Excel File Text File All mouse models of autosomal genetic disease with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      2-aminoadipic 2-oxoadipic aciduria Dhtkd1em1Hpr/Dhtkd1em1Hpr involves: C57BL/6N * FVB/N J:256227 View
3-methylglutaconic aciduria type 3 Opa3m1Votr/Opa3m1Votr involves: C3H * C57BL/6JCrl J:181670, J:188346 View
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Serac1em1Bcgen/Serac1em1Bcgen C57BL/6N-Serac1em1Bcgen J:326672 View
17-beta hydroxysteroid dehydrogenase 3 deficiency Hsd17b3tm1.2Mpo/Hsd17b3tm1.2Mpo involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl J:301756 View
aceruloplasminemia Cptm1Yos/Cptm1Yos C.129P2-Cptm1Yos J:142713 View
aceruloplasminemia Cptm1Hrs/Cptm1Hrs involves: 129X1/SvJ * Black Swiss J:57730, J:71807 View
aceruloplasminemia Cptm1Hrs/Cptm1Hrs
Hephsla/Y
involves: 129X1/SvJ * C57BL/6 J:92620 View
acheiropody Lmbr1tm1Kng/Lmbr1tm1Kng involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J J:72166 View
achondrogenesis type IA Trip11m1Mawa/Trip11m1Mawa C57BL/6J-Trip11m1Mawa J:163656 View
achondrogenesis type IA Tg(EIIa-cre)C5379Lmgd/?
Trip11tm1.2Psmi/Trip11tm1.2Psmi
involves: 129/Sv * C57BL/6 * FVB/N J:253969 View
achondrogenesis type IA Trip11tm1.1Psmi/Trip11tm1.2Psmi
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/?
Tg(Col2a1-cre)1Bhr/?
involves: 129/Sv * C57BL/6 * SJL/J J:253969 View
achondrogenesis type II Col2a1tm1Prc/Col2a1tm1Prc involves: 129 J:117910 View
achromatopsia 2 Cnga3cpfl5/Cnga3cpfl5 B6.RHJ-Cnga3cpfl5/BocJ J:187090 View
achromatopsia 2 Cnga3tm1Biel/Cnga3tm1Biel involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:56020 View
achromatopsia 2 Cnga3cpfl5/Cnga3cpfl5 involves: RHJ/LeJ J:187090 View
achromatopsia 3 Cngb3cpfl10/Cngb3cpfl10 involves: 129S6/SvEvTac * C57BL/6J J:269211 View
achromatopsia 3 Cngb3tm1Dgen/Cngb3tm1Dgen involves: C57BL/6 J:154304 View
achromatopsia 7 Atf6tm1.1Rjk/Atf6tm1.1Rjk involves: C57BL/6 * C57BL/6J J:231780 View
acromesomelic dysplasia, Grebe type Gdf5Bp-5J/Gdf5+ C57BL/6J-Gdf5Bp-5J/GrsrJ J:200816 View
acromesomelic dysplasia, Grebe type Gdf5bp-J/Gdf5bp-J
Gdf6tm1Kng/Gdf6tm1Kng
involves: 129S1/Sv * 129X1/SvJ * A/J * C57BL/6J J:83132 View
acromesomelic dysplasia, Hunter-Thompson type Gdf5Bp-5J/Gdf5+ C57BL/6J-Gdf5Bp-5J/GrsrJ J:200816 View
acromesomelic dysplasia, Maroteaux type Npr2pwe/Npr2pwe involves: C3H/HeJ * C57BL/6 * NAW/WI J:188839 View
acromesomelic dysplasia, Maroteaux type Npr2slw/Npr2slw involves: C57BL/6 * DDY J:129973 View
adenine phosphoribosyltransferase deficiency Aprttm1Dwm/Aprttm1Dwm involves: 129P2/OlaHsd * BALB/c J:38450 View
adenine phosphoribosyltransferase deficiency Aprttm1Jat/Aprttm1Jat involves: 129S2/SvPas * Black Swiss J:33255 View
adenine phosphoribosyltransferase deficiency Aprttm1Jat/Aprttm1Jat involves: 129S2/SvPas * C57BL/6J J:33255 View
adult hypophosphatasia AlplBAP023/AlplBAP023 C3HeB/FeJ-AlplBAP023 J:183993 View
adult hypophosphatasia AlplMhdabap020/AlplMhdabap020 C3HeB/FeJ-AlplMhdabap020/Ieg J:183993 View
adult hypophosphatasia AlplMhdabap26/AlplMhdabap26 C3HeB/FeJ-AlplMhdabap26 J:183993 View
adult hypophosphatasia AlplMhdabap27/AlplMhdabap27 C3HeB/FeJ-AlplMhdabap27 J:183993 View
adult hypophosphatasia AlplMhdabap32/AlplMhdabap32 C3HeB/FeJ-AlplMhdabap32 J:183993 View
adult hypophosphatasia Alpltm1Sor/Alpltm1Sor either: (involves: 129S7/SvEvBrd-Alpltm1Sor) or (involves: 129S7/SvEvBrd * C57BL/6) J:28394 View
adult hypophosphatasia Alpltm2.1Jlm/Alpl+ involves: 129S4/SvJaeSor * C57BL/6 J:237759 View
adult hypophosphatasia AlplHpp/AlplHpp involves: BALB/cAnN * C3H/HeH J:122319 View
adult hypophosphatasia AlplHpp/Alpl+ involves: BALB/cAnN * C3H/HeH J:122319 View
adult-onset autosomal dominant demyelinating leukodystrophy Tg(Lmnb1)1Yfu/0 involves: C57BL/6J J:197168 View
adult-onset autosomal dominant demyelinating leukodystrophy Tg(Plp1-Lmnb1)#Yfu/0 involves: FVB J:197168 View
adult-onset autosomal dominant demyelinating leukodystrophy Tg(Plp1-LMNB1)1108Qsp/0 involves: FVB/N J:226169 View
advanced sleep phase syndrome 1 Per2M1Btlr/Per2M1Btlr C57BL/6J-Per2M1Btlr J:264638 View
advanced sleep phase syndrome 1 Tg(PER2*S662G)867Ljp/0 involves: C57BL/6 J:126404 View
age related macular degeneration 4 Cfhtm1Mbo/Cfhtm1Mbo B6.129-Cfhtm1Mbo J:203471 View
age related macular degeneration 12 Cx3cr1tm1Zm/Cx3cr1tm1Zm C.129-Cx3cr1tm1Zm J:127548 View
age related macular degeneration 12 Cx3cr1tm1Zm/Cx3cr1tm1Zm involves: 129 * C57BL/6 J:127548 View
agenesis of the corpus callosum with peripheral neuropathy Slc12a6tm1Garo/Slc12a6tm1Garo
Tg(Syn1-cre)671Jxm/0
involves: 129 * C57BL/6 * CBA J:183239 View
agenesis of the corpus callosum with peripheral neuropathy Slc12a6tm1Dlp/Slc12a6tm1Dlp involves: 129 * C57BL/6J J:79870 View
agenesis of the corpus callosum with peripheral neuropathy Slc12a6tm1Tjj/Slc12a6tm1Tjj involves: 129/Sv * C57BL/6 J:86183 View
Aicardi-Goutieres syndrome Trex1tm1Tld/Trex1tm1Tld involves: 129P2/OlaHsd J:145466 View
Aicardi-Goutieres syndrome Adarem1Stsn/Adartm1.1Phs
Meox2tm1(cre)Sor/Meox2+
involves: 129S1/Sv * 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J J:308678 View
Aicardi-Goutieres syndrome Adarem1Stsn/Adartm1Olds involves: 129S/SvEv * C57BL/6J J:308678 View
alacrima, achalasia, and impaired intellectual development syndrome Gmppatm1d(EUCOMM)Wtsi/Gmppatm1d(EUCOMM)Wtsi involves: C57BL/6N J:305791 View
Alexander disease Gfaptm3Mes/Gfap+ involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N J:114689 View
Alexander disease Gfaptm2Mes/Gfap+ involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N J:114689 View
Alexander disease Gfaptm2Mes/Gfap+
Tg(GFAP)10Mes/0
involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N J:114689 View
Alexander disease Gfaptm2Mes/Gfap+
Tg(GFAP)10Mes/0
involves: 129S7/SvEvBrd * FVB/N J:146191 View
Alexander disease Tg(Gfap-GFAP*R239H)60TMIke/0 involves: C57BL/6J J:139349, J:138318 View
Alexander disease Tg(GFAP)10Mes/0 involves: FVB/N J:99256 View
Alexander disease Tg(GFAP)7Mes/0 involves: FVB/N J:99256 View
alopecia universalis Hrrh-8J/Hrrh-8J B10.D2/nSnJ-Hrrh-8J J:50909 View
alopecia universalis Hrrhsl/Hrrhsl involves: BALB/c J:98859 View
alopecia universalis Hrrh-Chr/Hrrh-Chr Not Specified J:53633 View
alpha thalassemia-X-linked intellectual disability syndrome Atrxtm1Rjg/Y
Foxg1tm1(cre)Skm/Foxg1+
involves: 129P2/OlaHsd * C57BL/6 * FVB/N J:95953 View
alpha thalassemia-X-linked intellectual disability syndrome Atrxtm1Rjg/Y
Tg(Pax6-cre,GFP)2Pgr/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N J:145002 View
alpha thalassemia-X-linked intellectual disability syndrome Atrxtm1Rjg/Y
Tg(Nes-cre)2472Pick/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N J:95953 View
alpha-2-plasmin inhibitor deficiency Serpinf2tm1Hrl/Serpinf2tm1Hrl involves: 129X1/SvJ * C57BL/6J J:54047, J:55243 View
Alstrom syndrome Alms1m2Btlr/Alms1m2Btlr C57BL/6J-Alms1m2Btlr J:264648 View
Alstrom syndrome Alms1m3Btlr/Alms1m3Btlr C57BL/6J-Alms1m3Btlr J:264649 View
Alstrom syndrome Alms1tvrm102/Alms1tvrm102 C57BL/6J-Alms1tvrm102/Pjn J:243745 View
Alstrom syndrome Alms1Gt(XH152)Byg/Alms1Gt(XH152)Byg involves: 129P2/OlaHsd * C57BL/6J J:100403 View
Alstrom syndrome Alms1L2131X/Alms1L2131X involves: C57BL/6 * NOD J:118221 View
Alstrom syndrome Alms1foz/Alms1foz involves: NOD J:107058 View
Alzheimer's disease 3 Tg(APP695)3Dbo/0
Tg(PSEN1dE9)S9Dbo/0
B6.Cg-Tg(APP695)3Dbo Tg(PSEN1dE9)S9Dbo/Mmjax J:157228 View
Alzheimer's disease 3 Tg(APPswe,PSEN1dE9)85Dbo/0 B6;C3-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax J:113199 View
Alzheimer's disease 3 Psen1tm1Lpr/Psen1tm1Lpr
Tg(Thy1-APPSL)28Lpr/0
either: 129/Sv or (involves: 129/Sv * C57BL/6) J:93770 View
Alzheimer's disease 3 Psen1tm1Mpm/Psen1tm1Pcw involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 J:91277 View
Alzheimer's disease 3 Tg(APP695)3Dbo/0
Tg(PSEN1dE9)S9Dbo/0
involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J J:123534 View
Alzheimer's disease 3 Psen1tm1Mpm/Psen1tm1Mpm involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:51950 View
Alzheimer's disease 3 Psen1tm1Tak/Psen1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:108326 View
Alzheimer's disease 3 Tg(PSEN1H163R)G9Btla/0 involves: 129S4/SvJae J:58050 View
Alzheimer's disease 3 Psen1tm1Shn/Psen1tm1Shn involves: 129S7/SvEvBrd * C57BL/6 J:40365 View
Alzheimer's disease 3 Tg(APP695)3Dbo/0
Tg(PSEN1)5Dbo/0
involves: C3H/HeJ * C57BL/6J J:43788 View
Alzheimer's disease 3 Tg(APP695)3Dbo/0
Tg(PSEN1dE9)S9Dbo/0
involves: C3H/HeJ * C57BL/6J J:123534 View
Alzheimer's disease 3 Tg(APPswe,PSEN1dE9)85Dbo/0 involves: C3H/HeJ * C57BL/6J J:87691, J:113200 View
Alzheimer's disease 3 Tg(PSEN1dE9)S9Dbo/0 involves: C3H/HeJ * C57BL/6J J:104147 View
Alzheimer's disease 3 Tg(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0 involves: C57BL/6 * SJL J:112949 View
Alzheimer's disease 3 Psen1tm1Vln/Psen1tm1Vln
Tg(Thy1-cre)1Vln/0
involves: FVB/N J:87229 View
amelogenesis imperfecta hypomaturation type 2A2 Mmp20tm1Jdb/Mmp20tm1Jdb involves: 129P2/OlaHsd * C57BL/6 J:80925 View
amelogenesis imperfecta hypomaturation type 2A3 Wdr72tm1a(KOMP)Wtsi/Wdr72tm1a(KOMP)Wtsi involves: C57BL/6N J:215636 View
amelogenesis imperfecta type 1B Enamtm1.1Jcch/Enamtm1.1Jcch involves: C57BL/6 J:223123 View
amelogenesis imperfecta type 1B Enamtm1.1Jcch/Enam+ involves: C57BL/6 J:223123 View
amelogenesis imperfecta type 1B EnamRgsc395/Enam+ involves: C57BL/6JJcl * DBA/2J J:96349 View
amelogenesis imperfecta type 1B EnamRgsc514/Enam+ involves: C57BL/6JJcl * DBA/2J J:96349 View
amelogenesis imperfecta type 1B EnamRgsc521/EnamRgsc521 involves: C57BL/6JJcl * DBA/2J J:96349 View
amelogenesis imperfecta type 1B EnamRgsc521/Enam+ involves: C57BL/6JJcl * DBA/2J J:96349 View
amelogenesis imperfecta type 3C Reltem1Jpsi/Reltem1Jpsi C57BL/6-Reltem1Jpsi J:279949 View
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome Trp63tm1Cmis/Trp63+ involves: 129P2/OlaHsd * C57BL/6 J:191121 View
antithrombin III deficiency Serpinc1tm1Dwr/Serpinc1tm1Dwr involves: 129S1/Sv * 129X1/SvJ J:115658 View
arrhythmogenic right ventricular dysplasia 2 Ryr2tm1Slh/Ryr2+ involves: 129S7/SvEvBrd * C57BL/6 J:111780 View
arrhythmogenic right ventricular dysplasia 8 Dsptm1Efu/Dsptm1Efu
Myl2tm1(cre)Krc/Myl2+
involves: 129 * 129S4/SvJae * C57BL/6 J:205990 View
arrhythmogenic right ventricular dysplasia 10 Dsg2tm1d(EUCOMM)Wtsi/Dsg2tm1d(EUCOMM)Wtsi involves: C57BL/6J * C57BL/6N J:235770 View
arrhythmogenic right ventricular dysplasia 12 Tg(Myh6-JUP*)1Dpju/0 FVB/N-Tg(Myh6-JUP*)1Dpju J:235770 View
arrhythmogenic right ventricular dysplasia 12 Juptm1.1Shou/Juptm1.1Shou
Tg(Myh6-cre)2182Mds/0
involves: 129 * C57BL/6J J:177567 View
arrhythmogenic right ventricular dysplasia 12 Juptm1Ruiz/Jup+
Tg(Myh6-Jup*)1Ajm/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N J:192719 View
arrhythmogenic right ventricular dysplasia 12 Juptm1.1Glr/Juptm1.1Glr
A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
involves: 129S6/SvEvTac * C57BL/6 * FVB/N * SJL J:170618 View
arrhythmogenic right ventricular dysplasia 12 Tg(Myh6-Jup*)1Ajm/0 involves: FVB/N J:192719 View
asphyxiating thoracic dystrophy 2 Ift80Gt(AN0245)Wtsi/Ift80Gt(AN0245)Wtsi involves: 129P2/OlaHsd J:169236 View
asphyxiating thoracic dystrophy 3 Dync2h1b2b414Clo/Dync2h1b2b414Clo C57BL/6J-Dync2h1b2b414Clo J:175213 View
ataxia telangiectasia Atmtm1Pmc/Atmtm1Pmc B6.Cg-Atmtm1Pmc J:222034 View
ataxia telangiectasia Atmtm1Awb/Atmtm1Awb either: 129S6/SvEvTac-Atmtm1Awb or (involves: 129S6/SvEvTac * NIH Black Swiss) J:34193, J:57115 View
ataxia telangiectasia Aptxtm1Pmc/Aptxtm1Pmc
Atmtm2.1Mfgc/Atmtm2.1Mfgc
involves: 129 * C57BL/6 J:316365 View
ataxia telangiectasia Atmtm1Bal/Atmtm1Bal involves: 129S4/SvJae J:42324, J:44190 View
ataxia telangiectasia Atmtm1Fwa/Atmtm1Fwa involves: 129S4/SvJae * C57BL/6 J:61201 View
ataxia telangiectasia Atmtm1.1Mmpl/Atmtm1.1Mmpl involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J J:226414 View
ataxia telangiectasia Atmtm1Led/Atmtm1Led involves: 129S6/SvEvTac * Black Swiss J:36561 View
ataxia telangiectasia Atmtm1Mfl/Atmtm1Mfl involves: 129T2/SvEms * C57BL/6J J:69726 View
ataxia telangiectasia Atmtm1Pmc/Atmtm1Pmc involves: 129X1/SvJ * C57BL/6 J:47752 View
Athabaskan brainstem dysgenesis syndrome Hoxa1tm3.1Mrc/Hoxa1tm3.1Mrc involves: 129S1/Sv * 129X1/SvJ J:178887 View
atransferrinemia Trfhpx/Trfhpx BALB/cJ-Trfhpx J:64456, J:8936 View
atransferrinemia Trfhpx/Trf+ BALB/cJ-Trfhpx J:64456, J:8936 View
atrial heart septal defect 2 Gata4tm1Grg/Gata4+ involves: 129 * C57BL/6 J:185124 View
atrial heart septal defect 7 Nkx2-5tm2.1Mwc/Nkx2-5+ B6J.Cg-Nkx2-5tm2.1Mwc/Mwc J:239808 View
atrial heart septal defect 7 Nkx2-5tm3.1Mwc/Nkx2-5+ B6J.Cg-Nkx2-5tm3.1Mwc/Mwc J:239808 View
atrichia with papular lesions Hrrh-8J/Hrrh-8J B10.D2/nSnJ-Hrrh-8J J:50909 View
atrichia with papular lesions Hrrhsl/Hrrhsl involves: BALB/c J:98859 View
autoimmune lymphoproliferative syndrome type 2B Casp8tm1Raz/Casp8tm1Raz
Tg(Lck-cre)548Jxm/0
involves: 129P2/OlaHsd * C57BL/6 * CBA J:107455 View
autosomal dominant auditory neuropathy 1 Tg(CAG-Diap3)924Lesp/0 FVB/NJ-Tg(CAG-Diap3)924Lesp J:193237 View
autosomal dominant auditory neuropathy 1 Tg(CAG-Diaph3)771Lesp/0 FVB/NJ-Tg(CAG-Diaph3)771Lesp J:193237 View
autosomal dominant congenital deafness with onychodystrophy Atp6v1b2tm1Yoyu/Atp6v1b2tm1Yoyu involves: C57BL/6 J:278514 View
autosomal dominant congenital deafness with onychodystrophy Atp6v1b2tm1Yoyu/Atp6v1b2+ involves: C57BL/6 J:278514 View
autosomal dominant familial periodic fever Tnfrsf1atm1Rsie/Tnfrsf1a+ B6.Cg-Tnfrsf1atm1Rsie J:160543 View
autosomal dominant familial periodic fever Tnfrsf1atm2.1Rsie/Tnfrsf1a+ B6.Cg-Tnfrsf1atm2.1Rsie J:160543 View
autosomal dominant familial periodic fever Tnfrsf1atm1Imx/Tnfrsf1atm1Imx involves: 129S7/SvEvBrd * C57BL/6 J:45147 View
autosomal dominant hypocalcemia 1 CasrNuf/Casr+ either: (involves: 102/El * 102/H * C3H/He) or (involves: 102/El * C3H/He * C3H/HeH) J:92612 View
autosomal dominant hypocalcemia 1 CasrNuf/CasrNuf involves: 102/El * C3H/He J:92612 View
autosomal dominant hypocalcemia 2 Gna11em1Mman/Gna11em1Mman C57BL/6NCrl-Gna11em1Mman J:280180 View
autosomal dominant hypocalcemia 2 Gna11em1Mman/Gna11+ C57BL/6NCrl-Gna11em1Mman J:280180 View
autosomal dominant hypophosphatemic rickets Fgf23tm1.1Kew/Fgf23tm1.1Kew B6.129-Fgf23tm1.1Kew J:180061 View
autosomal dominant hypophosphatemic rickets Tg(APOE-FGF23*R176Q)#Ack/0 involves: C57BL/6J * CBA J:93981 View
autosomal dominant hypophosphatemic rickets Fgf23tm1Blan/Fgf23tm1Blan
PhexHyp/Y
Not Specified J:94041 View
autosomal dominant intellectual developmental disorder 7 Dyrk1aem1Kzy/Dyrk1a+ C57BL/6J-Dyrk1aem1Kzy J:259596 View
autosomal dominant intellectual developmental disorder 26 Auts2tm1Mhos/Auts2+ C57BL/6N-Auts2tm1Mhos J:261355 View
autosomal dominant intellectual developmental disorder 38 Eef1a2em#Abb/Eef1a2+ C57BL/6JCrl-Eef1a2em#Abb J:296080 View
autosomal dominant intellectual developmental disorder 39 Myt1lem1Jdd/Myt1l+ C57BL/6-Myt1lem1Jdd/J J:321206 View
autosomal dominant intellectual developmental disorder 39 Myt1lem1Mwer/Myt1l+ involves: C57BL/6N J:326588 View
autosomal dominant keratitis-ichthyosis-deafness syndrome Gjb2tm2.2Kwi/Gjb2+
Tg(Pgk1-cre)1Lni/0
involves: 129/Sv * 129P2/OlaHsd * BALB/c * C57BL/6 J:166732 View
autosomal dominant keratitis-ichthyosis-deafness syndrome Tg(KRT14-rtTA)F42Efu/0
Tg(tetO-GJB2*G45E,-EGFP)#Tww/0
involves: FVB/N * SKH1 J:220589 View
autosomal dominant nocturnal frontal lobe epilepsy 3 Chrnb2tm1.1Cont/Chrnb2tm1.1Cont B6.129-Chrnb2tm1.1Cont J:228269 View
autosomal dominant nocturnal frontal lobe epilepsy 3 Tg(Prnp-tTA)F959Sbp/0
Tg(tetO-Chrnb2*V287L)H3Gica/0
involves: 129S7/SvEvBrd * FVB J:145855 View
autosomal dominant nonsyndromic deafness 9 Cochtm1Mrtn/Cochtm1Mrtn CBACa.129S4-Cochtm1Mrtn J:140594, J:167669 View
autosomal dominant nonsyndromic deafness 12 Tectatm3.1Gpr/Tecta+ involves: 129S/SvEv J:203482 View
autosomal dominant nonsyndromic deafness 12 Tectatm4.1Gpr/Tecta+ involves: 129S/SvEv J:203482 View
autosomal dominant nonsyndromic deafness 12 Tectatm5.1Gpr/Tecta+ involves: 129S/SvEv J:203482 View
autosomal dominant nonsyndromic deafness 12 Tectatm2Gpr/Tecta+ involves: 129S/SvEv * C57BL/6J J:101691 View
autosomal dominant nonsyndromic deafness 13 Col11a2tm1Mne/Col11a2tm1Mne FVB.129-Col11a2tm1Mne J:71948 View
autosomal dominant nonsyndromic deafness 22 Myo6sv/Myo6sv involves: B10.HA/(33NX)Sn * C57BL/6J J:29898 View
autosomal dominant nonsyndromic deafness 22 Myo6em1Bcgen/Myo6+ involves: C57BL/6J * CBA/CaJ J:288210 View
autosomal dominant nonsyndromic deafness 25 Slc17a8tm1Selm/Slc17a8tm1Selm involves: 129/Sv * C57BL/6 J:139493 View
autosomal dominant nonsyndromic deafness 36 Tmc1Mhdabth/Tmc1+ C3HeB/FeJ-Tmc1Mhdabth/Ieg J:86685 View
autosomal dominant nonsyndromic deafness 36 Tmc1dn/Tmc1dn involves: STOCK Grhl3ct * M. m. molossinus J:22445 View
autosomal dominant nonsyndromic deafness 36 Tmc1dn/Tmc1dn STOCK Grhl3ct/J J:236 View
autosomal dominant nonsyndromic deafness 41 P2rx2em1Xzl/P2rx2+ CBA/J-P2rx2em1Xzl J:315007 View
autosomal dominant nonsyndromic deafness 67 Osbpl2em1Cya/Osbpl2em1Cya C57BL/6-Osbpl2em1Cya J:324115 View
autosomal dominant osteopetrosis 2 Clcn7tm1.1Mjec/Clcn7+ involves: 129 * 129S/SvEv * C57BL/6 J:203761 View
autosomal dominant osteopetrosis 2 Clcn7tm1.1Aros/Clcn7tm1.1Aros involves: 129P2/OlaHsd * C57BL/6N J:273179 View
autosomal dominant osteopetrosis 2 Clcn7tm1.1Teti/Clcn7tm1.1Teti involves: 129S2/SvPas * C57BL/6 J:203761 View
autosomal dominant osteopetrosis 2 Clcn7tm1.1Teti/Clcn7+ involves: 129S2/SvPas * C57BL/6 J:203761 View
autosomal dominant osteopetrosis 2 Clcn7tm1.1Teti/Clcn7tm1.1Teti involves: 129S2/SvPas * CD-1 J:203761 View
autosomal dominant osteopetrosis 2 Clcn7tm1.1Mjec/Clcn7+ involves: 129S/SvEv * C57BL/6 * DBA/2J J:203761 View
autosomal dominant osteopetrosis 2 Clcn7tm1.1Mawa/Clcn7+ involves: C57BL/6J * C57BL/6N * CD-1 J:254787 View
autosomal dominant polycystic kidney disease Pkd2tm1.1Gwu/Pkd2tm1.1Gwu
Tg(Vil1-cre)997Gum/0
involves: C57BL/6 * C57BL/6J * SJL J:265516 View
autosomal dominant pseudohypoaldosteronism type 1 Nr3c2tm1Gsc/Nr3c2tm1Gsc involves: 129P2/OlaHsd * C57BL/6 J:77285 View
autosomal recessive Alport syndrome Col4a3tm1Dec/Col4a3tm1Dec 129-Col4a3tm1Dec/J J:158731 View
autosomal recessive Alport syndrome Col4a4bwk/Col4a4bwk 129S1.NON(NZO)-Col4a4bwk/PgnJ J:223185 View
autosomal recessive Alport syndrome Col4a3tm1Dec/Col4a3tm1Dec 129X1/SvJ-Col4a3tm1Dec J:91619 View
autosomal recessive Alport syndrome Col4a4m1Btlr/Col4a4m1Btlr C57BL/6J-Col4a4m1Btlr J:158794, J:170552 View
autosomal recessive Alport syndrome Col4a4bwk/Col4a4bwk D2.NON(NZO)-Col4a4bwk/GrsrJ J:223185 View
autosomal recessive Alport syndrome Col4a3tm1Jhm/Col4a3tm1Jhm
Mmp9tm1Tvu/Mmp9tm1Tvu
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ J:63137 View
autosomal recessive Alport syndrome Col4a3tm1Jhm/Col4a3tm1Jhm involves: 129S1/Sv * 129X1/SvJ J:37017, J:207595 View
autosomal recessive Alport syndrome Col4a3tm1Dec/Col4a3tm1Dec involves: 129X1/SvJ * C57BL/6 J:37963 View
autosomal recessive Alport syndrome Col4a4m1H/Col4a4m1H involves: C3H/HeH * C57BL/6J J:285510 View
autosomal recessive Alport syndrome Col4a4bwk/Col4a4bwk NON;NZO-Col4a4bwk/J J:223185 View
autosomal recessive congenital ichthyosis 1 Tgm1tm1Kfyn/Tgm1tm1Kfyn involves: 129S1/SvImJ * 129X1/SvJ * C57BL/6 J:45653, J:74334 View
autosomal recessive congenital ichthyosis 4B Abca12tm1Shzu/Abca12tm1Shzu B6.129S-Abca12tm1Shzu J:139048 View
autosomal recessive congenital ichthyosis 4B Abca12el12/Abca12el12 involves: 129/Sv * C57BL/6 J:161652 View
autosomal recessive congenital ichthyosis 4B Abca12tm1Lex/Abca12tm1Lex involves: 129S/SvEvBrd * C57BL/6J J:144062 View
autosomal recessive congenital ichthyosis 4B Abca12smsk/Abca12smsk involves: C57BL/6J J:262458 View
autosomal recessive congenital ichthyosis 10 Pnpla1tm1a(KOMP)Wtsi/Pnpla1tm1a(KOMP)Wtsi B6NTac;B6N-Atm1Brd Pnpla1tm1a(KOMP)Wtsi/Ics J:242353 View
autosomal recessive congenital ichthyosis 13 Sdr9c7em1Maak/Sdr9c7em1Maak involves: C57BL/6J J:295441 View
autosomal recessive intellectual developmental disorder Crbntm1.1Jjh/Crbntm1.1Jjh
Tg(Camk2a-cre)T29-1Stl/0
involves: C57BL/6 J:179427 View
autosomal recessive intellectual developmental disorder Crbntm1.2Jjh/Crbntm1.2Jjh involves: C57BL/6 J:259276 View
autosomal recessive isolated ectopia lentis 2 Adamtsl4tvrm267/Adamtsl4tvrm267 C57BL/6J-Adamtsl4tvrm267/Pjn J:226844 View
autosomal recessive limb-girdle muscular dystrophy type 2A Capn3tm1.1Hiso/Capn3tm1.1Hiso B6.129P2-Capn3tm1.1Hiso J:163711 View
autosomal recessive limb-girdle muscular dystrophy type 2A Capn3tm1Jsb/Capn3tm1Jsb either: 129/Sv-Capn3tm1Jsb or (involves: 129/Sv * C57BL/6) J:66862 View
autosomal recessive limb-girdle muscular dystrophy type 2A Capn3Gt(OST141731)Lex/Capn3Gt(OST141731)Lex involves: 129S5/SvEvBrd * C57BL/6 J:91206 View
autosomal recessive limb-girdle muscular dystrophy type 2B Dysfprmd/Dysfprmd A/J J:92838 View
autosomal recessive limb-girdle muscular dystrophy type 2B Dysftm1.1Mdcb/Dysftm1.1Mdcb B6.129P2(Cg)-Dysftm1.1Mdcb J:302056 View
autosomal recessive limb-girdle muscular dystrophy type 2B Dysftm1Kcam/Dysftm1Kcam involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:83126 View
autosomal recessive limb-girdle muscular dystrophy type 2B Dysftm1Meho/Dysftm1Meho involves: 129S4/SvJae * C57BL/6 J:92838 View
autosomal recessive limb-girdle muscular dystrophy type 2B Dysfim/Dysfim involves: SJL J:57764 View
autosomal recessive limb-girdle muscular dystrophy type 2C Sgcgtm1Oza/Sgcgtm1Oza involves: 129S4/SvJae * C57BL/6 J:102780 View
autosomal recessive limb-girdle muscular dystrophy type 2C Sgcgtm1Mcn/Sgcgtm1Mcn involves: 129X1/SvJ * C57BL/6 J:49871, J:57664, J:88456 View
autosomal recessive limb-girdle muscular dystrophy type 2D Sgcatm2Kcam/Sgcatm2Kcam B6.129S6-Sgcatm2Kcam/J J:250485 View
autosomal recessive limb-girdle muscular dystrophy type 2D Sgcatm1Kcam/Sgcatm1Kcam involves: 129S1/Sv * 129X1/SvJ J:49992 View
autosomal recessive limb-girdle muscular dystrophy type 2D Sgcatm1Eeng/Sgcatm1Eeng involves: 129S/SvEv * 129X1/SvJ J:83034 View
autosomal recessive limb-girdle muscular dystrophy type 2E Sgcbtm1Kcam/Sgcbtm1Kcam involves: 129S1/Sv * 129X1/SvJ J:60154 View
autosomal recessive limb-girdle muscular dystrophy type 2E Sgcbtm1Oza/Sgcbtm1Oza involves: 129S4/SvJae * C57BL/6J J:57590 View
autosomal recessive limb-girdle muscular dystrophy type 2F Sgcdtm1Mcn/Sgcdtm1Mcn B6.129-Sgcdtm1Mcn/J J:250485 View
autosomal recessive limb-girdle muscular dystrophy type 2F Sgcdtm1Mcn/Sgcdtm1Mcn involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ J:76730 View
autosomal recessive limb-girdle muscular dystrophy type 2F Sgcdtm1Kcam/Sgcdtm1Kcam involves: 129S1/Sv * 129X1/SvJ J:57107 View
autosomal recessive limb-girdle muscular dystrophy type 2G Tcaptm1Mkc/Tcaptm1Mkc involves: 129 * C57BL/6 J:159687 View
autosomal recessive limb-girdle muscular dystrophy type 2H Trim32Gt(BGA355)Byg/Trim32Gt(BGA355)Byg involves: 129P2/OlaHsd * C57BL/6 J:146155 View
autosomal recessive limb-girdle muscular dystrophy type 2H Trim32tm1Spc/Trim32tm1Spc involves: 129S/SvEvBrd * BALB/cJ * C57BL/6J J:175798 View
autosomal recessive limb-girdle muscular dystrophy type 2I Fkrptm1.1Pg/Fkrptm1.1Pg involves: 129P2/OlaHsd J:285924 View
autosomal recessive limb-girdle muscular dystrophy type 2I Fkrptm1Itl/Fkrptm1Itl involves: 129S6/SvEvTac * C57BL/6N J:164448 View
autosomal recessive limb-girdle muscular dystrophy type 2I Fkrptm1Scbr/Fkrptm1Scbr
Sox1tm1(cre)Take/Sox1+
Tg(CAG-LARGE)126Fmu/0
involves: C57BL/6NCrlj * C57BL/10 * CBA/Ca * CBA/JNCrlj J:207119 View
autosomal recessive limb-girdle muscular dystrophy type 2I Fkrptm1Scbr/Fkrptm1Scbr
Sox1tm1(cre)Take/Sox1+
involves: C57BL/6NCrlj * CBA/JNCrlj J:207119 View
autosomal recessive limb-girdle muscular dystrophy type 2J Ttntm1.1Isrd/Ttntm1.1Isrd involves: 129S2/SvPas * C57BL/6 J:165576 View
autosomal recessive limb-girdle muscular dystrophy type 2J Ttnmdm/Ttnmdm Not Specified J:74611 View
autosomal recessive limb-girdle muscular dystrophy type 2J Ttntm1Her/Ttntm1Her
Tg(Ckmm-cre)5Khn/0
Not Specified J:81993 View
autosomal recessive limb-girdle muscular dystrophy type 2L Ano5tm1Lrk/Ano5tm1Lrk involves: C57BL/6 J:235810 View
autosomal recessive limb-girdle muscular dystrophy type 2P Dag1tm4.1Kcam/Dag1tm4.1Kcam involves: 129S1/Sv * 129X1/SvJ J:169291 View
autosomal recessive limb-girdle muscular dystrophy type 2U Crppaem2Mbp/Crppaem2Mbp
Myf5tm3(cre)Sor/Myf5+
B6.Cg-Myf5tm3(cre)Sor Crppaem2Mbp J:324289 View
autosomal recessive nonsyndromic deafness 1A Gjb2tm1Ugds/Gjb2tm1Ugds
Tg(Otog-cre)1Ugds/0
involves: 129P2/OlaHsd * C57BL/6 J:77823 View
autosomal recessive nonsyndromic deafness 1A Gjb6tm1Kwi/Gjb6tm1Kwi involves: 129P2/OlaHsd * C57BL/6 J:80917 View
autosomal recessive nonsyndromic deafness 1A Gjb2tm1Ugds/Gjb2tm1Ugds
Tg(Sox10-cre)1Wdr/0
involves: 129P2/OlaHsd * C57BL/6 * CBA J:206835 View
autosomal recessive nonsyndromic deafness 1A Gjb6tm1.1Fama/Gjb6tm1.1Fama involves: 129P2/OlaHsd * C57BL/6 * SJL J:166362 View
autosomal recessive nonsyndromic deafness 2 Myo7admbo2/Myo7admbo2 involves: C57BL/6J J:195666 View
autosomal recessive nonsyndromic deafness 3 Myo15atm1.1Jebd/Myo15atm1.1Jebd involves: C57BL/6 * FVB/N J:226820 View
autosomal recessive nonsyndromic deafness 3 Myo15ash2-2J/Myo15ash2-2J involves: STOCK Rb(16.17)7Bnr J:69998 View
autosomal recessive nonsyndromic deafness 7 Tmc1Mhdabth/Tmc1+ C3HeB/FeJ-Tmc1Mhdabth/Ieg J:86685 View
autosomal recessive nonsyndromic deafness 7 Tmc1nice/Tmc1nice involves: C57BL/6 J:181985 View
autosomal recessive nonsyndromic deafness 7 Tmc1stitch/Tmc1stitch involves: C57BL/6 J:181985 View
autosomal recessive nonsyndromic deafness 7 Tmc1baringo/Tmc1baringo involves: C57BL/6 J:181985 View
autosomal recessive nonsyndromic deafness 7 Tmc1dn/Tmc1dn involves: STOCK Grhl3ct * M. m. molossinus J:22445 View
autosomal recessive nonsyndromic deafness 7 Tmc1dn/Tmc1dn STOCK Grhl3ct/J J:236 View
autosomal recessive nonsyndromic deafness 9 Otoftm1Ugds/Otoftm1Ugds involves: 129S2/SvPas * C57BL/6 J:116097 View
autosomal recessive nonsyndromic deafness 9 Otofdeaf5Jcs/Otofdeaf5Jcs STOCK Otofdeaf5Jcs/Kjn J:125960 View
autosomal recessive nonsyndromic deafness 12 Cdh23Jera/Cdh23Jera involves: C57BL/6 J:174130 View
autosomal recessive nonsyndromic deafness 12 Cdh23sals/Cdh23sals involves: C57BL/6J J:147149 View
autosomal recessive nonsyndromic deafness 12 Cdh2312J/Cdh2312J involves: C57BL/6J J:174758 View
autosomal recessive nonsyndromic deafness 16 Strctm1Ugds/Strctm1Ugds involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J J:141421 View
autosomal recessive nonsyndromic deafness 18A Ush1cdfcr-4J/Ush1cdfcr-4J 129P3/J-Ush1cdfcr-4J/J J:278662 View
autosomal recessive nonsyndromic deafness 18A Ush1cdfcr-2J/Ush1cdfcr-2J B6;129S4 J:85400 View
autosomal recessive nonsyndromic deafness 18A Ush1cdfcr/Ush1cdfcr involves: BALB/cByJ J:85400 View
autosomal recessive nonsyndromic deafness 18B Otogvbd/Otogvbd involves: C3HeB/FeJ * C57BL/6J J:234038 View
autosomal recessive nonsyndromic deafness 22 Otoatm1Gpr/Otoatm1Gpr involves: 129S/SvEv J:192263 View
autosomal recessive nonsyndromic deafness 23 Pcdh15roda/Pcdh15roda BALB/c-Pcdh15roda J:220658 View
autosomal recessive nonsyndromic deafness 28 Triobptm1Tbf/Triobptm1Tbf C57BL/6-Triobptm1Tbf J:167947 View
autosomal recessive nonsyndromic deafness 29 Cldn14tm1Tbf/Cldn14tm1Tbf involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:85071 View
autosomal recessive nonsyndromic deafness 30 Myo3atm1.1Mckg/Myo3atm1.1Mckg C57BL/6-Myo3atm1.1Mckg J:166812 View
autosomal recessive nonsyndromic deafness 31 Whrnwi/Whrnwi involves: C57BL/6J * STOCK a Tyrp1b Myo5ad Oca2p Ednrbs J:269, J:5037, J:5538, J:77939 View
autosomal recessive nonsyndromic deafness 32 Cdc14aem1Tbf/Cdc14aem1Tbf involves: C57BL/6J J:257652 View
autosomal recessive nonsyndromic deafness 32 Cdc14atm1a(EUCOMM)Hmgu/Cdc14atm1b(EUCOMM)Hmgu involves: C57BL/6N * FVB J:257652 View
autosomal recessive nonsyndromic deafness 32 Cdc14atm1b(EUCOMM)Hmgu/Cdc14atm1b(EUCOMM)Hmgu involves: C57BL/6N * FVB J:257652 View
autosomal recessive nonsyndromic deafness 32 Cdc14atm1d(EUCOMM)Hmgu/Cdc14atm1d(EUCOMM)Hmgu involves: C57BL/6N * FVB J:257652 View
autosomal recessive nonsyndromic deafness 37 Myo6sv/Myo6sv involves: B10.HA/(33NX)Sn * C57BL/6J J:29898 View
autosomal recessive nonsyndromic deafness 39 Hgftm1.1Tbf/Hgftm1.1Tbf B6.Cg-Hgftm1.1Tbf/Tbf J:289982 View
autosomal recessive nonsyndromic deafness 39 Hgftm1Tbf/Hgftm1Tbf B6.Cg-Hgftm1Tbf/Tbf J:289982 View
autosomal recessive nonsyndromic deafness 42 Ildr1Gt(D178D03)Wrst/Ildr1Gt(D178D03)Wrst involves: 129S2/SvPas * Swiss Webster J:217755 View
autosomal recessive nonsyndromic deafness 42 Ildr1tm1.1Lwa/Ildr1tm1.1Lwa involves: 129S6/SvEvTac * C57BL/6 J:221594 View
autosomal recessive nonsyndromic deafness 42 Ildr1tm1(KOMP)Wtsi/Ildr1tm1(KOMP)Wtsi involves: C57BL/6N J:217755, J:221592 View
autosomal recessive nonsyndromic deafness 48 Cib2tm1.1Aela/Cib2tm1.1Aela involves: BALB/c * C57BL/6 * C57BL/6N J:262464 View
autosomal recessive nonsyndromic deafness 49 Marveld2tm1Sats/Marveld2tm1Sats B6.Cg-Marveld2tm1Sats J:261357 View
autosomal recessive nonsyndromic deafness 49 Marveld2tm1.1Sria/Marveld2tm1.1Sria involves: 129X1/SvJ * C57BL/6J J:201580 View
autosomal recessive nonsyndromic deafness 59 Pjvktm1Ugds/Pjvktm1Ugds involves: 129S2/SvPas * BALB/c * C57BL/6 J:111260 View
autosomal recessive nonsyndromic deafness 63 Tomtm1Btlr/Tomtm1Btlr C57BL/6J-Tomtm1Btlr J:137493 View
autosomal recessive nonsyndromic deafness 68 S1pr2tm1Ajml/S1pr2tm1Ajml either: (involves: 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6) J:231927 View
autosomal recessive nonsyndromic deafness 68 S1pr2stdf/S1pr2stdf involves: C57BL/6Brd * C57BL/6N J:240361 View
autosomal recessive nonsyndromic deafness 74 Msrb3tm1Hyk/Msrb3tm1Hyk involves: 129 * C57BL/6 J:206322 View
autosomal recessive nonsyndromic deafness 79 Tprnem1Pghu/Tprnem1Pghu B6.Cg-Tprnem1Pghu J:240563 View
autosomal recessive nonsyndromic deafness 88 Elmod3em1Jili/Elmod3em1Jili involves: C57BL/6 J:293683 View
autosomal recessive nonsyndromic deafness 93 Cabp2tm1b(KOMP)Mbp/Cabp2tm1b(KOMP)Mbp involves: C57BL/6N * FVB/N J:255028 View
autosomal recessive osteopetrosis 1 Tcirg1oc/Tcirg1oc B6C3Fe a/a-Tcirg1oc/J J:61295 View
autosomal recessive osteopetrosis 1 Tcirg1tm1Ypl/Tcirg1tm1Ypl involves: 129S4/SvJae * C57BL/6J J:58795 View
autosomal recessive osteopetrosis 2 Tnfsf11tm1Ywc/Tnfsf11tm1Ywc involves: 129P2/OlaHsd J:233265 View
autosomal recessive osteopetrosis 2 Tnfsf11tles/Tnfsf11tles involves: 129S6/SvEvTac * C57BL/6J J:179743 View
autosomal recessive osteopetrosis 2 Tnfsf11gum/Tnfsf11gum STOCK Tnfsf11gum/GrsrJ J:223062 View
autosomal recessive osteopetrosis 3 Car2n/Car2n involves: C57BL/6J * DBA/2J J:19268 View
autosomal recessive osteopetrosis 4 Clcn7tm1Tjj/Clcn7tm1Tjj involves: 129P2/OlaHsd * C57BL/6 J:67273 View
autosomal recessive osteopetrosis 4 Clcn7tm2Tjj/Clcn7tm2Tjj involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:67273 View
autosomal recessive osteopetrosis 5 Ostm1gl/Ostm1gl GL/Le Edardl-J +/+ Ostm1gl/J J:5561 View
autosomal recessive osteopetrosis 6 Plekhm1tm1.2Hzhao/Plekhm1tm1.2Hzhao involves: 129S1/Sv * C57BL/6J J:236517 View
autosomal recessive osteopetrosis 6 Ctsktm1(cre)Ska/Ctsk+
Plekhm1tm1.1Hzhao/Plekhm1tm1.1Hzhao
involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj J:236517 View
autosomal recessive osteopetrosis 8 Snx10em1Ael/Snx10em1Ael involves: 129 * C57BL/6J * C57BL/6JOlaHsd J:289051 View
autosomal recessive osteopetrosis 8 Snx10em2Ael/Snx10em2Ael involves: 129 * C57BL/6J * C57BL/6JOlaHsd J:289051 View
autosomal recessive polycystic kidney disease Pkhd1tm1Sswi/Pkhd1tm1Sswi B6.Cg-Pkhd1tm1Sswi J:186064 View
autosomal recessive polycystic kidney disease Pkhd1tm2Cjwa/Pkhd1tm2Cjwa either: B6.129(Cg)-Pkhd1tm2Cjwa or C.129(Cg)-Pkhd1tm2Cjwa J:187735 View
autosomal recessive polycystic kidney disease Pkhd1tm1Cjwa/Pkhd1tm1Cjwa involves: 129S6/SvEvTac * FVB/N J:140302 View
autosomal recessive polycystic kidney disease Pkhd1tm1.1Ggg/Pkhd1tm1.1Ggg involves: 129S/SvEv * 129S4/SvJae * C57BL/6 J:125113 View
autosomal recessive polycystic kidney disease Pkhd1tm1Gwu/Pkhd1tm1Gwu involves: C57BL/6 J:167782 View
autosomal recessive polycystic kidney disease Pkhd1tm1Gwu/Pkhd1tm1Gwu Not Specified J:143394 View
autosomal recessive pseudohypoaldosteronism type 1 Scnn1gtm1Bhk/Scnn1gtm1Bhk involves: 129P2/OlaHsd * C57BL/6 * DBA/2 J:50528 View
autosomal recessive pseudohypoaldosteronism type 1 Scnn1btm1Wsh/Scnn1btm1Wsh involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:53058 View
autosomal recessive Robinow syndrome Ror2tm1Anec/Ror2tm1Anec B6.129S1-Ror2tm1Anec J:134490 View
autosomal recessive Robinow syndrome Ror2tm1Ymi/Ror2tm1Ymi involves: 129P2/OlaHsd * C57BL/6 J:88955 View
autosomal recessive spinocerebellar ataxia 13 Grm1crv4/Grm1crv4 BALB/cPas-Grm1crv4 J:112290 View
autosomal recessive spinocerebellar ataxia 16 Stub1tm1Cpat/Stub1tm1Cpat involves: 129S/SvEv * C57BL/6 J:245069 View
autosomal recessive spinocerebellar ataxia 18 Grid2ho-15J/Grid2ho-15J involves: C3HeB/Fe J:220519 View
autosomal recessive spinocerebellar ataxia 18 Grid2tm1(cre)Mwa/Grid2tm1(cre)Mwa involves: C57BL/6N J:220519 View
Axenfeld-Rieger syndrome type 1 Pitx2tm1Kki/Pitx2tm1Kki involves: 129P2/OlaHsd * C57BL J:55455 View
Axenfeld-Rieger syndrome type 1 Pitx2tm1Rsd/Pitx2tm1Rsd involves: 129S1/Sv * 129X1/SvJ J:57673 View
Axenfeld-Rieger syndrome type 1 Pitx2tm1Sac/Pitx2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:51160 View
Axenfeld-Rieger syndrome type 1 Pitx2tm2Sac/Pitx2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:51160 View
Axenfeld-Rieger syndrome type 1 Pitx2tm1Jfm/Pitx2tm1Jfm involves: 129S4/SvJaeSor J:57674, J:87220 View
Axenfeld-Rieger syndrome type 1 Pitx2tm1Jfm/Pitx2tm2Jfm involves: 129S4/SvJaeSor J:87220 View
Axenfeld-Rieger syndrome type 1 Tg(Kera-PITX2*A)AHjal/0 involves: C57BL/6 * CBA J:93634 View
Axenfeld-Rieger syndrome type 1 Tg(Kera-PITX2*A)BHjal/0 involves: C57BL/6 * CBA J:93634 View
Bannayan-Riley-Ruvalcaba syndrome Ptentm1Mak/Pten+ involves: 129P2/OlaHsd * C57BL/6J J:63478 View
Bannayan-Riley-Ruvalcaba syndrome Ptentm1Ppp/Pten+ involves: 129S1/Sv * C57BL/6J J:49532 View
Bannayan-Riley-Ruvalcaba syndrome Ptentm1Rps/Pten+ involves: 129S1/Sv * C57BL/6J J:53065 View
Bardet-Biedl syndrome 1 Bbs1tm1Vcs/Bbs1tm1Vcs involves: 129S1/Sv * 129X1/SvJ J:128532 View
Bardet-Biedl syndrome 1 Bbs1tm2Vcs/Bbs1tm2Vcs
Tg(Pdgfra-cre)1Clc/0
involves: 129S6/SvEvTac * C57BL/6 J:194096 View
Bardet-Biedl syndrome 1 Bbs1Gt1Nk/Bbs1Gt1Nk involves: 129S7/SvEvBrd * C57BL/6J J:92950 View
Bardet-Biedl syndrome 2 Bbs2tm1Vcs/Bbs2tm1Vcs either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J) J:94467 View
Bardet-Biedl syndrome 2 Bbs2tm1.1Huss/Bbs2tm1.1Huss involves: 129S6/SvEv * C57BL/6 J:296033 View
Bardet-Biedl syndrome 4 Bbs4Gt1Nk/Bbs4Gt1Nk B6.129S7-Bbs4Gt1Nk J:279506 View
Bardet-Biedl syndrome 4 Bbs4tm1Vcs/Bbs4tm1Vcs involves: 129S1/Sv * 129X1/SvJ J:94467 View
Bardet-Biedl syndrome 4 Bbs4tm1Vcs/Bbs4tm1Vcs involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:90812 View
Bardet-Biedl syndrome 4 Bbs4Gt1Nk/Bbs4Gt1Nk involves: 129S7/SvEvBrd J:134093 View
Bardet-Biedl syndrome 4 Bbs4Gt1Nk/Bbs4Gt1Nk involves: 129S7/SvEvBrd * C57BL/6J J:92950 View
Bardet-Biedl syndrome 5 Bbs5tm1a(EUCOMM)Wtsi/Bbs5tm1a(EUCOMM)Wtsi C57BL/6-Bbs5tm1a(EUCOMM)Wtsi J:307098 View
Bardet-Biedl syndrome 6 Mkkstm1Vcs/Mkkstm1Vcs either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J) J:99276 View
Bardet-Biedl syndrome 8 Ttc8tm1Reed/Ttc8tm1Reed involves: 129 J:173465 View
Bardet-Biedl syndrome 10 Bbs10tm1.2Vmar/Bbs10tm1.2Vmar involves: 129P2/OlaHsd * C57BL/6 J:227230 View
Bardet-Biedl syndrome 16 Sdccag8em1Lji/Sdccag8em1Lji involves: C57BL/6 J:328191 View
Bardet-Biedl syndrome 16 Sdccag8em2Lji/Sdccag8em2Lji involves: C57BL/6 J:328191 View
Bardet-Biedl syndrome 17 Lztfl1tm1e(KOMP)Wtsi/Lztfl1tm1e(KOMP)Wtsi involves: 129S/SvEv * C57BL/6N J:226512 View
Bardet-Biedl syndrome 18 Bbip1tm1.1Gne/Bbip1tm1.1Gne involves: 129 * C57BL/6J * C57BL/6N J:204140 View
Beare-Stevenson cutis gyrata syndrome Fgfr2tm3Ewj/Fgfr2+ B6.129-Fgfr2tm3Ewj J:190491 View
Bernard-Soulier syndrome Gp1batm1Ware/Gp1batm1Ware involves: 129S1/Sv * 129X1/SvJ J:63389 View
Bernard-Soulier syndrome Gp1bbtm1Frla/Gp1bbtm1Frla involves: 129S2/SvPas * C57BL/6 J:135065 View
Bernard-Soulier syndrome Gp1bbtm2Frla/Gp1bbtm2Frla involves: 129S2/SvPas * C57BL/6 J:135065 View
Bernard-Soulier syndrome Gp1bbtm1Ware/Gp1bbtm1Ware Not Specified J:93756 View
Bernard-Soulier syndrome Gp1bbtm1Ware/Gp1bb+ Not Specified J:93756 View
beta thalassemia Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
B6;129P2-Hbb-b1tm1Unc Hbb-b2tm1Unc/J J:211331 View
beta thalassemia Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
involves: 129P2/OlaHsd J:154187 View
beta thalassemia Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 J:94421 View
beta thalassemia Ahsptm1Mjwe/Ahsptm1Mjwe
Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 J:94421 View
beta thalassemia Ahsptm1Mjwe/Ahsp+
Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 J:94421 View
beta thalassemia Ahsptm1.1Mjwe/Ahsptm1.1Mjwe
Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 J:94421 View
beta thalassemia Ahsptm1.1Mjwe/Ahsp+
Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 J:94421 View
beta thalassemia Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
Tg(HBB*)L2Pai/0
involves: 129P2/OlaHsd * C57BL/6 J:97548 View
beta thalassemia Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
involves: 129P2/OlaHsd * C57BL/6J J:30155 View
beta thalassemia Hbb-b1tm1Unc/Hbb-b1+
Hbb-b2tm1Unc/Hbb-b2+
involves: 129P2/OlaHsd * C57BL/6N J:185154 View
beta thalassemia Hbb-b1Rbc13/Hbb-b1Rbc13 involves: BALB/c * C57BL/6 J:190446 View
beta thalassemia Hbb-b1MommeD7/Hbb-b1MommeD7 involves: FVB/N J:190446 View
beta thalassemia Hbatm1(HBA)Tow/Hbatm1(HBA)Tow
Hbbtm2(HBG1,HBD,HBB*)Ryan/Hbbtm3(HBG1,HBB)Tow
Not Specified J:148521 View
beta thalassemia Hbatm1(HBA)Tow/Hbatm1(HBA)Tow
Hbbtm2(HBG1,HBD,HBB*)Ryan/Hbbtm2(HBG1,HBD,HBB*)Ryan
Not Specified J:148521 View
BH4-deficient hyperphenylalaninemia A Ptstm1Thny/Ptstm1Thny involves: 129/Sv * C57BL/6 J:84533 View
BH4-deficient hyperphenylalaninemia A Ptstm1Ich/Ptstm1Ich involves: 129X1/SvJ * C57BL/6J J:84764 View
BH4-deficient hyperphenylalaninemia B Gch1em1Ypt/Gch1em1Ypt C57BL/6-Gch1em1Ypt J:295169 View
biotinidase deficiency Btdtm1Bwol/Btdtm1Bwol B6.Cg-Btdtm1Bwol J:168391 View
Birt-Hogg-Dube syndrome Flcntm1Btt/Flcntm1Btt
Tg(Cdh16-cre)91Igr/0
involves: 129S4/SvJaeSor * C57BL/6 * ICR J:143922 View
Birt-Hogg-Dube syndrome Flcntm1Baba/Flcntm1.1Lss
Tg(Cdh16-cre)91Igr/0
involves: C57BL/6 * FVB/N * ICR * SJL J:130978 View
blepharophimosis, ptosis, and epicanthus inversus syndrome Foxl2tm1Gpil/Foxl2tm1Gpil either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6J) or (involves: 129S6/SvEvTac * NIHS-BC) J:90371 View
blepharophimosis, ptosis, and epicanthus inversus syndrome Foxl2tm1Tre/Foxl2tm1Tre involves: 129P2/OlaHsd * Black Swiss * CD-1 J:87737 View
Bloom syndrome ApcMin/Apc+
Blmtm1Grdn/Blm+
involves: 129P2/OlaHsd * 129S/SvEv * Black Swiss * C57BL/6J J:79058 View
Bloom syndrome Blmtm1Grdn/Blm+ involves: 129P2/OlaHsd * Black Swiss J:79058 View
Bloom syndrome Blmtm1Ches/Blmtm4Ches
Tg(Hsp70-1-cre)6Arge/0
involves: 129S6/SvEvTac * C57BL/6 * CBA J:112115 View
Bloom syndrome Blmtm1Ches/Blmtm4Ches
Tg(LGB-cre)74Acl/0
involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL J:112115 View
Bloom syndrome Blmtm1Ches/Blmtm1Ches involves: 129S6/SvEvTac * NIH Black Swiss J:50843 View
Bloom syndrome Blmtm3Brd/Blmtm3Brd involves: 129S7/SvEvBrd * C57BL/6 J:66261 View
Bloom syndrome Blmtm1Ches/Blmtm3Brd involves: 129S/SvEv * C57BL/6 * NIH Black Swiss J:86827 View
Bosch-Boonstra-Schaaf optic atrophy syndrome Nr2f1tm1Mjts/Nr2f1+ involves: 129S7/SvEvBrd J:286647 View
Bowen-Conradi syndrome Emg1tm1.1Btr/Emg1tm1.1Btr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 J:230556 View
brachydactyly type A1 Ihhtm1.1Dcha/Ihhtm1.1Dcha either: (involves: 129S/SvEv * FVB/N) or (involves: 129S/SvEv * FVB/N * ICR) J:147878 View
brachydactyly type A1C Gdf5Bp-5J/Gdf5+ C57BL/6J-Gdf5Bp-5J/GrsrJ J:200816 View
brachydactyly type A2 Gdf5Bp-5J/Gdf5+ C57BL/6J-Gdf5Bp-5J/GrsrJ J:200816 View
brachydactyly type C Gdf5Bp-5J/Gdf5+ C57BL/6J-Gdf5Bp-5J/GrsrJ J:200816 View
brachyolmia-amelogenesis imperfecta syndrome Ltbp3tm1Bdvc/Ltbp3tm1Bdvc involves: 129S6/SvEvTac J:220985 View
brain small vessel disease 1 Col4a1deltaex40/Col4a1+ B6.129S-Col4a1deltaex40 J:215446 View
branched-chain keto acid dehydrogenase kinase deficiency BckdkGt(VICT48)710Lex/BckdkGt(VICT48)710Lex B6.129S5/SvEvBrd-BckdkGt(VICT48)710Lex J:187971 View
branchiootorenal syndrome Eya1bor/Eya1bor C3HeB/FeJ-Eya1bor J:54408 View
branchiootorenal syndrome Six1Cwe/Six1Cwe C3HeB/FeJ-Six1Cwe J:149467 View
branchiootorenal syndrome Eya1tm1Rilm/Eya1+ either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) J:57313 View
branchiootorenal syndrome Eya1tm1Rilm/Eya1tm1Rilm either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) J:57313 View
branchiootorenal syndrome Eya1tm1Rilm/Eya1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:57313 View
brittle cornea syndrome 1 Zfp469em1Chms/Zfp469em1Chms C57BL/6J-Zfp469em1Chms J:311083 View
Brugada syndrome 1 Scn5atm1Care/Scn5a+ FVB.129P2-Scn5atm1Care/Care J:128657 View
Brugada syndrome 1 Scn5atm1Agrc/Scn5a+ involves: 129 J:166438 View
Brugada syndrome 7 Scn3btm1Clhh/Scn3btm1Clhh 129S/SvEv-Scn3btm1Clhh J:177262 View
bullous congenital ichthyosiform erythroderma Krt2Mhdadsk2/Krt2+ C3HeB/FeJ-Krt2Mhdadsk2/Ieg J:81301 View
bullous congenital ichthyosiform erythroderma Krt2Mhdadsk2/Krt2Mhdadsk2 involves: C3HeB/FeJ * C57BL/6J J:81301 View
CADASIL 1 Notch3hpbk/Notch3hpbk C57BL/6J-Notch3hpbk/GrsrJ J:222308 View
CADASIL 1 Gt(ROSA)26Sortm3(NOTCH3*R1031C)Sat/Gt(ROSA)26Sor+
Notch3Gt(PST033)Byg/Notch3Gt(PST033)Byg
Tg(Tagln-cre)1Her/0
involves: 129 * C57BL/6 * SJL J:171887 View
CADASIL 1 Gt(ROSA)26Sortm2(NOTCH3*C455R)Sat/Gt(ROSA)26Sor+
Notch3Gt(PST033)Byg/Notch3Gt(PST033)Byg
Tg(Tagln-cre)1Her/0
involves: 129 * C57BL/6 * SJL J:171887 View
CADASIL 1 Notch1tm1Grid/Notch1+
Notch3tm1Grid/Notch3tm1Grid
involves: 129S1/Sv * C57BL/6 J:227333 View
CADASIL 1 Gt(ROSA)26Sortm3(NOTCH3*R1031C)Sat/Gt(ROSA)26Sor+
Tg(Tagln-cre)1Her/0
involves: 129S2/SvEv * 129S6/SvEvTac * C57BL/6 * SJL J:171887 View
CADASIL 1 Notch3tm1.1Dwr/Notch3tm1.1Dwr involves: 129S/SvEv * Swiss J:191454 View
CADASIL 1 Notch3tm1.1Dwr/Notch3+ involves: 129S/SvEv * Swiss J:191454 View
CADASIL 1 Tg(Notch3*R169C)88Bbb/0 involves: FVB/N J:220006 View
campomelic dysplasia Sox9Bbfc/Sox9+ C57BL/6J-Sox9Bbfc/GrsrJ J:223062 View
campomelic dysplasia Sox9tm1.1Gsr/Sox9+ involves: 129P2/OlaHsd * C57BL/6 J:75124 View
campomelic dysplasia Sox9tm1Gsr/Sox9+
Tg(Pdx1-cre)6Cvw/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6J * CBA * FVB/N J:141017 View
campomelic dysplasia Sox9tm1Crm/Sox9+ involves: 129S7/SvEvBrd * C57BL/6 * CD-1 J:69875 View
campomelic dysplasia Sox9tm2Crm/Sox9tm2Crm
Tg(Col2a1-cre)1Bhr/0
involves: 129S7/SvEvBrd * C57BL/6 * SJL J:79879 View
campomelic dysplasia Sox9tm2Crm/Sox9+
Tg(Col2a1-cre)1Bhr/0
involves: 129S7/SvEvBrd * C57BL/6 * SJL J:79879 View
campomelic dysplasia Sox9tm2Crm/Sox9tm2Crm
Tg(Prrx1-cre)1Cjt/0
involves: 129S7/SvEvBrd * C57BL/6J * SJL/J J:79879 View
campomelic dysplasia Sox9tm2Crm/Sox9+
Tg(Prrx1-cre)1Cjt/0
involves: 129S7/SvEvBrd * C57BL/6J * SJL/J J:79879 View
Canavan disease Aspadeaf14/Aspadeaf14 BALB/c-Aspadeaf14 J:211825 View
Canavan disease Aspatm1Mata/Aspatm1Mata involves: 129S5/SvEvBrd J:89100, J:89099 View
Canavan disease Aspanur7/Aspanur7 involves: C57BL/6J J:143201, J:226682 View
Canavan disease Aspatm1a(EUCOMM)Wtsi/Aspatm1a(EUCOMM)Wtsi involves: C57BL/6J * C57BL/6N J:172582 View
carbamoyl phosphate synthetase I deficiency disease Cps1tm1Mw/Cps1tm1Mw involves: 129S7/SvEvBrd * C57BL/6 J:52334 View
Carney complex Prkar1atm1.2Lsk/Prkar1atm1.2Lsk
Tg(Tyr-cre)3Gfk/0
either: (involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) J:98799 View
Carney complex Prkar1atm1.1Lsk/Prkar1a+ involves: 129S1/Sv * 129X1/SvJ J:98799 View
Carney complex Prkar1atm1.1Lsk/Prkar1a+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:160299 View
Carney complex Prkar1atm1Gsm/Prkar1a+ involves: 129X1/SvJ J:93393 View
cataract 1 multiple types Gja8R205G/Gja8R205G B6.Cg-Gja8R205G J:195727 View
cataract 1 multiple types Gja8No2/Gja8No2 involves: 101 * C3H J:49492 View
cataract 1 multiple types Gja8No2/Gja8+ involves: 101 * C3H J:49492 View
cataract 1 multiple types Gja8tm1Paul/Gja8tm1Paul involves: 129S4/SvJae * C57BL/6J J:50894 View
cataract 2 multiple types CrygcChl3/CrygcChl3 involves: 102/El * C3H/El J:73804 View
cataract 2 multiple types CrygcChl3/Crygc+ involves: 102/El * C3H/El J:73804 View
cataract 2 multiple types Tg(CRYBB1-CRYGC*)#Jfhe/? involves: FVB/N J:181433 View
cataract 3 multiple types Crybb2Aey2/Crybb2+ C3HeB/FeJ-Crybb2Aey2 J:70508 View
cataract 3 multiple types Crybb2Lop19/Crybb2+ SJL/J-Crybb2Lop19/BocJ J:187061 View
cataract 3 multiple types Crybb2Phil/Crybb2Phil Swiss Webster J:11126 View
cataract 4 multiple types CrygdAey4/CrygdAey4 C3HeB/FeJ-CrygdAey4 J:78154 View
cataract 4 multiple types CrygdAey4/Crygd+ C3HeB/FeJ-CrygdAey4 J:78154 View
cataract 5 multiple types Tg(Hsf4/EGFP)N7Spbh/0 C57BL/6-Tg(Hsf4/EGFP)N7Spbh J:230205 View
cataract 5 multiple types Hsf4ldis1/Hsf4ldis1 involves: C57BL/6 * CAST/EiJ * RIIIS/J J:179658 View
cataract 6 multiple types Epha2Gt(KST085)Byg/Epha2Gt(KST085)Byg involves: 129P2/OlaHsd * C57BL/6 * FVB/N J:151310 View
cataract 9 multiple types CryaaAey7/CryaaAey7 C3HeB/FeJ-CryaaAey7/Ieg J:72928 View
cataract 9 multiple types CryaaAey7/Cryaa+ C3HeB/FeJ-CryaaAey7/Ieg J:72928 View
cataract 9 multiple types Cryaatm1Ady/Cryaatm1Ady involves: 129 J:157274 View
cataract 9 multiple types Cryaatm1Ady/Cryaa+ involves: 129 J:157274 View
cataract 9 multiple types Cryaatm1.1Ady/Cryaatm1.1Ady involves: 129 * C57BL/6 J:132296 View
cataract 9 multiple types Cryaatm1.1Ady/Cryaa+ involves: 129 * C57BL/6 J:132296 View
cataract 9 multiple types Cryaatm1Wawr/Cryaatm1Wawr involves: 129/Sv * 129S4/SvJae J:38210 View
cataract 9 multiple types Cryaatm1Wawr/Cryaatm1Wawr involves: 129S4/SvJae * C57BL/6 * DBA/2 J:38210 View
cataract 9 multiple types Cryaalop18/Cryaalop18 involves: CBA/CaGnLeJ J:34933 View
cataract 10 multiple types Cryba1Po1/Cryba1Po1 C3HeB/FeJ-Cryba1Po1 J:58912 View
cataract 10 multiple types Cryba1Po1/Cryba1+ C3HeB/FeJ-Cryba1Po1 J:58912 View
cataract 14 multiple types Gja3tm1.1Vmb/Gja3tm1.1Vmb involves: 129 * C57BL/6 J:227244 View
cataract 14 multiple types Gja3tm1.1Vmb/Gja3+ involves: 129 * C57BL/6 J:227244 View
cataract 15 multiple types MipCts/MipCts CTS/Shi J:196356 View
cataract 15 multiple types MipHfi/MipHfi involves: 101 * C3H J:14285 View
cataract 15 multiple types MipHfi/Mip+ involves: 101 * C3H J:14285 View
cataract 15 multiple types MipCat-Fr/MipCat-Fr involves: A/J J:31574 View
cataract 15 multiple types MipCts/Mip+ involves: C57BL/6J * CTS/Shi J:196356 View
cataract 15 multiple types MipCat-Tohm/MipCat-Tohm involves: DDI J:82971 View
cataract 15 multiple types MipCat-Lop/Mip+ involves: STOCK Rb(6.15)1Ald J:31574 View
cataract 16 multiple types Cryabtm1.1Ady/Cryabtm1.1Ady involves: 129X1/SvJ * C57BL/6 J:210399 View
cataract 19 multiple types Lim2To3/Lim2To3 involves: 102 * C3H/He * T STOCK J:46338 View
cataract 19 multiple types Lim2To3/Lim2+ involves: 102 * C3H/He * T STOCK J:46338 View
cataract 19 multiple types Tg(Lim2*G15V)1Rlc/0 involves: C57BL/6 * SJL J:100078 View
cataract 19 multiple types Tg(Lim2*G15V)1Rlc/Tg(Lim2*G15V)1Rlc involves: C57BL/6 * SJL J:100078 View
cataract 20 multiple types CrygsOpj/CrygsOpj involves: 102 * C3H/He * T STOCK J:34877, J:68109 View
cataract 20 multiple types CrygsOpj/Crygs+ involves: 102 * C3H/He * T STOCK J:34877, J:68109 View
cataract 20 multiple types Crygsrncat/Crygsrncat Kunming J:77271 View
cataract 21 multiple types MafOfl/Maf+ either: 102/ElH or C3H/HeH J:82475 View
cataract 30 Tg(Vim*R113C)1Tmm/0 B6.CBA-Tg(Vim*R113C)1Tmm J:145782 View
cataract 39 multiple types CrygbS11R/CrygbS11R A/J-CrygbS11R J:132502 View
cataract 39 multiple types CrygbS11R/Crygb+ A/J-CrygbS11R J:132502 View
cataract 39 multiple types CrygbClapper/CrygbClapper C57BL/6J-CrygbClapper J:100851 View
cataract 39 multiple types CrygbClapper/Crygb+ C57BL/6J-CrygbClapper J:100851 View
cataract 39 multiple types CrygbNop/CrygbNop Not Specified J:7589 View
cataract 39 multiple types CrygbNop/Crygb+ Not Specified J:7589 View
Cayman type cerebellar ataxia Atcayji-hes/Atcayji-hes C3H/HeJ-Atcayji-hes J:85793 View
Cayman type cerebellar ataxia Atcayji/Atcayji JIGR J:85793 View
Cayman type cerebellar ataxia Atcayswd/Atcayswd Not Specified J:85793 View
CEDNIK syndrome Snap29tm1c(EUCOMM)Wtsi/Snap29tm1c(EUCOMM)Wtsi
Tg(KRT14-cre)1Cgn/0
involves: C57BL/6 * C57BL/6N * DBA/2 J:236759 View
CEDNIK syndrome Snap29tm1b(EUCOMM)Wtsi/Snap29tm1b(EUCOMM)Wtsi involves: C57BL/6N * FVB/N J:236759 View
central core disease Ryr1m1Nisw/Ryr1+ 129S1.B6-Ryr1m1Nisw J:219285 View
central core disease Ryr1tm1.1Dhm/Ryr1+ involves: 129S2/SvPasCrl * 129S6/SvEvTac J:155825 View
central core disease Ryr1tm1Tno/Ryr1tm1Tno involves: 129S4/SvJae * C57BL/6J J:18895 View
central precocious puberty 2 Mkrn3em1Rhu/Mkrn3+ involves: C57BL/6 J:305000 View
cerebellar ataxia type 42 Cacna1gem1Ftan/Cacna1gem1Ftan C57BL/6NCrSlc-Cacna1gem1Ftan J:278129 View
cerebellar ataxia type 42 Cacna1gem1Ftan/Cacna1g+ C57BL/6NCrSlc-Cacna1gem1Ftan J:278129 View
cerebellar ataxia, mental retardation and dysequlibrium syndrome Atp8a2wl-vmd/Atp8a2wl-vmd C3H/HeSnJ-Atp8a2wl-vmd/J J:222308 View
cerebellar ataxia, mental retardation and dysequlibrium syndrome Car8wdl/Car8wdl C57BLKS/J-Car8wdl/GrsrJ J:230904 View
cerebellar ataxia, mental retardation and dysequlibrium syndrome Atp8a2wl-3J/Atp8a2wl-3J CBA/J-Atp8a2wl-3J/J J:222308 View
cerebellar ataxia, mental retardation and dysequlibrium syndrome Atp8a2wl/Atp8a2wl involves: C57BL/6J J:222308 View
cerebellar ataxia, mental retardation and dysequlibrium syndrome Atp8a2wl/Atp8a2wl Not Specified J:222308 View
Charcot-Marie-Tooth disease axonal type 2K Gdap1tm1.2Geno/Gdap1tm1.2Geno involves: 129 * C57BL/6 J:224701 View
Charcot-Marie-Tooth disease axonal type 2O Dync1h1tm1.1Sjki/Dync1h1+ involves: 129 * 129S1/SvImJ * C57BL/6 * C57BL/6J J:264493 View
Charcot-Marie-Tooth disease axonal type 2P Lrsam1Gt(RRK461)Byg/Lrsam1Gt(RRK461)Byg involves: 129P2/OlaHsd J:196447 View
Charcot-Marie-Tooth disease axonal type 2Q Dhtkd1tm1Mmgu/Dhtkd1tm1Mmgu involves: 129S6/SvEvTac * C57BL/6J J:288186 View
Charcot-Marie-Tooth disease axonal type 2Q Dhtkd1tm1Zgwg/Dhtkd1tm1Zgwg involves: C57BL/6 J:267178 View
Charcot-Marie-Tooth disease dominant intermediate C Yarstm1.1Rwb/Yarstm1.1Rwb involves: C57BL/6N * FVB/N J:310162 View
Charcot-Marie-Tooth disease recessive intermediate D Cox6a1tm1(KOMP)Wtsi/Cox6a1tm1(KOMP)Wtsi involves: C57BL/6JJcl * C57BL/6N J:230212 View
Charcot-Marie-Tooth disease type 1A Pmp22Tr-J/Pmp22+ B6.Cg-Pmp22Tr-J Krt25Re/+ +/J J:3394, J:101812 View
Charcot-Marie-Tooth disease type 1A Tg(PMP22)C3Fbas/? B6.Cg-Tg(PMP22)C3Fbas J:237901 View
Charcot-Marie-Tooth disease type 1A Tg(PMP22)C61Clh/0 B6.Cg-Tg(PMP22)C61Clh J:158350 View
Charcot-Marie-Tooth disease type 1A Pmp22Tr-2J/Pmp22+ C57BL/6J-Pmp22Tr-2J/GrsrJ J:201866 View
Charcot-Marie-Tooth disease type 1A Tg(Pmp22)247Ueli/0 involves: C3H * C57BL/6 J:98118 View
Charcot-Marie-Tooth disease type 1A Pmp22Tr-J/Pmp22+ involves: C57BL/6 J:3394, J:98231 View
Charcot-Marie-Tooth disease type 1A Tg(Pmp22)My41Clh/0 involves: C57BL/6J * CBA/Ca J:76795 View
Charcot-Marie-Tooth disease type 1A Tg(PMP22)C22Clh/0 involves: C57BL/6J * CBA/Ca J:78221, J:76795 View
Charcot-Marie-Tooth disease type 1A Tg(PMP22-tTA)JY13Clh/0
Tg(tetO/CMV-Pmp22)JP18Clh/0
involves: C57BL/6J * CBA/Ca J:69545 View
Charcot-Marie-Tooth disease type 1B Mpztm3.1Wra/Mpztm3.1Wra FVB.129S2(Cg)-Mpztm1.1Wra J:241742 View
Charcot-Marie-Tooth disease type 1B Mpztm3.1Wra/Mpz+ FVB.129S2(Cg)-Mpztm3.1Wra J:241742 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz)88.1Mfel/0 FVB/N-Tg(Mpz)88.1Mfel J:77658 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz)88.2Mfel/0 FVB/N-Tg(Mpz)88.2Mfel J:77658 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz)88.4Mfel/0 FVB/N-Tg(Mpz)88.4Mfel J:77658 View
Charcot-Marie-Tooth disease type 1B Mpztm1Msch/Mpztm1Msch involves: 129S7/SvEvBrd J:42838 View
Charcot-Marie-Tooth disease type 1B Mpztm1Msch/Mpz+ involves: 129S7/SvEvBrd J:42838 View
Charcot-Marie-Tooth disease type 1B Mpztm1Msch/Mpz+
Tg(Mpz*S63X)31Mes/0
involves: 129S7/SvEvBrd * FVB/N J:105751 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz*S63X)30Mes/0 involves: FVB/N J:105751 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz*S63X)31Mes/0 involves: FVB/N J:105751 View
Charcot-Marie-Tooth disease type 1C Litaftm1.1Cwc/Litaftm1.1Cwc B6.Cg-Litaftm1.1Cwc J:314784 View
Charcot-Marie-Tooth disease type 1C Tg(CMV-LITAF*W116G)#Lli/Tg(CMV-LITAF*W116G)#Lli FVB-Tg(CMV-LITAF*W116G)#Lli J:194981 View
Charcot-Marie-Tooth disease type 1E Pmp22Tr-2J/Pmp22+ C57BL/6J-Pmp22Tr-2J/GrsrJ J:201866 View
Charcot-Marie-Tooth disease type 2A1 Kif1btm1Noh/Kif1b+ involves: 129S4/SvJae * C57BL/6J J:69772 View
Charcot-Marie-Tooth disease type 2A2A Tg(Eno2-MFN2*R94Q)L51Ugfm/0 involves: C57BL/6 * C57BL/6J * DBA/2 J:158936 View
Charcot-Marie-Tooth disease type 2A2A Tg(Eno2-MFN2*R94Q)L51Ugfm/0 involves: C57BL/6 * DBA/2 J:173431 View
Charcot-Marie-Tooth disease type 2A2A Tg(Eno2-MFN2*R94Q)L87Ugfm/Tg(Eno2-MFN2*R94Q)L87Ugfm involves: C57BL/6 * DBA/2 J:173431 View
Charcot-Marie-Tooth disease type 2A2A Gt(ROSA)26Sortm1(CAG-MFN2*T105M)Dple/Gt(ROSA)26Sor+
Tg(Nes-cre)1Kln/0
involves: C57BL/6 * SJL J:251584 View
Charcot-Marie-Tooth disease type 2A2A Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc/Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc Not Specified J:132035 View
Charcot-Marie-Tooth disease type 2B1 Lmnatm1Stw/Lmnatm1Stw involves: 129S1/Sv J:75378 View
Charcot-Marie-Tooth disease type 2D GarsNmf249/Gars+ C57BL/6J-GarsNmf249/J J:112221 View
Charcot-Marie-Tooth disease type 2D GarsC201R/Gars+ involves: BALB/cAnN * C3H/HeH * C57BL/6J J:149830, J:179811 View
Charcot-Marie-Tooth disease type 2D GarsNmf249/Gars+ involves: C57BL/6J * CAST/Ei J:179811 View
Charcot-Marie-Tooth disease type 2D Garsem1Rwb/Garsem2Rwb involves: C57BL/6NJ * FVB/NJ J:284948 View
Charcot-Marie-Tooth disease type 2E Nefltm2.1Liem/Nefl+ B6.Cg-Nefltm2.1Liem J:220605 View
Charcot-Marie-Tooth disease type 2E Tg(tetO-NEFL)173.2Jpj/0
Tg(THY1-tTA)177Jpj/0
involves: C3H * C57BL/6 J:160704 View
Charcot-Marie-Tooth disease type 2E Tg(NEFL*E397K)#Milg/0 Not Specified J:173771 View
Charcot-Marie-Tooth disease type 3 Pmp22Tr-2J/Pmp22+ C57BL/6J-Pmp22Tr-2J/GrsrJ J:201866 View
Charcot-Marie-Tooth disease type 3 Mpztm1Msch/Mpztm1Msch involves: 129S7/SvEvBrd J:42838 View
Charcot-Marie-Tooth disease type 3 Tg(Mpz*S63C)32Mes/0 involves: FVB/N J:105751 View
Charcot-Marie-Tooth disease type 3 Tg(Mpz*S63C)33Mes/0 involves: FVB/N J:105751 View
Charcot-Marie-Tooth disease type 4B1 Mtmr2tm1.1Abol/Mtmr2tm1.1Abol involves: 129S2/SvPas J:94373 View
Charcot-Marie-Tooth disease type 4B1 Mtmr2tm1Ueli/Mtmr2tm1Ueli involves: 129S6/SvEvTac * C57BL/6 J:104120 View
Charcot-Marie-Tooth disease type 4B2 Sbf2Gt(XH212)Byg/Sbf2Gt(XH212)Byg involves: 129P2/OlaHsd * C57BL/6 J:133042 View
Charcot-Marie-Tooth disease type 4B2 Sbf2Gt(RRF511)Byg/Sbf2Gt(RRF511)Byg involves: 129P2/OlaHsd * C57BL/6 J:133391 View
Charcot-Marie-Tooth disease type 4B3 Sbf1em1Frobi/Sbf1em1Frobi C57BL/6N-Sbf1em1Frobi J:326685 View
Charcot-Marie-Tooth disease type 4C Sh3tc2tm1.1Rchr/Sh3tc2tm1.1Rchr involves: 129/Sv * FVB/N J:153705 View
Charcot-Marie-Tooth disease type 4D Ndrg1tm1Myta/Ndrg1tm1Myta involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:89888 View
Charcot-Marie-Tooth disease type 4E Egr2tm2Jmi/Egr2tm2Jmi B6.Cg-Egr2tm2Jmi J:145949 View
Charcot-Marie-Tooth disease type 4E Egr2tm1Jmi/Egr2tm1Jmi Not Specified J:96641 View
Charcot-Marie-Tooth disease type 4H Fgd4tm1.1Ics/Fgd4tm1.1Ics Not Specified J:190437 View
Charcot-Marie-Tooth disease type 4J Fig4plt1/Fig4plt1
Tg(ACTB-Fig4*I41T)705Mm/0
involves: 129 * C3H * C57BL/6J * CAST/Ei * SJL J:173446 View
Charcot-Marie-Tooth disease type 4J Fig4plt1/Fig4plt1 involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL J:122737 View
Charlevoix-Saguenay spastic ataxia Sacstm2Bebr/Sacstm2Bebr involves: C57BL/6 J:217753 View
Charlevoix-Saguenay spastic ataxia Sacstm1(NCOM)Mfgc/Sacstm1(NCOM)Mfgc Not Specified J:182034 View
Chediak-Higashi syndrome Lystbg/Lystbg B6.C3Rl-Lystbg J:5078, J:5338, J:5405, J:5471, J:5514, J:5590, J:6302, J:4978 View
Chediak-Higashi syndrome Lystbg/Lystbg B6.C3Rl-Lystbg/J J:6801 View
Chediak-Higashi syndrome Lystbg-18J/Lystbg-18J B6.Cg-Lystbg-18J/Boc J:222308 View
Chediak-Higashi syndrome Lystbg-14J/Lystbg-14J C3Fe;B6-Lystbg-14J J:85200 View
Chediak-Higashi syndrome Lystbg-grey/Lystbg-grey C57BL/6-Lystbg-grey J:106442 View
Chediak-Higashi syndrome Lystbg-2Btlr/Lystbg-2Btlr C57BL/6J-Lystbg-2Btlr J:133617 View
Chediak-Higashi syndrome Lystbg-Btlr/Lystbg-Btlr C57BL/6J-Lystbg-Btlr J:133616 View
Chediak-Higashi syndrome Lystbg-Lac/Lystbg-Lac CBA/CaLac-Lystbg-Lac J:29745 View
Chediak-Higashi syndrome Lystbg-slt/Lystbg-slt YZ57/Ch J:25388 View
cherubism Sh3bp2tm1.1Ics/Sh3bp2tm1.1Ics involves: 129S2/SvPas * C57BL/6 J:221901 View
cherubism Sh3bp2tm1Bjro/Sh3bp2tm1Bjro involves: 129S4/SvJae * BALB/cJ * C57BL/6J J:117880 View
childhood hypophosphatasia Alpltm1Sor/Alpltm1Sor either: (involves: 129S7/SvEvBrd-Alpltm1Sor) or (involves: 129S7/SvEvBrd * C57BL/6) J:28394 View
chondrodysplasia with joint dislocations gPAPP type Bpnt2tm1.2Aros/Bpnt2tm1.2Aros B6(SJL)-Bpnt2tm1.2Aros J:273179 View
choreaacanthocytosis Vps13atm1Asan/Vps13atm1Asan involves: 129S/SvEv * C57BL/6J J:96243 View
CINCA Syndrome Nlrp3tm3.1Hhf/Nlrp3+ involves: 129 J:202147 View
cleidocranial dysplasia Runx2tm1Kish/Runx2tm1Kish involves: 129P2/OlaHsd * C57BL/6 J:40783, J:53069, J:54095 View
cleidocranial dysplasia Runx2tm1Kish/Runx2+ involves: 129P2/OlaHsd * C57BL/6 J:40783 View
cleidocranial dysplasia Runx2tm1Mjo/Runx2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:40784, J:53868 View
cleidocranial dysplasia Runx2tm1Jals/Runx2tm1Jals involves: 129S7/SvEvBrd * C57BL/6 J:143532 View
Clouston syndrome Gjb6tm2.2Kwi/Gjb6tm2.2Kwi involves: 129P2/OlaHsd * BALB/c * C57BL/6 * CD-1 * SJL J:208123 View
Cockayne syndrome Ercc6tm1Gvh/Ercc6tm1Gvh
Xpatm1Hvs/Xpatm1Hvs
B6.129P2-Xpatm1Hvs Ercc6tm1Gvh J:122013 View
Cockayne syndrome Ercc6tm1Gvh/Ercc6tm1Gvh B6J.129P2-Ercc6tm1Gvh J:219993 View
Cockayne syndrome Ercc8tm1Jhjh/Ercc8tm1Jhjh B6J.129P2-Ercc8tm1Jhjh J:219993 View
Cockayne syndrome Ercc6tm1Gvh/Ercc6tm1Gvh
Xpatm1Hvs/Xpatm1Hvs
involves: 129P2/OlaHsd * C57BL/6J J:122013 View
Cockayne syndrome Ercc8tm1Jhjh/Ercc8tm1Jhjh involves: 129P2/OlaHsd * C57BL/6J J:74959 View
Cockayne syndrome Ercc6tm1Gvh/Ercc6tm1Gvh involves: 129P2/OlaHsd * FVB J:40211 View
Coffin-Siris syndrome 1 Arid1bem1Hzhu/Arid1b+ C57BL/6J-Arid1bem1Hzhu J:256668 View
Cohen syndrome Vps13btm1.2Ics/Vps13btm1.2Ics involves: C57BL/6N J:296007 View
common variable immunodeficiency Nfkb2Lym1/Nfkb2+ BALB/c-Nfkb2Lym1 J:206674 View
common variable immunodeficiency Icostm1Flv/Icostm1Flv involves: 129/Sv * C57BL/6 J:87123 View
common variable immunodeficiency Nfkb2tm2Brv/Nfkb2tm2Brv involves: 129S1/Sv * C57BL/6 J:206674 View
common variable immunodeficiency Nfkb2Lym1/Nfkb2Lym1 involves: BALB/c J:206674 View
common variable immunodeficiency Icostm1Shr/Icostm1Shr Not Specified J:87124 View
complex cortical dysplasia with other brain malformations 7 Tubb2bbrdp/Tubb2bbrdp involves: A/J * FVB J:201099 View
Compton-North congenital myopathy Cntn1usl/Cntn1usl B6.MRL-Cntn1usl/GrsrJ J:222308 View
Compton-North congenital myopathy Cntn1m1J/Cntn1m1J B6;C-Cntn1m1J/GrsrJ J:222308 View
Compton-North congenital myopathy Cntn1usl/Cntn1usl MRL/MpJ-Faslpr Cntn1usl/GrsrJ J:222308 View
congenital afibrinogenemia Fggtm1Fjc/Fggtm1Fjc involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:75302 View
congenital amegakaryocytic thrombocytopenia Mpltm1Fjs/Mpltm1Fjs involves: 129 * C57BL/6J J:87416 View
congenital anomalies of kidney and urinary tract syndrome with or without hearing loss, abnormal ears, or developmental delay Pbx1em1Dunw/Pbx1em1Dunw C57BL/6J-Pbx1em1Dunw J:320934 View
congenital central hypoventilation syndrome Phox2btm2Jbr/Phox2b+ involves: 129S2/SvPas * C57BL/6 J:131365 View
congenital diarrhea 5 with tufting enteropathy EpcamGt(RST412)Byg/EpcamGt(RST412)Byg involves: 129P2/OlaHsd * C57BL/6 J:195002 View
congenital disorder of glycosylation type IIa Mgat2tm1.1Jxm/Mgat2tm1.1Jxm involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:80661 View
congenital disorder of glycosylation type IIa Mgat2tm1.1Jxm/Mgat2tm1.1Jxm involves: 129S1/Sv * 129X1/SvJ * ICR J:80661 View
congenital disorder of glycosylation type IIc Slc35c1tm1Cknr/Slc35c1tm1Cknr involves: 129/Sv * 129P2/OlaHsd * C57BL/6 J:121151 View
congenital generalized lipodystrophy type 1 Agpat2tm1Garg/Agpat2tm1Garg involves: 129S6/SvEvTac J:146649 View
congenital generalized lipodystrophy type 2 Bscl2tm1Geno/Bscl2tm1Geno B6.129P2-Bscl2tm1Geno J:200947 View
congenital generalized lipodystrophy type 2 Bscl2tm1.2Gliu/Bscl2tm1.2Gliu involves: 129 * 129S4/SvJaeSor * C57BL/6 * FVB/N J:173404, J:211072 View
congenital generalized lipodystrophy type 2 Bscl2tm1.1Lchan/Bscl2tm1.1Lchan involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:211142 View
congenital generalized lipodystrophy type 4 Cavin1tm1Pfp/Cavin1tm1Pfp involves: 129S6/SvEvTac * C57BL/6 J:150419 View
congenital heart defects, dysmorphic facial features, and intellectual developmental disorder Cdk13tm1a(EUCOMM)Hmgu/Cdk13tm1a(EUCOMM)Hmgu involves: C57BL/6N J:291583 View
congenital hereditary endothelial dystrophy of cornea Slc4a11tm1.1Jrcy/Slc4a11tm1.1Jrcy involves: C57BL/6 J:214272 View
congenital megabladder Myocdem1Blk/Myocdtm1.1Msp involves: 129 J:283803 View
congenital megabladder Myocdtm1.1Msp/mgb involves: 129/Sv * FVB/N J:283803 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-2J/Lama2dy-2J B6.WK-Lama2dy-2J J:97464 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-7J/Lama2dy-7J C57BL/6J-Lama2dy-7J/J J:134367 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-8J/Lama2dy-8J C57BL/6J-Lama2dy-8J/GrsrJ J:149729 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Stk/Lama2tm1Stk involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR J:43145, J:167230 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy/Lama2dy involves: 129P1/Re J:13125 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv J:170192 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv * Black Swiss J:59089 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv * Black Swiss * FVB/N J:49435 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-6J/Lama2dy-6J involves: C57BL/6JEi * DBA/2J J:56803 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-Pas/Lama2dy-Pas involves: non-inbred stock J:102806 View
congenital muscular dystrophy due to integrin alpha-7 deficiency Itga7tm1Umr/Itga7tm1Umr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:82116 View
congenital muscular dystrophy due to LMNA mutation Lmnatm2.1Gbon/Lmnatm2.1Gbon involves: 129 * C57BL/6 J:180603 View
congenital myasthenic syndrome 3A Tg(Ckm-Chrnd*S262T)40Cgz/0 involves: C57BL/6 * DBA/2 J:31221 View
congenital myasthenic syndrome 4A Chrnetm2Vwi/Chrnetm2Vwi involves: 129P2/OlaHsd * C57BL/6 J:182046 View
congenital myasthenic syndrome 4A Tg(Ckm-Chrne*L269F)5Cgz/? involves: FVB/NJ J:193524 View
congenital myasthenic syndrome 4C Chrnetm1Vwi/Chrnetm1Vwi involves: 129P2/OlaHsd * C57BL/6 J:128178 View
congenital myasthenic syndrome 5 Colqtm1Jrs/Colqtm1Jrs involves: 129S1/Sv * 129X1/SvJ J:54006 View
congenital myasthenic syndrome 6 Chattm1Fhg/Chattm1Fhg involves: 129S2/SvPas * C57BL/6 J:81738 View
congenital myasthenic syndrome 6 Chattm1.1Jrs/Chattm1.1Jrs Not Specified J:91066 View
congenital myasthenic syndrome 8 Agrnnmf380/Agrnnmf380 C57BL/6J-Agrnnmf380/J J:176117 View
congenital myasthenic syndrome 9 Musktm1Vwi/Musktm1Vwi
Tg(Ckmm-cre)5Khn/0
involves: C57BL/6J * FVB J:106867 View
congenital myasthenic syndrome 9 Musktm1Vwi/Musktm1.1Vwi
Tg(Ckmm-cre)5Khn/0
involves: C57BL/6J * FVB J:106867 View
congenital myasthenic syndrome 9 Musktm1.1Vwi/Musktm2Vwi Not Specified J:141024 View
congenital myasthenic syndrome 10 Dok7tm2Yyam/Dok7tm2Yyam involves: 129P2/OlaHsd * C57BL/6J J:213767 View
congenital myasthenic syndrome 11 Rapsnem1Gan/Rapsnem1Gan C57BL/6J-Rapsnem1Gan J:282816 View
congenital myasthenic syndrome 12 Gfpt1tm1c(EUCOMM)Wtsi/Gfpt1tm1c(EUCOMM)Wtsi
Tg(Ckmm-cre)5Khn/0
involves: C57BL/6J * C57BL/6N * SJL/J J:265013 View
congenital myasthenic syndrome 19 Col13a1tm3.1Pih/Col13a1tm3.1Pih involves: 129S1/Sv * 129X1/SvJ J:242846 View
congenital nystagmus 1 Frmd7tm1b(KOMP)Wtsi/Frmd7tm1b(KOMP)Wtsi involves: C57BL/6 * C57BL/6N J:299010 View
congenital nystagmus 1 Frmd7tm1b(KOMP)Wtsi/Y involves: C57BL/6 * C57BL/6N J:299010 View
congenital secretory chloride diarrhea 1 Slc26a3tm1Sole/Slc26a3tm1Sole involves: 129S6/SvEvTac * C57BL/6 J:117587 View
congenital stationary night blindness 1B Grm6nob7/Grm6nob7 C57BL/6J-Grm6nob7 J:229885 View
congenital stationary night blindness 1B Grm6nob8/Grm6nob8 CBA/CaJ J:240996 View
congenital stationary night blindness 1D Slc24a1tm1Xen/Slc24a1tm1Xen involves: C57BL/6 J:226323 View
congenital stationary night blindness 1E Gpr179nob5/Gpr179nob5 involves: C3H J:185567 View
congenital stationary night blindness 1F Lrit3tm1Lex/Lrit3tm1Lex involves: 129S5/SvEvBrd * C57BL/6 J:214644 View
congenital stationary night blindness autosomal dominant 1 Tg(Rho*G90D*A337V)202Sie/0 involves: C57BL/6 * DBA J:188632 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-2J/Pde6brd1-2J C57BL/6J-Pde6brd1-2J/J J:82238 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd1/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd1/Pde6batrd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd2/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd2/Pde6batrd2 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd3/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6batrd3/Pde6batrd3 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-1H/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-2H/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-3H/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-3H/Pde6brd1-3H involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-4H/Pde6brd1 involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1-4H/Pde6brd1-4H involves: BALB/cAnN * C3H/HeN J:75964 View
congenital stationary night blindness autosomal dominant 2 Pde6brd1/Pde6brd1 Not Specified J:24999 View
cortical dysplasia-focal epilepsy syndrome Cntnap2tm1Pele/Cntnap2tm1Pele B6.129-Cntnap2tm1Pele J:177110 View
cortisone reductase deficiency 2 Hsd11b1tm1Yko/Hsd11b1tm1Yko involves: 129P2/OlaHsd * MF1 J:37960, J:45085, J:72402 View
Costello syndrome Hrastm2Xbr/Hrastm2Xbr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N J:137729 View
Costello syndrome Hrastm1Jaf/Hras+
Tg(CAG-cre)13Miya/0
involves: 129S6/SvEvTac * Black Swiss * C57BL/6 J:204891 View
craniotubular dysplasia Ikegawa type Tmem53em1Ikeg/Tmem53em1Ikeg Not Specified J:306057 View
cystathioninuria Cthtm1Iish/Cthtm1Iish B6.129-Cthtm1Iish J:166184 View
cystic fibrosis Cftrtm1Eur/Cftrtm1Eur B6.129P2-Cftrtm1Eur J:189205 View
cystic fibrosis Cftrtm1Unc/Cftrtm1Unc B6.129P2-Cftrtm1Unc/J J:58571, J:112450 View
cystic fibrosis Cftrtm2Mrc/Cftrtm2Mrc B6.129S6-Cftrtm2Mrc J:112450 View
cystic fibrosis Cftrtm3Mrc/Cftrtm3Mrc B6.129S6-Cftrtm3Mrc J:112450 View
cystic fibrosis Cftrtm1Kth/Cftrtm1Kth B6.129S7-Cftrtm1Kth J:112450 View
cystic fibrosis Cftrem3Cwr/Cftrem3Cwr C57BL/6J-Cftrem3Cwr/Cwr J:262928 View
cystic fibrosis Cftrtm1Unc/Cftrtm1Unc involves: 129P2/OlaHsd J:2079 View
cystic fibrosis Cftrtm1Hgu/Cftrtm1Hgu involves: 129P2/OlaHsd J:24119 View
cystic fibrosis Cftrtm3Hgu/Cftrtm3Hgu involves: 129P2/OlaHsd J:32766 View
cystic fibrosis Cftrtm2Hgu/Cftrtm2Hgu involves: 129P2/OlaHsd * C57BL/6 J:74740 View
cystic fibrosis Cftrtm1Eur/Cftrtm1Eur involves: 129P2/OlaHsd * FVB/N J:28979 View
cystic fibrosis Cftrtm1Hgu/Cftrtm1Hgu involves: 129P2/OlaHsd * MF1 J:14614 View
cystic fibrosis Cftrtm1Hsc/Cftrtm1Hsc involves: 129S1/Sv * 129X1/SvJ * CD-1 J:31759 View
cystic fibrosis Cftrtm3Bay/Cftrtm3Bay involves: 129S7/SvEvBrd J:29656 View
cystic fibrosis Cftrtm1Kth/Cftrtm1Kth involves: 129S7/SvEvBrd * C57BL/6J J:29074 View
cystic fibrosis Cftrtm1Bay/Cftrtm1Bay involves: 129S7/SvEvBrd * C57BL/6J J:15244 View
cystic fibrosis Cftrtm1Cam/Cftrtm1Cam involves: 129S/SvEv J:2584 View
cystic fibrosis Cftrtm2Cam/Cftrtm2Cam involves: 129S/SvEv J:27734 View
cystic fibrosis Cftrtm1.1Sdw/Cftrtm1.1Sdw involves: C57BL/6 * C57BL/6J J:323560 View
cystinosis Ctnstm1Antc/Ctnstm1Antc involves: 129/Sv * C57BL/6 J:79610 View
dentinogenesis imperfecta Dspptm1Kul/Dspptm1Kul involves: 129/Sv * C57BL/6 J:84378 View
Denys-Drash syndrome Wt1tm1Mlh/Wt1+ 129P2/OlaHsd-Wt1tm1Mlh J:135449 View
Denys-Drash syndrome Wt1tm2Hst/Wt1+ chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac J:53585, J:103489 View
Denys-Drash syndrome Wt1tm1Mlh/Wt1+ involves: 129P2/OlaHsd * C57BL/6 J:135449 View
Denys-Drash syndrome Wt1tm1Mlh/Wt1+ involves: 129P2/OlaHsd * C57BL/6 * MF1 J:135449 View
Denys-Drash syndrome Wt1tm1.1Lahe/Wt1+ involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL J:154995 View
Denys-Drash syndrome Wt1tm1Vih/Wt1+ involves: 129S7/SvEvBrd * C57BL/6 * MF1 J:94225 View
developmental and epileptic encephalopathy 7 Kcnq2tm1.1Lvi/Kcnq2+ 129-Kcnq2tm1.1Lvi/Lvi J:298666 View
developmental and epileptic encephalopathy 16 Tbc1d24em2Tbf/Tbc1d24em2Tbf C57BL/6J-Tbc1d24em2Tbf J:273646 View
developmental and epileptic encephalopathy 17 Gnao1tm2Rneu/Gnao1+ B6.129S1-Gnao1tm2Rneu J:271137 View
developmental and epileptic encephalopathy 17 Gnao1tm2.1Rneu/Gnao1+ B6.129S-Gnao1tm2.1Rneu J:216850 View
developmental and epileptic encephalopathy 17 Gnao1em1Rneu/Gnao1+ involves: C57BL/6J * C57BL/6NCrl J:271137 View
developmental and epileptic encephalopathy 39 Slc25a12Gt(OST123999)Lex/Slc25a12Gt(OST123999)Lex involves: 129S5/SvEvBrd * C57BL/6 J:243212 View
Diamond-Blackfan anemia 7 Ndor1Tg(UBC-cre/ERT2)1Ejb/Ndor1+
Rpl11tm1.1Srn/Rpl11+
involves: 129S6/SvEvTac * C57BL/6NCrl * CD-1 J:292575 View
diastrophic dysplasia Slc26a2tm1Aros/Slc26a2tm1Aros involves: 129S7/SvEvBrd * C57BL/6J J:97104 View
dicarboxylic aminoaciduria Slc1a1tm1Wst/Slc1a1tm1Wst involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:41613 View
DiGeorge syndrome Tbx1tm1Dsr/Tbx1tm1Dsr either: 129/Sv or (involves: 129/Sv * C57BL/6) J:93588 View
DiGeorge syndrome Tbx1tm1Dsr/Tbx1+ either: 129/Sv or (involves: 129/Sv * C57BL/6) J:93588 View
DiGeorge syndrome Tbx1tm1.1Dsr/Tbx1tm1.1Dsr either: 129/Sv or (involves: 129/Sv * C57BL/6) J:93588 View
DiGeorge syndrome Tbx1tm1.1Dsr/Tbx1+ either: 129/Sv or (involves: 129/Sv * C57BL/6) J:93588 View
DiGeorge syndrome Tbx1tm1Pa/Tbx1tm1Pa either: (involves: 129) or (involves: 129 * C57BL/6) or (involves: 129 * C57BL/6 * Swiss Webster) J:70730 View
DiGeorge syndrome Tbx1tm1Bem/Tbx1tm1Bem FVB.Cg-Tbx1tm1Bem J:91664 View
DiGeorge syndrome Tbx1tm1Bem/Tbx1+ FVB.Cg-Tbx1tm1Bem J:91664 View
DiGeorge syndrome Kat6atm1Avo/Kat6a+
Tbx1tm1Bld/Tbx1+
involves: 129 * 129S7/SvEvBrd * BALB/c * C57BL/6 J:188772 View
DiGeorge syndrome Tbx1tm2.1Bem/Tbx1tm2.2Bem
Foxg1tm1(cre)Skm/Foxg1+
involves: 129 * C57BL/6J * SJL * Swiss Webster J:105980, J:109536 View
DiGeorge syndrome Tbx1tm1Bem/Tbx1+ involves: 129/Sv * C57BL/6J * SJL J:67796 View
DiGeorge syndrome Tbx1tm1Pa/Tbx1+ involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ J:70730 View
DiGeorge syndrome Tbx1tm1Pa/Tbx1tm1Pa involves: 129S1/Sv * 129X1/SvJ J:94411 View
DiGeorge syndrome Tbx1tm1Pa/Tbx1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * Swiss Webster J:70730 View
DiGeorge syndrome Tbx1tm1Bld/Tbx1tm1Bld involves: 129S7/SvEvBrd * C57BL/6 J:67409 View
DiGeorge syndrome Tbx1tm1Bld/Tbx1tm2Bld involves: 129S7/SvEvBrd * C57BL/6 J:91013 View
DiGeorge syndrome Tbx1tm1Bld/Tbx1tm3Bld
Tg(Myh6-cre)2182Mds/0
involves: 129S7/SvEvBrd * C57BL/6 J:91013 View
DiGeorge syndrome Tbx1tm1Bld/Tbx1tm3Bld
Tg(Tek-cre)1Ywa/0
involves: 129S7/SvEvBrd * C57BL/6 J:91013 View
DiGeorge syndrome Tbx1tm1Bld/Tbx1+ involves: 129S7/SvEvBrd * C57BL/6 J:67409 View
DiGeorge syndrome Nkx2-5tm1(cre)Rjs/Nkx2-5+
Tbx1tm1Bld/Tbx1tm3Bld
involves: 129S7/SvEvBrd * C57BL/6 J:91013 View
DiGeorge syndrome Tbx1tm2Bld/Tbx1tm2Bld involves: 129S7/SvEvBrd * C57BL/6 J:91013 View
DiGeorge syndrome Tbx1tm2Bld/Tbx1+ involves: 129S7/SvEvBrd * C57BL/6 J:91013 View
dilated cardiomyopathy 1A Lmnatm2.1Gbon/Lmna+ involves: 129 * C57BL/6 J:198526 View
dilated cardiomyopathy 1A Lmnatm1Stw/Lmnatm1Stw involves: 129S1/Sv J:87613, J:131905 View
dilated cardiomyopathy 1A Lmnatm3Stw/Lmnatm3Stw involves: 129S1/Sv * 129S4/SvJaeSor * C57BL J:100393 View
dilated cardiomyopathy 1A Lmnatm1Gbon/Lmnatm1Gbon involves: 129S2/SvPas * C57BL/6 J:187399 View
dilated cardiomyopathy 1A Tg(Myh6-LMNA*E82K)35Lizh/0 involves: C57BL/6J J:167734 View
dilated cardiomyopathy 1C Ldb3tm4Chen/Ldb3tm4Chen
Myl2tm1(cre)Krc/Myl2+
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss J:144739 View
dilated cardiomyopathy 1C Ldb3tm4Chen/Ldb3tm4Chen
A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
involves: 129S1/Sv * 129X1/SvJ * Black Swiss * FVB/N J:144739 View
dilated cardiomyopathy 1C Tg(Myh6-LDB3*S196L)93Mva/0 involves: C57BL/6J J:243711 View
dilated cardiomyopathy 1CC Nexnem1Chen/Nexnem1Chen C57BL/6J-Nexnem1Chen J:301807 View
dilated cardiomyopathy 1CC Nexntm1Chen/Nexntm1Chen
Tg(Tnnt2-cre)5Blh/0
involves: C57BL/6 * DBA/2 J:290931 View
dilated cardiomyopathy 1CC Nexntm1Chen/Nexntm1Chen
Tg(myl2-cre)1118Tmhn/0
involves: MF1 J:290931 View
dilated cardiomyopathy 1CC Nexntm1.1Chen/Nexntm1.1Chen Not Specified J:290931 View
dilated cardiomyopathy 1D Tnnt2tm2.1Feah/Tnnt2+ involves: 129S6/SvEvTac * FVB/N J:243725 View
dilated cardiomyopathy 1D Tnnt2tm2Mmto/Tnnt2tm2Mmto involves: 129S/SvEv * C57BL/6 J:137784 View
dilated cardiomyopathy 1D Tnnt2tm2Mmto/Tnnt2+ involves: 129S/SvEv * C57BL/6 J:137784 View
dilated cardiomyopathy 1D Tg(Myh6-TNNT2*R141W)#Ajm/0 involves: C3H * C57BL/6 * ICR J:161899 View
dilated cardiomyopathy 1D Tg(Myh6-TNNT2*R141W)#Lian/0 involves: C57BL/6J J:211769 View
dilated cardiomyopathy 1DD Rbm20em1Hgra/Rbm20em1Hgra C57BL/6-Rbm20em1Hgra J:324088 View
dilated cardiomyopathy 1DD Rbm20em1Hgra/Rbm20+ C57BL/6-Rbm20em1Hgra J:324088 View
dilated cardiomyopathy 1DD Rbm20em1Hide/Rbm20em1Hide involves: C57BL/6J J:297234 View
dilated cardiomyopathy 1HH Bag3tm1c(EUCOMM)Hmgu/Bag3tm1.1Chen
Tg(Myhca-cre)1Abel/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * FVB/N J:246352 View
dilated cardiomyopathy 1HH Bag3tm1c(EUCOMM)Hmgu/Bag3tm1c(EUCOMM)Hmgu
Tg(Myhca-cre)1Abel/0
involves: C57BL/6N * FVB/N J:246352 View
dilated cardiomyopathy 1R Tg(Myh6-Actc1*R312H)307Iko/? involves: C57BL/6 J:178587 View
dilated cardiomyopathy 1R Tg(Myh6-ACTC1*E361G)361.20Sbm/0 Not Specified J:242344 View
dilated cardiomyopathy 1Y Tg(Myh6-Tpm1*D230N)HJcf/0 B6.FVB-Tg(Myh6-Tpm1*D230N)HJcf J:243724 View
dilated cardiomyopathy 1Y Tg(Myh6-Tpm1*E54K)30Dfw/0 involves: FVB/N J:137813 View
dilated cardiomyopathy 1Y Tg(Myh6-Tpm1*E54K)67Dfw/0 involves: FVB/N J:137813 View
distal hereditary motor neuronopathy type 2A Hspb8tm1Vti/Hspb8tm1Vti involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl J:284796 View
distal spinal muscular atrophy 1 Ighmbp2nmd-2J/Ighmbp2nmd-2J B6.BKS-Ighmbp2nmd-2J/J J:92862 View
distal spinal muscular atrophy 1 Ighmbp2em1Cll/Ighmbp2em1Cll FVB/NJ-Ighmbp2em1Cll J:326540 View
DNA ligase IV deficiency Lig4tiny/Lig4tiny C57BL/6-Lig4tiny J:122725 View
DNA ligase IV deficiency Lig4tm2.1Fwa/Lig4tm2.1Fwa involves: 129S6/SvEvTac J:157574 View
Donnai-Barrow syndrome Lrp2m267Asp/Lrp2m267Asp involves: C57BL/6J * FVB/N J:166387 View
Doyne honeycomb retinal dystrophy Efemp1tm1Eap/Efemp1tm1Eap involves: 129S6/SvEvTac * C57BL/6 * FVB/N J:129901 View
Doyne honeycomb retinal dystrophy Efemp1tm1Eap/Efemp1+ involves: 129S6/SvEvTac * C57BL/6 * FVB/N J:129901 View
Doyne honeycomb retinal dystrophy Efemp1tm1Lmar/Efemp1tm1Lmar involves: 129X1/SvJ * BALB/c J:129902 View
Doyne honeycomb retinal dystrophy Efemp1tm1Lmar/Efemp1+ involves: 129X1/SvJ * BALB/c J:129902 View
Dravet syndrome Scn1atm1Kea/Scn1a+ (C57BL/6J x 129S6/SvEvTac-Scn1atm1Kea)F1 J:203040 View
Dravet syndrome Scn1atm1Wac/Scn1a+ B6.129-Scn1atm1Wac J:113149, J:188126 View
Dravet syndrome Scn1atm1.1Kzy/Scn1a+ involves: 129P2/OlaHsd * C3HeB/FeJ J:260796 View
Dravet syndrome Scn1atm2.1Kzy/Scn1atm2.1Kzy
Tg(Pvalb-cre)1Tama/0
involves: 129P2/OlaHsd * C57BL/6 * DBA J:202863 View
Dravet syndrome Scn1atm2.1Kzy/Scn1a+
Tg(Pvalb-cre)1Tama/0
involves: 129P2/OlaHsd * C57BL/6 * DBA J:202863 View
Dravet syndrome Scn1atm1Wac/Scn1a+ involves: 129S1/Sv * 129X1/SvJ * FVB/NJ J:129998 View
Dravet syndrome Scn1atm2.1Wac/Scn1a+
Tg(I12b-cre)1Jlr/0
involves: 129X1/SvJ * C57BL/6J J:188126 View
Dravet syndrome Scn1atm2.1Wac/Scn1a+
Tg(I12b-cre)1Jlr/0
involves: C57BL/6J * CD-1 J:189897 View
Duane-radial ray syndrome Sall4Gt(XE027)Byg/Sall4+ B6;129P2-Sall4Gt(XE027)Byg J:105332 View
Duane-radial ray syndrome Sall4Gt(XE027)Byg/Sall4+ involves: 129P2/OlaHsd * Black Swiss * C57BL/6 J:105332 View
Duane-radial ray syndrome Sall4tm1Ryn/Sall4+ involves: 129P2/OlaHsd * C57BL/6J J:118119 View
Duane-radial ray syndrome Sall4tm1Brd/Sall4+ involves: 129S7/SvEvBrd * C57BL/6J J:117866 View
EAST syndrome Kcnj10tm1Lst/Kcnj10tm1Lst involves: 129S1/Sv J:226598 View
EAST syndrome Kcnj10tm1Lst/Kcnj10tm1Lst involves: 129S1/Sv * C57BL/6J J:77663 View
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 Trp63tm1Fmc/Trp63tm1Fmc involves: 129S4/SvJae J:54637 View
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 Trp63tm3Aam/Trp63+ involves: 129S7/SvEvBrd J:294158 View
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 Trp63tm1Brd/Trp63tm1Brd involves: 129S7/SvEvBrd * C57BL/6J J:54636 View
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 Trp63tm2Brd/Trp63tm2Brd involves: 129S7/SvEvBrd * C57BL/6J J:54636 View
Ehlers-Danlos syndrome classic type 1 Col5a1em1Brle/Col5a1+ C57BL/6-Col5a1em1Brle J:326524 View
Ehlers-Danlos syndrome classic type 1 Col5a1tm1Rjw/Col5a1+ either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6) J:113133 View
Ehlers-Danlos syndrome classic type 1 Col5a1tm1Rjw/Col5a1+ involves: 129S6/SvEvTac * C57BL/6 J:112728, J:326524 View
Ellis-Van Creveld syndrome Evctm1Jago/Evctm1Jago involves: 129S7/SvEvBrd * C57BL/6 J:124105 View
Ellis-Van Creveld syndrome Evc2tm1.1Mis/Evc2tm1.1Mis involves: 129X1/SvJ * C57BL/6 J:226455 View
endocrine-cerebro-osteodysplasia syndrome Cilk1tm1.1Zfu/Cilk1tm1.1Zfu B6.Cg-Cilk1tm1.1Zfu J:309653, J:309376 View
endocrine-cerebro-osteodysplasia syndrome Cilk1tm1a(KOMP)Mbp/Cilk1tm1a(KOMP)Mbp C57BL/6N-Cilk1tm1a(KOMP)Mbp J:211652 View
enhanced S-cone syndrome Nr2e3rd7/Nr2e3rd7 B6.Cg-Nr2e3rd7/J J:107820 View
enhanced S-cone syndrome Nr2e3rd7/Nr2e3rd7 Not Specified J:62171 View
epidermolysis bullosa simplex Ogna type Plectm7.1Gwi/Plectm7.1Gwi involves: 129P2/OlaHsd * C57BL/6 J:179812 View
epidermolysis bullosa simplex Ogna type Plectm7.1Gwi/Plec+ involves: 129P2/OlaHsd * C57BL/6 J:179812 View
epidermolysis bullosa simplex Ogna type Plectm1Gwi/Plectm1Gwi involves: 129S1/Sv * 129X1/SvJ J:59000 View
epidermolysis bullosa simplex Ogna type Plectm2Gwi/Plectm2Gwi involves: 129S1/Sv * 129X1/SvJ J:59000 View
epidermolysis bullosa simplex with muscular dystrophy Plectm1Gwi/Plectm1Gwi involves: 129S1/Sv * 129X1/SvJ J:59000 View
epidermolysis bullosa simplex with muscular dystrophy Plectm2Gwi/Plectm2Gwi involves: 129S1/Sv * 129X1/SvJ J:59000 View
episodic kinesigenic dyskinesia 1 Prrt2tm1d(KOMP)Wtsi/Prrt2tm1d(KOMP)Wtsi B6(Cg)-Prrt2tm1d(KOMP)Wtsi J:299667 View
episodic kinesigenic dyskinesia 1 Prrt2tm1d(KOMP)Wtsi/Prrt2+ B6(Cg)-Prrt2tm1d(KOMP)Wtsi J:299667 View
factor XI deficiency F11tm1Gjb/F11tm1Gjb involves: 129X1/SvJ * C57BL/6 J:40270 View
factor XII deficiency F12tm1Pbfd/F12tm1Pbfd B6.Cg-F12tm1Pbfd J:100529 View
factor XIII deficiency F13a1tm1Gdi/F13a1tm1Gdi involves: 129P2/OlaHsd J:86919 View
factor XIII deficiency F13a1tm1Gdi/F13a1tm1Gdi involves: 129P2/OlaHsd * CBA/Ca J:87293 View
familial cold autoinflammatory syndrome 1 Nlrp3tm2Hhf/Nlrp3+
Lyz2tm1(cre)Ifo/Lyz2+
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 J:150054 View
familial cold autoinflammatory syndrome 1 Nlrp3tm2Hhf/Nlrp3+
Tg(CAG-cre/Esr1*)5Amc/?
involves: 129/Sv * C57BL/6 * CBA J:150054 View
familial cold autoinflammatory syndrome 4 Tg(Cd74-Nlrc4*)1Kyas/0 involves: C57BL/6N J:219652 View
familial encephalopathy with neuroserpin inclusion bodies Serpini1tm1Dpw/Serpini1tm1Dpw involves: 129/Sv * C57BL/6JBom J:84427 View
familial encephalopathy with neuroserpin inclusion bodies Tg(Thy1-SERPINI1*G392E)333Icka/0 involves: C57BL * CD-1 * DBA J:144649 View
familial encephalopathy with neuroserpin inclusion bodies Tg(Thy1-SERPINI1*G392E)333Icka/Tg(Thy1-SERPINI1*G392E)333Icka involves: C57BL * CD-1 * DBA J:144649 View
familial episodic pain syndrome 3 Scn11aem1Akoi/Scn11a+ involves: C57BL/6 J:268684 View
familial erythrocytosis 2 Vhltm1Mcs/Vhltm1Mcs involves: 129S4/SvJae * C57BL/6 * FVB/N J:130780 View
familial hemophagocytic lymphohistiocytosis 2 Prf1tm1Sdz/Prf1tm1Sdz C57BL/6-Prf1tm1Sdz/J J:92260, J:193137 View
familial hemophagocytic lymphohistiocytosis 3 Unc13dJinx/Unc13dJinx C57BL/6J-Unc13dJinx/Mmucd J:119974 View
familial hemophagocytic lymphohistiocytosis 4 Stx11tm1.2Ics/Stx11tm1.2Ics involves: C57BL/6NTac J:193137 View
familial hypocalciuric hypercalcemia 1 CasrBCH002/CasrBCH002 C3HeB/FeJ-CasrBCH002 J:183993 View
familial hypocalciuric hypercalcemia 1 CasrBCH003/CasrBCH003 C3HeB/FeJ-CasrBCH003 J:183993 View
familial hypocalciuric hypercalcemia 1 CasrBCH004/CasrBCH004 C3HeB/FeJ-CasrBCH004 J:183993 View
familial hypocalciuric hypercalcemia 1 CasrBCH007/CasrBCH007 C3HeB/FeJ-CasrBCH007 J:183993 View
familial hypocalciuric hypercalcemia 1 CasrBCH011/CasrBCH011 C3HeB/FeJ-CasrBCH011 J:183993 View
familial hypocalciuric hypercalcemia 1 CasrBCH013/CasrBCH013 C3HeB/FeJ-CasrBCH013 J:183993 View
familial hypocalciuric hypercalcemia 1 Casrtm1Ces/Casr+ involves: 129X1/SvJ * Black Swiss J:29900 View
familial lipoprotein lipase deficiency Lpltm1Sem/Lpltm1Sem involves: 129P2/OlaHsd * C57BL/6J J:25652 View
familial lipoprotein lipase deficiency Lpltm1Sem/Lpl+ involves: 129P2/OlaHsd * C57BL/6J J:25652 View
familial lipoprotein lipase deficiency Lpltm1Bres/Lpltm1Bres involves: 129S4/SvJae * C57BL/6J J:30062 View
familial lipoprotein lipase deficiency Lpltm1Bres/Lpl+ involves: 129S4/SvJae * C57BL/6J J:30062 View
familial Mediterranean fever Mefvtm3.1(MEFV)Chae/Mefvtm3.1(MEFV)Chae B6.129S6-Mefvtm3.1(MEFV)Chae J:172117 View
familial Mediterranean fever Mefvtm4.1(MEFV)Chae/Mefvtm4.1(MEFV)Chae B6.129S6-Mefvtm4.1(MEFV)Chae J:172117 View
familial Mediterranean fever Mefvtm5.1(MEFV)Chae/Mefvtm5.1(MEFV)Chae B6.129S6-Mefvtm5.1(MEFV)Chae J:172117 View
familial Mediterranean fever Mefvtm1Chae/Mefvtm1Chae either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6) J:82763 View
familial temporal lobe epilepsy 1 Lgi1tm1.1Jkc/Lgi1tm1.1Jkc
Tyrc-Brd/Tyrc-Brd
B6.Cg-Tyrc-Brd Lgi1tm1.1Jkc J:158715 View
familial temporal lobe epilepsy 1 Lgi1tm1.1Ics/Lgi1tm1.1Ics involves: 129S2/SvPas * BALB/c * C57BL/6 J:182795 View
familial temporal lobe epilepsy 1 Lgi1tm1Mafu/Lgi1tm1Mafu involves: 129S6/SvEvTac * C57BL/6 J:157578 View
familial temporal lobe epilepsy 1 Tg(Lgi1*)#Mpan/0 Not Specified J:154129 View
Fanconi anemia complementation group A Fancatm1Faw/Fancatm1Faw involves: 129P2/OlaHsd * FVB J:63742 View
Fanconi anemia complementation group A Fancatm1Wong/Fancatm1Wong involves: C57BL/6 J:85108 View
Fanconi anemia complementation group A Fancatm1.1Wong/Fancatm1.1Wong involves: C57BL/6 J:85108 View
Fanconi anemia complementation group C Fancctm1Mab/Fancctm1Mab involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:32080 View
Fanconi anemia complementation group C Fancctm1Mgo/Fancctm1Mgo involves: 129S4/SvJaeSor * C57BL/6 J:61512 View
Fanconi anemia complementation group D1 Brca2tm1Kamc/Brca2tm1Kamc involves: 129P2/OlaHsd * BALB/c J:144998 View
Fanconi anemia complementation group D2 Fancd2tm1Hou/Fancd2tm1Hou 129S4/SvJae-Fancd2tm1Hou J:84892 View
Fanconi anemia complementation group D2 Fancd2tm1Hou/Fancd2tm1Hou B6.129S4-Fancd2tm1Hou J:84892 View
Fanconi anemia complementation group D2 Fancd2em1Tzh/Fancd2em1Tzh C57BL/6-Fancd2em1Tzh J:284566 View
Fanconi anemia complementation group D2 Fancd2tm1Hou/Fancd2tm1Hou involves: 129S4/SvJae * C57BL/6J J:84892 View
Fanconi anemia complementation group D2 Aldh2tm1a(EUCOMM)Wtsi/Aldh2tm1a(EUCOMM)Wtsi
Fancd2tm1Hou/Fancd2tm1Hou
involves: 129S4/SvJae * C57BL/6J * C57BL/6N J:193232 View
Fanconi anemia complementation group D2 Fancd2Gt(OST57859)Lex/Fancd2Gt(OST57859)Lex
Usp1tm1.1Ada/Usp1tm1.1Ada
involves: 129S5/SvEvBrd * C57BL/6 J:146616 View
fetal encasement syndrome Chuktm1Aki/Chuktm1Aki involves: 129P2/OlaHsd J:195185 View
fetal encasement syndrome Chuktm1Mka/Chuktm1Mka involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA J:195185 View
fetal encasement syndrome Chuktm1Ver/Chuktm1Ver involves: 129S4/SvJae * C57BL/6J J:195185 View
fibrodysplasia ossificans progressiva Acvr1tm1Emsh/Acvr1+ chimera involves: BALB/c * C57BL/6 * CD-1 J:194134 View
fibrodysplasia ossificans progressiva Acvr1tm2.1Vlcg/Acvr1+
Gt(ROSA)26Sortm3.1(cre/ERT2)Vlcg/Gt(ROSA)26Sor+
involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6NTac J:234069 View
fibrodysplasia ossificans progressiva Acvr1tm1Glh/Acvr1+
Gt(ROSA)26Sortm1.2(CAG-EGFP)Glh/Gt(ROSA)26Sor+
Tg(Pdgfra-cre)1Clc/0
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * FVB/N J:257905 View
fibrodysplasia ossificans progressiva Acvr1tm1Glh/Acvr1+
Gt(ROSA)26Sortm1.2(CAG-EGFP)Glh/Gt(ROSA)26Sor+
Tg(Tek-cre)1Ywa/0
involves: 129S6/SvEvTac * C57BL/6J * FVB/N * SJL J:257905 View
fibrodysplasia ossificans progressiva Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis/0 involves: C57BL/6 * DBA/2 J:142253 View
fibrodysplasia ossificans progressiva Acvr1tm2.1Vlcg/Acvr1+
Tg(Prrx1-cre)1Cjt/0
involves: C57BL/6J * C57BL/6NTac * SJL/J J:239136 View
fibular hypoplasia and complex brachydactyly Gdf5Bp-5J/Gdf5+ C57BL/6J-Gdf5Bp-5J/GrsrJ J:200816 View
focal segmental glomerulosclerosis 1 Actn4tm1Plk/Actn4tm1Plk involves: 129 * C57BL/6 J:83911 View
focal segmental glomerulosclerosis 2 Tg(NPHS2-Trpc6)F419Walz/0 involves: C57BL/6J * CBA/J J:165112 View
focal segmental glomerulosclerosis 2 Tg(NPHS2-Trpc6*P111Q)F615Walz/0 involves: C57BL/6J * CBA/J J:165112 View
focal segmental glomerulosclerosis 2 Tg(NPHS2-Trpc6*E896K)F75aWalz/0 involves: C57BL/6J * CBA/J J:165112 View
focal segmental glomerulosclerosis 3 Cd2apem1Irgu/Cd2apem1Irgu C57BL/6-Cd2apem1Irgu J:294238 View
Friedreich ataxia Fxntm1.1Pand/Fxntm1Mkn B6.Cg-Fxntm1.1Pand Fxntm1Mkn/J J:242978 View
Friedreich ataxia Fxntm2Mkn/Fxntm2.1Mkn
Tg(Ckmm-cre)1Lrsn/0
involves: 129 * C57BL/6J J:75420 View
Friedreich ataxia Fxntm2Mkn/Fxntm2.1Mkn
Tg(Eno2-cre)39Jme/0
involves: 129 * C57BL/6J J:75420 View
Friedreich ataxia Fxntm1Mkn/Fxntm1Pand involves: 129/Sv * C57BL/6 J:216422 View
Friedreich ataxia Fxntm1Mkn/Fxntm1Mkn
Tg(FXN)YG8Pook/0
involves: 129/Sv * C57BL/6 * CBA J:114840, J:216422 View
Friedreich ataxia Fxntm1Mkn/Fxntm1Mkn
Tg(FXN)YG22Pook/0
involves: 129/Sv * C57BL/6 * CBA J:114840 View
frontonasal dysplasia 3 Alx1em1Jian/Alx1em1Jian C57BL/6N-Alx1em1Jian J:320497 View
Fuhrmann syndrome Wnt7apx-2J/Wnt7apx-2J B6;C3Fe-Wnt7apx-2J/GrsrJ J:188478 View
Fuhrmann syndrome Wnt7apx-J/Wnt7apx-J C57BL/6J-Wnt7apx-J/GrsrJ J:188477 View
Fukuyama congenital muscular dystrophy Fktntm1Ttd/Fktntm2(FCMD)Ttd involves: 129S7/SvEvBrd J:144746 View
Fukuyama congenital muscular dystrophy Fktntm1Ttd/Fktntm1Ttd involves: 129S7/SvEvBrd * C57BL/6 J:97950 View
Fukuyama congenital muscular dystrophy Dysfim/Dysfim
Fktntm1Ttd/Fktntm2(FCMD)Ttd
involves: 129S7/SvEvBrd * C57BL/6 * SJL/J J:221523 View
Fukuyama congenital muscular dystrophy Fktntm1Kcam/Fktntm1Kcam
Myf5tm3(cre)Sor/Myf5+
involves: 129S/SvEv * 129S4/SvJaeSor J:187144 View
Fukuyama congenital muscular dystrophy Fktntm1Kcam/Fktntm1Kcam
Tg(CAG-cre/Esr1*)5Amc/?
involves: 129S/SvEv * C57BL/6 * CBA J:187144 View
Fukuyama congenital muscular dystrophy Fktntm1Kcam/Fktntm1Kcam
Tg(Ckmm-cre)5Khn/?
involves: 129S/SvEv * FVB J:187144 View
geleophysic dysplasia 1 Adamtsl2tm1c(KOMP)Wtsi/Adamtsl2tm1c(KOMP)Wtsi
Tg(Prrx1-cre)1Cjt/0
B6.Cg-Adamtsl2tm1c(KOMP)Wtsi Tg(Prrx1-cre)1Cjt J:280264 View
giant axonal neuropathy 1 Gantm1Jpj/Gantm1Jpj involves: C57BL/6 J:140136 View
giant axonal neuropathy 1 Gantm1Yany/Gantm1Yany Not Specified J:103926, J:108239 View
Gitelman syndrome Slc12a3tm1Ges/Slc12a3tm1Ges Not Specified J:50596 View
glutaric acidemia I Gcdhtm1Dmk/Gcdhtm1Dmk involves: 129S4/SvJae * C57BL/6J J:77874 View
glutaric acidemia I Gcdhtm1Dmk/Gcdhtm1Dmk involves: 129S4/SvJae * C57BL/6N * FVB/N J:256227 View
glutaric acidemia type 3 Sugcttm1.2Kald/Sugcttm1.2Kald B6.Cg-Sugcttm1.2Kald J:293423 View
glycogen storage disease III Agltm1Geno/Agltm1Geno C57BL/6J-Agltm1Geno J:218471 View
glycogen storage disease III Agltm1a(EUCOMM)Wtsi/Agltm1a(EUCOMM)Wtsi involves: C57BL/6N J:212003 View
glycogen storage disease V Pygmtm1.1Adru/Pygmtm1.1Adru involves: 129 * C57BL/6J J:226312 View
glycogen storage disease XV Gygtm1a(KOMP)Wtsi/Gygtm1a(KOMP)Wtsi involves: C57BL/6N J:300001 View
GM1 gangliosidosis Glb1tm1Adz/Glb1tm1Adz involves: 129/Sv * C57BL/6 J:98543 View
GM1 gangliosidosis Glb1tm1Adz/Glb1tm1Adz involves: 129P2/OlaHsd J:38620 View
GM1 gangliosidosis Glb1tm1Jmat/Glb1tm1Jmat involves: C57BL/6 * CBA * ICR J:40522, J:43534 View
GM2 gangliosidosis, AB variant Gm2atm1Rlp/Gm2atm1Rlp involves: 129S4/SvJae * C57BL/6 J:41950 View
gnathodiaphyseal dysplasia Ano5em1Huyi/Ano5em1Huyi C57BL/6N-Ano5em1Huyi J:294237 View
Goldberg-Shprintzen syndrome Kifbpem1Hmy/Kifbpem1Hmy Not Specified J:253679 View
Goldberg-Shprintzen syndrome Kifbpem2Hmy/Kifbpem2Hmy Not Specified J:253679 View
GRACILE syndrome Bcs1ltm1.1Levp/Bcs1ltm1.1Levp involves: 129 * 129S6/SvEvTac * C57BL/6 J:189652 View
gray platelet syndrome Nbeal2gps/Nbeal2gps 129S1/SvImJ-Nbeal2gps J:236370 View
gray platelet syndrome Nbeal2tm1a(EUCOMM)Wtsi/Nbeal2tm1a(EUCOMM)Wtsi C57BL/6N-Nbeal2tm1a(EUCOMM)Wtsi/Wtsi J:220801 View
gray platelet syndrome Nbeal2tm1Lex/Nbeal2tm1Lex involves: 129S5/SvEvBrd * C57BL/6J J:201413 View
Greig cephalopolysyndactyly syndrome Gli3Xt-J/Gli3Xt-J involves: C3H * CD-1 J:4086 View
Griscelli syndrome type 1 Myo5ad-n/Myo5ad-n B10.D2-H2d/nSnJ J:171603 View
Griscelli syndrome type 1 Myo5ad-l34J/Myo5ad-l34J BALB/cJ-Myo5ad-l34J/GrsrJ J:216055 View
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Grntm2.1Far/Grntm2.1Far involves: 129S4/SvJae * C57BL/6 J:259651 View
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Grntm1.1Far/Grntm1.1Far involves: 129S4/SvJae * C57BL/6J * FVB/N J:218705 View
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Grntm1.1Hiok/Grn+ involves: C57BL/6J J:259943 View
Hajdu-Cheney syndrome Notch2tm1.1Ecan/Notch2+ involves: 129 * 129S1/Sv * C57BL/6J J:230045 View
Hajdu-Cheney syndrome Notch2tm1.1Hhtg/Notch2+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:311038 View
Hajdu-Cheney syndrome Notch2tm2.2Ecan/Notch2+ involves: 129S1/Sv * C57BL/6J J:246017 View
Hajdu-Cheney syndrome Notch2tm2.1Ecan/Notch2tm2.1Ecan
Tg(BGLAP-cre)1Clem/0
involves: C57BL/6J * FVB/NJ J:246017 View
hand-foot-genital syndrome Hoxa13Hd/Hoxa13Hd B6C3Fe-a/a Hoxa13Hd Mcoln3Va-J/J J:58731 View
hand-foot-genital syndrome Hoxa13Hd/Hoxa13+ B6C3Fe-a/a Hoxa13Hd Mcoln3Va-J/J J:54823 View
hand-foot-genital syndrome Hoxa13tm1Jwi/Hoxa13tm1Jwi involves: 129S7/SvEvBrd J:94412 View
hand-foot-genital syndrome Hoxa13tm1Jwi/Hoxa13+ involves: 129S7/SvEvBrd J:94412 View
hand-foot-genital syndrome Hoxa13Hd/Hoxa13Hd involves: MYA/Hu J:64253, J:5211 View
hereditary hemorrhagic telangiectasia Engtm1Hma/Eng+ 129P2/OlaHsd-Engtm1Hma J:73415 View
hereditary hemorrhagic telangiectasia Engtm1Mle/Eng+ 129P2/OlaHsd-Engtm1Mle J:58502 View
hereditary hemorrhagic telangiectasia Acvrl1tm2.1Spo/Acvrl1tm2.1Spo
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
involves: 129 * 129S1/Sv * 129X1/SvJ J:154620 View
hereditary hemorrhagic telangiectasia Acvrl1tm2Spo/Acvrl1tm2Spo
Tg(Acvrl1-cre)L1Spo/0
involves: 129 * 129S4/SvJae * C57BL/6 * FVB/N J:130020 View
hereditary hemorrhagic telangiectasia Acvrl1tm2.1Spo/Acvrl1tm2.1Spo
Tg(Tal1-cre/ERT)1Jrg/0
involves: 129 * C57BL/6 J:227170 View
hereditary hemorrhagic telangiectasia Acvrl1tm2.1Spo/Acvrl1tm2.1Spo
Tg(Acvrl1-cre)L1Spo/0
involves: 129 * FVB J:154620 View
hereditary hemorrhagic telangiectasia Engtm2.1Hma/Engtm2.1Hma
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ J:212952, J:227170 View
hereditary hemorrhagic telangiectasia Engtm1Mle/Eng+ involves: 129P2/OlaHsd * C57BL/6 J:58502 View
hereditary hemorrhagic telangiectasia Engtm2.1Hma/Engtm2.1Hma
Tg(Tagln-cre)1Her/0
involves: 129P2/OlaHsd * C57BL/6 * SJL J:212952 View
hereditary hemorrhagic telangiectasia Engtm1Dyl/Engtm1Dyl involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:55403 View
hereditary hemorrhagic telangiectasia Acvrl1tm1Enl/Acvrl1+ involves: C57BL/6 J:82115 View
hereditary multiple exostoses Ext1tm1Vcs/Ext1tm1Vcs
Tg(Col2a1-rtTA,tetO-cre)22Pjro/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:157599 View
hereditary multiple exostoses Ext1tm1.1Vcs/Ext1tm1.1Vcs
Tg(Col2a1-rtTA,tetO-cre)22Pjro/0
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL J:157599 View
hereditary multiple exostoses Ext1tm1.1Vcs/Ext1tm1.1Vcs
Tg(Col2a1-cre/ERT)KA3Smac/0
involves: 129S1/Sv * 129X1/SvJ * FVB/N J:242977 View
hereditary multiple exostoses Ext1tm1Yama/Ext1tm1Yama
Acantm1(cre/ERT2)Crm/Acan+
involves: 129S5/SvEvBrd * 129S6/SvEvTac * C57BL/6NCrl J:242977 View
hereditary multiple exostoses Ext1tm1Yama/Ext1tm1Yama
Tg(Col2a1-cre/ERT)KA3Smac/0
involves: 129S5/SvEvBrd * FVB/N J:161395 View
hereditary neuropathy with liability to pressure palsies Pmp22Tr-2J/Pmp22+ C57BL/6J-Pmp22Tr-2J/GrsrJ J:201866 View
hereditary neuropathy with liability to pressure palsies Pmp22tm1Ueli/Pmp22tm1Ueli involves: 129S/SvEv J:29517 View
hereditary neuropathy with liability to pressure palsies Pmp22tm1Lnot/Pmp22+ Not Specified J:104989 View
hereditary neutrophilia Csf3rtm1Eur/Csf3rtm1Eur involves: 129P2/OlaHsd * C57BL/6 * FVB J:48503 View
hereditary sensory and autonomic neuropathy type 6 Dstdt-23Rbrc/Dstdt-23Rbrc involves: C3H/HeN * C57BL/6 J:251779 View
hereditary spastic paraplegia 4 SpastM1Gri/SpastM1Gri B6.C-SpastM1Gri J:148877 View
hereditary spastic paraplegia 4 Spasttm1.1Evre/Spasttm1.1Evre C57BL/6-Spasttm1.1Evre J:253467 View
hereditary spastic paraplegia 4 Spasttm1.1Jme/Spasttm1.1Jme involves: C57BL/6J J:117740 View
hereditary spastic paraplegia 4 Gt(ROSA)26Sortm1.1(CAG-SPAST*C448Y)Baas/Gt(ROSA)26Sortm1.1(CAG-SPAST*C448Y)Baas involves: C57BL/6N J:273408 View
hereditary spastic paraplegia 4 Gt(ROSA)26Sortm1.1(CAG-SPAST*C448Y)Baas/Gt(ROSA)26Sor+ involves: C57BL/6N J:273408 View
hereditary spastic paraplegia 7 Spg7tm1Eir/Spg7tm1Eir either: 129/Sv-Spg7tm1Eir or (involves: 129/Sv * C57BL/6) J:87616 View
hereditary spastic paraplegia 11 Spg11Gt(EUCE0085f05)Hmgu/Spg11Gt(EUCE0085f05)Hmgu involves: 129P2/OlaHsd * C57BL/6 J:228803 View
hereditary spastic paraplegia 13 Hspd1Gt(OST171441)Lex/Hspd1+ B6.129S5-Hspd1Gt(OST171441)Lex J:197946 View
hereditary spastic paraplegia 15 Zfyve26tm1.1Cahb/Zfyve26tm1.1Cahb involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 J:223127 View
hereditary spastic paraplegia 30 Kif1algdg/Kif1algdg C3.Cg-Kif1algdg/GrsrJ J:229662 View
hereditary spastic paraplegia 30 Kif1algdg-2J/Kif1algdg-2J C57BL/6J-Kif1algdg-2J/CxJ J:229662 View
hereditary spastic paraplegia 31 Reep1Gt(OST398247)Tigm/Reep1Gt(OST398247)Tigm B6J.Cg-Reep1Gt(OST398247)Tigm J:239250 View
hereditary spastic paraplegia 35 Fa2htm1.1Hama/Fa2htm1.1Hama involves: 129 * C57BL/6 J:171655 View
hereditary spastic paraplegia 48 Ap5z1tm1(KOMP)Wtsi/Ap5z1tm1(KOMP)Wtsi involves: 129 * C57BL/6N J:283611 View
hereditary spastic paraplegia 54 Ddhd2tm1Crv/Ddhd2tm1Crv involves: C57BL/6 J:216446 View
hereditary spherocytosis type 1 Ank1pale/Ank1pale C57BL/6J-Ank1pale/GrsrJ J:222308 View
hereditary spherocytosis type 1 Ank1nb/Ank1nb either: (involves: non-inbred stock) or (involves: C57BL/6) or (involves: WB/Re) J:11441 View
hereditary spherocytosis type 1 Ank1Rbc2/Ank1Rbc2 involves: 129S1/Sv * BALB/c J:148127 View
hereditary spherocytosis type 1 Ank1M1Wlst/Ank1M1Wlst involves: 129S1/SvImJ * C3H/HeJ * C57BL/6 J:170562 View
hereditary spherocytosis type 3 Spta1sph/Spta1sph either: (B6.C3-Spta1sph x WB.C3-Spta1sph)F1 or (WB.C3-Spta1sph x B6.C3-Spta1sph)F1 J:6695 View
hereditary spherocytosis type 3 Spta1sph/Spta1sph involves: C3H J:12276 View
hereditary spherocytosis type 3 Spta1sph-ha/Spta1sph-ha involves: DBA/1J J:14946, J:30699 View
hereditary spherocytosis type 3 Spta1ihj/Spta1ihj involves: HRS/J * LAH J:157766 View
hereditary spherocytosis type 3 Spta1sph-2Bc/Spta1sph-2Bc involves: SELH J:7048, J:7501 View
hereditary spherocytosis type 4 Slc4a1wan/Slc4a1wan C3H/HeJ-Slc4a1wan/J J:89043 View
Hermansky-Pudlak syndrome Bloc1s5mu/Bloc1s5mu CHMU/Le J:29151, J:75830 View
Hermansky-Pudlak syndrome Bloc1s5mu/Bloc1s5mu involves: Stock t J:29151 View
Hermansky-Pudlak syndrome 1 Hps1ep/Hps1ep B6.C3Fe-Hps1ep/J J:80751 View
Hermansky-Pudlak syndrome 1 Hps1ep-7J/Hps1ep-7J CAST/EiJ-Hps1ep-7J/GrsrJ J:198843 View
Hermansky-Pudlak syndrome 1 Ap3b1pe/Ap3b1pe
Hps1ep/Hps1ep
involves: C3H/He * C3HeB/FeJ * C57BL/6J J:85431 View
Hermansky-Pudlak syndrome 1 Hps1ep/Hps1ep involves: C3HeB/FeJ * C57BL/6J J:7416 View
Hermansky-Pudlak syndrome 2 Ap3b1pe/Ap3b1pe B6.C3-Ap3b1pe/J J:221384 View
Hermansky-Pudlak syndrome 2 Ap3b1pe-rim2/Ap3b1pe-rim2 involves: B10.A(R201) * C57BL/10Slc J:42685 View
Hermansky-Pudlak syndrome 2 Ap3b1pe/Ap3b1pe involves: C3H/He J:52879, J:80751 View
Hermansky-Pudlak syndrome 2 Ap3b1pe/Ap3b1pe
Hps1ep/Hps1ep
involves: C3H/He * C3HeB/FeJ * C57BL/6J J:85431 View
Hermansky-Pudlak syndrome 3 Hps3coa-6J/Hps3coa-6J C3H/HeJ-Hps3coa-6J/J J:63693 View
Hermansky-Pudlak syndrome 3 Hps3coa/Hps3coa involves: C57BL/10J J:9300, J:80751 View
Hermansky-Pudlak syndrome 3 Hps3coa/Hps3coa
Myo5ad/Myo5ad
Mregdsu/Mregdsu
involves: C57BL/10J J:29467 View
Hermansky-Pudlak syndrome 4 Hps4le/Hps4le B6.C3-Pde6brd1 Hps4le J:75144 View
Hermansky-Pudlak syndrome 4 Hps4le/Hps4le
Pde6brd1/Pde6brd1
B6.C3-Pde6brd1 Hps4le/J J:221384 View
Hermansky-Pudlak syndrome 5 Hps5ru2-J/Hps5ru2-J C57BL/6J-Hps5ru2-J/J J:81444 View
Hermansky-Pudlak syndrome 5 Hps5ru2/Hps5ru2 involves: C57BL J:81444 View
Hermansky-Pudlak syndrome 5 Hps5ru2-hz/Hps5ru2-hz involves: DBA/2J J:81444 View
Hermansky-Pudlak syndrome 6 a/a
Hps6ru/Hps6ru
B6.Cg-Hps6ru J:81444 View
Hermansky-Pudlak syndrome 6 Hps6ru-6J/Hps6ru-6J involves: C3H/HeJ J:81444 View
Hermansky-Pudlak syndrome 7 Dtnbp1sdy/Dtnbp1sdy involves: DBA/2J J:1958, J:85123 View
Hermansky-Pudlak syndrome 8 Bloc1s3rp/Bloc1s3rp involves: C57BL/10ScSn * C57BL/Tb J:80751 View
Hermansky-Pudlak syndrome 9 Bloc1s6pa/Bloc1s6pa B6.Cg-Bloc1s6pa/J J:221384 View
holoprosencephaly 2 Six3tm1Gco/Six3tm1Gco involves: 129S1/Sv J:81797 View
holoprosencephaly 2 Six3tm3.1Gco/Six3+
Shhtm1Chg/Shh+
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:140315 View
holoprosencephaly 2 Six3tm3Gco/Six3tm3Gco
Foxg1tm1(cre)Skm/Foxg1+
involves: 129S1/Sv * C57BL/6 J:140315 View
holoprosencephaly 2 Six3tm4(cre/ERT2)Gco/Six3+ involves: 129S1/Sv * C57BL/6 J:140315 View
holoprosencephaly 3 Shhtm1Chg/Shhtm1Chg involves: 129S1/Sv * 129X1/SvJ J:35802 View
holoprosencephaly 3 Disp1icb/Disp1tm1Amc
Shhtm1Amc/Shh+
involves: 129X1/SvJ * C57BL/6J J:92058 View
holoprosencephaly 3 Shhtm1Chg/Shhtm1Chg involves: C57BL/6 J:89364 View
holoprosencephaly 5 Zic2Ku/Zic2Ku 129S.CAnNCrl(C3)-Zic2Ku J:238567 View
holoprosencephaly 5 Zic2Ku/Zic2Ku C3.CAnNCrl-Zic2Ku J:138862 View
holoprosencephaly 5 Zic2tm1Jaru/Zic2tm1Jaru involves: 129S4/SvJae * C57BL/6 J:60644 View
holoprosencephaly 11 Boctm1Rsk/Boctm1Rsk
Cdontm1Rsk/Cdontm1Rsk
B6.129-Boctm1Rsk Cdontm1Rsk J:171767 View
holoprosencephaly 11 Boctm2Rsk/Boctm2Rsk
Cdontm1Rsk/Cdontm1Rsk
B6.129-Boctm2Rsk Cdontm1Rsk J:171767 View
holoprosencephaly 11 Boctm1Rsk/Boctm1Rsk
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac J:171767 View
holoprosencephaly 11 Boctm1Rsk/Boc+
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac J:171767 View
holoprosencephaly 11 Boctm2Rsk/Boctm2Rsk
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac J:171767 View
holoprosencephaly 11 Boctm2Rsk/Boc+
Cdontm1Rsk/Cdontm1Rsk
involves: 129/Sv * 129S6/SvEvTac J:171767 View
holoprosencephaly 11 Cdontm1Rsk/Cdontm1Rsk involves: 129/Sv * C57BL/6 J:82221 View
holoprosencephaly 11 Cdontm2Rsk/Cdontm2Rsk involves: 129/Sv * C57BL/6 J:82221 View
Holt-Oram syndrome Tbx5tm1.1Jse/Tbx5+ either: (involves: 129/Sv) or (involves: Black Swiss) J:92050, J:112887 View
Holt-Oram syndrome Tbx5tm1.1Jse/Tbx5+ involves: 129/Sv * Black Swiss J:71845 View
Holt-Oram syndrome Tbx5tm1Jse/Tbx5+ involves: 129S/SvEv J:112887 View
hyper IgE recurrent infection syndrome 1 Tg(Stat3*)9199Alau/0 involves: C57BL/6 J:210877 View
hyperekplexia 1 Glra1tm1Betz/Glra1tm1Betz B6.129P2-Glra1tm1Betz J:117236 View
hyperekplexia 1 Glra1spd-ot9J/Glra1spd-ot9J B6.Cg-Glra1spd-ot9J/GrsrJ J:234690 View
hyperekplexia 1 Glra1tm1Rah/Glra1+ involves: 129X1/SvJ * C57BL/6J J:85341 View
hyperekplexia 1 Glra1spd/Glra1spd involves: A/HeJ J:33924 View
hyperekplexia 1 Tg(Thy1-GLRA1*R271Q)300Wha/0 involves: C57BL/6 * DBA/2 J:76009 View
hyperekplexia 1 Tg(Thy1-GLRA1*R271Q)382Wha/Tg(Thy1-GLRA1*R271Q)382Wha involves: C57BL/6 * DBA/2 J:76009 View
hyperekplexia 2 Glrbspa/Glrbspa Not Specified J:33924 View
hyperekplexia 3 Slc6a5trsl/Slc6a5trsl C57BL/6J-Slc6a5trsl/GrsrJ J:235637 View
hyperekplexia 3 Slc6a5tm1Betz/Slc6a5tm1Betz involves: 129P2/OlaHsd J:86625 View
hypogonadotropic hypogonadism 7 with or without anosmia Gnrhrhh/Gnrhrhh involves: 129S6/SvEvTac * C57BL/6 J:96941 View
hypogonadotropic hypogonadism 8 with or without anosmia Kiss1rtm1Gstn/Kiss1rtm1Gstn involves: 129P2/OlaHsd J:102113 View
hypogonadotropic hypogonadism 8 with or without anosmia Kiss1rtm1Rla/Kiss1rtm1Rla involves: 129S1/SvImJ J:126704 View
hypogonadotropic hypogonadism 8 with or without anosmia Kiss1rtm1.1Lex/Kiss1rtm1.1Lex involves: 129S4/SvJae J:181650 View
hypogonadotropic hypogonadism 8 with or without anosmia Kiss1rtm1Coll/Kiss1rtm1Coll involves: 129S6/SvEvTac J:96442 View
hypogonadotropic hypogonadism 11 with or without anosmia Tacr3tm1Jasi/Tacr3tm1Jasi involves: 129P2/OlaHsd * C57BL/6 J:182547 View
hypogonadotropic hypogonadism 12 with or without anosmia Gnrh1hpg/Gnrh1hpg involves: 101/H * C3H/HeH J:5877 View
hypogonadotropic hypogonadism 13 with or without anosmia Kiss1tm1Rla/Kiss1tm1Rla involves: 129S1/SvImJ J:126704 View
hypogonadotropic hypogonadism 13 with or without anosmia Kiss1tm1Coll/Kiss1tm1Coll involves: 129S/SvEv * 129S6/SvEvTac J:122381 View
hypomyelinating leukodystrophy 2 Gjb1tm1Kwi/Y
Gjc2tm1(EGFP)Kwi/Gjc2tm1(EGFP)Kwi
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 J:219594 View
hypomyelinating leukodystrophy 2 Gjc2tm1(EGFP)Kwi/Gjc2tm1(EGFP)Kwi
Gjb1tm1Kwi/Gjb1tm1Kwi
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 J:219594 View
hypomyelinating leukodystrophy 2 Gjc2tm2.1Kwi/Gjc2tm2.1Kwi involves: C57BL/6 * SJL J:174197 View
hypomyelinating leukodystrophy 6 Tubb4aJit/Tubb4aJit FVB.B6-Tubb4aJit J:321692 View
hypomyelinating leukodystrophy 6 Tubb4aJit/Tubb4a+ FVB.B6-Tubb4aJit J:321692 View
hypomyelinating leukodystrophy 6 Tubb4aem1Avan/Tubb4aem1Avan involves: C57BL/6 J:291062 View
hypotrichosis 6 Dsg4hage/Dsg4hage
Faslpr/Faslpr
X/Yaa
EOD-Dsg4hage J:140028 View
hypotrichosis 6 Dsg4lah-J/Dsg4lah-J involves: DBA/1LacJ J:83117 View
hypotrichosis 6 Dsg4lah/Dsg4lah LAH/Pas J:33849 View
hypotrichosis 13 Krt71Ca-19J/Krt71+ BALB/cJ-Krt71Ca-19J/GrsrJ J:213988 View
immunodeficiency 15A Ikbkbem1Macc/Ikbkbem1Macc involves: C57BL/6NCrl J:290616 View
immunodeficiency 15A Ikbkbem1Macc/Ikbkb+ involves: C57BL/6NCrl J:290616 View
immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia Rac2em1Shl/Rac2+ involves: C57BL/6 J:276213 View
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Dnmt3atm1Enl/Dnmt3atm1Enl
Dnmt3btm1Enl/Dnmt3btm1Enl
involves: 129S4/SvJae * C57BL/6 J:58298 View
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Dnmt3btm1Enl/Dnmt3btm1Enl involves: 129S4/SvJae * C57BL/6 J:58298 View
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Dnmt3btm1Enl/Dnmt3btm6Enl involves: 129S4/SvJae * C57BL/6 J:106540 View
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Dnmt3btm1Enl/Dnmt3btm7Enl involves: 129S4/SvJae * C57BL/6 J:106540 View
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Dnmt3btm6Enl/Dnmt3btm6Enl involves: 129S4/SvJae * C57BL/6 J:106540 View
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Dnmt3btm6Enl/Dnmt3btm7Enl involves: 129S4/SvJae * C57BL/6 J:106540 View
immunodeficiency-centromeric instability-facial anomalies syndrome 1 Dnmt3btm7Enl/Dnmt3btm7Enl involves: 129S4/SvJae * C57BL/6 J:106540 View
infantile hypophosphatasia Alpltm1Jlm/Alpltm1Jlm either: (involves: 129S2/SvPas) or (involves: 129S2/SvPas * C57BL/6J) J:39015 View
infantile hypophosphatasia Alpltm1Sor/Alpltm1Sor either: (involves: 129S7/SvEvBrd-Alpltm1Sor) or (involves: 129S7/SvEvBrd * C57BL/6) J:28394 View
infantile hypophosphatasia Alpltm1Jlm/Alpltm1Jlm involves: 129S1/SvImJ * 129S2/SvPas * C57BL/6 J:233260 View
isolated microphthalmia 6 Prss56glcr4/Prss56glcr4 C3A.Cg-Prss56glcr4 Pde6b+ J:188765 View
isolated microphthalmia 6 Prss56glcr4/Prss56glcr4 C57BL/6J-Prss56glcr4 J:188765 View
isolated microphthalmia 6 Prss56glcr4/Prss56glcr4 involves: C3H/HeA * C57BL/6J * C57BL/LiA J:188765 View
Johanson-Blizzard syndrome Ubr1tm1Avar/Ubr1tm1Avar involves: 129S1/Sv * C57BL/6 J:105229 View
junctional epidermolysis bullosa with pyloric atresia Itgb4tm1Fgg/Itgb4tm1Fgg involves: 129S1/Sv * C57BL/6 J:48924 View
juvenile polyposis syndrome Smad4tm1Mmt/Smad4+ B6.129S2-Smad4tm1Mmt J:59214 View
juvenile polyposis syndrome Tg(CAG-Bmpr1a*,-lacZ)1Nobs/0
Tg(Mpz-cre)94Imeg/0
involves: 129X1/SvJ * C57BL/6J J:192670 View
karyomegalic interstitial nephritis Fan1tm1a(KOMP)Wtsi/Fan1tm1a(KOMP)Wtsi 129S1.B6-Fan1tm1a(KOMP)Wtsi J:242198 View
karyomegalic interstitial nephritis Fan1tm1.1Jrou/Fan1tm1.1Jrou involves: 129P2/OlaHsd J:232403 View
karyomegalic interstitial nephritis Fan1tm1d(KOMP)Wtsi/Fan1tm1d(KOMP)Wtsi involves: C57BL/6N * FVB/N J:232402 View
Kaufman oculocerebrofacial syndrome Ube3btm1a(EUCOMM)Hmgu/Ube3btm1a(EUCOMM)Hmgu C57BL/6-Ube3btm1a(EUCOMM)Hmgu J:273879 View
KINSSHIP syndrome Aff3tm1a(EUCOMM)Wtsi/Aff3tm1a(EUCOMM)Wtsi C57BL/6N-Aff3tm1a(EUCOMM)Wtsi/Wtsi J:317476 View
Kleefstra syndrome 1 Ehmt1tm1.1Tara/Ehmt1tm1.1Tara
Tg(Camk2a-cre)2Gsc/0
involves: 129P2/OlaHsd * C57BL/6 * FVB/N J:155739 View
Kleefstra syndrome 1 Ehmt1tm1Yshk/Ehmt1+ involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj J:157021, J:192316 View
Kufor-Rakeb syndrome Atp13a2tm1.2Wtd/Atp13a2tm1.2Wtd involves: 129 * C57BL/6 J:221680 View
LADD syndrome Fgf10tm1Wss/Fgf10+ involves: 129X1/SvJ J:237227 View
Lafora disease Tg(CAG-EPM2A*C266S)1Bmin/0 involves: 129 * C57BL/6 * SJL J:262504, J:120356 View
Lafora disease Epm2atm1Kzy/Epm2atm1Kzy involves: 129P2/OlaHsd * C57BL/6J J:76688, J:173769 View
Lafora disease Nhlrc1tm1.2Geno/Nhlrc1tm1.2Geno involves: 129S2/SvPas * C57BL/6J J:181559 View
Lafora disease Nhlrc1tm1Bmin/Nhlrc1tm1Bmin involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr J:181674 View
Lafora disease Nhlrc1tm1(KOMP)Vlcg/Nhlrc1tm1(KOMP)Vlcg involves: C57BL/6J * C57BL/6NTac J:165994, J:218959 View
Laron syndrome Ghrtm1Jjk/Ghrtm1Jjk involves: 129P2/OlaHsd * BALB/c J:44604, J:157146 View
Laron syndrome Ghrtm1Arge/Ghrtm1Arge involves: 129S/SvEv * C57BL/6J J:66913 View
Leber congenital amaurosis 1 Gucy2ecpfl9/Gucy2ecpfl9 B6;129P2-Gucy2ecpfl9/Boc J:269362 View
Leber congenital amaurosis 1 Gucy2etm1Gar/Gucy2etm1Gar
Nrltm1Asw/Nrltm1Asw
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 J:241970 View
Leber congenital amaurosis 1 Gucy2etm1Gar/Gucy2etm1Gar
Gucy2ftm1Wbae/Gucy2ftm1Wbae
involves: 129S6/SvEvTac J:120903 View
Leber congenital amaurosis 2 Rpe65rd12/Rpe65rd12 B6(A)-Rpe65rd12/J J:104929 View
Leber congenital amaurosis 2 Rpe65tm1Tmr/Rpe65tm1Tmr involves: 129S1/Sv * 129X1/SvJ J:136882 View
Leber congenital amaurosis 2 Rpe65tm1Tmr/Rpe65tm1Tmr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:51293, J:61889, J:71529, J:81027, J:85796 View
Leber congenital amaurosis 2 Cnga3tm1Biel/Cnga3tm1Biel
Rpe65tm1Tmr/Rpe65tm1Tmr
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:71529 View
Leber congenital amaurosis 4 Aipl1tvrm119/Aipl1tvrm119 C57BL/6J-Aipl1tvrm119/Pjn J:243745 View
Leber congenital amaurosis 4 Aipl1tvrm127/Aipl1tvrm127 C57BL/6J-Aipl1tvrm127/Pjn J:243745 View
Leber congenital amaurosis 4 Aipl1tm1Visu/Aipl1tm1Visu involves: 129S1/Sv * 129X1/SvJ * C57BL/6J J:92617 View
Leber congenital amaurosis 4 Aipl1tm1Tili/Aipl1tm1Tili involves: 129S4/SvJae * C57BL/6 J:92601 View
Leber congenital amaurosis 4 Aipl1tm1Mad/Aipl1tm1Mad involves: 129S7/SvEvBrd J:94655 View
Leber congenital amaurosis 5 Lca5Gt(AG0283)Wtsi/Lca5Gt(AG0283)Wtsi involves: 129P2/OlaHsd * C57BL/6 J:174018 View
Leber congenital amaurosis 6 Rpgrip1nmf247/Rpgrip1nmf247 C57BL/6J-Rpgrip1nmf247 J:243745 View
Leber congenital amaurosis 6 Rpgrip1tvrm111/Rpgrip1tvrm111 C57BL/6J-Rpgrip1tvrm111/Pjn J:243745 View
Leber congenital amaurosis 6 Rpgrip1tm1Tili/Rpgrip1tm1Tili involves: 129S4/SvJae * C57BL/6 J:82755 View
Leber congenital amaurosis 8 Crb1tm1Wij/Crb1tm1Wij
Crb2tm1.1Wij/Crb2tm1.1Wij
Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL J:207895 View
Leber congenital amaurosis 8 Crb1tm1Wij/Crb1+
Crb2tm1.1Wij/Crb2tm1.1Wij
Tg(Chx10-EGFP/cre,-ALPP)2Clc/0
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JOlaHsd * SJL J:207895 View
Leber congenital amaurosis 8 Crb1rd8/Crb1rd8 STOCK Crb1rd8/J J:171736 View
Leber congenital amaurosis 9 Nmnat1imh/Nmnat1imh B6J.C(C3H)-Nmnat1imh J:234111 View
Leber congenital amaurosis 9 Nmnat1tm1Ruch/Nmnat1tm1d(EUCOMM)Wtsi involves: 129S1/Sv * 129S7/SvEvBrd * C57BL/6J * C57BL/6N J:267630 View
Leber congenital amaurosis 12 Rd3rd3/Rd3rd3 RBF/DnJ-Rd3rd3 J:202634 View
Leber congenital amaurosis 14 Lrattm1Kpal/Lrattm1Kpal involves: 129S6/SvEvTac J:136882 View
leukocyte adhesion deficiency 1 Itgb2tm1Bay/Itgb2tm1Bay involves: 129S7/SvEvBrd J:13599 View
leukocyte adhesion deficiency 1 Itgb2tm1Bay/Itgb2tm1Bay involves: 129S7/SvEvBrd * C57BL/6J J:13599 View
leukocyte adhesion deficiency 1 Itgb2tm2Bay/Itgb2tm2Bay involves: 129S7/SvEvBrd * C57BL/6J J:48542 View
leukocyte adhesion deficiency 3 Fermt3tm1Ref/Fermt3tm1Ref involves: 129S1/Sv * 129X1/SvJ J:146783 View
Li-Fraumeni syndrome Trp53tm3.1Glo/Trp53+ B6.129S7-Trp53tm3.1Glo J:95318 View
Li-Fraumeni syndrome Trp53tm1Tyj/Trp53tm1Tyj involves: 129S2/SvPas J:95316 View
Li-Fraumeni syndrome Trp53tm1Tyj/Trp53+ involves: 129S2/SvPas J:95316 View
Li-Fraumeni syndrome Trp53tm1Tyj/Trp53tm2.1Tyj involves: 129S2/SvPas * 129S4/SvJae J:95316 View
Li-Fraumeni syndrome Trp53tm1Tyj/Trp53tm3.1Tyj involves: 129S2/SvPas * 129S4/SvJae J:95316 View
Li-Fraumeni syndrome Trp53tm1Tyj/Trp53+ involves: 129S2/SvPas * C57BL/6 J:17728 View
Li-Fraumeni syndrome Trp53tm2.1Tyj/Trp53+ involves: 129S4/SvJae J:95316 View
Li-Fraumeni syndrome Trp53tm3.1Tyj/Trp53+ involves: 129S4/SvJae J:95316 View
long QT syndrome 1 Kcnq1tm3Kpfe/Kcnq1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N J:93197 View
long QT syndrome 1 Tg(Myh6-KCNQ1_i2)H02Desc/0 involves: FVB J:132483 View
long QT syndrome 1 Tg(Myh6-KCNQ1_i2)H05Desc/0 involves: FVB J:211437 View
long QT syndrome 3 Scn5atm1Care/Scn5a+ FVB.129P2-Scn5atm1Care/Care J:128657 View
long QT syndrome 3 Scn5atm1.1Iba/Scn5a+ involves: 129 * C57BL/6 J:266290 View
long QT syndrome 3 Scn5atm1Clhh/Scn5a+ involves: 129/SvEv J:186583 View
long QT syndrome 3 Scn5atm1Pec/Scn5a+ involves: Swiss J:71542 View
Lynch syndrome Msh2tm1Rak/Msh2tm2.1Rak
Tg(Vil1-cre)20Syr/0
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * DBA/2 * SJL J:161577 View
Lynch syndrome Msh2tm2.1Rak/Msh2tm3.1Rak
Tg(Vil1-cre)20Syr/0
involves: 129/Sv * C57BL/6 * DBA/2 * SJL J:161577 View
Lynch syndrome Msh2tm2.1Rak/Msh2tm2.1Rak
Tg(Vil1-cre)20Syr/0
involves: 129/Sv * C57BL/6 * FVB/N * SJL J:161577 View
Lynch syndrome Msh2tm1Htr/Msh2tm1Htr involves: 129P2/OlaHsd J:45433 View
Lynch syndrome Msh2tm1Htr/Msh2tm1Htr
Tap1tm1Hpl/Tap1tm1Hpl
involves: 129P2/OlaHsd * FVB J:45433 View
macrocephaly-autism syndrome Ptentm2Mak/Ptentm2Mak
Tg(Eno2-cre)39Jme/0
involves: 129P2/OlaHsd * C57BL/6 * SJL J:109635 View
macrocephaly-autism syndrome Ptentm1Engc/Ptentm1Engc involves: CD-1 J:210487 View
Mahvash Disease Gcgrem2Smoc/Gcgrem2Smoc C57BL/6J-Gcgrem2Smoc J:300368 View
malignant hyperthermia Ryr1tm3.1Alle/Ryr1tm3.1Alle involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6 J:303297 View
malignant hyperthermia Ryr1tm3.1Alle/Ryr1+ involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6 J:303297 View
malignant hyperthermia Ryr1tm2.1Alle/Ryr1+ involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:168222 View
malignant hyperthermia Ryr1tm1Slh/Ryr1+ involves: 129S7/SvEvBrd * C57BL/6 J:105738 View
malignant hyperthermia Ryr1em1Tmur/Ryr1+ Not Specified J:322211 View
Marsili syndrome Zfhx2tm3Ymri/Zfhx2tm3Ymri involves: 129P2/OlaHsd * C57BL/6 J:266472 View
Marsili syndrome Tg(Zfhx2*R1907K)#Jcox/0 involves: C57BL/6 J:266472 View
maturity-onset diabetes of the young type 1 Hnf4atm1.1Gonz/Hnf4atm1.1Gonz
Tg(Ins2-cre)25Mgn/0
involves: 129X1/SvJ * C57BL/6 * DBA J:108652 View
maturity-onset diabetes of the young type 2 Gcktm2Mgn/Gcktm2Mgn 129S6/SvEvTac-Gcktm2Mgn J:121910 View
maturity-onset diabetes of the young type 2 Gcktm2Mgn/Gck+ 129S6/SvEvTac-Gcktm2Mgn J:121910 View
maturity-onset diabetes of the young type 2 Gcktm1Ts/Gcktm1Ts either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J) J:29255 View
maturity-onset diabetes of the young type 2 Gcktm1Ts/Gck+ either: (involves: 129S7/SvEvBrd * C57BL/6J) or (involves: 129S7/SvEvBrd * DBA/2J) J:29255 View
maturity-onset diabetes of the young type 2 Gcktm1Efr/Gck+ involves: 129P2/OlaHsd * C57BL/6 J:28756 View
maturity-onset diabetes of the young type 2 Gcktm1.2Mgn/Gcktm1.2Mgn involves: 129S6/SvEvTac * C57BL/6 J:51826 View
maturity-onset diabetes of the young type 2 Gcktm1.2Mgn/Gck+ involves: 129S6/SvEvTac * C57BL/6 J:51826 View
maturity-onset diabetes of the young type 2 Gcktm1.1Mgn/Gcktm1.1Mgn
Tg(Ins2-cre)25Mgn/0
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 J:51826 View
maturity-onset diabetes of the young type 2 Gcktm1.1Mgn/Gcktm1.1Mgn
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 J:51826 View
maturity-onset diabetes of the young type 2 Gcktm1.1Mgn/Gck+
Tg(Ins2-cre)25Mgn/0
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 J:51826 View
maturity-onset diabetes of the young type 2 Gcktm1Tka/Gck+ involves: 129X1/SvJ * ICR J:30334 View
maturity-onset diabetes of the young type 2 GckGena348/GckGena348 involves: BALB/c * C3H/He J:90389 View
maturity-onset diabetes of the young type 2 GckGena348/Gck+ involves: BALB/c * C3H/He J:90389 View
maturity-onset diabetes of the young type 2 Gckm1Rge/Gck+ involves: C3HeB/FeJ J:162903 View
maturity-onset diabetes of the young type 2 Gcktm1Hrt/Gck+
Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+
involves: C57BL/6 * DBA J:105247, J:250069 View
maturity-onset diabetes of the young type 2 GckRgsc210/GckRgsc210 involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc210/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc272/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc341/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc392/GckRgsc392 involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc392/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc475/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc702/GckRgsc702 involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc702/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc149/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc236/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc552/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc553/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 2 GckRgsc735/Gck+ involves: C57BL/6J * DBA/2J J:88919 View
maturity-onset diabetes of the young type 3 Hnf1atm1.1Ylee/Hnf1atm1.1Ylee involves: 129X1/SvJ * C57BL/6J J:47008 View
maturity-onset diabetes of the young type 3 Tg(Ins2-Hnf1a)#Cbw/0 involves: C57BL/6 * CBA/J J:134757 View
maturity-onset diabetes of the young type 3 Tg(Ins2-TCF1*P291)2Kya/0 involves: C57BL/6 * SJL J:73760 View
maturity-onset diabetes of the young type 4 Pdx1tm1Ted/Pdx1+ involves: 129P2/OlaHsd J:82969 View
mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations Mast1em1Dak/Mast1+ B6.Cg-Mast1em1Dak J:268904 View
megaconial type congenital muscular dystrophy Chkbrmd/Chkbrmd involves: BALB/cByJ * C57BL/6J J:108320 View
megalencephalic leukoencephalopathy with subcortical cysts 1 Mlc1tm1.1Vdk/Mlc1tm1.1Vdk involves: C57BL/6 J:250520, J:244698 View
microcephalic osteodysplastic primordial dwarfism type II PcntGt(RRU388)Byg/PcntGt(RRU388)Byg B6.129P2-PcntGt(RRU388)Byg J:226309 View
microphthalmia with limb anomalies Smoc1tm1a(EUCOMM)Wtsi/Smoc1tm1a(EUCOMM)Wtsi C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi J:174198 View
microphthalmia with limb anomalies Smoc1Tn(sb-lacZ,GFP)PV384Jtak/Smoc1Tn(sb-lacZ,GFP)PV384Jtak involves: C3H * C57BL/6J * DBA/2 J:169180 View
microvillus inclusion disease Myo5btm1a(KOMP)Wtsi/Myo5btm1a(KOMP)Wtsi C57BL/6N-Myo5btm1a(KOMP)Wtsi J:229427 View
microvillus inclusion disease Myo5btm1.1Cle/Myo5btm1.1Cle
Tg(Vil1-cre/ERT2)23Syr/0
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6 * DBA/2 J:227079 View
mitochondrial DNA depletion syndrome 2 Tk2tm1Mihi/Tk2tm1Mihi involves: 129S6/SvEv * C57BL/6J J:139195, J:166725 View
mitochondrial DNA depletion syndrome 5 Sucla2Gt(SAbetageo)1Bhg/Sucla2+ involves: 129S6/SvEvTac * C57BL/6 J:213453 View
mosaic variegated aneuploidy syndrome 1 Bub1btm2.1Jvd/Bub1b+ involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 J:194926 View
mosaic variegated aneuploidy syndrome 1 Bub1btm1Jvd/Bub1btm3.1Jvd involves: 129S6/SvEvTac * C57BL/6 J:293084 View
Mowat-Wilson syndrome Zeb2tm1.2Yhi/Zeb2tm1.2Yhi involves: 129S1/Sv * 129X1/SvJ * CD-1 J:82084 View
mucosulfatidosis Sumf1Gt(RST760)Byg/Sumf1Gt(RST760)Byg involves: 129P2/OlaHsd * C57BL/6 J:120146 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw 129S6.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3+ 129S6.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw B6.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3+ B6.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw CBACa.129P2-Fgfr3tm1.1Aomw J:144356 View
Muenke Syndrome Fgfr3tm1.1Aomw/Fgfr3+ CBACa.129P2-Fgfr3tm1.1Aomw J:144356 View
mulibrey nanism Trim37Gt(RRO307)Byg/Trim37Gt(RRO307)Byg B6J.129P2-Trim37Gt(RRO307)Byg J:232482 View
multicentric carpotarsal osteolysis syndrome Mafbem1Staka/Mafbem1Staka involves: C57BL/6J J:279108 View
multiple endocrine neoplasia type 1 Men1tm1Rvt/Men1+ involves: 129 * C57BL/6 J:191261 View
multiple endocrine neoplasia type 1 Men1tm1Zqw/Men1+ involves: 129/Sv * 129P2/OlaHsd J:85302 View
multiple endocrine neoplasia type 1 Men1tm1.2Zqw/Men1tm1.2Zqw
Tg(Ins2-cre)23Herr/0
involves: 129P2/OlaHsd * C57BL/6J * CBA/J J:85133 View
multiple endocrine neoplasia type 1 Men1tm1Ctre/Men1tm1Ctre
Tg(Pdx1-cre)89.1Dam/0
involves: 129S6/SvEvTac * C57BL/6 * CBA * FVB/N J:146440 View
multiple endocrine neoplasia type 1 Men1tm1.1Gfk/Men1+ involves: 129T2/SvEms * C57BL/6 J:116086 View
multiple endocrine neoplasia type 1 Men1tm2.1Gfk/Men1+ involves: 129T2/SvEms * C57BL/6 J:116086 View
multiple endocrine neoplasia type 1 Men1tm1Gfk/Men1tm1Gfk
Tg(Ins2-cre)25Mgn/0
involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA J:89898 View
multiple endocrine neoplasia type 2B Rettm2.1Cos/Rettm2.1Cos involves: 129S1/Sv * C57BL/6J * FVB/N J:60659 View
multiple endocrine neoplasia type 2B Rettm2.1Cos/Ret+ involves: 129S1/Sv * C57BL/6J * FVB/N J:60659 View
multiple epiphyseal dysplasia 5 Matn3tm1Mbri/Matn3tm1Mbri involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:125104 View
muscular dystrophy-dystroglycanopathy type B5 Fkrptm1Itl/Fkrptm1Itl involves: 129S6/SvEvTac * C57BL/6N J:164448 View
muscular dystrophy-dystroglycanopathy type B6 Large1myd-3J/Large1myd-3J STOCK Large1myd-3J/GrsrJ J:160357 View
myoclonic dystonia 11 Sgcetm1Ygl/Sgce+ involves: 129S2/SvPas J:180682 View
myoclonic dystonia 11 Sgcetm1Ygl/Sgcetm1Ygl involves: 129S2/SvPas * 129S4/SvJaeSor * BALB/c * C57BL/6 J:101332 View
myofibrillar myopathy 1 Destm1.1Ccrs/Destm1.1Ccrs involves: 129 * C57BL/6J J:219616 View
myofibrillar myopathy 1 Destm1.1Ccrs/Des+ involves: 129 * C57BL/6J J:219616 View
myofibrillar myopathy 1 Destm1Cap/Destm1Cap involves: 129S7/SvEvBrd * C57BL/6 J:35123 View
myofibrillar myopathy 1 Tg(Myh6-Des*)641Rbns/0 involves: FVB/N J:108730 View
myofibrillar myopathy 2 Tg(Myh6-Cryab*R120G)708Rbns/0 FVB/N-Tg(Myh6-Cryab*R120G)708Rbns J:133093 View
myofibrillar myopathy 2 Cryabtm1.1Ady/Cryabtm1.1Ady involves: 129X1/SvJ * C57BL/6 * C57BL/6J J:171679 View
myofibrillar myopathy 2 Cryabtm1.1Ady/Cryab+ involves: 129X1/SvJ * C57BL/6 * C57BL/6J J:171679 View
myofibrillar myopathy 2 Tg(Myh6-CRYAB*R120G)7302Ijb/0 involves: C57BL/6 J:126781 View
myofibrillar myopathy 5 Flnctm1.1Rsdf/Flnc+ involves: C57BL/6 J:226976 View
nail-patella syndrome Lmx1btm1Rjo/Lmx1btm1Rjo involves: 129 * C57BL/6 J:47316 View
nail-patella syndrome Lmx1btm1Rjo/Lmx1btm1Rjo involves: 129S7/SvEvBrd J:95961 View
nail-patella syndrome Lmx1btm1Rjo/Lmx1btm1Rjo involves: 129S7/SvEvBrd * C57BL/6 J:95961 View
nail-patella syndrome Lmx1btm4.1Rjo/Lmx1btm4.1Rjo
Tg(NPHS2-cre)295Lbh/0
involves: 129S7/SvEvBrd * C57BL/6 * SJL J:122505 View
Nasu-Hakola disease Tyrobptm1.1Viv/Tyrobptm1.1Viv B6.129P2-Tyrobptm1.1Viv J:95232 View
Nasu-Hakola disease Tyrobptm1Ttk/Tyrobptm1Ttk involves: 129P2/OlaHsd * C57BL/6 J:81823 View
nemaline myopathy 2 Nebm1Anu/Nebm2Anu C57BL/6J-Nebm1Anu Nebm2Anu J:285564 View
nemaline myopathy 2 Nebtm1Slbt/Nebtm1Slbt involves: 129P2/OlaHsd J:149329 View
nemaline myopathy 2 Nebtm2Hgra/Nebtm2Hgra
Tg(Ckmm-cre)5Khn/0
involves: 129S6/SvEvTac * FVB J:225840 View
nemaline myopathy 2 Nebtm1.1Hgra/Nebtm1.1Hgra involves: C57BL/6 * C57BL/6J * SJL J:206854 View
nemaline myopathy 3 Acta1tm1Hrd/Acta1+ either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6JArc) J:184588 View
nemaline myopathy 3 Acta1tm1Jll/Acta1+
Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno
involves: C57BL/6 * CBA J:209273 View
nemaline myopathy 3 Tg(ACTA1*D286G)#Kjno/Tg(ACTA1*D286G)#Kjno involves: C57BL/6 * CBA J:209273 View
nemaline myopathy 3 Tg(ACTA1*D286G/EGFP)#Kjno/0 involves: C57BL/6J * CBA/Ca J:182255 View
nemaline myopathy 5 Tnnt1tm1.2Jin/Tnnt1tm1.2Jin involves: 129P2/OlaHsd * C57BL/6 J:219907 View
nemaline myopathy 6 Kbtbd13em1Coeo/Kbtbd13em1Coeo involves: C57BL/6J J:295442 View
nemaline myopathy 8 Klhl40tm1(KOMP)Vlcg/Klhl40tm1(KOMP)Vlcg C57BL/6-Klhl40tm1(KOMP)Vlcg J:213780 View
nemaline myopathy 10 Lmod3em1Eno/Lmod3em1Eno involves: C3H * C57BL/6 J:222174 View
nemaline myopathy 10 Lmod3Tn(pb-Act-RFP)1.1Zhu/Lmod3Tn(pb-Act-RFP)1.1Zhu involves: C57BL/6J J:223382 View
nemaline myopathy 11 Mypntm1.1Epu/Mypntm1.1Epu involves: 129S6/SvEvTac J:248575 View
neonatal diabetes mellitus with congenital hypothyroidism Glis3tm1Amj/Glis3tm1Amj involves: 129 * C57BL/6 J:148994 View
neonatal diabetes mellitus with congenital hypothyroidism Glis3tm1Hiha/Glis3tm1Hiha involves: C57BL/6 * CBA J:150077 View
nephronophthisis 1 Nphp1em1Lisu/Nphp1em1Lisu C57BL/6J-Nphp1em1Lisu J:324503 View
nephronophthisis 2 Invsinv/Invsinv involves: FVB/N J:132552 View
nephronophthisis 3 Nphp3pcy/Nphp3tm1Cbe involves: C57BL/6 * CD-1 * KK/Upj J:139258 View
nephronophthisis 3 Nphp3pcy/Nphp3pcy involves: KK J:91453 View
nephronophthisis 4 Nphp4nmf192/Nphp4nmf192 involves: C57BL/6J J:167232 View
nephronophthisis 7 Glis2tm1Tre/Glis2tm1Tre B6.129P2-Glis2tm1Tre J:123510 View
Netherton syndrome F2rl1tm1Cgh/F2rl1tm1Cgh
Spink5tm1Hov/Spink5tm1Hov
involves: 129P2/OlaHsd * 129S4/SvJae J:180855 View
Netherton syndrome Spink5tm1Drh/Spink5tm1Drh involves: 129P2/OlaHsd * C57BL/6 J:95549 View
Netherton syndrome Spink5tm1Hov/Spink5tm1Hov involves: 129P2/OlaHsd * FVB J:96435 View
Netherton syndrome Spink5m1Btlr/Spink5m1Btlr involves: C57BL/6J J:183755 View
Netherton syndrome Spink5Tn(Pgk2-sb10,sb-Tyr)1498Ove/Spink5Tn(Pgk2-sb10,sb-Tyr)1498Ove involves: FVB/N J:93050 View
neurodegeneration with brain iron accumulation 2a Pla2g6m1J/Pla2g6m1J C3H/HeJ-Pla2g6m1J J:183152 View
neurodegeneration with brain iron accumulation 2a Pla2g6m1Sein/Pla2g6m1Sein C57BL/6JJcl-Pla2g6m1Sein J:155328 View
neurodegeneration with brain iron accumulation 2a Pla2g6tm1Tsu/Pla2g6tm1Tsu involves: 129S2/SvPas * C57BL/6 J:174587 View
neurodegeneration with brain iron accumulation 2a Pla2g6tm1Turk/Pla2g6tm1Turk involves: 129X1/SvJ J:131429 View
neurodegeneration with brain iron accumulation 6 Coasytm1.1Vtr/Coasytm1.1Vtr
Tg(Syn1-cre)671Jxm/0
involves: 129 * C57BL/6N * CBA J:299154 View
neurodevelopmental disorder with involuntary movements Gnao1em2Rneu/Gnao1+ C57BL/6J-Gnao1em2Rneu J:303229 View
neurodevelopmental disorder with midbrain and hindbrain malformations Arhgef2Gt(IST13976A8)Tigm/Arhgef2Gt(IST13976A8)Tigm involves: C57BL/6N J:242973 View
neurohypophyseal diabetes insipidus Avptm1Lja/Avp+ involves: 129S1/Sv * 129X1/SvJ J:148012