
(B6.Cg-Lect2tm1Ymg Apctm2.1Cip Tg(Ttr-cre/Esr1*)1Vco)
|
increased hepatocyte apoptosis
|
J:184496
|
Apctm2.1Cip/Apctm2.1Cip Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
abnormal intestinal goblet cell morphology
|
J:98469
|
increased small intestinal crypt cell apoptosis
|
J:98469
|
Apctm2Rak/Apctm2Rak Tg(KRT14-cre)8Brn/0
(involves: 129/Sv * C57BL/6J * FVB/N * SJL)
|
abnormal cell proliferation
|
J:114152
|
abnormal keratinocyte differentiation
|
J:114152
|
Apelatm1.2Brre/Apela+
(B6(Cg)-Apelatm1.2Brre)
|
maternal effect
|
J:244834
|
Apelatm1.2Brre/Apelatm1.2Brre
(B6(Cg)-Apelatm1.2Brre)
|
increased placenta apoptosis
|
J:244834
|
maternal effect
|
J:244834
|
Apex1tm1Djc/Apex1+ Tg(TacLIZa)A1Jsh/0
(involves: 129X1/SvJ * C57BL/6 * NTac:NIHBS)
|
abnormal cell physiology
|
J:92957
|
abnormal DNA repair
|
J:92957
|
Apex1tm1Djc/Apex1tm1Djc
(involves: 129X1/SvJ * NTac:NIHS)
|
increased cellular sensitivity to gamma-irradiation
|
J:50702
|
increased embryonic epiblast cell apoptosis
|
J:50702
|
Apex1tm1Ecf/Apex1+
(either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6))
|
abnormal cell death
|
J:70397
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:70397
|
increased cellular sensitivity to oxidative stress
|
J:70397
|
Apex1tm1Ecf/Apex1+ Xpctm1Ecf/Xpctm1Ecf
(involves: 129)
|
oxidative stress
|
J:70397
|
Apex2tm1Yun/Y
(B6.129S-Apex2tm1Yun)
|
decreased splenocyte proliferation
|
J:95267
|
increased cellular sensitivity to X-ray irradiation
|
J:95267
|
Aph1atm1.1Bdes/Aph1atm1.1Bdes
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased embryonic neuroepithelium apoptosis
|
J:96106
|
AplfGt(RRF189)Byg/AplfGt(RRF189)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal DNA repair
|
J:168260
|
Apmaptm1.2Jgbs/Apmaptm1.2Jgbs
(B6.129P2-Apmaptm1.2Jgbs)
|
abnormal extracellular matrix morphology
|
J:247647
|
Apoa1tm1Bres/Apoa1+
(involves: 129S4/SvJae * C57BL/6)
|
decreased cholesterol efflux
|
J:40819
|
Apoa1tm1Bres/Apoa1tm1Bres
(involves: 129S4/SvJae * C57BL/6)
|
decreased cholesterol efflux
|
J:40819
|
Apoa1tm1Unc/Apoa1tm1Unc
(involves: 129P2/OlaHsd)
|
abnormal cellular cholesterol metabolism
|
J:120501
|
decreased cholesterol efflux
|
J:129136
|
Apoa1tm1Unc/Apoa1tm1Unc Tg(APOA1)1Rub/0
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cholesterol efflux
|
J:129136
|
Apobtm1Bres/Apob+
(involves: 129S4/SvJae * C57BL/6J)
|
asthenozoospermia
|
J:35836
|
oligozoospermia
|
J:35836
|
Apoetm1(APOE_i4)Sfu/Apoetm1(APOE_i4)Sfu
(involves: 129P2/OlaHsd)
|
abnormal plasma membrane morphology
|
J:103515
|
Apoetm1Bres/Apoetm1Bres Bcl2tm1Irt/Bcl2tm1Irt Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased macrophage apoptosis
|
J:144243
|
Apoetm1Bres/Apoetm1Bres Cx3cr1tm1Ifc/Cx3cr1tm1Ifc
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
impaired macrophage chemotaxis
|
J:81822
|
Apoetm1Bres/Apoetm1Bres Mapk9tm1Flv/Mapk9tm1Flv
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6)
|
increased macrophage derived foam cell number
|
J:94044
|
Apoetm1Unc/Apoetm1Unc
(B6.129P2-Apoetm1Unc/J)
|
abnormal osteoblast physiology
|
J:111209
|
increased cholesterol efflux
|
J:226403
|
oxidative stress
|
J:97385,
J:298071
|
Apoetm1Unc/Apoetm1Unc Ccr2tm1Ifc/Ccr2tm1Ifc
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
impaired macrophage chemotaxis
|
J:111471
|
Apoetm1Unc/Apoetm1Unc Cd36tm1Mfe/Cd36tm1Mfe
(involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6)
|
abnormal macrophage derived foam cell morphology
|
J:61672
|
Apoetm1Unc/Apoetm1Unc Cdkn1atm1Tyj/Cdkn1atm1Tyj
(B6.129-Apoetm1Unc Cdkn1atm1Tyj)
|
delayed cellular replicative senescence
|
J:125247
|
increased vascular smooth muscle cell proliferation
|
J:125247
|
Apoetm1Unc/Apoetm1Unc Cx3cl1tm1Sgs/Cx3cl1tm1Sgs
(B6.129-Apoetm1Unc Cx3cl1tm1Sgs)
|
impaired macrophage chemotaxis
|
J:95279
|
increased macrophage derived foam cell number
|
J:95279
|
Apoetm1Unc/Apoetm1Unc Cxcl10tm1Adl/Cxcl10tm1Adl
(B6.129-Cxcl10tm1Adl Apoetm1Unc)
|
impaired macrophage chemotaxis
|
J:166204
|
Apoetm1Unc/Apoetm1Unc Cyp4f13Gt(OST14770)Lex/Cyp4f13Gt(OST14770)Lex
(involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6)
|
abnormal macrophage chemotaxis
|
J:289999
|
increased cholesterol efflux
|
J:289999
|
Apoetm1Unc/Apoetm1Unc Faslpr/Faslpr
(B6.Cg-Apoetm1Unc Faslpr)
|
increased kidney apoptosis
|
J:121671
|
increased renal tubule apoptosis
|
J:121671
|
Apoetm1Unc/Apoetm1Unc Faslgld/Faslgld
(B6.Cg-Faslgld Apoetm1Unc)
|
impaired macrophage phagocytosis
|
J:91058
|
increased apoptosis
|
J:91058
|
Apoetm1Unc/Apoetm1Unc Glg1Gt(RST092)Byg/Glg1+
(B6J.129P2-Apoetm1Unc Glg1Gt(RST092)Byg)
|
impaired macrophage chemotaxis
|
J:226586
|
Apoetm1Unc/Apoetm1Unc Hptm1Alev/Hptm1Alev
(involves: 129)
|
abnormal macrophage chemotaxis
|
J:134942
|
Apoetm1Unc/Apoetm1Unc Hsd11b1tm1Lex/Hsd11b1tm1Lex
(B6.129-Hsd11b1tm1Lex Apoetm1Unc)
|
abnormal macrophage derived foam cell morphology
|
J:199430
|
Apoetm1Unc/Apoetm1Unc Il1rntm1Dih/Il1rntm1Dih
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6)
|
abnormal macrophage chemotaxis
|
J:132570
|
Apoetm1Unc/Apoetm1Unc Nfe2l2tm1Mym/Nfe2l2tm1Mym
(involves: 129P2/OlaHsd * C57BL/6J)
|
oxidative stress
|
J:143903
|
Apoetm1Unc/Apoetm1Unc Pon1tm1Lus/Pon1tm1Lus
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:82696
|
Apoetm1Unc/Apoetm1Unc Serpind1tm1Moto/Serpind1+
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
oxidative stress
|
J:122173
|
Apoetm1Unc/Apoetm1Unc Sprr3tm1.1Ppy/Sprr3tm1.1Ppy
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J * SJL)
|
increased cellular sensitivity to hydrogen peroxide
|
J:230470
|
Apoetm1Unc/Apoetm1Unc Tg(GFAP-APOE_i3)37Hol/0
(B6.Cg-Tg(GFAP-APOE_i3)37Hol Apoetm1Unc/J)
|
abnormal axon extension
|
J:93487
|
Apoetm1Unc/Apoetm1Unc Tg(GFAP-APOE_i4)22Hol/0
(B6.Cg-Apoetm1Unc Tg(GFAP-APOE_i4)22Hol)
|
abnormal axon extension
|
J:93487
|
Apoftm1(KOMP)Vlcg/Apoftm1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
decreased cholesterol efflux
|
J:185314
|
Apol6em1Hsul/Apol6em1Hsul
(Not Specified)
|
abnormal fat cell differentiation
|
J:344362
|
Apptm1.1Cep/App+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:35500
|
Apptm1.1Cep/Apptm1.1Cep
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:35500
|
Apptm1Cep/App+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:35500
|
Apptm1Cep/Apptm1Cep
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:35500
|
Apptm1Dbo/Apptm1Dbo Lrp4tm1Her/Lrp4tm1Her
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J)
|
abnormal neuron differentiation
|
J:207796
|
Apptm3.1Tcs/Apptm3.1Tcs Mapttm1.1(MAPT)Tcs/Mapttm1.1(MAPT)Tcs
(involves: 129S/SvEv * C57BL/6)
|
increased neuron apoptosis
|
J:278451
|
Appl1Gt(XM073)Byg/Appl1Gt(XM073)Byg
(B6.129P2-Appl1Gt(XM073)Byg)
|
increased T cell proliferation
|
J:164696
|
Appl1tm1.2Test/Appl1tm1.2Test
(involves: 129X1/SvJ * C57BL/6)
|
cellular phenotype
|
J:159889
|
decreased fibroblast cell migration
|
J:159889
|
increased sensitivity to induced cell death
|
J:159889
|
Appl1tm1.2Test/Appl1tm1.2Test
(involves: 129X1/SvJ)
|
abnormal cell physiology
|
J:227340
|
decreased fibroblast cell migration
|
J:227340
|
increased T cell proliferation
|
J:164696
|
Appl1tm1.2Test/Appl1tm1.2Test Appl2tm1.1Test/Appl2tm1.1Test
(involves: 129X1/SvJ)
|
abnormal cell physiology
|
J:227340
|
decreased fibroblast cell migration
|
J:227340
|
Appl2tm1.1Test/Appl2tm1.1Test
(Not Specified)
|
abnormal cell physiology
|
J:227340
|
decreased fibroblast cell migration
|
J:227340
|
Appl2tm1Smoc/Appl2tm1Smoc Tg(Ckmm-cre)5Khn/0
(involves: FVB)
|
increased skeletal muscle cell glucose uptake
|
J:230004
|
Aptxtm1Pmc/Aptxtm1Pmc
(129S4/SvJae)
|
abnormal DNA repair
|
J:170077
|
abnormal single-strand DNA break repair
|
J:145730
|
Aqp7tm1Chan/Aqp7tm1Chan
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased cellular glucose import
|
J:125011
|
Aqp8tm1Ask/Aqp8tm1Ask
(involves: C57BL/6)
|
decreased granulosa cell apoptosis
|
J:323121
|
Aqp11tm1.1Nlsn/Aqp11tm1.1Nlsn Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S1/Sv * C57BL/6 * DBA)
|
abnormal endoplasmic reticulum morphology
|
J:194939
|
ArTfm/Y
(STOCK EdaTa Atp7aMo-blo/+ +)
|
arrest of male meiosis
|
J:5173
|
ArTfm/Y
(involves: STOCK EdaTa Atp7aMo-blo)
|
arrest of male meiosis
|
J:140803
|
ArTfm/Y
(involves: NMRI * STOCK EdaTa Atp7aMo-blo)
|
arrest of male meiosis
|
J:140803
|
ArTfm/Y Tg(TSPY)9Jshm/0
(involves: NMRI * STOCK EdaTa Atp7aMo-blo)
|
arrest of male meiosis
|
J:140803
|
Artm1.1Jdz/Y
(B6.129X1-Artm1.1Jdz)
|
arrest of male meiosis
|
J:123057
|
azoospermia
|
J:123057
|
decreased male germ cell number
|
J:123057
|
Artm1.1Reb/Y
(involves: 129S4/SvJaeSor * C57BL/6 * DBA/2J)
|
arrest of male meiosis
|
J:90393
|
Artm1.1Verh/Y
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6)
|
azoospermia
|
J:88169
|
decreased male germ cell number
|
J:88169
|
increased male germ cell apoptosis
|
J:88169
|
Artm1Chc/Y Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: 129S/SvEv * C57BL/6 * SJL)
|
abnormal meiosis
|
J:118270
|
arrest of male meiosis
|
J:89886,
J:118270
|
azoospermia
|
J:89886,
J:118270
|
decreased male germ cell number
|
J:89886
|
Artm1Chc/Y Tmem163Tg(ACTB-cre)2Mrt/0
(involves: 129S/SvEv * C57BL/6J * FVB/N)
|
abnormal spermatocyte morphology
|
J:118270
|
arrest of male meiosis
|
J:118270
|
decreased spermatogonia number
|
J:81789
|
Artm1Fcl/Y
(involves: 129S2/SvPas * C57BL/6)
|
decreased germ cell number
|
J:120102
|
Artm1Jdz/Y Tg(Pbsn-cre)20Fwan/?
(involves: 129X1/SvJ * C57BL/6J * FVB/NCrl)
|
abnormal sperm flagellum morphology
|
J:137429
|
coiled sperm flagellum
|
J:137429
|
hairpin sperm flagellum
|
J:137429
|
kinked sperm flagellum
|
J:137429
|
Artm1Reb/Y
(involves: 129S4/SvJaeSor)
|
oligozoospermia
|
J:90393
|
Artm1Reb/Y Tg(Amh-cre)8815Reb/?
(involves: 129S4/SvJaeSor * FVB/N)
|
azoospermia
|
J:90393
|
Artm1Ska/Y Tg(CMV-cre)1Ipc/?
(involves: C57BL/6 * CBA)
|
cardiac interstitial fibrosis
|
J:101049
|
Artm1Verh/Y Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6)
|
abnormal spermatocyte morphology
|
J:88169
|
arrest of male meiosis
|
J:88169
|
azoospermia
|
J:88169
|
decreased elongated spermatid number
|
J:88169
|
decreased male germ cell number
|
J:88169
|
decreased round spermatid number
|
J:88169
|
increased male germ cell apoptosis
|
J:88169
|
Artm4(AR)Dmr/Y
(involves: 129S1/Sv * C57BL/6J)
|
abnormal cell cytoskeleton morphology
|
J:104360
|
oligozoospermia
|
J:104360
|
Arb2aTg(Tyr)TpNpin/Arb2aTg(Tyr)TpNpin
(involves: FVB/N)
|
abnormal neural crest cell migration
|
J:260599
|
decreased cell proliferation
|
J:260599
|
decreased neural crest cell proliferation
|
J:260599
|
increased neural crest cell apoptosis
|
J:260599
|
Arb2aTg(Tyr)TpNpin/Arb2aTg(Tyr)TpNpin Gata4tm1(cre)Svs/Gata4+
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal neural crest cell migration
|
J:260599
|
Arcn1nur17/Arcn1nur17
(involves: 129S1/SvImJ * 129S6/SvEvTac * C57BL/6J)
|
abnormal Golgi vesicle transport
|
J:160676
|
Aregtm1Dle/Aregtm1Dle Egftm1Dle/Egftm1Dle Tgfatm1Unc/Tgfatm1Unc
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:70183
|
Arfgef1Gt(CSH465)Byg/Arfgef1Gt(CSH465)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal axon extension
|
J:248338
|
abnormal axon guidance
|
J:248338
|
abnormal neuron differentiation
|
J:248338
|
delayed axon extension
|
J:248338
|
increased neuron apoptosis
|
J:248338
|
Arfgef2tm1Itl/Arfgef2tm1Itl
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac)
|
abnormal neuronal migration
|
J:187673
|
Arfgef3tm1Hong/Arfgef3tm1Hong
(129.129P2(B6)-Arfgef3tm1Hong)
|
decreased skeletal muscle cell glucose uptake
|
J:216529
|
Arfip2tm1d(EUCOMM)Wtsi/Arfip2tm1d(EUCOMM)Wtsi
(involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * CBA)
|
impaired autophagy
|
J:345639
|
Arfrp1tm1Asch/Arfrp1tm1Asch
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:142321
|
Arfrp1tm2Asch/Arfrp1tm2Asch Tg(Vil1-cre)997Gum/?
(involves: C57BL/6 * SJL)
|
abnormal cell physiology
|
J:142321
|
Arglu1tm1a(EUCOMM)Hmgu/Arglu1tm1a(EUCOMM)Hmgu
(involves: C57BL/6N)
|
increased brain apoptosis
|
J:273438
|
Arhgap1tm1Yizh/Arhgap1tm1Yizh
(involves: 129S6/SvEvTac)
|
abnormal cell morphology
|
J:101418
|
increased apoptosis
|
J:101418
|
increased fibroblast apoptosis
|
J:101418
|
increased neuron apoptosis
|
J:101418
|
Arhgap1tm1Yizh/Arhgap1tm1Yizh
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal chromosome morphology
|
J:119516
|
abnormal DNA repair
|
J:119516
|
decreased fibroblast proliferation
|
J:119516
|
Arhgap1tm1Yizh/Arhgap1tm1Yizh Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6)
|
cellular phenotype
|
J:119516
|
Arhgap17Gt(RRN062)Byg/Arhgap17Gt(RRN062)Byg
(B6.129P2-Arhgap17Gt(RRN062)Byg)
|
abnormal ileal goblet cell morphology
|
J:277297
|
Arhgap18tm1a(KOMP)Wtsi/Arhgap18tm1a(KOMP)Wtsi
(C57BL/6-Arhgap18tm1a(KOMP)Wtsi)
|
abnormal actin cytoskeleton morphology
|
J:267328
|
Arhgap25tm1a(KOMP)Wtsi/Arhgap25tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal cellular extravasation
|
J:240521
|
enhanced leukocyte migration
|
J:240521
|
enhanced leukocyte tethering or rolling
|
J:240521
|
Arhgap26Gt(OST135790)Lex/Arhgap26Gt(OST135790)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal myoblast fusion
|
J:215392
|
Arhgap32tm1Taki/Arhgap32tm1Taki
(involves: C57BL/6 * C57BL/6N * CBA)
|
abnormal neuron differentiation
|
J:116446
|
Arhgap35m1Bchd/Arhgap35m1Bchd
(involves: C3H/HeNCrl * C57BL/6J)
|
abnormal cilium morphology
|
J:232342
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:232342
|
Arhgap45em1Ciphe/Arhgap45em1Ciphe
(C57BL/6-Arhgap45em1Ciphe)
|
decreased lymphocyte chemotaxis
|
J:309971
|
Arhgdiatm1Ytk/Arhgdiatm1Ytk
(involves: 129S/SvEv * C57BL/6 * DBA)
|
decreased mesangial cell number
|
J:57995
|
oligozoospermia
|
J:57995
|
Arhgdiatm1Ytk/Arhgdiatm1Ytk Arhgdibtm1Miyo/Arhgdibtm1Miyo
(involves: 129S/SvEv)
|
decreased T cell proliferation
|
J:140671
|
enhanced B cell migration
|
J:140671
|
increased B cell proliferation
|
J:140671
|
Arhgdibtm1Len/Arhgdibtm1Len
(involves: 129S4/SvJae * C57BL/6)
|
increased B cell proliferation
|
J:42604
|
Arhgef1tm1Kdf/Arhgef1tm1Kdf
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased B cell proliferation
|
J:99463
|
increased T cell proliferation
|
J:99463
|
Arhgef2Gt(IST13976A8)Tigm/Arhgef2Gt(IST13976A8)Tigm
(involves: C57BL/6N)
|
abnormal neuronal migration
|
J:242973
|
Arhgef4tm1Taki/Arhgef4tm1Taki
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal vascular endothelial cell migration
|
J:159959
|
Arhgef6tm1Kdf/Arhgef6tm1Kdf
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:137269
|
decreased T cell proliferation
|
J:137269
|
enhanced B cell migration
|
J:137269
|
Arhgef7tm1c(EUCOMM)Wtsi/Arhgef7tm1c(EUCOMM)Wtsi Tg(Ttr-cre)1Hadj/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
abnormal anterior visceral endoderm cell migration
|
J:217373
|
Arhgef7tm1d(EUCOMM)Wtsi/Arhgef7tm1d(EUCOMM)Wtsi
(involves: C57BL/6N * CBA)
|
abnormal anterior visceral endoderm cell migration
|
J:217373
|
Arhgef7tm1Dprk/Arhgef7tm1Dprk
(involves: 129S4/SvJae * C57BL/6J)
|
decreased fibroblast chemotaxis
|
J:284300
|
increased fibroblast cell migration
|
J:284300
|
Arhgef11tm1.1Mak/Arhgef11tm1.1Mak
(B6.129P2(C)-Arhgef11tm1.1Mak)
|
abnormal white fat cell differentation
|
J:233950
|
Arhgef11tm1Sgkd/Arhgef11tm1Sgkd Arhgef12tm1Sgkd/Arhgef12tm1Sgkd
(involves: 129 * C57BL/6J)
|
abnormal fibroblast proliferation
|
J:198274
|
decreased fibroblast proliferation
|
J:198274
|
Arhgef12tm1.1Wet/Arhgef12tm1.1Wet Tg(Lck-cre)548Jxm/0
(involves: 129 * C57BL/6 * CBA)
|
abnormal T cell proliferation
|
J:149560
|
Arhgef15tm1(KOMP)Vlcg/Arhgef15tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal vascular regression
|
J:188649
|
Arhgef28tm1.1Ddsr/Arhgef28tm1.1Ddsr
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac * BALB/cJ)
|
decreased fibroblast cell migration
|
J:221026
|
Arid1atm1.1Mag/Arid1atm1.1Mag Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S4/SvJaeSor * C57BL/6J * CBA/J)
|
abnormal cardiac neural crest cell migration
|
J:231470
|
abnormal neural crest cell migration
|
J:231470
|
Arid1atm1.1Mag/Arid1atm1.1Mag H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: C57BL/6J * CBA/J)
|
abnormal cardiac neural crest cell migration
|
J:231470
|
Arid2tm1a(EUCOMM)Wtsi/Arid2tm1a(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
decreased fetal cardiomyocyte proliferation
|
J:223458
|
Arid3atm1Pwt/Arid3atm1Pwt
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell physiology
|
J:197237
|
Arid3btm1Take/Arid3btm1Take
(B6.Cg-Arid3btm1Take)
|
abnormal vascular regression
|
J:108390
|
increased apoptosis
|
J:108390
|
Arid4atm1Alb/Arid4atm1Alb
(involves: 129S7/SvEvBrd * C57BL/6)
|
genetic imprinting
|
J:113402
|
Arid4atm1Alb/Arid4atm1Alb
(involves: 129S7/SvEvBrd)
|
abnormal mononuclear cell differentiation
|
J:141004
|
Arid4atm1Alb/Arid4atm1Alb Arid4btm1Alb/Arid4b+
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal DNA methylation during gametogenesis
|
J:113402
|
abnormal imprinting
|
J:113402
|
maternal imprinting
|
J:113402
|
Arid4atm1Alb/Arid4atm1Alb Rr70tm1Alb/Rr70+
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal DNA methylation
|
J:113402
|
abnormal imprinting
|
J:113402
|
Arid4btm1Alb/Arid4b+
(involves: 129S7/SvEvBrd * C57BL/6)
|
genetic imprinting
|
J:113402
|
Arid4btm1Alb/Arid4b+ Rr70tm1Alb/Rr70+
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal DNA methylation
|
J:113402
|
abnormal imprinting
|
J:113402
|
Arid4btm1Alb/Arid4btm1.1Mywu Tg(Amh-cre)8815Reb/0
(involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)
|
azoospermia
|
J:233398
|
decreased elongated spermatid number
|
J:233398
|
decreased male germ cell number
|
J:233398
|
decreased round spermatid number
|
J:233398
|
decreased spermatid number
|
J:233398
|
decreased spermatogonia number
|
J:233398
|
increased testis apoptosis
|
J:233398
|
Arid5bGt(ROSA)75Sor/Arid5bGt(ROSA)75Sor
(involves: 129S4/SvJaeSor)
|
abnormal cell migration
|
J:117491
|
decreased fibroblast cell migration
|
J:117491
|
Arih2tm1Mak/Arih2tm1Mak
(B6.129P2-Arih2tm1Mak)
|
increased apoptosis
|
J:191066
|
Ark2cGt(P9-3F)Sor/Ark2cGt(P9-3F)Sor Tg(Hlxb9-GFP)1Tmj/0
(involves: 129S4/SvJaeSor * C57BL/6 * CBA)
|
abnormal axon extension
|
J:198828
|
Arl2bpem1Visu/Arl2bpem1Visu
(involves: 129S2/SvPasCrl * C57BL/6J * FVB/N)
|
abnormal photoreceptor connecting cilium morphology
|
J:280811
|
Arl2bpem1Visu/Arl2bpem1Visu
(involves: FVB/N)
|
abnormal acrosome morphology
|
J:279003
|
abnormal primary cilium morphology
|
J:279003
|
abnormal sperm axoneme morphology
|
J:279003
|
abnormal sperm fibrous sheath morphology
|
J:279003
|
abnormal sperm flagellum morphology
|
J:279003
|
abnormal sperm head morphology
|
J:279003
|
abnormal sperm midpiece morphology
|
J:279003
|
abnormal sperm mitochondrial sheath morphology
|
J:279003
|
abnormal spermatid morphology
|
J:279003
|
coiled sperm flagellum
|
J:279003
|
detached sperm flagellum
|
J:279003
|
immotile sperm
|
J:279003
|
oligozoospermia
|
J:279003
|
short sperm flagellum
|
J:279003
|
teratozoospermia
|
J:279003
|
Arl3Gt(EUCJ0159b07)1.1Hmgu/Arl3Gt(EUCJ0159b07)1.1Hmgu Tg(Six3-cre)69Frty/0
(involves: C57BL/6N * DBA/2)
|
abnormal photoreceptor connecting cilium morphology
|
J:232436
|
Arl4atm1Asch/Arl4atm1Asch
(involves: C57BL/6J)
|
decreased male germ cell number
|
J:75778
|
oligozoospermia
|
J:75778
|
Arl6tm2Vcs/Arl6tm2Vcs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal brain ependyma motile cilium morphology
|
J:180524
|
abnormal brain ependyma motile cilium physiology
|
J:180524
|
absent sperm flagellum
|
J:180524
|
cellular phenotype
|
J:180524
|
decreased brain ependyma motile cilium number
|
J:180524
|
Arl6ip5tm1Tnkk/Arl6ip5tm1Tnkk
(either: B6.Cg-Arl6ip5tm1Tnkk or (involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj))
|
abnormal redox activity
|
J:182338
|
Arl13btm1.1Tc/Arl13btm1.1Tc Pde6gtm1(cre/ERT2)Eye/Pde6g+
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal photoreceptor connecting cilium morphology
|
J:272501
|
Arl13btm1.1Tc/Arl13btm1.1Tc Tg(Six3-cre)69Frty/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA/2)
|
abnormal photoreceptor connecting cilium morphology
|
J:272501
|
Arl13btm1c(EUCOMM)Wtsi/Arl13btm1c(EUCOMM)Wtsi Tg(Cdh16-cre)91Igr/0
(involves: C57BL/6J * C57BL/6N * ICR)
|
absent kidney epithelial cell primary cilium
|
J:240795
|
increased kidney cell proliferation
|
J:240795
|
Armc2em1Pfr/Armc2em1Pfr
(Not Specified)
|
abnormal sperm flagellum morphology
|
J:279937
|
absent sperm axonemal central pair
|
J:279937
|
absent sperm flagellum
|
J:279937
|
coiled sperm flagellum
|
J:279937
|
immotile sperm
|
J:279937
|
oligozoospermia
|
J:279937
|
short sperm flagellum
|
J:279937
|
teratozoospermia
|
J:279937
|
thick sperm flagellum
|
J:279937
|
Armc3em1Lukf/Armc3em1Lukf
(C57BL/6J-Armc3em1Lukf)
|
abnormal spermatid morphology
|
J:308934
|
immotile sperm
|
J:308934
|
impaired autophagy
|
J:308934
|
oligozoospermia
|
J:308934
|
Armc12em1Osb/Armc12em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
decreased sperm progressive motility
|
J:302631
|
disorganized sperm mitochondrial sheath
|
J:302631
|
kinked sperm flagellum
|
J:302631
|
Armc12em1Osb/Armc12em1Osb Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
(involves: C57BL/6NJcl * DBA/2NJcl)
|
impaired sperm migration in female genital tract
|
J:302631
|
Armc12em3Osb/Armc12em3Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm mitochondrial sheath morphology
|
J:302631
|
kinked sperm flagellum
|
J:302631
|
Arnt2tm1Mcs/Arnt2tm1Mcs
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:69874
|
Arnttm1.1Gonz/Arnttm1.2Gonz Tg(KRT5-cre)1Tak/0
(involves: 129X1/SvJ * C3H * C57BL/6)
|
increased keratinocyte apoptosis
|
J:86533
|
Arnttm1Bra/Arnttm1Bra
(involves: 129)
|
patent ductus venosus
|
J:94465
|
Arnttm1Mcs/Arnttm1Mcs
(involves: 129S1/Sv * 129X1/SvJ)
|
cellular phenotype
|
J:39730,
J:66515
|
Arpc3Gt(XG476)Byg/Arpc3Gt(XG476)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal fibroblast chemotaxis
|
J:185040
|
abnormal fibroblast physiology
|
J:185040
|
impaired fibroblast cell migration
|
J:185040
|
Arpc3Tn(sb-lacZ,GFP)T5.117Jtak/Arpc3Tn(sb-lacZ,GFP)T5.117Jtak
(Not Specified)
|
abnormal cell morphology
|
J:111402
|
Arpc4tm1c(EUCOMM)Wtsi/Arpc4tm1c(EUCOMM)Wtsi Krt14tm1(cre)Wbm/Krt14+
(B6.Cg-Arpc4tm1c(EUCOMM)Wtsi Krt14tm1(cre)Wbm)
|
abnormal keratinocyte differentiation
|
J:253986
|
Arrb1tm1Jse/Arrb1tm1Jse Arrb2tm1Rjl/Arrb2tm1Rjl
(involves: 129X1/SvJ * C57BL/6)
|
decreased mesenchymal cell proliferation involved in lung development
|
J:159121
|
Arrdc1tm1(KOMP)Vlcg/Arrdc1tm1(KOMP)Vlcg
(involves: C57BL/6N * C57BL/6NTac)
|
abnormal cell physiology
|
J:236091
|
Arrdc4tm1(KOMP)Vlcg/Arrdc4tm1(KOMP)Vlcg
(involves: C57BL/6N * C57BL/6NTac)
|
abnormal cell physiology
|
J:236091
|
Arrdc5em1Oat/Arrdc5em1Oat
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal acrosome morphology
|
J:336766
|
asthenozoospermia
|
J:336766
|
enlarged sperm head
|
J:336766
|
oligozoospermia
|
J:336766
|
teratozoospermia
|
J:336766
|
Arsatm1Gie/Arsatm1Gie
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal lysosome morphology
|
J:178538
|
abnormal male germ cell morphology
|
J:178538
|
abnormal sperm head morphology
|
J:178538
|
abnormal spermatid morphology
|
J:178538
|
coiled sperm flagellum
|
J:178538
|
increased male germ cell apoptosis
|
J:178538
|
oligozoospermia
|
J:178538
|
teratozoospermia
|
J:178538
|
Arsbm1J/Arsbm1J
(C57BL/6J-Arsbm1J/GrsrJ)
|
abnormal lysosome physiology
|
J:149960
|
Arsbtm1Cptr/Arsbtm1Cptr
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell morphology
|
J:34831
|
Arsbtm1Cptr/Arsbtm1Cptr
(involves: 129P2/OlaHsd * 129S2/SvPas)
|
abnormal cell morphology
|
J:102290
|
Arsgtm1Tdi/Arsgtm1Tdi
(involves: 129S2/SvPas * C57BL/6)
|
lysosomal protein accumulation
|
J:185592
|
Arsktm1b(KOMP)Wtsi/Arsktm1b(KOMP)Wtsi
(B6N(Cg)-Arsktm1b(KOMP)Wtsi/J)
|
abnormal lysosome physiology
|
J:302659
|
Art2atm1Fkn/Art2atm1Fkn Art2btm1Fkn/Art2btm1Fkn
(NOD.129S4(B6)-Art2atm1Fkn Art2btm1Fkn/Lt)
|
decreased T cell apoptosis
|
J:108097
|
Arv1tm1.2Radr/Arv1tm1.2Radr
(involves: 129S1/Sv * 129X1/SvJ * BALB/cJ)
|
increased fatty acid oxidation
|
J:241193
|
Arxtm1.1Ics/Y
(involves: 129S2/SvPas * C57BL/6J * C57BL/6N)
|
abnormal neuronal migration
|
J:262482
|
Arxtm1Kki/Y
(involves: 129P2/OlaHsd * C57BL)
|
impaired neuronal migration
|
J:79871
|
Arxtm2Kki/Y
(involves: 129S/SvEv * C57BL/6J)
|
abnormal neuronal migration
|
J:152416
|
Arxtm3Kki/Y
(involves: 129S/SvEv * C57BL/6J)
|
abnormal neuronal migration
|
J:152416
|
Arxtm4Kki/Y
(involves: 129S/SvEv * C57BL/6J)
|
abnormal neuronal migration
|
J:152416
|
Asah1tm1.1Jhkh/Asah1+ Smpd1tm1Esc/Smpd1+
(involves: 129S1/Sv)
|
abnormal neuron differentiation
|
J:199833
|
Asah1tm1.1Jhkh/Asah1tm1.1Jhkh
(Not Specified)
|
abnormal neuron differentiation
|
J:199833
|
Asah1tm1.2Geno/Asah1tm1.2Geno
(involves: C57BL/6)
|
increased macrophage derived foam cell number
|
J:285931
|
Asah1tm1Medin/Asah1tm1Medin
(involves: 129S6/SvEvTac * CD-1)
|
abnormal lysosome morphology
|
J:232306
|
increased macrophage derived foam cell number
|
J:232306
|
Asap1Gt(RRS873)Byg/Asap1Gt(RRS873)Byg
(FVB.129P2(B6)-Asap1Gt(RRS873)Byg)
|
abnormal cell differentiation
|
J:277387
|
abnormal fat cell differentiation
|
J:277387
|
Asb17em1Bzhg/Asb17em1Bzhg
(involves: CD-1)
|
oligozoospermia
|
J:324157
|
Ascl1tm1(Neurog2)Fgu/Ascl1tm1(Neurog2)Fgu
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron apoptosis
|
J:109482
|
Ascl1tm1And/Ascl1tm1And
(involves: 129)
|
abnormal neuron apoptosis
|
J:109482
|
decreased neuronal precursor proliferation
|
J:203419
|
impaired neuron differentiation
|
J:203419
|
Ascl1tm1And/Ascl1tm1And Neurod1tm1Jle/Neurod1tm1Jle Neurod4tm1Kag/Neurod4tm1Kag
(involves: 129/Sv * C57BL/6 * CBA * ICR)
|
increased retina apoptosis
|
J:121047
|
Ascl1tm1And/Ascl1tm1And Neurod4tm1Kag/Neurod4tm1Kag
(either: (involves: 129S2/SvPas * C57BL/6 * CBA) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA))
|
abnormal neuron differentiation
|
J:65410
|
Ascl1tm2Fgu/Ascl1tm2Fgu
(Not Specified)
|
abnormal neuronal migration
|
J:174732
|
Ascl2tm1.1Cle/Ascl2tm1.1Cle Tg(Cyp1a1-cre)1Dwi/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
increased small intestinal crypt cell apoptosis
|
J:148715
|
Ascl2tm1Alj/Ascl2+
(involves: 129 * CD-1)
|
paternal imprinting
|
J:23260
|
Ascl2tm1Alj/Ascl2+ Kcnq1ot1tm1.1Mjh/Kcnq1ot1+
(involves: 129 * C57BL/6 * ICR)
|
abnormal imprinting
|
J:130399
|
Ash2lGt(S3-11A1)Sor/Ash2lGt(S3-11A1)Sor
(involves: 129S4/SvJaeSor * C57BL/6J)
|
abnormal cell physiology
|
J:162660
|
Asic3tm1Pho/Asic3tm1Pho
(involves: C57BL/6)
|
abnormal retina apoptosis
|
J:151049
|
Asnsd1Gt(OST460318)Lex/Asnsd1Gt(OST460318)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal cell differentiation
|
J:320329
|
Aspmem1Mama/Aspmem1Mama
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal male germ cell physiology
|
J:310617
|
cellular phenotype
|
J:310617
|
AspmGt(AA0137)Wtsi/AspmGt(AA0137)Wtsi
(involves: 129P2/OlaHsd * C57BL/6JOlaHsd)
|
asthenozoospermia
|
J:164424
|
oligozoospermia
|
J:164424
|
small sperm head
|
J:164424
|
AspmGt(AJ0069)Wtsi/AspmGt(AJ0069)Wtsi
(involves: 129P2/OlaHsd * C57BL/6JOlaHsd)
|
asthenozoospermia
|
J:164424
|
oligozoospermia
|
J:164424
|
small sperm head
|
J:164424
|
Aspmtm1(cre)Mrc/Aspmtm1(cre)Mrc
(Not Specified)
|
abnormal cell cycle
|
J:228026
|
Aspmtm1.2Kxi/Aspmtm1.2Kxi
(involves: C57BL * C57BL/6J * DBA)
|
oligozoospermia
|
J:205524
|
Aspscr1tm1.1Jsbo/Aspscr1tm1.1Jsbo Tg(Ckmm-cre)5Khn/0
(B6.Cg-Aspscr1tm1.1Jsbo Tg(Ckmm-cre)5Khn)
|
decreased fatty acid oxidation
|
J:308358
|
disorganized mitochondrial cristae
|
J:308358
|
increased skeletal muscle cell glucose uptake
|
J:308358
|
increased skeletal muscle fiber mitochondrial size
|
J:308358
|
Asrgl1em1Xjz/Asrgl1em1Xjz
(C57BL/6J-Asrgl1em1Xjz)
|
increased retina apoptosis
|
J:320011
|
Ass1bar/Ass1bar
(FVB.BAR-Ass1bar)
|
abnormal cerebellar granule cell migration
|
J:165341
|
Ass1bar/Ass1bar
(B6.BAR-Ass1bar)
|
abnormal cerebellar granule cell migration
|
J:165341
|
Ass1bar/Ass1fold
(involves: C57BL/6Ei * C57BL/6J * OF1 * P/J)
|
abnormal cerebellar granule cell migration
|
J:165341
|
Ass1fold/Ass1fold
(B6Ei.P-Ass1fold/GrsrJ)
|
abnormal cerebellar granule cell migration
|
J:165341
|
oxidative stress
|
J:165341
|
Astn1tm1Hatn/Astn1tm1Hatn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cerebellar granule cell migration
|
J:74969
|
increased neuron apoptosis
|
J:74969
|
Asxl1tm1.1Mjxu/Asxl1+
(involves: 129 * C57BL/6)
|
increased apoptosis
|
J:208085
|
increased cell proliferation
|
J:208085
|
Asxl1tm1.1Mjxu/Asxl1tm1.1Mjxu
(involves: 129 * C57BL/6)
|
increased apoptosis
|
J:208085
|
increased cell proliferation
|
J:208085
|
Asxl2Gt(AQ0356)Wtsi/Asxl2Gt(AQ0356)Wtsi
(involves: 129P2/OlaHsd * C57BL/6J)
|
cardiac interstitial fibrosis
|
J:147372
|
Asz1tm1Zuk/Asz1tm1Zuk
(involves: 129 * C57BL/6)
|
abnormal DNA methylation during gametogenesis
|
J:152071
|
abnormal male meiosis
|
J:152071
|
abnormal spermatocyte morphology
|
J:152071
|
chromosomal instability
|
J:152071
|
at/at
(involves: DBA/1oHu)
|
abnormal oocyte number
|
J:125484
|
decreased male germ cell number
|
J:6193,
J:13446
|
decreased oocyte number
|
J:13446
|
Atad3atm1c(KOMP)Wtsi/Atad3atm1c(KOMP)Wtsi Myl1tm1(cre)Sjb/Myl1+
(B6J.Cg-Myl1tm1(cre)Sjb Atad3atm1c(KOMP)Wtsi)
|
abnormal mitochondrial crista morphology
|
J:263681
|
abnormal muscle fiber mitochondrial morphology
|
J:263681
|
abnormal oxidative phosphorylation
|
J:263681
|
decreased mitochondrial size
|
J:263681
|
decreased skeletal muscle fiber mitochondrial DNA content
|
J:263681
|
disorganized mitochondrial cristae
|
J:263681
|
Atad5Gt(RRF055)Byg/Atad5+
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:176672
|
abnormal DNA repair
|
J:176672
|
aneuploidy
|
J:176672
|
chromosomal instability
|
J:176672
|
Atat1tm1(KOMP)Vlcg/Atat1tm1(KOMP)Vlcg
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal cell physiology
|
J:201922
|
Atat1tm1.2Phep/Atat1tm1.2Phep
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6J)
|
abnormal cell morphology
|
J:205737
|
abnormal sperm annulus morphology
|
J:205737
|
asthenozoospermia
|
J:205737
|
increased male germ cell apoptosis
|
J:205737
|
oligozoospermia
|
J:205737
|
short sperm flagellum
|
J:205737
|
teratozoospermia
|
J:205737
|
Ate1tm1Avar/Ate1tm1Avar
(either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J))
|
abnormal vascular regression
|
J:77750
|
Ate1tm1Avar/Ate1tm2.1Avar Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S1/Sv * C57BL/6 * CBA)
|
abnormal cell physiology
|
J:155421
|
abnormal spermatid morphology
|
J:155421
|
decreased male germ cell number
|
J:155421
|
Atf1tm1Gsc/Atf1+ Creb1tm2Gsc/Creb1tm2Gsc
(involves: 129/Sv * 129P2/SvPas * C57BL/6)
|
abnormal apoptosis
|
J:74982
|
Atf1tm1Gsc/Atf1tm1Gsc Creb1tm2Gsc/Creb1tm2Gsc
(involves: 129/Sv * 129P2/SvPas * C57BL/6)
|
abnormal apoptosis
|
J:74982
|
Atf1tm1Gsc/Atf1tm1Gsc Creb1tm3Gsc/Creb1tm3Gsc Tg(Dbh-icre)1Gsc/0
(involves: 129 * 129P2/OlaHsd * C57BL/6)
|
decreased neuron apoptosis
|
J:121244
|
Atf2tm1Sis/Atf2+ Creb5tm1Sis/Creb5+
(involves: C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:156376
|
Atf2tm1Sis/Atf2tm1Sis Creb5tm1Sis/Creb5tm1Sis
(involves: C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:156376
|
Atf2tm2Nicj/Atf2tm2Nicj Atf7tm1Nicj/Atf7tm1Nicj
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cell proliferation
|
J:123909
|
increased apoptosis
|
J:123909
|
increased hepatocyte apoptosis
|
J:123909
|
Atf4tm1Aki/Atf4tm1Aki
(involves: 129P2/OlaHsd)
|
increased lens epithelium apoptosis
|
J:56007
|
Atf4tm1Tow/Atf4+ Ptprvtm1Asmi/Ptprv+
(either: (involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J * NIH Black Swiss) or (involves: 129P2/OlaHsd * C57BL/6J * NIH Black Swiss))
|
increased pancreatic beta cell proliferation
|
J:152695
|
Atf4tm1Tow/Atf4tm1Tow
(involves: 129S1/Sv * 129X1/SvJ * NIH Black Swiss)
|
decreased cell proliferation
|
J:74479
|
Atf4tm1Tow/Atf4tm1Tow
(either: (involves: 129P2/OlaHsd * NIH Black Swiss) or (involves: 129S1/Sv * 129X1/SvJ * NIH Black Swiss))
|
abnormal osteoblast differentiation
|
J:129974
|
Atf4tm1Tow/Atf4tm1Tow
(either: (involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J * NIH Black Swiss) or (involves: 129P2/OlaHsd * C57BL/6J * NIH Black Swiss))
|
increased pancreatic beta cell proliferation
|
J:152695
|
Atf6tm1.1Rjk/Atf6tm1.1Rjk
(involves: C57BL/6 * FVB/N)
|
abnormal cell physiology
|
J:124971
|
abnormal endoplasmic reticulum physiology
|
J:124971
|
decreased cell proliferation
|
J:124971
|
Atf6tm1Hota/Atf6tm1Hota Tg(Ins2-cre)25Mgn/0
(B6.Cg-Atf6tm1Hota Tg(Ins2-cre)25Mgn)
|
increased pancreatic islet cell apoptosis
|
J:213542
|
Atf6tm1Kamo/Atf6tm1Kamo
(involves: 129S4/SvJae * C57BL/6J)
|
increased sensitivity to induced cell death
|
J:145116
|
Atf6btm1Kamo/Atf6btm1Kamo
(involves: 129S4/SvJae * C57BL/6J)
|
increased sensitivity to induced cell death
|
J:145116
|
Atg3tm1.1Ywh/Atg3tm1.1Ywh Fnip1m1Btlr/Fnip1m1Btlr Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal autophagy
|
J:234285
|
Atg3tm1.1Ywh/Atg3tm1.1Ywh Gt(ROSA)26Sortm1(cre/ERT)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJaeSor * C57BL/6)
|
increased T cell apoptosis
|
J:172749
|
Atg3tm1.1Ywh/Atg3tm1.1Ywh Tg(Lck-cre)548Jxm/0
(involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA)
|
decreased T cell proliferation
|
J:172749
|
impaired autophagy
|
J:172749
|
increased T cell apoptosis
|
J:172749
|
oxidative stress
|
J:172749
|
Atg3tm1Kmts/Atg3+
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal autophagosome formation
|
J:215884
|
Atg3tm1Kmts/Atg3tm1Kmts
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal autophagy
|
J:215884
|
Atg4bGt(A029E06)Wrst/Atg4bGt(A029E06)Wrst
(involves: 129S2/SvPas * C57BL/6)
|
impaired autophagy
|
J:163712
|
Atg4ctm1Otin/Atg4ctm1Otin
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired autophagy
|
J:123386
|
Atg4dGt(OST254045)Lex/Atg4dGt(OST254045)Lex Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129S5/SvEvBrd * C57BL/6J * C57BL/6NCrlj * DBA/2J)
|
abnormal autophagosome formation
|
J:313858
|
Atg5tm1.1Myok/Atg5tm1.1Myok Col1a1tm3(tetO-Pou5f1,-Sox2,-Klf4,-Myc)Jae/Col1a1+
(involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal cell physiology
|
J:205532
|
Atg5tm1Myok/Atg5tm1Myok
(involves: 129S/SvEv)
|
cellular phenotype
|
J:232686
|
Atg5tm1Myok/Atg5tm1Myok Cnot3tm1.1Kjkb/Cnot3tm1.1Kjkb Tg(Ckmm-cre)5Khn/0
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6 * FVB)
|
abnormal autophagosome formation
|
J:260012
|
Atg5tm1Myok/Atg5tm1Myok Tg(BEST1-cre)1Taf/0
(involves: 129S/SvEv * C57BL/6J)
|
abnormal autophagy
|
J:200084
|
Atg5tm1Myok/Atg5tm1Myok Tg(CAG-EGFP/Map1lc3b)53Nmz/0 Tg(Cryaa-cre)10Mlr/0
(involves: 129S/SvEv * C57BL/6 * DBA/2 * FVB/N)
|
impaired autophagy
|
J:198392
|
Atg5tm1Myok/Atg5tm1Myok Tg(Kap-cre)1Isa/0
(involves: 129S/SvEv * C57BL/6 * DBA)
|
impaired autophagy
|
J:179961
|
Atg5tm1Myok/Atg5tm1Myok Tg(Nes-cre)1Kln/?
(involves: 129S/SvEv * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:110050
|
Atg5tm1Myok/Atg5tm1Myok Tg(Pomc1-cre)1Gsb/0
(involves: 129S/SvEv * C57BL/6 * FVB/N)
|
abnormal autophagy
|
J:232686
|
Atg5tm1Myok/Atg5tm1Myok Tg(Stra8-icre)1Reb/0
(involves: 129S/SvEv * FVB/NJ)
|
abnormal acrosome assembly
|
J:307712
|
abnormal sperm end piece morphology
|
J:307712
|
abnormal sperm flagellum morphology
|
J:307712
|
abnormal sperm head morphology
|
J:307712
|
abnormal sperm midpiece morphology
|
J:307712
|
abnormal sperm mitochondrial sheath morphology
|
J:307712
|
abnormal sperm nucleus morphology
|
J:307712
|
absent sperm fibrous sheath
|
J:307712
|
asthenozoospermia
|
J:307712
|
double-headed sperm
|
J:307712
|
globozoospermia
|
J:307712
|
immotile sperm
|
J:307712
|
impaired autophagy
|
J:307712
|
multinucleated giant male germ cells
|
J:307712
|
oligozoospermia
|
J:307712
|
short sperm flagellum
|
J:307712
|
teratozoospermia
|
J:307712
|
Atg5tm1Myok/Atg5tm1Myok Tg(Vil1-cre)997Gum/0
(involves: 129S/SvEv * C57BL/6 * SJL)
|
impaired autophagy
|
J:141419
|
Atg5tm1Myok/Atg5tm1Myok Tg(Vil1-cre)1000Gum/0
(involves: 129S/SvEv * C57BL/6J * SJL/J)
|
abnormal intestinal goblet cell morphology
|
J:206181
|
Atg5tm1Nmz/Atg5tm1Nmz
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal lysosome morphology
|
J:104491
|
Atg5tm1Nmz/Atg5tm1Nmz Tg(CAG-EGFP/Map1lc3b)53Nmz/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal autophagosome formation
|
J:140583
|
Atg5tm1Nmz/Atg5tm1Nmz Tg(Cd4-cre)1Cwi/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:211733
|
impaired autophagy
|
J:211733
|
increased mitochondrial size
|
J:211733
|
oxidative stress
|
J:211733
|
Atg7tm1.1Tchi/Atg7tm1.1Tchi
(involves: C57BL/6 * CBA * FVB/N)
|
abnormal intracellular organelle morphology
|
J:100199
|
Atg7tm1Tchi/Atg7tm1Tchi Aviltm2(cre)Fawa/Avil+
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
increased neuron apoptosis
|
J:160568
|
Atg7tm1Tchi/Atg7tm1Tchi Cnot3tm1.1Kjkb/Cnot3tm1.1Kjkb Tg(Ckmm-cre)5Khn/0
(involves: 129P2/OlaHsd * C57BL/6NCrlj * CBA/JNCrlj * FVB)
|
abnormal autophagosome formation
|
J:260012
|
Atg7tm1Tchi/Atg7tm1Tchi Sqstm1tm1Keta/Sqstm1tm1Keta Tg(Nes-cre)1Wme/0
(involves: 129 * C57BL/6 * C57BL/6NCrlj * CBA * CBA/JNCrlj)
|
increased neuron apoptosis
|
J:130839
|
Atg7tm1Tchi/Atg7tm1Tchi Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal autophagosome formation
|
J:258511
|
Atg7tm1Tchi/Atg7tm1Tchi Tg(Camk2a-cre)T29-1Stl/0
(involves: BALB/c * C57BL * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
impaired autophagy
|
J:217829
|
Atg7tm1Tchi/Atg7tm1Tchi Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal hepatocyte mitochondrial morphology
|
J:100199
|
impaired autophagy
|
J:130839
|
increased hepatocyte proliferation
|
J:130839
|
Atg7tm1Tchi/Atg7tm1Tchi Tg(Nes-cre)1Kln/0
(involves: C57BL/6NCrlj * CBA/JNCrlj * SJL)
|
abnormal endoplasmic reticulum morphology
|
J:298097
|
cellular phenotype
|
J:298097
|
Atg7tm1Tchi/Atg7tm1Tchi Tg(Nes-cre)1Kln/0 Wdr45btm1c(EUCOMM)Hmgu/Wdr45btm1c(EUCOMM)Hmgu
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * SJL)
|
abnormal endoplasmic reticulum morphology
|
J:298097
|
abnormal Golgi apparatus morphology
|
J:298097
|
Atg7tm1Tchi/Atg7tm1Tchi Tg(Nes-cre)1Wme/0
(involves: C57BL/6 * CBA)
|
impaired autophagy
|
J:130839
|
increased neuron apoptosis
|
J:130839
|
Atg7tm1Tchi/Atg7tm1Tchi Tg(Tyr-cre)1Lru/Y
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2)
|
abnormal autophagy
|
J:220623
|
abnormal melanocyte proliferation
|
J:220623
|
dilated mitochondrion
|
J:220623
|
early cellular replicative senescence
|
J:220623
|
oxidative stress
|
J:220623
|
Atg7tm1Tchi/Atg7tm1Tchi Tg(Vil1-cre)1000Gum/0
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj * SJL/J)
|
abnormal intestinal goblet cell morphology
|
J:206181
|
Atg7tm1Tchi/Atg7tm1Tchi Xbp1tm2Glm/Xbp1tm2Glm Tg(Vil1-cre)997Gum/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL)
|
abnormal autophagy
|
J:206084
|
Atg9atm1Aki/Atg9atm1Aki
(involves: 129/Sv * C57BL/6)
|
abnormal autophagosome formation
|
J:155552
|
impaired autophagy
|
J:155552
|
Atg12tm1.1Jdth/Atg12tm1.1Jdth Tg(Pomc1-cre)1Gsb/0
(involves: C57BL/6 * FVB/N)
|
abnormal autophagy
|
J:232686
|
Atg16l1Gt(BC0122)Wtsi/Atg16l1Gt(BC0122)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired autophagy
|
J:141419
|
Atg16l1Gt(BC0122)Wtsi/Atg16l1Gt(BC0122)Wtsi Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129P2/OlaHsd * C57BL/6NCrj)
|
impaired autophagy
|
J:181308
|
Atg16l1Gt(XR0164)Wtsi/Atg16l1Gt(XR0164)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired autophagy
|
J:141419
|
Atg16l1tm1.1Mvlc/Atg16l1tm1.1Mvlc
(C57BL/6-Atg16l1tm1.1Mvlc)
|
impaired autophagy
|
J:206931
|
Atg16l1tm1Aki/Atg16l1tm1Aki
(involves: 129/Sv * C57BL/6)
|
abnormal autophagosome formation
|
J:141420
|
impaired autophagy
|
J:141420
|
Atg16l1tm1c(EUCOMM)Wtsi/Atg16l1tm1c(EUCOMM)Wtsi Tcrdtm1Mom/Tcrdtm1Mom Tg(Vil1-cre)997Gum/0
(involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N * SJL)
|
increased small intestinal crypt cell apoptosis
|
J:340266
|
Atg16l1tm1c(EUCOMM)Wtsi/Atg16l1tm1c(EUCOMM)Wtsi Tg(Itgax-cre)1-1Reiz/?
(involves: C57BL/6 * C57BL/6N * CBA)
|
cellular phenotype
|
J:221019
|
Atg16l1tm1c(EUCOMM)Wtsi/Atg16l1tm1c(EUCOMM)Wtsi Tg(Vil1-cre)997Gum/?
(involves: C57BL/6J * C57BL/6N * SJL)
|
abnormal autophagy
|
J:221019
|
Atg16l1tm1Kuv/Atg16l1tm1Kuv Tg(Vil1-cre)997Gum/0
(involves: C57BL/6 * SJL)
|
abnormal autophagy
|
J:206084
|
Atg16l1tm1Kuv/Atg16l1tm1Kuv Tg(Vil1-cre)997Gum/0
(B6.Cg-Atg16l1tm1Kuv Tg(Vil1-cre)997Gum)
|
increased enterocyte apoptosis
|
J:269933
|
Atg16l1tm1Kuv/Atg16l1tm1Kuv Tg(Vil1-cre)997Gum/0 Xbp1tm2Glm/Xbp1tm2Glm
(B6.Cg-Atg16l1tm1Kuv Xbp1tm2Glm Tg(Vil1-cre)997Gum)
|
increased enterocyte apoptosis
|
J:269933
|
Atg16l1tm2.1Mvlc/Atg16l1tm2.1Mvlc Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired autophagy
|
J:206931
|
Atictm1c(EUCOMM)Hmgu/Atictm1c(EUCOMM)Hmgu Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6J * C57BL/6N)
|
abnormal cell cycle
|
J:338121
|
decreased vascular smooth muscle cell proliferation
|
J:338121
|
Atictm1c(EUCOMM)Hmgu/Atictm1c(EUCOMM)Hmgu X/Tg(Myh11-icre/ERT2)1Soff
(involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N * FVB/N)
|
decreased vascular smooth muscle cell proliferation
|
J:338121
|
Atl1tm1.1Cbla/Atl1tm1.1Cbla
(C57BL/6-Atl1tm1.1Cbla)
|
abnormal endoplasmic reticulum morphology
|
J:334532
|
Atl1tm1.1Cbla/Atl1tm1.1Cbla Reep1Gt(OST398247)Tigm/Reep1Gt(OST398247)Tigm
(B6.Cg-Reep1Gt(OST398247)Tigm Atl1tm1.1Cbla)
|
abnormal endoplasmic reticulum morphology
|
J:334532
|
increased endoplasmic reticulum stress
|
J:334532
|
Atl1tm1.2Cbla/Atl1tm1.2Cbla Reep1Gt(OST398247)Tigm/Reep1Gt(OST398247)Tigm
(B6.Cg-Reep1Gt(OST398247)Tigm Atl1tm1.2Cbla)
|
abnormal endoplasmic reticulum morphology
|
J:334532
|
Atmm5Btlr/Atmm5Btlr
(C57BL/6J-Atmm5Btlr)
|
impaired macrophage phagocytosis
|
J:272824
|
Atmtm1.1Mmpl/Atmtm1.1Mmpl
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J)
|
abnormal DNA repair
|
J:226414
|
decreased cell proliferation
|
J:226414
|
decreased sensitivity to induced cell death
|
J:226414
|
Atmtm1Awb/Atmtm1Awb
(either: 129S6/SvEvTac-Atmtm1Awb or (involves: 129S6/SvEvTac * NIH Black Swiss))
|
abnormal cell cycle
|
J:34193
|
abnormal lysosome morphology
|
J:59933
|
absent oocytes
|
J:34193
|
azoospermia
|
J:34193
|
decreased fibroblast proliferation
|
J:34193
|
increased cellular sensitivity to gamma-irradiation
|
J:34193
|
oxidative stress
|
J:57115
|
Atmtm1Awb/Atmtm1Awb
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:103922
|
chromosome breakage
|
J:103922
|
Atmtm1Awb/Atmtm1Awb
(involves: 129S6/SvEvTac)
|
abnormal cell cycle checkpoint function
|
J:126920
|
abnormal chromosome morphology
|
J:170462
|
cellular phenotype
|
J:126186
|
spontaneous chromosome breakage
|
J:150435
|
Atmtm1Awb/Atmtm1Awb Nbntm2.1Jpt/Nbntm2.1Jpt
(involves: 129S6/SvEvTac * 129/Sv)
|
decreased cellular sensitivity to ionizing radiation
|
J:129762
|
Atmtm1Awb/Atmtm1Awb Pim1tm1Mjn/Pim1+
(involves: 129 * 129S6/SvEvTac * C57BL/6J)
|
cellular phenotype
|
J:194229
|
Atmtm1Awb/Atmtm1Awb Rad50tm2Jpt/Rad50tm2Jpt
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:103922
|
cellular phenotype
|
J:103922
|
chromosome breakage
|
J:103922
|
Atmtm1Bal/Atmtm1Bal
(involves: 129S4/SvJae)
|
abnormal cell cycle checkpoint function
|
J:42324
|
abnormal female meiosis
|
J:35914
|
absent oocytes
|
J:35914
|
arrest of male meiosis
|
J:35914
|
decreased fibroblast proliferation
|
J:42324
|
increased cellular sensitivity to gamma-irradiation
|
J:42324
|
Atmtm1Fwa/Atmtm1Fwa
(involves: 129S4/SvJae * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:61201
|
Atmtm1Fwa/Atmtm1Fwa
(involves: 129S4/SvJae)
|
chromosomal instability
|
J:191288
|
Atmtm1Fwa/Atmtm1Fwa H2axtm1Fwa/H2axtm1Fwa
(involves: 129S4/SvJae * 129S6/SvEvTac)
|
chromosomal instability
|
J:138190
|
increased cell death
|
J:138190
|
spontaneous chromosome breakage
|
J:138190
|
Atmtm1Led/Atmtm1Led
(involves: 129S6/SvEvTac * Black Swiss)
|
abnormal chromosome morphology
|
J:69726
|
azoospermia
|
J:36561
|
chromosome breakage
|
J:36561
|
increased cellular sensitivity to ionizing radiation
|
J:69726
|
Atmtm1Mfl/Atmtm1Mfl
(involves: 129T2/SvEms * C57BL/6J)
|
abnormal chromosome morphology
|
J:69726
|
abnormal oogenesis
|
J:69726
|
abnormal spermatocyte morphology
|
J:69726
|
decreased spermatid number
|
J:69726
|
increased cellular sensitivity to ionizing radiation
|
J:69726
|
Atmtm1Pmc/Atm+ Lig4tm1Icrf/Lig4tm1Icrf
(either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ))
|
increased neuron apoptosis
|
J:65540
|
Atmtm1Pmc/Atmtm1Pmc
(involves: 129X1/SvJ * C57BL/6)
|
decreased cellular sensitivity to ionizing radiation
|
J:47752
|
Atmtm1Pmc/Atmtm1Pmc
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:78491
|
decreased cellular sensitivity to gamma-irradiation
|
J:78491
|
Atmtm1Pmc/Atmtm1Pmc
(B6.Cg-Atmtm1Pmc)
|
abnormal cell cycle
|
J:222034
|
abnormal fat cell differentiation
|
J:222034
|
Atmtm1Pmc/Atmtm1Pmc Lig4tm1Icrf/Lig4+
(either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ))
|
increased neuron apoptosis
|
J:65540
|
Atmtm1Pmc/Atmtm1Pmc Lig4tm1Icrf/Lig4tm1Icrf
(either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ))
|
decreased neuron apoptosis
|
J:111068,
J:65540
|
Atmtm1Pmc/Atmtm1Pmc Lig4tm1Icrf/Lig4tm1Icrf
(involves: 129)
|
decreased cellular sensitivity to ionizing radiation
|
J:144172
|
Atmtm1Pmc/Atmtm1Pmc Trp73tm2Mak/Trp73tm2Mak
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cellular sensitivity to gamma-irradiation
|
J:157905
|
decreased thymocyte apoptosis
|
J:157905
|
Atmtm1Shzh/Atmtm2.1Fwa
(involves: 129S6/SvEvTac)
|
chromosomal instability
|
J:191288
|
Atmtm1Shzh/Atmtm2.1Fwa Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+
(involves: 129 * 129S6/SvEvTac)
|
chromosomal instability
|
J:191288
|
Atmtm2Pmc/Atmtm2Pmc Atrtm2Bal/Atrtm2Bal Tg(Nes-cre)1Kln/0
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal neuron apoptosis
|
J:181920
|
decreased cellular sensitivity to ionizing radiation
|
J:181920
|
Atmtm2Pmc/Atmtm2Pmc Meox2tm1(cre)Sor/Meox2+
(involves: 129S4/SvJaeSor * C57BL/6J)
|
decreased cellular sensitivity to ionizing radiation
|
J:181920
|
Atmtm2Pmc/Atmtm2Pmc Pnkptm1.1Pmc/Pnkptm1.1Pmc Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * C57BL/6 * SJL)
|
increased brain apoptosis
|
J:226703
|
Atmingpg6/Atmingpg6
(involves: BALB/cAnN * C3H/HeH)
|
abnormal motile primary cilium morphology
|
J:145068
|
Atmingpg6/Atmingpg6
(C3H.C-Atmingpg6)
|
abnormal embryonic neuroepithelium primary cilium morphology
|
J:217609
|
abnormal primary cilium morphology
|
J:217609
|
decreased embryonic cilium length
|
J:217609
|
Atmintm1.1Axbe/Atmintm1.1Axbe
(involves: BALB/c * C57BL/6)
|
abnormal cell physiology
|
J:167331
|
decreased cell proliferation
|
J:167331
|
early cellular replicative senescence
|
J:167331
|
Atmintm1.1Jhh/Atmintm1.1Jhh
(C57BL/6-Atmintm1.1Jhh)
|
abnormal base-excision repair
|
J:167544
|
cellular phenotype
|
J:167544
|
early cellular replicative senescence
|
J:167544
|
increased cellular sensitivity to hydrogen peroxide
|
J:167544
|
increased cellular sensitivity to methylmethanesulfonate
|
J:167544
|
Atmintm1.1Jhh/Atmintm1.1Jhh Cd79atm1(cre)Reth/Cd79a+
(B6.Cg-Cd79atm1(Cre)Reth Atmintm1.1Jhh)
|
increased B cell apoptosis
|
J:230105
|
Atmintm1.1Jhh/Atmintm1.1Jhh Cd79atm1(cre)Reth/Cd79a+ Tg(IghMyc)22Bri/0
(B6.Cg-Cd79atm1(Cre)Reth Atmintm1.1Jhh Tg(IghMyc)22Bri)
|
increased B cell apoptosis
|
J:230105
|
Atoh1tm3Hzo/Atoh1+ Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sortm1(Smo/EYFP)Amc
(involves: 129 * 129S7/SvEvBrd * 129X1/SvJ)
|
abnormal neuronal precursor proliferation
|
J:155047
|
Atoh1tm3Hzo/Atoh1tm1Hzo Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sortm1(Smo/EYFP)Amc
(involves: 129 * 129S7/SvEvBrd * 129X1/SvJ)
|
abnormal neuronal precursor proliferation
|
J:155047
|
Atoh1tm3Hzo/Atoh1tm3Hzo
(involves: 129S7/SvEvBrd)
|
decreased neuronal precursor proliferation
|
J:155047
|
Atoh7tm1(Neurod1)Whk/Atoh7tm2(Neurod4)Whk
(involves: 129S6/SvEvTac * C57BL/6)
|
increased retina apoptosis
|
J:141248
|
Atoh7tm1.1(Ascl1)Nlbr/Atoh7tm1.1(Ascl1)Nlbr Tg(Atoh7-cre)360Gla/0 Tg(CAG-Bgeo/GFP)21Lbe/0
(either: (involves: 129 * C57BL/6 * FVB/N * SJL) or (involves: 129 * C57BL/6 * CD-1 * FVB/N * SJL))
|
abnormal cell cycle
|
J:203642
|
increased retina apoptosis
|
J:203642
|
Atoh7tm1Gan/Atoh7tm1(Neurod1)Whk
(involves: 129S6/SvEvTac * C57BL/6)
|
increased retina apoptosis
|
J:141248
|
Atoh7tm1Gan/Atoh7tm1Gan
(B6.Cg-Atoh7tm1Gan)
|
increased retina apoptosis
|
J:135827
|
Atoh7tm1Gan/Atoh7tm1Gan Pou4f2tm1Nat/Pou4f2tm1Nat
(B6.Cg-Pou4f2tm1Nat Atoh7tm1Gan)
|
increased retina apoptosis
|
J:135827
|
Atoh7tm1Gla/Atoh7tm1Gla
(either: (involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
abnormal cell cycle
|
J:110600
|
Atox1Gt(IRESBetageo)3Pgr/Atox1Gt(IRESBetageo)3Pgr
(B6.129(Cg)-Atox1Gt(IRESBetageo)3Pgr/Mmucd)
|
maternal effect
|
J:74249
|
Atp1a4tm1Blac/Atp1a4tm1Blac
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased hyperactivated sperm motility
|
J:203477
|
kinked sperm flagellum
|
J:203477
|
Atp1a4tm1Itl/Atp1a4+
(involves: 129S6/SvEvTac * C57BL/6)
|
asthenozoospermia
|
J:169420
|
Atp1a4tm1Itl/Atp1a4tm1Itl
(involves: 129S6/SvEvTac * C57BL/6)
|
asthenozoospermia
|
J:169420
|
kinked sperm flagellum
|
J:169420
|
teratozoospermia
|
J:169420
|
Atp1b2tm1(Atp1b1)Mtg/Atp1b2tm1(Atp1b1)Mtg
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased retina apoptosis
|
J:50902
|
Atp2a2tm1.1Raco/Atp2a2+
(C57BL/6J-Atp2a2tm1.1Raco/Raco)
|
abnormal vascular endothelial cell migration
|
J:216004
|
Atp2a2tm1Fwuy/Atp2a2tm1Fwuy
(involves: 129S1/Sv * 129X1/SvJ * Swiss)
|
cardiac interstitial fibrosis
|
J:111247
|
Atp2a2tm1Ges/Atp2a2+
(involves: 129X1/SvJ)
|
abnormal osteoclast differentiation
|
J:198051
|
Atp2b2jog/Atp2b2jog
(involves: C57BL/6 * DSO)
|
abnormal cell death
|
J:111625
|
Atp2b2wri/Atp2b2wri
(involves: BALB/cAnN)
|
abnormal Purkinje cell differentiation
|
J:13355
|
Atp2b4tm1Ges/Atp2b4tm1Ges
(BKSW.129X1-Atp2b4tm1Ges)
|
asthenozoospermia
|
J:91844
|
Atp2b4tm1Ksch/Atp2b4tm1Ksch
(involves: 129P2/OlaHsd * C57BL/6)
|
asthenozoospermia
|
J:121031
|
Atp2c1tm1Ges/Atp2c1tm1Ges
(involves: 129X1/SvJ * Black Swiss)
|
abnormal cell morphology
|
J:124662
|
abnormal endoplasmic reticulum morphology
|
J:124662
|
abnormal Golgi apparatus morphology
|
J:124662
|
increased head mesenchyme apoptosis
|
J:124662
|
increased neural tube apoptosis
|
J:124662
|
Atp5if1em1Jpy/Atp5if1em1Jpy
(C57BL/6J-Atp5if1em1Jpy)
|
abnormal mitochondrial matrix morphology
|
J:313048
|
abnormal mitophagy
|
J:313048
|
decreased enterocyte apoptosis
|
J:313048
|
decreased mitochondrial size
|
J:313048
|
Atp6ap2em1Nira/Y
(C57BL/6J-Atp6ap2em1Nira)
|
cellular phenotype
|
J:324587
|
Atp6ap2tm1.1Aich/Y Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * C57BL/6J * CBA/J)
|
impaired autophagy
|
J:274386
|
Atp6ap2tm1.1Aich/Atp6ap2tm1.1Aich Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * C57BL/6J * CBA/J)
|
impaired autophagy
|
J:274386
|
Atp6ap2tm1.1Ics/Y
(involves: C57BL/6 * C57BL/6N)
|
impaired autophagy
|
J:232697
|
Atp6ap2tm1.1Ics/Y Tg(NPHS2-cre)295Lbh/0
(involves: C57BL/6 * C57BL/6N * SJL)
|
abnormal cell cytoskeleton morphology
|
J:232697
|
impaired autophagy
|
J:232697
|
increased podocyte apoptosis
|
J:232697
|
Atp6v0a1em2Hisa/Atp6v0a1em2Hisa
(involves: ICR)
|
abnormal lysosome morphology
|
J:305201
|
impaired autophagy
|
J:305201
|
increased neuron apoptosis
|
J:305201
|
Atp6v0d1em1Nju/Atp6v0d1em1Nju Tg(Adipoq-cre)1Evdr/0
(involves: FVB/NJ)
|
increased fibroblast proliferation
|
J:346448
|
Atp6v0d2tm1Ywc/Atp6v0d2tm1Ywc
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:117744
|
Atp6v1hem1Xhd/Atp6v1h+
(involves: C57BL/6)
|
abnormal osteoclast differentiation
|
J:239439
|
Atp7aMo-blo/Y
(B6.Cg-Atp7aMo-blo/J)
|
oxidative stress
|
J:105736
|
Atp7aMo-blo/?
(Not Specified)
|
abnormal cell morphology
|
J:5880
|
Atp7aMo-brJ/Y Mt1tm1Bri/Mt1tm1Bri Mt2tm1Bri/Mt2tm1Bri
(involves: 129S7/SvEvBrd * C3H/HeJ * C57BL/6J)
|
increased sensitivity to induced cell death
|
J:33276
|
Atp7aMo-brJ/Atp7a+ Mt1tm1Bri/Mt1tm1Bri Mt2tm1Bri/Mt2tm1Bri
(involves: 129S7/SvEvBrd * C3H/HeJ)
|
increased sensitivity to induced cell death
|
J:33276
|
Atp7aMo-ms/Y
(Not Specified)
|
increased neuron apoptosis
|
J:157286
|
Atp7aMo-Tohm/Atp7a+
(B6.Cg-Atp7aMo-Tohm)
|
increased brain apoptosis
|
J:105797
|
Atp7aMo-vbr/Y
(Not Specified)
|
abnormal mitochondrial physiology
|
J:44695
|
Atp7atm1.2Mlke/Y
(involves: C57BL/6J)
|
abnormal cell physiology
|
J:266704
|
Atp7btx-J/Atp7btx-J
(C3H/HeJ-Atp7btx-J/J)
|
maternal effect
|
J:24233
|
Atp7btx/Atp7btx
(DL-Atp7btx)
|
maternal effect
|
J:66749
|
Atp11atm1c(KOMP)Wtsi/Atp11atm1c(KOMP)Wtsi Myf5tm3(cre)Sor/Myf5+
(involves: 129S4/SvJaeSor * C57BL/6JJcl * C57BL/6N)
|
abnormal myoblast differentiation
|
J:262981
|
Atp13a2tm1.2Wtd/Atp13a2tm1.2Wtd
(involves: 129 * C57BL/6)
|
abnormal lysosome morphology
|
J:221680
|
abnormal lysosome physiology
|
J:221680
|
impaired autophagy
|
J:221680
|
lysosomal protein accumulation
|
J:221680
|
Atp13a2tm1.2Wtd/Atp13a2tm1.2Wtd Sncatm1Wtd/Sncatm1Wtd
(involves: 129 * C57BL/6)
|
abnormal lysosome morphology
|
J:221680
|
Atp13a2tm1.2Wtd/Atp13a2tm1.2Wtd Tg(Prnp-SNCA*A53T)83Vle/0
(involves: 129 * C3H * C57BL/6)
|
abnormal lysosome morphology
|
J:221680
|
Atp13a3em2H/Atp13a3+
(C57BL/6NTac-Atp13a3em2H/H)
|
cardiac interstitial fibrosis
|
J:358006
|
Atpaf1em1Cya/Atpaf1em1Cya
(involves: C57BL/6N)
|
abnormal cellular respiration
|
J:347150
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:347150
|
abnormal mitochondrial crista morphology
|
J:347150
|
abnormal mitochondrial physiology
|
J:347150
|
abnormal myocardial fiber mitochondrial morphology
|
J:347150
|
abnormal oxidative phosphorylation
|
J:347150
|
decreased mitochondrial size
|
J:347150
|
dilated mitochondrion
|
J:347150
|
impaired autophagy
|
J:347150
|
increased myocardial fiber apoptosis
|
J:347150
|
oxidative stress
|
J:347150
|
Atrtm1Bal/Atrtm2Bal Ndor1Tg(UBC-cre/ERT2)1Ejb/0
(involves: 129S/SvEv * 129S2/SvPas * C57BL/6)
|
decreased cell proliferation
|
J:123200
|
Atrtm1Ofc/Atrtm1Ofc
(Not Specified)
|
abnormal cell cycle
|
J:151542
|
abnormal DNA replication
|
J:151542
|
abnormal oogenesis
|
J:151542
|
absent oocytes
|
J:151542
|
early cellular replicative senescence
|
J:151542
|
increased apoptosis
|
J:151542
|
increased cellular sensitivity to methylmethanesulfonate
|
J:151542
|
increased cellular sensitivity to ultraviolet irradiation
|
J:151542
|
increased fibroblast apoptosis
|
J:151542
|
spontaneous chromosome breakage
|
J:151542
|
Atrtm1Ofc/Atrtm1Ofc
(involves: 129 * C57BL/6)
|
abnormal female meiosis
|
J:307570
|
decreased granulosa cell proliferation
|
J:307570
|
increased granulosa cell apoptosis
|
J:307570
|
increased granulosa cell proliferation
|
J:307570
|
Atrtm1Ofc/Atrtm1Ofc Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas)
|
abnormal DNA replication
|
J:151542
|
increased embryonic tissue cell apoptosis
|
J:151542
|
Atrtm1Twgl/Atr+
(involves: 129S6/SvEvTac * C57BL/6J)
|
decreased mitotic index
|
J:150723
|
induced chromosome breakage
|
J:150723
|
Atrtm1Twgl/Atrtm1Twgl
(involves: 129S6/SvEvTac * C57BL/6J)
|
decreased mitotic index
|
J:150723
|
induced chromosome breakage
|
J:150723
|
Atrtm2Bal/Atrtm2Bal Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
abnormal neuron proliferation
|
J:181920
|
Atrtm2Bal/Atrtm2Bal Tg(Nes-cre)1Kln/0
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal neuron proliferation
|
J:181920
|
decreased cerebellar granule cell precursor proliferation
|
J:181920
|
increased neuron apoptosis
|
J:181920
|
Atrtm2Bal/Atrtm2Bal Trp53tm1Tyj/Trp53tm1Tyj Tg(Nes-cre)1Kln/0
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal neuron apoptosis
|
J:181920
|
abnormal neuron proliferation
|
J:181920
|
Atriptm1.1Pof/Atriptm1.1Pof Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:299031
|
abnormal mitosis
|
J:299031
|
increased lens epithelium apoptosis
|
J:299031
|
Atriptm1.1Pof/Atriptm1.1Pof Tg(Nes-cre)1Kln/0 Trp53tm1Brn/Trp53tm1Brn
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:299031
|
abnormal mitosis
|
J:299031
|
Atriptm1.1Pof/Atriptm1.1Pof Tg(Pax6-cre,GFP)2Pgr/0
(involves: 129P2/OlaHsd * C57BL/6)
|
increased retina apoptosis
|
J:297493
|
Atrxtm1Rjg/Y Tg(Gata1-cre)1Sho/0
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
decreased cell proliferation
|
J:115836
|
Atrxtm1Rjg/Atrx+ Tg(Gata1-cre)1Sho/0
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
abnormal imprinting
|
J:115836
|
Atxn2lem1Aub/Atxn2lem1Aub
(Not Specified)
|
abnormal cell morphology
|
J:294770
|
increased neuron apoptosis
|
J:294770
|
Atxn7l3tm1(KOMP)Wtsi/Atxn7l3tm1(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal cell physiology
|
J:213770
|
AU040320tm1b(EUCOMM)Wtsi/AU040320tm1b(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal acrosome assembly
|
J:264829
|
abnormal acrosome morphology
|
J:264829
|
abnormal proacrosomal vesicle fusion
|
J:264829
|
abnormal sperm midpiece morphology
|
J:264829
|
abnormal sperm mitochondrial morphology
|
J:264829
|
abnormal sperm mitochondrial sheath morphology
|
J:264829
|
abnormal sperm nucleus morphology
|
J:264829
|
absent acrosome
|
J:264829
|
asthenozoospermia
|
J:264829
|
coiled sperm flagellum
|
J:264829
|
globozoospermia
|
J:264829
|
immotile sperm
|
J:264829
|
oligozoospermia
|
J:264829
|
small sperm head
|
J:264829
|
AurkaGt(XQ0149)Wtsi/Aurka+
(involves: 129P2/OlaHsd * C57BL/6)
|
aneuploidy
|
J:143099
|
chromosomal instability
|
J:143099
|
AurkaGt(XQ0149)Wtsi/AurkaGt(XQ0149)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal mitosis
|
J:143099
|
abnormal mitotic spindle morphology
|
J:143099
|
Aurkatm1.1Tvd/Aurkatm1.1Tvd Ccn6tm1(cre)Mawa/Ccn6+
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J)
|
abnormal sperm head morphology
|
J:321647
|
abnormal sperm midpiece morphology
|
J:321647
|
abnormal sperm motility
|
J:321647
|
increased male germ cell apoptosis
|
J:321647
|
increased sperm progressive motility
|
J:321647
|
kinked sperm flagellum
|
J:321647
|
multiflagellated sperm
|
J:321647
|
oligozoospermia
|
J:321647
|
teratozoospermia
|
J:321647
|
Aurkatm1.1Tvd/Aurkatm1.1Tvd Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129 * 129P2/OlaHsd * C57BL/6J)
|
abnormal mitosis
|
J:145744
|
increased apoptosis
|
J:145744
|
increased mitotic index
|
J:145744
|
Aurkatm1.1Tvd/Aurkatm1.1Tvd Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sortm1Sor
(involves: 129 * 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:145744
|
abnormal chromosome number
|
J:145744
|
abnormal mitosis
|
J:145744
|
decreased cell proliferation
|
J:145744
|
increased mitotic index
|
J:145744
|
Aurkatm1.1Tvd/Aurkatm1.1Tvd Tg(Ddx4-cre)1Dcas/0
(involves: 129P2/OlaHsd * C57BL/6J * FVB)
|
absent germ cells
|
J:321647
|
azoospermia
|
J:321647
|
Aurkatm1.2Sbsn/Aurkatm1.2Sbsn
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:198479
|
abnormal mitosis
|
J:198479
|
abnormal mitotic spindle morphology
|
J:198479
|
Aurkatm1.2Tvd/Aurkatm1.2Tvd
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal mitotic spindle morphology
|
J:145744
|
increased mitotic index
|
J:145744
|
Aurkatm1c(EUCOMM)Hmgu/Aurkatm1c(EUCOMM)Hmgu Tg(Gdf9-icre)5092Coo/0
(involves: C57BL/6 * C57BL/6J * C57BL/6N)
|
abnormal female meiosis I arrest
|
J:307094
|
abnormal meiotic spindle morphology
|
J:307094
|
Aurkbtm1.1Mama/Aurkbtm1.1Mama
(involves: 129/Sv * C57BL/6 * CD-1 * SJL)
|
abnormal cell morphology
|
J:173575
|
abnormal cell nucleus morphology
|
J:173575
|
abnormal mitosis
|
J:173575
|
abnormal mitotic spindle morphology
|
J:173575
|
increased cell nucleus count
|
J:173575
|
increased fibroblast apoptosis
|
J:173575
|
polyploidy
|
J:173575
|
Aurkbtm1.2Mama/Aurkb+
(involves: 129/Sv * BALB/cJ * C57BL/6 * CD-1 * SJL)
|
oligozoospermia
|
J:173575
|
Aurkbtm1.2Mama/Aurkbtm2.2Mama
(involves: 129/Sv * BALB/cJ * C57BL/6 * CD-1 * SJL)
|
abnormal mitosis
|
J:173575
|
abnormal mitotic spindle morphology
|
J:173575
|
increased embryonic tissue cell apoptosis
|
J:173575
|
polyploidy
|
J:173575
|
Aurkctm1Lex/Aurkctm1Lex
(B6.129S-Aurkctm1Lex)
|
abnormal acrosome morphology
|
J:142947
|
abnormal sperm head morphology
|
J:142947
|
abnormal sperm nucleus morphology
|
J:142947
|
detached acrosome
|
J:142947
|
Auts2tm1.1Mhos/Auts2tm1.1Mhos
(involves: C57BL/6 * C57BL/6N)
|
abnormal axon extension
|
J:243531
|
abnormal neuronal migration
|
J:243531
|
Auts2tm1.2Mhos/Auts2+
(involves: C57BL/6 * C57BL/6N)
|
abnormal neuronal migration
|
J:243531
|
Auts2tm1.2Mhos/Auts2tm1.2Mhos
(involves: C57BL/6 * C57BL/6N)
|
abnormal axon extension
|
J:243531
|
abnormal neuronal migration
|
J:243531
|
Auts2tm1Mhos/Auts2+
(C57BL/6N-Auts2tm1Mhos)
|
abnormal neuronal migration
|
J:243531
|
Auts2tm1Mhos/Auts2tm1Mhos
(C57BL/6N-Auts2tm1Mhos)
|
abnormal neuronal migration
|
J:243531
|
Aventm1.1Zrng/Aventm1.1Zrng
(involves: 129 * C57BL/6)
|
abnormal apoptosis
|
J:82809
|
Aviltm2(cre)Fawa/Avil+ Pik3c3tm1Fawa/Pik3c3tm1Fawa
(involves: 129P2/OlaHsd)
|
increased neuron apoptosis
|
J:160568
|
Aviltm2(cre)Fawa/Avil+ Prdm12tm1.1Ejbd/Prdm12tm1.1Ejbd
(involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N)
|
increased neuron apoptosis
|
J:283226
|
Aviltm2(cre)Fawa/Aviltm2(cre)Fawa
(B6J.129P2-Aviltm2(cre)Fawa)
|
abnormal axon extension
|
J:265529
|
Axd/Axd
(involves: BALB/c * BALB/cAnNCrl * C3H/HeN * C57BL/6)
|
decreased cell proliferation
|
J:170759
|
Axdnd1em1Ktmr/Axdnd1em1Ktmr
(C57BL/6N-Axdnd1em1Ktmr)
|
abnormal manchette morphology
|
J:324162
|
abnormal sperm head morphology
|
J:324162
|
increased male germ cell apoptosis
|
J:324162
|
oligozoospermia
|
J:324162
|
Axin1Fu/Axin1+
(Not Specified)
|
maternal effect
|
J:12953
|
Axin1Fu/Axin1+
(involves: C57BL/6J * CBA/Lac)
|
paternal imprinting
|
J:133043
|
Axin1Fu/Axin1+
(129P4.Cg-Axin1Fu/J)
|
genetic imprinting
|
J:82396
|
maternal imprinting
|
J:82396
|
paternal imprinting
|
J:82396
|
Axin1Fu/Axin1+
(involves: 129/Rr * C3H/He * C57BL/6J)
|
genetic imprinting
|
J:6577
|
paternal imprinting
|
J:6577
|
Axin1Fu/Axin1+
(involves: 129/Rr * C3H/He * C57BL/6J * wild)
|
genetic imprinting
|
J:6577
|
Axin1Fu/Axin1Fu
(Not Specified)
|
maternal effect
|
J:12953
|
Axin2tm1.1(cre/ERT2/tdTomato)Eem/Axin2+ Ctnnb1tm2Kem/Ctnnb1tm2Kem
(involves: 129S2/SvPas * C57BL/6)
|
decreased cell proliferation
|
J:204142
|
Axin2tm1Wbm/Axin2tm1Wbm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoblast physiology
|
J:98523
|
enhanced osteoblast differentiation
|
J:98523
|
increased osteoblast proliferation
|
J:98523
|
Axltm1Grl/Axltm1Grl Mertktm1Grl/Mertktm1Grl Tyro3tm1Grl/Tyro3tm1Grl
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
azoospermia
|
J:54681
|
increased apoptosis
|
J:54681
|
increased B cell proliferation
|
J:70420
|
increased brain apoptosis
|
J:54681
|
increased granulosa cell apoptosis
|
J:54681
|
increased splenocyte apoptosis
|
J:54681
|
increased T cell proliferation
|
J:70420
|
Axltm1Grl/Axltm1Grl Tyro3tm1Grl/Tyro3tm1Grl
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
impaired neuronal migration
|
J:141251
|
increased apoptosis
|
J:141251
|
increased neuron apoptosis
|
J:141251
|
Azi2tm1Aki/Azi2tm1Aki
(Not Specified)
|
abnormal dendritic cell differentiation
|
J:204786
|
b2b227Clo/b2b227Clo
(C57BL/6J-b2b227Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
immotile respiratory cilia
|
J:175213
|
b2b635Clo/b2b635Clo
(C57BL/6J-b2b635Clo)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:242757
|
b2b1146Clo/b2b1146Clo
(C57BL/6J-b2b1146Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
immotile respiratory cilia
|
J:175213
|
b2b1468Clo/b2b1468Clo
(C57BL/6J-b2b1468Clo)
|
immotile respiratory cilia
|
J:175213
|
b2b1700Clo/b2b1700Clo
(C57BL/6J-b2b1700Clo)
|
immotile respiratory cilia
|
J:175213
|
b2b1929Clo/b2b1929Clo
(C57BL/6J-b2b1929Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
b2b2059Clo/b2b2059Clo
(C57BL/6J-b2b2059Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
B2mtm1Jae/B2mtm1Jae Rr94tm3.2Litt/Rr94tm3.2Litt
(involves: 129P2/OlaHsd * 129S2/SvPas * FVB/N)
|
increased T cell proliferation
|
J:158962
|
B2mtm1Unc/B2mtm1Unc H2-Ab1b-tm1Doi/H2-Ab1b-tm1Doi
(involves: 129P2/OlaHsd * 129S2/SvPas)
|
abnormal neuron proliferation
|
J:170591
|
B3gat3tm1Hkit/B3gat3tm1Hkit
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal mitotic cytokinesis
|
J:225032
|
B3gnt2Gt(KST308)Byg/B3gnt2Gt(KST308)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased neuron apoptosis
|
J:97372
|
B3gnt2Gt(OST237555)Lex/B3gnt2Gt(OST237555)Lex
(involves: 129S5/SvEvBrd * C57BL/6N)
|
increased T cell proliferation
|
J:125556
|
B3gnt6tm1Lx/B3gnt6tm1Lx
(involves: 129S1/Sv * C57BL/6J)
|
abnormal enterocyte proliferation
|
J:123826
|
B4galnt1tm1Rlp/B4galnt1tm1Rlp St3gal5tm1Rlp/St3gal5tm1Rlp
(involves: 129S6/SvEvTac * C57BL/6)
|
increased brain apoptosis
|
J:96830
|
B4galnt2a/B4galnt2b Msh2tm1Htr/Msh2tm1Htr
(involves: 129P2/OlaHsd * BALB/c * SWR)
|
decreased enterocyte apoptosis
|
J:54082
|
B4galt1tm1Shur/B4galt1tm1Shur
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal sperm motility
|
J:43773
|
B4galt1tm1Yiw/B4galt1tm1Yiw
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
impaired macrophage chemotaxis
|
J:89125
|
increased mitotic index
|
J:106669
|
B4galt6tm1Kfk/B4galt6tm1Kfk
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal cell physiology
|
J:260410
|
B4gat1m1Ddg/B4gat1m1Ddg
(involves: C3H/He * C57BL/6)
|
abnormal axon fasciculation
|
J:194150
|
abnormal axon guidance
|
J:194150
|
B4gat1m1Ddg/B4gat1tm1(KOMP)Vlcg
(involves: C3H/He * C57BL/6 * C57BL/6NTac)
|
abnormal axon fasciculation
|
J:194150
|
abnormal axon guidance
|
J:194150
|
abnormal basement membrane morphology
|
J:194150
|
abnormal neuronal migration
|
J:194150
|
radial glial endfoot detachment
|
J:194150
|
B4gat1tm1Mifu/B4gat1tm1Mifu
(B6.Cg-B4gat1tm1Mifu)
|
impaired leukocyte tethering or rolling
|
J:120722
|
B4gat1tm1Mifu/B4gat1tm1Mifu Gcnt1tm1Jxm/Gcnt1tm1Jxm
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:120722
|
impaired leukocyte tethering or rolling
|
J:120722
|
B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
decreased embryonic cilium length
|
J:178421
|
decreased embryonic cilium number
|
J:178421
|
B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi
(involves: C57BL/6N * CD-1)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:178421
|
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv Tg(Cd4-cre)1Cwi/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2)
|
increased T cell proliferation
|
J:123547
|
B9d2/Tgfb1tm1Flv/Tgfb1tm2Flv Tnfrsf4tm2(cre)Nik/Tnfrsf4+
(involves: 129S6/SvEvTac * 129X1/SvJ)
|
abnormal enterocyte proliferation
|
J:169839
|
B9d2/Tgfb1tm1Flv/B9d2+ Tnfrsf4tm2(cre)Nik/Tnfrsf4+
(involves: 129S6/SvEvTac * 129X1/SvJ)
|
abnormal enterocyte proliferation
|
J:169839
|
Babam1Gt(IST11207B9)Tigm/Babam1Gt(IST11207B9)Tigm
(involves: C57BL/6N)
|
abnormal cell cycle
|
J:223526
|
increased hematopoietic stem cell proliferation
|
J:223526
|
Babam2tm1b(EUCOMM)Wtsi/Babam2tm1b(EUCOMM)Wtsi
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal DNA repair
|
J:235690
|
decreased fibroblast proliferation
|
J:235690
|
early cellular replicative senescence
|
J:235690
|
increased fibroblast apoptosis
|
J:235690
|
Bace1tm1Nn/Bace1tm1Nn
(Not Specified)
|
abnormal cell physiology
|
J:100272
|
Bace2tm1Bdes/Bace2tm1Bdes
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:100925
|
Bach1tm1Igar/Bach1tm1Igar
(B6.129P2-Bach1tm1Igar)
|
decreased cardiomyocyte apoptosis
|
J:123370
|
Badtm1Meg/Badtm1Meg
(involves: 129S4/SvJae)
|
abnormal apoptosis
|
J:88139
|
increased pancreatic beta cell apoptosis
|
J:133563
|
Badtm1Sjk/Badtm1Sjk
(either: 129X1/SvJ or (involves: 129X1/SvJ * C57BL/6))
|
abnormal apoptosis
|
J:84987
|
increased cellular sensitivity to gamma-irradiation
|
J:84987
|
multinucleated giant male germ cells
|
J:84987
|
Bag3Gt(OST16086)Lex/Bag3Gt(OST16086)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:112361
|
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1.1Chen Tg(Myhca-cre)1Abel/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * FVB/N)
|
impaired autophagy
|
J:246352
|
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu Tg(CAG-EGFP/Map1lc3b)53Nmz/0 Tg(Myhca-cre)1Abel/0
(involves: C57BL/6 * C57BL/6N * C57BL/6NCrlj * DBA/2 * FVB/N)
|
impaired autophagy
|
J:246352
|
Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu Tg(Myhca-cre)1Abel/0
(involves: C57BL/6N * FVB/N)
|
abnormal autophagosome formation
|
J:246352
|
impaired autophagy
|
J:246352
|
Bag6tm1Pmc/Bag6tm1Pmc
(involves: 129S1/Sv * C57BL/6)
|
decreased susceptibility to neuronal excitotoxicity
|
J:119857
|
increased kidney apoptosis
|
J:119857
|
increased kidney cell proliferation
|
J:119857
|
Bak1tm1Thsn/Bak1tm1Thsn Baxtm1Sjk/Baxtm1Sjk
(involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:66872
|
Bak1tm1Thsn/Bak1tm1Thsn Baxtm2Sjk/Baxtm2Sjk Tg(Lck-cre)1Cwi/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
decreased thymocyte apoptosis
|
J:220951
|
Bank1tm1Kuro/Bank1tm1Kuro
(Not Specified)
|
increased B cell proliferation
|
J:113321
|
Bap1em1Test/Bap1+
(involves: FVB)
|
abnormal DNA methylation
|
J:213725
|
abnormal epigenetic regulation of gene expression
|
J:213725
|
Bard1tm1.1Rjbr/Bard1tm1.1Rjbr
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal DNA replication
|
J:269011
|
decreased male germ cell number
|
J:269011
|
increased cellular sensitivity to DNA damaging agents
|
J:269011
|
Bard1tm1Thl/Bard1tm1Thl Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S1/Sv * 129S2/SvPas)
|
chromosome breakage
|
J:84329
|
Bard1tm2.1Rjbr/Bard1tm2.1Rjbr
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal DNA replication
|
J:269011
|
decreased male germ cell number
|
J:269011
|
increased cellular sensitivity to DNA damaging agents
|
J:269011
|
Barx1tm1Shiv/Barx1tm1Shiv
(either: B6.Cg-Barx1tm1Shiv or 129S.Cg-Barx1tm1Shiv or (involves: CD-1))
|
decreased cell proliferation
|
J:180393
|
increased cell proliferation
|
J:180393
|
Basp1tm1Crni/Basp1tm1Crni
(Not Specified)
|
abnormal axon extension
|
J:63023
|
Batf3tm1Kmm/Batf3tm1Kmm
(involves: 129S6/SvEvTac * BALB/cJ)
|
abnormal dendritic cell differentiation
|
J:141064
|
Baxtm1Dlo/Baxtm1Dlo
(involves: 129P2/OlaHsd)
|
decreased apoptosis
|
J:66953
|
decreased neuron apoptosis
|
J:39573,
J:66953
|
Baxtm1Dlo/Baxtm1Dlo Bcl2l1tm1Dlo/Bcl2l1tm1Dlo
(involves: 129P2/OlaHsd)
|
decreased neuron apoptosis
|
J:39573
|
Baxtm1Ofxa/Baxtm1Ofxa
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased neuron apoptosis
|
J:61471
|
Baxtm1Sjk/Bax+ Bcl2l1tm1Mam/Bcl2l1tm1Mam
(involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)
|
decreased male germ cell number
|
J:63161
|
Baxtm1Sjk/Bax+ KitlSl/KitlSl Tg(Pou5f1-GFP)1Scho/?
(involves: 129X1/SvJ * C3H * CD-1 * FVB)
|
abnormal primordial germ cell proliferation
|
J:115283
|
Baxtm1Sjk/Bax+ Nanos2tm1Ysa/Nanos2tm1Ysa
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal male germ cell apoptosis
|
J:132711
|
azoospermia
|
J:132711
|
Baxtm1Sjk/Baxtm1Sjk
(involves: 129X1/SvJ)
|
azoospermia
|
J:29253
|
decreased neuron apoptosis
|
J:35372
|
increased male germ cell apoptosis
|
J:29253
|
Baxtm1Sjk/Baxtm1Sjk
(B6.129X1-Baxtm1Sjk/J)
|
arrest of male meiosis
|
J:103605
|
azoospermia
|
J:103605
|
Baxtm1Sjk/Baxtm1Sjk
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6)
|
abnormal axon extension
|
J:100886
|
Baxtm1Sjk/Baxtm1Sjk Bcl2l1tm1Mam/Bcl2l1tm1Mam
(involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6)
|
azoospermia
|
J:63161
|
Baxtm1Sjk/Baxtm1Sjk Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast
(B6.129-Bcl2l11tm1.1Ast Baxtm1Sjk)
|
arrest of male meiosis
|
J:103605
|
azoospermia
|
J:103605
|
Baxtm1Sjk/Baxtm1Sjk KitlSl/KitlSl Tg(Pou5f1-GFP)1Scho/?
(involves: 129X1/SvJ * C3H * CD-1 * FVB)
|
abnormal primordial germ cell migration
|
J:115283
|
abnormal primordial germ cell proliferation
|
J:115283
|
Baxtm1Sjk/Baxtm1Sjk Nanos2tm1Ysa/Nanos2tm1Ysa
(involves: 129S1/Sv * 129X1/SvJ)
|
azoospermia
|
J:132711
|
Baxtm1Sjk/Baxtm1Sjk Ror2Y324C/Ror2Y324C
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal primordial germ cell migration
|
J:179805
|
abnormal primordial germ cell morphology
|
J:179805
|
decreased primordial germ cell number
|
J:179805
|
Baxtm1Sjk/Baxtm1Sjk Tg(SOD1*G93A)1Gur/0
(involves: 129X1/SvJ * C57BL/6 * SJL)
|
abnormal mitochondrial morphology
|
J:111890
|
Baxtm1Sjk/Baxtm1Sjk Wnt4tm1Amc/Wnt4tm3(EGFP/cre)Amc
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal oogenesis
|
J:203797
|
Baz1atm1.1Sky/Baz1atm1.1Sky
(involves: C57BL/6J * FVB/NJ)
|
abnormal sperm annulus morphology
|
J:223044
|
abnormal sperm flagellum morphology
|
J:223044
|
abnormal sperm head morphology
|
J:223044
|
abnormal sperm midpiece morphology
|
J:223044
|
abnormal spermatid morphology
|
J:223044
|
asthenozoospermia
|
J:223044
|
biflagellated sperm
|
J:223044
|
cellular phenotype
|
J:223044
|
coiled sperm flagellum
|
J:223044
|
increased testis apoptosis
|
J:223044
|
multinucleated giant male germ cells
|
J:223044
|
oligozoospermia
|
J:223044
|
teratozoospermia
|
J:223044
|
Baz1atm1.1Sky/Baz1atm1.1Sky Pim1tm1Mjn/Pim1+
(involves: 129 * C57BL/6J * FVB/NJ)
|
cellular phenotype
|
J:223044
|
Baz1btm1Ska/Baz1btm1Ska
(involves: C57BL/6 * CBA)
|
abnormal double-strand DNA break repair
|
J:149990
|
cellular phenotype
|
J:149990
|
Bbc3tm1Ast/Bbc3tm1Ast
(C57BL/6-Bbc3tm1Ast)
|
decreased cellular sensitivity to gamma-irradiation
|
J:86466
|
decreased sensitivity to induced cell death
|
J:86466
|
Bbc3tm1Gpz/Bbc3tm1Gpz
(involves: 129P2/OlaHsd)
|
abnormal cell death
|
J:115660
|
decreased apoptosis
|
J:116287
|
decreased cellular sensitivity to gamma-irradiation
|
J:115660
|
Bblntm1(KOMP)Wtsi/Bbln+
(involves: C57BL/6N)
|
abnormal osteoclast differentiation
|
J:296689
|
Bblntm1(KOMP)Wtsi/Bblntm1(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal osteoclast differentiation
|
J:296689
|
Bbof1em1Liwe/Bbof1em1Liwe
(C57BL/6J-Bbof1em1Liwe)
|
abnormal motile cilium physiology
|
J:339669
|
abnormal sperm axoneme morphology
|
J:339669
|
asthenozoospermia
|
J:339669
|
decreased sperm progressive motility
|
J:339669
|
Bbs1Gt1Nk/Bbs1Gt1Nk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal olfactory epithelium cilium morphology
|
J:92950
|
Bbs1tm1Vcs/Bbs1tm1Vcs
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal ependyma motile cilium morphology
|
J:128532
|
abnormal neuronal precursor proliferation
|
J:194096
|
absent sperm flagellum
|
J:128532
|
increased neuron apoptosis
|
J:194096
|
Bbs1tm2Vcs/Bbs1tm2Vcs Tg(Pdgfra-cre)1Clc/0
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased neuronal precursor proliferation
|
J:194096
|
increased neuron apoptosis
|
J:194096
|
Bbs2tm1.1Huss/Bbs2tm1.1Huss
(involves: 129S6/SvEv * C57BL/6)
|
abnormal olfactory epithelium cilium morphology
|
J:296033
|
abnormal primary cilium morphology
|
J:296033
|
Bbs2tm1Vcs/Bbs2tm1Vcs
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J))
|
absent sperm flagellum
|
J:94467
|
Bbs4Gt1Nk/Bbs4Gt1Nk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal olfactory epithelium cilium morphology
|
J:92950
|
Bbs4Gt1Nk/Bbs4Gt1Nk
(B6.129S7-Bbs4Gt1Nk)
|
enhanced autophagy
|
J:279506
|
Bbs4tm1Vcs/Bbs4tm1Vcs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
absent sperm flagellum
|
J:90812
|
Bbs4tm1Vcs/Bbs4tm1Vcs
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:137093
|
Bbs5tm1a(EUCOMM)Wtsi/Bbs5tm1a(EUCOMM)Wtsi
(C57BL/6-Bbs5tm1a(EUCOMM)Wtsi)
|
absent sperm flagellum
|
J:307098
|
Bbs7tm1Vcs/Bbs7tm1Vcs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal brain ependyma motile cilium morphology
|
J:226740
|
abnormal cilium morphology
|
J:226740
|
abnormal outer dense fiber morphology
|
J:226740
|
abnormal sperm axoneme morphology
|
J:226740
|
abnormal sperm flagellum morphology
|
J:226740
|
abnormal sperm principal piece morphology
|
J:226740
|
absent sperm flagellum
|
J:226740
|
cellular phenotype
|
J:226740
|
decreased brain ependyma motile cilium length
|
J:226740
|
decreased brain ependyma motile cilium number
|
J:226740
|
Bbs10tm1.2Vmar/Bbs10tm1.2Vmar
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal retina apoptosis
|
J:227230
|
Bbs12tm1.1Vmar/Bbs12tm1.1Vmar
(involves: 129S6/SvEvTac * C57BL/6)
|
increased adipocyte glucose uptake
|
J:189019
|
BC004004em1Nju/BC004004em1Nju
(C57BL/6J-BC004004em1Nju)
|
abnormal autophagosome formation
|
J:328326
|
abnormal fibroblast physiology
|
J:328326
|
abnormal lysosome morphology
|
J:328326
|
decreased lung fibroblast proliferation
|
J:328326
|
enhanced autophagy
|
J:328326
|
increased fibroblast apoptosis
|
J:328326
|
Bcap31tm1.1Bwang/Bcap31tm1.1Bwang Tg(Lck-cre)548Jxm/0
(involves: C57BL/6 * CBA)
|
decreased T cell proliferation
|
J:274469
|
increased thymocyte apoptosis
|
J:274469
|
Bcar1tm1Hhi/Bcar1tm1Hhi
(involves: 129S/SvEv * C57BL/6)
|
abnormal cell morphology
|
J:48967
|
abnormal cell physiology
|
J:48967
|
Bcas2tm1.1Lil/Bcas2tm1.1Lil Tg(Ddx4-cre)1Ptch/0
(Not Specified)
|
abnormal female meiosis
|
J:324155
|
abnormal oocyte morphology
|
J:324155
|
abnormal oogenesis
|
J:324155
|
Bcas2tm1.1Lil/Bcas2tm1.1Lil Tg(Zp3-cre)3Mrt/0
(involves: 129 * C57BL/6 * FVB/N * SJL)
|
maternal effect
|
J:239876
|
Bcas3tm1.1Msin/Bcas3tm1.1Msin
(involves: BALB/cJ * C57BL/6NCrlj * CBA/JNCrlj)
|
decreased cell migration
|
J:262744
|
Bckdhatm1a(EUCOMM)Hmgu/Bckdhatm1a(EUCOMM)Hmgu Tg(Ucp1-cre)1Evdr/0
(involves: C57BL/6N * FVB)
|
decreased fatty acid oxidation
|
J:278806
|
Bcl2tm1.1Sjk/Bcl2tm1.1Sjk Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129X1/SvJ * C57BL/6 * C57BL/6NCrj * SJL)
|
decreased skeletal muscle cell glucose uptake
|
J:181308
|
impaired autophagy
|
J:181308
|
Bcl2tm1Dlo/Bcl2tm1Dlo
(involves: 129P2/OlaHsd * C57BL/6)
|
increased kidney apoptosis
|
J:111022,
J:33776
|
increased renal glomerulus apoptosis
|
J:111022
|
Bcl2tm1Dlo/Bcl2tm1Dlo
(B6.129P2-Bcl2tm1Dlo)
|
increased B cell apoptosis
|
J:73316
|
increased splenocyte apoptosis
|
J:153846
|
increased T cell apoptosis
|
J:73316
|
Bcl2tm1Dlo/Bcl2tm1Dlo Bcl2l11tm1.1Ast/Bcl2l11+
(B6.129-Bcl2tm1Dlo Bcl2l11tm1.1Ast)
|
increased T cell apoptosis
|
J:73316
|
Bcl2tm1Dlo/Bcl2tm1Dlo Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast
(B6.129-Bcl2tm1Dlo Bcl2l11tm1.1Ast)
|
decreased B cell apoptosis
|
J:73316
|
increased T cell apoptosis
|
J:73316
|
Bcl2tm1Dlo/Bcl2tm1Dlo Bcl2l11tm3.1Boui/Bcl2l11tm3.1Boui
(B6.Cg-Bcl2tm1Dlo Bcl2l11tm3.1Boui)
|
decreased splenocyte apoptosis
|
J:153846
|
Bcl2tm1Irt/Bcl2tm1Irt Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased macrophage apoptosis
|
J:144243
|
Bcl2tm1Lbox/Bcl2tm1Lbox
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
decreased B cell proliferation
|
J:114637
|
increased B cell apoptosis
|
J:114637
|
Bcl2tm1Sjk/Bcl2tm1Sjk
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell adhesion
|
J:53123
|
absent oocytes
|
J:28173
|
increased kidney apoptosis
|
J:34504
|
increased kidney cell proliferation
|
J:15224,
J:34504
|
increased metanephric mesenchyme apoptosis
|
J:22552
|
increased T cell apoptosis
|
J:15224
|
Bcl2l1tm1Cant/Bcl2l1tm1Cant
(involves: 129S6/SvEvTac)
|
decreased T cell proliferation
|
J:77507
|
Bcl2l1tm1Dlo/Bcl2l1tm1Dlo
(Not Specified)
|
increased apoptosis
|
J:39573
|
increased neuron apoptosis
|
J:39573
|
Bcl2l1tm1Dlo/Bcl2l1tm1Dlo Casp9tm1Flv/?
(involves: 129S1/Sv * C57BL/6)
|
increased apoptosis
|
J:66953
|
increased neuron apoptosis
|
J:66953
|
Bcl2l1tm1Dlo/Bcl2l1tm1Dlo Casp9tm1Flv/Casp9tm1Flv
(involves: 129S1/Sv * C57BL/6)
|
decreased apoptosis
|
J:66953
|
increased apoptosis
|
J:66953
|
Bcl2l1tm1Mam/Bcl2l1tm1Mam
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal apoptosis
|
J:63161
|
decreased primordial germ cell number
|
J:63161
|
Bcl2l1tm1Tak/Bcl2l1tm1Tak Tg(KRT5-cre)1Tak/0
(involves: C3H * C57BL/6)
|
decreased keratinocyte adhesion
|
J:82661
|
increased cellular sensitivity to ultraviolet irradiation
|
J:82661
|
increased keratinocyte apoptosis
|
J:82661
|
Bcl2l2Gt(ROSA)41Sor/Bcl2l2Gt(ROSA)41Sor
(involves: 129S5/SvEvBrd)
|
abnormal Purkinje cell mitochondrial morphology
|
J:137190
|
decreased male germ cell number
|
J:46386
|
Bcl2l2Gt(ROSA)41Sor/Bcl2l2Gt(ROSA)41Sor
(involves: 129S5/SvEvBrd * C57BL/6J)
|
decreased germ cell number
|
J:70212
|
Bcl2l2Gt(ROSA)41Sor/Bcl2l2Gt(ROSA)41Sor Grid2ho-4J/Grid2ho-4J
(involves: 129S5/SvEvBrd * DBA/2J)
|
abnormal Purkinje cell mitochondrial morphology
|
J:137190
|
Bcl2l2tm1Sco/Bcl2l2tm1Sco
(involves: 129S1/Sv * C57BL/6 * FVB/N)
|
azoospermia
|
J:50338
|
increased male germ cell apoptosis
|
J:50338
|
multinucleated giant male germ cells
|
J:50338
|
Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast
(involves: 129S1/Sv * C57BL/6)
|
abnormal B cell proliferation
|
J:90963
|
decreased B cell apoptosis
|
J:90963
|
increased renal glomerulus apoptosis
|
J:132217
|
Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast
(B6.129S1-Bcl2l11tm1.1Ast)
|
decreased apoptosis
|
J:123409
|
decreased B cell apoptosis
|
J:73316
|
decreased T cell apoptosis
|
J:73316,
J:133084
|
Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast
(involves: 129S1/Sv)
|
decreased splenocyte apoptosis
|
J:266833
|
decreased thymocyte apoptosis
|
J:266833
|
Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast
(B6.129S1-Bcl2l11tm1.1Ast/J)
|
decreased T cell apoptosis
|
J:153652
|
Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast Biktm1Ast/Biktm1Ast
(B6.Cg-Bcl2l11tm1.1Ast Biktm1Ast)
|
arrest of male meiosis
|
J:103605
|
azoospermia
|
J:103605
|
multinucleated giant male germ cells
|
J:103605
|
Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast Bmftm1Rjd/Bmftm1Rjd
(B6.129S-Bcl2l11tm1.1Ast Bmftm1Rjd)
|
decreased T cell apoptosis
|
J:153652
|
Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast Faslpr/Faslpr
(B6.Cg-Bcl2l11tm1.1Ast Faslpr)
|
increased kidney cell proliferation
|
J:132217
|
increased renal glomerulus apoptosis
|
J:132217
|
Bcl2l11tm1.1Ast/Bcl2l11tm1.1Ast Mlf1tm1Swm/Mlf1tm1Swm
(involves: 129S1/Sv * C57BL/6)
|
decreased splenocyte apoptosis
|
J:266833
|
decreased thymocyte apoptosis
|
J:266833
|
Bcl2l11tm2Rjd/Bcl2l11tm2Rjd
(B6.129S6-Bcl2l11tm2Rjd)
|
increased fibroblast apoptosis
|
J:137061
|
Bcl2l11tm3Rjd/Bcl2l11tm3Rjd
(B6.129S6-Bcl2l11tm3Rjd)
|
decreased thymocyte apoptosis
|
J:137061
|
Bcl2l11tm4Rjd/Bcl2l11tm4Rjd
(B6.129S6-Bcl2l11tm4Rjd)
|
increased fibroblast apoptosis
|
J:137061
|
Bcl3tm1Sbn/Bcl3tm1Sbn
(involves: 129S4/SvJae)
|
decreased B cell proliferation
|
J:207111
|
increased B cell proliferation
|
J:207111
|
Bcl6tm1.1Toka/Bcl6+ Tg(TcraTcrb)425Cbn/0
(involves: BALB/c * C57BL/6 * NZB)
|
decreased T cell proliferation
|
J:174014
|
Bcl6tm1.1Toka/Bcl6tm1.1Toka Tg(IghelMD4)4Ccg/0
(involves: C57BL/6 * NZB)
|
increased activation-induced B cell apoptosis
|
J:174014
|
Bcl6tm1Gdba/Bcl6tm1Gdba Tg(Adipoq-cre)1Evdr/0
(involves: C57BL/6 * FVB/NJ)
|
decreased adipocyte glucose uptake
|
J:271078
|
increased adipocyte glucose uptake
|
J:271078
|
increased skeletal muscle cell glucose uptake
|
J:271078
|
Bcl6tm1Htno/Bcl6+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal apoptosis
|
J:82037
|
Bcl6tm1Htno/Bcl6tm1Htno
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
cardiac interstitial fibrosis
|
J:55952
|
Bcl6tm1Htno/Bcl6tm1Htno
(involves: 129S1/Sv * 129X1/SvJ)
|
increased male germ cell apoptosis
|
J:82037
|
oligozoospermia
|
J:82037
|
Bcl6tm2Rdf/Bcl6tm2Rdf
(involves: 129S1/Sv)
|
decreased B cell proliferation
|
J:40769
|
Bcl6btm1Dtf/Bcl6btm1Dtf
(involves: 129P2/OlaHsd)
|
decreased T cell proliferation
|
J:99818
|
Bcl10tm1Mak/Bcl10tm1Mak
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:67297
|
decreased B cell proliferation
|
J:109545,
J:67297
|
decreased T cell proliferation
|
J:109545,
J:67297
|
increased hindbrain apoptosis
|
J:67297
|
Bcl10tm1Swm/Bcl10tm1Swm
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:85147
|
Bcl11atm1Ngc/Bcl11atm1Ngc
(involves: 129S1/Sv * C57BL/6J)
|
abnormal dendritic cell differentiation
|
J:207383
|
Bcl11atm1Pwt/Bcl11atm1Pwt Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ Tg(Mx1-cre)1Cgn/0
(involves: 129X1/SvJ * C57BL/6 * CBA)
|
abnormal dendritic cell differentiation
|
J:207383
|
Bcl11atm1Sbri/Bcl11atm1Sbri Tg(Pou3f4-cre)32Cren/0
(involves: CD-1)
|
abnormal neuron differentiation
|
J:184011
|
Bcl11atm2.1Peli/Bcl11atm2.1Peli Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S1/Sv)
|
increased B cell apoptosis
|
J:194616
|
Bcl11btm1Jpk/Bcl11btm1Jpk
(involves: BALB/c * C57BL/6 * CBA)
|
increased thymocyte apoptosis
|
J:83651
|
Bcl11btm2.1Jpk/Bcl11b+ Tg(Lck-cre)1Jtak/0
(involves: C57BL/6)
|
abnormal cell cycle
|
J:210122
|
Bclaf1tm1Raz/Bclaf1+
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:158087
|
Bclaf1tm1Raz/Bclaf1tm1Raz
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal mesenchymal cell differentiation involved in lung development
|
J:158087
|
decreased T cell proliferation
|
J:158087
|
Bco2tm1Dnp/Bco2tm1Dnp
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal aerobic respiration
|
J:170742
|
Bcortm1.1Vjba/Y
(involves: 129S1/Sv)
|
increased cell proliferation
|
J:231455
|
Bcorl1em1Nju/Y
(C57BL/6J-Bcorl1em1Nju)
|
abnormal sperm mitochondrial sheath morphology
|
J:310942
|
oligozoospermia
|
J:310942
|
Bcs1ltm1.1Levp/Bcs1ltm1.1Levp
(involves: 129 * 129S6/SvEvTac * C57BL/6)
|
abnormal cellular respiration
|
J:189652
|
abnormal mitochondrial physiology
|
J:189652
|
increased mitochondrial size
|
J:189652
|
Bcs1ltm1.1Levp/Bcs1ltm1.1Levp
(B6.129-Bcs1ltm1.1Levp)
|
abnormal hepatocyte mitochondrial morphology
|
J:273501
|
abnormal mitochondrial crista morphology
|
J:273501
|
abnormal mitochondrial physiology
|
J:273501
|
Bdkrb2tm1Jfh/Bdkrb2tm1Jfh
(B6.129S7-Bdkrb2tm1Jfh)
|
abnormal mitochondrial chromosome morphology
|
J:108948
|
Bdkrb2tm1Jfh/Bdkrb2tm1Jfh Ins2Akita/Ins2+
(B6.Cg-Ins2Akita Bdkrb2tm1Jfh)
|
abnormal mitochondrial chromosome morphology
|
J:108948
|
abnormal spermatogonia morphology
|
J:108948
|
Bdnftm1Jae/Bdnftm1Jae
(involves: 129S4/SvJae)
|
increased neuron apoptosis
|
J:123022
|
Bdnftm1Jae/Bdnftm1Jae
(involves: 129S4/SvJae * BALB/c)
|
abnormal neuron apoptosis
|
J:46125
|
Bdnftm1Lfr/Bdnftm1Lfr
(involves: 129S2/SvPas * C57BL/6)
|
abnormal neuron differentiation
|
J:67231
|
Bdnftm1Meg/Bdnftm1Meg
(Not Specified)
|
abnormal axon pruning
|
J:139381
|
Bdnftm1Par/Bdnftm1Par
(involves: 129S1/Sv)
|
increased neuron apoptosis
|
J:60927
|
Bdnftm1Par/Bdnftm1Par Ntf5tm1Par/Ntf5tm1Par
(involves: 129S1/Sv * C57BL/6)
|
abnormal neuron differentiation
|
J:60927
|
Bdnftm1Tbn/Bdnftm1Tbn
(involves: 129S4/SvJae * NMRI)
|
abnormal colon goblet cell morphology
|
J:110612
|
Becn1tm1.1Bflu/Becn1tm1.1Bflu Tg(Cd4-cre)1Cwi/0
(involves: 129S1/Sv * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:203090
|
increased T cell apoptosis
|
J:203090
|
Becn1tm1Blev/Becn1+
(involves: 129X1/SvJ * C57BL/6J)
|
impaired autophagy
|
J:86953
|
Becn1tm1Blev/Becn1+ Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrj)
|
impaired autophagy
|
J:86953
|
Becn1tm1Blev/Becn1+ Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129X1/SvJ * C57BL/6NCrj)
|
impaired autophagy
|
J:181308
|
Becn1tm1Htz/Becn1tm1Htz
(involves: 129P2/OlaHsd)
|
impaired autophagy
|
J:86982
|
increased embryonic tissue cell apoptosis
|
J:86982
|
Becn1tm2.1Blev/Becn1tm2.1Blev Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129 * C57BL/6 * C57BL/6J * C57BL/6NCrlj * DBA/2)
|
enhanced autophagy
|
J:244104
|
Becn2tm1.1Blev/Becn2+
(B6.Cg-Becn2tm1.1Blev)
|
impaired autophagy
|
J:203842
|
Becn2tm1.1Blev/Becn2tm1.1Blev
(B6.Cg-Becn2tm1.1Blev)
|
impaired autophagy
|
J:203842
|
bella/bella
(involves: BALB/c * C3H/HeH)
|
increased neuron apoptosis
|
J:230923,
J:177995
|
Bend2em1Hncs/0
(B6.Cg-Bend2em1Hncs)
|
arrest of male meiosis
|
J:325496
|
azoospermia
|
J:325496
|
increased male germ cell apoptosis
|
J:325496
|
Best1tm1Web/Best1tm1Web
(B6.129S1-Best1tm1Web)
|
abnormal acrosome morphology
|
J:221655
|
abnormal sperm flagellum morphology
|
J:221655
|
Best1tm1Web/Best1tm1Web
(involves: CD-1)
|
abnormal acrosome morphology
|
J:221655
|
absent acrosome
|
J:221655
|
asthenozoospermia
|
J:221655
|
coiled sperm flagellum
|
J:221655
|
detached sperm flagellum
|
J:221655
|
kinked sperm flagellum
|
J:221655
|
necrospermia
|
J:221655
|
Best1tm2.1Web/Best1tm2.1Web
(involves: 129S1/Sv * CD-1)
|
asthenozoospermia
|
J:280642
|
Best3tm1.1Zhoj/Best3tm1.1Zhoj Tg(Tagln-cre)1Her/0
(involves: C57BL/6 * SJL)
|
increased apoptosis
|
J:338981
|
Bfsp2Dundee/Bfsp2Dundee
(129X1/SvJ)
|
abnormal cell cytoskeleton morphology
|
J:85325
|
Bfsp2tm1Raq/Bfsp2tm1Raq
(involves: 129P2/OlaHsd)
|
abnormal cell cytoskeleton morphology
|
J:82327
|
Bglap/Bglap2tm3.1Kry/Bglap/Bglap2tm3.1Kry Tg(Col1a1-cre)1Kry/0
(involves: FVB)
|
oligozoospermia
|
J:170888
|
Bglap/Bglap2tm3.1Kry/Bglap+ Gprc6atm1.1Kry/Gprc6a+ Tg(Cyp17a1-icre)AJako/0
(involves: C57BL/6J)
|
oligozoospermia
|
J:170888
|
Bglap/Bglap2tm3.1Kry/Bglap2+ Gprc6atm1.1Kry/Gprc6a+ Tg(Cyp17a1-icre)AJako/0
(involves: C57BL/6J)
|
oligozoospermia
|
J:170888
|
Bglap/Bglap2tm3.1Kry/Bglap/Bglap2tm3.1Kry Tg(Col1a1-cre)1Kry/0
(involves: FVB)
|
oligozoospermia
|
J:170888
|
Bgntm1Mfy/Y Fmodtm1Aol/Fmodtm1Aol
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
decreased chondrocyte proliferation
|
J:117908
|
increased apoptosis
|
J:112779
|
Bgntm1Mfy/Bgntm1Mfy Fmodtm1Aol/Fmodtm1Aol
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
decreased chondrocyte proliferation
|
J:117908
|
Bhlha9tm1Nba/Bhlha9tm1Nba
(involves: 129S/SvEv * C57BL/6 * C57BL/6N)
|
abnormal interdigital cell death
|
J:214852
|
Bhlha15tm3(cre/ERT2)Skz/Bhlha15tm3(cre/ERT2)Skz
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal autophagy
|
J:239144
|
Bhlhe22tm1Meg/Bhlhe22tm1Meg
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal axon guidance
|
J:182304
|
Bhlhe23tm1Dbra/Bhlhe23tm1Dbra
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased retina apoptosis
|
J:92623
|
Bhlhe40tm1Tan/Bhlhe40tm1Tan
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
decreased T cell proliferation
|
J:72651
|
Bhlhe41tm1.2Cdon/Bhlhe41tm1.2Cdon
(B6.129S6-Bhlhe41tm1.2Cdon)
|
decreased T cell proliferation
|
J:157740
|
Bicc1tm1Bdc/Bicc1tm1Bdc
(involves: 129 * C57BL/6)
|
abnormal embryonic cilium location or orientation
|
J:152173
|
abnormal motile primary cilium physiology
|
J:152173
|
Bicd2tm1.1Hgrd/Bicd2tm1.1Hgrd
(involves: C57BL/6)
|
abnormal cerebellar granule cell migration
|
J:210236
|
abnormal extracellular matrix morphology
|
J:210236
|
Bicd2tm1Hgrd/Bicd2tm1Hgrd Emx1tm1(cre)Krj/Emx1+
(involves: C57BL/6)
|
abnormal neuronal migration
|
J:210236
|
Bicd2tm1Hgrd/Bicd2tm1Hgrd Tg(GFAP-cre)25Mes/0
(involves: C57BL/6 * FVB/N)
|
abnormal cerebellar granule cell migration
|
J:210236
|
abnormal neuronal migration
|
J:210236
|
Bidtm1.1Ast/Bidtm1.1Ast
(involves: BALB/cJ * C57BL/6 * NZB)
|
cellular phenotype
|
J:158191
|
Bidtm1Sjk/Bidtm1Sjk
(involves: 129X1/SvJ)
|
abnormal mitochondrial physiology
|
J:57073
|
decreased apoptosis
|
J:57073
|
Bidtm1Sjk/Bidtm1Sjk Relatm1Bal/Relatm1Bal
(involves: 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
decreased fibroblast apoptosis
|
J:117693
|
Bin1tm1Gcp/Bin1tm1Gcp
(involves: 129S6/SvEvTac * C57BL/6J)
|
cellular phenotype
|
J:83753
|
Bin1tm1Gcp/Bin1tm2Gcp Tg(MMTV-Myc)141-3Led/0 Tg(Wap-cre)11738Mam/0
(involves: 129S6/SvEvTac * C57BL/6 * CD-1 * FVB/N * SJL)
|
abnormal cell physiology
|
J:117330
|
decreased apoptosis
|
J:117330
|
increased cell proliferation
|
J:117330
|
Birc2tm1Rbr/Birc2tm1Rbr Birc3tm1.1Rbr/Birc3tm1.1Rbr Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C57BL/6 * NZB)
|
decreased B cell apoptosis
|
J:172843
|
Birc2tm2.1Jda/Birc2tm2.1Jda
(B6.Cg-Birc2tm2.1Jda)
|
increased T cell proliferation
|
J:199221
|
Birc3tm1Jda/Birc3tm1Jda
(B6.Cg-Birc3tm1Jda)
|
decreased B cell apoptosis
|
J:166899
|
increased B cell proliferation
|
J:166899
|
Birc3tm1Jda/Birc3tm1Jda
(involves: 129 * C57BL/6)
|
increased T cell proliferation
|
J:199221
|
Birc5tm1Emc/Birc5+
(involves: 129S1/Sv * 129X1/SvJ * Swiss)
|
abnormal apoptosis
|
J:78103
|
abnormal oxidative phosphorylation
|
J:78103
|
Birc5tm1Mak/Birc5tm1Mak Tg(Lck-cre)I57Jxm/0
(involves: 129P2/OlaHsd)
|
abnormal cell cycle
|
J:90892
|
increased T cell apoptosis
|
J:90892
|
Birc5tm1Vaux/Birc5tm1Vaux
(C57BL/6-Birc5tm1Vaux)
|
abnormal cell cycle
|
J:86384
|
abnormal cell nucleus count
|
J:86384
|
abnormal cell nucleus morphology
|
J:86384
|
abnormal mitotic spindle morphology
|
J:86384
|
binucleate
|
J:86384
|
Birc6tm1Nai/Birc6tm1Nai
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell cycle
|
J:96768
|
increased fibroblast apoptosis
|
J:96768
|
increased thymocyte apoptosis
|
J:96768
|
Birc6tm1Sjen/Birc6tm1Sjen
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:94169
|
Blmtm1Ches/Blmtm1Ches
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
abnormal apoptosis
|
J:50843
|
abnormal cell morphology
|
J:50843
|
Blmtm1Grdn/Blm+
(involves: 129P2/OlaHsd * Black Swiss)
|
chromosome breakage
|
J:79058
|
Blmtm4Ches/Blmtm4Ches Cd19tm1(cre)Cgn/Cd19+ Nsmce2tm2.1Ofc/Nsmce2tm2.1Ofc
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * SJL)
|
elevated level of mitotic sister chromatid exchange
|
J:227197
|
Blnktm1Achn/Blnk+
(involves: 129S4/SvJae * 129X1/SvJ * BALB/c * C3H * C57BL/6)
|
decreased B cell proliferation
|
J:82430
|
Blnktm1Achn/Blnk+ Btktm1Wk/Btktm1Wk Tg(IGH-Btk)1Witt/0
(involves: 129S4/SvJae * 129X1/SvJ * BALB/c * C3H * C57BL/6)
|
decreased B cell proliferation
|
J:82430
|
Blnktm1Dkit/Blnktm1Dkit
(involves: C57BL/6)
|
abnormal B cell apoptosis
|
J:143854
|
increased B cell apoptosis
|
J:143854
|
Blnktm1Dkit/Blnktm1Dkit Prkcdtm1Kin/Prkcdtm1Kin
(involves: 129P2/OlaHsd * C57BL/6 * NZB)
|
abnormal B cell proliferation
|
J:143854
|
increased B cell apoptosis
|
J:143854
|
Blnktm1Kplm/Blnktm1Kplm
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:61130
|
increased B cell apoptosis
|
J:131161
|
Blnktm1Kplm/Blnktm1Kplm Plcg2tm1.1Kuro/Plcg2+
(involves: 129P2/OlaHsd)
|
increased B cell apoptosis
|
J:131161
|
Blnktm1Kplm/Blnktm1Kplm Plcg2tm1.1Kuro/Plcg2tm1.1Kuro
(involves: 129P2/OlaHsd)
|
increased B cell apoptosis
|
J:131161
|
Bloc1s1tm1.1Wli/Bloc1s1tm1.1Wli
(involves: 129 * C57BL/6J)
|
abnormal autophagy
|
J:238911
|
abnormal lysosome morphology
|
J:238911
|
abnormal vesicle-mediated transport
|
J:238911
|
cellular phenotype
|
J:238623
|
Bloc1s1tm1a(EUCOMM)Hmgu/Bloc1s1tm1a(EUCOMM)Hmgu
(C57BL/6N-Atm1Brd Bloc1s1tm1a(EUCOMM)Hmgu/Ics)
|
abnormal autophagy
|
J:213033
|
abnormal mitochondrial physiology
|
J:213033
|
abnormal mitophagy
|
J:213033
|
Bloc1s2tm1Wli/Bloc1s2tm1Wli
(involves: 129 * C57BL/6J)
|
abnormal lysosome morphology
|
J:238623
|
abnormal lysosome physiology
|
J:238623
|
abnormal vesicle-mediated transport
|
J:238623
|
impaired neuron differentiation
|
J:238623
|
increased hematopoietic stem cell proliferation
|
J:238623
|
increased neuronal precursor proliferation
|
J:238623
|
increased radial glial cell number
|
J:238623
|
Bloc1s3rp/Bloc1s3rp
(involves: C57BL/10ScSn * C57BL/Tb)
|
abnormal lysosome physiology
|
J:6801,
J:6470
|
Bloc1s4cno/Bloc1s4cno
(C3H/HeJ-Bloc1s4cno)
|
abnormal vesicle-mediated transport
|
J:83960
|
decreased lysosomal enzyme secretion
|
J:61187
|
decreased platelet ATP level
|
J:61187
|
Bloc1s5mu/Bloc1s5mu
(involves: STOCK t)
|
decreased platelet ATP level
|
J:29151
|
lysosomal protein accumulation
|
J:29151
|
Bloc1s5mu/Bloc1s5mu
(CHMU/Le)
|
decreased lysosomal enzyme secretion
|
J:29151
|
Bloc1s6pa/Bloc1s6pa
(B6.Cg-Bloc1s6pa/J)
|
abnormal lysosome physiology
|
J:6801
|
decreased platelet ATP level
|
J:7327
|
Bloc1s6pa/Bloc1s6pa
(Not Specified)
|
cellular phenotype
|
J:238623
|
maternal effect
|
J:5680
|
Blvratm1.1Rsto/Blvratm1.1Rsto
(involves: C57BL/6)
|
oxidative stress
|
J:331733
|
Blvratm1c(EUCOMM)Hmgu/Blvratm1c(EUCOMM)Hmgu Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6J * C57BL/6N)
|
decreased fatty acid beta-oxidation
|
J:237631
|
Bmal1tm1Bra/Bmal1tm1Bra
(B6.129-Bmal1tm1Bra)
|
impaired leukocyte tethering or rolling
|
J:191844
|
Bmftm1.1Ast/Bmftm1.1Ast
(B6.Cg-Bmftm1.1Anst)
|
decreased B cell apoptosis
|
J:133084
|
decreased T cell apoptosis
|
J:133084
|
Bmftm1Rjd/Bmftm1Rjd
(B6.129S6-Bmftm1Rjd)
|
decreased T cell apoptosis
|
J:153652
|
Bmi1tm1.1Lees/Bmi1tm1.1Lees Apctm2Cip/Apc+ Tg(Vil1-cre)20Syr/0
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2)
|
cellular phenotype
|
J:204354
|
Bmi1tm1Brn/Bmi1tm1Brn
(either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * FVB))
|
decreased splenocyte proliferation
|
J:17712
|
Bmi1tm1Brn/Bmi1tm1Brn
(involves: 129P2/OlaHsd)
|
abnormal cell cycle
|
J:134271
|
abnormal male germ cell physiology
|
J:286451
|
abnormal sperm head morphology
|
J:286451
|
abnormal sperm mitochondrial sheath morphology
|
J:286451
|
abnormal sperm nucleus morphology
|
J:286451
|
decreased cell proliferation
|
J:134271
|
decreased male germ cell number
|
J:286451
|
detached acrosome
|
J:286451
|
early cellular replicative senescence
|
J:134271,
J:198334
|
enlarged sperm head
|
J:286451
|
increased male germ cell apoptosis
|
J:286451
|
oligozoospermia
|
J:286451
|
oxidative stress
|
J:286451
|
teratozoospermia
|
J:286451
|
Bmi1tm1Brn/Bmi1tm1Brn
(involves: 129P2/OlaHsd * C57BL/6J * FVB/N)
|
abnormal mitochondrial crista morphology
|
J:287217
|
abnormal mitochondrial morphology
|
J:287217
|
decreased granulosa cell proliferation
|
J:287217
|
decreased mitochondrial number
|
J:287217
|
decreased oocyte number
|
J:287217
|
increased granulosa cell apoptosis
|
J:287217
|
oxidative stress
|
J:287217
|
Bmi1tm1Brn/Bmi1tm1Brn Apctm2Cip/Apc+ Tg(Vil1-cre)20Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
increased apoptosis
|
J:204354
|
Bmi1tm1Brn/Bmi1tm1Brn E2f6tm1Lees/E2f6tm1Lees
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:134271
|
decreased cell proliferation
|
J:134271
|
early cellular replicative senescence
|
J:134271
|
Bmp2tm1.1Mis/Bmp2tm1.2Mis Tg(Col1a1-cre)1Bek/0
(involves: 129S4/SvJaeSor * 129S7/SvEvBrd * CD-1)
|
impaired osteoblast differentiation
|
J:210409
|
Bmp2tm1Cjt/Bmp2tm1Cjt Bmp4tm1Jfm/Bmp4tm1Jfm Tg(Prrx1-cre)1Cjt/0
(involves: 129S4/SvJaeSor * C57BL/6 * SJL)
|
abnormal interdigital cell death
|
J:118257
|
Bmp4tm1.1Jlch/Bmp4+
(B6.129-Bmp4tm1.1Jlch)
|
decreased primordial germ cell number
|
J:108516
|
Bmp4tm1.1Jlch/Bmp4tm1.1Jlch
(B6.129-Bmp4tm1.1Jlch)
|
decreased primordial germ cell number
|
J:108516
|
Bmp4tm1Blh/Bmp4+
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
decreased primordial germ cell number
|
J:53311,
J:199855
|
Bmp4tm1Blh/Bmp4+
(involves: 129S2/SvPas * 129S6/SvEvTac)
|
decreased primordial germ cell number
|
J:53311
|
Bmp4tm1Blh/Bmp4+ Bmp8btm1Blh/Bmp8b+
(involves: 129/Sv * 129S2/SvPas * Black Swiss)
|
decreased primordial germ cell number
|
J:63160
|
Bmp4tm1Blh/Bmp4+ Ctdnep1tm1Ryn/Ctdnep1tm1Ryn
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * CBA)
|
decreased primordial germ cell number
|
J:199855
|
Bmp4tm1Blh/Bmp4+ Tg(Prdm14-Venus)1Sait/0
(involves: 129S2/SvPas)
|
decreased primordial germ cell number
|
J:138571
|
Bmp4tm1Blh/Bmp4tm1Blh
(involves: 129S2/SvPas * Black Swiss)
|
absent primordial germ cells
|
J:53311
|
Bmp4tm1Blh/Bmp4tm1Blh
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
absent primordial germ cells
|
J:53311
|
Bmp4tm1Jfm/Bmp4tm1Jfm H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S4/SvJaeSor * C57BL/6J * CBA/J)
|
impaired osteoblast differentiation
|
J:181229
|
Bmp4tm2Blh/Bmp4+
(involves: 129S6/SvEvTac * Black Swiss)
|
decreased primordial germ cell number
|
J:53311
|
Bmp4tm2Blh/Bmp4+
(involves: 129S6/SvEvTac * Black Swiss * C57BL/6J)
|
increased metanephric mesenchyme apoptosis
|
J:82895
|
Bmp4tm2Blh/Bmp4tm2Blh
(involves: 129S6/SvEvTac * Black Swiss)
|
absent primordial germ cells
|
J:53311
|
Bmp7tm1Rob/Bmp7+ Bmp8atm1Blh/Bmp8atm1Blh
(involves: 129S/SvEv * 129S6/SvEvTac * Black Swiss * C57BL/6)
|
abnormal male germ cell morphology
|
J:78867
|
Bmp8atm1Blh/Bmp8a+
(involves: 129S6/SvEvTac * Black Swiss)
|
abnormal male germ cell morphology
|
J:46927
|
Bmp8atm1Blh/Bmp8a+ Bmp8btm1Blh/Bmp8b+
(involves: 129/Sv * 129S6/SvEvTac * Black Swiss)
|
abnormal male germ cell morphology
|
J:46927
|
Bmp8atm1Blh/Bmp8atm1Blh
(involves: 129S6/SvEvTac * Black Swiss)
|
increased male germ cell apoptosis
|
J:46927
|
Bmp8btm1Blh/Bmp8b+
(either: B6.129-Bmp8btm1Blh or (involves: 129 * Black Swiss * C57BL/6))
|
decreased primordial germ cell number
|
J:63160
|
Bmp8btm1Blh/Bmp8btm1Blh
(involves: 129/Sv * Black Swiss)
|
abnormal cell differentiation
|
J:34057
|
abnormal male germ cell morphology
|
J:34057
|
abnormal primordial germ cell morphology
|
J:63160
|
abnormal spermatogonia proliferation
|
J:34057
|
absent primordial germ cells
|
J:63160
|
decreased male germ cell number
|
J:34057
|
decreased primordial germ cell number
|
J:63160
|
increased male germ cell apoptosis
|
J:34057
|
Bmp8btm1Blh/Bmp8btm1Blh
(either: B6.129-Bmp8btm1Blh or (involves: 129 * Black Swiss * C57BL/6))
|
absent primordial germ cells
|
J:63160
|
Bmp8btm1Blh/Bmp8btm1Blh
(B6.129-Bmp8btm1Blh)
|
absent primordial germ cells
|
J:63160
|
Bmp10tm1.1(Gdf2)Minh/Bmp10tm1.1(Gdf2)Minh
(C57BL/6N-Bmp10tm1.1(Gdf2)Minh)
|
decreased fetal cardiomyocyte proliferation
|
J:222016
|
Bmp15tm1Zuk/Bmp15tm1Zuk
(involves: 129S7/SvEvBrd)
|
abnormal zona pellucida morphology
|
J:69611
|
Bmp15tm1Zuk/Bmp15tm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal oocyte morphology
|
J:69611
|
abnormal zona pellucida morphology
|
J:69611
|
decreased oocyte number
|
J:69611
|
Bmp15tm1Zuk/Bmp15tm1Zuk Gdf9tm1Zuk/Gdf9+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal oocyte morphology
|
J:69611
|
abnormal zona pellucida morphology
|
J:69611
|
decreased oocyte number
|
J:69611
|
Bmp15tm1Zuk/Bmp15tm1Zuk Gdf9tm1Zuk/Gdf9+
(involves: 129S7/SvEvBrd)
|
abnormal oocyte morphology
|
J:69611
|
abnormal zona pellucida morphology
|
J:69611
|
decreased oocyte number
|
J:69611
|
Bmp15tm1Zuk/Bmp15tm1Zuk Gdf9tm1Zuk/Gdf9tm1Zuk
(either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J))
|
abnormal zona pellucida morphology
|
J:69611
|
absent oocytes
|
J:69611
|
Bmpr1atm1Bhr/Bmpr1atm1Bhr
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased embryonic epiblast cell proliferation
|
J:30426
|
increased embryonic epiblast cell apoptosis
|
J:30426
|
Bmpr1atm1Bhr/Bmpr1atm1Bhr
(B6.129S7-Bmpr1atm1Bhr)
|
decreased embryonic epiblast cell proliferation
|
J:30426
|
increased embryonic epiblast cell apoptosis
|
J:30426
|
Bmpr1atm1Bhr/Bmpr1atm1Bhr
(involves: 129S7/SvEvBrd * Swiss)
|
decreased embryonic epiblast cell proliferation
|
J:30426
|
increased embryonic epiblast cell apoptosis
|
J:30426
|
Bmpr1atm1Bhr/Bmpr1atm1Bhr
(129S7/SvEvBrd-Bmpr1atm1Bhr)
|
decreased embryonic epiblast cell proliferation
|
J:30426
|
increased embryonic epiblast cell apoptosis
|
J:30426
|
Bmpr1atm1Bhr/Bmpr1atm2.1Bhr Bmpr1btm1Kml/Bmpr1btm1Kml Tg(Six3-cre)69Frty/0
(involves: 129S/SvEv)
|
increased retina apoptosis
|
J:96964
|
Bmpr1atm2.1Bhr/Bmpr1atm2.1Bhr Tg(Col1a1-cre/Esr1*)1Mis/0
(involves: 129S7/SvEvBrd)
|
abnormal osteoclast differentiation
|
J:143588
|
Bmpr1atm2.1Bhr/Bmpr1atm2.2Bhr Isl1tm1(cre)Sev/Isl1+
(involves: 129S4/SvJae * 129S7/SvEvBrd)
|
abnormal cardiomyocyte apoptosis
|
J:107396
|
abnormal fetal cardiomyocyte proliferation
|
J:107396
|
decreased cell proliferation
|
J:107396
|
Bmpr1bTg(ACTB-FLP)4917Dym/Bmpr1bTg(ACTB-FLP)4917Dym
(involves: C57BL/6 * SJL)
|
decreased cell proliferation
|
J:59288
|
increased apoptosis
|
J:59288
|
Bmpr1btm1Kml/Bmpr1btm1Kml
(involves: 129S/SvEv)
|
abnormal axon guidance
|
J:82686
|
increased retina apoptosis
|
J:82686
|
Bmpr2tm1.1Enl/Bmpr2tm1.1Enl Tg(Acvrl1-cre)L1Spo/0
(involves: 129S4/SvJae * FVB)
|
increased lung endothelial cell proliferation
|
J:158116
|
increased vascular smooth muscle cell proliferation
|
J:158116
|
Bmyctm1Mpo/Bmyctm1Mpo
(involves: 129S7/SvEvBrd * C57BL/6N)
|
increased male germ cell apoptosis
|
J:191587
|
Bnip3tm1Gwd/Bnip3tm1Gwd
(Not Specified)
|
decreased cardiomyocyte apoptosis
|
J:127533
|
Bnip3ltm1.1Gwd/Bnip3ltm1.1Gwd Tg(Myh6-Gnaq)#Gwd/0
(involves: 129 * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:145086
|
Bnip3ltm1Gwd/Bnip3ltm1Gwd Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129 * 129S7/SvEvBrd)
|
decreased cardiomyocyte apoptosis
|
J:145086
|
Bnip3ltm1Ney/Bnip3ltm1Ney
(Not Specified)
|
abnormal mitophagy
|
J:141545
|
Bola3tm1a(EUCOMM)Wtsi/Bola3tm1a(EUCOMM)Wtsi Tg(Adipoq-cre)1Evdr/0
(involves: C57BL/6 * C57BL/6N * FVB/NJ)
|
abnormal mitochondrial physiology
|
J:287367
|
decreased adipocyte glucose uptake
|
J:287367
|
Bolltm1Eyx/Bolltm1Eyx
(involves: 129 * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:160482
|
azoospermia
|
J:160482
|
multinucleated giant male germ cells
|
J:160482
|
Borcs5em1Jusb/Borcs5em1Jusb
(C57BL/6-Borcs5em1Jusb)
|
abnormal lysosome morphology
|
J:299228
|
Borcs6tm1.1(KOMP)Vlcg/Borcs6tm1.1(KOMP)Vlcg
(B6N(Cg)-Borcs6tm1.1(KOMP)Vlcg/J)
|
abnormal cell nucleus morphology
|
J:329966
|
abnormal lysosome morphology
|
J:329966
|
abnormal vesicle-mediated transport
|
J:329966
|
decreased embryonic epiblast cell proliferation
|
J:329966
|
increased embryonic tissue cell apoptosis
|
J:329966
|
Borcs7Q87X/Borcs7Q87X
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2)
|
abnormal lysosome morphology
|
J:271219
|
Borcs7tm1Bhk/Borcs7tm1Bhk
(129S6/SvEvTac-Borcs7tm1Bhk)
|
abnormal lysosome morphology
|
J:271219
|
bpck/bpck
(B6C3Fe a/a-bpck/J)
|
abnormal kidney epithelial cell primary cilium morphology
|
J:144929
|
increased kidney epithelial cell primary cilium length
|
J:144929
|
Bpnt1tm1Yrk/Bpnt1tm1Yrk
(involves: 129S/SvEv * C57BL/6)
|
abnormal hepatocyte mitochondrial morphology
|
J:194247
|
BptfGt(XG023)Byg/BptfGt(XG023)Byg
(involves: 129P2/OlaHsd)
|
decreased cell proliferation
|
J:147414
|
Bptftm1.1Cwu/Bptftm1.1Cwu Emx1tm1(cre)Krj/Emx1+
(involves: 129S1/Sv * 129S2/SvPas * C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:334252
|
increased neuron apoptosis
|
J:334252
|
Braftm1(ARAF)Urr/Braftm1(ARAF)Urr
(involves: 129S1/Sv * C57BL/6)
|
increased apoptosis
|
J:112971
|
Braftm1.1Sva/Braftm1.1Sva
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased neuron apoptosis
|
J:121660
|
Braftm1.1Wds/Braftm1.1Wds
(involves: 129P2/OlaHsd * C57BL/6)
|
increased neuron apoptosis
|
J:121660
|
Braftm1Bbd/Braf+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell morphology
|
J:170095
|
increased splenocyte apoptosis
|
J:170095
|
increased thymocyte apoptosis
|
J:170095
|
Braftm1Bbd/Braf+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1)
|
abnormal cell morphology
|
J:170095
|
increased splenocyte apoptosis
|
J:170095
|
increased thymocyte apoptosis
|
J:170095
|
Braftm1Bbd/Braf+
(B6.129-Braftm1Bbd)
|
abnormal cell morphology
|
J:170095
|
increased splenocyte apoptosis
|
J:170095
|
increased thymocyte apoptosis
|
J:170095
|
Braftm1Cpri/Braf+
(involves: 129P2/OlaHsd)
|
increased cell proliferation
|
J:187371
|
Braftm1Cpri/Braftm1Cpri
(involves: 129P2/OlaHsd * C57BL/6)
|
increased fibroblast proliferation
|
J:104375
|
Braftm1Mmcm/Braf+ Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ Tg(Mitf-cre)7114Gsb/0
(STOCK Braftm1Mmcm Gt(ROSA)26Sortm14(CAG-tdTomato)Hze Tg(Mitf-cre)7114Gsb/Cvrk)
|
abnormal cell physiology
|
J:312561
|
Braftm1Sva/Braftm1.1Sva Raf1tm1Bacc/Raf1tm2Bacc Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal axon extension
|
J:121660
|
Braftm1Sva/Braftm1Sva Krastm1Bbd/Kras+ Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:172200
|
Braftm1Sva/Braftm1Sva Krastm1Bbd/Kras+ Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd Raf1tm2Bacc/Raf1tm2Bacc
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:172200
|
Braftm1Sva/Braftm1Sva Raf1tm2Bacc/Raf1tm2Bacc
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal axon extension
|
J:121660
|
Braftm1Wds/Braftm1.1Wds Raf1tm1Bacc/Raf1tm2Bacc Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal axon extension
|
J:121660
|
Braftm1Wds/Braftm1Wds Raf1tm2Bacc/Raf1tm2Bacc
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal axon extension
|
J:121660
|
Braftm1Zim/Braftm1Zim
(involves: 129)
|
abnormal apoptosis
|
J:41257
|
Braftm2.1Urr/Braftm2.1Urr Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
impaired neuron differentiation
|
J:199842
|
increased neuronal precursor proliferation
|
J:199842
|
Braftm2Cpri/Braf+
(involves: C57BL/6)
|
cellular phenotype
|
J:187371
|
Braftm2Cpri/Braf+ Krastm4Tyj/Kras+
(involves: 129S4/SvJae * C57BL/6)
|
increased fibroblast proliferation
|
J:187371
|
Braftm2Urr/Braftm2Urr Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
abnormal neuronal precursor proliferation
|
J:199842
|
impaired neuron differentiation
|
J:199842
|
Braptm1.1Yfng/Braptm1.1Yfng
(involves: C57BL/6 * FVB/N)
|
abnormal mitosis
|
J:197131
|
Braptm1.1Yfng/Braptm1.1Yfng Pafah1b1tm1Awb/Pafah1b1+
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N)
|
abnormal mitosis
|
J:197131
|
Brca1tm1Bhk/Brca1+
(C.129P2-Brca1tm1Bhk)
|
decreased mammary gland epithelial cell proliferation
|
J:198018
|
early cellular replicative senescence
|
J:198018
|
Brca1tm1Brn/Brca1tm1Brn
(involves: 129P2/OlaHsd)
|
abnormal cell death
|
J:117113
|
decreased cell proliferation
|
J:117113
|
Brca1tm1Brn/Brca1tm1Brn Trp53tm1Brn/Trp53tm1Brn
(involves: 129P2/OlaHsd)
|
increased cell proliferation
|
J:117113
|
Brca1tm1Cxd/Brca1tm1Cxd
(either: 129S6/SvEvTac-Brca1tm1Cxd or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6))
|
abnormal chromosome number
|
J:51834
|
increased cellular sensitivity to gamma-irradiation
|
J:51834
|
Brca1tm1Cxd/Brca1tm1Cxd
(involves: 129S6/SvEvTac)
|
abnormal double-strand DNA break repair
|
J:269823
|
Brca1tm1Cxd/Brca1tm1Cxd Trp53tm1Brd/Trp53tm1Brd
(involves: 129S6/SvEvTac * 129S7/SvEvBrd)
|
abnormal chromosome number
|
J:51834
|
spontaneous chromosome breakage
|
J:51834
|
Brca1tm1Cxd/Brca1tm2Cxd Tg(KRT5-cre)5132Jlj/0
(involves: 129S6/SvEvTac * C57BL/6)
|
increased keratinocyte proliferation
|
J:85354
|
Brca1tm1Cxd/Brca1tm2Cxd Tg(KRT5-cre)5132Jlj/0 Tg(KRT5-E2F1)2Dgj/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased keratinocyte proliferation
|
J:85354
|
Brca1tm1Cxd/Brca1tm2Cxd Tg(KRT5-E2F1)2Dgj/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased keratinocyte proliferation
|
J:85354
|
Brca1tm1Rfo/Brca1tm1Rfo
(involves: 129P2/OlaHsd)
|
increased apoptosis
|
J:69602
|
Brca1tm1Whl/Brca1tm1Whl
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cell proliferation
|
J:34458
|
Brca1tm2.1Cxd/Brca1tm2.1Cxd
(involves: 129S6/SvEvTac)
|
abnormal cell adhesion
|
J:134494
|
abnormal cell death
|
J:70271
|
abnormal cell migration
|
J:134494
|
chromosomal instability
|
J:307190
|
increased apoptosis
|
J:70271
|
increased cellular sensitivity to gamma-irradiation
|
J:81541
|
Brca1tm2.1Cxd/Brca1tm2.1Cxd
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal centrosome morphology
|
J:177853
|
decreased fibroblast proliferation
|
J:177853
|
early cellular replicative senescence
|
J:177853
|
Brca1tm2.1Cxd/Brca1tm2.1Cxd Gadd45atm1Ajf/Gadd45atm1Ajf
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * C57BL/6)
|
abnormal centrosome morphology
|
J:91673
|
aneuploidy
|
J:91673
|
Brca1tm2.1Cxd/Brca1tm2.1Cxd Parp1tm1Zqw/Parp1tm1Zqw
(involves: 129S2/SvPas * 129S6/SvEvTac)
|
abnormal centrosome morphology
|
J:139260
|
abnormal chromosome morphology
|
J:139260
|
aneuploidy
|
J:139260
|
decreased cell proliferation
|
J:139260
|
decreased telomere length
|
J:139260
|
Brca1tm2.1Cxd/Brca1tm2.1Cxd Shld1em1Nus/Shld1em1Nus
(involves: 129S6/SvEvTac * C57BL/6NCrl)
|
chromosomal instability
|
J:307190
|
Brca1tm2.1Cxd/Brca1tm2.1Cxd Trp53tm1Brd/Trp53+
(involves: 129S6/SvEvTac * 129S7/SvEvBrd)
|
abnormal cell cycle checkpoint function
|
J:70271
|
increased embryonic tissue cell apoptosis
|
J:70271
|
increased fibroblast proliferation
|
J:70271
|
Brca1tm2.1Cxd/Brca1tm2.1Cxd Trp53tm1Brd/Trp53+
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB)
|
abnormal male meiosis
|
J:82308
|
arrest of male meiosis
|
J:82308
|
azoospermia
|
J:82308
|
decreased cell proliferation
|
J:81559
|
decreased spermatid number
|
J:82308
|
increased male germ cell apoptosis
|
J:82308
|
meiotic nondisjunction
|
J:82308
|
Brca1tm2.1Cxd/Brca1tm2.1Cxd Trp53bp1tm1Jc/Trp53bp1tm1Jc
(involves: 129 * 129S6/SvEvTac)
|
chromosomal instability
|
J:307190
|
Brca1tm2Arge/Brca1tm2Arge
(involves: 129)
|
abnormal double-strand DNA break repair
|
J:194229
|
Brca1tm2Cxd/Brca1+ Tg(KRT5-E2F1)2Dgj/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased keratinocyte proliferation
|
J:85354
|
Brca1tm2Cxd/Brca1tm2Cxd Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * 129S6/SvEvTac)
|
chromosome breakage
|
J:197442
|
Brca1tm2Cxd/Brca1tm2Cxd Tg(MMTV-cre)4Mam/0
(involves: 129S6/SvEvTac * C57BL/6 * FVB)
|
increased mammary gland epithelial cell proliferation
|
J:132088
|
Brca1tm2Cxd/Brca1tm2Cxd Trp53tm1Brd/Trp53+ Tg(MMTV-cre)4Mam/0
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB)
|
increased mammary gland epithelial cell proliferation
|
J:132088
|
Brca1tm2Cxd/Brca1tm2Cxd Trp53bp1tm1Jc/Trp53bp1tm1Jc Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * 129S6/SvEvTac)
|
cellular phenotype
|
J:197442
|
Brca1tm2Mak/Brca1tm2Mak Chek2tm1Mak/Chek2tm1Mak Tg(Lck-cre)548Jxm/?
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
cellular phenotype
|
J:90512
|
chromosomal instability
|
J:90512
|
Brca1tm2Mak/Brca1tm2Mak Tg(BCL2)36Wehi/? Tg(Lck-cre)548Jxm/?
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
chromosomal instability
|
J:63282
|
spontaneous chromosome breakage
|
J:63282
|
Brca1tm2Mak/Brca1tm2Mak Tg(Lck-cre)548Jxm/?
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal cell cycle checkpoint function
|
J:63282
|
abnormal cell death
|
J:63282
|
decreased T cell proliferation
|
J:63282
|
increased cellular sensitivity to gamma-irradiation
|
J:63282
|
Brca1tm2Mak/Brca1tm2Mak Tg(Lck-cre)548Jxm/? Tg(TcrLCMV)327Sdz/?
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased T cell proliferation
|
J:63282
|
Brca1tm2Mak/Brca1tm2Mak Tg(Lck-cre)548Jxm/? Trp53tm1Brd/Trp53tm1Brd
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
chromosomal instability
|
J:63282
|
spontaneous chromosome breakage
|
J:63282
|
Brca1tm2Rjbr/Brca1tm2Rjbr
(involves: 129 * C57BL/6)
|
abnormal centrosome morphology
|
J:177853
|
decreased fibroblast proliferation
|
J:177853
|
early cellular replicative senescence
|
J:177853
|
Brca1tm3.1Rjbr/Brca1tm3.1Rjbr
(involves: 129 * C57BL/6)
|
azoospermia
|
J:177853
|
cellular phenotype
|
J:177853
|
Brca1tm3Cxd/Brca1tm3Cxd
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal cell cycle
|
J:94114
|
Brca1tm4Cxd/Brca1tm4Cxd
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
abnormal cell cycle
|
J:112308
|
abnormal centrosome morphology
|
J:112308
|
Brca1tm5.1Cxd/Brca1tm5.1Cxd
(involves: 129S6/SvEvTac * FVB/N)
|
increased cellular sensitivity to gamma-irradiation
|
J:155810
|
increased mammary gland epithelial cell proliferation
|
J:155810
|
Brca2tm1Brn/Brca2tm1Brn Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd)
|
chromosome breakage
|
J:197442
|
Brca2tm1Brn/Brca2tm1Brn Trp53bp1tm1Jc/Trp53bp1tm1Jc Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd)
|
chromosome breakage
|
J:197442
|
Brca2tm1Cam/Brca2tm1Brn Krastm4Tyj/Kras+ Tg(Pdx1-cre)6Tuv/0
(involves: 129P2/OlaHsd * 129S/SvEv * 129S4/SvJae * C57BL/6 * FVB/N)
|
increased pancreas apoptosis
|
J:166678
|
Brca2tm1Cam/Brca2tm1Cam
(involves: 129S/SvEv * MF1)
|
absent germ cells
|
J:46812
|
Brca2tm1Cam/Brca2tm1Cam
(involves: 129S/SvEv)
|
abnormal mitosis
|
J:93261
|
Brca2tm1Cbl/Brca2tm1Cbl
(either: (involves: 129S2/SvPas * C57BL/10) or (involves: 129S2/SvPas * C57BL/6 * DBA/2))
|
abnormal double-strand DNA break repair
|
J:44386
|
azoospermia
|
J:44386
|
decreased fibroblast proliferation
|
J:44386
|
Brca2tm1Hst/Brca2tm2Hst
(involves: 129S7/SvEvBrd * C57BL/6)
|
chromosomal instability
|
J:82434
|
early cellular replicative senescence
|
J:82434
|
Brca2tm1Kamc/Brca2tm1Kamc
(involves: 129P2/OlaHsd * BALB/c)
|
abnormal chromosome morphology
|
J:144998
|
abnormal DNA repair
|
J:144998
|
increased sensitivity to induced cell death
|
J:144998
|
Brca2tm1Kamc/Brca2tm1Kamc Swsap1em1Mjn/Swsap1em1Mjn
(involves: 129P2/OlaHsd * C57BL/6J * CBA/J)
|
abnormal chromosomal synapsis
|
J:268570
|
arrest of male meiosis
|
J:268570
|
Brca2tm1Mak/Brca2tm2Mak Tg(Lck-cre)548Jxm/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal chromosome morphology
|
J:79697
|
aneuploidy
|
J:79697
|
cellular phenotype
|
J:79697
|
increased T cell apoptosis
|
J:79697
|
Brca2tm1Mak/Brca2tm2Mak Trp53tm1Brd/Trp53tm1Brd Tg(Lck-cre)548Jxm/0
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * CBA)
|
abnormal chromosome morphology
|
J:79697
|
decreased cellular sensitivity to ionizing radiation
|
J:79697
|
Brca2tm1Mhun/Brca2+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal cell physiology
|
J:89083
|
increased apoptosis
|
J:89083
|
Brd1tm1Hko/Brd1tm1Hko
(B6.129-Brd1tm1Hko)
|
increased apoptosis
|
J:177092
|
Brd2Gt(RRE050)Byg/Brd2+
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cell proliferation
|
J:147040
|
Brd2Gt(RRE050)Byg/Brd2Gt(RRE050)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle
|
J:147040
|
abnormal cell death
|
J:147040
|
decreased cell proliferation
|
J:147040
|
increased embryonic tissue cell apoptosis
|
J:147040
|
Brd7tm1.2Ligy/Brd7tm1.2Ligy
(involves: 129S4/SvJaeSor * C57BL/6J * FVB/N)
|
abnormal acrosome morphology
|
J:251649
|
abnormal sperm head morphology
|
J:251649
|
abnormal spermatid morphology
|
J:251649
|
absent acrosome
|
J:251649
|
azoospermia
|
J:251649
|
globozoospermia
|
J:251649
|
increased male germ cell apoptosis
|
J:251649
|
Brdttm1a(EUCOMM)Wtsi/Brdttm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
arrest of male meiosis
|
J:190041
|
Brdttm1a(EUCOMM)Wtsi/Brdttm1a(EUCOMM)Wtsi
(C57BL/6-Brdttm1a(EUCOMM)Wtsi)
|
abnormal spermatid morphology
|
J:232496
|
abnormal spermatocyte morphology
|
J:232496
|
arrest of male meiosis
|
J:232496
|
azoospermia
|
J:232496
|
decreased round spermatid number
|
J:232496
|
increased male germ cell apoptosis
|
J:232496
|
Brdttm1Djw/Brdttm1Djw
(involves: 129S/SvEv * C57BL/6J)
|
abnormal acrosome assembly
|
J:128000
|
abnormal sperm flagellum morphology
|
J:128000
|
abnormal sperm head morphology
|
J:128000
|
abnormal sperm midpiece morphology
|
J:128000
|
abnormal spermatid morphology
|
J:128000
|
asthenozoospermia
|
J:128000
|
oligozoospermia
|
J:128000
|
teratozoospermia
|
J:128000
|
Brf1tm1Arte/Brf1tm1Arte Tg(Cyp1a1-cre)1Dwi/0
(involves: C57BL/6 * CBA)
|
abnormal translation
|
J:285667
|
increased hepatocyte apoptosis
|
J:285667
|
Brinp1tm1Imts/Brinp1tm1Imts
(B6J.Cg-Brinp1tm1Imts)
|
impaired neuron differentiation
|
J:221295
|
Brip1Gt(RRI409)Byg/Brip1Gt(RRI409)Byg
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:227115,
J:227337
|
abnormal chiasmata formation
|
J:227337
|
abnormal chromosome morphology
|
J:227115
|
abnormal DNA replication
|
J:227115
|
abnormal double-strand DNA break repair
|
J:227115,
J:227337
|
abnormal spermatogonia proliferation
|
J:227337
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:227337
|
chromosomal instability
|
J:227115
|
decreased cell proliferation
|
J:227337
|
decreased primordial germ cell number
|
J:227337
|
decreased primordial germ cell proliferation
|
J:227337
|
decreased spermatogonia number
|
J:227115
|
early cellular replicative senescence
|
J:227115
|
increased cellular sensitivity to DNA damaging agents
|
J:227115
|
increased primordial germ cell apoptosis
|
J:227337
|
induced chromosome breakage
|
J:227115
|
oligozoospermia
|
J:227337
|
Brip1Gt(RRI409)Byg/Brip1Gt(RRI409)Byg Fancd2tm1Hou/Fancd2tm1Hou
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
increased cellular sensitivity to DNA damaging agents
|
J:227115
|
Brk1Gt(DC0002)Wtsi/Brk1Gt(DC0002)Wtsi
(involves: 129P2/OlaHsd)
|
abnormal actin cytoskeleton morphology
|
J:166082
|
Brme1em1Amp/Brme1em1Amp
(involves: C57BL/6J * CBA/J)
|
abnormal chromosomal synapsis
|
J:303558
|
abnormal male meiosis
|
J:303558
|
azoospermia
|
J:303558
|
Brme1em1Hirok/Brme1em1Hirok
(C57BL/6J-Brme1em1Hirok)
|
abnormal chiasmata formation
|
J:292036
|
abnormal chromosomal synapsis
|
J:292036
|
abnormal double-strand DNA break repair
|
J:292036
|
abnormal male meiosis
|
J:292036
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:292036
|
azoospermia
|
J:292036
|
increased male germ cell apoptosis
|
J:292036
|
Brme1em1Zhal/Brme1em1Zhal
(involves: C57BL/6)
|
abnormal double-strand DNA break repair
|
J:291221
|
abnormal male meiosis
|
J:291221
|
abnormal spermatocyte morphology
|
J:291221
|
azoospermia
|
J:291221
|
decreased elongated spermatid number
|
J:291221
|
decreased round spermatid number
|
J:291221
|
decreased spermatid number
|
J:291221
|
increased male germ cell apoptosis
|
J:291221
|
Brpf1tm1c(EUCOMM)Wtsi/Brpf1tm1c(EUCOMM)Wtsi Commd10Tg(Vav1-icre)A2Kio/Commd10+
(involves: C57BL/6J * C57BL/6N * C57BL/10 * CBA/Ca)
|
abnormal cell physiology
|
J:240552
|
Brpf1tm1c(EUCOMM)Wtsi/Brpf1tm1c(EUCOMM)Wtsi Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas * C57BL/6J * C57BL/6N)
|
abnormal cell cycle checkpoint function
|
J:224155
|
abnormal cell physiology
|
J:240552
|
abnormal neuronal precursor cell migration
|
J:224155
|
abnormal radial glial cell morphology
|
J:224155
|
decreased neuronal precursor proliferation
|
J:224155,
J:241490
|
decreased radial glial cell number
|
J:224155
|
Brpf1tm1d(EUCOMM)Wtsi/Brpf1+
(involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N)
|
abnormal cell physiology
|
J:240552
|
Brpf1tm1d(EUCOMM)Wtsi/Brpf1tm1d(EUCOMM)Wtsi
(involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N)
|
abnormal cell physiology
|
J:240552
|
Brpf3tm1b(EUCOMM)Wtsi/Brpf3tm1b(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N * FVB/N)
|
cellular phenotype
|
J:231042
|
Brpf3tm1d(EUCOMM)Wtsi/Brpf3tm1d(EUCOMM)Wtsi
(involves: C3H * C57BL/6J * C57BL/6N * FVB/N)
|
cellular phenotype
|
J:231042
|
Brsk1tm1Jrs/Brsk1tm1Jrs Brsk2tm1Jrs/Brsk2tm1Jrs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal axon extension
|
J:96030
|
Brsk2tm2.1Jrs/Brsk2tm2.1Jrs Isl1tm1(cre)Tmj/Isl1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal axon extension
|
J:201695
|
Brwd1Gt(AW0417)Wtsi/Brwd1Gt(AW0417)Wtsi
(involves: 129P2/OlaHsd)
|
abnormal female meiosis
|
J:136078
|
abnormal male germ cell morphology
|
J:136078
|
decreased male germ cell number
|
J:136078
|
Brwd1Gt(AW0417)Wtsi/Brwd1repro5
(involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:136078
|
decreased male germ cell number
|
J:136078
|
globozoospermia
|
J:136078
|
Brwd1repro5/Brwd1repro5
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal female meiosis
|
J:136078
|
abnormal male germ cell morphology
|
J:136078
|
abnormal oocyte morphology
|
J:92463
|
abnormal sperm flagellum morphology
|
J:136078
|
abnormal sperm head morphology
|
J:136078
|
abnormal sperm midpiece morphology
|
J:136078
|
asthenozoospermia
|
J:92463,
J:136078
|
globozoospermia
|
J:92463,
J:136078
|
necrospermia
|
J:136078
|
oligozoospermia
|
J:92463
|
teratozoospermia
|
J:136078
|
Bscl2tm1.1Gliu/Bscl2tm1.1Gliu Tg(Ddx4-cre)1Dcas/0
(involves: 129 * 129S4/SvJaeSor * FVB/N)
|
abnormal male germ cell morphology
|
J:211072
|
abnormal sperm flagellum morphology
|
J:211072
|
abnormal sperm head morphology
|
J:211072
|
abnormal spermatid morphology
|
J:211072
|
asthenozoospermia
|
J:211072
|
oligozoospermia
|
J:211072
|
teratozoospermia
|
J:211072
|
Bscl2tm1.1Lchan/Bscl2tm1.1Lchan
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal aerobic respiration
|
J:183701
|
abnormal cellular respiration
|
J:183701
|
abnormal fat cell differentiation
|
J:183701
|
Bscl2tm1.2Gliu/Bscl2tm1.2Gliu
(involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N)
|
abnormal male germ cell morphology
|
J:211072
|
abnormal sperm flagellum morphology
|
J:211072
|
abnormal sperm head morphology
|
J:211072
|
abnormal spermatid morphology
|
J:211072
|
abnormal white fat cell differentation
|
J:173404
|
asthenozoospermia
|
J:211072
|
decreased round spermatid number
|
J:211072
|
oligozoospermia
|
J:211072
|
teratozoospermia
|
J:211072
|
Bsgtm1.1Znc/Bsgtm1.1Znc Tg(Lck-cre)19Hhan/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA)
|
increased T cell proliferation
|
J:207886
|
Bsgtm1Tmu/Bsgtm1Tmu
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal spermatocyte morphology
|
J:199573
|
arrest of male meiosis
|
J:46376
|
azoospermia
|
J:199573,
J:46376
|
decreased male germ cell number
|
J:199573
|
increased male germ cell apoptosis
|
J:199573
|
multinucleated giant male germ cells
|
J:199573
|
Bsgtm1Tmu/Bsgtm1Tmu
(involves: 129/Sv * 129S2/SvPas)
|
arrest of male meiosis
|
J:46376
|
azoospermia
|
J:46376
|
Bsgtm1Tmu/Bsgtm1Tmu
(involves: 129S2/SvPas)
|
increased mesangial cell number
|
J:287636
|
Bst2tm1.1Bsz/Bst2tm1.1Bsz
(involves: C57BL/6)
|
abnormal cell physiology
|
J:180252
|
Bsxtm1Aoh/Bsxtm1Aoh
(either: 129S4/SvJae-Bsxtm1Aoh or (involves: 129S4/SvJae * C57BL/6))
|
maternal effect
|
J:123638
|
Bsxtm2Aoh/Bsxtm2Aoh
(either: 129S4/SvJae-Bsxtm2Aoh or (involves: 129S4/SvJae * C57BL/6))
|
maternal effect
|
J:123638
|
Btbd7tm1.1Kmy/Btbd7tm1.1Kmy
(involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J)
|
decreased cell migration
|
J:241996
|
Btbd8em1Lych/Btbd8em1Lych
(involves: C57BL/6)
|
increased colon goblet cell number
|
J:349252
|
Btbd18tm1Dean/Btbd18tm1Dean
(involves: 129S4/SvJae * C57BL/6)
|
azoospermia
|
J:240025
|
decreased male germ cell number
|
J:240025
|
decreased round spermatid number
|
J:240025
|
increased male germ cell apoptosis
|
J:240025
|
increased testis apoptosis
|
J:240025
|
Btg1tm1Ftir/Btg1tm1Ftir
(Not Specified)
|
decreased neuronal precursor proliferation
|
J:217516
|
increased neuron apoptosis
|
J:217516
|
Btg4em1Hyfn/Btg4em1Hyfn
(involves: ICR)
|
maternal effect
|
J:245369
|
Btg4em1Hyfn/Btg4em3Hyfn
(Not Specified)
|
maternal effect
|
J:245369
|
Btg4em2Hyfn/Btg4em2Hyfn
(involves: ICR)
|
maternal effect
|
J:245369
|
Btktm1Gsv/Y Tg(CD19-BTK*K430R)XK24Rwhe/?
(involves: 129P2/OlaHsd * C57BL/6 * FVB)
|
decreased B cell apoptosis
|
J:120989
|
Btktm1Wk/Btktm1Wk
(involves: 129S4/SvJae * C57BL/6)
|
decreased B cell proliferation
|
J:82298
|
Btktm1Wk/Btktm1Wk Cd40tm1Geha/Cd40tm1Geha
(involves: 129S4/SvJae * C57BL/6)
|
decreased B cell proliferation
|
J:82298
|
Btktm1Wk/Btktm1Wk Tectm1Welm/Tectm1Welm
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:66080
|
Btktm1Wk/Btktm1Wk Tg(IGH-Btk)1Witt/0
(involves: 129S4/SvJae * 129X1/SvJ * BALB/c * C3H * C57BL/6)
|
decreased B cell proliferation
|
J:82430
|
Btkxid/Y
(CBA/HN-Btkxid)
|
decreased B cell proliferation
|
J:81429
|
Btkxid/Y
(involves: CBA/HN * DBA/2N)
|
decreased B cell proliferation
|
J:81429
|
Btkxid/?
(involves: BALB/c * CBA/N)
|
decreased B cell proliferation
|
J:108696
|
Btkxid/? Ptpn6me/Ptpn6me
(involves: C57BL/6J * CBA/N * NFS)
|
increased splenocyte proliferation
|
J:30994
|
Btkxid/? Tg(IGH-Btk)1Witt/0
(involves: BALB/c * C3H * C57BL/6 * CBA/N)
|
decreased B cell proliferation
|
J:108696
|
Btkxid/? Tg(IGH-Btk)1Witt/Tg(IGH-Btk)1Witt
(involves: BALB/c * C3H * C57BL/6 * CBA/N)
|
decreased B cell proliferation
|
J:108696
|
Btkxid/Btkxid
(CBA/CaHN-Btkxid/J)
|
impaired neutrophil phagocytosis
|
J:92639
|
Btkxid/Btkxid
(involves: CBA/HN * DBA/2N)
|
abnormal B cell proliferation
|
J:81429
|
Btkxid/Btkxid
(CBA/HN-Btkxid)
|
decreased B cell proliferation
|
J:81429
|
Btlatm1Kmm/Btlatm1Kmm
(involves: 129S/SvEv)
|
increased B cell proliferation
|
J:84084
|
increased T cell proliferation
|
J:84084
|
Btlatm1Kmm/Btlatm1Kmm
(B6.129S-Btlatm1Kmm)
|
decreased T cell proliferation
|
J:119356
|
increased T cell proliferation
|
J:119356
|
Btlatm1Kmm/Btlatm1Kmm Pdcd1tm1Hon/Pdcd1tm1Hon
(B6.129S-Pdcd1tm1Hon Btlatm1Kmm)
|
increased T cell proliferation
|
J:119356
|
Btlatm1Kmm/Btlatm1Kmm Tg(DO11.10)10Dlo/?
(involves: 129S/SvEv * BALB/c * C3H * C57BL/6)
|
increased T cell proliferation
|
J:84084
|
Btrctm1Kin/Btrctm1Kin
(involves: C57BL/6)
|
abnormal cell morphology
|
J:84639
|
decreased fibroblast proliferation
|
J:84639
|
increased fibroblast apoptosis
|
J:84639
|
polyploidy
|
J:84639
|
Btrctm1Paga/Btrctm1Paga
(involves: 129S2/SvPas)
|
abnormal centrosome morphology
|
J:93010
|
abnormal male meiosis
|
J:93010
|
abnormal meiotic spindle morphology
|
J:93010
|
abnormal mitosis
|
J:93010
|
abnormal mitotic spindle morphology
|
J:93010
|
oligozoospermia
|
J:93010
|
Btrctm1Paga/Btrctm1Paga Fbxw11tm1Ybn/Fbxw11tm1Ybn Tg(Vil1-cre/ERT2)23Syr/?
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal centrosome morphology
|
J:206654
|
abnormal mitosis
|
J:206654
|
abnormal mitotic spindle morphology
|
J:206654
|
chromosomal instability
|
J:206654
|
Bub1Gt(XG453)Byg/Bub1+
(involves: 129P2/OlaHsd * C57BL/6J)
|
maternal effect
|
J:143035
|
Bub1tm1.1Jvd/Bub1+
(involves: 129/Sv * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:135093
|
abnormal mitosis
|
J:135093
|
aneuploidy
|
J:135093
|
decreased fibroblast apoptosis
|
J:135093
|
Bub1tm1.1Jvd/Bub1tm2Jvd
(involves: 129/Sv * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:135093
|
abnormal mitosis
|
J:135093
|
aneuploidy
|
J:135093
|
decreased fibroblast apoptosis
|
J:135093
|
Bub1tm1.1Tvd/Bub1+
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J)
|
aneuploidy
|
J:143035
|
Bub1tm1.1Tvd/Bub1tm1.1Tvd
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J)
|
abnormal cell cycle
|
J:143035
|
abnormal cell cycle checkpoint function
|
J:143035
|
abnormal mitotic spindle assembly checkpoint
|
J:143035
|
abnormal mitotic spindle morphology
|
J:143035
|
aneuploidy
|
J:143035
|
decreased fibroblast proliferation
|
J:143035
|
early cellular replicative senescence
|
J:143035
|
Bub1tm1Ssta/Bub1tm1.1Ssta Tg(CAG-cre/Esr1*)5Amc/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal cell cycle
|
J:128455
|
abnormal mitotic spindle assembly checkpoint
|
J:128455
|
decreased cell proliferation
|
J:128455
|
Bub1tm1Ssta/Bub1tm1Ssta Tg(CAG-cre/Esr1*)5Amc/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased mitotic index
|
J:128455
|
oligozoospermia
|
J:128455
|
Bub1tm2Jvd/Bub1+
(involves: 129/Sv * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:135093
|
abnormal mitosis
|
J:135093
|
aneuploidy
|
J:135093
|
decreased fibroblast apoptosis
|
J:135093
|
Bub1tm2Jvd/Bub1tm2Jvd
(involves: 129/Sv * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:135093
|
abnormal mitosis
|
J:135093
|
aneuploidy
|
J:135093
|
decreased fibroblast apoptosis
|
J:135093
|
Bub1tm3.1Jvd/Bub1tm3.1Jvd
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:195237
|
aneuploidy
|
J:195237
|
chromosomal instability
|
J:195237
|
oligozoospermia
|
J:195237
|
Bub1tm4.1Jvd/Bub1tm4.1Jvd
(involves: 129S4/SvJaeSor)
|
abnormal cell death
|
J:195237
|
Bub1bGt(neo-btk)1Dai/Bub1b+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:88223
|
Bub1bGt(neo-btk)1Dai/Bub1b+
(involves: 129S4/SvJae)
|
abnormal mitotic spindle assembly checkpoint
|
J:88094
|
Bub1bGt(neo-btk)1Dai/Bub1bGt(neo-btk)1Dai
(involves: 129S4/SvJae * C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:88223
|
Bub1btm1.1Hsl/Bub1b+
(involves: 129 * C57BL/6)
|
increased B cell proliferation
|
J:201641
|
Bub1btm1.1Hsl/Bub1b+ Tg(HIST1H2BB/EGFP)1Pa/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell nucleus morphology
|
J:201641
|
abnormal mitosis
|
J:201641
|
abnormal mitotic spindle assembly checkpoint
|
J:201641
|
aneuploidy
|
J:201641
|
Bub1btm1.1Hsl/Bub1btm1.1Hsl
(involves: 129 * C57BL/6)
|
increased apoptosis
|
J:201641
|
Bub1btm1.1Jvd/Bub1b+
(involves: 129S6/SvEvTac)
|
abnormal cell cycle checkpoint function
|
J:105717
|
Bub1btm1.1Jvd/Bub1b+
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal mitosis
|
J:293084
|
abnormal mitotic spindle assembly checkpoint
|
J:293084
|
aneuploidy
|
J:293084
|
Bub1btm1Jvd/Bub1b+
(involves: 129S6/SvEvTac)
|
abnormal cell cycle checkpoint function
|
J:105717
|
Bub1btm1Jvd/Bub1btm1Jvd
(involves: 129S6/SvEvTac)
|
abnormal cell cycle checkpoint function
|
J:105717
|
abnormal cell physiology
|
J:91128
|
abnormal cellular replicative senescence
|
J:105717,
J:91128
|
abnormal mitosis
|
J:105717
|
chromosome breakage
|
J:91128
|
oligozoospermia
|
J:91128
|
Bub1btm1Jvd/Bub1btm1Jvd
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal mitosis
|
J:293084
|
abnormal mitotic spindle assembly checkpoint
|
J:293084
|
abnormal mitotic spindle morphology
|
J:293084
|
aneuploidy
|
J:293084
|
early cellular replicative senescence
|
J:293084
|
Bub1btm1Jvd/Bub1btm1Jvd
(involves: 129S6/SvEvTac * C57BL/6 * FVB)
|
aneuploidy
|
J:234643
|
Bub1btm1Jvd/Bub1btm1Jvd Mad2l1bptm1.1Itl/Mad2l1bptm1.1Itl Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * FVB)
|
increased hepatocyte karyomegaly
|
J:234643
|
polyploidy
|
J:234643
|
Bub1btm1Jvd/Bub1btm2.1Jvd
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal mitosis
|
J:293084
|
abnormal mitotic spindle assembly checkpoint
|
J:293084
|
abnormal mitotic spindle morphology
|
J:293084
|
aneuploidy
|
J:293084
|
Bub1btm1Jvd/Bub1btm3.1Jvd
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal mitosis
|
J:293084
|
abnormal mitotic spindle assembly checkpoint
|
J:293084
|
abnormal mitotic spindle morphology
|
J:293084
|
aneuploidy
|
J:293084
|
early cellular replicative senescence
|
J:293084
|
Bub1btm2.1Jvd/Bub1b+
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6)
|
abnormal mitosis
|
J:194926
|
aneuploidy
|
J:194926
|
early cellular replicative senescence
|
J:194926
|
Bub1btm2.1Jvd/Bub1b+
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal chromosome number
|
J:293084
|
abnormal mitosis
|
J:293084
|
abnormal mitotic spindle assembly checkpoint
|
J:293084
|
abnormal mitotic spindle morphology
|
J:293084
|
aneuploidy
|
J:293084
|
Bub1btm3.1Jvd/Bub1b+
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal chromosome number
|
J:293084
|
abnormal mitosis
|
J:293084
|
abnormal mitotic spindle assembly checkpoint
|
J:293084
|
abnormal mitotic spindle morphology
|
J:293084
|
aneuploidy
|
J:293084
|
Bub3tm1Jvd/Bub3+
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:81546,
J:105717
|
abnormal mitosis
|
J:81546,
J:105717
|
aneuploidy
|
J:81546,
J:105717
|
Bub3tm1Jvd/Bub3+ Rae1tm1Jvd/Rae1+
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:105717
|
abnormal cellular replicative senescence
|
J:105717
|
abnormal mitosis
|
J:81546,
J:105717
|
aneuploidy
|
J:81546,
J:105717
|
decreased cell proliferation
|
J:81546
|
Bub3tm1Khac/Bub3tm1Khac
(either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv))
|
abnormal cell nucleus morphology
|
J:64874
|
abnormal chromosome morphology
|
J:64874
|
Bud23em1Asil/Bud23+
(involves: C57BL/6 * DBA/2)
|
abnormal oxidative phosphorylation
|
J:290738
|
increased mitochondrial number
|
J:290738
|
Bud23em2Asil/Bud23em2Asil Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6 * C57BL/6J * DBA/2)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:290738
|
abnormal mitochondrial morphology
|
J:290738
|
abnormal oxidative phosphorylation
|
J:290738
|
decreased mitochondrial number
|
J:290738
|
decreased myocardial fiber mitochondrial DNA content
|
J:290738
|
oxidative stress
|
J:290738
|
bumpy/bumpy Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw
(involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal axon extension
|
J:168258
|
abnormal axon fasciculation
|
J:168258
|
C1galt1tm1.1Rpmc/C1galt1tm1.1Rpmc Mgat1tm2Jxm/Mgat1tm2Jxm Tg(Zp3-cre)1Gwh/?
(involves: 129S1/Sv * 129S1/SvImJ * 129X1/SvJ * C57BL/6)
|
decreased oocyte number
|
J:122012
|
C1galt1tm1.1Rpmc/C1galt1tm1.1Rpmc Mgat1tm2Jxm/Mgat1tm2Jxm Tg(Zp3-cre)1Gwh/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal zona pellucida morphology
|
J:173879
|
C1galt1tm1.1Staka/C1galt1tm1.2Staka Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * C57BL/6J * CBA * DBA/2)
|
abnormal megakaryocyte differentiation
|
J:202276
|
C1galt1tm1.2Rpmc/C1galt1tm1.2Rpmc
(involves: 129S1/Sv * 129S1/SvImJ * C57BL/6)
|
abnormal zona pellucida morphology
|
J:122012
|
thin zona pellucida
|
J:122012
|
C1qatm1Mjw/C1qatm1Mjw
(involves: 129P2/Ola * 129S/SvEv * C57BL/6)
|
increased renal glomerulus apoptosis
|
J:47315
|
C1qbptm1.1Tuch/C1qbptm1.1Tuch
(involves: C57BL/6)
|
abnormal respiratory electron transport chain
|
J:196232
|
decreased cell proliferation
|
J:196232
|
C1qtnf4em1Smoc/C1qtnf4em1Smoc
(C57BL/6JSmoc-C1qtnf4em1Smoc/Smoc)
|
abnormal macrophage differentiation
|
J:302282
|
C2cd3em1Brgm/C2cd3em1Brgm
(involves: C57BL/6NCrl * CD-1)
|
abnormal primary cilium morphology
|
J:308674
|
C2cd3em2Brgm/C2cd3em2Brgm E2f1Tg(Wnt1-cre)2Sor/E2f1+
(involves: C3H * C57BL/6)
|
abnormal cilium physiology
|
J:308674
|
C2cd3Gt(AG0177)Wtsi/C2cd3Gt(AG0177)Wtsi
(involves: 129P2/OlaHsd * C3H/He)
|
absent embryonic cilia
|
J:142506
|
C2cd3hty/C2cd3hty
(involves: C3H/He * C57BL/6)
|
absent embryonic cilia
|
J:142506
|
C2cd3tm1c(EUCOMM)Wtsi/C2cd3tm1c(EUCOMM)Wtsi E2f1Tg(Wnt1-cre)2Sor/E2f1+
(involves: C3H * C57BL/6)
|
abnormal cilium physiology
|
J:308674
|
C2cd5Gt(IST12020E4)Tigm/C2cd5Gt(IST12020E4)Tigm
(C57BL/6N-C2cd5Gt(IST12020E4)Tigm)
|
decreased adipocyte glucose uptake
|
J:284780
|
decreased cardiac muscle cell glucose uptake
|
J:284780
|
decreased fatty acid oxidation
|
J:284780
|
decreased skeletal muscle cell glucose uptake
|
J:284780
|
C2cd6tm1Jw/C2cd6tm1Jw
(involves: 129S4/SvJae * C57BL/6)
|
abnormal sperm flagellum morphology
|
J:316788
|
decreased hyperactivated sperm motility
|
J:316788
|
C3tm1Crr/C3tm1Crr
(involves: 129S4/SvJae * C57BL/6)
|
decreased hepatocyte proliferation
|
J:152533
|
C3tm1Crr/C3tm1Crr Cd59atm1Bpm/Cd59atm1Bpm
(B6.129-Cd59atm1Bpm C3tm1Crr)
|
increased T cell proliferation
|
J:122201
|
C3tm1Crr/C3tm1Crr Tg(Ins2-TFRC/OVA)296Wehi/0
(involves: 129S4/SvJae * C57BL/6)
|
increased T cell proliferation
|
J:122114
|
C3ar1tm1Cge/C3ar1tm1Cge
(B6.129S4(C)-C3ar1tm1Cge)
|
increased retina apoptosis
|
J:214214
|
C3ar1tm1Cge/C3ar1tm1Cge C5ar1tm1Cge/C5ar1tm1Cge
(B6.Cg-C3ar1tm1Cge C5ar1tm1Cge)
|
increased retina apoptosis
|
J:214214
|
C5ar2tm1Gdy/C5ar2tm1Gdy
(involves: 129 * C57BL/6)
|
abnormal cellular respiration
|
J:123294
|
increased fatty acid oxidation
|
J:123294
|
C9orf72em5Lutzy/C9orf72em5Lutzy
(C57BL/6-C9orf72em5Lutzy)
|
lysosomal protein accumulation
|
J:101977
|
Cabcoco1em1Gaof/Cabcoco1em1Gaof
(involves: 129/SvEv * C57BL/6)
|
abnormal sperm flagellum morphology
|
J:345163
|
absent sperm flagellum
|
J:345163
|
asthenozoospermia
|
J:345163
|
coiled sperm flagellum
|
J:345163
|
oligozoospermia
|
J:345163
|
short sperm flagellum
|
J:345163
|
teratozoospermia
|
J:345163
|
Cables2tm1(KOMP)Vlcg/Cables2tm1(KOMP)Vlcg
(C57BL/6NTac-Cables2tm1(KOMP)Vlcg)
|
increased apoptosis
|
J:309963
|
Cabs1em1Ntu/Cabs1em1Ntu
(C57BL/6-Cabs1em1Ntu)
|
abnormal sperm annulus morphology
|
J:304106
|
absent sperm annulus
|
J:304106
|
asthenozoospermia
|
J:304106
|
kinked sperm flagellum
|
J:304106
|
Cabyrem1Osb/Cabyrem1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm axoneme morphology
|
J:247126
|
abnormal sperm fibrous sheath morphology
|
J:247126
|
abnormal sperm flagellum morphology
|
J:247126
|
abnormal sperm motility
|
J:247126
|
abnormal sperm principal piece morphology
|
J:247126
|
decreased activated sperm motility
|
J:247126
|
decreased sperm progressive motility
|
J:247126
|
Cacfd1tm1.1Geno/Cacfd1tm1.1Geno
(involves: 129S2/SvPas * C57BL/6J)
|
decreased cell proliferation
|
J:184968
|
increased apoptosis
|
J:184968
|
Cacna1atg-rol/Cacna1atg-rol
(involves: C57BL/6 * SIII)
|
increased apoptosis
|
J:107924
|
Cacna1atm2.1Kewa/Cacna1atm2.1Kewa
(B6.Cg-Cacna1atm2.1Kewa)
|
abnormal Purkinje cell mitochondrial morphology
|
J:190729
|
Cacna1ctm1Itl/Cacna1ctm1Itl
(B6.129S6-Cacna1ctm1Itl)
|
patent ductus arteriosus
|
J:171162
|
Cacna1dtm1Hssh/Cacna1dtm1Hssh
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal pancreatic beta cell differentiation
|
J:72316
|
decreased pancreatic beta cell proliferation
|
J:72316
|
Cacna1ftm1.1Sdie/Y
(B6.Cg-Cacna1ftm1.1Sdie/J)
|
abnormal retina apoptosis
|
J:212726
|
Cacna1ftm1.1Sdie/Cacna1ftm1.1Sdie
(B6.Cg-Cacna1ftm1.1Sdie/J)
|
abnormal retina apoptosis
|
J:212726
|
Cacna1ftm1.2Sdie/Y
(B6.Cg-Cacna1ftm1.2Sdie/J)
|
increased retina apoptosis
|
J:212726
|
Cacna1ftm1.2Sdie/Cacna1ftm1.2Sdie
(B6.Cg-Cacna1ftm1.2Sdie/J)
|
increased retina apoptosis
|
J:212726
|
Cacna1smdg/Cacna1smdg
(involves: STOCK T/t4)
|
increased skeletal muscle fiber mitochondrial size
|
J:5283
|
Cacna1stm1.1Arte/Cacna1stm1.1Arte
(involves: C57BL/6N)
|
abnormal mitochondrial physiology
|
J:235534
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:235534
|
decreased mitochondrial number
|
J:235534
|
decreased mitochondrial size
|
J:235534
|
dilated mitochondrion
|
J:235534
|
Cacng2stg/Cacng2stg
(B6C3Fe a/a-Cacng2stg)
|
abnormal neuron differentiation
|
J:15527
|
CacybpGT(OST39970)Lex/CacybpGT(OST39970)Lex
(involves: 129S5/SvEvBrd)
|
abnormal cell cycle checkpoint function
|
J:110899
|
increased fibroblast proliferation
|
J:110899
|
Cadm1Gt(Ayu21-W34)Imeg/Cadm1Gt(Ayu21-W34)Imeg
(involves: C57BL/6 * CBA/JNCrlj)
|
decreased T cell proliferation
|
J:178612
|
Cadm1tm1.2Brd/Cadm1tm1.2Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
asthenozoospermia
|
J:108386
|
oligozoospermia
|
J:108386
|
teratozoospermia
|
J:108386
|
Cadm1tm1.2Brd/Cadm1tm1.2Brd
(involves: 129S7/SvEvBrd)
|
increased pancreatic beta cell proliferation
|
J:210552
|
Cadm1tm1Momo/Cadm1tm1Momo
(involves: 129S/SvEv * C57BL/6J)
|
abnormal spermatid morphology
|
J:129496
|
asthenozoospermia
|
J:129496
|
decreased male germ cell number
|
J:129496
|
oligozoospermia
|
J:129496
|
teratozoospermia
|
J:129496
|
Cadm1tm1Momo/Cadm1tm1Momo
(involves: 129S/SvEv)
|
decreased elongated spermatid number
|
J:128950
|
Cadm1tm1Mrkm/Cadm1tm1Mrkm
(involves: 129S6/SvEvTac * C57BL/6J)
|
asthenozoospermia
|
J:108395
|
globozoospermia
|
J:108395
|
multiflagellated sperm
|
J:108395
|
oligozoospermia
|
J:108395
|
short sperm flagellum
|
J:108395
|
teratozoospermia
|
J:108395
|
Cadps2tm1Tfr/Cadps2tm1Tfr
(C57BL/6-Cadps2tm1Tfr)
|
abnormal cerebellar granule cell migration
|
J:120106
|
Cadpstm1.1Tfr/Cadpstm1.2Tfr Emx1tm1(cre)Ito/Emx1+
(B6.Cg-Emx1tm1(cre)Ito Cadpstm1.1Tfr Cadpstm1.2Tfr)
|
abnormal Golgi trans cisterna morphology
|
J:204664
|
Cadpstm1Bros/Cadps+ Cadps2tm1Bros/Cadps2tm1Bros
(Not Specified)
|
abnormal lysosome physiology
|
J:131014
|
Calb1tm1Mpin/Calb1tm1Mpin Pvalbtm1Swal/Pvalbtm1Swal
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal Purkinje cell mitochondrial morphology
|
J:113147
|
Calcatm1Rfg/Calcatm1Rfg
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal osteoblast physiology
|
J:80827
|
Calcrltm1Kmca/Calcrltm1Kmca
(129S6/SvEvTac-Calcrltm1Kmca)
|
abnormal fetal cardiomyocyte proliferation
|
J:106927
|
increased cardiomyocyte apoptosis
|
J:106927
|
Calr3tm1Osb/Calr3tm1Osb
(involves: 129S2/SvPas * C57BL/6)
|
impaired sperm migration in female genital tract
|
J:170595
|
Calrtm1.1Osb/Calrtm1.1Osb
(involves: 129S2/SvPas)
|
abnormal fibroblast physiology
|
J:250114
|
Calrtm1.2Osb/Calrtm1.1Osb Tg(Zp3-cre)93Knw/0
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal oocyte morphology
|
J:250114
|
decreased granulosa cell proliferation
|
J:250114
|
Calrtm1Star/Calrtm1Star
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL))
|
abnormal cell adhesion
|
J:73539
|
abnormal cell migration
|
J:61550
|
abnormal cell physiology
|
J:61550
|
increased cardiomyocyte apoptosis
|
J:61550
|
Camk2atm1Sva/Camk2a+
(B6.129P2-Camk2atm1Sva/J)
|
increased cell proliferation
|
J:263327
|
Camk2dtm1.1Mean/Camk2dtm1.1Mean
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N)
|
decreased apoptosis
|
J:207291
|
oxidative stress
|
J:207291
|
Camk2gtm1.1Irt/Camk2gtm1.1Irt
(involves: C57BL/6 * C57BL/6J)
|
decreased macrophage apoptosis
|
J:154647
|
Camk4tm1Arm/Camk4tm1Arm
(involves: 129 * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:70570
|
abnormal sperm head morphology
|
J:70570
|
decreased male germ cell number
|
J:70570
|
decreased spermatid number
|
J:70570
|
oligozoospermia
|
J:70570
|
teratozoospermia
|
J:70570
|
Camk4tm1Tch/Camk4tm1Tch
(B6.129X1-Camk4tm1Tch)
|
abnormal osteoclast differentiation
|
J:129599
|
Camkmttm1Rpav/Camkmttm1Rpav
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:228818
|
Camltm1Rjb/Camltm2Rjb Tg(Lck-cre)1Cwi/0
(involves: 129 * C57BL/6 * DBA/2)
|
increased T cell apoptosis
|
J:100536
|
Camptm1.1Jimw/Camptm1.1Jimw
(involves: C57BL/6)
|
abnormal cell chemotaxis
|
J:199611
|
Camsap1tm1Wem/Camsap1tm1Wem
(involves: C57BL/6J)
|
abnormal microtubule cytoskeleton morphology
|
J:296029
|
abnormal neuronal migration
|
J:296029
|
Camsap3tm1.1Ltm/Camsap3tm1.1Ltm
(involves: C57BL/6N * FVB/N)
|
abnormal microtubule cytoskeleton morphology
|
J:265916
|
Cant1tm1.2Aros/Cant1tm1.2Aros
(involves: 129 * C57BL/6J)
|
increased chondrocyte apoptosis
|
J:282272
|
increased chondrocyte proliferation
|
J:282272
|
Cap1tm1.1Mbrst/Cap1tm1.1Mbrst Cfl1tm1.1Wit/Cfl1tm1.1Wit Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
impaired neuron differentiation
|
J:333563
|
Cap1tm1.1Mbrst/Cap1tm1.1Mbrst Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
impaired neuron differentiation
|
J:333563
|
Cap2tm1a(EUCOMM)Wtsi/Cap2tm1a(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
cardiac interstitial fibrosis
|
J:234044
|
Capgtm1Djk/Capgtm1Djk
(involves: 129S4/SvJae)
|
impaired macrophage phagocytosis
|
J:86517
|
Capgtm1Djk/Capgtm1Djk
(involves: 129S4/SvJae * BALB/c * C57BL/6)
|
impaired macrophage phagocytosis
|
J:86277
|
impaired neutrophil chemotaxis
|
J:86277
|
Capgtm1Djk/Capgtm1Djk Gsntm1Djk/Gsntm1Djk
(involves: 129S4/SvJae)
|
impaired macrophage phagocytosis
|
J:86517
|
Capn1tm1Dgen/Capn1tm1Dgen
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal leukocyte adhesion
|
J:183585
|
Capn3Gt(OST141731)Lex/Capn3Gt(OST141731)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:91206
|
Capns1tm1Pag/Capns1tm1Pag
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal neural crest cell migration
|
J:74966
|
CapopNOD/CapopNOD
(involves: C57BL/6 * NOD)
|
decreased T cell apoptosis
|
J:68151
|
Caprin1tm1Mtok/Caprin1tm1Mtok
(involves: 129S6/SvEvTac * C57BL/6)
|
increased neuron apoptosis
|
J:164650
|
Capza3repro32/Capza3repro32
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:92463
|
abnormal sperm head morphology
|
J:92463
|
asthenozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
Car5atm1Sly/Car5atm1Sly Car5btm1Sly/Y
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
oxidative stress
|
J:181790
|
Car5atm1Sly/Car5atm1Sly Car5btm1Sly/Car5btm1Sly
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
oxidative stress
|
J:181790
|
Card11em1Welu/Card11em1Welu
(involves: C57BL/6)
|
decreased B cell proliferation
|
J:292926
|
Card11em2Welu/Card11em2Welu
(involves: C57BL/6)
|
increased B cell proliferation
|
J:292926
|
Card11m1Btlr/Card11m1Btlr
(C57BL/6J-Card11m1Btlr)
|
decreased B cell proliferation
|
J:149767,
J:139069
|
decreased T cell proliferation
|
J:149767,
J:139069
|
Card11tm1Litt/Card11tm1Litt
(involves: 129P2/OlaHsd)
|
abnormal B cell proliferation
|
J:89322
|
abnormal T cell proliferation
|
J:89322
|
Card11tm1Pngr/Card11tm1Pngr
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:84036
|
Card11tm1Vmd/Card11+
(involves: 129S6/SvEvTac * C57BL/6N)
|
decreased B cell proliferation
|
J:95800
|
Card11tm1Vmd/Card11tm1Vmd
(involves: 129S6/SvEvTac * C57BL/6N)
|
decreased B cell proliferation
|
J:95800
|
decreased T cell proliferation
|
J:95800
|
Card14em9Lutzy/Card14+
(C57BL/6J-Card14em9Lutzy/J)
|
increased keratinocyte proliferation
|
J:262723
|
Card19tm1Rwen/Card19tm1Rwen Tg(IghelMD4)4Ccg/0 Tg(ML5sHEL)5Ccg/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JSfd)
|
decreased B cell proliferation
|
J:336763
|
increased B cell apoptosis
|
J:336763
|
Carm1tm1.1Mtb/Carm1tm1.1Mtb Tg(Stra8-icre)1Reb/0
(involves: 129 * C57BL/6J * FVB/NJ)
|
abnormal sperm head morphology
|
J:265753
|
abnormal sperm midpiece morphology
|
J:265753
|
absent sperm head
|
J:265753
|
asthenozoospermia
|
J:265753
|
decreased elongated spermatid number
|
J:265753
|
decreased male germ cell number
|
J:265753
|
oligozoospermia
|
J:265753
|
Carmil2bas/Carmil2bas
(involves: C3HeB/FeJ * C57BL/6)
|
decreased T cell proliferation
|
J:205441
|
Carmil2bas/Carmil2tm1a(KOMP)Mbp
(involves: C3HeB/FeJ * C57BL/6 * C57BL/6N)
|
decreased T cell proliferation
|
J:205441
|
Cars2em1Akai/Cars2+
(involves: C57BL/6N)
|
abnormal mitochondrial physiology
|
J:254717
|
Cars2em2Akai/Cars2+
(involves: C57BL/6N)
|
abnormal mitochondrial physiology
|
J:254717
|
Casktm1Sud/Casktm1.1Sud Tg(Prm-cre)58Og/0
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
increased neuron apoptosis
|
J:117978
|
Casp1tm1Flv/Casp1tm1Flv Casp4del/Casp4del
(involves: 129S2/SvPas * C57BL/6)
|
decreased thymocyte apoptosis
|
J:24258
|
impaired neutrophil chemotaxis
|
J:124226
|
Casp1tm1Sesh/Casp1tm1Sesh Casp4del/Casp4del
(involves: 129S2/SvPas * C57BL/6)
|
abnormal apoptosis
|
J:80568
|
abnormal cell migration
|
J:68644
|
cellular phenotype
|
J:22964,
J:40691
|
decreased neuron apoptosis
|
J:88212
|
decreased T cell apoptosis
|
J:40691
|
Casp1tm1Sesh/Casp1tm1Sesh Casp4del/Casp4del
(B10.Cg-Casp1tm1Sesh Casp4del H2r H2-T18b)
|
decreased apoptosis
|
J:63488
|
Casp1tm1Sesh/Casp1tm1Sesh Casp4del/Casp4del
(B6.129S2(NOD)-Casp1tm1Sesh Casp4del)
|
decreased apoptosis
|
J:243487
|
decreased macrophage apoptosis
|
J:193522
|
Casp1tm1Sesh/Casp1tm1Sesh Casp4del/Casp4del Tg(Casp4)#Gne/0
(involves: 129S2/SvPas * C57BL/6 * NOD/ShiLtJ)
|
decreased macrophage apoptosis
|
J:193522
|
Casp2tm1Vaux/Casp2tm1Vaux
(involves: 129S1/Sv * C57BL/6)
|
cellular phenotype
|
J:103480
|
Casp2tm1Yuan/Casp2tm1Yuan
(involves: 129S4/SvJae * C57BL/6J * DBA/2)
|
abnormal apoptosis
|
J:47601
|
abnormal B cell apoptosis
|
J:47601
|
abnormal female germ cell morphology
|
J:47601
|
abnormal neuron apoptosis
|
J:47601
|
abnormal oocyte morphology
|
J:47601
|
Casp3m1H/Casp3m1H
(involves: BALB/c * C3H/HeH)
|
decreased apoptosis
|
J:169366
|
Casp3tm1Dsp/Casp3tm1Dsp
(involves: 129X1/SvJ)
|
decreased neuron apoptosis
|
J:90572
|
Casp3tm1Flv/Casp3tm1Flv
(involves: 129S1/Sv * C57BL/6)
|
cellular phenotype
|
J:59875,
J:66953
|
decreased apoptosis
|
J:36821
|
Casp3tm1Flv/Casp3tm1Flv
(B6.129S1-Casp3tm1Flv)
|
abnormal apoptosis
|
J:65496
|
decreased fibroblast apoptosis
|
J:105496
|
decreased sensitivity to induced cell death
|
J:105496
|
Casp3tm1Flv/Casp3tm1Flv
(B6N.129S1-Casp3tm1Flv/J)
|
decreased keratinocyte apoptosis
|
J:189241
|
increased cardiomyocyte apoptosis
|
J:189241
|
increased cellular sensitivity to ultraviolet irradiation
|
J:189241
|
increased sensitivity to induced cell death
|
J:189241
|
Casp3tm1Flv/Casp3tm1Flv Casp7tm1Flv/Casp7+
(B6.129S-Casp3tm1Flv Casp7tm1Flv)
|
decreased fibroblast apoptosis
|
J:105496
|
decreased sensitivity to induced cell death
|
J:105496
|
decreased thymocyte apoptosis
|
J:105496
|
Casp3tm1Flv/Casp3tm1Flv Casp7tm1Flv/Casp7tm1Flv
(B6.129S-Casp3tm1Flv Casp7tm1Flv)
|
decreased fibroblast apoptosis
|
J:105496
|
decreased sensitivity to induced cell death
|
J:105496
|
decreased thymocyte apoptosis
|
J:105496
|
Casp3tm1Flv/Casp3tm1Flv Pde6brd1/Pde6brd1
(involves: 129S1/Sv * C3H/FeJ * C57BL/6J)
|
abnormal apoptosis
|
J:88367
|
Casp3tm1Flv/Casp3tm1Flv Tg(Scgb1a1-rtTA,tetO-Ifng)14Eli/0
(involves: 129S1/Sv * C57BL/6 * CBA)
|
increased apoptosis
|
J:100854
|
Casp3tm1Mak/Casp3tm1Mak Tg(TcrLCMV)327Sdz/0
(B6.Cg-Casp3tm1Mak Tg(TcrLCMV)327Sdz)
|
decreased cell proliferation
|
J:97650
|
Casp4tm1.1Vmd/Casp4tm1.1Vmd
(involves: C57BL/6)
|
decreased macrophage apoptosis
|
J:193522
|
Casp6tm1.2Xen/Casp6+
(FVB.B6NTac-Casp6tm1.2Xen)
|
decreased susceptibility to neuronal excitotoxicity
|
J:181879
|
Casp6tm1.2Xen/Casp6tm1.2Xen
(FVB.B6NTac-Casp6tm1.2Xen)
|
decreased susceptibility to neuronal excitotoxicity
|
J:181879
|
Casp6tm1Flv/Casp6tm1Flv
(Not Specified)
|
cellular phenotype
|
J:59875
|
Casp7tm1Flv/Casp7tm1Flv
(B6.129S6-Casp7tm1Flv)
|
decreased fibroblast apoptosis
|
J:105496
|
Casp8em1Hbz/Casp8em1Hbz
(involves: C57BL/6)
|
decreased apoptosis
|
J:342732
|
Casp8tm1.1Raz/Casp8tm1.1Raz Ripk3tm1Vmd/Ripk3tm1Vmd
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
decreased hepatocyte apoptosis
|
J:170814
|
decreased macrophage apoptosis
|
J:170815
|
decreased thymocyte apoptosis
|
J:170814
|
Casp8tm1Hed/Casp8tm1Hed Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:116713
|
increased apoptosis
|
J:116713
|
Casp8tm1Raz/Casp8tm1Raz Tg(Lck-cre)548Jxm/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal T cell proliferation
|
J:107455
|
decreased T cell apoptosis
|
J:82759
|
decreased T cell proliferation
|
J:82759
|
Casp8tm1Syon/Casp8tm1Syon
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:103506
|
Casp8tm1Syon/Casp8tm1Syon Tg(Myh7-BVp35-EGFP)#Ksa/?
(involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:102279
|
Casp8tm1Wll/Casp8tm1.1Yuan Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129S1/Sv * 129X1/SvJ * MF1)
|
abnormal macrophage differentiation
|
J:92722
|
Casp8tm1Yuan/Casp8tm1Yuan
(involves: 129S1/Sv * 129X1/SvJ * MF1)
|
abnormal cell death
|
J:49459
|
Casp9tm1Flv/Casp9tm1Flv
(involves: 129S1/Sv * C57BL/6)
|
abnormal apoptosis
|
J:103480,
J:66953
|
abnormal thymocyte apoptosis
|
J:49088
|
cellular phenotype
|
J:49088
|
decreased neuron apoptosis
|
J:49088,
J:90572
|
decreased T cell apoptosis
|
J:91156
|
Casp9tm1Flv/Casp9tm1Flv
(B6.129S1-Casp9tm1Flv)
|
abnormal apoptosis
|
J:65496
|
Casp9tm1Mak/Casp9tm1Mak
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1))
|
abnormal cell physiology
|
J:49087
|
abnormal respiratory electron transport chain
|
J:49087
|
abnormal splenocyte apoptosis
|
J:49087
|
abnormal thymocyte apoptosis
|
J:49087
|
decreased apoptosis
|
J:49087
|
decreased cellular sensitivity to gamma-irradiation
|
J:49087
|
decreased neuron apoptosis
|
J:49087
|
decreased sensitivity to induced cell death
|
J:49087
|
Casp12tm1Yuan/Casp12tm1Yuan
(involves: 129S4/SvJae * C57BL/6J)
|
cellular phenotype
|
J:59337
|
decreased sensitivity to induced cell death
|
J:59337
|
decreased susceptibility to neuronal excitotoxicity
|
J:59337
|
Casp12tm1Yuan/Casp12tm1Yuan Plp1jp-msd/Y
(involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/10 * BALB/c)
|
increased apoptosis
|
J:121540
|
Casp12tm1Yuan/Casp12tm1Yuan Plp1jp-rsh/Y
(involves: 129S4/SvJae * C3H * C57BL/6 * STOCK Rb(1.3)1Bnr)
|
increased apoptosis
|
J:121540
|
Casrtm1Wch/Casrtm1Wch Tg(Vil1-cre)997Gum/0
(involves: 129S4/SvJae * C57BL/6J * SJL)
|
abnormal enterocyte proliferation
|
J:179672
|
Casttm1Tcs/Casttm1Tcs
(B6.129-Casttm1Tcs)
|
increased susceptibility to neuronal excitotoxicity
|
J:109976
|
Casz1Gt(CJ0565)Wtsi/Casz1Gt(CJ0565)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:242127
|
Casz1tm1.1Flc/Casz1tm1.1Flc Isl1tm1(cre)Tmj/Isl1+
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL)
|
decreased mitotic index
|
J:221324
|
Casz1tm1.1Flc/Casz1tm1.1Flc Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL)
|
abnormal cell cycle checkpoint function
|
J:221324
|
decreased fetal cardiomyocyte proliferation
|
J:221324
|
decreased mitotic index
|
J:221324
|
Catb/Catb
(Not Specified)
|
abnormal redox activity
|
J:105024
|
Catc/Catc
(Not Specified)
|
abnormal redox activity
|
J:105024
|
Catd/Catd
(Not Specified)
|
abnormal redox activity
|
J:105024
|
Cate/Cate
(Not Specified)
|
abnormal redox activity
|
J:105024
|
Catf/Catf
(Not Specified)
|
abnormal redox activity
|
J:105024
|
Cattm1Ysh/Cattm1Ysh
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal aerobic respiration
|
J:91752
|
Catsper1tm1Clph/Catsper1tm1Clph
(involves: 129S4/SvJae * C57BL/6J)
|
asthenozoospermia
|
J:72046
|
Catsper1tm1Clph/Catsper1tm1Clph
(involves: 129S4/SvJae)
|
abnormal sperm motility
|
J:116406
|
asthenozoospermia
|
J:116406
|
Catsper2tm1Gar/Catsper2tm1Gar
(involves: 129S6/SvEvTac * C57BL/6J)
|
asthenozoospermia
|
J:86972
|
Catsper2tm1Gar/Catsper2tm1Gar
(involves: 129S6/SvEvTac)
|
abnormal sperm motility
|
J:116406
|
asthenozoospermia
|
J:116406
|
Catsper3tm1Clph/Catsper3tm1Clph
(involves: 129S4/SvJae)
|
abnormal sperm motility
|
J:116406
|
asthenozoospermia
|
J:116406
|
teratozoospermia
|
J:116406
|
Catsper3tm1Wyan/Catsper3tm1Wyan
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal sperm motility
|
J:124054
|
Catsper4tm1Clph/Catsper4tm1Clph
(involves: 129S4/SvJae)
|
abnormal sperm motility
|
J:116406
|
asthenozoospermia
|
J:116406
|
teratozoospermia
|
J:116406
|
Catsper4tm1Wyan/Catsper4tm1Wyan
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal sperm motility
|
J:124054
|
Catsperdtm1.1Clph/Catsperdtm1.1Clph
(involves: 129S4/SvJae * C57BL/6)
|
abnormal germ cell morphology
|
J:182472
|
decreased hyperactivated sperm motility
|
J:182472
|
oligozoospermia
|
J:182472
|
teratozoospermia
|
J:182472
|
Catsperztm1(KOMP)Mbp/Catsperztm1(KOMP)Mbp
(C57BL/6N-Catsperztm1(KOMP)Mbp)
|
abnormal sperm migration in female genital tract
|
J:239219
|
decreased hyperactivated sperm motility
|
J:239219
|
Catsperztm1(KOMP)Mbp/Catsperztm1(KOMP)Mbp Efcab9em1Chng/Efcab9em1Chng
(involves: C57BL/6 * C57BL/6N)
|
decreased hyperactivated sperm motility
|
J:276402
|
Cav1tm1Krc/Cav1tm1Krc
(involves: 129S4/SvJae * Black Swiss)
|
absent caveolae
|
J:78603
|
Cav1tm1Kur/Cav1tm1Kur
(involves: 129X1/SvJ * C57BL/6)
|
absent caveolae
|
J:71760
|
cellular phenotype
|
J:71760
|
decreased hepatocyte proliferation
|
J:112452
|
increased lung endothelial cell proliferation
|
J:71760
|
Cav1tm1Mls/Cav1tm1Mls
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal vesicle-mediated transport
|
J:73489
|
absent caveolae
|
J:75192,
J:75193,
J:73489
|
Cav1tm1Mls/Cav1tm1Mls
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal actin cytoskeleton morphology
|
J:134719
|
abnormal cell morphology
|
J:134719
|
abnormal cellular cholesterol metabolism
|
J:116292
|
abnormal fibroblast chemotaxis
|
J:134719
|
abnormal microtubule organizing center morphology
|
J:134719
|
absent caveolae
|
J:115492,
J:128103,
J:114334
|
decreased fibroblast chemotaxis
|
J:134719
|
Cav1tm1Mls/Cav1tm1Mls
(B6.Cg-Cav1tm1Mls)
|
absent caveolae
|
J:205741
|
Cav1tm1Mls/Cav1tm1Mls
(B6.Cg-Cav1tm1Mls/J)
|
absent caveolae
|
J:143600
|
Cav1tm1Mls/Cav1tm1Mls
(Not Specified)
|
abnormal cell cytoskeleton morphology
|
J:168335
|
Cav1tm1Mls/Cav1tm1Mls
(FVB.Cg-Cav1tm1Mls)
|
abnormal cellular respiration
|
J:182288
|
abnormal respiratory electron transport chain
|
J:182288
|
Cav1tm1Mls/Cav1tm1Mls Cav3tm1Mls/Cav3tm1Mls
(involves: 129/Sv * C57BL/6J * SJL)
|
absent caveolae
|
J:77372
|
cardiac interstitial fibrosis
|
J:77372
|
Cav1tm1Mls/Cav1tm1Mls Cdkn2atm1Rdp/Cdkn2atm1Rdp
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal cell cycle
|
J:90334
|
increased fibroblast proliferation
|
J:90334
|
Cav2tm1Mls/Cav2tm1Mls
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal basement membrane morphology
|
J:75490
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:117199
|
cellular phenotype
|
J:117199,
J:75490
|
Cav3tm1Mls/Cav3tm1Mls
(involves: 129/Sv * C57BL/6J * SJL)
|
absent caveolae
|
J:79453
|
Cavin1tm1Pfp/Cavin1tm1Pfp
(involves: 129S6/SvEvTac * C57BL/6)
|
absent caveolae
|
J:143425,
J:205741
|
Cavin1tm1Pfp/Cavin1tm1Pfp
(B6.129S6-Cavin1tm1Pfp/J)
|
absent caveolae
|
J:217258,
J:217273
|
Cavin2tm1(KOMP)Vlcg/Cavin2tm1(KOMP)Vlcg
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal plasma membrane morphology
|
J:205741
|
Cavin3tm1(KOMP)Vlcg/Cavin3tm1(KOMP)Vlcg
(involves: C57BL/6 * C57BL/6NTac)
|
cellular phenotype
|
J:205741
|
Cavin3tm1(KOMP)Vlcg/Cavin3tm1(KOMP)Vlcg Cavin2tm1(KOMP)Vlcg/Cavin2tm1(KOMP)Vlcg
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal plasma membrane morphology
|
J:205741
|
Cavin3tm1Pemi/Cavin3tm1Pemi
(B6.129S4-Cavin3tm1Pemi)
|
abnormal cellular respiration
|
J:202374
|
Cbfa2t2em1Dare/Cbfa2t2em1Dare
(C57BL/6-Cbfa2t2em1Dare)
|
abnormal epigenetic regulation of gene expression
|
J:233954
|
abnormal primordial germ cell morphology
|
J:233954
|
asthenozoospermia
|
J:233954
|
decreased male germ cell number
|
J:233954
|
decreased primordial germ cell number
|
J:233954
|
oligozoospermia
|
J:233954
|
Cbfa2t2tm1Swh/Cbfa2t2tm1Swh
(either: B6.129S6-Cbfa2t2tm1Swh or (involves: 129S6/SvEvTac * C57BL/6))
|
abnormal intestinal goblet cell morphology
|
J:102172
|
Cbfbtm1Lhc/Cbfbtm1Lhc Tg(Mx1-cre)1Cgn/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal megakaryocyte differentiation
|
J:105040
|
Cbfbtm1Ppl/Cbfb+
(either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6))
|
increased apoptosis
|
J:36594
|
Cbfbtm1Spe/Cbfbtm1Spe
(either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6))
|
increased apoptosis
|
J:36593
|
Cbfbtm1Spe/Cbfbtm1Spe Tg(Tek-GFP/Cbfb)1Spe/0
(either: (involves: 129S4/SvJae * BALB/c * CD-1) or (involves: 129S4/SvJae * C57BL/6 * CD-1))
|
abnormal osteoblast differentiation
|
J:80670
|
Cbfbtm1Spe/Cbfbtm1Spe Tg(Tek-GFP/Cbfb)2Spe/0
(either: (involves: 129S4/SvJae * BALB/c * CD-1 * Swiss Webster) or (involves: 129S4/SvJae * C57BL/6 * CD-1 * Swiss Webster))
|
abnormal osteoblast differentiation
|
J:80670
|
Cbfbtm1Tok/Cbfbtm1Tok Tg(Gata1-Cbfb)1Tok/0
(involves: 129P2/OlaHsd * C57BL/6J)
|
arrested osteoblast differentiation
|
J:80668
|
Cbfbtm5Ppl/Cbfb+
(Not Specified)
|
abnormal mononuclear cell differentiation
|
J:193140
|
Cbltm1Ddlb/Cbltm1Ddlb
(involves: 129S1/Sv * C57BL/6)
|
increased mitochondrial size
|
J:94416
|
increased skeletal muscle cell glucose uptake
|
J:94416
|
Cbltm2Hua/Cbltm2Hua Cblbtm1Hua/Cblbtm1Hua Tg(Lck-cre)I57Jxm/0
(involves: 129P2/OlaHsd * C57BL/6 * ICR)
|
increased T cell proliferation
|
J:80427
|
Cblbtm1Hua/Cblbtm1Hua
(Not Specified)
|
increased T cell proliferation
|
J:89761
|
Cblbtm1Hua/Cblbtm1Hua
(B6.129P2-Cblbtm1Hua)
|
increased T cell proliferation
|
J:94685
|
Cblbtm1Hua/Cblbtm1Hua Ubash3btm1Jni/Ubash3btm1Jni Ubash3atm1Jni/Ubash3atm1Jni
(Not Specified)
|
increased T cell proliferation
|
J:89761
|
Cblbtm1Pngr/Cblbtm1Pngr
(B6.129P2-Cblbtm1Pngr)
|
increased T cell proliferation
|
J:141390
|
Cbliftm1a(KOMP)Wtsi/Cbliftm1a(KOMP)Wtsi
(C57BL/6N-Cbliftm1a(KOMP)Wtsi)
|
maternal effect
|
J:236022
|
CbllTg(Alb-KL)7-2Mhos/CbllTg(Alb-KL)7-2Mhos
(involves: C57BL/6)
|
abnormal Purkinje cell differentiation
|
J:100997
|
Cbstm1Unc/Cbstm1Unc
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal keratinocyte differentiation
|
J:105571
|
increased hepatocyte apoptosis
|
J:101303
|
oxidative stress
|
J:101303
|
Cbx2tm1Cim/Cbx2tm1Cim
(involves: 129P2/OlaHsd * BALB/c)
|
decreased fibroblast proliferation
|
J:38487
|
decreased splenocyte proliferation
|
J:38487
|
Cbx3tm1Pbs/Cbx3tm1Pbs
(involves: 129)
|
oligozoospermia
|
J:186901
|
Cbx7tm1Afus/Cbx7tm1Afus
(involves: C57BL/6J)
|
abnormal cell cycle
|
J:184383
|
abnormal cell death
|
J:184383
|
increased fibroblast proliferation
|
J:184383
|
Cbx8tm1.1Hko/Cbx8tm1.1Hko
(involves: 129 * C57BL/6)
|
abnormal cell physiology
|
J:178955
|
Cbx8tm1Hko/Cbx8tm1Hko Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: 129 * C57BL/6 * C57BL/6NTac)
|
abnormal cell physiology
|
J:178955
|
Cby1tm1Ktkm/Cby1tm1Ktkm
(Not Specified)
|
abnormal fat cell differentiation
|
J:122334
|
Cby1tm1Ktkm/Cby1tm1Ktkm
(B6.129-Cby1tm1Ktkm)
|
abnormal respiratory motile cilium morphology
|
J:166685
|
decreased respiratory motile cilia number
|
J:166685,
J:147413
|
Cc2d1atm1.2Thkn/Cc2d1atm1.2Thkn
(involves: 129S4/SvJae * BALB/cJ * C57BL/6 * SJL)
|
abnormal cell morphology
|
J:236761
|
Cc2d1atm1Bisu/Cc2d1atm1Bisu
(Not Specified)
|
increased cellular sensitivity to hydrogen peroxide
|
J:184920
|
Cc2d2aGt(AA0274)Wtsi/Cc2d2aGt(AA0274)Wtsi
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:176174
|
Cc2d2atm1Asw/Cc2d2atm1Asw
(Not Specified)
|
abnormal kinocilium morphology
|
J:226310
|
abnormal nonmotile primary cilium morphology
|
J:226310
|
abnormal primary cilium morphology
|
J:226310
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:226310
|
abnormal vesicle-mediated transport
|
J:226310
|
decreased embryonic cilium number
|
J:226310
|
decreased embryonic neuroepithelium primary cilium number
|
J:226310
|
decreased respiratory motile cilia number
|
J:226310
|
Ccbe1tm1Mlkn/Ccbe1tm1Mlkn
(either: B6.129-Ccbe1tm1Mlkn or (involves: 129 * C57BL/6))
|
increased apoptosis
|
J:196696
|
Ccdc6tm1Afus/Ccdc6tm1Afus
(involves: 129 * C57BL/6J)
|
abnormal cell cycle
|
J:301625
|
decreased fibroblast proliferation
|
J:301625
|
increased cellular sensitivity to hydrogen peroxide
|
J:301625
|
increased fibroblast apoptosis
|
J:301625
|
Ccdc8tm1.2Yxi/Ccdc8tm1.2Yxi
(B6.129P2(Cg)-Ccdc8tm1.2Yxi)
|
cellular phenotype
|
J:303998
|
decreased fibroblast cell migration
|
J:303998
|
Ccdc28aem1Lwa/Ccdc28aem1Lwa
(involves: C57BL/6N * DBA/2)
|
abnormal acroplaxome morphology
|
J:350809
|
abnormal acrosome morphology
|
J:350809
|
abnormal sperm head morphology
|
J:350809
|
asthenozoospermia
|
J:350809
|
decreased sperm progressive motility
|
J:350809
|
detached acrosome
|
J:350809
|
small sperm head
|
J:350809
|
Ccdc28bem1Jlba/Ccdc28bem1Jlba
(C57BL/6J-Ccdc28bem1Jlba)
|
abnormal cilium morphology
|
J:325766
|
Ccdc34em1Fzg/Ccdc34em1Fzg
(C57BL/6-Ccdc34em1Fzg)
|
abnormal outer dense fiber morphology
|
J:333018
|
abnormal sperm axoneme morphology
|
J:333018
|
asthenozoospermia
|
J:333018
|
increased male germ cell apoptosis
|
J:333018
|
oligozoospermia
|
J:333018
|
teratozoospermia
|
J:333018
|
Ccdc38em1Cya/Ccdc38em1Cya
(C57BL/6J-Ccdc38em1Cya/Cya)
|
abnormal outer dense fiber morphology
|
J:325559
|
abnormal sperm axoneme morphology
|
J:325559
|
abnormal sperm fibrous sheath morphology
|
J:325559
|
abnormal sperm flagellum morphology
|
J:325559
|
abnormal sperm head morphology
|
J:325559
|
abnormal sperm mitochondrial sheath morphology
|
J:325559
|
abnormal sperm nucleus morphology
|
J:325559
|
abnormal spermatid morphology
|
J:325559
|
absent sperm flagellum
|
J:325559
|
asthenozoospermia
|
J:325559
|
coiled sperm flagellum
|
J:325559
|
ectopic manchette
|
J:325559
|
elongated manchette
|
J:325559
|
oligozoospermia
|
J:325559
|
short sperm flagellum
|
J:325559
|
teratozoospermia
|
J:325559
|
thin sperm flagellum
|
J:325559
|
Ccdc39b2b1304Clo/Ccdc39b2b1304Clo
(C57BL/6J-Ccdc39b2b1304Clo)
|
immotile respiratory cilia
|
J:175213
|
Ccdc39b2b1735Clo/Ccdc39b2b1735Clo
(C57BL/6J-Ccdc39b2b1735Clo)
|
immotile respiratory cilia
|
J:175213
|
Ccdc39prh/Ccdc39prh
(involves: A/J * FVB/N)
|
abnormal brain ependyma motile cilium morphology
|
J:253968
|
abnormal brain ependyma motile cilium physiology
|
J:253968
|
Ccdc40lnks/Ccdc40lnks
(involves: C3H/HeJ * C57BL/6J)
|
abnormal motile primary cilium morphology
|
J:168691
|
Ccdc42tm1(KOMP)Vlcg/Ccdc42tm1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
abnormal acrosome morphology
|
J:231668
|
abnormal sperm axoneme morphology
|
J:231668
|
abnormal sperm connecting piece morphology
|
J:231668
|
abnormal sperm flagellum morphology
|
J:231668
|
abnormal sperm head morphology
|
J:231668
|
abnormal sperm nucleus morphology
|
J:231668
|
abnormal spermatid morphology
|
J:231668
|
absent sperm flagellum
|
J:231668
|
azoospermia
|
J:231668
|
detached acrosome
|
J:231668
|
Ccdc47tm1Hta/Ccdc47tm1Hta
(involves: C57BL/6J)
|
abnormal cell physiology
|
J:124441
|
increased fibroblast apoptosis
|
J:124441
|
Ccdc51tm1.1Geno/Ccdc51tm1.1Geno
(involves: C57BL/6N)
|
abnormal mitochondrial physiology
|
J:279978
|
Ccdc62em1Jxia/Ccdc62em1Jxia
(C57BL/6-Ccdc62em1Jxia)
|
abnormal sperm head morphology
|
J:244081
|
abnormal sperm midpiece morphology
|
J:244081
|
asthenozoospermia
|
J:244081
|
teratozoospermia
|
J:244081
|
Ccdc62repro29/Ccdc62repro29
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal sperm head morphology
|
J:244081
|
abnormal sperm midpiece morphology
|
J:244081
|
absent acrosome
|
J:244081
|
asthenozoospermia
|
J:244081,
J:92463
|
oligozoospermia
|
J:92463
|
teratozoospermia
|
J:244081,
J:92463
|
Ccdc63em1Osb/Ccdc63em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm flagellum morphology
|
J:231237
|
abnormal sperm head morphology
|
J:231237
|
asthenozoospermia
|
J:231237
|
short sperm flagellum
|
J:231237
|
Ccdc80tm1Ppal/Ccdc80+
(Not Specified)
|
increased fibroblast proliferation
|
J:217742
|
Ccdc80tm1Ppal/Ccdc80tm1Ppal
(Not Specified)
|
decreased fibroblast apoptosis
|
J:217742
|
increased fibroblast proliferation
|
J:217742
|
Ccdc86tm1Hfuj/Ccdc86+
(involves: C57BL/6NTac)
|
decreased T cell apoptosis
|
J:151722
|
Ccdc87tm1(KOMP)Vlcg/Ccdc87tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal acrosome assembly
|
J:265624
|
abnormal sperm head morphology
|
J:265624
|
abnormal sperm motility
|
J:265624
|
abnormal sperm nucleus morphology
|
J:265624
|
Ccdc88atm1Mat/Ccdc88atm1Mat
(Not Specified)
|
abnormal neuron differentiation
|
J:173379
|
abnormal neuronal precursor cell migration
|
J:173379
|
Ccdc88atm3.1Mat/Ccdc88atm3.1Mat
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal neuronal precursor cell migration
|
J:173379
|
Ccdc88bm1Pgrs/Ccdc88bm1Pgrs
(involves: C57BL/6J * C57BL/10J)
|
decreased T cell proliferation
|
J:230618
|
Ccdc88ctm1(KOMP)Mbp/Ccdc88ctm1(KOMP)Mbp
(C57BL/6N-Ccdc88ctm1(KOMP)Mbp)
|
abnormal brain ependyma motile cilium location or orientation
|
J:292096
|
Ccdc92tm1a(KOMP)Mbp/Ccdc92tm1a(KOMP)Mbp
(C57BL/6N-Ccdc92tm1a(KOMP)Mbp)
|
abnormal fat cell differentiation
|
J:332421
|
Ccdc93em1(IMPC)J/Ccdc93em1(IMPC)J
(C57BL/6NJ-Ccdc93em1(IMPC)J/Mmjax)
|
increased embryonic tissue cell apoptosis
|
J:279207
|
Ccdc134tm1.2Jhua/Ccdc134tm1.2Jhua
(involves: C57BL/6NTac)
|
decreased hepatocyte proliferation
|
J:256995
|
Ccdc136em1Smoc/Ccdc136em1Smoc
(involves: C57BL/6J)
|
abnormal sperm nucleus morphology
|
J:237643
|
asthenozoospermia
|
J:237643
|
decreased sperm progressive motility
|
J:237643
|
globozoospermia
|
J:237643
|
Ccdc141tm1.1Ygi/Ccdc141tm1.1Ygi
(B6N(Cg)-Ccdc141tm1.1Ygi)
|
abnormal neuronal migration
|
J:238090
|
Ccdc146em1Cya/Ccdc146em1Cya
(Not Specified)
|
abnormal manchette morphology
|
J:344445
|
abnormal manchette perinuclear ring morphology
|
J:344445
|
abnormal outer dense fiber morphology
|
J:344445
|
abnormal sperm axoneme morphology
|
J:344445
|
abnormal sperm flagellum morphology
|
J:344445
|
abnormal sperm head morphology
|
J:344445
|
absent sperm flagellum
|
J:344445
|
coiled sperm flagellum
|
J:344445
|
elongated manchette
|
J:344445
|
immotile sperm
|
J:344445
|
oligozoospermia
|
J:344445
|
short sperm flagellum
|
J:344445
|
teratozoospermia
|
J:344445
|
Ccdc157em1Ymxi/Ccdc157+
(C57BL/6-Ccdc157em1Ymxi)
|
abnormal sperm head morphology
|
J:346468
|
asthenozoospermia
|
J:346468
|
Ccdc157em1Ymxi/Ccdc157em1Ymxi
(C57BL/6-Ccdc157em1Ymxi)
|
abnormal acroplaxome morphology
|
J:346468
|
abnormal acrosome assembly
|
J:346468
|
abnormal acrosome morphology
|
J:346468
|
abnormal sperm head morphology
|
J:346468
|
abnormal sperm nucleus morphology
|
J:346468
|
absent sperm head
|
J:346468
|
asthenozoospermia
|
J:346468
|
detached acrosome
|
J:346468
|
oligozoospermia
|
J:346468
|
Ccdc159em1Yingz/Ccdc159em1Yingz
(involves: C57BL/6NCr)
|
abnormal acrosome morphology
|
J:351297
|
abnormal sperm axoneme morphology
|
J:351297
|
abnormal sperm connecting piece morphology
|
J:351297
|
abnormal sperm flagellum morphology
|
J:351297
|
abnormal sperm mitochondrial sheath morphology
|
J:351297
|
abnormal spermatid morphology
|
J:351297
|
absent sperm fibrous sheath
|
J:351297
|
detached sperm flagellum
|
J:351297
|
disorganized sperm mitochondrial sheath
|
J:351297
|
increased apoptosis
|
J:351297
|
increased elongated spermatid number
|
J:351297
|
increased round spermatid number
|
J:351297
|
increased spermatid number
|
J:351297
|
Ccdc181em1Qsh/Ccdc181em1Qsh
(C57BL/6J-Ccdc181em1Qsh)
|
abnormal acroplaxome morphology
|
J:359010
|
abnormal acrosome morphology
|
J:359010
|
abnormal sperm axoneme morphology
|
J:359010
|
abnormal sperm flagellum morphology
|
J:359010
|
abnormal sperm head morphology
|
J:359010
|
absent sperm flagellum
|
J:359010
|
asthenozoospermia
|
J:359010
|
coiled sperm flagellum
|
J:359010
|
detached acrosome
|
J:359010
|
elongated manchette
|
J:359010
|
increased male germ cell apoptosis
|
J:359010
|
kinked sperm flagellum
|
J:359010
|
oligozoospermia
|
J:359010
|
short sperm flagellum
|
J:359010
|
Ccdc183em1Osb/Ccdc183em1Osb
(involves: C57BL/6 * DBA)
|
abnormal manchette morphology
|
J:342837
|
abnormal outer dense fiber morphology
|
J:342837
|
abnormal sperm axoneme morphology
|
J:342837
|
abnormal sperm fibrous sheath morphology
|
J:342837
|
abnormal sperm flagellum morphology
|
J:342837
|
abnormal sperm head morphology
|
J:342837
|
abnormal sperm mitochondrial sheath morphology
|
J:342837
|
abnormal sperm principal piece morphology
|
J:342837
|
absent sperm fibrous sheath
|
J:342837
|
decreased sperm progressive motility
|
J:342837
|
immotile sperm
|
J:342837
|
oligozoospermia
|
J:342837
|
teratozoospermia
|
J:342837
|
thick sperm flagellum
|
J:342837
|
Ccdc188em1Osb/Ccdc188em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm connecting piece morphology
|
J:361702
|
abnormal sperm head morphology
|
J:361702
|
abnormal sperm midpiece morphology
|
J:361702
|
absent sperm head
|
J:361702
|
absent sperm mitochondrial sheath
|
J:361702
|
asthenozoospermia
|
J:361702
|
detached sperm flagellum
|
J:361702
|
short sperm flagellum
|
J:361702
|
Ccinem2Gpt/Ccinem2Gpt
(C57BL/6JGpt-Ccinem2Gpt/Gpt)
|
abnormal acrosome morphology
|
J:326789
|
abnormal sperm head morphology
|
J:326789
|
asthenozoospermia
|
J:326789
|
increased male germ cell apoptosis
|
J:326789
|
oligozoospermia
|
J:326789
|
Cckartm1Kpn/Cckartm1Kpn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal neuronal migration
|
J:96891
|
Ccl2tm1.1Pame/Ccl2tm1.1Pame Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
abnormal leukocyte migration
|
J:171379
|
Ccl2tm1.1Pame/Ccl2tm1.1Pame Tg(Tek-cre)12Flv/0
(involves: C3H * C57BL/6)
|
abnormal leukocyte migration
|
J:171379
|
Ccl2tm1.1Tyos/Ccl2tm1.1Tyos
(involves: 129S1/Sv * C57BL/6)
|
impaired macrophage chemotaxis
|
J:151874
|
Ccl2tm1.1Tyos/Ccl2tm1.1Tyos
(involves: 129S1/Sv)
|
abnormal dendritic cell chemotaxis
|
J:199611
|
Ccl2tm1Lex/Ccl2tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
impaired macrophage chemotaxis
|
J:191510
|
Ccl2tm1Rol/Ccl2+ Mpztm1Msch/Mpz+
(involves: 129S4/SvJae * 129S7/SvEvBrd)
|
abnormal macrophage derived foam cell morphology
|
J:133028
|
Ccl2tm1Rol/Ccl2tm1Rol
(involves: 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
impaired macrophage chemotaxis
|
J:45920
|
Ccl2tm1Rol/Ccl2tm1Rol
(involves: 129S4/SvJae * C57BL/6)
|
abnormal macrophage chemotaxis
|
J:116878
|
impaired macrophage chemotaxis
|
J:108533
|
Ccl2tm1Rol/Ccl2tm1Rol
(involves: 129S4/SvJae)
|
impaired macrophage chemotaxis
|
J:147697
|
Ccl2tm1Rol/Ccl2tm1Rol
(B6.129S4-Ccl2tm1Rol)
|
abnormal macrophage chemotaxis
|
J:109290
|
impaired macrophage chemotaxis
|
J:151874,
J:68145,
J:118606
|
Ccl2tm1Rol/Ccl2tm1Rol
(B6.129S4-Ccl2tm1Rol/J)
|
decreased susceptibility to neuronal excitotoxicity
|
J:141739
|
Ccl2tm1Rol/Ccl2tm1Rol Tg(Ccr2-EGFP)8Pame/0
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal leukocyte migration
|
J:171379
|
Ccl3tm1Unc/Ccl3tm1Unc Hexbtm1Rlp/Hexbtm1Rlp
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
cellular phenotype
|
J:90687
|
Ccl5tm1Hso/Ccl5tm1Hso
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:75842
|
Ccl17tm2.1(cre)Ifo/Ccl17+ Hif1atm3Rsjo/Hif1atm3Rsjo
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:187773
|
abnormal leukocyte migration
|
J:187773
|
Ccl27aem1Nax/Ccl27aem1Nax Ccl27alem1Nax/Ccl27alem1Nax Ccl27bem1Nax/Ccl27bem1Nax
(involves: C57BL/6)
|
impaired leukocyte migration
|
J:330550
|
Ccl27aem1Nax/Ccl27aem1Nax Ccl27alem1Nax/Ccl27alem1Nax Ccl27bem1Nax/Ccl27bem1Nax Ccr10tm1.1Nax/Ccr10+
(involves: C57BL/6)
|
impaired leukocyte migration
|
J:330550
|
Ccl28tm1Takna/Ccl28tm1Takna
(C57BL/6J-Ccl28tm1Takna)
|
abnormal cell migration
|
J:256896
|
Ccm2Gt(RRG051)Byg/Ccm2+
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:101748
|
Ccm2ltm1Mlkn/Ccm2ltm1Mlkn Heg1tm1Mlkn/Heg1tm1Mlkn
(involves: 129 * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:187714
|
Ccn1tm1Lfl/Ccn1tm1Lfl
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal apoptosis
|
J:80618
|
Ccn1tm2Lfl/Ccn1tm2Lfl
(involves: 129S4/SvJae * C57BL/6)
|
decreased apoptosis
|
J:119829
|
Ccn1tm3.1Lfl/Ccn1tm3.1Lfl Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S4/SvJae * C57BL/6 * DBA)
|
abnormal cellular replicative senescence
|
J:204032
|
Ccn2tm1Kml/Ccn2tm1Kml
(involves: 129X1/SvJ * BALB/cJ)
|
decreased mesenchymal cell proliferation involved in lung development
|
J:130165
|
Ccn3tm1.1Ecan/Ccn3tm1.1Ecan
(B6.Cg-Ccn3tm1.1Ecan)
|
abnormal osteoblast physiology
|
J:158478
|
abnormal osteoclast differentiation
|
J:158478
|
Ccn3tm1Hko/Ccn3tm1Hko
(B6.129-Ccn3tm1Hko)
|
increased vascular smooth muscle cell proliferation
|
J:172144
|
Ccna1tm1Coll/Ccna1+
(either: 129S/SvEv or (involves: 129S/SvEv * MF1))
|
oligozoospermia
|
J:89030
|
Ccna1tm1Coll/Ccna1tm1Coll
(involves: 129S/SvEv * MF1)
|
multinucleated giant male germ cells
|
J:89030
|
Ccna1tm1Djw/Ccna1tm1Djw
(involves: 129S7/SvEvBrd)
|
arrest of male meiosis
|
J:51290
|
increased male germ cell apoptosis
|
J:51290
|
multinucleated giant male germ cells
|
J:51290
|
Ccna1tm1Djw/Ccna1tm1Djw Ccna2tm1.1Pisc/Ccna2tm1.1Pisc
(involves: 129S7/SvEvBrd)
|
abnormal cell cycle
|
J:155178
|
decreased cell proliferation
|
J:155178
|
Ccna1tm1Djw/Ccna1tm1Djw Ccna2tm1.1Pisc/Ccna2tm1.2Pisc
(involves: 129S4/SvJaeSor * 129S7/SvEvBrd)
|
decreased cell proliferation
|
J:155178
|
Ccna2tm1.1Pisc/Ccna2tm1.1Pisc
(Not Specified)
|
abnormal cell cycle
|
J:155178
|
Ccnb1ip1mei4/Ccnb1ip1mei4
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal female meiosis
|
J:125220
|
abnormal meiosis
|
J:86161,
J:125220
|
abnormal oocyte morphology
|
J:125220
|
abnormal spermatocyte morphology
|
J:125220
|
absent chiasmata formation
|
J:125220
|
arrest of male meiosis
|
J:125220
|
azoospermia
|
J:125220
|
decreased oocyte number
|
J:86161
|
Ccnb3em1Sky/Ccnb3em1Sky
(involves: C57BL/6J * CBA/J)
|
abnormal female meiosis
|
J:273304
|
abnormal polar body morphology
|
J:273304
|
Ccnctm1.2Pisc/Ccnctm1.2Pisc
(Not Specified)
|
abnormal cell cycle
|
J:217695
|
Ccnd1tm1Dsn/Ccnd1tm1Dsn
(involves: 129P2/OlaHsd * C57BL/6J)
|
cellular phenotype
|
J:29258
|
Ccnd2tm1Wbg/Ccnd2tm1Wbg
(involves: 129S2/SvPas)
|
oligozoospermia
|
J:37092
|
Ccnd3tm1.1(Ccnd2)Iaai/Ccnd3tm1.1(Ccnd2)Iaai
(involves: 129S6/SvEvTac)
|
decreased B cell proliferation
|
J:192031
|
decreased T cell proliferation
|
J:192031
|
Ccnd3tm1Pisc/Ccnd3tm1Pisc
(Not Specified)
|
decreased B cell proliferation
|
J:192031
|
decreased T cell proliferation
|
J:88120,
J:192031
|
Ccnd3tm1Pisc/Ccnd3tm1Pisc Cdkn1btm1Mlf/Cdkn1btm1Mlf
(involves: 129S4/SvJaeSor)
|
decreased T cell proliferation
|
J:192031
|
Ccnd3tm1Pisc/Ccnd3tm1Pisc Rag2tm1Fwa/Rag2tm1Fwa
(involves: 129S/SvEv)
|
increased T cell proliferation
|
J:88120
|
Ccnd3tm1Pisc/Ccnd3tm1Pisc Rb1tm2Brn/Rb1tm2Brn Tg(Mx1-cre)1Cgn/0
(involves: 129 * C57BL/6 * CBA)
|
decreased T cell proliferation
|
J:192031
|
Ccndbp1tm1Riet/Ccndbp1tm1Riet
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased hepatocyte proliferation
|
J:121623
|
Ccne1tm1Clur/Ccne1tm1Clur
(involves: 129S4/SvJae)
|
increased mammary gland epithelial cell proliferation
|
J:136692
|
Ccne1tm1Jro/? Cdkn1atm1Led/Cdkn1atm1Led
(either: (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J) or (involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * C57BL/6J))
|
abnormal cell morphology
|
J:99695
|
chromosome breakage
|
J:99695
|
decreased fibroblast proliferation
|
J:99695
|
Ccne1tm1Jro/? Krastm3Tyj/?
(either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6))
|
chromosome breakage
|
J:99695
|
Ccne1tm1Jro/? Trp53tm1Tyj/Trp53tm1Tyj
(either: (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6J) or (involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * C57BL/6J))
|
increased fibroblast proliferation
|
J:99695
|
Ccne1tm1Jro/Ccne1tm1Jro
(either: 129-Ccne1tm1Jro or B6.129-Ccne1tm1Jro)
|
abnormal cell physiology
|
J:99695
|
increased splenocyte proliferation
|
J:99695
|
Ccne1tm1Jro/Ccne1tm1Jro
(involves: 129/Sv * 129S4/SvJaeSor)
|
increased mammary gland epithelial cell proliferation
|
J:136692
|
Ccne2tm1Boa/Ccne2tm1Boa
(involves: 129/Sv * C57BL/6)
|
oligozoospermia
|
J:85497
|
Ccne2tm1Pisc/Ccne2tm1Pisc
(involves: 129S2/SvPas)
|
abnormal male meiosis
|
J:85224
|
multinucleated giant male germ cells
|
J:85224
|
oligozoospermia
|
J:85224
|
Ccnftm1.1Sje/Ccnftm1.1Sje
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle
|
J:89060
|
decreased cell proliferation
|
J:89060
|
Ccng1tm1Noj/Ccng1tm1Noj
(involves: 129S2/SvPas * C57BL/6J)
|
increased cellular sensitivity to gamma-irradiation
|
J:106744
|
Ccnitm1Jro/Ccnitm1Jro
(involves: 129S4/SvJaeSor)
|
increased podocyte apoptosis
|
J:115356
|
increased renal glomerulus apoptosis
|
J:115356
|
Ccnytm1.1Smoc/Ccnytm1.1Smoc
(involves: C57BL/6)
|
abnormal fat cell differentiation
|
J:224589
|
Ccnyl1tm1a(EUCOMM)Wtsi/Ccnyl1tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal sperm annulus morphology
|
J:224586
|
absent sperm mitochondrial sheath
|
J:224586
|
asthenozoospermia
|
J:224586
|
decreased sperm progressive motility
|
J:224586
|
teratozoospermia
|
J:224586
|
Ccp110tm1.2Asw/Ccp110+
(involves: C57BL/6J)
|
abnormal cell cycle
|
J:232855
|
Ccp110tm1.2Asw/Ccp110tm1.2Asw
(involves: C57BL/6J)
|
abnormal brain ependyma motile cilium morphology
|
J:232855
|
abnormal cell cycle
|
J:232855
|
abnormal cell morphology
|
J:232855
|
abnormal cilium morphology
|
J:232855
|
abnormal kidney epithelial cell primary cilium morphology
|
J:232855
|
abnormal mitotic spindle morphology
|
J:232855
|
aneuploidy
|
J:232855
|
decreased embryonic neuroepithelium primary cilium number
|
J:232855
|
increased mitotic index
|
J:232855
|
polyploidy
|
J:232855
|
spontaneous chromosome breakage
|
J:232855
|
Ccpg1tm1a(EUCOMM)Hmgu/Ccpg1tm1a(EUCOMM)Hmgu
(C57BL/6N-Ccpg1tm1a(EUCOMM)Hmgu)
|
abnormal endoplasmic reticulum morphology
|
J:256708
|
abnormal reticulophagy
|
J:256708
|
increased endoplasmic reticulum stress
|
J:256708
|
Ccr1tm1Gao/Ccr1tm1Gao
(B6.129S4-Ccr1tm1Gao)
|
abnormal cellular extravasation
|
J:104744
|
abnormal leukocyte adhesion
|
J:104744
|
Ccr2tm1.1Dnc/Ccr2tm1.1Dnc
(Not Specified)
|
abnormal dendritic cell chemotaxis
|
J:223508
|
Ccr2tm1Blck/Ccr2tm1Blck
(B6.129P2-Ccr2tm1Blck)
|
abnormal cellular extravasation
|
J:104744
|
abnormal leukocyte adhesion
|
J:104744
|
Ccr2tm1Brv/Ccr2tm1Brv
(involves: 129S1/Sv * ICR)
|
impaired macrophage chemotaxis
|
J:111517
|
Ccr2tm1Ifc/Ccr2+
(involves: 129S4/SvJae * C57BL/6)
|
impaired macrophage chemotaxis
|
J:121703
|
Ccr2tm1Ifc/Ccr2tm1Ifc
(B6.129S4-Ccr2tm1Ifc/J)
|
abnormal leukocyte migration
|
J:106738
|
abnormal osteoclast differentiation
|
J:149360
|
Ccr2tm1Ifc/Ccr2tm1Ifc
(involves: 129S4/SvJae * C57BL/6)
|
abnormal macrophage chemotaxis
|
J:44345
|
decreased splenocyte proliferation
|
J:75838
|
decreased T cell proliferation
|
J:75838
|
impaired macrophage chemotaxis
|
J:81363,
J:44345,
J:121703
|
increased hepatocyte apoptosis
|
J:61542
|
Ccr2tm1Ifc/Ccr2tm1Ifc
(B6.129S4-Ccr2tm1Ifc)
|
impaired leukocyte tethering or rolling
|
J:154558
|
Ccr2tm1Mae/Ccr2tm1Mae
(involves: 129P2/OlaHsd)
|
abnormal leukocyte migration
|
J:171379
|
impaired macrophage chemotaxis
|
J:191510,
J:151874
|
Ccr2tm1Mae/Ccr2tm1Mae
(involves: 129P2/OlaHsd * BALB/c)
|
impaired macrophage chemotaxis
|
J:162714
|
Ccr3tm1Cge/Ccr3tm1Cge
(involves: 129S4/SvJae * BALB/c)
|
impaired eosinophil chemotaxis
|
J:74509
|
increased mast cell degranulation
|
J:74509
|
Ccr5tm1Blck/Ccr5tm1Blck
(B6.129P2-Ccr5tm1Blck)
|
abnormal cellular extravasation
|
J:104744
|
abnormal leukocyte adhesion
|
J:104744
|
Ccr5tm1Kuz/Ccr5tm1Kuz
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired macrophage chemotaxis
|
J:153059,
J:84243,
J:64293
|
Ccr5tm1Sush/Ccr5tm1Sush
(B6.129P2-Ccr5tm1Sush)
|
decreased T cell proliferation
|
J:94937
|
Ccr6tm1(EGFP)Irw/Ccr6tm1(EGFP)Irw
(involves: 129S6/SvEvTac * C57BL/6)
|
impaired B cell migration
|
J:120122
|
increased T cell proliferation
|
J:85086
|
Ccr7tm1Rfor/Ccr7tm1Rfor
(involves: 129P2/OlaHsd * BALB/c)
|
abnormal leukocyte migration
|
J:57976
|
impaired B cell migration
|
J:57976
|
Ccr7tm1Rfor/Ccr7tm1Rfor
(B6.129P2-Ccr7tm1Rfor)
|
abnormal leukocyte migration
|
J:93960,
J:110910
|
Ccr7tm1Rfor/Ccr7tm1Rfor
(involves: 129P2/OlaHsd)
|
abnormal dendritic cell chemotaxis
|
J:223508
|
Ccr7tm1Rfor/Ccr7tm1Rfor Tg(DO11.10)10Dlo/?
(involves: 129P2/OlaHsd * BALB/c * C3H * C57BL/6)
|
abnormal cell migration
|
J:123482
|
abnormal leukocyte migration
|
J:123482
|
Ccr10tm1Cge/Ccr10tm1Cge
(C.129S4-Ccr10tm1Cge)
|
abnormal leukocyte migration
|
J:140728
|
Ccrl2tm1Ssoz/Ccrl2tm1Ssoz
(B6.129-Ccrl2tm1Ssoz)
|
abnormal dendritic cell chemotaxis
|
J:165873
|
Ccstm1Pcw/Ccstm1Pcw
(involves: 129S1/Sv)
|
increased cellular sensitivity to oxidative stress
|
J:80627
|
Ccser2em1Skpk/Ccser2em1Skpk
(C57BL/6N-Ccser2em1Skpk)
|
abnormal neuronal migration
|
J:333716
|
Cct2em2Tiwata/Cct2em2Tiwata
(involves: C57BL/6J)
|
abnormal photoreceptor connecting cilium morphology
|
J:358007
|
Cct6bem1Jsha/Cct6bem1Jsha
(involves: C57BL/6)
|
abnormal sperm flagellum morphology
|
J:307593
|
decreased sperm progressive motility
|
J:307593
|
teratozoospermia
|
J:307593
|
Cd2aptm1Shaw/Cd2ap+
(Not Specified)
|
increased mesangial cell number
|
J:84748
|
Cd2aptm1Shaw/Cd2aptm1Shaw
(involves: 129X1/SvJ)
|
decreased T cell proliferation
|
J:57971
|
increased mesangial cell number
|
J:57971
|
Cd2bp2tm1.1Tbh/Cd2bp2tm1.1Tbh Tg(Mx1-cre)1Cgn/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * CBA/J)
|
impaired macrophage phagocytosis
|
J:283435
|
Cd2bp2tm1.1Tbh/Cd2bp2tm1.1Tbh Tg(NPHS2-cre)295Lbh/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL)
|
increased mesangial cell number
|
J:283435
|
Cd3em1Btlr/Cd3em1Btlr
(C57BL/6J-Cd3em1Btlr)
|
increased T cell apoptosis
|
J:132486
|
Cd3gtm1.1Cage/Cd3gtm1.1Cage
(B6.129P2-Cd3gtm1.1Cage)
|
increased T cell apoptosis
|
J:153813
|
Cd3gtm1Amk/Cd3gtm1Amk
(involves: 129P2/OlaHsd)
|
abnormal T cell proliferation
|
J:77504
|
Cd4tm1Litt/Cd4tm1Litt
(involves: 129S2/SvPas)
|
decreased T cell proliferation
|
J:50435
|
Cd4tm1Litt/Cd4tm1Nik Tg(Lck-cre)3778Nik/0
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:73479
|
Cd4tm1Litt/Cd4tm1Nik Tg(Lck-cre)3785Nik/0
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased T cell apoptosis
|
J:73479
|
increased T cell proliferation
|
J:73479
|
Cd4tm1Litt/Cd4tm1Nik Tg(Lck-icre)3779Nik/0
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:73479
|
Cd5tm1.1Chra/Cd5tm1.1Chra
(involves: C57BL/6 * FVB/N)
|
decreased T cell proliferation
|
J:189919
|
increased T cell proliferation
|
J:189919
|
Cd5tm1.1Chra/Cd5tm1.1Chra Tg(Tcra2D2,Tcrb2D2)1Kuch/0
(involves: C57BL/6 * FVB/N)
|
decreased T cell proliferation
|
J:189919
|
Cd5tm1Cgn/Cd5tm1Cgn
(B6.129P2-Cd5tm1Cgn)
|
increased T cell proliferation
|
J:189919
|
Cd6tm1Linf/Cd6tm1Linf
(D1.Cg-Cd6tm1Linf)
|
decreased B cell proliferation
|
J:238478
|
Cd8am2Btlr/Cd8am2Btlr
(C57BL/6J-Cd8am2Btlr)
|
increased CD8-positive, alpha-beta memory T cell proliferation
|
J:236677
|
Cd9tm1Mek/Cd9tm1Mek
(involves: 129/Sv * C57BL/6)
|
abnormal oocyte morphology
|
J:260669
|
Cd19tm1(cre)Cgn/Cd19+ Ctnnbl1tm1.1Crad/Ctnnbl1tm1.1Crad
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
decreased B cell proliferation
|
J:232010
|
Cd19tm1(cre)Cgn/Cd19+ Ell2tm1.1Cmil/Ell2tm1.1Cmil
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6)
|
abnormal endoplasmic reticulum morphology
|
J:234692
|
Cd19tm1(cre)Cgn/Cd19+ Ep300tm2Reck/Ep300+
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:147840
|
increased B cell apoptosis
|
J:147840
|
Cd19tm1(cre)Cgn/Cd19+ Gt(ROSA)26Sortm1(ITK/SYK)Jrld/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd)
|
increased T cell proliferation
|
J:160931
|
Cd19tm1(cre)Cgn/Cd19+ Gt(ROSA)26Sortm2(CARD11*L225LI)Jrld/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd)
|
increased B cell proliferation
|
J:228288
|
Cd19tm1(cre)Cgn/Cd19+ Gt(ROSA)26Sortm4(Ikbkb)Rsky/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell apoptosis
|
J:113365
|
increased cell proliferation
|
J:113365
|
Cd19tm1(cre)Cgn/Cd19+ Igbp1tm1Imku/Y
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:74619
|
Cd19tm1(cre)Cgn/Cd19+ Ikbkbtm1Cgn/Ikbkbtm1.1Cgn
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:79132
|
Cd19tm1(cre)Cgn/Cd19+ Ikbkbtm2Mka/Ikbkbtm2Mka
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:82995
|
increased B cell apoptosis
|
J:82995
|
Cd19tm1(cre)Cgn/Cd19+ Ikbkgtm1.1Mpa/Y
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:79132
|
Cd19tm1(cre)Cgn/Cd19+ Inpp5dtm1Rav/Inpp5dtm1Rav Ptentm1Hwu/Ptentm1Hwu
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
increased B cell proliferation
|
J:166155
|
Cd19tm1(cre)Cgn/Cd19+ Map3k7tm1Aki/Map3k7tm1.1Aki
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:112597
|
Cd19tm1(cre)Cgn/Cd19+ Mcl1tm2Sjk/Mcl1tm3Sjk
(involves: 129P2/OlaHsd * 129X1/SvJ)
|
increased B cell apoptosis
|
J:86906
|
Cd19tm1(cre)Cgn/Cd19+ Myd88em1.1Rsky/Myd88em1.1Rsky
(involves: C57BL/6NTac)
|
increased B cell proliferation
|
J:308792
|
Cd19tm1(cre)Cgn/Cd19+ Ptentm1Hwu/Ptentm1Hwu
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
increased B cell apoptosis
|
J:83213
|
increased B cell proliferation
|
J:155314,
J:83213
|
Cd19tm1(cre)Cgn/Cd19+ Ptpn6tm1Rsky/Ptpn6tm1Rsky
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:123568
|
Cd19tm1(cre)Cgn/Cd19+ Slc3a2tm1.1Mgin/Slc3a2tm1.1Mgin
(involves: 129 * C57BL/6 * SJL)
|
decreased B cell proliferation
|
J:148000
|
Cd19tm1(cre)Cgn/Cd19+ Tnfaip3tm1.1Awai/Tnfaip3tm1.1Awai
(involves: 129P2/OlaHsd)
|
increased B cell proliferation
|
J:175422
|
Cd19tm1(cre)Cgn/Cd19+ Tnfaip3tm2Ama/Tnfaip3+
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell apoptosis
|
J:163917
|
Cd19tm1(cre)Cgn/Cd19+ Ube2ntm1Aki/Ube2ntm1Aki
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:112287
|
increased B cell apoptosis
|
J:112287
|
Cd19tm1(cre)Cgn/Cd19+ Wacem2Cya/Wacem2Cya
(B6.Cg-Cd19tm1(cre)Cgn Wacem2Cya)
|
abnormal epigenetic regulation of gene expression
|
J:345327
|
decreased B cell proliferation
|
J:345327
|
Cd19tm1Tft/Cd19tm1Tft
(Not Specified)
|
decreased B cell proliferation
|
J:27236
|
Cd19tm1Tft/Cd19tm1Tft
(involves: 129 * C57BL/6)
|
decreased B cell proliferation
|
J:71174
|
Cd19tm1Tft/Cd19tm1Tft Lyntm1Sor/Lyntm1Sor
(involves: 129S4/SvJaeSor * C57BL/6)
|
decreased B cell proliferation
|
J:71174
|
Cd22tm1.1(CD22)Lnit/Cd22tm1.1(CD22)Lnit
(involves: 129S4/SvJae)
|
impaired B cell migration
|
J:189017
|
Cd22tm1Eac/Cd22tm1Eac
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal B cell proliferation
|
J:37451,
J:132991
|
increased B cell apoptosis
|
J:132991
|
Cd22tm1Tft/Cd22tm1Tft
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:92736
|
Cd22tm2Tft/Cd22tm2Tft
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
decreased B cell proliferation
|
J:92736
|
increased B cell proliferation
|
J:92736
|
Cd22tm2Tft/Cd22tm2Tft
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased B cell proliferation
|
J:208364
|
increased activation-induced B cell apoptosis
|
J:208364
|
Cd22tm3Lnit/Cd22tm3Lnit
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
decreased cell migration
|
J:198790
|
increased B cell apoptosis
|
J:198790
|
Cd22tm3Tft/Cd22tm3Tft
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
decreased B cell proliferation
|
J:92736
|
increased B cell proliferation
|
J:92736
|
Cd27tm1Jbo/Cd27tm1Jbo
(B6.129P2-Cd27tm1Jbo)
|
increased T cell apoptosis
|
J:198200
|
Cd28tm1Jmg/Cd28tm1Mak
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
decreased T cell proliferation
|
J:149888,
J:124570
|
Cd28tm1Ltu/Cd28tm1Ltu Foxp3tm4(YFP/icre)Ayr/Foxp3+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased T cell proliferation
|
J:194503
|
Cd28tm1Mak/Cd28tm1Mak
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:14194
|
Cd28tm1Mak/Cd28tm1Mak
(NOD.129S2-Cd28tm1Mak)
|
increased T cell proliferation
|
J:93421
|
Cd28tm1Mak/Cd28tm1Mak
(involves: 129S2/SvPas)
|
decreased T cell proliferation
|
J:205441,
J:130882,
J:123989
|
Cd28tm1Mak/Cd28tm1Mak
(involves: 129S2/SvPas * NOD)
|
decreased T cell proliferation
|
J:35353
|
Cd28tm1Mak/Cd28tm1Mak
(involves: 129S2/SvPas * C57BL/6)
|
decreased T cell proliferation
|
J:149888
|
increased T cell apoptosis
|
J:149888
|
Cd28tm1Mak/Cd28tm1Mak Tg(Cd4-cre)1Cwi/? Traf6tm2Ywc/Traf6tm2Ywc
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:130882
|
Cd28tm1Mak/Cd28tm1Mak Tg(TcrLCMV)327Sdz/0
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
decreased splenocyte proliferation
|
J:123989
|
decreased T cell proliferation
|
J:123989
|
Cd28tm1Pjl/Cd28tm1Pjl
(involves: 129P2/OlaHsd * C57BL/6)
|
increased splenocyte proliferation
|
J:83722
|
Cd28tm1Pjl/Cd28tm1Pjl Tg(DO11.10)10Dlo/0
(involves: 129P2/OlaHsd * BALB/c * C3H * C57BL/6)
|
abnormal T cell proliferation
|
J:25536
|
Cd28tm1Pjl/Cd28tm1Pjl Tnfrsf9tm1Byk/Tnfrsf9tm1Byk
(either: B6.Cg-Cd28tm1Pjl Tnfrsf9tm1Byk or C.Cg-Cd28tm1Pjl Tnfrsf9tm1Byk)
|
decreased splenocyte proliferation
|
J:83722
|
Cd28tm1Shr/Cd28tm1Shr
(involves: 129S4/SvJae * BALB/c * C57BL/6)
|
decreased T cell proliferation
|
J:68642
|
Cd28tm1Shr/Cd28tm1Shr Ctla4tm1Shr/Ctla4tm1Shr
(C.129S4-Cd28tm1Shr Ctla4tm1Shr)
|
decreased T cell proliferation
|
J:68642
|
Cd34tm1Szk/Cd34tm1Szk
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cell proliferation
|
J:121305
|
Cd36tm1Frm/Cd36tm1Frm
(B6.129S4-Cd36tm1Frm)
|
impaired macrophage phagocytosis
|
J:100140
|
Cd36tm1Mfe/Cd36tm1Mfe
(involves: 129S1/Sv * C57BL/6)
|
increased cardiac muscle cell glucose uptake
|
J:83611
|
Cd36tm1Mfe/Cd36tm1Mfe
(involves: 129S1/Sv)
|
abnormal macrophage chemotaxis
|
J:89664
|
decreased adipocyte glucose uptake
|
J:220343
|
decreased skeletal muscle cell glucose uptake
|
J:220343
|
Cd36tm2.1Mfe/Cd36tm2.1Mfe A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(B6.Cg-Cd36tm2.1Mfe A1cfTg(Myh6-cre/Esr1*)1Jmk)
|
decreased fatty acid oxidation
|
J:225392
|
Cd38tm1Lnd/Cd38tm1Lnd
(NOD.129P2(B6)-Cd38tm1Lnd/LtJ)
|
increased T cell apoptosis
|
J:108097
|
Cd38tm1Lnd/Cd38tm1Lnd
(B6.129P2-Cd38tm1Lnd)
|
increased pancreatic islet cell apoptosis
|
J:116576
|
Cd40lgtm1Flv/Cd40lgtm1Flv
(involves: 129S2/SvPas * C57BL/6)
|
abnormal osteoclast differentiation
|
J:120087
|
Cd40lgtm1Imx/Y
(B6.129S2-Cd40lgtm1Imx/J)
|
abnormal leukocyte adhesion
|
J:108988
|
Cd44tm1.1Ugu/Cd44tm1.1Ugu
(SJL.129(Cg)-Cd44tm1.1Ugu)
|
decreased T cell proliferation
|
J:199279
|
Cd44tm1Hbg/Cd44tm1Hbg
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:68069
|
Cd44tm1Hbg/Cd44tm1Hbg
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoclast differentiation
|
J:101563
|
Cd44tm1Hbg/Cd44tm1Hbg Tg(TNF)197Gkl/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal osteoclast differentiation
|
J:97992
|
Cd44tm1Mak/Cd44+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal leukocyte migration
|
J:99032
|
Cd44tm1Mak/Cd44tm1Mak
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell morphology
|
J:105319
|
abnormal cell physiology
|
J:72658
|
abnormal leukocyte migration
|
J:99032
|
abnormal mitochondrial crista morphology
|
J:105319
|
decreased fibroblast proliferation
|
J:105319
|
increased mitochondrial size
|
J:105319
|
Cd44tm1Mak/Cd44tm1Mak
(B6.129P2-Cd44tm1Mak)
|
abnormal leukocyte migration
|
J:108245
|
decreased activation-induced cell death of T cells
|
J:69351
|
decreased sensitivity to induced cell death
|
J:69351
|
impaired macrophage phagocytosis
|
J:111216
|
Cd44tm2.1Ugu/Cd44tm2.1Ugu
(B6.129-Cd44tm2.1Ugu)
|
decreased T cell proliferation
|
J:199279
|
Cd44tm2Kmz/Cd44tm2Kmz
(involves: BALB/c * DBA/1)
|
abnormal leukocyte adhesion
|
J:114317
|
impaired leukocyte tethering or rolling
|
J:114317
|
Cd44tm2Kmz/Cd44tm2Kmz Selltm2Hyn/Selltm2Hyn
(involves: 129S2/SvPas * BALB/c * DBA/1)
|
abnormal leukocyte adhesion
|
J:114317
|
impaired leukocyte tethering or rolling
|
J:114317
|
Cd47tm1Fpl/Cd47tm1Fpl
(involves: 129S7/SvEvBrd)
|
abnormal mitochondrial physiology
|
J:133700
|
Cd47tm1Fpl/Cd47tm1Fpl
(B6.129S7-Cd47tm1Fpl)
|
impaired neutrophil chemotaxis
|
J:36489
|
impaired neutrophil phagocytosis
|
J:36489
|
Cd47tm1Fpl/Cd47tm1Fpl
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:147367
|
Cd48tm1Rsr/Cd48tm1Rsr
(B6.129S4-Cd48tm1Rsr)
|
decreased T cell proliferation
|
J:53718
|
Cd59atm1Bpm/Cd59atm1Bpm
(B6.129-Cd59atm1Bpm)
|
decreased B cell proliferation
|
J:119703
|
increased renal tubule apoptosis
|
J:92414
|
increased T cell proliferation
|
J:122201
|
Cd59btm1Jha/Cd59btm1Jha
(involves: 129/Sv * C57BL/6)
|
abnormal male germ cell morphology
|
J:82330
|
abnormal sperm head morphology
|
J:108100
|
absent sperm head
|
J:108100
|
asthenozoospermia
|
J:82330
|
increased male germ cell apoptosis
|
J:108100
|
multinucleated giant male germ cells
|
J:82330,
J:108100
|
necrospermia
|
J:108100
|
oligozoospermia
|
J:82330,
J:108100
|
Cd69tm1Naka/Cd69tm1Naka
(C.129P2-Cd69tm1Naka)
|
impaired neutrophil chemotaxis
|
J:84940
|
Cd72c/Cd72c
(involves: C57BL/6 * MRL)
|
increased B cell proliferation
|
J:204782
|
Cd72tm1Jrp/Cd72tm1Jrp
(either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6))
|
increased B cell proliferation
|
J:76990
|
Cd72tm1Tsub/Cd72tm1Tsub
(involves: C57BL/6J)
|
increased B cell proliferation
|
J:204782
|
Cd74tm1Eae/Cd74tm1Eae
(involves: 129S2/SvPas)
|
decreased B cell proliferation
|
J:113050,
J:132865
|
decreased cell proliferation
|
J:147772
|
Cd74tm1Liz/Cd74tm1Liz
(involves: 129S/SvEv * C57BL/6J)
|
decreased T cell proliferation
|
J:72243
|
Cd74tm1Liz/Cd74tm1Liz
(B6.129S-Cd74tm1Liz)
|
decreased T cell proliferation
|
J:28966
|
Cd74tm1Liz/Cd74tm1Liz
(involves: 129S/SvEv * BALB/c * C57BL)
|
abnormal T cell proliferation
|
J:110927
|
Cd74tm1Liz/Cd74tm1Liz
(involves: 129S/SvEv * C57BL * C57BL/10 * C57BR)
|
abnormal T cell proliferation
|
J:110927
|
Cd74tm2Liz/Cd74tm1Liz
(involves: 129S/SvEv * C57BL/6)
|
increased T cell proliferation
|
J:28966
|
Cd79atm1(cre)Reth/Cd79a+ Ctnnbl1tm1.1Crad/Ctnnbl1tm1.1Crad
(involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL)
|
abnormal B cell proliferation
|
J:232010
|
decreased B cell proliferation
|
J:232010
|
Cd79atm1(cre)Reth/Cd79a+ Huwe1tm1.1Mak/Y
(B6.Cg-Cd79atm1(cre)Reth Huwe1tm1.1Mak)
|
decreased B cell proliferation
|
J:181705
|
increased B cell apoptosis
|
J:181705
|
Cd79atm1(cre)Reth/Cd79a+ Nr4a1tm1Pcn/Nr4a1tm1Pcn
(involves: 129 * BALB/c)
|
increased B cell proliferation
|
J:306652
|
Cd79atm1(cre)Reth/Cd79a+ Nr4a1tm1Pcn/Nr4a1tm1Pcn Nr4a3em1Juz/Nr4a3em1Juz
(involves: 129 * BALB/c * C57BL/6)
|
decreased B cell apoptosis
|
J:306652
|
increased B cell proliferation
|
J:306652
|
Cd79atm1(cre)Reth/Cd79a+ Orai1tm1Smua/Orai1tm1Smua Orai3em1.1Treb/Orai3em1.1Treb
(involves: BALB/c * C57BL/6J * C57BL/6N)
|
decreased B cell proliferation
|
J:345485
|
Cd79atm1(cre)Reth/Cd79a+ Wastm1.1Ldn/Was+
(involves: BALB/c * C57BL/6)
|
abnormal B cell proliferation
|
J:182528
|
Cd79atm6Cgn/Cd79atm6Cgn
(involves: C57BL/6)
|
abnormal cell cycle
|
J:113407
|
abnormal mitosis
|
J:113407
|
decreased B cell proliferation
|
J:113407
|
Cd79btm3Mnz/Cd79btm3Mnz
(involves: 129/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:128768
|
Cd80tm1Shr/Cd80tm1Shr
(involves: 129S4/SvJae)
|
decreased B cell proliferation
|
J:74662
|
Cd80tm1Shr/Cd80tm1Shr Cd86tm1Shr/Cd86tm1Shr
(B6.129S4-Cd80tm1Shr Cd86tm1Shr)
|
decreased T cell proliferation
|
J:57613
|
Cd80tm1Shr/Cd80tm1Shr Cd86tm2Shr/Cd86tm2Shr
(involves: 129S4/SvJae)
|
abnormal T cell proliferation
|
J:57090
|
Cd80tm1Shr/Cd80tm1Shr Cd86tm2Shr/Cd86tm2Shr
(129.SJL-Cd86tm2Shr)
|
decreased cell proliferation
|
J:78992
|
Cd80tm1Shr/Cd80tm1Shr Cd86tm2Shr/Cd86tm2Shr
(involves: 129S4/SvJae * C57BL/6J * SJL)
|
decreased cell proliferation
|
J:78992
|
Cd80tm1Shr/Cd80tm1Shr Cd86tm2Shr/Cd86tm2Shr Ctla4tm1Shr/Ctla4tm1Shr
(involves: 129S4/SvJae * BALB/c)
|
increased T cell proliferation
|
J:57090
|
Cd81tm1Geha/Cd81tm1Geha
(involves: 129S4/SvJae * C57BL/6)
|
increased B cell proliferation
|
J:43975
|
Cd81tm1Tmiy/Cd81tm1Tmiy
(involves: 129/Sv * C57BL/6)
|
abnormal T cell proliferation
|
J:41830
|
decreased B cell proliferation
|
J:41830
|
increased B cell proliferation
|
J:41830
|
Cd82tm1.1Xaz/Cd82tm1.1Xaz
(B6NCr.Cg-Cd82tm1.1Xaz)
|
abnormal vascular endothelial cell migration
|
J:234155
|
Cd82tm1Kjbr/Cd82tm1Kjbr
(Not Specified)
|
abnormal cellular extravasation
|
J:326451
|
abnormal macrophage differentiation
|
J:326451
|
impaired leukocyte tethering or rolling
|
J:326451
|
Cd83lcd4/Cd83lcd4
(involves: C57BL/6J)
|
decreased T cell proliferation
|
J:92721
|
Cd86tm1Shr/Cd86tm1Shr
(NOD.129S4-Cd86tm1Shr)
|
abnormal T cell proliferation
|
J:142046
|
decreased T cell proliferation
|
J:93421
|
Cd86tm1Shr/Cd86tm1Shr
(B6.129S4-Cd86tm1Shr)
|
decreased T cell proliferation
|
J:57613
|
Cd93tm1Mbo/Cd93tm1Mbo
(either: 129/Sv or B6.129-Cd93tm1Mbo or (involves: 129/Sv * C57BL/6))
|
impaired macrophage phagocytosis
|
J:88610
|
Cd99l2tm1.1Dvst/Cd99l2tm1.1Dvst Tg(Tek-cre)1Ywa/0
(involves: 129S6/SvEvTac * BALB/c * C57BL/6)
|
abnormal cellular extravasation
|
J:193021
|
cellular phenotype
|
J:193021
|
Cd99l2tm1.2Dvst/Cd99l2tm1.2Dvst
(involves: 129S6/SvEvTac * BALB/c * C57BL/6)
|
abnormal cellular extravasation
|
J:193021
|
cellular phenotype
|
J:193021
|
Cd151tm1Lka/Cd151tm1Lka
(C57BL/6-Cd151tm1Lka)
|
abnormal T cell proliferation
|
J:91605
|
decreased keratinocyte migration
|
J:91605
|
Cd151tm1Mhe/Cd151tm1Mhe
(B6.129S-Cd151tm1Mhe)
|
abnormal vascular endothelial cell migration
|
J:141595
|
Cd151tm1Nki/Cd151tm1Nki
(involves: 129P2/OlaHsd * FVB/N)
|
increased mesangial cell number
|
J:114988
|
Cd151tm2Nki/Cd151tm2Nki
(FVB.129P2-Cd151tm2Nki)
|
decreased keratinocyte proliferation
|
J:205736
|
Cd151tm2Nki/Cd151tm2Nki Itga3tm1Son/Itga3+ Krt14tm1(cre)Wbm/?
(FVB.129P2-Cd151tm2Nki Itga3tm1Son Krt14tm1(cre)Wbm)
|
decreased keratinocyte proliferation
|
J:205736
|
Cd151tm2Nki/Cd151tm2Nki Krt14tm1(cre)Wbm/?
(FVB.129P2-Cd151tm2Nki Krt14tm1(cre)Wbm)
|
decreased keratinocyte proliferation
|
J:205736
|
increased keratinocyte migration
|
J:205736
|
Cd163tm1(KOMP)Vlcg/Cd163tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal aerobic respiration
|
J:224919
|
abnormal macrophage chemotaxis
|
J:224919
|
abnormal skeletal muscle satellite cell proliferation
|
J:224919
|
Cd200tm1Jods/Cd200tm1Jods
(C57BL/6-Cd200tm1Jods)
|
increased apoptosis
|
J:79906
|
Cd209atm1.1Cfg/Cd209atm1.1Cfg
(involves: C57BL/6)
|
increased T cell proliferation
|
J:217719
|
Cd209btm1.1Cfg/Cd209btm1.1Cfg
(involves: C57BL/6)
|
impaired macrophage phagocytosis
|
J:288225
|
Cd209btm1Anjm/Cd209btm1Anjm
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired macrophage phagocytosis
|
J:94698
|
Cd209dtm1.1Cfg/Cd209dtm1.1Cfg
(involves: C57BL/6)
|
increased B cell proliferation
|
J:217719
|
Cd226tm1.1Cln/Cd226tm1.1Cln
(B6.129P2-Cd226tm1.1Cln)
|
decreased T cell proliferation
|
J:159749
|
Cd226tm1.1Cln/Cd226tm1.1Cln Tg(TcraTcrb)1100Mjb/0
(B6.Cg-Cd226tm1.1Cln Tg(TcraTcrb)1100Mjb)
|
decreased T cell proliferation
|
J:159749
|
Cd247tm1Mhu/Cd247tm1Mhu
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased splenocyte proliferation
|
J:15579
|
decreased T cell proliferation
|
J:15579
|
Cd247tm1Tks/Cd247tm1Tks
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal T cell proliferation
|
J:15271
|
Cd247tm2.1Lov/Cd247tm2.1Lov
(Not Specified)
|
decreased thymocyte apoptosis
|
J:192915
|
Cd274tm1Lpc/Cd274tm1Lpc
(B6.129S-Cd274tm1Lpc)
|
decreased T cell apoptosis
|
J:89781
|
Cd274tm1Lpc/Cd274tm1Lpc
(involves: 129S/SvEv * C57BL/6)
|
decreased T cell apoptosis
|
J:136330
|
Cd274tm1Lpc/Cd274tm1Lpc
(C.129S-Cd274tm1Lpc)
|
increased T cell proliferation
|
J:165841
|
Cd276tm1Mak/Cd276tm1Mak
(involves: 129P2/OlaHsd * C57BL/6)
|
increased T cell proliferation
|
J:84973
|
Cd300c2tm1Shib/Cd300c2tm1Shib
(B6.Cg-Cd300c2tm1Shib)
|
increased B cell proliferation
|
J:177613
|
Cdatm1d(EUCOMM)Wtsi/Cdatm1d(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6J * C57BL/6N)
|
abnormal cell physiology
|
J:332259
|
chromosomal instability
|
J:332259
|
elevated level of mitotic sister chromatid exchange
|
J:332259
|
Cdc7tm1Hmas/Cdc7tm1Hmas Tg(EF1A-Cdc7)DKO28Hmas/0
(involves: 129S/Sv * C57BL/6)
|
abnormal cell cycle
|
J:85942
|
arrest of male meiosis
|
J:85942
|
decreased DNA replication
|
J:85942
|
multinucleated giant male germ cells
|
J:85942
|
Cdc14aem1Jgao/Cdc14aem1Jgao
(CBA/CaJ-Cdc14aem1Jgao)
|
abnormal sperm head morphology
|
J:301219
|
abnormal sperm nucleus morphology
|
J:301219
|
absent sperm head
|
J:301219
|
arrest of male meiosis
|
J:301219
|
asthenozoospermia
|
J:301219
|
coiled sperm flagellum
|
J:301219
|
decreased male germ cell number
|
J:301219
|
decreased sperm progressive motility
|
J:301219
|
paternal effect
|
J:301219
|
teratozoospermia
|
J:301219
|
Cdc14aem1Tbf/Cdc14aem1Tbf
(involves: C57BL/6J)
|
oligozoospermia
|
J:257652
|
Cdc14atm1a(EUCOMM)Hmgu/Cdc14atm1b(EUCOMM)Hmgu
(involves: C57BL/6N * FVB)
|
oligozoospermia
|
J:257652
|
teratozoospermia
|
J:257652
|
Cdc14atm1b(EUCOMM)Hmgu/Cdc14atm1b(EUCOMM)Hmgu
(involves: C57BL/6N * FVB)
|
oligozoospermia
|
J:257652
|
teratozoospermia
|
J:257652
|
Cdc14atm1d(EUCOMM)Hmgu/Cdc14atm1d(EUCOMM)Hmgu
(involves: C57BL/6N * FVB)
|
oligozoospermia
|
J:257652
|
teratozoospermia
|
J:257652
|
Cdc14btm1.1Mama/Cdc14btm1.1Mama
(Not Specified)
|
cellular phenotype
|
J:206116
|
Cdc14btm1.2Pzg/Cdc14btm1.2Pzg
(B6.129P2-Cdc14btm1.2Pzg)
|
abnormal DNA repair
|
J:170763
|
cellular phenotype
|
J:170763
|
early cellular replicative senescence
|
J:170763
|
Cdc20Gt(XE368)Byg/Cdc20Gt(XE368)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal chromosome morphology
|
J:121535
|
Cdc20Gt(XE368)Byg/Cdc20Gt(XE368)Byg Pttg1tm1Pzg/Pttg1tm1Pzg
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6)
|
abnormal chromosome morphology
|
J:121535
|
Cdc20Gt(XE368)Byg/Cdc20tm1Jvd
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6)
|
abnormal female meiosis
|
J:165500
|
abnormal male germ cell morphology
|
J:165500
|
abnormal oocyte morphology
|
J:165500
|
aneuploidy
|
J:165500
|
maternal effect
|
J:165500
|
Cdc20tm1.1Mama/Cdc20tm1.1Mama Pttg1tm1.1Kna/Pttg1tm1.1Kna
(involves: 129 * C57BL/6 * CD-1 * SJL)
|
abnormal mitosis
|
J:167609
|
Cdc20tm1.1Mama/Cdc20tm1.2Mama Polr2atm1(cre/ERT2)Bbd/Polr2a+
(involves: 129/Sv * BALB/cJ * C57BL/6 * CD-1 * SJL)
|
abnormal mitosis
|
J:167609
|
decreased cell proliferation
|
J:167609
|
Cdc20tm1.1Pzg/Cdc20+
(involves: 129S7/SvEvBrd * C57BL/6)
|
aneuploidy
|
J:150421
|
Cdc20tm1.1Pzg/Cdc20tm1.1Pzg
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell death
|
J:150421
|
abnormal mitosis
|
J:150421
|
aneuploidy
|
J:150421
|
decreased cell proliferation
|
J:150421
|
increased embryonic tissue cell apoptosis
|
J:150421
|
Cdc23em1Lwa/Cdc23em1Lwa
(C57BL/6N-Cdc23em1Lwa)
|
abnormal female meiosis I arrest
|
J:344361
|
Cdc25am1Rfp/Cdc25am1Rfp
(multiple strains)
|
abnormal cell cycle checkpoint function
|
J:80142
|
increased cell proliferation
|
J:80142
|
Cdc25atm1.1Hpw/Cdc25atm1.1Hpw
(involves: 129X1/SvJ * C57BL/6)
|
increased apoptosis
|
J:145768
|
Cdc25atm1Dvb/Cdc25atm1Dvb
(involves: 129)
|
abnormal centrosome morphology
|
J:144548
|
abnormal mitosis
|
J:144548
|
aneuploidy
|
J:144548
|
increased cellular sensitivity to gamma-irradiation
|
J:144548
|
Cdc25atm1Hpw/Cdc25atm1.1Hpw Cdc25btm1Pjd/Cdc25btm1Pjd Cdc25ctm1Hpw/Cdc25ctm1Hpw Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal enterocyte differentiation
|
J:169457
|
abnormal small intestinal crypt cell proliferation
|
J:169457
|
increased enterocyte apoptosis
|
J:169457
|
Cdc25atm1Hpw/Cdc25atm1.1Hpw Cdc25btm1Pjd/Cdc25btm1Pjd Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal enterocyte differentiation
|
J:169457
|
abnormal small intestinal crypt cell proliferation
|
J:169457
|
increased enterocyte apoptosis
|
J:169457
|
Cdc25atm1Kiyo/Cdc25a+ Tg(MMTV-Erbb2)NK1Mul/?
(involves: 129/Sv * C57BL/6 * FVB/N)
|
decreased cell proliferation
|
J:123144
|
Cdc25btm1Pjd/Cdc25btm1Pjd
(Not Specified)
|
abnormal female meiosis
|
J:87011
|
abnormal oocyte morphology
|
J:87011
|
Cdc42tm1.1Ayam/Cdc42tm1.1Ayam Tg(Prrx1-cre)1Cjt/0
(involves: 129P2/OlaHsd * C57BL/6 * ICR * SJL)
|
abnormal interdigital cell death
|
J:184022
|
Cdc42tm1.1Rac/Cdc42tm1.1Rac Tg(GFAP-cre)25Mes/0
(involves: 129P2/OlaHsd * FVB/N)
|
absent brain ependyma motile cilia
|
J:197886
|
Cdc42tm1.1Rac/Cdc42tm1.1Rac Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL)
|
abnormal cell nucleus morphology
|
J:197886
|
abnormal neuronal precursor proliferation
|
J:197886
|
Cdc42tm1Brak/Cdc42+ Rab8atm1.1Aha/Rab8a+ Tg(Vil1-cre)997Gum/0
(involves: C57BL/6J * SJL)
|
abnormal cellular glucose uptake
|
J:184563
|
Cdc42tm1Brak/Cdc42tm1Brak Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6)
|
increased small intestinal crypt cell apoptosis
|
J:184563
|
Cdc42tm1Brak/Cdc42tm1Brak Tg(Vil1-cre)997Gum/0
(involves: C57BL/6J * SJL)
|
abnormal intestinal goblet cell morphology
|
J:184563
|
increased small intestinal crypt cell apoptosis
|
J:184563
|
Cdc42tm1Fwa/Cdc42tm1Fwa
(involves: 129S6/SvEvTac)
|
abnormal actin cytoskeleton morphology
|
J:63261
|
Cdc42ep1tm1Yxz/Cdc42ep1tm1Yxz
(B6.Cg-Cdc42ep1tm1Yzh)
|
decreased cell migration
|
J:310382
|
Cdc45tm1Dta/Cdc45tm1Dta
(involves: 129S4/SvJae * C57BL/6)
|
absent inner cell mass proliferation
|
J:70008
|
Cdc73Gt(RRE190)Byg/Cdc73Gt(RRE190)Byg
(involves: 129P2/OlaHsd)
|
absent inner cell mass proliferation
|
J:135255
|
absent trophectoderm cell proliferation
|
J:135255
|
Cdc73tm1Btt/Cdc73tm1Btt Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
decreased cell proliferation
|
J:135255
|
increased apoptosis
|
J:135255
|
increased fibroblast apoptosis
|
J:135255
|
Cdca7em1Ldax/Cdca7em1Ldax Tg(HBA1-GFP)1Ew/0
(FVB/NJ-Cdca7em1Ldax Tg(HBA1-GFP)1Ew)
|
abnormal DNA methylation
|
J:345314
|
Cdca8tm1Tatn/Cdca8tm1Tatn
(involves: C57BL/6 * CBA)
|
abnormal cell nucleus morphology
|
J:135988
|
abnormal mitosis
|
J:135988
|
increased apoptosis
|
J:135988
|
increased cell nucleus count
|
J:135988
|
Cdh1tm1Kem/Cdh1tm2.1Kem
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
abnormal cell adhesion
|
J:77170
|
Cdh1tm2.1Mpst/Cdh1tm2.1Mpst
(involves: C57BL/6 * FVB/N)
|
increased trophectoderm apoptosis
|
J:183847
|
Cdh1tm2Kem/Cdh1tm2Kem Tg(Ins2-cre)23Herr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J)
|
increased pancreatic beta cell proliferation
|
J:196410
|
Cdh2tm1Glr/Cdh2tm1Glr Emx1tm1(cre)Krj/Emx1+
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal radial glial cell morphology
|
J:215584
|
Cdh2tm1Glr/Cdh2tm1Glr Olig2tm1(cre)Tmj/Olig2+
(involves: 129S6/SvEvTac)
|
abnormal neuronal migration
|
J:178688
|
Cdh4tm1Semb/Cdh4tm1Semb
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J))
|
increased metanephric mesenchyme apoptosis
|
J:74658
|
Cdh5tm1.1Pec/Cdh5tm1.1Pec
(Not Specified)
|
increased apoptosis
|
J:56509
|
Cdh5tm1Hub/Cdh5tm1Hub
(involves: 129S1/Sv * 129X1/SvJ * BALB/cIco)
|
abnormal cell death
|
J:54177
|
Cdh5tm1Pec/Cdh5tm1Pec
(Not Specified)
|
increased apoptosis
|
J:56509
|
Cdh5tm2Pec/Cdh5tm2Pec
(Not Specified)
|
increased apoptosis
|
J:56509
|
Cdh5tm3(Cdh5/Ctnna1)Dvst/Cdh5tm3(Cdh5/Ctnna1)Dvst
(involves: 129 * C57BL/6)
|
abnormal cellular extravasation
|
J:177191
|
abnormal leukocyte migration
|
J:177191
|
Cdh5tm4(Cdh5/Fkbp,Ptprb/Mtor*)Dvst/Cdh5tm4(Cdh5/Fkbp,Ptprb/Mtor*)Dvst
(involves: C57BL/6)
|
abnormal cellular extravasation
|
J:178759
|
Cdh5tm5Dvst/Cdh5tm5Dvst
(B6.Cg-Cdh5tm5Dvst)
|
abnormal cellular extravasation
|
J:209801
|
Cdh5tm6Dvst/Cdh5tm6Dvst
(B6.Cg-Cdh5tm6Dvst)
|
abnormal cellular extravasation
|
J:209801
|
Cdh23v-2J/Cdh23v-2J
(B6(V)-Cdh23v-2J/J)
|
abnormal inner hair cell kinocilium morphology
|
J:135991
|
abnormal outer hair cell kinocilium morphology
|
J:135991
|
Cdh23v-Alb/Cdh23v-Alb
(involves: C3H/HeJ * C57BL/6)
|
abnormal outer hair cell kinocilium location or orientation
|
J:66698
|
Cdhr5tm1Lex/Cdhr5tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal enterocyte proliferation
|
J:301471
|
Cdip1Gt(IST12371A7)Tigm/Cdip1Gt(IST12371A7)Tigm
(FVB.B6N-Cdip1Gt(IST12371A7)Tigm)
|
decreased apoptosis
|
J:203766
|
Cdk1tm1(Cdk2)Kald/Cdk1+ Cdk2tm1Kald/Cdk2tm1Kald
(involves: 129S1/Sv * C57BL/6)
|
abnormal male meiosis
|
J:141249
|
abnormal spermatocyte morphology
|
J:141249
|
absent oocytes
|
J:141249
|
decreased round spermatid number
|
J:141249
|
increased male germ cell apoptosis
|
J:141249
|
Cdk1tm2.1Kald/Cdk1tm2.1Kald Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129 * C57BL/6 * DBA * SJL)
|
abnormal mitosis
|
J:182141
|
decreased hepatocyte proliferation
|
J:182141
|
polyploidy
|
J:182141
|
Cdk1tm2.1Kald/Cdk1tm2.1Kald Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129 * C57BL/6 * CBA * SJL)
|
abnormal DNA replication
|
J:182141
|
decreased cell proliferation
|
J:182141
|
early cellular replicative senescence
|
J:182141
|
Cdk1tm2.2Kald/Cdk1tm2.2Kald
(involves: 129 * C57BL/6 * FVB/N * SJL)
|
abnormal cell nucleus count
|
J:182141
|
abnormal cell nucleus morphology
|
J:182141
|
Cdk1tm3Kald/Cdk1+ Fbxo43tm1.2Kald/Fbxo43tm1.2Kald Gt(ROSA)26Sortm1(cre/ERT)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL)
|
arrest of male meiosis
|
J:251984
|
azoospermia
|
J:251984
|
increased male germ cell apoptosis
|
J:251984
|
Cdk1tm3Kald/Cdk1+ Tg(Stra8-icre)1Reb/0
(involves: 129 * C57BL/6 * FVB/NJ)
|
arrest of male meiosis
|
J:251984
|
azoospermia
|
J:251984
|
Cdk2tm1.1Jro/Cdk2+
(involves: 129S1/SvlmJ * 129S4/SvJaeSor * C57BL/6)
|
azoospermia
|
J:183801
|
Cdk2tm1.1Jro/Cdk2tm1.1Jro
(involves: 129S1/SvlmJ * 129S4/SvJaeSor * C57BL/6)
|
cellular phenotype
|
J:183801
|
Cdk2tm1Kald/Cdk2tm1Kald
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell cycle
|
J:86203
|
abnormal male meiosis
|
J:86203
|
abnormal oogenesis
|
J:86203
|
absent oocytes
|
J:86203
|
azoospermia
|
J:86203
|
Cdk2tm1Kald/Cdk2tm1Kald
(involves: 129S1/Sv)
|
abnormal male meiosis
|
J:141249
|
decreased hepatocyte proliferation
|
J:141249
|
Cdk2tm1Kald/Cdk2tm1Kald Cdk4tm1Kiyo/Cdk4tm1Kiyo
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell cycle
|
J:108720
|
abnormal fetal cardiomyocyte proliferation
|
J:108720
|
decreased cell proliferation
|
J:108720
|
Cdk2tm1Kald/Cdk2tm1Kald Cdk4tm1Kiyo/Cdk4tm1Kiyo Cdkn1btm1Ako/Cdkn1btm1Ako
(involves: 129S1/Sv * C57BL/6)
|
decreased cell proliferation
|
J:108720
|
Cdk2tm1Sgo/Cdk2tm1Sgo
(involves: 129/Sv * CD-1)
|
abnormal meiosis
|
J:85230
|
abnormal oocyte morphology
|
J:85230
|
Cdk2tm1Sgo/Cdk2tm1Sgo Cdk4tm1Bbd/Cdk4tm1Bbd Cdk6tm1Bbd/Cdk6tm1Bbd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:124678
|
Cdk2tm1Sgo/Cdk2tm1Sgo Cdk4tm2.1Bbd/Cdk4tm2.1Bbd
(involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL)
|
abnormal cell cycle
|
J:125217
|
abnormal fetal cardiomyocyte proliferation
|
J:125217
|
decreased fibroblast proliferation
|
J:125217
|
Cdk2tm1Sgo/Cdk2tm1Sgo Cdk6tm1Bbd/Cdk6tm1Bbd
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal oogenesis
|
J:92529
|
Cdk2ap1tm1Dtw/Cdk2ap1tm1Dtw
(involves: 129S4/SvJae)
|
abnormal cell physiology
|
J:146277
|
Cdk4tm1.1Bbd/Cdk4tm1.1Bbd Tg(Tyr-NRAS*Q61K)1Bee/0
(FVB.Cg-Cdk4tm1.1Bbd Tg(Tyr-NRAS*Q61K)1Bee)
|
abnormal melanocyte proliferation
|
J:222847
|
Cdk4tm1Bbd/Cdk4tm1Bbd
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
abnormal cell cycle
|
J:54534
|
oligozoospermia
|
J:54534
|
Cdk4tm1Kiyo/Cdk4+ Lin9tm1Orc/Lin9+
(involves: 129S1/Sv)
|
abnormal cell cycle
|
J:111333
|
Cdk4tm1Kiyo/Cdk4tm1Kiyo
(involves: 129S1/Sv * C57BL/6)
|
oligozoospermia
|
J:57854
|
Cdk4tm1Kiyo/Cdk4tm1Kiyo
(involves: 129S1/Sv)
|
azoospermia
|
J:111333
|
Cdk4tm1Kiyo/Cdk4tm1Kiyo Lin9tm1Orc/Lin9tm1Orc
(involves: 129S1/Sv)
|
abnormal cell cycle
|
J:111333
|
Cdk4tm2.1Bbd/Cdk4tm2.1Bbd Krastm1Bbd/Krastm2Bbd Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:161780
|
early cellular replicative senescence
|
J:161780
|
Cdk4tm2.2Bbd/Cdk4tm2.1Bbd Krastm1Bbd/Krastm2Bbd Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:161780
|
early cellular replicative senescence
|
J:161780
|
Cdk5r1tm1Lht/Cdk5r1+ Cdk5r2tm1Lht/Cdk5r2tm1Lht
(involves: 129S4/SvJae * C57BL/6)
|
abnormal neuron differentiation
|
J:71181
|
Cdk5r1tm1Lht/Cdk5r1tm1Lht
(involves: 129S4/SvJae)
|
abnormal axon extension
|
J:193542
|
increased cellular glucose import
|
J:204269
|
Cdk5r1tm1Lht/Cdk5r1tm1Lht Cdk5r2tm1Lht/Cdk5r2tm1Lht
(involves: 129S4/SvJae * C57BL/6)
|
abnormal neuron differentiation
|
J:71181
|
Cdk5rap1tm1.2Tomik/Cdk5rap1tm1.2Tomik
(B6J.Cg-Cdk5rap1tm1.2Tomik)
|
abnormal cell physiology
|
J:220703
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:220703
|
abnormal mitochondrial crista morphology
|
J:220703
|
abnormal mitochondrial physiology
|
J:220703
|
abnormal mitophagy
|
J:220703
|
abnormal oxidative phosphorylation
|
J:220703
|
abnormal respiratory electron transport chain
|
J:220703
|
abnormal translation
|
J:220703
|
increased mitochondrial size
|
J:220703
|
increased skeletal muscle fiber mitochondrial DNA content
|
J:220703
|
oxidative stress
|
J:220703
|
Cdk5rap2an/Cdk5rap2an
(Not Specified)
|
decreased germ cell number
|
J:15165
|
decreased oocyte number
|
J:15165
|
Cdk5rap2an/Cdk5rap2an
(B6.Cg-Cdk5rap2an)
|
abnormal mitosis
|
J:160533
|
abnormal mitotic spindle morphology
|
J:160533
|
abnormal neuron proliferation
|
J:160533
|
increased neuron apoptosis
|
J:160533
|
Cdk5rap2an/Cdk5rap2an Tyrp1B-lt/Tyrp1B-lt
(WBB6F1)
|
abnormal mitosis
|
J:7537
|
aneuploidy
|
J:7537
|
Cdk5rap2em1Mama/Cdk5rap2em1Mama
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal male germ cell physiology
|
J:310617
|
cellular phenotype
|
J:310617
|
Cdk5rap2Gt(RRF465)Byg/Cdk5rap2Gt(RRF465)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:163849
|
abnormal centrosome morphology
|
J:163849
|
abnormal microtubule organizing center morphology
|
J:163849
|
abnormal mitosis
|
J:163849
|
abnormal mitotic spindle morphology
|
J:163849
|
abnormal pericentriolar material morphology
|
J:163849
|
abnormal plasma membrane morphology
|
J:163849
|
early cellular replicative senescence
|
J:163849
|
Cdk5rap2Gt(RRU031)Byg/Cdk5rap2Gt(RRU031)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal centrosome morphology
|
J:163849
|
abnormal pericentriolar material morphology
|
J:163849
|
cellular phenotype
|
J:163849
|
Cdk5rap3tm1b(EUCOMM)Hmgu/Cdk5rap3tm1b(EUCOMM)Hmgu
(involves: C57BL/6N * FVB/N)
|
decreased hepatocyte proliferation
|
J:272566
|
Cdk6tm1Bbd/Cdk6tm1Bbd
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
decreased T cell proliferation
|
J:92529
|
Cdk6tm1Phin/Cdk6tm1Phin
(involves: 129S4/SvJae)
|
decreased thymocyte apoptosis
|
J:144975
|
Cdk6tm3.1Phin/Cdk6tm3.1Phin
(involves: 129 * C57BL/6 * FVB/N)
|
increased T cell apoptosis
|
J:174697
|
Cdk7Gt(D032B11)1.1Wrst/Cdk7Gt(D032B11)1.1Wrst
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
absent fibroblast proliferation
|
J:183925
|
Cdk7Gt(D032B11)1.1Wrst/Cdk7Gt(D032B11)1.1Wrst Ndor1Tg(UBC-cre/ERT2)1Ejb/0
(involves: 129S/SvPas * 129S2/SvPas * C57BL/6 * SJL)
|
decreased telomere length
|
J:183925
|
Cdk7Gt(D032B11)Wrst/Cdk7Gt(D032B11)Wrst
(involves: 129S2/SvPas)
|
abnormal inner cell mass apoptosis
|
J:183925
|
increased embryonic tissue cell apoptosis
|
J:183925
|
Cdk8tm1a(EUCOMM)Hmgu/Cdk8tm1a(EUCOMM)Hmgu Tg(Ins2-cre)23Herr/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
increased cellular sensitivity to oxidative stress
|
J:281075
|
increased pancreatic beta cell apoptosis
|
J:281075
|
Cdk11btm1Vjk/Cdk11btm1Vjk
(involves: 129S6/SvEv * C57BL/6)
|
decreased cell proliferation
|
J:89908
|
increased embryonic tissue cell apoptosis
|
J:89908
|
Cdk12tm1.2Mjfn/Cdk12tm1.2Mjfn
(involves: FVB/N)
|
chromosomal instability
|
J:242195
|
increased apoptosis
|
J:242195
|
Cdk14tm1Dsp/Cdk14tm1Dsp
(involves: 129S/SvEvBrd * C57BL/6)
|
delayed axon extension
|
J:342122
|
Cdk16tm1.2Stge/Cdk16tm1.2Stge
(involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL)
|
abnormal germ cell morphology
|
J:183637
|
abnormal sperm annulus morphology
|
J:183637
|
abnormal sperm flagellum morphology
|
J:183637
|
abnormal sperm head morphology
|
J:183637
|
asthenozoospermia
|
J:183637
|
Cdk19em1Smoc/Cdk19em1Smoc
(C57BL/6JSmoc-Cdk19em1Smoc/Smoc)
|
decreased hematopoietic stem cell proliferation
|
J:322947
|
Cdk20tm1.1Jegg/Cdk20tm1.1Jegg
(involves: 129S7/SvEvBrd * FVB/N)
|
abnormal cilium morphology
|
J:243907
|
abnormal embryonic neuroepithelium primary cilium morphology
|
J:243907
|
abnormal primary cilium physiology
|
J:243907
|
Cdkal1tm1.2Tomik/Cdkal1tm1.2Tomik
(B6.Cg-Cdkal1tm1.2Tomik)
|
abnormal cell physiology
|
J:178248
|
Cdkn1atm1Led/Cdkn1atm1Led
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
abnormal cell cycle
|
J:28420
|
Cdkn1atm1Led/Cdkn1atm1Led
(involves: 129S6/SvEvTac)
|
abnormal cell cycle checkpoint function
|
J:57882
|
abnormal chromosome number
|
J:57882
|
increased fibroblast proliferation
|
J:57882
|
increased T cell proliferation
|
J:76041
|
Cdkn1atm1Led/Cdkn1atm1Led Gadd45atm1Ajf/Gadd45atm1Ajf
(either: (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6))
|
abnormal chromosome number
|
J:57882
|
increased fibroblast proliferation
|
J:57882
|
increased kidney cell proliferation
|
J:76041
|
increased mesangial cell number
|
J:76041
|
increased T cell proliferation
|
J:76041
|
mesangial cell interposition
|
J:76041
|
Cdkn1atm1Led/Cdkn1atm1Led Hdac2tm1.2Rdp/Hdac2tm1.2Rdp
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6)
|
abnormal mitosis
|
J:197818
|
early cellular replicative senescence
|
J:197818
|
Cdkn1atm1Led/Cdkn1atm1Led Hus1tm1Led/Hus1tm1Led
(involves: 129S6/SvEvTac)
|
chromosome breakage
|
J:63869
|
increased cellular sensitivity to hydroxyurea
|
J:63869
|
increased cellular sensitivity to ultraviolet irradiation
|
J:63869
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj
(involves: 129S2/SvPas)
|
abnormal neuronal precursor proliferation
|
J:90479
|
increased cell proliferation
|
J:180692
|
increased cellular sensitivity to ultraviolet irradiation
|
J:85569
|
increased DNA replication
|
J:59647
|
increased sensitivity to induced cell death
|
J:85569
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj
(B6;129S2-Cdkn1atm1Tyj/J)
|
impaired macrophage chemotaxis
|
J:108569
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:70894
|
increased T cell proliferation
|
J:60292
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj
(involves: 129/Sv * 129S2/SvPas * C57BL/6)
|
abnormal cell physiology
|
J:72780
|
delayed cellular replicative senescence
|
J:72780
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Cdkn1btm1Mlf/Cdkn1btm1Mlf
(involves: 129S2/SvPas * 129S4/SvJaeSor)
|
abnormal enterocyte proliferation
|
J:111081
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Cdkn2atm1Rdp/Cdkn2atm1Rdp
(involves: 129/Sv * 129S2/SvPas * C57BL/6 * C57BL/6J * SJL)
|
abnormal cell physiology
|
J:72780
|
delayed cellular replicative senescence
|
J:72780
|
increased keratinocyte proliferation
|
J:72780
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Cdkn2dtm1Maro/Cdkn2dtm1Maro
(involves: 129P2/OlaHsd * 129S2/SvPas * 129X1/SvJ * C57BL/6 * CD-1)
|
polyploidy
|
J:118337
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Csnk1a1tm1.1Ybn/Csnk1a1tm1.1Ybn Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129 * C57BL/6 * CD-1 * DBA/2)
|
abnormal enterocyte proliferation
|
J:204886
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Fahtm1Mgo/Fahtm1Mgo
(involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6)
|
increased hepatocyte apoptosis
|
J:138701
|
increased hepatocyte proliferation
|
J:138701
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Foxk1tm1Djg/Foxk1tm1Djg
(involves: 129S2/SvPas * 129S4/SvJae)
|
cellular phenotype
|
J:81688
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Gadd45atm1Ajf/Gadd45atm1Ajf
(either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ))
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:101710
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Mir34atm1.1Lhe/Mir34atm1.1Lhe
(involves: 129S2/SvPas * C57BL/6 * C57BL/6J)
|
abnormal cell physiology
|
J:180692
|
Cdkn1atm1Tyj/Cdkn1atm1Tyj Rb1tm1Tyj/Rb1tm1Tyj Tg(Rb1)1Blg/0
(involves: 129S2/SvPas)
|
polyploidy
|
J:65679
|
Cdkn1btm1Ako/Cdkn1btm1Ako
(involves: 129S1/Sv * C57BL)
|
abnormal fetal cardiomyocyte proliferation
|
J:57380
|
Cdkn1btm1Jro/Cdkn1btm1Jro
(involves: 129S4/SvJaeSor * C57BL/6)
|
decreased cell proliferation
|
J:71780
|
decreased keratinocyte proliferation
|
J:71780
|
decreased T cell proliferation
|
J:71780
|
Cdkn1btm1Kin/Cdkn1btm1Kin Zfp949tm1Htno/Zfp949tm1Htno
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:259302
|
Cdkn1btm1Mlf/Cdkn1btm1Mlf
(involves: 129S4/SvJaeSor * C57BL/6J)
|
increased T cell proliferation
|
J:33400
|
Cdkn1btm1Mlf/Cdkn1btm1Mlf
(involves: 129S4/SvJaeSor)
|
abnormal neuron differentiation
|
J:109091
|
impaired neuronal migration
|
J:109091
|
Cdkn1btm1Mlf/Cdkn1btm1Mlf
(involves: 129S4/SvJaeSor * C57BL/6NHsd)
|
abnormal cell proliferation
|
J:53290
|
Cdkn1btm1Mlf/Cdkn1btm1Mlf Cdkn2dtm1Maro/Cdkn2dtm1Maro
(involves: 129X1/SvJ * C57BL/6)
|
abnormal mitosis
|
J:58522
|
increased cell proliferation
|
J:58522
|
increased mitotic index
|
J:58522
|
increased neuron apoptosis
|
J:58522
|
Cdkn1btm1Mlf/Cdkn1btm1Mlf Myctm1Atp/Myc+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * FVB/N)
|
decreased T cell proliferation
|
J:73369
|
Cdkn1btm1Mlf/Cdkn1btm1Mlf Rbx1Gt(XB674)Byg/Rbx1Gt(XB674)Byg
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
cellular phenotype
|
J:147759
|
Cdkn1ctm1.1(Cdkn1b*)Kei/Cdkn1c+
(involves: 129P2/OlaHsd * C57BL/6J)
|
paternal imprinting
|
J:147145
|
Cdkn1ctm1Bbd/Cdkn1c+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
paternal imprinting
|
J:40142
|
Cdkn1ctm1Bbd/Cdkn1ctm1Bbd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased midbrain apoptosis
|
J:88146
|
Cdkn1ctm1Kat/Cdkn1c+
(involves: 129P2/OlaHsd * C57BL/6)
|
paternal imprinting
|
J:61190
|
Cdkn1ctm1Kat/Cdkn1c+
(involves: 129P2/OlaHsd * C57BL/6J)
|
paternal imprinting
|
J:147145
|
Cdkn1ctm1Sje/Cdkn1c+
(involves: 129S7/SvEvBrd * C57BL/6)
|
paternal imprinting
|
J:40203
|
Cdkn1ctm1Sje/Cdkn1c+ Kcnq1ot1tm1Tilg/Kcnq1ot1+
(involves: 129 * C57BL/6)
|
abnormal imprinting
|
J:108700
|
Cdkn1ctm1Sje/Cdkn1ctm1Sje
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased lens epithelium apoptosis
|
J:40203
|
Cdkn2aem2Cjs/Cdkn2aem2Cjs
(C57BL/6-Cdkn2aem2Cjs)
|
abnormal spermatocyte morphology
|
J:244260
|
oligozoospermia
|
J:244260
|
Cdkn2atm1Cjs/Cdkn2atm1Cjs
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:44427
|
abnormal spermatocyte morphology
|
J:244260
|
increased fibroblast proliferation
|
J:44427
|
oligozoospermia
|
J:244260
|
Cdkn2atm1Cjs/Cdkn2atm1Cjs
(involves: 129X1/SvJ)
|
oligozoospermia
|
J:147752
|
Cdkn2atm1Cjs/Cdkn2atm1Cjs Gt(ROSA)26Sortm1.1(MYC/ERT2)Gev/Gt(ROSA)26Sortm1.1(MYC/ERT2)Gev
(involves: 129X1/SvJ * C57BL/6 * FVB/N)
|
increased cell proliferation
|
J:142030
|
Cdkn2atm1Cjs/Cdkn2atm1Cjs Tacstd2tm1Lsm/Tacstd2tm1Lsm
(involves: 129X1/SvJ * C57BL/6)
|
increased keratinocyte migration
|
J:182647
|
increased keratinocyte proliferation
|
J:182647
|
Cdkn2atm1Nesh/Cdkn2atm1Nesh
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal cell physiology
|
J:88365
|
Cdkn2atm1Rdp/Cdkn2a+ Lig4tm1Fwa/Lig4tm1Fwa
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL)
|
decreased cell proliferation
|
J:63078
|
increased cellular sensitivity to ionizing radiation
|
J:63078
|
increased neuron apoptosis
|
J:63078
|
Cdkn2atm1Rdp/Cdkn2atm1Rdp
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal cell cycle
|
J:53805
|
increased fibroblast proliferation
|
J:53805
|
Cdkn2atm1Rdp/Cdkn2atm1Rdp
(involves: 129/Sv * C57BL/6J * FVB/N * SJL)
|
abnormal cell physiology
|
J:88365
|
Cdkn2atm1Rdp/Cdkn2atm1Rdp
(involves: 129/Sv * C57BL/6 * C57BL/6J * SJL)
|
abnormal cell physiology
|
J:72780
|
delayed cellular replicative senescence
|
J:72780
|
Cdkn2atm1Rdp/Cdkn2atm1Rdp Dicer1tm1Snj/Dicer1tm1Snj
(involves: 129/Sv * 129S7/SvEvBrd * C57BL/6 * SJL)
|
increased cell proliferation
|
J:139257
|
Cdkn2atm1Rdp/Cdkn2atm1Rdp Dicer1tm1Snj/Dicer1tm1Snj
(involves: 129/Sv * 129S7/SvEvBrd * C57BL/6 * SJL)
|
cellular phenotype
|
J:139257
|
Cdkn2atm1Rdp/Cdkn2atm1Rdp Lig4tm1Fwa/Lig4tm1Fwa
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6J * SJL)
|
decreased cell proliferation
|
J:63078
|
Cdkn2atm1Rdp/Cdkn2atm1Rdp Terctm1Rdp/Terctm1Rdp
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal telomere length
|
J:120065
|
decreased cell proliferation
|
J:120065
|
increased male germ cell apoptosis
|
J:120065
|
Cdkn2atm2.1Brn/Cdkn2atm2.1Brn Hdac2tm1.2Rdp/Hdac2tm1.2Rdp
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
abnormal mitosis
|
J:197818
|
Cdkn2atm2.1Nesh/Cdkn2atm2.1Nesh Nrastm1.1Nesh/Nrastm1.1Nesh Tg(Tyr-cre/ERT2)13Bos/0
(B6J.Cg-Tg(Tyr-cre/ERT2)13Bos Nrastm1.1Nesh Cdkn2atm2.1Nesh)
|
abnormal melanocyte proliferation
|
J:220627
|
Cdkn2atm2.1Nesh/Cdkn2atm2.1Nesh Nrastm1Tyj/Nrastm1Tyj Tg(Tyr-cre/ERT2)13Bos/0
(B6J.Cg-Tg(Tyr-cre/ERT2)13Bos Nrastm1Tyj Cdkn2atm2.1Nesh)
|
abnormal melanocyte proliferation
|
J:220627
|
Cdkn2atm2.1Rdp/Cdkn2atm2.1Rdp
(involves: 129S6/SvEvTac * FVB/N)
|
increased splenocyte proliferation
|
J:71394
|
Cdkn2atm2Brn/Cdkn2atm2Brn Krastm4Tyj/Kras+ Tg(Pdx1-cre)6Tuv/0
(involves: 129P2/OlaHsd * 129S4/SvJae * FVB/N)
|
increased cell proliferation
|
J:195229
|
Cdkn2btm1Bbd/Cdkn2btm1Bbd
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell physiology
|
J:63299
|
increased fibroblast proliferation
|
J:63299
|
Cdkn2btm1Bbd/Cdkn2btm1Bbd Cdkn2ctm1Bbd/Cdkn2ctm1Bbd
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell physiology
|
J:63299
|
increased fibroblast proliferation
|
J:63299
|
Cdkn2ctm1Bbd/Cdkn2ctm1Bbd
(involves: 129S1/Sv * C57BL/6)
|
abnormal apoptosis
|
J:68829
|
abnormal neuron differentiation
|
J:102702
|
abnormal neuronal migration
|
J:102702
|
Cdkn2ctm1Bbd/Cdkn2ctm1Bbd Cdkn2dtm1Maro/Cdkn2dtm1Maro
(involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6)
|
abnormal germ cell morphology
|
J:68829
|
abnormal male meiosis
|
J:68829
|
asthenozoospermia
|
J:68829
|
decreased germ cell number
|
J:68829
|
oligozoospermia
|
J:68829
|
Cdkn2ctm1Bbd/Cdkn2ctm1Bbd Ptch1tm1Mps/Ptch1+
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:102702
|
Cdkn2ctm1Bbd/Cdkn2ctm1Bbd Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S1/Sv * 129S2/SvPas * C57BL/6)
|
abnormal neuron differentiation
|
J:102702
|
Cdkn2dtm1Maro/Cdkn2dtm1Maro
(involves: 129P2/OlaHsd * C57BL/6)
|
increased male germ cell apoptosis
|
J:58959
|
multinucleated giant male germ cells
|
J:58959
|
Cdkn2dtm1Maro/Cdkn2dtm1Maro
(involves: 129X1/SvJ * C57BL/6)
|
abnormal apoptosis
|
J:68829
|
abnormal male meiosis
|
J:68829
|
oligozoospermia
|
J:68829
|
Cdnftm1.1Uhb/Cdnftm1.1Uhb
(either: B6JRcc.129P2(Cg)-Cdnftm1.1Uhb or (involves: 129P2/OlaHsd * C57BL/6JRcc * ICR))
|
enhanced autophagy
|
J:285339
|
Cdontm1Rsk/Cdontm1Rsk
(B6.129-Cdontm1Rsk)
|
abnormal neuronal precursor proliferation
|
J:109070
|
Cdontm2Rsk/Cdontm2Rsk
(B6.129-Cdontm2Rsk)
|
abnormal neuronal precursor proliferation
|
J:109070
|
Cdx1tm1Pgr/Cdx1tm1Pgr Gt(ROSA)26Sortm1(en/Cdx1,-EGFP)Npln/Gt(ROSA)26Sor+ Tg(Pax3-cre)1Joe/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal melanoblast migration
|
J:231654
|
Cdx2tm1Fbe/Cdx2tm1Fbe
(involves: ICR)
|
abnormal inner cell mass apoptosis
|
J:98502
|
increased trophectoderm apoptosis
|
J:98502
|
Cdx2tm1Khk/Cdx2tm1Khk Tg(Foxa3-cre)1Khk/0
(involves: C57BL/6 * DBA * SJL)
|
abnormal intestinal goblet cell morphology
|
J:149479
|
Cdx2tm1Mmt/Cdx2+
(B6.129X1-Cdx2tm1Mmt)
|
abnormal cell cycle checkpoint function
|
J:86737
|
abnormal chromosome morphology
|
J:86737
|
decreased apoptosis
|
J:86737
|
increased apoptosis
|
J:86737
|
Cdx2tm1Mmt/Cdx2+ Apctm1Mmt/Apc+
(B6.129-Cdx2tm1Mmt Apctm1Mmt)
|
abnormal cell cycle checkpoint function
|
J:86737
|
abnormal chromosome morphology
|
J:86737
|
decreased apoptosis
|
J:86737
|
increased apoptosis
|
J:86737
|
Cdx2tm1Mmt/Cdx2tm1Mmt
(involves: 129X1/SvJ * C57BL/6)
|
absent inner cell mass proliferation
|
J:47050
|
Cdx2tm2Fbe/Cdx2tm2Fbe Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell migration
|
J:179732
|
Cdx2tm2Fbe/Cdx2tm2Fbe Tg(Cyp1a1-cre/ERT)1Dwi/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal cell migration
|
J:179732
|
Cdyltm1.1Yuw/Cdyltm1.1Yuw Emx1tm1(cre)Yql/Emx1+
(involves: 129S2/SvPas * C57BL/6)
|
abnormal neuronal migration
|
J:251551
|
Ceacam1tm1Rsb/Ceacam1tm1Rsb Tg(Lck-cre)1Cwi/0
(involves: 129)
|
increased T cell proliferation
|
J:116136
|
Ceacam2tm1Snaj/Ceacam2tm1Snaj
(involves: 129S4/SvJae * C57BL/6)
|
decreased fatty acid oxidation
|
J:181979
|
decreased skeletal muscle cell glucose uptake
|
J:181979
|
Cebpatm1Gonz/Cebpatm1Gonz Cebpbtm1Es/Cebpbtm1Es Tg(KRT14-cre/ERT)20Efu/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
|
abnormal keratinocyte differentiation
|
J:158721
|
increased keratinocyte proliferation
|
J:158721
|
Cebpatm1Gonz/Cebpatm1Gonz Cebpbtm1Nerl/Cebpbtm1Nerl Tg(KRT14-cre)1Cgn/0
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased keratinocyte proliferation
|
J:154022
|
Cebpatm1Gonz/Cebpatm1Gonz Tg(KRT14-cre/ERT)20Efu/0
(involves: 129X1/SvJ * C57BL/6 * CD-1)
|
increased keratinocyte proliferation
|
J:158721
|
Cebpatm1Gonz/Cebpatm2Nerl Cebpbtm1Nerl/Cebpbtm1Nerl Tg(KRT14-cre)1Cgn/0
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased keratinocyte proliferation
|
J:154022
|
Cebpatm1Gonz/Cebpatm9Nerl Cebpbtm1Nerl/Cebpbtm1Nerl Tg(KRT14-cre)1Cgn/0
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased keratinocyte proliferation
|
J:154022
|
Cebpatm1Timc/Cebpatm1Timc
(Not Specified)
|
decreased hepatocyte proliferation
|
J:163725
|
Cebpatm6Nerl/Cebpatm6Nerl
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased adipocyte glucose uptake
|
J:120098
|
decreased skeletal muscle cell glucose uptake
|
J:120098
|
Cebpbtm1.1Acle/Cebpbtm1.1Acle
(involves: 129P2/OlaHsd * BALB/c * C57BL/6)
|
abnormal osteoblast physiology
|
J:150006
|
abnormal osteoclast differentiation
|
J:150006
|
enhanced osteoblast differentiation
|
J:150006
|
Cebpbtm1.1Maka/Cebpbtm1.1Maka Ins2Akita/Ins2Akita Tg(Ins2-cre)23Herr/0
(involves: 129P2/OlaHsd * C57BL/6J * C57BL/6NSlc * CBA/J)
|
abnormal pancreatic islet cell apoptosis
|
J:156725
|
Cebpbtm1.1Maka/Cebpbtm1.1Maka Leprdb/Leprdb Tg(Ins2-cre)23Herr/0
(involves: 129P2/OlaHsd * C57BL/6J * C57BLKS/J * CBA/J)
|
abnormal pancreatic islet cell apoptosis
|
J:156725
|
Cebpbtm1Es/Cebpbtm1Es Tg(KRT5-cre)5132Jlj/?
(involves: 129S1/Sv * C57BL/6J * DBA/2J)
|
increased keratinocyte apoptosis
|
J:107334
|
Cebpbtm1Es/Cebpbtm1Es Tg(KRT14-cre/ERT)20Efu/0
(involves: 129S1/Sv * C57BL/6 * CD-1)
|
abnormal keratinocyte differentiation
|
J:158721
|
increased keratinocyte proliferation
|
J:158721
|
Cebpbtm1Kish/Cebpbtm1Kish
(involves: 129P2/OlaHsd)
|
abnormal cell differentiation
|
J:45062
|
impaired macrophage phagocytosis
|
J:77003
|
Cebpbtm1Kish/Cebpbtm1Kish Cebpdtm1Aki/Cebpdtm1Aki
(involves: 129P2/OlaHsd)
|
abnormal cell differentiation
|
J:45062
|
Cebpbtm1Pfj/Cebpbtm1Pfj
(involves: 129S1/Sv * C57BL/6)
|
abnormal osteoblast physiology
|
J:150006
|
abnormal osteoclast differentiation
|
J:150006
|
impaired granulosa cell differentiation
|
J:43075
|
Cebpbtm1Pfj/Cebpbtm1Pfj
(B6.Cg-Cebpbtm1Pfj)
|
increased keratinocyte apoptosis
|
J:73558
|
Cebpbtm1Vpo/Cebpbtm1Vpo
(involves: 129S/SvEv * MF1)
|
increased mesangial cell number
|
J:25215
|
increased skeletal muscle cell glucose uptake
|
J:62132
|
Cebpbtm1Vpo/Cebpbtm1Vpo
(FVB.129S-Cebpbtm1Vpo)
|
decreased sensitivity to induced cell death
|
J:52729
|
Cebpbtm2.1Acle/Cebpbtm2.1Acle
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6)
|
decreased cell proliferation
|
J:155795
|
Cebpdtm1Aki/Cebpdtm1Aki
(involves: 129P2/OlaHsd)
|
abnormal cell differentiation
|
J:45062
|
Cebpdtm1Pfj/Cebpdtm1Pfj
(involves: 129S1/Sv)
|
increased mammary gland epithelial cell proliferation
|
J:103094
|
Cebpetm1Kgx/Cebpetm1Kgx
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
abnormal eosinophil differentiation
|
J:76024
|
abnormal granulocyte differentiation
|
J:76024
|
abnormal neutrophil differentiation
|
J:76024
|
Cebpetm1Kgx/Cebpetm1Kgx
(involves: 129S6/SvEvTac)
|
abnormal eosinophil differentiation
|
J:76024
|
abnormal granulocyte differentiation
|
J:76024
|
abnormal neutrophil differentiation
|
J:76024
|
Celf2tm1.1Yjin/Celf2tm1.1Yjin
(involves: BALB/c * C57BL/6 * FVB/N)
|
abnormal axon extension
|
J:269731
|
Celf3tm1Ade/Celf3tm1Ade
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal sperm motility
|
J:128362
|
oligozoospermia
|
J:128362
|
Celsr1Crsh/Celsr1Crsh
(involves: 101/H * BALB/c * C3H/HeH)
|
abnormal outer hair cell kinocilium location or orientation
|
J:84285
|
Celsr1Scy/Celsr1Scy
(involves: BALB/cAnN * C3H/He * C3H/HeH)
|
abnormal outer hair cell kinocilium location or orientation
|
J:84285
|
Celsr3tm1Agof/Celsr3tm1Agof
(either: CD-1.129P2-Celsr3tm1Agof or (involves: 129P2/OlaHsd * C57BL/6 * CD-1))
|
abnormal axon guidance
|
J:98367
|
Celsr3tm1Mrc/Celsr3tm1Mrc
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S6/SvEvTac * C57BL/6NCr))
|
impaired neuronal migration
|
J:149145
|
Cend1tm1.1Rmat/Cend1tm1.1Rmat
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6)
|
abnormal cerebellar granule cell migration
|
J:164148
|
abnormal neuron proliferation
|
J:164148
|
Cenpatm1Khac/Cenpatm1Khac
(involves: 129 * C57BL/6)
|
abnormal mitosis
|
J:60186
|
Cenpatm2Khac/Cenpatm2Khac
(involves: 129S1/Sv * C57BL/6)
|
abnormal apoptosis
|
J:84634
|
abnormal cell nucleus morphology
|
J:84634
|
abnormal chromosome morphology
|
J:84634
|
aneuploidy
|
J:84634
|
Cenpbtm1Gmay/Cenpbtm1Gmay
(involves: 129S7/SvEvBrd)
|
cellular phenotype
|
J:53053
|
Cenpbtm1Khac/Cenpbtm1Khac
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
oligozoospermia
|
J:47171
|
Cenpbtm1Khac/Cenpbtm2Khac
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
cellular phenotype
|
J:47171
|
Cenpc1tm1Khac/Cenpc1tm1Khac
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell nucleus morphology
|
J:45656
|
abnormal chromosome morphology
|
J:45656
|
abnormal mitosis
|
J:45656
|
Cenpetm1Dwc/Cenpetm1Dwc
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal inner cell mass proliferation
|
J:81046
|
abnormal mitosis
|
J:81046
|
Cenpetm1Dwc/Cenpetm2Dwc
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal mitosis
|
J:81046
|
Cenpetm2Dwc/Cenpetm2Dwc
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal mitosis
|
J:81046
|
chromosomal instability
|
J:81046
|
Cenpftm1Dbdr/Cenpftm1Dbdr Tg(Tnnt2-cre)5Blh/0
(involves: C57BL/6 * DBA/2 * ICR)
|
decreased fetal cardiomyocyte proliferation
|
J:185133
|
Cenpvtm1c(EUCOMM)Hmgu/Cenpvtm1c(EUCOMM)Hmgu Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6N * FVB)
|
abnormal female meiosis
|
J:314905
|
Cenpvtm1c(EUCOMM)Hmgu/Cenpvtm1c(EUCOMM)Hmgu Tg(Spo11-cre)1Rsw/0
(involves: C57BL/6N)
|
impaired polar body extrusion
|
J:314905
|
Cenpvtm1c(EUCOMM)Hmgu/Cenpvtm1c(EUCOMM)Hmgu Tg(Stra8-icre)1Reb/0
(involves: C57BL/6N * FVB/NJ)
|
impaired polar body extrusion
|
J:314905
|
Cenpvtm1d(EUCOMM)Hmgu/Cenpvtm1d(EUCOMM)Hmgu
(involves: C57BL/6N)
|
abnormal female meiosis
|
J:314905
|
abnormal meiotic spindle morphology
|
J:314905
|
impaired polar body extrusion
|
J:314905
|
Cep20tm1.1(KOMP)Vlcg/Cep20tm1.1(KOMP)Vlcg
(B6(Cg)-Cep20tm1.1(KOMP)Vlcg)
|
absent embryonic cilia
|
J:308526
|
Cep55em1.1Hyli/Cep55em1.1Hyli
(involves: C57BL/6)
|
abnormal cell cycle
|
J:313163
|
abnormal embryonic neuroepithelium primary cilium morphology
|
J:313163
|
abnormal primary cilium morphology
|
J:313163
|
decreased cell proliferation
|
J:313163
|
increased brain ependyma motile cilium length
|
J:313163
|
increased kidney epithelial cell primary cilium length
|
J:313163
|
Cep55tm1a(EUCOMM)Hmgu/Cep55tm1a(EUCOMM)Hmgu
(involves: C57BL/6N)
|
abnormal mitotic cytokinesis
|
J:287102
|
increased cell nucleus count
|
J:287102
|
increased neuron apoptosis
|
J:287102
|
Cep55tm1c(EUCOMM)Hmgu/Cep55tm1c(EUCOMM)Hmgu Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: C57BL/6N * C57BL/6NTac)
|
increased cell nucleus count
|
J:287102
|
Cep57em1Jvd/Cep57+
(involves: 129 * C57BL/6)
|
abnormal cell morphology
|
J:264300
|
aneuploidy
|
J:264300
|
Cep57em1Jvd/Cep57em1Jvd
(involves: 129 * C57BL/6)
|
abnormal cell morphology
|
J:264300
|
abnormal mitotic spindle morphology
|
J:264300
|
aneuploidy
|
J:264300
|
Cep57em1Jvd/Cep57em2Jvd
(involves: 129 * C57BL/6 * FVB/N)
|
abnormal cell morphology
|
J:264300
|
Cep57em2Jvd/Cep57+
(involves: FVB/N)
|
aneuploidy
|
J:264300
|
Cep63Gt(EUCE0251h11)Hmgu/Cep63Gt(EUCE0251h11)Hmgu
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:224364
|
abnormal male meiosis
|
J:224364
|
abnormal mitosis
|
J:224364
|
abnormal mitotic spindle morphology
|
J:224364
|
abnormal spermatocyte morphology
|
J:224364
|
abnormal spermatogonia morphology
|
J:224364
|
abnormal synaptonemal complex
|
J:224364
|
abnormal telomere morphology
|
J:224364
|
azoospermia
|
J:224364
|
decreased oocyte number
|
J:224364
|
decreased spermatid number
|
J:224364
|
increased forebrain apoptosis
|
J:224364
|
increased testis apoptosis
|
J:224364
|
polyploidy
|
J:224364
|
Cep70em1Qiao/Cep70em1Qiao
(C57BL/6J-Cep70em1Qiao)
|
abnormal acrosome morphology
|
J:333258
|
azoospermia
|
J:333258
|
coiled sperm flagellum
|
J:333258
|
increased male germ cell apoptosis
|
J:333258
|
kinked sperm flagellum
|
J:333258
|
short sperm flagellum
|
J:333258
|
small sperm head
|
J:333258
|
teratozoospermia
|
J:333258
|
Cep72em1Lmgg/Cep72em1Lmgg
(C57BL/6N-Cep72em1Lmgg)
|
abnormal outer dense fiber morphology
|
J:330932
|
abnormal sperm axoneme morphology
|
J:330932
|
abnormal sperm flagellum morphology
|
J:330932
|
abnormal sperm head morphology
|
J:330932
|
abnormal sperm nucleus morphology
|
J:330932
|
abnormal sperm principal piece morphology
|
J:330932
|
absent acrosome
|
J:330932
|
absent sperm head
|
J:330932
|
coiled sperm flagellum
|
J:330932
|
teratozoospermia
|
J:330932
|
Cep78em1Xjg/Cep78em1Xjg
(C57BL/6J-Cep78em1Xjg)
|
abnormal acrosome assembly
|
J:336106
|
abnormal manchette assembly
|
J:336106
|
abnormal manchette perinuclear ring morphology
|
J:336106
|
abnormal outer dense fiber morphology
|
J:336106
|
abnormal photoreceptor connecting cilium morphology
|
J:336106
|
abnormal sperm axoneme morphology
|
J:336106
|
abnormal sperm connecting piece morphology
|
J:336106
|
abnormal sperm flagellum morphology
|
J:336106
|
abnormal sperm head morphology
|
J:336106
|
abnormal sperm mitochondrial sheath morphology
|
J:336106
|
absent sperm flagellum
|
J:336106
|
asthenozoospermia
|
J:336106
|
coiled sperm flagellum
|
J:336106
|
decreased sperm progressive motility
|
J:336106
|
detached acrosome
|
J:336106
|
elongated manchette
|
J:336106
|
multiflagellated sperm
|
J:336106
|
oligozoospermia
|
J:336106
|
short sperm flagellum
|
J:336106
|
teratozoospermia
|
J:336106
|
Cep78em2Gpt/Cep78em2Gpt
(C57BL/6JGpt-Cep78em2Gpt)
|
abnormal sperm axoneme morphology
|
J:333155
|
abnormal sperm flagellum morphology
|
J:333155
|
abnormal sperm head morphology
|
J:333155
|
abnormal sperm midpiece morphology
|
J:333155
|
absent sperm flagellum
|
J:333155
|
asthenozoospermia
|
J:333155
|
oligozoospermia
|
J:333155
|
short sperm flagellum
|
J:333155
|
teratozoospermia
|
J:333155
|
Cep120tm1.1Blnw/Cep120tm1.2Blnw Tg(Nes-cre)1Atp/0
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N)
|
abnormal cell morphology
|
J:220629
|
abnormal cilium morphology
|
J:220629
|
absent brain ependyma motile cilia
|
J:220629
|
decreased cerebellar granule cell precursor proliferation
|
J:220629
|
Cep120tm1.2Blnw/Cep120tm1.2Blnw
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell morphology
|
J:220629
|
abnormal cilium morphology
|
J:220629
|
Cep128em1Fzh/Cep128em1Fzh
(C57BL/6-Cep128em1Fzh)
|
abnormal sperm axoneme morphology
|
J:323071
|
abnormal sperm flagellum morphology
|
J:323071
|
asthenozoospermia
|
J:323071
|
decreased sperm progressive motility
|
J:323071
|
oligozoospermia
|
J:323071
|
teratozoospermia
|
J:323071
|
Cep128em2Fzh/Cep128em2Fzh
(C57BL/6-Cep128em2Fzh)
|
abnormal sperm axoneme morphology
|
J:323071
|
abnormal sperm flagellum morphology
|
J:323071
|
asthenozoospermia
|
J:323071
|
decreased sperm progressive motility
|
J:323071
|
oligozoospermia
|
J:323071
|
teratozoospermia
|
J:323071
|
Cep128em3Fzh/Cep128em3Fzh
(C57BL/6-Cep128em3Fzh)
|
abnormal sperm axoneme morphology
|
J:323071
|
asthenozoospermia
|
J:323071
|
hairpin sperm flagellum
|
J:323071
|
oligozoospermia
|
J:323071
|
teratozoospermia
|
J:323071
|
Cep131Gt(CC0635)Wtsi/Cep131Gt(CC0635)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal sperm axoneme morphology
|
J:223125
|
abnormal sperm connecting piece morphology
|
J:223125
|
abnormal sperm flagellum morphology
|
J:223125
|
abnormal sperm nucleus morphology
|
J:223125
|
cellular phenotype
|
J:223125
|
detached acrosome
|
J:223125
|
increased male germ cell apoptosis
|
J:223125
|
oligozoospermia
|
J:223125
|
short sperm flagellum
|
J:223125
|
teratozoospermia
|
J:223125
|
Cep135em1Mama/Cep135em1Mama
(involves: C57BL/6 * C57BL/6J * CBA)
|
cellular phenotype
|
J:310617
|
Cep135em2Mama/Cep135em2Mama
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal cell cycle
|
J:310617
|
abnormal cell nucleus morphology
|
J:310617
|
abnormal centrosome morphology
|
J:310617
|
abnormal mitosis
|
J:310617
|
abnormal mitotic spindle morphology
|
J:310617
|
aneuploidy
|
J:310617
|
chromosomal instability
|
J:310617
|
decreased cell proliferation
|
J:310617
|
increased embryonic tissue cell apoptosis
|
J:310617
|
Cep135em2Mama/Cep135em2Mama Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6 * C57BL/6J * CBA)
|
abnormal mitosis
|
J:310617
|
Cep152tm1a(EUCOMM)Wtsi/Cep152tm1a(EUCOMM)Wtsi
(involves: C57BL/6N * FVB/NJ)
|
abnormal centrosome morphology
|
J:208632
|
decreased embryonic neuroepithelium primary cilium number
|
J:208632
|
increased apoptosis
|
J:208632
|
Cep164tm1a(EUCOMM)Wtsi/Cep164tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal primary cilium morphology
|
J:255142
|
decreased embryonic neuroepithelium primary cilium number
|
J:255142
|
Cep164tm1c(EUCOMM)Wtsi/Cep164tm1c(EUCOMM)Wtsi Tg(FOXJ1-cre)F26Htzm/0
(involves: C3H * C57BL/6 * C57BL/6J * C57BL/6N)
|
abnormal brain ependyma motile cilium location or orientation
|
J:255142
|
abnormal olfactory epithelium cilium morphology
|
J:255142
|
abnormal oviduct epithelium motile cilium morphology
|
J:255142
|
abnormal respiratory motile cilium morphology
|
J:255142
|
abnormal sperm flagellum morphology
|
J:307614
|
absent sperm head
|
J:307614
|
azoospermia
|
J:255142
|
decreased brain ependyma motile cilium number
|
J:255142
|
decreased male germ cell number
|
J:255142
|
decreased respiratory motile cilia number
|
J:255142
|
oligozoospermia
|
J:307614
|
teratozoospermia
|
J:307614
|
Cep250em1Glvr/Cep250em1Glvr
(C57BL/6-Cep250em1Glvr)
|
abnormal centrosome morphology
|
J:324876
|
arrest of male meiosis
|
J:324876
|
azoospermia
|
J:324876
|
increased male germ cell apoptosis
|
J:324876
|
Cep250tm1a(EUCOMM)Wtsi/Cep250tm1a(EUCOMM)Wtsi Tg(Stra8-icre)1Reb/0
(involves: C57BL/6N)
|
decreased male germ cell number
|
J:326549
|
Cep250tm1b(EUCOMM)Wtsi/Cep250tm1b(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal centrosome morphology
|
J:326549
|
abnormal male meiosis
|
J:326549
|
azoospermia
|
J:326549
|
decreased male germ cell number
|
J:326549
|
decreased oocyte number
|
J:326549
|
Cep290Gt(CC0582)Wtsi/Cep290Gt(CC0582)Wtsi
(129P2/OlaHsd-Cep290Gt(CC0582)Wtsi)
|
abnormal cell nucleus morphology
|
J:226246
|
abnormal DNA replication
|
J:226246
|
abnormal double-strand DNA break repair
|
J:226246
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:212182
|
absent kidney epithelial cell primary cilium
|
J:226246
|
Cep290rd16/Cep290rd16
(involves: BXD24/TyJ)
|
abnormal cilium morphology
|
J:204004
|
Cept1tm1.1Sem/Cept1tm1.1Sem Tg(ACTA1-cre)79Jme/0
(involves: C57BL/6J * SJL)
|
abnormal cellular respiration
|
J:249456
|
cellular phenotype
|
J:249456
|
Cerkltm1.1Geno/Cerkltm1.1Geno
(involves: 129 * C57BL/6J)
|
increased retina apoptosis
|
J:185135
|
Cers1tm1.1Kwi/Cers1tm1.1Kwi
(involves: 129P2/OlaHsd * C57BL/6)
|
increased neuron apoptosis
|
J:193419
|
Cers6tm1.1Arte/Cers6tm1.1Arte
(involves: BALB/cJ * C57BL/6N)
|
abnormal cellular respiration
|
J:215519
|
increased fatty acid oxidation
|
J:215519
|
Cert1Gt(RRF047)Byg/Cert1Gt(RRF047)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:146172
|
abnormal endoplasmic reticulum morphology
|
J:146172
|
abnormal mitochondrial morphology
|
J:146172
|
abnormal mitochondrial physiology
|
J:146172
|
cellular phenotype
|
J:146172
|
decreased cell proliferation
|
J:146172
|
Ces5aem1Zuk/Ces5aem1Zuk
(involves: C57BL/6 * DBA/2)
|
asthenozoospermia
|
J:295177
|
decreased sperm progressive motility
|
J:295177
|
oligozoospermia
|
J:295177
|
Cetn1tm1.1Wbae/Cetn1tm1.1Wbae
(Not Specified)
|
abnormal acrosome assembly
|
J:276829
|
abnormal microtubule organizing center morphology
|
J:276829
|
abnormal sperm axoneme morphology
|
J:276829
|
abnormal sperm flagellum morphology
|
J:276829
|
abnormal sperm head morphology
|
J:276829
|
abnormal sperm midpiece morphology
|
J:276829
|
abnormal sperm nucleus morphology
|
J:276829
|
abnormal spermatid morphology
|
J:276829
|
absent sperm flagellum
|
J:276829
|
immotile sperm
|
J:276829
|
oligozoospermia
|
J:276829
|
short sperm flagellum
|
J:276829
|
teratozoospermia
|
J:276829
|
Cetn2tm1.1Wbae/Y
(involves: 129 * FVB/N)
|
abnormal brain ependyma motile cilium location or orientation
|
J:211061
|
abnormal olfactory epithelium cilium morphology
|
J:211061
|
cellular phenotype
|
J:211061
|
Cetn2tm1.1Wbae/Y Cetn3tm1a(EUCOMM)Wtsi/Cetn3tm1a(EUCOMM)Wtsi
(involves: 129 * C57BL/6J * C57BL/6N * FVB/N)
|
abnormal photoreceptor connecting cilium morphology
|
J:275959
|
Cfap43em1Fzh/Cfap43em1Fzh
(involves: C57BL/6)
|
abnormal outer dense fiber morphology
|
J:258613
|
abnormal sperm axoneme morphology
|
J:258613
|
abnormal sperm flagellum morphology
|
J:258613
|
abnormal sperm flagellum thickness
|
J:258613
|
absent sperm axonemal central pair
|
J:258613
|
absent sperm flagellum
|
J:258613
|
asthenozoospermia
|
J:258613
|
coiled sperm flagellum
|
J:258613
|
kinked sperm flagellum
|
J:258613
|
oligozoospermia
|
J:258613
|
short sperm flagellum
|
J:258613
|
Cfap43em1Pfr/Cfap43+
(involves: C57BL/6J)
|
decreased sperm progressive motility
|
J:257803
|
Cfap43em1Pfr/Cfap43em1Pfr
(involves: C57BL/6J)
|
abnormal sperm axoneme morphology
|
J:257803
|
abnormal sperm flagellum morphology
|
J:257803
|
abnormal sperm head morphology
|
J:257803
|
abnormal sperm radial spoke morphology
|
J:257803
|
absent sperm axonemal central pair
|
J:257803
|
coiled sperm flagellum
|
J:257803
|
immotile sperm
|
J:257803
|
short sperm flagellum
|
J:257803
|
teratozoospermia
|
J:257803
|
thick sperm flagellum
|
J:257803
|
Cfap43em1Sono/Cfap43em1Sono
(Not Specified)
|
abnormal motile cilium morphology
|
J:285551
|
abnormal respiratory motile cilium morphology
|
J:285551
|
abnormal sperm flagellum morphology
|
J:285551
|
Cfap43em2Fzh/Cfap43em2Fzh
(involves: C57BL/6)
|
abnormal outer dense fiber morphology
|
J:258613
|
abnormal sperm axoneme morphology
|
J:258613
|
abnormal sperm flagellum morphology
|
J:258613
|
abnormal sperm flagellum thickness
|
J:258613
|
absent sperm axonemal central pair
|
J:258613
|
absent sperm flagellum
|
J:258613
|
asthenozoospermia
|
J:258613
|
coiled sperm flagellum
|
J:258613
|
kinked sperm flagellum
|
J:258613
|
oligozoospermia
|
J:258613
|
short sperm flagellum
|
J:258613
|
Cfap44em1Fzh/Cfap44em1Fzh
(involves: C57BL/6)
|
abnormal outer dense fiber morphology
|
J:258613
|
abnormal sperm axoneme morphology
|
J:258613
|
abnormal sperm flagellum morphology
|
J:258613
|
absent sperm axonemal central pair
|
J:258613
|
absent sperm flagellum
|
J:258613
|
asthenozoospermia
|
J:258613
|
coiled sperm flagellum
|
J:258613
|
kinked sperm flagellum
|
J:258613
|
oligozoospermia
|
J:258613
|
short sperm flagellum
|
J:258613
|
Cfap44em1Pfr/Cfap44+
(involves: C57BL/6J)
|
teratozoospermia
|
J:257803
|
Cfap44em1Pfr/Cfap44em1Pfr
(involves: C57BL/6J)
|
abnormal outer dense fiber morphology
|
J:257803
|
abnormal sperm axoneme morphology
|
J:257803
|
abnormal sperm fibrous sheath morphology
|
J:257803
|
abnormal sperm midpiece morphology
|
J:257803
|
abnormal sperm mitochondrial sheath morphology
|
J:257803
|
abnormal sperm principal piece morphology
|
J:257803
|
asthenozoospermia
|
J:257803
|
teratozoospermia
|
J:257803
|
Cfap45em1Hmd/Cfap45em1Hmd
(involves: C57BL/6)
|
abnormal motile primary cilium physiology
|
J:297786
|
asthenozoospermia
|
J:297786
|
decreased hyperactivated sperm motility
|
J:297786
|
Cfap47em1Fzh/Y
(C57BL/6-Cfap47em1Fzh)
|
abnormal sperm fibrous sheath morphology
|
J:307391
|
asthenozoospermia
|
J:307391
|
kinked sperm flagellum
|
J:307391
|
teratozoospermia
|
J:307391
|
Cfap52em1Cya/Cfap52em1Cya
(C57BL/6J-Cfap52em1Cya/Cya)
|
abnormal sperm flagellum morphology
|
J:338033
|
abnormal sperm mitochondrial sheath morphology
|
J:338033
|
asthenozoospermia
|
J:338033
|
decreased sperm progressive motility
|
J:338033
|
Cfap53em1Cya/Cfap53em1Cya
(involves: C57BL/6 * ICR)
|
abnormal sperm axoneme morphology
|
J:307591
|
abnormal sperm flagellum morphology
|
J:307591
|
abnormal sperm head morphology
|
J:307591
|
absent sperm flagellum
|
J:307591
|
coiled sperm flagellum
|
J:307591
|
elongated manchette
|
J:307591
|
oligozoospermia
|
J:307591
|
short sperm flagellum
|
J:307591
|
Cfap54Gt(IST10309B2)Tigm/Cfap54Gt(IST10309B2)Tigm
(B6J.B6N-Cfap54Gt(IST10309B2)Tigm)
|
abnormal brain ependyma motile cilium physiology
|
J:228444
|
abnormal respiratory motile cilium morphology
|
J:228444
|
abnormal respiratory motile cilium physiology
|
J:228444
|
absent brain ependyma motile cilia
|
J:228444
|
Cfap54Gt(IST10309B2)Tigm/Cfap54Gt(IST10309B2)Tigm
((B6J.B6N-Cfap54Gt(IST10309B2)Tigm x 129S6.B6N-Cfap54Gt(IST10309B2)Tigm)F1)
|
abnormal brain ependyma motile cilium physiology
|
J:228444
|
abnormal respiratory motile cilium morphology
|
J:228444
|
abnormal respiratory motile cilium physiology
|
J:228444
|
abnormal sperm axoneme morphology
|
J:228444
|
abnormal spermatid morphology
|
J:228444
|
absent sperm flagellum
|
J:228444
|
oligozoospermia
|
J:228444
|
short sperm flagellum
|
J:228444
|
Cfap57em1Qsh/Cfap57em1Qsh
(C57BL/6-Cfap57em1Qsh)
|
abnormal sperm axoneme morphology
|
J:333969
|
abnormal sperm flagellum morphology
|
J:333969
|
coiled sperm flagellum
|
J:333969
|
immotile sperm
|
J:333969
|
kinked sperm flagellum
|
J:333969
|
oligozoospermia
|
J:333969
|
short sperm flagellum
|
J:333969
|
Cfap58em1Fzh/Cfap58em1Fzh
(Not Specified)
|
asthenozoospermia
|
J:296991
|
coiled sperm flagellum
|
J:296991
|
decreased elongated spermatid number
|
J:296991
|
immotile sperm
|
J:296991
|
oligozoospermia
|
J:296991
|
short sperm flagellum
|
J:296991
|
Cfap61em1Mngx/Cfap61em1Mngx
(Not Specified)
|
abnormal sperm axoneme morphology
|
J:319365
|
abnormal sperm flagellum morphology
|
J:319365
|
abnormal sperm radial spoke morphology
|
J:319365
|
absent sperm flagellum
|
J:319365
|
coiled sperm flagellum
|
J:319365
|
immotile sperm
|
J:319365
|
kinked sperm flagellum
|
J:319365
|
oligozoospermia
|
J:319365
|
short sperm flagellum
|
J:319365
|
thick sperm flagellum
|
J:319365
|
Cfap61em1Yqt/Cfap61em1Yqt
(C57BL/6-Cfap61em1Yqt)
|
abnormal outer dense fiber morphology
|
J:333342
|
abnormal sperm axoneme morphology
|
J:333342
|
abnormal sperm flagellum morphology
|
J:333342
|
absent sperm flagellum
|
J:333342
|
asthenozoospermia
|
J:333342
|
coiled sperm flagellum
|
J:333342
|
decreased sperm progressive motility
|
J:333342
|
increased testis apoptosis
|
J:333342
|
oligozoospermia
|
J:333342
|
short sperm flagellum
|
J:333342
|
Cfap65em1Fzh/Cfap65em1Fzh
(involves: C57BL/6)
|
abnormal sperm axoneme morphology
|
J:292578
|
absent sperm axonemal central pair
|
J:292578
|
absent sperm flagellum
|
J:292578
|
asthenozoospermia
|
J:292578
|
coiled sperm flagellum
|
J:292578
|
increased male germ cell apoptosis
|
J:292578
|
short sperm flagellum
|
J:292578
|
Cfap65em1Yqt/Cfap65em1Yqt
(involves: C57BL/6 * C57BL/6N)
|
abnormal acrosome assembly
|
J:325402
|
abnormal acrosome morphology
|
J:325402
|
abnormal manchette assembly
|
J:325402
|
abnormal outer dense fiber morphology
|
J:325402
|
abnormal sperm axoneme morphology
|
J:325402
|
abnormal sperm connecting piece morphology
|
J:325402
|
abnormal sperm flagellum morphology
|
J:325402
|
abnormal sperm flagellum thickness
|
J:325402
|
abnormal sperm head morphology
|
J:325402
|
abnormal sperm mitochondrial sheath morphology
|
J:325402
|
abnormal sperm radial spoke morphology
|
J:325402
|
abnormal spermatid morphology
|
J:325402
|
absent acrosome
|
J:325402
|
absent sperm axonemal central pair
|
J:325402
|
absent sperm flagellum
|
J:325402
|
coiled sperm flagellum
|
J:325402
|
detached acrosome
|
J:325402
|
detached sperm flagellum
|
J:325402
|
ectopic manchette
|
J:325402
|
elongated manchette
|
J:325402
|
immotile sperm
|
J:325402
|
increased male germ cell apoptosis
|
J:325402
|
kinked sperm flagellum
|
J:325402
|
oligozoospermia
|
J:325402
|
short sperm flagellum
|
J:325402
|
teratozoospermia
|
J:325402
|
Cfap69em1Fzh/Cfap69em1Fzh
(involves: C57BL/6J)
|
abnormal acrosome morphology
|
J:288345
|
abnormal outer dense fiber morphology
|
J:288345
|
abnormal sperm axoneme morphology
|
J:288345
|
abnormal sperm flagellum morphology
|
J:288345
|
abnormal sperm head morphology
|
J:288345
|
absent sperm flagellum
|
J:288345
|
coiled sperm flagellum
|
J:288345
|
immotile sperm
|
J:288345
|
short sperm flagellum
|
J:288345
|
Cfap69tm1b(KOMP)Wtsi/Cfap69tm1b(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal outer dense fiber morphology
|
J:263440
|
abnormal sperm axoneme morphology
|
J:263440
|
abnormal sperm fibrous sheath morphology
|
J:263440
|
abnormal sperm flagellum morphology
|
J:263440
|
abnormal sperm head morphology
|
J:263440
|
abnormal sperm midpiece morphology
|
J:263440
|
abnormal sperm mitochondrial sheath morphology
|
J:263440
|
abnormal sperm principal piece morphology
|
J:263440
|
absent sperm fibrous sheath
|
J:263440
|
absent sperm flagellum
|
J:263440
|
ectopic manchette
|
J:263440
|
immotile sperm
|
J:263440
|
short sperm flagellum
|
J:263440
|
Cfap70em1Chnsr/Cfap70em1Chnsr
(involves: C57BL/6J)
|
abnormal brain ependyma motile cilium morphology
|
J:338031
|
abnormal outer dense fiber morphology
|
J:338031
|
abnormal sperm axoneme morphology
|
J:338031
|
abnormal sperm flagellum morphology
|
J:338031
|
asthenozoospermia
|
J:338031
|
coiled sperm flagellum
|
J:338031
|
decreased brain ependyma motile cilium number
|
J:338031
|
oligozoospermia
|
J:338031
|
short sperm flagellum
|
J:338031
|
Cfap70em2Chnsr/Cfap70em2Chnsr
(involves: C57BL/6J)
|
abnormal sperm axoneme morphology
|
J:338031
|
abnormal sperm flagellum morphology
|
J:338031
|
absent sperm axonemal central pair
|
J:338031
|
absent sperm flagellum
|
J:338031
|
asthenozoospermia
|
J:338031
|
coiled sperm flagellum
|
J:338031
|
oligozoospermia
|
J:338031
|
short sperm flagellum
|
J:338031
|
Cfap97d1em1Osb/Cfap97d1em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm axoneme morphology
|
J:294173
|
asthenozoospermia
|
J:294173
|
Cfap97d1tm1a(KOMP)Wtsi/Cfap97d1tm1a(KOMP)Wtsi
(involves: 129S/SvEv * C57BL/6N)
|
asthenozoospermia
|
J:294173
|
Cfap119em1Gaof/Cfap119em1Gaof
(involves: 129/SvEv * C57BL/6)
|
abnormal acrosome morphology
|
J:345163
|
abnormal manchette assembly
|
J:345163
|
abnormal sperm axoneme morphology
|
J:345163
|
abnormal sperm fibrous sheath morphology
|
J:345163
|
abnormal sperm flagellum morphology
|
J:345163
|
abnormal sperm head morphology
|
J:345163
|
abnormal sperm mitochondrial morphology
|
J:345163
|
asthenozoospermia
|
J:345163
|
cellular phenotype
|
J:345163
|
coiled sperm flagellum
|
J:345163
|
elongated manchette
|
J:345163
|
oligozoospermia
|
J:345163
|
short sperm flagellum
|
J:345163
|
teratozoospermia
|
J:345163
|
Cfap157tm1b(EUCOMM)Hmgu/Cfap157tm1b(EUCOMM)Hmgu
(involves: C57BL/6 * SJL)
|
abnormal cell morphology
|
J:237484
|
abnormal sperm flagellum morphology
|
J:237484
|
abnormal sperm head morphology
|
J:237484
|
abnormal sperm midpiece morphology
|
J:237484
|
abnormal sperm motility
|
J:237484
|
absent sperm head
|
J:237484
|
decreased hyperactivated sperm motility
|
J:237484
|
decreased male germ cell number
|
J:237484
|
Cfap157tm1d(EUCOMM)Hmgu/Cfap157tm1d(EUCOMM)Hmgu
(involves: C57BL/6 * SJL)
|
abnormal cell morphology
|
J:237484
|
abnormal sperm flagellum morphology
|
J:237484
|
abnormal sperm head morphology
|
J:237484
|
abnormal sperm midpiece morphology
|
J:237484
|
abnormal sperm motility
|
J:237484
|
absent sperm head
|
J:237484
|
decreased hyperactivated sperm motility
|
J:237484
|
decreased male germ cell number
|
J:237484
|
Cfap206em1Yxc/Cfap206em1Yxc
(C57BL/6-Cfap206em1Yxc)
|
abnormal outer dense fiber morphology
|
J:311499
|
abnormal sperm axoneme morphology
|
J:311499
|
abnormal sperm flagellum morphology
|
J:311499
|
absent sperm axonemal central pair
|
J:311499
|
absent sperm flagellum
|
J:311499
|
asthenozoospermia
|
J:311499
|
coiled sperm flagellum
|
J:311499
|
decreased sperm progressive motility
|
J:311499
|
kinked sperm flagellum
|
J:311499
|
oligozoospermia
|
J:311499
|
short sperm flagellum
|
J:311499
|
Cfap206tm1.2Gos/Cfap206tm1.2Gos
(involves: 129 * C57BL/6J * CD-1 * SJL)
|
abnormal sperm radial spoke morphology
|
J:293391
|
asthenozoospermia
|
J:293391
|
coiled sperm flagellum
|
J:293391
|
kinked sperm flagellum
|
J:293391
|
Cfdp1tm1Dkwpd/Cfdp1tm2.1Dkwpd E2f1Tg(Wnt1-cre)2Sor/E2f1+
(involves: 129 * 129S2/SvPas * C3H * C57BL/6)
|
abnormal intracellular organelle physiology
|
J:349245
|
Cfhtm1Mbo/Cfhtm1Mbo
(involves: 129/Sv * C57BL/6)
|
increased mesangial cell number
|
J:78193
|
mesangial cell interposition
|
J:78193
|
Cfiem1Jiwe/Cfiem1Jiwe
(involves: C57BL/6J)
|
increased mesangial cell number
|
J:308307
|
Cfl1c5/Cfl1c5 Vangl2Lp/Vangl2Lp
(involves: C57BL/6J * LPT/LeJ)
|
abnormal embryonic cilium location or orientation
|
J:194042
|
Cfl1tm1.1Wit/Cfl1tm1.1Wit
(involves: 129 * C57BL/6 * SJL)
|
abnormal axon extension
|
J:125317
|
abnormal neuron differentiation
|
J:125317
|
abnormal neuronal precursor proliferation
|
J:125317
|
premature neuronal precursor differentiation
|
J:125317
|
Cfl1tm1.2Wit/Cfl1tm1.2Wit
(involves: 129)
|
abnormal neural crest cell delamination
|
J:96452
|
abnormal neural crest cell migration
|
J:96452
|
Cflartm1Mak/Cflartm1Mak
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1))
|
increased fibroblast apoptosis
|
J:63049
|
Cflartm1Ywh/Cflartm1Ywh Tg(Lck-cre)548Jxm/0
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * CBA)
|
increased thymocyte apoptosis
|
J:100558
|
Cftrtm1.1Cwr/Cftrtm1.1Cwr
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:142723
|
Cftrtm1.1Sdw/Cftrtm1.1Sdw
(involves: C57BL/6 * C57BL/6J)
|
abnormal intestinal goblet cell morphology
|
J:323560
|
Cftrtm1Bay/Cftrtm1Bay
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal intestinal goblet cell morphology
|
J:15244
|
Cftrtm1Eur/Cftrtm1Eur
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal intestinal goblet cell morphology
|
J:28979
|
Cftrtm1Eur/Cftrtm1Eur
(B6.129P2-Cftrtm1Eur)
|
abnormal intestinal goblet cell morphology
|
J:189205
|
Cftrtm1Hgu/Cftrtm1Hgu
(CF/1Ztm)
|
abnormal ileal goblet cell morphology
|
J:112752
|
Cftrtm1Hgu/Cftrtm1Hgu
(CF/3Ztm)
|
abnormal ileal goblet cell morphology
|
J:112752
|
Cftrtm1Hsc/Cftrtm1Hsc
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal colon goblet cell morphology
|
J:31759
|
abnormal small intestine goblet cell morphology
|
J:31759
|
Cftrtm1Kth/Cftrtm1Kth
(B6.129S7-Cftrtm1Kth)
|
impaired sperm migration in female genital tract
|
J:145380
|
Cftrtm1Unc/Cftr+
(involves: 129P2/OlaHsd)
|
asthenozoospermia
|
J:122297
|
Cftrtm1Unc/Cftrtm1Unc
(B6.129P2-Cftrtm1Unc/J)
|
impaired sperm migration in female genital tract
|
J:145380
|
Cftrtm1Unc/Cftrtm1Unc
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
abnormal intestinal goblet cell morphology
|
J:21934
|
Cftrtm1Unc/Cftrtm1Unc Tg(FABPCFTR)1Jaw/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
abnormal colon goblet cell morphology
|
J:21934
|
Cftrtm2Hgu/Cftrtm2Hgu
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:74740
|
Cgatm1Sac/Cgatm1Sac
(involves: 129S2/SvPas * C57BL/6J)
|
arrest of male meiosis
|
J:28450
|
Chaf1atm1Ger/Chaf1atm1Ger
(involves: 129S2/SvPasCrl)
|
abnormal cell nucleus morphology
|
J:116133
|
Chaf1btm2c(EUCOMM)Hmgu/Chaf1b+ Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
increased apoptosis
|
J:266848
|
Chaf1btm2c(EUCOMM)Hmgu/Chaf1btm2c(EUCOMM)Hmgu Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
increased apoptosis
|
J:266848
|
Chchd2tm1Noha/Chchd2tm1Noha
(C57BL/6-Chchd2tm1Noha)
|
abnormal mitochondrial matrix morphology
|
J:307383
|
abnormal mitochondrial shape
|
J:307383
|
decreased mitochondrial size
|
J:307383
|
disorganized mitochondrial cristae
|
J:307383
|
impaired autophagy
|
J:307383
|
Chchd4Gt(IST11943B12)Tigm/Chchd4+
(involves: C57BL/6N)
|
cellular phenotype
|
J:250035
|
Chchd4Gt(IST11943B12)Tigm/Chchd4Gt(IST11943B12)Tigm
(involves: C57BL/6N)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:256078
|
Chchd10em3Dpn/Chchd10em3Dpn
(C57BL/6J-Chchd10em3Dpn)
|
abnormal mitochondrial crista morphology
|
J:344465
|
abnormal mitochondrial physiology
|
J:344465
|
decreased myocardial fiber mitochondrial DNA content
|
J:344465
|
Chchd10em3Dpn/Chchd10em3Dpn Oma1tm1Otin/Oma1+
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl)
|
abnormal mitochondrial crista morphology
|
J:344465
|
abnormal mitochondrial morphology
|
J:344465
|
abnormal muscle fiber mitochondrial morphology
|
J:344465
|
dilated mitochondrion
|
J:344465
|
Chchd10em3Dpn/Chchd10em3Dpn Oma1tm1Otin/Oma1tm1Otin
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl)
|
abnormal mitochondrial crista morphology
|
J:344465
|
abnormal mitochondrial shape
|
J:344465
|
dilated mitochondrion
|
J:344465
|
Chchd10em5Lutzy/Chchd10em5Lutzy
(C57BL/6J-Chchd10em5Lutzy/J)
|
abnormal respiratory electron transport chain
|
J:254726
|
cellular phenotype
|
J:254726
|
Chchd10em8Lutzy/Chchd10+
(C57BL/6NJ-Chchd10em8Lutzy/J)
|
abnormal cell nucleus morphology
|
J:272524
|
abnormal mitochondrial crista morphology
|
J:272524
|
abnormal mitochondrial matrix morphology
|
J:272524
|
abnormal mitochondrial morphology
|
J:272524
|
abnormal vacuole morphology
|
J:272524
|
cardiac interstitial fibrosis
|
J:272524
|
increased mitochondrial number
|
J:272524
|
Chd1tm1b(KOMP)Rsan/Chd1tm1b(KOMP)Rsan
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle
|
J:217689
|
increased embryonic epiblast cell apoptosis
|
J:217689
|
Chd2Gt(RRBO46)Byg/Chd2Gt(RRBO46)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle
|
J:146176
|
abnormal DNA repair
|
J:146176
|
increased cellular sensitivity to methylmethanesulfonate
|
J:146176
|
increased cellular sensitivity to ultraviolet irradiation
|
J:146176
|
increased cellular sensitivity to X-ray irradiation
|
J:146176
|
Chd4em1Flc/Chd4em1Flc
(C57BL/6J-Chd4em1Flc)
|
increased fetal cardiomyocyte proliferation
|
J:338019
|
Chd4Gt(RRO120)Byg/Chd4Gt(RRO120)Byg
(B6.129P2-Chd4Gt(RRO120)Byg)
|
increased apoptosis
|
J:224146
|
Chd4tm1.1Kge/Chd4tm1.2Kge Tg(CAG-Bgeo/GFP)21Lbe/0 Tg(Lck-cre)1Cwi/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal cell cycle
|
J:109547
|
decreased T cell proliferation
|
J:109547
|
Chd4tm1.2Kge/Chd4tm1.2Kge Tg(Lck-cre)1Cwi/0
(involves: C57BL/6 * DBA/2 * SJL)
|
abnormal cell cycle
|
J:109547
|
decreased T cell proliferation
|
J:109547
|
Chd5tm1.2Gmbr/Chd5tm1.2Gmbr
(involves: 129S4/SvJae)
|
abnormal male germ cell morphology
|
J:207846
|
abnormal spermatid morphology
|
J:207846
|
asthenozoospermia
|
J:207846
|
decreased male germ cell number
|
J:207846
|
oligozoospermia
|
J:207846
|
teratozoospermia
|
J:207846
|
Chd7Gt(S20-7E1)Sor/Chd7+
(involves: 129S4/SvJaeSor)
|
abnormal neuronal precursor proliferation
|
J:164582
|
Chd7Gt(S20-7E1)Sor/Chd7+
(129S1.129S4(B6)-Chd7Gt(S20-7E1)Sor)
|
abnormal neuron differentiation
|
J:174086
|
abnormal olfactory epithelium cilium morphology
|
J:148116
|
decreased apoptosis
|
J:174086
|
decreased cell proliferation
|
J:174086
|
Chd7Gt(S20-7E1)Sor/Chd7Gt(S20-7E1)Sor
(involves: 129S4/SvJaeSor)
|
abnormal neuronal precursor proliferation
|
J:164582
|
Chd7Gt(S20-7E1)Sor/Chd7Gt(S20-7E1)Sor
(129S1.129S4(B6)-Chd7Gt(S20-7E1)Sor)
|
decreased cell proliferation
|
J:174086
|
Chd7Gt(S20-7E1)Sor/Chd7tm1.1Dmm Foxg1tm1(cre)Skm/Foxg1+
(involves: 129 * C57BL/6 * Swiss Webster)
|
abnormal neuronal precursor proliferation
|
J:164582
|
Chd7Gt(XK403)Byg/Chd7+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neural crest cell migration
|
J:154590
|
Chd7Ome/Chd7+
(involves: BALB/cByJ * C57BL/6J)
|
increased middle ear goblet cell number
|
J:187200
|
Chd7tm1.1Dmm/Chd7tm1.1Dmm Tg(Pdgfra-cre/ERT)467Dbe/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal oligodendrocyte apoptosis
|
J:264451
|
decreased oligodendrocyte progenitor number
|
J:264451
|
Chd7tm2a(EUCOMM)Wtsi/Chd7tm2a(EUCOMM)Wtsi
(involves: 129S6/SvEvTac * C57BL/6N)
|
abnormal epigenetic regulation of gene expression
|
J:207089
|
decreased fetal cardiomyocyte proliferation
|
J:207089
|
increased cardiomyocyte apoptosis
|
J:207089
|
Chd7tm2a(EUCOMM)Wtsi/Chd7tm2a(EUCOMM)Wtsi E2f1Tg(Wnt1-cre)2Sor/E2f1+ Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
(involves: 129 * C3H * C57BL/6 * C57BL/6N)
|
abnormal cranial neural crest cell migration
|
J:298597
|
Chd7tm2c(EUCOMM)Wtsi/Chd7tm2c(EUCOMM)Wtsi Slc1a3tm1(cre/ERT2)Mgoe/Slc1a3+
(involves: 129S2/SvPas * C57BL/6 * C57BL/6N * SJL)
|
increased neuron apoptosis
|
J:222062
|
Chd7tm2c(EUCOMM)Wtsi/Chd7tm2c(EUCOMM)Wtsi Tg(Atoh1-cre)1Bfri/0
(involves: C57BL/6 * C57BL/6J * C57BL/6N * CBA)
|
decreased cerebellar granule cell precursor proliferation
|
J:242933
|
increased cellular sensitivity to oxidative stress
|
J:314588
|
increased neuron apoptosis
|
J:242933
|
Chd7tm2c(EUCOMM)Wtsi/Chd7tm2c(EUCOMM)Wtsi Tg(Atoh1-cre)1Bfri/0
(involves: C57BL/6 * C57BL/6N * CBA)
|
increased neuron apoptosis
|
J:243947
|
premature neuronal precursor differentiation
|
J:243947
|
Chd7tm2c(EUCOMM)Wtsi/Chd7tm2c(EUCOMM)Wtsi Tg(Gdf9-icre)5092Coo/0
(involves: C57BL/6 * C57BL/6J * C57BL/6N)
|
increased granulosa cell apoptosis
|
J:324165
|
Chd8tm1Kei/Chd8tm1Kei
(involves: C57BL/6)
|
increased ectoderm apoptosis
|
J:92968
|
Chd9em1Ibbr/Chd9em1Ibbr
(C57BL/6N-Chd9em1Ibbr)
|
abnormal oocyte morphology
|
J:270181
|
Chd9em2Ibbr/Chd9em2Ibbr
(C57BL/6N-Chd9em2Ibbr)
|
abnormal oocyte morphology
|
J:270181
|
Chdhtm1Zei/Chdhtm1Zei
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal mitochondrial crista morphology
|
J:162343
|
abnormal respiratory electron transport chain
|
J:162343
|
asthenozoospermia
|
J:162343
|
dilated mitochondrion
|
J:162343
|
Chek1tm1Jmr/Chek1+ Tg(Wap-cre)11738Mam/0
(involves: C57BL/6)
|
increased cell proliferation
|
J:91266
|
Chek1tm1Jmr/Chek1tm1Jmr Tg(Dct-lacZ)A12Jkn/0 Tg(Tyr-cre)1Lru/Y
(involves: C57BL/6 * CBA * DBA/2)
|
abnormal DNA replication
|
J:265850
|
Chek1tm1Jmr/Chek1tm1Jmr Tg(Wap-cre)11738Mam/0
(involves: C57BL/6)
|
abnormal apoptosis
|
J:91266
|
decreased cell proliferation
|
J:91266
|
Chek1tm1Mkt/Chek1tm1Mkt
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle checkpoint function
|
J:62918
|
abnormal cell nucleus morphology
|
J:62918
|
abnormal inner cell mass proliferation
|
J:62918
|
absent inner cell mass proliferation
|
J:62918
|
increased inner cell mass apoptosis
|
J:62918
|
Chek1tm1Sje/Chek1tm1Sje
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:62919
|
decreased cell proliferation
|
J:62919
|
increased embryonic tissue cell apoptosis
|
J:62919
|
Chek1tm1Sje/Chek1tm1Sje Trp53tm1Brd/Trp53tm1Brd
(involves: 129S7/SvEvBrd)
|
increased apoptosis
|
J:62919
|
Chek1tm2.1Sje/Chek1+ Trp53tm1Brn/Trp53+ Tg(MMTV-cre)#Mam/0
(involves: 129P2/OlaHsd * FVB)
|
abnormal chromosome morphology
|
J:162126
|
aneuploidy
|
J:162126
|
Chek2tm1b(EUCOMM)Hmgu/Chek2tm1b(EUCOMM)Hmgu Prdm9tm1Ymat/Prdm9tm1Ymat
(B6.Cg-Chek2tm1b(EUCOMM)Hmgu Prdm9tm1Ymat)
|
abnormal chiasmata formation
|
J:299008
|
abnormal female meiosis
|
J:299008
|
abnormal female meiosis I arrest
|
J:299008
|
decreased oocyte number
|
J:299008
|
Chek2tm1Mak/Chek2tm1Mak
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:78491
|
decreased cellular sensitivity to gamma-irradiation
|
J:78491
|
Chek2tm1Mak/Chek2tm1Mak
(involves: 129P2/OlaHsd)
|
decreased cellular sensitivity to ionizing radiation
|
J:126186
|
Chek2tm1Mak/Chek2tm1Mak Swsap1em1Mjn/Swsap1em1Mjn
(involves: 129P2/OlaHsd * C57BL/6J * CBA/J)
|
abnormal chromosomal synapsis
|
J:268570
|
decreased oocyte number
|
J:268570
|
oligozoospermia
|
J:268570
|
Chek2tm1Mak/Chek2tm1Mak Zswim7em1Mjn/Zswim7em1Mjn
(involves: 129P2/OlaHsd * C57BL/6J * CBA/J)
|
oligozoospermia
|
J:268570
|
Chek2tm1Nmt/Chek2tm1Nmt
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cellular sensitivity to ionizing radiation
|
J:88888
|
Chek2tm1Pjs/Chek2tm1Pjs
(involves: 129/Sv * Black Swiss * FVB/N)
|
abnormal cell cycle
|
J:118262
|
abnormal cell physiology
|
J:118262
|
polyploidy
|
J:118262
|
Chfrtm1Jc/Chfrtm1Jc
(involves: 129S/SvEv * C57BL/6)
|
abnormal mitosis
|
J:97428
|
chromosome breakage
|
J:97428
|
Chi3l1tm1Eli/Chi3l1tm1Eli
(B6.Cg-Chi3l1tm1Eli)
|
decreased splenocyte proliferation
|
J:148490
|
increased apoptosis
|
J:148490
|
increased T cell apoptosis
|
J:148490
|
Chmp1aGt(XC472)Byg/Chmp1aGt(XC472)Byg
(B6.129P2-Chmp1aGt(XC472)Byg)
|
decreased cerebellar granule cell precursor proliferation
|
J:271138
|
decreased neuronal precursor proliferation
|
J:271138
|
Chmp2btm1.1Hiok/Chmp2b+
(involves: C57BL/6J)
|
abnormal cell cycle checkpoint function
|
J:308471
|
abnormal endoplasmic reticulum morphology
|
J:308471
|
cellular necrosis
|
J:308471
|
Chmp5tm1Gho/Chmp5tm1Gho
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell physiology
|
J:107913
|
abnormal intracellular organelle morphology
|
J:107913
|
Chn1tm1.1Abet/Chn1tm1.1Abet
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal axon extension
|
J:128724
|
Chn1tm1.1Ece/Chn1tm1.1Ece Tg(Hlxb9-GFP)1Tmj/0
(involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J)
|
abnormal axon fasciculation
|
J:243785
|
Chn1tm2Abet/Chn1tm2Abet
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal axon extension
|
J:128724
|
Chn2tm1.1Alk/Chn2tm1.1Alk
(involves: C57BL/6 * CD-1 * FVB/N)
|
abnormal axon pruning
|
J:186252
|
Chn2tm2.1Alk/Chn2tm2.1Alk
(B6.Cg-Chn2tm2.1Alk)
|
abnormal axon pruning
|
J:186252
|
Chordc1tm1Mbra/Chordc1+
(involves: 129 * C57BL/6)
|
abnormal centrosome morphology
|
J:222040
|
Chordc1tm1Mbra/Chordc1tm1Mbra
(Not Specified)
|
abnormal inner cell mass apoptosis
|
J:159109
|
abnormal trophoblast giant cell proliferation
|
J:159109
|
absent inner cell mass proliferation
|
J:159109
|
Chrdtm1Emdr/Chrdtm1Emdr
(either: B6SJL.129-Chrdtm1Emdr or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J))
|
abnormal neural crest cell migration
|
J:83662
|
Chrna7tm1Bay/Chrna7tm1Bay
(B6.129S7-Chrna7tm1Bay/J)
|
asthenozoospermia
|
J:115434
|
Chrna7tm1Bay/Chrna7tm1Bay
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal airway basal cell differentiation
|
J:154705
|
Chrna7tm2Bay/Chrna7tm2Bay
(involves: 129S7/SvEvBrd * C57BL/6J)
|
increased neuron apoptosis
|
J:61536
|
Chrnb2tm1Jpc/Chrnb2tm1Jpc
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:103908
|
Chst1tm1(KOMP)Vlcg/Chst1tm1(KOMP)Vlcg Chst2tm1Tmu/Chst2tm1Tmu Chst4tm1Sdr/Chst4tm1Sdr
(involves: 129S2/SvPas * C57BL/6NTac)
|
abnormal leukocyte migration
|
J:204813
|
Chst2tm1Tmu/Chst2tm1Tmu
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal leukocyte migration
|
J:92231
|
Chst2tm1Tmu/Chst2tm1Tmu Chst4tm1Sdr/Chst4tm1Sdr
(involves: 129S2/SvPas)
|
abnormal leukocyte migration
|
J:204813
|
Chst3tm1Tmu/Chst3tm1Tmu
(involves: 129S2/SvPas)
|
increased T cell proliferation
|
J:217719
|
Chst4tm1Mifu/Chst4tm1Mifu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:113195
|
impaired leukocyte tethering or rolling
|
J:113195
|
Chst4tm1Mifu/Chst4tm1Mifu Gcnt1tm1Jxm/Gcnt1tm1Jxm
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:113195
|
impaired leukocyte tethering or rolling
|
J:113195
|
Chst4tm1Sdr/Chst4tm1Sdr
(involves: C57BL/6)
|
abnormal leukocyte adhesion
|
J:86759
|
abnormal leukocyte migration
|
J:86759
|
Chst14tm1.1Msch/Chst14tm1.1Msch
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal axon extension
|
J:203583
|
increased Schwann cell proliferation
|
J:203583
|
Chsy1skt/Chsy1skt Pde6b+/Pde6b+
(mixed)
|
abnormal extracellular matrix morphology
|
J:286529
|
Chtf18tm1.1KhK/Chtf18tm1.1KhK
(Not Specified)
|
abnormal male germ cell morphology
|
J:194119
|
abnormal male meiosis
|
J:194119
|
increased male germ cell apoptosis
|
J:194119
|
oligozoospermia
|
J:194119
|
Chtf18tm1.1KhK/Chtf18tm1.2Khk Alpltm1(cre)Nagy/Alpl+
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal male germ cell morphology
|
J:194119
|
Chuktm1.1Mpa/Chuktm1.1Mpa
(involves: C57BL/6)
|
abnormal keratinocyte differentiation
|
J:122320
|
Chuktm1Aki/Chuktm1Aki
(involves: 129P2/OlaHsd)
|
abnormal keratinocyte differentiation
|
J:54315
|
cellular phenotype
|
J:54315
|
Chuktm1Lex/Chuktm1Lex Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: 129S/Sv * 129S/SvEvBrd * C57BL/6)
|
abnormal fibroblast migration
|
J:159873
|
decreased fibroblast cell migration
|
J:159873
|
decreased fibroblast chemotaxis
|
J:159873
|
Chuktm1Lex/Chuktm1Lex Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S/SvEvBrd)
|
impaired macrophage chemotaxis
|
J:159873
|
impaired neutrophil chemotaxis
|
J:159873
|
Chuktm1Mka/Chuktm1Mka
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA)
|
abnormal keratinocyte differentiation
|
J:54316
|
cellular phenotype
|
J:54316
|
Chuktm1Mpa/Chuktm1Mpa Tg(KRT14-cre)1Cgn/?
(involves: C57BL/6)
|
abnormal keratinocyte differentiation
|
J:122320
|
Chuktm1Ver/Chuktm1Ver
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell physiology
|
J:55415
|
abnormal keratinocyte differentiation
|
J:55415
|
Chuktm1Ver/Chuktm1Ver Ikbkbtm1Ver/Ikbkbtm1Ver
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell physiology
|
J:63443
|
increased embryonic neuroepithelium apoptosis
|
J:63443
|
increased hepatocyte apoptosis
|
J:63443
|
increased hindbrain apoptosis
|
J:63443
|
increased spinal cord apoptosis
|
J:63443
|
Chuktm1Yhu/Chuktm1Yhu Tg(KRT5-cre)5132Jlj/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:141162
|
increased keratinocyte proliferation
|
J:141162
|
Chuktm2Yhu/Chuktm2Yhu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased keratinocyte proliferation
|
J:197037
|
Cib1tm1Prse/Cib1tm1Prse
(involves: 129S6/SvEvTac * C57BL/6)
|
azoospermia
|
J:114645
|
decreased cell proliferation
|
J:114645
|
Cib2em1Xuzg/Cib2em1Xuzg
(C57BL/6-Cib2em1Xuzg)
|
abnormal inner hair cell kinocilium morphology
|
J:280151
|
Cib4em1Osb/Cib4em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm head morphology
|
J:293869
|
decreased elongated spermatid number
|
J:293869
|
Cidectm1.1Gonz/Cidectm1.2Gonz Tg(Fabp4-cre)#Abel/?
(B6N.Cg-Cidectm1.1Gonz/Cidectm1.2Gonz Tg(Fabp4-cre)#Abel)
|
increased adipocyte glucose uptake
|
J:226899
|
Ciitatm1Ccum/Ciitatm1Ccum
(involves: 129S2/SvPas * C57BL/6J)
|
decreased T cell proliferation
|
J:31601
|
Cilk1tm1.1Zfu/Cilk1tm1.1Zfu
(B6.Cg-Cilk1tm1.1Zfu/Zfu)
|
abnormal primary cilium morphology
|
J:309653
|
decreased mesenchymal cell proliferation involved in lung development
|
J:309653
|
enhanced autophagy
|
J:309653
|
Cilk1tm1a(KOMP)Mbp/Cilk1tm1a(KOMP)Mbp
(C57BL/6N-Cilk1tm1a(KOMP)Mbp)
|
abnormal primary cilium morphology
|
J:211652
|
Cimap2Retro/Cimap2Retro
(involves: C57BL/6J)
|
increased T cell proliferation
|
J:223336
|
Cimap3tm1.1Heli/Cimap3+
(chimera involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal cell physiology
|
J:162627
|
abnormal cilium morphology
|
J:162627
|
abnormal mitosis
|
J:162627
|
abnormal motile primary cilium morphology
|
J:162627
|
abnormal motile primary cilium physiology
|
J:162627
|
Cimap3tm2.1Heli/Cimap3tm2.1Heli
(involves: 129S6/SvEvTac * C57BL/6J * SJL)
|
cellular phenotype
|
J:244372
|
Cinda1BALB/c/?
(involves: BALB/c * CcS-4/Dem)
|
increased T cell proliferation
|
J:40728
|
Cinda2STS/A/?
(involves: BALB/c * CcS-4/Dem)
|
increased T cell proliferation
|
J:40728
|
Cinda3O20/A/Cinda3O20/A
(involves: O20/A * OcB-9/Dem)
|
decreased T cell proliferation
|
J:95917
|
Cinda3OcB9/Dem/Cinda3O20/A
(involves: O20/A * OcB-9/Dem)
|
increased T cell proliferation
|
J:95917
|
Cinda4OcB9/Dem/Cinda4O20/A
(involves: O20/A * OcB-9/Dem)
|
increased T cell proliferation
|
J:95917
|
Cinda4OcB9/Dem/Cinda4OcB9/Dem
(involves: O20/A * OcB-9/Dem)
|
increased T cell proliferation
|
J:95917
|
Cinda5OcB9/Dem/Cinda5O20/A
(involves: O20/A * OcB-9/Dem)
|
increased T cell proliferation
|
J:95917
|
Cinda5OcB9/Dem/Cinda5OcB9/Dem
(involves: O20/A * OcB-9/Dem)
|
increased T cell proliferation
|
J:95917
|
Cip2aGt(CD0252)Wtsi/Cip2aGt(CD0252)Wtsi
(involves: 129P2/OlaHsd * C57BL/6J)
|
oligozoospermia
|
J:187134
|
Cirbilem1Cya/Cirbilem1Cya
(Not Specified)
|
increased cardiomyocyte apoptosis
|
J:301260
|
Cirbptm1Jfuji/Cirbptm1Jfuji
(B6.129S2-Cirbptm1Jfuji)
|
abnormal cell cycle
|
J:186425
|
abnormal spermatogonia proliferation
|
J:186425
|
decreased fibroblast proliferation
|
J:186425
|
decreased spermatogonia number
|
J:186425
|
Cirozb2b1167Clo/Cirozb2b1167Clo
(C57BL/6J-Cirozb2b1167Clo)
|
immotile respiratory cilia
|
J:175213
|
Cisd1Gt(OST205742)Lex/Cisd1Gt(OST205742)Lex
(involves: 129S5/SvEvBrd)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:120125
|
Cisd2Gt(XS0445)Wtsi/Cisd2Gt(XS0445)Wtsi
(B6.129P2-Cisd2Gt(XS0445)Wtsi)
|
abnormal mitochondrial crista morphology
|
J:183788
|
abnormal mitochondrial shape
|
J:183788
|
enhanced autophagy
|
J:183788
|
increased mitochondrial size
|
J:183788
|
Cisd2tm1Tfts/Cisd2tm1Tfts
(B6.129S7-Cisd2tm1Tfts)
|
abnormal mitochondrial morphology
|
J:148467
|
abnormal respiratory electron transport chain
|
J:148467
|
Cishtm1.2Cdon/Cishtm1.2Cdon
(B6.129S6(Cg)-Cishtm1.2Cdon)
|
increased T cell proliferation
|
J:204829
|
Cittm1Fdc/Cittm1Fdc
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal spermatogonia proliferation
|
J:80899
|
decreased male germ cell number
|
J:80899
|
increased male germ cell apoptosis
|
J:80899
|
increased neuron apoptosis
|
J:80899
|
Cited1tm1Dunw/Cited1+
(B6.129P2-Cited1tm1Dunw)
|
paternal imprinting
|
J:87595
|
Cited2tm1Jpmb/Cited2tm1Jpmb
(involves: 129P2/OlaHsd * C57BL/6)
|
increased embryonic neuroepithelium apoptosis
|
J:74736
|
Ciz1tm1.1Homy/Ciz1tm1.1Homy
(involves: 129P2/OlaHsd * C57BL/6 * DBA)
|
cellular phenotype
|
J:198470
|
increased cellular sensitivity to hydroxyurea
|
J:198470
|
Ckmtm1Bew/Ckmtm1Bew
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cellular respiration
|
J:76699
|
Cks1btm1Sir/Cks1btm1Sir
(Not Specified)
|
early cellular replicative senescence
|
J:121692
|
Cks1btm1Sir/Cks1btm1Sir Tg(IghMyc)22Bri/?
(involves: C57BL * C57BL/6 * SJL)
|
decreased B cell proliferation
|
J:121564
|
Cks2tm1Sir/Cks2tm1Sir
(Not Specified)
|
abnormal female meiosis
|
J:99997
|
arrest of male meiosis
|
J:99997
|
azoospermia
|
J:99997
|
multinucleated giant male germ cells
|
J:99997
|
Clasp2tm1Gal/Clasp2tm1Gal
(Not Specified)
|
abnormal cell migration
|
J:116121
|
abnormal cell physiology
|
J:116121
|
Clcc1m1J/Clcc1m1J
(B6.C3Sn(Cg)-Clcc1m1J/SlacJ)
|
increased endoplasmic reticulum stress
|
J:218443
|
Clcn2nmf240/Clcn2nmf240
(C57BL/6J-Clcn2nmf240/J)
|
azoospermia
|
J:160207
|
Clcn2nmf289/Clcn2nmf289
(CByJ.Cg-Clcn2nmf289/Pjn)
|
azoospermia
|
J:243745
|
Clcn2tm1Mlv/Clcn2tm1Mlv
(involves: C57BL/6)
|
abnormal male germ cell morphology
|
J:77673
|
azoospermia
|
J:77673
|
Clcn2tm1Tjj/Clcn2tm1Tjj
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal male germ cell morphology
|
J:68137
|
abnormal spermatocyte morphology
|
J:68137
|
azoospermia
|
J:68137
|
Clcn3tm1Lamb/Clcn3tm1Lamb
(involves: 129S1/Sv * 129X1/SvJ)
|
impaired neutrophil phagocytosis
|
J:112692
|
Clcn5tm1Tjj/Y
(involves: 129)
|
abnormal cell physiology
|
J:160701
|
Clcn5tm1Tjj/Clcn5+ Clcn7tm3.1Tjj/Clcn7tm3.1Tjj Tg(APOE-cre)VITew/0
(involves: 129/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J)
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:155176
|
Clcn5tm2.1Tjj/Y
(involves: 129P2/OlaHsd * 129X1/SvJ * BALB/cJ * C57BL/6)
|
abnormal cell physiology
|
J:160701
|
Clcn5tm3.1Tjj/Y
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6)
|
cellular phenotype
|
J:160701
|
Clcn6tm1Tjj/Clcn6tm1Tjj
(involves: 129S1/Sv * 129X1/SvJ)
|
lysosomal protein accumulation
|
J:113752
|
Clcn7tm1.1Lex/Clcn7tm1.1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
lysosomal protein accumulation
|
J:186049
|
Clcn7tm2Tjj/Clcn7tm2Tjj
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal autophagy
|
J:217031
|
Clcn7tm2Tjj/Clcn7tm2Tjj
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal lysosome physiology
|
J:155176
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:155176
|
enhanced autophagy
|
J:155176
|
Clcn7tm3.1Tjj/Clcn7tm3.1Tjj Emx1tm1.1(cre)Ito/Emx1+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6)
|
abnormal lysosome physiology
|
J:155176
|
Clcn7tm3.1Tjj/Clcn7tm3.1Tjj Tg(APOE-cre)VITew/0
(B6.Cg-Clcn7tm3.1Tjj Tg(APOE-cre)VITew)
|
abnormal lysosome physiology
|
J:155176
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:155176
|
Clcn7tm4.1Tjj/Clcn7tm4.1Tjj
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal autophagy
|
J:217031
|
abnormal lysosome physiology
|
J:160702
|
Clcn7tm5.1Tjj/Clcn7tm5.1Tjj
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal lysosome morphology
|
J:217031
|
abnormal lysosome physiology
|
J:217031
|
cellular phenotype
|
J:217031
|
Cldn4tm1.1Yham/Cldn4tm1.1Yham
(B6.129S2-Cldn4tm1.1Yham)
|
increased kidney cell proliferation
|
J:195766
|
Cldn11tm1Ral/Cldn11tm1Ral
(Not Specified)
|
azoospermia
|
J:59025
|
Cldn15tm1Sats/Cldn15tm1Sats
(involves: C57BL/6)
|
abnormal duodenal goblet cell morphology
|
J:135596
|
abnormal enterocyte proliferation
|
J:135596
|
abnormal jejunal goblet cell morphology
|
J:135596
|
Cldn17em#Prso/Cldn17em#Prso
(C57BL/6-Cldn17em#Prso)
|
oxidative stress
|
J:325994
|
Cldn18tm1Lex/Cldn18tm1Lex
(involves: 129S5/SvEvBrd)
|
abnormal osteoclast differentiation
|
J:195931
|
Clec1atm1Yiw/Clec1atm1Yiw
(involves: C57BL/6J * C57BL/6NSlc)
|
decreased CD8-positive, alpha-beta memory T cell proliferation
|
J:329240
|
Clec2dtm1.1Mgil/Clec2dtm1.1Mgil
(C57BL/6-Clec2dtm1.1Mgil)
|
abnormal osteoblast physiology
|
J:143122
|
abnormal osteoclast differentiation
|
J:143122
|
Clec2htm1.1Apma/Clec2htm1.1Apma Rag1tm1Mom/Rag1tm1Mom
(B6.Cg-Rag1tm1Mom Clec2htm1.1Apma)
|
increased mesangial cell number
|
J:322835
|
Clec4a2tm1.1Cfg/Clec4a2tm1.1Cfg
(involves: C57BL/6)
|
increased B cell proliferation
|
J:217719
|
Clec4dtm1.1Cfg/Clec4dtm1.1Cfg
(involves: C57BL/6)
|
decreased B cell proliferation
|
J:217719
|
decreased T cell proliferation
|
J:217719
|
Clec4ntm1.2Mgne/Clec4ntm1.2Mgne
(involves: C57BL/6 * C57BL/6J)
|
impaired macrophage phagocytosis
|
J:209284
|
impaired neutrophil phagocytosis
|
J:209284
|
Clec7atm1.1Bpip/Clec7atm1.1Bpip Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6J)
|
impaired macrophage phagocytosis
|
J:203908
|
Clec11aem1Sjm/Clec11aem1Sjm
(involves: C57BL/6 * C57BL/Ka)
|
impaired osteoblast differentiation
|
J:239391
|
Clec12atm1Gdb/Clec12atm1Gdb
(involves: C57BL/6)
|
abnormal autophagy
|
J:224869
|
Clec12atm1Jrld/Clec12atm1Jrld
(B6J.129-Clec12atm1Jrld)
|
oxidative stress
|
J:210326
|
Clec16atm1.1Hhak/Clec16atm1.1Hhak Ndor1Tg(UBC-cre/ERT2)1Ejb/0
(involves: 129S/SvEv * C57BL/6 * SJL)
|
abnormal mitophagy
|
J:214528
|
Clec16atm1.1Hhak/Clec16atm1.1Hhak Tg(Pdx1-cre)1Herr/0
(involves: C57BL/6 * C57BL/6J * CBA/J * SJL)
|
abnormal endoplasmic reticulum morphology
|
J:214528
|
abnormal mitochondrial morphology
|
J:214528
|
abnormal mitophagy
|
J:214528
|
disorganized mitochondrial cristae
|
J:214528
|
increased mitochondrial size
|
J:214528
|
Clic4tm1.1Thor/Clic4tm1.1Thor Ins1tm1.1(cre)Thor/Ins1+
(involves: C57BL/6J)
|
decreased pancreatic islet cell apoptosis
|
J:223517
|
Clic4tm1.1Yus/Clic4tm1.1Yus
(involves: 129S4/SvJae * C57BL/6J)
|
decreased keratinocyte adhesion
|
J:185541
|
decreased keratinocyte migration
|
J:185541
|
impaired macrophage phagocytosis
|
J:183611
|
Clip1tm1.1Gal/Clip1tm1.1Gal
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal manchette morphology
|
J:102107
|
abnormal spermatid morphology
|
J:102107
|
Clip1tm1Gal/Clip1tm1Gal
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal manchette morphology
|
J:102107
|
abnormal sperm flagellum morphology
|
J:102107
|
abnormal sperm head morphology
|
J:102107
|
abnormal spermatid morphology
|
J:102107
|
ectopic manchette
|
J:102107
|
teratozoospermia
|
J:102107
|
Clip1tm1Gal/Clip1tm1Gal
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:116121
|
Clip2tm1.1Gal/Clip2tm1.1Gal
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell morphology
|
J:78711
|
Clk2tm1.1Ppgr/Clk2tm1.1Ppgr Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6NTac * FVB/N)
|
abnormal fatty acid oxidation
|
J:229283
|
Cln3em1Dprc/Cln3em1Dprc
(C57BL/6-Cln3em1Dprc)
|
abnormal lysosome morphology
|
J:294634
|
Cln3tm1Blda/Cln3tm1Blda
(B6.129-Cln3tm1Blda)
|
abnormal lysosome morphology
|
J:125194
|
Cln3tm1Mkat/Cln3tm1Mkat
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal lysosome morphology
|
J:57155
|
Cln3tm1Nbm/Cln3tm1Nbm
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
abnormal lysosome morphology
|
J:58230
|
Cln3tm1Nbm/Cln3tm1Nbm
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal cell adhesion
|
J:233445
|
Clns1atm1Kwn/Clns1atm1Kwn
(involves: 129 * C57BL/6J)
|
abnormal cell death
|
J:61831
|
Clockm1Jt/Clockm1Jt
(involves: C57BL/6J)
|
increased pancreatic islet cell apoptosis
|
J:162641
|
Clp1tm1.1Pngr/Clp1tm1.1Pngr
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:196364
|
increased cellular sensitivity to oxidative stress
|
J:196364
|
oxidative stress
|
J:196364
|
Clp1tm1.1Pngr/Clp1tm1.1Pngr
(CBA.Cg-Clp1tm1.1Pngr)
|
maternal effect
|
J:196364
|
Clp1tm1.1Pngr/Clp1tm1.1Pngr
(B6.Cg-Clp1tm1.1Pngr)
|
defasiculated phrenic nerve
|
J:196364
|
increased neuron apoptosis
|
J:209564
|
ClppGt(IST11134F10)Tigm/ClppGt(IST11134F10)Tigm
(involves: C57BL/6N)
|
abnormal cellular respiration
|
J:203140
|
abnormal oogenesis
|
J:203140
|
azoospermia
|
J:203140
|
decreased fibroblast proliferation
|
J:203140
|
disorganized mitochondrial cristae
|
J:203140
|
early cellular replicative senescence
|
J:203140
|
increased granulosa cell apoptosis
|
J:203140
|
increased mitochondrial DNA content
|
J:203140
|
increased mitochondrial size
|
J:203140
|
ClppGt(IST13563G11)Tigm/ClppGt(IST13563G11)Tigm
(involves: C57BL/6N)
|
abnormal cellular respiration
|
J:203140
|
abnormal oogenesis
|
J:203140
|
azoospermia
|
J:203140
|
decreased fibroblast proliferation
|
J:203140
|
disorganized mitochondrial cristae
|
J:203140
|
early cellular replicative senescence
|
J:203140
|
increased embryonic tissue cell apoptosis
|
J:203140
|
increased mitochondrial DNA content
|
J:203140
|
increased mitochondrial size
|
J:203140
|
Clrn1tm1.1Ugpa/Clrn1tm1.1Ugpa Myo15atm1.1(cre)Ugds/Myo15a+
(involves: 129S1/SvImJ * C57BL/6N)
|
abnormal synaptic vesicle exocytosis
|
J:265318
|
Clrn1tm1.2Ugpa/Clrn1tm1.2Ugpa
(involves: BALB/c * C57BL/6 * C57BL/6N)
|
abnormal synaptic vesicle exocytosis
|
J:265318
|
Clspntm1(KOMP)Vlcg/Clspn+
(C57BL/6N-Clspntm1(KOMP)Vlcg)
|
abnormal DNA repair
|
J:332163
|
abnormal female meiosis I arrest
|
J:332163
|
impaired polar body extrusion
|
J:332163
|
increased hepatocyte proliferation
|
J:332163
|
maternal effect
|
J:332163
|
Cltrntm1Thu/Y
(involves: 129S/SvEv * C57BL/6)
|
abnormal tricarboxylic acid cycle
|
J:148522
|
Clutm1Jakh/Clutm1Jakh
(involves: 129S2/SvPas * Black Swiss)
|
increased mesangial cell number
|
J:74983
|
Cluap1tm1.2Hmd/Cluap1tm1.2Hmd
(involves: 129S6/SvEvTac * C57BL/6NCr)
|
abnormal cilium morphology
|
J:200709
|
abnormal ependyma motile cilium physiology
|
J:200709
|
absent embryonic cilia
|
J:200709
|
decreased embryonic cilium length
|
J:200709
|
Cluap1tm1a(KOMP)Wtsi/Cluap1tm1a(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
absent embryonic cilia
|
J:196506
|
Cluhtm1.1Eir/Cluhtm1.1Eir Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: BALB/cJ * C57BL/6 * DBA * SJL)
|
abnormal cellular respiration
|
J:249661
|
abnormal hepatocyte mitochondrial morphology
|
J:249661
|
increased apoptosis
|
J:249661
|
Cluhtm1.2Eir/Cluhtm1.2Eir
(involves: BALB/cJ * C57BL/6 * SJL)
|
abnormal hepatocyte mitochondrial morphology
|
J:249661
|
abnormal mitochondrial matrix morphology
|
J:249661
|
abnormal tricarboxylic acid cycle
|
J:249661
|
cellular phenotype
|
J:249661
|
Clxntm1.1Osb/Clxntm1.1Osb
(involves: C57BL * C57BL/6NSlc * DBA)
|
abnormal brain ependyma motile cilium physiology
|
J:278278
|
abnormal motile primary cilium morphology
|
J:278278
|
abnormal motile primary cilium physiology
|
J:278278
|
abnormal respiratory motile cilium physiology
|
J:278278
|
absent embryonic cilia
|
J:278278
|
asthenozoospermia
|
J:278278
|
cellular phenotype
|
J:278278
|
decreased embryonic cilium number
|
J:278278
|
Cmahtm1Ykoz/Cmahtm1Ykoz
(B6.129P2-Cmahtm1Ykoz)
|
increased B cell proliferation
|
J:121365
|
Cmastm1.1Bwei/Cmastm1.1Bwei Tg(NPHS2-cre)295Lbh/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
increased mesangial cell number
|
J:286022
|
Cmklr1tm1Dgen/Cmklr1tm1Dgen
(B6.Cg-Cmklr1tm1Dgen)
|
abnormal macrophage chemotaxis
|
J:157190
|
Cmklr1tm1Drg/Cmklr1tm1Drg
(Not Specified)
|
impaired macrophage chemotaxis
|
J:133968
|
Cmtm2aem1Osb/Cmtm2aem1Osb Cmtm2bem1Osb/Cmtm2bem1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
immotile sperm
|
J:266476
|
Cmtm3em1Wlh/Cmtm3em1Wlh
(involves: C57BL/6)
|
abnormal myocardial fiber mitochondrial morphology
|
J:338327
|
dilated mitochondrion
|
J:338327
|
Cmtm4em1Wlh/Cmtm4em1Wlh
(involves: C57BL/6J)
|
abnormal sperm head morphology
|
J:294647
|
abnormal sperm midpiece morphology
|
J:294647
|
decreased sperm progressive motility
|
J:294647
|
oligozoospermia
|
J:294647
|
Cmtm4tm1d(EUCOMM)Wtsi/Cmtm4tm1d(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal fibroblast physiology
|
J:333836
|
Cmtm7tm2a(EUCOMM)Hmgu/Cmtm7+ Rag1tm1Fwa/Rag1tm1Fwa
(chimera involves: C57BL/6 * C57BL/6N)
|
decreased B cell proliferation
|
J:207033
|
Cmya5tm1Cap/Cmya5tm1Cap
(129-Cmya5tm1Cap)
|
cardiac interstitial fibrosis
|
J:322761
|
Cnbd2tm1Dwac/Cnbd2tm1Dwac
(B6.Cg-Cnbd2tm1Dwac)
|
abnormal motile cilium physiology
|
J:207897
|
abnormal sperm midpiece morphology
|
J:207897
|
abnormal sperm motility
|
J:207897
|
arrest of male meiosis
|
J:207897
|
azoospermia
|
J:207897
|
Cnbpm1Hrb/Cnbpm1Hrb
(B6.129S4-Cnbpm1Hrb)
|
decreased embryonic tissue cell apoptosis
|
J:81582
|
Cngb3tm1Dgen/Cngb3tm1Dgen
(involves: C57BL/6)
|
increased retina apoptosis
|
J:154304
|
Cnih4tm1a(EUCOMM)Hmgu/Cnih4tm1a(EUCOMM)Hmgu
(involves: C57BL/6N)
|
asthenozoospermia
|
J:333288
|
oligozoospermia
|
J:333288
|
teratozoospermia
|
J:333288
|
Cnmdtm1Ska/Cnmdtm1Ska
(involves: C57BL/6 * CBA)
|
abnormal osteoblast physiology
|
J:81137
|
Cnn1tm1Tkhi/Cnn1tm1Tkhi
(involves: 129S/SvEv * C57BL/6)
|
enhanced osteoblast differentiation
|
J:77112
|
Cnn2tm1.2Jin/Cnn2tm1.2Jin
(B6.129X1-Cnn2tm1.2Jin)
|
abnormal macrophage chemotaxis
|
J:141867
|
Cnot3tm1.1Tya/Cnot3+
(B6.129P2(Cg)-Cnot3tm1.1Tya)
|
abnormal osteoclast differentiation
|
J:206802
|
Cnot7tm1Jpr/Cnot7tm1Jpr
(involves: 129/Sv * C57BL/6)
|
abnormal male germ cell morphology
|
J:91598
|
decreased male germ cell number
|
J:91598
|
oligozoospermia
|
J:91598
|
Cnot7tm1Tno/Cnot7tm1Tno
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:90439
|
abnormal sperm head morphology
|
J:90439
|
abnormal sperm mitochondrial sheath morphology
|
J:90439
|
abnormal spermatid morphology
|
J:90439
|
asthenozoospermia
|
J:90439
|
decreased elongated spermatid number
|
J:90439
|
increased male germ cell apoptosis
|
J:90439
|
multinucleated giant male germ cells
|
J:90439
|
oligozoospermia
|
J:90439
|
teratozoospermia
|
J:90439
|
Cnot7tm1Tno/Cnot7tm1Tno Cnot8tm1.1Tya/Cnot8tm1.1Tya
(involves: 129S4/SvJaeSor * C57BL/6Ncrlj * CBA/JNCrlj)
|
increased fibroblast apoptosis
|
J:304598
|
Cnptm1(cre)Kan/Cnp+ Tfamtm1Lrsn/Tfamtm1Lrsn
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased mitochondrial DNA content
|
J:228933
|
decreased neuron mitochondrial DNA content
|
J:228933
|
Cnpy2tm1.2Zhli/Cnpy2tm1.2Zhli
(B6.Cg-Cnpy2tm1.2Zhli)
|
decreased endoplasmic reticulum stress
|
J:277868
|
decreased sensitivity to induced cell death
|
J:277868
|
Cnr1tm1.1Ltz/Cnr1tm1.1Ltz
(B6.129P2-Cnr1tm1.1Ltz)
|
abnormal axon fasciculation
|
J:171771
|
Cnr1tm1.2Ltz/Cnr1tm1.2Ltz Neurod6tm1(cre)Kan/Neurod6+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6NCrl)
|
abnormal axon fasciculation
|
J:171771
|
Cnr1tm1.2Ltz/Cnr1tm1.2Ltz Tg(Camk2a-cre)2Gsc/0
(involves: 129P2/OlaHsd * C57BL/6N)
|
increased susceptibility to neuronal excitotoxicity
|
J:89842
|
Cnr1tm1Map/Cnr1tm1Map
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal neuronal precursor proliferation
|
J:102006
|
increased susceptibility to neuronal excitotoxicity
|
J:109213
|
Cnr1tm1Map/Cnr1tm1Map
(involves: 129S1/Sv * 129X1/SvJ)
|
increased sperm motility
|
J:123226
|
Cnr1tm1Zim/Cnr1tm1Zim
(involves: 129 * C57BL/6J)
|
maternal effect
|
J:144423
|
Cntd1em1Atot/Cntd1em1Atot
(either: (involves: C57BL/6JCrl) or (involves: CD-1))
|
abnormal meiosis
|
J:292293
|
Cntd1em2Atot/Cntd1em2Atot
(either: (involves: C57BL/6JCrl) or (involves: CD-1))
|
abnormal meiosis
|
J:292293
|
Cntd1tm1e.1(KOMP)Wtsi/Cntd1tm1e.1(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal female meiosis
|
J:215796
|
abnormal male meiosis
|
J:215796
|
abnormal spermatocyte morphology
|
J:215796
|
azoospermia
|
J:215796
|
decreased spermatid number
|
J:215796
|
Cntftm1Mpin/Cntftm1Mpin
(B6.129S2-Cntftm1Mpin)
|
abnormal oligodendrocyte apoptosis
|
J:126852
|
decreased oligodendrocyte progenitor number
|
J:126852
|
Cntftm1Mpin/Cntftm1Mpin
(involves: 129S2/SvPas * C57BL/6)
|
abnormal axon extension
|
J:158286
|
Cntftm1Mpin/Cntftm1Mpin Liftm1Phb/Liftm1Phb
(involves: 129S2/SvPas * C57BL/6)
|
abnormal axon extension
|
J:158286
|
Cntftm1Vlcg/Cntftm1Vlcg
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
abnormal neuron proliferation
|
J:186611
|
Cntlnem1Wli/Cntlnem1Wli
(involves: C57BL/6J * DBA/2J)
|
absent sperm head
|
J:324173
|
Cntn1tm1Brns/Cntn1tm1Brns
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6)
|
abnormal axon fasciculation
|
J:58556
|
abnormal axon guidance
|
J:58556
|
Cntnap2tm1Pele/Cntnap2tm1Pele
(B6.129-Cntnap2tm1Pele)
|
abnormal neuronal migration
|
J:177110
|
Cntnap4em1Smoc/Cntnap4em1Smoc
(C57BL/6J-Cntnap4em1Smoc)
|
enhanced autophagy
|
J:287186
|
Coa8em1Zev/Coa8em1Zev
(FVB/NJ-Coa8em1Zev)
|
abnormal respiratory electron transport chain
|
J:277865
|
Coasytm1.1Vtr/Coasytm1.1Vtr Tg(Syn1-cre)671Jxm/0
(involves: 129 * C57BL/6N * CBA)
|
abnormal mitochondrial physiology
|
J:299154
|
Cobltm1.1Bqu/Cobltm1.1Bqu
(B6.129(Cg)-Cobltm1.1Bqu)
|
abnormal outer hair cell kinocilium morphology
|
J:271615
|
abnormal pericentriolar material morphology
|
J:271615
|
Coiltm1Agm/Coiltm1Agm
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J))
|
abnormal Cajal body morphology
|
J:70593
|
Col1a1Aga2/Col1a1+
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal osteoblast physiology
|
J:129569
|
increased osteoblast apoptosis
|
J:129569
|
Col1a1Aga2/Col1a1+
(C3HeB/FeJ-Col1a1Aga2)
|
abnormal cell morphology
|
J:185988
|
abnormal endoplasmic reticulum morphology
|
J:185988
|
abnormal Golgi apparatus morphology
|
J:185988
|
Col1a1em1Nju/Col1a1+
(C57BL/6-Col1a1em1Nju)
|
impaired osteoblast differentiation
|
J:358220
|
Col1a1M1Jrt/Col1a1+
(involves: C3H/HeJ * C57BL/6J * FVB/NJ)
|
abnormal extracellular matrix morphology
|
J:216423
|
Col1a1tm1(tetO-CDKN2A)Ibp/Col1a1+ Tg(KRT5-rtTA)#Glk/0
(involves: 129S4/SvJae * C57BL/6 * FVB)
|
early cellular replicative senescence
|
J:196969
|
Col1a1tm1(tetO-CDKN2A)Ibp/Col1a1tm2(tetO-GFP/RNAi:Trp53)Slowe Tg(KRT5-rtTA)#Glk/0
(involves: 129S4/SvJae * C57BL/6 * FVB)
|
cellular phenotype
|
J:196969
|
Col1a1tm1(tetO-cre)Haho/? Gfi1btm1.1Haho/Gfi1btm1.1Haho
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:207446
|
Col1a1tm1(tetO-CTNNB1)Tcd/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J)
|
abnormal enterocyte apoptosis
|
J:193365
|
abnormal enterocyte proliferation
|
J:193365
|
increased enterocyte apoptosis
|
J:193365
|
Col1a1tm1(tetO-EWSR1/ATF1)Yasu/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
decreased fibroblast proliferation
|
J:194505
|
Col1a1tm1(tetO-Fos)Wag/Col1a1+ Tg(KRT5-rtTA)T2D6Sgkd/0
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
increased keratinocyte proliferation
|
J:201145
|
Col1a1tm1(tetO-Lin28a)Gqda/Col1a1+
(involves: 129S4/SvJae * C57BL/6 * CD-1)
|
increased cell proliferation
|
J:166568
|
increased hepatocyte proliferation
|
J:166568
|
Col1a1tm1(tetO-SOX2)Mjm/Col1a1+ Gt(ROSA)26Sortm1(tTA)Roos/Gt(ROSA)26Sor+ Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2J)
|
increased cell proliferation
|
J:199754
|
Col1a1tm1(tetO-Tcfap2c)Hsc/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal enterocyte proliferation
|
J:174049
|
abnormal hepatocyte mitochondrial morphology
|
J:174049
|
increased hepatocyte apoptosis
|
J:174049
|
increased hepatocyte proliferation
|
J:174049
|
Col1a1tm1(tetO-URI1)Ndj/Col1a1+ Tg(Cebpb-tTA)#Bjd/0 Trp53tm1Gev/Trp53+
(B6.Cg-Trp53tm1Gev Col1a1tm1(tetO-URI1)Ndj Tg(Cebpb-tTA)#Bjd)
|
decreased hepatocyte apoptosis
|
J:217463
|
Col1a1tm1(tetO-YAP1*)Fcam/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal enterocyte proliferation
|
J:141457
|
abnormal intestinal goblet cell morphology
|
J:141457
|
increased cell proliferation
|
J:141457
|
Col1a1tm1(tetO-YAP1*)Fcam/Col1a1+ Gt(ROSA)26Sortm1(rtTA,EGFP)Nagy/Gt(ROSA)26Sor+ Tg(KRT14-cre)1Amc/0
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * CBA)
|
increased cell proliferation
|
J:171057
|
Col1a1tm1(tetO-YAP1*)Fcam/Col1a1+ Tg(Cebpb-tTA)#Bjd/0
(involves: 129S4/SvJae * C57BL/6)
|
decreased hepatocyte apoptosis
|
J:141457
|
increased hepatocyte proliferation
|
J:141457
|
Col1a1tm1Jae/Col1a1tm1Jae
(involves: 129S4/SvJae * C57BL/6)
|
abnormal osteoblast differentiation
|
J:85591,
J:90884
|
increased osteoblast apoptosis
|
J:90884
|
increased osteocyte apoptosis
|
J:90884
|
Col1a1tm2(CAG-IDH2*R172K)Kkw/Col1a1+ Ndor1Tg(UBC-cre/ERT2)1Ejb/0
(involves: 129S/SvEv * 129S4/SvJae * BALB/c * C57BL/6)
|
abnormal mitochondrial crista morphology
|
J:209629
|
abnormal mitochondrial morphology
|
J:209629
|
abnormal mitochondrial physiology
|
J:209629
|
abnormal myocardial fiber mitochondrial morphology
|
J:209629
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:209629
|
decreased mitochondrial number
|
J:209629
|
increased cardiomyocyte apoptosis
|
J:209629
|
Col1a1tm2(tetO-CTNNB1*)Hoch/Col1a1tm2(tetO-CTNNB1*)Hoch Gt(ROSA)26Sortm1(rtTA*M2)Jae/?
(involves: 129S4/SvJae * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:191050
|
Col1a1tm2(tetO-Fosl2,-DsRed)Wag/Col1a1+ Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
(involves: 129S4/SvJae * C57BL/6 * CD-1)
|
abnormal osteoblast physiology
|
J:211215
|
Col1a1tm2(tetO-IDH2*R140Q)Ppp/Col1a1tm2(tetO-IDH2*R140Q)Ppp Gt(ROSA)26Sortm1(rtTA*M2)Jae/?
(involves: 129S4/SvJae * C57BL/6)
|
abnormal hematopoietic stem cell proliferation
|
J:210097
|
increased hematopoietic stem cell proliferation
|
J:210097
|
Col1a1tm2(tetO-Pou5f1)Jae/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell proliferation
|
J:98920
|
Col1a1tm2(tetO-Pou5f1)Jae/Col1a1+ Gt(ROSA)26Sortm1(tTA)Roos/Gt(ROSA)26Sor+ Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2J)
|
increased cell proliferation
|
J:199754
|
Col1a1tm3(CAG-IDH2*R140Q)Kkw/Col1a1+ Ndor1Tg(UBC-cre/ERT2)1Ejb/0
(involves: 129S/SvEv * 129S4/SvJae * BALB/c * C57BL/6)
|
abnormal mitochondrial crista morphology
|
J:209629
|
abnormal mitochondrial morphology
|
J:209629
|
abnormal mitochondrial physiology
|
J:209629
|
abnormal myocardial fiber mitochondrial morphology
|
J:209629
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:209629
|
decreased mitochondrial number
|
J:209629
|
increased cardiomyocyte apoptosis
|
J:209629
|
Col1a1tm3(tetO-Mirlet7g/Mir21)Gqda/? Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
decreased primordial germ cell number
|
J:196313
|
Col1a1tm8(tetO-GFP/RNAi:Rpa3)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+ Tg(CMV-rtTA)4Bjd/0
(involves: 129S4/SvJae * C57BL/6 * NMRI)
|
abnormal cell cycle
|
J:171348
|
Col1a1tm8(tetO-GFP/RNAi:Rpa3)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:171348
|
Col1a1tm8(tetO-GFP/RNAi:Rpa3)Slowe/Col1a1+ Tg(CMV-rtTA)4Bjd/0
(involves: 129S4/SvJae * C57BL/6 * NMRI)
|
abnormal cell cycle
|
J:171348
|
Col1a1tm10(tetO*-RFP/RNAi:Rpa3)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:171348
|
early cellular replicative senescence
|
J:171348
|
Col1a1tm10(tetO*-RFP/RNAi:Rpa3)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae
(involves: 129S4/SvJae * C57BL/6)
|
abnormal small intestinal crypt cell proliferation
|
J:171348
|
Col1a1tm11(tetO*-RFP/RNAi:Rpa3)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:171348
|
early cellular replicative senescence
|
J:171348
|
Col1a1tm11(tetO*-RFP/RNAi:Rpa3)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sortm1(rtTA*M2)Jae
(involves: 129S4/SvJae * C57BL/6)
|
abnormal small intestinal crypt cell proliferation
|
J:171348
|
Col1a1tm11(tetO-Nup88)Jvd/Col1a1+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:231166
|
abnormal mitosis
|
J:231166
|
abnormal mitotic spindle morphology
|
J:231166
|
aneuploidy
|
J:231166
|
chromosomal instability
|
J:231166
|
Col1a1tm13(tetO-Nup88)Jvd/Col1a1+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:231166
|
abnormal mitosis
|
J:231166
|
abnormal mitotic spindle morphology
|
J:231166
|
aneuploidy
|
J:231166
|
chromosomal instability
|
J:231166
|
Col1a1tm17(tetO-GFP,-cas9*)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal small intestinal crypt cell proliferation
|
J:222595
|
Col1a1tm19(tetO-GFP,-cas9*)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal small intestinal crypt cell proliferation
|
J:222595
|
Col1a1tm20(tetO-GFP,-cas9*D10A)Slowe/Col1a1+ Gt(ROSA)26Sortm1(rtTA*M2)Jae/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal small intestinal crypt cell proliferation
|
J:222595
|
Col1a2oim/Col1a2oim
(B6C3Fe a/a-Col1a2oim/J)
|
cellular phenotype
|
J:124000
|
Col2a1Rgsc413/Col2a1Rgsc413
(involves: C57BL/6JJcl * DBA/2JJcl)
|
increased chondrocyte apoptosis
|
J:260538
|
Col2a1tm1(SOX9)Crm/Col2a1+
(129S/Sv-Col2a1tm1(SOX9)Crm)
|
decreased chondrocyte proliferation
|
J:90567
|
Col3a1Tsk2/Col3a1+
(C3H101H-Col3a1Tsk2/H)
|
cellular phenotype
|
J:55591
|
Col4a1deltaex40/Col4a1+
(B6.129S-Col4a1deltaex40)
|
abnormal basement membrane morphology
|
J:215446
|
Col4a3tm1Dec/Col4a3tm1Dec
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cochlear basement membrane morphology
|
J:91619
|
increased mesangial cell number
|
J:37963
|
Col4a3tm1Dec/Col4a3tm1Dec
(129X1/SvJ-Col4a3tm1Dec)
|
abnormal cochlear basement membrane morphology
|
J:91619,
J:98449
|
Col4a5tm1Yseg/Y
(B6.Cg-Col4a5tm1Yseg)
|
increased mesangial cell number
|
J:102306
|
Col5a3tm1Dgr/Col5a3tm1Dgr
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
decreased adipocyte glucose uptake
|
J:171817
|
decreased skeletal muscle cell glucose uptake
|
J:171817
|
increased pancreatic beta cell apoptosis
|
J:171817
|
increased pancreatic islet cell apoptosis
|
J:171817
|
Col6a3tm2.1Chu/Col6a3+
(B6.129(Cg)-Col6a3tm2.1Chu)
|
abnormal mitochondrial shape
|
J:208903
|
Col6a3tm2.1Chu/Col6a3tm2.1Chu
(B6.129(Cg)-Col6a3tm2.1Chu)
|
abnormal mitochondrial shape
|
J:208903
|
Col8a2tm1.1Asj/Col8a2tm1.1Asj
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal endoplasmic reticulum morphology
|
J:179022
|
abnormal mitochondrial morphology
|
J:179022
|
increased apoptosis
|
J:179022
|
Col8a2tm1.1Asj/Col8a2tm1.1Asj
(involves: 129S6/SvEvTac)
|
abnormal autophagy
|
J:214908
|
abnormal endoplasmic reticulum morphology
|
J:214908
|
Col8a2tm2.1Asj/Col8a2tm2.1Asj
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal autophagy
|
J:214908
|
abnormal endoplasmic reticulum morphology
|
J:214908
|
Col9a1tm1Jae/Col9a1tm1Jae
(either: (involves: 129S2/SvPas * BALB/c) or (involves: 129S2/SvPas * C57BL))
|
increased chondrocyte proliferation
|
J:18628
|
Col10a1tm1.1Rpbh/Col10a1tm1.1Rpbh
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell morphology
|
J:154052
|
increased endoplasmic reticulum stress
|
J:154052
|
Col10a1tm2.1Rpbh/Col10a1+
(involves: C57BL/6NTac)
|
increased endoplasmic reticulum stress
|
J:267200
|
Col10a1tm2.1Rpbh/Col10a1tm2.1Rpbh
(involves: C57BL/6NTac)
|
increased endoplasmic reticulum stress
|
J:267200
|
Col12a1tm1Debi/Col12a1tm1Debi
(involves: 129 * C57BL/6)
|
abnormal actin cytoskeleton morphology
|
J:174217
|
abnormal osteoblast physiology
|
J:174217
|
Col13a1tm1Pih/Col13a1tm1Pih
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J))
|
abnormal basement membrane morphology
|
J:71939
|
abnormal cell adhesion
|
J:71939
|
Col13a1tm3.1Pih/Col13a1tm3.1Pih
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal endocytosis
|
J:242846
|
Col13a1tm4.1Pih/Col13a1tm4.1Pih
(involves: C57BL/6)
|
abnormal endocytosis
|
J:242846
|
abnormal synaptic vesicle exocytosis
|
J:242846
|
Col17a1tm1.1(COL17A1)Zliu/Col17a1tm1.1(COL17A1)Zliu
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased mast cell degranulation
|
J:261781
|
Col17a1tm1Tiin/Col17a1tm1Tiin
(involves: C57BL/6)
|
abnormal basement membrane morphology
|
J:220622
|
increased fibroblast proliferation
|
J:220622
|
Col18a1tm1Hms/Col18a1tm1Hms
(either: (involves: 129S4/SvJae * 129X1/SvJ) or (involves: 129S4/SvJae * C57BL/6J))
|
abnormal basement membrane morphology
|
J:75861
|
Col18a1tm1Hms/Col18a1tm1Hms
(involves: 129S4/SvJae * C57BL/6J * C57BL/6JOlaHsd)
|
abnormal basement membrane morphology
|
J:92842
|
abnormal brain ependyma motile cilium morphology
|
J:92842
|
Col25a1tm1.1Tiwa/Col25a1tm1.1Tiwa Tg(Hlxb9-GFP)1Tmj/0
(B6.Cg-Col25a1tm1.1Tiwa Tg(Hlxb9-GFP)1Tmj)
|
increased neuron apoptosis
|
J:206855
|
Colgalt1tm1.1Gpt/Colgalt1tm1.1Gpt
(Not Specified)
|
decreased hepatocyte proliferation
|
J:283330
|
Colgalt2tm1.1Hwei/Colgalt2tm1.1Hwei
(involves: C57BL/6J)
|
increased T cell apoptosis
|
J:310468
|
Comptm1Mbri/Comp+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased chondrocyte proliferation
|
J:125086
|
increased chondrocyte apoptosis
|
J:125086
|
Comptm1Mbri/Comptm1Mbri
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased chondrocyte proliferation
|
J:125086
|
increased chondrocyte apoptosis
|
J:125086
|
Copb2em1Rstot/Copb2em2Rstot
(involves: C57BL/6 * C57BL/6J * CD-1 * DBA/2)
|
abnormal neuron proliferation
|
J:252710
|
increased neuron apoptosis
|
J:252710
|
increased neuronal precursor proliferation
|
J:252710
|
Copg1em1Geha/Copg1em1Geha
(involves: C57BL/6)
|
abnormal endoplasmic reticulum morphology
|
J:345528
|
increased endoplasmic reticulum stress
|
J:345528
|
increased T cell apoptosis
|
J:345528
|
Coprstm1.1Efab/Coprstm1.1Efab
(Not Specified)
|
abnormal fat cell differentiation
|
J:221154
|
Cops2tm1Nwe/Cops2tm1Nwe
(involves: 129 * C57BL/6J)
|
absent inner cell mass proliferation
|
J:85761
|
Cops5tm1Fxc/Cops5+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
decreased cell proliferation
|
J:166561
|
Cops5tm1Fxc/Cops5tm1Fxc
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal DNA repair
|
J:166561
|
abnormal inner cell mass apoptosis
|
J:166561
|
decreased inner cell mass proliferation
|
J:166561
|
increased embryonic tissue cell apoptosis
|
J:166561
|
spontaneous chromosome breakage
|
J:166561
|
Cops5tm1Jka/Cops5tm1Jka
(involves: 129S4/SvJae * C57BL/6)
|
abnormal trophoblast giant cell proliferation
|
J:93979
|
absent inner cell mass proliferation
|
J:93979
|
Cops5tm1Rpar/Cops5tm1Rpar Tg(Lck-cre)548Jxm/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL)
|
abnormal cell cycle checkpoint function
|
J:132114
|
increased T cell apoptosis
|
J:132114
|
Cops5tm1Rpar/Cops5tm1Rpar Tg(Stra8-icre)1Reb/0
(involves: 129 * C57BL/6 * FVB/NJ * SJL)
|
abnormal acrosome assembly
|
J:307573
|
abnormal sperm nucleus morphology
|
J:307573
|
abnormal spermatid morphology
|
J:307573
|
asthenozoospermia
|
J:307573
|
decreased elongated spermatid number
|
J:307573
|
immotile sperm
|
J:307573
|
increased male germ cell apoptosis
|
J:307573
|
oligozoospermia
|
J:307573
|
teratozoospermia
|
J:307573
|
Cops6Gt(RRI087)Byg/Cops6+
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased cellular sensitivity to gamma-irradiation
|
J:172038
|
increased sensitivity to induced cell death
|
J:172038
|
increased thymocyte apoptosis
|
J:172038
|
Cops8tm1.1Nwe/Cops8tm1.1Nwe
(involves: C57BL/6)
|
abnormal inner cell mass proliferation
|
J:126339
|
Cops8tm1Nwe/Cops8tm1.1Nwe
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell cycle
|
J:126339
|
Cops8tm1Nwe/Cops8tm1.1Nwe Tg(Cd4-cre)1Cwi/?
(involves: 129S1/Sv * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:126339
|
Coq3tm1Hek/Coq3+
(129S/SvEv-Coq3tm1Hek)
|
cellular phenotype
|
J:278535
|
Coq6em1Shcm/Coq6em1Shcm
(C57BL/6-Coq6em1Shcm)
|
abnormal oxidative phosphorylation
|
J:360514
|
abnormal respiratory electron transport chain
|
J:360514
|
Coq6tm1c(EUCOMM)Hmgu/Coq6tm1c(EUCOMM)Hmgu Tg(NPHS2-cre)295Lbh/0
(involves: C57BL/6 * C57BL/6N * SJL)
|
abnormal mitochondrial physiology
|
J:278754
|
increased mitochondrial number
|
J:278754
|
increased mitochondrial size
|
J:278754
|
Coq7tm1Hek/Coq7+
(involves: 129S1/Sv * 129X1/SvJ * BALB/c)
|
abnormal mitochondrial physiology
|
J:278535
|
Coq7tm1Hek/Coq7tm2Hek Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
abnormal respiratory electron transport chain
|
J:202240
|
Coq7tm1Tsh/Coq7tm1Tsh
(involves: C57BL/6)
|
abnormal aerobic respiration
|
J:73111
|
abnormal lysosome morphology
|
J:73111
|
abnormal mitochondrial morphology
|
J:73111
|
decreased cell proliferation
|
J:73111
|
Coq7tm2Hek/Coq7tm2Hek
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
abnormal respiratory electron transport chain
|
J:202240
|
cellular phenotype
|
J:202240
|
increased cell death
|
J:202240
|
Coq8btm1c(EUCOMM)Hmgu/Coq8btm1c(EUCOMM)Hmgu Tg(NPHS2-cre)295Lbh/0
(involves: C3H * C57BL/6 * C57BL/6N * SJL)
|
increased mitochondrial number
|
J:294296
|
increased mitochondrial size
|
J:294296
|
Coq9tm1.1Lcl/Coq9tm1.1Lcl
(involves: C57BL/6 * C57BL/6NTac * SJL)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:193288
|
abnormal mitochondrial physiology
|
J:193288
|
increased neuron apoptosis
|
J:193288
|
oxidative stress
|
J:193288
|
Coro1aptcd/Coro1aptcd
(B6.CTS-Coro1aptcd)
|
increased T cell apoptosis
|
J:141431
|
Coro1atm1Achn/Coro1atm1Achn
(involves: 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:111593
|
Coro1atm1Achn/Coro1atm1Achn
(B6.129X1-Coro1atm1Achn)
|
increased T cell apoptosis
|
J:141431
|
Coro1atm1Achn/Coro1atm1Achn
(involves: 129X1/SvJ)
|
increased mast cell degranulation
|
J:177785
|
Coro1atm1Achn/Coro1atm1Achn Coro1btm1.1Nfoe/Coro1btm1.1Nfoe
(involves: 129X1/SvJ * C57BL/6N)
|
increased mast cell degranulation
|
J:177785
|
Coro1atm1Jpie/Coro1atm1Jpie
(involves: 129 * C57BL/6)
|
decreased T cell proliferation
|
J:133258
|
impaired macrophage phagocytosis
|
J:133404
|
Coro2btm1(KOMP)Wtsi/Coro2btm1(KOMP)Wtsi
(C57BL/6-Coro2btm1(KOMP)Wtsi)
|
abnormal cell adhesion
|
J:254431
|
Coro7tm1a(EUCOMM)Hmgu/Coro7tm1a(EUCOMM)Hmgu
(C57BL/6N-Coro7tm1a(EUCOMM)Hmgu)
|
abnormal actin cytoskeleton morphology
|
J:235774
|
abnormal cell adhesion
|
J:235774
|
abnormal Golgi apparatus morphology
|
J:235774
|
increased fibroblast cell migration
|
J:235774
|
Cox6b2em1Osb/Cox6b2em1Osb
(B6;D2-Cox6b2em1Osb/Osb)
|
asthenozoospermia
|
J:345850
|
cellular phenotype
|
J:345850
|
decreased sperm progressive motility
|
J:345850
|
Cox7a1tm1Hutt/Cox7a1tm1Hutt
(B6.129-Cox7a1tm1Hutt)
|
abnormal cellular respiration
|
J:192141
|
Cox7a2lGt(OST241316)Lex/Cox7a2lGt(OST241316)Lex
(B6.129S5-Cox7a2lGt(OST241316)Lex)
|
abnormal cellular respiration
|
J:215964
|
abnormal oxidative phosphorylation
|
J:215964
|
Cox7a2ls/Cox7a2ls
(C57BL/6JCrl)
|
abnormal respiratory electron transport chain
|
J:199458
|
Cox7b2em1Smtb/Cox7b2em1Smtb
(C57BL/6NSlc-Cox7b2em1Smtb/Smtb)
|
abnormal sperm head morphology
|
J:308859
|
abnormal sperm midpiece morphology
|
J:308859
|
abnormal sperm mitochondrial sheath morphology
|
J:308859
|
asthenozoospermia
|
J:308859
|
teratozoospermia
|
J:308859
|
Cox8cem1Osb/Cox8cem1Osb
(B6;D2-Cox8cem1Osb/Osb)
|
cellular phenotype
|
J:345850
|
Cox10tm1Ctm/Cox10tm1Ctm Tg(Camk2a-cre)#Szi/0
(involves: 129X1/SvJ * C57BL/6 * C57BL/6J * CBA)
|
abnormal mitochondrial physiology
|
J:188773
|
Cox15tm1.1Zev/Cox15tm1.1Zev Tg(ACTA1-cre)79Jme/0
(involves: 129 * C57BL/6 * C57BL/6J * SJL)
|
abnormal cellular respiration
|
J:176080
|
abnormal muscle fiber mitochondrial morphology
|
J:176080
|
increased mitochondrial fission
|
J:176080
|
Cox17tm1Kako/Cox17tm1Kako
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:79609
|
Cptm1Samd/Cptm1Samd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased cellular sensitivity to hydrogen peroxide
|
J:78092
|
Cpa3tm3(icre)Hrr/Cpa3+ Fgfr1tm1Upir/Fgfr1tm1Upir Fgfr2tm1Dor/Fgfr2tm1Dor Tg(KRT5-cre)5132Jlj/0
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * C57BL/6J * DBA/2J)
|
increased keratinocyte proliferation
|
J:221184
|
Cpa3tm3(icre)Hrr/Cpa3+ Gt(ROSA)26Sortm1Hjf/? Notch1tm1Agt/Notch1tm1Agt
(involves: 129 * C57BL/6)
|
abnormal dendritic cell differentiation
|
J:143731
|
Cpaptm1a(EUCOMM)Wtsi/Cpaptm1a(EUCOMM)Wtsi
(B6Brd;B6N-Tyrc-Brd Cpaptm1a(EUCOMM)Wtsi/Wtsi)
|
abnormal cell physiology
|
J:194085
|
abnormal double-strand DNA break repair
|
J:194085
|
abnormal mitosis
|
J:194085
|
abnormal mitotic spindle morphology
|
J:194085
|
cellular phenotype
|
J:194085
|
chromosomal instability
|
J:194085
|
increased embryonic tissue cell apoptosis
|
J:194085
|
retention of the adrenal gland x-zone
|
J:194085
|
Cpaptm1d(EUCOMM)Wtsi/Cpaptm1d(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N * FVB/NJ)
|
abnormal centrosome morphology
|
J:208632
|
abnormal mitosis
|
J:208632
|
absent embryonic cilia
|
J:208632
|
increased embryonic tissue cell apoptosis
|
J:208632
|
Cpaptm1d(EUCOMM)Wtsi/Cpaptm1d(EUCOMM)Wtsi Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6 * C57BL/6N * FVB/NJ)
|
abnormal apoptosis
|
J:208632
|
abnormal centrosome morphology
|
J:208632
|
abnormal mitosis
|
J:208632
|
Cpeb1tm1Rcht/Cpeb1tm1Rcht
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal female meiosis
|
J:102097
|
arrest of male meiosis
|
J:102097
|
increased male germ cell apoptosis
|
J:102097
|
oligozoospermia
|
J:102097
|
Cpeb3em1Gaoxu/Cpeb3em1Gaoxu
(C57BL/6J-Cpeb3em1Gaoxu)
|
decreased granulosa cell proliferation
|
J:323073
|
increased granulosa cell apoptosis
|
J:323073
|
oocyte degeneration
|
J:323073
|
Cpeb4tm1a(EUCOMM)Wtsi/Cpeb4tm1a(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal axon extension
|
J:236098
|
abnormal cell physiology
|
J:236098
|
Cplane1b2b012Clo/Cplane1b2b012Clo
(C57BL/6J-Cplane1b2b012Clo)
|
abnormal nonmotile primary cilium morphology
|
J:223340
|
abnormal primary cilium morphology
|
J:223340
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:223340
|
Cplx1tm2Bros/Cplx1tm2Bros
(Not Specified)
|
asthenozoospermia
|
J:145652
|
Cpne7tm1Parkj/Cpne7tm1Parkj
(involves: 129S6/SvEvTac * C57BL/6N)
|
early cellular replicative senescence
|
J:347866
|
Cpsf6em1Bcgen/Cpsf6+
(Not Specified)
|
azoospermia
|
J:346988
|
Cpt1atm1.1Pec/Cpt1atm1.1Pec Tg(Cdh5-cre/ERT2)1Rha/0
(Not Specified)
|
decreased vascular endothelial cell proliferation
|
J:220527
|
Cpt1ctm1Dhwu/Cpt1ctm1Dhwu
(involves: 129 * C57BL/6J)
|
decreased skeletal muscle cell glucose uptake
|
J:148205
|
Craddtm1Mak/Craddtm1Mak
(involves: 129 * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:101402
|
Crattm1.1Pbrc/Crattm1.1Pbrc Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6J * FVB)
|
abnormal aerobic respiration
|
J:184778
|
abnormal cellular respiration
|
J:184778
|
abnormal tricarboxylic acid cycle
|
J:184778
|
Crb1tm1Wij/Crb1+ Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL)
|
decreased retina apoptosis
|
J:207895
|
increased retina apoptosis
|
J:207895
|
Crb1tm1Wij/Crb1tm1Wij Crb2tm1.1Wij/Crb2tm1.1Wij Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL)
|
increased retina apoptosis
|
J:207895
|
Crb3tm1.2Bmar/Crb3tm1.2Bmar
(B6.129(Cg)-Crb3tm1.2Bmar)
|
abnormal respiratory motile cilium morphology
|
J:206750
|
Creb1tm1.1Berd/Creb1tm1.1Berd
(B6NHsd.129S4-Creb1tm1.1Berd)
|
increased myoblast proliferation
|
J:177923
|
Creb1tm3Gsc/Creb1+ Gprc6atm1.1Kry/Gprc6a+ Tg(Cyp17a1-icre)AJako/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
oligozoospermia
|
J:170888
|
Creb1tm3Gsc/Creb1tm3Gsc Cremtm1Gsc/Cremtm1Gsc Tg(Dbh-icre)1Gsc/0
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased neuron apoptosis
|
J:121244
|
Creb1tm3Gsc/Creb1tm3Gsc Tg(Cyp17a1-icre)AJako/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
oligozoospermia
|
J:170888
|
Creb3l1tm1Kaim/Creb3l1tm1Kaim
(involves: 129S2/SvPas * C57BL/6)
|
abnormal osteoblast differentiation
|
J:158242
|
Creb3l4tm1Imad/Creb3l4tm1Imad
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
multinucleated giant male germ cells
|
J:100527
|
oligozoospermia
|
J:100527
|
Creb3l4tm1Noj/Creb3l4tm1Noj
(involves: 129S2/SvPas * C57BL/6)
|
abnormal spermatid morphology
|
J:123396
|
decreased male germ cell number
|
J:123396
|
CrebbpGt(U-San)112Imeg/Crebbp+
(involves: C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:75361
|
Crebbptm1Dli/Crebbp+
(involves: 129S6/SvEvTac * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:191503
|
Creg1tm1Yal/Creg1+
(involves: 129 * C57BL/6)
|
abnormal autophagy
|
J:253911
|
increased cardiomyocyte apoptosis
|
J:253911
|
Creld1tm1.1Chlm/Creld1tm1.1Chlm
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
increased embryonic tissue cell apoptosis
|
J:243757
|
Creld1tm1c(EUCOMM)Wtsi/Creld1tm1c(EUCOMM)Wtsi Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6 * C57BL/6N * FVB/N * SJL)
|
abnormal extracellular matrix morphology
|
J:304446
|
Creld2tm1.1Emass/Creld2tm1.1Emass
(B6.129P2(SJL)-Creld2tm1.1Emass)
|
increased endoplasmic reticulum stress
|
J:316411
|
increased hepatocyte apoptosis
|
J:316411
|
Cremtm1Gsc/Cremtm1Gsc
(involves: 129 * C57BL/6)
|
arrest of male meiosis
|
J:31889
|
Cremtm1Saco/Crem+
(involves: 129/Sv * C57BL/6)
|
oligozoospermia
|
J:31889
|
teratozoospermia
|
J:31889
|
Cremtm1Saco/Cremtm1Saco
(involves: 129/Sv * C57BL/6)
|
multinucleated giant male germ cells
|
J:81370
|
Crhtm1Maj/Crhtm1Maj
(involves: 129S2/SvPas * C57BL/6J)
|
maternal effect
|
J:23082
|
Crhtm1Maj/Crhtm1Maj
(involves: 129S2/SvPas * C57BL/6)
|
decreased T cell proliferation
|
J:98419
|
increased mesenchymal cell proliferation involved in lung development
|
J:53721
|
Crhtm2.2Maj/Crhtm2.2Maj
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
maternal effect
|
J:238330
|
Crim1Gt(KST264)Byg/Crim1Gt(KST264)Byg
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
abnormal basal lamina morphology
|
J:172334
|
increased kidney apoptosis
|
J:187026
|
Criptotm1Eda/Criptotm1Eda
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * Black Swiss) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal cell adhesion
|
J:51595
|
decreased fibroblast proliferation
|
J:51595
|
Crisp2tm1a(KOMP)Mbp/Crisp2tm1a(KOMP)Mbp
(C57BL/6N-Crisp2tm1a(KOMP)Mbp)
|
abnormal sperm motility
|
J:273472
|
asthenozoospermia
|
J:273472
|
decreased sperm progressive motility
|
J:273472
|
Crisp2tm1c(KOMP)Mbp/Crisp2tm1c(KOMP)Mbp Tg(Stra8-icre)1Reb/0
(involves: C57BL/6N * FVB/NJ)
|
asthenozoospermia
|
J:273472
|
decreased sperm progressive motility
|
J:273472
|
Crlf2tm1Wjl/Crlf2tm1Wjl
(involves: BALB/c)
|
abnormal T cell proliferation
|
J:107431
|
decreased splenocyte proliferation
|
J:107431
|
Crls1tm1Geno/Crls1tm1Geno Tg(Adipoq-cre)1Evdr/0
(involves: C57BL/6 * FVB/NJ)
|
abnormal respiratory electron transport chain
|
J:266083
|
decreased adipocyte glucose uptake
|
J:266083
|
decreased fat cell mitochondrial DNA content
|
J:266083
|
decreased mitochondrial size
|
J:266083
|
disorganized mitochondrial cristae
|
J:266083
|
Crls1tm1Geno/Crls1tm1Geno Tg(Ucp1-cre/ERT2)426Biat/0
(involves: C57BL/6N)
|
decreased mitochondrial size
|
J:266083
|
Crmp1tm1Pako/Crmp1tm1Pako
(involves: 129/Sv * ICR)
|
abnormal neuronal precursor proliferation
|
J:119127
|
impaired neuronal migration
|
J:119127,
J:116689
|
Crppam1Ddg/Crppam1Ddg
(involves: C3H/He * C57BL/6)
|
abnormal axon fasciculation
|
J:194150
|
abnormal axon guidance
|
J:194150
|
abnormal basement membrane morphology
|
J:194150
|
radial glial endfoot detachment
|
J:194150
|
crsp/crsp
(FVB/N-crsp)
|
azoospermia
|
J:69948
|
Crtac1tm1Kota/Crtac1tm1Kota
(involves: C57BL/6)
|
abnormal axon fasciculation
|
J:174418
|
Crtamtm1Achn/Crtamtm1Achn
(involves: 129 * C57BL/6)
|
increased T cell proliferation
|
J:145314
|
Crtaptm1Brle/Crtaptm1Brle
(involves: 129S7/SvEvBrd)
|
abnormal osteoblast physiology
|
J:116096
|
Crtc2tm1a(EUCOMM)Wtsi/Crtc2tm1a(EUCOMM)Wtsi
(B6.B6N-Crtc2tm1a(EUCOMM)Wtsi)
|
increased adipocyte glucose uptake
|
J:229999
|
Crtc3tm1Mmy/Crtc3tm1Mmy
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:167211
|
increased muscle cell glucose uptake
|
J:167211
|
Cry1em1Liga/Cry1em1Liga
(involves: C57BL/6)
|
increased male germ cell apoptosis
|
J:323111
|
oligozoospermia
|
J:323111
|
Cryaatm1.1Ady/Cryaatm1.1Ady
(involves: 129 * C57BL/6)
|
increased lens epithelium apoptosis
|
J:132296
|
increased lens fiber apoptosis
|
J:132296
|
Cryaatm1Wawr/Cryaatm1Wawr
(involves: 129/Sv * 129S4/SvJae)
|
increased lens epithelium apoptosis
|
J:38210
|
Cryaatm1Wawr/Cryaatm1Wawr
(involves: 129S4/SvJae * C57BL/6 * DBA/2)
|
increased lens epithelium apoptosis
|
J:82601
|
Cryabtm1.1Ady/Cryabtm1.1Ady
(involves: 129X1/SvJ * C57BL/6)
|
abnormal reticulophagy
|
J:210399
|
Cryba1tm1.1Dbsa/Cryba1tm1.1Dbsa Tg(BEST1-cre)1Jdun/0
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal lysosome morphology
|
J:215838
|
abnormal lysosome physiology
|
J:215838
|
impaired autophagy
|
J:215838
|
lysosomal protein accumulation
|
J:215531
|
Cryba1tm1a(EUCOMM)Hmgu/Cryba1tm1a(EUCOMM)Hmgu
(involves: C57BL/6J * C57BL/6N)
|
abnormal autophagy
|
J:235696
|
abnormal cell cytoskeleton morphology
|
J:235696
|
abnormal lysosome morphology
|
J:235696
|
abnormal lysosome physiology
|
J:235696
|
increased mitochondrial number
|
J:235696
|
Crybb2tm1Itl/Crybb2tm1Itl
(C57BL/6-Crybb2tm1Itl)
|
abnormal cell cycle
|
J:220082
|
decreased granulosa cell proliferation
|
J:220082
|
decreased mitotic index
|
J:220082
|
increased cellular sensitivity to hydrogen peroxide
|
J:142278
|
increased granulosa cell apoptosis
|
J:220082
|
Csde1tm1Fda/Csde1tm1Fda
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal translation
|
J:252972
|
Csf1op/Csf1op
(C57BL/6J-Csf1op)
|
abnormal osteoblast physiology
|
J:5634
|
Csf1op/Csf1op
(B6C3Fe a/a-Csf1op/J)
|
abnormal osteoclast differentiation
|
J:19549,
J:4732
|
necrospermia
|
J:34371
|
oligozoospermia
|
J:34371
|
Csf1op/Csf1op
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:38039
|
Csf1op/Csf1op
(B6;C3Fe a/a-Csf1op/J)
|
impaired granulosa cell differentiation
|
J:30863
|
impaired macrophage chemotaxis
|
J:147697
|
Csf1op/Csf1op Galctwi/Galctwi
(involves: C3HeB/Fe * C57BL/6J * CE/J)
|
decreased oligodendrocyte progenitor number
|
J:170081
|
impaired macrophage chemotaxis
|
J:170081
|
Csf1tm1.2Sabw/Csf1tm1.2Sabw
(involves: 129S4/SvJaeSor * C57BL/6)
|
impaired osteoblast differentiation
|
J:180199
|
increased osteocyte apoptosis
|
J:180199
|
Csf1rtm1Ers/Csf1r+
(B6.129X1-Csf1rtm1Ers)
|
increased oligodendrocyte progenitor number
|
J:219294
|
Csf1rtm1Ers/Csf1rtm1Ers
(involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:73663
|
oligozoospermia
|
J:73663
|
Csf1rtm1Ers/Csf1rtm1Ers
(FVB.129X1-Csf1rtm1Ers)
|
abnormal macrophage differentiation
|
J:112594
|
Csf2tm1Ard/Csf2tm1Ard
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired macrophage chemotaxis
|
J:86386
|
maternal effect
|
J:53659
|
Csf2raem1Szut/Csf2raem1Szut
(C57BL/6-Csf2raem1Szut)
|
impaired macrophage phagocytosis
|
J:322934
|
Csf2rbtm1Clsc/Csf2rbtm1Clsc Csf2rb2tm1Cgb/Csf2rb2tm1Cgb
(C.129S1-Csf2rb2tm1Cgb Csf2rbtm1Clsc)
|
decreased T cell proliferation
|
J:130939
|
Csf3rtm1Eur/Csf3rtm1Eur
(involves: 129P2/OlaHsd * C57BL/6 * FVB)
|
abnormal neutrophil differentiation
|
J:48503
|
Csf3rtm1Link/Csf3rtm1Link
(involves: 129X1/SvJ)
|
impaired neutrophil chemotaxis
|
J:79825
|
Csf3rtm1Link/Csf3rtm1Link
(B6.129X1-Csf3rtm1Link)
|
impaired neutrophil chemotaxis
|
J:79567
|
Csf3rtm4(Epor)Link/Csf3rtm4(Epor)Link
(involves: 129X1/SvJ * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:79825
|
Csf3rtm4(Epor)Link/Csf3rtm4(Epor)Link
(B6.129X1-Csf3rtm4(Epor)Link)
|
impaired neutrophil chemotaxis
|
J:79567
|
Csgalnact1tm1Nari/Csgalnact1tm1Nari Csgalnact2tm1.1Staka/Csgalnact2tm1.1Staka Tg(Col2a1-cre)1Bhr/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
decreased chondrocyte proliferation
|
J:256718
|
increased chondrocyte apoptosis
|
J:256718
|
Csktm1Sia/Csktm1Sia
(involves: BALB/c * C57BL/6 * CBA)
|
cellular necrosis
|
J:12623
|
cellular phenotype
|
J:12623
|
Csktm2Sia/Csktm2Sia
(involves: BALB/c * C57BL/6 * CBA)
|
cellular necrosis
|
J:12623
|
cellular phenotype
|
J:12623
|
Csltm1(KOMP)Vlcg/Csltm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal tricarboxylic acid cycle
|
J:287403
|
Csn2tm1Psim/Csn2tm1Psim
(involves: 129P2/OlaHsd * MF1)
|
maternal effect
|
J:18947
|
Csnk1a1tm1.1Ybn/Csnk1a1tm1.1Ybn Tg(KRT14-cre/ERT)20Efu/0
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:253611
|
increased apoptosis
|
J:253611
|
Csnk1a1tm1.1Ybn/Csnk1a1tm1.1Ybn Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129 * C57BL/6 * CD-1 * DBA/2)
|
increased apoptosis
|
J:204886
|
increased fibroblast apoptosis
|
J:204886
|
Csnk1a1tm1.1Ybn/Csnk1a1tm1.1Ybn Tg(Vil1-cre/ERT2)23Syr/0 Trp53tm1Brn/Trp53tm1Brn
(involves: 129 * C57BL/6 * CD-1 * DBA/2)
|
abnormal enterocyte proliferation
|
J:204886
|
increased apoptosis
|
J:204886
|
Csnk1a1tm1.1Ybn/Csnk1a1tm1.1Ybn Tg(Vil1-cre/ERT2)23Syr/0 Trp53tm3.1Tyj/Trp53tm3.1Tyj
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal enterocyte proliferation
|
J:291671
|
Csnk1a1tm1.1Ybn/Csnk1a1tm1.1Ybn Trp53tm1Brn/Trp53tm1Brn Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal enterocyte proliferation
|
J:291671
|
Csnk1a1tm1.1Ybn/Csnk1a1tm1.1Ybn Trp53tm2.1Tyj/Trp53tm2.1Tyj Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129S1/Sv * 129X1/SvJ * 129S4/SvJae * C57BL/6 * DBA/2)
|
abnormal enterocyte proliferation
|
J:291671
|
Csnk1g2em1Xidw/Csnk1g2em1Xidw
(Not Specified)
|
increased sensitivity to induced cell death
|
J:298682
|
Csnk2a2tm1Dcs/Csnk2a2tm1Dcs
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal acrosome morphology
|
J:85522
|
abnormal sperm head morphology
|
J:57312
|
abnormal sperm motility
|
J:57312
|
abnormal sperm nucleus morphology
|
J:57312
|
abnormal spermatid morphology
|
J:57312,
J:85522
|
abnormal spermatocyte morphology
|
J:85522
|
abnormal spermatogonia morphology
|
J:85522
|
coiled sperm flagellum
|
J:85522
|
detached acrosome
|
J:57312,
J:85522
|
globozoospermia
|
J:57312
|
increased male germ cell apoptosis
|
J:57312
|
kinked sperm flagellum
|
J:57312,
J:85522
|
oligozoospermia
|
J:57312,
J:85522
|
teratozoospermia
|
J:57312
|
Csnk2btm1.1Bb/Csnk2btm1.1Bb Tg(Gdf9-icre)5092Coo/0
(involves: 129S2/SvPasCrl * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:305036
|
decreased oocyte number
|
J:305036
|
increased granulosa cell apoptosis
|
J:305036
|
Csnk2btm1.1Bb/Csnk2btm1.2Bb Tg(Stra8-icre)1Reb/0
(involves: 129S2/SvPasCrl * C57BL/6 * FVB/NJ)
|
abnormal spermatocyte morphology
|
J:289955
|
azoospermia
|
J:289955
|
decreased elongated spermatid number
|
J:289955
|
decreased male germ cell number
|
J:289955
|
decreased round spermatid number
|
J:289955
|
decreased spermatid number
|
J:289955
|
increased male germ cell apoptosis
|
J:289955
|
increased testis apoptosis
|
J:289955
|
Cspg4tm1Wbst/Cspg4tm1Wbst
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell migration
|
J:54319
|
decreased cell proliferation
|
J:54319
|
Csrp3tm1Crni/Csrp3tm1Crni
(Not Specified)
|
abnormal actin cytoskeleton morphology
|
J:38213
|
cardiac interstitial fibrosis
|
J:38213
|
Csrp3tm1Crni/Csrp3tm1Crni Tg(Myh6-ADRBK1)27Wjk/0
(involves: C57BL/6 * SJL)
|
cardiac interstitial fibrosis
|
J:48062
|
Cst3tm1(CST3*L68Q)Cnw/Cst3+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal male germ cell morphology
|
J:210672
|
asthenozoospermia
|
J:210672
|
Cst6ichq/Cst6+
(involves: BALB/cJ)
|
abnormal mitochondrial morphology
|
J:41426
|
increased keratinocyte proliferation
|
J:41426
|
Cst7tm1.2Arte/Cst7tm1.2Arte
(involves: C57BL/6)
|
increased apoptosis
|
J:258944
|
Cst8tm1Itl/Cst8tm1Itl
(involves: 129S6/SvEvTac * C57BL/6)
|
asthenozoospermia
|
J:168157
|
decreased sperm progressive motility
|
J:168157
|
oligozoospermia
|
J:168157
|
Csta1em1Gpt/Csta1em1Gpt
(C57BL/6JGpt-Csta1em1Gpt)
|
decreased keratinocyte proliferation
|
J:340112
|
Cstbtm1Rm/Cstbtm1Rm
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal apoptosis
|
J:50587
|
Cstf2ttm1Ccma/Cstf2ttm1Ccma
(involves: 129S/SvEv * C57BL/6)
|
abnormal spermatid morphology
|
J:130584
|
asthenozoospermia
|
J:130584
|
globozoospermia
|
J:130584
|
oligozoospermia
|
J:130584
|
teratozoospermia
|
J:130584
|
Ct55em2Xdzg/Y
(C57BL/6-Ct55em2Xdzg)
|
abnormal acrosome assembly
|
J:337211
|
abnormal acrosome morphology
|
J:337211
|
abnormal Golgi apparatus morphology
|
J:337211
|
abnormal round spermatid morphology
|
J:337211
|
abnormal sperm fibrous sheath morphology
|
J:337211
|
abnormal sperm mitochondrial sheath morphology
|
J:337211
|
asthenozoospermia
|
J:337211
|
decreased sperm progressive motility
|
J:337211
|
impaired autophagy
|
J:337211
|
oligozoospermia
|
J:337211
|
Ctbstm1Tbec/Ctbstm1Tbec
(involves: 129S2/SvPas * C57BL/6N)
|
abnormal cell physiology
|
J:185162
|
Ctc1tm1.1Schg/Ctc1tm1.1Schg
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal DNA repair
|
J:184809
|
abnormal telomere length
|
J:184809
|
chromosomal instability
|
J:184809
|
decreased cell proliferation
|
J:184809
|
decreased fibroblast proliferation
|
J:184809
|
decreased splenocyte proliferation
|
J:184809
|
early cellular replicative senescence
|
J:184809
|
Ctcftm1.1Gfili/Ctcftm1.1Gfili
(involves: 129S4/SvJaeSor * C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:211097
|
Ctcfltm1Vloc/Ctcfltm1Vloc
(involves: 129S1/Sv * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:162590
|
abnormal male meiosis
|
J:162590
|
Ctdnep1tm1Ryn/Ctdnep1+ Wnt3tm1Brd/Wnt3+
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6)
|
decreased primordial germ cell number
|
J:199855
|
Ctdnep1tm1Ryn/Ctdnep1tm1Ryn
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal primordial germ cell morphology
|
J:199855
|
decreased primordial germ cell number
|
J:199855
|
Ctdnep1tm2Ryn/Ctdnep1tm2Ryn
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal primordial germ cell morphology
|
J:199855
|
decreased primordial germ cell number
|
J:199855
|
Ctdnep1tm3Ryn/Ctdnep1tm3Ryn Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ Six2tm1(tTA,tetO-EGFP/cre)Amc/Six2+
(involves: 129X1/SvJ * C57BL/6 * C57BL/6J)
|
decreased kidney apoptosis
|
J:205755
|
Ctdp1em1.1Ntw/Ctdp1em1.1Ntw
(involves: C57BL/6 * FVB)
|
increased apoptosis
|
J:320982
|
Ctdp1em1Ntw/Ctdp1em1Ntw
(involves: C57BL/6 * FVB)
|
decreased fibroblast proliferation
|
J:320982
|
increased fibroblast apoptosis
|
J:320982
|
Ctf1tm1Msd/Ctf1tm1Msd
(B6.Cg-Ctf1tm1Msd)
|
abnormal aerobic respiration
|
J:176727
|
decreased fat cell mitochondrial DNA content
|
J:176727
|
Cthtm1Iish/Cthtm1Iish
(B6.129-Cthtm1Iish/Iish)
|
increased cellular sensitivity to oxidative stress
|
J:166184
|
increased sensitivity to induced cell death
|
J:166184
|
Cthrc1tm1Haak/Cthrc1tm1Haak
(B6.129S-Cthrc1tm1Haak)
|
abnormal osteoblast physiology
|
J:143940
|
decreased osteoblast proliferation
|
J:143940
|
Ctla4tm1All/Ctla4tm1All Rag1tm1Mom/Rag1tm1Mom Tg(TcrAND)53Hed/0
(involves: 129S/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
increased T cell proliferation
|
J:119845
|
Ctla4tm1Shr/Ctla4tm1Shr
(either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6))
|
increased T cell proliferation
|
J:30393
|
Ctla4tm1Shr/Ctla4tm1Shr Tg(DO11.10)10Dlo/0
(involves: 129S4/SvJae * BALB/c * C3H * C57BL/6)
|
increased T cell proliferation
|
J:57090
|
Ctnna1tm1Efu/Ctnna1tm1Efu Tg(KRT14-cre)1Efu/?
(involves: 129X1/SvJ)
|
abnormal cell adhesion
|
J:67797
|
increased keratinocyte proliferation
|
J:67797
|
Ctnna1tm1Efu/Ctnna1tm1Efu Tg(Nes-cre)1Kln/?
(involves: 129X1/SvJ * C57BL/6 * SJL)
|
abnormal mitosis
|
J:106707
|
abnormal neuron differentiation
|
J:106707
|
Ctnna1tm1Efu/Ctnna1tm1Efu Tg(Wap-cre)11738Mam/?
(involves: 129X1/SvJ * C57BL/6 * SJL)
|
maternal effect
|
J:87469
|
Ctnnal1Gt(RRJ603)Byg/Ctnnal1Gt(RRJ603)Byg
(involves: 129P2/OlaHsd)
|
abnormal actin cytoskeleton morphology
|
J:308883
|
impaired basement membrane formation
|
J:308883
|
Ctnnb1tm1(Nfkbia)Rsu/Ctnnb1+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:71744
|
increased hair follicle apoptosis
|
J:71744
|
increased hepatocyte apoptosis
|
J:71744
|
Ctnnb1tm1Max/Ctnnb1tm2Kem Tg(Msx2-cre)5Rem/0
(involves: 129S1/Sv * 129X1/SvJ)
|
increased ectoderm apoptosis
|
J:81795
|
Ctnnb1tm1Max/Ctnnb1tm2Kem Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
arrested osteoblast differentiation
|
J:114494
|
Ctnnb1tm1Mmt/Ctnnb1+
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ)
|
abnormal small intestinal crypt cell proliferation
|
J:169830
|
Ctnnb1tm1Mmt/Ctnnb1+ Ctsktm1(cre)Ska/Ctsk+
(involves: 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal osteoclast differentiation
|
J:178340
|
Ctnnb1tm1Mmt/Ctnnb1+ Krastm4Tyj/Kras+ Tg(CYP19A1-cre)1Jri/0
(involves: 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
impaired granulosa cell differentiation
|
J:186144
|
Ctnnb1tm1Mmt/Ctnnb1+ Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129X1/SvJ)
|
abnormal osteoclast differentiation
|
J:178340
|
Ctnnb1tm1Mmt/Ctnnb1+ Nanos3tm2(cre)Ysa/Nanos3+
(involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
decreased spermatogonia number
|
J:257319
|
Ctnnb1tm1Mmt/Ctnnb1+ Ppargtm1.1(tTA)Jmgr/Pparg+ Tg(tetO-cre)1Jaw/0
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6)
|
abnormal osteoclast differentiation
|
J:178340
|
Ctnnb1tm1Mmt/Ctnnb1+ Ptentm1Hwu/Ptentm1Hwu Tg(CYP19A1-cre)1Jri/0
(involves: 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
decreased granulosa cell apoptosis
|
J:186144
|
impaired granulosa cell differentiation
|
J:186144
|
increased granulosa cell proliferation
|
J:186144
|
Ctnnb1tm1Mmt/Ctnnb1+ Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
(involves: 129X1/SvJ * CD-1)
|
abnormal osteoblast differentiation
|
J:114494
|
abnormal osteoclast differentiation
|
J:114494
|
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt Nanos3tm2(cre)Ysa/Nanos3+
(involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
decreased spermatogonia number
|
J:257319
|
Ctnnb1tm1Mmt/Ctnnb1tm1Mmt Tg(Cryaa-cre)10Mlr/0
(involves: 129X1/SvJ * FVB/N)
|
increased lens epithelium apoptosis
|
J:152850
|
Ctnnb1tm1Yy/Ctnnb1tm1.1Yy Ptch1tm1Yy/Ptch1tm1.1Yy Tg(Col2a1-cre)1Bhr/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
arrested osteoblast differentiation
|
J:112462
|
Ctnnb1tm1Yy/Ctnnb1tm1.1Yy Tg(Col2a1-cre)1Bhr/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased chondrocyte apoptosis
|
J:112462
|
Ctnnb1tm2(Nfkbia)Rsu/Ctnnb1+ Tg(CMV-cre)1Cgn/0
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:71744
|
increased hepatocyte apoptosis
|
J:71744
|
Ctnnb1tm2Kem/Ctnnb1+ Nanos3tm2(cre)Ysa/Nanos3+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj)
|
decreased spermatogonia number
|
J:257319
|
Ctnnb1tm2Kem/Ctnnb1tm2.1Kem Corintm2(cre)Bamo/Corin+ Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
increased hair follicle apoptosis
|
J:160311
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129 * C57BL/6 * CBA/J)
|
premature neuronal precursor differentiation
|
J:178971
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Juptm1Ruiz/Juptm1Ruiz Olig2tm1(cre)Tmj/Olig2+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
abnormal neuronal migration
|
J:178688
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Nanos3tm2(cre)Ysa/Nanos3+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj)
|
decreased spermatogonia number
|
J:257319
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Ppargtm1.1(tTA)Jmgr/Pparg+ Tg(tetO-cre)1Jaw/0 Tg(tetO-HIST1H2BJ/GFP)47Efu/0
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
|
abnormal osteoclast differentiation
|
J:178340
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Dct-lacZ)A12Jkn/0 Tg(Tyr-cre)1Lru/0
(B6.Cg-Ctnnb1tm2Kem Tg(Tyr-cre)1Lru Tg(Dct-lacZ)A12Jkn)
|
decreased melanoblast proliferation
|
J:176245
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Hoxb7-cre)5526Cmb/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
decreased kidney cell proliferation
|
J:136068
|
increased metanephric mesenchyme apoptosis
|
J:136068
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(KRT5-rtTA)#Glk/0 Tg(tetO-cre)1Jaw/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
increased hair follicle apoptosis
|
J:204142
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(KRT14-cre)#Smr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)
|
decreased cell proliferation
|
J:242196
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(KRT14-rtTA)F42Efu/0 Tg(tetO-EDN1,-lacZ)9Mhus/0 Tg(Tyr-cre/ERT2)13Bos/0
(involves: C57BL/6J * FVB)
|
abnormal melanocyte differentiation
|
J:231435
|
abnormal melanocyte proliferation
|
J:231435
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA)
|
abnormal vascular regression
|
J:144980
|
Ctnnb1tm2Kem/Ctnnb1tm2Kem Twist2tm1(cre)Dor/Twist2+
(involves: 129S1/Sv * 129X1/SvJ)
|
arrested osteoblast differentiation
|
J:178499
|
Ctnnb1tm2Kem/Ctnnb1tm3Kba H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129 * C57BL/6 * CBA/J)
|
abnormal neuron differentiation
|
J:178971
|
Ctnnbip1tm1Taki/Ctnnbip1tm1Taki
(involves: C57BL/6 * CBA)
|
abnormal apoptosis
|
J:90666
|
increased metanephric mesenchyme apoptosis
|
J:125187
|
Ctnnd1tm1Abre/Ctnnd1tm1Abre
(involves: 129S6/SvEvTac)
|
abnormal mitosis
|
J:143096
|
abnormal mitotic spindle morphology
|
J:143096
|
binucleate
|
J:143096
|
decreased cell proliferation
|
J:143096
|
Ctnnd1tm1Abre/Ctnnd1tm1Abre Tg(KRT14-cre)1Efu/?
(involves: 129S6/SvEvTac)
|
binucleate
|
J:143096
|
Ctnnd1tm1Abre/Ctnnd1tm1Abre Tg(MMTV-cre)FMam/0
(involves: 129S6/SvEvTac * Black Swiss * C57BL/6 * FVB/N)
|
increased submandibular gland apoptosis
|
J:105283
|
Ctnnd1tm1Lfr/Ctnnd1tm1Lfr Tg(Pax3-cre)1Joe/0
(involves: 129X1/SvJ * C57BL/6 * SJL)
|
abnormal cell adhesion
|
J:171425
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:171425
|
increased kidney apoptosis
|
J:171425
|
increased kidney cell proliferation
|
J:171425
|
Ctnstm1Antc/Ctnstm1Antc
(involves: 129/Sv * C57BL/6)
|
dilated mitochondrion
|
J:79610
|
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi Commd10Tg(Vav1-icre)A2Kio/0
(B6.Cg-Ctps1tm1c(KOMP)Wtsi Commd10Tg(Vav1-icre)A2Kio)
|
decreased T cell proliferation
|
J:348981
|
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi Ctps2tm1c(EUCOMM)Hmgu/Ctps2+ Tg(Cd4-cre)1Cwi/0
(involves: 129S/Sv * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:348981
|
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi Ctps2tm1c(EUCOMM)Hmgu/Ctps2tm1c(EUCOMM)Hmgu Tg(Cd4-cre)1Cwi/0
(involves: 129S/Sv * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:348981
|
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(B6.Cg-Ctps1tm1c(KOMP)Wtsi Gt(ROSA)26Sortm1(cre/ERT2)Tyj)
|
decreased T cell proliferation
|
J:348981
|
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi Tg(Cd4-cre)1Cwi/0
(involves: 129S/Sv * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:348981
|
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi Tg(Cd4-cre)1Cwi/0 Foxp3sf/Y Rag1tm1Mom/Rag1+
(mixed)
|
decreased T cell proliferation
|
J:348981
|
Ctps1tm1c(KOMP)Wtsi/Ctps1tm1c(KOMP)Wtsi Tg(Cd8a-cre)1Itan/0
(B6(129S4)-Ctps1tm1c(KOMP)Wtsi Tg(Cd8a-cre)1Itan)
|
decreased T cell proliferation
|
J:348981
|
Ctsatm1Adz/Ctsatm1Adz
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/NJ))
|
abnormal lysosome morphology
|
J:29674
|
Ctsbtm1Jde/Ctsbtm1Jde
(involves: 129P2/OlaHsd)
|
decreased apoptosis
|
J:96164
|
Ctsbtm1Jde/Ctsbtm1Jde Ctsltm1Cptr/Ctsltm1Cptr
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal neuron apoptosis
|
J:77103
|
Ctsbtm1Jde/Ctsbtm1Jde Ctsztm1Thre/Ctsztm1Thre Tg(MMTV-PyVT)634Mul/0
(FVB.129P2-Ctsztm1Thre Ctsbtm1Jde Tg(MMTV-PyVT)634Mul)
|
decreased apoptosis
|
J:157541
|
Ctsctm1Ley/Ctsctm1Ley
(B6.129X1-Ctsctm1Ley)
|
abnormal leukocyte migration
|
J:131520
|
Ctsdtm1Cptr/Ctsdtm1Cptr
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd))
|
cellular phenotype
|
J:28201
|
increased forebrain apoptosis
|
J:71688
|
lysosomal protein accumulation
|
J:64892
|
Ctsktm1(cre)Ska/Ctsk+ Plekhm1tm1.1Hzhao/Plekhm1tm1.1Hzhao
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal lysosome morphology
|
J:236517
|
decreased lysosomal enzyme secretion
|
J:236517
|
Ctsktm1.1Rbar/Ctsktm1.1Rbar Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal osteoblast differentiation
|
J:194492
|
abnormal osteoblast physiology
|
J:194492
|
abnormal osteoclast differentiation
|
J:194492
|
Ctsktm1Mbs/Ctsktm1Mbs
(B6.129-Ctsktm1Mbs)
|
abnormal osteoblast physiology
|
J:128098
|
Ctsltm1.2Thre/Ctsltm1.2Thre
(involves: C57BL/6 * C57BL/6N)
|
increased keratinocyte proliferation
|
J:216506
|
Ctsltm1Cptr/Ctsltm1Cptr
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased keratinocyte proliferation
|
J:70118
|
Ctsltm1Cptr/Ctsltm1Cptr
(involves: 129P2/OlaHsd)
|
abnormal lysosome morphology
|
J:216506
|
cardiac interstitial fibrosis
|
J:76333
|
increased keratinocyte proliferation
|
J:216506
|
Ctsstm1Hap/Ctsstm1Hap Ldlrtm1Her/Ldlrtm1Her
(B6.129S-Ctsstm1Hap Ldlrtm1Her)
|
abnormal leukocyte migration
|
J:82520
|
Ctsstm1Hap/Ctsstm1Hap Tg(Scgb1a1-rtTA,tetO-Ifng)14Eli/0
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
increased apoptosis
|
J:100854
|
Ctsztm1Thre/Ctsztm1Thre Tg(MMTV-PyVT)634Mul/0
(FVB.129P2-Ctsztm1Thre Tg(MMTV-PyVT)634Mul)
|
decreased apoptosis
|
J:157541
|
CttnGt(RRS284)Byg/Cttn+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell morphology
|
J:158029
|
CttnGt(RRS284)Byg/CttnGt(RRS284)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal secondary polar body morphology
|
J:158029
|
Cttntm1.1Okab/Cttntm1.1Okab
(involves: 129S4/SvJae * C57BL/6 * SJL)
|
cellular phenotype
|
J:155986
|
Cttntm1.2Dvst/Cttntm1.2Dvst
(either: B6.Cg-Cttntm1.2Dvst or (involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA/2 * SJL))
|
abnormal cellular extravasation
|
J:177602
|
abnormal leukocyte adhesion
|
J:177602
|
abnormal leukocyte migration
|
J:177602
|
Cttntm1.2Okab/Cttntm1.2Okab
(involves: 129S4/SvJae * BALB/cJ * C57BL/6 * SJL)
|
cellular phenotype
|
J:155986
|
Cul1tm1Rsjo/Cul1tm1Rsjo
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:57767
|
Cul1tmTye/Cul1tmTye
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:58150
|
increased apoptosis
|
J:58150
|
Cul3em1Limi/Cul3+
(C57BL/6N-Cul3em1Limi)
|
abnormal actin cytoskeleton morphology
|
J:332937
|
Cul3tm1Jdsr/Cul3tm1Jdsr
(involves: 129S4/SvJaeSor)
|
abnormal cell cycle
|
J:122228
|
increased fibroblast apoptosis
|
J:122228
|
Cul3tm1Jro/Cul3+
(involves: 129S4/SvJaeSor)
|
abnormal cell cycle
|
J:122228
|
Cul4a/Pcid2tm2Ktc/Cul4a/Pcid2tm2Ktc Tg(Mx1-cre)1Cgn/0
(involves: 129S/SvEv * C57BL/6 * CBA * FVB/N)
|
increased enterocyte apoptosis
|
J:138468
|
Cul4a/Pcid2tm2Ktc/Cul4a/Pcid2tm2Ktc Tg(Mx1-cre)1Cgn/0
(involves: 129S/SvEv * C57BL/6 * CBA * FVB/N)
|
increased enterocyte apoptosis
|
J:138468
|
Cul4atm1.1Pra/Cul4atm1.1Pra
(involves: C57BL/6NTac)
|
abnormal cell cycle checkpoint function
|
J:172043
|
abnormal centrosome morphology
|
J:172043
|
abnormal DNA replication
|
J:172043
|
chromosomal instability
|
J:172043
|
decreased fibroblast proliferation
|
J:172043
|
increased cellular sensitivity to ultraviolet irradiation
|
J:172043
|
Cul4atm1.1Pra/Cul4atm1.1Pra Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * C57BL/6NTac * DBA)
|
decreased hepatocyte proliferation
|
J:172043
|
Cul4atm1.2Pra/Cul4atm1.2Pra
(Not Specified)
|
abnormal double-strand DNA break repair
|
J:171470
|
abnormal male meiosis
|
J:171470
|
abnormal sperm flagellum morphology
|
J:171470
|
abnormal sperm head morphology
|
J:171470
|
abnormal spermatid morphology
|
J:171470
|
abnormal spermatocyte morphology
|
J:171470
|
asthenozoospermia
|
J:171470
|
azoospermia
|
J:171470
|
increased male germ cell apoptosis
|
J:171470
|
multinucleated giant male germ cells
|
J:171470
|
oligozoospermia
|
J:171470
|
Cul4atm1.2Pz/Cul4atm1.2Pz
(B6.Cg-Cul4atm1.2Pz)
|
abnormal cell cycle checkpoint function
|
J:150427
|
abnormal DNA repair
|
J:150427
|
Cul4btm1.1Pz/Y Tg(CAG-cre)13Miya/0
(involves: 129 * C57BL/6 * C57BL/6J)
|
decreased cell proliferation
|
J:199210
|
increased embryonic tissue cell apoptosis
|
J:199210
|
Cul4btm1.1Yxg/Y
(involves: 129X1/SvJ * FVB/N)
|
decreased cell proliferation
|
J:199139
|
increased embryonic tissue cell apoptosis
|
J:199139
|
Cul4btm1.1Yxg/Cul4b+
(involves: 129X1/SvJ * FVB/N)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:199139
|
Cul7tm1Zqp/Cul7tm1Zqp
(involves: 129S/SvEv * C57BL/6J)
|
early cellular replicative senescence
|
J:137062
|
Cul9tm1.2Yxi/Cul9tm1.2Yxi
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
cellular phenotype
|
J:170976
|
decreased cellular sensitivity to gamma-irradiation
|
J:170976
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:170976
|
Cux2Gt(OST440231)Lex/Cux2Gt(OST440231)Lex
(involves: 129S5/SvEvBrd)
|
abnormal cell cycle
|
J:131816
|
decreased cell proliferation
|
J:131816
|
Cux2tm1.1Nieto/Cux2tm1.1Nieto
(involves: 129S4/SvJae * C57BL/6 * FVB/N * Swiss Webster)
|
abnormal neuronal precursor proliferation
|
J:156578
|
Cuzd1tm1Bag/Cuzd1tm1Bag
(involves: 129 * C57BL/6)
|
decreased mammary gland epithelial cell proliferation
|
J:242064
|
maternal effect
|
J:242064
|
Cwh43em1Mdj/Cwh43em1Mdj
(C57BL/6-Cwh43em1Mdj)
|
decreased brain ependyma motile cilium number
|
J:310176
|
Cwh43em1Mdj/Cwh43em2Mdj
(C57BL/6-Cwh43em1Mdj/Cwh43em2Mdj)
|
decreased brain ependyma motile cilium number
|
J:310176
|
Cx3cl1tm1Lira/Cx3cl1tm1Lira
(Not Specified)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:110266
|
Cx3cl1tm1Sgs/Cx3cl1tm1Sgs Ldlrtm1Her/Ldlrtm1Her
(involves: B6.129S4-Cx3cl1tm1Sgs * B6.129S7-Ldlrtm1Her/J)
|
impaired macrophage chemotaxis
|
J:95279
|
Cx3cr1tm1Ifc/Cx3cr1tm1Ifc
(involves: 129S4/SvJae * C57BL/6)
|
impaired macrophage chemotaxis
|
J:82033
|
Cx3cr1tm1Litt/Cx3cr1tm1Litt
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired macrophage chemotaxis
|
J:162714
|
Cx3cr1tm1Litt/Cx3cr1tm1Litt
(B6.129P2-Cx3cr1tm1Litt)
|
abnormal photoreceptor connecting cilium morphology
|
J:265696
|
decreased vascular smooth muscle cell proliferation
|
J:124722
|
increased neuron apoptosis
|
J:110266
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:110266
|
Cx3cr1tm2.1(cre/ERT2)Litt/Cx3cr1+ Vps35Gt(RRK261)Byg/Vps35Gt(RRK261)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased neuron apoptosis
|
J:292365
|
Cxadrtm1.1Mds/Cxadrtm1.1Mds
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J)
|
abnormal fetal cardiomyocyte proliferation
|
J:121400
|
Cxadrtm1Dvst/Cxadrtm1Dvst
(involves: 129X1/SvJ * C57BL/6)
|
abnormal mitochondrial morphology
|
J:100174
|
Cxadrtm1Rwf/Cxadrtm1Rwf
(involves: 129S6/SvEvTac * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:99585
|
Cxcl10tm1Adl/Cxcl10tm1Adl
(involves: 129S4/SvJae * 129X1/SvJ)
|
decreased splenocyte proliferation
|
J:75584
|
Cxcl12tm1Tng/Cxcl12tm1Tng
(B6.Cg-Cxcl12tm1Tng)
|
abnormal primordial germ cell migration
|
J:83291
|
Cxcl12tm3.1(HBEGF/EGFP)Tng/Cxcl12+
(B6.Cg-Cxcl12tm3.1(HBEGF/EGFP)Tng)
|
increased B cell apoptosis
|
J:164657
|
Cxcl13tm1Cys/Cxcl13tm1Cys
(B6.129X1-Cxcl13tm1Cys)
|
impaired B cell migration
|
J:118931
|
Cxcl13tm1Mmi/Cxcl13tm1Mmi
(involves: C57BL/6)
|
abnormal leukocyte adhesion
|
J:84804
|
abnormal leukocyte migration
|
J:84804
|
Cxcr2tm1Mwm/Cxcr2tm1Mwm
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal granulocyte differentiation
|
J:19570
|
impaired neutrophil chemotaxis
|
J:19570
|
Cxcr2tm1Mwm/Cxcr2tm1Mwm
(C.129S2(B6)-Cxcr2tm1Mwm/J)
|
decreased oligodendrocyte progenitor number
|
J:78470
|
impaired neutrophil chemotaxis
|
J:65905,
J:72824
|
Cxcr3tm1Wwh/Y
(B6.Cg-Cxcr3tm1Wwh)
|
abnormal cellular extravasation
|
J:107646
|
impaired macrophage chemotaxis
|
J:107646
|
Cxcr3tm1Wwh/Cxcr3tm1Wwh
(B6.Cg-Cxcr3tm1Wwh)
|
abnormal cellular extravasation
|
J:96905,
J:107646
|
impaired macrophage chemotaxis
|
J:107646
|
Cxcr4tm1.1Bala/Cxcr4+
(B6.129S2-Cxcr4tm1.1Bala)
|
abnormal cell chemotaxis
|
J:186735
|
decreased B cell apoptosis
|
J:186735
|
Cxcr4tm1Qma/Cxcr4tm1Qma
(B6.129X-Cxcr4tm1Qma/J)
|
abnormal muscle precursor cell migration
|
J:100909
|
Cxcr4tm1Qma/Cxcr4tm1Qma Gab1tm1Wbm/Gab1tm1Wbm
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6)
|
abnormal muscle precursor cell migration
|
J:100909
|
Cxcr4tm1Tng/Cxcr4tm1Tng
(B6.Cg-Cxcr4tm1Tng)
|
abnormal primordial germ cell migration
|
J:83291
|
Cxcr4tm1Yiw/Cxcr4tm1Yiw Tg(Lck-cre)1Jtak/0
(involves: 129P2/OlaHsd)
|
abnormal leukocyte migration
|
J:164872
|
Cxcr4tm1Yzo/Cxcr4tm1Yzo
(Not Specified)
|
abnormal primordial germ cell migration
|
J:84597
|
decreased primordial germ cell number
|
J:84597
|
Cxcr4tm2Yzo/Cxcr4tm2Yzo Tg(Myh6-cre)2182Mds/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
cardiac interstitial fibrosis
|
J:289614
|
Cxcr5tm1.1Namt/Cxcr5tm1.1Namt Tg(Itgax-cre)1-1Reiz/0
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal dendritic cell chemotaxis
|
J:241561
|
Cxcr5tm1Lipp/Cxcr5tm1Lipp
(involves: 129S2/SvPas * CD-1)
|
abnormal leukocyte migration
|
J:37126
|
Cxxc1tm2.1Skk/Cxxc1tm2.1Skk Tg(Stra8-icre)1Reb/0
(involves: FVB/NJ)
|
abnormal acrosome morphology
|
J:329283
|
abnormal chromosomal synapsis
|
J:329283
|
abnormal epigenetic regulation of gene expression
|
J:329283
|
arrest of male meiosis
|
J:329283
|
azoospermia
|
J:329283
|
decreased male germ cell number
|
J:329283
|
increased male germ cell apoptosis
|
J:329283
|
increased spermatogonia number
|
J:329283
|
Cxxc5tm1Kych/Cxxc5tm1Kych
(involves: 129S1/Sv)
|
enhanced osteoblast differentiation
|
J:226604
|
Cyb5r2tm1a(EUCOMM)Hmgu/Cyb5r2tm1a(EUCOMM)Hmgu
(FVB.B6N-Cyb5r2tm1a(EUCOMM)Hmgu)
|
cellular phenotype
|
J:211614
|
Cybanmf333/Cybanmf333
(involves: A * C57BL/6)
|
abnormal intestinal goblet cell physiology
|
J:206181
|
Cybatm1Dgh/Cybatm1Dgh
(B6.Cg-Cybatm1Dgh)
|
abnormal redox activity
|
J:231269
|
Cybbtm1.1Abk/Cybbtm1.1Abk Lyz2tm1(cre)Ifo/?
(B6.Cg-Lyz2tm1(cre)Ifo Cybbtm1.1Abk)
|
abnormal macrophage chemotaxis
|
J:245699
|
Cybbtm1Din/?
(B6.129S-Cybbtm1Din/J)
|
abnormal redox activity
|
J:306955
|
decreased cell proliferation
|
J:306955
|
increased apoptosis
|
J:306955
|
Cybbtm1Din/Cybbtm1Din Nrrostm1Lex/Nrrostm1Lex
(B6.129S-Nrrostm1Lex Cybbtm1Din)
|
cellular phenotype
|
J:209569
|
Cycstm1Arte/Cycstm1Arte
(Not Specified)
|
cellular phenotype
|
J:210495
|
Cycstm1Mak/Cycstm1Mak
(involves: C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:98949
|
Cycstm1Wlm/Cycstm1Wlm
(involves: 129X1/SvJ * C57BL/6)
|
abnormal apoptosis
|
J:62276
|
abnormal cellular respiration
|
J:62276
|
Cycttm1Jlm/Cycttm1Jlm
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal oxidative phosphorylation
|
J:77908
|
abnormal sperm motility
|
J:77908
|
oligozoospermia
|
J:77908
|
Cygbtm1Ppam/Cygbtm1Ppam Tg(Myog-cre)1Eno/0
(involves: 129 * C57BL/6)
|
abnormal myoblast differentiation
|
J:206378
|
decreased cell proliferation
|
J:206378
|
increased apoptosis
|
J:206378
|
oxidative stress
|
J:206378
|
Cylc1em1Chnsr/Y
(involves: C57BL/6JGpt)
|
abnormal sperm head morphology
|
J:347872
|
detached acrosome
|
J:347872
|
Cylc1em2Chnsr/Y
(involves: C57BL/6JGpt)
|
abnormal sperm head morphology
|
J:347872
|
detached acrosome
|
J:347872
|
Cyldtm1.1Gmos/Cyldtm1.1Gmos
(involves: BALB/cJ)
|
impaired fibroblast cell migration
|
J:162840
|
Cyldtm1Ref/Cyldtm1Ref
(B6.129-Cyldtm1Ref)
|
abnormal keratinocyte proliferation
|
J:108769
|
increased cell proliferation
|
J:108769
|
increased keratinocyte proliferation
|
J:108769
|
Cyp2b10tm1a(KOMP)Wtsi/Cyp2b10tm1a(KOMP)Wtsi
(C57BL/6N-Cyp2b10tm1a(KOMP)Wtsi)
|
abnormal lipid oxidation
|
J:339440
|
Cyp2c23Gt(OST85045)Lex/Cyp2c23Gt(OST85045)Lex
(129-Cyp2c23Gt(OST85045)Lex)
|
decreased lung endothelial cell proliferation
|
J:207597
|
Cyp2g1tm1(rtTA)Lane/Cyp2g1+ Tg(SFTPC-rtTA,tetO-Tnf)320-1Gwho/0
(involves: 129 * C57BL/6 * SJL)
|
decreased cell proliferation
|
J:157842
|
Cyp4f18tm1.1Pchr/Cyp4f18tm1.1Pchr
(B6.Cg-Cyp4f18tm1.1Pchr)
|
abnormal fatty acid oxidation
|
J:212489
|
Cyp4v3em1Xsu/Cyp4v3em1Xsu
(C57BL/6J-Cyp4v3em1Xsu)
|
oxidative stress
|
J:321817
|
Cyp11a1tm1.1Bcc/Cyp11a1tm1.1Bcc
(B6.129(FVB)-Cyp11a1tm1.1Bcc)
|
abnormal mitochondrial morphology
|
J:191801
|
Cyp11a1tm2Bcc/Cyp11a1tm2Bcc
(Not Specified)
|
abnormal mitochondrial morphology
|
J:133007
|
decreased T cell apoptosis
|
J:133007
|
Cyp11b2tm2Hsk/Cyp11b2tm2Hsk
(involves: 129S6/SvEvTac)
|
oxidative stress
|
J:147672
|
Cyp17a1tm1Vpap/Cyp17a1+
(chimera involves: 129X1/SvJ * C57BL/6)
|
abnormal sperm flagellum morphology
|
J:100434
|
asthenozoospermia
|
J:100434
|
Cyp19a1tm1Esi/Cyp19a1tm1Esi
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal acrosome assembly
|
J:56358
|
abnormal male germ cell morphology
|
J:56358
|
decreased elongated spermatid number
|
J:56358
|
decreased male germ cell number
|
J:56358
|
decreased round spermatid number
|
J:56358
|
decreased spermatid number
|
J:56358
|
increased granulosa cell apoptosis
|
J:63458
|
increased male germ cell apoptosis
|
J:56358
|
multinucleated giant male germ cells
|
J:56358
|
Cyp19a1tm1Esi/Cyp19a1tm1Esi
(involves: 129S6/SvEvTac)
|
asthenozoospermia
|
J:83254
|
oligozoospermia
|
J:83254
|
Cyp19a1tm1Toda/Cyp19a1tm1Toda
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased ovary apoptosis
|
J:70359
|
Cyp26b1tm1.1Ptk/Cyp26b1tm1.1Ptk
(involves: 129S2/SvPas)
|
abnormal male germ cell apoptosis
|
J:126705
|
decreased male germ cell number
|
J:126705
|
Cyp26b1tm1Dcp/Cyp26b1tm1Dcp
(involves: 129S4/SvJae * C57BL/6)
|
abnormal male meiosis
|
J:215225
|
Cyp26b1tm1Hmd/Cyp26b1tm1Hmd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal apoptosis
|
J:89029
|
Cyp26b1tm1Ptk/Cyp26b1tm1Ptk Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal male meiosis
|
J:154048
|
decreased male germ cell number
|
J:154048
|
Cyp27b1tm1Star/Cyp27b1tm1Star
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:89330
|
Cyrenem1Vokh/Cyrenem1Vokh
(C57BL/6-Cyrenem1Vokh)
|
decreased neuronal precursor proliferation
|
J:306598
|
Cyrentm1.1(KOMP)Vlcg/Cyrentm1.1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
increased cellular sensitivity to ionizing radiation
|
J:265834
|
Cyrentm1.1(KOMP)Vlcg/Cyrentm1.1(KOMP)Vlcg Nhej1tm1Fwa/Nhej1tm1Fwa
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
increased neuron apoptosis
|
J:265834
|
Cyribm1Ivdi/Cyribm1Ivdi
(involves: 129S1/Sv * 129X1/SvJ * DBA/2J)
|
abnormal large intestine goblet cell morphology
|
J:282597
|
Cyribtm1c(KOMP)Wtsi/Cyribtm1d(KOMP)Wtsi Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * BcA17/Skmn * C57BL/6N)
|
abnormal actin cytoskeleton morphology
|
J:282597
|
Cysltr1tm1Ykn/Cysltr1tm1Ykn
(involves: C57BL/6)
|
abnormal cell physiology
|
J:77087
|
Cytiptm1Tes/Cytiptm1Tes
(involves: 129S1/Sv * FVB/N)
|
abnormal cellular extravasation
|
J:110320
|
abnormal leukocyte migration
|
J:110320
|
D130043K22Riktm1b(KOMP)Wtsi/D130043K22Rik+
(involves: C57BL/6 * CBA)
|
cellular phenotype
|
J:241324
|
D130043K22Riktm1b(KOMP)Wtsi/D130043K22Riktm1b(KOMP)Wtsi
(involves: C57BL/6 * CBA)
|
cellular phenotype
|
J:241324
|
Daam1Gt(RRT390)Byg/Daam1Gt(RRT390)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell adhesion
|
J:167714
|
abnormal fibroblast physiology
|
J:167714
|
Dab1tm1.1Mull/Dab1tm1.1Mull
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal neuronal migration
|
J:174747
|
Dab1tm1.1Mull/Dab1tm1.1Mull Cux2tm2.1(cre)Mull/Cux2+
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL)
|
abnormal neuronal migration
|
J:174747
|
Dab1tm1.1Mull/Dab1tm1.1Mull Neurod6tm1(cre)Kan/Neurod6+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuronal migration
|
J:174747
|
Dab1tm1.1Mull/Dab1tm1.1Mull Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL)
|
abnormal neuronal migration
|
J:174747
|
Dab1tm1Cpr/Dab1tm1Cpr
(either: (involves: 129S4/SvJaeSor * BALB/c) or (involves: 129S4/SvJaeSor * C57BL/6))
|
abnormal neuronal precursor cell migration
|
J:121846
|
Dab1tm1Cpr/Dab1tm3.1Cpr
(involves: 129S4/SvJaeSor * C57BL/6J)
|
abnormal neuronal migration
|
J:74239
|
Dab2tm1.1Cpr/Dab2tm1.1Cpr
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:75911
|
Dab2tm1Xxx/Dab2tm1Xxx
(involves: 129S6/SvEvTac * C57BL/6)
|
absent inner cell mass proliferation
|
J:79862
|
Dab2iptm1.1Wami/Dab2iptm1.1Wami
(involves: 129 * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:136554
|
Dach1tm1Krs/Dach1tm1Krs
(involves: 129P2/OlaHsd)
|
decreased pancreatic beta cell proliferation
|
J:166952
|
Dact2tm1.1Xya/Dact2tm1.1Xya
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased keratinocyte migration
|
J:139684
|
Dad1tm1Brw/Dad1+
(involves: 129P2/OlaHsd * Black Swiss)
|
increased embryonic tissue cell apoptosis
|
J:62083
|
Dad1tm1Brw/Dad1tm1Brw
(involves: 129P2/OlaHsd * Black Swiss)
|
abnormal inner cell mass apoptosis
|
J:62083
|
Dad1tm1Wnt/Dad1tm1Wnt
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:77517
|
increased embryonic tissue cell apoptosis
|
J:77517
|
Dag1tm1Kcam/Dag1tm2.1Kcam Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal axon fasciculation
|
J:194150
|
abnormal axon guidance
|
J:194150
|
abnormal basement membrane morphology
|
J:194150
|
radial glial endfoot detachment
|
J:194150
|
Dag1tm1Kcam/Dag1tm2Kcam Tg(GFAP-cre)25Mes/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal neuronal migration
|
J:86901
|
Dag1tm2Kcam/Dag1tm2Kcam Tg(GFAP-cre)25Mes/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal neuronal migration
|
J:86901
|
Daglatm1Pado/Dagla+
(C57BL/6-Daglatm1Pado)
|
abnormal neuron proliferation
|
J:157850
|
Daglatm1Pado/Daglatm1Pado
(C57BL/6-Daglatm1Pado)
|
abnormal neuron proliferation
|
J:157850
|
DaglbGt(OST195261)Lex/Daglb+
(B6.129S5-DaglbGt(OST195261)Lex)
|
abnormal neuron proliferation
|
J:157850
|
DaglbGt(OST195261)Lex/DaglbGt(OST195261)Lex
(B6.129S5-DaglbGt(OST195261)Lex)
|
abnormal neuron proliferation
|
J:157850
|
Dap3Gt(OST147863)Lex/Dap3Gt(OST147863)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal mitochondrial morphology
|
J:129756
|
decreased fibroblast apoptosis
|
J:129756
|
Dapk1Gt(IST12766D5)Tigm/Dapk1Gt(IST12766D5)Tigm
(C57BL/6-Dapk1Gt(IST12766D5)Tigm)
|
decreased neuron apoptosis
|
J:161179
|
Dapk1tm1Akc/Dapk1tm1Akc
(B6.129X1-Dapk1tm1Akc)
|
decreased renal tubule apoptosis
|
J:158109
|
decreased sensitivity to induced cell death
|
J:158109
|
Dapk1tm1Akc/Dapk1tm1Akc Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrj)
|
abnormal cell morphology
|
J:158109
|
Dapk1tm1Yuk/Dapk1tm1Yuk
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased renal tubule apoptosis
|
J:92102
|
Dapl1em1Nju/Dapl1em1Nju
(C57BL/6J-Dapl1em1Nju)
|
increased cell proliferation
|
J:242244
|
Dapp1Gt(OST111213)Lex/Dapp1Gt(OST111213)Lex
(B6.Cg-Dapp1Gt(OST111213)Lex)
|
decreased B cell proliferation
|
J:110009
|
Dapp1tm1Mnz/Dapp1tm1Mnz
(B6.129P2-Dapp1tm1Mnz)
|
decreased B cell proliferation
|
J:86182
|
Daw1b2b1116Clo/Daw1b2b1116Clo
(C57BL/6J-Daw1b2b1116Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
immotile respiratory cilia
|
J:175213
|
Daxxtm1Led/Daxxtm1Led
(involves: 129S6/SvEvTac * Black Swiss)
|
increased allantois apoptosis
|
J:56796
|
increased embryonic neuroepithelium apoptosis
|
J:56796
|
increased embryonic tissue cell apoptosis
|
J:56796
|
Daxxtm1Maul/Daxxtm1Maul
(involves: 129)
|
binucleate
|
J:91881
|
Dazap1tm1Pyen/Dazap1tm1Pyen
(involves: 129S6/SvEvTac)
|
abnormal spermatocyte morphology
|
J:171493
|
abnormal spermatogonia proliferation
|
J:171493
|
multinucleated giant male germ cells
|
J:171493
|
Dazltm1Hjc/Dazl+
(involves: 129P2/OlaHsd * MF1)
|
abnormal male germ cell morphology
|
J:42612
|
oligozoospermia
|
J:42612
|
Dbf/Dbf+
(involves: 101/H * C3H/HeH)
|
oligozoospermia
|
J:39106
|
dblr/dblr
(involves: C57BL/6J * SJL/J)
|
abnormal apoptosis
|
J:82633
|
DbnlGt(betageo)11Byg/DbnlGt(betageo)11Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:119847
|
Dcaf1tm1.1Yxi/Dcaf1tm1.2Yxi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle
|
J:140246
|
decreased fibroblast proliferation
|
J:140246
|
increased fibroblast apoptosis
|
J:140246
|
Dcaf8em1Rbren/Dcaf8em1Rbren
(Not Specified)
|
abnormal sperm head morphology
|
J:307635
|
decreased sperm progressive motility
|
J:307635
|
Dcaf13em2Hyfn/Dcaf13em2Hyfn Tg(Gdf9-icre)5092Coo/0
(involves: C57BL/6)
|
abnormal cell physiology
|
J:302700
|
abnormal oocyte morphology
|
J:302700
|
abnormal translation
|
J:302700
|
absent oocytes
|
J:302700
|
Dcaf13em2Hyfn/Dcaf13em2Hyfn Tg(Zp3-cre)93Knw/0
(involves: C57BL/6 * C57BL/6J)
|
abnormal oocyte morphology
|
J:302700
|
Dcaf17tm1.1Assi/Dcaf17tm1.1Assi
(involves: 129S6/SvEvTac * BALB/cJ * C57BL/6NTac)
|
abnormal acrosome assembly
|
J:262620
|
abnormal acrosome morphology
|
J:262620
|
abnormal male meiosis
|
J:262620
|
abnormal manchette morphology
|
J:262620
|
abnormal manchette perinuclear ring morphology
|
J:262620
|
abnormal sperm flagellum morphology
|
J:262620
|
abnormal sperm head morphology
|
J:262620
|
abnormal sperm midpiece morphology
|
J:262620
|
abnormal sperm nucleus morphology
|
J:262620
|
asthenozoospermia
|
J:262620
|
detached acrosome
|
J:262620
|
elongated manchette
|
J:262620
|
globozoospermia
|
J:262620
|
increased male germ cell apoptosis
|
J:262620
|
oligozoospermia
|
J:262620
|
teratozoospermia
|
J:262620
|
Dcbld2tm1.1Mhms/Dcbld2tm1.1Mhms
(B6.129S6-Dcbld2tm1.1Mhms)
|
decreased lung endothelial cell migration
|
J:207629
|
decreased lung endothelial cell proliferation
|
J:207629
|
Dcckanga/Dcckanga
(involves: AKR * C3H)
|
abnormal axon guidance
|
J:80430
|
Dcckanga/Dcctm1Wbg
(involves: 129X1/SvJ * AKR * C3H)
|
abnormal axon guidance
|
J:80430
|
Dcctm1.1Mehl/Dcctm1.1Mehl
(Not Specified)
|
decreased enterocyte apoptosis
|
J:181517
|
decreased fibroblast apoptosis
|
J:181517
|
Dcctm1Nki/Dcctm1Nki Trp53tm1Brn/Trp53tm1Brn Tg(KRT14-cre)8Brn/?
(involves: 129P2/OlaHsd * FVB/N)
|
decreased apoptosis
|
J:181090
|
Dcctm1Wbg/Dcc+ Unc5crcmTg(Ucp)1.23Kz/Unc5c+
(involves: 129X1/SvJ * C57BL/6J * SJL/J)
|
abnormal axon guidance
|
J:80430
|
Dcctm1Wbg/Dcc+ Unc5crcmTg(Ucp)1.23Kz/Unc5crcmTg(Ucp)1.23Kz
(involves: 129X1/SvJ * C57BL/6J * SJL/J)
|
abnormal axon guidance
|
J:80430
|
Dcctm1Wbg/Dcctm1Wbg
(involves: 129S2/SvPas)
|
abnormal axon guidance
|
J:39765
|
Dckmemi/Dckmemi
(C57BL/6J-Dckmemi)
|
increased T cell apoptosis
|
J:184080
|
increased T cell proliferation
|
J:184080
|
Dclk1tm1.1Jgg/Dclk1tm1.1Jgg
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6)
|
abnormal axon guidance
|
J:105300
|
Dclre1atm1Remo/Dclre1atm1Remo
(involves: 129X1/SvJ)
|
abnormal chromosome morphology
|
J:134461
|
Dclre1atm1Rleg/Dclre1atm1Rleg
(involves: 129S7/SvEvBrd)
|
decreased cell proliferation
|
J:102381
|
Dclre1atm1Roka/Dclre1atm1Roka
(Not Specified)
|
abnormal cell physiology
|
J:62832
|
Dclre1ctm1Fwa/Dclre1ctm1Fwa
(involves: 129S6/SvEvTac * C57BL/6)
|
chromosomal instability
|
J:80995
|
increased cellular sensitivity to ionizing radiation
|
J:80995
|
Dclre1ctm1Fwa/Dclre1ctm1Fwa
(involves: 129S6/SvEvTac)
|
increased cellular sensitivity to gamma-irradiation
|
J:147864
|
induced chromosome breakage
|
J:147864
|
Dclre1ctm1Jsek/Dclre1ctm1Jsek
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:147864
|
induced chromosome breakage
|
J:147864
|
Dclre1ctm2Mcow/Dclre1ctm2Mcow
(involves: 129/Sv * C57BL/6)
|
abnormal cell physiology
|
J:96535
|
decreased B cell proliferation
|
J:96535
|
decreased T cell proliferation
|
J:96535
|
increased cellular sensitivity to ionizing radiation
|
J:96535
|
Dcntm1Ioz/Dcntm1Ioz
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss)
|
increased renal tubule apoptosis
|
J:75298
|
Dcp2tm1Smoc/Dcp2tm1Smoc Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
(involves: 129S/SvEv * C57BL/6)
|
asthenozoospermia
|
J:292283
|
decreased male germ cell number
|
J:292283
|
increased male germ cell apoptosis
|
J:292283
|
Dcstamptm1Suda/Dcstamptm1Suda
(Not Specified)
|
abnormal osteoclast differentiation
|
J:100555
|
Dctn1tm1.1Cai/Dctn1tm1.1Cai
(involves: 129X1/SvJ * C57BL/6 * FVB/N)
|
increased apoptosis
|
J:129269
|
Dctn1tm1Cai/Dctn1tm1Cai
(involves: 129X1/SvJ * C57BL/6 * FVB/N)
|
increased apoptosis
|
J:129269
|
Dctn1tm2.1Cai/Dctn1tm2.1Cai Tg(Thy1-cre)1Vln/?
(involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * FVB/N)
|
increased susceptibility to neuronal excitotoxicity
|
J:264431
|
lysosomal protein accumulation
|
J:264431
|
Dcun1d1Gt(RRR261)Byg/Dcun1d1Gt(RRR261)Byg
(involves: 129P2/OlaHsd)
|
abnormal sperm flagellum morphology
|
J:270036
|
abnormal sperm head morphology
|
J:270036
|
asthenozoospermia
|
J:270036
|
decreased fibroblast proliferation
|
J:262901
|
globozoospermia
|
J:270036
|
oligozoospermia
|
J:270036
|
teratozoospermia
|
J:270036
|
Ddb1tm1Spg/Ddb1tm1Spg Plekha5Tg(AMH-cre)1Flor/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
oligozoospermia
|
J:291677
|
Ddb1tm1Spg/Ddb1tm1Spg Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal neuron apoptosis
|
J:117820
|
increased lens epithelium apoptosis
|
J:117820
|
Ddb2tm1Linn/Ddb2tm1Linn
(involves: 129S/SvEv * C57BL/6)
|
decreased cellular sensitivity to ionizing radiation
|
J:88125
|
Ddctm1.1Rhrs/Ddctm1.1Rhrs Tg(Ggt1-cre)M3Egn/0
(involves: 129 * C57BL/6 * SJL)
|
oxidative stress
|
J:175630
|
Ddctm1.1Rhrs/Ddctm1.1Rhrs Tg(Ggt1-cre)M3Egn/0
(129.Cg-Ddctm1.1Rhrs Tg(Ggt1-cre)M3Egn)
|
oxidative stress
|
J:175630
|
dde/dde
(CByJ(Cg)-dde/GrsrJ)
|
abnormal male germ cell apoptosis
|
J:159016
|
Ddhd1tm1.1Katn/Ddhd1tm1.1Katn
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal sperm annulus morphology
|
J:212425
|
abnormal sperm mitochondrial sheath morphology
|
J:212425
|
asthenozoospermia
|
J:212425
|
decreased sperm mitochondrial sheath size
|
J:212425
|
hairpin sperm flagellum
|
J:212425
|
kinked sperm flagellum
|
J:212425
|
oligozoospermia
|
J:212425
|
teratozoospermia
|
J:212425
|
Ddiastm1Enik/Ddiastm1Enik
(Not Specified)
|
decreased male germ cell number
|
J:123623
|
decreased round spermatid number
|
J:123623
|
increased cellular sensitivity to DNA damaging agents
|
J:123623
|
increased cellular sensitivity to gamma-irradiation
|
J:123623
|
increased cellular sensitivity to hydrogen peroxide
|
J:123623
|
increased cellular sensitivity to ultraviolet irradiation
|
J:123623
|
increased fibroblast apoptosis
|
J:123623
|
increased sensitivity to induced cell death
|
J:123623
|
Ddit3tm1Aki/Ddit3tm1Aki
(involves: 129P2/OlaHsd)
|
decreased neuron apoptosis
|
J:109623
|
Ddit3tm1Aki/Ddit3tm1Aki
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased apoptosis
|
J:76277
|
Ddit3tm1Dron/Ddit3tm1Dron
(either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
decreased apoptosis
|
J:52729
|
decreased fibroblast apoptosis
|
J:52729
|
Ddit3tm1Dron/Ddit3tm1Dron
(B6.129-Ddit3tm1Dron)
|
decreased macrophage apoptosis
|
J:153833
|
Ddit4tm1Fein/Ddit4tm1Fein
(involves: 129S5/SvEvBrd * C57BL/6)
|
decreased retina apoptosis
|
J:93450
|
Ddit4tm1Lwe/Ddit4tm1Lwe
(involves: 129S4/SvJae)
|
abnormal cell morphology
|
J:99368
|
Ddr1tm1Wfv/Ddr1tm1Wfv
(either: (involves: (129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
increased mammary gland epithelial cell proliferation
|
J:68368
|
Ddr2slie/Ddr2slie
(BKSChpLt.Cg-Tg(Ins2-Cpe)1Lt Cpefat/LtJng)
|
abnormal spermatogonia morphology
|
J:134371
|
decreased spermatid number
|
J:134371
|
Ddr2tm1Kln/Ddr2tm1Kln
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:74580
|
Ddrgk1tm1b(EUCOMM)Hmgu/Ddrgk1tm1b(EUCOMM)Hmgu
(involves: C57BL/6N)
|
increased cell death
|
J:231701
|
Ddx3xtm1.1Lyou/Y Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129 * C57BL/6 * CBA)
|
abnormal cell cycle
|
J:231798
|
abnormal cell physiology
|
J:231798
|
increased embryonic tissue cell apoptosis
|
J:231798
|
increased mitotic index
|
J:231798
|
Ddx4tm1Tnc/Ddx4+
(involves: 129P2/OlaHsd * C57BL/6NJcl)
|
abnormal primordial germ cell migration
|
J:61665
|
decreased primordial germ cell number
|
J:61665
|
Ddx4tm1Tnc/Ddx4tm1Tnc
(involves: 129P2/OlaHsd * C57BL/6NJcl)
|
abnormal primordial germ cell migration
|
J:61665
|
arrest of male meiosis
|
J:61665
|
decreased primordial germ cell number
|
J:61665
|
decreased primordial germ cell proliferation
|
J:61665
|
increased male germ cell apoptosis
|
J:61665
|
Ddx4tm1Tnc/Ddx4tm1Tnc
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal oocyte morphology
|
J:115333
|
abnormal spermatocyte morphology
|
J:115333
|
arrest of male meiosis
|
J:115333
|
Ddx5tm1.1Arte/Ddx5tm1.1Arte Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: C57BL/6N * C57BL/6NTac)
|
increased cellular sensitivity to gamma-irradiation
|
J:191933
|
Ddx5tm1.1Arte/Ddx5tm1.1Arte Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6NTac * FVB)
|
abnormal male germ cell physiology
|
J:306880
|
azoospermia
|
J:306880
|
decreased male germ cell number
|
J:306880
|
Ddx6em1.1Ysa/Ddx6em1.1Ysa Tg(Ddx4-cre)1Dcas/0
(involves: 129S4/SvJaeSor * C57BL/6NCrlj * CBA/JNCrlj * FVB)
|
absent oocytes
|
J:282136
|
Ddx11cetus/Ddx11cetus
(either: C3Fe.B6-Ddx11cetus or (involves: C3HeB/FeJ * C57BL/6J * CAST/Ei))
|
increased embryonic tissue cell apoptosis
|
J:185600
|
Ddx11tm1Jiml/Ddx11tm1Jiml
(involves: 129S/SvEv)
|
abnormal cell cycle
|
J:158490
|
aneuploidy
|
J:158490
|
decreased inner cell mass proliferation
|
J:158490
|
increased allantois apoptosis
|
J:158490
|
increased embryonic tissue cell apoptosis
|
J:185600,
J:158490
|
Ddx25tm1Mld/Ddx25+
(involves: 129S4/SvJae)
|
abnormal apoptosis
|
J:89546
|
Ddx25tm1Mld/Ddx25tm1Mld
(involves: 129S4/SvJae)
|
increased male germ cell apoptosis
|
J:89546
|
Ddx39bem1Cya/Ddx39b+
(C57BL/6N-Ddx39bem1Cya/Cya)
|
increased cellular sensitivity to gamma-irradiation
|
J:299665
|
Def6Gt(OST307148)Lex/Def6Gt(OST307148)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
decreased T cell apoptosis
|
J:106469
|
Degs1Gt(OST368559)Lex/Degs1+
(involves: 129S5/SvEvBrd)
|
increased muscle cell glucose uptake
|
J:203554
|
Del(1)1Brk/Del(1)1Brk
(involves: 129S6/SvEvTac * C57BL/6J * CBA/J)
|
abnormal respiratory motile cilium physiology
|
J:130396
|
absent sperm flagellum
|
J:130396
|
azoospermia
|
J:130396
|
Del(1Aim2-Ifi205)1Stsn/Del(1Aim2-Ifi205)1Stsn
(B6(129S4)-Del(1Aim2-Ifi205)1Stsn)
|
decreased macrophage apoptosis
|
J:234263
|
Del(2Cd59b-Cd59a)1Jha/Del(2Cd59b-Cd59a)1Jha
(B6.129-Del(2Cd59b-Cd59a)1Jha)
|
oligozoospermia
|
J:170754
|
Del(2Dlx1-Dlx2)1Jlr/Del(2Dlx1-Dlx2)1Jlr
(involves: 129X1/SvJ)
|
impaired neuronal migration
|
J:41860
|
Del(2Hoxd4-Hoxd11)36Ddu/Del(2Hoxd4-Hoxd11)36Ddu
(Not Specified)
|
increased kidney apoptosis
|
J:131874
|
increased renal tubule apoptosis
|
J:131874
|
Del(2Hoxd4-Hoxd13)30Ddu/Del(2Hoxd4-Hoxd13)30Ddu
(involves: 129S2/SvPas)
|
increased kidney apoptosis
|
J:131874
|
increased renal tubule apoptosis
|
J:131874
|
Del(2Hoxd11-Hoxd13)29Ddu/Del(2Hoxd11-Hoxd13)29Ddu
(involves: 129S2/SvPas)
|
abnormal interdigital cell death
|
J:36443
|
Del(2Nespas-Gnas)1Hju/+
(either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J))
|
abnormal DNA methylation
|
J:160293
|
abnormal imprinting
|
J:160293
|
maternal imprinting
|
J:160293
|
Del(3Bglap2-Bglap)2Kry/Del(3Bglap2-Bglap)2Kry
(involves: 129S7/SvEvBrd)
|
abnormal spermatocyte morphology
|
J:170888
|
decreased adipocyte glucose uptake
|
J:126780
|
decreased pancreatic beta cell proliferation
|
J:126780
|
decreased spermatid number
|
J:170888
|
oligozoospermia
|
J:170888
|
Del(4C4-C5)1Lap/Del(4C4-C5)1Lap
(involves: 129S6/SvEvTac)
|
delayed cellular replicative senescence
|
J:158126
|
increased fibroblast proliferation
|
J:158126
|
increased vascular smooth muscle cell proliferation
|
J:158126
|
Del(4D4Mit190-D4Mit51)2Aam/+
(involves: 129S7/SvEvBrd)
|
abnormal mitosis
|
J:121726
|
delayed cellular replicative senescence
|
J:121726
|
increased fibroblast proliferation
|
J:121726
|
Del(5Kit-Cep135)1Utr/Del(5Kit-Cep135)1Utr
(C57BL/6JCrlj-Del(5Kit-Cep135)1Utr)
|
decreased inner cell mass proliferation
|
J:233978
|
Del(6Ephb6-Trpv6)2Mfre/Del(6Ephb6-Trpv6)2Mfre
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)
|
asthenozoospermia
|
J:185629
|
necrospermia
|
J:185629
|
Del(6Spam1-Hyal5)1Eki/Del(6Spam1-Hyal5)1Eki
(Not Specified)
|
abnormal sperm motility
|
J:294353
|
Del(7)Tyrc-3H/Del(7)Tyrc-6H
(involves: 101/H * C3H/HeH)
|
abnormal male germ cell morphology
|
J:6034
|
abnormal sperm nucleus morphology
|
J:6034
|
maternal effect
|
J:6034
|
Del(7Gabrb3-Ube3a)1Yhj/+
(B6.129S7-Del(7Gabrb3-Ube3a)1Yhj)
|
paternal imprinting
|
J:164010
|
Del(7Herc2-Mkrn3)13FRdni/+
(involves: C57BL/6 * CD-1 * SJL)
|
maternal imprinting
|
J:56614
|
Del(7Ins2-Tel)1Lef/+
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
paternal imprinting
|
J:130399
|
Del(7Ipw-Snord116)1Jbro/+
(involves: 129S7/SvEvBrd * C57BL/6)
|
maternal imprinting
|
J:242655
|
Del(7Slx1b-Sept1)4Aam/0
(B6129S-Del(7Slx1b-Sept1)4Aam/J)
|
decreased radial glial cell number
|
J:219859
|
increased neuronal precursor proliferation
|
J:219859
|
Del(8Col4a1-Col4a2)1Epo/Del(8Col4a1-Col4a2)1Epo
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal basement membrane morphology
|
J:89190
|
abnormal neuronal migration
|
J:89190
|
impaired basement membrane formation
|
J:89190
|
Del(8Defb1-Defb13)1Jrdo/Del(8Defb1-Defb13)1Jrdo
(involves: 129P2/OlaHsd * C57BL/6N)
|
abnormal sperm axoneme morphology
|
J:204187
|
asthenozoospermia
|
J:204187
|
decreased sperm progressive motility
|
J:204187
|
detached sperm flagellum
|
J:204187
|
Del(9Apoa1-Apoa4)1Hmez/Del(9Apoa1-Apoa4)1Hmez
(involves: 129P2/OlaHsd * C57BL/6)
|
increased macrophage derived foam cell number
|
J:109005
|
Del(10Grin3b-Tmem259)1Zang/Del(10Grin3b-Tmem259)1Zang
(involves: 129X1/SvJ * C57BL/6)
|
increased endoplasmic reticulum stress
|
J:185796
|
Del(11Cops3-Rnf112)1Jrl/+
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal sperm flagellum morphology
|
J:83302
|
oligozoospermia
|
J:83302
|
Del(11Cxcl16-Zmynd15)1Ifc/Del(11Cxcl16-Zmynd15)1Ifc
(involves: 129S4/SvJae * C57BL/6)
|
azoospermia
|
J:166802
|
increased male germ cell apoptosis
|
J:166802
|
Del(11Cxcl16-Zmynd15)1Ifc/Del(11Cxcl16-Zmynd15)1Ifc Ldlrtm1Her/Ldlrtm1Her
(B6.129S-Ldlrtm1Her Del(11Cxcl16-Zmynd15)1Ifc)
|
increased apoptosis
|
J:123851
|
Del(11Jmjd6-Mettl23)1Ysfk/Del(11Jmjd6-Mettl23)1Ysfk
(involves: C57BL/6)
|
abnormal apoptosis
|
J:90288
|
impaired macrophage chemotaxis
|
J:90288
|
impaired macrophage phagocytosis
|
J:90288
|
Del(13)1N/Del(13)1N
(C57BL/6N)
|
abnormal DNA-templated transcription
|
J:282526
|
abnormal epigenetic regulation of gene expression
|
J:282526
|
Del(13Zfp997-Vmn2r-ps103)1Aiwsk/Del(13Zfp997-Vmn2r-ps103)1Aiwsk Zfp998em1Aiwsk/Zfp998em1Aiwsk
(involves: C57BL/6J)
|
abnormal DNA-templated transcription
|
J:282526
|
abnormal epigenetic regulation of gene expression
|
J:282526
|
Del(14Ltb4r2-Ltb4r1)1Bodd/Del(14Ltb4r2-Ltb4r1)1Bodd
(involves: 129S4/SvJaeSor * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:163271
|
Del(14Prss51-Prss55)3Osb/Del(14Prss51-Prss55)3Osb
(involves: C57BL/6J * DBA/2J)
|
impaired sperm migration in female genital tract
|
J:293896
|
Del(14Trim13-Dleu2)4Rdf/Del(14Trim13-Dleu2)4Rdf
(involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6)
|
abnormal B cell proliferation
|
J:156946
|
Del(15Krt7-Krt18)1Tmm/Del(15Krt7-Krt18)1Tmm
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:153804
|
Del(16Dgcr2-Hira)1Rak/+
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL)
|
patent ductus arteriosus
|
J:67796
|
Del(16Dppa4-Dppa2)1Reik/+
(involves: C57BL/6 * FVB/N)
|
maternal effect
|
J:316936
|
Del(16Es2el-Ufd1l)217Bld/+
(B6.129S7-Del(16Es2el-Ufd1l)217Bld)
|
abnormal neuron proliferation
|
J:201966
|
abnormal neuronal migration
|
J:201966
|
Del(16Hspa13-App)3Yah/+
(B6J.129P2-Del(16Hspa13-App)3Yah)
|
abnormal cellular respiration
|
J:223518
|
abnormal mitochondrial physiology
|
J:223518
|
increased mitochondrial DNA content
|
J:223518
|
Del(16Lipi-Usp25)1Dja/Del(16Lipi-Usp25)1Dja
(involves: 129P2/OlaHsd * C57BL/6)
|
increased neural tube apoptosis
|
J:184302
|
Del(16Tssk1-Tssk2)1Agr/Del(16Tssk1-Tssk2)1Agr
(B6.129S5(Cg)-Del(16Tssk1-Tssk2)1Agr)
|
asthenozoospermia
|
J:156758
|
oligozoospermia
|
J:156758
|
teratozoospermia
|
J:156758
|
Del(16Tssk1-Tssk2)1Joch/+
(chimera involves: 129X1/SvJ)
|
azoospermia
|
J:137707
|
decreased elongated spermatid number
|
J:137707
|
Del(17)Thp/+
(involves: AKR/J * C57BL/Gr * CBA/Gr)
|
maternal effect
|
J:31524
|
Del(17Fpr1-Fpr2)1Jimw/Del(17Fpr1-Fpr2)1Jimw
(Not Specified)
|
abnormal enterocyte proliferation
|
J:197568
|
Del(17Hspa1b-Hsp1a)1Dix/Del(17Hspa1b-Hsp1a)1Dix
(involves: 129S7/SvEvBrd)
|
abnormal cell cycle checkpoint function
|
J:87581
|
abnormal cell physiology
|
J:87581
|
abnormal DNA repair
|
J:87581
|
abnormal spermatocyte morphology
|
J:87581
|
decreased cell proliferation
|
J:87581
|
decreased mitotic index
|
J:87581
|
early cellular replicative senescence
|
J:87581
|
increased cellular sensitivity to gamma-irradiation
|
J:87581
|
induced chromosome breakage
|
J:87581
|
spontaneous chromosome breakage
|
J:87581
|
Del(17Trem1-Trem3)1Jkt/Del(17Trem1-Trem3)1Jkt
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:194295
|
Del(18Pcdhg)1Xzw/Del(18Pcdhg)1Xzw
(Not Specified)
|
increased neuron apoptosis
|
J:188341
|
increased spinal cord apoptosis
|
J:107735
|
Del(19Cyp26a1-Cyp26c1)1Hmd/Del(19Cyp26a1-Cyp26c1)1Hmd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal neural crest cell migration
|
J:119939
|
Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt
(involves: 129P2/OlaHsd)
|
abnormal ependyma motile cilium morphology
|
J:75779
|
abnormal respiratory motile cilium morphology
|
J:75779
|
asthenozoospermia
|
J:75779
|
cellular phenotype
|
J:75779
|
decreased elongated spermatid number
|
J:75779
|
globozoospermia
|
J:75779
|
teratozoospermia
|
J:75779
|
Del(MTmt-Tk-mt-Nd5)1Jiha
(involves: C57BL/6J * CBA * DBA/2)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:65025
|
Del(MTmt-Tk-mt-Nd5)1Jiha
(involves: C57BL/6J * CBA)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:115155,
J:103743,
J:72614,
J:92536,
J:132407
|
abnormal mitochondrial crista morphology
|
J:72614
|
abnormal sperm midpiece morphology
|
J:115155
|
abnormal sperm nucleus morphology
|
J:115155
|
absent sperm head
|
J:115155
|
arrest of male meiosis
|
J:115155
|
asthenozoospermia
|
J:115155
|
decreased germ cell number
|
J:115155
|
dilated mitochondrion
|
J:72614
|
oligozoospermia
|
J:115155
|
teratozoospermia
|
J:115155
|
Del(MTmt-Tk-mt-Nd5)1Jiha
(involves: C57BL/6JJcl * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal oxidative phosphorylation
|
J:199416
|
Del(XMagea1-Magea6)1Nju/Y Tg(EIIa-cre)C5379Lmgd/0
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N)
|
increased cellular sensitivity to DNA damaging agents
|
J:240206
|
increased male germ cell apoptosis
|
J:240206
|
oligozoospermia
|
J:240206
|
Del(XMagea6-Magea1)1Prp/Y
(involves: C57BL/6)
|
oligozoospermia
|
J:342299
|
X/Del(Y)1H Tg(Sry)2Ei/0
(involves: MF1)
|
abnormal sperm head morphology
|
J:89312
|
X/Del(Y)1Psb
(Not Specified)
|
abnormal sperm head morphology
|
J:155571
|
X/Del(Y)1PsbSrydl1Rlb Tg(Sry)2Ei/0
(involves: 129S6/SvEvTac * MF1)
|
abnormal acrosome morphology
|
J:89616
|
Del(Y)2H/?
(mixed)
|
abnormal chromosomal synapsis
|
J:15425
|
arrest of male meiosis
|
J:15425
|
Del(Y)3H/?
(mixed)
|
abnormal chromosomal synapsis
|
J:15425
|
arrest of male meiosis
|
J:15425
|
X/Del(YRIII)2Psb
(involves: RIII)
|
abnormal sperm head morphology
|
J:155571
|
X/Del(YRIII)2Psb
(C57BL/10-Del(YRIII)2Psb)
|
abnormal spermatid morphology
|
J:17614
|
X/Del(YRIII)2Psb Tg(CAG-EGFP,RNU6-RNAi:Sly)367Psb/0
(involves: C57BL/10 * CBA/Ca * MF1 * RIII)
|
abnormal sperm head morphology
|
J:155571
|
Dennd1aem1Jgfu/Dennd1aem1Jgfu
(Not Specified)
|
abnormal primordial germ cell migration
|
J:276703
|
decreased apoptosis
|
J:276703
|
decreased cell proliferation
|
J:276703
|
decreased hepatocyte proliferation
|
J:276703
|
increased apoptosis
|
J:276703
|
Derl2tm1.2Hpl/Derl2tm1.2Hpl
(involves: BALB/cJ)
|
abnormal cell physiology
|
J:170650
|
Destm1.1Ccrs/Destm1.1Ccrs
(involves: 129 * C57BL/6J)
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:219616
|
increased mitochondrial size
|
J:219616
|
Destm1Cap/Destm1Cap
(involves: 129S7/SvEvBrd * C57BL/6)
|
cardiac interstitial fibrosis
|
J:35123
|
Destm1Cap/Destm1Cap Tg(Bcl2)ACap/Tg(Bcl2)ACap
(involves: 129S7/SvEvBrd * C57BL/6)
|
cardiac interstitial fibrosis
|
J:88267
|
Destm1Cap/Destm1Cap Tg(Bcl2)BCap/Tg(Bcl2)BCap
(involves: 129S7/SvEvBrd * C57BL/6)
|
cardiac interstitial fibrosis
|
J:88267
|
Destm1Cba/Destm1Cba Synmtm1.1Ics/Synmtm1.1Ics
(involves: 129S2/SvPas)
|
abnormal myoblast differentiation
|
J:268425
|
Dffatm1Mxu/Dffatm1Mxu
(involves: 129S4/SvJae * C57BL/6)
|
abnormal apoptosis
|
J:50707,
J:88144
|
decreased susceptibility to neuronal excitotoxicity
|
J:114416
|
Dffatm1Mxu/Dffatm1Mxu Endog/D2Wsu81etm1Mxu/Endog+
(involves: 129 * C57BL/6)
|
decreased apoptosis
|
J:88144
|
Dffbtm1Osa/Dffbtm1Osa
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal apoptosis
|
J:81474
|
Dgat1tm1Far/Dgat1tm1Far
(B6J.129S4-Dgat1tm1Far)
|
decreased mammary gland epithelial cell proliferation
|
J:128259
|
Dgcr8Gt(XG058)Byg/Dgcr8+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:198659
|
Dgcr8Gt(XG058)Byg/Dgcr8+
(B6.129P2-Dgcr8Gt(XG058)Byg)
|
abnormal neuronal migration
|
J:201966
|
Dgkztm1Gak/Dgkztm1Gak
(involves: 129X1/SvJ * C57BL/6)
|
increased T cell proliferation
|
J:85149
|
Dguoktm1.1Anka/Dguoktm1.1Anka
(involves: 129 * C57BL/6N)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:294620
|
abnormal mitochondrial crista morphology
|
J:294620
|
abnormal mitochondrial shape
|
J:294620
|
abnormal redox activity
|
J:294620
|
decreased hepatocyte mitochondrial DNA content
|
J:294620
|
decreased mitochondrial DNA content
|
J:294620
|
decreased myocardial fiber mitochondrial DNA content
|
J:294620
|
decreased skeletal muscle fiber mitochondrial DNA content
|
J:294620
|
dilated mitochondrion
|
J:294620
|
increased hepatocyte karyomegaly
|
J:294620
|
increased hepatocyte proliferation
|
J:294620
|
oxidative stress
|
J:294620
|
Dh/Dh+ H2d/H2d
(NZB.Cg-Dh)
|
decreased B cell proliferation
|
J:12036
|
increased T cell proliferation
|
J:12036
|
Dhfrorana/Dhfrorana
(involves: C57BL/6JAnu)
|
abnormal DNA methylation
|
J:236197
|
Dhhtm1Amc/Dhhtm1Amc
(involves: 129S1/Sv)
|
azoospermia
|
J:57914
|
decreased spermatid number
|
J:57914
|
Dhhtm1Amc/Dhhtm1Amc
(involves: 129S1/Sv * C57BL/6J)
|
azoospermia
|
J:57914
|
Dhhtm1Amc/Dhhtm1Amc
(involves: 129S1/Sv * C57BL/6J * Swiss Webster)
|
abnormal male germ cell morphology
|
J:65900
|
abnormal spermatocyte morphology
|
J:65900
|
decreased spermatogonia number
|
J:65900
|
DhpsGt(RRM039)Byg/DhpsGt(RRM039)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cell proliferation
|
J:285882
|
Dhtkd1tm1Mmgu/Dhtkd1tm1Mmgu
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased mitochondrial number
|
J:288186
|
increased mitochondrial size
|
J:288186
|
Dhx9tm1Ehl/Dhx9tm1Ehl
(involves: 129S1/Sv * C57BL/6)
|
increased ectoderm apoptosis
|
J:50931
|
increased embryonic tissue cell apoptosis
|
J:50931
|
Dhx9tm1Ehl/Dhx9tm1Ehl
(involves: 129S1/Sv * Black Swiss)
|
increased ectoderm apoptosis
|
J:50931
|
Dhx15tm1c(EUCOMM)Wtsi/Dhx15tm1c(EUCOMM)Wtsi Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C3H * C57BL/6N)
|
decreased B cell proliferation
|
J:284624
|
Dhx36tm1.2Pmt/Dhx36tm1.2Pmt Commd10Tg(Vav1-icre)A2Kio/Commd10+
(involves: 129P2/Ola * 129S4/SvJaeSor * C57BL/6 * C57BL/10 * CBA/Ca)
|
abnormal cell cycle
|
J:185179
|
Dhx58tm1Itl/Dhx58tm1Itl
(C57BL/6-Dhx58tm1Itl)
|
increased T cell apoptosis
|
J:187386
|
Diaph1tm1.1Sna/Diaph1tm1.1Sna
(B6.Cg-Diaph1tm1.1Sna)
|
abnormal leukocyte migration
|
J:126090
|
decreased T cell proliferation
|
J:126090
|
Diaph1tm1.1Sna/Diaph1tm1.1Sna Diaph2tm1.2Sna/Y
(B6N.Cg-Diaph1tm1.1Sna Diahp2tm1.2Sna)
|
abnormal neuronal migration
|
J:215740
|
Diaph1tm1.1Sna/Diaph1tm1.1Sna Diaph2tm1.2Sna/Diaph2tm1.2Sna
(B6N.Cg-Diaph1tm1.1Sna Diahp2tm1.2Sna)
|
abnormal neuronal migration
|
J:215740
|
Diaph3tm1.1Sna/Diaph3tm1.1Sna
(B6NSlc.Cg-Diaph3tm1.1Sna)
|
abnormal cell cycle
|
J:205519
|
Dicer1em1Psv/Dicer1em1Psv
(involves: C57BL/6NCrl)
|
abnormal female meiosis
|
J:203415
|
abnormal spindle assembly in female meiosis
|
J:203415
|
Dicer1em2Psv/Dicer1em2Psv
(involves: C57BL/6NCrl)
|
abnormal female meiosis
|
J:203415
|
abnormal spindle assembly in female meiosis
|
J:203415
|
Dicer1em3Psv/Dicer1em3Psv
(involves: C57BL/6NCrl)
|
abnormal female meiosis
|
J:203415
|
abnormal spindle assembly in female meiosis
|
J:203415
|
Dicer1tm1.1Mnn/Dicer1tm1.2Mnn Tg(Zp3-cre)93Knw/0
(involves: 129S1/SvImJ * C57BL/6J)
|
abnormal female meiosis
|
J:150221
|
abnormal oocyte morphology
|
J:150221
|
abnormal spindle assembly in female meiosis
|
J:150221
|
Dicer1tm1Bdh/Dicer1tm1Bdh Defb41tm1(icre)Psip/Defb41+
(involves: 129S6/SvEvTac * C57BL/6N)
|
oligozoospermia
|
J:187838
|
Dicer1tm1Bdh/Dicer1tm1Bdh Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal male germ cell morphology
|
J:145178
|
azoospermia
|
J:145178
|
decreased elongated spermatid number
|
J:145178
|
decreased male germ cell number
|
J:145178
|
decreased round spermatid number
|
J:145178
|
decreased spermatid number
|
J:145178
|
increased male germ cell apoptosis
|
J:145178
|
increased Sertoli cell proliferation
|
J:145178
|
Dicer1tm1Bdh/Dicer1tm1Bdh Tg(NEUROG3-cre)1Herr/0
(involves: 129 * C57BL/6J)
|
abnormal acrosome morphology
|
J:177677
|
abnormal Golgi apparatus morphology
|
J:177677
|
abnormal manchette morphology
|
J:177677
|
abnormal sperm flagellum morphology
|
J:177677
|
abnormal sperm head morphology
|
J:177677
|
abnormal sperm midpiece morphology
|
J:177677
|
abnormal sperm mitochondrial sheath morphology
|
J:177677
|
abnormal sperm nucleus morphology
|
J:177677
|
abnormal spermatid morphology
|
J:177677
|
absent sperm fibrous sheath
|
J:177677
|
absent sperm mitochondrial sheath
|
J:177677
|
decreased male germ cell number
|
J:177677
|
ectopic manchette
|
J:177677
|
increased male germ cell apoptosis
|
J:177677
|
kinked sperm flagellum
|
J:177677
|
oligozoospermia
|
J:177677
|
pinhead sperm
|
J:177677
|
small sperm head
|
J:177677
|
teratozoospermia
|
J:177677
|
thin sperm flagellum
|
J:177677
|
Dicer1tm1Bdh/Dicer1tm1Bdh Tg(Pax2-cre)1Akg/0
(involves: 129)
|
decreased cell proliferation
|
J:200017
|
Dicer1tm1Dli/Dicer1tm1Dli Tg(Cd4-cre)1Cwi/?
(involves: 129 * C57BL/6 * DBA/2)
|
abnormal cell physiology
|
J:100546
|
decreased T cell proliferation
|
J:100546
|
increased T cell apoptosis
|
J:100546
|
Dicer1tm1Mmk/Dicer1tm1Mmk Shhtm1(EGFP/cre)Cjt/Shh+
(involves: 129 * C57BL/6J)
|
increased mesenchymal cell proliferation involved in lung development
|
J:224791
|
Dicer1tm1Mmk/Dicer1tm1Mmk Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
(involves: 129 * C57BL/6 * CD-1)
|
abnormal granulocyte differentiation
|
J:158901
|
abnormal megakaryocyte differentiation
|
J:158901
|
Dicer1tm1Smr/Dicer1tm1Smr Pax8tm1.1(cre)Mbu/Pax8+
(involves: 129P2/OlaHsd * 129S7/SvEvBrd)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:229188
|
increased kidney apoptosis
|
J:229188
|
increased kidney cell proliferation
|
J:229188
|
Dicer1tm1Smr/Dicer1tm1Smr Tg(KRT5-rtTA)1Glk/0 Tg(tetO-cre)1Jaw/0
(involves: 129S7/SvEvBrd * C57BL/6 * FVB/N)
|
increased apoptosis
|
J:183487
|
Dicer1tm1Smr/Dicer1tm1Smr Tg(Myh6-cre)2182Mds/0
(involves: 129S7/SvEvBrd * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:131962
|
Dicer1tm1Snj/Dicer1tm1Snj
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:139257
|
abnormal mitosis
|
J:139257
|
decreased cell proliferation
|
J:139257
|
decreased DNA replication
|
J:139257
|
early cellular replicative senescence
|
J:139257
|
Dicer1tm1Snj/Dicer1tm1Snj Trp53tm1Brd/Trp53tm1Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased cell proliferation
|
J:139257
|
Dicer1tm1Snj/Dicer1tm1Snj Trp53tm1Brd/Trp53tm1Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
cellular phenotype
|
J:139257
|
Dicer1tm1Tara/Dicer1tm1Tara Tg(KRT14-cre)1Efu/?
(involves: 129P2/OlaHsd * CD-1)
|
increased apoptosis
|
J:106792
|
Dido1tm1Cmar/Dido1tm1Cmar
(involves: 129S1/Sv * 129X1/SvJ)
|
cellular phenotype
|
J:101201
|
Dido1tm1Cmar/Dido1tm2Cmar
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal centrosome morphology
|
J:183346
|
abnormal chromosome morphology
|
J:183346
|
abnormal mitosis
|
J:183346
|
aneuploidy
|
J:183346
|
Dido1tm2Cmar/Dido1tm2Cmar
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell differentiation
|
J:183346
|
abnormal centrosome morphology
|
J:183346
|
aneuploidy
|
J:183346
|
decreased embryonic epiblast cell proliferation
|
J:183346
|
increased embryonic epiblast cell apoptosis
|
J:183346
|
Dido1tm3Cmar/Dido1tm3.1Cmar Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
(involves: 129S/SvEv * C57BL/6)
|
increased hepatocyte karyomegaly
|
J:328215
|
Dinotm1.1Hyc/Dinotm1.1Hyc
(involves: C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:259337
|
Dinotm2.1Hyc/Dinotm2.1Hyc
(involves: C57BL/6)
|
decreased cellular sensitivity to DNA damaging agents
|
J:259337
|
delayed cellular replicative senescence
|
J:259337
|
Dio3tm1Dmst/Dio3tm1Dmst Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA)
|
increased hepatocyte proliferation
|
J:218350
|
Dio3tm1Stg/Dio3tm1Stg
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
maternal imprinting
|
J:80434
|
Dipk1cem1Yxy/Dipk1cem1Yxy
(C57BL/6-Dipk1cem1Yxy)
|
increased sensitivity to induced cell death
|
J:328853
|
Dis3l2em1Dean/Dis3l2em1Dean Tg(Zp3-cre)93Knw/0
(involves: C57BL/6 * C57BL/6J * DBA/2)
|
abnormal female meiosis
|
J:337555
|
abnormal oocyte morphology
|
J:337555
|
abnormal translation
|
J:337555
|
Disp1icb/Disp1tm2Amc Shhtm1(EGFP/cre)Cjt/Shh+
(involves: 129/Sv * C57BL/6J * SWR)
|
abnormal neuron differentiation
|
J:94270
|
Disp1tm2.1Amc/Disp1tm2.1Amc Shhtm1Amc/Shh+
(involves: 129/Sv * C57BL/6J * SWR)
|
abnormal neuron differentiation
|
J:94270
|
Disp1tm2.1Amc/Disp1tm2Amc Shhtm1(EGFP/cre)Cjt/Shh+
(involves: 129/Sv * C57BL/6J * SWR)
|
abnormal neuron differentiation
|
J:94270
|
Dkc1tm1.1Pjma/Y
(involves: 129X1/SvJ * C57BL/6 * FVB/N)
|
abnormal DNA repair
|
J:138335
|
Dkc1tm1.1Pjma/Y
(B6.129X1(FVB)-Dkc1tm1.1Pjma)
|
abnormal cell physiology
|
J:217050
|
decreased fibroblast proliferation
|
J:217050
|
decreased hematopoietic stem cell proliferation
|
J:217050
|
oxidative stress
|
J:217050
|
Dkc1tm1Bsl/Dkc1+ Tg(Gata1-cre)1Sho/0
(involves: 129/Sv * C57BL/6 * CD-1)
|
increased trophectoderm apoptosis
|
J:80494
|
Dkc1tm1Ppp/Y
(involves: 129S1/Sv)
|
abnormal cell physiology
|
J:81054
|
decreased telomere length
|
J:81054
|
increased fibroblast apoptosis
|
J:81054
|
Dkc1tm1Ppp/Dkc1+
(involves: 129S1/Sv)
|
abnormal cell morphology
|
J:81054
|
abnormal cell physiology
|
J:81054
|
Dkc1tm2Bsl/Dkc1+ Tg(Gata1-cre)1Sho/0
(involves: 129/Sv * C57BL/6 * CD-1)
|
increased trophectoderm apoptosis
|
J:80494
|
Dkc1tm2Pjma/Y
(chimera involves: 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:149894
|
Dkk1tm1.1Svo/Dkk1tm1.2Svo Pax8tm1.1(cre)Mbu/Pax8+
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
increased kidney cell proliferation
|
J:173125
|
Dkk2tm1Dwu/Dkk2tm1Dwu
(involves: 129)
|
abnormal osteoblast differentiation
|
J:100858
|
abnormal osteoclast differentiation
|
J:100858
|
Dkkl1tm1Ducy/Dkkl1tm1Ducy
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal male germ cell apoptosis
|
J:146994
|
Dlc1Gt(XE082)Byg/Dlc1Gt(XE082)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased fibroblast cell migration
|
J:189950
|
Dlc1tm1.1Lowy/Dlc1tm1.1Lowy
(involves: 129 * C57BL/6)
|
abnormal cell physiology
|
J:192878
|
Dlc1tm1Lec/Dlc1tm1Lec
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell adhesion
|
J:96194
|
Dlec1em1Yogo/Dlec1em1Yogo
(C57BL/6NSlc-Dlec1em1Yogo)
|
abnormal acrosome morphology
|
J:299542
|
abnormal manchette morphology
|
J:299542
|
abnormal sperm flagellum morphology
|
J:299542
|
abnormal sperm head morphology
|
J:299542
|
abnormal sperm mitochondrial sheath morphology
|
J:299542
|
abnormal sperm nucleus morphology
|
J:299542
|
asthenozoospermia
|
J:299542
|
oligozoospermia
|
J:299542
|
Dlg1tm1.1Agri/Dlg1tm1.1Agri Tg(Cryaa-cre)10Mlr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
increased lens epithelium apoptosis
|
J:151538
|
increased lens fiber apoptosis
|
J:151538
|
Dlg1tm1.1Agri/Dlg1tm1.1Agri Tg(Cryaa-cre,Tyr)39Mlr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
increased lens fiber apoptosis
|
J:151538
|
Dlg4tm1.1Tdoi/Dlg4tm1.1Tdoi
(B6.Cg-Dlg4tm1.1Tdoi)
|
maternal effect
|
J:197875
|
Dlg5tm1Vv/Dlg5tm1Vv
(involves: 129 * C57BL/6)
|
abnormal neuron differentiation
|
J:124940
|
Dlk1tm1.1Jvs/Dlk1+ Myf5tm3(cre)Sor/Myf5+
(involves: 129P2/SvPas * 129S4/SvJaeSor * C57BL/6 * FVB/N)
|
abnormal cell differentiation
|
J:167124
|
decreased cell proliferation
|
J:167124
|
maternal imprinting
|
J:167124
|
Dlk1tm1.2Jvs/Dlk1tm1.2Jvs
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
maternal imprinting
|
J:194130
|
Dlk1tm1Hsul/Dlk1+
(involves: 129 * C57BL/6J)
|
maternal imprinting
|
J:77909
|
Dlk1tm1Srba/Dlk1+
(involves: 129X1/SvJ * C57BL/6)
|
maternal imprinting
|
J:145076
|
Dll1tm1Gos/Dll1tm1Gos
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:156172
|
Dll1tm1Gos/Dll1tm1Gos
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuron differentiation
|
J:39633
|
absent embryonic cilia
|
J:80018
|
Dll1tm1Gos/Dll1tm2Gos
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal myoblast differentiation
|
J:119082
|
abnormal myotube differentiation
|
J:119082
|
Dll4tm1Grid/Dll4+
(either: (involves: 129X1/SvJ * Black Swiss) or (involves: 129X1/SvJ * C57BL/6J))
|
abnormal vascular regression
|
J:93125
|
Dll4tm1Jrt/Dll4tm1Jrt
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
abnormal vascular regression
|
J:93157
|
Dll4tm1Nwg/Dll4+
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac)
|
abnormal vascular regression
|
J:94740
|
Dll4tm2.1Vlcg/Dll4+ Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6NTac)
|
abnormal vascular regression
|
J:177797
|
Dlx5tm1Jlr/Dlx5tm1Jlr
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal axon extension
|
J:56559
|
Dlx5tm1Levi/Dlx5tm1Levi
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
abnormal cell proliferation
|
J:56557
|
abnormal osteoblast differentiation
|
J:56557
|
Dmap1tm1.2Jrc/Dmap1+ Dnmt1tm2Jrc/Dnmt1tm2Jrc
(involves: 129S1/Sv * C57BL/6 * FVB/N * SJL)
|
abnormal DNA methylation
|
J:172814
|
Dmbt1tm1Qaa/Dmbt1tm1Qaa
(either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * SWR))
|
abnormal inner cell mass apoptosis
|
J:93477
|
Dmc1Mei11/Dmc1+
(involves: 129S4/SvJae * C3HeB/FeJ * C57BL/6J)
|
abnormal female meiosis
|
J:122037
|
abnormal spermatocyte morphology
|
J:122037
|
arrest of male meiosis
|
J:122037
|
decreased oocyte number
|
J:122037
|
Dmc1Mei11/Dmc1+
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal female meiosis
|
J:122037
|
arrest of male meiosis
|
J:122037
|
Dmc1Mei11/Dmc1Mei11
(involves: 129S4/SvJae * C57BL/6J)
|
decreased male germ cell number
|
J:60747
|
Dmc1tm1Jcs/Dmc1Mei11
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal spermatocyte morphology
|
J:122037
|
arrest of male meiosis
|
J:122037
|
decreased oocyte number
|
J:122037
|
Dmc1tm1Jcs/Dmc1tm1Jcs
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal female meiosis
|
J:47308
|
abnormal oogenesis
|
J:47308
|
absent oocytes
|
J:47308,
J:183982
|
arrest of male meiosis
|
J:47308
|
azoospermia
|
J:47308
|
Dmc1tm1Jcs/Dmc1tm1Jcs
(involves: 129S4/SvJae * C57BL/6)
|
abnormal male meiosis
|
J:194067
|
Dmc1tm1Jcs/Dmc1tm1Jcs Hormad1tm1.2Atot/Hormad1tm1.2Atot
(involves: 129/Sv * BALB/c * C57BL/6 * SJL)
|
abnormal double-strand DNA break repair
|
J:173089
|
Dmc1tm1Jcs/Dmc1tm1Jcs Hormad1tm1Atot/Hormad1tm1Atot
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:173089
|
Dmc1tm1Jcs/Dmc1tm1Jcs Hormad2tm1.2Atot/Hormad2tm1.2Atot
(involves: 129 * BALB/c * C57BL/6 * SJL)
|
absent oocytes
|
J:183982
|
Dmc1tm1Tkm/Dmc1tm1Tkm
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal oogenesis
|
J:47307
|
absent oocytes
|
J:47307
|
arrest of male meiosis
|
J:47307
|
azoospermia
|
J:47307
|
Dmdmdx-4Cv/Dmdmdx-4Cv Terctm1Rdp/Terctm1Rdp
(B6.Cg-Terctm1Rdp Dmdmdx-4Cv)
|
abnormal mitochondrial shape
|
J:200365
|
decreased mitochondrial size
|
J:200365
|
decreased telomere length
|
J:200365
|
disorganized mitochondrial cristae
|
J:200365
|
increased mitochondrial number
|
J:200365
|
oxidative stress
|
J:200365
|
Dmdmdx/? Myod1tm1Jae/Myod1tm1Jae
(involves: 129S4/SvJae * C57BL/10ScSn)
|
cardiac interstitial fibrosis
|
J:52248
|
Dmdmdx/Y Terctm1Rdp/Terctm1Rdp
(involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL)
|
chromosomal instability
|
J:167294
|
decreased telomere length
|
J:167294
|
Dmdmdx/Dmdmdx
(involves: C57BL/10ScSn)
|
abnormal skeletal muscle satellite cell proliferation
|
J:152892
|
Dmdmdx/Dmdmdx Mamstrtm1.2Eno/Mamstrtm1.2Eno
(involves: 129 * C57BL/6 * C57BL/10ScSn)
|
abnormal skeletal muscle satellite cell proliferation
|
J:179880
|
Dmdtm1Mok/Y
(involves: 129S/SvEv)
|
abnormal plasma membrane morphology
|
J:102549
|
Dmdtm1Mok/Dmdtm1Mok
(involves: 129S/SvEv)
|
abnormal plasma membrane morphology
|
J:102549
|
Dmp1tm1Mis/Dmp1tm1Mis
(involves: 129S7/SvEvBrd * CD-1)
|
arrested osteoblast differentiation
|
J:184352
|
Dmrt1tm1.1Zark/Dmrt1tm1.1Zark
(involves: 129 * C57BL/6)
|
abnormal male meiosis
|
J:65541
|
decreased male germ cell number
|
J:65541
|
increased Sertoli cell proliferation
|
J:65541
|
Dmrt1tm1Zark/Dmrt1tm1.1Zark Tg(Dhh-cre)1Mejr/0
(involves: 129/Sv * C57BL/6)
|
abnormal spermatogonia morphology
|
J:122954
|
Dmrta2tm1.2Fuma/Dmrta2tm1.2Fuma
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * FVB/N * SJL)
|
abnormal neuronal precursor proliferation
|
J:203109
|
Dmrta2tm1Ejbd/Dmrta2tm1Ejbd
(involves: C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:215514
|
Dmrtb1tm1.1Zark/Dmrtb1tm1.1Zark
(involves: 129S1/Sv * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:217504
|
Dmrtb1tm1.1Zark/Dmrtb1tm1.1Zark
(involves: 129S1/Sv)
|
abnormal male meiosis
|
J:217504
|
abnormal synaptonemal complex
|
J:217504
|
arrest of male meiosis
|
J:217504
|
Dmrtc2tm1(cre)Knis/Dmrtc2tm1(cre)Knis
(involves: 129P2/OlaHsd * C57BL/6J)
|
arrest of male meiosis
|
J:117721
|
azoospermia
|
J:117721
|
decreased spermatid number
|
J:117721
|
Dmrtc2tm1.2Zark/Dmrtc2tm1.2Zark
(involves: 129S1/Sv * C57BL/6)
|
abnormal male germ cell morphology
|
J:121537
|
abnormal spermatocyte morphology
|
J:121537
|
abnormal spermatogonia morphology
|
J:121537
|
arrest of male meiosis
|
J:121537
|
decreased male germ cell number
|
J:121537
|
decreased spermatid number
|
J:121537
|
increased male germ cell apoptosis
|
J:121537
|
Dms/Dms+
(involves: C57BL/6 * DBA/2)
|
arrest of male meiosis
|
J:75005
|
azoospermia
|
J:75005
|
Dna2tm1.1Lzhg/Dna2+
(involves: 129S1/Sv)
|
abnormal chromosome morphology
|
J:198831
|
abnormal mitosis
|
J:198831
|
abnormal telomere morphology
|
J:198831
|
aneuploidy
|
J:198831
|
chromosomal instability
|
J:198831
|
decreased telomere length
|
J:198831
|
Dnaaf2tm1.1(KOMP)Vlcg/Dnaaf2tm1.1(KOMP)Vlcg
(B6N(Cg)-Dnaaf2tm1.1(KOMP)Vlcg/J)
|
decreased embryonic cilium number
|
J:278736
|
increased embryonic tissue cell apoptosis
|
J:278736
|
increased neural tube apoptosis
|
J:278736
|
increased tail bud apoptosis
|
J:278736
|
Dnaaf2tm1.1Mkis/Dnaaf2tm1.1Mkis
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal brain ependyma motile cilium location or orientation
|
J:201474
|
abnormal brain ependyma motile cilium morphology
|
J:201474
|
abnormal brain ependyma motile cilium physiology
|
J:201474
|
immotile respiratory cilia
|
J:201474
|
Dnaaf3b2b1739Clo/Dnaaf3b2b1739Clo
(C57BL/6J-Dnaaf3b2b1739Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnaaf4b2b811.1Clo/Dnaaf4b2b811.1Clo
(C57BL/6J-Dnaaf4b2b811.1Clo)
|
abnormal brain ependyma motile cilium physiology
|
J:205312
|
immotile respiratory cilia
|
J:175213
|
Dnaaf4tm1.2Jjlo/Dnaaf4tm1.2Jjlo
(involves: 129S1/Sv * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J)
|
abnormal brain ependyma motile cilium physiology
|
J:205312
|
abnormal respiratory motile cilium physiology
|
J:205312
|
Dnaaf5em1Slb/Dnaaf5em1Slb
(C57BL/6-Dnaaf5em1Slb)
|
abnormal brain ependyma motile cilium morphology
|
J:342770
|
abnormal brain ependyma motile cilium physiology
|
J:342770
|
abnormal respiratory motile cilium morphology
|
J:342770
|
abnormal respiratory motile cilium physiology
|
J:342770
|
cellular phenotype
|
J:342770
|
immotile respiratory cilia
|
J:342770
|
immotile sperm
|
J:342770
|
Dnaaf5em1Slb/Dnaaf5em2Slb
(C57BL/6-Dnaaf5em1Slb Dnaaf5em2Slb)
|
abnormal brain ependyma motile cilium morphology
|
J:342770
|
abnormal respiratory motile cilium morphology
|
J:342770
|
immotile respiratory cilia
|
J:342770
|
Dnaaf6rttm1.2Hmd/Dnaaf6rttm1.2Hmd
(involves: ICR)
|
abnormal sperm axoneme morphology
|
J:208266
|
abnormal sperm flagellum morphology
|
J:208266
|
asthenozoospermia
|
J:208266
|
short sperm flagellum
|
J:208266
|
thin sperm flagellum
|
J:208266
|
Dnaaf11tm1.1Hmd/Dnaaf11tm1.1Hmd Nanos3tm2.1(cre)Ysa/Nanos3+
(involves: 129S6/SvEvTac * C57BL/6NCrlj * CBA/JNCrlj)
|
immotile sperm
|
J:258369
|
Dnaaf11tm1.2Hmd/Dnaaf11tm1.2Hmd
(involves: 129S6/SvEvTac * C57BL/6NCrl)
|
abnormal brain ependyma motile cilium physiology
|
J:258369
|
abnormal motile primary cilium physiology
|
J:258369
|
abnormal respiratory motile cilium morphology
|
J:258369
|
immotile respiratory cilia
|
J:258369
|
Dnah1ferf1/Dnah1ferf1
(C3Fe.B6-Dnah1ferf1)
|
asthenozoospermia
|
J:308831
|
decreased sperm progressive motility
|
J:308831
|
Dnah1tm1Ihgg/Dnah1tm1Ihgg
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
asthenozoospermia
|
J:69800
|
Dnah2em1(IMPC)Tcp/Dnah2em1(IMPC)Tcp
(involves: C57BL/6NCrl)
|
abnormal outer dense fiber morphology
|
J:307872
|
abnormal sperm annulus morphology
|
J:307872
|
abnormal sperm axoneme morphology
|
J:307872
|
abnormal sperm connecting piece morphology
|
J:307872
|
abnormal sperm end piece morphology
|
J:307872
|
abnormal sperm fibrous sheath morphology
|
J:307872
|
abnormal sperm flagellum morphology
|
J:307872
|
abnormal sperm flagellum thickness
|
J:307872
|
abnormal sperm head morphology
|
J:307872
|
abnormal sperm midpiece morphology
|
J:307872
|
abnormal sperm mitochondrial sheath morphology
|
J:307872
|
abnormal sperm principal piece morphology
|
J:307872
|
absent sperm fibrous sheath
|
J:307872
|
absent sperm flagellum
|
J:307872
|
absent sperm mitochondrial sheath
|
J:307872
|
cellular phenotype
|
J:307872
|
coiled sperm flagellum
|
J:307872
|
immotile sperm
|
J:307872
|
kinked sperm flagellum
|
J:307872
|
oligozoospermia
|
J:307872
|
short sperm flagellum
|
J:307872
|
Dnah5b2b016Clo/Dnah5b2b016Clo
(C57BL/6J-Dnah5b2b016Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
Dnah5b2b601Clo/Dnah5b2b601Clo
(C57BL/6J-Dnah5b2b601Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah5b2b1003Clo/Dnah5b2b1003Clo
(C57BL/6J-Dnah5b2b1003Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah5b2b1134Clo/Dnah5b2b1134Clo
(C57BL/6J-Dnah5b2b1134Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah5b2b1154Clo/Dnah5b2b1154Clo
(C57BL/6J-Dnah5b2b1154Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah5b2b1537Clo/Dnah5b2b1537Clo
(C57BL/6J-Dnah5b2b1537Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah5b2b1565Clo/Dnah5b2b1565Clo
(C57BL/6J-Dnah5b2b1565Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah5b2b2395Clo/Dnah5b2b2395Clo
(C57BL/6J-Dnah5b2b2395Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah5hlb612/Dnah5+
(involves: C57BL/6J)
|
abnormal respiratory motile cilium morphology
|
J:130755
|
Dnah5hlb612/Dnah5hlb612
(involves: C57BL/6J)
|
abnormal respiratory motile cilium morphology
|
J:130755
|
abnormal respiratory motile cilium physiology
|
J:130755
|
Dnah5Tg1Htz/Dnah5Tg1Htz
(involves: C57BL/6 * CBA/J)
|
immotile respiratory cilia
|
J:76189
|
Dnah8em1Osb/Dnah8em1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal outer dense fiber morphology
|
J:297137
|
abnormal sperm axoneme morphology
|
J:297137
|
abnormal sperm fibrous sheath morphology
|
J:297137
|
abnormal sperm flagellum morphology
|
J:297137
|
absent sperm flagellum
|
J:297137
|
coiled sperm flagellum
|
J:297137
|
disorganized sperm mitochondrial sheath
|
J:297137
|
immotile sperm
|
J:297137
|
kinked sperm flagellum
|
J:297137
|
short sperm flagellum
|
J:297137
|
Dnah9em1Hmd/Dnah9em1Hmd
(C57BL/6-Dnah9em1Hmd)
|
abnormal ependyma motile cilium morphology
|
J:301033
|
abnormal respiratory motile cilium morphology
|
J:301033
|
Dnah10em1Yxc/Dnah10em1Yxc
(involves: C57BL/6)
|
abnormal sperm flagellum morphology
|
J:311550
|
absent sperm flagellum
|
J:311550
|
coiled sperm flagellum
|
J:311550
|
disorganized sperm mitochondrial sheath
|
J:311550
|
immotile sperm
|
J:311550
|
oligozoospermia
|
J:311550
|
short sperm flagellum
|
J:311550
|
Dnah10em2Yxc/Dnah10em2Yxc
(involves: C57BL/6)
|
abnormal sperm flagellum morphology
|
J:311550
|
absent sperm flagellum
|
J:311550
|
coiled sperm flagellum
|
J:311550
|
disorganized sperm mitochondrial sheath
|
J:311550
|
immotile sperm
|
J:311550
|
oligozoospermia
|
J:311550
|
short sperm flagellum
|
J:311550
|
Dnah11b2b598Clo/Dnah11b2b598Clo
(C57BL/6J-Dnah11b2b598Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
Dnah11b2b1203Clo/Dnah11b2b1203Clo
(C57BL/6J-Dnah11b2b1203Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah11b2b1279Clo/Dnah11b2b1279Clo
(C57BL/6J-Dnah11b2b1279Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
Dnah11b2b1468.2Clo/Dnah11b2b1468.2Clo
(C57BL/6J-Dnah11b2b1468.2Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnah11b2b1727Clo/Dnah11b2b1727Clo
(C57BL/6J-Dnah11b2b1727Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
immotile respiratory cilia
|
J:175213
|
Dnah11b2b1775Clo/Dnah11b2b1775Clo
(C57BL/6J-Dnah11b2b1775Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
Dnah11iv/Dnah11iv
(involves: C3H)
|
abnormal motile primary cilium morphology
|
J:109561
|
absent nodal flow
|
J:109561
|
Dnah11tm1Bknr/Dnah11tm1Bknr
(involves: 129S1/Sv)
|
abnormal motile primary cilium physiology
|
J:107740
|
Dnah11tm1Ssp/Dnah11tm1Ssp
(Not Specified)
|
abnormal motile primary cilium physiology
|
J:44522
|
absent nodal flow
|
J:44522
|
Dnah17em1Qsh/Dnah17em1Qsh
(involves: C57BL/6 * DBA/2J)
|
abnormal sperm axoneme morphology
|
J:285088
|
asthenozoospermia
|
J:285088
|
globozoospermia
|
J:285088
|
oligozoospermia
|
J:285088
|
Dnah17em2Qsh/Dnah17em2Qsh
(involves: C57BL/6 * DBA/2J)
|
abnormal sperm axoneme morphology
|
J:285088
|
Dnai1b2b284Clo/Dnai1b2b284Clo
(C57BL/6J-Dnai1b2b284Clo)
|
abnormal motile cilium morphology
|
J:216862
|
abnormal motile cilium physiology
|
J:216862
|
abnormal respiratory motile cilium morphology
|
J:216862
|
Dnai1b2b1526Clo/Dnai1b2b1526Clo
(C57BL/6J-Dnai1b2b1526Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnai2b2b3405Clo/Dnai2b2b3405Clo
(C57BL/6J-Dnai2b2b3405Clo)
|
immotile respiratory cilia
|
J:175213
|
Dnaja1tm1Kate/Dnaja1tm1Kate
(involves: C57BL/6 * CBA)
|
abnormal spermatocyte morphology
|
J:96238
|
asthenozoospermia
|
J:96238
|
decreased elongated spermatid number
|
J:96238
|
oligozoospermia
|
J:96238
|
Dnaja3tm1.1Jdl/Dnaja3tm1.1Jdl Tg(Myhca-cre)1Abel/0
(involves: 129X1/SvJ * C57BL/6J * FVB)
|
abnormal respiratory electron transport chain
|
J:104462
|
cardiac interstitial fibrosis
|
J:104462
|
decreased myocardial fiber mitochondrial DNA content
|
J:104462
|
dilated mitochondrion
|
J:104462
|
increased cardiomyocyte apoptosis
|
J:104462
|
Dnajb9Gt(KST256)Byg/Dnajb9Gt(KST256)Byg
(129P2/OlaHsd-Dnajb9Gt(KST256)Byg)
|
abnormal endoplasmic reticulum morphology
|
J:226674
|
increased cell death
|
J:226674
|
Dnajb9Gt(KST256)Byg/Dnajb9Gt(KST256)Byg
(B6.129P2-Dnajb9Gt(KST256)Byg)
|
abnormal endoplasmic reticulum morphology
|
J:226674
|
increased cell death
|
J:226674
|
Dnajb9Gt(KST256)Byg/Dnajb9Gt(KST256)Byg Tg(CAG-XBP1*/Venus)#Miur/?
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal endoplasmic reticulum morphology
|
J:226674
|
increased pancreatic beta cell apoptosis
|
J:226674
|
Dnajc10tm1Tiw/Dnajc10tm1Tiw Gt(ROSA)26Sortm1.2Tiw/Gt(ROSA)26Sor+
(involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6)
|
increased endoplasmic reticulum stress
|
J:159968
|
Dnajc11spc/Dnajc11spc
(B6.Cg-Dnajc11spc)
|
disorganized mitochondrial cristae
|
J:221543
|
Dnajc15Gt(RRN226)Byg/Dnajc15Gt(RRN226)Byg
(B6.129P2-Dnajc15Gt(RRN226)Byg)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:204025
|
Dnajc27Gt(OST374030)Lex/Dnajc27Gt(OST374030)Lex
(involves: 129S5/SvEvBrd * C57BL/6N)
|
abnormal enterocyte proliferation
|
J:210622
|
Dnajc30tm1(KOMP)Vlcg/Dnajc30tm1(KOMP)Vlcg Tg(Thy1-YFP)HJrs/0
(involves: C57BL/6J * C57BL/6N)
|
abnormal mitochondrial morphology
|
J:266469
|
abnormal mitochondrial physiology
|
J:266469
|
abnormal mitochondrial shape
|
J:266469
|
increased mitochondrial fission
|
J:266469
|
increased mitochondrial number
|
J:266469
|
Dnali1em1Yxc/Dnali1em1Yxc
(C57BL/6-Dnali1em1Yxc)
|
abnormal sperm fibrous sheath morphology
|
J:340653
|
asthenozoospermia
|
J:340653
|
Dnase1tm1Tmo/Dnase1tm1Tmo
(involves: 129P2/OlaHsd * CD-1)
|
decreased kidney apoptosis
|
J:110060
|
Dnase1l2tm1Eckh/Dnase1l2tm1Eckh
(involves: 129S6/SvEvTac)
|
abnormal cell nucleus morphology
|
J:180935
|
Dnase1l3tm1Dkit/Dnase1l3tm1Dkit
(involves: C57BL/6)
|
abnormal cell death
|
J:211019
|
Dnase2atm1Aea/Dnase2atm1Aea
(involves: 129 * C57BL/6)
|
abnormal apoptosis
|
J:89469
|
Dnd1Ter/Dnd1+
(involves: 129S1/Sv * C57BL/6)
|
decreased germ cell number
|
J:7954
|
Dnd1Ter/Dnd1Ter
(129S1/Sv-KitW Oca2p Tyrc-ch)
|
decreased male germ cell number
|
J:7954
|
decreased oocyte number
|
J:7954
|
Dnd1tm1Na/Dnd1Ter
(involves: 129P3/J * 129S6/SvEvTac)
|
decreased male germ cell number
|
J:221231
|
Dnhd1em1Glin/Dnhd1em1Glin
(C57BL/6-Dnhd1em1Glin)
|
abnormal sperm flagellum morphology
|
J:321189
|
asthenozoospermia
|
J:321189
|
coiled sperm flagellum
|
J:321189
|
decreased sperm progressive motility
|
J:321189
|
hairpin sperm flagellum
|
J:321189
|
oligozoospermia
|
J:321189
|
short sperm flagellum
|
J:321189
|
Dnm1tm1Pdc/Dnm1tm1Pdc Dnm2tm1.1Pdc/Dnm2tm1.1Pdc
(involves: 129S1/SvImJ * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:161127
|
Dnm1lem1Hise/Dnm1lem1Hise
(involves: C57BL/6J * SJL/J)
|
cellular phenotype
|
J:291773
|
Dnm1lem1Hise/Dnm1lem1Hise Tg(Thy1-EGFP)MJrs/0
(involves: C57BL/6J * CBA * SJL/J)
|
cellular phenotype
|
J:291773
|
Dnm1lPy/Dnm1l+
(involves: BALB/cAnNCrl * C3H/HeH)
|
abnormal cellular respiration
|
J:161510
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:161510
|
abnormal mitochondrial morphology
|
J:161510
|
abnormal myocardial fiber mitochondrial morphology
|
J:161510
|
abnormal peroxisome morphology
|
J:161510
|
cardiac interstitial fibrosis
|
J:161510
|
Dnm1lPy/Dnm1lPy
(involves: BALB/cAnNCrl * C3H/HeH)
|
abnormal cell adhesion
|
J:161510
|
abnormal cell physiology
|
J:161510
|
abnormal mitochondrial morphology
|
J:161510
|
absent fibroblast proliferation
|
J:161510
|
Dnm1ltm1.1Hise/Dnm1ltm1.1Hise En1tm2(cre)Wrst/En1+
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal Purkinje cell mitochondrial morphology
|
J:153835
|
Dnm1ltm1.1Hise/Dnm1ltm1.2Hise En1tm2(cre)Wrst/En1+
(involves: 129 * C57BL/6 * FVB/N * SJL)
|
abnormal Purkinje cell mitochondrial morphology
|
J:153835
|
Dnm1ltm1.1Miha/Dnm1ltm1.1Miha Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal mitochondrial morphology
|
J:158142
|
increased neuron apoptosis
|
J:158142
|
Dnm1ltm1.2Hise/Dnm1ltm1.2Hise
(involves: 129S/SvEv * C57BL/6 * FVB/N)
|
abnormal mitochondrial morphology
|
J:153835
|
decreased apoptosis
|
J:153835
|
decreased fibroblast proliferation
|
J:153835
|
Dnm1ltm1.2Miha/Dnm1ltm1.2Miha
(involves: C57BL/6J)
|
abnormal mitochondrial morphology
|
J:158142
|
abnormal peroxisome morphology
|
J:158142
|
decreased fibroblast proliferation
|
J:158142
|
increased brain apoptosis
|
J:158142
|
increased mitochondrial size
|
J:158142
|
Dnm2tm1.1Ics/Dnm2tm1.1Ics
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell physiology
|
J:166364
|
Dnm2tm4.1Ics/Dnm2+
(involves: C57BL/6N)
|
abnormal mitochondrial crista morphology
|
J:329580
|
abnormal mitochondrial shape
|
J:329580
|
increased mitochondrial size
|
J:329580
|
Dnmt1em2Jiemw/Dnmt1+
(C57BL/6-Dnmt1em2Jiemw)
|
increased neuron apoptosis
|
J:310870
|
Dnmt1tm1Enl/Dnmt1tm1Enl
(involves: 129S4/SvJae)
|
abnormal DNA methylation
|
J:36234
|
Dnmt1tm1Enl/Dnmt1tm1Enl
(involves: 129S4/SvJae * C57BL/6)
|
abnormal DNA methylation
|
J:116773
|
Dnmt1tm1Enl/Dnmt1tm1Enl H19tm1Tilg/H19+
(involves: 129S/SvEv * 129S4/SvJae)
|
genetic imprinting
|
J:110857
|
Dnmt1tm1Jae/Dnmt1tm1Jae
(involves: 129S4/SvJae)
|
abnormal DNA methylation
|
J:1157
|
abnormal imprinting
|
J:110857
|
decreased cell proliferation
|
J:1157
|
increased embryonic tissue cell apoptosis
|
J:1157
|
Dnmt1tm1Jrc/Dnmt1tm1Jrc
(involves: 129S1/Sv * FVB/N)
|
abnormal imprinting
|
J:135338
|
Dnmt1tm1Jrc/Dnmt1tm1Jrc
(involves: 129S1/Sv)
|
abnormal imprinting
|
J:68455
|
Dnmt1tm1Okan/Dnmt1tm2Enl
(involves: 129S4/SvJae)
|
decreased cell proliferation
|
J:129049
|
Dnmt1tm2Enl/Dnmt1tm2Enl
(involves: 129S4/SvJae)
|
abnormal DNA methylation
|
J:36234
|
decreased cell proliferation
|
J:129049
|
Dnmt3aem1Hsas/Dnmt3a+
(C57BL/6J-Dnmt3aem1Hsas)
|
abnormal imprinting
|
J:349016
|
Dnmt3aem1Hsas/Dnmt3aem1Hsas
(C57BL/6J-Dnmt3aem1Hsas)
|
abnormal DNA methylation during gametogenesis
|
J:347433,
J:349016
|
abnormal imprinting
|
J:347433,
J:349016
|
Dnmt3aem1Hsas/Dnmt3aem1Hsas Dnmt3lem1Hsas/Dnmt3lem1Hsas
(C57BL/6J-Dnmt3aem1Hsas Dnmt3lem1Hsas)
|
abnormal DNA methylation during gametogenesis
|
J:347433
|
abnormal imprinting
|
J:347433
|
decreased spermatid number
|
J:347433
|
teratozoospermia
|
J:347433
|
Dnmt3atm1Jae/Dnmt3atm1Jae Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Nkx2-2tm2.1Suss/Nkx2-2tm2.1Suss Tg(Ins2-cre)23Herr/0
(involves: 129S/Sv * Black Swiss * C57BL/6 * CBA/J * SJL)
|
abnormal pancreatic beta cell differentiation
|
J:177838
|
Dnmt3atm2Enl/Dnmt3atm2Enl Dnmt3btm1Enl/Dnmt3btm1Enl
(involves: 129S4/SvJae * C57BL/6)
|
abnormal DNA methylation
|
J:116773
|
Dnmt3bMommeD14/Dnmt3bMommeD14 Tg(HBA1-GFP)1Ew/0
(involves: FVB/N)
|
abnormal epigenetic regulation of gene expression
|
J:198944
|
Dnmt3bMommeD14/Dnmt3btm1Enl Tg(HBA1-GFP)1Ew/0
(involves: FVB/N)
|
abnormal epigenetic regulation of gene expression
|
J:198944
|
Dnmt3btm1.1Ics/Dnmt3btm2.1Ics
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal DNA methylation
|
J:160567
|
Dnmt3btm1Enl/Dnmt3btm6Enl
(involves: 129S4/SvJae * C57BL/6)
|
increased thymocyte apoptosis
|
J:106540
|
Dnmt3btm1Enl/Dnmt3btm7Enl
(involves: 129S4/SvJae * C57BL/6)
|
increased thymocyte apoptosis
|
J:106540
|
Dnmt3btm6Enl/Dnmt3btm6Enl
(involves: 129S4/SvJae * C57BL/6)
|
increased thymocyte apoptosis
|
J:106540
|
Dnmt3btm6Enl/Dnmt3btm7Enl
(involves: 129S4/SvJae * C57BL/6)
|
increased thymocyte apoptosis
|
J:106540
|
Dnmt3btm7Enl/Dnmt3btm7Enl
(involves: 129S4/SvJae * C57BL/6)
|
increased thymocyte apoptosis
|
J:106540
|
Dnmt3cem2Sky/Dnmt3cem3Sky
(involves: C57BL/6 * CBA)
|
azoospermia
|
J:244795
|
Dnmt3cem4Sky/Dnmt3crahu
(involves: C57BL/6J * CBA * FVB/NJ)
|
azoospermia
|
J:244795
|
Dnmt3crahu/Dnmt3crahu
(involves: C57BL/6J * FVB/NJ)
|
abnormal DNA methylation during gametogenesis
|
J:244795
|
abnormal spermatocyte morphology
|
J:244795
|
arrest of male meiosis
|
J:244795
|
azoospermia
|
J:244795
|
increased male germ cell apoptosis
|
J:244795
|
Dnmt3lem1Hsas/Dnmt3lem1Hsas
(C57BL/6J-Dnmt3lem1Hsas)
|
abnormal DNA methylation during gametogenesis
|
J:347433
|
abnormal imprinting
|
J:347433
|
Dnmt3ltm1Bes/Dnmt3ltm1Bes
(involves: 129S6/SvEvTac)
|
abnormal oogenesis
|
J:73452
|
azoospermia
|
J:73452
|
decreased male germ cell number
|
J:128710
|
Dnmt3ltm1Enl/Dnmt3ltm1Enl
(involves: 129S4/SvJae)
|
abnormal oogenesis
|
J:75938
|
Dnmt3ltm1Scot/Dnmt3ltm1Scot
(C57BL/6-Dnmt3ltm1Scot)
|
arrest of male meiosis
|
J:97190
|
azoospermia
|
J:97190
|
Dnttip1em1Shmc/Dnttip1em1Shmc
(C57BL/6J-Dnttip1em1Shmc)
|
abnormal mitosis
|
J:291786
|
Dock1tm1.1Ysfk/Dock1tm1.1Ysfk
(B6(Cg)-Dock1tm1.1Ysfk)
|
abnormal vascular endothelial cell migration
|
J:178190
|
Dock1tm2.1Jfco/Dock1tm2.1Jfco Tg(MMTV-Erbb2*,-cre)1Mul/0
(involves: C57BL/6 * FVB/NJ)
|
decreased cell proliferation
|
J:196659
|
increased apoptosis
|
J:196659
|
Dock2m1Hsd/Dock2m1Hsd Siaetm1.2Avrk/Siaetm1.2Avrk
(B6NHsd.Cg-Siaetm1.2Avrk Dock2m1Hsd)
|
increased B cell proliferation
|
J:144035
|
Dock2tm1Tsas/Dock2tm1Tsas
(involves: C57BL/6)
|
abnormal leukocyte migration
|
J:71005
|
Dock2tm1Tsas/Dock2tm1Tsas
(B6.Cg-Dock2tm1Tsas)
|
abnormal cell migration
|
J:130919
|
impaired neutrophil chemotaxis
|
J:113266
|
Dock8pri/Dock8pri
(involves: C57BL/6JAnu)
|
abnormal cellular extravasation
|
J:238772
|
Dock8tm1Ysfk/Dock8tm1Ysfk
(B6.Cg-Dock8tm1Ysfk)
|
decreased T cell proliferation
|
J:185165
|
Dock10tm1Thar/Dock10tm1Thar
(involves: C57BL/6)
|
abnormal microglial cell chemotaxis
|
J:300632
|
impaired macrophage chemotaxis
|
J:300632
|
Dock11tm1Thar/Dock11tm1Thar
(involves: C57BL/6)
|
impaired macrophage chemotaxis
|
J:300632
|
Dok1tm1Ppp/Dok1tm1Ppp
(129S1/Sv-Dok1tm1Ppp)
|
abnormal T cell proliferation
|
J:95640
|
increased fibroblast proliferation
|
J:95640
|
Dok1tm1Yyam/Dok1tm1Yyam
(involves: 129S4/SvJae * C57BL/6)
|
increased B cell proliferation
|
J:95641
|
Dok3tm1Kplm/Dok3tm1Kplm
(involves: 129P2/OlaHsd)
|
increased B cell proliferation
|
J:280795
|
Donsonem1Anpj/Donsonem1Anpj
(involves: C57BL/6 * CBA * CD-1)
|
abnormal DNA replication
|
J:343338
|
Dot1ltm1.1Tche/Dot1ltm1.1Tche
(either: (involves: C57BL/6) or (involves: 129/Sv * C57BL/6))
|
abnormal cell physiology
|
J:161427
|
aneuploidy
|
J:161427
|
decreased cell proliferation
|
J:161427
|
increased embryonic tissue cell apoptosis
|
J:161427
|
increased telomere length
|
J:161427
|
Dot1ltm1Tche/Dot1ltm1.1Tche Tg(Myhca-cre)1Abel/0
(Not Specified)
|
cardiac interstitial fibrosis
|
J:168140
|
increased cardiomyocyte apoptosis
|
J:168140
|
increased fetal cardiomyocyte proliferation
|
J:168140
|
Dp(4D4Mit190-D4Mit51)1Aam/0
(involves: 129S7/SvEvBrd)
|
abnormal mitosis
|
J:121726
|
decreased cell proliferation
|
J:121726
|
early cellular replicative senescence
|
J:121726
|
increased neural tube apoptosis
|
J:121726
|
Dp(7Herc2-Mkrn3)1Taku/0
(involves: 129S7/SvEvBrd * C57BL/6)
|
genetic imprinting
|
J:151648
|
Dp(16Cbr1-Fam3b)1Rhr/0
(B6.129S6-Dp(16Cbr1-Fam3b)1Rhr)
|
abnormal brain ependyma motile cilium physiology
|
J:241597
|
Dp(16Cbr1-Fam3b)1Rhr/0 Pcp4tm1.1Kzy/Pcp4+
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N)
|
abnormal brain ependyma motile cilium physiology
|
J:241597
|
Dp(16Hspa13-App)2Yah/0
(B6J.129P2-Dp(16Hspa13-App)2Yah)
|
abnormal cellular respiration
|
J:223518
|
abnormal mitochondrial physiology
|
J:223518
|
decreased muscle fiber mitochondrial DNA content
|
J:223518
|
Dpcd/PollGt(OST280355)Lex/Dpcd/PollGt(OST280355)Lex
(involves: 129S5/SvEvBrd * C57BL/6Brd)
|
asthenozoospermia
|
J:171184,
J:185566
|
globozoospermia
|
J:171184,
J:185566
|
short sperm flagellum
|
J:171184,
J:185566
|
teratozoospermia
|
J:171184
|
Dpep3em1Qsh/Dpep3em1Qsh
(Not Specified)
|
oligozoospermia
|
J:289328
|
Dph1tm1Bhr/Dph1tm1Bhr
(either: 129/Sv or (involves: 129/Sv * C57BL/6))
|
abnormal cell cycle
|
J:88090
|
Dph1tm1Bhr/Dph1tm1Bhr
(involves: 129S4/SvJae)
|
abnormal cell physiology
|
J:188600
|
decreased fibroblast proliferation
|
J:188600
|
decreased sensitivity to induced cell death
|
J:188600
|
Dph1tm2Bhr/Dph1tm2Bhr
(either: 129/Sv or (involves: 129/Sv * C57BL/6))
|
abnormal cell cycle
|
J:88090
|
Dph1tm2Bhr/Dph1tm2Bhr Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129/Sv * C57BL/6)
|
cellular phenotype
|
J:88090
|
Dph3tm1Lepp/Dph3tm1Lepp
(involves: 129S1/Sv * C57BL/6)
|
increased neural tube apoptosis
|
J:109066
|
Dpp3tm1d(EUCOMM)Hmgu/Dpp3tm1d(EUCOMM)Hmgu
(involves: BALB/c * C57BL/6 * C57BL/6J * C57BL/6N * SJL)
|
decreased apoptosis
|
J:294242
|
Dppa2tm1.1Reik/Dppa2+ Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
(involves: C57BL/6 * FVB/N)
|
maternal effect
|
J:316936
|
Dppa2tm1.1Yam/Dppa2tm1.1Yam Dppa4tm1Yam/Dppa4tm1Yam
(involves: 129S4/SvJae)
|
abnormal DNA methylation
|
J:178324
|
decreased cell proliferation
|
J:178324
|
Dppa2tm2.1Reik/Dppa2tm2.1Reik Dppa4tm2.1Reik/Dppa4tm2.1Reik Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
(involves: C57BL/6 * FVB/N)
|
maternal effect
|
J:316936
|
Dppa3tm1(rtTA)Nkn/Dppa3tm1(rtTA)Nkn
(involves: 129S2/SvPas * C57BL/6)
|
abnormal DNA methylation
|
J:189990
|
Dppa3tm1Masu/Dppa3tm1Masu
(involves: 129S/SvEv)
|
maternal effect
|
J:86824
|
Dppa4tm1.1Hjf/Dppa4tm1.1Hjf
(B6.129P2-Dppa4tm1.1Hjf)
|
maternal effect
|
J:149143
|
Dppa4tm1.1Reik/Dppa4+ Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
(involves: C57BL/6 * FVB/N)
|
maternal effect
|
J:316936
|
Dppa4tm1.2Reik/Dppa4+
(involves: C57BL/6 * FVB/N)
|
maternal effect
|
J:316936
|
Dpy19l2tm1Lex/Dpy19l2tm1Lex
(B6;129S5-Dpy19l2tm1Lex/Mmucd)
|
abnormal acrosome morphology
|
J:187630
|
abnormal male germ cell morphology
|
J:187630
|
abnormal manchette morphology
|
J:187630
|
abnormal sperm midpiece morphology
|
J:187630
|
abnormal sperm mitochondrial sheath morphology
|
J:187630
|
abnormal sperm principal piece morphology
|
J:187630
|
absent sperm mitochondrial sheath
|
J:187630
|
coiled sperm flagellum
|
J:187630
|
detached acrosome
|
J:187630
|
ectopic manchette
|
J:187630
|
elongated manchette
|
J:187630
|
globozoospermia
|
J:187630
|
multiflagellated sperm
|
J:187630
|
Dpysl3Gt(IST14728H3)Tigm/Dpysl3Gt(IST14728H3)Tigm
(C57BL/6-Dpysl3Gt(IST14728H3)Tigm)
|
abnormal axon extension
|
J:223415
|
abnormal neuron differentiation
|
J:223415
|
Drc1em1Mngx/Drc1em1Mngx
(involves: C57BL/6)
|
abnormal respiratory motile cilium physiology
|
J:322334
|
Drc1em1Mngx/Drc1em1Mngx
(involves: C57BL/6 * ICR)
|
absent sperm flagellum
|
J:322334
|
oligozoospermia
|
J:322334
|
short sperm flagellum
|
J:322334
|
Drc1em2Mngx/Drc1em2Mngx
(involves: C57BL/6 * ICR)
|
abnormal manchette morphology
|
J:322334
|
abnormal respiratory motile cilium morphology
|
J:322334
|
abnormal respiratory motile cilium physiology
|
J:322334
|
abnormal sperm axoneme morphology
|
J:322334
|
abnormal sperm flagellum morphology
|
J:322334
|
abnormal sperm head morphology
|
J:322334
|
abnormal sperm radial spoke morphology
|
J:322334
|
absent sperm flagellum
|
J:322334
|
coiled sperm flagellum
|
J:322334
|
immotile sperm
|
J:322334
|
kinked sperm flagellum
|
J:322334
|
oligozoospermia
|
J:322334
|
short sperm flagellum
|
J:322334
|
thick sperm flagellum
|
J:322334
|
Drc1em3Mngx/Drc1em3Mngx
(involves: C57BL/6 * ICR)
|
abnormal manchette morphology
|
J:322334
|
abnormal respiratory motile cilium morphology
|
J:322334
|
abnormal respiratory motile cilium physiology
|
J:322334
|
abnormal sperm axoneme morphology
|
J:322334
|
abnormal sperm flagellum morphology
|
J:322334
|
abnormal sperm head morphology
|
J:322334
|
abnormal sperm radial spoke morphology
|
J:322334
|
absent sperm flagellum
|
J:322334
|
coiled sperm flagellum
|
J:322334
|
immotile sperm
|
J:322334
|
kinked sperm flagellum
|
J:322334
|
oligozoospermia
|
J:322334
|
short sperm flagellum
|
J:322334
|
thick sperm flagellum
|
J:322334
|
Drc7tm1.1Osb/Drc7tm1.1Osb
(involves: C57BL/6NSlc * DBA/2)
|
abnormal manchette morphology
|
J:284740
|
abnormal sperm axoneme morphology
|
J:284740
|
abnormal sperm flagellum morphology
|
J:284740
|
abnormal sperm head morphology
|
J:284740
|
abnormal sperm mitochondrial sheath morphology
|
J:284740
|
cellular phenotype
|
J:284740
|
decreased elongated spermatid number
|
J:284740
|
immotile sperm
|
J:284740
|
oligozoospermia
|
J:284740
|
short sperm flagellum
|
J:284740
|
Drd1tm1Jcd/Drd1tm1Jcd
(involves: 129S4/SvJae)
|
abnormal neuronal migration
|
J:121219
|
Drd2tm1Ebo/Drd2tm1Ebo
(involves: 129S2/SvPas * C57BL/6)
|
increased susceptibility to neuronal excitotoxicity
|
J:65767
|
Drd2tm1Ebo/Drd2tm1Ebo
(B6.129S2-Drd2tm1Ebo)
|
increased susceptibility to neuronal excitotoxicity
|
J:65767
|
Drd2tm1Low/Drd2tm1Low
(B6.129S2-Drd2tm1Low/J)
|
abnormal neuronal migration
|
J:121219
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:194407
|
Droshatm1Litt/Droshatm1Litt Tg(KRT5-rtTA)1Glk/0 Tg(tetO-cre)1Jaw/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
increased apoptosis
|
J:183487
|
Droshatm1Litt/Droshatm1Litt Tg(Six2-EGFP/cre)1Amc/0
(involves: 129P2/OlaHsd * CD-1)
|
increased kidney apoptosis
|
J:321428
|
Dsc1tm1Dga/Dsc1tm1Dga
(involves: C57BL/6J)
|
abnormal keratinocyte differentiation
|
J:73102
|
Dsc2tm1.2Leu/Dsc2tm1.2Leu
(involves: C57BL/6)
|
increased apoptosis
|
J:302593
|
Dsc3tm2Pko/Dsc3tm2Pko Tg(KRT14-cre)1Amc/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
decreased keratinocyte adhesion
|
J:140129
|
Dscam2J/Dscam2J
(C3H/HeDiSn-Dscam2J/GrsrJ)
|
abnormal axon fasciculation
|
J:179393
|
Dscamtm1.1Pfu/Dscamtm1.1Pfu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal axon fasciculation
|
J:179393
|
Dscamtm1Pfu/Dscamtm1Pfu Gt(ROSA)26Sortm3(CAG-EGFP/Dsred2)Luo/? Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal axon fasciculation
|
J:179393
|
Dscamtm1Pfu/Dscamtm1Pfu Opn4tm1(cre)Sapa/Opn4+
(involves: 129 * C57BL/6)
|
abnormal axon fasciculation
|
J:179393
|
Dscamtm1Pfu/Dscamtm1Pfu Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal axon fasciculation
|
J:179393
|
Dscamtm1Pfu/Dscamtm1Pfu Tg(Pax6-cre,GFP)2Pgr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal axon fasciculation
|
J:179393
|
Dsg2em1Spin/Dsg2+
(involves: C57BL/6J)
|
decreased keratinocyte adhesion
|
J:342765
|
Dsg2em1Spin/Dsg2em1Spin
(involves: C57BL/6J)
|
abnormal cell adhesion
|
J:342765
|
decreased keratinocyte adhesion
|
J:342765
|
Dsg2tm1d(EUCOMM)Wtsi/Dsg2tm1d(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
increased cardiomyocyte apoptosis
|
J:235770
|
Dsg2tm1Leu/Dsg2tm1Leu
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal cell death
|
J:102536
|
decreased fibroblast proliferation
|
J:102536
|
Dsg3tm1Stan/Dsg3tm1Stan
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal cell adhesion
|
J:40804
|
Dsptm1Efu/Dsptm1Efu Mnx1tm4(cre)Tmj/Mnx1+
(either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
delayed axon extension
|
J:219630
|
Dsptm1Efu/Dsptm1Efu Myl2tm1(cre)Krc/Myl2+
(involves: 129 * 129S4/SvJae * C57BL/6)
|
increased apoptosis
|
J:205990
|
Dsptm1Efu/Dsptm1Efu Tg(KRT14-cre)1Efu/0
(involves: 129)
|
abnormal cell adhesion
|
J:67797
|
Dspd/Dspd+
(involves: C3H * C57BL/6)
|
abnormal sperm head morphology
|
J:89381
|
oligozoospermia
|
J:89381
|
Dspptm1Kul/Dspptm1Kul
(involves: 129/Sv * C57BL/6)
|
increased kidney apoptosis
|
J:113417
|
DstTg4/DstTg4
(involves: CD-1)
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:55704
|
Dstncorn1/Dstncorn1
(A.BY-H2bc H2-T18f/SnJ)
|
increased cell proliferation
|
J:31798
|
Dtx1tm1.1Mzl/Dtx1tm1.1Mzl Tg(Cd4-cre)1Cwi/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased T cell proliferation
|
J:151605
|
Dtx1tm1.2Mzl/Dtx1tm1.2Mzl
(B6.129-Dtx1tm1.2Mzl)
|
decreased thymocyte apoptosis
|
J:151605
|
increased B cell proliferation
|
J:151605
|
increased T cell proliferation
|
J:151605
|
Dusp1tm1Brv/Dusp1tm1Brv
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cellular respiration
|
J:129718
|
abnormal myoblast differentiation
|
J:162340
|
decreased myoblast proliferation
|
J:162340
|
Dusp1tm1Brv/Dusp1tm1Brv
(involves: 129S2/SvPas * various)
|
increased mast cell degranulation
|
J:125919
|
Dusp1tm1Brv/Dusp1tm1Brv
(B6.129S2-Dusp1tm1Brv)
|
increased neuron apoptosis
|
J:163234
|
Dusp4Gt(XG164)Byg/Dusp4Gt(XG164)Byg
(B6.129P2-Dusp4Gt(XG164)Byg)
|
increased T cell proliferation
|
J:180366
|
Dusp4tm1Jmol/Dusp4tm1Jmol
(involves: 129)
|
decreased B cell apoptosis
|
J:140567
|
Dusp5tm1.1Achn/Dusp5tm1.1Achn
(involves: C57BL/6NCrl)
|
increased T cell proliferation
|
J:218203
|
Dusp5tm1a(KOMP)Wtsi/Dusp5tm1a(KOMP)Wtsi
(C57BL/6-Dusp5tm1a(KOMP)Wtsi)
|
increased T cell apoptosis
|
J:240637
|
increased T cell proliferation
|
J:240637
|
Dusp5tm1d(KOMP)Wtsi/Dusp5tm1d(KOMP)Wtsi
(B6(Cg)-Dusp5tm1d(KOMP)Wtsi)
|
increased T cell apoptosis
|
J:240637
|
Dusp6tm1Jmol/Dusp6tm1Jmol
(involves: 129 * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:142966
|
Dusp10tm1Flv/Dusp10tm1Flv
(involves: 129S6/SvEvTac)
|
decreased T cell proliferation
|
J:92104
|
Dusp14Gt(OST210117)Lex/Dusp14Gt(OST210117)Lex
(B6.129S5-Dusp14Gt(OST210117)Lex)
|
increased T cell proliferation
|
J:209403
|
Dusp22tm1Tht/Dusp22tm1Tht
(B6.129S7-Dusp22tm1Tht)
|
decreased B cell proliferation
|
J:213253
|
increased T cell proliferation
|
J:213253
|
DymGt(GTR1.3)1Rul/DymGt(GTR1.3)1Rul
(involves: 129)
|
abnormal intracellular organelle morphology
|
J:141099
|
abnormal vesicle-mediated transport
|
J:141099
|
Dync1h1tm1.1Ics/Dync1h1+
(involves: C57BL/6 * C57BL/6N * SJL)
|
abnormal cell proliferation
|
J:334549
|
abnormal mitosis
|
J:334549
|
abnormal neuronal migration
|
J:334549
|
abnormal radial glial cell morphology
|
J:334549
|
increased neuron apoptosis
|
J:334549
|
Dync1li1m1Emcf/Dync1li1m1Emcf
(involves: BALB/cAnNCrl * C3H/HeH * C57BL/6)
|
abnormal lysosome physiology
|
J:171267
|
abnormal neuronal migration
|
J:171267
|
Dync2h1pol/Dync2h1pol
(involves: C3H/HeJ * C57BL/6J)
|
abnormal motile primary cilium morphology
|
J:309102
|
Dync2h1ttn/Dync2h1ttn
(Not Specified)
|
abnormal cilium morphology
|
J:138139
|
Dync2i1Tn(pb-Act-RFP)1.1Zhu/Dync2i1Tn(pb-Act-RFP)1.1Zhu
(involves: FVB/NJ)
|
abnormal cilium morphology
|
J:335806
|
Dync2i2tm1Blnw/Dync2i2tm1Blnw
(involves: 129S6/SvEvTac * C57BL/6 * Swiss Webster)
|
abnormal embryonic neuroepithelium primary cilium morphology
|
J:242833
|
abnormal microtubule cytoskeleton morphology
|
J:242833
|
abnormal primary cilium morphology
|
J:242833
|
Dync2i2Tn(pb-Act-RFP)1.1Zhu/Dync2i2Tn(pb-Act-RFP)1.1Zhu
(involves: C57BL/6 * FVB/NJ)
|
abnormal cilium morphology
|
J:335806
|
Dync2li1tm1Aar/Dync2li1tm1Aar
(involves: 129P2/OlaHsd)
|
abnormal motile primary cilium morphology
|
J:93573
|
absent embryonic cilia
|
J:93573
|
decreased embryonic cilium length
|
J:93573
|
Dynll1Gt(EUCE0287d04)Hmgu/Dynll1Gt(EUCE0287d04)Hmgu
(involves: 129P2/OlaHsd)
|
abnormal embryonic neuroepithelium primary cilium morphology
|
J:217609
|
abnormal primary cilium morphology
|
J:217609
|
decreased embryonic cilium length
|
J:217609
|
Dynlrb1tm1a(EUCOMM)Wtsi/Dynlrb1+ Tg(Thy1-YFP)16Jrs/0
(involves: C57BL/6J * C57BL/6N)
|
abnormal axon extension
|
J:292124
|
Dynlt2a1tm1June/Dynlt2a1tm1June
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal male germ cell apoptosis
|
J:162909
|
abnormal sperm flagellum morphology
|
J:162909
|
abnormal sperm head morphology
|
J:162909
|
asthenozoospermia
|
J:162909
|
multiflagellated sperm
|
J:162909
|
oligozoospermia
|
J:162909
|
Dynlt2bem1Ktmr/Dynlt2bem1Ktmr
(C57BL/6N-Dynlt2bem1Ktmr)
|
abnormal outer dense fiber morphology
|
J:361529
|
abnormal sperm axoneme morphology
|
J:361529
|
abnormal sperm fibrous sheath morphology
|
J:361529
|
abnormal sperm flagellum morphology
|
J:361529
|
cellular phenotype
|
J:361529
|
coiled sperm flagellum
|
J:361529
|
decreased elongated spermatid number
|
J:361529
|
immotile sperm
|
J:361529
|
oligozoospermia
|
J:361529
|
Dyrk1atm1Jdc/Dyrk1atm1Jdc Tg(Mx1-cre)1Cgn/0
(involves: 129/Sv * C57BL/6J * C57BL/6NTac * CBA/J)
|
abnormal cell cycle
|
J:223138
|
increased T cell apoptosis
|
J:223138
|
Dyrk2tm1.1Kyos/Dyrk2tm1.1Kyos
(involves: C57BL/6J * C57BL/6N)
|
abnormal primary cilium morphology
|
J:298652
|
Dzip1em1Sasl/Dzip1+
(C57BL/6J-Dzip1em1Sasl)
|
abnormal motile cilium morphology
|
J:291454
|
Dzip1em1Yxc/Dzip1em1Yxc
(Not Specified)
|
absent sperm flagellum
|
J:333286
|
asthenozoospermia
|
J:333286
|
oligozoospermia
|
J:333286
|
teratozoospermia
|
J:333286
|
Dzip1tm1.1Blnw/Dzip1tm1.1Blnw
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal primary cilium morphology
|
J:207249
|
E2f1Tg(Wnt1-cre)2Sor/E2f1+ Snrpbem1Lajm/Snrpb+
(involves: C3H * C57BL/6 * C57BL/6J * CD1)
|
abnormal DNA-templated transcription
|
J:326544
|
E2f1tm1.1Dgj/E2f1tm1.1Dgj
(involves: FVB)
|
abnormal base-excision repair
|
J:212453
|
abnormal double-strand DNA break repair
|
J:212453
|
cellular phenotype
|
J:212453
|
E2f1tm1Meg/E2f1tm1Meg
(either: (involves: 129/Sv * 129S4/SvJae) or (involves: 129/Sv * 129S4/SvJae * C57BL/6))
|
decreased apoptosis
|
J:33100
|
E2f1tm1Meg/E2f1tm1Meg
(NOD.Cg-E2f1tm1Meg)
|
abnormal cell cycle
|
J:93708
|
E2f1tm1Meg/E2f1tm1Meg
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell death
|
J:75726
|
decreased T cell proliferation
|
J:76318
|
E2f1tm1Meg/E2f1tm1Meg E2f2tm1Zubi/E2f2tm1Zubi E2f3tm2.1Gle/E2f3tm2.1Gle
(involves: 129 * FVB/N * NIH Black Swiss)
|
decreased cell proliferation
|
J:138289
|
E2f1tm1Meg/E2f1tm1Meg E2f2tm1Zubi/E2f2tm1Zubi E2f3tm3.1Gle/E2f3tm3.1Gle
(involves: 129 * FVB/N * NIH Black Swiss)
|
decreased cell proliferation
|
J:138289
|
E2f1tm1Meg/E2f1tm1Meg E2f3tm2.1Gle/E2f3tm2.1Gle
(involves: 129S4/SvJae * 129S6/SvEvTac * FVB/N * NIH Black Swiss)
|
decreased cell proliferation
|
J:138289
|
E2f1tm1Meg/E2f1tm1Meg Rb1tm1Tyj/Rb1tm1Tyj Tg(Rb1)1Blg/0
(involves: 129S2/SvPas * 129S4/SvJae)
|
abnormal cell cycle
|
J:65679
|
polyploidy
|
J:65679
|
E2f1tm1Meg/E2f1tm1Meg Rb1tm2.1Fad/Rb1tm2.1Fad
(involves: 129S4/SvJae * C57BL/6)
|
cellular phenotype
|
J:215358
|
E2f1tm1Njd/E2f1tm1Njd
(involves: 129S2/SvPas * C57BL/6)
|
abnormal fat cell differentiation
|
J:89720
|
increased adipocyte glucose uptake
|
J:89720
|
E2f1tm1Njd/E2f1tm1Njd E2f3tm2Lees/E2f3tm2Lees
(involves: 129S2/SvPas * 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:147270
|
decreased cell proliferation
|
J:147270
|
E2f2tm1Zubi/E2f2tm1Zubi
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell death
|
J:75726
|
abnormal cell physiology
|
J:75726
|
increased T cell proliferation
|
J:76318
|
E2f2tm1Zubi/E2f2tm1Zubi Tg(TcraH-Y,TcrbH-Y)71Vbo/?
(involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2J)
|
increased T cell proliferation
|
J:76318
|
E2f3tm1.2Gle/E2f3tm1.2Gle
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:75726
|
E2f3tm1Lees/E2f3+
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell physiology
|
J:65128
|
E2f3tm1Lees/E2f3tm1Lees
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell cycle
|
J:65128
|
abnormal cell physiology
|
J:65128
|
decreased cell proliferation
|
J:65128
|
E2f3tm2Lees/E2f3tm2Lees
(either: 129S/Sv-E2f3tm2Lees or (involves: 129S4/SvJae * C57BL/6))
|
abnormal cell cycle
|
J:147270
|
abnormal cell physiology
|
J:147270
|
E2f4tm1Jrn/E2f4tm1Jrn
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal colon goblet cell morphology
|
J:64192
|
abnormal small intestine goblet cell morphology
|
J:64192
|
E2f4tm1Jrn/E2f4tm1Jrn E2f5tm1Dli/E2f5tm1Dli
(involves: 129P2/OlaHsd * 129S1/Sv * BALB/c * C57BL/6)
|
abnormal cell cycle
|
J:64757
|
E2f4tm2.1Lees/E2f4tm2.1Lees Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6)
|
abnormal respiratory motile cilium morphology
|
J:241925
|
E2f4tm2.1Lees/E2f4tm2.1Lees Shhtm1(EGFP/cre)Cjt/Shh+
(involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6)
|
abnormal respiratory motile cilium morphology
|
J:241925
|
E2f6tm1Lees/E2f6tm1Lees
(involves: 129S4/SvJae * C57BL/6)
|
cellular phenotype
|
J:134271
|
E2f6tm1Sgau/E2f6tm1Sgau
(involves: 129S4/SvJae * C57BL/6)
|
cellular phenotype
|
J:106219
|
oligozoospermia
|
J:106219
|
E2f7tm1.1Gle/E2f7tm1.1Gle E2f8tm1.1Gle/E2f8tm1.1Gle
(involves: 129S6/SvEvTac * FVB/N)
|
increased embryonic tissue cell apoptosis
|
J:131292
|
E2f7tm1.1Gle/E2f7tm1.1Gle E2f8tm1.1Gle/E2f8tm1.1Gle
(involves: 129S6/SvEvTac)
|
increased placenta apoptosis
|
J:183999
|
E2f7tm1Gle/E2f7tm1Gle E2f8tm1Gle/E2f8tm1Gle
(involves: 129S6/SvEvTac * FVB/N)
|
increased cellular sensitivity to alkylating agents
|
J:131292
|
E4f1tm1Pisc/E4f1tm1Pisc
(involves: 129S4/SvJae * C57BL/6)
|
abnormal apoptosis
|
J:91435
|
abnormal mitosis
|
J:91435
|
Eamcd1A/WySn/Eamcd1A/WySn
(B10.A-(D1Mit65-D1Mit334))
|
decreased sensitivity to induced cell death
|
J:145043
|
Ebf1tm1.1Rug/Ebf1tm1.1Rug Polr2atm1(cre/ERT2)Bbd/Polr2a+
(involves: C57BL/6 * SJL)
|
decreased B cell proliferation
|
J:182210
|
increased B cell apoptosis
|
J:182210
|
Ebf2tm2(Zfp423)Reed/Ebf2+ Omptm4(cre)Mom/Omp+
(involves: 129 * 129P2/OlaHsd * C57BL/10J)
|
impaired neuron differentiation
|
J:190934
|
Ebf2tm2.1(Zfp423)Reed/Ebf2+
(involves: 129 * C57BL/10J)
|
impaired neuron differentiation
|
J:190934
|
Ecel1em1Hiki/Ecel1em1Hiki Tg(Hlxb9-GFP)1Tmj/0
(involves: C57BL/6 * CBA)
|
abnormal axon guidance
|
J:260240
|
Ecel1em2Hiki/Ecel1em2Hiki Tg(Hlxb9-GFP)1Tmj/0
(involves: C57BL/6 * CBA)
|
abnormal axon guidance
|
J:260240
|
Ecscrtm1Iked/Ecscrtm1Iked
(Not Specified)
|
abnormal vascular endothelial cell migration
|
J:173348
|
decreased vascular endothelial cell apoptosis
|
J:173348
|
Ecsittm1Gho/Ecsittm1Gho
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased cell proliferation
|
J:86912
|
Edardl/Edardl
(involves: A/H)
|
increased apoptosis
|
J:116222
|
Edil3Tg(lacZ)1Tq/Edil3Tg(lacZ)1Tq
(Not Specified)
|
increased chondrocyte apoptosis
|
J:254384
|
Edil3Tg(Sox2-cre)1Amc/Edil3+ Tgif1tm1Caw/Tgif1tm1Caw Tgif2tm1Dwot/Tgif2tm1Dwot
(involves: 129S/SvEv * C57BL/6 * C57BL/6J * CBA)
|
increased apoptosis
|
J:183402
|
Edil3tm1Tq/Edil3tm1Tq
(B6.129S6-Edil3tm1Tq)
|
abnormal cellular extravasation
|
J:141063
|
abnormal leukocyte adhesion
|
J:141063
|
enhanced leukocyte tethering or rolling
|
J:141063
|
Edil3tm1Tq/Edil3tm1Tq Itgaltm1Bll/Itgaltm1Bll
(involves: 129 * C57BL/6)
|
abnormal cellular extravasation
|
J:141063
|
Edn2tm1Ywa/Edn2tm1Ywa
(involves: 129S6/SvEvTac * C57BL/6)
|
impaired luteal cell differentiation
|
J:215159
|
Ednratm1Ywa/Ednratm1Ywa
(129S/SvEv-Ednratm1Ywa)
|
patent ductus arteriosus
|
J:46639
|
Ednrbs-36Pub/Ednrbs-36Pub
(B6.Cg-Ednrbs-36Pub)
|
increased cell proliferation
|
J:125229
|
increased mitotic index
|
J:125229
|
Ednrbs-l/Ednrbs-l
(involves: C57BL/6J * SSL/Le)
|
abnormal melanocyte proliferation
|
J:19441
|
Ednrbtm1Myks/Ednrbtm1Myks
(involves: 129P2/OlaHsd)
|
abnormal cell migration
|
J:84057
|
Ednrbtm1Nrd/Ednrbtm1Nrd Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/J)
|
abnormal enteric neural crest cell migration
|
J:140320
|
Ednrbtm1Nrd/Ednrbtm1Nrd Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ Tg(Tyr-cre/ERT2)13Bos/0
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J)
|
abnormal melanocyte proliferation
|
J:231435
|
Ednrbtm1Ywa/Ednrbtm1Ywa
(B6;129-Ednrbtm1Ywa/J)
|
abnormal colon goblet cell morphology
|
J:216833
|
Eef1a2wst/Eef1a2wst
(B6C3Fe a/a-Eef1a2wst/J)
|
chromosomal instability
|
J:6766
|
increased cellular sensitivity to gamma-irradiation
|
J:6766
|
Eef1dtm1.2Mkma/Eef1dtm1.2Mkma
(B6J.B6N(Cg)-Eef1dtm1.2Mkma)
|
abnormal translation
|
J:288930
|
increased endoplasmic reticulum stress
|
J:288930
|
Eef1e1Gt(OST377244)Lex/Eef1e1+
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell cycle
|
J:96923
|
decreased splenocyte apoptosis
|
J:96923
|
increased cell proliferation
|
J:96923
|
increased splenocyte proliferation
|
J:96923
|
Eef2tm1.1Lepp/Eef2+
(involves: C57BL/6)
|
decreased sensitivity to induced cell death
|
J:188600
|
Eef2tm1.1Lepp/Eef2tm1.1Lepp
(involves: C57BL/6)
|
abnormal cell physiology
|
J:188600
|
cellular phenotype
|
J:188600
|
decreased sensitivity to induced cell death
|
J:188600
|
Eef2ktm1.1Cgpd/Eef2ktm1.1Cgpd
(involves: C57BL/6)
|
decreased sensitivity to induced cell death
|
J:224568
|
Eef2ktm1Agry/Eef2ktm1Agry
(B6.Cg-Eef2ktm1Agry)
|
abnormal oocyte morphology
|
J:208406
|
decreased apoptosis
|
J:208406
|
Efcab9em1Chng/Efcab9em1Chng
(involves: C57BL/6)
|
abnormal sperm flagellum morphology
|
J:276402
|
abnormal sperm motility
|
J:276402
|
Efemp2tm1.2Hiya/Efemp2tm1.2Hiya
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased vascular endothelial cell apoptosis
|
J:170883
|
increased vascular endothelial cell proliferation
|
J:170883
|
increased vascular smooth muscle cell proliferation
|
J:170883
|
Efhc1tm1Kzy/Efhc1tm1Kzy
(B6.129P2-Efhc1tm1Kzy)
|
abnormal brain ependyma motile cilium physiology
|
J:145858
|
Efhd1em1Wei/Efhd1em1Wei
(Not Specified)
|
abnormal axon extension
|
J:305107
|
increased neuron apoptosis
|
J:305107
|
Efna2tm1Jgf/Efna2tm1Jgf
(involves: 129/Sv * C57BL/6)
|
abnormal neuron differentiation
|
J:96025
|
Efna5tm1Wrst/Efna5tm1Wrst
(Not Specified)
|
abnormal neuronal migration
|
J:79997
|
Efnb1tm1.1Jwu/Efnb1tm1.1Jwu Efnb2tm1.1Jwu/Efnb2tm1.1Jwu Tg(Lck-cre)I540Jxm/0
(B6.Cg-Efnb2tm1.1Jwu Efnb1tm1.1Jwu Tg(Lck-cre)I540Jxm)
|
increased thymocyte apoptosis
|
J:178148
|
Efnb1tm1.1Sor/Efnb1tm1.1Sor
(involves: 129S4/SvJaeSor)
|
abnormal cardiac neural crest cell migration
|
J:89008
|
abnormal cranial neural crest cell migration
|
J:89008
|
Efnb2tm1Henk/Efnb2tm1Henk
(either: 129 or (involves: 129 * C57BL/6) or (involves: 129 * CD-1))
|
abnormal axon guidance
|
J:91492
|
Efnb2tm1Kln/Efnb2tm1Kln
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal neural crest cell migration
|
J:67296
|
Efnb2tm2Sor/Efnb2tm2Sor
(involves: 129S4/SvJaeSor * C57BL/6J)
|
abnormal cranial neural crest cell migration
|
J:143845
|
abnormal trunk neural crest cell migration
|
J:143845
|
increased cranial neural crest cell apoptosis
|
J:143845
|
Efnb3tm1.1Henk/Efnb3tm1.1Henk
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon pruning
|
J:150550
|
Efnb3tm1Henk/Efnb3tm1Henk
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon pruning
|
J:150550
|
Efnb3tm2.1Henk/Efnb3tm2.1Henk
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon pruning
|
J:150550
|
Efnb3tm3.1Henk/Efnb3tm3.1Henk
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon pruning
|
J:150550
|
Efr3atm1Bgsn/Efr3atm1Bgsn Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6J * SJL)
|
decreased neuron apoptosis
|
J:273433
|
premature neuronal precursor differentiation
|
J:273433
|
Egfrtm2(EGFR)Wag/Egfrtm2(EGFR)Wag
(involves: 129/Sv * C57BL/6)
|
enhanced osteoblast differentiation
|
J:84870
|
EgfrVel/Egfr+
(involves: C57BL/6J)
|
decreased fibroblast cell migration
|
J:88776
|
Egln1tm1.1Brei/Egln1tm1.1Brei Myl2tm1(cre)Krc/Myl2+
(B6.Cg-Myl2tm1(cre)Krc Egln1tm1.1Brei)
|
decreased cardiomyocyte apoptosis
|
J:170943
|
Egln1tm1Kael/Egln1tm1Kael Egln3tm1Vlcg/Egln3tm1Vlcg Tg(Myh6-cre)2182Mds/0
(involves: 129S6/SvEvTac * FVB/N)
|
decreased mitochondrial number
|
J:179490
|
Egln1tm1Kael/Egln1tm1Kael Tg(Myh6-cre)2182Mds/0
(involves: 129S6/SvEvTac * FVB/N)
|
cardiac interstitial fibrosis
|
J:179490
|
decreased mitochondrial number
|
J:179490
|
Egln2tm1Pec/Egln2tm1Pec
(involves: 129S/SvEv * Swiss)
|
abnormal mitochondrial physiology
|
J:132630
|
Egln3tm1Pjr/Egln3tm1Pjr
(involves: 129S/SvEv * Swiss)
|
decreased neuron apoptosis
|
J:136034
|
Egr1tm1Jmi/Egr1tm1Jmi
(involves: 129 * C57BL/6)
|
abnormal mitosis
|
J:93996
|
decreased mitotic index
|
J:93996
|
Egr1tm1Jmi/Egr1tm1Jmi Tg(Defcr2-TAg)#Jig/?
(involves: 129 * C57BL/6 * FVB/N)
|
cellular phenotype
|
J:67125
|
Egr1tm1Pch/Egr1tm1Pch
(involves: 129S2/SvPas * C57BL/6J)
|
oligozoospermia
|
J:45064
|
Egr2tm1.1Jchn/Egr2tm1Pch
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
abnormal neuronal migration
|
J:82071
|
Egr2tm1Jmi/Egr2tm1Jmi
(Not Specified)
|
increased Schwann cell proliferation
|
J:96641
|
Egr2tm4Pch/Egr2tm4Pch
(involves: BALB/c * C57BL/6)
|
increased Schwann cell proliferation
|
J:137156
|
Egr4tm1Jmi/Egr4tm1Jmi
(involves: C57BL/6)
|
abnormal male meiosis
|
J:58099
|
abnormal sperm flagellum morphology
|
J:58099
|
abnormal sperm head morphology
|
J:58099
|
coiled sperm flagellum
|
J:58099
|
decreased male germ cell number
|
J:58099
|
detached sperm flagellum
|
J:58099
|
increased male germ cell apoptosis
|
J:58099
|
kinked sperm flagellum
|
J:58099
|
oligozoospermia
|
J:58099
|
teratozoospermia
|
J:58099
|
Ehd1tm1.2Haba/Ehd1tm1.2Haba
(involves: 129P2/OlaHsd * C57BL/6J * FVB/N)
|
abnormal acrosome morphology
|
J:160452
|
abnormal germ cell morphology
|
J:160452
|
abnormal male meiosis
|
J:160452
|
abnormal spermatid morphology
|
J:160452
|
abnormal spermatocyte morphology
|
J:160452
|
abnormal spermatogonia morphology
|
J:160452
|
azoospermia
|
J:160452
|
increased male germ cell apoptosis
|
J:160452
|
Ehd1tm1Mhor/Ehd1tm1Mhor
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Swiss Webster))
|
abnormal cell physiology
|
J:121819
|
cellular phenotype
|
J:121819
|
Ehd1tm1Mhor/Ehd1tm1Mhor
(involves: 129S6/SvEvTac)
|
abnormal cell migration
|
J:120764
|
decreased fibroblast cell migration
|
J:120764
|
Ehd2tm1.1Cbm/Ehd2tm1.1Cbm
(B6N.129(Cg)-Ehd2tm1.1Cbm)
|
abnormal fibroblast physiology
|
J:285350
|
increased adipocyte glucose uptake
|
J:285350
|
Ehd3tm1.2Haba/Ehd3tm1.2Haba Ehd4tm1.1Haba/Ehd4tm1.1Haba
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J)
|
increased renal glomerulus apoptosis
|
J:171715
|
mesangial cell interposition
|
J:171715
|
Ehd4tm1.1Haba/Ehd4tm1.1Haba
(involves: C57BL/6 * C57BL/6J * FVB/N)
|
abnormal spermatid morphology
|
J:160188
|
decreased male germ cell number
|
J:160188
|
increased cell proliferation
|
J:160188
|
increased male germ cell apoptosis
|
J:160188
|
oligozoospermia
|
J:160188
|
Ehhadhtm1Jkr/Ehhadhtm1Jkr
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal peroxisome physiology
|
J:55395
|
Ehhadhtm1Jkr/Ehhadhtm1Jkr Hsd17b4tm1Baes/Hsd17b4tm1Baes
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:89945
|
abnormal peroxisome morphology
|
J:89945
|
Ehmt1tm1.1Tara/Ehmt1tm1.1Tara Tg(Adipoq-cre)1Evdr/0
(involves: 129P2/OlaHsd * FVB/NJ)
|
decreased fatty acid oxidation
|
J:207678
|
Ehmt1tm1Bzhu/Ehmt1tm1Bzhu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal epigenetic regulation of gene expression
|
J:219788
|
Ehmt2Gt(ES62)Feil/Ehmt2Gt(ES62)Feil
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal imprinting
|
J:130398
|
Ehmt2tm1.1Cza/Ehmt2tm1.1Cza Tg(VAV1-cre)1Graf/0
(involves: C57BL/6 * SJL)
|
abnormal intestinal goblet cell morphology
|
J:160938
|
Ehmt2tm1Yshk/Ehmt2tm1Yshk
(B6.Cg-Ehmt2tm1Yshk)
|
abnormal apoptosis
|
J:77998
|
abnormal cell physiology
|
J:77998
|
Ei24tm1Hzha/Ei24tm1Hzha Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA)
|
abnormal hepatocyte mitochondrial morphology
|
J:193420
|
impaired autophagy
|
J:193420
|
Ei24tm1Hzha/Ei24tm1Hzha Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
impaired autophagy
|
J:193420
|
increased neuron apoptosis
|
J:193420
|
Eif2ak2tm1Ajs/Eif2ak2tm1Ajs
(involves: 129)
|
abnormal cell physiology
|
J:187314
|
Eif2ak2tm1Cwe/Eif2ak2tm1Cwe
(involves: 129S/SvEv * C57BL/6)
|
increased T cell proliferation
|
J:66112
|
Eif2ak2tm1Cwe/Eif2ak2tm1Cwe NipblGt(RRS564)Byg/Nipbl+
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6J * CD-1)
|
abnormal chromosome number
|
J:297059
|
abnormal DNA repair
|
J:297059
|
Eif2ak2tm1Jcbe/Eif2ak2tm1Jcbe
(involves: 129S4/SvJae * BALB/c)
|
cellular phenotype
|
J:53258
|
Eif2ak2tm1Jcbe/Eif2ak2tm1Jcbe
(involves: 129S4/SvJae)
|
decreased sensitivity to induced cell death
|
J:63671
|
increased sensitivity to induced cell death
|
J:63671
|
Eif2ak3tm1Drc/Eif2ak3tm1Drc
(involves: 129S6/SvEvTac)
|
abnormal osteoblast physiology
|
J:76661
|
increased osteoblast apoptosis
|
J:76661
|
Eif2ak3tm1Dron/Eif2ak3+ Tg(GFAP-tTA)110Pop/0 Tg(tetO-Ifng)184Pop/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2 * Swiss Webster)
|
abnormal oligodendrocyte apoptosis
|
J:99655
|
increased spinal cord apoptosis
|
J:99655
|
Eif2ak3tm1Dron/Eif2ak3tm1Dron
(involves: 129S6/SvEvTac)
|
abnormal cell physiology
|
J:124971
|
Eif2ak4tm1Drc/Eif2ak4tm1Drc
(involves: 129S6/SvEvTac * C57BL/6)
|
maternal effect
|
J:78945
|
Eif2b4tm1.1Vdk/Eif2b4tm1.1Vdk Eif2b5tm1.1Vdk/Eif2b5tm1.1Vdk
(involves: C57BL/6 * C57BL/6J)
|
increased oligodendrocyte progenitor number
|
J:234659
|
Eif2s2Gt(XH413)Byg/Eif2s2+
(129-Eif2s2Gt(XH413)Byg Chr 19MOLF/Ei)
|
decreased primordial germ cell proliferation
|
J:146879
|
X/Eif2s3yem2Asah
(involves: C57BL/6 * DBA/2)
|
abnormal spermatocyte morphology
|
J:244443
|
abnormal spermatogonia proliferation
|
J:244443
|
azoospermia
|
J:244443
|
decreased spermatid number
|
J:244443
|
X/Eif2s3yem#Asah
(involves: C57BL/6 * DBA/2)
|
abnormal spermatogonia proliferation
|
J:244443
|
azoospermia
|
J:244443
|
Eif3etm1Fshb/Eif3e+
(C57BL/6N-Eif3etm1Fshb)
|
abnormal translation
|
J:265010
|
cellular phenotype
|
J:265010
|
decreased fibroblast proliferation
|
J:265010
|
Eif3ftm1(KOMP)Vlcg/Eif3f+
(B6J.B6N-Eif3ftm1(KOMP)Vlcg)
|
abnormal translation
|
J:294674
|
Eif3hMommeD12/Eif3h+ Tg(HBA1-GFP)1Ew/0
(involves: C57BL/6J * FVB/NJ)
|
abnormal epigenetic regulation of gene expression
|
J:201509
|
Eif3hMommeD38/Eif3h+ Tg(HBA1-GFP)1Ew/0
(involves: C57BL/6J * FVB/NJ)
|
abnormal epigenetic regulation of gene expression
|
J:201509
|
Eif4a1tm1.1Bea/Eif4a1tm1.1Bea Tg(Fcer2a-cre)5Mbu/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased B cell proliferation
|
J:344730
|
Eif4e1bem1Dean/Eif4e1b+
(involves: C57BL/6 * DBA/2)
|
maternal effect
|
J:337681
|
Eif4e1bem1Glin/Eif4e1bem1Glin Tg(Zp3-cre)93Knw/0
(C57BL/6J-Eif4e1bem1Glin Tg(Zp3-cre)93Knw)
|
maternal effect
|
J:337006
|
Eif4e1bem2Dean/Eif4e1bem2Dean
(involves: C57BL/6 * DBA/2)
|
maternal effect
|
J:337681
|
Eif4e1bem3Dean/Eif4e1bem3Dean
(involves: C57BL/6 * DBA/2)
|
maternal effect
|
J:337681
|
Eif4eGt(RRO036)Byg/Eif4e+ Krastm3Tyj/Kras+
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB/N)
|
increased cellular sensitivity to oxidative stress
|
J:224214
|
oxidative stress
|
J:224214
|
Eif4etm1.1Lfur/Eif4etm1.1Lfur
(involves: 129X1/SvJ)
|
abnormal cell physiology
|
J:163589
|
Eif4eTn(pb-Act-RFP)1Xwu/Eif4eTn(pb-Act-RFP)1Xwu
(involves: FVB/NJ)
|
abnormal translation
|
J:308879
|
Eif4ebp1tm1Nso/Eif4ebp1tm1Nso
(involves: 129S4/SvJae * BALB/c)
|
abnormal cell physiology
|
J:72217
|
Eif4ebp1tm1Nso/Eif4ebp1tm1Nso Mtortm1.1Gcon/Mtortm1.1Gcon A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal autophagy
|
J:163763
|
abnormal mitochondrial physiology
|
J:163763
|
cardiac interstitial fibrosis
|
J:163763
|
decreased cardiomyocyte apoptosis
|
J:163763
|
Eif4g2tm1Yam/Eif4g2tm1Yam
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell differentiation
|
J:77324
|
Eif4g3Gt(XC431)Byg/Eif4g3repro8
(involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J)
|
arrest of male meiosis
|
J:159444
|
azoospermia
|
J:159444
|
Eif4g3repro8/Eif4g3repro8
(involves: C3HeB/FeJ * C57BL/6J)
|
arrest of male meiosis
|
J:159444
|
azoospermia
|
J:159444
|
increased male germ cell apoptosis
|
J:159444
|
Eif4g3repro8/Eif4g3repro8
(C3Fe.B6-Eif4g3repro8/Hand)
|
arrest of male meiosis
|
J:256976
|
Eif4hGt(Ex279)Byg/Eif4hGt(Ex279)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
maternal effect
|
J:181945
|
Eif5aGt(RRE174)Byg/Eif5aGt(RRE174)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cell proliferation
|
J:285882
|
Eif6tm1Sbif/Eif6+
(involves: 129 * C57BL/6)
|
abnormal cell physiology
|
J:141257
|
abnormal mitosis
|
J:141257
|
Elac2tm1c(EUCOMM)Wtsi/Elac2tm1c(EUCOMM)Wtsi Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6N * FVB)
|
abnormal cell physiology
|
J:265839
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:265839
|
abnormal mitochondrial physiology
|
J:265839
|
abnormal oxidative phosphorylation
|
J:265839
|
abnormal translation
|
J:265839
|
cellular phenotype
|
J:265839
|
Elapor1tm1Lex/Elapor1tm1Lex
(B6;129S5-Elapor1tm1Lex/Mmucd)
|
oligozoospermia
|
J:171883
|
teratozoospermia
|
J:171883
|
Elavl1tm1.1Atas/Elavl1tm1.1Atas Tnfrsf4tm2(cre)Nik/Tnfrsf4+
(involves: 129X1/SvJ * C57BL/6)
|
decreased T cell proliferation
|
J:207013
|
Elavl1tm1.1Bndr/Elavl1tm1.1Bndr Lyz2tm1(cre)Ifo/Lyz2+
(B6.129-Elavl1tm1.1Bndr)
|
cellular necrosis
|
J:182000
|
Elavl1tm1.1Dkon/Elavl1tm1.1Dkon Lyz2tm1(cre)Ifo/Lyz2+
(B6.129P2-Elavl1tm1.1Dkon Lyz2tm1(cre)Ifo)
|
abnormal macrophage chemotaxis
|
J:184388
|
Elavl1tm1.1Dkon/Elavl1tm1.1Dkon Tg(MYOD1-cre)M23Glh/0
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:279284
|
Elavl1tm1.1Thla/Elavl1+
(involves: 129S1/Sv)
|
increased cellular sensitivity to gamma-irradiation
|
J:155109
|
Elavl1tm1Thla/Elavl1tm1Thla Gt(ROSA)26Sortm1(cre/ERT2)Alj/Gt(ROSA)26Sor+
(involves: 129)
|
abnormal intestinal goblet cell morphology
|
J:155109
|
decreased B cell apoptosis
|
J:155109
|
decreased cell proliferation
|
J:155109
|
increased T cell apoptosis
|
J:155109
|
Elavl2tm1.2Ysa/Elavl2tm1.2Ysa
(involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
absent oocytes
|
J:282136
|
oocyte degeneration
|
J:282136
|
Elavl4tm1Okn/Elavl4tm1Okn
(Not Specified)
|
abnormal neuron differentiation
|
J:97282
|
increased neuron apoptosis
|
J:97282
|
Elf3tm1Pjh/Elf3tm1Pjh
(involves: 129S4/SvJae * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:76344
|
Elf4tm1Nim/Elf4tm1Nim
(B6.129S1-Elf4tm1Nim)
|
increased B cell proliferation
|
J:79568
|
increased T cell proliferation
|
J:79568
|
Elk1tm1Nor/Y
(involves: 129P2/OlaHsd * C57BL/6N)
|
asthenozoospermia
|
J:89763
|
Elmo1tm1.1Ravi/Elmo1tm1.1Ravi Tg(Amh-cre)8815Reb/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL)
|
increased male germ cell apoptosis
|
J:164662
|
oligozoospermia
|
J:164662
|
Elmo1tm1.2Ravi/Elmo1tm1.2Ravi
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal male germ cell apoptosis
|
J:164662
|
multinucleated giant male germ cells
|
J:164662
|
Elmod3em1Jili/Elmod3em1Jili
(involves: C57BL/6)
|
abnormal actin cytoskeleton morphology
|
J:293683
|
Eloatm1Aso/Eloatm1Aso
(involves: 129S/SvEv * C57BL/6)
|
decreased cell proliferation
|
J:119126
|
early cellular replicative senescence
|
J:119126
|
increased embryonic tissue cell apoptosis
|
J:119126
|
increased fibroblast apoptosis
|
J:119126
|
Eloatm1Aso/Eloatm1Aso Trp53tm1Sia/Trp53tm1Sia
(involves: 129S/SvEv * C57BL/6 * CBA)
|
increased embryonic tissue cell apoptosis
|
J:119126
|
Elof1tm1.1(KOMP)Vlcg/Elof1tm1.1(KOMP)Vlcg
(B6N(Cg)-Elof1tm1.1(KOMP)Vlcg/J)
|
decreased embryonic epiblast cell proliferation
|
J:277394
|
Elovl2tm1Jaco/Elovl2+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal sperm head morphology
|
J:168856
|
teratozoospermia
|
J:168856
|
Elovl4tm1Wked/Elovl4tm1Wked
(involves: 129S/SvEv * 129S1/Sv)
|
abnormal synaptic vesicle exocytosis
|
J:277065
|
Elovl4tm1Wked/Elovl4tm1Wked Tg(IVL-Elovl4)#Wked/0 Tg(KRT14-Elovl4)#Mpag/0
(involves: 129 * C57BL/6)
|
increased cellular glucose import
|
J:277065
|
Elovl6Gt(OST222498)Lex/Elovl6Gt(OST222498)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
decreased fatty acid oxidation
|
J:130031
|
Elp1tm1c(KOMP)Wtsi/Elp1tm1c(KOMP)Wtsi H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
abnormal neuron differentiation
|
J:202989
|
increased neuron apoptosis
|
J:202989
|
Elp1tm1c(KOMP)Wtsi/Elp1tm1c(KOMP)Wtsi Tg(Ddx4-cre)1Dcas/0
(involves: 129 * C57BL/6N * FVB)
|
abnormal chromosomal synapsis
|
J:200015
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:200015
|
abnormal double-strand DNA break repair
|
J:200015
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:200015
|
arrest of male meiosis
|
J:200015
|
azoospermia
|
J:200015
|
Elp2em2Bjw/Elp2em2Bjw
(involves: C57BL/6 * DBA/2J)
|
abnormal neuron differentiation
|
J:306113
|
Elp3tm1.1Tac/Elp3tm1.1Tac Tg(Vil1-cre)997Gum/0
(involves: C57BL/6 * C57BL/6J * C57BL/6NTac * SJL)
|
abnormal gastrointestinal brush cell morphology
|
J:227334
|
Emc1em1Xjz/Emc1em1Xjz Tg(Rho-icre)1Ck/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
increased retina apoptosis
|
J:345827
|
Emc10tm1.2Smoc/Emc10tm1.2Smoc
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL/J)
|
asthenozoospermia
|
J:307574
|
hairpin sperm flagellum
|
J:307574
|
kinked sperm flagellum
|
J:307574
|
oligozoospermia
|
J:307574
|
Emdtm1.1Stw/Y
(involves: 129S1/Sv * FVB/N)
|
cellular phenotype
|
J:106760
|
Emdtm1.1Stw/Emdtm1.1Stw
(involves: 129S1/Sv * FVB/N)
|
cellular phenotype
|
J:106760
|
Eme1Tn(pb-Act-RFP)1.1Zhu/Eme1+ Gen1Tn(pb-Act-RFP)1.1Zhu/Gen1Tn(pb-Act-RFP)1.1Zhu
(FVB/NJ-Eme1Tn(pb-Act-RFP)1.1Zhu Gen1Tn(pb-Act-RFP)1.1Zhu)
|
increased cellular sensitivity to DNA damaging agents
|
J:330453
|
Eme1Tn(pb-Act-RFP)1.1Zhu/Eme1+ Gen1Tn(pb-Act-RFP)1.1Zhu/Gen1Tn(pb-Act-RFP)1.1Zhu
(involves: C57BL/6J * FVB/NJ)
|
abnormal cell physiology
|
J:330453
|
Emg1tm1.1Btr/Emg1tm1.1Btr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
|
decreased cell proliferation
|
J:230556
|
increased apoptosis
|
J:230556
|
Emg1tm1Hdin/Emg1tm1Hdin
(involves: 129S1/Sv * 129X1/SvJ * CD-1 * ICR)
|
abnormal nucleolus morphology
|
J:165972
|
Eml1heco/?
(involves: CD-1)
|
abnormal mitotic spindle morphology
|
J:211342
|
abnormal neuronal precursor proliferation
|
J:211342
|
abnormal radial glial cell morphology
|
J:211342
|
increased neuron apoptosis
|
J:211342
|
Eml1tm1.2Ics/Eml1tm1.2Ics
(C57BL/6N-Eml1tm1.2Ics)
|
abnormal neuronal precursor proliferation
|
J:294769
|
Emx1tm1(cre)Ito/Emx1+ Hes1tm1Kag/Hes1tm1Kag Hes3tm1Kag/Hes3tm1Kag Hes5tm1Fgu/Hes5tm1Fgu
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal neuron differentiation
|
J:139170
|
Emx1tm1(cre)Ito/Emx1+ Tg(CAG-Mtor*)#Atai/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * ICR)
|
increased neuron apoptosis
|
J:211789
|
Emx1tm1(cre)Krj/Emx1+ Esco2tm1.1Ge/Esco2tm1.1Ge
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal neuronal precursor proliferation
|
J:180371
|
increased neuron apoptosis
|
J:180371
|
Emx1tm1(cre)Krj/Emx1+ Gsx2tm2.1Kc/Gsx2tm2.1Kc
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:154936
|
Emx1tm1(cre)Krj/Emx1+ Mycbp2tm1Adia/Mycbp2tm1Adia
(involves: 129S2/SvPas * C57BL/6)
|
abnormal axon guidance
|
J:125702
|
Emx1tm1(cre)Krj/Emx1+ Numbtm1Ynj/Numbtm1Ynj Numbltm1Wmz/Numbltm1Wmz
(involves: 129S2/SvPas * 129X1/SvJ * CD-1)
|
abnormal neuron differentiation
|
J:87149
|
increased neuron apoptosis
|
J:87149
|
Emx1tm1(cre)Krj/Emx1+ Rbm8atm1Dlsi/Rbm8a+
(involves: C57BL/6J)
|
abnormal radial glial cell apoptosis
|
J:221648
|
abnormal radial glial cell morphology
|
J:221648
|
decreased radial glial cell number
|
J:221648
|
impaired neuron differentiation
|
J:221648
|
increased forebrain apoptosis
|
J:221648
|
increased neuron apoptosis
|
J:221648
|
increased neuronal precursor proliferation
|
J:221648
|
premature neuronal precursor differentiation
|
J:221648
|
Emx1tm1(cre)Krj/Emx1+ Snord118em1Jfch/Snord118+
(B6.Cg-Emx1tm1(cre)Krj Snord118em1Jfch)
|
abnormal cell physiology
|
J:344970
|
decreased neuronal precursor proliferation
|
J:344970
|
Emx1tm1(cre)Krj/Emx1+ Snord118em1Jfch/Snord118em1Jfch
(B6.Cg-Emx1tm1(cre)Krj Snord118em1Jfch)
|
abnormal cell physiology
|
J:344970
|
decreased neuronal precursor proliferation
|
J:344970
|
increased neuron apoptosis
|
J:344970
|
Emx1tm1(cre)Krj/Emx1+ Tg(CMV-GFP,-Smarcc2,-lacZ)#Stoy/0
(involves: 129S2/SvPas)
|
abnormal DNA methylation
|
J:197141
|
abnormal neuron differentiation
|
J:197141
|
Emx2tm1Sia/Emx2tm1Sia
(involves: C57BL/6 * CBA)
|
increased metanephric mesenchyme apoptosis
|
J:40605
|
Emx2wndr/Emx2wndr Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw
(involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal axon extension
|
J:168258
|
En1tm1(PDGFB)Nist/En1+
(involves: 129/Sv * C57BL/6)
|
abnormal cell migration
|
J:90898
|
En1tm1(Wnt1)Wrst/En1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell cycle
|
J:91004
|
increased cell proliferation
|
J:91004
|
En1tm1Alj/En1tm8.1Alj En2tm1Alj/En2tm6Alj Gt(ROSA)26Sortm1(cre/ERT2)Alj/Gt(ROSA)26Sor+
(involves: 129S2/SvPas * 129S6/SvEvTac * Swiss Webster)
|
abnormal cerebellar granule cell precursor proliferation
|
J:156169
|
En1tm1Gld/En1+ Ntn1Gt(ST629)Byg/Ntn1Gt(ST629)Byg
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6)
|
abnormal axon extension
|
J:52637
|
abnormal axon guidance
|
J:52637
|
En1tm1Gld/En1tm1Gld
(involves: 129S/SvEv * C57BL/6)
|
abnormal axon guidance
|
J:52637
|
abnormal neuron differentiation
|
J:52637
|
En1tm2(cre)Wrst/En1+ Gata2tm1Msal/Gata2tm1Msal
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:143527
|
En1tm2(cre)Wrst/En1+ Mfn2tm1Dcc/Mfn2tm3Dcc
(involves: 129 * 129S4/SvJaeSor * Black Swiss)
|
abnormal neuron mitochondrial morphology
|
J:132329
|
increased neuron apoptosis
|
J:132329
|
En1tm2Alj/En1+ Tg(Th-EGFP)6-7Okn/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2J * OF1)
|
abnormal autophagy
|
J:214073
|
Enahtm1Fbg/Enahtm1Fbg
(involves: 129S4/SvJaeSor)
|
abnormal axon guidance
|
J:53259
|
Enahtm1Fbg/Enahtm1Fbg Evltm1Fbg/Evltm1Fbg Vasptm1Ref/Vasptm1Ref
(involves: 129 * BALB/c * C57BL/6)
|
abnormal radial glial cell morphology
|
J:127447
|
Enahtm2.1Fbg/Enahtm2.1Fbg Vasptm1Ref/Vasptm1Ref
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
abnormal cell adhesion
|
J:190748
|
Endog/D2Wsu81etm1Mxu/Endog+
(involves: 129 * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:88144
|
decreased sensitivity to induced cell death
|
J:88144
|
Endoutm1Tft/Endoutm1Tft Tg(IghelMD4)4Ccg/0 Tg(ML5sHEL)5Ccg/0
(involves: 129S/SvEv * C57BL/6 * C57BL/6JSfd)
|
decreased activation-induced B cell apoptosis
|
J:208364
|
Engasetm1Tasuz/Engasetm1Tasuz Ngly1tm1.1Tasuz/Ngly1tm1.1Tasuz
(B6.Cg-Engasetm1Tasuz Ngly1tm1.1Tasuz)
|
cellular phenotype
|
J:217663
|
Enhotm1.1Butl/Enhotm1.1Butl
(B6.Cg-Enhotm1.1Butl)
|
decreased skeletal muscle cell glucose uptake
|
J:225402
|
Enkd1em1Jzho/Enkd1em1Jzho
(C57BL/6J-Enkd1em1Jzho)
|
abnormal cilium morphology
|
J:326906
|
abnormal kidney epithelial cell primary cilium morphology
|
J:326906
|
abnormal photoreceptor connecting cilium morphology
|
J:326906
|
absent sperm flagellum
|
J:326906
|
Enkurtm1Hmf/Enkurtm1Hmf
(involves: 129 * C57BL/6J)
|
abnormal sperm motility
|
J:266551
|
decreased sperm progressive motility
|
J:266551
|
impaired sperm migration in female genital tract
|
J:266551
|
Eno2tm1(DTA)Hsak/Eno2+ Gng7tm2(cre/PGR)Mmsh/Gng7+
(involves: C57BL/6)
|
increased neuron apoptosis
|
J:145152
|
Eno4Gt(RRF299)Byg/Eno4Gt(RRF299)Byg
(either: (involves: 129P2/OlaHsd * 129S6/SvEvTac) or (involves: 129P2/OlaHsd * C57BL/6))
|
abnormal sperm annulus morphology
|
J:202075
|
abnormal sperm axoneme morphology
|
J:202075
|
abnormal sperm end piece morphology
|
J:202075
|
abnormal sperm fibrous sheath morphology
|
J:202075
|
abnormal sperm flagellum morphology
|
J:202075
|
abnormal sperm midpiece morphology
|
J:202075
|
abnormal sperm principal piece morphology
|
J:202075
|
absent sperm annulus
|
J:202075
|
asthenozoospermia
|
J:202075
|
kinked sperm flagellum
|
J:202075
|
oligozoospermia
|
J:202075
|
Enpp1asj/Enpp1asj
(C57BL/6J-Enpp1asj/GrsrJ)
|
increased middle ear goblet cell number
|
J:251638
|
Enpp1tm1Gdg/Enpp1tm1Gdg
(involves: 129S1/Sv)
|
abnormal osteoblast physiology
|
J:111462
|
Enpp1ttw/Enpp1ttw
(involves: ICR)
|
abnormal chondrocyte proliferation
|
J:37369
|
Enpp2tm1.1Vart/Enpp2tm1.1Vart
(B6.Cg-Enpp2tm1.1Vart/Flmg)
|
abnormal axon extension
|
J:159118
|
decreased cell proliferation
|
J:159118
|
increased neural tube apoptosis
|
J:159118
|
Entpd5tm1Rre/Entpd5tm1Rre
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:163795
|
increased hepatocyte apoptosis
|
J:163795
|
increased hepatocyte proliferation
|
J:163795
|
Entpd8tm1Ktak/Entpd8tm1Ktak
(C.Cg-Entpd8tm1Ktak)
|
decreased apoptosis
|
J:311564
|
Eomestm1.1Bflu/Eomestm1.1Bflu Tbx21tm1Glm/Tbx21tm1Glm Tg(Cd4-cre)1Cwi/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2 * SJL)
|
abnormal leukocyte migration
|
J:163822
|
Eomestm1.1Bflu/Eomestm1.1Bflu Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * DBA/2 * SJL)
|
abnormal leukocyte migration
|
J:163822
|
Eomestm1.1Rob/Eomes+ Nodaltm1Rob/Nodal+
(involves: 129S/SvEv * 129S7/SvEvBrd * C57BL/6 * CBA)
|
abnormal anterior visceral endoderm cell migration
|
J:131055
|
Eomestm1.1Whk/Eomestm1.1Whk Tg(Six3-cre)69Frty/0
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased retina apoptosis
|
J:130570
|
Eomestm1Rob/Eomestm1Rob Sox1tm1(cre)Take/0
(involves: 129S/SvEv * C57BL/6 * CBA)
|
abnormal axon guidance
|
J:138764
|
abnormal neuron apoptosis
|
J:138764
|
abnormal neuronal precursor proliferation
|
J:138764
|
Ep300tm1Dli/Ep300tm1Dli
(either: 129S4/SvJae or (involves: 129S4/SvJae * C57BL/6))
|
abnormal cell physiology
|
J:47301
|
decreased fibroblast proliferation
|
J:47301
|
early cellular replicative senescence
|
J:47301
|
Epb41l2Gt(AL0682)Wtsi/Epb41l2Gt(AL0682)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
oligozoospermia
|
J:173777
|
Epb41l3tm1Jkis/Epb41l3tm1Jkis
(involves: 129S4/SvJae)
|
cellular phenotype
|
J:102380
|
Epb41l5lulu/Epb41l5lulu
(involves: C57BL/6J)
|
abnormal cell nucleus morphology
|
J:122548
|
Epcamtm1.1Mcu/Epcamtm1.1Mcu Tg(CD207-cre)1Dhka/0
(involves: 129 * C57BL/6 * C57BL/6J * SJL/J)
|
abnormal cell migration
|
J:182665
|
Epcamtm1.2Msiv/Epcamtm1.2Msiv
(involves: C57BL/6 * FVB/N * SJL)
|
abnormal enterocyte proliferation
|
J:210901
|
Epg5tm1Ygz/Epg5tm1Ygz
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)
|
abnormal autophagy
|
J:196603
|
impaired autophagy
|
J:279837
|
increased mitochondrial size
|
J:196603
|
increased retina apoptosis
|
J:279837
|
Epha4Gt(PST038)Byg/Epha4Gt(PST038)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal axon guidance
|
J:70273,
J:67920
|
Epha4Gt(PST038)Byg/Epha4Gt(PST038)Byg Rettm1.1Kln/Rettm1.1Kln
(involves: 129/Sv * BALB/c * C57BL/6 * CBA/J)
|
abnormal axon guidance
|
J:110955
|
Epha4tm1.2Bzh/Epha4tm1.2Bzh Tg(Hlxb9-GFP)1Tmj/0
(involves: 129S/Sv * C57BL/6J * CD-1 * FVB/N)
|
abnormal axon fasciculation
|
J:243785
|
Epha8tm1Bbd/Epha8tm1Bbd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal axon guidance
|
J:41127
|
Ephb1tm1.1Meg/Ephb1tm1.1Meg Ephb2tm1.1Meg/Ephb2tm1.1Meg Ephb3tm1.1Meg/Ephb3tm1.1Meg
(involves: 129S4/SvJae * C57BL/6)
|
abnormal axon extension
|
J:197489
|
Ephb1tm1Cmn/Ephb1tm1Cmn
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon pruning
|
J:150550
|
Ephb1tm1Cmn/Ephb1tm1Cmn Ephb2tm1Paw/Ephb2tm1Paw
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon pruning
|
J:150550
|
Ephb1tm1Cmn/Ephb1tm1Cmn Ephb2tm1Paw/Ephb2tm1Paw Ephb3tm1Kln/Ephb3tm1Kln
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon pruning
|
J:150550
|
Ephb1tm1Dgen/Ephb1+ Fezf2tm1Skm/Fezf2tm1Skm
(involves: 129)
|
abnormal axon guidance
|
J:214959
|
Ephb1tm1Dgen/Ephb1tm1Dgen
(Not Specified)
|
abnormal axon fasciculation
|
J:214959
|
abnormal axon guidance
|
J:214959
|
Ephb1tm1Dgen/Ephb1tm1Dgen Fezf2tm1Skm/Fezf2+
(involves: 129)
|
abnormal axon guidance
|
J:214959
|
Ephb2tm1Paw/Ephb2tm1Paw
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon guidance
|
J:62565
|
abnormal axon pruning
|
J:150550
|
delayed axon extension
|
J:62565
|
Ephb2tm1Paw/Ephb2tm1Paw
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
abnormal axon guidance
|
J:34200
|
Ephb2tm1Paw/Ephb2tm1Paw Ephb3tm1Kln/Ephb3tm1Kln
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon guidance
|
J:62565
|
delayed axon extension
|
J:62565
|
Ephb2tm2Paw/Ephb2tm2Paw
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon guidance
|
J:62565
|
delayed axon extension
|
J:62565
|
Ephb2tm2Paw/Ephb2tm2Paw Ephb3tm1Kln/Ephb3tm1Kln
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon guidance
|
J:62565
|
delayed axon extension
|
J:62565
|
Ephb2tm3.1Jf/Ephb2tm3.1Jf Ephb3tm1Kln/Ephb3tm1Kln
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * CD-1)
|
abnormal small intestinal crypt cell proliferation
|
J:157019
|
Ephb3tm1Kln/Ephb3tm1Kln
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon pruning
|
J:150550
|
Ephb6/Trpv6tm1.1Mfre/Ephb6/Trpv6tm1.1Mfre
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N)
|
asthenozoospermia
|
J:185996
|
necrospermia
|
J:185996
|
Ephb6/Trpv6tm1.1Mfre/Ephb6/Trpv6tm1.1Mfre
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N)
|
asthenozoospermia
|
J:185996
|
necrospermia
|
J:185996
|
Ephb6tm1Jwu/Ephb6tm1Jwu
(involves: 129)
|
decreased T cell proliferation
|
J:94701
|
epi/?
(involves: CBA/J)
|
abnormal autophagy
|
J:5752
|
Epm2aTg(TcraK,TcrbK)TG-BFlv/Epm2a+
(involves: C57BL/6 * C57BL/10 * C57BR/cd * CBA/J)
|
abnormal DNA methylation
|
J:112696
|
Epm2atm1Kzy/Epm2atm1Kzy
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased cardiac muscle cell glucose uptake
|
J:173769
|
increased neuron apoptosis
|
J:76688
|
Epn1tm1.1Wami/Epn1tm1.1Wami Epn2tm1Ocr/Epn2tm1Ocr Tg(Cdh5-cre/ERT2)CIVE23Mlia/0
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal vascular endothelial cell migration
|
J:193966
|
increased vascular endothelial cell proliferation
|
J:193966
|
Epn1tm1Ocr/Epn1tm1Ocr Epn2tm1Ocr/Epn2tm1Ocr
(B6.129X1-Epn1tm1Ocr Epn2tm1Ocr)
|
cellular phenotype
|
J:151951
|
Epotm1Jae/Epotm1Jae
(either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6))
|
increased hepatocyte apoptosis
|
J:29254
|
Eportm1Jae/Eportm1Jae
(either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6))
|
increased hepatocyte apoptosis
|
J:29254
|
Eportm1Lizon/Eportm1Lizon
(involves: 129S4/SvJae * C57BL/6)
|
increased hepatocyte apoptosis
|
J:35594
|
Eportm1Lizon/Eportm1Lizon Tg(Gata1-Epor)AMym/0
(involves: 129S4/SvJae * C57BL/6 * DBA)
|
abnormal vascular endothelial cell migration
|
J:121500
|
Eppk1tm1Safu/Eppk1tm1Safu
(involves: 129 * C57BL/6J)
|
increased keratinocyte migration
|
J:144147
|
Eprs1tm1.1Xen/Eprs1tm1.1Xen
(C57BL/6-Eprs1tm1.1Xen)
|
increased fatty acid beta-oxidation
|
J:244749
|
Eps8tm1Ppdf/Eps8tm1Ppdf
(B6.129P2-Eps8tm1Ppdf)
|
abnormal cell physiology
|
J:116055
|
Eps15tm1c(KOMP)Wtsi/Eps15tm1c(KOMP)Wtsi Eps15l1tm2.1Noff/Eps15l1tm2.1Noff Tg(Tek-cre)1Ywa/0
(involves: C57BL/6 * C57BL/6N * SJL)
|
abnormal endocytosis
|
J:272122
|
Eps15l1tm1.1Noff/Eps15l1tm1.1Noff
(B6(Cg)-Eps15l1tm1.1Noff)
|
abnormal endocytosis
|
J:272122
|
Epsti1em1Mjnh/Epsti1em1Mjnh
(Not Specified)
|
abnormal macrophage differentiation
|
J:272013
|
Eqtntm1Gar/Eqtntm1Gar
(involves: 129 * C57BL/6)
|
oligozoospermia
|
J:219150
|
Erap1tm1.1Gnie/Erap1tm1.1Gnie
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased T cell proliferation
|
J:143988
|
Erbb2tm1Cbm/Erbb2tm1Cbm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neural crest cell migration
|
J:48515
|
Erbb2tm3(Erbb2)Mul/Erbb2tm3(Erbb2)Mul Tg(Ckmm-cre)5Khn/0
(involves: 129S1/Sv * 129X1/SvJ * BALB/c * FVB)
|
increased myoblast apoptosis
|
J:81565
|
Erbb2tm4(Erbb2)Mul/Erbb2tm1Haus
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c)
|
defasiculated phrenic nerve
|
J:94397
|
Erbb2tm6(Erbb2)Mul/Erbb2tm1Haus
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c)
|
defasiculated phrenic nerve
|
J:94397
|
Erbb2tm7(Erbb2)Mul/Erbb2tm1Haus
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * BALB/c)
|
defasiculated phrenic nerve
|
J:94397
|
Erbb3m3329Ddg/Erbb3m3329Ddg
(involves: C57BL/6)
|
abnormal axon fasciculation
|
J:160880
|
Erbb3m3329Ddg/Erbb3m3329Ddg
(involves: C3H/He * C57BL/6)
|
abnormal axon fasciculation
|
J:159834
|
Erbb3m3329Ddg/Erbb3tm1Gne
(involves: 129S2/SvPas * C57BL/6)
|
abnormal axon fasciculation
|
J:160880
|
Erbb3tm1Cbm/Erbb3tm1Cbm
(either: 129P2/OlaHsd or (involves: 129P2/OlaHsd * C57BL/6))
|
increased neuron apoptosis
|
J:43515
|
Erbb3tm1Gne/Erbb3tm1Gne
(involves: 129S2/SvPas * C57BL/6)
|
impaired neuronal migration
|
J:45302
|
Erbb3tm2Cbm/Erbb3tm2Cbm
(either: 129P2/OlaHsd or (involves: 129P2/OlaHsd * C57BL/6))
|
increased neuron apoptosis
|
J:43515
|
Erbb3tm2Cbm/Erbb3tm2Cbm
(involves: 129P2/OlaHsd)
|
abnormal neural crest cell migration
|
J:48515
|
Erbb4tm1Grl/Erbb4tm1Grl Tg(Myh6-ERBB4)HT2Gass/0
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cranial neural crest cell migration
|
J:84403
|
Ercc1tm1Dwm/Ercc1tm1Dwm
(involves: 129P2/OlaHsd * BALB/c)
|
abnormal cell nucleus morphology
|
J:15422
|
aneuploidy
|
J:15422
|
polyploidy
|
J:15422
|
Ercc1tm1Dwm/Ercc1tm1Dwm Tg(Ttr-Ercc1)17Dwm/0
(involves: 129P2/OlaHsd * BALB/c)
|
abnormal chromosome number
|
J:106084
|
abnormal male germ cell apoptosis
|
J:80586
|
decreased germ cell number
|
J:80586
|
polyploidy
|
J:106084
|
Ercc1tm1Jhjh/Ercc1tm1Jhjh
(involves: C57BL/6 * FVB/N)
|
decreased B cell proliferation
|
J:92471
|
Ercc1tm1Jhjh/Ercc1tm1Jhjh
(involves: 129P2/OlaHsd * C57BL/6 * FVB)
|
abnormal DNA repair
|
J:117488
|
decreased cell proliferation
|
J:117488
|
decreased hepatocyte proliferation
|
J:117488
|
early cellular replicative senescence
|
J:117488
|
increased cellular sensitivity to oxidative stress
|
J:117488
|
increased hepatocyte apoptosis
|
J:117488
|
Ercc1tm1Jhjh/Ercc1tm2Jhjh
(involves: 129P2/OlaHsd * C57BL/6J * FVB/N)
|
increased retina apoptosis
|
J:280844
|
Ercc1tm2Jhjh/Ercc1tm2Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cell proliferation
|
J:41161
|
Ercc2tm1Jhjh/Ercc2tm2(ERCC2)Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:116054
|
Ercc2tm1Jmch/Ercc2tm2(ERCC2)Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:116054
|
Ercc2tm2(ERCC2)Jhjh/Ercc2tm2(ERCC2)Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:112689
|
Ercc2tm2(ERCC2)Jhjh/Ercc2tm2(ERCC2)Jhjh
(involves: 129P2/OlaHsd)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:145759
|
Ercc2tm2(ERCC2)Jhjh/Ercc2tm2(ERCC2)Jhjh Ercc3tm2Jhjh/Ercc3tm2Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:145759
|
increased cellular sensitivity to oxidative stress
|
J:145759
|
increased cellular sensitivity to ultraviolet irradiation
|
J:145759
|
Ercc2tm2(ERCC2)Jhjh/Ercc2tm2(ERCC2)Jhjh Xpatm1Hvs/Xpatm1Hvs
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell death
|
J:76608
|
increased cellular sensitivity to oxidative stress
|
J:76608
|
increased cellular sensitivity to ultraviolet irradiation
|
J:76608
|
increased cellular sensitivity to X-ray irradiation
|
J:76608
|
Ercc2tm2(ERCC2)Jhjh/Ercc2tm2Jmch
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:116054
|
Ercc2tm3Jhjh/Ercc2tm3Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:116054
|
Ercc2tm3Jhjh/Ercc2tm3Jhjh
(involves: 129P2/OlaHsd * C57BL/6 * FVB)
|
abnormal DNA repair
|
J:112689
|
increased cellular sensitivity to ultraviolet irradiation
|
J:112689
|
Ercc3tm1.1Gima/Ercc3tm1.1Gima
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB))
|
cellular phenotype
|
J:154596
|
Ercc3tm1.1Gima/Ercc3tm1.1Gima Xpctm1Ecf/Xpctm1Ecf
(either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129P2/OlaHsd * FVB/N))
|
increased cellular sensitivity to ultraviolet irradiation
|
J:154596
|
Ercc3tm2Jhjh/Ercc3tm2Jhjh
(B6.129P2-Ercc3tm2Jhjh)
|
increased cellular sensitivity to gamma-irradiation
|
J:145759
|
increased cellular sensitivity to ultraviolet irradiation
|
J:145759
|
Ercc3tm2Jhjh/Ercc3tm2Jhjh Xpatm1Hvs/Xpatm1Hvs
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:145759
|
increased cellular sensitivity to oxidative stress
|
J:145759
|
increased cellular sensitivity to ultraviolet irradiation
|
J:145759
|
Ercc4tm1Fwa/Ercc4tm1Fwa
(involves: 129S6/SvEvTac)
|
abnormal DNA repair
|
J:87684
|
cellular phenotype
|
J:87684
|
increased cellular sensitivity to alkylating agents
|
J:87684
|
increased cellular sensitivity to ultraviolet irradiation
|
J:87684
|
increased hepatocyte karyomegaly
|
J:87684
|
Ercc4tm1Fwa/Ercc4tm1Fwa
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
cellular phenotype
|
J:102653
|
Ercc4tm1Fwa/Ercc4tm1Fwa Tg(KRT5-Terf2)PMBlas/Y
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal telomere morphology
|
J:102653
|
Ercc6tm1Gvh/Ercc6tm1Gvh
(involves: 129P2/OlaHsd * FVB)
|
abnormal cell physiology
|
J:40211
|
increased cellular sensitivity to ultraviolet irradiation
|
J:40211
|
Ercc6tm1Gvh/Ercc6tm1Gvh
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:122013
|
Ercc6tm1Gvh/Ercc6tm1Gvh Xpatm1Hvs/Xpatm1Hvs
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal base-excision repair
|
J:122013
|
increased cellular sensitivity to ultraviolet irradiation
|
J:122013
|
Ercc6tm1Gvh/Ercc6tm1Gvh Xpatm1Hvs/Xpatm1Hvs
(B6.129P2-Xpatm1Hvs Ercc6tm1Gvh)
|
increased cellular sensitivity to gamma-irradiation
|
J:122013
|
Ercc6tm1Gvh/Ercc6tm1Gvh Xpatm1Tnka/Xpatm1Tnka
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased cerebellar granule cell precursor proliferation
|
J:72574
|
Ercc6tm1Gvh/Ercc6tm1Gvh Xpctm1Ecf/Xpctm1Ecf
(involves: 129 * 129P2/OlaHsd * C57BL/6J)
|
abnormal base-excision repair
|
J:122013
|
increased cellular sensitivity to ultraviolet irradiation
|
J:122013
|
Ercc6ltm1.2Ajlc/Y
(involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J)
|
abnormal cell cycle checkpoint function
|
J:271028
|
abnormal cell nucleus morphology
|
J:271028
|
abnormal cell physiology
|
J:271028
|
abnormal DNA replication
|
J:271028
|
chromosomal instability
|
J:271028
|
decreased fibroblast proliferation
|
J:271028
|
early cellular replicative senescence
|
J:271028
|
increased brain apoptosis
|
J:271028
|
increased embryonic tissue cell apoptosis
|
J:271028
|
polyploidy
|
J:271028
|
Ercc6ltm1.2Ajlc/Y Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J)
|
chromosomal instability
|
J:271028
|
increased embryonic tissue cell apoptosis
|
J:271028
|
Ercc6ltm1.2Ajlc/Y Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J)
|
chromosomal instability
|
J:271028
|
increased embryonic tissue cell apoptosis
|
J:271028
|
Ercc6ltm1.2Ajlc/Ercc6l+
(involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL/J)
|
abnormal cell nucleus morphology
|
J:271028
|
abnormal cell physiology
|
J:271028
|
chromosomal instability
|
J:271028
|
decreased fibroblast proliferation
|
J:271028
|
Ercc8tm1Jhjh/Ercc8tm1Jhjh
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal DNA repair
|
J:74959
|
increased cellular sensitivity to ultraviolet irradiation
|
J:74959
|
Erftm1Gmav/Erftm1Gmav
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
increased apoptosis
|
J:123628
|
Ergtm1.1Path/Ergtm1.1Path
(Not Specified)
|
increased vascular endothelial cell proliferation
|
J:227456
|
Eri1tm1.2Anse/Eri1tm1.2Anse
(involves: BALB/cJ * C57BL/6 * SJL)
|
decreased cell proliferation
|
J:146701
|
Ern1tm1Rjk/Ern1tm1Rjk
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:124971
|
Ern1tm1Rjk/Ern1tm2.1Rjk Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA)
|
increased hepatocyte apoptosis
|
J:171230
|
Ero1aGt(XST171)Byg/Ero1aGt(XST171)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased macrophage apoptosis
|
J:153833
|
decreased sensitivity to induced cell death
|
J:153833
|
Erp29tm1Dfer/Erp29tm1Dfer
(involves: 129S2/SvPas * C57BL/6N)
|
decreased cellular sensitivity to hydrogen peroxide
|
J:217253
|
decreased sensitivity to induced cell death
|
J:217253
|
Esamtm1Dvst/Esamtm1Dvst
(B6.129-Esam1tm1Dvst)
|
abnormal cellular extravasation
|
J:124397
|
abnormal leukocyte migration
|
J:124397
|
Esco1tm1.1Ge/Esco1tm1.1Ge Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal mitosis
|
J:296958
|
Esco2tm1.1Ge/Esco2tm1.1Ge Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal mitosis
|
J:296958
|
Esco2tm1.1Ge/Esco2tm1.1Ge Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S2/SvPas * C57BL/6 * CBA * SJL)
|
abnormal cell nucleus morphology
|
J:180371
|
abnormal chromosome morphology
|
J:180371
|
abnormal mitosis
|
J:180371
|
decreased cell proliferation
|
J:180371
|
increased mitotic index
|
J:180371
|
Esco2tm1.2Ge/Esco2tm1.2Ge
(involves: 129S2/SvPas * C57BL/6 * FVB/N * SJL)
|
abnormal mitosis
|
J:180371
|
Esm1tm1.1Rha/Esm1tm1.1Rha
(involves: 129S6/SvEvTac * BALB/c * C57BL/6 * C57BL/6NTac)
|
abnormal cellular extravasation
|
J:246778
|
Espl1Gt(XL058)Byg/Espl1+ Trp53tm1Tyj/Trp53tm1Tyj
(B6.129-Trp53tm1Tyj Espl1Gt(XL058)Byg)
|
aneuploidy
|
J:174926
|
increased splenocyte proliferation
|
J:174926
|
Espl1tm1.1Kna/Espl1tm1.2Kna Wapltm1.1Jmpt/Wapltm1.2Jmpt Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NTac * SJL)
|
abnormal mitosis
|
J:205429
|
Espl1tm1.1Tno/Espl1+
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal chromosome morphology
|
J:107917
|
Espl1tm1.1Tno/Espl1+ Pttg1tm1.1Tno/Pttg1tm1.1Tno
(involves: 129S4/SvJae * C57BL/6J)
|
decreased cell proliferation
|
J:107917
|
Espl1tm1.1Tno/Espl1tm1.2Tno
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:107917
|
decreased cell proliferation
|
J:107917
|
Espl1tm1.2Kna/Espl1+ Pttg1tm1.2Kna/Pttg1tm1.2Kna
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell death
|
J:107916
|
abnormal cell nucleus morphology
|
J:107916
|
abnormal mitosis
|
J:107916
|
abnormal mitotic spindle morphology
|
J:107916
|
Espl1tm1.2Tno/Espl1tm1.2Tno
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:107917
|
abnormal inner cell mass proliferation
|
J:107917
|
Espl1tm2Pzg/Espl1+ Meox2tm1(cre)Sor/Meox2+
(involves: 129S4/SvJaeSor * 129S7/SvEvBrd)
|
abnormal centrosome morphology
|
J:131838
|
abnormal male germ cell morphology
|
J:131838
|
abnormal mitosis
|
J:131838
|
abnormal spermatocyte morphology
|
J:131838
|
absent primordial germ cells
|
J:131838
|
absent spermatogonia
|
J:131838
|
aneuploidy
|
J:131838
|
decreased primordial germ cell proliferation
|
J:131838
|
decreased spermatid number
|
J:131838
|
increased mitotic index
|
J:131838
|
Espnje/? f/f Hps6ru/Hps6ru
(JE/LeJ)
|
abnormal mast cell degranulation
|
J:37255
|
Esr1tm1.1Ics/Esr1tm1.1Ics
(involves: C57BL/6NTac)
|
abnormal cell migration
|
J:206373
|
Esr1tm1.1Mma/Esr1+ Esr2tm1Mma/Esr2tm1Mma
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
impaired granulosa cell differentiation
|
J:64426
|
Esr1tm1.1Mma/Esr1tm1.1Mma
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
decreased male germ cell number
|
J:64426
|
Esr1tm1.1Mma/Esr1tm1.1Mma Esr2tm1Mma/Esr2tm1Mma
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
decreased male germ cell number
|
J:64426
|
impaired granulosa cell differentiation
|
J:64426
|
Esr1tm1.2Mma/Esr1tm1.2Mma Tg(Cyp17a1-icre)AJako/0
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
oocyte degeneration
|
J:151908
|
Esr1tm1Geog/Esr1tm1Geog
(involves: 129X1/SvJ * C57BL/6)
|
impaired granulosa cell differentiation
|
J:135981
|
Esr1tm1Ksk/Esr1tm1Ksk
(involves: 129P2/OlaHsd * C57BL/6J)
|
asthenozoospermia
|
J:36658
|
detached sperm flagellum
|
J:36658
|
oligozoospermia
|
J:16338,
J:36658
|
teratozoospermia
|
J:36658
|
Esr1tm1Ksk/Esr1tm1Ksk
(involves: 129P2/OlaHsd)
|
oligozoospermia
|
J:60490
|
Esr1tm1Ksk/Esr1tm1Ksk
(B6.129P2-Esr1tm1Ksk/J)
|
oligozoospermia
|
J:147000
|
Esr1tm1Ksk/Esr1tm1Ksk Esr2tm1Unc/Esr2tm1Unc
(involves: 129P2/OlaHsd)
|
asthenozoospermia
|
J:59105
|
oligozoospermia
|
J:59105
|
Esr1tm1Ksk/Esr1tm1Ksk Esr2tm1Unc/Esr2tm1Unc Inhatm1Bay/Inhatm1Bay
(involves: 129P2/OlaHsd * 129S6/SvEvTac * 129S7/SvEvBrd)
|
decreased male germ cell number
|
J:84989
|
Esr1tm1Syeh/Esr1tm1Syeh Tmem163Tg(ACTB-cre)2Mrt/0
(involves: 129X1/SvJ * FVB/N)
|
decreased male germ cell number
|
J:147000
|
oligozoospermia
|
J:147000
|
Esr1tm4.2Ksk/Esr1tm4.2Ksk Mir22tm1Boet/Mir22tm1Boet Tg(Ckmm-cre)5Khn/0
(involves: 129S2/SvPas * C57BL/6 * FVB)
|
increased fatty acid oxidation
|
J:266382
|
Esr2tm1Mma/Esr2+
(involves: 129S2/SvPas)
|
abnormal germ cell morphology
|
J:105626
|
Esr2tm1Mma/Esr2tm1Mma
(involves: 129S2/SvPas)
|
abnormal germ cell morphology
|
J:105626
|
Esr2tm1Unc/Esr2tm1Unc
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased keratinocyte apoptosis
|
J:107589
|
Esr2tm1Unc/Esr2tm1Unc
(involves: 129P2/OlaHsd)
|
abnormal enterocyte proliferation
|
J:107308
|
decreased enterocyte apoptosis
|
J:107308
|
Esrp2tm1(KOMP)Vlcg/Esrp2tm1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
increased hepatocyte proliferation
|
J:228040
|
Esrratm1Vgi/Esrratm1Vgi
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cellular respiration
|
J:119525
|
decreased fat cell mitochondrial DNA content
|
J:119525
|
decreased mitochondrial number
|
J:119525
|
Esrratm1Vgi/Esrratm1Vgi
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoclast differentiation
|
J:160910
|
Esrrgtm1Rev/Esrrg+
(either: (involves: 129) or (involves: C57BL/6) or (involves: ICR))
|
increased mitochondrial number
|
J:129851
|
Esrrgtm1Rev/Esrrgtm1Rev
(either: (involves: 129) or (involves: C57BL/6) or (involves: ICR))
|
abnormal respiratory electron transport chain
|
J:129851
|
increased mitochondrial number
|
J:129851
|
Esyt2Gt(AN0678)Wtsi/Esyt2Gt(AN0678)Wtsi
(involves: 129P2/OlaHsd)
|
decreased cell migration
|
J:232605
|
Esyt2Gt(AN0678)Wtsi/Esyt2Gt(AN0678)Wtsi Esyt3tm1d(EUCOMM)Wtsi/Esyt3tm1d(EUCOMM)Wtsi
(involves: 129P2/OlaHsd * C57BL/6N)
|
decreased cell migration
|
J:232605
|
increased cellular sensitivity to oxidative stress
|
J:232605
|
increased sensitivity to induced cell death
|
J:232605
|
Etfbkmtem1Yshk/Etfbkmtem1Yshk
(C57BL/6J-Etfbkmtem1Yshk)
|
abnormal mitochondrial physiology
|
J:260200
|
increased fatty acid beta-oxidation
|
J:260200
|
Etfdhtm1c(EUCOMM)Hmgu/Etfdhtm1c(EUCOMM)Hmgu Tg(ACTA1-rtTA,tetO-cre)102Monk/0
(involves: C3H * C57BL/6 * C57BL/6N)
|
abnormal oxidative phosphorylation
|
J:345923
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:345923
|
disorganized mitochondrial cristae
|
J:345923
|
increased skeletal muscle fiber mitochondrial size
|
J:345923
|
Etnk2tm1Mkar/Etnk2tm1Mkar
(involves: 129S7/SvEvBrd * C57BL/6J)
|
maternal effect
|
J:117170
|
Ets1tm1.1Dds/Ets1+
(129S6/SvEvTac-Ets1tm1.1Dds)
|
decreased thymocyte apoptosis
|
J:121460
|
increased splenocyte apoptosis
|
J:121460
|
Ets1tm1.1Dds/Ets1tm1.1Dds
(129S6/SvEvTac-Ets1tm1.1Dds)
|
decreased thymocyte apoptosis
|
J:121460
|
increased cell proliferation
|
J:121460
|
increased splenocyte apoptosis
|
J:121460
|
Ets1tm1Fwa/Ets1tm1Fwa
(B6.129S4-Ets1tm1Fwa)
|
decreased B cell proliferation
|
J:93845
|
increased B cell apoptosis
|
J:93845
|
Ets1tm1Jml/Ets1tm1Jml Ets2tm2Rgo/Ets2tm2Rgo
(involves: 129S/SvEv * C57BL/6 * FVB/N)
|
increased vascular endothelial cell apoptosis
|
J:151187
|
Ets1tm1Jml/Ets1tm1Jml Ets2tm5.1Rgo/Ets2tm5.1Rgo Tg(Tek-cre)1Ywa/0
(involves: 129S/SvEv * C57BL/6 * FVB/N)
|
increased vascular endothelial cell apoptosis
|
J:151187
|
Ets1tm2Jml/Ets1tm2Jml
(involves: 129X1/SvJ * C57BL/6)
|
decreased T cell proliferation
|
J:50627
|
Ets1tm2Jml/Ets1tm2Jml Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ Pax3tm1(cre)Joe/Pax3+
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6J * C57BL/6NCrl)
|
abnormal cardiac neural crest cell migration
|
J:334073
|
abnormal neural crest cell physiology
|
J:334073
|
Etv1tm2Tmj/Etv1tm2Tmj Tg(Ntrk3-EGFP)BM45Gsat/0
(involves: 129S1/Sv * FVB/N)
|
abnormal axon guidance
|
J:197913
|
Etv2tm1Dlim/Etv2tm1Dlim
(involves: C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:155850
|
Etv5sco/Etv5sco
(involves: C57BL/6JAnu * CBA)
|
azoospermia
|
J:208684
|
decreased male germ cell number
|
J:208684
|
Etv5tm1Kmm/Etv5tm1Kmm
(involves: 129S6/SvEvTac)
|
abnormal spermatocyte morphology
|
J:100645
|
abnormal spermatogonia proliferation
|
J:100645
|
absent spermatogonia
|
J:135433
|
asthenozoospermia
|
J:135433
|
azoospermia
|
J:100645
|
decreased spermatogonia number
|
J:135433,
J:100645
|
increased male germ cell apoptosis
|
J:135433
|
oligozoospermia
|
J:135433
|
Etv6tm2Sho/Etv6tm2Sho Tg(Gata1-cre)1Sho/?
(involves: 129S1/Sv)
|
abnormal megakaryocyte differentiation
|
J:93052
|
Eva1atm1Nju/Eva1atm1Nju Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
impaired autophagy
|
J:301660
|
Evc2tm1.1Vlrp/Evc2tm1.1Vlrp
(involves: 129 * C57BL/6J)
|
impaired osteoblast differentiation
|
J:188176
|
Evctm1Jago/Evctm1Jago Evc2tm1.1Vlrp/Evc2tm1.1Vlrp
(involves: 129 * 129S7/SvEvBrd * C57BL/6J)
|
impaired osteoblast differentiation
|
J:188176
|
Evltm1Lfr/Evltm1Lfr
(involves: 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:94077
|
Ewsr1tm1c(EUCOMM)Wtsi/Ewsr1tm1d(EUCOMM)Wtsi Tg(Stra8-icre)1Reb/0
(involves: C57BL/6J)
|
abnormal DNA methylation during gametogenesis
|
J:314468
|
abnormal meiosis
|
J:314468
|
arrest of male meiosis
|
J:314468
|
azoospermia
|
J:314468
|
Ewsr1tm1Sblee/Ewsr1tm1Sblee
(involves: 129S6/SvEvTac * Black Swiss)
|
abnormal cell nucleus morphology
|
J:122058
|
abnormal male meiosis
|
J:122058
|
abnormal spermatid morphology
|
J:122058
|
abnormal spermatocyte morphology
|
J:122058
|
decreased spermatid number
|
J:122058
|
early cellular replicative senescence
|
J:122058
|
Ewsr1tm2(FLI1*)Sblee/Ewsr1+ Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
increased fibroblast apoptosis
|
J:156860
|
increased renal tubule apoptosis
|
J:156860
|
Exd1tm1Embrp/Exd1tm1Embrp
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JRj)
|
abnormal male germ cell physiology
|
J:229314
|
Exo1tm1Wed/Exo1tm1Wed
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal chiasmata formation
|
J:82426
|
abnormal male meiosis
|
J:82426
|
abnormal meiotic configurations
|
J:82426
|
abnormal meiotic spindle morphology
|
J:82426
|
abnormal mismatch repair
|
J:82426
|
absent chiasmata formation
|
J:82426
|
asthenozoospermia
|
J:82426
|
chromosomal instability
|
J:82426
|
decreased oocyte number
|
J:82426
|
increased male germ cell apoptosis
|
J:82426
|
oligozoospermia
|
J:82426
|
Exo1tm2Wed/Exo1tm2Wed
(involves: 129 * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:198719
|
abnormal male germ cell apoptosis
|
J:198719
|
abnormal male meiosis
|
J:198719
|
abnormal mismatch repair
|
J:198719
|
oligozoospermia
|
J:198719
|
Exo1tm2Wed/Exo1tm2Wed Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
chromosomal instability
|
J:198719
|
Exo1tm3.1Wed/Exo1tm3.1Wed
(involves: 129 * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:198719
|
Exo1tm3.1Wed/Exo1tm3.1Wed Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
abnormal chromosome stability
|
J:198719
|
Exo5em1Qsh/Exo5em1Qsh
(Not Specified)
|
oligozoospermia
|
J:307534
|
Exoc3tm2c(EUCOMM)Hmgu/Exoc3tm2c(EUCOMM)Hmgu Tg(Pf4-icre)Q3Rsko/0
(involves: C57BL/6 * C57BL/6N)
|
decreased platelet dense granule secretion
|
J:302300
|
increased platelet dense granule secretion
|
J:302300
|
Exoc7em1Utr/Exoc7em1Utr Nanos3tm2.1(cre)Ysa/Nanos3+
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal spermatocyte morphology
|
J:347251
|
azoospermia
|
J:347251
|
Exosc1em1(IMPC)J/Exosc1em1(IMPC)J
(C57BL/6NJ-Exosc1em1(IMPC)J/Mmjax)
|
increased embryonic epiblast cell apoptosis
|
J:279207,
J:343201
|
Exosc10em1Dean/Exosc10em1Dean
(involves: C57BL/6J * DBA/2J)
|
abnormal oocyte morphology
|
J:293856
|
decreased oocyte number
|
J:293856
|
Exph5tm1Tiz/Exph5tm1Tiz
(B6NJcl.Cg-Exph5tm1Tiz/Tiz)
|
oxidative stress
|
J:313415
|
Ext1tm1Yama/Ext1+ Slit2tm1Matl/Slit2tm1Matl Tg(Nes-cre)1Kln/0
(involves: 129S2/SvPas * 129S5/SvEvBrd * C57BL/6 * SJL)
|
abnormal axon guidance
|
J:86465
|
Ext1tm1Yama/Ext1tm1Yama
(B6.129S5-Ext1tm1Yama)
|
decreased cranial neural crest cell proliferation
|
J:152572
|
Ext1tm1Yama/Ext1tm1Yama H2az2Tg(Wnt1-cre)11Rth/H2az2+
(B6.Cg-H2az2Tg(Wnt1-cre)11Rth Ext1tm1Yama)
|
decreased cranial neural crest cell proliferation
|
J:152572
|
Ext1tm1Yama/Ext1tm1Yama Tg(Nes-cre)1Kln/0
(involves: 129S5/SvEvBrd * C57BL/6 * SJL)
|
abnormal axon guidance
|
J:86465
|
Extl1em1Caox/Extl1em1Caox Tg(Itgax-cre)1-1Reiz/0
(involves: C57BL/6 * CBA)
|
abnormal dendritic cell chemotaxis
|
J:333437
|
abnormal dendritic cell migration
|
J:333437
|
Extl2tm1Hkit/Extl2tm1Hkit
(B6.129P2-Extl2tm1Hkit)
|
abnormal cell morphology
|
J:197845
|
Extl3tm1.1Okam/Extl3tm1Okam Tg(Ins2-cre)#Okam/0
(involves: 129P2/OlaHsd * ICR)
|
decreased cell proliferation
|
J:148348
|
Eya1tm1Rilm/Eya1tm1Rilm
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
increased metanephric mesenchyme apoptosis
|
J:57313
|
increased otic epithelial cell apoptosis
|
J:57313
|
Eya1tm1Rilm/Eya1tm1Rilm
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased otic epithelial cell proliferation
|
J:119574
|
increased otic epithelial cell apoptosis
|
J:119574
|
Eya1tm1Rilm/Eya1tm1Rilm Six1tm1Mair/Six1tm1Mair
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:172023
|
increased apoptosis
|
J:172023
|
Eya4tm1Jse/Eya4tm1Jse
(involves: 129S6/SvEvTac * CBA/J)
|
increased middle ear goblet cell number
|
J:131873
|
Ezh1tm1Jnw/Ezh1tm1Jnw Ezh2tm1Tara/Ezh2tm1Tara Tg(KRT14-cre)1Efu/0
(involves: 129P2/OlaHsd)
|
increased hair follicle apoptosis
|
J:169295
|
Ezh1tm1Sgon/Ezh1tm1Sgon Tg(VAV1-cre)1Graf/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
early cellular replicative senescence
|
J:193722
|
Ezh2em1Jiaf/Ezh2+
(C57BL/6J-Ezh2em1Jiaf)
|
abnormal osteoblast physiology
|
J:345603
|
Ezh2tm1Jnw/Ezh2tm1Jnw
(involves: 129P2/OlaHsd)
|
absent inner cell mass proliferation
|
J:69977
|
Ezh2tm1Tara/Ezh2tm1Tara Ighg1tm1(cre)Cgn/Ighg1+
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:199122
|
Ezh2tm1Yugo/Ezh2tm1Yugo Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: 129S/Sv * C57BL/6)
|
abnormal neuron differentiation
|
J:154927
|
Ezh2tm1Yugo/Ezh2tm1Yugo Tg(Nes-cre/ERT2)5-1Imayo/0
(involves: C57BL/6)
|
abnormal neuron differentiation
|
J:154927
|
F2rtm1Ajc/F2rtm1Ajc
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell physiology
|
J:33380
|
F2rtm1Ajc/F2rtm1Ajc
(B6.129S4-F2rtm1Ajc)
|
abnormal cell physiology
|
J:76348
|
abnormal neuron apoptosis
|
J:89774
|
F2rl1tm1Cgh/F2rl1tm1Cgh
(involves: 129S4/SvJae * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:76626
|
F3tm1.1Dwr/F3tm1.1Dwr
(involves: 129S1/Sv * 129X1/SvJ * MF1 * Swiss)
|
abnormal cellular extravasation
|
J:91165
|
abnormal leukocyte adhesion
|
J:91165
|
impaired leukocyte tethering or rolling
|
J:91165
|
increased vascular smooth muscle cell proliferation
|
J:111390
|
F11tm1Gjb/F11tm1Gjb Proctm1Fjc/Proctm1Fjc
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
gangrene
|
J:67398
|
Faap20tm1(KOMP)Mbp/Faap20tm1(KOMP)Mbp
(involves: C57BL/6 * C57BL/6N)
|
abnormal cell cycle
|
J:224688
|
abnormal cell physiology
|
J:224688
|
decreased male germ cell number
|
J:224688
|
Faap100em1Jzc/Faap100em1Jzc
(involves: C57BL/6J * ICR)
|
azoospermia
|
J:339060
|
decreased primordial germ cell number
|
J:339060
|
decreased primordial germ cell proliferation
|
J:339060
|
increased primordial germ cell apoptosis
|
J:339060
|
Fabp3tm1Bin/Fabp3tm1Bin
(involves: 129P2/OlaHsd * BALB/c)
|
increased cardiac muscle cell glucose uptake
|
J:54614
|
Fabp4tm1Brsp/Fabp4tm1Brsp Fabp5tm1Hota/Fabp5tm1Hota Lepob/Lepob
(B6.Cg-Fabp4tm1Brsp Fabp5tm1Hota Lepob)
|
increased adipocyte glucose uptake
|
J:111878
|
increased muscle cell glucose uptake
|
J:111878
|
Fabp5tm1Hota/Fabp5tm1Hota
(B6.Cg-Fabp5tm1Hota)
|
increased adipocyte glucose uptake
|
J:81609
|
Fabp9tm1Vise/Fabp9tm1Vise
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal sperm head morphology
|
J:166942
|
Faddtm1Mak/Faddtm1Mak
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1))
|
decreased fibroblast apoptosis
|
J:46527
|
Faddtm1Mpa/Faddtm1Mpa Ikbkgtm1.1Mpa/Ikbkgtm1.1Mpa Tg(Alb1-cre)7Gsc/0
(involves: C57BL/6 * FVB/N)
|
decreased apoptosis
|
J:118336
|
Faddtm1Mpa/Faddtm1Mpa Mogtm1(cre)Gkl/Mog+
(involves: C57BL/6 * SJL)
|
abnormal oligodendrocyte apoptosis
|
J:167475
|
Faddtm1Mpa/Faddtm1Mpa Tg(Vil1-cre)997Gum/0
(B6.Cg-Faddtm1Mpa Tg(Vil1-cre)997Gum)
|
abnormal enterocyte proliferation
|
J:175865
|
increased enterocyte apoptosis
|
J:175865
|
Faddtm1Wnt/Faddtm1Wnt
(involves: 129S4/SvJae)
|
decreased sensitivity to induced cell death
|
J:63946
|
Faddtm1Wnt/Faddtm1Wnt Tg(Fadd/EGFP)#Jizh/? Tg(Cd4-cre)1Cwi/?
(involves: 129S4/SvJae * C57BL/6 * DBA/2)
|
decreased sensitivity to induced cell death
|
J:113207
|
Faddtm1Wnt/Faddtm1Wnt Tg(Fadd/EGFP)#Jizh/? Tg(Lck-cre)1Cwi/?
(involves: 129S4/SvJae)
|
decreased sensitivity to induced cell death
|
J:113207
|
Faddtm2.1Wnt/Faddtm2.1Wnt Tg(Cd4-cre)1Cwi/?
(B6.Cg-Tg(Cd4-cre)1Cwi Faddtm2.1Wnt)
|
abnormal T cell proliferation
|
J:162312
|
abnormal thymocyte apoptosis
|
J:162312
|
Fads1Gt(IST11525H2)Tigm/Fads1+
(C57BL/6-Fads1Gt(IST11525H2)Tigm)
|
abnormal enterocyte proliferation
|
J:186265
|
Fads1Gt(IST11525H2)Tigm/Fads1Gt(IST11525H2)Tigm
(C57BL/6-Fads1Gt(IST11525H2)Tigm)
|
abnormal enterocyte proliferation
|
J:186265
|
Fads2tm1Mtna/Fads2tm1Mtna
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal acroplaxome morphology
|
J:176697
|
abnormal acrosome assembly
|
J:176697
|
abnormal Golgi apparatus morphology
|
J:176697
|
abnormal proacrosomal vesicle fusion
|
J:176697
|
abnormal spermatid morphology
|
J:153293
|
absent acrosome
|
J:176697
|
azoospermia
|
J:153293
|
globozoospermia
|
J:176697
|
Fads2tm1Wst/Fads2tm1Wst
(involves: 129P2/OlaHsd)
|
abnormal oocyte morphology
|
J:140341
|
abnormal zona pellucida morphology
|
J:140341
|
absent zona pellucida
|
J:140341
|
azoospermia
|
J:140341
|
Faf1Gt(XK588)Byg/Faf1Gt(XK588)Byg
(B6.129P2-Faf1Gt(XK588)Byg)
|
decreased sensitivity to induced cell death
|
J:194987
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:194987
|
Fahtm1Mgo/Fahtm1Mgo
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased hepatocyte proliferation
|
J:138701
|
Fahtm1Mgo/Fahtm1Mgo
(involves: 129S7/SvEvBrd)
|
decreased hepatocyte apoptosis
|
J:105440
|
Fahtm1Mgo/Fahtm1Mgo
(involves: 129S7/SvEvBrd * C57BL)
|
abnormal hepatocyte mitochondrial morphology
|
J:27735
|
Faimtm1Kplm/Faimtm1Kplm
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell apoptosis
|
J:164184
|
increased hepatocyte apoptosis
|
J:164184
|
increased thymocyte apoptosis
|
J:164184
|
Fam3dem1Wko/Fam3dem1Wko
(C57BL/6-Fam3dem1Wko)
|
abnormal colon goblet cell morphology
|
J:300819
|
abnormal intestinal goblet cell physiology
|
J:300819
|
Fam20ctm1.1Cqi/Fam20ctm1.1Cqi Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
decreased chondrocyte apoptosis
|
J:185208
|
decreased chondrocyte proliferation
|
J:185208
|
impaired osteoblast differentiation
|
J:185208
|
Fam50aem1Zfhu/Y Stra8em1(GFP/cre)Smoc/Stra8+
(involves: C57BL/6J)
|
arrest of male meiosis
|
J:357849
|
azoospermia
|
J:357849
|
Fam50bem1Zfhu/Fam50bem1Zfhu
(C57BL/6J-Fam50bem1Zfhu)
|
abnormal outer dense fiber morphology
|
J:357849
|
abnormal sperm axoneme morphology
|
J:357849
|
abnormal sperm flagellum morphology
|
J:357849
|
absent sperm mitochondrial sheath
|
J:357849
|
asthenozoospermia
|
J:357849
|
Fam72atm1.1(KOMP)Vlcg/Fam72atm1.1(KOMP)Vlcg
(C57BL/6NTac-Fam72atm1.1(KOMP)Vlcg)
|
increased B cell apoptosis
|
J:326431
|
Fam120bem1Qqlg/Fam120bem1Qqlg
(C57BL/6-Fam120bem1Qqlg)
|
abnormal DNA repair
|
J:318650
|
decreased fetal cardiomyocyte proliferation
|
J:318650
|
Fam161aGt(462E7)Cmhd/Fam161aGt(462E7)Cmhd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal photoreceptor connecting cilium morphology
|
J:214319
|
increased retina apoptosis
|
J:214319
|
Fam170aem1Osb/Fam170aem1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal acrosome morphology
|
J:293721
|
abnormal sperm flagellum morphology
|
J:293721
|
abnormal sperm head morphology
|
J:293721
|
abnormal sperm midpiece morphology
|
J:293721
|
abnormal spermatid morphology
|
J:293721
|
absent sperm head
|
J:293721
|
decreased hyperactivated sperm motility
|
J:293721
|
decreased sperm progressive motility
|
J:293721
|
oligozoospermia
|
J:293721
|
Fam209em1Osb/Fam209em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal acrosome morphology
|
J:319865
|
asthenozoospermia
|
J:319865
|
globozoospermia
|
J:319865
|
Fam209em2Osb/Fam209em2Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal acrosome morphology
|
J:319865
|
asthenozoospermia
|
J:319865
|
globozoospermia
|
J:319865
|
Fan1em1Mem/Fan1em1Mem
(C57BL/6J-Fan1em1Mem)
|
abnormal cell nucleus morphology
|
J:298297
|
increased cellular sensitivity to alkylating agents
|
J:298297
|
Fan1em1Mem/Fan1em1Mem Htttm5Mem/Htt+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:298297
|
increased cellular sensitivity to alkylating agents
|
J:298297
|
Fan1em1Mem/Fan1em1Mem Htttm5Mem/Htt+ Mlh1tm1Rak/Mlh1tm1Rak
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
cellular phenotype
|
J:298297
|
Fan1em2Mem/Fan1+ Htttm3Mem/Htt+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:298297
|
Fan1em2Mem/Fan1em2Mem
(C57BL/6J-Fan1em2Mem)
|
abnormal cell nucleus morphology
|
J:298297
|
increased cellular sensitivity to alkylating agents
|
J:298297
|
Fan1em2Mem/Fan1em2Mem Htttm3Mem/Htt+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:298297
|
Fan1em2Mem/Fan1em2Mem Htttm5Mem/Htt+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:298297
|
Fan1tm1.1Jrou/Fan1tm1.1Jrou
(involves: 129P2/OlaHsd)
|
abnormal DNA repair
|
J:232403
|
polyploidy
|
J:232403
|
Fan1tm1a(KOMP)Wtsi/Fan1tm1a(KOMP)Wtsi
(129S1.B6-Fan1tm1a(KOMP)Wtsi)
|
increased kidney cell proliferation
|
J:242198
|
increased sensitivity to induced cell death
|
J:242198
|
Fan1tm1d(KOMP)Wtsi/Fan1tm1d(KOMP)Wtsi
(involves: C57BL/6N * FVB/N)
|
abnormal cell nucleus morphology
|
J:232402
|
increased hepatocyte karyomegaly
|
J:232402
|
polyploidy
|
J:232402
|
Fancatm1.1Wong/Fancatm1.1Wong
(involves: C57BL/6)
|
abnormal cell physiology
|
J:85108
|
decreased germ cell number
|
J:85108
|
Fancatm1a(EUCOMM)Wtsi/Fancatm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
increased sensitivity to induced cell death
|
J:188123
|
Fancatm1Faw/Fanca+
(involves: 129P2/OlaHsd * FVB)
|
induced chromosome breakage
|
J:63742
|
Fancatm1Faw/Fancatm1Faw
(involves: 129P2/OlaHsd * FVB)
|
induced chromosome breakage
|
J:63742
|
spontaneous chromosome breakage
|
J:63742
|
Fancatm1Faw/Fancatm1Faw
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal chromosome morphology
|
J:144998
|
Fancatm1Wong/Fancatm1Wong
(involves: 129S6/SvEvTac)
|
abnormal male meiosis
|
J:85108
|
decreased germ cell number
|
J:85108
|
increased male germ cell apoptosis
|
J:85108
|
Fancatm1Wong/Fancatm1Wong
(involves: C57BL/6)
|
decreased germ cell number
|
J:85108
|
Fancatm1Zqw/Fancatm1Zqw
(involves: 129P2/OlaHsd)
|
chromosome breakage
|
J:102526
|
Fancbem1Shnk/Fancbem1Shnk
(C57BL/6J-Fancbem1Shnk)
|
abnormal double-strand DNA break repair
|
J:224588
|
abnormal spermatid morphology
|
J:224588
|
abnormal spermatogonia morphology
|
J:224588
|
decreased male germ cell number
|
J:224588
|
decreased primordial germ cell number
|
J:224588
|
increased male germ cell apoptosis
|
J:224588
|
oligozoospermia
|
J:224588
|
Fancctm1Mab/Fancctm1Mab
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
increased cellular sensitivity to methylmethanesulfonate
|
J:47897
|
Fancctm1Mab/Fancctm1Mab
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased telomere length
|
J:157096
|
Fancctm1Mab/Fancctm1Mab Terttm1Leah/Terttm1Leah
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:157096
|
Fancctm1Mgo/Fancctm1Mgo
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:61512
|
decreased germ cell number
|
J:61512
|
decreased oocyte number
|
J:61512
|
induced chromosome breakage
|
J:61512
|
oligozoospermia
|
J:61512
|
spontaneous chromosome breakage
|
J:61512
|
Fancd2em1Tzh/Fancd2em1Tzh
(C57BL/6-Fancd2em1Tzh)
|
azoospermia
|
J:284566
|
increased cellular sensitivity to ionizing radiation
|
J:284566
|
Fancd2Gt(OST57859)Lex/Fancd2Gt(OST57859)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal male meiosis
|
J:146616
|
abnormal spermatocyte morphology
|
J:146616
|
oligozoospermia
|
J:146616
|
Fancd2Gt(OST57859)Lex/Fancd2Gt(OST57859)Lex
(involves: 129S5/SvEvBrd)
|
increased cellular sensitivity to DNA damaging agents
|
J:285384
|
Fancd2Gt(OST57859)Lex/Fancd2Gt(OST57859)Lex Usp1tm1.1Ada/Usp1tm1.1Ada
(involves: 129S5/SvEvBrd * C57BL/6)
|
increased cellular sensitivity to ionizing radiation
|
J:146616
|
induced chromosome breakage
|
J:146616
|
Fancd2tm1Hou/Fancd2tm1Hou
(129S4/SvJae-Fancd2tm1Hou)
|
abnormal male meiosis
|
J:84892
|
abnormal spermatocyte morphology
|
J:84892
|
oligozoospermia
|
J:84892
|
Fancd2tm1Hou/Fancd2tm1Hou
(involves: 129S4/SvJae)
|
increased sensitivity to induced cell death
|
J:188123,
J:193232
|
FanceTg(Tyr)2364E-2a2Ove/FanceTg(Tyr)2364E-2a2Ove
(FVB/N-FanceTg(Tyr)2364E-2a2Ove/Mmjax)
|
decreased male germ cell number
|
J:251511
|
Fancftm1Nki/Fancftm1Nki
(involves: 129P2/OlaHsd * FVB)
|
abnormal DNA repair
|
J:180025
|
azoospermia
|
J:180025
|
polyploidy
|
J:180025
|
Fancgtm1Ada/Fancgtm1Ada
(involves: 129S4/SvJae * C57BL/6)
|
chromosome breakage
|
J:72945
|
spontaneous chromosome breakage
|
J:72945
|
Fancgtm1Faw/Fancgtm1Faw
(involves: 129P2/OlaHsd * FVB/N)
|
chromosome breakage
|
J:74737
|
induced chromosome breakage
|
J:74737
|
spontaneous chromosome breakage
|
J:74737
|
Fanciem2Szh/Fanciem2Szh
(Not Specified)
|
abnormal DNA methylation during gametogenesis
|
J:312543
|
decreased male germ cell number
|
J:312543
|
increased male germ cell apoptosis
|
J:312543
|
oligozoospermia
|
J:312543
|
Fancitm1.1Itl/Fancitm1.1Itl
(involves: C57BL/6J * CBA)
|
abnormal fibroblast physiology
|
J:285384
|
absent gametes
|
J:285384
|
azoospermia
|
J:285384
|
early cellular replicative senescence
|
J:285384
|
increased cellular sensitivity to DNA damaging agents
|
J:285384
|
induced chromosome breakage
|
J:285384
|
spontaneous chromosome breakage
|
J:285384
|
Fanclgcd/Fanclgcd
(involves: C57BL/6J * CBA/J)
|
decreased primordial germ cell number
|
J:21254,
J:80424
|
decreased primordial germ cell proliferation
|
J:80424
|
oligozoospermia
|
J:21254
|
Fanclgcd/Fancltm1Ceb
(involves: 129/Sv * C57BL/6 * FVB/N)
|
absent germ cells
|
J:80424
|
Fancltm1Ceb/Fancltm1Ceb
(either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * FVB/N))
|
decreased male germ cell number
|
J:80424
|
Fancmem1Qsh/Fancmem1Qsh
(C57BL/6-Fancmem1Qsh)
|
abnormal spermatid morphology
|
J:301639
|
increased cellular sensitivity to DNA damaging agents
|
J:301639
|
increased male germ cell apoptosis
|
J:301639
|
Fancmtm1.1Htr/Fancmtm1.1Htr
(involves: C57BL/6 * FVB)
|
absent spermatogonia
|
J:151714
|
azoospermia
|
J:151714
|
elevated level of mitotic sister chromatid exchange
|
J:151714
|
Far1em1(IMPC)Wtsi/Far1em1(IMPC)Wtsi
(C57BL/6N-Far1em1(IMPC)Wtsi)
|
abnormal spermatocyte morphology
|
J:339470
|
azoospermia
|
J:339470
|
decreased male germ cell number
|
J:339470
|
increased male germ cell apoptosis
|
J:339470
|
multinucleated giant male germ cells
|
J:339470
|
Fars2em3Chenk/Fars2em3Chenk Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal cell morphology
|
J:339244
|
abnormal mitochondrial crista morphology
|
J:339244
|
abnormal mitochondrial physiology
|
J:339244
|
abnormal oxidative phosphorylation
|
J:339244
|
decreased cellular ATP level
|
J:339244
|
increased apoptosis
|
J:339244
|
Faslpr/Faslpr
(MRL/Mp-Faslpr)
|
abnormal T cell proliferation
|
J:8267
|
increased kidney cell proliferation
|
J:27634
|
increased mesangial cell number
|
J:28885
|
Faslpr/Faslpr
(MRL/MpJ-Faslpr/J)
|
increased mesangial cell number
|
J:127199
|
Faslpr/Faslpr
(B6.MRL-Faslpr/J)
|
decreased B cell apoptosis
|
J:135830
|
decreased hepatocyte apoptosis
|
J:135830
|
increased renal glomerulus apoptosis
|
J:132217
|
Faslpr/Faslpr
(C3.MRL-Faslpr/J)
|
increased apoptosis
|
J:106288
|
increased mesangial cell number
|
J:7454
|
Faslpr/Faslpr
(B6.MRL-Faslpr)
|
increased mesangial cell number
|
J:7454
|
Faslpr/Faslpr
(AK.MRL-Faslpr)
|
increased mesangial cell number
|
J:7454
|
Faslpr/Faslpr
(C3.MRL-Faslpr)
|
abnormal T cell proliferation
|
J:8267
|
decreased apoptosis
|
J:114219
|
decreased neuron apoptosis
|
J:124252
|
Faslpr/Faslpr
(MRL/MpJ-Faslpr)
|
abnormal leukocyte adhesion
|
J:126009
|
impaired leukocyte tethering or rolling
|
J:126009
|
Faslpr/Faslpr
(involves: MRL/Mp)
|
decreased macrophage apoptosis
|
J:154647
|
Faslpr/Faslpr Fcer1gtm1Tks/Fcer1gtm1Tks
(MRL.Cg-Fcer1gtm1Tks Faslpr)
|
increased kidney cell proliferation
|
J:106188
|
increased mesangial cell number
|
J:106188
|
Faslpr/Faslpr Ifngtm1Ts/Ifng+
(MRL.Cg-Ifngtm1Ts Faslpr)
|
abnormal macrophage chemotaxis
|
J:123834
|
increased mesangial cell number
|
J:123834
|
Faslpr/Faslpr Ifngtm1Ts/Ifngtm1Ts
(MRL.Cg-Ifngtm1Ts Faslpr)
|
abnormal macrophage chemotaxis
|
J:123834
|
Faslpr/Faslpr Irf1tm1Mak/Irf1tm1Mak
(MRL.Cg-Irf1tm1Mak Faslpr)
|
abnormal cell physiology
|
J:114771
|
Faslpr/Faslpr Raf1tm1Bacc/Raf1tm1Bacc
(involves: 129/SvHsd * 129P2/OlaHsd * C57BL/6 * MRL)
|
increased apoptosis
|
J:135681
|
Faslpr/Faslpr Selptm1Bay/Selptm1Bay
(MRL.Cg-Selptm1Bay Faslpr)
|
abnormal leukocyte adhesion
|
J:126009
|
impaired leukocyte tethering or rolling
|
J:126009
|
increased mesangial cell number
|
J:127199
|
Faslpr/Faslpr Tnfrsf9tm1Byk/Tnfrsf9tm1Byk
(MRL.Cg-Tnfrsf9tm1Byk Faslpr)
|
increased lacrimal gland apoptosis
|
J:126929
|
Fastm1Ach/Fastm1Ach Tg(Itgax-cre,-EGFP)4097Ach/?
(Not Specified)
|
decreased apoptosis
|
J:123556
|
Fastm1Cgn/Fastm1Cgn Tg(Cd4-cre)1Cwi/0
(B6.Cg-Tg(Cd4-cre)1Cwi Fastm1Cgn)
|
increased T cell apoptosis
|
J:114948
|
Fastm1Dlo/Fastm1Dlo
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal apoptosis
|
J:90750
|
Faslgld/Faslgld
(B6Smn.C3-Faslgld/J)
|
abnormal male germ cell apoptosis
|
J:146994
|
decreased hepatocyte apoptosis
|
J:135830
|
Faslgld/Faslgld
(C3H/HeJ-Faslgld)
|
abnormal T cell proliferation
|
J:8267
|
decreased neuron apoptosis
|
J:124252
|
Faslgld/Faslgld
(B6.C3-Faslgld)
|
impaired macrophage phagocytosis
|
J:91058
|
increased apoptosis
|
J:91058
|
Fasltm1.1Cgm/Fasltm1.1Cgm
(involves: 129S2/SvPas * C57BL/6 * C57BL/6N)
|
increased B cell proliferation
|
J:168406
|
increased T cell proliferation
|
J:168406
|
Fasltm2.1Bksa/Fasltm2.1Bksa
(involves: 129 * C57BL/6)
|
increased retina apoptosis
|
J:171440
|
Fat4tm1.1Hmc/Fat4tm1.1Hmc
(involves: 129P2/OlaHsd)
|
decreased kidney cell proliferation
|
J:169135
|
increased kidney apoptosis
|
J:169135
|
Fautm1.1Smoc/Fau+
(involves: 129 * C57BL/6J * FVB/N)
|
maternal effect
|
J:293342
|
Fblim1tm1.1Chen/Fblim1tm1.1Chen
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
abnormal osteoblast differentiation
|
J:186501
|
abnormal osteoclast differentiation
|
J:186501
|
decreased cell proliferation
|
J:186501
|
increased apoptosis
|
J:186501
|
Fbln1Gt(XST011)Byg/Fbln1Gt(XST011)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased hindbrain apoptosis
|
J:137690
|
Fbln5tm1Eno/Fbln5tm1Eno
(involves: 129S6/SvEvTac * C57BL/6)
|
oxidative stress
|
J:159246
|
Fbln7tm1.1Hiya/Fbln7tm1.1Hiya
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell physiology
|
J:271278
|
Fbn1Tsk Bloc1s6+/Fbn1+ Bloc1s6pa
(B6.Cg-Fbn1Tsk +/+ Bloc1s6pa/J)
|
cellular phenotype
|
J:55591
|
Fbn2tm1Rmz/Fbn2tm1Rmz
(either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6J))
|
abnormal interdigital cell death
|
J:70592
|
Fbxl4tm1.2Lrsn/Fbxl4tm1.2Lrsn
(involves: C57BL/6N)
|
abnormal oxidative phosphorylation
|
J:303084
|
decreased mitochondrial DNA content
|
J:303084
|
decreased mitochondrial number
|
J:303084
|
Fbxl5tm1Kei/Fbxl5tm1Kei
(B6.129-Fbxl5tm1Kei)
|
increased embryonic tissue cell apoptosis
|
J:176655
|
oxidative stress
|
J:176655
|
Fbxl5tm2.1Kei/Fbxl5tm2.1Kei
(involves: C57BL/6)
|
abnormal mitochondrial physiology
|
J:176655
|
oxidative stress
|
J:176655
|
Fbxl5tm2.1Kei/Fbxl5tm2.1Kei Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA)
|
abnormal hepatocyte mitochondrial morphology
|
J:176655
|
Fbxl21Psttm/Fbxl21Psttm Tg(Per2-luc)1Jt/0
(involves: C57BL/6J)
|
abnormal fibroblast physiology
|
J:194037
|
Fbxo4tm1.1Jadi/Fbxo4tm1.1Jadi
(Not Specified)
|
increased fibroblast proliferation
|
J:178645
|
Fbxo4tm1Kei/Fbxo4tm1Kei
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:183656
|
Fbxo4tm1Kei/Fbxo4tm1Kei Fbxw8tm1Kei/Fbxw8tm1Kei
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:183656
|
Fbxo5tm1Dlim/Fbxo5tm1Dlim
(involves: 129S4/SvJaeSor)
|
abnormal mitosis
|
J:110317
|
abnormal mitotic spindle morphology
|
J:110317
|
Fbxo7tm1a(EUCOMM)Wtsi/Fbxo7tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
immotile sperm
|
J:272313
|
oligozoospermia
|
J:272313
|
teratozoospermia
|
J:272313
|
Fbxo22em1Mkt/Fbxo22em1Mkt
(involves: C57BL/6N)
|
abnormal cell physiology
|
J:236274
|
decreased fibroblast proliferation
|
J:236274
|
Fbxo24em1Syu/Fbxo24em1Syu
(involves: C57BL/6J)
|
abnormal acrosome morphology
|
J:347878
|
abnormal chromatoid body morphology
|
J:347878
|
abnormal male germ cell physiology
|
J:347878
|
abnormal mitochondrial crista morphology
|
J:347878
|
abnormal mitochondrial morphology
|
J:347878
|
abnormal sperm axoneme morphology
|
J:347878
|
abnormal sperm fibrous sheath morphology
|
J:347878
|
abnormal sperm flagellum morphology
|
J:347878
|
abnormal sperm head morphology
|
J:347878
|
abnormal sperm midpiece morphology
|
J:347878
|
abnormal sperm mitochondrial sheath morphology
|
J:347878
|
abnormal sperm nucleus morphology
|
J:347878
|
abnormal spermatid morphology
|
J:347878
|
asthenozoospermia
|
J:347878
|
decreased elongated spermatid number
|
J:347878
|
decreased male germ cell number
|
J:347878
|
disorganized sperm mitochondrial sheath
|
J:347878
|
increased male germ cell apoptosis
|
J:347878
|
oligozoospermia
|
J:347878
|
Fbxo38em1Crmk/Fbxo38em1Crmk
(C57BL/6N-Fbxo38em1Crmk)
|
abnormal male meiosis
|
J:326445
|
oligozoospermia
|
J:326445
|
Fbxo41tm1(KOMP)Vlcg/Fbxo41tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal neuronal migration
|
J:222558
|
Fbxo43tm1.1Kald/Fbxo43tm1.1Kald Tg(Stra8-icre)1Reb/0
(involves: 129 * C57BL/6 * FVB/NJ * SJL)
|
arrest of male meiosis
|
J:251984
|
increased male germ cell apoptosis
|
J:251984
|
Fbxo43tm1.1Kald/Fbxo43tm1.2Kald Gt(ROSA)26Sortm1(cre/ERT)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL)
|
increased male germ cell apoptosis
|
J:251984
|
Fbxo43tm1.2Kald/Fbxo43tm1.2Kald
(involves: 129 * C57BL/6 * FVB/N * SJL)
|
abnormal female meiosis
|
J:251984
|
abnormal oocyte morphology
|
J:251984
|
arrest of male meiosis
|
J:251984
|
azoospermia
|
J:251984
|
increased male germ cell apoptosis
|
J:251984
|
parthenogenesis
|
J:251984
|
Fbxo45tm1Kei/Fbxo45tm1Kei
(B6.129P2-Fbxo45tm1Kei)
|
abnormal axon fasciculation
|
J:149890
|
abnormal neuronal migration
|
J:149890
|
Fbxo47em1Keish/Fbxo47em1Keish
(C57BL/6N-Fbxo47em1Keish)
|
abnormal synaptonemal complex
|
J:322322
|
abnormal X-Y chromosome synaptonemal complex assembly during male meiosis
|
J:322322
|
azoospermia
|
J:322322
|
increased male germ cell apoptosis
|
J:322322
|
Fbxw5em1Syli/Fbxw5em1Syli
(C57BL/6-Fbxw5em1Syli)
|
cardiac interstitial fibrosis
|
J:298305
|
Fbxw7tm1.1Axbe/Fbxw7tm1.1Axbe Juntm4Wag/Jun+ Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal neuron apoptosis
|
J:166928
|
Fbxw7tm1.1Axbe/Fbxw7tm1.1Axbe Notch1tm1Agt/Notch1+ Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:166928
|
Fbxw7tm1.1Axbe/Fbxw7tm1.1Axbe Tg(En2-cre)22Alj/0
(Not Specified)
|
abnormal neuron differentiation
|
J:176598
|
Fbxw7tm1.1Axbe/Fbxw7tm1.1Axbe Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:166928
|
Fbxw7tm1Iaai/Fbxw7tm1Iaai Tg(Amh-cre)8815Reb/0
(involves: 129 * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal male germ cell physiology
|
J:289161
|
decreased male germ cell number
|
J:289161
|
increased male germ cell apoptosis
|
J:289161
|
oligozoospermia
|
J:289161
|
Fbxw7tm1Kei/Fbxw7tm1Kei Tg(Lck-cre)1Cwi/?
(involves: 129P2/OlaHsd * C57BL/6)
|
increased T cell apoptosis
|
J:128523
|
Fbxw8tm1Kei/Fbxw8tm1Kei
(Not Specified)
|
cellular phenotype
|
J:183656
|
Fbxw11tm2Nakay/Fbxw11tm1Nakay
(B6.Cg-Fbxw11tm2Nakay Fbxw11tm1Nakay)
|
decreased fibroblast proliferation
|
J:228222
|
Fcer1gtm1Rav/Fcer1gtm1Rav
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired macrophage phagocytosis
|
J:39248
|
Fcer1gtm1Rav/Fcer1gtm1Rav Hexbtm1Rlp/Hexbtm1Rlp
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
decreased apoptosis
|
J:87617
|
Fcer1gtm1Rav/Fcer1gtm1Rav Tg(Ins2-TFRC/OVA)296Wehi/0
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:122114
|
Fcer1gtm1Rav/Fcer1gtm1Rav Tyrobptm1Lll/Tyrobptm1Lll
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:89583
|
Fcer1gtm1Tks/Fcer1gtm1Tks
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:112160
|
impaired macrophage phagocytosis
|
J:50023
|
Fcer2atm1Max/Fcer2atm1Max
(involves: C57BL/6)
|
abnormal macrophage chemotaxis
|
J:57738
|
Fcer2atm1Putt/Fcer2atm1Putt
(involves: 129S/SvEv * C57BL/6)
|
abnormal B cell proliferation
|
J:69547
|
Fcgr1tm1Hoga/Fcgr1tm1Hoga
(involves: 129S1/Sv * 129X1/SvJ)
|
impaired macrophage phagocytosis
|
J:86281
|
Fcgr1tm1Jgjw/Fcgr1tm1Jgjw
(involves: 129 * C57BL/6)
|
abnormal dendritic cell differentiation
|
J:112436
|
Fcgr1tm1Jsv/Fcgr1tm1Jsv Fcgr2btm1Ttk/Fcgr2btm1Ttk Fcgr3tm1Jsv/Fcgr3tm1Jsv
(involves: 129P2/OlaHsd * 129S4/SvJae * BALB/c * C57BL/6)
|
impaired macrophage phagocytosis
|
J:83995
|
Fcgr2btm1Kgcs/Fcgr2b+
(involves: C57BL/6)
|
decreased B cell apoptosis
|
J:190890
|
Fcgr3tm1Jsv/Fcgr3tm1Jsv
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased mast cell degranulation
|
J:35057
|
impaired macrophage phagocytosis
|
J:35057
|
Fcmrtm1.2Khl/Fcmrtm1.2Khl
(involves: C57BL/6)
|
increased T cell apoptosis
|
J:174871
|
Fcs1Pohnpei/Fcs1Pohnpei
(involves: C57BL/6J * Pohnpei)
|
increased cell proliferation
|
J:114559
|
Fcs2Pohnpei/Fcs2Pohnpei
(involves: C57BL/6J * Pohnpei)
|
decreased cell proliferation
|
J:114559
|
Fcs3C57BL/6J/Fcs3Pohnpei Fcs4Pohnpei/Fcs4Pohnpei
(involves: C57BL/6J * Pohnpei)
|
increased cell proliferation
|
J:114559
|
Fcs3Pohnpei/Fcs3Pohnpei Fcs4C57BL/6J/Fcs4Pohnpei
(involves: C57BL/6J * Pohnpei)
|
increased cell proliferation
|
J:114559
|
Fcs3Pohnpei/Fcs3Pohnpei Fcs4Pohnpei/Fcs4Pohnpei
(involves: C57BL/6J * Pohnpei)
|
decreased cell proliferation
|
J:114559
|
Fdpstm1Jiy/Fdpstm1Jiy Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6 * FVB/N)
|
abnormal autophagy
|
J:317808
|
cardiac interstitial fibrosis
|
J:317808
|
Fdx1tm1Xch/Fdx1+
(involves: C57BL/6)
|
abnormal cell morphology
|
J:345826
|
Fdxrm1J/Fdxrm1J Otop2m1J/Otop2m1J
(B6;129S-Fdxrm1J Otop2m1J/GrsrJ)
|
abnormal mitochondrial crista morphology
|
J:247931
|
abnormal mitochondrial morphology
|
J:247931
|
Fdxrtm1Xch/Fdxr+
(B6.Cg-Fdxrtm1Xch)
|
abnormal mitochondrial morphology
|
J:244082
|
decreased cell death
|
J:244082
|
increased fibroblast proliferation
|
J:244082
|
Fen1tm1Bhsh/Fen1tm1Bhsh
(involves: 129S1/Sv)
|
abnormal fibroblast physiology
|
J:121378
|
decreased cell proliferation
|
J:121378
|
Fen1tm1Klng/Fen1tm1Klng
(involves: C57BL/6)
|
abnormal DNA repair
|
J:84556
|
decreased DNA replication
|
J:84556
|
increased cellular sensitivity to gamma-irradiation
|
J:84556
|
Fen1tm1Rak/Fen1+ Apctm1Rak/Apc+
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * SJL/J)
|
abnormal cell physiology
|
J:77962
|
Fen1tm2.1Bhsh/Fen1+
(involves: 129S1/Sv)
|
aneuploidy
|
J:218627
|
decreased fibroblast proliferation
|
J:218627
|
spontaneous chromosome breakage
|
J:218627
|
Fen1tm2.1Bhsh/Fen1tm2.1Bhsh
(involves: 129S1/Sv)
|
abnormal cell physiology
|
J:218627
|
abnormal double-strand DNA break repair
|
J:218627
|
abnormal telomere morphology
|
J:218627
|
aneuploidy
|
J:218627
|
chromosomal instability
|
J:218627
|
decreased fibroblast proliferation
|
J:218627
|
spontaneous chromosome breakage
|
J:218627
|
Fen1tm2Klng/Fen1tm2Klng
(involves: 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:138901
|
Fen1tm3.1Bhsh/Fen1+
(Not Specified)
|
chromosomal instability
|
J:231218
|
increased cellular sensitivity to methylmethanesulfonate
|
J:231218
|
increased sensitivity to induced cell death
|
J:231218
|
Fen1tm3.1Bhsh/Fen1tm3.1Bhsh
(Not Specified)
|
abnormal cell physiology
|
J:231218
|
chromosomal instability
|
J:231218
|
increased cellular sensitivity to methylmethanesulfonate
|
J:231218
|
increased kidney apoptosis
|
J:231218
|
increased lung apoptosis
|
J:231218
|
increased sensitivity to induced cell death
|
J:231218
|
Fen1tm3Klng/Fen1tm3Klng
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:138901
|
Fendrrtm1Bgh/Fendrrtm2Bgh
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:191565
|
Ferd3ltm1Yono/Ferd3ltm1Yono
(involves: C57BL/6)
|
abnormal neuron differentiation
|
J:160534
|
abnormal neuronal precursor proliferation
|
J:160534
|
Fermt1tm1Ref/Fermt1tm1Ref
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased keratinocyte adhesion
|
J:142913
|
decreased keratinocyte proliferation
|
J:142913
|
Fermt2tm1.1Gxo/Fermt2tm1.1Gxo Tg(Prrx1-cre)1Cjt/0
(B6.Cg-Fermt2tm1.1Gxo Tg(Prrx1-cre)1Cjt)
|
decreased chondrocyte proliferation
|
J:224370
|
increased chondrocyte apoptosis
|
J:224370
|
Fermt2tm1Ref/Fermt2tm1Ref
(Not Specified)
|
abnormal cell adhesion
|
J:134768
|
Fetubtm1Wja/Fetubtm1Wja
(B6.Cg-Fetubtm1Wja)
|
abnormal zona pellucida morphology
|
J:196435
|
Fetubtm1Wja/Fetubtm1Wja
(D2.Cg-Fetubtm1Wja)
|
abnormal zona pellucida morphology
|
J:196435
|
Fevtm1Esd/Fevtm1Esd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal neuron differentiation
|
J:81450
|
Fezf1tm1Hibi/Fezf1tm1Hibi
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal neuronal migration
|
J:107405
|
Fezf1tm1Taku/Fezf1tm1Taku
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal axon extension
|
J:174482
|
Fezf2tm1Hibi/Fezf2tm1Hibi
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal axon guidance
|
J:214959
|
Fezf2tm1Skm/Fezf2tm1Skm
(involves: 129 * CD-1)
|
abnormal axon guidance
|
J:103829
|
Ffar2tm1Dgen/Ffar2tm1Dgen
(involves: C57BL/6)
|
impaired neutrophil chemotaxis
|
J:153951
|
impaired neutrophil phagocytosis
|
J:153951
|
Ffar2tm2Lex/Ffar2tm2Lex
(involves: 129S7/SvEvBrd * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:157383
|
Ffar4tm1(KOMP)Vlcg/Ffar4tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal brown fat cell differentiation
|
J:240649
|
abnormal white fat cell differentation
|
J:240649
|
Fgf2tm1Doe/Fgf2tm1Doe
(involves: 129P2/OlaHsd * Black Swiss)
|
abnormal neuron differentiation
|
J:126024
|
increased cardiomyocyte apoptosis
|
J:119652
|
Fgf2tm1Doe/Fgf2tm1Doe
(B6.129P2-Fgf2tm1Doe)
|
abnormal vascular endothelial cell migration
|
J:114567
|
Fgf2tm1Zllr/Fgf2tm1Zllr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuronal migration
|
J:49141
|
Fgf2tm1Zllr/Fgf2tm1Zllr Fgf6tm1Thbr/Fgf6tm1Thbr
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
abnormal myoblast migration
|
J:85088
|
Fgf2tm2Doe/Fgf2tm2Doe
(involves: 129P2/OlaHsd * Black Swiss)
|
increased cardiomyocyte apoptosis
|
J:119652
|
Fgf4tm1Gol/Fgf4tm1Gol
(involves: C57BL/6J)
|
decreased inner cell mass proliferation
|
J:22275
|
Fgf6tm1Thbr/Fgf6tm1Thbr
(either: (involves: 129S4/SvJae-Fgf6tm1Thbr) or (involves: 129S4/SvJae * C57BL/6))
|
abnormal cell migration
|
J:85088
|
Fgf8tm1.1Mrt/Fgf8tm1.4Mrt
(involves: 129P2/OlaHsd)
|
decreased neuron apoptosis
|
J:111586
|
Fgf8tm1.1Mrt/Fgf8tm1.4Mrt Foxg1tm1(cre)Skm/Foxg1+
(involves: 129P2/OlaHsd)
|
increased neuron apoptosis
|
J:111586
|
Fgf8tm1.1Mrt/Fgf8tm1.4Mrt Foxg1tm1M/Foxg1+
(involves: 129P2/OlaHsd)
|
abnormal neuron apoptosis
|
J:111586
|
Fgf8tm1.2Mrt/Fgf8tm1.3Mrt Foxg1tm1(cre)Skm/Foxg1+
(involves: 129P2/OlaHsd)
|
abnormal pillar cell differentiation
|
J:122378
|
Fgf8tm1.2Mrt/Fgf8tm1.3Mrt Tg(Nes-cre)1Atp/0
(involves: 129P2/OlaHsd * FVB/N)
|
increased apoptosis
|
J:58999
|
Fgf8tm1.3Mrt/Fgf8tm1.4Mrt Foxg1tm1(cre)Skm/Foxg1+
(involves: 129P2/OlaHsd)
|
increased neuron apoptosis
|
J:111586
|
Fgf8tm1.3Mrt/Fgf8tm1.4Mrt Tg(T-cre)1Lwd/0
(involves: 129P2/OlaHsd * C3H * C57BL/6 * CD-1)
|
increased kidney apoptosis
|
J:101175
|
Fgf8tm1.3Mrt/Fgf8tm2Mrt Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129 * 129S7/SvEvBrd)
|
decreased mitotic index
|
J:109474
|
Fgf8tm1Moon/Fgf8tm1Moon Mesp1tm2(cre)Ysa/Mesp1+
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal cardiac neural crest cell migration
|
J:170879
|
Fgf8tm1Mrc/Fgf8tm1Moon Hoxa3tm1(cre)Moon/Hoxa3+
(involves: 129/Sv * C57BL/6)
|
abnormal neural crest cell apoptosis
|
J:87304
|
Fgf8tm1Mrc/Fgf8tm1Moon Tfap2atm1(cre)Moon/Tfap2a+
(involves: 129/Sv * C57BL/6)
|
abnormal neural crest cell apoptosis
|
J:87304
|
Fgf8tm1Mrc/Fgf8tm2Mrc Hoxa3tm1(cre)Moon/Hoxa3+
(involves: 129/Sv * C57BL/6)
|
abnormal neural crest cell apoptosis
|
J:87304
|
Fgf8tm1Mrc/Fgf8tm2Mrc Tfap2atm1(cre)Moon/Tfap2a+
(involves: 129/Sv * C57BL/6)
|
abnormal neural crest cell apoptosis
|
J:87304
|
Fgf8tm1Mrc/Fgf8tm3Mrc
(involves: 129 * C57BL/6)
|
abnormal neural crest cell apoptosis
|
J:87304
|
Fgf8tm2Moon/Fgf8tm1Mrc Isl1tm1(cre)Sev/Isl1+
(involves: 129S/Sv)
|
increased apoptosis
|
J:109475
|
Fgf8tm2Moon/Fgf8tm1Mrc Mesp1tm2(cre)Ysa/Mesp1+
(involves: C57BL/6 * CBA)
|
decreased cell proliferation
|
J:109475
|
increased apoptosis
|
J:109475
|
Fgf9tm1Dor/Fgf9tm1Dor
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal mesenchymal cell proliferation involved in lung development
|
J:69852
|
Fgf9tm1Dor/Fgf9tm1Dor
(involves: C57BL/6J)
|
abnormal fetal cardiomyocyte proliferation
|
J:95803
|
Fgf10Mhdaaey17/Fgf10+
(involves: C3HeB/FeJ * C57BL/6)
|
abnormal retina apoptosis
|
J:154551
|
Fgf10tm1Ska/Fgf10tm1Ska
(involves: C57BL/6 * CBA)
|
increased hair follicle apoptosis
|
J:114183
|
Fgf10tm1Ska/Fgf10tm1Ska Fgf8tm1Moon/Fgf8tm1Moon Mesp1tm2(cre)Ysa/Mesp1+
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal cardiac neural crest cell migration
|
J:170879
|
Fgf10tm1Wss/Fgf10tm1Wss
(involves: 129X1/SvJ * CF-1)
|
abnormal vestibular hair cell kinocilium morphology
|
J:83738
|
Fgf13em1Xuzh/Y
(involves: C57BL/6J)
|
abnormal axon extension
|
J:307501
|
abnormal neuron differentiation
|
J:307501
|
abnormal neuronal migration
|
J:307501
|
Fgf13tm1Xuzh/Fgf13tm1Xuzh
(involves: 129)
|
abnormal neuronal migration
|
J:186253
|
Fgf15tm1Sms/Fgf15tm1Sms Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal cardiac neural crest cell migration
|
J:97317
|
Fgf16tm1Nit/Y
(C57BL/6-Fgf16tm1Nit)
|
abnormal fetal cardiomyocyte proliferation
|
J:139637
|
Fgf18tm1Dor/Fgf18tm1Dor
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal osteoblast differentiation
|
J:75879
|
Fgfr1tm1Jpa/Fgfr1tm1Jpa Fgfr2tm1Dor/Fgfr2tm1Dor Tg(Pax3-cre)1Joe/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
decreased kidney cell proliferation
|
J:107078
|
increased kidney apoptosis
|
J:107078
|
increased metanephric mesenchyme apoptosis
|
J:107078
|
Fgfr1tm1Jpa/Fgfr1tm1Jpa Fgfr2tm3.1Lni/Fgfr2tm3.1Lni Tg(Pax3-cre)1Joe/0
(involves: 129/Sv * BALB/c * C57BL/6 * FVB/N * SJL)
|
increased metanephric mesenchyme apoptosis
|
J:167305
|
Fgfr1tm1Upir/Fgfr1tm1.1Upir
(involves: C57BL/6J)
|
abnormal fetal cardiomyocyte proliferation
|
J:95803
|
Fgfr1tm1Upir/Fgfr1tm1Upir Fgfr2tm1Dor/Fgfr2tm1Dor Tg(KRT5-cre)5132Jlj/0
(involves: 129X1/SvJ * C57BL/6 * C57BL/6J * DBA/2J)
|
increased keratinocyte proliferation
|
J:158802,
J:221184
|
Fgfr1tm1Upir/Fgfr1tm1Upir Tg(GFAP-cre)25Mes/0
(involves: FVB/N)
|
abnormal neuronal migration
|
J:110263
|
Fgfr1tm1Upir/Fgfr1tm1Upir Tg(Mnx1-GFP)1Slp/? Tg(Nes-cre)1Kln/?
(Not Specified)
|
abnormal axon guidance
|
J:122940
|
Fgfr1tm2.1Cxd/Fgfr1+
(involves: 129S6/SvEvTac * FVB/N)
|
increased osteoblast proliferation
|
J:63959
|
Fgfr1tm2Jrt/Fgfr1tm2Jrt
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
abnormal neural crest cell migration
|
J:81179
|
Fgfr1tm10.1Sor/Fgfr1tm10.1Sor
(129S4/SvJaeSor-Fgfr1tm10.1Sor)
|
abnormal neural crest cell migration
|
J:226497
|
Fgfr2tm1Dor/Fgfr2+ Fgfr3tm6.1Cxd/Fgfr3tm6.1Cxd Foxg1tm1(cre)Skm/Foxg1+ Fgfr1tm1Jpa/Fgfr1tm1Jpa Frs3tm1Jheb/Frs3tm1Jheb
(involves: 129)
|
cellular phenotype
|
J:242687
|
Fgfr2tm1Dor/Fgfr2tm1.1Dor Twist2tm1(cre)Dor/Twist2+
(involves: 129X1/SvJ)
|
abnormal osteoblast physiology
|
J:90391
|
abnormal osteoclast differentiation
|
J:90391
|
decreased cell proliferation
|
J:90391
|
Fgfr2tm1Dor/Fgfr2tm1Dor Fgfr3tm6.1Cxd/Fgfr3tm6.1Cxd Foxg1tm1(cre)Skm/Foxg1+ Fgfr1tm3.1Sor/Fgfr1tm1Jpa Frs3tm1Jheb/Frs3tm1Jheb
(involves: 129)
|
cellular phenotype
|
J:242687
|
increased cell death
|
J:242687
|
Fgfr2tm1Dsn/Fgfr2tm1Dsn Tg(KRT5-cre)5132Jlj/0
(involves: 129P2/OlaHsd * C57BL/6J * DBA/2J)
|
increased keratinocyte proliferation
|
J:119723
|
Fgfr2tm1Ewj/Fgfr2+ Tg(EIIa-cre)C5379Lmgd/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N)
|
abnormal osteoblast differentiation
|
J:101174
|
Fgfr2tm1Ewj/Fgfr2+ Tg(EIIa-cre)C5379Lmgd/0
(B6.Cg-Fgfr2tm1Ewj Tg(EIIa-cre)C5379Lmgd)
|
enhanced osteoblast differentiation
|
J:158773
|
increased osteoblast proliferation
|
J:158773
|
Fgfr2tm2Ewj/Fgfr2+ Tg(EIIa-cre)C5379Lmgd/0
(B6.Cg-Fgfr2tm2Ewj Tg(EIIa-cre)C5379Lmgd)
|
enhanced osteoblast differentiation
|
J:158773
|
increased osteoblast proliferation
|
J:158773
|
Fgfr2tm3.1Cxd/Fgfr2+
(involves: 129S6/SvEvTac * FVB/N)
|
enhanced osteoblast differentiation
|
J:283626
|
Fgfr2tm3.1Lni/Fgfr2tm3.1Lni
(involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6)
|
abnormal osteoblast proliferation
|
J:77698
|
Fgfr2tm4Lni/Fgfr2tm4Lni
(Not Specified)
|
abnormal osteoblast physiology
|
J:92433
|
Fgfr3tm1.1(FGFR3*)Ytc/Fgfr3+
(involves: 129)
|
decreased chondrocyte proliferation
|
J:287271
|
Fgfr3tm1.1(FGFR3*)Ytc/Fgfr3tm1.1(FGFR3*)Ytc
(involves: 129)
|
decreased chondrocyte proliferation
|
J:287271
|
Fgfr3tm1.1Aomw/Fgfr3+
(129S6.129P2-Fgfr3tm1.1Aomw)
|
abnormal organ of Corti supporting cell differentiation
|
J:143356
|
Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw
(129S6.129P2-Fgfr3tm1.1Aomw)
|
abnormal organ of Corti supporting cell differentiation
|
J:143356
|
Fgfr3tm1.1Iwa/Fgfr3+
(involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss)
|
abnormal chondrocyte proliferation
|
J:70061
|
Fgfr3tm1Dor/Fgfr3tm1Dor
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal pillar cell differentiation
|
J:32991
|
Fgfr3tm1Dor/Fgfr3tm1Dor
(CBACa.129S6(B6)-Fgfr3tm1Dor)
|
abnormal pillar cell differentiation
|
J:117235
|
Fgfr3tm3.1Cxd/Fgfr3tm3.1Cxd
(involves: 129S6/SvEvTac)
|
decreased chondrocyte proliferation
|
J:69849
|
enhanced osteoblast differentiation
|
J:69849
|
Fgfr3tm4.1Cxd/Fgfr3+
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
abnormal osteoblast physiology
|
J:63198
|
increased chondrocyte proliferation
|
J:63198
|
increased fibroblast proliferation
|
J:63198
|
Fgfr4tm1Axul/Fgfr4tm1Axul
(B6.129P2-Fgfr4tm1Axul)
|
abnormal cell physiology
|
J:156750
|
cellular phenotype
|
J:156750
|
Fgfrl1tm1True/Fgfrl1tm1True
(B6.129S6-Fgfrl1tm1True)
|
decreased kidney cell proliferation
|
J:153202
|
increased kidney apoptosis
|
J:153202
|
Fgl2tm1Pam/Fgl2tm1Pam
(B6.129X1-Fgl2tm1Pam)
|
decreased dendritic cell apoptosis
|
J:130895
|
increased T cell proliferation
|
J:130895
|
Fgrtm1Hev/Fgrtm1Hev Hcktm1Hev/Hcktm1Hev
(involves: 129S7/SvEvBrd * C57BL/6J)
|
impaired macrophage phagocytosis
|
J:16994
|
Fh1tm1Pjp/Fh1tm1Pjp Tg(Cdh16-cre)91Igr/0
(involves: 129X1/SvJ * ICR)
|
abnormal fibroblast physiology
|
J:198486
|
abnormal tricarboxylic acid cycle
|
J:198486
|
Fhl5tm1Saco/Fhl5tm1Saco
(involves: 129S2/SvPas * C57BL/6)
|
abnormal acrosome morphology
|
J:91483
|
abnormal sperm head morphology
|
J:91483
|
abnormal sperm nucleus morphology
|
J:91483
|
asthenozoospermia
|
J:91483
|
detached acrosome
|
J:91483
|
hairpin sperm flagellum
|
J:91483
|
oligozoospermia
|
J:91483
|
teratozoospermia
|
J:91483
|
Figlatm1Dean/Figlatm1Dean
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:294629
|
abnormal female meiosis
|
J:294629
|
abnormal female meiosis I arrest
|
J:294629
|
abnormal oogenesis
|
J:294629
|
decreased oocyte number
|
J:64677
|
increased female germ cell apoptosis
|
J:294629
|
increased ovary apoptosis
|
J:294629
|
Fignfi/Fignfi
(mixed)
|
abnormal cell cycle
|
J:5736
|
Fignfi/Fignfi Vsx2or/Vsx2or
(involves: C57BL/Gr)
|
abnormal cell cycle checkpoint function
|
J:5575
|
Fignl1tm1Osb/Fignl1tm1.1Osb Spo11tm1Mjn/Spo11tm1Mjn Tg(Stra8-cre)1Osb/0
(involves: 129X1/SvJ * C57BL/6)
|
arrest of male meiosis
|
J:342157
|
Fignl1tm1Osb/Fignl1tm1.1Osb Swsap1tm1.1Osb/Swsap1tm1.1Osb Tg(Stra8-cre)1Osb/0
(involves: C57BL/6)
|
abnormal male meiosis
|
J:342157
|
Fignl1tm1Osb/Fignl1tm1.1Osb Tg(Stra8-cre)1Osb/0
(involves: C57BL/6)
|
abnormal chromosomal synapsis
|
J:342157
|
arrest of male meiosis
|
J:342157
|
oligozoospermia
|
J:342157
|
Fignl2tm1.1Geno/Fignl2tm1.1Geno
(involves: C57BL/6)
|
abnormal axon extension
|
J:309596
|
Filip1lem1Slib/Filip1lem1Slib Tg(CDX2-cre/ERT2)752Erf/0
(involves: C57BL/6J * SJL/J)
|
abnormal enterocyte proliferation
|
J:312351
|
abnormal intestinal goblet cell physiology
|
J:312351
|
increased colon goblet cell number
|
J:312351
|
Firrmem1Gpt/Firrmem1Gpt Stra8em1(GFP/cre)Smoc/Stra8+
(involves: C57BL/6JGpt)
|
abnormal chromosomal synapsis
|
J:344887
|
abnormal female meiosis
|
J:344887
|
abnormal male meiosis
|
J:344887
|
abnormal synaptonemal complex
|
J:344887
|
absent oocytes
|
J:344887
|
arrest of male meiosis
|
J:344887
|
azoospermia
|
J:344887
|
decreased male germ cell number
|
J:344887
|
decreased oocyte number
|
J:344887
|
increased male germ cell apoptosis
|
J:344887
|
Fis1tm1.1Itl/Fis1tm1.1Itl Tg(CAG-EGFP/Map1lc3b)53Nmz/0 Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6NCrlj * C57BL/6NTac * DBA/2 * FVB)
|
abnormal autophagy
|
J:290485
|
Fis1tm1.1Itl/Fis1tm1.1Itl Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6NTac * FVB)
|
abnormal mitochondrial crista morphology
|
J:290485
|
abnormal mitochondrial physiology
|
J:290485
|
increased mitochondrial size
|
J:290485
|
Fis1tm1Dcc/Fis1tm1.1Dcc Gt(ROSA)26Sortm1.1(CAG-COX8A/Dendra2)Dcc/Gt(ROSA)26Sor+ Tg(Stra8-icre)1Reb/0
(involves: 129S6/SvEvTac * C57BL/6 * FVB/NJ)
|
abnormal spermatid morphology
|
J:309044
|
azoospermia
|
J:309044
|
impaired autophagy
|
J:309044
|
increased male germ cell apoptosis
|
J:309044
|
increased mitochondrial number
|
J:309044
|
multinucleated giant male germ cells
|
J:309044
|
Fkbp1atm1Slh/Fkbp1atm1Slh Tg(Ckmm-cre)5Khn/0
(involves: 129S7/SvEvBrd * FVB)
|
oxidative stress
|
J:176731
|
Fkbp4tm1Dvds/Fkbp4tm1Dvds
(involves: 129X1/SvJ * C57BL/6)
|
asthenozoospermia
|
J:98554
|
Fkbp4tm1Dvds/Fkbp4tm1Dvds
(either: (involves: CD-1) or (involves: 129X1/SvJ * C57BL/6))
|
hairpin sperm flagellum
|
J:118360
|
oligozoospermia
|
J:118360
|
Fkbp4tm1Shou/Fkbp4tm1Shou
(involves: 129S/SvEv)
|
abnormal sperm motility
|
J:120960
|
Fkbp6tm1Pngr/Fkbp6tm1Pngr
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal spermatocyte morphology
|
J:83634
|
arrest of male meiosis
|
J:83634
|
azoospermia
|
J:83634
|
Fkbp8Gt(OST287985)Lex/Fkbp8Gt(OST287985)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
increased neural tube apoptosis
|
J:132031
|
Fkbp8tm1Kei/Fkbp8tm1Kei
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:132541
|
Fkbp8tm1Kei/Fkbp8tm1Kei
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal neuron differentiation
|
J:132961
|
Fkbp10tm2a(EUCOMM)Wtsi/Fkbp10tm2a(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal cell morphology
|
J:213596
|
abnormal endoplasmic reticulum morphology
|
J:213596
|
abnormal extracellular matrix morphology
|
J:213596
|
Fkrptm1Itl/Fkrptm1Itl
(involves: 129S6/SvEvTac * C57BL/6N)
|
abnormal neuronal migration
|
J:164448
|
Fkrptm1Scbr/?
(Not Specified)
|
abnormal radial glial cell morphology
|
J:258757
|
Fkrptm1Scbr/Fkrptm1Scbr
(involves: C57BL/6)
|
abnormal radial glial cell morphology
|
J:164634
|
Fktntm1Ttd/Fktntm1Ttd
(involves: 129S7/SvEvBrd * C57BL/6)
|
impaired basement membrane formation
|
J:97950
|
increased embryonic epiblast cell apoptosis
|
J:97950
|
Fktntm1Ttd/Fktntm2(FCMD)Ttd
(involves: 129S7/SvEvBrd)
|
abnormal neuronal migration
|
J:144746
|
Flcntm1Baba/Flcntm1.1Lss Tg(Cdh16-cre)91Igr/0
(involves: C57BL/6 * FVB/N * ICR * SJL)
|
increased kidney cell proliferation
|
J:130978
|
Flgft/Flgft
(B6.Cg-Flgft)
|
increased splenocyte proliferation
|
J:151110
|
Fli1tm1.1Dkw/Fli1tm1.1Dkw
(B6.129S6-Fli1tm1.1Dkw)
|
decreased B cell proliferation
|
J:137876
|
Fli1tm1Morl/Fli1tm1.1Morl Tg(Mx1-cre)1Cgn/0
(involves: 129/Sv * C57BL/6 * CBA * DBA)
|
abnormal megakaryocyte differentiation
|
J:167426
|
Fli1tm1Morl/Fli1tm1Morl Tg(Mx1-cre)1Cgn/0
(involves: 129/Sv * C57BL/6 * CBA)
|
abnormal megakaryocyte differentiation
|
J:167426
|
Flnatm1.2Caw/Y
(involves: 129S4/SvJae * C57BL/6)
|
abnormal vascular regression
|
J:118252
|
FlnbGt(BGB085)Byg/FlnbGt(BGB085)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:120066
|
decreased fibroblast cell migration
|
J:120066
|
Flnbtm1Vshn/Flnbtm1Vshn
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell adhesion
|
J:125095
|
abnormal extracellular matrix morphology
|
J:125095
|
Flot1tm1.1Arte/Flot1tm1.1Arte
(involves: C57BL/6J)
|
impaired neutrophil chemotaxis
|
J:166672
|
Flot2tm1Mak/Flot2tm1Mak
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell morphology
|
J:203238
|
Flrt2tm1.1Kln/Flrt2tm1.1Kln
(involves: BALB/c * C57BL/6 * CD-1)
|
abnormal neuronal migration
|
J:196042
|
Flrt3tm1Kln/Flrt3tm2Kln
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6)
|
abnormal basement membrane morphology
|
J:142039
|
Flrt3tm1Rob/Flrt3tm1Rob
(involves: 129S/SvEv)
|
impaired basement membrane formation
|
J:171515
|
Flrt3tm2Kln/Flrt3tm2Kln
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6)
|
abnormal basement membrane morphology
|
J:142039
|
Flt1tm1.1Fong/Flt1tm1.1Fong Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+
(involves: 129S6/SvEvTac * C57BL/6NCr * CD-1)
|
increased endothelial cell proliferation
|
J:202202
|
Flt1tm1Msh/Flt1tm1Msh
(involves: 129S4/SvJae * C57BL/6J)
|
impaired macrophage chemotaxis
|
J:49507
|
Flt1tm2Msh/Flt1tm2Msh Kdrtm1Jrt/Kdr+
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal vascular endothelial cell differentiation
|
J:95387
|
abnormal vascular endothelial cell migration
|
J:95387
|
Flt1tm2Msh/Flt1tm2Msh Kdrtm1Jrt/Kdrtm1Jrt
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal vascular endothelial cell migration
|
J:95387
|
Flt3tm1Dosm/Flt3+ Tg(Mx1-cre)1Cgn/0
(B6.Cg-Flt3tm1Dosm Tg(Mx1-cre)1Cgn)
|
delayed cellular replicative senescence
|
J:133528
|
Flt3ltm1Imx/Flt3ltm1Imx
(involves: C57BL/6)
|
abnormal dendritic cell chemotaxis
|
J:223508
|
Flvcr2tm1.1Tda/Flvcr2tm1.1Tda Tg(Cdh5-cre/ERT2)1Rha/0
(involves: C57BL/6J)
|
decreased endothelial cell proliferation
|
J:287134
|
Flvcr2tm1.2Tda/Flvcr2tm1.2Tda
(involves: C57BL/6J)
|
decreased endothelial cell proliferation
|
J:287134
|
fm/fm
(involves: CBA/H)
|
abnormal endoplasmic reticulum morphology
|
J:5417
|
foam cell reticulosis
|
J:275
|
sphingomyelinosis
|
J:5112
|
Fmc1em1Aitn/Fmc1+
(C57BL/6JJmsSlc-Fmc1em1Aitn)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:257586
|
decreased susceptibility to neuronal excitotoxicity
|
J:257586
|
Fmc1em1Aitn/Fmc1em1Aitn
(C57BL/6JJmsSlc-Fmc1em1Aitn)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:257586
|
Fmn1tm1Awb/Fmn1tm1Awb
(involves: 129S4/SvJae)
|
abnormal cell physiology
|
J:137209
|
Fmn2tm1Led/Fmn2tm1Led
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss))
|
abnormal oocyte morphology
|
J:81246
|
abnormal primary polar body morphology
|
J:81246
|
impaired polar body extrusion
|
J:81246
|
Fmnl1tm1.2Sdb/Fmnl1tm1.2Sdb Lyz2tm1(cre)Ifo/Lyz2tm1(cre)Ifo
(involves: C3H * C57BL/6 * FVB/N)
|
impaired macrophage chemotaxis
|
J:250144
|
Fmo5tm1Eshe/Fmo5tm1Eshe
(B6.129P2-Fmo5tm1Eshe)
|
decreased fatty acid oxidation
|
J:223365
|
increased fatty acid oxidation
|
J:223365
|
Fmr1tm1Cgr/Fmr1tm1Cgr
(involves: 129P2/OlaHsd)
|
abnormal neuron differentiation
|
J:159211
|
abnormal neuronal precursor proliferation
|
J:159211
|
Fmr1tm1Usdn/Y
(involves: 129S6/SvEvTac * C57BL/6 * FVB)
|
abnormal chromosome morphology
|
J:121413
|
Fmr1tm1Usdn/Fmr1tm1Usdn
(B6.129S6(Cg)-Fmr1tm1Usdn)
|
abnormal female germ cell morphology
|
J:196840
|
abnormal female meiosis
|
J:196840
|
Fn1tm1Ksek/Fn1tm1Ksek
(involves: 129P2/OlaHsd * 129/Sv)
|
abnormal extracellular matrix morphology
|
J:93250
|
decreased fibroblast proliferation
|
J:93250
|
Fn1tm1Ref/Fn1tm1Ref Tg(Mx1-cre)1Cgn/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
increased neuron apoptosis
|
J:67961
|
Fn1tm2.1Ref/Fn1tm2.1Ref
(involves: 129S1/Sv * 129X1/SvJ)
|
increased tail bud apoptosis
|
J:177821
|
Fn3ktm1Mvdc/Fn3ktm1Mvdc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:116037
|
Fndc3asys/Fndc3asys
(involves: C3H * FVB/N)
|
multinucleated giant male germ cells
|
J:10611
|
Fndc3btm1Maim/Fndc3btm1Maim
(B6.129S2-Fndc3btm1Maim)
|
abnormal cell adhesion
|
J:163660
|
abnormal cell differentiation
|
J:163660
|
decreased fibroblast cell migration
|
J:163660
|
decreased fibroblast proliferation
|
J:163660
|
Fndc3btm1Maim/Fndc3btm1Maim
(involves: 129S2/SvPas)
|
abnormal cell differentiation
|
J:162425
|
Fndc5em21Gpt/Fndc5em21Gpt
(C57BL/6JGpt-Fndc5em21Cd/Gpt)
|
abnormal fatty acid oxidation
|
J:247171
|
impaired autophagy
|
J:247171
|
Fnip1Gt(RRM154)Byg/Fnip1Gt(RRM154)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased B cell apoptosis
|
J:189078
|
Fnip1LPAB.1/Fnip1LPAB.1
(C57BL/6J-Fnip1LPAB.1)
|
increased B cell apoptosis
|
J:187318
|
Fnip1LPAB.1/Fnip1LPAB.1 Tg(IghMyc)22Bri/0
(involves: C57BL * C57BL/6J * SJL)
|
increased B cell apoptosis
|
J:187318
|
Fnip1m1Btlr/Fnip1m1Btlr
(C57BL/6J-Fnip1m1Btlr)
|
enhanced autophagy
|
J:234285
|
Fnip1tm1.1Baba/Fnip1tm1.1Baba Fnip2tm1.1Lss/Fnip2tm1.1Lss Tg(Cdh16-cre)91Igr/0
(involves: C57BL/6 * ICR)
|
abnormal mitochondrial physiology
|
J:220672
|
Fnip1tm1.1Baba/Fnip1tm1.1Baba Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6 * FVB)
|
abnormal mitochondrial physiology
|
J:220672
|
Fnip1tm1.2Baba/Fnip1tm1.2Baba
(involves: C57BL/6 * C57BL/6J * FVB/N * SJL)
|
increased B cell apoptosis
|
J:189078
|
Fntbtm1.1Bbd/Fntbtm1.1Bbd
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
decreased inner cell mass proliferation
|
J:98944
|
Fntbtm1.1Mbrg/Fntbtm1.1Mbrg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle
|
J:158937
|
abnormal cell morphology
|
J:158937
|
decreased fibroblast proliferation
|
J:158937
|
Fntbtm1.1Mbrg/Fntbtm1.1Mbrg Pggt1btm1Mbrg/Pggt1btm1Mbrg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased fibroblast apoptosis
|
J:158937
|
Fntbtm1.1Mbrg/Fntbtm1.1Mbrg Tg(KRT14-cre)1Amc/?
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased keratinocyte proliferation
|
J:158528
|
increased hair follicle apoptosis
|
J:158528
|
Fntbtm1.1Mbrg/Fntbtm1.2Mbrg
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * FVB/N)
|
abnormal cell cycle
|
J:158937
|
abnormal cell morphology
|
J:158937
|
decreased fibroblast proliferation
|
J:158937
|
Fntbtm1.1Mbrg/Fntbtm1.2Mbrg Krastm4Tyj/Kras+
(involves: 129P2/OlaHsd * 129S4/SvJae * BALB/cJ * C57BL/6 * FVB/N)
|
abnormal cell cycle
|
J:158937
|
Fntbtm1Bbd/Fntbtm1.1Bbd Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL)
|
decreased cell proliferation
|
J:98944
|
Fntbtm1Bbd/Fntbtm1Bbd Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL)
|
decreased cell proliferation
|
J:98944
|
Folr1tm1Fnn/Folr1tm1Fnn
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal neural crest cell migration
|
J:57765
|
Fostm1Wag/Fostm1Wag
(involves: 129S2/SvPas)
|
decreased retina apoptosis
|
J:65766
|
Fostm1Wag/Fostm1Wag
(involves: 129S2/SvPas * C57BL/6)
|
increased macrophage apoptosis
|
J:118693
|
Fostm1Wag/Fostm2(Fosl1)Wag
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6)
|
increased retina apoptosis
|
J:65766
|
Fostm2(Fosl1)Wag/Fostm2(Fosl1)Wag
(involves: 129P2/OlaHsd * C57BL/6)
|
increased retina apoptosis
|
J:65766
|
Fostm5.1Wag/Fostm5.1Wag
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal osteoclast differentiation
|
J:175064
|
Fostm6.1Wag/Fostm6.1Wag
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal osteoclast differentiation
|
J:175064
|
Fostm7Wag/Fostm7Wag Tg(Cd4-cre)1Cwi/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
decreased cell proliferation
|
J:190150
|
increased apoptosis
|
J:190150
|
Fosl1tm2Wag/Fosl1tm2Wag Meox2tm1(cre)Sor/Meox2+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6)
|
abnormal osteoblast physiology
|
J:93053
|
Fosl2tm2.1Wag/Fosl2tm2.1Wag
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:137646
|
Fosl2tm2Wag/Fosl2tm2Wag Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:137646
|
Fosl2tm2Wag/Fosl2tm2Wag Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
abnormal osteoblast physiology
|
J:211215
|
Foxa2tm1Dnl/Foxa2tm1Dnl
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell death
|
J:19896
|
abnormal neuron differentiation
|
J:19896
|
Foxa2tm1Jrt/Foxa2tm1Jrt
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
increased embryonic tissue cell apoptosis
|
J:50810
|
Foxa2tm1Jrt/Foxa2tm1Jrt
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:50810
|
Foxa3tm1Khk/Foxa3tm1Khk
(B6.129P2-Foxa3tm1Khk)
|
abnormal primordial germ cell proliferation
|
J:134427
|
increased adipocyte glucose uptake
|
J:216477
|
increased male germ cell apoptosis
|
J:134427
|
Foxb1tm1Pgr/Foxb1tm1Pgr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
maternal effect
|
J:44764
|
Foxc1hith/Foxc1hith
(involves: C57BL/6J * FVB/N)
|
abnormal basement membrane morphology
|
J:136459
|
abnormal radial glial cell morphology
|
J:136459
|
radial glial endfoot detachment
|
J:136459
|
Foxc1hith/Foxc1hith
(involves: C57BL/6J)
|
abnormal neuron differentiation
|
J:157301
|
abnormal neuron proliferation
|
J:157301
|
Foxc1hith/Foxc1tm1Blh
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal neuron differentiation
|
J:157301
|
abnormal neuron proliferation
|
J:157301
|
Foxc1tm1Blh/Foxc1tm1Blh
(involves: 129S6/SvEvTac * Black Swiss)
|
abnormal primordial germ cell migration
|
J:105944
|
decreased oocyte number
|
J:105944
|
oocyte degeneration
|
J:105944
|
patent ductus arteriosus
|
J:57677
|
Foxc1tm1Blh/Foxc1tm1Blh
(involves: 129S6/SvEvTac)
|
abnormal neuron differentiation
|
J:157301
|
abnormal neuron proliferation
|
J:157301
|
Foxc1tm1Tsku/Foxc1tm1Blh Tg(Tek-cre)1Rwng/0
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal cell migration
|
J:131323
|
Foxc2tm1Miu/Foxc2tm1Miu
(involves: 129P2/OlaHsd * C57BL/6J * ICR)
|
abnormal mesangial cell morphology
|
J:106710
|
Foxd3tm1.1Lby/Foxd3tm1.1Lby
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * CD-1))
|
abnormal cell proliferation
|
J:79491
|
Foxd3tm1Lby/Foxd3tm1Lby
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * CD-1))
|
abnormal anterior visceral endoderm cell migration
|
J:79491
|
abnormal cell proliferation
|
J:79491
|
decreased embryonic epiblast cell proliferation
|
J:79491
|
Foxd3tm2Lby/Foxd3tm2Lby
(involves: 129S6/SvEvTac)
|
abnormal cell proliferation
|
J:79491
|
Foxd3tm2Lby/Foxd3tm3Lby H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal cardiac neural crest cell migration
|
J:134482
|
abnormal enteric neural crest cell migration
|
J:134482
|
increased apoptosis
|
J:134482
|
increased hindbrain apoptosis
|
J:134482
|
Foxf1em1Vvk/Foxf1+
(involves: C57BL/6 * DBA/2)
|
decreased lung endothelial cell proliferation
|
J:296328
|
Foxg1tm1(cre)Skm/Foxg1+ Frs2tm1Fwan/Frs2tm1Fwan Frs3tm1Jheb/Frs3tm1Jheb
(involves: 129 * Swiss Webster)
|
cellular phenotype
|
J:242687
|
Foxg1tm1(cre)Skm/Foxg1+ Lrp2tm1Tew/Lrp2tm1Tew
(involves: 129P2/OlaHsd)
|
decreased cell proliferation
|
J:238249
|
increased retina apoptosis
|
J:238249
|
Foxg1tm1(tTA)Lai/Foxg1tm1M Tg(tetO-Foxg1)1Lai/0
(involves: 129S1/Sv * C57BL/6)
|
abnormal neuron differentiation
|
J:78115
|
Foxg1tm1Chzh/Foxg1tm1Chzh Tg(Fzd9-cre/ERT)1Chzh/0
(involves: C57BL/6 * FVB)
|
abnormal neuronal precursor proliferation
|
J:182692
|
abnormal radial glial cell morphology
|
J:182692
|
Foxg1tm1M/Foxg1tm1M
(involves: 129S1/Sv)
|
abnormal neuron differentiation
|
J:78115
|
abnormal neuronal precursor proliferation
|
J:78115
|
Foxi1tm1Sven/Foxi1tm1Sven
(involves: CD-1)
|
increased apoptosis
|
J:82307
|
Foxi1tm1Sven/Foxi1tm1Sven
(involves: 129S1/Sv * 129X1/SvJ)
|
impaired sperm migration in female genital tract
|
J:112876
|
kinked sperm flagellum
|
J:112876
|
Foxi3tm1.2Akg/Foxi3tm1.2Akg
(involves: 129X1/SvJ * BALB/c)
|
increased cranial neural crest cell apoptosis
|
J:207523
|
Foxi3tm1.2Akg/Foxi3tm1.2Akg
(involves: 129X1/SvJ)
|
increased embryonic tissue cell apoptosis
|
J:228880
|
Foxj1tm1.1Ctk/Foxj1tm1.2Ctk Tg(FOXJ1-cre/ERT2)1Blh/0
(involves: C57BL/6 * DBA)
|
abnormal neuron differentiation
|
J:174694
|
Foxj1tm1.1Ctk/Foxj1tm1.2Ctk Tg(FOXJ1-EGFP)85Leo/0 Tg(Nes-cre)1Kln/0
(involves: C3H * C57BL/6 * C57BL/6J * SJL)
|
abnormal neuron differentiation
|
J:174694
|
Foxj1tm1Bph/Foxj1tm1Bph
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss)
|
absent brain ependyma motile cilia
|
J:50025
|
absent oviduct epithelium motile cilium
|
J:50025
|
absent respiratory motile cilia
|
J:50025
|
absent sperm flagellum
|
J:50025
|
Foxj1tm1Slb/Foxj1tm1Slb
(involves: 129X1/SvJ)
|
abnormal embryonic cilium location or orientation
|
J:182741
|
absent brain ependyma motile cilia
|
J:73616
|
absent nodal flow
|
J:182741
|
absent oviduct epithelium motile cilium
|
J:73616
|
absent respiratory motile cilia
|
J:73616
|
decreased embryonic cilium length
|
J:182741
|
Foxj2tm1.1Mxc/Foxj2tm1.1Mxc Tg(Ddx4-cre)1Dcas/0
(involves: FVB)
|
abnormal chromosomal synapsis
|
J:301841
|
arrest of male meiosis
|
J:301841
|
Foxj3Gt(XL913)Byg/Foxj3Gt(XL913)Byg
(either: 129P2/OlaHsd-Foxj3Gt(XL913)Byg or B6.129P2-Foxj3 |
abnormal skeletal muscle satellite cell proliferation
|
J:157260
|
Foxk1tm1Djg/Foxk1tm1Djg
(involves: 129S4/SvJae)
|
abnormal cell cycle
|
J:81688
|
Foxk2tm1.1Sven/Foxk2tm1.1Sven
(B6.129P2-Foxk2tm1.1Sven)
|
decreased adipocyte glucose uptake
|
J:273343
|
Foxk2tm1.2Sven/Foxk2tm1.2Sven
(B6.Cg-Foxk2tm1.2Sven)
|
decreased cellular glucose uptake
|
J:273343
|
decreased skeletal muscle cell glucose uptake
|
J:273343
|
Foxl1tm1Khk/Foxl1tm1Khk
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:41235
|
Foxl2tm1Tre/Foxl2tm1Tre
(involves: 129P2/OlaHsd * Black Swiss * CD-1)
|
decreased granulosa cell proliferation
|
J:87737
|
impaired granulosa cell differentiation
|
J:87737
|
Foxl2tm2.1Tre/Foxl2tm2.1Tre Gnrhrtm1.1(cre)Uboe/Gnrhr+
(involves: 129S1/Sv * 129X1/SvJ)
|
arrest of male meiosis
|
J:204036
|
asthenozoospermia
|
J:204036
|
immotile sperm
|
J:204036
|
oligozoospermia
|
J:204036
|
Foxm1tm1.1Rhc/Foxm1tm1.1Rhc
(involves: 129X1/SvJ)
|
abnormal cell cycle
|
J:94883
|
Foxm1tm1.1Rhc/Foxm1tm1.1Rhc
(involves: 129X1/SvJ * C57BL/6)
|
decreased mesenchymal cell proliferation involved in lung development
|
J:100263
|
Foxm1tm1.1Rhc/Foxm1tm1.1Rhc
(B6.129X1-Foxm1tm1.1Rhc)
|
decreased fetal cardiomyocyte proliferation
|
J:119481
|
Foxm1tm1Rhc/Foxm1tm1Rhc Tg(Alb1-cre)1Khk/0
(involves: 129X1/SvJ * C57BL/6 * SJL)
|
abnormal cell cycle
|
J:94883
|
Foxm1tm1Rhc/Foxm1tm1Rhc Tg(Pdx1-cre)89.1Dam/0
(involves: 129X1/SvJ * C57BL/6 * CBA)
|
decreased pancreatic beta cell proliferation
|
J:111026
|
Foxn1nu/Foxn1nu
(Not Specified)
|
asthenozoospermia
|
J:5043
|
coiled sperm flagellum
|
J:5043
|
Foxn1nu/Foxn1nu
(involves: BALB/c)
|
chromosomal instability
|
J:40405
|
Foxn1nu/Foxn1tm1.1Dmsu Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129/Sv * C57BL/6 * CBA * SJL)
|
increased thymocyte apoptosis
|
J:159773
|
Foxn4tm1Xia/Foxn4tm1Xia
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased retina apoptosis
|
J:92622
|
Foxo1tm1.1Stlp/Foxo1tm1.1Stlp Tg(Lck-cre)1Cwi/0
(involves: 129S4/SvJae)
|
decreased T cell proliferation
|
J:154205
|
decreased thymocyte apoptosis
|
J:154205
|
Foxo1tm1Flv/Foxo1tm1Flv Foxp3tm4(YFP/icre)Ayr/Foxp3+
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ)
|
increased T cell proliferation
|
J:189962
|
Foxo1tm1Flv/Foxo1tm1Flv Tg(Cd4-cre)1Cwi/?
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2)
|
increased T cell proliferation
|
J:147057
|
Foxo1tm1Rdp/Foxo1tm1Rdp Foxo3tm1Rdp/Foxo3tm1Rdp Foxo4tm1Rdp/Foxo4tm1Rdp Tg(Ins2-cre)23Herr/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA/J)
|
abnormal mitochondrial physiology
|
J:215526
|
abnormal pancreatic beta cell differentiation
|
J:215526
|
Foxo3Gt(VICTR20)1Kca/Foxo3Gt(VICTR20)1Kca
(involves: 129S5/SvEvBrd * C57BL/6)
|
oocyte degeneration
|
J:88638
|
Foxo3Gt(XAO26)Byg/Foxo3Gt(XAO26)Byg
(involves: 129P2/OlaHsd)
|
increased T cell proliferation
|
J:93593
|
Foxo3mommeR1/Foxo3mommeR1 Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
(FVB/NJ-Foxo3mommeR1 Tg(HBA1-Gfp)1Ew)
|
abnormal oocyte morphology
|
J:170710
|
abnormal oogenesis
|
J:170710
|
abnormal polar body morphology
|
J:170710
|
Foxo3tm1.1Rdp/Foxo3tm1.1Rdp
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal oocyte morphology
|
J:84269
|
Foxo3tm1Nmt/Foxo3tm1Nmt
(B6.Cg-Foxo3tm1Nmt)
|
decreased apoptosis
|
J:123409
|
Foxo6tm1(KOMP)Vlcg/Foxo6tm1(KOMP)Vlcg
(B6J.B6NTac-Foxo6tm1(KOMP)Vlcg)
|
impaired macrophage chemotaxis
|
J:236585
|
Foxp1tm1.1Pwt/Foxp1tm1.1Pwt Tg(Cd4-cre)1Cwi/0
(involves: 129 * C57BL/6 * DBA/2)
|
increased T cell apoptosis
|
J:156832
|
Foxp1tm1Eem/Foxp1+ Foxp2tm1Bux/Foxp2tm1Bux
(involves: 129X1/SvJ * C57BL/6)
|
decreased mesenchymal cell proliferation involved in lung development
|
J:121421
|
Foxp1tm2.1Eem/Foxp1tm2.1Eem Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129 * C57BL/6 * SJL)
|
increased fetal cardiomyocyte proliferation
|
J:163662
|
Foxp1tm2.1Eem/Foxp1tm2.1Eem Tg(Tek-cre)1Ywa/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal fetal cardiomyocyte proliferation
|
J:163662
|
Foxp2tm1Bux/Foxp2+
(involves: C57BL/6)
|
abnormal radial glial cell morphology
|
J:99864
|
Foxp2tm1Bux/Foxp2tm1Bux
(involves: C57BL/6)
|
abnormal radial glial cell morphology
|
J:99864
|
Foxp3m1Btlr/Y
(C57BL/6J-Foxp3m1Btlr)
|
azoospermia
|
J:141212
|
Foxp3tm3Tch/Y
(C.129X1-Foxp3tm3Tch)
|
increased T cell proliferation
|
J:120636
|
Foxp3tm3Tch/Foxp3+
(C.129X1-Foxp3tm3Tch)
|
increased T cell apoptosis
|
J:120636
|
Fpr1tm1Gao/Fpr1tm1Gao
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:53354
|
Fpr2tm1.2Jimw/Fpr2tm1.2Jimw
(B6.129X1-Fpr2tm1.2Jimw)
|
impaired macrophage chemotaxis
|
J:160074
|
impaired neutrophil chemotaxis
|
J:160074
|
Fpr2tm1.2Jimw/Fpr2tm1.2Jimw
(involves: 129X1/SvJ)
|
abnormal dendritic cell chemotaxis
|
J:199611
|
abnormal enterocyte proliferation
|
J:197568
|
Fpr2tm1Rjf/Fpr2tm1Rjf
(involves: 129S/SvEv * C57BL/6)
|
impaired macrophage chemotaxis
|
J:159658
|
fpw/fpw
(involves: C3H/HeJ * C57BL/6J)
|
abnormal spermatogonia proliferation
|
J:151726
|
decreased cell proliferation
|
J:151726
|
decreased hepatocyte proliferation
|
J:151726
|
increased cell proliferation
|
J:151726
|
Fras1bl/Fras1bl
(involves: 101/H * C3H/HeH)
|
abnormal basement membrane morphology
|
J:83745
|
increased metanephric mesenchyme apoptosis
|
J:83745
|
Fras1rdf/Fras1rdf
(involves: C57BL/6J * FVB/NJ)
|
abnormal interdigital cell death
|
J:231083
|
Fras1tm1Chpk/Fras1tm1Chpk
(involves: 129S1/Sv * 129X1/SvJ * NMRI)
|
abnormal basement membrane morphology
|
J:137010
|
Frmd3em1Zhaj/Frmd3em1Zhaj Tg(MMTV-PyVT)634Mul/0
(B6.Cg-Frmd3em1Zhaj Tg(MMTV-PyVT)634Mul)
|
increased mammary gland epithelial cell proliferation
|
J:350496
|
FrylGt(Ayu21-T312)Imeg/FrylGt(Ayu21-T312)Imeg
(B6J.Cg-FrylGt(Ayu21-T312)Imeg)
|
increased kidney apoptosis
|
J:260667
|
Fscn1Gt(OST124903)Lex/Fscn1Gt(OST124903)Lex
(B6.129S5-Fscn1Gt(OST124903)Lex)
|
abnormal cell cycle
|
J:197025
|
abnormal dendritic cell chemotaxis
|
J:169408
|
abnormal fibroblast physiology
|
J:205179
|
Fscn1Gt(OST124903)Lex/Fscn1Gt(OST124903)Lex Tg(CAG-Bgeo/GFP)21Lbe/0 Tg(Tyr-cre)1Lru/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal melanoblast migration
|
J:197025
|
Fscn1Gt(OST124903)Lex/Fscn1Gt(OST124903)Lex Tg(Dct-lacZ)A12Jkn/0
(involves: C57BL/6 * CBA)
|
abnormal melanoblast migration
|
J:197025
|
Fshbtm1Zuk/Fshbtm1Zuk
(either: 129S/SvEv or (involves: 129S7/SvEvBrd * C57BL/6))
|
asthenozoospermia
|
J:38099
|
oligozoospermia
|
J:38099
|
Fshbtm1Zuk/Fshbtm1Zuk
(involves: 129S7/SvEvBrd)
|
decreased male germ cell number
|
J:71932
|
decreased round spermatid number
|
J:71932
|
decreased spermatogonia number
|
J:71932
|
Fshrtm1Saco/Fshr+
(involves: C57BL/6)
|
abnormal male germ cell morphology
|
J:61957
|
Fshrtm1Saco/Fshr+
(involves: 129)
|
abnormal female germ cell morphology
|
J:140008
|
absent oocytes
|
J:140008
|
increased apoptosis
|
J:140008
|
oocyte degeneration
|
J:140008
|
Fshrtm1Saco/Fshrtm1Saco
(involves: C57BL/6)
|
abnormal sperm flagellum morphology
|
J:61957,
J:50933
|
abnormal spermatogonia morphology
|
J:61957
|
asthenozoospermia
|
J:61957,
J:50933
|
decreased elongated spermatid number
|
J:61957
|
decreased spermatid number
|
J:61957
|
enlarged sperm head
|
J:61957
|
kinked sperm flagellum
|
J:61957
|
oligozoospermia
|
J:50933
|
Fshrtm1Saco/Fshrtm1Saco
(involves: 129)
|
abnormal sperm axoneme morphology
|
J:137005
|
abnormal sperm head morphology
|
J:137005
|
abnormal sperm nucleus morphology
|
J:137005
|
abnormal spermatid morphology
|
J:70680
|
abnormal spermatogonia proliferation
|
J:70680
|
asthenozoospermia
|
J:137005
|
decreased elongated spermatid number
|
J:70680
|
decreased round spermatid number
|
J:70680
|
detached acrosome
|
J:137005
|
oligozoospermia
|
J:137005
|
teratozoospermia
|
J:137005
|
Fsip1em1Nali/Fsip1em1Nali
(C57BL/6J-Fsip1em1Nali)
|
abnormal sperm flagellum morphology
|
J:333257
|
abnormal sperm head morphology
|
J:333257
|
abnormal sperm midpiece morphology
|
J:333257
|
abnormal spermatid morphology
|
J:333257
|
decreased sperm progressive motility
|
J:333257
|
decreased spermatid number
|
J:333257
|
globozoospermia
|
J:333257
|
oligozoospermia
|
J:333257
|
teratozoospermia
|
J:333257
|
Fsip2em1Nali/Fsip2em1Nali
(C57BL/6-Fsip2em1Nali)
|
abnormal sperm flagellum morphology
|
J:307606
|
absent sperm fibrous sheath
|
J:307606
|
decreased activated sperm motility
|
J:307606
|
oligozoospermia
|
J:307606
|
short sperm flagellum
|
J:307606
|
Fsttm1Zuk/Fsttm1Zuk
(B6.129S7-Fsttm1Zuk)
|
abnormal neuron differentiation
|
J:81451
|
Fstl1tm1Ajn/Fstl1tm1Ajn
(B6.Cg-Fstl1tm1Ajn)
|
increased lung apoptosis
|
J:322116
|
Fth1tm1Kjt/Fth1+
(involves: 129S/SvEvBrd * C57BL/6)
|
oxidative stress
|
J:158718
|
Fth1tm1Lck/Fth1tm1Lck
(involves: 129/Sv * C57BL/6 * FVB/N)
|
abnormal cell physiology
|
J:166515
|
abnormal mitochondrial physiology
|
J:166515
|
increased sensitivity to induced cell death
|
J:166515
|
Fts/Fts
(involves: C3H * C57BL/6 * SJL)
|
decreased germ cell number
|
J:168037
|
decreased primordial germ cell proliferation
|
J:168037
|
Fts/Fts+
(involves: C57BL/6 * SJL)
|
absent interdigital cell death
|
J:20159
|
Ftxtm1.1Oka/Ftxtm1.1Oka
(C57BL/6N-Ftxtm1.1Oka)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:268562
|
Fuca1tm1Tlub/Fuca1tm1Tlub
(involves: 129S2/SvPas * C57BL/6)
|
abnormal lysosome morphology
|
J:235359
|
fuddle/fuddle Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw
(involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal axon extension
|
J:168258
|
Fundc2tm1Qim/Fundc2tm1Qim
(involves: C57BL/6)
|
increased apoptosis
|
J:301633
|
Furintm1Jwmc/Furintm1Jwmc Tg(Gdf9-icre)5092Coo/0
(involves: 129P2/OlaHsd * C57BL/6J * CBA/J)
|
decreased granulosa cell proliferation
|
J:272231
|
Furintm1Jwmc/Furintm1Jwmc Tg(Zp3-cre)3Mrt/0
(involves: 129P2/OlaHsd * C57BL/6J * CBA/J)
|
abnormal meiotic spindle morphology
|
J:272231
|
abnormal oocyte morphology
|
J:272231
|
abnormal primary polar body morphology
|
J:272231
|
decreased granulosa cell proliferation
|
J:272231
|
increased granulosa cell apoptosis
|
J:272231
|
FusGt(U3NeoSV1)HO14Ggh/FusGt(U3NeoSV1)HO14Ggh
(B6.129S2-FusGt(U3NeoSV1)HO14Ggh)
|
abnormal chromosome morphology
|
J:60213
|
aneuploidy
|
J:60213
|
chromosome breakage
|
J:60213
|
Fustm1(DDIT3)Dron/Fustm1(DDIT3)Dron
(involves: 129S6/SvEvTac * CD-1)
|
abnormal male meiosis
|
J:60224
|
Fut4tm1Jbl/Fut4tm1Jbl
(B6.129S2-Fut4tm1Jbl)
|
impaired leukocyte tethering or rolling
|
J:79397
|
Fut4tm1Jbl/Fut4tm1Jbl Fut7tm1Jbl/Fut7tm1Jbl
(B6.129S2-Fut7tm1Jbl Fut4tm1Jbl)
|
abnormal leukocyte migration
|
J:79397
|
impaired leukocyte tethering or rolling
|
J:79397
|
Fut7tm1Jbl/Fut7tm1Jbl
(involves: 129S2/SvPas * C57BL/6J * DBA/2J)
|
abnormal leukocyte adhesion
|
J:35023
|
abnormal leukocyte migration
|
J:35023
|
abnormal leukocyte tethering or rolling
|
J:35023
|
FuzGt(AN0439)Wtsi/FuzGt(AN0439)Wtsi
(involves: 129P2/OlaHsd * C3H)
|
abnormal primary cilium morphology
|
J:154370
|
Fxnem8Lutzy/Fxnem8Lutzy
(C57BL/6J-Fxnem8Lutzy)
|
abnormal cell cycle
|
J:299300
|
abnormal mitochondrial chromosome morphology
|
J:299300
|
abnormal mitochondrial physiology
|
J:299300
|
decreased fibroblast proliferation
|
J:299300
|
decreased mitochondrial size
|
J:299300
|
early cellular replicative senescence
|
J:299300
|
increased mitochondrial number
|
J:299300
|
Fxntm1.1Pand/Fxntm1Mkn
(B6.Cg-Fxntm1.1Pand Fxntm1Mkn/J)
|
abnormal mitochondrial biogenesis
|
J:242978
|
Fxntm1Mkn/Fxntm1Mkn
(involves: 129 * C57BL/6J)
|
increased embryonic tissue cell apoptosis
|
J:62185
|
Fxntm1Mkn/Fxntm1Mkn Tg(FXN)YG8Pook/0
(involves: 129/Sv * C57BL/6 * CBA)
|
abnormal respiratory electron transport chain
|
J:114840
|
oxidative stress
|
J:114840
|
Fxntm1Mkn/Fxntm1Mkn Tg(FXN)YG22Pook/0
(involves: 129/Sv * C57BL/6 * CBA)
|
oxidative stress
|
J:114840
|
Fxntm2Mkn/Fxntm2.1Mkn Tg(Ckmm-cre)1Lrsn/0
(involves: 129 * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:90401
|
abnormal myocardial fiber mitochondrial morphology
|
J:75420
|
abnormal respiratory electron transport chain
|
J:75420,
J:90401
|
increased mitochondrial fission
|
J:75420
|
Fxntm2Mkn/Fxntm2.1Mkn Tg(Eno2-cre)39Jme/0
(involves: 129 * C57BL/6J)
|
dilated mitochondrion
|
J:75420
|
Fyb1tm1Gak/Fyb1tm1Gak
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal leukocyte adhesion
|
J:111368
|
decreased T cell proliferation
|
J:111368,
J:126545
|
Fyco1tm1.1Arte/Fyco1tm1.1Arte Tg(CAG-RFP/EGFP/Map1lc3b)1Hill/0 Tg(Prm-cre)58Og/0
(involves: 129S/Sv * C57BL/6J * C57BL/6N * C57BL/6NTac)
|
impaired autophagy
|
J:336796
|
Fyco1tm1.1Arte/Fyco1tm1.1Arte Tg(Prm-cre)58Og/0
(involves: 129S1/SvImJ * 129S4/SvJae * C57BL/6J * C57BL/6NTac)
|
abnormal endoplasmic reticulum morphology
|
J:336796
|
abnormal Golgi apparatus morphology
|
J:336796
|
impaired autophagy
|
J:336796
|
Fyco1tm1.2Arte/Fyco1tm1.2Arte
(involves: C57BL/6J * C57BL/6N * C57BL/6NTac * FVB/N)
|
abnormal endoplasmic reticulum morphology
|
J:336796
|
abnormal Golgi apparatus morphology
|
J:336796
|
impaired autophagy
|
J:336796
|
Fyco1tm1.2Arte/Fyco1tm1.2Arte Tg(CAG-RFP/EGFP/Map1lc3b)1Hill/0
(involves: C57BL/6J * C57BL/6N * C57BL/6NTac * FVB/N)
|
impaired autophagy
|
J:336796
|
Fyntm1Rmp/Fyntm1Rmp
(involves: 129S2/SvPas * C57BL/6)
|
decreased T cell proliferation
|
J:70886
|
Fyntm1Sor/Fyntm1Sor
(either: 129S7/SvEvBrd-Fyntm1Sor or (involves: 129S7/SvEvBrd * C57BL/6J))
|
decreased T cell proliferation
|
J:2242
|
Fyntm1Sor/Fyntm1Sor
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal sperm connecting piece morphology
|
J:185783
|
abnormal sperm head morphology
|
J:185783
|
abnormal sperm motility
|
J:185783
|
oligozoospermia
|
J:185783
|
teratozoospermia
|
J:185783
|
Fyntm1Sor/Fyntm1Sor
(B6.129S7-Fyntm1Sor)
|
abnormal T cell proliferation
|
J:93886
|
Fyntm1Sor/Fyntm1Sor Lcktm1Litt/Lcktm1.1Litt Tnfrsf4tm2(cre)Nik/Tnfrsf4+
(involves: 129S7/SvEvBrd * 129X1/SvJ)
|
decreased T cell proliferation
|
J:152472
|
Fyntm1Yik/Fyntm1Yik
(involves: C57BL/6 * CBA)
|
oligozoospermia
|
J:74017
|
Fzd3tm1(FZD3)Lex/Fzd3tm1(FZD3)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
cellular phenotype
|
J:185566
|
Fzd3tm1Nat/Fzd3+ Fzd6tm1Nat/Fzd6tm1Nat
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
oligozoospermia
|
J:105752
|
Fzd4tm1Nat/Fzd4tm1Nat
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
impaired luteal cell differentiation
|
J:115734
|
Fzd5tm1Mmt/Fzd5tm1Cle Tg(Six3-cre)69Frty/0
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal retina apoptosis
|
J:142601
|
abnormal vascular regression
|
J:142601
|
Fzd5tm1Mmt/Fzd5tm1Mmt
(involves: 129X1/SvJ)
|
increased retina apoptosis
|
J:136314
|
Fzd9tm1Uta/Fzd9tm1Uta
(involves: 129X1/SvJ)
|
decreased osteoblast proliferation
|
J:169924
|
impaired osteoblast differentiation
|
J:169924
|
Fzr1Gt(3003)Tgen/Fzr1Gt(3003)Tgen
(involves: C57BL/6 * CBA)
|
decreased fibroblast cell migration
|
J:162785
|
Fzr1Gt(RRJ067)Byg/Fzr1Gt(RRJ067)Byg
(involves: 129P2/OlaHsd)
|
abnormal mitosis
|
J:138545
|
binucleate
|
J:138545
|
decreased cell proliferation
|
J:138545
|
Fzr1tm1.1Mama/Fzr1tm1.1Mama
(involves: BALB/cJ * C57BL/6 * SJL)
|
decreased cell proliferation
|
J:137456
|
G0s2tm1(KOMP)Vlcg/G0s2tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal fat cell differentiation
|
J:232077
|
maternal effect
|
J:225236
|
G2e3Gt(RRM192)Byg/G2e3Gt(RRM192)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased apoptosis
|
J:139062
|
G3bp1tm1Tazi/G3bp1+
(involves: 129S2/SvPas)
|
maternal effect
|
J:101358
|
G3bp1tm1Tazi/G3bp1tm1Tazi
(involves: 129S2/SvPas)
|
decreased cell proliferation
|
J:101358
|
increased neuron apoptosis
|
J:101358
|
G3bp2em1Smoc/G3bp2em1.1Smoc Tg(Ddx4-cre)1Dcas/0
(B6.Cg-G3bp2em1Smoc/G3bp2em1.1Smoc Tg(Ddx4-cre)1Dcas)
|
increased male germ cell apoptosis
|
J:327036
|
G3bp2em1Smoc/G3bp2em1.1Smoc Tg(Stra8-icre)1Reb/0
(B6.Cg-G3bp2em1Smoc/G3bp2em1.1Smoc Tg(Stra8-icre)1Reb)
|
increased male germ cell apoptosis
|
J:327036
|
G6pc2tm1.1Pesa/G6pc2tm1.1Pesa
(NOD.129S2-G6pc2tm1.1Pesa)
|
decreased T cell proliferation
|
J:160286
|
G6pdxa-m1Neu/Y
(involves: 102/El * C3H/El * T-stock)
|
abnormal redox activity
|
J:95754
|
G6pdxtm1Luz/Y
(involves: 129S1/Sv * C57BL/6J)
|
increased allantois apoptosis
|
J:78546
|
increased embryonic tissue cell apoptosis
|
J:78546
|
G6pdxtm1Luz/G6pdx+
(involves: 129S1/Sv * C57BL/6J)
|
increased allantois apoptosis
|
J:78546
|
increased embryonic tissue cell apoptosis
|
J:78546
|
paternal imprinting
|
J:78546
|
Gaatm1Rabn/Gaatm1Rabn
(involves: 129X1/SvJ * C57BL/6)
|
abnormal lysosome morphology
|
J:48839
|
Gaatm1Rabn/Gaatm1Rabn Tg(CMV-GAA*P545L)#Kjv/0
(involves: 129X1/SvJ * C57BL/6)
|
abnormal lysosome physiology
|
J:219022
|
Gab1tm1Wbm/Gab1tm1Wbm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal muscle precursor cell migration
|
J:68751
|
Gab1tm1Wbm/Gab1tm1Wbm
(involves: 129P2/OlaHsd)
|
abnormal muscle precursor cell migration
|
J:100909
|
Gab1tm5Wbm/Gab1tm5Wbm
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * CD-1)
|
abnormal cell migration
|
J:125303
|
Gab2tm1Hhg/Gab2tm1Hhg
(involves: 129S4/SvJae)
|
decreased mast cell degranulation
|
J:70424
|
Gab2tm1Pngr/Gab2tm1Pngr
(B6.Cg-Gab2tm1Pngr)
|
abnormal osteoclast differentiation
|
J:97515
|
Gab2tm1Thir/Gab2tm1Thir
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal mast cell differentiation
|
J:75092
|
Gab2tm3.1Thir/Gab2tm3.1Thir
(involves: 129T/SvJcl * C57BL/6Jcl)
|
decreased mast cell degranulation
|
J:178045
|
Gab2tm4.1Thir/Gab2tm4.1Thir
(involves: 129T/SvJcl * C57BL/6Jcl)
|
decreased mast cell degranulation
|
J:178045
|
Gabpatm1Agro/Gabpatm1Agro
(involves: 129)
|
abnormal cell cycle checkpoint function
|
J:126422
|
decreased DNA replication
|
J:126422
|
decreased fibroblast proliferation
|
J:126422
|
increased cell mass
|
J:126422
|
Gabpb2Gt(RRJ488)Byg/Gabpb2Gt(RRJ488)Byg
(involves: 129P2/OlaHsd)
|
increased B cell proliferation
|
J:141846
|
Gad1tm1.1Tama/Gad1+ Pcntm239Asp/Pcntm239Asp
(involves: C57BL/6 * C57BL/6J * CBA * FVB/N)
|
abnormal neuronal migration
|
J:158418
|
abnormal neuronal precursor proliferation
|
J:158418
|
increased apoptosis
|
J:158418
|
Gad1tm1Tama/? Lhx6tm2Vpa/Lhx6tm2Vpa
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * CBA)
|
abnormal neuronal migration
|
J:119476
|
Gadd45atm1Ajf/Gadd45atm1Ajf
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129X1/SvJ * C57BL/6))
|
abnormal cell nucleus morphology
|
J:57882
|
abnormal cell physiology
|
J:57882
|
abnormal centrosome morphology
|
J:57882
|
abnormal chromosome morphology
|
J:57882
|
abnormal chromosome number
|
J:57882
|
abnormal mitosis
|
J:57882
|
aneuploidy
|
J:57882
|
decreased mitotic index
|
J:57882
|
increased fibroblast proliferation
|
J:57882
|
increased kidney cell proliferation
|
J:76041
|
increased mesangial cell number
|
J:76041
|
increased T cell proliferation
|
J:76041
|
mesangial cell interposition
|
J:76041
|
Gadd45atm1Ajf/Gadd45atm1Ajf
(involves: 129)
|
abnormal base-excision repair
|
J:101710
|
Gadd45atm1Ajf/Gadd45atm1Ajf Gadd45btm1Daa/Gadd45btm1Daa Gadd45gtm1Mhol/Gadd45gtm1Mhol
(either: (involves: 129X1/SvJ) or (involves: 129P2/OlaHsd * 129X1/SvJ))
|
increased cell proliferation
|
J:110650
|
Gadd45btm1Flv/Gadd45btm1Flv
(B6.129S6-Gadd45btm1Flv)
|
increased T cell proliferation
|
J:118837
|
Gadd45gtm1Mhol/Gadd45gtm1Mhol
(involves: 129)
|
abnormal cell physiology
|
J:110650
|
Gadd45gip1tm1Kong/Gadd45gip1tm1Kong
(involves: 129P2/OlaHsd * C57BL/6)
|
absent inner cell mass proliferation
|
J:156583
|
decreased cell proliferation
|
J:156583
|
increased embryonic tissue cell apoptosis
|
J:156583
|
Gadd45gip1tm1Kong/Gadd45gip1tm2Kong
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:156583
|
Gadd45gip1tm2Kong/Gadd45gip1tm2Kong Tg(Ins2-cre)25Mgn/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA)
|
abnormal mitochondrial crista morphology
|
J:220742
|
abnormal mitochondrial matrix morphology
|
J:220742
|
abnormal mitochondrial morphology
|
J:220742
|
abnormal mitochondrial physiology
|
J:220742
|
decreased pancreatic beta cell proliferation
|
J:220742
|
increased mitochondrial number
|
J:220742
|
Gadd45gip1tm2Kong/Gadd45gip1tm2Kong Tg(Vil1-cre)997Gum/0
(involves: 129P2/OlaHsd * C57BL/6J * SJL)
|
abnormal small intestinal crypt cell proliferation
|
J:156319
|
Gaktm1Noj/Gaktm1Noj
(C57BL/6-Gaktm1Noj)
|
cellular phenotype
|
J:179585
|
Gaktm2Legr/Gaktm2Legr
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal plasma membrane morphology
|
J:180119
|
Gaktm2Legr/Gaktm2Legr Tg(Nes-cre)1Kln/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:180119
|
abnormal neuronal precursor proliferation
|
J:180119
|
Gal3st1tm1Kho/Gal3st1tm1Kho
(involves: 129P2/OlaHsd)
|
arrest of male meiosis
|
J:78560
|
azoospermia
|
J:78560
|
increased male germ cell apoptosis
|
J:78560
|
multinucleated giant male germ cells
|
J:78560
|
Galtm1Wyn/Galtm1Wyn
(129P2-Galtm1Wyn)
|
increased susceptibility to neuronal excitotoxicity
|
J:89287
|
Galctwi/Galctwi
(B6.CE-Galctwi/J)
|
increased oligodendrocyte progenitor number
|
J:170081
|
Galctwi/Galctwi
(involves: CE/J)
|
abnormal glial cell apoptosis
|
J:57215
|
Galctwi/Galctwi Hpgdstm1Urad/Hpgdstm1Urad
(B6.Cg-Hpgdstm1Urad Galctwi)
|
decreased apoptosis
|
J:108359
|
Galnstm1Toma/Galnstm1Toma
(involves: 129X1/SvJ * C57BL/6)
|
abnormal lysosome physiology
|
J:87155
|
Galnstm2(GALNS)Toma/Galnstm2(GALNS)Toma
(involves: 129X1/SvJ * C57BL/6)
|
lysosomal protein accumulation
|
J:104126
|
Galnstm2(GALNS)Toma/Galnstm2(GALNS)Toma
(involves: 129X1/SvJ * C57BL/6J)
|
lysosomal protein accumulation
|
J:122458
|
Galnstm3Toma/Galnstm3Toma
(involves: 129X1/SvJ * C57BL/6J)
|
lysosomal protein accumulation
|
J:122458
|
Galnt1tm1.1Jxm/Galnt1tm1.1Jxm
(B6NHsd.Cg-Galnt1tm1.1Jxm)
|
impaired leukocyte tethering or rolling
|
J:128982
|
increased cell proliferation
|
J:242253
|
Galnt3tcal/Galnt3tcal
(involves: C3H * C57BL/6J)
|
increased kidney apoptosis
|
J:187064
|
increased testis apoptosis
|
J:187064
|
oligozoospermia
|
J:187064
|
Galnt3tm1Mjec/Galnt3tm1Mjec
(involves: 129S/SvEv * C57BL/6J)
|
oligozoospermia
|
J:151805
|
teratozoospermia
|
J:151805
|
Galnt3tm1Tok/Galnt3tm1Tok
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal acrosome assembly
|
J:301856
|
abnormal proacrosomal vesicle fusion
|
J:301856
|
abnormal sperm head morphology
|
J:301856
|
abnormal sperm mitochondrial sheath morphology
|
J:301856
|
abnormal sperm nucleus morphology
|
J:301856
|
abnormal spermatid morphology
|
J:301856
|
asthenozoospermia
|
J:301856
|
globozoospermia
|
J:301856
|
immotile sperm
|
J:301856
|
increased male germ cell apoptosis
|
J:301856
|
oligozoospermia
|
J:301856
|
teratozoospermia
|
J:301856
|
Galntl5tm1Nari/Galntl5+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal acrosome morphology
|
J:206466
|
asthenozoospermia
|
J:206466
|
oligozoospermia
|
J:206466
|
teratozoospermia
|
J:206466
|
GaltGt(E285B04)Wrst/GaltGt(E285B04)Wrst
(involves: 129P2/OlaHsd * C57BL/6J)
|
oxidative stress
|
J:234753
|
Gamttm1Isb/Gamttm1Isb
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:90367
|
multinucleated giant male germ cells
|
J:90367
|
oligozoospermia
|
J:90367
|
Gantm1Yany/Gantm1Yany
(Not Specified)
|
abnormal cell morphology
|
J:103926
|
Gap43tm1Kmr/Gap43tm1Kmr
(129/Sv-Gap43tm1Kmr)
|
abnormal axon extension
|
J:56646
|
abnormal axon guidance
|
J:56646
|
Gap43tm1Kmr/Gap43tm1Kmr
(B6.129S1-Gap43tm1Kmr)
|
abnormal axon extension
|
J:56646
|
abnormal axon guidance
|
J:56646
|
abnormal neuronal precursor proliferation
|
J:126908
|
Gapdhstm1Dao/Gapdhstm1Dao
(involves: 129S6/SvEvTac * C57BL/6N)
|
asthenozoospermia
|
J:94734
|
Gapttm1.1Wz/Gapttm1.1Wz
(Not Specified)
|
increased B cell proliferation
|
J:138146
|
Garin1aem1Osb/Garin1aem1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal acrosome morphology
|
J:314135
|
abnormal sperm head morphology
|
J:314135
|
Garin1bem1Osb/Garin1bem1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal acrosome morphology
|
J:314135
|
abnormal sperm head morphology
|
J:314135
|
decreased activated sperm motility
|
J:314135
|
Garin2em1Osb/Garin2em1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal sperm head morphology
|
J:350937
|
asthenozoospermia
|
J:350937
|
Garin3em1Osb/Garin3em1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal acrosome morphology
|
J:350937
|
abnormal sperm head morphology
|
J:350937
|
asthenozoospermia
|
J:350937
|
Garin4em1Osb/Garin4em1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal sperm head morphology
|
J:350937
|
Garin5aem1Osb/Garin5aem1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal sperm head morphology
|
J:350937
|
asthenozoospermia
|
J:350937
|
Garin5bem1Osb/Garin5bem1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal sperm head morphology
|
J:350937
|
asthenozoospermia
|
J:350937
|
Gas2tm1(GFP/cre/ERT2)Pzg/Gas2tm1(GFP/cre/ERT2)Pzg
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal basal lamina morphology
|
J:251841
|
Gas2l3tm1c(EUCOMM)Hmgu/Gas2l3tm1c(EUCOMM)Hmgu Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N)
|
abnormal fetal cardiomyocyte proliferation
|
J:244087
|
abnormal mitotic cytokinesis
|
J:244087
|
Gas2l3tm1c(EUCOMM)Hmgu/Gas2l3tm1c(EUCOMM)Hmgu Nkx2-5tm2(cre)Rph/Nkx2-5+
(involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6N)
|
cardiac interstitial fibrosis
|
J:244087
|
Gas2l3tm1d(EUCOMM)Hmgu/Gas2l3tm1d(EUCOMM)Hmgu
(involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N)
|
abnormal fetal cardiomyocyte proliferation
|
J:244087
|
cardiac interstitial fibrosis
|
J:244087
|
Gas5em1Gpt/Gas5+
(C57BL/6JGpt-Gas5em1Gpt/Gpt)
|
impaired osteoblast differentiation
|
J:298688
|
Gas6tm1Hiar/Gas6tm1Hiar
(B6.129P2-Gas6tm1Hiar)
|
decreased kidney cell proliferation
|
J:112430
|
Gas8Gt(CH0760)Wtsi/Gas8Gt(CH0760)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal brain ependyma motile cilium physiology
|
J:234173
|
abnormal respiratory motile cilium physiology
|
J:234173
|
Gata1Plt13/Gata1+
(BALB/c-Gata1Plt13)
|
polyploidy
|
J:113720
|
Gata1tm1Mym/Y Tg(Gata1*V205G)1Mym/0
(involves: C57BL/6 * DBA/2)
|
abnormal megakaryocyte differentiation
|
J:89054
|
Gata1tm2.1Sho/Y
(involves: 129S4/SvJae * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:41605
|
Gata1tm2.1Sho/Gata1+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:41605
|
Gata1tm2Sho/Y
(involves: 129S4/SvJae * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:41605
|
Gata1tm2Sho/Gata1+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:41605
|
Gata1tm4Sho/Y
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:77724
|
Gata3tm1.1Gan/Gata3tm1.1Gan Tg(Pax2-cre)1Akg/0
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6Ncr)
|
increased apoptosis
|
J:199588
|
Gata3tm1Gsv/Gata3+
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6))
|
abnormal axon guidance
|
J:66227
|
Gata3tm1Gsv/Gata3tm1Gsv
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6))
|
abnormal axon guidance
|
J:66227
|
Gata3tm1Gsv/Gata3tm1Gsv
(involves: 129 * FVB)
|
abnormal neural crest cell migration
|
J:310312
|
Gata3tm1Iho/Gata3tm1Iho Tg(Lck-cre)1Cwi/0
(involves: BALB/c)
|
increased T cell apoptosis
|
J:86996
|
Gata3tm2Gsv/Gata3+
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6))
|
abnormal axon guidance
|
J:66227
|
Gata3tm2Gsv/Gata3tm2Gsv
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S7/SvEvBrd * C57BL/6))
|
abnormal axon guidance
|
J:66227
|
Gata4tm1(cre)Svs/Gata4+ Tg(Sox3-GFP,Tyr)HolNpln/Tg(Sox3-GFP,Tyr)HolNpln
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal enteric neural crest cell migration
|
J:229828
|
Gata4tm1.1Sad/Gata4tm1.1Sad Amhr2tm3(cre)Bhr/Amhr2+
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6J)
|
asthenozoospermia
|
J:169018
|
decreased elongated spermatid number
|
J:169018
|
decreased male germ cell number
|
J:169018
|
decreased sperm progressive motility
|
J:169018
|
increased male germ cell apoptosis
|
J:169018
|
multinucleated giant male germ cells
|
J:169018
|
oligozoospermia
|
J:169018
|
Gata4tm1.1Sad/Gata4tm1.1Sad Gata6tm2.1Sad/Gata6tm2.1Sad Tg(Wt1-cre)1Jbeb/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
decreased fetal cardiomyocyte proliferation
|
J:206877
|
Gata4tm1.1Sad/Gata4tm1.1Sad Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
increased cardiomyocyte apoptosis
|
J:121367
|
Gata4tm1.1Sad/Gata4tm1.1Sad Tg(Myh7-cre)1Jmk/0
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
increased cardiomyocyte apoptosis
|
J:121367
|
Gata4tm1.1Wtp/Gata4tm1.1Wtp Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129S7/SvEvBrd)
|
abnormal fetal cardiomyocyte proliferation
|
J:99203
|
Gata4tm1.1Wtp/Gata4tm1.1Wtp Tg(Myh6-cre)2182Mds/0
(involves: FVB/N)
|
abnormal fetal cardiomyocyte proliferation
|
J:99203
|
Gata4tm1.2Wtp/Gata4+
(B6.Cg-Gata4tm1.2Wtp)
|
increased apoptosis
|
J:117367
|
Gata4tm1Eno/Gata4+ Gata6tm1Eno/Gata6+
(involves: 129/Sv * 129S7/SvEvBrd * C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:111824
|
Gata4tm1Grg/Gata4+
(involves: 129 * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:185124
|
Gata4tm1Grg/Gata4tm1Grg
(involves: 129 * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:185124
|
Gata4tm1Jml/Gata4+ Gata5tm1Eem/Gata5tm1Eem
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:155855
|
Gata4tm1Wtp/Gata4tm1Wtp
(involves: 129 * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:94637
|
Gata6tm1Gsv/Gata6tm1Gsv
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB))
|
decreased inner cell mass proliferation
|
J:52029
|
Gata6tm1Msp/Gata6tm1Msp
(involves: 129X1/SvJ * C57BL/6 * CD-1)
|
increased embryonic epiblast cell apoptosis
|
J:51304
|
increased embryonic tissue cell apoptosis
|
J:51304
|
Gata6osem3Zfa/Gata6osem3Zfa Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6)
|
abnormal enterocyte proliferation
|
J:268724
|
Gatad2btm1a(EUCOMM)Hmgu/Gatad2b+
(C57BL/6N-Gatad2btm1a(EUCOMM)Hmgu)
|
abnormal epigenetic regulation of gene expression
|
J:344365
|
increased radial glial cell number
|
J:344365
|
Gatad2btm1a(EUCOMM)Hmgu/Gatad2btm1a(EUCOMM)Hmgu
(C57BL/6N-Gatad2btm1a(EUCOMM)Hmgu)
|
increased radial glial cell number
|
J:344365
|
Gatmem1Btlr/Gatmem1Btlr
(C57BL/6J-Gatmem1Btlr)
|
abnormal enterocyte proliferation
|
J:252049
|
increased enterocyte apoptosis
|
J:252049
|
Gatmm1Btlr/Gatmm1Btlr
(C57BL/6J-Gatmm1Btlr)
|
increased enterocyte apoptosis
|
J:252049
|
Gatmtm1.1Isb/Gatmtm1.1Isb
(B6.129-Gatmtm1.1Isb)
|
increased adipocyte glucose uptake
|
J:191142
|
increased muscle cell glucose uptake
|
J:191142
|
Gba1tm1.1Pmis/Gba1tm1.1Pmis Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal osteoblast differentiation
|
J:167081
|
Gba1tm1.1Pmis/Gba1tm1.2Pmis Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal osteoblast differentiation
|
J:167081
|
Gba1tm1Rlp/Gba1tm1Rlp
(involves: 129S4/SvJae * C57BL/6)
|
increased hepatocyte apoptosis
|
J:76409
|
Gba2tm1Rus/Gba2tm1Rus
(involves: 129S6/SvEv * C57BL/6J)
|
abnormal male germ cell morphology
|
J:114991
|
globozoospermia
|
J:114991
|
increased apoptosis
|
J:114991
|
oligozoospermia
|
J:114991
|
Gbe1m1Yty/Gbe1m1Yty
(C3HeB/FeJ-Gbe1m1Yty)
|
abnormal fetal cardiomyocyte proliferation
|
J:167233
|
Gbf1em1Xzha/Gbf1+
(C57BL/6J-Gbf1em1Xzha)
|
abnormal autophagosome formation
|
J:359112
|
enhanced autophagy
|
J:359112
|
increased endoplasmic reticulum stress
|
J:359112
|
Gbx2tm1.1Mrt/Gbx2tm1.1Mrt
(B6.129-Gbx2tm1.1Mrt)
|
abnormal neural crest cell migration
|
J:100584
|
abnormal vascular endothelial cell differentiation
|
J:100584
|
Gbx2tm1.1Mrt/Gbx2tm1.1Mrt Fgf8tm1.4Mrt/Fgf8+
(B6.129-Gbx2tm1.1Mrt Fgf8tm1.4Mrt)
|
abnormal neural crest cell migration
|
J:100584
|
Gctm1Nec/Gctm1Nec
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal osteoblast physiology
|
J:52225
|
Gcgrem2Smoc/Gcgrem2Smoc
(C57BL/6J-Gcgrem2Smoc)
|
increased pancreatic alpha cell proliferation
|
J:300368
|
Gcgrtm1Jcp/Gcgrtm1Jcp
(DBA/1LacJ-Gcgrtm1Jcp)
|
abnormal pancreatic alpha cell differentiation
|
J:176507
|
increased pancreatic beta cell proliferation
|
J:176507
|
Gcgrtm1Mjch/Gcgrtm1Mjch
(involves: 129 * C57BL/6J * SJL)
|
increased pancreatic alpha cell proliferation
|
J:208604
|
Gcgrtm2.1Mjch/Gcgrtm2.1Mjch Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA * SJL)
|
increased pancreatic alpha cell proliferation
|
J:208604
|
Gcktm1Hrt/Gck+ Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA)
|
abnormal mitochondrial crista morphology
|
J:250069
|
increased mitochondrial number
|
J:250069
|
Gcktm1Ydor/Gck+ Tg(Ins2-cre)25Mgn/0
(involves: C57BL/6 * C57BL/6J * DBA)
|
increased pancreatic beta cell proliferation
|
J:302600
|
Gclctm1c(EUCOMM)Wtsi/Gclc+ Tg(Cryaa-cre)10Mlr/0
(involves: 129S4/SvJaeSor * C57BL/6N * FVB/N)
|
oxidative stress
|
J:194778
|
Gclctm1c(EUCOMM)Wtsi/Gclctm1c(EUCOMM)Wtsi Tg(Cryaa-cre)10Mlr/0
(involves: 129S4/SvJaeSor * C57BL/6N * FVB/N)
|
oxidative stress
|
J:194778
|
Gclctm1Mwl/Gclctm1Mwl
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased cell proliferation
|
J:62177
|
increased embryonic tissue cell apoptosis
|
J:62177
|
Gclctm1Tdal/Gclctm1Tdal Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * DBA)
|
abnormal endoplasmic reticulum morphology
|
J:202376
|
abnormal mitochondrial morphology
|
J:202376
|
abnormal mitochondrial physiology
|
J:202376
|
decreased mitochondrial number
|
J:202376
|
Gclmtm1Tdal/Gclmtm1Tdal
(involves: 129 * C57BL/6J)
|
increased cellular sensitivity to hydrogen peroxide
|
J:80927
|
Gclmtm1Tdal/Gclmtm1Tdal
(B6.129-Gclmtm1Tdal)
|
oxidative stress
|
J:197430
|
Gclmtm1Tjka/Gclmtm1Tjka
(B6.129-Gclmtm1Tjka)
|
increased granulosa cell apoptosis
|
J:226942
|
increased granulosa cell proliferation
|
J:226942
|
oxidative stress
|
J:226942
|
Gclmtm1Tjka/Gclmtm1Tjka
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased susceptibility to neuronal excitotoxicity
|
J:129361
|
oxidative stress
|
J:129361
|
Gclmtm1Tjka/Gclmtm1Tjka
(involves: 129S1/Sv * 129X1/SvJ)
|
increased susceptibility to neuronal excitotoxicity
|
J:129045
|
oxidative stress
|
J:129045
|
Gcm1tm1Hoso/Gcm1tm1Hoso
(either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * CD-1))
|
abnormal neuron differentiation
|
J:175891
|
Gcm1tm1Hoso/Gcm1tm1Hoso Gcm2tm1Hoso/Gcm2tm1Hoso
(either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * CD-1))
|
abnormal DNA methylation
|
J:175891
|
abnormal neuron differentiation
|
J:175891
|
Gcm1tm1Jcc/Gcm1+
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
increased cell proliferation
|
J:186528
|
Gcm2tm1Hoso/Gcm2tm1Hoso
(either: (involves: 129X1/SvJ * C57BL/6) or (involves: 129X1/SvJ * CD-1))
|
abnormal DNA methylation
|
J:175891
|
abnormal neuron differentiation
|
J:175891
|
Gcn1em2Itohk/Gcn1em2Itohk
(C57BL/6-Gcn1em2Itohk)
|
abnormal cell cycle checkpoint function
|
J:287528
|
abnormal cell morphology
|
J:287528
|
abnormal fibroblast physiology
|
J:287528
|
decreased fibroblast proliferation
|
J:287528
|
increased mitotic index
|
J:287528
|
Gcnt1tm1Jxm/Gcnt1tm1Jxm
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:113195
|
impaired leukocyte tethering or rolling
|
J:113195
|
Gdap1tm1.1Ics/Gdap1tm1.1Ics
(Not Specified)
|
increased mitochondrial DNA content
|
J:221297
|
increased mitochondrial size
|
J:221297
|
oxidative stress
|
J:221297
|
Gdap1tm1.2Geno/Gdap1tm1.2Geno
(involves: 129 * C57BL/6)
|
abnormal axon extension
|
J:224701
|
abnormal endoplasmic reticulum morphology
|
J:224701
|
increased mitochondrial size
|
J:224701
|
Gdap1tm1Ics/Gdap1tm1Ics Tg(Mpz-cre)26Mes/0
(involves: FVB/NTac)
|
cellular phenotype
|
J:221297
|
Gdf1tm1Sjl/Gdf1+ Gdf3Gt(AD0857)Wtsi/Gdf3Gt(AD0857)Wtsi
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal anterior visceral endoderm cell migration
|
J:127541
|
Gdf3Gt(AD0857)Wtsi/Gdf3Gt(AD0857)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal anterior visceral endoderm cell migration
|
J:127541
|
Gdf3tm1Mms/Gdf3tm1Mms
(either: B6.129-Gdf3tm1Mms or (involves: 129S7/SvEvBrd * C57BL/6J))
|
abnormal anterior visceral endoderm cell migration
|
J:104371
|
Gdf9tm1Zuk/Gdf9tm1Zuk
(either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6))
|
abnormal oogenesis
|
J:35782
|
Gdf11tm1Clf/Gdf11tm1Clf
(involves: 129X1/SvJ * CD-1)
|
abnormal neuron differentiation
|
J:81451
|
Gdf11tm1Sjl/Gdf11tm1Sjl
(involves: 129S1/Sv * 129X1/SvJ)
|
increased apoptosis
|
J:83365
|
Gdf11tm1Sjl/Gdf11tm1Sjl
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal pancreatic beta cell differentiation
|
J:94455
|
Gdi2Gt(S1-11F1)Sor/Gdi2Gt(S1-11F1)Sor
(B6.129S4-Gdi2Gt(S1-11F1)Sor)
|
increased embryonic tissue cell apoptosis
|
J:326029
|
Gdnftm1Lmgd/Gdnf+
(B6.129-Gdnftm1Lmgd)
|
increased kidney cell proliferation
|
J:168650
|
increased mesangial cell number
|
J:168650
|
Gdpd2tm1.1Soc/Y
(involves: 129/Sv * BALB/cJ * C57BL/6J)
|
abnormal cell cycle
|
J:291492
|
increased neuronal precursor proliferation
|
J:291492
|
Gdpd2tm1.1Soc/Gdpd2+ Hprt1tm1(CMV-GFP)Nat/Hprt1+
(involves: 129/Sv * 129P2 /SvPas * 129S * BALB/cJ * C57BL/6J)
|
increased oligodendrocyte progenitor number
|
J:291492
|
Gdpd2tm1.1Soc/Gdpd2tm1.1Soc
(involves: 129/Sv * BALB/cJ * C57BL/6J)
|
abnormal cell cycle
|
J:291492
|
increased neuronal precursor proliferation
|
J:291492
|
Gdpd5tm1.1Itl/Gdpd5tm1.1Itl
(involves: 129 * C57BL/6J)
|
abnormal neuron differentiation
|
J:178550
|
abnormal neuronal precursor proliferation
|
J:178550
|
Gdpd5tm1Itl/Gdpd5tm1.1Itl Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuron differentiation
|
J:178550
|
Gen1Tn(pb-Act-RFP)1.1Zhu/Gen1Tn(pb-Act-RFP)1.1Zhu
(FVB/NJ-Gen1Tn(pb-Act-RFP)1.1Zhu)
|
cellular phenotype
|
J:330453
|
Gen1Tn(pb-Act-RFP)1.1Zhu/Gen1Tn(pb-Act-RFP)1.1Zhu
(involves: C57BL/6J * FVB/NJ)
|
cellular phenotype
|
J:330453
|
Gfaptm1Pkny/Gfaptm1Pkny
(involves: 129P2/OlaHsd * C57BL/6J)
|
cellular phenotype
|
J:125659
|
Gfaptm1Pkny/Gfaptm1Pkny Vimtm1Cba/Vimtm1Cba
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal neuron differentiation
|
J:106195
|
Gfaptm1Pkny/Gfaptm1Pkny Vimtm1Cba/Vimtm1Cba
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6)
|
decreased neuron apoptosis
|
J:123278
|
Gfaptm2Mes/Gfap+ Tg(GFAP-CRYAB)141.6Mes/0
(involves: 129S7/SvEvBrd * FVB/N)
|
abnormal cell physiology
|
J:146191
|
Gfertm1(KOMP)Mbp/Gfer+
(involves: C57BL/6J * C57BL/6N)
|
abnormal hepatocyte mitochondrial morphology
|
J:224792
|
abnormal lipid oxidation
|
J:224792
|
abnormal mitochondrial crista morphology
|
J:224792
|
abnormal mitochondrial physiology
|
J:224792
|
decreased hepatocyte mitochondrial DNA content
|
J:224792
|
decreased hepatocyte proliferation
|
J:224792
|
decreased mitochondrial number
|
J:224792
|
dilated mitochondrion
|
J:224792
|
oxidative stress
|
J:224792
|
Gfertm1.1Crg/Gfertm1.1Crg
(involves: 129 * C57BL/6)
|
abnormal mitochondrial chromosome morphology
|
J:227242
|
oxidative stress
|
J:227242
|
Gfertm1.1Crg/Gfertm1.1Crg Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129 * C57BL/6 * DBA)
|
abnormal cellular respiration
|
J:227242
|
abnormal endoplasmic reticulum morphology
|
J:227242
|
abnormal hepatocyte mitochondrial morphology
|
J:227242
|
abnormal mitochondrial crista morphology
|
J:227242
|
abnormal mitochondrial shape
|
J:227242
|
decreased mitochondrial number
|
J:227242
|
dilated mitochondrion
|
J:227242
|
increased hepatocyte apoptosis
|
J:227242
|
increased hepatocyte proliferation
|
J:227242
|
Gfi1Gen/Gfi1+
(C57BL/6J-Gfi1Gen)
|
decreased NK cell degranulation
|
J:182679
|
Gfi1tm1(cre)Gan/Gfi1+ Rfx1tm1.1Wrth/Rfx1tm1.1Wrth Rfx3tm2Wrth/Rfx3tm2Wrth
(involves: 129 * 129S7/SvEvBrd)
|
abnormal inner hair cell kinocilium morphology
|
J:227631
|
increased apoptosis
|
J:227631
|
Gfi1tm1Tmo/Gfi1tm1Tmo
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal granulocyte differentiation
|
J:75143
|
abnormal monocyte differentiation
|
J:75143
|
Gfi1tm1Wep/Gfi1tm1Wep
(B6.129-Gfi1tm1Wep)
|
abnormal T cell proliferation
|
J:117105
|
Gfi1tm1Wep/Gfi1tm1Wep Tg(Cd4-cre)1Cwi/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal T cell proliferation
|
J:117105
|
Gfi1tm5.1(GFI1*)Tmo/Gfi1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal mitosis
|
J:192927
|
Gfi1tm5.1(GFI1*)Tmo/Gfi1tm5.1(GFI1*)Tmo
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal mitosis
|
J:192927
|
Gfi1btm1.1Haho/Gfi1btm1.1Haho Tg(Mx1-cre)1Cgn/0
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:207446
|
Gfi1btm1Sho/Gfi1btm1Sho
(involves: 129S1/Sv)
|
abnormal megakaryocyte differentiation
|
J:74523
|
Gfra1tm1Jmi/Gfra1tm2Jmi Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129/Sv * C57BL/6 * CBA * SJL)
|
abnormal cell death
|
J:122607
|
abnormal cell nucleus morphology
|
J:122607
|
abnormal neuronal precursor proliferation
|
J:122607
|
Gfra3tm1Adav/Gfra3tm1Adav
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
|
abnormal neuronal precursor proliferation
|
J:71959
|
Gfra3tm1Hmd/Gfra3tm1Hmd
(involves: 129P2/OlaHsd * C57BL/6Cr)
|
abnormal neuronal migration
|
J:57342
|
increased neuron apoptosis
|
J:57342
|
Gfytm1Yyos/Gfytm1Yyos
(B6.129S-Gfytm1Yyos)
|
abnormal olfactory epithelium cilium morphology
|
J:199864
|
Ggctem1.2Smoc/Ggctem1.2Smoc
(involves: C57BL/6J)
|
decreased fibroblast proliferation
|
J:317466
|
early cellular replicative senescence
|
J:317466
|
oxidative stress
|
J:322242
|
Ggctem1.2Smoc/Ggctem1.2Smoc Krastm4Tyj/Kras+
(involves: 129S4/SvJae * C57BL/6J)
|
decreased fibroblast proliferation
|
J:317466
|
Ggcxtm1Sinos/Ggcxtm1Sinos Tg(AMH-cre)#Sinos/0
(involves: 129S2/SvPas * C57BL/6)
|
abnormal sperm flagellum morphology
|
J:307381
|
abnormal sperm head morphology
|
J:307381
|
abnormal sperm midpiece morphology
|
J:307381
|
abnormal sperm motility
|
J:307381
|
abnormal spermatid morphology
|
J:307381
|
coiled sperm flagellum
|
J:307381
|
decreased hyperactivated sperm motility
|
J:307381
|
increased male germ cell apoptosis
|
J:307381
|
increased testis apoptosis
|
J:307381
|
oligozoospermia
|
J:307381
|
teratozoospermia
|
J:307381
|
Ggntm1Dpj/Ggn+
(B6.129-Ggntm1Dpj)
|
abnormal double-strand DNA break repair
|
J:199404
|
Ggnbp1em1Lchao/Ggnbp1em1Lchao
(Not Specified)
|
abnormal acrosome morphology
|
J:297928
|
abnormal sperm head morphology
|
J:297928
|
asthenozoospermia
|
J:297928
|
kinked sperm flagellum
|
J:297928
|
teratozoospermia
|
J:297928
|
Ggnbp2Gt(IST12476F10)Tigm/Ggnbp2Gt(IST12476F10)Tigm
(involves: 129 * C57BL/6N)
|
abnormal acrosome assembly
|
J:249037
|
abnormal acrosome morphology
|
J:249037
|
abnormal manchette assembly
|
J:249037
|
abnormal spermatid morphology
|
J:249037
|
azoospermia
|
J:249037
|
decreased male germ cell number
|
J:249037
|
decreased spermatid number
|
J:249037
|
detached acrosome
|
J:249037
|
ectopic manchette
|
J:249037
|
Ggnbp2tm1Bbs/Ggnbp2tm1Bbs
(involves: 129S6/SvEvTac * C57BL/6)
|
azoospermia
|
J:270533
|
increased testis apoptosis
|
J:270533
|
Ggt1tm1Zuk/Ggt1tm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
immotile sperm
|
J:65574
|
oligozoospermia
|
J:65574
|
oocyte degeneration
|
J:65574
|
Ghitmem1Ltk/Ghitmem1Ltk
(C57BL6J-Ghitmem1Ltk)
|
abnormal hepatocyte mitochondrial morphology
|
J:327550
|
abnormal mitochondrial morphology
|
J:327550
|
Ghrtm1.1Dlr/Ghrtm1.1Dlr Tg(Ins2-cre)23Herr/0
(involves: 129S4/SvJae * C57BL/6J * CBA/J)
|
decreased pancreatic beta cell proliferation
|
J:284574
|
Ghrtm1.1Dlr/Ghrtm1.1Dlr Tg(Ins2-cre)25Mgn/0
(involves: 129S4/SvJae * C3H * C57BL/6 * DBA)
|
decreased pancreatic beta cell proliferation
|
J:173909
|
Ghrtm1Jjk/Ghrtm1Jjk
(involves: 129P2/OlaHsd * BALB/c)
|
decreased elongated spermatid number
|
J:105921
|
Gigyf2Gt(XH076)Byg/Gigyf2+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle
|
J:153971
|
Gimap5m1Btlr/Gimap5m1Btlr
(involves: C57BL/6J)
|
abnormal B cell proliferation
|
J:160090
|
abnormal colon goblet cell morphology
|
J:160090
|
decreased B cell proliferation
|
J:160090
|
Gimap6tm1.1Gwb/Gimap6tm1.1Gwb Tg(CD2-icre)4Kio/0
(involves: C57BL/6 * C57BL/10 * CBA/Ca)
|
abnormal autophagy
|
J:262059
|
abnormal mitochondrial morphology
|
J:262059
|
abnormal mitophagy
|
J:262059
|
increased T cell apoptosis
|
J:262059
|
Gins1tm1Ntak/Gins1tm1Ntak
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal inner cell mass apoptosis
|
J:119867
|
absent inner cell mass proliferation
|
J:119867
|
Gins3em1Pcamp/Gins3em1Pcamp
(C57BL/6N-Gins3em1Pcamp)
|
decreased DNA replication
|
J:331868
|
early cellular replicative senescence
|
J:331868
|
Gins4tm1Ntak/Gins4tm1Ntak
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased inner cell mass proliferation
|
J:209708
|
increased inner cell mass apoptosis
|
J:209708
|
Gipc1Gt(OST93079)Lex/Gipc1Gt(OST93079)Lex
(B6.129S-Gipc1Gt(OST93079)Lex)
|
decreased cell proliferation
|
J:122652
|
increased cell proliferation
|
J:122652
|
Git1tm1Bcb/Git1tm1Bcb
(involves: 129 * C57BL/6)
|
decreased vascular endothelial cell proliferation
|
J:158935
|
Git2Gt(XG510)Byg/Git2Gt(XG510)Byg Tg(TcraH-Y,TcrbH-Y)71Vbo/0
(involves: 129 * C57BL/6J * DBA/2J)
|
abnormal cell migration
|
J:160613
|
Git2tm1Hsb/Git2tm1Hsb
(involves: C57BL/6 * CBA)
|
abnormal neutrophil differentiation
|
J:112663
|
impaired neutrophil chemotaxis
|
J:112663
|
Gja1M1Jrt/Gja1+
(involves: C3H/HeJ * C57BL/6J)
|
decreased granulosa cell proliferation
|
J:146211
|
increased granulosa cell apoptosis
|
J:146211
|
Gja1tm1Dlg/Gja1tm1Dlg Tg(GFAP-cre)1Kdmc/0
(involves: 129S7/SvEvBrd * C3H * C57BL/6 * C57BL/6J)
|
abnormal radial glial cell morphology
|
J:156098
|
Gja1tm1Kdr/Gja1tm1Kdr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
|
decreased germ cell number
|
J:54458
|
Gja1tm1Kdr/Gja1tm1Kdr
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
decreased male germ cell number
|
J:71071
|
Gja1tm1Kdr/Gja1tm1Kdr
(involves: 129S1/Sv * 129X1/SvJ * C57BL)
|
abnormal osteoblast differentiation
|
J:65866
|
abnormal osteoblast physiology
|
J:65866
|
Gja1tm1Kwi/Gja1tm1Kwi Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
azoospermia
|
J:122838
|
decreased male germ cell number
|
J:122838
|
decreased spermatid number
|
J:122838
|
decreased spermatogonia number
|
J:122838
|
Gja1tm2(Gjb1)Kwi/Gja1+
(involves: 129P2/OlaHsd * C57BL/6)
|
maternal effect
|
J:65112
|
Gja1tm2(Gjb1)Kwi/Gja1tm2(Gjb1)Kwi
(involves: 129P2/OlaHsd * C57BL/6)
|
oligozoospermia
|
J:65112
|
Gja1tm3(Gja5)Kwi/Gja1tm3(Gja5)Kwi
(involves: 129P2/OlaHsd * C57BL/6)
|
oligozoospermia
|
J:65112
|
Gja1tm3.1Clo/Gja1tm3.1Clo
(B6.Cg-Gja1tm1.1Clo)
|
abnormal vascular smooth muscle cell proliferation
|
J:212895
|
Gja1tm7(Gja2)Kwi/Gja1tm7(Gja2)Kwi
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal spermatocyte morphology
|
J:126511
|
azoospermia
|
J:126511
|
Gja1tm8Kwi/Gja1+ Tg(Pgk1-cre)1Lni/0
(involves: 129S2/SvPas * BALB/c * C57BL/6)
|
abnormal cell physiology
|
J:132032
|
Gja4tm1Paul/Gja4tm1Paul
(either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6))
|
abnormal female meiosis
|
J:38247
|
Gjb1tm1Kwi/Y Gjc2tm1(EGFP)Kwi/Gjc2tm1(EGFP)Kwi
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
abnormal oligodendrocyte apoptosis
|
J:219594
|
Gjb2tm1Kkam/Gjb2tm1Kkam Tg(Mpz-cre)94Imeg/0
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal plasma membrane morphology
|
J:209627
|
Gjb2tm2.2Kwi/Gjb2+ Tg(Pgk1-cre)1Lni/0
(involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6)
|
increased keratinocyte proliferation
|
J:166732
|
Gjc1tm1.1Kni/Gjc1tm1.1Kni
(involves: 129S/SvEv * C57BL/6)
|
increased apoptosis
|
J:63214
|
Gjc1tm1Kni/Gjc1tm1Kni
(involves: 129S/SvEv * C57BL/6)
|
increased apoptosis
|
J:63214
|
Gjc1tm2.1Kni/Gjc1tm2.1Kni
(Not Specified)
|
increased embryonic neuroepithelium apoptosis
|
J:103078
|
Gjc1tm2Kni/Gjc1tm2Kni Tg(ACTC1-cre)1Miwa/0
(involves: C57BL/6 * DBA)
|
increased embryonic neuroepithelium apoptosis
|
J:103078
|
Gjc2tm1(EGFP)Kwi/Gjc2tm1(EGFP)Kwi Gjb1tm1Kwi/Gjb1tm1Kwi
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
abnormal oligodendrocyte apoptosis
|
J:219594
|
Gk2em1Osb/Gk2em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm mitochondrial sheath morphology
|
J:278674
|
asthenozoospermia
|
J:278674
|
kinked sperm flagellum
|
J:278674
|
Gk2em#Juhu/Gk2+
(C57BL/6J-Gk2em#Juhu)
|
abnormal sperm motility
|
J:278636
|
decreased sperm mitochondrial sheath size
|
J:278636
|
kinked sperm flagellum
|
J:278636
|
Gk2em#Juhu/Gk2em#Juhu
(C57BL/6J-Gk2em#Juhu)
|
abnormal sperm midpiece morphology
|
J:278636
|
abnormal sperm mitochondrial sheath morphology
|
J:278636
|
abnormal sperm motility
|
J:278636
|
decreased sperm mitochondrial sheath size
|
J:278636
|
kinked sperm flagellum
|
J:278636
|
oligozoospermia
|
J:278636
|
Gkap1em1Feis/Gkap1em1Feis
(involves: C57BL/6)
|
abnormal spermatocyte morphology
|
J:293924
|
Gkn2tm1.1(KOMP)Vlcg/Gkn2tm1.1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal cell differentiation
|
J:234656
|
Glatm1Kul/Y
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell morphology
|
J:39394
|
Glb1tm1Jmat/Glb1tm1Jmat
(involves: C57BL/6 * CBA * ICR)
|
abnormal macrophage chemotaxis
|
J:102576
|
Glg1Gt(RST092)Byg/Glg1+
(B6J.129P2-Glg1Gt(RST092)Byg)
|
abnormal cellular extravasation
|
J:226586
|
abnormal leukocyte adhesion
|
J:226586
|
enhanced leukocyte tethering or rolling
|
J:226586
|
Gli1tm1Alj/Gli1tm1Alj Tg(Shh)#Dje/0
(involves: 129S1/Sv * 129X1/SvJ * Swiss Webster)
|
abnormal cell proliferation
|
J:94461
|
Gli1tm2Alj/Gli1+ Gli2tm1Alj/Gli2tm1Alj Gli3Xt/Gli3Xt
(involves: 101/H * 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C3H/HeH * C57BL * CBA/H * Swiss Webster)
|
abnormal neuron differentiation
|
J:87948
|
abnormal neuronal precursor proliferation
|
J:87948
|
Gli2tm1Alj/Gli2tm1Alj
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
decreased mesenchymal cell proliferation involved in lung development
|
J:49603
|
Gli2tm1Alj/Gli2tm1Alj
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:112802
|
Gli2tm1Alj/Gli2tm1Alj Pax6Sey/Pax6Sey
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:112802
|
Gli2tm1Blnw/Gli2tm1Blnw Shhtm1Chg/Shhtm1Chg
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
cellular phenotype
|
J:145182
|
Gli3Pdn/Gli3Pdn
(involves: Jcl:ICR)
|
abnormal neuronal migration
|
J:43330
|
abnormal radial glial cell morphology
|
J:43330
|
Glipr1tm1Tt/Glipr1tm1Tt
(Not Specified)
|
decreased cellular sensitivity to alkylating agents
|
J:131419
|
Glipr2em1Blev/Glipr2em1Blev Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: C57BL/6J * DBA/2)
|
enhanced autophagy
|
J:312370
|
Glis2tm1Amj/Glis2tm1Amj
(involves: 129P2/OlaHsd * C57BL/6)
|
increased renal tubule apoptosis
|
J:134208
|
Glis2tm1Tre/Glis2tm1Tre
(B6.129P2-Glis2tm1Tre)
|
increased renal tubule apoptosis
|
J:123510
|
Glis3tm1Amj/Glis3tm1Amj
(involves: 129 * C57BL/6)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:148994
|
GlmnGt(OST109778)Lex/GlmnGt(OST109778)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
increased apoptosis
|
J:184206
|
GlmpGt(P084H04)Wrst/GlmpGt(P084H04)Wrst
(involves: 129S2/SvPas * C57BL/6)
|
abnormal lysosome morphology
|
J:208774
|
increased hepatocyte apoptosis
|
J:208774
|
oxidative stress
|
J:208774
|
Glra2tm1.2Lngu/Y Tg(mI56i-cre,EGFP)1Kc/0
(involves: 129S4/SvJae * C57BL/6J * FVB/N * MF1)
|
abnormal neuronal migration
|
J:202763
|
Glra2tm1.2Lngu/Glra2tm1.2Lngu Tg(mI56i-cre,EGFP)1Kc/0
(involves: 129S4/SvJae * C57BL/6J * FVB/N * MF1)
|
abnormal neuronal migration
|
J:202763
|
Glrx3Gt(RRF094)Byg/Glrx3Gt(RRF094)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle
|
J:190794
|
abnormal cell death
|
J:190794
|
binucleate
|
J:190794
|
decreased fibroblast proliferation
|
J:190794
|
Glrxtm1Ysh/Glrxtm1Ysh
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased sensitivity to induced cell death
|
J:125192
|
increased cellular sensitivity to oxidative stress
|
J:125192
|
Glrxtm3Ysh/Glrxtm3Ysh
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell migration
|
J:141903
|
abnormal cell physiology
|
J:141903
|
abnormal plasma membrane morphology
|
J:141903
|
decreased cell proliferation
|
J:141903
|
Glstm1a(KOMP)Mbp/Glstm1a(KOMP)Mbp
(involves: C57BL/6N)
|
cellular phenotype
|
J:241505
|
Glultm1.1Geno/Glultm1.1Geno Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * C57BL/6J * DBA)
|
oxidative stress
|
J:221031
|
Gm614tm1.1Cya/Gm614tm1.1Cya Ighg1tm1(cre)Cgn/Ighg1+
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N)
|
increased B cell apoptosis
|
J:307345
|
Gmcl1Gt(OST6847)Lex/Gmcl1Gt(OST6847)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal acrosome morphology
|
J:81819
|
abnormal cell nucleus morphology
|
J:81819
|
abnormal sperm flagellum morphology
|
J:81819
|
abnormal sperm head morphology
|
J:81819
|
abnormal sperm nucleus morphology
|
J:81819
|
abnormal spermatocyte morphology
|
J:81819
|
absent sperm flagellum
|
J:81819
|
asthenozoospermia
|
J:81819
|
globozoospermia
|
J:81819
|
multi-headed sperm
|
J:81819
|
multiflagellated sperm
|
J:81819
|
multinucleated giant male germ cells
|
J:81819
|
oligozoospermia
|
J:81819
|
teratozoospermia
|
J:81819
|
Gmcl1tm1Nkn/Gmcl1tm1Nkn
(involves: 129S2/SvPas * C57BL/6)
|
abnormal acrosome morphology
|
J:81819
|
abnormal cell nucleus morphology
|
J:81819
|
abnormal sperm flagellum morphology
|
J:81819
|
abnormal sperm head morphology
|
J:81819
|
abnormal sperm nucleus morphology
|
J:81819
|
abnormal spermatocyte morphology
|
J:81819
|
absent sperm flagellum
|
J:81819
|
asthenozoospermia
|
J:81819
|
globozoospermia
|
J:81819
|
multi-headed sperm
|
J:81819
|
multiflagellated sperm
|
J:81819
|
multinucleated giant male germ cells
|
J:81819
|
oligozoospermia
|
J:81819
|
teratozoospermia
|
J:81819
|
Gmfgtm1Jyw/Gmfgtm1Jyw
(B6.Cg-Gmfgtm1Jyw)
|
decreased lymphocyte chemotaxis
|
J:345500
|
impaired B cell migration
|
J:345500
|
Gmnctm1.1Strc/Gmnctm1.1Strc
(involves: C57BL/6 * CBA)
|
abnormal motile cilium morphology
|
J:231675
|
absent brain ependyma motile cilia
|
J:231675
|
absent oviduct epithelium motile cilium
|
J:231675
|
absent respiratory motile cilia
|
J:231675
|
azoospermia
|
J:231675
|
decreased elongated spermatid number
|
J:231675
|
increased cell death
|
J:231675
|
Gmnctm1a(KOMP)Wtsi/Gmnctm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
absent respiratory motile cilia
|
J:230806
|
GmnnGt(XT0615)Wtsi/GmnnGt(XT0615)Wtsi
(involves: 129P2/OlaHsd)
|
abnormal cell differentiation
|
J:110696
|
abnormal cell nucleus morphology
|
J:110696
|
abnormal mitosis
|
J:110696
|
Gmnntm1.1Kio/Gmnntm1.2Kio Tg(CD2-icre)4Kio/0
(involves: 129S4/SvJae * C57BL/10 * CBA/Ca)
|
decreased T cell proliferation
|
J:159657
|
Gmnntm1Nyma/Gmnntm1Nyma
(involves: C57BL/6)
|
abnormal cell adhesion
|
J:123394
|
abnormal cell nucleus morphology
|
J:123394
|
decreased cell proliferation
|
J:123394
|
Gmnntm1Tjm/Gmnntm1Tjm Tg(Mx1-cre)1Cgn/0
(involves: 129/Sv * C57BL/6 * C57BL/6J * CBA)
|
decreased hematopoietic stem cell proliferation
|
J:171741
|
Gmppatm1d(EUCOMM)Wtsi/Gmppatm1d(EUCOMM)Wtsi
(involves: C57BL/6N)
|
increased skeletal muscle cell apoptosis
|
J:305791
|
Gna12tm1.1Cgh/Gna12tm1.1Cgh Gna13tm2Cgh/Gna13tm2Cgh Tg(Mx1-cre)1Cgn/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
decreased B cell apoptosis
|
J:174313
|
Gna12tm1Citb/Gna12tm1Citb Gna13tm2.1Soff/Gna13tm2.1Soff Tg(Lck-cre)548Jxm/0
(involves: 129S1/Sv * C57BL/6 * CBA)
|
increased T cell proliferation
|
J:149560
|
Gnai2tm1Lbi/Gnai2tm1Lbi
(involves: 129S7/SvEvBrd)
|
increased T cell proliferation
|
J:30507
|
Gnai2tm1Lbi/Gnai2tm1Lbi
(B6.129S7-Gnai2tm1Lbi)
|
abnormal cellular extravasation
|
J:120069
|
abnormal leukocyte adhesion
|
J:120069
|
Gnas/Nespastm1.1Jop/Gnas+
(involves: 129S/SvEv * 129S1/Sv)
|
abnormal DNA methylation
|
J:171195
|
Gnas/Nespastm1.1Jop/Gnas+
(involves: 129S1/Sv * M. spretus)
|
abnormal DNA methylation
|
J:171195
|
Gnas/Nespastm2.1Jop/Gnas+
(involves: 129S/SvEv * 129S1/Sv)
|
abnormal DNA methylation
|
J:171195
|
GnasOedsml/Gnas+
(involves: 101/H * C3H/HeH)
|
abnormal imprinting
|
J:65007
|
Gnastm1Kel/Gnas+
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal imprinting
|
J:91703
|
Gnastm1Lsw/Gnas+
(involves: 129S4/SvJae * CD-1)
|
genetic imprinting
|
J:49340
|
increased muscle cell glucose uptake
|
J:106729
|
Gnastm2.1Lsw/Gnas+
(involves: 129S6/SvEvTac * Black Swiss)
|
maternal imprinting
|
J:97229
|
Gnastm2.1Lsw/Gnastm2.1Lsw
(involves: 129S6/SvEvTac * CD-1 * FVB/N)
|
cellular phenotype
|
J:89923
|
Gnastm2Kel/Gnas+
(either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J))
|
paternal imprinting
|
J:97634
|
Gnastm3Kel/Gnas+
(involves: 129P2/OlaHsd * C57BL/6J * DS/2)
|
abnormal imprinting
|
J:143477
|
paternal imprinting
|
J:143477
|
Gnastm4Lsw/Gnas+
(involves: 129S6/SvEvTac * Black Swiss * CD-1)
|
paternal imprinting
|
J:99237
|
Gnastm5.1Lsw/Gnastm5.1Lsw Tg(Fabp4-cre)1Abel/0
(involves: FVB)
|
increased fatty acid oxidation
|
J:159612
|
Gnasas1tm1.1Hju/Gnasas1+
(either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J))
|
abnormal DNA methylation
|
J:160293
|
abnormal imprinting
|
J:160293
|
maternal imprinting
|
J:160293
|
Gnasas1tm1.1Jop/Gnasas1+
(involves: 129S/SvEv * 129S1/Sv)
|
abnormal DNA methylation
|
J:171195
|
Gnasas1tm1.1Jop/Gnasas1+
(involves: 129S1/Sv * M. spretus)
|
abnormal DNA methylation
|
J:171195
|
Gnasas1tm1Jop/Gnasas1+
(involves: 129S/SvEv)
|
maternal imprinting
|
J:106793
|
Gnasas1tm1Jop/Gnasas1tm1.1Jop
(involves: 129S/SvEv * 129S1/Sv)
|
abnormal DNA methylation
|
J:171195
|
Gnasas1tm2.1Jop/Gnasas1+
(involves: 129S/SvEv * 129S1/Sv)
|
abnormal DNA methylation
|
J:171195
|
Gnb1Gt(prvSStrap)4B8Yiw/Gnb1Gt(prvSStrap)4B8Yiw
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal neuron differentiation
|
J:157907
|
abnormal neuronal precursor proliferation
|
J:157907
|
decreased cell proliferation
|
J:157907
|
Gng5tm1.1Rbs/Gng5tm1.1Rbs
(B6J.Cg-Gng5tm1.1Rbs)
|
decreased fetal cardiomyocyte proliferation
|
J:215128
|
increased embryonic tissue cell apoptosis
|
J:215128
|
Gnl3Gt(S4-4B1)Sor/Gnl3Gt(S4-4B1)Sor
(involves: 129S4/SvJaeSor * C57BL/6)
|
decreased cell proliferation
|
J:185271
|
increased apoptosis
|
J:185271
|
Gnl3Gt(W223E05)Wrst/Gnl3+
(Not Specified)
|
decreased cell proliferation
|
J:118144
|
Gnl3Gt(W223E05)Wrst/Gnl3Gt(W223E05)Wrst
(Not Specified)
|
abnormal cell cycle
|
J:118144
|
decreased cell proliferation
|
J:118144
|
Gnl3Gt(W223E05)Wrst/Gnl3Gt(W223E05)Wrst Trp53tm1Tyj/Trp53tm5Tyj
(involves: 129S2/SvPas * 129S4/SvJae)
|
decreased cell proliferation
|
J:118144
|
Gnl3tm1Rylt/Gnl3+
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell cycle
|
J:117592
|
decreased fibroblast proliferation
|
J:117592
|
early cellular replicative senescence
|
J:117592
|
increased fibroblast apoptosis
|
J:117592
|
Gnl3tm2.1Rylt/Gnl3tm2.1Rylt Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129 * 129S2/SvPas * C57BL/6 * CBA)
|
abnormal cell physiology
|
J:198698
|
decreased fibroblast proliferation
|
J:198698
|
Gnl3tm2.1Rylt/Gnl3tm2.1Rylt Trp53tm1Tyj/Trp53tm1Tyj Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129 * 129S2/SvPas * C57BL/6 * CBA)
|
abnormal cell death
|
J:198698
|
abnormal cell physiology
|
J:198698
|
decreased fibroblast proliferation
|
J:198698
|
Gnpattm1Just/Gnpattm1Just
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cerebellar granule cell migration
|
J:148119
|
arrest of male meiosis
|
J:84690
|
azoospermia
|
J:84690
|
Gnpnat1tm1Mak/Gnpnat1tm1Mak
(either: (involves: C57BL/6J) or (involves: CD-1))
|
decreased cell proliferation
|
J:111395
|
Gnptabnym/Gnptabnym
(involves: BALB/cAnNHsd * C3H/HeNHsd)
|
lysosomal protein accumulation
|
J:218156
|
Gnptabtm1Dkji/Gnptabtm1Dkji
(involves: 129 * C57BL/6)
|
abnormal cell morphology
|
J:231531
|
abnormal lysosome morphology
|
J:231531
|
increased lysosomal enzyme secretion
|
J:231531
|
Gnptabtm1Kkol/Gnptabtm1Kkol
(involves: 129 * C57BL/6)
|
abnormal lysosome physiology
|
J:202751
|
impaired osteoblast differentiation
|
J:202751
|
Gnrh1hpg/Gnrh1hpg
(involves: 101/H * C3H/HeH)
|
arrest of male meiosis
|
J:5877
|
GnrhrGt(181A6)Cmhd/GnrhrGt(181A6)Cmhd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal spermatocyte morphology
|
J:158384
|
Gnrhrhh/Gnrhrhh
(involves: 129S6/SvEvTac * C57BL/6)
|
arrest of male meiosis
|
J:96941
|
Gnrhrtm1Bhr/Gnrhrtm1Bhr
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:206307
|
absent sperm head
|
J:206307
|
oligozoospermia
|
J:206307
|
teratozoospermia
|
J:206307
|
Gnrhrtm2.1(GNRHR)Djb/Gnrhrtm2.1(GNRHR)Djb
(involves: 129 * C57BL/6J * FVB/N)
|
decreased male germ cell number
|
J:324870
|
Gnstm1e(EUCOMM)Hmgu/Gnstm1e(EUCOMM)Hmgu
(C57BL/6N-Atm1Brd Gnstm1e(EUCOMM)Hmgu)
|
abnormal lysosome physiology
|
J:242250
|
Golga2tm1.1Baos/Golga2tm1.1Baos Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
abnormal Golgi apparatus morphology
|
J:272184
|
abnormal Golgi cisterna morphology
|
J:272184
|
abnormal Golgi vesicle transport
|
J:272184
|
increased neuron apoptosis
|
J:272184
|
Golga2tm1.1Baos/Golga2tm1.2Baos Tg(Stra8-icre)1Reb/0
(involves: 129 * C57BL/6 * FVB/NJ)
|
abnormal sperm head morphology
|
J:273740
|
abnormal sperm mitochondrial sheath morphology
|
J:273740
|
abnormal sperm nucleus morphology
|
J:273740
|
absent acrosome
|
J:273740
|
absent sperm mitochondrial sheath
|
J:273740
|
globozoospermia
|
J:273740
|
Golga2tm1.2Baos/Golga2tm1.2Baos
(B6.129(Cg)-Golga2tm1.2Baos)
|
abnormal Golgi apparatus morphology
|
J:272184
|
abnormal Golgi vesicle transport
|
J:272184
|
Golga2tm1.2Baos/Golga2tm1.2Baos
(involves: 129 * C57BL/6)
|
abnormal acrosome assembly
|
J:273740
|
abnormal actin cytoskeleton morphology
|
J:273740
|
abnormal cell cytoskeleton morphology
|
J:273740
|
abnormal Golgi apparatus morphology
|
J:273740
|
abnormal microtubule cytoskeleton morphology
|
J:273740
|
abnormal proacrosomal vesicle fusion
|
J:273740
|
abnormal sperm head morphology
|
J:273740
|
abnormal sperm mitochondrial sheath morphology
|
J:273740
|
abnormal sperm nucleus morphology
|
J:273740
|
abnormal spermatid morphology
|
J:273740
|
absent acrosome
|
J:273740
|
absent sperm mitochondrial sheath
|
J:273740
|
decreased sperm progressive motility
|
J:273740
|
globozoospermia
|
J:273740
|
immotile sperm
|
J:273740
|
oligozoospermia
|
J:273740
|
Golga3repro27/Golga3repro27
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal male germ cell apoptosis
|
J:199215
|
abnormal sperm head morphology
|
J:199215
|
absent sperm flagellum
|
J:92463
|
asthenozoospermia
|
J:92463,
J:199215
|
azoospermia
|
J:199215
|
decreased male germ cell number
|
J:199215
|
detached sperm flagellum
|
J:199215
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
teratozoospermia
|
J:199215
|
Golga3Tg(06MGMT)T604Kccri/Golga3Tg(06MGMT)T604Kccri
(involves: C3H * C57BL/6)
|
abnormal sperm head morphology
|
J:52847
|
oligozoospermia
|
J:52847
|
Golga5em2Lanyu/Golga5em2Lanyu
(FVB/NJ-Golga5em2Lanyu)
|
cellular phenotype
|
J:242905
|
Golga5em3Lanyu/Golga5em3Lanyu
(FVB/NJ-Golga5em3Lanyu)
|
cellular phenotype
|
J:242905
|
Golgb1m1Lanyu/Golgb1m1Lanyu
(A/J-Golgb1m1Lanyu)
|
cellular phenotype
|
J:235669
|
Gopctm1.1Tno/Gopctm1.1Tno
(involves: 129S4/SvJae)
|
abnormal sperm flagellum morphology
|
J:124177
|
coiled sperm flagellum
|
J:124177
|
globozoospermia
|
J:124177
|
Gopctm1.1Tno/Gopctm1.1Tno
(involves: 129S4/SvJae * C57BL/6)
|
abnormal acrosome morphology
|
J:78599
|
abnormal sperm mitochondrial sheath morphology
|
J:78599
|
abnormal sperm nucleus morphology
|
J:78599
|
absent acrosome
|
J:78599
|
asthenozoospermia
|
J:78599
|
coiled sperm flagellum
|
J:78599
|
detached acrosome
|
J:78599
|
globozoospermia
|
J:78599
|
Gopctm1a(EUCOMM)Wtsi/Gopctm1a(EUCOMM)Wtsi
(C57BL/6-Gopctm1a(EUCOMM)Wtsi)
|
abnormal cell physiology
|
J:232679
|
GorabGt(XG183)Byg/GorabGt(XG183)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal nonmotile primary cilium morphology
|
J:231070
|
Gorasp1tm1a(KOMP)Catr/Gorasp1tm1a(KOMP)Catr
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal Golgi cis cisterna morphology
|
J:211288
|
cellular phenotype
|
J:211288
|
Gorasp2tm1.1Maal/Gorasp2tm1.1Maal
(B6J.129S2(Cg)-Gorasp2tm1.1Maal)
|
abnormal acrosome morphology
|
J:241919
|
abnormal Golgi apparatus morphology
|
J:241919
|
abnormal sperm head morphology
|
J:241919
|
abnormal sperm midpiece morphology
|
J:241919
|
abnormal spermatocyte morphology
|
J:241919
|
asthenozoospermia
|
J:241919
|
oligozoospermia
|
J:241919
|
Gp1batm1Ware/Gp1batm1Ware
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal megakaryocyte differentiation
|
J:63389
|
Gpa33tm1Jkhh/Gpa33tm1Jkhh
(involves: 129 * C57BL/6)
|
decreased colon goblet cell number
|
J:231808
|
Gpat2tm1.1Nkn/Gpat2tm1.1Nkn
(involves: 129S2/SvPas * C57BL/6NSlc)
|
abnormal DNA methylation during gametogenesis
|
J:277128
|
abnormal male germ cell morphology
|
J:277128
|
abnormal spermatocyte morphology
|
J:277128
|
azoospermia
|
J:277128
|
increased male germ cell apoptosis
|
J:277128
|
Gpc3tm1Arge/Y H19tm1Tilg/H19+
(involves: 129S/SvEv * 129S1/Sv)
|
paternal imprinting
|
J:75054
|
Gpc3tm1Arge/Y Igf2tm1Rob/Igf2+
(involves: 129S/SvEv * 129S1/Sv * C57BL/6J)
|
maternal imprinting
|
J:75054
|
Gpc3tm1Arge/Gpc3+ Igf2tm1Rob/Igf2+
(involves: 129S/SvEv * 129S1/Sv * C57BL/6J)
|
maternal imprinting
|
J:75054
|
Gpc3tm1Arge/Gpc3tm1Arge H19tm1Tilg/H19+
(involves: 129S/SvEv * 129S1/Sv)
|
paternal imprinting
|
J:75054
|
Gpc3tm1Snd/Y
(involves: 129X1/SvJ * C57BL/6)
|
abnormal osteoclast differentiation
|
J:104555
|
patent ductus arteriosus
|
J:154375
|
Gpc6tm1Lex/Gpc6tm1Lex
(B6N.129S5(B6)-Gpc6tm1Lex/Mmucd)
|
decreased chondrocyte proliferation
|
J:245694
|
Gpcpd1tm1c(EUCOMM)Hmgu/Gpcpd1tm1c(EUCOMM)Hmgu Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6J * C57BL/6N * FVB)
|
increased cardiac muscle cell glucose uptake
|
J:345630
|
increased muscle cell glucose uptake
|
J:345630
|
gpg1/gpg1
(involves: BALB/cAnN * C3H/HeH)
|
abnormal motile primary cilium morphology
|
J:145068
|
gpg3/gpg3
(involves: BALB/cAnN * C3H/HeH)
|
abnormal motile primary cilium morphology
|
J:145068
|
Gphntm1Jrs/Gphntm1Jrs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal axon extension
|
J:98106
|
Gpm6atm1.1Tahi/Gpm6atm1.1Tahi
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal axon extension
|
J:184737
|
Gpm6btm1KanPlp1tm1Kan/Y
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal oligodendrocyte apoptosis
|
J:193310
|
increased apoptosis
|
J:193310
|
Gpr3tm1Cled/Gpr3tm1Cled
(either: B6.129-Gpr3tm1Cled or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
abnormal female meiosis
|
J:105182
|
abnormal oocyte morphology
|
J:105182
|
abnormal oogenesis
|
J:105182
|
maternal effect
|
J:105182
|
Gpr4tm1Witt/Gpr4tm1Witt
(either: B6.129X1-Gpr4tm1Witt or (involves: 129X1/SvJ * C57BL/6))
|
decreased mesangial cell number
|
J:118276
|
Gpr34tm1.1Shbg/Gpr34tm1.1Shbg
(B6.Cg-Gpr34tm1.1Shbg)
|
abnormal leukocyte migration
|
J:168120
|
Gpr37tm1.1Ryot/Gpr37tm1.1Ryot
(involves: C57BL/6)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:128745
|
Gpr37l1tm1.2Gtva/Gpr37l1tm1.2Gtva
(involves: 129S/SvEv * BALB/c * C57BL/6J)
|
abnormal Bergmann glial cell differentiation
|
J:201190
|
abnormal neuronal precursor proliferation
|
J:201190
|
abnormal Purkinje cell differentiation
|
J:201190
|
Gpr37l1tm1.2Gtva/Gpr37l1tm1.2Gtva Ptch1tm1Zim/Ptch1+
(STOCK Gpr37l1tm1.2Gtva Ptch1tm1Zim/Cnrm)
|
decreased cerebellar granule cell precursor proliferation
|
J:272049
|
Gpr55tm1.1Mijr/Gpr55tm1.1Mijr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal osteoclast differentiation
|
J:153225
|
Gpr68tm1.1Yaxu/Gpr68tm1.1Yaxu
(B6.Cg-Gpr68tm1.1Yaxu)
|
abnormal osteoclast differentiation
|
J:149315
|
Gpr68tm1.1Yaxu/Gpr68tm1.1Yaxu
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal osteoclast differentiation
|
J:149315
|
Gpr68tm1Yaxu/Gpr68tm1Yaxu
(involves: C57BL/6)
|
abnormal osteoclast differentiation
|
J:149315
|
Gpr75tm1(KOMP)Vlcg/Gpr75tm1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
increased retina apoptosis
|
J:341992
|
oxidative stress
|
J:341992
|
Gpr107tm1Brs/Gpr107tm1Brs
(involves: 129S6/SvEvTac)
|
abnormal vesicle-mediated transport
|
J:215242
|
Gpr132tm1Witt/Gpr132tm1Witt
(B6.129X1-Gpr132tm1Witt)
|
impaired macrophage chemotaxis
|
J:96613
|
Gpr132tm1Witt/Gpr132tm1Witt
(involves: 129X1/SvJ * BALB/c)
|
increased B cell proliferation
|
J:69473
|
increased T cell proliferation
|
J:69473
|
Gpr132tm1Witt/Gpr132tm1Witt Ldlrtm1Her/Ldlrtm1Her
(B6.129-Ldlrtm1Her Gpr132tm1Witt)
|
decreased macrophage apoptosis
|
J:100498
|
Gpr161tm1.2Smuk/Gpr161tm1.2Smuk H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: C57BL/6J * CBA/J)
|
increased neuronal precursor proliferation
|
J:316181
|
Gpr174tm1Cys/Y
(B6.129-Gpr174tm1Cys)
|
increased T cell proliferation
|
J:222307
|
Gpr183tm1.2Rbr/Gpr183tm1.2Rbr Ightm1Rbr/Ightm1Rbr Tg(IgkHyHEL10)1Rbr/0
(involves: C57BL/6 * FVB/N * SJL)
|
abnormal B cell proliferation
|
J:151883
|
impaired B cell migration
|
J:151883
|
Gprc6atm1.1Kry/Gprc6atm1.1Kry Tg(Cyp17a1-icre)AJako/0
(involves: C57BL/6J)
|
increased male germ cell apoptosis
|
J:170888
|
oligozoospermia
|
J:170888
|
Gpsm2tm1.2Fuma/Gpsm2tm1.2Fuma
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal cell differentiation
|
J:132370
|
Gpsm2tm1a(EUCOMM)Wtsi/Gpsm2tm1a(EUCOMM)Wtsi
(C57BL/6-Gpsm2tm1a(EUCOMM)Wtsi)
|
abnormal cell cytoskeleton morphology
|
J:214064
|
abnormal kinocilium morphology
|
J:214064
|
Gpsm3Gt(IST12408A1)Tigm/Gpsm3Gt(IST12408A1)Tigm
(involves: C57BL/6N)
|
abnormal leukocyte migration
|
J:193270
|
Gpt2tm1a(KOMP)Wtsi/Gpt2tm1a(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal tricarboxylic acid cycle
|
J:238353
|
Gpx1tm1Kola/Gpx1tm1Kola
(involves: 129S2/SvPas * BALB/c * CF-1)
|
increased neuron apoptosis
|
J:71798,
J:79183
|
oxidative stress
|
J:71798
|
Gpx1tm1Kola/Gpx1tm1Kola
(involves: 129S2/SvPas * CF-1)
|
abnormal cell cycle
|
J:87985
|
abnormal cell morphology
|
J:87985
|
cellular necrosis
|
J:87985
|
decreased cell proliferation
|
J:87985
|
increased cellular sensitivity to hydrogen peroxide
|
J:87985
|
increased cellular sensitivity to oxidative stress
|
J:87985,
J:49644
|
Gpx1tm1Mgr/Gpx1tm1Mgr
(involves: 129 * C57BL/6J)
|
abnormal mitochondrial physiology
|
J:62395
|
Gpx1tm1Ysh/Gpx1tm1Ysh
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
decreased cellular sensitivity to gamma-irradiation
|
J:63988
|
Gpx1tm1Ysh/Gpx1tm1Ysh
(B6.129-Gpx1tm1Ysh)
|
decreased cellular sensitivity to gamma-irradiation
|
J:63988
|
Gpx4tm1.1Qra/Gpx4tm1.1Qra Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal cellular respiration
|
J:183246
|
increased hepatocyte apoptosis
|
J:183246
|
Gpx4tm1Ssd/Gpx4+
(B6.129-Gpx4tm1Ssd)
|
abnormal mitochondrial physiology
|
J:134214
|
oxidative stress
|
J:134214
|
Gpx4tm1Yana/Gpx4tm1Yana
(involves: C57BL/6 * CBA)
|
abnormal apoptosis
|
J:83472
|
Gpx4tm1Yana/Gpx4tm1Yana Tg(Crx-cre)1Tfur/0 Tg(Gpx4)#Yana/0
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2)
|
abnormal photoreceptor connecting cilium morphology
|
J:182776
|
decreased mitochondrial DNA content
|
J:182776
|
Gpx4tm1Yana/Gpx4tm1Yana Tg(Gpx4)#Yana/0 Tg(Pgk2-cre)24Shb/0
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * DBA/2 * ICR)
|
abnormal male germ cell morphology
|
J:156326
|
abnormal mitochondrial crista morphology
|
J:156326
|
abnormal mitochondrial physiology
|
J:156326
|
abnormal sperm mitochondrial morphology
|
J:156326
|
asthenozoospermia
|
J:156326
|
decreased male germ cell number
|
J:156326
|
hairpin sperm flagellum
|
J:156326
|
oligozoospermia
|
J:156326
|
Gpx4tm2Marc/Gpx4tm2Marc Tg(Camk2a-cre)2Gsc/0
(involves: 129P2/OlaHsd * FVB/N)
|
increased neuron apoptosis
|
J:139668
|
Gpx4tm3Marc/Gpx4tm3Marc
(involves: 129P2/OlaHsd)
|
abnormal sperm head morphology
|
J:186906
|
abnormal sperm mitochondrial sheath morphology
|
J:186906
|
abnormal sperm principal piece morphology
|
J:186906
|
cellular phenotype
|
J:186906
|
increased sperm mitochondrial size
|
J:186906
|
kinked sperm flagellum
|
J:186906
|
Gpx4tm4Marc/Gpx4+
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal sperm head morphology
|
J:225651
|
abnormal sperm midpiece morphology
|
J:225651
|
abnormal sperm motility
|
J:225651
|
increased sperm mitochondrial size
|
J:225651
|
kinked sperm flagellum
|
J:225651
|
Gpx5tm1115.2Arte/Gpx5tm1115.2Arte
(involves: C57BL/6 * C57BL/6N)
|
abnormal sperm nucleus morphology
|
J:152563
|
Gpx7tm1Whle/Gpx7tm1Whle
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cellular sensitivity to hydrogen peroxide
|
J:193993
|
increased cellular sensitivity to oxidative stress
|
J:193993
|
increased fibroblast apoptosis
|
J:193993
|
oxidative stress
|
J:193993
|
Graptm1Gsf/Graptm1Gsf
(B6.129-Graptm1Gsf)
|
increased T cell proliferation
|
J:76243
|
Grb2tm1Lnit/Grb2tm1Lnit Cd79atm1(cre)Reth/Cd79a+
(involves: BALB/c * BALB/cJ)
|
increased B cell apoptosis
|
J:171222
|
increased B cell proliferation
|
J:171222
|
Grb2tm1Paw/Grb2tm1Paw
(involves: 129S1/Sv * 129X1/SvJ)
|
absent inner cell mass proliferation
|
J:51424
|
Grb7tm1d(EUCOMM)Wtsi/Grb7tm1d(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
maternal effect
|
J:344139
|
Grb10Gt(Betageo)1Ward/Grb10+
(involves: C57BL/6 * CBA)
|
paternal imprinting
|
J:84425
|
Grb10tm1.1Fliu/Grb10tm1.1Fliu Tg(Adipoq-cre)#Pesch/0
(involves: 129S/SvEv * FVB)
|
decreased fatty acid oxidation
|
J:213603
|
Grb10tm1.1Fliu/Grb10tm1.1Fliu Tg(Pdx1-cre)6Tuv/0
(involves: 129S/SvEv * C57BL/6 * FVB/N)
|
increased pancreatic beta cell proliferation
|
J:208498
|
Grem1tm1Azun/Grem1tm1Azun
(either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
increased apoptosis
|
J:90991
|
increased metanephric mesenchyme apoptosis
|
J:90991
|
Grem1tm1Ecan/Grem1tm1Rmh Tg(BGLAP-cre)1Clem/0
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N)
|
enhanced osteoblast differentiation
|
J:126375
|
Grhl3tm1Bogi/Grhl3tm1Bogi
(involves: C57BL/6J)
|
abnormal keratinocyte differentiation
|
J:114626
|
increased keratinocyte proliferation
|
J:114626
|
Grhl3tm1Jane/Grhl3tm1Jane
(involves: 129S1/Sv)
|
increased keratinocyte proliferation
|
J:178952
|
Gria2tm1Rod/Gria2+
(B6.129-Gria2tm1Rod/J)
|
increased susceptibility to neuronal excitotoxicity
|
J:104951
|
Gria2tm1Rod/Gria2tm1Rod
(B6.129-Gria2tm1Rod/J)
|
increased susceptibility to neuronal excitotoxicity
|
J:104951
|
Gria2tm1Rsp/Gria2+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:30145
|
Gria2tm2Rsp/Gria2+ Tg(Camk2a-cre)1Gsc/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
abnormal neuron differentiation
|
J:111689
|
Gria2tm3Rsp/Gria2tm3Rsp Tg(Camk2a-cre)1Gsc/0
(involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * FVB/N)
|
abnormal neuron differentiation
|
J:111689
|
Grid2ho-4J/Grid2ho-4J
(DBA/2J-Grid2ho-4J/J)
|
abnormal Purkinje cell mitochondrial morphology
|
J:137190
|
Grid2ho-Jwg/Grid2ho-Jwg
(Not Specified)
|
abnormal sperm flagellum morphology
|
J:10295
|
abnormal sperm motility
|
J:10295
|
Grid2Lc/Grid2ho-Nancy
(involves: C57BL/6 * STOCK MitfMi-wh)
|
abnormal autophagy
|
J:82240
|
Grin1tm1Nak/Grin1tm1Nak
(involves: 129S/Sv * C57BL/6 * DBA/2)
|
decreased susceptibility to neuronal excitotoxicity
|
J:38582
|
Grk1tm1Citb/Grk1tm1Citb
(involves: 129X1/SvJ * C57BL/6)
|
abnormal retina apoptosis
|
J:54021
|
Grk2tm1Gwd/Grk2tm1Mca Tg(Cd4-cre)1Cwi/0
(involves: 129 * C57BL/6 * DBA/2)
|
impaired leukocyte tethering or rolling
|
J:176118
|
Grk6tm1.1Mca/Grk6tm1.1Mca
(B6.129S4-Grk6tm1.1Mca)
|
impaired macrophage phagocytosis
|
J:225063
|
Grm1Tg(p18A4.B)1352Szc/0
(Not Specified)
|
abnormal melanocyte proliferation
|
J:32786
|
Grm2tm1Nak/Grm2tm1Nak
(B6.129S-Grm2tm1Nak)
|
decreased susceptibility to neuronal excitotoxicity
|
J:202321
|
Grntm1.1Far/Grntm1.1Far
(involves: 129S4/SvJae * C57BL/6J * FVB/N)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:188324
|
Grntm1.1Geno/Grntm1.1Geno
(involves: 129 * C57BL/6J)
|
increased hepatocyte karyomegaly
|
J:188420
|
Grntm1.1Hiok/Grn+
(involves: C57BL/6J)
|
abnormal cell cycle checkpoint function
|
J:308471
|
abnormal endoplasmic reticulum morphology
|
J:308471
|
cellular necrosis
|
J:308471
|
Grntm1Far/Grntm1Far Tg(ITGAM-cre)2781Gkl/0
(involves: 129S4/SvJae * C57BL/6 * CBA * FVB/N)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:188324
|
gro25/gro25
(Not Specified)
|
azoospermia
|
J:85113
|
gro26/gro26
(Not Specified)
|
azoospermia
|
J:85113
|
Grxcr1pi/Grxcr1pi
(B6.C3-Grxcr1pi/J)
|
absent inner hair cell kinocilia
|
J:94385
|
Grxcr2tm1.1Dck/Grxcr2tm1.1Dck
(B6.Cg-Grxcr2tm1.1Dck)
|
abnormal outer hair cell kinocilium morphology
|
J:265041
|
Gsdmdem1Fcw/Gsdmdem2Fcw
(involves: C57BL/6)
|
abnormal macrophage apoptosis
|
J:226781
|
Gsdmdem3Fcw/Gsdmdem3Fcw
(involves: C57BL/6)
|
abnormal macrophage apoptosis
|
J:226781
|
Gsdmdem4Fcw/Gsdmdem4Fcw
(C57BL/6N-Gsdmdem4Fcw/J)
|
abnormal macrophage apoptosis
|
J:101977
|
Gsk3atm1.2Svij/Gsk3a+
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal sperm head morphology
|
J:221688
|
abnormal sperm midpiece morphology
|
J:221688
|
Gsk3atm1.2Svij/Gsk3atm1.2Svij
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal sperm head morphology
|
J:221688
|
abnormal sperm midpiece morphology
|
J:221688
|
asthenozoospermia
|
J:221688
|
oligozoospermia
|
J:221688
|
Gsk3btm1Jrw/Gsk3b+
(involves: 129 * C57BL/6)
|
abnormal osteoblast physiology
|
J:129364
|
enhanced osteoblast differentiation
|
J:129364
|
Gsk3btm1Jrw/Gsk3b+ Irs2tm1Mfw/Irs2tm1Mfw
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal pancreatic islet cell apoptosis
|
J:135659
|
increased pancreatic beta cell proliferation
|
J:135659
|
Gsntm1Djk/Gsntm1Djk
(either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6))
|
abnormal osteoclast differentiation
|
J:60625
|
impaired neutrophil chemotaxis
|
J:24346
|
Gsta4tm1Pzim/Gsta4tm1Pzim
(involves: 129S1/Sv * 129S6/SvEvTac)
|
oxidative stress
|
J:87983
|
Gstk1tm1Pgb/Gstk1tm1Pgb
(BALB/c-Gstk1tm1Pgb)
|
cellular phenotype
|
J:177201
|
Gstm1tm1Gcw/Gstm1tm1Gcw
(involves: 129S/SvEv * C57BL/6)
|
increased neuron apoptosis
|
J:159701
|
Gstz1tm1Jmfc/Gstz1tm1Jmfc
(129S4/SvJae-Gstz1tm1Jmfc)
|
increased kidney apoptosis
|
J:77040
|
oxidative stress
|
J:77040
|
Gstz1tm1Pgb/Gstz1tm1Pgb
(BALB/c-Gstz1tm1Pgb/AnuApb)
|
abnormal hepatocyte mitochondrial morphology
|
J:91519
|
cellular necrosis
|
J:91519
|
Gsx2tm2.2Kc/Gsx2tm2.2Kc
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL)
|
abnormal neuron differentiation
|
J:154936
|
Gt(ROSA)26Sor/Gt(ROSA)26Sor Igs4tm1Hsas/Igs4tm1Hsas
(involves: 129S4/SvJae * 129S7/SvEvBrd)
|
abnormal cell physiology
|
J:192826
|
Gt(ROSA)26Sor/Gt(ROSA)26Sor Igs4tm1Hsas/Igs4tm1Hsas Tg(CAG-cre)13Miya/0
(involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6)
|
cellular phenotype
|
J:192826
|
Gt(ROSA)26Sorem1(CAG-Zfas1)Cya/Gt(ROSA)26Sor+ Tg(Myh6-cre)#Cya/0
(involves: C57BL/6J)
|
increased cardiomyocyte apoptosis
|
J:294533
|
Gt(ROSA)26Sorem1(Tbc1d15)Jren/Gt(ROSA)26Sorem1(Tbc1d15)Jren A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: C57BL/6N * FVB/N)
|
abnormal mitochondrial physiology
|
J:341775
|
Gt(ROSA)26Sortm1(Bcor*A)Vjba/Gt(ROSA)26Sortm1(Bcor*A)Vjba
(involves: 129S1/Sv)
|
decreased cell proliferation
|
J:231455
|
Gt(ROSA)26Sortm1(Bmi1)Aiwa/Gt(ROSA)26Sor+ Tg(Tek-cre)1Ywa/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
increased hematopoietic stem cell proliferation
|
J:198331
|
Gt(ROSA)26Sortm1(CAG-Bcl3,-EGFP)Hoev/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd)
|
decreased B cell apoptosis
|
J:208980
|
decreased B cell proliferation
|
J:208980
|
Gt(ROSA)26Sortm1(CAG-Bgeo,-Insc/GFP)Jakn/Gt(ROSA)26Sortm1(CAG-Bgeo,-Insc/GFP)Jakn Tg(Nes-cre)1Wmz/0
(involves: C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:178712
|
abnormal radial glial cell morphology
|
J:178712
|
Gt(ROSA)26Sortm1(CAG-cas9*,-EGFP)Fezh/? Tmem258tm1.1(KOMP)Vlcg/Tmem258+
(involves: C57BL/6NTac)
|
increased cell death
|
J:240635
|
increased endoplasmic reticulum stress
|
J:240635
|
Gt(ROSA)26Sortm1(CAG-LMNA*)Cyh/Gt(ROSA)26Sor+ Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6JNarl * FVB)
|
abnormal cell nucleus morphology
|
J:284048
|
abnormal endoplasmic reticulum morphology
|
J:284048
|
abnormal mitochondrial crista morphology
|
J:284048
|
increased endoplasmic reticulum stress
|
J:284048
|
Gt(ROSA)26Sortm1(CAG-MFN2*T105M)Dple/Gt(ROSA)26Sor+ Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * CBA)
|
abnormal mitochondrial morphology
|
J:251584
|
Gt(ROSA)26Sortm1(CAG-MFN2*T105M)Dple/Gt(ROSA)26Sor+ Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
decreased mitochondrial number
|
J:251584
|
Gt(ROSA)26Sortm1(CAG-NPM1*)Geno/Gt(ROSA)26Sor+ Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal megakaryocyte differentiation
|
J:196690
|
Gt(ROSA)26Sortm1(CAG-NPM1*)Geno/Gt(ROSA)26Sortm1(CAG-NPM1*)Geno Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal megakaryocyte differentiation
|
J:196690
|
Gt(ROSA)26Sortm1(CAG-Nr2f2)Tsa/Gt(ROSA)26Sor+ A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal cell physiology
|
J:227012
|
abnormal mitochondrial inner membrane morphology
|
J:227012
|
abnormal mitochondrial physiology
|
J:227012
|
abnormal mitochondrial shape
|
J:227012
|
abnormal oxidative phosphorylation
|
J:227012
|
abnormal respiratory electron transport chain
|
J:227012
|
decreased fatty acid oxidation
|
J:227012
|
Gt(ROSA)26Sortm1(CAG-Slc39a14*L438R)Wvh/Gt(ROSA)26Sor+ Tg(Runx2-icre)1Jtuc/0
(involves: FVB/N)
|
abnormal osteoblast physiology
|
J:261326
|
Gt(ROSA)26Sortm1(CAG-Wnt5a,-AcGFP)Skde/Gt(ROSA)26Sor+ Pgrtm2(cre)Lyd/Pgr+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal trophoblast giant cell proliferation
|
J:233595
|
Gt(ROSA)26Sortm1(CARD14*)Ribt/Gt(ROSA)26Sor+ Tg(KRT14-cre/ERT)20Efu/0
(involves: 129S6/SvEvTac * C57BL/6NCrl * CD-1)
|
increased keratinocyte proliferation
|
J:292094
|
Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+ Id1tm3Bene/Id1tm3Bene Id2tm1Xdz/Id2tm1Xdz Id3tm1Zhu/Id3tm1Zhu
(involves: 129S4/SvJaeSor * C57BL/6)
|
premature neuronal precursor differentiation
|
J:185426
|
Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+ Kat8tm1Thl/Kat8+
(involves: 129S1/Sv)
|
abnormal DNA repair
|
J:128936
|
decreased fibroblast proliferation
|
J:128936
|
increased cellular sensitivity to ionizing radiation
|
J:128936
|
Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+ Kat8tm1Thl/Kat8tm1Thl
(involves: 129S1/Sv)
|
decreased fibroblast proliferation
|
J:128936
|
Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+ Mcl1tm1Ywh/Mcl1tm1Ywh
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6)
|
increased T cell apoptosis
|
J:137400
|
Gt(ROSA)26Sortm1(cre/ERT2)Thl/Gt(ROSA)26Sor+ Pknox1tm1.1Rygo/Pknox1tm1.1Rygo
(involves: 129 * C57BL/6 * C57BL/6JJcl)
|
abnormal spermatogonia morphology
|
J:258387
|
azoospermia
|
J:258387
|
decreased male germ cell number
|
J:258387
|
increased testis apoptosis
|
J:258387
|
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/0 Smc5tm1c(KOMP)Wtsi/Smc5tm1d(KOMP)Wtsi
(involves: 129S4/SvJae * C57BL/6N * CBA)
|
abnormal cell cycle
|
J:240155
|
abnormal cell differentiation
|
J:240155
|
abnormal mitosis
|
J:240155
|
abnormal mitotic spindle assembly checkpoint
|
J:240155
|
abnormal mitotic spindle morphology
|
J:240155
|
cellular phenotype
|
J:240155
|
increased cell death
|
J:240155
|
increased mitotic index
|
J:240155
|
mitotic nondisjunction
|
J:240155
|
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+ Sprtntm1.1Yjm/Sprtntm1.1Yjm
(involves: 129S/SvEv * 129S4/SvJae)
|
chromosomal instability
|
J:297179
|
Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+ Supt5tm1.1Rrp/Supt5tm1.2Rrp
(involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6)
|
abnormal fibroblast physiology
|
J:319843
|
Gt(ROSA)26Sortm1(cre/ERT)Brn/Gt(ROSA)26Sor+ Lin9tm1.1Sgau/Lin9+
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal mitotic spindle assembly checkpoint
|
J:162678
|
Gt(ROSA)26Sortm1(cre/ERT)Brn/Gt(ROSA)26Sor+ Lin9tm1.1Sgau/Lin9tm1.1Sgau
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal cell nucleus morphology
|
J:162678
|
abnormal centrosome morphology
|
J:162678
|
abnormal mitosis
|
J:162678
|
abnormal small intestinal crypt cell proliferation
|
J:162678
|
decreased fibroblast proliferation
|
J:162678
|
Gt(ROSA)26Sortm1(cre/ERT)Brn/Gt(ROSA)26Sor+ Ppp1r13ltm1Xlu/Ppp1r13ltm1Xlu
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J)
|
abnormal cell cycle
|
J:177360
|
abnormal keratinocyte differentiation
|
J:177360
|
decreased fibroblast proliferation
|
J:177360
|
early cellular replicative senescence
|
J:177360
|
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+ Ikbkbtm1Lex/Ikbkbtm1Lex
(involves: 129S/SvEvBrd)
|
abnormal fibroblast migration
|
J:159873
|
decreased fibroblast cell migration
|
J:159873
|
decreased fibroblast chemotaxis
|
J:159873
|
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+ Tardbptm1.1Pcw/Tardbptm1.1Pcw
(involves: 129 * C57BL/6 * SJL)
|
abnormal lipid oxidation
|
J:164406
|
Gt(ROSA)26Sortm1(Crh)Jde/Gt(ROSA)26Sortm1(Crh)Jde Tg(Nes-cre)1Kln/0
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
decreased susceptibility to neuronal excitotoxicity
|
J:140968
|
Gt(ROSA)26Sortm1(DTA)Lky/Gt(ROSA)26Sortm1(DTA)Lky
(involves: 129P2/OlaHsd)
|
abnormal cell death
|
J:133382
|
Gt(ROSA)26Sortm1(DTA)Vlcg/Gt(ROSA)26Sortm1(DTA)Vlcg Tg(BGLAP-cre/ERT2)#Stko/0
(involves: 129S1/Sv * FVB/N)
|
decreased pancreatic beta cell proliferation
|
J:201507
|
increased apoptosis
|
J:201507
|
Gt(ROSA)26Sortm1(ETV6/SYK)Hjum/Gt(ROSA)26Sor+ Cd79atm3(cre/ERT2)Reth/Cd79a+
(involves: 129S6/SvEvTac * BALB/c)
|
increased B cell apoptosis
|
J:208904
|
increased B cell proliferation
|
J:208904
|
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ Hprt1tm1(Ins2-HBEGF)Herr/Y Tg(Gcg-rtTA)#Herr/0 Tg(tetO-cre)1Jaw/0
(involves: 129X1/SvJ * C57BL/6)
|
abnormal pancreatic alpha cell differentiation
|
J:159291
|
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ Plcg1tm1Gcrp/Plcg1tm1Rwen Tg(Cd4-cre)1Cwi/0
(involves: 129X1/SvJ * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:157757
|
increased T cell apoptosis
|
J:157757
|
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ Resttm1.1Jhsi/Resttm1.1Jhsi Tg(Nes-cre/ERT2)KEisc/0
(involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:174056
|
premature neuronal precursor differentiation
|
J:174056
|
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+ Rev3ltm1.1Diaz/Rev3ltm1.1Diaz
(involves: 129P2/OlaHsd * 129X1/SvJ * BALB/c * C57BL/6 * C57BL/6NTac)
|
decreased B cell proliferation
|
J:188723
|
Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sortm1(EYFP)Cos Pax7tm1(cre/ERT2)Gaka/Pax7tm1(cre/ERT2)Gaka Paxbp1tm1.1Nju/Paxbp1tm1.1Nju
(involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6NCr)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:304562
|
abnormal mitochondrial morphology
|
J:304562
|
abnormal oxidative phosphorylation
|
J:304562
|
abnormal respiratory electron transport chain
|
J:304562
|
decreased mitochondrial fission
|
J:304562
|
Gt(ROSA)26Sortm1(Gck)Ydor/Gt(ROSA)26Sor+ Tg(Pdx1-cre/Esr1*)#Dam/0
(involves: C57BL/6 * CBA)
|
decreased pancreatic beta cell proliferation
|
J:210493
|
Gt(ROSA)26Sortm1(GNAQ*)Cvrk/Gt(ROSA)26Sor+ Tg(Mitf-cre)7114Gsb/0
(C3FeJ.Cg-Gt(ROSA)26Sortm1(GNAQ*)Cvkr Tg(Mitf-cre)7114Gsb/Cvrk)
|
abnormal melanocyte proliferation
|
J:225597
|
Gt(ROSA)26Sortm1(GNAQ*)Cvrk/Gt(ROSA)26Sortm14(CAG-tdTomato)Hze Tg(Mitf-cre)7114Gsb/0
(C3FeJ.Cg-Gt(ROSA)26Sortm1(GNAQ*)Cvrk/Gt(ROSA)26Sortm14(CAG-tdTomato)Hze Tg(Mitf-cre)7114Gsb/Cvrk)
|
abnormal cell physiology
|
J:312561
|
abnormal melanocyte proliferation
|
J:312561
|
Gt(ROSA)26Sortm1(gp80,EGFP)Eces/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+
(either: (involves: 129/Sv * 129P2/OlaHsd * C57BL/6) or (involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6))
|
decreased B cell apoptosis
|
J:172031
|
Gt(ROSA)26Sortm1(Grem1)Svok/Gt(ROSA)26Sor+ Tg(Prrx1-cre)1Cjt/0
(involves: 129S1/Sv * C57BL/6J * SJL/J)
|
decreased apoptosis
|
J:214075
|
increased cell proliferation
|
J:214075
|
Gt(ROSA)26Sortm1(H1/tetO-RNAi:Fxn)Dhg/Gt(ROSA)26Sor+
(B6.129-Gt(ROSA)26Sortm1(H1/tetO-RNAi:Fxn)Dhg)
|
disorganized mitochondrial cristae
|
J:254962
|
increased mitochondrial size
|
J:254962
|
Gt(ROSA)26Sortm1(HBEGF)Awai/Gt(ROSA)26Sor+ Tg(Krt1-15-cre/PGR*)22Cot/0
(involves: C57BL/6J * SJL/J)
|
increased cell proliferation
|
J:244536
|
Gt(ROSA)26Sortm1(HBEGF)Awai/Gt(ROSA)26Sortm1(HBEGF)Awai Mogtm1(cre)Gkl/?
(involves: C57BL/6)
|
increased neuron apoptosis
|
J:131076
|
Gt(ROSA)26Sortm1(HBEGF)Awai/Gt(ROSA)26Sortm1(HBEGF)Awai Tg(Gdf9-icre)5092Coo/0
(involves: C57BL/6)
|
abnormal female germ cell apoptosis
|
J:157008
|
abnormal granulosa cell apoptosis
|
J:157008
|
Gt(ROSA)26Sortm1(Hoxa2)Fmr/Gt(ROSA)26Sor+ Olig2tm2(TVA,cre)Rth/Olig2+
(involves: 129P2/OlaHsd)
|
decreased oligodendrocyte progenitor number
|
J:193058
|
Gt(ROSA)26Sortm1(ITK/SYK)Jrld/Gt(ROSA)26Sor+ Tg(Cd4-cre)1Cwi/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
increased T cell proliferation
|
J:160931
|
Gt(ROSA)26Sortm1(Myc)Rcse/Gt(ROSA)26Sortm1(Myc)Rcse Tg(Wap-cre)11738Mam/0
(involves: 129 * C57BL/6 * SJL)
|
abnormal chromosome number
|
J:169403
|
chromosomal instability
|
J:169403
|
Gt(ROSA)26Sortm1(Notch1)Dam/Gt(ROSA)26Sor+ Tg(Adipoq-cre)1Evdr/0
(involves: 129S4/SvJaeSor * C57BL/6J * FVB/NJ)
|
abnormal white fat cell differentation
|
J:237232
|
Gt(ROSA)26Sortm1(RNU6-RNAi:Rad18)Wbaa/Gt(ROSA)26Sor+
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:177475
|
abnormal spermatid morphology
|
J:177475
|
abnormal synaptonemal complex
|
J:177475
|
oligozoospermia
|
J:177475
|
Gt(ROSA)26Sortm1(rtTA)Awu/Gt(ROSA)26Sor+ Hif1atm3Rsjo/Hif1atm3Rsjo Tg(tetO-cre)LC1Bjd/0
(involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
abnormal cell migration
|
J:130751
|
Gt(ROSA)26Sortm1(rtTA,EGFP)Nagy/Gt(ROSA)26Sor+ Tg(Col2a1-cre)1Bhr/0 Tg(tetO-Vegfa)90Ala/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL)
|
abnormal osteoblast differentiation
|
J:156474
|
Gt(ROSA)26Sortm1(Smo/EYFP)Amc/Gt(ROSA)26Sor+ Hk2tm1.1Uku/Hk2tm1.1Uku Tg(GFAP-cre)25Mes/0
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N)
|
abnormal neuronal precursor proliferation
|
J:210113
|
Gt(ROSA)26Sortm1(tetO-Sox9)Msan/Gt(ROSA)26Sor+ Tg(SFTPC-rtTA)5Jaw/0
(Not Specified)
|
abnormal cell differentiation
|
J:202984
|
Gt(ROSA)26Sortm1(Trpv1,ECFP)Mde/Gt(ROSA)26Sor+ Tg(Nes-cre)1Wme/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
increased susceptibility to neuronal excitotoxicity
|
J:136582
|
Gt(ROSA)26Sortm1(tTA,tetO-Mir155)Fjsl/Gt(ROSA)26Sor+ Tg(Nes-cre)1Wmz/0
(involves: 129 * C57BL/6 * FVB/N * SJL/J)
|
increased apoptosis
|
J:185598
|
Gt(ROSA)26Sortm1(Wnt4)Bhr/Gt(ROSA)26Sor+ Tg(Col2a1-cre)1Bhr/0
(involves: 129S7/SvEvBrd * C57BL/6 * SJL)
|
decreased chondrocyte proliferation
|
J:129327
|
Gt(ROSA)26Sortm1.1(CAG-COX8A/Dendra2)Dcc/Gt(ROSA)26Sor+ MffGt(AZ0438)Wtsi/MffGt(AZ0438)Wtsi
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:301349
|
abnormal sperm connecting piece morphology
|
J:301349
|
abnormal sperm midpiece morphology
|
J:301349
|
abnormal sperm mitochondrial sheath morphology
|
J:301349
|
abnormal sperm principal piece morphology
|
J:301349
|
abnormal spermatid morphology
|
J:301349
|
asthenozoospermia
|
J:301349
|
decreased mitochondrial number
|
J:301349
|
kinked sperm flagellum
|
J:301349
|
Gt(ROSA)26Sortm1.1(CAG-COX8A/Dendra2)Dcc/Gt(ROSA)26Sor+ Mfn2tm3Dcc/Mfn2tm3Dcc Slc6a3tm1.1(cre)Bkmn/Slc6a3+
(involves: 129 * 129S6/SvEvTac * C57BL/6J * SJL/J)
|
abnormal mitochondrial morphology
|
J:188347
|
Gt(ROSA)26Sortm1.1(CAG-Mirc20)Eem/Gt(ROSA)26Sor+ A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129 * C57BL/6 * FVB/N)
|
decreased cardiomyocyte apoptosis
|
J:233994
|
Gt(ROSA)26Sortm1.1(CAG-Mirc20)Eem/Gt(ROSA)26Sor+ Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:233994
|
increased fetal cardiomyocyte proliferation
|
J:233994
|
Gt(ROSA)26Sortm1.1(CAG-Trp53*,-EGFP)Medz/Gt(ROSA)26Sortm1.1(CAG-Trp53*,-EGFP)Medz
(involves: C57BL/6)
|
decreased thymocyte apoptosis
|
J:158953
|
Gt(ROSA)26Sortm1.1(CAG-Upp1,-GFP)Gp/Gt(ROSA)26Sor+
(involves: C57BL/6 * FVB/N)
|
decreased fatty acid beta-oxidation
|
J:195165
|
Gt(ROSA)26Sortm1.1(CAG-YFP/DROSHA*E1147K)Gess/Gt(ROSA)26Sortm1.1(CAG-YFP/DROSHA*E1147K)Gess Tg(Six2-EGFP/cre)1Amc/0
(involves: 129S6/SvEvTac * C57BL/6 * CD-1)
|
increased kidney apoptosis
|
J:321428
|
Gt(ROSA)26Sortm1.1(Loxl2)Acan/Gt(ROSA)26Sortm1.1(Loxl2)Acan
(Not Specified)
|
abnormal keratinocyte differentiation
|
J:220689
|
Gt(ROSA)26Sortm1.1(Lyn/Celsr1/EGFP)Rodr/Gt(ROSA)26Sor+
(involves: FVB/N)
|
abnormal anterior visceral endoderm cell migration
|
J:170681
|
Gt(ROSA)26Sortm1.1(Lyn/Celsr1/EGFP)Rodr/Gt(ROSA)26Sortm1.1(Lyn/Celsr1/EGFP)Rodr
(involves: FVB/N)
|
abnormal anterior visceral endoderm cell migration
|
J:170681
|
Gt(ROSA)26Sortm1.1(Maml1/EGFP)Hri/? Foxa2tm3.1(icre)Heli/Foxa2+
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal pancreatic beta cell differentiation
|
J:184814
|
Gt(ROSA)26Sortm1.1(MYC/ERT2)Gev/Gt(ROSA)26Sortm1.1(MYC/ERT2)Gev
(involves: C57BL/6 * FVB/N)
|
increased apoptosis
|
J:142030
|
increased cell proliferation
|
J:142030
|
Gt(ROSA)26Sortm1.1(Otx2)Daac/Gt(ROSA)26Sor+ Slc6a3tm1.1(cre)Bkmn/Slc6a3+
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:166896
|
Gt(ROSA)26Sortm1.1(Otx2)Daac/Gt(ROSA)26Sortm1.1(Otx2)Daac Slc6a3tm1.1(cre)Bkmn/Slc6a3+
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:166896
|
Gt(ROSA)26Sortm1.1(Otx2)Daac/Gt(ROSA)26Sortm1.1(Otx2)Daac Slc6a3tm1.1(cre)Bkmn/Slc6a3+ Tg(CAG-Otx2,-GFP)21Asim/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:166896
|
Gt(ROSA)26Sortm1.1(Sstr3/GFP)Bky/Gt(ROSA)26Sor+
(involves: C57BL/6 * C57BL/6NTac * FVB/N)
|
asthenozoospermia
|
J:199240
|
hairpin sperm flagellum
|
J:199240
|
Gt(ROSA)26Sortm1.1(Ubc-BCL3)Sbn/Gt(ROSA)26Sor+ Cd79atm1(cre)Reth/Cd79a+
(involves: BALB/c * C57BL/6)
|
decreased B cell proliferation
|
J:207111
|
Gt(ROSA)26Sortm1Lrsn/Gt(ROSA)26Sor+ Mfn2tm1.1Arte/Mfn2tm1.1Arte Slc6a3tm1(cre)Lrsn/Slc6a3+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal mitochondrial shape
|
J:188337
|
decreased mitochondrial number
|
J:188337
|
increased mitochondrial size
|
J:188337
|
Gt(ROSA)26Sortm1Lrsn/Gt(ROSA)26Sor+ Slc6a3tm1(cre)Lrsn/Slc6a3+ Tfamtm1Lrsn/Tfamtm1Lrsn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal mitochondrial physiology
|
J:176022
|
Gt(ROSA)26Sortm1Sho/0 Itga5tm2Hyn/Itga5tm1Hyn Itgavtm1Hyn/Itgavtm2Hyn Tg(Tek-cre)1Ywa/0
(involves: 129 * C57BL/6 * SJL)
|
patent ductus arteriosus
|
J:161850
|
Gt(ROSA)26Sortm1Sho/0 Itga5tm2Hyn/Itga5tm1Hyn Itgavtm2Hyn/Itgav+ Tg(Tek-cre)1Ywa/0
(involves: 129 * C57BL/6 * SJL)
|
patent ductus arteriosus
|
J:161850
|
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Krastm4Tyj/Kras+ Pms2tm2(cre)Lisk/Pms2tm2(cre)Lisk
(involves: 129S4/SvJae * 129S4/SvJaeSor)
|
abnormal mismatch repair
|
J:204653
|
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Pdss2tm1.1Jdhu/Pdss2tm1.2Jdhu Tg(Pcp2-cre)3555Jdhu/0
(involves: 129 * C3H/HeNCr MMTV- * C57BL/6N * FVB/N)
|
increased neuron apoptosis
|
J:179845
|
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Pms2tm2(cre)Lisk/Pms2tm2(cre)Lisk
(involves: 129S4/SvJaeSor)
|
abnormal mismatch repair
|
J:204653
|
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Snrpbem1Lajm/Snrpb+ Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
(involves: 129S4/SvJaeSor * C57BL/6J * CD1 * FVB/N)
|
increased cranial neural crest cell apoptosis
|
J:326544
|
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Tg(Nphs1-cre)33Mska/0 Tg(Nphs1-IL2RA)18Mska/0
(involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * DBA/2)
|
increased kidney cell proliferation
|
J:126591
|
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sortm1Sor Tg(NPHS2-rtTA2*M2)1Jbk/Tg(NPHS2-rtTA2*M2)1Jbk Tg(tetO-cre)LC1Bjd/Tg(tetO-cre)LC1Bjd
(involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB/N)
|
aneuploidy
|
J:285673
|
Gt(ROSA)26Sortm2(ATF4)Myz/Gt(ROSA)26Sortm2(ATF4)Myz Tg(Myh11-icre/ERT2)1Soff/?
(either: D2.Cg-Atf4tm1.1Cmad Tg(Myh11-icre/ERT2)1Soff or B6.Cg-Atf4tm1.1Cmad Tg(Myh11-icre/ERT2)1Soff)
|
increased cardiomyocyte apoptosis
|
J:237331
|
Gt(ROSA)26Sortm2(CAG-Dsred2/EGFP)Luo/Gt(ROSA)26Sortm1(Notch3*)Sfr Notch3tm1.1(cre/ERT2)Sat/Notch3+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac)
|
decreased mammary gland epithelial cell proliferation
|
J:201985
|
Gt(ROSA)26Sortm2(CAG-Lancl1)Pfw/Gt(ROSA)26Sor+ Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6 * FVB)
|
abnormal male germ cell apoptosis
|
J:324139
|
abnormal redox activity
|
J:324139
|
abnormal sperm progressive motility
|
J:324139
|
decreased cellular sensitivity to oxidative stress
|
J:324139
|
increased sperm motility
|
J:324139
|
Gt(ROSA)26Sortm2(CAG-Lancl1)Pfw/Gt(ROSA)26Sortm2(CAG-Lancl1)Pfw Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
decreased susceptibility to neuronal excitotoxicity
|
J:214805
|
Gt(ROSA)26Sortm2(CAG-Notch2*)Uzs/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J)
|
increased B cell proliferation
|
J:179036
|
Gt(ROSA)26Sortm2(DTA)Riet/Gt(ROSA)26Sortm2(DTA)Riet Tg(Gdf9-icre)5092Coo/0
(involves: 129P2/OlaHsd * C57BL/6)
|
absent oocytes
|
J:157008
|
Gt(ROSA)26Sortm2(Gli2*)Flng/Gt(ROSA)26Sor+ Ihhtm1Amc/Ihhtm1Amc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoblast differentiation
|
J:154905
|
Gt(ROSA)26Sortm2(Gli2*)Flng/Gt(ROSA)26Sor+ Ihhtm1Amc/Ihhtm1Amc Tg(Col2a1-cre)3Amc/0
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoblast differentiation
|
J:154905
|
Gt(ROSA)26Sortm2(H1/tetO-RNAi:Kdm1a)Arte/Gt(ROSA)26Sor+
(involves: C57BL/6)
|
abnormal granulocyte differentiation
|
J:192055
|
abnormal monocyte differentiation
|
J:192055
|
increased hematopoietic stem cell proliferation
|
J:192055
|
Gt(ROSA)26Sortm2(Lmp1/CD40)Uzs/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * BALB/c * C57BL/6)
|
increased B cell proliferation
|
J:137122
|
Gt(ROSA)26Sortm2(Mirn150)Rsky/Gt(ROSA)26Sortm2(Mirn150)Rsky
(involves: C57BL/6 * SJL/J)
|
increased B cell apoptosis
|
J:127234
|
Gt(ROSA)26Sortm2(myc*T58A)Rcse/Gt(ROSA)26Sortm2(myc*T58A)Rcse Tg(Wap-cre)11738Mam/0
(involves: 129 * C57BL/6 * SJL)
|
aneuploidy
|
J:169403
|
chromosomal instability
|
J:169403
|
polyploidy
|
J:169403
|
Gt(ROSA)26Sortm2(Pax3)Joe/Gt(ROSA)26Sortm2(Pax3)Joe Pax3tm1(cre)Joe/Pax3+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal osteoblast differentiation
|
J:137730
|
Gt(ROSA)26Sortm2(Rnf187)Jhai/Gt(ROSA)26Sor+ Krastm4Tyj/Kras+ Tg(Vil1-cre)20Syr/0
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * DBA/2)
|
abnormal enterocyte proliferation
|
J:173145
|
Gt(ROSA)26Sortm2.1(Mirn150)Rsky/Gt(ROSA)26Sortm2.1(Mirn150)Rsky
(involves: C57BL/6 * SJL/J)
|
increased B cell apoptosis
|
J:127234
|
Gt(ROSA)26Sortm2.1(MYC/ERT)Hsc/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor)
|
increased cell proliferation
|
J:89756
|
Gt(ROSA)26Sortm2Bet/Gt(ROSA)26Sortm2Bet Speer6-ps1Tg(Alb-cre)21Mgn/?
(involves: BALB/c * C57BL/6 * DBA)
|
increased hepatocyte proliferation
|
J:174261
|
Gt(ROSA)26Sortm2Sho/Gt(ROSA)26Sor+ Sp8tm1Smb/Sp8tm1Smb H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J * CBA/J)
|
decreased cranial neural crest cell proliferation
|
J:200761
|
increased cranial neural crest cell apoptosis
|
J:200761
|
increased embryonic neuroepithelium apoptosis
|
J:200761
|
increased head mesenchyme apoptosis
|
J:200761
|
Gt(ROSA)26Sortm3(CAG-EYFP)Hze/Gt(ROSA)26Sor+ Hiratm1c(EUCOMM)Wtsi/Hiratm1d(EUCOMM)Wtsi Tg(Myh6-cre)2182Mds/0
(B6.Cg-Gt(ROSA)26Sortm3(CAG-EYFP)Hze Hiratm1c(EUCOMM)Wtsi/Hiratm1d(EUCOMM)Wtsi Tg(Myh6-cre)2182Mds)
|
oxidative stress
|
J:231593
|
Gt(ROSA)26Sortm3(CAG-MIR17-92,-EGFP)Rsky/Gt(ROSA)26Sortm3(CAG-MIR17-92,-EGFP)Rsky Tg(CD2-icre)4Kio/0
(involves: C57BL/6 * C57BL/10 * CBA/Ca)
|
increased B cell proliferation
|
J:133215
|
increased mesangial cell number
|
J:133215
|
Gt(ROSA)26Sortm3(HIF1A*)Kael/Gt(ROSA)26Sortm4(HIF2A*)Kael Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * BALB/c * C57BL/6 * DBA)
|
increased hepatocyte proliferation
|
J:144666
|
Gt(ROSA)26Sortm3(Irf4)Evdr/Gt(ROSA)26Sor+ Tg(Ucp1-cre)1Evdr/0
(involves: 129 * C57BL/6J * FVB)
|
abnormal cellular respiration
|
J:214637
|
Gt(ROSA)26Sortm3(myc*S62A)Rcse/Gt(ROSA)26Sortm3(myc*S62A)Rcse Tg(Wap-cre)11738Mam/0
(involves: 129 * C57BL/6 * SJL)
|
aneuploidy
|
J:169403
|
chromosomal instability
|
J:169403
|
polyploidy
|
J:169403
|
Gt(ROSA)26Sortm3(Runx2)Flng/Gt(ROSA)26Sortm3(Runx2)Flng Ihhtm1Amc/Ihhtm1Amc Tg(Col2a1-cre)3Amc/0
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoblast differentiation
|
J:180304
|
Gt(ROSA)26Sortm3(SS18/EGFP)Mrc/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell death
|
J:147728
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/? Tg(BGLAP-cre)1Clem/? Trip11tm1.1Psmi/Trip11tm1.2Psmi
(involves: 129/Sv * C57BL/6 * FVB/NJ)
|
abnormal Golgi stack morphology
|
J:253969
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ Srsf3tm1Pjln/Srsf3tm1Pjln
(involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6J * CBA/J)
|
decreased cranial neural crest cell apoptosis
|
J:308882
|
decreased cranial neural crest cell proliferation
|
J:308882
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Pfkfb3tm1Pec/Pfkfb3tm1Pec Tg(Cdh5-cre/ERT2)1Rha/0
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased endothelial cell proliferation
|
J:200070
|
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Pfkfb3tm1Pec/Pfkfb3tm1Pec Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased endothelial cell proliferation
|
J:200070
|
Gt(ROSA)26Sortm4(H1/tetO-RNAi:Ezh2)Arte/Gt(ROSA)26Sor+
(C57BL/6-Gt(ROSA)26Sortm4(H1/tetO-RNAi:Ezh2)Arte)
|
decreased mammary gland epithelial cell proliferation
|
J:202724
|
Gt(ROSA)26Sortm4(HIF2A*)Kael/Gt(ROSA)26Sor+ Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * BALB/c * C57BL/6 * DBA)
|
increased hepatocyte proliferation
|
J:144666
|
Gt(ROSA)26Sortm4(HIF2A*)Kael/Gt(ROSA)26Sor+ Tg(KRT14-cre)1Ipc/0
(involves: 129S6/SvEvTac * BALB/c * C57BL/6 * SJL)
|
increased keratinocyte proliferation
|
J:144666
|
Gt(ROSA)26Sortm5(ACTB-tTA)Luo/Gt(ROSA)26Sor+ Tg(Col2a1-cre)1Bhr/0 Tg(tetO/CMV-Col2a1*R992C,-GFP)#Afe/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL)
|
abnormal primary cilium morphology
|
J:216945
|
Gt(ROSA)26Sortm5(H1/tetO-RNAi:Ezh2)Arte/Gt(ROSA)26Sor+
(C57BL/6-Gt(ROSA)26Sortm5(H1/tetO-RNAi:Ezh2)Arte)
|
decreased mammary gland epithelial cell proliferation
|
J:202724
|
Gt(ROSA)26Sortm6(tetO-dTomato,-Ctnnb1*)Bgh/Gt(ROSA)26Sor+
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell physiology
|
J:187862
|
Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky/Gt(ROSA)26Sor+ Tg(CAG-cre/Esr1*)5Amc/0
(B6.Cg-Gt(ROSA)26Sortm7(Pik3ca*,EGFP)Rsky Tg(CAG-cre/Esr1*)5Amc)
|
increased cell proliferation
|
J:264410
|
Gt(ROSA)26Sortm9(cre/ESR1)Arte/? Tnfaip3tm1Homy/Tnfaip3tm1Homy
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac)
|
increased apoptosis
|
J:212681
|
Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ Map3k14tm1.1Gne/Map3k14tm1.1Gne
(B6(Cg)-Map3k14tm1.1Gne Gt(ROSA)26Sortm9(cre/ESR1)Arte)
|
decreased B cell proliferation
|
J:240453
|
Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ Pkn2tm1c(KOMP)Wtsi/Pkn2tm1c(KOMP)Wtsi
(involves: C57BL/6N * C57BL/6NTac)
|
abnormal mitosis
|
J:229595
|
decreased fibroblast proliferation
|
J:229595
|
decreased mitotic index
|
J:229595
|
increased embryonic tissue cell apoptosis
|
J:229595
|
Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ Rnf2tm1Mvi/Rnf2tm1Mvi
(involves: 129S/Sv * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal neuron differentiation
|
J:154927
|
Gt(ROSA)26Sortm10(Lmp1)Rsky/Gt(ROSA)26Sor+
(involves: BALB/cJ)
|
increased B cell proliferation
|
J:181546
|
Gt(ROSA)26Sortm10(Lmp1)Rsky/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * BALB/cJ)
|
increased B cell proliferation
|
J:181546
|
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+
(involves: C57BL/6)
|
increased B cell proliferation
|
J:181546
|
Gt(ROSA)26Sortm11(Lmp1)Rsky/Gt(ROSA)26Sor+ Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:181546
|
Gt(ROSA)26Sortm12.1Sia/Gt(ROSA)26Sor+ Haus6tm1.2Sdwb/Haus6tm1.2Sdwb
(B6.Cg-Haus6tm1.2Sdwb Gt(ROSA)26Sortm12.1Sia)
|
abnormal mitotic spindle morphology
|
J:235084
|
Gt(ROSA)26Sortm16Jhai/Gt(ROSA)26Sor+ Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr * CBA)
|
cellular phenotype
|
J:195147
|
Gt(ROSA)26Sortm37(H1/tetO-RNAi:Tafazzin)Arte/?
(Not Specified)
|
abnormal mitochondrial morphology
|
J:176041
|
abnormal mitochondrial physiology
|
J:176041
|
Gt(ROSA)26Sortm37(H1/tetO-RNAi:Tafazzin)Arte/Gt(ROSA)26Sor+
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased mitochondrial fission
|
J:167527
|
increased mitochondrial number
|
J:167527
|
Gt(ROSA)26Sortm407(H1/tetO-RNAi:Large)Arte/Gt(ROSA)26Sor+
(B6.Cg-Gt(ROSA)26Sortm407(H1/tetO-RNAi:Large)Arte)
|
abnormal basement membrane morphology
|
J:206057
|
Gtf2a1tm1.1Jjdh/Gtf2a1tm1.1Jjdh
(involves: 129X1/SvJ * C57BL/6)
|
azoospermia
|
J:205038
|
decreased elongated spermatid number
|
J:205038
|
increased male germ cell apoptosis
|
J:205038
|
Gtf2itm1Vcam/Gtf2itm1Vcam
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
decreased embryonic epiblast cell proliferation
|
J:204278
|
Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1+ Tg(MtTGFA)42Lmb/0
(involves: C57BL/6 * CBA * CD-1)
|
increased hepatocyte apoptosis
|
J:34434
|
increased hepatocyte karyomegaly
|
J:34434
|
Gtpbp2nmf205/Gtpbp2nmf205 n-TRtct5m1J/n-TRtct5m1J
(C57BL/6J-Gtpbp2nmf205/J)
|
abnormal ribosomal stalling
|
J:211326
|
increased neuron apoptosis
|
J:211326
|
Gtpbp2tm1Ynim/Gtpbp2tm1Ynim n-TRtct5m1J/n-TRtct5m1J
(B6.Cg-Gtpbp2tm1Ynim)
|
increased neuron apoptosis
|
J:211326
|
Gtsf1tm1Miya/Gtsf1tm1Miya
(involves: 129P2/OlaHsd * C57BL/6)
|
arrest of male meiosis
|
J:154374
|
increased male germ cell apoptosis
|
J:154374
|
oligozoospermia
|
J:154374
|
teratozoospermia
|
J:154374
|
Guca2atm1.1Mcoh/Guca2atm1.1Mcoh
(involves: 129P2/OlaHsd * BALB/c)
|
abnormal enterocyte proliferation
|
J:80545
|
Guf1tm1.1Nju/Guf1tm1.1Nju
(involves: 129 * C57BL/6 * FVB/N)
|
abnormal sperm mitochondrial sheath morphology
|
J:333298
|
asthenozoospermia
|
J:333298
|
increased male germ cell apoptosis
|
J:333298
|
oligozoospermia
|
J:333298
|
Guf1tm1Nju/Guf1tm1Nju Alpltm1(cre)Nagy/Alpl+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
oligozoospermia
|
J:333298
|
Gulosfx/Gulosfx
(BALB/cBy-Gulosfx/J)
|
abnormal osteoclast differentiation
|
J:66648
|
Gulp1tm1.2Kimj/Gulp1tm1.2Kimj
(involves: 129S4/SvJae * C57BL/6 * SJL)
|
abnormal osteoclast differentiation
|
J:340688
|
Gusbmps-2J/Gusbmps-2J
(C3H/HeOuJ-Gusbmps-2J/BrkJ)
|
abnormal lysosome morphology
|
J:72372,
J:50358
|
Gusbmps/Gusbmps
(B6.C-H2-Kbm1/ByBir-Gusbmps/J)
|
abnormal lysosome morphology
|
J:9705
|
Gusbmps/Gusbmps
(B6.Cg-Gusbmps/BrkJ)
|
abnormal cell morphology
|
J:21256
|
abnormal lysosome morphology
|
J:21256
|
Gusbmps/Gusbmps KitW-41J/KitW-41J
(B6(C)-KitW-41J Gusbmps/BrkJ)
|
abnormal lysosome morphology
|
J:58272
|
Gusbtm1Sly/Gusbtm1Sly
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal lysosome morphology
|
J:81792
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:81792
|
Gusbtm2Sly/Gusbtm2Sly
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal lysosome morphology
|
J:81792
|
Gusbtm3Sly/Gusbtm3Sly
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal lysosome morphology
|
J:81792
|
Gy/Y
(involves: 101/H * C3H/HeH)
|
oligozoospermia
|
J:8335
|
Gyg1tm1a(KOMP)Wtsi/Gyg1tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal cellular respiration
|
J:244440
|
abnormal lipid oxidation
|
J:244440
|
Gykl1em#Juhu/Gykl1+
(C57BL/6J-Gykl1em#Juhu)
|
abnormal sperm motility
|
J:278636
|
decreased sperm mitochondrial sheath size
|
J:278636
|
kinked sperm flagellum
|
J:278636
|
Gykl1em#Juhu/Gykl1em#Juhu
(C57BL/6J-Gykl1em#Juhu)
|
abnormal sperm flagellum morphology
|
J:278636
|
abnormal sperm mitochondrial sheath morphology
|
J:278636
|
abnormal sperm motility
|
J:278636
|
decreased sperm mitochondrial sheath size
|
J:278636
|
kinked sperm flagellum
|
J:278636
|
oligozoospermia
|
J:278636
|
Gys1Gt(OST33395)Lex/Gys1Gt(OST33395)Lex
(involves: 129S5/SvEvBrd * 129X1/SvJ * C57BL/6J)
|
abnormal fetal cardiomyocyte proliferation
|
J:92245
|
Gys1tm1.1Arte/Gys1tm1.1Arte
(involves: C57BL/6J)
|
abnormal muscle cell glucose uptake
|
J:167911
|
Gys2tm1.1Pro/Gys2tm1.1Pro Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA)
|
decreased cardiac muscle cell glucose uptake
|
J:162043
|
Gzmbtm1Ley/Gzmbtm1Ley
(involves: 129X1/SvJ)
|
decreased T cell apoptosis
|
J:126114
|
Gzmbtm1Ley/Gzmbtm1Ley Serpinb9tm1.1Pib/Serpinb9tm1.1Pib
(involves: 129S2/SvPas * BALB/cJ * C57BL/6J)
|
decreased cytotoxic T cell apoptosis
|
J:252016
|
H1f1em1Ibbr/H1f1em1Ibbr
(C57BL/6J-H1f1em1Ibbr)
|
maternal effect
|
J:337428
|
H1f1tm1Drab/H1f1tm1Drab Smcptm1Wen/Smcptm1Wen Tnp2tm1Wen/Tnp2tm1Wen
(involves: 129 * C57BL/6J)
|
asthenozoospermia
|
J:98301
|
impaired sperm migration in female genital tract
|
J:98301
|
H1f2tm1Ais/H1f2tm1Ais
(involves: 129P2/OlaHsd * C57BL)
|
decreased cellular sensitivity to X-ray irradiation
|
J:107681
|
H1f6tm1Drab/H1f6tm1Drab Smcptm1Wen/Smcptm1Wen Tnp2tm1Wen/Tnp2tm1Wen
(involves: 129 * C57BL/6J)
|
asthenozoospermia
|
J:98301
|
H1f7tm1Idvd/H1f7tm1Idvd
(Not Specified)
|
abnormal sperm head morphology
|
J:96828
|
abnormal sperm nucleus morphology
|
J:96828
|
asthenozoospermia
|
J:96828
|
detached acrosome
|
J:96828
|
oligozoospermia
|
J:96828
|
H1f7tm1Yoni/H1f7tm1Yoni
(involves: 129S1/Sv * C57BL/6)
|
asthenozoospermia
|
J:119846
|
teratozoospermia
|
J:119846
|
H2-Ab1b-tm1Doi/H2-Ab1b-tm1Doi
(involves: 129S2/SvPas)
|
abnormal neuron proliferation
|
J:170591
|
H2-DMatm2Liz/H2-DMatm2Liz
(involves: C57BL/6 * C57BL/10 * C57BR * CBA)
|
decreased T cell proliferation
|
J:111565
|
H2-Oa/Brd2Tg(otx2-lacZ)F5pImat/H2-Oa/Brd2Tg(otx2-lacZ)F5pImat
(involves: CD-1)
|
abnormal cell cycle
|
J:188139
|
increased embryonic neuroepithelium apoptosis
|
J:188139
|
H2-Oa/Brd2Tg(otx2-lacZ)F5pImat/H2-Oa/Brd2Tg(otx2-lacZ)F5pImat
(involves: CD-1)
|
abnormal cell cycle
|
J:188139
|
increased embryonic neuroepithelium apoptosis
|
J:188139
|
H2b/H2b Nfkbidtm1Clay/Nfkbidtm1Clay Rag2tm1Fwa/Rag2tm1Fwa Tg(TcraN15,TcrbN15)L2Elre/?
(involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6)
|
decreased T cell proliferation
|
J:132071
|
H2b/H2b Rag2tm1Fwa/Rag2tm1Fwa Tg(TcraN15,TcrbN15)L2Elre/?
(involves: 129S/SvEv * C57BL/6)
|
increased T cell proliferation
|
J:133112
|
H2ab1em1TtasH2ab2em1TtasH2ab3em1Ttas/Y
(FVB/NJArc-H2ab2em1Ttas H2ab1em1Ttas H2ab3em1Ttas)
|
coiled sperm flagellum
|
J:271400
|
kinked sperm flagellum
|
J:271400
|
oligozoospermia
|
J:271400
|
teratozoospermia
|
J:271400
|
H2axtm1Fwa/H2ax+
(involves: 129S6/SvEvTac)
|
chromosomal instability
|
J:84879
|
H2axtm1Fwa/H2axtm1Fwa
(involves: 129S6/SvEvTac)
|
chromosomal instability
|
J:84879
|
H2axtm1Nus/H2axtm1Nus
(Not Specified)
|
arrest of male meiosis
|
J:76360
|
decreased cell proliferation
|
J:76360,
J:149487
|
decreased vascular endothelial cell proliferation
|
J:194603
|
increased vascular endothelial cell apoptosis
|
J:149487
|
H2az2Tg(Wnt1-cre)11Rth/H2az2+ Tg(CAG-Bmp4,-EGFP)1Ypc/0
(involves: C57BL/6J * CBA/J * CD-1)
|
enhanced osteoblast differentiation
|
J:214763
|
H2az2Tg(Wnt1-cre)11Rth/H2az2+ Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0
(involves: C57BL/6J * CBA/J * FVB/N)
|
abnormal neural crest cell migration
|
J:153094
|
H2bc21tm1Dlc/H2bc21tm1Dlc
(involves: 129S4/SvJae * C57BL/6)
|
decreased neuron apoptosis
|
J:197878
|
H3f3btm1.1Psk/H3f3btm1.1Psk
(involves: C57BL/6N * FVB/N)
|
abnormal cell cycle
|
J:194593
|
abnormal cell nucleus morphology
|
J:194593
|
abnormal chromosome morphology
|
J:194593
|
polyploidy
|
J:194593
|
H3f4em1Aha/H3f4em1Aha
(Not Specified)
|
abnormal double-strand DNA break repair
|
J:360728
|
azoospermia
|
J:360728
|
decreased male germ cell number
|
J:360728
|
early cellular replicative senescence
|
J:360728
|
oxidative stress
|
J:360728
|
H3f4em1Osb/H3f4em1Osb
(involves: C57BL/6)
|
abnormal male meiosis
|
J:258191
|
abnormal spermatocyte morphology
|
J:258191
|
abnormal spermatogonia morphology
|
J:258191
|
azoospermia
|
J:258191
|
decreased elongated spermatid number
|
J:258191
|
decreased male germ cell number
|
J:258191
|
increased male germ cell apoptosis
|
J:258191
|
H19tm1.1Sriv/H19tm1.1Sriv
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
cellular phenotype
|
J:82595
|
H19tm1.1Sriv/H19tm1Tilg
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal DNA methylation
|
J:82595
|
H19tm1Tilg/H19+
(involves: 129S/SvEv)
|
paternal imprinting
|
J:75054,
J:25091
|
H19tm6Tilg/H19tm6Tilg Tg(Zp3-cre)3Mrt/?
(involves: 129P2/OlaHsd * C57BL/6)
|
genetic imprinting
|
J:57113
|
H19tm7Msb/H19+
(involves: 129P2/OlaHsd * C57BL/6 * M. m. castaneus)
|
cellular phenotype
|
J:118894
|
H19tm7Tilg/H19+
(involves: 129P2/OlaHsd)
|
genetic imprinting
|
J:110857
|
Haaoem1Dunw/Haaoem1Dunw
(involves: C57BL/6N)
|
maternal effect
|
J:272339
|
Hacd2tm1a(EUCOMM)Hmgu/Hacd2tm1a(EUCOMM)Hmgu
(involves: C57BL/6N)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:333944
|
abnormal mitochondrial physiology
|
J:333944
|
abnormal oxidative phosphorylation
|
J:333944
|
Hacd2tm1b(EUCOMM)Hmgu/Hacd2tm1b(EUCOMM)Hmgu
(involves: C57BL/6N)
|
abnormal lipid oxidation
|
J:333944
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:333944
|
abnormal mitochondrial crista morphology
|
J:333944
|
abnormal mitochondrial morphology
|
J:333944
|
abnormal oxidative phosphorylation
|
J:333944
|
dilated mitochondrion
|
J:333944
|
Hadhem1Jgao/Hadhem1Jgao
(Not Specified)
|
abnormal acrosome morphology
|
J:333351
|
abnormal male meiosis
|
J:333351
|
absent sperm head
|
J:333351
|
coiled sperm flagellum
|
J:333351
|
decreased sperm progressive motility
|
J:333351
|
hairpin sperm flagellum
|
J:333351
|
increased male germ cell apoptosis
|
J:333351
|
multinucleated giant male germ cells
|
J:333351
|
oligozoospermia
|
J:333351
|
teratozoospermia
|
J:333351
|
HadhGt(RRM279)Byg/HadhGt(RRM279)Byg
(B6.129P2-HadhGt(RRM279)Byg)
|
abnormal fatty acid oxidation
|
J:179084
|
Hadhatm1Jib/Hadha+
(involves: 129X1/SvJ * NIH Black Swiss)
|
abnormal hepatocyte mitochondrial morphology
|
J:101304
|
Hadhatm1Jib/Hadhatm1Jib
(involves: 129X1/SvJ * NIH Black Swiss)
|
abnormal hepatocyte mitochondrial morphology
|
J:69846
|
Hand1tm1(tTA)Prri/Hand1+ Tg(tetO-Hand1)1Prri/0
(involves: 129/Sv * C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:116090
|
Hand1tm2(Hand1)Abfi/Hand1tm2(Hand1)Abfi
(Not Specified)
|
decreased cell proliferation
|
J:164028
|
Hand1tm2.1(Hand1)Abfi/Hand1tm2.1(Hand1)Abfi
(Not Specified)
|
decreased cell proliferation
|
J:164028
|
Hand1tm5Abfi/Hand1+ Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129S7/SvEvBrd)
|
increased cell death
|
J:311466
|
Hand2tm1.1Majh/Hand2tm1.1Majh H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S1/SvImJ * C57BL/6J * CBA/J * DBA/2)
|
abnormal neuron differentiation
|
J:137726
|
Hand2tm1.1Zllr/Hand2tm1.2Zllr Tg(Prrx1-cre)1Cjt/0
(involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL)
|
abnormal interdigital cell death
|
J:159210
|
increased apoptosis
|
J:159210
|
Hand2tm1.2Zllr/Hand2tm1.2Zllr
(involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 * SJL)
|
increased embryonic tissue cell apoptosis
|
J:159210
|
Hand2tm1Cse/Hand2+ H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S1/Sv * C57BL/6J * CBA/J)
|
abnormal cell cycle
|
J:155265
|
abnormal fetal cardiomyocyte proliferation
|
J:155265
|
Hand2tm1Dsr/Hand2tm1Dsr
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased apoptosis
|
J:49658
|
Hand2tm1Dsr/Hand2tm1Dsr
(involves: 129 * 129S7/SvEvBrd * C57BL/6)
|
increased apoptosis
|
J:169213
|
Hand2tm1Dsr/Hand2tm2.1Dsr Isl1tm1(cre)Tmj/Isl1+
(involves: 129 * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6)
|
increased apoptosis
|
J:169213
|
Hand2os1em1Eno/Hand2os1em1Eno
(C57BL/6-Hand2os1em1Eno)
|
abnormal epigenetic regulation of gene expression
|
J:241318
|
Hap1tm1Xjl/Hap1tm1Xjl
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal vesicle-mediated transport
|
J:213185
|
Hap1tm2Xjl/Hap1tm2Xjl Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129 * C57BL/6 * CBA)
|
abnormal neuron proliferation
|
J:224698
|
impaired neuron differentiation
|
J:224698
|
Hap1tm2Xjl/Hap1tm2Xjl Tg(Camk2a-cre)159Kln/0
(involves: 129S6/SvEvTac * BALB/c * C57BL/6)
|
abnormal neuron proliferation
|
J:224698
|
Hapstr1tm1.1Menm/Hapstr1tm1.2Menm Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: C57BL/6 * C57BL/6J * CBA)
|
decreased fibroblast proliferation
|
J:348964
|
Haspintm1Htan/Haspintm1Htan
(involves: C57BL/6)
|
abnormal male germ cell morphology
|
J:240842
|
Hat1tm1.1Mrpa/Hat1+
(B6.Cg-Hat1tm1.1Mrpa)
|
abnormal double-strand DNA break repair
|
J:296531
|
early cellular replicative senescence
|
J:296531
|
oxidative stress
|
J:296531
|
Hat1tm1.1Mrpa/Hat1tm1.1Mrpa
(involves: C57BL/6J)
|
abnormal mitosis
|
J:199077
|
decreased fibroblast proliferation
|
J:199077
|
Hat1tm1.1Mrpa/Hat1tm1.1Mrpa
(B6.Cg-Hat1tm1.1Mrpa)
|
abnormal double-strand DNA break repair
|
J:296531
|
abnormal mitochondrial physiology
|
J:296531
|
decreased fibroblast proliferation
|
J:296531
|
disorganized mitochondrial cristae
|
J:296531
|
early cellular replicative senescence
|
J:296531
|
increased mitochondrial size
|
J:296531
|
oxidative stress
|
J:296531
|
Haus6tm1.2Sdwb/Haus6tm1.2Sdwb
(B6N(FVB)-Haus6tm1.2Sdwb)
|
abnormal mitotic spindle morphology
|
J:235084
|
Havcr2tm1Bmed/Havcr2tm1Bmed
(B6.Cg-Havcr2tm1Bmed)
|
decreased activation-induced cell death of T cells
|
J:189839
|
decreased T cell proliferation
|
J:189839
|
Hax1tm1Jni/Hax1tm1Jni
(involves: 129P2/OlaHsd * C57BL/6)
|
increased neuron apoptosis
|
J:132627
|
Hba-a1tm1Shs/Hba-a1+
(involves: C57BL/6CrSlc)
|
abnormal aerobic respiration
|
J:81902
|
Hbath-J/Hba+
(B6.Cg-Hbath-J)
|
maternal effect
|
J:29127
|
Hbatm1(HBA)Tow/Hbatm1(HBA)Tow Hbbtm2(HBG1,HBB*)Tow/Hbbtm2(HBG1,HBB*)Tow Slc12a4Rbc10/Slc12a4+
(involves: 129 * BALB/c * C57BL/6J)
|
increased mesangial cell number
|
J:227339
|
Hbb-b1tm1Shs/Hbb-b1+
(involves: C57BL/6CrSlc)
|
abnormal aerobic respiration
|
J:81902
|
Hbbd3th/Hbb+ Tg(LCR-HBA2,LCR-HBB*)1Cos/0
(involves: C57BL/6J * CBA/J * DBA/2J)
|
maternal effect
|
J:94193
|
Hbp1tm1.1Ohts/Hbp1tm1.1Ohts Tg(Nes-cre/ERT2)5-1Imayo/0
(involves: C57BL/6 * CBA/JNCrlj * ICR)
|
abnormal cell cycle
|
J:278919
|
increased neuron apoptosis
|
J:278919
|
Hbs1ltm1a(KOMP)Wtsi/Hbs1ltm1a(KOMP)Wtsi
(C57BL/6NTac-Hbs1ltm1a(KOMP)Wtsi)
|
oligozoospermia
|
J:306384
|
Hbs1ltm1c(KOMP)Wtsi/Hbs1ltm1c(KOMP)Wtsi En1tm2(cre)Wrst/En1+
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6NTac)
|
increased neuronal precursor proliferation
|
J:306384
|
Hcar1tm1Lex/Hcar1tm1Lex
(involves: C57BL/6J)
|
increased retina apoptosis
|
J:282266
|
Hccstm1Tcc/Y Nkx2-5tm2(cre)Rph/Nkx2-5+
(involves: 129S1/Sv)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:143285
|
abnormal respiratory electron transport chain
|
J:143285
|
decreased fetal cardiomyocyte proliferation
|
J:143285
|
Hccstm1Tcc/Hccs+ Nkx2-5tm2(cre)Rph/Nkx2-5+
(involves: 129S1/Sv)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:143285
|
abnormal respiratory electron transport chain
|
J:143285
|
cardiac interstitial fibrosis
|
J:143285
|
Hccstm1Tcc/Hccs+ Nkx2-5tm2(cre)Rph/Nkx2-5+ Tg(CAG-EGFP)D4Nagy/0 Tg(Hmgcr-lacZ)H253Sest/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal fetal cardiomyocyte proliferation
|
J:143285
|
Hcfc1tm1Lwh/Hcfc1+ Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: C57BL/6 * CBA)
|
decreased cell proliferation
|
J:231596
|
increased apoptosis
|
J:231596
|
Hcfc1tm1Lwh/Hcfc1tm1Lwh Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: C57BL/6 * CBA)
|
decreased cell proliferation
|
J:231596
|
increased apoptosis
|
J:231596
|
Hcktm1Hev/Hcktm1Hev
(involves: 129S7/SvEvBrd * C57BL/6J)
|
impaired macrophage phagocytosis
|
J:16994
|
Hcls1tm1Wtn/Hcls1tm1Wtn
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:28146
|
Hcls1tm2Wtn/Hcls1tm2Wtn
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:28146
|
Hcn2trls/Hcn2trls
(Not Specified)
|
azoospermia
|
J:103185
|
Hcsttm1.1Cln/Hcsttm1.1Cln
(B6.129P2-Hcsttm1.1Cln)
|
abnormal osteoclast differentiation
|
J:147155
|
Hdac1tm1.1Eno/Hdac1tm1.1Eno Hdac2tm1.1Eno/Hdac2tm1.1Eno Tg(Myh6-cre)2182Mds/?
(involves: 129S/SvEv * C57BL/6 * CD-1 * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:123173
|
Hdac1tm1.1Eno/Hdac1tm1.1Eno Tg(KRT14-cre)1Ipc/0
(involves: 129S/SvEv * C57BL/6 * SJL)
|
abnormal keratinocyte differentiation
|
J:205733
|
Hdac1tm1.1Mrl/Hdac1tm1.1Mrl Hdac2tm1.1Rdp/Hdac2tm1.1Rdp Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
abnormal mitosis
|
J:197818
|
decreased fibroblast proliferation
|
J:197818
|
early cellular replicative senescence
|
J:197818
|
Hdac1tm1.1Mrl/Hdac1tm1.1Mrl Hdac2tm1.1Rdp/Hdac2tm1.1Rdp Tg(Mx1-cre)1Cgn/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
increased apoptosis
|
J:197818
|
Hdac1tm1.1Pmt/Hdac1tm1.1Pmt
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
decreased cell proliferation
|
J:157903
|
Hdac1tm1.1Pmt/Hdac1tm1.1Pmt Hdac2tm1.1Pmt/Hdac2tm1.1Pmt
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
abnormal cell cycle
|
J:157903
|
increased fibroblast apoptosis
|
J:157903
|
Hdac1tm1.1Pmt/Hdac1tm1.1Pmt Hdac2tm1.1Pmt/Hdac2tm1.1Pmt Cd79atm1(cre)Reth/Cd79a+
(involves: 129P2/OlaHsd * BALB/c * C57BL/6 * FVB/N)
|
increased B cell apoptosis
|
J:157903
|
Hdac1tm1.1Pmt/Hdac1tm1.1Pmt Hdac2tm1.1Pmt/Hdac2tm1.1Pmt Tg(Fcer2a-cre)5Mbu/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N)
|
decreased B cell proliferation
|
J:157903
|
increased B cell apoptosis
|
J:157903
|
Hdac1tm1.1Shmc/Hdac1tm1.1Shmc Hdac2tm1.1Shmc/Hdac2tm1.1Shmc Tg(Lck-cre)1Cwi/0
(involves: 129S7/SvEvBrd)
|
aneuploidy
|
J:194769
|
chromosomal instability
|
J:194769
|
increased T cell proliferation
|
J:194769
|
increased thymocyte apoptosis
|
J:194769
|
trisomy
|
J:194769
|
Hdac1tm1.2Pmt/Hdac1tm1.2Pmt
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
abnormal cell cycle
|
J:157903
|
Hdac2Gt(W035F03)Joe/Hdac2Gt(W035F03)Joe
(Not Specified)
|
increased fetal cardiomyocyte proliferation
|
J:121697
|
Hdac2tm1.1Eem/Hdac2tm1.1Eem Pou5f1tm2Jae/?
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:171358
|
Hdac2tm1.2Eno/Hdac2tm1.2Eno
(involves: 129S/SvEv * C57BL/6 * CD-1)
|
abnormal fetal cardiomyocyte proliferation
|
J:123173
|
increased cardiomyocyte apoptosis
|
J:123173
|
Hdac3tm1.1Eno/Hdac3tm1.1Eno Tg(Myh6-cre)2182Mds/?
(involves: 129S/SvEv * C57BL/6)
|
abnormal cellular respiration
|
J:144604
|
abnormal mitochondrial crista morphology
|
J:144604
|
abnormal myocardial fiber mitochondrial morphology
|
J:144604
|
cardiac interstitial fibrosis
|
J:144604
|
Hdac3tm1Swh/Hdac3tm1.1Swh
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal cell cycle
|
J:134665
|
abnormal cell death
|
J:134665
|
abnormal cell physiology
|
J:134665
|
decreased cell proliferation
|
J:134665
|
Hdac3tm1Swh/Hdac3tm1.1Swh Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * DBA)
|
increased hepatocyte proliferation
|
J:134288
|
Hdac3tm1Swh/Hdac3tm1.1Swh Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N)
|
abnormal cell cycle
|
J:134665
|
abnormal DNA repair
|
J:134665
|
increased fibroblast apoptosis
|
J:134665
|
Hdac6tm1.1Tyao/Hdac6tm1.1Tyao
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal cell migration
|
J:128914
|
Hdac6tm1Anfi/Hdac6tm1Anfi
(Not Specified)
|
cellular phenotype
|
J:234763
|
Hdac8tm1.1Eno/Hdac8tm1.2Eno Tg(Ddx4-cre)1Dcas/0
(involves: 129S6/SvEvTac * C57BL/6J * FVB)
|
abnormal female meiosis
|
J:285736
|
abnormal oocyte morphology
|
J:285736
|
abnormal oogenesis
|
J:285736
|
Hdac8tm1.2Eno/Y
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal chromosome number
|
J:297059
|
abnormal DNA repair
|
J:297059
|
Hdac8tm1.2Eno/Hdac8+
(involves: 129 * C57BL/6 * CD-1)
|
genetic imprinting
|
J:150709
|
Hdgfl2tm1Lex/Hdgfl2tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
decreased fibroblast proliferation
|
J:171883
|
Hecw2tm1.1Fhe/Hecw2tm1.1Fhe
(involves: C57BL/6J)
|
decreased neuronal precursor proliferation
|
J:306367
|
Helbtm1(KOMP)Vlcg/Helbtm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal double-strand DNA break repair
|
J:231089
|
Helbtm1(KOMP)Vlcg/Helbtm1(KOMP)Vlcg Trp53bp1tm1Jc/Trp53bp1tm1Jc
(involves: 129 * C57BL/6NTac)
|
abnormal double-strand DNA break repair
|
J:231089
|
Hellstm1c(EUCOMM)Wtsi/Hellstm1d(EUCOMM)Wtsi Tg(Stra8-icre)1Reb/0
((B6(Cg)-Hellstm1c(EUCOMM)Wtsi/BakrJ x B6.Cg-Hellstm1d(EUCOMM)Wtsi Tg(Stra8-icre)1Reb/Bakr)F1)
|
abnormal DNA methylation
|
J:283594
|
abnormal DNA methylation during gametogenesis
|
J:283594
|
abnormal meiosis
|
J:283594
|
arrest of male meiosis
|
J:283594
|
decreased male germ cell number
|
J:283594
|
increased male germ cell apoptosis
|
J:283594
|
Hellstm1Kmu/Hellstm1Kmu
(involves: 129S/SvEv * CZECHII/EiJ)
|
paternal imprinting
|
J:96925
|
Hellstm1Kmu/Hellstm1Kmu
(involves: 129S1/Sv)
|
abnormal chromosome morphology
|
J:72618
|
increased renal tubule apoptosis
|
J:76112
|
Hellstm1Rarc/Hellstm1Rarc
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal chromosome number
|
J:107145
|
decreased cell proliferation
|
J:107145
|
decreased cellular sensitivity to gamma-irradiation
|
J:107145
|
HelqGt(RRF112)Byg/HelqGt(RRF112)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal spermatogonia morphology
|
J:206104
|
hem6/hem6
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6)
|
asthenozoospermia
|
J:142791
|
teratozoospermia
|
J:142791
|
Henmt1em2Pdz/Henmt1em2Pdz
(C57BL/6J-Henmt1em2Pdz)
|
arrest of male meiosis
|
J:326369
|
Henmt1pin/Henmt1pin
(involves: C57BL/6J * CBA)
|
abnormal manchette morphology
|
J:228973
|
abnormal sperm nucleus morphology
|
J:228973
|
absent sperm mitochondrial sheath
|
J:228973
|
asthenozoospermia
|
J:228973
|
oligozoospermia
|
J:228973
|
pinhead sperm
|
J:228973
|
short sperm flagellum
|
J:228973
|
Herc2Gt(AR0530)Wtsi/Herc2+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal autophagy
|
J:252045
|
abnormal lysosome morphology
|
J:252045
|
Herc2J/Herc2J
(BALB/cJ-Herc2J)
|
abnormal spermatid morphology
|
J:58776
|
decreased male germ cell number
|
J:58776
|
oligozoospermia
|
J:58776
|
Herc4Gt(RRH224)Byg/Herc4Gt(RRH224)Byg
(Not Specified)
|
asthenozoospermia
|
J:128937
|
kinked sperm flagellum
|
J:128937
|
Hes1tm1Fgu/Hes1tm1Fgu
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal neuron differentiation
|
J:30431
|
Hes1tm1Fgu/Hes1tm1Fgu
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell differentiation
|
J:203419
|
Hes1tm1Fgu/Hes1tm1Fgu Hes3tm1Kag/Hes3tm1Kag
(involves: C57BL/6 * CBA * ICR)
|
premature neuronal precursor differentiation
|
J:71074
|
Hes1tm1Fgu/Hes1tm1Fgu Hes3tm1Kag/Hes3tm1Kag Hes5tm1Fgu/Hes5tm1Fgu
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
premature neuronal precursor differentiation
|
J:94391
|
Hes1tm1Fgu/Hes1tm1Fgu Hes5tm1Fgu/Hes5tm1Fgu
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
premature neuronal precursor differentiation
|
J:94391
|
Hes1tm1Kag/Hes1tm1Kag Foxa2tm3.1(icre)Heli/Foxa2+
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal pancreatic beta cell differentiation
|
J:184814
|
Hexblysd/Hexblysd
(B6.Cg-Hexblysd/J)
|
abnormal lysosome morphology
|
J:301674
|
abnormal vacuole morphology
|
J:301674
|
Hexbtm1Rlp/Hexbtm1Rlp
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
increased forebrain apoptosis
|
J:87617
|
Hexim1tm1Maqs/Hexim1tm1Maqs
(involves: 129S/SvEv * Black Swiss)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:92209
|
increased fetal cardiomyocyte apoptosis
|
J:92209
|
Hey1tm1Kkb/Hey1tm1Kkb Heyltm1Kkb/Heyltm1Kkb
(B6.Cg-Hey1tm1Kkb Heyltm1Kkb)
|
abnormal skeletal muscle satellite cell proliferation
|
J:178310
|
Hey2tm1Mtc/Hey2tm1Mtc
(involves: 129X1/SvJ * C57BL/6)
|
cardiac interstitial fibrosis
|
J:80681
|
Hfetm1.1Jrco/Hfe+
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:201948
|
Hfetm1.1Jrco/Hfetm1.1Jrco
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:201948
|
Hfm1Gt(OST347241)Lex/Hfm1Gt(OST347241)Lex
(involves: 129S5/SvEvBrd * C57BL/6 * SJL)
|
abnormal chiasmata formation
|
J:195265
|
abnormal chromosomal synapsis
|
J:195265
|
abnormal meiosis
|
J:195265
|
abnormal meiotic configurations
|
J:195265
|
abnormal oogenesis
|
J:195265
|
abnormal synaptonemal complex
|
J:195265
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:195265
|
arrest of male meiosis
|
J:195265
|
Hgftm1Jmw/Hgftm1Jmw
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased hepatocyte proliferation
|
J:97145
|
Hgftm1Jmw/Hgftm1Jmw Rag2tm1Fwa/Rag2tm1Fwa
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased hepatocyte proliferation
|
J:97145
|
Hgftm1Jmw/Hgftm1Jmw Tg(Mx1-cre)29-4Her/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL)
|
decreased hepatocyte proliferation
|
J:97145
|
Hgstm1Tkh/Hgstm1Tkh
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell physiology
|
J:97764
|
Hgstm2Tkh/Hgstm2Tkh Tg(Syn1-cre)671Jxm/0
(involves: C57BL/6 * CBA * SJL)
|
increased neuron apoptosis
|
J:141391
|
Hgsnattm1a(EUCOMM)Wtsi/Hgsnattm1a(EUCOMM)Wtsi
(involves: C57BL/6N * C57BL/6NTac)
|
abnormal lysosome morphology
|
J:235361
|
abnormal mitochondrial crista morphology
|
J:235361
|
abnormal Purkinje cell mitochondrial morphology
|
J:235361
|
Hhextm1Ngu/Hhextm1Ngu
(involves: 129/Sv * C57BL/6)
|
abnormal monocyte differentiation
|
J:65105
|
Hhextm1Rbe/Hhextm1Rbe
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal hepatoblast migration
|
J:62027
|
Hhiptm1Amc/Hhiptm1Amc
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased pancreatic beta cell proliferation
|
J:85472
|
Hhipl1tm1a(KOMP)Wtsi/Hhipl1tm1a(KOMP)Wtsi
(B6J.B6N-Hhipl1tm1a(KOMP)Wtsi)
|
decreased cell migration
|
J:280707
|
decreased vascular smooth muscle cell proliferation
|
J:280707
|
Hif1atm1Jhu/Hif1atm1Jhu
(involves: 129S4/SvJae * C57BL/6)
|
increased apoptosis
|
J:45554
|
Hif1atm1Pec/Hif1atm1Pec
(involves: 129X1/SvJ * Swiss)
|
abnormal neural crest cell migration
|
J:102537
|
abnormal vascular regression
|
J:102537
|
Hif1atm1Rsjo/Hif1a+
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased neuron apoptosis
|
J:98637
|
Hif1atm1Rsjo/Hif1atm1Rsjo
(involves: 129S1/Sv * 129X1/SvJ)
|
increased embryonic tissue cell apoptosis
|
J:48084
|
Hif1atm1Rsjo/Hif1atm1Rsjo Hif1antm1.2Rsjo/Hif1antm1.2Rsjo
(involves: 129S1/Sv * 129X1/SvJ)
|
cellular phenotype
|
J:160941
|
decreased cell proliferation
|
J:160941
|
Hif1atm1Rsjo/Hif1atm1Rsjo Hif1antm1.2Rsjo/Hif1antm1.2Rsjo Vhltm1Jae/Vhltm1Jae
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
cellular phenotype
|
J:160941
|
Hif1atm2Rsjo/Hif1atm2Rsjo
(involves: 129S1/Sv * 129X1/SvJ)
|
increased embryonic tissue cell apoptosis
|
J:48084
|
Hif1atm3Rsjo/Hif1atm3Rsjo
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:116762
|
decreased hepatocyte proliferation
|
J:152724
|
early cellular replicative senescence
|
J:116762
|
increased cellular sensitivity to gamma-irradiation
|
J:116762
|
Hif1atm3Rsjo/Hif1atm3Rsjo Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+ Hprt1tm1(Pck1-cre)Vhh/Y
(involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ)
|
abnormal cell differentiation
|
J:130751
|
Hif1atm3Rsjo/Hif1atm3Rsjo Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
impaired macrophage chemotaxis
|
J:107682
|
Hif1atm3Rsjo/Hif1atm3Rsjo Tg(Itgax-cre)1-1Reiz/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal cell physiology
|
J:187773
|
abnormal leukocyte migration
|
J:187773
|
Hif1atm3Rsjo/Hif1atm3Rsjo Tg(Pax6-cre,GFP)1Pgr/0
(involves: 129S1/Sv * 129X1/SvJ * FVB)
|
increased lens fiber apoptosis
|
J:141905
|
Hif1atm3Rsjo/Hif1atm3Rsjo Tg(Tek-cre)1Ywa/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal vascular endothelial cell migration
|
J:94773
|
decreased vascular endothelial cell proliferation
|
J:94773
|
Hif1antm1.2Rsjo/Hif1antm1.2Rsjo
(B6.129-Hif1antm1.2Rsjo)
|
abnormal cell physiology
|
J:160941
|
Hint1tm1Ibw/Hint1tm1Ibw
(involves: 129 * C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:84504
|
increased fibroblast proliferation
|
J:84504
|
Hint2tm1.1Geno/Hint2tm1.1Geno
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal hepatocyte mitochondrial morphology
|
J:237329
|
abnormal mitochondrial physiology
|
J:237329
|
abnormal respiratory electron transport chain
|
J:237329
|
oxidative stress
|
J:237329
|
Hip1tm1Tsr/Hip1tm1Tsr
(involves: 129X1/SvJ * C57BL/6)
|
decreased male germ cell number
|
J:72637
|
increased male germ cell apoptosis
|
J:72637
|
multinucleated giant male germ cells
|
J:90400
|
oligozoospermia
|
J:72637
|
Hip1tm3Tsr/Hip1tm3Tsr
(involves: 129X1/SvJ * C57BL/6)
|
abnormal spermatid morphology
|
J:90400
|
Hipk1tm1Hko/Hipk1+ Hipk2tm1Hko/Hipk2tm1Hko
(involves: C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:106931
|
Hipk1tm1Hko/Hipk1tm1Hko
(involves: C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:106931
|
Hipk1tm1Hko/Hipk1tm1Hko Hipk2tm1Hko/Hipk2tm1Hko
(involves: C57BL/6)
|
decreased cell proliferation
|
J:106931
|
increased apoptosis
|
J:106931
|
Hipk2tm1Afus/Hipk2tm1Afus
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell cycle
|
J:156574
|
decreased cell proliferation
|
J:156574
|
Hipk2tm1Ejh/Hipk2tm1Ejh
(involves: 129X1/SvJ * C57BL/6)
|
decreased neuron apoptosis
|
J:117465
|
Hipk2tm1Hko/Hipk2tm1Hko
(involves: C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:106931
|
Hipk3Gt(OST51087)Lex/Hipk3Gt(OST51087)Lex
(involves: 129S5/SvEvBrd)
|
decreased pancreatic beta cell proliferation
|
J:194563
|
Hipk4tm1b(KOMP)Mbp/Hipk4+
(B6N(Cg)-Hipk4tm1b(KOMP)Mbp/J)
|
asthenozoospermia
|
J:290279
|
oligozoospermia
|
J:290279
|
Hipk4tm1b(KOMP)Mbp/Hipk4tm1b(KOMP)Mbp
(B6N(Cg)-Hipk4tm1b(KOMP)Mbp/J)
|
abnormal acroplaxome morphology
|
J:290279
|
abnormal acrosome morphology
|
J:290279
|
abnormal sperm flagellum morphology
|
J:290279
|
abnormal sperm head morphology
|
J:290279
|
abnormal sperm nucleus morphology
|
J:290279
|
abnormal spermatid morphology
|
J:290279
|
asthenozoospermia
|
J:290279
|
coiled sperm flagellum
|
J:290279
|
decreased sperm progressive motility
|
J:290279
|
detached acrosome
|
J:290279
|
enlarged sperm head
|
J:290279
|
increased male germ cell apoptosis
|
J:290279
|
kinked sperm flagellum
|
J:290279
|
oligozoospermia
|
J:290279
|
short sperm flagellum
|
J:290279
|
small sperm head
|
J:290279
|
teratozoospermia
|
J:290279
|
Hivep3tm1Glm/Hivep3tm1Glm
(B6.Cg-Hivep3tm1Glm)
|
abnormal osteoblast physiology
|
J:108965
|
Hivep3tm1Glm/Hivep3tm1Glm
(Not Specified)
|
abnormal osteoclast differentiation
|
J:184764
|
Hivep3tm2Glm/Hivep3tm2Glm
(involves: C57BL/6)
|
abnormal osteoblast physiology
|
J:201597
|
Hk2tm1.1Uku/Hk2tm1.1Uku Tg(GFAP-cre)25Mes/0
(B6.Cg-Hk2tm1.1Uku Tg(GFAP-cre)25Mes)
|
abnormal cerebellar granule cell migration
|
J:210113
|
abnormal neuronal precursor proliferation
|
J:210113
|
Hkdc1tm1a(KOMP)Wtsi/Hkdc1+
(involves: C57BL/6N)
|
decreased cellular glucose uptake
|
J:240354
|
hl/hl
(Not Specified)
|
maternal effect
|
J:30767
|
Hld/Hld
(either: (involves: BALB/cByJ) or (involves: BALB/cJ))
|
abnormal neuronal migration
|
J:13989
|
Hltftm1.1Arte/Hltftm1.1Arte
(Not Specified)
|
abnormal neuronal precursor proliferation
|
J:193813
|
Hltftm1.2Geno/Hltftm1.2Geno
(B6.129S2-Hltftm1.2Geno)
|
increased brain apoptosis
|
J:203735
|
Hmbox1Gt(Ayu21-T346)Imeg/Hmbox1Gt(Ayu21-T346)Imeg
(involves: C57BL/6 * CBA/JNCrlj)
|
abnormal cell morphology
|
J:199000
|
Hmcesem1Dfel/Hmcesem1Dfel
(involves: 129 * C57BL/6N)
|
abnormal DNA methylation
|
J:254234
|
abnormal epigenetic regulation of gene expression
|
J:254234
|
Hmcesem2Dfel/Hmcesem2Dfel
(involves: 129 * C57BL/6N)
|
abnormal DNA methylation
|
J:254234
|
abnormal epigenetic regulation of gene expression
|
J:254234
|
Hmga1tm1Cha/Hmga1+
(chimera involves: 129S1/Sv * C57BL/6J)
|
azoospermia
|
J:84851
|
decreased male germ cell number
|
J:84851
|
Hmga2em1Sson/Hmga2em1Sson
(involves: C57BL/6N)
|
abnormal sperm flagellum morphology
|
J:324153
|
abnormal sperm head morphology
|
J:324153
|
increased male germ cell apoptosis
|
J:324153
|
oligozoospermia
|
J:324153
|
teratozoospermia
|
J:324153
|
Hmga2tm1Cha/Hmga2tm1Cha
(involves: 129S7/SvEvBrd)
|
abnormal spermatogonia morphology
|
J:126188
|
azoospermia
|
J:126188
|
Hmgb1tm1.1Ttg/Hmgb1tm1.1Ttg Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd)
|
impaired macrophage phagocytosis
|
J:205499
|
increased macrophage apoptosis
|
J:205499
|
increased sensitivity to induced cell death
|
J:205499
|
Hmgb1tm1Meb/Hmgb1tm1Meb
(C.129P2-Hmgb1tm1Meb)
|
chromosome breakage
|
J:95963
|
Hmgb2tm1Meb/Hmgb2tm1Meb
(Not Specified)
|
asthenozoospermia
|
J:67968
|
multinucleated giant male germ cells
|
J:67968
|
teratozoospermia
|
J:67968
|
Hmgcltm1Gam/Hmgcltm1Gam
(either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1))
|
abnormal hepatocyte mitochondrial morphology
|
J:52117
|
Hmgcltm2Gam/Hmgcltm2Gam Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(B6.Cg-Hmgcltm2Gam Speer6-ps1Tg(Alb-cre)21Mgn)
|
abnormal hepatocyte mitochondrial morphology
|
J:204294
|
Hmgcs2tm1.1Yil/Hmgcs2tm1.1Yil Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * C3H * C57BL/6 * C57BL/6J)
|
abnormal intestinal crypt stem cell physiology
|
J:280699
|
Hmgcs2tm1.1Yil/Hmgcs2tm1.1Yil Lgr5tm3(cre/ERT2)Cle/Lgr5+ Gt(ROSA)26Sortm9(CAG-tdTomato)Hze/Gt(ROSA)26Sor+
(involves: 129S6/SvEvTac * C3H * C57BL/6J * C57BL/6NCrl)
|
abnormal intestinal crypt stem cell physiology
|
J:280699
|
abnormal jejunal goblet cell morphology
|
J:280699
|
Hmgcs2tm1.1Yil/Hmgcs2tm1.1Yil Tg(Vil1-cre/ERT2)23Syr/0
(involves: C3H * C57BL/6 * C57BL/6J * DBA/2)
|
abnormal jejunal goblet cell morphology
|
J:280699
|
Hmgn1tm1Mbus/Hmgn1+
(involves: 129X1/SvJ)
|
increased cellular sensitivity to gamma-irradiation
|
J:100773
|
Hmgn1tm1Mbus/Hmgn1+
(either: (involves: 129/Sv * 129X1/SvJ) or (involves: 129/Sv * 129X1/SvJ * C57BL/6))
|
increased cellular sensitivity to ultraviolet irradiation
|
J:100282
|
Hmgn1tm1Mbus/Hmgn1tm1Mbus
(either: (involves: 129/Sv * 129X1/SvJ) or (involves: 129/Sv * 129X1/SvJ * C57BL/6))
|
abnormal cell physiology
|
J:100282
|
increased cellular sensitivity to ultraviolet irradiation
|
J:100282
|
Hmgn1tm1Mbus/Hmgn1tm1Mbus
(involves: 129X1/SvJ)
|
abnormal cell cycle checkpoint function
|
J:100773
|
increased cellular sensitivity to gamma-irradiation
|
J:100773
|
increased fibroblast proliferation
|
J:100773
|
Hmmrtm1Plou/Hmmrtm1Plou
(involves: C57BL/6 * C57BL/6J)
|
abnormal meiotic spindle morphology
|
J:221355
|
decreased oocyte number
|
J:221355
|
Hmox1tm1.1Gkl/Hmox1tm1.1Gkl Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129 * 129P2/OlaHsd * BALB/cJ * C57BL/6)
|
increased splenocyte proliferation
|
J:148498
|
Hmox1tm1.1Hes/Hmox1tm1.1Hes Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6J * C57BL/6N)
|
abnormal cellular respiration
|
J:214639
|
abnormal mitochondrial physiology
|
J:214639
|
abnormal redox activity
|
J:214639
|
Hmox1tm1.1Hes/Hmox1tm1.1Hes Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * C57BL/6J * C57BL/6N * DBA)
|
abnormal cellular respiration
|
J:214639
|
abnormal mitochondrial physiology
|
J:214639
|
abnormal redox activity
|
J:214639
|
Hmox1tm1Mlee/Hmox1tm1Mlee
(involves: 129S2/SvPas * BALB/c)
|
increased cardiomyocyte apoptosis
|
J:54684
|
oxidative stress
|
J:54684
|
Hmox1tm1Mlee/Hmox1tm1Mlee
(B6.129S2-Hmox1tm1Mlee)
|
increased vascular smooth muscle cell proliferation
|
J:106600
|
Hmox1tm1Poss/Hmox1tm1Poss
(involves: 129S2/SvPas * C57BL/6)
|
increased renal tubule apoptosis
|
J:62437
|
oxidative stress
|
J:79254
|
Hmx1tm1.1Arte/Hmx1tm1.1Arte H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: BALB/c * C57BL/6J * CBA/J)
|
abnormal neuron differentiation
|
J:198834
|
Hnf1atm1Mya/Hnf1atm1Mya
(involves: 129S2/SvPas)
|
increased hepatocyte proliferation
|
J:31627
|
Hnf1atm2Mya/Hnf1atm2Mya
(involves: 129S2/SvPas)
|
increased hepatocyte proliferation
|
J:31627
|
Hnf4atm1.1Gonz/Hnf4atm1.1Gonz Tg(Alb1-cre)1Dlr/0
(involves: 129X1/SvJ * FVB/N)
|
abnormal hepatocyte mitochondrial morphology
|
J:67396
|
Hnf4atm1Dnl/Hnf4atm1Dnl
(either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6))
|
increased ectoderm apoptosis
|
J:21129
|
Hnf4atm1Dnl/Hnf4atm1Dnl
(involves: 129S4/SvJae * C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:50810
|
Hnrnpa3em1Ionsz/Hnrnpa3em1Ionsz
(C57BL/6J-Hnrnpa3em1Ionsz)
|
abnormal cell cycle
|
J:288307
|
abnormal DNA repair
|
J:288307
|
abnormal mitosis
|
J:288307
|
abnormal neuron differentiation
|
J:288307
|
increased mitotic index
|
J:288307
|
mitotic nondisjunction
|
J:288307
|
HnrnpabGt(AV0462)Wtsi/HnrnpabGt(AV0462)Wtsi
(involves: 129P2/OlaHsd)
|
abnormal neuron differentiation
|
J:227973
|
increased susceptibility to neuronal excitotoxicity
|
J:227973
|
Hnrnph1tm1.1Nju/Hnrnph1tm1.1Nju Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: C57BL/6 * C57BL/6J * C57BL/6N * SJL)
|
abnormal male meiosis
|
J:333262
|
abnormal spermatocyte morphology
|
J:333262
|
decreased spermatid number
|
J:333262
|
increased male germ cell apoptosis
|
J:333262
|
oligozoospermia
|
J:333262
|
Hnrnpktm1.1Cya/Hnrnpktm1.1Cya Tg(Stra8-icre)1Reb/0
(involves: C57BL/6 * FVB/NJ)
|
arrest of male meiosis
|
J:324169
|
increased male germ cell apoptosis
|
J:324169
|
Hnrnpltm1.1Tmo/Hnrnpltm1.1Tmo Tg(Lck-cre)548Jxm/0
(B6.Cg-Hnrnpltm1.1Tmo Tg(Lck-cre)548Jxm)
|
increased T cell proliferation
|
J:188749
|
Hnrnprtm1a(EUCOMM)Wtsi/Hnrnprtm1a(EUCOMM)Wtsi
(C57BL/6-Hnrnprtm1a(EUCOMM)Wtsi)
|
abnormal double-strand DNA break repair
|
J:317395
|
induced chromosome breakage
|
J:317395
|
Hnrnputm1.1Tman/Hnrnputm1.1Tman Tg(Ckmm-cre)5Khn/0
(involves: 129S4/SvJaeSor * FVB)
|
decreased mitochondrial number
|
J:223139
|
increased cardiomyocyte apoptosis
|
J:223139
|
Hoatzem1Seta/Hoatz+
(B6N.Cg-Hoatzem1Seta)
|
abnormal sperm flagellum morphology
|
J:287082
|
Hoatzem1Seta/Hoatzem1Seta
(B6N.Cg-Hoatzem1Seta)
|
abnormal brain ependyma motile cilium physiology
|
J:287082
|
abnormal ependyma motile cilium morphology
|
J:287082
|
abnormal male germ cell morphology
|
J:287082
|
abnormal respiratory motile cilium morphology
|
J:287082
|
abnormal sperm axoneme morphology
|
J:287082
|
abnormal sperm flagellum morphology
|
J:287082
|
asthenozoospermia
|
J:287082
|
decreased brain ependyma motile cilium length
|
J:287082
|
oligozoospermia
|
J:287082
|
short sperm flagellum
|
J:287082
|
teratozoospermia
|
J:287082
|
Hook1azh/Hook1azh
(involves: C57BL/6J * SWR/J)
|
abnormal acrosome morphology
|
J:19242
|
abnormal manchette morphology
|
J:19242
|
abnormal sperm nucleus morphology
|
J:19242
|
abnormal spermatid morphology
|
J:77010,
J:19242,
J:19269
|
absent sperm flagellum
|
J:13990
|
detached sperm flagellum
|
J:77010
|
ectopic manchette
|
J:19242
|
teratozoospermia
|
J:77010,
J:13990
|
Hopxtm1Eno/Hopxtm1Eno
(involves: 129S6/SvEvTac)
|
abnormal fetal cardiomyocyte proliferation
|
J:79152
|
Hormad1tm1.2Atot/Hormad1tm1.2Atot
(involves: 129/Sv * BALB/c * C57BL/6 * SJL)
|
abnormal chiasmata formation
|
J:173089
|
abnormal double-strand DNA break repair
|
J:173089
|
abnormal female meiosis
|
J:173089
|
abnormal male germ cell apoptosis
|
J:173089
|
abnormal male meiosis
|
J:173089
|
abnormal spindle assembly in female meiosis
|
J:173089
|
abnormal synaptonemal complex
|
J:173089
|
azoospermia
|
J:173089
|
impaired polar body extrusion
|
J:173089
|
Hormad1tm1.2Atot/Hormad1tm1.2Atot Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129/Sv * BALB/c * C57BL/6 * SJL)
|
abnormal female meiosis
|
J:173089
|
abnormal male meiosis
|
J:292036,
J:173089
|
abnormal synaptonemal complex
|
J:173089
|
Hormad1tm1Atot/Hormad1tm1Atot
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd)
|
abnormal chiasmata formation
|
J:173089
|
abnormal double-strand DNA break repair
|
J:173089
|
abnormal female meiosis
|
J:173089
|
abnormal male germ cell apoptosis
|
J:173089
|
abnormal male meiosis
|
J:173089
|
abnormal spindle assembly in female meiosis
|
J:173089
|
abnormal synaptonemal complex
|
J:173089
|
azoospermia
|
J:173089
|
impaired polar body extrusion
|
J:173089
|
Hormad1tm1Atot/Hormad1tm1Atot Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd)
|
abnormal female meiosis
|
J:173089
|
abnormal male meiosis
|
J:173089
|
abnormal synaptonemal complex
|
J:173089
|
Hormad1tm1Kura/Hormad1tm1Kura
(either: B6.Cg-Hormad1tm1Kura or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj))
|
abnormal chromosomal synapsis
|
J:213984
|
abnormal DNA repair
|
J:213984
|
abnormal female meiosis
|
J:213984
|
abnormal male germ cell apoptosis
|
J:213984
|
abnormal male meiosis
|
J:213984
|
aneuploidy
|
J:213984
|
arrest of male meiosis
|
J:213984
|
azoospermia
|
J:213984
|
maternal effect
|
J:213984
|
Hormad1tm1Kura/Hormad1tm1Kura Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal female meiosis
|
J:213984
|
abnormal male germ cell apoptosis
|
J:213984
|
abnormal male meiosis
|
J:213984
|
Hormad1tm1Rajk/Hormad1tm1Rajk
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal chiasmata formation
|
J:167522
|
abnormal chromosomal synapsis
|
J:167522
|
abnormal female meiosis I arrest
|
J:167522
|
abnormal meiosis
|
J:167522
|
abnormal spindle assembly in female meiosis
|
J:167522
|
aneuploidy
|
J:167522
|
arrest of male meiosis
|
J:167522
|
azoospermia
|
J:167522
|
increased male germ cell apoptosis
|
J:167522
|
Hormad2tm1.2Atot/Hormad2tm1.2Atot
(involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL)
|
abnormal chiasmata formation
|
J:183982
|
abnormal female meiosis
|
J:183982
|
abnormal male germ cell apoptosis
|
J:183982
|
abnormal male meiosis
|
J:183982
|
Hormad2tm1.2Atot/Hormad2tm1.2Atot Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL)
|
abnormal meiosis
|
J:183982
|
Hormad2tm1Atot/Hormad2tm1Atot
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd)
|
abnormal male germ cell apoptosis
|
J:183982
|
abnormal male meiosis
|
J:183982
|
Hormad2tm1Atot/Hormad2tm1Atot Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6JOlaHsd)
|
abnormal meiosis
|
J:183982
|
Hormad2tm1Kura/Hormad2+ Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal female meiosis
|
J:192634
|
decreased oocyte number
|
J:192634
|
Hormad2tm1Kura/Hormad2tm1Kura
(either: B6.Cg-Hormad2tm1Kura or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj))
|
abnormal female meiosis
|
J:192634
|
abnormal male germ cell apoptosis
|
J:192634
|
abnormal male meiosis
|
J:192634
|
azoospermia
|
J:192634
|
Hormad2tm1Kura/Hormad2tm1Kura Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal female meiosis
|
J:192634
|
Hoxa1tm1Ipc/Hoxa1tm1Ipc Hoxb1tm1Ipc/Hoxb1tm1Ipc
(involves: 129S2/SvPas * 129S7/SvEvBrd)
|
abnormal neural crest cell delamination
|
J:71033
|
abnormal neural crest cell migration
|
J:71033
|
Hoxa1tm1Rez/Hoxa1tm1Rez
(involves: 129S/SvEv * BALB/c * C57BL/6)
|
abnormal cranial neural crest cell migration
|
J:93020
|
Hoxa1tm3.1Mrc/Hoxa1tm3.1Mrc
(involves: 129S1/Sv * 129X1/SvJ)
|
increased hindbrain apoptosis
|
J:41540
|
Hoxa1tm3.1Mrc/Hoxa1tm3.1Mrc Hoxb1tm3Mrc/Hoxb1+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neural crest cell migration
|
J:41540
|
abnormal neuron differentiation
|
J:41540
|
Hoxa1tm3.1Mrc/Hoxa1tm3.1Mrc Hoxb1tm3Mrc/Hoxb1tm3Mrc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neural crest cell migration
|
J:41540
|
abnormal neuron differentiation
|
J:41540
|
increased hindbrain apoptosis
|
J:41540
|
Hoxa2tm1.1Fmr/Hoxa2tm1.1Fmr Tg(CAG-cre/ERT2)F34Fmr/0
(involves: 129 * CD-1)
|
increased oligodendrocyte progenitor number
|
J:193058
|
Hoxa2tm1Ipc/Hoxa2tm1Ipc
(involves: 129S2/SvPas)
|
abnormal neuron differentiation
|
J:54652
|
Hoxa2tm2.1Fmr/Hoxa2tm2.1Fmr
(involves: 129S2/SvPas)
|
increased oligodendrocyte progenitor number
|
J:193058
|
Hoxa2tm2.1Fmr/Hoxa2tm2.1Fmr Hoxb2tm2.2Fmr/Hoxb2tm2.2Fmr
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
decreased oligodendrocyte progenitor number
|
J:193058
|
increased oligodendrocyte progenitor number
|
J:193058
|
Hoxa3tm3Mrc/Hoxa3tm3Mrc Hoxd3tm2Mrc/Hoxd3tm2Mrc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuronal migration
|
J:86041
|
Hoxa5tm1Rob/Hoxa5tm1Rob Pdgfratm11(EGFP)Sor/Pdgfra+
(involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * MF1)
|
abnormal cell migration
|
J:113378
|
Hoxa10tm1Ipc/Hoxa10tm1Ipc
(either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6))
|
azoospermia
|
J:28593
|
Hoxa10tm1Rilm/Hoxa10tm1Rilm
(either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6))
|
azoospermia
|
J:24123
|
Hoxa11tm1Mrc/Hoxa11tm1Mrc Hoxc11tm1Mrc/Hoxc11tm1Mrc Hoxd11tm1Mrc/Hoxd11tm1Mrc
(involves: 129S7/SvEvBrd)
|
increased metanephric mesenchyme apoptosis
|
J:88686
|
Hoxa11tm1Ssp/Hoxa11tm1Ssp
(involves: 129S2/SvPas * CF-1)
|
azoospermia
|
J:25252
|
increased male germ cell apoptosis
|
J:25252
|
Hoxa11osem1Kaf/Hoxa11osem1Kaf
(C57BL/6-Hoxa11osem1Kaf)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:344661
|
abnormal mitochondrial crista morphology
|
J:344661
|
abnormal mitochondrial matrix morphology
|
J:344661
|
abnormal mitochondrial morphology
|
J:344661
|
abnormal mitochondrial physiology
|
J:344661
|
abnormal oxidative phosphorylation
|
J:344661
|
decreased mitochondrial DNA content
|
J:344661
|
decreased mitochondrial size
|
J:344661
|
dilated mitochondrion
|
J:344661
|
oxidative stress
|
J:344661
|
Hoxb1tm1(cre)Og/Hoxb1+ Pbx3tm1Og/Pbx3tm1Og
(involves: 129S/SvEv * 129S4/SvJae * C57BL/6)
|
abnormal neuron differentiation
|
J:130927
|
Hoxb1tm1Brd/Hoxb1tm1Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal axon guidance
|
J:37450
|
abnormal neuron differentiation
|
J:37450
|
Hoxb1tm1Mrc/Hoxb1tm1Mrc
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuron differentiation
|
J:36235
|
Hoxb1tm2Brd/Hoxb1tm2Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal axon guidance
|
J:37450
|
abnormal neuron differentiation
|
J:37450
|
Hoxb1tm2Mrc/Hoxb1tm2Mrc
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuron differentiation
|
J:36235
|
Hoxb2tm2.2Fmr/Hoxb2tm2.2Fmr
(involves: C57BL/6 * SJL)
|
decreased oligodendrocyte progenitor number
|
J:193058
|
Hoxb3osem1Kabo/Hoxb3osem1Kabo
(C57BL/6J-Hoxb3osem1Kabo)
|
increased kidney cell proliferation
|
J:345935
|
Hoxb3osem1Kabo/Hoxb3osem1Kabo Pkd1tm1.1Pcha/Pkd1tm1.1Pcha
(involves: 129 * C57BL/6J)
|
increased kidney cell proliferation
|
J:345935
|
Hoxb3osem1Kabo/Hoxb3osem1Kabo Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Pkhd1-cre)1Igr/0
(involves: 129S4/SvJae * C57BL/6J)
|
increased kidney cell proliferation
|
J:345935
|
Hoxb13tm1Mrc/Hoxb13tm1Mrc
(Not Specified)
|
abnormal neuron differentiation
|
J:82849
|
Hoxb13tm2Mrc/Hoxb13tm2Mrc
(Not Specified)
|
abnormal neuron differentiation
|
J:82849
|
Hoxb13tm3Mrc/Hoxb13tm3Mrc
(Not Specified)
|
abnormal neuron differentiation
|
J:82849
|
Hoxb13tm4Mrc/Hoxb13tm4Mrc
(Not Specified)
|
abnormal neuron differentiation
|
J:82849
|
Hoxd9tm1Emca/Hoxd9tm1Emca Hoxd10tm1Emca/Hoxd10tm1Emca
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal axon fasciculation
|
J:59070
|
Hp1bp3tm1a(EUCOMM)Wtsi/Hp1bp3tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
cellular phenotype
|
J:223832
|
Hptm1Alev/Hptm1Alev
(involves: 129 * C57BL/6)
|
decreased cholesterol efflux
|
J:129061
|
Hpcatm1Toho/Hpcatm1Toho
(involves: 129S/SvEv * C57BL/6)
|
increased susceptibility to neuronal excitotoxicity
|
J:97752
|
Hpdlem1Jgg/Hpdlem1Jgg
(C57BL/6-Hpdlem1Jgg)
|
increased neuron apoptosis
|
J:334229
|
Hpgdtm1Bhk/Hpgdtm1Bhk
(involves: 129P2/OlaHsd)
|
abnormal vascular regression
|
J:74466
|
patent ductus arteriosus
|
J:74466
|
Hprt1b-m3/Y Impdh1tm1Bmi/Impdh1tm1Bmi
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased splenocyte proliferation
|
J:85443
|
decreased T cell proliferation
|
J:85443
|
Hprt1tm1(ACTB-Opa1)Lsc/Y
(involves: 129 * C57BL/6 * C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:214492
|
abnormal mitochondrial physiology
|
J:214492
|
Hprt1tm1(CAG-BRF1)Gu/Hprt1+ Krastm4Tyj/Kras+ Trp53tm2Tyj/Trp53+ Tg(Pdx1-cre)6Tuv/0
(involves: 129P2/OlaHsd * 129S4/SvJae * 129S7/SvEvBrd * FVB/N)
|
abnormal translation
|
J:285667
|
Hprt1tm1(CAG-Gys1*)Jjg/? Myl1tm1(cre)Sjb/Myl1+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
abnormal cellular respiration
|
J:244440
|
Hprt1tm1(CAG-Gys1*)Jjg/? Tg(Nes-cre)1Kag/?
(involves: 129P2/OlaHsd)
|
impaired autophagy
|
J:210491
|
Hprt1tm1(CAG-NRIP1)Vcls/Y
(involves: 129 * C57BL/6)
|
abnormal enterocyte proliferation
|
J:211324
|
decreased enterocyte apoptosis
|
J:211324
|
Hprt1tm1(CAG-NRIP1)Vcls/Hprt1+
(involves: 129 * C57BL/6)
|
abnormal enterocyte proliferation
|
J:211324
|
decreased enterocyte apoptosis
|
J:211324
|
Hprt1tm1(MAPT)Dph/Y
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal autophagy
|
J:263643
|
Hprt1tm1(Nphs1-CMIP)Dsah/Hprt1+
(B6.Cg-Hprt1tm1(Nphs1-CMIP)Dsah)
|
increased mesangial cell number
|
J:185411
|
Hprt1tm1(Pck1-cre)Vhh/Hprt1+ Tg(CAG-lacZ,-Miox)#Ysk/0
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased renal tubule apoptosis
|
J:266834
|
oxidative stress
|
J:266834
|
Hprt1tm1(Rcan1)Zyga/Hprt1+
(B6.129P2-Hprt1tm1(Rcan1)Zyga)
|
decreased vascular endothelial cell proliferation
|
J:150286
|
Hprt1tm1(UBC-UBB)Rrk/Y Ubctm1Rrk/Ubctm1Rrk
(involves: 129 * C57BL/6J)
|
cellular phenotype
|
J:122574
|
Hprt1tm1(UBC-UBB)Rrk/Hprt1tm1(UBC-UBB)Rrk Ubctm1Rrk/Ubctm1Rrk
(involves: 129 * C57BL/6J)
|
cellular phenotype
|
J:122574
|
Hprt1tm1.1(CAG-Smpd1)Jhkh/Hprt1+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuron differentiation
|
J:199833
|
Hprt1tm2(CAG-Ppp1r3c)Jjg/?
(Not Specified)
|
impaired autophagy
|
J:210491
|
Hprt1tm2(CAG-Ppp1r3c)Jjg/? Nhlrc1tm1(KOMP)Vlcg/Nhlrc1tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
impaired autophagy
|
J:210491
|
Hprt1tm4(CAG-Tbx18*,-Venus)Akis/Y Tbx18tm4(cre)Akis/Tbx18+
(involves: 129S1/SvImJ * NMRI)
|
decreased fetal cardiomyocyte proliferation
|
J:210076
|
Hprt1tm4(Tek-IGF1R)Geno/Y
(B6.129P2-Hprt1tm4(Tek-IGF1R)Geno)
|
abnormal vascular endothelial cell migration
|
J:208523
|
Hprt1tm86(NR2E1,bEMS223)Ems/Y
(B6.Cg-Hprt1tm86(NR2E1,bEMS223)Ems)
|
abnormal neuronal precursor proliferation
|
J:183689
|
Hprt1tm86(NR2E1,bEMS223)Ems/Y Nr2e1frc/Nr2e1frc
(involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:183689
|
Hps1ep/Hps1ep
(involves: C3HeB/FeJ * C57BL/6J)
|
decreased platelet ATP level
|
J:7327
|
Hps1ep/Hps1ep
(B6.C3Fe-Hps1ep/J)
|
abnormal lysosome physiology
|
J:6801
|
decreased platelet ATP level
|
J:7327
|
increased lysosomal enzyme secretion
|
J:7327
|
Hps3coa/Hps3coa
(involves: C57BL/10J)
|
decreased platelet ATP level
|
J:9300
|
Hps4le/Hps4le
(B6.C3-Pde6brd1 Hps4le)
|
decreased lysosomal enzyme secretion
|
J:61552,
J:5967
|
increased lysosomal enzyme secretion
|
J:7327
|
Hps5ru2-mr/Hps5ru2-mr
(B6.Cg-Hps5ru2-mr/Re)
|
decreased platelet ATP level
|
J:7327
|
Hpsetm1.2Mdh/Hpsetm1.2Mdh
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal dendritic cell chemotaxis
|
J:209913
|
Hrhr/Hrhr
(HRS/J)
|
decreased T cell proliferation
|
J:6375
|
Hrhr/Hrhr Ptgs1tm1Unc/Ptgs1+
(involves: 129P2/OlaHsd * C57BL/6 * SKH1)
|
increased cell proliferation
|
J:121635
|
Hrhr/Hrhr Ptgs2tm1Unc/Ptgs2+
(involves: 129P2/OlaHsd * C57BL/6 * SKH1)
|
increased cell proliferation
|
J:121635
|
Hrhr/Hrhr Tg(KRT14-Ptgs2)1Sumf/0
(involves: C57BL/6 * DBA/2 * FVB/N * SKH1)
|
decreased cell proliferation
|
J:121635
|
Hrrhsl/Hrrhsl
(involves: BALB/c)
|
abnormal keratinocyte differentiation
|
J:98859
|
Hrh1tm1Wtn/Hrh1tm1Wtn
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:111704
|
decreased T cell proliferation
|
J:111704
|
Hrktm1Ast/Hrktm1Ast
(C57BL/6-Hrktm1Ast)
|
decreased neuron apoptosis
|
J:124044
|
Hrktm1Nnz/Hrktm1Nnz
(involves: 129 * C57BL/6J)
|
decreased neuron apoptosis
|
J:96893
|
Hs6st1tm1Kkm/Hs6st1tm1Kkm Hs6st2tm1.1Kkm/Hs6st2tm1.1Kkm
(involves: 129P2/OlaHsd)
|
decreased cell proliferation
|
J:136555
|
Hsd11b1tm1a(KOMP)Wtsi/Hsd11b1+
(involves: C57BL/6Jcl * C57BL/6N)
|
increased fibroblast proliferation
|
J:214146
|
Hsd11b1tm1a(KOMP)Wtsi/Hsd11b1tm1a(KOMP)Wtsi
(involves: C57BL/6Jcl * C57BL/6N)
|
abnormal fibroblast proliferation
|
J:214146
|
increased fibroblast proliferation
|
J:214146
|
Hsd11b2tm1Yko/Hsd11b2tm1Yko
(involves: 129P2/OlaHsd * MF1)
|
abnormal fetal cardiomyocyte proliferation
|
J:53391
|
Hsd17b4tm1Baes/Hsd17b4tm1Baes
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal male germ cell morphology
|
J:108368
|
abnormal spermatid morphology
|
J:108368
|
Hsd17b7tm1Mpo/Hsd17b7tm1Mpo
(involves: 129S7/SvEvBrd)
|
increased neural tube apoptosis
|
J:160004
|
Hsd17b12Gt(A030E06)Wrst/Hsd17b12+
(involves: 129S2/SvPas * C57BL/6N)
|
abnormal cell physiology
|
J:160025
|
Hsd17b12Gt(A030E06)Wrst/Hsd17b12Gt(A030E06)Wrst
(involves: 129S2/SvPas * C57BL/6N)
|
decreased inner cell mass proliferation
|
J:160025
|
Hsd17b13tm1Lex/Hsd17b13tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6N)
|
decreased fatty acid beta-oxidation
|
J:273927
|
Hsd17b14tm1Lex/Hsd17b14tm1Lex
(B6;129S5-Hsd17b14tm1Lex/Mmucd)
|
oligozoospermia
|
J:171883
|
Hsf1tm1.1Echr/Hsf1tm1.1Echr Tg(Zp3-cre)93Knw/0
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal female meiosis
|
J:175085
|
abnormal meiotic spindle assembly checkpoint
|
J:175085
|
Hsf1tm1Ijb/Hsf1tm1Ijb
(involves: 129S6/SvEvTac)
|
abnormal chromosomal synapsis
|
J:175085
|
abnormal female meiosis
|
J:175085
|
abnormal meiotic spindle assembly checkpoint
|
J:175085
|
abnormal synaptonemal complex
|
J:175085
|
Hsf1tm1Miv/Hsf1tm1Miv
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell death
|
J:88534
|
decreased sensitivity to induced cell death
|
J:88534
|
Hsf1tm1Miv/Hsf1tm1Miv Hsf2tm1Miv/Hsf2tm1Miv
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
arrest of male meiosis
|
J:88035
|
azoospermia
|
J:88035
|
multinucleated giant male germ cells
|
J:88035
|
Hsf2tm1Miv/Hsf2tm1Miv
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
decreased male germ cell number
|
J:88035
|
oligozoospermia
|
J:88035,
J:83730
|
Hsf2tm1Mmr/Hsf2tm1Mmr
(involves: 129S2/SvPas * C57BL/6)
|
abnormal female germ cell morphology
|
J:76942
|
abnormal male germ cell apoptosis
|
J:76942
|
abnormal male meiosis
|
J:76942
|
abnormal synaptonemal complex
|
J:76942
|
decreased oocyte number
|
J:76942
|
maternal effect
|
J:76942
|
oligozoospermia
|
J:76942
|
Hsf2bpem1Amp/Hsf2bpem1Amp
(involves: C57BL/6J * CBA/J)
|
abnormal chromosomal synapsis
|
J:303558
|
abnormal DNA repair
|
J:303558
|
abnormal female meiosis
|
J:303558
|
abnormal spermatocyte morphology
|
J:303558
|
azoospermia
|
J:303558
|
Hsf2bpem1Roka/Hsf2bpem1Roka
(C57BL/6JOlaHsd-Hsf2bpem1Roka)
|
abnormal chromosomal synapsis
|
J:294372
|
abnormal male meiosis
|
J:294372
|
abnormal spermatocyte morphology
|
J:294372
|
azoospermia
|
J:294372
|
Hsf2bpem2Amp/Hsf2bpem2Amp
(involves: C57BL/6J * CBA/J)
|
abnormal DNA repair
|
J:303558
|
abnormal male meiosis
|
J:303558
|
abnormal meiosis
|
J:303558
|
oligozoospermia
|
J:303558
|
Hsf2bptm1b(EUCOMM)Hmgu/Hsf2bptm1b(EUCOMM)Hmgu
(involves: C57BL/6N)
|
abnormal double-strand DNA break repair
|
J:292036
|
Hsf5em1Asla/Hsf5em1Asla
(Not Specified)
|
abnormal male meiosis
|
J:352587
|
arrest of male meiosis
|
J:352587
|
azoospermia
|
J:352587
|
increased male germ cell apoptosis
|
J:352587
|
Hsh2dtm1Viss/Hsh2dtm1Viss
(B6.129-Hsh2dtm1Viss)
|
increased T cell proliferation
|
J:111408
|
Hsp90aa1Gt(XE444)Byg/Hsp90aa1Gt(XE444)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:169871
|
abnormal male meiosis
|
J:169871
|
arrest of male meiosis
|
J:169871
|
azoospermia
|
J:169871
|
Hsp90aa1Tg(Tyr)2396BOve/Hsp90aa1Tg(Tyr)2396BOve
(involves: C57BL/6 * FVB/N * FVB/NJ)
|
abnormal photoreceptor connecting cilium morphology
|
J:283232
|
increased retina apoptosis
|
J:283232
|
Hsp90aa1tm1.1Udon/Hsp90aa1tm1.1Udon
(involves: C57BL/6 * FVB)
|
azoospermia
|
J:187954
|
increased male germ cell apoptosis
|
J:187954
|
Hsp90aa1tm1.2Udon/Hsp90aa1tm1.2Udon Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: C57BL/6 * C57BL/6NTac * FVB/N)
|
abnormal male germ cell apoptosis
|
J:187954
|
azoospermia
|
J:187954
|
Hsp90b1tm1Yarg/Hsp90b1tm1Yarg
(B6.129X1-Hsp90b1tm1Yarg)
|
abnormal cell differentiation
|
J:146397
|
Hsp90b1tm1Zhli/Hsp90b1tm1.1Zhli Tg(Ddx4-cre)1Dcas/0
(involves: 129S/SvEv * FVB)
|
abnormal acrosome morphology
|
J:168319
|
abnormal sperm head morphology
|
J:168319
|
abnormal sperm midpiece morphology
|
J:168319
|
asthenozoospermia
|
J:168319
|
enlarged sperm head
|
J:168319
|
globozoospermia
|
J:168319
|
Hspa1atm1.1Msk/Hspa1atm1.1Msk
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:72943
|
Hspa1atm1Msk/Hspa1a+
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:72943
|
Hspa1atm1Msk/Hspa1atm1Msk
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:72943
|
increased sensitivity to induced cell death
|
J:72943
|
Hspa1btm1.1Msk/Hspa1btm1.1Msk
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:72943
|
Hspa1btm1Jss/Hspa1btm1Jss
(involves: C57BL/6)
|
increased cellular sensitivity to oxidative stress
|
J:97232
|
increased kidney apoptosis
|
J:97232
|
Hspa1btm1Msk/Hspa1b+
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:72943
|
Hspa1btm1Msk/Hspa1btm1Msk
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:72943
|
increased sensitivity to induced cell death
|
J:72943
|
Hspa2tm1Dix/Hspa2tm1Dix
(either: 129S/SvEv or C57BL/6)
|
abnormal male meiosis
|
J:35110
|
Hspa4tm1Imad/Hspa4tm1Imad
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal spermatid morphology
|
J:180915
|
abnormal spermatocyte morphology
|
J:180915
|
arrest of male meiosis
|
J:180915
|
asthenozoospermia
|
J:180915
|
decreased elongated spermatid number
|
J:180915
|
decreased round spermatid number
|
J:180915
|
increased male germ cell apoptosis
|
J:180915
|
oligozoospermia
|
J:180915
|
Hspa4ltm1Imad/Hspa4ltm1Imad
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
asthenozoospermia
|
J:114659
|
oligozoospermia
|
J:114659
|
Hspa5baffled/Hspa5baffled
(FVB.Cg-Hspa5baffled)
|
abnormal axon extension
|
J:191772
|
abnormal axon fasciculation
|
J:191772
|
abnormal neuron differentiation
|
J:191772
|
abnormal neuron proliferation
|
J:191772
|
Hspa5baffled/Hspa5baffled Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw
(involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal axon extension
|
J:168258
|
abnormal axon fasciculation
|
J:168258
|
Hspa5tm1.1Alee/Hspa5tm1.1Alee
(involves: 129 * C57BL/6 * FVB/N)
|
abnormal inner cell mass apoptosis
|
J:111416
|
absent inner cell mass proliferation
|
J:111416
|
Hspb1tm1.1Jdn/Hspb1tm1.1Jdn
(B6.129S2(Cg)-Hspb1tm1.1Jdn)
|
abnormal cell cycle
|
J:209117
|
decreased fibroblast proliferation
|
J:209117
|
Hspb2tm1.1Ijb/Hspb2tm1.1Ijb
(involves: 129S4/SvJaeSor * FVB)
|
abnormal cellular respiration
|
J:189659
|
abnormal mitochondrial physiology
|
J:189659
|
Hspb6em1Cya/Hspb6em1Cya
(C57BL/6J-Hspb6em1Cya/Cya)
|
increased apoptosis
|
J:347876
|
Hspb7tm1.2Chen/Hspb7tm1.2Chen
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased fetal cardiomyocyte proliferation
|
J:256653
|
Hspb8tm1.1Depr/Hspb8tm1.1Depr
(B.129-Hspb8tm1.1Depr)
|
abnormal cellular respiration
|
J:186292
|
Hspb8tm1Vti/Hspb8tm1Vti
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl)
|
impaired autophagy
|
J:284796
|
Hspbp1tm1Jhoh/Hspbp1tm1Jhoh
(B6.129P2-Hspbp1tm1Jhoh)
|
arrest of male meiosis
|
J:216246
|
azoospermia
|
J:216246
|
decreased elongated spermatid number
|
J:216246
|
decreased male germ cell number
|
J:216246
|
decreased round spermatid number
|
J:216246
|
decreased spermatid number
|
J:216246
|
increased male germ cell apoptosis
|
J:216246
|
Hspd1Gt(OST171441)Lex/Hspd1+
(B6.129S5-Hspd1Gt(OST171441)Lex)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:197946
|
abnormal mitochondrial morphology
|
J:197946
|
disorganized mitochondrial cristae
|
J:197946
|
Hspd1tm1c(EUCOMM)Hmgu/Hspd1tm1c(EUCOMM)Hmgu A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: Black Swiss * C57BL/6 * C57BL/6N * FVB/N)
|
abnormal mitochondrial physiology
|
J:283049
|
oxidative stress
|
J:283049
|
Hspg2tm1Nid/Hspg2tm1Nid
(involves: 129X1/SvJ * C57BL/6)
|
decreased chondrocyte proliferation
|
J:67299
|
Hspg2tm1Rdgr/Hspg2tm1Rdgr
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:121855
|
Hspg2tm1Ref/Hspg2tm1Ref
(involves: 129S1/Sv * 129X1/SvJ)
|
impaired basement membrane formation
|
J:58700
|
Hspg2tm1Ref/Hspg2tm1Ref
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal basement membrane morphology
|
J:119018
|
abnormal radial glial cell endfoot morphology
|
J:119018
|
Hsph1tm1Kzn/Hsph1tm1Kzn
(B6.129P2-Hsph1tm1Kzn)
|
abnormal cell physiology
|
J:218516
|
Hstx1PWD/Ph/Y
(involves: C57BL/6J * PWD/Ph)
|
oligozoospermia
|
J:92309
|
teratozoospermia
|
J:92309
|
Htatip2tm1Hx/Htatip2+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:87066
|
increased fibroblast proliferation
|
J:87066
|
Htatip2tm1Hx/Htatip2tm1Hx
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:87066
|
increased fibroblast proliferation
|
J:87066
|
Htr1btm1Rhn/Htr1btm1Rhn
(involves: 129S2/SvPas)
|
increased osteoblast proliferation
|
J:146078
|
Htr2btm1Kry/Htr2btm1Kry Tg(Ins2-cre)23Herr/0
(involves: C57BL/6J * CBA/J)
|
decreased pancreatic beta cell proliferation
|
J:284574
|
Htr2btm1Lum/Htr2btm1Lum
(129S2/SvPas-Htr2btm1Lum)
|
abnormal fetal cardiomyocyte proliferation
|
J:64067
|
Htra2tm1.1Hohj/Htra2tm1.1Hohj Tg(Nes-cre)1Kln/0
(involves: C57BL/6J)
|
abnormal mitochondrial morphology
|
J:225666
|
abnormal respiratory electron transport chain
|
J:225666
|
increased brain apoptosis
|
J:225666
|
Htra2tm1.2Hohj/Htra2tm1.2Hohj
(involves: C57BL/6 * C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:225666
|
abnormal mitochondrial inner membrane morphology
|
J:225666
|
abnormal mitochondrial morphology
|
J:225666
|
abnormal respiratory electron transport chain
|
J:225666
|
dilated mitochondrion
|
J:225666
|
increased brain apoptosis
|
J:225666
|
Htra2tm1Jdo/Htra2tm1Jdo
(involves: 129P/Ola * C57BL/6)
|
abnormal mitochondrial morphology
|
J:94227
|
increased apoptosis
|
J:94227
|
increased susceptibility to neuronal excitotoxicity
|
J:94227
|
Htra2tm1Jdo/Htra2tm1Jdo Diablotm1Mak/Diablotm1Mak
(involves: 129P/Ola * C57BL/6)
|
increased apoptosis
|
J:94227
|
Htttm1Hay/Htttm1Hay Tg(YAC72)2511Hay/0
(involves: FVB/N)
|
abnormal male germ cell apoptosis
|
J:67366
|
abnormal spermatid morphology
|
J:67366
|
multinucleated giant male germ cells
|
J:67366
|
oligozoospermia
|
J:67366
|
Htttm1Mem/Htttm1Mem
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
|
increased ectoderm apoptosis
|
J:27183
|
Htttm1Szi/Htttm1Szi
(either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * MF1))
|
increased embryonic epiblast cell apoptosis
|
J:29267
|
increased embryonic tissue cell apoptosis
|
J:29267
|
Htttm1Szi/Htttm2Szi Tg(Camk2a-cre)1Szi/0
(involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA)
|
oligozoospermia
|
J:65520
|
Htttm1Szi/Htttm2Szi Tg(Camk2a-cre)2Szi/0
(involves: 129S/SvEv * 129S1/Sv * C57BL/6 * CBA)
|
oligozoospermia
|
J:65520
|
Htttm3Szi/Htttm3Szi
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:106763
|
abnormal cell physiology
|
J:106763
|
abnormal cell proliferation
|
J:106763
|
decreased cell proliferation
|
J:106763
|
Htttm5Mem/Htt+ Mtmr10em1Mem/Mtmr10em1Mem
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:298297
|
Htttm5Mem/Htt+ Rrm2bem1Mem/Rrm2b+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
cellular phenotype
|
J:298297
|
Htttm5Mem/Htt+ Ubr5em1Mem/Ubr5+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:298297
|
Htttm5Mem/Htt+ Ubr5em2Mem/Ubr5em2Mem
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell physiology
|
J:298297
|
hubb/hubb
(involves: ICR)
|
azoospermia
|
J:8170
|
Hus1tm1.1Rsw/Hus1tm1.1Rsw
(involves: 129S4/SvJaeSor * 129S6/SvEvTac)
|
increased embryonic tissue cell apoptosis
|
J:99339
|
Hus1tm1Led/Hus1tm1Led
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss))
|
absent fibroblast proliferation
|
J:63869
|
chromosome breakage
|
J:63869
|
increased embryonic tissue cell apoptosis
|
J:63869
|
Hus1tm1Led/Hus1tm1Led
(involves: 129S6/SvEvTac)
|
increased embryonic tissue cell apoptosis
|
J:99339
|
Hus1tm1Led/Hus1tm2Rsw
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:118898
|
abnormal cell physiology
|
J:118898
|
abnormal chromosome morphology
|
J:118898
|
chromosome breakage
|
J:118898
|
decreased cell proliferation
|
J:118898
|
induced chromosome breakage
|
J:118898
|
oxidative stress
|
J:118898
|
Huwe1tm1Alas/Y Tg(Nes-cre)1Kag/0
(involves: 129S7/SvEvBrd)
|
abnormal neuronal precursor proliferation
|
J:152966
|
Huwe1tm1Alas/Y Tg(Spo11-cre)1Rsw/0
(involves: 129S7/SvEvBrd)
|
abnormal spermatocyte morphology
|
J:323709
|
Huwe1tm1Alas/Y Tg(Stra8-icre)1Reb/0
(involves: 129S7/SvEvBrd * C57BL/6 * FVB/NJ)
|
abnormal male germ cell physiology
|
J:323709
|
abnormal male meiosis
|
J:323709
|
abnormal spermatocyte morphology
|
J:323709
|
abnormal spermatogonia morphology
|
J:323709
|
decreased male germ cell number
|
J:323709
|
increased male germ cell apoptosis
|
J:323709
|
increased testis apoptosis
|
J:323709
|
oligozoospermia
|
J:323709
|
Hydinhy3-Tg(Bdnf)459Ove/Hydinhy3-Tg(Bdnf)459Ove
(FVB/N-Hydinhy3-Tg(Bdnf)459Ove)
|
abnormal brain ependyma motile cilium morphology
|
J:135322
|
abnormal brain ependyma motile cilium physiology
|
J:135322
|
abnormal respiratory motile cilium physiology
|
J:135322
|
Hydinhy3/Hydinhy3
(involves: FVB/N)
|
abnormal ependyma motile cilium morphology
|
J:135322
|
abnormal respiratory motile cilium morphology
|
J:135322
|
abnormal respiratory motile cilium physiology
|
J:135322
|
Hyou1tm1Oga/Hyou1+
(involves: 129S1/Sv * C57BL/6)
|
increased susceptibility to neuronal excitotoxicity
|
J:91396
|
Ica1tm1Mdos/Ica1tm1Mdos Ica1lem1Jxia/Ica1lem1Jxia
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal acrosome morphology
|
J:233657
|
abnormal sperm mitochondrial sheath morphology
|
J:233657
|
abnormal sperm nucleus morphology
|
J:233657
|
absent acrosome
|
J:233657
|
globozoospermia
|
J:233657
|
oligozoospermia
|
J:233657
|
Ica1lem1Jxia/Ica1lem1Jxia
(involves: C57BL/6 * CBA)
|
abnormal sperm mitochondrial sheath morphology
|
J:233657
|
abnormal sperm nucleus morphology
|
J:233657
|
globozoospermia
|
J:233657
|
oligozoospermia
|
J:233657
|
Icam1tm1Alb/Icam1tm1Alb
(B6.Cg-Icam1tm1Alb)
|
abnormal leukocyte adhesion
|
J:100242
|
abnormal leukocyte tethering or rolling
|
J:100242
|
Icam1tm1Bay/Icam1tm1Bay
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal cellular extravasation
|
J:14565
|
Icam1tm1Bay/Icam1tm1Bay
(B6.129S7-Icam1tm1Bay)
|
abnormal cell migration
|
J:118196
|
abnormal cell physiology
|
J:118196
|
abnormal cellular extravasation
|
J:48271
|
abnormal leukocyte migration
|
J:24239
|
abnormal leukocyte tethering or rolling
|
J:48271
|
Icam1tm1Bay/Icam1tm1Bay
(either: B6.129S7-Icam1tm1Bay or (involves: 129S7/SvEvBrd * C57BL/6))
|
abnormal leukocyte tethering or rolling
|
J:31374
|
Icam1tm1Bay/Icam1tm1Bay Seletm2Alb/Seletm2Alb Selptm1Bay/Selptm1Bay
(involves: 129S7/SvEvBrd * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:112286
|
Icam1tm1Bay/Icam1tm1Bay Selltm1Tft/Selltm1Tft
(B6.129-Selltm1Tft Icam1tm1Bay)
|
abnormal cellular extravasation
|
J:48271
|
abnormal leukocyte tethering or rolling
|
J:48271
|
decreased keratinocyte migration
|
J:124291
|
impaired macrophage chemotaxis
|
J:124291
|
Icam1tm1Bay/Icam1tm1Bay Selptm1Bay/Selptm1Bay
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal leukocyte migration
|
J:24239
|
Icam1tm1Bay/Icam1tm1Bay Selptm1Bay/Selptm1Bay
(either: B6.129S7-Selptm1Bay Icam1tm1Bay or (involves: 129S7/SvEvBrd * C57BL/6))
|
impaired leukocyte tethering or rolling
|
J:31374
|
Icam1tm1Jcgr/Icam1tm1Jcgr Vcam1tm1Dmil/Vcam1+
(involves: 129S4/SvJae * C57BL/6)
|
decreased cell chemotaxis
|
J:227109
|
Icam1tm1Jcgr/Icam1tm1Jcgr Vcam1tm1Dmil/Vcam1tm1Dmil
(involves: 129S4/SvJae * C57BL/6)
|
decreased cell chemotaxis
|
J:227109
|
impaired macrophage chemotaxis
|
J:227109
|
Icmttm1Hzo/Icmttm1Hzo
(involves: 129S/SvEv)
|
increased forebrain apoptosis
|
J:77742
|
increased neural tube apoptosis
|
J:77742
|
Icmttm1Mbrg/Icmttm1Mbrg Tg(Mx1-cre)1Cgn/?
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
decreased cell proliferation
|
J:88170
|
Icostm1Mak/Icostm1Mak
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:66702
|
Id1tm1Zhu/Id1tm1Zhu
(involves: 129S1/Sv * C57BL/6J)
|
decreased lung endothelial cell proliferation
|
J:125521
|
increased lung endothelial cell apoptosis
|
J:125521
|
increased vascular endothelial cell apoptosis
|
J:125521
|
Id1tm1Zhu/Id1tm1Zhu
(involves: 129S1/Sv * C57BL/6)
|
abnormal osteoclast differentiation
|
J:155384
|
Id1tm1Zhu/Id1tm1Zhu Id3tm1Zhu/Id3tm1Zhu
(involves: 129S1/Sv * 129S4/SvJaeSor)
|
abnormal neuronal precursor proliferation
|
J:86480,
J:170418
|
premature neuronal precursor differentiation
|
J:86480
|
Id1tm3Bene/Id1tm3Bene Id2tm1Xdz/Id2tm1Xdz Id3tm1Zhu/Id3tm1Zhu Tg(Nes-cre)1Kln/0
(involves: 129S4/SvJaeSor * C57BL/6 * SJL)
|
abnormal cell cycle
|
J:185426
|
abnormal neuron differentiation
|
J:185426
|
abnormal neuronal precursor proliferation
|
J:185426
|
premature neuronal precursor differentiation
|
J:185426
|
Id2tm1Ago/Id2tm1Ago
(B6.129-Id2tm1Ago)
|
abnormal cell differentiation
|
J:138276
|
Id2tm1Mcha/Id2tm1Mcha
(involves: C57BL/6 * CD-1)
|
abnormal neuronal precursor proliferation
|
J:143882
|
premature neuronal precursor differentiation
|
J:143882
|
Id3tm1Zhu/Id3tm1Zhu
(involves: 129/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:56950
|
Id4tm1Fsky/Id4tm1Fsky
(involves: 129P2/OlaHsd * CD-1)
|
abnormal neuron differentiation
|
J:98270
|
premature neuronal precursor differentiation
|
J:98270
|
Id4tm1Mais/Id4tm1Mais
(involves: 129X1/SvJ)
|
abnormal neuron differentiation
|
J:93574
|
Idd4C57BL/6/Idd4C57BL/6
(involves: C57BL/6 * DBA/2)
|
increased T cell proliferation
|
J:25969
|
Idd4C57BL/6/Idd4C57BL/6
(involves: C57BL/6 * NOD)
|
increased T cell proliferation
|
J:25969
|
Idd6C57BL/6/Idd6C57BL/6
(NOD.B6-Idd6C57BL/6/Umea)
|
abnormal apoptosis
|
J:84296
|
Idd6C57BL/6/Idd6NOD
(involves: C57BL/6 * NOD)
|
decreased apoptosis
|
J:84296
|
decreased T cell proliferation
|
J:72360
|
Idd6NOD/Idd6NOD
(involves: C57BL/6 * NOD)
|
decreased apoptosis
|
J:84296
|
decreased T cell proliferation
|
J:72360
|
Idetm1a(EUCOMM)Wtsi/Idetm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:274952
|
increased testis apoptosis
|
J:274952
|
necrospermia
|
J:274952
|
oxidative stress
|
J:274952
|
teratozoospermia
|
J:274952
|
Idh2tm1Jwpk/Idh2tm1Jwpk
(involves: 129S4/SvJae * C57BL/6)
|
oxidative stress
|
J:272241
|
Ido1tm1Alm/Ido1tm1Alm
(involves: 129X1/SvJ * BALB/c)
|
abnormal autophagy
|
J:170565
|
enlarged sperm head
|
J:170565
|
hairpin sperm flagellum
|
J:170565
|
pinhead sperm
|
J:170565
|
teratozoospermia
|
J:170565
|
Ido1tm1Alm/Ido1tm1Alm
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:282516
|
abnormal mitophagy
|
J:282516
|
abnormal oxidative phosphorylation
|
J:282516
|
decreased mitochondrial number
|
J:282516
|
Idstm1Dkji/Y
(involves: C57BL/6)
|
abnormal foam cell morphology
|
J:294717
|
abnormal lysosome physiology
|
J:294717
|
Idstm1Dkji/Y
(involves: 129 * C57BL/6)
|
abnormal lysosome physiology
|
J:294523
|
Idstm1Muen/Y
(Not Specified)
|
lysosomal protein accumulation
|
J:108761,
J:108242
|
Idstm1Muen/Y
(involves: C57BL/6)
|
abnormal lysosome physiology
|
J:259752
|
Iduatm1.1Kmke/Iduatm1.1Kmke
(B6.129-Iduatm1.1Kmke)
|
abnormal foam cell morphology
|
J:155619
|
abnormal lysosome morphology
|
J:155619
|
Iduatm1Clk/Iduatm1Clk
(involves: 129S1/Sv * 129X1/SvJ)
|
lysosomal protein accumulation
|
J:39522
|
Iduatm1Efn/Iduatm1Efn
(involves: C57BL/6)
|
abnormal lysosome morphology
|
J:123676
|
Ier3tm1Mxw/Ier3tm1Mxw
(involves: 129 * C57BL/6)
|
impaired macrophage phagocytosis
|
J:157504
|
Ier3ip1tm1Arvn/Ier3ip1tm1Arvn Tg(Ins1-cre/ERT)1Lphi/0
(involves: 129S4/SvJaeSor * C57BL/6J * CD-1)
|
abnormal pancreatic beta cell differentiation
|
J:336782
|
decreased pancreatic beta cell proliferation
|
J:336782
|
increased pancreatic beta cell apoptosis
|
J:336782
|
Ier3ip1tm1Arvn/Ier3ip1tm1Arvn Tg(Ins2-cre)25Mgn/0
(involves: C57BL/6 * C57BL/6J * DBA)
|
abnormal endoplasmic reticulum morphology
|
J:336782
|
abnormal endoplasmic reticulum physiology
|
J:336782
|
abnormal pancreatic beta cell differentiation
|
J:336782
|
decreased pancreatic beta cell proliferation
|
J:336782
|
increased endoplasmic reticulum stress
|
J:336782
|
increased pancreatic beta cell apoptosis
|
J:336782
|
Ifih1tm1Aki/Ifih1tm1Aki
(involves: 129/Sv * C57BL/6)
|
abnormal cell physiology
|
J:137522
|
Ifitm5em1Pmof/Ifitm5+
(involves: CD-1)
|
abnormal osteoblast physiology
|
J:255349
|
impaired osteoblast differentiation
|
J:255349
|
Ifnar1tm1Agt/Ifnar1tm1Agt
(involves: 129S2/SvPas * BALB/c)
|
decreased T cell apoptosis
|
J:291874
|
Ifnar1tm1Agt/Ifnar1tm1Agt Myd88tm1Aki/Myd88tm1Aki
(involves: 129P2/OlaHsd * 129S2/SvPas)
|
abnormal leukocyte migration
|
J:171379
|
Ifnb1tm1Acgp/Ifnb1tm1Acgp
(involves: 129P2/OlaHsd)
|
increased T cell proliferation
|
J:86527
|
Ifngtm1Ts/Ifngtm1Ts
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased splenocyte proliferation
|
J:66802
|
Ifngtm1Ts/Ifngtm1Ts
(NOD.129S7(B6)-Ifngtm1Ts/DvsJ)
|
abnormal diapedesis
|
J:72818
|
Ifngtm1Ts/Ifngtm1Ts
(B6.129S7-Ifngtm1Ts/J)
|
abnormal dendritic cell chemotaxis
|
J:134949
|
abnormal macrophage chemotaxis
|
J:136628
|
abnormal redox activity
|
J:122801
|
Ifngtm1Yiw/Ifngtm1Yiw
(involves: 129X1/SvJ * C57BL/6)
|
decreased apoptosis
|
J:41632
|
Ifngr1tm1Agt/Ifngr1tm1Agt
(involves: 129S7/SvEvBrd)
|
increased hepatocyte proliferation
|
J:38363
|
Ifngr1tm1Agt/Ifngr1tm1Agt
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased splenocyte proliferation
|
J:99347
|
Ifngr1tm1Agt/Ifngr1tm1Agt
(B6.129S7-Ifngr1tm1Agt/J)
|
abnormal osteoclast differentiation
|
J:233116
|
impaired osteoblast differentiation
|
J:233116
|
Ifngr1tm1Agt/Ifngr1tm1Agt Tg(GZMB-Tax)#Lera/0
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:147601
|
Ifngr2tm1Pbro/Ifngr2tm1Pbro
(NOD.129S1-Ifngr2tm1Pbro)
|
abnormal diapedesis
|
J:72818
|
Ifrd1tm1Lah/Ifrd1tm1Lah
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal white fat cell differentation
|
J:344868
|
Ifrd1tm1Lah/Ifrd1tm1Lah Ifrd2tm1.1Lah/Ifrd2tm1.1Lah
(involves: 129 * 129P2/OlaHsd * C57BL/6J)
|
abnormal white fat cell differentation
|
J:344868
|
Ifrd2tm1.1Lah/Ifrd2tm1.1Lah
(B6.129-Ifrd2tm1.1Lah)
|
abnormal white fat cell differentation
|
J:344868
|
Ift20tm1.1Gjp/Ift20tm1.1Gjp Tg(Hoxb7-cre)13Amc/0
(involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6)
|
absent kidney epithelial cell primary cilium
|
J:141071
|
increased kidney cell proliferation
|
J:141071
|
Ift20tm1.1Gjp/Ift20tm1.2Gjp Tg(Stra8-icre)1Reb/0
(involves: 129S4/SvJaeSor * 129S7/SvEvBrd * FVB/NJ)
|
abnormal outer dense fiber morphology
|
J:265626
|
abnormal sperm axoneme morphology
|
J:265626
|
abnormal sperm flagellum morphology
|
J:265626
|
abnormal sperm motility
|
J:265626
|
asthenozoospermia
|
J:265626
|
globozoospermia
|
J:265626
|
immotile sperm
|
J:265626
|
kinked sperm flagellum
|
J:265626
|
oligozoospermia
|
J:265626
|
short sperm flagellum
|
J:265626
|
teratozoospermia
|
J:265626
|
Ift27tm1a(EUCOMM)Hmgu/Ift27tm1a(EUCOMM)Hmgu
(involves: C57BL/6N)
|
abnormal keratinocyte differentiation
|
J:224085
|
cellular phenotype
|
J:224085
|
decreased keratinocyte proliferation
|
J:224085
|
Ift27tm1c(EUCOMM)Hmgu/Ift27tm1c(EUCOMM)Hmgu Tg(Stra8-icre)1Reb/0
(involves: 129S4/SvJae * C57BL/6J * C57BL/6N * FVB/NJ)
|
abnormal outer dense fiber morphology
|
J:251964
|
abnormal plasma membrane morphology
|
J:251964
|
abnormal sperm axoneme morphology
|
J:251964
|
abnormal sperm end piece morphology
|
J:251964
|
abnormal sperm fibrous sheath morphology
|
J:251964
|
abnormal sperm flagellum morphology
|
J:251964
|
abnormal sperm flagellum thickness
|
J:251964
|
abnormal sperm head morphology
|
J:251964
|
asthenozoospermia
|
J:251964
|
decreased sperm progressive motility
|
J:251964
|
disorganized sperm mitochondrial sheath
|
J:251964
|
globozoospermia
|
J:251964
|
immotile sperm
|
J:251964
|
kinked sperm flagellum
|
J:251964
|
oligozoospermia
|
J:251964
|
short sperm flagellum
|
J:251964
|
teratozoospermia
|
J:251964
|
Ift46tm1Cnu/Ift46tm1Cnu
(involves: C57BL/6)
|
absent embryonic cilia
|
J:221138
|
absent nodal flow
|
J:221138
|
Ift56hop-hpy/Ift56hop-hpy
(Not Specified)
|
teratozoospermia
|
J:14943,
J:5829
|
Ift56hop-hpy/Ift56hop-hpy Oca2p-s/Oca2p-s
(Not Specified)
|
teratozoospermia
|
J:89544
|
Ift56hop/Ift56hop
(Not Specified)
|
abnormal male meiosis
|
J:5206
|
abnormal manchette morphology
|
J:89468
|
abnormal sperm flagellum morphology
|
J:5206
|
abnormal spermatid morphology
|
J:5206
|
absent sperm flagellum
|
J:5206
|
azoospermia
|
J:5206,
J:89468
|
Ift56hop/Ift56hop
(CByJ.Cg-Ift56hop/J)
|
abnormal motile primary cilium morphology
|
J:216284
|
Ift57tm1Dwni/Ift57tm1Dwni
(involves: 129S1/SvImJ * C57BL/6J)
|
absent embryonic cilia
|
J:119664
|
Ift57tm2Dwni/Ift57tm2Dwni
(involves: 129S1/SvImJ * C57BL/6J)
|
absent embryonic cilia
|
J:119664
|
Ift74tm1c(EUCOMM)Hmgu/Ift74tm1c(EUCOMM)Hmgu Tg(Stra8-icre)1Reb/0
(involves: 129S4/SvJaeSor * C57BL/6N * FVB/NJ)
|
abnormal sperm axoneme morphology
|
J:277145
|
abnormal sperm head morphology
|
J:277145
|
abnormal spermatid morphology
|
J:277145
|
absent sperm axonemal central pair
|
J:277145
|
absent sperm flagellum
|
J:277145
|
asthenozoospermia
|
J:277145
|
immotile sperm
|
J:277145
|
oligozoospermia
|
J:277145
|
short sperm flagellum
|
J:277145
|
teratozoospermia
|
J:277145
|
Ift80tm1c(KOMP)Wtsi/Ift80tm1c(KOMP)Wtsi Tg(Npy2r-cre)1Tfur/0
(involves: C3H * C57BL/6JJcl * C57BL/6N)
|
abnormal motile cilium morphology
|
J:226948
|
Ift81tm1c(EUCOMM)Wtsi/Ift81tm1c(EUCOMM)Wtsi Tg(Stra8-icre)1Reb/0
(involves: C57BL/6 * C57BL/6N * FVB/NJ)
|
abnormal acrosome morphology
|
J:292151
|
abnormal sperm axoneme morphology
|
J:292151
|
abnormal sperm fibrous sheath morphology
|
J:292151
|
abnormal sperm flagellum morphology
|
J:292151
|
abnormal sperm head morphology
|
J:292151
|
abnormal sperm midpiece morphology
|
J:292151
|
abnormal sperm nucleus morphology
|
J:292151
|
asthenozoospermia
|
J:292151
|
disorganized sperm mitochondrial sheath
|
J:292151
|
immotile sperm
|
J:292151
|
kinked sperm flagellum
|
J:292151
|
multinucleated giant male germ cells
|
J:292151
|
oligozoospermia
|
J:292151
|
short sperm flagellum
|
J:292151
|
Ift88Tg737Rpw/Ift88Tg737Rpw
(involves: FVB/N)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:65500
|
decreased pancreatic primary cilium length
|
J:90990
|
decreased pancreatic primary cilium number
|
J:90990
|
Ift88Tg737Rpw/Ift88Tg737Rpw
(FVB/N-Ift88Tg737Rpw)
|
decreased pancreatic primary cilium length
|
J:95813
|
decreased pancreatic primary cilium number
|
J:95813
|
Ift88tm1.1Bky/Ift88tm1.1Bky
(involves: 129P2/OlaHsd)
|
absent embryonic cilia
|
J:297055
|
Ift88tm1Bky/Ift88tm1Bky Nfatc1tm1.1(cre)Bz/Nfatc1+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
abnormal motile cilium morphology
|
J:291454
|
Ift88tm1Rpw/Ift88tm1Rpw
(FVB.129-Ift88tm1Rpw)
|
absent embryonic cilia
|
J:62025
|
Ift122sopb/Ift122sopb
(C3Fe.B6-Ift122sopb)
|
abnormal cilium morphology
|
J:168317
|
abnormal motile primary cilium morphology
|
J:168317
|
Ift122sopb/Ift122sopb Kif3atm1Gsn/Kif3atm1Gsn
(involves: 129S1/Sv * 129X1/SvJ * C3HeB/FeJ * C57BL/6J)
|
absent embryonic cilia
|
J:168317
|
Ift140cauli/Ift140cauli
(involves: C3H/HeH * C57BL/6JAnu)
|
abnormal primary cilium morphology
|
J:220659
|
Ift140tm1b(KOMP)Wtsi/Ift140tm1c(KOMP)Wtsi Tg(Hoxb7-cre)13Amc/?
(B6J.B6-Ift140tm1b(KOMP)Wtsi/Ift140tm1c(Komp)Wtsi Tg(Hoxb7-cre)13Amc)
|
cellular phenotype
|
J:181533
|
decreased kidney epithelial cell primary cilium length
|
J:181533
|
increased kidney apoptosis
|
J:181533
|
increased kidney cell proliferation
|
J:181533
|
Ift140tm1c(KOMP)Wtsi/Ift140tm1c(KOMP)Wtsi Tg(Stra8-icre)1Reb/0
(involves: C57BL/6N * FVB/NJ)
|
abnormal manchette morphology
|
J:285527
|
abnormal outer dense fiber morphology
|
J:285527
|
abnormal sperm axoneme morphology
|
J:285527
|
abnormal sperm end piece morphology
|
J:285527
|
abnormal sperm fibrous sheath morphology
|
J:285527
|
abnormal sperm flagellum morphology
|
J:285527
|
abnormal sperm head morphology
|
J:285527
|
abnormal sperm mitochondrial morphology
|
J:285527
|
abnormal sperm nucleus morphology
|
J:285527
|
abnormal spermatid morphology
|
J:285527
|
asthenozoospermia
|
J:285527
|
decreased sperm progressive motility
|
J:285527
|
immotile sperm
|
J:285527
|
kinked sperm flagellum
|
J:285527
|
oligozoospermia
|
J:285527
|
short sperm flagellum
|
J:285527
|
teratozoospermia
|
J:285527
|
Ift172avc1/Ift172avc1
(involves: C57BL/6J)
|
abnormal cilium morphology
|
J:175371
|
abnormal motile primary cilium morphology
|
J:175371
|
Ift172avc1/Ift172wim
(involves: C57BL/6J)
|
abnormal cilium morphology
|
J:175371
|
abnormal motile primary cilium morphology
|
J:175371
|
Ift172tm1.1Rama/Ift172tm1.1Rama Tg(Stra8-icre)1Reb/0
(involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ)
|
abnormal acrosome morphology
|
J:302808
|
abnormal centrosome morphology
|
J:302808
|
abnormal outer dense fiber morphology
|
J:302808
|
abnormal sperm axoneme morphology
|
J:302808
|
abnormal sperm flagellum morphology
|
J:302808
|
abnormal sperm head morphology
|
J:302808
|
abnormal sperm midpiece morphology
|
J:302808
|
abnormal spermatid morphology
|
J:302808
|
asthenozoospermia
|
J:302808
|
ectopic manchette
|
J:302808
|
elongated manchette
|
J:302808
|
kinked sperm flagellum
|
J:302808
|
oligozoospermia
|
J:302808
|
teratozoospermia
|
J:302808
|
Ift172wim/Ift172wim
(C3.B6J-Ift172wim)
|
absent embryonic cilia
|
J:86437
|
Ift172wim/Ift172wim
(involves: C57BL/6J)
|
abnormal cilium morphology
|
J:138139
|
Iftaptm1b(KOMP)Wtsi/Iftaptm1b(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal sperm head morphology
|
J:268060
|
Igdmrtm1Ace/Igdmr+
(involves: 129P2/OlaHsd * C57BL/6)
|
paternal imprinting
|
J:91849
|
Igf1tm1Arge/Igf1tm1Arge
(involves: 129S/SvEv * MF1)
|
increased neuron apoptosis
|
J:71687
|
Igf1tm1Arge/Igf1tm1Arge Igf2tm1Rob/Igf2+
(either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J) or (involves: 129S/SvEv * MF1))
|
maternal imprinting
|
J:15108
|
Igf1rtm1.1Mhz/Igf1rtm1.1Mhz Insrtm1Khn/Insrtm1Khn Tg(Ckmm-cre)5Khn/0
(involves: 129/Sv * 129S4/SvJae * C57BL/6 * FVB)
|
cardiac interstitial fibrosis
|
J:118987
|
Igf1rtm1Arge/Igf1rtm1Arge
(involves: 129S/SvEv)
|
decreased oligodendrocyte progenitor number
|
J:15108
|
Igf1rtm1Arge/Igf1rtm1Arge Igf2tm1Rob/Igf2+
(involves: 129S/SvEv)
|
maternal imprinting
|
J:15108
|
Igf1rtm1Arge/Igf1rtm2Arge Tg(Camk2a-cre)2Szi/0
(involves: 129S/SvEv * C57BL/6J * CBA)
|
decreased oligodendrocyte progenitor number
|
J:88198
|
Igf1rtm1Jcbr/Igf1rtm1Jcbr Ndor1Tg(UBC-cre/ERT2)1Ejb/0
(involves: 129S/SvEv * C57BL/6)
|
azoospermia
|
J:221618
|
increased hepatocyte proliferation
|
J:221618
|
oligozoospermia
|
J:221618
|
Igf1rtm2.1Arge/Igf1rtm2.1Arge
(involves: 129 * C57BL/6)
|
abnormal inner hair cell kinocilium morphology
|
J:178908
|
Igf1rtm2Arge/Igf1rtm2Arge Tg(BGLAP-cre)1Clem/0
(involves: 129 * FVB/N)
|
abnormal osteoblast physiology
|
J:80190
|
Igf2tm1Rob/Igf2+
(involves: 129S/SvEv * MF1)
|
maternal imprinting
|
J:11007
|
Igf2tm1Rob/Igf2+
(involves: 129S/SvEv * BALB/c)
|
maternal imprinting
|
J:11007
|
Igf2tm1Rob/Igf2+
(involves: 129S/SvEv * C57BL/6 * DBA/2J)
|
maternal imprinting
|
J:11007
|
Igf2tm1Rob/Igf2+
(involves: 129S/SvEv)
|
maternal imprinting
|
J:15108,
J:11007
|
Igf2tm1Rob/Igf2+
(involves: 129S/SvEv * C57BL/6J)
|
abnormal fetal cardiomyocyte proliferation
|
J:77413
|
increased hepatocyte proliferation
|
J:77413
|
Igf2tm1Rob/Igf2tm4.1Wrk
(involves: 129P2/OlaHsd * 129S/SvEv * BALB/c * C57BL/6)
|
abnormal imprinting
|
J:178292
|
Igf2tm1Snha/Igf2+
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
abnormal osteoblast differentiation
|
J:167738
|
abnormal osteoclast differentiation
|
J:167738
|
maternal imprinting
|
J:167738
|
Igf2tm1Wrk/Igf2+
(involves: 129P2/Ola * C57BL/6J)
|
maternal imprinting
|
J:65001,
J:90697
|
Igf2tm2Wrk/Igf2+
(involves: 129S1/Sv * C57BL/6)
|
maternal imprinting
|
J:94521
|
Igf2tm3Wrk/Igf2+
(Not Specified)
|
maternal imprinting
|
J:94521
|
Igf2tm4.1Wrk/Igf2+
(involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SD7)
|
abnormal imprinting
|
J:178292
|
Igf2tm4Wrk/Igf2+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal imprinting
|
J:169366
|
Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal colon goblet cell morphology
|
J:89882
|
decreased cell proliferation
|
J:89882
|
Igf2bp1Gt(OST33739)Lex/Igf2bp1Gt(OST33739)Lex
(involves: 129S5/SvEvBrd)
|
abnormal cell cycle
|
J:207231
|
decreased cell proliferation
|
J:207231
|
premature neuronal precursor differentiation
|
J:207231
|
Igf2bp1Gt(XL009)Byg/Igf2bp1Gt(XL009)Byg
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:187686
|
Igf2rtm1.1Rlj/Igf2r+
(involves: 129/Sv * BALB/cJ * C57BL/6J)
|
genetic imprinting
|
J:80932
|
Igf2rtm1Rlj/Igf2r+ Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129/Sv * C57BL/6 * DBA)
|
genetic imprinting
|
J:80932
|
Igf2rtm1Rlj/Igf2r+ Tg(Ckmm-cre)1Lrsn/0
(involves: 129 * C57BL/6J)
|
genetic imprinting
|
J:80932
|
Igf2rtm1Wag/Igf2r+
(involves: 129S2/SvPas)
|
abnormal lysosome physiology
|
J:20763
|
maternal imprinting
|
J:20763
|
Igf2rtm1Wag/Igf2rtm1Wag
(involves: 129S2/SvPas)
|
abnormal lysosome physiology
|
J:20763
|
Igfbp1tm1Taub/Igfbp1tm1Taub
(involves: 129X1/SvJ * C57BL/6)
|
increased hepatocyte apoptosis
|
J:81123
|
Igfbp3tm1Jep/Igfbp3tm1Jep
(involves: 129S/SvEv * C57BL/6J)
|
oxidative stress
|
J:282246
|
Igfbp7tm1.1Dds/Igfbp7tm1.1Dds
(involves: CD-1)
|
decreased fibroblast proliferation
|
J:212964
|
decreased mammary gland epithelial cell proliferation
|
J:212964
|
Igh-7tm1Gach/Igh-7tm1Gach
(BALB/c-Igh-7tm1Gach)
|
enhanced B cell migration
|
J:143266
|
Igh-Jtm1Dhu/Igh-J+ Il2tm1Hor/Il2tm1Hor
(involves: 129/Sv * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:29999
|
Igh-Jtm1Dhu/Igh-Jtm1Dhu Il2tm1Hor/Il2tm1Hor
(involves: 129/Sv * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:29999
|
Igh-Vtm1(Igh-Vx24)Hmb/Igh-Vtm1(Igh-Vx24)Hmb
(involves: 129/Sv * C57BL/6)
|
increased apoptosis
|
J:54380
|
increased cell proliferation
|
J:54380
|
Ightm1(Myc)Janz/Igh+
(involves: 129X1/SvJ * C57BL/6)
|
increased B cell apoptosis
|
J:96785
|
increased B cell proliferation
|
J:96785
|
Ightm1(Myc)Janz/Igh+ Mdm4tm1.1Wahl/Mdm4tm1.1Wahl
(involves: 129S/Sv * C57BL/6)
|
increased splenocyte proliferation
|
J:150341
|
Ightm1.1(Igh564)Tik/Ightm1.1(Igh564)Tik Igktm1(Igk564)Tik/Igktm1(Igk564)Tik
(B6.129S4-Igktm1(Igk564)Tik Ightm1(Igh564)Tik)
|
increased mesangial cell number
|
J:113555
|
Ightm1.2Rsky/Ightm1.2Rsky
(BALB/c-Ightm1.2Rsky)
|
abnormal B cell proliferation
|
J:125719
|
Ightm1Mnz/Ightm1Mnz
(B6.129P2-Ightm1Mnz)
|
abnormal cell cycle
|
J:75653
|
increased B cell apoptosis
|
J:75653
|
increased B cell proliferation
|
J:75653
|
Ightm1Mnz/Ightm1Mnz Lyntm1Sor/Lyntm1Sor
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6)
|
increased B cell proliferation
|
J:75653
|
Ightm2Cgn/Igh+ Rr158tm1Cgn/Rr158tm1Cgn Arhgef1tm1.1Rmt/Arhgef1tm1.1Rmt
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal B cell migration
|
J:113295
|
Ightm2Cgn/Ightm2Cgn Igktm1Rsky/Igktm1Rsky Trp53tm1Tyj/Trp53tm1Tyj Xrcc4tm1Fwa/Xrcc4tm1Fwa
(involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac)
|
increased cellular sensitivity to ionizing radiation
|
J:126758
|
spontaneous chromosome breakage
|
J:126758
|
Ightm2Mnz/Ightm2Mnz
(B6.129P2-Ightm2Mnz)
|
cellular phenotype
|
J:75653
|
increased B cell proliferation
|
J:75653
|
Ightm2Mnz/Ightm2Mnz Lyntm1Sor/Lyntm1Sor
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6)
|
increased B cell proliferation
|
J:75653
|
Ightm3(IGH)Vlcg/Ightm3(IGH)Vlcg
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
impaired sperm migration in female genital tract
|
J:277644
|
Ighatm1(Myc)Janz/Igha+
(involves: 129S1/Sv * C57BL/6)
|
increased B cell apoptosis
|
J:90901
|
increased B cell proliferation
|
J:90901
|
Ighatm1(Myc)Janz/Igha+ Tg(Igk-V21-Bax)1967Bvn/0
(involves: 129S1/Sv * C57BL/6 * FVB/N)
|
abnormal B cell apoptosis
|
J:90901
|
Ighatm1Grh/Ighatm1Grh
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased T cell proliferation
|
J:125472
|
Ighg2cem2Wliu/Ighg2cem2Wliu
(C57BL/6J-Ighg2cem2Wliu)
|
impaired macrophage phagocytosis
|
J:322180
|
Ighmtm1(Bcl6)Rdf/?
(involves: 129/Sv * C57BL/6)
|
abnormal B cell proliferation
|
J:98937
|
Ighmtm1.1(IGH-2)Cog/Ighmtm1.1(IGH-2)Cog
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
decreased B cell proliferation
|
J:157575
|
increased B cell proliferation
|
J:157575
|
Ighmtm1Cgn/Ighm+ Tgfb1tm1Doe/Tgfb1tm1Doe
(involves: 129S2/SvPas * C57BL/6 * CF-1)
|
increased cell proliferation
|
J:99033
|
Ighmtm1Cgn/Ighmtm1Cgn
(involves: 129S2/SvPas)
|
decreased T cell proliferation
|
J:112160
|
Ighmtm1Cgn/Ighmtm1Cgn
(NOD.129S2-Ighmtm1Cgn/DvsJ)
|
abnormal T cell proliferation
|
J:80859
|
Ighmtm1Cgn/Ighmtm1Cgn Tg(IghelMD4)4Ccg/Tg(IghelMD4)4Ccg
(NOD.Cg-Ighmtm1Cgn Tg(IghelMD4)4Ccg/DvsJ)
|
abnormal T cell proliferation
|
J:80859
|
Ighmtm3Bgmn/Ighmtm3Bgmn
(involves: 129)
|
decreased B cell proliferation
|
J:131633
|
Ighmtm4Bgmn/Ighmtm4Bgmn
(involves: 129)
|
decreased B cell proliferation
|
J:131633
|
Ighmbp2nmd-2J/Ighmbp2nmd-2J
(B6.BKS-Ighmbp2nmd-2J/J)
|
abnormal cell cytoskeleton morphology
|
J:92862
|
cardiac interstitial fibrosis
|
J:90418
|
Igs2em5(CAG-Mir802)Gpt/Igs2em5(CAG-Mir802)Gpt Tg(Ins2-cre)25Mgn/0
(involves: C57BL/6JGpt * DBA)
|
abnormal pancreatic beta cell differentiation
|
J:287584
|
Igs2tm1(CAG-mt-Keima)Fink/Igs2+ Kansl1em1.1Cya/Kansl1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N)
|
abnormal mitophagy
|
J:327464
|
Igs2tm1(CAG-mt-Keima)Fink/Igs2+ Lamp2tm1Psa/Lamp2tm1Psa
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
abnormal mitophagy
|
J:253728
|
Igsf3em1Laap/Igsf3em1Laap
(FVB/NRj-Igsf3em1Laap)
|
abnormal vagal neural crest cell migration
|
J:341537
|
Ihhtm1Amc/Ihhtm1Amc
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased chondrocyte proliferation
|
J:73071
|
Iho1tm1.2Atot/Iho1tm1.2Atot
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal spermatocyte morphology
|
J:276412
|
Iigp1cem1Btlr/Iigp1cem1Btlr
(C57BL/6J-Iigp1cem1Btlr)
|
abnormal lipid oxidation
|
J:333470
|
Ikbkbtm1.1Cgn/Ikbkbtm1.1Cgn
(involves: C57BL/6)
|
increased fibroblast apoptosis
|
J:85810
|
Ikbkbtm1Lex/Ikbkbtm1Lex Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S/SvEvBrd)
|
impaired macrophage chemotaxis
|
J:159873
|
impaired neutrophil chemotaxis
|
J:159873
|
Ikbkbtm1Trk/Ikbkbtm1Trk
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell physiology
|
J:55680
|
increased fibroblast apoptosis
|
J:55680
|
increased hepatocyte apoptosis
|
J:55680
|
Ikbkbtm1Ver/Ikbkbtm1Ver
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell physiology
|
J:54323
|
increased fibroblast apoptosis
|
J:54323
|
increased hepatocyte apoptosis
|
J:54323
|
Ikbkbtm2Mka/Ikbkbtm2.1Mka Tg(Vil-cre)1Mka/0
(involves: 129)
|
increased cellular sensitivity to gamma-irradiation
|
J:88644
|
increased enterocyte apoptosis
|
J:88644
|
Ikbkbtm2Mka/Ikbkbtm2Mka Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129/Sv * 129P2/OlaHsd)
|
increased macrophage apoptosis
|
J:80159
|
Ikbketm1Tman/Ikbketm1Tman
(B6.Cg-Ikbketm1Tman)
|
abnormal fibroblast physiology
|
J:119791
|
Ikbkgm1Btlr/Y
(C57BL/6J-Ikbkgm1Btlr)
|
azoospermia
|
J:139558
|
Ikbkgtm1.1Chtr/Y Tg(Alb1-cre)7Gsc/0
(involves: C57BL/6 * FVB/N * SJL)
|
increased hepatocyte apoptosis
|
J:151485
|
Ikbkgtm1.1Chtr/Ikbkgtm1.1Chtr Map3k7tm1Aki/Map3k7tm1Aki Tg(Alb1-cre)7Gsc/0
(involves: 129P2/OlaHsd * FVB/N)
|
increased hepatocyte apoptosis
|
J:160521
|
increased hepatocyte proliferation
|
J:160521
|
Ikbkgtm1.1Chtr/Ikbkgtm1.1Chtr Tg(Alb1-cre)7Gsc/0
(involves: C57BL/6 * FVB/N * SJL)
|
increased hepatocyte apoptosis
|
J:151485
|
Ikbkgtm1.1Chtr/Ikbkgtm1.1Chtr Tg(Alb1-cre)7Gsc/0
(involves: FVB/N)
|
increased hepatocyte apoptosis
|
J:160521
|
increased hepatocyte proliferation
|
J:160521
|
Ikbkgtm1.1Mpa/Y Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * DBA/2)
|
increased T cell apoptosis
|
J:85810
|
Ikbkgtm1.1Mpa/Ikbkgtm1.1Mpa Tg(Alb1-cre)7Gsc/0
(involves: C57BL/6 * FVB/N)
|
abnormal hepatocyte mitochondrial morphology
|
J:118336
|
increased apoptosis
|
J:118336
|
increased cell proliferation
|
J:118336
|
Ikbkgtm1Mak/Y
(involves: 129P2/OlaHsd * C57BL/6)
|
increased fibroblast apoptosis
|
J:61666
|
increased hepatocyte apoptosis
|
J:61666
|
Ikbkgtm1Mka/Y
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
increased hepatocyte apoptosis
|
J:63054
|
Ikbkgtm1Mka/Ikbkg+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
increased apoptosis
|
J:63054
|
increased hepatocyte apoptosis
|
J:63054
|
increased keratinocyte apoptosis
|
J:63054
|
Ikbkgtm1Mpa/Y
(involves: C57BL/6)
|
increased fibroblast apoptosis
|
J:63055
|
Ikbkgtm1Mpa/Ikbkg+
(involves: C57BL/6)
|
increased keratinocyte apoptosis
|
J:63055
|
Ikzf1plstc/Ikzf1plstc
(C57BL/6JSfdAnu-Ikzf1plstc)
|
abnormal granulocyte differentiation
|
J:84569
|
abnormal macrophage differentiation
|
J:84569
|
Ikzf1tm1Kast/Ikzf1tm1Kast
(involves: 129S2/SvPas)
|
decreased B cell proliferation
|
J:82813
|
Ikzf1tm1Kge/Ikzf1+
(involves: 129S4/SvJae * C57BL/6)
|
increased T cell proliferation
|
J:29355
|
Ikzf1tm1Kge/Ikzf1+
(involves: 129S4/SvJae * BALB/c)
|
increased T cell proliferation
|
J:29355
|
Ikzf1tm2Kge/Ikzf1tm2Kge
(involves: 129S4/SvJae)
|
increased T cell proliferation
|
J:37317
|
Ikzf1tm3Kge/Ikzf1tm3Kge Tg(CD2-icre)4Kio/?
(involves: C57BL/10 * CBA/Ca)
|
impaired B cell migration
|
J:209927
|
Ikzf1tm3Kge/Ikzf1tm3Kge Tg(CD19-cre/ERT2)1Cgn/?
(Not Specified)
|
abnormal B cell apoptosis
|
J:209927
|
Ikzf3tm1Kge/Ikzf3tm1Kge
(involves: 129S4/SvJae * C57BL/6)
|
increased B cell proliferation
|
J:50626
|
increased T cell proliferation
|
J:50626
|
Ikzf4tm1.1Etms/Ikzf4tm1.1Etms
(Not Specified)
|
decreased T cell proliferation
|
J:295208
|
Il1r1tm1Roml/Il1r1tm1Roml
(NOD.Cg-Il1r1tm1Roml)
|
abnormal cell death
|
J:87251
|
Il1r1tm1Roml/Il1r1tm1Roml
(C.Cg-Il1r1tm1Roml)
|
decreased T cell proliferation
|
J:82863
|
Il1r1tm1Roml/Il1r1tm1Roml
(involves: 129S1/Sv * BALB/c)
|
impaired neutrophil chemotaxis
|
J:124226
|
Il1rntm1.1Cga/Il1rntm1.1Cga Lyz2tm1(cre)Ifo/Lyz2+
(D1.Cg-Il1rntm1.1Cga Lyz2tm1(cre)Ifo)
|
increased T cell proliferation
|
J:162760
|
Il1rntm1Sush/Il1rntm1Sush
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal dendritic cell differentiation
|
J:97684
|
Il2tm1.1Kasm/Il2tm1.1Kasm Ndor1Tg(UBC-cre/ERT2)1Ejb/?
(involves: 129S/SvEv * C57BL/6)
|
abnormal cellular respiration
|
J:190168
|
Il2tm1Hor/Il2tm1Hor
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal colon goblet cell morphology
|
J:29999,
J:15223
|
decreased splenocyte proliferation
|
J:79241
|
decreased T cell proliferation
|
J:39989,
J:26198
|
increased B cell proliferation
|
J:16662
|
increased T cell proliferation
|
J:15223,
J:16662
|
Il2tm1Hor/Il2tm1Hor
(C.129P2-Il2tm1Hor)
|
increased B cell proliferation
|
J:29799
|
increased T cell proliferation
|
J:29799
|
Il2tm1Hor/Il2tm1Hor
(B6.129P2-Il2tm1Hor)
|
increased T cell proliferation
|
J:28924
|
Il2tm1Hor/Il2tm1Hor
(B6.129P2-Il2tm1Hor/J)
|
abnormal cellular respiration
|
J:190168
|
abnormal T cell proliferation
|
J:190168
|
Il2tm1Hor/Il2tm1Hor Il4tm1Cgn/Il4tm1Cgn
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:16662
|
increased T cell proliferation
|
J:16662
|
Il2tm1Hor/Il2tm1Hor Rag2tm1Fwa/Rag2+
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:29999
|
Il2tm1Hor/Il2tm1Hor Tg(DO11.10)10Dlo/?
(C.Cg-Il2tm1Hor Tg(DO11.10)10Dlo)
|
increased T cell proliferation
|
J:88349
|
Il2rbtm1Mak/Il2rbtm1Mak
(B6.129-Il2rbtm1Mak)
|
decreased T cell proliferation
|
J:113547
|
Il2rbtm1Mak/Il2rbtm1Mak
(C.129-Il2rbtm1Mak)
|
decreased T cell proliferation
|
J:113547
|
Il2rgtm1Cgn/Y
(involves: 129 * CB20)
|
decreased T cell proliferation
|
J:22521
|
Il2rgtm1Cgn/Il2rgtm1Cgn
(involves: 129 * CB20)
|
decreased T cell proliferation
|
J:22521
|
Il2rgtm1Wjl/Y
(involves: 129S4/SvJae * C57BL/6)
|
decreased T cell proliferation
|
J:24117
|
Il2rgtm1Wjl/Y Prkdcscid/Prkdcscid
(NOD.Cg-Prkdcscid Il2rgtm1Wjl/Sz)
|
increased cellular sensitivity to X-ray irradiation
|
J:109833
|
Il2rgtm1Wjl/Il2rgtm1Wjl Prkdcscid/Prkdcscid
(NOD.Cg-Prkdcscid Il2rgtm1Wjl/Sz)
|
increased cellular sensitivity to X-ray irradiation
|
J:109833
|
Il3tm1Glli/Il3tm1Glli
(either: (involves: 129S2/SvPas * BALB/c) or (involves: 129S2/SvPas * C57BL/6))
|
abnormal mast cell differentiation
|
J:80500
|
Il4/Il13tm3Anjm/Il4/Il13tm3Anjm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:113543
|
Il4/Il13tm3Anjm/Il4/Il13tm3Anjm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:113543
|
Il4tm1(CD2)Irvr/Il4+
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:111440
|
Il4tm1Lky/Il4tm1Lky Itktm1Litt/Itktm1Litt
(involves: 129S4/SvJae * BALB/c * C57BL/6J)
|
abnormal cell death
|
J:129883
|
Il4tm2Nnt/Il4tm2Nnt
(BALB/c-Il4tm2Nnt/J)
|
abnormal dendritic cell differentiation
|
J:141937
|
Il4ratm1Fbb/Il4ratm1Fbb
(involves: BALB/cJ)
|
impaired macrophage chemotaxis
|
J:114751
|
Il4ratm1Fbb/Il4ratm2Fbb Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * BALB/c)
|
abnormal intestinal goblet cell morphology
|
J:114751
|
Il4ratm1Tch/Il4ratm1Tch
(involves: 129X1/SvJ * BALB/c)
|
decreased T cell proliferation
|
J:86215
|
Il5tm1Anjm/Il5tm1Anjm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:113543
|
Il5tm1Anjm/Il5tm1Anjm Il9tm1Anjm/Il9tm1Anjm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:113543
|
Il5tm2Anjm/Il5tm2Anjm Il9tm1Anjm/Il9tm1Anjm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:113543
|
Il5ratm1Ktk/Il5ratm1Ktk
(B6.129P2-Il5ratm1Ktk)
|
decreased B cell proliferation
|
J:89849
|
Il6tm1Kopf/Il6+ Ncoa5tm1Hxia/Ncoa5+
(involves: 129 * 129S2/SvPas * C57BL/6)
|
increased sperm motility
|
J:284227
|
increased sperm progressive motility
|
J:284227
|
teratozoospermia
|
J:284227
|
Il6tm1Kopf/Il6tm1Kopf
(involves: 129S2/SvPas * C57BL/6)
|
abnormal myoblast migration
|
J:131016
|
abnormal skeletal muscle satellite cell proliferation
|
J:131016
|
Il6tm1Mur/Il6tm1Mur
(B6.129P2(B6)-Il6tm1Mur)
|
abnormal osteoblast differentiation
|
J:65093
|
abnormal osteoclast differentiation
|
J:65093
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:86039
|
Il6tm1Poli/Il6tm1Poli
(CAnNCrl.129S(Cg)-Il6tm1Poli)
|
abnormal B cell proliferation
|
J:42869
|
Il6ratm1.1Jcbr/Il6ratm1.1Jcbr Tg(Alb1-cre)7Gsc/0
(involves: C57BL/6 * FVB/N)
|
decreased adipocyte glucose uptake
|
J:166367
|
Il6ratm1.2Jcbr/Il6ratm1.2Jcbr
(involves: C57BL/6)
|
decreased hepatocyte proliferation
|
J:202764
|
increased hepatocyte apoptosis
|
J:202764
|
Il6sttm1Ard/Il6sttm1Ard
(involves: 129S1/Sv * C57BL/6)
|
increased cell proliferation
|
J:79555
|
Il6sttm1Kish/Il6sttm1Kish
(involves: 129P2/OlaHsd * CD-1)
|
abnormal osteoblast physiology
|
J:88710
|
abnormal osteoclast differentiation
|
J:88710
|
Il6sttm1Thir/Il6sttm1Thir
(B6.Cg-Il6sttm1Thir)
|
abnormal osteoblast physiology
|
J:144906
|
Il6sttm2Thir/Il6sttm2Thir
(B6.Cg-Il6sttm2Thir)
|
abnormal osteoblast physiology
|
J:144906
|
Il7rtm1Abra/Il7rtm1Abra
(B6.129S4-Il7rtm1Abra)
|
abnormal T cell proliferation
|
J:125360
|
Il7rtm1Imx/Il7rtm1Imx Tg(Lck-Il7r)1676Trma/?
(involves: 129S7/SvEvBrd * C57BL/6 * SJL)
|
decreased T cell proliferation
|
J:66400
|
increased thymocyte apoptosis
|
J:66400
|
Il9tm1Anjm/Il9tm1Anjm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:82881
|
Il10tm1Cgn/Il10tm1Cgn
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoblast differentiation
|
J:93577
|
decreased T cell proliferation
|
J:125760
|
increased hepatocyte apoptosis
|
J:110238
|
Il10tm1Cgn/Il10tm1Cgn
(B6.129P2-Il10tm1Cgn/J)
|
increased susceptibility to neuronal excitotoxicity
|
J:108086
|
Il10tm1Cgn/Il10tm1Cgn Vdrtm1Mbd/Vdrtm1Mbd
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
decreased T cell proliferation
|
J:107077
|
increased T cell apoptosis
|
J:107077
|
Il10ratm1.1Tlg/Il10ratm1.1Tlg Tg(Cd4-cre)1Cwi/?
(B6.Cg-Tg(Cd4-cre)1Cwi Il10ratm1.1Tlg)
|
decreased splenocyte proliferation
|
J:189797
|
Il10rbtm1Agt/Il10rbtm1Agt
(involves: 129S2/SvPas * C57BL/6)
|
abnormal granulocyte differentiation
|
J:45917
|
Il11tm1Moto/Il11tm1Moto
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal fat cell differentiation
|
J:345337
|
impaired osteoblast differentiation
|
J:345337
|
Il11ra1tm2Gos/Il11ra1tm2Gos
(involves: 129S2/SvPas * C57BL/6J)
|
maternal effect
|
J:48920
|
Il13tm1.1Anjm/Il13tm1.1Anjm
(C.129P2-Il13tm1.1Anjm)
|
abnormal dendritic cell differentiation
|
J:141937
|
Il13tm1Anjm/Il13tm1Anjm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:82881
|
Il13ra2tm1Gru/Il13ra2tm1Gru
(B6.Cg-Il13ra2tm1Gru)
|
increased lung apoptosis
|
J:236976
|
Il15ratm1.1Nsl/Il15ratm1.1Nsl
(involves: 129X1/SvJ * C57BL/6)
|
abnormal T cell apoptosis
|
J:73738
|
increased thymocyte apoptosis
|
J:73738
|
Il15ratm1.1Nsl/Il15ratm1.1Nsl
(B6.129X1-Il15ratm1.1Nsl)
|
abnormal T cell proliferation
|
J:92705
|
increased T cell proliferation
|
J:92705
|
Il15ratm1.1Nsl/Il15ratm1.1Nsl Tg(TcrAND)53Hed/?
(involves: 129X1/SvJ * C57BL/6 * SJL)
|
increased T cell proliferation
|
J:92705
|
Il15ratm1Ama/Il15ratm1Ama
(involves: 129X1/SvJ)
|
decreased T cell proliferation
|
J:142570
|
Il15ratm1Wjl/Il15ratm1Wjl
(involves: 129 * C57BL/6)
|
decreased T cell proliferation
|
J:142570
|
Il17a/Il17ftm1.1Impr/Il17a/Il17ftm1.1Impr
(involves: C57BL/6)
|
increased T cell proliferation
|
J:187400
|
Il17a/Il17ftm1.1Impr/Il17a/Il17ftm1.1Impr
(involves: C57BL/6)
|
increased T cell proliferation
|
J:187400
|
Il17ctm1Lex/Il17ctm1Lex
(B6.129S5-Il17ctm1Lex)
|
decreased keratinocyte proliferation
|
J:178967
|
Il17ratm1Koll/Il17ratm1Koll
(involves: 129 * C57BL/6)
|
abnormal granulocyte differentiation
|
J:71097
|
Il17rbtm1Lex/Il17rbtm1Lex
(C.129-Il17rbtm1Lex)
|
abnormal osteoclast differentiation
|
J:159874
|
Il17retm1Lex/Il17retm1Lex
(B6.129S5-Il17retm1Lex)
|
abnormal intestinal goblet cell morphology
|
J:178967
|
Il18tm1Aki/Il18tm1Aki
(B6.129P2-Il18tm1Aki)
|
impaired neutrophil chemotaxis
|
J:125285
|
Il20ratm1.1Misc/Il20ratm1.1Misc
(involves: C57BL/6)
|
abnormal osteoclast differentiation
|
J:177783
|
Il20rbtm1Uwe/Il20rbtm1Uwe
(B6.129P2-Il20rbtm1Uwe)
|
increased T cell proliferation
|
J:143497
|
Il21rtm1Wjl/Il21rtm1Wjl
(NOD.Cg-Il21rtm1Wjl)
|
decreased T cell proliferation
|
J:139075
|
Il23atm1.1Thak/Il23atm1.1Thak
(C57BL/6-Il23atm1.1Thak)
|
decreased T cell proliferation
|
J:143970
|
Il25tm1Dart/Il25tm1Dart
(C57BL/6-Il25tm1Dart)
|
abnormal intestinal goblet cell morphology
|
J:123808
|
Il27ratm1Mak/Il27ratm1Mak
(B6.129P2-Il27ratm1Mak)
|
increased T cell proliferation
|
J:89509
|
Il31ratm1Ngh/Il31ratm1Ngh
(involves: C57BL/6)
|
increased T cell proliferation
|
J:123198
|
Il33tm1(KOMP)Vlcg/Il33tm1(KOMP)Vlcg
(C57BL/6-Il33tm1(KOMP)Vlcg)
|
abnormal autophagy
|
J:251814,
J:232676
|
abnormal double-strand DNA break repair
|
J:251814
|
impaired macrophage chemotaxis
|
J:232676
|
Il34tm1b(EUCOMM)Wtsi/Il34tm1b(EUCOMM)Wtsi
(involves: BALB/cJ * C57BL/6N)
|
increased neuron apoptosis
|
J:187643
|
Il36gtm1Lex/Il36gtm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
increased macrophage apoptosis
|
J:264077
|
Il36gtm1Lex/Il36gtm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
impaired macrophage phagocytosis
|
J:296074
|
Ildr2W87*/Ildr2W87*
(involves: C3HeB/FeJ)
|
abnormal pancreatic beta cell differentiation
|
J:138216
|
Ilf3tm1Pnk/Ilf3tm1Pnk
(involves: 129S1/Sv * 129X1/SvJ)
|
increased apoptosis
|
J:99935
|
Ilktm1Ref/Ilktm1Ref
(Not Specified)
|
abnormal basement membrane morphology
|
J:82761
|
Ilktm1Star/Ilktm1Star
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased keratinocyte migration
|
J:172934
|
Ilktm1Star/Ilktm1Star Tg(Ckmm-cre)1Lrsn/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
cardiac interstitial fibrosis
|
J:112174
|
Ilktm1Star/Ilktm1Star Tg(KRT14-cre)1Amc/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased keratinocyte proliferation
|
J:172934
|
Ilktm1Star/Ilktm1Star Tg(NPHS2-cre)295Lbh/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
detached podocyte
|
J:129286,
J:129244
|
increased kidney apoptosis
|
J:129286
|
increased podocyte apoptosis
|
J:129286
|
Ilktm3Ref/Ilktm3Ref Tg(Col2a1-cre)1Asz/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal cell adhesion
|
J:110783
|
abnormal cell cycle
|
J:110783
|
decreased cell proliferation
|
J:110783
|
Ilktm9.1Ref/Ilktm9.1Ref
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
increased metanephric mesenchyme apoptosis
|
J:154054
|
Imebt1DU6/?
(involves: DU6 * DUKs)
|
maternal imprinting
|
J:99475
|
Imebt2DU6/?
(involves: DU6 * DUKs)
|
maternal imprinting
|
J:99475
|
Immp2lTg(Tyr)979Ove/Immp2lTg(Tyr)979Ove
(FVB/N-Immp2lTg(Tyr)979Ove)
|
abnormal cellular respiration
|
J:128071
|
abnormal oocyte morphology
|
J:128071
|
abnormal respiratory electron transport chain
|
J:128071
|
decreased oocyte number
|
J:128071
|
oligozoospermia
|
J:128071
|
ImmtGt(AW0256)Wtsi/Immt+
(involves: 129P2/OlaHsd)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:344896
|
abnormal mitochondrial crista morphology
|
J:344896
|
abnormal mitochondrial matrix morphology
|
J:344896
|
abnormal mitochondrial physiology
|
J:344896
|
abnormal muscle fiber mitochondrial morphology
|
J:344896
|
abnormal neuron mitochondrial morphology
|
J:344896
|
abnormal oxidative phosphorylation
|
J:344896
|
increased cellular glucose import
|
J:344896
|
increased cellular sensitivity to X-ray irradiation
|
J:344896
|
increased neuron apoptosis
|
J:344896
|
oxidative stress
|
J:344896
|
ImmtGt(AW0256)Wtsi/ImmtGt(AW0256)Wtsi
(involves: 129P2/OlaHsd)
|
increased embryonic tissue cell apoptosis
|
J:344896
|
Impdh1tm1Bmi/Impdh1tm1Bmi
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased T cell proliferation
|
J:85443
|
Impdh1tm1Bmi/Impdh1tm1Bmi Impdh2tm1Bmi/Impdh2+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased splenocyte proliferation
|
J:85443
|
decreased T cell proliferation
|
J:85443
|
Impg2em1Xjz/Impg2em1Xjz
(C57BL/6J-Impg2em1Xjz)
|
abnormal extracellular matrix morphology
|
J:295355
|
impaired autophagy
|
J:295355
|
increased endoplasmic reticulum stress
|
J:295355
|
In(1)1Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:134667
|
In(1)12Rk/+
(involves: C57BL/6J)
|
abnormal male meiosis
|
J:23389
|
In(1)24Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
In(2)5Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:109968
|
In(2)19Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
In(3)11Rk/+
(involves: C57BL/6J)
|
abnormal male meiosis
|
J:23389
|
In(4)28Rk/+
(involves: M. m. domesticus poschiavinus)
|
abnormal male meiosis
|
J:23389
|
In(4)32Rk/+
(Not Specified)
|
abnormal male meiosis
|
J:23389
|
In(5)2Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:134667,
J:43743
|
In(5)9Rk/+
(involves: C3H * DBA/2J)
|
abnormal male meiosis
|
J:109968
|
In(5)30Rk/+
(involves: M. m. domesticus poschiavinus)
|
abnormal male meiosis
|
J:23389
|
In(5)33Rk/+
(involves: M. m. domesticus poschiavinus)
|
abnormal male meiosis
|
J:23389
|
In(7)13Rk/+
(involves: C3H * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
In(8)14Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
In(9)26Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
In(10)6Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:109968
|
In(10)17Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
In(12)25Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
In(13)31Rk/+
(Not Specified)
|
abnormal male meiosis
|
J:23389
|
In(14)22Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
In(15)18Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:43743
|
In(15)21Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
decreased male germ cell number
|
J:137335
|
In(15)35Rk/+
(involves: C57BL/6J * DBA/2J)
|
abnormal male meiosis
|
J:23389
|
X/In(YLS)Lub
(Not Specified)
|
abnormal chromosome morphology
|
J:148754
|
Inavatm1.1Itl/Inavatm1.1Itl
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
increased cell migration
|
J:257317
|
Inca1tm1Cmt/Inca1tm1Cmt
(involves: 129 * C57BL/6N)
|
decreased fibroblast proliferation
|
J:175667
|
inft4/inft4
(Not Specified)
|
decreased sperm progressive motility
|
J:89386
|
globozoospermia
|
J:89386
|
oligozoospermia
|
J:89386
|
short sperm flagellum
|
J:89386
|
inft8/inft8
(Not Specified)
|
abnormal sperm flagellum morphology
|
J:89386
|
decreased sperm progressive motility
|
J:89386
|
globozoospermia
|
J:89386
|
oligozoospermia
|
J:89386
|
inft9/inft9
(Not Specified)
|
abnormal sperm flagellum morphology
|
J:89386
|
decreased sperm progressive motility
|
J:89386
|
globozoospermia
|
J:89386
|
oligozoospermia
|
J:89386
|
Ing1Gt(F066C08)Irpa/Ing1Gt(F066C08)Irpa
(involves: 129S2/SvPas)
|
cellular phenotype
|
J:126798
|
delayed cellular replicative senescence
|
J:126798
|
increased fibroblast proliferation
|
J:126798
|
Ing1Gt(OST206270)Lex/Ing1Gt(OST206270)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:118602
|
increased cellular sensitivity to ionizing radiation
|
J:118602
|
increased fibroblast apoptosis
|
J:118602
|
increased fibroblast proliferation
|
J:118602
|
increased thymocyte apoptosis
|
J:118602
|
Ing1Gt(OST206270)Lex/Ing1Gt(OST206270)Lex Trp53tm1Brd/Trp53tm1Brd
(involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6)
|
increased cell proliferation
|
J:118602
|
increased cellular sensitivity to ionizing radiation
|
J:118602
|
Ing1tm1Avg/Ing1tm1Avg
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell cycle
|
J:105658
|
increased cellular sensitivity to ultraviolet irradiation
|
J:105658
|
Ing2tm1.1Ccha/Ing2tm1.1Ccha
(involves: 129 * C57BL/6J * FVB/N)
|
abnormal cell physiology
|
J:167311
|
arrest of male meiosis
|
J:167311
|
asthenozoospermia
|
J:167311
|
coiled sperm flagellum
|
J:167311
|
decreased male germ cell number
|
J:167311
|
enlarged sperm head
|
J:167311
|
globozoospermia
|
J:167311
|
increased apoptosis
|
J:167311
|
multiflagellated sperm
|
J:167311
|
multinucleated giant male germ cells
|
J:167311
|
oligozoospermia
|
J:167311
|
short sperm flagellum
|
J:167311
|
teratozoospermia
|
J:167311
|
Ing2tm1.1Ccha/Ing2tm1.1Ccha Trp53tm1Brd/Trp53tm1Brd
(involves: 129 * 129S7/SvEvBrd * C57BL/6J * FVB/N)
|
increased apoptosis
|
J:167311
|
oligozoospermia
|
J:167311
|
Inhaem1Crah/Inha+
(C57BL/6J-Inhaem1Crah)
|
maternal effect
|
J:324311
|
Inhaem1Crah/Inhaem1Crah
(involves: C57BL/6J)
|
abnormal oocyte morphology
|
J:324311
|
maternal effect
|
J:324311
|
Inhatm1Bay/Inhatm1Bay
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased Sertoli cell proliferation
|
J:125349
|
Inhbatm1Zuk/Inhbatm3Zuk Inhbbtm1Jae/Inhbbtm1Jae Amhr2tm3(cre)Bhr/Amhr2+
(involves: 129S4/SvJae * 129S7/SvEvBrd * C57BL/6J)
|
absent oocytes
|
J:125354
|
Ino80tm1Schg/Ino80tm1Schg Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * CBA)
|
abnormal cell cycle
|
J:221224
|
abnormal cell physiology
|
J:221224
|
abnormal DNA repair
|
J:221224
|
abnormal DNA replication
|
J:221224
|
abnormal double-strand DNA break repair
|
J:221224
|
abnormal telomere morphology
|
J:221224
|
cellular phenotype
|
J:221224
|
decreased fibroblast proliferation
|
J:221224
|
early cellular replicative senescence
|
J:221224
|
increased cellular sensitivity to alkylating agents
|
J:221224
|
increased cellular sensitivity to hydroxyurea
|
J:221224
|
increased cellular sensitivity to ultraviolet irradiation
|
J:221224
|
Inpp4btm1.1Jva/Inpp4btm1.1Jva
(B6.129-Inpp4btm1.1Jva)
|
abnormal osteoclast differentiation
|
J:177648
|
Inpp5btm1Nbm/Inpp5btm1Nbm
(129/Sv-Inpp5btm1Nbm)
|
asthenozoospermia
|
J:73678
|
oligozoospermia
|
J:73678
|
Inpp5dtm1.1Wgk/Inpp5dtm1.1Wgk
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal mononuclear cell differentiation
|
J:94861
|
Inpp5dtm1Rkh/Inpp5dtm1Rkh
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal granulocyte differentiation
|
J:48193
|
abnormal macrophage chemotaxis
|
J:48193
|
abnormal monocyte differentiation
|
J:48193
|
Inpp5dtm1Rkh/Inpp5dtm1Rkh
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:173301
|
Inpp5dtm1Rkh/Inpp5dtm1Rkh
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal macrophage chemotaxis
|
J:110864
|
abnormal osteoclast differentiation
|
J:78771
|
decreased apoptosis
|
J:78771
|
enhanced B cell migration
|
J:110864
|
increased mast cell degranulation
|
J:120426
|
Inpp5etm1.2Ssch/Inpp5etm1.2Ssch
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cilium morphology
|
J:152712
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:152712
|
Inpp5fGt(XL571)Byg/Inpp5fGt(XL571)Byg
(involves: 129P2/OlaHsd)
|
increased cardiomyocyte apoptosis
|
J:170072
|
Inpp5jtm1.1Cmit/Inpp5jtm1.1Cmit Tg(MMTV-PyVT)634Mul/0
(involves: C57BL/6)
|
decreased cell migration
|
J:224914
|
Inpp5ktm1Brd/Inpp5k+
(B6.Cg-Inpp5ktm1Brd)
|
increased skeletal muscle cell glucose uptake
|
J:139745
|
Ins1tm1.1(cre)Thor/Ins1+ Med15tm1c(KOMP)Wtsi/Med15tm1c(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal mitochondrial biogenesis
|
J:355262
|
abnormal pancreatic beta cell differentiation
|
J:355262
|
decreased cellular glucose uptake
|
J:355262
|
decreased mitochondrial number
|
J:355262
|
increased mitochondrial size
|
J:355262
|
increased pancreatic beta cell proliferation
|
J:355262
|
Ins1tm1Jja/Ins1tm1Jja Ins2tm1Jja/Ins2tm1Jja
(involves: 129S2/SvPas * C57BL/6)
|
decreased pancreatic islet cell apoptosis
|
J:106827
|
increased pancreatic alpha cell proliferation
|
J:106827
|
increased pancreatic beta cell proliferation
|
J:106827
|
Ins2Akita/?
(involves: C57BL/6NSlc)
|
decreased adipocyte glucose uptake
|
J:130021
|
decreased skeletal muscle cell glucose uptake
|
J:130021
|
increased adipocyte glucose uptake
|
J:130021
|
Ins2Akita/Ins2+
(C57BL/6-Ins2Akita)
|
abnormal mitochondrial morphology
|
J:108948
|
Ins2Akita/Ins2+
(C57BL/6-Ins2Akita/J)
|
increased retina apoptosis
|
J:99412
|
Ins2Akita/Ins2Akita
(involves: C57BL/6NSlc)
|
increased pancreatic islet cell apoptosis
|
J:156725
|
Ins2Akita/Ins2Akita Jazf1tm1c(EUCOMM)Wtsi/Jazf1tm1c(EUCOMM)Wtsi Tg(Ins2-cre)23Herr/0
(involves: 129S4/SvJaeSor * C57BL/6N * C57BL/6NSlc * CBA/J)
|
decreased pancreatic beta cell proliferation
|
J:303318
|
increased pancreatic beta cell apoptosis
|
J:303318
|
Insctm1Jakn/Insctm1Jakn Tg(Nes-cre)1Wmz/0
(involves: C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:178712
|
Insig1tm1.1Aztc/Insig1tm1.1Aztc
(Not Specified)
|
abnormal white fat cell differentation
|
J:208931
|
Insl3tm1Imad/Insl3tm1Imad
(involves: 129/Sv * CD-1)
|
decreased germ cell number
|
J:83429
|
Insl3tm1Par/Insl3tm1Par
(involves: 129/Sv * CD-1)
|
decreased spermatid number
|
J:55881
|
multinucleated giant male germ cells
|
J:55881
|
Insl5tm1Imad/Insl5tm1Imad
(129(B6)-Insl5tm1Imad)
|
asthenozoospermia
|
J:189146
|
Insl6tm1Imad/Insl6tm1Imad
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1)
|
abnormal male germ cell apoptosis
|
J:157348
|
abnormal male germ cell morphology
|
J:157348
|
asthenozoospermia
|
J:157348
|
azoospermia
|
J:157348
|
oligozoospermia
|
J:157348
|
Insm1tm1.1(GFP/cre)Mgn/Insm1tm1.1(GFP/cre)Mgn
(involves: 129S6/SvEvTac * CD-1 * SJL)
|
decreased pancreatic endocrine progenitor cell proliferation
|
J:214095
|
Insm1tm1.1Jga/Insm1tm1.1Jga
(either: B6.129P2-Insm1tm1.1Jga or (involves: 129P2/OlaHsd * C57BL/6 * CD-1 * FVB/N))
|
abnormal neuron differentiation
|
J:168833
|
increased neuron apoptosis
|
J:168833
|
Insm1tm1Cbm/Insm1tm1Cbm
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
increased pancreas apoptosis
|
J:112173
|
Insrtm1Khn/Insrtm1Khn Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S4/SvJae * C57BL/6J * DBA/2 * FVB)
|
increased mitochondrial size
|
J:63878
|
Insrtm1Khn/Insrtm1Khn Tg(Myhca-cre)1Abel/0
(involves: 129S4/SvJae * FVB)
|
abnormal cardiac muscle cell glucose uptake
|
J:75348
|
decreased cardiac muscle cell glucose uptake
|
J:75348
|
increased cardiac muscle cell glucose uptake
|
J:75348
|
Insrtm1Khn/Insrtm1Khn Tg(Nes-cre)1Kln/0
(involves: 129S4/SvJae * C57BL/6J * SJL)
|
oligozoospermia
|
J:64790
|
Intudtm/Intudtm
(involves: C3H/HeN)
|
abnormal cilium morphology
|
J:222441
|
abnormal embryonic neuroepithelium primary cilium morphology
|
J:222441
|
abnormal kidney epithelial cell primary cilium morphology
|
J:222441
|
decreased embryonic cilium length
|
J:222441
|
decreased embryonic cilium number
|
J:222441
|
Intutm1.2Aliu/Intutm1.2Aliu
(involves: 129P2/OlaHsd * 129S4/SvJae * C3H)
|
abnormal cilium morphology
|
J:159120
|
decreased embryonic cilium length
|
J:159120
|
Intutm1.2Aliu/Intutm1.2Aliu
(involves: 129P2/OlaHsd * C3H/HeN)
|
abnormal cell morphology
|
J:222441
|
Invsinv/Invsinv
(involves: FVB/N)
|
abnormal embryonic cilium location or orientation
|
J:109561
|
abnormal motile primary cilium physiology
|
J:109561
|
Ip6k1em1Seyk/Ip6k1em1Seyk
(C57BL/6-Ip6k1em1Seyk)
|
abnormal endocytosis
|
J:306957
|
abnormal synaptic vesicle exocytosis
|
J:306957
|
Ip6k1Gt(OST137568)Lex/Ip6k1Gt(OST137568)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
azoospermia
|
J:103485
|
Ip6k1tm1.1Snyd/Ip6k1tm1.1Snyd
(involves: 129X1/SvJ * BALB/c * C57BL/6)
|
azoospermia
|
J:132167
|
decreased elongated spermatid number
|
J:132167
|
Ip6k2tm1.1Snyd/Ip6k2tm1.1Snyd
(B6.129-Ip6k2tm1.1Snyd)
|
decreased cellular sensitivity to ionizing radiation
|
J:212482
|
decreased sensitivity to induced cell death
|
J:212482
|
Ip6k2tm1Dlin/Ip6k2tm1Dlin
(involves: 129X1/SvJ * Black Swiss * C57BL/6)
|
abnormal cell death
|
J:151345
|
abnormal double-strand DNA break repair
|
J:151345
|
increased fibroblast proliferation
|
J:151345
|
Iqcf1em1Zdq/Iqcf1em1Zdq
(Not Specified)
|
asthenozoospermia
|
J:228595
|
Iqcgesgd12d/Iqcgesgd12d
(involves: C3HeB/FeJ * C57BL/6)
|
absent sperm flagellum
|
J:92463
|
asthenozoospermia
|
J:92463
|
azoospermia
|
J:86161
|
oligozoospermia
|
J:92463
|
short sperm flagellum
|
J:92463
|
teratozoospermia
|
J:92463
|
Iqcgesgd12d/Iqcgesgd12d
(involves: C57BL/6)
|
azoospermia
|
J:218515
|
Iqcgesgd12d/Iqcgtm1b(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N * FVB/NJ)
|
azoospermia
|
J:218515
|
Iqcgtm1a(EUCOMM)Wtsi/Iqcgtm1a(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
abnormal sperm axoneme morphology
|
J:216319
|
abnormal sperm flagellum morphology
|
J:216319
|
abnormal sperm head morphology
|
J:216319
|
abnormal sperm nucleus morphology
|
J:216319
|
cellular phenotype
|
J:216319
|
immotile sperm
|
J:216319
|
short sperm flagellum
|
J:216319
|
Iqcgtm1b(EUCOMM)Wtsi/Iqcgtm1b(EUCOMM)Wtsi
(involves: C57BL/6N * FVB/NJ)
|
azoospermia
|
J:218515
|
Iqchem2Alfon/Iqchem2Alfon
(involves: C57BL/6 * CBA)
|
abnormal acrosome morphology
|
J:338977
|
abnormal sperm flagellum morphology
|
J:338977
|
abnormal sperm head morphology
|
J:338977
|
abnormal sperm midpiece morphology
|
J:338977
|
asthenozoospermia
|
J:338977
|
oligozoospermia
|
J:338977
|
teratozoospermia
|
J:338977
|
Iqcnem1Cya/Iqcnem1Cya
(C57BL/6J-Iqcnem1Cya)
|
abnormal acrosome morphology
|
J:332231
|
abnormal sperm head morphology
|
J:332231
|
ectopic manchette
|
J:332231
|
elongated manchette
|
J:332231
|
Iqgap2tm1Vs/Iqgap2tm1Vs
(either: 129S4/SvJae-Iqgap2tm1Vs or B6.129S4-Iqgap2tm1Vs)
|
abnormal hepatocyte mitochondrial morphology
|
J:132670
|
increased hepatocyte apoptosis
|
J:132670
|
Iqubem1Mngx/Iqubem1Mngx
(C57BL/6J-Iqubem1Mngx)
|
abnormal sperm flagellum morphology
|
J:332237
|
asthenozoospermia
|
J:332237
|
cellular phenotype
|
J:332237
|
decreased sperm progressive motility
|
J:332237
|
Irak1tm1Wpfl/Irak1tm1Wpfl
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:110860
|
Irak4tm1Aki/Irak4tm1Aki
(involves: 129X1/SvJ * C57BL/6)
|
decreased B cell proliferation
|
J:125729
|
Irak4tm1Gram/Irak4tm1Gram
(involves: BALB/c)
|
abnormal fibroblast physiology
|
J:121912
|
Irak4tm1Yeh/Irak4tm1Yeh
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased B cell proliferation
|
J:76098
|
Irak4tm2Aki/Irak4tm2Aki
(involves: 129X1/SvJ * C57BL/6)
|
decreased B cell proliferation
|
J:125729
|
Irf1tm1Cwe/Irf1tm1Cwe
(involves: 129)
|
abnormal T cell proliferation
|
J:84367
|
Irf1tm1Mak/Irf1tm1Mak
(involves: 129S2/SvPas)
|
abnormal DNA repair
|
J:115104
|
cellular phenotype
|
J:115104
|
Irf2tm1Mak/Irf2tm1Mak
(either: (involves: 129S2/SvPas * C57BL/6J) or (involves: 129S2/SvPas * C57BL/6J * DBA/2))
|
decreased B cell proliferation
|
J:64286
|
Irf3tm1Ttg/Irf3tm1Ttg
(involves: 129S/SvEv * C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:150948
|
Irf4tm1.1Rdf/Irf4tm1.1Rdf
(involves: 129S1/Sv * 129S4/SvJae * C57BL/6)
|
decreased B cell proliferation
|
J:112643
|
Irf4tm1Mak/Irf4tm1Mak
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:42683
|
decreased T cell proliferation
|
J:42683
|
Irf4tm1Rdf/Irf4tm1Rdf Tg(Ucp1-cre)1Evdr/0
(involves: 129S1/Sv * C57BL/6J * FVB)
|
abnormal cellular respiration
|
J:214637
|
decreased fatty acid oxidation
|
J:214637
|
Irf6Gt(OST398253)Lex/Irf6Gt(OST398253)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:115343
|
increased keratinocyte proliferation
|
J:115343
|
Irf9M1Btlr/Irf9+
(C57BL/6J-Irf9M1Btlr)
|
increased cell death
|
J:236674
|
Irf9M1Btlr/Irf9M1Btlr
(C57BL/6J-Irf9M1Btlr)
|
increased cell death
|
J:236674
|
Irgcem1Osb/Irgcem1Osb
(B6;D2-Irgcem1Osb/Osb)
|
abnormal sperm fibrous sheath morphology
|
J:326368
|
decreased sperm progressive motility
|
J:326368
|
short sperm flagellum
|
J:326368
|
Irs1Sml/Irs1Sml
(C3.Cg-Irs1Sml H2b/GrsrJ)
|
decreased osteoblast proliferation
|
J:163661
|
impaired osteoblast differentiation
|
J:163661
|
Irs1tm1Tka/Irs1tm1Tka
(involves: C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:68004
|
abnormal osteoblast physiology
|
J:61479
|
abnormal osteoclast differentiation
|
J:61479
|
decreased cell proliferation
|
J:89532
|
Irs1tm1Tka/Irs1tm1Tka Irs2tm1Tka/Irs2tm1Tka
(involves: C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:68004
|
Irs2tm1.1With/Irs2tm1.1With
(B6.129S6-Irs2tm1.1With)
|
decreased granulosa cell proliferation
|
J:122064
|
Irs2tm1Mfw/Irs2tm1Mfw
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal oogenesis
|
J:64791
|
decreased oocyte number
|
J:64791
|
Irs2tm1Tka/Irs2tm1Tka
(involves: C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:68004
|
Is(In8B2-8B3.1;6C1)1Tshir/Is(In8B2-8B3.1;6C1)1Tshir
(involves: A/WySn * C57BL/10 * M. m. molossinus * NZB)
|
patent ductus arteriosus
|
J:198239
|
Isl1tm1.1Whk/Isl1tm1.1Whk Tg(Six3-cre)69Frty/0
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * DBA/2)
|
increased retina apoptosis
|
J:146349
|
Itchtm1.1Alta/Itchtm1.1Alta Foxp3tm4(YFP/icre)Ayr/Foxp3+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased regulatory T cell apoptosis
|
J:204685
|
Itga1tm1Gdnr/Itga1tm1Gdnr
(involves: 129S4/SvJae * BALB/c)
|
increased renal glomerulus apoptosis
|
J:91522
|
Itga2tm1.1Eck/Itga2tm1.1Eck
(B6.129P2-Itga2tm1.1Eck)
|
abnormal cell adhesion
|
J:108931
|
Itga2tm1Ztr/Itga2tm1Ztr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell adhesion
|
J:77798
|
Itga2btm1(GFP/cre)Emam/Itga2btm1(GFP/cre)Emam
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell adhesion
|
J:84564
|
Itga2btm1(GFP/cre)Emam/Itga2btm1(GFP/cre)Emam Rhoatm1Csab/Rhoatm1Csab Tg(ITGA2B)3Mako/0 Tg(Pf4-icre)Q3Rsko/0
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:204459
|
Itga4tm1Leg/Itga4tm1Leg
(Not Specified)
|
abnormal cell physiology
|
J:151371
|
Itga4tm1Mgin/Itga4tm1Mgin
(B6.129-Itga4tm1Mgin)
|
impaired macrophage chemotaxis
|
J:106471
|
Itga4tm1Mgin/Itga4tm1Mgin
(Not Specified)
|
abnormal cell physiology
|
J:151371
|
Itga4tm1Mshi/Itga4tm1Mshi
(C57BL/6-Itga4tm1Mshi)
|
abnormal cellular extravasation
|
J:144092
|
abnormal leukocyte adhesion
|
J:144092
|
abnormal leukocyte migration
|
J:144092
|
Itga5tm1Hyn/Itga5tm1Hyn
(involves: 129S2/SvPas * C57BL/6J)
|
cellular phenotype
|
J:16248
|
Itga5tm1Hyn/Itga5tm2Hyn Tg(H2-K1-tsA58)6Kio/0 Tg(Tek-cre)1Ywa/0
(involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca * SJL)
|
abnormal cell adhesion
|
J:161850
|
Itga5tm2Hyn/Itga5tm2Hyn
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuronal migration
|
J:159465
|
Itga5tm2Hyn/Itga5tm2Hyn Itgavtm2Hyn/Itgavtm2Hyn Tg(H2-K1-tsA58)6Kio/0
(involves: 129 * C57BL/6 * SJL)
|
abnormal cell adhesion
|
J:161850
|
Itga5tm2Hyn/Itga5tm2Hyn Tg(Tek-cre)1Ywa/0
(B6.Cg-Tg(Tek-cre)1Ywa Itga5tm2Hyn)
|
patent ductus arteriosus
|
J:161850
|
Itga6tm1Egl/Itga6tm1Egl
(either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129S2/SvPas * C57BL/6 * CD-1))
|
abnormal neuronal precursor cell migration
|
J:79739
|
Itga6tm1Egl/Itga6tm1Egl
(involves: 129S2/SvPas * C57BL/6)
|
abnormal basement membrane morphology
|
J:119018
|
Itga7tm1Umr/Itga7tm1Umr Sgcgtm1Mcn/Sgcgtm1Mcn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:91880
|
increased apoptosis
|
J:91880
|
Itga8tm1Lfr/Itga8tm1Lfr
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell adhesion
|
J:154459
|
abnormal cell migration
|
J:154459
|
Itga11tm1Dgul/Itga11tm1Dgul
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell adhesion
|
J:122349
|
decreased cell proliferation
|
J:122349
|
Itgadtm1Bll/Itgadtm1Bll
(B6.129S7-Itgadtm1Bll)
|
decreased T cell proliferation
|
J:90954
|
Itgaltm1.1Mshi/Itgaltm1.1Mshi
(involves: C57BL/6)
|
abnormal diapedesis
|
J:168533
|
abnormal leukocyte adhesion
|
J:168533
|
abnormal leukocyte migration
|
J:168533
|
enhanced leukocyte tethering or rolling
|
J:168533
|
Itgaltm1Bll/Itgaltm1Bll
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal cellular extravasation
|
J:83226
|
abnormal leukocyte adhesion
|
J:83226
|
abnormal leukocyte migration
|
J:83226
|
Itgaltm1Bll/Itgaltm1Bll
(B6.129S7-Itgaltm1Bll)
|
abnormal leukocyte adhesion
|
J:100242
|
abnormal leukocyte tethering or rolling
|
J:100242
|
decreased T cell proliferation
|
J:90954
|
Itgaltm1Bll/Itgaltm1Bll
(involves: 129S7/SvEvBrd)
|
abnormal cellular extravasation
|
J:141063
|
abnormal leukocyte adhesion
|
J:141063
|
Itgaltm1Hlz/Itgaltm1Hlz
(involves: 129P2/OlaHsd)
|
abnormal cellular extravasation
|
J:99286
|
abnormal leukocyte adhesion
|
J:99286
|
Itgaltm1Hogg/Itgaltm1Hogg
(involves: 129P2/OlaHsd)
|
abnormal leukocyte adhesion
|
J:82587
|
abnormal leukocyte migration
|
J:82587
|
Itgamtm1Bll/Itgamtm1Bll
(B6.129S7-Itgamtm1Bll)
|
abnormal leukocyte adhesion
|
J:100242
|
decreased T cell proliferation
|
J:90954
|
Itgamtm1Bll/Itgamtm1Bll
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal cellular extravasation
|
J:83226
|
abnormal leukocyte adhesion
|
J:83226
|
abnormal leukocyte migration
|
J:83226
|
impaired neutrophil phagocytosis
|
J:39092
|
Itgamtm1Myd/Itgamtm1Myd
(involves: 129S4/SvJae * BALB/c * C57BL/6)
|
abnormal leukocyte adhesion
|
J:38052
|
decreased apoptosis
|
J:38052
|
impaired neutrophil phagocytosis
|
J:38052
|
Itgamtm1Myd/Itgamtm1Myd
(involves: 129S4/SvJae)
|
impaired leukocyte tethering or rolling
|
J:198197
|
impaired neutrophil phagocytosis
|
J:155479
|
Itgamtm1Rws/Itgamtm1Rws
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell adhesion
|
J:65847
|
Itgavtm1Blb/Itgavtm1Blb Itgb1tm1Ref/Itgb1tm1Ref Itgb2tm2Bay/Itgb2tm2Bay Itgb7tm1Cgn/Itgb7tm1Cgn Tg(Mx1-cre)1Cgn/0
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal cellular extravasation
|
J:134784
|
Itgavtm2Hyn/Itgavtm2.1Hyn Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * FVB)
|
impaired macrophage phagocytosis
|
J:125508
|
Itgavtm2Hyn/Itgavtm2.1Hyn Tg(Tek-cre)1Ywa/?
(involves: 129S2/SvPas * C57BL/6 * FVB * SJL)
|
abnormal dendritic cell differentiation
|
J:125508
|
impaired macrophage phagocytosis
|
J:125508
|
Itgaxtm1Bll/Itgaxtm1Bll
(B6.129S7-Itgaxtm1Bll)
|
increased T cell proliferation
|
J:122187
|
Itgb1tm1Efu/Itgb1tm1Efu Tg(KRT14-cre)1Efu/0
(involves: 129X1/SvJ)
|
abnormal basement membrane morphology
|
J:65039
|
Itgb1tm1Efu/Itgb1tm1Efu Tg(NPHS2-cre)295Lbh/0
(involves: 129X1/SvJ * C57BL/6 * SJL)
|
increased mesangial cell number
|
J:135414
|
increased podocyte apoptosis
|
J:135414
|
Itgb1tm1Ehi/Itgb1tm1Ehi
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal cell cycle
|
J:76216
|
decreased cell proliferation
|
J:76216
|
decreased fibroblast proliferation
|
J:76216
|
increased apoptosis
|
J:76216
|
Itgb1tm1Lscd/Itgb1tm1Ref Tg(PLAT-cre)116Sdu/0
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal enteric neural crest cell migration
|
J:108439
|
abnormal neuronal migration
|
J:108439
|
Itgb1tm1Mll/Itgb1tm1Mll Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas * 129X1/SvJ)
|
abnormal radial glial cell morphology
|
J:170581
|
radial glial endfoot detachment
|
J:170581
|
Itgb1tm1Mll/Itgb1tm1Mll Tg(Nes-cre)1Kln/0
(involves: 129X1/SvJ * C57BL/6 * SJL)
|
abnormal neuronal precursor cell migration
|
J:120076
|
Itgb1tm1Ref/Itgb1tm1Ref Tg(Col2a1-cre)1Asz/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased chondrocyte proliferation
|
J:85994
|
increased chondrocyte apoptosis
|
J:85994
|
Itgb1tm1Ref/Itgb1tm1Ref Tg(Ins2-cre)1Heed/? Tg(RIP1-Tag)2Dh/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA * DBA/2J)
|
abnormal cell adhesion
|
J:122649
|
abnormal cell death
|
J:122649
|
abnormal cell morphology
|
J:122649
|
abnormal mitosis
|
J:122649
|
early cellular replicative senescence
|
J:122649
|
Itgb1tm1Ref/Itgb1tm2Ref Tg(Col2a1-cre)1Asz/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased chondrocyte proliferation
|
J:85994
|
increased chondrocyte apoptosis
|
J:85994
|
Itgb1tm1Ref/Itgb1tm5.1Ref Tg(KRT5-cre)5132Jlj/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J)
|
decreased keratinocyte proliferation
|
J:148885
|
Itgb1tm1Ref/Itgb1tm12.1Ref Tg(KRT5-cre)5132Jlj/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J)
|
decreased keratinocyte adhesion
|
J:177979,
J:203018
|
Itgb1tm1Ref/Itgb1tm14.1Ref Tg(KRT5-cre)5132Jlj/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J)
|
decreased keratinocyte migration
|
J:203018
|
Itgb1tm1Ref/Itgb1tm15.1Ref Tg(KRT5-cre)5132Jlj/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J)
|
decreased keratinocyte adhesion
|
J:203018
|
decreased keratinocyte proliferation
|
J:203018
|
Itgb1tm1Ross/Itgb1tm1Ross Myl2tm1(cre)Krc/Myl2+
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss)
|
abnormal cardiac muscle cell glucose uptake
|
J:82534
|
Itgb1tm1Ross/Itgb1tm1Ross Tg(Hoxb7-cre)13Amc/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased kidney apoptosis
|
J:149831
|
increased kidney cell proliferation
|
J:149831
|
Itgb1tm2Son/Itgb1tm2Son
(either: 129P2/OlaHsd-Itgb1tm2Son or (involves: 129P2/OlaHsd * FVB))
|
abnormal cell adhesion
|
J:47279
|
decreased fibroblast cell migration
|
J:47279
|
Itgb1tm11.1Ref/Itgb1tm11.1Ref
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased keratinocyte adhesion
|
J:176453
|
Itgb1tm14.1Ref/Itgb1tm14.1Ref
(Not Specified)
|
abnormal cell physiology
|
J:203018
|
Itgb1tm14.1Ref/Itgb1tm15.1Ref
(Not Specified)
|
abnormal cell physiology
|
J:203018
|
Itgb1tm15.1Ref/Itgb1tm15.1Ref
(Not Specified)
|
abnormal cell physiology
|
J:203018
|
Itgb2tm1.1Arte/Itgb2tm1.1Arte
(involves: C57BL/6NTac)
|
decreased T cell proliferation
|
J:202261
|
Itgb2tm2Bay/Itgb2tm2Bay
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal T cell proliferation
|
J:48542
|
Itgb2tm2Bay/Itgb2tm2Bay
(involves: 129S7/SvEvBrd)
|
decreased T cell proliferation
|
J:90954
|
Itgb2tm2Bay/Itgb2tm2Bay
(B6.129S7-Itgb2tm2Bay)
|
abnormal leukocyte adhesion
|
J:83226
|
abnormal leukocyte migration
|
J:83226
|
Itgb3tm1Hyn/Itgb3tm1.1Wlbcr Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6)
|
abnormal osteoclast differentiation
|
J:224675
|
Itgb3tm1Hyn/Itgb3tm1Hyn
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell adhesion
|
J:73752
|
abnormal cell migration
|
J:73752
|
impaired macrophage chemotaxis
|
J:119666
|
Itgb3tm1Hyn/Itgb3tm1Hyn
(involves: 129S2/SvPas)
|
decreased keratinocyte proliferation
|
J:96049
|
Itgb3tm1Hyn/Itgb3tm1Hyn
(involves: 129S2/SvPas * BALB/c)
|
maternal effect
|
J:131241
|
Itgb4tm1Fgg/Itgb4tm1Fgg
(involves: 129S1/Sv * C57BL/6)
|
abnormal enterocyte proliferation
|
J:48924
|
decreased keratinocyte adhesion
|
J:48924
|
Itgb5tm1Des/Itgb5tm1Des
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal keratinocyte differentiation
|
J:59991
|
Itgb7tm1Cgn/Itgb7tm1Cgn
(involves: C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:34306
|
Itgb7tm1Cgn/Itgb7tm1Cgn
(C57BL/6-Itgb7tm1Cgn/J)
|
abnormal leukocyte migration
|
J:127413
|
Itgb7tm1Mshi/Itgb7tm1Mshi
(involves: C57BL/6)
|
abnormal leukocyte adhesion
|
J:127413
|
abnormal leukocyte migration
|
J:127413
|
Itgb8tm1Lfr/Itgb8tm1Lfr
(either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6J))
|
abnormal radial glial cell morphology
|
J:77682
|
impaired basement membrane formation
|
J:77682
|
Itih4tm1Mish/Itih4tm1Mish Sptbn1tm1Mish/Sptbn1+
(involves: 129S6/SvEvTac * C57BL/6 * NIH Black Swiss)
|
decreased hepatocyte apoptosis
|
J:132133
|
decreased hepatocyte proliferation
|
J:132133
|
Itih5tm1Jmba/Itih5tm1Jmba
(involves: BALB/cJ)
|
abnormal fat cell differentiation
|
J:359016
|
decreased keratinocyte proliferation
|
J:359049
|
Itkm1Btlr/Itkm1Btlr
(C57BL/6J-Itkm1Btlr)
|
abnormal cell proliferation
|
J:236673
|
increased CD8-positive, alpha-beta memory T cell proliferation
|
J:236673
|
Itktm1Litt/Itktm1Litt
(involves: 129S4/SvJae * C57BL/6J)
|
decreased T cell proliferation
|
J:31230
|
Itktm1Litt/Itktm1Litt
(involves: 129S4/SvJae)
|
decreased T cell proliferation
|
J:54449
|
Itktm1Litt/Itktm1Litt
(B6.129S4-Itktm1Litt)
|
decreased T cell proliferation
|
J:141390
|
Itktm1Litt/Itktm1Litt Txktm1Pls/Txktm1Pls
(involves: 129S4/SvJae * 129S6/SvEvTac)
|
decreased T cell proliferation
|
J:54449
|
Itktm1Litt/Itktm1Litt Vav1tm2Bbd/Vav1tm2Bbd
(B6.129-Itktm1Litt Vav1tm2Bbd)
|
increased T cell apoptosis
|
J:141390
|
Itln1em1Cya/Itln1em1Cya
(involves: C57BL/6)
|
decreased osteoblast proliferation
|
J:282124
|
Itpatm1Skmi/Itpatm1Skmi
(involves: 129S/SvEv * C57BL/6J)
|
abnormal cell physiology
|
J:169285
|
decreased male germ cell number
|
J:169285
|
Itpr1opt/Itpr1opt
(involves: C57BLKS)
|
abnormal cell physiology
|
J:50383
|
Itprid2tm1Sawa/Itprid2tm1Sawa
(B6.Cg-Itprid2tm1Sawa)
|
increased adipocyte glucose uptake
|
J:144968
|
Itpriptm1.1Snyd/Itpriptm1.1Snyd
(involves: C57BL/6)
|
abnormal cell physiology
|
J:157643
|
increased sensitivity to induced cell death
|
J:157643
|
Itpripl1em1Smoc/Itpripl1em1Smoc
(C57BL/6J-Itpripl1em1Smoc)
|
asthenozoospermia
|
J:348064
|
Itsn1tm1.1Mapr/Itsn1tm1.1Mapr
(involves: 129S6/SvEvTac * 129X1/SvJ)
|
abnormal cell morphology
|
J:140030
|
Itsn1tm2.1Mapr/Itsn1tm2.1Mapr
(involves: 129S6/SvEvTac * 129X1/SvJ)
|
abnormal cell morphology
|
J:140030
|
Ivns1abptm1Htno/Ivns1abptm1Htno
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:162743
|
increased sensitivity to induced cell death
|
J:162743
|
Izumo3tm1Osb/Izumo3tm1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal acrosome morphology
|
J:324147
|
Jag1Ndr/Jag1Ndr
(involves: C3HeB/FeJ)
|
abnormal neuron differentiation
|
J:156172
|
Jag1tm1Grid/Jag1tm2Grid Tg(Tagln-cre)1Her/0
(involves: 129S1/Sv * C57BL/6 * SJL)
|
patent ductus arteriosus
|
J:166769
|
Jagn1tm1c(EUCOMM)Hmgu/Jagn1tm1c(EUCOMM)Hmgu Commd10Tg(Vav1-icre)A2Kio/Commd10+
(involves: C57BL/6N * C57BL/10 * CBA/Ca)
|
impaired neutrophil chemotaxis
|
J:214828
|
Jak2tm1(JAK2)Argr/Jak2+ Tg(Mx1-cre)1Cgn/0
(involves: 129S7/SvEvBrd * C57BL/6 * CBA)
|
abnormal megakaryocyte differentiation
|
J:164539
|
Jak2tm1Jni/Jak2tm1Jni
(involves: 129P2/OlaHsd)
|
abnormal megakaryocyte differentiation
|
J:47299
|
Jak2tm2.1Kpf/Jak2tm2.1Kpf
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:207710
|
Jak3tm1Flv/Jak3tm1Flv
(involves: 129S1/Sv)
|
abnormal T cell proliferation
|
J:95794
|
Jak3tm1Ljb/Jak3tm1Ljb
(involves: 129S4/SvJae * C57BL/6)
|
decreased T cell proliferation
|
J:29722
|
Jak3tm1Ljb/Jak3tm1Ljb
(involves: 129S4/SvJae)
|
decreased T cell proliferation
|
J:128694
|
Jak3tm1Ljb/Jak3tm1Ljb
(B6;129S4-Jak3tm1Ljb/J)
|
abnormal dendritic cell differentiation
|
J:123902
|
Jak3tm1Ljb/Jak3tm1Ljb Tg(Lck-Jak3)1Ljb/0
(involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/10)
|
decreased T cell proliferation
|
J:128694
|
Jak3tm1Ljb/Jak3tm1Ljb Tg(Lck-Jak3)2Ljb/0
(involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/10)
|
decreased T cell proliferation
|
J:128694
|
Jam3tm1Lex/Jam3tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
azoospermia
|
J:145994,
J:281813
|
Jam3tm1Rha/Jam3tm1.1Chav Tg(Spo11-cre)D5Mpel/0
(involves: 129P2/OlaHsd * BALB/c * C57BL/6)
|
abnormal manchette morphology
|
J:166888
|
decreased male germ cell number
|
J:166888
|
decreased spermatid number
|
J:166888
|
increased male germ cell apoptosis
|
J:166888
|
Jam3tm1Rha/Jam3tm1Rha
(involves: 129P2/OlaHsd * C57BL/6)
|
globozoospermia
|
J:92665
|
Jamltm1Fnyi/Jamltm1Fnyi Tg(NPHS2-cre)295Lbh/0
(B6.Cg-Jamltm1Fnyi Tg(NPHS2-cre)295Lbh)
|
increased podocyte apoptosis
|
J:300243
|
Jarid2Gt(ROSA)1Gel/Jarid2Gt(ROSA)1Gel
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:100923
|
Jazf1tm1c(EUCOMM)Wtsi/Jazf1tm1c(EUCOMM)Wtsi Tg(Ins2-cre)23Herr/0
(involves: 129S4/SvJaeSor * C57BL/6N * CBA/J)
|
abnormal translation
|
J:303318
|
Jdp2tm1Aki/Jdp2tm1Aki
(Not Specified)
|
abnormal osteoclast differentiation
|
J:191061
|
Jdp2tm1Kkyo/Jdp2tm1Kkyo
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell differentiation
|
J:139241
|
Jdp2tm1Kkyo/Jdp2tm1Kkyo
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle
|
J:166559
|
increased cell proliferation
|
J:166559
|
JhyTg(Dlk1-lacZ)#aJvs/JhyTg(Dlk1-lacZ)#aJvs
(involves: FVB/N)
|
abnormal brain ependyma motile cilium location or orientation
|
J:202225
|
abnormal brain ependyma motile cilium morphology
|
J:202225
|
decreased brain ependyma motile cilium length
|
J:202225
|
decreased brain ependyma motile cilium number
|
J:202225
|
Jmjd1ctm1Mtac/Jmjd1ctm1Mtac
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
decreased male germ cell number
|
J:203917
|
decreased spermatogonia number
|
J:203917
|
increased male germ cell apoptosis
|
J:203917
|
oligozoospermia
|
J:203917
|
Jmjd6tm1Gbf/Jmjd6tm1Gbf
(C57BL/6-Ptdsrtm1Gbf)
|
cellular phenotype
|
J:98905
|
Jmjd8em1Kaso/Jmjd8em1Kaso
(C57BL/6-Jmjd8em1Kaso)
|
increased adipocyte glucose uptake
|
J:319518
|
Jmjd8tm1(KOMP)Vlcg/Jmjd8tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal cellular respiration
|
J:246535
|
Jmytm1Smoc/Jmytm1Smoc Tg(Amh-cre)8815Reb/0
(involves: 129S * C57BL/6)
|
asthenozoospermia
|
J:307721
|
decreased sperm progressive motility
|
J:307721
|
enlarged sperm head
|
J:307721
|
oligozoospermia
|
J:307721
|
Juntm1Bdc/Juntm1Bdc
(Not Specified)
|
decreased neuron apoptosis
|
J:78265
|
Juntm1Pa/Juntm1Pa
(either: (involves: 129S/SvEv * 129X1/SvJ) or (involves: 129X1/SvJ * C57BL/6J))
|
decreased fibroblast proliferation
|
J:13175
|
Juntm1Rsjo/Juntm1Rsjo Tg(KRT14-cre)8Brn/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
decreased keratinocyte proliferation
|
J:84743
|
Juntm1Wag/Juntm1Wag
(involves: 129S2/SvPas)
|
decreased cell proliferation
|
J:175212
|
oxidative stress
|
J:175212
|
Juntm1Wag/Juntm1Wag
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cardiac neural crest cell migration
|
J:55508
|
decreased hepatocyte proliferation
|
J:55508
|
increased hepatocyte apoptosis
|
J:55508
|
Juntm1Wag/Juntm1Wag
(either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6))
|
increased hepatocyte apoptosis
|
J:14538
|
Juntm1Wag/Juntm1Wag Tg(Junb)1598Angl/0
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell proliferation
|
J:75359
|
Juntm2.1Wag/Juntm2.1Wag
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased cell proliferation
|
J:53481
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:53481
|
decreased susceptibility to neuronal excitotoxicity
|
J:53481
|
Juntm4Wag/Juntm4Wag Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
decreased neuron apoptosis
|
J:176956
|
Juntm4Wag/Juntm4Wag Tg(Sftpc-cre)1Blh/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
increased lung apoptosis
|
J:179883
|
Juntm5.1(Junb)Wag/Juntm5.1(Junb)Wag
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell proliferation
|
J:75359
|
Juntm6.1(Jund)Wag/Juntm6.1(Jund)Wag
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:175212
|
oxidative stress
|
J:175212
|
Juntm6.1(Jund)Wag/Juntm6.1(Jund)Wag Jundtm1Mya/Jundtm1Mya
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
decreased fibroblast proliferation
|
J:175212
|
early cellular replicative senescence
|
J:175212
|
Junbtm3Wag/Junbtm3Wag Meox2tm1(cre)Sor/Meox2+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6)
|
abnormal osteoclast differentiation
|
J:88126
|
Junbtm3Wag/Junbtm3Wag Tg(KRT5-cre)1Tak/0
(involves: 129/Sv * 129P2/OlaHsd * C3H * C57BL/6)
|
increased mesangial cell number
|
J:155575
|
Jundtm1Mya/Jundtm1Mya
(either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6))
|
abnormal cell cycle
|
J:65879
|
asthenozoospermia
|
J:53906
|
decreased fibroblast proliferation
|
J:65879
|
increased cell proliferation
|
J:65879
|
increased cellular sensitivity to ultraviolet irradiation
|
J:65879
|
increased T cell proliferation
|
J:89085
|
oligozoospermia
|
J:53906
|
teratozoospermia
|
J:53906
|
Jundtm1Mya/Jundtm1Mya Tg(H2-K-Fosl1)1Wag/0
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
abnormal mitochondrial physiology
|
J:95691
|
cardiac interstitial fibrosis
|
J:95691
|
Juptm1.1Shou/Juptm1.1Shou Tg(Myh6-cre)2182Mds/0
(involves: 129 * C57BL/6J)
|
increased cardiomyocyte apoptosis
|
J:177567
|
Juptm1Ruiz/Jup+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal fat cell differentiation
|
J:192719
|
Kank4em1Jhhu/Kank4em1Jhhu
(C57BL/6J-Kank4em1Jhhu)
|
decreased endothelial cell proliferation
|
J:326312
|
Kansl1em1.1Cya/Kansl1+
(B6(FVB)-Kansl1em1.1Cya)
|
abnormal autophagy
|
J:327464
|
oxidative stress
|
J:327464
|
Kansl1em1.1Cya/Kansl1em1.1Cya
(B6(FVB)-Kansl1em1.1Cya)
|
abnormal autophagy
|
J:327464
|
Kansl1em1Cya/Kansl1+ Tg(CAG-cre/Esr1*)5Amc/0
(Not Specified)
|
abnormal autophagy
|
J:327464
|
Kansl1em1Cya/Kansl1+ Tg(CAG-cre/Esr1*)5Amc/0 Igs2tm1(CAG-mt-Keima)Fink/Igs2+
(Not Specified)
|
abnormal mitophagy
|
J:327464
|
Kansl1em1Cya/Kansl1em1Cya Tg(CAG-cre/Esr1*)5Amc/0
(B6.Cg-Kansl1em1Cya Tg(CAG-cre/Esr1*)5Amc)
|
abnormal autophagy
|
J:327464
|
abnormal mitophagy
|
J:327464
|
abnormal neuron mitochondrial morphology
|
J:327464
|
oxidative stress
|
J:327464
|
Kansl1em1Cya/Kansl1em1Cya Tg(CAG-cre/Esr1*)5Amc/0 Igs2tm1(CAG-mt-Keima)Fink/Igs2+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA * FVB/N)
|
abnormal mitophagy
|
J:327464
|
Kansl3em1(IMPC)J/Kansl3em1(IMPC)J
(C57BL/6NJ-Kansl3em1(IMPC)J/Mmjax)
|
abnormal epigenetic regulation of gene expression
|
J:350482
|
Kash5tm1b(KOMP)Wtsi/Kash5tm1b(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal chromosomal synapsis
|
J:201813
|
abnormal double-strand DNA break repair
|
J:201813
|
abnormal meiotic attachment of telomere to nuclear envelope
|
J:201813
|
abnormal oogenesis
|
J:201813
|
abnormal spermatocyte morphology
|
J:201813
|
arrest of male meiosis
|
J:201813
|
decreased male germ cell number
|
J:201813
|
increased testis apoptosis
|
J:201813
|
Kat2atm1Roth/Kat2atm1Roth Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6J)
|
decreased embryonic tissue cell apoptosis
|
J:121357
|
Kat2atm2Roth/Kat2atm2Roth
(involves: 129S7/SvEvBrd * C57BL/6J)
|
decreased fibroblast proliferation
|
J:121357
|
increased embryonic tissue cell apoptosis
|
J:121357
|
Kat5tm1Jwl/Kat5+ Tg(IghMyc)22Bri/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL * C57BL/6 * SJL)
|
abnormal DNA repair
|
J:125164
|
Kat6atm2.2Avo/Kat6atm2.2Avo
(either: (involves: 129 * C57BL/6) or (involves: 129 * BALB/c * FVB/N))
|
abnormal chromosome morphology
|
J:155755
|
Kat6bGt(pKC199)1Pgr/Kat6bGt(pKC199)1Pgr
(involves: 129S2/SvPas)
|
abnormal neuronal migration
|
J:178264
|
Kat7tm1.1Avo/Kat7tm1.1Avo Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * CBA)
|
cellular phenotype
|
J:170405
|
Kat7tm1.2Avo/Kat7tm1.2Avo
(involves: C57BL/6)
|
cellular phenotype
|
J:170405
|
increased embryonic tissue cell apoptosis
|
J:170405
|
Kat8tm1.1Avo/Kat8tm1.1Avo
(involves: BALB/cJ * C57BL/6)
|
abnormal chromosome morphology
|
J:139761
|
abnormal inner cell mass apoptosis
|
J:139761
|
absent inner cell mass proliferation
|
J:139761
|
decreased trophectoderm cell proliferation
|
J:139761
|
increased mitotic index
|
J:139761
|
Kat8tm1Thl/Kat8tm1Thl Tg(Gdf9-icre)5092Coo/0
(involves: 129S1/Sv * C57BL/6)
|
abnormal epigenetic regulation of gene expression
|
J:242000
|
abnormal female germ cell physiology
|
J:242000
|
abnormal oocyte morphology
|
J:242000
|
abnormal oogenesis
|
J:242000
|
decreased oocyte number
|
J:242000
|
increased female germ cell apoptosis
|
J:242000
|
oxidative stress
|
J:242000
|
Kat14Gt(OST388291)Lex/Kat14Gt(OST388291)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell cycle
|
J:145720
|
increased apoptosis
|
J:145720
|
increased embryonic neuroepithelium apoptosis
|
J:145720
|
Katna1tm1a(KOMP)Wtsi/Katna1+
(involves: C57BL/6J * C57BL/6N)
|
abnormal neuronal precursor proliferation
|
J:284578
|
decreased neuronal precursor proliferation
|
J:284578
|
Katnal11H/Katnal11H
(involves: C3H/HeH * C57BL/6J)
|
decreased elongated spermatid number
|
J:185195
|
decreased spermatid number
|
J:185195
|
oligozoospermia
|
J:185195
|
Katnal2em1Zhlu/Katnal2em1Zhlu
(C57BL/6-Katnal2em1Zhlu)
|
abnormal sperm head morphology
|
J:322392
|
asthenozoospermia
|
J:322392
|
oligozoospermia
|
J:322392
|
teratozoospermia
|
J:322392
|
Katnal2m1Anu/Katnal2m1Anu
(C57BL/6J-Katnal2m1Anu)
|
abnormal manchette disassembly
|
J:250115
|
abnormal manchette perinuclear ring morphology
|
J:250115
|
abnormal outer dense fiber morphology
|
J:250115
|
abnormal sperm axoneme morphology
|
J:250115
|
abnormal sperm flagellum morphology
|
J:250115
|
abnormal sperm head morphology
|
J:250115
|
abnormal sperm mitochondrial sheath morphology
|
J:250115
|
abnormal spermatid morphology
|
J:250115
|
absent sperm flagellum
|
J:250115
|
absent sperm mitochondrial sheath
|
J:250115
|
detached acrosome
|
J:250115
|
elongated manchette
|
J:250115
|
immotile sperm
|
J:250115
|
multinucleated giant male germ cells
|
J:250115
|
short sperm flagellum
|
J:250115
|
Katnal2m1Anu/Katnal2tm1a(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal elongated spermatid morphology
|
J:250115
|
multinucleated giant male germ cells
|
J:250115
|
Katnal2tm1a(EUCOMM)Wtsi/Katnal2tm1a(EUCOMM)Wtsi
(C57BL/6N-Katnal2tm1a(EUCOMM)Wtsi)
|
abnormal elongated spermatid morphology
|
J:250115
|
multinucleated giant male germ cells
|
J:250115
|
Katnal2tm1c(EUCOMM)Wtsi/Katnal2tm1c(EUCOMM)Wtsi Tg(Stra8-icre)1Reb/0
(involves: C57BL/6N * FVB/NJ)
|
abnormal elongated spermatid morphology
|
J:250115
|
abnormal sperm flagellum morphology
|
J:250115
|
elongated manchette
|
J:250115
|
multinucleated giant male germ cells
|
J:250115
|
Katnb1taily/Katnb1taily
(involves: C57BL/6 * CBA)
|
abnormal male meiosis
|
J:185194
|
abnormal manchette disassembly
|
J:185194
|
abnormal manchette morphology
|
J:185194
|
abnormal manchette perinuclear ring morphology
|
J:185194
|
abnormal meiotic spindle morphology
|
J:185194
|
abnormal outer dense fiber morphology
|
J:185194
|
abnormal sperm axoneme morphology
|
J:185194
|
abnormal sperm flagellum morphology
|
J:185194
|
absent sperm axonemal central pair
|
J:185194
|
asthenozoospermia
|
J:185194
|
decreased sperm progressive motility
|
J:185194
|
decreased spermatid number
|
J:185194
|
elongated manchette
|
J:185194
|
globozoospermia
|
J:185194
|
oligozoospermia
|
J:185194
|
Katnb1tm1a(EUCOMM)Hmgu/Katnb1tm1a(EUCOMM)Hmgu
(C57BL/6-Katnb1tm1a(EUCOMM)Hmgu)
|
abnormal cell cytoskeleton morphology
|
J:220901
|
abnormal cell morphology
|
J:220901
|
abnormal mitosis
|
J:220901
|
abnormal mitotic spindle morphology
|
J:220901
|
abnormal neuronal precursor proliferation
|
J:220901
|
abnormal primary cilium morphology
|
J:220901
|
aneuploidy
|
J:220901
|
binucleate
|
J:220901
|
decreased fibroblast proliferation
|
J:220901
|
increased brain apoptosis
|
J:220901
|
Kcna1tm1Tem/Kcna1tm1Tem
(C3Fe.129S7-Kcna1tm1Tem)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:206598
|
oxidative stress
|
J:206598
|
Kcna3tm1Gvd/Kcna3tm1Gvd
(involves: 129S1/Sv * C57BL/6)
|
increased skeletal muscle cell glucose uptake
|
J:88651
|
Kcna5tm1Hket/Kcna5tm1Hket
(involves: 129S6/SvEvTac * 129S7/SvEvBrd)
|
abnormal cell proliferation
|
J:116545
|
Kcng4tm1(KOMP)Vlcg/Kcng4tm1(KOMP)Vlcg
(C57BL/6N-Kcng4tm1(KOMP)Vlcg)
|
abnormal elongated spermatid morphology
|
J:302033
|
abnormal sperm head morphology
|
J:302033
|
abnormal sperm midpiece morphology
|
J:302033
|
asthenozoospermia
|
J:302033
|
decreased elongated spermatid number
|
J:302033
|
decreased sperm progressive motility
|
J:302033
|
necrospermia
|
J:302033
|
oligozoospermia
|
J:302033
|
short sperm flagellum
|
J:302033
|
small sperm head
|
J:302033
|
teratozoospermia
|
J:302033
|
Kcnh6em1Jkya/Kcnh6em1Jkya
(involves: C57BL/6N)
|
increased endoplasmic reticulum stress
|
J:271003
|
increased pancreatic islet cell apoptosis
|
J:271003
|
Kcnj6wv/Kcnj6+
(B6CBA Aw-J/A-Kcnj6wv)
|
abnormal male germ cell morphology
|
J:23163
|
abnormal sperm motility
|
J:23163
|
abnormal spermatid morphology
|
J:23163
|
oligozoospermia
|
J:23163
|
Kcnj6wv/Kcnj6+
(involves: C57BL/6J)
|
abnormal cell migration
|
J:16025
|
increased apoptosis
|
J:16025
|
Kcnj6wv/Kcnj6wv
(B6CBA Aw-J/A-Kcnj6wv)
|
abnormal male germ cell morphology
|
J:23163
|
abnormal sperm motility
|
J:23163
|
abnormal spermatid morphology
|
J:106298
|
globozoospermia
|
J:23163
|
oligozoospermia
|
J:23163
|
Kcnj6wv/Kcnj6wv
(involves: C57BL/6J)
|
abnormal cell migration
|
J:16025
|
increased apoptosis
|
J:16025
|
Kcnj6wv/Kcnj6wv
(involves: C57BL/6 * CBA/CaGnLe)
|
azoospermia
|
J:18348
|
increased apoptosis
|
J:46842
|
Kcnma1tm1Ruth/Kcnma1tm1Ruth
(involves: 129X1/SvJ)
|
increased apoptosis
|
J:92443
|
Kcnq1ot1tm1.1Ckan/Kcnq1ot1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * M. spretus)
|
abnormal DNA methylation
|
J:163857
|
abnormal imprinting
|
J:163857
|
Kcnq1ot1tm1.1Ckan/Kcnq1ot1tm1.1Ckan
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
cellular phenotype
|
J:163857
|
Kcnq1ot1tm1.1Mjh/Kcnq1ot1+
(involves: 129S4/SvJae * C57BL/6J * FVB/N)
|
maternal imprinting
|
J:79882
|
Kcnq1ot1tm1.1Mjh/Del(7Ins2-Tel)1Lef
(involves: 129 * C57BL/6 * ICR)
|
abnormal imprinting
|
J:130399
|
Kcnq1ot1tm1Tilg/Kcnq1ot1+
(involves: 129S1/Sv * C57BL/6 * M. spretus)
|
abnormal imprinting
|
J:108700
|
Kcnq1ot1tm2.1Ckan/Kcnq1ot1+ Meox2tm1(cre)Sor/Meox2+
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6 * SD7)
|
abnormal imprinting
|
J:185569
|
Kcnq1ot1tm2.1Ckan/Kcnq1ot1+ Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SD7)
|
abnormal DNA methylation
|
J:185569
|
abnormal imprinting
|
J:185569
|
Kcnq1ot1tm2Mjh/Kcnq1ot1+
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal imprinting
|
J:130529
|
Kcnq1ot1tm2Tilg/Kcnq1ot1+
(involves: 129S1/Sv * C57BL/6 * M. spretus)
|
abnormal imprinting
|
J:108700
|
Kcnq1ot1tm2Tilg/Kcnq1ot1+
(involves: 129S1/Sv * M. spretus)
|
abnormal imprinting
|
J:163857
|
Kcnq1ot1tm3Mjh/Kcnq1ot1+
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
genetic imprinting
|
J:130529
|
Kcnq1ot1tm3Tilg/Kcnq1ot1+
(involves: 129S1/Sv * C57BL/6 * M. spretus)
|
abnormal imprinting
|
J:108700
|
Kcnq1ot1tm4Tilg/Kcnq1ot1+
(involves: 129S1/Sv * C57BL/6 * M. spretus)
|
abnormal imprinting
|
J:108700
|
Kcnu1tm1.2Clin/Kcnu1tm1.2Clin
(B6.Cg-Kcnu1tm1.2Clin)
|
asthenozoospermia
|
J:171225
|
Kcnu1tm1Cmsa/Kcnu1tm1Cmsa
(Not Specified)
|
decreased sperm progressive motility
|
J:157522
|
Kcnv2tm1.2(KOMP)Wtsi/Kcnv2tm1.2(KOMP)Wtsi
(involves: 129S6/SvEvTac * C57BL/6N)
|
increased retina apoptosis
|
J:279816
|
Kctd13em1Djla/Kctd13em1Djla
(Not Specified)
|
asthenozoospermia
|
J:330265
|
decreased male germ cell number
|
J:330265
|
oligozoospermia
|
J:330265
|
Kctd19em1Fcw/Kctd19em1Fcw
(Not Specified)
|
abnormal male meiosis
|
J:338159
|
azoospermia
|
J:338159
|
increased male germ cell apoptosis
|
J:338159
|
Kctd19em1Osb/Kctd19em1Osb
(Not Specified)
|
abnormal male meiosis
|
J:306305
|
abnormal synaptonemal complex
|
J:306305
|
arrest of male meiosis
|
J:306305
|
azoospermia
|
J:306305
|
decreased round spermatid number
|
J:306305
|
increased primordial germ cell apoptosis
|
J:306305
|
Kdf1shd/Kdf1shd
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal keratinocyte differentiation
|
J:203995
|
increased keratinocyte proliferation
|
J:203995
|
Kdf1shd/Kdf1tm1a(EUCOMM)Wtsi
(involves: C3HeB/FeJ * C57BL/6J * C57BL/6N)
|
abnormal keratinocyte differentiation
|
J:203995
|
Kdf1tm1a(EUCOMM)Wtsi/Kdf1tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal keratinocyte differentiation
|
J:203995
|
Kdm1atm1.1Rsd/Kdm1atm1.1Rsd Tg(Pitx1-cre)7Rsd/0
(involves: BALB/c * C57BL/6)
|
abnormal cell cycle
|
J:121427
|
Kdm1atm1.2Tche/Kdm1atm1.2Tche
(involves: 129 * C57BL/6)
|
increased apoptosis
|
J:144527
|
Kdm1btm1.1Tche/Kdm1btm1.1Tche
(Not Specified)
|
maternal effect
|
J:152382
|
Kdm2atm1d(KOMP)Mtok/Kdm2atm1d(KOMP)Mtok
(involves: C57BL/6 * C57BL/6JJcl * C57BL/6N)
|
abnormal neuron proliferation
|
J:217589
|
impaired neuron differentiation
|
J:217589
|
increased neural crest cell apoptosis
|
J:217589
|
increased neuron apoptosis
|
J:217589
|
Kdm2btm1Nobu/Kdm2btm1Nobu
(either: (involves: 129S/SvEv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6J))
|
abnormal neuronal precursor proliferation
|
J:171291
|
increased embryonic neuroepithelium apoptosis
|
J:171291
|
increased head mesenchyme apoptosis
|
J:171291
|
oligozoospermia
|
J:171291
|
Kdm3aGt(YHA186)Byg/Kdm3aGt(YHA186)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal acrosome assembly
|
J:127121
|
abnormal sperm head morphology
|
J:127121
|
abnormal spermatid morphology
|
J:127121
|
asthenozoospermia
|
J:127121
|
decreased elongated spermatid number
|
J:127121
|
oligozoospermia
|
J:127121
|
Kdm3atm1Jxu/Kdm3atm1Jxu
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal spermatid morphology
|
J:159956
|
increased male germ cell apoptosis
|
J:159956
|
oligozoospermia
|
J:159956
|
Kdm3btm1Jxu/Kdm3btm1Jxu
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal oocyte morphology
|
J:286338
|
Kdm4btm1.1Okad/Kdm4btm1.1Okad
(involves: 129P2/OlaHsd)
|
decreased mammary gland epithelial cell proliferation
|
J:171678
|
Kdm4ctm1d(KOMP)Wtsi/Kdm4ctm1d(KOMP)Wtsi
(involves: BALB/cJ * C57BL/6N)
|
cellular phenotype
|
J:231987
|
Kdm4dtm1Zuk/Kdm4dtm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal male germ cell apoptosis
|
J:173703
|
abnormal spermatid morphology
|
J:173703
|
Kdm5atm1.1Kael/Kdm5a+ Rb1tm1Tyj/Rb1tm1Tyj
(involves: 129S2/SvPas * 129S6/SvEvTac * FVB/N)
|
increased fibroblast proliferation
|
J:175625
|
Kdm5atm1.1Kael/Kdm5atm1.1Kael
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL)
|
abnormal cell cycle
|
J:137185
|
Kdm5atm1.1Kael/Kdm5atm1.1Kael
(involves: 129S6/SvEvTac * FVB/N)
|
early cellular replicative senescence
|
J:175625
|
Kdm5atm1.1Kael/Kdm5atm1.1Kael Rb1tm1Tyj/Rb1tm1Tyj
(involves: 129S2/SvPas * 129S6/SvEvTac * FVB/N)
|
abnormal cell differentiation
|
J:175625
|
cellular phenotype
|
J:175625
|
Kdm5atm1Kael/Kdm5atm1Kael
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
early cellular replicative senescence
|
J:175625
|
Kdm5atm1Kael/Kdm5atm1Kael Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
early cellular replicative senescence
|
J:175625
|
Kdm6atm1.1Afst/Kdm6atm1.1Afst Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6NTac)
|
spontaneous chromosome breakage
|
J:196401
|
Kdm6btm1.1Cdcn/Kdm6btm1.1Cdcn
(involves: C57BL/6)
|
abnormal osteoblast differentiation
|
J:233350
|
decreased chondrocyte proliferation
|
J:233350
|
Kdm6btm1.1Iwam/Kdm6btm1.2Iwam Tg(Stra8-icre)1Reb/0
(involves: 129P2/OlaHsd * C57BL/6J * FVB/NJ)
|
abnormal spermatogonia morphology
|
J:206350
|
Kdm6btm1.1Rbo/Kdm6btm1.1Rbo H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S4/SvJae * C57BL/6J * CBA/J)
|
abnormal cell physiology
|
J:323190
|
Kdm6btm1.1Rfw/Kdm6btm1.1Rfw
(Not Specified)
|
increased cell proliferation
|
J:228713
|
Kdm8tm1Tasu/Kdm8tm1Tasu
(involves: 129S4/SvJae * C57BL/6)
|
decreased cell proliferation
|
J:181189
|
Kdrorv/Kdrorv
(involves: 129S1/Sv * C57BL/6 * FVB/NJ)
|
abnormal cranial neural crest cell migration
|
J:171522
|
Kdrtm1.1Jamb/Kdrtm1.1Jamb Tg(Pax6-cre,GFP)1Pgr/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N * ICR)
|
abnormal basement membrane morphology
|
J:154336
|
Khdc3tm1Dean/Khdc3tm1Dean
(involves: 129/Sv * C57BL/6)
|
maternal effect
|
J:148330
|
Khdrbs1tm1Rchd/Khdrbs1tm1Rchd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal osteoblast physiology
|
J:115775
|
Khdrbs2Tg(LRRK2*R1441G)135Cjli/Khdrbs2+
(FVB/N-Khdrbs2Tg(LRRK2*R1441G)135Cjli/J)
|
abnormal autophagy
|
J:194153
|
Kidins220tm1.2Fces/Kidins220tm1.2Fces
(involves: 129 * BALB/c * C57BL/6 * C57BL/6J)
|
abnormal neuron differentiation
|
J:203073
|
increased neuron apoptosis
|
J:203073
|
increased retina apoptosis
|
J:203073
|
Kif2atm1Noh/Kif2atm1Noh
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal axon extension
|
J:107737
|
delayed neuronal migration
|
J:107737
|
Kif3atm1Gsn/Kif3atm1Gsn
(involves: 129S1/Sv * 129X1/SvJ)
|
absent embryonic cilia
|
J:54575
|
Kif3atm1Gsn/Kif3atm2Gsn Tg(Cdh16-cre)91Igr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * ICR)
|
absent kidney epithelial cell primary cilium
|
J:83293
|
increased kidney apoptosis
|
J:83293
|
Kif3atm1Noh/Kif3atm1Noh
(involves: 129S4/SvJae * C57BL/6J)
|
absent embryonic cilia
|
J:55332
|
absent nodal flow
|
J:55332
|
Kif3atm2Gsn/Kif3atm2Gsn H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J)
|
increased cranial neural crest cell proliferation
|
J:158523
|
Kif3atm2Gsn/Kif3atm2Gsn Tg(Col2a1-cre)1Bhr/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal actin cytoskeleton morphology
|
J:121342
|
Kif3atm2Gsn/Kif3atm2Gsn Tg(NEUROG3-cre)1Herr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal manchette disassembly
|
J:210780
|
abnormal manchette morphology
|
J:210780
|
abnormal manchette perinuclear ring morphology
|
J:210780
|
abnormal outer dense fiber morphology
|
J:210780
|
abnormal sperm axoneme morphology
|
J:210780
|
abnormal sperm fibrous sheath morphology
|
J:210780
|
abnormal sperm flagellum morphology
|
J:210780
|
abnormal sperm head morphology
|
J:210780
|
abnormal sperm nucleus morphology
|
J:210780
|
abnormal spermatid morphology
|
J:210780
|
disorganized sperm mitochondrial sheath
|
J:210780
|
ectopic manchette
|
J:210780
|
elongated manchette
|
J:210780
|
oligozoospermia
|
J:210780
|
Kif3btm1Noh/Kif3btm1Noh
(involves: 129S4/SvJae * C57BL/6J)
|
absent embryonic cilia
|
J:51419
|
Kif5atm1Gsn/Kif5atm1Gsn
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal vesicle-mediated transport
|
J:170887
|
Kif5btm1Njen/Kif5btm1Njen
(involves: 129S1/Sv)
|
abnormal vesicle-mediated transport
|
J:170887
|
Kif5btm1Noh/Kif5btm1Noh
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal lysosome morphology
|
J:48447
|
abnormal mitochondrial morphology
|
J:48447
|
Kif5ctm2Gsn/Kif5ctm2Gsn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal vesicle-mediated transport
|
J:170887
|
Kif6em1Rgray/Kif6em1Rgray
(involves: C57BL/6J)
|
abnormal brain ependyma motile cilium morphology
|
J:269442
|
Kif7tm1.2Hui/Kif7tm1.2Hui
(involves: 129S6/SvEvTac * CD-1)
|
abnormal neuron differentiation
|
J:152259
|
Kif7tm1.2Hui/Kif7tm1.2Hui Smotm1Amc/Smotm1Amc
(involves: 129S6/SvEvTac * 129X1/SvJ * CD-1)
|
abnormal neuron differentiation
|
J:152259
|
Kif9em1Osb/Kif9em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
asthenozoospermia
|
J:303071
|
decreased sperm progressive motility
|
J:303071
|
Kif9em2Osb/Kif9em2Osb
(involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2)
|
asthenozoospermia
|
J:303071
|
decreased sperm progressive motility
|
J:303071
|
Kif13bGt(AF0005)Wtsi/Kif13bGt(AF0005)Wtsi
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal fibroblast physiology
|
J:282570
|
Kif14lag/Kif14lag
(B6.D2(129X1)-Kif14lag)
|
abnormal cerebellar granule cell migration
|
J:195809
|
decreased cell proliferation
|
J:195809
|
increased apoptosis
|
J:195809
|
Kif18agcd2/Kif18agcd2
(involves: 129S1/Sv * C57BL/6)
|
decreased germ cell number
|
J:111998,
J:86161
|
decreased male germ cell number
|
J:111998
|
decreased oocyte number
|
J:111998
|
Kif18agcd2/Kif18agcd2
(CAST.129S1(B6)-Kif18agcd2/JcsJ)
|
decreased germ cell number
|
J:111998
|
decreased male germ cell number
|
J:111998
|
decreased oocyte number
|
J:111998
|
decreased primordial germ cell number
|
J:111998
|
Kif18agcd2/Kif18agcd2
(CAST.129S1(B6)-Kif18agcd2/JcsMmjax)
|
abnormal cell cycle checkpoint function
|
J:222418
|
abnormal cell physiology
|
J:222418
|
abnormal mitosis
|
J:222418
|
abnormal mitotic spindle assembly checkpoint
|
J:222418
|
abnormal mitotic spindle morphology
|
J:222418
|
abnormal spermatogonia morphology
|
J:222418
|
decreased fibroblast proliferation
|
J:222418
|
decreased germ cell number
|
J:222418
|
increased apoptosis
|
J:222418
|
Kif18atm1.1Lgr/Kif18atm1.1Lgr Tg(Zp3-cre)93Knw/0
(Not Specified)
|
abnormal female meiosis
|
J:352185
|
abnormal meiotic configurations
|
J:352185
|
meiotic nondisjunction
|
J:352185
|
Kif18atm1Zgwg/Kif18atm1Zgwg
(either: 129-Kif18atm1Zgwg or (involves: 129 * C57BL/6J))
|
abnormal mitosis
|
J:211103
|
arrest of male meiosis
|
J:211103
|
decreased cell proliferation
|
J:211103
|
increased male germ cell apoptosis
|
J:211103
|
Kif19atm1Noh/Kif19a+
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal oviduct epithelium motile cilium morphology
|
J:191072
|
Kif19atm1Noh/Kif19atm1Noh
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal oviduct epithelium motile cilium morphology
|
J:191072
|
abnormal respiratory motile cilium morphology
|
J:191072
|
increased brain ependyma motile cilium length
|
J:191072
|
Kif20bmagoo/Kif20bmagoo
(involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal mitosis
|
J:205043
|
abnormal neuronal precursor proliferation
|
J:205043
|
increased neuron apoptosis
|
J:205043
|
Kif20bmagoo/Kif20bmagoo
(involves: BALB/c * C57BL/6)
|
abnormal axon extension
|
J:242310
|
abnormal microtubule cytoskeleton morphology
|
J:242310
|
Kif20bmagoo/Kif20bmagoo Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw
(involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal axon extension
|
J:168258
|
Kif21atm1.1Ece/Kif21atm1.1Ece Tg(Isl1-EGFP*)1Slp/0
(involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6)
|
abnormal axon extension
|
J:213171
|
increased neuron apoptosis
|
J:213171
|
Kif22tm1.1Tya/Kif22tm1.1Tya
(involves: 129P2/OlaHsd * C57BL/6J * C57BL/6)
|
abnormal chromosome morphology
|
J:145315
|
Kif26atm1.1Noh/Kif26atm1.1Noh
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J)
|
abnormal axon extension
|
J:154859
|
abnormal neuronal precursor proliferation
|
J:154859
|
Kif27Gt(OST441915)Lex/Kif27Gt(OST441915)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
cellular phenotype
|
J:185566
|
Kirrel1Gt(VICTR20)20Lex/Kirrel1Gt(VICTR20)20Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
increased mesangial cell number
|
J:74230
|
Kiss1tm1Coll/Kiss1tm1Coll
(involves: 129S/SvEv * 129S6/SvEvTac)
|
azoospermia
|
J:122381
|
retention of the adrenal gland x-zone
|
J:122381
|
Kiss1tm1Rla/Kiss1tm1Rla
(involves: 129S1/SvImJ)
|
decreased spermatid number
|
J:126704
|
Kiss1rtm1.1Aeh/Kiss1rtm1.1Aeh Tg(Gnrh1-cre)1Dlc/0
(involves: C57BL/6 * CBA)
|
azoospermia
|
J:206044
|
Kiss1rtm1.1Hjn/Kiss1rtm1.1Hjn Tg(Gnrh1-cre)35Awo/0
(involves: 129 * C57BL/6 * CD-1)
|
abnormal oogenesis
|
J:212351
|
oligozoospermia
|
J:212351
|
Kiss1rtm1.1Lex/Kiss1rtm1.1Lex
(involves: 129S4/SvJae)
|
azoospermia
|
J:181650
|
Kiss1rtm1Coll/Kiss1rtm1Coll
(involves: 129S6/SvEvTac)
|
arrest of male meiosis
|
J:96442
|
azoospermia
|
J:96442
|
decreased spermatid number
|
J:96442
|
retention of the adrenal gland x-zone
|
J:96442
|
Kiss1rtm1Rla/Kiss1rtm1Rla
(involves: 129S1/SvImJ)
|
decreased spermatid number
|
J:126704
|
Kittm1.1Bsm/Kittm1.1Bsm
(involves: 129S1/Sv * BALB/c * C57BL/6J * FVB/N)
|
decreased male germ cell number
|
J:61141
|
Kittm1Alf/Kit+
(involves: 129S2/SvPas)
|
abnormal male germ cell morphology
|
J:103157
|
abnormal melanoblast migration
|
J:36230
|
abnormal oocyte morphology
|
J:67923
|
asthenozoospermia
|
J:103157
|
oligozoospermia
|
J:103157
|
Kittm1Alf/Kittm1Alf
(involves: 129S2/SvPas)
|
abnormal female germ cell morphology
|
J:36230
|
abnormal melanoblast migration
|
J:36230
|
abnormal primordial germ cell migration
|
J:36230
|
Kittm1Bpr/Kittm1Bpr
(either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6))
|
absent oocytes
|
J:100778
|
azoospermia
|
J:100778
|
Kittm1Hntr/Kittm1Hntr
(either: (involves: 129/Sv * C57BL/6 * DBA/2) or (involves: 129S1))
|
abnormal spermatogonia proliferation
|
J:60192
|
Kittm2Bsm/Kit+
(involves: 129X1/SvJ * C57BL/6J)
|
increased mast cell degranulation
|
J:83616
|
KitW-e/KitW-e
(involves: 101 * C3H)
|
abnormal primordial germ cell migration
|
J:16216
|
abnormal primordial germ cell morphology
|
J:16216
|
decreased primordial germ cell proliferation
|
J:16216
|
KitW-sh/KitW-sh
(involves: 101/H * C3H/HeH)
|
decreased mast cell degranulation
|
J:157470
|
KitW/KitW-v
(involves: C57BL)
|
azoospermia
|
J:4972
|
KitlSl-5R/KitlSl-5R
(C3H-KitlSl-5R)
|
decreased primordial germ cell number
|
J:115437
|
KitlSl-17H/Kitl+
(C3H/HeH-KitlSl-17H)
|
decreased primordial germ cell number
|
J:2880
|
KitlSl-17H/KitlSl-17H
(C3H/HeH-KitlSl-17H)
|
decreased male germ cell number
|
J:2880
|
decreased oocyte number
|
J:2880
|
decreased primordial germ cell number
|
J:2880,
J:115437
|
KitlSl-20J/KitlSl-20J
(C57BL/6J-KitlSl-20J/J)
|
absent primordial germ cells
|
J:86436
|
KitlSl-22R/KitlSl-22R
(C3H-KitlSl-22R)
|
decreased primordial germ cell number
|
J:115437
|
KitlSl-28R/KitlSl-28R
(C3.101Rl-KitlSl-28R)
|
decreased primordial germ cell number
|
J:115437
|
KitlSl-30R/KitlSl-30R
(C3.101Rl-KitlSl-30R)
|
decreased primordial germ cell number
|
J:115437
|
KitlSl-31R/KitlSl-31R
(C3H-KitlSl-31R)
|
decreased primordial germ cell number
|
J:115437
|
KitlSl-36R/KitlSl-36R
(C3H-KitlSl-36R)
|
abnormal primordial germ cell migration
|
J:115437
|
decreased primordial germ cell number
|
J:115437
|
decreased primordial germ cell proliferation
|
J:115437
|
KitlSl-39R/KitlSl-39R
(C3.B10Rl-KitlSl-39R)
|
abnormal primordial germ cell migration
|
J:115437
|
abnormal primordial germ cell morphology
|
J:115437
|
decreased primordial germ cell number
|
J:115437
|
decreased primordial germ cell proliferation
|
J:115437
|
increased primordial germ cell apoptosis
|
J:115437
|
KitlSl-42R/KitlSl-42R
(C3.101Rl-KitlSl-42R)
|
decreased primordial germ cell number
|
J:115437
|
KitlSl-con/Kitl+
(either: (involves: C3H/HeJ) or (involves: C3H/HeN))
|
decreased oocyte number
|
J:23593
|
KitlSl-con/KitlSl-con
(either: (involves: C3H/HeJ) or (involves: C3H/HeN))
|
decreased oocyte number
|
J:23593
|
KitlSl-d/KitlSl-d
(C3.D2-KitlSl-d)
|
abnormal primordial germ cell migration
|
J:115437
|
abnormal primordial germ cell morphology
|
J:115437
|
decreased primordial germ cell number
|
J:115437
|
decreased primordial germ cell proliferation
|
J:115437
|
increased primordial germ cell apoptosis
|
J:115437
|
KitlSl-gb/KitlSl-gb
(C3.Cg-KitlSl-gb)
|
abnormal primordial germ cell migration
|
J:115437
|
abnormal primordial germ cell morphology
|
J:115437
|
abnormal primordial germ cell proliferation
|
J:115437
|
absent primordial germ cells
|
J:115437
|
decreased primordial germ cell number
|
J:115437
|
increased primordial germ cell apoptosis
|
J:115437
|
KitlSl-J/KitlSl-J
(C3HeB/FeHu-KitlSl-J)
|
absent germ cells
|
J:145144
|
KitlSl-pan/Kitl+
(either: (involves: C3H/HeJ * C57BL/6J) or (involves: C3H/HeN * C57BL/6J))
|
decreased primordial germ cell number
|
J:23593
|
KitlSl-pan/KitlSl-pan
(involves: C3H)
|
decreased male germ cell number
|
J:4746
|
decreased oocyte number
|
J:4746
|
decreased primordial germ cell number
|
J:4746
|
KitlSl-pan/KitlSl-pan
(either: (involves: C3H/HeJ * C57BL/6J) or (involves: C3H/HeN * C57BL/6J))
|
decreased oocyte number
|
J:23593
|
decreased primordial germ cell number
|
J:23593
|
KitlSl/KitlSl-d
(involves: C57BL/6 * WC)
|
decreased primordial germ cell number
|
J:5547
|
KitlSl/KitlSl-d
((WC/ReJ KitlSl x B6.D2-KitlSl-d/J)F1-KitlSl/KitlSl-d/J)
|
abnormal osteoblast physiology
|
J:111273
|
Kitltm2.1Pbes/KitlSl
(involves: 129S1/Sv * C3H * C57BL/6J * FVB/N)
|
azoospermia
|
J:157170
|
Kitltm2.1Pbes/Kitltm2.1Pbes
(involves: 129S1/Sv * C57BL/6J * FVB/N)
|
decreased cell proliferation
|
J:157170
|
Kitltm3.1Pbes/Kitltm3.1Pbes
(involves: 129S1/Sv * C57BL/6J * FVB/N)
|
azoospermia
|
J:157170
|
Klkl/Klkl
(either: C.Cg-Klkl or (involves: C3H/HeJ * C57BL/6J))
|
arrest of male meiosis
|
J:44109
|
azoospermia
|
J:44109
|
Klkl/Klkl
(involves: C3H/HeJ * C57BL/6J)
|
oxidative stress
|
J:81240
|
Klkl/Klkl
(involves: C3H/J * C57BL/6J)
|
abnormal osteoblast physiology
|
J:56666
|
Klc1tm1Gsn/Klc1tm1Gsn
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal vesicle-mediated transport
|
J:170887
|
Klc2em1Jgao/Klc2em1Jgao
(involves: C57BL/6J)
|
abnormal mitochondrial morphology
|
J:345577
|
Klf3tm1Merc/Klf3tm1Merc
(FVB.129-Klf3tm1Merc)
|
abnormal cell differentiation
|
J:137267
|
Klf4tm1.1Khk/Klf4tm1.1Khk
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal colon goblet cell morphology
|
J:76493
|
Klf4tm1Khk/Klf4tm1Khk Tg(ED-L2-cre)267Jkat/0
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:161868
|
Klf4tm1Khk/Klf4tm1Khk Tg(Klf4-cre/ERT)1Wai/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal intestinal goblet cell morphology
|
J:188101
|
increased keratinocyte adhesion
|
J:189337
|
increased keratinocyte migration
|
J:189337
|
increased keratinocyte proliferation
|
J:187932,
J:189337
|
Klf5Gt(XB751)Byg/Klf5Gt(XB751)Byg
(B6.129P2-Klf5Gt(XB751)Byg)
|
decreased inner cell mass proliferation
|
J:168150
|
decreased trophectoderm cell proliferation
|
J:168150
|
Klf5tm1.1Jwel/Klf5tm1.1Jwel
(Not Specified)
|
decreased inner cell mass proliferation
|
J:168150
|
decreased trophectoderm cell proliferation
|
J:168150
|
Klf5tm1Jaw/Klf5tm1Jaw Tg(Pax6-cre,GFP)1Pgr/0
(involves: FVB)
|
increased cell proliferation
|
J:175263
|
Klf5tm2.1Rng/Klf5tm2.1Rng Tg(Postn-cre)1Sjc/0
(involves: C57BL/6)
|
cardiac interstitial fibrosis
|
J:156696
|
Klf6tm1Fdmn/Klf6tm1Fdmn
(involves: C57BL/6)
|
decreased cell proliferation
|
J:122926
|
Klf7tm1Rmz/Klf7tm1Rmz
(involves: 129/Sv * C57BL/6)
|
abnormal axon extension
|
J:99181
|
abnormal axon guidance
|
J:99181
|
Klf10tm1Wkle/Klf10tm1Wkle
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased keratinocyte apoptosis
|
J:182595
|
increased keratinocyte proliferation
|
J:182595
|
Klf13tm1Kren/Klf13tm1Kren
(B6.129-Klf13tm1Kren)
|
decreased splenocyte apoptosis
|
J:145839
|
decreased thymocyte apoptosis
|
J:145839
|
Klf14em1Cgw/Klf14em1Cgw
(C57BL/6J-Klf14em1Cgw)
|
abnormal centrosome morphology
|
J:227200
|
abnormal mitosis
|
J:227200
|
aneuploidy
|
J:227200
|
chromosomal instability
|
J:227200
|
polyploidy
|
J:227200
|
Klhl10tm1Zuk/Klhl10+
(chimera involves: 129S7/SvEvBrd * C57BL/6J)
|
decreased germ cell number
|
J:89621
|
Klhl31em1Eno/Klhl31em1Eno
(involves: C57BL/6)
|
increased mitochondrial number
|
J:247651
|
Klhl40tm1.1Itl/Klhl40tm1.1Itl
(involves: 129S6/SvEvTac * C57BL/6N)
|
increased skeletal muscle cell apoptosis
|
J:227534
|
Kmt2atm1.1Erns/Kmt2atm1.1Erns Tg(CAG-Bgeo/GFP)21Lbe/0
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:147104
|
Kmt2atm1.1Erns/Kmt2atm1.1Erns Tg(GFAP-cre)25Mes/0
(involves: 129S2/SvPas * FVB/N)
|
abnormal neuron differentiation
|
J:147104
|
abnormal neuronal precursor cell migration
|
J:147104
|
Kmt2atm1.1Jjdh/Kmt2atm1.1Jjdh
(involves: 129X1/SvJ)
|
decreased fibroblast proliferation
|
J:112159
|
Kmt2atm1.1Jjdh/Kmt2atm1.1Jjdh Kmt2btm1Jjdh/Kmt2btm1Jjdh
(involves: 129X1/SvJ)
|
decreased fibroblast proliferation
|
J:112159
|
Kmt2atm1.1Mlc/Kmt2atm1.1Mlc
(involves: 129P2/OlaHsd * C57BL/6)
|
early cellular replicative senescence
|
J:183048
|
Kmt2atm1.1Mlc/Kmt2atm1.1Mlc Trp53tm1Brd/Trp53tm1Brd
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6)
|
cellular phenotype
|
J:183048
|
Kmt2atm1Sjk/Kmt2atm1Sjk
(involves: 129S2/SvPas * CD-1)
|
abnormal myoblast differentiation
|
J:201612
|
Kmt2btm1.2Afst/Kmt2btm1.2Afst
(involves: 129P2/OlaHsd * BALB/c * C57BL/6 * SJL)
|
increased apoptosis
|
J:107403
|
Kmt2btm1Afst/Kmt2btm1.1Afst Amhr2tm3(cre)Bhr/Amhr2+
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6)
|
abnormal DNA methylation
|
J:166778
|
Kmt2btm1Afst/Kmt2btm1.1Afst Tg(Gdf9-icre)5092Coo/0
(involves: 129 * 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:166778
|
abnormal DNA methylation
|
J:166778
|
abnormal female meiosis I arrest
|
J:166778
|
abnormal imprinting
|
J:166778
|
Kmt2btm1Afst/Kmt2btm1.1Afst Tg(Zp3-cre)3Mrt/0
(involves: 129 * 129P2/OlaHsd * C57BL/6 * FVB/N)
|
abnormal DNA methylation
|
J:166778
|
Kmt2btm1Afst/Kmt2btm1Afst
(involves: 129P2/OlaHsd * C57BL/6)
|
increased apoptosis
|
J:107403
|
Kmt2btm1Jjdh/Kmt2btm1Jjdh
(Not Specified)
|
cellular phenotype
|
J:112159
|
Kmt2btm2.1Afst/Kmt2btm2.1Afst
(involves: 129 * C57BL/6)
|
abnormal DNA methylation
|
J:166778
|
Kmt2ctm1.1Jwle/Kmt2ctm1.1Jwle
(involves: 129S4/SvJae * 129X1/SvJ)
|
decreased cell proliferation
|
J:116064
|
Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:228913
|
Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig Myf5tm3(cre)Sor/Myf5+
(involves: 129S4/SvJaeSor * C57BL/6J)
|
abnormal brown fat cell differentiation
|
J:207891
|
Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig Tg(Nkx2-1-cre)2Sand/0
(involves: C57BL/6)
|
impaired neuron differentiation
|
J:301083
|
Kmt2dtm1.1Kaig/Kmt2dtm1.1Kaig Tg(Tnnt2-cre)5Blh/0
(B6.Cg-Kmt2dtm1.1Kaig Tg(Tnnt2-cre)5Blh)
|
decreased fetal cardiomyocyte proliferation
|
J:229890
|
Kmt2etm1.1Hjf/Kmt2etm1.1Hjf
(B6.129P2-Kmtetm1.1Hjf)
|
globozoospermia
|
J:145579
|
Kmt2etm1Apa/Kmt2etm1Apa
(129S6/SvEvTac-Kmt2etm1Apa)
|
abnormal acrosome morphology
|
J:181000
|
abnormal granulocyte differentiation
|
J:145445
|
abnormal neutrophil differentiation
|
J:145445
|
abnormal sperm head morphology
|
J:181000
|
abnormal sperm nucleus morphology
|
J:181000
|
asthenozoospermia
|
J:181000
|
decreased sperm progressive motility
|
J:181000
|
detached acrosome
|
J:181000
|
Kmt5atm1.1Dare/Kmt5atm1.2Dare Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S1/Sv * C57BL/6 * CBA * SJL)
|
abnormal cell cycle checkpoint function
|
J:147765
|
abnormal cell physiology
|
J:147765
|
abnormal DNA repair
|
J:147765
|
decreased DNA replication
|
J:147765
|
increased apoptosis
|
J:147765
|
Kmt5btm1.1Jnw/Kmt5btm1.1Jnw Kmt5ctm1.1Jnw/Kmt5ctm1.1Jnw
(involves: 129 * C57BL/6J)
|
abnormal cell cycle
|
J:139510
|
abnormal DNA repair
|
J:139510
|
decreased fibroblast proliferation
|
J:139510
|
early cellular replicative senescence
|
J:139510
|
increased cellular sensitivity to hydroxyurea
|
J:139510
|
increased cellular sensitivity to ultraviolet irradiation
|
J:139510
|
Knk/Knk
(involves: C57BL/6J * FVB/N)
|
abnormal basement membrane morphology
|
J:154368
|
Knl1tm1c(EUCOMM)Hmgu/Knl1tm1c(EUCOMM)Hmgu Tg(GFAP-cre)25Mes/0
(involves: 129S4/SvJaeSor * C57BL/6N * FVB/N)
|
abnormal double-strand DNA break repair
|
J:278483
|
abnormal mitotic cytokinesis
|
J:278483
|
increased apoptosis
|
J:278483
|
premature neuronal precursor differentiation
|
J:278483
|
Knl1tm1c(EUCOMM)Hmgu/Knl1tm1c(EUCOMM)Hmgu Trp53tm1Brn/Trp53tm1Brn Tg(GFAP-cre)25Mes/0
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N * FVB/N)
|
aneuploidy
|
J:278483
|
increased apoptosis
|
J:278483
|
Knstrntm1d(KOMP)Wtsi/Knstrntm1d(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal spermatogonia proliferation
|
J:232595
|
decreased male germ cell number
|
J:232595
|
increased testis apoptosis
|
J:232595
|
oligozoospermia
|
J:232595
|
Kpna2em1Alfon/Kpna2em1Alfon
(involves: C57BL/6 * CBA)
|
abnormal sperm flagellum morphology
|
J:338393
|
abnormal sperm head morphology
|
J:338393
|
abnormal sperm midpiece morphology
|
J:338393
|
asthenozoospermia
|
J:338393
|
decreased sperm progressive motility
|
J:338393
|
teratozoospermia
|
J:338393
|
Kpna4tm1Maoka/Kpna4tm1Maoka
(B6.Cg-Kpna4tm1Maoka)
|
abnormal sperm axoneme morphology
|
J:303081
|
abnormal sperm flagellum morphology
|
J:303081
|
abnormal sperm head morphology
|
J:303081
|
decreased sperm progressive motility
|
J:303081
|
Kpna6Gt(AJ0609)Wtsi/Kpna6Gt(AJ0609)Wtsi
(B6N.129P2-Kpna6Gt(AJ0609)Wtsi)
|
abnormal spermatocyte morphology
|
J:311959
|
decreased round spermatid number
|
J:311959
|
oligozoospermia
|
J:311959
|
Kpna6Gt(AJ0609)Wtsi/Kpna6tm1Bdr
(B6N.Cg-Kpna6Gt(AJ0609)Wtsi Kpna6tm1Bdr)
|
oligozoospermia
|
J:311959
|
Kpna6tm1Bdr/Kpna6tm1Bdr
(involves: C57BL/6)
|
maternal effect
|
J:171441
|
Kpna6tm1Bdr/Kpna6tm1Bdr
(B6N.Cg-Kpna6tm1Bdr)
|
abnormal sperm head morphology
|
J:311959
|
abnormal spermatocyte morphology
|
J:311959
|
decreased male germ cell number
|
J:311959
|
decreased round spermatid number
|
J:311959
|
increased male germ cell apoptosis
|
J:311959
|
multinucleated giant male germ cells
|
J:311959
|
oligozoospermia
|
J:311959
|
Kpna7tm1.1Sgao/Kpna7tm1.1Sgao
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell cycle
|
J:244973
|
abnormal female germ cell physiology
|
J:244973
|
Krastm1.1Hbji/Krastm1.1Hbji Trp53tm5Tyj/Trp53tm5Tyj
(involves: 129S4/SvJae)
|
increased fibroblast proliferation
|
J:220921
|
Krastm1Bbd/Kras+ Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd Raf1tm2Bacc/Raf1tm2Bacc
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:172200
|
Krastm1Bbd/Kras+ Tg(CMV-cre)1Cgn/?
(involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6)
|
abnormal cell proliferation
|
J:86101
|
Krastm1Bbd/Kras+ Tg(CMV-cre/ERT)1Ipc/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal fibroblast proliferation
|
J:86101
|
Krastm1Bbd/Krastm2Bbd Polr2atm1(cre/ERT2)Bbd/Polr2atm1(cre/ERT2)Bbd
(involves: 129S1/Sv * 129X1/SvJ)
|
increased cell proliferation
|
J:161780
|
Krastm1Mok/Krastm1Mok
(involves: 129S/SvEv * C57BL/6J)
|
abnormal fetal cardiomyocyte proliferation
|
J:42943
|
increased neuron apoptosis
|
J:42943
|
Krastm1Tyj/Kras+ Nrastm1Rak/Nrastm1Rak
(involves: 129/Sv * C57BL/6)
|
increased apoptosis
|
J:43433
|
increased embryonic tissue cell apoptosis
|
J:43433
|
Krastm1Tyj/Krastm1Tyj
(involves: 129S2/SvPas)
|
increased apoptosis
|
J:43433
|
Krastm4.1Bbd/Krastm4.1Bbd
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * FVB/N)
|
cellular necrosis
|
J:223433
|
increased cell proliferation
|
J:223433
|
Krastm4.1Tyj/Kras+
(Not Specified)
|
increased embryonic neuroepithelium apoptosis
|
J:89333
|
Krastm4Tyj/Kras+ Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129S4/SvJae)
|
abnormal colon goblet cell morphology
|
J:132357
|
Krastm4Tyj/Kras+ Krt19tm1(cre/ERT)Ggu/Krt19+
(involves: 129S4/SvJae * 129S6/SvEvTac)
|
increased cell proliferation
|
J:172048
|
Krastm4Tyj/Kras+ Map2k7tm1.1Twad/Map2k7tm1.2Twad
(B6.Cg-Krastm4Tyj Map2k7tm1.1Twad/Map2k7tm1.2Twad)
|
abnormal DNA repair
|
J:170904
|
Krastm4Tyj/Kras+ Meox2tm1(cre)Sor/Meox2+
(involves: 129S4/SvJae * 129S4/SvJaeSor)
|
increased hepatocyte apoptosis
|
J:119477
|
Krastm4Tyj/Kras+ Tg(Fabp1-cre)1Jig/0
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal intestinal goblet cell morphology
|
J:132357
|
Krastm4Tyj/Kras+ Tg(Mx1-cre)1Cgn/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
increased splenocyte proliferation
|
J:87429
|
Krastm4Tyj/Kras+ Tg(Prm-cre)58Og/0
(involves: 129S4/SvJae)
|
increased embryonic tissue cell apoptosis
|
J:119477
|
Krastm4Tyj/Kras+ Trp53tm2Tyj/Trp53+ Tg(Pdx1-cre)6Tuv/0
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
chromosomal instability
|
J:98936
|
Krastm4Tyj/Kras+ Trp53tm3Glo/Trp53+ Tg(KRT5-cre/PGR)1Der/?
(involves: 129/Sv * C57BL/6 * FVB * ICR)
|
abnormal centrosome morphology
|
J:124222
|
Krastm4Tyj/Krastm4Tyj
(B6.129S4-Krastm4Tyj)
|
increased cell proliferation
|
J:187371
|
Krt2tm1a(KOMP)Wtsi/Krt2tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal keratinocyte differentiation
|
J:214772
|
increased keratinocyte proliferation
|
J:214772
|
Krt7tm1Whim/Krt7tm1Whim
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cell proliferation
|
J:196575
|
Krt9tm1(KOMP)Vlcg/Krt9tm1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
increased keratinocyte proliferation
|
J:206051
|
Krt14tm1(Krt10)Pko/Krt14tm1(Krt10)Pko
(B6.Cg-Krt14tm1(Krt10)Pko)
|
abnormal keratinocyte apoptosis
|
J:117347
|
Krt16tm1(KOMP)Vlcg/Krt16tm1(KOMP)Vlcg
(C57BL/6-Krt16tm1(KOMP)Vlcg)
|
increased cell proliferation
|
J:184621
|
Krt17em1Cou/Krt17em1Cou
(C57BL/6-Krt17em1Cou)
|
abnormal cell nucleus morphology
|
J:331728
|
Krt17tm1Cou/Krt17tm1Cou
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
increased hair follicle apoptosis
|
J:82089
|
Krt18tm1Tmm/Krt18+
(involves: 129P2/OlaHsd)
|
chromosomal instability
|
J:309021
|
Krt18tm1Tmm/Krt18tm1Tmm
(involves: 129P2/OlaHsd)
|
chromosomal instability
|
J:309021
|
increased hepatocyte apoptosis
|
J:309021
|
Krt19tm1Alki/Krt19+
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:125621
|
abnormal spermatid morphology
|
J:125621
|
coiled sperm flagellum
|
J:125621
|
ectopic manchette
|
J:125621
|
short sperm flagellum
|
J:125621
|
thick sperm flagellum
|
J:125621
|
Krt19tm1Alki/Krt19tm1Alki
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:125621
|
abnormal spermatid morphology
|
J:125621
|
coiled sperm flagellum
|
J:125621
|
ectopic manchette
|
J:125621
|
short sperm flagellum
|
J:125621
|
thick sperm flagellum
|
J:125621
|
Ksr1tm1Kole/Ksr1tm1Kole
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell physiology
|
J:84644
|
decreased cell proliferation
|
J:84644
|
Ksr1tm1Shaw/Ksr1tm1Shaw
(Not Specified)
|
decreased T cell proliferation
|
J:75739
|
Ksr1tm1Shaw/Ksr1tm1Shaw
(involves: DBA/1LacJ)
|
abnormal cell differentiation
|
J:100406
|
Ksr1tm1Shaw/Ksr1tm1Shaw Tg(DO11.10)10Dlo/0
(involves: BALB/c * C3H * C57BL/6)
|
decreased T cell proliferation
|
J:75739
|
Kxd1tm1Wli/Kxd1tm1Wli
(involves: 129 * C57BL/6J)
|
cellular phenotype
|
J:238623
|
Kynuem1Dunw/Kynuem1Dunw
(involves: C57BL/6N)
|
maternal effect
|
J:272339
|
L1camtm1.1Pfm/Y
(Not Specified)
|
abnormal axon guidance
|
J:131051
|
L1camtm1.1Pfm/L1camtm1.1Pfm
(Not Specified)
|
abnormal axon guidance
|
J:131051
|
L1camtm1Sor/Y
(either: 129S7/SvEvBrd-L1camtm1Sor or (129S7/SvEvBrd * C57BL/6J)F1)
|
abnormal axon guidance
|
J:45013
|
L1camtm1Sor/Y
(involves: 129S7/SvEvBrd)
|
abnormal axon extension
|
J:47995
|
L3mbtl1tm1.1Haho/L3mbtl1tm1.1Haho
(involves: 129S4/SvJae * C57BL/6)
|
cellular phenotype
|
J:166180
|
Lacc1em1Arkr/Lacc1em1Arkr
(C57BL/6NTac-Lacc1em1Arkr)
|
abnormal redox activity
|
J:244365
|
Lacc1em2Arkr/Lacc1em2Arkr
(C57BL/6NTac-Lacc1em2Arkr)
|
abnormal redox activity
|
J:244365
|
Lacc1em3Arkr/Lacc1em3Arkr
(C57BL/6NTac-Lacc1em3Arkr)
|
abnormal redox activity
|
J:244365
|
Lacc1em4Arkr/Lacc1em4Arkr
(C57BL/6NTac-Lacc1em4Arkr)
|
abnormal redox activity
|
J:244365
|
Lacc1tm1a(KOMP)Wtsi/Lacc1tm1a(KOMP)Wtsi
(involves: C57BL/6N * C57BL/6NTac)
|
abnormal cellular respiration
|
J:244365
|
abnormal oxidative phosphorylation
|
J:244365
|
abnormal redox activity
|
J:244365
|
Lama1tm1.1Arhi/Lama1tm1.2Arhi Edil3Tg(Sox2-cre)1Amc/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal radial glial cell morphology
|
J:184432
|
Lama1tm1.1Olf/Lama1tm1.1Olf
(involves: 129S2/SvPas)
|
increased embryonic tissue cell apoptosis
|
J:102740
|
Lama2dy-2J/Lama2dy-2J
(B6.WK-Lama2dy-2J/J)
|
abnormal basal lamina morphology
|
J:134367
|
Lama2dy-2J/Lama2dy-2J Lama4tm1Ktry/Lama4tm1Ktry
(involves: 129X1/SvJ * C57BL/6 * WK/ReJ)
|
abnormal basal lamina morphology
|
J:98086
|
Lama2dy-2J/Lama2dy-2J Lama4tm1Ktry/Lama4tm1Ktry Tg(ACTB-Lama5)1Jhm/0
(involves: 129X1/SvJ * C57BL/6 * WK/ReJ)
|
abnormal basal lamina morphology
|
J:98086
|
Lama2dy-7J/Lama2dy-7J
(C57BL/6J-Lama2dy-7J/J)
|
abnormal basal lamina morphology
|
J:134367
|
Lama2dy/Lama2dy
(involves: 129P1/Re * C57BL/6)
|
abnormal basal lamina morphology
|
J:134367
|
Lama2dy/Lama2dy
(129P1/ReJ-Lama2dy/J)
|
abnormal basement membrane morphology
|
J:5866,
J:5565
|
Lama2tm1Eeng/Lama2tm1Eeng Smdt1tm1c(EUCOMM)Wtsi/Smdt1tm1c(EUCOMM)Wtsi Tg(Ckmm-cre)5Khn/0
(involves: 129S1/Sv * 129S4/SvJae * C57BL/6N * FVB)
|
abnormal mitochondrial physiology
|
J:287405
|
Lama2tm1Stk/Lama2tm1Stk
(involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR)
|
abnormal basal lamina morphology
|
J:43145
|
Lama2tm1Stk/Lama2tm1Stk
(involves: 129P2/OlaHsd)
|
abnormal basement membrane morphology
|
J:100711
|
decreased spermatid number
|
J:100711
|
Lama4tm1Ktry/Lama4tm1Ktry
(either: B6.129X1-Lama4tm1Ktry or (involves: 129X1/SvJ * C57BL/6))
|
impaired basement membrane formation
|
J:74287
|
Lama4tm1Ktry/Lama4tm1Ktry
(B6.129X1-Lama4tm1Ktry)
|
cardiac interstitial fibrosis
|
J:105789
|
Lama5tm1Jhm/Lama5tm1Jhm
(involves: 129 * C57BL/6J)
|
abnormal intestinal goblet cell morphology
|
J:84903
|
abnormal mesangial cell morphology
|
J:59925
|
impaired basement membrane formation
|
J:77264
|
Lama5tm1Jhm/Lama5tm2Jhm Tg(SFTPC-rtTA)5Jaw/? Tg(tetO-cre)1Jaw/?
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:104565
|
increased apoptosis
|
J:104565
|
Lama5tm3Jhm/Lama5tm3Jhm
(involves: 129S1/Sv * 129X1/SvJ)
|
increased kidney apoptosis
|
J:128225
|
Lamb2tm1Jrs/Lamb2tm1Jrs
(involves: 129S1/Sv * 129X1/SvJ)
|
increased retina apoptosis
|
J:77308
|
Lamc1tm1Strl/Lamc1tm1.2Strl
(either: (involves: 129P2/OlaHsd * C57BL/6 * CBA) or (involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * CBA))
|
abnormal basement membrane morphology
|
J:199683
|
Lamc1tm1Umr/Lamc1tm1Umr
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal basement membrane morphology
|
J:76368
|
Lamc1tm1Umr/Lamc1tm1Umr
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal basement membrane morphology
|
J:119018,
J:124247
|
abnormal neuron differentiation
|
J:124247
|
abnormal radial glial cell morphology
|
J:119018,
J:124247
|
Lamc2jeb/Lamc2jeb
(129X1/SvJ-Lamc2jeb)
|
abnormal basal lamina morphology
|
J:158873
|
Lamp1tm1Psa/Lamp1tm1Psa Lamp2tm1Psa/Y
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal lysosome morphology
|
J:92521
|
Lamp1tm1Psa/Lamp1tm1Psa Lamp2tm1Psa/Lamp2tm1Psa
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal lysosome morphology
|
J:92521
|
Lamp2tm1.2Ces/Y
(involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal autophagy
|
J:328713
|
Lamp2tm1Amcu/Y Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J)
|
abnormal autophagy
|
J:215605
|
cellular phenotype
|
J:215605
|
increased cellular glucose import
|
J:215605
|
increased hepatocyte apoptosis
|
J:215605
|
Lamp2tm1Psa/Lamp2tm1Psa
(either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv))
|
abnormal cell physiology
|
J:64151
|
Lamp2tm1Psa/Lamp2tm1Psa
(involves: 129P2/OlaHsd)
|
abnormal cellular respiration
|
J:253728
|
abnormal mitochondrial morphology
|
J:253728
|
abnormal mitophagy
|
J:253728
|
impaired autophagy
|
J:253728
|
Lamtor1tm1Moka/Lamtor1tm1Moka
(involves: C57BL/6)
|
abnormal lysosome morphology
|
J:168293
|
Lamtor2tm1.1Lah/Lamtor2tm1.1Lah Tg(KRT5-cre)1Tak/0
(involves: 129P2/OlaHsd * C3H * C57BL/6 * SJL)
|
decreased cell proliferation
|
J:119075
|
Lancl1tm1.1Pfw/Lancl1tm1.1Pfw
(involves: 129 * C57BL/6)
|
abnormal mitochondrial physiology
|
J:214805
|
abnormal redox activity
|
J:324139
|
abnormal sperm mitochondrial morphology
|
J:324139
|
abnormal spermatocyte morphology
|
J:324139
|
abnormal spermatogonia morphology
|
J:324139
|
abnormal spermatogonia proliferation
|
J:324139
|
asthenozoospermia
|
J:324139
|
decreased male germ cell number
|
J:324139
|
decreased sperm progressive motility
|
J:324139
|
dilated mitochondrion
|
J:324139
|
increased male germ cell apoptosis
|
J:324139
|
increased neuron apoptosis
|
J:214805
|
increased sperm mitochondrial size
|
J:324139
|
increased susceptibility to neuronal excitotoxicity
|
J:214805
|
oligozoospermia
|
J:324139
|
oxidative stress
|
J:324139,
J:214805
|
Lancl1tm1Pfw/Lancl1tm1.1Pfw Tg(Ddx4-cre)1Dcas/0
(involves: 129 * C57BL/6 * FVB)
|
asthenozoospermia
|
J:324139
|
decreased male germ cell number
|
J:324139
|
decreased sperm progressive motility
|
J:324139
|
oligozoospermia
|
J:324139
|
oxidative stress
|
J:324139
|
Laptm4bem1Huty/Laptm4bem1Huty
(C57BL/6-Laptm4bem1Huty)
|
abnormal lysosome morphology
|
J:310542
|
impaired autophagy
|
J:310542
|
Laptm5tm1Jow/Laptm5tm1Jow
(C57BL/6-Laptm5tm1Jow)
|
increased T cell proliferation
|
J:137841
|
Larp4tm1.1Rjma/Larp4tm1.1Rjma
(involves: C57BL/6)
|
abnormal fibroblast physiology
|
J:264766
|
Larp7tm1Ymat/Larp7tm1Ymat
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased primordial germ cell number
|
J:191206
|
decreased primordial germ cell proliferation
|
J:191206
|
Lat2tm1Wz/Lat2tm1Wz
(B6.Cg-Lat2tm1Wz)
|
increased T cell proliferation
|
J:116157
|
Lat2tm1Wz/Lat2tm1Wz
(Not Specified)
|
increased mast cell degranulation
|
J:181866
|
Lat2tm3.1Wz/Lat2tm3.1Wz
(B6.Cg-Lat2tm3.1Wz)
|
increased mast cell degranulation
|
J:181866
|
Lattm1.1Lov/Lattm1.1Lov
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased T cell proliferation
|
J:77099
|
increased T cell proliferation
|
J:77099
|
Lattm1.1Mal/Lattm1.1Mal
(involves: 129S2/SvPas)
|
increased T cell proliferation
|
J:77098
|
Lattm1.1Mal/Lattm1.1Mal
(involves: 129S2/SvPas * C57BL/6)
|
abnormal T cell proliferation
|
J:131351
|
Lats1tm1Noj/Lats1tm1Noj
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell physiology
|
J:200232
|
abnormal centrosome morphology
|
J:200232
|
abnormal mitosis
|
J:200232
|
abnormal mitotic spindle morphology
|
J:200232
|
increased fibroblast proliferation
|
J:200232
|
Lats2tm1Noj/Lats2tm1Noj
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell nucleus morphology
|
J:123480
|
abnormal intracellular organelle morphology
|
J:123480
|
abnormal mitosis
|
J:123480
|
increased cell nucleus count
|
J:123480
|
increased spinal cord apoptosis
|
J:123480
|
polyploidy
|
J:123480
|
Lats2tm1Noj/Lats2tm1Noj
(involves: 129S2/SvPas)
|
abnormal centrosome morphology
|
J:200232
|
Lats2tm1Raz/Lats2tm1Raz
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell proliferation
|
J:93191
|
chromosome breakage
|
J:93191
|
decreased cell proliferation
|
J:93191
|
Lbca1C57BL/6Igc/Lbca1C57BL/6Igc
(involves: BALB/cIgc * C57BL/6Igc)
|
increased B cell proliferation
|
J:139348
|
Lbca2BALB/cIgc/Lbca2C57BL/6Igc
(involves: BALB/cIgc * C57BL/6Igc)
|
increased B cell proliferation
|
J:139348
|
Lbca2C57BL/6Igc/Lbca2C57BL/6Igc
(involves: BALB/cIgc * C57BL/6Igc)
|
increased B cell proliferation
|
J:139348
|
LbrGt(XE569)Byg/LbrGt(XE569)Byg
(involves: 129P2/OlaHsd * C57BL/6Cr)
|
abnormal cell nucleus morphology
|
J:138854
|
abnormal granulocyte differentiation
|
J:138854
|
abnormal nuclear lamina morphology
|
J:138854
|
increased neuron apoptosis
|
J:138854
|
Lbric-J/Lbric-J
(C57BL/6J-Lbric-J)
|
abnormal cell nucleus morphology
|
J:80915
|
Lbric-J/Lbric-J
(involves: 129S4/SvJae * C57BL/6)
|
abnormal neutrophil differentiation
|
J:143838
|
Lbric/Lbr+
(Not Specified)
|
abnormal cell nucleus morphology
|
J:5569
|
Lbric/Lbric
(Not Specified)
|
abnormal cell nucleus morphology
|
J:5569
|
increased mitochondrial fission
|
J:5740
|
Lbrlym3/Lbrlym3
(C57BL/6-Lbrlym3)
|
decreased T cell proliferation
|
J:180355
|
Lbx1tm1.1Khan/Lbx1tm1.1Khan Myf5tm3(cre)Sor/Myf5+
(involves: 129S4/SvJaeSor * C57BL/6JJcl * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal muscle precursor cell migration
|
J:178868
|
Lbx1tm1Cbm/Lbx1tm1Cbm Olig3tm1Tre/Olig3tm1Tre
(involves: 129P2/OlaHsd)
|
abnormal neuron differentiation
|
J:96749
|
Lbx1tm1Gld/Lbx1tm1Gld
(involves: 129S1/Sv * C57BL/6)
|
abnormal muscle precursor cell migration
|
J:56498
|
Lbx1tm1Thbr/Lbx1tm1Thbr
(involves: 129S4/SvJae)
|
abnormal muscle precursor cell migration
|
J:57891
|
Lbx1tm2Cbm/Lbx1tm3.1(cre)Cbm Mapttm2Arbr/Mapt+
(involves: 129P2/OlaHsd)
|
abnormal neuron differentiation
|
J:121332
|
Lcattm1Hgc/Lcattm1Hgc
(involves: 129 * C57BL/6 * C57BL/6J * SJL)
|
increased mesangial cell number
|
J:93775
|
Lcattm1Hgc/Lcattm1Hgc Tg(SREBP1a)7343Reh/?
(involves: 129 * C57BL/6 * C57BL/6J * SJL)
|
increased mesangial cell number
|
J:93775
|
Lcattm1Nsa/Lcattm1Nsa
(B6.Cg-Lcattm1Nsa)
|
increased mesangial cell number
|
J:69299
|
Lcktm1Dbs/Lcktm1Dbs
(involves: C3H * C57BL/6)
|
decreased T cell proliferation
|
J:114660
|
Lcktm1Dbs/Lcktm1Dbs Tg(TcraTcrb)1100Mjb/0
(involves: C3H * C57BL/6)
|
decreased T cell proliferation
|
J:114660
|
Lcktm1Litt/Lcktm1.1Litt Tnfrsf4tm2(cre)Nik/Tnfrsf4+
(involves: 129X1/SvJ)
|
decreased T cell proliferation
|
J:152472
|
Lclat1tm1Yugs/Lclat1tm1Yugs
(B6.Cg-Lclat1tm1Yugs)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:163077
|
increased fatty acid oxidation
|
J:163077
|
Lcn2tm1Mrgr/Lcn2tm1Mrgr
(129(B6)-Lcn2tm1Mrgr)
|
decreased apoptosis
|
J:173490
|
decreased thymocyte apoptosis
|
J:173490
|
Lcn8em1Jgao/Lcn8em1Jgao
(C57BL/6-Lcn8em1Jgao)
|
abnormal sperm head morphology
|
J:305282
|
absent sperm head
|
J:305282
|
asthenozoospermia
|
J:305282
|
coiled sperm flagellum
|
J:305282
|
decreased sperm progressive motility
|
J:305282
|
teratozoospermia
|
J:305282
|
Lcp2tm1.1Wz/Lcp2tm1.1Wz
(B6.Cg-Lcp2tm1.1Wz)
|
decreased T cell proliferation
|
J:150304
|
Lcp2tm2Gak/Lcp2tm2Gak Tg(Cd4-cre)1Cwi/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
decreased T cell apoptosis
|
J:107467
|
Ldb1tm1Lmgd/Ldb1tm1Lmgd
(involves: CD-1)
|
abnormal primordial germ cell morphology
|
J:81152
|
Ldhctm1Erg/Ldhctm1Erg
(involves: 129S6/SvEvTac * C57BL/6N)
|
asthenozoospermia
|
J:132072
|
LdlrHlb301/Ldlr+
(C57BL/6J-LdlrHlb301/J)
|
increased macrophage derived foam cell number
|
J:82961
|
LdlrHlb301/LdlrHlb301
(C57BL/6J-LdlrHlb301/J)
|
increased macrophage derived foam cell number
|
J:82961
|
Ldlrtm1Her/Ldlrtm1Her
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased hepatocyte apoptosis
|
J:175559
|
maternal effect
|
J:146932
|
oxidative stress
|
J:175559
|
Ldlrtm1Her/Ldlrtm1Her Lrp1tm2Her/Lrp1tm2Her Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S7/SvEvBrd)
|
impaired macrophage phagocytosis
|
J:137404
|
Ldlrtm1Her/Ldlrtm1Her Lrp1tm2Her/Lrp1tm2Her Tg(Tagln-cre)1Her/0
(involves: 129S7/SvEvBrd * C57BL/6J * SJL)
|
increased vascular smooth muscle cell proliferation
|
J:82871
|
Ldlrtm1Her/Ldlrtm1Her Mapkapk2tm1Mgl/Mapkapk2tm1Mgl
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6)
|
abnormal macrophage derived foam cell morphology
|
J:142788
|
Ldlrtm1Her/Ldlrtm1Her Pfn1tm1Wit/Pfn1+
(B6.129S-Ldlrtm1Her Pfn1tm1Wit)
|
impaired macrophage chemotaxis
|
J:140294
|
Ldlrtm1Her/Ldlrtm1Her Tlr2tm1Kir/Tlr2tm1Kir
(B6.129-Tlr2tm1Kir Ldlrtm1Her)
|
abnormal cellular extravasation
|
J:131783
|
Ldlrtm1Her/Ldlrtm1Her Vwftm1Wgr/Vwftm1Wgr
(B6.129S-Vwftm1Wgr Ldlrtm1Her)
|
impaired leukocyte tethering or rolling
|
J:106677
|
Ldlrtm1Her/Ldlrtm1Her Wnt16tm2a(EUCOMM)Wtsi/Wnt16tm2a(EUCOMM)Wtsi
(involves: 129S7/SvEvBrd * C57BL/6J * C57BL/6N)
|
abnormal mitochondrial crista morphology
|
J:344215
|
abnormal mitochondrial matrix morphology
|
J:344215
|
abnormal mitochondrial physiology
|
J:344215
|
abnormal muscle fiber mitochondrial morphology
|
J:344215
|
dilated mitochondrion
|
J:344215
|
Leat1Tg(Tyr)442Ove/Leat1Tg(Tyr)442Ove
(FVB/NJ-Leat1Tg(Tyr)442Ove)
|
maternal effect
|
J:284089
|
Lect2tm1Ymg/Lect2tm1Ymg
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased T cell apoptosis
|
J:90961
|
Lef1tm1Rug/Lef1tm1Rug
(involves: 129S2/SvPas * C57BL/6)
|
abnormal vascular regression
|
J:144980
|
Lefty1tm1Hmd/Lefty1tm1Hmd Tg(Hhex-EGFP)#Rbe/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA/J)
|
abnormal anterior visceral endoderm cell migration
|
J:170681
|
Lemd2Gt(DD0639)Wtsi/Lemd2Gt(DD0639)Wtsi
(B6.129P2-Lemd2Gt(DD0639)Wtsi)
|
impaired neuron differentiation
|
J:221495
|
increased embryonic neuroepithelium apoptosis
|
J:221495
|
Lemd3Gt(XST167)Byg/Lemd3Gt(XST167)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:119566
|
increased embryonic tissue cell apoptosis
|
J:119566
|
Lepob/Lepob
(involves: C57BL/6J)
|
abnormal colon goblet cell morphology
|
J:109110
|
abnormal osteoclast differentiation
|
J:60001
|
abnormal respiratory electron transport chain
|
J:116841
|
Lepob/Lepob
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:164339
|
Lepob/Lepob
(B6.Cg-Lepob/JRj)
|
abnormal cell cycle
|
J:220381
|
increased hepatocyte apoptosis
|
J:277927
|
oxidative stress
|
J:220381
|
Lepob/Lepob Ppargtm2Avp/Ppargtm2Avp
(involves: 129 * C57BL/6)
|
oxidative stress
|
J:121534
|
Lepob/Lepob Sesn2Gt(RRJ141)Byg/Sesn2Gt(RRJ141)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased fatty acid beta-oxidation
|
J:189021
|
Leprdb-9J/Leprdb-9J
(involves: C57BL/6 * CBA * SWR)
|
decreased oocyte number
|
J:129982
|
Leprdb/Lepr+
(involves: C57BLKS/J)
|
maternal effect
|
J:219658
|
Leprdb/Leprdb
(involves: C57BLKS/J)
|
abnormal aerobic respiration
|
J:106871,
J:107138
|
abnormal respiratory electron transport chain
|
J:106871
|
Leprdb/Leprdb
(BKS.Cg-Dock7m +/+ Leprdb/J)
|
abnormal axon extension
|
J:112680
|
Leprdb/Leprdb
(involves: C57BL/6)
|
abnormal osteoclast differentiation
|
J:60001
|
Leprdb/Leprdb
(BKS.Cg-Dock7m +/+ Leprdb/Jcl)
|
increased pancreatic islet cell apoptosis
|
J:156725
|
Leprdb/Leprdb
(B6.BKS(D)-Leprdb/JOrlRj)
|
increased hepatocyte apoptosis
|
J:277927
|
Leprdb/Leprdb Rock1tm1Leiw/Rock1tm1Leiw
(involves: 129S7/SvEvBrd * C57BLKS/J * FVB/N)
|
abnormal mitochondrial physiology
|
J:182287
|
increased renal glomerulus apoptosis
|
J:182287
|
oxidative stress
|
J:182287
|
Leprm7Btlr/Leprm7Btlr
(C57BL/6J-Leprm7Btlr)
|
decreased cell death
|
J:236685
|
Leprtm1.1Rll/Lepr+
(129P3/J-Leprtm1.1Rll)
|
increased enterocyte apoptosis
|
J:172012
|
Leprtm1.1Rll/Leprtm1.1Rll
(129P3/J-Leprtm1.1Rll)
|
increased enterocyte apoptosis
|
J:172012
|
Leprtm4Mgmj/Leprtm4Mgmj
(B6.Cg-Leprtm4Mgmj)
|
decreased T cell proliferation
|
J:164339
|
Letm1Gt(CC0204)Wtsi/Letm1+
(129S.129P2-Letm1Gt(CC0204)Wtsi)
|
abnormal mitochondrial physiology
|
J:222017
|
Letm1Gt(DD0926)Wtsi/Letm1+
(129S.129P2-Letm1Gt(DD0926)Wtsi)
|
abnormal mitochondrial physiology
|
J:222017
|
Lfngtm1Rjo/Lfngtm1Rjo
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal female meiosis
|
J:96967
|
abnormal oocyte morphology
|
J:96967
|
Lgals2tm1.1Cfg/Lgals2tm1.1Cfg
(involves: C57BL/6)
|
decreased apoptosis
|
J:217719
|
Lgals3tm1Ftl/Lgals3tm1Ftl
(involves: 129S2/SvPas * C57BL/6)
|
decreased male germ cell number
|
J:313172
|
increased macrophage apoptosis
|
J:60741
|
increased male germ cell apoptosis
|
J:313172
|
Lgals3tm1Ftl/Lgals3tm1Ftl
(involves: 129S2/SvPas * CD-1)
|
oxidative stress
|
J:116073
|
Lgals3tm1Poi/Lgals3tm1Poi
(involves: 129/Sv * C57BL/6 * SJL)
|
impaired macrophage chemotaxis
|
J:131971
|
impaired macrophage phagocytosis
|
J:131407
|
Lgals7tm1Ijmfp/Lgals7tm1Ijmfp
(involves: 129 * C57BL/6 * SJL)
|
decreased keratinocyte migration
|
J:263069
|
increased keratinocyte apoptosis
|
J:263069
|
increased keratinocyte proliferation
|
J:263069
|
Lgals9tm1.1Cfg/Lgals9tm1.1Cfg
(involves: C57BL/6)
|
increased B cell proliferation
|
J:217719
|
Lgmntm1Cptr/Lgmntm1Cptr
(B6.129S6-Lgmntm1Cptr)
|
lysosomal protein accumulation
|
J:172774
|
Lgmntm1Ihn/Lgmntm1Ihn
(involves: 129P2/OlaHsd * C57BL/6J)
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:85207
|
Lgr4Gt(pU-21)1Kymm/Lgr4Gt(pU-21)1Kymm
(CBA.Cg-Lgr4Gt(pU-21)1Kymm)
|
asthenozoospermia
|
J:121125
|
Lgr4tm1.1(cre/ERT2)Npa/Lgr4tm1.1(cre/ERT2)Npa
(involves: C57BL/6)
|
abnormal epidermal stem cell proliferation
|
J:212415
|
Lgr4tm1.1(cre/ERT2)Npa/Lgr4tm1.1(cre/ERT2)Npa Lgr5tm1.1(cre/ERT2)Npa/Lgr5tm1.1(cre/ERT2)Npa
(involves: C57BL/6)
|
abnormal epidermal stem cell proliferation
|
J:212415
|
decreased kidney cell proliferation
|
J:212415
|
Lgr4tm1.1Knis/Lgr4tm1.1Knis Lgr5tm2.1Cle/Lgr5tm2.1Cle Tg(Cyp1a1-cre)1Dwi/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal small intestinal crypt cell proliferation
|
J:174842
|
Lgr4tm1.1Knis/Lgr4tm1.1Knis Tg(Cyp1a1-cre)1Dwi/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal small intestinal crypt cell proliferation
|
J:174842
|
Lgr4tm1.2Knis/Lgr4tm1.2Knis
(B6.129P2-Lgr4tm1.2Knis)
|
increased kidney apoptosis
|
J:186318
|
Lgr5tm1(cre/ERT2)Cle/Lgr5+ Stk26tm2.1Zzh/Stk26tm2.1Zzh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal enterocyte proliferation
|
J:322311
|
Lhbtm1Kmr/Lhbtm1Kmr
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal male germ cell apoptosis
|
J:122322
|
azoospermia
|
J:94719,
J:122322
|
decreased elongated spermatid number
|
J:122322
|
decreased oocyte number
|
J:94719
|
Lhcgrtm1Hht/Lhcgrtm1Hht
(involves: 129S7/SvEvBrd * C57BL/6J)
|
oligozoospermia
|
J:105533
|
Lhcgrtm1Zmlei/Lhcgrtm1Zmlei
(either: 129X1/SvJ-Lhcgrtm1Zmlei or (involves: 129X1/SvJ * C57BL/6))
|
increased male germ cell apoptosis
|
J:82008
|
Lhx1tm1Bhr/Lhx1tm2.1Rob Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S/SvEv * C57BL/6 * C57BL/6N * CBA)
|
cellular necrosis
|
J:226614
|
Lhx1tm1Tmj/Lhx1+ Rettm1.1Kln/Rettm1.1Kln
(involves: 129/Sv * BALB/c * C57BL/6 * CBA/J)
|
abnormal axon guidance
|
J:110955
|
Lhx1tm1Tmj/Lhx1+ Rettm1Kln/Rettm1Kln Tg(Nes-cre)1Kln/0
(involves: 129/Sv * BALB/c * C57BL/6 * CBA/J * SJL)
|
abnormal axon guidance
|
J:110955
|
Lhx3tm1.1Sjr/Lhx3tm1.1Sjr
(involves: 129S/SvEv * C57BL/6J * FVB/N)
|
azoospermia
|
J:169035
|
Lhx5tm1Lmgd/Lhx5tm1Lmgd
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal axon guidance
|
J:55103
|
abnormal neuronal migration
|
J:55103
|
abnormal neuronal precursor proliferation
|
J:55103
|
Lhx6tm1Vpa/Lhx6tm2Vpa
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuron differentiation
|
J:198547
|
Lhx6tm2Vpa/Lhx6tm2Vpa
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
abnormal neuronal migration
|
J:119476
|
decreased neuronal migration
|
J:119476
|
Lhx8tm1Lmgd/Lhx8tm1Lmgd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal oogenesis
|
J:294629
|
Lhx8tm1Lmgd/Lhx8tm1Lmgd
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6)
|
absent oocytes
|
J:140898
|
decreased oocyte number
|
J:140898
|
oocyte degeneration
|
J:140898
|
Lhx8tm1Lmgd/Lhx8tm1Lmgd
(involves: 129 * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:262653
|
abnormal mitophagy
|
J:262653
|
decreased oocyte number
|
J:262653
|
enhanced autophagy
|
J:262653
|
increased ovary apoptosis
|
J:262653
|
oocyte degeneration
|
J:262653
|
Lhx8tm1Vpa/Lhx8tm2.1Vpa Tg(Chat-cre)GM24Gsat/0
(involves: 129P2/OlaHsd * 129S4/SvJae * FVB/N)
|
abnormal neuron differentiation
|
J:182013
|
Lhx9tm1Lmgd/Lhx9tm1Lmgd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased primordial germ cell proliferation
|
J:60621
|
Liftm1Phb/Lif+
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:77410
|
Liftm1Phb/Liftm1Phb
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:77410
|
Liftm1Stw/Liftm1Stw
(involves: 129S1/Sv * C57BL/6)
|
increased vascular endothelial cell proliferation
|
J:137720
|
Liftm1Stw/Liftm1Stw
(involves: 129S1/Sv * MF1)
|
abnormal osteoclast differentiation
|
J:137646
|
Lig1tm1Dwm/Lig1tm1Dwm
(involves: 129P2/OlaHsd)
|
abnormal DNA replication
|
J:75962
|
cellular phenotype
|
J:75962
|
chromosomal instability
|
J:75962
|
decreased fibroblast proliferation
|
J:75962
|
Lig1tm3Dwm/Lig1tm3Dwm
(involves: 129P2/OlaHsd * C57BL/6)
|
chromosomal instability
|
J:77902
|
decreased fibroblast proliferation
|
J:77902
|
Lig3tm1.1Pmc/Lig3tm1.1Pmc Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
abnormal cellular respiration
|
J:170077
|
abnormal DNA repair
|
J:170077
|
abnormal neuron differentiation
|
J:170077
|
abnormal neuronal precursor proliferation
|
J:170077
|
Lig3tm1Czhu/Lig3tm1Czhu
(involves: 129)
|
elevated level of mitotic sister chromatid exchange
|
J:109063
|
Lig4tiny/Lig4tiny
(C57BL/6-Lig4tiny)
|
abnormal DNA repair
|
J:122725
|
decreased fibroblast proliferation
|
J:122725
|
Lig4tm1Fwa/Lig4+
(involves: 129S6/SvEvTac * C57BL/6)
|
chromosome breakage
|
J:80467
|
Lig4tm1Fwa/Lig4tm1Fwa
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell physiology
|
J:50865
|
chromosome breakage
|
J:80467
|
decreased cell proliferation
|
J:50865
|
increased cellular sensitivity to gamma-irradiation
|
J:50865
|
Lig4tm1Fwa/Lig4tm1Fwa
(involves: 129S6/SvEvTac)
|
abnormal cell physiology
|
J:110848
|
chromosomal instability
|
J:147247
|
increased cellular sensitivity to ionizing radiation
|
J:147247
|
increased forebrain apoptosis
|
J:110848
|
increased spinal cord apoptosis
|
J:110848
|
induced chromosome breakage
|
J:147247
|
Lig4tm1Fwa/Lig4tm1Fwa Tg(Cr2-cre)3Cgn/0 Xrcc4tm2Fwa/Xrcc4tm2Fwa
(involves: 129S6/SvEvTac)
|
increased cellular sensitivity to ionizing radiation
|
J:126758
|
spontaneous chromosome breakage
|
J:126758
|
Lig4tm1Fwa/Lig4tm1Fwa Trp53tm1Brd/Trp53+
(involves: 129S6/SvEvTac * 129S7/SvEvBrd)
|
decreased neuron apoptosis
|
J:63078
|
Lig4tm1Fwa/Lig4tm1Fwa Trp53tm1Brd/Trp53tm1Brd
(involves: 129S6/SvEvTac * 129S7/SvEvBrd)
|
decreased neuron apoptosis
|
J:63078
|
increased cellular sensitivity to ionizing radiation
|
J:63078
|
increased fibroblast proliferation
|
J:63078
|
Lig4tm1Icrf/Lig4tm1Icrf
(involves: 129)
|
cellular phenotype
|
J:144172
|
Lig4tm1Icrf/Lig4tm1Icrf
(either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv * 129X1/SvJ))
|
increased neuron apoptosis
|
J:111068,
J:51608,
J:65540
|
Lig4tm1Icrf/Lig4tm1Icrf Mre11atm1Jpt/Mre11atm1Jpt
(involves: 129 * 129S7/SvEvBrd)
|
decreased cellular sensitivity to ionizing radiation
|
J:144172
|
Lig4tm1Icrf/Lig4tm1Icrf Nbntm1Jpt/Nbntm1Jpt
(involves: 129 * 129S7/SvEvBrd)
|
cellular phenotype
|
J:144172
|
Lig4tm1Pmc/Lig4tm1Pmc Tg(Nes-cre)1Kln/0
(involves: 129S1/SvImJ * C57BL/6 * SJL)
|
abnormal DNA repair
|
J:144172
|
Lig4tm1Pmc/Lig4tm1Pmc Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * C57BL/6 * SJL)
|
abnormal double-strand DNA break repair
|
J:226703
|
Lig4tm2.1Fwa/Lig4tm2.1Fwa
(involves: 129S6/SvEvTac)
|
abnormal cell physiology
|
J:157574
|
chromosomal instability
|
J:157574
|
decreased T cell proliferation
|
J:157574
|
increased cellular sensitivity to gamma-irradiation
|
J:157574
|
increased T cell apoptosis
|
J:157574
|
spontaneous chromosome breakage
|
J:157574
|
Lilrb4atm1Eol/Lilrb4atm1Eol
(B6.129P2-Lilrb4atm1Eol)
|
abnormal cellular extravasation
|
J:129969
|
increased mast cell degranulation
|
J:129969
|
Lilrb4atm1Hrk/Lilrb4atm1Hrk
(involves: 129/Sv * BALB/c)
|
increased mast cell degranulation
|
J:70491
|
Limk1tm1Zpj/Limk1tm1Zpj
(involves: 129)
|
abnormal actin cytoskeleton morphology
|
J:86283
|
Limk2tm1.1Tnak/Limk2tm1.1Tnak
(either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
abnormal spermatocyte morphology
|
J:73966
|
increased male germ cell apoptosis
|
J:73966
|
Lims1tm1.2Chen/Lims1tm1.2Chen
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss)
|
abnormal cell death
|
J:97635
|
decreased cell proliferation
|
J:97635
|
Lin7ctm1Dsb/Lin7ctm1Dsb
(involves: 129S1/Sv * 129X1/SvJ)
|
increased kidney apoptosis
|
J:134806
|
Lin7ctm2Dsb/Lin7ctm2Dsb Tg(Pax3-cre)1Joe/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
increased kidney apoptosis
|
J:134806
|
Lin9Gt(RRI306)Byg/Lin9Gt(RRI306)Byg
(involves: 129P2/OlaHsd)
|
absent inner cell mass proliferation
|
J:162678
|
Lin28atm1.1Gqda/Lin28atm1.1Gqda
(involves: 129S4/SvJae * C57BL/6 * FVB)
|
decreased germ cell number
|
J:196313
|
Lin28atm1.1Gqda/Lin28atm1.1Gqda
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell physiology
|
J:199720
|
Lin28atm1Egm/Lin28atm1Egm
(involves: 129S/SvEv * C57BL/6NTac)
|
decreased germ cell number
|
J:196313
|
decreased oocyte number
|
J:196313
|
decreased primordial germ cell number
|
J:196313
|
oligozoospermia
|
J:196313
|
Lipatm1c(EUCOMM)Hmgu/Lipatm1c(EUCOMM)Hmgu Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1Tg(Alb-cre)21Mgn
(involves: C57BL/6J * C57BL/6N * C57BL/6NTac)
|
abnormal lipid oxidation
|
J:270182
|
abnormal tricarboxylic acid cycle
|
J:270182
|
Lipetm1Gam/Lipetm1Gam
(involves: 129S4/SvJae)
|
abnormal spermatid morphology
|
J:71782
|
azoospermia
|
J:71782
|
decreased elongated spermatid number
|
J:71782
|
decreased male germ cell number
|
J:71782
|
Lipetm1Ishi/Lipetm1Ishi
(involves: 129S7/SvEvBrd * C57BL/6)
|
asthenozoospermia
|
J:59889
|
oligozoospermia
|
J:59889
|
Lipetm1Land/Lipetm1Land
(involves: 129 * C57BL/6J)
|
decreased skeletal muscle cell glucose uptake
|
J:85540
|
oligozoospermia
|
J:85540
|
Litaftm1.1Cwc/Litaf+
(B6.Cg-Litaftm1.1Cwc)
|
abnormal exocytosis
|
J:314784
|
abnormal lysosome physiology
|
J:314784
|
abnormal vacuole morphology
|
J:314784
|
cellular phenotype
|
J:314784
|
Litaftm1.1Cwc/Litaftm1.1Cwc
(B6.Cg-Litaftm1.1Cwc)
|
abnormal exocytosis
|
J:314784
|
abnormal lysosome physiology
|
J:314784
|
abnormal vacuole morphology
|
J:314784
|
cellular phenotype
|
J:314784
|
Litaftm1.1Ics/Litaftm1.1Ics
(Not Specified)
|
impaired macrophage chemotaxis
|
J:186411
|
Litaftm1.2Cwc/Litaftm1.2Cwc
(C57BL/6-Litaftm1.2Cwc)
|
abnormal exocytosis
|
J:314784
|
abnormal lysosome physiology
|
J:314784
|
abnormal vacuole morphology
|
J:314784
|
Litchiem1Jnch/Litchiem1Jnch
(involves: C57BL/6J)
|
delayed axon extension
|
J:345795
|
Llgl1tm1.1Vv/Llgl1tm1.1Vv
(Not Specified)
|
abnormal neuron differentiation
|
J:89028
|
abnormal neuronal precursor proliferation
|
J:89028
|
Llgl1tm1Vv/Llgl1tm1Vv Meox2tm1(cre)Sor/Meox2+
(involves: 129 * 129S4/SvJaeSor * C57BL/6J)
|
abnormal neuron differentiation
|
J:89028
|
abnormal neuronal precursor proliferation
|
J:89028
|
Lman1Gt(XST010)Byg/Lman1Gt(XST010)Byg
(B6.129P2-Lman1Gt(XST010)Byg)
|
abnormal endoplasmic reticulum morphology
|
J:177067
|
cellular phenotype
|
J:177067
|
Lmbrd1tm1.1Ntum/Lmbrd1+
(B6.Cg-Lmbrd1tm1.1Ntum)
|
abnormal cardiac muscle cell glucose uptake
|
J:204994
|
increased cardiac muscle cell glucose uptake
|
J:204994
|
LmnaDhe/Lmna+
(B6(D2)-LmnaDhe/TyGrsrJ)
|
abnormal cell cycle
|
J:171665
|
abnormal cell nucleus morphology
|
J:171665
|
abnormal DNA replication
|
J:171665
|
abnormal mitosis
|
J:171665
|
abnormal mitotic spindle assembly checkpoint
|
J:171665
|
abnormal nuclear lamina morphology
|
J:171665,
J:160175,
J:188496
|
aneuploidy
|
J:171665
|
decreased fibroblast proliferation
|
J:171665
|
increased middle ear goblet cell number
|
J:188496
|
LmnaDhe/LmnaDhe
(B6(D2)-LmnaDhe/TyGrsrJ)
|
abnormal nuclear lamina morphology
|
J:160175
|
Lmnaem1Fenz/Lmna+
(C57BL/6-Lmnaem1Fenz)
|
abnormal respiratory electron transport chain
|
J:338760
|
LmnaGt(S7-1F1)Sor/LmnaGt(S7-1F1)Sor
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal fat cell differentiation
|
J:221850
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:221850
|
Lmnatm1.1Otin/Lmna+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:177632,
J:177575
|
Lmnatm1.1Otin/Lmnatm1.1Otin
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:177632,
J:177575
|
abnormal cell physiology
|
J:177632
|
Lmnatm1.1Otin/Lmnatm1.1Otin
(involves: 129P2/OlaHsd * C57BL/6NTac)
|
oligozoospermia
|
J:261974
|
Lmnatm1Lgf/Lmna+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:141165,
J:100220,
J:146099
|
Lmnatm1Lgf/Lmnatm1Lgf
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:141165,
J:113119
|
Lmnatm1Rben/Lmnatm1Rben
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal chromosomal synapsis
|
J:223056
|
abnormal double-strand DNA break repair
|
J:223056
|
abnormal female meiosis
|
J:223056
|
abnormal meiosis
|
J:223056
|
arrest of male meiosis
|
J:223056
|
azoospermia
|
J:223056
|
Lmnatm1Stw/Lmna+
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:58702
|
Lmnatm1Stw/Lmna+ Zmpste24tm1Sgy/Zmpste24tm1Sgy
(involves: 129S1/Sv * 129S4/SvJae * C57BL/6)
|
cellular phenotype
|
J:95274
|
Lmnatm1Stw/Lmnatm1Stw
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:58702
|
Lmnatm1Stw/Lmnatm1Stw
(involves: 129S1/Sv * C57BL/6)
|
arrest of male meiosis
|
J:88595
|
azoospermia
|
J:88595
|
Lmnatm1Stw/Lmnatm7Lgf
(involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6)
|
abnormal cell nucleus morphology
|
J:165928
|
Lmnatm2.1Gbon/Lmnatm2.1Gbon
(involves: 129 * C57BL/6)
|
abnormal cell differentiation
|
J:180603
|
Lmnatm2Lgf/Lmna+ Zmpste24tm1Sgy/Zmpste24tm1Sgy
(involves: 129S4/SvJae * C57BL/6)
|
cellular phenotype
|
J:106473
|
Lmnatm2Lgf/Lmnatm7Lgf
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
abnormal cell nucleus morphology
|
J:165928
|
Lmnatm2Stw/Lmnatm2Stw
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:83382
|
Lmnatm3Lgf/Lmnatm3Lgf
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:141165
|
Lmnatm3Lgf/Lmnatm3Lgf
(involves: 129P2/OlaHsd)
|
abnormal cell nucleus morphology
|
J:167229
|
Lmnatm3Stw/Lmnatm3Stw
(involves: 129S1/Sv * 129S4/SvJaeSor * C57BL)
|
cardiac interstitial fibrosis
|
J:100393
|
Lmnatm4Lgf/Lmna+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:146099
|
Lmnatm5Lgf/Lmnatm5Lgf
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:160705
|
Lmnatm6Lgf/Lmnatm6Lgf
(involves: 129P2/OlaHsd)
|
abnormal cell nucleus morphology
|
J:165928
|
Lmnatm7Lgf/Lmna+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:165928
|
Lmnatm7Lgf/Lmnatm7Lgf
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:165928
|
Lmnatm8Lgf/Lmnatm8Lgf
(involves: 129P2/OlaHsd)
|
abnormal cell nucleus morphology
|
J:167229
|
Lmnb1Gt(XA130)Byg/Lmnb1Gt(XA130)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell differentiation
|
J:91473
|
abnormal cell nucleus morphology
|
J:91473
|
decreased cell proliferation
|
J:91473
|
Lmnb1tm1Yxz/Lmnb1tm1Yxz
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6)
|
abnormal neuronal migration
|
J:178993
|
abnormal neuronal precursor proliferation
|
J:178993
|
Lmnb1tm1Yxz/Lmnb1tm1Yxz Lmnb2tm1Yxz/Lmnb2tm1Yxz
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6)
|
abnormal cell physiology
|
J:178993
|
abnormal neuron differentiation
|
J:178993
|
abnormal neuronal migration
|
J:178993
|
abnormal neuronal precursor proliferation
|
J:178993
|
Lmnb1tm2Sgy/Lmnb1tm2Sgy
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:197315
|
Lmnb2tm1Ccof/Lmnb2tm1Ccof
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuronal migration
|
J:158610
|
abnormal neuronal precursor proliferation
|
J:158610
|
Lmnb2tm1Yxz/Lmnb2tm1Yxz
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6)
|
abnormal neuronal migration
|
J:178993
|
abnormal neuronal precursor proliferation
|
J:178993
|
Lmnb2tm2Sgy/Lmnb2tm2Sgy
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:197315
|
Lmo2tm1Thr/Lmo2tm1Thr
(either: (involves: 129P2/OlaHsd * MF1) or (involves: 129/Sv * 129P2/OlaHsd))
|
abnormal cell death
|
J:19175
|
Lmo4tm1.1Gng/Lmo4tm1.1Gng
(involves: 129X1/SvJ)
|
increased embryonic neuroepithelium apoptosis
|
J:96957
|
Lmod2tm1(KOMP)Vlcg/Lmod2tm1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
decreased mitochondrial number
|
J:227272
|
Lmr7BALB/cHeA/?
(involves: BALB/cHeA * STS/A)
|
decreased splenocyte proliferation
|
J:108764
|
Lmr18BALB/cHeA/Lmr18BALB/cHeA
(involves: BALB/cHeA * STS/A)
|
decreased splenocyte proliferation
|
J:108764
|
Lmr18BALB/cHeA/Lmr18CcS20/Dem
(involves: BALB/cHeA * STS/A)
|
decreased splenocyte proliferation
|
J:108764
|
Lmtk2tm1Tya/Lmtk2tm1Tya
(involves: 129P2/OlaHsd * C57BL/6)
|
azoospermia
|
J:118247
|
Lmx1adr-J/Lmx1adr-J
(involves: C3H * C57BL/6)
|
abnormal cell physiology
|
J:14476
|
abnormal cell proliferation
|
J:1460
|
abnormal neuronal migration
|
J:1460
|
Lmx1atm1Ics/Lmx1atm1Ics
(involves: C57BL/6J)
|
abnormal neuron differentiation
|
J:175535
|
Lmx1atm1Tpe/Lmx1atm1Tpe Lmx1btm1Zfc/Lmx1btm1Zfc Slc6a3tm1(cre)Lrsn/Slc6a3+
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6)
|
abnormal autophagy
|
J:222854
|
abnormal lysosome morphology
|
J:222854
|
abnormal lysosome physiology
|
J:222854
|
Lncbarem1Bcgen/Lncbarem1Bcgen
(involves: C57BL/6)
|
increased neuron apoptosis
|
J:316179
|
Lncucc1em1Bwu/Lncucc1em1Bwu
(C57BL/6-Lncucc1em1Bwu)
|
abnormal enterocyte proliferation
|
J:340220
|
increased enterocyte apoptosis
|
J:340220
|
Lonp1tm1Otin/Lonp1tm1Otin
(Not Specified)
|
decreased mitochondrial DNA content
|
J:221992
|
Loxl2tm1.2Acan/Loxl2tm1.2Acan
(Not Specified)
|
abnormal keratinocyte differentiation
|
J:220689
|
Lpar4tm1Sati/Y
(involves: C57BL/6)
|
abnormal cellular extravasation
|
J:253134
|
Lpar4tm1Sati/Lpar4+
(involves: C57BL/6)
|
abnormal cellular extravasation
|
J:253134
|
Lpar4tm1Sati/Lpar4tm1Sati
(involves: C57BL/6)
|
abnormal cellular extravasation
|
J:253134
|
Lpar6tm1.1Sati/Lpar6tm1.1Sati
(involves: C57BL/6 * C57BL/6NJcl * CBA)
|
abnormal cellular extravasation
|
J:253134
|
Lpin1fld/Lpin1fld
(involves: BALB/cByJ)
|
abnormal spermatocyte morphology
|
J:169933
|
Lpin3tm1Reue/Lpin3tm1Reue
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal fat cell differentiation
|
J:220917
|
Lpltm1Ijg/Lpltm1Ijg Tg(Myh6-cre)2182Mds/?
(involves: C57BL/6)
|
increased cardiac muscle cell glucose uptake
|
J:90737
|
Lpltm1Ijg/Lpltm1Ijg Tg(Myh6-cre)2182Mds/0
(involves: FVB/N)
|
cardiac interstitial fibrosis
|
J:110484
|
increased cardiac muscle cell glucose uptake
|
J:110484
|
Lpoem1Zlu/Lpoem1Zlu
(involves: C57BL/6 * SJL)
|
abnormal intestinal goblet cell morphology
|
J:307289
|
increased colon goblet cell number
|
J:307289
|
Lpptm1Wjmv/Lpptm1Wjmv
(B6.129P2-Lpptm1Wjmv)
|
abnormal cell death
|
J:144517
|
Lrattm1Log/Lrattm1Log
(involves: 129S1/Sv * C57BL/6J)
|
oligozoospermia
|
J:104101
|
Lrch1em1Hwa/Lrch1em1Hwa
(Not Specified)
|
abnormal cellular extravasation
|
J:238772
|
Lrfn2Tg(CD2-Myb/en)5Kmw/Lrfn2+
(involves: C57BL/10 * CBA)
|
decreased T cell proliferation
|
J:126456
|
Lrfn2Tg(CD2-Myb/en)5Kmw/Lrfn2Tg(CD2-Myb/en)5Kmw
(involves: C57BL/10 * CBA)
|
decreased T cell proliferation
|
J:126456
|
LrgukKaos/LrgukKaos
(involves: C57BL/6 * CBA)
|
abnormal acrosome morphology
|
J:222840
|
abnormal manchette morphology
|
J:222840
|
abnormal manchette perinuclear ring morphology
|
J:222840
|
abnormal sperm axoneme morphology
|
J:222840
|
abnormal sperm head morphology
|
J:222840
|
abnormal spermatid morphology
|
J:222840
|
absent sperm flagellum
|
J:222840
|
asthenozoospermia
|
J:222840
|
decreased male germ cell number
|
J:222840
|
detached acrosome
|
J:222840
|
oligozoospermia
|
J:222840
|
short sperm flagellum
|
J:222840
|
spontaneous chromosome breakage
|
J:222840
|
teratozoospermia
|
J:222840
|
Lrig1tm1Ita/Lrig1tm1Ita
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:77286
|
increased keratinocyte proliferation
|
J:77286
|
Lrig2tm1.1Hhed/Lrig2tm1.1Hhed
(involves: 129 * C57BL/6 * FVB/N)
|
cellular phenotype
|
J:205929
|
Lrp1tm2Her/Lrp1tm2Her Tg(Fabp4-cre)1Rev/0
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased skeletal muscle cell glucose uptake
|
J:127398
|
Lrp1tm2Her/Lrp1tm2Her Tg(Tagln-cre)1Her/0
(involves: 129S7/SvEvBrd * C57BL/6 * SJL)
|
cardiac interstitial fibrosis
|
J:209752
|
Lrp2tm1Her/Lrp2tm1Her
(involves: 129S7/SvEvBrd)
|
increased apoptosis
|
J:34835
|
Lrp5tm1.2Vari/Lrp5tm1.2Vari Lrp6tm1.1Vari/Lrp6tm1.1Vari Twist2tm1(cre)Dor/Twist2+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoblast differentiation
|
J:178499
|
Lrp5tm1Grw/Lrp5tm1Grw
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoblast physiology
|
J:104382
|
Lrp5tm1Kry/Lrp5+
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J))
|
abnormal osteoblast physiology
|
J:75973
|
Lrp5tm1Kry/Lrp5tm1Kry
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J))
|
abnormal osteoblast physiology
|
J:75973
|
decreased apoptosis
|
J:75973
|
Lrp5tm2Kry/Lrp5tm2Kry Tg(Vil1-cre)20Syr/0
(involves: C57BL/6 * DBA/2)
|
decreased osteoblast proliferation
|
J:146078
|
Lrp8tm1Her/Lrp8tm1Her
(involves: 129S6/SvEvTac)
|
abnormal cell death
|
J:117956
|
abnormal neuronal migration
|
J:117956
|
abnormal sperm flagellum morphology
|
J:84102
|
abnormal sperm midpiece morphology
|
J:84102
|
abnormal sperm mitochondrial sheath morphology
|
J:84102
|
asthenozoospermia
|
J:84102
|
coiled sperm flagellum
|
J:84102
|
hairpin sperm flagellum
|
J:84102
|
kinked sperm flagellum
|
J:84102
|
Lrp8tm1Her/Lrp8tm1Her Vldlrtm1Her/Vldlrtm1Her
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J)
|
abnormal neuronal precursor cell migration
|
J:121846
|
Lrp8tm2.1Her/Lrp8tm2.1Her
(involves: 129S6/SvEvTac)
|
abnormal cell death
|
J:117956
|
Lrp8tm4Her/Lrp8tm4Her
(Not Specified)
|
abnormal neuronal migration
|
J:117956
|
Lrp8tm5Her/Lrp8tm5Her
(Not Specified)
|
abnormal neuronal migration
|
J:117956
|
Lrp12em1Gpt/Lrp12em1Gpt Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * C57BL/6JGpt * DBA/2)
|
enhanced leukocyte migration
|
J:338432
|
increased cell migration
|
J:338432
|
Lrpap1tm1Her/Lrpap1tm1Her
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal cell physiology
|
J:43736
|
Lrpprctm1.1Lrsn/Lrpprctm1.1Lrsn Tg(Ckmm-cre)5Khn/0
(involves: 129S1/Sv * 129X1/SvJ * FVB)
|
abnormal mitochondrial physiology
|
J:187800
|
increased mitochondrial DNA content
|
J:187800
|
increased mitochondrial size
|
J:187800
|
Lrrc8atm1.1Geha/Lrrc8atm1.1Geha
(B6.129S1(Cg)-Lrrc8atm1.1Geha)
|
abnormal thymus apoptosis
|
J:211308
|
decreased T cell proliferation
|
J:211308
|
increased thymocyte apoptosis
|
J:211308
|
Lrrc23em1Mngx/Lrrc23em1Mngx
(involves: C57BL/6 * DBA/2)
|
abnormal sperm axoneme morphology
|
J:320661
|
abnormal sperm radial spoke morphology
|
J:320661
|
asthenozoospermia
|
J:320661
|
decreased sperm progressive motility
|
J:320661
|
Lrrc23em1Mngx/Lrrc23em1Mngx Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
(involves: C57BL/6 * DBA/2)
|
asthenozoospermia
|
J:320661
|
Lrrc23em2Mngx/Lrrc23em2Mngx
(involves: C57BL/6 * DBA/2)
|
abnormal sperm radial spoke morphology
|
J:320661
|
asthenozoospermia
|
J:320661
|
decreased sperm progressive motility
|
J:320661
|
Lrrc46em1Cya/Lrrc46em1Cya
(C57BL/6N-Lrrc46em1Cya)
|
abnormal manchette morphology
|
J:330199
|
abnormal outer dense fiber morphology
|
J:330199
|
abnormal sperm axoneme morphology
|
J:330199
|
abnormal sperm flagellum morphology
|
J:330199
|
abnormal sperm head morphology
|
J:330199
|
abnormal sperm mitochondrial sheath morphology
|
J:330199
|
absent sperm axonemal central pair
|
J:330199
|
absent sperm fibrous sheath
|
J:330199
|
absent sperm flagellum
|
J:330199
|
coiled sperm flagellum
|
J:330199
|
detached acrosome
|
J:330199
|
elongated manchette
|
J:330199
|
immotile sperm
|
J:330199
|
increased sperm mitochondrial size
|
J:330199
|
oligozoospermia
|
J:330199
|
short sperm flagellum
|
J:330199
|
Lrriq1em1Ysato/Lrriq1em1Ysato
(C57BL/6N-Lrriq1em1Ysato)
|
asthenozoospermia
|
J:338085
|
increased male germ cell apoptosis
|
J:338085
|
Lrrk2tm1.1Cai/Lrrk2tm1.1Cai
(involves: 129X1/SvJ * C57BL/6)
|
abnormal Golgi vesicle transport
|
J:314451
|
abnormal vesicle-mediated transport
|
J:314451
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:314451
|
Lrrk2tm1.1Hlme/Lrrk2+
(involves: C57BL/6 * C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:223350
|
abnormal mitochondrial morphology
|
J:223350
|
abnormal mitochondrial shape
|
J:223350
|
Lrrk2tm1.1Hlme/Lrrk2tm1.1Hlme
(involves: C57BL/6 * C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:223350
|
abnormal mitochondrial fission
|
J:223350
|
abnormal mitochondrial morphology
|
J:223350
|
abnormal mitochondrial shape
|
J:223350
|
decreased mitochondrial number
|
J:223350
|
dilated mitochondrion
|
J:223350
|
Lrrk2tm1.1Shn/Lrrk2tm1.1Shn
(involves: 129 * C57BL/6)
|
abnormal Golgi vesicle transport
|
J:314451
|
Lrrk2tm1Mjfa/Lrrk2tm1Mjfa
(involves: C57BL/6)
|
abnormal axon extension
|
J:172418
|
Lrrk2tm2.1Shn/Lrrk2tm2.1Shn
(involves: 129 * C57BL/6)
|
abnormal autophagy
|
J:160542
|
increased kidney apoptosis
|
J:160542
|
increased renal glomerulus apoptosis
|
J:160542
|
increased renal tubule apoptosis
|
J:160542
|
Lsm14btm1a(KOMP)Mbp/Lsm14btm1a(KOMP)Mbp
(involves: C57BL/6J * C57BL/6N)
|
abnormal female meiosis
|
J:337864
|
abnormal meiotic spindle assembly checkpoint
|
J:337864
|
abnormal oocyte morphology
|
J:337864
|
abnormal oogenesis
|
J:337864
|
abnormal translation
|
J:337864
|
impaired polar body extrusion
|
J:337864
|
oocyte degeneration
|
J:337864
|
Lsp1tm1Jejb/Lsp1tm1Jejb
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cellular extravasation
|
J:96022
|
impaired neutrophil chemotaxis
|
J:68128
|
Lspcq1PWK/PhJ/Lspcq1PWK/PhJ
(involves: LEWES/EiJ * PWK/PhJ)
|
oligozoospermia
|
J:139578
|
Lta/Tnftm1Eug/Lta/Tnftm1Eug
(B6.129-Lta/Tnftm1Eug)
|
impaired macrophage phagocytosis
|
J:115034
|
Lta/Tnftm1Eug/Lta/Tnftm1Eug
(B6.129-Lta/Tnftm1Eug)
|
impaired macrophage phagocytosis
|
J:115034
|
Ltb4r1tm1Adl/Ltb4r1tm1Adl
(involves: 129S4/SvJae * C57BL/6)
|
abnormal leukocyte adhesion
|
J:63873
|
abnormal leukocyte migration
|
J:63873
|
impaired neutrophil chemotaxis
|
J:63873
|
Ltb4r1tm1Bodd/Ltb4r1tm1Bodd
(either: (involves: 129S4/SvJaeSor * BALB/c ) or (involves: 129S4/SvJaeSor * C57BL/6))
|
impaired neutrophil chemotaxis
|
J:163271
|
Ltb4r1tm1Tksh/Ltb4r1tm1Tksh
(B6.Cg-Ltb4r1tm1Tksh)
|
decreased cell proliferation
|
J:118995
|
Ltbp4Gt(U3Cre)1Vmel/Ltbp4Gt(U3Cre)1Vmel
(B6.129S2-Ltbp4Gt(U3Cre)1Vmel)
|
abnormal cell physiology
|
J:78819
|
abnormal intestinal goblet cell morphology
|
J:78819
|
Ltftm1.2Smoc/Ltftm1.2Smoc
(involves: 129 * C57BL/6J)
|
decreased apoptosis
|
J:219007
|
increased cell proliferation
|
J:219007
|
Lumtm1Chak/Lumtm1Chak
(involves: 129S/Sv * CD-1)
|
abnormal apoptosis
|
J:89489
|
decreased fibroblast apoptosis
|
J:89489
|
increased fibroblast proliferation
|
J:89489
|
Luzp1tm1Acch/Luzp1tm1Acch
(B6.129P2-Luzp1tm1Acch)
|
increased hindbrain apoptosis
|
J:141306
|
Lvs/Lvs+
(involves: BALB/cByJ * C57BL/6J * SJL/J)
|
teratozoospermia
|
J:2977
|
Lvs/Lvs+
(involves: BALB/cByJ * C57BL/6J * FVB/N * SJL/J)
|
teratozoospermia
|
J:2977
|
Ly6atm1Pmf/Ly6atm1Pmf
(B6.129P2-Ly6atm1Pmf)
|
abnormal T cell proliferation
|
J:42594
|
Ly6atm1Pmf/Ly6atm1Pmf
(C.129P2-Ly6atm1Pmf)
|
abnormal osteoblast differentiation
|
J:83409
|
abnormal osteoblast physiology
|
J:83409
|
abnormal osteoclast differentiation
|
J:83409
|
Ly6ktm1Osb/Ly6ktm1Osb
(involves: 129S2/SvPas * C57BL/6NSlc)
|
impaired sperm migration in female genital tract
|
J:210341
|
Ly9tm1Mckn/Ly9tm1Mckn
(involves: 129/Sv * C57BL/6)
|
decreased T cell proliferation
|
J:105482
|
Ly86tm1Kmiy/Ly86tm1Kmiy
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:109720
|
Ly96m1Btlr/Ly96m1Btlr
(C57BL/6J-Ly96m1Btlr)
|
decreased macrophage apoptosis
|
J:265259
|
Ly96tm1Kmiy/Ly96tm1Kmiy
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:92494
|
LyarGt(RRG292)Byg/Lyar+
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased fibroblast proliferation
|
J:263530
|
LyarGt(RRG292)Byg/LyarGt(RRG292)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased fibroblast proliferation
|
J:263530
|
Lyntm1Sor/Lyntm1Sor
(involves: 129S4/SvJae)
|
increased B cell proliferation
|
J:42037
|
Lyntm1Sor/Lyntm1Sor
(involves: 129S4/SvJaeSor)
|
increased B cell proliferation
|
J:146161
|
mesangial cell interposition
|
J:146161
|
Lyntm1Sor/Lyntm1Sor
(involves: 129S4/SvJaeSor * C57BL/6)
|
increased B cell proliferation
|
J:71174
|
Lyntm1Tya/Lyntm1Tya
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:29751
|
Lynweeb/Lynweeb
(C57BL/6-Lynweeb)
|
increased B cell proliferation
|
J:146161
|
mesangial cell interposition
|
J:146161
|
Lynx1tm1Htz/Lynx1tm1Htz
(involves: 129X1/SvJ * C57BL/6J)
|
increased susceptibility to neuronal excitotoxicity
|
J:122965
|
Lypd4em1Eyx/Lypd4em1Eyx
(involves: C57BL/6N)
|
impaired sperm migration in female genital tract
|
J:294725
|
Lypla1tm1Sem/Lypla1tm1Sem Tg(Tek-cre)12Flv/0
(B6(Cg)-Lypla1tm1Sem Tg(Tek-cre)12Flv)
|
abnormal vascular endothelial cell adhesion
|
J:302677
|
Lyr3BALB/cHeA/Lyr3BALB/cHeA
(involves: BALB/cHeA * STS/A)
|
increased cellular sensitivity to X-ray irradiation
|
J:21861
|
Lysetem1Janc/Lysetem1Janc
(C57BL/6J-Tmem251em1Janc)
|
abnormal lysosome morphology
|
J:330704
|
Lysetem1Janc/Lysetem2Janc
(C57BL/6J-Tmem251em1Janc Tmem251em2Janc)
|
abnormal lysosome morphology
|
J:330704
|
Lysetem2Janc/Lysetem2Janc
(C57BL/6J-Tmem251em2Janc)
|
abnormal lysosome morphology
|
J:330704
|
Lystbg-5Btlr/Lyst+
(C57BL/6J-Lystbg-5Btlr)
|
impaired macrophage phagocytosis
|
J:217864
|
Lystbg-5Btlr/Lystbg-5Btlr
(C57BL/6J-Lystbg-5Btlr)
|
impaired macrophage phagocytosis
|
J:217864
|
Lystbg-J/Lystbg-J
(C57BL/6J-Lystbg-J/J)
|
decreased lysosomal enzyme secretion
|
J:7327
|
decreased platelet ATP level
|
J:7327
|
Lystbg-Lac/Lystbg-Lac
(CBA/CaLac-Lystbg-Lac)
|
abnormal lysosome morphology
|
J:29745
|
Lystbg/Lystbg
(B6.C3Rl-Lystbg)
|
abnormal lysosome morphology
|
J:5338,
J:5514
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:5590
|
decreased lysosomal enzyme secretion
|
J:5590
|
lysosomal protein accumulation
|
J:5590
|
Lystbg/Lystbg
(B6.C3Rl-Lystbg/J)
|
abnormal lysosome morphology
|
J:6629
|
abnormal lysosome physiology
|
J:6801
|
Lyve1tm1.1(EGFP/cre)Cys/Lyve1+ Sphk1tm2Cgh/Sphk1tm2Cgh Sphk2tm1.1Cgh/Sphk2tm1.1Cgh
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
abnormal leukocyte migration
|
J:156826
|
Lyz2tm1(cre)Ifo/Lyz2+ Selenowtm1c(EUCOMM)Wtsi/Selenowtm1c(EUCOMM)Wtsi
(B6.Cg-Selenowtm1c(EUCOMM)Wtsi Lyz2tm1(cre)Ifo)
|
abnormal osteoclast differentiation
|
J:317012
|
Lyz2tm1(cre)Ifo/Lyz2tm1(cre)Ifo Nrrostm1Wouy/Nrrostm1Wouy
(involves: 129P2/OlaHsd)
|
abnormal cellular extravasation
|
J:209569
|
oxidative stress
|
J:209569
|
Lztfl1tm1.3Zpl/Lztfl1tm1.3Zpl
(involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N)
|
decreased embryonic cilium length
|
J:287261
|
Lztfl1tm1e(KOMP)Wtsi/Lztfl1tm1e(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal elongated spermatid morphology
|
J:307611
|
abnormal sperm end piece morphology
|
J:307611
|
abnormal sperm fibrous sheath morphology
|
J:307611
|
abnormal sperm flagellum morphology
|
J:307611
|
abnormal sperm flagellum thickness
|
J:307611
|
abnormal sperm head morphology
|
J:307611
|
abnormal sperm nucleus morphology
|
J:307611
|
asthenozoospermia
|
J:307611
|
oligozoospermia
|
J:307611
|
short sperm flagellum
|
J:307611
|
teratozoospermia
|
J:307611
|
Lztr1tm1a(EUCOMM)Wtsi/Lztr1+
(involves: C57BL/6N)
|
increased cell proliferation
|
J:268690
|
Lzts1tm1Cro/Lzts1tm1Cro
(involves: 129 * C57BL/6J)
|
abnormal cell cycle
|
J:119989
|
abnormal fibroblast physiology
|
J:119989
|
decreased fibroblast proliferation
|
J:119989
|
increased fibroblast apoptosis
|
J:119989
|
M1apGt(RRO290)Byg/M1apGt(RRO290)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:194507
|
abnormal male germ cell apoptosis
|
J:194507
|
abnormal male germ cell morphology
|
J:194507
|
abnormal male meiosis
|
J:194507
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:194507
|
arrest of male meiosis
|
J:194507
|
globozoospermia
|
J:194507
|
oligozoospermia
|
J:194507
|
X/m1Nish
(involves: C57BL/6N)
|
decreased T cell proliferation
|
J:204833
|
m4Sapc/m4Sapc
(C57BL/6J-m4Sapc)
|
abnormal axon fasciculation
|
J:163657
|
M6prtm1Hlk/M6prtm1Hlk
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased lysosomal enzyme secretion
|
J:111016
|
lysosomal protein accumulation
|
J:111016
|
m1078Lja/m1078Lja
(involves: C57BL/6J * DBA)
|
decreased male germ cell number
|
J:179895
|
Macf1tm1Efu/Macf1tm1Efu Tg(KRT14-cre)1Efu/0
(involves: 129)
|
decreased keratinocyte migration
|
J:143595
|
increased keratinocyte adhesion
|
J:143595
|
Macf1tm1Efu/Macf1tm1Efu Tg(Six3-cre)69Frty/0
(involves: 129 * C57BL/6 * DBA/2)
|
abnormal photoreceptor connecting cilium morphology
|
J:240903
|
Macf1tm2.1Liem/Macf1tm2.2Liem Tg(Nes-cre)1Kln/0
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL)
|
abnormal neuronal migration
|
J:164146
|
Macroh2a1tm1.1Oxbo/Macroh2a1tm1.1Oxbo
(B6.Cg-Macroh2a1tm1.1Oxbo)
|
increased sensitivity to induced cell death
|
J:293382
|
Mad1l1tm1.1Ktj/Mad1l1+
(involves: BALB/c * C57BL/6J)
|
abnormal cell physiology
|
J:117337
|
abnormal chromosome number
|
J:117337
|
abnormal mitotic spindle assembly checkpoint
|
J:117337
|
aneuploidy
|
J:117337
|
Mad1l1tm1.1Ktj/Mad1l1+ Mad2l1tm1Sorg/Mad2l1+
(involves: 129S2/SvPas * BALB/c * C57BL/6J)
|
abnormal cell physiology
|
J:117337
|
abnormal chromosome number
|
J:117337
|
abnormal mitotic spindle assembly checkpoint
|
J:117337
|
aneuploidy
|
J:117337
|
Mad2l1tm1Sorg/Mad2l1+
(involves: 129S2/SvPas * C57BL/6)
|
cellular phenotype
|
J:62829
|
chromosome breakage
|
J:67456
|
Mad2l1tm1Sorg/Mad2l1+
(involves: 129S2/SvPas)
|
abnormal cell physiology
|
J:117337
|
abnormal chromosome number
|
J:117337
|
aneuploidy
|
J:117337,
J:105717
|
Mad2l1tm1Sorg/Mad2l1+ Usp44tm1.2Pjgl/Usp44tm1.2Pjgl
(involves: 129S2/SvPas * 129S4/SvJae * 129S7/SvEvBrd)
|
chromosomal instability
|
J:193965
|
Mad2l1tm1Sorg/Mad2l1tm1Sorg
(involves: 129S2/SvPas * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:62829
|
abnormal mitosis
|
J:62829
|
abnormal mitotic spindle assembly checkpoint
|
J:62829
|
absent inner cell mass proliferation
|
J:62829
|
increased embryonic tissue cell apoptosis
|
J:62829
|
Mad2l1tm2Sorg/Mad2l1tm2Sorg Tg(KRT14-cre)1Amc/?
(Not Specified)
|
aneuploidy
|
J:194539
|
Mad2l1bptm1.1Itl/Mad2l1bptm1.1Itl Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NTac)
|
abnormal endocytosis
|
J:234643
|
aneuploidy
|
J:234643
|
Mad2l1bptm1.2Itl/Mad2l1bptm1.2Itl
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NTac)
|
abnormal mitosis
|
J:234643
|
aneuploidy
|
J:234643
|
decreased adipocyte glucose uptake
|
J:234643
|
decreased fibroblast proliferation
|
J:234643
|
increased fibroblast apoptosis
|
J:234643
|
increased mitotic index
|
J:234643
|
polyploidy
|
J:234643
|
Mad2l2repro22/Mad2l2repro22
(involves: C3HeB/FeJ * C57BL/6J)
|
azoospermia
|
J:92463
|
decreased male germ cell number
|
J:92463
|
decreased oocyte number
|
J:92463
|
Mad2l2repro22/Mad2l2repro22
(C3.B6(Cg)-Mad2l2repro22)
|
absent germ cells
|
J:209515
|
cellular phenotype
|
J:209515
|
decreased cell proliferation
|
J:209515
|
decreased primordial germ cell number
|
J:209515
|
increased enterocyte apoptosis
|
J:209515
|
Mad2l2tm1.1Mpz/Mad2l2tm1.1Mpz
(involves: 129S2/SvPas * BALB/cJ)
|
abnormal cell cycle
|
J:223048
|
abnormal epigenetic regulation of gene expression
|
J:223048
|
abnormal primordial germ cell migration
|
J:223048
|
abnormal primordial germ cell morphology
|
J:223048
|
absent germ cells
|
J:223048
|
absent primordial germ cells
|
J:223048
|
decreased primordial germ cell number
|
J:223048
|
increased primordial germ cell apoptosis
|
J:223048
|
Mad2l2tm1Mpz/Mad2l2tm1Mpz Tg(Prdm1-cre)1Masu/0
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
abnormal primordial germ cell apoptosis
|
J:223048
|
Mad2l2tm1Ymu/Mad2l2tm1Ymu
(involves: 129 * C57BL/6J)
|
abnormal double-strand DNA break repair
|
J:198275
|
abnormal oogenesis
|
J:198275
|
absent primordial germ cells
|
J:198275
|
azoospermia
|
J:198275
|
decreased primordial germ cell number
|
J:198275
|
increased forebrain apoptosis
|
J:198275
|
increased primordial germ cell apoptosis
|
J:198275
|
Maeltm1Bort/Maeltm1Bort
(B6.129S4-Maeltm1Bort)
|
abnormal DNA methylation during gametogenesis
|
J:140402
|
abnormal male meiosis
|
J:140402
|
abnormal spermatocyte morphology
|
J:140402
|
increased male germ cell apoptosis
|
J:140402
|
Maeltm1Bort/Maeltm1Bort Spo11tm1Rdco/Spo11tm1Rdco
(involves: 129 * C57BL/6)
|
abnormal male meiosis
|
J:140402
|
Mafbkr/Mafbkr
(CBA.Cg-Mafbkr)
|
abnormal cell cycle
|
J:5392
|
abnormal cell cycle checkpoint function
|
J:5392
|
Mafbtm1Jeng/Mafbtm1Jeng
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased renal tubule apoptosis
|
J:111415
|
Mafgtm1Jeng/Mafgtm1Jeng
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal megakaryocyte differentiation
|
J:78982
|
Mafgtm1Jeng/Mafgtm1Jeng
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal megakaryocyte differentiation
|
J:78982
|
Mafgtm1Jeng/Mafgtm1Jeng Mafktm1Jeng/Mafk+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal megakaryocyte differentiation
|
J:61142
|
Magtm1Rod/Magtm1Rod
(involves: 129S1/Sv * 129X1/SvJ)
|
increased B cell proliferation
|
J:217719
|
Mageb5bem1JbmuDel(XMageb5)1Jbmu/Y
(B6(SJL)-Mageb5bem1Jbmu Del(XMageb5)1Jbmu/Jbmu)
|
teratozoospermia
|
J:334464
|
Mageb5bem2JbmuDel(XMageb5)1Jbmu/Y
(B6(SJL)-Mageb5bem2Jbmu Del(XMageb5)1Jbmu/Jbmu)
|
teratozoospermia
|
J:334464
|
Maged1tm1.1Urfm/Maged1tm1.1Urfm
(B6.129P2-Maged1tm1.1Urfm)
|
decreased neuron apoptosis
|
J:157604
|
Magel2tm1Stw/Magel2+
(C57BL/6-Magel2tm1Stw)
|
maternal imprinting
|
J:144836
|
Magel2tm1Stw/Magel2tm1Stw
(C57BL/6-Magel2tm1Stw)
|
maternal imprinting
|
J:125637
|
Magel2tm1Stw/Magel2tm1Stw
(C57BL/6-Magel2tm1Stw/J)
|
abnormal autophagy
|
J:233299
|
Magi2tm1Key/Magi2tm1Key
(involves: 129S4/SvJae)
|
abnormal endoplasmic reticulum morphology
|
J:213553
|
MagohMos2/Magoh+
(involves: BALB/cJ * C57BL/6J)
|
abnormal mitotic spindle morphology
|
J:159625
|
abnormal neuron apoptosis
|
J:159625
|
abnormal neuron proliferation
|
J:159625
|
increased brain apoptosis
|
J:240595
|
Magt1Gt(IST13422E1)Tigm/Y
(involves: C57BL/6N)
|
increased B cell proliferation
|
J:260923
|
Majinem1Smtb/Majinem1Smtb
(C57BL/6NSlc-Majinem1Smtb/Smtb)
|
absent oocytes
|
J:308859
|
arrest of male meiosis
|
J:308859
|
azoospermia
|
J:308859
|
Majinem2Smtb/Majinem2Smtb
(C57BL/6NSlc-Majinem2Smtb/Smtb)
|
absent oocytes
|
J:308859
|
arrest of male meiosis
|
J:308859
|
azoospermia
|
J:308859
|
Maktm1Yshk/Maktm1Yshk
(B6.Cg-Maktm1Yshk)
|
asthenozoospermia
|
J:76245
|
Malat1tm1.2Dlsp/Malat1tm1.2Dlsp
(B6J.Cg-Malat1tm1.2Dlsp)
|
increased brain apoptosis
|
J:239375
|
Malt1tm1Mak/Malt1tm1Mak
(involves: 129P2/OlaHsd)
|
decreased T cell proliferation
|
J:109545
|
Malt1tm1Vmd/Malt1tm1Vmd
(involves: C57BL/6N)
|
abnormal T cell proliferation
|
J:86770
|
Maml1tm1Mkit/Maml1tm1Mkit Maml3tm1Mkit/Maml3tm1Mkit
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuron proliferation
|
J:178680
|
Mamstrtm1.2Eno/Mamstrtm1.2Eno Mrtfatm1Eno/Mrtfatm1Eno
(involves: 129 * C57BL/6)
|
abnormal skeletal muscle satellite cell proliferation
|
J:179880
|
Man2a1tm1Jxm/Man2a1tm1Jxm Rag1tm1Mom/Rag1tm1Mom
(B6.129-Rag1tm1Mom Man2a1tm1Jxm)
|
increased mesangial cell apoptosis
|
J:124348
|
Man2a2tm1Mfu/Man2a2tm1Mfu
(involves: 129S1/Sv * 129X1/SvJ)
|
oligozoospermia
|
J:73658,
J:80105
|
Man2b1tm1Psa/Man2b1tm1Psa
(involves: 129 * C57BL/6J)
|
abnormal lysosome morphology
|
J:56659,
J:99812
|
Manbatm1Khf/Manbatm1Khf
(B6.129-Manbatm1Khf)
|
abnormal lysosome physiology
|
J:105427
|
Manftm1a(KOMP)Wtsi/Manftm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal neuronal migration
|
J:255942
|
abnormal translation
|
J:255942
|
Manftm1a(KOMP)Wtsi/Manftm1a(KOMP)Wtsi
(involves: C57BL/6 * C57BL/6N * ICR)
|
abnormal pancreatic beta cell differentiation
|
J:211812
|
abnormal translation
|
J:211812
|
increased pancreas apoptosis
|
J:211812
|
Maobtm1Shih/Maobtm1Shih
(either: (involves: 129S/SvEv) or (involves: 129S4/SvJae))
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:43648
|
Map1atm1.2(KOMP)Mbp/Map1atm1.2(KOMP)Mbp
(involves: 129S4/SvJaeSor * C57BL/6N * C57BL/6NJ)
|
abnormal microtubule cytoskeleton morphology
|
J:220153
|
Map1btm1Prop/Map1btm1Prop
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal axon extension
|
J:97265
|
Map1lc3btm1Mrab/Map1lc3btm1Mrab
(involves: 129P2/OlaHsd)
|
abnormal intestinal goblet cell morphology
|
J:206181
|
Map1stm1.1Lliu/Map1stm1.1Lliu
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal autophagosome formation
|
J:170757
|
Map1stm1.1Lliu/Map1stm1.1Lliu Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6NCrj)
|
abnormal autophagy
|
J:170757
|
Map2repro4/Map2repro4
(B6;C3Fe-Maprepro4/J)
|
abnormal germ cell morphology
|
J:92463
|
arrest of male meiosis
|
J:92463
|
azoospermia
|
J:92463
|
Map2repro4/Map2repro4
(C3.B6-Map2repro4)
|
abnormal spermatocyte morphology
|
J:205107
|
arrest of male meiosis
|
J:205107
|
decreased round spermatid number
|
J:205107
|
Map2k1Gt(ROSABetageo)J2Chrn/Map2k1Gt(ROSABetageo)J2Chrn
(involves: 129/Sv * 129S/SvEv * C57BL/6J * SJL)
|
abnormal cell migration
|
J:54197
|
abnormal vascular endothelial cell migration
|
J:54197
|
Map2k1tm1Chrn/Map2k1tm1Chrn Map2k2tm1Chrn/Map2k2tm1Chrn Tg(KRT14-cre)1Efu/?
(involves: 129/Sv * C57BL/6J * SJL)
|
increased keratinocyte apoptosis
|
J:122484
|
Map2k3tm1Flv/Map2k3tm1Flv
(involves: 129S1/Sv)
|
decreased T cell apoptosis
|
J:85266
|
Map2k4tm1Ctr/Map2k4tm1Ctr Map2k7tm1Rjd/Map2k7tm1Rjd Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * CBA)
|
decreased neuron apoptosis
|
J:178060
|
Map2k4tm1Ctr/Map2k4tm1Ctr Tg(Nes-cre)1Kln/?
(involves: C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:129038
|
Map2k4tm1Lizon/Map2k4tm1Lizon
(involves: 129S1/Sv)
|
increased hepatocyte apoptosis
|
J:48772
|
Map2k5tm1Ctr/Map2k5tm1Ctr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:95388
|
increased apoptosis
|
J:95388
|
Map2k6tm1Flv/Map2k6tm1Flv
(involves: 129S1/Sv)
|
abnormal thymocyte apoptosis
|
J:85266
|
decreased cellular sensitivity to gamma-irradiation
|
J:85266
|
Map2k6tm1Ina/Map2k6tm1Ina
(involves: 129P2/OlaHsd)
|
decreased apoptosis
|
J:100093
|
Map2k6tm1Ina/Map2k6tm1Ina Tg(TcraH-Y,TcrbH-Y)71Vbo/0
(involves: 129P2/OlaHsd * C57BL/6J * DBA/2J)
|
decreased apoptosis
|
J:100093
|
Map2k6tm1Ina/Map2k6tm1Ina Tg(TcrLCMV)327Sdz/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
decreased apoptosis
|
J:100093
|
Map3k1tm1Glj/Map3k1tm1Glj
(involves: 129S/SvEv)
|
impaired fibroblast cell migration
|
J:62909
|
increased cardiomyocyte apoptosis
|
J:78068
|
Map3k1tm1Yxia/Map3k1tm1Yxia
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
increased retina apoptosis
|
J:176244
|
Map3k2tm1Bisu/Map3k2tm1Bisu
(Not Specified)
|
increased T cell proliferation
|
J:78072
|
Map3k3tm1Bisu/Map3k3tm2Bisu Tg(Lck-cre)548Jxm/0
(involves: C57BL/6 * CBA)
|
abnormal T cell proliferation
|
J:145923
|
Map3k3tm1Kuro/Map3k3tm1Kuro Tg(Lck-cre)1Jtak/0
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:147103
|
Map3k4tm1Glj/Map3k4tm1Glj
(involves: 129S6/SvEvTac * C57BL/6)
|
asthenozoospermia
|
J:101350
|
oligozoospermia
|
J:101350
|
Map3k5tm1Hijo/Map3k5tm1Hijo
(involves: 129S4/SvJae * C57BL/6J)
|
decreased sensitivity to induced cell death
|
J:88612
|
Map3k6tm1Hijo/Map3k6tm1Hijo
(B6.129P2-Map3k6tm1Hijo)
|
decreased keratinocyte apoptosis
|
J:148044
|
Map3k7Gt(XB444)Byg/Map3k7Gt(XB444)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal vascular regression
|
J:107401
|
Map3k7tm1.1Aki/Map3k7tm1.1Aki
(involves: 129P2/OlaHsd * C57BL/6)
|
absent fibroblast proliferation
|
J:112597
|
Map3k7tm1Aki/Map3k7tm1Aki Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
increased hepatocyte proliferation
|
J:160521
|
Map3k7tm1Aki/Map3k7tm1Aki Tg(Alb1-cre)7Gsc/0
(involves: 129P2/OlaHsd * FVB/N)
|
increased hepatocyte apoptosis
|
J:160521
|
increased hepatocyte proliferation
|
J:160521
|
Map3k7tm1Aki/Map3k7tm1Aki Tg(Lck-cre)1Jtak/0
(involves: 129P2/OlaHsd)
|
abnormal intestinal goblet cell morphology
|
J:112837
|
decreased T cell proliferation
|
J:112837
|
Map3k7tm1Aki/Map3k7tm1Aki Tg(Tek-cre)12Flv/0
(involves: 129P2/OlaHsd * C3H * C57BL/6)
|
increased apoptosis
|
J:191285
|
Map3k7tm1Aki/Map3k7tm1Aki Tnfrsf1atm1Mak/Tnfrsf1atm1Mak Tg(Tek-cre)12Flv/0
(involves: 129P2/OlaHsd * 129S2/SvPas * C3H * C57BL/6)
|
cellular phenotype
|
J:191285
|
Map3k7tm1Zjc/Map3k7tm1Zjc Tg(Lck-cre)548Jxm/0
(involves: 129S7/SvEvBrd * C57BL/6 * CBA)
|
increased thymocyte apoptosis
|
J:111794
|
Map3k8tm1.1Gkl/Map3k8tm1.1Gkl Tg(Col6a1-cre)1Gkl/0
(involves: C57BL/6 * CBA * FVB/N)
|
abnormal enterocyte proliferation
|
J:193546
|
decreased enterocyte apoptosis
|
J:193546
|
Map3k8tm1.2Gkl/Map3k8tm1.2Gkl
(involves: 129 * C57BL/6J * FVB/N)
|
abnormal enterocyte proliferation
|
J:193546
|
decreased enterocyte apoptosis
|
J:193546
|
Map3k8tm1Tmat/Map3k8tm1Tmat
(involves: 129S/SvEv * C57BL/6)
|
increased T cell proliferation
|
J:92844
|
Map3k11tm1Rjd/Map3k11tm1Rjd
(involves: 129S6/SvEvTac * C57BL/6J)
|
cellular phenotype
|
J:97631
|
Map3k12tm1.1Lewc/Map3k12tm1.1Lewc
(Not Specified)
|
abnormal neuron differentiation
|
J:176956
|
decreased neuron apoptosis
|
J:176956
|
Map3k12tm1Lbh/Map3k12tm1Lbh
(Not Specified)
|
abnormal axon extension
|
J:236918
|
abnormal cell physiology
|
J:236918
|
Map3k12tm1Shir/Map3k12tm1Shir
(B6.Cg-Mapk12tm1Shir)
|
decreased neuronal migration
|
J:115575
|
Map3k13tm1a(KOMP)Wtsi/Map3k13tm1a(KOMP)Wtsi
(C57BL/6N-Map3k13tm1a(KOMP)Wtsi)
|
abnormal axon extension
|
J:236918
|
abnormal cell physiology
|
J:236918
|
Map3k14aly/Map3k14aly
(involves: C57BL/6J)
|
abnormal intestinal goblet cell morphology
|
J:135748
|
Map3k15tm1Hijo/Y
(involves: C57BL/6 * ICR)
|
abnormal cell physiology
|
J:221240
|
Map4k1tm1Tht/Map4k1tm1Tht
(involves: 129S7/SvEvBrd)
|
increased T cell proliferation
|
J:116613
|
Map4k3Gt(RRO270)Byg/Map4k3Gt(RRO270)Byg
(involves: 129P2/OlaHsd)
|
decreased T cell proliferation
|
J:177642
|
Map4k5tm1Jhk/Map4k5tm1Jhk
(either: B6.129-Map4k5tm1Jhk or (involves: 129 * C57BL/6))
|
abnormal cell physiology
|
J:112134
|
Map7Gt(ROSABetageo)1Sor/Map7Gt(ROSABetageo)1Sor
(either: 129S4/SvJaeSor-Map7Gt(ROSABetageo)1Sor or (involves: 129S4/SvJaeSor * C57BL/6J))
|
abnormal spermatid morphology
|
J:62570
|
decreased germ cell number
|
J:62570
|
Map7Gt(ROSABetageo)1Sor/Map7mshi
(involves: 129S4/SvJaeSor * BALB/cBy * C57BL/6J)
|
decreased male germ cell number
|
J:148349
|
Map7mshi/Map7mshi
(involves: BALB/cBy)
|
arrest of male meiosis
|
J:37165
|
Map9tm1.2Bcgen/Map9+
(involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6)
|
abnormal centrosome morphology
|
J:299895
|
abnormal pericentriolar material morphology
|
J:299895
|
aneuploidy
|
J:299895
|
chromosomal instability
|
J:299895
|
Map9tm1.2Bcgen/Map9tm1.2Bcgen
(involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6)
|
abnormal centrosome morphology
|
J:299895
|
abnormal pericentriolar material morphology
|
J:299895
|
aneuploidy
|
J:299895
|
chromosomal instability
|
J:299895
|
Map9tm1.2Bcgen/Map9tm1.2Bcgen Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas * 129S4/SvJaeSor * BALB/cJ * C57BL/6)
|
aneuploidy
|
J:299895
|
Mapk1tm1.1Hed/Mapk1tm1.1Hed Mapk3tm1Gpg/Mapk3tm1Gpg Tg(Gdf9-icre)5092Coo/0
(involves: 129/Sv * C57BL/6 * ICR)
|
abnormal translation
|
J:245369
|
Mapk1tm1Gela/Mapk1tm1Gela Tg(GFAP-cre)25Mes/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal neuron differentiation
|
J:137882
|
Mapk1tm1Hed/Mapk1tm1Hed Mapk3tm1Gpg/Mapk3tm1Gpg Tg(Lck-cre)1Cwi/0
(involves: 129/Sv * C57BL/6 * DBA/2)
|
abnormal T cell proliferation
|
J:113280
|
Mapk1tm1Hed/Mapk1tm1Hed Tg(Lck-cre)1Cwi/0
(involves: C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:113280
|
Mapk1tm1Melo/Mapk1+
(involves: C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:127872
|
Mapk1tm1Melo/Mapk1tm1Melo Tg(CAG-EGFP)B5Nagy/0
(chimera involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * CD-1)
|
decreased fibroblast proliferation
|
J:162580
|
Mapk1tm2Melo/Mapk1tm2Melo Mapk3tm1Gpg/Mapk3tm1Gpg
(involves: 129)
|
abnormal mitosis
|
J:162580
|
early cellular replicative senescence
|
J:162580
|
increased fibroblast apoptosis
|
J:162580
|
Mapk3tm1Gpg/Mapk3tm1Gpg
(involves: 129)
|
decreased T cell proliferation
|
J:58468
|
Mapk3tm1Gpg/Mapk3tm1Gpg
(involves: 129/Sv * C57BL/6)
|
cellular phenotype
|
J:162580
|
Mapk3tm1Gpg/Mapk3tm1Gpg
(involves: 129/Sv * C57BL/6 * CD-1)
|
decreased fibroblast proliferation
|
J:162580
|
Mapk7tm1.1Ctr/Mapk7+
(involves: 129S1/Sv * 129X1/SvJ)
|
increased fibroblast apoptosis
|
J:132253
|
Mapk7tm1.1Ctr/Mapk7tm1.1Ctr
(involves: 129S1/Sv * 129X1/SvJ)
|
increased fibroblast apoptosis
|
J:132253
|
Mapk7tm1Jdl/Mapk7tm1Jdl Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal apoptosis
|
J:89215
|
Mapk8tm1Flv/Mapk8tm1Flv
(involves: 129S1/Sv * C57BL/6)
|
decreased cardiomyocyte apoptosis
|
J:102152
|
Mapk8tm1Flv/Mapk8tm1Flv
(involves: 129S1/Sv)
|
increased cardiomyocyte apoptosis
|
J:108253
|
increased T cell proliferation
|
J:51510
|
Mapk8tm1Flv/Mapk8tm1Flv Mapk9tm1.1Rjd/Mapk9tm1.1Rjd
(involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6)
|
decreased fibroblast proliferation
|
J:112737
|
decreased keratinocyte migration
|
J:112737
|
increased fibroblast apoptosis
|
J:112737
|
increased fibroblast cell migration
|
J:112737
|
Mapk8tm1Flv/Mapk8tm1Flv Mapk9tm1Flv/Mapk9tm1Flv
(involves: 129S1/Sv * 129S2/SvPas)
|
decreased hindbrain apoptosis
|
J:54653
|
increased embryonic neuroepithelium apoptosis
|
J:54653
|
increased forebrain apoptosis
|
J:54653
|
Mapk8tm1Rjd/Mapk8tm1Rjd Mapk9tm1Flv/Mapk9tm1Flv
(involves: 129S2/SvPas * C57BL/6J)
|
increased fibroblast apoptosis
|
J:131766
|
Mapk8tm1Rjd/Mapk8tm1Rjd Mapk9tm2.1Rjd/Mapk9tm2.1Rjd Lyz2tm1(cre)Ifo/Lyz2+
(B6J.Cg-Lyz2tm1(cre)Ifo Mapk9tm2.1Rjd Mapk8tm1Rjd)
|
abnormal macrophage differentiation
|
J:192551
|
decreased pancreatic beta cell proliferation
|
J:192551
|
impaired macrophage chemotaxis
|
J:192551
|
Mapk8tm1Wag/Mapk8+ Mapk9tm1Mka/Mapk9+
(involves: 129)
|
decreased T cell apoptosis
|
J:78190
|
decreased T cell proliferation
|
J:78190
|
Mapk8tm1Wag/Mapk8+ Mapk9tm1Mka/Mapk9tm1Mka
(involves: 129)
|
decreased T cell apoptosis
|
J:78190
|
decreased T cell proliferation
|
J:78190
|
Mapk8tm1Wag/Mapk8tm1Wag
(involves: 129P2/OlaHsd)
|
decreased T cell apoptosis
|
J:78190
|
decreased T cell proliferation
|
J:78190
|
Mapk8tm1Wag/Mapk8tm1Wag Mapk9tm1Mka/Mapk9+
(involves: 129)
|
decreased T cell apoptosis
|
J:78190
|
decreased T cell proliferation
|
J:78190
|
Mapk8tm1Wag/Mapk8tm1Wag Mapk9tm1Mka/Mapk9tm1Mka
(involves: 129 * C57BL/6)
|
decreased hindbrain apoptosis
|
J:58622
|
increased forebrain apoptosis
|
J:58622
|
increased hindbrain apoptosis
|
J:58622
|
Mapk8ip1tm1Rjd/Mapk8ip1tm1Rjd
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased susceptibility to neuronal excitotoxicity
|
J:77616
|
Mapk8ip1tm1Wae/Mapk8ip1tm1Wae
(either: (involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6))
|
abnormal cell death
|
J:70600
|
Mapk8ip3tm1Plhn/Mapk8ip3tm1Plhn
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal axon guidance
|
J:95744
|
abnormal neuronal migration
|
J:95744
|
Mapk8ip3tm1Rjd/Mapk8ip3tm1Rjd
(B6.129S6-Mapk8ip3tm1Rjd)
|
abnormal axon guidance
|
J:85160
|
Mapk9tm1Flv/Mapk9tm1Flv Tnftm2Gkl/Tnf+
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J)
|
increased apoptosis
|
J:108572
|
Mapk9tm1Mka/Mapk9tm1Mka
(either: (involves: 129S2/SvPas) or (involves: 129S1/Sv * 129X1/SvJ))
|
decreased T cell apoptosis
|
J:78129
|
decreased T cell proliferation
|
J:78129
|
Mapk9tm1Mka/Mapk9tm1Mka
(involves: 129/Sv * C57BL/6)
|
decreased cardiomyocyte apoptosis
|
J:102152
|
Mapk10tm1Flv/Mapk10tm1Flv
(involves: 129S1/Sv)
|
abnormal cell death
|
J:117956
|
decreased neuron apoptosis
|
J:124252
|
decreased susceptibility to neuronal excitotoxicity
|
J:43658
|
Mapk10tm1Flv/Mapk10tm1Flv
(B6.129S1-Mapk10tm1Flv)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:87428
|
Mapk10tm1Flv/Mapk10tm1Flv Mapk9tm1Flv/Mapk9tm1Flv
(B6.129S-Mapk9tm1Flv Mapk10tm1Flv)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:87428
|
Mapk11tm1Jda/Mapk11tm1Jda Mapk14tm1Jda/Mapk14tm1Jda
(involves: 129 * C57BL/6)
|
decreased T cell proliferation
|
J:165966
|
Mapk11tm1Jsca/Mapk11tm1Jsca
(involves: 129P2/OlaHsd)
|
increased fetal cardiomyocyte proliferation
|
J:176023
|
Mapk11tm1Jsca/Mapk11tm1Jsca Mapk14tm2Nbr/Mapk14tm2Nbr Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal fetal cardiomyocyte proliferation
|
J:176023
|
abnormal neuron proliferation
|
J:176023
|
increased hepatocyte apoptosis
|
J:176023
|
Mapk11tm2Lex/Mapk11tm2Lex Tg(Myog-cre)1Eno/0
(involves: 129S/SvEvBrd)
|
cellular phenotype
|
J:155408
|
Mapk12tm1Lex/Mapk12tm1Lex Tg(Myog-cre)1Eno/0
(involves: 129S/SvEvBrd)
|
decreased mitochondrial fission
|
J:155408
|
Mapk14tm1.1Dvb/Mapk14+
(B6(FVB)-Mapk14tm1.1Dvb)
|
decreased pancreatic beta cell proliferation
|
J:151980
|
increased pancreatic beta cell proliferation
|
J:151980
|
Mapk14tm1.1Dvb/Mapk14+ Ppm1dtm1Lad/Ppm1dtm1Lad
(involves: 129S7/SvEvBrd * C57BL/6)
|
cellular phenotype
|
J:151980
|
Mapk14tm1.1Lex/Mapk14tm1.1Lex
(involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J)
|
abnormal myoblast differentiation
|
J:119724
|
abnormal myoblast fusion
|
J:119724
|
increased myoblast proliferation
|
J:119724
|
Mapk14tm1.2Otsu/Mapk14tm1.2Otsu Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6J)
|
increased cardiomyocyte apoptosis
|
J:95116
|
Mapk14tm1Jda/Mapk14tm1Jda
(B6.Cg-Mapk14tm1Jda)
|
decreased T cell proliferation
|
J:146088
|
Mapk14tm1Lex/Mapk14tm1Lex Myl7tm1(cre)Krc/Myl7+
(involves: 129S1/Sv * 129S5/SvEvBrd * 129X1/SvJ * C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:98514
|
Mapk14tm1Lex/Mapk14tm1Lex Tg(Myog-cre)1Eno/0
(involves: 129S5/SvEvBrd)
|
cellular phenotype
|
J:155408
|
Mapk14tm1Mms/Mapk14tm1Mms
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:73417
|
Mapk14tm1Nbr/Mapk14tm1Nbr
(either: (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1))
|
increased embryonic tissue cell apoptosis
|
J:63877
|
Mapk14tm2Nbr/Mapk14tm2Nbr Polr2atm1(cre/ERT2)Bbd/Polr2a+
(involves: 129 * C57BL/6 * CD-1 * SJL)
|
abnormal cell cycle
|
J:122397
|
increased cell proliferation
|
J:122397
|
Mapkap1tm1Bisu/Mapkap1tm1Bisu
(B6.129S7-Mapkap1tm1Bisu)
|
increased cellular sensitivity to hydrogen peroxide
|
J:125618
|
increased fibroblast apoptosis
|
J:125618
|
Mapkapk2tm1Mgl/Mapkapk2tm1Mgl
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal macrophage derived foam cell morphology
|
J:142788
|
decreased cardiomyocyte apoptosis
|
J:101888
|
Mapkapk2tm1Mgl/Mapkapk2tm1Mgl
(involves: 129S * C57BL/6)
|
impaired macrophage phagocytosis
|
J:76161
|
Mapkapk2tm1Mgl/Mapkapk2tm1Mgl Tnftm2Gkl/Tnf+
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6J)
|
decreased apoptosis
|
J:108572
|
Mapkapk5tm1Pqs/Mapkapk5+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
delayed cellular replicative senescence
|
J:117893
|
Mapkapk5tm1Pqs/Mapkapk5tm1Pqs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
delayed cellular replicative senescence
|
J:117893
|
Mapttm1(Ewsr1/Etv4)Arbr/Mapt+ Mnx1tm4(cre)Tmj/Mnx1+
(involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6)
|
abnormal axon extension
|
J:100886
|
Mapttm1(MAPT)Vln/Mapttm1(MAPT)Vln
(involves: FVB/N)
|
abnormal axon extension
|
J:129032
|
increased cell proliferation
|
J:129032
|
Mapttm1Hnd/Mapt+ Zbtb20Tg(PDGFB-APPSwInd)20Lms/0
(involves: 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal neuron differentiation
|
J:121330
|
Mapttm1Hnd/Mapttm1Hnd
(involves: 129X1/SvJ * C57BL/6)
|
abnormal axon extension
|
J:78649
|
Mapttm1Hnd/Mapttm1Hnd Zbtb20Tg(PDGFB-APPSwInd)20Lms/0
(involves: 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal neuron differentiation
|
J:121330
|
Mapttm2.1(RHOA*)Klt/Mapt+
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
decreased neuron apoptosis
|
J:159220
|
Marchf5tm1.1Ygi/Marchf5tm1.1Ygi Tg(Emx1-cre)#Ito/0
(involves: C57BL/6)
|
abnormal mitochondrial crista morphology
|
J:284572
|
abnormal mitochondrial matrix morphology
|
J:284572
|
abnormal mitochondrial morphology
|
J:284572
|
decreased mitochondrial size
|
J:284572
|
oxidative stress
|
J:284572
|
Marchf7Gt(ROSABetageo)1Summ/Marchf7+
(involves: BALB/c)
|
increased T cell proliferation
|
J:96167
|
Marchf7Gt(ROSABetageo)1Summ/Marchf7Gt(ROSABetageo)1Summ
(involves: BALB/c)
|
increased T cell proliferation
|
J:96167
|
Marcotm1Ktry/Marcotm1Ktry
(B6.129S6-Marcotm1Ktry)
|
impaired macrophage phagocytosis
|
J:115081
|
Marcotm1Spt/Marcotm1Spt
(C57BL/6-Marcotm1Spt)
|
abnormal dendritic cell chemotaxis
|
J:204315
|
Marf1m1Rpg/Marf1m1Rpg
(B6;C3Fe-Marf1m1Rpg/J)
|
abnormal female meiosis I arrest
|
J:181834
|
Mark2tm1Hpw/Mark2tm1Hpw
(involves: 129X1/SvJ * C57BL/6)
|
decreased B cell proliferation
|
J:68830
|
increased adipocyte glucose uptake
|
J:120128
|
increased B cell proliferation
|
J:68830
|
increased mesangial cell number
|
J:68830
|
Mark3tm1Hpw/Mark3tm1Hpw
(involves: 129X1/SvJ * C57BL/6)
|
abnormal adipocyte glucose uptake
|
J:163905
|
Marveld1tm1.1Liy/Marveld1tm1.1Liy Tg(GFAP-cre)25Mes/0
(involves: C57BL/6J * FVB/N)
|
abnormal cerebellar granule cell migration
|
J:279065
|
Marveld1tm1.1Liy/Marveld1tm1.1Liy Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal cerebellar granule cell migration
|
J:279065
|
Marveld1tm1.2Liy/Marveld1tm1.2Liy
(involves: C57BL/6J)
|
abnormal cerebellar granule cell migration
|
J:279065
|
abnormal neuronal migration
|
J:279065
|
increased neuron apoptosis
|
J:279065
|
Mast1em1Dak/Mast1+
(B6.Cg-Mast1em1Dak)
|
increased neuron apoptosis
|
J:268904
|
Mast1em1Dak/Mast1em1Dak
(B6.Cg-Mast1em1Dak)
|
increased neuron apoptosis
|
J:268904
|
Mast4em1Sjkm/Mast4em1Sjkm
(C57BL/6J-Mast4em1Sjkm)
|
abnormal spermatogonia proliferation
|
J:340701
|
increased testis apoptosis
|
J:340701
|
oligozoospermia
|
J:340701
|
Mastltm1.1Mama/Mastltm1.1Mama
(Not Specified)
|
abnormal mitosis
|
J:201971
|
abnormal mitotic spindle morphology
|
J:201971
|
decreased fibroblast proliferation
|
J:201971
|
Mastltm1.1Mama/Mastltm1.1Mama Polr2atm1(cre/ERT2)Bbd/Polr2a+
(Not Specified)
|
abnormal mitosis
|
J:201971
|
Matcap1em1Nki/Matcap1em1Nki Svbpem1Mjom/Svbpem1Mjom
(involves: C57BL/6)
|
decreased neuronal precursor proliferation
|
J:325393
|
Matn1tm1Ref/Matn1tm1Ref Matn2tm1Asz/Matn2tm1Asz Matn3tm1Asz/Matn3tm1Asz Matn4tm1.1Asz/Matn4tm1.1Asz
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased hematopoietic stem cell proliferation
|
J:237230
|
Matn3tm1Mbri/Matn3tm1Mbri
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased chondrocyte proliferation
|
J:125104
|
increased chondrocyte apoptosis
|
J:125104
|
Matn4tm1.1Asz/Matn4tm1.1Asz
(B6.129-Matn4tm1.1Asz)
|
increased hematopoietic stem cell proliferation
|
J:237230
|
Matr3Gt(RRR075)Byg/Matr3+
(either: (involves: 129 * 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * C57BL/6J * FVB/N))
|
patent ductus arteriosus
|
J:220876
|
Mau2tm1.1Hpt/Mau2tm1.1Hpt H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S2/SvPas * C57BL/6 * C57BL/6J * CBA/J * SJL)
|
decreased cranial neural crest cell proliferation
|
J:213338
|
Mavstm1Camb/Mavstm1Camb
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased B cell proliferation
|
J:180356
|
Maxtm1Rdp/Maxtm1Rdp
(either: B6.Cg-Maxtm1Rdp or CD1.Cg-Maxtm1Rdp)
|
absent inner cell mass proliferation
|
J:59430
|
Mbtm1Wlm/Mbtm1Wlm
(Not Specified)
|
cellular phenotype
|
J:72560
|
Mbtm1Wlm/Mbtm1Wlm
(either: (involves: 129/Sv) or (involves: C57BL/6))
|
cellular phenotype
|
J:74121
|
Mbd1tm1Fhg/Mbd1tm1Fhg
(129S4/SvJae-Mbd1tm1Fhg)
|
abnormal neuron differentiation
|
J:83613
|
aneuploidy
|
J:83613
|
chromosomal instability
|
J:83613
|
chromosome breakage
|
J:83613
|
Mbd2tm1Bh/Mbd2tm1Bh
(NOD.129P2(B6)-Mbd2tm1Bh)
|
increased T cell proliferation
|
J:323838
|
Mbd3tm2Bh/Mbd3tm2Bh Tg(Vil1-cre)20Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
abnormal small intestinal crypt cell proliferation
|
J:167984
|
Mbd4/Ift122tm1Abc/Mbd4/Ift122tm1Abc
(either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal cell cycle checkpoint function
|
J:86981
|
decreased sensitivity to induced cell death
|
J:86981
|
Mbd4/Ift122tm1Abc/Mbd4/Ift122tm1Abc
(B6.129-Mbd4/Ift122tm1Abc)
|
abnormal cilium morphology
|
J:143544
|
absent embryonic cilia
|
J:143544
|
Mbd4/Ift122tm1Abc/Mbd4+
(B6.129-Mbd4/Ift122tm1Abc)
|
decreased embryonic cilium length
|
J:143544
|
Mbd4/Ift122tm1Abc/Ift122+
(B6.129-Mbd4/Ift122tm1Abc)
|
decreased embryonic cilium length
|
J:143544
|
Mbd4/Ift122tm1Abc/Mbd4/Ift122tm1Abc
(either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal cell cycle checkpoint function
|
J:86981
|
decreased sensitivity to induced cell death
|
J:86981
|
Mbd4/Ift122tm1Abc/Mbd4/Ift122tm1Abc
(B6.129-Mbd4/Ift122tm1Abc)
|
abnormal cilium morphology
|
J:143544
|
absent embryonic cilia
|
J:143544
|
Mbd4tm1Bird/Mbd4tm1Bird
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:77896
|
Mbd4tm1Wed/Mbd4tm1Wed
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:80319
|
Mbd4tm1Wed/Mbd4tm1Wed
(B6.Cg-Mbd4tm1Wed/J)
|
abnormal DNA methylation
|
J:175891
|
Mbd4tm2Abc/Mbd4tm2Abc
(involves: 129/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:86981
|
decreased sensitivity to induced cell death
|
J:86981
|
Mbl1tm1Kata/Mbl1tm1Kata Mbl2tm1Kata/Mbl2tm1Kata
(involves: 129 * C57BL/6)
|
impaired macrophage phagocytosis
|
J:97686,
J:98124
|
Mbnl1tm1Sws/Mbnl1tm1Sws Mbnl2tm1.1Sws/Mbnl2+
(involves: 129S1/Sv * 129S1/SvImJ * C57BL)
|
cardiac interstitial fibrosis
|
J:218011
|
Mboat7tm1Arai/Mboat7tm1Arai
(B6.129P2-Mboat7tm1Arai)
|
abnormal neuron differentiation
|
J:200247
|
abnormal neuronal migration
|
J:200247
|
increased neuron apoptosis
|
J:200247
|
Mboat7tm1Lex/Mboat7tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
cellular phenotype
|
J:185566
|
Mbpshi/Mbpshi
(involves: BALB/c * C3HeB/Fe * SWV)
|
increased T cell proliferation
|
J:48412
|
Mbpshi/Mbpshi Tg(Thy1-YFP)HJrs/0
(involves: C3HeB/Fe * C57BL/6 * CBA * SWV)
|
increased susceptibility to neuronal excitotoxicity
|
J:158545
|
Mbtps1tm1Jdh/Mbtps1tm1Jdh Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
(involves: 129S6/SvEvTac * C57BL/6 * CD-1)
|
increased chondrocyte apoptosis
|
J:258274
|
Mbtps1wrt/Mbtps1wrt
(C57BL/6J-Mbtps1wrt)
|
abnormal cell physiology
|
J:123123
|
Mc1re/Mc1re
(C57BL/6J-Mc1re/J)
|
abnormal keratinocyte apoptosis
|
J:112959
|
increased cellular sensitivity to ionizing radiation
|
J:112959
|
Mcattm1.1Ssmi/Mcattm1.1Ssmi Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA)
|
abnormal cellular respiration
|
J:192213
|
abnormal mitochondrial physiology
|
J:192213
|
Mcctm1.2Maija/Mcctm1.2Maija
(involves: BALB/cJ * C57BL/6)
|
abnormal DNA repair
|
J:294342
|
Mcemp1em1Jngj/Mcemp1em1Jngj
(C57BL/6-Mcemp1em1Jngj)
|
abnormal mast cell differentiation
|
J:335318
|
Mcidasem1Sroy/Mcidasem1Sroy
(C57BL/6-Mcidasem1Sroy)
|
abnormal brain ependyma motile cilium morphology
|
J:274880
|
abnormal cell differentiation
|
J:274880
|
abnormal motile cilium morphology
|
J:274880
|
abnormal oviduct epithelium motile cilium morphology
|
J:274880
|
Mcl1tm1Ywh/Mcl1tm1Ywh Tg(Cd4-cre)1Cwi/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2)
|
increased T cell apoptosis
|
J:137400
|
Mcl1tm1Ywh/Mcl1tm1Ywh Tg(Lck-cre)548Jxm/0
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * CBA)
|
increased T cell apoptosis
|
J:137400
|
Mcl1tm2Sjk/Mcl1tm3Sjk Tg(Lck-cre)1Cwi/0
(involves: 129X1/SvJ * C57BL/6 * DBA/2)
|
increased T cell apoptosis
|
J:86906
|
Mcm2Gt(AB0178)Wtsi/Mcm2+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm3Gt(RRR002)Byg/Mcm3+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm3Gt(RRR002)Byg/Mcm3+ Mcm4chaos3/Mcm4chaos3
(involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J)
|
chromosomal instability
|
J:165667
|
decreased fibroblast proliferation
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm3Gt(RRR002)Byg/Mcm3+ Mcm4Gt(RRE056)Byg/Mcm4+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm3Gt(RRR002)Byg/Mcm3+ Mcm4Gt(RRE056)Byg/Mcm4+ Mcm6Gt(YHD248)Byg/Mcm6+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm3Gt(RRR002)Byg/Mcm3+ Mcm4Gt(RRE056)Byg/Mcm4+ Mcm6Gt(YHD248)Byg/Mcm6+ Mcm7Gt(YTA285)Byg/Mcm7+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm3Gt(RRR002)Byg/Mcm3+ Mcm6Gt(YHD248)Byg/Mcm6+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm3Gt(RRR002)Byg/Mcm3+ Mcm6Gt(YHD248)Byg/Mcm6+ Mcm7Gt(YTA285)Byg/Mcm7+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm4chaos3/Mcm4chaos3
(involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J)
|
chromosomal instability
|
J:165667
|
decreased fibroblast proliferation
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm4Gt(RRE056)Byg/Mcm4+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2Gt(AB0178)Wtsi/Mcm2+ Mcm4Gt(RRE056)Byg/Mcm4+ Mcm6Gt(YHD248)Byg/Mcm6+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm2tm1(cre/ERT2)Scpr/Mcm2tm1(cre/ERT2)Scpr
(involves: 129S6/SvEvTac)
|
abnormal cell cycle
|
J:141493
|
abnormal cell nucleus morphology
|
J:141493
|
Mcm3Gt(RRR002)Byg/Mcm3+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm3Gt(RRR002)Byg/Mcm3+ Mcm4Gt(RRE056)Byg/Mcm4+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm3Gt(RRR002)Byg/Mcm3+ Mcm4Gt(RRE056)Byg/Mcm4+ Mcm6Gt(YHD248)Byg/Mcm6+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm3tm1.1Geno/Mcm3tm1.1Geno
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell cycle
|
J:227638
|
decreased DNA replication
|
J:227638
|
decreased hematopoietic stem cell proliferation
|
J:227638
|
increased apoptosis
|
J:227638
|
Mcm3aptm1Imku/Mcm3aptm1Imku Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased B cell proliferation
|
J:88276
|
Mcm4chaos3/Mcm4+
(involves: C57BL/6J)
|
abnormal cell nucleus morphology
|
J:117494
|
Mcm4chaos3/Mcm4chaos3
(involves: C57BL/6J)
|
abnormal cell nucleus morphology
|
J:117494
|
chromosomal instability
|
J:165667
|
Mcm4chaos3/Mcm4chaos3
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal cell cycle
|
J:117494
|
decreased cell proliferation
|
J:117494
|
Mcm4chaos3/Mcm4chaos3 Mcm7Gt(YTA285)Byg/Mcm7+
(involves: 129P2/OlaHsd * C3HeB/FeJ * C57BL/6J)
|
chromosomal instability
|
J:165667
|
Mcm4chaos3/Mcm4Gt(RRE056)Byg
(B6.Cg-Mcm4chaos3 Mcm4Gt(RRE056)Byg)
|
abnormal cell cycle
|
J:117494
|
decreased fibroblast proliferation
|
J:117494
|
induced chromosome breakage
|
J:117494
|
Mcm4Gt(RRE056)Byg/Mcm4+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm4Gt(RRE056)Byg/Mcm4Gt(RRE056)Byg
(involves: 129P2/OlaHsd)
|
absent inner cell mass proliferation
|
J:117494
|
Mcm4Sdla/Mcm4+
(involves: C57BL/6)
|
induced chromosome breakage
|
J:194117
|
spontaneous chromosome breakage
|
J:194117
|
Mcm6Gt(YHD248)Byg/Mcm6+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm7Gt(YTA285)Byg/Mcm7+
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
chromosomal instability
|
J:165667
|
Mcm8tm1.1Geno/Mcm8tm1.1Geno
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:187623
|
abnormal DNA replication
|
J:187623
|
abnormal double-strand DNA break repair
|
J:187623
|
abnormal male germ cell apoptosis
|
J:187623
|
abnormal oocyte morphology
|
J:187623
|
arrest of male meiosis
|
J:187623
|
azoospermia
|
J:187623
|
decreased fibroblast proliferation
|
J:187623
|
decreased oocyte number
|
J:187623
|
increased cellular sensitivity to gamma-irradiation
|
J:187623
|
polyploidy
|
J:187623
|
spontaneous chromosome breakage
|
J:187623
|
Mcm9Gt(AW0655)Wtsi/Mcm9Gt(AW0655)Wtsi
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
absent spermatogonia
|
J:177420
|
arrest of male meiosis
|
J:177420
|
decreased male germ cell number
|
J:177420
|
oligozoospermia
|
J:177420
|
Mcm9Gt(AW0655)Wtsi/Mcm9Gt(XG743)Byg
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
absent spermatogonia
|
J:177420
|
arrest of male meiosis
|
J:177420
|
decreased male germ cell number
|
J:177420
|
oligozoospermia
|
J:177420
|
Mcm9Gt(XG743)Byg/Mcm9Gt(XG743)Byg
(involves: 129P2/OlaHsd * C3HeB/FeJ)
|
abnormal cell cycle
|
J:177420
|
abnormal female germ cell morphology
|
J:177420
|
absent spermatogonia
|
J:177420
|
arrest of male meiosis
|
J:177420
|
decreased male germ cell number
|
J:177420
|
decreased oocyte number
|
J:177420
|
decreased primordial germ cell number
|
J:177420
|
early cellular replicative senescence
|
J:177420
|
oligozoospermia
|
J:177420
|
spontaneous chromosome breakage
|
J:177420
|
Mcm9tm1.1Geno/Mcm9tm1.1Geno
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:187623
|
abnormal DNA replication
|
J:187623
|
abnormal male germ cell apoptosis
|
J:187623
|
decreased fibroblast proliferation
|
J:187623
|
increased cellular sensitivity to gamma-irradiation
|
J:187623
|
oligozoospermia
|
J:187623
|
polyploidy
|
J:187623
|
spontaneous chromosome breakage
|
J:187623
|
Mcm10tm1Hlee/Mcm10tm1Hlee
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cell proliferation
|
J:177618
|
increased embryonic tissue cell apoptosis
|
J:177618
|
Mcmdc2tm3b(EUCOMM)Hmgu/Mcmdc2tm3b(EUCOMM)Hmgu
(involves: BALB/c * C57BL/6 * C57BL/6N * CD-1)
|
abnormal double-strand DNA break repair
|
J:236226
|
abnormal meiosis
|
J:236226
|
abnormal synaptonemal complex
|
J:236226
|
absent oocytes
|
J:236226
|
arrest of male meiosis
|
J:236226
|
azoospermia
|
J:236226
|
Mcmdc2tm3b(EUCOMM)Hmgu/Mcmdc2tm3b(EUCOMM)Hmgu Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * BALB/c * C57BL/6 * C57BL/6N * CD-1)
|
abnormal double-strand DNA break repair
|
J:236226
|
abnormal synaptonemal complex
|
J:236226
|
Mcoln2tm1e.1(KOMP)Wtsi/Mcoln2tm1e.1(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
impaired macrophage chemotaxis
|
J:239875
|
impaired neutrophil chemotaxis
|
J:239875
|
Mcph1Gt(RRO608)Byg/Mcph1Gt(RRO608)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal chromosome morphology
|
J:157993
|
abnormal mitosis
|
J:157993
|
Mcph1tm1.1Zqw/Mcph1tm1.1Zqw
(Not Specified)
|
abnormal cell cycle
|
J:180706
|
abnormal chromosome morphology
|
J:180706
|
abnormal mitosis
|
J:180706
|
abnormal mitotic spindle morphology
|
J:180706
|
abnormal neuron differentiation
|
J:180706
|
abnormal neuronal precursor proliferation
|
J:180706
|
increased neuron apoptosis
|
J:180706
|
Mcph1tm1.2Kali/Mcph1tm1.2Kali
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal male meiosis
|
J:156371
|
arrest of male meiosis
|
J:156371
|
decreased male germ cell number
|
J:156371
|
decreased spermatid number
|
J:156371
|
increased cellular sensitivity to gamma-irradiation
|
J:156371
|
increased male germ cell apoptosis
|
J:156371
|
induced chromosome breakage
|
J:156371
|
Mcph1tm1a(EUCOMM)Wtsi/Mcph1tm1a(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
chromosomal instability
|
J:213427
|
Mcpt1tm1Hrpm/Mcpt1tm1Hrpm
(involves: 129P2/OlaHsd * MF1)
|
decreased apoptosis
|
J:93616
|
Mcrip1tm1(KOMP)Vlcg/Mcrip1tm1(KOMP)Vlcg
(C57BL/6-Mcrip1tm1(KOMP)Vlcg)
|
abnormal epigenetic regulation of gene expression
|
J:278092
|
Mcrs1tm1.1(KOMP)Vlcg/Mcrs1tm1.1(KOMP)Vlcg
(B6N(Cg)-Mcrs1tm1.1(KOMP)Vlcg/J)
|
decreased inner cell mass proliferation
|
J:285737
|
McuGt(IST11669F8)Tigm/McuGt(IST11669F8)Tigm
(involves: C57BL/6 * C57BL/6N * CD-1)
|
abnormal mitochondrial physiology
|
J:208297
|
cellular phenotype
|
J:208297
|
Mcutm1.1Jmol/Mcutm1.1Jmol A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * FVB/N)
|
decreased cardiomyocyte apoptosis
|
J:224853
|
Mcutm1.1Jmol/Mcutm1.1Jmol Speer6-ps1Tg(Alb-cre)21Mgn/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA)
|
cellular phenotype
|
J:298361
|
Mcutm1.1Jmol/Mcutm1.1Jmol Tg(Cdh5-cre)7Mlia/0
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N)
|
abnormal mitochondrial physiology
|
J:235756
|
decreased lung endothelial cell migration
|
J:235756
|
decreased lung endothelial cell proliferation
|
J:235756
|
Mcutm1c(EUCOMM)Hmgu/Mcutm1c(EUCOMM)Hmgu Tg(Gabra6-cre)B1Lfr/0
(involves: C57BL/6N * DBA/2)
|
cellular phenotype
|
J:281635
|
Mcutm1c(EUCOMM)Hmgu/Mcutm1c(EUCOMM)Hmgu Tg(Pcp2-cre)2Mpin/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)
|
abnormal mitochondrial physiology
|
J:281635
|
Mcur1tm1c(KOMP)Wtsi/Mcur1tm1c(KOMP)Wtsi A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129S4/SvJaeSor * C57BL/6N * FVB/N)
|
abnormal mitochondrial physiology
|
J:235756
|
Mcur1tm1c(KOMP)Wtsi/Mcur1tm1c(KOMP)Wtsi Tg(Cdh5-cre)7Mlia/0
(involves: 129S4/SvJaeSor * C57BL/6N * FVB/N)
|
abnormal mitochondrial physiology
|
J:235756
|
decreased lung endothelial cell migration
|
J:235756
|
decreased lung endothelial cell proliferation
|
J:235756
|
Mdc1Gt(OST441263)Lex/Mdc1Gt(OST441263)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:137341
|
decreased cell proliferation
|
J:137341
|
increased cellular sensitivity to ionizing radiation
|
J:137341
|
oligozoospermia
|
J:137341
|
spontaneous chromosome breakage
|
J:137341
|
Mdga1tm1.1Tymo/Mdga1tm1.1Tymo
(B6.Cg-Mdga1tm1.1Tymo)
|
abnormal neuronal migration
|
J:166980
|
Mdga2Adp/Mdga2+
(involves: C57BL/6J * DBA/2)
|
abnormal DNA methylation
|
J:181260
|
Mdktm1Tmu/Mdktm1Tmu
(B6.129S2-Mdktm1Tmu)
|
abnormal macrophage chemotaxis
|
J:102069
|
impaired neutrophil chemotaxis
|
J:102069
|
mdlk1MOLF/Ei/?
(involves: C57BL/6J * MOLF/Ei)
|
abnormal imprinting
|
J:97841
|
Mdm2tm1.1Ypz/Mdm2tm1.1Ypz
(B6.129-Mdm2tm1.1Ypz)
|
increased cell proliferation
|
J:164200
|
Mdm2tm1Bay/Mdm2tm1Mep
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:81065
|
decreased cell proliferation
|
J:81065
|
increased cellular sensitivity to ionizing radiation
|
J:81065
|
Mdm2tm1Glo/Mdm2+
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:123661
|
Mdm2tm1Glo/Mdm2+ Mdm4Gt(VICTR20)7Lex/Mdm4+ Trp53tm1Wahl/Trp53tm1Wahl
(involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle
|
J:108183
|
Mdm2tm1Glo/Mdm2+ Mdm4Gt(VICTR20)7Lex/Mdm4+ Trp53tm3Wahl/Trp53tm3Wahl
(involves: 129)
|
abnormal cell cycle
|
J:108183
|
Mdm2tm1Glo/Mdm2+ Mdm4tm1Glo/Mdm4+
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:123661
|
increased embryonic tissue cell apoptosis
|
J:123661
|
Mdm2tm1Glo/Mdm2+ Trp53tm1.1Tldo/Trp53+
(involves: 129S2/SvPas * 129S7/SvEvBrd * BALB/c * C57BL/6)
|
decreased telomere length
|
J:199308
|
Mdm2tm1Glo/Mdm2+ Trp53tm1Wahl/Trp53tm1Wahl
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle
|
J:108183
|
Mdm2tm1Glo/Mdm2+ Trp53tm3Wahl/Trp53tm3Wahl
(involves: 129S4/SvJae * 129S7/SvEvBrd)
|
abnormal cell cycle
|
J:108183
|
Mdm2tm1Glo/Mdm2tm2.1Glo Tg(Myh6-cre)2182Mds/0
(involves: 129S7/SvEvBrd * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:104114
|
Mdm2tm2.1Snj/Mdm2tm2.1Snj
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:189297
|
decreased apoptosis
|
J:189297
|
decreased thymocyte apoptosis
|
J:189297
|
Mdm2tm3.1Glo/Mdm2tm3.1Glo
(B6.129S6-Mdm2tm3.1Glo)
|
decreased cellular sensitivity to ionizing radiation
|
J:164201
|
increased fibroblast proliferation
|
J:164201
|
Mdm2tm3.1Glo/Mdm2tm3.1Glo Trp53tm3.1Glo/Trp53+
(B6.129S-Mdm2tm3.1Glo Trp53tm3.1Glo)
|
decreased cellular sensitivity to ionizing radiation
|
J:164201
|
Mdm2tm3.1Snj/Mdm2tm3.1Snj
(involves: 129S4/SvJae * C57BL/6)
|
cellular phenotype
|
J:189297
|
Mdm2tm4.1Glo/Mdm2tm4.1Glo
(B6.129S6-Mdm2tm4.1Glo)
|
cellular phenotype
|
J:164201
|
Mdm4Gt(VICTR20)7Lex/Mdm4+ Trp53tm1Wahl/Trp53tm1Wahl
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell cycle
|
J:108183
|
Mdm4Gt(VICTR20)7Lex/Mdm4Gt(VICTR20)7Lex
(involves: 129S5/SvEvBrd)
|
abnormal cell cycle
|
J:77907
|
decreased cell proliferation
|
J:77907
|
Mdm4Gt(VICTR20)7Lex/Mdm4Gt(VICTR20)7Lex
(involves: 129S5/SvEvBrd * 129S6/SvEvTac * C57BL/6 * FVB/N)
|
decreased cell proliferation
|
J:166152
|
Mdm4Gt(VICTR20)7Lex/Mdm4Gt(VICTR20)7Lex Trp53tm1.1Xlu/Trp53tm1.1Xlu
(involves: 129S5/SvEvBrd * 129S6/SvEvTac * C57BL/6 * FVB/N)
|
cellular phenotype
|
J:166152
|
Mdm4Gt(VICTR20)7Lex/Mdm4Gt(VICTR20)7Lex Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * 129S5/SvEvBrd)
|
abnormal cell cycle checkpoint function
|
J:77907
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:77907
|
increased fibroblast proliferation
|
J:77907
|
Mdm4Gt(VICTR20)7Lex/Mdm4Gt(VICTR20)7Lex Trp53tm1Wahl/Trp53tm1Wahl
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell cycle
|
J:108183
|
decreased cell proliferation
|
J:108183
|
Mdm4Gt(VICTR20)7Lex/Mdm4Gt(VICTR20)7Lex Trp53tm3Wahl/Trp53tm3Wahl
(involves: 129S4/SvJae * 129S5/SvEvBrd)
|
abnormal cell cycle
|
J:108183
|
decreased fibroblast proliferation
|
J:108183
|
Mdm4tm1.1Wahl/Mdm4tm1.1Wahl
(involves: 129S/Sv * C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:150341
|
decreased thymocyte apoptosis
|
J:150341
|
Mdm4tm1Glo/Mdm4+
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell physiology
|
J:123661
|
Mdm4tm1Glo/Mdm4+ Trp53tm1.1Tldo/Trp53+
(involves: 129S2/SvPas * BALB/c * C57BL/6)
|
decreased telomere length
|
J:199308
|
Mdm4tm1Glo/Mdm4tm1Glo
(Not Specified)
|
decreased cell proliferation
|
J:71532
|
Mdm4tm1Zmy/Mdm4tm1Zmy
(involves: 129 * C57BL/6)
|
decreased cell proliferation
|
J:174359
|
increased embryonic tissue cell apoptosis
|
J:174359
|
Mdm4tm2Glo/Mdm4tm2.1Glo Tg(Myh6-cre)2182Mds/0
(involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:137114
|
MecomJbo/Mecom+
(C3N.C-MecomJbo)
|
abnormal neutrophil differentiation
|
J:113445
|
Mecp2tm1.1Bird/Mecp2+
(involves: 129P2/OlaHsd)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:108953
|
Mecp2tm1.1Mitoh/Y
(Not Specified)
|
increased placenta apoptosis
|
J:184364
|
Mecp2tm1.1Mitoh/Mecp2+
(Not Specified)
|
increased placenta apoptosis
|
J:184364
|
Mecp2tm1Hzo/Y
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:78009
|
Mecrtm1.1(fabI)Akast/Mecrtm1.1(fabI)Akast
(involves: C57BL/6 * C57BL/6JOlaHsd * C57BL/6N * SJL)
|
abnormal mitochondrial morphology
|
J:242847
|
abnormal mitochondrial physiology
|
J:242847
|
Med1tm1Rgr/Med1tm1Rgr
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * 129X1/SvJ))
|
abnormal cell cycle
|
J:61840
|
abnormal neuron apoptosis
|
J:61840
|
decreased fibroblast proliferation
|
J:61840
|
Med1tm2Jkr/Med1tm2Jkr A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129P2/OlaHsd * FVB/N)
|
cardiac interstitial fibrosis
|
J:243730
|
increased cardiomyocyte apoptosis
|
J:243730
|
Med1tm2Jkr/Med1tm2Jkr Tg(Myh6-cre)2182Mds/0
(involves: 129P2/OlaHsd * FVB/N)
|
cardiac interstitial fibrosis
|
J:243730
|
decreased myocardial fiber mitochondrial DNA content
|
J:243730
|
increased cardiomyocyte apoptosis
|
J:243730
|
Med1tm2Rgr/Med1tm2Rgr
(B6.129P2-Med1tm2Rgr)
|
decreased mammary gland epithelial cell proliferation
|
J:159303
|
Med12tm1Hsch/Y
(chimera involves: 129S6/SvEvTac * C57BL/6NCr)
|
abnormal neural crest cell migration
|
J:166040
|
Med19tm1c(EUCOMM)Wtsi/Med19tm1c(EUCOMM)Wtsi Tg(Adipoq-icre/ERT2)1Soff/0
(involves: C57BL/6J * C57BL/6N)
|
increased white adipose tissue apoptosis
|
J:298822
|
Med22tm1c(EUCOMM)Hmgu/Med22tm1c(EUCOMM)Hmgu Tg(Nphs1-cre)#Seq/0
(involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N)
|
increased podocyte apoptosis
|
J:300239
|
Med23tm1c(KOMP)Wtsi/Med23tm1c(KOMP)Wtsi H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
cellular phenotype
|
J:304767
|
Med23tm1Gwan/Med23tm1Gwan
(involves: 129 * C57BL/6)
|
abnormal cell differentiation
|
J:187746
|
Med24tm1Rgr/Med24tm1Rgr
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:77765
|
Med28tm1.2Vra/Med28tm1.2Vra
(involves: 129S4/SvJae * C57BL/6)
|
absent inner cell mass proliferation
|
J:243694
|
Med30m1Btlr/Med30m1Btlr
(involves: C57BL/6J)
|
abnormal mitochondrial morphology
|
J:180728
|
abnormal mitochondrial physiology
|
J:180728
|
Med31l11Jus15/Med31l11Jus15
(involves: 129S5/SvEvBrd * C57BL/6J)
|
decreased cell proliferation
|
J:161417
|
decreased fibroblast proliferation
|
J:161417
|
Mef2atm1.1Limm/Mef2atm1.1Limm Mef2ctm2Eno/Mef2ctm2Eno Mef2dtm3Eno/Mef2dtm3Eno Tg(GFAP-cre)25Mes/0
(involves: 129S/SvEv * C57BL/6 * FVB/N)
|
increased neuron apoptosis
|
J:207812
|
Mef2ctm1Eno/Mef2ctm1Jjs H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J * CBA/J)
|
abnormal melanocyte differentiation
|
J:173609
|
Mef2ctm1Jjs/Mef2ctm1Jjs Mir223tm1Fcam/Mir223tm1Fcam Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129 * C57BL/6)
|
abnormal neutrophil differentiation
|
J:140009
|
Mef2ctm1Jjs/Mef2ctm1Jjs Tg(Slc5a2-cre)1Tauc/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2)
|
increased kidney cell proliferation
|
J:158762
|
Mefvtm1Chae/Mefvtm1Chae
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6))
|
decreased macrophage apoptosis
|
J:82763
|
Meg3Gt(pGTi)216Gos/Meg3+
(involves: 129S2/SvPas * BALB/c * C57BL/6)
|
abnormal imprinting
|
J:108133,
J:125994
|
maternal imprinting
|
J:125994
|
Meg3Gt(pGTi)216Gos/Meg3+
(involves: 129S2/SvPas * C57BL/6)
|
abnormal imprinting
|
J:108133
|
Meg3Gt(pGTi)216Gos/Meg3Gt(pGTi)216Gos
(involves: 129S2/SvPas * BALB/c * C57BL/6)
|
abnormal imprinting
|
J:108133
|
Meg3Gt(pGTi)216Gos/Meg3Gt(pGTi)216Gos
(involves: 129S2/SvPas * C57BL/6)
|
abnormal imprinting
|
J:108133
|
Meg3tm1.1Jvs/Meg3+
(involves: 129P2/OlaHsd * FVB)
|
cellular phenotype
|
J:125994
|
Meg3tm1Itl/Meg3+
(B6.129S6-Meg3tm1Itl)
|
abnormal imprinting
|
J:166176
|
paternal imprinting
|
J:166176
|
Meg3tm1Jvs/Meg3+
(involves: 129P2/OlaHsd)
|
abnormal imprinting
|
J:125994
|
maternal imprinting
|
J:125994
|
Megf8Gt(G037A09)Wrst/Megf8m687Ddg
(involves: 129S6/SvEvTac * C3H/He * C57BL/6 * C57BL/6J)
|
abnormal axon fasciculation
|
J:206541
|
Megf8m687Ddg/Megf8m687Ddg
(involves: C3H/He * C57BL/6)
|
abnormal axon fasciculation
|
J:159834,
J:206541
|
Megf8tm1.1Ddg/Megf8tm1.1Ddg
(involves: 129S6/SvEvTac * BALB/cJ)
|
abnormal axon extension
|
J:206541
|
abnormal axon fasciculation
|
J:206541
|
Megf8tm1.2Ddg/Megf8tm1.2Ddg H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S6/SvEvTac * C57BL/6J * CBA/J)
|
abnormal axon fasciculation
|
J:206541
|
Megf10tm1(KOMP)Vlcg/Megf10+
(C57BL/6N-Megf10tm1(KOMP)Vlcg)
|
increased hindbrain apoptosis
|
J:231811
|
Megf10tm1(KOMP)Vlcg/Megf10tm1(KOMP)Vlcg
(C57BL/6N-Megf10tm1(KOMP)Vlcg)
|
increased hindbrain apoptosis
|
J:231811
|
Mei1m1Jcs/Mei1m1Jcs
(involves: 129S1/Sv * C57BL/6J)
|
abnormal female meiosis
|
J:60747
|
arrest of male meiosis
|
J:60747
|
azoospermia
|
J:60747
|
Mei1m1Jcs/Mei1m1Jcs
(involves: 129S1/Sv)
|
abnormal male meiosis
|
J:194067
|
mei2-7/mei2-7
(involves: 129S1/Sv * C57BL/6)
|
arrest of male meiosis
|
J:86161
|
Mei4tm1Bdm/Mei4tm1Bdm
(involves: 129S2/SvPas)
|
abnormal chromosomal synapsis
|
J:161203
|
abnormal meiosis
|
J:161203
|
abnormal spermatocyte morphology
|
J:276412
|
abnormal synaptonemal complex
|
J:161203
|
arrest of male meiosis
|
J:161203
|
azoospermia
|
J:161203
|
increased testis apoptosis
|
J:161203
|
mei7/mei7
(involves: C3HeB/FeJ * C57BL/6)
|
arrest of male meiosis
|
J:86161
|
mei11b/mei11b
(involves: C3HeB/FeJ * C57BL/6)
|
abnormal female meiosis
|
J:86161
|
Meig1tm1.1Zzha/Meig1tm1.1Zzha Tg(Hspa2-cre)1Eddy/0
(involves: C57BL/6 * C57BL/6J)
|
abnormal manchette assembly
|
J:194944
|
abnormal sperm axoneme morphology
|
J:194944
|
abnormal sperm head morphology
|
J:194944
|
abnormal sperm nucleus morphology
|
J:194944
|
abnormal spermatid morphology
|
J:194944
|
absent sperm flagellum
|
J:194944
|
globozoospermia
|
J:194944
|
immotile sperm
|
J:194944
|
oligozoospermia
|
J:194944
|
Meig1tm1.2Zzha/Meig1tm1.2Zzha
(Not Specified)
|
abnormal sperm axoneme morphology
|
J:153677
|
abnormal sperm head morphology
|
J:153677
|
absent sperm flagellum
|
J:153677
|
asthenozoospermia
|
J:153677
|
azoospermia
|
J:153677
|
Meig1tm1Shpi/Meig1tm1Shpi
(involves: 129S1/Sv * 129X1/SvJ * BALB/c)
|
abnormal sperm flagellum morphology
|
J:156715
|
abnormal sperm head morphology
|
J:156715
|
enlarged sperm head
|
J:156715
|
immotile sperm
|
J:156715
|
increased male germ cell apoptosis
|
J:156715
|
oligozoospermia
|
J:156715
|
teratozoospermia
|
J:156715
|
Meikintm1Yow/Meikintm1Yow
(involves: C57BL/6)
|
abnormal chromosomal synapsis
|
J:216866
|
abnormal female meiosis
|
J:216866
|
abnormal male meiosis
|
J:216866
|
abnormal spermatid morphology
|
J:216866
|
arrest of male meiosis
|
J:216866
|
impaired polar body extrusion
|
J:216866
|
oligozoospermia
|
J:216866
|
Meikintm1Yow/Meikintm1Yow Mlh1tm1Lisk/Mlh1tm1Lisk
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal chromosomal synapsis
|
J:216866
|
Meiobtm1.1Ics/Meiobtm1.1Ics
(involves: C57BL/6NTac)
|
abnormal double-strand DNA break repair
|
J:203426
|
abnormal meiosis
|
J:203426
|
absent oocytes
|
J:203426
|
azoospermia
|
J:203426
|
decreased oocyte number
|
J:203426
|
increased male germ cell apoptosis
|
J:203426
|
increased ovary apoptosis
|
J:203426
|
Meiobtm1.1Jw/Meiobtm1.1Jw
(involves: 129S4/SvJae * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:292036
|
Meioctm1a(KOMP)Wtsi/Meioctm1a(KOMP)Wtsi
(involves: C57BL/6 * C57BL/6N * NMRI)
|
abnormal double-strand DNA break repair
|
J:231231
|
abnormal female meiosis I arrest
|
J:231231
|
abnormal synaptonemal complex
|
J:231231
|
absent oocytes
|
J:231231
|
arrest of male meiosis
|
J:231231
|
azoospermia
|
J:231231
|
decreased male germ cell number
|
J:231231
|
decreased oocyte number
|
J:231231
|
increased male germ cell apoptosis
|
J:231231
|
Meioctm1a(KOMP)Wtsi/Meioctm1a(KOMP)Wtsi Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * C57BL/6N)
|
absent oocytes
|
J:231231
|
arrest of male meiosis
|
J:231231
|
azoospermia
|
J:231231
|
Meioctm1c(KOMP)Wtsi/Meioctm1c(KOMP)Wtsi Tg(Ddx4-cre)1Dcas/0
(involves: 129S4/SvJaeSor * C57BL/6N * FVB)
|
azoospermia
|
J:231231
|
Meiosinem1Keish/Meiosinem1Keish
(involves: C57BL/6 * C57BL/6N)
|
abnormal female meiosis
|
J:290712
|
abnormal female meiosis I arrest
|
J:290712
|
abnormal male meiosis
|
J:290712
|
abnormal meiotic configurations
|
J:290712
|
abnormal synaptonemal complex
|
J:290712
|
absent chiasmata formation
|
J:290712
|
arrest of male meiosis
|
J:290712
|
azoospermia
|
J:290712
|
increased male germ cell apoptosis
|
J:290712
|
Meis1tm2Ngc/Meis1tm2Ngc Tg(Tal1-cre/ERT)42-056Jrg/0
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J)
|
oxidative stress
|
J:192126
|
Meis2tm1.2Zkoz/Meis2tm1.2Zkoz
(involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J)
|
increased embryonic tissue cell apoptosis
|
J:229604
|
increased hepatocyte apoptosis
|
J:229604
|
Memo1tm1.1Neh/Memo1tm1.1Neh Tg(CAG-cre/Esr1*)1Lbe/0
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
azoospermia
|
J:206626
|
Men1tm1.1Zqw/Men1tm1.1Zqw
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell differentiation
|
J:83882
|
Men1tm1.2Zqw/Men1tm1.2Zqw Pgrtm2(cre)Lyd/Pgr+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal DNA methylation
|
J:322043
|
Meox2tm1(cre)Sor/Meox2+ Rasgrf1tm4.1Pds/Rasgrf1+
(involves: 129S4/SvJaeSor * C57BL/6)
|
cellular phenotype
|
J:117666
|
Meox2tm1(cre)Sor/Meox2+ Snai1tm1Grid/Snai1tm2Grid
(involves: 129S1/Sv * 129S4/SvJaeSor)
|
increased allantois apoptosis
|
J:111702
|
Meox2tm1(cre)Sor/Meox2+ Xrcc1tm1Pmc/Xrcc1tm1Pmc
(involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:152528
|
Mertknmf12/Mertknmf12
(involves: C57BL/6J)
|
increased retina apoptosis
|
J:175587
|
Mertktm1Gkm/Mertktm1Gkm
(NOD.129P2-Mertktm1Gkm)
|
increased T cell apoptosis
|
J:147153
|
Mertktm1Gkm/Mertktm1Gkm Tg(TcraBDC2.5,TcrbBDC2.5)1Doi/0
(NOD.Cg-Mertktm1Gkm Tg(TcraBDC2.5,TcrbBDC2.5)1Doi)
|
increased T cell apoptosis
|
J:147153
|
Mertktm1Grl/Mertktm1Grl Tyro3tm1Grl/Tyro3tm1Grl
(involves: 129S1/Sv * 129X1/SvJ)
|
oligozoospermia
|
J:54681
|
Mesp1tm2(cre)Ysa/Mesp1+ Tbx1tm1Bld/Tbx1tm3Bld
(involves: 129S7/SvEvBrd * C57BL/6 * CBA)
|
abnormal cardiac neural crest cell migration
|
J:112457
|
abnormal cranial neural crest cell migration
|
J:112457
|
Mesp1tm2(cre)Ysa/Mesp1+ Tbx1tm1Bld/Tbx1tm5Bld
(involves: 129S7/SvEvBrd * C57BL/6 * CBA)
|
abnormal neural crest cell migration
|
J:112457
|
Mesp2tm1Ysa/Mesp2tm1Ysa
(either: (involves: C57BL/6 * CBA) or (involves: C57BL/6 * CBA * ICR))
|
abnormal axon extension
|
J:42014
|
Mesttm1Masu/Mest+
(involves: 129S1/Sv * 129X1/SvJ)
|
maternal imprinting
|
J:79223,
J:50170
|
Mesttm1Masu/Mest+
(involves: C57BL/6)
|
maternal imprinting
|
J:50170
|
Mesttm1Masu/Mest+
(involves: BALB/c)
|
maternal imprinting
|
J:50170
|
Mesttm1Masu/Mest+
(involves: C57BL/6 * CBA/Ca)
|
maternal imprinting
|
J:50170
|
Mettm1Cbm/Mettm1Cbm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal muscle precursor cell migration
|
J:28570
|
Mettm1Cbm/Mettm1Cbm
(involves: ICR)
|
abnormal muscle precursor cell migration
|
J:80685
|
Mettm1Cpo/Mettm1Cpo
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal axon extension
|
J:174591
|
Mettm1Gvw/Met+
(involves: 129 * C57BL/6J)
|
chromosome breakage
|
J:94722
|
Mettm1Kln/Mettm1Kln
(involves: 129/Sv * C57BL/6 * CD-1)
|
abnormal myoblast migration
|
J:94030
|
Mettm1Sst/Mettm1Sst Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased hepatocyte apoptosis
|
J:89236
|
Mettm1Sst/Mettm1Sst Tg(Pdx1-cre)89.1Dam/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased pancreatic beta cell proliferation
|
J:196854
|
Mettm1Sst/Mettm1Sst Trp53tm1Brn/Trp53tm1Brn
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:175978
|
Mettm1Sst/Mettm1Sst Trp53tm1Brn/Trp53tm2Tyj
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
cellular phenotype
|
J:175978
|
Mettm1Sst/Mettm1Sst Trp53tm1Brn/Trp53tm3Tyj
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
cellular phenotype
|
J:175978
|
Mettm2Cpo/Mettm4.1Cpo
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuron differentiation
|
J:81793
|
Mettm2Gvw/Met+
(involves: 129 * C57BL/6J)
|
chromosome breakage
|
J:94722
|
Mettm2Kln/Mettm2Kln
(involves: 129/Sv * C57BL/6 * CD-1)
|
abnormal myoblast migration
|
J:94030
|
Mettm3Gvw/Mettm3Gvw
(involves: 129 * C57BL/6J)
|
chromosome breakage
|
J:94722
|
Mettm4Gvw/Met+
(involves: 129 * C57BL/6J)
|
chromosome breakage
|
J:94722
|
Metap2tm1.2Ccr/Metap2tm1.2Ccr
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N)
|
decreased cell proliferation
|
J:111701
|
Mettl1em1Bcgen/Mettl1em1Bcgen Tg(Prrx1-cre)1Cjt/0
(involves: C57BL/6J * SJL/J)
|
abnormal cell physiology
|
J:355649
|
abnormal cellular respiration
|
J:355649
|
abnormal mitochondrial physiology
|
J:355649
|
decreased cellular glucose uptake
|
J:355649
|
decreased chondrocyte proliferation
|
J:355649
|
increased cellular ATP level
|
J:355649
|
Mettl2em1Nju/Mettl2em1Nju
(Not Specified)
|
abnormal cell physiology
|
J:241777
|
Mettl3em1Chhe/Mettl3em1Chhe Mettl14em1Chhe/Mettl14em1Chhe Stra8em1(GFP/cre)Smoc/Stra8+
(involves: C57BL/6J)
|
abnormal elongated spermatid morphology
|
J:250428
|
abnormal epigenetic regulation of gene expression
|
J:250428
|
abnormal sperm head morphology
|
J:250428
|
abnormal translation
|
J:250428
|
asthenozoospermia
|
J:250428
|
decreased elongated spermatid number
|
J:250428
|
decreased sperm progressive motility
|
J:250428
|
oligozoospermia
|
J:250428
|
teratozoospermia
|
J:250428
|
Mettl3em1Chhe/Mettl3em1Chhe Mettl14em1Chhe/Mettl14em1Chhe Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6J * FVB)
|
absent spermatogonia
|
J:250428
|
decreased male germ cell number
|
J:250428
|
Mettl3em1Chhe/Mettl3em1Chhe Stra8em1(GFP/cre)Smoc/Stra8+
(involves: C57BL/6J)
|
abnormal epigenetic regulation of gene expression
|
J:250428
|
Mettl3em1Chhe/Mettl3em1Chhe Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6J * FVB)
|
abnormal epigenetic regulation of gene expression
|
J:250428
|
abnormal male germ cell morphology
|
J:250428
|
abnormal spermatogonia proliferation
|
J:250428
|
abnormal translation
|
J:250428
|
absent spermatogonia
|
J:250428
|
decreased male germ cell number
|
J:250428
|
decreased spermatogonia number
|
J:250428
|
Mettl3tm1.1Jhha/Mettl3tm1.1Jhha Tg(Stra8-icre)1Reb/0
(involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * FVB/NJ)
|
oligozoospermia
|
J:299108
|
Mettl3tm1.1Jhha/Mettl3tm1.1Jhha Tg(Zp3-cre)93Knw/0
(involves: 129S4/SvJaeSor * BALB/c * C57BL/6 * C57BL/6J)
|
abnormal female meiosis
|
J:299108
|
abnormal oocyte morphology
|
J:299108
|
decreased oocyte number
|
J:299108
|
Mettl5em1Schne/Mettl5em1Schne
(involves: C57BL/6NCrl)
|
abnormal spermatogonia morphology
|
J:289086
|
Mettl6em1Nju/Mettl6em1Nju
(Not Specified)
|
abnormal cell physiology
|
J:241777
|
Mettl8em1Nju/Mettl8em1Nju
(Not Specified)
|
abnormal cell physiology
|
J:241777
|
Mettl9em1Yshk/Mettl9em1Yshk
(C57BL/6J-Mettl9em1Yshk)
|
abnormal DNA methylation
|
J:302655
|
Mettl14em1Chhe/Mettl14em1Chhe Stra8em1(GFP/cre)Smoc/Stra8+
(involves: C57BL/6J)
|
abnormal epigenetic regulation of gene expression
|
J:250428
|
Mettl14em1Chhe/Mettl14em1Chhe Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6J * FVB)
|
abnormal epigenetic regulation of gene expression
|
J:250428
|
abnormal translation
|
J:250428
|
absent spermatogonia
|
J:250428
|
decreased male germ cell number
|
J:250428
|
Mettl14tm1.1Czhao/Mettl14tm1.1Czhao Tg(Nes-cre)1Kln/0
(involves: 129S6/SvEvTac * C57BL/6NCrl * SJL)
|
decreased radial glial cell number
|
J:258043
|
Mettl14tm1.2Czhao/Mettl14tm1.2Czhao
(involves: 129S6/SvEvTac * C57BL/6NCrl * FVB/N * SJL)
|
abnormal DNA methylation
|
J:258043
|
premature neuronal precursor differentiation
|
J:258043
|
Mettl15em1Pvs/Mettl15em1Pvs
(involves: C57BL/6 * CBA)
|
early cellular replicative senescence
|
J:325995
|
increased mitochondrial DNA content
|
J:325995
|
Mettl21ctm1.1Krug/Mettl21ctm1.1Krug
(involves: 129 * C57BL/6)
|
abnormal autophagy
|
J:270838
|
Mettl23em1Ogu/Mettl23em1Ogu
(involves: C57BL/6 * DBA/2)
|
abnormal DNA methylation
|
J:254851
|
Mex3atm1.1(KOMP)Vlcg/Mex3atm1.1(KOMP)Vlcg
(involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6NTac)
|
abnormal gastrointestinal brush cell morphology
|
J:287423
|
abnormal small intestinal crypt cell proliferation
|
J:287423
|
Mex3btm1.2Mbld/Mex3btm1.2Mbld
(involves: C57BL/6 * CBA)
|
impaired macrophage phagocytosis
|
J:213588
|
oligozoospermia
|
J:213588
|
Mexistm1.1Pton/Mexistm1.1Pton
(involves: C57BL/6)
|
decreased cholesterol efflux
|
J:264834
|
increased macrophage derived foam cell number
|
J:264834
|
MffGt(AZ0438)Wtsi/MffGt(AZ0438)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased apoptosis
|
J:255071
|
MffGt(AZ0438)Wtsi/MffGt(AZ0438)Wtsi
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:301349
|
abnormal mitochondrial morphology
|
J:301349
|
abnormal sperm midpiece morphology
|
J:301349
|
abnormal sperm mitochondrial sheath morphology
|
J:301349
|
decreased mitochondrial number
|
J:301349
|
dilated mitochondrion
|
J:301349
|
increased mitochondrial size
|
J:301349
|
increased sperm mitochondrial size
|
J:301349
|
Mfge8Gt(KST227)Byg/Mfge8Gt(KST227)Byg
(B6.129P2-Mfge8Gt(KST227)Byg)
|
impaired macrophage phagocytosis
|
J:98314
|
Mfge8Gt(KST227)Byg/Mfge8Gt(KST227)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired macrophage phagocytosis
|
J:107106
|
Mfge8tm1Osa/Mfge8tm1Osa
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
impaired macrophage phagocytosis
|
J:90633
|
Mfge8tm1Osa/Mfge8tm1Osa Timd4tm1Osa/Timd4tm1Osa
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
impaired macrophage phagocytosis
|
J:187181
|
Mfge8tm1Shur/Mfge8tm1Shur
(B6.129-Mfge8tm1Shur)
|
abnormal cell adhesion
|
J:145962
|
Mfn1tm1Dcc/Mfn1tm1Dcc
(involves: 129S/SvEv)
|
abnormal mitochondrial morphology
|
J:81438
|
abnormal mitochondrial physiology
|
J:81438
|
Mfn1tm1Dcc/Mfn1tm2Dcc
(involves: 129 * 129S4/SvJaeSor * Black Swiss)
|
abnormal mitochondrial morphology
|
J:132329
|
Mfn1tm1Dcc/Mfn1tm2Dcc Mfn2tm1Dcc/Mfn2tm3Dcc Tg(Pcp2-cre)2Mpin/0
(involves: 129 * 129S4/SvJaeSor * Black Swiss)
|
abnormal respiratory electron transport chain
|
J:132329
|
Mfn1tm2Dcc/Mfn1tm2Dcc Mfn2tm3Dcc/Mfn2tm3Dcc Tg(Stra8-icre)1Reb/0
(involves: 129 * C57BL/6J * FVB/NJ)
|
abnormal mitochondrial morphology
|
J:305430
|
abnormal spermatocyte morphology
|
J:305430
|
arrest of male meiosis
|
J:305430
|
decreased male germ cell number
|
J:305430
|
decreased round spermatid number
|
J:305430
|
Mfn1tm2Dcc/Mfn1tm2Dcc Tg(Stra8-icre)1Reb/0
(involves: 129 * C57BL/6J * FVB/NJ)
|
abnormal male germ cell morphology
|
J:305430
|
abnormal male germ cell physiology
|
J:305430
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:305430
|
abnormal mitochondrial morphology
|
J:305430
|
cellular phenotype
|
J:305430
|
increased mitochondrial DNA content
|
J:305430
|
increased mitochondrial fission
|
J:305430
|
oligozoospermia
|
J:305430
|
Mfn2em1Cya/Mfn2em1Cya Tg(Stra8-icre)1Reb/0
(involves: C57BL/6J * FVB/NJ)
|
abnormal male meiosis
|
J:324164
|
abnormal sperm mitochondrial sheath morphology
|
J:324164
|
abnormal sperm nucleus morphology
|
J:324164
|
kinked sperm flagellum
|
J:324164
|
Mfn2tm1.1Arte/Mfn2tm1.1Arte Slc6a3tm1(cre)Lrsn/Slc6a3+
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal respiratory electron transport chain
|
J:188337
|
Mfn2tm1.1Balo/Mfn2tm1.1Balo
(Not Specified)
|
abnormal mitochondrial physiology
|
J:159219
|
Mfn2tm1.1Mzhe/Mfn2tm1.1Mzhe
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:188865
|
Mfn2tm1.1Mzhe/Mfn2tm1.1Mzhe Myl2tm1(cre)Krc/Myl2+
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J)
|
abnormal autophagy
|
J:188865
|
abnormal cellular respiration
|
J:188865
|
abnormal mitochondrial morphology
|
J:188865
|
increased fetal cardiomyocyte apoptosis
|
J:188865
|
Mfn2tm1Dcc/Mfn2tm1Dcc
(involves: 129S/SvEv)
|
abnormal mitochondrial morphology
|
J:81438
|
abnormal mitochondrial physiology
|
J:81438
|
Mfn2tm1Dcc/Mfn2tm3Dcc
(involves: 129 * 129S4/SvJaeSor * Black Swiss)
|
abnormal mitochondrial morphology
|
J:132329
|
Mfn2tm1Dcc/Mfn2tm3Dcc Tg(Pcp2-cre)2Mpin/0
(involves: 129 * 129S4/SvJaeSor * Black Swiss)
|
abnormal Purkinje cell mitochondrial morphology
|
J:132329
|
abnormal respiratory electron transport chain
|
J:132329
|
Mfn2tm2Dcc/Mfn2tm2Dcc
(involves: 129S/SvEv * FVB/N)
|
abnormal mitochondrial morphology
|
J:119702
|
Mfn2tm2Dcc/Mfn2tm2Dcc
(involves: 129S/SvEv)
|
abnormal mitochondrial physiology
|
J:159219
|
Mfn2tm3Dcc/Mfn2tm3Dcc Tg(Stra8-icre)1Reb/0
(involves: 129 * C57BL/6J * FVB/NJ)
|
abnormal endoplasmic reticulum morphology
|
J:305430
|
abnormal male germ cell morphology
|
J:305430
|
abnormal male germ cell physiology
|
J:305430
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:305430
|
abnormal mitochondrial morphology
|
J:305430
|
abnormal sperm head morphology
|
J:305430
|
abnormal spermatid morphology
|
J:305430
|
abnormal spermatocyte morphology
|
J:305430
|
absent sperm head
|
J:305430
|
cellular phenotype
|
J:305430
|
coiled sperm flagellum
|
J:305430
|
decreased male germ cell number
|
J:305430
|
decreased round spermatid number
|
J:305430
|
increased male germ cell apoptosis
|
J:305430
|
increased mitochondrial DNA content
|
J:305430
|
increased mitochondrial fission
|
J:305430
|
increased testis apoptosis
|
J:305430
|
oligozoospermia
|
J:305430
|
teratozoospermia
|
J:305430
|
Mfngtm1.1Cfg/Mfngtm1.1Cfg
(involves: C57BL/6)
|
increased B cell proliferation
|
J:217719
|
Mfsd2atm1Dls/Mfsd2atm1Dls
(B6.Cg-Mfsd2atm1Dls)
|
increased fatty acid oxidation
|
J:194781
|
Mfsd2atm1Lex/Mfsd2atm1Lex
(B6;129S5-Mfsd2atm1Lex/Mmucd)
|
abnormal vesicle-mediated transport
|
J:210589
|
Mfsd6lem1Fzh/Mfsd6lem1Fzh
(C57BL/6-Mfsd6lem1Fzh)
|
abnormal acrosome morphology
|
J:359004
|
abnormal sperm head morphology
|
J:359004
|
asthenozoospermia
|
J:359004
|
decreased sperm progressive motility
|
J:359004
|
detached acrosome
|
J:359004
|
oligozoospermia
|
J:359004
|
teratozoospermia
|
J:359004
|
Mfsd8tm1a(EUCOMM)Hmgu/Mfsd8tm1a(EUCOMM)Hmgu
(involves: C57BL/6N)
|
abnormal lysosome morphology
|
J:211608
|
Mfsd14atm1Coll/Mfsd14atm1Coll
(involves: 129S/SvEv * 129S6/SvEvTac)
|
abnormal sperm head morphology
|
J:230570
|
absent acrosome
|
J:230570
|
absent sperm mitochondrial sheath
|
J:230570
|
globozoospermia
|
J:230570
|
oligozoospermia
|
J:230570
|
MgaGt(E153E01)Wrst/MgaGt(E153E01)Wrst
(involves: 129P2/OlaHsd * ICR)
|
increased embryonic tissue cell apoptosis
|
J:217679
|
increased inner cell mass apoptosis
|
J:217679
|
Mgat1tm2Jxm/Mgat1tm1Pst Tg(Zp3-cre)1Gwh/0
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal oogenesis
|
J:94224
|
abnormal zona pellucida morphology
|
J:94224
|
thin zona pellucida
|
J:94224
|
Mgat1tm2Jxm/Mgat1tm2Jxm Tg(Stra8-icre)1Reb/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/NJ)
|
azoospermia
|
J:260130
|
decreased elongated spermatid number
|
J:260130
|
multinucleated giant male germ cells
|
J:260130
|
Mgat1tm2Jxm/Mgat1tm2Jxm Tg(Zp3-cre)1Gwh/0
(Not Specified)
|
abnormal oogenesis
|
J:94224
|
abnormal zona pellucida morphology
|
J:94224
|
thin zona pellucida
|
J:94224
|
Mgat2tm1.1Jxm/Mgat2tm1.1Jxm
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
arrest of male meiosis
|
J:80661
|
azoospermia
|
J:80661
|
Mgat3tm1Pst/Mgat3tm1Pst
(involves: 129/Sv * C57BL/6 * CD-1 * SJL)
|
decreased hepatocyte proliferation
|
J:86643
|
Mgat4atm1.1Jxm/Mgat4atm1.1Jxm
(B6.Cg-Mgat4atm1.1Jxm)
|
decreased cellular glucose uptake
|
J:117542
|
Mgme1tm1.1Lrsn/Mgme1tm1.1Lrsn Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6NTac * FVB)
|
decreased mitochondrial DNA content
|
J:259702
|
Mgme1tm1.2Lrsn/Mgme1tm1.2Lrsn
(involves: C57BL/6NTac)
|
abnormal mitochondrial physiology
|
J:259702
|
decreased mitochondrial DNA content
|
J:259702
|
Mgptm1Kry/Mgptm1Kry
(involves: 129S7/SvEvBrd)
|
abnormal osteoblast physiology
|
J:203924
|
Mgst2Gt(OST22210)Lex/Mgst2Gt(OST22210)Lex
(involves: 129S5/SvEvBrd)
|
decreased endoplasmic reticulum stress
|
J:228296
|
decreased fibroblast apoptosis
|
J:228296
|
Mhstq1M. macedonius/Mhstq1M. macedonius
(involves: C57BL/6J * M. macedonius)
|
abnormal sperm head morphology
|
J:94029
|
absent sperm flagellum
|
J:94029
|
Mhstq2M. macedonius/Mhstq2M. macedonius
(involves: C57BL/6J * M. macedonius)
|
abnormal male meiosis
|
J:94029
|
abnormal sperm head morphology
|
J:94029
|
absent sperm head
|
J:94029
|
azoospermia
|
J:94029
|
Mia3tm1Lex/Mia3tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell morphology
|
J:172737
|
abnormal cell physiology
|
J:172737
|
Mib1tm1Art/Mib1tm1Art
(BTNTTFArt.129S-Mib1tm1Art)
|
premature neuronal precursor differentiation
|
J:102528
|
Mib1tm1Kong/Mib1tm1Kong
(either: B6.129P2-Mib1tm1Kong or (involves: 129P2/OlaHsd * FVB/N))
|
abnormal vascular regression
|
J:101173
|
premature neuronal precursor differentiation
|
J:101173
|
Mib1tm2Kong/Mib1tm2Kong Foxa2tm3.1(icre)Heli/Foxa2+
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal pancreatic beta cell differentiation
|
J:184814
|
Mib1tm2Kong/Mib1tm2Kong Tg(GFAP-cre)25Mes/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
delayed neuronal migration
|
J:130369
|
Mib1tm2Kong/Mib1tm2Kong Tg(Msx2-cre)5Rem/0
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal interdigital cell death
|
J:130369
|
Mib1tm2Kong/Mib1tm2Kong Tg(Tek-cre)12Flv/0
(involves: 129P2/OlaHsd * C3H * C57BL/6)
|
abnormal vascular regression
|
J:130369
|
Mical1tm1.2Past/Mical1tm1.2Past
(involves: 129)
|
abnormal cell morphology
|
J:240378
|
Micu1em#Fink/Micu1em#Fink
(C57BL/6N-Micu1em#Fink)
|
abnormal mitochondrial morphology
|
J:238984
|
abnormal mitochondrial physiology
|
J:238984
|
increased B cell apoptosis
|
J:238984
|
oxidative stress
|
J:238984
|
Micu1em#Fink/Micu1em#Fink Smdt1em1Fink/Smdt1+
(involves: C57BL/6J * C57BL/6N * CBA)
|
abnormal mitochondrial physiology
|
J:238984
|
Micu2Gt(OST409343)Lex/Micu2Gt(OST409343)Lex
(B6.129S5-Micu2Gt(OST409343)Lex)
|
abnormal mitochondrial physiology
|
J:249367
|
abnormal myocardial fiber mitochondrial morphology
|
J:249367
|
decreased mitochondrial size
|
J:249367
|
Mideasem1Shmc/Mideasem1Shmc
(C57BL/6J-Mideasem1Shmc)
|
abnormal mitosis
|
J:291786
|
Miftm1Gfr/Miftm1Gfr
(C57BL/6-Miftm1Gfr)
|
decreased fibroblast proliferation
|
J:147772
|
decreased mitotic index
|
J:84791
|
Miftm2Gfr/Miftm2Gfr
(C57BL/6-Miftm2Gfr)
|
decreased fibroblast proliferation
|
J:147772
|
Milr1tm1Shib/Milr1tm1Shib
(involves: C57BL/6N)
|
decreased mast cell degranulation
|
J:161854
|
Minute/Minute+
(involves: 101/H * C3H/HeH * C57BL/6J * CBA/Ca * M. spretus)
|
abnormal imprinting
|
J:75952
|
Minute/Minute+
(involves: 101/H * C3H/HeH)
|
abnormal imprinting
|
J:65007
|
Mir22tm1Boet/Mir22tm1Boet
(B6.129S2-Mir22tm1Boet)
|
increased fatty acid oxidation
|
J:266382
|
Mir24-1em1Smoc/Mir24-1em1Smoc Mir24-2em1Smoc/Mir24-2em1Smoc Tg(KRT14-cre)1Amc/0
(involves: C57BL/6J * CBA)
|
increased keratinocyte proliferation
|
J:306624
|
Mir26a-1em1Xfu/Mir26a-1em1Xfu Mir26a-2em1Xfu/Mir26a-2em1Xfu
(involves: C57BL/6)
|
increased pancreatic beta cell proliferation
|
J:286108
|
Mir32em1Gpt/Mir32em1Gpt Albem1(icre)Gpt/Alb+
(C57BL/6JGpt-Mir32em1Gpt Albem1(icre)Gpt)
|
decreased endoplasmic reticulum stress
|
J:344660
|
Mir34atm1.1Aven/Mir34atm1.1Aven
(involves: 129S4/SvJae * C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:180144
|
Mir34atm1.1Lhe/Mir34atm1.1Lhe
(involves: C57BL/6 * C57BL/6J)
|
abnormal cell physiology
|
J:180692
|
cellular phenotype
|
J:180692
|
Mir34atm1.1Lhe/Mir34atm1.1Lhe Mirc21tm1.1Lhe/Mirc21tm1.1Lhe
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J)
|
abnormal cell physiology
|
J:180692
|
cellular phenotype
|
J:180692
|
Mir34atm1.1Lhe/Mir34atm1.1Lhe Pou5f1tm2Jae/Pou5f1+
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J)
|
abnormal cell physiology
|
J:180692
|
Mir34atm1.1Pisc/Mir34atm1.1Pisc Mirc21tm1.1Pisc/Mirc21tm1.1Pisc Mirc34tm1.1Pisc/Mirc34tm1.1Pisc
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J)
|
abnormal oviduct epithelium motile cilium morphology
|
J:256929
|
decreased respiratory motile cilia number
|
J:256929
|
oligozoospermia
|
J:256929
|
Mir100em1Nju/Mir100em1Nju Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA)
|
increased hepatocyte karyomegaly
|
J:281439
|
Mir124a-1hgtm1Tfur/Mir124a-1hgtm1Tfur
(involves: 129S6/SvEvTac)
|
abnormal retina apoptosis
|
J:179784
|
increased neuron apoptosis
|
J:179784
|
Mir133a-1tm1.1Eno/Mir133a-1tm1.1Eno Mir133a-2tm1.1Eno/Mir133a-2tm1.1Eno
(involves: 129S/SvEv * C57BL/6 * SJL)
|
increased cardiomyocyte apoptosis
|
J:142220
|
Mir133a-1tm1Eno/Mir133a-1tm1Eno Mir133a-2tm1Eno/Mir133a-2tm1Eno
(involves: 129S/SvEv * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:142220
|
Mir139em1Jwli/Mir139em1Jwli
(C57BL/6J-Mir139em1Jwli)
|
abnormal enterocyte proliferation
|
J:280467
|
decreased enterocyte apoptosis
|
J:280467
|
Mir142tm1Teyo/Mir142tm1Teyo
(involves: C57BL/6)
|
decreased mast cell degranulation
|
J:211850
|
Mir142hgGt(IST11580H2)Tigm/Mir142hgGt(IST11580H2)Tigm
(involves: C57BL/6N)
|
abnormal dendritic cell differentiation
|
J:207516
|
Mir144/Mir451atm1.1Mjwe/Mir144/Mir451atm1.1Mjwe
(Not Specified)
|
increased cellular sensitivity to hydrogen peroxide
|
J:163250
|
Mir144/Mir451atm1.1Mjwe/Mir144/Mir451atm1.1Mjwe
(Not Specified)
|
increased cellular sensitivity to hydrogen peroxide
|
J:163250
|
Mir148atm2942.2Arte/Mir148atm2942.2Arte
(involves: C57BL/6 * FVB/N)
|
decreased cellular glucose uptake
|
J:307366
|
Mir149em1Ydw/Mir149em1Ydw
(C57BL/6J-Mir149em1Ydw)
|
increased hepatocyte apoptosis
|
J:294318
|
increased hepatocyte proliferation
|
J:294318
|
Mir155tm1Rsky/Mir155tm1Rsky
(involves: 129 * C57BL/6)
|
chromosomal instability
|
J:136224
|
Mir184tm1Ics/Mir184tm1Ics
(Not Specified)
|
increased pancreatic beta cell proliferation
|
J:210552
|
Mir185em1Smoc/Mir185em1Smoc
(Not Specified)
|
enhanced osteoblast differentiation
|
J:278853
|
increased osteoblast proliferation
|
J:278853
|
Mir188em1Xhl/Mir188em1Xhl
(C57BL/6-Mir188em1Xhl)
|
abnormal fat cell differentiation
|
J:222099
|
Mir195bem1Dfra/Mir195bem1Dfra
(Not Specified)
|
abnormal cell physiology
|
J:344186
|
Mir200btm1.1Osb/Mir200btm1.1Osb Mir429m1Osb/Mir429m1Osb
(involves: 129S2/SvPas * C57BL/6)
|
decreased oocyte number
|
J:199159
|
Mir202em1Hncs/Mir202em1Hncs
(involves: C57BL/6J * ICR)
|
abnormal chromosomal synapsis
|
J:338367
|
abnormal male meiosis
|
J:338367
|
abnormal synaptonemal complex
|
J:338367
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:338367
|
absent chiasmata formation
|
J:338367
|
arrest of male meiosis
|
J:338367
|
decreased male germ cell number
|
J:338367
|
increased male germ cell apoptosis
|
J:338367
|
multinucleated giant male germ cells
|
J:338367
|
oligozoospermia
|
J:338367
|
Mir214tm1.1Eno/Mir214tm1.1Eno
(involves: C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:184550
|
Mir223tm1Fcam/Mir223tm1Fcam
(involves: 129S4/SvJae * C57BL/6)
|
abnormal neutrophil differentiation
|
J:140009
|
Mir326em1Qiuj/Mir326em1Qiuj
(involves: C57BL/6)
|
decreased neuron apoptosis
|
J:354144
|
Mir378atm1.1Eno/Mir378atm1.1Eno
(involves: 129S/SvEv * C57BL/6)
|
abnormal mitochondrial physiology
|
J:190154
|
Mir425em1Nju/Mir425+
(involves: C57BL/6)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:280159
|
Mir503hgem1Jina/Mir503hgem1Jina
(C57BL/6J-Mir503hgem1Jina)
|
abnormal mitochondrial morphology
|
J:336590
|
Mir592em1Jzhan/Mir592em1Jzhan
(Not Specified)
|
impaired neuron differentiation
|
J:323615
|
increased neuron apoptosis
|
J:323615
|
Mir802em3Gpt/Mir802em3Gpt Tg(Ins2-cre)25Mgn/0
(involves: C57BL/6JGpt * DBA)
|
abnormal pancreatic beta cell differentiation
|
J:287584
|
Mirc1tm1.1Aven/Mirc1tm1.1Aven
(involves: 129S4/SvJae * C57BL/6 * SJL/J)
|
increased B cell apoptosis
|
J:223213
|
Mirc1tm1.1Tyj/Mirc1tm1.1Tyj Pkd1tm1.1Pcha/Pkd1tm2Som Tg(Cdh16-cre)91Igr/0
(involves: 129 * 129S4/SvJae * C57BL/6 * ICR)
|
abnormal peroxisome morphology
|
J:244067
|
abnormal redox activity
|
J:244067
|
decreased kidney cell proliferation
|
J:244067
|
increased fatty acid oxidation
|
J:244067
|
Mirc1tm1.1Tyj/Mirc1tm1.1Tyj Pkd1tm2Som/Pkd1tm2Som Tg(Cdh16-cre)91Igr/0
(involves: 129S4/SvJae * C57BL/6 * ICR)
|
decreased kidney cell proliferation
|
J:244067
|
Mirc1tm1.1Tyj/Mirc1tm1.1Tyj Pkd2tm3Som/Pkd2tm3Som Tg(Pkhd1-cre)1Igr/0
(involves: 129S4/SvJae * C57BL/6)
|
decreased kidney cell proliferation
|
J:244067
|
Mirc1tm1.2Tyj/Mirc1tm1.2Tyj
(involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL)
|
increased B cell apoptosis
|
J:134861
|
Mirc1tm1.3Tyj/Mirc1tm1.3Tyj
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
increased B cell apoptosis
|
J:134861
|
Mirc1tm1Tyj/Mirc1tm1Tyj Tg(Mx1-cre)1Cgn/0
(involves: 129S4/SvJae * C57BL/6 * CBA * SJL)
|
increased B cell apoptosis
|
J:134861
|
Mirc1tm2.1Aven/Mirc1tm2.1Aven Tg(IghMyc)22Bri/?
(involves: 129S4/SvJae * C57BL/6 * SJL/J)
|
increased B cell apoptosis
|
J:223213
|
Mirc1tm3.1Aven/Mirc1tm3.1Aven
(involves: 129S4/SvJae * C57BL/6 * SJL/J)
|
increased B cell apoptosis
|
J:223213
|
Mirc2tm1.1Tyj/Y Mirc3tm1.1Tyj/Mirc3tm1.1Tyj Mirc1tm1.2Tyj/Mirc1tm1.2Tyj
(involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL)
|
increased apoptosis
|
J:134861
|
Mirc3tm1.1Tyj/Mirc3tm1.1Tyj Mirc1tm1.2Tyj/Mirc1tm1.2Tyj
(involves: 129S4/SvJae * C57BL/6 * FVB/N * SJL)
|
increased apoptosis
|
J:134861
|
Mirc5tm1Jae/Mirc5tm1Jae
(involves: 129S4/SvJae * C57BL/6)
|
abnormal primordial germ cell migration
|
J:175228
|
decreased germ cell number
|
J:175228
|
decreased male germ cell number
|
J:175228
|
decreased oocyte number
|
J:175228
|
decreased primordial germ cell number
|
J:175228
|
Mirc6tm1.1Mzhu/Mirc6+
(B6.129(Cg)-Mirc6tm1.1Mzhu)
|
paternal imprinting
|
J:227271
|
Mirc13tm1Biat/Mirc13+ Mirc4tm1.1Biat/Mirc4tm1.1Biat Tg(Ins2-cre)23Herr/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
abnormal pancreatic beta cell apoptosis
|
J:314874
|
Mirc13tm1Biat/Mirc13tm1Biat
(involves: C57BL/6J * C57BL/6N)
|
abnormal pancreatic beta cell apoptosis
|
J:314874
|
Mirc13tm1Biat/Mirc13tm1Biat Mirc4tm1.1Biat/Mirc4tm1.1Biat Tg(Ins2-cre)23Herr/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
abnormal pancreatic beta cell apoptosis
|
J:314874
|
Mirc14tm1.2Flv/Mirc14tm1.2Flv
(involves: C57BL/6 * C57BL/6N * FVB/N * SJL)
|
decreased T cell proliferation
|
J:203157
|
decreased thymocyte apoptosis
|
J:203157
|
Mirc19tm1.1Kcho/Mirc19tm1.1Kcho
(B6.129-Mirc19tm1.1Kcho)
|
maternal effect
|
J:166674
|
Mirc20tm1.1Blel/Mirc20tm1.1Blel
(involves: 129S4/SvJae * C57BL/6)
|
increased brain apoptosis
|
J:232516
|
premature neuronal precursor differentiation
|
J:232516
|
Mirc21tm1.1Kry/Mirc21tm1.1Kry Tg(Col1a1-cre)1Kry/0
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * FVB/N)
|
enhanced osteoblast differentiation
|
J:185130
|
increased osteoblast proliferation
|
J:185130
|
Mirc21tm1.1Lhe/Mirc21tm1.1Lhe
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell physiology
|
J:180692
|
Mirc30tm1.2Rdf/Mirc30tm1.2Rdf
(involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6)
|
abnormal B cell proliferation
|
J:156946
|
Mirc33em1Smoc/Mirc33em1Smoc
(Not Specified)
|
abnormal exocytosis
|
J:324059
|
abnormal vesicle-mediated transport
|
J:324059
|
Mirc33tm1.1Wtsi/Mirc33tm1.1Wtsi
(C57BL/6N-Mirc33tm1.1Wtsi)
|
decreased mitochondrial size
|
J:267719
|
increased mitochondrial DNA content
|
J:267719
|
increased mitochondrial number
|
J:267719
|
Mirc33tm1.1Wtsi/Mirc33tm1.1Wtsi Ppargc1atm1Brsp/Ppargc1a+
(involves: 129S4/SvJae * C57BL/6N)
|
decreased mitochondrial size
|
J:267719
|
Mirc55tm1.1Eno/Mirc55tm1.1Eno
(Not Specified)
|
decreased vascular endothelial cell proliferation
|
J:139708
|
Mis18atm1.1Kiik/Mis18atm1.2Kiik
(B6(129S)-Mis18atm1.1Kiik/Mis18atm1.2Kiik)
|
abnormal mitosis
|
J:188023
|
decreased fibroblast proliferation
|
J:188023
|
Mis18atm1.2Kiik/Mis18atm1.2Kiik
(B6(129S)-Mis18atm1.2Kiik)
|
abnormal DNA methylation
|
J:188023
|
abnormal mitosis
|
J:188023
|
decreased inner cell mass proliferation
|
J:188023
|
increased embryonic tissue cell apoptosis
|
J:188023
|
Misfaem1Kei/Misfaem1Kei
(C57BL/6J-Misfaem1Kei)
|
asthenozoospermia
|
J:332977
|
kinked sperm flagellum
|
J:332977
|
Misfaem2Kei/Misfaem2Kei
(C57BL/6J-Misfaem2Kei)
|
asthenozoospermia
|
J:332977
|
Misfaem5Kei/Misfaem5Kei
(C57BL/6J-Misfaem5Kei)
|
abnormal sperm mitochondrial sheath morphology
|
J:332977
|
asthenozoospermia
|
J:332977
|
kinked sperm flagellum
|
J:332977
|
Misfadtem1Psv/Misfadtem1Psv
(C57BL/6-Misfadtem1Psv)
|
abnormal oocyte morphology
|
J:291605
|
Mispem2Nsas/Mispem2Nsas
(FVB/NJcl-Mispem2Nsas)
|
abnormal enterocyte proliferation
|
J:333842
|
decreased colon goblet cell number
|
J:333842
|
Mitfmi-bw/Mitfmi-bw Tg(Dct-lacZ)A12Jkn/0
(involves: C3H * C57BL/6 * C57BL/6J * CBA)
|
abnormal melanoblast migration
|
J:213982
|
MkksGt(OST367255)Lex/MkksGt(OST367255)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal inner hair cell kinocilium location or orientation
|
J:102697
|
Mkkstm1Vcs/Mkkstm1Vcs
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J))
|
absent sperm flagellum
|
J:99276
|
Mkrn2tm1.1Bhj/Mkrn2tm1.1Bhj
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal acrosome morphology
|
J:250191
|
abnormal outer dense fiber morphology
|
J:250191
|
abnormal sperm axoneme morphology
|
J:250191
|
abnormal sperm flagellum morphology
|
J:250191
|
abnormal sperm head morphology
|
J:250191
|
absent acrosome
|
J:250191
|
asthenozoospermia
|
J:250191
|
decreased male germ cell number
|
J:250191
|
decreased spermatid number
|
J:250191
|
oligozoospermia
|
J:250191
|
Mkrn3em1Rhu/Mkrn3+
(involves: C57BL/6)
|
maternal imprinting
|
J:305000
|
Mks1hlb614/Mks1hlb614
(involves: C3H * C57BL/6)
|
absent nodal flow
|
J:167534
|
decreased embryonic cilium length
|
J:167534
|
decreased embryonic cilium number
|
J:167534
|
decreased kidney epithelial cell primary cilium length
|
J:167534
|
Mks1krc/Mks1krc
(involves: C3HeB/FeJ * C57BL/6 * CD-1)
|
abnormal motile primary cilium morphology
|
J:154075
|
abnormal primary cilium morphology
|
J:154075
|
Mks1tm1a(EUCOMM)Wtsi/Mks1tm1a(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
abnormal cell morphology
|
J:196290
|
abnormal ependyma motile cilium morphology
|
J:196290
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:196290
|
increased cell proliferation
|
J:196290
|
increased kidney cell proliferation
|
J:196290
|
increased neuron apoptosis
|
J:196290
|
Mldhrem1Zhgn/Mldhrem1Zhgn
(involves: C57BL/6)
|
abnormal cell physiology
|
J:303725
|
abnormal tricarboxylic acid cycle
|
J:303725
|
increased cellular ATP level
|
J:303725
|
Mlf1tm1Swm/Mlf1tm1Swm
(involves: 129 * C57BL/6)
|
decreased splenocyte apoptosis
|
J:266833
|
Mlh1tm1Lisk/Mlh1tm1Lisk
(involves: 129S7/SvEvBrd)
|
arrest of male meiosis
|
J:34291
|
azoospermia
|
J:34291
|
Mlh1tm1Lisk/Mlh1tm1Lisk
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal chiasmata formation
|
J:216866
|
Mlh1tm1Rak/Mlh1tm1Rak
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal apoptosis
|
J:33878
|
abnormal female meiosis
|
J:33878
|
arrest of male meiosis
|
J:33878
|
azoospermia
|
J:33878
|
Mlh1tm1Rak/Mlh1tm1Rak
(involves: 129P2/OlaHsd)
|
decreased sensitivity to induced cell death
|
J:133352
|
Mlh1tm1Wed/Mlh1tm1Wed
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal male meiosis
|
J:133352
|
abnormal meiotic spindle morphology
|
J:133352
|
arrest of male meiosis
|
J:133352
|
oligozoospermia
|
J:133352
|
Mlh3tm1Lpkn/Mlh3tm1Lpkn
(involves: 129S/SvEv)
|
abnormal female meiosis
|
J:78200
|
abnormal male meiosis
|
J:78200
|
azoospermia
|
J:78200
|
Mlklem1Jhan/Mlklem1Jhan
(involves: C57BL/6)
|
decreased sensitivity to induced cell death
|
J:204622
|
Mlklm1Btlr/Mlkl+
(C57BL/6J-Mlklm1Btlr)
|
decreased cell death
|
J:225934
|
Mlklm1Btlr/Mlklm1Btlr
(C57BL/6J-Mlklm1Btlr)
|
decreased cell death
|
J:225934
|
Mlklm2Btlr/Mlkl+
(C57BL/6J-Mlklm2Btlr)
|
decreased cell death
|
J:234252
|
Mlklm2Btlr/Mlklm2Btlr
(C57BL/6J-Mlklm2Btlr)
|
decreased cell death
|
J:234252
|
Mlklm3Btlr/Mlkl+
(C57BL/6J-Mlklm3Btlr)
|
decreased cell death
|
J:234251
|
Mlklm3Btlr/Mlklm3Btlr
(C57BL/6J-Mlklm3Btlr)
|
decreased cell death
|
J:234251
|
MlklM4Btlr/MlklM4Btlr
(C57BL/6J-MlklM4Btlr)
|
decreased apoptosis
|
J:272831
|
Mlkltm1.2Wsa/Mlkltm1.2Wsa
(involves: BALB/cJ * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:204620
|
Mllt10tm1Saam/Mllt10tm1Saam Tg(Mx1-cre)1Cgn/?
(involves: 129 * C57BL/6J * CBA/J)
|
abnormal cell physiology
|
J:217454
|
Mllt11tm1c(KOMP)Mbp/Mllt11tm1c(KOMP)Mbp Cux2tm1.1(cre)Mull/Cux2+
(involves: C57BL/6 * C57BL/6J * C57BL/6N)
|
abnormal neuronal migration
|
J:324710
|
Mlxtm1.1Rne/Mlxtm1.1Rne Tg(Amh-cre)8815Reb/0
(involves: 129S4/SvJaeSor * FVB/N)
|
asthenozoospermia
|
J:324060
|
oligozoospermia
|
J:324060
|
teratozoospermia
|
J:324060
|
Mlxtm1.2Rne/Mlxtm1.2Rne
(involves: 129S4/SvJaeSor)
|
abnormal sperm progressive motility
|
J:324060
|
decreased male germ cell number
|
J:324060
|
oligozoospermia
|
J:324060
|
teratozoospermia
|
J:324060
|
Mlxiptm1.2Lchan/Mlxiptm1.2Lchan
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
increased fatty acid oxidation
|
J:217834
|
Mlxipltm1Kuy/Mlxipltm1Kuy
(involves: 129S6/SvEvTac * C57BL/6J)
|
asthenozoospermia
|
J:324060
|
immotile sperm
|
J:324060
|
MmachcGt(AZ0348)Wtsi/MmachcGt(AZ0348)Wtsi
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6)
|
decreased trophectoderm cell proliferation
|
J:212387
|
Mmdtm1Beij/Mmdtm1Beij
(Not Specified)
|
abnormal macrophage differentiation
|
J:304637
|
increased macrophage apoptosis
|
J:304637
|
Mmp7tm1Lmm/Mmp7tm1Lmm
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ)
|
impaired macrophage chemotaxis
|
J:124841
|
Mmp9tm1Tvu/Mmp9tm1Tvu
(involves: 129S6/SvEvTac * CD-1)
|
abnormal megakaryocyte differentiation
|
J:149957
|
abnormal retina apoptosis
|
J:129161
|
Mmp9tm1Tvu/Mmp9tm1Tvu
(involves: 129S6/SvEvTac * C57BL/6)
|
increased T cell proliferation
|
J:88065
|
Mmp9tm1Tvu/Mmp9tm1Tvu
(involves: 129S6/SvEvTac * FVB/N)
|
decreased neuron apoptosis
|
J:96548
|
Mmp9tm1Tvu/Mmp9tm1Tvu
(FVB.129S6(Cg)-Mmp9tm1Tvu/J)
|
abnormal intestinal goblet cell morphology
|
J:128322
|
Mmp9tm1Tvu/Mmp9tm1Tvu Tg(KRT14-HPV16)wt1Dh/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2 * FVB/N)
|
decreased keratinocyte proliferation
|
J:65699
|
Mmp13tm1Jdar/Mmp13tm1Jdar
(B6.129S-Mmp13tm1Jdar)
|
decreased cell proliferation
|
J:150790
|
Mmp13tm1Jdar/Mmp13tm1Jdar Mmp9tm1Tvu/Mmp9tm1Tvu
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N)
|
decreased cell proliferation
|
J:150790
|
Mmp14tm1Hbh/Mmp14tm1Hbh
(involves: 129P2/OlaHsd * Black Swiss)
|
impaired osteoblast differentiation
|
J:198679
|
Mmp14tm1Ski/Mmp14tm1Ski
(B6.Cg-Mmp14tm1Ski)
|
abnormal basement membrane morphology
|
J:165029
|
decreased kidney cell proliferation
|
J:165029
|
Mmp19tm1Rase/Mmp19tm1Rase
(B6.129P2-Mmp19tm1Rase)
|
decreased T cell proliferation
|
J:137128
|
Mmp24tm1Otin/Mmp24tm1Otin
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal axon extension
|
J:153230
|
abnormal mast cell degranulation
|
J:153230
|
increased mast cell degranulation
|
J:153230
|
Mmp28tm1Mani/Mmp28tm1Mani
(B6.129X1-Mmp28tm1Mani)
|
abnormal macrophage chemotaxis
|
J:145912
|
Mmuttm1Cpv/Mmuttm1Cpv
(involves: 129S/SvEv * C57BL/6 * FVB/N)
|
abnormal hepatocyte mitochondrial morphology
|
J:147313
|
abnormal respiratory electron transport chain
|
J:147313
|
abnormal tricarboxylic acid cycle
|
J:147313
|
Mmuttm1Cpv/Mmuttm1Cpv Tg(Alb-Mut)#Cpv/0
(involves: C57BL/6)
|
abnormal mitochondrial crista morphology
|
J:200689
|
abnormal mitochondrial matrix morphology
|
J:200689
|
oxidative stress
|
J:200689
|
Mnd1Gt(RRS590)Byg/Mnd1Gt(RRS590)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal male meiosis
|
J:207221
|
Mnd1Gt(RRS590)Byg/Mnd1Gt(RRS590)Byg Psmc3iptm1Rdco/Psmc3iptm1Rdco
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:207221
|
abnormal male meiosis
|
J:207221
|
Mns1tm1Jw/Mns1tm1Jw
(involves: 129S4/SvJae * C57BL/6)
|
abnormal outer dense fiber morphology
|
J:183398
|
abnormal respiratory motile cilium morphology
|
J:183398
|
abnormal sperm axoneme morphology
|
J:183398
|
abnormal sperm flagellum morphology
|
J:183398
|
abnormal sperm mitochondrial sheath morphology
|
J:183398
|
abnormal spermatid morphology
|
J:183398
|
absent sperm fibrous sheath
|
J:183398
|
immotile sperm
|
J:183398
|
kinked sperm flagellum
|
J:183398
|
oligozoospermia
|
J:183398
|
short sperm flagellum
|
J:183398
|
Mnttm1.1Phu/Mnttm1.1Phu
(Not Specified)
|
abnormal cell physiology
|
J:85481
|
Mnx1tm1Jhk/Mnx1tm1Jhk
(involves: 129S1/Sv)
|
abnormal axon guidance
|
J:89755
|
Mnx1tm1Jhk/Mnx1tm1Jhk Isl2tm2Slp/Isl2tm2Slp
(involves: 129P2/OlaHsd * 129S1/Sv)
|
abnormal axon guidance
|
J:89755
|
Moap1tm1Vcy/Moap1tm1Vcy
(B6.129-Moap1tm1Vcy)
|
decreased hepatocyte apoptosis
|
J:238373
|
Mob1atm1.1Asuz/Mob1atm1.1Asuz Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(B6.Cg-Mob1bGt(CC0690)Wtsi Mob1atm1.1Asuz Speer6-ps1Tg(Alb-cre)21Mgn)
|
increased hepatocyte proliferation
|
J:228499
|
Mob1atm1.1Asuz/Mob1atm1.1Asuz Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi Tg(KRT14-cre/ERT)20Efu/0
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
abnormal cell nucleus morphology
|
J:193981
|
abnormal mitosis
|
J:193981
|
abnormal mitotic spindle morphology
|
J:193981
|
decreased keratinocyte apoptosis
|
J:193981
|
increased keratinocyte proliferation
|
J:193981
|
Mob1atm1.2Asuz/Mob1atm1.2Asuz Mob1bGt(CC0690)Wtsi/Mob1bGt(CC0690)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:193981
|
abnormal mitosis
|
J:193981
|
absent inner cell mass proliferation
|
J:193981
|
Mocosem2(IMPC)Ics/Mocosem2(IMPC)Ics
(involves: C57BL/6N)
|
abnormal redox activity
|
J:336718
|
increased kidney cell proliferation
|
J:336718
|
increased renal tubule apoptosis
|
J:336718
|
Mocs2tm1(KOMP)Vlcg/Mocs2+
(involves: C57BL/6NTac)
|
increased neuron apoptosis
|
J:242197
|
Mocs2tm1(KOMP)Vlcg/Mocs2tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
increased neuron apoptosis
|
J:242197
|
ModmBALB/cByJ/ModmBALB/cByJ
(involves: BALB/cByJ * C57BL/6ByJ)
|
abnormal DNA methylation
|
J:67850
|
ModmC57BL/6ByJ/ModmC57BL/6ByJ
(involves: BALB/cByJ * C57BL/6ByJ)
|
abnormal DNA methylation
|
J:67850
|
Mogtm1Reid/Mogtm1Reid
(129/Sv-Mogtm1Reid)
|
increased T cell proliferation
|
J:86663
|
Mol1BALB/cByJ/Mol1BALB/cByJ
(involves: BALB/cByJ * C57BL/6ByJ)
|
decreased B cell proliferation
|
J:58921
|
Morc1Tg(Tyr)1Az/Morc1Tg(Tyr)1Az
(FVB/NHsd-Morc1Tg(Tyr)1Az)
|
abnormal apoptosis
|
J:51211
|
arrest of male meiosis
|
J:51211
|
azoospermia
|
J:51211
|
decreased male germ cell number
|
J:51211
|
Morc2aem1Snupy/Morc2a+
(involves: C57BL/6)
|
increased neuron apoptosis
|
J:341847
|
Morc2btm1Jw/Morc2btm1Jw
(involves: 129S4/SvJae * C57BL/6)
|
abnormal chromosomal synapsis
|
J:256987
|
abnormal double-strand DNA break repair
|
J:256987
|
abnormal female meiosis
|
J:256987
|
abnormal meiosis
|
J:256987
|
absent oocytes
|
J:256987
|
arrest of male meiosis
|
J:256987
|
azoospermia
|
J:256987
|
increased female germ cell apoptosis
|
J:256987
|
increased male germ cell apoptosis
|
J:256987
|
Morf4l1tm1Kto/Morf4l1tm1Kto
(involves: 129S7/SvEvBrd)
|
decreased cell proliferation
|
J:97640
|
Mostm1Ev/Mostm1Ev
(involves: 129S/SvEv)
|
abnormal female meiosis
|
J:19118
|
abnormal meiotic spindle morphology
|
J:19118,
J:110272
|
abnormal polar body morphology
|
J:19118
|
Mostm1Gvw/Mostm1Gvw
(involves: 129S1/Sv)
|
abnormal female meiosis
|
J:34085
|
abnormal meiotic spindle morphology
|
J:34085
|
abnormal primary polar body morphology
|
J:34085
|
parthenogenesis
|
J:34085
|
Mostm1Sia/Mostm1Sia
(involves: C57BL/6 * CBA)
|
abnormal female meiosis
|
J:19086
|
Mov10l1tm1.2Eno/Mov10l1tm1.2Eno
(involves: 129S/SvEv * C57BL/6)
|
abnormal male meiosis
|
J:161124
|
abnormal spermatocyte morphology
|
J:161124
|
arrest of male meiosis
|
J:161124
|
azoospermia
|
J:161124
|
decreased elongated spermatid number
|
J:161124
|
increased male germ cell apoptosis
|
J:161124
|
Mov10l1tm1.2Jw/Mov10l1tm1.2Jw
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal DNA methylation during gametogenesis
|
J:161125
|
abnormal male meiosis
|
J:161125
|
arrest of male meiosis
|
J:161125
|
azoospermia
|
J:161125
|
Mp/Mp
(involves: 101/Rl * C3H/Rl * C57BL/6J * CBA)
|
abnormal endoplasmic reticulum morphology
|
J:203031
|
Mp/Mp
(involves: 101/Rl * C3H/Rl * C57BL/6J * CBA * CD-1)
|
abnormal endoplasmic reticulum morphology
|
J:203031
|
Mpc1tm1c(EUCOMM)Wtsi/Mpc1tm1c(EUCOMM)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * C57BL/6J * C57BL/6N * DBA)
|
abnormal mitochondrial physiology
|
J:236662
|
increased fatty acid oxidation
|
J:236662
|
Mpc2em2Finc/Mpc2em2Finc
(involves: C57BL/6)
|
abnormal mitochondrial physiology
|
J:211781
|
Mpgtm1Lds/Mpgtm1Lds
(involves: 129P2/OlaHsd * C57BL/6)
|
increased apoptosis
|
J:118148
|
Mpgtm1Rhe/Mpgtm1Rhe
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal pancreatic islet cell apoptosis
|
J:70603
|
MpiGt(OST90588)Lex/MpiGt(OST90588)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:109220
|
abnormal cell proliferation
|
J:109220
|
increased embryonic tissue cell apoptosis
|
J:109220
|
Mpig6btm1.1Arte/Mpig6btm1.1Arte
(involves: C57BL/6NTac)
|
abnormal megakaryocyte differentiation
|
J:201266
|
decreased platelet ATP level
|
J:201266
|
Mpltm1Wsa/Mpltm1Wsa MybPlt3/Myb+
(involves: 129S1/Sv * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:89601
|
Mpltm1Wsa/Mpltm1Wsa MybPlt3/MybPlt3
(involves: 129S1/Sv * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:89601
|
Mpltm1Wsa/Mpltm1Wsa MybPlt4/Myb+
(involves: 129S1/Sv * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:89601
|
Mpltm1Wsa/Mpltm1Wsa MybPlt4/MybPlt4
(involves: 129S1/Sv * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:89601
|
Mpltm1Wsa/Mpltm1Wsa Suz12Plt8/Suz12+
(B6.Cg-Mpltm1Wsa Suz12Plt8)
|
abnormal megakaryocyte differentiation
|
J:136262
|
Mpltm2.1Wsa/Mpltm2.1Wsa Tg(Pf4-icre)Q3Rsko/0
(involves: C57BL/6)
|
increased hematopoietic stem cell proliferation
|
J:208120
|
Mpp1tm1Ahc/Mpp1tm1Ahc
(B6.129-Mpp1tm1Ahc)
|
impaired neutrophil chemotaxis
|
J:154749
|
Mpp3tm1.1Wij/Mpp3tm1.1Wij Emx1tm1(cre)Ito/Emx1+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
abnormal mitotic spindle morphology
|
J:198427
|
abnormal neuronal migration
|
J:198427
|
increased mitotic index
|
J:198427
|
Mpp4tm1Wij/Mpp4tm1Wij
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal plasma membrane morphology
|
J:108232
|
Mpsttm1Nori/Mpst+ Tg(CAG-cre)13Miya/0
(involves: C57BL/6 * C57BL/6JJcl)
|
abnormal spermatocyte morphology
|
J:207803
|
Mpv17/Mpv17
(CFW-Mpv17/J)
|
abnormal mitochondrial crista morphology
|
J:143355
|
cellular phenotype
|
J:143355
|
decreased hepatocyte mitochondrial DNA content
|
J:143355
|
decreased mitochondrial DNA content
|
J:143355
|
decreased muscle fiber mitochondrial DNA content
|
J:143355
|
dilated mitochondrion
|
J:143355
|
Mpztm1Msch/Mpz+
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal macrophage chemotaxis
|
J:67581
|
Mpztm3.1Wra/Mpz+
(FVB.129S2(Cg)-Mpztm3.1Wra)
|
increased Schwann cell proliferation
|
J:241742
|
Mpztm3.1Wra/Mpztm3.1Wra
(FVB.129S2(Cg)-Mpztm1.1Wra)
|
increased endoplasmic reticulum stress
|
J:241742
|
increased Schwann cell proliferation
|
J:241742
|
Mrc2tm1Cmi/Mrc2tm1Cmi
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
decreased fibroblast cell migration
|
J:124909
|
Mre11atm1.1Rchd/Mre11atm1.1Rchd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:184053
|
chromosomal instability
|
J:184053
|
increased mitotic index
|
J:184053
|
Mre11atm1Dof/Mre11atm2.1Dof
(involves: 129S6/SvEvTac)
|
abnormal DNA repair
|
J:147247
|
cellular phenotype
|
J:147247
|
chromosomal instability
|
J:147247
|
decreased cell proliferation
|
J:147247
|
increased cellular sensitivity to ionizing radiation
|
J:147247
|
induced chromosome breakage
|
J:147247
|
Mre11atm1Jpt/Mre11atm1Jpt
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:87088,
J:103922
|
chromosomal instability
|
J:87088
|
chromosome breakage
|
J:103922
|
increased cellular sensitivity to ionizing radiation
|
J:87088,
J:103922
|
induced chromosome breakage
|
J:87088
|
maternal effect
|
J:87088
|
Mre11atm1Jpt/Mre11atm1Jpt
(involves: 129S7/SvEvBrd)
|
decreased cellular sensitivity to ionizing radiation
|
J:144172
|
Mre11atm1Jpt/Mre11atm1Jpt Rad50tm2Jpt/Rad50tm2Jpt
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:103922
|
chromosome breakage
|
J:103922
|
increased cellular sensitivity to ionizing radiation
|
J:103922
|
Mre11atm2.1Dof/Mre11atm2.2Dof
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:147247
|
abnormal DNA repair
|
J:147247
|
chromosomal instability
|
J:147247
|
decreased cell proliferation
|
J:147247
|
increased cellular sensitivity to ionizing radiation
|
J:147247
|
induced chromosome breakage
|
J:147247
|
spontaneous chromosome breakage
|
J:147247
|
Mrgprb2em1Xzd/Mrgprb2em1Xzd
(C57BL/6-Mrgprb2em1Xzd)
|
decreased mast cell degranulation
|
J:219209
|
Mrnipem1Nju/Mrnipem1Nju
(involves: CD-1)
|
abnormal chromosomal synapsis
|
J:305295
|
abnormal male meiosis
|
J:305295
|
asthenozoospermia
|
J:305295
|
oligozoospermia
|
J:305295
|
Mrpl3em1(IMPC)J/Mrpl3em1(IMPC)J
(C57BL/6N-Mrpl3em1(IMPC)J/Mmucd)
|
abnormal cell cycle checkpoint function
|
J:290315
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:290315
|
abnormal mitochondrial crista morphology
|
J:290315
|
abnormal mitochondrial morphology
|
J:290315
|
abnormal mitochondrial physiology
|
J:290315
|
abnormal respiratory electron transport chain
|
J:290315
|
cellular phenotype
|
J:290315
|
decreased cellular ATP level
|
J:290315
|
Mrpl12em1Smoc/Mrpl12em1Smoc Tg(Cdh16-cre)91Igr/0
(involves: C57BL/6 * ICR)
|
abnormal mitochondrial crista morphology
|
J:339098
|
abnormal mitochondrial morphology
|
J:339098
|
dilated mitochondrion
|
J:339098
|
Mrpl22tm1b(KOMP)Mbp/Mrpl22tm1b(KOMP)Mbp
(C57BL/6N-Atm1Brd Mrpl22tm1b(KOMP)Mbp/JMmucd)
|
abnormal cell cycle checkpoint function
|
J:290315
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:290315
|
abnormal mitochondrial crista morphology
|
J:290315
|
abnormal mitochondrial morphology
|
J:290315
|
abnormal mitochondrial physiology
|
J:290315
|
abnormal respiratory electron transport chain
|
J:290315
|
cellular phenotype
|
J:290315
|
decreased cellular ATP level
|
J:290315
|
Mrpl44em1(IMPC)J/Mrpl44em1(IMPC)J
(C57BL/6N-Mrpl44em1(IMPC)J/Mmucd)
|
abnormal cell cycle checkpoint function
|
J:290315
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:290315
|
abnormal mitochondrial crista morphology
|
J:290315
|
abnormal mitochondrial morphology
|
J:290315
|
abnormal mitochondrial physiology
|
J:290315
|
abnormal respiratory electron transport chain
|
J:290315
|
cellular phenotype
|
J:290315
|
decreased cellular ATP level
|
J:290315
|
Mrps12em1.2Afi/Mrps12em1.2Afi
(B6N(Cg)-Mrps12em1.2Afi)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:284101
|
abnormal translation
|
J:284101
|
increased hepatocyte proliferation
|
J:284101
|
increased mitochondrial DNA content
|
J:284101
|
Mrps12em2.2Afi/Mrps12em2.2Afi
(B6N(Cg)-Mrps12em2.2Afi)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:284101
|
abnormal mitochondrial physiology
|
J:284101
|
abnormal translation
|
J:284101
|
cellular phenotype
|
J:284101
|
Mrps18ctm1.1(KOMP)Vlcg/Mrps18ctm1.1(KOMP)Vlcg
(C57BL/6N-Mrps18ctm1.1(KOMP)Vlcg/JMmucd)
|
abnormal cell cycle checkpoint function
|
J:290315
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:290315
|
abnormal mitochondrial crista morphology
|
J:290315
|
abnormal mitochondrial morphology
|
J:290315
|
abnormal mitochondrial physiology
|
J:290315
|
abnormal respiratory electron transport chain
|
J:290315
|
cellular phenotype
|
J:290315
|
decreased cellular ATP level
|
J:290315
|
Mrps22tm1.1(KOMP)Vlcg/Mrps22tm1.1(KOMP)Vlcg
(C57BL/6N-Mrps22tm1.1(KOMP)Vlcg/JMmucd)
|
abnormal cell cycle checkpoint function
|
J:290315
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:290315
|
abnormal mitochondrial crista morphology
|
J:290315
|
abnormal mitochondrial morphology
|
J:290315
|
abnormal mitochondrial physiology
|
J:290315
|
abnormal respiratory electron transport chain
|
J:290315
|
cellular phenotype
|
J:290315
|
decreased cellular ATP level
|
J:290315
|
Mrps34m1Anu/Mrps34m1Anu
(C57BL/6J-Mrps34m1Anu)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:222643
|
abnormal ribosome morphology
|
J:222643
|
abnormal translation
|
J:222643
|
Mrs2em1Muma/Mrs2em1Muma
(B6.Cg-Mrs2em1Muma)
|
abnormal mitochondrial physiology
|
J:298361
|
abnormal mitochondrial shape
|
J:298361
|
abnormal redox activity
|
J:298361
|
increased mitochondrial number
|
J:298361
|
Mrtfatm1Eno/Mrtfatm1Eno Mrtfbtm2.1Eno/Mrtfbtm2.1Eno Tg(GFAP-cre)25Mes/0
(involves: 129 * 129S/SvEv * C57BL/6 * FVB/N)
|
abnormal neuron differentiation
|
J:161853
|
abnormal neuronal migration
|
J:161853
|
impaired fibroblast cell migration
|
J:161853
|
increased neuron apoptosis
|
J:161853
|
Mrtfatm1Swm/Mrtfatm1Swm
(involves: 129/Sv * C57BL/6)
|
abnormal mitochondrial morphology
|
J:111560
|
abnormal muscle fiber mitochondrial morphology
|
J:111560
|
MrtfbGt(RRJ478)Byg/MrtfbGt(RRJ478)Byg
(involves: 129P2/OlaHsd)
|
impaired cardiac neural crest cell differentiation
|
J:160964
|
Mrtfbtm1.1Msp/Mrtfbtm1.1Msp
(involves: 129)
|
abnormal cell adhesion
|
J:187713
|
Ms4a7em1.1Jddl/Ms4a7em1.1Jddl
(B6.Cg-Ms4a7em1.1Jddl)
|
decreased hepatocyte apoptosis
|
J:347975
|
Msgn1tm1Wb/Msgn1tm1Wb
(involves: 129S1/Sv * C57BL/6)
|
increased tail bud apoptosis
|
J:66514
|
Msh2tm1Rak/Msh2tm1Rak Xpctm1Ecf/Xpctm1Ecf
(involves: 129P2/OlaHsd * SKH1)
|
abnormal cell cycle
|
J:94447
|
increased cellular sensitivity to ultraviolet irradiation
|
J:94447
|
Msh2tm1Rak/Msh2tm2.1Rak Tg(Vil1-cre)20Syr/0
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2 * SJL)
|
abnormal mismatch repair
|
J:161577
|
Msh2tm1Tts/Msh2tm1Tts Nudt1tm1Tts/Nudt1tm1Tts
(involves: 129S/SvEv * C57BL/6J)
|
abnormal cell physiology
|
J:79732
|
Msh2tm1Wed/Msh2tm1Wed
(involves: 129 * C57BL/6 * SJL)
|
abnormal mismatch repair
|
J:88092
|
Msh2tm2.1Rak/Msh2tm2.1Rak Tg(Vil1-cre)20Syr/0
(involves: 129/Sv * C57BL/6 * FVB/N * SJL)
|
abnormal mismatch repair
|
J:161577
|
Msh2tm2.1Rak/Msh2tm3.1Rak Tg(Vil1-cre)20Syr/0
(involves: 129/Sv * C57BL/6 * DBA/2 * SJL)
|
abnormal mismatch repair
|
J:161577
|
Msh2tm2.2Rak/Msh2tm2.2Rak
(involves: 129/Sv * C57BL/6 * FVB/N * SJL)
|
abnormal mismatch repair
|
J:161577
|
Msh3tm1Rak/Msh3tm1Rak
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal mismatch repair
|
J:60604
|
Msh3tm1Rak/Msh3tm1Rak Msh6tm1Rak/Msh6tm1Rak
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal mismatch repair
|
J:60604
|
Msh4tm1Wed/Msh4tm1Wed
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal female meiosis
|
J:62204
|
abnormal male meiosis
|
J:62204
|
azoospermia
|
J:62204
|
decreased germ cell number
|
J:62204
|
Msh4tm1Wed/Msh4tm1Wed Msh5tm1Rak/Msh5tm1Rak
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal male meiosis
|
J:62204
|
Msh5em1Jzc/Msh5em1Jzc
(involves: C57BL/6)
|
absent oocytes
|
J:241778
|
Msh5tm1Htr/Msh5tm1Htr
(involves: 129P2/OlaHsd * FVB)
|
abnormal female meiosis
|
J:53516
|
abnormal synaptonemal complex
|
J:180025
|
absent oocytes
|
J:53516
|
arrest of male meiosis
|
J:53516
|
azoospermia
|
J:53516
|
increased male germ cell apoptosis
|
J:53516
|
Msh5tm1Rak/Msh5tm1Rak
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal female meiosis
|
J:51921
|
abnormal male meiosis
|
J:51921,
J:62204
|
azoospermia
|
J:51921
|
decreased oocyte number
|
J:51921
|
Msi1tm1Okn/Msi1tm1Okn
(involves: C57BL/6 * ICR)
|
increased retina apoptosis
|
J:146380
|
Msmpem1Jzx/Msmpem1Jzx
(C57BL/6-Msmpem1Jzx)
|
abnormal macrophage differentiation
|
J:311042
|
Msntm1Sts/Y
(involves: 129S4/SvJae * C57BL/6)
|
impaired leukocyte migration
|
J:189837
|
Msratm1Jmo/Msratm1Jmo
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:72532
|
Msrb1Gt(OST336894)Lex/Msrb1Gt(OST336894)Lex
(involves: 129S5/SvEvBrd)
|
oxidative stress
|
J:147916
|
Msrb3tm1Hyk/Msrb3tm1Hyk
(involves: 129 * C57BL/6)
|
cellular phenotype
|
J:206322
|
increased apoptosis
|
J:206322
|
Mss51tm1(KOMP)Vlcg/Mss51tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal mitochondrial crista morphology
|
J:280597
|
abnormal mitochondrial morphology
|
J:280597
|
abnormal mitochondrial physiology
|
J:280597
|
abnormal mitochondrial shape
|
J:280597
|
increased mitochondrial DNA content
|
J:280597
|
Mstntm1.1Mgs/Mstntm1.1Mgs
(involves: 129S1/Sv * 129X1/SvJ * C57BL * FVB/N)
|
oxidative stress
|
J:184622
|
Mt1tm1Bri/Mt1tm1Bri Mt2tm1Bri/Mt2tm1Bri
(involves: 129S7/SvEvBrd)
|
increased brain apoptosis
|
J:53929
|
increased neuron apoptosis
|
J:103102
|
increased sensitivity to induced cell death
|
J:33276
|
oxidative stress
|
J:103102
|
Mt1tm1Bri/Mt1tm1Bri Mt2tm1Bri/Mt2tm1Bri
(129S7/SvEvBrd-Mt1tm1Bri Mt2tm1Bri/J)
|
decreased hepatocyte proliferation
|
J:109814
|
increased neuron apoptosis
|
J:89429
|
increased renal tubule apoptosis
|
J:126620
|
increased thymocyte apoptosis
|
J:57169
|
mt-Co1m1Jiha
(B6.Cg-mt-Co1m1Jiha)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:132960
|
mt-Co1m1Jiha
(involves: C57BL/6J * M. m. domesticus)
|
cardiac interstitial fibrosis
|
J:132659
|
mt-Co1m1Jiha mt-Nd6m1Dwa mt-Nd6m2Dwa
(involves: C3H/An * C57BL/6J * M. m. domesticus)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:132659
|
mt-Nd2m1
(ALR/Lt)
|
abnormal cellular respiration
|
J:117602
|
mt-Nd6m1Dwa
(involves: C3H/An * C57BL/6J * M. m. domesticus)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:132659
|
mt-Nd6m1Jbst mt-Tam1Jbst
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl)
|
abnormal mitochondrial physiology
|
J:238994
|
abnormal respiratory electron transport chain
|
J:238994
|
abnormal translation
|
J:238994
|
mt-Nd6m2Jiha
(involves: C3H/An * C57BL/6 * C57BL/6J * CBA)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:164405
|
mt-Nd6m3Dwa
(B6.129S-mt-Nd6m3Dwa)
|
abnormal cellular respiration
|
J:192260
|
abnormal mitochondrial morphology
|
J:192260
|
abnormal mitochondrial physiology
|
J:192260
|
abnormal respiratory electron transport chain
|
J:192260
|
increased mitochondrial fission
|
J:192260
|
mt-Tkm1
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal respiratory electron transport chain
|
J:206827
|
absent oocytes
|
J:206827
|
mt-Tl1m1Jiha
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal mitochondrial crista morphology
|
J:344247
|
abnormal mitochondrial physiology
|
J:344247
|
decreased mitochondrial size
|
J:344247
|
Mta1tm1Raku/Mta1tm1Raku
(involves: 129S4/SvJae)
|
increased cellular sensitivity to ionizing radiation
|
J:153679
|
Mta2tm1.1Yzha/Mta2tm1.1Yzha
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
increased kidney cell proliferation
|
J:137101
|
increased mesangial cell number
|
J:137101
|
increased T cell proliferation
|
J:137101
|
Mta2tm1Yzha/Mta2tm1Yzha Tg(Lck-cre)#Zhu/0
(involves: 129S4/SvJae * C57BL/6 * SJL)
|
increased T cell proliferation
|
J:137101
|
Mtdhtm1.2Dsar/Mtdhtm1.2Dsar
(either: B6.129(FVB)-Mtdhtm1.2Dsar or (129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N))
|
decreased macrophage proliferation
|
J:216688
|
Mterf1atm1.2Lrsn/Mterf1atm1.2Lrsn Mterf1btm1Lrsn/Mterf1btm1Lrsn
(B6N.Cg-Mterf1atm1.2Lrsn Mterf1btm1Lrsn)
|
abnormal cell physiology
|
J:198969
|
Mterf2Gt(OST453159)Lex/Mterf2Gt(OST453159)Lex
(B6.129S5-Mterf2Gt(OST453159)Lex)
|
abnormal cellular respiration
|
J:149828
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:149828
|
abnormal tricarboxylic acid cycle
|
J:149828
|
increased mitochondrial DNA content
|
J:149828
|
increased mitochondrial number
|
J:149828
|
increased mitochondrial size
|
J:149828
|
increased skeletal muscle fiber mitochondrial DNA content
|
J:149828
|
Mterf3tm1.1Lrsn/Mterf3tm1.1Lrsn Tg(Ckmm-cre)5Khn/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB * SJL)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:145125
|
abnormal mitochondrial physiology
|
J:145125
|
Mterf4tm1.1Lrsn/Mterf4tm1.1Lrsn Tg(Ckmm-cre)5Khn/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)
|
abnormal mitochondrial physiology
|
J:175816
|
Mtf1tm1Wsc/Mtf1tm1Wsc
(involves: 129 * C57BL/6)
|
increased cellular sensitivity to alkylating agents
|
J:48216
|
Mtf2Gt(U3Betageo)1Ruiz/Mtf2Gt(U3Betageo)1Ruiz
(involves: 129S2/SvPas)
|
delayed cellular replicative senescence
|
J:170279
|
Mtf2tm1.1Hko/Mtf2tm1.1Hko
(B6.Cg-Mtf2tm1.1Hko)
|
delayed cellular replicative senescence
|
J:170279
|
Mtf2tm1.1Hko/Mtf2tm1.1Hko Phc2tm1Hko/Phc2tm1Hko
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
early cellular replicative senescence
|
J:170279
|
Mtfmtem1Heb/Mtfmt+
(C57BL/6-Mtfmtem1Heb)
|
dilated mitochondrion
|
J:334467
|
Mtfmtem1Heb/Mtfmtem1Heb
(C57BL/6-Mtfmtem1Heb)
|
abnormal mitochondrial physiology
|
J:334467
|
abnormal mitochondrial shape
|
J:334467
|
dilated mitochondrion
|
J:334467
|
Mtfp1tm1.2Wait/Mtfp1tm1.2Wait Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6N * FVB/N)
|
abnormal mitochondrial physiology
|
J:330965
|
increased cardiomyocyte apoptosis
|
J:330965
|
Mtfr1Gt(OST6261)Lex/Mtfr1Gt(OST6261)Lex
(involves: 129S5/SvEvBrd)
|
increased cellular sensitivity to oxidative stress
|
J:124333
|
Mtfr1Gt(OST6261)Lex/Mtfr1Gt(OST6261)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:184121
|
Mtg1em1Ywxu/Mtg1em1Ywxu
(Not Specified)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:271147
|
Mthfd1tm1.1Rzn/Mthfd1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)
|
abnormal cell physiology
|
J:199578
|
maternal effect
|
J:199578
|
Mtlnem1Rlbd/Mtlnem1Rlbd
(involves: C57BL/6J * SJL/J)
|
abnormal oxidative phosphorylation
|
J:263464
|
decreased fatty acid beta-oxidation
|
J:263464
|
Mtm1Gt(OST290577)Lex/Y
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal mitochondrial physiology
|
J:192845
|
impaired autophagy
|
J:192845
|
oxidative stress
|
J:192845
|
Mtm1tm1.1Jman/Y
(involves: 129T1/Sv * C57BL/6)
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:81791
|
Mtmr14tm1Ckq/Mtmr14tm1Ckq
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal sperm head morphology
|
J:267733
|
abnormal sperm midpiece morphology
|
J:267733
|
abnormal sperm principal piece morphology
|
J:267733
|
asthenozoospermia
|
J:267733
|
decreased male germ cell number
|
J:267733
|
hairpin sperm flagellum
|
J:267733
|
increased male germ cell apoptosis
|
J:267733
|
short sperm flagellum
|
J:267733
|
teratozoospermia
|
J:267733
|
Mto1Gt(G019A03)Wrst/Mto1Gt(G019A03)Wrst
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal mitochondrial inner membrane morphology
|
J:223246
|
abnormal mitochondrial physiology
|
J:223246
|
decreased myocardial fiber mitochondrial DNA content
|
J:223246
|
MtorGt(OST92090)Lex/MtorGt(OST92090)Lex
(involves: 129S5/SvEvBrd)
|
absent inner cell mass proliferation
|
J:137592
|
Mtortm1.1Gcon/Mtortm1.1Gcon A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
abnormal autophagy
|
J:163763
|
abnormal mitochondrial physiology
|
J:163763
|
abnormal translation
|
J:163763
|
cardiac interstitial fibrosis
|
J:163763
|
dilated mitochondrion
|
J:163763
|
increased cardiomyocyte apoptosis
|
J:163763
|
Mtortm1.1Seq/Mtortm1.2Seq Tg(Nphs2-cre)1Seq/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal cell morphology
|
J:184667
|
Mtortm1.2Koz/Mtortm1.2Koz Tg(ACTA1-cre)79Jme/?
(involves: 129S4/SvJae * C57BL/6J * SJL)
|
decreased mitochondrial number
|
J:162918
|
Mtortm1.2Koz/Mtortm1.2Koz Tg(Cd4-cre)1Cwi/0
(involves: 129S4/SvJae * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:150108
|
Mtortm1Lgm/Mtortm1Lgm
(involves: 129S1/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:168600
|
decreased splenocyte apoptosis
|
J:168600
|
decreased splenocyte proliferation
|
J:168600
|
impaired B cell migration
|
J:168600
|
Mtortm1Yam/Mtortm1Yam
(involves: 129S4/SvJae)
|
absent inner cell mass proliferation
|
J:92252
|
Mtss1Gt(CSC156)Byg/Mtss1Gt(CSC156)Byg
(B6.129P2-Mtss1Gt(CSC156)Byg)
|
abnormal cell adhesion
|
J:174444
|
abnormal cell morphology
|
J:174444
|
abnormal cell physiology
|
J:174444
|
impaired fibroblast cell migration
|
J:174444
|
Mtss1Gt(RRI034)Byg/Mtss1Gt(RRI034)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased kidney cell proliferation
|
J:158762
|
Mtus1Gt(RRA048)Byg/Mtus1Gt(RRA048)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell morphology
|
J:212144
|
increased cell proliferation
|
J:212144
|
Muc2eey/Muc2eey
(C57BL/6-Muc2eey)
|
abnormal endoplasmic reticulum morphology
|
J:194148
|
abnormal enterocyte proliferation
|
J:194148
|
abnormal intestinal goblet cell morphology
|
J:194148
|
abnormal mitochondrial crista morphology
|
J:194148
|
dilated mitochondrion
|
J:194148
|
increased endoplasmic reticulum stress
|
J:194148
|
increased enterocyte apoptosis
|
J:194148
|
Muc2tm1Avel/Muc2tm1Avel
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell migration
|
J:75047
|
abnormal cell physiology
|
J:75047
|
abnormal enterocyte proliferation
|
J:75047
|
abnormal intestinal goblet cell morphology
|
J:75047
|
decreased enterocyte apoptosis
|
J:75047
|
increased cell proliferation
|
J:75047
|
Muc2wnn/Muc2+
(C57BL/6-Muc2wnn)
|
abnormal intestinal goblet cell morphology
|
J:194148
|
Muc2wnn/Muc2wnn
(C57BL/6-Muc2wnn)
|
abnormal endoplasmic reticulum morphology
|
J:194148
|
abnormal enterocyte proliferation
|
J:194148
|
abnormal intestinal goblet cell morphology
|
J:194148,
J:104190
|
abnormal mitochondrial crista morphology
|
J:194148
|
dilated mitochondrion
|
J:194148
|
increased endoplasmic reticulum stress
|
J:194148
|
increased enterocyte apoptosis
|
J:194148
|
Muc5actm1.1Evns/Muc5actm1.1Evns
(B6.129S1-Muc5actm1.1Evns)
|
abnormal intestinal goblet cell morphology
|
J:177306
|
Muc5btm1.2Evns/Muc5btm1.2Evns
(B6.129S1-Muc5btm1.2Evns)
|
impaired macrophage phagocytosis
|
J:207159
|
increased macrophage apoptosis
|
J:207159
|
Muc13tm1.1Mamg/Muc13tm1.1Mamg
(involves: 129 * C57BL/6)
|
abnormal enterocyte proliferation
|
J:313870
|
abnormal intestinal goblet cell physiology
|
J:313870
|
increased enterocyte apoptosis
|
J:313870
|
Mus81tm1Chmg/Mus81tm1Chmg
(involves: 129S4/SvJae * 129S5/SvEvBrd * C57BL/6)
|
decreased cell proliferation
|
J:100407
|
Mus81tm1Chmg/Mus81tm1Chmg
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal DNA repair
|
J:204996
|
increased sensitivity to induced cell death
|
J:204996
|
Mus81tm1Chmg/Mus81tm1Chmg Slx1btm1.1Jrou/Slx1btm1.1Jrou
(involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6)
|
abnormal DNA repair
|
J:204996
|
increased sensitivity to induced cell death
|
J:204996
|
Mus81tm1Raz/Mus81+
(involves: 129P2/OlaHsd)
|
chromosome breakage
|
J:91570
|
Mus81tm1Raz/Mus81tm1Raz
(involves: 129P2/OlaHsd)
|
chromosome breakage
|
J:91570
|
Musktm1.1Vwi/Musktm2Vwi
(Not Specified)
|
abnormal axon extension
|
J:141024
|
Musktm1.2Ics/Musktm1.2Ics
(involves: BALB/cN * C57BL/6NTac)
|
abnormal axon extension
|
J:221340
|
Mutyhtm1Yun/Mutyhtm1Yun
(involves: 129 * C57BL/6JJcl)
|
decreased susceptibility to neuronal excitotoxicity
|
J:193978
|
Mutyhtm1Yun/Mutyhtm1Yun Ogg1tm1Yun/Ogg1tm1Yun
(involves: 129S/SvEv * C57BL/6JJcl)
|
decreased susceptibility to neuronal excitotoxicity
|
J:193978
|
Mxd3tm1Rne/Mxd3tm1Rne
(either: 129S4/SvJaeSor or (involves: 129S4/SvJaeSor * C57BL/6J))
|
increased cellular sensitivity to gamma-irradiation
|
J:77649
|
Mxi1tm1Rdp/Mxi1tm1Rdp
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal cell physiology
|
J:48236
|
increased T cell proliferation
|
J:48236
|
MybM303V/MybM303V
(involves: 129S1/SvlmJ * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:96507
|
Mybl1repro9/Mybl1repro9
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal double-strand DNA break repair
|
J:175539
|
abnormal male germ cell apoptosis
|
J:175539
|
abnormal synaptonemal complex
|
J:175539
|
arrest of male meiosis
|
J:175539
|
azoospermia
|
J:175539
|
Mybl1repro9/Mybl1tm1Epr
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal synaptonemal complex
|
J:175539
|
arrest of male meiosis
|
J:175539
|
azoospermia
|
J:175539
|
Mybl1tm1Epr/Mybl1tm1Epr
(Not Specified)
|
abnormal spermatocyte morphology
|
J:39632
|
abnormal synaptonemal complex
|
J:175539
|
arrest of male meiosis
|
J:39632,
J:175539
|
azoospermia
|
J:39632,
J:175539
|
decreased male germ cell number
|
J:39632
|
increased male germ cell apoptosis
|
J:39632
|
Mybl2tm1.1Epr/Mybl2tm1.1Epr Tg(Mx1-cre)1Cgn/0
(involves: 129X1/SvJ * C57BL/6 * CBA * FVB/N)
|
abnormal cell cycle
|
J:206816
|
decreased hematopoietic stem cell proliferation
|
J:206816
|
Mybl2tm1.1Jof/Mybl2tm1.1Jof Tg(Mx1-cre)1Cgn/0
(involves: 129S2/SvPas * C57BL/6 * CBA * SJL)
|
abnormal cell cycle
|
J:103413
|
Mybpc3DBA/2J/Mybpc3DBA/2J Myh7DBA/2J/Myh7DBA/2J
(DBA/2J)
|
cardiac interstitial fibrosis
|
J:225492
|
Mybpc3tm1.1Jse/Mybpc3tm1.1Jse
(Not Specified)
|
cardiac interstitial fibrosis
|
J:58295
|
Mybpc3tm1Jse/Mybpc3tm1Jse
(Not Specified)
|
cardiac interstitial fibrosis
|
J:58295
|
Mybpc3tm1Lcrr/Mybpc3tm1Lcrr
(involves: 129S4/SvJae * Black Swiss)
|
cardiac interstitial fibrosis
|
J:101903
|
Mybpc3tm1Rmos/Mybpc3tm1Rmos
(either: (involves: 129) or (involves: 129 * C57BL/6))
|
cardiac interstitial fibrosis
|
J:95725
|
Mybpc3tm2.1Lcrr/Mybpc3tm2.1Lcrr
(involves: 129S2/SvPasCrl * Black Swiss * C57BL/6 * CD-1 * DBA/2)
|
cardiac interstitial fibrosis
|
J:164934
|
Mybpc3tm2.1Rmos/Mybpc3tm2.1Rmos A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129 * C57BL/6 * FVB/N)
|
cardiac interstitial fibrosis
|
J:202199
|
Myctm1.1Itl/Myctm1.1Itl
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
abnormal enterocyte proliferation
|
J:188927
|
abnormal intestinal goblet cell morphology
|
J:188927
|
Myctm1Atp/Myc+
(involves: 129P2/OlaHsd * FVB/N)
|
decreased fibroblast proliferation
|
J:73369
|
decreased T cell proliferation
|
J:73369
|
Myctm1Atp/Myc+
(B6.129P2-Myctm1Atp)
|
decreased T cell proliferation
|
J:132730
|
Myctm1Atp/Myctm1Atp
(involves: 129P2/OlaHsd * FVB/N)
|
absent fibroblast proliferation
|
J:73369
|
Myctm1Atp/Myctm2.1Atp
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL)
|
decreased T cell proliferation
|
J:73369
|
Myctm1Jlc/Myctm1Jlc
(involves: 129S7/SvEvBrd)
|
decreased cell proliferation
|
J:79427
|
Myctm1Lbox/Myctm1Lbox
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
increased B cell apoptosis
|
J:97900
|
increased B cell proliferation
|
J:97900
|
Myctm2.1Atp/Myc+
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
decreased T cell proliferation
|
J:73369
|
Myctm2.1Atp/Myctm2.1Atp Tg(Mx1-cre)1Cgn/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N * SJL)
|
absent fibroblast proliferation
|
J:73369
|
Myctm2Fwa/Myctm2Fwa Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * 129S6/SvEvTac)
|
decreased B cell proliferation
|
J:67222
|
Myctm4.1Fwa/Myctm4.1Fwa
(involves: 129S6/SvEvTac)
|
induced chromosome breakage
|
J:150339
|
Myctm37Mnz/Myc+
(involves: C57BL/6)
|
induced chromosome breakage
|
J:145691
|
Myctm39Mnz/Myc+
(involves: C57BL/6)
|
spontaneous chromosome breakage
|
J:145691
|
Mycbp2mgln/Mycbp2mgln Tg(Isl1-EGFP*)1Slp/0
(B6.Cg-Mycbp2mgln Tg(Isl1-EGFP*)1Slp)
|
abnormal axon extension
|
J:132726
|
Mycbp2tm1.1Adia/Mycbp2tm1.1Adia
(involves: C57BL/6 * FVB/N)
|
abnormal axon guidance
|
J:125702
|
Mycntm1Fwa/Mycntm1Fwa
(involves: 129S/SvEv)
|
increased hepatocyte apoptosis
|
J:46520
|
Mycntm1Jrt/Mycntm1Par
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal fetal cardiomyocyte proliferation
|
J:15281
|
Mycntm1Psk/Mycntm1Psk Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:79489
|
abnormal neuronal precursor proliferation
|
J:79489
|
premature neuronal precursor differentiation
|
J:79489
|
Myd88tm1Aki/Myd88tm1Aki
(Not Specified)
|
decreased B cell proliferation
|
J:96773
|
Myd88tm1Aki/Myd88tm1Aki
(B6.129P2-Myd88tm1Aki)
|
abnormal dendritic cell differentiation
|
J:139001
|
abnormal neuron differentiation
|
J:129957
|
increased apoptosis
|
J:102879
|
Myd88tm1Aki/Myd88tm1Aki Tnfaip3tm1.1Gvl/Tnfaip3tm1.1Gvl Tg(Vil1-cre)997Gum/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
increased enterocyte apoptosis
|
J:163410
|
Myd88tm1Defr/Myd88tm1Defr Tg(Itgax-cre)1-1Reiz/0
(B6.Cg-Myd88tm1Defr Tg(Itgax-cre)1-1Reiz)
|
abnormal dendritic cell differentiation
|
J:139001
|
Myf5tm1Pas/Myf5tm1Pas
(involves: 129 * C57BL/6 * DBA/2)
|
abnormal muscle precursor cell migration
|
J:92799
|
Myf5tm1Tajb/Myf5tm1Tajb
(involves: 129/Sv * C57BL/6 * DBA/2)
|
abnormal muscle precursor cell migration
|
J:92799
|
Myf5tm2Tajb/Myf5tm2Tajb
(involves: 129/Sv * C57BL/6 * DBA/2)
|
abnormal muscle precursor cell migration
|
J:92799
|
Myf5tm2Tajb/Myf5tm2Tajb
(involves: 129S2/SvPas)
|
abnormal skeletal muscle satellite cell proliferation
|
J:128921
|
Myf5tm3(cre)Sor/Myf5+ Sik1tm1.1Berd/Sik1tm1.1Berd
(involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J * SJL)
|
increased skeletal muscle cell glucose uptake
|
J:236223
|
Myh3tm1.2Sajm/Myh3tm1.1Sajm Pax7tm1(cre)Mrc/Pax7+
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J)
|
cellular phenotype
|
J:287755
|
Myh3tm1.2Sajm/Myh3tm1.2Sajm
(involves: 129S1/Sv * 129S4/SvJaeSor * C57BL/6J)
|
increased myoblast apoptosis
|
J:287755
|
Myh6tm1Jse/Myh6+
(involves: 129X1/SvJ)
|
cardiac interstitial fibrosis
|
J:32960
|
Myh6tm1Jse/Myh6+ Tg(Myh6-TNNI3*G203S)1Chs/0
(involves: 129X1/SvJ * C57BL/6)
|
cardiac interstitial fibrosis
|
J:153302
|
Myh6tm2Jse/Myh6+
(involves: 129)
|
cardiac interstitial fibrosis
|
J:247162
|
Myh6tm2Jse/Myh6tm2Jse
(involves: 129)
|
increased cardiomyocyte apoptosis
|
J:247162
|
Myh6tm3.1Jse/Myh6+
(involves: 129)
|
cardiac interstitial fibrosis
|
J:247162
|
Myh6tm3.1Jse/Myh6tm3.1Jse
(involves: 129)
|
increased cardiomyocyte apoptosis
|
J:247162
|
Myh9tm1.1Dash/Myh9+
(involves: 129S2/SvPas * C57BL/6 * C57BL/6J * CBA)
|
abnormal megakaryocyte differentiation
|
J:204923
|
Myh9tm2(GFP/MYH10)Rsad/Myh9tm2(GFP/MYH10)Rsad
(involves: 129S4/SvJae * C57BL/6)
|
abnormal actin cytoskeleton morphology
|
J:163702
|
abnormal cell adhesion
|
J:163702
|
abnormal cell migration
|
J:163702
|
Myh9tm3(GFP/MYH9/MYH10)Rsad/Myh9tm3(GFP/MYH9/MYH10)Rsad
(involves: 129S4/SvJae * C57BL/6)
|
abnormal actin cytoskeleton morphology
|
J:163702
|
abnormal cell adhesion
|
J:163702
|
abnormal cell migration
|
J:163702
|
Myh9tm4(GFP/MYH10/MYH9)Rsad/Myh9tm4(GFP/MYH10/MYH9)Rsad
(involves: 129S4/SvJae * C57BL/6)
|
abnormal actin cytoskeleton morphology
|
J:163702
|
abnormal cell adhesion
|
J:163702
|
abnormal cell migration
|
J:163702
|
Myh9tm5Rsad/Myh9tm5Rsad
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal leukocyte migration
|
J:164684
|
Myh9tm5Rsad/Myh9tm5Rsad Tg(Lck-cre)#Nik/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA/2)
|
abnormal leukocyte adhesion
|
J:164684
|
abnormal leukocyte migration
|
J:164684
|
Myh10tm2Rsad/Myh10tm2Rsad
(involves: 129S4/SvJae)
|
decreased fetal cardiomyocyte proliferation
|
J:92230
|
increased cardiomyocyte apoptosis
|
J:248868
|
Myh10tm2Rsad/Myh10tm2Rsad Myh14tm1Rsad/Myh14tm1Rsad
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6)
|
abnormal centrosome morphology
|
J:168304
|
abnormal microtubule cytoskeleton morphology
|
J:168304
|
abnormal mitosis
|
J:168304
|
abnormal mitotic spindle morphology
|
J:168304
|
Myh10tm3.1Rsad/Myh10tm3.1Rsad
(involves: 129S6/SvEvTac * BALB/c * C57BL/6)
|
decreased apoptosis
|
J:245570
|
Myh10tm3Rsad/Myh10tm3Rsad
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased neuronal migration
|
J:92081
|
Myh10tm4Rsad/Myh10tm4Rsad
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal neuronal migration
|
J:112536
|
Myh10tm6(Myh9/GFP)Rsad/Myh10tm6(Myh9/GFP)Rsad
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal neuronal migration
|
J:124610
|
cardiac interstitial fibrosis
|
J:124610
|
Myh10tm7Rsad/Myh10tm7Rsad Tg(Myh6-cre)2182Mds/0
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N)
|
cardiac interstitial fibrosis
|
J:170148
|
increased cardiomyocyte apoptosis
|
J:170148
|
Myh11tm1.1Dmmz/Myh11tm1.1Dmmz
(involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6)
|
abnormal cell adhesion
|
J:212664
|
increased vascular smooth muscle cell proliferation
|
J:212664
|
Myh11tm1Bdr/Myh11tm1Bdr
(Not Specified)
|
abnormal vascular regression
|
J:82859
|
Myl1tm1(cre)Sjb/0 Ndufab1tm1Xiwa/Ndufab1tm1Xiwa
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
disorganized mitochondrial cristae
|
J:293657
|
Myl1tm1(cre)Sjb/Myl1+ Tfamtm1Lrsn/Tfamtm1Lrsn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal respiratory electron transport chain
|
J:81561
|
Myl2tm1(cre)Krc/Myl2+ Nkx2-5tm1Krc/Nkx2-5tm1Krc
(either: (involves: 129/Sv * Black Swiss) or (involves: 129/Sv * C57BL/6))
|
cardiac interstitial fibrosis
|
J:89404
|
Myl2tm1(cre)Krc/Myl2+ Ptk2tm1.1Guan/Ptk2tm1.1Guan
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
cardiac interstitial fibrosis
|
J:105371
|
Myl2tm1(cre)Krc/Myl2+ Srsf2tm1Xdfu/Srsf2tm1Xdfu
(involves: 129S4/SvJae)
|
cardiac interstitial fibrosis
|
J:88432
|
Mylk3tm1Jtst/Mylk3tm1Jtst
(involves: 129S/SvEv * C57BL/6)
|
cardiac interstitial fibrosis
|
J:167590
|
Mymktm1e(KOMP)Wtsi/Mymktm1e(KOMP)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
abnormal myoblast differentiation
|
J:200444
|
abnormal myoblast fusion
|
J:200444
|
increased apoptosis
|
J:200444
|
Mymxem1Shcs/Mymxem1Shcs
(involves: C57BL/6J)
|
abnormal myoblast fusion
|
J:241564
|
Myo1ctm1.1Biat/Myo1ctm1.1Biat
(B6N.129S2-Myo1ctm1.1Biat)
|
cellular phenotype
|
J:200573
|
Myo1ftm1.1Flv/Myo1ftm1.1Flv
(involves: 129S6/SvEvTac)
|
abnormal cell adhesion
|
J:113020
|
impaired neutrophil chemotaxis
|
J:113020
|
Myo1gtm1.2Mfk/Myo1gtm1.2Mfk
(Not Specified)
|
impaired B cell migration
|
J:209304
|
Myo6chl/Myo6chl
(involves: C57BL/6JAnu)
|
abnormal outer hair cell kinocilium morphology
|
J:196601
|
Myo6ksv/Myo6ksv
(B6JJcl.Cg-Myo6ksv)
|
abnormal kinocilium morphology
|
J:245687
|
Myo7aewaso/Myo7aewaso
(involves: C57BL/6J)
|
abnormal cochlear basement membrane morphology
|
J:195666
|
Myo9aem1Atuf/Myo9a+
(C57BL/6J-Myo9aem1Atuf)
|
abnormal podocyte adhesion
|
J:302901
|
decreased podocyte motility
|
J:302901
|
Myo9btm1.2Bah/Myo9btm1.2Bah
(B6.Cg-Myo9btm1.2Bah)
|
impaired macrophage chemotaxis
|
J:162326
|
Myocdtm1.1Msp/mgb
(involves: 129/Sv * FVB/N)
|
patent ductus arteriosus
|
J:283803
|
Myocdtm1Msp/Myocdtm1Msp
(involves: 129)
|
increased cardiomyocyte apoptosis
|
J:154666
|
Myocdtm1Msp/Myocdtm1Msp A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129/Sv * C57BL/6J * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:154666
|
Myocdtm1Msp/Myocdtm1Msp H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129/Sv * C57BL/6 * CBA)
|
patent ductus arteriosus
|
J:131288
|
Myocdtm1Msp/Myocdtm1Msp Tg(Pax3-cre)1Joe/0
(involves: 129/Sv * C57BL/6 * SJL)
|
patent ductus arteriosus
|
J:131288
|
Myogtm1Whk/Myogtm1Whk
(involves: 129S7/SvEvBrd)
|
abnormal myoblast differentiation
|
J:22984
|
Myoz2tm1Eno/Myoz2+ Tg(Myh6-MYOZ2*I246M)#Ajm/0
(involves: 129/Sv * FVB/N)
|
cardiac interstitial fibrosis
|
J:210073
|
Mypntm1.1Epu/Mypn+
(either: (involves: 129S6/SvEv) or (involves: 129S6/SvEv * C57BL/6NCrl))
|
cardiac interstitial fibrosis
|
J:243710
|
Myt1lem1Jdd/Myt1l+
(C57BL/6-Myt1lem1Jdd/J)
|
decreased neuronal precursor proliferation
|
J:321206
|
n-TRtct5m1J/n-TRtct5m1J
(C57BL/6J)
|
abnormal ribosomal stalling
|
J:211326
|
n-TUtca2tm2Mym/n-TUtca2tm2.1Mym Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
increased apoptosis
|
J:130723
|
increased cellular sensitivity to oxidative stress
|
J:130723
|
Naa10tm1Jprk/Naa10tm1Jprk
(B6.129P2-Naa10tm1Jprk)
|
abnormal osteoblast physiology
|
J:276208
|
enhanced osteoblast differentiation
|
J:276208
|
Naa40tm1Qwzh/Naa40tm1Qwzh Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(B6.Cg-Speer6-ps1Tg(Alb-cre)21Mgn Naa40tm1Qwzh)
|
increased fatty acid oxidation
|
J:183119
|
Nab1tm1Jmi/Nab1tm1Jmi Nab2tm1Jmi/Nab2tm1Jmi
(involves: 129X1/SvJ)
|
increased keratinocyte proliferation
|
J:99824
|
increased Schwann cell proliferation
|
J:99824
|
Nabp1tm1.1Kkha/Nabp1tm1.1Kkha
(B6.Cg-Nabp1tm1.1Kkha)
|
cellular phenotype
|
J:220670
|
Nabp1tm1Kkha/Nabp1tm1Kkha
(involves: C57BL/6)
|
cellular phenotype
|
J:220670
|
Nabp2tm1.1Kkha/Nabp2tm1.1Kkha Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal male germ cell apoptosis
|
J:195140
|
abnormal male germ cell morphology
|
J:195140
|
chromosomal instability
|
J:195140
|
increased cellular sensitivity to ionizing radiation
|
J:195140
|
increased thymocyte apoptosis
|
J:195140
|
oligozoospermia
|
J:195140
|
Nabp2tm1.1Schg/Nabp2tm1.1Schg
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal telomere morphology
|
J:228558
|
chromosomal instability
|
J:228558
|
Nabp2tm1.2Kkha/Nabp2tm1.2Kkha
(involves: BALB/cJ * C57BL/6J)
|
cellular phenotype
|
J:195140
|
Nabp2tm1.2Nfel/Nabp2tm1.2Nfel
(involves: C57BL/6 * FVB/N * SJL)
|
chromosomal instability
|
J:190019
|
increased embryonic tissue cell apoptosis
|
J:190019
|
Nabp2tm1Schg/Nabp2tm1Schg
(involves: 129S7/SvEvBrd * C57BL/6)
|
chromosomal instability
|
J:228558
|
Nacatm1Dsr/Nacatm1Dsr
(129S6/SvEvTac-Nacatm1Dsr)
|
abnormal fetal cardiomyocyte proliferation
|
J:167169
|
Nadk2tm1a(EUCOMM)Wtsi/Nadk2tm1a(EUCOMM)Wtsi
(involves: C57BL/6N * C57BL/6NTac)
|
decreased fatty acid oxidation
|
J:255700
|
oxidative stress
|
J:255700
|
Nae1tm1c(EUCOMM)Wtsi/Nae1tm1c(EUCOMM)Wtsi Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6J * C57BL/6N * FVB/N * SJL)
|
decreased fetal cardiomyocyte proliferation
|
J:261328
|
Naglutm1Efn/Naglutm1Efn
(involves: 129S/SvEv * C57BL/6J)
|
abnormal lysosome morphology
|
J:129390
|
Nagpatm1Skor/Nagpatm1Skor
(involves: 129S5/SvEvBrd * C57BL/6)
|
increased lysosomal enzyme secretion
|
J:164482
|
Naip1tm1Aem/Naip1tm1Aem
(129X1/SvJ-Naip1tm1Aem)
|
increased susceptibility to neuronal excitotoxicity
|
J:60925
|
Naip5tm1Vnce/Naip5tm1Vnce
(C57BL/6-Naip5tm1Vnce)
|
decreased cell death
|
J:141008
|
Naipctm1.1Kmma/Naipctm1.1Kmma
(involves: BALB/cJ * C57BL/6)
|
decreased enterocyte apoptosis
|
J:222114
|
Nampttm1Oleo/Nampttm1Oleo Tg(Rho-icre)1Ck/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal mitochondrial crista morphology
|
J:265592
|
abnormal mitochondrial morphology
|
J:265592
|
NanogGt(D042B07)Wrst/NanogGt(D042B07)Wrst
(involves: 129S2/SvPas * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:163559
|
NanogGt(D047A12)Wrst/NanogGt(D047A12)Wrst
(involves: 129S2/SvPas * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:163559
|
Nanos2tm1Ysa/Nanos2tm1Ysa
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
azoospermia
|
J:86522
|
Nanos2tm1Ysa/Nanos2tm1Ysa
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal male germ cell morphology
|
J:132711
|
azoospermia
|
J:132711
|
Nanos2tm1Ysa/Nanos2tm1Ysa Stra8tm1Ysa/Stra8+
(involves: 129 * C57BL/6NCrlj * CBA/JNCrlj * Jcl:MCH(ICR))
|
abnormal male meiosis
|
J:205334
|
Nanos2tm1Ysa/Nanos2tm1Ysa Stra8tm1Ysa/Stra8tm1Ysa
(involves: 129 * C57BL/6NCrlj * CBA/JNCrlj * Jcl:MCH(ICR))
|
abnormal male meiosis
|
J:205334
|
Nanos2tm1Ysa/Nanos2tm3Ysa
(involves: 129 * C57BL/6 * CBA * ICR)
|
decreased male germ cell number
|
J:119032
|
Nanos2tm3Ysa/Nanos2tm3Ysa
(involves: C57BL/6 * CBA * ICR)
|
decreased male germ cell number
|
J:119032
|
Nanos3tm1Ysa/Nanos3tm1Ysa
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
absent germ cells
|
J:86522
|
azoospermia
|
J:86522
|
decreased primordial germ cell number
|
J:86522
|
Nanos3tm2(cre)Ysa/Nanos3+ Tg(CAG-cat,-Nanos2)1Ysa/0
(Not Specified)
|
abnormal female germ cell morphology
|
J:132711
|
abnormal female meiosis
|
J:132711
|
Nap1l1em1Jwji/Nap1l1em1Jwji
(Not Specified)
|
decreased neuronal precursor proliferation
|
J:263406
|
Nbeal2tm1a(EUCOMM)Wtsi/Nbeal2tm1a(EUCOMM)Wtsi
(C57BL/6N-Nbeal2tm1a(EUCOMM)Wtsi/Wtsi)
|
abnormal megakaryocyte differentiation
|
J:220801
|
Nbeal2tm1Lex/Nbeal2tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
impaired myofibroblast differentiation
|
J:201413
|
Nbnem3Jpt/Nbnem3Jpt
(Not Specified)
|
increased cellular sensitivity to ionizing radiation
|
J:251434
|
Nbnem4Jpt/Nbnem4Jpt
(Not Specified)
|
increased cellular sensitivity to ionizing radiation
|
J:251434
|
Nbntm1Jpt/Nbntm1Jpt
(involves: 129S7/SvEvBrd)
|
abnormal cell cycle checkpoint function
|
J:75956
|
cellular phenotype
|
J:144172
|
chromosome breakage
|
J:75956
|
increased cellular sensitivity to gamma-irradiation
|
J:75956
|
Nbntm1Md/Nbntm1Zqw Tg(Mx1-cre)1Cgn/0
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA)
|
chromosome breakage
|
J:93598
|
Nbntm1Nus/Nbntm1Nus
(involves: 129 * C57BL/6)
|
decreased inner cell mass proliferation
|
J:68993
|
Nbntm1Nus/Nbntm2Nus Tg(CD19-cre/ERT2)1Cgn/0
(Not Specified)
|
decreased B cell proliferation
|
J:96102
|
Nbntm1Nus/Nbntm2Nus Tg(Spo11-cre)D5Mpel/0
(involves: BALB/c * C57BL/6)
|
decreased oocyte number
|
J:166888
|
Nbntm1Xu/Nbntm1Xu
(Not Specified)
|
abnormal cell cycle
|
J:75272
|
absent oocytes
|
J:75272
|
decreased fibroblast proliferation
|
J:75272
|
increased cellular sensitivity to gamma-irradiation
|
J:75272
|
Nbntm1Zqw/Nbn+
(involves: 129S2/SvPas * C57BL/6)
|
chromosomal instability
|
J:86563
|
Nbntm1Zqw/Nbntm1Zqw
(involves: 129S2/SvPas * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:86563
|
absent inner cell mass proliferation
|
J:86563
|
increased apoptosis
|
J:86563
|
Nbntm2.1Jpt/Nbn+ Rad50tm2Jpt/Rad50tm2Jpt
(involves: 129S7/SvEvBrd * 129/Sv)
|
decreased apoptosis
|
J:129762
|
Nbntm2.1Jpt/Nbntm2.1Jpt
(involves: 129)
|
decreased cellular sensitivity to ionizing radiation
|
J:129762
|
Nbntm2.1Jpt/Nbntm2.1Jpt Rad50tm2Jpt/Rad50tm2Jpt
(involves: 129S7/SvEvBrd * 129/Sv)
|
decreased apoptosis
|
J:129762
|
Nbntm2Zqw/Nbntm2.1Zqw Tg(Nes-cre)1Wme/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal neuron differentiation
|
J:98316
|
Nbntm2Zqw/Nbntm2Zqw Tg(Nes-cre)1Wme/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal neuron differentiation
|
J:98316
|
Nbntm3Jpt/Nbntm3Jpt
(involves: 129)
|
decreased cellular sensitivity to ionizing radiation
|
J:144172
|
Nbr1tm1Whca/Nbr1tm1Whca
(B6.129P2-Nbr1tm1Whca)
|
abnormal osteoblast differentiation
|
J:162412
|
Ncaldtm1.1(KOMP)Vlcg/Ncald+
(B6N(Cg)-Ncaldtm1.1(KOMP)Vlcg/J)
|
abnormal axon extension
|
J:273172
|
Ncaldtm1.1(KOMP)Vlcg/Ncaldtm1.1(KOMP)Vlcg
(B6N(Cg)-Ncaldtm1.1(KOMP)Vlcg/J)
|
abnormal axon extension
|
J:273172
|
abnormal neuronal migration
|
J:273172
|
impaired neuron differentiation
|
J:273172
|
Ncam1tm1Cgn/Ncam1tm1Cgn
(B6.129P2-Ncam1tm1Cgn)
|
abnormal neuron differentiation
|
J:126687
|
Ncam2tm1.1Bdrt/Ncam2tm1.1Bdrt
(involves: 129S4/SvJae * C57BL/6)
|
abnormal neuron proliferation
|
J:233502
|
Ncapg2tm1Jdc/Ncapg2tm1Jdc
(involves: 129S1/Sv * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:87685
|
absent inner cell mass proliferation
|
J:87685
|
Ncaph2nes/Ncaph2nes
(C57BL/6-Ncaph2nes)
|
abnormal mitosis
|
J:242515
|
Ncaph2tm1.1Hiran/Ncaph2tm1.2Hiran Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal cell nucleus morphology
|
J:222181
|
abnormal mitosis
|
J:222181
|
abnormal nucleolus morphology
|
J:222181
|
Ncaphtm1.1Hiran/Ncaphtm1.2Hiran Ncaph2tm1.1Hiran/Ncaph2tm1.2Hiran Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal cell nucleus morphology
|
J:222181
|
abnormal mitosis
|
J:222181
|
Ncaphtm1.1Hiran/Ncaphtm1.2Hiran Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal mitosis
|
J:222181
|
Nceh1tm1Ishi/Nceh1tm1Ishi
(B6.129S7-Nceh1tm1Ishi)
|
decreased cholesterol efflux
|
J:152385
|
Ncf1m1J/Ncf1m1J
(involves: C57BL/6)
|
oxidative stress
|
J:207291
|
Ncf1tm1Shl/Ncf1tm1Shl
(involves: 129S2/SvPas)
|
abnormal intestinal goblet cell morphology
|
J:206181
|
Ncf2tm1b(EUCOMM)Wtsi/Ncf2+
(NZM2328.B6(Cg)-Ncf2tm1b(EUCOMM)Wtsi)
|
abnormal redox activity
|
J:260777
|
Ncf2tm1b(EUCOMM)Wtsi/Ncf2tm1b(EUCOMM)Wtsi
(NZM2328.B6(Cg)-Ncf2tm1b(EUCOMM)Wtsi)
|
abnormal redox activity
|
J:260777
|
Nck1tm1Paw/Nck1tm1Paw Nck2tm1Paw/Nck2tm1Paw
(involves: 129/Ola * ICR)
|
abnormal cell physiology
|
J:83956
|
Nck1tm1Paw/Nck1tm1Paw Nck2tm1Paw/Nck2tm3Paw Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
abnormal axon guidance
|
J:129166
|
Nckap1Gt(RRQ139)Byg/Nckap1Gt(RRQ139)Byg
(involves: 129P2/OlaHsd * C3H)
|
abnormal anterior visceral endoderm cell migration
|
J:166095
|
abnormal cell migration
|
J:173526
|
increased apoptosis
|
J:173526
|
Nckap1khlo/Nckap1khlo
(C3Fe.B6-Nckap1khlo)
|
abnormal anterior visceral endoderm cell migration
|
J:119028
|
Nckap1lm1Iri/Nckap1lm1Iri
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:141377
|
impaired macrophage phagocytosis
|
J:141377
|
impaired neutrophil chemotaxis
|
J:141377
|
impaired neutrophil phagocytosis
|
J:141377
|
Nckipsdtm1.2Toft/Nckipsdtm1.2Toft
(involves: 129S2/SvPas * C57BL/6 * FVB/N)
|
abnormal cell adhesion
|
J:158332
|
abnormal cell migration
|
J:158332
|
abnormal cell morphology
|
J:158332
|
Nckipsdtm1Wkso/Nckipsdtm1Wkso
(B6.Cg-Nckipsdtm1Wkso)
|
abnormal actin cytoskeleton morphology
|
J:148711
|
Nclem1Mfz/Ncl+
(either: (involves: BALB/cAnNHsd * C57BL/6JOlaHsd * C57BL/6NHsd) or (involves: BALB/cAnNHsd * C57BL/6NHsd * ICR))
|
abnormal axon extension
|
J:312459
|
Ncoa2tm1.2Ipc/Ncoa2tm1.2Ipc
(involves: 129S2/SvPas * C57BL/6)
|
abnormal spermatid morphology
|
J:78075
|
detached acrosome
|
J:78075
|
teratozoospermia
|
J:78075
|
Ncoa3tm1.1Bwo/Ncoa3tm1.1Bwo
(involves: 129S/SvEv * C57BL/6J)
|
abnormal cell differentiation
|
J:161276
|
Ncoa3tm1Jxu/Ncoa3tm1Jxu
(involves: 129S6/SvEvTac)
|
decreased fibroblast cell migration
|
J:88789
|
Ncoa3tm1Jxu/Ncoa3tm1Jxu
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal cell differentiation
|
J:117159
|
decreased splenocyte apoptosis
|
J:109522
|
increased B cell proliferation
|
J:109522
|
increased mitochondrial size
|
J:144060
|
increased T cell proliferation
|
J:109522
|
Ncoa3tm1Jxu/Ncoa3tm1Jxu Tg(MMTV-vHaras)SH1Led/0
(involves: 129S6/SvEvTac * C57BL/6J * CD-1)
|
abnormal cell migration
|
J:88789
|
decreased mammary gland epithelial cell proliferation
|
J:88789
|
Ncoa3tm1Rsd/Ncoa3tm1Rsd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:66454
|
decreased cell proliferation
|
J:66454
|
Ncoa4tm1Msnt/Ncoa4tm1Msnt
(B6.Cg-Ncoa4tm1Msnt)
|
abnormal DNA replication
|
J:215322
|
decreased fibroblast proliferation
|
J:215322
|
early cellular replicative senescence
|
J:215322
|
Ncoa5tm1Hxia/Ncoa5+
(involves: 129 * C57BL/6)
|
abnormal sperm head morphology
|
J:284227
|
abnormal sperm midpiece morphology
|
J:284227
|
abnormal sperm mitochondrial morphology
|
J:284227
|
asthenozoospermia
|
J:284227
|
decreased sperm progressive motility
|
J:284227
|
increased hepatocyte apoptosis
|
J:207622
|
increased hepatocyte proliferation
|
J:207622
|
teratozoospermia
|
J:284227
|
Ncoa6tm1.1Jkr/Ncoa6tm1.1Jkr
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
abnormal fetal cardiomyocyte proliferation
|
J:81217
|
increased hepatocyte apoptosis
|
J:81217
|
Ncoa6tm1Hhs/Ncoa6tm1Hhs
(either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6))
|
decreased fibroblast proliferation
|
J:91083
|
increased fibroblast apoptosis
|
J:91083
|
Ncoa6tm1Hhs/Ncoa6tm1Hhs
(involves: 129S6/SvEvTac)
|
abnormal cell physiology
|
J:116064
|
Ncoa6tm1Jkr/Ncoa6tm1Jkr Tg(Myh6-cre)2182Mds/0
(involves: 129P2/OlaHsd * FVB/N)
|
decreased mitochondrial number
|
J:269856
|
Ncoa6tm1Jxu/Ncoa6tm1Jxu
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:80175
|
Ncoa7em1Pelo/Ncoa7em1Pelo
(C57BL/6-Ncoa7em1Pelo)
|
abnormal lysosome morphology
|
J:305611
|
abnormal lysosome physiology
|
J:305611
|
Ncor1tm1.1Ics/Ncor1tm1.1Ics Tg(ACTA1-cre)79Jme/0
(involves: 129 * C57BL/6 * C57BL/6J * SJL)
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:178827
|
increased skeletal muscle fiber mitochondrial size
|
J:178827
|
Ncor1tm1Rsd/Ncor1+ Ncor2tm1Rsd/Ncor2+
(involves: 129/Sv * 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:127720
|
Ncor2Gt(RRM275)Byg/Ncor2+
(B6.129P2-Ncor2Gt(RRM275)Byg)
|
abnormal cell differentiation
|
J:164558
|
Ncor2tm1Rev/Ncor2tm1Rev
(involves: 129/Sv * C57BL/6)
|
abnormal cell differentiation
|
J:142665
|
Ncor2tm1Rsd/Ncor2tm1Rsd
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuronal precursor proliferation
|
J:127720
|
Ncstntm1.1Sud/Ncstntm1.1Sud Tg(Camk2a-cre)1Shn/0
(B6.Cg-Ncstntm1.1Sud Tg(Camk2a-cre)1Shn)
|
increased neuron apoptosis
|
J:149506
|
Ncstntm1Pcw/Ncstntm1Pcw
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:83376
|
Ncstntm1Rroz/Ncstntm1Rroz
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
increased apoptosis
|
J:108976
|
increased embryonic neuroepithelium apoptosis
|
J:108976
|
Ndc1sks/Ndc1sks
(involves: A/J)
|
abnormal male meiosis
|
J:9569
|
arrest of male meiosis
|
J:9569
|
Ndc80tm1Tski/Ndc80tm1Tski Tg(Zp3-cre)3Mrt/0
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj * FVB/N)
|
abnormal meiotic spindle assembly checkpoint
|
J:292307
|
abnormal meiotic spindle morphology
|
J:292307
|
aneuploidy
|
J:292307
|
Nde1tm1Caw/Nde1tm1Caw
(involves: 129S4/SvJae * Black Swiss)
|
abnormal neuron differentiation
|
J:94756
|
decreased neuronal migration
|
J:94756
|
Ndfip1Gt(RRD002)Byg/Ndfip1Gt(RRD002)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased T cell proliferation
|
J:116617
|
Ndfip1Gt(RRD002)Byg/Ndfip1Gt(RRD002)Byg
(involves: 129P2/OlaHsd)
|
increased T cell proliferation
|
J:205692
|
Ndfip1tm1.1Sest/Ndfip1tm1.1Sest
(involves: C57BL/6)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:212711
|
Ndntm1.1Mus/Ndn+
(B6.129S2-Ndntm1.1Mus)
|
maternal imprinting
|
J:119656
|
Ndntm1Ky/Ndn+
(involves: C57BL/6 * CBA * ICR/Slc)
|
maternal imprinting
|
J:100024
|
Ndntm1Stw/Ndn+
(involves: 129S1/Sv * C57BL/6)
|
maternal imprinting
|
J:57890
|
Ndntm1Stw/Ndn+
(involves: 129S1/Sv * FVB)
|
maternal imprinting
|
J:57890
|
Ndntm2Stw/Ndn+
(involves: 129S1/Sv * C57BL/6J)
|
maternal imprinting
|
J:82266
|
Ndntm2Stw/Ndn+
(involves: 129S1/Sv * C57BL/6)
|
maternal imprinting
|
J:57890
|
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+ Rnpc3tm1c(EUCOMM)Wtsi/Rnpc3tm1c(EUCOMM)Wtsi
(involves: 129S/SvEv * C57BL/6 * C57BL/6N)
|
abnormal enterocyte proliferation
|
J:267519
|
abnormal small intestinal crypt cell proliferation
|
J:267519
|
increased small intestinal crypt cell apoptosis
|
J:267519
|
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+ Rragatm2Dmsa/Rragatm2Dmsa
(involves: 129S/SvEv * 129S4/SvJae * C57BL/6)
|
abnormal intestine apoptosis
|
J:213516
|
increased apoptosis
|
J:213516
|
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+ Stag2tm1.1Alos/Y
(involves: 129S6/SvEvTac * C57BL/6NCrl)
|
abnormal enterocyte proliferation
|
J:298088
|
abnormal mitosis
|
J:298088
|
cellular necrosis
|
J:298088
|
decreased fibroblast proliferation
|
J:298088
|
increased fibroblast apoptosis
|
J:298088
|
Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+ Stag2tm1.1Alos/Stag2tm1.1Alos
(involves: 129S6/SvEvTac * C57BL/6NCrl)
|
abnormal enterocyte proliferation
|
J:298088
|
abnormal mitosis
|
J:298088
|
cellular necrosis
|
J:298088
|
decreased fibroblast proliferation
|
J:298088
|
increased fibroblast apoptosis
|
J:298088
|
Ndrg2tm1.1Hori/Ndrg2tm1.1Hori
(B6.129-Ndrg2tm1.1Hori)
|
abnormal microglial cell chemotaxis
|
J:214686
|
decreased neuron apoptosis
|
J:214686
|
Ndrg2tm1Kmori/Ndrg2+
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
increased fibroblast proliferation
|
J:210264
|
Ndrg2tm1Kmori/Ndrg2tm1Kmori
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
increased fibroblast proliferation
|
J:210264
|
Ndrg3em1Qshi/Ndrg3+
(C57BL/6-Ndrg3em1Qshi)
|
abnormal double-strand DNA break repair
|
J:275135
|
abnormal male meiosis
|
J:275135
|
oligozoospermia
|
J:275135
|
Ndst1tm1.1Grob/Ndst1tm1.1Grob Ndst3tm1.1Grob/Ndst3tm1.1Grob
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
decreased fibroblast cell migration
|
J:138557
|
increased hindbrain apoptosis
|
J:138557
|
Ndst1tm1Je/Ndst1tm1Je Tg(Tek-cre)1Ywa/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal leukocyte adhesion
|
J:100456
|
abnormal leukocyte migration
|
J:100456
|
decreased endothelial cell proliferation
|
J:208012
|
impaired leukocyte tethering or rolling
|
J:100456
|
Ndst2tm1Lkj/Ndst2tm1Lkj
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased mast cell degranulation
|
J:57121
|
Ndst2tm1Rls/Ndst2tm1Rls
(Not Specified)
|
decreased mast cell degranulation
|
J:57120
|
Ndst2tm1Rls/Ndst2tm1Rls
(B6.Cg-Ndst2tm1Rls)
|
abnormal mast cell differentiation
|
J:142880
|
Ndst4tm1.1Ntuy/Ndst4tm1.1Ntuy
(involves: 129/Sv * C57BL/6)
|
increased colon goblet cell number
|
J:252046
|
increased enterocyte apoptosis
|
J:252046
|
Ndufa5Gt(RRK279)Byg/Ndufa5Gt(RRK279)Byg Tg(Camk2a-cre)#Szi/0 Tg(Gt(ROSA)26Sor-Ndufa5)#Ctm/0
(involves: 129P2/OlaHsd * C57BL/6J * CBA * SJL)
|
abnormal respiratory electron transport chain
|
J:206222
|
Ndufa13em1Nju/Ndufa13+
(C57BL/6-Ndufa13em1Nju)
|
abnormal mitochondrial physiology
|
J:326065
|
asthenozoospermia
|
J:326065
|
decreased sperm progressive motility
|
J:326065
|
increased male germ cell apoptosis
|
J:326065
|
oligozoospermia
|
J:326065
|
oxidative stress
|
J:326065
|
Ndufa13tm1Xc/Ndufa13tm1Xc
(either: 129X1/SvJ or (involves: 129X1/SvJ * C57BL/6))
|
abnormal mitochondrial crista morphology
|
J:93022
|
abnormal mitochondrial shape
|
J:93022
|
Ndufaf2tm1.1Itl/Ndufaf2tm1.1Itl
(involves: 129S/SvEv * BALB/cJ)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:201547
|
Ndufs4tm1.1Rpa/Ndufs4tm1.1Rpa
(involves: 129/Sv * 129S4/SvJaeSor * C57BL/6)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:134334
|
Ndufs4tm1.1Rpa/Ndufs4tm1.1Rpa
(involves: 129S4/SvJaeSor)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:201547
|
abnormal mitochondrial crista morphology
|
J:161393
|
oxidative stress
|
J:161393
|
Ndufs4tm1Capt/Ndufs4+
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
abnormal respiratory electron transport chain
|
J:192154
|
Ndufs4tm1Rpa/Ndufs4tm1Rpa Tg(Nes-cre)1Kln/0
(involves: 129S4/SvJaeSor * C57BL/6 * SJL)
|
abnormal respiratory electron transport chain
|
J:161393
|
Ndufs6Gt(AR0138)Wtsi/Ndufs6Gt(AR0138)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal mitochondrial morphology
|
J:183619
|
abnormal respiratory electron transport chain
|
J:183619
|
decreased mitochondrial size
|
J:183619
|
Neat1tm1.1Shna/Neat1tm1.1Shna
(involves: 129S4/SvJaeSor * C57BL/6Ncrlj * CBA/JNCrlj)
|
abnormal cell nucleus morphology
|
J:171281
|
Neat1tm1.1Shna/Neat1tm1.1Shna
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
decreased mammary gland epithelial cell proliferation
|
J:228123
|
maternal effect
|
J:228123
|
Necab2tm1a(KOMP)Wtsi/Necab2tm1a(KOMP)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
abnormal spermatid morphology
|
J:213427
|
Nectin2tm1Smu/Nectin2tm1Smu
(involves: 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal sperm head morphology
|
J:85634
|
abnormal sperm midpiece morphology
|
J:85634
|
abnormal sperm mitochondrial sheath morphology
|
J:85634
|
impaired sperm migration in female genital tract
|
J:85634
|
teratozoospermia
|
J:85634
|
Nectin2tm1Vrr/Nectin2tm1Vrr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal acrosome morphology
|
J:61334
|
abnormal sperm flagellum morphology
|
J:61334
|
abnormal sperm head morphology
|
J:61334
|
abnormal sperm midpiece morphology
|
J:61334
|
abnormal sperm nucleus morphology
|
J:61334
|
disorganized sperm mitochondrial sheath
|
J:61334
|
teratozoospermia
|
J:61334
|
Nedd4Gt(XA209)Byg/Nedd4Gt(XA209)Byg
(involves: 129P2/OlaHsd)
|
abnormal neural crest cell physiology
|
J:203994
|
decreased fibroblast proliferation
|
J:207675
|
decreased T cell proliferation
|
J:143560
|
increased cranial neural crest cell apoptosis
|
J:203994
|
increased embryonic neuroepithelium apoptosis
|
J:203994
|
Nedd4Gt(XA209)Byg/Nedd4Gt(XA209)Byg
(B6.129P2-Nedd4Gt(XA209)Byg)
|
abnormal meiosis
|
J:320185
|
Nedd4Gt(XB398)Byg/Nedd4Gt(XB398)Byg
(involves: 129P2/OlaHsd)
|
decreased T cell proliferation
|
J:143560
|
Nedd9tm1Miku/Nedd9tm1Miku
(B6.CBA-Nedd9tm1Miku)
|
abnormal leukocyte migration
|
J:116716
|
Nefhtm1Dwc/Nefhtm1Dwc
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal axon extension
|
J:77654
|
Nefhtm2Dwc/Nefhtm2Dwc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:87156
|
Nefmtm1Milg/Nefmtm1Milg
(involves: 129S/SvEv * C57BL/6)
|
abnormal neuron differentiation
|
J:184861
|
Nefmtm1Mvr/Nefmtm1Mvr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuron differentiation
|
J:87157
|
Nefmtm1Mvr/Nefmtm1Mvr
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:87156
|
Neil1tm1Bjor/Neil1tm1Bjor Tg(HDexon1)61Gpb/0
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal cell physiology
|
J:188338
|
Neil2tm1.1Tkhz/Neil2tm1.1Tkhz
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl)
|
decreased telomere length
|
J:225791
|
oxidative stress
|
J:225791
|
spontaneous chromosome breakage
|
J:225791
|
Neil3tm1Bjor/Neil3tm1Bjor
(involves: 129 * C57BL/6)
|
abnormal DNA repair
|
J:180177
|
abnormal neuron differentiation
|
J:180177
|
abnormal neuronal precursor proliferation
|
J:180177
|
Nek6tm1Dgen/Nek6tm1Dgen
(involves: 129S1/Sv * 129X1/SvJ)
|
cardiac interstitial fibrosis
|
J:215160
|
Nek7tm1Mot/Nek7tm1Mot
(involves: 129S1/Sv * 129X1/SvJ * BALB/c * ICR)
|
abnormal mitosis
|
J:168166
|
aneuploidy
|
J:168166
|
binucleate
|
J:168166
|
chromosomal instability
|
J:168166
|
polyploidy
|
J:168166
|
Nek9em1Nmz/Nek9em1Nmz
(C57BL/6-Nek9em1Nmz)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:314513
|
impaired autophagy
|
J:314513
|
Nell2em1Osb/Nell2em1Osb Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
(involves: C57BL/6NJcl * DBA/2NJcl)
|
impaired sperm migration in female genital tract
|
J:290452
|
Nemp1em1Hmc/Nemp1em1Hmc
(C57BL/6N-Nemp1em1Hmc)
|
abnormal female meiosis
|
J:303621
|
abnormal oocyte morphology
|
J:303621
|
maternal effect
|
J:303621
|
Neprotm1Tets/Neprotm1Tets
(B6JJcl.129-Neprotm1Tets)
|
abnormal cell nucleus morphology
|
J:223645
|
abnormal nucleolus morphology
|
J:223645
|
Nestm1Dopa/Nestm1Dopa
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal neuron differentiation
|
J:168641
|
Nestm1Dopa/Nestm1Dopa Vimtm1Cba/Vimtm1Cba
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6J)
|
abnormal neuron differentiation
|
J:168641
|
Neu1tm1Adz/Neu1tm1Adz
(either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * NMRI))
|
abnormal lysosome morphology
|
J:76937
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:76937
|
Neu4tm1Avps/Neu4tm1Avps
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal lysosome physiology
|
J:135246
|
Neurl1atm1Led/Neurl1atm1Led
(involves: 129S6/SvEvTac)
|
abnormal sperm axoneme morphology
|
J:72105
|
abnormal sperm connecting piece morphology
|
J:72105
|
abnormal sperm fibrous sheath morphology
|
J:72105
|
abnormal spermatid morphology
|
J:72105
|
absent sperm head
|
J:72105
|
asthenozoospermia
|
J:72105
|
biflagellated sperm
|
J:72105
|
teratozoospermia
|
J:72105
|
Neurod1tm1Jle/Neurod1tm1Jle
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal retina apoptosis
|
J:51299
|
Neurod1tm1Jle/Neurod1tm1Jle
(involves: 129S4/SvJaeSor * ICR)
|
increased retina apoptosis
|
J:121047
|
Neurod1tm1Jle/Neurod1tm1Jle Neurod4tm1Kag/Neurod4tm1Kag Neurog2tm1Fgu/Neurog2tm1Fgu
(involves: 129/Sv * C57BL/6 * CBA * ICR)
|
increased retina apoptosis
|
J:121047
|
Neurod1tm1Jle/Neurod1tm1Jle Tg(RIP1-Neurod1)1Jle/0
(involves: 129S4/SvJaeSor * C57BL/6 * CBA)
|
abnormal neuron differentiation
|
J:74715
|
Neurod1tm1Mjts/Neurod1tm1Mjts
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased pancreas apoptosis
|
J:43010
|
Neurog1tm1And/Neurog1tm1And Neurog2tm2Fgu/Neurog2tm2Fgu
(involves: 129/Sv * C57BL/6J * CD-1)
|
abnormal neuron differentiation
|
J:59428
|
Neurog2tm2Fgu/Neurog2tm2Fgu
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:109091
|
Neurog2tm4Fgu/Neurog2tm4Fgu
(involves: MF1)
|
abnormal neuron differentiation
|
J:134976
|
abnormal neuronal migration
|
J:134976
|
abnormal neuronal precursor proliferation
|
J:134976
|
abnormal radial glial cell morphology
|
J:134976
|
Neurog2tm5(Neurog2)Fgu/Neurog2tm5(Neurog2)Fgu
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:109091
|
abnormal neuronal migration
|
J:109091
|
Neurog3tm1Fgu/Neurog3tm3.1Ggr Tg(Vil1-cre)20Syr/0
(involves: 129S2/SvPas * C57BL/6 * CD-1 * DBA/2 * SJL)
|
abnormal intestinal goblet cell morphology
|
J:161480
|
abnormal small intestinal crypt cell proliferation
|
J:161480
|
Neurog3tm3.1Ggr/Neurog3tm3.1Ggr Tg(Vil1-cre)20Syr/0
(involves: 129S2/SvPas * C57BL/6 * CD-1 * DBA/2 * SJL)
|
abnormal intestinal goblet cell morphology
|
J:161480
|
abnormal small intestinal crypt cell proliferation
|
J:161480
|
Nf1Mhdadsk9/Nf1+
(involves: C3HeB/FeJ * C57BL/6)
|
abnormal spermatid morphology
|
J:269534
|
enlarged sperm head
|
J:269534
|
increased round spermatid number
|
J:269534
|
Nf1tm1Fcr/Nf1+ Tg(GFAP-cre)#Gtm/0
(involves: 129S/SvEv * 129S4/SvJae * C57BL/6 * CBA)
|
abnormal neuron proliferation
|
J:176586
|
Nf1tm1Par/Nf1tm1Par Rnf7Gt(XE423)Byg/Rnf7Gt(XE423)Byg
(involves: 129 * C57BL/6)
|
decreased cell proliferation
|
J:178926
|
increased apoptosis
|
J:178926
|
Nf1tm1Par/Nf1tm1Par Tg(Fabp7-cre,-lacZ)3Gtm/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal neuronal precursor proliferation
|
J:139866
|
Nf1tm1Par/Nf1tm1Par Tg(Prrx1-cre)1Cjt/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J)
|
abnormal myoblast differentiation
|
J:173779
|
increased myoblast proliferation
|
J:173779
|
Nf1tm1Tyj/Nf1+
(involves: 129S2/SvPas)
|
increased mast cell degranulation
|
J:142439
|
Nf1tm1Tyj/Nf1tm1Tyj Rasa1tm1Paw/Rasa1tm1Paw
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
increased cranial neural crest cell apoptosis
|
J:29825
|
increased hindbrain apoptosis
|
J:29825
|
Nfat5tm1Rao/Nfat5tm1Rao
(B6.129-Nfat5tm1Rao)
|
increased kidney apoptosis
|
J:88636
|
Nfat5tm1Skc/Nfat5tm1Skc
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:175527
|
Nfat5tm1Snh/Nfat5+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased T cell proliferation
|
J:91482
|
Nfatc1tm1Rao/Nfatc1tm1Rao Cd79atm1(cre)Reth/Cd79a+
(involves: BALB/c)
|
decreased B cell proliferation
|
J:177319
|
increased B cell apoptosis
|
J:177319
|
Nfatc1tm1Rao/Nfatc1tm1Rao Tg(Fcer2a-cre)5Mbu/0
(involves: C57BL/6 * CBA)
|
decreased B cell proliferation
|
J:177319
|
Nfatc1tm3Glm/Nfatc1tm3Glm Sh3bp2tm1Bjro/Sh3bp2tm1Bjro Tg(Mx1-cre)1Cgn/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
abnormal osteoclast differentiation
|
J:144598
|
Nfatc1tm3Glm/Nfatc1tm3Glm Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal osteoclast differentiation
|
J:144598
|
Nfatc2tm1Rao/Nfatc2tm1Rao Nfatc3tm1Grc/Nfatc3tm1Grc Tg(Lck-cre)I57Jxm/0
(involves: ICR)
|
increased T cell apoptosis
|
J:141917
|
Nfatc3tm1Glm/Nfatc3tm1Glm Nfatc4tm1Jmk/Nfatc4tm1Jmk
(involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6)
|
abnormal cellular respiration
|
J:84138
|
abnormal myocardial fiber mitochondrial morphology
|
J:84138
|
Nfatc3tm1Grc/Nfatc3tm1Grc Tg(Lck-cre)I57Jxm/0
(involves: ICR)
|
increased T cell apoptosis
|
J:141917
|
Nfe2l1tm1Ywk/Nfe2l1tm1Ywk
(involves: 129X1/SvJ)
|
oxidative stress
|
J:86725
|
Nfe2l1tm1Ywk/Nfe2l1tm1Ywk Nfe2l2tm1Ywk/Nfe2l2tm1Ywk
(involves: 129X1/SvJ)
|
increased apoptosis
|
J:86725
|
increased cellular sensitivity to oxidative stress
|
J:86725
|
increased fibroblast apoptosis
|
J:86725
|
oxidative stress
|
J:86725
|
Nfe2l2tm1.1Sred/Nfe2l2tm1.1Sred Tg(Scgb1a1-cre)1Grau/0
(involves: C57BL/6 * C57BL/6J)
|
abnormal cell death
|
J:191916
|
Nfe2l2tm1Mym/Nfe2l2tm1Mym
(involves: 129P2/OlaHsd * ICR)
|
increased kidney cell proliferation
|
J:104016
|
increased mesangial cell number
|
J:104016
|
oxidative stress
|
J:104016
|
Nfe2l2tm1Mym/Nfe2l2tm1Mym
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal leukocyte adhesion
|
J:150597
|
increased hepatocyte apoptosis
|
J:136120
|
oxidative stress
|
J:150597
|
Nfe2l2tm1Mym/Nfe2l2tm1Mym n-TUtca2tm2Mym/n-TUtca2tm2.1Mym Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
increased apoptosis
|
J:130723
|
increased cellular sensitivity to hydrogen peroxide
|
J:130723
|
increased cellular sensitivity to oxidative stress
|
J:130723
|
Nfe2l2tm1Mym/Nfe2l2tm1Mym Tg(Alb1-cre)1Dlr/0 n-TUtca2tm2Mym/n-TUtca2tm2.1Mym
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * FVB/N)
|
increased hepatocyte apoptosis
|
J:130723
|
Nfe2l2tm1Ywk/Nfe2l2tm1Ywk
(involves: 129X1/SvJ)
|
decreased hepatocyte proliferation
|
J:130473
|
increased cellular sensitivity to hydrogen peroxide
|
J:91407
|
increased fibroblast apoptosis
|
J:86725
|
increased splenocyte apoptosis
|
J:91407
|
oxidative stress
|
J:130473,
J:91407,
J:86725,
J:122195
|
Nfe2l2tm1Ywk/Nfe2l2tm1Ywk
(B6.129X1-Nfe2l2tm1Ywk/J)
|
oxidative stress
|
J:233699
|
Nfe2l2tm1Ywk/Nfe2l2tm1Ywk
(B6.129X1-Nfe2l2tm1Ywk)
|
abnormal male germ cell morphology
|
J:165602
|
asthenozoospermia
|
J:165602
|
cellular phenotype
|
J:310044
|
increased male germ cell apoptosis
|
J:165602
|
oligozoospermia
|
J:165602
|
oxidative stress
|
J:165602
|
Nfiatm1Rmg/Nfia+
(involves: 129P2/OlaHsd * Black Swiss)
|
maternal effect
|
J:58137
|
Nfiatm1Rmg/Nfiatm1Rmg
(B6.129P2-Nfiatm1Rmg)
|
abnormal axon extension
|
J:81202
|
Nfil3tm1Pbro/Nfil3tm1Pbro
(B6.129S6-Nfil3tm1Pbro)
|
abnormal colon goblet cell morphology
|
J:209365
|
Nfkb1tm1Bal/Nfkb1tm1Bal
(B6;129P-Nfkb1tm1Bal/J)
|
increased apoptosis
|
J:118907
|
Nfkb1tm1Bal/Nfkb1tm1Bal
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:37184,
J:30268
|
Nfkb1tm1Bal/Nfkb1tm1Bal Nfkb2tm1Sbn/Nfkb2tm1Sbn
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
abnormal osteoclast differentiation
|
J:45119
|
Nfkb1tm1Bal/Nfkb1tm1Bal Relatm1Bal/Relatm1Bal
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
abnormal dendritic cell differentiation
|
J:113514
|
Nfkb1tm1Brv/Nfkb1tm1Brv
(involves: 129S1/Sv)
|
decreased T cell proliferation
|
J:46912
|
increased B cell proliferation
|
J:46912
|
Nfkb1tm1Brv/Nfkb1tm1Brv Nfkb2tm1Brv/Nfkb2+
(involves: 129S1/Sv * C57BL/6)
|
abnormal osteoclast differentiation
|
J:44112
|
Nfkb1tm1Brv/Nfkb1tm1Brv Nfkb2tm1Brv/Nfkb2tm1Brv
(involves: 129S1/Sv * C57BL/6)
|
abnormal osteoclast differentiation
|
J:44112
|
Nfkb1tm1Sley/Nfkb1tm1Sley
(involves: 129S4/SvJae * 129S8/SvEv)
|
decreased T cell proliferation
|
J:142340
|
Nfkb2Lym1/Nfkb2Lym1
(involves: BALB/c)
|
abnormal osteoclast differentiation
|
J:154812
|
decreased B cell proliferation
|
J:154812
|
Nfkb2tm1Brv/Nfkb2tm1Brv
(involves: 129S1/Sv * C57BL/6)
|
increased B cell proliferation
|
J:43469
|
increased T cell proliferation
|
J:43469
|
Nfkb2tm1Sbn/Nfkb2tm1Sbn
(involves: 129S4/SvJae)
|
decreased fibroblast cell migration
|
J:159873
|
decreased fibroblast chemotaxis
|
J:159873
|
Nfkb2tm2Brv/Nfkb2tm2Brv
(involves: 129S1/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:76380
|
increased splenocyte apoptosis
|
J:76380
|
Nfkbiatm1.1Pjc/Nfkbiatm1.1Pjc
(involves: C57BL/6)
|
increased T cell apoptosis
|
J:163686
|
increased T cell proliferation
|
J:163686
|
Nfkbiatm1.1Smiy/Nfkbiatm1.1Smiy
(B6.129-Nfkbiatm1.1Smiy)
|
decreased B cell proliferation
|
J:168977
|
increased activation-induced B cell apoptosis
|
J:168977
|
Nfkbiatm1Bal/Nfkbiatm1Bal
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal granulocyte differentiation
|
J:30058
|
Nfkbiatm1Bal/Nfkbiatm1Bal Nfkbietm1Syme/Nfkbietm1Syme
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 * DBA/2)
|
increased B cell apoptosis
|
J:88142
|
increased T cell apoptosis
|
J:88142
|
Nfkbiatm1Fey/Nfkbiatm1Fey
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell differentiation
|
J:110817
|
abnormal cell physiology
|
J:110817
|
decreased T cell proliferation
|
J:110817
|
increased B cell proliferation
|
J:110817
|
Nfkbidm1Btlr/Nfkbidm1Btlr
(involves: C57BL/6J)
|
decreased B cell proliferation
|
J:185495
|
increased B cell apoptosis
|
J:185495
|
Nfkbidtm1Clay/Nfkbidtm1Clay
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased T cell proliferation
|
J:132071
|
Nfkbiztm1.1Muta/Nfkbiztm1.1Muta Tg(KRT5-cre)1Tak/?
(involves: C3H * C57BL/6)
|
increased lacrimal gland apoptosis
|
J:194832
|
Nfkbiztm1Aki/Nfkbiztm1Aki
(involves: 129P2/OlaHsd)
|
increased lacrimal gland apoptosis
|
J:194832
|
Nfyatm1Mait/Nfyatm1.1Mait
(involves: C57BL/6)
|
abnormal cell cycle
|
J:87090
|
decreased fibroblast proliferation
|
J:87090
|
increased fibroblast apoptosis
|
J:87090
|
Ng/Ng
(involves: NMRI)
|
abnormal keratinocyte differentiation
|
J:6028
|
Ngeftm1Meg/Ngeftm1Meg
(involves: 129S4/SvJae)
|
abnormal axon extension
|
J:98309
|
Ngfrtm1Jae/Ngfr+
(B6.129S4-Ngfrtm1Jae)
|
abnormal axon extension
|
J:127639
|
abnormal neuron differentiation
|
J:127639
|
Ngfrtm1Jae/Ngfrtm1Jae
(C;129S-Ngfrtm1Jae/J)
|
abnormal neuron apoptosis
|
J:46125
|
Ngfrtm1Jae/Ngfrtm1Jae
(B6.129S4-Ngfrtm1Jae)
|
abnormal axon extension
|
J:127639
|
abnormal neuron differentiation
|
J:127639
|
Ngfrtm1Jae/Ngfrtm1Jae
(involves: 129 * BALB/c)
|
abnormal axon extension
|
J:96121
|
Ngfrtm1Jae/Ngfrtm1Jae
(involves: 129S4/SvJae)
|
abnormal axon guidance
|
J:145459
|
decreased neuron apoptosis
|
J:123022
|
Ngfrtm1Jae/Ngfrtm1Jae
(involves: 129S4/SvJae * C57BL/6)
|
abnormal axon extension
|
J:139381
|
abnormal axon pruning
|
J:139381
|
Ngfrtm1Jae/Ngfrtm1Jae Ntf5tm1Jae/Ntf5tm1Jae
(involves: 129S4/SvJae)
|
decreased neuron apoptosis
|
J:123022
|
Ngfrtm1Jae/Ngfrtm1Jae Plgtm1Jld/Plgtm1Jld
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
increased hepatocyte apoptosis
|
J:120368
|
increased hepatocyte proliferation
|
J:120368
|
Ngfrtm1Jae/Ngfrtm1Jae Sema3atm1Mcf/Sema3atm1Mcf
(involves: 129S4/SvJae * C57BL/6)
|
abnormal neuron differentiation
|
J:127639
|
Ngly1tm1.1Tasuz/Ngly1tm1.1Tasuz
(B6.Cg-Ngly1tm1.1Tasuz)
|
abnormal cell physiology
|
J:217663
|
Nhej1tm1.1Ics/Nhej1tm1.1Ics
(involves: 129 * C57BL/6)
|
increased sensitivity to induced cell death
|
J:194422
|
increased thymocyte apoptosis
|
J:194422
|
Nhej1tm1.1Ics/Nhej1tm1.1Ics Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
decreased thymocyte apoptosis
|
J:194422
|
Nhej1tm1Fwa/Nhej1tm1Fwa
(129S6/SvEvTac-Nhej1tm1Fwa)
|
abnormal DNA repair
|
J:120145
|
increased cellular sensitivity to gamma-irradiation
|
J:120145
|
spontaneous chromosome breakage
|
J:120145
|
Nhej1tm1Fwa/Nhej1tm1Fwa
(involves: 129)
|
increased cellular sensitivity to gamma-irradiation
|
J:138774
|
spontaneous chromosome breakage
|
J:138774
|
Nherf1tm1Geo/Nherf1tm1Geo
(involves: C57BL/6J)
|
abnormal intestinal goblet cell morphology
|
J:95282
|
Nhlh2tm1Irk/Nhlh2tm1Irk
(involves: 129S4/SvJae * C57BL/6)
|
azoospermia
|
J:39356
|
decreased male germ cell number
|
J:39356
|
Nhlrc1tm1(KOMP)Vlcg/Nhlrc1tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
impaired autophagy
|
J:210491
|
Nhlrc1tm1(KOMP)Vlcg/Nhlrc1tm1(KOMP)Vlcg Gys1tm1c(EUCOMM)Wtsi/Gys1+ Tg(Nes-cre)1Kag/?
(involves: C57BL/6NTac)
|
abnormal autophagy
|
J:210491
|
Nhlrc1tm1(KOMP)Vlcg/Nhlrc1tm1(KOMP)Vlcg Gys1tm1c(EUCOMM)Wtsi/Gys1tm1c(EUCOMM)Wtsi Tg(Nes-cre)1Kag/?
(involves: C57BL/6NTac)
|
cellular phenotype
|
J:210491
|
Nhlrc1tm1.2Geno/Nhlrc1tm1.2Geno
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal autophagy
|
J:181559
|
Niban3tm1Jyw/Niban3tm1Jyw
(B6.Cg-Niban3tm1Jyw)
|
increased B cell proliferation
|
J:282961
|
Nicol1em1Osb/Nicol1em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
impaired sperm migration in female genital tract
|
J:335479
|
Nid1tm1Dong/Nid1tm1Dong
(involves: 129P2/OlaHsd)
|
abnormal basement membrane morphology
|
J:80843
|
Nid1tm1Ron/Nid1tm1Ron Nid2Gt(GST011)Byg/Nid2Gt(GST011)Byg
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:119014
|
Nid2Gt(GST011)Byg/Nid2Gt(GST011)Byg
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:78947
|
Nintm1d(EUCOMM)Hmgu/Nintm1d(EUCOMM)Hmgu
(involves: BALB/c * C57BL/6 * C57BL/6N)
|
abnormal mitotic spindle morphology
|
J:277726
|
Ninj1tm1b(KOMP)Wtsi/Ninj1+
(involves: C57BL/6N * FVB/N)
|
increased cellular sensitivity to gamma-irradiation
|
J:197409
|
Ninj1tm1b(KOMP)Wtsi/Ninj1tm1b(KOMP)Wtsi
(involves: C57BL/6N * FVB/N)
|
abnormal cellular replicative senescence
|
J:197409
|
Ninj1tm1Gto/Ninj1tm1Gto
(B6.129P2-Ninj1tm1Gto)
|
abnormal leukocyte adhesion
|
J:209516
|
impaired macrophage chemotaxis
|
J:209516
|
Ninj2em1Cqxu/Ninj2em1Cqxu
(C57BL/6-Ninj2em1Cqxu)
|
abnormal fat cell differentiation
|
J:332575
|
Nipal4tm1Akih/Nipal4tm1Akih
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal keratinocyte differentiation
|
J:261184
|
NipblGt(RRS564)Byg/Nipbl+
(involves: 129P2/OlaHsd * CD-1)
|
abnormal cell differentiation
|
J:154117
|
NipblGt(RRS564)Byg/Nipbl+
(involves: 129P2/OlaHsd * C57BL/6J * CD-1)
|
abnormal chromosome number
|
J:297059
|
abnormal DNA repair
|
J:297059
|
Nipbltm1.1Hpt/Nipbltm1.1Hpt H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S2/SvPas * C57BL/6 * C57BL/6J * CBA/J * SJL)
|
decreased cranial neural crest cell proliferation
|
J:213338
|
Nit1tm1Hbn/Nit1tm1Hbn
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell morphology
|
J:115052
|
decreased cellular sensitivity to gamma-irradiation
|
J:115052
|
Nkapltm1(KOMP)Vlcg/Nkapltm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
arrest of male meiosis
|
J:229252
|
azoospermia
|
J:229252
|
increased male germ cell apoptosis
|
J:229252
|
Nkd1tm1Tko/Nkd1tm1Tko
(involves: 129X1/SvJ)
|
oligozoospermia
|
J:95901
|
Nkx2-1tm1Jaw/Nkx2-1tm1Jaw
(involves: 129S2/SvPas * CD-1)
|
abnormal mesenchymal cell differentiation involved in lung development
|
J:85424
|
Nkx2-2tm1Jlr/Nkx2-2tm1Jlr
(involves: 129X1/SvJ)
|
abnormal pancreatic beta cell differentiation
|
J:48576
|
Nkx2-2tm2.1Suss/Nkx2-2tm2.1Suss Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ Tg(Ins2-cre)23Herr/0
(involves: 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA/J * SJL)
|
abnormal pancreatic beta cell differentiation
|
J:177838
|
Nkx2-2tm2.1Suss/Nkx2-2tm2.1Suss Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ Tg(Pdx1-cre/Esr1*)#Dam/0
(involves: 129S6/SvEvTac * Black Swiss * C57BL/6 * CBA * SJL)
|
abnormal pancreatic beta cell differentiation
|
J:177838
|
Nkx2-3tm1Hha/Nkx2-3tm1Hha
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell proliferation
|
J:54198
|
Nkx2-3tm1Hha/Nkx2-3tm1Hha
(involves: 129S4/SvJae)
|
abnormal leukocyte migration
|
J:62129
|
Nkx2-3tm1Rph/Nkx2-3tm1Rph
(involves: 129S1/Sv * C57BL/6)
|
abnormal leukocyte migration
|
J:64018
|
Nkx2-5tm1(cre)Rjs/Nkx2-5+ Tbx1tm1Bld/Tbx1tm3Bld
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased mitotic index
|
J:91013
|
Nkx2-5tm1.1Gum/Nkx2-5tm1.1Gum Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6J)
|
decreased cell proliferation
|
J:228275
|
increased apoptosis
|
J:228275
|
Nkx2-5tm1Siz/Nkx2-5tm1Siz
(involves: 129S4/SvJaeSor * C57BL/6J)
|
decreased cell proliferation
|
J:69976
|
Nkx2-5tm1Siz/Nkx2-5tm1Siz Nkx2-6tm1Siz/Nkx2-6tm1Siz
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J)
|
decreased cell proliferation
|
J:69976
|
increased apoptosis
|
J:69976
|
Nkx2-9tm1Hha/Nkx2-9tm1Hha
(involves: 129/Sv * C57BL/6)
|
abnormal axon guidance
|
J:102358
|
Nkx3-1tm1Hha/Nkx3-1tm1Hha
(involves: 129S4/SvJae * C57BL/6)
|
increased cell proliferation
|
J:63764
|
Nkx3-2tm1Tno/Nkx3-2tm1Tno
(involves: 129S4/SvJae * C57BL/6J)
|
decreased cell proliferation
|
J:77612
|
Nkx6-1tm1Jlr/Nkx6-1tm1.1Msan Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+ Tg(Ins2-cre)25Mgn/0
(involves: 129 * C57BL/6 * DBA * SJL)
|
abnormal pancreatic beta cell differentiation
|
J:195153
|
Nkx6-1tm1Jlr/Nkx6-1tm1.1Msan Tg(CAG-Bgeo/GFP)21Lbe/0 Tg(Neurog3-cre)C1Able/0
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal pancreatic beta cell differentiation
|
J:195153
|
Nkx6-2tm1Ercs/Nkx6-2+ Phox2btm1(Phox2a)Mist/Phox2b+
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
abnormal axon extension
|
J:126634
|
Nle1tm1Cba/Nle1tm1.1Cota Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S2/SvPas)
|
abnormal ribosome biogenesis
|
J:204063
|
Nle1tm1Cba/Nle1tm1Cba
(involves: 129S2/SvPas * C57BL/6 * SJL/J)
|
abnormal inner cell mass apoptosis
|
J:108385
|
NlnGt(NPX481)Byg/NlnGt(NPX481)Byg
(B6.129P2-NlnGt(NPX481)Byg)
|
abnormal cellular respiration
|
J:214116
|
Nlrc4tm1Vmd/Nlrc4tm1Vmd
(C57BL/6N-Nlrc4tm1Vmd)
|
abnormal cell death
|
J:91292
|
Nlrp1am1Btlr/Nlrp1am1Btlr
(C57BL/6J-Nlrp1am1Btlr)
|
increased macrophage apoptosis
|
J:265173
|
Nlrp1am2Btlr/Nlrp1am2Btlr
(C57BL/6J-Nlrp1am2Btlr)
|
increased macrophage apoptosis
|
J:265174
|
Nlrp2tm1.2Itl/Nlrp2tm1.2Itl
(involves: C57BL/6)
|
cellular phenotype
|
J:237496
|
maternal effect
|
J:237496
|
Nlrp2tm1a(KOMP)Wtsi/Nlrp2tm1a(KOMP)Wtsi
(Not Specified)
|
abnormal oocyte morphology
|
J:275254
|
maternal effect
|
J:275254
|
Nlrp3tm1Bhk/Nlrp3tm1Bhk
(B6.129S6-Nlrp3tm1Bhk/J)
|
oxidative stress
|
J:256504
|
Nlrp3tm3.1Hhf/Nlrp3+
(involves: 129)
|
abnormal osteoclast differentiation
|
J:202147
|
decreased cell proliferation
|
J:202147
|
Nlrp4fem1Lil/Nlrp4fem1Lil
(involves: CD-1)
|
abnormal oocyte morphology
|
J:284116
|
maternal effect
|
J:284116
|
Nlrp5tm1Zbt/Nlrp5tm1Zbt
(Not Specified)
|
abnormal microtubule cytoskeleton morphology
|
J:276268
|
maternal effect
|
J:65518
|
Nlrp5tm1Zbt/Nlrp5tm1Zbt OoepGt(139A2)Cmhd/OoepGt(139A2)Cmhd
(involves: 129S1/Sv * 129X1/SvJ)
|
maternal effect
|
J:140105
|
Nlrp5tm1Zbt/Nlrp5tm1Zbt OoepGt(139A2)Cmhd/OoepGt(139A2)Cmhd Tle6tm1Lil/Tle6tm1Lil
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal mitotic spindle morphology
|
J:276268
|
Nlrp6tm1Macha/Nlrp6tm1Macha
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal enterocyte proliferation
|
J:173352
|
Nlrp9bem1Flv/Nlrp9bem1Flv
(C57BL/6N-Nlrp9bem1Flv)
|
decreased apoptosis
|
J:243487
|
Nlrp12tm1Jpyt/Nlrp12tm1Jpyt
(B6.Cg-Nlrp12tm1Jpyt)
|
abnormal leukocyte migration
|
J:164725
|
impaired neutrophil chemotaxis
|
J:164725
|
Nlrp14em1Gfan/Nlrp14em1Gfan
(C57BL/6J-Nlrp14em1Gfan)
|
maternal effect
|
J:333868
|
Nme1tm1Jyd/Nme1tm1Jyd
(involves: 129/Sv * C57BL/6)
|
maternal effect
|
J:109190
|
Nme1tm1Jyd/Nme1tm1Jyd
(B6.129-Nme1tm1Jyd)
|
maternal effect
|
J:109190
|
Nme5tm1Lex/Nme5tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:185566
|
abnormal spermatid morphology
|
J:185566
|
azoospermia
|
J:185566
|
detached sperm flagellum
|
J:185566
|
Nme7Gt(OST31116)Lex/Nme7Gt(OST31116)Lex
(involves: 129S5/SvEvBrd * C57BL/6Brd)
|
abnormal respiratory motile cilium physiology
|
J:171184
|
Nme8tm1.1Arte/Nme8tm1.1Arte Txndc2tm1.1Arte/Txndc2tm1.1Arte
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal DNA repair
|
J:205172
|
asthenozoospermia
|
J:205172
|
oxidative stress
|
J:205172
|
Nmnat1tm1Ruch/Nmnat1tm1d(EUCOMM)Wtsi
(involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6J * C57BL/6N)
|
increased endoplasmic reticulum stress
|
J:267630
|
Nmnat2Gt(EUCE0262a08)Hmgu/Nmnat2Gt(EUCE0262a08)Hmgu
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal axon extension
|
J:200901
|
Nmt1tm1.1Poru/Nmt1tm1.1Poru Nmt2tm1.1Poru/Nmt2tm1.1Poru Tg(Lck-cre)1Cwi/0
(involves: C57BL/6 * DBA/2 * SJL)
|
decreased splenocyte proliferation
|
J:226234
|
decreased T cell proliferation
|
J:226234
|
increased T cell apoptosis
|
J:226234
|
Nnattm1.1Geno/Nnat+ Ins1tm1.1(cre)Thor/Ins1+
(involves: 129S2/SvPas * C57BL/6J)
|
maternal imprinting
|
J:265677
|
Nnattm1.2Geno/Nnat+
(either: 129S2(Cg)-Nnattm1.2Geno or B6.129S2(Cg)-Nnattm1.2Geno)
|
maternal imprinting
|
J:265677
|
NntG745D/NntG745D
(involves: BALB/c * C3H/HeH)
|
abnormal cell physiology
|
J:108421
|
NntN68K/NntN68K
(involves: BALB/c * C3H/HeH)
|
abnormal cell physiology
|
J:108421
|
Noa1tm1Tze/Noa1tm1Tze
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:176798
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:176798
|
abnormal mitochondrial crista morphology
|
J:176798
|
abnormal mitochondrial morphology
|
J:176798
|
abnormal mitochondrial physiology
|
J:176798
|
decreased apoptosis
|
J:176798
|
decreased embryonic tissue cell apoptosis
|
J:176798
|
decreased sensitivity to induced cell death
|
J:176798
|
Noboxtm1Rajk/Noboxtm1Rajk
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal oocyte morphology
|
J:92421
|
absent oocytes
|
J:92421
|
decreased oocyte number
|
J:92421
|
oocyte degeneration
|
J:92421
|
Noc2ltm1.1Arte/Noc2ltm1.1Arte Tg(CD2-icre)4Kio/0
(involves: C57BL/6 * C57BL/10 * CBA/Ca)
|
abnormal cell cycle
|
J:216490
|
abnormal T cell proliferation
|
J:216490
|
increased thymocyte apoptosis
|
J:216490
|
Noc3ltm1Maim/Noc3ltm1Maim
(B6J.B6NSlc-Noc3ltm1Maim)
|
abnormal cell nucleus count
|
J:210767
|
Noc4ltm1.1Nju/Noc4ltm1.1Nju
(involves: C57BL/6 * FVB/N)
|
increased embryonic tissue cell apoptosis
|
J:247476
|
Nod2tm1Daph/Nod2tm1Daph
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal autophagy
|
J:157879
|
Nod2tm1Flv/Nod2tm1Flv
(involves: 129S1/Sv)
|
impaired macrophage phagocytosis
|
J:147177
|
impaired neutrophil phagocytosis
|
J:147177
|
Nodaltm1.1Ysa/Nodaltm1.1Ysa Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal male germ cell morphology
|
J:191052
|
Nogtm1Amc/Nogtm1Amc
(involves: 129S1/Sv)
|
increased apoptosis
|
J:110617
|
Nol3tm1.1Rnkt/Nol3tm1.1Rnkt
(B6.129-Nol3tm1.1Rnkt)
|
decreased cell proliferation
|
J:193803
|
increased apoptosis
|
J:193803
|
Nol3tm1Rvh/Nol3tm1Rvh
(involves: C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:121501
|
NonoGt(YHA266)Byg/Y
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle
|
J:193286
|
delayed cellular replicative senescence
|
J:193286
|
increased fibroblast proliferation
|
J:193286
|
NonoGt(YHA266)Byg/Y
(involves: 129P2/OlaHsd)
|
cardiac interstitial fibrosis
|
J:294120
|
decreased fibroblast cell migration
|
J:294120
|
increased fibroblast proliferation
|
J:294120
|
Nos1tm1Enik/Nos1tm1Enik
(involves: 129X1/SvJ * C57BL/6)
|
abnormal neuron differentiation
|
J:99879
|
Nos1tm1Plh/Nos1tm1Plh
(involves: 129S4/SvJae * C57BL/6)
|
abnormal mitochondrial physiology
|
J:104558
|
Nos1tm1Plh/Nos1tm1Plh
(involves: 129S4/SvJae)
|
abnormal leukocyte adhesion
|
J:55936
|
decreased susceptibility to neuronal excitotoxicity
|
J:111644
|
enhanced leukocyte tethering or rolling
|
J:55936
|
Nos1tm1Plh/Nos1tm1Plh
(B6.129S4-Nos1tm1Plh)
|
decreased susceptibility to neuronal excitotoxicity
|
J:150557
|
maternal effect
|
J:57543
|
Nos1tm1Plh/Nos1tm1Plh
(B6;129S4-Nos1tm1Plh/J)
|
abnormal osteoclast differentiation
|
J:105612
|
Nos1tm1Plh/Nos1tm1Plh Nos2tm1Mrl/Nos2tm1Mrl Nos3tm1Plh/Nos3tm1Plh
(involves: 129S4/SvJae * 129S7/SvEvBrd)
|
increased renal tubule apoptosis
|
J:100308
|
Nos1tm1Plh/Nos1tm1Plh Nos3tm1Plh/Nos3tm1Plh
(B6.129S4-Nos3tm1Plh Nos1tm1Plh)
|
cardiac interstitial fibrosis
|
J:129064
|
Nos1aptm1Tsso/Nos1aptm1Tsso
(involves: C57BL/6JJcl)
|
oxidative stress
|
J:268528
|
Nos2tm1Lau/Nos2tm1Lau
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal male meiosis
|
J:84347
|
increased T cell proliferation
|
J:90903
|
Nos2tm1Lau/Nos2tm1Lau Tg(Thy1-APPSwDutIowa)BWevn/?
(involves: C57BL/6)
|
increased neuron apoptosis
|
J:132221
|
Nos2tm1Liew/Nos2tm1Liew
(involves: 129P2/Ola * MF1)
|
increased T cell proliferation
|
J:25755
|
Nos2tm1Mrl/Nos2tm1Mrl
(B6.129S7-Nos2tm1Mrl)
|
abnormal osteoclast differentiation
|
J:98070
|
Nos3tm1Plh/Nos3tm1Plh
(involves: 129S4/SvJae)
|
abnormal leukocyte adhesion
|
J:55936
|
enhanced leukocyte tethering or rolling
|
J:55936
|
increased susceptibility to neuronal excitotoxicity
|
J:111644
|
Nos3tm1Plh/Nos3tm1Plh
(involves: 129S4/SvJae * C57BL/6)
|
abnormal female meiosis
|
J:89702
|
abnormal neuronal precursor proliferation
|
J:101302
|
abnormal oocyte morphology
|
J:89702
|
abnormal oogenesis
|
J:89702
|
abnormal osteoblast physiology
|
J:67336
|
abnormal primary polar body morphology
|
J:89702
|
maternal effect
|
J:89702
|
Nos3tm1Unc/Nos3tm1Unc
(B6.129P2-Nos3tm1Unc/J)
|
abnormal osteoblast physiology
|
J:129477
|
abnormal redox activity
|
J:98094
|
decreased kidney cell proliferation
|
J:148626
|
increased fetal cardiomyocyte apoptosis
|
J:103270
|
increased kidney apoptosis
|
J:148626
|
increased mesangial cell number
|
J:148626
|
increased renal tubule apoptosis
|
J:117046
|
Nostrintm1.1Oess/Nostrintm1.1Oess
(B6.129S2(Cg)-Nostrintm1.1Oess)
|
abnormal vascular endothelial cell migration
|
J:188414
|
decreased vascular endothelial cell proliferation
|
J:188414
|
Nostrintm1Oess/Nostrintm1Oess Tg(Tek-cre)12Flv/0
(involves: 129S2/SvPas * C3H * C57BL/6)
|
abnormal vascular endothelial cell migration
|
J:188414
|
decreased vascular endothelial cell proliferation
|
J:188414
|
Notch1tm1Agt/Notch1tm1Agt Tg(Tek-cre)1Ywa/0
(involves: 129 * C57BL/6 * SJL)
|
increased apoptosis
|
J:100449
|
Notch1tm1Agt/Notch1tm1Agt Tg(Tek-cre)12Flv/0
(involves: 129 * C3H * C57BL/6)
|
increased apoptosis
|
J:100449
|
Notch1tm1Con/Notch1tm1Con
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
abnormal cell death
|
J:25248
|
Notch1tm1Grid/Notch1+ Notch3tm1Grid/Notch3tm1Grid
(involves: 129S1/Sv * C57BL/6)
|
impaired basement membrane formation
|
J:227333
|
Notch1tm2Pst/Notch1tm2Pst
(B6.Cg-Notch1tm2Pst)
|
increased T cell apoptosis
|
J:131563
|
Notch1tm2Rko/Notch1tm2Rko Tg(Nes-cre)1Kln/0
(involves: 129X1/SvJ * C57BL/6J * SJL)
|
abnormal apoptosis
|
J:90392
|
Notch2tm1.1Ecan/Notch2+
(involves: 129 * 129S1/Sv * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:230045
|
Notch2tm1.1Hhtg/Notch2+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:311038
|
Notch2tm1Grid/Notch2tm1Grid
(involves: 129S1/Sv * C57BL/6J)
|
absent mesangial cell
|
J:67157
|
decreased kidney cell proliferation
|
J:67157
|
increased kidney apoptosis
|
J:67157
|
Notch2tm1Yha/Notch2tm1Yha
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:55841
|
Notch2tm3Grid/Notch2tm3Grid Foxg1tm1(cre)Skm/Foxg1+
(involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6)
|
increased apoptosis
|
J:130929
|
increased neuron apoptosis
|
J:130929
|
Notch2tm3Grid/Notch2tm3Grid Tg(Pax3-cre)1Joe/0
(involves: 129S1/Sv)
|
abnormal cell cycle
|
J:119907
|
cellular phenotype
|
J:119907
|
Notch3em1Ecan/Notch3+
(C57BL/6J-Notch3em1Ecan)
|
abnormal osteoclast differentiation
|
J:270682
|
increased osteoblast proliferation
|
J:270682
|
Nototm1Gos/Nototm1Gos
(involves: 129S1/SvImJ)
|
abnormal embryonic cilium location or orientation
|
J:182741
|
abnormal motile primary cilium morphology
|
J:182741
|
absent nodal flow
|
J:182741
|
decreased embryonic cilium length
|
J:182741
|
Nototm2.1(Foxj1)Gos/Nototm2.1(Foxj1)Gos
(involves: C57BL/6 * SJL)
|
abnormal embryonic cilium location or orientation
|
J:182741
|
abnormal motile primary cilium morphology
|
J:182741
|
abnormal motile primary cilium physiology
|
J:182741
|
Nova1tm1Rbd/Nova1tm1Rbd
(Not Specified)
|
increased neuron apoptosis
|
J:60771
|
Nox1tm1.1Anrt/Nox1tm1.1Anrt Tg(Vil1-cre)997Gum/0
(involves: C57BL/6J * SJL)
|
abnormal redox activity
|
J:194294
|
Nox1tm1Cyn/Y
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal redox activity
|
J:218649
|
decreased cell migration
|
J:218649
|
Nox4tm1.1Ams/Nox4tm1.1Ams
(B6.129-Nox4tm1.1Ams)
|
cardiac interstitial fibrosis
|
J:165541
|
Nox4tm1.1Hwsc/Nox4tm1.1Hwsc
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased neuron apoptosis
|
J:166948
|
oxidative stress
|
J:166948
|
Nox4tm1.1Jusa/Nox4tm1.1Jusa Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6 * FVB)
|
abnormal mitochondrial physiology
|
J:163751
|
cardiac interstitial fibrosis
|
J:163751
|
decreased cardiomyocyte apoptosis
|
J:163751
|
oxidative stress
|
J:163751
|
Nox4tm1Kkr/Nox4tm1Kkr
(B6.129-Nox4tm1Kkr)
|
decreased apoptosis
|
J:199354
|
oxidative stress
|
J:199354
|
Nox4tm1Syb/Nox4tm1Syb
(involves: 129S4/SvJae * C57BL/6N)
|
abnormal redox activity
|
J:218649
|
Nox4tm1Syb/Nox4tm1Syb
(involves: 129S4/SvJae)
|
decreased kidney apoptosis
|
J:298830
|
decreased renal tubule apoptosis
|
J:298830
|
Npas4tm1Ooe/Npas4tm1Ooe
(involves: 129/Sv * C57BL/6)
|
increased susceptibility to neuronal excitotoxicity
|
J:145569
|
Npc1m1N/Npc1m1N
(involves: BALB/c)
|
abnormal cellular cholesterol metabolism
|
J:104996
|
abnormal Golgi apparatus morphology
|
J:267948
|
abnormal sperm head morphology
|
J:119302
|
absent sperm flagellum
|
J:119302
|
absent sperm head
|
J:119302
|
oligozoospermia
|
J:119302
|
teratozoospermia
|
J:119302
|
Npc1m1N/Npc1m1N
(BALB/cNctr-Npc1m1N/J)
|
abnormal cellular cholesterol metabolism
|
J:149812
|
abnormal lysosome physiology
|
J:209834
|
abnormal mitochondrial crista morphology
|
J:98011
|
abnormal mitochondrial matrix morphology
|
J:98011
|
abnormal mitochondrial morphology
|
J:98011
|
abnormal mitochondrial physiology
|
J:98011
|
abnormal mitochondrial shape
|
J:98011
|
Npc1m1N/Npc1m1N
(B6.C-Npc1m1N)
|
foam cell reticulosis
|
J:157113
|
Npc1m1N/Npc1m1N
(BALB/c-Npc1m1N)
|
abnormal primary cilium morphology
|
J:242832
|
increased macrophage derived foam cell number
|
J:221855
|
Npc1m1N/Npc1tm1.2Apl
(B6.Cg-Npc1m1N/Npc1tm1.2Apl)
|
foam cell reticulosis
|
J:157113
|
Npc1nmf164/Npc1nmf164
(C57BL/6J-Npc1nmf164/J)
|
abnormal cellular cholesterol metabolism
|
J:179744
|
increased macrophage derived foam cell number
|
J:179744
|
sphingomyelinosis
|
J:179744
|
Npc1spm/Npc1spm
(C57BLKS/J-Npc1spm/J)
|
abnormal plasma membrane sphingolipid content
|
J:7245
|
increased macrophage derived foam cell number
|
J:7245
|
increased plasma membrane sphingolipid content
|
J:7245
|
sphingomyelinosis
|
J:7245
|
Npc1tm1.1Dso/Npc1tm1.1Dso
(B6.129-Npc1tm1.1Dso)
|
increased macrophage derived foam cell number
|
J:221855
|
sphingomyelinosis
|
J:221855
|
Npc1tm1Mbjg/Npc1tm1Mbjg
(involves: 129S6/SvEvTac * C57BL/6J)
|
foam cell reticulosis
|
J:176587
|
Npc2tm1Plob/Npc2tm1Plob
(C.129S1-Npc2tm1Plob)
|
abnormal lysosome morphology
|
J:125609
|
Npeppsgoku/Npeppsgoku
(involves: 129P2/OlaHsd * BALB/cA)
|
asthenozoospermia
|
J:69615
|
decreased elongated spermatid number
|
J:69615
|
oligozoospermia
|
J:69615
|
Npffr2tm1.2Ics/Npffr2tm1.2Ics
(involves: C57BL/6N)
|
decreased macrophage proliferation
|
J:245025
|
Nphp1em1Lisu/Nphp1em1Lisu
(C57BL/6J-Nphp1em1Lisu)
|
decreased male germ cell number
|
J:324503
|
Nphp1tm1.1Hung/Nphp1tm1.1Hung
(B6.Cg-Nphp1tm1.1Hung)
|
abnormal sperm flagellum morphology
|
J:140205
|
decreased male germ cell number
|
J:140205
|
oligozoospermia
|
J:140205
|
teratozoospermia
|
J:140205
|
Nphp3pcy/Nphp3tm1Cbe
(involves: C57BL/6 * CD-1 * KK/Upj)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:139258
|
Nphp4nmf192/Nphp4nmf192
(involves: C57BL/6J)
|
abnormal retina apoptosis
|
J:167232
|
asthenozoospermia
|
J:167232
|
oligozoospermia
|
J:167232
|
Nphs1tm1Ktry/Nphs1tm1Ktry
(involves: 129X1/SvJ * C57BL/6)
|
increased mesangial cell number
|
J:66970
|
Nphs2tm1Antc/Nphs2tm3.1Antc Tg(CAG-cre/Esr1*)86Lbgn/0
(involves: 129 * C57BL/6 * DBA)
|
increased mesangial cell number
|
J:166320
|
Nplem1Avps/Nplem1Avps
(C57BL/6-Nplem1Avps)
|
abnormal cellular respiration
|
J:342764
|
abnormal oxidative phosphorylation
|
J:342764
|
increased mitochondrial number
|
J:342764
|
Nplem2Avps/Nplem2Avps
(C57BL/6-Nplem2Avps)
|
abnormal cellular respiration
|
J:342764
|
abnormal oxidative phosphorylation
|
J:342764
|
increased mitochondrial number
|
J:342764
|
Npm1Gt(VICTR37)704Lex/Npm1Gt(VICTR37)704Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell proliferation
|
J:101353
|
increased apoptosis
|
J:101353
|
increased fibroblast apoptosis
|
J:101353
|
Npm1Gt(VICTR37)704Lex/Npm1Gt(VICTR37)704Lex Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * 129S5/SvEvBrd * C57BL/6)
|
abnormal apoptosis
|
J:101353
|
increased fibroblast proliferation
|
J:101353
|
Npm1tm1Hft/Npm1+
(involves: 129)
|
abnormal granulocyte differentiation
|
J:194999
|
Npm1tm1Ppp/Npm1+
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell proliferation
|
J:101494
|
chromosome breakage
|
J:101494
|
Npm1tm1Ppp/Npm1+ Trp53tm1Brd/Trp53tm1Brd
(involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6)
|
increased fibroblast proliferation
|
J:101494
|
Npm1tm1Ppp/Npm1tm1Ppp
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell cycle
|
J:101494
|
decreased fibroblast proliferation
|
J:101494
|
increased embryonic tissue cell apoptosis
|
J:101494
|
Npm1tm2Ppp/Npm1tm2Ppp
(involves: 129S1/Sv * C57BL/6)
|
chromosome breakage
|
J:101494
|
decreased fibroblast proliferation
|
J:101494
|
Npm2tm1Zuk/Npm2tm1Zuk
(involves: 129 * C57BL/6J)
|
abnormal oocyte morphology
|
J:83658
|
Nppclbab/Nppclbab
(B6.PL-Nppclbab/GrsrJ)
|
abnormal female meiosis
|
J:164870
|
Npr1tm1Gar/Npr1tm1Gar
(B6.129S7-Npr1tm1Gar)
|
impaired neutrophil chemotaxis
|
J:70496
|
Npr1tm1Kuhn/Npr1tm1Kuhn Tg(Myh6-cre)2182Mds/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
cardiac interstitial fibrosis
|
J:83298
|
Npr1tm1Mae/Npr1tm1Mae
(involves: 129P2/OlaHsd * C57BL/6)
|
cardiac interstitial fibrosis
|
J:74420
|
Npr2cn-2J/Npr2cn-2J
(B6;CBACa Aw-J/A-Npr2cn-2J/GrsrJ)
|
abnormal female meiosis
|
J:164870
|
Npr2pwe/Npr2pwe
(involves: C3H/HeJ * C57BL/6 * NAW/WI)
|
abnormal oogenesis
|
J:188839
|
Npy1rtm1.1Wpg/Npy1rtm1.1Wpg
(involves: 129X1/SvJ * C57BL/6)
|
abnormal neuron differentiation
|
J:92582
|
Npy1rtm1Tped/Npy1rtm1Tped
(B6.129P2-Npy1rtm1Tped)
|
cardiac interstitial fibrosis
|
J:101870
|
increased adipocyte glucose uptake
|
J:102554
|
Npy1rtm1Wpg/Npy1rtm1Wpg Tg(Col1a1-cre)2Bek/0
(involves: CD-1)
|
abnormal osteoblast physiology
|
J:170291
|
Npy2rtm1.1Hhz/Npy2rtm1.1Hhz Npy4rtm1.1Hhz/Npy4rtm1.1Hhz
(involves: 129X1/SvJ * BALB/cJ * C57BL/6)
|
abnormal osteoblast physiology
|
J:84570
|
Nqo1tm1Akj/Nqo1tm1Akj
(involves: C57BL/6)
|
abnormal redox activity
|
J:120478
|
Nqo1tm1Msho/Nqo1tm1Msho
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell physiology
|
J:151045
|
nr/nr
(BALB/cGr-nr)
|
abnormal mitochondrial morphology
|
J:5597
|
abnormal Purkinje cell mitochondrial morphology
|
J:5339
|
Nr0b1tm1.1Lja/Y
(involves: 129S1/Sv * 129X1/SvJ)
|
absent germ cells
|
J:51292
|
decreased male germ cell number
|
J:51292
|
increased Sertoli cell proliferation
|
J:71710
|
retention of the adrenal gland x-zone
|
J:51292
|
Nr1d1tm1Ven/Nr1d1tm1Ven
(Not Specified)
|
abnormal Purkinje cell differentiation
|
J:60839
|
Nr1d1tm1Ven/Nr1d1tm1Ven
(B6.Cg-Nr1d1tm1Ven)
|
increased adipocyte glucose uptake
|
J:203422
|
Nr1h2tm1.1Gstr/Nr1h2tm1.1Gstr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cellular cholesterol metabolism
|
J:82096
|
Nr1h2tm1.1Gstr/Nr1h2tm1.1Gstr Nr1h3tm1.1Gstr/Nr1h3tm1.1Gstr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased macrophage derived foam cell number
|
J:81790,
J:234268
|
Nr1h2tm1.1Nph/Nr1h2tm1.1Nph
(B6.129-Nr1h2tm1.1Nph)
|
abnormal cellular cholesterol metabolism
|
J:169945
|
increased muscle cell glucose uptake
|
J:169945
|
Nr1h2tm1Djm/Nr1h2tm1Djm
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal spermatogonia proliferation
|
J:120913
|
Nr1h2tm1Djm/Nr1h2tm1Djm Nr1h3tm1Djm/Nr1h3tm1Djm
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal spermatogonia proliferation
|
J:120913
|
increased male germ cell apoptosis
|
J:120913
|
Nr1h3tm1.1Gstr/Nr1h3tm1.1Gstr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cellular cholesterol metabolism
|
J:82096
|
Nr1h3tm1Djm/Nr1h3tm1Djm
(involves: 129S6/SvEvTac * C57BL/6)
|
increased male germ cell apoptosis
|
J:120913
|
Nr1h4tm1.2Auw/Nr1h4tm1.2Auw
(involves: 129 * C57BL/6J)
|
increased hepatocyte apoptosis
|
J:157882
|
increased hepatocyte proliferation
|
J:157882
|
Nr1h4tm1Gonz/Nr1h4tm1Gonz
(involves: 129X1/SvJ * C57BL/6N)
|
increased hepatocyte apoptosis
|
J:121075
|
increased hepatocyte proliferation
|
J:121075
|
Nr1h4tm1Gonz/Nr1h4tm1Gonz
(involves: 129X1/SvJ * C57BL/6)
|
increased hepatocyte apoptosis
|
J:118204
|
Nr1i2tm1Sakl/Nr1i2tm1Sakl
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased hepatocyte proliferation
|
J:157882
|
Nr1i3tm1Dgen/Nr1i3tm1Dgen
(B6.129-Nr1i3tm1Dgen)
|
abnormal lipid oxidation
|
J:149091
|
Nr2c2tm1Chc/Nr2c2tm1Chc
(Not Specified)
|
arrest of male meiosis
|
J:91602
|
increased granulosa cell apoptosis
|
J:133000
|
multinucleated giant male germ cells
|
J:121628
|
oligozoospermia
|
J:91602
|
Nr2e1frc/Nr2e1frc
(involves: 129P2/OlaHsd * 129S1/SvImJ)
|
abnormal neuronal precursor proliferation
|
J:183689
|
Nr2e1tm1Rev/Nr2e1tm1Rev Tg(CAG-cre/Esr1*)5Amc/?
(involves: C57BL/6 * CBA)
|
abnormal neuron differentiation
|
J:132664
|
Nr2e1tm1Rev/Nr2e1tm1Rtyu
(Not Specified)
|
abnormal neuron differentiation
|
J:132664
|
Nr2e1tm1Rtyu/Nr2e1tm1Rtyu
(Not Specified)
|
abnormal axon fasciculation
|
J:81762
|
decreased radial glial cell number
|
J:81762
|
Nr2e3rd7/Nr2e3rd7
(B6.Cg-Nr2e3rd7/J)
|
increased retina apoptosis
|
J:148636
|
Nr2f1tm1Mist/Nr2f1tm1Mist
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal axon guidance
|
J:114098
|
Nr2f1tm1Mjts/Nr2f1tm1Mjts
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal axon guidance
|
J:42259
|
Nr2f1tm1Mjts/Nr2f1tm1Mjts
(involves: 129S7/SvEvBrd)
|
abnormal organ of Corti supporting cell differentiation
|
J:112461
|
Nr3c1tm1.1Jda/Nr3c1+ Tg(Lck-cre)548Jxm/0
(B6.Cg-Nr3c1tm1.1Jda Tg(Lck-cre)548Jxm)
|
decreased thymocyte apoptosis
|
J:189951
|
Nr3c1tm1.1Jda/Nr3c1tm1.1Jda Tg(Lck-cre)548Jxm/0
(B6.Cg-Nr3c1tm1.1Jda Tg(Lck-cre)548Jxm)
|
decreased thymocyte apoptosis
|
J:189951
|
Nr3c1tm1Ljm/Nr3c1tm1Ljm
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal thymocyte apoptosis
|
J:82174
|
Nr3c1tm2.1Gsc/Nr3c1+
(B6.129P2-Nr3c1tm2.1Gsc)
|
decreased T cell apoptosis
|
J:126427
|
Nr3c1tm2.1Gsc/Nr3c1tm2.1Gsc
(involves: 129P2/OlaHsd * 129X1/SvJ)
|
abnormal osteoblast differentiation
|
J:160669
|
abnormal osteoblast physiology
|
J:160669
|
Nr3c1tm2.1Ljm/Nr3c1tm2.1Ljm Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S6/SvEvTac)
|
decreased susceptibility to neuronal excitotoxicity
|
J:197150
|
Nr3c1tm2Gsc/Nr3c1tm2Gsc Tg(Lck-cre)I57Jxm/0
(B6.Cg-Nr3c1tm2Gsc Tg(Lck-cre)I57Jxm)
|
decreased T cell apoptosis
|
J:137157
|
Nr3c1tm2Gsc/Nr3c1tm2Gsc Tg(Runx2-icre)1Jtuc/0
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal osteoblast differentiation
|
J:160669
|
Nr3c1tm3Gsc/Nr3c1tm3Gsc
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal osteoblast physiology
|
J:160669
|
Nr3c2tm1.1Ics/Nr3c2tm1.1Ics Tg(Acta2-cre/ERT2)#Pcn/0
(involves: 129S2/SvPas * FVB/N)
|
abnormal redox activity
|
J:193438
|
Nr4a1tm1Jmi/Nr4a1tm1Jmi
(involves: 129S2/SvPas)
|
decreased B cell apoptosis
|
J:306652
|
increased B cell proliferation
|
J:306652
|
Nr4a1tm1Pcn/Nr4a1tm1Pcn Tg(Cr2-cre)3Cgn/0
(involves: 129)
|
increased B cell proliferation
|
J:306652
|
Nr4a2tm1Omc/Nr4a2tm1Omc
(involves: 129S7/SvEvBrd * C57BL/6)
|
increased midbrain apoptosis
|
J:46856
|
Nr4a2tm1Tpe/Nr4a2+ Nr4a3tm1Dgen/Nr4a3tm1Dgen
(involves: 129P2/OlaHsd)
|
increased susceptibility to neuronal excitotoxicity
|
J:162076
|
oxidative stress
|
J:162076
|
Nr4a3tm1Omc/Nr4a3tm1Omc
(involves: 129S/SvEv * C57BL/6)
|
abnormal axon extension
|
J:93320
|
abnormal axon guidance
|
J:93320
|
increased neuron apoptosis
|
J:93320
|
Nr5a1tm1.1Hain/Nr5a1+
(Not Specified)
|
retention of the adrenal gland x-zone
|
J:175843
|
Nr5a1tm1.1Hain/Nr5a1tm1.1Hain
(Not Specified)
|
oligozoospermia
|
J:175843
|
retention of the adrenal gland x-zone
|
J:175843
|
Nr5a1tm1Klp/Nr5a1tm1Klp
(involves: 129P2/OlaHsd * C57BL/6 * FVB)
|
abnormal neuron differentiation
|
J:83384
|
Nr5a1tm2Klp/Nr5a1tm2.1Klp Tg(Cga-cre)3Sac/0
(involves: 129P2/OlaHsd * C57BL/6J * SJL)
|
decreased elongated spermatid number
|
J:66593
|
decreased male germ cell number
|
J:66593
|
Nr6a1tm3Coo/Nr6a1tm3Coo Tg(Zp3-cre)93Knw/0
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal oocyte morphology
|
J:85054
|
Nrarptm1Vlcg/Nrarp+
(involves: C57BL/6J)
|
abnormal vascular regression
|
J:144980
|
Nrarptm1Vlcg/Nrarptm1Vlcg
(involves: C57BL/6J)
|
abnormal vascular regression
|
J:144980
|
decreased vascular endothelial cell proliferation
|
J:144980
|
Nrastm1.1Emfu/Nrastm1.1Emfu
(involves: 129S1/Sv * FVB/N)
|
abnormal granulocyte differentiation
|
J:189834
|
Nrastm1Tyj/Nrastm1Tyj Tg(Tyr-cre)1Lru/0
(involves: C57BL/6 * DBA/2)
|
abnormal melanocyte proliferation
|
J:198244
|
Nrbf2Gt(Ayu21-W143)Imeg/Nrbf2Gt(Ayu21-W143)Imeg
(involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal autophagosome formation
|
J:220500
|
impaired autophagy
|
J:220500
|
increased hepatocyte apoptosis
|
J:220500
|
increased sensitivity to induced cell death
|
J:220500
|
Nrbp1tm1.1Dja/Nrbp1tm1.1Dja Gt(ROSA)26Sortm1(cre/ERT)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
abnormal enterocyte proliferation
|
J:184685
|
abnormal intestinal goblet cell morphology
|
J:184685
|
Nrbp1tm1.1Dja/Nrbp1tm1.2Dja Gt(ROSA)26Sortm1(cre/ERT)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6J)
|
abnormal enterocyte proliferation
|
J:184685
|
abnormal intestinal goblet cell morphology
|
J:184685
|
Nrbp1tm1.1Dja/Nrbp1tm1.2Dja Lgr5tm1(cre/ERT2)Cle/Lgr5+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
abnormal intestinal goblet cell morphology
|
J:184685
|
Nrf1tm1c(KOMP)Wtsi/Nrf1tm1c(KOMP)Wtsi Tg(Rho-icre)1Ck/0
(involves: C57BL/6N * SJL)
|
abnormal mitochondrial morphology
|
J:267504
|
abnormal mitochondrial physiology
|
J:267504
|
decreased mitochondrial size
|
J:267504
|
increased mitochondrial number
|
J:267504
|
Nrf1tm1c(KOMP)Wtsi/Nrf1tm1c(KOMP)Wtsi Tg(Six3-cre)69Frty/0
(involves: C57BL/6N * DBA/2)
|
abnormal axon extension
|
J:267504
|
Nrf1tm1Rcs/Nrf1tm1Rcs
(involves: 129X1/SvJ)
|
abnormal mitochondrial morphology
|
J:67376
|
decreased cell proliferation
|
J:67376
|
Nrg1tm1Cbm/Nrg1tm1Cbm
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased radial glial cell number
|
J:82745
|
Nrg1tm1Cbm/Nrg1tm1Cbm
(involves: 129P2/OlaHsd)
|
abnormal neural crest cell migration
|
J:48515
|
Nrg1tm1Lwr/Nrg1tm1Lwr
(129/Sv-Nrg1tm1Lwr)
|
defasiculated phrenic nerve
|
J:60159
|
Nrg1tm1Sabe/Nrg1tm1Sabe Tg(Amh-cre/ERT)#Sabe/0
(B6JJcl.Cg-Nrg1tm1Sabe Tg(Amh-cre/ERT)#Sabe)
|
abnormal male germ cell apoptosis
|
J:175448
|
azoospermia
|
J:175448
|
Nrg1tm2Cbm/Nrg1tm2Cbm
(involves: 129P2/OlaHsd)
|
abnormal neural crest cell migration
|
J:48515
|
Nrip1tm1Mpk/Nrip1tm1Mpk
(involves: 129/Ola)
|
abnormal oocyte morphology
|
J:74971
|
Nrip1tm1Mpk/Nrip1tm1Mpk
(involves: 129 * C57BL/6J)
|
abnormal enterocyte proliferation
|
J:211324
|
increased enterocyte apoptosis
|
J:211324
|
Nrn1tm1.2Ndiv/Nrn1tm1.2Ndiv
(C57BL/6-Nrn1tm1.2Ndiv)
|
delayed axon extension
|
J:178970
|
Nrp1tm1Ddg/Nrp1tm1Ddg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal axon guidance
|
J:93799
|
Nrp1tm1Hfu/Nrp1tm1Hfu
(involves: CD-1 * JF1)
|
delayed neuronal migration
|
J:94050
|
Nrp1tm1Hfu/Nrp1tm1Hfu
(involves: C57BL/6 * CBA)
|
abnormal axon guidance
|
J:98330
|
Nrp2tm1.2Mom/Nrp2tm1.2Mom
(involves: 129P2/OlaHsd * C57BL/6 * SJL/J)
|
abnormal axon guidance
|
J:76686
|
Nrp2tm1Ddg/Nrp2tm1Ddg
(involves: C57BL/6)
|
decreased cell proliferation
|
J:156869
|
Nrp2tm1Mkl/Nrp2tm1Mkl
(involves: ICR)
|
abnormal neuronal migration
|
J:134616
|
Nrrostm1Lex/Nrrostm1Lex
(B6.129S5-Nrrostm1Lex)
|
oxidative stress
|
J:209569
|
Nsmce2Gt(AA0032)Wtsi/Nsmce2+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell nucleus morphology
|
J:227197
|
abnormal mitosis
|
J:227197
|
elevated level of mitotic sister chromatid exchange
|
J:227197
|
increased cell nucleus count
|
J:227197
|
Nsmce2Gt(AA0032)Wtsi/Nsmce2Gt(AA0032)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell mass
|
J:227197
|
abnormal cell nucleus morphology
|
J:227197
|
abnormal chromosome morphology
|
J:227197
|
Nsmce2tm2.1Ofc/Nsmce2tm2.1Ofc Ndor1Tg(UBC-cre/ERT2)1Ejb/0
(involves: 129S/SvEv * C57BL/6 * SJL)
|
abnormal cell nucleus morphology
|
J:227197
|
abnormal mitosis
|
J:227197
|
elevated level of mitotic sister chromatid exchange
|
J:227197
|
mitotic nondisjunction
|
J:227197
|
Nsrp1tm1.1Cdj/Nsrp1tm1.1Cdj Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * DBA/2 * SJL)
|
increased T cell apoptosis
|
J:306261
|
increased T cell proliferation
|
J:306261
|
Nsun2tm1a(EUCOMM)Wtsi/Nsun2tm1a(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
oligozoospermia
|
J:213427
|
Nsun3tm1.1Tomik/Nsun3tm1.1Tomik Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6 * C57BL/6J * FVB/N)
|
abnormal mitochondrial physiology
|
J:336777
|
abnormal myocardial fiber mitochondrial morphology
|
J:336777
|
Nsun4tm1.2Arte/Nsun4tm1.2Arte Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6 * FVB/N * SJL)
|
abnormal mitochondrial physiology
|
J:211012
|
abnormal oxidative phosphorylation
|
J:211012
|
increased mitochondrial DNA content
|
J:211012
|
Nsun7Ste5Jcs1/Nsun7Ste5Jcs1
(involves: C3HeB/FeJ * C57BL/6)
|
asthenozoospermia
|
J:100332
|
Nsun7Ste5Jcs1/Nsun7Ste5Jcs1
(involves: C57BL/6)
|
abnormal sperm midpiece morphology
|
J:124143
|
abnormal sperm mitochondrial sheath morphology
|
J:124143
|
abnormal sperm motility
|
J:124143
|
Ntan1tm1Avar/Ntan1tm1Avar
(involves: 129)
|
decreased splenocyte proliferation
|
J:62140
|
Ntf5tm1Jae/Ntf5tm1Jae
(involves: 129S4/SvJae)
|
decreased neuron apoptosis
|
J:123022
|
Ntf5tm1Par/Ntf5tm1Par
(involves: 129S1/Sv * C57BL/6)
|
abnormal neuron differentiation
|
J:60927
|
Nthl1tm1Tbor/Nthl1tm1Tbor
(involves: 129X1/SvJ * C57BL/6)
|
abnormal DNA repair
|
J:78429
|
cellular phenotype
|
J:78429
|
Nthl1tm1Yas/Nthl1tm1Yas
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal DNA repair
|
J:77767
|
Ntmt1tm1(NCOM)Mfgc/Ntmt1tm1(NCOM)Mfgc
(involves: C57BL/6J * C57BL/6NCrl)
|
abnormal mitochondrial physiology
|
J:239287
|
increased cellular sensitivity to oxidative stress
|
J:239287
|
oxidative stress
|
J:239287
|
Ntn1Gt(ST629)Byg/Ntn1Gt(ST629)Byg Slit2tm1Matl/Slit2tm1Matl
(involves: 129P2/OlaHsd * 129S2/SvPas)
|
abnormal cell adhesion
|
J:106011
|
Ntn1tm1.2Tek/Ntn1tm1.2Tek
(involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * SJL)
|
abnormal axon guidance
|
J:227232
|
Ntn4tm1Wjbr/Ntn4tm1Wjbr
(B6.129-Ntn4tm1Wjbr)
|
increased cell proliferation
|
J:196758
|
Ntn4tm1Wjbr/Ntn4tm1Wjbr Tg(Thy1-YFP)HJrs/0
(B6.Cg-Ntn4tm1Wjbr Tg(Thy1-YFP)HJrs)
|
abnormal axon fasciculation
|
J:196758
|
Ntrk1em1Krvl/Ntrk1em1Krvl
(C57BL/6J-Ntrk1em1Krvl)
|
abnormal axon extension
|
J:338830
|
increased neuron apoptosis
|
J:338830
|
Ntrk2tm1Bxu/Ntrk2tm1Bxu
(involves: 129 * C57BL/6)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:170724
|
Ntrk2tm1Rohr/Ntrk2tm1Rohr
(Not Specified)
|
decreased granulosa cell proliferation
|
J:88782
|
impaired granulosa cell differentiation
|
J:88782
|
Ntrk2tm2.1Mini/Ntrk2tm2.1Mini
(involves: 129P2/OlaHsd)
|
abnormal axon fasciculation
|
J:132562
|
abnormal neuron differentiation
|
J:132562
|
abnormal neuronal migration
|
J:132562
|
Ntrk2tm2.1Tes/Ntrk2tm2.1Tes
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal axon extension
|
J:193542
|
Ntrk2tm2Kln/Ntrk2tm2Kln Slc1a3tm1(cre/ERT2)Mgoe/? Gt(ROSA)26Sortm1Sor/?
(involves: 129S2/SvPas * 129S4/SvJaeSor * C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:143452
|
Ntrk2tm2Kln/Ntrk2tm2Kln Tg(Nes-cre)1Kln/0
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal axon fasciculation
|
J:132562
|
abnormal neuron differentiation
|
J:132562
|
abnormal neuronal migration
|
J:132562
|
Nuak1tm1Esu/Nuak1tm1Esu Tg(Ckmm-cre)5Khn/0
(B6.Cg-Nuak1tm1Esu Tg(Ckmm-cre)5Khn)
|
abnormal skeletal muscle cell glucose uptake
|
J:185463
|
Nubp2tm1c(EUCOMM)Hmgu/Nubp2tm1c(EUCOMM)Hmgu Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ Tg(Wnt1-GAL4)11Rth/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA/J)
|
increased cranial neural crest cell apoptosis
|
J:284772
|
Nubplem1Vkim/Nubpltm1a(KOMP)Wtsi
(C57BL/6N-Nubplem1Vkim Nubpltm1a(KOMP)Wtsi)
|
cellular phenotype
|
J:333699
|
Nudctm1c(KOMP)Mbp/Nudctm1c(KOMP)Mbp Tg(Rho-icre)1Ck/0
(involves: C57BL/6 * C57BL/6N * SJL)
|
increased retina apoptosis
|
J:346299
|
Nudt1tm1Tts/Nudt1tm1Tts
(B6.129S-Nudt1tm1Tts)
|
abnormal cell physiology
|
J:79732
|
Nudt1tm1Tts/Nudt1tm1Tts Ogg1tm1Yun/Ogg1tm1Yun
(involves: 129S/SvEv * C57BL/6JJcl)
|
abnormal single-strand DNA break repair
|
J:193978
|
increased susceptibility to neuronal excitotoxicity
|
J:193978
|
Nudt2tm1a(EUCOMM)Wtsi/Nudt2tm1a(EUCOMM)Wtsi
(C57BL/6-Nudt2tm1a(EUCOMM)Wtsi)
|
abnormal fibroblast physiology
|
J:315167
|
Nudt7em1Ejj/Nudt7em1Ejj
(involves: C57BL/6N)
|
abnormal peroxisome physiology
|
J:266261
|
decreased chondrocyte proliferation
|
J:266261
|
increased chondrocyte apoptosis
|
J:266261
|
Numa1tm1.1Dwc/Numa1tm1.1Dwc Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL)
|
abnormal mitotic spindle morphology
|
J:146214
|
absent fibroblast proliferation
|
J:146214
|
cellular phenotype
|
J:146214
|
Numbtm1.1Ynj/Numbtm1.1Ynj
(involves: 129X1/SvJ * FVB/N)
|
abnormal neuron differentiation
|
J:62712
|
Numbtm1.1Zili/Numbtm1.1Zili
(involves: 129/Sv * FVB/N)
|
abnormal neuron differentiation
|
J:68652
|
abnormal vascular regression
|
J:68652
|
Numbtm1Ynj/Numbtm1Ynj Numbltm1Wmz/Numbltm1Wmz Tg(Nes-cre/Esr1*)4Ynj/0
(involves: 129X1/SvJ * C57BL/6)
|
increased neuron apoptosis
|
J:127227
|
Nup35m1Apb/Nup35m1Apb
(involves: C57BL/6N)
|
increased colon goblet cell number
|
J:235141
|
Nup88em1Jvd/Nup88+ Nup98tm1Jvd/Nup98+ Rae1tm1Jvd/Rae1+
(involves: C57BL/6)
|
abnormal mitosis
|
J:231166
|
Nup98tm1Bmaf/Nup98+
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased T cell proliferation
|
J:110907
|
increased T cell proliferation
|
J:110907
|
Nup98tm1Jvd/Nup98+ Rae1tm1Jvd/Rae1+
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:231166
|
abnormal mitosis
|
J:231166
|
abnormal mitotic spindle morphology
|
J:231166
|
Nup160tm1Mdan/Nup160tm1Mdan Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6)
|
decreased hematopoietic stem cell proliferation
|
J:301567
|
Nup210lTg(Gt(ROSA)26Sor-EGFP)130910Eps/Nup210lTg(Gt(ROSA)26Sor-EGFP)130910Eps
(FVB/NTac-Nup210lTg(Gt(ROSA)26Sor-EGFP)130910Eps/Mmmh)
|
abnormal acrosome morphology
|
J:171266
|
abnormal sperm midpiece morphology
|
J:171266
|
asthenozoospermia
|
J:171266
|
azoospermia
|
J:171266
|
decreased male germ cell number
|
J:171266
|
teratozoospermia
|
J:171266
|
Nup214tm1Gcg/Nup214tm1Gcg
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:36515
|
Nupr1tm1Jlio/Nupr1tm1Jlio
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell cycle
|
J:133728
|
abnormal cell death
|
J:133728
|
azoospermia
|
J:140899
|
increased fibroblast proliferation
|
J:133728
|
Nus1tm1Wcsa/Nus1tm1.1Wcsa
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
abnormal cell physiology
|
J:215785
|
abnormal cellular cholesterol metabolism
|
J:215785
|
increased sensitivity to induced cell death
|
J:215785
|
Nus1tm1Wcsa/Nus1tm1Wcsa
(Not Specified)
|
decreased lung endothelial cell proliferation
|
J:230506
|
increased lung endothelial cell apoptosis
|
J:230506
|
Nus1tm1Wcsa/Nus1tm1Wcsa Tg(Cdh5-cre/ERT2)1Rha/0
(Not Specified)
|
decreased endothelial cell proliferation
|
J:230506
|
increased vascular endothelial cell apoptosis
|
J:230506
|
Nusap1tm1.1Gcm/Nusap1tm1.1Gcm
(involves: 129/Sv * Swiss)
|
abnormal inner cell mass apoptosis
|
J:164315
|
abnormal mitosis
|
J:164315
|
abnormal mitotic spindle morphology
|
J:164315
|
increased mitotic index
|
J:164315
|
Nutm1tm1Ger/Nutm1tm1Ger
(involves: 129S2/SvPasCrl * C57BL/6)
|
azoospermia
|
J:271542
|
Nxf2tm1.1JwNxf3tm1.1Jw/Y Tg(Ddx4-cre)1Dcas/0
(involves: 129S4/SvJae * C57BL/6 * FVB)
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:199138
|
arrest of male meiosis
|
J:199138
|
elongated sperm flagellum
|
J:199138
|
globozoospermia
|
J:199138
|
oligozoospermia
|
J:199138
|
Nxf2tm1.2Jw/Y
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:149228
|
abnormal male meiosis
|
J:149228
|
arrest of male meiosis
|
J:149228
|
meiotic nondisjunction during M1 phase
|
J:149228
|
Nxf2tm1.2Jw/Y
(B6.Cg-Nxf2tm1.2Jw)
|
abnormal spermatogonia proliferation
|
J:149228
|
asthenozoospermia
|
J:149228
|
decreased male germ cell number
|
J:149228
|
decreased spermatogonia number
|
J:149228
|
oligozoospermia
|
J:149228
|
Nxf2tm1.2JwNxf3tm1.2Jw/Y
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
oligozoospermia
|
J:171521
|
Nxntm1Hmik/Nxntm1Hmik
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:167570
|
Oas1dtm1Zuk/Oas1dtm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
maternal effect
|
J:99134
|
Oas2M1Apb/Oas2M1Apb
(involves: C57BL/6J * CBA/CaJ)
|
decreased mammary gland epithelial cell proliferation
|
J:248944
|
increased apoptosis
|
J:248944
|
Oaz3tm1Htan/Oaz3tm1Htan
(involves: 129S1/Sv * C57BL/6)
|
detached sperm flagellum
|
J:161751
|
Obscntm1Chen/Obscntm1Chen Obsl1tm1.1Slan/Obsl1tm1.1Slan Tg(Myog-cre)1Eno/0
(involves: 129 * Black Swiss * C57BL/6 * SJL)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:283623
|
Oca2p-6H/Oca2p-6H
(involves: 101/H * C3H/HeH)
|
abnormal acrosome morphology
|
J:5219
|
abnormal gametes
|
J:5219
|
abnormal oogenesis
|
J:49046
|
abnormal sperm flagellum morphology
|
J:5219
|
abnormal sperm head morphology
|
J:5219
|
abnormal spermatid morphology
|
J:5219
|
decreased male germ cell number
|
J:5219
|
enlarged sperm head
|
J:5219
|
multinucleated giant male germ cells
|
J:49046
|
Oca2p-25H/Oca2p-25H
(Not Specified)
|
abnormal acrosome morphology
|
J:5219
|
abnormal sperm flagellum morphology
|
J:5219
|
abnormal sperm head morphology
|
J:5219
|
abnormal spermatid morphology
|
J:5219
|
decreased male germ cell number
|
J:5219
|
enlarged sperm head
|
J:5219
|
multinucleated giant male germ cells
|
J:5219
|
Oca2p-s/Oca2p-s
(Not Specified)
|
teratozoospermia
|
J:12939
|
Ociad1tm1.1Msin/Ociad1tm1.1Msin
(involves: BALB/cJ * C57BL/6NCrlj * CBA/JNCrlj)
|
decreased apoptosis
|
J:279239
|
increased hematopoietic stem cell proliferation
|
J:279239
|
Odad2b2b227.1Clo/Odad2b2b227.1Clo
(C57BL/6J-Odad2b2b227.1Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
immotile respiratory cilia
|
J:175213
|
Odad2b2b643Clo/Odad2b2b643Clo
(C57BL/6J-Odad2b2b643Clo)
|
abnormal respiratory motile cilium morphology
|
J:206685
|
abnormal respiratory motile cilium physiology
|
J:175213,
J:206685
|
immotile respiratory cilia
|
J:206685
|
Odad3b2b1885Clo/Odad3b2b1885Clo
(C57BL/6J-Odad3b2b1885Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
immotile respiratory cilia
|
J:175213
|
Odad3tm1b(EUCOMM)Hmgu/Odad3tm1b(EUCOMM)Hmgu
(C57BL/6N-Odad3tm1b(EUCOMM)Hmgu/Cnrm)
|
azoospermia
|
J:278798
|
Odad3tm1c(EUCOMM)Hmgu/Odad3tm1c(EUCOMM)Hmgu Gt(ROSA)26Sortm2(cre/ERT2)Brn/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N)
|
asthenozoospermia
|
J:278798
|
oligozoospermia
|
J:278798
|
Odad4em#Omra/Odad4em#Omra
(involves: C57BL/6)
|
absent nodal flow
|
J:244361
|
Odc1tm1Jlc/Odc1tm1Jlc
(involves: 129S1/Sv)
|
abnormal inner cell mass apoptosis
|
J:71462
|
Odf1tm1Shf/Odf1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
asthenozoospermia
|
J:183675
|
Odf1tm1Shf/Odf1tm1Shf
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal sperm midpiece morphology
|
J:183675
|
abnormal sperm mitochondrial sheath morphology
|
J:183675
|
asthenozoospermia
|
J:183675
|
coiled sperm flagellum
|
J:183675
|
detached sperm flagellum
|
J:183675
|
oligozoospermia
|
J:183675
|
Odf2Gt(XL169)Byg/Odf2+
(chimera involves: 129P2/OlaHsd * C57BL/6)
|
abnormal outer dense fiber morphology
|
J:163862
|
abnormal sperm axoneme morphology
|
J:163862
|
abnormal sperm flagellum morphology
|
J:163862
|
abnormal sperm midpiece morphology
|
J:163862
|
asthenozoospermia
|
J:163862
|
kinked sperm flagellum
|
J:163862
|
Odf2tm1.1Sats/Odf2tm1.2Sats Tg(CAG-cre)13Miya/0
(involves: C57BL/6 * C57BL/6J)
|
abnormal brain ependyma motile cilium morphology
|
J:181294
|
abnormal cilium morphology
|
J:181294
|
abnormal oviduct epithelium motile cilium morphology
|
J:181294
|
abnormal respiratory motile cilium morphology
|
J:181294
|
abnormal respiratory motile cilium physiology
|
J:181294
|
cellular phenotype
|
J:181294
|
decreased brain ependyma motile cilium number
|
J:181294
|
decreased embryonic cilium length
|
J:181294
|
decreased respiratory motile cilia number
|
J:181294
|
Odf4em1Ktos/Odf4em1Ktos
(involves: C57BL/6J * DBA/2J)
|
abnormal sperm flagellum morphology
|
J:333391
|
asthenozoospermia
|
J:333391
|
hairpin sperm flagellum
|
J:333391
|
oligozoospermia
|
J:333391
|
Ofd1tm2.1Bfra/Y Tg(CAG-cre)1Nagy/0
(involves: 129S2/SvPas)
|
abnormal neuron differentiation
|
J:106035
|
OgaGt(YTC085)Byg/OgaGt(YTC085)Byg
(B6J.129P2-OgaGt(YTC085)Byg)
|
abnormal mitosis
|
J:218150
|
abnormal mitotic cytokinesis
|
J:218150
|
aneuploidy
|
J:218150
|
chromosomal instability
|
J:218150
|
decreased fibroblast proliferation
|
J:218150
|
early cellular replicative senescence
|
J:218150
|
Ogg1tm1Tno/Ogg1tm1Tno
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal DNA repair
|
J:61684,
J:84649
|
Ogg1tm1Tno/Ogg1tm1Tno Tg(gptdelta)1Nmi/0
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell physiology
|
J:61684,
J:84649
|
Ogg1tm1Yun/Ogg1tm1Yun
(involves: 129S/SvEv * C57BL/6JJcl)
|
increased susceptibility to neuronal excitotoxicity
|
J:193978
|
Ogttm1Gwh/Y
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell death
|
J:93112,
J:62279
|
decreased cell proliferation
|
J:93112
|
Ogttm1Gwh/Y Tg(Lck-cre)548Jxm/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
increased T cell apoptosis
|
J:93112
|
Olig1tm1And/Olig1tm1And Olig2tm1And/Olig2tm1And
(involves: 129 * C57BL/6J)
|
decreased oligodendrocyte progenitor number
|
J:76446
|
Olig2tm1(cre/Esr1*)Htak/Olig2tm1(cre/Esr1*)Htak
(involves: BALB/c * C57BL/6 * C57BL/6NCrj * CBA)
|
abnormal neuronal migration
|
J:77821
|
decreased oligodendrocyte progenitor number
|
J:77821
|
Olig2tm1(cre/Esr1*)Htak/Olig2tm1(cre/Esr1*)Htak
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal cell differentiation
|
J:203419
|
Olig2tm1Rth/Olig2tm1Rth
(involves: 129S4/SvJae * C57BL/6J)
|
decreased oligodendrocyte progenitor number
|
J:75868
|
Olig3tm1Qiu/Olig3tm1Qiu
(Not Specified)
|
abnormal neuron differentiation
|
J:143462
|
Olig3tm1Tre/Olig3tm1Tre
(involves: 129P2/OlaHsd)
|
abnormal neuron differentiation
|
J:96749
|
abnormal neuronal migration
|
J:96749
|
Olig3tm1Tre/Olig3tm2(cre/ERT2)Cbm
(Not Specified)
|
abnormal neuron differentiation
|
J:143526
|
olt/olt
(involves: C3H/HeJOrl)
|
abnormal spermatid morphology
|
J:12215
|
azoospermia
|
J:24774
|
decreased spermatid number
|
J:12215
|
Om/Om+
(either: (DDK x C57BL/6J)F1 or (DDK x KK)F1 or (DDK x NC)F1)
|
abnormal female meiosis
|
J:98846
|
maternal effect
|
J:5498
|
Oma1tm1Otin/Oma1tm1Otin
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr)
|
abnormal cell physiology
|
J:184716
|
abnormal fat cell mitochondrial morphology
|
J:184716
|
abnormal mitochondrial morphology
|
J:184716
|
decreased cellular sensitivity to alkylating agents
|
J:184716
|
decreased fatty acid beta-oxidation
|
J:184716
|
decreased mitochondrial DNA content
|
J:184716
|
increased mitochondrial size
|
J:184716
|
Omptm4(cre)Mom/Omp+ Ric8btm1c(EUCOMM)Hmgu/Ric8btm1c(EUCOMM)Hmgu
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * SJL)
|
increased neuron apoptosis
|
J:247954
|
Onecut1tm1.1Mga/Onecut1tm1.1Mga Tg(Pdx1-cre)89.1Dam/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL)
|
abnormal pancreatic primary cilium morphology
|
J:155058
|
decreased pancreatic primary cilium number
|
J:155058
|
OoepGt(139A2)Cmhd/OoepGt(139A2)Cmhd
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal microtubule cytoskeleton morphology
|
J:276268
|
maternal effect
|
J:140105
|
Ooeptm1Miya/Ooeptm1Miya
(involves: 129P2/OlaHsd * C57BL/6J)
|
maternal effect
|
J:169631
|
Opa1lilr3/Opa1lilr3
(involves: C3H/HeJ * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:162916
|
Opa1Q285X/Opa1+
(involves: C3HeB/FeJ * C57BL/6JCrl)
|
abnormal mitochondrial morphology
|
J:121779
|
Opa1tm1.1Geno/Opa1+
(involves: 129S2/SvPas)
|
abnormal autophagy
|
J:237963
|
abnormal mitochondrial morphology
|
J:237963
|
abnormal mitochondrial physiology
|
J:237963
|
abnormal mitochondrial shape
|
J:237963
|
abnormal mitophagy
|
J:237963
|
decreased mitochondrial number
|
J:237963
|
decreased muscle fiber mitochondrial DNA content
|
J:237963
|
disorganized mitochondrial cristae
|
J:237963
|
increased mitochondrial number
|
J:237963
|
increased mitochondrial size
|
J:237963
|
Opa1tm1.1Hise/Opa1tm1.2Hise Tg(Ins2-cre)25Mgn/0
(involves: 129S/SvEv * C57BL/6 * DBA * SJL)
|
abnormal mitochondrial crista morphology
|
J:183074
|
abnormal mitochondrial morphology
|
J:183074
|
abnormal respiratory electron transport chain
|
J:183074
|
decreased pancreatic beta cell proliferation
|
J:183074
|
Opa1tm1Lsc/Opa1tm1Lsc
(involves: C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:214492
|
abnormal mitochondrial physiology
|
J:214492
|
Opa3m1Votr/Opa3m1Votr
(involves: C3H * C57BL/6JCrl)
|
abnormal mitochondrial morphology
|
J:181670
|
abnormal mitochondrial physiology
|
J:188346,
J:181670
|
cardiac interstitial fibrosis
|
J:181670
|
Ophn1Wtgr/Y
(D2(B6)-Ophn1Wtgr/EiGrsrJ)
|
asthenozoospermia
|
J:123336
|
Oprm1tm1Lyu/Oprm1+
(involves: Black Swiss)
|
increased splenocyte proliferation
|
J:39864
|
Oprm1tm1Lyu/Oprm1tm1Lyu
(involves: Black Swiss)
|
asthenozoospermia
|
J:39864
|
increased splenocyte proliferation
|
J:39864
|
oligozoospermia
|
J:39864
|
Optnem1Hyua/Optnem1Hyua
(C57BL/6J-Optnem1Hyua)
|
impaired autophagy
|
J:303304
|
increased retina apoptosis
|
J:303304
|
Or4m1em1Tshu/Or4m1em1Tshu
(involves: C57BL/6J)
|
asthenozoospermia
|
J:314392
|
decreased sperm progressive motility
|
J:314392
|
Or8a1tm16(Or8a1b/Or1f19)Mom/Or8a1tm16(Or8a1b/Or1f19)Mom
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal axon extension
|
J:91160
|
Or8a1tm17Mom/Or8a1tm17Mom
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal axon extension
|
J:91160
|
Or8a1tm20Mom/Or8a1tm20Mom
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal axon extension
|
J:91160
|
Or8a1tm21Mom/Or8a1tm21Mom
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal axon extension
|
J:91160
|
Or8a1btm4Mom/Or8a1b+ Ttc8tm1Reed/Ttc8tm1Reed
(involves: 129 * 129P2/OlaHsd * C57BL/6)
|
abnormal axon fasciculation
|
J:173465
|
abnormal axon guidance
|
J:173465
|
Or10a4tm1Mom/Or10a4+ Ttc8tm1Reed/Ttc8tm1Reed
(involves: 129 * 129P2/OlaHsd * C57BL/6)
|
abnormal axon guidance
|
J:173465
|
Orai1Gt(XL922)Byg/Orai1Gt(XL922)Byg
(involves: 129P2/OlaHsd * ICR)
|
abnormal Golgi apparatus morphology
|
J:315408
|
abnormal male germ cell physiology
|
J:315408
|
abnormal sperm head morphology
|
J:315408
|
abnormal spermatid morphology
|
J:315408
|
abnormal spermatocyte morphology
|
J:315408
|
asthenozoospermia
|
J:315408
|
decreased elongated spermatid number
|
J:315408
|
decreased sperm progressive motility
|
J:315408
|
dilated mitochondrion
|
J:315408
|
multinucleated giant male germ cells
|
J:315408
|
oligozoospermia
|
J:315408
|
Orai1tm1Rao/Orai1tm1Rao
(C57BL/6-Orai1tm1Rao)
|
abnormal cell physiology
|
J:139730
|
Orai2tm1.2Itl/Orai2tm1.2Itl
(involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6 * C57BL/6N)
|
increased mast cell degranulation
|
J:278536
|
Orc1tm1.1Gle/Orc1tm1.1Gle
(involves: C57BL/6 * SJL)
|
absent fibroblast proliferation
|
J:272584
|
decreased DNA replication
|
J:272584
|
polyploidy
|
J:272584
|
Orc1tm1.1Gle/Orc1tm1.1Gle Albtm1(cre/ERT2)Mtz/Alb+
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
cellular phenotype
|
J:272584
|
increased hepatocyte karyomegaly
|
J:272584
|
polyploidy
|
J:272584
|
Orc1tm1.1Gle/Orc1tm1.1Gle Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA * SJL)
|
abnormal DNA replication
|
J:272584
|
increased hepatocyte karyomegaly
|
J:272584
|
increased hepatocyte proliferation
|
J:272584
|
polyploidy
|
J:272584
|
Orc1tm1.1Gle/Orc1tm1.1Gle Tg(Cyp1a1-cre)1Dwi/0
(involves: C57BL/6 * CBA * SJL)
|
abnormal small intestinal crypt cell proliferation
|
J:272584
|
increased DNA replication
|
J:272584
|
increased small intestinal crypt cell apoptosis
|
J:272584
|
Orc1tm1.1Gle/Orc1tm1.2Gle Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA * SJL)
|
abnormal DNA replication
|
J:272584
|
increased hepatocyte karyomegaly
|
J:272584
|
polyploidy
|
J:272584
|
Orc3tm1.1Zhua/Orc3tm1.1Zhua Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas)
|
abnormal radial glial cell morphology
|
J:170581
|
decreased neuronal precursor proliferation
|
J:170581
|
decreased radial glial cell number
|
J:170581
|
Orc4tm1c(EUCOMM)Wtsi/Orc4tm1c(EUCOMM)Wtsi Tmem163Tg(ACTB-cre)2Mrt/Tmem163+
(involves: C57BL/6N * FVB/N)
|
abnormal female meiosis
|
J:326522
|
abnormal oocyte morphology
|
J:326522
|
abnormal polar body morphology
|
J:326522
|
Ormdl2em1Pdra/Ormdl2em1Pdra Ormdl3em1Pdra/Ormdl3em1Pdra
(C57BL/6-Ormdl2em1Pdra Ormdl3em1Pdra)
|
increased mast cell degranulation
|
J:328837
|
Ormdl3em1Pdra/Ormdl3em1Pdra
(C57BL/6-Ormdl3em1Pdra)
|
increased mast cell degranulation
|
J:328837
|
Os/Os
(involves: 101 * C3H)
|
abnormal mitosis
|
J:5768
|
increased mitotic index
|
J:5768
|
Osbp2tm1Arai/Osbp2tm1Arai
(C57BL/6-Osbp2tm1Arai)
|
abnormal acrosome morphology
|
J:215726
|
abnormal male germ cell apoptosis
|
J:215726
|
abnormal sperm head morphology
|
J:215726
|
abnormal sperm mitochondrial sheath morphology
|
J:215726
|
abnormal spermatid morphology
|
J:215726
|
absent sperm mitochondrial sheath
|
J:215726
|
asthenozoospermia
|
J:215726
|
globozoospermia
|
J:215726
|
oligozoospermia
|
J:215726
|
teratozoospermia
|
J:215726
|
Osbpl2em1Cya/Osbpl2em1Cya
(C57BL/6-Osbpl2em1Cya)
|
abnormal inner hair cell kinocilium morphology
|
J:324115
|
abnormal outer hair cell kinocilium morphology
|
J:324115
|
abnormal primary cilium morphology
|
J:324115
|
Oscartm1Ywc/Oscartm1Ywc
(involves: 129P2/OlaHsd)
|
abnormal osteoclast differentiation
|
J:178250
|
Oscartm1Ywc/Oscartm1Ywc Tyrobptm1Ttk/Tyrobptm1Ttk
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:178250
|
Osr1tm1Jian/Osr1tm1Jian
(either: (involves: 129S1/Sv * C57BL/6J) or (involves: 129S1/Sv * ICR))
|
increased kidney apoptosis
|
J:104942
|
Osr1tm1Jian/Osr1tm1Jian
(involves: 129S1/Sv)
|
increased metanephric mesenchyme apoptosis
|
J:117734
|
Ostntm1.1Geno/Ostntm1.1Geno
(involves: C57BL/6)
|
decreased mitochondrial size
|
J:228285
|
Otcspf-ash/Y
(Not Specified)
|
abnormal mitochondrial physiology
|
J:26976
|
Otud7btm1Dgen/Otud7btm1Dgen
(involves: 129 * C57BL/6)
|
decreased activation-induced B cell apoptosis
|
J:194553
|
increased B cell proliferation
|
J:194553
|
Otulinm3Sapc/Otulinm3Sapc
(C57BL/6J-Otulinm3Sapc)
|
abnormal vascular endothelial cell migration
|
J:197674
|
Otulintm1c(EUCOMM)Hmgu/Otulintm1c(EUCOMM)Hmgu Tg(KRT14-cre)1Cgn/0
(involves: C57BL/6 * C57BL/6N * DBA/2)
|
abnormal epidermal stem cell apoptosis
|
J:312394
|
abnormal epidermal stem cell proliferation
|
J:312394
|
abnormal keratinocyte differentiation
|
J:312394
|
Otx1tm4(cre)Asim/Otx1+ Otx2tm6Asim/Otx2tm6.1Asim
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal neuronal precursor proliferation
|
J:83110
|
Otx2tm6Asim/Otx2tm11Asim Slc6a3tm1.1(cre)Bkmn/Slc6a3+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:166896
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:166896
|
Ovch2em1Osb/Ovch2em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
impaired sperm migration in female genital tract
|
J:290452
|
Ovol1tm1Efu/Ovol1tm1Efu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased male germ cell number
|
J:50844
|
Ovol2tm1Xdai/Ovol2tm1Xdai
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1))
|
abnormal neural crest cell delamination
|
J:106405
|
increased neural crest cell apoptosis
|
J:106405
|
Oxct1tm1a(KOMP)Wtsi/Oxct1tm1a(KOMP)Wtsi
(C57BL/6-Oxct1tm1a(KOMP)Wtsi)
|
abnormal autophagy
|
J:170537
|
Oxr1tm1a(EUCOMM)Wtsi/Oxr1tm1a(EUCOMM)Wtsi
(C57BL/6N-Oxr1tm1a(EUCOMM)Wtsi)
|
increased neuron apoptosis
|
J:230923
|
P2rx1tm1Chn/P2rx1tm1Chn
(involves: 129P2/OlaHsd * MF1)
|
azoospermia
|
J:59336
|
P2rx2em1Xzl/P2rx2+
(CBA/J-P2rx2em1Xzl)
|
cellular phenotype
|
J:315007
|
decreased dermal fibroblast proliferation
|
J:315007
|
P2rx7rs48804829-T/P2rx7rs48804829-T
(C57BL/6)
|
abnormal apoptosis
|
J:89513
|
abnormal cell death
|
J:89513
|
P2rx7tm1.1(P2RX7)Jde/P2rx7tm2.1(P2RX7*)Jde
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal cell physiology
|
J:251657
|
P2rx7tm1Gab/P2rx7tm1Gab
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * DBA/2))
|
abnormal cell death
|
J:89513
|
P2ry2tm1Bhk/P2ry2tm1Bhk
(involves: 129P2/OlaHsd)
|
abnormal axon extension
|
J:104694
|
abnormal neuron differentiation
|
J:104694
|
P2ry6tm1Jabo/P2ry6tm1Jabo Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: 129 * C57BL/6 * C57BL/6NTac)
|
decreased T cell apoptosis
|
J:179177
|
increased T cell proliferation
|
J:179177
|
P2ry13tm1Loma/P2ry13tm1Loma
(B6.129-P2ry13tm1Loma)
|
abnormal cellular cholesterol metabolism
|
J:166205
|
P4ha1tm1Jomy/P4ha1tm1Jomy
(involves: 129/Sv * C57BL)
|
abnormal endoplasmic reticulum morphology
|
J:120302
|
impaired basement membrane formation
|
J:120302
|
Pa2g4Gt(OST186047)Lex/Pa2g4Gt(OST186047)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
decreased cell proliferation
|
J:151280
|
early cellular replicative senescence
|
J:151280
|
Pabpc1ltm1.1Esel/Pabpc1ltm1.1Esel
(involves: 129S1/SvImJ * C57BL/6J)
|
abnormal cell physiology
|
J:187525
|
abnormal oocyte morphology
|
J:187525
|
abnormal oogenesis
|
J:187525
|
abnormal spindle assembly in female meiosis
|
J:187525
|
decreased oocyte number
|
J:187525
|
Pabpn1tm1.2Gpvl/Pabpn1+
(involves: C57BL/6 * FVB/N)
|
abnormal mitochondrial physiology
|
J:243638
|
abnormal oxidative phosphorylation
|
J:243638
|
Pabpn1tm2.2Gpvl/Pabpn1+
(involves: C57BL/6 * FVB/N)
|
abnormal mitochondrial physiology
|
J:243638
|
abnormal oxidative phosphorylation
|
J:243638
|
Pabpn1lem1Hyfn/Pabpn1lem1Hyfn
(C57BL/6-Pabpn1lem1Hyfn)
|
abnormal oocyte morphology
|
J:302699
|
maternal effect
|
J:302699
|
Pacc1em1.1Zzq/Pacc1em1.1Zzq
(involves: C57BL/6 * FVB/N)
|
decreased sensitivity to induced cell death
|
J:273611
|
Pacs2Gt(OST426086)Lex/Pacs2Gt(OST426086)Lex
(involves: 129S5/SvEvBrd * NIH Black Swiss)
|
decreased apoptosis
|
J:136536
|
Pacsin1tm1.1Bqu/Pacsin1tm1.1Bqu
(Not Specified)
|
abnormal vesicle-mediated transport
|
J:180017
|
Padi4tm1.1Ywan/Padi4tm1.1Ywan
(involves: 129S4/SvJae)
|
impaired neutrophil phagocytosis
|
J:165718
|
Padi6tm1.1Jgo/Padi6tm1.1Jgo
(involves: BALB/cJ)
|
abnormal oocyte morphology
|
J:138684
|
Padi6tm1.1Jgo/Padi6tm1.1Jgo
(Not Specified)
|
abnormal oocyte morphology
|
J:138573
|
Paf/Y
(involves: C3H/HeSn)
|
abnormal meiosis
|
J:10459
|
meiotic nondisjunction during M1 phase
|
J:10459
|
Paf/Y
(C3H/HeSn-Paf/J)
|
abnormal meiosis
|
J:137513
|
meiotic nondisjunction during M1 phase
|
J:137513
|
Pafah1b1Gt(IRESBetageo)1Hha/Pafah1b1Gt(IRESBetageo)1Hha
(involves: 129/Sv * NMRI)
|
abnormal acrosome morphology
|
J:86720
|
abnormal germ cell morphology
|
J:86720
|
abnormal spermatid morphology
|
J:86720
|
abnormal spermatogonia morphology
|
J:86720
|
azoospermia
|
J:86720
|
Pafah1b1tm1Awb/Pafah1b1+
(involves: 129S6/SvEvTac)
|
abnormal neuronal migration
|
J:100552
|
increased neuron apoptosis
|
J:100552
|
Pafah1b1tm1Awb/Pafah1b1+ Ndel1tm1.1Shr/Ndel1+
(involves: 129S6/SvEvTac)
|
abnormal neuronal migration
|
J:100552
|
increased neuron apoptosis
|
J:100552
|
Pafah1b1tm1Awb/Pafah1b1+ Pafah1b2Gt(Betageo)1Cla/Pafah1b2Gt(Betageo)1Cla Pafah1b3tm1Cla/Pafah1b3tm1Cla
(involves: 129S6/SvEvTac)
|
decreased male germ cell number
|
J:83818
|
multinucleated giant male germ cells
|
J:83818
|
Pafah1b1tm1Awb/Pafah1b1+ Ywhaetm1Awb/Ywhae+
(either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss))
|
decreased neuronal migration
|
J:84075
|
Pafah1b1tm1Or/Pafah1b1+
(Not Specified)
|
abnormal radial glial cell morphology
|
J:69631
|
Pafah1b2Gt(Betageo)1Cla/Pafah1b2Gt(Betageo)1Cla
(involves: 129S6/SvEvTac)
|
abnormal spermatid morphology
|
J:83818
|
abnormal spermatocyte morphology
|
J:83818
|
decreased male germ cell number
|
J:83818
|
multinucleated giant male germ cells
|
J:83818
|
Pafah1b2Gt(Betageo)1Cla/Pafah1b2Gt(Betageo)1Cla Pafah1b3tm1Cla/Pafah1b3tm1Cla
(involves: 129S6/SvEvTac)
|
decreased male germ cell number
|
J:83818
|
multinucleated giant male germ cells
|
J:83818
|
Pafah1b2tm1Arai/Pafah1b2tm1Arai Pafah1b3tm1Arai/Pafah1b3tm1Arai
(involves: 129X1/SvJ * C57BL/6N)
|
abnormal male germ cell morphology
|
J:82792
|
abnormal spermatid morphology
|
J:82792
|
azoospermia
|
J:82792
|
decreased male germ cell number
|
J:82792
|
increased male germ cell apoptosis
|
J:82792
|
Pafah2tm1Arai/Pafah2tm1Arai
(B6.129P2-Pafah2tm1Arai)
|
increased cellular sensitivity to oxidative stress
|
J:130728
|
Pagr1atm1Kaig/Pagr1atm1Kaig
(involves: 129S6/SvEvTac * C57BL/6)
|
increased allantois apoptosis
|
J:210984
|
increased embryonic neuroepithelium apoptosis
|
J:210984
|
Paip2tm1.2Nso/Paip2tm1.2Nso Paip2btm1.2Nso/Paip2btm1.2Nso
(B6.129-Paip2btm1.2Nso Paip2tm1.2Nso)
|
abnormal sperm nucleus morphology
|
J:165272
|
abnormal spermatid morphology
|
J:165272
|
absent sperm mitochondrial sheath
|
J:165272
|
azoospermia
|
J:165272
|
decreased male germ cell number
|
J:165272
|
detached acrosome
|
J:165272
|
teratozoospermia
|
J:165272
|
Pak1tm1.1Xwg/Pak1tm1.1Xwg Myl2tm1(cre)Krc/Myl2+
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:193804
|
Pak1tm1Cher/Pak1tm1Cher
(B6.129S2-Pak1tm1Cher)
|
decreased mast cell degranulation
|
J:145444
|
Pak1ip1mray/Pak1ip1mray
(involves: C57BL/6J * FVB/NJ)
|
decreased cell proliferation
|
J:204457
|
Pak2Gt(OST104058)Lex/Pak2+
(B6;129S5-Pak2Gt(OST104058)Lex/J)
|
abnormal actin cytoskeleton morphology
|
J:271067
|
abnormal neuronal migration
|
J:271067
|
Pak2tm1.1Rjak/Pak2tm1.1Rjak
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell death
|
J:171914
|
increased fibroblast proliferation
|
J:171914
|
Pak3tm1.1Rpo/Y
(B6.129S2(Cg)-Pak3tm1.1Rpo)
|
abnormal neuron differentiation
|
J:292116
|
Pak4tm1Amin/Pak4tm1Amin
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S2/SvPas * C57BL/6))
|
abnormal axon extension
|
J:85954
|
abnormal cell adhesion
|
J:85954
|
abnormal neuron differentiation
|
J:85954
|
abnormal neuronal migration
|
J:85954
|
Pak4tm1Amin/Pak4tm1Amin
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129S2/SvPas * C57BL/6J))
|
decreased cell proliferation
|
J:152821
|
increased apoptosis
|
J:152821
|
pal/pal
(involves: 129S1/Sv * C57BL/6 * FVB/NJ)
|
abnormal neuron differentiation
|
J:171522
|
Palb2Gt(CG0691)Wtsi/Palb2Gt(CG0691)Wtsi
(involves: 129P2/OlaHsd * C57BL/6N)
|
decreased inner cell mass proliferation
|
J:161528
|
Palb2tm1.1Dli/Palb2tm1.1Dli Trp53bp1tm1Jc/Trp53bp1tm1Jc Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6)
|
chromosome breakage
|
J:197442
|
Pald1tm1Vlcg/Pald1tm1Vlcg
(B6.Cg-Pald1tm1Vlcg)
|
increased lung endothelial cell apoptosis
|
J:254363
|
increased lung endothelial cell proliferation
|
J:254363
|
Palldtm1Zgwg/Palldtm1Zgwg
(involves: C57BL/6)
|
abnormal cell adhesion
|
J:100650
|
decreased fibroblast cell migration
|
J:100650
|
Pals1tm1Caw/Pals1+ Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas)
|
abnormal neuronal precursor proliferation
|
J:160624
|
premature neuronal precursor differentiation
|
J:160624
|
Pals1tm1Caw/Pals1tm1Caw Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas)
|
abnormal neuronal precursor proliferation
|
J:160624
|
increased neuron apoptosis
|
J:160624
|
premature neuronal precursor differentiation
|
J:160624
|
Pals1tm1Caw/Pals1tm1Caw Tg(rx3-icre)1Mjam/0
(Not Specified)
|
abnormal cell proliferation
|
J:184469
|
decreased cell proliferation
|
J:184469
|
increased retina apoptosis
|
J:184469
|
Pank1tm1.1Suja/Pank1tm1.1Suja
(involves: 129S/SvEv)
|
decreased fatty acid oxidation
|
J:189609
|
Pank1tm1.1Suja/Pank1tm1.1Suja Pank2tm1.1Suja/Pank2tm1.1Suja
(involves: 129S/SvEv * C57BL/6J * FVB/N)
|
decreased fatty acid oxidation
|
J:189609
|
Pank2tm1.1Suja/Pank2tm1.1Suja
(involves: 129S/SvEv * C57BL/6J * FVB/N)
|
azoospermia
|
J:189609
|
Pank2tm1Jgt/Pank2tm1Jgt
(involves: 129X1/SvJ * C57BL/6J)
|
azoospermia
|
J:94753
|
Pank4em1Nju/Pank4em1Nju
(Not Specified)
|
increased lens epithelium apoptosis
|
J:301838
|
Panx1tm1.1Vshe/Panx1tm1.1Vshe
(B6.129-Panx1tm1.1Vshe)
|
decreased neuron apoptosis
|
J:196355
|
Panx1tm1a(KOMP)Wtsi/Panx1tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal cell physiology
|
J:175396
|
Panx1tm1Vshe/Panx1tm1Vshe Tg(Thy1-cre)1Vln/0
(B6.Cg-Panx1tm1Vshe Tg(Thy1-cre)1Vln)
|
decreased neuron apoptosis
|
J:196355
|
Papolbtm1Tba/Papolbtm1Tba
(involves: 129S2/SvPas * C57BL/6)
|
increased male germ cell apoptosis
|
J:80657
|
Paqr3tm1Ychn/Paqr3tm1Ychn
(involves: 129 * C57BL/6J)
|
increased keratinocyte proliferation
|
J:139058
|
Pargtm1Tmd/Pargtm1Tmd
(involves: 129X1/SvJ)
|
decreased cell proliferation
|
J:95214
|
increased apoptosis
|
J:95214
|
Park7Gt(XE726)Byg/Park7Gt(XE726)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:134826
|
Park7Gt(XE726)Byg/Park7Gt(XE726)Byg Pink1tm1.1Wrst/Pink1tm1.1Wrst
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6J)
|
cellular phenotype
|
J:242309
|
Park7Gt(XE726)Byg/Park7Gt(XE726)Byg Pink1tm1.1Wrst/Pink1tm1.1Wrst Rrn3tm1.1Igt/Rrn3tm1.1Igt Tg(Slc6a3-cre/ERT2)1Span/0
(involves: 129 * 129P2/OlaHsd * 129S2/SvPas * C57BL/6J)
|
abnormal cell physiology
|
J:242309
|
abnormal nucleolus morphology
|
J:242309
|
Park7tm1Tmd/Park7tm1Tmd
(involves: 129S/SvEv * C57BL/6)
|
abnormal cellular respiration
|
J:125021
|
abnormal tricarboxylic acid cycle
|
J:125021
|
Parltm1.1Bdes/Parltm1.1Bdes
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:116017
|
abnormal mitochondrial physiology
|
J:116017
|
increased neuron apoptosis
|
J:116017
|
increased T cell apoptosis
|
J:116017
|
Parltm1.1Bdes/Parltm1.1Bdes
(involves: 129P2/OlaHsd)
|
abnormal mitochondrial crista morphology
|
J:269785
|
abnormal mitochondrial morphology
|
J:269785
|
abnormal mitochondrial physiology
|
J:269785
|
abnormal respiratory electron transport chain
|
J:269785
|
abnormal thymus apoptosis
|
J:269785
|
Parltm1Bdes/Parltm1Bdes Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal mitochondrial morphology
|
J:269785
|
abnormal thymus apoptosis
|
J:269785
|
Parp1tm1Jmdm/Parp1+ Parp2tm1Jmdm/Parp2tm1Jmdm
(involves: 129S2/SvPas * C57BL/6)
|
aneuploidy
|
J:83371
|
chromosomal instability
|
J:83371
|
Parp1tm1Jmdm/Parp1tm1Jmdm
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:41742
|
abnormal DNA repair
|
J:41742
|
abnormal leukocyte migration
|
J:117701
|
elevated level of mitotic sister chromatid exchange
|
J:41742
|
increased apoptosis
|
J:41742
|
induced chromosome breakage
|
J:41742
|
Parp1tm1Zqw/Parp1tm1Zqw
(involves: 129S2/SvPas * C57BL/6)
|
decreased cell proliferation
|
J:23942
|
decreased neuron apoptosis
|
J:65747
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:23942
|
Parp1tm1Zqw/Parp1tm1Zqw
(129S-Parp1tm1Zqw/J)
|
decreased neuron apoptosis
|
J:96548
|
decreased renal tubule apoptosis
|
J:95418
|
Parp2tm1Jmdm/Parp2tm1Jmdm
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:83371
|
abnormal DNA repair
|
J:83371
|
cellular phenotype
|
J:83371
|
elevated level of mitotic sister chromatid exchange
|
J:83371
|
increased cellular sensitivity to gamma-irradiation
|
J:83371
|
induced chromosome breakage
|
J:83371
|
Parp11tm1(KOMP)Vlcg/Parp11tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal sperm head morphology
|
J:221906
|
abnormal sperm nucleus morphology
|
J:221906
|
abnormal spermatid morphology
|
J:221906
|
teratozoospermia
|
J:221906
|
Parp14Gt(OST415485)Lex/Parp14Gt(OST415485)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
decreased B cell proliferation
|
J:146533
|
increased B cell apoptosis
|
J:146533
|
increased B cell proliferation
|
J:146533
|
increased cellular sensitivity to gamma-irradiation
|
J:146533
|
Pas17C57BL/6JBy/Pas17C57BL/6JBy Politm1.1Lgh/Politm1.1Lgh
(involves: C57BL/6J)
|
abnormal cell physiology
|
J:212610
|
Patl2tm1b(EUCOMM)Hmgu/Patl2tm1b(EUCOMM)Hmgu
(involves: C57BL/6N * FVB/N)
|
abnormal female meiosis
|
J:264835
|
abnormal female meiosis I arrest
|
J:264835
|
abnormal meiotic spindle morphology
|
J:264835
|
abnormal oocyte morphology
|
J:264835
|
abnormal oogenesis
|
J:264835
|
impaired spindle assembly in female meiosis
|
J:264835
|
Patz1tm1.2Welm/Patz1tm1.2Welm Commd10Tg(Vav1-icre)A2Kio/Commd10+
(B6.Cg-Patz1tm1.2Welm Commd10Tg(Vav1-icre)A2Kio)
|
abnormal mast cell differentiation
|
J:209168
|
Patz1tm1Pchi/Patz1+
(involves: C57BL/6J)
|
increased fibroblast proliferation
|
J:190572
|
Patz1tm1Pchi/Patz1tm1Pchi
(Not Specified)
|
abnormal spermatogonia proliferation
|
J:133515
|
azoospermia
|
J:133515
|
Patz1tm1Pchi/Patz1tm1Pchi
(involves: C57BL/6J)
|
abnormal cell cycle
|
J:190572
|
decreased fibroblast proliferation
|
J:190572
|
early cellular replicative senescence
|
J:190572
|
Pawrtm1Jmos/Pawrtm1Jmos
(involves: 129/Sv * CD-1)
|
decreased sensitivity to induced cell death
|
J:86034
|
increased B cell proliferation
|
J:85495
|
increased T cell proliferation
|
J:85495
|
Pax1tm2.1Tlu/Pax1tm2.1Tlu
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ)
|
decreased cell proliferation
|
J:198603
|
Pax21Neu/Pax2+
(involves: 102 * C57BL/6)
|
increased kidney apoptosis
|
J:59408,
J:86661
|
Pax21Neu/Pax2+
(involves: 102)
|
increased kidney apoptosis
|
J:136502
|
Pax21Neu/Pax2+ Wt1tm1Jae/Wt1+
(involves: 102 * 129S4/SvJae * C57BL/6)
|
increased kidney apoptosis
|
J:86661
|
Pax2tm1Pgr/Pax2tm1Pgr
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal axon extension
|
J:36834
|
Pax2tm2(Pax5)Mbu/Pax2tm2(Pax5)Mbu
(C3.129P2-Pax2tm2(Pax5)Mbu)
|
increased kidney apoptosis
|
J:63683
|
Pax3Sp-2H/Pax3Sp-2H
(involves: C57BL/6)
|
abnormal muscle precursor cell migration
|
J:32016
|
Pax3Sp-7H/Pax3Sp-7H
(involves: C3H/HeH * C57BL/6)
|
abnormal neural crest cell migration
|
J:93195
|
Pax3Sp/Pax3Sp
(C57BL-Pax3Sp)
|
increased mitotic index
|
J:13016
|
Pax3Sp/Pax3Sp
(involves: C57BL)
|
abnormal muscle precursor cell migration
|
J:32016
|
Pax3Sp/Pax3Sp
(involves: 129S2/SvPas * C57BL * C57BL/6J * FVB)
|
increased embryonic neuroepithelium apoptosis
|
J:75569
|
Pax3tm1(cre)Joe/Pax3+ Rbpjtm1Hon/Rbpjtm1Hon
(involves: 129P2/OlaHsd)
|
abnormal neuron differentiation
|
J:130251
|
Pax3tm1Buck/Pax3Sp
(involves: 129P2/OlaHsd * C57BL)
|
abnormal neural crest cell migration
|
J:86911
|
Pax3tm1Buck/Pax3tm1Buck
(involves: 129P2/OlaHsd)
|
abnormal muscle precursor cell migration
|
J:176192
|
abnormal neural crest cell migration
|
J:176192
|
Pax3tm3(Pax7)Buck/Pax3tm3(Pax7)Buck
(involves: 129S2/SvPas)
|
abnormal neural crest cell migration
|
J:90568
|
Pax3tm3.1(Pax7)Buck/Pax3Sp
(involves: 129S2/SvPas)
|
decreased cell proliferation
|
J:90568
|
Pax3tm3.1(Pax7)Buck/Pax3tm3.1(Pax7)Buck
(involves: 129S2/SvPas)
|
abnormal muscle precursor cell migration
|
J:90568
|
decreased cell proliferation
|
J:90568
|
Pax3tm6(Pax8)Buck/Pax3tm6(Pax8)Buck
(involves: 129S2/SvPas)
|
abnormal neural crest cell migration
|
J:176192
|
Pax3tm6.1(Pax8)Buck/Pax3tm6.1(Pax8)Buck
(involves: 129S2/SvPas * BALB/c * C57BL/6)
|
abnormal muscle precursor cell migration
|
J:176192
|
abnormal neural crest cell migration
|
J:176192
|
Pax5tm1Mbu/Pax5tm1Mbu
(involves: 129S2/SvPas)
|
abnormal cell adhesion
|
J:123629
|
enhanced B cell migration
|
J:123629
|
Pax6Mhdaaey18/Pax6Mhdaaey18
(involves: C3HeB/FeJ)
|
abnormal neuron differentiation
|
J:94457
|
Pax6Sey/Pax6Sey
(Not Specified)
|
abnormal neuron differentiation
|
J:112802
|
Pax6Sey/Pax6Sey
(involves: C57BL/6J * DBA/2J)
|
abnormal neuron differentiation
|
J:94457
|
Pax6tm1.1Zkoz/Pax6tm1.1Zkoz Tg(Rax-cre)1Zkoz/0
(Not Specified)
|
abnormal cell cycle
|
J:208421
|
abnormal cell cycle checkpoint function
|
J:208421
|
abnormal mitosis
|
J:208421
|
decreased cell proliferation
|
J:208421
|
increased retina apoptosis
|
J:208421
|
Pax6tm2(Pax6_i5a,Pax2)Xzh/Pax6tm2(Pax6_i5a,Pax2)Xzh
(involves: 129S6/SvEvTac)
|
abnormal neuronal precursor proliferation
|
J:198381
|
Pax6tm2.1(Pax6_i5a,Pax2)Xzh/Pax6tm2.1(Pax6_i5a,Pax2)Xzh
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N)
|
abnormal neuronal precursor proliferation
|
J:198381
|
Pax6tm2Pgr/Pax6tm2Pgr Sox2tm1.1Lan/Sox2tm1.1Lan Tg(Cryaa-cre)10Mlr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL)
|
increased lens epithelium apoptosis
|
J:152850
|
Pax6tm2Pgr/Pax6tm2Pgr Tg(Cryaa-cre)10Mlr/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
increased lens epithelium apoptosis
|
J:152850
|
Pax7tm1.1Thbr/Pax7tm1.1Thbr
(Not Specified)
|
abnormal skeletal muscle satellite cell proliferation
|
J:202693
|
Pax7tm1.1Thbr/Pax7tm2.1(cre/ERT2)Fan
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal skeletal muscle satellite cell proliferation
|
J:202693
|
Pax7tm1Pgr/Pax7tm1Pgr
(involves: 129S2/SvPas)
|
cellular phenotype
|
J:64793
|
Pax8tm1Pgr/Pax8tm1Pgr
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal kinocilium morphology
|
J:116236
|
Pax8tm1Rdl/Pax8tm1.1(cre)Mbu
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased apoptosis
|
J:178498
|
Pax8tm1Rdl/Pax8tm1.1(cre)Mbu
(B6.129(Cg)-Pax8tm1Rdl Pax8tm1.1(cre)Mbu)
|
increased apoptosis
|
J:220108
|
Paxip1tm1Gdr/Paxip1tm1Gdr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal DNA repair
|
J:82319
|
abnormal mitosis
|
J:82319
|
decreased cell proliferation
|
J:82319
|
decreased DNA replication
|
J:82319
|
decreased inner cell mass proliferation
|
J:82319
|
increased cellular sensitivity to ionizing radiation
|
J:82319
|
increased embryonic tissue cell apoptosis
|
J:82319
|
Paxxem1Spj/Paxxem1Spj
(C57BL/6NTac-Paxxem1Spj)
|
cellular phenotype
|
J:236776
|
Paxxem1Spj/Paxxem1Spj Nhej1tm1Fwa/Nhej1tm1Fwa
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
chromosomal instability
|
J:236776
|
increased neural tube apoptosis
|
J:236776
|
Pbrm1tm1Zhwa/Pbrm1tm1Zhwa Tg(Cd4-cre)1Cwi/?
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:236906
|
Pbx1tm1Koss/Pbx1tm1Koss Pbx2tm1Mlc/Pbx2tm1Mlc Foxg1tm1(cre)Skm/Foxg1+
(involves: 129P2/OlaHsd * 129S/Sv)
|
decreased apoptosis
|
J:178316
|
Pbx1tm1Mlc/Pbx1tm1Mlc
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased chondrocyte proliferation
|
J:71996
|
Pcaretm1Kpal/Pcaretm1Kpal
(involves: C57BL/6J * C57BL/6NTac)
|
abnormal photoreceptor connecting cilium morphology
|
J:220866
|
Pcbp4Gt(D136D11)Wrst/Pcbp4Gt(D136D11)Wrst
(involves: 129S2/SvPas * C57BL/6)
|
delayed cellular replicative senescence
|
J:231514
|
increased fibroblast proliferation
|
J:231514
|
Pccatm1Tmiy/Pccatm1Tmiy Tg(CAG-PCCA*A138T,-EGFP)#Miab/0
(involves: 129P2/OlaHsd * FVB/N)
|
maternal effect
|
J:286218
|
oxidative stress
|
J:282292
|
Pcdh15av-3J/Pcdh15av-3J
(C57BL/6J-Pcdh15av-3J/J)
|
abnormal inner hair cell kinocilium morphology
|
J:135991
|
abnormal outer hair cell kinocilium morphology
|
J:135991
|
Pcdh15av-5J/Pcdh15av-5J
(C57BL/6J-Pcdh15av-5J/J)
|
abnormal vestibular hair cell kinocilium morphology
|
J:112247
|
Pcdh15roda/Pcdh15roda
(BALB/c-Pcdh15roda)
|
abnormal inner hair cell kinocilium location or orientation
|
J:220658
|
Pcdh15tm2.1Mll/Pcdh15tm2.1Mll
(involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6 * SJL)
|
abnormal inner hair cell kinocilium location or orientation
|
J:171627
|
abnormal outer hair cell kinocilium location or orientation
|
J:171627
|
abnormal vestibular hair cell kinocilium morphology
|
J:171627
|
Pcdh19tm1Tac/Y
(involves: 129S/SvEv * C57BL/6)
|
abnormal neuronal migration
|
J:256961
|
Pcdh19tm1Tac/Pcdh19tm1Tac
(involves: 129S/SvEv * C57BL/6)
|
abnormal neuronal migration
|
J:256961
|
Pcdhgem5Rwb/Pcdhgem5Rwb
(C57BL/6J-Pcdhgem5Rwb/Rwb)
|
increased spinal cord apoptosis
|
J:285314
|
Pcdhgem41Rwb/Pcdhgem41Rwb
(C57BL/6J-Pcdhgem41Rwb/Rwb)
|
increased spinal cord apoptosis
|
J:285314
|
Pcdhgtm1.1Tman/Pcdhgtm1.1Tman
(involves: 129S4/SvJae * C57BL/6)
|
increased neuron apoptosis
|
J:188341
|
Pcdhgtm2Xzw/Pcdhgtm2Xzw Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
(involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL)
|
increased retina apoptosis
|
J:142186
|
Pcgf2tm1Hko/Pcgf2tm1Hko Bmi1tm1Brn/Bmi1tm1Brn
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased neural tube apoptosis
|
J:68216
|
Pclaftm1.1Lkd/Pclaftm1.1Lkd
(involves: C57BL/6)
|
oxidative stress
|
J:177782
|
Pcmt1tm1Scl/Pcmt1tm1Scl
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell physiology
|
J:40967
|
Pcmt1tm1Shs/Pcmt1tm1Shs
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:46228
|
Pcnatm1.1Mdsc/Pcnatm1.1Mdsc Tg(Pcna*K164R)1Mdsc/0
(involves: FVB/N)
|
abnormal meiosis
|
J:141098
|
Pcnatm1Jcbs/Pcnatm1Jcbs
(involves: 129P2/OlaHsd * C57BL/6)
|
absent germ cells
|
J:125916
|
PcntGt(RRU388)Byg/PcntGt(RRU388)Byg
(B6.129P2-PcntGt(RRU388)Byg)
|
abnormal mitotic spindle morphology
|
J:226309
|
abnormal neuron differentiation
|
J:226309
|
Pcsk1em2Irli/Pcsk1em2Irli
(C57BL/6J-Pcsk1em2Irli)
|
abnormal intestinal goblet cell morphology
|
J:324309
|
Pcsk2tm1Dfs/Pcsk2tm1Dfs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal pancreatic beta cell differentiation
|
J:85590
|
increased pancreatic alpha cell proliferation
|
J:85590
|
Pcsk2tm1Dfs/Pcsk2tm1Dfs
(B6;129-Pcsk2tm1Dfs/J)
|
abnormal pancreatic alpha cell differentiation
|
J:236905
|
Pcsk4tm1Mbi/Pcsk4tm1Mbi
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased hyperactivated sperm motility
|
J:41503
|
Pcsk4tm1Mbi/Pcsk4tm1Mbi
(B6.129P2-Pcsk4tm1Mbi)
|
abnormal acrosome assembly
|
J:233570
|
abnormal proacrosomal vesicle fusion
|
J:233570
|
abnormal sperm head morphology
|
J:233570
|
Pcsk5b2b1549Clo/Pcsk5b2b1549Clo
(C57BL/6J-Pcsk5b2b1549Clo)
|
abnormal respiratory motile cilium physiology
|
J:175213
|
immotile respiratory cilia
|
J:175213
|
Pcsk5vcc/Pcsk5vcc
(involves: C57BL/6J)
|
patent ductus arteriosus
|
J:136243
|
Pctptm1Bor/Pctptm1Bor
(B6.129P2-Pctptm1Bor)
|
increased macrophage apoptosis
|
J:115284
|
Pcxtm1c(EUCOMM)Wtsi/Pcxtm1c(EUCOMM)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * C57BL/6N * DBA * SJL)
|
abnormal fatty acid oxidation
|
J:332296
|
abnormal mitochondrial physiology
|
J:332296
|
Pdap1em1Rkuhn/Pdap1em1Rkuhn Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N)
|
abnormal mitochondrial physiology
|
J:298705
|
increased B cell apoptosis
|
J:298705
|
Pdcd1tm1.1Liux/Pdcd1tm1.1Liux
(involves: C57BL/6)
|
decreased cell proliferation
|
J:190150
|
increased apoptosis
|
J:190150
|
Pdcd1tm1.1Liux/Pdcd1tm1.1Liux Tg(MMTV-PyVT)634Mul/0
(involves: C57BL/6 * FVB/N)
|
increased apoptosis
|
J:190150
|
Pdcd1tm1.1Shr/Pdcd1tm1.1Shr Tg(TcraTcrb)1100Mjb/0
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:153040
|
increased T cell proliferation
|
J:153040
|
Pdcd1tm1Hon/Pdcd1tm1Hon
(involves: 129S2/SvPas * C57BL/6)
|
increased B cell proliferation
|
J:50688
|
Pdcd1lg2tm1Dmp/Pdcd1lg2tm1Dmp
(C.129-Pdcd1lg2tm1Dmp)
|
decreased T cell proliferation
|
J:99212
|
Pdcd6iptm1.2Adz/Pdcd6iptm1.2Adz
(either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6))
|
abnormal brain ependyma motile cilium location or orientation
|
J:238436
|
abnormal brain ependyma motile cilium morphology
|
J:238436
|
abnormal brain ependyma motile cilium physiology
|
J:238436
|
Pdcd10tm1Wami/Pdcd10tm1Wami Tg(GFAP-cre)25Mes/0
(involves: 129 * C57BL/6 * FVB/N)
|
abnormal vascular endothelial cell migration
|
J:170480
|
Pdcl2em1Ncvc/Pdcl2em1Ncvc
(involves: C57BL/6 * DBA/2)
|
abnormal acrosome assembly
|
J:338084
|
abnormal sperm axoneme morphology
|
J:338084
|
abnormal sperm flagellum morphology
|
J:338084
|
abnormal sperm head morphology
|
J:338084
|
abnormal sperm midpiece morphology
|
J:338084
|
abnormal sperm nucleus morphology
|
J:338084
|
absent acrosome
|
J:338084
|
detached acrosome
|
J:338084
|
globozoospermia
|
J:338084
|
immotile sperm
|
J:338084
|
Pdcl2em1Ncvc/Pdcl2em1Ncvc Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
(involves: C57BL/6 * DBA/2)
|
abnormal sperm flagellum morphology
|
J:338084
|
Pde3atm1Vman/Pde3atm1Vman
(either: (involves: 129X1/SvJ * C57BL/6J) or (involves: 129X1/SvJ * Black Swiss * C57BL/6J))
|
abnormal female meiosis
|
J:91348
|
Pde4benu1H/Pde4benu1H
(B6.C(C3H)-Pde4benu1H)
|
abnormal neuron differentiation
|
J:223217
|
Pde4btm1Mct/Pde4btm1Mct
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:94853
|
Pde4dtm1Mct/Pde4dtm1Mct
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:94853
|
Pdgfbtm1Cbet/Pdgfbtm1Cbet
(involves: 129P2/OlaHsd * C57BL/6)
|
absent mesangial cell
|
J:20017
|
decreased mesangial cell number
|
J:20017
|
Pdgfbtm1Cbet/Pdgfbtm2Cbet Tg(Tie1-cre)9Ref/0
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
decreased mesangial cell number
|
J:89186
|
Pdgfbtm3.1Cbet/Pdgfbtm3.1Cbet
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased mesangial cell number
|
J:84701
|
Pdgfratm1.1(EGFP/cre/ERT2)Hyma/Pdgfra+
(involves: C57BL/6 * CBA/JNCrlj)
|
cellular phenotype
|
J:221424
|
Pdgfratm1Sor/Pdgfratm1Sor
(either: 129S4/SvJaeSor-Pdgfratm1Sor or (involves: 129S4/SvJaeSor * C57BL/6J))
|
increased apoptosis
|
J:41814
|
Pdgfratm2Sor/Pdgfratm2Sor
(either: 129S4/SvJaeSor-Pdgfratm2Sor or (involves: 129S4/SvJaeSor * C57BL/6J))
|
increased apoptosis
|
J:41814
|
Pdgfratm5Sor/Pdgfratm11(EGFP)Sor
(either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6J))
|
decreased oligodendrocyte progenitor number
|
J:73817
|
Pdgfratm6Sor/Pdgfratm11(EGFP)Sor
(either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6J))
|
decreased oligodendrocyte progenitor number
|
J:73817
|
Pdgfratm8Sor/Pdgfratm8Sor Pdgfrbtm1Mdt/Pdgfrbtm1Mdt H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: C57BL/6 * CBA)
|
abnormal cardiac neural crest cell migration
|
J:122584
|
Pdgfratm8Sor/Pdgfratm8Sor Tg(Nr5a1-cre)2Klp/0
(either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6))
|
abnormal spermatocyte morphology
|
J:142042
|
oligozoospermia
|
J:142042
|
Pdgfratm12.1Sor/Pdgfra+
(involves: 129 * C57BL/6)
|
increased cell proliferation
|
J:146617
|
increased fibroblast chemotaxis
|
J:146617
|
increased fibroblast proliferation
|
J:146617
|
increased mesenchymal cell proliferation involved in lung development
|
J:146617
|
Pdgfratm13.1Sor/Pdgfra+
(involves: 129 * C57BL/6)
|
increased fibroblast proliferation
|
J:146617
|
Pdgfrbredeye/Pdgfrbredeye
(C3N.C-Pdgfrbredeye)
|
abnormal basement membrane morphology
|
J:199483
|
increased retina apoptosis
|
J:199483
|
Pdgfrbtm1Msas/Pdgfrbtm1Msas
(involves: 129 * C57BL/6)
|
decreased cell proliferation
|
J:110798
|
increased apoptosis
|
J:110798
|
Pdgfrbtm1Msas/Pdgfrbtm1Msas Tg(Nes-cre)1Nogu/?
(involves: 129 * C57BL/6)
|
increased susceptibility to neuronal excitotoxicity
|
J:110616
|
Pdgfrbtm1Rheu/Pdgfrbtm1Rheu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal fibroblast migration
|
J:93973
|
decreased fibroblast apoptosis
|
J:93973
|
Pdgfrbtm1Sor/Pdgfrbtm1Sor
(either: 129S7/SvEvBrd-Pdgfrbtm1Sor or (involves: 129S7/SvEvBrd * C57BL/6J))
|
absent mesangial cell
|
J:20016
|
Pdgfrbtm1Sor/Pdgfrbtm5Sor
(either: (involves: 129S4/SvJaeSor * 129S7/SvEvBrd) or (involves: 129S4/SvJaeSor * 129S7/SvEvBrd * C57BL/6))
|
abnormal mesangial cell morphology
|
J:67735
|
Pdgfrbtm2Sor/Pdgfrbtm2Sor
(either: 129S7/SvEvBrd-Pdgfrbtm2Sor or (involves: 129S7/SvEvBrd * C57BL/6J))
|
absent mesangial cell
|
J:20016
|
Pdgfrbtm4Sor/Pdgfrbtm4Sor
(either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6))
|
abnormal mesangial cell morphology
|
J:66516
|
decreased fibroblast proliferation
|
J:66516
|
decreased kidney cell proliferation
|
J:66516
|
Pdgfrbtm14(Pdgfrb)Sor/Pdgfrb+ Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S4/SvJaeSor * C57BL/6 * CBA)
|
abnormal white fat cell differentation
|
J:173602
|
Pdgfrbtm14(Pdgfrb)Sor/Pdgfrb+ Tg(Tagln-cre)1Her/0
(involves: 129S4/SvJaeSor * C57BL/6 * SJL)
|
increased vascular smooth muscle cell proliferation
|
J:173602
|
Pdha1tm1Ptl/Pdha1tm1Ptl Tg(Zp3-cre)93Knw/0
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal female meiosis
|
J:123893
|
abnormal oocyte morphology
|
J:123893
|
abnormal polar body morphology
|
J:123893
|
impaired spindle assembly in female meiosis
|
J:123893
|
Pdia3Gt(RST003)Byg/Pdia3Gt(RST003)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:160036
|
Pdia3Gt(RST003)Byg/Pdia3Gt(RST003)Byg
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:178553
|
Pdia4tm1b(EUCOMM)Wtsi/Pdia4tm1b(EUCOMM)Wtsi Tg(Pf4-icre)Q3Rsko/0
(involves: C57BL/6N)
|
decreased platelet ATP level
|
J:244748
|
Pdilttm1Osb/Pdilttm1Osb
(involves: 129S2/SvPas)
|
impaired sperm migration in female genital tract
|
J:182133
|
Pdk4tm1Tok/Pdk4tm1Tok
(B6.129P2-Pdk4tm1Tok)
|
abnormal osteoclast differentiation
|
J:179789
|
Pdpk1tm1.1Mlw/Pdpk1tm1.1Mlw Rag2tm1Fwa/Rag2tm1Fwa Tnfrsf4tm2(cre)Nik/Tnfrsf4+ Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+
(involves: 129S/SvEv * 129X1/SvJ * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:226194
|
Pdpk1tm1.1Mlw/Pdpk1tm1.1Mlw Tnfrsf4tm2(cre)Nik/Tnfrsf4+ Gt(ROSA)26Sortm1(EYFP)Cos/Gt(ROSA)26Sor+
(involves: 129X1/SvJ * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:226194
|
Pdpk1tm1.2Mlw/Pdpk1tm1.2Mlw
(involves: BALB/c)
|
abnormal neural crest cell physiology
|
J:85894
|
Pdpk1tm1Maka/Pdpk1tm1Maka Tg(CAG-cat,-lacZ)11Miya/0 Tg(Pomc1-cre)16Lowl/0
(involves: 129S4/SvJae * C57BL/6 * DBA/2 * FVB/N)
|
increased corticotroph apoptosis
|
J:162892
|
increased melanotroph apoptosis
|
J:162892
|
increased pituitary gland apoptosis
|
J:162892
|
Pdpk1tm1Maka/Pdpk1tm1Maka Tg(Zp3-cre)93Knw/0
(involves: 129S4/SvJae * C57BL/6J)
|
maternal effect
|
J:165798
|
Pdpk1tm1Mlw/Pdpk1tm1Mlw Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:165626
|
Pds5atm1.1Alos/Pds5atm1.1Alos
(involves: 129S2/SvPas)
|
abnormal mitosis
|
J:205601
|
Pds5btm1.2Alos/Pds5btm1.2Alos
(involves: 129S2/SvPas)
|
abnormal cell nucleus morphology
|
J:205601
|
abnormal chromosome morphology
|
J:205601
|
abnormal mitosis
|
J:205601
|
aneuploidy
|
J:205601
|
decreased cell proliferation
|
J:205601
|
Pds5btm1Jmi/Pds5btm1Jmi
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased germ cell number
|
J:124279
|
decreased male germ cell number
|
J:124279
|
Pdss2kd/Pdss2kd
(CBA/H-Pdss2kd)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:197578
|
abnormal respiratory electron transport chain
|
J:197578
|
decreased hepatocyte mitochondrial DNA content
|
J:197578
|
decreased mitochondrial DNA content
|
J:197578
|
increased mitochondrial DNA content
|
J:197578
|
oxidative stress
|
J:197578
|
Pdss2kd/Pdss2kd
(B6.CBACaH(CAST)-Pdss2kd)
|
abnormal mitochondrial morphology
|
J:101779
|
Pdss2kd/Pdss2kd
(involves: C57BL/6 * CBA/H)
|
abnormal cellular respiration
|
J:136670
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:136670
|
Pdss2tm1.1Jdhu/Pdss2tm1.2Jdhu Tg(Pax2-cre)1Akg/0
(involves: 129 * C57BL/6N * FVB/N)
|
abnormal cell morphology
|
J:179845
|
abnormal mitochondrial morphology
|
J:179845
|
abnormal Purkinje cell migration
|
J:179845
|
abnormal radial glial cell morphology
|
J:179845
|
decreased radial glial cell number
|
J:179845
|
increased neuron apoptosis
|
J:179845
|
Pdss2tm1Dalg/Pdss2tm1Dalg Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal aerobic respiration
|
J:136670
|
abnormal mitophagy
|
J:136670
|
abnormal respiratory electron transport chain
|
J:136670
|
Pdx1tm1Cvw/Pdx1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased pancreatic beta cell apoptosis
|
J:165268
|
Pdx1tm1Cvw/Pdx1tm1Cvw
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss)
|
abnormal pancreatic beta cell differentiation
|
J:32017
|
Pdx1tm1Cvw/Pdx1tm4Cvw Tg(Ins2-cre)25Mgn/0
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss * C57BL/6 * DBA)
|
decreased pancreatic beta cell proliferation
|
J:130389
|
increased pancreatic alpha cell proliferation
|
J:130389
|
Pdx1tm1Egs/Pdx1+ Stk11tm1.1Gne/Stk11tm1.1Gne
(involves: 129S1/Sv * C57BL/6N)
|
increased cell proliferation
|
J:195229
|
Pdx1tm1Macd/Pdx1tm1Macd Tg(tetO-Ipf1,EGFP)956.6Macd/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
increased cell proliferation
|
J:101742
|
Pdx1tm1Ted/Pdx1+
(involves: 129P2/OlaHsd)
|
abnormal pancreatic beta cell apoptosis
|
J:82969
|
abnormal pancreatic islet cell apoptosis
|
J:82969
|
Pdx1tm2Cvw/Pdx1+
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss)
|
abnormal mitochondrial physiology
|
J:75664
|
abnormal tricarboxylic acid cycle
|
J:75664
|
Pdx1tm2Cvw/Pdx1tm2Cvw
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss)
|
abnormal pancreatic beta cell differentiation
|
J:32017
|
Pdzd7tm1a(EUCOMM)Wtsi/Pdzd7tm1a(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal outer hair cell kinocilium location or orientation
|
J:209073
|
Pea15atm1Chne/Pea15atm1Chne
(involves: C57BL/6)
|
increased male germ cell apoptosis
|
J:121558
|
Pecam1tm1Mak/Pecam1tm1Mak
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased lung endothelial cell migration
|
J:110561
|
Peg3tm1.1Jkim/Peg3+
(involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J)
|
abnormal imprinting
|
J:184471
|
cellular phenotype
|
J:184471
|
Peg3tm1a(EUCOMM)Hmgu/Peg3+
(involves: C57BL/6N)
|
decreased oocyte number
|
J:209833
|
Peg3tm1Masu/Peg3+
(involves: 129S1/Sv * 129X1/SvJ)
|
maternal imprinting
|
J:54324
|
Peg10tm1Fuis/Peg10+
(involves: 129S/SvEv)
|
maternal imprinting
|
J:106134
|
Peli1tm1Tigm/Peli1tm1Tigm
(involves: 129/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:152781
|
increased B cell apoptosis
|
J:152781
|
Peli2tm1.1Arte/Peli2tm1.1Arte
(involves: C57BL/6)
|
increased macrophage apoptosis
|
J:265431
|
Peli3tm1.1Arte/Peli3tm1.1Arte
(involves: C57BL/6NTac)
|
abnormal cell physiology
|
J:188556
|
Pelotm1Imad/Pelotm1Imad
(either: 129 or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J))
|
absent inner cell mass proliferation
|
J:81781
|
aneuploidy
|
J:81781
|
polyploidy
|
J:81781
|
Pelotm1Slac/Pelotm1Slac En1tm2(cre)Wrst/En1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
increased neuron apoptosis
|
J:306384
|
increased neuronal precursor proliferation
|
J:306384
|
Pelotm1Slac/Pelotm1Slac Tg(Atoh1-cre)1Bfri/0
(involves: C57BL/6J * CBA)
|
increased neuronal precursor proliferation
|
J:306384
|
Pepddal/Pepddal
(CBA/J-Pepddal/GrsrJ)
|
decreased oocyte number
|
J:87005
|
Per1tm1Brd/Per1tm1Brd Per2tm1Brd/Per2tm1Brd
(involves: 129S7/SvEvBrd)
|
abnormal fibroblast physiology
|
J:193286
|
increased osteoblast proliferation
|
J:115188
|
Per2tm1Brd/Per2tm1Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:79456
|
Per2tm1Ccl/Per2tm1Ccl
(involves: 129 * C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:79456
|
Per2tm1Drw/Per2tm1Drw
(B6.129-Per2tm1Drw/J)
|
decreased hematopoietic stem cell proliferation
|
J:208598
|
Perptm1Att/Perptm1Att
(involves: 129S4/SvJae)
|
decreased cellular sensitivity to gamma-irradiation
|
J:86549
|
decreased neuron apoptosis
|
J:86549
|
decreased thymocyte apoptosis
|
J:86549
|
Perptm2Att/Perptm2Att Tg(KRT14-cre/ERT2)1Ipc/0
(involves: 129S4/SvJae)
|
decreased keratinocyte apoptosis
|
J:167545
|
Pex1tm1.1Hrw/Pex1tm1.1Hrw
(involves: C57BL/6NTac)
|
abnormal mitochondrial crista morphology
|
J:278655
|
abnormal mitochondrial physiology
|
J:278655
|
abnormal peroxisome morphology
|
J:278655
|
dilated mitochondrion
|
J:278655
|
Pex5tm1Pec/Pex5tm1Pec Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA)
|
abnormal cell morphology
|
J:112503
|
abnormal endoplasmic reticulum morphology
|
J:112503
|
abnormal fatty acid beta-oxidation
|
J:121804
|
abnormal lysosome morphology
|
J:112503
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:112503
|
abnormal mitochondrial crista morphology
|
J:112503
|
abnormal mitochondrial inner membrane morphology
|
J:112503
|
abnormal mitochondrial shape
|
J:112503
|
abnormal respiratory electron transport chain
|
J:112503
|
Pex7tm1Nbra/Pex7tm1Nbra
(involves: 129S/SvEv * C57BL/6)
|
abnormal cell physiology
|
J:158845
|
Pex7tm1Rjaw/Pex7tm1Rjaw
(Swiss)
|
abnormal neuronal migration
|
J:92346
|
Pex10m1Nisw/Pex10m1Nisw
(129S1.B6-Pex10m1Nisw)
|
abnormal axon extension
|
J:216140
|
abnormal axon fasciculation
|
J:216140
|
Pex11atm1Itl/Pex11atm1Itl
(C57BL/6-Pex11atm1Itl)
|
abnormal cell morphology
|
J:195940
|
Pex11atm1Sjg/Pex11atm1Sjg
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal hepatocyte mitochondrial morphology
|
J:80124
|
abnormal peroxisome morphology
|
J:80124
|
Pex11atm1Sjg/Pex11atm1Sjg Pex11btm1Sjg/Pex11btm1Sjg
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal peroxisome morphology
|
J:80124
|
abnormal peroxisome physiology
|
J:80124
|
Pex11btm1Sjg/Pex11b+
(B6.129-Pex11btm1Sjg)
|
abnormal neuron differentiation
|
J:180632
|
increased neuron apoptosis
|
J:180632
|
oxidative stress
|
J:180632
|
Pex11btm1Sjg/Pex11btm1Sjg
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal peroxisome morphology
|
J:76782
|
abnormal peroxisome physiology
|
J:76782
|
increased mitochondrial number
|
J:76782
|
Pex11btm1Sjg/Pex11btm1Sjg
(B6.129-Pex11btm1Sjg)
|
abnormal neuron differentiation
|
J:180632
|
increased neuron apoptosis
|
J:180632
|
oxidative stress
|
J:180632
|
Pex13tm1.1Crne/Pex13tm1.1Crne
(involves: 129T2/SvEms * C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:84795
|
abnormal mitochondrial morphology
|
J:84795
|
abnormal mitochondrial physiology
|
J:167578
|
abnormal peroxisome morphology
|
J:84795
|
abnormal peroxisome physiology
|
J:84795
|
oxidative stress
|
J:167578
|
Pex13tm1Crne/Pex13tm1.1Crne Tg(Nes-cre)1Kln/0
(involves: 129T2/SvEms * C57BL/6 * C57BL/6J * SJL)
|
abnormal cerebellar granule cell migration
|
J:167578
|
abnormal Purkinje cell differentiation
|
J:167578
|
Pex16tm1c(EUCOMM)Hmgu/Pex16tm1c(EUCOMM)Hmgu Tg(Adipoq-cre)1Evdr/0
(involves: C57BL/6N * FVB/NJ * SJL)
|
abnormal mitochondrial physiology
|
J:270463
|
decreased fat cell mitochondrial DNA content
|
J:270463
|
Pfdn5nmf5a/Pfdn5nmf5a
(C57BL/6-Pfdn5nmf5a)
|
abnormal brain ependyma motile cilium morphology
|
J:167349
|
abnormal retina apoptosis
|
J:167349
|
decreased brain ependyma motile cilium number
|
J:167349
|
necrospermia
|
J:167349
|
oligozoospermia
|
J:167349
|
Pfkfb3tm1.1Pec/Pfkfb3tm1.1Pec Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCrl * CBA)
|
cellular phenotype
|
J:296552
|
gangrene
|
J:296552
|
Pfn1tm1Fgi/Pfn1+
(involves: 129P2/OlaHsd)
|
abnormal cell morphology
|
J:335495
|
abnormal cell nucleus morphology
|
J:335495
|
abnormal mitotic cytokinesis
|
J:335495
|
binucleate
|
J:335495
|
increased cell nucleus count
|
J:335495
|
Pfn1tm1Foxp/Pfn1tm1Foxp Tg(Tek-cre)1Ywa/0
(involves: C57BL/6 * C57BL/6NTac * SJL)
|
abnormal vascular endothelial cell migration
|
J:193938
|
Pfn2tm1Wit/Pfn2tm1Wit
(Not Specified)
|
abnormal cell physiology
|
J:122603
|
Pfn3em1Hsc/Pfn3+
(involves: C57BL/6 * DBA)
|
abnormal sperm head morphology
|
J:320651
|
abnormal sperm nucleus morphology
|
J:320651
|
oligozoospermia
|
J:320651
|
Pfn3em1Hsc/Pfn3em1Hsc
(involves: C57BL/6 * DBA)
|
abnormal acrosome assembly
|
J:320651
|
abnormal acrosome morphology
|
J:320651
|
abnormal Golgi apparatus morphology
|
J:320651
|
abnormal Golgi vesicle transport
|
J:320651
|
abnormal manchette assembly
|
J:320651
|
abnormal proacrosomal vesicle fusion
|
J:320651
|
abnormal sperm connecting piece morphology
|
J:320651
|
abnormal sperm flagellum morphology
|
J:320651
|
abnormal sperm head morphology
|
J:320651
|
abnormal sperm midpiece morphology
|
J:320651
|
abnormal sperm mitochondrial morphology
|
J:320651
|
abnormal sperm mitochondrial sheath morphology
|
J:320651
|
abnormal sperm nucleus morphology
|
J:320651
|
asthenozoospermia
|
J:320651
|
decreased sperm progressive motility
|
J:320651
|
detached acrosome
|
J:320651
|
globozoospermia
|
J:320651
|
impaired autophagy
|
J:320651
|
necrospermia
|
J:320651
|
oligozoospermia
|
J:320651
|
Pfn3em2Hsc/Pfn3+
(involves: C57BL/6 * DBA)
|
abnormal sperm head morphology
|
J:320651
|
abnormal sperm nucleus morphology
|
J:320651
|
oligozoospermia
|
J:320651
|
Pfn3em2Hsc/Pfn3em2Hsc
(involves: C57BL/6 * DBA)
|
abnormal acrosome assembly
|
J:320651
|
abnormal acrosome morphology
|
J:320651
|
abnormal Golgi apparatus morphology
|
J:320651
|
abnormal Golgi vesicle transport
|
J:320651
|
abnormal manchette assembly
|
J:320651
|
abnormal proacrosomal vesicle fusion
|
J:320651
|
abnormal sperm connecting piece morphology
|
J:320651
|
abnormal sperm flagellum morphology
|
J:320651
|
abnormal sperm head morphology
|
J:320651
|
abnormal sperm midpiece morphology
|
J:320651
|
abnormal sperm mitochondrial morphology
|
J:320651
|
abnormal sperm mitochondrial sheath morphology
|
J:320651
|
abnormal sperm nucleus morphology
|
J:320651
|
asthenozoospermia
|
J:320651
|
decreased sperm progressive motility
|
J:320651
|
detached acrosome
|
J:320651
|
globozoospermia
|
J:320651
|
impaired autophagy
|
J:320651
|
necrospermia
|
J:320651
|
oligozoospermia
|
J:320651
|
Pfn3em3Hsc/Pfn3+
(involves: C57BL/6 * DBA)
|
abnormal sperm head morphology
|
J:320651
|
abnormal sperm nucleus morphology
|
J:320651
|
oligozoospermia
|
J:320651
|
Pfn3em3Hsc/Pfn3em3Hsc
(involves: C57BL/6 * DBA)
|
abnormal acrosome assembly
|
J:320651
|
abnormal acrosome morphology
|
J:320651
|
abnormal Golgi apparatus morphology
|
J:320651
|
abnormal Golgi vesicle transport
|
J:320651
|
abnormal manchette assembly
|
J:320651
|
abnormal proacrosomal vesicle fusion
|
J:320651
|
abnormal sperm connecting piece morphology
|
J:320651
|
abnormal sperm flagellum morphology
|
J:320651
|
abnormal sperm head morphology
|
J:320651
|
abnormal sperm midpiece morphology
|
J:320651
|
abnormal sperm mitochondrial morphology
|
J:320651
|
abnormal sperm mitochondrial sheath morphology
|
J:320651
|
abnormal sperm nucleus morphology
|
J:320651
|
asthenozoospermia
|
J:320651
|
decreased sperm progressive motility
|
J:320651
|
detached acrosome
|
J:320651
|
globozoospermia
|
J:320651
|
impaired autophagy
|
J:320651
|
necrospermia
|
J:320651
|
oligozoospermia
|
J:320651
|
Pfn4em1Hsc/Pfn4em1Hsc
(C57BL/6J-Pfn4em1Hsc)
|
abnormal acrosome assembly
|
J:328252
|
abnormal acrosome morphology
|
J:328252
|
abnormal Golgi apparatus morphology
|
J:328252
|
abnormal Golgi vesicle transport
|
J:328252
|
abnormal manchette assembly
|
J:328252
|
abnormal manchette morphology
|
J:328252
|
abnormal proacrosomal vesicle fusion
|
J:328252
|
abnormal sperm connecting piece morphology
|
J:328252
|
abnormal sperm flagellum morphology
|
J:328252
|
abnormal sperm head morphology
|
J:328252
|
abnormal sperm midpiece morphology
|
J:328252
|
abnormal sperm mitochondrial sheath morphology
|
J:328252
|
abnormal sperm nucleus morphology
|
J:328252
|
abnormal spermatid morphology
|
J:328252
|
absent manchette
|
J:328252
|
asthenozoospermia
|
J:328252
|
cellular phenotype
|
J:328252
|
coiled sperm flagellum
|
J:328252
|
decreased sperm progressive motility
|
J:328252
|
globozoospermia
|
J:328252
|
impaired autophagy
|
J:328252
|
necrospermia
|
J:328252
|
small sperm head
|
J:328252
|
Pfn4em2Hsc/Pfn4em2Hsc
(C57BL/6J-Pfn4em2Hsc)
|
abnormal acrosome assembly
|
J:328252
|
abnormal acrosome morphology
|
J:328252
|
abnormal Golgi apparatus morphology
|
J:328252
|
abnormal Golgi vesicle transport
|
J:328252
|
abnormal manchette assembly
|
J:328252
|
abnormal manchette morphology
|
J:328252
|
abnormal proacrosomal vesicle fusion
|
J:328252
|
abnormal sperm connecting piece morphology
|
J:328252
|
abnormal sperm flagellum morphology
|
J:328252
|
abnormal sperm head morphology
|
J:328252
|
abnormal sperm midpiece morphology
|
J:328252
|
abnormal sperm mitochondrial sheath morphology
|
J:328252
|
abnormal sperm nucleus morphology
|
J:328252
|
abnormal spermatid morphology
|
J:328252
|
absent manchette
|
J:328252
|
asthenozoospermia
|
J:328252
|
cellular phenotype
|
J:328252
|
coiled sperm flagellum
|
J:328252
|
decreased sperm progressive motility
|
J:328252
|
globozoospermia
|
J:328252
|
impaired autophagy
|
J:328252
|
necrospermia
|
J:328252
|
small sperm head
|
J:328252
|
Pgam5tm1a(EUCOMM)Wtsi/Pgam5tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal mitochondrial crista morphology
|
J:225345
|
abnormal mitochondrial morphology
|
J:225345
|
abnormal mitochondrial physiology
|
J:225345
|
oxidative stress
|
J:225345
|
Pgam5tm1d(EUCOMM)Wtsi/Pgam5tm1d(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal mitochondrial morphology
|
J:240016
|
abnormal mitochondrial shape
|
J:240016
|
abnormal redox activity
|
J:240016
|
cellular phenotype
|
J:240016
|
Pgap1m1Nisw/Pgap1m1Nisw Tg(Hhex-EGFP)#Rbe/0
(involves: C57BL/6 * C57BL/6J * CBA/J)
|
abnormal anterior visceral endoderm cell migration
|
J:187360
|
Pgap1tm1Osb/Pgap1tm1Osb
(involves: 129S2/SvPas)
|
impaired sperm migration in female genital tract
|
J:126766
|
Pgap3tm1.1Ymra/Pgap3tm1.1Ymra
(involves: 129 * C57BL/6)
|
decreased T cell proliferation
|
J:181221
|
increased T cell proliferation
|
J:181221
|
Pgap3tm1.1Ymra/Pgap3tm1.1Ymra
(B6.Cg-Pgap3tm1.1Ymra)
|
decreased B cell proliferation
|
J:203443
|
impaired macrophage phagocytosis
|
J:203443
|
Pggt1btm1.1Mbrg/Pggt1btm1.1Mbrg
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal cell migration
|
J:122107
|
abnormal cell morphology
|
J:122107
|
Pggt1btm1Mbrg/Pggt1btm1Mbrg
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
absent fibroblast proliferation
|
J:122107
|
Pggt1btm1Mbrg/Pggt1btm1Mbrg Krastm4Tyj/Kras+
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal cell morphology
|
J:122107
|
decreased cell proliferation
|
J:122107
|
Pggt1btm1Mbrg/Pggt1btm1Mbrg Tg(KRT14-cre)1Amc/?
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased keratinocyte proliferation
|
J:158528
|
Pgk2tm1Dao/Pgk2tm1Dao
(involves: 129S6/SvEvTac * C57BL/6NCrl)
|
asthenozoospermia
|
J:156646
|
decreased sperm progressive motility
|
J:156646
|
Pglyrp1tm1Rdz/Pglyrp1tm1Rdz
(involves: 129S5/SvEvBrd * BALB/c)
|
abnormal intestinal goblet cell morphology
|
J:178053
|
Pglyrp2tm1Rdz/Pglyrp2tm1Rdz
(involves: 129S/SvEv * BALB/c)
|
abnormal intestinal goblet cell morphology
|
J:178053
|
Pglyrp3tm1Rdz/Pglyrp3tm1Rdz
(involves: 129S6/SvEvTac * BALB/c)
|
abnormal intestinal goblet cell morphology
|
J:178053
|
Pglyrp4tm1Rdz/Pglyrp4tm1Rdz
(involves: 129S6/SvEvTac * BALB/c)
|
abnormal intestinal goblet cell morphology
|
J:178053
|
Pgptm1.2Ango/Pgptm1.2Ango
(involves: 129S4/SvJaeSor * C57BL/6J * FVB/N)
|
abnormal cell physiology
|
J:259970
|
abnormal fibroblast proliferation
|
J:259970
|
Pgrtm1Bwo/Pgrtm1Bwo
(involves: 129S7/SvEvBrd)
|
decreased mammary gland epithelial cell proliferation
|
J:85196
|
Pgrtm1Bwo/Pgrtm1Bwo
(involves: 129S7/SvEvBrd * C57BL/6J)
|
increased pancreatic beta cell proliferation
|
J:125584
|
Pgrtm2(cre)Lyd/Pgr+ Wnt5atm1.1Tpy/Wnt5atm1.1Tpy
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal trophoblast giant cell proliferation
|
J:233595
|
Phactr4humdy/Phactr4humdy
(C.B6-Phactr4humdy)
|
abnormal cell cycle
|
J:123924
|
Phb2tm1Tlan/Phb2tm1Tlan
(involves: C57BL/6 * SJL)
|
abnormal mitochondrial morphology
|
J:131699
|
decreased fibroblast proliferation
|
J:131699
|
increased sensitivity to induced cell death
|
J:131699
|
Phc2tm1Hko/Phc2tm1Hko
(B6.129-Phc2tm1Hko)
|
decreased fibroblast proliferation
|
J:100027
|
Phc2tm1Hko/Phc2tm1Hko
(involves: 129S1/Sv * 129X1/SvJ)
|
early cellular replicative senescence
|
J:170279
|
PhexHyp/Phex+
(B6.Cg-PhexHyp/J)
|
cellular phenotype
|
J:87808
|
PhexHyp/PhexHyp
(B6.Cg-PhexHyp/J)
|
maternal effect
|
J:87808
|
PhexPug/Y
(involves: C57BL/6J)
|
decreased chondrocyte apoptosis
|
J:136463
|
Phf6em1Wencc/Y Tg(Vav1-cre)#Cgp/0
(Not Specified)
|
increased hematopoietic stem cell proliferation
|
J:278804
|
Phf6em1Wencc/Phf6em1Wencc Tg(Vav1-cre)#Cgp/0
(Not Specified)
|
increased hematopoietic stem cell proliferation
|
J:278804
|
Phf6tm1.1Avo/Y Tg(Tek-cre)1Ywa/0
(involves: C57BL/6 * SJL)
|
increased hematopoietic stem cell proliferation
|
J:276228
|
Phf7em2Osb/Phf7em2Osb Tg(CAG-EGFP,Acr-EGFP)2Osb/0
(involves: 129S2/SvPas * C57BL/6NSlc)
|
abnormal sperm nucleus morphology
|
J:298823
|
asthenozoospermia
|
J:298823
|
oligozoospermia
|
J:298823
|
teratozoospermia
|
J:298823
|
Phf7tm1c(EUCOMM)Hmgu/Phf7tm1c(EUCOMM)Hmgu Tg(Stra8-icre)1Reb/0
(involves: C57BL/6N * FVB/NJ)
|
abnormal sperm head morphology
|
J:298823
|
abnormal sperm nucleus morphology
|
J:298823
|
asthenozoospermia
|
J:298823
|
enlarged sperm head
|
J:298823
|
globozoospermia
|
J:298823
|
oligozoospermia
|
J:298823
|
Phf8tm1.1Hoch/Y
(involves: 129S4/SvJae * C57BL/6)
|
decreased cell proliferation
|
J:248400
|
Phf13Gt(XB691)Byg/Phf13Gt(XB691)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:185876
|
oligozoospermia
|
J:185876
|
Phf14tm1Take/Phf14tm1Take
(B6.Cg-Phf14tm1Take)
|
increased cell proliferation
|
J:184822
|
increased fibroblast proliferation
|
J:184822
|
Phf19tm1.1Ldc/Phf19tm1.1Ldc
(Not Specified)
|
increased hematopoietic stem cell proliferation
|
J:313068
|
Phgdhtm1.1Shfu/Phgdhtm1.1Shfu
(involves: 129P2/OlaHsd * C57BL/6J * FVB/N)
|
abnormal neuron differentiation
|
J:128777
|
PhipGt(RRJ571)Byg/PhipGt(RRJ571)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell physiology
|
J:164354
|
Phlda2tm1Bty/Phlda2tm1Bty
(involves: 129/Sv * C57BL/6)
|
paternal imprinting
|
J:76871
|
Phlda2tm2Bty/Phlda2tm2Bty
(involves: 129/Sv * C57BL/6)
|
paternal imprinting
|
J:76871
|
Phox2atm1.1Sgu/Phox2atm1.1Sgu
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal neuron differentiation
|
J:175535
|
Phox2btm1.1Heno/Phox2b+
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * DBA/2))
|
abnormal enteric neural crest cell migration
|
J:190742
|
abnormal neuronal precursor proliferation
|
J:190742
|
decreased enteric neural crest cell proliferation
|
J:190742
|
impaired neuron differentiation
|
J:190742
|
Phox2btm2.1Heno/Phox2b+
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * C57BL/6 * DBA/2))
|
abnormal enteric neural crest cell migration
|
J:190742
|
abnormal neuronal precursor proliferation
|
J:190742
|
decreased enteric neural crest cell proliferation
|
J:190742
|
impaired neuron differentiation
|
J:190742
|
Phox2btm3.1Jbr/Phox2btm3.1Jbr Egr2tm2(cre)Pch/Egr2+
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
abnormal neuron differentiation
|
J:155885
|
Phox2btm3.1Jbr/Phox2btm3.1Jbr Isl1tm1(cre)Tmj/Isl1+
(involves: 129S2/SvPas * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal neuron differentiation
|
J:155885
|
Phyhtm1Safe/Phyhtm1Safe
(involves: 129P2/OlaHsd * 129X1/SvJ * Black Swiss * FVB/N)
|
decreased spermatogonia number
|
J:142512
|
Pi4kam1Btlr/Pi4kam1Btlr
(C57BL/6J-Pi4kam1Btlr)
|
decreased macrophage apoptosis
|
J:265261
|
increased cell death
|
J:265261
|
Pianptm1d(KOMP)Wtsi/Pianptm1d(KOMP)Wtsi
(involves: BALB/cJ * C57BL/6N * SJL)
|
increased neuron apoptosis
|
J:279537
|
premature neuronal precursor differentiation
|
J:279537
|
Pias2Gt(pT1Betageo)1Ruiz/Pias2Gt(pT1Betageo)1Ruiz
(involves: 129P2/OlaHsd * C57BL/6)
|
increased apoptosis
|
J:224819
|
oligozoospermia
|
J:224819
|
Pibf1tm1.1(KOMP)Vlcg/Pibf1tm1.1(KOMP)Vlcg
(C57BL/6N-Pibf1tm1.1(KOMP)Vlcg/JMmucd)
|
abnormal primary cilium morphology
|
J:307969
|
absent embryonic cilia
|
J:307969
|
Picalmtm1Towa/Picalmtm1Towa
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal cell physiology
|
J:185312
|
Pick1tm1Rlh/Pick1tm1Rlh
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal acrosome morphology
|
J:149846,
J:233657
|
abnormal sperm mitochondrial sheath morphology
|
J:149846
|
abnormal sperm nucleus morphology
|
J:149846,
J:233657
|
asthenozoospermia
|
J:149846
|
globozoospermia
|
J:149846
|
increased male germ cell apoptosis
|
J:149846
|
oligozoospermia
|
J:149846
|
teratozoospermia
|
J:149846
|
Pierce1tm2b(EUCOMM)Wtsi/Pierce1tm2b(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal motile primary cilium physiology
|
J:316131
|
abnormal respiratory motile cilium physiology
|
J:316131
|
Pierce2em1(IMPC)H/Pierce2em1(IMPC)H
(involves: C57BL/6N)
|
abnormal motile primary cilium physiology
|
J:316131
|
Pif1tm1Leah/Pif1tm1Leah
(involves: 129P2/OlaHsd * C57BL/6)
|
increased telomere length
|
J:118302
|
Pigatm1Tak/Pigatm1Tak Tg(Zp3-cre)1Gwh/0
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal gametes
|
J:83792
|
Pigatm2Tak/Y
(chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal plasma membrane morphology
|
J:32798
|
Pignm1Nisw/Pignm1Nisw Tg(Hhex-EGFP)#Rbe/0
(involves: 129S1/SvImJ * C3H/HeJ * CBA/J * C57BL/6 * C57BL/6J)
|
abnormal anterior visceral endoderm cell migration
|
J:187360
|
Pik3ap1tm1Kuro/Pik3ap1tm1Kuro
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:84669
|
Pik3c2atm1Bvan/Pik3c2a+
(involves: C57BL/6)
|
abnormal plasma membrane morphology
|
J:226344
|
Pik3c3tm1.1Fawa/Pik3c3tm1.1Fawa
(involves: 129S4/SvJaeSor * C57BL/6J)
|
cellular phenotype
|
J:169569
|
decreased cell proliferation
|
J:169569
|
Pik3c3tm1.1Flv/Pik3c3tm1.1Flv Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * C57BL/6N * DBA/2)
|
abnormal autophagy
|
J:184753
|
Pik3c3tm1.1Flv/Pik3c3tm1.1Flv Tg(Cd8a-cre)1Itan/0
(involves: C57BL/6 * C57BL/6N)
|
abnormal mitochondrial morphology
|
J:184753
|
abnormal mitochondrial physiology
|
J:184753
|
increased T cell apoptosis
|
J:184753
|
oxidative stress
|
J:184753
|
Pik3c3tm1c(EUCOMM)Wtsi/Pik3c3tm1c(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal autophagy
|
J:182628
|
abnormal vacuole morphology
|
J:182628
|
decreased cell proliferation
|
J:182628
|
Pik3c3tm1c(EUCOMM)Wtsi/Pik3c3tm1c(EUCOMM)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: C57BL/6 * C57BL/6N * C57BL/6NCrj * DBA)
|
abnormal autophagy
|
J:182628
|
Pik3c3tm1c(EUCOMM)Wtsi/Pik3c3tm1c(EUCOMM)Wtsi Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: C57BL/6N * C57BL/6NCrj)
|
abnormal autophagy
|
J:182628
|
Pik3c3tm1c(EUCOMM)Wtsi/Pik3c3tm1c(EUCOMM)Wtsi Tg(CAG-EGFP/Map1lc3b)53Nmz/0 Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6N * C57BL/6NCrj * FVB/N)
|
abnormal autophagy
|
J:182628
|
Pik3c3tm1Tssk/Pik3c3tm1Tssk Tg(Cryaa-cre)10Mlr/0
(involves: FVB/N)
|
impaired autophagy
|
J:198392
|
Pik3catm1.1Jjz/Pik3catm1.1Jjz
(involves: C57BL/6)
|
abnormal cell physiology
|
J:115274
|
Pik3catm1.1Waph/Pik3ca+
(involves: 129S1/Sv * C57BL/6)
|
decreased fibroblast apoptosis
|
J:184382
|
increased fibroblast proliferation
|
J:184382
|
Pik3catm1.1Waph/Pik3ca+ Tg(MMTV-cre)#Mam/0
(involves: 129S1/Sv * C57BL/6 * FVB)
|
increased mammary gland epithelial cell proliferation
|
J:187299
|
Pik3catm1Jjz/Pik3catm1Jjz Tg(Pbsn-cre)4Prb/0
(involves: 129 * C57BL/6 * DBA/2)
|
abnormal cell physiology
|
J:138565
|
Pik3catm1Nbm/Pik3catm1Nbm
(involves: 129S6/SvEvTac)
|
decreased cell proliferation
|
J:54237
|
Pik3cbtm1.1Ehi/Pik3cbtm1.1Ehi
(involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6J)
|
decreased fibroblast proliferation
|
J:152332
|
Pik3cbtm1.1Ehi/Pik3cbtm1.1Ehi
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6J)
|
abnormal spermatogonia proliferation
|
J:165087
|
azoospermia
|
J:165087
|
decreased male germ cell number
|
J:165087
|
decreased spermatogonia number
|
J:165087
|
increased testis apoptosis
|
J:165087
|
oligozoospermia
|
J:165087
|
Pik3cbtm1Jjz/Pik3cbtm1Jjz
(involves: 129 * C57BL/6)
|
abnormal cell physiology
|
J:138565
|
decreased fibroblast proliferation
|
J:138565
|
Pik3cdtm1Jni/Pik3cdtm1Jni
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:80614
|
Pik3cdtm1Tnr/Pik3cdtm1Tnr
(involves: 129S4/SvJae)
|
decreased B cell proliferation
|
J:113491,
J:79133
|
Pik3cdtm1Tnr/Pik3cdtm1Tnr Pik3cgtm1Pngr/Pik3cgtm1Pngr
(B6.129-Pik3cdtm1Tnr Pik3cgtm1Pngr)
|
impaired neutrophil chemotaxis
|
J:134324
|
Pik3cgtm1Dwu/Pik3cgtm1Dwu
(Not Specified)
|
impaired neutrophil chemotaxis
|
J:60348
|
Pik3cgtm1Ehi/Pik3cgtm1Ehi
(Not Specified)
|
impaired macrophage chemotaxis
|
J:91945
|
Pik3cgtm1Lste/Pik3cgtm1Lste
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:147259
|
Pik3cgtm1Lste/Pik3cgtm1Lste
(involves: 129P2/OlaHsd)
|
impaired neutrophil chemotaxis
|
J:238900
|
Pik3cgtm1Pngr/Pik3cgtm1Pngr
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:60347
|
impaired neutrophil chemotaxis
|
J:60347
|
Pik3cgtm1Pngr/Pik3cgtm1Pngr
(B6.129P2-Pik3cgtm1Pngr)
|
impaired neutrophil chemotaxis
|
J:134324
|
Pik3cgtm1Wym/Pik3cgtm1Wym
(either: 129/Sv-Pik3cgtm1Wym or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
impaired macrophage chemotaxis
|
J:60349
|
impaired neutrophil chemotaxis
|
J:60349
|
Pik3cgtm1Wym/Pik3cgtm1Wym
(involves: 129S1/Sv * 129X1/SvJ)
|
impaired neutrophil chemotaxis
|
J:238900
|
Pik3cgtm2Ehi/Pik3cgtm2Ehi
(Not Specified)
|
impaired macrophage chemotaxis
|
J:124856
|
impaired neutrophil chemotaxis
|
J:124856
|
Pik3r1tm1.1Geno/Pik3r1+
(involves: C57BL/6 * C57BL/6J)
|
decreased adipocyte glucose uptake
|
J:234657
|
Pik3r1tm1Dfr/Pik3r1tm1Dfr
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased B cell proliferation
|
J:52229
|
Pik3r1tm1Dfr/Pik3r1tm1Dfr Plcg2tm1Jni/Plcg2tm1Jni
(involves: 129P2/OlaHsd * 129S6/SvEvTac)
|
increased B cell apoptosis
|
J:104166
|
Pik3r1tm1Tka/Pik3r1tm1Tka
(involves: C57BL/6 * CBA)
|
decreased B cell proliferation
|
J:113491,
J:52228
|
increased adipocyte glucose uptake
|
J:52576
|
increased skeletal muscle cell glucose uptake
|
J:52576
|
Pik3r2em1Gldn/Pik3r2em1Gldn
(C57BL/6-Pik3r2em1Gldn)
|
abnormal cell nucleus morphology
|
J:304006
|
Pik3r4mbe/Pik3r4mbe
(involves: C3H/HeH * C57BL/6)
|
abnormal autophagy
|
J:258027
|
abnormal cell physiology
|
J:258027
|
abnormal neuronal migration
|
J:258027
|
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd
(involves: 129S2/SvPas * C57BL/6N)
|
abnormal autophagy
|
J:198770
|
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd
(involves: 129S2/SvPas * C57BL/6)
|
abnormal neuronal migration
|
J:258027
|
Pik3r4tm1.1Mpnd/Pik3r4tm1.1Mpnd Tg(ACTA1-cre)79Jme/0
(involves: 129S2/SvPas * C57BL/6J * C57BL/6N * SJL)
|
abnormal autophagy
|
J:198770
|
Pik3r5tm1Lste/Pik3r5tm1Lste
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:147259
|
Pik3r5tm1Lste/Pik3r5tm1Lste
(involves: 129P2/OlaHsd)
|
impaired neutrophil chemotaxis
|
J:238900
|
Pikfyvetm1.1Ashi/Pikfyvetm1.1Ashi
(involves: C57BL/6)
|
decreased DNA replication
|
J:171129
|
Pikfyvetm1.1Ashi/Pikfyvetm1.1Ashi Tg(Ckm-cre)28Arte/0
(involves: C57BL/6)
|
decreased muscle cell glucose uptake
|
J:199213
|
increased adipocyte glucose uptake
|
J:199213
|
Pikfyvetm1.2Ashi/Pikfyve+
(involves: C57BL/6)
|
abnormal cell morphology
|
J:171129
|
Pilratm1Osb/Pilratm1Osb
(B6.129-Pilratm1Osb)
|
abnormal leukocyte adhesion
|
J:191085
|
Pim1tm1Pwl/Pim1tm1Pwl Pim2tm1Brn/Pim2tm1Brn Pim3tm1Brn/Pim3tm1Brn
(involves: 129P/Ola * FVB/N)
|
decreased B cell proliferation
|
J:91592
|
decreased T cell proliferation
|
J:91592
|
Pim2tm1Brn/Pim2tm1Brn
(involves: 129P/Ola * FVB/N)
|
decreased T cell proliferation
|
J:91592
|
Pin1tm1Tuc/Pin1tm1Tuc
(involves: 129P2/OlaHsd * C57BL/6)
|
azoospermia
|
J:74508
|
Pin1tm1Tuc/Pin1tm1Tuc
(B6.129P2-Pin1tm1Tuc)
|
decreased primordial germ cell number
|
J:83663
|
decreased primordial germ cell proliferation
|
J:83663
|
Pink1tm1.1Wrst/Pink1tm1.1Wrst
(involves: 129S2/SvPas * BALB/cJ * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:183290
|
Pink1tm1.1Wrst/Pink1tm1.1Wrst Tg(Prnp-SNCA*A53T)AAub/?
(involves: 129S2/SvPas * C57BL/6J * FVB/N)
|
abnormal cell physiology
|
J:242309
|
abnormal nucleolus morphology
|
J:242309
|
Pink1tm1Aub/Pink1tm1Aub
(involves: 129S/SvEv)
|
abnormal cellular respiration
|
J:150206
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:150206
|
abnormal mitochondrial physiology
|
J:150206
|
abnormal respiratory electron transport chain
|
J:150206
|
cellular phenotype
|
J:150206
|
Pink1tm1Hbu/Pink1tm1Hbu
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal mitochondrial physiology
|
J:169471
|
Pink1tm1Hlw/Pink1tm1Hlw
(involves: 129 * C57BL/6J)
|
increased sensitivity to induced cell death
|
J:175006
|
oxidative stress
|
J:175006
|
Pink1tm1Lex/Pink1tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cellular respiration
|
J:148988
|
abnormal lysosome morphology
|
J:148903
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:148988
|
increased neuron apoptosis
|
J:148903
|
Pink1tm1Vbae/Pink1tm1Vbae
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:182977
|
abnormal mitochondrial morphology
|
J:182977
|
abnormal mitochondrial physiology
|
J:182977
|
cellular phenotype
|
J:182977
|
oxidative stress
|
J:182977
|
Pink1tm1Zhzh/Pink1tm1Zhzh Slc6a3tm4.1(tTA)Xz/? Tg(tetO-SNCA*A53T)E2Cai/?
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6)
|
abnormal mitochondrial morphology
|
J:218892
|
Pinx1tm1.1Kplu/Pinx1+
(involves: 129S7/SvEvBrd * C57BL/6 * FVB/N)
|
chromosomal instability
|
J:171997
|
increased telomere length
|
J:171997
|
Pinx1tm1.1Kplu/Pinx1+ Terttm1Leah/Terttm1Leah
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * FVB/N)
|
cellular phenotype
|
J:171997
|
Pip4k2ctm1b(KOMP)Wtsi/Pip4k2ctm1b(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
increased T cell proliferation
|
J:234283
|
Pip4p1tm1(KOMP)Wtsi/Pip4p1tm1(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal cell physiology
|
J:274778
|
Pip5k1atm1.1Tba/Pip5k1atm1.1Tba
(involves: 129P2/OlaHsd)
|
abnormal sperm midpiece morphology
|
J:185835
|
asthenozoospermia
|
J:185835
|
Pip5k1atm1.1Tba/Pip5k1atm1.1Tba Pip5k1btm1Tssk/Pip5k1btm1Tssk
(involves: 129P2/OlaHsd)
|
abnormal sperm midpiece morphology
|
J:185835
|
asthenozoospermia
|
J:185835
|
coiled sperm flagellum
|
J:185835
|
detached sperm flagellum
|
J:185835
|
oligozoospermia
|
J:185835
|
Pip5k1cGt(XD096)Byg/Pip5k1cGt(XD096)Byg
(involves: 129P2/OlaHsd)
|
decreased neuronal migration
|
J:131432
|
Pip5k1ctm1.1Ref/Pip5k1ctm1.1Ref
(involves: 129)
|
cellular phenotype
|
J:200273
|
Pip5k1ctm1.2Ref/Pip5k1ctm1.2Ref
(involves: 129)
|
abnormal cell physiology
|
J:200273
|
Pip5k1ctm1.2Ref/Pip5k1ctm1.2Ref Tg(TcraTcrb)425Cbn/0
(involves: BALB/c * C57BL/6)
|
increased T cell proliferation
|
J:164732
|
Pip5k1ctm2.1Ref/Pip5k1ctm2.1Ref
(B6.129-Pip5k1ctm2.1Ref)
|
abnormal cell physiology
|
J:200273
|
Pip5k1ctm2.2Ref/Pip5k1ctm2.2Ref
(involves: 129 * C57BL/6)
|
cellular phenotype
|
J:200273
|
Piptm1Myal/Piptm1Myal
(involves: 129S/SvEv * C57BL/6)
|
increased apoptosis
|
J:202016
|
increased cell proliferation
|
J:202016
|
Pirbtm1Ttk/Pirbtm1Ttk
(involves: 129X1/SvJ)
|
abnormal dendritic cell differentiation
|
J:76770
|
increased B cell proliferation
|
J:76770
|
PisdGt1(Betageo)Jev/PisdGt1(Betageo)Jev
(involves: 129S2/SvPas * C57BL/6)
|
abnormal mitochondrial morphology
|
J:104104
|
Pithd1em1Osb/Pithd1em1Osb
(involves: C57BL/6 * DBA/2)
|
asthenozoospermia
|
J:285040
|
multi-headed sperm
|
J:285040
|
teratozoospermia
|
J:285040
|
Pithd1tm1Ohi/Pithd1tm1Ohi
(involves: C57BL/6N)
|
asthenozoospermia
|
J:285040
|
multi-headed sperm
|
J:285040
|
teratozoospermia
|
J:285040
|
PitpnaGt(OST1152)Lex/PitpnaGt(OST1152)Lex
(involves: 129S5/SvEvBrd)
|
abnormal apoptosis
|
J:85204
|
Pitpnatm1Vab/Pitpnatm1Vab
(involves: 129S7/SvEvBrd)
|
increased hindbrain apoptosis
|
J:85204
|
Pitrm1tm1a(KOMP)Wtsi/Pitrm1+
(C57BL/6N-Pitrm1tm1a(KOMP)Wtsi/Wtsi)
|
abnormal cell physiology
|
J:236767
|
abnormal mitochondrial physiology
|
J:236767
|
Pitx2tm1.1Dmm/Pitx2tm2Sac
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuronal migration
|
J:181058
|
Pitx2tm1Jfm/Pitx2tm4(cre)Jfm
(involves: 129S4/SvJaeSor)
|
abnormal cell migration
|
J:87220
|
Pitx2tm2Sac/Pitx2tm2Sac
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal neuron differentiation
|
J:88779
|
Pitx3tm1.1Cai/Pitx3+ Tg(tetO-SNCA*A53T)E2Cai/0
(involves: 129 * C57BL/6J * FVB/N)
|
abnormal autophagy
|
J:185958
|
Pitx3tm1Mli/Pitx3tm1Mli
(involves: 129P2/OlaHsd)
|
increased neuron apoptosis
|
J:99395
|
Piwil1tm1.1Embrp/Piwil1+
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal spermatid morphology
|
J:182800
|
azoospermia
|
J:182800
|
Piwil1tm1.1Embrp/Piwil1tm1.2Embrp
(involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6)
|
abnormal chromatoid body morphology
|
J:182800
|
Piwil1tm1.2Embrp/Piwil1tm1.2Embrp
(involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6)
|
abnormal chromatoid body morphology
|
J:182800
|
Piwil1tm1Hfl/Piwil1tm1Hfl
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal male germ cell morphology
|
J:77015
|
arrest of male meiosis
|
J:77015
|
Piwil2tm1.1Doca/Piwil2tm1.1Doca
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
abnormal cell physiology
|
J:184034
|
abnormal DNA methylation
|
J:184034
|
abnormal male germ cell apoptosis
|
J:184034
|
arrest of male meiosis
|
J:184034
|
Piwil2tm1.1Doca/Piwil2tm2.1Doca Tg(Stra8-icre)1Reb/0
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ)
|
abnormal cell physiology
|
J:199259
|
abnormal male germ cell apoptosis
|
J:199259
|
Piwil2tm1Nkn/Piwil2tm1Nkn
(involves: 129S2/SvPas * C57BL/6)
|
arrest of male meiosis
|
J:87735
|
azoospermia
|
J:87735
|
increased male germ cell apoptosis
|
J:87735
|
Piwil2tm2.1Doca/Piwil2tm2.1Doca Tg(Stra8-icre)1Reb/0
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J * FVB/NJ)
|
abnormal cell physiology
|
J:199259
|
abnormal male germ cell apoptosis
|
J:199259
|
Piwil2tm2.2Doca/Piwil2tm2.2Doca
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * BALB/cJ * C57BL/6J)
|
abnormal cell physiology
|
J:199259
|
abnormal spermatocyte morphology
|
J:199259
|
abnormal spermatogonia morphology
|
J:199259
|
Piwil4tm1.1Doca/Piwil4tm1.1Doca
(involves: 129P2/OlaHsd * 129S4/SvJaeSor)
|
cellular phenotype
|
J:184034
|
Piwil4tm1Ghan/Piwil4tm1Ghan
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal spermatocyte morphology
|
J:120824
|
arrest of male meiosis
|
J:120824
|
decreased male germ cell number
|
J:120824
|
Pja2tm1.2Afel/Pja2tm1.2Afel
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased mesangial cell number
|
J:345592
|
increased necroptotic process
|
J:345592
|
Pkd1tm1.1Djmp/Pkd1tm1.2Djmp Tg(Cdh16-cre/ERT2)F427Djmp/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6NCrl * FVB/N)
|
increased kidney cell proliferation
|
J:130079
|
Pkd1tm1.1Pcha/Pkd1tm1.1Pcha Pparatm1Gonz/Pparatm1Gonz
(involves: 129 * 129S4/SvJae * C57BL/6)
|
increased kidney cell proliferation
|
J:244067
|
Pkd1tm1.1Pcha/Pkd1tm2Som Tg(Cdh16-cre)91Igr/0
(involves: 129 * 129S4/SvJae * C57BL/6 * ICR)
|
abnormal peroxisome morphology
|
J:244067
|
decreased fatty acid oxidation
|
J:244067
|
increased kidney cell proliferation
|
J:244067
|
oxidative stress
|
J:244067
|
Pkd1tm1.2Djmp/Pkd1+
(involves: 129P2/OlaHsd * FVB/N)
|
increased kidney cell proliferation
|
J:130079
|
Pkd1tm1Jzh/Pkd1tm1Jzh
(either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c))
|
abnormal kidney epithelial cell primary cilium physiology
|
J:81443
|
Pkd1tm1Shh/Pkd1tm1.1Pcha
(involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6)
|
increased cell proliferation
|
J:193544
|
increased kidney epithelial cell primary cilium length
|
J:193544
|
Pkd1tm1Som/Pkd1+ Prkcshtm1Som/Prkcshtm1Som Tg(Cdh16-cre)91Igr/0
(involves: 129 * C57BL/6 * C57BL/6J * ICR * SJL)
|
increased kidney apoptosis
|
J:188763
|
increased kidney cell proliferation
|
J:188763
|
Pkd1tm1Som/Pkd1+ Sec63tm1Som/Sec63tm1Som Tg(Cdh16-cre)91Igr/0
(involves: 129 * C57BL/6 * C57BL/6J * ICR * SJL)
|
increased kidney apoptosis
|
J:188763
|
increased kidney cell proliferation
|
J:188763
|
Pkd1tm1Som/Pkd1tm2Som Tg(Cdh16-cre/ERT2)24Igr/?
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal mitotic spindle morphology
|
J:185863
|
Pkd1tm2Ggg/Pkd1+ Tg(Col1a1-cre)1Bek/0
(involves: 129S4/SvJae * CD-1)
|
impaired osteoblast differentiation
|
J:191967
|
increased osteoblast proliferation
|
J:191967
|
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Col1a1-cre)1Bek/0
(involves: 129S4/SvJae * CD-1)
|
abnormal osteoblast differentiation
|
J:191967
|
increased osteoblast proliferation
|
J:191967
|
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Hoxb7-cre)13Amc/0
(involves: 129S4/SvJae * C57BL/6)
|
increased kidney apoptosis
|
J:171619
|
increased kidney cell proliferation
|
J:171619
|
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Nes-cre)Wme/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
increased kidney apoptosis
|
J:185855
|
increased kidney cell proliferation
|
J:185855
|
Pkd1tm2Som/Pkd1tm2Som Tg(Cdh16-cre)91Igr/0
(involves: 129S4/SvJae * C57BL/6 * ICR)
|
increased kidney cell proliferation
|
J:244067
|
Pkd1tm3Jzh/Pkd1tm3Jzh
(involves: 129P2/OlaHsd * 129X1/SvJ)
|
decreased chondrocyte proliferation
|
J:139970
|
Pkd1tm3Jzh/Pkd1tm3Jzh H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased chondrocyte proliferation
|
J:139970
|
Pkd1tm3Jzh/Pkd1tm3Jzh Tg(Ggt1-cre)M3Egn/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
increased renal tubule apoptosis
|
J:140012
|
Pkd2tm1.1Gwu/Pkd2tm1.1Gwu Tg(Vil1-cre)997Gum/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
increased kidney cell proliferation
|
J:265516
|
Pkd2tm1Som/Pkd2tm2Som
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal cholangiocyte primary cilium morphology
|
J:158354
|
increased cholangiocyte apoptosis
|
J:158354
|
increased kidney apoptosis
|
J:158354
|
increased kidney cell proliferation
|
J:158354
|
Pkd2tm3Som/Pkd2tm3Som Tg(Pkhd1-cre)1Igr/?
(Not Specified)
|
abnormal mitotic spindle morphology
|
J:185863
|
Pkd2tm3Som/Pkd2tm3Som Tg(Pkhd1-cre)1Igr/0
(involves: 129S4/SvJae * C57BL/6)
|
increased kidney cell proliferation
|
J:244067
|
Pkhd1tm1Cjwa/Pkhd1tm1Cjwa
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal cholangiocyte primary cilium morphology
|
J:140302
|
Pkhd1tm1Gwu/Pkhd1tm1Gwu
(Not Specified)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:143394
|
increased mesangial cell number
|
J:143394
|
Pkhd1tm1Gwu/Pkhd1tm1Gwu
(involves: C57BL/6)
|
decreased kidney cell proliferation
|
J:167782
|
increased renal tubule apoptosis
|
J:167782
|
Pkhd1tm1Som/Pkhd1tm1Som
(involves: 129S/SvEv)
|
abnormal mitotic spindle morphology
|
J:185863
|
cellular phenotype
|
J:185863
|
Pkn1tm1Kik/Pkn1tm1Kik
(B6.129P2-Pkn1tm1Kik)
|
decreased activation-induced B cell apoptosis
|
J:193187
|
increased B cell proliferation
|
J:193187
|
increased mesangial cell number
|
J:193187
|
Pkn2tm1a(KOMP)Wtsi/Pkn2tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal fibroblast proliferation
|
J:229595
|
abnormal neural crest cell migration
|
J:229595
|
Pknox1Gt(OST71835)Lex/Pknox1Gt(OST71835)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
increased T cell apoptosis
|
J:103769
|
Pknox1tm1Ngc/Pknox1+ Tg(IghMyc)22Bri/0
(involves: C57BL * SJL)
|
decreased B cell apoptosis
|
J:192251
|
increased B cell proliferation
|
J:192251
|
Pkp1tm2d(KOMP)Wtsi/Pkp1tm2d(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N * SJL/J)
|
abnormal cell adhesion
|
J:233599
|
decreased keratinocyte proliferation
|
J:233599
|
Pkp2tm1Wbm/Pkp2tm1Wbm
(involves: C57BL/6)
|
abnormal cell cytoskeleton morphology
|
J:93314
|
Pkp3tm1.1Fvr/Pkp3tm1.1Fvr
(involves: 129P2/OlaHsd * C57BL/6 * CBA * SJL)
|
increased hair follicle apoptosis
|
J:136451
|
increased keratinocyte apoptosis
|
J:136451
|
increased keratinocyte proliferation
|
J:136451
|
Pla2g2dtm1.1Mhg/Pla2g2dtm1.1Mhg
(B6NCrSlc.Cg-Pla2g2dtm1.1Mhg)
|
abnormal dendritic cell migration
|
J:229035
|
Pla2g3tm1Murm/Pla2g3+
(involves: 129S/SvEv * C57BL/6J)
|
decreased activated sperm motility
|
J:161462
|
decreased sperm progressive motility
|
J:161462
|
Pla2g3tm1Murm/Pla2g3tm1Murm
(involves: 129S/SvEv * C57BL/6J)
|
abnormal acrosome morphology
|
J:161462
|
abnormal outer dense fiber morphology
|
J:161462
|
abnormal sperm axoneme morphology
|
J:161462
|
absent sperm axonemal central pair
|
J:161462
|
biflagellated sperm
|
J:161462
|
coiled sperm flagellum
|
J:161462
|
decreased activated sperm motility
|
J:161462
|
decreased sperm progressive motility
|
J:161462
|
disorganized sperm mitochondrial sheath
|
J:161462
|
globozoospermia
|
J:161462
|
increased sperm mitochondrial size
|
J:161462
|
kinked sperm flagellum
|
J:161462
|
Pla2g3tm1Murm/Pla2g3tm1Murm
(involves: 129S/SvEv * C57BL/6)
|
abnormal mast cell differentiation
|
J:197334
|
decreased mast cell degranulation
|
J:197334
|
Pla2g4atm1Jvb/Pla2g4atm1Jvb
(involves: 129S4/SvJae)
|
abnormal mast cell differentiation
|
J:54619
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:120035
|
increased mast cell degranulation
|
J:54619
|
maternal effect
|
J:39681
|
Pla2g4ftm1.1Itl/Pla2g4ftm1.1Itl
(C.Cg-Pla2g4ftm1.1Itl)
|
cellular phenotype
|
J:278285
|
Pla2g5tm1.1Kiku/Pla2g5tm1.1Kiku
(involves: 129 * C57BL/6)
|
abnormal cardiomyocyte apoptosis
|
J:186024
|
Pla2g5tm1Jarm/Pla2g5tm1Jarm
(involves: 129 * BALB/c)
|
impaired macrophage phagocytosis
|
J:110309
|
Pla2g5tm1Jarm/Pla2g5tm1Jarm
(C.129-Pla2g5tm1Jarm)
|
impaired macrophage phagocytosis
|
J:110309
|
Pla2g5tm1Jarm/Pla2g5tm1Jarm
(involves: 129 * C57BL/6)
|
impaired macrophage phagocytosis
|
J:110309
|
Pla2g5tm1Jarm/Pla2g5tm1Jarm
(B6.129-Pla2g5tm1Jarm)
|
impaired macrophage phagocytosis
|
J:110309
|
Pla2g6tm1.1Hlw/Pla2g6tm1.1Hlw
(involves: 129 * C57BL/6J)
|
abnormal mitochondrial crista morphology
|
J:317126
|
abnormal mitochondrial morphology
|
J:317126
|
abnormal mitochondrial physiology
|
J:317126
|
abnormal mitophagy
|
J:317126
|
decreased mitochondrial size
|
J:317126
|
increased endoplasmic reticulum stress
|
J:317126
|
oxidative stress
|
J:317126
|
Pla2g6tm1Tsu/Pla2g6tm1Tsu
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell cytoskeleton morphology
|
J:174587
|
abnormal mitochondrial crista morphology
|
J:174587
|
abnormal mitochondrial morphology
|
J:174587
|
Pla2g6tm1Turk/Pla2g6tm1Turk
(involves: 129X1/SvJ)
|
asthenozoospermia
|
J:92835
|
Pla2g10tm1Kiku/Pla2g10tm1Kiku
(B6.129P2-Pla2g10tm1Kiku)
|
impaired neutrophil chemotaxis
|
J:155082
|
Pla2g15tm1.1Jash/Pla2g15tm1.1Jash
(involves: 129S1/Sv * C57BL/6)
|
increased macrophage derived foam cell number
|
J:111561
|
Plaaem1Pmi/Plaaem1Pmi
(C57BL/6J-Plaaem1Pmi)
|
abnormal Purkinje cell migration
|
J:240526
|
Plaatm1(NCOM)Cmhd/Plaatm1(NCOM)Cmhd
(either: (involves: C57BL/6J * C57BL/6NTac) or (involves: C57BL/6NTac * CD1))
|
abnormal vesicle-mediated transport
|
J:240526
|
Plaat3tm1.1Hsul/Plaat3tm1.1Hsul
(B6.129P2-Pla2g16tm1.1Hsul)
|
decreased cellular glucose uptake
|
J:239202
|
increased fatty acid oxidation
|
J:239202
|
Plac1tm1(KOMP)Vlcg/Plac1+
(C57BL/6N-Plac1tm1(KOMP)Vlcg)
|
paternal imprinting
|
J:186550
|
Plagl1Gt(OST181461)Lex/Plagl1+
(involves: 129S5/SvEvBrd)
|
paternal imprinting
|
J:171037
|
Plagl1tm1Jour/Plagl1+
(B6.129P2-Plagl1tm1Jour)
|
maternal imprinting
|
J:116147
|
Plagl1tm1Jour/Plagl1+
(CBA.129P2-Plagl1tm1Jour)
|
maternal imprinting
|
J:116147
|
Plast1aCASA/Rk/Plast1aCASA/Rk
(involves: C57BL/6J * CASA/Rk)
|
increased cholesterol efflux
|
J:116492
|
Plast1bCASA/Rk/Plast1bCASA/Rk
(involves: C57BL/6J * CASA/Rk)
|
increased cholesterol efflux
|
J:116492
|
Plattm1Mlg/Plattm1Mlg
(involves: 129S2/SvPas * C57BL/6)
|
cardiac interstitial fibrosis
|
J:95236
|
decreased retina apoptosis
|
J:93533
|
Plattm1Mlg/Plattm1Mlg Plautm1Mlg/Plautm1Mlg
(involves: 129S2/SvPas * C57BL/6)
|
cellular necrosis
|
J:17427
|
Plautm1Mlg/Plautm1Mlg
(involves: 129S2/SvPas * C57BL/6)
|
cardiac interstitial fibrosis
|
J:95236
|
impaired macrophage chemotaxis
|
J:63134
|
impaired neutrophil phagocytosis
|
J:91980
|
Plautm1Mlg/Plautm1Mlg
(B6.Cg-Plautm1Mlg)
|
decreased T cell proliferation
|
J:75303
|
impaired macrophage chemotaxis
|
J:68083
|
Plaurtm1Mlg/Plaurtm1Mlg
(involves: 129S2/SvPas * C57BL/6)
|
impaired neutrophil phagocytosis
|
J:91980
|
Plaurtm1Mlg/Plaurtm1Mlg
(B6.Cg-Plaurtm1Mlg)
|
impaired neuronal migration
|
J:69135
|
Plcb2tm1Dwu/Plcb2tm1Dwu Plcb3tm1Dwu/Plcb3tm1Dwu
(involves: 129S1/Sv * CD-1)
|
increased platelet ATP level
|
J:60348
|
Plcd1tm1Tta/Plcd1tm1Tta
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal keratinocyte differentiation
|
J:83948
|
Plcd1tm1Tta/Plcd1tm1Tta
(involves: 129P2/OlaHsd)
|
abnormal granulocyte differentiation
|
J:205633
|
Plcg1tm1Gcrp/Plcg1tm1Rwen Tg(Cd4-cre)1Cwi/0
(either: B6.Cg-Plcg1tm1Gcrp/Plcg1tm1Rwen Tg(Cd4-cre)1Cwi or (involves: 129X1/SvJ * C57BL/6 * DBA/2))
|
increased T cell proliferation
|
J:157757
|
Plcg2em1Msasn/Plcg2em1Msasn
(B6.Cg-Plcg2em1Msasn/J)
|
abnormal endocytosis
|
J:308279
|
impaired macrophage phagocytosis
|
J:308279
|
Plcg2tm1Jni/Plcg2tm1Jni
(involves: 129P2/OlaHsd)
|
abnormal dendritic cell chemotaxis
|
J:157619
|
decreased B cell proliferation
|
J:80614
|
increased B cell apoptosis
|
J:86373
|
Plcg2tm1Jni/Plcg2tm1Jni
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:114607
|
increased B cell proliferation
|
J:117023
|
Plcg2tm1Kuro/Plcg2tm1Kuro Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
decreased B cell proliferation
|
J:63744
|
Plcl2tm1Tta/Plcl2tm1Tta
(involves: 129P2/OlaHsd)
|
increased B cell proliferation
|
J:85960
|
Pld1tm1.1Gdp/Pld1tm1.1Gdp
(involves: 129/SvJ * C57BL/6)
|
abnormal autophagy
|
J:207283
|
Pld6tm1.1Hsas/Pld6tm1.1Hsas
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal DNA methylation during gametogenesis
|
J:169934
|
abnormal male germ cell apoptosis
|
J:169934
|
abnormal male germ cell morphology
|
J:169934
|
abnormal spermatocyte morphology
|
J:169934
|
arrest of male meiosis
|
J:169934
|
azoospermia
|
J:169934
|
decreased spermatid number
|
J:169934
|
Pld6tm1.1Mafr/Pld6tm1.1Mafr
(involves: C57BL/6)
|
abnormal mitochondrial morphology
|
J:169933
|
abnormal spermatocyte morphology
|
J:169933
|
arrest of male meiosis
|
J:169933
|
Plditm1.2Ploen/Plditm1.2Ploen
(involves: BALB/cJ * C57BL/6)
|
asthenozoospermia
|
J:154651
|
Plectm1Gwi/Plectm4Gwi Tg(Ckmm-cre)5Khn/?
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB)
|
abnormal muscle fiber mitochondrial morphology
|
J:137067
|
Plectm3Gwi/Plectm3Gwi
(involves: 129P2/OlaHsd)
|
abnormal cell morphology
|
J:104701
|
decreased fibroblast cell migration
|
J:104701
|
decreased fibroblast chemotaxis
|
J:104701
|
impaired macrophage chemotaxis
|
J:104701
|
Plectm4Gwi/Plectm4Gwi Tg(Ckmm-cre)5Khn/?
(involves: 129P2/OlaHsd * C57BL/6J * FVB)
|
abnormal muscle fiber mitochondrial morphology
|
J:137067
|
Plectm5Gwi/Plectm5Gwi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal aerobic respiration
|
J:137067
|
Plek2tm1Pji/Plek2tm1Pji
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell differentiation
|
J:257910
|
abnormal granulocyte differentiation
|
J:257910
|
abnormal megakaryocyte differentiation
|
J:257910
|
increased cellular sensitivity to oxidative stress
|
J:257910
|
Plek2tm1Pji/Plek2tm1Pji Jak2tm1.1Ble/Jak2+ Commd10Tg(Vav1-icre)A2Kio/Commd10+
(involves: 129 * C57BL/6 * C57BL/10 * CBA/Ca)
|
abnormal cell differentiation
|
J:257910
|
abnormal granulocyte differentiation
|
J:257910
|
abnormal megakaryocyte differentiation
|
J:257910
|
Plekha1Gt(ROSA)82Sor/Plekha1Gt(ROSA)82Sor
(either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6))
|
abnormal spermatocyte morphology
|
J:142042
|
Plekha1tm1.1Arte/Plekha1tm1.1Arte Plekha2tm1.1Arte/Plekha2tm1.1Arte
(C57BL/6J-Plekha1tm1.1Arte Plekha2tm1.1Arte)
|
increased cardiac muscle cell glucose uptake
|
J:169475
|
increased skeletal muscle cell glucose uptake
|
J:169475
|
Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal male germ cell apoptosis
|
J:189585
|
Plekha5Tg(AMH-cre)1Flor/Plekha5Tg(AMH-cre)1Flor
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal male germ cell apoptosis
|
J:189585
|
abnormal peroxisome physiology
|
J:189585
|
oxidative stress
|
J:189585
|
Plekhf1tm1.1Caox/Plekhf1tm1.1Caox Lyz2tm1(cre)Ifo/Lyz2+
(B6.Cg-Plekhf1tm1.1Caox Lyz2tm1(cre)Ifo)
|
abnormal endocytosis
|
J:277440
|
Plekhm1tm1.2Hzhao/Plekhm1tm1.2Hzhao
(involves: 129S1/Sv * C57BL/6J)
|
abnormal lysosome morphology
|
J:236517
|
decreased lysosomal enzyme secretion
|
J:236517
|
Plekhn1tm1.1Hkon/Plekhn1tm1.1Hkon
(B6.Cg-Plekhn1tm1.1Hkon)
|
abnormal fibroblast physiology
|
J:251603
|
Plekho1tm1Fhe/Plekho1tm1Fhe
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal osteoblast physiology
|
J:145650
|
Plekho2em1Lzhn/Plekho2em1Lzhn
(C57BL/6-Plekho2em1Lzhn)
|
increased macrophage apoptosis
|
J:270531
|
Plet1tm1Cupe/Plet1tm1Cupe
(Not Specified)
|
abnormal dendritic cell migration
|
J:271548
|
Plgtm1Jld/Plgtm1Jld
(involves: 129P2/OlaHsd * NIH Black Swiss)
|
decreased keratinocyte migration
|
J:39419
|
Plgtm1Jld/Plgtm1Jld
(B6.129P2-Plgtm1Jld)
|
increased hepatocyte proliferation
|
J:120368
|
Plgtm1Jld/Plgtm1Jld
(B6.129P2-Plgtm1Jld/J)
|
decreased susceptibility to neuronal excitotoxicity
|
J:141739
|
Plgrkttm1Lmls/Plgrkttm1Lmls
(B6.Cg-Plgrkttm1Lmls)
|
impaired leukocyte migration
|
J:282437
|
impaired macrophage chemotaxis
|
J:282437
|
maternal effect
|
J:282437
|
Plin3tm1.1Jbki/Plin3tm1.1Jbki
(B6J.129S(Cg)-Plin3tm1.1Jbki)
|
abnormal mitochondrial physiology
|
J:261132
|
increased fatty acid oxidation
|
J:261132
|
Plin5tm1e(KOMP)Wtsi/Plin5tm1e(KOMP)Wtsi
(involves: C57BL/6N)
|
decreased adipocyte glucose uptake
|
J:221539
|
decreased fatty acid oxidation
|
J:221539
|
increased fatty acid oxidation
|
J:221539
|
Plin5tm1Macl/Plin5tm1Macl
(involves: 129S6/SvEvTac * C57BL/6JBomTac)
|
decreased fatty acid oxidation
|
J:286482
|
increased cardiac muscle cell glucose uptake
|
J:286482
|
Plin5tm1Tosu/Plin5tm1Tosu
(involves: C57BL/6JJcl)
|
increased fatty acid oxidation
|
J:188390
|
oxidative stress
|
J:188390
|
Plk1Gt(RRR358)Byg/Plk1+
(involves: 129P2/OlaHsd * C57BL/6)
|
aneuploidy
|
J:142593
|
Plk1Gt(RRR358)Byg/Plk1Gt(RRR358)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle
|
J:142593
|
abnormal mitotic spindle morphology
|
J:142593
|
Plk2tm1Rle/Plk2tm1Rle
(either: (involves: 129/Sv * 129S6/SvEvTac) or (involves: 129S6/SvEvTac * MF1))
|
abnormal cell cycle
|
J:85756
|
Plk3tm1Pjs/Plk3tm1Pjs
(involves: 129S6/SvEvTac * Black Swiss)
|
abnormal cell cycle
|
J:175096
|
abnormal cell cycle checkpoint function
|
J:175096
|
polyploidy
|
J:175096
|
Plk4m1Lja/Plk4+
(C57BL/6J-Plk4m1Lja)
|
decreased male germ cell number
|
J:177071
|
Plk4tm1Jwd/Plk4tm1Jwd
(either: 129 or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
abnormal apoptosis
|
J:68142
|
abnormal mitosis
|
J:68142
|
Plod2em1Kaat/Plod2em1Kaat
(involves: C57BL/6 * DBA/2)
|
increased apoptosis
|
J:291131
|
increased endoplasmic reticulum stress
|
J:291131
|
Plod3tm1Rmyl/Plod3tm1Rmyl
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
impaired basement membrane formation
|
J:106510
|
Plod3tm1Soin/Plod3tm1Soin
(involves: 129)
|
abnormal intracellular organelle morphology
|
J:93434
|
Plod3tm2.1Rmyl/Plod3tm2.1Rmyl
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
impaired basement membrane formation
|
J:106510
|
Plod3tm2Rmyl/Plod3tm2Rmyl
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
impaired basement membrane formation
|
J:106510
|
Plp1jp-6J/Y
(BALB/cJ-Plp1jp-6J/GrsrJ)
|
asthenozoospermia
|
J:236909
|
oligozoospermia
|
J:236909
|
Plp1jp-msd/Y
(involves: BALB/c * C3H * C57BL/6 * C57BL/10)
|
increased apoptosis
|
J:121540
|
Plp1jp-rsh/Y
(involves: C3H * C57BL/6 * STOCK Rb(1.3)1Bnr)
|
increased apoptosis
|
J:121540
|
Plp2tm1Dva/Y
(involves: 129 * C57BL/6J)
|
abnormal endoplasmic reticulum morphology
|
J:227053
|
abnormal Golgi vesicle transport
|
J:227053
|
increased endoplasmic reticulum stress
|
J:227053
|
increased fibroblast apoptosis
|
J:227053
|
increased neuron apoptosis
|
J:227053
|
Plpp7em1Eno/Plpp7em1Eno
(involves: C3H * C57BL/6 * C57BL/6N)
|
abnormal cell nucleus morphology
|
J:302139
|
abnormal chromosome morphology
|
J:302139
|
cellular phenotype
|
J:302139
|
Plrg1tm2Jcbr/Plrg1tm2Jcbr
(Not Specified)
|
abnormal cell cycle
|
J:149153
|
decreased cell proliferation
|
J:149153
|
Plrg1tm2Jcbr/Plrg1tm2Jcbr Tg(Ckmm-cre)5Khn/0
(involves: FVB)
|
increased cardiomyocyte apoptosis
|
J:149153
|
Plrg1tm2Jcbr/Plrg1tm2Jcbr Tg(Syn1-cre)671Jxm/0
(involves: C57BL/6 * CBA)
|
increased neuron apoptosis
|
J:149153
|
Pls1tm1Fri/Pls1tm1Fri
(B6.129-Pls1tm1Fri)
|
increased enterocyte apoptosis
|
J:216723
|
Plscr1tm1Lex/Plscr1tm1Lex
(129S/SvEvBrd-Plscr1tm1Lex)
|
abnormal granulocyte differentiation
|
J:76790
|
abnormal neutrophil differentiation
|
J:76790
|
plt/plt
(involves: DDD/1)
|
abnormal leukocyte migration
|
J:47819,
J:47460
|
plt/plt
(B6.DDD-plt)
|
abnormal leukocyte migration
|
J:93960
|
plt/plt
(either: B6.DDD-plt or C.DDD-plt)
|
abnormal leukocyte migration
|
J:110910
|
Pltptm1Jia/Pltptm1Jia
(involves: C57BL/6)
|
asthenozoospermia
|
J:107906
|
Pltptm2.1Jia/Pltptm2.1Jia
(involves: C57BL/6J)
|
abnormal cellular cholesterol metabolism
|
J:239143
|
Plxna1tm1Kik/Plxna1tm1Kik Tg(TcraTcrb)425Cbn/?
(involves: BALB/c * C57BL/6)
|
decreased T cell proliferation
|
J:161856
|
Plxna2nmf454/Plxna2nmf454
(involves: C57BL/6J)
|
decreased neuronal migration
|
J:135408
|
Plxna2tm1Hfu/Plxna2tm1Hfu
(involves: C57BL/6 * CBA)
|
decreased neuronal migration
|
J:135408
|
Plxna3tm1Matl/Y
(either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1))
|
abnormal axon guidance
|
J:72426
|
abnormal axon pruning
|
J:83314
|
Plxna3tm1Matl/Y Plxna4tm1Matl/Plxna4tm1Matl
(either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1))
|
abnormal axon guidance
|
J:98440
|
Plxna3tm1Matl/Plxna3tm1Matl
(either: (involves: 129S1/Sv * C57BL/6) or (involves: 129S1/Sv * CD-1))
|
abnormal axon guidance
|
J:72426
|
abnormal axon pruning
|
J:83314
|
Plxna3tm1Matl/Plxna3tm1Matl Plxna4tm1Matl/Plxna4tm1Matl
(either: (involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6) or (involves: 129P2/OlaHsd * 129S1/Sv * CD-1))
|
abnormal axon guidance
|
J:98440
|
Plxna4tm1Hfu/Plxna4+
(B6.Cg-Plxna4tm1Hfu)
|
abnormal axon guidance
|
J:98330
|
Plxna4tm1Hfu/Plxna4tm1Hfu
(B6.Cg-Plxna4tm1Hfu)
|
abnormal axon guidance
|
J:98330
|
Plxna4tm1Hfu/Plxna4tm1Hfu
(involves: C57BL/6 * CBA)
|
abnormal neuron differentiation
|
J:135421
|
Plxna4tm1Matl/Plxna4tm1Matl
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * CD-1))
|
abnormal axon guidance
|
J:98440
|
Plxnb1tm1Matl/Plxnb1tm1Matl Plxnb2tm1c(EUCOMM)Wtsi/Plxnb2tm1Matl Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * C57BL/6N * SJL)
|
decreased neuronal precursor proliferation
|
J:228347
|
premature neuronal precursor differentiation
|
J:228347
|
Plxnb2tm1c(EUCOMM)Wtsi/Plxnb2tm1Matl Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * C57BL/6N * SJL)
|
abnormal neuronal precursor cell migration
|
J:228347
|
Plxnb2tm1Matl/Plxnb2tm1Matl
(involves: 129P2/OlaHsd * CD-1)
|
abnormal neuronal precursor cell migration
|
J:190014
|
abnormal radial glial cell morphology
|
J:119485
|
decreased neuronal precursor proliferation
|
J:190014
|
Plxnb2tm1Matl/Plxnb2tm1Matl
(B6.129P2-Plxnb2tm1Matl)
|
abnormal cerebellar granule cell migration
|
J:167973
|
Plxnb2tm1Matl/Plxnb2tm1Matl Sema4ctm1Matl/Sema4ctm1Matl
(B6.129P2-Sema4ctm1Matl Plxnb2tm1Matl)
|
abnormal cerebellar granule cell migration
|
J:167973
|
Plxnb2tm1Matl/Plxnb2tm1Matl Sema4gtm1Kik/Sema4gtm1Kik
(B6.Cg-Plxnb2tm1Matl Sema4gtm1Kik)
|
abnormal cerebellar granule cell migration
|
J:167973
|
Plxnc1tm1Alk/Plxnc1tm1Alk
(involves: 129/Sv * C57BL/6)
|
abnormal neuronal migration
|
J:120909
|
Plxnd1em1Zho/Plxnd1em1Zho
(C57BL/6-Plxnd1em1Zho)
|
abnormal vascular endothelial cell migration
|
J:326461
|
Plxnd1tm1.1Tmj/Plxnd1tm1.1Tmj Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S/SvEv * 129S4/SvJaeSor * C57BL/6 * CBA)
|
abnormal vascular endothelial cell migration
|
J:143763
|
Plxnd1tm1Joe/Plxnd1tm1Joe
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal vascular endothelial cell migration
|
J:143763
|
Pmaip1tm1Ast/Pmaip1tm1Ast
(C57BL/6-Pmaip1tm1Ast)
|
decreased sensitivity to induced cell death
|
J:86466
|
Pmaip1tm1Ttg/Pmaip1tm1Ttg
(B6.129P2-Pmaip1tm1Ttg)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:85569
|
decreased cellular sensitivity to X-ray irradiation
|
J:85569
|
decreased sensitivity to induced cell death
|
J:85569
|
Pmepa1em1Akt/Pmepa1em1Akt
(C57BL/6N-Pmepa1em1Akt)
|
abnormal osteoclast differentiation
|
J:329578
|
Pmfbp1em1Wli/Pmfbp1em1Wli
(involves: C57BL/6J * DBA/2J)
|
abnormal sperm axoneme morphology
|
J:266460
|
abnormal sperm connecting piece morphology
|
J:266460
|
absent sperm head
|
J:266460
|
Pmfbp1em#Jfw/Pmfbp1em#Jfw
(Not Specified)
|
abnormal sperm axoneme morphology
|
J:303070
|
absent sperm head
|
J:303070
|
disorganized sperm mitochondrial sheath
|
J:303070
|
Pmis2tm1Osb/Pmis2tm1Osb
(involves: 129 * C57BL/6)
|
impaired sperm migration in female genital tract
|
J:185714
|
Pmltm1.1Ews/Pmltm1.1Ews
(FVB.129P2-Pmltm1.1Ews)
|
abnormal double-strand DNA break repair
|
J:262172
|
abnormal PML bodies
|
J:262172
|
elevated level of mitotic sister chromatid exchange
|
J:262172
|
increased cellular sensitivity to ionizing radiation
|
J:262172
|
Pmltm1.1Ews/Pmltm1.1Ews Tg(PML-RARA)556Kog/0
(FVB.Cg-Pmltm1.1Ews Tg(PML-RARA)556Kog)
|
abnormal double-strand DNA break repair
|
J:262172
|
Pmltm1Ppp/Pmltm1Ppp
(involves: 129S7/SvEvBrd)
|
abnormal cell physiology
|
J:46381
|
increased fibroblast proliferation
|
J:46381
|
Pmltm1Ppp/Pmltm1Ppp
(FVB.129S7-Pmltm1Ppp)
|
abnormal double-strand DNA break repair
|
J:262172
|
Pmm2tm1.1Cknr/Pmm2tm2.1Cknr
(involves: C57BL/6J)
|
abnormal cell physiology
|
J:180794
|
Pmm2tm1Cthl/Pmm2tm1Cthl
(involves: 129P2/OlaHsd * C57BL/6)
|
maternal effect
|
J:111420
|
Pmp22tm1Ueli/Pmp22tm1Ueli
(involves: 129S/SvEv * C57BL/6)
|
increased Schwann cell proliferation
|
J:98118
|
Pmp22Tr-J/Pmp22+
(B6.Cg-Pmp22Tr-J Krt25Re/+ +/J)
|
abnormal autophagy
|
J:119095
|
abnormal cell physiology
|
J:97015
|
Pms2tm1.1Wed/Pms2tm1.1Wed
(involves: 129S6/SvEvTac * C57BL/6NCr)
|
abnormal DNA repair
|
J:162378
|
abnormal mismatch repair
|
J:162378
|
Pms2tm1Lisk/Pms2tm1Lisk
(involves: 129S2/SvPas * C57BL/6)
|
abnormal male meiosis
|
J:27389
|
abnormal mismatch repair
|
J:27389
|
abnormal sperm flagellum morphology
|
J:27389
|
globozoospermia
|
J:27389
|
oligozoospermia
|
J:27389
|
Pms2tm1Lisk/Pms2tm1Lisk
(involves: 129S2/SvPas)
|
abnormal cell physiology
|
J:125218
|
abnormal DNA repair
|
J:162378
|
abnormal mismatch repair
|
J:162378
|
abnormal sperm head morphology
|
J:162378
|
chromosomal instability
|
J:125218
|
coiled sperm flagellum
|
J:162378
|
decreased male germ cell number
|
J:162378
|
short sperm flagellum
|
J:162378
|
teratozoospermia
|
J:162378
|
Pms2tm1Lisk/Pms2tm1Lisk Terctm1Rdp/Terctm1Rdp
(involves: 129/Sv * 129S2/SvPas * C57BL/6 * C57BL/6J * SJL)
|
abnormal cell physiology
|
J:125218
|
abnormal DNA repair
|
J:125218
|
chromosomal instability
|
J:125218
|
decreased telomere length
|
J:125218
|
increased enterocyte apoptosis
|
J:125218
|
Pnkptm1.1Pmc/Pnkptm1.1Pmc Emx1tm1(cre)Krj/Emx1+
(involves: 129S1/Sv * 129S2/SvPas * C57BL/6)
|
decreased cell proliferation
|
J:226703
|
increased brain apoptosis
|
J:226703
|
Pnkptm1.1Pmc/Pnkptm1.1Pmc Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129S1/Sv * C57BL/6 * CBA)
|
increased brain apoptosis
|
J:226703
|
Pnkptm1.1Pmc/Pnkptm1.1Pmc Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * C57BL/6 * SJL)
|
abnormal DNA repair
|
J:226703
|
abnormal double-strand DNA break repair
|
J:226703
|
abnormal single-strand DNA break repair
|
J:226703
|
decreased cell proliferation
|
J:226703
|
increased brain apoptosis
|
J:226703
|
Pnkptm1Pmc/Pnkptm1Pmc
(involves: 129S1/Sv * C57BL/6)
|
abnormal DNA repair
|
J:226703
|
abnormal double-strand DNA break repair
|
J:226703
|
abnormal single-strand DNA break repair
|
J:226703
|
decreased cell proliferation
|
J:226703
|
increased brain apoptosis
|
J:226703
|
Pnldc1em1Nkn/Pnldc1em1Nkn
(involves: C57BL/6)
|
abnormal DNA methylation
|
J:262084
|
Pnldc1em2Nkn/Pnldc1em2Nkn
(involves: C57BL/6)
|
abnormal DNA methylation
|
J:262084
|
Pnpbata/Pnpbata
(C57BL/6JSfdAnu-Pnpbata)
|
decreased B cell proliferation
|
J:104190
|
Pnptm1Cmr/Pnptm1Cmr
(involves: 129)
|
abnormal DNA repair
|
J:62870
|
abnormal mitochondrial physiology
|
J:62870
|
increased cellular sensitivity to gamma-irradiation
|
J:62870
|
increased thymocyte apoptosis
|
J:62870
|
Pnpla2tm1.1Hsul/Pnpla2tm1.1Hsul Tg(Fabp4-cre)1Rev/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL)
|
decreased adipocyte glucose uptake
|
J:176083
|
decreased fatty acid oxidation
|
J:176083
|
Pnpla2tm1Gam/Pnpla2tm1Gam Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J * DBA)
|
decreased fatty acid oxidation
|
J:185116
|
Pnpla2tm1Rze/Pnpla2tm1Rze
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cardiomyocyte apoptosis
|
J:108546
|
Pnpla2tm1Rze/Pnpla2tm1Rze
(involves: 129P2/OlaHsd)
|
abnormal myocardial fiber mitochondrial morphology
|
J:176252
|
Pnpla6tm1Mos/Pnpla6tm1Mos
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased apoptosis
|
J:87675
|
increased placenta apoptosis
|
J:87675
|
Pnpla8tm1Rigr/Pnpla8tm1Rigr
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal aerobic respiration
|
J:128989
|
abnormal mitochondrial physiology
|
J:128989
|
Pnpt1tm1.1Teit/Pnpt1tm1.1Teit
(involves: C57BL/6)
|
abnormal mitochondrial physiology
|
J:167932
|
Pnpt1tm1Teit/Pnpt1tm1Teit Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:167932
|
abnormal mitochondrial crista morphology
|
J:167932
|
abnormal mitochondrial physiology
|
J:167932
|
Poc1acha/Poc1acha
(involves: DBA/2J)
|
azoospermia
|
J:90436
|
Poc1bem1Xjzha/Poc1bem1Xjzha
(C57BL/6J-Poc1bem1Xjzha)
|
abnormal acrosome morphology
|
J:340269
|
abnormal outer dense fiber morphology
|
J:340269
|
abnormal sperm end piece morphology
|
J:340269
|
abnormal sperm flagellum morphology
|
J:340269
|
abnormal sperm head morphology
|
J:340269
|
abnormal sperm midpiece morphology
|
J:340269
|
abnormal spermatid morphology
|
J:340269
|
absent sperm axonemal central pair
|
J:340269
|
decreased elongated spermatid number
|
J:340269
|
immotile sperm
|
J:340269
|
oligozoospermia
|
J:340269
|
short sperm flagellum
|
J:340269
|
teratozoospermia
|
J:340269
|
Podxltm2Kmn/Podxltm2Kmn Tg(Cdh5-cre)7Mlia/0
(B6.Cg-Podxltm2Kmn Tg(Cdh5-cre)7Mlia)
|
decreased lung endothelial cell adhesion
|
J:223453
|
increased lung endothelial cell adhesion
|
J:223453
|
Pofut2Gt(RST434)Byg/Pofut2Gt(RST434)Byg
(involves: 129P2/OlaHsd)
|
abnormal vascular endothelial cell differentiation
|
J:165751
|
Polbtm1.1Jbsw/Polbtm1.1Jbsw
(involves: 129/Sv * C57BL/6)
|
abnormal base-excision repair
|
J:183837
|
abnormal cell cycle
|
J:183837
|
chromosomal instability
|
J:183837
|
decreased cell proliferation
|
J:183837
|
decreased fibroblast proliferation
|
J:183837
|
increased embryonic tissue cell apoptosis
|
J:183837
|
increased hepatocyte apoptosis
|
J:183837
|
increased kidney apoptosis
|
J:183837
|
increased neuron apoptosis
|
J:183837
|
increased sensitivity to induced cell death
|
J:183837
|
increased splenocyte apoptosis
|
J:183837,
J:206872
|
Polbtm1Koy/Polbtm1Koy
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuron differentiation
|
J:61143
|
increased neuron apoptosis
|
J:61143
|
Pold1tm1Uchi/Pold1tm1Uchi
(C57BL/6-Pold1tm1Uchi)
|
absent inner cell mass proliferation
|
J:144992
|
Pold1tyrn/Pold1tyrn
(C57BL/6J-Pold1tyrn)
|
decreased cell proliferation
|
J:327432
|
increased embryonic tissue cell apoptosis
|
J:327432
|
Pold3em1Linl/Pold3+
(involves: C57BL/6 * DBA/2)
|
abnormal double-strand DNA break repair
|
J:263620
|
arrest of male meiosis
|
J:263620
|
decreased male germ cell number
|
J:263620
|
decreased telomere length
|
J:263620
|
increased male germ cell apoptosis
|
J:263620
|
spontaneous chromosome breakage
|
J:263620
|
Pold3em1Linl/Pold3em1Linl
(involves: C57BL/6 * DBA/2)
|
abnormal trophoblast giant cell proliferation
|
J:263620
|
decreased inner cell mass proliferation
|
J:263620
|
Pole3em3Tbo/Pole3em3Tbo
(FVB-Pole3em3Tbo)
|
abnormal cell cycle
|
J:298827
|
abnormal thymus apoptosis
|
J:298827
|
increased thymocyte apoptosis
|
J:298827
|
Pole3em4Tbo/Pole3em4Tbo
(FVB-Pole3em4Tbo)
|
abnormal thymus apoptosis
|
J:298827
|
increased thymocyte apoptosis
|
J:298827
|
Pole4tm1(KOMP)Vlcg/Pole4tm1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
abnormal DNA replication
|
J:261973
|
Pole4tm1(KOMP)Vlcg/Pole4tm1(KOMP)Vlcg
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6NTac * FVB/N)
|
abnormal cell cycle
|
J:261973
|
abnormal DNA replication
|
J:261973
|
chromosomal instability
|
J:261973
|
decreased fibroblast proliferation
|
J:261973
|
decreased male germ cell number
|
J:261973
|
increased cellular sensitivity to hydroxyurea
|
J:261973
|
increased embryonic tissue cell apoptosis
|
J:261973
|
increased forebrain apoptosis
|
J:261973
|
induced chromosome breakage
|
J:261973
|
Polg2tm1.1Wcc/Polg2tm1.1Wcc
(involves: C57BL/6 * CBA)
|
abnormal mitochondrial morphology
|
J:192568
|
abnormal respiratory electron transport chain
|
J:192568
|
decreased mitochondrial DNA content
|
J:192568
|
disorganized mitochondrial cristae
|
J:192568
|
Polgtm1.1Lrsn/Polgtm1.1Lrsn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:91077
|
azoospermia
|
J:91077
|
increased mitochondrial size
|
J:91077
|
oligozoospermia
|
J:91077
|
Polgtm1Jiha/Polg+
(involves: C57BL/6JJcl)
|
abnormal oxidative phosphorylation
|
J:199416
|
oxidative stress
|
J:199416
|
Polgtm1Jiha/Polgtm1Jiha
(involves: C57BL/6JJcl)
|
abnormal oxidative phosphorylation
|
J:199416
|
Polgtm1Prol/Polgtm1Prol
(involves: 129S7/SvEvBrd * C57BL/6J * ICR)
|
abnormal mitochondrial physiology
|
J:119971
|
increased apoptosis
|
J:99764
|
Polgtm1Prol/Polgtm1Prol
(B6J.129S7-Polgtm1Prol)
|
abnormal mitochondrial physiology
|
J:154187
|
Polktm1.1Rsky/Polktm1.1Rsky
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6)
|
abnormal DNA repair
|
J:112191
|
increased cellular sensitivity to ultraviolet irradiation
|
J:80212
|
Polltm1Crey/Polltm1Crey
(involves: 129P2/OlaHsd)
|
abnormal base-excision repair
|
J:99087
|
Polmtm1Crey/Polmtm1Crey
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal B cell proliferation
|
J:85190
|
Polntm1.2Rwd/Polntm1.2Rwd
(involves: 129 * C57BL/6J * DBA/2J)
|
abnormal meiosis
|
J:241704
|
Polntm1.2Rwd/Polntm1.2Rwd Polqtm1Jcs/Polqtm1Jcs
(involves: 129S4/SvJae * C57BL/6J)
|
increased cellular sensitivity to gamma-irradiation
|
J:241704
|
Polqchaos1/Polqchaos1
(involves: C3HeB/FeJ * C57BL/6J)
|
chromosome breakage
|
J:82700
|
Polr1bGt(Ayu8019)Imeg/Polr1bGt(Ayu8019)Imeg
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal nucleolus morphology
|
J:130226
|
Polr1dem1(IMPC)J/Polr1dem1(IMPC)J
(C57BL/6NJ-Polr1dem1(IMPC)J/Mmjax)
|
increased embryonic tissue cell apoptosis
|
J:299155
|
Polr2mtm1.1Rgr/Polr2mtm1.1Rgr Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA)
|
increased hepatocyte karyomegaly
|
J:291184
|
Polr2mtm1.1Rgr/Polr2mtm1.1Rgr Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6 * DBA)
|
increased hepatocyte apoptosis
|
J:291184
|
increased hepatocyte proliferation
|
J:291184
|
Polrmttm1.1Arte/Polrmttm1.1Arte Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6N * FVB)
|
abnormal mitochondrial morphology
|
J:258184
|
abnormal mitochondrial physiology
|
J:258184
|
Polrmttm1.2Arte/Polrmt+ Tefmtm1.2Lrsn/Tefm+
(involves: C57BL/6N)
|
cellular phenotype
|
J:276874
|
Pomctm1Low/Pomctm1Low
(involves: 129S2/SvPas * C57BL/6)
|
increased splenocyte proliferation
|
J:102955
|
Pomgnt1Gt(OST179231)Lex/Pomgnt1Gt(OST179231)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal basement membrane morphology
|
J:196379
|
impaired basement membrane formation
|
J:196379
|
Pomgnt1tm1.1Cfg/Pomgnt1tm1.1Cfg
(involves: C57BL/6)
|
abnormal radial glial cell morphology
|
J:258757
|
Pomgnt1tm1Stk/Pomgnt1tm1Stk
(involves: 129S/SvEv)
|
abnormal skeletal muscle satellite cell proliferation
|
J:144928
|
Pomgnt2tm1Kkat/Pomgnt2tm1Kkat
(either: B6J.Cg-Pomgnt2tm1Kkat or (involves: C57BL/6J * C57BL/6NJcl) or (involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj))
|
abnormal basal lamina morphology
|
J:215959
|
abnormal neuronal migration
|
J:215959
|
radial glial endfoot detachment
|
J:215959
|
PomkGt(OST243203)Lex/PomkGt(OST243203)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal cerebellar granule cell migration
|
J:185566
|
abnormal neuronal migration
|
J:185566
|
abnormal Purkinje cell migration
|
J:185566
|
Pomt2tm1.1Hhu/Pomt2tm1.1Hhu Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J)
|
abnormal basement membrane morphology
|
J:179356
|
abnormal radial glial cell morphology
|
J:179356
|
Pomt2tm1.1Hhu/Pomt2tm1.1Hhu Tg(GFAP-cre)25Mes/0
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J * FVB/N)
|
abnormal basement membrane morphology
|
J:179356
|
abnormal cerebellar granule cell migration
|
J:179356
|
Pomt2tm1Sstr/Pomt2tm1Sstr
(involves: 129P2/OlaHsd)
|
abnormal cell adhesion
|
J:205502
|
Pon1tm1Lus/Pon1tm1Lus
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:82696
|
Pon2Gt(XE661)Byg/Pon2Gt(XE661)Byg
(B6.129P2-Pon2Gt(XE661)Byg)
|
abnormal macrophage chemotaxis
|
J:116935
|
oxidative stress
|
J:116935
|
Pon3tm1Dmsh/Pon3tm1Dmsh
(B6J.129X1-Pon3tm1Dmsh)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:234615
|
decreased fatty acid oxidation
|
J:234615
|
increased hepatocyte apoptosis
|
J:234615
|
oxidative stress
|
J:234615
|
Pon3tm1Lus/Pon3tm1Lus
(involves: 129X1/SvJ)
|
oxidative stress
|
J:204799
|
Poo/Poo
(involves: C57BL/Ws * LT/SvKau)
|
abnormal meiosis
|
J:17685
|
PopoaLT/SvKau/?
(involves: CAST/Ei * LT/SvKau)
|
abnormal female meiosis
|
J:93219
|
Portm1Cbk/Portm1Cbk
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell adhesion
|
J:74666
|
increased apoptosis
|
J:74666
|
Postntm1Jmol/Postntm1Jmol
(involves: 129/Sv * C57BL/6)
|
abnormal cell adhesion
|
J:140301
|
Pot1atm1.1Schg/Pot1atm1.1Schg
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased cell proliferation
|
J:112184
|
Pot1atm1Schg/Pot1atm1.1Schg
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal chromosome morphology
|
J:112184
|
abnormal telomere length
|
J:112184
|
decreased cell proliferation
|
J:112184
|
Pot1atm1Schg/Pot1atm1.1Schg Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * 129S7/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:112184
|
abnormal chromosome morphology
|
J:112184
|
cellular phenotype
|
J:112184
|
chromosome breakage
|
J:112184
|
elevated level of mitotic sister chromatid exchange
|
J:112184
|
Pot1btm1.1Schg/Pot1btm1.1Schg
(involves: 129S6/SvEvTac * C57BL/6)
|
increased male germ cell apoptosis
|
J:144553
|
Pot1btm1.1Schg/Pot1btm1.1Schg
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL)
|
decreased male germ cell number
|
J:144553
|
Pot1btm1.1Schg/Pot1btm1.1Schg Terctm1Rdp/Terc+
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL)
|
decreased male germ cell number
|
J:144553
|
increased apoptosis
|
J:144553
|
Pot1btm1.1Schg/Pot1btm1.1Schg Terctm1Rdp/Terctm1Rdp
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL)
|
decreased male germ cell number
|
J:144553
|
Pou1f1dw/Pou1f1dw
(Not Specified)
|
abnormal actin cytoskeleton morphology
|
J:144823
|
Pou1f1dw/Pou1f1dw
(DW/J Pou1f1dw)
|
increased pituitary gland apoptosis
|
J:108961
|
Pou2af1tm1Pjln/Pou2af1tm1Pjln
(involves: C57BL/6)
|
increased B cell apoptosis
|
J:67362
|
Pou2af1tm1Rgr/Pou2af1tm1Rgr
(either: (involves: 129P2/OlaHsd) or (involves: 129S1/Sv))
|
decreased B cell proliferation
|
J:35785
|
increased B cell proliferation
|
J:114816
|
Pou2af2em1Crva/Pou2af2em1Crva
(C57BL/6-Pou2af2em1Crva)
|
abnormal gastrointestinal brush cell morphology
|
J:325394
|
abnormal respiratory tract brush cell morphology
|
J:325394
|
Pou2f3tm1Rsd/Pou2f3tm1Rsd
(involves: 129/Sv * 129S4/SvJae * C57BL/6J)
|
abnormal keratinocyte differentiation
|
J:42016
|
Pou3f2tm1Tno/Pou3f2tm1Tno Pou3f3tm1Tno/Pou3f3tm1Tno
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal neuronal migration
|
J:77999
|
Pou3f3tm1Tno/Pou3f3tm1Tno
(involves: 129S4/SvJae * C57BL/6J)
|
decreased kidney cell proliferation
|
J:84756
|
increased kidney apoptosis
|
J:84756
|
Pou4f2tm1(ALPP)Whk/Pou4f2tm2Whk
(Not Specified)
|
increased retina apoptosis
|
J:96926
|
Pou4f3tm1Rsd/Pou4f3tm1Rsd
(involves: 129S4/SvJae * C57BL/6)
|
abnormal organ of Corti supporting cell differentiation
|
J:57149
|
Pou4f3tm1Xia/Pou4f3tm1Xia
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal pillar cell differentiation
|
J:82156
|
Pparatm1Gonz/Pparatm1Gonz
(involves: C57BL/6)
|
abnormal keratinocyte differentiation
|
J:64345
|
Pparatm1Gonz/Pparatm1Gonz
(involves: 129S4/SvJae)
|
decreased fatty acid oxidation
|
J:176083
|
Pparatm1Gonz/Pparatm1Gonz
(involves: 129S4/SvJae * C57BL/6J)
|
increased muscle cell glucose uptake
|
J:129848
|
Ppardtm1Dsvg/Ppardtm1Dsvg
(involves: 129S2/SvPas * C57BL/6)
|
impaired osteoblast differentiation
|
J:219677
|
Ppardtm1Wwah/Ppard+
(Not Specified)
|
abnormal keratinocyte adhesion
|
J:71272
|
increased keratinocyte proliferation
|
J:71272
|
Ppardtm1Wwah/Ppardtm1Wwah
(Not Specified)
|
decreased keratinocyte proliferation
|
J:96826
|
increased keratinocyte apoptosis
|
J:96826
|
Ppargtm1.1Auw/Ppargtm1.1Auw
(B6.Cg-Ppargtm1.1Auw)
|
abnormal cell differentiation
|
J:144344
|
increased adipocyte glucose uptake
|
J:144344
|
Ppargtm1.1Gonz/Ppargtm1.1Gonz Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6)
|
impaired macrophage phagocytosis
|
J:168799
|
increased mesangial cell number
|
J:168799
|
increased renal glomerulus apoptosis
|
J:168799
|
Ppargtm1Avp/Pparg+
(involves: 129S2/SvPas * C57BL/6)
|
abnormal fat cell differentiation
|
J:116568
|
Ppargtm1Lja/Pparg+
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased skeletal muscle cell glucose uptake
|
J:98786
|
Ppargtm1Rev/Ppargtm1Rev
(involves: 129S4/SvJae)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:58223
|
Ppargtm1Tka/Pparg+
(involves: C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:58222
|
abnormal osteoblast differentiation
|
J:89250
|
Ppargtm1Tka/Pparg+
(involves: C57BL/6 * CBA * ICR)
|
increased B cell proliferation
|
J:58222
|
Ppargtm1Tka/Ppargtm1Tka
(involves: C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:58222,
J:89250
|
Ppargtm2Rev/Ppargtm2Rev Tg(Tek-cre)1Ywa/?
(involves: 129S4/SvJae * C57BL/6 * SJL)
|
abnormal osteoclast differentiation
|
J:160910
|
Ppargc1atm1Brsp/Ppargc1a+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal mitochondrial physiology
|
J:264271
|
decreased mitochondrial DNA content
|
J:264271
|
impaired autophagy
|
J:264271
|
oxidative stress
|
J:264271
|
Ppargc1atm1Brsp/Ppargc1atm1Brsp
(involves: 129/Sv * C57BL/6 * FVB/N)
|
abnormal cellular respiration
|
J:93896
|
Ppargc1atm1Brsp/Ppargc1atm2Brsp Tg(Myog-cre)1Eno/0
(involves: 129 * C57BL/6 * FVB/N)
|
abnormal mitochondrial physiology
|
J:127403
|
Ppargc1atm1Dpk/Ppargc1atm1Dpk
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cellular respiration
|
J:96306
|
Ppargc1atm2.1Brsp/Ppargc1atm2.1Brsp Tg(Myog-cre)1Eno/0
(involves: 129 * BALB/c * C57BL/6J * C57BL/6N)
|
abnormal mitochondrial physiology
|
J:208380
|
Ppargc1atm2Brsp/Ppargc1atm2Brsp Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129 * C57BL/6 * DBA)
|
abnormal cell physiology
|
J:115197
|
Ppargc1btm1.1Avp/Ppargc1btm1.1Avp
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6)
|
abnormal myocardial fiber mitochondrial morphology
|
J:116167
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:116167
|
Ppargc1btm1.1Javi/Ppargc1btm1.1Javi Tg(Fabp4-cre)1Rev/?
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal mitochondrial physiology
|
J:221221
|
abnormal oxidative phosphorylation
|
J:221221
|
abnormal respiratory electron transport chain
|
J:221221
|
abnormal tricarboxylic acid cycle
|
J:221221
|
Ppargc1btm1.2Rev/Ppargc1btm1.2Rev Tg(Tek-cre)1Ywa/0
(involves: 129/Sv * C57BL/6 * C57BL/6J * SJL)
|
abnormal osteoclast differentiation
|
J:160910
|
Ppargc1btm1Lowl/Ppargc1btm1Lowl
(involves: C57BL/6)
|
abnormal mitochondrial morphology
|
J:129775
|
abnormal mitochondrial physiology
|
J:129775
|
Ppbptm1(KOMP)Vlcg/Ppbptm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal leukocyte migration
|
J:198197
|
Ppfia3em1Pska/Ppfia3em1Pska
(129S2.FVB-Ppfia3em1Pska)
|
abnormal synaptic vesicle exocytosis
|
J:265782
|
Ppidem1Cask/Ppidem1Cask
(Not Specified)
|
abnormal mitochondrial physiology
|
J:358023
|
Ppiftm1.1Mmos/Ppiftm1.1Mmos
(involves: 129X1/SvJ * FVB/NJ)
|
abnormal mitochondrial physiology
|
J:101149
|
Ppiftm1Jmol/Ppiftm1Jmol
(involves: 129)
|
abnormal mitochondrial physiology
|
J:97660
|
Ppiftm1Maf/Ppiftm1Maf
(B6.129-Ppiftm1Maf)
|
abnormal mitochondrial physiology
|
J:99922
|
Ppiftm1Tsu/Ppiftm1Tsu
(involves: 129S5/SvEvBrd)
|
abnormal mitochondrial physiology
|
J:97673
|
decreased cellular sensitivity to hydrogen peroxide
|
J:97673
|
decreased sensitivity to induced cell death
|
J:157346
|
Ppil1em3Jgg/Ppil1em3Jgg
(C57BL/6-Ppil1em3Jgg)
|
increased neuron apoptosis
|
J:300487
|
Ppil1em4Jgg/Ppil1em4Jgg
(C57BL/6-Ppil1em4Jgg)
|
increased neuron apoptosis
|
J:300487
|
Ppm1atm1.1Xya/Ppm1atm1.1Xya
(involves: 129S6/SvEvTac * FVB/N)
|
decreased keratinocyte migration
|
J:178733
|
Ppm1atm1.1Xya/Ppm1atm1.1Xya Smad2tm1Xya/Smad2tm1Xya Tg(KRT5-cre)1Xya/0
(involves: 129S6/SvEvTac * FVB/N)
|
increased keratinocyte migration
|
J:178733
|
Ppm1atm1Xya/Ppm1atm1Xya Tg(KRT5-cre)1Xya/0
(involves: 129S6/SvEvTac)
|
decreased keratinocyte migration
|
J:178733
|
Ppm1bGt(AW0406)Wtsi/Ppm1bGt(AW0406)Wtsi
(B6.129P2-Ppm1bGt(AW0406)Wtsi)
|
abnormal cell death
|
J:243815
|
Ppm1bGt(AW0406)Wtsi/Ppm1bGt(AW0406)Wtsi Ripk3tm1Vmd/Ripk3tm1Vmd
(B6.129-Ripk3tm1Vmd Ppm1bGt(AW0406)Wtsi)
|
cellular phenotype
|
J:243815
|
Ppm1dtm1Lad/Ppm1dtm1Lad
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased B cell proliferation
|
J:74284
|
decreased T cell proliferation
|
J:74284
|
oligozoospermia
|
J:74284
|
Ppm1dtm1Lad/Ppm1dtm1Lad
(involves: 129S7/SvEvBrd)
|
decreased pancreatic beta cell proliferation
|
J:151980
|
Ppm1ktm1Yiwa/Ppm1ktm1Yiwa
(involves: 129/Sv * C57BL/6)
|
oxidative stress
|
J:150451
|
Ppp1cctm1Lex/Ppp1cctm1Lex Tg(Stra8-icre)1Reb/0
(involves: 129S/SvEvBrd * FVB/NJ)
|
abnormal sperm mitochondrial sheath morphology
|
J:203985
|
asthenozoospermia
|
J:203985
|
kinked sperm flagellum
|
J:203985
|
oligozoospermia
|
J:203985
|
teratozoospermia
|
J:203985
|
Ppp1cctm1Var/Ppp1cctm1Var
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal male meiosis
|
J:52211
|
decreased male germ cell number
|
J:52211
|
oligozoospermia
|
J:52211
|
Ppp1cctm1Var/Ppp1cctm1Var
(involves: CD-1)
|
abnormal outer dense fiber morphology
|
J:122018
|
abnormal sperm fibrous sheath morphology
|
J:122018
|
abnormal sperm flagellum morphology
|
J:122018
|
abnormal sperm head morphology
|
J:122018,
J:82546
|
abnormal sperm midpiece morphology
|
J:122018
|
abnormal sperm principal piece morphology
|
J:122018
|
absent sperm mitochondrial sheath
|
J:122018
|
decreased elongated spermatid number
|
J:122018
|
disorganized sperm mitochondrial sheath
|
J:122018
|
globozoospermia
|
J:122018
|
multiflagellated sperm
|
J:82546
|
oligozoospermia
|
J:122018,
J:82546
|
pinhead sperm
|
J:122018
|
Ppp1r3atm1Ptwc/Ppp1r3atm1Ptwc
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased skeletal muscle cell glucose uptake
|
J:82422
|
Ppp1r3ctm1Adpr/Ppp1r3ctm1Adpr
(B6.Cg-Ppp1r3ctm1Adpr)
|
increased muscle cell glucose uptake
|
J:242758
|
Ppp1r3ctm1Ars/Ppp1r3c+
(B6.129-Ppp1r3ctm1Ars)
|
decreased skeletal muscle cell glucose uptake
|
J:83297
|
Ppp1r9btm1Jfe/Ppp1r9btm1Jfe
(involves: 129X1/SvJ * C57BL/6)
|
decreased susceptibility to neuronal excitotoxicity
|
J:77284
|
Ppp1r13ltm1.1Xlu/Ppp1r13l+
(involves: 129 * BALB/cJ * C57BL/6J)
|
decreased fibroblast proliferation
|
J:177360
|
Ppp1r13ltm1.1Xlu/Ppp1r13ltm1.1Xlu
(involves: 129 * BALB/cJ * C57BL/6J)
|
abnormal cell morphology
|
J:177360
|
decreased fibroblast proliferation
|
J:177360
|
decreased keratinocyte proliferation
|
J:177360
|
early cellular replicative senescence
|
J:177360
|
Ppp1r15atm1Dron/Ppp1r15atm1Dron
(involves: 129S6/SvEvTac)
|
abnormal cell physiology
|
J:82255
|
Ppp1r15atm1Kii/Ppp1r15atm1Kii
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:110590
|
Ppp1r18em1Mgin/Ppp1r18em1Mgin
(B6J.B6N-Ppp1r18em1Mgin)
|
impaired leukocyte migration
|
J:331428
|
Ppp1r18em3Mgin/Ppp1r18em3Mgin
(B6J.B6N-Ppp1r18em3Mgin)
|
impaired leukocyte migration
|
J:331428
|
Ppp1r35tm1.1(KOMP)Vlcg/Ppp1r35tm1.1(KOMP)Vlcg
(B6N(Cg)-Ppp1r35tm1.1(KOMP)Vlcg/J)
|
abnormal cell cycle
|
J:290235
|
absent embryonic cilia
|
J:290235
|
decreased embryonic neuroepithelium primary cilium number
|
J:290235
|
increased neural tube apoptosis
|
J:279207,
J:290235
|
Ppp2catm1.1Jmli/Ppp2catm1.2Jmli Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6J * FVB)
|
arrest of male meiosis
|
J:222054
|
Ppp2r1btm1.2Yxy/Ppp2r1btm1.2Yxy
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal male meiosis
|
J:308739
|
arrest of male meiosis
|
J:308739
|
azoospermia
|
J:308739
|
increased male germ cell apoptosis
|
J:308739
|
Ppp2r3ctm1Imku/Ppp2r3ctm1Imku Tg(CD19-cre/ERT2)1Cgn/?
(involves: C57BL/6)
|
decreased B cell proliferation
|
J:100706
|
Ppp2r5cGt(XP0444)Wtsi/Ppp2r5cGt(XP0444)Wtsi
(B6.129P2-Ppp2r5cGt(XP0444)Wtsi)
|
increased fetal cardiomyocyte apoptosis
|
J:210365
|
Ppp3catm1Jse/Ppp3catm1Jse
(either: (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6))
|
decreased T cell proliferation
|
J:71750
|
Ppp3cbM1Btlr/Ppp3cb+
(C57BL/6J-Ppp3cbM1Btlr)
|
increased CD8-positive, alpha-beta memory T cell proliferation
|
J:236670
|
Ppp3cbM1Btlr/Ppp3cbM1Btlr
(C57BL/6J-Ppp3cbM1Btlr)
|
increased CD8-positive, alpha-beta memory T cell proliferation
|
J:236670
|
Ppp3cbm2Btlr/Ppp3cb+
(C57BL/6J-Ppp3cbm2Btlr)
|
increased CD8-positive, alpha-beta memory T cell proliferation
|
J:236671
|
Ppp3cbm2Btlr/Ppp3cbm2Btlr
(C57BL/6J-Ppp3cbm2Btlr)
|
increased CD8-positive, alpha-beta memory T cell proliferation
|
J:236671
|
Ppp3cbtm1Jmk/Ppp3cbtm1Jmk
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased T cell proliferation
|
J:77729
|
Ppp3cbtm1Jmk/Ppp3cbtm1Jmk
(involves: 129S6/SvEvTac)
|
decreased T cell proliferation
|
J:109586
|
Ppp3cctm1.1Osb/Ppp3cctm1.1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal sperm midpiece morphology
|
J:226539
|
decreased hyperactivated sperm motility
|
J:226539
|
Ppp3r1tm1.1Jhon/Ppp3r1tm1.1Jhon
(involves: C57BL/6 * C57BL/6NTac)
|
cardiac interstitial fibrosis
|
J:298603
|
increased cardiomyocyte apoptosis
|
J:298603
|
Ppp3r1tm2Grc/Ppp3r1tm2.1Grc Tg(Pax3-cre)1Joe/0
(involves: 129S6/SvEvTac)
|
decreased cell proliferation
|
J:89217
|
Ppp3r1tm2Grc/Ppp3r1tm2Grc Tg(Pax3-cre)1Joe/0
(involves: 129S6/SvEvTac)
|
decreased cell proliferation
|
J:89217
|
Ppp3r2em1Osb/Ppp3r2em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm midpiece morphology
|
J:226539
|
decreased hyperactivated sperm motility
|
J:226539
|
Ppp4cem1Qys/Ppp4cem1Qys Tg(Stra8-icre)1Reb/0
(involves: 129S/SvEv * C57BL/6 * FVB/NJ)
|
abnormal sperm midpiece morphology
|
J:309155
|
abnormal spermatocyte morphology
|
J:309155
|
asthenozoospermia
|
J:309155
|
decreased sperm progressive motility
|
J:309155
|
increased male germ cell apoptosis
|
J:309155
|
kinked sperm flagellum
|
J:309155
|
oligozoospermia
|
J:309155
|
Ppp4ctm1.1Htn/Ppp4ctm1.1Htn
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal cell cycle
|
J:134682
|
abnormal microtubule cytoskeleton morphology
|
J:134682
|
Ppp5cGt(XG029)Byg/Ppp5cGt(XG029)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle checkpoint function
|
J:122564
|
Ppp5ctm1.2Rhon/Ppp5ctm1.2Rhon
(B6.129X1-Ppp5ctm1.2Rhon)
|
abnormal cell adhesion
|
J:178164
|
abnormal cell morphology
|
J:178164
|
decreased fibroblast proliferation
|
J:178164
|
Ppt2tm1Hof/Ppt2tm1Hof
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased neuron apoptosis
|
J:86202
|
Pptc7em1Pagd/Pptc7em1Pagd
(C57BL/6J-Pptc7em1Pagd)
|
abnormal hepatocyte mitochondrial morphology
|
J:277086
|
abnormal mitochondrial biogenesis
|
J:277086
|
abnormal mitochondrial physiology
|
J:277086
|
abnormal myocardial fiber mitochondrial morphology
|
J:277086
|
Pptc7em2Pagd/Pptc7em2Pagd
(C57BL/6J-Pptc7em2Pagd)
|
abnormal hepatocyte mitochondrial morphology
|
J:277086
|
abnormal mitochondrial biogenesis
|
J:277086
|
abnormal mitochondrial physiology
|
J:277086
|
abnormal myocardial fiber mitochondrial morphology
|
J:277086
|
Pqbp1tm1.1Hiok/Y Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J)
|
abnormal cell cycle
|
J:279053
|
abnormal cell cycle checkpoint function
|
J:279053
|
abnormal mitosis
|
J:279053
|
Pramel1em1Liuw/Pramel1em1Liuw
(involves: C57BL/6)
|
abnormal male germ cell morphology
|
J:342835
|
abnormal spermatogonia morphology
|
J:342835
|
abnormal spermatogonia proliferation
|
J:342835
|
decreased male germ cell apoptosis
|
J:342835
|
decreased male germ cell number
|
J:342835
|
decreased spermatogonia number
|
J:342835
|
increased male germ cell apoptosis
|
J:342835
|
oligozoospermia
|
J:342835
|
Pramel1em1Liuw/Pramel1em1Liuw Tg(Id4-EGFP)LT-11B6Oat/0
(involves: C57BL/6 * FVB)
|
abnormal spermatogonia morphology
|
J:342835
|
Pramel1em2Liuw/Pramel1em2Liuw Tg(Stra8-icre)1Reb/0
(involves: C57BL/6 * FVB/NJ)
|
oligozoospermia
|
J:342835
|
Pramel13em2Dean/Pramel13em2Dean
(involves: C57BL/6J * DBA/2J)
|
abnormal spermatogonia proliferation
|
J:282232
|
azoospermia
|
J:282232
|
increased male germ cell apoptosis
|
J:282232
|
Pramel15em1Bzhu/Pramel15em1Bzhu
(C57BL/6J-Pramel15em1Bzhu)
|
abnormal DNA methylation
|
J:354132
|
Pramel15em2Bzhu/Pramel15em2Bzhu
(C57BL/6J-Pramel15em2Bzhu)
|
abnormal DNA methylation
|
J:354132
|
Pramex1tm1c(KOMP)Wtsi/Y Tg(Stra8-icre)1Reb/0
(involves: C57BL/6J * C57BL/6N)
|
abnormal spermatocyte morphology
|
J:290700
|
decreased male germ cell number
|
J:290700
|
increased male germ cell apoptosis
|
J:290700
|
increased testis apoptosis
|
J:290700
|
oligozoospermia
|
J:290700
|
Prap1tm1Lex/Prap1tm1Lex
(B6.129S5-Prap1tm1Lex)
|
abnormal cell cycle
|
J:304152
|
increased cellular sensitivity to ionizing radiation
|
J:304152
|
increased enterocyte apoptosis
|
J:304152
|
Prdm1tm1.1Clme/Prdm1+
(involves: 129S1/Sv * 129X1/SvJ * FVB/N * ICR)
|
decreased primordial germ cell number
|
J:101718
|
Prdm1tm1.1Clme/Prdm1tm1.1Clme
(involves: 129S1/Sv * 129X1/SvJ * FVB/N * ICR)
|
decreased primordial germ cell number
|
J:101718
|
Prdm1tm1.1Clme/Prdm1tm1.1Liz
(involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ)
|
abnormal germ cell morphology
|
J:153979
|
absent oocytes
|
J:153979
|
azoospermia
|
J:153979
|
decreased primordial germ cell number
|
J:153979
|
Prdm1tm1.1Clme/Prdm1tm2Rob
(involves: 129S/Sv * 129X1/Sv * C57BL/6 * FVB/N * ICR)
|
absent primordial germ cells
|
J:101718
|
Prdm1tm1Clme/Prdm1tm1Clme Tg(Itgax-cre)1-1Reiz/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA)
|
abnormal mesangial cell morphology
|
J:178876
|
Prdm1tm1Masu/Prdm1+
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased primordial germ cell number
|
J:99994
|
Prdm1tm1Masu/Prdm1tm1Masu
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal primordial germ cell migration
|
J:99994
|
decreased primordial germ cell number
|
J:99994
|
Prdm1tm1Rob/Prdm1+
(involves: 129S/SvEv * C57BL/6)
|
decreased primordial germ cell number
|
J:101718
|
Prdm1tm1Rob/Prdm1tm1Rob
(involves: 129S/SvEv * C57BL/6)
|
decreased primordial germ cell number
|
J:101718
|
Prdm1tm2Rob/Prdm1+
(involves: 129S/SvEv * C57BL/6)
|
decreased primordial germ cell number
|
J:101718
|
Prdm1tm2Rob/Prdm1tm2Rob
(involves: 129S/SvEv * C57BL/6)
|
decreased primordial germ cell number
|
J:101718
|
Prdm8tm1Mci/Prdm8tm1Mci
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal axon guidance
|
J:182304
|
Prdm9em2Kpgn/Prdm9+
(C57BL/6J-Prdm9em2Kpgn/Kpgn)
|
decreased oocyte number
|
J:299008
|
Prdm9em2Kpgn/Prdm9em2Kpgn
(C57BL/6J-Prdm9em2Kpgn/Kpgn)
|
abnormal chiasmata formation
|
J:299008
|
abnormal chromosomal synapsis
|
J:299008
|
abnormal DNA methylation during gametogenesis
|
J:299008
|
abnormal female meiosis
|
J:299008
|
arrest of male meiosis
|
J:299008
|
decreased oocyte number
|
J:299008
|
Prdm9em3Kpgn/Prdm9em3Kpgn
(involves: C57BL/6J)
|
cellular phenotype
|
J:280261
|
Prdm9em3Kpgn/Prdm9em3Kpgn Stag3tm1e.1(KOMP)Wtsi/Stag3tm1e.1(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal double-strand DNA break repair
|
J:280261
|
Prdm9M1045Lja/Prdm9+
(involves: C57BL/6J * DBA)
|
azoospermia
|
J:179895
|
decreased elongated spermatid number
|
J:179895
|
decreased male germ cell number
|
J:179895
|
Prdm9M1045Lja/Prdm9M1045Lja
(involves: C57BL/6J * DBA)
|
abnormal germ cell morphology
|
J:179895
|
azoospermia
|
J:179895
|
Prdm9repro7/Prdm9repro7
(B6;C3Fe-Prdm9repro7/J)
|
arrest of male meiosis
|
J:92463
|
azoospermia
|
J:92463
|
Prdm9tm1.1Kpgn/Prdm9tm1.1Kpgn
(B6.Cg-Prdm9tm1.1Kpgn)
|
abnormal meiosis
|
J:222816
|
Prdm9tm1Ymat/Prdm9tm1Ymat
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal chromosomal synapsis
|
J:102875
|
abnormal double-strand DNA break repair
|
J:102875
|
abnormal female meiosis
|
J:102875
|
arrest of male meiosis
|
J:102875
|
azoospermia
|
J:102875
|
decreased oocyte number
|
J:102875
|
Prdm9tm1Ymat/Prdm9tm1Ymat
(C3.129P2(B6)-Prdm9tm1Ymat/HandJ)
|
abnormal female meiosis
|
J:299008
|
arrest of male meiosis
|
J:299008
|
decreased oocyte number
|
J:299008
|
Prdm9tm1Ymat/Prdm9tm1Ymat
(B6.129P2-Prdm9tm1Ymat)
|
abnormal chiasmata formation
|
J:299008
|
abnormal chromosomal synapsis
|
J:296124
|
abnormal double-strand DNA break repair
|
J:296124
|
abnormal female meiosis
|
J:299008
|
abnormal female meiosis I arrest
|
J:299008
|
Prdm9tm1Ymat/Prdm9tm1Ymat
(B6.Cg-Prdm9tm1Ymat)
|
cellular phenotype
|
J:280261
|
Prdm9tm1Ymat/Prdm9tm1Ymat Rad21ltm1b(KOMP)Wtsi/Rad21ltm1b(KOMP)Wtsi
(B6.Cg-Prdm9tm1Ymat Rad21ltm1b(KOMP)Wtsi)
|
cellular phenotype
|
J:280261
|
Prdm9tm1Ymat/Prdm9tm1Ymat Rec8tm1b(KOMP)Wtsi/Rec8tm1b(KOMP)Wtsi
(B6.Cg-Prdm9tm1Ymat Rec8tm1b(KOMP)Wtsi)
|
abnormal double-strand DNA break repair
|
J:280261
|
Prdm9tm1Ymat/Prdm9tm1Ymat Stag3tm1e.1(KOMP)Wtsi/Stag3tm1e.1(KOMP)Wtsi
(B6.Cg-Prdm9tm1Ymat Stag3tm1e.1(KOMP)Wtsi)
|
abnormal double-strand DNA break repair
|
J:280261
|
abnormal male meiosis
|
J:280261
|
Prdm11tm1.1Ahl/Prdm11tm1.1Ahl
(B6.129(C)-Prdm11tm1.1Ahl)
|
abnormal cell physiology
|
J:221379
|
increased megakaryocyte progenitor cell proliferation
|
J:222765
|
Prdm12tm1Ejbd/Prdm12tm1Ejbd
(involves: C57BL/6J * C57BL/6N)
|
increased neuron apoptosis
|
J:283226
|
Prdm14tm1e(EUCOMM)Wtsi/Prdm14tm1e(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal primordial germ cell morphology
|
J:200019
|
Prdm14tm1Sait/Prdm14tm1Sait
(B6.129P2-Prdm14tm1Sait)
|
absent germ cells
|
J:138571
|
Prdm14tm1Sait/Prdm14tm1Sait Tg(Prdm1-Venus)1Sait/0
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal primordial germ cell morphology
|
J:138571
|
decreased primordial germ cell number
|
J:138571
|
Prdm16tm1.1Brsp/Prdm16tm1.1Brsp Myf5tm1(cre)Mrc/Myf5+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cellular respiration
|
J:213153
|
decreased fat cell mitochondrial DNA content
|
J:213153
|
decreased mitochondrial number
|
J:213153
|
Prdm16tm1.1Brsp/Prdm16tm1.1Brsp Tg(Adipoq-cre)1Evdr/0
(involves: 129/Sv * C57BL/6 * FVB/N)
|
decreased adipocyte glucose uptake
|
J:208683
|
Prdm16tm1.1Brsp/Prdm16tm1.1Brsp Tg(myl7.L-cre)1118Tmhn/0
(involves: 129 * C57BL/6J * MF1)
|
decreased fetal cardiomyocyte proliferation
|
J:326525
|
Prdx1Gt(OST422296)Lex/Prdx1Gt(OST422296)Lex
(B6.Cg-Prdx1Gt(OST422296)Lex)
|
abnormal redox activity
|
J:103909
|
Prdx1tm1Rave/Prdx1+
(involves: 129S6/SvEvTac * C57BL/6)
|
increased cellular sensitivity to hydrogen peroxide
|
J:84677
|
increased cellular sensitivity to oxidative stress
|
J:84677
|
Prdx1tm1Rave/Prdx1tm1Rave
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell cycle
|
J:84677
|
decreased cell proliferation
|
J:84677
|
increased cellular sensitivity to hydrogen peroxide
|
J:84677
|
increased cellular sensitivity to oxidative stress
|
J:84677
|
Prdx1tm1Yu/Prdx1tm1Yu
(Not Specified)
|
increased keratinocyte apoptosis
|
J:306075
|
Prdx2tm1Yu/Prdx2tm1Yu
(involves: 129S4/SvJae)
|
increased cellular sensitivity to hydrogen peroxide
|
J:84271
|
increased cellular sensitivity to oxidative stress
|
J:84271
|
Prdx3Gt(Betageo-puro)711Lex/Prdx3Gt(Betageo-puro)711Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:118595
|
Prdx3tm1Hjha/Prdx3tm1Hjha
(involves: 129S4/SvJae * C57BL/6)
|
abnormal mitochondrial physiology
|
J:228860
|
abnormal redox activity
|
J:228860
|
abnormal white fat cell differentation
|
J:228860
|
decreased fatty acid oxidation
|
J:228860
|
oxidative stress
|
J:228860
|
Prdx4tm1.1Jufu/Y
(involves: C57BL/6)
|
increased male germ cell apoptosis
|
J:149074
|
oligozoospermia
|
J:149074
|
oxidative stress
|
J:149074
|
Prdx5tm1.1(KOMP)Vlcg/Prdx5tm1.1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
abnormal cellular respiration
|
J:271141
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:271141
|
abnormal redox activity
|
J:271141
|
oxidative stress
|
J:271141
|
Prdx5tm1Dsle/Prdx5tm1Dsle
(involves: C57BL/6)
|
oxidative stress
|
J:294801
|
Prdx6tm1Pgn/Prdx6tm1Pgn
(either: 129/Sv or (involves: 129/Sv * C57BL/6))
|
oxidative stress
|
J:84376
|
Prex1tm1Dwu/Prex1tm1Dwu
(Not Specified)
|
impaired neutrophil chemotaxis
|
J:102213
|
Prex1tm1Hcew/Prex1tm1Hcew
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:102214
|
Prf1tm1Sdz/Prf1tm1Sdz
(C57BL/6-Prf1tm1Sdz/J)
|
decreased NK cell degranulation
|
J:193137
|
Prf1tm1Tsc/Prf1tm1Tsc
(129X1.129S2-Prf1tm1Tsc)
|
decreased T cell apoptosis
|
J:126114
|
Prickle1tm1Nue/Prickle1tm1Nue
(involves: C57BL/6 * CBA)
|
abnormal anterior visceral endoderm cell migration
|
J:151993
|
abnormal mitotic spindle morphology
|
J:151993
|
decreased mitotic index
|
J:151993
|
increased embryonic tissue cell apoptosis
|
J:151993
|
Prickle3em1Mxg/Y
(C57BL/6JSlacc-Prickle3em1Mxg)
|
abnormal mitochondrial morphology
|
J:300151
|
Prickle3em1Mxg/Prickle3+
(C57BL/6JSlacc-Prickle3em1Mxg)
|
abnormal mitochondrial morphology
|
J:300151
|
Primpoltm1.2Ado/Primpoltm1.2Ado
(involves: 129 * C57BL/6J)
|
abnormal mitosis
|
J:206155
|
Prkaa1tm1.1Sjm/Prkaa1tm1.1Sjm Prkaa2tm1.1Sjm/Prkaa2tm1.1Sjm Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA * SJL)
|
cellular phenotype
|
J:165090
|
increased mitochondrial fission
|
J:165090
|
Prkaa1tm1Sbj/Prkaa1tm1Sbj
(involves: 129S2/SvPas * C57BL/6J)
|
decreased skeletal muscle cell glucose uptake
|
J:87719
|
Prkaa1tm1Sbj/Prkaa1tm1Sbj
(involves: 129S2/SvPas)
|
impaired granulosa cell differentiation
|
J:324163
|
Prkaa1tm1Sbj/Prkaa1tm1Sbj Prkaa2tm1.1Vio/Prkaa2tm1.1Vio
(involves: 129S2/SvPas)
|
cellular phenotype
|
J:141132
|
Prkaa2tm1.1Vio/Prkaa2tm1.1Vio
(involves: 129S2/SvPas)
|
decreased skeletal muscle cell glucose uptake
|
J:87719
|
increased skeletal muscle cell glucose uptake
|
J:87719
|
Prkab1Gt(RRR454)Byg/Prkab1Gt(RRR454)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuron differentiation
|
J:146618
|
abnormal neuronal precursor proliferation
|
J:146618
|
Prkab1tm1Grst/Prkab1tm1Grst Prkab2tm1Grst/Prkab2tm1Grst Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6 * FVB)
|
decreased muscle cell glucose uptake
|
J:176578
|
Prkab2Gt(AL0483)Wtsi/Prkab2Gt(AL0483)Wtsi
(B6.129P2-Prkab2Gt(AL0483)Wtsi)
|
decreased muscle cell glucose uptake
|
J:186658
|
Prkab2tm1.1Grst/Prkab2tm1.1Grst
(involves: C57BL/6)
|
decreased skeletal muscle cell glucose uptake
|
J:167339
|
increased muscle cell glucose uptake
|
J:167339
|
Prkacatm1Gsm/Prkaca+ Prkacbtm1Gsm/Prkacbtm1Gsm
(involves: 129X1/SvJ * C57BL/6)
|
increased neural tube apoptosis
|
J:76765
|
Prkacatm1Gsm/Prkacatm1Gsm
(involves: 129X1/SvJ * C57BL/6)
|
asthenozoospermia
|
J:77110
|
Prkacatm2Gsm/Prkacatm2Gsm
(involves: 129X1/SvJ * C57BL/6)
|
asthenozoospermia
|
J:92616
|
Prkacatm4.1Gsm/Prkacatm4.1Gsm
(involves: C57BL/6)
|
abnormal sperm motility
|
J:163375
|
Prkar1atm1.2Lsk/Prkar1a+ Rb1tm2Brn/Rb1+ Tg(Col1a1-cre)1Kry/0 Trp53tm1Brn/Trp53tm1Brn
(involves: 129 * 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * FVB/N)
|
increased cell migration
|
J:234128
|
Prkar1atm1Gsm/Prkar1atm1Gsm
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell morphology
|
J:78010
|
Prkar1atm1Lsk/Prkar1atm1Lsk Tg(Akr1b7-cre)1Anm/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased adrenal gland apoptosis
|
J:161521
|
retention of the adrenal gland x-zone
|
J:161521
|
Prkcatm1Far/Prkcatm1Far
(involves: 129/Sv * 129P2/OlaHsd)
|
increased adipocyte glucose uptake
|
J:85923
|
increased skeletal muscle cell glucose uptake
|
J:85923
|
Prkcbtilc/Prkcbtilc
(involves: C57BL/6JSfdAnu)
|
decreased B cell proliferation
|
J:221236
|
Prkcbtm1Tara/Prkcbtm1Tara
(involves: 129)
|
decreased B cell proliferation
|
J:34818
|
Prkcdtm1Kin/Prkcdtm1Kin
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:76135,
J:143854
|
Prkcdtm1Kin/Prkcdtm1Kin
(involves: 129P2/OlaHsd)
|
abnormal osteoblast differentiation
|
J:117333
|
Prkcdtm1Qxu/Prkcdtm1Qxu
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell apoptosis
|
J:76134
|
Prkcdtm1Qxu/Prkcdtm1Qxu Tg(IghelMD4)4Ccg/0 Tg(ML5sHEL)5Ccg/0
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal B cell proliferation
|
J:76134
|
Prkcetm1Bsca/Prkcetm1Bsca
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased macrophage apoptosis
|
J:103337
|
decreased T cell proliferation
|
J:103337
|
Prkchtm1.2Gasc/Prkchtm1.2Gasc
(involves: C57BL/6 * FVB/N * SJL)
|
decreased T cell proliferation
|
J:186080
|
Prkchtm1.2Gasc/Prkchtm1.2Gasc Prkcqtm1Litt/Prkcqtm1Litt
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL)
|
decreased T cell proliferation
|
J:186080
|
Prkcitm1.1Rfar/Prkcitm1.1Rfar
(involves: 129P2/OlaHsd * BALB/cJ * NMRI)
|
abnormal cell morphology
|
J:202124
|
Prkcitm1Hed/Prkcitm1Hed
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell morphology
|
J:92719
|
Prkcitm1Kido/Prkcitm1.1Kido Tg(Nphs1-cre)33Mska/0
(involves: C57BL/6 * C57BL/6N * DBA/2)
|
detached podocyte
|
J:144995
|
Prkcitm1Rfar/Prkci+ Tg(Ckmm-cre)5Khn/?
(involves: 129P2/OlaHsd * C57BL/6 * FVB)
|
decreased adipocyte glucose uptake
|
J:123964
|
decreased cardiac muscle cell glucose uptake
|
J:123964
|
decreased muscle cell glucose uptake
|
J:123964
|
decreased skeletal muscle cell glucose uptake
|
J:123964
|
Prkcitm1Rfar/Prkcitm1Rfar Tg(Ckmm-cre)5Khn/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB)
|
decreased adipocyte glucose uptake
|
J:123964
|
decreased cardiac muscle cell glucose uptake
|
J:123964
|
decreased skeletal muscle cell glucose uptake
|
J:123964
|
Prkcqtm1.1Bai/Prkcqtm1.1Bai
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased T cell proliferation
|
J:83733
|
Prkcqtm1Litt/Prkcqtm1Litt
(involves: 129P2/OlaHsd)
|
decreased T cell proliferation
|
J:83922,
J:123989
|
Prkcqtm1Litt/Prkcqtm1Litt
(B6.129P2-Prkcqtm1Litt)
|
decreased splenocyte proliferation
|
J:129421
|
decreased T cell proliferation
|
J:94285
|
Prkcqtm1Litt/Prkcqtm1Litt
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal adipocyte glucose uptake
|
J:92834
|
abnormal muscle cell glucose uptake
|
J:92834
|
decreased T cell proliferation
|
J:186080
|
increased T cell apoptosis
|
J:141128
|
Prkcqtm1Litt/Prkcqtm1Litt
(either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6))
|
decreased T cell apoptosis
|
J:141930
|
decreased T cell proliferation
|
J:141930
|
Prkcqtm1Litt/Prkcqtm1Litt Tcratm1Mom/Tcratm1Mom
(involves: 129P2/OlaHsd * 129S2/SvPas)
|
decreased T cell proliferation
|
J:135589
|
Prkcqtm1Litt/Prkcqtm1Litt Tg(DO11.10)10Dlo/0
(involves: 129 * BALB/c * C3H * C57BL/6)
|
decreased T cell apoptosis
|
J:141930
|
Prkcqtm1Litt/Prkcqtm1Litt Tg(TcrLCMV)327Sdz/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
decreased splenocyte proliferation
|
J:123989
|
decreased T cell proliferation
|
J:123989
|
Prkdcdxnph/Prkdcdxnph
(BALB/c)
|
increased cellular sensitivity to gamma-irradiation
|
J:68487
|
Prkdcscid/Prkdcscid
(C.BKa-Prkdcscid)
|
decreased B cell proliferation
|
J:6958
|
decreased T cell proliferation
|
J:6958
|
Prkdcscid/Prkdcscid
(NOD.Cg-Prkdcscid)
|
increased cellular sensitivity to X-ray irradiation
|
J:109833
|
Prkdcscid/Prkdcscid Tgfb1tm1Doe/Tgfb1tm1Doe
(involves: 129 * C3H * CF-1)
|
decreased elongated spermatid number
|
J:129629
|
oligozoospermia
|
J:129629
|
PrkdcTg(INS-PDE2)5-1Lmb/?
(involves: FVB/N)
|
increased cellular sensitivity to gamma-irradiation
|
J:108405
|
Prkdctm1.1Bpcc/Prkdctm1.1Bpcc
(involves: 129 * C57BL/6)
|
abnormal DNA repair
|
J:171351
|
increased cellular sensitivity to alkylating agents
|
J:171351
|
increased cellular sensitivity to ionizing radiation
|
J:171351
|
increased cellular sensitivity to ultraviolet irradiation
|
J:171351
|
increased sensitivity to induced cell death
|
J:171351
|
increased small intestinal crypt cell apoptosis
|
J:171351
|
Prkdctm1Fwa/Prkdctm1Fwa
(involves: 129S6/SvEvTac * C57BL/6)
|
increased cellular sensitivity to ionizing radiation
|
J:50221
|
Prkdctm1Gcl/Prkdctm1Gcl
(involves: 129S1/Sv * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:53765
|
Prkdctm1Gcl/Prkdctm1Gcl
(involves: 129S1/Sv)
|
cellular phenotype
|
J:126920
|
decreased thymocyte apoptosis
|
J:126920
|
Prkdctm1Get/Prkdc+ Rad54ltm1Jhjh/Rad54ltm1Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal chromosome morphology
|
J:84801
|
decreased telomere length
|
J:84801
|
Prkdctm1Get/Prkdctm1Get
(involves: 129S4/SvJae * Black Swiss)
|
increased cellular sensitivity to gamma-irradiation
|
J:50222
|
Prkdctm1Get/Prkdctm1Get Rad54ltm1Jhjh/Rad54ltm1Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal chromosome morphology
|
J:84801
|
Prkg1tm1Hfm/Prkg1tm1Hfm
(involves: C57BL/6N)
|
decreased fat cell mitochondrial DNA content
|
J:199222
|
Prkntm1Ccs/Prkntm1Ccs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:168847
|
Prkntm1Ccs/Prkntm1Ccs Tg(CAG-SNCA*)1.1Ccs/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cellular respiration
|
J:127707
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:127707
|
abnormal mitochondrial morphology
|
J:127707
|
Prkntm1Ccs/Prkntm1Ccs Tg(Th-SNCA*)1.2Ccs/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cellular respiration
|
J:127707
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:127707
|
abnormal mitochondrial morphology
|
J:127707
|
Prkntm1Roo/Prkntm1Roo
(involves: 129S2/SvPas)
|
increased neuron apoptosis
|
J:125148
|
Prkntm1Shn/Prkntm1Shn
(B6.129S4-Prkntm1Shn/J)
|
abnormal autophagy
|
J:193741
|
abnormal mitochondrial morphology
|
J:193741
|
abnormal mitochondrial physiology
|
J:193741
|
abnormal mitophagy
|
J:193741
|
decreased mitochondrial size
|
J:193741
|
increased sensitivity to induced cell death
|
J:193741,
J:194987
|
Prkntm1Shn/Prkntm1Shn Slc6a3tm4.1(tTA)Xz/? Tg(tetO-SNCA*A53T)E2Cai/?
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6)
|
abnormal mitochondrial morphology
|
J:218892
|
Prkntm1Ykt/Prkntm1Ykt Tg(Prp-GPR37)1Ryot/0
(involves: 129P2/OlaHsd * C3H * C57BL/6)
|
abnormal redox activity
|
J:140326
|
oxidative stress
|
J:140326
|
Prkntm1Ykt/Prkntm1Ykt Tg(Prp-GPR37)1Ryot/Tg(Prp-GPR37)1Ryot
(involves: 129P2/OlaHsd * C3H * C57BL/6)
|
abnormal redox activity
|
J:140326
|
Prl7b1tm1(KOMP)Vlcg/Prl7b1tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
maternal effect
|
J:236336
|
Prl7d1em1Liga/Prl7d1em1Liga
(involves: C57BL/6)
|
maternal effect
|
J:288761
|
Prlrtm1Cnp/Prlr+
(B6.129P2-Prlrtm1Cnp/J)
|
abnormal neuron proliferation
|
J:83248
|
Prlrtm1Cnp/Prlrtm1Cnp
(either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6))
|
abnormal oogenesis
|
J:38093
|
Prm1tm1Eddy/Prm1+
(either: (chimera involves: 129P2/OlaHsd * C57BL/6N) or (chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6N))
|
immotile sperm
|
J:69127
|
teratozoospermia
|
J:69127
|
Prm2em1Hsc/Prm2em1Hsc
(involves: C57BL/6 * DBA/2)
|
abnormal sperm head morphology
|
J:295027,
J:243626
|
abnormal sperm midpiece morphology
|
J:243626
|
abnormal sperm nucleus morphology
|
J:295027,
J:243626
|
abnormal spermatid morphology
|
J:243626
|
detached acrosome
|
J:243626
|
immotile sperm
|
J:243626
|
necrospermia
|
J:295027
|
oxidative stress
|
J:295027
|
small sperm head
|
J:295027
|
Prm2em2Hsc/Prm2em2Hsc
(involves: C57BL/6 * DBA/2)
|
abnormal sperm head morphology
|
J:295027,
J:243626
|
abnormal sperm midpiece morphology
|
J:243626
|
abnormal sperm nucleus morphology
|
J:295027,
J:243626
|
abnormal spermatid morphology
|
J:243626
|
detached acrosome
|
J:243626
|
immotile sperm
|
J:243626
|
necrospermia
|
J:295027
|
oxidative stress
|
J:295027
|
small sperm head
|
J:295027
|
Prm2tm1Eddy/Prm2+
(either: (chimera involves: 129P2/OlaHsd * C57BL/6N) or (chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6N))
|
immotile sperm
|
J:69127
|
teratozoospermia
|
J:89324,
J:69127
|
Prm3tm1Grz/Prm3tm1Grz
(involves: 129/Sv * C57BL/6)
|
abnormal sperm motility
|
J:140818
|
Prmt1tm1Hkim/Prmt1tm1Hkim Tg(Neurog3-cre)24Syos/0
(Not Specified)
|
arrest of male meiosis
|
J:324166
|
azoospermia
|
J:324166
|
increased male germ cell apoptosis
|
J:324166
|
Prmt2tm1Enbl/Prmt2tm1Enbl
(involves: 129S2/SvPas)
|
abnormal cell cycle
|
J:111352
|
Prmt5Gt(RRA014)Byg/Prmt5Gt(RRA014)Byg
(involves: 129P2/OlaHsd)
|
absent inner cell mass proliferation
|
J:166736
|
Prmt5tm2c(EUCOMM)Wtsi/Prmt5tm2c(EUCOMM)Wtsi Tg(Nes-cre)1Kln/0
(B6.Cg-Prmt5tm2c(EUCOMM)Wtsi Tg(Nes-cre)1Kln)
|
abnormal neuronal precursor proliferation
|
J:201152
|
increased neuron apoptosis
|
J:201152
|
Prmt6tm1.2Rchd/Prmt6tm1.2Rchd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal cell cycle
|
J:199753
|
decreased fibroblast proliferation
|
J:199753
|
early cellular replicative senescence
|
J:199753
|
Prmt6tm1.2Rchd/Prmt6tm1.2Rchd Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * FVB/N)
|
cellular phenotype
|
J:199753
|
Prmt7tm1.1Rchd/Prmt7tm1.1Rchd Pax7tm1(cre/ERT2)Gaka/Pax7+
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6NCrl)
|
early cellular replicative senescence
|
J:271361
|
Prmt7tm1.2Rchd/Prmt7tm1.2Rchd
(involves: 129S4/SvJaeSor * FVB/N)
|
abnormal myoblast differentiation
|
J:271361
|
early cellular replicative senescence
|
J:271361
|
Prndtm1Aag/Prndtm1Aag
(involves: 129P2/OlaHsd)
|
abnormal acrosome morphology
|
J:91621
|
abnormal sperm head morphology
|
J:91621
|
asthenozoospermia
|
J:91621
|
hairpin sperm flagellum
|
J:91621
|
oligozoospermia
|
J:91621
|
teratozoospermia
|
J:91621
|
Prnp/Prndtm1Aag/Prnp/Prndtm1Aag
(Not Specified)
|
teratozoospermia
|
J:89232
|
Prnp/Prndtm1Aag/Prnp/Prndtm1Aag
(Not Specified)
|
teratozoospermia
|
J:89232
|
Prnptm2Edin/Prnptm2Edin
(B6.129P2-Prnptm2Edin)
|
abnormal neuron differentiation
|
J:107170
|
abnormal neuronal precursor proliferation
|
J:107170
|
Prnptm2Edin/Prnptm2Edin Tg(Prnp)a20Cwe/0
(B6.Cg-Prnptm2Edin Tg(Prnp)a20Cwe)
|
abnormal neuronal precursor proliferation
|
J:107170
|
premature neuronal precursor differentiation
|
J:107170
|
Prnptm2Lnq/Prnptm2Lnq
(involves: 129P2/OlaHsd * C57BL/6N)
|
abnormal neuron proliferation
|
J:200974
|
increased neuron apoptosis
|
J:200974
|
Prnptm3Lnq/Prnptm3Lnq
(involves: 129P2/OlaHsd * C57BL/6N)
|
abnormal neuron proliferation
|
J:200974
|
increased neuron apoptosis
|
J:200974
|
Prokr2tm1Api/Prokr2tm1Api
(involves: C57BL/6 * CBA)
|
abnormal axon extension
|
J:107587
|
arrest of male meiosis
|
J:107587
|
azoospermia
|
J:107587
|
Prom1tm1.1(DTA)Toko/Prom1tm1.1(DTA)Toko Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * CBA * SJL)
|
increased brain apoptosis
|
J:152390
|
Prorptm1.1Afi/Prorptm1.1Afi Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6N * FVB)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:238964
|
abnormal mitochondrial physiology
|
J:238964
|
Prox1tm1Gco/Prox1tm1Gco
(involves: 129S1/Sv * 129X1/SvJ * NMRI)
|
decreased hepatocyte proliferation
|
J:63128
|
Prpf19tm1Glri/Prpf19tm1Glri
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:121379
|
absent inner cell mass proliferation
|
J:121379
|
decreased cell proliferation
|
J:121379
|
Prph2Nmf193/Prph2+
(C57BL/6J-Prph2Nmf193)
|
increased retina apoptosis
|
J:148636
|
Prph2tm1Nmc/Prph2tm1Nmc
(involves: 129S1/Sv * 129X1/SvJ)
|
increased retina apoptosis
|
J:76490
|
Prps2tm1a(KOMP)Wtsi/Y Tg(IghMyc)22Bri/0
(involves: C57BL/6N * SJL)
|
increased B cell apoptosis
|
J:214383
|
Prr19em1Atot/Prr19em1Atot
(either: (involves: C57BL/6JCrl) or (involves: CD-1))
|
abnormal double-strand DNA break repair
|
J:292293
|
abnormal meiosis
|
J:292293
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:292293
|
decreased oocyte number
|
J:292293
|
increased male germ cell apoptosis
|
J:292293
|
oligozoospermia
|
J:292293
|
teratozoospermia
|
J:292293
|
Prr19em2Atot/Prr19em2Atot
(either: (involves: C57BL/6JCrl) or (involves: CD-1))
|
abnormal double-strand DNA break repair
|
J:292293
|
abnormal meiosis
|
J:292293
|
Prrc2atm1Fcw/Prrc2atm1Fcw Olig2tm2(TVA,cre)Rth/Olig2+
(involves: 129 * C57BL/6)
|
decreased oligodendrocyte progenitor number
|
J:301796
|
Prrc2atm1Fcw/Prrc2atm1Fcw Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
decreased oligodendrocyte progenitor number
|
J:301796
|
Prss8em1Bug/Prss8em1Bug Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * NIH Black Swiss)
|
abnormal enterocyte proliferation
|
J:261068
|
abnormal intestinal goblet cell morphology
|
J:261068
|
decreased colon goblet cell number
|
J:261068
|
Prss21tm1Anta/Prss21tm1Anta
(involves: NIH Black Swiss)
|
abnormal sperm flagellum morphology
|
J:154521
|
abnormal sperm head morphology
|
J:154521
|
coiled sperm flagellum
|
J:154521
|
decreased sperm progressive motility
|
J:154521
|
detached sperm flagellum
|
J:154521
|
hairpin sperm flagellum
|
J:154521
|
oligozoospermia
|
J:154521
|
teratozoospermia
|
J:154521
|
Prss34tm1.1Hkar/Prss34tm1.1Hkar
(involves: C57BL/6)
|
cellular phenotype
|
J:238924
|
Prss37tm1Zgwg/Prss37tm1Zgwg
(involves: 129S6/SvEvTac * C57BL/6J)
|
impaired sperm migration in female genital tract
|
J:202066
|
Prss50em1Cajj/Prss50em1Cajj
(involves: C57BL/6J)
|
abnormal sperm annulus morphology
|
J:305434
|
abnormal sperm axoneme morphology
|
J:305434
|
abnormal spermatid morphology
|
J:305434
|
absent sperm flagellum
|
J:305434
|
absent sperm mitochondrial sheath
|
J:305434
|
asthenozoospermia
|
J:305434
|
decreased hyperactivated sperm motility
|
J:305434
|
decreased sperm progressive motility
|
J:305434
|
immotile sperm
|
J:305434
|
multi-headed sperm
|
J:305434
|
multiflagellated sperm
|
J:305434
|
teratozoospermia
|
J:305434
|
Prss54tm1Zgwg/Prss54tm1Zgwg
(involves: C57BL/6J * C57BL/6N)
|
abnormal acrosome morphology
|
J:332475
|
Prss55em1Huizh/Prss55em1Huizh
(Not Specified)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:307639
|
abnormal mitochondrial crista morphology
|
J:307639
|
abnormal outer dense fiber morphology
|
J:307639
|
abnormal sperm axoneme morphology
|
J:307639
|
abnormal sperm flagellum morphology
|
J:307639
|
abnormal sperm head morphology
|
J:307639
|
abnormal sperm mitochondrial sheath morphology
|
J:307639
|
asthenozoospermia
|
J:307639
|
coiled sperm flagellum
|
J:307639
|
decreased sperm progressive motility
|
J:307639
|
teratozoospermia
|
J:307639
|
Prss55tm1Zgwg/Prss55tm1Zgwg
(involves: 129 * C57BL/6)
|
impaired sperm migration in female genital tract
|
J:278420
|
Prss59em1Fcw/Prss59em1Fcw
(involves: C57BL/6)
|
impaired sperm migration in female genital tract
|
J:303285
|
Prtgtm1.1Mjfn/Prtgtm1.1Mjfn
(B6.129-Prtgtm1.1Mjfn)
|
increased cranial neural crest cell apoptosis
|
J:311848
|
Prtn3tm1.1Hrlu/Prtn3tm1.1Hrlu
(involves: C57BL/6)
|
decreased apoptosis
|
J:217636
|
Prxl2atm1(KOMP)Vlcg/Prxl2atm1(KOMP)Vlcg
(C57BL/6N-Prxl2atm1(KOMP)Vlcg)
|
increased endoplasmic reticulum stress
|
J:234040
|
Ps/Ps
(involves: 101/H * C3H/HeH * C57BL/Gr * CBA/Gr)
|
abnormal interdigital cell death
|
J:5125
|
absent interdigital cell death
|
J:5125
|
Psaptm1Suz/Psaptm1Suz
(involves: 129P2/OlaHsd)
|
decreased male germ cell number
|
J:106511
|
Psaptm2Suz/Psaptm2Suz
(involves: 129S/SvEv * C57BL/6J)
|
enhanced autophagy
|
J:198242
|
Psaptm4.1Ggb/Psaptm4.1Ggb
(involves: 129S/SvEv * C57BL/6J)
|
enhanced autophagy
|
J:198242
|
Psen1tm1Bdes/Psen1tm1Bdes
(involves: 129P2/OlaHsd)
|
enhanced neuronal migration
|
J:95663
|
Psen1tm1Jzt/Psen1tm1Jzt Psen2tm1Ber/Psen2tm1Ber Tg(Camk2a-cre)T29-1Stl/0
(involves: C57BL/6 * CBA)
|
abnormal apoptosis
|
J:90685
|
Psen1tm1Jzt/Psen1tm1Jzt Tg(Camk2a-cre)T29-1Stl/0
(involves: C57BL/6 * CBA)
|
decreased cell proliferation
|
J:73252
|
Psen1tm1Mpm/Psen1tm1Mpm
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased susceptibility to neuronal excitotoxicity
|
J:51950
|
Psen1tm1Mpm/Psen1tm1Pcw
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6)
|
abnormal neuron differentiation
|
J:91277
|
Psen1tm1Shn/Psen1tm1Shn
(Not Specified)
|
abnormal apoptosis
|
J:90392
|
Psen1tm1Shn/Psen1tm1Shn
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal neuron differentiation
|
J:40365
|
Psen1tm1Shs/Psen1tm1Shs
(involves: C57BL/6)
|
abnormal neuron differentiation
|
J:91975
|
abnormal neuronal precursor proliferation
|
J:91975
|
enhanced neuronal migration
|
J:91975
|
premature neuronal precursor differentiation
|
J:91975
|
Psen2tm1Bdes/Psen2tm1Bdes
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased lung apoptosis
|
J:58118
|
increased lung endothelial cell apoptosis
|
J:58118
|
Psip1tm1Eng/Psip1tm1Eng Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal cell physiology
|
J:177408
|
Psma8em1Yuc/Psma8em1Yuc
(C57BL/6-Psma8em1Yuc)
|
abnormal spermatocyte morphology
|
J:279342
|
arrest of male meiosis
|
J:279342
|
azoospermia
|
J:279342
|
decreased spermatid number
|
J:279342
|
Psmb10tm1Mgro/Psmb10tm1Mgro
(involves: 129S2/SvPas * C57BL/6)
|
decreased T cell proliferation
|
J:125058
|
Psmb11tm1(Psmb8)Khog/Psmb11tm1(Psmb8)Khog
(involves: C57BL/6)
|
increased T cell proliferation
|
J:196156
|
Psmc1tm1Maye/Psmc1tm1Maye Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-cre)1Lin/0
(involves: 129 * C57BL/6 * CD-1)
|
increased neuron apoptosis
|
J:138991
|
Psmc3iptm1Rdco/Psmc3iptm1Rdco
(involves: 129S6/SvEvTac)
|
abnormal male meiosis
|
J:207221,
J:194067
|
abnormal meiosis
|
J:109004
|
absent gametes
|
J:109004
|
arrest of male meiosis
|
J:109004
|
azoospermia
|
J:109004
|
Psmc3iptm1Rdco/Psmc3iptm1Rdco Spo11tm1.1Gvpc/Spo11tm1.1Gvpc
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:202231
|
Psmd4tm1Smta/Psmd4tm1Smta
(involves: C57BL/6 * CBA)
|
absent inner cell mass proliferation
|
J:126546
|
Psmd11tm1.1Qit/Psmd11tm1.1Qit Gt(ROSA)26Sortm3(CAG-Cre/ERT2)Dsa/Gt(ROSA)26Sor+ Tg(ACTFLPe)9205Dym/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased apoptosis
|
J:301736
|
Psme3tm1Jjm/Psme3tm1Jjm
(B6.129X1-Psme3tm1Jjm)
|
abnormal cell cycle checkpoint function
|
J:88626
|
decreased fibroblast proliferation
|
J:88626
|
Psme3tm1Tchi/Psme3tm1Tchi
(involves: C57BL/6J * CBA)
|
decreased cell proliferation
|
J:89182
|
Psme4tm1Slek/Psme4tm1Slek
(involves: 129 * C57BL/6)
|
abnormal male germ cell morphology
|
J:107376
|
abnormal spermatid morphology
|
J:107376
|
abnormal spermatocyte morphology
|
J:107376
|
asthenozoospermia
|
J:107376
|
multinucleated giant male germ cells
|
J:107376
|
teratozoospermia
|
J:107376
|
Psme4tm1Tchi/Psme4tm1Tchi
(involves: C57BL/6)
|
abnormal spermatid morphology
|
J:197675
|
increased male germ cell apoptosis
|
J:197675
|
Psmg1tm1.1Smta/Psmg1tm1.1Smta Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * CBA * SJL)
|
decreased cerebellar granule cell precursor proliferation
|
J:162790
|
Pstpip2Lupo/Pstpip2Lupo
(either: (involves: C3HeB/FeJ) or (involves: C3HeB/FeJ * C57BL/6J))
|
cellular necrosis
|
J:125785
|
Pstpip2m1Bcs/Pstpip2m1Bcs
(involves: C57BL/6)
|
cellular necrosis
|
J:196534
|
Ptbp1tm1Msol/Ptbp1tm1Msol
(B6J.129-Ptbp1tm1Msol)
|
decreased cell proliferation
|
J:223915
|
increased apoptosis
|
J:223915
|
Ptbp1tm1Nobu/Ptbp1tm2Nobu Emx1tm1(cre)Ito/Emx1+
(involves: 129P2/OlaHsd)
|
abnormal brain ependyma motile cilium morphology
|
J:213479
|
Ptbp1tm1Nobu/Ptbp1tm2Nobu Tg(Nes-cre)1Sasa/0
(involves: 129P2/OlaHsd)
|
premature neuronal precursor differentiation
|
J:213479
|
Ptbp2Gt(NPX210)Byg/Ptbp2Gt(NPX210)Byg
(involves: 129P2/OlaHsd)
|
abnormal neuron differentiation
|
J:185949
|
premature neuronal precursor differentiation
|
J:185949
|
Ptbp2tm1.1Rbd/Ptbp2tm1.1Rbd
(Not Specified)
|
abnormal neuron differentiation
|
J:185949
|
premature neuronal precursor differentiation
|
J:185949
|
Ptcd1tm1(KOMP)Vlcg/Ptcd1+
(C57BL/6N-Ptcd1tm1(KOMP)Vlcg)
|
abnormal hepatocyte mitochondrial morphology
|
J:256004
|
abnormal mitochondrial crista morphology
|
J:256004
|
abnormal mitochondrial physiology
|
J:256004
|
abnormal oxidative phosphorylation
|
J:256004
|
Ptcd2Gt(RRF537)Byg/Ptcd2Gt(RRF537)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:143946
|
abnormal mitochondrial morphology
|
J:143946
|
Ptch1tm1Bjw/Ptch1tm1Bjw Tg(Atoh1-cre)1Bfri/0
(involves: 129T2/SvEms * C57BL/6 * CBA)
|
abnormal neuronal precursor proliferation
|
J:139573
|
Ptch1tm1Bjw/Ptch1tm1Bjw Tg(Atoh1-cre/Esr1*)14Fsh/0
(involves: 129T2/SvEms * FVB/N)
|
abnormal neuronal precursor proliferation
|
J:139573
|
Ptch1tm1Yy/Ptch1tm1.1Yy Tg(Col2a1-cre)1Bhr/0
(involves: C57BL/6 * SJL)
|
abnormal osteoblast differentiation
|
J:112462
|
increased chondrocyte proliferation
|
J:112462
|
Ptch1tm1Zim/Ptch1tm1Zim Stiltm1Mku/Stiltm1Mku
(involves: 129 * C57BL/6 * CD-1)
|
abnormal apoptosis
|
J:72500
|
Ptch1wig/Ptch1wig
(involves: 129S1/Sv * C57BL/6 * FVB/NJ)
|
abnormal neuron differentiation
|
J:171522
|
Ptentm1.1Yxy/Ptentm1.1Yxy
(involves: C57BL/6)
|
abnormal cellular respiration
|
J:308567
|
abnormal endocytosis
|
J:290673
|
abnormal mitochondrial morphology
|
J:308567
|
abnormal mitophagy
|
J:308567
|
cellular phenotype
|
J:290673,
J:308567
|
disorganized mitochondrial cristae
|
J:308567
|
increased myocardial fiber mitochondrial DNA content
|
J:308567
|
Ptentm1Engc/Pten+
(involves: CD-1)
|
abnormal cell physiology
|
J:197051
|
Ptentm1Engc/Ptentm1Engc
(involves: CD-1)
|
increased cell proliferation
|
J:210487
|
Ptentm1Hwu/Ptentm1Hwu Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
abnormal macrophage chemotaxis
|
J:148947
|
Ptentm1Hwu/Ptentm1Hwu Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S4/SvJae * C57BL/6 * DBA)
|
increased hepatocyte apoptosis
|
J:218587
|
increased hepatocyte proliferation
|
J:218587
|
oxidative stress
|
J:218587
|
Ptentm1Hwu/Ptentm1Hwu Tg(CYP19A1-cre)1Jri/0
(involves: 129S4/SvJae)
|
decreased granulosa cell apoptosis
|
J:138315
|
impaired luteal cell differentiation
|
J:138315
|
increased granulosa cell proliferation
|
J:138315
|
Ptentm1Hwu/Ptentm1Hwu Tg(Gdf9-icre)5092Coo/0
(B6.Cg-Ptentm1Hwu Tg(Gdf9-icre)5092Coo)
|
abnormal oocyte morphology
|
J:131827
|
Ptentm1Hwu/Ptentm1Hwu Tg(GFAP-cre)25Mes/0
(involves: 129S4/SvJae * FVB/N)
|
abnormal Bergmann glial cell differentiation
|
J:100428
|
Ptentm1Hwu/Ptentm1Hwu Tg(Gfap-cre)77.6Mvs/0
(involves: 129S4/SvJae * BALB/c * C57BL/6NHsd)
|
abnormal neuron differentiation
|
J:146630
|
abnormal neuronal precursor proliferation
|
J:146630
|
Ptentm1Hwu/Ptentm1Hwu Tg(Ins2-cre)25Mgn/0
(involves: 129S4/SvJae * C57BL/6 * DBA)
|
decreased cellular sensitivity to oxidative stress
|
J:106937
|
increased pancreatic beta cell proliferation
|
J:106937
|
Ptentm1Hwu/Ptentm1Hwu Tg(Nkx2-1-cre)2Sand/0
(involves: 129S4/SvJae * BALB/c * C57BL/6)
|
increased lung endothelial cell proliferation
|
J:167962
|
Ptentm1Hwu/Ptentm1Hwu Tg(Vil1-cre)997Gum/0
(involves: 129S4/SvJae * BALB/c * C57BL/6J * SJL)
|
abnormal intestinal goblet cell morphology
|
J:150553
|
abnormal small intestinal crypt cell proliferation
|
J:150553
|
Ptentm1Hwu/Ptentm1Hwu Vhltm1Jae/Vhltm1Jae Tg(Cdh16-cre)91Igr/0
(involves: 129S4/SvJae * BALB/c * C57BL/6J * ICR)
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:137073
|
increased kidney cell proliferation
|
J:137073
|
Ptentm1Mro/Ptentm1Mro Tg(En2-cre)22Alj/0
(Not Specified)
|
impaired neuronal migration
|
J:77123
|
Ptentm1Ppp/Pten+ Rac1tm1Tyb/Rac1tm2Tyb Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S/Sv * C3H * C57BL/6 * CBA)
|
abnormal apoptosis
|
J:173526
|
Ptentm1Rdp/Ptentm1Rdp Terttm1Rdp/Terttm1Rdp Trp53tm1Brn/Trp53tm1Brn Tg(Pbsn-cre)4Prb/0
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2)
|
decreased telomere length
|
J:186105
|
Ptentm1Rdp/Ptentm1Rdp Terttm3Rdp/Terttm3Rdp Trp53tm1Brn/Trp53tm1Brn Tg(Pbsn-cre)4Prb/0
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * DBA/2)
|
abnormal chromosome morphology
|
J:186105
|
increased telomere length
|
J:186105
|
Ptentm2.1Ppp/Ptentm2.1Ppp Tg(GFAP-TAg121)1Tvd/0
(involves: 129S1/Sv * C57BL/6 * C57BL/6J * DBA/2 * FVB/N)
|
abnormal astrocyte apoptosis
|
J:99385
|
Ptentm2Mak/Ptentm2Mak Smad4tm2.1Cxd/Smad4tm2.1Cxd Tg(KRT5-cre)1Xya/0
(involves: 129P2/OlaHsd * 129S6/SvEvTac)
|
increased keratinocyte proliferation
|
J:101602
|
Ptentm2Mak/Ptentm2Mak Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129P2/OlaHsd * C57BL/6 * DBA)
|
increased hepatocyte proliferation
|
J:138099
|
Ptentm2Mak/Ptentm2Mak Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * DBA)
|
abnormal cellular cholesterol metabolism
|
J:90905
|
increased hepatocyte proliferation
|
J:90905
|
oxidative stress
|
J:90905
|
Ptentm2Mak/Ptentm2Mak Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-cre)1Jaw/0
(involves: 129 * 129P2/OlaHsd * C57BL/6 * C57BL/6J)
|
increased mesenchymal cell proliferation involved in lung development
|
J:127405
|
Ptf1atm1(cre)Hnak/Ptf1a+ Rbpjtm1Rsch/Rbpjtm1Rsch
(involves: 129X1/SvJ)
|
abnormal pancreatic alpha cell differentiation
|
J:139250
|
Ptf1atm1.1(cre)Cvw/CbllTg(Alb-KL)7-2Mhos
(involves: C57BL/6)
|
abnormal Purkinje cell differentiation
|
J:100997
|
Ptf1atm2Macd/Ptf1atm2Macd
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal neuron differentiation
|
J:130251
|
Ptgdrtm1Sna/Ptgdrtm1Sna
(B6.129P2-Ptgdrtm1Sna/Sna)
|
decreased mast cell degranulation
|
J:197334
|
Ptgdstm1Ohy/Ptgdstm1Ohy
(B6.129P2-Ptgdstm1Ohy)
|
decreased mast cell degranulation
|
J:197334
|
Ptger2tm1Rsz/Ptger2tm1Rsz
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal osteoclast differentiation
|
J:77408
|
Ptger2tm1Sna/Ptger2tm1Sna
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal oocyte morphology
|
J:57482
|
Ptger4tm1.1Matb/Ptger4tm1.1Matb Tg(Myh6-cre)2182Mds/0
(involves: 129S6/SvEvTac * FVB/N)
|
cardiac interstitial fibrosis
|
J:158439
|
Ptger4tm1.2Matb/Ptger4tm1.2Matb
(involves: 129S6/SvEvTac * C57BL/6)
|
patent ductus arteriosus
|
J:92301
|
Ptger4tm1Bhk/Ptger4tm1Bhk
(involves: 129P2/OlaHsd * 129S/SvEv)
|
patent ductus arteriosus
|
J:44108
|
Ptger4tm1Bhk/Ptger4tm1Bhk
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
abnormal vascular regression
|
J:44108
|
Ptger4tm1Matb/Ptger4tm1Matb
(involves: 129S6/SvEvTac * C57BL/6)
|
patent ductus arteriosus
|
J:92301
|
Ptger4tm1Sna/Ptger4tm1Sna
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:63070
|
decreased T cell proliferation
|
J:83725
|
patent ductus arteriosus
|
J:47618
|
Ptges3tm1Nkt/Ptges3tm1Nkt
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased fibroblast proliferation
|
J:125188
|
Ptgestm1Aki/Ptgestm1Aki
(involves: 129X1/SvJ * C57BL/6)
|
impaired macrophage chemotaxis
|
J:91821
|
Ptgs1tm1Unc/Ptgs1+ Ptgs2tm1Unc/Ptgs2tm1Unc
(involves: 129P2/OlaHsd * C57BL/6J)
|
patent ductus arteriosus
|
J:67208
|
Ptgs1tm1Unc/Ptgs1tm1Unc
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:117986
|
Ptgs1tm1Unc/Ptgs1tm1Unc
(involves: 129P2/OlaHsd * C57BL/6J)
|
maternal effect
|
J:144423
|
Ptgs1tm1Unc/Ptgs1tm1Unc
(involves: 129P2/OlaHsd)
|
increased cellular sensitivity to gamma-irradiation
|
J:108679
|
increased small intestinal crypt cell apoptosis
|
J:108679
|
Ptgs1tm1Unc/Ptgs1tm1Unc Ptgs2tm1.1Fun/Ptgs2tm1.1Fun
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6)
|
patent ductus arteriosus
|
J:109548
|
Ptgs1tm1Unc/Ptgs1tm1Unc Ptgs2tm1Unc/Ptgs2tm1Unc
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
patent ductus arteriosus
|
J:64073
|
Ptgs1tm1Unc/Ptgs1tm1Unc Ptgs2tm1Unc/Ptgs2tm1Unc
(involves: 129P2/OlaHsd * C57BL/6J)
|
patent ductus arteriosus
|
J:67208
|
Ptgs2tm1Jed/Ptgs2tm1Jed
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal primary polar body morphology
|
J:43609
|
patent ductus arteriosus
|
J:109548
|
Ptgs2tm1Unc/Ptgs2+
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:124756
|
Ptgs2tm1Unc/Ptgs2tm1Unc
(involves: 129P2/OlaHsd * C57BL/6J)
|
impaired granulosa cell differentiation
|
J:55145
|
patent ductus arteriosus
|
J:67208
|
Ptgs2tm1Unc/Ptgs2tm1Unc
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:124756
|
Ptgs2tm1Unc/Ptgs2tm1Unc
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:117986
|
Ptgs2tm1Unc/Ptgs2tm1Unc
(B6.129P2-Ptgs2tm1Unc)
|
decreased susceptibility to neuronal excitotoxicity
|
J:67211
|
Ptgs2tm1Unc/Ptgs2tm1Unc
(B6;129P2-Ptgs2tm1Unc/Tac)
|
increased susceptibility to neuronal excitotoxicity
|
J:141610
|
Pth1rtm1Abas/Pth1rtm1Abas
(B6.Cg-Pth1rtm1Abas)
|
abnormal osteoblast physiology
|
J:113660
|
Pth2tm1Vlcg/Pth2tm1Vlcg
(involves: 129 * C57BL/6)
|
abnormal meiosis
|
J:138142
|
decreased spermatid number
|
J:138142
|
Pthtm1Dgo/Pthtm1Dgo
(involves: 129S2/SvPas * C57BL/6J)
|
increased osteoblast apoptosis
|
J:76407
|
increased osteocyte apoptosis
|
J:76407
|
Pthtm1Dgo/Pthtm1Dgo Pthlhtm1Hmk/Pthlhtm1Hmk
(involves: 129S2/SvPas * C57BL/6J)
|
increased chondrocyte apoptosis
|
J:76407
|
increased osteoblast apoptosis
|
J:76407
|
increased osteocyte apoptosis
|
J:76407
|
Pthlhtm1Hmk/Pthlh+
(involves: 129S2/SvPas)
|
abnormal osteoblast differentiation
|
J:100918
|
Pthlhtm1Hmk/Pthlhtm1Hmk
(involves: 129S2/SvPas * C57BL/6J)
|
increased chondrocyte apoptosis
|
J:76407
|
increased osteoblast apoptosis
|
J:76407
|
increased osteocyte apoptosis
|
J:76407
|
Pthlhtm1Hmk/Pthlhtm1Hmk
(involves: 129S2/SvPas * C57BL/6)
|
abnormal mesenchymal cell differentiation involved in lung development
|
J:90274
|
Pthlhtm2Ack/Pthlhtm2Ack
(involves: 129S2/SvPas * C57BL/6)
|
abnormal autophagy
|
J:142669
|
decreased cell proliferation
|
J:142669
|
decreased chondrocyte proliferation
|
J:142669
|
increased apoptosis
|
J:142669
|
Ptk2tm1.1Guan/Ptk2tm1.1Guan Tg(Tek-cre)12Flv/0
(involves: 129P2/OlaHsd * C3H * C57BL/6)
|
increased apoptosis
|
J:162690
|
Ptk2tm1.1Itl/Ptk2tm1.1Itl
(involves: 129S/SvEv * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:165360
|
abnormal fibroblast migration
|
J:165360
|
Ptk2tm1Gwm/Ptk2tm1Gwm Tg(KRT14-cre/ERT2)1Ipc/0
(involves: 129P2/OlaHsd * FVB)
|
decreased keratinocyte migration
|
J:94680
|
increased keratinocyte apoptosis
|
J:94680
|
Ptk2tm1Heen/Ptk2tm1Heen
(involves: 129/Sv * C57BL/6)
|
decreased fibroblast cell migration
|
J:157804
|
decreased fibroblast proliferation
|
J:157804
|
Ptk2tm1Imeg/Ptk2tm1Imeg
(involves: C57BL/6 * CBA)
|
abnormal cell migration
|
J:29273
|
abnormal cell morphology
|
J:29273
|
Ptk2tm1Lfr/Ptk2tm1Ilic Tg(KRT5-cre)5132Jlj/0
(involves: 129X1/SvJ * C57BL/6 * CBA * DBA/2J)
|
decreased keratinocyte proliferation
|
J:107206
|
Ptk2tm1Lfr/Ptk2tm1Lfr Tg(Tek-cre)1Rwng/0
(involves: 129X1/SvJ * FVB/N)
|
abnormal vascular regression
|
J:104401
|
Ptk2tm2.1Guan/Ptk2tm1.1Guan Tg(Tek-cre)12Flv/0
(involves: 129P2/OlaHsd * C3H * C57BL/6 * FVB/N)
|
increased apoptosis
|
J:162690
|
Ptk2btm1Okig/Ptk2btm1Okig
(involves: C57BL/6)
|
abnormal vascular endothelial cell migration
|
J:139849
|
Ptk2btm1Schl/Ptk2btm1Schl
(involves: 129S1/Sv * 129X1/SvJ)
|
impaired macrophage chemotaxis
|
J:99741
|
Ptk7Gt(Betageo)1Matl/Ptk7Gt(Betageo)1Matl
(involves: 129P2/Ola)
|
abnormal outer hair cell kinocilium location or orientation
|
J:91298
|
Ptmatm1.1Got/Ptma+
(involves: C57BL/6J * C57BL/6NTac)
|
abnormal neuron differentiation
|
J:240549
|
abnormal neuron proliferation
|
J:240549
|
Ptntm1Tmu/Ptntm1Tmu
(B6.Cg-Ptntm1Tmu)
|
impaired macrophage chemotaxis
|
J:102069
|
Ptp4a1Gt(CC0606)Wtsi/Ptp4a1+ Ptp4a2Gt(AQ0673)Wtsi/Ptp4a2Gt(AQ0673)Wtsi
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal male germ cell morphology
|
J:250112
|
increased male germ cell apoptosis
|
J:250112
|
oligozoospermia
|
J:250112
|
teratozoospermia
|
J:250112
|
Ptp4a1Gt(CC0606)Wtsi/Ptp4a1Gt(CC0606)Wtsi Ptp4a2Gt(AQ0673)Wtsi/Ptp4a2+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal male germ cell morphology
|
J:250112
|
increased male germ cell apoptosis
|
J:250112
|
oligozoospermia
|
J:250112
|
teratozoospermia
|
J:250112
|
Ptp4a2Gt(AQ0673)Wtsi/Ptp4a2Gt(AQ0673)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal male germ cell physiology
|
J:209512
|
decreased cell proliferation
|
J:190411
|
decreased male germ cell number
|
J:250112,
J:209512
|
increased male germ cell apoptosis
|
J:250112,
J:209512
|
oligozoospermia
|
J:250112,
J:209512
|
Ptpmt1tm1.1Jedi/Ptpmt1tm1.1Jedi
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal aerobic respiration
|
J:176087
|
abnormal cell physiology
|
J:176087
|
abnormal mitochondrial morphology
|
J:176087
|
decreased cell proliferation
|
J:176087
|
Ptpmt1tm1Ckq/Ptpmt1tm1Ckq
(B6.Cg-Ptpmt1tm1Ckq)
|
absent inner cell mass proliferation
|
J:178313
|
increased embryonic tissue cell apoptosis
|
J:178313
|
Ptpmt1tm2.1Ckq/Ptpmt1tm2.1Ckq Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal aerobic respiration
|
J:194929
|
Ptpn2tm1.1Kry/Ptpn2tm1.1Kry Tg(Col1a1-cre)1Kry/0
(involves: 129 * C57BL/6J * FVB)
|
abnormal osteoclast differentiation
|
J:183709
|
Ptpn6me/Ptpn6me
(C57BL/6J-Ptpn6me/J)
|
abnormal cell cycle
|
J:66843
|
abnormal cell cycle checkpoint function
|
J:66843
|
decreased apoptosis
|
J:66843
|
decreased cellular sensitivity to gamma-irradiation
|
J:66843
|
Ptpn6me/Ptpn6me
(involves: C3H/HeN * C57BL/6J * NFS)
|
increased splenocyte proliferation
|
J:30994
|
Ptpn9tm1Dny/Ptpn9tm1Dny
(B6.129-Ptpn9tm1Dny)
|
decreased T cell proliferation
|
J:118880
|
Ptpn11tm1.1Ics/Ptpn11+
(involves: 129S2/SvPas * C57BL/6 * FVB/N)
|
abnormal fat cell differentiation
|
J:216593
|
increased adipocyte glucose uptake
|
J:216593
|
Ptpn11tm1.1Wbm/Ptpn11tm1.1Wbm H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL * SJL/J)
|
abnormal axon extension
|
J:153219
|
abnormal axon fasciculation
|
J:153219
|
Ptpn11tm1Bgn/Ptpn11+
(involves: 129S4/SvJae * C57BL/6J)
|
decreased cardiomyocyte apoptosis
|
J:91609
|
increased cell proliferation
|
J:91609
|
Ptpn11tm1Bgn/Ptpn11tm1Bgn
(involves: 129S4/SvJae * C57BL/6J)
|
decreased cardiomyocyte apoptosis
|
J:91609
|
increased cell proliferation
|
J:91609
|
Ptpn11tm1Ckq/Ptpn11+ Tg(Mx1-cre)1Cgn/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA)
|
aneuploidy
|
J:177285
|
chromosomal instability
|
J:177285
|
Ptpn11tm1Gsf/Ptpn11tm1Gsf Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal spermatocyte morphology
|
J:250152
|
abnormal spermatogonia morphology
|
J:250152
|
azoospermia
|
J:250152
|
decreased male germ cell number
|
J:250152
|
increased male germ cell apoptosis
|
J:250152
|
Ptpn11tm1Gsf/Ptpn11tm1Gsf Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA)
|
increased hepatocyte proliferation
|
J:172422
|
Ptpn11tm1Gsf/Ptpn11tm1Gsf Tg(Ckmm-cre)5Khn/0
(involves: 129S1/Sv * 129X1/SvJ * FVB)
|
decreased cardiac muscle cell glucose uptake
|
J:144767
|
decreased skeletal muscle cell glucose uptake
|
J:144767
|
Ptpn11tm1Paw/Ptpn11tm1Paw
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell death
|
J:106624
|
decreased cell proliferation
|
J:106624
|
polyploidy
|
J:106624
|
Ptpn11tm5Bgn/Ptpn11tm5Bgn
(involves: 129S4/SvJae * C57BL/6J)
|
decreased trophectoderm cell proliferation
|
J:106624
|
Ptpn12tm1Vei/Ptpn12tm1Vei Tg(Cd4-cre)1Cwi/0
(B6.Cg-Tg(Cd4-cre)1Cwi Ptpn12tm1Vei)
|
decreased T cell proliferation
|
J:163910
|
Ptpn13tm1Gru/Ptpn13tm1Gru
(involves: C57BL/6)
|
abnormal cell physiology
|
J:118426
|
Ptpn22tm1.1Draw/Ptpn22+
(involves: 129 * C57BL/6)
|
decreased B cell apoptosis
|
J:201448
|
increased B cell proliferation
|
J:201448
|
increased T cell proliferation
|
J:201448
|
Ptpn22tm1.1Draw/Ptpn22tm1.1Draw
(involves: 129 * C57BL/6)
|
decreased B cell apoptosis
|
J:201448
|
increased B cell proliferation
|
J:201448
|
increased T cell proliferation
|
J:201448
|
Ptpn22tm1.1Kas/Ptpn22tm1.1Kas
(involves: C57BL/6)
|
increased B cell proliferation
|
J:176519
|
increased T cell proliferation
|
J:176519
|
Ptpn22tm1.1Kas/Ptpn22tm1.1Kas Tg(TcraTcrb)425Cbn/0
(involves: BALB/c * C57BL/6)
|
increased T cell proliferation
|
J:176519
|
Ptpratm1Sap/Ptpratm1Sap
(involves: 129S6/SvEvTac * 129X1/SvJ)
|
abnormal cell adhesion
|
J:55040
|
abnormal cell physiology
|
J:55040
|
Ptprbtm1Gdy/Ptprbtm1Gdy
(involves: 129 * C57BL/6)
|
abnormal vascular regression
|
J:125903
|
Ptprctm1Mak/Ptprctm1Mak
(involves: 129/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:13163
|
decreased T cell proliferation
|
J:13163
|
Ptprctm1Mak/Ptprctm1Mak
(involves: 129)
|
decreased mast cell degranulation
|
J:110782
|
Ptprctm1Mak/Ptprctm1Mak
(B6.Cg-Ptprctm1Mak)
|
increased T cell apoptosis
|
J:111646
|
Ptprctm1Mak/Ptprctm1Mak Ptprjtm1.2Weis/Ptprjtm1.2Weis
(involves: 129/Sv * 129P2/OlaHsd * BALB/cJ * C57BL/6)
|
impaired macrophage phagocytosis
|
J:131736
|
Ptprctm1Weis/Ptprctm1Weis
(involves: 129X1/SvJ * C57BL/6)
|
abnormal granulocyte differentiation
|
J:66501
|
Ptprcaptm1Tkda/Ptprcaptm1Tkda
(involves: 129X1/SvJ)
|
decreased B cell proliferation
|
J:48387
|
decreased T cell proliferation
|
J:48387
|
Ptpretm1Ael/Ptpretm1Ael
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal osteoclast differentiation
|
J:90031
|
PtprfGt(ST534)Byg/PtprfGt(ST534)Byg
(D.129P2-PtprfGt(ST534)Byg)
|
abnormal cell differentiation
|
J:108603
|
abnormal neuron differentiation
|
J:108603
|
increased cell proliferation
|
J:108603
|
Ptprstm1Mtr/Ptprstm1Mtr
(involves: BALB/c)
|
abnormal axon extension
|
J:85382
|
Ptprtm1Rgsc/Ptprtm1Rgsc
(C57BL/6J-Ptprtm1Rgsc)
|
impaired neuron differentiation
|
J:298303
|
Ptprttm1Sata/Ptprttm1Sata
(involves: 129P2/OlaHsd)
|
impaired neuron differentiation
|
J:298303
|
Ptprvtm1Asmi/Ptprvtm1Asmi
(involves: 129P2/OlaHsd)
|
abnormal male germ cell apoptosis
|
J:170888
|
Ptprvtm1Asmi/Ptprvtm1Asmi
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased pancreatic beta cell proliferation
|
J:152695
|
Ptprvtm1Kry/Ptprvtm1Kry Tg(Col1a1-cre)1Kry/0
(involves: FVB)
|
abnormal muscle fiber mitochondrial morphology
|
J:126780
|
increased adipocyte glucose uptake
|
J:126780
|
increased muscle cell glucose uptake
|
J:126780
|
increased pancreatic beta cell proliferation
|
J:126780
|
Ptrh2tm1.1Eruo/Ptrh2tm1.1Eruo
(C57BL/6-Ptrh2tm1.1Eruo)
|
decreased fibroblast apoptosis
|
J:131853
|
Pttg1tm1Pzg/Pttg1tm1Pzg
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:121688
|
decreased cell proliferation
|
J:121688
|
Pttg1tm1Sme/Pttg1tm1Sme
(involves: 129S4/SvJae * C57BL/6)
|
decreased pancreatic beta cell proliferation
|
J:82724
|
Ptx3tm1Mant/Ptx3tm1Mant
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
impaired macrophage phagocytosis
|
J:85080
|
Pum1tm1.1Hfl/Pum1tm1.2Hfl Tg(Ddx4-cre)1Dcas/0
(involves: 129 * C57BL/6 * FVB)
|
increased male germ cell apoptosis
|
J:182280
|
Pum1tm1.2Hfl/Pum1+
(involves: 129 * C57BL/6 * FVB)
|
increased male germ cell apoptosis
|
J:182280
|
oligozoospermia
|
J:182280
|
Pum1tm1.2Hfl/Pum1tm1.2Hfl
(involves: 129 * C57BL/6 * FVB)
|
increased male germ cell apoptosis
|
J:182280
|
oligozoospermia
|
J:182280
|
Puratm1Herm/Pura+
(involves: 129P2/OlaHsd * BALB/c)
|
abnormal neuron proliferation
|
J:179606
|
Puratm1Herm/Puratm1Herm
(involves: 129P2/OlaHsd * BALB/c)
|
abnormal neuron proliferation
|
J:179606
|
Puratm1Kkh/Pura+
(involves: 129)
|
decreased cell proliferation
|
J:85759
|
decreased DNA replication
|
J:85759
|
Puratm1Kkh/Puratm1Kkh
(involves: 129)
|
decreased cell proliferation
|
J:85759
|
decreased DNA replication
|
J:85759
|
decreased neuronal precursor proliferation
|
J:85759
|
Pus1tm1.1Mdf/Pus1tm1.1Mdf
(B6.129S7(C)-Pus1tm1.1Mdf)
|
decreased mitochondrial size
|
J:237107
|
Pvalbtm1Swal/Pvalbtm1Swal
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:113147
|
abnormal Purkinje cell mitochondrial morphology
|
J:113147
|
Pxdnmhdakta048/Pxdnmhdakta048
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal extracellular matrix morphology
|
J:213336
|
decreased cell proliferation
|
J:213336
|
Pxntm1Smth/Pxntm1Smth
(either: (involves: 129S4/SvJaeSor * C57BL/6) or (involves: 129/Sv))
|
cellular phenotype
|
J:73970
|
Pycr2tm1.1Brre/Pycr2tm1.1Brre
(involves: C57BL/6)
|
abnormal oligodendrocyte apoptosis
|
J:296329
|
impaired neuron differentiation
|
J:296329
|
increased neuron apoptosis
|
J:296329
|
Pygo1tm1.1Kba/Pygo1tm1.1Kba Pygo2tm1.1Kba/Pygo2tm1.1Kba
(involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NTac)
|
abnormal spermatid morphology
|
J:198562
|
oligozoospermia
|
J:198562
|
Pygo2tm1.1Xdai/Pygo2tm1.2Xdai Tg(KRT14-cre)#Smr/0
(involves: 129P2/OlaHsd * C57BL/6J * SJL/J)
|
decreased mammary gland epithelial cell proliferation
|
J:163218
|
Pygo2tm1.2Xdai/Pygo2tm1.2Xdai
(involves: 129P2/OlaHsd)
|
decreased mammary gland epithelial cell proliferation
|
J:163218
|
Qdprtm1Lex/Qdprtm1Lex
(involves: 129S/SvEvBrd * C57BL/6J)
|
oxidative stress
|
J:216352
|
Qkiqk-v/Qkiqk-v
(B6C3Fe a/a-Qkiqk-v/J)
|
abnormal sperm flagellum morphology
|
J:88151
|
abnormal sperm head morphology
|
J:88151
|
necrospermia
|
J:88151
|
oligozoospermia
|
J:88151
|
Qkiqk-v/Qkiqk-v Tg(PGK2-Pacrg)#Jus/?
(involves: BTBR * C57BL/6J * DBA/2)
|
oligozoospermia
|
J:90667
|
QprtGt(OST337946)Lex/QprtGt(OST337946)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal mitochondrial morphology
|
J:282516
|
abnormal oxidative phosphorylation
|
J:282516
|
Qrich2em1Xdz/Qrich2+
(involves: C57BL/6J)
|
asthenozoospermia
|
J:270177
|
decreased sperm progressive motility
|
J:270177
|
oligozoospermia
|
J:270177
|
Qrich2em1Xdz/Qrich2em1Xdz
(involves: C57BL/6J)
|
abnormal outer dense fiber morphology
|
J:270177
|
abnormal sperm axoneme morphology
|
J:270177
|
abnormal sperm flagellum morphology
|
J:270177
|
abnormal sperm midpiece morphology
|
J:270177
|
abnormal sperm principal piece morphology
|
J:270177
|
absent sperm flagellum
|
J:270177
|
asthenozoospermia
|
J:270177
|
coiled sperm flagellum
|
J:270177
|
decreased sperm progressive motility
|
J:270177
|
kinked sperm flagellum
|
J:270177
|
oligozoospermia
|
J:270177
|
short sperm flagellum
|
J:270177
|
Qtrt1Gt(S12-11A1)Sor/Qtrt1+
(involves: 129S4/SvJaeSor)
|
abnormal cell physiology
|
J:173496
|
Qtrt1Gt(S12-11A1)Sor/Qtrt1Gt(S12-11A1)Sor
(involves: 129S4/SvJaeSor)
|
abnormal cell physiology
|
J:173496
|
R3hdmltm1Mita/R3hdmltm1Mita
(B6.Cg-R3hdmltm1Mita)
|
abnormal skeletal muscle satellite cell proliferation
|
J:282737
|
Rab7em2Rwb/Rab7+
(C57BL/6J-Rab7em2Rwb/RwbJ)
|
abnormal lysosome morphology
|
J:346904
|
abnormal lysosome physiology
|
J:346904
|
abnormal mitochondrial physiology
|
J:346904
|
abnormal neuron mitochondrial morphology
|
J:346904
|
Rab7tm1.1Ale/Rab7tm1.1Ale Tg(Cd4-cre)1Cwi/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal autophagy
|
J:211733
|
decreased T cell proliferation
|
J:211733
|
increased mitochondrial size
|
J:211733
|
oxidative stress
|
J:211733
|
Rab7btm1Ciphe/Rab7btm1Ciphe Tg(Itgax-cre)1-1Reiz/0
(involves: C57BL/6N * CBA)
|
abnormal dendritic cell migration
|
J:321707
|
abnormal lysosome morphology
|
J:321707
|
Rab8atm1.2Aha/Rab8atm1.2Aha
(involves: C57BL/6 * SJL)
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:123415
|
Rab8atm1.2Aha/Rab8atm1.2Aha Rab8btm1.2Aha/Rab8btm1.2Aha
(involves: BALB/cJ * C57BL/6 * SJL)
|
cellular phenotype
|
J:211898
|
Rab8atm1Aha/Rab8atm1Aha
(Not Specified)
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:123415
|
Rab10tm1c(KOMP)Wtsi/Rab10tm1c(KOMP)Wtsi Tg(Adipoq-cre)1Evdr/0
(involves: C57BL/6J * C57BL/6N * FVB/NJ)
|
decreased adipocyte glucose uptake
|
J:249843
|
Rab10tm1Tax/Rab10tm1Tax
(B6.Cg-Rab10tm1Tax)
|
abnormal cell nucleus morphology
|
J:262459
|
abnormal vacuole morphology
|
J:262459
|
decreased cell proliferation
|
J:262459
|
Rab11atm1.1Ngao/Rab11atm1.1Ngao Tg(Vil1-cre)997Gum/0
(involves: 129S4/SvJae * C57BL/6J * SJL)
|
abnormal intestinal goblet cell morphology
|
J:215917
|
abnormal small intestinal crypt cell proliferation
|
J:215917
|
Rab11atm1.1Ngao/Rab11atm1.1Ngao Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129S4/SvJae * C57BL/6 * DBA/2)
|
abnormal small intestinal crypt cell proliferation
|
J:278932,
J:215917
|
Rab13tm1.1Ktg/Rab13tm1.1Ktg
(involves: C57BL/6)
|
abnormal leukocyte adhesion
|
J:259093
|
decreased lymphocyte chemotaxis
|
J:259093
|
impaired leukocyte migration
|
J:259093
|
Rab18Gt(EUCE0233a03)Hmgu/Rab18Gt(EUCE0233a03)Hmgu
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cytoskeleton morphology
|
J:211808
|
Rab27aash-N/Rab27aash-N
(B10.F)
|
cellular phenotype
|
J:7366
|
Rab27aash/Rab27aash
(involves: C3H/HeDiSn)
|
abnormal NK cell degranulation
|
J:111253
|
abnormal vesicle-mediated transport
|
J:134370
|
Rab27aash/Rab27aash
(B6.C3Sn-Rab27aash)
|
decreased NK cell degranulation
|
J:193137
|
Rab27aash/Rab27aash
(C3H/HeSn-Rab27aash/J)
|
decreased platelet ATP level
|
J:77395
|
Rab29tm1b(EUCOMM)Wtsi/Rab29tm1b(EUCOMM)Wtsi
(involves: BALB/cJ * C57BL/6J * C57BL/6N)
|
abnormal Golgi vesicle transport
|
J:314451
|
abnormal vesicle-mediated transport
|
J:314451
|
accumulation of giant lysosomes in kidney/renal tubule cells
|
J:314451
|
Rab32tm1b(KOMP)Wtsi/Rab32+ Rab38tm1.1Ics/Rab38tm1.1Ics
(involves: C57BL/6N * C57BL/6NTac)
|
decreased platelet ATP level
|
J:293385
|
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi Rab38tm1.1Ics/Rab38+
(involves: C57BL/6N * C57BL/6NTac)
|
decreased platelet ATP level
|
J:293385
|
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi Rab38tm1.1Ics/Rab38tm1.1Ics
(involves: C57BL/6N * C57BL/6NTac)
|
decreased platelet ATP level
|
J:293385
|
Rab33bem1Rmr/Rab33b+
(involves: C57BL/6)
|
abnormal osteoclast differentiation
|
J:338833
|
Rabggtagm/Rabggtagm
(C57BL/6J-Rabggtagm)
|
abnormal megakaryocyte differentiation
|
J:12434
|
Rabl2mot/Rabl2mot
(involves: C57BL/6 * CBA)
|
asthenozoospermia
|
J:193640
|
oligozoospermia
|
J:193640
|
short sperm flagellum
|
J:193640
|
Rac1tm1Djk/Rac1tm1.1Djk Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:83457
|
Rac1tm1Djk/Rac1tm1.1Djk Tg(Myh6-cre/Esr1*)1Liao/0
(involves: 129S4/SvJae * C57BL/6)
|
oxidative stress
|
J:109582
|
Rac1tm1Djk/Rac1tm1Djk Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+ Tg(Mef2c-cre)2Blk/0
(involves: 129 * BALB/c * C57BL/6 * C57BL/6J)
|
decreased cell migration
|
J:315097
|
Rac1tm1Djk/Rac1tm1Djk Tg(Mef2c-cre)2Blk/0
(involves: 129S4/SvJae * BALB/c * C57BL/6)
|
abnormal cell adhesion
|
J:315097
|
increased apoptosis
|
J:315097
|
Rac1tm1Djk/Rac1tm1Djk Tg(Nkx2-5-cre)9Eno/0
(involves: 129S4/SvJae * BALB/c * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:321017
|
Rac1tm1Jms/Rac1tm1Jms
(involves: 129S/SvEv * C57BL/6J)
|
increased apoptosis
|
J:52224
|
Rac1tm1Tyb/Rac1tm2Tyb Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S4/SvJae * C3H * C57BL/6 * CBA)
|
abnormal cell adhesion
|
J:173526
|
decreased cell proliferation
|
J:173526
|
increased embryonic tissue cell apoptosis
|
J:173526
|
Rac1tm1Tyb/Rac1tm2Tyb Tg(Ttr-cre)1Hadj/0
(involves: 129S4/SvJae * C3H * C57BL/6 * CBA/J)
|
abnormal anterior visceral endoderm cell migration
|
J:166095
|
Rac1tm2Tyb/Rac1tm2Tyb
(involves: 129S4/SvJae * C3H * C57BL/6 * CD-1)
|
abnormal anterior visceral endoderm cell migration
|
J:166095
|
Rac1tm2Tyb/Rac1tm2Tyb Tg(Hhex-EGFP)#Rbe/0
(mixed)
|
abnormal anterior visceral endoderm cell migration
|
J:166095
|
Rac2em1Shl/Rac2+
(involves: C57BL/6)
|
oxidative stress
|
J:276213
|
Rac2tm1Mddw/Rac2tm1Mddw
(involves: 129S/SvEv * C57BL/6)
|
abnormal granulocyte differentiation
|
J:53362
|
decreased T cell proliferation
|
J:119437
|
impaired neutrophil chemotaxis
|
J:53362
|
Rac2tm1Mddw/Rac2tm1Mddw
(involves: 129S/SvEv)
|
decreased vascular endothelial cell proliferation
|
J:131305
|
Rac2tm1Mddw/Rac2tm1Mddw Tg(TcrAND)53Hed/0
(involves: 129S/SvEv * C57BL/6 * SJL)
|
decreased T cell proliferation
|
J:119437
|
Racgap1tm1Mahi/Racgap1tm1Mahi Tg(Stra8-icre)1Reb/0
(involves: C57BL/6 * FVB/NJ)
|
abnormal spermatogonia morphology
|
J:206583
|
abnormal spermatogonia proliferation
|
J:206583
|
azoospermia
|
J:206583
|
decreased male germ cell number
|
J:206583
|
decreased spermatogonia number
|
J:206583
|
multinucleated giant male germ cells
|
J:206583
|
Rack1tm1Sbif/Rack1+
(C57BL/6-Rack1tm1Sbif)
|
abnormal translation
|
J:223207
|
Rad9atm2Lieb/Rad9a+ Tg(KRT5-cre)1Xya/?
(involves: 129S/SvEv * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:138845
|
Rad9atm2Lieb/Rad9atm2Lieb Tg(KRT5-cre)1Xya/?
(involves: 129S/SvEv * C57BL/6)
|
abnormal cell cycle
|
J:138845
|
abnormal double-strand DNA break repair
|
J:138845
|
increased apoptosis
|
J:138845
|
Rad9btm1Lieb/Rad9b+
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased cellular sensitivity to gamma-irradiation
|
J:165426
|
increased sensitivity to induced cell death
|
J:165426
|
Rad9btm1Lieb/Rad9btm1Lieb
(involves: 129S6/SvEvTac * C57BL/6J)
|
cellular phenotype
|
J:165426
|
early cellular replicative senescence
|
J:165426
|
increased cellular sensitivity to gamma-irradiation
|
J:165426
|
increased sensitivity to induced cell death
|
J:165426
|
Rad18tm1a(EUCOMM)Wtsi/Rad18tm1a(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
chromosomal instability
|
J:213427
|
Rad18tm1Stat/Rad18tm1Stat
(B6.Cg-Rad18tm1Stat)
|
abnormal spermatogonia morphology
|
J:145534
|
decreased male germ cell number
|
J:145534
|
Rad21tm1.1Kktk/Rad21tm1.1Kktk
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal female meiosis
|
J:166151
|
Rad21ltm1Amp/Rad21ltm1Amp
(involves: 129S6/SvEvTac * C57BL/6NCr)
|
abnormal double-strand DNA break repair
|
J:176168
|
abnormal female meiosis
|
J:176168
|
abnormal male germ cell apoptosis
|
J:176168
|
abnormal male meiosis
|
J:176168
|
abnormal synaptonemal complex
|
J:176168
|
abnormal telomere morphology
|
J:176168
|
arrest of male meiosis
|
J:176168
|
azoospermia
|
J:176168
|
decreased oocyte number
|
J:176168
|
Rad21ltm1Amp/Rad21ltm1Amp
(B6.Cg-Rad21ltm1Amp)
|
abnormal male meiosis
|
J:205574
|
Rad21ltm1b(KOMP)Wtsi/Rad21ltm1b(KOMP)Wtsi
(B6N(Cg)-Rad21ltm1b(KOMP)Wtsi)
|
cellular phenotype
|
J:280261
|
Rad21ltm1b(KOMP)Wtsi/Rad21ltm1b(KOMP)Wtsi Rec8tm1b(KOMP)Wtsi/Rec8tm1b(KOMP)Wtsi
(B6N(Cg)-Rad21ltm1b(KOMP)Wtsi Rec8tm1b(KOMP)Wtsi)
|
abnormal double-strand DNA break repair
|
J:280261
|
Rad21ltm1b(KOMP)Wtsi/Rad21ltm1b(KOMP)Wtsi Stag3tm1e.1(KOMP)Wtsi/Stag3tm1e.1(KOMP)Wtsi
(B6N(Cg)-Rad21ltm1b(KOMP)Wtsi Stag3tm1e.1(KOMP)Wtsi)
|
abnormal double-strand DNA break repair
|
J:280261
|
abnormal synaptonemal complex
|
J:280261
|
Rad21ltm1Yow/Rad21ltm1Yow
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal chromosomal synapsis
|
J:209347
|
abnormal female meiosis
|
J:209347
|
abnormal male meiosis
|
J:209347
|
abnormal meiosis
|
J:209347
|
abnormal synaptonemal complex
|
J:209347
|
absent oocytes
|
J:209347
|
arrest of male meiosis
|
J:209347
|
Rad21ltm1Yow/Rad21ltm1Yow Rec8mei8/Rec8mei8
(involves: 129S4/SvJae * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal male meiosis
|
J:209347
|
abnormal meiosis
|
J:209347
|
Rad21ltm1Yow/Rad21ltm1Yow Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal chromosomal synapsis
|
J:209347
|
abnormal male meiosis
|
J:209347
|
abnormal synaptonemal complex
|
J:209347
|
Rad21ltm1Yow/Rad21ltm1Yow Sun1tm1Mhan/Sun1tm1Mhan
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal chromosomal synapsis
|
J:209347
|
abnormal male meiosis
|
J:209347
|
Rad23atm1Jhjh/Rad23atm1Jhjh Rad23btm1Gvh/Rad23btm1Gvh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal DNA repair
|
J:84299
|
Rad50tm1Jpt/Rad50tm1Jpt
(involves: 129S7/SvEvBrd)
|
decreased cell proliferation
|
J:56083
|
increased cellular sensitivity to gamma-irradiation
|
J:56083
|
Rad50tm1Jpt/Rad50tm3Jpt Tg(Mx1-cre)1Cgn/0
(involves: 129S7/SvEvBrd * C57BL/6 * CBA)
|
decreased hepatocyte proliferation
|
J:144766
|
Rad50tm2.1Flv/Rad50tm2.2Flv Tg(Cd4-cre)1Cwi/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2)
|
abnormal DNA methylation
|
J:165055
|
Rad51tm1Csha/Rad51tm1Csha Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
(involves: 129S/Sv * C57BL/6J)
|
abnormal double-strand DNA break repair
|
J:324159
|
abnormal male meiosis
|
J:324159
|
abnormal spermatocyte morphology
|
J:324159
|
decreased male germ cell number
|
J:324159
|
increased male germ cell apoptosis
|
J:324159
|
Rad51tm1Csha/Rad51tm1Csha Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6J * FVB)
|
abnormal male meiosis
|
J:324159
|
abnormal spermatocyte morphology
|
J:324159
|
absent spermatogonia
|
J:324159
|
decreased male germ cell number
|
J:324159
|
Rad51tm1Hst/Rad51tm1Hst
(involves: 129S7/SvEvBrd * C57BL/6)
|
absent inner cell mass proliferation
|
J:36540
|
decreased cell proliferation
|
J:36540
|
increased cellular sensitivity to gamma-irradiation
|
J:36540
|
increased embryonic epiblast cell apoptosis
|
J:36540
|
Rad51tm1Hst/Rad51tm1Hst Trp53tm1Brd/Trp53tm1Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased cell proliferation
|
J:36540
|
Rad51ap2em1Qsh/Rad51ap2em1Qsh
(involves: C57BL/6J * DBA/2J)
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:321708
|
arrest of male meiosis
|
J:321708
|
increased male germ cell apoptosis
|
J:321708
|
oligozoospermia
|
J:321708
|
Rad51ap2em2Qsh/Rad51ap2em2Qsh
(involves: C57BL/6J * DBA/2J)
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:321708
|
Rad51ctm1Sks/Rad51ctm1.1Sks
(involves: 129/Sv * C57BL/6J * FVB/N)
|
abnormal female meiosis
|
J:119835
|
abnormal spermatocyte morphology
|
J:119835
|
arrest of male meiosis
|
J:119835
|
oligozoospermia
|
J:119835
|
Rad51dtm1Jcs/Rad51dtm1Jcs
(involves: 129S4/SvJae * C57BL/6J)
|
decreased cellular sensitivity to gamma-irradiation
|
J:61460
|
decreased cellular sensitivity to methylmethanesulfonate
|
J:61460
|
Rad52tm1Aps/Rad52tm1Aps Rad54ltm1Jhjh/Rad54ltm1Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal chromosome morphology
|
J:101697
|
Rad54btm1Roka/Rad54btm1Roka
(involves: 129P2/OlaHsd)
|
increased cellular sensitivity to gamma-irradiation
|
J:105544
|
Rad54btm1Roka/Rad54btm1Roka Rad54ltm1Jhjh/Rad54ltm1Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:105544
|
increased cellular sensitivity to gamma-irradiation
|
J:105544
|
Rad54l2Gt(A016E03)Oaj/Rad54l2Gt(A016E03)Oaj
(involves: ICR)
|
decreased cell proliferation
|
J:121844
|
decreased fibroblast proliferation
|
J:121844
|
increased apoptosis
|
J:121844
|
increased fibroblast apoptosis
|
J:121844
|
increased neural tube apoptosis
|
J:121844
|
Rad54ltm1Jhjh/Rad54ltm1Jhjh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:83373
|
abnormal chromosome morphology
|
J:101697
|
increased cellular sensitivity to gamma-irradiation
|
J:105544
|
Radsvq1C57BL/6JNrs/Radsvq1C57BL/6JNrs
(involves: C3H/HeNrs * C57BL/6JNrs)
|
increased cellular sensitivity to gamma-irradiation
|
J:122918
|
Rae1tm1Jvd/Rae1+
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:81546,
J:105717
|
abnormal mitosis
|
J:81546,
J:105717
|
aneuploidy
|
J:81546,
J:105717
|
Raf1tm1.1Bgn/Raf1+
(involves: 129S6/SvEvTac * C57BL/6NCr)
|
cardiac interstitial fibrosis
|
J:172034
|
Raf1tm1Bacc/Raf1tm1Bacc
(involves: 129P2/OlaHsd * 129/Sv)
|
decreased sensitivity to induced cell death
|
J:69056
|
increased fibroblast apoptosis
|
J:69056
|
increased hepatoblast apoptosis
|
J:69056
|
increased sensitivity to induced cell death
|
J:69056
|
Raf1tm1Bacc/Raf1tm1Bacc
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:69056
|
increased apoptosis
|
J:69056
|
increased fibroblast apoptosis
|
J:69056
|
increased hepatoblast apoptosis
|
J:69056
|
increased sensitivity to induced cell death
|
J:69056
|
Raf1tm1Ulb/Raf1tm1Ulb
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal apoptosis
|
J:89619
|
Raf1tm1Zim/Raf1tm1Zim
(involves: 129/Sv * CD-1)
|
decreased fibroblast proliferation
|
J:50696
|
Raf1tm2Bacc/Raf1tm2Bacc Tg(Mx1-cre)1Cgn/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
increased apoptosis
|
J:93687
|
Raf1tm2Bacc/Raf1tm2Bacc Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6J)
|
increased cardiomyocyte apoptosis
|
J:93418
|
Raf1tm3Ulb/Raf1tm3Ulb
(Not Specified)
|
decreased cell proliferation
|
J:141095
|
increased embryonic tissue cell apoptosis
|
J:141095
|
increased sensitivity to induced cell death
|
J:141095
|
Rag1tm1Fwa/Rag1tm1Fwa Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * 129S6/SvEvTac)
|
cellular phenotype
|
J:170462
|
Rag1tm1Jsek/Rag1tm1Jsek
(involves: 129S6/SvEvTac)
|
spontaneous chromosome breakage
|
J:146912
|
Rag1tm1Jsek/Rag1tm1Jsek Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * 129S6/SvEvTac)
|
spontaneous chromosome breakage
|
J:146912
|
Rag1tm1Mom/Rag1tm1Mom
(involves: 129S7/SvEvBrd)
|
abnormal neuron proliferation
|
J:170591
|
Rag1tm1Mom/Rag1tm1Mom Sh3bp2tm1Bjro/Sh3bp2tm1Bjro
(involves: 129S4/SvJae * 129S7/SvEvBrd * BALB/cJ * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:117880
|
Rag1tm1Mom/Rag1tm1Mom Slc46a2tm1Moki/Slc46a2+ Tg(TcraB12,TcrbB12)1Rest/0
(involves: 129 * C57BL/6)
|
increased T cell apoptosis
|
J:140121
|
Rag1tm1Mom/Rag1tm1Mom Vtcn1tm1Lpc/Vtcn1tm1Lpc
(involves: 129S/SvEvBrd * 129S7/SvEvBrd * C57BL/6)
|
abnormal neutrophil differentiation
|
J:145712
|
Rag2tm1.1Mss/Rag2tm1.1Mss Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * 129S6/SvEvTac)
|
abnormal chromosome morphology
|
J:170462
|
aneuploidy
|
J:170462
|
Rag2tm1Avla/Rag2tm1Avla
(involves: 129/Sv * C57BL/6)
|
decreased T cell proliferation
|
J:122108
|
Rag2tm1Cgn/Rag2tm1Cgn Xrcc4tm1Fwa/Xrcc4tm2Fwa Tg(Cr2-cre)3Cgn/?
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6)
|
spontaneous chromosome breakage
|
J:150339
|
Rag2tm1Fwa/Rag2tm1Fwa Sos1tm1.1Les/Sos1tm1.1Les Tg(Lck-cre)1Cwi/0
(involves: 129S/SvEv * C57BL/6)
|
decreased T cell proliferation
|
J:174536
|
Rag2tm1Fwa/Rag2tm1Fwa Tg(TcrHEL3A9)1Mmd/0
(involves: 129S/SvEv * C57BL/6)
|
abnormal T cell proliferation
|
J:78309
|
Rag2tm1Fwa/Rag2tm1Fwa Tg(TcrHEL3A9)1Mmd/0 Tg(TLK2mHEL)2Ccg/0
(involves: 129S/SvEv * C57BL/6)
|
abnormal T cell proliferation
|
J:78309
|
Ralatm1.1Cjm/Ralatm1.1Cjm
(involves: C57BL/6 * C57BL/6J)
|
cellular phenotype
|
J:199742
|
Ralatm1.2Cjm/Ralatm1.2Cjm Ralbtm1.1Cjm/Ralbtm1.1Cjm
(involves: C57BL/6 * C57BL/6J)
|
decreased fibroblast proliferation
|
J:199742
|
Ralatm1.2Cjm/Ralatm1.2Cjm Ralbtm1.2Cjm/Ralbtm1.2Cjm
(involves: C57BL/6 * C57BL/6J)
|
cellular phenotype
|
J:199742
|
Ralbp1Gt(OST359995)Lex/Ralbp1+
(involves: 129S5/SvEvBrd * C57BL)
|
oxidative stress
|
J:100087
|
Ralbp1Gt(OST359995)Lex/Ralbp1Gt(OST359995)Lex
(involves: 129S5/SvEvBrd * C57BL)
|
oxidative stress
|
J:100087
|
Ralgapa1tm1.1Schen/Ralgapa1tm1.1Schen
(involves: C57BL/6J)
|
decreased muscle cell glucose uptake
|
J:287672
|
Ralgapa1tm2c(KOMP)Wtsi/Ralgapa1tm2c(KOMP)Wtsi Myl1tm1(cre)Sjb/Myl1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N)
|
increased muscle cell glucose uptake
|
J:287672
|
Raml1C57BL/6J/?
(involves: C57BL/6J * CBA/Ca)
|
increased cellular sensitivity to X-ray irradiation
|
J:105074
|
Ranbp1Gt(S17-6E1)1.1Sor/Ranbp1Gt(S17-6E1)1.1Sor
(B6.129S4(129S6)-Ranbp1Gt(S17-6E1)1.1Sor)
|
abnormal cell cycle
|
J:235630
|
abnormal neuron differentiation
|
J:235630
|
abnormal neuronal precursor proliferation
|
J:235630
|
Ranbp1tm1Yyo/Ranbp1tm1Yyo
(involves: 129S2/SvPas * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:170335
|
azoospermia
|
J:170335
|
Ranbp2tm1.1Jvd/Ranbp2+
(involves: 129/Sv * C57BL/6)
|
aneuploidy
|
J:137482
|
Ranbp2tm1Jvd/Ranbp2tm1.1Jvd
(involves: 129/Sv * C57BL/6)
|
abnormal mitosis
|
J:137482
|
aneuploidy
|
J:137482
|
elevated level of mitotic sister chromatid exchange
|
J:137482
|
Ranbp2tm1Jvd/Ranbp2tm1Jvd
(involves: 129/Sv * C57BL/6)
|
abnormal mitosis
|
J:137482
|
aneuploidy
|
J:137482
|
elevated level of mitotic sister chromatid exchange
|
J:137482
|
Ranbp9Gt(RHA056)Byg/Ranbp9Gt(RHA056)Byg
(B6.129P2-Ranbp9Gt(RHA056)Byg)
|
abnormal male germ cell morphology
|
J:173615
|
abnormal male meiosis
|
J:173615
|
abnormal spermatocyte morphology
|
J:173615
|
abnormal spermatogonia proliferation
|
J:173615
|
arrest of male meiosis
|
J:173615
|
azoospermia
|
J:173615
|
decreased male germ cell number
|
J:173615
|
decreased oocyte number
|
J:173615
|
decreased spermatid number
|
J:173615
|
decreased spermatogonia number
|
J:173615
|
increased male germ cell apoptosis
|
J:173615
|
Ranbp9tm1.1Wyan/Ranbp9tm1.1Wyan
(Not Specified)
|
azoospermia
|
J:222184
|
decreased male germ cell number
|
J:222184
|
increased male germ cell apoptosis
|
J:222184
|
Ranbp9tm1Wyan/Ranbp9tm1Wyan Tg(Stra8-icre)1Reb/0
(involves: C57BL/6J * FVB/NJ)
|
abnormal sperm flagellum morphology
|
J:222184
|
abnormal sperm head morphology
|
J:222184
|
asthenozoospermia
|
J:222184
|
coiled sperm flagellum
|
J:222184
|
decreased male germ cell number
|
J:222184
|
decreased sperm progressive motility
|
J:222184
|
increased male germ cell apoptosis
|
J:222184
|
oligozoospermia
|
J:222184
|
Ranbp10Gt(RRZ226)Byg/Ranbp10Gt(RRZ226)Byg
(either: (involves: 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6))
|
abnormal megakaryocyte differentiation
|
J:193236
|
Rangrftm1.1Tke/Rangrftm1.1Tke
(involves: C57BL/6)
|
abnormal fibroblast physiology
|
J:325055
|
abnormal mitochondrial biogenesis
|
J:325055
|
abnormal mitochondrial physiology
|
J:325055
|
disorganized mitochondrial cristae
|
J:325055
|
increased fibroblast proliferation
|
J:325055
|
increased mitochondrial number
|
J:325055
|
increased mitochondrial size
|
J:325055
|
Rap1atm1Laaq/Rap1atm1Laaq
(either: B6.Cg-Rap1atm1Laaq or (involves: C57BL/6))
|
abnormal leukocyte migration
|
J:140471
|
Rap1atm1Tze/Rap1atm1Tze
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal leukocyte adhesion
|
J:144145
|
decreased T cell proliferation
|
J:144145
|
Rap1gds1tm1Ytk/Rap1gds1tm1Ytk
(involves: 129X1/SvJ * C57BL/6 * DBA)
|
increased cardiomyocyte apoptosis
|
J:62244
|
increased spinal cord apoptosis
|
J:62244
|
increased thymocyte apoptosis
|
J:62244
|
Rapgef1Gt(pGT1.8geo)5Pgr/Rapgef1Gt(pGT1.8geo)5Pgr
(involves: 129/Sv * C57BL/6 * Swiss)
|
abnormal cell adhesion
|
J:80219
|
decreased fibroblast cell migration
|
J:80219
|
Rapgef2tm1.2Hous/Rapgef2tm1.2Hous
(involves: 129S1/Sv)
|
abnormal cell adhesion
|
J:165879
|
abnormal cell migration
|
J:165879
|
decreased cell proliferation
|
J:165879
|
Rapgef3tm1Utak/Rapgef3tm1Utak
(involves: C57BL/6 * CBA)
|
decreased neuron apoptosis
|
J:170436
|
Rapgef6tm1.1Tkat/Rapgef6tm1.1Tkat
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell adhesion
|
J:126164
|
Rapgef6tm1.1Tkat/Rapgef6tm1.1Tkat
(involves: 129P2/OlaHsd)
|
abnormal sperm head morphology
|
J:218581
|
asthenozoospermia
|
J:218581
|
oligozoospermia
|
J:218581
|
Raph1tm1.1Makr/Raph1tm1.1Makr
(involves: C57BL/6NTac)
|
impaired fibroblast cell migration
|
J:208191
|
Rapop1BALB/cHeA/?
(involves: BALB/cHeA * STS/A)
|
abnormal apoptosis
|
J:47265
|
Rapop1BALB/cHeA/? Rapop2STS/A/?
(involves: BALB/cHeA * STS/A)
|
abnormal apoptosis
|
J:47265
|
Rapop2BALB/cHeA/?
(involves: BALB/cHeA * STS/A)
|
abnormal apoptosis
|
J:47265,
J:30582
|
Rapop2STS/A/?
(involves: BALB/cHeA * STS/A)
|
abnormal apoptosis
|
J:47265,
J:30582
|
Rapop3BALB/cHeA/?
(involves: BALB/cHeA * STS/A)
|
abnormal apoptosis
|
J:30582
|
Rapop4C3H/Kam/Rapop4C3H/Kam
(involves: C3H/Kam * C57BL/6J)
|
abnormal apoptosis
|
J:44257
|
Rapop4C3H/Kam/Rapop4C57BL/6J
(involves: C3H/Kam * C57BL/6J)
|
abnormal apoptosis
|
J:44257
|
Rapop7C57BL/6J/Rapop7C3H/Kam
(involves: C3H/Kam * C57BL/6J)
|
abnormal apoptosis
|
J:44257
|
Raratm1Ipc/Raratm1Ipc
(involves: 129S2/SvPas)
|
oligozoospermia
|
J:13574
|
Raratm1Ipc/Raratm1Ipc
(involves: 129S2/SvPas * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:98529
|
abnormal spermatid morphology
|
J:98529
|
oligozoospermia
|
J:98529
|
teratozoospermia
|
J:98529
|
Raratm3.1Ipc/Rara+ Trim24tm1.1Los/Trim24tm1.1Los
(involves: 129/Sv * C57BL/6 * SJL)
|
increased hepatocyte proliferation
|
J:130210
|
Raratm3Ipc/Rara+ Speer6-ps1Tg(Alb-cre)21Mgn/? Trim24tm1Los/Trim24tm1Los
(involves: 129/Sv * C57BL/6 * DBA * SJL)
|
increased hepatocyte proliferation
|
J:130210
|
Raratm3Ipc/Raratm3Ipc Speer6-ps1Tg(Alb-cre)21Mgn/? Trim24tm1Los/Trim24tm1Los
(involves: 129/Sv * C57BL/6 * DBA * SJL)
|
increased hepatocyte proliferation
|
J:130210
|
Rarbtm2Ipc/Rarbtm2Ipc Rargtm3Ipc/Rargtm3Ipc H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129/Sv * C57BL/6 * SJL)
|
decreased periocular mesenchyme apoptosis
|
J:102847
|
Rarres1tm1.2Mhl/Rarres1tm1.2Mhl
(involves: 129S1/SvImJ * C57BL/6 * FVB/N * NIH Black Swiss)
|
abnormal cell physiology
|
J:324270
|
decreased B cell apoptosis
|
J:324270
|
increased B cell proliferation
|
J:324270
|
Rarres2tm1Yktk/Rarres2tm1Yktk
(B6.Cg-Rarres2tm1Yktk)
|
increased muscle cell glucose uptake
|
J:206120
|
Rasa1tm1Paw/Rasa1tm1Paw
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
abnormal cell death
|
J:29825
|
Rasa1tm1Wid/Rasa1tm1Wid
(involves: 129S/SvEv * 129S6/SvEvTac * C57BL/6N)
|
increased cardiomyocyte apoptosis
|
J:189241
|
increased cellular sensitivity to ultraviolet irradiation
|
J:189241
|
increased enterocyte apoptosis
|
J:189241
|
increased sensitivity to induced cell death
|
J:189241
|
Rasa3scat/Rasa3+
(involves: BALB/cBy)
|
maternal effect
|
J:14198
|
Rasa3scat/Rasa3scat
(involves: BALB/cBy)
|
abnormal megakaryocyte differentiation
|
J:186485
|
maternal effect
|
J:14198
|
Rasa3scat/Rasa3scat
(involves: BALB/cBy * BALB/cByJ)
|
abnormal cell cycle checkpoint function
|
J:281271
|
decreased apoptosis
|
J:281271
|
oxidative stress
|
J:281271
|
Rasa4tm1Ywh/Rasa4tm1Ywh
(B6.129S6-Rasa4tm1Ywh)
|
impaired macrophage phagocytosis
|
J:100455
|
Rasd1tm1.1Snyd/Rasd1tm1.1Snyd
(involves: C57BL/6)
|
decreased susceptibility to neuronal excitotoxicity
|
J:195135
|
Rasgrf1enu1H/Rasgrf1+
(involves: BALB/c * C3H/HeN)
|
maternal imprinting
|
J:84625
|
Rasgrf1enu1H/Rasgrf1+
(involves: BALB/c * C3H/HeN * C57BL/6JOlaHsd)
|
maternal imprinting
|
J:84625
|
Rasgrf1enu2H/Rasgrf1+
(involves: BALB/c * C3H/HeN * C57BL/6JOlaHsd)
|
maternal imprinting
|
J:84625
|
Rasgrf1enu2H/Rasgrf1+
(involves: BALB/c * C3H/HeN)
|
maternal imprinting
|
J:84625
|
Rasgrf1tm1Pds/Rasgrf1+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal imprinting
|
J:75397
|
Rasgrf1tm1Toc/Rasgrf1+
(involves: 129)
|
maternal imprinting
|
J:47681
|
Rasgrf1tm2Pds/Rasgrf1+
(involves: 129S4/SvJae)
|
abnormal DNA methylation
|
J:103751
|
abnormal imprinting
|
J:103751
|
Rasgrf1tm3.1Pds/Rasgrf1+
(involves: FVB/N)
|
abnormal imprinting
|
J:85825
|
paternal imprinting
|
J:85825
|
Rasgrf1tm4.1Pds/Rasgrf1+ Tg(Nes-cre)1Kln/0
(involves: 129S4/SvJaeSor * C57BL/6 * SJL)
|
cellular phenotype
|
J:117666
|
Rasgrf1tm4.1Pds/Rasgrf1+ Tg(Zp3-cre)3Mrt/0
(involves: 129S4/SvJaeSor * C57BL/6 * FVB/N)
|
abnormal cell physiology
|
J:117666
|
abnormal imprinting
|
J:117666
|
Rasgrf2tm1Esn/Rasgrf2tm1Esn Vav1tm1Tyb/Vav1tm1Tyb
(involves: 129S1/Sv * 129S2/SvPas * C57BL/10 * C57BR/cd)
|
decreased T cell proliferation
|
J:128985
|
Rasgrp1lag/Rasgrp1lag
(involves: 129 * C57BL/6)
|
decreased T cell proliferation
|
J:85189
|
Rasgrp1tm1.1Wz/Rasgrp1tm1.1Wz
(B6.Cg-Rasgrp1tm1.1Wz)
|
decreased T cell proliferation
|
J:225109
|
Rasgrp4tm1a(KOMP)Lste/Rasgrp4tm1a(KOMP)Lste
(involves: C57BL/6)
|
impaired neutrophil chemotaxis
|
J:186412
|
Rasgrp4tm1d(KOMP)Lste/Rasgrp4tm1d(KOMP)Lste
(involves: 129S4/SvJaeSor * BALB/cJ * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:186412
|
Rasip1tm1.1Oncl/Rasip1tm1.1Oncl
(involves: C57BL/6 * CBA)
|
abnormal vascular endothelial cell differentiation
|
J:174152
|
Rasl10btm1Eno/Rasl10btm1Eno
(involves: 129S/SvEv * C57BL/6)
|
abnormal cell morphology
|
J:187574
|
abnormal vesicle-mediated transport
|
J:187574
|
Rassf1tm1.2Brd/Rassf1tm1.2Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:101369
|
Rassf2tm1Dlim/Rassf2tm1Dlim
(B6.Cg-Rassf2tm1Dlim)
|
abnormal osteoblast differentiation
|
J:181952
|
abnormal osteoclast differentiation
|
J:181952
|
Rassf5tm1Kina/Rassf5tm1Kina
(involves: C57BL/6 * CBA * ICR)
|
abnormal leukocyte migration
|
J:92670
|
Rassf5tm1Kina/Rassf5tm1Kina
(B6.Cg-Rassf5tm1Kina)
|
increased B cell proliferation
|
J:168749
|
increased T cell proliferation
|
J:168749
|
Rassf5tm1Sblee/Rassf5tm1Sblee
(involves: 129S6/SvEvTac * C57BL/6J)
|
decreased fibroblast apoptosis
|
J:166871
|
Rassf9Tg(PDLIM7*)2Cml/Rassf9Tg(PDLIM7*)2Cml
(involves: ICR)
|
abnormal keratinocyte differentiation
|
J:171677
|
increased keratinocyte proliferation
|
J:171677
|
Raver1tm1Hha/Raver1tm1Hha
(B6.129S2-Raver1tm1Hha)
|
cellular phenotype
|
J:137591
|
Raxtm1Mjam/Raxtm1Mjam
(Not Specified)
|
abnormal anterior visceral endoderm cell migration
|
J:40830
|
Rb1tm1.1Jyjw/Rb1+
(either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac))
|
decreased apoptosis
|
J:80087
|
decreased retina apoptosis
|
J:80087
|
Rb1tm1.1Jyjw/Rb1tm1.1Jyjw
(either: (involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6) or (involves: 129S4/SvJae * 129S6/SvEvTac))
|
abnormal retina apoptosis
|
J:80087
|
decreased apoptosis
|
J:80087
|
Rb1tm1.1Jyjw/Rb1tm1.1Jyjw Trp53tm1Tyj/Trp53tm1Tyj
(129S6.129-Trp53tm1Tyj Rb1tm1.1Jyjw)
|
decreased apoptosis
|
J:102483
|
Rb1tm1Brd/Rb1+ Rr70tm1Alb/Rr70+
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal DNA methylation
|
J:113402
|
abnormal imprinting
|
J:113402
|
Rb1tm1Brd/Rb1tm1Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell proliferation
|
J:2516
|
increased neuron apoptosis
|
J:2516
|
Rb1tm1Dwg/Rb1tm1Dwg
(involves: 129/Sv * C57BL/6)
|
abnormal cell cycle
|
J:105548
|
abnormal cell cycle checkpoint function
|
J:105548
|
increased fibroblast proliferation
|
J:105548
|
increased lens fiber apoptosis
|
J:105548
|
Rb1tm1Fad/Rb1+ Tg(KRT14-HPV16E7)2304Plam/0
(involves: 129 * C57BL/6 * FVB)
|
cellular phenotype
|
J:101623
|
Rb1tm1Fad/Rb1tm1Fad
(involves: 129 * C57BL/6)
|
abnormal chromosome morphology
|
J:108366
|
abnormal mitosis
|
J:108366
|
aneuploidy
|
J:108366
|
Rb1tm1Fad/Rb1tm1Fad Tg(KRT14-HPV16E7)2304Plam/0
(involves: 129 * C57BL/6 * FVB)
|
cellular phenotype
|
J:101623
|
Rb1tm1Jyjw/Rb1+
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6))
|
abnormal retina apoptosis
|
J:80087
|
decreased apoptosis
|
J:80087
|
Rb1tm1Jyjw/Rb1tm1Jyjw
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6))
|
decreased apoptosis
|
J:80087
|
decreased retina apoptosis
|
J:80087
|
Rb1tm1Mlh/Rb1tm1Mlh
(either: 129P2/OlaHsd-Rb1tm1Mlh or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB/N))
|
increased apoptosis
|
J:2498
|
Rb1tm1Tyj/Rb1tm1Tyj
(involves: 129S2/SvPas)
|
abnormal cell cycle
|
J:105548
|
abnormal cell cycle checkpoint function
|
J:105548
|
abnormal macrophage differentiation
|
J:105548
|
abnormal neuron differentiation
|
J:81643
|
increased fibroblast proliferation
|
J:105548
|
increased lens fiber apoptosis
|
J:105548
|
increased neuron apoptosis
|
J:81643
|
Rb1tm1Tyj/Rb1tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
increased apoptosis
|
J:37145
|
increased cell proliferation
|
J:81082
|
increased neuron apoptosis
|
J:2511
|
Rb1tm1Tyj/Rb1tm1Tyj
(involves: 129S2/SvPas * 129S6/SvEvTac * FVB/N)
|
abnormal cell differentiation
|
J:175625
|
Rb1tm1Tyj/Rb1tm1Tyj Rbl1tm1Tyj/Rbl1tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
increased apoptosis
|
J:34058
|
Rb1tm1Tyj/Rb1tm1Tyj Tg(Rb1)1Blg/0
(involves: 129S2/SvPas * C57BL/6)
|
increased apoptosis
|
J:37145,
J:98518
|
increased mitotic index
|
J:98518
|
polyploidy
|
J:98518
|
Rb1tm1Tyj/Rb1tm1Tyj Tg(Rb1)1Blg/0
(involves: 129S2/SvPas)
|
abnormal cell cycle
|
J:65679
|
polyploidy
|
J:65679
|
Rb1tm1Tyj/Rb1tm1Tyj Tg(Rb1)1Blg/0 Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas)
|
abnormal cell cycle
|
J:65679
|
abnormal retina apoptosis
|
J:65679
|
polyploidy
|
J:65679
|
Rb1tm1Tyj/Rb1tm1Tyj Trim27Gt(XP0484)Wtsi/Trim27Gt(XP0484)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cell proliferation
|
J:189317
|
Rb1tm1Tyj/Rb1tm2Brn Rbl1tm1Tyj/Rbl1tm1Tyj Trp53tm1Brn/Trp53tm1Tyj Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6 * SJL)
|
abnormal cell proliferation
|
J:120315
|
Rb1tm2.1Fad/Rb1tm2.1Fad
(involves: 129 * C57BL/6)
|
cellular phenotype
|
J:215358
|
Rb1tm2Brn/Rb1tm2Brn Rbl1tm1Htr/Rbl1+ Tg(En2-cre)22Alj/0
(involves: 129P2/OlaHsd * CD-1)
|
abnormal neuronal precursor proliferation
|
J:83783
|
increased neuron apoptosis
|
J:83783
|
Rb1tm2Brn/Rb1tm2Brn Rbl1tm1Htr/Rbl1+ Trp53tm1Brn/Trp53tm1Brn Tg(En2-cre)22Alj/0
(involves: 129P2/OlaHsd * CD-1)
|
cellular phenotype
|
J:83783
|
Rb1tm2Brn/Rb1tm2Brn Rbl1tm1Htr/Rbl1tm1Htr Tg(En2-cre)22Alj/0
(involves: 129P2/OlaHsd * CD-1)
|
abnormal neuronal precursor proliferation
|
J:83783
|
Rb1tm2Brn/Rb1tm2Brn Tg(Col1a1-cre)1Bek/0
(involves: 129 * CD-1)
|
abnormal organ of Corti supporting cell proliferation
|
J:96345
|
Rb1tm2Brn/Rb1tm2Brn Tg(Cyp1a1-cre)1Dwi/0
(involves: 129 * C57BL/6 * CBA)
|
abnormal enterocyte proliferation
|
J:215358
|
Rb1tm2Brn/Rb1tm2Brn Tg(En2-cre)22Alj/0
(involves: 129P2/OlaHsd * CD-1)
|
abnormal neuronal precursor proliferation
|
J:83783
|
increased neuron apoptosis
|
J:83783
|
Rb1tm2Brn/Rb1tm2Brn Tg(Pou4f3-cre)1Devet/0
(involves: 129 * 129S/SvEv)
|
abnormal organ of Corti supporting cell proliferation
|
J:109453
|
Rb1tm2Brn/Rb1tm2Brn Trp53tm1Brn/Trp53tm1Brn Tg(MMTV-cre)105Ayn/0
(FVB.Cg-Trp53tm1Brn Rb1tm2Brn Tg(MMTV-cre)105Ayn)
|
chromosomal instability
|
J:165292
|
Rb1tm2Mlh/Rb1tm2Mlh
(either: 129P2/OlaHsd-Rb1tm2Mlh or (involves: 129P2/OlaHsd * BALB/c) or (involves: 129P2/OlaHsd * FVB/N))
|
increased apoptosis
|
J:2498
|
Rb1tm3Tyj/Rb1tm3.1Tyj Tg(Nes-cre)1Atp/0
(involves: 129S4/SvJae * FVB/N)
|
abnormal neuron differentiation
|
J:81643
|
increased neuron apoptosis
|
J:81643
|
Rb1tm3Tyj/Rb1tm3Tyj
(involves: 129S4/SvJae)
|
polyploidy
|
J:172430
|
Rb1tm3Tyj/Rb1tm3Tyj Rbl1tm1Tyj/Rbl1tm1Tyj Tg(Nes-cre)1Atp/0
(involves: 129S2/SvPas * 129S4/SvJae * FVB/N)
|
abnormal retina apoptosis
|
J:91406
|
Rb1tm3Tyj/Rb1tm3Tyj Rbl2tm1Tyj/Rbl2tm1Tyj Tg(Nes-cre)1Atp/0
(involves: 129S2/SvPas * 129S4/SvJae * FVB/N)
|
abnormal retina apoptosis
|
J:91406
|
Rb1tm3Tyj/Rb1tm3Tyj Rbl2tm2.1Tyj/Rbl2tm2.1Tyj Tg(Pax6-cre,GFP)2Pgr/0
(involves: 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB/N)
|
increased retina apoptosis
|
J:119919
|
Rb1tm3Tyj/Rb1tm3Tyj Tg(Nes-cre)1Atp/0
(involves: 129S4/SvJae * FVB/N)
|
increased retina apoptosis
|
J:91406
|
Rb1tm3Tyj/Rb1tm3Tyj Tg(Pax6-cre,GFP)2Pgr/0
(involves: 129S4/SvJae * 129X1/SvJ * C57BL/6 * FVB/N)
|
increased retina apoptosis
|
J:119919
|
Rb1tm3Tyj/Rb1tm3Tyj Tg(Pax6-cre,GFP)2Pgr/0
(involves: 129S4/SvJae)
|
increased retina apoptosis
|
J:91406
|
Rb1tm3Tyj/Rb1tm3Tyj Tg(tetO-MYC)36aBop/0 Tg(Cebpb-tTA)5Bjd/0
(involves: FVB/N * NMRI)
|
polyploidy
|
J:172430
|
Rb1tm3Tyj/Rb1tm3Tyj Trp53tm1Tyj/Trp53tm1Tyj Tg(Nes-cre)1Atp/0
(involves: 129S2/SvPas * 129S4/SvJae * FVB/N)
|
increased retina apoptosis
|
J:91406
|
Rb1cc1tm1.1Guan/Rb1cc1tm1.1Guan Tg(BEST1-cre)1Jdun/0
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired autophagy
|
J:282249
|
Rb1cc1tm1.1Guan/Rb1cc1tm1.1Guan Tg(Tek-cre)12Flv/0
(B6.Cg-Rb1cc1tm1.1Guan Tg(Tek-cre)12Flv)
|
abnormal autophagy
|
J:167258
|
abnormal mitochondrial morphology
|
J:167258
|
increased hematopoietic stem cell proliferation
|
J:167258
|
Rb1cc1tm1.2Guan/Rb1cc1tm1.2Guan
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cell mass
|
J:114498
|
increased fibroblast apoptosis
|
J:114498
|
increased hepatocyte apoptosis
|
J:114498
|
Rb(12.Ts171665Dn)2Cje/0
(involves: C3H/HeSnJ * C57BL/6JEiJ)
|
increased neuron apoptosis
|
J:110478
|
Rbbp4em1(IMPC)Mbp/Rbbp4em1(IMPC)Mbp
(C57BL/6NCrl-Rbbp4em1(IMPC)Mbp/Mmucd)
|
abnormal cell physiology
|
J:290528
|
cellular phenotype
|
J:290528
|
increased embryonic tissue cell apoptosis
|
J:290528
|
Rbbp6tm1Xya/Rbbp6tm1Xya
(involves: 129S6/SvEvTac)
|
increased apoptosis
|
J:121586
|
Rbbp8tm1Whl/Rbbp8tm1Whl
(Not Specified)
|
abnormal cell cycle
|
J:97648
|
Rbbp8tm2.1Thl/Rbbp8tm2.1Thl
(involves: 129)
|
cellular phenotype
|
J:197743
|
Rbck1tm1Kiwa/Rbck1tm1Kiwa
(B6.Cg-Rbck1tm1Kiwa)
|
increased hepatocyte apoptosis
|
J:158069
|
Rbfox2tm1.1Dblk/Rbfox2tm1.1Dblk E2f1Tg(Wnt1-cre)2Sor/E2f1+ Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
(involves: 129S/Sv * 129X1/SvJ * C57BL/6J)
|
cellular phenotype
|
J:279139
|
Rbfox2tm1.1Dblk/Rbfox2tm1.1Dblk Pax3tm1(cre)Joe/0 Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J)
|
cellular phenotype
|
J:279139
|
Rbfox2tm1.1Dblk/Rbfox2tm1.1Dblk Tg(Nes-cre)1Kln/0
(involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL)
|
abnormal Purkinje cell migration
|
J:181631
|
decreased cerebellar granule cell precursor proliferation
|
J:181631
|
increased neuron apoptosis
|
J:181631
|
Rbfox3tm1a(EUCOMM)Hmgu/Rbfox3tm1a(EUCOMM)Hmgu
(B6Dnk;B6N-Rbfox3tm1a(EUCOMM)Hmgu/H)
|
abnormal neuron differentiation
|
J:240501
|
decreased neuronal precursor proliferation
|
J:240501
|
Rbl1tm1.1Fad/Rbl1tm1.1Fad
(involves: 129 * FVB/N)
|
cellular phenotype
|
J:217445
|
Rbl1tm1.1Fad/Rbl1tm1.1Fad Rbl2tm1Tyj/Rbl2tm1Tyj
(involves: 129S2/SvPas * C57BL/6 * FVB/N)
|
cellular phenotype
|
J:217445
|
Rbl1tm1Mru/Rbl1tm1Mru
(involves: 129S4/SvJae * BALB/cJ)
|
increased cell proliferation
|
J:51060
|
increased fibroblast proliferation
|
J:51060
|
Rbl1tm1Mru/Rbl1tm1Mru
(involves: 129S4/SvJae * BALB/c * C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:92520
|
Rbl1tm1Tyj/Rbl1tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
cellular phenotype
|
J:34058
|
Rbl1tm1Tyj/Rbl1tm1Tyj Rbl2tm1Tyj/Rbl2tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
abnormal keratinocyte differentiation
|
J:82802
|
Rbl1tm3.1Jsag/Rbl1tm3.1Jsag
(involves: C57BL/6)
|
increased fibroblast proliferation
|
J:161509
|
Rbl2tm1Mru/Rbl2tm1Mru
(involves: 129S4/SvJae * BALB/cJ)
|
abnormal cell proliferation
|
J:50516
|
abnormal neuron differentiation
|
J:50516
|
cellular phenotype
|
J:50516
|
increased apoptosis
|
J:50516
|
increased neuron apoptosis
|
J:50516
|
Rbl2tm1Tyj/Rbl2tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
cellular phenotype
|
J:34725
|
Rbm3tm1Ttg/Rbm3tm1Ttg
(involves: 129P2/OlaHsd)
|
abnormal cell cycle
|
J:174947
|
decreased fibroblast proliferation
|
J:174947
|
Rbm5sda/Rbm5sda
(C57BL/6-Rbm5sda/MarpApb)
|
abnormal male germ cell apoptosis
|
J:104190
|
abnormal spermatid morphology
|
J:104190
|
azoospermia
|
J:104190
|
Rbm5sda/Rbm5sda
(involves: C57BL/6J * CBA)
|
azoospermia
|
J:223049
|
increased male germ cell apoptosis
|
J:223049
|
Rbm14em1Wli/Rbm14em1Wli
(involves: ICR)
|
abnormal cell cycle
|
J:290444
|
increased apoptosis
|
J:290444
|
Rbm15tm1Swm/Rbm15tm1Swm Tg(Mx1-cre)1Cgn/0
(involves: 129X1/SvJ * C57BL/6 * CBA)
|
abnormal megakaryocyte differentiation
|
J:152262
|
Rbm19Gt(XC768)Byg/Rbm19Gt(XC768)Byg
(involves: 129P2/OlaHsd)
|
abnormal cell nucleus morphology
|
J:145174
|
Rbm24tm1.1Xch/Rbm24tm1.1Xch
(involves: FVB/N)
|
increased embryonic tissue cell apoptosis
|
J:259290
|
Rbm46em1Rpc/Rbm46em1Rpc
(involves: C57BL/6J * SJL/J)
|
absent oocytes
|
J:330079
|
Rbm47Gt(D027B04)Wrst/Rbm47Gt(D027B04)Wrst
(involves: 129S2/SvPas)
|
abnormal cell physiology
|
J:217130
|
Rbmxl2tm1.2Dell/Rbmxl2tm1.2Dell
(involves: 129 * BALB/c * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:275203
|
arrest of male meiosis
|
J:275203
|
azoospermia
|
J:275203
|
decreased elongated spermatid number
|
J:275203
|
decreased round spermatid number
|
J:275203
|
decreased spermatid number
|
J:275203
|
increased male germ cell apoptosis
|
J:275203
|
Rbp2tm1Eli/Rbp2tm1Eli
(B6.129-Rbp2tm1Eli)
|
maternal effect
|
J:79282
|
Rbp4tm1.1Mma/Rbp4tm1.1Mma
(involves: 129 * C57BL/6J)
|
abnormal spermatid morphology
|
J:108574
|
Rbp4tm1Gott/Rbp4tm1Gott
(involves: 129/Sv * C57BL/6 * CD-1)
|
abnormal fetal cardiomyocyte proliferation
|
J:82903
|
Rbpjtm1Hon/Rbpjtm1.1Hon Tg(Pax7-cre/ERT2)1Cbm/0
(involves: 129P2/OlaHsd * BALB/cJ)
|
abnormal neuron differentiation
|
J:130251
|
Rbpjtm1Hon/Rbpjtm1Hon Tg(Cyp1a1-cre)1Dwi/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal intestinal goblet cell morphology
|
J:99348
|
Rbpjtm1Hon/Rbpjtm1Hon Tg(Lck-cre)19Hhan/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA)
|
increased T cell proliferation
|
J:168475
|
Rbpjtm1Hon/Rbpjtm1Hon Tg(Nes-cre)1Wme/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal cell differentiation
|
J:82337
|
Rbpjtm1Kyo/Rbpjtm1Hon Tg(Tek-cre)12Flv/0
(involves: 129P2/OlaHsd * C3H * C57BL/6)
|
abnormal vascular regression
|
J:93125
|
Rbpjtm1Kyo/Rbpjtm1Kyo
(involves: 129S2/SvPas * C57BL/6)
|
abnormal vascular regression
|
J:93125
|
Rbpjtm1Kyo/Rbpjtm1Kyo
(involves: 129S2/SvPas)
|
abnormal fetal cardiomyocyte proliferation
|
J:119151
|
Rbpmsem1Eno/Rbpmsem1Eno
(involves: C3H * C57BL/6)
|
patent ductus arteriosus
|
J:324468
|
Rbx1Gt(XB674)Byg/Rbx1+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle
|
J:147759
|
decreased cell proliferation
|
J:147759
|
Rbx1Gt(XB674)Byg/Rbx1Gt(XB674)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cell proliferation
|
J:147759
|
increased embryonic tissue cell apoptosis
|
J:147759
|
Rc3h1san/Rc3h1san
(involves: C57BL/6JSfdAnu)
|
increased T cell proliferation
|
J:199407
|
Rc3h1tm1.1Mass/Rc3h1tm1.1Mass Rc3h2tm1c(KOMP)Wtsi/Rc3h2tm1c(KOMP)Wtsi Tg(Cd4-cre)1Cwi/?
(involves: C57BL/6N * DBA/2)
|
increased T cell proliferation
|
J:196136
|
Rcan1tm1Emar/Rcan1tm1Emar
(involves: 129P2/OlaHsd * C57BL/6)
|
oxidative stress
|
J:132745
|
Rcan1tm1Fmc/Rcan1tm1Fmc
(involves: 129S4/SvJae)
|
abnormal T cell apoptosis
|
J:85148
|
decreased T cell proliferation
|
J:85148
|
Rcan1tm1Jmol/Rcan1tm1Jmol Rcan2tm1Jmol/Rcan2tm1Jmol
(involves: 129 * C57BL/6)
|
decreased T cell proliferation
|
J:109586
|
Rcan1tm1Jmol/Rcan1tm1Jmol Rcan2tm1Jmol/Rcan2tm1Jmol Ppp3cbtm1Jmk/Ppp3cbtm1Jmk
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased T cell proliferation
|
J:109586
|
Rchy1tm1.1Raz/Rchy1tm1.1Raz
(involves: 129 * C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:175870
|
Rcor2tm1c(EUCOMM)Wtsi/Rcor2tm1c(EUCOMM)Wtsi Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6N * SJL)
|
abnormal cell cycle
|
J:235702
|
decreased neuronal precursor proliferation
|
J:235702
|
Rdh10tm1c(KOMP)Wtsi/Rdh10tm1c(KOMP)Wtsi Tg(Amh-cre)8815Reb/0 Tg(Stra8-icre)1Reb/0
(involves: C57BL/6 * C57BL/6N * FVB/N * SJL)
|
abnormal spermatogonia morphology
|
J:193281
|
arrest of male meiosis
|
J:193281
|
Rdh12tm1Kpal/Rdh12tm1Kpal
(involves: 129S/SvEv * C57BL/6J)
|
abnormal retina apoptosis
|
J:117483
|
Rec8mei8/Rec8mei8
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal chromosomal synapsis
|
J:209347
|
abnormal male meiosis
|
J:209347,
J:94208
|
abnormal synaptonemal complex
|
J:209347
|
arrest of male meiosis
|
J:209347,
J:94208
|
Rec8mei8/Rec8mei8
(B6.Cg-Rec8mei8)
|
abnormal male meiosis
|
J:205574
|
Rec8mei8/Rec8mei8 Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129S4/SvJae * 129X1/SvJ * C57BL/6J)
|
abnormal male meiosis
|
J:209347
|
abnormal synaptonemal complex
|
J:209347
|
Rec8tm1.1Kktk/Rec8tm1.1Kktk
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal female meiosis
|
J:166151
|
Rec8tm1b(KOMP)Wtsi/Rec8tm1b(KOMP)Wtsi
(B6N(Cg)-Rec8tm1b(KOMP)Wtsi)
|
abnormal double-strand DNA break repair
|
J:280261
|
abnormal male meiosis
|
J:280261
|
Rec8tm1b(KOMP)Wtsi/Rec8tm1b(KOMP)Wtsi Stag3tm1e.1(KOMP)Wtsi/Stag3tm1e.1(KOMP)Wtsi
(B6N(Cg)-Rec8tm1b(KOMP)Wtsi Stag3tm1e.1(KOMP)Wtsi)
|
abnormal double-strand DNA break repair
|
J:280261
|
abnormal male meiosis
|
J:280261
|
abnormal synaptonemal complex
|
J:280261
|
Rec8tm1Mjm/Rec8tm1Mjm
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * C57BL/6))
|
abnormal female meiosis
|
J:99402
|
absent oocytes
|
J:99402
|
arrest of male meiosis
|
J:99402
|
azoospermia
|
J:99402
|
Rec114tm1(KOMP)Wtsi/Rec114tm1(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal chromosomal synapsis
|
J:271216
|
abnormal double-strand DNA break repair
|
J:271216
|
abnormal female meiosis
|
J:271216
|
abnormal male meiosis
|
J:271216
|
abnormal meiosis
|
J:271216
|
abnormal oogenesis
|
J:271216
|
abnormal spermatocyte morphology
|
J:276412
|
abnormal synaptonemal complex
|
J:271216
|
decreased male germ cell number
|
J:271216
|
Rec114tm1.2(KOMP)Wtsi/Rec114tm1.2(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal chromosomal synapsis
|
J:271216
|
abnormal meiosis
|
J:271216
|
abnormal oogenesis
|
J:271216
|
abnormal synaptonemal complex
|
J:271216
|
Recktm1Ito/Recktm1Ito
(either: (involves: 129/Sv * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6J))
|
abnormal basal lamina morphology
|
J:107674
|
Recql4tm1Furu/Recql4tm1Furu
(Not Specified)
|
decreased inner cell mass proliferation
|
J:85891
|
Recql4tm1Glu/Recql4tm1Glu
(involves: 129S7/SvEvBrd * C57BL/6J)
|
chromosome breakage
|
J:97101
|
Recql5tm1.1Glu/Recql5tm1.1Glu
(involves: 129S7/SvEvBrd * C57BL/6)
|
elevated level of mitotic sister chromatid exchange
|
J:97667
|
Recqltm1Pjb/Recqltm1Pjb
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal chromosome morphology
|
J:118989
|
aneuploidy
|
J:118989
|
decreased fibroblast proliferation
|
J:118989
|
elevated level of mitotic sister chromatid exchange
|
J:118989
|
spontaneous chromosome breakage
|
J:118989
|
Reep1Gt(OST398247)Tigm/Reep1Gt(OST398247)Tigm
(B6J.Cg-Reep1Gt(OST398247)Tigm)
|
abnormal endoplasmic reticulum morphology
|
J:239250
|
abnormal fat cell differentiation
|
J:239250
|
Reep6em2Ruch/Reep6em2Ruch
(involves: C57BL/6 * C57BL/6J)
|
asthenozoospermia
|
J:295354
|
increased endoplasmic reticulum stress
|
J:243288
|
oligozoospermia
|
J:295354
|
teratozoospermia
|
J:295354
|
Reg2tm1Lchr/Reg2tm1Lchr
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased hepatocyte proliferation
|
J:140235
|
increased cellular sensitivity to oxidative stress
|
J:140235
|
Reltm1Brv/Reltm1Brv
(involves: 129S1/Sv)
|
impaired macrophage chemotaxis
|
J:46911
|
Reltm1Grd/Rel+
(involves: 129S1/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:28435
|
Reltm1Grd/Reltm1Grd
(involves: 129S1/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:28435
|
decreased T cell proliferation
|
J:28435
|
Reltm1Grd/Reltm1Grd Relatm1Bal/Relatm1Bal
(B6.129S-Reltm1Grd Relatm1Bal)
|
abnormal monocyte differentiation
|
J:111325
|
increased hepatocyte apoptosis
|
J:111325
|
Reltm1Grd/Reltm1Grd Relatm1Bal/Relatm1Bal Tnftm1Ljo/Tnftm1Ljo
(involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJae)
|
abnormal cell cycle
|
J:91366
|
decreased cell proliferation
|
J:91366
|
Reltm1Hcl/Rel+
(involves: 129S4/SvJae * C57BL/6)
|
decreased T cell proliferation
|
J:53513
|
Reltm1Hcl/Reltm1Hcl
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:75621
|
decreased apoptosis
|
J:118907
|
decreased B cell proliferation
|
J:75621
|
decreased DNA replication
|
J:75621
|
decreased T cell proliferation
|
J:53513,
J:79107
|
increased neuron apoptosis
|
J:111862
|
Relatm1.2Gho/Relatm1.2Gho
(involves: 129S6/SvEvTac * C57BL/6)
|
increased hepatocyte apoptosis
|
J:134684
|
Relatm1Bal/Relatm1Bal
(involves: 129S4/SvJae * C57BL/6J)
|
increased hepatocyte apoptosis
|
J:28390
|
Relatm1Bal/Relatm1Bal
(involves: 129S4/SvJae)
|
abnormal cell death
|
J:28390
|
increased neuron apoptosis
|
J:119844
|
Relatm1Bal/Relatm1Bal
(B6.129S4-Relatm1Bal)
|
increased hepatocyte apoptosis
|
J:111325
|
Relatm1Bal/Relatm1Bal Tg(SERPINA1-BCL2)1Pva/0
(involves: 129S4/SvJae * C57BL/6 * DBA/2)
|
increased hepatocyte apoptosis
|
J:126292
|
Relatm1Yuo/Relatm1Yuo
(involves: 129S/SvEv)
|
decreased B cell proliferation
|
J:63099
|
decreased T cell proliferation
|
J:63099
|
RelbTg(H2-K1/GH1)106Bri/RelbTg(H2-K1/GH1)106Bri
(C57BL/6-RelbTg(H2-K1/GH1)106Bri)
|
decreased T cell proliferation
|
J:76450
|
Relbtm1Brv/Relbtm1Brv
(involves: 129S2/SvPas * C57BL/6)
|
decreased B cell proliferation
|
J:40630
|
impaired neutrophil phagocytosis
|
J:40630
|
Relbtm1Brv/Relbtm1Brv
(either: (involves: 129S2/SvPas) or (involves: C57BL/6) or (involves: 129S2/SvPas * C57BL/6))
|
abnormal keratinocyte apoptosis
|
J:63950
|
increased keratinocyte proliferation
|
J:63950
|
Relnrl/Relnrl
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal neuron differentiation
|
J:12728
|
Relnrl/Relnrl
(C3.Cg-Relnrl)
|
abnormal neuronal migration
|
J:12728
|
Relnrl/Relnrl Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw
(involves: BALB/c * C57BL/6 * C57BL/6J)
|
abnormal axon extension
|
J:168258
|
Relttm1Hlee/Relttm1Hlee
(Not Specified)
|
increased T cell proliferation
|
J:266480
|
repro2/repro2
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal sperm fibrous sheath morphology
|
J:117563
|
abnormal sperm nucleus morphology
|
J:117563
|
abnormal spermatid morphology
|
J:117563
|
absent sperm head
|
J:117563
|
coiled sperm flagellum
|
J:117563
|
immotile sperm
|
J:117563
|
oligozoospermia
|
J:117563
|
short sperm flagellum
|
J:117563
|
teratozoospermia
|
J:117563
|
repro3/repro3
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:117563
|
abnormal sperm head morphology
|
J:117563
|
abnormal sperm nucleus morphology
|
J:117563
|
abnormal spermatid morphology
|
J:117563
|
absent sperm mitochondrial sheath
|
J:117563
|
immotile sperm
|
J:117563
|
oligozoospermia
|
J:117563
|
short sperm flagellum
|
J:117563
|
teratozoospermia
|
J:117563
|
repro10/repro10
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
repro13/repro13
(involves: C3HeB/FeJ * C57BL/6J)
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
repro14/repro14
(B6;C3Fe-repro14/J)
|
arrest of male meiosis
|
J:92463
|
azoospermia
|
J:92463
|
decreased oocyte number
|
J:92463
|
repro15/repro15
(involves: C3HeB/FeJ * C57BL/6J)
|
globozoospermia
|
J:92463
|
repro16/repro16
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
repro17/repro17
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
short sperm flagellum
|
J:92463
|
repro19/repro19
(B6;C3Fe-repro19/J)
|
abnormal sperm motility
|
J:92463
|
oligozoospermia
|
J:92463
|
teratozoospermia
|
J:92463
|
repro20/repro20
(involves: C3HeB/FeJ * C57BL/6J)
|
absent sperm flagellum
|
J:92463
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
short sperm flagellum
|
J:92463
|
repro21/repro21
(involves: C3HeB/FeJ * C57BL/6J)
|
absent sperm flagellum
|
J:92463
|
decreased elongated spermatid number
|
J:92463
|
globozoospermia
|
J:92463
|
immotile sperm
|
J:92463
|
oligozoospermia
|
J:92463
|
repro24/repro24
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
repro26/repro26
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal spermatid morphology
|
J:92463
|
absent sperm flagellum
|
J:92463
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
repro28/repro28
(involves: C3HeB/FeJ * C57BL/6J)
|
absent sperm flagellum
|
J:92463
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
kinked sperm flagellum
|
J:92463
|
oligozoospermia
|
J:92463
|
repro30/repro30
(involves: C3HeB/FeJ * C57BL/6J)
|
arrest of male meiosis
|
J:92463
|
azoospermia
|
J:92463
|
repro31/repro31
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal male germ cell morphology
|
J:92463
|
abnormal sperm motility
|
J:92463
|
abnormal spermatid morphology
|
J:92463
|
repro33/repro33
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal male germ cell morphology
|
J:92463
|
abnormal sperm motility
|
J:92463
|
repro36/repro36
(B6;C3Fe-repro36/J)
|
arrest of male meiosis
|
J:92463
|
azoospermia
|
J:92463
|
decreased oocyte number
|
J:92463
|
repro46/repro46
(B6;C3Fe-repro46/J)
|
arrest of male meiosis
|
J:92463
|
azoospermia
|
J:92463
|
repro47/repro47
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
teratozoospermia
|
J:92463
|
repro48/repro48
(involves: C3HeB/FeJ * C57BL/6J)
|
oligozoospermia
|
J:92463
|
repro49/repro49
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
globozoospermia
|
J:92463
|
teratozoospermia
|
J:92463
|
repro50/repro50
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal sperm head morphology
|
J:92463
|
immotile sperm
|
J:92463
|
oligozoospermia
|
J:92463
|
short sperm flagellum
|
J:92463
|
teratozoospermia
|
J:92463
|
repro51/repro51
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
teratozoospermia
|
J:92463
|
repro52/repro52
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
repro53/repro53
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
repro54/repro54
(involves: C3HeB/FeJ * C57BL/6J)
|
asthenozoospermia
|
J:92463
|
oligozoospermia
|
J:92463
|
teratozoospermia
|
J:92463
|
Resttm1.1Jhsi/Resttm1.1Jhsi
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:174056
|
Resttm1.1Yasu/Resttm1.2Yasu Alpltm1(cre)Nagy/Alpl+
(involves: 129 * C57BL/6 * C57BL/6J)
|
decreased primordial germ cell number
|
J:190948
|
increased primordial germ cell apoptosis
|
J:190948
|
Resttm1.2Bban/Rest+
(involves: 129S4/SvJaeSor * FVB/N)
|
abnormal kinocilium morphology
|
J:265659
|
Resttm1And/Resttm1And
(involves: 129S7/SvEvBrd * C57BL/6J)
|
increased embryonic tissue cell apoptosis
|
J:50169
|
Resttm1Mlit/Resttm1Mlit Tg(Eno2-cre)#Mlit/0
(involves: 129S1/Sv * C57BL/6 * DBA)
|
increased neuron apoptosis
|
J:173834
|
Resttm1Ymat/Resttm1Ymat
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased primordial germ cell number
|
J:190948
|
increased primordial germ cell apoptosis
|
J:190948
|
Rettm1Cos/Rettm1Cos
(involves: 129S/SvEv * MF1)
|
abnormal enteric neural crest cell migration
|
J:30830
|
increased metanephric mesenchyme apoptosis
|
J:84282
|
Rettm1Giro/Rettm1Giro
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal neuron differentiation
|
J:141658
|
Rettm1Heno/Rettm2(RET)Jmi
(involves: 129X1/SvJ * C57BL/6)
|
abnormal enteric neural crest cell migration
|
J:159854
|
Rettm1Jmi/Rettm1Jmi
(involves: 129X1/SvJ)
|
increased cell proliferation
|
J:71881
|
increased neuron apoptosis
|
J:71881
|
Rettm2(RET)Jmi/Rettm3.1(Bcl2l1)Heno
(involves: 129/Sv * C57BL/6)
|
abnormal enteric neural crest cell migration
|
J:159854
|
Rettm2(RET)Vpa/Rettm2(RET)Vpa
(involves: 129P2/OlaHsd)
|
abnormal enteric neural crest cell migration
|
J:71588
|
Rettm2.1Heno/Rettm2(RET)Jmi
(involves: 129S/Sv * C57BL/6 * FVB/N)
|
abnormal enteric neural crest cell migration
|
J:135153
|
Rettm2.1Heno/Rettm2.1Heno
(involves: 129S/Sv * C57BL/6 * FVB/N)
|
increased neuron apoptosis
|
J:135153
|
Rettm3.1(Bcl2l1)Heno/Ret+
(involves: 129/Sv * C57BL/6)
|
decreased neuron apoptosis
|
J:159854
|
Rettm3Cos/Rettm3Cos
(involves: 129S1/Sv * FVB/N)
|
abnormal enteric neural crest cell migration
|
J:116089
|
Rettm11(RET)Jmi/Rettm11(RET)Jmi
(involves: 129X1/SvJ * 129S1/Sv * C57BL/6)
|
increased kidney apoptosis
|
J:105047
|
Rev3ltm1Kaji/Rev3ltm1Kaji
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased embryonic tissue cell apoptosis
|
J:74111
|
Rev3ltm1Ndew/Rev3ltm1Ndew
(involves: 129P2/OlaHsd * C57BL/6)
|
spontaneous chromosome breakage
|
J:75450
|
Rev3ltm1Rsky/Rev3ltm1.1Rsky Tg(Cr2-cre)3Cgn/?
(involves: C57BL/6)
|
decreased B cell proliferation
|
J:146453
|
spontaneous chromosome breakage
|
J:146453
|
Rev3ltm1Rwd/Rev3ltm1Rwd
(involves: 129P2/OlaHsd)
|
increased cell death
|
J:65201
|
Rflnatm1Tfur/Rflnatm1Tfur Rflnbtm1Sia/Rflnbtm1Sia
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj)
|
cellular phenotype
|
J:210363
|
decreased chondrocyte proliferation
|
J:210363
|
increased chondrocyte apoptosis
|
J:210363
|
Rfwd3tm1.1Dtch/Rfwd3tm1.1Dtch
(involves: C57BL/6)
|
increased cellular sensitivity to DNA damaging agents
|
J:248005
|
oligozoospermia
|
J:248005
|
Rfx2Gt(IST10638H11)Tigm/Rfx2Gt(IST10638H11)Tigm
(either: C57BL/6N-Rfx2Gt(IST10638H11)Tigm or (involves: C57BL/6N * CD-1))
|
abnormal spermatid morphology
|
J:227136
|
multinucleated giant male germ cells
|
J:227136
|
Rfx2tm1.1Wrth/Rfx2tm1.1Wrth
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal acrosome assembly
|
J:228765
|
abnormal acrosome morphology
|
J:228765
|
abnormal Golgi apparatus morphology
|
J:228765
|
abnormal sperm axoneme morphology
|
J:228765
|
cellular phenotype
|
J:228765
|
detached acrosome
|
J:228765
|
ectopic manchette
|
J:228765
|
multinucleated giant male germ cells
|
J:228765
|
Rfx2tm1.2Wrth/Rfx2tm1.2Wrth
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
abnormal acrosome assembly
|
J:228765
|
abnormal acrosome morphology
|
J:228765
|
abnormal Golgi apparatus morphology
|
J:228765
|
abnormal sperm axoneme morphology
|
J:228765
|
cellular phenotype
|
J:228765
|
detached acrosome
|
J:228765
|
ectopic manchette
|
J:228765
|
multinucleated giant male germ cells
|
J:228765
|
Rfx2tm1Hncs/Rfx2tm1Hncs
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal acrosome morphology
|
J:230575
|
abnormal manchette morphology
|
J:230575
|
abnormal sperm axoneme morphology
|
J:230575
|
abnormal spermatid morphology
|
J:230575
|
azoospermia
|
J:230575
|
decreased elongated spermatid number
|
J:230575
|
decreased round spermatid number
|
J:230575
|
increased male germ cell apoptosis
|
J:230575
|
multinucleated giant male germ cells
|
J:230575
|
Rfx3tm1.1Wrth/Rfx3tm1.1Wrth
(involves: 129 * C57BL/6J)
|
abnormal motile primary cilium morphology
|
J:89880
|
Rfx3tm2.1Wrth/Rfx3tm2.1Wrth
(involves: 129 * C57BL/6J)
|
abnormal motile primary cilium morphology
|
J:89880
|
Rfx4m269Asp/Rfx4m269Asp
(involves: C57BL/6J * FVB/NJ)
|
abnormal brain ependyma motile cilium morphology
|
J:186055
|
abnormal spinal cord motile cilium morphology
|
J:186055
|
Rgcctm1Hrus/Rgcctm1Hrus
(involves: 129S6/SvEvTac * C57BL/6)
|
increased T cell proliferation
|
J:279555
|
Rgntm1Aish/Y
(involves: 129P2/OlaHsd)
|
abnormal hepatocyte mitochondrial morphology
|
J:88791
|
increased cellular sensitivity to oxidative stress
|
J:135721
|
oxidative stress
|
J:135721,
J:107922
|
Rgntm1Aish/Rgntm1Aish
(involves: 129P2/OlaHsd * C57BL/6)
|
increased hepatocyte apoptosis
|
J:79342
|
Rgs1tm1Jhk/Rgs1tm1Jhk
(B6.129P2-Rgs1tm1Jhk)
|
enhanced B cell migration
|
J:90780
|
Rgs2tm1Pngr/Rgs2tm1Pngr
(involves: C57BL/6J)
|
abnormal T cell proliferation
|
J:77273
|
Rgs4tm1Sdlk/Rgs4tm1Sdlk Tg(Myh11-icre/ERT2)1Soff/?
(involves: FVB/N)
|
abnormal macrophage chemotaxis
|
J:215588
|
Rgs10tm1Ypl/Rgs10tm1Ypl
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:123167
|
Rgs16tm1Tmw/Rgs16tm1Tmw
(involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6)
|
increased fatty acid oxidation
|
J:172091
|
Rgs18tm1.1Ics/Rgs18tm1.1Ics
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal megakaryocyte differentiation
|
J:225296
|
Rhbdd1tm1.1Mfm/Rhbdd1tm1.1Mfm
(involves: 129S/SvEv * C57BL/6J)
|
abnormal endoplasmic reticulum morphology
|
J:325547
|
increased endoplasmic reticulum stress
|
J:325547
|
Rhbdf2cub/Rhbdf2cub
(MRL.Cg-Rhbdf2cub)
|
abnormal fibroblast physiology
|
J:250259
|
Rhbdf2Uncv/Rhbdf2Uncv
(involves: BALB/c)
|
azoospermia
|
J:52604
|
Rhebtm1.1Yelg/Rheb+ Tsc1tm1Chdl/Tsc1tm1Chdl
(B6.129P2-Tsc1tm1Chdl Rhebtm1.1Yelg)
|
increased embryonic tissue cell apoptosis
|
J:170999
|
Rhebtm1.1Yelg/Rhebtm1.1Yelg
(B6.129P2-Rhebtm1.1Yelg)
|
decreased fibroblast proliferation
|
J:170999
|
increased embryonic tissue cell apoptosis
|
J:170999
|
Rhebtm1Pfw/Rhebtm1Pfw Tg(Amh-cre)8815Reb/0
(involves: 129S1/SvImJ * FVB/N)
|
oligozoospermia
|
J:268375
|
RhoR3/RhoR3
(C57BL/6J-RhoR3)
|
increased retina apoptosis
|
J:153281
|
Rhotm1.1(RHO*)Akgr/Rho+
(involves: 129S7/SvEvBrd * BALB/c * FVB/N)
|
increased retina apoptosis
|
J:203860
|
Rhotm1.1(RHO*)Akgr/Rhotm1.1(RHO*)Akgr
(involves: 129S7/SvEvBrd * BALB/c * FVB/N)
|
increased retina apoptosis
|
J:203860
|
RhoTvrm4/Rho+
(B6.Cg-RhoTvrm4/Pjn)
|
increased retina apoptosis
|
J:159523
|
Rhoatm1.1Tpal/Rhoa+ Tg(Cd4-cre/ERT2)11Gnri/0
(involves: C57BL/6)
|
increased T cell proliferation
|
J:257764
|
Rhoatm1Jrel/Rhoatm1Jrel Tg(Pou3f4-cre)32Cren/0
(involves: CD-1)
|
abnormal neuronal precursor proliferation
|
J:171199
|
increased spinal cord apoptosis
|
J:171199
|
premature neuronal precursor differentiation
|
J:171199
|
Rhoatm1Yuyo/Rhoatm1Yuyo H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: C57BL/6J * CBA/J)
|
abnormal neuron proliferation
|
J:172044
|
Rhobtm1Gcp/Rhobtm1Gcp
(involves: 129)
|
abnormal cell adhesion
|
J:71577
|
abnormal cell physiology
|
J:71577
|
decreased fibroblast cell migration
|
J:71577
|
Rhoctm1Mak/Rhoctm1Mak
(involves: 129P2/OlaHsd)
|
abnormal cell morphology
|
J:100482
|
Rhogtm1Tnr/Rhogtm1Tnr
(involves: 129)
|
increased B cell proliferation
|
J:87580
|
Rhohtm1Brak/Rhohtm1Brak
(involves: 129/Sv * C57BL/6)
|
abnormal T cell proliferation
|
J:143161
|
decreased T cell apoptosis
|
J:143161
|
decreased T cell proliferation
|
J:143161
|
increased T cell proliferation
|
J:143161
|
Rhohtm1Hasu/Rhohtm1Hasu
(B6.Cg-Rhohtm1Hasu)
|
decreased mast cell degranulation
|
J:143491
|
Rhoqtm1b(EUCOMM)Hmgu/Rhoqtm1b(EUCOMM)Hmgu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)
|
abnormal axon extension
|
J:308705
|
abnormal microtubule cytoskeleton morphology
|
J:308705
|
Rhot1tm1.2Jmsu/Rhot1tm1.2Jmsu
(involves: 129 * 129S1/Sv * C57BL/6 * SJL)
|
abnormal mitochondrial physiology
|
J:216408
|
Rhot1tm1d(EUCOMM)Wtsi/Rhot1tm1d(EUCOMM)Wtsi
(involves: C57BL/6Dnk * C57BL/6N)
|
abnormal neuron mitochondrial morphology
|
J:240500
|
Rhox13tm1.2Chge/Y
(involves: 129P2/OlaHsd * C57BL/6N)
|
decreased male germ cell number
|
J:237048
|
increased male germ cell apoptosis
|
J:237048
|
oligozoospermia
|
J:237048
|
Rhox13tm1.2Chge/Y
(B6NCrl.129P2(Cg)-Rhox13tm1.2Chge)
|
decreased male germ cell number
|
J:237048
|
increased male germ cell apoptosis
|
J:237048
|
oligozoospermia
|
J:237048
|
Rhoxtm1.1Wilk/Rhoxtm1.1Wilk
(Not Specified)
|
decreased male germ cell number
|
J:229199
|
Rhoxtm1Wilk/Rhoxtm1Wilk Tg(RNU6-RNAi:Rhox3)2Wilk/0 Tg(Stra8-icre)1Reb/0
(involves: 129 * FVB/NJ)
|
decreased male germ cell number
|
J:229199
|
oligozoospermia
|
J:229199
|
Ric8atm1.1Zhua/Ric8atm1.1Zhua Tg(GFAP-cre)25Mes/0
(involves: FVB/N)
|
abnormal basement membrane morphology
|
J:191222
|
abnormal cerebellar granule cell migration
|
J:191222
|
Ric8atm1.1Zhua/Ric8atm1.1Zhua Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
abnormal basement membrane morphology
|
J:191222
|
Rictortm1.1Klg/Rictortm1.1Klg Tg(Mx1-cre)1Cgn/0
(B6.Cg-Rictortm1.1Klg Tg(Mx1-cre)1Cgn)
|
decreased T cell proliferation
|
J:189736
|
Rictortm1.1Mgn/Rictortm1.1Mgn Tg(Ins2-cre)25Mgn/0
(involves: 129S6/SvEvTac * BALB/c * C57BL/6 * DBA)
|
decreased pancreatic beta cell proliferation
|
J:170129
|
Rictortm1.2Mgn/Rictortm1.2Mgn
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL)
|
decreased cell proliferation
|
J:119564
|
Rif1Gt(A045A01)Wrst/Rif1Gt(A045A01)Wrst
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal mitosis
|
J:155449
|
decreased cell proliferation
|
J:155449
|
Rif1Gt(XT0278)Wtsi/Rif1Gt(XT0278)Wtsi
(involves: 129P2/OlaHsd * CD-1 * MF1)
|
abnormal DNA repair
|
J:195061
|
abnormal double-strand DNA break repair
|
J:195061
|
increased cellular sensitivity to ionizing radiation
|
J:195061
|
Rif1Gt(XT0278)Wtsi/Rif1Gt(XT0278)Wtsi Trp53bp1tm1Jc/Trp53bp1tm1Jc
(involves: 129P2/OlaHsd * CD-1 * MF1)
|
increased cellular sensitivity to ionizing radiation
|
J:195061
|
Rif1MommeD18/Rif1+ Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew
(involves: C57BL/6J * FVB/N)
|
abnormal epigenetic regulation of gene expression
|
J:201508
|
Rif1tm1.1Sbcb/Rif1tm1.1Sbcb
(involves: C57BL/6 * C57BL/6J)
|
decreased cell proliferation
|
J:155449
|
Rigitm1Aki/Rigitm1Aki
(involves: 129/Sv * C57BL/6)
|
abnormal cell physiology
|
J:137522
|
Rigitm1Aki/Rigitm1Aki Ifih1tm1Aki/Ifih1tm1Aki
(involves: 129/Sv * C57BL/6)
|
abnormal cell physiology
|
J:137522
|
Rimbp3tm1Gxu/Rimbp3tm1Gxu
(involves: 129/Sv * ICR)
|
abnormal sperm head morphology
|
J:144218
|
abnormal sperm nucleus morphology
|
J:144218
|
abnormal spermatid morphology
|
J:144218
|
detached acrosome
|
J:144218
|
detached sperm flagellum
|
J:144218
|
ectopic manchette
|
J:144218
|
kinked sperm flagellum
|
J:144218
|
oligozoospermia
|
J:144218
|
Rimklbem1Matak/Rimklbem1Matak
(C57BL/6J-Rimklbem1Matak)
|
abnormal sperm head morphology
|
J:303850
|
asthenozoospermia
|
J:303850
|
oligozoospermia
|
J:303850
|
Rin3tm1.1(KOMP)Vlcg/Rin3tm1.1(KOMP)Vlcg
(involves: 129P2/OlaHsd * C57BL/6N)
|
abnormal osteoblast physiology
|
J:358899
|
Riox1tm1Qch/Riox1tm1Qch Tg(Prrx1-cre)1Cjt/0
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl * SJL/J)
|
enhanced osteoblast differentiation
|
J:224562
|
Ripk1tm1.1Vmd/Ripk1tm1.1Vmd
(involves: C57BL/6N)
|
increased cell death
|
J:209137
|
increased thymocyte apoptosis
|
J:209137
|
Ripk1tm1Geno/Ripk1tm1Geno
(involves: C57BL/6)
|
decreased sensitivity to induced cell death
|
J:209137
|
Ripk2tm1Flv/Ripk2tm1Flv
(involves: 129S1/Sv)
|
decreased T cell proliferation
|
J:75400
|
Ripk2tm1Ghc/Ripk2tm1Ghc
(involves: 129S4/SvJae * C57BL/6)
|
decreased T cell proliferation
|
J:75401
|
Ripk3tm1Xidw/Ripk3tm1Xidw
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:157346
|
Ripk4tm1Pmh/Ripk4tm1Pmh
(involves: 129 * C57BL/6)
|
abnormal actin cytoskeleton morphology
|
J:259661
|
abnormal keratinocyte differentiation
|
J:259661,
J:78593
|
Ripply3tm1Sjt/Ripply3tm1Sjt
(involves: 129S1/Sv * C57BL/6)
|
abnormal neural crest cell migration
|
J:167713
|
abnormal vascular regression
|
J:167713
|
increased pancreatic beta cell proliferation
|
J:214095
|
Rit1tm1Dand/Rit1tm1Dand
(involves: 129S6/SvEvTac * Black Swiss)
|
increased cellular sensitivity to hydrogen peroxide
|
J:183038
|
Rlimtm1.1Inba/Rlimtm1.2Inba
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:165550
|
Rln1tm1Wint/Rln1tm1Wint
(involves: 129S1/Sv * C57BL/6J)
|
increased apoptosis
|
J:84575
|
oligozoospermia
|
J:84575
|
Rnase9tm1.1Xen/Rnase9tm1.1Xen
(involves: 129S6/SvEvTac)
|
abnormal sperm motility
|
J:212760
|
Rnaseh1tm1Crh/Rnaseh1tm1Crh
(involves: 129X1/SvJ)
|
abnormal mitochondrial morphology
|
J:82764
|
abnormal respiratory electron transport chain
|
J:82764
|
decreased mitochondrial DNA content
|
J:82764
|
disorganized mitochondrial cristae
|
J:82764
|
increased embryonic tissue cell apoptosis
|
J:82764
|
increased mitochondrial size
|
J:82764
|
Rnaseh2atm1Crh/Rnaseh2atm1Crh Sting1tm1Gnb/Sting1tm1Gnb
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:232933
|
Rnaseh2btm1a(EUCOMM)Wtsi/Rnaseh2btm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
decreased cell proliferation
|
J:186180
|
decreased fibroblast proliferation
|
J:186986
|
Rnaseh2btm1a(EUCOMM)Wtsi/Rnaseh2btm1a(EUCOMM)Wtsi Trp53tm1Mlh/Trp53tm1Mlh
(involves: 129P2/OlaHsd * C57BL/6N)
|
abnormal cell nucleus morphology
|
J:186180
|
cellular phenotype
|
J:186180
|
chromosomal instability
|
J:186180
|
increased cellular sensitivity to alkylating agents
|
J:186180
|
Rnaseh2btm1c(EUCOMM)Wtsi/Rnaseh2btm1c(EUCOMM)Wtsi Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N * SJL)
|
decreased B cell proliferation
|
J:186986
|
Rnaseh2btm1Hgu/Rnaseh2btm1Hgu
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell morphology
|
J:186180
|
Rnaseltm1Slvm/Rnaseltm1Slvm
(involves: 129P2/OlaHsd)
|
decreased T cell apoptosis
|
J:44292
|
Rnd2tm1.1Fgu/Rnd2tm1.1Fgu
(Not Specified)
|
abnormal cerebellar granule cell migration
|
J:344858
|
increased neuron apoptosis
|
J:344858
|
Rnf2tm1Mvi/Rnf2tm1Mvi Tg(Nes-cre/ERT2)5-1Imayo/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal neuron differentiation
|
J:154927
|
Rnf4Gt(ROSABetageo)1Gel/Rnf4Gt(ROSABetageo)1Gel
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal DNA methylation
|
J:163687
|
Rnf7Gt(XE423)Byg/Rnf7Gt(XE423)Byg
(involves: 129P2/OlaHsd)
|
increased apoptosis
|
J:164457
|
increased cellular sensitivity to ionizing radiation
|
J:164457
|
oxidative stress
|
J:164457
|
Rnf7Gt(XE423)Byg/Rnf7Gt(XE423)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle
|
J:178926
|
abnormal cell differentiation
|
J:178926
|
decreased cell proliferation
|
J:178926
|
increased embryonic tissue cell apoptosis
|
J:178926
|
increased spinal cord apoptosis
|
J:178926
|
Rnf7tm1c(EUCOMM)Wtsi/Rnf7tm1c(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal neuronal migration
|
J:205551
|
Rnf7tm1c(EUCOMM)Wtsi/Rnf7tm1c(EUCOMM)Wtsi Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6N * SJL)
|
decreased cerebellar granule cell precursor proliferation
|
J:205551
|
Rnf8Gt(AS0574)Wtsi/Rnf8+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cellular sensitivity to gamma-irradiation
|
J:161240
|
Rnf8Gt(AS0574)Wtsi/Rnf8Gt(AS0574)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal spermatocyte morphology
|
J:161240
|
azoospermia
|
J:161240
|
decreased fibroblast proliferation
|
J:161240
|
decreased spermatogonia number
|
J:161240
|
increased cellular sensitivity to gamma-irradiation
|
J:161240
|
increased thymocyte apoptosis
|
J:161240
|
induced chromosome breakage
|
J:161240
|
oligozoospermia
|
J:161240
|
spontaneous chromosome breakage
|
J:161240
|
Rnf8Gt(RRR260)Byg/Rnf8Gt(RRR260)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal spermatocyte morphology
|
J:161240
|
azoospermia
|
J:161240
|
decreased fibroblast proliferation
|
J:161240
|
decreased spermatogonia number
|
J:161240
|
increased cellular sensitivity to gamma-irradiation
|
J:161240
|
increased thymocyte apoptosis
|
J:161240
|
induced chromosome breakage
|
J:161240
|
oligozoospermia
|
J:161240
|
spontaneous chromosome breakage
|
J:161240
|
Rnf17em1Shnk/Rnf17em1Shnk
(C57BL/6-Rnf17em1Shnk)
|
abnormal male meiosis
|
J:334463
|
Rnf17tm1Jw/Rnf17tm1Jw
(involves: 129 * C57BL/6)
|
azoospermia
|
J:101737
|
Rnf19aGt(OST244733)Lex/Rnf19aGt(OST244733)Lex
(B6.129S5-Rnf19aGt(OST244733)Lex)
|
abnormal neuron proliferation
|
J:250032
|
Rnf20Gt(RRJ249)Byg/Rnf20+
(involves: 129P2/OlaHsd)
|
oxidative stress
|
J:268221
|
Rnf43em2Mage/Rnf43em2Mage
(Not Specified)
|
abnormal cell nucleus morphology
|
J:285428
|
Rnf43tm1Cle/Rnf43tm1Cle Znrf3tm1Cle/Znrf3tm1Cle Tg(Vil1-cre/ERT2)23Syr/0
(involves: C57BL/6 * DBA/2)
|
abnormal small intestinal crypt cell proliferation
|
J:186765
|
Rnf111em1Fzh/Rnf111+
(C57BL/6J-Rnf111em1Fzh)
|
decreased oocyte number
|
J:361059
|
Rnf111em2Fzh/Rnf111+
(C57BL/6J-Rnf111em2Fzh)
|
abnormal oocyte morphology
|
J:361059
|
decreased oocyte number
|
J:361059
|
Rnf114em1Nju/Rnf114em1Nju
(involves: C57BL/6J * DBA/2J)
|
decreased oocyte number
|
J:309826
|
maternal effect
|
J:309826
|
Rnf126tm1.1Bcgen/Rnf126tm1.1Bcgen
(FVB.B6(Cg)-Rnf126tm1.1Bcgen)
|
increased cellular sensitivity to ionizing radiation
|
J:344817
|
Rnf128tm1.1Flv/Y
(involves: 129S6/SvEvTac * C57BL/6)
|
increased T cell proliferation
|
J:153216
|
Rnf128tm1.1Flv/Y Tg(TcraTcrb)425Cbn/0
(involves: 129S6/SvEvTac * BALB/c * C57BL/6)
|
decreased T cell proliferation
|
J:153216
|
Rnf128tm1.1Flv/Rnf128tm1.1Flv
(involves: 129S6/SvEvTac * C57BL/6)
|
increased T cell proliferation
|
J:153216
|
Rnf128tm1.1Flv/Rnf128tm1.1Flv Tg(TcraTcrb)425Cbn/0
(involves: 129S6/SvEvTac * BALB/c * C57BL/6)
|
decreased T cell proliferation
|
J:153216
|
Rnf128tm1Cdon/Rnf128tm1Cdon
(involves: C57BL/6)
|
increased T cell proliferation
|
J:160681
|
Rnf128tm1Cdon/Rnf128tm1Cdon
(involves: 129 * C57BL/6)
|
increased splenocyte proliferation
|
J:160681
|
Rnf128tm1Cdon/Rnf128tm1Cdon Tg(TcraTcrb)425Cbn/0
(involves: 129 * BALB/c * C57BL/6)
|
increased splenocyte proliferation
|
J:160681
|
Rnf133em1Zuk/Rnf133em1Zuk
(involves: 129S5/SvEvBrd * C57BL/6NCrl * DBA/2NCrl)
|
abnormal sperm head morphology
|
J:330415
|
abnormal sperm motility
|
J:330415
|
asthenozoospermia
|
J:330415
|
decreased hyperactivated sperm motility
|
J:330415
|
decreased sperm progressive motility
|
J:330415
|
hairpin sperm flagellum
|
J:330415
|
kinked sperm flagellum
|
J:330415
|
teratozoospermia
|
J:330415
|
Rnf133em1Zuk/Rnf133em1Zuk Rnf148em2Zuk/Rnf148em2Zuk
(involves: 129S5/SvEvBrd * C57BL/6NCrl * DBA/2NCrl)
|
abnormal sperm head morphology
|
J:330415
|
asthenozoospermia
|
J:330415
|
decreased hyperactivated sperm motility
|
J:330415
|
decreased sperm progressive motility
|
J:330415
|
hairpin sperm flagellum
|
J:330415
|
teratozoospermia
|
J:330415
|
Rnf138tm1.1Lwan/Rnf138tm1.1Lwan
(Not Specified)
|
abnormal spermatocyte morphology
|
J:315603
|
abnormal spermatogonia morphology
|
J:315603
|
increased testis apoptosis
|
J:315603
|
oligozoospermia
|
J:315603
|
Rnf139tm1(KOMP)Wtsi/Rnf139tm1(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
increased hepatocyte apoptosis
|
J:231404
|
Rnf146tm1.1Rtpl/Rnf146tm1.1Rtpl Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:243612
|
Rnf146tm1.1Rtpl/Rnf146tm1.1Rtpl Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
(involves: C57BL/6J * CD-1)
|
decreased osteoblast proliferation
|
J:244583
|
impaired osteoblast differentiation
|
J:244583
|
Rnf149em1Staa/Rnf149em1Staa
(involves: BALB/c * C57BL/6)
|
abnormal fibroblast physiology
|
J:335358
|
increased cell proliferation
|
J:335358
|
Rnf152em1Pwa/Rnf152em1Pwa
(Not Specified)
|
abnormal fibroblast physiology
|
J:298778
|
Rnf168Gt(156B6)Cmhd/Rnf168Gt(156B6)Cmhd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:198260
|
abnormal male germ cell morphology
|
J:198260
|
chromosomal instability
|
J:198260
|
decreased male germ cell number
|
J:198260
|
increased cellular sensitivity to ionizing radiation
|
J:198260
|
increased cellular sensitivity to ultraviolet irradiation
|
J:198260
|
Rnf168Gt(405F11)Cmhd/Rnf168Gt(405F11)Cmhd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:198260
|
abnormal male germ cell morphology
|
J:198260
|
chromosomal instability
|
J:198260
|
decreased male germ cell number
|
J:198260
|
increased cellular sensitivity to ionizing radiation
|
J:198260
|
increased cellular sensitivity to ultraviolet irradiation
|
J:198260
|
Rnf186em1Ktak/Rnf186em1Ktak
(involves: C57BL/6 * DBA/2)
|
increased endoplasmic reticulum stress
|
J:258197
|
increased enterocyte apoptosis
|
J:258197
|
Rnf186tm1Ktak/Rnf186tm1Ktak
(involves: 129S4/SvJae * C57BL/6)
|
increased endoplasmic reticulum stress
|
J:258197
|
increased enterocyte apoptosis
|
J:258197
|
Rnf212repro57/Rnf212repro57
(B6;C3Fe-Rnf212repro57/J)
|
abnormal germ cell morphology
|
J:92463
|
arrest of male meiosis
|
J:92463
|
azoospermia
|
J:92463
|
Rnf212tm1Nhtr/Rnf212tm1Nhtr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal male meiosis
|
J:187173
|
Rnf216em1Lijd/Rnf216em1Lijd
(involves: C57BL/6)
|
abnormal spermatocyte morphology
|
J:307636
|
arrest of male meiosis
|
J:307636
|
decreased male germ cell number
|
J:307636
|
increased male germ cell apoptosis
|
J:307636
|
oligozoospermia
|
J:307636
|
Rnf216tm1b(EUCOMM)Wtsi/Rnf216tm1b(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal spermatocyte morphology
|
J:274674
|
decreased elongated spermatid number
|
J:274674
|
decreased male germ cell number
|
J:274674
|
increased male germ cell apoptosis
|
J:274674
|
Rnh1tm1Rall/Rnh1tm1Rall
(involves: 129S/SvEv * C57BL/6)
|
abnormal translation
|
J:261784
|
Rnu11tm1.1Rank/Rnu11tm1.1Rank Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas * 129X1/SvJ)
|
decreased radial glial cell number
|
J:266583
|
increased cell death
|
J:266583
|
Ro60tm1Woln/Ro60tm1Woln
(B6.129S1-Ro60tm1Woln)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:84627
|
Robo1tm1.1Ljr/Robo1tm1.1Ljr
(B6.129-Robo1tm1.1Ljr)
|
abnormal axon extension
|
J:109478
|
abnormal axon guidance
|
J:109478
|
enhanced neuronal migration
|
J:109478
|
Robo1tm1Matl/Robo1tm1Matl
(involves: CD-1)
|
abnormal axon guidance
|
J:89780
|
Robo1tm1Matl/Robo1tm1Matl
(involves: 129X1/SvJ)
|
increased mammary gland epithelial cell proliferation
|
J:141875
|
Robo1tm1Matl/Robo1tm1Matl Robo2tm1Mrt/Robo2tm1Mrt
(involves: 129P2/OlaHsd)
|
abnormal axon guidance
|
J:119469
|
decreased cell migration
|
J:193400
|
Robo1tm1Matl/Robo1tm1Matl Robo2tm1Mrt/Robo2tm1Mrt
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
abnormal axon guidance
|
J:120131
|
Robo1tm1Matl/Robo1tm1Matl Robo3tm1Matl/Robo3tm1Matl
(involves: 129/Sv * CD-1)
|
abnormal axon guidance
|
J:89438
|
Robo2tm1Mrt/Robo2tm1Mrt
(Not Specified)
|
abnormal axon guidance
|
J:89780
|
Robo2tm1Mrt/Robo2tm1Mrt Robo3tm1Matl/Robo3tm1Matl
(involves: 129/Sv * CD-1)
|
abnormal axon guidance
|
J:89438
|
Robo3tm1Matl/Robo3tm1Matl
(either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * CD-1))
|
abnormal axon guidance
|
J:89438
|
Robo3tm1Matl/Robo3tm1Matl Slit1tm1.1Matl/Slit1tm1.1Matl
(involves: 129/Sv * CD-1)
|
abnormal axon guidance
|
J:89438
|
Robo3tm1Matl/Robo3tm1Matl Slit1tm1.1Matl/Slit1tm1.1Matl Slit2tm1Matl/Slit2tm1Matl
(involves: 129/Sv * CD-1)
|
abnormal axon guidance
|
J:89438
|
Robo3tm1Matl/Robo3tm1Matl Slit2tm1Matl/Slit2tm1Matl
(involves: 129/Sv * CD-1)
|
abnormal axon guidance
|
J:89438
|
Robo4tm1Kzh/Robo4tm1Kzh
(involves: C57BL/6)
|
abnormal lung endothelial cell migration
|
J:133680
|
Rock1tm1.1Itl/Rock1tm1.1Itl
(Not Specified)
|
abnormal autophagy
|
J:207251
|
Rock1tm1.2Itl/Rock1tm1.2Itl
(Not Specified)
|
abnormal autophagy
|
J:207251
|
Rock1tm1Liao/Rock1+
(C57BL/6-Rock1tm1Liao)
|
abnormal leukocyte adhesion
|
J:135152
|
abnormal leukocyte migration
|
J:135152
|
impaired macrophage chemotaxis
|
J:135152
|
Rock2tm1.1Itl/Rock2+ Tg(Tagln-cre)1Her/0
(B6.Cg-Rock2tm1.1Itl Tg(Tagln-cre)1Her)
|
decreased vascular smooth muscle cell proliferation
|
J:222206
|
Rock2tm1Zpj/Rock2tm1Zpj
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal actin cytoskeleton morphology
|
J:225274
|
Ropn1Gt(OST21705)Lex/Ropn1Gt(OST21705)Lex
(involves: 129S5/SvEvBrd)
|
asthenozoospermia
|
J:206788
|
Ropn1Gt(OST21705)Lex/Ropn1Gt(OST21705)Lex Ropn1lGt(OST20298)Lex/Ropn1lGt(OST20298)Lex
(involves: 129S5/SvEvBrd)
|
immotile sperm
|
J:206788
|
Ropn1lGt(OST20298)Lex/Ropn1lGt(OST20298)Lex
(involves: 129S5/SvEvBrd)
|
abnormal respiratory motile cilium physiology
|
J:206788
|
Ror1tm1Ymi/Ror1tm1Ymi
(involves: 129P2/OlaHsd)
|
abnormal axon fasciculation
|
J:232175
|
Ror2tm1Anec/Ror2tm1Anec
(B6.129S1-Ror2tm1Anec)
|
oligozoospermia
|
J:134490
|
Ror2tm1Ymi/Ror2tm1Ymi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal primordial germ cell migration
|
J:179805
|
decreased primordial germ cell number
|
J:179805
|
Ror2Y324C/Ror2Y324C
(involves: C57BL/6J)
|
abnormal primordial germ cell migration
|
J:179805
|
decreased primordial germ cell number
|
J:179805
|
increased primordial germ cell apoptosis
|
J:179805
|
Rorasg/Rorasg
(involves: C57BL)
|
abnormal Purkinje cell differentiation
|
J:5968
|
Roratmgc26/Roratmgc26
(involves: D7R75M)
|
abnormal neuron proliferation
|
J:171777
|
abnormal radial glial cell morphology
|
J:171777
|
decreased cerebellar granule cell precursor proliferation
|
J:171777
|
Rorctm1Amj/Rorctm1Amj
(either: (involves: 129/Sv * C57BL/6) or (involves: 129/Sv * C57BL/6 * DBA/2))
|
increased T cell apoptosis
|
J:64381
|
Rorctm1Litt/Rorctm1Litt
(involves: 129P2/OlaHsd)
|
abnormal cell cycle
|
J:248565
|
increased thymocyte apoptosis
|
J:248565
|
Rorctm2Litt/Rorctm2Litt
(involves: 129P2/OlaHsd)
|
increased thymocyte apoptosis
|
J:87395
|
Ros1tm1.1Char/Ros1tm1.1Char
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J * SJL)
|
asthenozoospermia
|
J:211844
|
decreased sperm progressive motility
|
J:211844
|
hairpin sperm flagellum
|
J:211844
|
Ros1tm1Cbm/Ros1tm1Cbm
(involves: 129P2/OlaHsd)
|
impaired sperm migration in female genital tract
|
J:33259
|
Ros1tm1Cbm/Ros1tm1Cbm
(involves: 129P2/OlaHsd * C57BL/6)
|
asthenozoospermia
|
J:63727
|
hairpin sperm flagellum
|
J:63727
|
impaired sperm migration in female genital tract
|
J:63727
|
Ros1tm2Cbm/Ros1tm2Cbm
(involves: 129P2/OlaHsd)
|
impaired sperm migration in female genital tract
|
J:33259
|
Rpa1tm1Wed/Rpa1+
(involves: 129/Sv * C57BL/6J * SJL)
|
chromosome breakage
|
J:99303
|
Rpa1tm1Wed/Rpa1tm1Wed
(involves: 129/Sv * C57BL/6J * SJL)
|
decreased cell proliferation
|
J:99303
|
Rpap3tm1c(KOMP)Wtsi/Rpap3tm1c(KOMP)Wtsi Tg(Vil1-cre/ERT2)23Syr/0
(involves: C57BL/6N * DBA/2)
|
abnormal small intestine goblet cell morphology
|
J:314346
|
Rpl10aem2Mbar/Rpl10aem2Mbar
(C57BL/6-Rpl10aem2Mbar)
|
abnormal respiratory motile cilium morphology
|
J:328993
|
Rpl10lem1Qsh/Rpl10lem1Qsh
(involves: C57BL/6 * DBA/2J)
|
arrest of male meiosis
|
J:319673
|
azoospermia
|
J:319673
|
increased male germ cell apoptosis
|
J:319673
|
Rpl13atm1.1Jesc/Rpl13atm1.1Jesc
(FVB.129S5(Cg)-Rpl13atm1.1Jesc)
|
abnormal oxidative phosphorylation
|
J:237822
|
abnormal redox activity
|
J:237822
|
Rpl13atm1.1Mazu/Rpl13atm1.1Mazu Lyz2tm1(cre)Ifo/Lyz2+
(involves: C57BL/6)
|
abnormal macrophage chemotaxis
|
J:194920
|
Rpl22Gt(GST000137)Lex/Rpl22Gt(GST000137)Lex
(involves: 129S5/SvEvBrd)
|
increased T cell apoptosis
|
J:123569
|
Rpl24Bst/Rpl24+
(involves: C57BLKS)
|
abnormal cell cycle
|
J:92052
|
abnormal cell physiology
|
J:92052
|
Rpl27aSfa/Rpl27a+
(C57BL/6J-Rpl27aSfa)
|
increased hematopoietic stem cell proliferation
|
J:174216
|
Rpl29tm1Udel/Rpl29tm1Udel
(129S6/SvEvTac-Rpl29tm1Udel)
|
abnormal cell cycle
|
J:117229
|
decreased fibroblast proliferation
|
J:117229
|
Rpl38Ts/Rpl38Ts
(BALB/c-Rpl38Ts)
|
abnormal nucleolus morphology
|
J:6315
|
Rpl39lem1Hqi/Rpl39lem1Hqi
(involves: C57BL/6J)
|
abnormal male germ cell physiology
|
J:317811
|
abnormal sperm axoneme morphology
|
J:317811
|
abnormal sperm flagellum morphology
|
J:317811
|
abnormal sperm mitochondrial sheath morphology
|
J:317811
|
abnormal spermatogonia proliferation
|
J:317811
|
asthenozoospermia
|
J:317811
|
decreased spermatogonia number
|
J:317811
|
increased testis apoptosis
|
J:317811
|
oligozoospermia
|
J:317811
|
oxidative stress
|
J:317811
|
teratozoospermia
|
J:317811
|
Rprd1btm1Tshu/Rprd1btm1Tshu Tg(Vil1-cre)20Syr/0
(involves: C57BL/6 * DBA/2)
|
abnormal large intestine goblet cell morphology
|
J:300857
|
abnormal small intestine goblet cell morphology
|
J:300857
|
Rps2tm1.1Geno/Rps2+
(B6.129(Cg)-Rps2tm1.1Geno)
|
oxidative stress
|
J:321029
|
Rps6tm1Gtho/Rps6tm1Gtho Tg(Mx1-cre)1Cgn/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal cell cycle
|
J:62795
|
abnormal cell morphology
|
J:62795
|
Rps6tm1Om/Rps6tm1Om
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
abnormal cell cycle
|
J:100952
|
abnormal cell morphology
|
J:100952
|
abnormal cell physiology
|
J:100952
|
Rps6ka3tm1.1Kry/Rps6ka3+
(involves: 129X1/SvJ)
|
abnormal osteoblast physiology
|
J:89403
|
Rps6ka3tm1.1Kry/Rps6ka3tm1.1Kry
(involves: 129X1/SvJ)
|
abnormal osteoblast physiology
|
J:89403
|
Rps6ka4tm1Jsca/Rps6ka4tm1Jsca Rps6ka5tm1Jsca/Rps6ka5tm1Jsca
(Not Specified)
|
decreased T cell proliferation
|
J:124301
|
Rps6ka5tm1Jsca/Rps6ka5tm1Jsca
(Not Specified)
|
increased susceptibility to neuronal excitotoxicity
|
J:172062
|
Rps6kb1tm1Gtho/Rps6kb1tm1Gtho Rps6kb2tm1Gtho/Rps6kb2tm1Gtho
(involves: 129P2/OlaHsd)
|
abnormal cellular respiration
|
J:129852
|
abnormal mitochondrial morphology
|
J:129852
|
increased fatty acid beta-oxidation
|
J:129852
|
Rps7Zma/Rps7+
(involves: BALB/c * C3H/HeH * C57BL/6J)
|
increased neuron apoptosis
|
J:195156
|
Rps9tm1.1Geno/Rps9tm1.1Geno
(involves: C57BL/6)
|
abnormal lipid oxidation
|
J:329922
|
oxidative stress
|
J:329922
|
Rps12-ps1/Xisttm1.1Nbd/Rps12-ps1+
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:85305
|
Rps12-ps1/Xisttm1.1Nbd/Xist+
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:85305
|
Rps12-ps1/Xisttm1Nbd/Rps12-ps1+
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:85305
|
Rps12-ps1/Xisttm1Nbd/Xist+
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:85305
|
Rps12em1.1Nbakr/Rps12+
(involves: C57BL/6J * FVB/N)
|
abnormal hematopoietic stem cell proliferation
|
J:338970
|
Rps14tm1.1Ble/Rps14+ Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6J * C57BL/6NTac * CBA/J)
|
abnormal cell cycle
|
J:233322
|
abnormal translation
|
J:233322
|
decreased telomere length
|
J:233322
|
increased apoptosis
|
J:233322
|
Rps19Mhdadsk3/Rps19+
(C3HeB/FeJ-Rps19Mhdadsk3/Ieg)
|
increased apoptosis
|
J:139244
|
Rps26tm1.1Jzc/Rps26tm1.1Jzc Tg(Gdf9-icre)5092Coo/0
(involves: C57BL/6 * C57BL/6J)
|
abnormal oocyte morphology
|
J:278629
|
absent oocytes
|
J:278629
|
Rps26tm1.1Jzc/Rps26tm1.1Jzc Tg(Zp3-cre)93Knw/0
(involves: C57BL/6J)
|
abnormal oocyte morphology
|
J:278629
|
Rps27lGt(IST11658B7)Tigm/Rps27lGt(IST11658B7)Tigm
(C57BL/6-Rps27lGt(IST11658B7)Tigm)
|
increased thymocyte apoptosis
|
J:223276
|
Rps27lGt(IST11658B7)Tigm/Rps27lGt(IST11658B7)Tigm Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas * C57BL/6N)
|
aneuploidy
|
J:223276
|
chromosomal instability
|
J:223276
|
Rptortm1.1Dmsa/Rptortm1.1Dmsa Tg(Amh-cre)8815Reb/0
(involves: 129S/SvEv * 129S1/SvImJ * C57BL/6 * FVB/N)
|
abnormal cell cytoskeleton morphology
|
J:268375
|
abnormal male germ cell physiology
|
J:268375
|
azoospermia
|
J:268375
|
decreased elongated spermatid number
|
J:268375
|
decreased male germ cell number
|
J:268375
|
decreased round spermatid number
|
J:268375
|
decreased spermatid number
|
J:268375
|
increased testis apoptosis
|
J:268375
|
Rptortm1.1Rueg/Rptor+
(involves: 129S1/SvImJ * BALB/cJ * C57BL/6J)
|
abnormal cell differentiation
|
J:143749
|
Rptortm1Lex/Rptortm1Lex
(involves: 129S/SvEvBrd)
|
decreased inner cell mass proliferation
|
J:137592
|
Rptortm1Rueg/Rptortm1Rueg Tg(ACTA1-cre)1Mll/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal muscle cell glucose uptake
|
J:143748
|
Rr27tm1.1Kpfe/Rr27+
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal DNA methylation
|
J:82798
|
Rr27tm1.1Mnn/Rr27+
(involves: 129S1/Sv * CAST/Ei * FVB/NJ * Swiss)
|
abnormal imprinting
|
J:308869
|
Rr27tm1.1Msb/Rr27+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal imprinting
|
J:52162,
J:106218,
J:105567
|
Rr27tm1Kpfe/Rr27tm1Kpfe Tg(CD2-cre)1Sriv/?
(involves: 129S1/Sv * 129X1/SvJ)
|
cellular phenotype
|
J:82595
|
Rr27tm1Kpfe/Rr27tm1Kpfe Tg(Ckmm-cre)5Khn/0
(involves: 129S1/Sv * 129X1/SvJ * FVB)
|
abnormal imprinting
|
J:82798
|
Rr27tm1Pes/Rr27+
(involves: 129S1/SvImJ * FVB/N-Chr 7CAST/Ei/J)
|
paternal imprinting
|
J:91020
|
Rr27tm1Rohl/Rr27+
(involves: 129S1/Sv * 129X1/SvJ * FVB/N * SD7)
|
abnormal imprinting
|
J:82427
|
Rr27tm1Tilg/Rr27+
(involves: 129S1/Sv)
|
abnormal imprinting
|
J:81888
|
Rr27tm2.1Pes/Rr27+
(involves: 129S1/Sv * 129S1/SvImJ * CAST/Ei * FVB/NJ)
|
cellular phenotype
|
J:195982
|
Rr27tm2Msb/Rr27+ Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129P2/OlaHsd * C57BL/6 * DBA)
|
paternal imprinting
|
J:105567
|
Rr27tm2Tilg/Rr27+
(involves: 129S1/Sv)
|
cellular phenotype
|
J:86440
|
Rr27tm3Msb/Rr27+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal imprinting
|
J:106218
|
Rr27tm4Msb/Rr27+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal imprinting
|
J:106218
|
Rr27tm5.1Msb/Rr27+
(involves: 129P2/OlaHsd * C57BL/6 * M. m. castaneus)
|
abnormal imprinting
|
J:173610
|
Rr27tm6.1Msb/Rr27+
(involves: 129P2/OlaHsd * C57BL/6 * M. m. castaneus)
|
abnormal imprinting
|
J:173610
|
Rr28tm1Msb/Rr28+
(involves: 129P2/OlaHsd * C57BL/6 * M. m. castaneus)
|
cellular phenotype
|
J:118894
|
Rr28tm1Tilg/Rr28+ Igf2tm1Rob/Igf2+
(involves: 129S/SvEv * 129S1/Sv * C57BL/6J)
|
abnormal fetal cardiomyocyte proliferation
|
J:77413
|
increased hepatocyte proliferation
|
J:77413
|
Rr70tm1Alb/Rr70+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal DNA methylation
|
J:105289
|
genetic imprinting
|
J:105289
|
Rr70tm1Alb/Rr70tm1Alb
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal DNA methylation
|
J:113402
|
abnormal imprinting
|
J:113402
|
Rr129tm4Msb/Rr129+
(involves: 129P2/OlaHsd * C57BL/6J)
|
cellular phenotype
|
J:106218
|
Rr161tm2.2Wtg/Rr161tm2.2Wtg
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6)
|
abnormal DNA methylation
|
J:167472
|
Rr170tm1.1Iku/Rr170tm1.1Iku
(B6.Cg-Rr170tm1.1Iku)
|
decreased T cell proliferation
|
J:333539
|
increased T cell apoptosis
|
J:333539
|
Rr198em1Takas/Rr198+
(involves: C57BL/6 * DBA/2 * JF1)
|
abnormal epigenetic regulation of gene expression
|
J:241393
|
cellular phenotype
|
J:241393
|
Rr199em1Takas/Rr199+
(involves: C57BL/6 * DBA/2 * JF1)
|
abnormal epigenetic regulation of gene expression
|
J:241393
|
cellular phenotype
|
J:241393
|
Rr200em1Takas/Rr200+
(involves: C57BL/6 * DBA/2 * JF1)
|
abnormal epigenetic regulation of gene expression
|
J:241393
|
cellular phenotype
|
J:241393
|
Rr272em1Issa/Rr272em1Issa
(involves: C57BL/6J * DBA/2J)
|
cellular phenotype
|
J:333875
|
Rr273em1Issa/Rr273em1Issa
(involves: C57BL/6J * DBA/2J)
|
decreased cell proliferation
|
J:333875
|
Rr395em1Bhao/Rr395em1Bhao
(Not Specified)
|
increased thymocyte apoptosis
|
J:333961
|
Rr401em1Yushi/Rr401em1Yushi
(Not Specified)
|
oligozoospermia
|
J:334319
|
Rr504em2Takas/Rr504em2Takas
(C57BL/6J-Rr504em2Takas)
|
oligozoospermia
|
J:334329
|
Rr504em4Takas/Rr504em4Takas
(C57BL/6J-Rr504em4Takas)
|
oligozoospermia
|
J:334329
|
Rragatm1.1Dmsa/Rragatm1.1Dmsa
(involves: 129 * C57BL/6 * C57BL/6J)
|
abnormal autophagy
|
J:194401
|
Rragcem1Efe/Rragc+
(Not Specified)
|
abnormal fibroblast physiology
|
J:320567
|
decreased B cell proliferation
|
J:320567
|
Rras2Gt(OST361011)Lex/Rras2+
(involves: 129S5/SvEvBrd)
|
maternal effect
|
J:151653
|
Rras2Gt(OST361011)Lex/Rras2Gt(OST361011)Lex
(involves: 129S5/SvEvBrd)
|
decreased B cell proliferation
|
J:151653
|
maternal effect
|
J:151653
|
Rreb1em1Rtpl/Rreb1+
(C57BL/6J-Rreb1em1Rtpl)
|
increased cell proliferation
|
J:296982
|
Rrm2bGt(OST85254)Lex/Rrm2bGt(OST85254)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
increased kidney apoptosis
|
J:186071
|
increased kidney cell proliferation
|
J:186071
|
increased renal tubule apoptosis
|
J:186071
|
Rrm2btm1Ynak/Rrm2btm1Ynak
(involves: 129 * C57BL/6J)
|
increased kidney apoptosis
|
J:84841
|
Rrn3tm1.1Igt/Rrn3tm1.1Igt
(involves: 129/Sv * C57BL/6)
|
cellular phenotype
|
J:99711
|
Rrn3tm1.1Igt/Rrn3tm1.1Igt Tg(Slc6a3-cre/ERT2)1Span/0
(involves: 129/Sv * C57BL/6)
|
abnormal cell physiology
|
J:242309
|
abnormal mitochondrial morphology
|
J:168232
|
abnormal nucleolus morphology
|
J:242309
|
increased cellular sensitivity to oxidative stress
|
J:168232
|
oxidative stress
|
J:168232
|
Rrn3tm1.1Igt/Rrn3tm1.1Igt Tg(Slc6a3-icre)9190Gsc/0
(involves: 129/Sv * C57BL/6 * FVB/N)
|
abnormal nucleolus morphology
|
J:168232
|
Rrn3tm1.2Igt/Rrn3tm1.2Igt
(involves: 129/Sv * C57BL/6 * SJL)
|
increased neural tube apoptosis
|
J:99711
|
Rsf1tm1c(EUCOMM)Wtsi/Rsf1tm1c(EUCOMM)Wtsi Tg(Nes-cre)1Kln/0
(involves: C57BL/6N * SJL)
|
abnormal double-strand DNA break repair
|
J:267928
|
decreased neuron apoptosis
|
J:267928
|
rsph/rsph
(involves: 129S4/SvJae * C57BL/6J)
|
globozoospermia
|
J:60747
|
Rsph1tm1Htan/Rsph1tm1Htan
(involves: 129S1/Sv * C57BL/6J)
|
abnormal sperm flagellum morphology
|
J:138122
|
abnormal sperm head morphology
|
J:138122
|
abnormal spermatid morphology
|
J:138122
|
oligozoospermia
|
J:138122
|
Rsph6aem1Osb/Rsph6aem1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal manchette disassembly
|
J:266136
|
abnormal sperm axoneme morphology
|
J:266136
|
abnormal sperm fibrous sheath morphology
|
J:266136
|
abnormal sperm head morphology
|
J:266136
|
abnormal sperm mitochondrial sheath morphology
|
J:266136
|
immotile sperm
|
J:266136
|
short sperm flagellum
|
J:266136
|
Rsph6aem2Osb/Rsph6aem2Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm head morphology
|
J:266136
|
immotile sperm
|
J:266136
|
short sperm flagellum
|
J:266136
|
Rsph9em1Jwji/Rsph9em1Jwji
(B6.Cg-Rsph9em1Jwji)
|
abnormal brain ependyma motile cilium morphology
|
J:294184
|
abnormal brain ependyma motile cilium physiology
|
J:294184
|
Rspo1tm1.1Ktom/Rspo1tm1.1Ktom
(involves: C57BL/6 * CBA)
|
decreased oocyte number
|
J:133934
|
Rspo1tm1Mcch/Rspo1tm1Mcch
(involves: 129 * C57BL/6J)
|
abnormal female meiosis
|
J:133933
|
Rspo1tm1Mcch/Rspo1tm1Mcch
(involves: 129/Sv * C57BL/6J)
|
abnormal germ cell morphology
|
J:203797
|
abnormal oogenesis
|
J:203797
|
decreased oocyte number
|
J:203797
|
Rtel1tm1Hdin/Rtel1tm1Hdin
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased DNA replication
|
J:202812
|
Rtel1tm1Pml/Rtel1tm1Pml
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell differentiation
|
J:91351
|
Rtel1tm2.1Hdin/Rtel1tm2.1Hdin
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:202812
|
abnormal mitosis
|
J:202812
|
abnormal telomere morphology
|
J:202812
|
cellular phenotype
|
J:202812
|
decreased DNA replication
|
J:202812
|
early cellular replicative senescence
|
J:202812
|
Rtel1tm2.1Hdin/Rtel1tm2.1Hdin Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6)
|
abnormal telomere morphology
|
J:202812
|
Rtel1tm3.1Hdin/Rtel1tm3.1Hdin
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
cellular phenotype
|
J:202812
|
Rtf2tm1c(KOMP)Wtsi/Rtf2tm1d(KOMP)Wtsi
(involves: C57BL/6 * C57BL/6N * FVB/N * SJL)
|
decreased DNA replication
|
J:360903
|
decreased fibroblast proliferation
|
J:360903
|
Rtl1tm1Fuis/Rtl1+
(involves: 129S/SvEv * C57BL/6)
|
abnormal basement membrane morphology
|
J:132647
|
Rtn2tm1Lex/Rtn2+
(involves: 129S/SvEvBrd)
|
decreased skeletal muscle cell glucose uptake
|
J:158249
|
Rtn2tm1Lex/Rtn2tm1Lex
(involves: 129S/SvEvBrd)
|
decreased skeletal muscle cell glucose uptake
|
J:158249
|
Rtn3tm1Yanr/Rtn3tm1Yanr
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal mitochondrial morphology
|
J:326034
|
cellular phenotype
|
J:217161
|
Rtn4Gt715Lex/Rtn4Gt715Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal axon extension
|
J:133355
|
Rtn4rtm1.1Pado/Rtn4rtm1.1Pado
(involves: 129S/SvEvBrd * 129S4/SvJae)
|
abnormal axon extension
|
J:138580
|
Rubcnlem1Qsun/Rubcnlem1Qsun Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(B6.Cg-Speer6-ps1Tg(Alb-cre)21Mgn Rubcnlem1Qsun)
|
impaired autophagy
|
J:272052
|
Runx1tm1(RUNX1)Gcg/Runx1tm1(RUNX1)Gcg Tg(Mx1-cre)1Cgn/0
(involves: 129S1/Sv * C57BL/6 * CBA)
|
abnormal granulocyte differentiation
|
J:106800
|
Runx1tm1Soga/Runx1tm1.1Soga Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal megakaryocyte differentiation
|
J:88511
|
Runx1tm1Yg/Runx1tm1Yg
(either: (involves: 129/Sv * 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1))
|
increased thymocyte apoptosis
|
J:125830
|
Runx1tm2.1Gss/Runx1tm2.1Gss
(involves: 129S4/SvJae * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:214025
|
Runx1tm3Dow/Runx1+ Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal cell physiology
|
J:77129
|
Runx2tm1Hkiy/Runx2+
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired osteoblast differentiation
|
J:223410
|
Runx2tm1Hkiy/Runx2tm1Hkiy
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired osteoblast differentiation
|
J:223410
|
Runx2tm1Jals/Runx2tm1Jals
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal osteoblast differentiation
|
J:143532
|
increased osteoblast proliferation
|
J:143532
|
Runx2tm1Kish/Runx2tm1Kish
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoblast differentiation
|
J:59821,
J:40783
|
abnormal osteoclast differentiation
|
J:59821,
J:40783
|
Runx2tm1Mjo/Runx2+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal osteoblast differentiation
|
J:40784
|
Runx3tm1Yg/Runx3tm1Yg
(either: (involves: 129S1/Sv * 129X1/SvJ * ICR) or (involves: 129S1/Sv * 129X1/SvJ * MF1))
|
abnormal dendritic cell differentiation
|
J:88424
|
Runx3tm1Yg/Runx3tm1Yg
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
decreased osteoblast proliferation
|
J:224290
|
Runx3tm2Yg/Runx3tm2Yg
(involves: 129S1/Sv * 129X1/SvJ * BALB/c * C57BL/6 * ICR)
|
abnormal dendritic cell differentiation
|
J:109584
|
Ruvbl1tm1.2Oxbk/Ruvbl1tm1.2Oxbk
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * SJL)
|
decreased inner cell mass proliferation
|
J:220926
|
Rxfp1tm1Jgo/Rxfp1tm1Jgo
(involves: 129S5/SvEvBrd * C57BL/6)
|
azoospermia
|
J:87579
|
Rxfp2m1Lja/Rxfp2m1Lja
(C57BL/6J-Rxfp2m1Lja)
|
decreased male germ cell number
|
J:166053
|
Rxfp2tm1Aia/crsp
(involves: 129S7/SvEvBrd * C57BL/6J * FVB/N)
|
azoospermia
|
J:79124
|
Rxfp2tm1Aia/Rxfp2tm1Aia
(involves: 129S7/SvEvBrd * C57BL/6J)
|
azoospermia
|
J:79124
|
Rxratm1Krc/Rxratm1Krc Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6)
|
impaired macrophage phagocytosis
|
J:168799
|
increased mesangial cell number
|
J:168799
|
increased renal glomerulus apoptosis
|
J:168799
|
Rxratm1Rev/Rxratm1Rev
(involves: 129S4/SvJae * C57BL/6)
|
decreased hepatocyte proliferation
|
J:18047
|
Rxratm2Ipc/Rxratm4Ipc Tg(KRT14-cre)1Ipc/0
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
increased keratinocyte proliferation
|
J:67149
|
Rxrbtm1Ipc/Rxrbtm1Ipc
(involves: 129S2/SvPas)
|
abnormal acrosome morphology
|
J:30560
|
abnormal sperm mitochondrial sheath morphology
|
J:30560
|
absent acrosome
|
J:30560
|
asthenozoospermia
|
J:30560
|
coiled sperm flagellum
|
J:30560
|
decreased germ cell number
|
J:30560
|
detached acrosome
|
J:30560
|
oligozoospermia
|
J:30560
|
teratozoospermia
|
J:30560
|
Rxrbtm1Mma/Rxrbtm1Mma
(involves: 129 * C57BL/6)
|
decreased cholesterol efflux
|
J:101966
|
Ryr1em1Zor/Ryr1em2Zor
(C57BL/6J-Ryr1em1Zor Ryr1em2Zor)
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:292405
|
Ryr1m1Nisw/Ryr1+
(129S1.B6-Ryr1m1Nisw)
|
abnormal mitochondrial physiology
|
J:219285
|
abnormal mitochondrial shape
|
J:219285
|
Ryr1tm1Alle/Ryr1tm1Alle
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell physiology
|
J:111187
|
Ryr2tm1.1Hta/Ryr2tm1.1Hta
(involves: 129S4/SvJae)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:48277
|
S1pr1tm1.1Thla/S1pr1tm1.1Thla
(B6.Cg-S1pr1tm1.1Thla)
|
abnormal leukocyte migration
|
J:163389
|
S1pr1tm1Rlp/S1pr1tm1Rlp
(involves: 129S6/SvEvTac * C57BL/6)
|
impaired fibroblast cell migration
|
J:71961
|
S1pr1tm1Rlp/S1pr1tm1Rlp
(involves: 129S6/SvEvTac)
|
increased neuron apoptosis
|
J:189010
|
increased vascular endothelial cell apoptosis
|
J:189010
|
S1pr2tm1Rlp/S1pr2tm1Rlp
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased B cell apoptosis
|
J:174313
|
increased B cell proliferation
|
J:174313
|
S1pr2tm1Ytak/S1pr2tm1Ytak
(involves: 129P2/OlaHsd * C57BL/6)
|
increased lung endothelial cell migration
|
J:168060
|
S1pr3tm1Jch/S1pr3tm1Jch
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)
|
abnormal cell physiology
|
J:71372
|
S100a1tm1Jhh/S100a1tm1Jhh
(involves: 129S1/Sv * C57BL/6)
|
increased lung endothelial cell apoptosis
|
J:230300
|
S100a4tm1.1Abres/S100a4tm1.1Abres
(B6.Cg-S100a4tm1.1Abres)
|
impaired macrophage chemotaxis
|
J:182865
|
S100a4tm1Amba/S100a4tm1Amba
(involves: A/Sn)
|
abnormal apoptosis
|
J:89563
|
S100a9tm1Nck/S100a9tm1Nck
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cellular extravasation
|
J:81642
|
Sac3d1tm1Hnaka/Sac3d1tm1Hnaka
(involves: 129P2/OlaHsd)
|
increased T cell proliferation
|
J:144601
|
Sacstm1(NCOM)Mfgc/Sacstm1(NCOM)Mfgc
(Not Specified)
|
abnormal mitochondrial physiology
|
J:182034
|
Safbtm1So/Safbtm1So
(involves: 129 * C57BL/6J)
|
azoospermia
|
J:97633
|
decreased male germ cell number
|
J:97633
|
increased male germ cell apoptosis
|
J:97633
|
Sall1tm1Ryn/Sall1tm1Ryn
(involves: 129S/SvEv * C57BL/6N)
|
increased metanephric mesenchyme apoptosis
|
J:71242
|
Sall1tm2Ryn/Sall1tm2Ryn
(involves: 129P2/OlaHsd * C57BL/6N)
|
increased metanephric mesenchyme apoptosis
|
J:71242
|
Sall1tm4.1Ryn/Sall1tm4.1Ryn Sall4tm3Ryn/Sall4tm4Ryn
(involves: 129P2/OlaHsd)
|
decreased cell proliferation
|
J:159449
|
Sall2tm1Jkoh/Sall2tm1Jkoh Sall4Gt(W097E01)Flo/Sall4+
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J)
|
increased embryonic neuroepithelium apoptosis
|
J:143350
|
Sall4tm1Ryn/Sall4tm1Ryn
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased inner cell mass proliferation
|
J:118119
|
Sall4tm1Yam/Sall4tm1Yam
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal cell physiology
|
J:158264
|
decreased cell proliferation
|
J:158264
|
decreased inner cell mass proliferation
|
J:158264
|
Samhd1tm1d(EUCOMM)Wtsi/Samhd1tm1d(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal cell physiology
|
J:202757
|
Samsn1tm1Xyw/Samsn1tm1Xyw
(B6.129P2-Samsn1tm1Xyw)
|
increased B cell proliferation
|
J:158032
|
increased T cell proliferation
|
J:158032
|
Saraftm1c(KOMP)Wtsi/Saraftm1c(KOMP)Wtsi Tg(Pgk1-cre)1Lni/0
(involves: 129S4/SvJaeSor * BALB/c * C57BL/6J * C57BL/6N)
|
abnormal cellular respiration
|
J:337869
|
decreased fibroblast proliferation
|
J:337869
|
decreased neuronal precursor proliferation
|
J:337869
|
Sarm1tm1.1Diam/Sarm1tm1.1Diam
(involves: 129X1/SvJ * C57BL/6)
|
decreased neuron apoptosis
|
J:196200
|
increased neuron apoptosis
|
J:200140
|
Sarm1tm1Aidi/Sarm1tm1Aidi
(involves: 129X1/SvJ * C57BL/6J)
|
decreased apoptosis
|
J:126083
|
Sash3tm1Hlz/Sash3tm1Hlz
(B6.129P2-Sash3tm1Hlz)
|
decreased T cell proliferation
|
J:102171
|
Sat1tm1Alh/Sat1tm1Alh
(B6.129X1-Sat1tm1Alh)
|
abnormal aerobic respiration
|
J:120870
|
Satb1tm1Kos/Satb1tm1Kos
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal T cell proliferation
|
J:61085
|
Satb2tm1Rug/Satb2tm1Rug
(Not Specified)
|
impaired osteoblast differentiation
|
J:115876
|
Sav1tm1.1Dupa/Sav1tm1.1Dupa Tg(Vil1-cre)997Gum/0
(involves: 129P2/OlaHsd * C57BL/6J * SJL)
|
abnormal enterocyte proliferation
|
J:165471
|
Sav1tm1.1Rjo/Sav1tm1.1Rjo Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * CD-1 * DBA * SJL)
|
increased hepatocyte proliferation
|
J:156531
|
Sav1tm1Dlim/Sav1tm1Dlim
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal enterocyte proliferation
|
J:134270
|
abnormal intestinal goblet cell morphology
|
J:134270
|
abnormal keratinocyte differentiation
|
J:134270
|
Saysd1em1Yogo/Saysd1em1Yogo
(C57BL/6N-Saysd1em1Yogo)
|
oligozoospermia
|
J:340694
|
Sbdsem1(SBDS*)Dbau/Sbdsem1(SBDS*)Dbau
(C57BL/6J-Sbdsem1(SBDS*)Dbau/Dbau)
|
abnormal ribosome biogenesis
|
J:335832
|
Sbdstm1Jrom/Sbdstm1Jrom
(involves: 129S6/SvEvTac * C57BL/6J)
|
absent inner cell mass proliferation
|
J:112167
|
Sbf1tm1Mlc/Sbf1tm1Mlc
(involves: C57BL/6)
|
azoospermia
|
J:76406
|
decreased elongated spermatid number
|
J:76406
|
decreased round spermatid number
|
J:76406
|
decreased spermatid number
|
J:76406
|
Sbno1tm1.1Hssk/Sbno1tm1.1Hssk
(involves: C57BL/6)
|
decreased cell proliferation
|
J:266780
|
increased apoptosis
|
J:266780
|
Sbno2tm1.1Aki/Sbno2tm1.1Aki
(involves: 129 * C57BL/6)
|
impaired osteoblast differentiation
|
J:202853
|
Sc5dtm1Fdp/Sc5dtm1Fdp
(involves: 129S1/Sv * 129X1/SvJ)
|
lysosomal protein accumulation
|
J:84450
|
Scaitm1b(EUCOMM)Hmgu/Scaitm1b(EUCOMM)Hmgu
(involves: C57BL/6N * FVB/N)
|
abnormal double-strand DNA break repair
|
J:240463
|
arrest of male meiosis
|
J:240463
|
cellular phenotype
|
J:240463
|
increased cellular sensitivity to ionizing radiation
|
J:240463
|
Scamp1tm1Sud/Scamp1tm1Sud
(involves: 129S6/SvEvTac)
|
abnormal cell physiology
|
J:58332
|
Scapertm1a(EUCOMM)Hmgu/Scapertm1a(EUCOMM)Hmgu
(involves: C57BL/6N)
|
azoospermia
|
J:294607
|
Scarb1tm1Kri/Scarb1tm1Kri
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cellular cholesterol metabolism
|
J:216748
|
abnormal female meiosis
|
J:216748
|
abnormal oocyte morphology
|
J:105226
|
oocyte degeneration
|
J:216748
|
Scarf1tm1Tkms/Scarf1tm1Tkms
(involves: C57BL/6)
|
abnormal cell physiology
|
J:208237
|
cellular phenotype
|
J:208237
|
impaired macrophage phagocytosis
|
J:208237
|
scb/scb
(C3H/HeH-scb)
|
abnormal chromosome morphology
|
J:4646
|
elevated level of mitotic sister chromatid exchange
|
J:4646
|
Scgb3a1tm1.1Shk/Scgb3a1tm1.1Shk
(B6N.Cg-Scgb3a1tm1.1Shk)
|
decreased respiratory motile cilia number
|
J:276140
|
Scgb3a2tm1.1Shk/Scgb3a2tm1.1Shk
(B6N.Cg-Scgb3a2tm1.1Shk)
|
decreased respiratory motile cilia number
|
J:276140
|
Schip1Gt(ROSA)77Sor/Schip1Gt(ROSA)77Sor
(involves: 129S4/SvJaeSor)
|
decreased fibroblast cell migration
|
J:117491
|
Scintm1Glog/Scintm1Glog Tg(Acp5-cre)4Rda/0
(either: (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * CBA))
|
abnormal osteoclast differentiation
|
J:223220
|
Scmh1tm1Hko/Scmh1tm1Hko
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
arrest of male meiosis
|
J:119909
|
azoospermia
|
J:119909
|
early cellular replicative senescence
|
J:119909
|
multinucleated giant male germ cells
|
J:119909
|
Scml1tm1.2Atot/Y
(STOCK Scml1tm1.2Atot/Atot)
|
abnormal spermatocyte morphology
|
J:278848
|
Scml2em1Shnk/Scml2em1Shnk
(C57BL/6J-Scml2em1Shnk)
|
azoospermia
|
J:225041
|
increased male germ cell apoptosis
|
J:225041
|
multinucleated giant male germ cells
|
J:225041
|
Scml2em2Shnk/Scml2em2Shnk
(C57BL/6J-Scml2em2Shnk)
|
azoospermia
|
J:225041
|
increased male germ cell apoptosis
|
J:225041
|
multinucleated giant male germ cells
|
J:225041
|
Scn8amed-J/Scn8amed-J Scnm1s/Scnm1s
(involves: C57BL/6J * STOCK Krt71Ca)
|
abnormal cell physiology
|
J:141236
|
Scn8amed-J/Scn8amed-J Scnm1tm1.1Mm/Scnm1tm1.1Mm
(involves: C57BL/6 * FVB * SJL * STOCK Krt71Ca)
|
abnormal cell physiology
|
J:141236
|
Scn8amed-jo2J/Scn8amed-jo2J
(B6(129S7)-Scn8amed-jo2J/J)
|
oligozoospermia
|
J:92160
|
Sco1tm1c(KOMP)Wtsi/Sco1tm1c(KOMP)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * C57BL/6N * DBA)
|
abnormal mitochondrial physiology
|
J:222036
|
increased mitochondrial number
|
J:222036
|
Sco2tm1.1Easc/Sco2tm2.1Easc
(129X1/SvJ-Sco2tm1.1Easc/Sco2tm2.1Easc)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:155116
|
Sco2tm2.1Easc/Sco2tm2.1Easc
(129X1/SvJ-Sco2tm2.1Easc)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:155116
|
Scube2tm1.1Rbya/Scube2tm1.1Rbya
(B6.129-Scube2tm1.1Rbya)
|
decreased chondrocyte proliferation
|
J:226676
|
Scyl2tm1.1Spel/Scyl2tm1.1Spel Tg(Nes-cre)1Kln/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased neuron apoptosis
|
J:225808
|
Scyl3tm1.1Spel/Scyl3tm1.1Spel
(involves: 129S6/SvEvTac * C57BL/6J)
|
cellular phenotype
|
J:262629
|
Sdc1tm1Cma/Sdc1tm1Cma
(either: C.Cg-Sdc1tm1Cma or B6.Cg-Sdc1tm1Cma)
|
abnormal cell proliferation
|
J:80682
|
Sdc2tm1c(KOMP)Wtsi/Sdc2tm1c(KOMP)Wtsi Tg(Pdgfb-icre/ERT2,-EGFP)1Frut/0
(involves: C57BL/6J * C57BL/6N * CBA)
|
decreased endothelial cell proliferation
|
J:276769
|
decreased vascular endothelial cell proliferation
|
J:276769
|
Sdc2tm1d(KOMP)Wtsi/Sdc2tm1d(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
decreased vascular endothelial cell proliferation
|
J:276769
|
Sdc4tm1Goe/Sdc4+
(involves: 129S4/SvJae * C57BL/6)
|
decreased fibroblast cell migration
|
J:67007
|
Sdc4tm1Goe/Sdc4tm1Goe
(involves: 129S4/SvJae * C57BL/6)
|
decreased fibroblast cell migration
|
J:67007
|
Sdc4tm1Tmu/Sdc4tm1Tmu
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal cell adhesion
|
J:60596
|
Sdccag8em1Lji/Sdccag8em1Lji
(involves: C57BL/6)
|
abnormal photoreceptor connecting cilium morphology
|
J:328191
|
abnormal primary cilium morphology
|
J:328191
|
absent kidney epithelial cell primary cilium
|
J:328191
|
increased retina apoptosis
|
J:328191
|
Sdccag8em2Lji/Sdccag8em2Lji
(involves: C57BL/6)
|
abnormal kidney epithelial cell primary cilium morphology
|
J:328191
|
abnormal photoreceptor connecting cilium morphology
|
J:328191
|
abnormal primary cilium morphology
|
J:328191
|
decreased kidney epithelial cell primary cilium length
|
J:328191
|
increased retina apoptosis
|
J:328191
|
Sdccag8Gt(OST40418)Lex/Sdccag8Gt(OST40418)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal DNA replication
|
J:226661
|
cellular phenotype
|
J:226661
|
Sdccag8tm1e(EUCOMM)Wtsi/Sdccag8tm1e(EUCOMM)Wtsi
(involves: C57BL/6)
|
abnormal neuronal migration
|
J:215665
|
abnormal nonmotile primary cilium morphology
|
J:215665
|
Sdhaf4em1Bcgen/Sdhaf4em1Bcgen Tg(Ckmm-cre)5Khn/0
(B6.Cg-Sdhaf4em1Bcgen Tg(Ckmm-cre)5Khn)
|
abnormal mitochondrial physiology
|
J:345348
|
abnormal myocardial fiber mitochondrial morphology
|
J:345348
|
abnormal tricarboxylic acid cycle
|
J:345348
|
decreased myocardial fiber mitochondrial DNA content
|
J:345348
|
Sdhbtm1c(EUCOMM)Hmgu/Sdhbtm1c(EUCOMM)Hmgu Tg(Ins2-cre)23Herr/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
abnormal cellular respiration
|
J:326592
|
abnormal respiratory electron transport chain
|
J:326592
|
Sdhctm1c(EUCOMM)Wtsi/Sdhctm1c(EUCOMM)Wtsi Gt(ROSA)26Sortm1.1(rtTA,tetO-cre)Bkmn/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N)
|
abnormal tricarboxylic acid cycle
|
J:284745
|
Sdhdtm1Jlob/Sdhd+
(involves: 129X1/SvJ)
|
abnormal respiratory electron transport chain
|
J:95252
|
Sdhdtm1Jlob/Sdhdtm2Jlob Thtm1(cre)Te/Th+
(involves: 129S1/Sv * 129X1/SvJ)
|
oxidative stress
|
J:186713
|
Sec23aGt(RRE297)Byg/Sec23aGt(RRE297)Byg
(B6J.129P2-Sec23aGt(RRE297)Byg)
|
increased amnion apoptosis
|
J:237614
|
increased endoplasmic reticulum stress
|
J:237614
|
Sec23bGt(AD0407)Wtsi/Sec23bGt(AD0407)Wtsi
(B6J.129P2-Sec23bGt(AD0407)Wtsi)
|
abnormal intestinal goblet cell morphology
|
J:186391
|
increased apoptosis
|
J:186391
|
Sec23iptm1.1Katn/Sec23iptm1.1Katn
(involves: C57BL/6 * CBA)
|
abnormal acrosome assembly
|
J:174226
|
abnormal sperm mitochondrial sheath morphology
|
J:174226
|
abnormal sperm nucleus morphology
|
J:174226
|
decreased elongated spermatid number
|
J:174226
|
globozoospermia
|
J:174226
|
Sec61a1m1Gek/Sec61a1m1Gek
(C57BL/6J-Sec61a1m1Gek)
|
increased hepatocyte apoptosis
|
J:164159
|
increased hepatocyte proliferation
|
J:164159
|
increased pancreatic beta cell apoptosis
|
J:164159
|
Seh1ltm1Lzha/Seh1ltm1Lzha Olig1tm1(cre)Rth/Olig1+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell differentiation
|
J:276253
|
Seh1ltm1Lzha/Seh1ltm1Lzha Tg(Cspg4-cre/Esr1*)BAkik/0
(involves: 129 * C57BL/6)
|
abnormal cell differentiation
|
J:276253
|
Sel1lGt(CA0017)Wtsi/Sel1lGt(CA0017)Wtsi
(involves: 129P2/OlaHsd)
|
abnormal pancreatic alpha cell differentiation
|
J:158780
|
abnormal pancreatic beta cell differentiation
|
J:158780
|
decreased hepatocyte proliferation
|
J:158780
|
increased endoplasmic reticulum stress
|
J:158780
|
Sel1ltm1c(KOMP)Wtsi/Sel1ltm1c(KOMP)Wtsi Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * C57BL/6N * CBA * SJL)
|
abnormal cell morphology
|
J:206568
|
abnormal endoplasmic reticulum morphology
|
J:206568
|
increased cell death
|
J:206568
|
increased pancreas apoptosis
|
J:206568
|
Seletm1Dmil/Seletm1Dmil
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal leukocyte adhesion
|
J:113169
|
Seletm1Hyn/Seletm1Hyn Selltm1Hyn/Selltm1Hyn Selptm1Hyn/Selptm1Hyn
(involves: 129S2/SvPas * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:57973
|
Seletm1Hyn/Seletm1Hyn Selptm1Hyn/Selptm1Hyn
(involves: 129S2/SvPas)
|
abnormal granulocyte differentiation
|
J:31626
|
impaired leukocyte tethering or rolling
|
J:31626
|
Seletm1Hyn/Seletm1Hyn Selptm1Hyn/Selptm1Hyn
(involves: 129S2/SvPas * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:57973
|
Seletm2Alb/Seletm2Alb Selltm2Alb/Selltm2Alb Selptm1Bay/Selptm1Bay
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cellular extravasation
|
J:70682
|
impaired leukocyte tethering or rolling
|
J:70682
|
Seletm2Alb/Seletm2Alb Selptm1Bay/Selptm1Bay
(involves: 129S7/SvEvBrd * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:70682
|
Seletm2Hyn/Seletm2Hyn
(involves: 129S2/SvPas * C57BL/6)
|
enhanced leukocyte tethering or rolling
|
J:57973
|
Selenoftm1Vgla/Selenoftm1Vgla
(involves: 129 * C57BL/6)
|
cellular phenotype
|
J:176744
|
oxidative stress
|
J:176744
|
Selenoktm1.2Itl/Selenoktm1.2Itl
(involves: BALB/cJ * C57BL/6)
|
decreased T cell proliferation
|
J:169169
|
impaired neutrophil chemotaxis
|
J:169169
|
Selenontm1Begg/Selenontm1Begg
(involves: C57BL/6 * C57BL/6NTac)
|
increased apoptosis
|
J:197753
|
Selenoptm1Rfb/Selenoptm1Rfb
(B6.129-Selenoptm1Rfb)
|
increased hepatocyte apoptosis
|
J:134536
|
Selenoptm2Rfb/Selenoptm2Rfb
(B6.Cg-Selenoptm2Rfb)
|
abnormal sperm flagellum morphology
|
J:121127
|
abnormal sperm midpiece morphology
|
J:121127
|
decreased sperm mitochondrial sheath size
|
J:121127
|
hairpin sperm flagellum
|
J:121127
|
Selenoptm3.1Rfb/Selenoptm3.1Rfb Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA)
|
oligozoospermia
|
J:192636
|
teratozoospermia
|
J:192636
|
Selenowem#Hwl/Selenowem#Hwl
(C57BL/6-Selenowem#Hwl)
|
abnormal osteoclast differentiation
|
J:317012
|
Selltm1Pest/Sell+
(involves: 129S4/SvJae * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:112550
|
Selltm1Pest/Selltm1Pest
(involves: 129S4/SvJae)
|
abnormal leukocyte adhesion
|
J:111233
|
impaired leukocyte tethering or rolling
|
J:111233
|
increased T cell proliferation
|
J:111233
|
Selltm1Pest/Selltm1Pest
(involves: 129S4/SvJae * C57BL/6)
|
abnormal leukocyte migration
|
J:112550
|
decreased T cell proliferation
|
J:112550
|
impaired leukocyte tethering or rolling
|
J:112550
|
Selltm1Tft/Selltm1Tft
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cellular extravasation
|
J:25005
|
abnormal leukocyte migration
|
J:25005
|
impaired leukocyte tethering or rolling
|
J:25005
|
Selltm1Tft/Selltm1Tft
(B6.129-Selltm1Tft)
|
abnormal cellular extravasation
|
J:66107
|
abnormal leukocyte migration
|
J:66107
|
Selltm1Tft/Selltm1Tft
(B6.129P2-Selltm1Tft)
|
abnormal cellular extravasation
|
J:48271
|
impaired leukocyte tethering or rolling
|
J:48271
|
Selltm2Hyn/Selltm2Hyn
(involves: 129S2/SvPas * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:57973
|
Selltm2Hyn/Selltm2Hyn
(involves: 129S2/SvPas * BALB/c)
|
impaired leukocyte tethering or rolling
|
J:114317
|
Selltm2Tft/Selltm2.1Tft
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:142184
|
impaired leukocyte tethering or rolling
|
J:142184
|
Selltm3Hyn/Selltm3Hyn Selptm1Hyn/Selptm1Hyn
(involves: 129S2/SvPas * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:57973
|
Selltm4Hyn/Selltm4Hyn Selptm1Hyn/Selptm1Hyn
(involves: 129S2/SvPas * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:57973
|
Selptm1.1Rpmc/Selptm1.1Rpmc
(B6.129S1-Selptm1.1Rpmc)
|
impaired leukocyte tethering or rolling
|
J:230041
|
Selptm1Bay/Selptm1Bay
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal leukocyte migration
|
J:24239
|
Selptm1Bay/Selptm1Bay
(either: B6.129S7-Selptm1Bay or (involves: 129S7/SvEvBrd * C57BL/6))
|
abnormal leukocyte tethering or rolling
|
J:31374
|
Selptm1Hyn/Selptm1Hyn
(involves: 129S2/SvPas * C57BL/6J)
|
impaired leukocyte tethering or rolling
|
J:77329
|
Selptm1Hyn/Selptm1Hyn
(involves: 129S2/SvPas)
|
impaired leukocyte tethering or rolling
|
J:29814
|
impaired macrophage chemotaxis
|
J:29814
|
Selptm1Hyn/Selptm1Hyn
(involves: 129S2/SvPas * C57BL/6)
|
impaired leukocyte tethering or rolling
|
J:57973
|
Selptm2Hyn/Selptm2Hyn
(involves: 129S2/SvPas * C57BL/6J)
|
impaired leukocyte tethering or rolling
|
J:51068
|
Selplgtm1Fur/Selplgtm1Fur
(involves: 129/Sv * C57BL/6J * SJL)
|
impaired leukocyte tethering or rolling
|
J:75412
|
impaired neutrophil chemotaxis
|
J:75412
|
Selplgtm1Rpmc/Selplgtm1Rpmc
(involves: 129S1/Sv * C57BL/6J)
|
abnormal leukocyte adhesion
|
J:75829
|
impaired leukocyte tethering or rolling
|
J:75829,
J:138731
|
Selplgtm2Rpmc/Selplgtm2Rpmc
(B6.Cg-Selplgtm2Rpmc)
|
impaired leukocyte tethering or rolling
|
J:138731
|
Sema3am808Ddg/Sema3am808Ddg
(involves: C3H/He * C57BL/6)
|
abnormal axon fasciculation
|
J:159834
|
Sema3am808Ddg/Sema3atm1Mcf
(involves: 129S4/SvJae * C3H/He * C57BL/6)
|
abnormal axon fasciculation
|
J:159834
|
Sema3atm1.1Tyag/Sema3atm1.1Tyag Vegfatm1Pec/Vegfatm1Pec
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal neuronal migration
|
J:175836
|
Sema3atm1Mcf/Sema3a+
(involves: 129S4/SvJae)
|
abnormal neuron differentiation
|
J:127639
|
Sema3atm1Mcf/Sema3atm1Mcf
(involves: 129S4/SvJae)
|
abnormal neuron differentiation
|
J:127639
|
Sema3ctm1.1Jra/Sema3ctm1.1Jra
(involves: 129P2/OlaHsd * CD-1)
|
abnormal neural crest cell migration
|
J:71240
|
Sema3ftm1.1Ddg/Sema3ftm1.1Ddg Tg(Syn1-cre)671Jxm/0
(involves: C57BL/6 * CBA)
|
abnormal axon fasciculation
|
J:84687
|
Sema3ftm1.1Ddg/Sema3ftm1.2Ddg Tg(Syn1-cre)671Jxm/0
(involves: C57BL/6 * CBA)
|
abnormal axon fasciculation
|
J:84687
|
Sema3ftm1.2Ddg/Sema3ftm1.2Ddg
(Not Specified)
|
abnormal axon fasciculation
|
J:84687
|
abnormal axon guidance
|
J:84687
|
Sema3ftm1Atai/Sema3ftm1Atai
(involves: 129P2/OlaHsd * C57BL/6J * ICR)
|
abnormal neuronal migration
|
J:134616
|
Sema4atm1Kik/Sema4atm1Kik
(Not Specified)
|
increased retina apoptosis
|
J:119485
|
Sema4atm3.1Akum/Sema4atm3.1Akum
(involves: C57BL/6J)
|
increased retina apoptosis
|
J:205754
|
Sema4ctm1Matl/Sema4ctm1Matl
(B6.129P2-Sema4ctm1Matl)
|
abnormal cerebellar granule cell migration
|
J:167973
|
Sema4dtm1Kik/Sema4dtm1Kik
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:66033
|
Sema7atm1Alk/Sema7atm1Alk
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal axon extension
|
J:87191
|
Semg1tm1Kemi/Semg1tm1Kemi Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
(involves: 129 * C57BL/6 * C57BL/6N * DBA/2)
|
abnormal sperm motility
|
J:207389
|
Semg1tm2Kemi/Semg1tm2Kemi Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
(involves: 129 * C57BL/6 * C57BL/6N * DBA/2)
|
abnormal sperm motility
|
J:207389
|
Senp1m1Mku/Senp1m1Mku
(involves: 129)
|
abnormal cell death
|
J:99175
|
Senp1tm1.1Wami/Senp1tm1.1Wami
(involves: 129 * C57BL/6)
|
abnormal granulocyte differentiation
|
J:163428
|
abnormal monocyte differentiation
|
J:163428
|
Senp1tm1Wami/Senp1tm1Wami Tg(Adipoq-cre)1Evdr/0
(B6.Cg-Senp1tm1Wami Tg(Adipoq-cre)1Evdr)
|
increased pancreatic beta cell apoptosis
|
J:228009
|
Senp1tm1Wami/Senp1tm1Wami Tg(Pdgfra-cre)1Clc/0
(B6.Cg-Senp1tm1Wami Tg(Pdgfra-cre)1Clc)
|
abnormal pancreatic islet cell apoptosis
|
J:228009
|
Septin4tm1Hs/Septin4+
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6J)
|
kinked sperm flagellum
|
J:96669
|
Septin4tm1Hs/Septin4tm1Hs
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6J)
|
abnormal sperm fibrous sheath morphology
|
J:96669
|
abnormal sperm mitochondrial morphology
|
J:96669
|
abnormal sperm principal piece morphology
|
J:96669
|
absent sperm annulus
|
J:96669
|
hairpin sperm flagellum
|
J:96669
|
immotile sperm
|
J:96669
|
teratozoospermia
|
J:96669
|
thin sperm flagellum
|
J:96669
|
Septin4tm1Ksh/Septin4tm1Ksh
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal sperm fibrous sheath morphology
|
J:96670
|
absent sperm annulus
|
J:96670
|
asthenozoospermia
|
J:96670
|
kinked sperm flagellum
|
J:96670
|
Septin7tm1Mgl/Septin7tm1Mgl
(involves: 129P2/OlaHsd * C3H * C57BL/6)
|
abnormal cell cycle
|
J:223786
|
abnormal mitotic cytokinesis
|
J:223786
|
cellular phenotype
|
J:223786
|
decreased fibroblast proliferation
|
J:223786
|
increased cell mass
|
J:223786
|
increased cell nucleus count
|
J:223786
|
Septin9tm1Emfu/Septin9tm1Emfu
(Not Specified)
|
increased apoptosis
|
J:205180
|
Septin9tm1Emfu/Septin9tm2.2Emfu
(Not Specified)
|
increased apoptosis
|
J:205180
|
Septin9tm2.1Emfu/Septin9tm2.1Emfu Tg(Lck-cre)548Jxm/0
(involves: C57BL/6 * CBA)
|
decreased T cell proliferation
|
J:205027
|
Septin9tm2.2Emfu/Septin9tm2.2Emfu
(Not Specified)
|
increased apoptosis
|
J:205180
|
Septin12em1Lych/Septin12em1Lych
(C57BL/6-Septin12em1Lych)
|
abnormal acrosome assembly
|
J:324492
|
abnormal sperm connecting piece morphology
|
J:324492
|
abnormal spermatid morphology
|
J:324492
|
absent sperm head
|
J:324492
|
asthenozoospermia
|
J:324492
|
globozoospermia
|
J:324492
|
kinked sperm flagellum
|
J:324492
|
oligozoospermia
|
J:324492
|
teratozoospermia
|
J:324492
|
Septin12tm1.1Plk/Septin12+
(chimera involves: 129/Sv * C57BL/6)
|
abnormal acrosome morphology
|
J:147965
|
abnormal male germ cell apoptosis
|
J:147965
|
abnormal sperm head morphology
|
J:147965
|
abnormal sperm nucleus morphology
|
J:147965
|
absent sperm flagellum
|
J:147965
|
asthenozoospermia
|
J:147965
|
decreased male germ cell number
|
J:147965
|
detached acrosome
|
J:147965
|
globozoospermia
|
J:147965
|
kinked sperm flagellum
|
J:147965
|
oligozoospermia
|
J:147965
|
Septin12tm3Plk/Septin12+
(involves: 129 * C57BL/6)
|
asthenozoospermia
|
J:223228
|
Septin12tm3Plk/Septin12tm3Plk
(involves: 129 * C57BL/6)
|
abnormal sperm annulus morphology
|
J:223228
|
abnormal sperm flagellum morphology
|
J:223228
|
asthenozoospermia
|
J:223228
|
kinked sperm flagellum
|
J:223228
|
Serac1em1Bcgen/Serac1em1Bcgen
(C57BL/6N-Serac1em1Bcgen)
|
abnormal cellular respiration
|
J:326672
|
abnormal mitochondrial fission
|
J:326672
|
abnormal oxidative phosphorylation
|
J:326672
|
decreased hepatocyte mitochondrial DNA content
|
J:326672
|
decreased mitochondrial DNA content
|
J:326672
|
decreased mitochondrial size
|
J:326672
|
decreased skeletal muscle fiber mitochondrial DNA content
|
J:326672
|
increased mitochondrial number
|
J:326672
|
Serpina3cem1Smoc/Serpina3cem1Smoc
(C57BL/6-Serpina3cem1Smoc)
|
decreased adipocyte glucose uptake
|
J:343846
|
increased white adipose tissue apoptosis
|
J:343846
|
Serpina3gtm1.1Arp/Serpina3gtm1.1Arp
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:189782
|
Serpina3gtm1.1Arp/Serpina3gtm1.1Arp Tg(TcrLCMV)#Sdz/0
(involves: C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:189782
|
Serpina3kem1(IMPC)J/Serpina3kem1(IMPC)J
(C57BL/6NJ-Serpina3kem1(IMPC)J/Mmjax)
|
abnormal redox activity
|
J:345330
|
decreased apoptosis
|
J:345330
|
Serpina5tm1Gei/Serpina5tm1Gei
(involves: 129/Sv * Swiss)
|
asthenozoospermia
|
J:66422
|
teratozoospermia
|
J:66422
|
Serpinb1atm1.1Cben/Serpinb1atm1.1Cben
(129S6/SvEvTac-Serpinb1atm1.1Cben)
|
impaired neutrophil chemotaxis
|
J:125918
|
Serpinb1atm1.1Cben/Serpinb1atm1.1Cben
(involves: 129S6/SvEvTac)
|
increased apoptosis
|
J:217636
|
Serpinb5tm1Zha/Serpinb5+
(involves: 129)
|
abnormal cell adhesion
|
J:89192
|
decreased cell proliferation
|
J:89192
|
Serpinb5tm1Zha/Serpinb5tm1Zha
(involves: 129)
|
absent inner cell mass proliferation
|
J:89192
|
decreased cell proliferation
|
J:89192
|
decreased inner cell mass proliferation
|
J:89192
|
Serpinb9tm1.1Pib/Serpinb9tm1.1Pib
(involves: BALB/cJ * C57BL/6J)
|
decreased cytotoxic T cell apoptosis
|
J:252016
|
Serpinb9tm1Arp/Serpinb9tm1Arp
(involves: C57BL/6)
|
increased apoptosis
|
J:113349
|
Serpine2tm1Dmn/Serpine2tm1Dmn
(B6.129P2-Serpine2tm1Dmn)
|
increased cell proliferation
|
J:121263
|
Serpine2tm1Dmn/Serpine2tm1Dmn Tg(Thy1-Serpine2)2Dmn/?
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased Schwann cell proliferation
|
J:121223
|
Sertad1tm1Srn/Sertad1tm1Srn
(involves: 129S1/Sv * 129X1/SvJ * BALB/c)
|
cellular phenotype
|
J:157231
|
Sertad2Gt(OST98734)Lex/Sertad2Gt(OST98734)Lex
(involves: 129S5/SvEvBrd)
|
decreased fibroblast proliferation
|
J:196054
|
Sesn1tm1a(EUCOMM)Wtsi/Sesn1tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
increased T cell proliferation
|
J:240602
|
Sesn2Gt(RRJ141)Byg/Sesn2Gt(RRJ141)Byg
(involves: 129P2/OlaHsd)
|
abnormal autophagy
|
J:189021
|
decreased adipocyte glucose uptake
|
J:189021
|
decreased hepatocyte mitochondrial DNA content
|
J:189021
|
decreased mitochondrial number
|
J:189021
|
Sesn2Gt(W077E06)Wrst/Sesn2Gt(W077E06)Wrst
(B6.129S2-Sesn2Gt(W077E06)Wrst)
|
decreased lung fibroblast proliferation
|
J:160854
|
increased cellular sensitivity to hydrogen peroxide
|
J:160854
|
increased fibroblast apoptosis
|
J:160854
|
Setd1aem1Yzhg/Setd1a+
(B6.Cg-Setd1aem1Yzhg)
|
abnormal synaptic vesicle exocytosis
|
J:328716
|
Setd1atm1Afst/Setd1atm1Afst
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:208420
|
abnormal DNA methylation
|
J:208420
|
cellular phenotype
|
J:208420
|
Setd1btm1.1Afst/Setd1btm1.1Afst
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
cellular phenotype
|
J:208420
|
Setd3tm1.1(NCOM)Mfgc/Setd3tm1.1(NCOM)Mfgc
(C57BL/6N-Setd3tm1.1(NCOM)Mfgc/Tcp)
|
abnormal DNA methylation
|
J:270048
|
decreased cell migration
|
J:270048
|
Setd4tm1c(KOMP)Wtsi/Setd4tm1c(KOMP)Wtsi Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C57BL/6 * C57BL/6N)
|
decreased apoptosis
|
J:297725
|
Setd5tm1.1Mgn/Setd5tm1.1Mgn
(involves: 129S6/SvEvTac * CD-1)
|
increased embryonic tissue cell apoptosis
|
J:237500
|
Setd7tm1.1Ital/Setd7tm1.1Ital
(involves: C57BL/6 * CBA)
|
abnormal extracellular matrix morphology
|
J:238299
|
Setd7tm1Frga/Setd7+
(involves: 129 * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:136558
|
decreased sensitivity to induced cell death
|
J:136558
|
Setd7tm1Frga/Setd7tm1Frga
(involves: 129 * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:136558
|
decreased sensitivity to induced cell death
|
J:136558
|
Setdb1tm1.1Yshk/Setdb1tm1.1Yshk Emx2tm2(cre)Sia/Emx2+
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal neuron differentiation
|
J:188109
|
abnormal neuronal precursor proliferation
|
J:188109
|
increased neuron apoptosis
|
J:188109
|
Setdb1tm1Enl/Setdb1tm1Enl
(involves: 129S4/SvJae)
|
decreased inner cell mass proliferation
|
J:89058
|
Setdb1tm2.1Enl/Setdb1tm2.2Enl
(involves: 129/Sv * C57BL/6)
|
abnormal cell morphology
|
J:161089
|
decreased cell proliferation
|
J:161089
|
Setxtm1.1Als/Setx+
(involves: 129 * C57BL/6J)
|
increased susceptibility to neuronal excitotoxicity
|
J:320844
|
Setxtm1.1Mfl/Setxtm1.1Mfl
(Not Specified)
|
abnormal double-strand DNA break repair
|
J:223053
|
abnormal male meiosis
|
J:223053
|
arrest of male meiosis
|
J:223053
|
azoospermia
|
J:223053
|
globozoospermia
|
J:223053
|
increased male germ cell apoptosis
|
J:223053
|
Sf3b4em1Mce/Sf3b4+
(C57BL/6J-Sf3b4em1Mce)
|
decreased neuronal precursor proliferation
|
J:285287
|
SfnEr/SfnEr
(B6CBACa Aw-J/A-SfnEr/J)
|
abnormal keratinocyte differentiation
|
J:102931
|
Sfntm1Mak/Sfntm1Mak
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell apoptosis
|
J:168328
|
increased B cell proliferation
|
J:168328
|
Sfntm1Mul/Sfntm1Mul Tg(MMTV-cre)7Mul/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal cell adhesion
|
J:159517
|
increased cell proliferation
|
J:159517
|
Sfpqtm1.1Takea/Sfpqtm1.1Takea Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * CBA/JNCrlj * SJL)
|
increased neuron apoptosis
|
J:271630
|
Sfrp2tm1Ktas/Sfrp2tm1Ktas
(involves: 129X1/SvJ)
|
abnormal interdigital cell death
|
J:138805
|
Sfrp2tm1Ktas/Sfrp2tm1Ktas
(involves: 129X1/SvJ * CBA/N)
|
abnormal interdigital cell death
|
J:138805
|
Sfrp2tm1Ktas/Sfrp2tm1Ktas
(involves: 129X1/SvJ * C57BL/6)
|
abnormal interdigital cell death
|
J:138805
|
Sfrp2tm1Sato/Sfrp2tm1Sato
(Not Specified)
|
abnormal neuron differentiation
|
J:112802
|
Sfxn3tm1b(KOMP)Wtsi/Sfxn3tm1b(KOMP)Wtsi
(C57BL/6N-Sfxn3tm1b(KOMP)Wtsi)
|
cellular phenotype
|
J:240628
|
Sgcetm1Ygl/Sgcetm1Ygl
(involves: 129S2/SvPas * 129S4/SvJaeSor * BALB/c * C57BL/6)
|
maternal imprinting
|
J:101332
|
Sgk3tm1Okad/Sgk3tm1Okad
(involves: 129P2/OlaHsd)
|
increased hair follicle apoptosis
|
J:100992
|
Sgms1Gt(E201D11)Wrst/Sgms1Gt(E201D11)Wrst
(B6.129P2-Sgms1Gt(E201D11)Wrst)
|
abnormal spermatid morphology
|
J:249941
|
absent acrosome
|
J:249941
|
absent sperm flagellum
|
J:249941
|
decreased male germ cell number
|
J:249941
|
increased testis apoptosis
|
J:249941
|
Sgms1tm1Kenw/Sgms1tm1Kenw
(involves: 129S2/SvPas * C57BL/6)
|
oxidative stress
|
J:168726
|
Sgms2tm1Jia/Sgms2tm1Jia
(involves: 129 * C57BL/6)
|
abnormal cell physiology
|
J:162192
|
Sgms2tm1Kenw/Sgms2tm1Kenw
(B6.129S2-Sgms2tm1Kenw)
|
abnormal cell physiology
|
J:175924
|
Sgo1Gt(neo-btk)1Dai/Sgo1+
(involves: 129S4/SvJae * C57BL/6)
|
aneuploidy
|
J:204809
|
chromosomal instability
|
J:204809
|
increased sensitivity to induced cell death
|
J:204809
|
polyploidy
|
J:204809
|
Sgo2aGt(D025B05)Wrst/Sgo2aGt(D025B05)Wrst
(involves: 129S2/SvPas * C57BL/6)
|
abnormal female meiosis
|
J:138779
|
arrest of male meiosis
|
J:138779
|
cellular phenotype
|
J:138779
|
decreased elongated spermatid number
|
J:138779
|
oligozoospermia
|
J:138779
|
Sgpl1Gt(ROSA)78Sor/Sgpl1Gt(ROSA)78Sor
(involves: 129S4/SvJaeSor)
|
abnormal cell migration
|
J:117491
|
decreased fibroblast cell migration
|
J:117491
|
Sgpl1Gt(ROSA)78Sor/Sgpl1Gt(ROSA)78Sor
(either: (involves: 129S4/SvJaeSor) or (involves: 129S4/SvJaeSor * C57BL/6))
|
abnormal spermatocyte morphology
|
J:142042
|
decreased spermatid number
|
J:142042
|
multinucleated giant male germ cells
|
J:142042
|
Sgpl1Gt(ROSA)78Sor/Sgpl1Gt(ROSA)78Sor
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal leukocyte migration
|
J:187619
|
Sgpp1tm1(KOMP)Vlcg/Sgpp1tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
abnormal keratinocyte differentiation
|
J:199597
|
increased keratinocyte proliferation
|
J:199597
|
Sgpp2tm1Rlp/Sgpp2tm1Rlp
(B6.129S6-Sgpp2tm1Rlp)
|
decreased pancreatic beta cell proliferation
|
J:235035
|
increased endoplasmic reticulum stress
|
J:235035
|
Sgshmps3a/Sgshmps3a
(involves: 129X1/SvJ * CD-1 * C57BL/6 * SJL)
|
abnormal cell morphology
|
J:72142
|
abnormal lysosome morphology
|
J:72142
|
Sh1SEG/Pas/Sh1SEG/Pas
(involves: C57BL/6J * SEG/Pas)
|
teratozoospermia
|
J:124156
|
Sh2SEG/Pas/Sh2SEG/Pas
(involves: C57BL/6J * SEG/Pas)
|
teratozoospermia
|
J:124156
|
Sh2b1tm1Ayos/Sh2b1tm1Ayos
(involves: C57BL/6)
|
abnormal oocyte morphology
|
J:78931
|
asthenozoospermia
|
J:78931
|
oligozoospermia
|
J:78931
|
Sh2b1tm2.1Lr/Sh2b1tm2.1Lr Tg(Pdx1-cre)89.1Dam/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * SJL)
|
increased pancreatic beta cell proliferation
|
J:209019
|
Sh2b3tm1Paw/Sh2b3tm1Paw
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal granulocyte differentiation
|
J:77248
|
abnormal monocyte differentiation
|
J:77248
|
increased cell proliferation
|
J:77248
|
Sh2d1atm1Cpt/Y
(involves: 129S4/SvJae * C57BL/6)
|
increased T cell proliferation
|
J:97756
|
Sh2d1atm1Cpt/Sh2d1a+
(involves: 129S4/SvJae * C57BL/6)
|
increased T cell proliferation
|
J:97756
|
Sh2d1atm1Cpt/Sh2d1atm1Cpt
(involves: 129S4/SvJae * C57BL/6)
|
increased T cell proliferation
|
J:97756
|
Sh2d1atm1Pls/Sh2d1atm1Pls
(either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6))
|
increased T cell proliferation
|
J:70032
|
Sh2d2atm1Jbs/Sh2d2atm1Jbs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased T cell proliferation
|
J:64938
|
Sh2d3ctm1.1Ebp/Sh2d3ctm1.1Ebp
(involves: C57BL/6)
|
abnormal axon extension
|
J:164874
|
Sh2d3ctm1Lex/Sh2d3ctm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal leukocyte migration
|
J:161448
|
Sh3SEG/Pas/Sh3SEG/Pas
(involves: C57BL/6J * SEG/Pas)
|
teratozoospermia
|
J:124156
|
Sh3bp2tm1Bjro/Sh3bp2+
(involves: 129S4/SvJae * BALB/cJ * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:117880
|
Sh3bp2tm1Bjro/Sh3bp2tm1Bjro
(involves: 129S4/SvJae * BALB/cJ * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:117880
|
Sh3bp2tm1Bjro/Sh3bp2tm1Bjro Tnftm1Gkl/Tnftm1Gkl
(involves: 129S/SvEv * 129S4/SvJae * BALB/cJ * C57BL/6J)
|
abnormal osteoclast differentiation
|
J:117880
|
Sh3bp2tm1Geha/Sh3bp2tm1Geha
(Not Specified)
|
decreased B cell proliferation
|
J:110319
|
Sh3bp2tm1Rtpl/Sh3bp2tm1Rtpl
(B6.129P2-Sh3bp2tm1Rtpl)
|
decreased B cell proliferation
|
J:121380
|
increased B cell apoptosis
|
J:121380
|
Sh3bp2tm1Rtpl/Sh3bp2tm1Rtpl
(involves: 129P2/OlaHsd * C57BL/6)
|
impaired macrophage phagocytosis
|
J:221901
|
Sh3glb1tm1Hgw/Sh3glb1tm1Hgw
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased fibroblast apoptosis
|
J:102178
|
Sh3glb2Gt(OST224737)Lex/Sh3glb2Gt(OST224737)Lex
(B6.129S5-Sh3glb2Gt(OST224737)Lex)
|
abnormal endocytosis
|
J:246421
|
cellular phenotype
|
J:246421
|
impaired autophagy
|
J:246421
|
Sh3yl1tm1Syb/Sh3yl1tm1Syb
(involves: C57BL/6N)
|
cellular phenotype
|
J:298830
|
decreased kidney apoptosis
|
J:298830
|
decreased renal tubule apoptosis
|
J:298830
|
Sh4SEG/Pas/Sh4SEG/Pas
(involves: C57BL/6J * SEG/Pas)
|
teratozoospermia
|
J:124156
|
Shali1129X1/SvJ/Shali1129X1/SvJ
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:127224
|
Shali1129X1/SvJ/Shali1129X1/SvJ Shali2C57BL/6J/Shali2C57BL/6J
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:127224
|
Shali2C57BL/6J/Shali2C57BL/6J
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:127224
|
Shali4C57BL/6J/Shali4C57BL/6J
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:127224
|
Shali5C57BL/6J/Shali5C57BL/6J
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:127224
|
Sharpincpdm/Sharpincpdm
(C57BL/KaLawRij-Sharpincpdm)
|
increased keratinocyte apoptosis
|
J:31745,
J:14539,
J:53575
|
increased keratinocyte proliferation
|
J:31745
|
Shc1tm1Paw/Shc1tm1Paw
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * CD-1))
|
abnormal actin cytoskeleton morphology
|
J:62182
|
abnormal cell adhesion
|
J:62182
|
abnormal cell morphology
|
J:62182
|
abnormal cell physiology
|
J:62182
|
Shc1tm1Pgp/Shc1tm1Pgp
(involves: 129)
|
decreased cellular sensitivity to hydrogen peroxide
|
J:81977,
J:58535
|
decreased cellular sensitivity to oxidative stress
|
J:58535
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:81977,
J:58535
|
oxidative stress
|
J:81977
|
Shcbp1ltm1a(KOMP)Wtsi/Shcbp1ltm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal meiotic spindle morphology
|
J:228105
|
arrest of male meiosis
|
J:228105
|
increased male germ cell apoptosis
|
J:228105
|
oligozoospermia
|
J:228105
|
ShhDsh/Shh+
(B10Rl.Cg-ShhDsh)
|
decreased chondrocyte proliferation
|
J:97323
|
Shhtm1Amc/Shhtm1Amc
(involves: 129/Sv * C57BL/6J * CBA/J)
|
decreased keratinocyte proliferation
|
J:50051
|
Shhtm1Chg/Shhtm1Chg
(involves: 129S1/Sv * 129X1/SvJ)
|
increased apoptosis
|
J:145182
|
Shhtm1Chg/Shhtm2Amc Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ)
|
abnormal neural crest cell apoptosis
|
J:135134
|
abnormal neural crest cell migration
|
J:135134
|
Shhtm3(cre)Chg/Shhtm3(cre)Chg
(Not Specified)
|
abnormal cell physiology
|
J:160335
|
Shmt2em1Jiha/Shmt2em1Jiha
(involves: C57BL/6JJcl)
|
abnormal respiratory electron transport chain
|
J:259713
|
decreased fibroblast proliferation
|
J:259713
|
Shoc1tm2Rjpz/Shoc1tm2Rjpz
(involves: C57BL/6N)
|
abnormal chiasmata formation
|
J:262079
|
abnormal chromosomal synapsis
|
J:262079
|
arrest of male meiosis
|
J:262079
|
azoospermia
|
J:262079
|
increased male germ cell apoptosis
|
J:262079
|
Shroom3Gt(ROSA53)Sor/Shroom3Gt(ROSA53)Sor
(B6.129S4-Shroom3Gt(ROSA53)Sor/J)
|
abnormal fibroblast physiology
|
J:293794
|
increased fetal cardiomyocyte proliferation
|
J:293794
|
Shtn1tm1Nngk/Shtn1tm1Nngk
(B6.129-Shtn1tm1Nngk)
|
abnormal axon fasciculation
|
J:272349
|
Siah1atm1Ddlb/Siah1atm1Ddlb
(involves: 129S1/Sv * C57BL/6J)
|
arrest of male meiosis
|
J:75489
|
azoospermia
|
J:75489
|
Siah1atm1Ddlb/Siah1atm1Ddlb
(involves: 129S1/Sv)
|
cellular phenotype
|
J:126183
|
Siah1atm1Ddlb/Siah1atm1Ddlb Siah2tm1Ddlb/Siah2tm1Ddlb
(involves: 129S1/Sv * 129S4/SvJae)
|
cellular phenotype
|
J:126183
|
Siah1btm1Ddlb/Y
(involves: C57BL/6J)
|
cellular phenotype
|
J:126183
|
Siah2tm1Ddlb/Siah2tm1Ddlb
(involves: 129S4/SvJae)
|
cellular phenotype
|
J:126183
|
Sidt2tm1.1Hzha/Sidt2tm1.1Hzha
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal endoplasmic reticulum morphology
|
J:236042
|
increased endoplasmic reticulum stress
|
J:236042
|
Sigirrtm1Lix/Sigirrtm1Lix
(involves: 129S6/SvEvTac * BALB/c)
|
abnormal splenocyte proliferation
|
J:85151
|
Siglec1tm1Croc/Siglec1tm1Croc
(B6.129-Siglec1tm1Croc)
|
impaired macrophage phagocytosis
|
J:189854
|
Siglec1tm2.1Croc/Siglec1tm2.1Croc
(B6.129P2(C)-Siglec1tm2.1Croc)
|
impaired macrophage phagocytosis
|
J:189854
|
Siglec15tm1Yohi/Siglec15tm1Yohi
(B6.129S6-Siglec15tm1Yohi)
|
abnormal osteoblast physiology
|
J:193852
|
abnormal osteoclast differentiation
|
J:193852
|
Siglecftm1.2Avrk/Siglecftm1.2Avrk
(B6.129(FVB)-Siglecftm1.2Avrk)
|
abnormal eosinophil differentiation
|
J:204811
|
Siglechtm1.1Cfg/Siglechtm1.1Cfg
(involves: C57BL/6)
|
increased T cell proliferation
|
J:217719
|
Sik2tm1Lex/Sik2tm1Lex
(involves: 129S/SvEvBrd)
|
abnormal fat cell differentiation
|
J:229999
|
decreased adipocyte glucose uptake
|
J:229999
|
decreased fatty acid oxidation
|
J:229999
|
decreased muscle cell glucose uptake
|
J:229999
|
Sik3tm1Htake/Sik3tm1Htake
(involves: C57BL/6JJcl * C57BL/6N)
|
abnormal fat cell differentiation
|
J:183827
|
Silc1em1Uli/Silc1em1Uli
(involves: C57BL/6)
|
abnormal axon extension
|
J:268832
|
Sim1tm1Jlmd/Sim1tm1Jlmd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal neuronal migration
|
J:120909
|
decreased apoptosis
|
J:120909
|
Sin3btm1.2Rdp/Sin3btm1.2Rdp
(involves: 129 * C57BL/6 * FVB/N * SJL)
|
abnormal cell cycle checkpoint function
|
J:154855
|
abnormal granulocyte differentiation
|
J:154855
|
Sirt1tm1.1Cxd/Sirt1tm1.1Cxd
(either: (involves: 129S6/SvEvTac * Black Swiss * FVB/N) or (involves: 129S6/SvEvTac * C57BL/6 * FVB/N))
|
abnormal cell cycle checkpoint function
|
J:140089
|
abnormal cell death
|
J:140089
|
abnormal chromosome morphology
|
J:140089
|
abnormal DNA repair
|
J:140089
|
abnormal DNA replication
|
J:140089
|
aneuploidy
|
J:140089
|
increased cellular sensitivity to gamma-irradiation
|
J:140089
|
increased cellular sensitivity to ultraviolet irradiation
|
J:140089
|
increased mitotic index
|
J:140089
|
Sirt1tm1Fwa/Sirt1tm1Fwa
(involves: 129/Sv * 129S6/SvEvTac)
|
increased cellular sensitivity to ionizing radiation
|
J:85542
|
oligozoospermia
|
J:85542
|
Sirt1tm1Mcby/Sirt1tm1Mcby
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal cellular respiration
|
J:133127
|
abnormal sperm flagellum morphology
|
J:81010
|
abnormal spermatid morphology
|
J:81010
|
globozoospermia
|
J:81010
|
immotile sperm
|
J:81010
|
increased male germ cell apoptosis
|
J:81010
|
oligozoospermia
|
J:81010
|
teratozoospermia
|
J:81010
|
Sirt1tm1Mcby/Sirt1tm1Mcby
(129/Sv-Sirt1tm1Mcby)
|
abnormal spermatocyte morphology
|
J:146009
|
arrest of male meiosis
|
J:146009
|
decreased spermatid number
|
J:146009
|
increased male germ cell apoptosis
|
J:146009
|
multinucleated giant male germ cells
|
J:146009
|
Sirt1tm2.1Mcby/Sirt1tm2.1Mcby
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
immotile sperm
|
J:180628
|
oligozoospermia
|
J:180628
|
Sirt2tm1.1Cxd/Sirt2tm1.1Cxd
(either: (involves: C57BL/6 * FVB/N) or (involves: FVB/N * NIH Black Swiss))
|
abnormal mitosis
|
J:177486
|
aneuploidy
|
J:177486
|
decreased fibroblast proliferation
|
J:177486
|
delayed cellular replicative senescence
|
J:177486
|
Sirt2tm1.1Fwa/Sirt2tm1.1Fwa
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal apoptosis
|
J:195041
|
abnormal cell cycle
|
J:195041
|
abnormal chromosome morphology
|
J:195041
|
abnormal mitosis
|
J:195041
|
Sirt3tm1.1Cxd/Sirt3tm1.1Cxd
(involves: 129S6/SvEvTac * Black Swiss * FVB/N)
|
abnormal cell physiology
|
J:142586
|
abnormal cellular respiration
|
J:142586
|
Sirt6tm1Fwa/Sirt6tm1Fwa
(involves: 129S6/SvEvTac * 129X1/SvJ)
|
decreased cell proliferation
|
J:112817
|
increased cellular sensitivity to alkylating agents
|
J:112817
|
increased cellular sensitivity to ionizing radiation
|
J:112817
|
spontaneous chromosome breakage
|
J:112817
|
Sirt6tm2.1Cxd/Sirt6tm2.1Cxd
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
early cellular replicative senescence
|
J:167023
|
Sirt6tm2.2Cxd/Sirt6tm2.2Cxd
(involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss)
|
early cellular replicative senescence
|
J:167023
|
Sirt7tm1Evbo/Sirt7tm1Evbo
(involves: 129/Sv * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:147652
|
increased cellular sensitivity to hydrogen peroxide
|
J:147652
|
increased sensitivity to induced cell death
|
J:147652
|
Sit1tm1Lsmn/Sit1tm1Lsmn
(B6.Cg-Sit1tm1Lsmn)
|
increased T cell proliferation
|
J:100408
|
Six1tm1Mair/Six1tm1Mair
(involves: 129S2/SvPas)
|
decreased otic epithelial cell proliferation
|
J:84417
|
Six1tm1Mair/Six1tm1Mair Six4tm1Mair/Six4tm1Mair
(either: 129/Sv-Six1tm1Mair Six4tm1Mair or B6N.129-Six1tm1Mair Six4tm1Mair)
|
abnormal muscle precursor cell migration
|
J:98519
|
Six1tm1Rsd/Six1tm1Rsd
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal muscle precursor cell migration
|
J:86619
|
decreased cell proliferation
|
J:86619
|
increased apoptosis
|
J:86619
|
Six1tm2Kwk/Six1tm2Kwk
(involves: 129P2/OlaHsd * C57BL/6)
|
increased neuron apoptosis
|
J:114468
|
Six5tm1Rdd/Six5+
(129S4/SvJae-Six5tm1Rdd)
|
oligozoospermia
|
J:91207
|
Six5tm1Rdd/Six5tm1Rdd
(129S4/SvJae-Six5tm1Rdd)
|
abnormal spermatid morphology
|
J:91207
|
azoospermia
|
J:91207
|
Skap1Gt713Lex/Skap1Gt713Lex
(B6.129S5-Skap1Gt713Lex)
|
decreased T cell proliferation
|
J:126545
|
Skap2Gt(VICTR20)21Lex/Skap2Gt(VICTR20)21Lex
(B6.129S5-Skap2Gt(VICTR20)21Lex)
|
decreased B cell proliferation
|
J:101373
|
skc6/skc6
(involves: C57BL/6J)
|
abnormal lysosome physiology
|
J:85113
|
skc9/skc9
(involves: C57BL/6J)
|
abnormal lysosome physiology
|
J:85113
|
skc10/skc10
(involves: C57BL/6J)
|
abnormal lysosome physiology
|
J:85113
|
skc12/skc12
(involves: C57BL/6J)
|
abnormal lysosome physiology
|
J:85113
|
skc30/skc30
(involves: C57BL/6J)
|
abnormal cell death
|
J:85113
|
skc31/skc31
(involves: C57BL/6J)
|
abnormal cell death
|
J:85113
|
skc37/skc37
(Not Specified)
|
abnormal lysosome morphology
|
J:89098
|
skc38/skc38
(Not Specified)
|
abnormal lysosome morphology
|
J:89098
|
Skitm1Cco/Ski+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased fibroblast proliferation
|
J:73349
|
Skitm1Cco/Skitm1Cco
(involves: 129P2/OlaHsd * Black Swiss)
|
increased fibroblast proliferation
|
J:73349
|
Skiltm1.1Kluo/Skiltm1.1Kluo
(B6.129P2-Skiltm1.1Kluo)
|
decreased fibroblast proliferation
|
J:154718
|
early cellular replicative senescence
|
J:154718
|
Skiltm1Spw/Skiltm1Spw
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
decreased T cell proliferation
|
J:84554
|
Skiltm2Spw/Skiltm2Spw
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
decreased T cell proliferation
|
J:84554
|
Skor2tm1Yono/Skor2tm1Yono
(involves: 129 * C57BL/6)
|
abnormal Purkinje cell differentiation
|
J:208769
|
abnormal Purkinje cell migration
|
J:208769
|
Skor2Tn(sb-Tyr)1799B.CA7BOve/Skor2Tn(sb-Tyr)1799B.CA7BOve
(involves: FVB/N)
|
abnormal Purkinje cell differentiation
|
J:178891
|
decreased cerebellar granule cell precursor proliferation
|
J:178891
|
Skor2Tn(sb-Tyr)1799B.CA7Ove/Skor2Tn(sb-Tyr)1799B.CA7Ove
(involves: FVB/N)
|
abnormal Purkinje cell differentiation
|
J:178818
|
decreased cerebellar granule cell precursor proliferation
|
J:178818
|
Skp1tm1.1Jw/Skp1tm1.2Jw Tg(Ddx4-cre)1Dcas/0
(involves: 129S4/SvJae * C57BL/6 * FVB)
|
absent germ cells
|
J:289957
|
Skp1tm1.1Jw/Skp1tm1.2Jw Tg(Ddx4-cre/ERT2)1Dcas/0
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal chromosomal synapsis
|
J:289957
|
abnormal double-strand DNA break repair
|
J:289957
|
abnormal female meiosis
|
J:289957
|
arrest of male meiosis
|
J:289957
|
azoospermia
|
J:289957
|
maternal effect
|
J:289957
|
oocyte degeneration
|
J:289957
|
Skp2tm1Kin/Skp2tm1Kin
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell proliferation
|
J:62130
|
increased fibroblast apoptosis
|
J:62130
|
Slatm1Weis/Slatm1Weis Sla2tm1Amch/Sla2tm1Amch
(involves: 129)
|
abnormal dendritic cell differentiation
|
J:169170
|
Slc1a1tm1Wst/Slc1a1tm1Wst
(B6.129-Slc1a1tm1Wst)
|
increased cellular sensitivity to hydrogen peroxide
|
J:124191
|
Slc1a2tm1Kta/Slc1a2+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:144898
|
Slc1a2tm1Kta/Slc1a2+ Tg(SOD1*G93A)1Gur/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * SJL/J)
|
abnormal cell physiology
|
J:144898
|
Slc1a3tm1Kta/Slc1a3tm1Kta
(B6.129P2-Slc1a3tm1Kta)
|
increased cellular sensitivity to hydrogen peroxide
|
J:124191
|
Slc2a1Rgsc200/Slc2a1+
(B6(D2)-Slc2a1Rgsc200)
|
decreased cellular glucose uptake
|
J:281292
|
Slc2a1tm1Dcdv/Slc2a1+
(involves: 129S6/SvEvTac * C57BL/6J)
|
decreased cellular glucose uptake
|
J:108250
|
Slc2a4tm1Abel/Slc2a4+ Tg(Ckmm-cre)5Khn/0
(involves: 129S4/SvJae * FVB)
|
decreased muscle cell glucose uptake
|
J:110773
|
Slc2a4tm1Abel/Slc2a4tm1Abel Tg(Ckmm-cre)5Khn/?
(involves: 129/Sv * C57BL/6)
|
decreased skeletal muscle cell glucose uptake
|
J:75418
|
Slc2a4tm1Abel/Slc2a4tm1Abel Tg(Ckmm-cre)5Khn/0
(involves: 129S4/SvJae * FVB)
|
decreased adipocyte glucose uptake
|
J:110773
|
decreased skeletal muscle cell glucose uptake
|
J:110773
|
increased adipocyte glucose uptake
|
J:110773
|
Slc2a4tm1Abel/Slc2a4tm1Abel Tg(Myhca-cre)1Abel/?
(involves: 129S4/SvJae * FVB)
|
decreased cardiac muscle cell glucose uptake
|
J:59054
|
Slc2a4tm1Abel/Slc2a4tm1Abel Tg(Myhca-cre)1Abel/?
(involves: 129S4/SvJae * C57BL/6 * FVB)
|
decreased cardiac muscle cell glucose uptake
|
J:108830
|
increased cardiac muscle cell glucose uptake
|
J:108830
|
Slc2a4tm1Jdz/Slc2a4tm1Jdz
(involves: 129S1/Sv * C57BL/6)
|
decreased adipocyte glucose uptake
|
J:123335
|
decreased skeletal muscle cell glucose uptake
|
J:123335
|
Slc2a4tm1Jdz/Slc2a4tm1Jdz Tg(ACTA1-cre)1Jdz/0
(involves: 129S1/Sv * C57BL/6 * CBA)
|
cardiac interstitial fibrosis
|
J:123335
|
decreased adipocyte glucose uptake
|
J:123335
|
decreased skeletal muscle cell glucose uptake
|
J:123335
|
increased adipocyte glucose uptake
|
J:123335
|
increased cardiac muscle cell glucose uptake
|
J:123335
|
increased skeletal muscle cell glucose uptake
|
J:123335
|
Slc2a4tm1Mch/Slc2a4+
(involves: 129/Sv * C57BL/6J * CD-1 * SJL)
|
decreased muscle cell glucose uptake
|
J:43935
|
decreased skeletal muscle cell glucose uptake
|
J:43650
|
Slc2a4tm1Mch/Slc2a4tm1Mch
(involves: 129/Sv * C57BL/6J * SJL)
|
cardiac interstitial fibrosis
|
J:107849
|
Slc2a8tm1.1Asch/Slc2a8tm1.1Asch
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
asthenozoospermia
|
J:159441
|
Slc3a2tm1.1Merl/Slc3a2+ Tg(Vil1-cre)997Gum/0
(B6.Cg-Slc3a2tm1.1Merl Tg(Vil1-cre)997Gum)
|
abnormal enterocyte proliferation
|
J:173946
|
Slc3a2tm1.1Mgin/Slc3a2tm1.1Mgin
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal cell morphology
|
J:134813
|
Slc3a2tm1.1Yait/Slc3a2tm1.1Yait Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd * C57BL/6NCrSlc)
|
abnormal macrophage differentiation
|
J:188365
|
impaired macrophage phagocytosis
|
J:188365
|
Slc4a1tm1Llp/Slc4a1tm1Llp
(B6;129S4-Slc4a1tm1Llp/J)
|
cardiac interstitial fibrosis
|
J:120610
|
Slc4a1wan/Slc4a1wan
(C3H/HeJ-Slc4a1wan/J)
|
binucleate
|
J:85322
|
Slc4a2tm1Jmed/Slc4a2tm1Jmed
(involves: 129P2/OlaHsd * FVB)
|
abnormal apoptosis
|
J:88196
|
azoospermia
|
J:88196
|
Slc4a3tm1Ges/Slc4a3tm1Ges
(involves: 129X1/SvJ)
|
increased retina apoptosis
|
J:129363
|
Slc4a7tm1Krtz/Slc4a7tm1Krtz
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal retina apoptosis
|
J:86635
|
Slc5a5tm1d(KOMP)Wtsi/Slc5a5tm1d(KOMP)Wtsi
(involves: C57BL/6 * FVB/N * SJL)
|
abnormal redox activity
|
J:250121
|
Slc6a3tm1.1Jaja/Slc6a3tm1.1Jaja
(B6.129-Slc6a3tm1.1Jaja)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:180517
|
Slc6a3tm4.1(tTA)Xz/Slc6a3+ Tg(tetO-SNCA*A53T)E2Cai/0
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6)
|
abnormal mitochondrial physiology
|
J:218892
|
abnormal mitochondrial shape
|
J:218892
|
decreased mitochondrial size
|
J:218892
|
Slc6a4tm2.1Rbl/Slc6a4tm2.1Rbl
(involves: 129S4/SvJae * 129S6/SvEvTac)
|
abnormal small intestinal crypt cell proliferation
|
J:237081
|
Slc6a8tm1.1Lbar/Y Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * C57BL/6J * C57BL/6N * SJL)
|
abnormal neuron proliferation
|
J:238578
|
Slc6a8tm1.2Lbar/Y
(involves: 129 * 129S1/Sv * C57BL/6J * C57BL/6N)
|
abnormal neuron proliferation
|
J:238578
|
Slc7a1tm1Rbmn/Slc7a1tm1Rbmn
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: C57BL/6))
|
abnormal cell physiology
|
J:39649
|
Slc7a5tm1.1Daca/Slc7a5tm1.1Daca Tg(Tek-cre)12Flv/0
(B6J.Cg-Slc7a5tm1.1Daca Tg(Tek-cre)12Flv)
|
abnormal translation
|
J:238065
|
Slc7a11m1Mtka/Slc7a11m1Mtka
(C57BL/6-Slc7a11m1Mtka)
|
decreased fibroblast proliferation
|
J:159323
|
Slc7a11tm1Hsat/Slc7a11tm1Hsat
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell death
|
J:102902
|
decreased fibroblast proliferation
|
J:102902
|
Slc8a1tm1Herc/Slc8a1+
(involves: 129 * CD-1)
|
increased pancreatic beta cell proliferation
|
J:186743
|
Slc8a1tm1Sjc/Slc8a1tm1Sjc
(involves: 129X1/SvJ * C57BL/6)
|
increased embryonic tissue cell apoptosis
|
J:69362
|
Slc8a1tm1Yin/Slc8a1+
(involves: 129X1/SvJ * C57BL/6J)
|
cardiac interstitial fibrosis
|
J:75050
|
Slc8a1tm1Yin/Slc8a1tm1Yin
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:102564
|
abnormal mitochondrial crista morphology
|
J:102564
|
abnormal mitochondrial matrix morphology
|
J:102564
|
abnormal mitochondrial shape
|
J:102564
|
dilated mitochondrion
|
J:102564
|
increased cardiomyocyte apoptosis
|
J:65985
|
Slc8b1tm1c(EUCOMM)Wtsi/Slc8b1tm1c(EUCOMM)Wtsi A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129S4/SvJaeSor * C57BL/6N * FVB/N)
|
dilated mitochondrion
|
J:325413
|
Slc9a8Gt(YHB273)Byg/Slc9a8Gt(YHB273)Byg
(involves: 129P2/OlaHsd * Black Swiss)
|
abnormal colon goblet cell morphology
|
J:191151
|
Slc9a8tm1c(KOMP)Wtsi/Slc9a8tm1c(KOMP)Wtsi Tg(Stra8-icre)1Reb/0
(involves: C57BL/6J * C57BL/6N * FVB/NJ)
|
abnormal acrosome assembly
|
J:245977
|
abnormal proacrosomal vesicle fusion
|
J:245977
|
abnormal sperm head morphology
|
J:245977
|
abnormal sperm mitochondrial sheath morphology
|
J:245977
|
absent acrosome
|
J:245977
|
absent sperm mitochondrial sheath
|
J:245977
|
globozoospermia
|
J:245977
|
Slc9a8tm1d(KOMP)Wtsi/Slc9a8tm1d(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal acrosome assembly
|
J:245977
|
abnormal proacrosomal vesicle fusion
|
J:245977
|
abnormal sperm mitochondrial sheath morphology
|
J:245977
|
abnormal sperm nucleus morphology
|
J:245977
|
absent acrosome
|
J:245977
|
absent sperm mitochondrial sheath
|
J:245977
|
asthenozoospermia
|
J:245977
|
globozoospermia
|
J:245977
|
Slc9a8tm1d(KOMP)Wtsi/Slc9a8tm1d(KOMP)Wtsi Tg(CAG-RFP,Acr-EGFP)RBGS002Osb/0
(involves: C57BL/6 * C57BL/6N * DBA/2)
|
abnormal sperm mitochondrial sheath morphology
|
J:245977
|
absent acrosome
|
J:245977
|
absent sperm mitochondrial sheath
|
J:245977
|
Slc9a9tm2d(KOMP)Wtsi/Slc9a9tm2d(KOMP)Wtsi
(involves: C57BL/6 * C57BL/6N * SJL)
|
abnormal cell physiology
|
J:258593
|
abnormal synaptic vesicle exocytosis
|
J:258593
|
Slc9c1tm1Gar/Slc9c1tm1Gar
(involves: 129S6/SvEvTac * C57BL/6J)
|
asthenozoospermia
|
J:87248
|
Slc11a2mk/Slc11a2mk
(MK/ReJ)
|
maternal effect
|
J:5167
|
Slc11a2mk/Slc11a2mk
(SEC.Cg-Slc11a2mk)
|
maternal effect
|
J:5167
|
Slc12a2em1Dlp/Slc12a2+
(involves: C57BL/6J * DBA/2J)
|
abnormal exocytosis
|
J:285398
|
Slc12a2em1Dlp/Slc12a2em1Dlp
(involves: C57BL/6J * DBA/2J)
|
abnormal exocytosis
|
J:285398
|
abnormal intestinal goblet cell physiology
|
J:285398
|
decreased colon goblet cell number
|
J:285398
|
Slc12a2tm1Bhk/Slc12a2tm1Bhk
(involves: 129P2/OlaHsd * C57BL/6J * DBA/2J)
|
abnormal spermatid morphology
|
J:60671
|
azoospermia
|
J:60671
|
decreased male germ cell number
|
J:60671
|
Slc12a2tm2Bhk/Slc12a2tm2Bhk
(involves: 129P2/OlaHsd * C57BL/6J * DBA/2J)
|
abnormal spermatid morphology
|
J:60671
|
azoospermia
|
J:60671
|
decreased male germ cell number
|
J:60671
|
Slc12a6tm1Tjj/Slc12a6tm1Tjj
(involves: 129/Sv * C57BL/6)
|
abnormal cell physiology
|
J:86183
|
Slc13a5tm1.2Helf/Slc13a5tm1.2Helf
(B6.Cg-Slc13a5tm1.2Helf)
|
abnormal hepatocyte mitochondrial morphology
|
J:176732
|
increased skeletal muscle cell glucose uptake
|
J:176732
|
Slc15a2tm1Dsmi/Slc15a2tm1Dsmi
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:81906
|
Slc16a7tm1.1Lupel/Slc16a7tm1.1Lupel
(C57BL/6J-Slc16a7tm1.1Lupel)
|
impaired neuron differentiation
|
J:296969
|
Slc16a13em1Tac/Slc16a13em1Tac
(C57BL/6N-Slc16a13em1Tac)
|
abnormal aerobic respiration
|
J:309785
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:309785
|
Slc17a5tm1Lex/Slc17a5tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal cell morphology
|
J:103485
|
Slc17a5tm1Lex/Slc17a5tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
decreased oligodendrocyte progenitor number
|
J:158444
|
Slc18a1tm1Dgen/Slc18a1tm1Dgen
(B6.129P2-Slc18a1tm1Dgen/J)
|
abnormal neuron proliferation
|
J:194189
|
increased neuron apoptosis
|
J:194189
|
Slc18a2tm1Uhl/Slc18a2+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:42811
|
Slc18a2tm2Kmo/Slc18a2tm2Kmo
(involves: 129P2/OlaHsd * C57BL/6)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:70606
|
Slc19a2tm1Ejn/Slc19a2tm1Ejn
(involves: 129S4/SvJae * 129S6/SvEvTac)
|
arrest of male meiosis
|
J:101675
|
azoospermia
|
J:101675
|
Slc19a2tm1Gelb/Slc19a2tm1Gelb
(involves: 129X1/SvJ)
|
arrest of male meiosis
|
J:87410
|
azoospermia
|
J:87410
|
decreased spermatid number
|
J:87410
|
Slc20a1tm1.2Lbek/Slc20a1tm1.2Lbek
(involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J)
|
decreased cell proliferation
|
J:157997
|
decreased hepatocyte proliferation
|
J:157997
|
increased hepatocyte apoptosis
|
J:157997
|
Slc22a3tm1Dpb/Slc22a3tm1Dpb
(involves: 129P2/OlaHsd)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:180517
|
Slc22a14em1Fjw/Slc22a14em1Fjw
(involves: C57BL/6N)
|
abnormal sperm annulus morphology
|
J:277914
|
abnormal sperm flagellum morphology
|
J:277914,
J:322731
|
asthenozoospermia
|
J:277914,
J:322731
|
decreased sperm progressive motility
|
J:277914
|
hairpin sperm flagellum
|
J:277914
|
impaired sperm migration in female genital tract
|
J:277914
|
kinked sperm flagellum
|
J:277914
|
Slc23a1tm1Mlev/Slc23a1tm1Mlev
(involves: 129S6/SvEvTac * C57BL/6J)
|
maternal effect
|
J:159697
|
Slc24a3em#Ebje/Slc24a3em#Ebje
(C57BL/6J-Slc24a3em#Ebje)
|
abnormal enterocyte proliferation
|
J:308448
|
Slc25a3tm1.1Jmol/Slc25a3tm1.1Jmol A1cfTg(Myh6-cre/Esr1*)1Jmk/?
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:229795
|
increased mitochondrial fission
|
J:229795
|
Slc25a4tm2Dwa/Slc25a4tm2Dwa
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal aerobic respiration
|
J:41256
|
Slc25a4tm2Dwa/Slc25a4tm2Dwa Slc25a5tm1Dwa/Y Speer6-ps1Tg(Alb-cre)21Mgn/?
(involves: 129S4/SvJae)
|
abnormal aerobic respiration
|
J:88165
|
Slc25a12Gt(OST123999)Lex/Slc25a12Gt(OST123999)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal aerobic respiration
|
J:101164
|
abnormal cellular respiration
|
J:243212
|
oxidative stress
|
J:193095
|
Slc25a17Gt(XB686)Byg/Slc25a17Gt(XB686)Byg
(involves: 129P2/OlaHsd * C57BL/6 * Swiss Webster)
|
increased hepatocyte apoptosis
|
J:291257
|
Slc25a19tm1Mjl/Slc25a19tm1Mjl
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss))
|
abnormal mitochondrial physiology
|
J:115337
|
Slc25a23tm1Lex/Slc25a23tm1Lex
(involves: 129 * C57BL/6)
|
abnormal mitochondrial physiology
|
J:196890
|
Slc25a25tm1.1Kz/Slc25a25tm1.1Kz
(involves: C57BL/6J * FVB/N)
|
abnormal cell physiology
|
J:170924
|
Slc25a28tm1.1Dwrd/Slc25a28tm1.1Dwrd Speer6-ps1Tg(Alb-cre)21Mgn/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCrl * DBA)
|
abnormal oxidative phosphorylation
|
J:300667
|
Slc25a28tm1.2Dwrd/Slc25a28tm1.2Dwrd
(involves: 129S6/SvEvTac * C57BL/6NCrl)
|
abnormal oxidative phosphorylation
|
J:300667
|
asthenozoospermia
|
J:300667
|
oligozoospermia
|
J:300667
|
Slc25a28tm1.2Dwrd/Slc25a28tm1.2Dwrd Slc25a37tm1.1Kapl/Slc25a37tm1.1Kapl Speer6-ps1Tg(Alb-cre)21Mgn/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCrl * DBA)
|
abnormal oxidative phosphorylation
|
J:300667
|
Slc25a31tm1Nte/Slc25a31tm1Nte
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal spermatocyte morphology
|
J:125346
|
arrest of male meiosis
|
J:125346
|
increased male germ cell apoptosis
|
J:125346
|
Slc25a37tm1.1Kapl/Slc25a37tm1.1Kapl Speer6-ps1Tg(Alb-cre)21Mgn/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCrl * DBA)
|
abnormal oxidative phosphorylation
|
J:300667
|
Slc25a46atc/Slc25a46atc
(B6.Cg-Slc25a46atc)
|
abnormal Purkinje cell mitochondrial morphology
|
J:242350
|
Slc25a48em1(IMPC)J/Slc25a48em1(IMPC)J
(involves: C57BL/6J * C57BL/6NJ)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:353858
|
abnormal mitochondrial crista morphology
|
J:353858
|
abnormal mitochondrial inner membrane morphology
|
J:353858
|
increased mitochondrial size
|
J:353858
|
oxidative stress
|
J:353858
|
Slc26a1tm1Mark/Slc26a1tm1Mark
(involves: 129X1/SvJ * CD-1)
|
abnormal vesicle-mediated transport
|
J:158567
|
Slc26a2tm1Aros/Slc26a2tm1Aros
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal cell physiology
|
J:97104
|
decreased cell proliferation
|
J:97104
|
Slc26a3tm1Sole/Slc26a3tm1Sole
(involves: 129S6/SvEvTac * C57BL/6)
|
increased cell proliferation
|
J:117587
|
Slc26a4pdsm/Slc26a4pdsm
(BXA7/PgnJ-Slc26a4pdsm/J)
|
asthenozoospermia
|
J:121997
|
oligozoospermia
|
J:121997
|
Slc26a8tm1Ggac/Slc26a8tm1Ggac
(involves: 129S/SvEvBrd)
|
abnormal sperm annulus morphology
|
J:125103
|
abnormal sperm midpiece morphology
|
J:125103
|
abnormal sperm mitochondrial morphology
|
J:125103
|
abnormal sperm mitochondrial sheath morphology
|
J:125103
|
asthenozoospermia
|
J:125103
|
hairpin sperm flagellum
|
J:125103
|
kinked sperm flagellum
|
J:125103
|
thin sperm flagellum
|
J:125103
|
Slc27a1tm1Jkk/Slc27a1tm1Jkk
(involves: 129S/SvEv * C57BL/6J)
|
abnormal skeletal muscle cell glucose uptake
|
J:88657
|
Slc27a2tm1Kds/Slc27a2tm1Kds
(involves: 129S4/SvJae * 129S6/SvEvTac)
|
abnormal cell physiology
|
J:83438
|
Slc27a4pskn/Slc27a4pskn
(involves: FVB)
|
increased keratinocyte proliferation
|
J:194779
|
Slc29a3tm1Lex/Slc29a3tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal lysosome physiology
|
J:179286
|
increased macrophage apoptosis
|
J:179286
|
Slc30a2tm1Kgna/Slc30a2tm1Kgna
(involves: 129 * C57BL/6)
|
decreased mammary gland epithelial cell proliferation
|
J:264481
|
increased mammary gland epithelial cell proliferation
|
J:264481
|
maternal effect
|
J:264481
|
Slc30a4lm/Slc30a4lm
(C57BL/6J-Slc30a4lm)
|
maternal effect
|
J:5911,
J:30724
|
Slc31a1tm1Jgt/Slc31a1tm1Jgt
(involves: 129X1/SvJ * C57BL/6)
|
abnormal basement membrane morphology
|
J:69862
|
Slc33a1tm1.1Lpu/Slc33a1+
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal autophagy
|
J:211266
|
Slc35c1tm1Cknr/Slc35c1tm1Cknr
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal leukocyte adhesion
|
J:121151
|
impaired leukocyte tethering or rolling
|
J:121151
|
Slc35e1em1Cya/Slc35e1em1Cya
(C57BL/6J-Slc35e1em1Cya)
|
decreased keratinocyte proliferation
|
J:340684
|
Slc37a4tm1Jyc/Slc37a4tm1Jyc
(involves: 129S4/SvJae * C57BL/6)
|
impaired neutrophil chemotaxis
|
J:86005
|
Slc38a2em1Zhxy/Slc38a2em1Zhxy
(129.B6-Slc38a2em1Zhxy)
|
increased ferroptosis
|
J:345023
|
Slc38a4em#Smtb/Slc38a4+
(C57BL/6NSlc-Slc38a4em#Ogu)
|
abnormal trophoblast giant cell proliferation
|
J:280426
|
Slc38a4em#Smtb/Slc38a4em#Smtb
(C57BL/6NSlc-Slc38a4em#Ogu)
|
abnormal trophoblast giant cell proliferation
|
J:280426
|
Slc39a3tm1Gka/Slc39a3tm1Gka
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
maternal effect
|
J:99161
|
Slc39a4tm1Gka/Slc39a4+
(involves: 129S1/Sv * C57BL/6 * FVB/N)
|
maternal effect
|
J:125096
|
Slc39a4tm2Gka/Slc39a4tm2Gka Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
abnormal small intestinal crypt cell proliferation
|
J:187178
|
Slc39a7tm1.1Tfk/Slc39a7tm1.1Tfk Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal enterocyte proliferation
|
J:236234
|
increased enterocyte apoptosis
|
J:236234
|
Slc39a8tm1.2Mrl/Slc39a8tm1.2Mrl
(B6(Cg)-Slc39a8tm1.2Mrl)
|
increased fetal cardiomyocyte proliferation
|
J:258360
|
Slc39a10tm1.1Tfk/Slc39a10tm1.1Tfk Tg(Foxn1-cre)8Ghr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased thymocyte apoptosis
|
J:254216
|
Slc39a13tm1Thir/Slc39a13tm1Thir
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoblast physiology
|
J:143911
|
Slc39a14tm1Lex/Slc39a14tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
decreased hepatocyte proliferation
|
J:236296
|
Slc40a1Pcm/Slc40a1+
(A.Cg-Slc40a1Pcm)
|
increased splenocyte apoptosis
|
J:98335
|
Slc40a1Pcm/Slc40a1Pcm
(A.Cg-Slc40a1Pcm)
|
increased splenocyte apoptosis
|
J:98335
|
Slc40a1tm1.1Mmfe/Slc40a1+
(involves: 129P2/OlaHsd * C57BL/6)
|
oxidative stress
|
J:215585
|
Slc40a1tm1.1Mmfe/Slc40a1tm1.1Mmfe
(involves: 129P2/OlaHsd * C57BL/6)
|
oxidative stress
|
J:215585
|
Slc41a1tm1.1Geno/Slc41a1tm1.1Geno
(involves: C57BL/6)
|
abnormal respiratory electron transport chain
|
J:304109
|
abnormal tricarboxylic acid cycle
|
J:304109
|
Slc52a3tm2a(KOMP)Wtsi/Slc52a3tm2a(KOMP)Wtsi
(involves: C57BL/6N)
|
decreased fatty acid beta-oxidation
|
J:236029
|
Slco2a1tm1.2Vsch/Slco2a1tm1.2Vsch
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * FVB/N)
|
abnormal cell physiology
|
J:168442
|
patent ductus arteriosus
|
J:168442
|
Slco2a1tm1Vsch/Slco2a1tm1Vsch
(involves: 129S6/SvEvTac * C57BL/6J)
|
patent ductus arteriosus
|
J:168442
|
Slfn2m1Btlr/Slfn2m1Btlr
(C57BL/6J-Slfn2m1Btlr)
|
abnormal T cell proliferation
|
J:158985
|
decreased T cell proliferation
|
J:158985
|
increased T cell apoptosis
|
J:158985
|
Slirptm1.2Pjle/Slirptm1.2Pjle
(involves: C57BL/6)
|
abnormal sperm annulus morphology
|
J:204433
|
abnormal sperm mitochondrial morphology
|
J:204433
|
decreased sperm progressive motility
|
J:204433
|
Slit1tm1.1Matl/Slit1tm1.1Matl Slit2tm1Matl/Slit2tm1Matl Slit3tm1.1Dor/Slit3+
(involves: 129S1/Sv * 129S2/SvPas)
|
abnormal axon guidance
|
J:89780
|
Slit1tm1.1Matl/Slit1tm1.1Matl Slit2tm1Matl/Slit2tm1Matl Slit3tm1.1Dor/Slit3tm1.1Dor
(involves: 129S1/Sv * 129S2/SvPas)
|
abnormal axon guidance
|
J:89780
|
Slit2tm1Matl/Slit2tm1Matl
(involves: 129S2/SvPas)
|
abnormal cell adhesion
|
J:106011
|
Slit2tm1Matl/Slit2tm1Matl Slit3tm1.1Dor/Slit3tm1.1Dor
(involves: 129S1/Sv * 129S2/SvPas)
|
increased mammary gland epithelial cell proliferation
|
J:141875
|
SlkGt(BC0415)Wtsi/SlkGt(BC0415)Wtsi
(involves: 129P2/OlaHsd * FVB/N)
|
decreased fibroblast proliferation
|
J:211339
|
increased embryonic tissue cell apoptosis
|
J:211339
|
increased placenta apoptosis
|
J:211339
|
Slpd1NZB/BlNJ/Slpd1NZB/BlNJ
(involves: DBA/2J * NZB/BlNJ)
|
increased B cell proliferation
|
J:124364
|
Slpitm1Nkw/Slpitm1Nkw
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:82214
|
Slu7tm1a(KOMP)Wtsi/Slu7+
(C57BL/6NTac-Slu7tm1a(KOMP)Wtsi/WtsiPh)
|
oxidative stress
|
J:345496
|
Slurp1tm1Lex/Slurp1tm1Lex
(Not Specified)
|
increased keratinocyte proliferation
|
J:210836
|
Slurp2tm1Lex/Slurp2tm1Lex
(involves: 129P2/OlaHsd * 129S5/SvEvBrd * C57BL/6)
|
increased keratinocyte proliferation
|
J:231067
|
Slx1btm1.1Jrou/Slx1btm1.1Jrou
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal DNA repair
|
J:204996
|
increased sensitivity to induced cell death
|
J:204996
|
induced chromosome breakage
|
J:204996
|
Slx4tm1.2Jrou/Slx4tm1.2Jrou
(B6.129P2-Slx4tm1.2Jrou)
|
abnormal DNA repair
|
J:204996
|
increased sensitivity to induced cell death
|
J:204996
|
induced chromosome breakage
|
J:204996
|
Slx4tm1a(EUCOMM)Wtsi/Slx4tm1a(EUCOMM)Wtsi
(C57BL/6N-Slx4tm1a(EUCOMM)Wtsi)
|
abnormal male germ cell apoptosis
|
J:168567
|
abnormal primordial germ cell morphology
|
J:168567
|
absent oocytes
|
J:168567
|
azoospermia
|
J:168567
|
chromosomal instability
|
J:168567
|
early cellular replicative senescence
|
J:168567
|
increased sensitivity to induced cell death
|
J:188123
|
oligozoospermia
|
J:168567
|
Slx4tm1Jrou/Slx4tm1Jrou
(Not Specified)
|
abnormal telomere morphology
|
J:202845
|
Slxem1.1JbmuSlxl1em1.1Jbmu/Y
(involves: C57BL/6NHsd * DBA/2NHsd * FVB/N)
|
globozoospermia
|
J:304511
|
oligozoospermia
|
J:304511
|
teratozoospermia
|
J:304511
|
Smad1tm1Abr/Smad1tm1.1Abr Tg(Col1a1-cre)1Kry/0
(involves: BALB/cJ * C57 * FVB)
|
decreased osteoblast proliferation
|
J:172689
|
impaired osteoblast differentiation
|
J:172689
|
Smad1tm1Rob/Smad1+ Smad5tm1Zuk/Smad5+
(involves: 129S/SvEv * 129S7/SvEvBrd)
|
absent primordial germ cells
|
J:119296
|
decreased primordial germ cell number
|
J:119296
|
Smad1tm1Rob/Smad1tm1Rob
(involves: 129S/SvEv * MF1)
|
decreased primordial germ cell number
|
J:71998
|
Smad1tm1Sor/Smad1tm1Sor
(involves: 129S4/SvJaeSor * C57BL/6)
|
absent primordial germ cells
|
J:90769
|
Smad1tm1Sor/Smad1tm1Sor
(129S4/SvJaeSor-Smad1tm1Sor)
|
absent primordial germ cells
|
J:90769
|
Smad1tm1Sor/Smad1tm2Sor
(involves: 129S4/SvJaeSor * C57BL/6)
|
decreased primordial germ cell number
|
J:90769
|
Smad1tm1Tako/Smad1tm1Tako
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2)
|
absent primordial germ cells
|
J:79513
|
decreased primordial germ cell number
|
J:79513
|
Smad1tm2Sor/Smad1tm2Sor
(involves: 129S4/SvJaeSor * C57BL/6)
|
abnormal cell morphology
|
J:90769
|
absent primordial germ cells
|
J:90769
|
Smad1tm2Sor/Smad1tm2Sor
(129S4/SvJaeSor-Smad1tm2Sor)
|
abnormal cell morphology
|
J:90769
|
absent primordial germ cells
|
J:90769
|
Smad2tm1.1Epb/Smad2tm1.1Epb Smad3tm1Cxd/Smad3tm1Cxd
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal cell morphology
|
J:119642
|
decreased apoptosis
|
J:119642
|
Smad2tm1.1Epb/Smad2tm1.1Epb Smad3tm1Cxd/Smad3tm1Cxd Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * DBA * SJL)
|
abnormal cell morphology
|
J:119642
|
abnormal cell physiology
|
J:119642
|
Smad2tm1.1Epb/Smad2tm1.1Epb Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129/Sv * C57BL/6 * DBA * SJL)
|
abnormal cell differentiation
|
J:119642
|
abnormal cell migration
|
J:119642
|
increased hepatocyte proliferation
|
J:119642
|
Smad2tm1.1Nomu/Smad2tm1.1Nomu Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
abnormal cerebellar granule cell migration
|
J:173787
|
increased neuron apoptosis
|
J:173787
|
Smad2tm1Cxd/Smad2+ Smad3tm1Cxd/Smad3+
(involves: 129S6/SvEvTac * NIH Black Swiss)
|
abnormal hepatoblast migration
|
J:106308
|
decreased hepatocyte proliferation
|
J:70388
|
Smad2tm1Xya/Smad2tm1Xya Tg(KRT5-cre)1Xya/0
(involves: 129S6/SvEvTac)
|
increased keratinocyte migration
|
J:178733
|
Smad3tm1Cxd/Smad3tm1Cxd
(either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * NIH Black Swiss))
|
impaired neutrophil chemotaxis
|
J:53510
|
Smad3tm1Cxd/Smad3tm1Cxd
(B6.129S6-Smad3tm1Cxd)
|
decreased renal tubule apoptosis
|
J:102084
|
Smad3tm1Cxd/Smad3tm1Cxd
(involves: 129S6/SvEvTac)
|
decreased B cell apoptosis
|
J:140567
|
Smad3tm1Xfw/Smad3tm1Xfw
(involves: 129/Sv * C57BL/6)
|
abnormal B cell proliferation
|
J:53948
|
abnormal cell proliferation
|
J:53948
|
abnormal T cell proliferation
|
J:53948
|
Smad4tm1Cxd/Smad4tm1Cxd
(involves: 129S6/SvEvTac)
|
decreased cell proliferation
|
J:46852
|
decreased embryonic epiblast cell proliferation
|
J:46852
|
decreased inner cell mass proliferation
|
J:46852
|
Smad4tm1Mak/Smad4tm1Mak
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * C57BL/6J * CD-1))
|
decreased cell proliferation
|
J:45399
|
Smad4tm1Rob/Smad4tm1.1Rob Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S/SvEv * CD-1)
|
absent primordial germ cells
|
J:92066
|
Smad4tm2.1Cxd/Smad4tm2.1Cxd Tg(Dppa3-cre/Esr1*)3Sait/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA)
|
abnormal male meiosis
|
J:191052
|
Smad4tm2.1Cxd/Smad4tm2.1Cxd Tg(KRT5-cre)1Xya/0
(involves: 129S6/SvEvTac)
|
increased keratinocyte proliferation
|
J:101602
|
Smad4tm2.1Cxd/Smad4tm2.1Cxd Tg(Pou5f1-cre/ERT2)#Ysa/0
(involves: 129S6/SvEvTac)
|
abnormal male meiosis
|
J:191052
|
Smad4tm2.1Cxd/Smad4tm2.1Cxd Tg(Sp7-tTA,tetO-EGFP/cre)1Amc/0
(involves: 129S6/SvEvTac * C57BL/6J * CD-1)
|
abnormal osteoblast physiology
|
J:211171
|
Smad5tm1Cxd/Smad5tm1Cxd
(either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * NIH Black Swiss))
|
increased apoptosis
|
J:53289
|
Smad5tm1Zuk/Smad5+
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased primordial germ cell number
|
J:70069
|
Smad5tm1Zuk/Smad5+ Smad9tm2.1Rob/Smad9tm2.1Rob
(involves: 129S/SvEv * 129S7/SvEvBrd)
|
abnormal germ cell morphology
|
J:119296
|
Smad5tm1Zuk/Smad5tm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased primordial germ cell number
|
J:70069
|
Smad7Gt(YHC053)Byg/Smad7+ Tbx1tm1Bld/Tbx1+
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J)
|
increased vascular smooth muscle cell proliferation
|
J:212881
|
Smad7tm1.1Ink/Smad7tm1.1Ink Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:184670
|
Smad7tm1Gkg/Smad7tm1Gkg Tg(Pdx1-cre/Esr1*)#Dam/0
(involves: C57BL/6 * CBA)
|
abnormal pancreatic beta cell differentiation
|
J:198451
|
Smad7tm1Rheu/Smad7tm1Rheu
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
decreased B cell proliferation
|
J:120714
|
increased B cell apoptosis
|
J:120714
|
Smap1tm1.1Sata/Smap1tm1.1Sata
(B6.Cg-Smap1tm1.1Sata)
|
abnormal endocytosis
|
J:196385
|
Smap1tm1.1Sata/Smap1tm1.1Sata Smap2tm1Sata/Smap2tm1Sata
(involves: 129P2/OlaHsd * C57BL/6NCrlj * CBA/JNCrlj)
|
increased embryonic tissue cell apoptosis
|
J:226700
|
Smap2tm1Sata/Smap2tm1Sata
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal acrosome assembly
|
J:230490
|
abnormal acrosome morphology
|
J:230490
|
abnormal proacrosomal vesicle fusion
|
J:230490
|
abnormal sperm mitochondrial sheath morphology
|
J:230490
|
asthenozoospermia
|
J:230490
|
detached acrosome
|
J:230490
|
ectopic manchette
|
J:230490
|
globozoospermia
|
J:230490
|
Smarca1tm1.1Pick/Y
(involves: 129S4/SvJae * CD-1)
|
abnormal mitosis
|
J:183998
|
abnormal neuron differentiation
|
J:183998
|
abnormal neuronal precursor proliferation
|
J:183998
|
Smarca1tm1.1Pick/Smarca1tm1.1Pick
(involves: 129S4/SvJae * CD-1)
|
abnormal mitosis
|
J:183998
|
abnormal neuron differentiation
|
J:183998
|
abnormal neuronal precursor proliferation
|
J:183998
|
Smarca4tm1.1Pcn/Smarca4+
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
patent ductus arteriosus
|
J:172661
|
Smarca4tm1.2Pcn/Smarca4tm1.1Pcn Tg(Myh11-cre,-EGFP)2Mik/0
(involves: 129S2/SvPas * C57BL/6 * DBA/2)
|
patent ductus arteriosus
|
J:172661
|
Smarca4tm1Mag/Smarca4tm1.2Pcn
(involves: 129S2/SvPas)
|
cellular phenotype
|
J:66861
|
Smarca5tm1Ais/Smarca5tm1Ais
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal inner cell mass apoptosis
|
J:86695
|
absent inner cell mass proliferation
|
J:86695
|
increased trophectoderm apoptosis
|
J:86695
|
Smarcad1tm1Gos/Smarcad1tm1Gos
(involves: 129S2/SvPas * C57BL/6)
|
decreased oocyte number
|
J:56661
|
Smarcad1tm1Gos/Smarcad1tm1Gos
(129S2/SvPas-Smarcad1tm1Gos)
|
decreased oocyte number
|
J:56661
|
Smarcal1tm1.1Cfbo/Smarcal1tm1.1Cfbo
(either: B6.129-Smarcal1tm1.1Cfbo or (involves: 129 * C57BL/6))
|
decreased fibroblast proliferation
|
J:183899
|
Smarcb1em1Koke/Smarcb1em1Koke
(C57BL/6-Smarcb1em1Koke)
|
cellular phenotype
|
J:337790
|
Smarcb1Gt(OST32815)Lex/Smarcb1Gt(OST32815)Lex
(either: (involves: 129 * 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6))
|
absent inner cell mass proliferation
|
J:69009
|
absent trophectoderm cell proliferation
|
J:69009
|
Smarcb1tm1Mya/Smarcb1tm1Mya
(involves: 129S2/SvPas * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:68501
|
increased trophectoderm apoptosis
|
J:68501
|
Smarcb1tm1Mya/Smarcb1tm2Mya Tg(Alb1-cre)7Gsc/0
(involves: 129S2/SvPas * FVB/N)
|
increased hepatocyte proliferation
|
J:103919
|
Smarcb1tm1Sho/Smarcb1tm3Sho Tg(Mx1-cre)1Cgn/?
(involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6 * CBA)
|
increased apoptosis
|
J:80224
|
Smarcb1tm2Sho/Smarcb1tm2Sho Tg(GFAP-cre)#Gtm/0
(involves: 129S1/Sv * C57BL/6 * CBA)
|
abnormal cerebellar granule cell migration
|
J:226786
|
Smarcb1tm2Sho/Smarcb1tm2Sho Trp53tm1Brn/Trp53tm1Brn Tg(GFAP-cre)#Gtm/0
(involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA)
|
abnormal cerebellar granule cell migration
|
J:226786
|
Smarcc1tm2.1Rhs/Smarcc1tm2.1Rhs Tg(Mx1-cre)1Cgn/0
(involves: BALB/c * C57BL/6 * CBA)
|
decreased B cell proliferation
|
J:184060
|
increased B cell apoptosis
|
J:184060
|
Smarcc2tm1.1Stoy/Smarcc2tm1.1Stoy
(involves: 129S1/Sv * C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:197141
|
Smarcc2tm1.1Stoy/Smarcc2tm1.1Stoy Emx1tm1(cre)Krj/Emx1+
(involves: 129S1/Sv * 129S2/SvPas * C57BL/6)
|
abnormal DNA methylation
|
J:197141
|
abnormal neuron differentiation
|
J:197141
|
abnormal neuronal precursor proliferation
|
J:197141
|
Smarcd3tm1.1Bbr/Smarcd3tm1.1Bbr Tg(Myh6-cre)2182Mds/0
(either: (involves: 129 * C57BL/6 * FVB/N * SJL) or (involves: 129 * C57BL/6 * FVB/N * ICR * SJL))
|
cardiac interstitial fibrosis
|
J:257963
|
increased cardiomyocyte apoptosis
|
J:257963
|
Smarcd3tm1.2Bbr/Smarcd3tm1.2Bbr
(either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * ICR * SJL))
|
decreased fetal cardiomyocyte proliferation
|
J:257963
|
Smc1atm1Mbk/Y
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:104490
|
abnormal cell death
|
J:104490
|
chromosome breakage
|
J:104490
|
increased cellular sensitivity to ionizing radiation
|
J:104490
|
increased cellular sensitivity to methylmethanesulfonate
|
J:104490
|
Smc1bm1Ham/Smc1bm1Ham
(involves: C57BL/6JJcl * DBA/2JJcl * ICR)
|
abnormal male germ cell apoptosis
|
J:164958
|
azoospermia
|
J:164958
|
Smc1btm1Jess/Smc1btm1Jess
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal female meiosis
|
J:96769
|
abnormal male meiosis
|
J:96769
|
arrest of male meiosis
|
J:96769
|
azoospermia
|
J:96769
|
Smc1btm1Jess/Smc1btm2.2Jess
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
azoospermia
|
J:166776
|
Smc2tm1.1Hiran/Smc2tm1.2Hiran Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal cell nucleus morphology
|
J:222181
|
abnormal mitosis
|
J:222181
|
Smchd1MommeD1/Smchd1+
(FVB/NJ-Smchd1MommeD1)
|
abnormal imprinting
|
J:99816
|
Smchd1MommeD1/Smchd1+
(involves: C57BL/6 * FVB/N)
|
abnormal DNA methylation
|
J:142334
|
Smchd1MommeD1/Smchd1MommeD1
(FVB/NJ-Smchd1MommeD1)
|
abnormal imprinting
|
J:99816
|
Smchd1MommeD1/Smchd1MommeD1
(involves: C57BL/6 * FVB/N)
|
abnormal DNA methylation
|
J:142334
|
Smcptm1Wen/Smcptm1Wen
(involves: 129S1/Sv * 129X1/SvJ)
|
asthenozoospermia
|
J:78930
|
Smcr8em1Btlr/Smcr8em1Btlr
(C57BL/6J-Smcr8em1Btlr)
|
abnormal lysosome morphology
|
J:268243
|
abnormal lysosome physiology
|
J:268243
|
Smcr8tm1(KOMP)Vlcg/Smcr8tm1(KOMP)Vlcg
(involves: 129S1/SvImJ * C57BL/6NTac)
|
abnormal autophagy
|
J:236977
|
abnormal lysosome physiology
|
J:236977
|
Smcr8tm1.1(KOMP)Vlcg/Smcr8tm1.1(KOMP)Vlcg
(involves: 129S1/SvImJ * C57BL/6J * C57BL/6NTac)
|
abnormal autophagy
|
J:236977
|
abnormal lysosome physiology
|
J:236977
|
Smdq1BALB/c/Smdq1CAST/EiJ
(involves: BALB/c * CAST/Ei)
|
abnormal mitochondrial fission
|
J:81446
|
Smdq1CAST/EiJ/Smdq1CAST/EiJ
(involves: BALB/c * CAST/Ei)
|
abnormal mitochondrial fission
|
J:81446
|
Smdq2CAST/EiJ/Smdq2CAST/EiJ
(involves: BALB/c * CAST/Ei)
|
abnormal mitochondrial fission
|
J:81446
|
Smdq3BALB/c/?
(involves: BALB/c * CAST/Ei)
|
abnormal mitochondrial fission
|
J:81446
|
Smdt1em1Fink/Smdt1+
(involves: C57BL/6J * CBA)
|
cellular phenotype
|
J:238984
|
Smdt1em2Fink/Smdt1em2Fink
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
abnormal fibroblast physiology
|
J:287405
|
abnormal mitochondrial physiology
|
J:287405
|
Smdt1tm1c(EUCOMM)Wtsi/Smdt1tm1c(EUCOMM)Wtsi Tg(Ckmm-cre)5Khn/0
(involves: 129S4/SvJae * C57BL/6N * FVB)
|
abnormal mitochondrial physiology
|
J:287405
|
Smg1Gt(AG0297)Wtsi/Smg1+
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:193626
|
Smg1Gt(RRT449)Byg/Smg1Gt(RRT449)Byg
(B6.129P2-Smg1Gt(RRT449)Byg)
|
abnormal cell physiology
|
J:196053
|
decreased cell proliferation
|
J:196053
|
increased embryonic tissue cell apoptosis
|
J:196053
|
Smg6tm1.1Zqw/Smg6tm1.1Zqw Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
abnormal cell morphology
|
J:222980
|
abnormal cell physiology
|
J:222980
|
abnormal telomere morphology
|
J:222980
|
cellular phenotype
|
J:222980
|
Smg6tm1.2Zqw/Smg6tm1.2Zqw
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased inner cell mass proliferation
|
J:222980
|
Smn1tm1Msd/Smn1tm1Msd
(involves: 129P2/OlaHsd * MF1)
|
abnormal apoptosis
|
J:42813
|
Smn1tm1Msd/Smn1tm1Msd Grm7Tg(SMN2)89Ahmb/Grm7Tg(SMN2)89Ahmb Tg(SMN2*delta7)4299Ahmb/0
(FVB.Cg-Grm7Tg(SMN2)89Ahmb Smn1tm1Msd Tg(SMN2*delta7)4299Ahmb/J)
|
cardiac interstitial fibrosis
|
J:194969
|
Smn1tm1Msd/Smn1tm1Msd Grm7Tg(SMN2)89Ahmb/Grm7Tg(SMN2)89Ahmb Tg(SMN2*delta7)4299Ahmb/Tg(SMN2*delta7)4299Ahmb
(involves: 129P2/OlaHsd * FVB/N)
|
cardiac interstitial fibrosis
|
J:164444
|
oxidative stress
|
J:164444
|
Smn1tm1Msd/Smn1tm1Msd Tg(SMN1-SMN2*)16Cll/0 Grm7Tg(SMN2)89Ahmb/Grm7Tg(SMN2)89Ahmb
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
cardiac interstitial fibrosis
|
J:194969
|
Smotm1Amc/Smotm2Amc Isl1tm1(cre)Sev/Isl1+
(involves: 129S/Sv * 129X1/SvJ)
|
abnormal cardiac neural crest cell migration
|
J:110602
|
Smotm1Amc/Smotm2Amc Tg(Col2a1-cre)10Amc/0
(involves: 129X1/SvJ)
|
decreased chondrocyte proliferation
|
J:73071
|
Smotm2Amc/Smotm2.1Amc H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129X1/SvJ * C57BL/6J * CBA/J)
|
abnormal neural crest cell apoptosis
|
J:135134
|
Smotm2Amc/Smotm2.1Amc H2az2Tg(Wnt1-cre)11Rth/H2az2+ Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
(involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J * CBA/J)
|
impaired cardiac neural crest cell differentiation
|
J:135134
|
Smotm2Amc/Smotm2.1Amc Nkx2-5tm1(cre)Rjs/Nkx2-5+
(involves: 129S7/SvEvBrd * 129X1/SvJ)
|
abnormal neural crest cell apoptosis
|
J:135134
|
abnormal neural crest cell migration
|
J:135134
|
Smotm2Amc/Smotm2Amc Nkx3-2tm1(cre)Wez/Nkx3-2+
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ)
|
abnormal enterocyte proliferation
|
J:199664
|
abnormal intestinal goblet cell morphology
|
J:199664
|
Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak/Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak
(involves: C3H * C57BL/6J * DBA/2)
|
abnormal interdigital cell death
|
J:169180
|
Smpd1tm1Esc/Smpd1tm1Esc
(involves: 129S1/Sv * C57BL/6J)
|
abnormal apoptosis
|
J:35076
|
abnormal male germ cell morphology
|
J:78875
|
asthenozoospermia
|
J:78875
|
increased macrophage derived foam cell number
|
J:81982
|
teratozoospermia
|
J:78875
|
Smpd1tm1Esc/Smpd1tm1Esc
(involves: 129S1/Sv)
|
abnormal neuron differentiation
|
J:199833
|
Smpd1tm1Wst/Smpd1tm1Wst
(involves: 129P2/OlaHsd * C57BL/6)
|
increased macrophage derived foam cell number
|
J:26748
|
Smstm1a(EUCOMM)Wtsi/Y
(involves: C57BL/6 * C57BL/6N)
|
oligozoospermia
|
J:213427
|
Smug1tm1a(EUCOMM)Hmgu/Smug1tm1a(EUCOMM)Hmgu
(involves: C57BL/6 * C57BL/6N)
|
abnormal base-excision repair
|
J:197809
|
decreased sensitivity to induced cell death
|
J:197809
|
Smug1tm1a(EUCOMM)Hmgu/Smug1tm1a(EUCOMM)Hmgu
(involves: C57BL/6 * C57BL/6N)
|
abnormal base-excision repair
|
J:197809
|
decreased sensitivity to induced cell death
|
J:197809
|
Smug1tm1a(EUCOMM)Hmgu/Smug1tm1a(EUCOMM)Hmgu Ungtm1Tld/Ungtm1Tld
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N)
|
abnormal base-excision repair
|
J:197809
|
abnormal mismatch repair
|
J:197809
|
Smug1tm1a(EUCOMM)Hmgu/Smug1tm1a(EUCOMM)Hmgu Ungtm1Tld/Ungtm1Tld
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6N)
|
abnormal base-excision repair
|
J:197809
|
abnormal mismatch repair
|
J:197809
|
Smurf1tm1Yez/Smurf1tm1Yez
(either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * NIH Black Swiss))
|
abnormal osteoblast physiology
|
J:97303
|
Smurf2Gt(RRA098)Byg/Smurf2+
(involves: 129P2/OlaHsd * C57BL/6)
|
delayed cellular replicative senescence
|
J:189320
|
Smurf2Gt(RRA098)Byg/Smurf2Gt(RRA098)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
delayed cellular replicative senescence
|
J:189320
|
Smurf2tm1Yez/Smurf2tm1Yez
(either: B6.129S6-Smurf2tm1Yez or (involves: 129S6/SvEvTac * NIH Black Swiss))
|
abnormal cell physiology
|
J:180221
|
Smyd1tm1Dsr/Smyd1tm1Dsr
(involves: 129S6/SvEvTac)
|
abnormal apoptosis
|
J:76212
|
Snai1tm1.1Stjw/Snai1+
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal cell migration
|
J:146645
|
abnormal cell physiology
|
J:146645
|
Snap29tm1b(EUCOMM)Wtsi/Snap29tm1b(EUCOMM)Wtsi
(involves: C57BL/6N * FVB/N)
|
abnormal autophagy
|
J:236759
|
abnormal endoplasmic reticulum physiology
|
J:236759
|
increased endoplasmic reticulum stress
|
J:236759
|
Snap29tm1c(EUCOMM)Wtsi/Snap29tm1c(EUCOMM)Wtsi Tg(KRT14-cre)1Cgn/0
(involves: C57BL/6 * C57BL/6N * DBA/2)
|
abnormal keratinocyte differentiation
|
J:236759
|
increased keratinocyte proliferation
|
J:236759
|
Snapintm1Zhs/Snapintm1Zhs
(involves: 129S6/SvEvTac)
|
abnormal cell physiology
|
J:207508
|
Sncatm1Rosl/Sncatm1Rosl
(B6.129X1-Sncatm1Rosl)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:92213
|
Sncatm1Rosl/Sncatm1Rosl Sncgtm1Vlb/Sncgtm1Vlb
(B6.129-Sncatm1Rosl Sncgtm1Vlb)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:92213
|
Sncatm1Wtd/Sncatm1Wtd
(involves: 129)
|
abnormal respiratory electron transport chain
|
J:79993
|
cellular phenotype
|
J:101289
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:79993
|
Sncgtm1Vlb/Sncgtm1Vlb
(B6.129P2-Sncgtm1Vlb)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:92213
|
Snhg15tm1Nju/Snhg15tm1Nju
(involves: C57BL/6J)
|
abnormal mitotic spindle morphology
|
J:291983
|
Snord115em1Jcav/Snord115+
(B6.Cg-Snord115em1Jcav)
|
maternal imprinting
|
J:305741
|
Snord116tm1.1Uta/Snord116+
(involves: C57BL/6J)
|
maternal imprinting
|
J:131662
|
Snord116tm1Uta/Snord116+ Tg(Zp3-cre)93Knw/0
(involves: C57BL/6J)
|
maternal imprinting
|
J:131427
|
Snphtm1Zhs/Snphtm1Zhs
(involves: 129S6/SvEvTac)
|
abnormal mitochondrial morphology
|
J:145318
|
abnormal mitochondrial physiology
|
J:145318
|
Snrnp40em1Btlr/Snrnp40swp
(C57BL/6J-Snrnp40em1Btlr/Snrnp40swp)
|
decreased T cell proliferation
|
J:282417
|
Snrpntm1Alb/Snrpn+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
cellular phenotype
|
J:70275
|
Snrpntm1Rsnk/Snrpn+
(either: 129S1-Snrpntm1Rsnk or (involves: 129S1/Sv * C57BL/6J))
|
abnormal imprinting
|
J:105412
|
maternal imprinting
|
J:105412
|
Snrpntm2.1Kaj/Snrpn+ Alpltm1(cre)Nagy/Alpl+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal DNA methylation
|
J:174457
|
Snrpntm2Alb/Snrpn+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
cellular phenotype
|
J:70275
|
Snrpntm2Cbr/Snrpn+
(involves: 129S1/Sv * C57BL/6)
|
maternal imprinting
|
J:105412,
J:47318
|
Snrpntm2Cbr/Snrpn+
(either: (involves: 129S1/Sv * C57BL/6J) or (involves: 129S1/Sv * BALB/c * C57BL/6J) or (involves: 129S1/Sv * C3H/HeJ * C57BL/6J) or (involves: 129S1/Sv * C57BL/6J * FVB/NJ))
|
maternal imprinting
|
J:94414
|
Snrpntm2Cbr/Snrpn+
(either: B6.Cg-Snrpntm2Cbr or (involves: 129S1/Sv * C57BL/6J * DBA/2J))
|
maternal imprinting
|
J:94414
|
Snrpntm2Cbr/Snrpntm1Rsnk
(involves: 129S1/Sv * C57BL/6)
|
maternal imprinting
|
J:105412
|
Snrpntm5Alb/Snrpn+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal DNA methylation
|
J:105289
|
genetic imprinting
|
J:105289
|
Snx27tm1Lslo/Snx27tm1Lslo
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:171001
|
Socs3tm1Wsa/Socs3tm2Wsa Tg(Vav1-cre)1Awr/0
(involves: C57BL/6)
|
abnormal granulocyte differentiation
|
J:89785
|
Sod1m1H/Sod1+
(involves: C3H/HeH * C57BL/6J)
|
abnormal mitochondrial physiology
|
J:219360
|
Sod1tm1Cje/Sod1tm1Cje
(involves: C57BL/6J * CD-1)
|
decreased fibroblast proliferation
|
J:42265
|
increased fibroblast apoptosis
|
J:42265
|
Sod1tm1Dkd/Sod1tm1Dkd
(involves: 129S1/Sv * 129X1/SvJ)
|
oxidative stress
|
J:60470
|
Sod1tm1Leb/Sod1tm1Leb
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal mitochondrial morphology
|
J:219024
|
dilated mitochondrion
|
J:219024
|
disorganized mitochondrial cristae
|
J:219024
|
oxidative stress
|
J:219024
|
Sod2tm1(rtTA*M2,tetO)Jsg/Sod2tm1(rtTA*M2,tetO)Jsg
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:209713
|
abnormal redox activity
|
J:209713
|
increased cell death
|
J:209713
|
increased cellular sensitivity to gamma-irradiation
|
J:209713
|
Sod2tm1(tetO-Sod2)Evbo/Sod2+
(involves: 129S4/SvJae * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:162190
|
Sod2tm1(tetO-Sod2)Evbo/Sod2tm1(tetO-Sod2)Evbo
(involves: 129S4/SvJae * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:162190
|
oxidative stress
|
J:162190
|
Sod2tm1.1Kskk/Sod2+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:98289
|
oxidative stress
|
J:98289
|
Sod2tm1.1Kskk/Sod2tm1.1Kskk
(involves: 129P2/OlaHsd * C57BL/6)
|
oxidative stress
|
J:98289
|
Sod2tm1Cje/Sod2+
(B6.Cg-Sod2tm1Cje/Mmmh)
|
abnormal mitochondrial physiology
|
J:108637
|
abnormal respiratory electron transport chain
|
J:108637
|
oxidative stress
|
J:87514,
J:108637
|
Sod2tm1Cje/Sod2+
(involves: C57BL/6J * CD-1)
|
abnormal mitochondrial physiology
|
J:67874
|
abnormal respiratory electron transport chain
|
J:67874
|
increased hepatocyte apoptosis
|
J:67874
|
oxidative stress
|
J:67874
|
Sod2tm1Cje/Sod2+
(D2.Cg-Sod2tm1Cje)
|
abnormal mitochondrial physiology
|
J:73998
|
Sod2tm1Cje/Sod2+
(involves: C57BL/6J * DBA/2J)
|
abnormal tricarboxylic acid cycle
|
J:73998
|
Sod2tm1Cje/Sod2tm1Cje
(involves: C57BL/6J * CD-1)
|
abnormal aerobic respiration
|
J:52592
|
abnormal cell physiology
|
J:52592
|
abnormal tricarboxylic acid cycle
|
J:29899,
J:52592
|
Sod2tm1Cje/Sod2tm1Cje
(B6.Cg-Sod2tm1Cje/Mmmh)
|
oxidative stress
|
J:108637
|
Sod2tm1Cje/Sod2tm1Cje
(D2.Cg-Sod2tm1Cje)
|
abnormal mitochondrial physiology
|
J:73998
|
Sod2tm1Cje/Sod2tm1Cje
(involves: C57BL/6J * DBA/2J)
|
abnormal tricarboxylic acid cycle
|
J:73998,
J:98007
|
Sod2tm1Kskk/Sod2tm1Kskk Tg(BEST1-rtTA,tetO-cre)1Yzl/0
(B6J.Cg-Sod2tm1Kskk Tg(BEST1-rtTA,tetO-cre)1Yzl)
|
oxidative stress
|
J:230153
|
Sod2tm1Leb/Sod2tm1Leb
(B6.129S7-Sod2tm1Leb/J)
|
abnormal mitochondrial physiology
|
J:36148
|
Sod2tm1Shs/Sod2+ Tg(Cdh16-cre)91Igr/0
(involves: C57BL/6 * C57BL/6CrSlc)
|
oxidative stress
|
J:174099
|
Sod2tm1Shs/Sod2tm1Shs Tg(Cdh16-cre)91Igr/0
(involves: C57BL/6 * C57BL/6CrSlc)
|
oxidative stress
|
J:174099
|
Sod2tm1Shs/Sod2tm1Shs Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6CrSlc * FVB)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:117386
|
abnormal mitochondrial crista morphology
|
J:117386
|
abnormal oxidative phosphorylation
|
J:117386
|
cardiac interstitial fibrosis
|
J:117386
|
decreased mitochondrial size
|
J:117386
|
oxidative stress
|
J:117386
|
Sod2tm1Shs/Sod2tm1Shs Tg(Ckmm-cre)5Khn/0
(involves: FVB)
|
cardiac interstitial fibrosis
|
J:171017
|
oxidative stress
|
J:171017
|
Sod2tm1Shs/Sod2tm1Shs Tg(TNNI2-icre)1Vrmn/0
(involves: C57BL/6)
|
abnormal mitochondrial physiology
|
J:155917
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:155917
|
increased muscle cell glucose uptake
|
J:155917
|
Sod2tm1Smel/Sod2tm1Smel Tg(KRT14-cre/ERT)20Efu/0
(involves: C57BL/6J * CD-1)
|
abnormal keratinocyte differentiation
|
J:226565
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:226565
|
decreased keratinocyte proliferation
|
J:226565
|
early cellular replicative senescence
|
J:226565
|
Sohlh1tm1Rajk/Sohlh1tm1Rajk
(involves: 129S5/SvEvBrd * 129S7/SvEvBrd * C57BL/6)
|
abnormal oogenesis
|
J:110210
|
absent oocytes
|
J:110210
|
decreased oocyte number
|
J:110210
|
Sohlh2tm1Fkh/Sohlh2tm1Fkh
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal spermatocyte morphology
|
J:220953
|
abnormal spermatogonia morphology
|
J:220953
|
decreased male germ cell number
|
J:220953
|
Sohlh2tm1Miya/Sohlh2tm1Miya
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal oogenesis
|
J:143535
|
abnormal spermatocyte morphology
|
J:143535
|
abnormal spermatogonia morphology
|
J:143535
|
Sohlh2tm1Rajk/Sohlh2tm1Rajk
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased oocyte number
|
J:145802
|
impaired granulosa cell differentiation
|
J:145802
|
Sorbs3tm1Kiok/Sorbs3tm1Kiok
(B6.Cg-Sorbs3tm1Kiok)
|
abnormal cell migration
|
J:162344
|
Sort1tm1Camo/Sort1tm1Camo
(B6.129X1-Sort1tm1Camo)
|
abnormal lysosome morphology
|
J:154468
|
Sos1tm1.1Les/Sos1tm1.1Les Tg(Lck-cre)1Cwi/0
(involves: 129 * C57BL/6)
|
decreased T cell proliferation
|
J:174536
|
Sos1tm1.2Rak/Sos1+
(involves: 129S/Sv * C57BL/6 * FVB/N * SJL)
|
abnormal fetal cardiomyocyte proliferation
|
J:171873
|
cardiac interstitial fibrosis
|
J:171873
|
increased cardiomyocyte apoptosis
|
J:171873
|
Sos1tm1.2Rak/Sos1tm1.2Rak
(involves: 129S/Sv * C57BL/6 * FVB/N * SJL)
|
abnormal fetal cardiomyocyte proliferation
|
J:171873
|
Sosttm1(KOMP)Vlcg/Sosttm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
decreased osteocyte apoptosis
|
J:167585
|
Sosttm1Lhe/Sosttm1Lhe
(involves: C57BL/6J)
|
abnormal osteoblast physiology
|
J:168665
|
decreased osteoblast apoptosis
|
J:168665
|
decreased osteocyte apoptosis
|
J:168665
|
Sosttm1Paz/Sosttm1Paz
(involves: 129/Sv * Black Swiss)
|
abnormal osteoblast physiology
|
J:150166
|
Sostdc1tm1Myan/Sostdc1tm1Myan
(involves: 129X1/SvJ * C57BL/6J)
|
decreased renal tubule apoptosis
|
J:105264
|
Sostdc1tm1Snd/Sostdc1tm1Snd
(involves: C57BL/6)
|
abnormal osteoblast physiology
|
J:216098
|
decreased chondrocyte proliferation
|
J:216098
|
increased osteoblast proliferation
|
J:216098
|
Sox1tm1Vep/Sox1tm2Vep
(involves: 129S/SvEv)
|
abnormal neuronal migration
|
J:99610
|
Sox2tm1.1Lan/Sox2tm1.1Lan Tg(Scgb1a1-cre)1Kkw/0
(involves: 129/Sv * C57BL/6)
|
absent respiratory motile cilia
|
J:155963
|
Sox2tm1.2Lan/Sox2tm1.2Lan Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: C57BL/6 * C57BL/6NCrlj * DBA/2 * FVB/N)
|
abnormal autophagy
|
J:205532
|
Sox2tm1Okud/Sox2tm1Okud Tg(Nes-cre)1Sasa/?
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:138323
|
Sox2tm1Rlb/Sox2+
(involves: 129S/SvEv * MF1)
|
oligozoospermia
|
J:114458
|
Sox2tm2Skn/Sox2tm3Skn
(involves: 129S/SvEv * 129S1/Sv * C57BL/6J)
|
abnormal neuron differentiation
|
J:92063
|
Sox2tm2Skn/Sox2tm4.1Skn Tg(Nes-cre)1Kln/0
(either: (involves: 129S/Sv * C57BL/6 * SJL) or (involves: 129S/Sv * C57BL/6 * DBA/2 * SJL))
|
abnormal neuron differentiation
|
J:154650
|
Sox2tm3(TK)Hoch/Sox2+
(involves: 129S4/SvJae * C57BL/6)
|
decreased male germ cell number
|
J:177655
|
Sox2tm4.1Skn/Sox2tm4.1Skn Tg(Sox2-cre/ERT2)1Skn/0
(involves: 129S1/Sv * 129S4/SvJae)
|
abnormal neuron differentiation
|
J:154650
|
abnormal neuronal precursor proliferation
|
J:154650
|
abnormal radial glial cell morphology
|
J:154650
|
Sox3tm1.1Lja/Y
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased germ cell number
|
J:86431
|
oligozoospermia
|
J:86431
|
Sox3tm1.1Lja/Sox3tm1.1Lja
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal oocyte morphology
|
J:86431
|
Sox3tm1Pqt/Y
(chimera involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
cellular phenotype
|
J:195300
|
Sox4tm1Vlf/Sox4tm1Vlf Tg(Six3-cre)69Frty/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * DBA/2)
|
abnormal axon fasciculation
|
J:199663
|
increased retina apoptosis
|
J:199663
|
Sox8tm1Mkob/Sox8tm1Mkob
(involves: 129S7/SvEvBrd)
|
asthenozoospermia
|
J:136098
|
decreased elongated spermatid number
|
J:136098
|
Sox9em1(cre/ERT2)Tchn/Sox9+ Stk26tm2.1Zzh/Stk26tm2.1Zzh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal enterocyte proliferation
|
J:322311
|
Sox9tm1Gsr/Sox9tm1Gsr Shhtm1(EGFP/cre)Cjt/Shh+
(involves: 129P2/OlaHsd)
|
abnormal cell differentiation
|
J:202984
|
decreased cell migration
|
J:202984
|
decreased cell proliferation
|
J:202984
|
Sox9tm2Crm/Sox9tm2Crm Tg(Nr5a1-cre)5Asc/?
(involves: 129S7/SvEvBrd * C57BL/6 * CBA)
|
abnormal male meiosis
|
J:89368
|
Sox9tm2Crm/Sox9tm2Crm Tg(WT1-cre)1Asc/0
(involves: 129S7/SvEvBrd * C57BL/6 * CBA)
|
increased hair follicle apoptosis
|
J:100131
|
Sox9tm2Crm/Sox9tm2Crm Tg(Zp3-cre)93Knw/?
(involves: 129S7/SvEvBrd * C57BL/6J)
|
increased trunk neural crest cell apoptosis
|
J:105025
|
Sox9tm3(cre)Crm/Sox9+ Sp7tm1Crm/Sp7tm2Crm
(involves: 129S7/SvEvBrd * C57BL/6 * SJL)
|
abnormal osteoblast differentiation
|
J:102495
|
Sox10Dom/Sox10+
(involves: C3HeB/FeJLe * C57BL/6JLe)
|
abnormal neural crest cell migration
|
J:45117
|
Sox10Dom/Sox10+
(C57BL/6J-Sox10Dom)
|
abnormal neural crest cell physiology
|
J:165146
|
Sox10Dom/Sox10+
(C3Fe.B6JLe-Sox10Dom)
|
abnormal neural crest cell physiology
|
J:165146
|
Sox10Dom/Sox10+ Tg(DBHn-lacZ)8Rpk/0
(involves: C3HeB/FeJLe * C57BL/6JLe * SJL)
|
abnormal vagal neural crest cell migration
|
J:32868
|
Sox10Dom/Sox10Dom
(involves: C3HeB/FeJLe * C57BL/6JLe)
|
abnormal melanocyte differentiation
|
J:45117
|
abnormal neural crest cell migration
|
J:45117
|
Sox10tm1Weg/Sox10tm1Weg
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal axon fasciculation
|
J:203636
|
abnormal axon guidance
|
J:203636
|
decreased cell migration
|
J:203636
|
Sox10tm3(Sox8)Weg/Sox10tm3(Sox8)Weg
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal enteric neural crest cell migration
|
J:119015
|
increased vagal neural crest cell apoptosis
|
J:119015
|
Sox10tm4Weg/Sox10tm4Weg
(involves: 129P2/OlaHsd * C3H)
|
abnormal melanoblast migration
|
J:124679
|
Sox10tm5Weg/Sox10tm5Weg
(involves: 129P2/OlaHsd * C3H)
|
abnormal melanoblast migration
|
J:124679
|
Sox10tm7.1(Sox10)Weg/Sox10tm7.1(Sox10)Weg Tg(Dhh-cre)1Mejr/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL)
|
abnormal neuron proliferation
|
J:162692
|
increased neuron apoptosis
|
J:162692
|
Sox11tm1.1Gan/Sox11tm1.1Gan Sox4tm1Vlf/Sox4tm1Vlf Tg(Six3-cre)69Frty/0
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 * DBA/2)
|
increased retina apoptosis
|
J:199663
|
Sox11tm1.1Gan/Sox11tm1.1Gan Tg(Six3-cre)69Frty/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * DBA/2)
|
abnormal axon fasciculation
|
J:199663
|
increased retina apoptosis
|
J:199663
|
Sox11tm1.1Llei/Sox11tm1.1Llei Tg(Nes-cre/ERT2)73Lfp/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal neuron differentiation
|
J:198233
|
abnormal neuronal precursor proliferation
|
J:198233
|
Sox11tm1.2Llei/Sox11tm1.2Llei
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6)
|
abnormal neuron differentiation
|
J:198233
|
abnormal neuronal precursor proliferation
|
J:198233
|
increased neuron apoptosis
|
J:198233
|
Sox11tm1.2Vlf/Sox11tm1.2Vlf Sox4tm1.1Vlf/Sox4tm1.1Vlf
(involves: 129 * C57BL/6 * FVB/N)
|
abnormal cell death
|
J:175338
|
decreased cell proliferation
|
J:175338
|
Sox13tm1Jskg/Sox13tm1Jskg
(involves: C57BL/6)
|
increased T cell proliferation
|
J:117301
|
Sox15tm1Imad/Sox15tm1Imad
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal myoblast differentiation
|
J:93031
|
Sox17SHIVA/Sox17+
(either: C57BL/6-Sox17SHIVA or (involves: C57BL/6 * C3H/HeN))
|
abnormal peroxisome morphology
|
J:219119
|
Sox17tm2Sjm/Sox17tm2Sjm Tg(Cdh5-cre/ERT2)1Rha/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
decreased endothelial cell proliferation
|
J:234137
|
Sox30em1Laye/Sox30em1Laye
(C57BL/6J-Sox30em1Laye)
|
abnormal proacrosomal vesicle fusion
|
J:263980
|
abnormal spermatocyte morphology
|
J:263980
|
azoospermia
|
J:263980
|
decreased elongated spermatid number
|
J:263980
|
increased male germ cell apoptosis
|
J:263980
|
multinucleated giant male germ cells
|
J:263980
|
Sox30em2Hncs/Sox30em2Hncs
(involves: C57BL/6J * DBA * ICR)
|
increased male germ cell apoptosis
|
J:264140
|
Sox30tm1a(KOMP)Wtsi/Sox30tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal spermatid morphology
|
J:255310
|
azoospermia
|
J:255310
|
multinucleated giant male germ cells
|
J:255310
|
Sox30tm1c(KOMP)Wtsi/Sox30tm1c(KOMP)Wtsi Tg(Ddx4-cre)1Dcas/0
(involves: 129S4/SvJaeSor * C57BL/6N * FVB)
|
azoospermia
|
J:255310
|
multinucleated giant male germ cells
|
J:255310
|
Sp2tm1.1Htg/Sp2+ Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
decreased neuronal precursor proliferation
|
J:194076
|
Sp2tm1.1Htg/Sp2tm1.1Htg
(involves: 129)
|
abnormal cell cycle
|
J:194076
|
Sp2tm1.1Htg/Sp2tm1.1Htg Emx1tm1(cre)Krj/Emx1+
(involves: 129S2/SvPas)
|
abnormal neuron differentiation
|
J:194076
|
Sp2tm1.1Htg/Sp2tm1.1Htg Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
abnormal cell cycle
|
J:194076
|
abnormal neuron differentiation
|
J:194076
|
decreased neuronal precursor proliferation
|
J:194076
|
Sp2tm1.2Sus/Sp2tm1.2Sus
(involves: 129P2/OlaHsd * C57BL/6)
|
absent fibroblast proliferation
|
J:158671
|
Sp3tm1Sus/Sp3tm1Sus
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoblast differentiation
|
J:70829
|
Sp3tm2.1Sus/Sp3tm2.1Sus
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal DNA methylation
|
J:167521
|
Sp8tm2.1Aman/Sp8tm2.1Aman Foxg1tm1(cre)Skm/Foxg1+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal neuronal precursor proliferation
|
J:160653
|
increased neuron apoptosis
|
J:160653
|
Sp9tm1.1Zyan/Sp9tm1.1Zyan
(involves: 129S6/SvEvTac * C57BL/6J)
|
decreased neuronal precursor proliferation
|
J:238868
|
increased neuron apoptosis
|
J:238868
|
Sp9tm1.2Zyan/Sp9tm1.2Zyan Tg(Drd2-cre)ER43Gsat/0
(involves: 129S6/SvEvTac * C57BL/6J)
|
increased neuron apoptosis
|
J:238868
|
Spaca1tm1.1Osb/Spaca1tm1.1Osb
(involves: 129S2/SvPas * C57BL * C57BL/6N * DBA)
|
abnormal acrosome morphology
|
J:187685
|
abnormal sperm flagellum morphology
|
J:187685
|
abnormal sperm head morphology
|
J:187685
|
asthenozoospermia
|
J:187685
|
coiled sperm flagellum
|
J:187685
|
globozoospermia
|
J:187685
|
teratozoospermia
|
J:187685
|
Spaca1tm1.1Osb/Spaca1tm1.1Osb Tg(Acr-EGFP)1Osb/0
(involves: 129S2/SvPas * C3H * C57BL * C57BL/6 * DBA)
|
abnormal acrosome morphology
|
J:187685
|
abnormal spermatid morphology
|
J:187685
|
globozoospermia
|
J:187685
|
Spaca4em1Pauli/Spaca4em2Pauli
(C57BL/6J-Spaca4em1Pauli/Spaca4em2Pauli)
|
asthenozoospermia
|
J:311165
|
Spaca4tm1Osb/Spaca4tm1Osb
(involves: C57BL/6NSlc * DBA)
|
asthenozoospermia
|
J:311165
|
Spag4tm1(KOMP)Mbp/Spag4tm1(KOMP)Mbp
(involves: C57BL/6N)
|
abnormal manchette assembly
|
J:234041
|
abnormal manchette morphology
|
J:234041
|
abnormal sperm head morphology
|
J:234041
|
abnormal sperm nucleus morphology
|
J:234041
|
abnormal spermatid morphology
|
J:234041
|
absent manchette
|
J:234041
|
coiled sperm flagellum
|
J:234041
|
decreased elongated spermatid number
|
J:234041
|
detached acrosome
|
J:234041
|
globozoospermia
|
J:234041
|
Spag4tm1(KOMP)Mbp/Spag4tm1(KOMP)Mbp
(involves: C57BL/6J * C57BL/6N)
|
abnormal acrosome morphology
|
J:302087
|
abnormal manchette morphology
|
J:302087
|
abnormal outer dense fiber morphology
|
J:302087
|
abnormal sperm connecting piece morphology
|
J:302087
|
abnormal sperm nucleus morphology
|
J:302087
|
abnormal sperm principal piece morphology
|
J:302087
|
abnormal spermatid morphology
|
J:302087
|
decreased elongated spermatid number
|
J:302087
|
ectopic manchette
|
J:302087
|
globozoospermia
|
J:302087
|
oligozoospermia
|
J:302087
|
Spag6ltm1Jfs/Spag6l+
(involves: 129X1/SvJ * C57BL/6J)
|
asthenozoospermia
|
J:78433
|
Spag6ltm1Jfs/Spag6ltm1Jfs
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal outer dense fiber morphology
|
J:78433
|
abnormal sperm axoneme morphology
|
J:78433
|
abnormal sperm fibrous sheath morphology
|
J:78433
|
abnormal sperm flagellum morphology
|
J:78433
|
abnormal sperm midpiece morphology
|
J:78433
|
abnormal sperm principal piece morphology
|
J:78433
|
absent sperm axonemal central pair
|
J:78433
|
absent sperm head
|
J:78433
|
asthenozoospermia
|
J:78433
|
short sperm flagellum
|
J:78433
|
teratozoospermia
|
J:78433
|
Spag9m1Btlr/Spag9m1Btlr
(C57BL/6J-Spag9m1Btlr)
|
decreased activated sperm motility
|
J:159363
|
Spag9tm1Ysok/Spag9tm1Ysok
(involves: 129P2/OlaHsd * C57BL/6J)
|
asthenozoospermia
|
J:141755
|
oligozoospermia
|
J:141755
|
Spag16tm1Jfs/Spag16+
(chimera involves: 129/Sv * C57BL/6J)
|
abnormal outer dense fiber morphology
|
J:92446
|
abnormal sperm axoneme morphology
|
J:92446
|
abnormal sperm motility
|
J:92446
|
absent sperm axonemal central pair
|
J:92446
|
increased male germ cell apoptosis
|
J:92446
|
kinked sperm flagellum
|
J:92446
|
oligozoospermia
|
J:92446
|
Spag16tm2Jfs/Spag16tm2Jfs
(involves: 129S6/SvEvTac)
|
asthenozoospermia
|
J:107006
|
teratozoospermia
|
J:107006
|
Spag17tm1b(KOMP)Wtsi/Spag17tm1b(KOMP)Wtsi
(B6N(Cg)-Spag17tm1b(KOMP)Wtsi/J)
|
abnormal manchette assembly
|
J:264221
|
abnormal outer dense fiber morphology
|
J:264221
|
abnormal sperm axoneme morphology
|
J:264221
|
abnormal sperm head morphology
|
J:264221
|
abnormal sperm nucleus morphology
|
J:264221
|
absent sperm fibrous sheath
|
J:264221
|
absent sperm head
|
J:264221
|
detached acrosome
|
J:264221
|
elongated manchette
|
J:264221
|
immotile sperm
|
J:264221
|
oligozoospermia
|
J:264221
|
short sperm flagellum
|
J:264221
|
thin sperm flagellum
|
J:264221
|
Spag17tm1d(KOMP)Wtsi/Spag17tm1d(KOMP)Wtsi
(involves: 129S4/SvJaeSor * C57BL/6J * C57BL/6N)
|
abnormal respiratory motile cilium morphology
|
J:211752
|
abnormal respiratory motile cilium physiology
|
J:211752
|
immotile respiratory cilia
|
J:211752
|
Sparttm1.1Xen/Sparttm1.1Xen
(involves: C57BL/6J)
|
abnormal cell migration
|
J:185987
|
abnormal cell morphology
|
J:185987
|
abnormal mitosis
|
J:185987
|
increased cell nucleus count
|
J:185987
|
Spasttm1a(KOMP)Wtsi/Spasttm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal acrosome assembly
|
J:334562
|
abnormal acrosome morphology
|
J:334562
|
abnormal double-strand DNA break repair
|
J:334562
|
abnormal male meiosis
|
J:334562
|
abnormal manchette assembly
|
J:334562
|
abnormal manchette disassembly
|
J:334562
|
abnormal manchette morphology
|
J:334562
|
abnormal meiotic spindle morphology
|
J:334562
|
abnormal sperm nucleus morphology
|
J:334562
|
abnormal spermatid morphology
|
J:334562
|
aneuploidy
|
J:334562
|
arrest of male meiosis
|
J:334562
|
azoospermia
|
J:334562
|
ectopic manchette
|
J:334562
|
elongated manchette
|
J:334562
|
increased male germ cell apoptosis
|
J:334562
|
Spata2em1Jliu/Spata2em1Jliu
(involves: ICR)
|
abnormal spermatogonia morphology
|
J:247929
|
asthenozoospermia
|
J:247929
|
decreased male germ cell number
|
J:247929
|
oligozoospermia
|
J:247929
|
Spata2tm1(KOMP)Vlcg/Spata2tm1(KOMP)Vlcg
(C57BL/6-Spata2tm1(KOMP)Vlcg)
|
abnormal cell death
|
J:244164
|
Spata3em1Sbbx/Spata3em1Sbbx
(C57BL/6J-Spata3em1Sbbx)
|
detached acrosome
|
J:305339
|
teratozoospermia
|
J:305339
|
Spata6tm1a(KOMP)Wtsi/Spata6tm1a(KOMP)Wtsi
(B6J.B6N-Spata6tm1a(KOMP)Wtsi)
|
abnormal sperm annulus morphology
|
J:217662
|
abnormal sperm connecting piece morphology
|
J:217662
|
abnormal sperm end piece morphology
|
J:217662
|
abnormal sperm flagellum morphology
|
J:217662
|
abnormal sperm midpiece morphology
|
J:217662
|
abnormal spermatid morphology
|
J:217662
|
absent sperm head
|
J:217662
|
absent sperm mitochondrial sheath
|
J:217662
|
asthenozoospermia
|
J:217662
|
detached sperm flagellum
|
J:217662
|
oligozoospermia
|
J:217662
|
teratozoospermia
|
J:217662
|
Spata7tm1Mrd/Spata7tm1Mrd
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal photoreceptor connecting cilium morphology
|
J:264617
|
Spata16em2Osb/Spata16em2Osb
(involves: 129S2/SvPas * C57BL/6 * C57BL/6NSlc * DBA/2)
|
abnormal sperm flagellum morphology
|
J:258202
|
abnormal sperm head morphology
|
J:258202
|
oligozoospermia
|
J:258202
|
teratozoospermia
|
J:258202
|
Spata19tm1Lij/Spata19tm1Lij Tg(Stra8-icre)1Reb/0
(involves: 129S7/SvEvBrd * FVB/NJ)
|
abnormal respiratory electron transport chain
|
J:301706
|
abnormal sperm flagellum morphology
|
J:301706
|
abnormal sperm mitochondrial morphology
|
J:301706
|
abnormal sperm mitochondrial sheath morphology
|
J:301706
|
decreased sperm progressive motility
|
J:301706
|
Spata20Tn(pb-Act-RFP)1.1Zhu/Spata20Tn(pb-Act-RFP)1.1Zhu
(FVB/NJ-Spata20Tn(pb-Act-RFP)1.1Zhu)
|
abnormal manchette morphology
|
J:262160
|
abnormal manchette perinuclear ring morphology
|
J:262160
|
abnormal sperm flagellum morphology
|
J:262160
|
abnormal sperm head morphology
|
J:262160
|
asthenozoospermia
|
J:262160
|
decreased male germ cell number
|
J:262160
|
decreased sperm progressive motility
|
J:262160
|
decreased spermatid number
|
J:262160
|
oligozoospermia
|
J:262160
|
teratozoospermia
|
J:262160
|
Spata22repro42/Spata22repro42
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal double-strand DNA break repair
|
J:182054
|
abnormal female meiosis
|
J:182054
|
abnormal spermatocyte morphology
|
J:182054
|
absent oocytes
|
J:182054
|
arrest of male meiosis
|
J:182054
|
azoospermia
|
J:182054
|
decreased spermatid number
|
J:182054
|
Spata22repro42/Spata22repro42
(C3.B6-Spata22repro42)
|
decreased male germ cell number
|
J:249350
|
decreased oocyte number
|
J:249350
|
Spata22repro42/Spata22tm1a(KOMP)Wtsi
(involves: C3H * C57BL/6N)
|
absent oocytes
|
J:249350
|
arrest of male meiosis
|
J:249350
|
azoospermia
|
J:249350
|
decreased male germ cell number
|
J:249350
|
Spata22shani/Spata22shani
(C57BL/6J-Spata22shani)
|
abnormal chromosomal synapsis
|
J:297625
|
abnormal double-strand DNA break repair
|
J:297625
|
arrest of male meiosis
|
J:297625
|
increased male germ cell apoptosis
|
J:297625
|
Spata22tm1a(KOMP)Wtsi/Spata22tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal chromosomal synapsis
|
J:249350
|
abnormal double-strand DNA break repair
|
J:249350
|
abnormal female meiosis
|
J:249350
|
abnormal meiosis
|
J:249350
|
abnormal spermatid morphology
|
J:249350
|
abnormal spermatocyte morphology
|
J:249350
|
abnormal synaptonemal complex
|
J:249350
|
absent oocytes
|
J:249350
|
arrest of male meiosis
|
J:249350
|
azoospermia
|
J:249350
|
decreased male germ cell number
|
J:249350
|
Spata31tm1Yangy/Spata31tm1Yangy Tg(Ddx4-cre)1Dcas/0
(involves: 129S7/SvEvBrd * FVB)
|
decreased elongated spermatid number
|
J:301832
|
oligozoospermia
|
J:301832
|
teratozoospermia
|
J:301832
|
Spata33em1Osb/Spata33em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm midpiece morphology
|
J:309565
|
abnormal sperm motility
|
J:309565
|
Spata33em2Osb/Spata33em2Osb
(C57BL/6N-Spata33em2Osb/Osb)
|
abnormal sperm motility
|
J:309565
|
Spata46tm1Itl/Spata46tm1Itl
(involves: 129S6/SvEvTac * C57BL/6NTac)
|
abnormal acroplaxome morphology
|
J:236463
|
abnormal sperm head morphology
|
J:236463
|
abnormal sperm nucleus morphology
|
J:236463
|
abnormal spermatid morphology
|
J:236463
|
teratozoospermia
|
J:236463
|
Spatc1lem1Choc/Spatc1l+
(involves: C57BL/6J * C57BL/6N)
|
abnormal sperm head morphology
|
J:265193
|
absent sperm flagellum
|
J:265193
|
Spatc1lem1Choc/Spatc1lem1Choc
(involves: C57BL/6J * C57BL/6N)
|
absent sperm head
|
J:265193
|
detached sperm flagellum
|
J:265193
|
teratozoospermia
|
J:265193
|
Spdeftm1.2Cle/Spdeftm1.2Cle
(involves: 129P2/OlaHsd * FVB/N)
|
abnormal intestinal goblet cell morphology
|
J:154852
|
Spdyatm1.1Klad/Spdyatm1.1Klad
(involves: 129S1/Sv * C57BL/6J)
|
abnormal chiasmata formation
|
J:239544
|
abnormal chromosomal synapsis
|
J:239544
|
abnormal double-strand DNA break repair
|
J:239544
|
abnormal female meiosis
|
J:239544
|
abnormal male meiosis
|
J:239544
|
abnormal spermatocyte morphology
|
J:239544
|
abnormal synaptonemal complex
|
J:239544
|
abnormal telomere morphology
|
J:239544
|
arrest of male meiosis
|
J:239544
|
decreased elongated spermatid number
|
J:239544
|
decreased male germ cell number
|
J:239544
|
decreased oocyte number
|
J:239544
|
decreased round spermatid number
|
J:239544
|
decreased spermatid number
|
J:239544
|
Specc1lGt(DTM096)Byg/Specc1lGt(DTM096)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cranial neural crest cell migration
|
J:250140
|
abnormal neural crest cell delamination
|
J:250140
|
increased apoptosis
|
J:250140
|
Specc1lGt(DTM096)Byg/Specc1lGt(RRH048)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cranial neural crest cell migration
|
J:250140
|
abnormal neural crest cell delamination
|
J:250140
|
increased apoptosis
|
J:250140
|
Specc1lGt(RRH048)Byg/Specc1lGt(RRH048)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cranial neural crest cell migration
|
J:250140
|
abnormal neural crest cell delamination
|
J:250140
|
increased apoptosis
|
J:250140
|
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ Trmutm1Tomik/Trmutm1Tomik
(involves: C57BL/6 * DBA)
|
abnormal hepatocyte mitochondrial morphology
|
J:235644
|
abnormal mitochondrial crista morphology
|
J:235644
|
abnormal mitochondrial physiology
|
J:235644
|
abnormal tricarboxylic acid cycle
|
J:235644
|
increased cell nucleus count
|
J:235644
|
increased hepatocyte karyomegaly
|
J:235644
|
increased mitochondrial DNA content
|
J:235644
|
increased mitochondrial size
|
J:235644
|
Spef2bgh/Spef2bgh
(involves: C57BL/6J * C57BL/10J)
|
abnormal respiratory motile cilium physiology
|
J:176695
|
Spef2bgh/Spef2bgh
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J)
|
abnormal respiratory motile cilium physiology
|
J:176695
|
abnormal sperm axoneme morphology
|
J:176695
|
abnormal sperm fibrous sheath morphology
|
J:176695
|
abnormal sperm flagellum morphology
|
J:176695
|
abnormal sperm mitochondrial morphology
|
J:176695
|
oligozoospermia
|
J:176695
|
short sperm flagellum
|
J:176695
|
Spem1tm1Wyan/Spem1tm1Wyan
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal sperm head morphology
|
J:120937
|
asthenozoospermia
|
J:120937
|
teratozoospermia
|
J:120937
|
Spem2em1Smoc/Spem2em1Smoc
(C57BL/6JSmoc-Spem2em1Smoc/Smoc)
|
abnormal acrosome assembly
|
J:354200
|
abnormal acrosome morphology
|
J:354200
|
abnormal sperm head morphology
|
J:354200
|
abnormal sperm midpiece morphology
|
J:354200
|
abnormal sperm mitochondrial morphology
|
J:354200
|
abnormal sperm nucleus morphology
|
J:354200
|
abnormal spermatid morphology
|
J:354200
|
asthenozoospermia
|
J:354200
|
disorganized sperm mitochondrial sheath
|
J:354200
|
impaired sperm migration in female genital tract
|
J:354200
|
multi-headed sperm
|
J:354200
|
multiflagellated sperm
|
J:354200
|
oligozoospermia
|
J:354200
|
teratozoospermia
|
J:354200
|
Spesp1tm1Osb/Spesp1tm1Osb
(involves: 129S2/SvPas * C57BL/6)
|
abnormal acrosome morphology
|
J:159611
|
Spg11Gt(EUCE0085f05)Hmgu/Spg11Gt(EUCE0085f05)Hmgu
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal autophagy
|
J:228803
|
abnormal lysosome morphology
|
J:228803
|
abnormal lysosome physiology
|
J:228803
|
Spg21tm1Mchan/Spg21tm1Mchan
(Not Specified)
|
abnormal neuron differentiation
|
J:302080
|
Spha1MSM/Ms/Spha1MSM/Ms
(involves: C57BL/6J * MSM/Ms)
|
abnormal sperm head morphology
|
J:88875
|
Spha2MSM/Ms/Spha2MSM/Ms
(involves: C57BL/6J * MSM/Ms)
|
abnormal sperm head morphology
|
J:88875
|
Spha3MSM/Ms/Spha3MSM/Ms
(involves: C57BL/6J * MSM/Ms)
|
abnormal sperm head morphology
|
J:88875
|
Sphk1tm1Rlp/Sphk1tm1Rlp Sphk2tm1Rlp/Sphk2tm1Rlp
(involves: 129S6/SvEvTac * C57BL/6)
|
increased embryonic neuroepithelium apoptosis
|
J:103755
|
increased hindbrain apoptosis
|
J:103755
|
increased midbrain apoptosis
|
J:103755
|
Sphk2tm1Npa/Sphk2tm1Npa
(BALB/c-Sphk2tm1Npa)
|
abnormal B cell migration
|
J:129314
|
Spi1tm1.2Nutt/Spi1tm1.2Nutt Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
abnormal granulocyte differentiation
|
J:98188
|
Spi1tm1.3Dgt/Spi1tm1.3Dgt
(involves: 129 * BALB/c * C57BL/6)
|
abnormal chromosome number
|
J:90331
|
Spi1tm1Ram/Spi1tm1Ram
(involves: 129S2/SvPas * C57BL/6)
|
abnormal macrophage differentiation
|
J:36473
|
abnormal neutrophil differentiation
|
J:36473
|
Spi1tm1Sing/Spi1+ Spibtm1Mcs/Spib+
(involves: 129S/SvEv * 129X1/SvJ)
|
decreased B cell proliferation
|
J:88257
|
Spi1tm1Sing/Spi1+ Spibtm1Mcs/Spibtm1Mcs
(involves: 129S/SvEv * 129X1/SvJ)
|
decreased B cell proliferation
|
J:88257
|
increased B cell apoptosis
|
J:88257
|
Spi1tm4.1Dgt/Spi1tm4.1Dgt
(B6.129(Cg)-Spi1tm4.1Dgt)
|
abnormal cell cycle
|
J:196609
|
increased hematopoietic stem cell proliferation
|
J:196609
|
Spibtm1Mcs/Spibtm1Mcs
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased B cell proliferation
|
J:88257
|
Spibtm1Mcs/Spibtm1Mcs
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased B cell proliferation
|
J:45245
|
increased B cell apoptosis
|
J:45245
|
Spictm1.1Kmm/Spictm1.1Kmm
(involves: 129S6/SvEvTac * C57BL/6)
|
impaired macrophage phagocytosis
|
J:143900
|
Spictm1Kmm/Spictm1Kmm
(involves: 129S6/SvEvTac * C57BL/6)
|
impaired macrophage phagocytosis
|
J:143900
|
Spin1Gt(RRZ449)Byg/Spin1Gt(RRZ449)Byg
(B6.129P2-Spin1Gt(RRZ449)Byg)
|
abnormal female meiosis I arrest
|
J:204704
|
Spin4em1Jbn/Y
(involves: C57BL/6J)
|
increased chondrocyte proliferation
|
J:347154
|
Spin4em2Jbn/Y
(involves: C57BL/6J)
|
increased chondrocyte proliferation
|
J:347154
|
Spindocem1Mtb/Spindocem1Mtb
(FVB-Spindocem1Mtb)
|
increased cellular sensitivity to X-ray irradiation
|
J:319478
|
Spindocem2Mtb/Spindocem2Mtb
(FVB-Spindocem2Mtb)
|
increased cellular sensitivity to X-ray irradiation
|
J:319478
|
Spink2Gt(327A6)Cmhd/Spink2Gt(327A6)Cmhd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:175913
|
kinked sperm flagellum
|
J:175913
|
oligozoospermia
|
J:175913
|
teratozoospermia
|
J:175913
|
Spint1Gt(OST380474)Lex/Spint1Gt(OST380474)Lex
(involves: 129S5/SvEvBrd)
|
abnormal basement membrane morphology
|
J:118798
|
Spint1tm1Hk/Spint1tm1Hk
(involves: C57BL/6 * CBA)
|
increased embryonic tissue cell apoptosis
|
J:99182
|
Spint1tm2.1Hk/Spint1tm2.1Hk Tg(Vil1-cre)997Gum/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
abnormal enterocyte proliferation
|
J:179937
|
increased enterocyte apoptosis
|
J:179937
|
Spmap2Tg(PDE5A)1Ynk/Spmap2Tg(PDE5A)1Ynk
(involves: C3H)
|
abnormal sperm axoneme morphology
|
J:62271
|
abnormal sperm flagellum morphology
|
J:62271
|
abnormal sperm nucleus morphology
|
J:62271
|
abnormal spermatid morphology
|
J:62271
|
absent sperm flagellum
|
J:62271
|
asthenozoospermia
|
J:62271
|
azoospermia
|
J:62271
|
decreased male germ cell number
|
J:62271
|
teratozoospermia
|
J:62271
|
Spmd1Smt/Spmd1Smt
(involves: M. m. molossinus * Smt)
|
abnormal male meiosis
|
J:108418
|
multinucleated giant male germ cells
|
J:108418
|
Spmd2M. m. molossinus/Spmd2Smt
(involves: M. m. molossinus * Smt)
|
oligozoospermia
|
J:108418
|
Spmd2Smt/Spmd2Smt
(involves: M. m. molossinus * Smt)
|
oligozoospermia
|
J:108418
|
Spmd2Smt/Spmd2Smt Spmd4Smt/Spmd4Smt
(involves: M. m. molossinus * Smt)
|
oligozoospermia
|
J:108418
|
Spmd3Smt/Spmd3Smt
(involves: M. m. molossinus * Smt)
|
oligozoospermia
|
J:108418
|
Spmd4Smt/Spmd4Smt
(involves: M. m. molossinus * Smt)
|
abnormal male meiosis
|
J:108418
|
Spmip7tm1Itl/Spmip7tm1Itl
(involves: C57BL/6J)
|
azoospermia
|
J:301738
|
Spmip10em1Osb/Spmip10em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm motility
|
J:309565
|
Spntm1Bam/Spntm1Bam
(involves: 129S4/SvJae * C57BL/6)
|
increased T cell proliferation
|
J:29272,
J:88252
|
Spo11tm1.1Gvpc/Spo11tm1.1Gvpc
(involves: C57BL/6)
|
abnormal double-strand DNA break repair
|
J:202231
|
Spo11tm1.1Gvpc/Spo11tm3Rdco
(involves: C57BL/6)
|
abnormal double-strand DNA break repair
|
J:202231
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:202231
|
arrest of male meiosis
|
J:202231
|
azoospermia
|
J:202231
|
Spo11tm1Bdm/Spo11tm1Bdm
(involves: 129)
|
abnormal double-strand DNA break repair
|
J:199075
|
abnormal meiosis
|
J:199075
|
abnormal oogenesis
|
J:199075
|
abnormal synaptonemal complex
|
J:199075
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:199075
|
Spo11tm1Mjn/Spo11+
(B6.Cg-Spo11tm1Mjn)
|
abnormal double-strand DNA break repair
|
J:280261
|
Spo11tm1Mjn/Spo11+ Stag3tm1e.1(KOMP)Wtsi/Stag3tm1e.1(KOMP)Wtsi
(B6.Cg-Spo11tm1Mjn Stag3tm1e.1(KOMP)Wtsi/2J)
|
abnormal double-strand DNA break repair
|
J:280261
|
Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * C57BL/6)
|
abnormal female meiosis
|
J:65880
|
abnormal male meiosis
|
J:65880
|
abnormal oogenesis
|
J:65880
|
azoospermia
|
J:65880
|
decreased oocyte number
|
J:65880
|
decreased spermatid number
|
J:65880
|
Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * C57BL/6JOlaHsd)
|
abnormal female meiosis
|
J:173089
|
decreased oocyte number
|
J:173089
|
increased female germ cell apoptosis
|
J:173089
|
Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ)
|
abnormal female meiosis
|
J:192634
|
abnormal meiosis
|
J:183982
|
abnormal synaptonemal complex
|
J:236226
|
decreased oocyte number
|
J:192634,
J:183982
|
Spo11tm1Mjn/Spo11tm1Mjn
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal chromosomal synapsis
|
J:209347
|
abnormal double-strand DNA break repair
|
J:209347
|
abnormal male meiosis
|
J:187173,
J:209347
|
arrest of male meiosis
|
J:209347
|
Spo11tm1Nki/Spo11tm1Nki
(involves: 129P2/OlaHsd)
|
abnormal female meiosis
|
J:177475
|
abnormal male meiosis
|
J:177475
|
abnormal meiosis
|
J:177475
|
abnormal synaptonemal complex
|
J:177475
|
Spo11tm1Rdco/Spo11tm1Rdco
(involves: 129S6/SvEvTac)
|
abnormal female meiosis
|
J:65881
|
abnormal male meiosis
|
J:194067
|
arrest of male meiosis
|
J:65881
|
Spo11tm1Rdco/Spo11tm1Rdco
(involves: 129 * C57BL/6)
|
arrest of male meiosis
|
J:140402
|
Spo11tm2.1Rdco/Spo11tm2.1Rdco
(B6.129S6-Spo11tm2.1Rdco)
|
abnormal male meiosis
|
J:194067
|
arrest of male meiosis
|
J:194067
|
Spocd1em1Doca/Spocd1em1Doca
(involves: C57BL/6 * C57BL/6N * CBA)
|
abnormal chromosomal synapsis
|
J:295943
|
abnormal DNA methylation during gametogenesis
|
J:295943
|
azoospermia
|
J:295943
|
increased testis apoptosis
|
J:295943
|
SpopGt(BGB118)Byg/Spop+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal pancreatic islet cell apoptosis
|
J:165268
|
Spout1tm1Mxu/Spout1+
(involves: 129 * C57BL/6)
|
abnormal male germ cell apoptosis
|
J:88144
|
decreased sensitivity to induced cell death
|
J:88144
|
Spout1tm1Mxu/Spout1+ Dffatm1Mxu/Dffatm1Mxu
(involves: 129 * C57BL/6)
|
decreased apoptosis
|
J:88144
|
Spp1tm1Blh/Spp1+
(involves: 129S6/SvEvTac * Black Swiss)
|
abnormal leukocyte migration
|
J:86531
|
Spp1tm1Blh/Spp1tm1Blh
(involves: 129S6/SvEvTac * Black Swiss)
|
abnormal leukocyte migration
|
J:86531
|
abnormal macrophage chemotaxis
|
J:140014
|
Spp1tm1Blh/Spp1tm1Blh
(B6.129S6-Spp1tm1Blh)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:118432
|
Spp1tm1Blh/Spp1tm1Blh
(BKSW.129S6-Spp1tm1Blh)
|
impaired macrophage chemotaxis
|
J:113585
|
Spp1tm1Rit/Spp1tm1Rit
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal osteoblast physiology
|
J:128077
|
decreased fibroblast chemotaxis
|
J:106243
|
decreased sensitivity to induced cell death
|
J:95591
|
Sppl2achompB/Sppl2achompB
(involves: C57BL/6)
|
decreased activation-induced B cell apoptosis
|
J:194595
|
decreased B cell proliferation
|
J:194595
|
Sppl2ctm1.1(KOMP)Vlcg/Sppl2ctm1.1(KOMP)Vlcg
(involves: C57BL/6NCrl * C57BL/6NTac)
|
asthenozoospermia
|
J:272982
|
decreased elongated spermatid number
|
J:272982
|
Sppl2ctm1.1(KOMP)Vlcg/Sppl2ctm1.1(KOMP)Vlcg
(C57BL/6NTac-Sppl2ctm1.1(KOMP)Vlcg)
|
asthenozoospermia
|
J:328498
|
sprawl/sprawl Tg(Mbp-MAPT/lacZ)#aCaw/Tg(Mbp-MAPT/lacZ)#aCaw
(involves: BALB/c * C57BL/6 * C57BL/6J * FVB/N)
|
abnormal axon fasciculation
|
J:168258
|
Spred1tm1.1Ayos/Spred1tm1.1Ayos
(involves: 129 * C57BL/6 * SJL)
|
increased mast cell degranulation
|
J:186742
|
Sprnem1Jvt/Sprnem1Jvt
(FVB/NJ-Sprnem1Jvt)
|
decreased mammary gland epithelial cell proliferation
|
J:289583
|
maternal effect
|
J:289583
|
Sprr2fem1Jadb/Sprr2fem1Jadb
(C57BL/6-Sprr2fem1Jadb)
|
increased cellular sensitivity to oxidative stress
|
J:299874
|
Sprtntm1.2Yjm/Sprtntm1.2Yjm
(involves: 129S/SvEv * C57BL/6)
|
decreased inner cell mass proliferation
|
J:225198
|
Sprtntm1Yjm/Sprtntm1.2Yjm
(involves: 129S/SvEv * C57BL/6)
|
abnormal cell nucleus morphology
|
J:225198
|
chromosomal instability
|
J:225198
|
decreased fibroblast proliferation
|
J:225198
|
Sprtntm1Yjm/Sprtntm1Yjm
(involves: 129S/SvEv * C57BL/6)
|
chromosomal instability
|
J:225198
|
early cellular replicative senescence
|
J:225198
|
Spry2tm1.1Mrt/Spry2+ Spry4tm1.2Mrt/Spry4tm1.2Mrt
(involves: 129P2/OlaHsd)
|
abnormal primary cilium morphology
|
J:315670
|
Spry2tm1.1Mrt/Spry2tm1.1Mrt
(involves: 129P2/OlaHsd)
|
abnormal primary cilium morphology
|
J:315670
|
Spta1sph-ha/Spta1sph-ha
(either: (B6.D1-Spta1sph-ha x WB.D1-Spta1sph-ha)F1 or (WB.D1-Spta1sph-ha x B6.D1-Spta1sph-ha)F1)
|
increased B cell proliferation
|
J:1967
|
increased T cell proliferation
|
J:1967
|
Sptan1Gt(RRQ171)Byg/Sptan1Gt(RRQ171)Byg
(B6.129P2-Sptan1Gt(RRQ171)Byg)
|
abnormal cell physiology
|
J:186305
|
increased cell proliferation
|
J:186305
|
Sptan1tm1.1Gnic/Sptan1tm1.1Gnic
(either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6))
|
cellular phenotype
|
J:122549
|
Sptbn1tm1a(EUCOMM)Wtsi/Sptbn1tm1a(EUCOMM)Wtsi
(involves: C57BL/6N)
|
decreased fetal cardiomyocyte proliferation
|
J:219548
|
decreased mitotic index
|
J:219548
|
increased fetal cardiomyocyte apoptosis
|
J:219548
|
Sptbn1tm1c(EUCOMM)Wtsi/Sptbn1tm1c(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal cell cycle
|
J:219548
|
abnormal cell cycle checkpoint function
|
J:219548
|
decreased fetal cardiomyocyte proliferation
|
J:219548
|
increased fetal cardiomyocyte apoptosis
|
J:219548
|
Sptbn1tm1Mish/Sptbn1+
(involves: 129S6/SvEvTac * C57BL/6)
|
decreased hepatocyte proliferation
|
J:132133
|
Sptlc2tm1Yhir/Sptlc2tm1Yhir Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: C57BL/6 * C57BL/6NTac)
|
cellular necrosis
|
J:202954
|
Sptlc2tm2.1Jia/Sptlc2tm2.1Jia
(involves: 129S4/SvJaeSor * C57BL/6)
|
increased cholesterol efflux
|
J:155507
|
SptssbTvrm122/SptssbTvrm122
(involves: A * C57BL/6)
|
abnormal endoplasmic reticulum stress
|
J:224971
|
Sqstm1tm1.1Sral/Sqstm1+
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:173755
|
Sqstm1tm1.1Sral/Sqstm1tm1.1Sral
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:173755
|
Sqstm1tm1Hwl/Sqstm1tm1Hwl
(B6.129P2-Sqstm1tm1Hwl)
|
abnormal mitochondrial physiology
|
J:181228
|
abnormal respiratory electron transport chain
|
J:181228
|
oxidative stress
|
J:181228
|
Sqstm1tm1Jjw/Sqstm1tm1Jjw
(involves: 129 * C57BL/6)
|
abnormal osteoclast differentiation
|
J:141179
|
Sqstm1tm1Jmos/Sqstm1tm1Jmos
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal osteoclast differentiation
|
J:90010
|
Sqstm1tm1Jmos/Sqstm1tm1Jmos
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal aerobic respiration
|
J:194291
|
Sqstm1tm1Keta/Sqstm1tm1Keta
(involves: 129 * C57BL/6N)
|
abnormal osteoblast physiology
|
J:264183
|
abnormal osteoclast differentiation
|
J:264183
|
Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos Lyz2tm1(cre)Ifo/Lyz2+
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:194291
|
Sqstm1tm2.1Jmos/Sqstm1tm2.1Jmos Tg(Fabp4-cre)1Rev/0
(Not Specified)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:194291
|
abnormal mitochondrial crista morphology
|
J:194291
|
disorganized mitochondrial cristae
|
J:194291
|
Srctm1Mul/Srctm1Mul Tg(MMTV-PyVT)#Mul/0
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
decreased cell proliferation
|
J:181822
|
increased apoptosis
|
J:181822
|
Srftm1Rjs/Srftm2.1Nor Tg(Myh6-cre)2182Mds/0
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:101311
|
Srftm1Zli/Srftm1Zli Tg(Myh7-cre)1Zli/0
(involves: 129/Sv * C57BL/6)
|
abnormal apoptosis
|
J:91025
|
Srgap1tm1a(KOMP)Wtsi/Srgap1tm1a(KOMP)Wtsi Six2tm1(tTA,tetO-EGFP/cre)Amc/Six2+
(involves: 129 * C57BL/6J * C57BL/6N)
|
detached podocyte
|
J:333727
|
increased mesangial cell number
|
J:333727
|
Srgap1tm1a(KOMP)Wtsi/Srgap1tm1a(KOMP)Wtsi Tg(NPHS2-cre)295Lbh/0
(involves: C57BL/6 * C57BL/6N * SJL)
|
increased mesangial cell number
|
J:333727
|
Srpk1tm1Xdfu/Srpk1tm1Xdfu
(involves: 129)
|
decreased cell proliferation
|
J:213142
|
early cellular replicative senescence
|
J:213142
|
Srrtm1(cre/PGR)Himo/Srrtm1(cre/PGR)Himo
(C57BL/6N-Srrtm1(cre/PGR)Himo)
|
decreased susceptibility to neuronal excitotoxicity
|
J:144030
|
Srrm4tm1b(EUCOMM)Wtsi/Srrm4+
(involves: C57BL/6J * C57BL/6N)
|
abnormal axon guidance
|
J:221584
|
Srrm4tm1b(EUCOMM)Wtsi/Srrm4tm1b(EUCOMM)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal axon extension
|
J:221584
|
abnormal axon guidance
|
J:221584
|
premature neuronal precursor differentiation
|
J:221584
|
Srrttm1.1Thsn/Srrttm1.2Thsn Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA)
|
increased splenocyte apoptosis
|
J:152729
|
Srrttm1Bfk/Srrttm1Bfk
(either: (involves: 129S1/Sv * 129S2/SvPasCrl * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * Crl:CD-1))
|
increased embryonic tissue cell apoptosis
|
J:132672
|
Srsf1tm1Xdfu/Srsf1tm1Xdfu Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
(involves: 129S4/SvJae * C57BL/6 * SJL)
|
increased retina apoptosis
|
J:143205
|
Srsf2tm1.1Oaw/Srsf2+ Tg(Mx1-cre)1Cgn/?
(B6.Cg-Tg(Mx1-cre)1Cgn Srsf2tm1.1Oaw)
|
abnormal cell cycle
|
J:221404
|
increased apoptosis
|
J:221404
|
Srsf3tm1Pjln/Srsf3tm1Pjln Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: BALB/c * C57BL/6 * DBA)
|
abnormal endoplasmic reticulum morphology
|
J:205756
|
decreased fatty acid oxidation
|
J:205756
|
increased hepatocyte apoptosis
|
J:205756
|
Srsf5em1Nju/Srsf5em1Nju
(C57BL/6JGpt-Srsf5em1Nju)
|
decreased fetal cardiomyocyte proliferation
|
J:311867
|
Ssbp3Tg(SOD1)1Hssk/Ssbp3Tg(SOD1)1Hssk
(involves: C3H/He * C57BL/6)
|
decreased cell proliferation
|
J:98485
|
increased apoptosis
|
J:98485
|
Ssmem1em1Osb/Ssmem1em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal sperm head morphology
|
J:296963
|
asthenozoospermia
|
J:296963
|
globozoospermia
|
J:296963
|
Ssr3tm1Ryn/Ssr3tm1Ryn
(involves: C57BL/6 * CBA)
|
increased placenta apoptosis
|
J:167832
|
Sstr1tm1Dric/Sstr1tm1Dric
(involves: 129S4/SvJae)
|
abnormal retina apoptosis
|
J:122896
|
Ssu72tm1Cwl/Ssu72tm1Cwl Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(B6.Cg-Ssu72tm1Cwl Speer6-ps1Tg(Alb-cre)21Mgn)
|
increased hepatocyte apoptosis
|
J:309624
|
increased hepatocyte karyomegaly
|
J:309624
|
increased hepatocyte proliferation
|
J:309624
|
St3gal2tm1Jxm/St3gal2tm1Jxm
(Not Specified)
|
decreased T cell proliferation
|
J:217719
|
St3gal4tm1.1Jxm/St3gal4tm1.1Jxm
(B6.129-St3gal4tm1.1Jxm)
|
abnormal leukocyte tethering or rolling
|
J:117085
|
St3gal4tm1.1Jxm/St3gal4tm1.1Jxm
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal leukocyte migration
|
J:189086
|
St3gal4tm1.1Jxm/St3gal4tm1.1Jxm St3gal6tm1.1Jxm/St3gal6tm1.1Jxm
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal leukocyte migration
|
J:189086
|
impaired leukocyte tethering or rolling
|
J:189086
|
St3gal6tm1.1Jxm/St3gal6tm1.1Jxm
(B6.Cg-St3gal6tm1.1Jxm)
|
impaired leukocyte tethering or rolling
|
J:189086
|
St6galnac2tm1.1Cfg/St6galnac2tm1.1Cfg
(involves: 129S1/Sv * 129X1/SvJ)
|
increased B cell proliferation
|
J:217719
|
St8sia1tm1Kfk/St8sia1tm1Kfk
(Not Specified)
|
increased T cell proliferation
|
J:73818
|
St8sia2tm1Jxm/St8sia2tm1Jxm St8sia4tm1.1Mifu/St8sia4tm1.1Mifu
(involves: C57BL/6)
|
abnormal neuron differentiation
|
J:126687
|
impaired neuronal migration
|
J:126687
|
increased neuron apoptosis
|
J:126687
|
St14tm1Bug/St14tm1Bug
(involves: 129P2/OlaHsd * Black Swiss)
|
increased thymocyte apoptosis
|
J:87125
|
St14tm1Bug/St14tm1Bug
(involves: 129P2/OlaHsd)
|
abnormal keratinocyte differentiation
|
J:86715
|
St14tm2Bug/St14tm2Bug
(involves: 129P2/OlaHsd)
|
abnormal keratinocyte differentiation
|
J:86715
|
St14tm2Bug/St14tm3Bug Tg(Vil1-cre)997Gum/0
(involves: 129P2/OlaHsd * 129S6/SvEvTac * Black Swiss * C57BL/6 * SJL)
|
abnormal enterocyte proliferation
|
J:153070
|
Stag1Gt(P099A04)Wrst/Stag1+
(involves: 129S2/SvPas)
|
abnormal mitosis
|
J:184720
|
abnormal telomere morphology
|
J:184720
|
decreased cell proliferation
|
J:184720
|
Stag1Gt(P099A04)Wrst/Stag1Gt(P099A04)Wrst
(involves: 129S2/SvPas)
|
abnormal mitosis
|
J:184720
|
abnormal telomere morphology
|
J:184720
|
aneuploidy
|
J:184720
|
decreased cell proliferation
|
J:184720
|
decreased fibroblast proliferation
|
J:184720
|
Stag2tm1.1Alos/Y Tg(CAG-cre)1Nagy/0
(involves: 129S6/SvEvTac * C57BL/6NCrl)
|
decreased cell proliferation
|
J:298088
|
Stag3TgTn(sb-cHS4,Tyr)2312COve/Stag3TgTn(sb-cHS4,Tyr)2312COve
(FVB/N-Stag3TgTn(sb-cHS4,Tyr)2312COve)
|
absent oocytes
|
J:175597
|
azoospermia
|
J:175597
|
Stag3tm1e.1(KOMP)Wtsi/Stag3tm1e.1(KOMP)Wtsi
(B6N(Cg)-Stag3tm1e.1(KOMP)Wtsi)
|
abnormal chromosomal synapsis
|
J:280261
|
abnormal double-strand DNA break repair
|
J:280261
|
abnormal male meiosis
|
J:280261
|
abnormal synaptonemal complex
|
J:280261
|
increased male germ cell apoptosis
|
J:280261
|
Stamtm2Sug/Stamtm2Sug Stam2tm1Sug/Stam2tm1Sug Tg(Lck-cre)I57Jxm/0
(involves: 129S4/SvJae * C57BL/6 * ICR)
|
decreased T cell proliferation
|
J:80617
|
Stard13tm1Ioln/Stard13tm1Ioln
(B6.129S7-Stard13tm1Ioln)
|
cellular phenotype
|
J:152475
|
Stat1m2Btlr/Stat1m2Btlr
(C57BL/6J-Stat1m2Btlr)
|
decreased NK cell degranulation
|
J:134096
|
Stat1tm1Rds/Stat1tm1Rds
(either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6))
|
abnormal cell physiology
|
J:31326
|
Stat1tm1Rds/Stat1tm1Rds
(involves: 129)
|
abnormal cell cycle
|
J:109408
|
decreased sensitivity to induced cell death
|
J:62316
|
Stat1tm1Rds/Stat1tm1Rds
(129S6/SvEv-Stat1tm1Rds/Tac)
|
abnormal osteoclast differentiation
|
J:131353
|
abnormal redox activity
|
J:122801
|
decreased hepatocyte apoptosis
|
J:122801
|
decreased susceptibility to neuronal excitotoxicity
|
J:116659
|
increased cardiomyocyte apoptosis
|
J:120449
|
Stat1tm1Rds/Stat1tm1Rds
(B6.129-Stat1tm1Rds)
|
abnormal osteoblast differentiation
|
J:84894
|
Stat3tm1Aki/Stat3tm1Aki
(involves: 129P2/OlaHsd)
|
decreased inner cell mass proliferation
|
J:40106
|
Stat3tm1Dnl/Stat3tm1Dlv
(involves: C57BL/6)
|
increased thymocyte apoptosis
|
J:87599
|
Stat3tm1Vpo/Stat3tm1Vpo Tg(Myh6-cre)2182Mds/0
(involves: 129P2/OlaHsd * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:141591
|
oxidative stress
|
J:141591
|
Stat3tm1Xyfu/Stat3tm1.1Xyfu Tg(Myh6-cre)2182Mds/0
(involves: 129S1/Sv * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:86400
|
Stat3tm1Xyfu/Stat3tm1.1Xyfu Tg(Ttr-cre)10-3Xyfu/?
(involves: 129S1/Sv * C57BL/6)
|
decreased hepatocyte proliferation
|
J:128719
|
Stat3tm2Aki/Stat3tm2Aki Tg(KRT5-cre)1Tak/0
(involves: 129P2/OlaHsd * C3H * C57BL/6)
|
decreased keratinocyte migration
|
J:65302
|
Stat3tm2Aki/Stat3tm2Aki Tg(KRT5-cre/ERT2)AJdg/0
(involves: 129P2/OlaHsd * FVB/N)
|
increased apoptosis
|
J:138529
|
Stat3tm2Aki/Stat3tm2Aki Tg(Lck-cre)1Jtak/0
(involves: 129P2/OlaHsd)
|
decreased T cell proliferation
|
J:50443
|
increased T cell apoptosis
|
J:50443
|
Stat3tm4Vpo/Stat3tm4Vpo Tg(MMTV-Erbb2)1Pv/0
(involves: 129P2/OlaHsd * BALB/cAn * C57BL/6 * CD-1 * DBA)
|
abnormal actin cytoskeleton morphology
|
J:157976
|
abnormal cell adhesion
|
J:157976
|
abnormal cell migration
|
J:157976
|
decreased apoptosis
|
J:157976
|
Stat4tm1Gru/Stat4tm1Gru
(involves: 129S2/SvPas * BALB/c)
|
abnormal T cell proliferation
|
J:34059
|
Stat5atm1.1Wjl/Stat5atm1.1Wjl Stat5btm2.1Wjl/Stat5btm2.1Wjl
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N)
|
decreased T cell proliferation
|
J:187325
|
increased T cell apoptosis
|
J:187325
|
Stat5atm1Jni/Stat5atm1Jni Stat5btm2Jni/Stat5btm2Jni
(involves: 129 * C57BL/6)
|
abnormal mast cell differentiation
|
J:84889
|
Stat5atm1Mam/Stat5atm1Mam
(C.129S6-Stat5atm1Mam)
|
abnormal mast cell differentiation
|
J:101855
|
Stat5atm2Mam/Stat5atm2Mam Stat5btm1Mam/Stat5btm1Mam Tg(Mx1-cre)1Cgn/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal neutrophil differentiation
|
J:155489
|
decreased cell proliferation
|
J:155489
|
increased apoptosis
|
J:155489
|
Stat5atm2Mam/Stat5atm2Mam Stat5btm1Mam/Stat5btm1Mam Tg(Tek-cre)1Ywa/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased apoptosis
|
J:138904
|
Stat5atm2Mam/Stat5atm2Mam Tg(Ins2-cre)23Herr/0
(involves: 129S6/SvEvTac * C57BL/6J * CBA/J)
|
decreased pancreatic beta cell proliferation
|
J:284574
|
Stat5btm1Hwd/Stat5btm1Hwd
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:112035
|
Stat5btm1Mam/Stat5btm1Mam Tg(Mx1-cre)1Cgn/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal neutrophil differentiation
|
J:155489
|
decreased cell proliferation
|
J:155489
|
increased apoptosis
|
J:155489
|
Stat5btm1Mam/Stat5btm1Mam Tg(Tek-cre)1Ywa/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
increased apoptosis
|
J:138904
|
Stat6tm1Aki/Stat6tm1Aki
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:32561
|
decreased T cell proliferation
|
J:32561
|
Stat6tm1Gru/Stat6tm1Gru
(129S2/SvPas-Stat6tm1Gru)
|
decreased T cell proliferation
|
J:31932
|
Stat6tm1Gru/Stat6tm1Gru
(involves: 129S2/SvPas)
|
decreased mammary gland epithelial cell proliferation
|
J:184505
|
Stat6tm1Gru/Stat6tm1Gru
(involves: 129S2/SvPas * BALB/c)
|
impaired eosinophil chemotaxis
|
J:85386
|
impaired neutrophil chemotaxis
|
J:85386
|
Stat6tm1Gru/Stat6tm1Gru
(C.129S2-Stat6tm1Gru)
|
abnormal leukocyte migration
|
J:74497
|
Stat6tm1Jni/Stat6tm1Jni
(involves: 129S/SvEv)
|
abnormal B cell proliferation
|
J:32607
|
increased B cell apoptosis
|
J:146533
|
increased cellular sensitivity to gamma-irradiation
|
J:146533
|
Stc2tm1Gthi/Stc2tm1Gthi
(involves: 129S/SvEv * C57BL/6)
|
abnormal cell physiology
|
J:175075
|
increased cellular sensitivity to hydrogen peroxide
|
J:175075
|
increased sensitivity to induced cell death
|
J:175075
|
Steap3tm1.1Atel/Steap3tm1.1Atel
(involves: C57BL/6)
|
abnormal vesicle-mediated transport
|
J:154356
|
decreased splenocyte apoptosis
|
J:154356
|
Steap4tm1Dgen/Steap4tm1Dgen
(involves: 129P2/OlaHsd)
|
decreased adipocyte glucose uptake
|
J:187736
|
decreased muscle cell glucose uptake
|
J:187736
|
oxidative stress
|
J:187736
|
Stiltm1Mku/Stiltm1Mku
(Not Specified)
|
abnormal apoptosis
|
J:55887
|
Stim1Gt(GST050)Byg/Stim1Gt(GST050)Byg
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:178553
|
Stim1tm1.1Kuro/Stim1tm1.1Kuro
(C57BL/6-Stim1tm1.1Kuro)
|
decreased mast cell degranulation
|
J:130477
|
Stim1tm1.1Rao/Stim1tm1.1Rao
(involves: BALB/cJ * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:133262
|
Stim1tm1.1Rao/Stim1tm1.1Rao Stim2tm1.1Rao/Stim2tm1.1Rao
(involves: C57BL/6)
|
decreased cellular sensitivity to hydrogen peroxide
|
J:175075
|
Stim1tm1Kuro/Stim1tm1Kuro Cd79atm1(cre)Reth/Cd79a+
(involves: BALB/c * C57BL/6)
|
decreased B cell proliferation
|
J:172608
|
Stim1tm1Kuro/Stim1tm1Kuro Stim2tm1.1Kuro/Stim2tm1.1Kuro Cd79atm1(cre)Reth/Cd79a+
(involves: BALB/c * C57BL/6)
|
decreased B cell proliferation
|
J:172608
|
Stim1tm1Rao/Stim1tm1Rao Stim2tm1Rao/Stim2tm1Rao Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * DBA/2 * SJL)
|
decreased T cell proliferation
|
J:133262
|
Stim1tm3Ics/Stim1+
(involves: C57BL/6N)
|
abnormal oxidative phosphorylation
|
J:327797
|
decreased mitochondrial number
|
J:327797
|
increased endoplasmic reticulum stress
|
J:327797
|
increased skeletal muscle cell apoptosis
|
J:327797
|
increased skeletal muscle fiber mitochondrial size
|
J:277842
|
Stim2tm1.1Rao/Stim2tm1.1Rao
(involves: BALB/cJ * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:133262
|
Stim2tm1Beni/Stim2tm1Beni
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased neuron apoptosis
|
J:159604
|
Sting1gt/Sting1gt
(involves: C57BL/6)
|
decreased enterocyte apoptosis
|
J:269933
|
Stip1tm1.2Mamp/Stip1+
(involves: C57BL/6)
|
abnormal double-strand DNA break repair
|
J:201097
|
Stip1tm1.2Mamp/Stip1tm1.2Mamp
(involves: C57BL/6)
|
abnormal double-strand DNA break repair
|
J:201097
|
decreased fibroblast proliferation
|
J:201097
|
increased cell death
|
J:201097
|
increased embryonic tissue cell apoptosis
|
J:201097
|
Stk3tm1.1Jav/Stk3tm1.1Jav Stk4tm1Kina/Stk4tm1Kina Tg(Nkx2-1-cre)2Sand/?
(involves: 129 * C57BL/6)
|
increased lung endothelial cell proliferation
|
J:197340
|
Stk3tm1.1Jav/Stk3tm1Jav Stk4Gt(AJ0315)Wtsi/Stk4Gt(AJ0315)Wtsi
(involves: 129 * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:153945
|
increased hepatocyte proliferation
|
J:153945
|
Stk3tm1.1Rjo/Stk3tm1.1Rjo Stk4tm1.1Rjo/Stk4tm1.1Rjo Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * CD-1 * DBA * SJL)
|
increased hepatocyte apoptosis
|
J:156531
|
increased hepatocyte proliferation
|
J:156531
|
Stk3tm1.1Yy/Stk3+ Stk4tm1.1Yy/Stk4tm1.1Yy
(involves: C57BL/6 * CBA)
|
decreased hepatocyte apoptosis
|
J:156541
|
Stk3tm1.1Yy/Stk3tm1.1Yy Stk4tm1.1Yy/Stk4tm1.1Yy
(involves: C57BL/6 * CBA)
|
decreased fibroblast apoptosis
|
J:156541
|
decreased hepatocyte apoptosis
|
J:156541
|
Stk3tm1.1Yy/Stk3tm1Yy Stk4tm1.1Yy/Stk4tm1.1Yy
(involves: C57BL/6 * CBA)
|
decreased hepatocyte apoptosis
|
J:156541
|
Stk3tm1.1Yy/Stk3tm1Yy Stk4tm1.1Yy/Stk4tm1.1Yy Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * CBA * DBA)
|
increased hepatocyte apoptosis
|
J:156541
|
increased hepatocyte proliferation
|
J:156541
|
Stk3tm1.1Yy/Stk3tm1Yy Stk4tm1.1Yy/Stk4tm1.1Yy Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * CBA)
|
increased hepatocyte proliferation
|
J:156541
|
Stk3tm1Dlim/Stk3tm1Dlim Stk4tm1Dlim/Stk4tm1Dlim
(Not Specified)
|
abnormal cell proliferation
|
J:155001
|
increased embryonic tissue cell apoptosis
|
J:155001
|
increased placenta apoptosis
|
J:155001
|
Stk3tm1Jav/Stk3tm1Jav Stk4Gt(AJ0315)Wtsi/Stk4Gt(AJ0315)Wtsi
(involves: 129 * C57BL/6)
|
increased hepatocyte proliferation
|
J:153945
|
Stk4Gt(AJ0315)Wtsi/Stk4Gt(AJ0315)Wtsi
(B6.129P2-Stk4Gt(AJ0315)Wtsi)
|
increased T cell apoptosis
|
J:142674
|
increased T cell proliferation
|
J:142674
|
Stk4tm1.1Kina/Stk4tm1.1Kina
(involves: C57BL/6)
|
abnormal leukocyte adhesion
|
J:148791
|
abnormal leukocyte migration
|
J:148791
|
increased T cell proliferation
|
J:148791
|
Stk11tm1.1Arte/Stk11tm1.1Arte
(involves: C57BL/6J)
|
abnormal cell physiology
|
J:208379
|
Stk11tm1.1Rdp/Stk11tm1.1Rdp H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S6/SvEvTac * C57BL/6J * CBA/J)
|
abnormal axon extension
|
J:305107
|
Stk11tm1.1Rdp/Stk11tm1.1Rdp Tg(Pdx1-cre)89.1Dam/0
(involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N * ICR)
|
increased pancreas apoptosis
|
J:134078
|
Stk11tm1.1Sjm/Stk11tm1.1Sjm Tg(Mx1-cre)1Cgn/0
(involves: C57BL/6 * CBA * SJL)
|
abnormal mitotic spindle morphology
|
J:165090
|
aneuploidy
|
J:165090
|
cellular phenotype
|
J:165090
|
increased mitochondrial fission
|
J:165090
|
Stk11tm1.2Rdp/Stk11tm1.2Rdp
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL)
|
abnormal cell cycle
|
J:78818
|
abnormal cell physiology
|
J:78818
|
Stk11tm1.2Rdp/Stk11tm1.2Rdp
(involves: 129S6/SvEvTac)
|
abnormal cell differentiation
|
J:141132
|
Stk11tm1Keis/Stk11tm1Keis Tg(Ckmm-cre)5Khn/0
(involves: FVB)
|
decreased muscle cell glucose uptake
|
J:98513
|
Stk17btm1Hed/Stk17btm1Hed
(involves: 129X1/SvJ * C57BL/6)
|
increased T cell proliferation
|
J:94685
|
Stk17btm1Hed/Stk17btm1Hed
(B6.129X1-Stk17btm1Hed)
|
increased T cell proliferation
|
J:94685
|
Stk25tm1.1Bwh/Stk25tm1.1Bwh
(involves: 129 * C57BL/6)
|
abnormal neuronal migration
|
J:203414
|
Stk26tm2.1Zzh/Stk26tm2.1Zzh
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal enterocyte proliferation
|
J:322311
|
abnormal intestinal goblet cell morphology
|
J:322311
|
Stk33tm1.2Csll/Stk33tm1.2Csll
(B6.Cg-Stk33tm1.2Csll)
|
abnormal sperm flagellum morphology
|
J:253666
|
asthenozoospermia
|
J:253666
|
Stk35tm1Kll/Stk35tm1Kll
(B6.Cg-Stk35tm1Kll)
|
decreased male germ cell number
|
J:264258
|
Stk36tm1Ptch/Stk36tm1Ptch Tg(Ddx4-cre)1Ptch/0
(involves: 129P2/OlaHsd)
|
abnormal manchette morphology
|
J:208762
|
abnormal sperm axoneme morphology
|
J:208762
|
abnormal sperm fibrous sheath morphology
|
J:208762
|
abnormal sperm flagellum morphology
|
J:208762
|
abnormal sperm head morphology
|
J:208762
|
abnormal sperm nucleus morphology
|
J:208762
|
abnormal sperm principal piece morphology
|
J:208762
|
abnormal spermatid morphology
|
J:208762
|
absent sperm head
|
J:208762
|
decreased activated sperm motility
|
J:208762
|
decreased sperm progressive motility
|
J:208762
|
elongated manchette
|
J:208762
|
oligozoospermia
|
J:208762
|
Stk38em1Flca/Stk38em1Flca
(C57BL/6-Stk38em1Flca)
|
increased retina apoptosis
|
J:265036
|
Stk38em2Flca/Stk38em2Flca
(C57BL/6-Stk38em2Flca)
|
increased retina apoptosis
|
J:265036
|
Stk38tm1Hem/Stk38+
(involves: 129P2/Ola * C57BL/6)
|
decreased sensitivity to induced cell death
|
J:185408
|
Stk38tm1Hem/Stk38tm1Hem
(involves: 129P2/Ola * C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:185408
|
decreased sensitivity to induced cell death
|
J:185408
|
decreased thymocyte apoptosis
|
J:185408
|
Stk38ltm1b(KOMP)Wtsi/Stk38ltm1b(KOMP)Wtsi
(B6J.B6N(FVB)-Stk38ltm1b(KOMP)Wtsi)
|
increased retina apoptosis
|
J:265036
|
Stk40tm1Nju/Stk40tm1Nju
(B6.129-Stk40tm1Nju)
|
increased lung apoptosis
|
J:196001
|
Stmn2em1Jmi/Stmn2em1Jmi
(C57BL/6N-Stmn2em1Jmi)
|
abnormal microtubule cytoskeleton morphology
|
J:337175
|
abnormal mitochondrial shape
|
J:337175
|
delayed axon extension
|
J:337175
|
Stmp1em1Eno/Stmp1em1Eno
(C57BL/6-Stmp1em1Eno)
|
abnormal respiratory electron transport chain
|
J:325962
|
Ston1tm1.1Tmar/Ston1tm1.1Tmar
(involves: C57BL/6J)
|
abnormal cell adhesion
|
J:227201
|
abnormal cell morphology
|
J:227201
|
abnormal fibroblast migration
|
J:227201
|
abnormal vesicle-mediated transport
|
J:227201
|
Stpg4em1Ogu/Stpg4em1Ogu
(involves: C57BL/6 * DBA/2)
|
abnormal DNA methylation
|
J:254851
|
Stra6tm1Nbg/Stra6tm1Nbg
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal adipocyte glucose uptake
|
J:203449
|
Stra8em4Keish/Stra8em4Keish
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal male meiosis
|
J:290712
|
arrest of male meiosis
|
J:290712
|
azoospermia
|
J:290712
|
Stra8tm1.1Nbg/Stra8tm1.1Nbg
(involves: 129S2/SvPas * C57BL/6)
|
abnormal male meiosis
|
J:139646
|
absent oocytes
|
J:139646
|
arrest of male meiosis
|
J:139646
|
azoospermia
|
J:139646
|
Stra8tm1Dcp/Stra8tm1Dcp
(involves: 129S4/SvJae * C57BL/6)
|
abnormal female meiosis
|
J:107319
|
Stra8tm1Ysa/Stra8tm1Ysa
(involves: C57BL/6NCrlj * CBA/JNCrlj * Jcl:MCH(ICR))
|
abnormal female meiosis
|
J:205334
|
Stradaem1Pbcr/Stradaem1Pbcr
(C57BL/6N-Stradaem1Pbcr)
|
abnormal neuronal migration
|
J:308972
|
StrbpGt(pGT1.8geo)8Pgr/StrbpGt(pGT1.8geo)8Pgr
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
asthenozoospermia
|
J:69466
|
oligozoospermia
|
J:69466
|
Strip1tm1b(KOMP)Wtsi/Strip1tm1b(KOMP)Wtsi
(involves: C57BL/6 * C57BL/6N * FVB/NJ)
|
decreased fibroblast cell migration
|
J:251816
|
stu/stu
(involves: C3H/HeJ)
|
abnormal Purkinje cell differentiation
|
J:6464
|
stu/stu
(involves: C3H/HeJ * C57BL/6J)
|
abnormal Purkinje cell mitochondrial morphology
|
J:28094
|
Stub1tm1Cpat/Stub1tm1Cpat
(involves: 129S/SvEv * C57BL/6)
|
abnormal apoptosis
|
J:86213
|
abnormal cell physiology
|
J:86213
|
increased thymocyte apoptosis
|
J:86213
|
Stx2repro34/Stx2repro34
(involves: C3HeB/FeJ * C57BL/6J)
|
arrest of male meiosis
|
J:92463,
J:136575
|
azoospermia
|
J:92463,
J:136575
|
multinucleated giant male germ cells
|
J:136575
|
Stx2tm1Dcru/Stx2+
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal small intestinal crypt cell proliferation
|
J:110376
|
Stx2tm1Dcru/Stx2tm1Dcru
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal small intestinal crypt cell proliferation
|
J:110376
|
azoospermia
|
J:110376
|
increased male germ cell apoptosis
|
J:110376
|
Stx3Gt(EUCE320f12)1.1Hmgu/Stx3Gt(EUCE320f12)1.1Hmgu Tg(Cma1-cre)ARoer/0
(B6.Cg-Stx3Gt(EUCE320f12)1.1Hmgu Tg(Cma1-cre)ARoer)
|
abnormal mast cell degranulation
|
J:275367
|
decreased mast cell degranulation
|
J:275367
|
Stx3Gt(EUCE320f12)1.2Hmgu/Stx3+
(B6.129P2(Cg)-Stx3Gt(EUCE320f12)1.2Hmgu)
|
abnormal mast cell degranulation
|
J:275367
|
Stx11tm1.2Ics/Stx11tm1.2Ics
(involves: C57BL/6NTac)
|
decreased NK cell degranulation
|
J:193137
|
Stxbp2m1Anu/Stxbp2m1Anu
(C57BL/6NCrlAnu-Stxbp2m1Anu)
|
abnormal cell morphology
|
J:104190
|
Stxbp2tm1Bdic/Stxbp2+
(involves: 129S * C57BL/6)
|
decreased mast cell degranulation
|
J:188931
|
Styxtm1.1Jedi/Styxtm1.1Jedi
(either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6))
|
abnormal germ cell morphology
|
J:74767
|
asthenozoospermia
|
J:74767
|
Styxtm1Jedi/Styxtm1Jedi
(either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) or (involves: C57BL/6))
|
asthenozoospermia
|
J:74767
|
decreased spermatid number
|
J:74767
|
globozoospermia
|
J:74767
|
teratozoospermia
|
J:74767
|
Styxl1em1Xjg/Styxl1em1Xjg
(involves: C57BL/6J)
|
abnormal acrosome morphology
|
J:351148
|
abnormal manchette morphology
|
J:351148
|
abnormal outer dense fiber morphology
|
J:351148
|
abnormal sperm axoneme morphology
|
J:351148
|
abnormal sperm end piece morphology
|
J:351148
|
abnormal sperm flagellum morphology
|
J:351148
|
abnormal sperm head morphology
|
J:351148
|
abnormal sperm nucleus morphology
|
J:351148
|
abnormal spermatid morphology
|
J:351148
|
absent sperm axonemal central pair
|
J:351148
|
asthenozoospermia
|
J:351148
|
coiled sperm flagellum
|
J:351148
|
decreased sperm progressive motility
|
J:351148
|
elongated manchette
|
J:351148
|
oligozoospermia
|
J:351148
|
teratozoospermia
|
J:351148
|
Styxl1em2Xjg/Styxl1em2Xjg
(involves: C57BL/6J)
|
abnormal sperm head morphology
|
J:351148
|
abnormal sperm nucleus morphology
|
J:351148
|
asthenozoospermia
|
J:351148
|
coiled sperm flagellum
|
J:351148
|
decreased sperm progressive motility
|
J:351148
|
oligozoospermia
|
J:351148
|
teratozoospermia
|
J:351148
|
Sucla2Gt(IST10208H1)Tigm/Sucla2+
(involves: 129S/SvEv * C57BL/6N)
|
abnormal mitochondrial physiology
|
J:241325
|
abnormal oxidative phosphorylation
|
J:241325
|
cellular phenotype
|
J:241325
|
decreased hepatocyte mitochondrial DNA content
|
J:241325
|
decreased mitochondrial DNA content
|
J:241325
|
decreased myocardial fiber mitochondrial DNA content
|
J:241325
|
Sucla2Gt(IST10208H1)Tigm/Sucla2+ Suclg2Gt(Ayu21-KBW131)Imeg/Suclg2+
(involves: 129S/SvEv * C57BL/6 * C57BL/6N)
|
abnormal oxidative phosphorylation
|
J:241325
|
decreased hepatocyte mitochondrial DNA content
|
J:241325
|
decreased mitochondrial DNA content
|
J:241325
|
Sucla2Gt(SAbetageo)1Bhg/Sucla2+
(involves: 129S6/SvEvTac * C57BL/6)
|
increased mitochondrial DNA content
|
J:213453
|
Sucla2Gt(SAbetageo)1Bhg/Sucla2Gt(SAbetageo)1Bhg
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal mitochondrial morphology
|
J:213453
|
abnormal mitochondrial physiology
|
J:213453
|
decreased mitochondrial DNA content
|
J:213453
|
increased mitochondrial DNA content
|
J:213453
|
Suclg2Gt(Ayu21-KBW131)Imeg/Suclg2+
(involves: C57BL/6 * C57BL/6N)
|
abnormal mitochondrial physiology
|
J:241325
|
Sucnr1tm1Dgen/Sucnr1tm1Dgen
(B6.129P2-Sucnr1tm1Dgen)
|
decreased T cell proliferation
|
J:143337
|
SucoGt(KST050)Byg/SucoGt(KST050)Byg
(involves: 129P2/OlaHsd * C57BL/6 * CD-1)
|
abnormal osteoblast physiology
|
J:159823
|
impaired osteoblast differentiation
|
J:159823
|
increased osteoblast apoptosis
|
J:159823
|
Suds3tm1.1Rdp/Suds3+ Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6 * FVB)
|
aneuploidy
|
J:117829
|
Suds3tm1Rdp/Suds3tm1Rdp
(involves: 129S6/SvEvTac)
|
abnormal cell cycle
|
J:86008
|
abnormal chromosome morphology
|
J:86008
|
aneuploidy
|
J:86008
|
polyploidy
|
J:86008
|
Sugt1Gt(RRS405)Byg/Sugt1+ Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129P2/OlaHsd * C57BL/6J)
|
cellular phenotype
|
J:226313
|
Sulf1tm1Clrm/Sulf1tm1Clrm
(involves: 129S2/SvPas * C57BL/6)
|
increased fibroblast proliferation
|
J:116527
|
Sulf1tm1Clrm/Sulf1tm1Clrm Sulf2tm1Clrm/Sulf2tm1Clrm
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell physiology
|
J:116527
|
Sulf1tm1Mmas/Sulf1tm1Mmas
(B6N.129P2-Sulf1tm1Mmas)
|
abnormal cell morphology
|
J:183277
|
Sulf1tm1Mmas/Sulf1tm1Mmas Sulf2tm1Mmas/Sulf2tm1Mmas
(B6N.129P2-Sulf1tm1Mmas Sulf2tm1Mmas)
|
abnormal cell morphology
|
J:183277
|
Sulf2tm1Clrm/Sulf2tm1Clrm
(involves: 129S2/SvPas * C57BL/6)
|
increased fibroblast proliferation
|
J:116527
|
Sulf2tm1Mmas/Sulf2tm1Mmas
(B6N.129P2-Sulf2tm1Mmas)
|
abnormal cell morphology
|
J:183277
|
Sult1a1tm1Glatt/Sult1a1tm1Glatt
(FVB.Cg-Sult1a1tm1Glatt)
|
abnormal cell physiology
|
J:217578
|
Sult1d1tm1Glatt/Sult1d1tm1Glatt
(FVB.Cg-Sult1d1tm1Glatt)
|
abnormal cell physiology
|
J:217578
|
Sult1e1tm1Song/Sult1e1tm1Song
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal sperm motility
|
J:96133
|
Sumf1Gt(RST760)Byg/Sumf1Gt(RST760)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased hepatocyte apoptosis
|
J:120146
|
increased neuron apoptosis
|
J:120146
|
Sumo1Gt(XA024)Byg/Sumo1Gt(XA024)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal PML bodies
|
J:141678
|
Sumo2tm1Weiy/Sumo2tm1Weiy
(involves: 129 * C57BL/6)
|
decreased cell proliferation
|
J:217019
|
increased apoptosis
|
J:217019
|
Sun1em1Leim/Sun1em1Leim
(C57BL/6-Sun1em1Leim)
|
abnormal meiotic attachment of telomere to nuclear envelope
|
J:270644
|
Sun1tm1.1Ktj/Sun1tm1.1Ktj
(involves: C57BL/6J * FVB/N)
|
abnormal male meiosis
|
J:146636
|
absent oocytes
|
J:146636
|
arrest of male meiosis
|
J:146636
|
azoospermia
|
J:146636
|
Sun1tm1.1Ktj/Sun1tm1.1Ktj
(Not Specified)
|
abnormal male meiosis
|
J:194067
|
Sun1tm1.1Ktj/Sun1tm1.1Ktj
(involves: 129/Sv * C57BL/6 * C57BL/6N)
|
abnormal Purkinje cell migration
|
J:224769
|
Sun1tm1.1Ktj/Sun1tm1.1Ktj Sun2tm1.1Cyh/Sun2+
(involves: 129/Sv * C57BL/6 * C57BL/6N)
|
abnormal Purkinje cell migration
|
J:224769
|
Sun1tm1Mhan/Sun1tm1Mhan
(involves: 129S6/SvEvTac)
|
abnormal chromosomal synapsis
|
J:122602
|
abnormal female meiosis
|
J:122602
|
abnormal spermatocyte morphology
|
J:122602
|
absent oocytes
|
J:122602
|
arrest of male meiosis
|
J:122602
|
decreased male germ cell number
|
J:122602
|
increased ovary apoptosis
|
J:122602
|
increased testis apoptosis
|
J:122602
|
Sun1tm1Mhan/Sun1tm1Mhan
(B6.129S6-Sun1tm1Mhan)
|
abnormal male meiosis
|
J:205574
|
abnormal meiotic attachment of telomere to nuclear envelope
|
J:205574
|
Sun1tm1Mhan/Sun1tm1Mhan
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal chromosomal synapsis
|
J:209347
|
abnormal male meiosis
|
J:209347
|
Sun3em1Qsh/Sun3em1Qsh
(Not Specified)
|
abnormal manchette morphology
|
J:298937
|
abnormal sperm midpiece morphology
|
J:298937
|
globozoospermia
|
J:298937
|
increased male germ cell apoptosis
|
J:298937
|
oligozoospermia
|
J:298937
|
Sun5em1Wli/Sun5em1Wli
(involves: C57BL/6J * DBA/2)
|
abnormal sperm axoneme morphology
|
J:247612
|
abnormal sperm connecting piece morphology
|
J:247612
|
abnormal sperm head morphology
|
J:247612
|
absent sperm head
|
J:247612
|
globozoospermia
|
J:247612
|
teratozoospermia
|
J:247612
|
Supv3l1tm1Whle/Supv3l1+
(involves: 129P2/OlaHsd * C57BL/6)
|
maternal effect
|
J:193361
|
Supv3l1tm2.1Jkl/Supv3l1tm2.2Jkl Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * FVB/N)
|
increased macrophage derived foam cell number
|
J:144991
|
Supv3l1tm2Jkl/Supv3l1tm2Jkl Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129P2/OlaHsd * C57BL/6)
|
increased macrophage derived foam cell number
|
J:144991
|
Supv3l1tm2Jkl/Supv3l1tm2Jkl Tg(Mx1-cre)1Cgn/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
increased macrophage derived foam cell number
|
J:144991
|
Surf1tm1Zev/Surf1tm1Zev
(involves: 129S7/SvEvBrd * C57BL/6J * DBA/2)
|
abnormal respiratory electron transport chain
|
J:81773
|
Surf1tm1Zev/Surf1tm1Zev Tg(Ckm-Ppargc1a)31Brsp/0
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal aerobic respiration
|
J:176080
|
increased mitochondrial fission
|
J:176080
|
Surf1tm2.1Zev/Surf1tm2.1Zev
(involves: 129S7/SvEvBrd * C57BL/6 * DBA/2)
|
abnormal mitochondrial physiology
|
J:117871
|
decreased susceptibility to neuronal excitotoxicity
|
J:117871
|
Suv39h1tm1Jnw/Suv39h1tm1Jnw Suv39h2tm1Jnw/Suv39h2tm1Jnw
(involves: 129 * C57BL/6J)
|
arrest of male meiosis
|
J:72503
|
Suz12Gt(Betageo)1Khe/Suz12Gt(Betageo)1Khe
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cell proliferation
|
J:93307
|
increased embryonic tissue cell apoptosis
|
J:93307
|
Sv2atm1Baj/Sv2atm1Baj
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:70828
|
Sv2atm1Baj/Sv2atm1Baj Sv2btm1Baj/Sv2btm1Baj
(involves: 129 * C57BL/6)
|
abnormal cell physiology
|
J:70828
|
Swap70tm1Jess/Swap70tm1Jess
(involves: 129T2/SvEms * 129X1/SvJ)
|
increased cellular sensitivity to gamma-irradiation
|
J:71160
|
swm2/swm2
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal sperm midpiece morphology
|
J:117563
|
abnormal sperm mitochondrial sheath morphology
|
J:117563
|
abnormal sperm nucleus morphology
|
J:117563
|
abnormal sperm principal piece morphology
|
J:117563
|
abnormal spermatid morphology
|
J:117563
|
absent sperm flagellum
|
J:86161
|
absent sperm head
|
J:117563
|
immotile sperm
|
J:117563
|
oligozoospermia
|
J:117563,
J:86161
|
short sperm flagellum
|
J:117563
|
teratozoospermia
|
J:117563
|
swm6/swm6
(involves: C3HeB/FeJ * C57BL/6)
|
azoospermia
|
J:86161
|
Swsap1em1Mjn/Swsap1em1Mjn
(involves: C57BL/6J * CBA/J)
|
abnormal chromosomal synapsis
|
J:268570
|
abnormal chromosome morphology
|
J:268570
|
arrest of male meiosis
|
J:268570
|
azoospermia
|
J:268570
|
increased male germ cell apoptosis
|
J:268570
|
increased ovary apoptosis
|
J:268570
|
Syce1em1Rrca/Syce1em1Rrca
(involves: C57BL/6J)
|
abnormal chromosomal synapsis
|
J:309952
|
absent oocytes
|
J:309952
|
arrest of male meiosis
|
J:309952
|
azoospermia
|
J:309952
|
Syce1tm1Hgu/Syce1tm1Hgu
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:146770
|
abnormal synaptonemal complex
|
J:146770
|
arrest of male meiosis
|
J:146770
|
azoospermia
|
J:146770
|
increased male germ cell apoptosis
|
J:146770
|
Syce2Gt(FHCRC-GT-S8-7E1)Sor/Syce2Gt(FHCRC-GT-S8-7E1)Sor
(involves: C57BL/6)
|
abnormal female meiosis
|
J:119809
|
abnormal male meiosis
|
J:119809
|
arrest of male meiosis
|
J:119809
|
Syce3tm1Rben/Syce3tm1Rben
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal chromosomal synapsis
|
J:172714
|
abnormal female meiosis
|
J:172714
|
abnormal male meiosis
|
J:172714
|
abnormal meiosis
|
J:172714
|
abnormal synaptonemal complex
|
J:172714
|
azoospermia
|
J:172714
|
Sycp1tm1Aps/Sycp1tm1Aps
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal male meiosis
|
J:98718
|
arrest of male meiosis
|
J:98718
|
azoospermia
|
J:98718
|
Sycp1tm1Aps/Sycp1tm1Aps
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal male meiosis
|
J:187173
|
Sycp2tm1Jw/Sycp2tm1Jw
(involves: 129S4/SvJae * C57BL/6)
|
abnormal female meiosis
|
J:111287
|
arrest of male meiosis
|
J:111287
|
azoospermia
|
J:111287
|
increased male germ cell apoptosis
|
J:111287
|
Sycp2ltm1Jw/Sycp2ltm1Jw
(involves: 129S4/SvJae * C57BL/6)
|
decreased oocyte number
|
J:225272
|
Sycp3tm1Hoog/Sycp3tm1Hoog
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal spermatocyte morphology
|
J:60153
|
arrest of male meiosis
|
J:60153
|
azoospermia
|
J:60153
|
Sycp3tm1Hoog/Sycp3tm1Hoog
(involves: 129P2/OlaHsd * C57BL/6NCrl)
|
abnormal female meiosis
|
J:76511
|
Syde1tm1.1Hwch/Syde1tm1.1Hwch
(involves: C57BL/6J)
|
increased apoptosis
|
J:241798
|
Syf2Gt(PST25562)Mfgc/Syf2Gt(PST25562)Mfgc
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:187030
|
Syislem1Bzuo/Syislem1Bzuo
(involves: C57BL/6)
|
abnormal myoblast differentiation
|
J:266240
|
abnormal myoblast fusion
|
J:266240
|
decreased myoblast proliferation
|
J:266240
|
Syktm1.1Tara/Syktm1.1Tara
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:114816
|
Syktm1Tyb/Syktm1Tyb
(involves: 129S2/SvPas * C57BL/6)
|
abnormal osteoclast differentiation
|
J:89583
|
Syktm1Tyb/Syktm1Tyb
(involves: 129S2/SvPas)
|
impaired neutrophil phagocytosis
|
J:155479
|
Syktm2.1(ZAP70)Fkfr/Syktm2.1(ZAP70)Fkfr
(B6.129-Syktm2.1(ZAP70)Fkfr)
|
increased B cell apoptosis
|
J:188422
|
increased mesangial cell number
|
J:188422
|
Syn3tm1Pggd/Syn3tm1Pggd
(involves: 129X1/SvJ)
|
delayed axon extension
|
J:77048
|
Syne1tm1Chen/Syne1tm1Chen Syne2tm1.1Chen/Syne2tm1.1Chen
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss)
|
abnormal cell nucleus morphology
|
J:211007
|
Syne1tm1Chen/Syne1tm1Chen Syne2tm1.1Chen/Syne2tm1.1Chen Tg(Nkx2-5-cre)9Eno/?
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss)
|
abnormal cell nucleus morphology
|
J:211007
|
increased cardiomyocyte apoptosis
|
J:211007
|
Syne1tm1Chen/Syne1tm1Chen Tg(Nkx2-5-cre)9Eno/?
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss)
|
abnormal cell nucleus morphology
|
J:211007
|
Syne2cpfl8/Syne2cpfl8
(B6.Cg-Syne2cpfl8/Boc)
|
abnormal cell nucleus morphology
|
J:229433
|
increased retina apoptosis
|
J:229433
|
Syne2tm1Ngl/Syne2tm1Ngl
(involves: 129 * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:139778
|
decreased fibroblast cell migration
|
J:139778
|
Syngap1tm1.1Mabk/Syngap1tm1.1Mabk
(involves: 129S1/Sv * C57BL/6)
|
increased neuron apoptosis
|
J:101084
|
Syngap1tm1.1Mabk/Syngap1tm1.2Mabk Tg(Camk2a-cre)2834Lusc/0
(involves: 129S1/Sv * C57BL/6)
|
increased neuron apoptosis
|
J:101084
|
Sypl1tm1b(KOMP)Wtsi/Sypl1tm1b(KOMP)Wtsi
(C57BL/6N-Sypltm1b(KOMP)Wtsi)
|
abnormal intracellular organelle morphology
|
J:339267
|
abnormal sperm connecting piece morphology
|
J:339267
|
abnormal sperm head morphology
|
J:339267
|
abnormal sperm midpiece morphology
|
J:339267
|
asthenozoospermia
|
J:339267
|
decreased sperm progressive motility
|
J:339267
|
kinked sperm flagellum
|
J:339267
|
teratozoospermia
|
J:339267
|
Syt7tm1Nan/Syt7tm1Nan
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell physiology
|
J:85201
|
Syvn1tm1Tn/Syvn1+
(D1.Cg-Syvn1tm1Tn)
|
increased apoptosis
|
J:86009
|
Syvn1tm1Tn/Syvn1tm1Tn
(D1.Cg-Syvn1tm1Tn)
|
abnormal apoptosis
|
J:86009
|
T(7;18)50H/+
(involves: 101/H * C3H/HeH * C57BL/6J)
|
abnormal sperm head morphology
|
J:23104
|
multivalent meiotic configurations
|
J:23104
|
oligozoospermia
|
J:23104
|
T(7;18)50H/+
(involves: 101/H * C3H/HeH)
|
maternal imprinting
|
J:3618
|
paternal imprinting
|
J:3618
|
uniparental disomy
|
J:3618
|
T(7;18)50H/+
(involves: 101/H * C3H/HeH * CBA/H)
|
abnormal sperm head morphology
|
J:23104
|
multivalent meiotic configurations
|
J:23104
|
oligozoospermia
|
J:23104
|
T(7;18)50H/T(7;18)50H
(involves: 101/H * C3H/HeH)
|
multivalent meiotic configurations
|
J:23104
|
T(7;18)50H/+
(involves: 101/H * C3H/HeH * CBA/H)
|
abnormal sperm head morphology
|
J:23104
|
multivalent meiotic configurations
|
J:23104
|
oligozoospermia
|
J:23104
|
T(7;18)50H/+
(involves: 101/H * C3H/HeH * C57BL/6J)
|
abnormal sperm head morphology
|
J:23104
|
multivalent meiotic configurations
|
J:23104
|
oligozoospermia
|
J:23104
|
T(7;18)50H/+
(involves: 101/H * C3H/HeH)
|
maternal imprinting
|
J:3618
|
paternal imprinting
|
J:3618
|
uniparental disomy
|
J:3618
|
T(7;18)50H/T(7;18)50H
(involves: 101/H * C3H/HeH)
|
multivalent meiotic configurations
|
J:23104
|
T(7;19)145H/?
(involves: 101/H * C3H/HeH)
|
arrest of male meiosis
|
J:34742
|
azoospermia
|
J:34742
|
T(7;19)145H/?
(involves: 101/H * C3H/HeH)
|
arrest of male meiosis
|
J:34742
|
azoospermia
|
J:34742
|
t6/Tagaptm1Bgh
(involves: BALB/c * BTBR/TF * FVB/N)
|
abnormal male meiosis
|
J:100859
|
abnormal meiosis
|
J:100859
|
abnormal sperm motility
|
J:100859
|
asthenozoospermia
|
J:100859
|
tw2/tw2
(Not Specified)
|
abnormal manchette morphology
|
J:89468
|
teratozoospermia
|
J:89468
|
tw8/tw8
(Not Specified)
|
abnormal manchette assembly
|
J:89468
|
abnormal sperm head morphology
|
J:89468
|
abnormal sperm nucleus morphology
|
J:89468
|
teratozoospermia
|
J:89468
|
tw73/tw73
(involves: M. m. musculus)
|
decreased embryonic epiblast cell proliferation
|
J:175675
|
Tab1tm1Geny/Tab1tm1Geny
(involves: C57BL/6 * CBA)
|
abnormal cell physiology
|
J:80766
|
Tab2tm2.1Aki/Tab2tm2.1Aki Tab3tm1Aki/Tab3tm1Aki Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:195289
|
increased B cell apoptosis
|
J:195289
|
Tabl/Y
(STOCK Tabl/GrsrJ)
|
azoospermia
|
J:233070
|
Tacc3tm1.1Tno/Tacc3tm1.2Tno
(involves: C57BL/6)
|
abnormal mitosis
|
J:126471
|
Tacc3tm1Tno/Tacc3tm1Tno
(involves: C57BL/6)
|
abnormal mitosis
|
J:126471
|
Taco1m1Anu/Taco1m1Anu
(C57BL/6-Taco1m1Anu)
|
abnormal respiratory electron transport chain
|
J:239883
|
Tada3tm1.1Viba/Tada3tm1.1Viba
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal mitosis
|
J:190249
|
decreased fibroblast proliferation
|
J:190249
|
Tada3tm1.2Viba/Tada3tm1.2Viba
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N * SJL)
|
abnormal trophoblast giant cell proliferation
|
J:190249
|
Taf1btm1c(EUCOMM)Hmgu/Taf1btm1c(EUCOMM)Hmgu Trp53tm1Tyj/Trp53tm1Tyj Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sortm1(cre/ERT)Nat
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * C57BL/6N)
|
abnormal nucleolus morphology
|
J:321558
|
Taf4tm1.1Idvd/Taf4tm1.1Idvd
(Not Specified)
|
decreased fibroblast apoptosis
|
J:125257
|
increased fibroblast proliferation
|
J:125257
|
Taf4tm1Idvd/Taf4tm1Idvd Tg(KRT14-cre/ERT2)1Ipc/0
(involves: C57BL/6 * SJL)
|
increased keratinocyte proliferation
|
J:124111
|
Taf4btm1Rtj/Taf4btm1Rtj
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal oocyte morphology
|
J:156655,
J:71679
|
decreased granulosa cell proliferation
|
J:119191
|
decreased oocyte number
|
J:156655
|
increased granulosa cell apoptosis
|
J:119191
|
Taf4btm1Rtj/Taf4btm1Rtj
(B6.129-Taf4btm1Rtj)
|
abnormal acrosome assembly
|
J:97245
|
abnormal spermatogonia proliferation
|
J:97245
|
asthenozoospermia
|
J:97245
|
decreased male germ cell number
|
J:97245
|
oligozoospermia
|
J:97245
|
Taf7tm1.1Dss/Taf7tm1.2Dss Tg(Cd8a*-cre)B8Asin/0
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:185745
|
Taf7ltm1.1Jw/Y
(B6J.Cg-Taf7ltm1.1Jw)
|
abnormal brown fat cell differentiation
|
J:228546
|
abnormal mitochondrial physiology
|
J:228546
|
asthenozoospermia
|
J:121371
|
hairpin sperm flagellum
|
J:121371
|
kinked sperm flagellum
|
J:121371
|
oligozoospermia
|
J:121371
|
teratozoospermia
|
J:121371
|
Taf7ltm1.1Jw/Y
(129X1.Cg-Taf7ltm1.1Jw)
|
asthenozoospermia
|
J:121371
|
hairpin sperm flagellum
|
J:121371
|
kinked sperm flagellum
|
J:121371
|
oligozoospermia
|
J:121371
|
teratozoospermia
|
J:121371
|
Taf10tm1.1Lzt/Taf10tm1.1Lzt
(involves: 129 * C57BL/6 * SJL)
|
abnormal inner cell mass apoptosis
|
J:101819
|
absent inner cell mass proliferation
|
J:101819
|
Taf10tm1Lzt/Taf10tm1Lzt Tg(KRT14-cre)1Ipc/0
(involves: 129 * C57BL/6 * SJL)
|
abnormal keratinocyte differentiation
|
J:101668
|
Tafa2tm1Zgwg/Tafa2tm1Zgwg
(involves: C57BL/6)
|
increased brain apoptosis
|
J:271697
|
increased cellular glucose import
|
J:271697
|
Tafazzinem1Xfa/Y Tg(myl7.L-cre)1118Tmhn/0
(involves: C57BL/6NCrl * MF1)
|
abnormal cellular respiration
|
J:339058
|
abnormal mitochondrial physiology
|
J:339058
|
abnormal mitochondrial shape
|
J:339058
|
abnormal respiratory electron transport chain
|
J:339058
|
decreased mitochondrial size
|
J:339058
|
disorganized mitochondrial cristae
|
J:339058
|
increased mitochondrial number
|
J:339058
|
Tafazzintm1Dost/Y
(involves: 129P2/OlaHsd)
|
abnormal male meiosis
|
J:238324
|
abnormal spermatocyte morphology
|
J:238324
|
azoospermia
|
J:238324
|
Tal1tm2Wehi/Tal1tm2Wehi
(involves: 129S1/Sv * C57BL/6)
|
increased neuron apoptosis
|
J:58825
|
Taldo1tm1Perl/Taldo1tm1Perl
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal sperm mitochondrial morphology
|
J:114691
|
asthenozoospermia
|
J:114691
|
Tamalintm1.1Tes/Tamalintm1.1Tes
(B6.129S1-Tamalintm1.1Tes)
|
abnormal neuron differentiation
|
J:181614
|
abnormal neuron proliferation
|
J:181614
|
Tanktm1Aki/Tanktm1Aki
(involves: 129/Sv * C57BL/6)
|
increased B cell proliferation
|
J:151757
|
Tarbp2tm1Reb/Tarbp2tm1Reb
(Not Specified)
|
oligozoospermia
|
J:55515
|
Tardbptm1.1Ckjs/Tardbptm1.1Ckjs
(involves: C57BL/6J * FVB/N)
|
absent inner cell mass proliferation
|
J:155958
|
Tardbptm1.1Hiok/Tardbp+
(involves: C57BL/6J)
|
abnormal cell cycle checkpoint function
|
J:308471
|
abnormal endoplasmic reticulum morphology
|
J:308471
|
Tardbptm1.1Pcw/Tardbptm1.1Pcw Tg(CAG-cre/Esr1*)5Amc/0
(involves: 129 * C57BL/6 * CBA * SJL)
|
abnormal lipid oxidation
|
J:164406
|
Tardbptm1.1Pcw/Tardbptm1.1Pcw Tg(Stra8-icre)1Reb/0
(involves: C57BL/6 * FVB/NJ * SJL)
|
abnormal chromosomal synapsis
|
J:324061
|
abnormal chromosome morphology
|
J:324061
|
abnormal chromosome number
|
J:324061
|
abnormal double-strand DNA break repair
|
J:324061
|
abnormal sperm flagellum morphology
|
J:324061
|
abnormal sperm head morphology
|
J:324061
|
absent sperm head
|
J:324061
|
arrest of male meiosis
|
J:324061
|
decreased male germ cell number
|
J:324061
|
increased male germ cell apoptosis
|
J:324061
|
oligozoospermia
|
J:324061
|
teratozoospermia
|
J:324061
|
Tardbptm1.1Sobue/Tardbptm1.1Sobue Tg(SLC18A3-cre)Misa/0
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * C57BL/6NTac)
|
abnormal autophagosome formation
|
J:324570
|
Tarm1tm1Yiw/Tarm1tm1Yiw
(involves: C57BL/6 * C57BL/6NSlc)
|
abnormal dendritic cell differentiation
|
J:301164
|
decreased T cell proliferation
|
J:301164
|
Tas1r1tm1Uboe/Tas1r1tm1Uboe
(involves: C57BL/6)
|
increased male germ cell apoptosis
|
J:185286
|
multinucleated giant male germ cells
|
J:185286
|
Tasp1tm1.1Jjdh/Tasp1tm1.1Jjdh
(involves: 129X1/SvJ)
|
decreased cell proliferation
|
J:112159
|
Tasp1tm1.1Jjdh/Tasp1tm1.1Jjdh
(involves: 129X1/SvJ * C57BL/6)
|
azoospermia
|
J:205038
|
decreased elongated spermatid number
|
J:205038
|
decreased spermatid number
|
J:205038
|
increased male germ cell apoptosis
|
J:205038
|
Tax1bp1GT(RRJ464)Byg/Tax1bp1GT(RRJ464)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:124968
|
Tax1bp1tm1Ktj/Tax1bp1tm1Ktj
(B6.129P2-Tax1bp1tm1Ktj)
|
abnormal macrophage chemotaxis
|
J:131849
|
Tbc1d1Gt(E140H06)Wrst/Tbc1d1Gt(E140H06)Wrst
(B6.129P2-Tbc1d1Gt(E140H06)Wrst)
|
abnormal lipid oxidation
|
J:203285
|
abnormal muscle cell glucose uptake
|
J:203285
|
increased fatty acid oxidation
|
J:203285
|
Tbc1d4tm1.1Arte/Tbc1d4tm1.1Arte
(involves: C57BL/6)
|
decreased muscle cell glucose uptake
|
J:169477
|
increased adipocyte glucose uptake
|
J:169477
|
increased muscle cell glucose uptake
|
J:169477
|
Tbc1d4tm1.2Arte/Tbc1d4tm1.2Arte
(involves: C57BL/6 * CBA)
|
decreased adipocyte glucose uptake
|
J:194026
|
decreased skeletal muscle cell glucose uptake
|
J:194026
|
increased adipocyte glucose uptake
|
J:194026
|
Tbc1d4tm1Lex/Tbc1d4tm1Lex
(involves: 129S/SvEvBrd * C57BL/6J * C57BL/6N)
|
decreased adipocyte glucose uptake
|
J:191749
|
decreased skeletal muscle cell glucose uptake
|
J:191749
|
increased adipocyte glucose uptake
|
J:191749
|
Tbc1d10atm2a(EUCOMM)Wtsi/Tbc1d10atm2a(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
increased chromosomal stability
|
J:213427
|
Tbc1d10ctm1.2Psou/Tbc1d10ctm1.2Psou
(involves: 129S2/SvPas * C57BL/6J)
|
increased T cell proliferation
|
J:211913
|
Tbc1d15em1Jren/Tbc1d15em1Jren A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: C57BL/6N * FVB/N)
|
abnormal intracellular organelle morphology
|
J:341775
|
abnormal mitochondrial physiology
|
J:341775
|
Tbc1d20bs/Tbc1d20bs
(involves: AKR/J)
|
abnormal male germ cell morphology
|
J:8222
|
abnormal sperm head morphology
|
J:8222
|
absent acrosome
|
J:8222
|
immotile sperm
|
J:8222
|
oligozoospermia
|
J:8222,
J:7104
|
teratozoospermia
|
J:8222
|
Tbc1d20bs/Tbc1d20bs
(129S;AKR-Tbc1d20bs/J)
|
abnormal cell morphology
|
J:206668
|
abnormal Golgi apparatus morphology
|
J:206668
|
absent acrosome
|
J:206668
|
decreased male germ cell number
|
J:206668
|
Tbc1d20em1Djsi/Tbc1d20em1Djsi
(involves: C57BL/6 * DBA/2)
|
abnormal acrosome assembly
|
J:315009
|
abnormal cell morphology
|
J:315009
|
Tbc1d21em1Osb/Tbc1d21em1Osb
(involves: 129S2/SvPas * C57BL/6NSlc)
|
abnormal sperm midpiece morphology
|
J:302631
|
abnormal sperm mitochondrial sheath morphology
|
J:302631
|
abnormal spermatid morphology
|
J:302631
|
Tbc1d21tm1.1Yhln/Tbc1d21tm1.1Yhln
(involves: C57BL/6)
|
abnormal mitochondrial shape
|
J:299845
|
abnormal outer dense fiber morphology
|
J:299845
|
abnormal sperm axoneme morphology
|
J:299845
|
abnormal sperm flagellum morphology
|
J:299845
|
abnormal sperm midpiece morphology
|
J:299845
|
abnormal sperm mitochondrial morphology
|
J:299845
|
abnormal sperm mitochondrial sheath morphology
|
J:299845
|
decreased mitochondrial number
|
J:299845
|
decreased sperm progressive motility
|
J:299845
|
oligozoospermia
|
J:299845
|
teratozoospermia
|
J:299845
|
Tbc1d24tm1b(EUCOMM)Hmgu/Tbc1d24+
(B6J.B6N-Tbc1d24tm1b(EUCOMM)Hmgu)
|
abnormal axon extension
|
J:271632
|
abnormal endocytosis
|
J:271632
|
increased cellular sensitivity to oxidative stress
|
J:271632
|
Tbc1d25Gt(IST10205D5)Tigm/Y
(involves: C57BL/6N)
|
cardiac interstitial fibrosis
|
J:295960
|
Tbpl1tm1Rgr/Tbpl1tm1Rgr
(involves: C57BL/6)
|
abnormal acrosome morphology
|
J:69502
|
abnormal spermatid morphology
|
J:69502
|
azoospermia
|
J:69502
|
decreased elongated spermatid number
|
J:69502
|
increased male germ cell apoptosis
|
J:69502
|
multinucleated giant male germ cells
|
J:69502
|
Tbpl1tm1Saco/Tbpl1+
(involves: 129S2/SvPas * C57BL/6)
|
oligozoospermia
|
J:68789
|
Tbpl1tm1Saco/Tbpl1tm1Saco
(involves: 129S2/SvPas * C57BL/6)
|
azoospermia
|
J:68789
|
decreased germ cell number
|
J:68789
|
increased male germ cell apoptosis
|
J:68789
|
Tbpl2tm1.1Lzt/Tbpl2tm1.1Lzt
(involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ)
|
abnormal granulosa cell apoptosis
|
J:152449
|
abnormal oocyte morphology
|
J:152449
|
absent zona pellucida
|
J:152449
|
oocyte degeneration
|
J:152449
|
Tbx1nmf219/Tbx1nmf219
(C57BL/6J-Tbx1nmf219/J)
|
abnormal organ of Corti supporting cell differentiation
|
J:278988
|
Tbx1tm1Bem/Tbx1+
(involves: 129/Sv * C57BL/6J * FVB * SJL)
|
abnormal neuron differentiation
|
J:89188
|
Tbx1tm1Bem/Tbx1tm1Bem
(involves: 129/Sv * C57BL/6J * FVB * SJL)
|
abnormal neuron differentiation
|
J:89188
|
Tbx1tm1Bld/Tbx1+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
increased vascular smooth muscle cell proliferation
|
J:212881
|
Tbx1tm1Bld/Tbx1tm1Bld
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal neural crest cell migration
|
J:76173
|
Tbx1tm1Bld/Tbx1tm1Bld
(involves: 129S7/SvEvBrd)
|
increased apoptosis
|
J:159824
|
Tbx1tm1Pa/Tbx1tm1Pa
(involves: 129 * C57BL/6)
|
abnormal neural crest cell migration
|
J:96463
|
Tbx4tm1.1Pa/Tbx4tm1.1Pa
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal vascular regression
|
J:83256
|
increased allantois apoptosis
|
J:83256
|
Tbx4tm1Pa/Tbx4tm1Pa
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal vascular regression
|
J:83256
|
increased allantois apoptosis
|
J:83256
|
Tbx6tm1Pa/Tbx6tm2Pa
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * ICR)
|
abnormal motile primary cilium morphology
|
J:137163
|
Tbx6tm2Pa/Tbx6tm2Pa Tg(CAG-GFP/MAPT)1Pa/?
(involves: 129 * 129S1/Sv * 129X1/SvJ * ICR)
|
abnormal motile primary cilium physiology
|
J:137163
|
decreased embryonic cilium length
|
J:137163
|
Tbx20tm1.1Rph/Tbx20tm1.1Rph
(involves: C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:98489
|
Tbx20tm1.1Sev/Tbx20tm1.1Sev
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:98516
|
Tbx20tm1Akis/Tbx20tm1Akis
(involves: 129S1/SvImJ * NMRI)
|
abnormal fetal cardiomyocyte proliferation
|
J:98806
|
Tbx21tm1Glm/Tbx21tm1Glm
(involves: 129S6/SvEvTac)
|
abnormal leukocyte migration
|
J:163822
|
Tbx22tm1.1Sta/Y
(involves: 129/Sv * CD-1)
|
abnormal osteoblast differentiation
|
J:153100
|
Tbx22tm1.1Sta/Tbx22tm1.1Sta
(involves: 129 * CD-1)
|
abnormal osteoblast differentiation
|
J:153100
|
Tcaptm1Rnk/Tcaptm1Rnk
(Not Specified)
|
increased cardiomyocyte apoptosis
|
J:188832
|
Tcf3tm1Xhsu/Tcf3tm1Xhsu Tg(Lck-Stat5b*)1Mafa/0
(involves: 129X1/SvJ * C57BL/6 * FVB/N)
|
increased B cell proliferation
|
J:132669
|
Tcf3tm2Cmu/Tcf3tm2Cmu
(involves: 129P2/OlaHsd)
|
abnormal cell death
|
J:118827
|
increased cell proliferation
|
J:118827
|
Tcf7l1tm1.1Efu/Tcf7l1tm1.1Efu Tcf7l2tm1Cle/Tcf7l2tm1Cle Tg(KRT14-cre)1Efu/0
(involves: 129/Sv * 129P2/OlaHsd)
|
decreased keratinocyte proliferation
|
J:155012
|
Tcf7l2tm1.1(EGFP/cre)Mrc/Tcf7l2tm1.1(EGFP/cre)Mrc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal colon goblet cell morphology
|
J:170088
|
abnormal enterocyte proliferation
|
J:170088
|
abnormal small intestine goblet cell morphology
|
J:170088
|
Tcf7l2tm1.1(EGFP/cre)Mrc/Tcf7l2tm2.1Mrc
(involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6NCrl)
|
abnormal enterocyte proliferation
|
J:170088
|
abnormal intestinal goblet cell morphology
|
J:170088
|
Tcf7l2tm1.1(EGFP/cre)Mrc/Tcf7l2tm2.2Mrc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal enterocyte proliferation
|
J:170088
|
abnormal intestinal goblet cell morphology
|
J:170088
|
Tcf7l2tm1Cle/Tcf7l2tm1Cle
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:98680
|
Tcf7l2tm2.1Cle/Tcf7l2tm2.1Cle Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
abnormal enterocyte proliferation
|
J:185753
|
abnormal small intestine goblet cell morphology
|
J:185753
|
increased enterocyte apoptosis
|
J:185753
|
Tcf7l2tm2.2Mrc/Tcf7l2tm2.2Mrc
(involves: 129S1/Sv)
|
abnormal enterocyte proliferation
|
J:170088
|
abnormal intestinal goblet cell morphology
|
J:170088
|
Tcf12tm3Zhu/Tcf12tm3Zhu Tcf3tm4Zhu/Tcf3tm4Zhu Tg(Lck-cre)#Zhu/0
(involves: 129S4/SvJae * C57BL/6 * SJL/J)
|
increased T cell proliferation
|
J:129570
|
Tcf23em1Hoi/Tcf23em1Hoi
(C57BL/6N-Tcf23em1Hoi)
|
abnormal cell adhesion
|
J:354446
|
abnormal extracellular matrix morphology
|
J:354446
|
Tcfl5tm1.1Frem/Tcfl5tm1.1Frem
(involves: C57BL/6 * CBA)
|
abnormal chiasmata formation
|
J:326601
|
arrest of male meiosis
|
J:326601
|
azoospermia
|
J:326601
|
increased male germ cell apoptosis
|
J:326601
|
multinucleated giant male germ cells
|
J:326601
|
Tcfl5tm1Frem/Tcfl5tm1Frem Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * CBA)
|
abnormal spermatid morphology
|
J:326601
|
arrest of male meiosis
|
J:326601
|
azoospermia
|
J:326601
|
multinucleated giant male germ cells
|
J:326601
|
Tchptm1Inag/Tchptm1Inag
(B6.129P2-Tchptm1Inag)
|
abnormal fat cell differentiation
|
J:304307
|
Tcirg1tm1.1Ywd/?
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
cellular phenotype
|
J:150327
|
Tcof1tm1Mjd/Tcof1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal neural crest cell migration
|
J:89223
|
increased neural tube apoptosis
|
J:62928
|
Tcof1tm1Mjd/Tcof1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/1)
|
abnormal cranial neural crest cell migration
|
J:112900
|
decreased cranial neural crest cell proliferation
|
J:112900
|
increased embryonic neuroepithelium apoptosis
|
J:112900
|
Tcof1tm1Mjd/Tcof1+
(involves: 129S1/Sv * 129X1/SvJ * CBA/Ca)
|
abnormal neural crest cell migration
|
J:89223
|
Tcra-Jtm1Tgi/Tcra-Jtm1Tgi
(B6.129-Tcra-Jtm1Tgi)
|
decreased hepatocyte apoptosis
|
J:135830
|
Tcratm1Mjo/Tcratm1Mjo
(involves: 129P2/OlaHsd)
|
abnormal neuron proliferation
|
J:170591
|
decreased T cell proliferation
|
J:110898
|
Tcratm1Mom/Tcratm1Mom
(involves: 129S2/SvPas * C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:15221
|
Tcratm1Mom/Tcratm1Mom Tcrgtm1.1Hish/Tcrgtm1.1Hish
(involves: 129P2/OlaHsd * 129S2/SvPas * C57BL/6)
|
impaired macrophage chemotaxis
|
J:135597
|
Tcrbtm1Mom/Tcrbtm1Mom Tcrdtm1Mom/Tcrdtm1Mom Traf3ip2tm1.1Lix/Traf3ip2tm1.1Lix
(B6.129-Tcrbtm1Mom Traf3ip2tm1.1Lix Tcrdtm1Mom)
|
increased mesangial cell number
|
J:187766
|
Tcrdtm1Mom/Tcrdtm1Mom
(B6.129P2-Tcrdtm1Mom)
|
increased apoptosis
|
J:94872
|
Tcte1tm1a(KOMP)Wtsi/Tcte1tm1a(KOMP)Wtsi
(C57BL/6N-Tcte1tm1a(KOMP)Wtsi)
|
abnormal gametes
|
J:243766
|
abnormal sperm flagellum morphology
|
J:243766
|
asthenozoospermia
|
J:243766
|
Tctn1Gt(KST296)Byg/Tctn1Gt(KST296)Byg
(involves: 129P2/OlaHsd)
|
absent embryonic cilia
|
J:176174
|
cellular phenotype
|
J:176174
|
Tctn2tm1.1Reit/Tctn2tm1.1Reit
(involves: 129P2/OlaHsd * C57BL/6)
|
absent embryonic cilia
|
J:176174
|
Tctn3tm1.2Blnw/Tctn3tm1.2Blnw
(involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SW)
|
abnormal cilium morphology
|
J:249241
|
decreased embryonic neuroepithelium primary cilium number
|
J:249241
|
Tctn3tm2(Tctn1)Blnw/Tctn3tm2(Tctn1)Blnw
(involves: 129S6/SvEvTac * C57BL/6 * SW)
|
abnormal cilium morphology
|
J:249241
|
decreased embryonic neuroepithelium primary cilium number
|
J:249241
|
Tctn3tm3(Tctn2)Blnw/Tctn3tm3(Tctn2)Blnw
(involves: 129S6/SvEvTac * C57BL/6 * SW)
|
abnormal cilium morphology
|
J:249241
|
decreased embryonic neuroepithelium primary cilium number
|
J:249241
|
Tdgtm1.1Abc/Tdgtm1.1Abc
(B6.129-Tdgtm1.1Abc)
|
abnormal DNA methylation
|
J:174772
|
abnormal mismatch repair
|
J:174772
|
Tdgtm2.1Abc/Tdgtm2.1Abc
(B6.129-Tdgtm2.1Abc)
|
abnormal DNA methylation
|
J:174772
|
Tdo2tm1Tnak/Tdo2tm1Tnak
(B6.129-Tdo2tm1Tnak)
|
abnormal neuron differentiation
|
J:177903
|
abnormal neuronal precursor proliferation
|
J:177903
|
Tdp1Gt(XD105)Byg/Tdp1Gt(XD105)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal single-strand DNA break repair
|
J:127605
|
Tdp1Gt(XD105)Byg/Tdp1Gt(XD105)Byg
(involves: 129P2/OlaHsd)
|
abnormal DNA repair
|
J:170077
|
Tdp2tm1.1Huy/Tdp2tm1.1Huy
(involves: 129P2/OlaHsd * CD-1)
|
abnormal cell nucleus morphology
|
J:195301
|
abnormal chromosome morphology
|
J:195301
|
abnormal mitosis
|
J:195301
|
Tdrd1tm1Chum/Tdrd1tm1Chum
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal chromatoid body morphology
|
J:115333
|
abnormal oocyte morphology
|
J:115333
|
abnormal spermatid morphology
|
J:115333
|
abnormal spermatocyte morphology
|
J:115333
|
azoospermia
|
J:115333
|
increased male germ cell apoptosis
|
J:115333
|
Tdrd3Gt(RRK474)Byg/Tdrd3Gt(RRK474)Byg
(involves: 129P2/OlaHsd)
|
chromosomal instability
|
J:210647
|
Tdrd5tm1Sait/Tdrd5tm1Sait
(involves: C57BL/6 * CBA)
|
abnormal acrosome morphology
|
J:170319
|
abnormal cell physiology
|
J:170319
|
abnormal male germ cell apoptosis
|
J:170319
|
abnormal spermatocyte morphology
|
J:170319
|
arrest of male meiosis
|
J:170319
|
globozoospermia
|
J:170319
|
Tdrd6tm1Jess/Tdrd6tm1Jess
(either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal cell morphology
|
J:148942
|
azoospermia
|
J:148942
|
increased male germ cell apoptosis
|
J:148942
|
Tdrd7tm1.1Chum/Tdrd7tm1.1Chum
(involves: 129S6/SvEvTac * C57BL/6)
|
increased male germ cell apoptosis
|
J:173550
|
Tdrd9tm1.1Chum/Tdrd9tm1.1Chum
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal DNA methylation during gametogenesis
|
J:156018
|
abnormal male germ cell morphology
|
J:156018
|
abnormal spermatocyte morphology
|
J:156018
|
abnormal spermatogonia morphology
|
J:156018
|
abnormal synaptonemal complex
|
J:156018
|
arrest of male meiosis
|
J:156018
|
azoospermia
|
J:156018
|
increased male germ cell apoptosis
|
J:156018
|
Tdrd12repro23/Tdrd12repro23
(involves: C3HeB/FeJ * C57BL/6J)
|
abnormal male germ cell morphology
|
J:166101
|
arrest of male meiosis
|
J:92463
|
azoospermia
|
J:166101,
J:92463
|
decreased spermatid number
|
J:166101
|
Tdrd12tm1Yam/Tdrd12tm1Yam
(involves: 129S4/SvJae * C57BL/6)
|
azoospermia
|
J:202012
|
decreased round spermatid number
|
J:202012
|
Tdrkhtm1.2Hfl/Tdrkhtm1.2Hfl
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N)
|
abnormal cell physiology
|
J:197673
|
abnormal DNA methylation
|
J:197673
|
abnormal double-strand DNA break repair
|
J:197673
|
abnormal synaptonemal complex
|
J:197673
|
arrest of male meiosis
|
J:197673
|
azoospermia
|
J:197673
|
Tdrptm1Xwa/Tdrptm1Xwa
(involves: 129 * C57BL/6)
|
abnormal sperm head morphology
|
J:307459
|
abnormal sperm motility
|
J:307459
|
decreased sperm progressive motility
|
J:307459
|
Tead1tm1Hssk/Tead1tm1Hssk Tead2tm1Hssk/Tead2tm1Hssk
(either: (involves: C57BL/6 * CBA) or (involves: C57BL/6 * CBA * CD-1))
|
decreased cell proliferation
|
J:131426
|
increased embryonic tissue cell apoptosis
|
J:131426
|
Tecpr1tm1Chsa/Tecpr1tm1Chsa
(involves: 129S4/SvJae)
|
abnormal autophagy
|
J:198333
|
Tecpr2em1Wei/Tecpr2em1Wei
(C57BL/6J-Tecpr2em1Wei)
|
impaired autophagy
|
J:304963
|
Tecrlem1Bcgen/Tecrlem1Bcgen
(C57BL/6-Tecrlem1Bcgen)
|
abnormal cellular respiration
|
J:325991
|
abnormal myocardial fiber mitochondrial morphology
|
J:325991
|
oxidative stress
|
J:325991
|
Tefmtm1.1Lrsn/Tefmtm1.1Lrsn Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6N * FVB)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:276874
|
abnormal mitochondrial morphology
|
J:276874
|
increased mitochondrial DNA content
|
J:276874
|
Tekt2Gt(OST12401)Lex/Tekt2Gt(OST12401)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal respiratory motile cilium morphology
|
J:92779
|
abnormal respiratory motile cilium physiology
|
J:92779
|
abnormal sperm axoneme morphology
|
J:92779
|
asthenozoospermia
|
J:92779
|
hairpin sperm flagellum
|
J:92779
|
Tekt3tm1Zuk/Tekt3tm1Zuk
(either: 129S7/SvEvBrd-Tekt3tm1Zuk or (involves: 129S7/SvEvBrd * C57BL/6J))
|
asthenozoospermia
|
J:148050
|
hairpin sperm flagellum
|
J:148050
|
Tekt3tm1Zuk/Tekt3tm1Zuk Tekt4tm1Zuk/Tekt4tm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
asthenozoospermia
|
J:148050
|
Tekt4tm1Zuk/Tekt4tm1Zuk
(involves: 129S5/SvEvBrd * 129S7/SvEvBrd)
|
abnormal sperm fibrous sheath morphology
|
J:134732
|
abnormal sperm flagellum morphology
|
J:134732
|
abnormal sperm midpiece morphology
|
J:134732
|
asthenozoospermia
|
J:134732
|
Telo2tm1Tdl/Telo2tm1.1Tdl Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129 * 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle
|
J:141633
|
abnormal DNA repair
|
J:141633
|
early cellular replicative senescence
|
J:141633
|
Telo2tm1Tdl/Telo2tm1.1Tdl Trp53tm1Tyj/Trp53tm1Tyj Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129 * 129P2/OlaHsd * 129S2/SvPas * C57BL/6J)
|
abnormal cell cycle
|
J:141633
|
Tenm4Tg(Col2a1-Hspg2)2Yoya/Tenm4Tg(Col2a1-Hspg2)2Yoya
(C57BL/6-Tenm4Tg(Col2a1-Hspg2)2Yoya)
|
abnormal oligodendrocyte apoptosis
|
J:187705
|
Tent2tm1Tomo/Tent2tm1Tomo
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cell physiology
|
J:128466
|
Tent5bem1Adki/Tent5bem1Adki Tent5cem1Adki/Tent5cem1Adki
(involves: C57BL/6JTar * CBA/WTar)
|
abnormal oogenesis
|
J:360869
|
increased female germ cell apoptosis
|
J:360869
|
increased granulosa cell apoptosis
|
J:360869
|
increased ovary apoptosis
|
J:360869
|
oocyte degeneration
|
J:360869
|
Tent5bem3Adki/Tent5b+
(involves: C57BL/6JTar * CBA/WTar)
|
abnormal female meiosis
|
J:360869
|
parthenogenesis
|
J:360869
|
Tent5bem3Adki/Tent5bem3Adki
(involves: C57BL/6JTar * CBA/WTar)
|
abnormal female meiosis
|
J:360869
|
Tent5cem1Adki/Tent5cem1Adki
(involves: C57BL/6JTar * CBA/WTar)
|
abnormal sperm head morphology
|
J:360869
|
arrest of male meiosis
|
J:360869
|
decreased B cell proliferation
|
J:252302
|
decreased male germ cell number
|
J:360869
|
increased male germ cell apoptosis
|
J:360869
|
Tent5cem1Hncs/Tent5cem1Hncs
(involves: C57BL/6J * DBA)
|
abnormal sperm connecting piece morphology
|
J:277640
|
abnormal sperm nucleus morphology
|
J:277640
|
absent sperm head
|
J:277640
|
oligozoospermia
|
J:277640
|
Tent5dem1Adki/Y
(involves: C57BL/6JTar * CBA/WTar)
|
increased male germ cell apoptosis
|
J:360869
|
Tent5dem1Fzh/Y
(involves: C57BL/6)
|
asthenozoospermia
|
J:338795
|
globozoospermia
|
J:338795
|
increased male germ cell apoptosis
|
J:338795
|
multinucleated giant male germ cells
|
J:338795
|
oligozoospermia
|
J:338795
|
Terb1tm1a(KOMP)Mbp/Terb1tm1a(KOMP)Mbp
(C57BL/6-Terb1tm1a(KOMP)Mbp)
|
abnormal female meiosis
|
J:205574
|
abnormal female meiosis I arrest
|
J:205574
|
abnormal male meiosis
|
J:205574
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:205574
|
absent oocytes
|
J:205574
|
arrest of male meiosis
|
J:205574
|
azoospermia
|
J:205574
|
increased male germ cell apoptosis
|
J:205574
|
Terb2em1Leim/Terb2em1Leim
(C57BL/6-Terb2em1Leim)
|
abnormal double-strand DNA break repair
|
J:270644
|
abnormal female meiosis
|
J:270644
|
abnormal synaptonemal complex
|
J:270644
|
arrest of male meiosis
|
J:270644
|
azoospermia
|
J:270644
|
increased male germ cell apoptosis
|
J:270644
|
Terb2em2Leim/Terb2em2Leim
(C57BL/6-Terb2em2Leim)
|
abnormal double-strand DNA break repair
|
J:270644
|
abnormal female meiosis
|
J:270644
|
abnormal synaptonemal complex
|
J:270644
|
arrest of male meiosis
|
J:270644
|
azoospermia
|
J:270644
|
increased male germ cell apoptosis
|
J:270644
|
Terctm1Rdp/Terctm1Rdp
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal chromosome morphology
|
J:89751
|
abnormal female meiosis
|
J:89751
|
abnormal fetal cardiomyocyte proliferation
|
J:110900
|
abnormal male meiosis
|
J:89751
|
abnormal meiosis
|
J:89751
|
abnormal oocyte morphology
|
J:89751
|
abnormal spermatocyte morphology
|
J:89751
|
abnormal telomere length
|
J:74001,
J:89751,
J:120065,
J:43517,
J:60223,
J:110900,
J:96945
|
decreased B cell proliferation
|
J:60223
|
decreased T cell proliferation
|
J:60223
|
increased apoptosis
|
J:120065
|
increased B cell apoptosis
|
J:60223
|
increased cardiomyocyte apoptosis
|
J:110900
|
increased embryonic tissue cell apoptosis
|
J:53600
|
increased male germ cell apoptosis
|
J:89751,
J:120065
|
Terctm1Rdp/Terctm1Rdp
(involves: FVB/N)
|
abnormal telomere length
|
J:98586
|
decreased elongated spermatid number
|
J:98586
|
Terctm1Rdp/Terctm1Rdp
(involves: 129/Sv * C57BL/6 * C57BL/6J * SJL)
|
abnormal cell physiology
|
J:125218
|
abnormal DNA repair
|
J:125218
|
abnormal enterocyte proliferation
|
J:125218
|
chromosomal instability
|
J:125218
|
decreased telomere length
|
J:125218
|
increased enterocyte apoptosis
|
J:125218
|
Terctm1Rdp/Terctm1Rdp Tg(KRT5-Terf2)PMBlas/Y
(involves: 129/Sv * C57BL/6 * CBA * SJL)
|
decreased telomere length
|
J:102653
|
Terctm1Rdp/Terctm1Rdp Tg(KRT5-Tert)8043Blas/0
(involves: 129/Sv * C57BL/6 * C57BL/6J * DBA/2 * SJL)
|
abnormal chromosome morphology
|
J:96945
|
decreased telomere length
|
J:96945
|
Terctm1Rdp/Terctm1Rdp Tinf2tm2.2Tdl/Tinf2+
(involves: 129 * BALB/cJ * C57BL/6 * SJL)
|
abnormal chromosome morphology
|
J:207367
|
decreased telomere length
|
J:207367
|
Terctm1Rdp/Terctm1Rdp Wrntm1Lgu/Wrntm1Lgu
(involves: 129/Sv * BALB/c * C57BL/6 * SLJ)
|
abnormal chromosome morphology
|
J:91715
|
decreased telomere length
|
J:91715
|
Terf1tm1.1Blas/Terf1tm1.1Blas
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL)
|
abnormal chromosome morphology
|
J:152077
|
abnormal telomere length
|
J:152077
|
decreased cell proliferation
|
J:152077
|
early cellular replicative senescence
|
J:152077
|
Terf1tm1.1Blas/Terf1tm1.1Blas Tg(KRT5-cre)1Tak/0
(involves: 129 * C3H * C57BL/6 * SJL)
|
abnormal chromosome morphology
|
J:152077
|
abnormal telomere length
|
J:152077
|
Terf1tm1Tdl/Terf1tm1Tdl
(involves: 129S2/SvPas)
|
abnormal inner cell mass apoptosis
|
J:85440
|
absent inner cell mass proliferation
|
J:85440
|
Terf1tm2.1Tdl/Terf1tm2.1Tdl
(involves: 129P2/OlaHsd * C57BL/6)
|
early cellular replicative senescence
|
J:157331
|
Terf2tm1Tdl/Terf2tm1.1Tdl Tg(Mx1-cre)1Cgn/0
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal chromosome morphology
|
J:112957
|
Terf2iptm1.1Blas/Terf2iptm1.1Blas
(involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL)
|
abnormal telomere morphology
|
J:165984
|
cellular phenotype
|
J:165984
|
decreased telomere length
|
J:165984
|
increased chromosomal stability
|
J:165984
|
Terf2iptm1.1Blas/Terf2iptm1.1Blas Tg(KRT5-cre)1Tak/0
(involves: 129S2/SvPas * C3H * C57BL/6 * SJL)
|
abnormal telomere morphology
|
J:165984
|
Terf2iptm1.2Tdl/Terf2iptm1.2Tdl
(involves: C57BL/6J * FVB/N)
|
cellular phenotype
|
J:158884,
J:199372
|
Terttm1.1Phan/Terttm1.1Phan Tg(Col1a2-cre/ERT,-ALPP)7Cpd/0
(involves: C57BL/6 * DBA/2)
|
decreased lung fibroblast proliferation
|
J:239734
|
increased apoptosis
|
J:239734
|
Terttm1Leah/Tert+
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal telomere length
|
J:90866
|
aneuploidy
|
J:90866
|
Terttm1Leah/Terttm1Leah
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal telomere length
|
J:90866
|
aneuploidy
|
J:90866
|
chromosomal instability
|
J:90866
|
Terttm1Rdp/Terttm1Rdp
(B6.Cg-Terttm1Rdp)
|
abnormal chromosome morphology
|
J:108914
|
decreased telomere length
|
J:108914
|
increased apoptosis
|
J:108914
|
Terttm1Sear/Terttm1Sear
(involves: 129S4/SvJae * C57BL/6)
|
abnormal telomere length
|
J:127153
|
increased apoptosis
|
J:127153
|
Terttm1Yjc/Tert+
(involves: C57BL/6 * SPRET/Ei)
|
cellular phenotype
|
J:92243
|
Terttm1Yjc/Terttm1Yjc
(involves: C57BL/6 * SPRET/Ei)
|
abnormal telomere length
|
J:92243
|
Terttm1Yjc/Terttm1Yjc
(involves: 129/Sv * C57BL/6 * SJL * SPRET/Ei)
|
abnormal telomere length
|
J:92243
|
Terttm2.1Rdp/Terttm2.1Rdp
(involves: C57BL/6)
|
abnormal chromosome morphology
|
J:167227
|
abnormal male germ cell apoptosis
|
J:167227
|
abnormal neuron differentiation
|
J:167227
|
abnormal neuronal precursor proliferation
|
J:167227
|
decreased telomere length
|
J:167227
|
early cellular replicative senescence
|
J:167227
|
Terttm3Rdp/Terttm3Rdp
(involves: C57BL/6)
|
decreased cell proliferation
|
J:186105
|
increased apoptosis
|
J:186105
|
increased small intestinal crypt cell apoptosis
|
J:186105
|
Teshlem1Choc/Teshlem1Choc
(C57BL/6-1700027A15Rikem1Choc)
|
abnormal sperm head morphology
|
J:307510
|
Tesminem1Osb/Tesminem1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
arrest of male meiosis
|
J:288964
|
Tesminem1Qsh/Tesminem1Qsh
(involves: C57BL/6J)
|
abnormal spermatocyte morphology
|
J:324057
|
arrest of male meiosis
|
J:324057
|
azoospermia
|
J:324057
|
increased male germ cell apoptosis
|
J:324057
|
Tesminem2Qsh/Tesminem2Qsh
(involves: C57BL/6J)
|
abnormal spermatocyte morphology
|
J:324057
|
arrest of male meiosis
|
J:324057
|
azoospermia
|
J:324057
|
increased male germ cell apoptosis
|
J:324057
|
Tespa1tm1Smoc/Tespa1tm1Smoc
(B6.129-Tespa1tmSmoc)
|
decreased T cell proliferation
|
J:186446
|
increased T cell proliferation
|
J:186446
|
Tet1Gt(RRG140)Byg/Tet1Gt(RRG140)Byg
(B6.129P2-Tet1Gt(RRG140)Byg)
|
abnormal double-strand DNA break repair
|
J:194101
|
abnormal female meiosis
|
J:194101
|
abnormal synaptonemal complex
|
J:194101
|
decreased oocyte number
|
J:194101
|
increased female germ cell apoptosis
|
J:194101
|
increased ovary apoptosis
|
J:194101
|
Tet1tm1.1Gxu/Tet1tm1.1Gxu Tg(Nes-EGFP)33Enik/0
(involves: 129 * BALB/cBy * C57BL/6 * C57BL/6J)
|
abnormal DNA methylation
|
J:201001
|
abnormal neuronal precursor proliferation
|
J:201001
|
Tet1tm1Gxu/Tet1tm1.1Gxu Tg(Nes-cre/ERT2)KEisc/0
(involves: 129 * C57BL/6J)
|
abnormal neuron differentiation
|
J:201001
|
abnormal neuronal precursor proliferation
|
J:201001
|
Tet1tm1Gxu/Tet1tm1Gxu
(involves: 129 * C57BL/6J)
|
abnormal neuronal precursor proliferation
|
J:201001
|
Tet2Gt(AN0709)Wtsi/Tet2+
(B6.129P2-Tet2Gt(AN0709)Wtsi)
|
abnormal monocyte differentiation
|
J:174052
|
Tet2Gt(AN0709)Wtsi/Tet2Gt(AN0709)Wtsi
(B6.129P2-Tet2Gt(AN0709)Wtsi)
|
abnormal monocyte differentiation
|
J:174052
|
Tet3tm1.1Gxu/Tet3tm1.2Gxu Tg(Zp3-cre)3Mrt/0
(involves: 129 * C57BL/6J * FVB/N * SJL)
|
abnormal DNA methylation
|
J:176196
|
maternal effect
|
J:176196
|
Tex10tm1(KOMP)Vlcg/Tex10tm1(KOMP)Vlcg
(involves: C57BL/6NTac)
|
decreased inner cell mass proliferation
|
J:224684
|
Tex11tm1.1Jpt/Y
(involves: 129/Sv * C57BL/6 * CD-1)
|
abnormal male meiosis
|
J:136834
|
Tex11tm1Jw/Y Tmem163Tg(ACTB-cre)2Mrt/0
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal chiasmata formation
|
J:131722
|
arrest of male meiosis
|
J:131722
|
increased male germ cell apoptosis
|
J:131722
|
meiotic nondisjunction during M1 phase
|
J:131722
|
Tex11tm1Jw/Tex11tm1Jw Tmem163Tg(ACTB-cre)2Mrt/0
(involves: 129S4/SvJae * C57BL/6 * FVB/N)
|
abnormal chiasmata formation
|
J:131722
|
Tex12tm1Hoog/Tex12tm1Hoog
(involves: 129S2/SvPas)
|
abnormal chiasmata formation
|
J:139993
|
abnormal female meiosis
|
J:139993
|
abnormal male meiosis
|
J:139993
|
decreased oocyte number
|
J:139993
|
oocyte degeneration
|
J:139993
|
Tex14tm1Zuk/Tex14tm1Zuk
(129S/SvEv-Tex14tm1Zuk)
|
abnormal spermatocyte morphology
|
J:107660
|
arrest of male meiosis
|
J:107660
|
Tex14tm1Zuk/Tex14tm1Zuk
(either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J))
|
arrest of male meiosis
|
J:107660
|
Tex15tm1Jw/Tex15tm1Jw
(involves: 129S4/SvJae * C57BL/6)
|
abnormal double-strand DNA break repair
|
J:135578
|
arrest of male meiosis
|
J:135578
|
decreased male germ cell number
|
J:135578
|
Tex19.1tm1(rtTA2S*M2,lacZ)Jw/Tex19.1tm1(rtTA2S*M2,lacZ)Jw
(involves: 129S4/SvJae * C57BL/6)
|
abnormal chiasmata formation
|
J:166982
|
arrest of male meiosis
|
J:166982
|
Tex19.1tm1.2Ics/Tex19.1tm1.2Ics
(involves: C57BL/6)
|
arrest of male meiosis
|
J:198685
|
asthenozoospermia
|
J:198685
|
azoospermia
|
J:198685
|
increased male germ cell apoptosis
|
J:198685
|
oligozoospermia
|
J:198685
|
teratozoospermia
|
J:198685
|
Tex19.1tm1Hjc/Tex19.1tm1Hjc
(involves: 129P2/OlaHsd * CD-1)
|
abnormal male meiosis
|
J:159793
|
decreased male germ cell number
|
J:159793
|
increased male germ cell apoptosis
|
J:159793
|
oligozoospermia
|
J:159793
|
Tex19.1tm2.2Ics/Tex19.1tm2.2Ics Tex19.2tm1.2Ics/Tex19.2tm1.2Ics
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal synaptonemal complex
|
J:243444
|
arrest of male meiosis
|
J:243444
|
azoospermia
|
J:243444
|
Tex44em1Sbbx/Tex44em1Sbbx
(C57BL/6N-Tex44em1Sbbx)
|
abnormal mitochondrial physiology
|
J:354514
|
abnormal outer dense fiber morphology
|
J:354514
|
abnormal sperm axoneme morphology
|
J:354514
|
abnormal sperm flagellum morphology
|
J:354514
|
abnormal sperm mitochondrial morphology
|
J:354514
|
abnormal sperm principal piece morphology
|
J:354514
|
asthenozoospermia
|
J:354514
|
hairpin sperm flagellum
|
J:354514
|
Tex46em1Ncvc/Tex46em1Ncvc
(involves: C57BL/6 * DBA/2)
|
abnormal acrosome morphology
|
J:355678
|
abnormal sperm head morphology
|
J:355678
|
asthenozoospermia
|
J:355678
|
detached acrosome
|
J:355678
|
kinked sperm flagellum
|
J:355678
|
Tex101tm1Osb/Tex101tm1Osb Tg(CAG-EGFP,Acr-EGFP)2Osb/Tg(CAG-EGFP,Acr-EGFP)2Osb
(involves: C57BL/6NSlc)
|
abnormal hyperactivated sperm motility
|
J:197323
|
impaired sperm migration in female genital tract
|
J:197323
|
Tex101tm1Qzh/Tex101tm1Qzh
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * ICR))
|
impaired sperm migration in female genital tract
|
J:208737
|
Tfamtm1.1Lrsn/Tfamtm1.1Lrsn
(involves: 129S1/Sv * 129X1/SvJ * FVB/N)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:125471
|
decreased mitochondrial DNA content
|
J:46387
|
disorganized mitochondrial cristae
|
J:46387
|
increased apoptosis
|
J:125471
|
increased mitochondrial size
|
J:46387
|
Tfamtm1.1Ncdl/Tfamtm1.1Ncdl Tg(KRT14-cre)1Amc/0
(involves: C57BL/6 * CBA)
|
abnormal keratinocyte differentiation
|
J:213840
|
abnormal mitochondrial physiology
|
J:213840
|
abnormal redox activity
|
J:213840
|
increased keratinocyte proliferation
|
J:213840
|
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Camk2a-cre)1Lfr/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA)
|
abnormal respiratory electron transport chain
|
J:72037
|
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Ckmm-cre)1Lrsn/0
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal respiratory electron transport chain
|
J:125471
|
increased cardiomyocyte apoptosis
|
J:125471
|
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Ins2-cre)25Mgn/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA)
|
abnormal mitochondrial morphology
|
J:65522
|
abnormal respiratory electron transport chain
|
J:65522
|
decreased mitochondrial DNA content
|
J:65522
|
Tfamtm1Lrsn/Tfamtm1Lrsn Tg(Myhca-cre)1Lrsn/0
(involves: 129S1/Sv * 129X1/SvJ * FVB)
|
abnormal respiratory electron transport chain
|
J:61372
|
Tfap2atm1Hsv/Tfap2atm2Will H2az2Tg(Wnt1-cre)11Rth/H2az2+
(Not Specified)
|
cellular phenotype
|
J:88826
|
Tfap2atm1Jae/Tfap2atm1Jae
(either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c))
|
abnormal apoptosis
|
J:33032
|
Tfap2atm1Will/Tfap2atm1Will
(involves: Black Swiss)
|
abnormal cell death
|
J:33031
|
Tfap2bem1Fenli/Tfap2bem1Fenli
(involves: C57BL/6)
|
patent ductus arteriosus
|
J:278067
|
Tfap2btm1Rbu/Tfap2b+
(involves: 129S1/Sv * 129X1/SvJ)
|
patent ductus arteriosus
|
J:175832
|
Tfap2btm1Rbu/Tfap2btm1Rbu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
increased kidney apoptosis
|
J:42260
|
increased renal tubule apoptosis
|
J:42260
|
Tfap2btm1Rbu/Tfap2btm1Rbu
(involves: 129S1/Sv * 129X1/SvJ)
|
patent ductus arteriosus
|
J:175832
|
Tfap2dtm1Mos/Tfap2dtm1Mos
(Not Specified)
|
increased apoptosis
|
J:177585
|
Tfb1mtm1.2Lrsn/Tfb1mtm1.2Lrsn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N * SJL)
|
abnormal respiratory electron transport chain
|
J:148166
|
Tfb2mtm1a(KOMP)Wtsi/Tfb2m+ Tg(Ins2-cre)23Herr/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:256448
|
abnormal mitochondrial physiology
|
J:256448
|
Tfb2mtm1a(KOMP)Wtsi/Tfb2mtm1a(KOMP)Wtsi Tg(Ins2-cre)23Herr/0
(involves: C57BL/6J * C57BL/6N * CBA/J)
|
abnormal mitochondrial morphology
|
J:256448
|
abnormal mitochondrial physiology
|
J:256448
|
abnormal mitophagy
|
J:256448
|
abnormal pancreatic islet cell apoptosis
|
J:256448
|
decreased mitochondrial DNA content
|
J:256448
|
dilated mitochondrion
|
J:256448
|
impaired autophagy
|
J:256448
|
increased endoplasmic reticulum stress
|
J:256448
|
Tfrctm1Nca/Tfrctm1Nca
(either: (involves: 129S4/SvJae * 129S6/SvEvTac) or (involves: 129S4/SvJae * C57BL/6))
|
increased apoptosis
|
J:54107
|
Tfrctm3.1Nca/Tfrctm3.1Nca Tg(Vil1-cre)20Syr/0
(involves: 129S4/SvJae * C57BL/6 * CD-1 * DBA/2)
|
abnormal enterocyte proliferation
|
J:224823
|
Tfrctm3.1Nca/Tfrctm3.1Nca Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129S4/SvJae * C57BL/6 * CD-1 * DBA/2)
|
abnormal enterocyte proliferation
|
J:224823
|
Tg(ABCA1)1Hgc/?
(involves: FVB)
|
increased cholesterol efflux
|
J:118917
|
Tg(Acp5-Adam8)#Rood/0
(involves: BALB/c * C57BL/6)
|
abnormal osteoclast differentiation
|
J:172936
|
Tg(Acp5-Selenow)#Djeo/0
(involves: FVB/N)
|
abnormal osteoclast differentiation
|
J:317012
|
Tg(ACTA1-IGF1)1Rjs/0
(involves: FVB)
|
cardiac interstitial fibrosis
|
J:58354
|
X/Tg(ACTA1-STIM1)2Jmol
(involves: FVB/N)
|
abnormal mitochondrial morphology
|
J:101977
|
abnormal mitochondrial shape
|
J:101977
|
Tg(Acta2-RAC1*G12V)33Pjgc/Tg(Acta2-RAC1*G12V)33Pjgc
(involves: C57BL/6 * FVB/N)
|
aneuploidy
|
J:150015
|
oxidative stress
|
J:150015
|
polyploidy
|
J:150015
|
Tg(ACTB-APP*V717F)1Colm/0
(involves: C57BL/6 * DBA)
|
increased apoptosis
|
J:157859
|
Tg(ACTB-Eif4e)#Ppp/?
(Not Specified)
|
early cellular replicative senescence
|
J:89878
|
Tg(ACTB-Eif4e)#Ppp/0 Tg(IghMyc)22Bri/0
(involves: C57BL * SJL)
|
decreased B cell apoptosis
|
J:89878
|
Tg(ACTB-HSF1)1Anak/?
(involves: C57BL/6 * CBA)
|
arrest of male meiosis
|
J:61442
|
Tg(ACTB-NOTCH1)1Shn/0 Tg(Nes-cre)1Kln/0 Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal apoptosis
|
J:90392
|
Tg(ACTB-NOTCH1)1Shn/0 Tg(Nes-cre)1Kln/0 Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6J)
|
cellular phenotype
|
J:90392
|
Tg(ACTB-NOTCH1)1Shn/? Tg(Nes-cre/Esr1*)4Ynj/?
(involves: C57BL/6 * C57BL/6J)
|
increased neuron apoptosis
|
J:127227
|
Tg(ACTB-NOTCH1)1Shn/0 Tg(Syn1-cre)671Jxm/0
(involves: C57BL/6J)
|
cellular phenotype
|
J:90392
|
Tg(Actb-NOTCH1)2Shn/0 Tg(Nes-cre)1Kln/0
(involves: C57BL/6J * SJL)
|
abnormal apoptosis
|
J:90392
|
Tg(ACTB-SLC2A1)224Cwh/0
(B6.Cg-Tg(ACTB-SLC2A1)224Cwh)
|
increased cellular glucose import
|
J:160943
|
Tg(ACTB-TNFRSF6B)754Jwu/?
(B6.Cg-Tg(Actb-TNFRSF6B)754Jwu)
|
abnormal mesangial cell morphology
|
J:148162
|
Tg(Actb-Tnfsf4)1Nish/0
(B6.D2-Tg(Actb-Tnfsf4)1Nish)
|
increased T cell proliferation
|
J:80214
|
Tg(ACTB-Twnk)#Suom/0
(involves: FVB/N)
|
cellular phenotype
|
J:104378
|
Tg(ACTB-Twnk*)DSuom/0
(involves: FVB/N)
|
abnormal cellular respiration
|
J:104378
|
abnormal DNA repair
|
J:104378
|
abnormal mitochondrial morphology
|
J:104378
|
increased mitochondrial fission
|
J:104378
|
Tg(ACTB-Twnk*A360T)HSuom/0
(involves: FVB/N)
|
abnormal mitochondrial physiology
|
J:104378
|
Tg(Adipoq-Zc3h10)#Hsul/0
(Not Specified)
|
increased mitochondrial number
|
J:287066
|
Tg(Adipoq-Zc3h10*)#Hsul/0
(Not Specified)
|
increased mitochondrial number
|
J:287066
|
Tg(AGER)#Eca/0
(C57BL/6J-Tg(AGER)#Eca)
|
decreased lung endothelial cell proliferation
|
J:205092
|
Tg(AGER)#Eca/Tg(AGER)#Eca
(C57BL/6J-Tg(AGER)#Eca)
|
decreased lung endothelial cell proliferation
|
J:205092
|
Tg(AGT)2-5Afu/0
(involves: C57BL/6)
|
maternal effect
|
J:194606
|
Tg(Alb1-Myc)#Sst/0 Tg(MtTGFA)42Lmb/0
(involves: C57BL/6 * CBA * CD-1)
|
increased hepatocyte apoptosis
|
J:34434
|
increased hepatocyte karyomegaly
|
J:34434
|
Tg(Alb-E2F1)8Sst/0
(involves: C57BL/6J * CBA/J)
|
increased hepatocyte proliferation
|
J:65354
|
Tg(Alb-HRAS*G12V)28Yu/0
(involves: C57BL/6J * CBA/J)
|
increased hepatocyte apoptosis
|
J:107083
|
oxidative stress
|
J:107083
|
Tg(Alb-PDGFC)#Jcam/0
(involves: C57BL/6)
|
increased hepatocyte proliferation
|
J:96979
|
Tg(Alb-REG3A)24Lchr/0
(involves: C57BL/6 * CBA)
|
increased hepatocyte proliferation
|
J:140235,
J:84698
|
Tg(Alb-SREBF1_ic)#Jkot/0
(involves: C57BL/6)
|
abnormal aerobic respiration
|
J:249664
|
abnormal cellular respiration
|
J:249664
|
abnormal lipid oxidation
|
J:249664
|
Tg(AMH-Fshr*D580H)#Hht/0
(involves: FVB/N)
|
increased cell proliferation
|
J:160015
|
increased granulosa cell proliferation
|
J:160015
|
Tg(Amh-Smad4)1Tkw/0
(involves: CD-1)
|
azoospermia
|
J:79698
|
decreased male germ cell number
|
J:79698
|
increased male germ cell apoptosis
|
J:79698
|
Tg(aP2-SREBF1c)9884Reh/0
(involves: C57BL/6J * SJL)
|
abnormal aerobic respiration
|
J:249664
|
abnormal cellular respiration
|
J:249664
|
abnormal lipid oxidation
|
J:249664
|
oxidative stress
|
J:249664
|
Tg(APCS-Ifng)5Imeg/0
(involves: C57BL/6 * DBA/2)
|
cardiac interstitial fibrosis
|
J:135124
|
Tg(APOA1)1Rub/0 Tg(APOA2)3Rub/0
(involves: C57BL/6)
|
increased cholesterol efflux
|
J:129136
|
Tg(APOA1)1Rub/Tg(APOA1)1Rub
(C57BL/6-Tg(APOA1)1Rub/J)
|
increased cholesterol efflux
|
J:107390
|
Tg(APOC1)1Lmh/Tg(APOC1)1Lmh
(involves: C57BL/6)
|
increased mast cell degranulation
|
J:135501
|
Tg(APOE-ABCA1)30Ssf/?
(C57BL/6N-Tg(APOE-ABCA1)30Ssf)
|
increased cholesterol efflux
|
J:70494
|
Tg(APOE-rtTA*M2,tetO-Rgs16)#Tmw/0
(involves: C57BL/6 * DBA)
|
decreased fatty acid oxidation
|
J:172091
|
Tg(APP-App*R609D*K612E)7Vln/0
(involves: FVB)
|
increased neuron apoptosis
|
J:32213
|
Tg(ASL1/Cryaa-Ralbp1)24Yca/0
(involves: C3H * C57BL/6 * C57BL/6J)
|
abnormal actin cytoskeleton morphology
|
J:210388
|
Tg(ATN1*)Drm21Stsu/0
(involves: 129S/SvEv * C57BL/6J)
|
abnormal cell physiology
|
J:52439
|
Tg(Atoh1-ptxA,-mCherry)1Cayo/?
(Not Specified)
|
abnormal outer hair cell kinocilium location or orientation
|
J:214064
|
Tg(AZIP/F)1Vsn/0
(FVB-Tg(AZIP/F)1Vsn/J)
|
increased pancreatic beta cell proliferation
|
J:145998
|
Tg(B4galt1-Aurkb*K111R*L323I)1Saco/0
(involves: 129/Sv * C57BL/6J * SJL)
|
abnormal male meiosis
|
J:142947
|
abnormal spermatid morphology
|
J:142947
|
decreased elongated spermatid number
|
J:142947
|
decreased round spermatid number
|
J:142947
|
oligozoospermia
|
J:142947
|
Tg(BCL2)1Tsk/0
(involves: FVB/N)
|
abnormal keratinocyte apoptosis
|
J:64948
|
Tg(BCL2)36Wehi/?
(B6.Cg-Tg(BCL2)36Wehi/J)
|
abnormal B cell proliferation
|
J:90963
|
decreased B cell apoptosis
|
J:90963
|
Tg(BCL2/IGH)1Tjd/?
(involves: C3H/He * C57BL/6)
|
abnormal mononuclear cell differentiation
|
J:81147
|
Tg(BCL2/IGH)#Jcre/0 Tg(H2-K/Igh-Traf2*)#Ywc/0
(involves: BALB/c * C57BL/6 * CBA/J * FVB/N * SJL/J * SWR/J)
|
decreased B cell apoptosis
|
J:94116
|
Tg(BCL2/IGH)M23Tjd/?
(involves: C3H/He * C57BL/6)
|
abnormal mononuclear cell differentiation
|
J:81147
|
Tg(BCL2L1)2Cbt/0
(Not Specified)
|
increased keratinocyte proliferation
|
J:65162
|
Tg(BCL2OVARY)1Ah/0
(involves: FVB)
|
abnormal spermatid morphology
|
J:134106
|
decreased granulosa cell apoptosis
|
J:55158
|
decreased male germ cell number
|
J:134106
|
increased male germ cell apoptosis
|
J:134106
|
Tg(BLG-STAT5A)15Itb/0
(involves: FVB/N)
|
increased mammary gland epithelial cell proliferation
|
J:80588
|
Tg(C9orf72_i3)112Lutzy/0
(C57BL/6J-Tg(C9orf72_i3)112Lutzy/J)
|
abnormal cell physiology
|
J:228731
|
Tg(CAG-APPL1)#Ymli/0
(involves: C57BL/6 * CBA)
|
increased skeletal muscle cell glucose uptake
|
J:230004
|
Tg(CAG-Bgeo/ALPP)1Lbe/0 Tg(CAG-en/Hoxb5,-EGFP)#Vchl/0 Tg(Hoxb3-cre)1Pkht/0
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal enteric neural crest cell migration
|
J:136122
|
Tg(CAG-Calr)#Mlk/0 Tg(Myh6-cre/Esr1*)1Liao/0
(involves: C57BL/6)
|
cardiac interstitial fibrosis
|
J:253065
|
Tg(CAG-COX7A2L)#Sinos/0
(involves: C57BL/6)
|
increased fibroblast proliferation
|
J:215964
|
Tg(CAG-cre/Esr1*)5Amc/0
(involves: C57BL/6 * CBA)
|
increased apoptosis
|
J:163367
|
Tg(CAG-cre/Esr1*)5Amc/0 Tgfbr2tm1.2Hlm/Tgfbr2tm1.2Hlm
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
increased retina apoptosis
|
J:221181
|
Tg(CAG-cre/Esr1*)5Amc/0 Wee1tm1Cxd/Wee1tm1Cxd
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
abnormal cell cycle checkpoint function
|
J:228492
|
abnormal cell morphology
|
J:228492
|
increased apoptosis
|
J:228492
|
Tg(CAG-DT)3Osb/0 Tg(Prm1-cre)1Osb/0
(involves: C57BL * DBA)
|
azoospermia
|
J:91302
|
Tg(CAG-EGFP)50Osb/0
(involves: C3H/HeSlc * C57BL/6Slc)
|
cellular phenotype
|
J:174672
|
Tg(CAG-EGFP)D4Nagy/0 Xisttm5.2Nbd/Xist+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:171502
|
Tg(CAG-EGFP,RNU6-RNAi:Sly)367Psb/0
(involves: C57BL/10 * CBA/Ca * MF1 * RIII)
|
abnormal sperm head morphology
|
J:155571
|
abnormal sperm motility
|
J:155571
|
oligozoospermia
|
J:155571
|
Tg(CAG-EGFP/Map1lc3b)53Nmz/0 Tg(Myh6-Gsk3b*)19Jusa/0
(involves: C57BL/6NCrj * FVB/N)
|
abnormal autophagy
|
J:186597
|
Tg(CAG-en/Hoxb5,-EGFP)#Vchl/0 Tg(Hoxb3-cre)1Pkht/0
(Not Specified)
|
abnormal enteric neural crest cell migration
|
J:136122
|
Tg(CAG-Has2)99Nita/0 Tg(MMTV-cre)4Mam/0 Tg(MMTVneu)202Mul/0
(FVB.Cg-Tg(CAG-Has2)99Nita Tg(MMTV-cre)4Mam Tg(MMTVneu)202Mul)
|
impaired macrophage chemotaxis
|
J:164205
|
Tg(CAG-Lyn*)#Paau/0
(B6.Cg-Tg(CAG-Lyn*)#Paau)
|
increased keratinocyte proliferation
|
J:151886
|
Tg(CAG-Naa10)10Jprk/0
(involves: C57BL/6)
|
abnormal osteoblast physiology
|
J:276208
|
impaired osteoblast differentiation
|
J:276208
|
Tg(CAG-Naa10)15Jprk/0
(involves: C57BL/6)
|
abnormal osteoblast physiology
|
J:276208
|
impaired osteoblast differentiation
|
J:276208
|
Tg(CAG-Ndufab1)#Xiwa/0
(involves: C57BL/6J)
|
abnormal redox activity
|
J:293657
|
cellular phenotype
|
J:293657
|
Tg(CAG-NRIP1)51Row/0
(involves: FVB/N)
|
abnormal myocardial fiber mitochondrial morphology
|
J:175885
|
abnormal respiratory electron transport chain
|
J:175885
|
cardiac interstitial fibrosis
|
J:175885
|
decreased mitochondrial number
|
J:175885
|
Tg(CAG-OVAL)916Jen/?
(C57BL/6-Tg(CAG-OVAL)916Jen)
|
abnormal cell morphology
|
J:91742
|
Tg(CAG-p35)1Miur/0 Tg(Mbp-cre)29Miur/0
(involves: C57BL/6)
|
decreased apoptosis
|
J:126593
|
Tg(CAG-PLA2G3)#aMurm/0
(Not Specified)
|
increased mast cell degranulation
|
J:197334
|
Tg(CAG-Ppard*E411P)#Als/0 Tg(Nes-cre)1Kln/0
(B6J.Cg-Tg(Nes-cre)1Kln Tg(CAG-Ppard*E411P)#Als)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:233176
|
decreased mitochondrial size
|
J:233176
|
Tg(CAG-SAC/EGFP)35Rang/0 Tg(TRAMP)8247Ng/0
(involves: C3H * C57BL/6)
|
increased apoptosis
|
J:125633
|
Tg(CAG-SNCA*)1.1Ccs/?
(involves: C57BL/6)
|
abnormal mitochondrial morphology
|
J:127707,
J:168847
|
abnormal mitochondrial physiology
|
J:168847
|
Tg(CAG-SPTLC1*C133W)8EAmcc/0
(involves: C3H * C57BL/6)
|
asthenozoospermia
|
J:155748
|
oligozoospermia
|
J:155748
|
Tg(CAG-SYVN1)1Tn/?
(D1.Cg-Tg(CAG-SYVN1)1Tn)
|
decreased apoptosis
|
J:86009
|
Tg(CAG-Tmem135)#Aike/0
(involves: C57BL/6J * FVB/NJ)
|
abnormal mitochondrial morphology
|
J:237184
|
abnormal mitochondrial physiology
|
J:237184
|
decreased mitochondrial size
|
J:237184
|
increased mitochondrial fission
|
J:237184
|
oxidative stress
|
J:237184
|
Tg(CAG-Ubqln1)2Hmw/0
(involves: C57BL/6 * SJL)
|
decreased cellular sensitivity to oxidative stress
|
J:206930
|
decreased hepatocyte apoptosis
|
J:206930
|
Tg(CAG-WRN*K577M)5025Wcl/0
(involves: C3H * C57BL/6J)
|
abnormal cell physiology
|
J:95127
|
Tg(Camk2a-App*,-Apbb1)25Spim/0
(C57BL/6-Tg(Camk2a-App*,-Apbb1)25Spim)
|
increased susceptibility to neuronal excitotoxicity
|
J:153738
|
Tg(Camk2a-Bdnf)A9Stl/0
(involves: C57BL/6 * DBA/2)
|
abnormal neuron differentiation
|
J:57645
|
Tg(CAMK2A-CAST)7Tcs/0
(involves: C57BL/6Cr)
|
decreased susceptibility to neuronal excitotoxicity
|
J:109976,
J:98730
|
Tg(Camk2a-Gpr85)1Mima/?
(involves: C57BL/6 * DBA)
|
increased neuron apoptosis
|
J:134303
|
Tg(Camk2a-MAPT)601Ymot/0
(involves: C57BL/6 * C57BL/6J)
|
decreased cellular glucose uptake
|
J:172762
|
Tg(Camk2a-Polg*D181A)BTkato/0
(C57BL/6J-Tg(Camk2a-Polg*D181A)BTkato)
|
abnormal mitochondrial chromosome morphology
|
J:127895
|
Tg(Camk2a-Tardbp)#Ckjs/Tg(Camk2a-Tardbp)#Ckjs
(FVB/N-Tg(Camk2a-Tardbp)#Ckjs)
|
increased neuron apoptosis
|
J:163612
|
Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-LRRK2*G2019S)E3Cai/0 Tg(tetO-SNCA*A53T)E2Cai/0
(involves: C57BL/6)
|
abnormal neuron mitochondrial morphology
|
J:156512
|
Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-SNCA)0Olri/0
(involves: C57BL/6)
|
abnormal neuron differentiation
|
J:132774
|
Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-SNCA*A53T)33Vle/0
(involves: C3H/HeH * C57BL/6)
|
increased neuron apoptosis
|
J:156801
|
Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-SNCA*A53T)E2Cai/0
(involves: C57BL/6)
|
abnormal neuron mitochondrial morphology
|
J:156512
|
Tg(CD2-Ccdc86)1Hfuj/?
(B6.FVB-Tg(CD2-Ccdc86)1Hfuj)
|
increased T cell apoptosis
|
J:151722
|
Tg(CD2-Ceacam1*4L)1Rsb/0
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:116136
|
Tg(CD2-Fos)#Liux/0
(Not Specified)
|
decreased apoptosis
|
J:190150
|
Tg(CD2-Lrch1)#Liux/0
(involves: C57BL/6)
|
abnormal cellular extravasation
|
J:238772
|
Tg(CD2-Myb/en)2Kmw/?
(involves: C57BL/10 * CBA)
|
decreased T cell proliferation
|
J:126456
|
Tg(CD2-Myb/en)2Kmw/Tg(CD2-Myb/en)2Kmw
(involves: C57BL/10 * CBA)
|
decreased T cell proliferation
|
J:126456
|
Tg(CD2-Nfat5)1Snh/0
(involves: BALB/c * C57BL/6)
|
decreased splenocyte proliferation
|
J:80066
|
decreased T cell proliferation
|
J:80066
|
Tg(CD2-S1PR1)1Ejg/?
(involves: C57BL/6 * DBA/2)
|
abnormal lymphocyte chemotaxis
|
J:96558
|
decreased T cell proliferation
|
J:96558
|
impaired leukocyte migration
|
J:96558
|
Tg(CD2-TcraF5,CD2-TcrbF5)1Kio/0 Tg(Cd4-BCL2*G101A*D102A*D103A)AWnt/0
(involves: C57BL/6 * C57BL/10)
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(CD2-TcraF5,CD2-TcrbF5)1Kio/0 Tg(LCKprBCL2)36Sjk/0
(involves: C57BL/6 * C57BL/10)
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(CD2-Tgfbr2)1Grs/0
(C57BL/6-Tg(CD2-Tgfbr2)1Grs/Nci)
|
increased T cell proliferation
|
J:97523
|
Tg(CD2-Tgfbr2)1Grs/?
(C57BL/6-Tg(CD2-Tgfbr2)1Grs/Nci)
|
increased T cell proliferation
|
J:93665
|
Tg(Cd3d-Il5)NJ.1638Nal/?
(involves: C57BL/6J * CBA/J)
|
abnormal eosinophil differentiation
|
J:123440
|
Tg(Cd4-BCL2*G101A*D102A*D103A)AWnt/0
(involves: C57BL/6)
|
abnormal T cell proliferation
|
J:217939
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(Cd4-BCL2*G101A*D102A*D103A)AWnt/0
(involves: C57BL/6 * CBA/J)
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(Cd4-BCL2*G101A*D102A*D103A)AWnt/0 Tg(Nr4a1-EGFP/cre)820Khog/0
(involves: C57BL/6 * C57BL/6J)
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(Cd4-BCL2*G101A*D102A*D103A)AWnt/0 Tg(TcraH-Y,TcrbH-Y)71Vbo/0
(involves: C57BL/6 * C57BL/6J * DBA/2J)
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(Cd4-cre)1Cwi/0 Trmt6em1Hbgl/Trmt6em1Hbgl
(involves: C57BL/6 * DBA/2J)
|
decreased T cell proliferation
|
J:336736
|
Tg(Cd4-cre)1Cwi/0 Trmt61aem1Hbgl/Trmt61aem1Hbgl
(involves: C57BL/6 * DBA/2J)
|
decreased T cell proliferation
|
J:336736
|
Tg(Cd4-Dtx1)1Mzl/?
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:151605
|
Tg(Cd4-TGFBR2)16Flv/?
(involves: C3H * C57BL/6 * C57BL/10 * C57BR/cd)
|
abnormal T cell proliferation
|
J:97554
|
Tg(Cd4-TGFBR2)16Flv/?
(involves: C3H * C57BL/6)
|
abnormal T cell proliferation
|
J:134473
|
Tg(CD19)1Tft/0
(involves: C57BL/6 * C57BL/6J * SJL)
|
increased B cell proliferation
|
J:27236
|
Tg(CD19)1Tft/Tg(CD19)1Tft
(involves: C57BL/6 * C57BL/6J * SJL)
|
increased B cell proliferation
|
J:27236
|
Tg(CD46)2Gsv/0
(involves: C57BL/6 * FVB/N)
|
increased neuron apoptosis
|
J:109895
|
Tg(Cd68-BCL2)526Medz/0
(involves: 129 * C57BL/6)
|
decreased apoptosis
|
J:82809
|
Tg(Cd68-BCL2)535Medz/0
(involves: 129 * C57BL/6)
|
decreased dendritic cell apoptosis
|
J:211458
|
Tg(Cd79b-TCL1A)BKTeit/0
(involves: C3H * C57BL/6)
|
decreased B cell apoptosis
|
J:79703
|
decreased T cell apoptosis
|
J:79703
|
increased B cell proliferation
|
J:79703
|
increased T cell proliferation
|
J:79703
|
Tg(Cga-LHB/CGB)94Jhn/?
(involves: C57BL/6 * SJL)
|
impaired luteal cell differentiation
|
J:55157
|
Tg(Ckm-IGF1R*K1003R)1Dlr/0
(FVB/N-Tg(Ckm-IGF1R*K1003R)1Dlr)
|
decreased cellular glucose uptake
|
J:71205
|
decreased muscle cell glucose uptake
|
J:71205
|
Tg(Ckm-Ppara)HEDpk/0
(involves: C57BL/6 * CBA)
|
decreased muscle cell glucose uptake
|
J:129848
|
Tg(Ckm-Ppard)MEDpk/0
(involves: C57BL/6 * CBA)
|
abnormal muscle cell glucose uptake
|
J:129848
|
Tg(Ckm-Ppargc1a)31Brsp/0
(C57BL/6-Tg(Ckm-Ppargc1a)31Brsp/J)
|
abnormal aerobic respiration
|
J:176080
|
increased mitochondrial fission
|
J:176080
|
Tg(Ckm-Ppargc1b)T37Brsp/0
(FVB-Tg(Ckm-Ppargc1b)T37Brsp)
|
abnormal mitochondrial morphology
|
J:118258
|
Tg(Ckm-PTPN1)45Bbk/0
(involves: FVB)
|
decreased skeletal muscle cell glucose uptake
|
J:122895
|
Tg(Ckm-PTPN1)45Bbk/? Tg(Ckm-PTPRF)13Bbk/?
(involves: FVB)
|
decreased skeletal muscle cell glucose uptake
|
J:122895
|
Tg(Ckm-PTPRF)13Bbk/0
(involves: FVB)
|
decreased skeletal muscle cell glucose uptake
|
J:122895
|
Tg(Ckmm-Ucp1)1Boud/0
(involves: C57BL/6J * DBA/2J)
|
abnormal cellular respiration
|
J:80053
|
Tg(Ckmm-Ucp1)1Boud/Tg(Ckmm-Ucp1)1Boud
(involves: C57BL/6J * DBA/2J)
|
abnormal cellular respiration
|
J:80053
|
Tg(CMV-APPL2)1Smoc/0
(Not Specified)
|
decreased skeletal muscle cell glucose uptake
|
J:230004
|
Tg(CMV-ATXN3*94Q)94Pama/0
(B6.FVB-Tg(CMV-ATXN3*94Q)94Pama)
|
abnormal cell physiology
|
J:163032
|
Tg(CMV-cat,-ROCK2*)3-1Koba/0 Tg(Tagln-cre)1Her/0
(involves: C57BL/6 * C57BL/6JJcl * DBA/2 * SJL)
|
abnormal fetal cardiomyocyte proliferation
|
J:242116
|
Tg(CMV-cre)1Cgn/0 Trp53tm4Att/Trp53+
(involves: 129S4/SvJae * BALB/cJ * C57BL/6J)
|
decreased cell proliferation
|
J:217080
|
increased apoptosis
|
J:217080
|
Tg(CMV-Gja1)BClo/0
(involves: CD-1 * SJL/J * SWR/J)
|
abnormal cell physiology
|
J:40388
|
Tg(CMV-IghvaD11)CCat/0 Tg(CMV-IgkvaD11)BCat/0
(involves: C57BL/6 * SJL)
|
increased neuron apoptosis
|
J:79946
|
increased splenocyte apoptosis
|
J:79946
|
Tg(CMV-IghvaD11)DCat/0 Tg(CMV-IgkvaD11)ACat/0
(involves: C57BL/6 * SJL)
|
increased neuron apoptosis
|
J:79946
|
increased splenocyte apoptosis
|
J:79946
|
Tg(CMV-MYOC*Y437H)#Vcs/0
(involves: C57BL/6J * SJL/J)
|
abnormal endoplasmic reticulum morphology
|
J:178254
|
increased endoplasmic reticulum stress
|
J:178254
|
Tg(CMV-SALL4_iB)#Chai/?
(Not Specified)
|
binucleate
|
J:115037
|
increased apoptosis
|
J:115037
|
Tg(CMV-tTA)3Bjd/0 Tg(tetO-Prkar1a*x2as)1Stra/0
(involves: C57BL/6 * NMRI * SJL)
|
retention of the adrenal gland x-zone
|
J:95465
|
Tg(CNTN2-CNTN1)1Gnn/0
(involves: C57BL/10 * CBA)
|
abnormal Purkinje cell differentiation
|
J:80098
|
Tg(Col1a1-Atf4)1Kry/0
(involves: FVB)
|
decreased pancreatic beta cell proliferation
|
J:152695
|
Tg(Col1a1-cre)1Kry/0 Vdrtm2Ska/Vdrtm2Ska
(involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj * FVB/N)
|
abnormal osteoclast differentiation
|
J:196471
|
Tg(Col1a1-Cthrc1)1Haak/0
(B6.Cg-Tg(Col1a1-Cthrc1)1Haak)
|
abnormal osteoblast physiology
|
J:143940
|
increased osteoblast proliferation
|
J:143940
|
Tg(Col1a1-Dkk1)1Hmk/?
(B6.FVB-Tg(Col1a1-Dkk1)1Hmk)
|
abnormal cell cycle
|
J:238121
|
impaired osteoblast differentiation
|
J:158620
|
Tg(Col1a1-Mir34c)#Kry/0
(B6.Cg-Tg(Col1a1-Mir34c)#Kry)
|
abnormal osteoblast physiology
|
J:185130
|
decreased osteoblast proliferation
|
J:185130
|
Tg(Col1a1-Ptprv)1Kry/?
(Not Specified)
|
decreased pancreatic beta cell proliferation
|
J:126780
|
Tg(Col1a1-Runx2)#Pmt/0
(involves: BALB/c * C57BL/6)
|
abnormal osteoblast differentiation
|
J:167992
|
Tg(COL2A1*R519C)#Afe/0
(involves: FVB/N)
|
abnormal Golgi cisterna morphology
|
J:307985
|
Tg(COL2A1*R519C)#Afe/Tg(COL2A1*R519C)#Afe
(involves: FVB/N)
|
abnormal Golgi cisterna morphology
|
J:307985
|
Tg(Col2a1-cre/ERT2)1Dic/0 Tgfbr1tm1.1Karl/Tgfbr1tm1.1Karl
(involves: 129 * C57BL/6)
|
increased chondrocyte apoptosis
|
J:271724
|
Tg(Col2a1-Fgfr3/GH)BDor/0
(FVB/N-Tg(Col2a1-Fgfr3/GH)BDor)
|
abnormal osteoclast differentiation
|
J:50292
|
Tg(Col2a1-rtTA,tetO-COMP*)2Jath/0
(C57BL/6-Tg(Col2a1-rtTA,tetO-COMP*)2Jath)
|
increased chondrocyte apoptosis
|
J:233238
|
Tg(Col10a1-Tg*L2263P)1Rpbh/0
(Not Specified)
|
increased endoplasmic reticulum stress
|
J:154052
|
Tg(Col10a1-Tg*L2263P)1Rpbh/Tg(Col10a1-Tg*L2263P)1Rpbh
(Not Specified)
|
increased endoplasmic reticulum stress
|
J:154052
|
Tg(Cr2-cre)3Cgn/? Xrcc4tm1Fwa/Xrcc4tm2Fwa
(involves: 129P2/OlaHsd * 129S6/SvEvTac)
|
spontaneous chromosome breakage
|
J:150339
|
Tg(Cryaa-TAg,Ins2-CALM1)26Ove/0
(FVB-Tg(Cryaa-TAg,Ins2-CALM1)26Ove)
|
abnormal aerobic respiration
|
J:106851
|
increased mitochondrial size
|
J:106851
|
Tg(Cryaa-TAg,Ins2-CALM1)26Ove/0 Tg(Myh6-SOD2,Tyr)3Pne/0
(FVB-Tg(Cryaa-TAg,Ins2-CALM1)26Ove Tg(Myh6-SOD2,Tyr)3Pne)
|
cellular phenotype
|
J:106815
|
Tg(Csf1r-Tnfsf15,-EGFP)#Targ/0
(involves: C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:169462
|
Tg(CTSG-RARA/ZBTB16)#Ppp/0
(Not Specified)
|
decreased apoptosis
|
J:65878
|
Tg(CTSG-RARA/ZBTB16)#Ppp/0 Tg(CTSG-ZBTB16/RARA)#Ppp/0
(Not Specified)
|
decreased apoptosis
|
J:65878
|
Tg(CYP1A1-PPARD)#Jfoe/0
(involves: C57BL/6J * CBA)
|
increased keratinocyte proliferation
|
J:158907
|
increased T cell proliferation
|
J:158907
|
Tg(Cyp17a1-NGF)2456Oje/Tg(Cyp17a1-NGF)2456Oje
(involves: C57BL/6J * DBA/2J)
|
increased granulosa cell apoptosis
|
J:158186
|
Tg(Dct-Birc5)21Gros/0
(involves: C57BL/6 * CBA)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:122181
|
Tg(Dct-Birc5)21Gros/0 Tg(Mt1-Hgf)19Lmb/0
(involves: C57BL/6 * CBA * FVB/N)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:122181
|
Tg(Dct-Grm1)ESzc/0
(involves: C57BL/6J)
|
abnormal melanocyte proliferation
|
J:83183
|
Tg(Dct-Grm1)ESzc/0
(C57BL/6J-Tg(Dct-Grm1)ESzc)
|
abnormal melanocyte proliferation
|
J:230115
|
Tg(Dct-Hes1)#Nshk/0
(Not Specified)
|
decreased melanoblast apoptosis
|
J:111228
|
Tg(Dct-lacZ)A12Jkn/0 Tg(Tyr-Ctnnb1/EGFP)#Lru/0
(B6.Cg-Tg(Tyr-Ctnnb1/EGFP)#Lru Tg(Dct-lacZ)A12Jkn)
|
decreased melanoblast proliferation
|
J:176245
|
Tg(Ddx4-cre)1Dcas/0 Uxttm1.1Sklo/Y
(involves: 129S1/Sv * C57BL/6 * FVB)
|
arrest of male meiosis
|
J:261955
|
azoospermia
|
J:261955
|
increased male germ cell apoptosis
|
J:261955
|
Tg(Disc1/EGFP)M19Sshe/0
(involves: C57BL/6JCrl * CBA/CaCrl)
|
abnormal axon extension
|
J:143557
|
abnormal neuron proliferation
|
J:143557
|
Tg(DM15)26Bew/0
(involves: FVB)
|
abnormal skeletal muscle fiber mitochondrial morphology
|
J:93614
|
cardiac interstitial fibrosis
|
J:93614
|
Tg(DMWD,DMPK*,SIX5)1177Ggo/0
(involves: C57BL/6 * DBA/2)
|
increased mitochondrial number
|
J:73187
|
increased mitochondrial size
|
J:73187
|
Tg(DYRK1A)36Wjs/0
(involves: C57BL/6NCrjBgi)
|
abnormal neuron proliferation
|
J:166796
|
abnormal neuronal precursor proliferation
|
J:166796
|
Tg(Dyrk1a)189N3Yah/0
(B6.129P2-Tg(Dyrk1a)189N3Yah/Yah)
|
abnormal spermatogonia morphology
|
J:324151
|
oligozoospermia
|
J:324151
|
Tg(EEF1A1-SHC1*)1Ravi/0 Tg(Nes-cre)1Kln/0
(involves: 129 * C57BL/6 * SJL)
|
increased neuron apoptosis
|
J:111058
|
Tg(EIF1AX-Aldh2*E487K)101Oht/Tg(EIF1AX-Aldh2*E487K)101Oht
(C57BL/6-Tg(EIF1AX-Aldh2*E487K)101Oht)
|
increased sensitivity to induced cell death
|
J:137374
|
oxidative stress
|
J:137374
|
Tg(EIF1AX-PMS2*)685Tcar/0
(involves: C57BL/6 * SJL)
|
abnormal cell physiology
|
J:152364
|
abnormal mismatch repair
|
J:152364
|
Tg(EIF1AX-PMS2*)685Tcar/0 Tg(TacLIZa)A1Jsh/0
(involves: C57BL/6 * SJL)
|
abnormal cell physiology
|
J:152364
|
abnormal DNA repair
|
J:152364
|
Tg(EIIa-cre)C5379Lmgd/0 Tg(Rnu6-RNAi:Bccip)4Zshn/0
(involves: C57BL/6 * FVB/N)
|
decreased cell proliferation
|
J:176115
|
decreased inner cell mass proliferation
|
J:176115
|
increased embryonic tissue cell apoptosis
|
J:176115
|
Tg(EIIa-cre)C5379Lmgd/? Trip11tm1.2Psmi/Trip11tm1.2Psmi
(involves: 129/Sv * C57BL/6 * FVB/N)
|
abnormal endoplasmic reticulum morphology
|
J:253969
|
Tg(Emu-TXLNA)1Amjr/0
(B6.Cg-Tg(Emu-TXLNA)1Amjr)
|
abnormal mesangial cell morphology
|
J:117018
|
Tg(EmuSR-HDAC9)1468Kpet/0
(involves: C57BL/6 * CBA)
|
increased B cell proliferation
|
J:237420
|
Tg(Eno2-APPSwe)1223-3Ykk/0
(involves: C57BL/6 * DBA/2)
|
increased neuron apoptosis
|
J:100955
|
Tg(Eno2-Bmp4)3Jake/0
(involves: BALB/c * C57BL/6)
|
abnormal radial glial cell morphology
|
J:82446
|
Tg(Eno2-MFN2*R94Q)L51Ugfm/0
(involves: C57BL/6 * DBA/2)
|
increased mitochondrial number
|
J:173431
|
Tg(Eno2-MFN2*R94Q)L87Ugfm/Tg(Eno2-MFN2*R94Q)L87Ugfm
(involves: C57BL/6 * DBA/2)
|
increased mitochondrial number
|
J:173431
|
Tg(Eno2-PSEN1)1Gae/0
(involves: C57BL/6J * DBA/2J)
|
abnormal neuron differentiation
|
J:100959
|
Tg(Eno2-PSEN1*P117L)1Gae/0
(involves: C57BL/6J * DBA/2J)
|
abnormal neuron differentiation
|
J:100959
|
Tg(Eno2-PTGS2)32Pasi/0
(involves: C3H/HeNTac * C57BL/6NTac)
|
increased susceptibility to neuronal excitotoxicity
|
J:100973
|
Tg(Erbb2)1Jek/0
(involves: C57BL/6 * SJL)
|
abnormal keratinocyte differentiation
|
J:47225
|
Tg(Fabp1-Ccnd1)4Rdb/0
(C57BL/6-Tg(Fabp1-Ccnd1)4Rdb/J)
|
increased hepatocyte apoptosis
|
J:70394
|
Tg(Fabp4-Angptl2)5Yo/0
(involves: C57BL/6)
|
abnormal macrophage chemotaxis
|
J:152387
|
Tg(Fabp4-LMNA*R482Q)11ACdl/0
(FVB-Tg(Fabp4-LMNA*R482Q)11ACdl)
|
decreased adipocyte glucose uptake
|
J:149858
|
decreased muscle cell glucose uptake
|
J:149858
|
Tg(Fabp4-LMNA*R482Q)17CCdl/0
(FVB/N-Tg(Fabp4-LMNA*R482Q)17CCdl)
|
abnormal muscle cell glucose uptake
|
J:149858
|
Tg(Fsip2)#Nali/0
(C57BL/6-Tg(Fsip2)#Nali)
|
abnormal sperm midpiece morphology
|
J:307606
|
abnormal sperm principal piece morphology
|
J:307606
|
elongated sperm flagellum
|
J:307606
|
Tg(FXN)YG8Pook/0
(B6.Cg-Tg(FXN)YG8Pook)
|
abnormal chromosome morphology
|
J:91581
|
cellular phenotype
|
J:91581
|
Tg(FXN)YG22Pook/0
(B6J.Cg-Tg(FXN)YG22Pook)
|
abnormal cell physiology
|
J:91581
|
abnormal chromosome morphology
|
J:91581
|
Tg(GFAP)10Mes/0 Tg(GFAP-CRYAB)141.6Mes/0
(involves: FVB/N)
|
abnormal cell physiology
|
J:146191
|
Tg(Gfap-gp120)#Lms/0
(involves: C57BL/6 * SJL)
|
decreased neuronal precursor proliferation
|
J:170738
|
Tg(GFAP-Hras1)2Agu/Tg(GFAP-Hras1)2Agu
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
trisomy
|
J:69129
|
Tg(Gfap-TK)7.1Mvs/0
(involves: C57BL/10 * CBA * CFLP)
|
abnormal cell death
|
J:104241
|
abnormal cell proliferation
|
J:113202
|
abnormal intestinal goblet cell morphology
|
J:104241
|
abnormal neuron differentiation
|
J:94543
|
gangrene
|
J:104241
|
increased susceptibility to neuronal excitotoxicity
|
J:113202
|
Tg(Gfap-TNF*)K21Gkl/0
(involves: C57BL/6 * CBA)
|
abnormal oligodendrocyte apoptosis
|
J:106592
|
Tg(GFAP-tTA)6Hyms/0 Tg(tetO-HMOX1)6Hyms/0
(involves: FVB/N)
|
abnormal autophagy
|
J:186620,
J:190573
|
abnormal mitochondrial crista morphology
|
J:186620,
J:190573
|
abnormal mitochondrial inner membrane morphology
|
J:190573
|
abnormal mitochondrial morphology
|
J:186620,
J:190573
|
disorganized mitochondrial cristae
|
J:186620
|
oxidative stress
|
J:186620,
J:190573
|
Tg(GNB1L,TBX1,GP1BB,SEPT5)23Bem/0
(either: FVB-Tg(GNB1L,TBX1,GP1BB,SEPT5)23Bem or (involves: C57BL/6 * FVB))
|
patent ductus arteriosus
|
J:67796
|
Tg(H2-Ea-G6pc2)69Tkay/?
(NOD-Tg(H2-Ea-G6pc2)69Tkay)
|
decreased T cell proliferation
|
J:117352
|
Tg(H2-Ea-Ins2)1Wehi/0
(NOD/ShiLtJWehi-Tg(H2-Ea-Ins2)1Wehi)
|
abnormal T cell proliferation
|
J:100232
|
Tg(H2-Ea-Ins2)1Wehi/Tg(H2-Ea-Ins2)1Wehi
(NOD/ShiLtJWehi-Tg(H2-Ea-Ins2)1Wehi)
|
decreased T cell proliferation
|
J:117352
|
Tg(H2-K1-Ifnb1)10Seif/Tg(H2-K1-Ifnb1)10Seif
(C3H/HeOuJ-Tg(H2-K1-Ifnb1)10Seif)
|
abnormal male germ cell apoptosis
|
J:174828
|
oligozoospermia
|
J:174828
|
Tg(H2-K-BCL2)1Josd/0
(involves: C57BL/6 * C57BL/Ka * C3H)
|
decreased cellular sensitivity to X-ray irradiation
|
J:80894
|
Tg(H2-K-DUSP5)21Wjl/0
(involves: C57BL/6J * CBA)
|
decreased T cell proliferation
|
J:138077
|
Tg(H2-K-Fosl1)1Wag/0
(involves: C57BL/6 * CBA)
|
abnormal osteoblast physiology
|
J:64494
|
enhanced osteoblast differentiation
|
J:64494
|
Tg(H2-K-HLA-G,B2M)1Alm/0
(CBA/Ca-Tg(H2-K-HLA-G,B2M)1Alm/CmwJ)
|
increased T cell proliferation
|
J:140016
|
Tg(H2-K-MC159/EGFP)13Fkmc/0
(involves: C57BL/6)
|
decreased B cell apoptosis
|
J:138050
|
decreased sensitivity to induced cell death
|
J:138050
|
decreased T cell apoptosis
|
J:138050
|
increased B cell proliferation
|
J:138050
|
Tg(H2-Kb-IL21)5Wjl/0
(involves: 129)
|
increased B cell apoptosis
|
J:93740
|
Tg(H2KmPCC)2939Stoe/0 Tg(Tcra2B4)1Mmd/0 Tg(Tcrb2B4)1Mmd/0
(involves: C3H/HeJ * C57BL/6 * SJL)
|
decreased T cell proliferation
|
J:50143
|
Tg(HBA1-GFP)1Ew/Tg(HBA1-GFP)1Ew WizMommeD30/Wiz+
(involves: C57BL/6J * FVB/N)
|
abnormal epigenetic regulation of gene expression
|
J:201508
|
Tg(HBV-HCV)21Kko/0
(C57BL/6N-Tg(HBV-HCV)21Kko)
|
abnormal mitochondrial inner membrane morphology
|
J:52686
|
Tg(HBV-HCV)49Kko/0
(C57BL/6N-Tg(HBV-HCV)49Kko)
|
abnormal mitochondrial inner membrane morphology
|
J:52686
|
Tg(HBV-HCV)Kko/0
(C57BL/6N-Tg(HBV-HCV)Kko)
|
abnormal mitochondrial inner membrane morphology
|
J:69727,
J:52686
|
oxidative stress
|
J:69727
|
Tg(HBVX*,-Myc)#Skp/Tg(HBVX*,-Myc)#Skp
(Not Specified)
|
abnormal cell nucleus morphology
|
J:202732
|
abnormal hepatocyte mitochondrial morphology
|
J:202732
|
Tg(HBx-HCV)C5Tto/0
(involves: C57BL/6 * DBA/2)
|
abnormal mitochondrial shape
|
J:105313
|
Tg(HDexon1)61Gpb/0
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal cell physiology
|
J:188338
|
Tg(HIV)26Aln/0
(involves: FVB/N)
|
increased lens epithelium apoptosis
|
J:136652
|
increased lens fiber apoptosis
|
J:136652
|
Tg(Hoxc13)61B1Awg/0
(FVB-Tg(Hoxc13)61B1Awg)
|
increased keratinocyte proliferation
|
J:68213
|
Tg(Hoxc13)61U4Awg/0
(FVB-Tg(Hoxc13)61U4Awg)
|
increased keratinocyte proliferation
|
J:68213
|
Tg(Igh*-Mir125b-1)116Toki/0
(Not Specified)
|
decreased B cell apoptosis
|
J:178816
|
Tg(Igh-Lmp2a)13FRdni/0
(involves: C57BL/6 * CD-1 * SJL)
|
maternal imprinting
|
J:56614
|
Tg(Igh-Lmp2a)ERlon/0
(involves: C57BL/6 * SJL)
|
abnormal B cell proliferation
|
J:129571
|
Tg(Igh-Mir29a,-Mir29b-1,-hrGFP)#Cro/0
(FVB/N-Tg(Igh-Mir29a,-Mir29b-1,-hrGFP)#Cro)
|
increased B cell proliferation
|
J:162077
|
Tg(Igh-Mir155)8Cro/0
(involves: FVB/N)
|
increased B cell proliferation
|
J:109591
|
Tg(Igh-V-CD40lg)#Tsub/0
(involves: C57BL/6)
|
abnormal colon goblet cell morphology
|
J:89855
|
increased splenocyte proliferation
|
J:89855
|
Tg(IghelMD4)4Ccg/Tg(IghelMD4)4Ccg
(NOD.B6-Tg(IghelMD4)4Ccg/DvsJ)
|
abnormal T cell proliferation
|
J:80859
|
Tg(IghMyc)22Bri/0
(involves: C57BL/6N * SJL)
|
increased B cell apoptosis
|
J:214383
|
Tg(IghMyc)22Bri/0 Xiaptm1Hs/Xiaptm1Hs
(B6.Cg-Xiaptm1Hs Tg(IghMyc)22Bri)
|
decreased B cell proliferation
|
J:138979
|
increased B cell apoptosis
|
J:138979
|
Tg(IghMyc)186Brn/0
(involves: C57BL/LiA * CBA/BrA)
|
abnormal cell cycle
|
J:142390
|
abnormal intracellular organelle morphology
|
J:142390
|
abnormal mitosis
|
J:142390
|
binucleate
|
J:142390
|
Tg(IghMyc)186Brn/0 Rpl24Bst/Rpl24+
(involves: C57BL/LiA * C57BLKS * CBA/BrA)
|
cellular phenotype
|
J:142390
|
increased apoptosis
|
J:142390
|
Tg(IghMyc)186Brn/0 Rpl38tm1Rugg/Rpl38+
(involves: C57BL/LiA * CBA/BrA)
|
cellular phenotype
|
J:142390
|
increased apoptosis
|
J:142390
|
Tg(ILK3mHEL)3Ccg/0 Tg(TcrHEL3A9)1Mmd/0
(involves: C57BL/6JSfd * C57BL/10Sg * C57BR/cd)
|
abnormal T cell proliferation
|
J:78309
|
Tg(Ins2-Cebpb)2Maka/0
(involves: C57BL/6)
|
increased pancreatic islet cell apoptosis
|
J:156725
|
Tg(Ins2-crmA)27Ngkh/?
(NOD-Tg(Ins2-CrmA)27Ngkh)
|
decreased sensitivity to induced cell death
|
J:132052
|
Tg(Ins2-HA)165Bri/0
(B10.Cg- H2d Tg(Ins2-HA)165Bri/ShrmJ)
|
decreased T cell proliferation
|
J:86430
|
Tg(Ins2-IAPP)L13Gjsc/0
(FVB/N-Tg(Ins2-IAPP)L13Gjsc)
|
increased pancreatic beta cell apoptosis
|
J:142009
|
Tg(Ins2-IAPP)RHFSoel/Tg(Ins2-IAPP)RHFSoel
(involves: FVB/N)
|
increased pancreatic beta cell apoptosis
|
J:130022
|
Tg(Ins2-Mir184)4Mnpy/0
(Not Specified)
|
decreased pancreatic beta cell proliferation
|
J:210552
|
Tg(Ins2-Mirc13)E4Biat/0
(C57BL/6N-Tg(Ins2-Mirc13)E4Biat)
|
increased pancreatic beta cell apoptosis
|
J:314874
|
Tg(Ins2-Nos2)40Okam/0 Tg(Kdr-AGER)102Hyam/0
(involves: C57BL/6J * CBA/J * CD-1 * DBA/2)
|
increased kidney cell proliferation
|
J:70495
|
Tg(Ins2-rtTA)2Efr/0 Tg(tetO-Ago2)30Mnpy/0
(involves: C57BL/6 * CBA)
|
increased pancreatic beta cell proliferation
|
J:210552
|
Tg(Ins2-rtTA)2Efr/0 Tg(tetO-DTA)1Gfi/0
(involves: C57BL/6 * CBA)
|
increased apoptosis
|
J:127412
|
Tg(Ins2-rtTA)2Efr/0 Tg(tetO-Mir184)#Mnpy/0
(involves: C57BL/6 * CBA)
|
decreased pancreatic beta cell proliferation
|
J:210552
|
Tg(Ins2-TCF1*P291)2Kya/0
(involves: C57BL/6 * SJL)
|
decreased pancreatic beta cell proliferation
|
J:73760
|
Tg(Ins2-TFRC/OVA)296Wehi/0
(involves: C57BL/6)
|
abnormal leukocyte migration
|
J:98589
|
Tg(Ins2-TFRC/OVA)296Wehi/0 1700016L21RikTg(Itgax-HBEGF/EGFP)57Lan/0
(involves: C57BL/6 * FVB)
|
decreased T cell proliferation
|
J:122114
|
Tg(Ins-MYC/Er)1Gev/0
(involves: C57BL/6 * CBA)
|
increased apoptosis
|
J:142030
|
increased cell proliferation
|
J:142030
|
Tg(IRS1)1Mhep/0
(FVB-Tg(IRS1)1Mhep)
|
increased hepatocyte proliferation
|
J:92999
|
Tg(K6ODCtr)55Tgo/0
(involves: C3H * C57BL/6)
|
increased keratinocyte apoptosis
|
J:133302
|
Tg(K6ODCtr)55Tgo/0 Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C3H * C57BL/6)
|
cellular phenotype
|
J:133302
|
Tg(K18-ACE2)2Prlmn/0
(B6.Cg-Tg(K18-ACE2)2Prlmn/J)
|
increased lung apoptosis
|
J:294084
|
Tg(KRT5-Akt1*)Jmpa/0
(involves: C57BL/6 * DBA/2 * DBA/2J * FVB/N)
|
decreased keratinocyte proliferation
|
J:144831
|
increased cell proliferation
|
J:144831
|
Tg(KRT5-CDK4)2303Mlrp/0
(involves: FVB * SSIN)
|
abnormal cell morphology
|
J:108690
|
Tg(KRT5-cre)1Tak/Tg(KRT5-cre)1Tak
(involves: C3H * C57BL/6 * FVB/N)
|
cellular phenotype
|
J:120797
|
maternal effect
|
J:120797
|
Tg(KRT5-cre/ERT2)2Ipc/0 Upf3atm1.1Wilk/Upf3atm1.1Wilk
(involves: 129 * 129S4/SvJaeSor * C57BL/6 * SJL)
|
abnormal cell physiology
|
J:234504
|
Tg(KRT5-cre/PGR)1Der/0 Trp63tm2Brd/Trp63tm3.1Brd
(involves: 129S7/SvEvBrd * FVB * ICR)
|
early cellular replicative senescence
|
J:100483
|
Tg(KRT5-IKBKB)1Armz/0
(involves: C57BL/6 * DBA/2)
|
decreased keratinocyte apoptosis
|
J:160072
|
Tg(KRT5-IKBKB)2Armz/0
(involves: C57BL/6 * DBA/2)
|
increased keratinocyte proliferation
|
J:160072
|
Tg(KRT5-rtTA)1Glk/0 Tg(tetO-Tfrc/EGFP/Ova)#Sfz/0 Tg(tetO/CMV-Tslp)#Sfz/0
(involves: C3H * C57BL/6 * FVB/N)
|
increased T cell proliferation
|
J:199558
|
Tg(KRT5-rtTA)1Glk/0 Tg(tetO-TGFB1*C223S*C225S)1Glk/0
(involves: FVB/N)
|
abnormal cell proliferation
|
J:70670
|
decreased cell proliferation
|
J:70670
|
increased keratinocyte apoptosis
|
J:70670
|
Tg(KRT5-rtTA)1Glk/0 Tg(tetO/CMV-Tslp)#Sfz/0
(C.Cg-Tg(KRT5-rtTA)1Glk Tg(tetO/CMV-Tslp)#Sfz)
|
increased B cell proliferation
|
J:182756
|
Tg(KRT5-rtTA)#Glk/0 Tg(tetO-cre)1Jaw/0 Wnt10atm1Smr/Wnt10atm1Smr
(involves: 129X1/SvJ * C57BL/6 * FVB/N)
|
decreased cell proliferation
|
J:242196
|
Tg(KRT5-rtTA)#Glk/0 Tg(tetO-Mir31)#Zhyu/0
(involves: C57BL/6J * FVB/N)
|
increased mammary gland epithelial cell proliferation
|
J:271420
|
Tg(KRT5-Stat3*A661C*N663C)1Jdg/0
(involves: FVB)
|
increased keratinocyte proliferation
|
J:95458
|
Tg(KRT5-Terf2)PMBlas/Y
(involves: C57BL/6 * CBA)
|
abnormal DNA repair
|
J:102653
|
abnormal telomere morphology
|
J:102653
|
chromosomal instability
|
J:102653
|
decreased keratinocyte proliferation
|
J:102653
|
decreased telomere length
|
J:102653
|
increased cellular sensitivity to alkylating agents
|
J:102653
|
increased cellular sensitivity to ultraviolet irradiation
|
J:102653
|
induced chromosome breakage
|
J:102653
|
Tg(KRT5-Terf2)PMBlas/Y Tg(KRT5-Tert)8043Blas/0
(involves: C57BL/6 * CBA * DBA/2)
|
decreased telomere length
|
J:102653
|
Tg(KRT5-Terf2)PNBlas/0
(involves: C57BL/6 * CBA)
|
decreased telomere length
|
J:102653
|
Tg(KRT5-Terf2)POBlas/0
(involves: C57BL/6 * CBA)
|
abnormal DNA repair
|
J:102653
|
chromosomal instability
|
J:102653
|
decreased telomere length
|
J:102653
|
increased cellular sensitivity to alkylating agents
|
J:102653
|
increased cellular sensitivity to ultraviolet irradiation
|
J:102653
|
induced chromosome breakage
|
J:102653
|
Tg(KRT5-Tert)8043Blas/0
(involves: C57BL/6 * DBA/2)
|
cellular phenotype
|
J:69757
|
Tg(KRT5-TGFB1)F2020Xjw/0
(involves: C57BL/6 * DBA/2 * ICR)
|
abnormal basement membrane morphology
|
J:90118
|
decreased keratinocyte proliferation
|
J:90118
|
Tg(KRT5-tTA)1216Glk/0 Tg(tetO-TGFB1*C223S*C225S)1Glk/0
(involves: FVB/N)
|
decreased cell proliferation
|
J:70670
|
Tg(KRT14-CASP1)1Miz/0
(involves: C57BL/6)
|
increased keratinocyte apoptosis
|
J:79706
|
Tg(KRT14-cre)8Brn/0 Tg(KRT5-Akt1*)Jmpa/0 Trp53tm1Brn/Trp53tm1Brn
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * DBA/2J * FVB/N)
|
increased cell proliferation
|
J:144831
|
increased keratinocyte proliferation
|
J:144831
|
Tg(KRT14-Esr1/HRAS)1Pkha/0 Trim27Gt(XP0484)Wtsi/Trim27Gt(XP0484)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
early cellular replicative senescence
|
J:189317
|
Tg(KRT14-Fyn*)aJsey/0
(involves: C57BL/6 * CBA * FVB/N)
|
abnormal keratinocyte differentiation
|
J:155536
|
Tg(KRT14-HPV16)wt1Dh/0
(FVB.Cg-Tg(KRT14-HPV16)wt1Dh/Nci)
|
increased keratinocyte proliferation
|
J:65699
|
Tg(KRT14-HPV16E7)2304Plam/0
(involves: FVB/N)
|
abnormal cell cycle checkpoint function
|
J:101623
|
increased hair follicle apoptosis
|
J:86018
|
Tg(KRT14-HPV16E7)2350Plam/0
(involves: FVB/N)
|
increased hair follicle apoptosis
|
J:86018
|
Tg(KRT14-Il4)#Lsch/0
(involves: BALB/cBy * C57BL/6)
|
increased mast cell degranulation
|
J:126285
|
Tg(KRT14-Kremen1)1Smr/0 Tg(KRT5-rtTA)#Glk/0 Tg(tetO-Dkk1)1Smr/0
(involves: C57BL/6 * FVB/N * SJL)
|
increased hair follicle apoptosis
|
J:204142
|
Tg(Krt14-Nog)#Jake/0
(FVB-Tg(Krt14-Nog)#Jake)
|
abnormal interdigital cell death
|
J:78767
|
Tg(Krt14-Nog)#Jake/0
(involves: BALB/c * C57BL/6 * FVB)
|
abnormal interdigital cell death
|
J:78767
|
Tg(KRT14-rtTA)F42Efu/0 Tg(tetO-EDN1,-lacZ)9Mhus/0
(involves: C57BL/6J * FVB)
|
abnormal melanocyte differentiation
|
J:231435
|
abnormal melanocyte proliferation
|
J:231435
|
Tg(KRT14-rtTA)F42Efu/0 Tg(tetO-GJB2*G45E,-EGFP)#Tww/0
(involves: FVB/N * SKH1)
|
increased hair follicle apoptosis
|
J:220589
|
Tg(KRT14-Snai1)1Efu/0
(involves: CD-1)
|
decreased sensitivity to induced cell death
|
J:229072
|
increased keratinocyte proliferation
|
J:229072
|
Tg(KRT14-Vegfa)3Dtm/0
(FVB/N-Tg(KRT14-Vegfa)3Dtm)
|
abnormal leukocyte adhesion
|
J:104245
|
enhanced leukocyte tethering or rolling
|
J:104245
|
Tg(KRT14-VP16/NR1I2)13Sdub/?
(involves: C57BL/6)
|
abnormal dendritic cell migration
|
J:258435
|
increased keratinocyte proliferation
|
J:258435
|
Tg(LANA,vFLIP,vCYC)801Dtmr/?
(involves: C57BL/6)
|
increased B cell proliferation
|
J:196403
|
Tg(Lck-Akt1*)M-1Pnt/0
(involves: C3H/He * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:73487
|
Tg(Lck-Akt1*E40K)E-3Pnt/0
(involves: C3H/He * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:73487
|
Tg(Lck-Bcl2l1)1Cant/?
(B6.Cg-Tg(Lck-Bcl2l1)1Cant)
|
increased T cell proliferation
|
J:77507
|
Tg(Lck-CrmA)1Hed/0
(involves: BALB/c * C57BL/6J)
|
decreased T cell apoptosis
|
J:100451
|
Tg(Lck-CrmA)1Hed/?
(involves: BALB/c * C57BL/6J)
|
decreased thymocyte apoptosis
|
J:100451
|
Tg(Lck-Cxadr)1Jdgr/0
(FVB-Tg(Lck-Cxadr)1Jdgr)
|
decreased T cell apoptosis
|
J:109884
|
decreased T cell proliferation
|
J:109884
|
Tg(Lck-FADD)1Hed/0
(involves: BALB/c * C57BL/6)
|
abnormal T cell proliferation
|
J:100451
|
Tg(Lck-FADD)1Hed/?
(involves: BALB/c * C57BL/6)
|
decreased thymocyte apoptosis
|
J:100451
|
Tg(LCK-NFKBIA)5Dwb/0
(involves: C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:93003
|
increased T cell apoptosis
|
J:93003
|
Tg(Lck-Socs3)1Kubo/0
(Not Specified)
|
decreased T cell proliferation
|
J:128797
|
Tg(Lck-Sox13)#Jskg/0
(involves: C57BL/6)
|
decreased T cell proliferation
|
J:117301
|
increased thymocyte apoptosis
|
J:117301
|
Tg(Lck-Stat5b*)1Mafa/0
(Not Specified)
|
increased B cell proliferation
|
J:132669
|
Tg(Lck-Stk17b)26.1Wals/?
(B6.Cg-Tg(Lck-Stk17b)26.1Wals)
|
increased T cell proliferation
|
J:149973
|
Tg(Lck-Tnfsf4)1Nish/0
(B6.Cg-Tg(Lck-Tnfsf4)1Nish)
|
increased T cell proliferation
|
J:80214
|
Tg(Lck-TNFSF13)3919Mhah/0
(B6.Cg-Tg(Lck-TNFSF13)3919Mhah)
|
decreased B cell apoptosis
|
J:94628
|
Tg(Lck-Tnfsf14)24Yxf/?
(C57BL/6-Tg(Lck-Tnfsf14)24Yxf)
|
increased enterocyte apoptosis
|
J:128976
|
increased T cell proliferation
|
J:129951
|
Tg(Lck-Tnfsf15,-EGFP)#Targ/0
(involves: C57BL/6)
|
abnormal intestinal goblet cell morphology
|
J:169462
|
Tg(Lck-Tslp)1Chea/0
(B6.Cg-Tg(Lck-Tslp)1Chea)
|
mesangial cell interposition
|
J:72982
|
Tg(Lck/Emu-Rftn1)1Ayos/?
(involves: C57BL/6)
|
increased T cell proliferation
|
J:150299
|
Tg(LckIl4)1315Dbl/0
(involves: C57BL/6J * DBA/2J)
|
abnormal osteoblast physiology
|
J:107359
|
Tg(LCKprBCL2)36Sjk/?
(involves: C3H * C57BL/6)
|
decreased T cell apoptosis
|
J:11548
|
Tg(LCKprBCL2)36Sjk/0
(involves: C57BL/6 * CBA/J)
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(LCKprBCL2)36Sjk/0 Tg(Nr4a1-EGFP/cre)820Khog/0
(involves: C57BL/6 * C57BL/6J)
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(LCKprBCL2)36Sjk/0 Tg(TcraH-Y,TcrbH-Y)71Vbo/0
(involves: C57BL/6 * C57BL/6J * DBA/2J)
|
decreased thymocyte apoptosis
|
J:217939
|
Tg(LCR-HBA2,LCR-HBB*)1Cos/0
(involves: C57BL/6J * CBA/J)
|
maternal effect
|
J:94193
|
Tg(Lgi1)#Mpan/0
(Not Specified)
|
abnormal axon pruning
|
J:154129
|
Tg(Lgi1*)#Mpan/0
(Not Specified)
|
abnormal axon pruning
|
J:154129
|
Tg(LONP1-mt-ND4*,-mCherry*)#Jguy
(B6(D2)-Tg(LONP1-mt-ND4*,-mCherry*)#Jguy)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:224897
|
abnormal oxidative phosphorylation
|
J:224897
|
abnormal retina apoptosis
|
J:224897
|
oxidative stress
|
J:224897
|
Tg(LRRK2)1Cjli/0
(FVB/N-Tg(LRRK2)1Cjli/J)
|
abnormal autophagy
|
J:194153
|
Tg(LRRK2*G2019S)1Cjli/0
(FVB/N-Tg(LRRK2*G2019S)1Cjli/J)
|
abnormal autophagy
|
J:194153
|
Tg(LRRK2*G2019S)1Mjfa/0
(FVB-Tg(LRRK2*G2019S)1Mjfa)
|
abnormal axon extension
|
J:172418
|
Tg(LRRK2*Y1699C)#aMjfa/0
(FVB-Tg(LRRK2*Y1699C)#aMjfa)
|
abnormal axon extension
|
J:172418
|
Tg(Ly6a-BCR/ABL1)IS1AIsg/0
(involves: C57BL/6J * CBA)
|
abnormal chromosome morphology
|
J:144382
|
Tg(Ly6a-BCR/ABL1)IS1BIsg/0
(involves: C57BL/6J * CBA)
|
abnormal chromosome morphology
|
J:144382
|
Tg(Ly6a-GCSAM)102AIsg/0
(involves: C57BL/6J * CBA)
|
increased B cell proliferation
|
J:221238
|
Tg(Ly6a-SET/NUP214)2969Gcg/0
(involves: FVB/NJ)
|
increased B cell apoptosis
|
J:142938
|
Tg(Mbp-SNCA)29Ema/0
(involves: C57BL/6 * DBA/2)
|
abnormal mitochondrial crista morphology
|
J:102867
|
abnormal mitochondrial morphology
|
J:102867
|
abnormal mitochondrial shape
|
J:102867
|
increased mitochondrial size
|
J:102867
|
Tg(MCL1)8Caig/0
(involves: C57BL/6 * SJL)
|
abnormal macrophage apoptosis
|
J:95913
|
abnormal mast cell differentiation
|
J:50604
|
abnormal monocyte differentiation
|
J:50604
|
decreased B cell apoptosis
|
J:50604
|
decreased splenocyte apoptosis
|
J:50604
|
decreased T cell apoptosis
|
J:50604
|
Tg(ML5sHEL)5Ccg/0 Tg(TcrHEL3A9)1Mmd/0
(involves: C57BL/6 * C57BL/10 * C57BR/cd)
|
abnormal T cell proliferation
|
J:78309
|
Tg(ML5sHEL)5Ccg/0 Tg(TcrHEL3A9)1Mmd/0 Tg(TLK2mHEL)2Ccg/0
(involves: C57BL/6JSfd * C57BL/10 * C57BR/cd)
|
abnormal T cell proliferation
|
J:78309
|
Tg(MMTV-AURKA)#Cxd/?
(involves: FVB/N)
|
polyploidy
|
J:145680
|
Tg(MMTV-AURKA)#Cxd/? Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas * FVB/N)
|
polyploidy
|
J:145680
|
Tg(MMTV-cre)1Mam/?
(involves: FVB)
|
maternal effect
|
J:168531
|
Tg(MMTV-cre)4Mam/?
(involves: FVB)
|
maternal effect
|
J:168531
|
Tg(MMTV-cre)FMam/?
(involves: FVB)
|
maternal effect
|
J:168531
|
Tg(MMTV-ERBB2*,-luc)6180Aami/0
(FVB-Tg(MMTV-ERBB2*,-luc)6180Aami)
|
maternal effect
|
J:172352
|
Tg(MMTV-Espl1)1Pati/0
(involves: C57BL/6)
|
abnormal chromosome morphology
|
J:216267
|
aneuploidy
|
J:216267
|
chromosomal instability
|
J:216267
|
Tg(MMTV-NCOA3)#Mybr/0
(FVB/N-Tg(MMTV-NCOA3)#Mybr)
|
decreased mammary gland epithelial cell proliferation
|
J:93548
|
Tg(MMTV-Notch4)3Rnc/0
(involves: FVB/N)
|
oligozoospermia
|
J:11644
|
Tg(MMTV-PyVT)#Mul/0
(B6.FVB-Tg(MMTV-PyVT)#Mul)
|
decreased B cell proliferation
|
J:147923
|
decreased splenocyte proliferation
|
J:147923
|
decreased T cell proliferation
|
J:147923
|
Tg(MMTV-rtTA)1Lach/0 Tg(tetO-MYC)1Lach/0
(involves: FVB)
|
increased mammary gland epithelial cell proliferation
|
J:67498
|
Tg(MMTVneu)202Mul/0 Tg(Trp53R172H)8512Jmr/0
(involves: FVB)
|
aneuploidy
|
J:40336
|
polyploidy
|
J:40336
|
Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc/0
(Not Specified)
|
abnormal mitochondrial morphology
|
J:132035
|
Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc/Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc
(Not Specified)
|
abnormal mitochondrial morphology
|
J:132035
|
Tg(Mpz-RAF1/ESR1)A668Ayld/0
(involves: C57BL/6J * CBA/J)
|
increased Schwann cell proliferation
|
J:182703
|
Tg(Mt1-Hgf)19Lmb/0
(involves: C57BL/6 * FVB/N)
|
abnormal melanoblast migration
|
J:34022
|
Tg(MT2A-Myc)#Misu/0
(C57BL/6-Tg(MT2A-Myc)#Misu)
|
azoospermia
|
J:121355
|
Tg(MT2A-TGFBR2)#Rser/0
(involves: C57BL/6 * DBA)
|
abnormal cell proliferation
|
J:158480
|
Tg(MtTGFA)42Lmb/Tg(MtTGFA)42Lmb
(involves: CD-1)
|
increased hepatocyte karyomegaly
|
J:28452
|
increased mesangial cell number
|
J:20315
|
Tg(Mup3-Plau)350-2Eps/?
(C57BL/6-Tg(Mup3-Plau)350-2Eps)
|
abnormal endoplasmic reticulum morphology
|
J:233146
|
increased hepatocyte apoptosis
|
J:233146
|
Tg(Myh6*/tetO-BAG3)69Atsa/0 Tg(Myh6-tTA)55Rbns/0
(involves: C57BL/6CrSlc * FVB/NJ)
|
abnormal autophagy
|
J:273465
|
Tg(Myh6*/tetO-Hspb8*K141N)#Atsa/0 Tg(Myh6-tTA)55Rbns/0
(involves: C57BL/6CrSlc * FVB/NJ)
|
abnormal oxidative phosphorylation
|
J:197853
|
Tg(Myh6-1810058I24Rik)#Eno/0
(involves: C57BL/6)
|
abnormal mitochondrial morphology
|
J:325962
|
abnormal mitochondrial physiology
|
J:325962
|
cardiac interstitial fibrosis
|
J:325962
|
oxidative stress
|
J:325962
|
Tg(Myh6-ACE2)1Rbre/0
(involves: FVB/N)
|
cardiac interstitial fibrosis
|
J:128793
|
Tg(Myh6-ACE2)2Rbre/0
(involves: FVB/N)
|
cardiac interstitial fibrosis
|
J:128793
|
Tg(Myh6-Acsl1)O7Jesc/0
(FVB/N-Tg(Myh6-Acsl1)O7Jesc)
|
cardiac interstitial fibrosis
|
J:68639
|
increased cardiomyocyte apoptosis
|
J:68639
|
Tg(Myh6-ACTC1*E99K)#Sbm/0
(involves: C57BL/10 * CBA/Ca)
|
cardiac interstitial fibrosis
|
J:175388
|
Tg(Myh6-Actc1*R312H)307Iko/?
(involves: C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:178587
|
Tg(Myh6-Actc1dt)2Kwan/0
(involves: C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:297375
|
Tg(Myh6-Adra1a)A1A4Rmgr/0
(FVB/N-Tg(Myh6-Adra1a)A1A4Rmgr)
|
increased cardiomyocyte apoptosis
|
J:108867
|
Tg(Myh6-Akt1*T308D*S473D)1Siz/0
(Not Specified)
|
cardiac interstitial fibrosis
|
J:75780
|
Tg(Myh6-ANKRD1)#Camm/0
(involves: FVB)
|
abnormal fetal cardiomyocyte mitochondrial morphology
|
J:302922
|
abnormal myocardial fiber mitochondrial morphology
|
J:302922
|
Tg(Myh6-BAG3*P209L)#Mswi/0
(involves: C57BL/6 * DBA/2)
|
decreased mitochondrial size
|
J:234278
|
increased mitochondrial number
|
J:234278
|
Tg(Myh6-Bclaf1)#Cya/0
(Not Specified)
|
increased cardiomyocyte apoptosis
|
J:301260
|
Tg(Myh6-CACNA1C)M1Aschw/0
(involves: FVB/N)
|
cardiac interstitial fibrosis
|
J:134761
|
increased cardiomyocyte apoptosis
|
J:134761
|
Tg(Myh6-cre)TG9Pjay/0
(involves: FVB/N)
|
increased cardiomyocyte apoptosis
|
J:198043
|
Tg(Myh6-Dyrk1b)#Yax/0
(involves: C57BL/6J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:334531
|
abnormal mitochondrial physiology
|
J:334531
|
abnormal myocardial fiber mitochondrial morphology
|
J:334531
|
Tg(Myh6-EGFP/AC3I)#Mean/0
(Not Specified)
|
decreased apoptosis
|
J:207291
|
Tg(Myh6-Erbb2)6Kaga/0
(involves: C57BL/6J * SJL/J)
|
cardiac interstitial fibrosis
|
J:189979
|
Tg(Myh6-GFP,MAP2K3)58Ywa/? Myl2tm1(cre)Krc/Myl2+
(involves: 129S1/Sv * 129X1/SvJ)
|
cardiac interstitial fibrosis
|
J:72242
|
Tg(Myh6-GFP,MAP2K6)8Ywa/? Myl2tm1(cre)Krc/Myl2+
(involves: 129S1/Sv * 129X1/SvJ)
|
cardiac interstitial fibrosis
|
J:72242
|
Tg(Myh6-Gnaq)#Gwd/0
(involves: FVB/N)
|
increased cardiomyocyte apoptosis
|
J:145086
|
Tg(Myh6-Gnaq)#Gwd/0 Tg(Myh6-tTA)55Rbns/0 Tg(tetO-Bnip3l)1Gwd/0
(involves: FVB/N)
|
increased cardiomyocyte apoptosis
|
J:145086
|
Tg(Myh6-Gnaq*Q209L)44Ejne/Tg(Myh6-Gnaq*Q209L)44Ejne
(involves: FVB)
|
cardiac interstitial fibrosis
|
J:127756
|
Tg(Myh6-Gnaq*Q209L)52Ejne/?
(involves: FVB)
|
cardiac interstitial fibrosis
|
J:204274
|
Tg(Myh6-HBEGF)#Iko/0
(involves: C57BL/6 * DBA/2)
|
cardiac interstitial fibrosis
|
J:93335
|
Tg(Myh6-Htr2b)1Lum/0
(involves: CD-1)
|
abnormal mitochondrial morphology
|
J:128784
|
abnormal mitochondrial shape
|
J:128784
|
abnormal oxidative phosphorylation
|
J:128784
|
abnormal respiratory electron transport chain
|
J:128784
|
increased mitochondrial fission
|
J:128784
|
increased mitochondrial number
|
J:128784
|
Tg(Myh6-Jup)2Ajm/0
(involves: FVB/N)
|
cardiac interstitial fibrosis
|
J:192719
|
Tg(Myh6-Jup*)1Ajm/0
(involves: FVB/N)
|
abnormal fat cell differentiation
|
J:192719
|
cardiac interstitial fibrosis
|
J:192719
|
Tg(Myh6-JUP*)1Dpju/0
(FVB/N-Tg(Myh6-JUP*)1Dpju)
|
increased cardiomyocyte apoptosis
|
J:235770
|
Tg(Myh6-LMNA*E82K)35Lizh/0
(involves: C57BL/6J)
|
abnormal mitochondrial physiology
|
J:167734
|
cardiac interstitial fibrosis
|
J:167734
|
increased cardiomyocyte apoptosis
|
J:167734
|
increased mitochondrial size
|
J:167734
|
Tg(Myh6-Map2k1*)1Jmol/?
(involves: FVB)
|
decreased cardiomyocyte apoptosis
|
J:66102
|
Tg(Myh6-Map2k1*)1Jmol/?
(involves: FVB/N)
|
decreased cardiomyocyte apoptosis
|
J:127872
|
Tg(Myh6-Map2k3*)1Jmol/0
(FVB-Tg(Myh6-Map2k3*)1Jmol)
|
cardiac interstitial fibrosis
|
J:83547
|
Tg(Myh6-Map2k7)1Jmol/0
(involves: FVB/N)
|
decreased cardiomyocyte apoptosis
|
J:102152
|
Tg(Myh6-Mapk8*,Myh6-Mapk9*)22.4Jmol/0
(involves: FVB/N)
|
decreased cardiomyocyte apoptosis
|
J:102152
|
Tg(Myh6-Mapk14*)1Jmol/0
(FVB-Tg(Myh6-Mapk14*)1Jmol)
|
cardiac interstitial fibrosis
|
J:83547
|
Tg(Myh6-Mir30c-1)AEec/0
(involves: C57BL/6JOlaHsd * FVB/N)
|
cardiac interstitial fibrosis
|
J:216095
|
Tg(Myh6-Mir30c-1)BEec/0
(involves: C57BL/6JOlaHsd * FVB/N)
|
abnormal mitochondrial physiology
|
J:216095
|
cardiac interstitial fibrosis
|
J:216095
|
Tg(Myh6-Mtg1)3Ywxu/0
(involves: C57BL/6J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:271147
|
Tg(Myh6-Murc)#Tue/0
(Not Specified)
|
cardiac interstitial fibrosis
|
J:136004
|
Tg(Myh6-Mybpc3*)24Rbns/0
(Not Specified)
|
abnormal myocardial fiber mitochondrial morphology
|
J:59702
|
Tg(Myh6-MYH7B)#Lnwd/0
(C57BL/6-Tg(Myh6-MYH7B)#Lnwd)
|
cellular phenotype
|
J:285433
|
Tg(Myh6-MYL2*K104E)2Dsc/0
(involves: C57BL/6 * SJL)
|
increased mitochondrial number
|
J:263776
|
Tg(Myh6-MYL3*A57G)#Dsc/0
(involves: C57BL/6 * SJL)
|
cardiac interstitial fibrosis
|
J:202154,
J:178377
|
Tg(Myh6-MYOZ2*I246M)#Ajm/0
(involves: FVB)
|
cardiac interstitial fibrosis
|
J:210073
|
Tg(Myh6-MYOZ2*S48P)114Ajm/0
(involves: FVB)
|
cardiac interstitial fibrosis
|
J:210073
|
Tg(Myh6-Nox4)#Jusa/0
(FVB-Tg(Myh6-Nox4)#Jusa)
|
abnormal mitochondrial physiology
|
J:163751
|
cardiac interstitial fibrosis
|
J:164275
|
increased cardiomyocyte apoptosis
|
J:163751,
J:164275
|
oxidative stress
|
J:163751
|
Tg(Myh6-Pfkfb3)7Pne/0
(FVB-Tg(Myh6-Pfkfb3)7Pne)
|
decreased cardiac muscle cell glucose uptake
|
J:94475
|
Tg(Myh6-Pln*)#Egk/0
(Not Specified)
|
cardiac interstitial fibrosis
|
J:105976
|
Tg(Myh6-Pln*R9C)#Ces/0
(involves: FVB/N)
|
cardiac interstitial fibrosis
|
J:82353
|
Tg(Myh6-POLG*Y955C)DWcc/0
(Not Specified)
|
abnormal mitochondrial crista morphology
|
J:122507
|
abnormal myocardial fiber mitochondrial morphology
|
J:122507
|
decreased myocardial fiber mitochondrial DNA content
|
J:122507
|
oxidative stress
|
J:122507
|
Tg(Myh6-Ppara)404-3Dpk/0
(involves: C57BL/6 * CBA/J)
|
decreased cardiac muscle cell glucose uptake
|
J:110580
|
Tg(Myh6-Ppard)HEDpk/0
(involves: C57BL/6 * CBA)
|
increased cardiac muscle cell glucose uptake
|
J:130750
|
Tg(Myh6-Ppif)26.2Jmol/0
(FVB/N-Tg(Myh6-Ppif)26.2Jmol)
|
abnormal mitochondrial crista morphology
|
J:97660
|
abnormal myocardial fiber mitochondrial morphology
|
J:97660
|
dilated mitochondrion
|
J:97660
|
increased apoptosis
|
J:97660
|
Tg(Myh6-Ppp3ca)37Eno/0
(involves: FVB)
|
cardiac interstitial fibrosis
|
J:93176
|
Tg(Myh6-Rest*)474Ysai/0
(involves: C57BL/6J)
|
cardiac interstitial fibrosis
|
J:86837
|
Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-Fgfr3*R248C/Fgfr1)#Dor/0
(involves: 129 * C57BL/6 * FVB/N * FVB/NTac)
|
cardiac interstitial fibrosis
|
J:211151
|
Tg(Myh6-rtTA)8585Jam/0 Tg(tetO-Ppargc1a)1Dpk/0
(involves: FVB/N * FVB/NTac)
|
abnormal mitochondrial morphology
|
J:96614
|
increased mitochondrial fission
|
J:96614
|
Tg(Myh6-Rxra)41Pcn/0
(Not Specified)
|
abnormal respiratory electron transport chain
|
J:60351
|
Tg(Myh6-SLC2A1)54Rti/0
(FVB-Tg(Myh6-SLC2A1)54Rti)
|
increased cardiac muscle cell glucose uptake
|
J:106467
|
Tg(Myh6-SOD2,Tyr)3Pne/0
(FVB-Tg(Myh6-SOD2,Tyr)3Pne)
|
abnormal cell physiology
|
J:106815
|
Tg(Myh6-STK4)28Jusa/0
(involves: C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:139414
|
Tg(Myh6-STK4*K59R)10Jusa/0
(involves: C57BL/6)
|
decreased cardiomyocyte apoptosis
|
J:139414
|
Tg(Myh6-Sumo2*)9606Jwang/0
(either: B6.FVB-Tg(Myh6-Sumo2*)9606Jwang or (involves: C57BL/6 * FVB/N))
|
increased cardiomyocyte apoptosis
|
J:230540
|
Tg(Myh6-Sumo2*)9610Jwang/0
(either: B6.FVB-Tg(Myh6-Sumo2*)9610Jwang or (involves: C57BL/6 * FVB/N))
|
cardiac interstitial fibrosis
|
J:230540
|
Tg(Myh6-Tcap)#Rnk/0
(Not Specified)
|
decreased cardiomyocyte apoptosis
|
J:188832
|
Tg(Myh6-TNNI3*G203S)1Chs/0
(Not Specified)
|
cardiac interstitial fibrosis
|
J:114537
|
Tg(Myh6-TNNI3*G203S)4Chs/0
(Not Specified)
|
cardiac interstitial fibrosis
|
J:114537
|
Tg(Myh6-Tnni3*R146G)121Rbns/0
(Not Specified)
|
cardiac interstitial fibrosis
|
J:243628
|
Tg(Myh6-Tnni3*R146G)133Rbns/0
(Not Specified)
|
abnormal myocardial fiber mitochondrial morphology
|
J:243628
|
cardiac interstitial fibrosis
|
J:243628
|
Tg(Myh6-TNNI3K)#Tfo/0
(involves: FVB/N)
|
oxidative stress
|
J:213546
|
Tg(Myh6-TNNI3K*K490R)#Tfo/0
(involves: FVB/N)
|
cellular phenotype
|
J:213546
|
Tg(Myh6-Tnnt2*R92Q)2Lnwd/0
(involves: C57BL/6)
|
cardiac interstitial fibrosis
|
J:56911
|
Tg(Myh6-Tnnt2*R92Q)3Lnwd/0
(involves: C57BL/6)
|
cardiac interstitial fibrosis
|
J:56911
|
Tg(Myh6-TNNT2*R92Q)#Ajm/0
(involves: C3H * C57BL/6 * ICR)
|
cardiac interstitial fibrosis
|
J:161899,
J:162685
|
Tg(Myh6-TNNT2*R141W)#Ajm/0
(involves: C3H * C57BL/6 * ICR)
|
cardiac interstitial fibrosis
|
J:161899
|
Tg(Myh6-TNNT2*R141W)#Lian/0
(involves: C57BL/6J)
|
cardiac interstitial fibrosis
|
J:211769
|
Tg(Myh6-Tpm1*E54K)67Dfw/0
(involves: FVB/N)
|
cardiac interstitial fibrosis
|
J:137813
|
Tg(Myh6-tTA)6Smbf/0 Tg(tetO-DTA)1Gfi/0
(involves: C57BL/6 * CBA)
|
increased cardiomyocyte apoptosis
|
J:128617
|
Tg(Myh6-tTA)6Smbf/0 Tg(tetO-Mir208a)#Dzw/0
(involves: C3H * C57BL/6 * CBA)
|
cardiac interstitial fibrosis
|
J:152696
|
Tg(Myh6-tTA)6Smbf/0 Tg(tetO-NOS2,-lacZ)240iMhus/0
(involves: C57BL/6 * CBA)
|
cardiac interstitial fibrosis
|
J:132082
|
Tg(Myh6-tTA)55Rbns/? Tg(Myh6/tetO-BNIP3)1Gwd/?
(Not Specified)
|
increased cardiomyocyte apoptosis
|
J:127533
|
Tg(Myh6-tTA)55Rbns/0 Tg(tetO-Bnip3l)1Gwd/0
(involves: FVB/N)
|
increased cardiomyocyte apoptosis
|
J:145086
|
Tg(Myh6-tTA)55Rbns/0 Tg(tetO-Dusp6)1Jmol/0
(involves: FVB/N)
|
increased cardiomyocyte apoptosis
|
J:124903
|
Tg(Myh6-Yap1*S112A)#Eno/0
(involves: C3H * C57BL/6)
|
decreased cardiomyocyte apoptosis
|
J:200670
|
Tg(Myh7-BVp35-EGFP)#Ksa/?
(involves: C3H * C57BL/6)
|
abnormal cardiomyocyte apoptosis
|
J:102279
|
Tg(Myh7-Phc1)#Yota/0
(involves: C57BL/6)
|
abnormal mitochondrial crista morphology
|
J:75968
|
abnormal mitochondrial shape
|
J:75968
|
increased cardiomyocyte apoptosis
|
J:75968
|
Tg(Myh7-Pln)2Egk/0
(FVB/N-Tg(Myh7-Pln)2Egk)
|
oxidative stress
|
J:224766
|
Tg(Myh7-Ptpn11*Q510E)#Krnz/0
(FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz)
|
cardiac interstitial fibrosis
|
J:181656
|
Tg(Myl1-SOD1*G93A)#Amu/0
(FVB/NJ-Tg(Myl1-SOD1*G93A)#Amu)
|
abnormal mitochondrial crista morphology
|
J:143747
|
abnormal mitochondrial morphology
|
J:143747
|
abnormal mitochondrial shape
|
J:143747
|
increased mitochondrial size
|
J:143747
|
oxidative stress
|
J:143747
|
Tg(Myl1-Trp53inp2)1Azo/0
(involves: C57BL/6J)
|
enhanced autophagy
|
J:212763
|
Tg(Myl1-Trp53inp2)2Azo/0
(involves: C57BL/6J)
|
enhanced autophagy
|
J:212763
|
Tg(Myl2-FGF19)1Dfre/?
(involves: FVB)
|
increased hepatocyte proliferation
|
J:77160
|
Tg(Myl2SLC2A1)2Mue/0
(involves: C57BL/6 * SJL)
|
increased skeletal muscle cell glucose uptake
|
J:93868
|
Tg(MYOC*Y437H)#Sit/0
(B6.FVB-Tg(MYOC*T437C)#Sit)
|
abnormal axon fasciculation
|
J:135177
|
Tg(Nell1)1Ting/0
(involves: C3H * C57BL/6)
|
enhanced osteoblast differentiation
|
J:79106
|
Tg(Neph1-Vegfa)1Seq/0
(Not Specified)
|
abnormal mesangial cell morphology
|
J:82440
|
detached podocyte
|
J:82440
|
Tg(Nes-cre)1Kln/0 Tg(ACTB-NOTCH1)1Shn/0
(B6.Cg-Tg(Nes-cre)1Kln Tg(ACTB-NOTCH1)1Shn)
|
abnormal neuron apoptosis
|
J:90392
|
Tg(Nes-cre)1Kln/0 Triotm1Mzhu/Triotm1Mzhu
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal cerebellar granule cell migration
|
J:165902
|
abnormal neuron differentiation
|
J:165902
|
increased neuron apoptosis
|
J:165902
|
Tg(Nes-cre)1Kln/0 Ube4bem1Bcgen/Ube4bem1Bcgen
(involves: C57BL/6N * SJL)
|
decreased neuronal precursor proliferation
|
J:332423
|
Tg(Nes-cre)1Kln/0 Wdr45btm1c(EUCOMM)Hmgu/Wdr45btm1c(EUCOMM)Hmgu
(involves: C57BL/6 * SJL)
|
abnormal Golgi apparatus morphology
|
J:298097
|
cellular phenotype
|
J:298097
|
dilated mitochondrion
|
J:298097
|
Tg(Nes-cre)1Kln/0 Zfp568tm1Ckjs/Zfp568tm1Ckjs
(involves: C57BL/6J * SJL)
|
abnormal neuronal precursor proliferation
|
J:192224
|
Tg(Nes-cre)1Wme/Tg(Nes-cre)1Wme
(involves: C57BL/6 * CBA)
|
abnormal neuronal precursor cell migration
|
J:112466
|
aneuploidy
|
J:112466
|
decreased neuronal precursor proliferation
|
J:112466
|
increased neuron apoptosis
|
J:112466
|
Tg(Nes-cre/ERT2)1Imayo/0
(involves: C57BL/6)
|
decreased neuronal precursor proliferation
|
J:112466
|
Tg(Nes-cre/ERT2)4Imayo/0
(involves: C57BL/6)
|
decreased neuronal precursor proliferation
|
J:112466
|
Tg(NES/TK-PDGFB,-lacZ)310Kfn/0
(involves: C57BL/6 * CBA)
|
increased apoptosis
|
J:165035
|
Tg(NES/TK-PDGFB,-lacZ)310Kfn/0
(B6.Cg-Tg(NES/TK-PDGFB,-lacZ)310Kfn)
|
increased retina apoptosis
|
J:189829
|
Tg(Neurod2-Smo*A2)#Jols/0
(C57BL/6-Tg(Neurod2-Smo*A2)#Jols)
|
abnormal neuron proliferation
|
J:189258
|
abnormal neuronal migration
|
J:189258
|
abnormal radial glial cell morphology
|
J:189258
|
Tg(Nr5a1-cre)2Klp/0 Trim28tm1.1Ipc/Trim28tm1.1Ipc
(involves: 129S * 129S2/SvPas * C57BL/6J * DBA/2J)
|
cellular phenotype
|
J:327192
|
Tg(Omp-Hist2h2be)14Dlc/0
(involves: C57BL/6)
|
increased neuron apoptosis
|
J:197878
|
Tg(PDGFB-Hyou1)#Tam/0
(involves: BALB/c * C57BL/6)
|
decreased susceptibility to neuronal excitotoxicity
|
J:91396
|
Tg(PDGFB-LRRK2*G2019S)340Djmo/0
(involves: C3H/HeJ * C57BL/6J)
|
abnormal autophagy
|
J:171645
|
Tg(PDGFB-LRRK2*R1441C)574Djmo/0
(involves: C3H/HeJ * C57BL/6J)
|
abnormal autophagy
|
J:171645
|
Tg(PDGFB-SNCA/EGFP)78Ema/0
(involves: C57BL/6 * DBA/2)
|
abnormal lysosome morphology
|
J:238692
|
Tg(PDGFB-UCHL1*I93M)LWada/0
(involves: C57BL/6J)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:128045
|
Tg(PF4MER)6Kra/?
(FVB/N-Tg(PF4MER)6Kra)
|
abnormal megakaryocyte differentiation
|
J:35507
|
Tg(PGK1-FTL*)#Sle/0
(involves: FVB/N)
|
oxidative stress
|
J:227451
|
Tg(PGK1-FTL*)#Sle/0
(B6J.FVB-Tg(PGK1-FTL*)#Sle)
|
oxidative stress
|
J:227451
|
Tg(Pgk-tetR,tetO-RNAi:Pum3)#Yuj/0 Tg(Pou5f1-EGFP)2Mnn/0
(involves: C57BL/6 * C57BL/6J * CBA/CaJ)
|
abnormal primordial germ cell migration
|
J:338852
|
abnormal primordial germ cell morphology
|
J:338852
|
decreased primordial germ cell number
|
J:338852
|
decreased primordial germ cell proliferation
|
J:338852
|
Tg(Pkd1)6Mtru/0
(involves: C57BL/6J * CBA/J)
|
increased hepatocyte proliferation
|
J:157952
|
increased kidney cell proliferation
|
J:157952
|
Tg(Pkd1)26Mtru/0
(involves: C57BL/6J * CBA/J)
|
increased hepatocyte proliferation
|
J:157952
|
increased kidney cell proliferation
|
J:157952
|
Tg(Plp1-Eif2ak3*)18Pop/Tg(Plp1-Eif2ak3*)18Pop
(C57BL/6J-Tg(Plp1-Eif2ak3*)18Pop)
|
abnormal translation
|
J:216298
|
Tg(Plp)66Kan/Tg(Plp)66Kan
(B6NCrl.Cg-Tg(Plp)66Kan)
|
abnormal oligodendrocyte apoptosis
|
J:156106
|
Tg(Plp)72Kan/Tg(Plp)72Kan
(B6N.Cg-Tg(Plp)72Kan)
|
abnormal cell cytoskeleton morphology
|
J:229229
|
Tg(PML-RARA)556Kog/?
(involves: FVB/N)
|
abnormal neutrophil differentiation
|
J:39327
|
Tg(Prm1-Tfam)4Lrsn/?
(involves: FVB/N)
|
cellular phenotype
|
J:95207
|
Tg(Prnp-Abca1)EHol/0
(involves: C57BL/6 * CBA)
|
multinucleated giant male germ cells
|
J:131400
|
Tg(Prnp-ATXN3)BVcg/Tg(Prnp-ATXN3)BVcg
(involves: C3H/HeJ * C57BL/6)
|
azoospermia
|
J:121039
|
increased male germ cell apoptosis
|
J:121039
|
Tg(Prnp-FUS*R521C)3313Ejh/0
(involves: C57BL/6 * SJL)
|
abnormal cell physiology
|
J:209419
|
Tg(Prnp-HTRA2)1Olri/0
(involves: C57BL/6)
|
abnormal cell physiology
|
J:229160
|
abnormal mitochondrial physiology
|
J:229160
|
Tg(Prnp-HTRA2*G399S)1Olri/0
(involves: C57BL/6)
|
abnormal mitochondrial physiology
|
J:229160
|
Tg(Prnp-Immt/SOD1*G93A)7Gmnf/0
(involves: C57BL/6 * CBA * SJL)
|
abnormal mitochondrial morphology
|
J:177846
|
disorganized mitochondrial cristae
|
J:177846
|
Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf
(involves: C57BL/6 * CBA * SJL)
|
abnormal mitochondrial morphology
|
J:177846
|
abnormal mitochondrial physiology
|
J:177846
|
disorganized mitochondrial cristae
|
J:177846
|
Tg(Prnp-MAPT*P301S)50Hiw/0
(B6.Cg-Tg(Prnp-MAPT*P301S)50Hiw)
|
abnormal cell physiology
|
J:213361
|
Tg(Prnp-PFN1*C71G)22Zxu/0 Tg(Thy1-PFN1*C71G)67Zxu/Tg(Thy1-PFN1*C71G)67Zxu
(involves: FVB/N)
|
abnormal cell cytoskeleton morphology
|
J:235427
|
Tg(Prnp-PSEN2*N141I)30Jgr/0 Tg(Thy1-APPSwe)71Jgr/0
(B6.Cg-Tg(Prnp-PSEN2*N141I)30Jgr Tg(Thy1-APPSwe)71Jgr)
|
abnormal neuron differentiation
|
J:165986
|
Tg(Prnp-SETX*R2136H)1920Als/0
(involves: C57BL/6J)
|
increased susceptibility to neuronal excitotoxicity
|
J:320844
|
Tg(Prnp-TARDBP*Q331K)103Dwc/0
(B6.Cg-Tg(Prnp-TARDBP*Q331K)103Dwc/J)
|
oxidative stress
|
J:242322
|
Tg(Prnp-UBQLN2)WT-hiHlp/0
(involves: C57BL/6 * SJL)
|
cellular phenotype
|
J:299301
|
Tg(Prnp-UBQLN2)WT-lowHlp/0
(involves: C57BL/6 * SJL)
|
cellular phenotype
|
J:299301
|
Tg(Prnp-UBQLN2*P506T)#Hlp/0
(involves: C57BL/6 * SJL)
|
cellular phenotype
|
J:299301
|
Tg(Prp-GPR37)1Ryot/0
(involves: C3H * C57BL/6)
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:128745
|
oxidative stress
|
J:140326
|
Tg(Pten)1Srn/0
(involves: C57BL/6 * CBA)
|
abnormal cell physiology
|
J:182671
|
decreased cell proliferation
|
J:182671
|
increased adipocyte glucose uptake
|
J:182671
|
Tg(RCAN1)M9Mapr/?
(involves: C57BL/6 * CBA)
|
abnormal neuron differentiation
|
J:184606
|
Tg(Rnu6-RNAi:Bccip)4Zshn/0
(FVB/N-Tg(Rnu6-RNAi:Bccip)4Zshn)
|
abnormal double-strand DNA break repair
|
J:176115
|
chromosomal instability
|
J:176115
|
decreased cell proliferation
|
J:176115
|
increased cellular sensitivity to gamma-irradiation
|
J:176115
|
Tg(RNU6-RNAi:Mpp5)13Wij/0 Tg(rx3-icre)1Mjam/0
(involves: 129P2/OlaHsd * C57BL/6 * FVB/N)
|
increased neuron apoptosis
|
J:178056
|
Tg(RNU6-RNAi:Rhox3)2Wilk/0 Tg(Stra8-icre)1Reb/0
(involves: FVB/NJ)
|
abnormal male meiosis
|
J:229199
|
abnormal spermatid morphology
|
J:229199
|
decreased male germ cell number
|
J:229199
|
increased male germ cell apoptosis
|
J:229199
|
oligozoospermia
|
J:229199
|
Tg(RP3-340H11)29Kel/0
(involves: C57BL/6J * CBA/Ca)
|
paternal imprinting
|
J:91709
|
Tg(S100a4-TK)M31Egn/0
(involves: BALB/c * C57BL/6 * SJL)
|
decreased sensitivity to induced cell death
|
J:160213
|
increased sensitivity to induced cell death
|
J:160213
|
Tg(Scgb1a1-Has2)1Nbl/0
(C57BL/6J-Tg(Scgb1a1-Has2)1Nbl)
|
decreased apoptosis
|
J:102879
|
Tg(Scgb1a1-rtTA)1Jaw/0 Tg(tetO-Aimp1)29872Mcla/0
(involves: 129 * C57BL/6)
|
increased lung endothelial cell apoptosis
|
J:173904
|
Tg(Scgb1a1-rtTA,-tTS,tetO-CHI3L1)1Eli/0
(Not Specified)
|
decreased apoptosis
|
J:148490
|
decreased T cell apoptosis
|
J:148490
|
Tg(Scgb1a1-rtTA,tetO-Ifng)14Eli/0
(involves: C57BL/6 * CBA)
|
increased apoptosis
|
J:100854
|
Tg(SERPINA1-Tnfsf12)1Biib/0
(involves: C57BL/6 * DBA/2)
|
increased hepatocyte apoptosis
|
J:100907
|
Tg(SERPINC1-SV40)A1Pbr/0
(involves: C57BL/6 * DBA/2)
|
abnormal cell nucleus morphology
|
J:101541
|
Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-Fgf9,-EGFP)#Dor/0
(involves: FVB)
|
increased mesenchymal cell proliferation involved in lung development
|
J:224791
|
Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-PLAGL2)P3Ysy/0
(involves: FVB/N)
|
increased apoptosis
|
J:152422
|
Tg(Shh)#Dje/0
(involves: Swiss Webster)
|
abnormal cell proliferation
|
J:94461
|
Tg(SOD1)2Gur/0 Tg(SOD1*L126Z)#Deng/0
(involves: C57BL/6 * SJL)
|
abnormal mitochondrial crista morphology
|
J:109458
|
Tg(SOD1*G37R)9Dpr/0
(involves: C3H/HeJ * C57BL/6J)
|
abnormal motor neuron mitochondrial morphology
|
J:69178
|
Tg(SOD1*G37R)29Dpr/0
(involves: C3H/HeJ * C57BL/6J)
|
abnormal motor neuron mitochondrial morphology
|
J:69178
|
Tg(SOD1*G37R)42Dpr/0
(involves: C3H/HeJ * C57BL/6J)
|
abnormal motor neuron mitochondrial morphology
|
J:69178
|
Tg(SOD1*G37R)106Dpr/0
(involves: C3H/HeJ * C57BL/6J)
|
abnormal motor neuron mitochondrial morphology
|
J:69178
|
Tg(SOD1*G85R/EYFP)737Alho/Tg(SOD1*G85R/EYFP)737Alho
(involves: C57BL/6J * SJL/J)
|
abnormal autophagy
|
J:212250
|
Tg(SOD1*G93A)1Gur/0
(involves: C57BL/6 * SJL)
|
abnormal cell physiology
|
J:61249
|
decreased cellular glucose uptake
|
J:61249
|
increased cellular sensitivity to oxidative stress
|
J:61249
|
Tg(SOD1*G93A)1Gur/0
(B6SJL-Tg(SOD1*G93A)1Gur/J)
|
abnormal cell physiology
|
J:103582,
J:129976
|
abnormal endoplasmic reticulum morphology
|
J:146652,
J:165019
|
abnormal mitochondrial crista morphology
|
J:146652
|
abnormal mitochondrial morphology
|
J:165019
|
abnormal mitochondrial physiology
|
J:158298
|
abnormal mitochondrial shape
|
J:129976
|
abnormal respiratory electron transport chain
|
J:129976
|
dilated mitochondrion
|
J:146652
|
increased mitochondrial size
|
J:158298
|
Tg(SOD1*G93A)1Gur/0
(B6SJL-Tg(SOD1*G93A)1Gur)
|
abnormal mitochondrial morphology
|
J:144199
|
Tg(SOD1*G93A)2Gur/0
(involves: C57BL/6 * SJL)
|
abnormal endoplasmic reticulum morphology
|
J:78629
|
abnormal mitochondrial morphology
|
J:78629
|
Tg(SOD1*G93A)dl1Gur/0
(involves: C57BL/6 * CBA * SJL)
|
abnormal mitochondrial morphology
|
J:134095
|
Tg(Sox3)1Pqt/0 Tg(Sox3-EGFP)NrPqt/0
(involves: C57BL/6 * CBA)
|
increased cell proliferation
|
J:184232
|
Tg(Sox3-GFP,Tyr)HolNpln/Tg(Sox3-GFP,Tyr)HolNpln
(involves: FVB/N)
|
abnormal enteric neural crest cell migration
|
J:229828
|
Tg(SREBP1a)7343Reh/?
(involves: 129 * C57BL/6 * C57BL/6J * SJL)
|
increased mesangial cell number
|
J:93775
|
Tg(SRY-YFP,Tyr)TashTNpln/Tg(SRY-YFP,Tyr)TashTNpln
(involves: FVB/N)
|
abnormal cell differentiation
|
J:224231
|
abnormal enteric neural crest cell migration
|
J:224231
|
abnormal neural crest cell physiology
|
J:224231
|
Tg(Stra8-icre)1Reb/0 Upf3atm1.1Wilk/Upf3a+
(involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ)
|
abnormal spermatocyte morphology
|
J:234504
|
decreased male germ cell number
|
J:234504
|
Tg(Stra8-icre)1Reb/0 Zscan21tm1.1Jiwa/Zscan21tm1.1Jiwa
(involves: FVB/NJ)
|
abnormal double-strand DNA break repair
|
J:237046
|
abnormal spermatocyte morphology
|
J:237046
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:237046
|
arrest of male meiosis
|
J:237046
|
decreased round spermatid number
|
J:237046
|
Tg(SULT1A1,SULT1A2)1Glatt/0
(FVB/N-Tg(SULT1A1,SULT1A2)1Glatt)
|
abnormal cell physiology
|
J:217578
|
Tg(Tagln-Ager)#Yon/?
(C57BL/6-Tg(Tagln-Ager)#Yon)
|
decreased vascular smooth muscle cell proliferation
|
J:82620
|
Tg(Tagln-tTA)1Mrab/0 Tg(tetO-Mcpt1)1Mrab/0
(involves: C57BL/6 * SJL)
|
increased cell proliferation
|
J:70031
|
Tg(TCF/Lef1-lacZ)34Efu/0
(Not Specified)
|
abnormal keratinocyte differentiation
|
J:102493
|
Tg(Tcra2D2,Tcrb2D2)1Kuch/0
(involves: C57BL/6)
|
increased cell proliferation
|
J:83278
|
Tg(Tcra2D2,Tcrb2D2)1Kuch/0
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased T cell proliferation
|
J:189919
|
increased T cell apoptosis
|
J:189919
|
increased T cell proliferation
|
J:189919
|
Tg(Tcra,Tcrb)3Ayr/0
(involves: C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:80775
|
Tg(Tcra,Tcrb)24Efro/0
(D1.Cg-Tg(Tcra,Tcrb)24Efro)
|
decreased T cell proliferation
|
J:104243
|
increased T cell proliferation
|
J:104243
|
Tg(TcrAND)53Hed/?
(involves: A/WySnSg * C57BL/6 * C57BL/10SnSg * SJL)
|
abnormal T cell proliferation
|
J:85777
|
Tg(TcraR28,TcrbR28)KRNDim/0
(involves: C57BL/6 * NOD * SJL)
|
abnormal macrophage chemotaxis
|
J:36815
|
abnormal T cell proliferation
|
J:36815
|
Tg(TcraTcrb)425Cbn/0 Trim30atm1Yjk/Trim30atm1Yjk
(involves: 129P2/OlaHsd * BALB/c * C57BL/6)
|
increased T cell proliferation
|
J:215171
|
Tg(TcraTcrb)1100Mjb/?
(involves: C57BL/6)
|
increased T cell proliferation
|
J:92867
|
Tg(TcraTcrb)1100Mjb/?
(involves: C57BL/6 * MRL/Mp)
|
increased hepatocyte apoptosis
|
J:72817
|
Tg(TcrHEL3A9)1Mmd/0
(involves: C57BL/6)
|
increased T cell proliferation
|
J:73608
|
Tg(TcrHEL3A9)1Mmd/0
(involves: C57BL/6 * C57BL/10 * C57BR/cd)
|
abnormal T cell proliferation
|
J:78309
|
Tg(TcrHEL3A9)1Mmd/0 Tg(TLK2mHEL)2Ccg/0
(involves: C57BL/6 * C57BL/10 * C57BR/cd)
|
abnormal T cell proliferation
|
J:78309
|
Tg(TcrLCMV)327Sdz/0
(involves: C57BL/6 * DBA/2)
|
decreased T cell proliferation
|
J:77696
|
Tg(Tek-Jam3)1Maal/?
(B6.Cg-Tg(Tek-Jam3)1Maal)
|
abnormal cellular extravasation
|
J:99020
|
abnormal leukocyte adhesion
|
J:99020
|
impaired neutrophil chemotaxis
|
J:99020
|
Tg(Tek-tTA)1Rwng/0 Tg(tetO-Notch4*)1Rwng/0
(involves: FVB/N)
|
increased neuron apoptosis
|
J:139943
|
Tg(TERT)C10Hode/0
(involves: C57BL/6 * SPRET/Ei)
|
abnormal telomere length
|
J:92243
|
Tg(tetO-BCR/ABL1)2Dgt/0 Tg(MMTVtTA)1Mam/0
(involves: C57BL/6 * FVB/N * SJL)
|
increased apoptosis
|
J:72377
|
Tg(tetO-BCR/ABL1)27Dgt/0 Tg(MMTVtTA)1Mam/0
(involves: C57BL/6 * FVB/N * SJL)
|
increased apoptosis
|
J:72377
|
Tg(tetO-Mir24-1)#Smoc/0 Tg(KRT14-rtTA)F42Efu/0
(involves: FVB)
|
decreased keratinocyte proliferation
|
J:306624
|
Tg(tetO-Xbp1_is)#Pesch/0 Tg(Adipoq-rtTA)2Zvw/0
(involves: C57BL/6 * C57BL/6N * FVB/N)
|
increased fatty acid oxidation
|
J:260830
|
Tg(tetO/CMV-Prnp*,-lacZ)33Mjy/0 Tg(Camk2a-rtTA)1237Kndl/0
(involves: FVB/N)
|
abnormal plasma membrane morphology
|
J:153494
|
Tg(tetO/CMV-Prnp*,-lacZ)33Mjy/Tg(tetO/CMV-Prnp*,-lacZ)33Mjy Tg(Camk2a-rtTA)1237Kndl/0
(involves: FVB/N)
|
abnormal cell morphology
|
J:153494
|
abnormal plasma membrane morphology
|
J:153494
|
Tg(TetOp-Polb/tTA)2Sbl/0
(B6.Cg-Tg(TetOp-Polb/tTA)2Sbl)
|
increased mesangial cell number
|
J:152481
|
Tg(Th-SNCA*)1.2Ccs/?
(involves: C57BL/6)
|
abnormal mitochondrial morphology
|
J:127707,
J:127708,
J:168847
|
abnormal mitochondrial physiology
|
J:168847
|
Tg(Th-Twnk*,-EGFP)2Gcor/0
(involves: C57BL/6J)
|
abnormal autophagy
|
J:188914
|
abnormal cell physiology
|
J:188914
|
abnormal mitochondrial morphology
|
J:188914
|
abnormal mitochondrial physiology
|
J:188914
|
Tg(Thy1-App*R609D*K612E)2Vln/0
(involves: C57BL * CBA/J)
|
increased neuron apoptosis
|
J:32213
|
Tg(Thy1-App*R609D*K612E)4Vln/0
(involves: FVB)
|
increased neuron apoptosis
|
J:32213
|
Tg(Thy1-APPSL)28Lpr/0
(involves: C57BL/6 * CBA)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:152956
|
Tg(Thy1-APPDutch)#Jckr/0
(involves: C57BL/6J)
|
abnormal basement membrane morphology
|
J:92796
|
Tg(Thy1-APPSw,Thy1-PSEN1*L166P)21Jckr/?
(involves: C57BL/6)
|
abnormal cell physiology
|
J:234763
|
Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz/0
(C57BL/6-Tg(Thy1-APPSwe,Prnp-PSEN2*N141I)152HLaoz)
|
abnormal neuron differentiation
|
J:165986
|
Tg(Thy1-BSCL2*N88S)1Dit/0
(involves: C57BL/6 * DBA/2)
|
increased endoplasmic reticulum stress
|
J:175537
|
Tg(Thy1-EGFP)MJrs/0 Trim9tm1.1Slgu/Trim9tm1.1Slgu
(involves: 129S4/SvJae * BALB/cJ * C57BL/6J * CBA)
|
abnormal neuron differentiation
|
J:215804
|
Tg(Thy1-MAPT)1Vln/Tg(Thy1-MAPT)1Vln
(involves: FVB)
|
abnormal cell cytoskeleton morphology
|
J:100971
|
Tg(Thy1-MAPT)2Vln/Tg(Thy1-MAPT)2Vln
(involves: FVB)
|
abnormal cell cytoskeleton morphology
|
J:100971
|
Tg(Thy1-Snca)1S13Putt/?
(involves: C57BL/6)
|
increased mitochondrial size
|
J:177661
|
Tg(THY1-SNCA*A30P)M30Sud/0
(Not Specified)
|
increased neuron apoptosis
|
J:139867
|
Tg(THY1-SNCA*A53T)F53Sud/0
(involves: C57BL/6)
|
increased neuron apoptosis
|
J:140019
|
Tg(THY1-SNCA*A53T)M53Sud/0
(B6.Cg-Tg(THY1-SNCA*A53T)M53Sud/J)
|
increased neuron apoptosis
|
J:212732
|
Tg(Thy1-SOD1*G93A)T1Hgrd/0 Tg(Thy1-SOD1*G93A)T3Hgrd/0
(involves: C57BL/6 * CBA * FVB)
|
cellular phenotype
|
J:134095
|
Tg(Thy1-SOD1*G93A)T3Hgrd/Tg(Thy1-SOD1*G93A)T3Hgrd
(involves: C57BL/6 * CBA * FVB)
|
cellular phenotype
|
J:134095
|
Tg(Thy1-TARDBP)6Singh/Tg(Thy1-TARDBP)6Singh
(involves: C57BL/6 * C57BL/6J * SJL)
|
increased neuron apoptosis
|
J:157550
|
Tg(Thy1-TARDBP*)BOddo/0
(C57BL/6-Tg(Thy1-TARDBP*)BOddo)
|
abnormal autophagy
|
J:223932
|
Tg(Thy1-TARDBP*)BOddo/Tg(Thy1-TARDBP*)BOddo
(C57BL/6-Tg(Thy1-TARDBP*)BOddo)
|
abnormal autophagy
|
J:223932
|
Tg(Thy1/THY1)T6Gsv/0
(involves: C57BL/10 * CBA)
|
increased macrophage derived foam cell number
|
J:294621
|
X/Tg(Tlr7)6Boll
(involves: C57BL/6)
|
increased splenocyte proliferation
|
J:127600
|
Tg(TNF)197Gkl/0
(involves: C57BL/6 * CBA)
|
abnormal osteoclast differentiation
|
J:97992
|
Tg(TNF)3647Gkl/0
(involves: C57BL/6 * CBA)
|
impaired osteoblast differentiation
|
J:190204
|
Tg(Tnf)6074Gkl/0
(involves: C57BL/6 * CBA)
|
abnormal oligodendrocyte apoptosis
|
J:106592
|
Tg(Tnf)6074Gkl/0 Tnfrsf1btm1Mwm/Tnfrsf1btm1Mwm
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
abnormal oligodendrocyte apoptosis
|
J:106592
|
Tg(Tnfsf13b)1Fma/0 Tnfsf14tm1Kpf/Tnfsf14tm1Kpf
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2J)
|
abnormal mesangial cell morphology
|
J:114782
|
Tg(Tnfsf13b)1Fma/Tg(Tnfsf13b)1Fma
(involves: C57BL/6 * DBA/2)
|
abnormal mesangial cell morphology
|
J:178227
|
Tg(Tnnt2-TNNT2*R92Q)#Ajm/0
(involves: C3H * C57BL/6 * ICR)
|
cardiac interstitial fibrosis
|
J:117554
|
Tg(Tnnt2-TNNT2*R92Q)M-2Ajm/0
(involves: C3H * C57BL/6 * ICR)
|
cardiac interstitial fibrosis
|
J:117554
|
Tg(Trp53)1Srn/0
(involves: C57BL/6 * CBA)
|
increased thymocyte apoptosis
|
J:80311
|
Tg(Trp53)1Srn/0 Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
decreased thymocyte apoptosis
|
J:80311
|
Tg(TRP53)4Dgj/0 Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * FVB)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:162466
|
Tg(Trp53)bSrn/0
(involves: C57BL/6 * CBA)
|
increased thymocyte apoptosis
|
J:80311
|
Tg(TRP53*R72P)7Dgj/0 Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * FVB)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:162466
|
Tg(Trp53R172H)8512Jmr/0
(involves: FVB)
|
chromosomal instability
|
J:46426
|
Tg(TSPY1-Figla)#Dean/?
(FVB/N-Tg(TSPY1-Figla)#Dean)
|
abnormal chromatoid body morphology
|
J:162655
|
abnormal sperm motility
|
J:162655
|
abnormal spermatocyte morphology
|
J:162655
|
arrest of male meiosis
|
J:162655
|
decreased male germ cell number
|
J:162655
|
kinked sperm flagellum
|
J:162655
|
oligozoospermia
|
J:162655
|
Tg(Ttr-Cdkn1a)36Tvd/?
(B6.Cg-Tg(Ttr-Cdkn1a)36Tvd)
|
decreased hepatocyte proliferation
|
J:94077
|
Tg(Ttr-KLF6)1Fdmn/?
(Not Specified)
|
decreased hepatocyte proliferation
|
J:122903
|
Tg(Tyr-NRAS*Q61K)1Bee/0
(involves: C57BL/6J * DBA/2)
|
abnormal melanocyte proliferation
|
J:193443
|
Tg(UAS-Shh)1Rth/0 Tg(Wnt1-GAL4)1Rth/0
(involves: C57BL/6J * CBA/J)
|
increased cell proliferation
|
J:57948
|
Tg(Ubc-Fto)#Pzg/0
(involves: C57BL/6J)
|
decreased oligodendrocyte progenitor number
|
J:301796
|
Tg(Umod*C147W)958Lura/0
(involves: FVB)
|
increased kidney cell proliferation
|
J:161532
|
Tg(Umod*C217G)1Xrw/0
(involves: FVB/N)
|
increased renal tubule apoptosis
|
J:252420
|
Tg(Vav1-Lin28b)C3Apla/0
(involves: C57BL/6)
|
increased T cell proliferation
|
J:189197
|
Tg(Vav1-STAT5B*N642H)726Biat/0
(C57BL/6NCrl-Tg(Vav1-STAT5B*N642H)726Biat)
|
increased T cell proliferation
|
J:257519
|
Tg(Vil1-Lin28b,-tdTomato)HiAru/0
(involves: C57BL/6J * SJL)
|
abnormal intestinal goblet cell morphology
|
J:202923
|
Tg(Vil1-PPARGC1A)#Amos/0
(involves: FVB/N)
|
increased enterocyte apoptosis
|
J:171361
|
increased mitochondrial number
|
J:171361
|
Tg(Vil-SLC3A2)HEMerl/0
(involves: FVB/N)
|
abnormal enterocyte proliferation
|
J:173946
|
Tg(Vim*R113C)1Tmm/0
(B6.CBA-Tg(Vim*R113C)1Tmm)
|
abnormal cell morphology
|
J:145782
|
Tg(WTbeta2)4Wjk/?
(Not Specified)
|
cardiac interstitial fibrosis
|
J:128583
|
Tg(YAC18)18Hay/0
(involves: FVB/N)
|
decreased susceptibility to neuronal excitotoxicity
|
J:144917
|
Tg(YAC72)2511Hay/0
(involves: FVB/N)
|
increased susceptibility to neuronal excitotoxicity
|
J:144917
|
Tg(YAC72)2511Hay/Tg(YAC72)2511Hay
(FVB/N-Tg(YAC72)2511Hay)
|
increased neuron apoptosis
|
J:105728
|
increased susceptibility to neuronal excitotoxicity
|
J:105728
|
Tg(YAC128)53Hay/0
(FVB/N-Tg(YAC128)53Hay)
|
increased susceptibility to neuronal excitotoxicity
|
J:105723
|
Tg(YAC128)55Hay/0
(FVB/N-Tg(YAC128)55Hay)
|
increased susceptibility to neuronal excitotoxicity
|
J:105723
|
Tg(YAC128)55Hay/Tg(YAC128)55Hay
(FVB/N-Tg(YAC128)55Hay)
|
increased neuron apoptosis
|
J:105728
|
increased susceptibility to neuronal excitotoxicity
|
J:105723,
J:105728
|
Tg(YAC353G6)W7Hay/Tg(YAC353G6)W7Hay
(FVB/NJ-Tg(YAC353G6)W7Hay)
|
decreased susceptibility to neuronal excitotoxicity
|
J:120991
|
Tg(YACW408A5)1952Ricc/0
(involves: 129/Sv * SD7)
|
abnormal imprinting
|
J:96366
|
Tg(Zp3-cre)93Knw/0 Ttktm1Katj/Ttktm1Katj
(involves: 129 * C57BL/6 * C57BL/6J)
|
abnormal female meiosis
|
J:173618
|
abnormal meiotic spindle assembly checkpoint
|
J:173618
|
aneuploidy
|
J:173618
|
enhanced polar body extrusion
|
J:173618
|
Tg(Zp3-cre)93Knw/0 Yy1tm1Yshi/Yy1tm2.1Yshi
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal oocyte morphology
|
J:170240
|
oocyte degeneration
|
J:170240
|
Tg(Zp3-cre)93Knw/0 Zfp57tm1Xjli/Zfp57tm1Xjli
(either: (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * Black Swiss * C57BL/6J))
|
maternal effect
|
J:143283
|
Tgfb1tm1N/Tgfb1tm1N
(involves: 129S/SvEv * C57BL/6J * NIH/Ola)
|
abnormal vascular endothelial cell differentiation
|
J:26913
|
Tgfb2tm1Doe/Tgfb2+
(involves: 129P2/OlaHsd * Black Swiss)
|
oligozoospermia
|
J:78547
|
teratozoospermia
|
J:78547
|
Tgfb2tm1Doe/Tgfb2+
(involves: 129P2/OlaHsd)
|
decreased enterocyte apoptosis
|
J:76342
|
Tgfb2tm1Doe/Tgfb2+ Tgfb3tm1Doe/Tgfb3+
(involves: 129P2/OlaHsd)
|
decreased enterocyte apoptosis
|
J:76342
|
Tgfb2tm1Doe/Tgfb2tm1Doe Tgfb3tm1Doe/Tgfb3+
(involves: 129P2/OlaHsd)
|
abnormal interdigital cell death
|
J:76541
|
decreased retina apoptosis
|
J:105113
|
Tgfb2tm1Doe/Tgfb2tm1Doe Tgfb3tm1Doe/Tgfb3tm1Doe
(involves: 129P2/OlaHsd)
|
abnormal interdigital cell death
|
J:76541
|
abnormal retina apoptosis
|
J:105113
|
Tgfb3tm1Doe/Tgfb3+
(involves: 129P2/OlaHsd)
|
decreased enterocyte apoptosis
|
J:76342
|
Tgfb3tm1Doe/Tgfb3tm1Doe
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased neuron apoptosis
|
J:117465
|
Tgfbitm1.1Nap/Tgfbitm1.1Nap
(B6N.129S(FVB)-Tgfbitm1.1Nap)
|
decreased retina apoptosis
|
J:230754
|
Tgfbitm1Jwu/Tgfbitm1Jwu
(B6.129-Tgfbitm1Jwu)
|
increased pancreatic beta cell apoptosis
|
J:213611
|
Tgfbitm1Zhao/Tgfbitm1Zhao
(involves: 129 * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:143036
|
abnormal chromosome morphology
|
J:143036
|
Tgfbr1tm1.1Karl/Tgfbr1tm1.1Karl Tg(Mx1-cre)1Cgn/0
(involves: 129 * C57BL/6 * CBA)
|
increased hematopoietic stem cell proliferation
|
J:86262
|
Tgfbr2tm1.2Hlm/Tgfbr2tm1.2Hlm H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S6/SvEvTac * C57BL/6J * CBA/J)
|
decreased cranial neural crest cell proliferation
|
J:86042
|
Tgfbr2tm1Sjkm/Tgfbr2+
(Not Specified)
|
increased hepatocyte proliferation
|
J:71591
|
Tgfbr3tm1Stv/Tgfbr3tm1Stv
(involves: 129/Sv * C57BL/6)
|
abnormal fetal cardiomyocyte proliferation
|
J:83727
|
Tgfbr3lem2Djb/Tgfbr3lem2Djb
(C57BL/6N-Tgfbr3lem2Djb)
|
abnormal oocyte number
|
J:316383
|
Tgif1tm1.1Caw/Tgif1tm1.1Caw
(B6.129S-Tgif1tm1.1Caw)
|
increased middle ear goblet cell number
|
J:198238
|
Tgif1tm1Dwot/Tgif1tm1Dwot Tgif2tm1Dwot/Tgif2tm1Dwot
(involves: 129S/SvEv * 129X1/SvJ * C57BL/6J)
|
decreased embryonic epiblast cell proliferation
|
J:157256
|
Tgif1tm1Pah/Tgif1tm1Pah
(involves: 129S/SvEv * CD-1)
|
abnormal cell cycle
|
J:109616
|
decreased cell proliferation
|
J:109616
|
Tgm2tm1.1Rmgr/Tgm2tm1.1Rmgr
(involves: 129S1/SvImJ * C57BL/6)
|
abnormal cell adhesion
|
J:95130
|
Tgm2tm1Gml/Tgm2tm1Gml
(involves: C57BL/6)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:126414,
J:131975
|
Tgm2tm1Gml/Tgm2tm1Gml
(involves: C57BL/6 * DBA/1LacJ)
|
impaired macrophage phagocytosis
|
J:132254
|
Tgs1tm1.1Jkr/Tgs1tm1.1Jkr
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
abnormal cell cycle
|
J:189008
|
impaired fibroblast cell migration
|
J:189008
|
TgTn(pb-CAG-Gm614)#Cya/0
(involves: C57BL/6)
|
decreased B cell apoptosis
|
J:307345
|
Thap1tm1.1Meeh/Thap1tm1.2Meeh
(involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6)
|
abnormal axon extension
|
J:226849
|
Thap1tm1.2Meeh/Thap1tm1.2Meeh
(involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6)
|
abnormal axon extension
|
J:226849
|
Thap11tm1.1Tpz/Thap11tm1.1Tpz
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:136306
|
absent inner cell mass proliferation
|
J:136306
|
Thap11tm1Tpz/Thap11tm1Tpz
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:136306
|
Thbdtm2.1Emc/Thbdtm2.1Emc
(involves: 129/Sv * BALB/c * C57BL/6)
|
abnormal leukocyte adhesion
|
J:118000
|
Thbs1tm1Hyn/Thbs1tm1Hyn
(involves: 129S2/SvPas * C57BL/6)
|
cellular phenotype
|
J:139652
|
increased lacrimal gland apoptosis
|
J:153126
|
Thbs1tm1Hyn/Thbs1tm1Hyn
(involves: 129S2/SvPas)
|
abnormal mitochondrial physiology
|
J:133700
|
decreased renal tubule apoptosis
|
J:104708
|
Thbs1tm1Hyn/Thbs1tm1Hyn Thbs2tm1Bst/Thbs2tm1Bst
(involves: 129T2/SvEms * 129X1/SvJ)
|
impaired macrophage chemotaxis
|
J:78876
|
Thbs2tm1Bst/Thbs2tm1Bst
(either: (involves: 129S4/SvJae * 129X1/SvJ) or (involves: 129X1/SvJ))
|
decreased apoptosis
|
J:69756
|
Them4tm1Hem/Them4tm1Hem
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal hepatocyte mitochondrial morphology
|
J:149552
|
cellular phenotype
|
J:149552
|
Them5tm1Hem/Them5tm1Hem
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cellular respiration
|
J:186657
|
abnormal mitochondrial morphology
|
J:186657
|
abnormal mitochondrial shape
|
J:186657
|
abnormal respiratory electron transport chain
|
J:186657
|
increased mitochondrial size
|
J:186657
|
Themistm1Gasc/Themistm1Gasc
(B6.129S-Themistm1Gasc)
|
decreased T cell proliferation
|
J:151074
|
Themistm1Hasu/Themistm1Hasu
(involves: C57BL/6 * CBA)
|
increased T cell proliferation
|
J:153235
|
Thoc1tm1Dwg/Thoc1tm1Dwg
(involves: 129S4/SvJae)
|
increased embryonic tissue cell apoptosis
|
J:109614
|
Thoc2em1Gecz/Y
(C57BL/6JArc-Thoc2em1Gecz)
|
abnormal intracellular organelle physiology
|
J:345229
|
abnormal mitosis
|
J:345229
|
abnormal neuronal migration
|
J:345229
|
increased apoptosis
|
J:345229
|
premature neuronal precursor differentiation
|
J:345229
|
Thoc6em1Schaf/Thoc6em1Schaf
(C57BL/6JN-Thoc6em1Schaf)
|
increased embryonic tissue cell apoptosis
|
J:345604
|
Thraem1Ffla/Thra+
(C57BL/6-Thraem1Ffla)
|
abnormal enterocyte proliferation
|
J:268664
|
Thraem2Ffla/Thra+
(C57BL/6-Thraem2Ffla)
|
abnormal enterocyte proliferation
|
J:268664
|
Thratm1.1Fcas/Thratm1.1Fcas
(B6.Cg-Thratm1.1Fcas)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:179839
|
Thratm1Jas/Thratm1Jas
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal enterocyte proliferation
|
J:84537
|
abnormal intestinal goblet cell morphology
|
J:84537
|
Thratm1Syc/Thra+
(involves: 129S6/SvEvTac)
|
decreased cardiac muscle cell glucose uptake
|
J:95397
|
Thratm1Ven/Thratm1Ven Thrbtm1Df/Thrbtm1Df
(B6.129-Thratm1Ven Thrbtm1Df)
|
abnormal sperm motility
|
J:117324
|
Thratm2Jas/Thratm2Jas
(involves: 129)
|
abnormal enterocyte proliferation
|
J:84537
|
abnormal intestinal goblet cell morphology
|
J:84537
|
Thratm3Jas/Thratm3Jas
(involves: 129)
|
abnormal enterocyte proliferation
|
J:84537
|
abnormal intestinal goblet cell morphology
|
J:84537
|
Thrap3tm1c(KOMP)Wtsi/Thrap3tm1c(KOMP)Wtsi Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * C57BL/6J * C57BL/6N * DBA)
|
abnormal autophagosome formation
|
J:339439
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:339439
|
abnormal mitochondrial crista morphology
|
J:339439
|
abnormal mitophagy
|
J:339439
|
abnormal respiratory electron transport chain
|
J:339439
|
enhanced autophagy
|
J:339439
|
increased hepatocyte mitochondrial DNA content
|
J:339439
|
increased mitochondrial size
|
J:339439
|
Thrbtm1.1Syc/Thrbtm1.1Syc
(involves: 129S6/SvEvTac)
|
increased cardiac muscle cell glucose uptake
|
J:95397
|
Thypr1DBA/2J/?
(involves: C57BL/6J * DBA/2J)
|
increased T cell proliferation
|
J:76931
|
Thypr2DBA/2J/?
(involves: C57BL/6J * DBA/2J)
|
increased T cell proliferation
|
J:76931
|
Tial1tm1Mst/Tial1tm1Mst
(involves: 129S2/SvPas * C57BL/6)
|
decreased primordial germ cell number
|
J:46239
|
Tiam1tm1Jgc/Tiam1tm1Jgc
(involves: 129P2/OlaHsd * FVB)
|
abnormal apoptosis
|
J:77148
|
decreased cell proliferation
|
J:77148
|
Ticam1Lps2/Ticam1Lps2
(involves: C57BL/6)
|
decreased macrophage apoptosis
|
J:84896,
J:92674
|
Ticam1tm1Aki/Ticam1tm1Aki
(involves: 129P2/OlaHsd)
|
decreased splenocyte proliferation
|
J:84679
|
impaired macrophage phagocytosis
|
J:185198
|
Tifabtm1.1Dsta/Tifab+
(involves: 129 * C57BL/6 * C57BL/6J)
|
decreased hematopoietic stem cell proliferation
|
J:229024
|
Tifabtm1.1Dsta/Tifabtm1.1Dsta
(involves: 129 * C57BL/6 * C57BL/6J)
|
decreased hematopoietic stem cell proliferation
|
J:229024
|
TigarGt(EUCE0047g05)Hmgu/TigarGt(EUCE0047g05)Hmgu
(involves: 129P2/OlaHsd)
|
abnormal small intestinal crypt cell proliferation
|
J:198650
|
increased cellular sensitivity to alkylating agents
|
J:198650
|
increased cellular sensitivity to gamma-irradiation
|
J:198650
|
increased small intestinal crypt cell apoptosis
|
J:198650
|
oxidative stress
|
J:198650
|
Tigartm1.2Smat/Tigartm1.2Smat Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6JJcl * C57BL/6NCrj)
|
abnormal autophagy
|
J:183674
|
abnormal mitochondrial chromosome morphology
|
J:183674
|
abnormal mitochondrial physiology
|
J:183674
|
decreased cardiomyocyte apoptosis
|
J:183674
|
oxidative stress
|
J:183674
|
Tigittm1Sdl/Tigittm1Sdl
(involves: C57BL/6)
|
increased T cell proliferation
|
J:168902
|
Timd4tm1Kuch/Timd4tm1Kuch
(C57BL/6-Timd4tm1Kuch)
|
increased splenocyte proliferation
|
J:160747
|
Timd4tm1Osa/Timd4tm1Osa
(involves: C57BL/6)
|
impaired macrophage phagocytosis
|
J:187181
|
Timd4tm1Wouy/Timd4tm1Wouy
(involves: 129)
|
impaired macrophage phagocytosis
|
J:160304
|
Timp3tm1Rkho/Timp3tm1Rkho
(involves: 129 * C57BL/6)
|
cellular phenotype
|
J:71609
|
Timp3tm1Rkho/Timp3tm1Rkho
(FVB.129-Timp3tm1Rkho)
|
abnormal apoptosis
|
J:71690
|
Timp3tm1Rkho/Timp3tm1Rkho
(B6.129-Timp3tm1Rkho)
|
increased hepatocyte apoptosis
|
J:92948
|
Tincrem1Kei/Tincrem1Kei
(Not Specified)
|
decreased keratinocyte proliferation
|
J:339811
|
Tinf2tm2.2Tdl/Tinf2+
(involves: BALB/cJ * C57BL/6)
|
decreased telomere length
|
J:207367
|
tip/tip
(B6C3Fe a/a-tip/J)
|
abnormal Purkinje cell mitochondrial morphology
|
J:236593
|
Tiraptm1Medz/Tiraptm1Medz
(involves: 129S1/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:96773
|
Tjp1tm1.1Whun/Tjp1tm1.1Whun Tg(Nphs1-cre)33Mska/0
(involves: C57BL/6 * C57BL/6N * DBA/2)
|
detached podocyte
|
J:226210
|
Tjp1tm1.1Whun/Tjp1tm1.1Whun Tjp2tm2Whun/Tjp2tm2Whun Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * C57BL/6NTac * DBA/2)
|
increased hepatocyte proliferation
|
J:306936
|
Tjp1tm1Sats/Tjp1tm1Sats
(B6.Cg-Tjp1tm1Sats)
|
increased allantois apoptosis
|
J:222380
|
increased embryonic tissue cell apoptosis
|
J:222380
|
increased neural tube apoptosis
|
J:222380
|
Tjp2tm1Whun/Tjp2tm1Whun
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6))
|
abnormal plasma membrane morphology
|
J:132649
|
decreased cell proliferation
|
J:132649
|
increased embryonic tissue cell apoptosis
|
J:132649
|
Tk2tm1Anka/Tk2tm1Anka
(involves: 129X1/SvJ * C57BL/6)
|
abnormal mitochondrial crista morphology
|
J:137664
|
decreased mitochondrial DNA content
|
J:137664
|
Tk2tm1Mihi/Tk2tm1Mihi
(involves: 129S6/SvEv * C57BL/6J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:139195
|
decreased mitochondrial DNA content
|
J:139195,
J:166725
|
decreased muscle fiber mitochondrial DNA content
|
J:166725
|
decreased myocardial fiber mitochondrial DNA content
|
J:166725
|
Tle3Gt(XP0165)Wtsi/Tle3Gt(XP0165)Wtsi
(involves: 129P2/OlaHsd)
|
abnormal cell differentiation
|
J:172245
|
Tle3tm1.1Pton/Tle3tm1.1Pton Tle4tm1.1Dasw/Tle4tm1.1Dasw Tg(Pdx1-cre)6Tuv/0
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * FVB/N)
|
abnormal pancreatic beta cell differentiation
|
J:307817
|
decreased pancreatic beta cell proliferation
|
J:307817
|
Tle3tm1Jcc/Tle3tm1Jcc
(involves: 129P2/OlaHsd)
|
abnormal pancreatic alpha cell differentiation
|
J:183486
|
abnormal pancreatic beta cell differentiation
|
J:183486
|
abnormal pancreatic delta cell differentiation
|
J:183486
|
abnormal pancreatic epsilon cell differentiation
|
J:183486
|
abnormal PP cell differentiation
|
J:183486
|
Tle4tm1.2Dasw/Tle4tm1.2Dasw
(B6.129S6(Cg)-Tle4tm1.2Dasw)
|
increased thymocyte apoptosis
|
J:219243
|
Tle6tm1Lil/Tle6tm1Lil
(Not Specified)
|
abnormal microtubule cytoskeleton morphology
|
J:276268
|
abnormal mitotic spindle morphology
|
J:276268
|
Tln1tm4.1Crit/Tln1tm4.1Crit Tln2tm1.1Crit/Tln2tm1.1Crit Tg(ACTA1-cre)1Mll/0
(involves: 129P2/OlaHsd * BALB/cJ)
|
abnormal cell cytoskeleton morphology
|
J:153959
|
abnormal myoblast fusion
|
J:153959
|
Tln2tm2Crit/Tln2tm2Crit
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:190037
|
decreased fibroblast proliferation
|
J:190037
|
Tlq1BALB/c/Tlq1BALB/c
(involves: BALB/c * C57BL/6J * M. spretus)
|
increased telomere length
|
J:48933
|
Tlq1M. spretus/Tlq1BALB/c
(involves: BALB/c * C57BL/6J * M. spretus)
|
increased telomere length
|
J:48933
|
Tlq1M. spretus/Tlq1M. spretus
(involves: BALB/c * C57BL/6J * M. spretus)
|
decreased telomere length
|
J:48933
|
Tlr2tm1Aki/Tlr2tm1Aki
(involves: 129P2/OlaHsd * C57BL/6)
|
cardiac interstitial fibrosis
|
J:103019
|
Tlr2tm1Aki/Tlr2tm1Aki
(B6.129P2-Tlr2tm1Aki)
|
abnormal neuron differentiation
|
J:129957
|
Tlr2tm1Aki/Tlr2tm1Aki
(involves: 129P2/OlaHsd)
|
abnormal leukocyte migration
|
J:171379
|
increased B cell apoptosis
|
J:135830
|
Tlr2tm1Aki/Tlr2tm1Aki Tlr4tm1Aki/Tlr4tm1Aki
(B6.129P2-Tlr2tm1Aki Tlr4tm1Aki)
|
increased apoptosis
|
J:102879
|
Tlr2tm1Kir/Tlr2tm1Kir
(B6.129-Tlr2tm1Kir)
|
abnormal cellular extravasation
|
J:171028
|
decreased neuron apoptosis
|
J:124100
|
decreased splenocyte proliferation
|
J:121930
|
increased adipocyte glucose uptake
|
J:162168
|
Tlr2tm1Kir/Tlr2tm1Kir
(involves: 129)
|
abnormal endoplasmic reticulum morphology
|
J:94463
|
abnormal mitochondrial morphology
|
J:94463
|
abnormal mitochondrial shape
|
J:94463
|
decreased mitochondrial number
|
J:94463
|
Tlr4lps-4Btlr/Tlr4lps-4Btlr
(C57BL/6J-Tlr4lps-4Btlr)
|
decreased macrophage apoptosis
|
J:224664
|
Tlr4lps-7Btlr/Tlr4+
(C57BL/6J-Tlr4Lps-7Btlr)
|
cellular necrosis
|
J:234239
|
increased cell death
|
J:234239
|
Tlr4lps-7Btlr/Tlr4lps-7Btlr
(C57BL/6J-Tlr4Lps-7Btlr)
|
cellular necrosis
|
J:234239
|
increased cell death
|
J:234239
|
Tlr4Lps-8Btlr/Tlr4+
(C57BL/6J-Tlr4Lps-8Btlr)
|
cellular necrosis
|
J:234241
|
increased cell death
|
J:234241
|
Tlr4Lps-8Btlr/Tlr4Lps-8Btlr
(C57BL/6J-Tlr4Lps-8Btlr)
|
cellular necrosis
|
J:234241
|
increased cell death
|
J:234241
|
Tlr4Lps-d/Tlr4Lps-d
(involves: C3H/HeJ)
|
abnormal glial cell apoptosis
|
J:99051
|
abnormal osteoclast differentiation
|
J:131353
|
Tlr4Lps-d/Tlr4Lps-d
(C3H/HeJ-Tlr4Lps-d)
|
abnormal macrophage chemotaxis
|
J:122597
|
abnormal skeletal muscle cell glucose uptake
|
J:126488
|
decreased hepatocyte apoptosis
|
J:135830
|
decreased neuron apoptosis
|
J:124100
|
Tlr4lps-del/Tlr4lps-del
(involves: C57BL/10ScN)
|
abnormal neuron differentiation
|
J:129957
|
Tlr4tm1.1Djh/Tlr4tm1.1Djh
(involves: FVB/N)
|
abnormal enterocyte proliferation
|
J:192520
|
abnormal fibroblast proliferation
|
J:192520
|
Tlr4tm1.1Djh/Tlr4tm1.1Djh
(involves: C57BL/6 * FVB/N * SJL)
|
abnormal enterocyte differentiation
|
J:193668
|
abnormal intestinal goblet cell morphology
|
J:193668
|
Tlr4tm1Aki/Tlr4tm1Aki
(involves: 129P2/OlaHsd * C57BL/6J)
|
impaired neutrophil chemotaxis
|
J:98224
|
Tlr4tm1Aki/Tlr4tm1Aki
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:76115
|
Tlr4tm1Djh/Tlr4tm1Djh Tg(Vil1-cre)997Gum/0
(involves: C57BL/6 * C57BL/6J * FVB/N * SJL)
|
abnormal intestinal goblet cell morphology
|
J:193668
|
Tlr5tm1Flv/Tlr5tm1Flv
(involves: 129S1/Sv)
|
abnormal leukocyte migration
|
J:171379
|
Tlr7em2Anu/Y
(C57BL/6NCrl-Tlr7em2Anu)
|
decreased B cell apoptosis
|
J:324448
|
decreased B cell proliferation
|
J:324448
|
Tlr7tm1Flv/Y
(B6.129S1-Tlr7tm1Flv)
|
decreased splenocyte proliferation
|
J:127600
|
Tlr9m3Btlr/Tlr9m3Btlr
(C57BL/6J-Tlr9m3Btlr)
|
decreased B cell proliferation
|
J:128406
|
Tlr9m4Btlr/Tlr9+
(C57BL/6J-Tlr9m4Btlr)
|
decreased B cell proliferation
|
J:132489
|
Tlr9tm1Aki/Tlr9tm1Aki
(involves: 129P2/OlaHsd)
|
abnormal leukocyte migration
|
J:171379
|
Tlx1tm1Thr/Tlx1tm1Thr
(involves: 129P2/OlaHsd * MF1)
|
increased splenocyte apoptosis
|
J:28700
|
Tm4sf19em1Sjkm/Tm4sf19em1Sjkm
(C57BL/6J-Tm4sf19em1Sjkm)
|
abnormal osteoclast differentiation
|
J:343322
|
Tm4sf19em2Sjkm/Tm4sf19em2Sjkm
(C57BL/6J-Tm4sf19em2Sjkm)
|
abnormal osteoclast differentiation
|
J:343322
|
Tm9sf5em1Dzha/Tm9sf5em1Dzha
(C57BL/6-Tm9sf5em1Dzha)
|
abnormal mitochondrial physiology
|
J:320690
|
abnormal oocyte morphology
|
J:320690
|
aneuploidy
|
J:320690
|
enhanced autophagy
|
J:320690
|
maternal effect
|
J:320690
|
oxidative stress
|
J:320690
|
Tmc7em1Zjl/Tmc7em1Zjl
(C57BL/6J-Tmc7em1Zjl)
|
abnormal acrosome assembly
|
J:359286
|
abnormal acrosome morphology
|
J:359286
|
abnormal male germ cell physiology
|
J:359286
|
abnormal proacrosomal vesicle fusion
|
J:359286
|
abnormal sperm head morphology
|
J:359286
|
increased male germ cell apoptosis
|
J:359286
|
Tmco1em1Smoc/Tmco1em1Smoc
(C57BL/6JSmoc-Tmco1em1Smoc)
|
abnormal osteoblast physiology
|
J:233671
|
Tmco1tm1Tsta/Tmco1tm1Tsta
(B6.Cg-Tmco1tm1Tsta)
|
increased endoplasmic reticulum stress
|
J:268917
|
increased granulosa cell apoptosis
|
J:268917
|
oocyte degeneration
|
J:268917
|
oxidative stress
|
J:268917
|
Tmed10tm1Mjo/Tmed10+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal Golgi apparatus morphology
|
J:95650
|
Tmem41bem1Cya/Tmem41b+
(involves: C57BL/6)
|
impaired autophagy
|
J:316472
|
Tmem53em1Ikeg/Tmem53em1Ikeg
(Not Specified)
|
abnormal osteoblast physiology
|
J:306057
|
enhanced osteoblast differentiation
|
J:306057
|
Tmem64Gt(SYA242)Byg/Tmem64Gt(SYA242)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:198051
|
enhanced osteoblast differentiation
|
J:198051
|
Tmem67tm1Dgen/Tmem67tm1Dgen
(B6.129P2-Tmem67tm1Dgen)
|
abnormal brain ependyma motile cilium morphology
|
J:193837
|
abnormal centrosome morphology
|
J:193837
|
abnormal cilium morphology
|
J:193837
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:176174
|
absent embryonic cilia
|
J:193837
|
cellular phenotype
|
J:176174
|
Tmem68tm1a(EUCOMM)Wtsi/Tmem68tm1a(EUCOMM)Wtsi
(C57BL/6N-Tmem68tm1a(EUCOMM)Wtsi)
|
abnormal lipid oxidation
|
J:339870
|
Tmem70tm1a(KOMP)Wtsi/Tmem70+
(involves: C57BL/6N)
|
cellular phenotype
|
J:238642
|
Tmem70tm1a(KOMP)Wtsi/Tmem70tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal mitochondrial crista morphology
|
J:238642
|
abnormal mitochondrial physiology
|
J:238642
|
abnormal mitochondrial shape
|
J:238642
|
abnormal oxidative phosphorylation
|
J:238642
|
disorganized mitochondrial cristae
|
J:238642
|
oxidative stress
|
J:238642
|
Tmem94em1Mcvm/Tmem94em1Mcvm
(C57BL/6-Tmem94em1Mcvm)
|
abnormal neuronal migration
|
J:269160
|
Tmem102tm1.1Jyen/Tmem102tm1.1Jyen
(B6.Cg-Tmem102tm1.1Jyen)
|
abnormal leukocyte adhesion
|
J:200103
|
decreased cell chemotaxis
|
J:200103
|
impaired leukocyte migration
|
J:200103
|
Tmem106bem1Damme/Tmem106bem1Damme
(C57BL/6-Tmem106bem1Damme)
|
abnormal lysosome morphology
|
J:288278
|
impaired autophagy
|
J:288278
|
Tmem107schlei/Tmem107schlei
(C3Fe.B6-Tmem107schlei)
|
abnormal cilium morphology
|
J:186552
|
Tmem107tm1Lex/Tmem107tm1Lex
(B6N.129S5(Cg)-Tmem107tm1Lex/Mmucd)
|
abnormal primary cilium morphology
|
J:255606
|
Tmem109tm1Yamt/Tmem109tm1Yamt
(B6.Cg-Tmem109tm1Yamt)
|
decreased thymocyte apoptosis
|
J:157864
|
Tmem117tm1.1Thor/Tmem117tm1.1Thor
(involves: C57BL/6N)
|
oxidative stress
|
J:339175
|
Tmem119tm1Tfur/Tmem119tm1Tfur
(involves: 129S6/SvEvTac)
|
impaired osteoblast differentiation
|
J:204884
|
Tmem127tm1.1Pdah/Tmem127tm1.1Pdah
(involves: BALB/cJ * C57BL/6)
|
abnormal cell morphology
|
J:209071
|
abnormal lysosome physiology
|
J:209071
|
Tmem135fun025/Tmem135fun025
(C57BL/6J-Tmem135fun025)
|
abnormal mitochondrial morphology
|
J:237184
|
abnormal mitochondrial physiology
|
J:237184
|
abnormal respiratory electron transport chain
|
J:237184
|
decreased mitochondrial fission
|
J:237184
|
decreased mitochondrial number
|
J:237184
|
increased mitochondrial size
|
J:237184
|
oxidative stress
|
J:237184
|
Tmem160em1.1Bros/Tmem160em1.1Bros
(involves: C57BL/6JRj * FVB/N)
|
cellular phenotype
|
J:328221
|
Tmem161bem1Jgg/Tmem161bem1Jgg
(C57BL/6-Tmem161bem1Jgg)
|
abnormal radial glial cell morphology
|
J:338312
|
Tmem161bem1Jgg/Tmem161bem3Jgg
(C57BL/6-Tmem161bem1Jgg/Tmem161bem3Jgg)
|
abnormal radial glial cell morphology
|
J:338312
|
Tmem161bem2Jgg/Tmem161bem2Jgg
(C57BL/6-Tmem161bem2Jgg)
|
abnormal radial glial cell morphology
|
J:338312
|
Tmem161bem2Jgg/Tmem161bem3Jgg
(C57BL/6-Tmem161bem2Jgg/Tmem161bem3Jgg)
|
abnormal radial glial cell morphology
|
J:338312
|
Tmem175em1Dren/Tmem175+
(B6.Cg-Tmem175em1Dren)
|
abnormal lysosome physiology
|
J:304120
|
Tmem175em1Dren/Tmem175em1Dren
(B6.Cg-Tmem175em1Dren)
|
abnormal autophagy
|
J:304120
|
abnormal lysosome physiology
|
J:304120
|
increased cellular sensitivity to hydrogen peroxide
|
J:304120
|
increased susceptibility to neuronal excitotoxicity
|
J:304120
|
Tmem175em2Dren/Tmem175+
(C57BL/6J-Tmem175em2Dren)
|
abnormal lysosome physiology
|
J:304120
|
Tmem175em2Dren/Tmem175em2Dren
(C57BL/6J-Tmem175em2Dren)
|
abnormal lysosome physiology
|
J:304120
|
decreased cellular sensitivity to hydrogen peroxide
|
J:304120
|
decreased susceptibility to neuronal excitotoxicity
|
J:304120
|
Tmem175em3Dren/Tmem175+
(C57BL/6J-Tmem175em3Dren)
|
abnormal lysosome physiology
|
J:304120
|
increased susceptibility to neuronal excitotoxicity
|
J:304120
|
Tmem175em3Dren/Tmem175em3Dren
(C57BL/6J-Tmem175em3Dren)
|
abnormal lysosome physiology
|
J:304120
|
increased susceptibility to neuronal excitotoxicity
|
J:304120
|
Tmem178tm1Lex/Tmem178tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:228311
|
Tmem182em1Cya/Tmem182em1Cya
(C57BL/6J-Tmem182em1Cya)
|
abnormal cell adhesion
|
J:314094
|
abnormal myoblast differentiation
|
J:314094
|
abnormal myoblast fusion
|
J:314094
|
abnormal myoblast migration
|
J:314094
|
Tmem184bGt(IST10294F4)Tigm/Tmem184bGt(IST10294F4)Tigm
(involves: C57BL/6N)
|
abnormal autophagy
|
J:231818
|
Tmem203tm1.1Roml/Tmem203tm1.1Roml
(involves: C57BL/6)
|
abnormal endoplasmic reticulum physiology
|
J:222925
|
abnormal sperm head morphology
|
J:222925
|
azoospermia
|
J:222925
|
Tmem216em1Cya/Tmem216em1Cya
(involves: C57BL/6J)
|
abnormal cell cycle
|
J:345410
|
abnormal cilium morphology
|
J:345410
|
abnormal kidney epithelial cell primary cilium morphology
|
J:345410
|
decreased kidney epithelial cell primary cilium length
|
J:345410
|
Tmem219tm1(KOMP)Vlcg/Tmem219tm1(KOMP)Vlcg
(B6J.B6N-Tmem219tm1(KOMP)Vlcg)
|
increased lung apoptosis
|
J:236976
|
Tmem225em1Jliu/Tmem225em1Jliu
(C57BL/6-Tmem225em1Jliu)
|
abnormal mitochondrial physiology
|
J:345843
|
abnormal sperm flagellum morphology
|
J:345843
|
abnormal sperm midpiece morphology
|
J:345843
|
asthenozoospermia
|
J:345843
|
decreased cellular ATP level
|
J:345843
|
decreased sperm progressive motility
|
J:345843
|
hairpin sperm flagellum
|
J:345843
|
kinked sperm flagellum
|
J:345843
|
oxidative stress
|
J:345843
|
Tmem232em1Shliu/Tmem232em1Shliu
(C57BL/6-Tmem232em1Shliu)
|
abnormal outer dense fiber morphology
|
J:338029
|
abnormal sperm axoneme morphology
|
J:338029
|
abnormal sperm fibrous sheath morphology
|
J:338029
|
abnormal sperm flagellum morphology
|
J:338029
|
asthenozoospermia
|
J:338029
|
decreased sperm progressive motility
|
J:338029
|
hairpin sperm flagellum
|
J:338029
|
oligozoospermia
|
J:338029
|
Tmem249em1Osb/Tmem249em1Osb
(involves: C57BL/6 * DBA/2)
|
abnormal activated sperm motility
|
J:337426
|
asthenozoospermia
|
J:337426
|
decreased hyperactivated sperm motility
|
J:337426
|
decreased sperm progressive motility
|
J:337426
|
Tmem258tm1.1(KOMP)Vlcg/Tmem258+
(involves: C57BL/6NTac)
|
abnormal enterocyte proliferation
|
J:240635
|
increased endoplasmic reticulum stress
|
J:240635
|
increased enterocyte apoptosis
|
J:240635
|
Tmem268em1Cheyy/Tmem268em1Cheyy
(involves: C57BL/6)
|
abnormal leukocyte adhesion
|
J:350812
|
abnormal vesicle-mediated transport
|
J:350812
|
impaired leukocyte migration
|
J:350812
|
impaired macrophage phagocytosis
|
J:350812
|
impaired neutrophil phagocytosis
|
J:350812
|
Tmf1tm1Unir/Tmf1tm1Unir
(involves: 129/Sv * ICR)
|
abnormal sperm midpiece morphology
|
J:166798
|
abnormal sperm mitochondrial sheath morphology
|
J:166798
|
abnormal spermatid morphology
|
J:166798
|
absent acrosome
|
J:166798
|
asthenozoospermia
|
J:166798
|
globozoospermia
|
J:166798
|
tmgc42/tmgc42
(Mixed stock)
|
abnormal neuronal migration
|
J:92490
|
Tmigd3Tg(H2-K-CALR*)del52Shmd/0
(involves: C57BL/6 * DBA/2)
|
abnormal megakaryocyte differentiation
|
J:241724
|
Tmlheem1Plaa/Tmlheem1Plaa
(C57BL/6N-Tmlheem1Plaa)
|
abnormal mitochondrial physiology
|
J:341247
|
decreased fatty acid oxidation
|
J:341247
|
Tmod3Gt(RRF004)Byg/Tmod3Gt(RRF004)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle
|
J:208725
|
Tmpotm1.1Foi/Tmpotm1.1Foi
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell cycle
|
J:145628
|
abnormal enterocyte proliferation
|
J:145628
|
Tmprss3m1Ingm/Tmprss3m1Ingm
(C3HeB/FeJ-Tmprss3m1Ingm)
|
abnormal kinocilium morphology
|
J:172676
|
Tmprss6tm1Dgen/Tmprss6+
(B6.129P2-Tmprss6tm1Dgen/Crl)
|
maternal effect
|
J:160248
|
Tmprss12em1Huizh/Tmprss12em1Huizh
(C57BL/6-Tmprss12em1Huizh)
|
abnormal double-strand DNA break repair
|
J:324488
|
abnormal male meiosis
|
J:324488
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:324488
|
abnormal mitochondrial crista morphology
|
J:324488
|
abnormal sperm midpiece morphology
|
J:324488
|
abnormal sperm mitochondrial sheath morphology
|
J:324488
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:324488
|
asthenozoospermia
|
J:324488
|
decreased male germ cell number
|
J:324488
|
decreased sperm progressive motility
|
J:324488
|
increased male germ cell apoptosis
|
J:324488
|
oligozoospermia
|
J:324488
|
Tmprss12em4Osb/Tmprss12em4Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
asthenozoospermia
|
J:293874
|
impaired sperm migration in female genital tract
|
J:293874
|
Tmtc3Gt(JST185)Byg/Tmtc3Gt(JST185)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell differentiation
|
J:178869
|
Tmtc3Gt(JST185)Byg/Tmtc3Gt(JST185)Byg
(involves: 129P2/OlaHsd * A/J)
|
abnormal cell differentiation
|
J:178869
|
Tmtc4tm1(KOMP)Vlcg/Tmtc4tm1(KOMP)Vlcg
(involves: C57BL/6J * C57BL/6NTac)
|
abnormal endoplasmic reticulum physiology
|
J:268046
|
increased endoplasmic reticulum stress
|
J:268046
|
increased sensitivity to induced cell death
|
J:268046
|
Tmub1tm1(KOMP)Vlcg/Tmub1tm1(KOMP)Vlcg
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal apoptosis
|
J:284575
|
abnormal cell physiology
|
J:284575
|
abnormal mitochondrial physiology
|
J:284575
|
decreased sensitivity to induced cell death
|
J:284575
|
Tnftm1Gkl/Tnftm1Gkl
(involves: 129S/SvEv * C57BL/6)
|
decreased keratinocyte proliferation
|
J:56068
|
Tnftm1Gkl/Tnftm1Gkl
(B6;129S-Tnftm1Gkl/J)
|
oligozoospermia
|
J:143457
|
Tnftm1Gkl/Tnftm1Gkl Zfp36tm1Pjb/Zfp36tm1Pjb
(involves: 129S/SvEv * C57BL/6)
|
oxidative stress
|
J:214114
|
Tnftm1Ljo/Tnftm1Ljo
(B6.129S1-Tnftm1Ljo)
|
decreased apoptosis
|
J:127028
|
Tnftm2Gkl/Tnf+
(involves: 129S/SvEv * C57BL/6J)
|
increased apoptosis
|
J:108572
|
increased cell migration
|
J:264147
|
increased cell proliferation
|
J:264147
|
increased fibroblast cell migration
|
J:264147
|
increased fibroblast proliferation
|
J:264147
|
Tnftm2Gkl/Tnf+ Tnfrsf1btm1.1Gkl/Tnfrsf1btm1.1Gkl Tg(Col6a1-cre)1Gkl/0
(involves: 129S/SvEv * C57BL/6 * C57BL/6J * CBA)
|
abnormal cell adhesion
|
J:264147
|
abnormal cell physiology
|
J:264147
|
abnormal fibroblast physiology
|
J:264147
|
Tnftm2Gkl/Tnf+ Tnfrsf1btm1.2Gkl/Tnfrsf1btm1.2Gkl
(involves: 129S/SvEv * C57BL/6 * C57BL/6J)
|
abnormal cell adhesion
|
J:264147
|
abnormal cell physiology
|
J:264147
|
abnormal fibroblast physiology
|
J:264147
|
Tnfaip2tm1.1Ohno/Tnfaip2tm1.1Ohno
(C.Cg-Tnfaip2tm1.1Ohno)
|
increased podocyte apoptosis
|
J:343202
|
Tnfaip3tm1.1Gvl/Tnfaip3tm1.1Gvl Tg(Vil1-cre)997Gum/0
(B6.Cg-Tnfaip3tm1.1Gvl Tg(Vil1-cre)997Gum)
|
increased enterocyte apoptosis
|
J:163410
|
Tnfaip3tm2Ama/Tnfaip3tm2Ama Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell apoptosis
|
J:163917
|
increased B cell proliferation
|
J:163917
|
Tnfaip8Gt(IST13629C1)Tigm/Tnfaip8Gt(IST13629C1)Tigm
(involves: C57BL/6N)
|
increased enterocyte apoptosis
|
J:223320
|
Tnfaip8l2tm1Yhcn/Tnfaip8l2tm1Yhcn
(129S6/SvEvTac-Tnfaip8l2tm1Yhcn)
|
abnormal T cell apoptosis
|
J:139785
|
Tnfrsf1atm1Blt/Tnfrsf1atm1Blt
(involves: 129P2/OlaHsd)
|
increased sensitivity to induced cell death
|
J:210950
|
Tnfrsf1atm1Imx/Tnfrsf1atm1Imx
(C57BL/6-Tnfrsf1atm1Imx)
|
abnormal neuron proliferation
|
J:112713
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:78637
|
Tnfrsf1atm1Imx/Tnfrsf1atm1Imx
(involves: C57BL/6)
|
increased sensitivity to induced cell death
|
J:173568
|
Tnfrsf1atm1Imx/Tnfrsf1atm1Imx Tnfrsf1btm1Imx/Tnfrsf1btm1Imx
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:78637
|
increased susceptibility to neuronal excitotoxicity
|
J:33864
|
Tnfrsf1atm1Mak/Tnfrsf1atm1Mak
(involves: 129S2/SvPas)
|
increased sensitivity to induced cell death
|
J:210950
|
Tnfrsf1btm1Imx/Tnfrsf1btm1Imx
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased susceptibility to dopaminergic neuron neurotoxicity
|
J:78637
|
Tnfrsf1btm1Mwm/Tnfrsf1btm1Mwm
(B6.129S2-Tnfrsf1btm1Mwm/J)
|
decreased T cell proliferation
|
J:107039
|
Tnfrsf4tm1Nik/Tnfrsf4tm1Nik
(involves: 129S4/SvJae * C57BL/6)
|
decreased T cell proliferation
|
J:58979,
J:64552
|
Tnfrsf9tm1Byk/Tnfrsf9tm1Byk
(B6.Cg-Tnfrsf9tm1Byk)
|
increased T cell proliferation
|
J:83996
|
Tnfrsf9tm1Byk/Tnfrsf9tm1Byk
(C.Cg-Tnfrsf9tm1Byk)
|
increased splenocyte proliferation
|
J:83722
|
increased T cell proliferation
|
J:83996
|
Tnfrsf10btm1Wsed/Tnfrsf10btm1Wsed
(involves: 129P2/OlaHsd)
|
decreased cellular sensitivity to gamma-irradiation
|
J:96816
|
Tnfrsf11atm1.1Sral/Tnfrsf11a+
(B6.129P2(Cg)-Tnfrsf11atm1.1Sral)
|
abnormal osteoclast differentiation
|
J:312215
|
Tnfrsf11atm1.1Sral/Tnfrsf11atm1.1Sral
(B6.129P2(Cg)-Tnfrsf11atm1.1Sral)
|
abnormal osteoclast differentiation
|
J:312215
|
Tnfrsf11atm1Imx/Tnfrsf11atm1Imx
(involves: 129 * C57BL/6)
|
abnormal osteoclast differentiation
|
J:57899
|
Tnfrsf11btm1Khs/Tnfrsf11btm1Khs
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:111153,
J:48325
|
Tnfrsf13btm1Rjb/Tnfrsf13btm1Rjb
(involves: 129X1/SvJ * C57BL/6)
|
increased B cell proliferation
|
J:69474
|
Tnfrsf13btm1Vmd/Tnfrsf13btm1Vmd
(involves: C57BL/6)
|
increased B cell proliferation
|
J:70172
|
increased mesangial cell number
|
J:82331
|
Tnfrsf13cBcmd1/Tnfrsf13cBcmd1
(A/WySnJ)
|
decreased B cell proliferation
|
J:122315
|
decreased T cell proliferation
|
J:92334
|
Tnfrsf14tm1Kpf/Tnfrsf14tm1Kpf
(B6.129P2-Tnfrsf14tm1Kpf)
|
increased T cell proliferation
|
J:99456
|
Tnfrsf18tm1Ppp/Tnfrsf18tm1Ppp
(involves: 129/Sv * C57BL/6)
|
abnormal cell cycle
|
J:77393
|
increased T cell apoptosis
|
J:77393
|
increased T cell proliferation
|
J:77393
|
Tnfrsf21tm1Arte/Tnfrsf21tm1Arte
(involves: C57BL/6NTac)
|
abnormal oligodendrocyte apoptosis
|
J:205651
|
Tnfrsf21tm1Ddy/Tnfrsf21tm1Ddy
(involves: 129S1/Sv * 129X1/SvJ)
|
increased B cell proliferation
|
J:109341
|
increased T cell proliferation
|
J:70594
|
Tnfrsf21tm1Vmd/Tnfrsf21tm1Vmd
(involves: C57BL/6)
|
increased T cell proliferation
|
J:72761
|
Tnfrsf25tm1Mjo/Tnfrsf25tm1Mjo
(involves: 129P2/OlaHsd)
|
decreased T cell apoptosis
|
J:84536
|
Tnfsf4tm1Shr/Tnfsf4tm1Shr
(involves: 129S4/SvJae)
|
decreased T cell proliferation
|
J:59203
|
Tnfsf4tm1Sug/Tnfsf4tm1Sug
(B6.129S4-Tnfsf4tm1Sug)
|
decreased T cell proliferation
|
J:80214
|
Tnfsf11tles/Tnfsf11tles
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal osteoblast physiology
|
J:179743
|
Tnfsf13tm1Pod/Tnfsf13tm1Pod
(B6.Cg-Tnfsf13tm1Pod)
|
increased T cell proliferation
|
J:141374
|
Tnfsf13btm1Msc/Tnfsf13btm1Msc
(involves: 129S2/SvPas)
|
decreased T cell proliferation
|
J:92334
|
Tnfsf14tm1Ddy/Tnfsf14tm1Ddy
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased T cell proliferation
|
J:84366
|
Tnfsf14tm1Kpf/Tnfsf14tm1Kpf
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased splenocyte proliferation
|
J:77250
|
decreased T cell proliferation
|
J:77250
|
Tnfsf14tm1Kpf/Tnfsf14tm1Kpf
(B6.129P2-Tnfsf14tm1Kpf)
|
abnormal osteoclast differentiation
|
J:294030
|
Tnfsf15tm1Cdon/Tnfsf15tm1Cdon
(B6.129-Tnfsf15tm1Cdon)
|
abnormal dendritic cell differentiation
|
J:136280
|
Tniktm1Grnt/Tniktm1Grnt
(involves: 129P2/OlaHsd * 129S5/SvEvBrd)
|
abnormal neuron differentiation
|
J:190924
|
Tnip1tm1.1Ama/Tnip1tm1.1Ama
(involves: C57BL/6J)
|
increased fibroblast apoptosis
|
J:145539
|
increased hepatocyte apoptosis
|
J:145539
|
Tnip1tm1.1Pcoh/Tnip1tm1.1Pcoh
(involves: 129P2/OlaHsd * C57BL/6)
|
increased B cell proliferation
|
J:176826
|
increased fibroblast apoptosis
|
J:176826
|
Tnks2tm1.1Susm/Tnks2tm1.1Susm
(involves: 129S/SvEv * C57BL/6)
|
cellular phenotype
|
J:106917
|
Tnks2tm1.1Yjc/Tnks2tm1.1Yjc
(involves: 129S1/Sv)
|
cellular phenotype
|
J:106918,
J:137985
|
decreased adipocyte glucose uptake
|
J:137985
|
Tnks2tm1Susm/Tnks2tm1Susm
(involves: 129S/SvEv * C57BL/6)
|
cellular phenotype
|
J:106917
|
TnksGt(RRC239)Byg/TnksGt(RRC239)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
increased muscle cell glucose uptake
|
J:154388
|
Tnkstm1.1Yjc/Tnkstm1.1Yjc
(involves: 129S1/Sv * FVB/N)
|
cellular phenotype
|
J:137985
|
Tnnc1tm1.1Jrpi/Tnnc1+
(involves: 129S6/SvEvTac * C57BL/6)
|
cardiac interstitial fibrosis
|
J:274007
|
Tnnc1tm1.1Jrpi/Tnnc1tm1.1Jrpi
(involves: 129S6/SvEvTac * C57BL/6)
|
cardiac interstitial fibrosis
|
J:274007
|
Tnni2tm1Sgao/Tnni2+
(involves: 129 * ICR)
|
decreased osteoblast proliferation
|
J:228857
|
Tnni3tm1.1Jdp/Tnni3tm1.1Jdp
(involves: 129S6/SvEvTac * C57BL/6)
|
cardiac interstitial fibrosis
|
J:180606
|
Tnni3ktm1.1Tfo/Tnni3ktm1.1Tfo
(involves: C57BL/6)
|
abnormal cell proliferation
|
J:249318
|
Tnnt2tm2Mmto/Tnnt2+
(involves: 129S/SvEv * C57BL/6)
|
cardiac interstitial fibrosis
|
J:137784
|
Tnnt2tm2Mmto/Tnnt2tm2Mmto
(involves: 129S/SvEv * C57BL/6)
|
cardiac interstitial fibrosis
|
J:137784
|
Tnp1tm1Mlm/Tnp1tm1Mlm
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal sperm nucleus morphology
|
J:61941
|
abnormal spermatid morphology
|
J:61941
|
asthenozoospermia
|
J:61941
|
coiled sperm flagellum
|
J:61941
|
Tnp2tm1Mzh/Tnp2tm1Mzh
(involves: 129S/SvEv * 129S7/SvEvBrd)
|
abnormal outer dense fiber morphology
|
J:72107
|
abnormal sperm axoneme morphology
|
J:72107
|
abnormal sperm midpiece morphology
|
J:72107
|
abnormal sperm nucleus morphology
|
J:72107
|
asthenozoospermia
|
J:72107
|
teratozoospermia
|
J:72107
|
Tnp2tm1Wen/Tnp2tm1Wen
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal acrosome morphology
|
J:76986
|
abnormal sperm head morphology
|
J:76986
|
asthenozoospermia
|
J:76986
|
detached acrosome
|
J:76986
|
teratozoospermia
|
J:76986
|
Tnrc6aGt(XE786)Byg/Tnrc6aGt(XE786)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cell proliferation
|
J:182447
|
Tns1tm1Efu/Tns1tm1Efu
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell adhesion
|
J:39202
|
Tns3Gt(XK294)Byg/Tns3Gt(XK294)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell migration
|
J:96666
|
decreased chondrocyte proliferation
|
J:96666
|
Tob1tm1Tya/Tob1tm1Tya
(involves: 129S4/SvJae * C57BL/6)
|
abnormal osteoblast differentiation
|
J:66504
|
increased cell proliferation
|
J:66504
|
Tob2tm1Tya/Tob2tm1Tya
(involves: 129S4/SvJae * C57BL/6)
|
abnormal osteoclast differentiation
|
J:134287
|
Tomm7em1Yihc/Tomm7em1Yihc
(Not Specified)
|
oxidative stress
|
J:285108
|
Top1mttm1.1Hlzh/Top1mttm1.1Hlzh
(Not Specified)
|
abnormal autophagy
|
J:189886
|
abnormal cell physiology
|
J:189886
|
abnormal cellular glucose uptake
|
J:189886
|
abnormal cellular respiration
|
J:189886
|
abnormal mitochondrial morphology
|
J:189886
|
abnormal mitochondrial physiology
|
J:189886
|
abnormal redox activity
|
J:189886
|
decreased fibroblast proliferation
|
J:189886
|
increased mitochondrial number
|
J:189886
|
oxidative stress
|
J:189886
|
Top2btm2.1Jcw/Top2btm2.1Jcw
(involves: 129S4/SvJae * 129S6/SvEvTac)
|
impaired neuronal migration
|
J:94879
|
Top3atm1Jcw/Top3atm1Jcw
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal inner cell mass proliferation
|
J:45652
|
Top3btm1Jcw/Top3btm1Jcw
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal male meiosis
|
J:82397
|
aneuploidy
|
J:82397
|
Top6blem1Arte/Top6blem2Arte
(involves: C57BL/6NTac)
|
abnormal meiosis
|
J:229524
|
abnormal synaptonemal complex
|
J:229524
|
arrest of male meiosis
|
J:229524
|
azoospermia
|
J:229524
|
Top6blem2Arte/Top6blem2Arte
(involves: C57BL/6NTac)
|
abnormal meiosis
|
J:229524
|
abnormal synaptonemal complex
|
J:229524
|
arrest of male meiosis
|
J:229524
|
azoospermia
|
J:229524
|
Topaz1tm1Ics/Topaz1tm1Ics
(involves: C57BL/6J * C57BL/6N)
|
abnormal male germ cell apoptosis
|
J:226405
|
abnormal male germ cell morphology
|
J:226405
|
arrest of male meiosis
|
J:226405
|
azoospermia
|
J:226405
|
cellular phenotype
|
J:226405
|
Topbp1tm1.1Dsh/Topbp1tm1.1Dsh
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6)
|
abnormal cell cycle
|
J:170406
|
abnormal cell physiology
|
J:170406
|
Topbp1tm1.2Dsh/Topbp1tm1.2Dsh
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * C57BL/6J)
|
decreased cell proliferation
|
J:170406
|
increased embryonic tissue cell apoptosis
|
J:170406
|
ToporsGt(DTM034)Byg/Topors+
(involves: 129P2/OlaHsd * C57BL/6J)
|
cellular phenotype
|
J:325276
|
ToporsGt(DTM034)Byg/ToporsGt(DTM034)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal fibroblast physiology
|
J:325276
|
abnormal mitosis
|
J:325276
|
aneuploidy
|
J:325276
|
decreased fibroblast proliferation
|
J:325276
|
Tor1atm1Wtd/Tor1a+
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:107596
|
Tor1atm1Wtd/Tor1a+ Tor1aip1Gt(GST004691)Lex/Tor1aip1+
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:160544
|
Tor1atm1Wtd/Tor1atm1Wtd
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:107596
|
Tor1atm1Wtd/Tor1atm2Wtd
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:107596
|
Tor1atm2Wtd/Tor1a+
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:107596
|
Tor1atm2Wtd/Tor1atm2Wtd
(involves: 129S1/Sv)
|
abnormal cell nucleus morphology
|
J:107596,
J:185289
|
Tor1atm2Wtd/Tor1atm2Wtd
(D2.129S1-Tor1atm2Wtd)
|
abnormal cell nucleus morphology
|
J:185289
|
Tor1atm4.2Wtd/Tor1atm4.2Wtd
(involves: 129S/SvEv * 129S1/Sv * C57BL/6)
|
abnormal cell nucleus morphology
|
J:225567
|
Tor1aip1Gt(GST004691)Lex/Tor1aip1Gt(GST004691)Lex
(Not Specified)
|
abnormal cell nucleus morphology
|
J:160544
|
Tp(Y)1CtSxr-a/+
(involves: CBA * PCT)
|
absent germ cells
|
J:5252
|
arrest of male meiosis
|
J:5252
|
decreased primordial germ cell number
|
J:5252
|
Tpbgtm1Plst/Tpbgtm1Plst
(Not Specified)
|
abnormal cell differentiation
|
J:128085
|
abnormal cell migration
|
J:128085
|
Tpbgtm1Plst/Tpbgtm1Plst
(involves: C57BL/6)
|
abnormal cell migration
|
J:160174
|
Tpcn2em1Lwbch/Tpcn2+
(C57BL/6J-Tpcn2em1Lwbch)
|
abnormal lysosome physiology
|
J:332654
|
Tpcn2em1Lwbch/Tpcn2em1Lwbch
(C57BL/6J-Tpcn2em1Lwbch)
|
abnormal lysosome morphology
|
J:332654
|
abnormal lysosome physiology
|
J:332654
|
Tpgs1Gt(ROSA22)Sor/Tpgs1Gt(ROSA22)Sor
(involves: 129S/SvEv * C57BL/6)
|
abnormal sperm axoneme morphology
|
J:79292
|
absent sperm axonemal central pair
|
J:79292
|
absent sperm flagellum
|
J:79292
|
teratozoospermia
|
J:79292
|
Tph1tm1c(KOMP)Wtsi/Tph1tm1c(KOMP)Wtsi Tg(Ins2-cre)23Herr/0
(involves: 129S4/SvJae * C57BL/6J * CBA/J)
|
decreased pancreatic beta cell proliferation
|
J:284574
|
Tph1tm1Kry/Tph1tm1Kry Tg(Vil1-cre)20Syr/0
(involves: C57BL/6 * DBA/2)
|
increased osteoblast proliferation
|
J:146078
|
Tpp1tm1.1Plob/Tpp1tm1.1Plob
(B6.129S1-Tpp1tm1.1Plob)
|
abnormal lysosome physiology
|
J:136105
|
Tpp1tm1Plob/Tpp1tm1.1Plob
(B6.129S1-Tpp1tm1Plob/Tpp1tm1.1Plob)
|
abnormal lysosome physiology
|
J:136105
|
Tpp1tm1Plob/Tpp1tm1Plob
(involves: 129S1/Sv * C57BL/6)
|
abnormal lysosome physiology
|
J:94884
|
Tpp1tm1Plob/Tpp1tm1Plob
(B6.129S1-Tpp1tm1Plob)
|
abnormal lysosome morphology
|
J:136105
|
abnormal lysosome physiology
|
J:136105
|
Tpp2tm1.1Gnie/Tpp2tm1.1Gnie
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell cycle
|
J:133572
|
early cellular replicative senescence
|
J:133572
|
increased T cell apoptosis
|
J:133572
|
Tppp2em1Nju/Tppp2em1Nju
(Not Specified)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:279929
|
abnormal mitochondrial morphology
|
J:279929
|
asthenozoospermia
|
J:279929
|
increased male germ cell apoptosis
|
J:279929
|
oligozoospermia
|
J:279929
|
Tpsab1m1/Tpsab1m1
(involves: C57BL/6J)
|
abnormal mast cell differentiation
|
J:142880
|
Tpsab1m1/Tpsab1m1 Tpsb2tm1(cre)Adch/Tpsb2tm1(cre)Adch
(B6.Cg-Tpsb2tm1(cre)Adch Tpsab1m1)
|
abnormal mast cell differentiation
|
J:142880
|
Tpsb2tm1.1Mfg/Tpsb2tm1.1Mfg
(B6.129-Tpsb2tm1.1Mfg)
|
abnormal mast cell differentiation
|
J:142880
|
impaired neutrophil chemotaxis
|
J:142880
|
Tpst2grt/Tpst2grt
(involves: DW/JMuaf)
|
azoospermia
|
J:137590
|
Tpt1tm1.1Atel/Tpt1tm1.1Atel
(involves: C57BL/6)
|
decreased cell proliferation
|
J:150991
|
increased embryonic tissue cell apoptosis
|
J:150991
|
Tpt1tm1.1Yen/Tpt1tm1.1Yen
(involves: 129 * C57BL/6)
|
decreased embryonic epiblast cell proliferation
|
J:127458
|
increased embryonic epiblast cell apoptosis
|
J:127458
|
Tpt1tm1Kefu/Tpt1+
(either: 129S6/SvEvTac-Tpt1tm1Kefu or B6.129S6-Tpt1tm1Kefu)
|
increased sensitivity to induced cell death
|
J:148696
|
Tptetm1Osb/Tptetm1Osb
(involves: C57BL/6N)
|
abnormal sperm midpiece morphology
|
J:282803
|
asthenozoospermia
|
J:282803
|
Tpx2Gt(D028B03)1.1Wrst/Tpx2Gt(D028B03)1.1Wrst
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal cell nucleus morphology
|
J:184948
|
abnormal mitosis
|
J:184948
|
abnormal mitotic spindle assembly checkpoint
|
J:184948
|
decreased cell proliferation
|
J:184948
|
polyploidy
|
J:184948
|
Tpx2Gt(D028B03)Wrst/Tpx2+
(involves: 129S2/SvPas * C57BL/6J)
|
aneuploidy
|
J:184948
|
Tpx2Gt(D028B03)Wrst/Tpx2Gt(D028B03)Wrst
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal mitotic spindle morphology
|
J:184948
|
polyploidy
|
J:184948
|
Traddtm1.1Mak/Traddtm1.1Mak
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N))
|
decreased sensitivity to induced cell death
|
J:138824
|
Traf1tm1Tsi/Traf1tm1Tsi
(involves: 129S4/SvJae * C57BL/6)
|
increased sensitivity to induced cell death
|
J:72327
|
increased T cell proliferation
|
J:72327
|
Traf2tm1Mak/Traf2tm1Mak
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * BALB/c * C57BL/6J))
|
abnormal cell physiology
|
J:44360
|
increased sensitivity to induced cell death
|
J:44360
|
increased thymocyte apoptosis
|
J:44360
|
Traf3tm1Bshp/Traf3tm1Bshp Cd19tm1(cre)Cgn/Cd19+
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 * SJL)
|
decreased B cell apoptosis
|
J:124329
|
Traf3ip1Gt(RRJ005)Byg/Traf3ip1Gt(RRJ005)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
absent embryonic cilia
|
J:178483
|
Traf3ip2tm1.1Lix/Traf3ip2tm1.1Lix
(B6.129-Traf3ip2tm1.1Lix)
|
increased mesangial cell number
|
J:187766
|
Traf3ip2tm1Sbn/Traf3ip2tm1Sbn
(either: B6.129-Traf3ip2tm1Sbn or (involves: 129) or (involves: 129 * BALB/c))
|
impaired macrophage chemotaxis
|
J:144320
|
Traf4tm1Mrio/Traf4tm1Mrio
(involves: 129X1/SvJ)
|
abnormal cell migration
|
J:142780
|
Traf5tm1Hna/Traf5tm1Hna
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal B cell proliferation
|
J:57114
|
abnormal T cell proliferation
|
J:57114
|
Traf6tm1Jino/Traf6tm1Jino
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:77453
|
Traf6tm1Mak/Traf6tm1Mak
(involves: 129P3/J)
|
decreased B cell proliferation
|
J:54467
|
Traf6tm1Ywc/Traf6tm1Ywc
(Not Specified)
|
abnormal dendritic cell differentiation
|
J:85808
|
Traiptm1Jarh/Traiptm1Jarh
(involves: C57BL/6J)
|
decreased cell proliferation
|
J:127324
|
increased embryonic tissue cell apoptosis
|
J:127324
|
Trap1em1Iimcb/Trap1+
(B6.CBA-Trap1em1Iimcb/Tar)
|
abnormal neuron mitochondrial morphology
|
J:361875
|
Trap1em1Iimcb/Trap1em1Iimcb
(B6.CBA-Trap1em1Iimcb/Tar)
|
abnormal neuron mitochondrial morphology
|
J:361875
|
Trap1Gt(E150H04)Wrst/Trap1Gt(E150H04)Wrst
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal oxidative phosphorylation
|
J:226880
|
decreased fibroblast proliferation
|
J:226880
|
oxidative stress
|
J:226880
|
Trappc9tm1a(EUCOMM)Wtsi/Trappc9+
(involves: C57BL/6N)
|
paternal imprinting
|
J:294716
|
Trarg1tm1a(KOMP)Wtsi/Trarg1tm1a(KOMP)Wtsi
(C57BL/6N-Trarg1tm1a(KOMP)Wtsi)
|
decreased adipocyte glucose uptake
|
J:234039
|
Trem2em2Bwef/Trem2em2Bwef
(involves: C57BL/6J * DBA/2J * FVB/N)
|
decreased macrophage proliferation
|
J:242126
|
impaired macrophage phagocytosis
|
J:242126
|
increased macrophage apoptosis
|
J:242126
|
Trem2tm1(KOMP)Vlcg/Trem2tm1(KOMP)Vlcg
(C57BL/6N-Trem2tm1(KOMP)Vlcg)
|
abnormal cell cycle checkpoint function
|
J:239381
|
abnormal glial cell apoptosis
|
J:239381
|
Trex2tm1.2Coso/Y
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
|
decreased keratinocyte apoptosis
|
J:151766
|
Trex2tm1.2Coso/Trex2tm1.2Coso
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1)
|
decreased keratinocyte apoptosis
|
J:151766
|
Trib3Gt(OST324148)Lex/Trib3Gt(OST324148)Lex
(B6;129S5-Trib3Gt(OST324148)Lex/Ieg)
|
decreased pancreatic beta cell apoptosis
|
J:217758
|
Trib3tm1Tord/Trib3tm1Tord
(involves: C57BL/6)
|
decreased mast cell degranulation
|
J:192615
|
Trim9tm1.1Slgu/Trim9tm1.1Slgu
(involves: 129S4/SvJae * BALB/cJ * C57BL/6)
|
abnormal neuron differentiation
|
J:215804
|
Trim24tm1.1Los/Trim24tm1.1Los
(involves: 129/Sv * C57BL/6 * SJL)
|
increased hepatocyte proliferation
|
J:130210
|
polyploidy
|
J:130210
|
Trim27Gt(XP0484)Wtsi/Trim27Gt(XP0484)Wtsi
(B6.129P2-Trim27Gt(XP0484)Wtsi)
|
early cellular replicative senescence
|
J:189317
|
Trim27tm1Sis/Trim27tm1Sis
(B6.Cg-Trim27tm1Sis)
|
decreased hepatocyte apoptosis
|
J:206755
|
decreased sensitivity to induced cell death
|
J:206755
|
Trim28tm1.1Ipc/Trim28tm1.1Ipc Plekha5Tg(AMH-cre)1Flor/Plekha5+
(involves: 129S2/SvPas * C57BL/6 * SJL)
|
abnormal spermatid morphology
|
J:170392
|
decreased elongated spermatid number
|
J:170392
|
decreased male germ cell number
|
J:170392
|
oligozoospermia
|
J:170392
|
Trim28tm1Fca/Trim28tm1Fca
(Not Specified)
|
abnormal cell cycle
|
J:170392
|
Trim29tm1a(EUCOMM)Wtsi/Trim29tm1a(EUCOMM)Wtsi
(involves: C57BL/6N * C57BL/6NTac)
|
abnormal redox activity
|
J:349246
|
decreased endoplasmic reticulum stress
|
J:349246
|
decreased fetal cardiomyocyte apoptosis
|
J:349246
|
Trim29tm1c(EUCOMM)Wtsi/Trim29tm1c(EUCOMM)Wtsi Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6J * C57BL/6N * C57BL/6NTac)
|
decreased endoplasmic reticulum stress
|
J:349246
|
decreased fetal cardiomyocyte apoptosis
|
J:349246
|
increased T cell proliferation
|
J:349246
|
Trim30atm1Yjk/Trim30atm1Yjk
(B6.129P2-Trim30atm1Yjk)
|
increased T cell proliferation
|
J:215171
|
Trim36tm1Htan/Trim36tm1Htan
(involves: C57BL/6)
|
decreased sperm progressive motility
|
J:307617
|
Trim37Gt(RRO307)Byg/Trim37Gt(RRO307)Byg
(B6J.129P2-Trim37Gt(RRO307)Byg)
|
abnormal male germ cell morphology
|
J:232482
|
absent germ cells
|
J:232482
|
absent oocytes
|
J:232482
|
cellular phenotype
|
J:232482
|
decreased oocyte number
|
J:232482
|
Trim40em1Caox/Trim40em1Caox
(involves: C57BL/6J)
|
abnormal fibroblast physiology
|
J:255265
|
Trim41em1Osb/Trim41em1Osb
(involves: C57BL/6NJcl * DBA/2NJcl)
|
abnormal male meiosis
|
J:325726
|
increased male germ cell apoptosis
|
J:325726
|
oligozoospermia
|
J:325726
|
Trim41tm1Osb/Trim41tm1Osb
(involves: C57BL/6NJcl * C57BL/6NSlc * DBA/2NJcl)
|
abnormal male meiosis
|
J:325726
|
abnormal sperm flagellum morphology
|
J:325726
|
abnormal sperm head morphology
|
J:325726
|
asthenozoospermia
|
J:325726
|
increased male germ cell apoptosis
|
J:325726
|
oligozoospermia
|
J:325726
|
short sperm flagellum
|
J:325726
|
Trim54tm1Eno/Trim54tm1Eno
(B6.Cg-Trim54tm1Eno)
|
increased cardiomyocyte apoptosis
|
J:120068
|
Trim66em1Emr/Trim66em1Emr
(FVB/NCrl-Trim66em1Emr)
|
paternal effect
|
J:349240
|
Trim66em2Emr/Trim66em2Emr
(C57BL/6JCrl-Trim66em2Emr)
|
paternal effect
|
J:349240
|
Trim71em1Ktka/Trim71+
(Not Specified)
|
abnormal neuron proliferation
|
J:335575
|
Trim71em1Ktka/Trim71em1Ktka
(C57BL/6J-Trim71em1Ktka)
|
premature neuronal precursor differentiation
|
J:335575
|
Trim71tm1695Arte/Trim71tm1695Arte Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6J * C57BL/6NTac * SJL)
|
abnormal neuron proliferation
|
J:335575
|
Triotm1Mst/Triotm1Mst
(involves: 129S4/SvJae * BALB/c)
|
abnormal neuronal migration
|
J:65380
|
Trip6tm1.2Pher/Trip6tm1.2Pher
(B6.129P2-Trip6tm1.2Plou)
|
decreased brain ependyma motile cilium length
|
J:312425
|
decreased brain ependyma motile cilium number
|
J:312425
|
Trip10tm1Sejc/Trip10tm1Sejc
(involves: 129S1/Sv * 129X1/SvJ * ICR)
|
increased adipocyte glucose uptake
|
J:159952
|
Trip11Gt(AJ0490)Wtsi/Trip11Gt(AJ0490)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell morphology
|
J:142875
|
Trip11m1Mawa/Trip11m1Mawa
(C57BL/6J-Trip11m1Mawa)
|
abnormal cell physiology
|
J:163656
|
abnormal endoplasmic reticulum morphology
|
J:163656
|
Trip11tm1.1Psmi/Trip11tm1.2Psmi Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/? Tg(CAG-cre/Esr1*)5Amc/?
(involves: 129/Sv * C57BL/6 * SJL/J)
|
abnormal Golgi vesicle transport
|
J:253969
|
Trip11tm1.1Psmi/Trip11tm1.2Psmi Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/? Tg(Col2a1-cre)1Bhr/?
(involves: 129/Sv * C57BL/6 * SJL/J)
|
abnormal Golgi stack morphology
|
J:253969
|
Trip12tm1Wgu/Trip12tm1Wgu
(Not Specified)
|
increased sensitivity to induced cell death
|
J:199251
|
Trip13Gt(CH0621)Wtsi/Trip13Gt(CH0621)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal chiasmata formation
|
J:163309
|
abnormal chromosomal synapsis
|
J:163309
|
abnormal female meiosis
|
J:163309
|
abnormal synaptonemal complex
|
J:163309
|
arrest of male meiosis
|
J:163309
|
Trip13Gt(RRB047)Byg/Trip13Gt(RRB047)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal chiasmata formation
|
J:163309
|
abnormal chromosomal synapsis
|
J:163309
|
abnormal DNA repair
|
J:123677
|
abnormal double-strand DNA break repair
|
J:163309,
J:123677
|
abnormal female meiosis
|
J:163309,
J:123677
|
abnormal synaptonemal complex
|
J:163309
|
arrest of male meiosis
|
J:163309,
J:123677
|
decreased oocyte number
|
J:123677
|
immotile sperm
|
J:123677
|
Trmq3FVB/N/?
(involves: DBA/1J * FVB/N)
|
abnormal T cell proliferation
|
J:94347
|
Trp53tm1.1Awbr/Trp53tm1.1Awbr
(involves: C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:169434
|
decreased sensitivity to induced cell death
|
J:169434
|
decreased thymocyte apoptosis
|
J:173271
|
Trp53tm1.1Brn/Trp53+ Tg(KRT14-cre)8Brn/?
(involves: 129P2/OlaHsd * FVB/N * SKH1)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:121734
|
Trp53tm1.1Brn/Trp53tm1.1Brn Tg(KRT14-cre)8Brn/?
(involves: 129P2/OlaHsd * FVB/N * SKH1)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:121734
|
Trp53tm1.1Brn/Trp53tm3Tyj Tg(KRT14-cre)8Brn/?
(involves: 129P2/OlaHsd * 129S4/SvJae * FVB/N * SKH1)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:121734
|
Trp53tm1.1Dgj/Trp53tm1.1Dgj
(involves: SKH)
|
decreased cellular sensitivity to ionizing radiation
|
J:162466
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:162466
|
Trp53tm1.1Hwan/Trp53tm1.1Hwan
(involves: C57BL/6 * C57BL/6N)
|
increased cellular sensitivity to DNA damaging agents
|
J:265556
|
Trp53tm1.1Manf/Trp53tm1.1Manf
(Not Specified)
|
decreased hematopoietic stem cell proliferation
|
J:201153
|
Trp53tm1.1Manf/Trp53tm1.1Manf
(involves: C57BL/6J)
|
decreased hematopoietic stem cell proliferation
|
J:201153
|
Trp53tm1.1Thst/Trp53tm1.1Thst
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
abnormal cell physiology
|
J:198482
|
decreased cellular sensitivity to gamma-irradiation
|
J:198482
|
decreased thymocyte apoptosis
|
J:198482
|
Trp53tm1.1Tldo/Trp53tm1.1Tldo
(involves: 129S2/SvPas * BALB/c * C57BL/6)
|
decreased telomere length
|
J:199308
|
increased thymocyte apoptosis
|
J:199308
|
Trp53tm1.1Wgu/Trp53tm1.1Wgu
(involves: 129S6/SvEvTac * C57BL/6)
|
cellular phenotype
|
J:186159
|
decreased cellular sensitivity to gamma-irradiation
|
J:186159
|
decreased thymocyte apoptosis
|
J:186159
|
increased fibroblast proliferation
|
J:186159
|
Trp53tm1.2Awbr/Trp53tm1.2Awbr
(involves: C57BL/6)
|
abnormal cell cycle
|
J:173271
|
decreased cellular sensitivity to gamma-irradiation
|
J:173271
|
decreased thymocyte apoptosis
|
J:173271
|
increased cell proliferation
|
J:173271
|
increased splenocyte proliferation
|
J:173271
|
Trp53tm1Adv/Trp53+
(involves: 129S4/SvJae * C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:93328
|
Trp53tm1Adv/Trp53tm1Adv
(involves: 129S4/SvJae * C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:93328
|
Trp53tm1Att/Trp53tm1Att
(involves: 129S4/SvJae)
|
abnormal cell cycle
|
J:96433
|
abnormal cell cycle checkpoint function
|
J:96433
|
decreased cellular sensitivity to gamma-irradiation
|
J:173395
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:96433
|
Trp53tm1Att/Trp53tm1Att
(involves: 129S4/SvJae)
|
abnormal cell cycle
|
J:96433
|
abnormal cell death
|
J:96433
|
Trp53tm1Att/Trp53tm1Att Gt(ROSA)26Sortm1(cre/ERT2)Tyj/?
(involves: 129S4/SvJae)
|
decreased apoptosis
|
J:173395
|
Trp53tm1Brd/Trp53+
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased neuron apoptosis
|
J:66953
|
Trp53tm1Brd/Trp53tm1Brd
(involves: 129S7/SvEvBrd)
|
abnormal cell cycle
|
J:118244,
J:175018
|
abnormal cell cycle checkpoint function
|
J:78491,
J:126186
|
abnormal cell physiology
|
J:110650,
J:57882,
J:186159
|
abnormal chromosome number
|
J:57882
|
decreased apoptosis
|
J:118602
|
decreased cellular sensitivity to gamma-irradiation
|
J:78491,
J:126186
|
decreased cellular sensitivity to ionizing radiation
|
J:175018,
J:118602
|
decreased sensitivity to induced cell death
|
J:118244,
J:57882,
J:126186
|
decreased thymocyte apoptosis
|
J:186159
|
delayed cellular replicative senescence
|
J:175018,
J:186159
|
increased cell proliferation
|
J:110650,
J:118602
|
increased cellular glucose import
|
J:186159
|
increased fibroblast proliferation
|
J:175018,
J:57882,
J:186159
|
oxidative stress
|
J:186159
|
Trp53tm1Brd/Trp53tm1Brd
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:126497
|
decreased apoptosis
|
J:126497,
J:66953,
J:108183
|
decreased neuron apoptosis
|
J:66953
|
Trp53tm1Brd/Trp53tm1Brd Trp73tm2Mak/Trp73tm2Mak
(involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J)
|
decreased cellular sensitivity to gamma-irradiation
|
J:157905
|
decreased thymocyte apoptosis
|
J:157905
|
Trp53tm1Brd/Trp53tm8Xu
(involves: 129S7/SvEvBrd)
|
abnormal male germ cell apoptosis
|
J:170216
|
increased enterocyte apoptosis
|
J:170216
|
Trp53tm1Brn/Trp53tm1Brn
(involves: 129P2/OlaHsd)
|
abnormal cell death
|
J:117113
|
abnormal cell migration
|
J:175978
|
abnormal cell physiology
|
J:175978
|
cellular phenotype
|
J:117113
|
Trp53tm1Brn/Trp53tm2Tyj
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
abnormal cell physiology
|
J:175978
|
Trp53tm1Gev/Trp53tm1Gev
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:99305
|
Trp53tm1Glo/Trp53tm1Glo
(involves: 129S7/SvEvBrd * C57BL/6J)
|
decreased thymocyte apoptosis
|
J:172038
|
Trp53tm1Holl/Trp53tm1Holl
(involves: 129/Sv * 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:68918
|
Trp53tm1Holl/Trp53tm1Holl
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:126497
|
Trp53tm1Holl/Trp53tm7.1Xu
(involves: 129P2/OlaHsd)
|
decreased thymocyte apoptosis
|
J:160414
|
Trp53tm1Ldo/Trp53+
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell physiology
|
J:73757
|
Trp53tm1Mlh/Trp53tm1Mlh
(involves: 129P2/OlaHsd)
|
abnormal cell cycle
|
J:115104
|
cellular phenotype
|
J:115104
|
decreased enterocyte apoptosis
|
J:54082
|
Trp53tm1Sia/Trp53tm1Sia
(involves: C57BL/6 * CBA)
|
abnormal cell proliferation
|
J:36762
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:85569
|
increased sensitivity to induced cell death
|
J:85569
|
Trp53tm1Snj/Trp53tm1Snj
(involves: C57BL/6)
|
decreased cellular sensitivity to ionizing radiation
|
J:87687
|
Trp53tm1Thst/Trp53tm1Thst
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal cell physiology
|
J:198482
|
decreased cellular sensitivity to gamma-irradiation
|
J:198482
|
decreased thymocyte apoptosis
|
J:198482
|
oxidative stress
|
J:198482
|
Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas)
|
decreased cellular sensitivity to gamma-irradiation
|
J:259337
|
decreased thymocyte apoptosis
|
J:158953
|
increased fibroblast proliferation
|
J:95316
|
Trp53tm1Tyj/Trp53+
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
decreased thymocyte apoptosis
|
J:80311
|
Trp53tm1Tyj/Trp53tm1.1Dgk
(involves: 129S * 129X1/SvJ * C57BL/6)
|
delayed cellular replicative senescence
|
J:180576
|
increased cell proliferation
|
J:180576
|
Trp53tm1Tyj/Trp53tm1.1Umol
(involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac)
|
decreased cellular sensitivity to gamma-irradiation
|
J:228632
|
Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6)
|
abnormal apoptosis
|
J:87501
|
abnormal mitochondrial morphology
|
J:244082
|
aneuploidy
|
J:87501
|
decreased cell proliferation
|
J:170976
|
decreased cellular sensitivity to gamma-irradiation
|
J:95318
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:170976
|
increased fibroblast proliferation
|
J:95318
|
Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas)
|
abnormal cell cycle checkpoint function
|
J:126920,
J:77907
|
abnormal neuron differentiation
|
J:102702
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:77907
|
decreased splenocyte apoptosis
|
J:195018
|
decreased T cell apoptosis
|
J:109354
|
decreased thymocyte apoptosis
|
J:158953,
J:195018,
J:126920
|
increased fibroblast proliferation
|
J:77907
|
polyploidy
|
J:109354
|
Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * BALB/c)
|
increased cellular sensitivity to ionizing radiation
|
J:116176
|
Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * FVB/N)
|
decreased cellular sensitivity to ionizing radiation
|
J:114161
|
Trp53tm1Tyj/Trp53tm1Tyj
(involves: 129S2/SvPas * C57BL/6 * CBA)
|
decreased thymocyte apoptosis
|
J:80311
|
Trp53tm1Tyj/Trp53tm1Tyj Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129S2/SvPas * C57BL/6 * C57BL/6NCrj)
|
abnormal autophagy
|
J:183674
|
abnormal mitochondrial chromosome morphology
|
J:183674
|
abnormal mitochondrial physiology
|
J:183674
|
decreased cardiomyocyte apoptosis
|
J:183674
|
oxidative stress
|
J:183674
|
Trp53tm1Tyj/Trp53tm1Tyj Trp63tm1.1Elrf/Trp63tm1.1Elrf
(either: (involves: 129S2/SvPas * C57BL/6 * FVB/N) or (involves: 129S2/SvPas * 129S4/SvJae * 129S6/SvEvTac * C57BL/6))
|
early cellular replicative senescence
|
J:151638
|
Trp53tm1Tyj/Trp53tm1Tyj Xrcc2tm1Pmc/Xrcc2tm1Pmc
(involves: 129S1/Sv * 129S2/SvPas * C57BL/6)
|
decreased neuron apoptosis
|
J:111068
|
Trp53tm1Tyj/Trp53tm2.1Umol
(involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * C57BL/6NTac)
|
decreased cellular sensitivity to gamma-irradiation
|
J:228632
|
Trp53tm1Wahl/Trp53tm1Wahl
(involves: 129S4/SvJae)
|
abnormal cell cycle
|
J:64367,
J:100189
|
decreased cellular sensitivity to gamma-irradiation
|
J:64367
|
increased fibroblast proliferation
|
J:64367
|
Trp53tm1Wahl/Trp53tm1Wahl
(involves: C57BL/6)
|
decreased fibroblast apoptosis
|
J:108183
|
Trp53tm1Xu/Trp53tm1Xu
(involves: 129S4/SvJae)
|
abnormal thymocyte apoptosis
|
J:86185
|
decreased cellular sensitivity to ionizing radiation
|
J:86185
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:86185
|
Trp53tm1Xu/Trp53tm1Xu Xrcc4tm1Fwa/Xrcc4tm1Fwa
(involves: 129P2/OlaHsd * 129S4/SvJae)
|
abnormal apoptosis
|
J:109354
|
Trp53tm1Yjc/Trp53tm1Yjc
(B6.129S1-Trp53tm1Yjc)
|
decreased splenocyte apoptosis
|
J:195018
|
Trp53tm2.1Dgj/Trp53tm2.1Dgj
(involves: SKH)
|
increased cellular sensitivity to ionizing radiation
|
J:162466
|
increased cellular sensitivity to ultraviolet irradiation
|
J:162466
|
Trp53tm2.1Kasa/Trp53tm2.1Kasa
(involves: 129P2/OlaHsd * C57BL/6)
|
cellular phenotype
|
J:186335
|
Trp53tm2.1Snj/Trp53+
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:175018
|
decreased cellular sensitivity to ionizing radiation
|
J:175018
|
increased fibroblast proliferation
|
J:175018
|
Trp53tm2.1Snj/Trp53tm2.1Snj
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell cycle
|
J:175018
|
decreased cellular sensitivity to ionizing radiation
|
J:175018
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:175018
|
delayed cellular replicative senescence
|
J:175018
|
increased fibroblast proliferation
|
J:175018
|
Trp53tm2.1Tyj/Trp53+
(involves: 129S4/SvJae)
|
decreased cellular sensitivity to gamma-irradiation
|
J:95316
|
increased cell proliferation
|
J:95316
|
Trp53tm2.1Wgu/Trp53tm2.1Wgu
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal cell cycle
|
J:186159
|
cellular phenotype
|
J:186159
|
decreased thymocyte apoptosis
|
J:186159
|
delayed cellular replicative senescence
|
J:186159
|
increased fibroblast proliferation
|
J:186159
|
Trp53tm2Att/Trp53tm2Att
(either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6))
|
abnormal cell cycle
|
J:131856
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:131856
|
early cellular replicative senescence
|
J:131856
|
Trp53tm2Glo/Trp53tm2Glo
(involves: 129/Sv * C57BL/6)
|
abnormal apoptosis
|
J:87501
|
Trp53tm2Mok/Trp53+
(involves: 129S/SvEv * C57BL/6)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:106931
|
Trp53tm2Tyj/Trp53tm2Tyj
(involves: 129S4/SvJae)
|
early cellular replicative senescence
|
J:175978
|
Trp53tm2Xu/Trp53tm2Xu
(involves: 129S6/SvEvTac)
|
decreased T cell apoptosis
|
J:109354
|
decreased T cell proliferation
|
J:109354
|
Trp53tm3.1Glo/Trp53+
(B6.129S7-Trp53tm3.1Glo)
|
abnormal cell cycle
|
J:95318
|
decreased cellular sensitivity to gamma-irradiation
|
J:95318
|
increased fibroblast proliferation
|
J:95318
|
Trp53tm3.1Glo/Trp53tm3.1Glo
(B6.129S7-Trp53tm3.1Glo)
|
increased DNA replication
|
J:95318
|
increased fibroblast proliferation
|
J:95318
|
Trp53tm3.1Holl/Trp53tm3.1Holl
(Not Specified)
|
abnormal cell physiology
|
J:191183
|
increased thymocyte apoptosis
|
J:191183
|
Trp53tm3.1Tyj/Trp53+
(involves: 129S4/SvJae)
|
decreased cellular sensitivity to gamma-irradiation
|
J:95316
|
increased cell proliferation
|
J:95316
|
Trp53tm3Att/Trp53tm3Att
(involves: 129S4/SvJae)
|
cellular phenotype
|
J:173395
|
Trp53tm3Att/Trp53tm3Att Gt(ROSA)26Sortm1(cre/ERT2)Tyj/?
(involves: 129S4/SvJae)
|
cellular phenotype
|
J:173395
|
Trp53tm3Tyj/Trp53+ Tg(KRT14-cre)8Brn/?
(involves: 129S4/SvJae * FVB/N * SKH1)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:121734
|
Trp53tm3Tyj/Trp53tm3Tyj
(involves: 129S4/SvJae)
|
early cellular replicative senescence
|
J:175978
|
Trp53tm3Wahl/Trp53tm3Wahl
(involves: 129S4/SvJae)
|
abnormal cell cycle
|
J:118244,
J:108183
|
decreased apoptosis
|
J:118244,
J:108183
|
decreased cellular sensitivity to gamma-irradiation
|
J:118244
|
increased cell proliferation
|
J:108183
|
Trp53tm3Xu/Trp53tm3Xu
(Not Specified)
|
increased cellular sensitivity to ionizing radiation
|
J:112302
|
Trp53tm4Att/Trp53tm4Att
(involves: 129S4/SvJae)
|
decreased cellular sensitivity to gamma-irradiation
|
J:173395
|
Trp53tm4Att/Trp53tm4Att Gt(ROSA)26Sortm1(cre/ERT2)Tyj/?
(involves: 129S4/SvJae)
|
decreased apoptosis
|
J:173395
|
Trp53tm4Tyj/Trp53tm4Tyj
(involves: 129S4/SvJae * C57BL/6)
|
decreased cellular sensitivity to gamma-irradiation
|
J:92917
|
Trp53tm4Xu/Trp53+
(Not Specified)
|
cellular phenotype
|
J:160414
|
Trp53tm4Xu/Trp53tm4Xu
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:126497
|
decreased apoptosis
|
J:126497
|
spontaneous chromosome breakage
|
J:126497
|
Trp53tm5Tyj/Trp53tm5Tyj
(involves: 129S4/SvJae)
|
abnormal cell cycle
|
J:96433
|
abnormal cell death
|
J:118233,
J:96433
|
abnormal chromosome number
|
J:118233
|
Trp53tm5Tyj/Trp53tm5Tyj
(involves: 129S4/SvJae)
|
cellular phenotype
|
J:96433
|
Trp53tm5Wahl/Trp53tm5Wahl
(involves: 129S4/SvJae)
|
cellular phenotype
|
J:118244
|
Trp53tm5Xu/Trp53tm5Xu
(Not Specified)
|
decreased apoptosis
|
J:126497
|
spontaneous chromosome breakage
|
J:126497
|
Trp53tm6Wahl/Trp53tm6Wahl
(involves: 129S4/SvJae)
|
cellular phenotype
|
J:118244
|
Trp53tm7.1Xu/Trp53+
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:160414
|
chromosomal instability
|
J:160414
|
Trp53tm7.1Xu/Trp53tm7.1Xu
(Not Specified)
|
abnormal cell cycle checkpoint function
|
J:160414
|
chromosomal instability
|
J:160414
|
decreased thymocyte apoptosis
|
J:160414
|
Trp53bp1Gt(OST94324)Lex/Trp53bp1Gt(OST94324)Lex
(involves: 129S5/SvEvBrd)
|
chromosomal instability
|
J:83164
|
decreased cell proliferation
|
J:83164
|
induced chromosome breakage
|
J:83164
|
spontaneous chromosome breakage
|
J:83164
|
Trp53bp1tm1Jc/Trp53bp1tm1Jc
(involves: 129 * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:82512
|
aneuploidy
|
J:82512
|
chromosomal instability
|
J:82512
|
decreased cell proliferation
|
J:82512
|
increased cellular sensitivity to ionizing radiation
|
J:82512
|
Trp53bp1tm1Jc/Trp53bp1tm1Jc
(involves: 129)
|
abnormal cell physiology
|
J:194603
|
abnormal DNA repair
|
J:195061
|
abnormal double-strand DNA break repair
|
J:231089
|
increased cellular sensitivity to hydroxyurea
|
J:194603
|
increased cellular sensitivity to ionizing radiation
|
J:194603,
J:231089
|
Trp53bp2tm1Cdlo/Trp53bp2+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:146764
|
Trp53bp2tm1Xlu/Trp53bp2tm1Xlu
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal neuronal precursor proliferation
|
J:162396
|
increased neuron apoptosis
|
J:162396
|
Trp53bp2tm1Xlu/Trp53bp2tm1Xlu
(C.129S6-Trp53bp2tm1Xlu)
|
abnormal neuron differentiation
|
J:162396
|
abnormal neuronal migration
|
J:162396
|
Trp53inp1tm1Acar/Trp53inp1tm1Acar
(involves: 129/Sv * C57BL/6)
|
abnormal cell morphology
|
J:233434
|
abnormal mitochondrial morphology
|
J:233434
|
abnormal mitochondrial physiology
|
J:233434
|
abnormal mitophagy
|
J:233434
|
abnormal oxidative phosphorylation
|
J:233434
|
abnormal respiratory electron transport chain
|
J:233434
|
increased mitochondrial number
|
J:233434
|
oxidative stress
|
J:233434,
J:118867
|
Trp53inp2tm1Azo/Trp53inp2tm1Azo Myl1tm1(cre)Sjb/Myl1+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
impaired autophagy
|
J:212763
|
Trp53inp2tm1c(KOMP)Mbp/Trp53inp2tm1c(KOMP)Mbp Tg(Th-cre)#Gsat/0
(involves: 129S4/SvJaeSor * C57BL/6N * FVB/N)
|
abnormal axon extension
|
J:276249
|
Trp63tm1.1Elrf/Trp63tm1.1Elrf
(involves: C57BL/6 * FVB/N)
|
aneuploidy
|
J:151638
|
chromosomal instability
|
J:151638
|
early cellular replicative senescence
|
J:151638
|
Trp63tm1.1Elrf/Trp63tm1.1Elrf
(involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6)
|
aneuploidy
|
J:151638
|
chromosomal instability
|
J:151638
|
early cellular replicative senescence
|
J:151638
|
Trp63tm1Fmc/Trp63tm1Fmc
(involves: 129S4/SvJae)
|
decreased apoptosis
|
J:178316
|
increased apoptosis
|
J:54637
|
Trp63tm1Sin/Trp63tm1Sin
(Not Specified)
|
abnormal keratinocyte differentiation
|
J:181275
|
decreased keratinocyte proliferation
|
J:181275
|
Trp63tm2.1Aam/Trp63tm2.1Aam
(Not Specified)
|
abnormal cellular replicative senescence
|
J:158291
|
Trp63tm2Aam/Trp63tm2Aam
(Not Specified)
|
abnormal cellular replicative senescence
|
J:158291
|
Trp63tm2Brd/Trp63tm2Brd
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal mitochondrial physiology
|
J:119657
|
increased apoptosis
|
J:119657
|
Trp63tm2Brd/Trp63tm2Brd
(involves: 129S7/SvEvBrd)
|
decreased cell proliferation
|
J:100483
|
early cellular replicative senescence
|
J:100483
|
Trp63tm2Fmc/Trp63tm2Fmc
(involves: BALB/c)
|
decreased cellular sensitivity to ionizing radiation
|
J:116176
|
Trp63tm3.1Aam/Trp63+
(involves: 129S7/SvEvBrd * BALB/c * C57BL/6)
|
decreased keratinocyte proliferation
|
J:294158
|
Trp63tm3.1Brd/Trp63tm3.1Brd
(involves: 129S7/SvEvBrd)
|
decreased cell proliferation
|
J:100483
|
early cellular replicative senescence
|
J:100483
|
Trp63tm3Aam/Trp63+
(involves: 129S7/SvEvBrd)
|
decreased keratinocyte proliferation
|
J:294158
|
Trp73tm1(cre)Agof/Trp73tm1(cre)Agof
(involves: 129S1/Sv * 129X1/SvJ)
|
increased neuron apoptosis
|
J:153209
|
Trp73tm1Mak/Trp73tm1Mak
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal cell cycle
|
J:142848
|
abnormal chromosome number
|
J:142848
|
abnormal meiotic spindle morphology
|
J:142848
|
abnormal spindle assembly in female meiosis
|
J:142848
|
decreased oocyte number
|
J:142848
|
maternal effect
|
J:142848
|
polyploidy
|
J:142848
|
Trp73tm2Mak/Trp73tm2Mak
(either: B6.129P2-Trp73tm2Mak or (involves: 129P2/OlaHsd * C57BL/6J))
|
increased cellular sensitivity to gamma-irradiation
|
J:157905
|
increased sensitivity to induced cell death
|
J:157905
|
increased thymocyte apoptosis
|
J:157905
|
Trpc5tm1.1Lbi/Y
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
decreased susceptibility to neuronal excitotoxicity
|
J:194590
|
Trpc5tm1.1Lbi/Trpc5tm1.1Lbi
(involves: 129S6/SvEvTac * C57BL/6 * CBA)
|
decreased susceptibility to neuronal excitotoxicity
|
J:194590
|
Trpm2tm1.1Jych/Trpm2tm1.1Jych
(involves: FVB/N)
|
oxidative stress
|
J:196475
|
Trpm7tm1Agry/Trpm7tm1Agry
(involves: 129)
|
abnormal cell physiology
|
J:205665
|
Trpt1tm1Dron/Trpt1tm1Dron
(involves: 129P2/OlaHsd)
|
cellular phenotype
|
J:189412
|
Trpv1tm1Jul/Trpv1tm1Jul
(B6.129X1-Trpv1tm1Jul/J)
|
abnormal neuronal precursor proliferation
|
J:102006
|
Trpv2tm1Mijc/Trpv2tm1Mijc
(involves: 129S6/SvEvTac * C57BL/6)
|
impaired macrophage chemotaxis
|
J:158505
|
impaired macrophage phagocytosis
|
J:158505
|
Trpv5Hcalc1/Trpv5+
(involves: C3H/HeH * C57BL/6J)
|
increased renal tubule apoptosis
|
J:196612
|
Trpv5Hcalc1/Trpv5Hcalc1
(involves: C3H/HeH * C57BL/6J)
|
increased renal tubule apoptosis
|
J:196612
|
Ts(417)2Lws/0
(involves: C3H/HeSnJ * C57BL/6J * C57BL/6JEiJ * DBA/2J)
|
abnormal male germ cell morphology
|
J:117029
|
arrest of male meiosis
|
J:117029
|
decreased sperm progressive motility
|
J:117029
|
Ts(1016)232Dn/0
(involves: C3H/HeSnJ * C57BL/6JEiJ)
|
abnormal male germ cell morphology
|
J:117029
|
arrest of male meiosis
|
J:117029
|
decreased sperm progressive motility
|
J:117029
|
oligozoospermia
|
J:117029
|
Ts(1217)4Rk/0
(involves: AEJ/GnRk * C3H/He * C57BL/6J * DBA/2J)
|
abnormal male germ cell morphology
|
J:117029
|
arrest of male meiosis
|
J:117029
|
decreased sperm progressive motility
|
J:117029
|
oligozoospermia
|
J:117029
|
Ts(16C-tel)1Cje/0
(involves: C3H/HeSnJ * C57BL/6J * Rb(11.16)2H * Rb(16.17)32Lub)
|
oligozoospermia
|
J:117029
|
Ts(16C-tel)1Cje/0
(involves: C57BL/6J * Rb(11.16)2H * Rb(16.17)32Lub)
|
abnormal neuron differentiation
|
J:241597
|
Ts(1716)65Dn/0
(involves: C3H/HeSnJ * C57BL/6JEi * DBA/2J)
|
abnormal male germ cell morphology
|
J:117029
|
arrest of male meiosis
|
J:117029
|
decreased sperm progressive motility
|
J:117029
|
oligozoospermia
|
J:117029
|
Ts(1716)65Dn/0
(involves: BALB/c * C3H/He * C57BL/6JEiJ * DBA/2J)
|
asthenozoospermia
|
J:331897
|
oligozoospermia
|
J:331897
|
Ts(1716)66Yah/0
(involves: C3H/HeSnJ * C57BL/6JEiJ * DBA/2J)
|
asthenozoospermia
|
J:331897
|
oligozoospermia
|
J:331897
|
Tsc1tm1Chdl/Tsc1tm1Chdl
(B6NHsd.129P2-Tsc1tm1Chdl)
|
increased embryonic tissue cell apoptosis
|
J:170999
|
Tsc1tm1Djk/Tsc1tm1.1Djk Tg(Syn1-cre)671Jxm/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
abnormal neuron differentiation
|
J:121858
|
Tsc1tm1Djk/Tsc1tm1Djk Tg(GFAP-cre)8Gtm/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
increased neuron apoptosis
|
J:134889
|
Tsc2tm1Djk/Tsc2+
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal autophagy
|
J:217829
|
Tsc2tm1Djk/Tsc2+ Atg7tm1Tchi/Atg7tm1Tchi Tg(Camk2a-cre)T29-1Stl/0
(involves: 129S4/SvJae * BALB/c * C57BL * C57BL/6 * CBA/JNCrlj)
|
abnormal autophagy
|
J:217829
|
Tsc2tm1Djk/Tsc2+ Tg(CAG-EGFP/Map1lc3b)53Nmz/0
(involves: 129S4/SvJae * C57BL/6 * C57BL/6J * C57BL/6NCrlj * DBA/2)
|
abnormal autophagosome formation
|
J:217829
|
Tsc2tm2.2Djk/Tsc2tm2.2Djk
(involves: 129S4/SvJae * C57BL/6)
|
increased apoptosis
|
J:149326
|
Tsc22d3tm1.1Hum/Y Tg(Ddx4-cre)1Dcas/0
(involves: 129S1/SvImJ * C57BL/6N * FVB)
|
azoospermia
|
J:226675
|
Tsc22d3tm1.1Ric/Y
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal spermatogonia proliferation
|
J:179667
|
arrest of male meiosis
|
J:179667
|
azoospermia
|
J:179667
|
decreased male germ cell number
|
J:179667
|
decreased round spermatid number
|
J:179667
|
Tsc22d3tm1.2Hum/Y
(involves: 129S1/SvImJ)
|
arrest of male meiosis
|
J:226675
|
azoospermia
|
J:226675,
J:223992
|
increased male germ cell apoptosis
|
J:226675
|
Tsc22d3tm1Ric/Y Tg(Ddx4-cre)1Dcas/?
(involves: C57BL/6 * FVB)
|
abnormal spermatid morphology
|
J:179667
|
arrest of male meiosis
|
J:179667
|
azoospermia
|
J:179667
|
decreased male germ cell number
|
J:179667
|
Tsg101tm1Mak/Tsg101tm1Mak
(either: (involves: 129P2/OlaHsd * C57BL/6J) or (involves: 129P2/OlaHsd * CD-1))
|
absent inner cell mass proliferation
|
J:67553
|
decreased cell proliferation
|
J:67553
|
decreased mitotic index
|
J:67553
|
Tsga8em1Ohbo/Y
(C57BL/6-Tsga8em1Ohbo)
|
abnormal spermatid morphology
|
J:307409
|
azoospermia
|
J:307409
|
increased testis apoptosis
|
J:307409
|
Tsga8em2Ohbo/Tsga8em2Ohbo
(C57BL/6-Tsga8em2Ohbo)
|
abnormal spermatid morphology
|
J:307409
|
azoospermia
|
J:307409
|
increased testis apoptosis
|
J:307409
|
Tsga10em1Smoc/Tsga10+
(involves: C57BL/6J)
|
abnormal sperm motility
|
J:307710
|
abnormal spermatogonia morphology
|
J:307710
|
Tshrhyt-2J/Tshrhyt-2J
(B6;129P3-Tshrhyt-2J/GrsrJ)
|
maternal effect
|
J:213054
|
Tsix/Xisttm3Sado/Tsix+
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
abnormal DNA methylation
|
J:130425
|
Tsix/Xisttm3Sado/Xist+
(involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ)
|
abnormal DNA methylation
|
J:130425
|
Tsixtm1.1Awu/Tsix+ Tg(CAG-EGFP)50Osb/0 Gt(ROSA)26Sortm1(rtTA)Awu/Gt(ROSA)26Sortm1(rtTA)Awu
(involves: 129P2/OlaHsd * 129S4/SvJae * C3H/HeSlc * C57BL/6J * C57BL/6Slc)
|
abnormal DNA methylation
|
J:174672
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:174672
|
abnormal imprinting
|
J:174672
|
Tsixtm1Jtl/Tsixtm1Jtl
(involves: 129S4/SvJae)
|
cellular phenotype
|
J:57967
|
Tsixtm2Jtl/Y
(involves: 129 * M. m. castaneus)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:57967
|
abnormal imprinting
|
J:57967
|
Tsixtm2Jtl/Tsix+
(involves: 129 * M. m. castaneus)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:57967
|
abnormal imprinting
|
J:57967
|
Tsixtm3Jtl/Y
(involves: 129)
|
abnormal imprinting
|
J:117335
|
Tsixtm3Jtl/Tsix+
(involves: 129)
|
abnormal imprinting
|
J:117335
|
Tsksem1Osb/Tsksem1Osb
(involves: 129S2/SvPas * C57BL/6NSlc)
|
abnormal sperm head morphology
|
J:337844
|
abnormal sperm midpiece morphology
|
J:337844
|
abnormal sperm mitochondrial sheath morphology
|
J:337844
|
abnormal spermatid morphology
|
J:337844
|
asthenozoospermia
|
J:337844
|
decreased sperm progressive motility
|
J:337844
|
increased male germ cell apoptosis
|
J:337844
|
teratozoospermia
|
J:337844
|
tsl/tsl
(B6NTacTcu.CByJNarl-tsl)
|
abnormal vacuole morphology
|
J:275934
|
tsl/tsl
(CByJNarl(B6NTacTcu)-tsl)
|
abnormal vacuole morphology
|
J:275934
|
Tslrn1em1Cwr/Y
(C57BL/6J-Tslrn1em1Cwr)
|
oligozoospermia
|
J:245211
|
Tslrn1em2Cwr/Y
(C57BL/6J-Tslrn1em2Cwr)
|
oligozoospermia
|
J:245211
|
TsnGt(OST63223)Lex/TsnGt(OST63223)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
arrest of male meiosis
|
J:85466
|
decreased cell proliferation
|
J:85466
|
increased male germ cell apoptosis
|
J:85466
|
oligozoospermia
|
J:85466
|
TsnaxGt(S21-6D1)Sor/TsnaxGt(S21-6D1)Sor
(involves: 129S4/SvJaeSor)
|
abnormal DNA repair
|
J:313427
|
increased cellular sensitivity to ionizing radiation
|
J:313427
|
increased fibroblast apoptosis
|
J:313427
|
Tsnaxip1em1Osb/Tsnaxip1em1Osb
(involves: C57BL/6J * DBA/2J)
|
decreased hyperactivated sperm motility
|
J:340908
|
decreased sperm progressive motility
|
J:340908
|
Tspan32Gt(pMS-1)1Jmt/Tspan32Gt(pMS-1)1Jmt
(involves: 129S1/Sv)
|
increased T cell proliferation
|
J:78033
|
Tspotm1.1Guwu/Tspotm1.1Guwu
(involves: C57BL/6)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:219189
|
Tspyl2tm1Sich/Y
(involves: 129S/SvEv)
|
abnormal cell cycle checkpoint function
|
J:174549
|
cellular phenotype
|
J:174549
|
Tspyl2tm1Sich/Tspyl2tm1Sich
(involves: 129S/SvEv)
|
abnormal cell cycle checkpoint function
|
J:174549
|
cellular phenotype
|
J:174549
|
Tspyl5em1Yuya/Tspyl5em1Yuya
(C57BL/6-Tspyl5em1Yuya)
|
abnormal male germ cell physiology
|
J:350814
|
abnormal spermatogonia proliferation
|
J:350814
|
decreased spermatogonia number
|
J:350814
|
oligozoospermia
|
J:350814
|
Tssk3em1Amsa/Tssk3em1Amsa
(involves: C57BL/6J * DBA/2J)
|
abnormal outer dense fiber morphology
|
J:334491
|
abnormal sperm axoneme morphology
|
J:334491
|
abnormal sperm flagellum morphology
|
J:334491
|
abnormal sperm head morphology
|
J:334491
|
detached acrosome
|
J:334491
|
immotile sperm
|
J:334491
|
oligozoospermia
|
J:334491
|
teratozoospermia
|
J:334491
|
Tssk3em1Osb/Tssk3em1Osb
(involves: 129S5/SvEvBrd * C57BL/6 * C57BL/6J * DBA/2)
|
abnormal acrosome morphology
|
J:337565
|
abnormal male germ cell morphology
|
J:337565
|
abnormal male germ cell physiology
|
J:337565
|
abnormal manchette morphology
|
J:337565
|
abnormal sperm head morphology
|
J:337565
|
abnormal sperm midpiece morphology
|
J:337565
|
detached acrosome
|
J:337565
|
oligozoospermia
|
J:337565
|
teratozoospermia
|
J:337565
|
Tssk3em2Amsa/Tssk3em2Amsa
(involves: C57BL/6J * DBA/2J)
|
immotile sperm
|
J:334491
|
oligozoospermia
|
J:334491
|
teratozoospermia
|
J:334491
|
Tssk3em3Amsa/Tssk3em3Amsa
(involves: C57BL/6J * DBA/2J)
|
immotile sperm
|
J:334491
|
oligozoospermia
|
J:334491
|
teratozoospermia
|
J:334491
|
Tssk4tm1.1Lgyu/Tssk4tm1.1Lgyu
(B6.129(129S2)-Tssk4tm1.1Lgyu)
|
abnormal sperm axoneme morphology
|
J:263443
|
abnormal sperm midpiece morphology
|
J:263443
|
abnormal sperm principal piece morphology
|
J:263443
|
decreased activated sperm motility
|
J:263443
|
Tssk6tm1Grj/Tssk6+
(involves: 129 * C57BL/6)
|
oligozoospermia
|
J:98891
|
Tssk6tm1Grj/Tssk6tm1Grj
(involves: 129 * C57BL/6)
|
abnormal sperm head morphology
|
J:98891
|
asthenozoospermia
|
J:98891
|
oligozoospermia
|
J:98891
|
Ttbk2bby/Ttbk2bby
(involves: C57BL/6J * FVB)
|
abnormal cilium morphology
|
J:197579
|
Ttbk2bby/Ttbk2tm1a(EUCOMM)Hmgu
(involves: C57BL/6 * C57BL/6N)
|
abnormal cilium morphology
|
J:269515
|
Ttbk2bby/Ttbk2tm1Dral
(involves: C57BL/6)
|
absent embryonic cilia
|
J:269515
|
Ttbk2tm1a(EUCOMM)Hmgu/Ttbk2tm1a(EUCOMM)Hmgu
(involves: C57BL/6 * C57BL/6N)
|
abnormal cilium morphology
|
J:269515
|
Ttbk2tm1Dral/Ttbk2tm1a(EUCOMM)Hmgu
(involves: C57BL/6 * C57BL/6N)
|
abnormal cilium morphology
|
J:269515
|
Ttbk2tm1Dral/Ttbk2tm1Dral
(involves: C57BL/6)
|
abnormal cell physiology
|
J:269515
|
absent embryonic cilia
|
J:269515
|
Ttc6em1Cya/Ttc6em1Cya
(C57BL/6J-Ttc6em1Cya)
|
abnormal sperm flagellum morphology
|
J:341550
|
decreased sperm progressive motility
|
J:341550
|
hairpin sperm flagellum
|
J:341550
|
Ttc8tm1Reed/Ttc8tm1Reed
(involves: 129)
|
abnormal olfactory epithelium cilium morphology
|
J:173465
|
Ttc21aem1Fzh/Ttc21aem1Fzh
(involves: C57BL/6)
|
abnormal sperm annulus morphology
|
J:279926
|
abnormal sperm axoneme morphology
|
J:279926
|
abnormal sperm connecting piece morphology
|
J:279926
|
abnormal sperm end piece morphology
|
J:279926
|
abnormal sperm flagellum morphology
|
J:279926
|
abnormal sperm midpiece morphology
|
J:279926
|
abnormal sperm principal piece morphology
|
J:279926
|
absent sperm axonemal central pair
|
J:279926
|
asthenozoospermia
|
J:279926
|
coiled sperm flagellum
|
J:279926
|
decreased sperm progressive motility
|
J:279926
|
detached sperm flagellum
|
J:279926
|
kinked sperm flagellum
|
J:279926
|
short sperm flagellum
|
J:279926
|
teratozoospermia
|
J:279926
|
Ttc21btm2c(KOMP)Wtsi/Ttc21baln Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129X1/SvJ * A/J * C57BL/6N)
|
decreased kidney epithelial cell primary cilium length
|
J:213263
|
increased kidney cell proliferation
|
J:213263
|
Ttc29em1Fzh/Ttc29em1Fzh
(involves: C57BL/6)
|
abnormal sperm end piece morphology
|
J:283265
|
abnormal sperm midpiece morphology
|
J:283265
|
abnormal sperm principal piece morphology
|
J:283265
|
asthenozoospermia
|
J:283265
|
decreased sperm progressive motility
|
J:283265
|
hairpin sperm flagellum
|
J:283265
|
Ttltm1Wehl/Ttltm1Wehl
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c))
|
abnormal neuron differentiation
|
J:99877
|
Ttll1Gt(OST372941)Lex/Ttll1Gt(OST372941)Lex
(involves: 129S5/SvEvBrd * C57BL/6)
|
abnormal sperm midpiece morphology
|
J:186050
|
absent sperm flagellum
|
J:186050
|
absent sperm head
|
J:186050
|
detached sperm flagellum
|
J:186050
|
immotile sperm
|
J:186050
|
oligozoospermia
|
J:186050
|
teratozoospermia
|
J:186050
|
Ttll1tm1Seto/Ttll1tm1Seto
(involves: 129S/SvEv * C57BL/6)
|
abnormal respiratory motile cilium morphology
|
J:161297
|
abnormal respiratory motile cilium physiology
|
J:161297
|
short sperm flagellum
|
J:161297
|
Ttll3tm1.2Ics/Ttll3tm1.2Ics Ttll8tm1.2Ics/Ttll8tm1.2Ics
(B6.129S2-Ttll3tm1.2Ics Ttll8tm1.2Ics)
|
asthenozoospermia
|
J:300009
|
decreased sperm progressive motility
|
J:300009
|
kinked sperm flagellum
|
J:300009
|
Ttll3tm1d(EUCOMM)Wtsi/Ttll3tm1d(EUCOMM)Wtsi
(involves: C57BL/6N)
|
abnormal photoreceptor connecting cilium morphology
|
J:249732
|
Ttll5tm1.1N/Ttll5tm1.1N
(involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N)
|
abnormal cell physiology
|
J:198583
|
abnormal sperm axoneme morphology
|
J:198583
|
asthenozoospermia
|
J:198583
|
coiled sperm flagellum
|
J:198583
|
teratozoospermia
|
J:198583
|
Ttll9tm1Seto/Ttll9tm1Seto
(involves: C57BL/6N)
|
abnormal sperm axoneme morphology
|
J:246509
|
abnormal sperm fibrous sheath morphology
|
J:246509
|
abnormal sperm principal piece morphology
|
J:246509
|
asthenozoospermia
|
J:246509
|
decreased sperm progressive motility
|
J:246509
|
detached sperm flagellum
|
J:246509
|
oligozoospermia
|
J:246509
|
teratozoospermia
|
J:246509
|
Ttnshru/Ttnshru
(B6.BTBR-Ttnshru)
|
cellular necrosis
|
J:92178
|
increased apoptosis
|
J:74786
|
Ttntm1.1Her/Ttntm1.1Her
(involves: 129S4/SvJae * 129T2/SvEms)
|
increased embryonic tissue cell apoptosis
|
J:111284
|
Ttntm1.1Isrd/Ttntm1.1Isrd
(involves: 129S2/SvPas * C57BL/6)
|
cardiac interstitial fibrosis
|
J:165576
|
Ttntm1Brge/Ttn+
(B6.Cg-Ttntm1Brge)
|
cardiac interstitial fibrosis
|
J:152736
|
Ttyh1tm1Tohe/Ttyh1tm1Tohe
(involves: C57BL/6 * C57BL/6J * CBA)
|
abnormal cell nucleus morphology
|
J:161796
|
abnormal mitosis
|
J:161796
|
increased cell nucleus count
|
J:161796
|
Tubtm1Rok/Tubtm1Rok
(C57BL/6-Tubtm1Rok)
|
increased retina apoptosis
|
J:59994
|
Tuba1aem1Rstot/Tuba1aem1Rstot
(involves: C57BL/6J * C57BL/6N)
|
increased neuronal precursor proliferation
|
J:278765
|
Tuba1aJna/Tuba1a+
(involves: BALB/cAnN * C3H/HeH)
|
impaired neuronal migration
|
J:117881
|
Tuba1aquas/Tuba1aquas
(involves: C57BL/6J)
|
abnormal neuronal migration
|
J:278765
|
decreased neuronal precursor proliferation
|
J:278765
|
increased neuron apoptosis
|
J:278765
|
increased neuronal precursor proliferation
|
J:278765
|
Tuba4am1Frla/Tuba4am1Frla
(BALB/c-Tuba4am1Frla)
|
abnormal megakaryocyte differentiation
|
J:286522
|
Tubb2bbrdp/Tubb2bbrdp
(involves: A/J * FVB)
|
abnormal neuronal precursor proliferation
|
J:201099
|
increased neuron apoptosis
|
J:201099
|
Tubb3tm1.1Ece/Tubb3tm1.1Ece
(involves: 129S/SvEv * C57BL/6J)
|
abnormal axon guidance
|
J:158992
|
Tubb4aJit/Tubb4aJit
(FVB.B6-Tubb4aJit)
|
increased neuron apoptosis
|
J:321692
|
Tubb4atm1(KOMP)Wtsi/Tubb4atm1(KOMP)Wtsi Tubb4btm2b(EUCOMM)Wtsi/Tubb4btm2b(EUCOMM)Wtsi
(involves: C57BL/6 * FVB)
|
abnormal respiratory motile cilium morphology
|
J:344732
|
Tubb4btm2b(EUCOMM)Wtsi/Tubb4btm2b(EUCOMM)Wtsi
(involves: C57BL/6 * FVB)
|
abnormal oviduct epithelium motile cilium morphology
|
J:344732
|
abnormal respiratory motile cilium morphology
|
J:344732
|
Tubb5tm1.1Dak/Tubb5tm1.1Dak Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal mitosis
|
J:240157
|
abnormal mitotic spindle morphology
|
J:240157
|
increased neuron apoptosis
|
J:240157
|
Tubb5tm2.1Dak/Tubb5+ Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
increased neuron apoptosis
|
J:240157
|
Tubb5tm2.1Dak/Tubb5tm2.1Dak Tg(Nes-cre)1Kln/0
(involves: 129P2/OlaHsd * C57BL/6 * SJL)
|
abnormal mitosis
|
J:240157
|
Tubg1tm1Sts/Tubg1tm1Sts
(involves: 129S4/SvJae * C57BL/6J)
|
abnormal mitotic spindle morphology
|
J:99398
|
Tubgcp4tm1Rzh/Tubgcp4+
(involves: 129S6/SvEv * C57BL/6)
|
enhanced autophagy
|
J:282705
|
Tubgcp4tm1Rzh/Tubgcp4tm1Rzh
(involves: 129S6/SvEv * C57BL/6)
|
decreased cell proliferation
|
J:282705
|
Tuft1tm1a(KOMP)Wtsi/Tuft1tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal keratinocyte differentiation
|
J:340887
|
decreased keratinocyte adhesion
|
J:340887
|
Tulp1tm1Pjn/Tulp1tm1Pjn
(involves: 129X1/SvJ * C57BL/6)
|
increased retina apoptosis
|
J:59884
|
Tulp2em1Huizh/Tulp2em1Huizh
(C57BL/6-Tulp2em1Huizh)
|
abnormal mitochondrial crista morphology
|
J:307539
|
abnormal sperm axoneme morphology
|
J:307539
|
abnormal sperm midpiece morphology
|
J:307539
|
abnormal spermatid morphology
|
J:307539
|
asthenozoospermia
|
J:307539
|
decreased sperm progressive motility
|
J:307539
|
increased testis apoptosis
|
J:307539
|
kinked sperm flagellum
|
J:307539
|
oligozoospermia
|
J:307539
|
Tulp2em1Zfhu/Tulp2em1Zfhu
(C57BL/6J-Tulp2em1Zfhu)
|
abnormal outer dense fiber morphology
|
J:357849
|
abnormal sperm axoneme morphology
|
J:357849
|
abnormal sperm flagellum morphology
|
J:357849
|
asthenozoospermia
|
J:357849
|
oligozoospermia
|
J:357849
|
teratozoospermia
|
J:357849
|
Tulp3m1Kflj/Tulp3m1Kflj
(involves: C57BL/6J * FVB/NJ)
|
increased kidney cell proliferation
|
J:284006
|
Tulp3tm1Jng/Tulp3+
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
increased embryonic neuroepithelium apoptosis
|
J:70060
|
Tulp3tm1Jng/Tulp3tm1Jng
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
increased apoptosis
|
J:70060
|
increased embryonic neuroepithelium apoptosis
|
J:70060
|
Tusc2tm1Avi/Tusc2tm1Avi
(involves: 129S1/Sv)
|
abnormal oxidative phosphorylation
|
J:309768
|
asthenozoospermia
|
J:309768
|
decreased T cell proliferation
|
J:309768
|
oligozoospermia
|
J:309768
|
Tut4Gt(RRR277)Byg/Tut4Gt(RRR277)Byg
(B6.129P2-Tut4Gt(RRR277)Byg)
|
abnormal cell physiology
|
J:194669
|
Tut4tm2.1Doca/Tut4tm2.1Doca Tut7tm2.1Doca/Tut7tm2.1Doca Tg(Zp3-cre)93Knw/0
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
abnormal female meiosis I arrest
|
J:262343
|
abnormal spindle assembly in female meiosis
|
J:262343
|
Tut4tm2.1Doca/Tut4tm3.1Doca Tut7tm2.1Doca/Tut7tm2.1Doca Tg(Zp3-cre)93Knw/0
(involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6J)
|
abnormal female meiosis I arrest
|
J:262343
|
abnormal spindle assembly in female meiosis
|
J:262343
|
Tvp23bem3Eetr/Tvp23bem3Eetr
(C57BL/6J-Tvp23bem3Eetr)
|
abnormal intestinal goblet cell physiology
|
J:340685
|
decreased colon goblet cell number
|
J:340685
|
Twist1Ska10/Twist1Ska10
(C57BL/6J-Twist1Ska10)
|
abnormal osteoblast differentiation
|
J:90056
|
Twist1tm1Bhr/Twist1+
(involves: 129S/Sv * 129X1/SvJ * C57BL/6)
|
abnormal osteoblast differentiation
|
J:90056
|
Twist2tm1(cre)Dor/Twist2+ Wnt7btm1Parr/Wnt7btm2Amc
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal osteoblast differentiation
|
J:117333
|
Twist2tm1(cre)Dor/Twist2tm1(cre)Dor
(involves: 129/Sv * 129X1/SvJ)
|
abnormal osteoblast differentiation
|
J:90056
|
Twnktm1.1Lrsn/Twnktm1.1Lrsn Tg(Ckmm-cre)5Khn/0
(involves: C57BL/6 * FVB)
|
abnormal mitochondrial morphology
|
J:194965
|
abnormal respiratory electron transport chain
|
J:194965
|
Twsg1tm1Nosa/Twsg1tm1Nosa
(involves: 129P2/OlaHsd * C57BL/6)
|
increased thymocyte apoptosis
|
J:82738
|
Txn1tm1Mmt/Txn1tm1Mmt
(involves: 129S2/SvPas * C57BL/6)
|
absent inner cell mass proliferation
|
J:35059
|
Txn2Gt(OST69169)Lex/Txn2Gt(OST69169)Lex
(involves: 129S5/SvEvBrd)
|
abnormal cellular respiration
|
J:81638
|
increased embryonic tissue cell apoptosis
|
J:81638
|
Txniptm1.1Rlee/Txniptm1.1Rlee
(involves: 129S4/SvJae)
|
increased cardiac muscle cell glucose uptake
|
J:141487
|
Txniptm1.1Road/Txniptm1.1Road
(B6.Cg-Txniptm1.1Road)
|
abnormal cellular respiration
|
J:132756
|
decreased cellular glucose uptake
|
J:132756
|
increased skeletal muscle cell glucose uptake
|
J:132756
|
Txniptm1Rlee/Txniptm1Rlee A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
(involves: 129S4/SvJae * FVB/N)
|
increased cardiac muscle cell glucose uptake
|
J:141487
|
Txniptm1Yu/Txniptm1Yu
(involves: 129)
|
increased T cell proliferation
|
J:96677
|
Txnrd1tm1.1Marc/Txnrd1tm1.1Marc
(involves: 129P2/OlaHsd * C57BL/6J)
|
absent fibroblast proliferation
|
J:96818
|
decreased cell proliferation
|
J:96818
|
Txnrd2tm1.1Marc/Txnrd2tm1.1Marc
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased fetal cardiomyocyte proliferation
|
J:94136
|
decreased fibroblast proliferation
|
J:94136
|
Txnrd3tm1Vgla/Txnrd3tm1Vgla
(Not Specified)
|
asthenozoospermia
|
J:330784
|
oligozoospermia
|
J:330784
|
Tyk2tm1Shmd/Tyk2tm1Shmd
(involves: 129P2/OlaHsd)
|
abnormal cell cycle
|
J:109408
|
Tyk2tm1Shmd/Tyk2tm1Shmd
(either: (involves: 129 * 129P2/OlaHsd) or (involves: 129P2/OlaHsd * C57BL/6))
|
abnormal fat cell differentiation
|
J:195099
|
abnormal mitochondrial physiology
|
J:195099
|
disorganized mitochondrial cristae
|
J:195099
|
Tymptm1Mihi/Tymptm1Mihi Upp1tm1Gp/Upp1tm1Gp
(involves: 129 * 129X1/SvJ * C57BL/6J)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:144245
|
abnormal mitochondrial morphology
|
J:144245
|
Tyrc-2J/Tyrc-2J
(B6(Cg)-Tyrc-2J/J)
|
abnormal keratinocyte apoptosis
|
J:112959
|
increased cellular sensitivity to ionizing radiation
|
J:112959
|
Tyrc-25H/Tyr+
(involves: AKR * STOCK Tyrc-25H/Tyrc-ch)
|
abnormal chromosome morphology
|
J:5520
|
induced chromosome breakage
|
J:5520
|
Tyrc-25H/Tyr+
(involves: SM/J * STOCK Tyrc-h/Tyrc-25H)
|
chromosome breakage
|
J:5437
|
induced chromosome breakage
|
J:5437
|
Tyrc-25H/Tyrc-25H
(involves: 101/H * AKR * C3H/H)
|
abnormal cell morphology
|
J:6256
|
abnormal cell nucleus morphology
|
J:6256
|
Tyrobptm1Lll/Tyrobptm1Lll
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal osteoclast differentiation
|
J:89583
|
decreased T cell proliferation
|
J:64763
|
Tyrobptm1Ttk/Tyrobptm1Ttk
(B6.129P2-Tyrobptm1Ttk)
|
increased B cell proliferation
|
J:177613
|
Tysnd1tm1.1Arte/Tysnd1tm1.1Arte
(involves: C57BL/6J * C57BL/6N)
|
abnormal acrosome morphology
|
J:223054
|
abnormal sperm axoneme morphology
|
J:223054
|
abnormal sperm mitochondrial sheath morphology
|
J:223054
|
globozoospermia
|
J:223054
|
Uacatm1Kiy/Uacatm1Kiy
(involves: 129P2/OlaHsd)
|
abnormal apoptosis
|
J:89918
|
Uba3tm1Tchi/Uba3tm1Tchi
(involves: C57BL/6 * CBA)
|
abnormal cell cycle
|
J:72808
|
abnormal inner cell mass apoptosis
|
J:72808
|
Uba7tm1Dez/Uba7tm1Dez Usp18tm1Dez/Usp18tm1Dez
(involves: 129 * C57BL/6)
|
increased sensitivity to induced cell death
|
J:144149
|
Ubap1em1Yta/Ubap1+
(involves: C57BL/6 * C57BL/6N * DBA/2)
|
impaired autophagy
|
J:332139
|
Ubash3btm1Jni/Ubash3btm1Jni Ubash3atm1Jni/Ubash3atm1Jni
(Not Specified)
|
increased T cell proliferation
|
J:89761
|
Ubbtm1Rrk/Ubbtm1Rrk
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
abnormal female meiosis
|
J:130361
|
abnormal oocyte morphology
|
J:130361
|
arrest of male meiosis
|
J:130361
|
decreased male germ cell number
|
J:130361
|
decreased oocyte number
|
J:130361
|
impaired spindle assembly in female meiosis
|
J:130361
|
thin zona pellucida
|
J:130361
|
Ubctm1Rrk/Ubctm1Rrk
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6J)
|
abnormal cell cycle
|
J:122574
|
abnormal cell death
|
J:122574
|
decreased cell proliferation
|
J:122574
|
early cellular replicative senescence
|
J:122574
|
Ubdtm1Smwe/Ubdtm1Smwe
(B6.129S6-Ubdtm1Smwe)
|
increased apoptosis
|
J:110321
|
Ube2btm1Jhjh/Ube2btm1Jhjh
(either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB/N))
|
abnormal chiasmata formation
|
J:81811
|
abnormal male meiosis
|
J:81811
|
abnormal spermatocyte morphology
|
J:81811
|
abnormal synaptonemal complex
|
J:81811
|
abnormal telomere morphology
|
J:81811
|
increased male germ cell apoptosis
|
J:81811
|
Ube2btm1Jhjh/Ube2btm1Jhjh
(involves: 129P2/OlaHsd * FVB/NJ)
|
abnormal sperm head morphology
|
J:35244
|
abnormal sperm midpiece morphology
|
J:35244
|
abnormal spermatocyte morphology
|
J:35244
|
asthenozoospermia
|
J:35244
|
increased male germ cell apoptosis
|
J:35244
|
oligozoospermia
|
J:35244
|
teratozoospermia
|
J:35244
|
Ube2btm1Jhjh/Ube2btm1Jhjh
(involves: 129P2/OlaHsd)
|
abnormal double-strand DNA break repair
|
J:177475
|
Ube2btm1Jhjh/Ube2btm1Jhjh
(involves: 129 * C57BL/6)
|
abnormal manchette morphology
|
J:83771
|
abnormal outer dense fiber morphology
|
J:83771
|
abnormal sperm fibrous sheath morphology
|
J:83771
|
abnormal sperm flagellum morphology
|
J:83771
|
abnormal spermatid morphology
|
J:83771
|
ectopic manchette
|
J:83771
|
Ube2cem1Gpt/Ube2cem1Gpt
(C57BL/6J-Ube2cem1Gpt)
|
decreased cell proliferation
|
J:333347
|
Ube2itm1.1Adej/Ube2itm1.1Adej
(involves: 129S1/Sv * BALB/c * C57BL/6)
|
abnormal inner cell mass apoptosis
|
J:104945
|
Ube2j1tm1.2Hpl/Ube2j1tm1.2Hpl
(involves: BALB/cJ * C57BL/6 * C57BL/6N * SJL)
|
abnormal acrosome morphology
|
J:218292
|
abnormal spermatid morphology
|
J:218292
|
absent sperm head
|
J:218292
|
asthenozoospermia
|
J:218292
|
teratozoospermia
|
J:218292
|
Ube2kGt(XK109)Byg/Ube2k+
(involves: 129P2/OlaHsd)
|
decreased neuron apoptosis
|
J:138978
|
Ube2kGt(XK109)Byg/Ube2kGt(XK109)Byg
(involves: 129P2/OlaHsd)
|
decreased neuron apoptosis
|
J:138978
|
Ube2nGt(OST374154)Lex/Ube2n+
(involves: 129S5/SvEvBrd * C57BL/6)
|
decreased B cell proliferation
|
J:120846
|
decreased T cell proliferation
|
J:120846
|
Ube2otm1.1(KOMP)Mbp/Ube2otm1.1(KOMP)Mbp
(involves: C57BL/6 * C57BL/6N * FVB/N)
|
abnormal cell migration
|
J:239679
|
abnormal cell physiology
|
J:239679
|
decreased fibroblast proliferation
|
J:239679
|
Ube2q1tm1Grz/Ube2q1tm1Grz
(involves: 129S1/Sv * 129X1/SvJ)
|
maternal effect
|
J:195898
|
Ube2stm1.1Smoc/Ube2stm1.1Smoc
(Not Specified)
|
abnormal female meiosis
|
J:346998
|
abnormal female meiosis I arrest
|
J:346998
|
Ube2wtm1d(EUCOMM)Wtsi/Ube2wtm1d(EUCOMM)Wtsi
(involves: 129 * C57BL/6N)
|
azoospermia
|
J:230053
|
cellular phenotype
|
J:230053
|
Ube3atm1Alb/Ube3a+
(involves: 129S7/SvEvBrd * C57BL/6)
|
paternal imprinting
|
J:130068,
J:50811
|
Ube3atm1Alb/Ube3atm1Alb
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased oocyte number
|
J:99980
|
oligozoospermia
|
J:99980
|
Ube3atm1Yelg/Ube3a+
(involves: 129P2/OlaHsd * 129S2/SvPasCrl)
|
paternal imprinting
|
J:222400
|
Ube3btm1a(EUCOMM)Hmgu/Ube3btm1a(EUCOMM)Hmgu
(C57BL/6-Ube3btm1a(EUCOMM)Hmgu)
|
abnormal mitochondrial physiology
|
J:273879
|
Ube4btm1Kei/Ube4btm1Kei
(involves: C57BL/6)
|
abnormal cell physiology
|
J:103761
|
increased cardiomyocyte apoptosis
|
J:103761
|
Ubiad1em1Wwk/Ubiad1+
(C57BL/6N-Ubiad1em1Wwk)
|
abnormal mitochondrial morphology
|
J:268574
|
Ubiad1em1Wwk/Ubiad1em1Wwk
(C57BL/6N-Ubiad1em1Wwk)
|
abnormal mitochondrial crista morphology
|
J:268574
|
abnormal mitochondrial morphology
|
J:268574
|
increased mitochondrial DNA content
|
J:268574
|
Ubr1tm1Avar/Ubr1tm1Avar Ubr2tm1Ytkw/Ubr2tm1Ytkw
(involves: 129S1/Sv * C57BL/6)
|
abnormal neuron differentiation
|
J:109036
|
increased neural tube apoptosis
|
J:109036
|
Ubr2tm1Ytkw/Ubr2tm1Ytkw
(involves: 129S1/Sv * C57BL/6)
|
arrest of male meiosis
|
J:86438
|
increased embryonic tissue cell apoptosis
|
J:86438
|
oligozoospermia
|
J:86438
|
Ubr4tm1.1Ytkw/Ubr4tm1.1Ytkw
(involves: 129P2/OlaHsd)
|
abnormal autophagy
|
J:196073
|
Ubr4tm1.2Nkt/Ubr4tm1.2Nkt Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL)
|
abnormal cell death
|
J:203460
|
increased cell proliferation
|
J:203460
|
Ubr5tm1Ckww/Ubr5tm1Ckww
(involves: 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:92269
|
increased embryonic tissue cell apoptosis
|
J:92269
|
Uchl1tm1Dgen/Uchl1tm1Dgen
(B6.129P2-Uchl1tm1Dgen/Mmnc)
|
abnormal mitochondrial physiology
|
J:361266
|
abnormal oocyte morphology
|
J:361266
|
decreased oocyte number
|
J:361266
|
maternal effect
|
J:361266
|
Uchl3tm1Tilg/Uchl3tm1Tilg
(involves: 129S1/Sv * C57BL/6J)
|
increased retina apoptosis
|
J:110169
|
Uchl5Gt(OST447189)Lex/Uchl5Gt(OST447189)Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal neuron differentiation
|
J:166694
|
Ucp1tm1Kz/Ucp1tm1Kz
(129S1.Cg-Ucptm1Kz)
|
abnormal mitochondrial physiology
|
J:69573
|
Ucp1tm1Kz/Ucp1tm1Kz
(B6.Cg-Ucptm1Kz)
|
abnormal mitochondrial physiology
|
J:69573
|
Ucp1tm1Kz/Ucp1tm1Kz
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal mitochondrial physiology
|
J:57998
|
Ucp1tm1Kz/Ucp1tm1Kz
((129S1.Cg-Ucptm1Kz x B6.Cg-Ucptm1Kz)F1)
|
abnormal mitochondrial physiology
|
J:69573
|
Ucp2tm1Lowl/Ucp2tm1Lowl
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cellular respiration
|
J:96713
|
decreased mitochondrial fission
|
J:96713
|
increased susceptibility to dopaminergic neuron neurotoxicity
|
J:96713
|
Ucp2tm1Rcq/Ucp2tm1Rcq
(involves: 129X1/SvJ * C57BL/6)
|
abnormal mitochondrial physiology
|
J:107995,
J:133277
|
cellular phenotype
|
J:120450
|
decreased cellular sensitivity to oxidative stress
|
J:107995
|
decreased neuron apoptosis
|
J:107995
|
Ucp3tm1Brnd/Ucp3tm1Brnd
(B6.Cg-Ucp3tm1Brnd)
|
abnormal mitochondrial physiology
|
J:73905
|
Ucp3tm1Lowl/Ucp3tm1Lowl
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cellular respiration
|
J:62313
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:102104
|
Ucp3tm1Rei/Ucp3tm1Rei
(involves: 129S6/SvEvTac * Black Swiss)
|
abnormal mitochondrial physiology
|
J:62312
|
Ufl1tm1c(EUCOMM)Wtsi/Ufl1tm1c(EUCOMM)Wtsi Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+
(involves: 129S4/SvJae * C3H * C57BL/6 * C57BL/6N)
|
abnormal autophagy
|
J:238253
|
Ufm1tm1.1Kmts/Ufm1tm1.1Kmts Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * C57BL/6N * SJL)
|
increased brain apoptosis
|
J:240522
|
increased neuron apoptosis
|
J:240522
|
Ugcgtm1Rlp/Ugcgtm1Rlp
(involves: 129S6/SvEvTac)
|
increased ectoderm apoptosis
|
J:80111,
J:76736
|
Ugcgtm1Rlp/Ugcgtm2Rlp
(involves: 129S6/SvEvTac)
|
abnormal plasma membrane morphology
|
J:76736
|
Uggt1Gt(RST539)Byg/Uggt1Gt(RST539)Byg
(involves: 129 * C57BL/6)
|
abnormal endoplasmic reticulum physiology
|
J:255869
|
Ugt1tm1.1Afmu/Ugt1tm1.1Afmu
(involves: 129 * C57BL/6 * SJL)
|
increased neuron apoptosis
|
J:182805
|
Uhmk1tm1Enbl/Uhmk1tm1Enbl
(involves: 129/Sv * C57BL/6)
|
abnormal cell cycle
|
J:144737
|
abnormal cell migration
|
J:144737
|
Uhrf1tm1Hko/Uhrf1tm1Hko
(Not Specified)
|
abnormal DNA methylation
|
J:129097
|
Uhrf1tm1Smoc/Uhrf1tm1Smoc Tg(Amh-cre)8815Reb/0
(involves: C57BL/6J * FVB/N)
|
abnormal cell cycle
|
J:324178
|
abnormal DNA methylation
|
J:324178
|
decreased male germ cell number
|
J:324178
|
decreased Sertoli cell proliferation
|
J:324178
|
increased male germ cell apoptosis
|
J:324178
|
Uhrf2em1Yoz/Uhrf2em1Yoz
(FVB/N-Uhrf2em1Yoz)
|
abnormal DNA methylation
|
J:241384
|
Uimc1Gt(RRN158)Byg/Uimc1Gt(RRN158)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal DNA repair
|
J:188388
|
chromosome breakage
|
J:188388
|
increased cellular sensitivity to gamma-irradiation
|
J:188388
|
Uimc1tm1.2Amj/Uimc1tm1.2Amj
(involves: BALB/cJ * C57BL/6)
|
abnormal cell cycle checkpoint function
|
J:191827
|
decreased fibroblast proliferation
|
J:191827
|
early cellular replicative senescence
|
J:191827
|
Ulk1tm1.1Thsn/Ulk1tm1.1Thsn
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
abnormal autophagy
|
J:139213
|
abnormal mitochondrial morphology
|
J:139213
|
Ulk4tm1a(KOMP)Wtsi/Ulk4tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal brain ependyma motile cilium morphology
|
J:234631
|
abnormal brain ependyma motile cilium physiology
|
J:234631
|
absent brain ependyma motile cilia
|
J:234631
|
Ulk4tm1Lex/Ulk4tm1Lex
(involves: 129S5/SvEvBrd * C57BL/6J)
|
abnormal respiratory motile cilium morphology
|
J:185566
|
decreased brain ependyma motile cilium length
|
J:185566
|
Umodem1Duf/Umod+
(C57BL/6J-Umodem1Duf)
|
abnormal autophagy
|
J:252597
|
increased endoplasmic reticulum stress
|
J:252597
|
increased kidney apoptosis
|
J:252597
|
UmodUrehd1/Umod+
(involves: C3HeB/FeJ)
|
abnormal endoplasmic reticulum morphology
|
J:201084
|
Unc5atm1Lhck/Unc5atm1Lhck
(involves: 129P2/OlaHsd)
|
decreased neuron apoptosis
|
J:111725
|
Unc5btm1Matl/Unc5btm1Matl
(involves: 129P2/OlaHsd * CD-1)
|
abnormal apoptosis
|
J:126240
|
Unc5crcm/Unc5crcm
(B6C3Fe a/a-Unc5crcm/J)
|
abnormal neuronal migration
|
J:45577
|
Unc5dtm1Kln/Unc5dtm1Kln
(involves: 129S/SvEv * C57BL/6)
|
abnormal axon extension
|
J:196042
|
abnormal neuronal migration
|
J:196042
|
Unc93b1tm1.1Kmiy/Unc93b1tm1.1Kmiy
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased B cell proliferation
|
J:174308
|
increased B cell proliferation
|
J:174308
|
Ungtm1Mend/Ungtm1Mend
(involves: 129S4/SvJae * BALB/c)
|
increased cellular sensitivity to oxidative stress
|
J:90910
|
Ungtm1Tld/Ungtm1Tld
(involves: 129P2/OlaHsd)
|
abnormal base-excision repair
|
J:197809
|
increased sensitivity to induced cell death
|
J:197809
|
Uoxem1Cli/Uoxem1Cli
(C57BL/6J-Uoxem1Cli)
|
increased pancreatic beta cell apoptosis
|
J:271949
|
Upf1tm1Hcd/Upf1tm1Hcd
(involves: 129X1/SvJ * C57BL/6)
|
increased apoptosis
|
J:67076
|
Upf2tm1Btp/Upf2tm1Btp En1tm2(cre)Wrst/En1+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
increased neuron apoptosis
|
J:306384
|
increased neuronal precursor proliferation
|
J:306384
|
Upf2tm1Btp/Upf2tm1Btp Tg(Atoh1-cre)1Bfri/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
increased neuronal precursor proliferation
|
J:306384
|
Upf2tm1Btp/Upf2tm1Btp Tg(Mx1-cre)1Cgn/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
decreased T cell proliferation
|
J:134765
|
Upf3atm1.1Wilk/Upf3atm1.1Wilk Tg(Stra8-icre)1Reb/0
(involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/NJ)
|
abnormal cell physiology
|
J:234504
|
abnormal male meiosis
|
J:234504
|
abnormal spermatocyte morphology
|
J:234504
|
abnormal spermatogonia morphology
|
J:234504
|
cellular phenotype
|
J:234504
|
decreased male germ cell number
|
J:234504
|
decreased spermatid number
|
J:234504
|
increased male germ cell apoptosis
|
J:234504
|
oligozoospermia
|
J:234504
|
Upf3bGt(IST14619B5)Tigm/Y
(involves: C57BL/6J * C57BL/6N)
|
impaired neuron differentiation
|
J:253157
|
increased neuronal precursor proliferation
|
J:253157
|
Upf3bGt(IST14619B5)Tigm/Upf3bGt(IST14619B5)Tigm
(involves: C57BL/6J * C57BL/6N)
|
impaired neuron differentiation
|
J:253157
|
increased neuronal precursor proliferation
|
J:253157
|
Upk1aem2Mgef/Upk1aem2Mgef
(C57BL/6NJNcbs-Upk1aem2Mgef)
|
increased neuron apoptosis
|
J:345207
|
increased pancreatic beta cell apoptosis
|
J:345207
|
oligozoospermia
|
J:345207
|
Uqcc3em1Hya/Uqcc3em1Hya Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: C57BL/6 * DBA/2)
|
abnormal mitochondrial morphology
|
J:306534
|
Uqcc6em1Lenh/Uqcc6em1Lenh
(C57BL/6J-Uqcc6em1Lenh)
|
abnormal respiratory electron transport chain
|
J:330815
|
Uqcrfs1tm1.1Hek/Uqcrfs1+
(involves: C57BL/6)
|
abnormal respiratory electron transport chain
|
J:179765
|
Uqcrfs1tm1Ctm/Uqcrfs1tm1Ctm Tg(Camk2a-cre)#Szi/0
(involves: 129 * C57BL/6 * C57BL/6J * CBA)
|
abnormal mitochondrial physiology
|
J:188773
|
increased mitochondrial fission
|
J:188773
|
Urahplt2/Urahplt2
(C57BL/6-Urahplt2)
|
increased T cell proliferation
|
J:267227
|
urehr1/urehr1
(C3HeB/FeJ-urehr1)
|
mesangial cell interposition
|
J:121470
|
Uri1tm1.1Ndj/Uri1tm1.1Ndj Albtm1(cre/ERT2)Mtz/Alb+
(B6.Cg-Albtm1(cre/ERT2)Mtz Uri1tm1.1Ndj)
|
increased hepatocyte apoptosis
|
J:217463
|
Use1tm1.1Aha/Use1tm1.2Aha
(involves: BALB/cJ * C57BL/6 * SJL)
|
abnormal endoplasmic reticulum morphology
|
J:147771
|
increased endoplasmic reticulum stress
|
J:147771
|
increased fibroblast apoptosis
|
J:147771
|
Ush1gtm1.2Ugds/Ush1gtm1.2Ugds
(involves: 129S1/SvImJ * BALB/c * C57BL/6 * C57BL/6J)
|
abnormal outer hair cell kinocilium location or orientation
|
J:171218
|
Uso1Gt(AW0562)Wtsi/Uso1Gt(AW0562)Wtsi
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal Golgi apparatus morphology
|
J:195576
|
Uso1Gt(YTA025)Byg/Uso1Gt(YTA025)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal Golgi apparatus morphology
|
J:195576
|
Usp1tm1.1Ada/Usp1tm1.1Ada
(C57BL/6-Usp1tm1.1Ada)
|
abnormal male germ cell morphology
|
J:146616
|
abnormal spermatocyte morphology
|
J:146616
|
absent spermatogonia
|
J:146616
|
decreased oocyte number
|
J:146616
|
decreased spermatid number
|
J:146616
|
induced chromosome breakage
|
J:146616
|
oligozoospermia
|
J:146616
|
Usp2tm1.1Ssw/Usp2tm1.1Ssw
(involves: C57BL/6)
|
abnormal male germ cell morphology
|
J:176705
|
abnormal sperm motility
|
J:176705
|
Usp4tm1Xilu/Usp4tm1Xilu
(B6.129-Usp4tm1Xilu)
|
abnormal cell physiology
|
J:173192
|
early cellular replicative senescence
|
J:173192
|
increased cellular sensitivity to ionizing radiation
|
J:173192
|
increased cellular sensitivity to ultraviolet irradiation
|
J:173192
|
increased splenocyte apoptosis
|
J:173192
|
increased thymocyte apoptosis
|
J:173192
|
Usp6nltm1.1Ppdf/Usp6nltm1.1Ppdf
(involves: C57BL/6)
|
increased fibroblast cell migration
|
J:247704
|
increased fibroblast chemotaxis
|
J:247704
|
Usp8tm1.1Kpk/Usp8tm1.1Kpk Tg(Mx1-cre)1Cgn/0
(involves: 129P2/OlaHsd * C57BL/6 * CBA * FVB/N)
|
increased hepatocyte apoptosis
|
J:122732
|
Usp9xtm1Tuv/Y Tg(Ddx4-cre)1Dcas/0
(involves: FVB)
|
abnormal spermatid morphology
|
J:243959
|
abnormal spermatocyte morphology
|
J:243959
|
increased male germ cell apoptosis
|
J:243959
|
oligozoospermia
|
J:243959
|
Usp10tm1Fuj/Usp10tm1Fuj
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal cell morphology
|
J:194412
|
increased apoptosis
|
J:194412
|
oxidative stress
|
J:194412
|
Usp11tm1Tac/Y
(involves: 129 * C57BL/6)
|
abnormal fibroblast physiology
|
J:270214
|
increased fibroblast proliferation
|
J:270214
|
Usp14ax-J/Usp14ax-J
(B6.Cg-Usp14ax-J/J)
|
increased neuron apoptosis
|
J:108034
|
Usp17lctm1Khb/Usp17lc+
(either: 129-Usp17lctm1Khb or (involves: 129S/SvEv * C57BL/6J))
|
asthenozoospermia
|
J:191761
|
Usp17lctm1Khb/Usp17lctm1Khb
(either: 129-Usp17lctm1Khb or (involves: 129S/SvEv * C57BL/6J))
|
decreased cell proliferation
|
J:191761
|
increased embryonic tissue cell apoptosis
|
J:191761
|
increased trophectoderm apoptosis
|
J:191761
|
Usp19Gt(XG128)Byg/Usp19Gt(XG128)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal autophagy
|
J:225526
|
Usp22tm1a(KOMP)Wtsi/Usp22tm1a(KOMP)Wtsi
(C57BL/6-Usp22tm1a(KOMP)Wtsi)
|
abnormal cell differentiation
|
J:233975
|
abnormal intestinal villus goblet cell morphology
|
J:233975
|
impaired neuron differentiation
|
J:233975
|
Usp22tm1Dfan/Usp22tm1Dfan
(C57BL/6-Usp22tm1Dfan)
|
increased fibroblast apoptosis
|
J:188021
|
Usp24Gt(XB614)Byg/Usp24Gt(XB614)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
chromosomal instability
|
J:303991
|
Usp26tm1Smoc/Y
(B6.129S6-Usp26tm1Smoc)
|
decreased male germ cell number
|
J:277424
|
oligozoospermia
|
J:277424
|
Usp28Gt(EUCE0037g10)Hmgu/Usp28Gt(EUCE0037g10)Hmgu
(involves: 129P2/OlaHsd * C57BL/6J)
|
cellular phenotype
|
J:215354
|
induced chromosome breakage
|
J:215354
|
Usp29tm1Jkim/Usp29+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
paternal effect
|
J:249082
|
Usp29tm1Jkim/Usp29+
(involves: 129S7/SvEvBrd * C57BL/6J * PWD/PhJ)
|
abnormal DNA methylation
|
J:249082
|
Usp30tm1.1Tac/Usp30tm1.1Tac
(B6(Cg)-Usp30tm1.1Tac)
|
abnormal cellular respiration
|
J:286265
|
abnormal mitophagy
|
J:286265
|
Usp36Gt(EUCE00141e03)Hmgu/Usp36Gt(EUCE00141e03)Hmgu
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:257189
|
increased embryonic tissue cell apoptosis
|
J:257189
|
Usp42tm2a(EUCOMM)Wtsi/Usp42tm2a(EUCOMM)Wtsi
(involves: C57BL/6 * C57BL/6N)
|
oligozoospermia
|
J:213427
|
Usp44tm1.2Pjgl/Usp44tm1.2Pjgl
(involves: 129S4/SvJae * 129S7/SvEvBrd)
|
abnormal mitotic spindle morphology
|
J:193965
|
aneuploidy
|
J:193965
|
chromosomal instability
|
J:193965
|
Usp47Gt(RRJ301)Byg/Usp47Gt(RRJ301)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:166002
|
Utf1tm1Okud/Utf1tm1Okud
(B6.129P2-Utf1tm1Okud)
|
decreased cell proliferation
|
J:204409
|
Utp14bjsd/Utp14bjsd
(involves: C3H/HeJ * C57BL/6J)
|
azoospermia
|
J:91782
|
UvragTn(pb-Act-RFP)1.100107015-HRAZhu/UvragTn(pb-Act-RFP)1.100107015-HRAZhu
(involves: FVB/NJ)
|
abnormal autophagy
|
J:219546
|
abnormal lysosome morphology
|
J:219546
|
cardiac interstitial fibrosis
|
J:219546
|
increased cardiomyocyte apoptosis
|
J:219546
|
Vac14Gt(RRP155)Byg/Vac14Gt(RRP155)Byg
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal vacuole morphology
|
J:127106
|
increased forebrain apoptosis
|
J:127106
|
increased hindbrain apoptosis
|
J:127106
|
increased midbrain apoptosis
|
J:127106
|
Vamp7tm1.1Aha/Y
(involves: 129S4/SvJae)
|
abnormal axon extension
|
J:197602
|
Vamp7tm1.1Aha/Vamp7tm1.1Aha
(involves: 129S4/SvJae)
|
abnormal axon extension
|
J:197602
|
Vamp8tm1Hong/Vamp8tm1Hong
(involves: 129P2/OlaHsd * C57BL/6)
|
decreased mast cell degranulation
|
J:133439
|
Vangl1Gt(XL802)Byg/Vangl1Gt(XL802)Byg Vangl2tm1.2Yy/Vangl2tm1.2Yy
(involves: 129P2/OlaHsd * C57BL/6 * CBA)
|
abnormal embryonic cilium location or orientation
|
J:162640
|
abnormal motile primary cilium physiology
|
J:162640
|
Vapbtm1.2Ics/Vapbtm1.2Ics
(B6N.129S2-Vapbtm1.2Ics)
|
cellular phenotype
|
J:198145
|
Vasntm1Zgl/Vasntm1Zgl
(B6.Cg-Vasntm1Zgl)
|
abnormal male germ cell apoptosis
|
J:173568
|
increased apoptosis
|
J:173568
|
increased cellular sensitivity to hydrogen peroxide
|
J:173568
|
increased cellular sensitivity to ultraviolet irradiation
|
J:173568
|
increased hepatocyte apoptosis
|
J:173568
|
increased sensitivity to induced cell death
|
J:173568
|
oxidative stress
|
J:173568
|
Vav1tm1Tyb/Vav1tm1Tyb
(involves: 129S2/SvPas * 129S8/SvEv)
|
decreased T cell proliferation
|
J:113270
|
Vav1tm1Tyb/Vav1tm1Tyb
(involves: 129S2/SvPas)
|
decreased T cell proliferation
|
J:86654
|
Vav1tm1Tyb/Vav1tm1Tyb
(involves: 129S2/SvPas * C57BL/10 * C57BR/cd)
|
decreased T cell proliferation
|
J:128985
|
Vav1tm1Tyb/Vav1tm1Tyb Vav2tm1Kdf/Vav2tm1Kdf
(involves: 129S1/Sv * 129S2/SvPas)
|
decreased B cell proliferation
|
J:86654
|
decreased T cell proliferation
|
J:86654
|
Vav1tm1Tyb/Vav1tm1Tyb Vav2tm1Kdf/Vav2tm1Kdf Vav3tm1Swat/Vav3tm1Swat
(involves: 129S1/Sv * 129S2/SvPas * 129S6/SvEvTac * C57BL/6)
|
decreased B cell proliferation
|
J:86654
|
decreased T cell proliferation
|
J:86654
|
Vav1tm1Tyb/Vav1tm1Tyb Vav2tm1Tnr/Vav2tm1Tnr
(involves: 129P2/OlaHsd * 129S2/SvPas)
|
decreased B cell proliferation
|
J:69807
|
Vav1tm1Tyb/Vav1tm1Tyb Vav3tm1Swat/Vav3tm1Swat
(involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6)
|
decreased B cell proliferation
|
J:86654
|
decreased T cell proliferation
|
J:86654
|
Vav1tm2Bbd/Vav1tm2Bbd
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
decreased T cell proliferation
|
J:47596
|
Vav1tm2Bbd/Vav1tm2Bbd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased B cell proliferation
|
J:55647,
J:69806
|
Vav1tm2Bbd/Vav1tm2Bbd Vav2tm1Kdf/Vav2tm1Kdf
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6)
|
decreased B cell proliferation
|
J:69806
|
Vav1tm2Tyb/Vav1tm2Tyb
(involves: 129S4/SvJae * 129S8/SvEv)
|
decreased T cell proliferation
|
J:113270
|
Vav2tm1Kdf/Vav2tm1Kdf
(involves: 129S1/Sv * C57BL/6)
|
decreased B cell proliferation
|
J:69806
|
Vav2tm1Tnr/Vav2tm1Tnr
(involves: 129P2/OlaHsd)
|
decreased B cell proliferation
|
J:69807
|
Vav2tm1Tnr/Vav2tm1Tnr Vav3tm1Swat/Vav3tm1Swat
(involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6)
|
abnormal axon guidance
|
J:98310
|
Vav2tm1Tnr/Vav2tm1Tnr Vav3tm1Swat/Vav3tm1Swat
(involves: 129P2/OlaHsd * 129S6/SvEvTac)
|
abnormal cell adhesion
|
J:110334
|
abnormal vascular endothelial cell migration
|
J:110334
|
Vax1tm1Grl/Vax1tm1Grl
(involves: 129S1/Sv * C57BL/6)
|
abnormal axon guidance
|
J:58996
|
abnormal neuron differentiation
|
J:96805
|
Vax2tm1Grl/Vax2tm1Grl
(involves: 129S1/Sv * C57BL/6)
|
abnormal axon guidance
|
J:74240
|
Vcam1tm1Dmil/Vcam1tm1Dmil
(C.129S4-Vcam1tm1Dmil)
|
decreased cell chemotaxis
|
J:227109
|
Vcam1tm1Dmil/Vcam1tm1Dmil
(involves: 129S4/SvJae)
|
decreased cell chemotaxis
|
J:227109
|
Vcam1tm2Dmil/Vcam1tm2Dmil
(B6.129S4-Vcam1tm2Dmil)
|
decreased cell chemotaxis
|
J:227109
|
Vcam1tm2Flv/Vcam1tm3Flv Tg(Tek-cre)12Flv/0
(involves: 129S1/Sv * C3H * C57BL/6)
|
impaired B cell migration
|
J:68147
|
Vcltm1.1Whz/Vcltm1.1Whz
(involves: 129/Sv * C57BL/6 * SJL)
|
abnormal cell adhesion
|
J:163108
|
increased apoptosis
|
J:163108
|
increased embryonic neuroepithelium apoptosis
|
J:163108
|
Vcltm1Eda/Vcltm1Eda
(involves: 129S1/Sv * 129X1/SvJ * Black Swiss)
|
abnormal cell adhesion
|
J:45781
|
increased fibroblast proliferation
|
J:45781
|
Vcpem1Kene/Vcp+
(C57BL/6J-Vcpem1Kene)
|
cellular phenotype
|
J:325062
|
Vcptm1.1Hiok/Vcp+
(B6(Cg)-Vcptm1.1Hiok)
|
abnormal cell cycle checkpoint function
|
J:308471
|
abnormal DNA repair
|
J:308471
|
abnormal endoplasmic reticulum morphology
|
J:308471
|
cellular necrosis
|
J:308471
|
cellular phenotype
|
J:308471
|
Vcptm1Itl/Vcp+
(B6.129S-Vcptm1Itl)
|
abnormal autophagy
|
J:166230
|
abnormal osteoclast differentiation
|
J:166230
|
Vcptm1Itl/Vcptm1Itl
(involves: 129S6/SvEvTac)
|
abnormal autophagy
|
J:191963
|
abnormal mitochondrial crista morphology
|
J:191963
|
increased mitochondrial fission
|
J:191963
|
Vcpip1em1Zlou/Vcpip1em1Zlou
(C57BL/6NHsd-Vcpip1em1Zlou)
|
abnormal chromosome morphology
|
J:297179
|
abnormal DNA repair
|
J:297179
|
chromosomal instability
|
J:297179
|
increased cellular sensitivity to DNA damaging agents
|
J:297179
|
Vdac2tm1.1Ehyc/Vdac2tm1.1Ehyc Tg(Lck-cre)1Cwi/?
(involves: 129X1/SvJ * C57BL/6 * DBA/2)
|
abnormal thymocyte apoptosis
|
J:220951
|
Vdac3em1Kei/Vdac3em1Kei
(C57BL/6J-Vdac3em1Kei)
|
abnormal sperm mitochondrial sheath morphology
|
J:332977
|
asthenozoospermia
|
J:332977
|
decreased sperm mitochondrial sheath size
|
J:332977
|
kinked sperm flagellum
|
J:332977
|
Vdac3tm1Wjc/Vdac3tm1Wjc
(Not Specified)
|
abnormal respiratory electron transport chain
|
J:72188
|
abnormal skeletal muscle fiber mitochondrial shape
|
J:72188
|
abnormal sperm axoneme morphology
|
J:72188
|
abnormal sperm mitochondrial morphology
|
J:72188
|
asthenozoospermia
|
J:72188
|
decreased sperm progressive motility
|
J:72188
|
Vdrtm1Ska/Vdrtm1Ska
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal macrophage chemotaxis
|
J:112519
|
asthenozoospermia
|
J:83237
|
decreased splenocyte proliferation
|
J:112519
|
oligozoospermia
|
J:83237
|
Vdrtm1Ska/Vdrtm1Ska
(NOD.Cg-Vdrtm1Ska/CmatJ)
|
abnormal dendritic cell differentiation
|
J:127787
|
Vegfatm1Dco/Vegfatm1Dco
(involves: 129)
|
abnormal vascular endothelial cell differentiation
|
J:32219
|
Vegfatm1Gne/Vegfa+
(involves: 129S2/SvPas * C57BL/6J)
|
increased embryonic neuroepithelium apoptosis
|
J:32218
|
increased embryonic tissue cell apoptosis
|
J:32218
|
Vegfatm1Pec/Vegfatm1Pec
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal mesangial cell morphology
|
J:111504
|
abnormal neuronal migration
|
J:94050
|
abnormal vascular regression
|
J:81698
|
increased neuron apoptosis
|
J:175836
|
Vegfatm2Gne/Vegfatm2.1Nagy Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * SJL)
|
abnormal neuron proliferation
|
J:86207
|
Vegfatm2Gne/Vegfatm2Gne Tg(Nphs1-cre)1Seq/0
(involves: 129)
|
abnormal mesangial cell morphology
|
J:82440
|
Vegfatm2Gne/Vegfatm2Gne Tg(SFTPC-rtTA)5Jaw/0 Tg(tetO-cre)1Jaw/0
(involves: 129 * C57BL/6)
|
decreased mesenchymal cell proliferation involved in lung development
|
J:124125
|
Vegfatm4Pec/Vegfatm4Pec
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal vascular regression
|
J:81698
|
Vezttm1.1Smc/Vezttm1.1Smc
(either: (involves: 129S2/SvPas * BALB/c * C57BL/6 * MF1) or (involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6N * MF1))
|
abnormal cell adhesion
|
J:121686
|
Vgll4tm1b(EUCOMM)Hmgu/Vgll4tm1b(EUCOMM)Hmgu
(involves: C57BL/6N * CBA)
|
increased cell proliferation
|
J:273437
|
Vgll4tm1b(EUCOMM)Hmgu/Vgll4tm1c(EUCOMM)Hmgu Tg(Tek-cre)1Ywa/0
(involves: C57BL/6N * CBA * SJL)
|
decreased apoptosis
|
J:273437
|
increased cell proliferation
|
J:273437
|
Vhltm1.1Whkr/Vhltm1.1Whkr
(involves: 129S4/SvJae * C57BL/6)
|
abnormal intracellular organelle physiology
|
J:198361
|
Vhltm1Jae/Vhltm1Jae
(involves: 129S4/SvJae)
|
decreased cell proliferation
|
J:160941
|
Vhltm1Jae/Vhltm1Jae Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129S4/SvJae * C57BL/6 * DBA)
|
increased hepatocyte proliferation
|
J:144666
|
Vhltm1Jae/Vhltm1Jae Tg(KRT14-cre)1Ipc/0
(involves: 129S4/SvJae * C57BL/6 * SJL)
|
increased keratinocyte proliferation
|
J:144666
|
Vhltm1Jae/Vhltm1Jae Tg(Myh6-cre)2182Mds/0
(involves: 129S4/SvJae * FVB/N)
|
decreased mitochondrial number
|
J:179490
|
Vhltm1Jae/Vhltm1Jae Tg(NPHS2-cre)295Lbh/?
(involves: 129S4/SvJae * C57BL/6 * SJL)
|
increased mesangial cell number
|
J:162099
|
Vhltm1Lss/Vhltm1.1Lss
(involves: 129X1/SvJ * C57BL/6)
|
oligozoospermia
|
J:85513
|
Vhltm1Lss/Vhltm1.1Lss Tg(ACTB-cre)1Tes/0
(involves: 129X1/SvJ * C3H * C57BL/6)
|
multinucleated giant male germ cells
|
J:85513
|
oligozoospermia
|
J:85513
|
Vhltm1Lss/Vhltm1.1Lss Tg(CAG-cre/Esr1*)1Lbe/0
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased renal tubule apoptosis
|
J:155367
|
Vimtm1Cba/Vimtm1Cba
(involves: 129S2/SvPas)
|
abnormal cell migration
|
J:118721
|
abnormal cell morphology
|
J:118721
|
abnormal cell physiology
|
J:118721
|
Vimtm1Cba/Vimtm1Cba
(involves: 129S2/SvPas * C57BL/6)
|
abnormal cellular extravasation
|
J:129405
|
abnormal leukocyte adhesion
|
J:129405
|
abnormal leukocyte migration
|
J:129405
|
abnormal leukocyte tethering or rolling
|
J:129405
|
cellular phenotype
|
J:125280,
J:125659
|
Vimtm2Cba/Vimtm2Cba
(involves: 129S2/SvPas)
|
abnormal cell migration
|
J:118721
|
abnormal cell morphology
|
J:118721
|
abnormal cell physiology
|
J:118721
|
Vipr1tm1Msod/Vipr1tm1Msod
(B6.129-Vipr1tm1Msod)
|
abnormal enterocyte proliferation
|
J:177616
|
Vittm1Koth/Vittm1Koth
(B6J.Cg-Vittm1Koth)
|
abnormal neuron differentiation
|
J:237454
|
Vps4atm1.2Thkn/Vps4a+ Vps4btm1Thkn/Vps4b+
(B6.129S2(Cg)-Vps4btm1Thkn Vps4atm1.2Thkn)
|
abnormal cell morphology
|
J:236761
|
Vps13atm1Asan/Vps13atm1Asan
(129S6.129S(B6)-Vps13atm1Asan)
|
abnormal sperm mitochondrial morphology
|
J:270605
|
asthenozoospermia
|
J:270605
|
Vps13btm1.2Ics/Vps13btm1.2Ics
(involves: C57BL/6N)
|
abnormal acroplaxome morphology
|
J:296169
|
abnormal actin cytoskeleton morphology
|
J:296169
|
abnormal Golgi apparatus morphology
|
J:296169
|
abnormal Golgi stack morphology
|
J:296169
|
abnormal Golgi vesicle transport
|
J:296169
|
abnormal sperm nucleus morphology
|
J:296169
|
absent acrosome
|
J:296169
|
cellular phenotype
|
J:296169
|
globozoospermia
|
J:296169
|
increased male germ cell apoptosis
|
J:296169
|
multinucleated giant male germ cells
|
J:296169
|
necrospermia
|
J:296169
|
oligozoospermia
|
J:296169
|
teratozoospermia
|
J:296169
|
Vps18tm1.1Wtao/Vps18tm1.1Wtao Tg(Nes-cre)1Kln/0
(involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal autophagy
|
J:186307
|
abnormal neuronal migration
|
J:186307
|
increased neuron apoptosis
|
J:186307
|
Vps25m1Lis/Vps25m1Lis
(involves: C3H * C57BL/6J)
|
abnormal cell morphology
|
J:223082
|
increased apoptosis
|
J:223082
|
increased cell proliferation
|
J:223082
|
Vps35Gt(RRK261)Byg/Vps35+
(B6.129P2-Vps35Gt(RRK261)Byg)
|
abnormal lysosome morphology
|
J:225806
|
Vps35tm1.1Hckn/Vps35tm1.1Hckn Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129P2/OlaHsd * C57BL/6 * DBA/2)
|
abnormal small intestinal crypt cell proliferation
|
J:223191
|
Vps35tm1.1Hlw/Vps35+
(involves: 129S/SvEv * C57BL/6J)
|
abnormal mitochondrial shape
|
J:329507
|
decreased mitochondrial size
|
J:329507
|
oxidative stress
|
J:329507
|
Vps35tm1.1Mjff/Vps35tm1.1Mjff
(B6.Cg-Vps35tm1.1Mjff)
|
abnormal mitochondrial physiology
|
J:303283
|
abnormal mitochondrial shape
|
J:303283
|
Vps41tm1.1Ywd/Vps41tm1.1Ywd
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal endocytosis
|
J:184591
|
increased ectoderm apoptosis
|
J:184591
|
Vps54wr/Vps54wr
(multiple strains)
|
abnormal cell morphology
|
J:5525
|
abnormal endoplasmic reticulum morphology
|
J:5525
|
abnormal lysosome morphology
|
J:5525
|
asthenozoospermia
|
J:1563
|
globozoospermia
|
J:1563
|
oligozoospermia
|
J:1563
|
Vrk1Gt(RRR178)Byg/Vrk1Gt(RRR178)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal female meiosis
|
J:171525
|
abnormal oogenesis
|
J:171525
|
abnormal spermatogonia proliferation
|
J:156653
|
azoospermia
|
J:156653
|
decreased male germ cell number
|
J:156653,
J:171525
|
decreased spermatid number
|
J:156653
|
impaired polar body extrusion
|
J:171525
|
Vrk1Gt(RRR178)Byg/Vrk1Gt(RRR178)Byg
(B6.129P2-Vrk1Gt(RRR178)Byg)
|
abnormal oocyte morphology
|
J:207272
|
Vsig4tm1Gne/Vsig4tm1Gne
(C57BL/6-Vsig4tm1Gne)
|
abnormal enterocyte proliferation
|
J:281762
|
Vsx2or-J/Vsx2or-J
(129S1/Sv)
|
abnormal cell death
|
J:5966
|
Vsx2or/Vsx2or
(involves: C57BL/Gr)
|
abnormal cell cycle checkpoint function
|
J:5575
|
vtab/vtab
(CBy.Cg-vtab/GrsrJ)
|
decreased male germ cell number
|
J:237551
|
Vti1atm1Gfvm/Vti1atm1Gfvm Vti1btm1Gfvm/Vti1btm1Gfvm
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal axon extension
|
J:169107
|
abnormal axon guidance
|
J:169107
|
cellular phenotype
|
J:169107
|
increased neuron apoptosis
|
J:169107
|
Vti1btm1Gfvm/Vti1btm1Gfvm
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal lysosome physiology
|
J:84574
|
Wapltm1.1Jmpt/Wapltm1.2Jmpt Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+
(involves: 129 * C57BL/6 * C57BL/6NTac * SJL)
|
abnormal cell cycle
|
J:205429
|
abnormal mitosis
|
J:205429
|
absent fibroblast proliferation
|
J:205429
|
Wastm1Itl/Y
(Not Specified)
|
decreased T cell proliferation
|
J:153247
|
Wastm1Itl/Wastm1Itl
(Not Specified)
|
decreased T cell proliferation
|
J:153247
|
Wastm1Sbs/Y
(involves: 129S6/SvEvTac)
|
decreased T cell proliferation
|
J:153247
|
Wastm1Sbs/Wastm1Sbs
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6))
|
decreased T cell proliferation
|
J:48836
|
Wastm1Sbs/Wastm1Sbs
(involves: 129S/SvEv)
|
abnormal cell migration
|
J:84888
|
abnormal osteoclast differentiation
|
J:90542
|
Wastm1Sbs/Wastm1Sbs
(involves: BALB/c)
|
decreased T cell proliferation
|
J:84131
|
Wastm1Sbs/Wastm1Sbs
(involves: 129S6/SvEvTac)
|
decreased T cell proliferation
|
J:153247
|
Wastm1Sbs/Wastm1Sbs
(129S6/SvEvTac-Wastm1Sbs/J)
|
increased mesangial cell number
|
J:180407
|
Wastm2Itl/Y
(Not Specified)
|
decreased T cell proliferation
|
J:153247
|
Wastm2Itl/Wastm2Itl
(Not Specified)
|
decreased T cell proliferation
|
J:153247
|
Washc1tm1.1Xya/Washc1tm1.1Xya
(involves: 129 * FVB/N)
|
abnormal autophagy
|
J:202483
|
increased cell death
|
J:202483
|
Washc1tm1Xya/Washc1tm1Xya
(involves: 129)
|
abnormal autophagy
|
J:202483
|
Washc4em1Ssod/Washc4em1Ssod
(involves: C57BL/6J * SJL/J)
|
abnormal lysosome morphology
|
J:303795
|
increased neuron apoptosis
|
J:303795
|
lysosomal protein accumulation
|
J:303795
|
Washc5tm1.2Cbee/Washc5+
(involves: C57BL/6)
|
cellular phenotype
|
J:266630
|
Wasltm1.1Ttha/Wasltm1.1Ttha Tg(KRT14-cre)1Amc/0
(involves: C57BL/6 * C57BL/6N * CBA)
|
increased keratinocyte proliferation
|
J:271857
|
Wasltm1.1Ttha/Wasltm1.1Ttha Tg(Nes-cre)1Kag/0
(involves: C57BL/6 * SJL)
|
absent brain ependyma motile cilia
|
J:207484
|
Wasltm1Sbs/Wasltm1Sbs
(either: (involves: 129P2/OlaHsd * 129S/SvEv) or (involves: 129P2/OlaHsd * C57BL/6))
|
abnormal cell chemotaxis
|
J:72053
|
decreased fibroblast proliferation
|
J:72053
|
Wdfy3disc/Wdfy3disc
(involves: C57BL/6J * FVB/NJ)
|
abnormal cell cycle
|
J:225200
|
abnormal neuronal migration
|
J:225200
|
abnormal neuronal precursor proliferation
|
J:225200
|
cellular phenotype
|
J:225200
|
increased radial glial cell number
|
J:225200
|
premature neuronal precursor differentiation
|
J:225200
|
Wdfy3tm1a(KOMP)Mbp/Wdfy3tm1a(KOMP)Mbp
(C57BL/6N-Wdfy3tm1a(KOMP)Mbp)
|
abnormal neuronal migration
|
J:225200
|
Wdfy3Tn(pb-Act-RFP)1.1Zhu/Wdfy3Tn(pb-Act-RFP)1.1Zhu
(involves: C57BL/6 * FVB/NJ)
|
cellular phenotype
|
J:285853
|
Wdhd1em1Isyu/Wdhd1em1Isyu
(Not Specified)
|
decreased cell proliferation
|
J:306382
|
increased apoptosis
|
J:306382
|
Wdpcpcys40/Wdpcpcys40
(involves: C57BL/6J)
|
abnormal cell physiology
|
J:205269
|
abnormal cilium morphology
|
J:205269
|
abnormal kinocilium morphology
|
J:205269
|
abnormal podocyte motility
|
J:205269
|
impaired fibroblast cell migration
|
J:205269
|
Wdr1rede/Wdr1rede
(C57BL/6-Wdr1rede)
|
impaired neutrophil chemotaxis
|
J:134092
|
Wdr4em1Bcgen/Wdr4em1Bcgen
(involves: C57BL/6J)
|
decreased chondrocyte proliferation
|
J:355649
|
Wdr4tm1.1Hsi/Wdr4tm1.1Hsi
(involves: C57BL/6J * FVB/N)
|
increased embryonic tissue cell apoptosis
|
J:230030
|
Wdr11Gt(Ayu21-KBW205)Imeg/Wdr11Gt(Ayu21-KBW205)Imeg
(B6.Cg-Wdr11Gt(Ayu21-KBW205)Imeg)
|
abnormal neuronal migration
|
J:257035
|
abnormal olfactory epithelium cilium morphology
|
J:257035
|
abnormal primary cilium morphology
|
J:257035
|
teratozoospermia
|
J:257035
|
Wdr13tm1Kuma/Y
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
increased pancreatic beta cell proliferation
|
J:225111
|
Wdr19dmhd/Wdr19dmhd
(involves: FVB/NJ)
|
abnormal cilium morphology
|
J:181888
|
Wdr19twto/Wdr19twto
(involves: FVB/NJ)
|
abnormal cilium morphology
|
J:181888
|
Wdr35yeti/Wdr35yeti
(Not Specified)
|
absent embryonic cilia
|
J:171617
|
Wdr45em1Wrst/Y
(involves: C57BL/6N * FVB)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:307284
|
Wdr45em1Wrst/Wdr45em1Wrst
(involves: C57BL/6N * FVB)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:307284
|
Wdr45tm1Beij/Y Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL)
|
impaired autophagy
|
J:281235
|
Wdr45tm1Beij/Wdr45+ Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL)
|
impaired autophagy
|
J:281235
|
Wdr45tm1Beij/Wdr45tm1Beij Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6N * SJL)
|
impaired autophagy
|
J:281235
|
Wdr48Gt(CSD197)Byg/Wdr48+
(B6.129P2-Wdr48Gt(CSD197)Byg)
|
decreased male germ cell number
|
J:206106
|
decreased oocyte number
|
J:206106
|
Wdr62Gt(AF0003)Wtsi/Wdr62Gt(AF0003)Wtsi
(involves: 129P2/OlaHsd * 129S1/SvImJ)
|
abnormal mitosis
|
J:224504
|
abnormal mitotic spindle assembly checkpoint
|
J:224504
|
abnormal mitotic spindle morphology
|
J:224504
|
increased cell death
|
J:224504
|
Wdr62tm1.1Jfch/Wdr62tm1.1Jfch
(involves: 129S1/SvImJ * C57BL/6N)
|
abnormal cell cycle
|
J:282438
|
abnormal primary cilium morphology
|
J:282438
|
decreased cell proliferation
|
J:282438
|
increased forebrain apoptosis
|
J:282438
|
premature neuronal precursor differentiation
|
J:282438
|
Wdr62tm3a(EUCOMM)Hmgu/Wdr62tm3a(EUCOMM)Hmgu
(C57BL/6-Wdr62tm3a(EUCOMM)Hmgu)
|
abnormal male meiosis
|
J:306320
|
abnormal manchette disassembly
|
J:306320
|
abnormal sperm head morphology
|
J:306320
|
absent oocytes
|
J:306320
|
asthenozoospermia
|
J:306320
|
decreased sperm progressive motility
|
J:306320
|
oligozoospermia
|
J:306320
|
teratozoospermia
|
J:306320
|
Wdr81nur5/Wdr81nur5
(involves: C57BL/6J)
|
abnormal neuron mitochondrial morphology
|
J:196651
|
disorganized mitochondrial cristae
|
J:196651
|
increased mitochondrial size
|
J:196651
|
Wdr83tm1Guwo/Wdr83+
(involves: C57BL/6)
|
decreased renal tubule apoptosis
|
J:153983
|
Wdr91tm2Bcgen/Wdr91tm2Bcgen Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:247712
|
increased neuron apoptosis
|
J:247712
|
Wee1tm1.1Cxd/Wee1tm1.1Cxd
(involves: 129S6/SvEvTac * FVB/N)
|
abnormal cell cycle checkpoint function
|
J:228492
|
decreased embryonic epiblast cell proliferation
|
J:228492
|
increased cellular sensitivity to gamma-irradiation
|
J:228492
|
increased embryonic epiblast cell apoptosis
|
J:228492
|
Wfdc1tm1Bcm/Wfdc1tm1Bcm
(involves: 129S7/SvEvBrd * C57BL/6)
|
abnormal cell adhesion
|
J:216357
|
Wfdc2tm1.1Ohbo/Wfdc2tm1.1Ohbo
(involves: C57BL/6NCrlj * CBA/JNCrlj)
|
abnormal respiratory motile cilium morphology
|
J:282576
|
decreased respiratory motile cilia number
|
J:282576
|
Wfdc15aem1Ohbo/Wfdc15aem1Ohbo
(involves: Slc:ICR)
|
abnormal elongated spermatid morphology
|
J:360881
|
azoospermia
|
J:360881
|
decreased elongated spermatid number
|
J:360881
|
increased male germ cell apoptosis
|
J:360881
|
Wfs1tm1Koks/Wfs1tm1Koks
(129S6/SvEvTac-Wfs1tm1Koks)
|
abnormal sperm flagellum morphology
|
J:157127
|
abnormal sperm head morphology
|
J:157127
|
decreased male germ cell number
|
J:157127
|
decreased spermatogonia number
|
J:157127
|
increased sperm motility
|
J:157127
|
Wg5CAST/EiJ/Wg5CAST/EiJ
(involves: C57BL/6J * CAST/EiJ)
|
cellular phenotype
|
J:135426
|
Whammtm1b(KOMP)Wtsi/Whammtm1b(KOMP)Wtsi
(B6N(Cg)-Whammtm1b(KOMP)Wtsi/3J)
|
abnormal actin cytoskeleton morphology
|
J:349712
|
abnormal autophagosome formation
|
J:349712
|
abnormal autophagy
|
J:349712
|
Wipf1tm1Geha/Wipf1tm1Geha
(involves: 129S6/SvEvTac)
|
decreased T cell proliferation
|
J:74719
|
increased B cell proliferation
|
J:74719
|
Wipf3tm1Tta/Wipf3tm1Tta
(involves: 129P2/OlaHsd * C57BL/6J)
|
abnormal sperm head morphology
|
J:132529
|
abnormal spermatid morphology
|
J:132529
|
small sperm head
|
J:132529
|
teratozoospermia
|
J:132529
|
Wlsem1Jgg/Wlsem1Jgg
(involves: C57BL/6J)
|
abnormal neuron differentiation
|
J:341542
|
Wlsem2Jgg/Wlsem2Jgg
(involves: C57BL/6J)
|
abnormal neuron differentiation
|
J:341542
|
Wlstm1.1Arte/Wlstm1.1Arte Krt14tm1(cre)Wbm/Krt14+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased keratinocyte proliferation
|
J:202499
|
increased T cell proliferation
|
J:202499
|
Wlstm1Xzg/Wlstm1Xzg Tg(Msx2-cre)5Rem/0
(Not Specified)
|
decreased cell proliferation
|
J:184918
|
increased apoptosis
|
J:184918
|
Wlstm1Xzg/Wlstm1Xzg Tg(Prrx1-cre)1Cjt/0
(involves: C57BL/6J * SJL/J)
|
decreased cell proliferation
|
J:184918
|
increased apoptosis
|
J:184918
|
Wnt1tm1.1Mze/Wnt1tm1.1Mze Gt(ROSA)26Sortm14(CAG-tdTomato)Hze/Gt(ROSA)26Sor+ Shhtm1(EGFP/cre)Cjt/Shh+
(involves: 129S6/SvEvTac * C57BL/6N)
|
premature neuronal precursor differentiation
|
J:194842
|
Wnt2tm1.1(rtTA)Eem/Wnt2tm1.1(rtTA)Eem
(involves: 129X1/SvJ * C57BL/6)
|
decreased mesenchymal cell proliferation involved in lung development
|
J:153098
|
Wnt3tm1Amc/Wnt3tm2Amc Tg(Msx2-cre)5Rem/0
(involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ)
|
increased ectoderm apoptosis
|
J:81795
|
Wnt4tm1Amc/Wnt4tm1Amc
(involves: 129S1/Sv)
|
abnormal female germ cell morphology
|
J:52554
|
abnormal oogenesis
|
J:52554
|
decreased oocyte number
|
J:52554
|
oocyte degeneration
|
J:52554
|
Wnt4tm1Amc/Wnt4tm3(EGFP/cre)Amc
(involves: 129S1/Sv * C57BL/6J)
|
abnormal oogenesis
|
J:203797
|
decreased oocyte number
|
J:203797
|
Wnt5atm1Amc/Wnt5atm1.1Krvl H2az2Tg(Wnt1-cre)11Rth/H2az2+
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * CBA/J)
|
abnormal axon extension
|
J:196291
|
increased neuron apoptosis
|
J:196291
|
Wnt5atm1Amc/Wnt5atm1Amc
(involves: 129S7/SvEvBrd)
|
abnormal primordial germ cell migration
|
J:179805
|
decreased primordial germ cell number
|
J:179805
|
increased primordial germ cell apoptosis
|
J:179805
|
Wnt6tm1Akis/Wnt6tm1Akis
(involves: 129P2/OlaHsd * CD-1 * NMRI)
|
abnormal cell cycle
|
J:193969
|
decreased cell proliferation
|
J:193969
|
Wnt7apx-J/Wnt7apx-J
(C57BL/6J-Wnt7apx-J/GrsrJ)
|
abnormal sperm motility
|
J:188477
|
Wnt7btm1Eem/Wnt7btm1Eem
(either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6))
|
abnormal mesenchymal cell proliferation involved in lung development
|
J:79395
|
Wnt7btm2Amc/Wnt7btm2.1Amc Edil3Tg(Sox2-cre)1Amc/Edil3+
(involves: 129X1/SvJ * C57BL/6 * CBA)
|
abnormal kidney cell proliferation
|
J:142685
|
decreased kidney cell proliferation
|
J:142685
|
decreased mesenchymal cell proliferation involved in lung development
|
J:134483
|
increased kidney apoptosis
|
J:142685
|
Wrntm1Led/Wrn+
(involves: 129S6/SvEvTac * Black Swiss)
|
cardiac interstitial fibrosis
|
J:106446
|
Wrntm1Led/Wrntm1Led
(B6.129S6(BKSW)-Wrntm1Led)
|
cardiac interstitial fibrosis
|
J:106446
|
increased cellular sensitivity to oxidative stress
|
J:106446
|
oxidative stress
|
J:106446
|
Wrntm1Led/Wrntm1Led
(involves: 129S6/SvEvTac * Black Swiss)
|
cardiac interstitial fibrosis
|
J:106446
|
Wrntm1Lgu/Wrntm1Lgu
(involves: BALB/c)
|
abnormal cell physiology
|
J:61567
|
Wsb1tm1.1Jszh/Wsb1tm1.1Jszh Ubcem1(cre/ERT2)Smoc/Ubc+
(involves: C57BL/6J * C57BL/6N)
|
abnormal myofibroblast differentiation
|
J:358004
|
decreased apoptosis
|
J:358004
|
Wt/Wt
(Not Specified)
|
abnormal mitosis
|
J:122950
|
Wt1tm1.1Lahe/Wt1+
(involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL)
|
abnormal mesangial cell morphology
|
J:154995
|
Wt1tm1Asc/Wt1+
(involves: 129S7/SvEvBrd * C57BL/6)
|
decreased germ cell number
|
J:71149
|
Wt1tm1Asc/Wt1tm1Asc
(involves: 129S7/SvEvBrd * C57BL/6J)
|
decreased germ cell number
|
J:71149
|
Wt1tm1Jae/Wt1tm1Jae
(involves: 129S4/SvJae * C57BL/6)
|
increased metanephric mesenchyme apoptosis
|
J:14317
|
Wt1tm1Jae/Wt1tm1Jae
(involves: 129S4/SvJae * C57BL/6 * MF1)
|
increased splenocyte apoptosis
|
J:56651
|
Wt1tm1Mlh/Wt1+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal mesangial cell morphology
|
J:135449
|
increased mesangial cell number
|
J:135449
|
Wt1tm1Mlh/Wt1+
(129P2/OlaHsd-Wt1tm1Mlh)
|
abnormal mesangial cell morphology
|
J:135449
|
increased mesangial cell number
|
J:135449
|
Wt1tm1Mlh/Wt1+
(involves: 129P2/OlaHsd * C57BL/6 * MF1)
|
abnormal mesangial cell morphology
|
J:135449
|
increased mesangial cell number
|
J:135449
|
Wt1tm1Vih/Wt1+
(involves: 129S7/SvEvBrd * C57BL/6)
|
impaired granulosa cell differentiation
|
J:204518
|
Wt1tm2Hst/Wt1+
(chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac)
|
abnormal mesangial cell morphology
|
J:53585
|
azoospermia
|
J:103489
|
increased mesangial cell number
|
J:53585
|
Wwoxtm1Ria/Wwoxtm1Ria
(involves: 129X1/SvJ * C57BL/6J)
|
abnormal osteoblast differentiation
|
J:138140
|
Wwp1tm1Lmat/Wwp1tm1Lmat
(involves: 129S1/Sv * C57BL/6 * CBA)
|
enhanced osteoblast differentiation
|
J:190204
|
Wwtr1tm1.1Eno/Wwtr1+ Yap1tm1.1Eno/Yap1tm1.1Eno Tg(Myh6-cre)2182Mds/0
(involves: 129S/SvEv * FVB/N)
|
increased cardiomyocyte apoptosis
|
J:200670
|
Wwtr1tm1.2Hmc/Wwtr1tm1.2Hmc Yap1tm1.2Hmc/Yap1+ Tg(Myh11-cre,-EGFP)2Mik/0
(involves: 129 * C57BL/6 * DBA/2)
|
abnormal mitochondrial physiology
|
J:344215
|
Wwtr1tm1Whun/Wwtr1tm1Whun
(either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6))
|
abnormal renal tubule epithelial cell primary cilium morphology
|
J:119488
|
Xbp1tm1.2Geno/Xbp1tm1.2Geno
(involves: 129S2/SvPas * C57BL/6)
|
decreased cell proliferation
|
J:211440
|
Xbp1tm1Glm/Xbp1tm1Glm
(involves: 129S2/SvPas)
|
decreased hepatocyte proliferation
|
J:59916
|
increased hepatocyte apoptosis
|
J:59916
|
Xbp1tm2Glm/Xbp1tm2Glm Tg(Defa6-icre)1Rsb/0
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal autophagy
|
J:206084
|
Xbp1tm2Glm/Xbp1tm2Glm Tg(Vil1-cre)997Gum/0
(involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL)
|
abnormal cell migration
|
J:188627
|
abnormal endoplasmic reticulum morphology
|
J:188627
|
abnormal small intestine goblet cell morphology
|
J:188627
|
Xbp1tm2Glm/Xbp1tm2Glm Tg(Vil1-cre)997Gum/0
(involves: 129S6/SvEvTac * C57BL/6 * SJL)
|
abnormal autophagy
|
J:206084
|
Xbp1tm2Glm/Xbp1tm2Glm Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2)
|
abnormal autophagy
|
J:206084
|
Xbp1tm3Glm/Xbp1tm3Glm Tg(Vil1-cre/ERT2)23Syr/0
(involves: 129S6/SvEvTac * C57BL/6 * DBA/2)
|
increased apoptosis
|
J:188627
|
Xdhtm1.1Takni/Xdhtm1.1Takni
(involves: C57BL/6)
|
oxidative stress
|
J:281671
|
Xdhtm1Fink/Xdhtm1Fink
(involves: 129X1/SvJ * C57BL/6J)
|
oxidative stress
|
J:166326
|
Xdhtm2.1Takni/Xdhtm2.1Takni
(involves: C57BL/6)
|
cellular phenotype
|
J:281671
|
Xiaptm1Hs/Xiaptm1Hs
(B6.129P2-Xiaptm1Hs)
|
increased sensitivity to induced cell death
|
J:138979
|
Xicb/Xicc Xiaf2/Xiaf2+
(involves: 129X1/SvJ * C57BL/6J * CAST/Ei * CBA/J)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:85407
|
Xirp1tm1Jl/Xirp1+
(involves: 129)
|
cardiac interstitial fibrosis
|
J:132079
|
Xirp1tm1Jl/Xirp1tm1Jl
(involves: 129)
|
cardiac interstitial fibrosis
|
J:132079
|
Xirp2tm1Jl/Xirp2tm1Jl
(B6.129-Xirp2tm1Jl)
|
increased cardiomyocyte apoptosis
|
J:158491
|
Xisttm1.1Nbd/Xist+
(involves: 129 * C57BL/6)
|
cellular phenotype
|
J:85305
|
Xisttm1Jae/Xist+
(involves: 129S4/SvJae)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:95871
|
Xisttm1Nbd/Xisttm1Nbd
(involves: 129 * C57BL/6)
|
abnormal imprinting
|
J:68080
|
Xisttm2.1Jae/Xist+
(involves: 129)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:95871
|
Xisttm2.1Nbd/Xist+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:85305
|
Xisttm2Nbd/Xist+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:85305
|
Xisttm2Sado/Y
(involves: 129S1/Sv * 129X1/SvJ)
|
cellular phenotype
|
J:99399
|
Xisttm2Sado/Xist+
(involves: 129S1/Sv * 129X1/SvJ)
|
cellular phenotype
|
J:99399
|
Xisttm3Nbd/Xist+
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:85305
|
Xisttm5.2Nbd/Xist+
(involves: 129P2/OlaHsd)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:171502
|
Xisttm5Sado/Xist+
(involves: 129S4/SvJae)
|
abnormal imprinting
|
J:142921
|
Xkr8tm1.2Osa/Xkr8tm1.2Osa
(B6.Cg-Xkr8tm1.2Osa)
|
abnormal male germ cell apoptosis
|
J:293092
|
decreased male germ cell number
|
J:293092
|
increased male germ cell apoptosis
|
J:293092
|
oligozoospermia
|
J:293092
|
Xlch/?
(C57BL/6J-Xlch)
|
cardiac interstitial fibrosis
|
J:136798
|
Xpatm1Gvh/Xpatm1Hvs
(involves: 129P2/OlaHsd * C57BL/6J)
|
decreased cellular sensitivity to ultraviolet irradiation
|
J:179808
|
Xpatm1Gvh/Xpatm1Hvs Tg(CAG-cre)13Miya/0
(involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:179808
|
Xpatm1Hvs/Xpatm1Hvs
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal cell physiology
|
J:112689
|
Xpatm1Hvs/Xpatm1Hvs
(involves: 129P2/OlaHsd * C57BL/6J)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:122013
|
Xpatm1Hvs/Xpatm1Hvs
(involves: 129P2/OlaHsd)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:145759
|
Xpatm1Tnka/Xpatm1Tnka
(involves: C57BL/6 * CBA)
|
abnormal base-excision repair
|
J:28709
|
increased cellular sensitivity to ultraviolet irradiation
|
J:35054,
J:28709
|
Xpctm1Brd/Xpctm1Brd
(involves: 129S7/SvEvBrd * C57BL)
|
abnormal cell physiology
|
J:28708
|
Xpctm1Ecf/Xpctm1Ecf
(involves: 129)
|
increased cellular sensitivity to ultraviolet irradiation
|
J:80212
|
oxidative stress
|
J:70397
|
Xpo4em1Gshan/Xpo4+
(involves: C57BL/6J)
|
absent sperm head
|
J:330082
|
asthenozoospermia
|
J:330082
|
coiled sperm flagellum
|
J:330082
|
decreased sperm progressive motility
|
J:330082
|
increased cell death
|
J:330082
|
oligozoospermia
|
J:330082
|
teratozoospermia
|
J:330082
|
Xrcc1tm1Pmc/Xrcc1tm1Pmc Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * C57BL/6 * SJL)
|
abnormal DNA repair
|
J:145730,
J:152528
|
abnormal neuron differentiation
|
J:152528
|
cellular phenotype
|
J:226703
|
increased neuron apoptosis
|
J:152528
|
Xrcc1tm1Pmc/Xrcc1tm1Pmc Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * FVB/N)
|
abnormal DNA repair
|
J:170077
|
Xrcc1tm1Pmc/Xrcc1tm1Pmc Trp53tm1Tyj/Trp53tm1Tyj Tg(Nes-cre)1Kln/0
(involves: 129S1/Sv * 129S2/SvPas * C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:152528
|
Xrcc2tm1Jtk/Xrcc2tm1Jtk
(involves: 129S/SvEv * C57BL/6)
|
chromosomal instability
|
J:66529
|
increased apoptosis
|
J:66529
|
increased cellular sensitivity to gamma-irradiation
|
J:66529
|
increased embryonic tissue cell apoptosis
|
J:66529
|
increased neuron apoptosis
|
J:66529
|
Xrcc2tm1Pmc/Xrcc2tm1Pmc
(involves: 129S1/Sv * C57BL/6)
|
increased apoptosis
|
J:111068
|
Xrcc4tm1Fwa/Xrcc4tm1Fwa
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:110848
|
abnormal DNA repair
|
J:120145
|
increased cellular sensitivity to gamma-irradiation
|
J:120145
|
increased neuron apoptosis
|
J:110848
|
spontaneous chromosome breakage
|
J:120145
|
Xrcc5tm1Dbr/Xrcc5+
(involves: 129S6/SvEvTac * C57BL/6)
|
chromosome breakage
|
J:80467
|
Xrcc5tm1Dbr/Xrcc5+ Lig4tm1Fwa/Lig4+
(involves: 129S6/SvEvTac * C57BL/6)
|
chromosome breakage
|
J:80467
|
Xrcc5tm1Dbr/Xrcc5tm1Dbr
(involves: 129S1/Sv * C57BL/6)
|
increased retina apoptosis
|
J:86825
|
Xrcc5tm1Dbr/Xrcc5tm1Dbr
(involves: 129S6/SvEvTac * C57BL/6)
|
chromosome breakage
|
J:80467
|
Xrcc5tm1Dbr/Xrcc5tm1Dbr
(Not Specified)
|
increased neuron apoptosis
|
J:110848
|
Xrcc5tm1Dbr/Xrcc5tm1Dbr Lig4tm1Fwa/Lig4tm1Fwa
(involves: 129S6/SvEvTac * C57BL/6)
|
chromosome breakage
|
J:80467
|
Xrcc5tm1Nus/Xrcc5tm1Nus
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal double-strand DNA break repair
|
J:108657
|
increased cellular sensitivity to ionizing radiation
|
J:108657
|
Xrcc6tm1Fwa/Xrcc6tm1Fwa
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal cell physiology
|
J:44361
|
decreased cell proliferation
|
J:44361
|
early cellular replicative senescence
|
J:44361
|
increased cellular sensitivity to gamma-irradiation
|
J:44361
|
Xrcc6tm1Fwa/Xrcc6tm1Fwa
(involves: 129S6/SvEvTac)
|
abnormal cell physiology
|
J:110848
|
increased neuron apoptosis
|
J:110848
|
Xrcc6tm1Gcl/Xrcc6tm1Gcl
(involves: 129S1/Sv * C57BL/6)
|
abnormal cell physiology
|
J:108657
|
increased cellular sensitivity to ionizing radiation
|
J:108657
|
XydsqM. macedonius/XydsqM. macedonius
(involves: C57BL/6J * M. macedonius)
|
abnormal male meiosis
|
J:94029
|
Xylt1npo/Xylt1npo
(involves: C57BL/6J * FVB/NJ)
|
abnormal osteoclast differentiation
|
J:205339
|
X/Y(IsXPAR;Y)Ei
(involves: LT/SvEi)
|
abnormal chromosomal synapsis
|
J:2277
|
X/Yaa
(B6.SB-Yaa/J)
|
increased splenocyte proliferation
|
J:127600
|
Yap1tm1.1Dupa/Yap1tm1.1Dupa Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
(involves: 129P2/OlaHsd * C57BL/6 * DBA)
|
increased hepatocyte apoptosis
|
J:162628
|
increased hepatocyte proliferation
|
J:162628
|
Yap1tm1.1Dupa/Yap1tm1.1Dupa Tg(Vil1-cre)997Gum/0
(involves: 129P2/OlaHsd * C57BL/6J * SJL)
|
abnormal enterocyte proliferation
|
J:165471
|
increased enterocyte apoptosis
|
J:165471
|
Yap1tm1.1Fcam/Yap1tm1.1Fcam Tg(KRT14-cre)1Amc/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
decreased cell proliferation
|
J:171057
|
increased cell proliferation
|
J:171057
|
Yap1tm1.1Fcam/Yap1tm2.1Fcam Tg(KRT14-cre)1Amc/0
(involves: 129S4/SvJae * C57BL/6 * CBA)
|
decreased cell proliferation
|
J:171057
|
Yars1tm1.1Rwb/Yars1tm1.1Rwb
(involves: C57BL/6N * FVB/N)
|
abnormal DNA-templated transcription
|
J:310162
|
Ybx1tm1Ley/Ybx1tm1Ley
(either: 129X1/SvJ-Ybx1tm1Ley or (involves: 129X1/SvJ * C57BL/6))
|
abnormal redox activity
|
J:99099
|
decreased fibroblast proliferation
|
J:99099
|
early cellular replicative senescence
|
J:99099
|
Ybx1tm1Tuch/Ybx1tm1Tuch
(involves: 129S/SvEv * C57BL/6)
|
abnormal cell morphology
|
J:117725
|
decreased fibroblast proliferation
|
J:117725
|
Ybx2tm1Nbh/Ybx2tm1Nbh
(involves: 129S7/SvEvBrd)
|
abnormal zona pellucida morphology
|
J:97817
|
azoospermia
|
J:97817
|
decreased oocyte number
|
J:97817
|
increased male germ cell apoptosis
|
J:97817
|
Ybx3tm1Ley/Ybx3tm1Ley
(involves: 129X1/SvJ * C57BL/6)
|
oligozoospermia
|
J:115970
|
Yif1btm1.2Ics/Yif1btm1.2Ics
(involves: 129 * 129S2/SvPas * C57BL/6J)
|
abnormal Golgi apparatus morphology
|
J:284998
|
abnormal Golgi cisterna morphology
|
J:284998
|
abnormal Golgi vesicle transport
|
J:284998
|
Yipf6M1Btlr/Y
(C57BL/6J-Yipf6M1Btlr/Mmucd)
|
abnormal intestinal goblet cell morphology
|
J:187584
|
Yipf6M1Btlr/Yipf6M1Btlr
(C57BL/6J-Yipf6M1Btlr/Mmucd)
|
abnormal intestinal goblet cell morphology
|
J:187584
|
Yme1l1tm1Tlan/Yme1l1tm1Tlan Tg(Myh6-cre)2182Mds/0
(involves: C57BL/6 * C57BL/6NCrl * FVB/N)
|
abnormal mitochondrial physiology
|
J:229455
|
abnormal myocardial fiber mitochondrial morphology
|
J:229455
|
decreased mitochondrial size
|
J:229455
|
increased cardiac muscle cell glucose uptake
|
J:229455
|
Ythdc1tm1.1Jw/Ythdc1tm1.2Jw Tg(Ddx4-cre)1Dcas/0
(involves: 129S4/SvJae * C57BL/6 * FVB)
|
abnormal DNA-templated transcription
|
J:262823
|
abnormal oocyte morphology
|
J:262823
|
absent oocytes
|
J:262823
|
azoospermia
|
J:262823
|
decreased spermatogonia number
|
J:262823
|
Ythdc2em1Chhe/Ythdc2em1Chhe
(involves: BALB/c * C57BL/6J)
|
abnormal female meiosis
|
J:243743
|
arrest of male meiosis
|
J:243743
|
azoospermia
|
J:243743
|
decreased germ cell number
|
J:243743
|
increased male germ cell apoptosis
|
J:243743
|
Ythdc2em1Embrp/Ythdc2em1Embrp
(involves: C57BL/6J)
|
abnormal female meiosis
|
J:243742
|
arrest of male meiosis
|
J:243742
|
azoospermia
|
J:243742
|
decreased oocyte number
|
J:243742
|
increased male germ cell apoptosis
|
J:243742
|
Ythdc2em1Sky/Ythdc2em1Sky
(involves: C57BL/6J * CBA)
|
arrest of male meiosis
|
J:256276
|
Ythdc2em2Chhe/Ythdc2em2Chhe
(involves: BALB/c * C57BL/6J)
|
azoospermia
|
J:243743
|
decreased germ cell number
|
J:243743
|
Ythdc2em2Embrp/Ythdc2em2Embrp
(involves: C57BL/6J)
|
abnormal female meiosis
|
J:243742
|
arrest of male meiosis
|
J:243742
|
azoospermia
|
J:243742
|
decreased oocyte number
|
J:243742
|
increased male germ cell apoptosis
|
J:243742
|
Ythdc2ketu/Ythdc2ketu
(involves: C57BL/6J * FVB/NJ)
|
arrest of male meiosis
|
J:256276
|
azoospermia
|
J:256276
|
increased male germ cell apoptosis
|
J:256276
|
Ythdf1em1Chhe/Ythdf1em1Chhe
(B6.Cg-Ythdf1em1Chhe)
|
abnormal translation
|
J:267186
|
Ythdf1tm1.1Sjj/Ythdf1tm1.1Sjj Tg(Atoh1-cre/Esr1*)14Fsh/0
(involves: FVB/N)
|
abnormal axon guidance
|
J:276416
|
Ythdf2em2Jhha/Ythdf2em2Jhha
(involves: BALB/c * C57BL/6)
|
oligozoospermia
|
J:299108
|
Ythdf2tm1.1Doca/Ythdf2tm1.1Doca Tg(Zp3-cre)3Mrt/0
(involves: FVB/N)
|
maternal effect
|
J:243747
|
Ythdf2tm1c(KOMP)Wtsi/Ythdf2tm1c(KOMP)Wtsi Stra8em1(GFP/cre)Smoc/Stra8+
(involves: C57BL/6N)
|
asthenozoospermia
|
J:324152
|
decreased sperm progressive motility
|
J:324152
|
increased male germ cell apoptosis
|
J:324152
|
oligozoospermia
|
J:324152
|
teratozoospermia
|
J:324152
|
Ythdf2tm1c(KOMP)Wtsi/Ythdf2tm1c(KOMP)Wtsi Tg(Ddx4-cre)1Dcas/0
(involves: C57BL/6N * FVB)
|
asthenozoospermia
|
J:324152
|
decreased sperm progressive motility
|
J:324152
|
increased male germ cell apoptosis
|
J:324152
|
oligozoospermia
|
J:324152
|
teratozoospermia
|
J:324152
|
Ywhaetm1Awb/Ywhaetm1Awb
(either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss))
|
decreased neuronal migration
|
J:84075
|
Ywhaetm1Awb/Ywhaetm1Awb
(involves: 129S6/SvEvTac)
|
abnormal cell cycle
|
J:192860
|
decreased fetal cardiomyocyte proliferation
|
J:192860
|
decreased mitotic index
|
J:192860
|
YwhaqGt(RRR746)Byg/Ywhaq+
(involves: 129P2/OlaHsd * C57BL/6)
|
increased cardiomyocyte apoptosis
|
J:118280
|
YwhazGt(OST432062)Lex/YwhazGt(OST432062)Lex
(either: B6.129S5-YwhazGt(OST432062)Lex or C.129S5-YwhazGt(OST432062)Lex or (involves: 129S5/SvEvBrd * 129T2/SvEmsWehi)))
|
abnormal neuronal migration
|
J:217297
|
Yy1tm1Yshi/Yy1tm2Yshi
(involves: 129S4/SvJae)
|
decreased cell proliferation
|
J:108369
|
Yy1tm2.1Yshi/Yy1tm2.1Yshi Shhtm1(EGFP/cre)Cjt/Shh+
(involves: 129S4/SvJae * C57BL/6J)
|
impaired myofibroblast differentiation
|
J:239777
|
increased lung apoptosis
|
J:239777
|
Zap70m1Saka/Zap70m1Saka
(involves: BALB/c)
|
decreased T cell proliferation
|
J:154166,
J:86607
|
Zap70m1Saka/Zap70m1Saka Tg(DO11.10)10Dlo/0
(involves: BALB/c * C3H * C57BL/6)
|
decreased T cell proliferation
|
J:86607
|
Zap70tm1.1Mmal/Zap70tm1.1Mmal Tg(TcrLCMV)327Sdz/0
(involves: 129P2/OlaHsd * BALB/cJ * C57BL/6 * DBA/2)
|
abnormal T cell proliferation
|
J:71099
|
Zap70tm2.1Weis/Zap70tm2.1Weis
(C.129S4-Zap70tm2.1Weis)
|
decreased T cell proliferation
|
J:154166
|
Zar1em1Hyfn/Zar1em1Hyfn
(involves: C57BL/6 * ICR)
|
abnormal female meiosis
|
J:282460
|
impaired polar body extrusion
|
J:282460
|
maternal effect
|
J:282460
|
Zar1em1Hyfn/Zar1em1Hyfn Zar1lem1Hyfn/Zar1lem1Hyfn
(involves: C57BL/6 * ICR)
|
abnormal female meiosis
|
J:282460
|
abnormal female meiosis I arrest
|
J:282460
|
aneuploidy
|
J:282460
|
impaired polar body extrusion
|
J:282460
|
maternal effect
|
J:282460
|
Zar1tm1Zuk/Zar1tm1Zuk
(involves: 129S6/SvEvTac * 129S7/SvEvBrd)
|
maternal effect
|
J:81447
|
Zar1tm1Zuk/Zar1tm1Zuk
(involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6J)
|
maternal effect
|
J:81447
|
Zar1lem1Hyfn/Zar1lem1Hyfn
(involves: C57BL/6 * ICR)
|
abnormal female meiosis
|
J:282460
|
impaired polar body extrusion
|
J:282460
|
Zbed3tm1.1Lil/Zbed3tm1.1Lil
(Not Specified)
|
maternal effect
|
J:296111
|
Zbp1tm1.1Jreh/Zbp1tm1.1Jreh
(involves: C57BL/6 * C57BL/6N)
|
decreased cell death
|
J:252669
|
Zbtb7ctm1Mwhu/Zbtb7ctm1Mwhu
(involves: 129S4/SvJae * C57BL/6)
|
decreased cell proliferation
|
J:181490
|
Zbtb16lu/Zbtb16lu
(B6.C3-Zbtb16Lu)
|
azoospermia
|
J:89934
|
decreased male germ cell number
|
J:89934
|
Zbtb16lu/Zbtb16lu
(Not Specified)
|
azoospermia
|
J:5206
|
Zbtb16tm1Geno/Zbtb16tm1Geno
(Not Specified)
|
abnormal DNA methylation
|
J:199097
|
abnormal epigenetic regulation of gene expression
|
J:199097
|
abnormal male germ cell apoptosis
|
J:199097
|
Zbtb16tm1Ppp/Zbtb16tm1Ppp
(involves: 129S1/Sv)
|
abnormal spermatogonia proliferation
|
J:91129
|
asthenozoospermia
|
J:91129
|
decreased spermatogonia number
|
J:91129
|
increased male germ cell apoptosis
|
J:91129
|
oligozoospermia
|
J:91129
|
Zbtb16tm2Geno/Zbtb16tm2Geno
(Not Specified)
|
abnormal DNA methylation
|
J:199097
|
Zbtb17tm1Cksn/Zbtb17tm1Cksn Commd10Tg(Vav1-icre)A2Kio/Commd10+
(B6.Cg-Zbtb17tm1Cksn Commd10Tg(Vav1-icre)A2Kio)
|
increased T cell apoptosis
|
J:170508
|
Zbtb17tm1Cksn/Zbtb17tm1Cksn Krt14tm1(cre)Wbm/Krt14+
(involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ)
|
increased keratinocyte proliferation
|
J:123966
|
Zbtb17tm1Elr/Zbtb17tm1Elr
(involves: 129X1/SvJ * C57BL/6)
|
decreased cell proliferation
|
J:86265
|
increased apoptosis
|
J:86265
|
Zbtb18tm1.1Nda/Zbtb18tm1.1Nda Tg(Nes-cre)1Kln/0
(involves: C57BL/6 * SJL)
|
abnormal neuron differentiation
|
J:184434
|
abnormal neuronal migration
|
J:184434
|
abnormal radial glial cell morphology
|
J:184434
|
increased neuron apoptosis
|
J:184434
|
Zbtb18tm1Haok/Zbtb18tm1Haok
(involves: 129/Sv * C57BL/6)
|
increased neuron apoptosis
|
J:150768
|
Zbtb18tm1Haok/Zbtb18tm1Haok
(involves: 129)
|
abnormal axon extension
|
J:196306
|
abnormal neuron differentiation
|
J:196306
|
abnormal neuronal migration
|
J:196306
|
abnormal neuronal precursor proliferation
|
J:196306
|
increased neuron apoptosis
|
J:196306
|
Zbtb18tm2.1Haok/Zbtb18tm2.1Haok
(involves: 129)
|
abnormal neuron differentiation
|
J:196306
|
abnormal neuronal migration
|
J:196306
|
Zbtb20Tg(PDGFB-APPSwInd)20Lms/0
(involves: C57BL/6 * DBA/2)
|
abnormal neuron differentiation
|
J:121330
|
Zbtb32Gt(IST12443F7)Tigm/Zbtb32Gt(IST12443F7)Tigm
(involves: C57BL/6N)
|
abnormal cell physiology
|
J:200274
|
Zbtb32tm1Iho/Zbtb32tm1Iho
(involves: BALB/c)
|
increased T cell proliferation
|
J:94944
|
Zbtb32tm1Iho/Zbtb32tm1Iho
(involves: C57BL/6)
|
increased T cell proliferation
|
J:94944
|
Zbtb32tm2Ppp/Zbtb32tm2Ppp
(involves: 129S1/Sv)
|
increased T cell proliferation
|
J:95119
|
Zbtb40em1Clab/Zbtb40em1Clab
(C57BL/6J-Zbtb40em1Clab)
|
impaired osteoblast differentiation
|
J:293133
|
Zc3h4em1(IMPC)Mbp/Zc3h4em1(IMPC)Mbp
(C57BL/6NCrl-Zc3h4em1(IMPC)Mbp/Mmucd)
|
absent inner cell mass proliferation
|
J:279207,
J:301719
|
cellular phenotype
|
J:301719
|
decreased cell proliferation
|
J:301719
|
increased embryonic tissue cell apoptosis
|
J:301719
|
Zc3h12atm1Aki/Zc3h12atm1Aki
(involves: 129X1/SvJ * C57BL/6)
|
abnormal cell physiology
|
J:147868
|
Zc3h12dtm1Tom/Zc3h12dtm1Tom
(B6.Cg-Zc3h12dtm1Tom)
|
increased T cell proliferation
|
J:209383
|
Zc3hav1tm1Aki/Zc3hav1tm1Aki
(involves: 129 * C57BL/6)
|
abnormal cell physiology
|
J:198791
|
Zc3hc1tm1.2Jduy/Zc3hc1tm1.2Jduy
(B6.129S6(Cg)-Zc3hc1tm1.2Jduy)
|
abnormal apoptosis
|
J:185584
|
abnormal chromosomal synapsis
|
J:185584
|
abnormal double-strand DNA break repair
|
J:185584
|
abnormal female meiosis
|
J:185584
|
abnormal meiosis
|
J:185584
|
abnormal spermatocyte morphology
|
J:185584
|
abnormal synaptonemal complex
|
J:185584
|
arrest of male meiosis
|
J:185584
|
azoospermia
|
J:185584
|
decreased male germ cell number
|
J:185584
|
decreased oocyte number
|
J:185584
|
decreased spermatid number
|
J:185584
|
increased female germ cell apoptosis
|
J:185584
|
increased male germ cell apoptosis
|
J:185584
|
Zcchc8em1Sgao/Zcchc8em1Sgao
(involves: C57BL/6 * DBA/2)
|
abnormal cell differentiation
|
J:297024
|
abnormal female meiosis
|
J:297024
|
abnormal mitosis
|
J:297024
|
abnormal oocyte morphology
|
J:297024
|
decreased cell proliferation
|
J:297024
|
maternal effect
|
J:297024
|
oligozoospermia
|
J:297024
|
Zcchc17tm1Pou/Zcchc17tm1Pou
(involves: 129 * C57BL/6J)
|
cellular phenotype
|
J:233160
|
Zcchc17tm2Pou/Zcchc17tm2Pou
(involves: 129 * C57BL/6J)
|
abnormal cell differentiation
|
J:233160
|
early cellular replicative senescence
|
J:233160
|
oxidative stress
|
J:233160
|
Zcchc17tm3Pou/Zcchc17tm3Pou
(involves: 129 * C57BL/6J)
|
cellular phenotype
|
J:233160
|
Zcwpw1em1(IMPC)Tcp/Zcwpw1em1(IMPC)Tcp
(C57BL/6N-Zcwpw1em1(IMPC)Tcp)
|
abnormal chromosomal synapsis
|
J:296124
|
abnormal double-strand DNA break repair
|
J:296124
|
absent chiasmata formation
|
J:296124
|
arrest of male meiosis
|
J:296124
|
azoospermia
|
J:296124
|
Zcwpw1em1Kliu/Zcwpw1em1Kliu
(C57BL/6-Zcwpw1em1Kliu)
|
abnormal chromosomal synapsis
|
J:278517
|
abnormal double-strand DNA break repair
|
J:278517
|
abnormal female meiosis
|
J:278517
|
absent oocytes
|
J:278517
|
arrest of male meiosis
|
J:278517
|
azoospermia
|
J:278517
|
Zdbf2em1Dhbh/Zdbf2+
(involves: C57BL/6J * DBA/2J)
|
abnormal DNA methylation
|
J:261327
|
Zdhhc13Gt(AC0492)Wtsi/Zdhhc13Gt(AC0492)Wtsi
(FVB.129P2-Zdhhc13Gt(AC0492)Wtsi)
|
increased neuron apoptosis
|
J:191129
|
Zdhhc17Gt(RRJ233)Byg/Zdhhc17Gt(RRJ233)Byg
(FVB.129P2-Zdhhc17Gt(RRJ233)Byg)
|
increased neuron apoptosis
|
J:175800
|
Zdhhc19em1Cya/Zdhhc19em1Cya
(C57BL/6N-Zdhhc19em1Cya/Cya)
|
abnormal sperm head morphology
|
J:316357
|
asthenozoospermia
|
J:316357
|
coiled sperm flagellum
|
J:316357
|
kinked sperm flagellum
|
J:316357
|
Zdhhc19em1Mngx/Zdhhc19em1Mngx
(involves: C57BL/6)
|
abnormal sperm flagellum morphology
|
J:323394
|
abnormal sperm head morphology
|
J:323394
|
asthenozoospermia
|
J:323394
|
decreased sperm progressive motility
|
J:323394
|
increased male germ cell apoptosis
|
J:323394
|
oligozoospermia
|
J:323394
|
teratozoospermia
|
J:323394
|
Zeb1m1Btlr/Zeb1m1Btlr
(involves: C57BL/6J)
|
decreased B cell proliferation
|
J:185495
|
Zeb2tm1.1Yhi/Zeb2tm1.1Yhi Tg(Dct-lacZ)A12Jkn/0 Tg(Tyr-cre)1Lru/Y
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA * DBA/2)
|
abnormal melanoblast migration
|
J:211299
|
Zeb2tm1.2Yhi/Zeb2tm1.2Yhi
(involves: 129S1/Sv * 129X1/SvJ * CD-1)
|
abnormal cranial neural crest cell migration
|
J:82084
|
abnormal neural crest cell delamination
|
J:82084
|
Zfand2aGt(XM071)Byg/Zfand2aGt(XM071)Byg
(involves: 129P2/OlaHsd)
|
abnormal cell physiology
|
J:112707
|
Zfand5Gt(ROSA)72Sor/Zfand5Gt(ROSA)72Sor
(involves: 129S4/SvJaeSor)
|
decreased fibroblast cell migration
|
J:117491
|
Zfattm2.1Sawa/Zfattm2.1Sawa Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * C57BL/6JJcl * C57BL/6NCrSlc * DBA/2)
|
decreased T cell proliferation
|
J:187164
|
increased T cell apoptosis
|
J:187164
|
Zfp24tm1Jifu/Zfp24tm1Jifu
(involves: 129X1/SvJ * C57BL/6J)
|
absent inner cell mass proliferation
|
J:156988
|
Zfp36tm1Pjb/Zfp36tm1Pjb
(B6.Cg-Zfp36tm1Pjb)
|
increased cellular sensitivity to oxidative stress
|
J:214114
|
oxidative stress
|
J:214114
|
Zfp36l1tm1.1Tnr/Zfp36l1tm1.1Tnr Zfp36l2tm1.1Tnr/Zfp36l2tm1.1Tnr Tg(CD2-icre)4Kio/0
(involves: C57BL/6 * C57BL/10 * CBA/Ca * SJL)
|
increased cell proliferation
|
J:162388
|
Zfp36l1tm1Pjb/Zfp36l1tm1Pjb
(Not Specified)
|
abnormal apoptosis
|
J:91579
|
decreased cell proliferation
|
J:91579
|
Zfp36l3tm1Pjb/Zfp36l3+
(involves: C57BL/6 * C57BL/6NTac)
|
abnormal dosage compensation, by inactivation of X chromosome
|
J:230794
|
paternal imprinting
|
J:230794
|
Zfp42Gt(XB238)Byg/Zfp42Gt(XB238)Byg
(involves: 129P2/OlaHsd * C57BL/6)
|
abnormal DNA methylation
|
J:169234
|
abnormal imprinting
|
J:169234
|
Zfp42tm1.1Log/Zfp42tm1.1Log
(involves: 129S1/Sv * C57BL/6 * C57BL/6J)
|
abnormal sperm head morphology
|
J:175380
|
decreased male germ cell number
|
J:175380
|
kinked sperm flagellum
|
J:175380
|
oligozoospermia
|
J:175380
|
Zfp57tm1.1Xjli/Zfp57tm1.1Xjli
(either: 129S6/SvEvTac-Zfp57tm1.1Xjli or (involves: 129S6/SvEvTac * Black Swiss * FVB/N))
|
abnormal imprinting
|
J:143283
|
maternal effect
|
J:143283
|
Zfp106tm1a(KOMP)Wtsi/Zfp106tm1a(KOMP)Wtsi
(involves: C57BL/6Brd * C57BL/6Dnk * C57BL/6N)
|
abnormal mitochondrial ATP synthesis coupled electron transport
|
J:229162
|
abnormal mitochondrial physiology
|
J:229162
|
abnormal redox activity
|
J:229162
|
increased spinal cord apoptosis
|
J:229162
|
Zfp110tm1Mpin/Zfp110tm1Mpin
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6NCrl)
|
decreased retina apoptosis
|
J:66924
|
Zfp131tm1.1Mytk/Zfp131tm1.1Mytk Tg(Cd4-cre)1Cwi/0
(involves: C57BL/6 * C57BL/6N * DBA/2)
|
decreased T cell proliferation
|
J:271921
|
Zfp131tm1.1Mytk/Zfp131tm1.2Mytk Tg(Lck-cre)1Jtak/0
(involves: C57BL/6N * FVB/N)
|
decreased T cell proliferation
|
J:271921
|
Zfp148tm1Kii/Zfp148+
(Not Specified)
|
abnormal male germ cell apoptosis
|
J:81445
|
Zfp277tm1Aiwa/Zfp277tm1Aiwa
(involves: 129S1/Sv * 129X1/SvJ)
|
early cellular replicative senescence
|
J:198334
|
Zfp281tm1.1Jlwa/Zfp281tm1.1Jlwa
(involves: 129S1/Sv)
|
abnormal cell differentiation
|
J:190201
|
Zfp296tm1Miya/Zfp296tm1Miya
(B6.129P2-Zfp296tm1Miya)
|
abnormal DNA methylation
|
J:255491
|
abnormal primordial germ cell morphology
|
J:255491
|
decreased germ cell number
|
J:255491
|
decreased male germ cell number
|
J:255491
|
decreased oocyte number
|
J:255491
|
decreased primordial germ cell number
|
J:255491
|
decreased primordial germ cell proliferation
|
J:255491
|
oligozoospermia
|
J:255491
|
Zfp422em1Mode/Zfp422em1Mode Myf5tm3(cre)Sor/Myf5+
(involves: 129S4/SvJaeSor * C57BL/6J)
|
abnormal myoblast differentiation
|
J:297035
|
Zfp422em1Mode/Zfp422em1Mode Pax7tm1(cre/ERT2)Gaka/Pax7+
(involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl)
|
abnormal myoblast differentiation
|
J:297035
|
Zfp423tm1Reed/Zfp423tm1Reed
(involves: 129 * C57BL/6)
|
abnormal cerebellar granule cell precursor proliferation
|
J:122606
|
Zfp451em1Ssli/Zfp451em1Ssli
(involves: C57BL/6J)
|
abnormal fibroblast physiology
|
J:351311
|
increased fibroblast cell migration
|
J:351311
|
Zfp467tm1.1(KOMP)Vlcg/Zfp467tm1.1(KOMP)Vlcg
(B6(Cg)-Zfp467tm1.1(KOMP)Vlcg)
|
enhanced osteoblast differentiation
|
J:302865
|
Zfp503tm1.1Lif/Zfp503tm1.1Lif
(involves: 129 * C57BL/6)
|
abnormal neuronal migration
|
J:286635
|
Zfp516Gt(A044B05)Wrst/Zfp516Gt(A044B05)Wrst
(involves: 129S2/SvPas * C57BL/6J)
|
abnormal brown fat cell differentiation
|
J:218161
|
disorganized mitochondrial cristae
|
J:218161
|
Zfp521tm1Nohk/Zfp521tm1Nohk
(B6J.Cg-Zfp521tm1Nohk)
|
impaired neuron differentiation
|
J:214267
|
Zfp541em1Fcw/Zfp541em1Fcw
(Not Specified)
|
abnormal double-strand DNA break repair
|
J:338159
|
abnormal male meiosis
|
J:338159
|
abnormal spermatocyte morphology
|
J:338159
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:338159
|
arrest of male meiosis
|
J:338159
|
azoospermia
|
J:338159
|
increased male germ cell apoptosis
|
J:338159
|
Zfp541em1Osb/Zfp541em1Osb Tg(CAG-EGFP,Acr-EGFP)2Osb/0
(involves: 129S2/SvPas * C57BL/6NSlc)
|
abnormal male meiosis
|
J:306305
|
abnormal synaptonemal complex
|
J:306305
|
abnormal X-Y chromosome synapsis during male meiosis
|
J:306305
|
arrest of male meiosis
|
J:306305
|
decreased round spermatid number
|
J:306305
|
increased primordial germ cell apoptosis
|
J:306305
|
Zfp574em1Btlr/Zfp574em1Btlr
(C57BL/6J-Zfp574em1Btlr)
|
decreased B cell proliferation
|
J:354285
|
increased B cell apoptosis
|
J:354285
|
Zfp628em1Frei/Zfp628+
(involves: CD-1)
|
decreased male germ cell number
|
J:292511
|
Zfp628em1Frei/Zfp628em1Frei
(involves: CD-1)
|
abnormal acrosome morphology
|
J:292511
|
azoospermia
|
J:292511
|
increased male germ cell apoptosis
|
J:292511
|
multinucleated giant male germ cells
|
J:292511
|
Zfp640Gt(ROSA)81Sor/Zfp640Gt(ROSA)81Sor
(involves: 129S4/SvJaeSor)
|
decreased fibroblast cell migration
|
J:117491
|
Zfp708em1Dame/Zfp708em1Dame
(Not Specified)
|
maternal imprinting
|
J:284126
|
Zfp750tm1b(EUCOMM)Wtsi/Zfp750tm1b(EUCOMM)Wtsi
(B6(Cg)-Zfp750tm1b(EUCOMM)Wtsi)
|
abnormal epidermal stem cell proliferation
|
J:335426
|
abnormal keratinocyte differentiation
|
J:335426
|
Zfp809Gt(F065A07)Wrst/Zfp809Gt(F065A07)Wrst
(involves: 129S2/SvPas)
|
abnormal cell physiology
|
J:219938
|
Zfp809tm1a(KOMP)Wtsi/Zfp809tm1a(KOMP)Wtsi
(involves: C57BL/6N)
|
abnormal cell physiology
|
J:219938
|
Zfp809tm1c(KOMP)Wtsi/Zfp809tm1c(KOMP)Wtsi Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
(involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6N)
|
abnormal cell physiology
|
J:219938
|
Zfp830tm1Cota/Zfp830tm1Cota
(either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6N))
|
abnormal cell cycle
|
J:99352
|
absent inner cell mass proliferation
|
J:99352
|
absent trophectoderm cell proliferation
|
J:99352
|
decreased inner cell mass proliferation
|
J:99352
|
Zfp830tm2.1Cota/Zfp830tm2.2Cota Gt(ROSA)26Sortm2(cre/ERT2)Brn/?
(involves: 129P2/OlaHsd * 129S2/SvPas * BALB/c * C57BL/6)
|
decreased cell proliferation
|
J:171647
|
early cellular replicative senescence
|
J:171647
|
Zfp949tm1Htno/Zfp949tm1Htno
(involves: 129S1/Sv * 129X1/SvJ)
|
decreased cell proliferation
|
J:259302
|
increased embryonic tissue cell apoptosis
|
J:259302
|
Zfp950Gt(ROSA)76Sor/Zfp950Gt(ROSA)76Sor
(involves: 129S4/SvJaeSor)
|
abnormal cell migration
|
J:117491
|
Zfp998em1Aiwsk/Del(13Zfp997-Vmn2r-ps103)1Aiwsk
(involves: C57BL/6J)
|
abnormal epigenetic regulation of gene expression
|
J:282526
|
cellular phenotype
|
J:282526
|
Zfpm1tm1.1Esv/Zfpm1tm1.1Esv
(involves: 129S6/SvEvTac * C57BL/6)
|
abnormal megakaryocyte differentiation
|
J:156475
|
Zfpm1tm1Sho/Zfpm1tm1Sho
(either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6))
|
abnormal megakaryocyte differentiation
|
J:47281
|
Zfpm1tm2Sho/Zfpm1tm2Sho
(either: (involves: 129S1/Sv) or (involves: 129S1/Sv * C57BL/6))
|
abnormal megakaryocyte differentiation
|
J:47281
|
Zfpm2tm1Sho/Zfpm2tm2Sho Tg(Myh6-cre)2182Mds/0
(involves: 129S1/Sv * 129S7/SvEvBrd)
|
increased cardiomyocyte apoptosis
|
J:150452
|
Zfpm2tm1Sho/Zfpm2tm2Sho Tg(Tnnt2-rtTA,tetO-cre)1Wtp/0
(involves: 129S1/Sv * 129S7/SvEvBrd)
|
increased cardiomyocyte apoptosis
|
J:150452
|
Zfxtm1Dcp/Y
(involves: 129S4/SvJae * BALB/c)
|
decreased primordial germ cell number
|
J:41131
|
oligozoospermia
|
J:41131
|
Zfxtm1Dcp/Zfx+
(involves: 129S4/SvJae * BALB/c)
|
decreased germ cell number
|
J:41131
|
decreased oocyte number
|
J:41131
|
Zfxtm1Dcp/Zfxtm1Dcp
(involves: 129S4/SvJae * BALB/c)
|
decreased oocyte number
|
J:41131
|
decreased primordial germ cell number
|
J:41131
|
Zfyve16tm2a(KOMP)Wtsi/Zfyve16tm2a(KOMP)Wtsi
(C57BL/6N-Zfyve16tm2a(KOMP)Wtsi)
|
decreased B cell proliferation
|
J:302014
|
Zfyve26tm1.1Cahb/Zfyve26tm1.1Cahb
(involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6)
|
abnormal lysosome morphology
|
J:223127
|
abnormal lysosome physiology
|
J:223127
|
delayed axon extension
|
J:223127
|
Zglp1tm1Eem/Zglp1tm1Eem
(involves: 129S1/Sv * 129X1/SvJ)
|
abnormal spermatogonia proliferation
|
J:116977
|
decreased male germ cell number
|
J:116977
|
increased testis apoptosis
|
J:116977
|
oligozoospermia
|
J:116977
|
Zic2Ku/Zic2Ku
(C3.CAnNCrl-Zic2Ku)
|
increased ectoderm apoptosis
|
J:138862
|
Zic3tm1Bca/Y
(involves: 129S7/SvEvBrd)
|
abnormal motile primary cilium morphology
|
J:194989
|
Zmat3em1Ast/Zmat3em1Ast
(either: (involves: C57BL/6) or (involves: 129 * C57BL/6))
|
cellular phenotype
|
J:271583
|
Zmiz1tm1Zsu/Zmiz1tm1Zsu
(involves: 129S6/SvEvTac * C57BL/6J)
|
decreased cell proliferation
|
J:128915
|
Zmpste24tm1Otin/Zmpste24tm1Otin
(involves: 129P2/Ola * C57BL/6)
|
cardiac interstitial fibrosis
|
J:76209
|
increased hair follicle apoptosis
|
J:76209
|
Zmpste24tm1Sgy/Zmpste24tm1Sgy
(involves: 129S4/SvJae * C57BL/6)
|
abnormal cell nucleus morphology
|
J:95274,
J:106473
|
abnormal cell physiology
|
J:79501
|
Zmym3em1Hncs/Zmym3em1Hncs
(involves: C57BL/6J * CBA)
|
arrest of male meiosis
|
J:324172
|
decreased elongated spermatid number
|
J:324172
|
decreased round spermatid number
|
J:324172
|
decreased spermatid number
|
J:324172
|
increased male germ cell apoptosis
|
J:324172
|
oligozoospermia
|
J:324172
|
Zmynd10tm1(KOMP)Wtsi/Zmynd10tm1(KOMP)Wtsi
(involves: C57BL/6J * C57BL/6N)
|
abnormal brain ependyma motile cilium morphology
|
J:261915
|
abnormal brain ependyma motile cilium physiology
|
J:261915
|
abnormal respiratory motile cilium morphology
|
J:261915
|
Zp1tm1Dean/Zp1tm1Dean
(involves: 129S1/Sv * 129X1/SvJ * CF-1)
|
abnormal zona pellucida morphology
|
J:56560
|
thin zona pellucida
|
J:56560
|
Zp2tm1Dean/Zp2tm1Dean
(involves: 129S1/Sv * 129X1/SvJ * CF-1)
|
thin zona pellucida
|
J:67817
|
Zp3tm1Dean/Zp3tm1Dean
(involves: 129S4/SvJae * C57BL/6J)
|
absent zona pellucida
|
J:36772
|
Zp3tm1Dean/Zp3tm1Dean Tg(ZP3)7812Dean/?
(involves: 129S4/SvJae * C57BL/6J * FVB/N)
|
thin zona pellucida
|
J:93482
|
Zp3tm1Pmw/Zp3+
(involves: 129S1/Sv * C57BL/6J)
|
thin zona pellucida
|
J:39483
|
Zp3tm1Pmw/Zp3tm1Pmw
(involves: 129S1/Sv * C57BL/6J)
|
abnormal oocyte morphology
|
J:47519
|
absent zona pellucida
|
J:47519,
J:33254
|
Zpbp2tm1Zuk/Zpbp2tm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
teratozoospermia
|
J:126661
|
Zpbptm1Zuk/Zpbp+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
teratozoospermia
|
J:126661
|
Zpbptm1Zuk/Zpbp+ Zpbp2tm1Zuk/Zpbp2+
(involves: 129S7/SvEvBrd * C57BL/6J)
|
teratozoospermia
|
J:126661
|
Zpbptm1Zuk/Zpbp+ Zpbp2tm1Zuk/Zpbp2tm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
teratozoospermia
|
J:126661
|
Zpbptm1Zuk/Zpbptm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal acrosome morphology
|
J:126661
|
abnormal sperm flagellum morphology
|
J:126661
|
abnormal sperm nucleus morphology
|
J:126661
|
abnormal spermatid morphology
|
J:126661
|
absent acrosome
|
J:126661
|
asthenozoospermia
|
J:126661
|
coiled sperm flagellum
|
J:126661
|
detached sperm flagellum
|
J:126661
|
globozoospermia
|
J:126661
|
teratozoospermia
|
J:126661
|
Zpbptm1Zuk/Zpbptm1Zuk Zpbp2tm1Zuk/Zpbp2tm1Zuk
(involves: 129S7/SvEvBrd * C57BL/6J)
|
abnormal acrosome morphology
|
J:126661
|
abnormal sperm flagellum morphology
|
J:126661
|
abnormal sperm nucleus morphology
|
J:126661
|
abnormal spermatid morphology
|
J:126661
|
absent acrosome
|
J:126661
|
asthenozoospermia
|
J:126661
|
coiled sperm flagellum
|
J:126661
|
detached sperm flagellum
|
J:126661
|
globozoospermia
|
J:126661
|
teratozoospermia
|
J:126661
|
Zpr1tm1Rjd/Zpr1tm1Rjd
(involves: 129S6/SvEvTac * C57BL/6J)
|
abnormal Cajal body morphology
|
J:97582
|
abnormal inner cell mass apoptosis
|
J:97582
|
decreased inner cell mass proliferation
|
J:97582
|
Zranb1em1Shios/Zranb1em1Shios
(involves: C57BL/6)
|
abnormal colon goblet cell morphology
|
J:333468
|
Zscan5btm1Thama/Zscan5btm1Thama
(involves: C57BL/6)
|
increased chromosomal stability
|
J:289891
|
Zscan10Gt(285B6)1.1Cmhd/Zscan10Gt(285B6)1.1Cmhd
(involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N)
|
maternal effect
|
J:221010
|
Zswim7em1Mjn/Zswim7em1Mjn
(involves: C57BL/6J * CBA/J)
|
abnormal chromosomal synapsis
|
J:268570
|
increased ovary apoptosis
|
J:268570
|
Zyxtm1Mbk/Zyxtm1Mbk
(B6.129X1-Zyxtm1Mbk)
|
abnormal cell adhesion
|
J:107919
|
abnormal cell morphology
|
J:107919
|
impaired fibroblast cell migration
|
J:107919
|
increased fibroblast cell migration
|
J:107919
|