![]() ![]() |
||||||||
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 | 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 | ||||
aceruloplasminemia | Cptm1Yos/Cptm1Yos | C.129P2-Cptm1Yos | J:142713 | View | ||||
acheiropody | Lmbr1tm1Kng/Lmbr1tm1Kng | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * DBA/2J | J:72166 | 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 | Trip11m1Mawa/Trip11m1Mawa | C57BL/6J-Trip11m1Mawa | J:163656 | 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 | Cnga3cpfl5/Cnga3cpfl5 | involves: RHJ/LeJ | J:187090 | View | ||||
achromatopsia 2 | Cnga3tm1Biel/Cnga3tm1Biel | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:56020 | 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 | ||||
adrenoleukodystrophy | Abcd1tm1Kan/Abcd1tm1Kan | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:44812 | View | ||||
adrenoleukodystrophy | Abcd1tm1Kan/Y | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:44812 | View | ||||
adrenoleukodystrophy |
Abcd1tm1Kan/Y Gt(ROSA)26Sortm2.1(CAG-ELOVL1)Geno/Gt(ROSA)26Sor+ Cnptm1(cre)Kan/Cnp+ |
involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6J | J:257393 | View | ||||
adrenoleukodystrophy | Abcd1tm1Kds/Abcd1tm1Kds | either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6) | J:42479 | View | ||||
adrenoleukodystrophy | Abcd1tm1Kds/Abcd1tm1Kds | involves: 129/Sv * 129S4/SvJae * C57BL/6J | J:75388 | View | ||||
adrenoleukodystrophy | Abcd1tm1Kds/Y | either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129/Sv * 129S4/SvJae * C57BL/6) | J:42479 | View | ||||
adrenoleukodystrophy | Abcd1tm1Kds/Y | involves: 129S4/SvJae * C57BL/6J | J:94583 | View | ||||
adrenoleukodystrophy | Abcd1tm1Ymd/Abcd1tm1Ymd | involves: 129S/SvEv * C57BL/6J * DBA/2J | J:40230 | View | ||||
adrenoleukodystrophy | Abcd1tm1Ymd/Y | involves: 129S/SvEv * C57BL/6J * DBA/2J | J:40230 | View | ||||
adult hypophosphatasia | AlplBAP023/AlplBAP023 | C3HeB/FeJ-AlplBAP023 | J:183993 | View | ||||
adult hypophosphatasia | AlplHpp/Alpl+ | involves: BALB/cAnN * C3H/HeH | J:122319 | View | ||||
adult hypophosphatasia | AlplHpp/AlplHpp | involves: BALB/cAnN * C3H/HeH | J:122319 | 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-onset autosomal dominant demyelinating leukodystrophy | Tg(Lmnb1)1Yfu/0 | involves: C57BL/6J | J:197168 | View | ||||
advanced sleep phase syndrome 1 | Per2M1Btlr/Per2M1Btlr | C57BL/6J-Per2M1Btlr | J:264638 | 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 | Slc12a6tm1Dlp/Slc12a6tm1Dlp | involves: 129 * C57BL/6J | J:79870 | 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 | Slc12a6tm1Tjj/Slc12a6tm1Tjj | involves: 129/Sv * C57BL/6 | J:86183 | 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 | ||||
Aicardi-Goutieres syndrome | Adarem3Qwan/Adarem3Qwan | Not Specified | J:325221 | View | ||||
Aicardi-Goutieres syndrome | Trex1tm1Tld/Trex1tm1Tld | involves: 129P2/OlaHsd | J:145466 | View | ||||
alacrima, achalasia, and impaired intellectual development syndrome | Gmppatm1d(EUCOMM)Wtsi/Gmppatm1d(EUCOMM)Wtsi | involves: C57BL/6N | J:305791 | 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 | Gfaptm3Mes/Gfap+ | involves: 129S6/SvEvTac * 129S7/SvEvBrd * FVB/N | J:114689 | View | ||||
Allan-Herndon-Dudley syndrome | Slc16a2tm1Dgen/Y | either: (involves: C57BL/6N) or (involves: NMRI) | J:120737 | View | ||||
alopecia universalis | Hrrh-8J/Hrrh-8J | B10.D2/nSnJ-Hrrh-8J | J:50909 | View | ||||
alopecia universalis | Hrrh-Chr/Hrrh-Chr | Not Specified | J:53633 | View | ||||
alopecia universalis | Hrrhsl/Hrrhsl | involves: BALB/c | J:98859 | 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(Nes-cre)2472Pick/0 |
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-2-plasmin inhibitor deficiency | Serpinf2tm1Hrl/Serpinf2tm1Hrl | involves: 129X1/SvJ * C57BL/6J | J:54047, J:55243 | View | ||||
Alstrom syndrome | Alms1foz/Alms1foz | involves: NOD | J:107058 | 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 | 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 | ||||
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/Psen1tm1Mpm | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:51950 | View | ||||
Alzheimer's disease 3 | Psen1tm1Mpm/Psen1tm1Pcw | involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ * C57BL/6 | J:91277 | View | ||||
Alzheimer's disease 3 | Psen1tm1Shn/Psen1tm1Shn | involves: 129S7/SvEvBrd * C57BL/6 | J:40365 | View | ||||
Alzheimer's disease 3 | Psen1tm1Tak/Psen1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:108326 | 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 | 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/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 | Enamtm1.1Jcch/Enam+ | involves: C57BL/6 | J:223123 | View | ||||
amelogenesis imperfecta type 1B | Enamtm1.1Jcch/Enamtm1.1Jcch | involves: C57BL/6 | J:223123 | View | ||||
amelogenesis imperfecta type 1E | AmelxRgsc888/Amelx+ | involves: C57BL/6JJcl * DBA/2J | J:157947 | View | ||||
amelogenesis imperfecta type 1E | AmelxRgsc888/AmelxRgsc888 | involves: C57BL/6JJcl * DBA/2J | J:157947 | View | ||||
amelogenesis imperfecta type 1E | AmelxRgsc888/Y | involves: C57BL/6JJcl * DBA/2J | J:157947 | View | ||||
amelogenesis imperfecta type 1E | Amelxtm1Kul/Amelxtm1Kul | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:71126 | View | ||||
amelogenesis imperfecta type 1E |
Amelxtm1Kul/Amelxtm1Kul Tg(AMELX*P70T)2Gibs/? |
involves: 129S1/Sv * 129X1/SvJ | J:122914 | View | ||||
amelogenesis imperfecta type 1E | Tg(AMELX*P70T)2Gibs/? | Not Specified | J:122914 | View | ||||
amelogenesis imperfecta type 3C | Reltem1Jpsi/Reltem1Jpsi | C57BL/6-Reltem1Jpsi | J:279949 | View | ||||
amyotrophic lateral sclerosis type 1 | Sod1m1H/Sod1m1H | involves: C3H/HeH * C57BL/6J | J:219360 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Sod1*G86R)M1Jwg/0 | involves: FVB/N | J:22628, J:58733, J:91800 | View | ||||
ankyloblepharon-ectodermal defects-cleft lip/palate syndrome | Trp63tm1Cmis/Trp63+ | involves: 129P2/OlaHsd * C57BL/6 | J:191121 | View | ||||
ankyrin-B-related cardiac arrhythmia | Ank2em1Melr/Ank2em1Melr | B6.Cg-Ank2em1Melr | J:338515 | View | ||||
anterior segment dysgenesis | Pitx3ak/Pitx3ak | either: (involves: 129/Sv * C57BLKS) or (involves: 129/Sv * C57BL/6) | J:5084, J:82746, J:82907 | View | ||||
antithrombin III deficiency | Serpinc1tm1Dwr/Serpinc1tm1Dwr | involves: 129S1/Sv * 129X1/SvJ | J:115658 | 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 |
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 |
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 | 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 |
Aptxtm1Pmc/Aptxtm1Pmc Atmtm2.1Mfgc/Atmtm2.1Mfgc |
involves: 129 * C57BL/6 | J:316365 | View | ||||
ataxia telangiectasia | Atmtm1.1Mmpl/Atmtm1.1Mmpl | involves: 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J | J:226414 | View | ||||
ataxia telangiectasia | Atmtm1Awb/Atmtm1Awb | either: 129S6/SvEvTac-Atmtm1Awb or (involves: 129S6/SvEvTac * NIH Black Swiss) | J:34193, J:57115 | 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 | 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 | B6.Cg-Atmtm1Pmc | J:222034 | 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/Trf+ | BALB/cJ-Trfhpx | J:64456, J:8936 | View | ||||
atransferrinemia | Trfhpx/Trfhpx | 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 interstitial lung, joint, and kidney disease | Copatm1.1Shum/Copa+ | B6(CBA)-Copatm1.1Shum | J:288425 | 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/Atp6v1b2+ | involves: C57BL/6 | J:278514 | View | ||||
autosomal dominant congenital deafness with onychodystrophy | Atp6v1b2tm1Yoyu/Atp6v1b2tm1Yoyu | involves: C57BL/6 | J:278514 | View | ||||
autosomal dominant distal hereditary motor neuronopathy 2 | Hspb8tm1Vti/Hspb8tm1Vti | involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NCrl | J:284796 | View | ||||
autosomal dominant familial periodic fever | Tnfrsf1atm1Imx/Tnfrsf1atm1Imx | involves: 129S7/SvEvBrd * C57BL/6 | J:45147 | 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 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/Gna11+ | C57BL/6NCrl-Gna11em1Mman | J:280180 | View | ||||
autosomal dominant hypocalcemia 2 | Gna11em1Mman/Gna11em1Mman | 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 |
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 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 | Tectatm2Gpr/Tecta+ | involves: 129S/SvEv * C57BL/6J | J:101691 | 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 13 | Col11a2tm1Mne/Col11a2tm1Mne | FVB.129-Col11a2tm1Mne | J:71948 | View | ||||
autosomal dominant nonsyndromic deafness 22 | Myo6em1Bcgen/Myo6+ | involves: C57BL/6J * CBA/CaJ | J:288210 | View | ||||
autosomal dominant nonsyndromic deafness 22 | Myo6sv/Myo6sv | involves: B10.HA/(33NX)Sn * C57BL/6J | J:29898 | View | ||||
autosomal dominant nonsyndromic deafness 25 | Slc17a8tm1Selm/Slc17a8tm1Selm | involves: 129/Sv * C57BL/6 | J:139493 | 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 36 | Tmc1Mhdabth/Tmc1+ | C3HeB/FeJ-Tmc1Mhdabth/Ieg | J:86685 | 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 | Clcn7tm1.1Aros/Clcn7tm1.1Aros | involves: 129P2/OlaHsd * C57BL/6N | J:273179 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Mawa/Clcn7+ | involves: C57BL/6J * C57BL/6N * CD-1 | J:254787 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Mjec/Clcn7+ | involves: 129 * 129S/SvEv * C57BL/6 | J:203761 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Mjec/Clcn7+ | involves: 129S/SvEv * C57BL/6 * DBA/2J | J:203761 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Teti/Clcn7+ | involves: 129S2/SvPas * C57BL/6 | J:203761 | View | ||||
autosomal dominant osteopetrosis 2 | Clcn7tm1.1Teti/Clcn7tm1.1Teti | 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 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 | Col4a3tm1Dec/Col4a3tm1Dec | 129X1/SvJ-Col4a3tm1Dec | J:91619 | View | ||||
autosomal recessive Alport syndrome | Col4a3tm1Dec/Col4a3tm1Dec | involves: 129X1/SvJ * C57BL/6 | J:37963 | View | ||||
autosomal recessive Alport syndrome | Col4a3tm1Jhm/Col4a3tm1Jhm | involves: 129S1/Sv * 129X1/SvJ | J:37017, J:207595 | View | ||||
autosomal recessive Alport syndrome |
Col4a3tm1Jhm/Col4a3tm1Jhm Mmp9tm1Tvu/Mmp9tm1Tvu |
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ | J:63137 | View | ||||
autosomal recessive Alport syndrome | Col4a4bwk/Col4a4bwk | 129S1.NON(NZO)-Col4a4bwk/PgnJ | J:223185 | View | ||||
autosomal recessive Alport syndrome | Col4a4bwk/Col4a4bwk | D2.NON(NZO)-Col4a4bwk/GrsrJ | J:223185 | View | ||||
autosomal recessive Alport syndrome | Col4a4bwk/Col4a4bwk | NON;NZO-Col4a4bwk/J | J:223185 | View | ||||
autosomal recessive Alport syndrome | Col4a4m1Btlr/Col4a4m1Btlr | C57BL/6J-Col4a4m1Btlr | J:158794, J:170552 | View | ||||
autosomal recessive Alport syndrome | Col4a4m1H/Col4a4m1H | involves: C3H/HeH * C57BL/6J | J:285510 | 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 | Abca12el12/Abca12el12 | involves: 129/Sv * C57BL/6 | J:161652 | View | ||||
autosomal recessive congenital ichthyosis 4B | Abca12smsk/Abca12smsk | involves: C57BL/6J | J:262458 | View | ||||
autosomal recessive congenital ichthyosis 4B | Abca12tm1Lex/Abca12tm1Lex | involves: 129S/SvEvBrd * C57BL/6J | J:144062 | View | ||||
autosomal recessive congenital ichthyosis 4B | Abca12tm1Shzu/Abca12tm1Shzu | B6.129S-Abca12tm1Shzu | J:139048 | 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 distal hereditary motor neuronopathy 1 | Ighmbp2em1Cll/Ighmbp2em1Cll | FVB/NJ-Ighmbp2em1Cll | J:326540 | View | ||||
autosomal recessive distal hereditary motor neuronopathy 1 | Ighmbp2nmd-2J/Ighmbp2nmd-2J | B6.BKS-Ighmbp2nmd-2J/J | J:92862 | View | ||||
autosomal recessive intellectual developmental disorder 41 | Kptntm1a(EUCOMM)Wtsi/Kptntm1a(EUCOMM)Wtsi | C57BL/6N-Kptntm1a(EUCOMM)Wtsi | J:343200 | View | ||||
autosomal recessive isolated ectopia lentis 2 | Adamtsl4tvrm267/Adamtsl4tvrm267 | C57BL/6J-Adamtsl4tvrm267/Pjn | J:226844 | 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 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 2B | Dysfim/Dysfim | involves: SJL | J:57764 | 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 2C | Sgcgtm1Mcn/Sgcgtm1Mcn | involves: 129X1/SvJ * C57BL/6 | J:49871, J:57664, J:88456 | 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 2D | Sgcatm1Eeng/Sgcatm1Eeng | involves: 129S/SvEv * 129X1/SvJ | J:83034 | 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 | Sgcatm2Kcam/Sgcatm2Kcam | B6.129S6-Sgcatm2Kcam/J | J:250485 | 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 | Sgcdtm1Kcam/Sgcdtm1Kcam | involves: 129S1/Sv * 129X1/SvJ | J:57107 | 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 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+ |
involves: C57BL/6NCrlj * CBA/JNCrlj | J:207119 | 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 2J | Ttnmdm/Ttnmdm | Not Specified | J:74611 | 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 |
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 | Del(14Gjb6-Cryl1)1Lmon/Del(14Gjb6-Cryl1)1Lmon | C57BL/6JOlaHsd-Del(14Gjb6-Cryl1)1Lmon/Lmon | J:345081 | 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 |
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 1A | Gjb6tm1Kwi/Gjb6tm1Kwi | involves: 129P2/OlaHsd * C57BL/6 | J:80917 | View | ||||
autosomal recessive nonsyndromic deafness 2 | Myo7admbo2/Myo7admbo2 | involves: C57BL/6J | J:195666 | View | ||||
autosomal recessive nonsyndromic deafness 3 | Myo15ash2-2J/Myo15ash2-2J | involves: STOCK Rb(16.17)7Bnr | J:69998 | View | ||||
autosomal recessive nonsyndromic deafness 3 | Myo15atm1.1Jebd/Myo15atm1.1Jebd | involves: C57BL/6 * FVB/N | J:226820 | 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 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 9 | Otofdeaf5Jcs/Otofdeaf5Jcs | STOCK Otofdeaf5Jcs/Kjn | J:125960 | View | ||||
autosomal recessive nonsyndromic deafness 9 | Otoftm1Ugds/Otoftm1Ugds | involves: 129S2/SvPas * C57BL/6 | J:116097 | View | ||||
autosomal recessive nonsyndromic deafness 12 | Cdh2312J/Cdh2312J | involves: C57BL/6J | J:174758 | 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 16 | Strctm1Ugds/Strctm1Ugds | involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J | J:141421 | View | ||||
autosomal recessive nonsyndromic deafness 18A | Ush1cdfcr-2J/Ush1cdfcr-2J | B6;129S4 | J:85400 | View | ||||
autosomal recessive nonsyndromic deafness 18A | Ush1cdfcr-4J/Ush1cdfcr-4J | 129P3/J-Ush1cdfcr-4J/J | J:278662 | 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(KOMP)Wtsi/Ildr1tm1(KOMP)Wtsi | involves: C57BL/6N | J:217755, J:221592 | View | ||||
autosomal recessive nonsyndromic deafness 42 | Ildr1tm1.1Lwa/Ildr1tm1.1Lwa | involves: 129S6/SvEvTac * C57BL/6 | J:221594 | 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 | Marveld2tm1.1Sria/Marveld2tm1.1Sria | involves: 129X1/SvJ * C57BL/6J | J:201580 | View | ||||
autosomal recessive nonsyndromic deafness 49 | Marveld2tm1Sats/Marveld2tm1Sats | B6.Cg-Marveld2tm1Sats | J:261357 | 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 | S1pr2stdf/S1pr2stdf | involves: C57BL/6Brd * C57BL/6N | J:240361 | 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 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 | Tnfsf11gum/Tnfsf11gum | STOCK Tnfsf11gum/GrsrJ | J:223062 | View | ||||
autosomal recessive osteopetrosis 2 | Tnfsf11tles/Tnfsf11tles | involves: 129S6/SvEvTac * C57BL/6J | J:179743 | View | ||||
autosomal recessive osteopetrosis 2 | Tnfsf11tm1Ywc/Tnfsf11tm1Ywc | involves: 129P2/OlaHsd | J:233265 | 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 |
Ctsktm1(cre)Ska/Ctsk+ Plekhm1tm1.1Hzhao/Plekhm1tm1.1Hzhao |
involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj | J:236517 | View | ||||
autosomal recessive osteopetrosis 6 | Plekhm1tm1.2Hzhao/Plekhm1tm1.2Hzhao | involves: 129S1/Sv * C57BL/6J | 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 | Pkhd1tm1.1Ggg/Pkhd1tm1.1Ggg | involves: 129S/SvEv * 129S4/SvJae * C57BL/6 | J:125113 | View | ||||
autosomal recessive polycystic kidney disease | Pkhd1tm1Cjwa/Pkhd1tm1Cjwa | involves: 129S6/SvEvTac * FVB/N | J:140302 | 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 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 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 12 | Wwoxem1Mald/Wwoxem1Mald | FVB/N-Wwoxem1Mald | J:339564 | 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 | 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 | 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 | ||||
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 | Bbs1Gt1Nk/Bbs1Gt1Nk | involves: 129S7/SvEvBrd * C57BL/6J | J:92950 | 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 2 | Bbs2tm1.1Huss/Bbs2tm1.1Huss | involves: 129S6/SvEv * C57BL/6 | J:296033 | 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 3 | Arl6tm2Vcs/Arl6tm2Vcs | B6.129-Arl6tm2Vcs | J:257068 | View | ||||
Bardet-Biedl syndrome 4 | Bbs4Gt1Nk/Bbs4Gt1Nk | B6.129S7-Bbs4Gt1Nk | J:279506 | 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 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 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 | Lztfl1tm1.3Zpl/Lztfl1tm1.3Zpl | involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N | J:287261 | 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 | ||||
Barth syndrome | Gt(ROSA)26Sortm37(H1/tetO-RNAi:Tafazzin)Arte/? | Not Specified | J:176041 | View | ||||
Barth syndrome | Gt(ROSA)26Sortm37(H1/tetO-RNAi:Tafazzin)Arte/Gt(ROSA)26Sor+ | involves: 129S6/SvEvTac * C57BL/6J | J:167527 | View | ||||
Barth syndrome |
Tafazzinem1Xfa/Y Tg(myl7.L-cre)1118Tmhn/0 |
involves: C57BL/6NCrl * MF1 | J:339058 | View | ||||
Bartter disease type 1 | Slc12a1tm1Tkh/Slc12a1tm1Tkh | involves: 129S6/SvEvTac | J:62224 | View | ||||
Bartter disease type 1 | Slc12a1urehr3/Slc12a1urehr3 | involves: C3HeB/FeJ | J:159994 | View | ||||
Bartter disease type 2 | Kcnj1tm1Ges/Kcnj1tm1Ges | involves: 129X1/SvJ * Black Swiss | J:79354 | View | ||||
Bartter disease type 3 | Clcnkbem1Haca/Clcnkbem1Haca | C57BL/6-Clcnkbem1Haca | J:259681 | View | ||||
Bartter disease type 4a | Bsndtm1.1Suc/Bsndtm1.1Suc | involves: 129S4/SvJae * C57BL/6 | J:175265 | View | ||||
Bartter disease type 4a |
Bsndtm1Tjj/Bsndtm1Tjj Tg(Sox10-cre)1Wdr/0 |
involves: 129/Sv * 129X1/SvJ * C57BL/6 | J:143314 | 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 | Gp1bbtm1Ware/Gp1bb+ | Not Specified | J:93756 | View | ||||
Bernard-Soulier syndrome | Gp1bbtm1Ware/Gp1bbtm1Ware | Not Specified | J:93756 | View | ||||
Bernard-Soulier syndrome | Gp1bbtm2Frla/Gp1bbtm2Frla | involves: 129S2/SvPas * C57BL/6 | J:135065 | 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 |
Ahsptm1.1Mjwe/Ahsptm1.1Mjwe 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 |
Ahsptm1Mjwe/Ahsptm1Mjwe Hbb-b1tm1Unc/Hbb-b1+ Hbb-b2tm1Unc/Hbb-b2+ |
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 | J:94421 | View | ||||
beta thalassemia |
Hbatm1(HBA)Tow/Hbatm1(HBA)Tow Hbbtm2(HBG1,HBD,HBB*)Ryan/Hbbtm2(HBG1,HBD,HBB*)Ryan |
Not Specified | J:148521 | 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 | Hbb-b1MommeD7/Hbb-b1MommeD7 | involves: FVB/N | J:190446 | View | ||||
beta thalassemia | Hbb-b1Rbc13/Hbb-b1Rbc13 | involves: BALB/c * C57BL/6 | J:190446 | View | ||||
beta thalassemia |
Hbb-b1tm1Unc/Hbb-b1+ Hbb-b2tm1Unc/Hbb-b2+ |
B6;129-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 |
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-b1tm1Unc/Hbb-b1+ Hbb-b2tm1Unc/Hbb-b2+ Tg(HBB*)L2Pai/0 |
involves: 129P2/OlaHsd * C57BL/6 | J:97548 | View | ||||
beta thalassemia | Hbbd3th/Hbbd3th | involves: C57BL/6 * DBA/2J | J:7209 | View | ||||
beta thalassemia | Hbbtm1.1(HBG1,HBB*)Ryan/Hbb+ | involves: C57BL/6J | J:147906 | View | ||||
beta thalassemia | Hbbtm2Unc/Hbb+ | involves: 129P2/OlaHsd * C57BL/6J | J:64295 | View | ||||
BH4-deficient hyperphenylalaninemia A | Ptstm1Ich/Ptstm1Ich | involves: 129X1/SvJ * C57BL/6J | J:84764 | View | ||||
BH4-deficient hyperphenylalaninemia A | Ptstm1Thny/Ptstm1Thny | involves: 129/Sv * C57BL/6 | J:84533 | 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 |
Flcntm1Baba/Flcntm1.1Lss Tg(Cdh16-cre)91Igr/0 |
involves: C57BL/6 * FVB/N * ICR * SJL | J:130978 | View | ||||
Birt-Hogg-Dube syndrome |
Flcntm1Btt/Flcntm1Btt Tg(Cdh16-cre)91Igr/0 |
involves: 129S4/SvJaeSor * C57BL/6 * ICR | J:143922 | 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 | Blmtm1Ches/Blmtm1Ches | involves: 129S6/SvEvTac * NIH Black Swiss | J:50843 | View | ||||
Bloom syndrome | Blmtm1Ches/Blmtm3Brd | involves: 129S/SvEv * C57BL/6 * NIH Black Swiss | J:86827 | 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 | Blmtm1Grdn/Blm+ | involves: 129P2/OlaHsd * Black Swiss | J:79058 | View | ||||
Bloom syndrome | Blmtm3Brd/Blmtm3Brd | involves: 129S7/SvEvBrd * C57BL/6 | J:66261 | View | ||||
blue cone monochromacy | Opn1mwtm1a(EUCOMM)Wtsi/Opn1mwtm1a(EUCOMM)Wtsi | involves: C57BL/6J * C57BL/6N | J:249371 | View | ||||
Borjeson-Forssman-Lehmann syndrome | Phf6em1Azbi/Y | B6.Cg-Phf6em1Azbi | J:271089 | View | ||||
Borjeson-Forssman-Lehmann syndrome | Phf6tm1.2Avo/Y | involves: BALB/c * BALB/cJ * C57BL/6 * FVB/N | J:299742 | 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 | Eya1tm1Rilm/Eya1+ | either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * BALB/c) | J:57313 | View | ||||
branchiootorenal syndrome | Eya1tm1Rilm/Eya1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | 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 | Six1Cwe/Six1Cwe | C3HeB/FeJ-Six1Cwe | J:149467 | View | ||||
brittle cornea syndrome 1 | Zfp469em1Chms/Zfp469em1Chms | C57BL/6J-Zfp469em1Chms | J:311083 | View | ||||
Brugada syndrome 1 | Scn5atm1Agrc/Scn5a+ | involves: 129 | J:166438 | View | ||||
Brugada syndrome 1 | Scn5atm1Care/Scn5a+ | FVB.129P2-Scn5atm1Care/Care | J:128657 | View | ||||
Brugada syndrome 7 | Scn3btm1Clhh/Scn3btm1Clhh | 129S/SvEv-Scn3btm1Clhh | J:177262 | View | ||||
Brunner Syndrome | MaoaK284stop/Y | 129S6/SvEvTac-MaoaK284stop | J:136818 | View | ||||
Brunner Syndrome | MaoaTg(H2-K1-Ifnb1)8Seif/Y | involves: C3H/HeJ | J:26232 | 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 | ||||
buphthalmos | Cyp1b1tm1Gonz/Cyp1b1tm1Gonz | 129X1.Cg-Cyp1b1tm1Gonz | J:82280 | View | ||||
buphthalmos | Cyp1b1tm1Gonz/Cyp1b1tm1Gonz | B6.Cg-Cyp1b1tm1Gonz | J:82280 | View | ||||
buphthalmos | Cyp1b1tm1Gonz/Cyp1b1tm1Gonz | involves: 129X1/SvJ * C57BL/6J | J:82280 | View | ||||
buphthalmos |
Cyp1b1tm1Gonz/Cyp1b1tm1Gonz Tyrc-2J/Tyrc-2J |
B6.Cg-Tyrc-2J Cyp1b1tm1Gonz | J:82280 | 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 |
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 |
Notch1tm1Grid/Notch1+ Notch3tm1Grid/Notch3tm1Grid |
involves: 129S1/Sv * C57BL/6 | J:227333 | View | ||||
CADASIL 1 | Notch3hpbk/Notch3hpbk | C57BL/6J-Notch3hpbk/GrsrJ | J:222308 | View | ||||
CADASIL 1 | Notch3tm1.1Dwr/Notch3+ | involves: 129S/SvEv * Swiss | J:191454 | View | ||||
CADASIL 1 | Notch3tm1.1Dwr/Notch3tm1.1Dwr | involves: 129S/SvEv * Swiss | J:191454 | 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 | Sox9tm1.2Ksec/Sox9+ | involves: 129S/SvEv * C57BL/6 * FVB/N | J:332093 | View | ||||
campomelic dysplasia | Sox9tm1Crm/Sox9+ | involves: 129S7/SvEvBrd * C57BL/6 * CD-1 | J:69875 | 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 |
Sox9tm2Crm/Sox9+ Tg(Col2a1-cre)1Bhr/0 |
involves: 129S7/SvEvBrd * C57BL/6 * SJL | J:79879 | View | ||||
campomelic dysplasia |
Sox9tm2Crm/Sox9+ Tg(Prrx1-cre)1Cjt/0 |
involves: 129S7/SvEvBrd * C57BL/6J * SJL/J | J:79879 | View | ||||
campomelic dysplasia |
Sox9tm2Crm/Sox9tm2Crm 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 | ||||
Canavan disease | Aspadeaf14/Aspadeaf14 | BALB/c-Aspadeaf14 | J:211825 | View | ||||
Canavan disease | Aspanur7/Aspanur7 | involves: C57BL/6J | J:143201, J:226682 | View | ||||
Canavan disease | Aspanur7/Aspanur7 | STOCK Aspanur7/J | J:349783 | View | ||||
Canavan disease | Aspatm1a(EUCOMM)Wtsi/Aspatm1a(EUCOMM)Wtsi | involves: C57BL/6J * C57BL/6N | J:172582 | View | ||||
Canavan disease | Aspatm1Mata/Aspatm1Mata | involves: 129S5/SvEvBrd | J:89100, J:89099 | View | ||||
carbamoyl phosphate synthetase I deficiency disease | Cps1tm1Mw/Cps1tm1Mw | involves: 129S7/SvEvBrd * C57BL/6 | J:52334 | View | ||||
cardiofaciocutaneous syndrome | Braftm1Bbd/Braf+ | B6.129-Braftm1Bbd | J:170095 | View | ||||
cardiofaciocutaneous syndrome | Braftm1Bbd/Braf+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:170095 | View | ||||
cardiofaciocutaneous syndrome | Braftm1Bbd/Braf+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CD-1 | J:170095 | View | ||||
cardiofaciocutaneous syndrome |
Braftm1Tumg/Braf+ Tg(CAG-cre)2Osb/0 |
involves: C57BL * C57BL/6J * DBA | J:216228 | View | ||||
cardiofaciocutaneous syndrome |
Braftm1Tumg/Braf+ Tg(CAG-cre)2Osb/0 |
involves: C57BL * C57BL/6J * DBA * ICR | J:226977 | View | ||||
cardiofaciocutaneous syndrome |
Braftm1Wds/Braftm1Wds Raf1tm2Bacc/Raf1tm2Bacc H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129P2/OlaHsd * C57BL/6J * CBA/J | J:144862 | 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 |
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 | Prkar1atm1Gsm/Prkar1a+ | involves: 129X1/SvJ | J:93393 | View | ||||
cataract | Lim2Aca47/Lim2Aca47 | C57BL/6J-Lim2Aca47 | J:179533 | View | ||||
cataract | Lssem1Zhaol/Lssem1Zhaol | C57BL/6J-Lssem1Zhaol | J:316796 | View | ||||
cataract | Pank4em1Nju/Pank4em1Nju | Not Specified | J:301838 | View | ||||
cataract | Pax6132-14Neu/Pax6+ | involves: 101 * C3H | J:6686 | View | ||||
cataract | Trpm3em1Alsh/Trpm3em1Alsh | involves: C57BL/6J * CBA | J:307352 | View | ||||
cataract | Trpm3em1Alsh/Trpm3tm1Lex | involves: 129S5/SvEvBrd * C57BL/6J * CBA | J:307352 | View | ||||
cataract 1 multiple types | Gja8No2/Gja8+ | involves: 101 * C3H | J:49492 | View | ||||
cataract 1 multiple types | Gja8No2/Gja8No2 | involves: 101 * C3H | J:49492 | View | ||||
cataract 1 multiple types | Gja8R205G/Gja8R205G | B6.Cg-Gja8R205G | J:195727 | View | ||||
cataract 1 multiple types | Gja8tm1Paul/Gja8tm1Paul | involves: 129S4/SvJae * C57BL/6J | J:50894 | View | ||||
cataract 2 multiple types | CrygcChl3/Crygc+ | involves: 102/El * C3H/El | J:73804 | View | ||||
cataract 2 multiple types | CrygcChl3/CrygcChl3 | involves: 102/El * C3H/El | J:73804 | 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/Crygd+ | C3HeB/FeJ-CrygdAey4 | J:78154 | View | ||||
cataract 4 multiple types | CrygdAey4/CrygdAey4 | C3HeB/FeJ-CrygdAey4 | J:78154 | View | ||||
cataract 5 multiple types | Hsf4ldis1/Hsf4ldis1 | involves: C57BL/6 * CAST/EiJ * RIIIS/J | J:179658 | View | ||||
cataract 5 multiple types | Tg(Hsf4/EGFP)N7Spbh/0 | C57BL/6-Tg(Hsf4/EGFP)N7Spbh | J:230205 | 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/Cryaa+ | C3HeB/FeJ-CryaaAey7/Ieg | J:72928 | View | ||||
cataract 9 multiple types | CryaaAey7/CryaaAey7 | C3HeB/FeJ-CryaaAey7/Ieg | J:72928 | View | ||||
cataract 9 multiple types | Cryaalop18/Cryaalop18 | involves: CBA/CaGnLeJ | J:34933 | View | ||||
cataract 9 multiple types | Cryaatm1.1Ady/Cryaa+ | involves: 129 * C57BL/6 | J:132296 | View | ||||
cataract 9 multiple types | Cryaatm1.1Ady/Cryaatm1.1Ady | involves: 129 * C57BL/6 | J:132296 | View | ||||
cataract 9 multiple types | Cryaatm1Ady/Cryaa+ | involves: 129 | J:157274 | View | ||||
cataract 9 multiple types | Cryaatm1Ady/Cryaatm1Ady | involves: 129 | J:157274 | 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 10 multiple types | Cryba1Po1/Cryba1+ | C3HeB/FeJ-Cryba1Po1 | J:58912 | View | ||||
cataract 10 multiple types | Cryba1Po1/Cryba1Po1 | C3HeB/FeJ-Cryba1Po1 | J:58912 | View | ||||
cataract 14 multiple types | Gja3tm1.1Vmb/Gja3+ | involves: 129 * C57BL/6 | J:227244 | View | ||||
cataract 14 multiple types | Gja3tm1.1Vmb/Gja3tm1.1Vmb | involves: 129 * C57BL/6 | J:227244 | View | ||||
cataract 15 multiple types | MipCat-Fr/MipCat-Fr | involves: A/J | J:31574 | View | ||||
cataract 15 multiple types | MipCat-Lop/Mip+ | involves: STOCK Rb(6.15)1Ald | J:31574 | View | ||||
cataract 15 multiple types | MipCat-Tohm/MipCat-Tohm | involves: DDI | J:82971 | View | ||||
cataract 15 multiple types | MipCts/Mip+ | involves: C57BL/6J * CTS/Shi | J:196356 | View | ||||
cataract 15 multiple types | MipCts/MipCts | CTS/Shi | J:196356 | View | ||||
cataract 15 multiple types | MipHfi/Mip+ | involves: 101 * C3H | J:14285 | View | ||||
cataract 15 multiple types | MipHfi/MipHfi | involves: 101 * C3H | J:14285 | View | ||||
cataract 16 multiple types | Cryabtm1.1Ady/Cryabtm1.1Ady | involves: 129X1/SvJ * C57BL/6 | J:210399 | View | ||||
cataract 19 multiple types | Lim2To3/Lim2+ | involves: 102 * C3H/He * T STOCK | J:46338 | View | ||||
cataract 19 multiple types | Lim2To3/Lim2To3 | 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/Crygs+ | involves: 102 * C3H/He * T STOCK | J:34877, J:68109 | View | ||||
cataract 20 multiple types | CrygsOpj/CrygsOpj | 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 | CrygbClapper/Crygb+ | C57BL/6J-CrygbClapper | J:100851 | View | ||||
cataract 39 multiple types | CrygbClapper/CrygbClapper | C57BL/6J-CrygbClapper | J:100851 | View | ||||
cataract 39 multiple types | CrygbNop/Crygb+ | Not Specified | J:7589 | View | ||||
cataract 39 multiple types | CrygbNop/CrygbNop | Not Specified | J:7589 | View | ||||
cataract 39 multiple types | CrygbS11R/Crygb+ | A/J-CrygbS11R | J:132502 | View | ||||
cataract 39 multiple types | CrygbS11R/CrygbS11R | A/J-CrygbS11R | J:132502 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1.1Clhh/Ryr2tm1.1Clhh | 129S/SvEv-Ryr2tm1.1Clhh | J:186379 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1.1Maya/Ryr2+ | C57BL/6J-Ryr2tm1.1Maya | J:159451 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1Sgp/Ryr2+ | involves: 129/Sv * C57BL/6 | J:109683 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1Slh/Ryr2+ | involves: 129S7/SvEvBrd * C57BL/6 | J:111780 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1Slh/Ryr2+ | involves: 129S7/SvEvBrd * C57BL/6J | J:235432 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm2Amks/Ryr2+ | involves: 129S1/Sv * 129X1/SvJ | J:212640 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm2Hhv/Ryr2+ | involves: 129 * C57BL/6 | J:212870 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm3.1Amks/Ryr2+ | involves: C57BL/6 | J:212640 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm3.1Hhv/Ryr2+ | involves: 129S7/SvEvBrd * C57BL/6 | J:220671 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm4.1Amks/Ryr2+ | involves: 129 * C57BL/6 | J:212640 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 2 | Casq2tm1.1Sgp/Casq2tm1.1Sgp | involves: 129X1/SvJ * C57BL/6NCrL | J:151367 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 2 | Casq2tm1Jse/Casq2tm1Jse | involves: FVB/N | J:124211 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 2 | Casq2tm1Kpfe/Casq2tm1Kpfe | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:114621 | View | ||||
catecholaminergic polymorphic ventricular tachycardia 2 | Casq2tm2Jse/Casq2tm2Jse | Not Specified | J:124211 | 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 | Snap29tm1b(EUCOMM)Wtsi/Snap29tm1b(EUCOMM)Wtsi | involves: C57BL/6N * FVB/N | J:236759 | View | ||||
CEDNIK syndrome |
Snap29tm1c(EUCOMM)Wtsi/Snap29tm1c(EUCOMM)Wtsi Tg(KRT14-cre)1Cgn/0 |
involves: C57BL/6 * C57BL/6N * DBA/2 | J:236759 | View | ||||
central precocious puberty 2 | Mkrn3em1Rhu/Mkrn3+ | involves: C57BL/6 | J:305000 | View | ||||
cerebellar ataxia type 42 | Cacna1gem1Ftan/Cacna1g+ | C57BL/6NCrSlc-Cacna1gem1Ftan | J:278129 | View | ||||
cerebellar ataxia type 42 | Cacna1gem1Ftan/Cacna1gem1Ftan | C57BL/6NCrSlc-Cacna1gem1Ftan | J:278129 | 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-vmd/Atp8a2wl-vmd | C3H/HeSnJ-Atp8a2wl-vmd/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 | ||||
cerebellar ataxia, mental retardation and dysequlibrium syndrome | Car8wdl/Car8wdl | C57BLKS/J-Car8wdl/GrsrJ | J:230904 | View | ||||
cerebrocostomandibular syndrome |
E2f1Tg(Wnt1-cre)2Sor/E2f1+ Snrpbem1Lajm/Snrpb+ |
involves: C3H * C57BL/6 * C57BL/6J * CD1 | J:326544 | 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 axonal type 2S | Ighmbp2em1Cx/Ighmbp2em1Cx | C57BL/6J-Ighmbp2em1Cx/Cx | J:337488 | View | ||||
Charcot-Marie-Tooth disease axonal type 2S | Ighmbp2em5Cx/Ighmbp2em5Cx | C57BL/6J-Ighmbp2em5Cx/Cx | J:337488 | View | ||||
Charcot-Marie-Tooth disease axonal type 2Z | Morc2aem1Snupy/Morc2a+ | involves: C57BL/6 | J:341847 | View | ||||
Charcot-Marie-Tooth disease dominant intermediate C | Yars1tm1.1Rwb/Yars1tm1.1Rwb | 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-2J/Pmp22+ | C57BL/6J-Pmp22Tr-2J/GrsrJ | J:201866 | 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 | Pmp22Tr-J/Pmp22+ | involves: C57BL/6 | J:3394, J:98231 | View | ||||
Charcot-Marie-Tooth disease type 1A | Tg(Pmp22)247Ueli/0 | involves: C3H * C57BL/6 | J:98118 | 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-tTA)JY13Clh/0 Tg(tetO/CMV-Pmp22)JP18Clh/0 |
involves: C57BL/6J * CBA/Ca | J:69545 | 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 | Mpztm1Msch/Mpztm1Msch | involves: 129S7/SvEvBrd | J:42838 | View | ||||
Charcot-Marie-Tooth disease type 1B | Mpztm3.1Wra/Mpz+ | FVB.129S2(Cg)-Mpztm3.1Wra | J:241742 | 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 | 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 | 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 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(Mnx1-Mfn2*T105M,-EGFP)1Dcc/Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc | Not Specified | J:132035 | View | ||||
Charcot-Marie-Tooth disease type 2B | Rab7em2Rwb/Rab7+ | C57BL/6J-Rab7em2Rwb/RwbJ | J:346904 | View | ||||
Charcot-Marie-Tooth disease type 2B1 | Lmnatm1Stw/Lmnatm1Stw | involves: 129S1/Sv | J:75378 | View | ||||
Charcot-Marie-Tooth disease type 2D | Gars1C201R/Gars1+ | involves: BALB/cAnN * C3H/HeH * C57BL/6J | J:149830, J:179811 | View | ||||
Charcot-Marie-Tooth disease type 2D | Gars1em1Rwb/Gars1em2Rwb | involves: C57BL/6NJ * FVB/NJ | J:284948 | View | ||||
Charcot-Marie-Tooth disease type 2D | Gars1Nmf249/Gars1+ | C57BL/6J-Gars1Nmf249/J | J:112221 | View | ||||
Charcot-Marie-Tooth disease type 2D | Gars1Nmf249/Gars1+ | involves: C57BL/6J * CAST/Ei | J:179811 | View | ||||
Charcot-Marie-Tooth disease type 2E | Nefltm2.1Liem/Nefl+ | B6.Cg-Nefltm2.1Liem | J:220605 | View | ||||
Charcot-Marie-Tooth disease type 3 | Mpztm1Msch/Mpztm1Msch | involves: 129S7/SvEvBrd | J:42838 | View | ||||
Charcot-Marie-Tooth disease type 3 | Pmp22Tr-2J/Pmp22+ | C57BL/6J-Pmp22Tr-2J/GrsrJ | J:201866 | 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(RRF511)Byg/Sbf2Gt(RRF511)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:133391 | 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 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 | Ndrg1em1Lxli/Ndrg1em1Lxli | C57BL/6N-Ndrg1em1Lxli | J:330126 | 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 | Egr2tm1Jmi/Egr2tm1Jmi | Not Specified | J:96641 | View | ||||
Charcot-Marie-Tooth disease type 4E | Egr2tm2Jmi/Egr2tm2Jmi | B6.Cg-Egr2tm2Jmi | J:145949 | View | ||||
Charcot-Marie-Tooth disease type 4H | Fgd4tm1.1Ics/Fgd4tm1.1Ics | Not Specified | J:190437 | View | ||||
Charcot-Marie-Tooth disease type 4J | Fig4plt1/Fig4plt1 | involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL | J:122737 | 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 X-linked dominant 1 | Gjb1tm1Kwi/Gjb1tm1Kwi | involves: 129S4/SvJae | J:40955 | View | ||||
Charcot-Marie-Tooth disease X-linked dominant 1 | Gjb1tm1Kwi/Gjb1tm1Kwi | involves: 129S4/SvJae * C57BL/6 | J:36146 | View | ||||
Charcot-Marie-Tooth disease X-linked dominant 1 | Gjb1tm1Kwi/Y | involves: 129S4/SvJae | J:40955 | View | ||||
Charcot-Marie-Tooth disease X-linked dominant 1 | Gjb1tm1Kwi/Y | involves: 129S4/SvJae * C57BL/6 | J:36146 | View | ||||
Charlevoix-Saguenay spastic ataxia | Sacstm1(NCOM)Mfgc/Sacstm1(NCOM)Mfgc | Not Specified | J:182034 | View | ||||
Charlevoix-Saguenay spastic ataxia | Sacstm2Bebr/Sacstm2Bebr | involves: C57BL/6 | J:217753 | View | ||||
Chediak-Higashi syndrome | Lystbg-2Btlr/Lystbg-2Btlr | C57BL/6J-Lystbg-2Btlr | J:133617 | View | ||||
Chediak-Higashi syndrome | Lystbg-14J/Lystbg-14J | C3Fe;B6-Lystbg-14J | J:85200 | View | ||||
Chediak-Higashi syndrome | Lystbg-18J/Lystbg-18J | B6.Cg-Lystbg-18J/Boc | J:222308 | View | ||||
Chediak-Higashi syndrome | Lystbg-Btlr/Lystbg-Btlr | C57BL/6J-Lystbg-Btlr | J:133616 | View | ||||
Chediak-Higashi syndrome | Lystbg-grey/Lystbg-grey | C57BL/6-Lystbg-grey | J:106442 | 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 | ||||
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 | ||||
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 | ||||
Christianson syndrome | Slc9a6tm1Dgen/Slc9a6+ | B6.129P2-Slc9a6tm1Dgen/J | J:229166 | View | ||||
Christianson syndrome | Slc9a6tm1Dgen/Slc9a6tm1Dgen | B6.129P2-Slc9a6tm1Dgen/J | J:241124 | View | ||||
Christianson syndrome | Slc9a6tm1Dgen/Y | B6.129P2-Slc9a6tm1Dgen/J | J:241124, J:229166, J:262453 | View | ||||
CINCA Syndrome | Nlrp3tm3.1Hhf/Nlrp3+ | involves: 129 | J:202147 | View | ||||
cleidocranial dysplasia | Runx2tm1Jals/Runx2tm1Jals | involves: 129S7/SvEvBrd * C57BL/6 | J:143532 | View | ||||
cleidocranial dysplasia | Runx2tm1Kish/Runx2+ | involves: 129P2/OlaHsd * C57BL/6 | J:40783 | View | ||||
cleidocranial dysplasia | Runx2tm1Kish/Runx2tm1Kish | involves: 129P2/OlaHsd * C57BL/6 | J:40783, J:53069, J:54095 | View | ||||
cleidocranial dysplasia | Runx2tm1Mjo/Runx2+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:40784, J:53868 | View | ||||
Clouston syndrome | Gjb6tm2.2Kwi/Gjb6tm2.2Kwi | involves: 129P2/OlaHsd * BALB/c * C57BL/6 * CD-1 * SJL | J:208123 | View | ||||
Cockayne syndrome | Ercc6tm1Gvh/Ercc6tm1Gvh | B6J.129P2-Ercc6tm1Gvh | J:219993 | View | ||||
Cockayne syndrome | Ercc6tm1Gvh/Ercc6tm1Gvh | involves: 129P2/OlaHsd * FVB | J:40211 | View | ||||
Cockayne syndrome |
Ercc6tm1Gvh/Ercc6tm1Gvh Xpatm1Hvs/Xpatm1Hvs |
B6.129P2-Xpatm1Hvs Ercc6tm1Gvh | J:122013 | View | ||||
Cockayne syndrome |
Ercc6tm1Gvh/Ercc6tm1Gvh Xpatm1Hvs/Xpatm1Hvs |
involves: 129P2/OlaHsd * C57BL/6J | J:122013 | View | ||||
Cockayne syndrome | Ercc8tm1Jhjh/Ercc8tm1Jhjh | B6J.129P2-Ercc8tm1Jhjh | J:219993 | View | ||||
Cockayne syndrome | Ercc8tm1Jhjh/Ercc8tm1Jhjh | involves: 129P2/OlaHsd * C57BL/6J | J:74959 | View | ||||
Coffin-Lowry syndrome | Rps6ka3tm1.1Kry/Rps6ka3+ | involves: 129X1/SvJ | J:89403 | View | ||||
Coffin-Lowry syndrome | Rps6ka3tm1.1Kry/Rps6ka3tm1.1Kry | B6.129X1(Cg)-Rps6ka3tm1.1Kry | J:201540 | View | ||||
Coffin-Lowry syndrome | Rps6ka3tm1.1Kry/Rps6ka3tm1.1Kry | involves: 129X1/SvJ | J:89403 | View | ||||
Coffin-Lowry syndrome | Rps6ka3tm1.1Kry/Y | involves: 129X1/SvJ | J:89403, J:211945 | View | ||||
Coffin-Lowry syndrome | Rps6ka3tm1Ljg/Y | involves: 129 * C57BL/6 | J:67575, J:83536 | 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 | ||||
complex cortical dysplasia with other brain malformations 4 | Tubg1tm1.1Ics/Tubg1+ | involves: C57BL/6N | J:342743 | View | ||||
complex cortical dysplasia with other brain malformations 7 | Tubb2bbrdp/Tubb2bbrdp | involves: A/J * FVB | J:201099 | View | ||||
Compton-North congenital myopathy | Cntn1m1J/Cntn1m1J | B6;C-Cntn1m1J/GrsrJ | J:222308 | View | ||||
Compton-North congenital myopathy | Cntn1usl/Cntn1usl | B6.MRL-Cntn1usl/GrsrJ | J:222308 | View | ||||
Compton-North congenital myopathy | Cntn1usl/Cntn1usl | MRL/MpJ-Faslpr Cntn1usl/GrsrJ | J:222308 | View | ||||
cone-rod dystrophy | Dram2em1Jean/Dram2em1Jean | C57BL/6J-Dram2em1Jean | J:341125 | View | ||||
cone-rod dystrophy | Tlcd3bem1(IMPC)Bay/Tlcd3bem1(IMPC)Bay | C57BL/6NJ-Tlcd3bem1(IMPC)Bay/Mmnc | J:307901 | View | ||||
cone-rod dystrophy 2 | Crxem1Smgc/Crx+ | C57BL/6J-Crxem1Smgc | J:343281 | View | ||||
cone-rod dystrophy 2 | Crxrd23/Crxrd23 | B6.Cg-Crxrd23/BocJ | J:348234 | View | ||||
cone-rod dystrophy 3 | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae | J:141801 | View | ||||
cone-rod dystrophy 3 | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae * BALB/c | J:141801 | View | ||||
cone-rod dystrophy 6 | Gucy2etm1Gar/Gucy2etm1Gar | involves: 129S6/SvEvTac * C57BL/6 | J:77627 | View | ||||
cone-rod dystrophy 9 | Adam9tm1Bbl/Adam9tm1Bbl | involves: 129 | J:150865 | View | ||||
cone-rod dystrophy 16 | Cfap418em3Jyang/Cfap418em3Jyang | involves: C57BL/6 * CBA | J:259133 | View | ||||
cone-rod dystrophy 18 | Rab28tm1d(EUCOMM)Hmgu/Rab28tm1d(EUCOMM)Hmgu | involves: C57BL/6 * C57BL/6J * C57BL/6N | J:267522 | View | ||||
cone-rod dystrophy 18 | Rab28tm1d(EUCOMM)Wtsi/Rab28tm1d(EUCOMM)Wtsi | involves: C57BL/6 * C57BL/6J * C57BL/6N | J:267522 | View | ||||
congenital afibrinogenemia | Fggtm1Fjc/Fggtm1Fjc | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:75302 | 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 |
Phox2btm1Rth/Phox2b+ Hprt1tm1(CAG-cre)Mnn/? |
involves: 129 * 129S1/Sv * C57BL/6 | J:331513 | 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 | Bscl2tm1.1Lchan/Bscl2tm1.1Lchan | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:211142 | 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 | Bscl2tm1Geno/Bscl2tm1Geno | B6.129P2-Bscl2tm1Geno | J:200947 | 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-6J/Lama2dy-6J | involves: C57BL/6JEi * DBA/2J | J:56803 | 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 | Lama2dy-Pas/Lama2dy-Pas | involves: non-inbred stock | J:102806 | 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 | Lama2tm1Stk/Lama2tm1Stk | involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR | J:43145, J:167230 | 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 | Chattm1.1Jrs/Chattm1.1Jrs | Not Specified | J:91066 | View | ||||
congenital myasthenic syndrome 6 | Chattm1Fhg/Chattm1Fhg | involves: 129S2/SvPas * C57BL/6 | J:81738 | View | ||||
congenital myasthenic syndrome 8 | Agrnnmf380/Agrnnmf380 | C57BL/6J-Agrnnmf380/J | J:176117 | View | ||||
congenital myasthenic syndrome 9 | Musktm1.1Vwi/Musktm2Vwi | Not Specified | J:141024 | View | ||||
congenital myasthenic syndrome 9 |
Musktm1Vwi/Musktm1.1Vwi Tg(Ckmm-cre)5Khn/0 |
involves: C57BL/6J * FVB | J:106867 | View | ||||
congenital myasthenic syndrome 9 |
Musktm1Vwi/Musktm1Vwi Tg(Ckmm-cre)5Khn/0 |
involves: C57BL/6J * FVB | J:106867 | 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 myopathy 1A | Ryr1m1Nisw/Ryr1+ | 129S1.B6-Ryr1m1Nisw | J:219285 | View | ||||
congenital myopathy 1A | Ryr1tm1.1Dhm/Ryr1+ | involves: 129S2/SvPasCrl * 129S6/SvEvTac | J:155825 | View | ||||
congenital myopathy 1A | Ryr1tm1Tno/Ryr1tm1Tno | involves: 129S4/SvJae * C57BL/6J | J:18895 | 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 1A | Nyxnob/Nyxnob | BALB/c-Nyxnob | J:50824 | 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 1C | Trpm1nob11/Trpm1nob11 | B6.Cg-Trpm1nob11/BocJ | J:347037 | View | ||||
congenital stationary night blindness 1C | Trpm1rd15/Trpm1rd15 | B6.Cg-Trpm1rd15/BocJ | J:346902 | 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 2A | Cacna1fnob2/Cacna1fnob2 | AXB6/PgnJ | J:123811 | View | ||||
congenital stationary night blindness 2A | Cacna1fnob2/Y | AXB6/PgnJ | J:123811 | View | ||||
congenital stationary night blindness 2A | Cacna1fnob9/Cacna1fnob9 | B6(PWD)-Cacna1fnob9/BocJ | J:267160 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1.1Sdie/Cacna1f+ | involves: C57BL/6 | J:206214 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1.1Sdie/Cacna1ftm1.1Sdie | B6.Cg-Cacna1ftm1.1Sdie/J | J:212726 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1.1Sdie/Cacna1ftm1.1Sdie | involves: C57BL/6 | J:206214 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1.1Sdie/Y | B6.Cg-Cacna1ftm1.1Sdie/J | J:212726 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1.1Sdie/Y | involves: C57BL/6 | J:206214 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1.2Sdie/Cacna1ftm1.2Sdie | B6.Cg-Cacna1ftm1.2Sdie/J | J:212726 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1.2Sdie/Y | B6.Cg-Cacna1ftm1.2Sdie/J | J:212726 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1Ntbh/Cacna1ftm1Ntbh | B6.129-Cacna1ftm1Ntbh | J:102753 | View | ||||
congenital stationary night blindness 2A | Cacna1ftm1Ntbh/Y | B6.129-Cacna1ftm1Ntbh | J:102753 | 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 | Pde6batrd1/Pde6batrd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | 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 | Pde6batrd2/Pde6batrd2 | 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 | Pde6batrd3/Pde6batrd3 | 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 | 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 | Pde6brd1-2J/Pde6brd1-2J | C57BL/6J-Pde6brd1-2J/J | J:82238 | 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 | Pde6brd1-3H/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 | Pde6brd1-4H/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
congenital stationary night blindness autosomal dominant 2 | Pde6brd1/Pde6brd1 | Not Specified | J:24999 | View | ||||
Cornelia de Lange syndrome 1 | NipblGt(RRS564)Byg/Nipbl+ | involves: 129P2/OlaHsd * C57BL/6J * CD-1 | J:297059 | View | ||||
Cornelia de Lange syndrome 1 | NipblGt(RRS564)Byg/Nipbl+ | involves: 129P2/OlaHsd * CD-1 | J:154117 | View | ||||
Cornelia de Lange syndrome 3 | Smc3tm1.2Toshi/Smc3+ | B6.Cg-Smc3tm1.2Toshi | J:242006 | View | ||||
Cornelia de Lange syndrome 5 | Hdac8tm1.2Eno/Y | involves: 129S6/SvEvTac * C57BL/6J | J:297059 | View | ||||
cortical dysplasia-focal epilepsy syndrome | Cntnap2tm1Pele/Cntnap2tm1Pele | B6.129-Cntnap2tm1Pele | J:177110 | View | ||||
corticosteroid-binding globulin deficiency | Serpina6tm1.1Mmp/Serpina6tm1.1Mmp | involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL | J:164345, J:192931 | View | ||||
corticosteroid-binding globulin deficiency | Serpina6tm1Tew/Serpina6tm1Tew | involves: 129/SvEmcTer * C57BL/6N | J:112974 | View | ||||
cortisone reductase deficiency 2 | Hsd11b1tm1Yko/Hsd11b1tm1Yko | involves: 129P2/OlaHsd * MF1 | J:37960, J:45085, J:72402 | View | ||||
Costello syndrome |
Hrastm1Jaf/Hras+ Tg(CAG-cre)13Miya/0 |
involves: 129S6/SvEvTac * Black Swiss * C57BL/6 | J:204891 | View | ||||
Costello syndrome | Hrastm2Xbr/Hrastm2Xbr | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N | J:137729 | View | ||||
craniofrontonasal syndrome | Efnb1tm1.1Sor/Efnb1+ | involves: 129S4/SvJaeSor * C57BL/6 | J:115952 | View | ||||
craniotubular dysplasia Ikegawa type | Tmem53em1Ikeg/Tmem53em1Ikeg | Not Specified | J:306057 | View | ||||
cystathioninuria | Cthtm1Iish/Cthtm1Iish | B6.129-Cthtm1Iish/Iish | J:166184 | View | ||||
cystic fibrosis | Cftrem3Cwr/Cftrem3Cwr | C57BL/6J-Cftrem3Cwr/Cwr | J:262928 | View | ||||
cystic fibrosis | Cftrtm1.1Sdw/Cftrtm1.1Sdw | involves: C57BL/6 * C57BL/6J | J:323560 | 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 | Cftrtm1Eur/Cftrtm1Eur | B6.129P2-Cftrtm1Eur | J:189205 | View | ||||
cystic fibrosis | Cftrtm1Eur/Cftrtm1Eur | involves: 129P2/OlaHsd * FVB/N | J:28979 | View | ||||
cystic fibrosis | Cftrtm1Hgu/Cftrtm1Hgu | involves: 129P2/OlaHsd | J:24119 | 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 | Cftrtm1Kth/Cftrtm1Kth | B6.129S7-Cftrtm1Kth | J:112450 | View | ||||
cystic fibrosis | Cftrtm1Kth/Cftrtm1Kth | involves: 129S7/SvEvBrd * C57BL/6J | J:29074 | View | ||||
cystic fibrosis | Cftrtm1Unc/Cftrtm1Unc | B6.129P2-Cftrtm1Unc/J | J:58571, J:112450 | View | ||||
cystic fibrosis | Cftrtm1Unc/Cftrtm1Unc | involves: 129P2/OlaHsd | J:2079 | View | ||||
cystic fibrosis | Cftrtm2Cam/Cftrtm2Cam | involves: 129S/SvEv | J:27734 | View | ||||
cystic fibrosis | Cftrtm2Hgu/Cftrtm2Hgu | involves: 129P2/OlaHsd * C57BL/6 | J:74740 | View | ||||
cystic fibrosis | Cftrtm2Mrc/Cftrtm2Mrc | B6.129S6-Cftrtm2Mrc | J:112450 | View | ||||
cystic fibrosis | Cftrtm3Bay/Cftrtm3Bay | involves: 129S7/SvEvBrd | J:29656 | View | ||||
cystic fibrosis | Cftrtm3Hgu/Cftrtm3Hgu | involves: 129P2/OlaHsd | J:32766 | View | ||||
cystic fibrosis | Cftrtm3Mrc/Cftrtm3Mrc | B6.129S6-Cftrtm3Mrc | J:112450 | View | ||||
cystinosis | Ctnstm1Antc/Ctnstm1Antc | involves: 129/Sv * C57BL/6 | J:79610 | View | ||||
Danon disease | Lamp2tm1.2Ces/Y | involves: 129 * 129S4/SvJae * 129S6/SvEvTac * C57BL/6 * SJL | J:328713 | View | ||||
Danon disease | Lamp2tm1Psa/Lamp2tm1Psa | either: (involves: 129P2/OlaHsd * 129/Sv * C57BL/6J) or (involves: 129P2/OlaHsd * 129/Sv) | J:64151 | View | ||||
Danon disease | Lamp2tm1Psa/Lamp2tm1Psa | involves: 129P2/OlaHsd | J:253728 | View | ||||
Dent disease | Clcn5tm1Gug/Y | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:66560 | View | ||||
Dent disease | Clcn5tm1Tjj/Y | B6.129-Clcn5tm1Tjj | J:77111 | View | ||||
dentinogenesis imperfecta | Dspptm1Kul/Dspptm1Kul | involves: 129/Sv * C57BL/6 | J:84378 | View | ||||
Denys-Drash syndrome | Wt1tm1.1Lahe/Wt1+ | involves: 129S2/SvPas * C57BL/6 * FVB/NCrl * SJL | J:154995 | View | ||||
Denys-Drash syndrome | Wt1tm1Mlh/Wt1+ | 129P2/OlaHsd-Wt1tm1Mlh | J:135449 | 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 | Wt1tm1Vih/Wt1+ | involves: 129S7/SvEvBrd * C57BL/6 * MF1 | J:94225 | View | ||||
Denys-Drash syndrome | Wt1tm2Hst/Wt1+ | chimera involves: 129P2/OlaHsd * C57BL/6JLac * CBA/CaLac | J:53585, J:103489 | View | ||||
developmental and epileptic encephalopathy 2 | Cdkl5tm1.2Cogr/Cdkl5tm1.2Cogr | involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J | J:209635 | View | ||||
developmental and epileptic encephalopathy 2 | Cdkl5tm1.2Cogr/Y | involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J | J:209635 | View | ||||
developmental and epileptic encephalopathy 7 | Kcnq2tm1.1Lvi/Kcnq2+ | 129-Kcnq2tm1.1Lvi/Lvi | J:298666 | View | ||||
developmental and epileptic encephalopathy 14 | Kcnt1em1Lekk/Kcnt1+ | C57BL/6J-Kcnt1em1Lekk | J:287751 | View | ||||
developmental and epileptic encephalopathy 14 | Kcnt1em1Pqt/Kcnt1em1Pqt | C57BL/6J-Kcnt1em1Pqt | J:333512 | View | ||||
developmental and epileptic encephalopathy 16 | Tbc1d24em2Tbf/Tbc1d24em2Tbf | C57BL/6J-Tbc1d24em2Tbf | J:273646 | View | ||||
developmental and epileptic encephalopathy 17 | Gnao1em1Rneu/Gnao1+ | involves: C57BL/6J * C57BL/6NCrl | J:271137 | View | ||||
developmental and epileptic encephalopathy 17 | Gnao1tm2.1Rneu/Gnao1+ | B6.129S-Gnao1tm2.1Rneu | J:216850 | View | ||||
developmental and epileptic encephalopathy 17 | Gnao1tm2Rneu/Gnao1+ | B6.129S1-Gnao1tm2Rneu | J:271137 | View | ||||
developmental and epileptic encephalopathy 39 | Slc25a12Gt(OST123999)Lex/Slc25a12Gt(OST123999)Lex | involves: 129S5/SvEvBrd * C57BL/6 | J:243212 | View | ||||
developmental and epileptic encephalopathy 54 | Hnrnpuem1Frk/Hnrnpu+ | Not Specified | J:342579 | View | ||||
Diamond-Blackfan anemia 6 | Rpl5Skax23-Jus/Rpl5+ | 129S6.B6-Rpl5Skax23-Jus | J:330162 | 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 | Del(16Dgcr2-Hira)1Rak/+ | involves: 129/Sv * 129S6/SvEvTac * C57BL/6 * FVB/N * SJL | J:67796 | View | ||||
DiGeorge syndrome | Del(16Dgcr2-Hira)3Aam/+ | involves: 129S7/SvEvBrd | J:141432 | View | ||||
DiGeorge syndrome |
Kat6atm1Avo/Kat6a+ Tbx1tm1Bld/Tbx1+ |
involves: 129 * 129S7/SvEvBrd * BALB/c * C57BL/6 | J:188772 | View | ||||
DiGeorge syndrome |
Nkx2-5tm1(cre)Rjs/Nkx2-5+ Tbx1tm1Bld/Tbx1tm3Bld |
involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
DiGeorge syndrome | Tbx1tm1.1Dsr/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 | Tbx1tm1Bem/Tbx1+ | FVB.Cg-Tbx1tm1Bem | J:91664 | View | ||||
DiGeorge syndrome | Tbx1tm1Bem/Tbx1+ | involves: 129/Sv * C57BL/6J * SJL | J:67796 | View | ||||
DiGeorge syndrome | Tbx1tm1Bem/Tbx1tm1Bem | FVB.Cg-Tbx1tm1Bem | J:91664 | View | ||||
DiGeorge syndrome | Tbx1tm1Bld/Tbx1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:67409 | 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 | Tbx1tm1Dsr/Tbx1+ | either: 129/Sv or (involves: 129/Sv * C57BL/6) | J:93588 | View | ||||
DiGeorge syndrome | Tbx1tm1Dsr/Tbx1tm1Dsr | either: 129/Sv or (involves: 129/Sv * C57BL/6) | J:93588 | View | ||||
DiGeorge syndrome | Tbx1tm1Pa/Tbx1+ | involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ | J:70730 | View | ||||
DiGeorge syndrome | Tbx1tm1Pa/Tbx1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * Swiss Webster | J:70730 | 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 | Tbx1tm1Pa/Tbx1tm1Pa | involves: 129S1/Sv * 129X1/SvJ | J:94411 | 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 | Tbx1tm2Bld/Tbx1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
DiGeorge syndrome | Tbx1tm2Bld/Tbx1tm2Bld | involves: 129S7/SvEvBrd * C57BL/6 | J:91013 | View | ||||
dilated cardiomyopathy 1A | Lmnatm1Gbon/Lmnatm1Gbon | involves: 129S2/SvPas * C57BL/6 | J:187399 | View | ||||
dilated cardiomyopathy 1A | Lmnatm1Stw/Lmnatm1Stw | involves: 129S1/Sv | J:87613, J:131905 | View | ||||
dilated cardiomyopathy 1A | Lmnatm2.1Gbon/Lmna+ | involves: 129 * C57BL/6 | J:198526 | View | ||||
dilated cardiomyopathy 1A | Lmnatm3Stw/Lmnatm3Stw | involves: 129S1/Sv * 129S4/SvJaeSor * C57BL | J:100393 | 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 |
Ldb3tm4Chen/Ldb3tm4Chen Myl2tm1(cre)Krc/Myl2+ |
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * Black Swiss | J:144739 | View | ||||
dilated cardiomyopathy 1CC | Nexnem1Chen/Nexnem1Chen | C57BL/6J-Nexnem1Chen | J:301807 | View | ||||
dilated cardiomyopathy 1CC | Nexntm1.1Chen/Nexntm1.1Chen | Not Specified | J:290931 | View | ||||
dilated cardiomyopathy 1CC |
Nexntm1Chen/Nexntm1Chen Tg(myl7.L-cre)1118Tmhn/0 |
involves: MF1 | J:290931 | View | ||||
dilated cardiomyopathy 1CC |
Nexntm1Chen/Nexntm1Chen Tg(Tnnt2-cre)5Blh/0 |
involves: C57BL/6 * DBA/2 | J:290931 | View | ||||
dilated cardiomyopathy 1D | Tnnt2tm2.1Feah/Tnnt2+ | involves: 129S6/SvEvTac * FVB/N | J:243725 | View | ||||
dilated cardiomyopathy 1D | Tnnt2tm2Mmto/Tnnt2+ | involves: 129S/SvEv * C57BL/6 | J:137784 | View | ||||
dilated cardiomyopathy 1D | Tnnt2tm2Mmto/Tnnt2tm2Mmto | involves: 129S/SvEv * C57BL/6 | J:137784 | View | ||||
dilated cardiomyopathy 1DD | Rbm20em1Hide/Rbm20em1Hide | involves: C57BL/6J | J:297234 | View | ||||
dilated cardiomyopathy 1DD | Rbm20em3Wguo/Rbm20+ | C57BL/6-Rbm20em3Wguo | J:324088 | View | ||||
dilated cardiomyopathy 1DD | Rbm20em3Wguo/Rbm20em3Wguo | C57BL/6-Rbm20em3Wguo | J:324088 | View | ||||
dilated cardiomyopathy 1EE | Myh6tm2Ces/Myh6+ | involves: 129S/SvEv * 129X1/SvJ | J:114549 | View | ||||
dilated cardiomyopathy 1EE | Myh6tm2Ces/Myh6tm2Ces | involves: 129S/SvEv * 129X1/SvJ | J:114549 | View | ||||
dilated cardiomyopathy 1G | Ttntm1Brge/Ttn+ | B6.Cg-Ttntm1Brge | J:152736 | 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 1I | Destm1Cap/Destm1Cap | involves: 129S7/SvEvBrd * C57BL/6 | J:35123 | View | ||||
dilated cardiomyopathy 1L | Sgcdtm1Kcam/Sgcdtm1Kcam | involves: 129S1/Sv * 129X1/SvJ | J:57107 | View | ||||
dilated cardiomyopathy 1L | Sgcdtm1Mcn/Sgcdtm1Mcn | B6.129-Sgcdtm1Mcn/J | J:234761 | View | ||||
dilated cardiomyopathy 1L | Sgcdtm1Mcn/Sgcdtm1Mcn | involves: 129S1/Sv * 129T2/SvEmsJ * 129X1/SvJ | J:76730 | View | ||||
dilated cardiomyopathy 1L | Sgcdtm1Ojml/Sgcd+ | B6.129-Sgcdtm1Ojml | J:234761 | View | ||||
dilated cardiomyopathy 1M | Csrp3tm1Crni/Csrp3tm1Crni | Not Specified | J:38213 | View | ||||
dilated cardiomyopathy 1R | Tg(Myh6-Actc1*R312H)307Iko/? | involves: C57BL/6 | J:178587 | 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 | ||||
dilated cardiomyopathy 2F | Bag5em1Asay/Bag5em1Asay | C57BL/6JJcl-Bag5em1Asay | J:327046 | View | ||||
diphthamide deficiency syndrome 1 | Dph1em1Swei/Dph1em2Swei | C57BL/6J-Dph1em1Swei Dph1em2Swei | J:347602 | 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/Efemp1+ | involves: 129S6/SvEvTac * C57BL/6 * FVB/N | J:129901 | View | ||||
Doyne honeycomb retinal dystrophy | Efemp1tm1Eap/Efemp1tm1Eap | involves: 129S6/SvEvTac * C57BL/6 * FVB/N | J:129901 | View | ||||
Doyne honeycomb retinal dystrophy | Efemp1tm1Lmar/Efemp1+ | involves: 129X1/SvJ * BALB/c | J:129902 | View | ||||
Doyne honeycomb retinal dystrophy | Efemp1tm1Lmar/Efemp1tm1Lmar | involves: 129X1/SvJ * BALB/c | J:129902 | View | ||||
Dravet syndrome | Scn1atm1.1Kzy/Scn1a+ | involves: 129P2/OlaHsd * C3HeB/FeJ | J:260796 | 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 | Scn1atm1Wac/Scn1a+ | involves: 129S1/Sv * 129X1/SvJ * FVB/NJ | J:129998 | View | ||||
Dravet syndrome |
Scn1atm2.1Kzy/Scn1a+ Tg(Pvalb-cre)1Tama/0 |
involves: 129P2/OlaHsd * C57BL/6 * DBA | J:202863 | View | ||||
Dravet syndrome |
Scn1atm2.1Kzy/Scn1atm2.1Kzy Tg(Pvalb-cre)1Tama/0 |
involves: 129P2/OlaHsd * C57BL/6 * DBA | J:202863 | 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 | Sall4tm1Brd/Sall4+ | involves: 129S7/SvEvBrd * C57BL/6J | J:117866 | View | ||||
Duane-radial ray syndrome | Sall4tm1Ryn/Sall4+ | involves: 129P2/OlaHsd * C57BL/6J | J:118119 | View | ||||
Duchenne muscular dystrophy |
Barx2tm1Rsd/Barx2tm1Rsd Dmdmdx/Dmdmdx |
involves: 129 * C57BL/6 * C57BL/10ScSn | J:187799 | View | ||||
Duchenne muscular dystrophy |
Barx2tm1Rsd/Barx2tm1Rsd Dmdmdx/Y |
involves: 129 * C57BL/6 * C57BL/10ScSn | J:187799 | View | ||||
Duchenne muscular dystrophy | Dmdem1Eno/Y | involves: C57BL/6J | J:253191 | View | ||||
Duchenne muscular dystrophy | Dmdem4Eno/Dmdem4Eno | C57BL/6-Dmdem4Eno | J:285447 | View | ||||
Duchenne muscular dystrophy | Dmdem4Eno/Y | C57BL/6-Dmdem4Eno | J:285447 | View | ||||
Duchenne muscular dystrophy | Dmdem#Tve/Y | involves: C57BL/6 * CBA | J:275476 | View | ||||
Duchenne muscular dystrophy | DmdGt(ROSABetageo)1Mpd/Y | involves: 129S1/Sv | J:47968 | View | ||||
Duchenne muscular dystrophy | Dmdmdx-3Cv/Y | involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus | J:23375 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx-4Cv/Dmdmdx-4Cv Terctm1Rdp/Terctm1Rdp |
B6.Cg-Terctm1Rdp Dmdmdx-4Cv | J:200365 | View | ||||
Duchenne muscular dystrophy | Dmdmdx-5Cv/Dmdmdx-5Cv | B6Ros.Cg-Dmdmdx-5Cv/J | J:124861 | View | ||||
Duchenne muscular dystrophy | Dmdmdx-5Cv/Y | B6Ros.Cg-Dmdmdx-5Cv | J:177391 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/? Myod1tm1Jae/Myod1tm1Jae |
involves: 129S4/SvJae * C57BL/10ScSn | J:52248 | View | ||||
Duchenne muscular dystrophy | Dmdmdx/Dmdmdx | C57BL/10ScSn-Dmdmdx | J:150127 | View | ||||
Duchenne muscular dystrophy | Dmdmdx/Dmdmdx | C57BL/10ScSn-Dmdmdx/J | J:7361 | View | ||||
Duchenne muscular dystrophy | Dmdmdx/Dmdmdx | D2.B10-Dmdmdx | J:160773 | View | ||||
Duchenne muscular dystrophy | Dmdmdx/Dmdmdx | D2.B10-Dmdmdx/J | J:226314 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Dmdmdx Foxk1tm1Djg/Foxk1tm1Djg |
involves: 129S4/SvJae * C57BL/10ScSn | J:62225 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Dmdmdx Utrntm1Jrs/Utrntm1Jrs |
involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn | J:42389, J:59675 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Dmdmdx Utrntm1Ked/Utrntm1Ked |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA | J:42388 | View | ||||
Duchenne muscular dystrophy | Dmdmdx/Y | C57BL/10ScSn-Dmdmdx | J:150127, J:177391 | View | ||||
Duchenne muscular dystrophy | Dmdmdx/Y | C57BL/10ScSn-Dmdmdx/J | J:7361 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Y Dtnatm1Jrs/Dtnatm1Jrs |
involves: 129X1/SvJ * C57BL/10ScSn | J:59675 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Y Dtnatm1Jrs/Dtnatm1Jrs Utrntm1Jrs/Utrntm1Jrs |
involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn | J:59675 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Y Foxk1tm1Djg/Foxk1tm1Djg |
involves: 129S4/SvJae * C57BL/10ScSn | J:62225 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Y Terctm1Rdp/Terctm1Rdp |
involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL | J:167294 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Y Tg(DMD*)#Spc/0 |
involves: 129P2/OlaHsd * C57BL/10ScSn * DBA/2 | J:280218 | View | ||||
Duchenne muscular dystrophy |
Dmdmdx/Y Utrntm1Jrs/Utrn+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn | J:140282 | View | ||||
Duchenne muscular dystrophy | Dmdtm1.1Khan/Y | involves: C57BL/6 * CBA | J:96210 | View | ||||
Duchenne muscular dystrophy | Dmdtm1Kmf/Y | involves: C57BL/6 | J:233298 | View | ||||
Duchenne muscular dystrophy | Dmdtm1Mok/Y | involves: 129S/SvEv | J:43164 | 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 | Trp63tm1Brd/Trp63tm1Brd | involves: 129S7/SvEvBrd * C57BL/6J | J:54636 | 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 | Trp63tm2Brd/Trp63tm2Brd | involves: 129S7/SvEvBrd * C57BL/6J | J:54636 | View | ||||
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 3 | Trp63tm3Aam/Trp63+ | involves: 129S7/SvEvBrd | J:294158 | 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 | Evc2tm1.1Mis/Evc2tm1.1Mis | involves: 129X1/SvJ * C57BL/6 | J:226455 | View | ||||
Ellis-Van Creveld syndrome | Evctm1Jago/Evctm1Jago | involves: 129S7/SvEvBrd * C57BL/6 | J:124105 | View | ||||
endocrine-cerebro-osteodysplasia syndrome | Cilk1tm1.1Zfu/Cilk1tm1.1Zfu | B6.Cg-Cilk1tm1.1Zfu/Zfu | 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 | 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 Ogna type | Plectm7.1Gwi/Plec+ | involves: 129P2/OlaHsd * C57BL/6 | J:179812 | View | ||||
epidermolysis bullosa simplex Ogna type | Plectm7.1Gwi/Plectm7.1Gwi | involves: 129P2/OlaHsd * C57BL/6 | J:179812 | 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/Prrt2+ | B6(Cg)-Prrt2tm1d(KOMP)Wtsi | J:299667 | View | ||||
episodic kinesigenic dyskinesia 1 | Prrt2tm1d(KOMP)Wtsi/Prrt2tm1d(KOMP)Wtsi | B6(Cg)-Prrt2tm1d(KOMP)Wtsi | J:299667 | View | ||||
erythrokeratodermia variabilis | Gjb3tm2.1Kwi/Gjb3+ | involves: 129P2/OlaHsd * C57BL/6 | J:121802 | View | ||||
factor VIII deficiency | F8tm1Kaz/Y | involves: 129S4/SvJae * C57BL/6 | J:24941 | View | ||||
factor VIII deficiency | F8tm2Kaz/Y | involves: 129S4/SvJae * C57BL/6 | J:24941 | 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 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 hyperinsulinemic hypoglycemia 3 |
Gcktm1Ydor/Gck+ Tg(Ins2-cre)25Mgn/0 |
involves: C57BL/6 * C57BL/6J * DBA | J:302600 | 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 | Lpltm1Bres/Lpl+ | involves: 129S4/SvJae * C57BL/6J | J:30062 | View | ||||
familial lipoprotein lipase deficiency | Lpltm1Bres/Lpltm1Bres | involves: 129S4/SvJae * C57BL/6J | J:30062 | View | ||||
familial lipoprotein lipase deficiency | Lpltm1Sem/Lpl+ | involves: 129P2/OlaHsd * C57BL/6J | J:25652 | View | ||||
familial lipoprotein lipase deficiency | Lpltm1Sem/Lpltm1Sem | involves: 129P2/OlaHsd * C57BL/6J | J:25652 | View | ||||
familial Mediterranean fever | Mefvtm1Chae/Mefvtm1Chae | either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6) | J:82763 | 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 temporal lobe epilepsy 1 | Lgi1tm1.1Ics/Lgi1tm1.1Ics | involves: 129S2/SvPas * BALB/c * C57BL/6 | J:182795 | 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 | 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 | Fancatm1.1Wong/Fancatm1.1Wong | involves: C57BL/6 | J:85108 | 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 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 |
Aldh2tm1a(EUCOMM)Wtsi/Aldh2tm1a(EUCOMM)Wtsi Fancd2tm1Hou/Fancd2tm1Hou |
involves: 129S4/SvJae * C57BL/6J * C57BL/6N | J:193232 | View | ||||
Fanconi anemia complementation group D2 | Fancd2em1Tzh/Fancd2em1Tzh | C57BL/6-Fancd2em1Tzh | J:284566 | View | ||||
Fanconi anemia complementation group D2 |
Fancd2Gt(OST57859)Lex/Fancd2Gt(OST57859)Lex Usp1tm1.1Ada/Usp1tm1.1Ada |
involves: 129S5/SvEvBrd * C57BL/6 | J:146616 | 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 | Fancd2tm1Hou/Fancd2tm1Hou | involves: 129S4/SvJae * C57BL/6J | J:84892 | 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 |
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 |
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 |
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 dermal hypoplasia |
Porcntm1.1Lcm/Porcn+ Edil3Tg(Sox2-cre)1Amc/Edil3+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:173672 | View | ||||
focal dermal hypoplasia | Porcntm1.1Lcm/Porcntm1.2Lcm | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 | J:218165 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Lcm/Porcntm1.2Lcm Tg(Six3-cre)69Frty/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2 | J:218165 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Lcm/Y H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1 | J:218165 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Lcm/Y H2az2Tg(Wnt1-cre)11Rth/H2az2+ Tg(rx3-icre)1Mjam/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J * CD-1 | J:218165 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Lcm/Y Tg(rx3-icre)1Mjam/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 | J:218165 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Vdv/Porcn+ Hprt1tm1(CAG-cre)Mnn/Hprt1+ |
involves: 129S/Sv * C57BL/6J | J:186934 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Vdv/Porcn+ Tg(EIIa-cre)C5379Lmgd/0 |
involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N | J:186934 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Vdv/Y Tg(EIIa-cre)C5379Lmgd/0 |
involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J * FVB/N | J:186934 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Vdv/Y Tg(KRT14-cre)1Efu/0 |
involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6J | J:186934 | View | ||||
focal dermal hypoplasia |
Porcntm1.1Vdv/Y Tg(Prrx1-cre)1Cjt/0 |
involves: 129S4/SvJaeSor * 129S5/SvEvBrd * C57BL/6 * SJL/J | J:186934 | View | ||||
focal dermal hypoplasia | Porcntm1.2Lcm/Porcntm1.2Lcm | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 * DBA/2 | J:218165 | View | ||||
focal dermal hypoplasia | Porcntm1Vdv/Porcn+ | chimera involves: 129S5/SvEvBrd * C57BL/6J | J:186934 | View | ||||
focal dermal hypoplasia | Porcntm1Vdv/Y | chimera involves: 129S5/SvEvBrd * C57BL/6J | J:186934 | View | ||||
focal segmental glomerulosclerosis 1 | Actn4tm1Mrpk/Actn4tm1Mrpk | 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*E896K)F75aWalz/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 3 | Cd2apem1Irgu/Cd2apem1Irgu | C57BL/6-Cd2apem1Irgu | J:294238 | View | ||||
foveal hypoplasia 2 | Slc38a8em1Lmon/Slc38a8em1Lmon | B6.Cg-Slc38a8em1Lmon | J:343795 | View | ||||
fragile X syndrome |
Fmr1tm1.1Cidz/Fmr1tm1.1Cidz Tg(Pcp2-cre)2Mpin/0 |
involves: 129S1/Sv * 129X1/SvJ | J:101021 | View | ||||
fragile X syndrome | Fmr1tm1.1Ics/Fmr1tm1.1Ics | C57BL/6-Fmr1tm1.1Ics | J:304982 | View | ||||
fragile X syndrome | Fmr1tm1.2Cidz/Y | involves: 129P2/OlaHsd * 129/Sv * C57BL/6 * FVB/N | J:176553 | View | ||||
fragile X syndrome | Fmr1tm1Cgr/Fmr1tm1Cgr | involves: 129P2/OlaHsd | J:101021 | View | ||||
fragile X syndrome | Fmr1tm1Cgr/Fmr1tm1Cgr | involves: 129P2/OlaHsd * C57BL/6J | J:19220 | View | ||||
fragile X syndrome | Fmr1tm1Cgr/Y | involves: 129P2/OlaHsd | J:34449, J:101021 | View | ||||
fragile X syndrome | Fmr1tm1Cgr/Y | involves: 129P2/OlaHsd * C57BL/6J | J:19220, J:221083 | View | ||||
fragile X syndrome | Fmr1tm1Rbd/Y | B6.129-Fmr1tm1Rbd | J:155593 | View | ||||
fragile X syndrome | Fmr1tm1Usdn/Fmr1tm1Usdn | B6.129S6(Cg)-Fmr1tm1Usdn | J:196840 | View | ||||
fragile X syndrome | Fmr1tm1Usdn/Y | involves: 129S6/SvEvTac * C57BL/6 | J:170720 | View | ||||
fragile X-associated tremor/ataxia syndrome | Fmr1tm2Cgr/Y | involves: 129P2/OlaHsd * C57BL/6J * FVB | J:104445 | View | ||||
Friedreich ataxia | Fxnem8Lutzy/Fxnem8Lutzy | C57BL/6J-Fxnem8Lutzy | J:299300 | View | ||||
Friedreich ataxia | Fxntm1.1Pand/Fxntm1Mkn | B6.Cg-Fxntm1.1Pand Fxntm1Mkn/J | J:242978 | 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 | ||||
Friedreich ataxia | Fxntm1Mkn/Fxntm1Pand | involves: 129/Sv * C57BL/6 | J:216422 | 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 | Gt(ROSA)26Sortm1(H1/tetO-RNAi:Fxn)Dhg/Gt(ROSA)26Sor+ | B6.129-Gt(ROSA)26Sortm1(H1/tetO-RNAi:Fxn)Dhg | J:254962 | 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 |
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 | ||||
Fukuyama congenital muscular dystrophy | Fktntm1Ttd/Fktntm1Ttd | involves: 129S7/SvEvBrd * C57BL/6 | J:97950 | View | ||||
Fukuyama congenital muscular dystrophy | Fktntm1Ttd/Fktntm2(FCMD)Ttd | involves: 129S7/SvEvBrd | J:144746 | View | ||||
GAND syndrome | Gatad2btm1a(EUCOMM)Hmgu/Gatad2b+ | C57BL/6N-Gatad2btm1a(EUCOMM)Hmgu | J:344365 | 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 | Slc12a3em3Gpt/Slc12a3em4Gpt | involves: C57BL/6 | J:336073 | 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 Ia | G6pc1em1Jyc/G6pc1em1Jyc | involves: 129S4/SvJae * C57BL/6 | J:320697 | View | ||||
glycogen storage disease Ia |
G6pc1tm1.1Ics/G6pc1tm1.1Ics Albtm1(cre/ERT2)Mtz/Alb+ |
involves: 129S2/SvPas * C57BL/6J | J:195257 | View | ||||
glycogen storage disease Ia |
G6pc1tm1.1Ics/G6pc1tm1.1Ics Tg(Kap-icre)29066/2Sig/0 |
involves: 129S2/SvPas * C57BL/6J * SJL | J:238264 | View | ||||
glycogen storage disease Ia | G6pc1tm1Jyc/G6pc1tm1Jyc | involves: 129S4/SvJae | J:33212 | View | ||||
glycogen storage disease Ia | G6pc1tm2.2Jyc/G6pc1tm2.2Jyc | involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J * FVB/N | J:155990 | View | ||||
glycogen storage disease II | Gaatm1.1Rabn/Gaatm1.1Rabn | involves: 129X1/SvJ * C57BL/6 * FVB/N | J:76435 | View | ||||
glycogen storage disease II | Gaatm1Rabn/Gaatm1Rabn | involves: 129X1/SvJ * C57BL/6 | J:48839, J:76435 | View | ||||
glycogen storage disease II |
Gaatm1Rabn/Gaatm1Rabn Tg(CMV-GAA*P545L)#Kjv/0 |
involves: 129X1/SvJ * C57BL/6 | J:219022 | View | ||||
glycogen storage disease II | Gaatm1Vdp/Gaatm1Vdp | either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB) | J:45386 | View | ||||
glycogen storage disease II | Gaatm2Rabn/Gaatm2Rabn | involves: 129X1/SvJ * C57BL/6 | J:76435 | View | ||||
glycogen storage disease III | Agltm1a(EUCOMM)Wtsi/Agltm1a(EUCOMM)Wtsi | involves: C57BL/6N | J:212003 | View | ||||
glycogen storage disease III | Agltm1Geno/Agltm1Geno | C57BL/6J-Agltm1Geno | J:218471 | View | ||||
glycogen storage disease IV | Gbe1m1Yty/Gbe1m1Yty | C3HeB/FeJ-Gbe1m1Yty | J:167233 | View | ||||
glycogen storage disease IV | Gbe1tm1.1Hoa/Gbe1tm1.1Hoa | involves: 129S7/SvEvBrd | J:176889 | View | ||||
glycogen storage disease IV | Gbe1tm1Hoa/Gbe1tm1Hoa | involves: 129S7/SvEvBrd | J:176889 | View | ||||
glycogen storage disease IV | Gbe1tm2.1Hoa/Gbe1tm2.1Hoa | involves: 129S7/SvEvBrd | J:226481 | View | ||||
glycogen storage disease IXd | Phka1I/FnLn/Phka1I/FnLn | I/FnLn | J:42850 | View | ||||
glycogen storage disease IXd | Phka1I/FnLn/Y | I/FnLn | J:42850 | View | ||||
glycogen storage disease V | Pygmtm1.1Adru/Pygmtm1.1Adru | involves: 129 * C57BL/6J | J:226312 | View | ||||
glycogen storage disease VI | Pygltm1a(KOMP)Wtsi/Pygltm1a(KOMP)Wtsi | C57BL/6N-Pygltm1a(KOMP)Wtsi | J:284765 | View | ||||
glycogen storage disease VII | Pfkmtm1Fbos/Pfkmtm1Fbos | involves: 129S6/SvEvTac * C57BL/6J | J:152153 | View | ||||
glycogen storage disease XV | Gyg1tm1a(KOMP)Wtsi/Gyg1tm1a(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 | ||||
gnathodiaphyseal dysplasia | Ano5em2Huyi/Ano5em2Huyi | C57BL/6-Ano5em2Huyi | J:336715 | 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-l34J/Myo5ad-l34J | BALB/cJ-Myo5ad-l34J/GrsrJ | J:216055 | View | ||||
Griscelli syndrome type 1 | Myo5ad-n/Myo5ad-n | B10.D2-H2d/nSnJ | J:171603 | 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 | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Grntm2.1Far/Grntm2.1Far | involves: 129S4/SvJae * C57BL/6 | J:259651 | 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 |
Notch2tm2.1Ecan/Notch2tm2.1Ecan Tg(BGLAP-cre)1Clem/0 |
involves: C57BL/6J * FVB/NJ | J:246017 | View | ||||
Hajdu-Cheney syndrome | Notch2tm2.2Ecan/Notch2+ | involves: 129S1/Sv * C57BL/6J | J:246017 | View | ||||
hand-foot-genital syndrome | Hoxa13Hd/Hoxa13+ | B6C3Fe-a/a Hoxa13Hd Mcoln3Va-J/J | J:54823 | View | ||||
hand-foot-genital syndrome | Hoxa13Hd/Hoxa13Hd | B6C3Fe-a/a Hoxa13Hd Mcoln3Va-J/J | J:58731 | View | ||||
hand-foot-genital syndrome | Hoxa13Hd/Hoxa13Hd | involves: MYA/Hu | J:64253, J:5211 | View | ||||
hand-foot-genital syndrome | Hoxa13tm1Jwi/Hoxa13+ | involves: 129S7/SvEvBrd | J:94412 | View | ||||
hand-foot-genital syndrome | Hoxa13tm1Jwi/Hoxa13tm1Jwi | involves: 129S7/SvEvBrd | J:94412 | View | ||||
hemophilia B | F9em1Dlli/Y | involves: C57BL/6J | J:262204 | View | ||||
hemophilia B | F9em3Dlli/Y | involves: C57BL/6J | J:262204 | View | ||||
hemophilia B | F9tm1Dws/Y | involves: 129P2/OlaHsd * C57BL/6 | J:44497 | View | ||||
hemophilia B | F9tm1Emg/Y | involves: 129S/SvEv * C57BL/6J | J:48501 | View | ||||
hemophilia B | F9tm1Ver/F9tm1Ver | involves: 129/Sv * C57BL/6 | J:43590 | View | ||||
hereditary hemorrhagic telangiectasia | Acvrl1tm1Enl/Acvrl1+ | involves: C57BL/6 | J:82115 | 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 |
Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Tg(Acvrl1-cre)L1Spo/0 |
involves: 129 * FVB | J:154620 | View | ||||
hereditary hemorrhagic telangiectasia |
Acvrl1tm2.1Spo/Acvrl1tm2.1Spo Tg(Tal1-cre/ERT)1Jrg/0 |
involves: 129 * C57BL/6 | J:227170 | 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 | Engtm1Dyl/Engtm1Dyl | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:55403 | 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 | Engtm1Mle/Eng+ | involves: 129P2/OlaHsd * C57BL/6 | J:58502 | 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 |
Engtm2.1Hma/Engtm2.1Hma Tg(Tagln-cre)1Her/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:212952 | 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 |
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 |
Ext1tm1Vcs/Ext1tm1Vcs Tg(Col2a1-rtTA,tetO-cre)22Pjro/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:157599 | 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 | Pmp22tm1Lnot/Pmp22+ | Not Specified | J:104989 | View | ||||
hereditary neuropathy with liability to pressure palsies | Pmp22tm1Ueli/Pmp22tm1Ueli | involves: 129S/SvEv | J:29517 | View | ||||
hereditary neuropathy with liability to pressure palsies | Pmp22Tr-2J/Pmp22+ | C57BL/6J-Pmp22Tr-2J/GrsrJ | J:201866 | 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 2 |
Plp1tm1c(EUCOMM)Wtsi/Y Cnptm1(cre)Kan/Cnp+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N | J:245100 | View | ||||
hereditary spastic paraplegia 2 | Plp1tm1Kan/Y | involves: 129S1/Sv * 129X1/SvJ | J:48031, J:245100 | 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 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-2J/Kif1algdg-2J | C57BL/6J-Kif1algdg-2J/CxJ | J:229662 | View | ||||
hereditary spastic paraplegia 30 | Kif1algdg/Kif1algdg | C3.Cg-Kif1algdg/GrsrJ | 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 spastic paraplegia 80 | Ubap1em1Yta/Ubap1+ | involves: C57BL/6 * C57BL/6N * DBA/2 | J:332139 | View | ||||
hereditary spherocytosis type 1 | Ank1M1Wlst/Ank1M1Wlst | involves: 129S1/SvImJ * C3H/HeJ * C57BL/6 | J:170562 | 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 | Ank1pale/Ank1pale | C57BL/6J-Ank1pale/GrsrJ | J:222308 | View | ||||
hereditary spherocytosis type 1 | Ank1Rbc2/Ank1Rbc2 | involves: 129S1/Sv * BALB/c | J:148127 | 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 3 | Spta1sph-ha/Spta1sph-ha | involves: DBA/1J | J:14946, J:30699 | 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 | ||||
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 |
Ap3b1pe/Ap3b1pe Hps1ep/Hps1ep |
involves: C3H/He * C3HeB/FeJ * C57BL/6J | J:85431 | View | ||||
Hermansky-Pudlak syndrome 1 | Hps1ep-7J/Hps1ep-7J | CAST/EiJ-Hps1ep-7J/GrsrJ | J:198843 | View | ||||
Hermansky-Pudlak syndrome 1 | Hps1ep/Hps1ep | B6.C3Fe-Hps1ep/J | J:80751 | View | ||||
Hermansky-Pudlak syndrome 1 | Hps1ep/Hps1ep | involves: C3HeB/FeJ * C57BL/6J | J:7416 | View | ||||
Hermansky-Pudlak syndrome 2 | Ap3b1pe-rim2/Ap3b1pe-rim2 | involves: B10.A(R201) * C57BL/10Slc | J:42685 | View | ||||
Hermansky-Pudlak syndrome 2 | Ap3b1pe/Ap3b1pe | B6.C3-Ap3b1pe/J | J:221384 | 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-hz/Hps5ru2-hz | involves: DBA/2J | J:81444 | 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 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 | ||||
high myopia-sensorineural deafness syndrome | Slitrk6tm1.1Jaru/Slitrk6tm1.1Jaru | B6.129P2-Slitrk6tm1.1Jaru | J:201352 | View | ||||
HMG-CoA synthase 2 deficiency | Hmgcs2em1(IMPC)Tcp/Hmgcs2+ | C57BL/6NCrl-Hmgcs2em1(IMPC)Tcp | J:326918 | View | ||||
HMG-CoA synthase 2 deficiency | Hmgcs2em1(IMPC)Tcp/Hmgcs2em1(IMPC)Tcp | C57BL/6NCrl-Hmgcs2em1(IMPC)Tcp | J:326918 | 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 |
Disp1icb/Disp1tm1Amc Shhtm1Amc/Shh+ |
involves: 129X1/SvJ * C57BL/6J | J:92058 | View | ||||
holoprosencephaly 3 | Shhtm1Chg/Shhtm1Chg | involves: 129S1/Sv * 129X1/SvJ | J:35802 | 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/Boc+ Cdontm1Rsk/Cdontm1Rsk |
involves: 129/Sv * 129S6/SvEvTac | J:171767 | View | ||||
holoprosencephaly 11 |
Boctm1Rsk/Boctm1Rsk Cdontm1Rsk/Cdontm1Rsk |
B6.129-Boctm1Rsk Cdontm1Rsk | J:171767 | View | ||||
holoprosencephaly 11 |
Boctm1Rsk/Boctm1Rsk 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 |
Boctm2Rsk/Boctm2Rsk Cdontm1Rsk/Cdontm1Rsk |
B6.129-Boctm2Rsk Cdontm1Rsk | J:171767 | View | ||||
holoprosencephaly 11 |
Boctm2Rsk/Boctm2Rsk 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 | Glra1spd-ot9J/Glra1spd-ot9J | B6.Cg-Glra1spd-ot9J/GrsrJ | J:234690 | View | ||||
hyperekplexia 1 | Glra1spd/Glra1spd | involves: A/HeJ | J:33924 | View | ||||
hyperekplexia 1 | Glra1tm1Betz/Glra1tm1Betz | B6.129P2-Glra1tm1Betz | J:117236 | View | ||||
hyperekplexia 1 | Glra1tm1Rah/Glra1+ | involves: 129X1/SvJ * C57BL/6J | J:85341 | View | ||||
hyperekplexia 2 | Glrbspa/Glrbspa | Not Specified | J:33924 | View | ||||
hyperekplexia 3 | Slc6a5tm1Betz/Slc6a5tm1Betz | involves: 129P2/OlaHsd | J:86625 | View | ||||
hyperekplexia 3 | Slc6a5trsl/Slc6a5trsl | C57BL/6J-Slc6a5trsl/GrsrJ | J:235637 | View | ||||
hypochondroplasia | Fgfr3tm3.1Llm/Fgfr3+ | involves: C57BL/6N | J:338859 | 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 | 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 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 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 | Kiss1tm1Coll/Kiss1tm1Coll | involves: 129S/SvEv * 129S6/SvEvTac | J:122381 | View | ||||
hypogonadotropic hypogonadism 13 with or without anosmia | Kiss1tm1Rla/Kiss1tm1Rla | involves: 129S1/SvImJ | J:126704 | 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 | Tubb4aem1Avan/Tubb4aem1Avan | involves: C57BL/6 | J:291062 | View | ||||
hypomyelinating leukodystrophy 6 | Tubb4aJit/Tubb4a+ | FVB.B6-Tubb4aJit | J:321692 | View | ||||
hypomyelinating leukodystrophy 6 | Tubb4aJit/Tubb4aJit | FVB.B6-Tubb4aJit | J:321692 | 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 | ||||
IGSF1 deficiency syndrome | Igsf1tm1Zuk/Y | either: (involves: 129S6/SvEv * 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J) | J:190867 | View | ||||
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | Foxp3sf/Y | B6.Cg-Foxp3sf | J:167802 | View | ||||
immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | Foxp3sf/Y | either: 129Rl.Cg-Foxp3sf or (involves: 101/Rl * C3Hf/Rl * STOCK MR) | J:66734 | View | ||||
immunodeficiency 15A | Ikbkbem1Macc/Ikbkb+ | involves: C57BL/6NCrl | J:290616 | View | ||||
immunodeficiency 15A | Ikbkbem1Macc/Ikbkbem1Macc | involves: C57BL/6NCrl | J:290616 | View | ||||
immunodeficiency 73b with defective neutrophil chemotaxis and lymphopenia | Rac2em1Shl/Rac2+ | involves: C57BL/6 | J:276213 | View | ||||
immunodeficiency with hyper-IgM type 2 | Aicdaem1Jaych/Aicdaem1Jaych | involves: C57BL/6J | J:305843 | 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 | Alpltm1Jlm/Alpltm1Jlm | involves: 129S1/SvImJ * 129S2/SvPas * C57BL/6 | J:233260 | View | ||||
infantile hypophosphatasia | Alpltm1Sor/Alpltm1Sor | either: (involves: 129S7/SvEvBrd-Alpltm1Sor) or (involves: 129S7/SvEvBrd * C57BL/6) | J:28394 | View | ||||
inflammatory bowel disease 10 | Atg16l1Gt(BC0122)Wtsi/Atg16l1Gt(BC0122)Wtsi | involves: 129P2/OlaHsd * C57BL/6 | J:141419 | View | ||||
inflammatory bowel disease 10 | Atg16l1Gt(XR0164)Wtsi/Atg16l1Gt(XR0164)Wtsi | involves: 129P2/OlaHsd * C57BL/6 | J:141419 | View | ||||
inflammatory bowel disease 13 | Abcb1atm1Bor/Abcb1atm1Bor | FVB.129P2-Abcb1atm1Bor/TacImx | J:51190 | 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 | ||||
isolated mitochondrial myopathy | Chchd10em3Dpn/Chchd10em3Dpn | C57BL/6J-Chchd10em3Dpn | J:344465 | View | ||||
Johanson-Blizzard syndrome | Ubr1tm1Avar/Ubr1tm1Avar | involves: 129S1/Sv * C57BL/6 | J:105229 | View | ||||
Joubert syndrome 3 | Ahi1tm1Jgg/Ahi1tm1Jgg | involves: 129S1/Sv * 129X1/SvJ | J:172420 | View | ||||
Joubert syndrome 5 | Cep290Gt(CC0582)Wtsi/Cep290Gt(CC0582)Wtsi | 129P2/OlaHsd-Cep290Gt(CC0582)Wtsi | J:212182, J:226246 | View | ||||
Joubert syndrome 5 | Cep290tm1.1Jgg/Cep290tm1.1Jgg | involves: 129 | J:172420 | View | ||||
Joubert syndrome 6 | Tmem67tm1Dgen/Tmem67tm1Dgen | B6.129P2-Tmem67tm1Dgen | J:193837 | View | ||||
Joubert syndrome 7 | Rpgrip1ltm1Urt/Rpgrip1ltm1Urt | involves: 129S1/Sv * 129X1/SvJ | J:123018 | View | ||||
Joubert syndrome 17 | Cplane1b2b012Clo/Cplane1b2b012Clo | C57BL/6J-Cplane1b2b012Clo | J:223340 | View | ||||
Joubert syndrome 26 | KatnipGt(RRG309)Byg/KatnipGt(RRG309)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:239987 | 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 | ||||
Kartagener syndrome | Dnah5b2b002Clo/Dnah5b2b002Clo | C57BL/6J-Dnah5b2b002Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b016Clo/Dnah5b2b016Clo | C57BL/6J-Dnah5b2b016Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b601Clo/Dnah5b2b601Clo | C57BL/6J-Dnah5b2b601Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b1003Clo/Dnah5b2b1003Clo | C57BL/6J-Dnah5b2b1003Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b1134Clo/Dnah5b2b1134Clo | C57BL/6J-Dnah5b2b1134Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b1154Clo/Dnah5b2b1154Clo | C57BL/6J-Dnah5b2b1154Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b1537Clo/Dnah5b2b1537Clo | C57BL/6J-Dnah5b2b1537Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b1565Clo/Dnah5b2b1565Clo | C57BL/6J-Dnah5b2b1565Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b2395Clo/Dnah5b2b2395Clo | C57BL/6J-Dnah5b2b2395Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b2570Clo/Dnah5b2b2570Clo | C57BL/6J-Dnah5b2b2570Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b2925Clo/Dnah5b2b2925Clo | C57BL/6J-Dnah5b2b2925Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah5b2b3491Clo/Dnah5b2b3491Clo | C57BL/6J-Dnah5b2b3491Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah11b2b1727Clo/Dnah11b2b1727Clo | C57BL/6J-Dnah11b2b1727Clo | J:175213 | View | ||||
Kartagener syndrome | Dnah11b2b2349Clo/Dnah11b2b2349Clo | C57BL/6J-Dnah11b2b2349Clo | J:175213 | View | ||||
Kartagener syndrome | Dnai1b2b1526Clo/Dnai1b2b1526Clo | C57BL/6J-Dnai1b2b1526Clo | J:175213 | View | ||||
karyomegalic interstitial nephritis | Fan1tm1.1Jrou/Fan1tm1.1Jrou | involves: 129P2/OlaHsd | J:232403 | View | ||||
karyomegalic interstitial nephritis | Fan1tm1a(KOMP)Wtsi/Fan1tm1a(KOMP)Wtsi | 129S1.B6-Fan1tm1a(KOMP)Wtsi | J:242198 | 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 | ||||
Kohlschutter-Tonz syndrome | Rogditm1.2Ics/Rogditm1.2Ics | involves: C57BL/6N | J:344072 | View | ||||
Kufor-Rakeb syndrome | Atp13a2tm1.2Wtd/Atp13a2tm1.2Wtd | involves: 129 * C57BL/6 | J:221680 | View | ||||
Laron syndrome | Ghrtm1Arge/Ghrtm1Arge | involves: 129S/SvEv * C57BL/6J | J:66913 | View | ||||
Laron syndrome | Ghrtm1Jjk/Ghrtm1Jjk | involves: 129P2/OlaHsd * BALB/c | J:44604, J:157146 | View | ||||
Leber congenital amaurosis 1 | Gucy2ecpfl9/Gucy2ecpfl9 | B6;129P2-Gucy2ecpfl9/BocJ | J:269362 | View | ||||
Leber congenital amaurosis 1 |
Gucy2etm1Gar/Gucy2etm1Gar Gucy2ftm1Wbae/Gucy2ftm1Wbae |
involves: 129S6/SvEvTac | J:120903 | View | ||||
Leber congenital amaurosis 1 |
Gucy2etm1Gar/Gucy2etm1Gar Nrltm1Asw/Nrltm1Asw |
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6 | J:241970 | View | ||||
Leber congenital amaurosis 2 |
Cnga3tm1Biel/Cnga3tm1Biel Rpe65tm1Tmr/Rpe65tm1Tmr |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:71529 | 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 3 | Spata7tm1Mrd/Spata7tm1Mrd | involves: 129S7/SvEvBrd | J:216279 | View | ||||
Leber congenital amaurosis 3 |
Spata7tm1Mrd/Spata7tm2Mrd Tg(Crx-cre)1Tfur/0 |
involves: 129S7/SvEvBrd | J:279827 | View | ||||
Leber congenital amaurosis 4 | Aipl1tm1Mad/Aipl1tm1Mad | involves: 129S7/SvEvBrd | J:94655 | View | ||||
Leber congenital amaurosis 4 | Aipl1tm1Tili/Aipl1tm1Tili | involves: 129S4/SvJae * C57BL/6 | J:92601 | View | ||||
Leber congenital amaurosis 4 | Aipl1tm1Visu/Aipl1tm1Visu | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:92617 | 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 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 | Rpgrip1tm1Tili/Rpgrip1tm1Tili | involves: 129S4/SvJae * C57BL/6 | J:82755 | View | ||||
Leber congenital amaurosis 6 | Rpgrip1tvrm111/Rpgrip1tvrm111 | C57BL/6J-Rpgrip1tvrm111/Pjn | J:243745 | View | ||||
Leber congenital amaurosis 7 | Crxem2Smgc/Crx+ | C57BL/6J-Crxem2Smgc | J:343281 | View | ||||
Leber congenital amaurosis 7 | Crxrd23/Crxrd23 | B6.Cg-Crxrd23/BocJ | J:348234 | View | ||||
Leber congenital amaurosis 7 | CrxRip/Crx+ | C57BL/6J-CrxRip | J:203337 | View | ||||
Leber congenital amaurosis 7 | Crxtm1Clc/Crxtm1Clc | involves: 129S6/SvEvTac | J:58796 | View | ||||
Leber congenital amaurosis 8 | Crb1rd8/Crb1rd8 | STOCK Crb1rd8/J | J:171736 | 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 |
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 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 10 | Cep290rd16/Cep290rd16 | involves: BXD24/TyJ | J:125553 | View | ||||
Leber congenital amaurosis 10 | Cep290rd16/Cep290rd16 | involves: BXD24/TyJ * C57BL/6 | J:169232 | View | ||||
Leber congenital amaurosis 10 |
Cep290rd16/Cep290rd16 Nrltm1Asw/Nrltm1Asw |
involves: 129S1/Sv * 129X1/SvJ * BXD24/TyJ * C57BL/6 | J:169232 | 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 | ||||
Lesch-Nyhan syndrome | Hprt1b-m3/Hprt1b-m3 | B6.129P2-Hprt1b-m3 | J:17798 | View | ||||
Lesch-Nyhan syndrome | Hprt1b-m3/Y | B6.129P2-Hprt1b-m3 | J:17798, J:107966 | 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 | ||||
leukoencephalopathy with vanishing white matter |
Eif2b4tm1.1Vdk/Eif2b4+ Eif2b5tm1.1Vdk/Eif2b5tm1.1Vdk |
involves: C57BL/6 * C57BL/6J | J:234659 | View | ||||
leukoencephalopathy with vanishing white matter |
Eif2b4tm1.1Vdk/Eif2b4tm1.1Vdk Eif2b5tm1.1Vdk/Eif2b5+ |
involves: C57BL/6 * C57BL/6J | J:234659 | View | ||||
leukoencephalopathy with vanishing white matter |
Eif2b4tm1.1Vdk/Eif2b4tm1.1Vdk Eif2b5tm1.1Vdk/Eif2b5tm1.1Vdk |
involves: C57BL/6 * C57BL/6J | J:234659 | View | ||||
leukoencephalopathy with vanishing white matter | Eif2b5tm1.1Sidr/Eif2b5tm1.1Sidr | B6(Cg)-Eif2b5tm1.1Sidr | J:278928 | View | ||||
leukoencephalopathy with vanishing white matter | Eif2b5tm1.1Vdk/Eif2b5tm1.1Vdk | involves: C57BL/6 * C57BL/6J | J:234659 | View | ||||
leukoencephalopathy with vanishing white matter | Eif2b5tm1Itl/Eif2b5tm1Itl | involves: 129S/SvEv | J:192103 | View | ||||
leukoencephalopathy with vanishing white matter | Eif2b5tm1Itl/Eif2b5tm1Itl | involves: 129S/SvEv * C57BL * Swiss Webster | J:179801 | View | ||||
Li-Fraumeni syndrome | Trp53tm1Tyj/Trp53+ | involves: 129S2/SvPas | J:95316 | View | ||||
Li-Fraumeni syndrome | Trp53tm1Tyj/Trp53+ | involves: 129S2/SvPas * C57BL/6 | J:17728 | View | ||||
Li-Fraumeni syndrome | Trp53tm1Tyj/Trp53tm1Tyj | 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 | Trp53tm2.1Tyj/Trp53+ | involves: 129S4/SvJae | J:95316 | View | ||||
Li-Fraumeni syndrome | Trp53tm3.1Glo/Trp53+ | B6.129S7-Trp53tm3.1Glo | J:95318 | 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 3 | Scn5atm1.1Iba/Scn5a+ | involves: 129 * C57BL/6 | J:266290 | View | ||||
long QT syndrome 3 | Scn5atm1Care/Scn5a+ | FVB.129P2-Scn5atm1Care/Care | J:128657 | 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 |
Apctm1Rak/Apc+ Mlh1tm1Rak/Mlh1tm1Rak |
involves: 129P2/OlaHsd * C57BL/6 | J:53451 | View | ||||
Lynch syndrome | Mlh1tm1Rak/Mlh1tm1Rak | involves: 129P2/OlaHsd * C57BL/6 | J:53451 | View | ||||
Lynch syndrome | Msh2tm1Htr/Msh2tm1Htr | involves: 129P2/OlaHsd | J:45433 | View | ||||
Lynch syndrome |
Msh2tm1Htr/Msh2tm1Htr Tap1tm1Hpl/Tap1tm1Hpl |
involves: 129P2/OlaHsd * FVB | J:45433 | 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/Msh2tm2.1Rak Tg(Vil1-cre)20Syr/0 |
involves: 129/Sv * C57BL/6 * FVB/N * 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 | ||||
macrocephaly-autism syndrome | Ptentm1Engc/Ptentm1Engc | involves: CD-1 | J:210487 | View | ||||
macrocephaly-autism syndrome |
Ptentm2Mak/Ptentm2Mak Tg(Eno2-cre)39Jme/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:109635 | View | ||||
Mahvash Disease | Gcgrem2Smoc/Gcgrem2Smoc | C57BL/6J-Gcgrem2Smoc | J:300368 | View | ||||
mal de Meleda | Slurp1tm1.1Sgy/Slurp1tm1.1Sgy | involves: 129 * C57BL/6 | J:210836 | View | ||||
mal de Meleda | Slurp1tm1Lex/Slurp1tm1Lex | Not Specified | J:210836 | View | ||||
malignant hyperthermia | Ryr1em1Tmur/Ryr1+ | Not Specified | J:322211 | View | ||||
malignant hyperthermia | Ryr1tm1Slh/Ryr1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:105738 | View | ||||
malignant hyperthermia | Ryr1tm2.1Alle/Ryr1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:168222 | View | ||||
malignant hyperthermia | Ryr1tm3.1Alle/Ryr1+ | involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6 | J:303297 | View | ||||
malignant hyperthermia | Ryr1tm3.1Alle/Ryr1tm3.1Alle | involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6 | J:303297 | View | ||||
Marsili syndrome | Tg(Zfhx2*R1907K)#Jcox/0 | involves: C57BL/6 | J:266472 | View | ||||
Marsili syndrome | Zfhx2tm3Ymri/Zfhx2tm3Ymri | involves: 129P2/OlaHsd * C57BL/6 | J:266472 | View | ||||
MASA syndrome | L1camtm1Mtei/Y | either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * 129S/SvEv) | J:43838 | 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 | GckGena348/Gck+ | involves: BALB/c * C3H/He | J:90389 | 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 | Gckm1Rge/Gck+ | involves: C3HeB/FeJ | J:162903 | 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 | GckRgsc210/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | 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 | GckRgsc236/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/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 | GckRgsc475/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 | GckRgsc702/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 | GckRgsc735/Gck+ | involves: C57BL/6J * DBA/2J | J:88919 | 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 |
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/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 | Gcktm1.2Mgn/Gck+ | involves: 129S6/SvEvTac * C57BL/6 | J:51826 | 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 | Gcktm1Efr/Gck+ | involves: 129P2/OlaHsd * C57BL/6 | J:28756 | 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 | Gcktm1Tka/Gck+ | involves: 129X1/SvJ * ICR | J:30334 | 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 | 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 | Gcktm2Mgn/Gck+ | 129S6/SvEvTac-Gcktm2Mgn | J:121910 | View | ||||
maturity-onset diabetes of the young type 2 | Gcktm2Mgn/Gcktm2Mgn | 129S6/SvEvTac-Gcktm2Mgn | J:121910 | 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 4 | Pdx1tm1Ted/Pdx1+ | involves: 129P2/OlaHsd | J:82969 | View | ||||
Meckel syndrome | B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi | involves: C57BL/6N * CD-1 | J:178421 | 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 | ||||
methylmalonic acidemia and homocysteinemia cblX type | Hcfc1em1Poche/Y | C57BL/6J-Hcfc1em1Poche | J:317822 | 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)IR3.PV384Jtak/Smoc1Tn(sb-lacZ,GFP)IR3.PV384Jtak | involves: C3H * C57BL/6J * DBA/2 | J:169180 | 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 | ||||
microvillus inclusion disease | Myo5btm1a(KOMP)Wtsi/Myo5btm1a(KOMP)Wtsi | C57BL/6N-Myo5btm1a(KOMP)Wtsi | J:229427 | 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 | Bub1btm1Jvd/Bub1btm3.1Jvd | involves: 129S6/SvEvTac * C57BL/6 | J:293084 | View | ||||
mosaic variegated aneuploidy syndrome 1 | Bub1btm2.1Jvd/Bub1b+ | involves: 129S4/SvJae * 129S6/SvEvTac * C57BL/6 | J:194926 | 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/Fgfr3+ | 129S6.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3+ | B6.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3+ | CBACa.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw | 129S6.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw | B6.129P2-Fgfr3tm1.1Aomw | J:144356 | View | ||||
Muenke Syndrome | Fgfr3tm1.1Aomw/Fgfr3tm1.1Aomw | 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 | Men1tm1.1Gfk/Men1+ | involves: 129T2/SvEms * C57BL/6 | J:116086 | 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 |
Men1tm1Gfk/Men1tm1Gfk Tg(Ins2-cre)25Mgn/0 |
involves: 129T2/SvEms * C57BL/6 * C57BL/6J * DBA | J:89898 | 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 | Men1tm2.1Gfk/Men1+ | involves: 129T2/SvEms * C57BL/6 | J:116086 | View | ||||
multiple endocrine neoplasia type 2B | Rettm2.1Cos/Ret+ | involves: 129S1/Sv * C57BL/6J * FVB/N | J:60659 | View | ||||
multiple endocrine neoplasia type 2B | Rettm2.1Cos/Rettm2.1Cos | 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 B1 |
Pomt1tm1c(EUCOMM)Hmgu/Pomt1tm1c(EUCOMM)Hmgu Tg(Crx-cre)1Tfur/0 |
involves: C57BL/6N | J:263043 | 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/Des+ | involves: 129 * C57BL/6J | J:219616 | View | ||||
myofibrillar myopathy 1 | Destm1.1Ccrs/Destm1.1Ccrs | 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 | Cryabtm1.1Ady/Cryab+ | involves: 129X1/SvJ * C57BL/6 * C57BL/6J | J:171679 | View | ||||
myofibrillar myopathy 2 | Cryabtm1.1Ady/Cryabtm1.1Ady | involves: 129X1/SvJ * C57BL/6 * C57BL/6J | J:171679 | View | ||||
myofibrillar myopathy 2 | Tg(Myh6-Cryab*R120G)708Rbns/0 | FVB/N-Tg(Myh6-Cryab*R120G)708Rbns | J:133093 | 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 | ||||
Nance-Horan syndrome | NhsXcat/Nhs+ | involves: DBA/2 * T STOCK | J:19674, J:89306 | View | ||||
Nance-Horan syndrome | NhsXcat/NhsXcat | involves: DBA/2 * T STOCK | J:19674, J:89306 | View | ||||
Nance-Horan syndrome | NhsXcat/Y | involves: DBA/2 * T STOCK | J:19674, J:89306 | 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 | Nebtm1.1Hgra/Nebtm1.1Hgra | involves: C57BL/6 * C57BL/6J * SJL | J:206854 | 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 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 5A | 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/Nphp3pcy | involves: KK | J:91453 | View | ||||
nephronophthisis 3 | Nphp3pcy/Nphp3tm1Cbe | involves: C57BL/6 * CD-1 * KK/Upj | J:139258 | 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 | Spink5m1Btlr/Spink5m1Btlr | involves: C57BL/6J | J:183755 | 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 | 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 5 | Wdr45em1Wrst/Wdr45em1Wrst | involves: C57BL/6N * FVB | J:307284 | View | ||||
neurodegeneration with brain iron accumulation 5 | Wdr45em1Wrst/Y | involves: C57BL/6N * FVB | J:307284 | 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 dysmorphic facies and distal limb anomalies |
Bptftm1.1Cwu/Bptftm1.1Cwu Emx1tm1(cre)Krj/Emx1+ |
involves: 129S1/Sv * 129S2/SvPas * C57BL/6 | J:334252 | 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 | ||||
neurofibromatosis 1 |
Grin1tm1Stl/Grin1+ Nf1tm1Tyj/Nf1+ |
involves: 129S2/SvPas * C57BL/6J | J:38703 | View | ||||
neurofibromatosis 1 | Nf1Mhdadsk9/Nf1+ | involves: C3HeB/FeJ * C57BL/6 | J:269534 | View | ||||
neurofibromatosis 1 |
Nf1tm1.1Kest/Nf1tm1c(KOMP)Wtsi Tg(Dhh-cre)1Mejr/0 |
involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * C57BL/6NTac * FVB/N | J:234172 | View | ||||
neurofibromatosis 1 |
Nf1tm1c(KOMP)Wtsi/Nf1tm1c(KOMP)Wtsi Tg(Dhh-cre)1Mejr/0 |
involves: 129S4/SvJaeSor * C57BL/6 * C57BL/6N * FVB/N | J:234172 | View | ||||
neurofibromatosis 1 | Nf1tm1Cbr/Nf1tm1Cbr | involves: 129S1/Sv * C57BL/6 | J:68489 | View | ||||
neurofibromatosis 1 |
Nf1tm1Fcr/Nf1+ Trp53tm1Tyj/Trp53+ |
involves: 129S/SvEv * 129S2/SvPas * C57BL/6 | J:58877 | View | ||||
neurofibromatosis 1 | Nf1tm1Fcr/Nf1tm1Fcr | either: (involves: 129S/SvEv) or (involves: 129S/SvEv * C57BL/6J) | J:18048 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Fcr Tg(GFAP-cre)#Gtm/0 |
involves: 129S/SvEv * 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:165209 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:80323 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Fabp7-cre,-lacZ)3Gtm/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:138868 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Mpz-cre)94Imeg/0 |
involves: 129S1/Sv * 129X1/SvJ | J:80323 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Pax3-cre)1Joe/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL | J:80323 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Prrx1-cre)1Cjt/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * C57BL/6N * SJL/J | J:193350 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Prrx1-cre)1Cjt/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J | J:173779 | View | ||||
neurofibromatosis 1 |
Nf1tm1Par/Nf1tm1Par Tg(Syn1-cre)671Jxm/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:68558 | View | ||||
neurofibromatosis 1 | Nf1tm1Tyj/Nf1+ | involves: 129S2/SvPas * C57BL/6J | J:38703 | View | ||||
neurofibromatosis 1 |
Nf1tm1Tyj/Nf1+ Trp53tm1Tyj/Trp53+ |
involves: 129/Sv * C57BL/6 | J:58876 | View | ||||
neurohypophyseal diabetes insipidus | Avptm1Hari/Avp+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:147993 | View | ||||
neurohypophyseal diabetes insipidus | Avptm1Lja/Avp+ | involves: 129S1/Sv * 129X1/SvJ | J:148012 | View | ||||
neuronal ceroid lipofuscinosis 1 | Ppt1tm1.1Dprc/Ppt1tm1.1Dprc | involves: 129S6/SvEvTac * BALB/cJ * C57BL/6 | J:213552 | View | ||||
neuronal ceroid lipofuscinosis 1 | Ppt1tm1Aj/Ppt1tm1Aj | involves: 129S4/SvJae * C57BL/6 | J:95522 | View | ||||
neuronal ceroid lipofuscinosis 1 | Ppt1tm1Hof/Ppt1tm1Hof | involves: 129P2/OlaHsd * 129S2/SvPas * 129S6/SvEvTac * C57BL/6 | J:177265 | View | ||||
neuronal ceroid lipofuscinosis 2 | Tpp1m1J/Tpp1m1J | STOCK Tpp1m1J/GrsrJ | J:201119 | View | ||||
neuronal ceroid lipofuscinosis 2 | Tpp1tm1Plob/Tpp1tm1.1Plob | B6.129S1-Tpp1tm1Plob/Tpp1tm1.1Plob | J:136105 | View | ||||
neuronal ceroid lipofuscinosis 2 | Tpp1tm1Plob/Tpp1tm1Plob | B6.129S1-Tpp1tm1Plob | J:136105 | View | ||||
neuronal ceroid lipofuscinosis 2 | Tpp1tm1Plob/Tpp1tm1Plob | involves: 129S1/Sv * C57BL/6 | J:94884 | View | ||||
neuronal ceroid lipofuscinosis 3 | Cln3em1Dprc/Cln3em1Dprc | C57BL/6-Cln3em1Dprc | J:294634 | View | ||||
neuronal ceroid lipofuscinosis 3 | Cln3tm1.1Mem/Cln3tm1.1Mem | involves: 129S/SvEv * CD-1 | J:79615 | View | ||||
neuronal ceroid lipofuscinosis 3 | Cln3tm1Blda/Cln3tm1Blda | B6.129-Cln3tm1Blda | J:125194 | View | ||||
neuronal ceroid lipofuscinosis 3 | Cln3tm1Mkat/Cln3tm1Mkat | involves: 129X1/SvJ * C57BL/6J | J:57155 | View | ||||
neuronal ceroid lipofuscinosis 3 | Cln3tm1Nbm/Cln3tm1Nbm | 129S6/SvEvTac-Cln3tm1Nbm | J:109790 | View | ||||
neuronal ceroid lipofuscinosis 3 | Cln3tm1Nbm/Cln3tm1Nbm | involves: 129S6/SvEvTac * C57BL/6J | J:233445 | View | ||||
neuronal ceroid lipofuscinosis 3 | Cln3tm1Nbm/Cln3tm1Nbm | involves: 129S6/SvEvTac * NIH Black Swiss | J:58230 | View | ||||
neuronal ceroid lipofuscinosis 5 | Cln5tm1Pltn/Cln5tm1Pltn | involves: 129X1/SvJ * C57BL/6 | J:94383 | View | ||||
neuronal ceroid lipofuscinosis 6A | Cln6nclf/Cln6nclf | involves: C57BL/6J * C57BL/10J * C3HeB/FeJLe | J:73923 | View | ||||
neuronal ceroid lipofuscinosis 7 | Mfsd8tm1a(EUCOMM)Hmgu/Mfsd8tm1a(EUCOMM)Hmgu | involves: C57BL/6N | J:211608 | View | ||||
neuronal ceroid lipofuscinosis 8 | Cln8mnd/Cln8mnd | AK.B6(Cg)-Cln8mnd | J:56219 | View | ||||
neuronal ceroid lipofuscinosis 8 | Cln8mnd/Cln8mnd | B6.KB2/Rn-Cln8mnd | J:12816, J:56219 | View | ||||
neuronal ceroid lipofuscinosis 8 | Cln8mnd/Cln8mnd | involves: AKR/J * B6.KB2 | J:56219 | View | ||||
neuronal ceroid lipofuscinosis 8 | Cln8mnd/Cln8mnd | involves: B6.KB2 * C3H/HeJ | J:56219 | View | ||||
neuronal ceroid lipofuscinosis 10 | Ctsdm1J/Ctsdm1J | C3HeB/FeJ-Ctsdm1J/GrsrJ | J:229377 | View | ||||
neuronal ceroid lipofuscinosis 10 |
Ctsdtm1.1Thre/Ctsdtm1.1Thre Edil3Tg(Sox2-cre)1Amc/Edil3+ |
involves: C57BL/6 * C57BL/6N * CBA * SJL | J:227618 | View | ||||
neuronal ceroid lipofuscinosis 10 |
Ctsdtm1.1Thre/Ctsdtm1.1Thre Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * C57BL/6N * SJL | J:227618 | View | ||||
neuronal ceroid lipofuscinosis 10 | Ctsdtm1Cptr/Ctsdtm1Cptr | either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd) | J:138648 | View | ||||
Nijmegen breakage syndrome | Nbntm1.1Md/Nbntm1.1Md | involves: 129/Sv * 129P2/OlaHsd | J:93598 | View | ||||
Nijmegen breakage syndrome | Nbntm1Jpt/Nbntm1Jpt | involves: 129S7/SvEvBrd | J:75956 | View | ||||
Nijmegen breakage syndrome |
Nbntm1Md/Nbntm1Zqw Tg(Mx1-cre)1Cgn/0 |
involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA | J:93598 | View | ||||
Nijmegen breakage syndrome |
Nbntm1Nus/Nbntm2Nus Tg(CD19-cre/ERT2)1Cgn/0 |
Not Specified | J:96102 | View | ||||
Nijmegen breakage syndrome | Nbntm1Xu/Nbntm1Xu | Not Specified | J:75272 | View | ||||
Nijmegen breakage syndrome | Nbntm1Zqw/Nbn+ | involves: 129S2/SvPas * C57BL/6 | J:86563 | View | ||||
Nijmegen breakage syndrome | Nbntm1Zqw/Nbntm1Zqw | involves: 129S2/SvPas * C57BL/6 | J:86563 | View | ||||
non-syndromic X-linked intellectual developmental disorder 111 |
Slitrk2tm1.1Jwum/Y Tg(Nes-cre)1Atp/0 |
involves: C57BL/6J * FVB/N | J:342291 | View | ||||
non-syndromic X-linked intellectual disability | Gdi1tm1Toni/Y | B6N.129S7-Gdi1tm1Toni | J:142806 | View | ||||
non-syndromic X-linked intellectual disability 9 | Ftsj1tm1Tomik/Y | Not Specified | J:328916 | View | ||||
non-syndromic X-linked intellectual disability 30 | Pak3tm1.1Rpo/Y | B6.129S2(Cg)-Pak3tm1.1Rpo | J:292116 | View | ||||
non-syndromic X-linked intellectual disability 72 | Rab39btm1Pdad/Y | B6N.Cg-Rab39btm1Pdad | J:341888 | View | ||||
non-syndromic X-linked intellectual disability 98 | Nexmiftm1(KOMP)Wtsi/Y | B6J.B6N-Nexmiftm1(KOMP)Wtsi | J:283395 | View | ||||
Noonan syndrome 1 |
Emx1tm1(cre)Krj/Emx1+ Ptpn11tm6Bgn/Ptpn11+ |
B6.129S-Ptpn11tm6Bgn Emx1tm1(cre)Krj | J:242312 | View | ||||
Noonan syndrome 1 | Ptpn11tm1Bgn/Ptpn11+ | involves: 129S4/SvJae * C57BL/6J | J:91609 | View | ||||
Noonan syndrome 1 | Tg(Myh7-Ptpn11*Q79R)11Rbns/0 | FVB.Cg-Tg(Myh7-Ptpn11*Q79R)11Rbns | J:123963 | View | ||||
Noonan syndrome 3 | Krastm4.1Bbd/Krastm4.1Bbd | involves: 129S1/Sv * 129S2/SvPas * 129X1/SvJ * C57BL/6J * FVB/N | J:223433 | View | ||||
Noonan syndrome 4 | Sos1tm1.2Rak/Sos1+ | involves: 129S/Sv * C57BL/6 * FVB/N * SJL | J:171873 | View | ||||
Noonan syndrome 4 | Sos1tm1.2Rak/Sos1tm1.2Rak | involves: 129S/Sv * C57BL/6 * FVB/N * SJL | J:171873 | View | ||||
Noonan syndrome 5 | Raf1tm1.1Bgn/Raf1+ | involves: 129S6/SvEvTac * C57BL/6NCr | J:172034 | View | ||||
Noonan syndrome 5 | Raf1tm2.1Ara/Raf1tm2.1Ara | involves: 129S6/SvEvTac * C57BL/6NCr | J:189143 | View | ||||
Noonan syndrome 8 | Rit1tm1.1Tumg/Rit1+ | B6.Cg-Rit1tm1.1Tumg | J:277548 | View | ||||
Noonan syndrome 10 | Lztr1tm1a(EUCOMM)Wtsi/Lztr1+ | involves: C57BL/6N | J:268690 | View | ||||
Norrie disease | Ndptm1Wbrg/Y | involves: 129/Sv * 129P2/OlaHsd * C57BL/6 * CBA/CaJ * CD-1 | J:77024 | View | ||||
Norrie disease | Ndptm1Wbrg/Y | involves: 129P2/OlaHsd * C57BL/6 | J:30902 | View | ||||
nuclear type mitochondrial complex I deficiency 20 |
Acad9tm1c(KOMP)Wtsi/Acad9tm1c(KOMP)Wtsi Tg(ACTA1-cre)79Jme/0 |
involves: C57BL/6J * C57BL/6N * FVB/N * SJL | J:326969 | View | ||||
nuclear type mitochondrial complex I deficiency 20 |
Acad9tm1c(KOMP)Wtsi/Acad9tm1c(KOMP)Wtsi Tg(Myh6-cre)2182Mds/0 |
involves: C57BL/6N * FVB/N | J:326969 | View | ||||
oculocutaneous albinism | Tyrc-2J/Tyrc-2J | B6(Cg)-Tyrc-2J/J | J:178454 | View | ||||
oculocutaneous albinism | Tyrc-h/Tyrc-h | B6.Cg-Tyrc-h/J | J:178454 | View | ||||
Oguchi disease-2 | Grk1tm1Citb/Grk1tm1Citb | involves: 129X1/SvJ * C57BL/6 | J:54021 | View | ||||
Opitz GBBB syndrome | Mid1tm1Mero/Y | B6.Cg-Mid1tm1Mero | J:157828 | View | ||||
orofaciodigital syndrome I |
Ofd1tm2.1Bfra/Ofd1+ Tg(CAG-cre)1Nagy/0 |
involves: 129S2/SvPas | J:106035 | View | ||||
orofaciodigital syndrome I |
Ofd1tm2.1Bfra/Y Tg(CAG-cre)1Nagy/0 |
involves: 129S2/SvPas | J:106035 | View | ||||
osteogenesis imperfecta type 1 | Col1a1Mov13/Col1a1+ | involves: C57BL/6 | J:107045 | View | ||||
osteogenesis imperfecta type 2 | Col1a1Aga2/Col1a1+ | involves: C3HeB/FeJ * C57BL/6J | J:129569 | View | ||||
osteogenesis imperfecta type 2 | Col1a1tm1Jcm/Col1a1+ | either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1) | J:59168 | View | ||||
osteogenesis imperfecta type 3 | Col1a1Aga2/Col1a1+ | C3HeB/FeJ-Col1a1Aga2 | J:185988 | View | ||||
osteogenesis imperfecta type 3 | Col1a2oim/Col1a2oim | B6C3Fe a/a-Col1a2oim/J | J:38013 | View | ||||
osteogenesis imperfecta type 3 | Col1a2oim/Col1a2oim | involves: C3H/HeJ * C57BL/6JLe | J:4348 | View | ||||
osteogenesis imperfecta type 4 | Col1a1M1Jrt/Col1a1+ | involves: C3H/HeJ * C57BL/6J * FVB/NJ | J:216423 | View | ||||
osteogenesis imperfecta type 4 | Col1a1M1Jrt/Col1a1+ | involves: C57BL/6 * FVB/N | J:228439 | View | ||||
osteogenesis imperfecta type 4 | Col1a1tm1.1Jcm/Col1a1+ | either: (involves: 129X1/SvJ * C3H/HeJ) or (involves: 129X1/SvJ * CD-1) | J:59168 | View | ||||
osteogenesis imperfecta type 5 | Tg(Col1a1-Ifitm5*)1Brle/0 | involves: FVB/N | J:233366 | View | ||||
osteogenesis imperfecta type 6 | Serpinf1tm1Craw/Serpinf1tm1Craw | Not Specified | J:230409 | View | ||||
osteogenesis imperfecta type 7 | Crtaptm1Brle/Crtaptm1Brle | involves: 129S7/SvEvBrd | J:116096 | View | ||||
osteogenesis imperfecta type 8 | P3h1tm1Dgen/P3h1tm1Dgen | involves: C57BL/6 | J:163884 | View | ||||
osteogenesis imperfecta type 9 | PpibGt(RST139)Byg/PpibGt(RST139)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:226318 | View | ||||
osteogenesis imperfecta type 9 | Ppibtm1.1Rjb/Ppibtm1.1Rjb | Not Specified | J:161748 | View | ||||
osteogenesis imperfecta type 10 |
Serpinh1tm2Kzn/Serpinh1tm2Kzn Tg(Col2a1-cre)1Bhr/0 |
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL | J:197791 | View | ||||
osteoporosis-pseudoglioma syndrome | Lrp5tm1Grw/Lrp5tm1Grw | involves: 129S1/Sv * 129X1/SvJ | J:213541 | View | ||||
osteoporosis-pseudoglioma syndrome | Lrp5tm1Kry/Lrp5+ | either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J) | J:75973 | View | ||||
osteoporosis-pseudoglioma syndrome | Lrp5tm1Kry/Lrp5tm1Kry | either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J) | J:75973 | View | ||||
otospondylomegaepiphyseal dysplasia, autosomal recessive | Col11a2tm1Mne/Col11a2tm1Mne | FVB.129-Col11a2tm1Mne | J:71948 | View | ||||
pachyonychia congenita | Krt16tm1(KOMP)Vlcg/Krt16tm1(KOMP)Vlcg | C57BL/6-Krt16tm1(KOMP)Vlcg | J:184621 | View | ||||
Pallister-Hall syndrome | Gli3tm1Urt/Gli3tm1Urt | involves: 129P2/OlaHsd * C57BL/6 | J:76496 | View | ||||
palmoplantar keratoderma-esophageal carcinoma syndrome | Rhbdf2cub/Rhbdf2cub | B6.Cg-Rhbdf2cub | J:250259 | View | ||||
palmoplantar keratoderma-esophageal carcinoma syndrome | Rhbdf2cub/Rhbdf2cub | MRL.Cg-Rhbdf2cub | J:250259 | View | ||||
palmoplantar keratoderma-esophageal carcinoma syndrome | Rhbdf2em2Mvw/Rhbdf2em2Mvw | C57BL/6J-Rhbdf2em2Mvw/Mvw | J:244160 | View | ||||
Parkinson's disease 1 | Sncatm1.1Koks/Snca+ | either: B6.129P2-Sncatm1.1Koks or (involves: 129P2/OlaHsd * C57BL/6) | J:201391 | View | ||||
Parkinson's disease 1 |
Sncatm1Nbm/Sncatm1Nbm Tg(SNCA*A30P)1Nbm/Tg(SNCA*A30P)1Nbm Tg(SNCA*A30P)2Nbm/Tg(SNCA*A30P)2Nbm |
involves: 129S6/SvEvTac * FVB/N | J:156741 | View | ||||
Parkinson's disease 1 |
Sncatm1Nbm/Sncatm1Nbm Tg(SNCA*A53T)1Nbm/Tg(SNCA*A53T)1Nbm Tg(SNCA*A53T)2Nbm/Tg(SNCA*A53T)2Nbm |
involves: 129S6/SvEvTac * FVB/N | J:156741 | View | ||||
Parkinson's disease 1 | Sncatm1Rosl/Sncatm1Rosl | involves: 129X1/SvJ * C57BL/6 | J:60151 | View | ||||
Parkinson's disease 1 |
Sncatm1Rosl/Sncatm1Rosl Tg(SNCA)OVX37Rwm/0 |
B6.Cg-Tg(SNCA)OVX37Rwm Sncatm1Rosl | J:201991 | View | ||||
Parkinson's disease 1 |
Sncatm1Rosl/Sncatm1Rosl Tg(SNCA*A30P)192Rwm/0 |
B6.Cg-Sncatm1Rosl Tg(SNCA*A30P)#Rwm | J:201961 | View | ||||
Parkinson's disease 2 | Prkntm1Ccs/Prkntm1Ccs | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:168847 | View | ||||
Parkinson's disease 2 | Prkntm1Roo/Prkntm1Roo | either: 129S2/SvPas or (involves: 129S2/SvPas * C57BL/6) | J:85561 | View | ||||
Parkinson's disease 2 | Prkntm1Roo/Prkntm1Roo | involves: 129S2/SvPas | J:125148 | View | ||||
Parkinson's disease 2 | Prkntm1Shn/Prkntm1Shn | involves: 129S4/SvJae | J:86377 | View | ||||
Parkinson's disease 2 | Prkntm1Tmd/Prkntm1Tmd | involves: C57BL/6 | J:91487 | View | ||||
Parkinson's disease 2 |
Prkntm1Ykt/Prkntm1Ykt Tg(PDGFB-GPR37)20Ryot/0 |
involves: 129P2/OlaHsd * C57BL/6 | J:140326 | View | ||||
Parkinson's disease 2 |
Prkntm1Ykt/Prkntm1Ykt Tg(PDGFB-GPR37)20Ryot/Tg(PDGFB-GPR37)20Ryot |
involves: 129P2/OlaHsd * C57BL/6 | J:140326 | View | ||||
Parkinson's disease 2 |
Prkntm1Ykt/Prkntm1Ykt Tg(Prp-GPR37)1Ryot/0 |
involves: 129P2/OlaHsd * C3H * C57BL/6 | J:140326 | View | ||||
Parkinson's disease 2 |
Prkntm1Ykt/Prkntm1Ykt Tg(Prp-GPR37)1Ryot/Tg(Prp-GPR37)1Ryot |
involves: 129P2/OlaHsd * C3H * C57BL/6 | J:140326 | View | ||||
Parkinson's disease 4 | Tg(Thy1-Snca)1S13Putt/? | involves: C57BL/6 | J:177661 | View | ||||
Parkinson's disease 6 | Pink1tm1.1Wrst/Pink1tm1.1Wrst | involves: 129S2/SvPas * BALB/cJ * C57BL/6J | J:183290 | View | ||||
Parkinson's disease 6 | Pink1tm1Aub/Pink1tm1Aub | involves: 129S/SvEv | J:150206 | View | ||||
Parkinson's disease 6 | Pink1tm1Hbu/Pink1tm1Hbu | involves: 129S7/SvEvBrd * C57BL/6 | J:169471 | View | ||||
Parkinson's disease 6 | Pink1tm1Shn/Pink1tm1Shn | involves: 129S4/SvJae * C57BL/6 | J:122728 | View | ||||
Parkinson's disease 7 | Park7tm1Cai/Park7tm1Cai | involves: 129X1/SvJ * C57BL/6 | J:141628 | View | ||||
Parkinson's disease 7 | Park7tm1Dsp/Park7tm1Dsp | B6.129P2-Park7tm1Dsp | J:190315 | View | ||||
Parkinson's disease 7 | Park7tm1Shn/Park7tm1Shn | involves: 129 * C57BL/6 | J:98436 | View | ||||
Parkinson's disease 7 | Park7tm1Xz/Park7tm1Xz | involves: 129P2/OlaHsd * C57BL/6J | J:99905 | View | ||||
Parkinson's disease 8 | Tg(Lrrk2*G2019S)2Yue/0 | involves: C3H * C57BL/6 * C57BL/6J | J:157931 | View | ||||
Parkinson's disease 14 | Pla2g6tm1.1Hlw/Pla2g6tm1.1Hlw | involves: 129 * C57BL/6J | J:317126 | View | ||||
Parkinson's disease 17 | Vps35Gt(RRK261)Byg/Vps35+ | B6.129P2-Vps35Gt(RRK261)Byg | J:225806 | View | ||||
Parkinson's disease 17 | Vps35tm1.1Hlw/Vps35+ | involves: 129S/SvEv * C57BL/6J | J:329507 | View | ||||
paroxysmal nonkinesigenic dyskinesia 1 | Tg(Pnkd*A7V*A9V,-DsRed)671Ljp/0 | B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)671Ljp | J:192798 | View | ||||
paroxysmal nonkinesigenic dyskinesia 1 | Tg(Pnkd*A7V*A9V,-DsRed)704Ljp/0 | B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)704Ljp | J:192798 | View | ||||
PCWH syndrome | Sox10gt/Sox10gt | GT/Le | J:216967 | View | ||||
Pelger-Huet anomaly | Lbric-J/Lbric-J | involves: 129S4/SvJae * C57BL/6 | J:143838 | View | ||||
Pelizaeus-Merzbacher disease | Dp(XTceal3-Plp1)1Gmh/Y | involves: 129S7/SvEvBrd * C57BL/6 | J:199809 | View | ||||
Pelizaeus-Merzbacher disease | Plp1jp-msd/Y | involves: BALB/c * C3H * C57BL/6 * C57BL/10 | J:121540 | View | ||||
Pelizaeus-Merzbacher disease | Plp1jp-rsh/Y | involves: C3H * C57BL/6 * STOCK Rb(1.3)1Bnr | J:121540 | View | ||||
Pelizaeus-Merzbacher disease | Plp1tm1Frca/Y | B6.129-Plp1tm1Frca | J:143305 | View | ||||
Pelizaeus-Merzbacher disease | Plp1tm1Kan/? | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:146665 | View | ||||
Pelizaeus-Merzbacher disease | Tg(Plp)66Kan/0 | B6NCrl.Cg-Tg(Plp)66Kan | J:156106 | View | ||||
Pelizaeus-Merzbacher disease | Tg(Plp)66Kan/Tg(Plp)66Kan | B6NCrl.Cg-Tg(Plp)66Kan | J:156106 | View | ||||
Pelizaeus-Merzbacher disease | Tg(Plp)72Kan/Tg(Plp)72Kan | B6N.Cg-Tg(Plp)72Kan | J:229229 | View | ||||
Pendred Syndrome | Slc26a4em1Jgao/Slc26a4em1Jgao | involves: CBA/CaJ | J:291230 | View | ||||
Pendred Syndrome | Slc26a4pdsm/Slc26a4pdsm | BXA7/PgnJ-Slc26a4pdsm/J | J:121997 | View | ||||
Pendred Syndrome | Slc26a4tm1Egr/Slc26a4tm1Egr | either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * Black Swiss) | J:67072 | View | ||||
Pendred Syndrome | Slc26a4tm1Egr/Slc26a4tm1Egr | involves: 129S6/SvEvTac | J:116301, J:101834, J:121442 | View | ||||
permanent neonatal diabetes mellitus |
Gt(ROSA)26Sortm1(CAG-Kcnj11*,-GFP)Nich/Gt(ROSA)26Sor+ Tg(Ins2-cre)23Herr/0 |
involves: C57BL/6 * CBA/J | J:146650 | View | ||||
permanent neonatal diabetes mellitus |
Gt(ROSA)26Sortm1(Kcnj11*V59M)Fmas/Gt(ROSA)26Sor+ Tg(Ins2-cre)23Herr/0 |
involves: 129S4/SvJae * C57BL/6 | J:144715 | View | ||||
permanent neonatal diabetes mellitus |
Gt(ROSA)26Sortm1(Kcnj11*V59M)Fmas/Gt(ROSA)26Sor+ Tg(Nes-cre)1Kln/0 |
involves: 129S4/SvJae * C57BL/6 * SJL | J:162008 | View | ||||
permanent neonatal diabetes mellitus | Ins2Akita/Ins2Akita | C57BL/6-Ins2Akita | J:47883 | View | ||||
peroxisomal acyl-CoA oxidase deficiency | Acox1tm1Jkr/Acox1tm1Jkr | involves: 129P2/OlaHsd * C57BL/6J | J:35794 | View | ||||
Perrault syndrome | ClppGt(IST11134F10)Tigm/ClppGt(IST11134F10)Tigm | involves: C57BL/6N | J:203140 | View | ||||
Perrault syndrome | ClppGt(IST13563G11)Tigm/ClppGt(IST13563G11)Tigm | involves: C57BL/6N | J:203140 | View | ||||
Pfeiffer syndrome | Fgfr1tm1Led/Fgfr1tm1Led | involves: 129S4/SvJae * NIH Black Swiss | J:22118 | View | ||||
Pfeiffer syndrome | Fgfr1tm2.1Cxd/Fgfr1+ | D2.129S6(Cg)-Fgfr1tm2.1Cxd | J:228708 | View | ||||
Pfeiffer syndrome | Fgfr2tm2.3Dsn/Fgfr2+ | involves: 129 * C57BL/6 * FVB/N | J:72517 | View | ||||
PHARC syndrome | Abhd12tm1Crv/Abhd12tm1Crv | involves: C57BL/6 | J:193716 | View | ||||
piebaldism | KitWps/KitWps | involves: C57BL/6J * CBA/CaJ | J:196572 | View | ||||
Pierpont syndrome | Tbl1xr1em2H/Tbl1xr1em2H | C57BL/6J-Tbl1xr1em2H | J:335355 | View | ||||
Pierson syndrome | Lamb2npht/Lamb2npht | involves: C57BL/6 | J:208069 | View | ||||
Pierson syndrome | Lamb2tm1Jrs/Lamb2tm1Jrs | involves: 129S1/Sv * 129X1/SvJ | J:106005 | View | ||||
Pitt-Hopkins syndrome | Tcf4em1Bdph/? | involves: C57BL/6 * C57BL/6J | J:254983 | View | ||||
Pitt-Hopkins syndrome | Tcf4em2Bdph/? | involves: C57BL/6 * C57BL/6J | J:254983 | View | ||||
Pitt-Hopkins syndrome | Tcf4tm1a(EUCOMM)Wtsi/Tcf4+ | involves: C57BL/6N | J:265025 | View | ||||
Pitt-Hopkins syndrome |
Tcf4tm1Hmb/Tcf4+ Tg(Nes-cre)1Kln/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:254983 | View | ||||
Pitt-Hopkins syndrome |
Tcf4tm1Hmb/Tcf4+ Tmem163Tg(ACTB-cre)2Mrt/Tmem163+ |
involves: 129P2/OlaHsd * C57BL/6 * FVB/N | J:254983 | View | ||||
Pitt-Hopkins syndrome | Tcf4tm1Zhu/Tcf4+ | involves: 129P2/OlaHsd * 129S1/SvImJ * C57BL/6J | J:239016 | View | ||||
platelet-type bleeding disorder 8 | P2ry12tm1Cjf/P2ry12tm1Cjf | involves: 129 | J:70017 | View | ||||
platelet-type bleeding disorder 8 | P2ry12tm1Pcon/P2ry12tm1Pcon | involves: 129P2/OlaHsd * C57BL/6 | J:84917 | View | ||||
platelet-type bleeding disorder 10 | Cd36tm1Mfe/Cd36tm1Mfe | involves: 129S1/Sv * C57BL/6 | J:56081 | View | ||||
platelet-type bleeding disorder 16 | Itga2btm1Tlr/Itga2btm1Tlr | either: (involves: 129S1/Sv * 129X1/SvJ * BALB/c) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:63961 | View | ||||
platelet-type bleeding disorder 16 | Itgb3tm1Hyn/Itgb3tm1Hyn | involves: 129S2/SvPas * C57BL/6 | J:52262 | View | ||||
polycystic kidney disease 1 |
Gpsm1tm1.1Lajb/Gpsm1tm1.1Lajb Pkd1tm1.1Fqi/Pkd1tm1.1Fqi |
involves: 129S6/SvEvTac | J:193175 | View | ||||
polycystic kidney disease 1 | Pkd1b2b1585Clo/Pkd1b2b1585Clo | C57BL/6J-Pkd1b2b1585Clo | J:175213 | View | ||||
polycystic kidney disease 1 | Pkd1tm1.1Fqi/Pkd1tm1.1Fqi | involves: 129S6/SvEvTac | J:193175 | View | ||||
polycystic kidney disease 1 | Pkd1tm1.1Pcha/Pkd1tm1.1Pcha | involves: 129S1/Sv * C57BL/6 | J:193544 | View | ||||
polycystic kidney disease 1 |
Pkd1tm1.1Pcha/Pkd1tm2Som Tg(Cdh16-cre)91Igr/0 |
involves: 129 * 129S4/SvJae * C57BL/6 * ICR | J:244067 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Bdgz/Pkd1+ | involves: 129S1/Sv * 129X1/SvJ | J:130086 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Djmp/Pkd1tm1Djmp | involves: 129P2/OlaHsd * C57BL/6 | J:94582 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Ggg/Pkd1tm1Ggg | Not Specified | J:76062 | View | ||||
polycystic kidney disease 1 |
Pkd1tm1Gztn/Pkd1tm1Gztn Gt(ROSA)26Sortm9(cre/ESR1)Arte/Gt(ROSA)26Sor+ |
involves: 129S/Sv * 129S7/SvEvBrd * C57BL/6 | J:162080 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Jzh/Pkd1+ | either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c) | J:43193, J:52573, J:72627 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Jzh/Pkd1tm1Jzh | either: (involves: 129S4/SvJae * C57BL/6) or (involves: 129S4/SvJae * BALB/c) | J:43193, J:72627, J:81443 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Rsa/Pkd1+ | involves: 129S4/SvJaeSor | J:72238 | View | ||||
polycystic kidney disease 1 | Pkd1tm1Shh/Pkd1tm1.1Pcha | involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 | J:193544 | View | ||||
polycystic kidney disease 1 |
Pkd1tm1Som/Pkd1+ Tg(Pkd1*)39Mtru/0 |
involves: 129/Sv * C57BL/6J * CBA/J * SJL | J:198147 | View | ||||
polycystic kidney disease 1 | Pkd1tm2.1Ggg/Pkd1tm2.1Ggg | involves: 129S4/SvJae * Black Swiss * C57BL/6 | J:103719 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Col1a1-cre)1Bek/0 |
involves: 129S4/SvJae * CD-1 | J:191967 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Hoxb7-cre)13Amc/0 |
involves: 129S4/SvJae * C57BL/6 | J:171619 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(MMTV-cre)4Mam/0 |
involves: 129S4/SvJae * FVB | J:103719 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Ggg/Pkd1tm2Ggg Tg(Nes-cre)Wme/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:185855 | View | ||||
polycystic kidney disease 1 | Pkd1tm2Jzh/Pkd1+ | either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6) | J:72627 | View | ||||
polycystic kidney disease 1 | Pkd1tm2Jzh/Pkd1tm2Jzh | either: (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6) | J:72627 | View | ||||
polycystic kidney disease 1 | Pkd1tm2Jzh/Pkd1tm2Jzh | involves: 129S4/SvJae * C57BL/6 | J:140012 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Som/Pkd1tm2.1Som Tg(Cdh16-cre)91Igr/0 |
involves: C57BL/6 * ICR * SJL | J:135301 | View | ||||
polycystic kidney disease 1 |
Pkd1tm2Som/Pkd1tm2Som Tg(Cdh16-cre)91Igr/0 |
involves: 129S4/SvJae * C57BL/6 * ICR | J:244067 | View | ||||
polycystic kidney disease 1 | Pkd1tm3.1Jzh/Pkd1tm3.1Jzh | involves: 129P2/OlaHsd * C57BL/6 | J:140012 | View | ||||
polycystic kidney disease 1 |
Pkd1tm3Jzh/Pkd1tm3Jzh Tg(Ggt1-cre)M3Egn/0 |
involves: 129P2/OlaHsd * C57BL/6 * SJL | J:140012 | View | ||||
polycystic kidney disease 1 | Tg(Pkd1*)39Mtru/0 | involves: C57BL/6J * CBA/J | J:198147 | View | ||||
polycystic kidney disease 2 | Pkd2tm1Dwo/Pkd2tm1Dwo | either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:77401 | View | ||||
polycystic kidney disease 2 | Pkd2tm1Som/Pkd2+ | involves: 129/Sv * C57BL/6J * SJL | J:47035 | View | ||||
polycystic kidney disease 2 | Pkd2tm1Som/Pkd2tm1Som | involves: 129/Sv * C57BL/6J * SJL | J:47035 | View | ||||
polycystic kidney disease 2 | Pkd2tm1Som/Pkd2tm2Som | involves: 129/Sv * C57BL/6J * SJL | J:47035 | View | ||||
polycystic kidney disease 2 | Pkd2tm2Som/Pkd2+ | involves: 129/Sv * C57BL/6J * SJL | J:59314 | View | ||||
polycystic kidney disease 2 | Pkd2tm2Som/Pkd2tm2Som | involves: 129/Sv * C57BL/6J * SJL | J:59314 | View | ||||
polycystic kidney disease 2 |
Pkd2tm3Som/Pkd2tm3Som Tg(Pkhd1-cre)1Igr/0 |
involves: 129S4/SvJae * C57BL/6 | J:244067 | View | ||||
polycystic kidney disease 4 | Pkhd1em1Mrug/Pkhd1+ | involves: C57BL/6J | J:281464 | View | ||||
polycystic kidney disease 4 | Pkhd1em1Mrug/Pkhd1em1Mrug | involves: C57BL/6J | J:281464 | View | ||||
polycystic liver disease |
Prkcshtm1Som/Prkcshtm1Som Tg(CAG-cre/Esr1*)1Lbe/0 |
involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6 | J:188763 | View | ||||
pontocerebellar hypoplasia type 14 | Ppil1em3Jgg/Ppil1em3Jgg | C57BL/6-Ppil1em3Jgg | J:300487 | View | ||||
pontocerebellar hypoplasia type 14 | Ppil1em4Jgg/Ppil1em4Jgg | C57BL/6-Ppil1em4Jgg | J:300487 | View | ||||
popliteal pterygium syndrome | Irf6Gt(OST398253)Lex/Irf6Gt(OST398253)Lex | involves: 129S5/SvEvBrd * C57BL/6 | J:115343 | View | ||||
popliteal pterygium syndrome | Irf6tm1Mjd/Irf6+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:116077 | View | ||||
primary autosomal recessive microcephaly 2 with or without cortical malformations | Wdr62tm1.1Jfch/Wdr62tm1.1Jfch | involves: 129S1/SvImJ * C57BL/6N | J:282438 | View | ||||
primary ciliary dyskinesia | Daw1b2b1116Clo/Daw1b2b1116Clo | C57BL/6J-Daw1b2b1116Clo | J:175213 | View | ||||
primary ciliary dyskinesia | Daw1b2b1584Clo/Daw1b2b1584Clo | C57BL/6J-Daw1b2b1584Clo | J:175213 | View | ||||
primary ciliary dyskinesia 1 | Dnai1b2b284Clo/Dnai1b2b284Clo | C57BL/6J-Dnai1b2b284Clo | J:175213 | View | ||||
primary ciliary dyskinesia 1 | Dnai1b2b1526Clo/Dnai1b2b1526Clo | C57BL/6J-Dnai1b2b1526Clo | J:175213 | View | ||||
primary ciliary dyskinesia 1 |
Dnai1tm1.1Leo/Dnai1tm1.1Leo Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sor+ |
involves: 129 * C57BL/6 | J:155730 | View | ||||
primary ciliary dyskinesia 2 | Dnaaf3b2b1739Clo/Dnaaf3b2b1739Clo | C57BL/6J-Dnaaf3b2b1739Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b002Clo/Dnah5b2b002Clo | C57BL/6J-Dnah5b2b002Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b016Clo/Dnah5b2b016Clo | C57BL/6J-Dnah5b2b016Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b601Clo/Dnah5b2b601Clo | C57BL/6J-Dnah5b2b601Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b1003Clo/Dnah5b2b1003Clo | C57BL/6J-Dnah5b2b1003Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b1134Clo/Dnah5b2b1134Clo | C57BL/6J-Dnah5b2b1134Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b1154Clo/Dnah5b2b1154Clo | C57BL/6J-Dnah5b2b1154Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b1537Clo/Dnah5b2b1537Clo | C57BL/6J-Dnah5b2b1537Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b1565Clo/Dnah5b2b1565Clo | C57BL/6J-Dnah5b2b1565Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b2395Clo/Dnah5b2b2395Clo | C57BL/6J-Dnah5b2b2395Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b2570Clo/Dnah5b2b2570Clo | C57BL/6J-Dnah5b2b2570Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b2925Clo/Dnah5b2b2925Clo | C57BL/6J-Dnah5b2b2925Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5b2b3491Clo/Dnah5b2b3491Clo | C57BL/6J-Dnah5b2b3491Clo | J:175213 | View | ||||
primary ciliary dyskinesia 3 | Dnah5hlb612/Dnah5hlb612 | involves: C57BL/6J | J:130755 | View | ||||
primary ciliary dyskinesia 3 | Dnah5Tg1Htz/Dnah5Tg1Htz | involves: C57BL/6 * CBA/J | J:76189 | View | ||||
primary ciliary dyskinesia 7 | Dnah11b2b598Clo/Dnah11b2b598Clo | C57BL/6J-Dnah11b2b598Clo | J:175213 | View | ||||
primary ciliary dyskinesia 7 | Dnah11b2b1203Clo/Dnah11b2b1203Clo | C57BL/6J-Dnah11b2b1203Clo | J:175213 | View | ||||
primary ciliary dyskinesia 7 | Dnah11b2b1279Clo/Dnah11b2b1279Clo | C57BL/6J-Dnah11b2b1279Clo | J:175213 | View | ||||
primary ciliary dyskinesia 7 | Dnah11b2b1289Clo/Dnah11b2b1289Clo | C57BL/6J-Dnah11b2b1289Clo | J:175213 | View | ||||
primary ciliary dyskinesia 7 | Dnah11b2b1727Clo/Dnah11b2b1727Clo | C57BL/6J-Dnah11b2b1727Clo | J:175213 | View | ||||
primary ciliary dyskinesia 7 | Dnah11b2b1775Clo/Dnah11b2b1775Clo | C57BL/6J-Dnah11b2b1775Clo | J:175213 | View | ||||
primary ciliary dyskinesia 7 | Dnah11b2b2349Clo/Dnah11b2b2349Clo | C57BL/6J-Dnah11b2b2349Clo | J:175213 | View | ||||
primary ciliary dyskinesia 7 | Dnah11iv/Dnah11iv | involves: C3H | J:212 | View | ||||
primary ciliary dyskinesia 10 | Dnaaf2tm1.1(KOMP)Vlcg/Dnaaf2tm1.1(KOMP)Vlcg | B6N(Cg)-Dnaaf2tm1.1(KOMP)Vlcg/J | J:278736 | View | ||||
primary ciliary dyskinesia 10 | Dnaaf2tm1.1Mkis/Dnaaf2tm1.1Mkis | involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj | J:201474 | View | ||||
primary ciliary dyskinesia 14 | Ccdc39b2b1304Clo/Ccdc39b2b1304Clo | C57BL/6J-Ccdc39b2b1304Clo | J:175213 | View | ||||
primary ciliary dyskinesia 14 | Ccdc39b2b1735Clo/Ccdc39b2b1735Clo | C57BL/6J-Ccdc39b2b1735Clo | J:175213 | View | ||||
primary ciliary dyskinesia 14 | Ccdc39b2b2025.1Clo/Ccdc39b2b2025.1Clo | C57BL/6J-Ccdc39b2b2025.1Clo | J:175213 | View | ||||
primary ciliary dyskinesia 19 | Dnaaf11tm1.2Hmd/Dnaaf11tm1.2Hmd | involves: 129S6/SvEvTac * C57BL/6NCrl | J:258369 | View | ||||
primary ciliary dyskinesia 21 | Drc1b2b1654Clo/Drc1b2b1654Clo | C57BL/6J-Drc1b2b1654Clo | J:175213 | View | ||||
primary ciliary dyskinesia 21 | Drc1b2b2237Clo/Drc1b2b2237Clo | C57BL/6J-Drc1b2b2237Clo | J:175213 | View | ||||
primary ciliary dyskinesia 22 | Zmynd10tm1(KOMP)Wtsi/Zmynd10tm1(KOMP)Wtsi | involves: C57BL/6J * C57BL/6N | J:261915 | View | ||||
primary ciliary dyskinesia 23 | Odad2b2b227.1Clo/Odad2b2b227.1Clo | C57BL/6J-Odad2b2b227.1Clo | J:175213 | View | ||||
primary ciliary dyskinesia 23 | Odad2b2b643Clo/Odad2b2b643Clo | C57BL/6J-Odad2b2b643Clo | J:175213, J:206684 | View | ||||
primary ciliary dyskinesia 25 | Dnaaf4tm1.2Jjlo/Dnaaf4tm1.2Jjlo | involves: 129S1/Sv * 129S4/SvJaeSor * 129S6/SvEvTac * C57BL/6J | J:205312 | View | ||||
primary ciliary dyskinesia 30 | Odad3b2b1885Clo/Odad3b2b1885Clo | C57BL/6J-Odad3b2b1885Clo | J:175213 | View | ||||
primary ciliary dyskinesia 30 | Odad3tm1b(EUCOMM)Hmgu/Odad3tm1b(EUCOMM)Hmgu | C57BL/6N-Odad3tm1b(EUCOMM)Hmgu/Cnrm | J:278798 | View | ||||
primary ciliary dyskinesia 33 | Gas8Gt(CH0760)Wtsi/Gas8em1Bky | involves: 129P2/OlaHsd * C57BL/6 | J:234173 | View | ||||
primary ciliary dyskinesia 33 | Gas8Gt(CH0760)Wtsi/Gas8Gt(CH0760)Wtsi | involves: 129P2/OlaHsd * C57BL/6 | J:234173 | View | ||||
primary ciliary dyskinesia 35 | Odad4em#Omra/Odad4em#Omra | involves: C57BL/6 | J:244361 | View | ||||
primary ovarian insufficiency 12 | Syce1em1Rrca/Syce1em1Rrca | involves: C57BL/6J | J:309952 | View | ||||
primary ovarian insufficiency 13 | Msh5em1Jzc/Msh5em1Jzc | involves: C57BL/6 | J:241778 | View | ||||
primary ovarian insufficiency 19 | Hsf2bpem2Amp/Hsf2bpem2Amp | involves: C57BL/6J * CBA/J | J:303558 | View | ||||
progeria | LmnaDhe/Lmna+ | B6(D2)-LmnaDhe/TyGrsrJ | J:171665 | View | ||||
progeria | Lmnaem1Fenz/Lmna+ | C57BL/6-Lmnaem1Fenz | J:338760 | View | ||||
progeria | Lmnatm1.1Otin/Lmna+ | involves: 129P2/OlaHsd * C57BL/6 | J:211388 | View | ||||
progeria | Lmnatm1.1Otin/Lmna+ | involves: 129P2/OlaHsd * C57BL/6NTac | J:261974 | View | ||||
progeria |
Lmnatm1.1Otin/Lmna+ Nat10tm1a(KOMP)Wtsi/Nat10+ |
involves: 129P2/OlaHsd * C57BL/6NTac | J:261974 | View | ||||
progeria | Lmnatm1.1Otin/Lmnatm1.1Otin | involves: 129P2/OlaHsd * C57BL/6 | J:177575, J:177632, J:211388 | View | ||||
progeria | Lmnatm1.1Otin/Lmnatm1.1Otin | involves: 129P2/OlaHsd * C57BL/6NTac | J:261974 | View | ||||
progeria |
Lmnatm1.1Otin/Lmnatm1.1Otin Nat10tm1a(KOMP)Wtsi/Nat10+ |
involves: 129P2/OlaHsd * C57BL/6NTac | J:261974 | View | ||||
progeria |
Lmnatm1Bliu/Lmna+ Tg(Tek-cre)1Ywa/0 |
involves: C57BL/6 * SJL | J:287256 | View | ||||
progeria | Lmnatm1Lgf/Lmna+ | involves: 129P2/OlaHsd * C57BL/6 | J:113119 | View | ||||
progeria | Lmnatm2Stw/Lmnatm2Stw | involves: 129S1/Sv | J:83382 | View | ||||
progeria | Lmnatm12Lgf/Lmnatm12Lgf | involves: 129P2/OlaHsd * C57BL/6 | J:234711 | View | ||||
progressive familial heart block type IA | Scn5atm1Agrc/Scn5a+ | involves: 129 | J:109689 | View | ||||
progressive familial heart block type IA | Scn5atm1Agrc/Scn5a+ | involves: 129 * C57BL/6J | J:76331 | View | ||||
progressive myoclonus epilepsy 1B | Prickle1em1Yzou/Prickle1+ | C57BL/6-Prickle1em1Yzou | J:321396 | View | ||||
progressive pseudorheumatoid arthropathy of childhood | Ccn6tm1(cre)Mawa/Ccn6tm1(cre)Mawa | involves: 129S4/SvJae * C57BL/6 | J:201718 | View | ||||
progressive pseudorheumatoid arthropathy of childhood | Ccn6tm2Mawa/Ccn6tm2Mawa | 129S/SvEv-Ccn6tm2Mawa | J:94500 | View | ||||
progressive pseudorheumatoid arthropathy of childhood | Ccn6tm2Mawa/Ccn6tm2Mawa | involves: 129S/SvEv * C57BL/6 | J:201718 | View | ||||
proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome | Flvcr2tm1.2Tda/Flvcr2tm1.2Tda | involves: C57BL/6J | J:287134 | View | ||||
pseudoachondroplasia | Comptm1Mbri/Comptm1Mbri | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:125086 | View | ||||
pseudoachondroplasia | Comptm2.1Mbri/Comptm2.1Mbri | involves: 129S1/Sv * 129X1/SvJ | J:206511 | View | ||||
pseudoxanthoma elasticum | Abcc6tm1Aabb/Abcc6tm1Aabb | involves: 129P2/OlaHsd * C57BL/6 | J:105062 | View | ||||
pseudoxanthoma elasticum | Abcc6tm1Jfk/Abcc6tm1Jfk | involves: 129S1/Sv * C57BL/6J | J:101372 | View | ||||
purine nucleoside phosphorylase deficiency | Pnpe/Pnpe | C57BL/6J-Pnpe | J:39328 | View | ||||
purine nucleoside phosphorylase deficiency | Pnpe/Pnpe | involves: C3H/HeHa * C57BL/6J | J:23354 | View | ||||
purine nucleoside phosphorylase deficiency | Pnpf/Pnpf | C57BL/6J-Pnpf | J:39328 | View | ||||
purine nucleoside phosphorylase deficiency | Pnpf/Pnpf | involves: C3H/HeHa * C57BL/6J | J:23354 | View | ||||
purine nucleoside phosphorylase deficiency | Pnpg/Pnpg | involves: C57BL/6 * DBA/2J | J:39328 | View | ||||
pyruvate kinase deficiency of red cells | Pklrchar4/Pklrchar4 | involves: A/J * C57BL/6 | J:86735 | View | ||||
pyruvate kinase deficiency of red cells | Pklrslc/Pklrslc | CBA/NSlc-Pklrslc | J:29199 | View | ||||
renal coloboma syndrome | Pax21Neu/Pax2+ | involves: 102 * CD-1 | J:145105 | View | ||||
renal coloboma syndrome | Pax2M1Bpb/Pax2+ | C57BL/6-Pax2M1Bpb | J:159240 | View | ||||
renal coloboma syndrome | Pax2M1Bpb/Pax2M1Bpb | C57BL/6-Pax2M1Bpb | J:159240 | View | ||||
renal coloboma syndrome | Pax2tm1Pgr/Pax2+ | involves: 129S1/Sv * 129X1/SvJ | J:36834 | View | ||||
renal coloboma syndrome | Pax2tm1Pgr/Pax2tm1Pgr | involves: 129S1/Sv * 129X1/SvJ | J:36834 | View | ||||
renal coloboma syndrome | Pax2tm1Pgr/Pax2tm1Pgr | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:92326 | View | ||||
Renpenning syndrome |
Pqbp1tm1.1Hiok/Y Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * C57BL/6J | J:279053 | View | ||||
retinitis pigmentosa 1 | Rp1m1Jdun/Rp1m1Jdun | C57BL/6-Rp1m1Jdun | J:214837 | View | ||||
retinitis pigmentosa 1 | Rp1tm1Jnz/Rp1tm1Jnz | involves: 129S7/SvEvBrd | J:76071 | View | ||||
retinitis pigmentosa 2 | Rp2Gt(EUCJ0183f04)Hmgu/Rp2Gt(EUCJ0183f04)Hmgu | involves: C57BL/6 * C57BL/6N | J:219642 | View | ||||
retinitis pigmentosa 2 | Rp2Gt(EUCJ0183f04)Hmgu/Y | involves: C57BL/6 * C57BL/6N | J:219642 | View | ||||
retinitis pigmentosa 2 | Rp2tm1.2Asw/Rp2tm1.2Asw | involves: 129S/SvEv * C57BL/6 | J:214194 | View | ||||
retinitis pigmentosa 2 | Rp2tm1.2Asw/Y | involves: 129S/SvEv * C57BL/6 | J:214194 | View | ||||
retinitis pigmentosa 4 | RhoR3/Rho+ | C57BL/6J-RhoR3 | J:153281 | View | ||||
retinitis pigmentosa 4 | RhoR3/RhoR3 | C57BL/6J-RhoR3 | J:153281 | View | ||||
retinitis pigmentosa 4 | RhoR3/Rhotm1Jlem | involves: 129S4/SvJae * C57BL/6J | J:153281 | View | ||||
retinitis pigmentosa 4 | Rhotm1.1Eye/Rho+ | involves: 129S6/SvEvTac * C57BL/6 | J:205477 | View | ||||
retinitis pigmentosa 4 | Rhotm1.1Kpal/Rho+ | involves: 129S6/SvEvTac * C57BL/6 * FVB/N | J:170648 | View | ||||
retinitis pigmentosa 4 |
Rhotm1Jlem/Rhotm1Jlem Tg(RHO*P347S)A1Tili/0 |
involves: 129S4/SvJae * FVB/N | J:280289 | View | ||||
retinitis pigmentosa 4 | Rhotm1Phm/Rhotm1Phm | involves: 129S1/Sv * 129X1/SvJ | J:38098 | View | ||||
retinitis pigmentosa 4 | Rhotm2(RHO/GFP)Jhw/Rhotm2(RHO/GFP)Jhw | involves: 129S7/SvEvBrd | J:128212 | View | ||||
retinitis pigmentosa 4 | Rhotm4.1(RHO*/EGFP)Jhw/Rho+ | B6.129S7-Rhotm4.1(RHO*/EGFP)Jhw | J:196863 | View | ||||
retinitis pigmentosa 4 | RhoTvrm1/Rho+ | C57BL/6J-RhoTvrm1 | J:159523 | View | ||||
retinitis pigmentosa 4 | RhoTvrm4/Rho+ | B6.Cg-RhoTvrm4/Pjn | J:159523 | View | ||||
retinitis pigmentosa 4 | RhoTvrm334/Rho+ | B6.Cg-RhoTvrm334/Pjn | J:243745 | View | ||||
retinitis pigmentosa 4 | Tg(Rho)1Wbae/0 | involves: C57BL/6 * SJL | J:12791 | View | ||||
retinitis pigmentosa 7 | Prph2Rd2/Prph2+ | either: (involves: BALB/c * O20/A) or (involves: GR/A * O20/A) or (involves: O20/A * STS/A) | J:25582 | View | ||||
retinitis pigmentosa 7 | Prph2tm1Nmc/Prph2+ | involves: 129S1/Sv * 129X1/SvJ | J:76490 | View | ||||
retinitis pigmentosa 7 | Prph2tm1Nmc/Prph2tm1Nmc | involves: 129S1/Sv * 129X1/SvJ | J:76490 | View | ||||
retinitis pigmentosa 11 | Prpf31tm1.1Bha/Prpf31+ | involves: 129S2/SvPas | J:171561 | View | ||||
retinitis pigmentosa 12 | Crb1tm1Wij/Crb1tm2Wij | involves: 129P2/OlaHsd * C57BL/6 | J:117415 | View | ||||
retinitis pigmentosa 13 | Prpf8tm1.1Eap/Prpf8+ | involves: 129S6/SvEvTac * C57BL/6 * SJL | J:171561 | View | ||||
retinitis pigmentosa 13 | Prpf8tm1.1Eap/Prpf8tm1.1Eap | involves: 129S6/SvEvTac * C57BL/6 * SJL | J:171561 | View | ||||
retinitis pigmentosa 14 | Tulp1tm1Pjn/Tulp1tm1Pjn | involves: 129X1/SvJ * C57BL/6 | J:59884 | View | ||||
retinitis pigmentosa 18 | Prpf3tm1.1Eap/Prpf3+ | involves: 129S6/SvEvTac * C57BL/6 * SJL | J:171561 | View | ||||
retinitis pigmentosa 18 | Prpf3tm1.1Eap/Prpf3tm1.1Eap | involves: 129S6/SvEvTac * C57BL/6 * SJL | J:171561 | View | ||||
retinitis pigmentosa 19 | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae | J:141801 | View | ||||
retinitis pigmentosa 19 | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae * BALB/c | J:141801 | View | ||||
retinitis pigmentosa 20 | Rpe65tm1Lrcb/Rpe65tm1Lrcb | 129S6/SvEvTac-Rpe65tm1Lrcb | J:130076 | View | ||||
retinitis pigmentosa 26 | Cerklem1Gmar/Cerkltm1.1Geno | involves: 129 * C57BL/6J | J:292626 | View | ||||
retinitis pigmentosa 28 | Fam161aGt(462E7)Cmhd/Fam161aGt(462E7)Cmhd | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:214319 | View | ||||
retinitis pigmentosa 40 | Pde6batrd1/Pde6batrd1 | involves: BALB/cAnN * C3H/HeN | J:101336 | View | ||||
retinitis pigmentosa 40 | Pde6batrd1/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:101336 | View | ||||
retinitis pigmentosa 40 | Pde6batrd1/Pde6btm1Eye | involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cAnN * C3H/HeN * C57BL/6J | J:200898 | View | ||||
retinitis pigmentosa 40 |
Pde6batrd1/Pde6btm1Eye Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+ |
involves: 129S4/SvJae * 129S6/SvEvTac * BALB/cAnN * C3H/HeN * C57BL/6J | J:200898 | View | ||||
retinitis pigmentosa 40 | Pde6batrd2/Pde6batrd2 | involves: BALB/cAnN * C3H/HeN | J:101336 | View | ||||
retinitis pigmentosa 40 | Pde6batrd2/Pde6brd1 | involves: BALB/cAnN * C3H/HeN | J:101336 | View | ||||
retinitis pigmentosa 40 | Pde6batrd3/Pde6batrd3 | involves: BALB/cAnN * C3H/HeN | J:101336 | View | ||||
retinitis pigmentosa 40 | Pde6brd1/Pde6brd1 | C3H/HeJ | J:140115 | View | ||||
retinitis pigmentosa 40 | Pde6brd1/Pde6brd1 | involves: C3H | J:101336 | View | ||||
retinitis pigmentosa 41 | Prom1rd19/Prom1rd19 | B6.BXD83-Prom1rd19/BocJ | J:215591 | View | ||||
retinitis pigmentosa 41 | Prom1tm1Pec/Prom1tm1Pec | B6.129-Prom1tm1Pec | J:146585 | View | ||||
retinitis pigmentosa 56 | Impg2em1Xjz/Impg2em1Xjz | C57BL/6J-Impg2em1Xjz | J:295355 | View | ||||
retinitis pigmentosa 56 | Impg2em2Xjz/Impg2em2Xjz | C57BL/6J-Impg2em2Xjz | J:295355 | View | ||||
retinitis pigmentosa 59 |
Dhddstm1.1Sjpi/Dhddstm1.1Sjpi Tg(BEST1-rtTA,tetO-cre)1Yzl/0 |
involves: C57BL/6J * FVB/N | J:287362 | View | ||||
retinitis pigmentosa 77 | Reep6em1Ruch/Reep6em1Ruch | involves: C57BL/6 | J:248574 | View | ||||
retinitis pigmentosa with or without situs inversus | Arl2bpem1Visu/Arl2bpem1Visu | involves: 129S2/SvPasCrl * C57BL/6J * FVB/N | J:280811 | View | ||||
rhizomelic chondrodysplasia punctata type 1 | Pex7tm1Nbra/Pex7tm1Nbra | involves: 129S/SvEv * C57BL/6 | J:158845 | View | ||||
rhizomelic chondrodysplasia punctata type 1 | Pex7tm1Rjaw/Pex7tm1Rjaw | Swiss | J:92346 | View | ||||
rhizomelic chondrodysplasia punctata type 2 | Gnpattm1Just/Gnpattm1Just | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:84690 | View | ||||
rhizomelic chondrodysplasia punctata type 3 | Agpsbs2/Agpsbs2 | STOCK Agpsbs2/J | J:171265 | View | ||||
RIDDLE syndrome | Rnf168Gt(156B6)Cmhd/Rnf168Gt(156B6)Cmhd | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:198260 | View | ||||
RIDDLE syndrome | Rnf168Gt(405F11)Cmhd/Rnf168Gt(405F11)Cmhd | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:198260 | View | ||||
rigid spine muscular dystrophy 1 | Selenontm1.2Mred/Selenontm1.2Mred | involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL | J:176499 | View | ||||
rippling muscle disease 2 | Cav3tm1Mls/Cav3tm1Mls | involves: 129/Sv * C57BL/6J * SJL | J:69965 | View | ||||
rippling muscle disease 2 | Cav3tm1Ncnp/Cav3tm1Ncnp | involves: 129S4/SvJae * C57BL/10 | J:150127 | View | ||||
rippling muscle disease 2 | Tg(Ckmm-Cav3)1Ysu/0 | involves: C57BL/Slc * DBA/Slc | J:67174 | View | ||||
Rubinstein-Taybi syndrome | CrebbpGt(U-San)112Imeg/Crebbp+ | involves: C57BL/6 * CBA | J:53370 | View | ||||
Rubinstein-Taybi syndrome |
Crebbptm1.2Ltz/Crebbptm1.2Ltz Tg(Camk2a-cre)T29-1Stl/0 |
involves: 129P2/OlaHsd * BALB/c * C57BL * C57BL/6J | J:168984 | View | ||||
Rubinstein-Taybi syndrome | Crebbptm1Dli/Crebbp+ | involves: 129S6/SvEvTac * C57BL/6 | J:60630 | View | ||||
Rubinstein-Taybi syndrome | Crebbptm1Sis/Crebbp+ | involves: C57BL/6NCrlj * CBA/JNCrlj | J:42932 | View | ||||
Saethre-Chotzen syndrome |
Msx2tm1Rilm/Msx2+ Twist1tm1Bhr/Twist1+ |
involves: 129S4/SvJae * 129S7/SvEvBrd * BALB/c * C57BL/6 | J:87044 | View | ||||
Saethre-Chotzen syndrome | Twist1Pas/Twist1+ | involves: C57BL/6 * PDT/Pas | J:86815 | View | ||||
Saethre-Chotzen syndrome | Twist1Pas/Twist1Pas | involves: C57BL/6 * PDT/Pas | J:86815 | View | ||||
Saethre-Chotzen syndrome | Twist1Pde/Twist1+ | involves: 129S1/Sv * C57BL/6J | J:69450 | View | ||||
Saethre-Chotzen syndrome | Twist1Pde/Twist1Pde | involves: 129S1/Sv * C57BL/6J | J:69450 | View | ||||
Saethre-Chotzen syndrome | Twist1tm1Bhr/Twist1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:79294 | View | ||||
Saethre-Chotzen syndrome | Twist1tm1Bhr/Twist1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:44379 | View | ||||
Saethre-Chotzen syndrome | Twist1tm1Bhr/Twist1tm1Bhr | involves: 129S7/SvEvBrd * C57BL/6 | J:44379 | View | ||||
Sandhoff disease |
Ccl3tm1Unc/Ccl3+ Hexbtm1Rlp/Hexbtm1Rlp |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:90687 | View | ||||
Sandhoff disease |
Ccl3tm1Unc/Ccl3tm1Unc Hexbtm1Rlp/Hexbtm1Rlp |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:90687 | View | ||||
Sandhoff disease |
Fcer1gtm1Rav/Fcer1gtm1Rav Hexbtm1Rlp/Hexbtm1Rlp |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:87617 | View | ||||
Sandhoff disease | Hexblysd/Hexblysd | B6.Cg-Hexblysd/J | J:301674 | View | ||||
Sandhoff disease | Hexbtm1Grv/Hexbtm1Grv | either: (involves: 129P2/Ola * C57BL/6J) or (involves: 129S1/Sv * 129X1/SvJ * C57L/6J) | J:30899 | View | ||||
Sandhoff disease | Hexbtm1Rlp/Hexbtm1Rlp | involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:87617 | View | ||||
Sandhoff disease | Hexbtm1Rlp/Hexbtm1Rlp | involves: 129S4/SvJae * C57BL/6 | J:29268, J:190450 | View | ||||
Sandhoff disease |
Hexbtm1Rlp/Hexbtm1Rlp Tg(Hexb-tTA2S,tetO-Hexb)#Tjsa/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:190450 | View | ||||
Sandhoff disease |
Hexbtm1Rlp/Hexbtm1Rlp Tg(SYN1-tTA2S,tetO-Hexb)#Tjsa/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:190450 | View | ||||
scalp-ear-nipple syndrome |
Kctd1tm1c(EUCOMM)Wtsi/Kctd1tm1c(EUCOMM)Wtsi Kctd15tm1c(EUCOMM)Wtsi/Kctd15tm1c(EUCOMM)Wtsi Tg(KRT14-cre)1Amc/0 |
involves: C57BL/6N * C57BL/6NJ | J:344153 | View | ||||
scalp-ear-nipple syndrome |
Kctd1tm1c(EUCOMM)Wtsi/Kctd1tm1c(EUCOMM)Wtsi Tg(Six2-EGFP/cre)1Amc/0 |
involves: C57BL/6J * C57BL/6N * CD-1 | J:344153 | View | ||||
Schimke immuno-osseous dysplasia | Smarcal1tm1.1Cfbo/Smarcal1tm1.1Cfbo | either: B6.129-Smarcal1tm1.1Cfbo or (involves: 129 * C57BL/6) | J:183899 | View | ||||
Schnyder corneal dystrophy | Ubiad1em1Wwk/Ubiad1+ | C57BL/6N-Ubiad1em1Wwk | J:268574 | View | ||||
Schnyder corneal dystrophy | Ubiad1em1Wwk/Ubiad1em1Wwk | C57BL/6N-Ubiad1em1Wwk | J:268574 | View | ||||
Schwartz-Jampel syndrome 1 | Hspg2tm1.1Rdgr/Hspg2tm1.1Rdgr | involves: 129S1/Sv * 129X1/SvJ | J:121855 | View | ||||
Schwartz-Jampel syndrome 1 | Hspg2tm1.1Soni/Hspg2tm1.1Soni | involves: 129S/SvEv * C57BL/6 | J:139975 | View | ||||
Schwartz-Jampel syndrome 1 | Hspg2tm1Nid/Hspg2tm1Nid | involves: 129X1/SvJ * C57BL/6 | J:74542 | View | ||||
Schwartz-Jampel syndrome 1 | Hspg2tm1Rdgr/Hspg2tm1Rdgr | involves: 129S1/Sv * 129X1/SvJ | J:121855 | View | ||||
Schwartz-Jampel syndrome 1 | Hspg2tm1Soni/Hspg2tm1Soni | involves: 129S/SvEv * C57BL/6 | J:139975 | View | ||||
Schwartz-Jampel syndrome 1 | Hspg2tm1Soni/Hspg2tm1Soni | involves: 129S/SvEv * DBA/2J | J:183547 | View | ||||
sclerosteosis 1 | Sosttm1Paz/Sosttm1Paz | involves: 129/Sv * Black Swiss | J:213541 | View | ||||
sclerosteosis 2 | Lrp4mdig-3J/Lrp4mdig-3J | B6.Cg-Lrp4mdig-3J/GrsrJ | J:224655 | View | ||||
sclerosteosis 2 | Lrp4tm1.1Pg/Lrp4tm1.1Pg | involves: C57BL/6N | J:277372 | View | ||||
septooptic dysplasia | Hesx1tm1Icar/Hesx1tm1Icar | involves: 129P2/OlaHsd * C57BL/6 | J:47920, J:60068 | View | ||||
septooptic dysplasia | Hesx1tm2Jpmb/Hesx1tm2Jpmb | involves: 129S/SvEv * C57BL/6J * FVB/N | J:142649 | View | ||||
septooptic dysplasia | Hesx1tm3Jpmb/Hesx1tm3Jpmb | involves: 129S/SvEv * C57BL/6J * FVB/N | J:142649 | View | ||||
severe combined immunodeficiency with sensitivity to ionizing radiation | Dclre1ctm1Jsek/Dclre1ctm1Jsek | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:147864 | View | ||||
severe combined immunodeficiency with sensitivity to ionizing radiation | Dclre1ctm2Mcow/Dclre1ctm2Mcow | involves: 129/Sv * C57BL/6 | J:96535 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive | Rag2tm1Fwa/Rag2tm1Fwa | involves: 129S/SvEv * MF1 | J:1935 | View | ||||
SHORT syndrome | Pik3r1tm1.1Geno/Pik3r1+ | involves: C57BL/6 * C57BL/6J | J:234657 | View | ||||
short-rib thoracic dysplasia 7 with or without polydactyly | Wdr35yeti/Wdr35yeti | Not Specified | J:171617 | View | ||||
short-rib thoracic dysplasia 9 with or without polydactyly | Ift140b2b1283Clo/Ift140b2b1283Clo | C57BL/6J-Ift140b2b1283Clo | J:175213 | View | ||||
Silverman-Handmaker type dyssegmental dysplasia | Hspg2tm1Nid/Hspg2tm1Nid | involves: 129X1/SvJ * C57BL/6 | J:74542 | View | ||||
Silverman-Handmaker type dyssegmental dysplasia | Hspg2tm1Ref/Hspg2tm1Ref | involves: 129S1/Sv * 129X1/SvJ | J:84739 | View | ||||
Simpson-Golabi-Behmel syndrome type 1 | Gpc3Gt(Ex136)Byg/Gpc3+ | involves: 129P2/OlaHsd * C57BL/6 | J:64330 | View | ||||
Simpson-Golabi-Behmel syndrome type 1 | Gpc3Gt(Ex136)Byg/Y | involves: 129P2/OlaHsd * C57BL/6 | J:64330 | View | ||||
Simpson-Golabi-Behmel syndrome type 1 | Gpc3tm1Arge/Y | either: (involves: 129S/SvEv * 129S1/Sv) or (involves: 129S1/Sv * C57BL/6J) | J:75054 | View | ||||
Simpson-Golabi-Behmel syndrome type 1 |
Gpc3tm1Arge/Y H19tm1Tilg/H19+ |
involves: 129S/SvEv * 129S1/Sv | J:75054 | View | ||||
Simpson-Golabi-Behmel syndrome type 1 | Gpc3tm1Fil/Gpc3+ | B6.Cg-Gpc3tm1Fil | J:73877 | View | ||||
Simpson-Golabi-Behmel syndrome type 1 | Gpc3tm1Fil/Y | B6.Cg-Gpc3tm1Fil | J:73877 | View | ||||
Simpson-Golabi-Behmel syndrome type 1 | Gpc3tm1Snd/Gpc3+ | involves: 129X1/SvJ * C57BL/6 | J:64330 | View | ||||
Simpson-Golabi-Behmel syndrome type 1 | Gpc3tm1Snd/Y | involves: 129X1/SvJ * C57BL/6 | J:64330 | View | ||||
sitosterolemia | Abcg8tm1Elk/Abcg8tm1Elk | involves: 129S6/SvEvTac * C57BL/6J | J:94759 | View | ||||
Smith-McCort dysplasia 2 | Rab33bem1Rmr/Rab33b+ | involves: C57BL/6 | J:338833 | View | ||||
Smith-McCort dysplasia 2 | Rab33bem1Rmr/Rab33bem1Rmr | involves: C57BL/6 | J:338833 | View | ||||
Sorsby's fundus dystrophy | Timp3tm1Web/Timp3+ | either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) | J:78059 | View | ||||
Sorsby's fundus dystrophy | Timp3tm1Web/Timp3tm1Web | either: (involves: 129/Sv) or (involves: 129/Sv * C57BL/6) | J:78059 | View | ||||
Sotos syndrome 2 | Nfixtm1.1Rmg/Nfix+ | involves: 129S4/SvJae * C57BL/6J | J:295051 | View | ||||
spastic tetraplegia, thin corpus callosum, and progressive microcephaly | Slc1a4em2Tmg/Slc1a4em2Tmg | involves: C57BL/6J | J:344184 | View | ||||
spermatogenic failure 19 | Cfap43em1Fzh/Cfap43em1Fzh | involves: C57BL/6 | J:258613 | View | ||||
spermatogenic failure 19 | Cfap43em2Fzh/Cfap43em2Fzh | involves: C57BL/6 | J:258613 | View | ||||
spermatogenic failure 20 | Cfap44em1Fzh/Cfap44em1Fzh | involves: C57BL/6 | J:258613 | View | ||||
spermatogenic failure 24 | Cfap69em1Fzh/Cfap69em1Fzh | involves: C57BL/6J | J:288345 | View | ||||
spermatogenic failure 24 | Cfap69tm1b(KOMP)Wtsi/Cfap69tm1b(KOMP)Wtsi | involves: C57BL/6N | J:263440 | View | ||||
spermatogenic failure 31 | Pmfbp1em#Jfw/Pmfbp1em#Jfw | Not Specified | J:303070 | View | ||||
spermatogenic failure 39 | Dnah17em1Qsh/Dnah17em1Qsh | involves: C57BL/6 * DBA/2J | J:285088 | View | ||||
spermatogenic failure 40 | Cfap65em1Fzh/Cfap65em1Fzh | involves: C57BL/6 | J:292578 | View | ||||
spermatogenic failure 46 | Dnah8em1Osb/Dnah8em1Osb | involves: C57BL/6 * DBA/2 | J:297137 | View | ||||
spermatogenic failure 47 | Dzip1em1Yxc/Dzip1em1Yxc | Not Specified | J:333286 | View | ||||
spinocerebellar ataxia type 1 | Atxn1tm1Hzo/Atxn1+ | involves: 129S7/SvEvBrd * C57BL/6 | J:77225 | View | ||||
spinocerebellar ataxia type 2 | Atxn2tm2.1Aub/Atxn2tm2.1Aub | B6.129S2-Atxn2tm2.1Aub | J:188118 | View | ||||
spinocerebellar ataxia type 5 | Sptbn2Gt(XK442)Byg/Sptbn2Gt(XK442)Byg | involves: 129P2/OlaHsd * C57BL/6J | J:158494 | View | ||||
spinocerebellar ataxia type 5 | Sptbn2tm1Mjac/Sptbn2tm1Mjac | B6.129P2-Sptbn2tm1Mjac | J:159622 | View | ||||
spinocerebellar ataxia type 6 | Cacna1asmrl/Cacna1asmrl | CXB10/HiAJ-Cacna1asmrl/GrsrJ | J:222308 | View | ||||
spinocerebellar ataxia type 6 | Cacna1atm2.1Kewa/Cacna1atm2.1Kewa | B6.Cg-Cacna1atm2.1Kewa | J:190729 | View | ||||
spinocerebellar ataxia type 6 | Cacna1atm3Hzo/Cacna1atm3Hzo | B6.129S7-Cacna1atm3Hzo/J | J:239981 | View | ||||
spinocerebellar ataxia type 7 | Atxn7tm1Hzo/Atxn7+ | involves: 129S7/SvEvBrd | J:113150, J:179021 | View | ||||
spinocerebellar ataxia type 7 | Atxn7tm1Hzo/Atxn7+ | involves: 129S7/SvEvBrd * C57BL/6 | J:82072 | View | ||||
spinocerebellar ataxia type 7 | Atxn7tm1Hzo/Atxn7+ | involves: 129S7/SvEvBrd * C57BL/6J | J:107098 | View | ||||
spinocerebellar ataxia type 7 | Atxn7tm1Hzo/Atxn7tm1Hzo | involves: 129S7/SvEvBrd | J:179021 | View | ||||
spinocerebellar ataxia type 7 |
Atxn7tm1Hzo/Atxn7tm1Hzo Kat2atm3.1Roth/Kat2a+ |
involves: 129 * 129S7/SvEvBrd | J:179021 | View | ||||
spinocerebellar ataxia type 14 | Prkcgem1Jpka/Prkcg+ | FVB/N-Prkcgem1Jpka | J:305637 | View | ||||
spinocerebellar ataxia type 14 | Prkcgem1Jpka/Prkcgem1Jpka | FVB/N-Prkcgem1Jpka | J:305637 | View | ||||
spinocerebellar ataxia type 17 |
Tbptm1Xjl/Tbp+ Tg(CAG-cre/Esr1*)5Amc/0 |
involves: 129S/SvEv * C57BL/6 * CBA | J:213011 | View | ||||
spinocerebellar ataxia type 28 | Afg3l2Emv66/Afg3l2+ | involves: MEV/2Ty | J:151797 | View | ||||
spinocerebellar ataxia with axonal neuropathy 1 | Tdp1Gt(XD105)Byg/Tdp1Gt(XD105)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:127605 | View | ||||
split hand-foot malformation 1 | Del(6Dlx6-Dlx5)1Tlu/Del(6Dlx6-Dlx5)1Tlu | Not Specified | J:76480 | View | ||||
split hand-foot malformation 1 | Dlx5/Dlx6tm1Levi/Dlx5/Dlx6tm1Levi | Not Specified | J:77244 | View | ||||
spondylocarpotarsal synostosis syndrome | FlnbGt(RRF239)Byg/FlnbGt(RRF239)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:132026 | View | ||||
spondylocarpotarsal synostosis syndrome | FlnbGt(XD076)Byg/FlnbGt(XD076)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:134094 | View | ||||
spondyloepimetaphyseal dysplasia, Pakistani type | Papss2bm/Papss2bm | LDJ/Le | J:5109 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1Lpk/Col2a1+ | C.B6(C3)-Col2a1Lpk | J:187141 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1Lpk/Col2a1+ | involves: C3H/HeH * C57BL/6J | J:187141 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1M2J/Col2a1+ | B6;C3Fe-Col2a1M2J/GrsrJ | J:222308 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1M3J/Col2a1+ | B6(Cg)-Col2a1M3J/GrsrJ | J:222308 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1sedc/Col2a1sedc | involves: C57BL/6J | J:85735 | View | ||||
spondyloepiphyseal dysplasia congenita | Col2a1tm1Prc/Col2a1tm1Prc | involves: 129/Sv * C57BL/6 | J:30041 | View | ||||
spondyloepiphyseal dysplasia congenita | Tg(Col2a1*R789C)#Waho/0 | involves: C57BL/6 * DBA/2 | J:112540 | View | ||||
STING-associated vasculopathy with onset in infancy | Sting1em1Jmin/Sting1+ | involves: C57BL/6N | J:251372 | View | ||||
Stormorken syndrome | Stim1tm3Ics/Stim1+ | involves: C57BL/6N | J:277842, J:327797 | View | ||||
syndromic microphthalmia 2 |
Bcortm1.1Vjba/Bcor+ Tmem163Tg(ACTB-cre)2Mrt/Tmem163+ |
involves: 129S1/Sv * C57BL/6N * FVB/N | J:296645 | View | ||||
syndromic X-linked intellectual developmental disorder bain type | Hnrnph2em1Jpat/Hnrnph2+ | C57BL/6J-Hnrnph2em1Jpat | J:338313 | View | ||||
syndromic X-linked intellectual developmental disorder bain type | Hnrnph2em1Jpat/Y | C57BL/6J-Hnrnph2em1Jpat | J:338313 | View | ||||
syndromic X-linked intellectual developmental disorder bain type | Hnrnph2em2Jpat/Y | C57BL/6J-Hnrnph2em2Jpat | J:338313 | View | ||||
syndromic X-linked intellectual disability 5 | Ap1s2tm1Pschu/Ap1s2tm1Pschu | involves: 129P2/OlaHsd * C57BL/6 | J:218588 | View | ||||
syndromic X-linked intellectual disability Claes-Jensen type | Kdm5ctm1.2Yshi/Y | involves: 129 * 129S1/SvImJ * C57BL/6J | J:262206 | View | ||||
syndromic X-linked intellectual disability Raymond type | Zdhhc9tm1Lex/Y | B6.129S5-Zdhhc9tm1Lex | J:268248 | View | ||||
syndromic X-linked intellectual disability Siderius type | Phf8tm1.1Cdcn/Y | B6.129S6(Cg)-Phf8tm1.1Cdcn | J:258245 | View | ||||
T-cell immunodeficiency, congenital alopecia, and nail dystrophy | Foxn1nu-2J/Foxn1nu-2J | B6(SJL)-Foxn1nu-2J/GrsrJ | J:222308 | View | ||||
T-cell immunodeficiency, congenital alopecia, and nail dystrophy | Foxn1nu-Y/Foxn1nu-Y | 101/HY-Foxn1nu-Y | J:29022 | View | ||||
T-cell immunodeficiency, congenital alopecia, and nail dystrophy | Foxn1nu/Foxn1nu | Not Specified | J:11959 | View | ||||
T-cell immunodeficiency, congenital alopecia, and nail dystrophy | Foxn1tm1Tbo/Foxn1tm1Tbo | involves: 129S1/Sv | J:33796 | View | ||||
Tay-Sachs disease | Hexatm1Cota/Hexatm1Cota | involves: 129S2/SvPas * C57BL/6 | J:30435 | View | ||||
Tay-Sachs disease | Hexatm1Grv/Hexatm1Grv | involves: 129P2/Ola * C57BL/6J | J:30899 | View | ||||
Tay-Sachs disease | Hexatm1Rlp/Hexatm1Rlp | involves: 129S4/SvJae * C57BL/6 | J:21008 | View | ||||
Teebi hypertelorism syndrome 1 | Specc1lem3Kumc/Specc1lem3Kumc | involves: C57BL/6J * FVB/NJ | J:324294 | View | ||||
Teebi hypertelorism syndrome 1 | Specc1lem4Kumc/Specc1lem4Kumc | involves: C57BL/6J * FVB/NJ | J:324294 | View | ||||
thiamine-responsive megaloblastic anemia syndrome | Slc19a2tm1Ejn/Slc19a2tm1Ejn | involves: 129S4/SvJae * 129S6/SvEvTac | J:101675 | View | ||||
thiamine-responsive megaloblastic anemia syndrome | Slc19a2tm1Gelb/Slc19a2tm1Gelb | involves: 129X1/SvJ | J:79974 | View | ||||
tibial muscular dystrophy | Ttntm1.1Isrd/Ttn+ | involves: 129S2/SvPas * C57BL/6 | J:165576 | View | ||||
Tietz syndrome | MitfMi-Crc/Mitf+ | involves: CBA/CaCrc | J:83500 | View | ||||
Tietz syndrome | MitfMi-Crc/MitfMi-Crc | involves: CBA/CaCrc | J:83500 | View | ||||
Tietz syndrome | Mitfmi-enu122/Mitf+ | involves: 102 * C3H | J:46254 | View | ||||
Tietz syndrome | Mitfmi-enu122/Mitfmi-enu122 | involves: 102 * C3H | J:46254 | View | ||||
Tietz syndrome | MitfMi-H/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Tietz syndrome | MitfMi-H/MitfMi-H | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Tietz syndrome | MitfMi-H/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Tietz syndrome | MitfMi-wh/Mitf+ | involves: C57BL * DBA | J:13058 | View | ||||
Tietz syndrome | MitfMi-wh/MitfMi-wh | involves: C57BL * DBA | J:13058 | View | ||||
Tietz syndrome | MitfMi-wh/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
Tietz syndrome | Mitfmi-x/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
Tietz syndrome | MitfMi/MitfMi | Not Specified | J:30758 | View | ||||
Tietz syndrome | MitfRorp/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Tietz syndrome | MitfRorp/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Timothy syndrome | Cacna1ctm2Itl/Cacna1c+ | involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac | J:176442 | View | ||||
torsion dystonia 1 | Tor1atm1Wtd/Tor1a+ | B6;129-Tor1atm1Wtd/J | J:225496 | View | ||||
torsion dystonia 1 | Tor1atm1Yql/Tor1a+ | involves: 129S2/SvPas * C57BL/6 | J:104513 | View | ||||
torsion dystonia 1 | Tor1atm2Wtd/Tor1a+ | B6.129S1-Tor1atm2Wtd | J:171370, J:201962 | View | ||||
torsion dystonia 1 | Tor1atm2Wtd/Tor1a+ | involves: 129S1/Sv | J:201535 | View | ||||
torsion dystonia 6 | Thap1tm1.1Meeh/Thap1+ | involves: 129S/SvEv * C3H * C57BL/6 | J:226849 | View | ||||
torsion dystonia 6 | Thap1tm1.2Meeh/Thap1+ | involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6 | J:226849 | View | ||||
Townes-Brocks syndrome | Sall1tm1.1Mrau/Sall1+ | involves: 129X1/SvJ | J:161758 | View | ||||
Townes-Brocks syndrome | Sall1tm1Mrau/Sall1+ | involves: 129X1/SvJ * ICR | J:85458 | View | ||||
Townes-Brocks syndrome | Sall1tm1Mrau/Sall1tm1Mrau | involves: 129X1/SvJ * ICR | J:85458 | View | ||||
transthyretin amyloidosis |
Rbp4tm1(RBP4)Zhel/Rbp4tm1(RBP4)Zhel Ttrtm2(TTR)Kymm/Ttrtm2(TTR)Kymm |
B6.Cg-Ttrtm2(TTR)Kymm Rbp4tm1(RBP4)Zhel | J:260683 | View | ||||
transthyretin amyloidosis |
Rbp4tm1(RBP4)Zhel/Rbp4tm1(RBP4)Zhel Ttrtm2(TTR)Kymm/Ttrtm3(TTR*)Kymm |
Not Specified | J:260683 | View | ||||
transthyretin amyloidosis | Tg(TTR)#Jbux/0 | involves: C57BL/6 * DBA/2 | J:68458 | View | ||||
transthyretin amyloidosis | Ttrtm1.1Smoc/? | involves: C57BL/6J * C57BL/6N | J:257096 | View | ||||
Treacher Collins syndrome | Tcof1tm1Mjd/Tcof1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:62928 | View | ||||
Treacher Collins syndrome | Tcof1tm1Mjd/Tcof1+ | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * DBA/1 | J:112900 | View | ||||
trichorhinophalangeal syndrome type I | Trps1tm1.1Shiv/Trps1+ | either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * BALB/c) or (involves: 129S4/SvJae * C57BL/6) | J:80615 | View | ||||
Troyer syndrome | Sparttm1.1Xen/Sparttm1.1Xen | involves: C57BL/6J | J:185987 | View | ||||
tuberous sclerosis |
Myl2tm1(cre)Krc/Myl2+ Tsc1tm1Djk/Tsc1tm1Djk |
involves: 129S4/SvJae | J:96138 | View | ||||
tuberous sclerosis | Tg(CMV-Tsc2*)1Arbi/0 | involves: C57BL/6 | J:96943, J:179850 | View | ||||
tuberous sclerosis |
Tg(GFAP-cre)8Gtm/0 Tsc2tm1.1Mjg/Tsc2tm1.1Mjg |
involves: 129X1/SvJ * 129S1/Sv * C57BL/6 * CBA | J:167241 | View | ||||
tuberous sclerosis |
Tg(Pcp2-cre)2Mpin/0 Tsc2tm1.1Mjg/Tsc2tm1.1Mjg |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:174327 | View | ||||
tuberous sclerosis |
Tg(Pcp2-cre)2Mpin/0 Tsc2tm1.1Mjg/Tsc2tm1.2Mjg |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:174327 | View | ||||
tuberous sclerosis | Tsc1tm1.1Djk/Tsc1+ | either: 129S4/SvJae-Tsc1tm1Djk or (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * C57BL/6J) | J:75243 | View | ||||
tuberous sclerosis | Tsc1tm1Chdl/Tsc1+ | involves: 129P2/OlaHsd * Balb/cOlaHsd * C57BL/6JOlaHsd | J:99796 | View | ||||
tuberous sclerosis | Tsc1tm1Chdl/Tsc1+ | involves: 129P2/OlaHsd * C3H/HeNHsd * C57BL/6JOlaHsd | J:99796 | View | ||||
tuberous sclerosis | Tsc1tm1Chdl/Tsc1+ | involves: 129P2/OlaHsd * C57BL/6JOlaHsd | J:99796 | View | ||||
tuberous sclerosis |
Tsc1tm1Djk/Tsc1tm1.1Djk Tg(Syn1-cre)671Jxm/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:136366 | View | ||||
tuberous sclerosis |
Tsc1tm1Djk/Tsc1tm1Djk Gt(ROSA)26Sortm1Sho/Gt(ROSA)26Sor+ |
involves: 129S4/SvJae * 129S4/SvJaeSor | J:221022 | View | ||||
tuberous sclerosis |
Tsc1tm1Djk/Tsc1tm1Djk Tg(GFAP-cre)8Gtm/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:134889, J:167241 | View | ||||
tuberous sclerosis | Tsc1tm1Hin/Tsc1+ | B6J.129S4-Tsc1tm1Hin | J:221239 | View | ||||
tuberous sclerosis | Tsc1tm1Hin/Tsc1+ | involves: 129S4/SvJae * C57BL/6J | J:70463 | View | ||||
tuberous sclerosis | Tsc2tm1Djk/Tsc2+ | either: (involves: 129S4/SvJae * BALB/cJ) or (involves: 129S4/SvJae * Black Swiss) or (involves: 129S4/SvJae * C57BL/6J) | J:57631 | View | ||||
tuberous sclerosis | Tsc2tm1Djk/Tsc2+ | involves: 129S4/SvJae * C57BL/6NCrl | J:138621 | View | ||||
tuberous sclerosis | Tsc2tm1Tno/Tsc2+ | B6J.129S4-Tsc2tm1Tno | J:221239 | View | ||||
tuberous sclerosis | Tsc2tm1Tno/Tsc2+ | involves: 129S4/SvJae * C57BL/6J | J:52464 | View | ||||
tuberous sclerosis | Tsc2tm2.2Djk/Tsc2+ | involves: 129S4/SvJae * C57BL/6 | J:149326 | View | ||||
tubular aggregate myopathy 1 | Stim1tm1.1Pg/Stim1+ | involves: C57BL/6 | J:285187 | View | ||||
tubular aggregate myopathy 1 | Stim1tm3Ics/Stim1+ | involves: C57BL/6N | J:277842, J:327797 | View | ||||
Ullrich congenital muscular dystrophy | Col6a1tm1Sngi/Col6a1tm1Sngi | B6.Cg-Col6a1tm1Sngi | J:278926 | View | ||||
Ullrich congenital muscular dystrophy | Col6a3tm2.1Chu/Col6a3+ | B6.129(Cg)-Col6a3tm2.1Chu | J:208903 | View | ||||
ulnar-mammary syndrome | Tbx3tm1Pa/Tbx3tm1Pa | either: (involves: 129 * 129S1/Sv * 129X1/SvJ) or (involves: 129 * 129S1/Sv * 129X1/SvJ * C57BL/6NTac) | J:82458 | View | ||||
urofacial syndrome | Hpse2Gt(OST411605)Lex/Hpse2Gt(OST411605)Lex | involves: 129S5/SvEvBrd * C57BL/6 | J:219597 | View | ||||
Usher syndrome type 1 | Myo7a26SB/Myo7a26SB | involves: BALB/cRl | J:42644 | View | ||||
Usher syndrome type 1 | Myo7a816SB/Myo7a816SB | involves: BALB/cRl | J:42644 | View | ||||
Usher syndrome type 1 | Myo7a816SB/Myo7a816SB | involves: BALB/cRl * 47BS/Rl | J:46373 | View | ||||
Usher syndrome type 1 | Myo7a3336SB/Myo7a3336SB | involves: BALB/cRl | J:42644 | View | ||||
Usher syndrome type 1 | Myo7a4494SB/Myo7a4494SB | involves: BALB/cRl | J:42644 | View | ||||
Usher syndrome type 1 | Myo7aHdb/Myo7a4626SB | involves: BALB/c * 47BS/Rl * C3HeB/FeJ * CBA/Ca | J:93998 | View | ||||
Usher syndrome type 1 | Myo7apolka/Myo7apolka | involves: C57BL/6J | J:157102 | View | ||||
Usher syndrome type 1 | Myo7ash1-6J/Myo7ash1-6J | involves: C57BLKS/J | J:17340 | View | ||||
Usher syndrome type 1 | Myo7ash1-9J/Myo7ash1-9J | involves: C3.MRL-Faslpr/J | J:49039 | View | ||||
Usher syndrome type 1 | Myo7ash1-11J/Myo7ash1-11J | 129.B6-Myo7ash1-11J | J:181430 | View | ||||
Usher syndrome type 1 | Myo7ash1-13J/Myo7ash1-13J | C.Cg-Myo7ash1-13J/GrsrJ | J:222308 | View | ||||
Usher syndrome type 1 | Myo7ash1/Myo7ash1 | involves: BALB | J:15554, J:5133 | View | ||||
Usher syndrome type 1 | Myo7atm1b(EUCOMM)Wtsi/Myo7atm1b(EUCOMM)Wtsi | B6J.Cg-Myo7atm1b(EUCOMM)Wtsi | J:283233 | View | ||||
Usher syndrome type 1C | Ush1cdfcr-2J/Ush1cdfcr-2J | B6;129S4 | J:85400 | View | ||||
Usher syndrome type 1C | Ush1cdfcr-3J/Ush1cdfcr-3J | STOCK Ush1cdfcr-3J/J | J:147859 | View | ||||
Usher syndrome type 1C | Ush1cdfcr-4J/Ush1cdfcr-4J | 129P3/J-Ush1cdfcr-4J/J | J:278662 | View | ||||
Usher syndrome type 1C | Ush1cdfcr/Ush1cdfcr | involves: BALB/cByJ | J:85400 | View | ||||
Usher syndrome type 1C | Ush1ctm1Bkts/Ush1ctm1Bkts | involves: 129S6/SvEvTac * C57BL/6J * FVB/N | J:118248 | View | ||||
Usher syndrome type 1C | Ush1ctm1Xzl/Ush1ctm1Xzl | involves: 129S1/Sv * 129X1/SvJ | J:212327 | View | ||||
Usher syndrome type 1D | Cdh23v-2J/Cdh23v-2J | B6(V)-Cdh23v-2J/J | J:66698 | View | ||||
Usher syndrome type 1D | Cdh23v-3J/Cdh23+ | C57BL/6J-Cdh23v-3J | J:174130 | View | ||||
Usher syndrome type 1D | Cdh23v-4J/Cdh23v-4J | involves: C57BLKS/J | J:174130 | View | ||||
Usher syndrome type 1D | Cdh23v-5J/Cdh23v-5J | involves: SENCARA/PtJ | J:174130 | View | ||||
Usher syndrome type 1D | Cdh23v-6J/Cdh23v-6J | B10.A-H2h4/(4R)SgDvEgJ-Cdh23v-6J/J | J:66698 | View | ||||
Usher syndrome type 1D | Cdh23v-7J/Cdh23v-7J | CByJ(Cg)-Cdh23v-7J/GrsrJ | J:174130 | View | ||||
Usher syndrome type 1D | Cdh23v-Alb/Cdh23v-Alb | involves: C3H/HeJ * C57BL/6 | J:66698 | View | ||||
Usher syndrome type 1D | Cdh23v-bus/Cdh23v-bus | involves: KYF/MsIdr | J:174130 | View | ||||
Usher syndrome type 1D | Cdh23v-J/Cdh23v-J | B6.C-H2-Kbm1/ByJ | J:174130 | View | ||||
Usher syndrome type 1D | Cdh23v-ngt/Cdh23v-ngt | involves: ICR * MSM | J:174130 | View | ||||
Usher syndrome type 1D | Cdh23v/Cdh23v | involves: fancier's stocks | J:174130 | View | ||||
Usher syndrome type 1F | Pcdh15av-3J/Pcdh15av-3J | C57BL/6J-Pcdh15av-3J/J | J:95655 | View | ||||
Usher syndrome type 1F | Pcdh15av-Jfb/Pcdh15av-Jfb | involves: 129X1/SvJ * C57BL/6 | J:84779 | View | ||||
Usher syndrome type 1F | Pcdh15roda/Pcdh15roda | BALB/c-Pcdh15roda | J:220658 | View | ||||
Usher syndrome type 1G | Ush1gjs-2J/Ush1gjs-2J | B6(Cg)-Ush1gjs-2J/J | J:112552 | View | ||||
Usher syndrome type 1G | Ush1gjs-3J/Ush1gjs-3J | B6.Cg-Ush1gjs-3J/Kjn | J:184204 | View | ||||
Usher syndrome type 1G | Ush1gjs/Ush1gjs | B6.A-Ush1gjs/J | J:82022 | View | ||||
Usher syndrome type 2A | Ush2atm1Tili/Ush2atm1Tili | involves: 129S4/SvJae * C57BL/6 | J:118927 | View | ||||
Usher syndrome type 2C | Adgrv1m1/Adgrv1m1 | CBACa.KM-Adgrv1m1 | J:273686 | View | ||||
Usher syndrome type 2C | Adgrv1tm1Msat/Adgrv1tm1Msat | involves: 129P2/OlaHsd * C57BL/6J | J:122415 | View | ||||
Usher syndrome type 2C | Adgrv1tm1Pwh/Adgrv1tm1Pwh | involves: 129S1/Sv * C57BL/6J | J:109595 | View | ||||
Usher syndrome type 2D |
Rpe65450L/Rpe65450L Whrnwi/Whrnwi |
129.Cg(B6)-Whrnwi | J:210386 | View | ||||
Usher syndrome type 2D | Whrntm1Tili/Whrntm1Tili | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:160677 | View | ||||
Usher syndrome type 3A | Clrn1tm1.1Kuna/Clrn1tm1.1Kuna | involves: C57BL/6J | J:150215 | View | ||||
Usher syndrome type 3A |
Clrn1tm1.1Ugpa/Clrn1tm1.1Ugpa Myo15atm1.1(cre)Ugds/Myo15a+ |
involves: 129S1/SvImJ * C57BL/6N | J:265318 | View | ||||
Usher syndrome type 3A | Clrn1tm2.1Kuna/Clrn1tm2.1Kuna | involves: 129 * BALB/cJ * C57BL/6J | J:186316 | View | ||||
vascular type Ehlers-Danlos syndrome | Col3a1m1Lsmi/Col3a1+ | involves: 129P2/OlaHsd * C57BL/6J | J:180733 | View | ||||
vascular type Ehlers-Danlos syndrome | Col3a1tm1Jae/Col3a1tm1Jae | involves: 129S4/SvJae | J:39273 | View | ||||
vestibular schwannomatosis |
Nf2tm2Gth/Nf2tm2Gth Tg(Postn-cre)1Sjc/0 |
involves: 129P2/OlaHsd * FVB/NTac | J:216420 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-1Wli/Pax3+ | involves: C57BL/6J * CBA/CaJ | J:196572 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-2H/Pax3+ | involves: C57BL/6 | J:14096 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-2H/Pax3Sp-2H | involves: 101 * C3H/He * CBA/Ca | J:46341 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-2H/Pax3Sp-2H | involves: C57BL/6 | J:14096 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-d/Pax3+ | C57BL/6J-Pax3Sp-d | J:238 | View | ||||
Waardenburg syndrome type 1 | Pax3Sp-d/Pax3Sp-d | C57BL/6J-Pax3Sp-d | J:238, J:70476 | View | ||||
Waardenburg syndrome type 2A |
Mitfmi-bw/Mitfmi-bw Tg(Dct-lacZ)A12Jkn/0 |
involves: C3H * C57BL/6 * C57BL/6J * CBA | J:213982 | View | ||||
Waardenburg syndrome type 2A | MitfMi-Crc/MitfMi-Crc | involves: CBA/CaCrc | J:83500 | View | ||||
Waardenburg syndrome type 2A | Mitfmi-enu122/Mitf+ | involves: 102 * C3H | J:46254 | View | ||||
Waardenburg syndrome type 2A | Mitfmi-enu122/Mitfmi-enu122 | involves: 102 * C3H | J:46254 | View | ||||
Waardenburg syndrome type 2A | MitfMi-H/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 2A | MitfMi-H/MitfMi-H | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 2A | MitfMi-H/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 2A | MitfMi-wh/Mitf+ | involves: C57BL * DBA | J:13058 | View | ||||
Waardenburg syndrome type 2A | MitfMi-wh/MitfMi-wh | involves: C57BL * DBA | J:13058 | View | ||||
Waardenburg syndrome type 2A | MitfMi-wh/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
Waardenburg syndrome type 2A | Mitfmi-x/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
Waardenburg syndrome type 2A | MitfMi/MitfMi | Not Specified | J:30758 | View | ||||
Waardenburg syndrome type 2A | MitfRorp/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 2A | MitfRorp/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
Waardenburg syndrome type 4A | Ednrbtm1Ywa/Ednrbtm1Ywa | involves: 129S5/SvEvBrd | J:93622 | View | ||||
Waardenburg syndrome type 4A | EdnrbWS4/EdnrbWS4 | involves: BALB/c * MSM | J:76584 | View | ||||
Waardenburg syndrome type 4B | Edn3tm1Ywa/Edn3tm1Ywa | involves: 129S7/SvEvBrd | J:22207 | View | ||||
Waardenburg syndrome type 4B | Edn3tmgc48/Edn3+ | C57BL/6-19PWK | J:137432 | View | ||||
Waardenburg syndrome type 4B | Edn3tmgc48/Edn3tmgc48 | C57BL/6-19PWK | J:137432 | View | ||||
Waardenburg syndrome type 4C | Sox10Dom/Sox10+ | C57BL/6J-Sox10Dom | J:165146 | View | ||||
Walker-Warburg syndrome | Pomgnt1Gt(OST179231)Lex/Pomgnt1Gt(OST179231)Lex | involves: 129S5/SvEvBrd * C57BL/6J | J:107697, J:196379 | View | ||||
Walker-Warburg syndrome | Pomgnt1tm1Stk/Pomgnt1tm1Stk | involves: 129S/SvEv | J:144928 | View | ||||
Warburg micro syndrome 3 | Rab18Gt(EUCE0233a03)Hmgu/Rab18Gt(EUCE0233a03)Hmgu | involves: 129P2/OlaHsd * C57BL/6J | J:211808 | View | ||||
Warburg micro syndrome 3 | Rab18m1Hongc/Rab18m1Hongc | C57BL/6J-Rab18m1Hongc | J:220974 | View | ||||
Warburg micro syndrome 4 | Tbc1d20bs/Tbc1d20bs | 129S;AKR-Tbc1d20bs/J | J:206668 | View | ||||
Warburg micro syndrome 4 | Tbc1d20em1Djsi/Tbc1d20em1Djsi | involves: C57BL/6 * DBA/2 | J:315009 | View | ||||
Weaver syndrome | Ezh2em1Jbn/Ezh2+ | C57BL/6J-Ezh2em1Jbn | J:267184 | View | ||||
Weaver syndrome | Ezh2em1Jbn/Ezh2em1Jbn | C57BL/6J-Ezh2em1Jbn | J:267184 | View | ||||
Weaver syndrome | Ezh2em1Jiaf/Ezh2+ | C57BL/6J-Ezh2em1Jiaf | J:345603 | View | ||||
Weill-Marchesani syndrome | Adamts10em1Cbal/Adamts10em1Cbal | involves: C57BL/6 * C57BL/6J * DBA/2 | J:266801 | View | ||||
Weill-Marchesani syndrome | Adamts10em1Jku/Adamts10em1Jku | C57BL/6J-Adamts10em1Jku | J:311879 | View | ||||
Weill-Marchesani syndrome | Adamts17tm1.2Taks/Adamts17tm1.2Taks | involves: C57BL * C57BL/6 * DBA | J:295274 | View | ||||
Weill-Marchesani syndrome | Fbn1tm3.2Lysa/Fbn1+ | Not Specified | J:181493 | View | ||||
Weill-Marchesani syndrome | Fbn1tm3.2Lysa/Fbn1tm3.2Lysa | Not Specified | J:181493 | View | ||||
Werner syndrome |
Terctm1Rdp/Terctm1Rdp Wrntm1Lgu/Wrntm1Lgu |
involves: 129/Sv * BALB/c * C57BL/6 * SLJ | J:91715 | View | ||||
Werner syndrome | Wrntm1Led/Wrntm1Led | B6.129S6(BKSW)-Wrntm1Led | J:106446 | View | ||||
WHIM syndrome 1 | Cxcr4tm1.1Bala/Cxcr4+ | B6.129S2-Cxcr4tm1.1Bala | J:186735 | View | ||||
Williams-Beuren syndrome | Del(5Gtf2i-Fkbp6)1Vcam/+ | B6.129-Del(5Gtf2i-Fkbp6)1Vcam(J:204278) | J:216195 | View | ||||
Williams-Beuren syndrome | Del(5Gtf2i-Limk1)1Uta/Del(5Limk1-Trim50)2Uta | involves: 129S7/SvEvBrd * C57BL/6J | J:182796 | View | ||||
Williams-Beuren syndrome | Eif4hGt(Ex279)Byg/Eif4hGt(Ex279)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:181945 | View | ||||
Wiskott-Aldrich syndrome | Wastm1Sbs/Wastm1Sbs | 129S6/SvEvTac-Wastm1Sbs/J | J:180407 | View | ||||
Wiskott-Aldrich syndrome | Wastm1Sbs/Wastm1Sbs | either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6) | J:48836 | View | ||||
Wolcott-Rallison syndrome | Eif2ak3tm1Drc/Eif2ak3tm1Drc | involves: 129S6/SvEvTac | J:76661 | View | ||||
Wolcott-Rallison syndrome | Eif2ak3tm1Dron/Eif2ak3tm1Dron | involves: 129S6/SvEvTac * Swiss Webster | J:70005 | View | ||||
Wolfram syndrome 1 | Wfs1tm1.1Bedel/Wfs1tm1.1Bedel | involves: C57BL/6N | J:342760 | View | ||||
Wolfram syndrome 1 | Wfs1tm1Koks/Wfs1tm1Koks | 129S6/SvEvTac-Wfs1tm1Koks | J:221943, J:221941 | View | ||||
Wolfram syndrome 1 |
Wfs1tm1Perm/Wfs1tm1Perm Tg(Ins2-cre)23Herr/0 |
involves: 129X1/SvJ * C57BL/6J * CBA/J | J:104712 | View | ||||
Wolfram syndrome 1 | Wfs1tm1Yoka/Wfs1tm1Yoka | B6.Cg-Wfs1tm1Yoka | J:90420 | View | ||||
Wolfram syndrome 1 | Wfs1tm1Yoka/Wfs1tm1Yoka | B6J.129-Wfs1tm1Yoka | J:136108 | View | ||||
Wolfram syndrome 1 | Wfs1tm1Yoka/Wfs1tm1Yoka | involves: 129/Sv * C57BL/6 | J:90420 | View | ||||
Wolman disease | Lipatm1Ggb/Lipatm1Ggb | involves: 129P2/OlaHsd * CF-1 | J:49674 | View | ||||
X-linked adrenal hypoplasia congenita | Nr0b1tm1.1Lja/Y | involves: 129S1/Sv * 129X1/SvJ | J:51292, J:71710 | View | ||||
X-linked agammaglobulinemia |
Blnktm1Pjln/Blnktm1Pjln Btktm1Wk/Btktm1Wk |
involves: 129S4/SvJae * BALB/c * C57BL/6 | J:70406 | View | ||||
X-linked agammaglobulinemia | Btktm1Gsv/Y | involves: 129P2/OlaHsd * C57BL/6 | J:35769 | View | ||||
X-linked agammaglobulinemia | Btktm1Wk/Btktm1Wk | involves: 129S4/SvJae * C57BL/6 | J:28968 | View | ||||
X-linked agammaglobulinemia |
Btktm1Wk/Btktm1Wk Tectm1Welm/Tectm1Welm |
involves: 129P2/OlaHsd * C57BL/6 | J:66080 | View | ||||
X-linked agammaglobulinemia | Btkxid/Btkxid | CBA/HN-Btkxid | J:81429 | View | ||||
X-linked agammaglobulinemia | Btkxid/Btkxid | involves: CBA/HN * DBA/2N | J:81429 | View | ||||
X-linked agammaglobulinemia | Btkxid/Y | CBA/HN-Btkxid | J:81429 | View | ||||
X-linked agammaglobulinemia | Btkxid/Y | involves: CBA/HN * DBA/2N | J:81429 | View | ||||
X-linked Alport syndrome | Col4a5em1Keha/Y | C57BL/6J-Col4a5em1Keha | J:283613 | View | ||||
X-linked Alport syndrome | Col4a5tm1Yseg/Col4a5+ | B6.Cg-Col4a5tm1Yseg | J:102306, J:210414 | View | ||||
X-linked Alport syndrome | Col4a5tm1Yseg/Y | B6.Cg-Col4a5tm1Yseg | J:102306, J:210414 | View | ||||
X-linked cleft palate with or without ankyloglossia | Tbx22tm1.1Sta/Tbx22tm1.1Sta | involves: 129 * CD-1 | J:153100 | View | ||||
X-linked cleft palate with or without ankyloglossia | Tbx22tm1.1Sta/Y | involves: 129/Sv * CD-1 | J:153100 | View | ||||
X-linked cone-rod dystrophy 1 | Rpgrtm1Tili/Rpgrtm1Tili | involves: 129S4/SvJae * C57BL/6 | J:61371 | View | ||||
X-linked cone-rod dystrophy 1 |
Rpgrtm1Tili/Rpgrtm1Tili Tg(CMV-Rpgr)1Tili/0 |
involves: 129S4/SvJae * C57BL/6 | J:87299 | View | ||||
X-linked deafness 4 | Smpxem1Jgao/Smpx+ | CBA/CaJ-Smpxem1Jgao | J:314284 | View | ||||
X-linked deafness 4 | Smpxem1Jgao/Smpxem1Jgao | CBA/CaJ-Smpxem1Jgao | J:314284 | View | ||||
X-linked deafness 4 | Smpxem1Jgao/Y | CBA/CaJ-Smpxem1Jgao | J:314284 | View | ||||
X-linked deafness 4 | Smpxem2Jgao/Smpx+ | CBA/CaJ-Smpxem2Jgao | J:314284 | View | ||||
X-linked deafness 4 | Smpxem2Jgao/Smpxem2Jgao | CBA/CaJ-Smpxem2Jgao | J:314284 | View | ||||
X-linked deafness 4 | Smpxem2Jgao/Y | CBA/CaJ-Smpxem2Jgao | J:314284 | View | ||||
X-linked distal spinal muscular atrophy 3 |
Atp7atm1.1Mjp/Y Mnx1tm4(cre)Tmj/Mnx1+ |
involves: 129S1/Sv * C57BL/6 | J:221066 | View | ||||
X-linked distal spinal muscular atrophy 3 | Atp7atm1.2Mlke/Y | involves: C57BL/6J | J:266704 | View | ||||
X-linked dominant hypophosphatemic rickets |
Fgf23tm1Blan/Fgf23+ PhexHyp/Y |
Not Specified | J:94041 | View | ||||
X-linked dominant hypophosphatemic rickets |
Fgf23tm1Sliu/Fgf23+ PhexHyp/Y |
involves: 129S/SvEv * C57BL/6 | J:110579 | View | ||||
X-linked dominant hypophosphatemic rickets |
Fgf23tm1Sliu/Fgf23tm1Sliu PhexHyp/Y |
involves: 129S/SvEv * C57BL/6 | J:110579 | View | ||||
X-linked dominant hypophosphatemic rickets | Gy/Y | involves: C3H/Sn * C57BL/6Ei | J:38621, J:88352 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexHyp-2J/Phex+ | C57BL/6-PhexHyp-2J/J | J:88352 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexHyp-2J/Y | C57BL/6-PhexHyp-2J/J | J:88352 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexHyp-Duk/Phex+ | involves: BALB/cAnBomUrd | J:88352 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexHyp-Duk/Y | involves: BALB/cAnBomUrd | J:88352 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexHyp/? | involves: C57BL/6J | J:99866 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexHyp/Phex+ | B6.Cg-PhexHyp/J | J:88352 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexHyp/Y | B6.Cg-PhexHyp/J | J:38621, J:67356, J:88352 | View | ||||
X-linked dominant hypophosphatemic rickets | Phexm1Jrt/Phex+ | B6.129S1-PhexM1Jrt | J:196537 | View | ||||
X-linked dominant hypophosphatemic rickets | Phexm1Jrt/Y | B6.129S1-PhexM1Jrt | J:196537 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexMhdabap012/PhexMhdabap012 | C3HeB/FeJ-PhexMhdabap012 | J:183993 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexMhdabap024/Phex+ | C3HeB/FeJ-PhexMhdabap024 | J:264682 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexMhdabap024/PhexMhdabap024 | C3HeB/FeJ-PhexMhdabap024 | J:183993 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexMhdabap024/Y | C3HeB/FeJ-PhexMhdabap024 | J:264682 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexPug/Y | involves: C57BL/6J | J:136463 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexSka1/Phex+ | C57BL/6-PhexSka1 | J:79953 | View | ||||
X-linked dominant hypophosphatemic rickets | PhexSka1/Y | C57BL/6-PhexSka1 | J:79953 | View | ||||
X-linked juvenile retinoschisis 1 | Rs1em1Fegu/Y | involves: C57BL/6J | J:282252 | View | ||||
X-linked juvenile retinoschisis 1 | Rs1tm1.1Rom/Y | involves: 129S6/SvEvTac * C57BL/6NTac | J:285517 | View | ||||
X-linked juvenile retinoschisis 1 | Rs1tm1Sie/Rs1tm1Sie | involves: 129S/SvEv * C57BL/6J | J:93040 | View | ||||
X-linked juvenile retinoschisis 1 | Rs1tm1Sie/Y | involves: 129S/SvEv * C57BL/6J | J:93040 | View | ||||
X-linked juvenile retinoschisis 1 | Rs1tm1Web/Y | involves: 129S1/Sv * C57BL/6 | J:76332 | View | ||||
X-linked juvenile retinoschisis 1 | Rs1tm2.1Rom/Y | involves: 129S6/SvEvTac * C57BL/6NTac | J:285517 | View | ||||
X-linked juvenile retinoschisis 1 | Rs1tm3.1Rom/Y | involves: 129S6/SvEvTac * C57BL/6NTac | J:285517 | View | ||||
X-linked juvenile retinoschisis 1 | Rs1tmgc1/Rs1tmgc1 | involves: C3H/Rl * C57BL/6 | J:99982 | View | ||||
X-linked lymphoproliferative syndrome 1 | Sh2d1atm1Cpt/Sh2d1atm1Cpt | B6.129S4-Sh2d1atm1Cpt | J:97388, J:97690 | View | ||||
X-linked lymphoproliferative syndrome 1 | Sh2d1atm1Cpt/Sh2d1atm1Cpt | C.129S4-Sh2d1atm1Cpt | J:97388 | View | ||||
X-linked lymphoproliferative syndrome 1 | Sh2d1atm1Cpt/Sh2d1atm1Cpt | involves: 129S4/SvJae * BALB/c | J:97756 | View | ||||
X-linked lymphoproliferative syndrome 1 | Sh2d1atm1Cpt/Sh2d1atm1Cpt | involves: 129S4/SvJae * C57BL/6 | J:97756 | View | ||||
X-linked lymphoproliferative syndrome 1 | Sh2d1atm1Lyin/Sh2d1atm1Lyin | involves: 129S2/SvPas * C57BL/6 | J:97346 | View | ||||
X-linked lymphoproliferative syndrome 1 | Sh2d1atm1Lyin/Y | involves: 129S2/SvPas * C57BL/6 | J:97346 | View | ||||
X-linked lymphoproliferative syndrome 1 | Sh2d1atm1Pls/Sh2d1atm1Pls | either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * C57BL/6) | J:70032 | View | ||||
X-linked nephrogenic diabetes insipidus |
Avpr2tm2.1Jwe/Y Tg(CAG-cre/Esr1*)5Amc/0 |
involves: 129 * C57BL/6 | J:324922 | View | ||||
xanthinuria type II | Mocosem2(IMPC)Ics/Mocosem2(IMPC)Ics | involves: C57BL/6N | J:336718 | View | ||||
xeroderma pigmentosum group A |
Ercc2tm2(ERCC2)Jhjh/Ercc2tm2(ERCC2)Jhjh Xpatm1Hvs/Xpatm1Hvs |
involves: 129P2/OlaHsd * C57BL/6 | J:76608 | View | ||||
xeroderma pigmentosum group A | Xpatm1Tnka/Xpatm1Tnka | involves: C57BL/6 * CBA | J:35054 | View | ||||
xeroderma pigmentosum group B | Ercc3tm2Jhjh/Ercc3tm2Jhjh | B6.129P2-Ercc3tm2Jhjh | J:145759 | View | ||||
xeroderma pigmentosum group C | Xpctm1Brd/Xpctm1Brd | involves: 129S7/SvEvBrd * C57BL | J:28708 | View | ||||
xeroderma pigmentosum group D | Ercc2tm3Jhjh/Ercc2tm3Jhjh | involves: 129P2/OlaHsd * C57BL/6 * FVB | J:112689 | View | ||||
xeroderma pigmentosum group E | Ddb2tm1Linn/Ddb2+ | involves: 129S/SvEv * C57BL/6 | J:88125 | View | ||||
xeroderma pigmentosum group E | Ddb2tm1Linn/Ddb2tm1Linn | involves: 129S/SvEv * C57BL/6 | J:88125 | View | ||||
xeroderma pigmentosum group E | Ddb2tm1Pra/Ddb2+ | involves: C57BL/6 | J:95633 | View | ||||
xeroderma pigmentosum group E | Ddb2tm1Pra/Ddb2tm1Pra | involves: C57BL/6 | J:95633 | View | ||||
xeroderma pigmentosum group F | Ercc4tm1Fwa/Ercc4tm1Fwa | involves: 129S6/SvEvTac | J:87684 | View | ||||
xeroderma pigmentosum group G | Ercc5tm1Shm/Ercc5tm1Shm | involves: 129S2/SvPas * C57BL/6J | J:53756 | View | ||||
xeroderma pigmentosum group G | Ercc5tm2Shm/Ercc5tm2Shm | involves: 129S2/SvPas * C57BL/6J | J:89911 | View | ||||
xeroderma pigmentosum group G | Ercc5tm3Shm/Ercc5tm3Shm | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:89911 | View | ||||
xeroderma pigmentosum group G | Ercc5tm4Shm/Ercc5tm4Shm | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:89911 | View | ||||
xeroderma pigmentosum variant type | Polhtm1.1Rak/Polhtm1.1Rak | involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6 | J:105034 | View | ||||
xeroderma pigmentosum variant type | Polhtm1Crey/Polhtm1Crey | involves: 129P2/OlaHsd * C57BL/6 | J:98037 | View | ||||
xeroderma pigmentosum variant type | Polhtm1Fmh/Polhtm1Fmh | involves: C57BL/6 | J:99721 | View | ||||
Xia-Gibbs Syndrome | Ahdc1em#Oro/? | mosaic involves: C57BL/6 * CD-1 | J:326009 | View | ||||
Yunis-Varon syndrome | Fig4plt1/Fig4plt1 | involves: 129P2/OlaHsd * C3H * SJL | J:203638 | View | ||||
Zaki syndrome | Wlsem1Jgg/Wlsem1Jgg | involves: C57BL/6J | J:341542 | View | ||||
Zaki syndrome | Wlsem2Jgg/Wlsem2Jgg | involves: C57BL/6J | J:341542 | View | ||||
![]() | abdominal obesity-metabolic syndrome | Ctf1tm1Msd/Ctf1tm1Msd | B6.Cg-Ctf1tm1Msd | J:176727 | View | |||
abdominal obesity-metabolic syndrome | Gucy2ctm1Gar/Gucy2ctm1Gar | B6.129S6-Gucy2ctm1Gar | J:178241 | View | ||||
abdominal obesity-metabolic syndrome | Lepob/Lepob | involves: STOCK Mlphln a Tgfawa1 Cdh23v Ednrbs | J:219470 | View | ||||
abdominal obesity-metabolic syndrome | Neil1tm1Rsld/Neil1tm1Rsld | involves: 129S1/Sv * C57BL/6 | J:106077 | View | ||||
abdominal obesity-metabolic syndrome | Ppargtm1Lja/Pparg+ | involves: 129S1/Sv * 129X1/SvJ | J:98786 | View | ||||
abdominal obesity-metabolic syndrome |
Prkcitm1Rfar/Prkci+ Tg(Ckmm-cre)5Khn/? |
involves: 129P2/OlaHsd * C57BL/6 * FVB | J:123964 | View | ||||
abdominal obesity-metabolic syndrome | Sirt3tm1.1Fwa/Sirt3tm1.1Fwa | involves: 129S6/SvEvTac | J:178653 | View | ||||
abdominal obesity-metabolic syndrome |
Slc2a9tm1Khm/Slc2a9tm1Khm Tg(Vil1-cre)997Gum/0 |
involves: 129 * C57BL/6 * C57BL/6J | J:221544 | View | ||||
abdominal obesity-metabolic syndrome 1 |
Apobtm2Sgy/Apobtm2Sgy Apoetm1Unc/Apoetm1Unc Lepob/Lepob |
involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6 | J:133453 | View | ||||
abdominal obesity-metabolic syndrome 1 |
Apobtm2Sgy/Apobtm2Sgy Ldlrtm1Her/Ldlrtm1Her Lepob/Lepob |
involves: 129S7/SvEvBrd * C57BL/6 | J:133453 | View | ||||
abdominal obesity-metabolic syndrome 1 | Lepob/Lepob | involves: C57BL/6J | J:219118 | View | ||||
abdominal obesity-metabolic syndrome 1 | Trp53inp1tm1Acar/Trp53inp1tm1Acar | involves: 129/Sv * C57BL/6 | J:233434 | View | ||||
age related macular degeneration | Ccl2tm1Rol/Ccl2tm1Rol | B6.129S4-Ccl2tm1Rol | J:147328 | View | ||||
age related macular degeneration |
Ccl2tm1Rol/Ccl2tm1Rol Cx3cr1tm1Litt/Cx3cr1tm1Litt |
involves: 129P2/OlaHsd * 129S4/SvJae * C57BL/6J | J:200877 | View | ||||
age related macular degeneration |
Ccl2tm1Rol/Ccl2tm1Rol Cx3cr1tm1Zm/Cx3cr1tm1Zm |
involves: 129 * 129S4/SvJae | J:126935 | View | ||||
age related macular degeneration | Ccr2tm1Mae/Ccr2tm1Mae | B6.129P2-Ccr2tm1Mae | J:147328 | View | ||||
age related macular degeneration | Cd46tm1Atk/Cd46tm1Atk | B6.129-Cd46tm1Atk | J:234294 | View | ||||
age related macular degeneration | Ppargc1atm1Brsp/Ppargc1a+ | involves: 129S4/SvJae * C57BL/6 | J:264271 | View | ||||
age related macular degeneration 1 |
Cryba1tm1.1Dbsa/Cryba1tm1.1Dbsa Tg(BEST1-cre)1Jdun/0 |
involves: 129S6/SvEvTac * C57BL/6 | J:215531 | View | ||||
age related macular degeneration 1 | Vldlrtm1Her/Vldlrtm1Her | B6;129S7-Vldlrtm1Her/J | J:132497 | View | ||||
amyotrophic lateral sclerosis type 1 | Sod2tm1Cje/Sod2tm1Cje | involves: C57BL/6J | J:45913 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Thy1-Sncg)HvP36Putt/? | C57BL/6-Tg(Thy1-Sncg)HvP36Putt | J:185793 | View | ||||
amyotrophic lateral sclerosis type 1 | Vegfatm2Pec/Vegfatm2Pec | involves: 129S1/Sv * 129X1/SvJ | J:69797 | View | ||||
amyotrophic lateral sclerosis type 1 | Vps54wr/Vps54wr | involves: C57BL/6J * C57BL/Fa | J:181019, J:196432 | View | ||||
anterior segment dysgenesis |
Tsc1tm1Djk/Tsc1tm1Djk Tg(Lhx2-cre)1Lcar/0 |
involves: 129S4/SvJae * C57BL/6 * CBA | J:239666 | View | ||||
ARC syndrome |
Vipas39tm1c(KOMP)Mbp/Vipas39tm1c(KOMP)Mbp Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+ |
involves: C57BL/6 * C57BL/6J * C57BL/6N | J:236095 | View | ||||
ARC syndrome |
Vps33btm1.1Arte/Vps33btm1.1Arte Gt(ROSA)26Sortm1(cre/ERT2)Tyj/Gt(ROSA)26Sor+ |
involves: C57BL/6 * C57BL/6J | J:222766 | View | ||||
arrhythmogenic right ventricular dysplasia 5 | Rpsatp1/Rpsatp1 | involves: KK | J:87868 | View | ||||
asphyxiating thoracic dystrophy 1 | Ift140cauli/Ift140cauli | involves: C3H/HeH * C57BL/6JAnu | J:220659 | View | ||||
asphyxiating thoracic dystrophy 3 | Ift80Gt(AN0245)Wtsi/Ift80Gt(AN0245)Wtsi | involves: 129P2/OlaHsd | J:169236 | View | ||||
atrichia with papular lesions | Tg(K6ODCtr)55Tgo/0 | C57BL/6-Tg(K6ODCtr)55Tgo/J | J:62356 | View | ||||
autosomal dominant disease | Fgfr3tm1.1Iwa/Fgfr3+ | involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss | J:70061 | View | ||||
autosomal dominant intellectual developmental disorder |
Auts2tm1.1Dare/Auts2tm1.1Dare Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * SJL | J:217675 | View | ||||
autosomal dominant intellectual developmental disorder | Mbd5Gt(Ayu21-B205)Imeg/Mbd5+ | B6.Cg-Mbd5Gt(Ayu21-B205)Imeg | J:212073 | View | ||||
autosomal dominant intellectual developmental disorder |
Zbtb18tm1.1Nda/Zbtb18tm1.1Nda Tg(Nes-cre)1Kln/0 |
involves: C57BL/6 * SJL | J:184434 | View | ||||
autosomal dominant nonsyndromic deafness 4A | Ceacam16tm1Wzm/Ceacam16tm1Wzm | BALB/cJ-Ceacam16tm1Wzm | J:187537 | View | ||||
autosomal dominant nonsyndromic deafness 25 | Trpv4tm1Msz/Trpv4tm1Msz | involves: 129X1/SvJ * C57BL/6 | J:104851 | View | ||||
autosomal dominant polycystic kidney disease | Bicc1jcpk/Bicc1+ | involves: 101 * C3H * T STOCK | J:23047 | View | ||||
autosomal dominant polycystic kidney disease | Nphp3pcy/Nphp3pcy | either: D2.KK-Nphp3pcy or (involves: DBA/2Fg * DBA/2J * KK) | J:11399 | View | ||||
autosomal dominant polycystic kidney disease | Nphp3pcy/Nphp3pcy | involves: KK | J:244067 | View | ||||
autosomal dominant polycystic kidney disease | Nphp3pcy/Nphp3pcy | KK-Nphp3pcy | J:8302 | View | ||||
autosomal dominant polycystic kidney disease | Tg(HBB-Myc)#Cos/0 | involves: C57BL/6J * CBA/J | J:45203 | View | ||||
autosomal recessive Alport syndrome | Mpv17/Mpv17 | CFW-Mpv17/J | J:48653 | View | ||||
autosomal recessive congenital ichthyosis 4B | Cst6ichq/Cst6+ | involves: BALB/cJ | J:41426, J:90417 | View | ||||
autosomal recessive congenital ichthyosis 4B |
Pigatm1Tak/Pigatm1Tak Tg(KRT5-cre)1Tak/0 |
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 | J:91794 | View | ||||
autosomal recessive congenital ichthyosis 4B |
Pigatm1Tak/Y Tg(KRT5-cre)1Tak/0 |
involves: 129S1/Sv * 129X1/SvJ * C3H * C57BL/6 | J:91794 | View | ||||
autosomal recessive congenital ichthyosis 4B |
Prss8tm1.1Hum/Prss8tm1.2Hum Tg(KRT14-cre)1Ipc/0 |
involves: 129/Sv * C57BL/6 * FVB/N * SJL | J:100139 | View | ||||
autosomal recessive disease | Ppp1r13lwa3-J/Ppp1r13lwa3-J | BALB/cJ-Ppp1r13lwa3-J/J | J:264272 | View | ||||
autosomal recessive hypophosphatemic rickets | Dmp1tm1Mis/Dmp1tm1Mis | involves: 129S7/SvEvBrd * CD-1 | J:184352 | 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 nonsyndromic deafness | Atp6v1b1vtx/Atp6v1b1vtx | MRL/MpJ-Atp6v1b1vtx/Kjn | J:243701 | View | ||||
autosomal recessive osteopetrosis 1 | Ccdc154ntl/Ccdc154ntl | involves: 129S7/SvEvBrd * C57BL/6J | J:226596 | View | ||||
autosomal recessive polycystic kidney disease | Arl3Gt(OST263303)Lex/Arl3Gt(OST263303)Lex | involves: 129S5/SvEvBrd | J:107331 | View | ||||
autosomal recessive polycystic kidney disease | Bicc1jcpk-bpk/Bicc1jcpk-bpk | BALB/c-Bicc1jcpk-bpk | J:13276, J:21554, J:36348 | View | ||||
autosomal recessive polycystic kidney disease | Bicc1jcpk-bpk/Bicc1jcpk-bpk | involves: BALB/c * CAST/EiJ | J:36348 | View | ||||
autosomal recessive polycystic kidney disease | Bicc1jcpk/Bicc1jcpk-bpk | involves: 101 * BALB/c * C3H * C57BL/6J * T STOCK | J:36348 | View | ||||
autosomal recessive polycystic kidney disease | Bicc1jcpk/Bicc1jcpk | involves: 101 * C3H * C57BL/6J * T STOCK | J:36348 | View | ||||
autosomal recessive polycystic kidney disease | Bicc1jcpk/Bicc1jcpk | involves: 101 * C3H * T STOCK | J:23047 | View | ||||
autosomal recessive polycystic kidney disease | Bicc1tm1Emdr/Bicc1tm1Emdr | B6SJL-Bicc1tm1Emdr | J:121683 | View | ||||
autosomal recessive polycystic kidney disease | Cys1cpk/Cys1cpk | B6(Cg)-Cys1cpk/J | J:6718, J:9290 | View | ||||
autosomal recessive polycystic kidney disease | Cys1cpk/Cys1cpk | B6(Cg)-Cys1cpk/JUnc | J:7202 | View | ||||
autosomal recessive polycystic kidney disease | Cys1cpk/Cys1cpk | C.B6(Cg)-Cys1cpk | J:99616 | View | ||||
autosomal recessive polycystic kidney disease | Cys1cpk/Cys1cpk | D2J.B6(Cg)-Cys1cpk | J:99620 | View | ||||
autosomal recessive polycystic kidney disease | Cys1cpk/Cys1cpk | involves: C57BL/6J * CD-1 | J:33739 | View | ||||
autosomal recessive polycystic kidney disease | Dzip1lwarpy/Dzip1lwarpy | involves: C3H * C57BL/6 | J:249936 | View | ||||
autosomal recessive polycystic kidney disease | Dzip1lwarpy/Dzip1lwarpy | involves: C57BL/6 * CD-1 | J:249936 | View | ||||
autosomal recessive polycystic kidney disease | Ift88Tg737Rpw/Ift88Tg737Rpw | C3.FVB-Ift88Tg737Rpw | J:18508, J:73583 | View | ||||
autosomal recessive polycystic kidney disease | Ift88Tg737Rpw/Ift88Tg737Rpw | FVB/N-Ift88Tg737Rpw | J:18508, J:37149, J:73583, J:95813 | View | ||||
autosomal recessive polycystic kidney disease | Ift88Tg737Rpw/Ift88Tg737Rpw | involves: C3H * FVB/N | J:73583 | View | ||||
autosomal recessive polycystic kidney disease | Ift88Tg737Rpw/Ift88Tg737Rpw | involves: FVB/N | J:65500, J:90990 | View | ||||
autosomal recessive polycystic kidney disease | Nek1kat-2J/Nek1kat-2J | C57BL/6J-Nek1kat-2J/J | J:37799 | View | ||||
autosomal recessive polycystic kidney disease | Nek1kat/Nek1kat | involves: C3HeB/FeJLe * C57BL/6J * RBF/Dn | J:37799 | View | ||||
autosomal recessive polycystic kidney disease | Nek8jck/Nek8jck | involves: C57BL/6J | J:11885 | View | ||||
autosomal recessive polycystic kidney disease | Pkd1m1Bei/Pkd1m1Bei | involves: A/J * FVB/N | J:75360 | View | ||||
autosomal recessive polycystic kidney disease | Sclt1Tg(CAG-sb10)1Dla/Sclt1Tg(CAG-sb10)1Dla | FVB/N-Sclt1Tg(CAG-sb10)1Dla | J:243427 | View | ||||
autosomal recessive polycystic kidney disease | Tg(Pkd1)26Mtru/0 | involves: C57BL/6J * CBA/J | J:157952 | View | ||||
autosomal recessive polycystic kidney disease |
Tsc1tm1Djk/Tsc1tm1Djk Tg(Pax8-rtTA2S*M2)1Koes/0 Tg(tetO-cre)LC1Bjd/0 |
involves: 129S4/SvJae * BALB/c * C57BL/6 * DBA | J:140925 | View | ||||
autosomal recessive pseudohypoaldosteronism type 1 | Scnn1btm1Wsh/Scnn1btm1Wsh | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:53058 | View | ||||
autosomal recessive pseudohypoaldosteronism type 1 | Scnn1gtm1Bhk/Scnn1gtm1Bhk | involves: 129P2/OlaHsd * C57BL/6 * DBA/2 | J:50528 | View | ||||
autosomal recessive Robinow syndrome | Prickle1tm1Asw/Prickle1tm1.2Asw | Not Specified | J:213772 | View | ||||
autosomal recessive Robinow syndrome | Prickle1tm1Asw/Prickle1tm1Asw | Not Specified | J:213772 | View | ||||
Axenfeld-Rieger syndrome type 1 | Tg(KRT14-Hmgn2)#Baam/0 | Not Specified | J:203117 | View | ||||
Axenfeld-Rieger syndrome type 3 | Bmp4tm1Blh/Bmp4+ | B6.129S2-Bmp4tm1Blh | J:82877 | View | ||||
Bardet-Biedl syndrome | Tbc1d32b2b2284Clo/Tbc1d32b2b2284Clo | C57BL/6J-Tbc1d32b2b2284Clo | J:175213 | View | ||||
Barth syndrome | Fkbp1atm1Zuk/Fkbp1atm1Zuk | either: (involves: 129S7/SvEvBrd) or (involves: 129S7/SvEvBrd * C57BL/6J) | J:45536 | View | ||||
Barth syndrome | Mesttm1Masu/Mest+ | involves: 129S1/Sv * 129X1/SvJ | J:79223 | View | ||||
Bartter disease | Clcnkbtm1.1Doel/Clcnkbtm1.1Doel | involves: 129S1/Sv * 129X1/SvJ | J:259639 | View | ||||
beta thalassemia | Klf1tm1Sho/Klf1tm1Sho | involves: 129S4/SvJae * C57BL/6 | J:25651 | View | ||||
blepharophimosis, ptosis, and epicanthus inversus syndrome | E330023G01RikTn(pb-Act-RFP)1.1Zhu/E330023G01RikTn(pb-Act-RFP)1.1Zhu | involves: FVB/N | J:210665 | View | ||||
Bloom syndrome |
Nsmce2tm2.1Ofc/Nsmce2tm2.1Ofc Ndor1Tg(UBC-cre/ERT2)1Ejb/0 |
involves: 129S/SvEv * C57BL/6 * SJL | J:227197 | View | ||||
buphthalmos | Foxc1tm1Blh/Foxc1+ | B6.Cg-Foxc1tm1Blh | J:82280 | View | ||||
buphthalmos |
Foxc1tm1Blh/Foxc1+ Tyrc-2J/Tyrc-2J |
B6.Cg-Tyrc-2J Foxc1tm1Blh | J:82280 | View | ||||
buphthalmos | Tyrc-2J/Tyrc-2J | B6(Cg)-Tyrc-2J/J | J:82280 | View | ||||
Camurati-Engelmann disease | Mitfmi-ew/Mitfmi-ew | involves: C57BL/6Bn * NAW | J:89821 | View | ||||
Canavan disease | Sod2tm1Cje/Sod2tm1Cje | involves: C57BL/6J | J:45913 | View | ||||
cardiofaciocutaneous syndrome | Map2k1tm2.1Chrn/Map2k1tm2.1Chrn | involves: 129S6/SvEvTac * C57BL/6 * CBA * SJL/J | J:261678 | View | ||||
Caroli syndrome | Pkhd1cyli/Pkhd1cyli | D2.Cg-(D4Mit42-D4Smh6b) Pkhd1cyli/EiJ | J:343537 | View | ||||
cataract | Acc/Acc+ | involves: 101 * C3H | J:9528 | View | ||||
cataract | Alm/Alm+ | involves: 101 * C3H | J:6686 | View | ||||
cataract | Apo/Apo+ | involves: 101 * C3H | J:9528 | View | ||||
cataract | Apoca/Apoca+ | involves: 101 * C3H | J:9528 | View | ||||
cataract | Cat2no2/Cat2+ | DBA/2-Cat2no2 | J:16569 | View | ||||
cataract | Cat4Apcat1-2/Cat4+ | involves: 101 * C3H | J:6686, J:9528 | View | ||||
cataract | Cat4Apcat1-3/Cat4+ | involves: 101 * C3H | J:9528 | View | ||||
cataract | Cat4Apcat1-4/Cat4+ | involves: 101 * C3H | J:1598 | View | ||||
cataract | Ccw/Ccw+ | involves: unpedigreed stock | J:34877, J:66649 | View | ||||
cataract | Coc/Coc | involves: 101 * C3H * C57BL/6 | J:9528 | View | ||||
cataract | Coc/Coc+ | involves: 101 * C3H * C57BL/6 | J:9528 | View | ||||
cataract | Cryga1Neu/Cryga+ | involves: 101 * C3H | J:21950 | View | ||||
cataract | CrygeAey1/Cryge+ | C3HeB/FeJ-CrygeAey1 | J:68708 | View | ||||
cataract | CrygeAey1/CrygeAey1 | C3HeB/FeJ-CrygeAey1 | J:68708 | View | ||||
cataract | Dnase2btm1Osa/Dnase2btm1Osa | Not Specified | J:85215 | View | ||||
cataract | Enc/Enc+ | involves: 101 * C3H | J:9528 | View | ||||
cataract |
Gclctm1c(EUCOMM)Wtsi/Gclctm1c(EUCOMM)Wtsi Tg(Cryaa-cre)10Mlr/0 |
involves: 129S4/SvJaeSor * C57BL/6N * FVB/N | J:194778 | View | ||||
cataract | Iac/Iac+ | involves: 101 * C3H | J:9528 | View | ||||
cataract | Idc/Idc+ | involves: 101 * C3H | J:9528 | View | ||||
cataract | Nuca/Nuca+ | involves: 101 * C3H | J:6686 | View | ||||
cataract | SordC57BL/Lia/SordC57BL/Lia | involves: C57BL/LiA | J:142446 | View | ||||
cataract | Tcm/Tcm+ | involves: 101 * C3H | J:9528 | View | ||||
cataract | Vps13btm1.2Ics/Vps13btm1.2Ics | involves: C57BL/6N | J:296007 | View | ||||
cataract 2 multiple types | CrygdLop12/Crygd+ | involves: BALB/cJ * SJL/J | J:60856 | View | ||||
catecholaminergic polymorphic ventricular tachycardia | Fkbp1btm1Amks/Fkbp1btm1Amks | DBA/1LacJ-Fkbp1btm1Amks | J:107733 | View | ||||
central conducting lymphatic anomaly | Mdficem1Nlh/Mdficem2Nlh | C57BL/6J-Mdficem1Nlh/Mdficem2Nlh | J:326462 | View | ||||
Charlevoix-Saguenay spastic ataxia | Ankfy1Gt(RRE069)Byg/Ankfy1+ | B6.129P2-Ankfy1Gt(RRE069)Byg | J:250135 | View | ||||
chromosome 1q41-q42 deletion syndrome | Trp53bp2tm1Xlu/Trp53bp2tm1Xlu | B6.129S6-Trp53bp2tm1Xlu | J:240594 | View | ||||
chromosome 1q41-q42 deletion syndrome | Trp53bp2tm1Xlu/Trp53bp2tm1Xlu | C.129S6-Trp53bp2tm1Xlu | J:240594 | View | ||||
chromosome 1q41-q42 deletion syndrome | Trp53bp2tm1Xlu/Trp53bp2tm1Xlu | involves: 129S6/SvEvTac * C57BL/6J | J:240594 | View | ||||
ciliopathy | Kif7b2b2254Clo/Kif7b2b2254Clo | C57BL/6J-Kif7b2b2254Clo | J:175213 | View | ||||
ciliopathy | Sclt1Tg(CAG-sb10)1Dla/Sclt1Tg(CAG-sb10)1Dla | FVB/N-Sclt1Tg(CAG-sb10)1Dla | J:243427 | View | ||||
ciliopathy |
Spry2tm1.1Mrt/Spry2+ Spry4tm1.2Mrt/Spry4tm1.2Mrt |
involves: 129P2/OlaHsd | J:315670 | View | ||||
ciliopathy | Spry2tm1.1Mrt/Spry2tm1.1Mrt | involves: 129P2/OlaHsd | J:315670 | View | ||||
ciliopathy |
Spry2tm1.1Mrt/Spry2tm1.1Mrt Spry4tm1.2Mrt/Spry4+ |
involves: 129P2/OlaHsd | J:315670 | View | ||||
ciliopathy | Wdr11Gt(Ayu21-KBW205)Imeg/Wdr11Gt(Ayu21-KBW205)Imeg | B6.Cg-Wdr11Gt(Ayu21-KBW205)Imeg | J:257035 | View | ||||
ciliopathy | Wdr19twto/Wdr19twto | involves: FVB/NJ | J:181888 | View | ||||
cleidocranial dysplasia | Ccd/Ccd+ | B10Rl.101-Ccd | J:16170 | View | ||||
cleidocranial dysplasia | Ccd/Ccd+ | involves: 101 * C3H | J:14006 | View | ||||
Coffin-Siris syndrome |
Arid1atm1.1Mag/Arid1a+ H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: C57BL/6J * CBA/J | J:231470 | View | ||||
Coffin-Siris syndrome |
Arid1atm1.1Mag/Arid1atm1.1Mag H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: C57BL/6J * CBA/J | J:231470 | View | ||||
common variable immunodeficiency | Icostm1Flv/Icostm1Flv | involves: 129/Sv * C57BL/6 | J:87123 | View | ||||
common variable immunodeficiency | Icostm1Shr/Icostm1Shr | Not Specified | J:87124 | View | ||||
common variable immunodeficiency | Nfkb2Lym1/Nfkb2+ | BALB/c-Nfkb2Lym1 | J:206674 | View | ||||
common variable immunodeficiency | Nfkb2Lym1/Nfkb2Lym1 | involves: BALB/c | J:206674 | View | ||||
common variable immunodeficiency | Nfkb2tm2Brv/Nfkb2tm2Brv | involves: 129S1/Sv * C57BL/6 | J:206674 | View | ||||
cone-rod dystrophy 19 | rd22/rd22 | B6.Cg-rd22/BocJ | J:347903 | View | ||||
congenital amegakaryocytic thrombocytopenia | Mpltm1Fjs/Mpltm1Fjs | involves: 129 * C57BL/6J | J:87416 | View | ||||
congenital central hypoventilation syndrome | Tlx3tm1Sjk/Tlx3tm1Sjk | involves: 129X1/SvJ | J:60751 | View | ||||
congenital generalized lipodystrophy type 2 | Ppargtm2(tTA)Yba/Pparg+ | involves: 129S1/SvImJ * C57BL/6 | J:125992 | View | ||||
congenital generalized lipodystrophy type 2 | Ppargtm3(tTA)Yba/Pparg+ | involves: 129S1/SvImJ * C57BL/6 | J:125992 | View | ||||
Cornelia de Lange syndrome | Pds5aGt(RRM243)Byg/Pds5aGt(RRM243)Byg | involves: 129/Sv * 129P2/OlaHsd * C57BL/6 | J:148890 | View | ||||
cystic fibrosis | Tg(Scgb1a1-Scnn1b)6608Bouc/0 | involves: C3H * C57BL/6 | J:91139 | View | ||||
DiGeorge syndrome | Aldh1a2tm1Dll/Aldh1a2tm1Ipc | involves: CD-1 | J:81969 | View | ||||
DiGeorge syndrome | b2b954Clo/b2b954Clo | C57BL/6J-b2b954Clo | J:175213 | View | ||||
DiGeorge syndrome | b2b1941Clo/b2b1941Clo | C57BL/6J-b2b1941Clo | J:175213 | View | ||||
DiGeorge syndrome | b2b2696Clo/b2b2696Clo | C57BL/6J-b2b2696Clo | J:175213 | View | ||||
DiGeorge syndrome | Chrdtm1Emdr/Chrdtm1Emdr | either: B6SJL.129-Chrdtm1Emdr or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * SJL/J) | J:83662 | View | ||||
DiGeorge syndrome | Crkltm1Imo/Crkltm1Imo | involves: 129S4/SvJaeSor * C57BL/6J | J:67826 | View | ||||
DiGeorge syndrome |
Dicer1tm1Bdh/Dicer1tm1Bdh H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129 * C57BL/6 * CBA/J | J:166758 | View | ||||
DiGeorge syndrome | Dock1b2b3190Clo/Dock1b2b3190Clo | C57BL/6J-Dock1b2b3190Clo | J:175213 | View | ||||
DiGeorge syndrome |
Fgf8tm1.3Mrt/Fgf8tm1.4Mrt Tg(Tbx1-cre)1Joe/0 |
involves: 129P2/OlaHsd | J:88814 | View | ||||
DiGeorge syndrome | Foxn1nu/Foxn1nu | Not Specified | J:202300 | View | ||||
DiGeorge syndrome | Hoxa3tm1Mrc/Hoxa3tm1Mrc | involves: 129S7/SvEvBrd | J:17753 | View | ||||
DiGeorge syndrome | Kat6atm1Avo/Kat6atm1Avo | involves: 129/Sv * BALB/c * FVB/N | J:188772 | View | ||||
DiGeorge syndrome | Ndst1b2b2230Clo/Ndst1b2b2230Clo | C57BL/6J-Ndst1b2b2230Clo | J:175213 | View | ||||
DiGeorge syndrome | Plxnd1b2b1863Clo/Plxnd1b2b1863Clo | C57BL/6J-Plxnd1b2b1863Clo | J:175213 | View | ||||
DiGeorge syndrome | Plxnd1b2b3150Clo/Plxnd1b2b3150Clo | C57BL/6J-Plxnd1b2b3150Clo | J:175213 | View | ||||
DiGeorge syndrome | pta/pta | C57BL/6J-pta | J:94456 | View | ||||
DiGeorge syndrome |
Tgfbr2tm1Karl/Tgfbr2tm1Karl H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:96359 | View | ||||
DiGeorge syndrome | Vegfatm1Pec/Vegfatm1Pec | involves: 129S1/Sv * 129X1/SvJ | J:81698 | View | ||||
DiGeorge syndrome | Vegfatm4Pec/Vegfatm4Pec | involves: 129S1/Sv * 129X1/SvJ | J:81698 | View | ||||
DiGeorge syndrome | Zfp366b2b2834Clo/Zfp366b2b2834Clo | C57BL/6J-Zfp366b2b2834Clo | J:175213 | View | ||||
dilated cardiomyopathy 1A |
Dot1ltm1Tche/Dot1ltm1.1Tche Tg(Myhca-cre)1Abel/0 |
Not Specified | J:168140 | View | ||||
Duchenne muscular dystrophy | Tg(ACTA1-Ctss)1Jmol/? | FVB/N-Tg(ACTA1-Ctss)1Jmol | J:230788 | View | ||||
Ehlers-Danlos syndrome classic type 1 | Col5a2tm1.2Dgr/Col5a2+ | involves: 129S7/SvEvBrd * C57BL/6 * DBA/2 | J:223298 | View | ||||
Ehlers-Danlos syndrome classic type 1 |
Fmodtm1Aol/Fmodtm1Aol Lumtm1Chak/Lumtm1Chak |
involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:79115 | View | ||||
Ehlers-Danlos syndrome classic type 1 | Lumtm1Chak/Lumtm1Chak | involves: 129S/Sv * CD-1 | J:48068 | View | ||||
enhanced S-cone syndrome | Nrltm1Asw/Nrltm1Asw | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:175566 | View | ||||
epidermolysis bullosa simplex Dowling-Meara type | Krt5tm1Tmm/Krt5tm1Tmm | involves: 129P2/OlaHsd * BALB/c | J:76311 | View | ||||
epidermolysis bullosa simplex Dowling-Meara type |
Krt14tm1Der/Krt14+ Tg(KRT5-cre/PGR)1Der/? |
involves: 129X1/SvJ * FVB * ICR | J:67320 | View | ||||
epidermolysis bullosa simplex Dowling-Meara type |
Krt14tm1Der/Krt14+ Tg(KRT14-cre/PGR)1Der/? |
involves: 129X1/SvJ * FVB * ICR | J:67320 | View | ||||
epidermolysis bullosa simplex Dowling-Meara type | Krt14tm2Der/Krt14+ | involves: 129X1/SvJ | J:67320 | View | ||||
familial adenomatous polyposis | ApcM1Tno/Apc+ | either: B6JJcl.B6(D2JJcl)-ApcM1Tno or (involves: C57BL/6 * C57BL/6JJcl * DBA/2JJcl) | J:218227 | View | ||||
familial adenomatous polyposis | ApcMin/Apc+ | C57BL/6J-ApcMin | J:86036 | View | ||||
familial adenomatous polyposis | ApcMin/Apc+ | involves: AKR/J * C57BL/6J | J:830 | View | ||||
familial adenomatous polyposis |
ApcMin/Apc+ Rab25tm1Jrgo/Rab25tm1Jrgo |
B6.Cg-Rab25tm1Jrgo ApcMin | J:158733 | View | ||||
familial adenomatous polyposis | Apctm1Cip/Apc+ | involves: 129P2/OlaHsd * C57BL/6 | J:94108 | View | ||||
familial adenomatous polyposis |
Apctm1Kk/Apctm1Kk Tg(Lck-cre)1Cwi/? |
involves: 129S6/SvEvTac * C57BL/6 * DBA/2 | J:128606 | View | ||||
familial adenomatous polyposis | Apctm1Mmt/Apc+ | involves: 129S2/SvPas * C57BL/6J | J:25200 | View | ||||
familial adenomatous polyposis | Apctm1Rak/Apc+ | involves: 129P2/OlaHsd * C57BL/6 | J:20443 | View | ||||
familial adenomatous polyposis | Apctm1Tno/Apctm1Tno | involves: 129S4/SvJae * C57BL/6 | J:43301 | View | ||||
familial adenomatous polyposis | Apctm2Tno/Apc+ | involves: C57BL/6J | J:86036 | View | ||||
familial medullary thyroid carcinoma | Prlrtm1Cnp/Prlrtm1Cnp | involves: 129/Sv * 129P2/OlaHsd | J:101609 | View | ||||
fibrodysplasia ossificans progressiva | Tg(Eno2-Bmp4)3Jake/0 | involves: BALB/c * C57BL/6 | J:93682 | View | ||||
Fraser syndrome | Fras1bfb/Fras1bfb | involves: C57BL/6JAnu | J:208682 | View | ||||
Fraser syndrome | Fras1bl/Fras1bl | involves: 101/H * C3H/HeH | J:83745 | View | ||||
Fraser syndrome |
Fras1bl/Fras1bl Frem2my-Ucl/Frem2my-Ucl |
involves: 101/H * C3H/HeH * NMRI | J:98344 | View | ||||
Fraser syndrome | Fras1rdf/Fras1rdf | involves: C57BL/6J * FVB/NJ | J:231083 | View | ||||
Fraser syndrome | Fras1tm1Chpk/Fras1tm1Chpk | involves: 129S1/Sv * 129X1/SvJ * C57BL/10 | J:83746 | View | ||||
Fraser syndrome | Fras1tm1Chpk/Fras1tm1Chpk | involves: 129S1/Sv * 129X1/SvJ * NMRI | J:137010 | View | ||||
Fraser syndrome | Frem1bat/Frem1bat | C57BL/6J-Frem1bat | J:92613 | View | ||||
Fraser syndrome | Frem1bfd/Frem1bfd | involves: C57BL/6J | J:92613 | View | ||||
Fraser syndrome | Frem1heb/Frem1heb | involves: AKR/J | J:92613 | View | ||||
Fraser syndrome | Frem1tm1Ksek/Frem1tm1Ksek | involves: 129 * C57BL/6 | J:111788 | View | ||||
Fraser syndrome | Frem2b2b1562Clo/Frem2b2b1562Clo | C57BL/6J-Frem2b2b1562Clo | J:175213 | View | ||||
Fraser syndrome | Frem2Gt(KST252)Byg/Frem2my-Ucl | involves: 129P2/OlaHsd * CD-1 * NMRI | J:98344 | View | ||||
Fraser syndrome | Frem2my-Ucl/Frem2my-Ucl | involves: NMRI | J:98344 | View | ||||
Fraser syndrome | Frem2my/Frem2my | MY/HuLeJ | J:111788 | View | ||||
Fraser syndrome | Frem2ne/Frem2ne | STOCK Frem2ne/GrsrJ | J:185265, J:222308 | View | ||||
Fraser syndrome | Grip1eb/Grip1eb | involves: ATEB/Le * C57BL/6J | J:111788 | View | ||||
Fraser syndrome | Grip1tm1Rha/Grip1tm1Rha | B6.129-Grip1tm1Rha | J:88266 | View | ||||
Gitelman syndrome | Stk39tm1.2Slin/Stk39tm1.2Slin | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:165706 | View | ||||
Gitelman syndrome | Stk39tm1Pawe/Stk39tm1Pawe | involves: 129S6/SvEvTac * C57BL/6J | J:287773 | View | ||||
Gitelman syndrome | Stk39tm2.1Arte/Stk39tm2.1Arte | involves: C57BL/6J | J:224087 | View | ||||
Gitelman syndrome | Wnk4tm1Pfi/Wnk4tm1Pfi | involves: 129S6/SvEvTac * C57BL/6J | J:184790 | View | ||||
glycogen storage disease Ia | Slc37a4tm1Jyc/Slc37a4tm1Jyc | involves: 129S4/SvJae * C57BL/6 | J:86005 | View | ||||
glycogen storage disease V |
Hif1atm3Rsjo/Hif1atm3Rsjo Tg(Ckmm-cre)5Khn/? |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N | J:97761 | View | ||||
glycogen storage disease VII |
Hif1atm3Rsjo/Hif1atm3Rsjo Tg(Ckmm-cre)5Khn/? |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N | J:97761 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Camk2a-Tardbp)#Ckjs/Tg(Camk2a-Tardbp)#Ckjs | FVB/N-Tg(Camk2a-Tardbp)#Ckjs | J:163612 | View | ||||
hereditary multiple exostoses | Ext2tm1Werb/Ext2+ | involves: C57BL/6 | J:103125 | View | ||||
hereditary spherocytosis type 1 | Add2tm1Llp/Add2tm1Llp | involves: 129S4/SvJae * C57BL/6J | J:71029 | View | ||||
hereditary spherocytosis type 1 | Epb42tm1Llp/Epb42tm1Llp | involves: 129P2/OlaHsd * C57BL/6J | J:67412 | View | ||||
hereditary spherocytosis type 1 | Spta1sph-2Bc/Spta1sph-2Bc | involves: SELH | J:7048, J:7501 | View | ||||
hereditary spherocytosis type 1 | Spta1sph-ha/Spta1sph-ha | involves: DBA/1J | J:14946, J:30699 | View | ||||
hereditary spherocytosis type 1 | Spta1sph/Spta1sph | involves: C3H | J:12276 | View | ||||
hereditary spherocytosis type 4 | Slc4a1wan/Slc4a1wan | C3H/HeJ-Slc4a1wan/J | J:89043 | View | ||||
Hermansky-Pudlak syndrome | Bloc1s4cno/Bloc1s4cno | C3H/HeJ-Bloc1s4cno | J:61187 | View | ||||
Hermansky-Pudlak syndrome | Bloc1s4cno/Bloc1s4cno | involves: C3H/HeJ | J:80751 | View | ||||
Hermansky-Pudlak syndrome | Kxd1tm1Wli/Kxd1tm1Wli | involves: 129 * C57BL/6J | J:192646 | View | ||||
Hermansky-Pudlak syndrome | Rabggtagm/Rabggtagm | C57BL/6J-Rabggtagm | J:13419, J:12434 | View | ||||
Hermansky-Pudlak syndrome | Slc7a11sut/Slc7a11sut | C3H/HeSnJ-Slc7a11sut/J | J:31616 | View | ||||
Hermansky-Pudlak syndrome | Vps33abf/Vps33abf | C57BL/6J-Vps33abf | J:88018 | View | ||||
Hermansky-Pudlak syndrome 1 | Ap3d1mh-4J/Ap3d1mh-4J | involves: 129P2/OlaHsd * BALB/cByJ * C57BL/6J | J:207448 | View | ||||
Hermansky-Pudlak syndrome 1 | Rab27aash/Rab27aash | C3H/HeSn-Rab27aash/J | J:77395 | View | ||||
Hermansky-Pudlak syndrome 2 | Ap3d1mh/Ap3d1mh | B6.C3-Grxcr1pi | J:29151 | View | ||||
Holt-Oram syndrome | vsd/vsd | C57BL/6J-vsd | J:94456 | View | ||||
Holt-Oram syndrome | vsd/vsd+ | C57BL/6J-vsd | J:94456 | View | ||||
hydrolethalus syndrome | Kif7b2b2254Clo/Kif7b2b2254Clo | C57BL/6J-Kif7b2b2254Clo | J:175213 | View | ||||
hyperphosphatemic familial tumoral calcinosis | Galnt3tcal/Galnt3tcal | involves: C3H * C57BL/6J | J:187064 | View | ||||
hyperphosphatemic familial tumoral calcinosis | Galnt3tm1Mjec/Galnt3tm1Mjec | involves: 129S/SvEv * C57BL/6J | J:151805 | View | ||||
hyperphosphatemic familial tumoral calcinosis | Klecalc1/Klecalc1 | involves: C3H/HeH * C57BL/6J | J:229255 | View | ||||
hyperphosphatemic familial tumoral calcinosis | Klecalc2/Klecalc2 | involves: C3H/HeH * C57BL/6J | J:229255 | View | ||||
hypochondrogenesis | Tg(Col2a1*G574S)1Waho/0 | involves: C57BL/6 * DBA/2 | J:38204 | View | ||||
hypotrichosis 4 | HrHp/HrHp | BALB/cJ-HrHp | J:150720 | View | ||||
ichthyosis vulgaris | Lbric-J/Lbric-J | involves: 129S4/SvJae * C57BL/6 | J:143838 | View | ||||
idiopathic pulmonary fibrosis | Tg(H2-K-Fosl2,-EGFP)13Wag/0 | either: 129.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag or B6.Cg-Tg(H2-K-Fosl2,-EGFP)13Wag | J:139032 | View | ||||
idiopathic pulmonary fibrosis | Tg(SFTPC-Tnf)2Pva/0 | involves: C57BL/6 * DBA/2 | J:28120 | View | ||||
inflammatory bowel disease 1 | Nod2tm1Mka/Nod2tm1Mka | involves: C57BL/6 | J:96128 | View | ||||
inflammatory bowel disease 12 | Gnai2tm1Lbi/Gnai2tm1Lbi | involves: 129S7/SvEvBrd | J:24434, J:30507 | View | ||||
inflammatory bowel disease 12 | Gnai2tm1Lbi/Gnai2tm1Lbi | involves: 129S7/SvEvBrd * C57BL/6 | J:91100 | View | ||||
inflammatory bowel disease 12 | Gnai2tm1Lbi/Gnai2tm1Lbi | involves: 129S7/SvEvBrd * C57BL/6J | J:24434 | View | ||||
inflammatory bowel disease 16 | Tg(Csf1r-Tnfsf15,-EGFP)#Targ/0 | involves: C57BL/6 | J:169462 | View | ||||
inflammatory bowel disease 16 | Tg(Lck-Tnfsf15,-EGFP)#Targ/0 | involves: C57BL/6 | J:169462 | View | ||||
Joubert syndrome | Zic1tm1Jaru/Zic1+ | B6.129S4-Zic1tm1Jaru | J:72342 | View | ||||
junctional epidermolysis bullosa Herlitz type | Itga6tm1Egl/Itga6tm1Egl | either: (involves: 129S2/SvPas * C57BL/6) or (involves: 129S2/SvPas * C57BL/6 * CD-1) | J:33712 | View | ||||
junctional epidermolysis bullosa Herlitz type | Lamb3IAP/Lamb3IAP | involves: C3H * C57BL/6 | J:42382 | View | ||||
junctional epidermolysis bullosa Herlitz type | Lamb3tm1.1Hosc/Lamb3tm1.1Hosc | involves: 129S4/SvJae * C57BL/6 | J:218616 | View | ||||
junctional epidermolysis bullosa Herlitz type | Lamc2tm1Uit/Lamc2tm1Uit | involves: C57BL/6 | J:85981 | View | ||||
junctional epidermolysis bullosa non-Herlitz type | Col17a1tm1Shzu/Col17a1tm1Shzu | B6.129S-Col17a1tm1Shzu | J:121695 | View | ||||
junctional epidermolysis bullosa non-Herlitz type | Itgb4tm1Efu/Itgb4tm1Efu | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:77644 | View | ||||
junctional epidermolysis bullosa non-Herlitz type | Lama3tm1Crt/Lama3tm1Crt | involves: 129 * C57BL/6J | J:55865 | View | ||||
junctional epidermolysis bullosa non-Herlitz type | Lamb3IAP/Lamb3IAP | involves: C3H * C57BL/6 | J:42382 | View | ||||
junctional epidermolysis bullosa non-Herlitz type | Lamc2jeb/Lamc2jeb | 129X1/SvJ-Lamc2jeb | J:158873 | View | ||||
juvenile glaucoma |
Pax6tm2Pgr/Pax6+ Tg(Pax6-cre,GFP)1Pgr/0 |
involves: 129S1/Sv * 129X1/SvJ * FVB | J:163191 | View | ||||
Kartagener syndrome | Ap1b1b2b1660Clo/Ap1b1b2b1660Clo | C57BL/6J-Ap1b1b2b1660Clo | J:175213 | View | ||||
Kartagener syndrome | b2b1200Clo/b2b1200Clo | C57BL/6J-b2b1200Clo | J:175213 | View | ||||
Kartagener syndrome | b2b1519Clo/b2b1519Clo | C57BL/6J-b2b1519Clo | J:175213 | View | ||||
Kartagener syndrome | b2b1700Clo/b2b1700Clo | C57BL/6J-b2b1700Clo | J:175213 | View | ||||
Kartagener syndrome | b2b2350Clo/b2b2350Clo | C57BL/6J-b2b2350Clo | J:175213 | View | ||||
Kartagener syndrome | Ccdc39b2b1304Clo/Ccdc39b2b1304Clo | C57BL/6J-Ccdc39b2b1304Clo | J:175213 | View | ||||
Kartagener syndrome | Ccdc39b2b1735Clo/Ccdc39b2b1735Clo | C57BL/6J-Ccdc39b2b1735Clo | J:175213 | View | ||||
Kartagener syndrome | Daw1b2b1116Clo/Daw1b2b1116Clo | C57BL/6J-Daw1b2b1116Clo | J:175213 | View | ||||
Kartagener syndrome | Daw1b2b1584Clo/Daw1b2b1584Clo | C57BL/6J-Daw1b2b1584Clo | J:175213 | View | ||||
Kartagener syndrome | Dnaaf3b2b1739Clo/Dnaaf3b2b1739Clo | C57BL/6J-Dnaaf3b2b1739Clo | J:175213 | View | ||||
Kartagener syndrome | Dnai2b2b3405Clo/Dnai2b2b3405Clo | C57BL/6J-Dnai2b2b3405Clo | J:175213 | View | ||||
Kartagener syndrome | Drc1b2b1654Clo/Drc1b2b1654Clo | C57BL/6J-Drc1b2b1654Clo | J:175213 | View | ||||
Kartagener syndrome | Drc1b2b2237Clo/Drc1b2b2237Clo | C57BL/6J-Drc1b2b2237Clo | J:175213 | View | ||||
Kartagener syndrome | Foxj1tm1Bph/Foxj1tm1Bph | involves: 129S1/Sv * 129X1/SvJ * Black Swiss | J:50025 | View | ||||
Kartagener syndrome | Foxj1tm1Slb/Foxj1tm1Slb | involves: 129X1/SvJ | J:73616 | View | ||||
Kartagener syndrome | Gm572b2b1167Clo/Gm572b2b1167Clo | C57BL/6J-Gm572b2b1167Clo | J:175213 | View | ||||
Kartagener syndrome | Odad2b2b643Clo/Odad2b2b643Clo | C57BL/6J-Odad2b2b643Clo | J:175213 | View | ||||
Kartagener syndrome | Odad3b2b1885Clo/Odad3b2b1885Clo | C57BL/6J-Odad3b2b1885Clo | J:175213 | View | ||||
Kartagener syndrome | Slit2b2b1200.1Clo/Slit2b2b1200.1Clo | C57BL/6J-Slit2b2b1200.1Clo | J:175213 | View | ||||
lacrimoauriculodentodigital syndrome 1 | Fgf10tm1Wss/Fgf10+ | involves: 129X1/SvJ | J:237227 | View | ||||
Lafora disease | Epm2atm1Kzy/Epm2atm1Kzy | involves: 129P2/OlaHsd * C57BL/6J | J:76688, J:173769 | View | ||||
Lafora disease | Nhlrc1tm1(KOMP)Vlcg/Nhlrc1tm1(KOMP)Vlcg | involves: C57BL/6J * C57BL/6NTac | J:165994, J:218959 | 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 | ||||
leukocyte adhesion deficiency 3 | Rasgrp2tm1Amg/Rasgrp2tm1Amg | Not Specified | J:122618 | View | ||||
leukoencephalopathy with vanishing white matter | Eif2b4tm1.1Vdk/Eif2b4tm1.1Vdk | involves: C57BL/6 * C57BL/6J | J:234659 | View | ||||
Loeys-Dietz syndrome |
Fbn1tm1Hcd/Fbn1+ Tgfb2tm1Doe/Tgfb2+ |
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6J | J:188799 | View | ||||
Loeys-Dietz syndrome | Tgfb2tm1Doe/Tgfb2+ | STOCK Tgfb2tm1Doe/J | J:188799 | View | ||||
Loeys-Dietz syndrome | Tgfbr1tm1.1Hcd/Tgfbr1+ | 129S6(Cg)-Tgfbr1tm1.1Hcd | J:204960 | View | ||||
Loeys-Dietz syndrome | Tgfbr2tm1.1Hcd/Tgfbr2+ | 129S6(Cg)-Tgfbr2tm1.1Hcd | J:204960 | View | ||||
lysosomal acid lipase deficiency | Lipatm1Ggb/Lipatm1Ggb | involves: 129P2/OlaHsd * CF-1 | J:49674 | View | ||||
maturity-onset diabetes of the young |
Ins1tm1Jja/Ins1tm1Jja Ins2tm1Jja/Ins2tm1Jja |
involves: 129S2/SvPas | J:40377, J:77595 | View | ||||
maturity-onset diabetes of the young | Ins2Akita/Ins2+ | C57BL/6-Ins2Akita | J:40063 | View | ||||
maturity-onset diabetes of the young | Ins2Akita/Ins2+ | C57BL/6-Ins2Akita/J | J:99412 | View | ||||
maturity-onset diabetes of the young | Mafatm1Staka/Mafatm1Staka | involves: ICR | J:99126 | View | ||||
maturity-onset diabetes of the young | Pdx1tm1Ted/Pdx1+ | involves: 129P2/OlaHsd | J:48516, J:82969 | View | ||||
maturity-onset diabetes of the young | Tgm2tm1Gml/Tgm2tm1Gml | involves: 129X1/SvJ * C57BL/6 | J:75566, J:78633, J:82489 | View | ||||
Meckel syndrome | bpck/bpck | B6C3Fe a/a-bpck/J | J:144929 | View | ||||
Meckel syndrome | Cc2d2atm1Asw/Cc2d2atm1Asw | Not Specified | J:226310 | View | ||||
Meckel syndrome | Cep55em1.1Hyli/Cep55em1.1Hyli | involves: C57BL/6 | J:313163 | View | ||||
Meckel syndrome | Mks1hlb614/Mks1hlb614 | involves: C3H * C57BL/6 | J:167534 | View | ||||
Meckel syndrome | Mks1krc/Mks1krc | involves: C3HeB/FeJ * C57BL/6 * CD-1 | J:154075 | View | ||||
Meckel syndrome | Mks1tm1a(EUCOMM)Wtsi/Mks1tm1a(EUCOMM)Wtsi | involves: C57BL/6 * C57BL/6N | J:196290 | View | ||||
Meckel syndrome | Rpgrip1ltm1Urt/Rpgrip1ltm1Urt | involves: 129S1/Sv * 129X1/SvJ | J:123018 | View | ||||
Meckel syndrome | Tbc1d32b2b2284Clo/Tbc1d32b2b2284Clo | C57BL/6J-Tbc1d32b2b2284Clo | J:175213 | View | ||||
Meckel syndrome | Tmem67tm1Dgen/Tmem67tm1Dgen | B6.129P2-Tmem67tm1Dgen | J:193837 | View | ||||
microvillus inclusion disease |
Cdc42tm1Brak/Cdc42tm1Brak Tg(Vil1-cre)997Gum/0 |
involves: C57BL/6J * SJL | J:184563 | View | ||||
Miller-Dieker lissencephaly syndrome |
Dph1tm1.1Cmch/Dph1tm1.1Cmch Edil3Tg(Sox2-cre)1Amc/Edil3+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * CBA | J:214744 | View | ||||
Miller-Dieker lissencephaly syndrome |
Dph1tm1.1Cmch/Dph1tm1.1Cmch H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * CBA/J | J:214744 | View | ||||
Miller-Dieker lissencephaly syndrome | Dph1tm2Bhr/Dph1tm2Bhr | involves: 129S4/SvJae * C57BL/6J | J:214744 | View | ||||
Miller-Dieker lissencephaly syndrome | Hic1tm1Sbb/Hic1tm1Sbb | involves: 129S4/SvJae * C57BL/6 | J:60589 | View | ||||
Miller-Dieker lissencephaly syndrome | Mnttm1.1Awb/Mnttm1.1Awb | involves: 129S6/SvEvTac * FVB/N | J:90397 | View | ||||
Miller-Dieker lissencephaly syndrome | Pafah1b1tm1Awb/Pafah1b1+ | involves: 129S6/SvEvTac * NIH Black Swiss | J:49531, J:59817 | View | ||||
Miller-Dieker lissencephaly syndrome |
Pafah1b1tm1Awb/Pafah1b1+ Ywhaetm1Awb/Ywhae+ |
either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss) | J:84075 | View | ||||
Miller-Dieker lissencephaly syndrome | Pafah1b1tm1Awb/Pafah1b1tm2Awb | involves: 129S6/SvEvTac * FVB/N * NIH Black Swiss | J:49531 | View | ||||
Miller-Dieker lissencephaly syndrome | Pafah1b1tm1Or/Pafah1b1+ | Not Specified | J:69631 | View | ||||
Miller-Dieker lissencephaly syndrome | Pafah1b1tm2.2Awb/Pafah1b1+ | involves: 129S6/SvEvTac * NIH Black Swiss | J:49531 | View | ||||
Miller-Dieker lissencephaly syndrome | Ywhaetm1Awb/Ywhaetm1Awb | either: 129S6/SvEvTac or (involves: 129S6/SvEvTac * NIH Black Swiss) | J:84075 | View | ||||
mitochondrial DNA depletion syndrome 3 | Mpv17/Mpv17 | CFW-Mpv17/J | J:143355 | View | ||||
Muir-Torre syndrome | Fhittm1Hbn/Fhit+ | involves: 129X1/SvJ * C57BL/6 | J:61946 | View | ||||
multiple synostoses syndrome | Fgf9tm1Zgwg/Fgf9+ | involves: 129S1/Sv | J:241783 | View | ||||
multiple synostoses syndrome | Fgf9tm1Zgwg/Fgf9tm1Zgwg | involves: 129S1/Sv | J:241783 | View | ||||
multiple synostoses syndrome | Gdf5Bp-5J/Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 | B4gat1m1Ddg/B4gat1tm1(KOMP)Vlcg | involves: C3H/He * C57BL/6 * C57BL/6NTac | J:194150 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 | Fkrptm1Itl/Fkrptm1Itl | involves: 129S6/SvEvTac * C57BL/6N | J:164448 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 | Fkrptm1Scbr/? | Not Specified | J:258757 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 | Fktntm1Ttd/Fktntm2(FCMD)Ttd | involves: 129S7/SvEvBrd | J:144746 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 |
Fktntm3.1Ttd/Fktntm3.1Ttd Myf5tm3(cre)Sor/Myf5+ |
involves: 129S4/SvJaeSor * C57BL/6 | J:198535 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 |
Fktntm3.1Ttd/Fktntm3.1Ttd Tg(Ckmm-cre)5Khn/0 |
involves: C57BL/6 * FVB | J:198535 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 | Large1m1Btlr/Large1m1Btlr | C57BL/6J-Large1m1Btlr | J:307652 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 | Large1myd/Large1myd | B6.Cg-Large1myd/Pjn | J:100214 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 | Large1vls/Large1vls | B6.CAST(Cg)-Large1vls/Pjn | J:100214 | View | ||||
muscular dystrophy-dystroglycanopathy type B1 | Pomgnt1tm1.1Cfg/Pomgnt1tm1.1Cfg | involves: C57BL/6 | J:258757 | View | ||||
myofibrillar myopathy 1 | Ldb3tm1Chen/Ldb3tm1Chen | involves: 129S1/Sv * 129X1/SvJ * Black Swiss | J:72799 | View | ||||
nail-patella syndrome |
Ldb1tm1Witz/Ldb1tm1Witz Tg(NPHS2-cre)295Lbh/0 |
involves: C57BL/6 * SJL | J:122505 | View | ||||
nephronophthisis |
Ahi1tm1Jgg/Ahi1+ Lrp6Gt(Ex187)Byg/Lrp6+ |
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ | J:154321 | View | ||||
nephronophthisis |
Ahi1tm1Jgg/Ahi1tm1Jgg Tg(TCF/Lef1-lacZ)34Efu/0 |
involves: 129S1/Sv * 129X1/SvJ | J:154321 | View | ||||
nephronophthisis | Cntrlb2b1468.1Clo/Cntrlb2b1468.1Clo | C57BL/6J-Cntrlb2b1468.1Clo | J:175213 | View | ||||
nephronophthisis | Sdccag8Gt(OST40418)Lex/Sdccag8Gt(OST40418)Lex | involves: 129S5/SvEvBrd * C57BL/6J | J:226661 | View | ||||
nephronophthisis | Wwtr1tm1Whun/Wwtr1tm1Whun | either: (involves: 129S6/SvEvTac) or (involves: 129S6/SvEvTac * C57BL/6) | J:119488 | View | ||||
neurodegeneration with brain iron accumulation 2a | gnd/gnd | C3H/HeJ-gnd | J:11718 | View | ||||
neurodegeneration with brain iron accumulation 2a | inad/inad | C57BL/6-inad | J:97670 | View | ||||
neurodegeneration with brain iron accumulation 2a | nad/nad | C(D2)-nad | J:156089 | View | ||||
neurogenic-type arthrogryposis multiplex congenita-2 | pma/pma | involves: CF-1 | J:8195 | View | ||||
neuronal ceroid lipofuscinosis 3 | Clcn3tm1Suc/Clcn3tm1Suc | involves: 129P2/OlaHsd * C57BL/6 | J:96311 | View | ||||
neuronal ceroid lipofuscinosis 3 | Clcn6tm1Tjj/Clcn6tm1Tjj | involves: 129S1/Sv * 129X1/SvJ | J:113752 | View | ||||
neuronal ceroid lipofuscinosis 3 | Ppt1tm1Hof/Ppt1tm1Hof | involves: 129S6/SvEvTac * C57BL/6J | J:72931 | View | ||||
non-syndromic X-linked intellectual disability | Dlg3tm1Grnt/Y | involves: 129P2/OlaHsd * C57BL/6J | J:238576 | View | ||||
non-syndromic X-linked intellectual disability | Iqsec2em1Csbg/Y | C57BL/6NHsd-Iqsec2em1Csbg | J:284750 | View | ||||
non-syndromic X-linked intellectual disability | Iqsec2em1Frk/Y | involves: C3HeB/FeJ * C57BL/6NJ | J:284762 | View | ||||
Noonan syndrome | Apaf1Gt(IRESBetageo)XIX18Pgr/Apaf1Gt(IRESBetageo)XIX18Pgr | involves: 129S1/Sv * 129X1/SvJ * NMRI | J:49840 | View | ||||
Noonan syndrome | Kat6bGt(pKC199)1Pgr/Kat6bGt(pKC199)1Pgr | involves: 129S2/SvPas | J:178264 | View | ||||
Noonan syndrome with multiple lentigines | Ptpn11tm1.1Ics/Ptpn11+ | involves: 129S2/SvPas * C57BL/6 * FVB/N | J:216593 | View | ||||
Noonan syndrome with multiple lentigines | Ptpn11tm4.2Bgn/Ptpn11+ | involves: 129S6/SvEvTac * C57BL/6J * FVB/N | J:172033 | View | ||||
Noonan syndrome with multiple lentigines | Tg(Myh7-Ptpn11*Q510E)#Krnz/0 | FVB/N-Tg(Myh7-Ptpn11*Q510E)#Krnz | J:222124 | View | ||||
Norrie disease | Fzd4tm1Nat/Fzd4tm1Nat | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:107732 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-Crc/Mitf+ | involves: CBA/CaCrc | J:83500 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-Crc/MitfMi-Crc | involves: CBA/CaCrc | J:83500 | View | ||||
ocular albinism with sensorineural deafness | Mitfmi-enu122/Mitf+ | involves: 102 * C3H | J:46254 | View | ||||
ocular albinism with sensorineural deafness | Mitfmi-enu122/Mitfmi-enu122 | involves: 102 * C3H | J:46254 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-H/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-H/MitfMi-H | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-H/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-wh/Mitf+ | involves: C57BL * DBA | J:13058 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-wh/MitfMi-wh | involves: C57BL * DBA | J:13058 | View | ||||
ocular albinism with sensorineural deafness | MitfMi-wh/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
ocular albinism with sensorineural deafness | Mitfmi-x/Mitfmi-x | involves: NZB/Mac | J:83501 | View | ||||
ocular albinism with sensorineural deafness | MitfMi/MitfMi | Not Specified | J:30758 | View | ||||
ocular albinism with sensorineural deafness | MitfRorp/Mitf+ | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
ocular albinism with sensorineural deafness | MitfRorp/MitfRorp | involves: BALB/cAnN * C3H/HeN | J:75964 | View | ||||
oculocutaneous albinism | Oca2p-6Btlr/Oca2p-6Btlr | C57BL/6J-Oca2p-6Btlr | J:215820 | View | ||||
oculocutaneous albinism | Slc45a2uw-6J/Slc45a2uw-6J | CAST/EiJ-Slc45a2uw-6J/GrsrJ | J:190732 | View | ||||
oculocutaneous albinism | Slc45a2uw-7J/Slc45a2uw-7J | C3H/HeJ-Slc45a2uw-7J/GrsrJ | J:190733 | View | ||||
oculocutaneous albinism | Slc45a2uw-bls/Slc45a2uw-bls | wild Corsican mouse | J:13805 | View | ||||
oculocutaneous albinism | Slc45a2uw-d/Slc45a2uw-d | involves: TF/Le | J:41299 | View | ||||
oculocutaneous albinism | Slc45a2Uw-dbr/Slc45a2+ | B10.PL-H2u/(73NS)Sn | J:41299 | View | ||||
oculocutaneous albinism | Slc45a2Uw-dbr/Slc45a2Uw-dbr | B10.PL-H2u/(73NS)Sn | J:41299 | View | ||||
oculocutaneous albinism | Slc45a2uw/Slc45a2uw | C57BL/6J-Slc45a2uw/J | J:41299 | View | ||||
osteogenesis imperfecta type 2 | Smpd3fro/Smpd3fro | Not Specified | J:3906 | View | ||||
osteogenesis imperfecta type 3 | Smpd3fro/Smpd3fro | Not Specified | J:3906 | View | ||||
osteogenesis imperfecta type 5 | SucoGt(KST050)Byg/SucoGt(KST050)Byg | involves: 129P2/OlaHsd * C57BL/6 * CD-1 | J:159823 | View | ||||
PCWH syndrome | Mpztm1Msch/Mpz+ | involves: 129S7/SvEvBrd * C57BL/6 | J:82432 | View | ||||
Pendred Syndrome | Foxi1tm1Sven/Foxi1tm1Sven | involves: CD-1 | J:83207 | View | ||||
Pierson syndrome | Tns2nph/Tns2nph | involves: ICR | J:108691 | View | ||||
polycystic liver disease | Ucp2tm1Lowl/Ucp2tm1Lowl | B6.129S4-Ucp2tm1Lowl | J:272325 | View | ||||
popliteal pterygium syndrome | Ripk4tm1Pmh/Ripk4tm1Pmh | involves: 129 * C57BL/6 | J:183160, J:191507 | View | ||||
primary ciliary dyskinesia | Ap1b1b2b1660Clo/Ap1b1b2b1660Clo | C57BL/6J-Ap1b1b2b1660Clo | J:175213 | View | ||||
primary ciliary dyskinesia | b2b227Clo/b2b227Clo | C57BL/6J-b2b227Clo | J:175213 | View | ||||
primary ciliary dyskinesia | b2b1146Clo/b2b1146Clo | C57BL/6J-b2b1146Clo | J:175213 | View | ||||
primary ciliary dyskinesia | b2b1200Clo/b2b1200Clo | C57BL/6J-b2b1200Clo | J:175213 | View | ||||
primary ciliary dyskinesia | b2b1700Clo/b2b1700Clo | C57BL/6J-b2b1700Clo | J:175213 | View | ||||
primary ciliary dyskinesia | b2b1929Clo/b2b1929Clo | C57BL/6J-b2b1929Clo | J:175213 | View | ||||
primary ciliary dyskinesia | b2b2059Clo/b2b2059Clo | C57BL/6J-b2b2059Clo | J:175213 | View | ||||
primary ciliary dyskinesia | b2b2350Clo/b2b2350Clo | C57BL/6J-b2b2350Clo | J:175213 | View | ||||
primary ciliary dyskinesia | Cby1tm1Ktkm/Cby1tm1Ktkm | B6.129-Cby1tm1Ktkm | J:147413, J:166685 | View | ||||
primary ciliary dyskinesia | Del(19Poll-Dcpd)1Nmt/Del(19Poll-Dcpd)1Nmt | involves: 129P2/OlaHsd | J:75779 | View | ||||
primary ciliary dyskinesia | Dnaaf5em1Slb/Dnaaf5em1Slb | C57BL/6-Dnaaf5em1Slb | J:342770 | View | ||||
primary ciliary dyskinesia | Dnah5b2b2451Clo/Dnah5b2b2451Clo | C57BL/6J-Dnah5b2b2451Clo | J:175213 | View | ||||
primary ciliary dyskinesia | Dnai2b2b3405Clo/Dnai2b2b3405Clo | C57BL/6J-Dnai2b2b3405Clo | J:175213 | View | ||||
primary ciliary dyskinesia | Dpcd/PollGt(OST280355)Lex/Dpcd/PollGt(OST280355)Lex | involves: 129S5/SvEvBrd * C57BL/6Brd | J:171184 | View | ||||
primary ciliary dyskinesia | Foxj1tm1Bph/Foxj1tm1Bph | involves: 129S1/Sv * 129X1/SvJ * Black Swiss | J:50025 | View | ||||
primary ciliary dyskinesia | Foxj1tm1Slb/Foxj1tm1Slb | involves: 129X1/SvJ | J:73616 | View | ||||
primary ciliary dyskinesia |
Gas2l2tm1c(KOMP)Wtsi/Gas2l2tm1c(KOMP)Wtsi Foxj1tm1.1(cre/ERT2/GFP)Htg/Foxj1+ |
involves: 129P2/OlaHsd * 129S4/SvJaeSor * C57BL/6N | J:277289 | View | ||||
primary ciliary dyskinesia | Gm572b2b1167Clo/Gm572b2b1167Clo | C57BL/6J-Gm572b2b1167Clo | J:175213 | View | ||||
primary ciliary dyskinesia | Pcsk5b2b1549Clo/Pcsk5b2b1549Clo | C57BL/6J-Pcsk5b2b1549Clo | J:175213 | View | ||||
primary ciliary dyskinesia | Slit2b2b1200.1Clo/Slit2b2b1200.1Clo | C57BL/6J-Slit2b2b1200.1Clo | J:175213 | View | ||||
primary ciliary dyskinesia | Spef2bgh/Spef2bgh | involves: 129S6/SvEvTac * C57BL/6J * C57BL/10J | J:176695 | View | ||||
primary ciliary dyskinesia | Spef2bgh/Spef2bgh | involves: C57BL/6J * C57BL/10J | J:176695 | View | ||||
primary ciliary dyskinesia | Ttll1tm1Seto/Ttll1tm1Seto | involves: 129S/SvEv * C57BL/6 | J:161297 | View | ||||
primary ciliary dyskinesia 14 | b2b2025Clo/b2b2025Clo | C57BL/6J-b2b2025Clo | J:175213 | View | ||||
progeria | Sirt6tm1Fwa/Sirt6tm1Fwa | involves: 129S6/SvEvTac * 129X1/SvJ | J:112817 | View | ||||
progeria | Vcpip1em1Zlou/Vcpip1em1Zlou | C57BL/6NHsd-Vcpip1em1Zlou | J:297179 | View | ||||
progeria | Zmpste24tm1Otin/Zmpste24tm1Otin | involves: 129P2/OlaHsd | J:164373 | View | ||||
progeria | Zmpste24tm1Sgy/Zmpste24tm1Sgy | B6.129S4-Zmpste24tm1Sgy | J:106706 | View | ||||
progeria | Zmpste24tm1Sgy/Zmpste24tm1Sgy | involves: 129S4/SvJae * C57BL/6 | J:95274 | View | ||||
pyridoxine-dependent epilepsy | Aldh7a1tm1d(EUCOMM)Hmgu/Aldh7a1tm1d(EUCOMM)Hmgu | B6(FVB)-Aldh7a1tm1d(EUCOMM)Hmgu | J:298561 | View | ||||
recessive dystrophic epidermolysis bullosa | Col7a1em#Jtol/Col7a1em#Jtol | involves: 129S4/SvJae * BALB/c * C57BL/Ka * NOD | J:280214 | View | ||||
recessive dystrophic epidermolysis bullosa | Col7a1tm1Lbt/Col7a1tm1Lbt | involves: 129S1/Sv * 129X1/SvJ * C57BL/6Crl | J:136145 | View | ||||
recessive dystrophic epidermolysis bullosa | Col7a1tm1Uit/Col7a1tm1Uit | involves: 129S1/Sv | J:155326 | View | ||||
recessive dystrophic epidermolysis bullosa | Col7a1tm1Uit/Col7a1tm1Uit | involves: 129S1/Sv * C57BL/6J | J:58533 | View | ||||
recessive dystrophic epidermolysis bullosa |
Col7a1tm1Uit/Col7a1tm1Uit Tg(KRT14-COL7A1*)1Shzu/0 |
involves: 129S1/Sv * C57BL/6 * DBA/2 | J:155326 | View | ||||
recessive dystrophic epidermolysis bullosa | Grip1tm1Paw/Grip1tm1Paw | involves: 129X1/SvJ * ICR | J:79476 | View | ||||
retinitis pigmentosa 2 | Tg(Rho-Arl3*Q71L)#Visu/0 | involves: 129 * FVB/N | J:235882 | View | ||||
right atrial isomerism | Acvr2btm1Enl/Acvr2btm1Enl | either: (involves: 129S4/SvJae) or (involves: 129S4/SvJae * C57BL/6J) | J:42018 | View | ||||
right atrial isomerism | Cfc1tm1Cbm/Cfc1tm1Cbm | Not Specified | J:58530 | View | ||||
right atrial isomerism | Cfc1tm1Mms/Cfc1tm1Mms | either: (involves: 129S6/SvEvTac * Black Swiss) or (involves: 129S6/SvEvTac * C57BL/6J) | J:58104 | View | ||||
Robinow syndrome | b2b3077Clo/b2b3077Clo | C57BL/6J-b2b3077Clo | J:175213 | View | ||||
Robinow syndrome | Dnaaf4b2b811.1Clo/Dnaaf4b2b811.1Clo | C57BL/6J-Dnaaf4b2b811.1Clo | J:175213 | View | ||||
Robinow syndrome | Wnt5ab2b3077.1Clo/Wnt5ab2b3077.1Clo | C57BL/6J-Wnt5ab2b3077.1Clo | J:175213 | View | ||||
sarcosinemia | sar/sar | BTBR-sar | J:37 | View | ||||
Seckel syndrome | Atrtm1Ofc/Atrtm1Ofc | Not Specified | J:151542 | View | ||||
Seckel syndrome |
Atriptm1.1Pof/Atriptm1.1Pof Tg(Pax6-cre,GFP)2Pgr/0 |
involves: 129P2/OlaHsd * C57BL/6 | J:297493 | View | ||||
Seckel syndrome | Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi | B6Brd;B6N-Tyrc-Brd Cenpjtm1a(EUCOMM)Wtsi/Wtsi | J:194085 | View | ||||
Seckel syndrome | Cep63Gt(EUCE0251h11)Hmgu/Cep63Gt(EUCE0251h11)Hmgu | involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6 | J:224364 | View | ||||
Senior-Loken syndrome | Tmem218Gt(OST40451)Lex/Tmem218Gt(OST40451)Lex | involves: 129S5/SvEvBrd * C57BL/6 | J:227399 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive | Prkdcscid/Prkdcscid | C.BKa-Prkdcscid | J:6958 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | Coro1akoy/Coro1akoy | C57BL/6-Coro1akoy | J:141431 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | Coro1aptcd/Coro1aptcd | B6.CTS-Coro1aptcd | J:141431 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | Coro1aptcd/Coro1atm1Achn | B6.Cg-Coro1aptcd Coro1atm1Achn | J:141431 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | Coro1atm1Achn/Coro1atm1Achn | B6.129X1-Coro1atm1Achn | J:141431 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | Jak3tm1Ljb/Jak3tm1Ljb | involves: 129S4/SvJae | J:64861 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive | Jak3tm1Tks/Jak3tm1Tks | involves: 129P2/OlaHsd * C57BL/6 | J:31231 | View | ||||
sickle cell anemia | Spta1sph-ha/Spta1sph-ha | either: (B6.D1-Spta1sph-ha x WB.D1-Spta1sph-ha)F1 or (WB.D1-Spta1sph-ha x B6.D1-Spta1sph-ha)F1 | J:12830 | View | ||||
Smith-McCort dysplasia | DymGt(GTR1.3)1Rul/DymGt(GTR1.3)1Rul | involves: 129 | J:141099 | View | ||||
SOST-related sclerosing bone dysplasia | Sosttm1(KOMP)Vlcg/Sosttm1(KOMP)Vlcg | involves: C57BL/6NTac | J:188586 | View | ||||
spinocerebellar ataxia type 27 | Fgf14tm1Dor/Fgf14tm1Dor | B6.129S6-Fgf14tm1Dor | J:134733 | View | ||||
split hand-foot malformation 1 | Dlx5/Dlx6tm1Levi/Dlx5/Dlx6tm1Levi | Not Specified | J:77244 | View | ||||
spondyloepiphyseal dysplasia congenita | Hapln1tm1Nid/Hapln1tm1Nid | involves: 129S1/Sv * 129X1/SvJ | J:52575 | View | ||||
Stargardt disease | Abca4tm1.1Rsmy/Abca4tm1.1Rsmy | involves: C57BL/6 | J:255529 | View | ||||
Stargardt disease | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae | J:141801 | View | ||||
Stargardt disease | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae * BALB/c | J:141801 | View | ||||
Stargardt disease | Abca4tm1Ght/Abca4tm1Ght | involves: 129S4/SvJae * C57BL/6 | J:56317 | View | ||||
Stargardt disease |
Abca4tm1Kpal/Abca4tm1Kpal Rdh8tm1Kpal/Rdh8tm1Kpal |
involves: 129 | J:213619 | View | ||||
Stargardt disease | Elovl4tm1Rayy/Elovl4+ | involves: 129 * C57BL/6J | J:114752 | View | ||||
Stargardt disease | Elovl4tm1Wked/Elovl4+ | involves: 129S/SvEv * 129S1/Sv | J:121481 | View | ||||
syndromic X-linked intellectual disability | Arxtm1.1Ics/Y | involves: 129S2/SvPas * C57BL/6J * C57BL/6N | J:262482 | View | ||||
syndromic X-linked intellectual disability | Rab39bem1Jfch/Y | C57BL/6N-Rab39bem1Jfch | J:287752 | View | ||||
thalassemia | Ppp1r15atm1.1Ajf/Ppp1r15atm1.1Ajf | involves: 129 * C57BL/6 | J:106905 | View | ||||
type 1 diabetes mellitus 2 |
Apobtm2Sgy/Apobtm2Sgy Ldlrtm1Her/Ldlrtm1Her Tg(Ins-Igf2)1Fbos/? |
involves: 129S7/SvEvBrd * C57BL/6 * C57BL/6J * SJL | J:227165 | View | ||||
type 1 diabetes mellitus 2 | Tg(Ins-Igf2)1Fbos/0 | involves: C57BL/6 * C57BLKs/J * SJL | J:141527 | View | ||||
type 1 diabetes mellitus 2 | Tg(Ins-Igf2)1Fbos/0 | involves: C57BL/6 * SJL | J:141527 | View | ||||
Usher syndrome type 2C | Slc4a7tm1Krtz/Slc4a7tm1Krtz | involves: 129S5/SvEvBrd * C57BL/6 | J:86635 | View | ||||
Usher syndrome type 3 |
Clrn1tm1.1Kuna/Clrn1tm1.1Kuna Tg(Atoh1-Clrn1)#Kuna/0 |
involves: C57BL/6J | J:255408 | View | ||||
Usher syndrome type 3 |
Clrn1tm2.1Kuna/Clrn1tm2.1Kuna Tg(Atoh1-Clrn1)#Kuna/0 |
involves: 129 * C57BL/6J | J:260239 | View | ||||
Waardenburg syndrome | Aebp2Gt(BC0681)Wtsi/Aebp2+ | involves: 129P2/OlaHsd * C57BL/6 | J:177673 | View | ||||
Waardenburg syndrome | Snai2tm2Grid/Snai2tm2Grid | involves: 129S1/Sv | J:80529 | View | ||||
Waardenburg syndrome type 1 | MitfMi-Crc/Mitf+ | involves: CBA/CaCrc | J:83500 | View | ||||
Walker-Warburg syndrome | Col4a1deltaex40/Col4a1+ | involves: 129S/SvEv * C57BL/6J | J:172720 | View | ||||
Williams-Beuren syndrome | b2b370Clo/b2b370Clo | C57BL/6J-b2b370Clo | J:175213 | View | ||||
Williams-Beuren syndrome | Baz1bMommeD10/Baz1b+ | involves: FVB/N | J:142335 | View | ||||
Williams-Beuren syndrome | Baz1bMommeD10/Baz1bMommeD10 | involves: FVB/N | J:142335 | View | ||||
Williams-Beuren syndrome | Baz1btm1Ska/Baz1b+ | involves: C57BL/6 * CBA | J:149990 | View | ||||
Williams-Beuren syndrome | Baz1btm1Ska/Baz1btm1Ska | involves: C57BL/6 * CBA | J:149990 | View | ||||
Williams-Beuren syndrome | Clip2tm1.1Gal/Clip2+ | involves: 129P2/OlaHsd * C57BL/6 | J:78711 | View | ||||
Williams-Beuren syndrome | Dlg4tm2.1Grnt/Dlg4tm2.1Grnt | involves: 129P2/OlaHsd * C57BL/6J | J:175436 | View | ||||
Williams-Beuren syndrome | Fzd9tm1Sjp/Fzd9tm1Sjp | involves: C57BL/6J | J:99893 | View | ||||
Williams-Beuren syndrome | Fzd9tm1Uta/Fzd9+ | involves: 129X1/SvJ | J:169924 | View | ||||
Williams-Beuren syndrome | Gtf2iGt(XE029)Byg/Gtf2i+ | involves: 129P2/OlaHsd * C57BL/6 | J:143508 | View | ||||
Williams-Beuren syndrome | Gtf2itm1Vcam/Gtf2itm1Vcam | involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:204278 | View | ||||
Williams-Beuren syndrome | Gtf2ird1Gt(XE465)Byg/Gtf2ird1+ | involves: 129P2/OlaHsd * C57BL/6 | J:143508 | View | ||||
Williams-Beuren syndrome | Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1Tg(Alb1-Myc)166.8Sst | involves: C57BL/6 * CBA | J:102709 | View | ||||
Williams-Beuren syndrome | Gtf2ird1Tg(Alb1-Myc)166.8Sst/Gtf2ird1Tg(Alb1-Myc)166.8Sst | involves: C57BL/6J * CBA/J | J:190478 | View | ||||
Williams-Beuren syndrome | Gtf2ird1tm1Hrd/Gtf2ird1tm1Hrd | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:182346 | View | ||||
Williams-Beuren syndrome | Limk1tm1Zpj/Limk1tm1Zpj | involves: 129 | J:86283 | View | ||||
Williams-Beuren syndrome | Loxb2b370.2Clo/Loxb2b370.2Clo | C57BL/6J-Loxb2b370.2Clo | J:175213 | View | ||||
Williams-Beuren syndrome | Srcinl/Srcinl | involves: 129 | J:229610 | View | ||||
Wiskott-Aldrich syndrome | Foxp3sf/Y | involves: 101/H * C3H/HeH * STOCK MR | J:10398 | View | ||||
Wiskott-Aldrich syndrome | Washc4em1Ssod/Washc4em1Ssod | involves: C57BL/6J * SJL/J | J:303795 | View | ||||
X-linked agammaglobulinemia | Pik3r1tm1Dfr/Pik3r1tm1Dfr | involves: 129S6/SvEvTac * C57BL/6 | J:52229, J:65523 | View | ||||
X-linked agammaglobulinemia | Pik3r1tm1Tka/Pik3r1tm1Tka | involves: C57BL/6 * CBA | J:52228 | View | ||||
X-linked chondrodysplasia punctata 1 | EbpTd/Ebp+ | Not Specified | J:55860 | View | ||||
X-linked chondrodysplasia punctata 1 | NsdhlBpa-1H/Nsdhl+ | involves: 101/H * C3H/HeH | J:7012 | View | ||||
X-linked dilated cardiomyopathy | Xlch/? | C57BL/6J-Xlch | J:136798 | View | ||||
X-linked dilated cardiomyopathy | Xlch/Xlch+ | involves: C3H/HeJ * C57BL/6J | J:136798 | View | ||||
xeroderma pigmentosum | Tg(KRT5-Terf2)PMBlas/Y | involves: C57BL/6 * CBA | J:102653 | View | ||||
xeroderma pigmentosum | Tg(KRT5-Terf2)POBlas/0 | involves: C57BL/6 * CBA | J:102653 | View | ||||
XFE progeroid syndrome | Ercc1tm1Jhjh/Ercc1tm1Jhjh | involves: 129P2/OlaHsd * C57BL/6 * FVB | J:117488 | View | ||||
Zellweger syndrome | Pex1tm1.1Hrw/Pex1tm1.1Hrw | involves: C57BL/6NTac | J:278655 | View | ||||
Zellweger syndrome | Pex1tm1.1Sjms/Pex1tm1.1Sjms | involves: 129 * C57BL/6N | J:210296 | View | ||||
Zellweger syndrome | Pex11btm1Sjg/Pex11b+ | B6.129-Pex11btm1Sjg | J:180632 | View | ||||
Zellweger syndrome | Pex11btm1Sjg/Pex11btm1Sjg | B6.129-Pex11btm1Sjg | J:180632 | View | ||||
Zellweger syndrome | Pex11btm1Sjg/Pex11btm1Sjg | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:76782 | View | ||||
![]() | age related macular degeneration 1 | Apoetm3(APOE*4)Mae/Apoetm3(APOE*4)Mae | involves: 129P2/OlaHsd * C57BL/6 | J:101147 | View | |||
age related macular degeneration 2 |
Abca4tm1Ght/Abca4tm1Ght Rdh8tm1Kpal/Rdh8tm1Kpal |
involves: 129 * 129S4/SvJae | J:154536 | View | ||||
alpha thalassemia | Hbab2(th)/Hba+ | either: (involves: 101 * SEC) or (involves: 101 * C57BL * SEC) | J:123943 | View | ||||
alpha thalassemia | Hbab2(th)/Hba+ | involves: C57BL/6J * SEC | J:32654 | View | ||||
alpha thalassemia | Hbab2(th)/Hba+ | SEC-Hbab2(th) | J:6452 | View | ||||
alpha thalassemia | Hbab3(th)/Hba+ | either: (involves: 101 * SEC) or (involves: 101 * C57BL * SEC) | J:123943 | View | ||||
alpha thalassemia | Hbab3(th)/Hba+ | involves: C57BL/6J * SEC | J:32654 | View | ||||
alpha thalassemia | Hbab3(th)/Hba+ | SEC-Hbab3(th) | J:6452 | View | ||||
alpha thalassemia | Hbath-J/Hba+ | involves: C57BL/6J | J:45721, J:32654 | View | ||||
Alzheimer's disease 4 |
Psen1tm1Jzt/Psen1tm1Jzt Psen2tm1Ber/Psen2tm1Ber Tg(Camk2a-cre)T29-1Stl/0 |
involves: C57BL/6 * CBA | J:90685 | View | ||||
congenital secretory sodium diarrhea 3 |
Prss8em1Bug/Prss8em1Bug Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg |
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * NIH Black Swiss | J:261068 | View | ||||
Dent disease |
Inpp5btm1Nbm/Inpp5btm1Nbm Ocrltm1Nbm/Ocrltm1Nbm Tg(INPP5B)CNbm/0 |
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N | J:185879 | View | ||||
Dent disease |
Inpp5btm1Nbm/Inpp5btm1Nbm Ocrltm1Nbm/Y Tg(INPP5B)CNbm/0 |
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N | J:185879 | View | ||||
dilated cardiomyopathy 1E | Scn5atm1(SCN5A)Rdn/Scn5atm3(SCN5A*)Rdn | involves: 129S6/SvEvTac | J:189389 | View | ||||
dilated cardiomyopathy 1E | Scn5atm3(SCN5A*)Rdn/Scn5atm3(SCN5A*)Rdn | involves: 129S6/SvEvTac | J:189389 | View | ||||
dilated cardiomyopathy 1P | Tg(Myh6-Pln*R9C)#Ces/0 | involves: FVB/N | J:82353 | View | ||||
Duchenne muscular dystrophy |
Itga7tm1Burk/Itga7tm1Burk Sspntm1Kcam/Sspntm1Kcam |
involves: 129S1/Sv * 129X1/SvJ | J:187752 | View | ||||
familial erythrocytosis 1 | Eportm1.4Jtp/Epor+ | involves: 129P2/OlaHsd * C57BL/6 | J:67205 | View | ||||
familial erythrocytosis 1 | Eportm1.4Jtp/Eportm1.4Jtp | involves: 129P2/OlaHsd * C57BL/6 | J:67205 | View | ||||
Griscelli syndrome type 2 |
a/a Rab27aash/Rab27aash |
involves: C3H/HeSnJ * C57BL/6J | J:77395 | View | ||||
hereditary breast ovarian cancer syndrome |
Brca1tm1Cxd/Brca1tm2Cxd Trp53tm1Brd/Trp53+ Tg(MMTV-cre)4Mam/0 |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * Black Swiss * FVB | J:54533 | View | ||||
hereditary breast ovarian cancer syndrome |
Brca1tm2Cxd/Brca1tm2Cxd Tg(MMTV-cre)4Mam/0 Tg(MMTV-rtTA)1Lach/0 Tg(tetO-Esr1)#Paf/0 Trp53tm1Brd/Trp53+ |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB | J:132088 | View | ||||
hereditary breast ovarian cancer syndrome |
Brca1tm2Cxd/Brca1tm2Cxd Trp53tm1Brd/Trp53+ Tg(MMTV-cre)4Mam/0 |
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 * FVB | J:132088 | View | ||||
hereditary sensory and autonomic neuropathy type 5 | Ngftm1(NGF*)Cat/Ngf+ | involves: 129S1/Sv * 129X1/SvJ | J:282017 | View | ||||
hereditary sensory and autonomic neuropathy type 5 | Ngftm1(NGF*)Cat/Ngftm1(NGF*)Cat | involves: 129S1/Sv * 129X1/SvJ | J:284096 | View | ||||
intermediate spinal muscular atrophy | Smn1tm5(Smn1/SMN2)Mrph/Smn1tm5(Smn1/SMN2)Mrph | involves: 129S6/SvEvTac * C57BL/6J * C57BL/6NTac | J:186987 | View | ||||
Kennedy's disease | Artm4(AR)Dmr/Y | involves: 129S1/Sv * C57BL/6J | J:104360, J:114552 | View | ||||
Machado-Joseph disease | Atxn3tm2.1(ATXN3*)Mfig/Atxn3+ | involves: 129 * C57BL/6J | J:218541 | View | ||||
mitochondrial DNA depletion syndrome 1 |
Tymptm1Mihi/Tymptm1Mihi Upp1tm1Gp/Upp1tm1Gp |
involves: 129 * 129X1/SvJ * C57BL/6J | J:144245 | View | ||||
oculocerebrorenal syndrome |
Inpp5btm1Nbm/Inpp5btm1Nbm Ocrltm1Nbm/Ocrltm1Nbm Tg(INPP5B)CNbm/0 |
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N | J:185879 | View | ||||
oculocerebrorenal syndrome |
Inpp5btm1Nbm/Inpp5btm1Nbm Ocrltm1Nbm/Y Tg(INPP5B)CNbm/0 |
involves: 129S/SvEv * 129S6/SvEvTac * FVB/N | J:185879 | View | ||||
pachyonychia congenita |
Krt17tm1Cou/Krt17tm1Cou Krt6a/Krt6btm1Cou/Krt6a/Krt6btm1Cou Krt6a/Krt6btm1Cou/Krt6a/Krt6btm1Cou |
involves: 129S2/SvPas * C57BL/6 | J:95390 | View | ||||
progressive familial intrahepatic cholestasis 4 |
Tjp1tm1.1Whun/Tjp1tm1.1Whun Tjp2tm2Whun/Tjp2tm2Whun Speer6-ps1Tg(Alb-cre)21Mgn/Speer6-ps1+ |
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6N * C57BL/6NTac * DBA/2 | J:306936 | View | ||||
sickle cell anemia |
Hbatm1(HBA)Tow/Hbatm1(HBA)Tow Hbbtm2(HBG1,HBB*)Tow/Hbbtm2(HBG1,HBB*)Tow |
Not Specified | J:134980 | View | ||||
sickle cell anemia |
Hbatm1(HBA)Tow/Hbatm1(HBA)Tow Hbbtm2(HBG1,HBB*)Tow/Hbbtm2(HBG1,HBB*)Tow Slc12a4Rbc10/Slc12a4+ |
involves: 129 * BALB/c * C57BL/6J | J:227339 | View | ||||
sickle cell anemia |
Hbatm1Paz/Hbatm1Paz Hbbtm1Tow/Hbbtm1Tow Tg(HBA-HBBs)41Paz/? |
involves: 129S2/SvPas * 129S7/SvEvBrd * Black Swiss * C57BL/6 * DBA/2* FVB/N | J:44161 | View | ||||
sickle cell anemia |
Hbbd3th/Hbb+ Tg(HBB-AR-HBA2,-HBB*)58Rub/0 Tg(LCR-HBA2,LCR-HBB)11Cos/0 |
involves: FVB/N * Swiss Webster | J:94190 | View | ||||
sickle cell anemia |
Hbbd3th/Hbb+ Tg(LCR-HBA1,LCR-HBB*)1Tow/0 |
involves: C57BL/6 * DBA/2J * SJL | J:127701 | View | ||||
sickle cell anemia |
Hbbd3th/Hbb+ Tg(LCR-HBA2,LCR-HBB*)1Cos/0 |
involves: C57BL/6J * CBA/J * DBA/2J | J:94193 | View | ||||
sickle cell anemia |
Hbbd3th/Hbbd3th Tg(HBB-AR-HBA2,-HBB*)58Rub/0 Tg(LCR-HBA2,LCR-HBB)11Cos/0 |
involves: FVB/N * Swiss Webster | J:94190 | View | ||||
Sjogren-Larsson syndrome |
Aldh3a2tm1a(EUCOMM)Wtsi/Aldh3a2tm1a(EUCOMM)Wtsi Aldh3b2em1Akih/Aldh3b2em1Akih |
involves: C57BL/6J * C57BL/6N | J:330263 | View | ||||
Sotos syndrome | Del(13Simc1-B4galt7)2Dja/+ | involves: 129P2/OlaHsd * 129S7/SvEvBrd * C57BL/6J | J:190741 | View | ||||
spinocerebellar ataxia type 15 |
Glatm1Kul/Glatm1Kul Itpr1wblo/Itpr1wblo |
B6;129-Glatm1Kul Itpr1wblo/GrsrJ | J:222308 | View | ||||
spinocerebellar ataxia type 15 |
Glatm1Kul/Y Itpr1wblo/Itpr1wblo |
B6;129-Glatm1Kul Itpr1wblo/GrsrJ | J:222308 | View | ||||
syndromic X-linked intellectual disability Lubs type | Mapttm1(Mecp2)Jae/Mapttm1(Mecp2)Jae | B6.Cg-Mapttm1(Mecp2)Jae | J:182685 | View | ||||
Wolfram syndrome 2 | Cisd2tm1Tfts/Cisd2tm1Tfts | B6.129S7-Cisd2tm1Tfts | J:148467 | View | ||||
Transgenes and Other Mutations | abdominal obesity-metabolic syndrome | Tg(RP11-578M14)5Mkru/0 | involves: FVB/N | J:256501 | View | |||
abdominal obesity-metabolic syndrome 1 | Tg(Fabp4-ENPP1)#Naba/0 | involves: C57BL/6J | J:182179 | View | ||||
abdominal obesity-metabolic syndrome 1 | Tg(Fabp4-Hsd11b1)7Jesf/0 | FVB-Tg(Fabp4-Hsd11b1)7Jesf | J:107046 | View | ||||
adult-onset autosomal dominant demyelinating leukodystrophy | Tg(Plp1-LMNB1)1108Qsp/0 | involves: FVB/N | J:226169 | View | ||||
adult-onset autosomal dominant demyelinating leukodystrophy | Tg(Plp1-Lmnb1)#Yfu/0 | involves: FVB | J:197168 | View | ||||
advanced sleep phase syndrome 1 | Tg(PER2*S662G)867Ljp/0 | involves: C57BL/6 | J:126404 | View | ||||
advanced sleep phase syndrome 2 | Tg(CSNK1D*,-EGFP)816Yfu/? | involves: C57BL/6 * SJL | J:97658 | View | ||||
advanced sleep phase syndrome 2 | Tg(CSNK1D*,-EGFP)827Yfu/? | involves: C57BL/6 * SJL | J:97658 | View | ||||
age related macular degeneration 1 | Tg(APOB)1102Sgy/? | B6.Cg-Tg(APOB)1102Sgy | J:151253 | View | ||||
Alexander disease | Tg(GFAP)7Mes/0 | involves: FVB/N | J:99256 | View | ||||
Alexander disease | Tg(GFAP)10Mes/0 | involves: FVB/N | J:99256 | View | ||||
Alexander disease | Tg(Gfap-GFAP*R239H)60TMIke/0 | involves: C57BL/6J | J:139349, J:138318 | View | ||||
alpha thalassemia | Hbatm1Ney/Hbatm1Ney | either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ) | J:86682 | 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(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0 |
involves: 129S1/Sv * 129X1/SvJ * C3H/HeJ * C57BL/6J | J:123534 | 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 | B6;C3-Tg(APPswe,PSEN1dE9)85Dbo/Mmjax | J:113199 | 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(APPSwFlLon,PSEN1*M146L*L286V)6799Vas/0 | involves: C57BL/6 * SJL | J:112949 | View | ||||
Alzheimer's disease 3 | Tg(PSEN1dE9)S9Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:104147 | View | ||||
Alzheimer's disease 3 | Tg(PSEN1H163R)G9Btla/0 | involves: 129S4/SvJae | J:58050 | View | ||||
Alzheimer's disease 4 | Tg(APP695)3Dbo/0 | B6.C3-Tg(APP695)3Dbo | J:109847 | View | ||||
Alzheimer's disease 4 |
Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0 |
involves: C3H/HeJ * C57BL/6J | J:43788 | View | ||||
Alzheimer's disease 4 |
Tg(APP695)3Dbo/0 Tg(PSEN1dE9)S9Dbo/0 |
involves: C3H/HeJ * C57BL/6J | J:123534 | View | ||||
amyotrophic lateral sclerosis type 1 |
Cybbtm1Din/Y Tg(SOD1*G93A)dl1Gur/0 |
B6.Cg-Cybbtm1Din Tg(SOD1*G93A)dl1Gur | J:111782 | View | ||||
amyotrophic lateral sclerosis type 1 |
Isl1tm1(cre)Tmj/Isl1+ Tg(SOD1*G37R)1Dwc/0 |
involves: 129X1/SvJ * C57BL/6 | J:109131 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(ITGAM-cre)2781Gkl/0 Tg(SOD1*G37R)1Dwc/0 |
involves: C57BL/6 * CBA | J:109131 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Myl1-SOD1*G93A)#Amu/0 | FVB/NJ-Tg(Myl1-SOD1*G93A)#Amu | J:143747 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(NEFH)200Jpj/0 | Not Specified | J:69180 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(NEFH)200Jpj/Tg(NEFH)200Jpj | Not Specified | J:69180 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(NFH)120Jpj/0 | Not Specified | J:69180 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(NFH)120Jpj/Tg(NFH)120Jpj | Not Specified | J:69180 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Prnp-Immt/SOD1*G93A)7Gmnf/Tg(Prnp-Immt/SOD1*G93A)7Gmnf | involves: C57BL/6 * CBA * SJL | J:177846 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo/Tg(Prnp-SOD1*G37R,-PSEN1)110Dbo | involves: C3H * C57BL/6 | J:104655 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*)D-14Dbo/0 |
involves: C3H/HeJ * C57BL/6 * C57BL/6J * SJL | J:218091 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*G85R)#Roos/0 |
involves: C57BL/6 * C57BL/6J * SJL | J:147156 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*G93A)1Gur/0 |
involves: C57BL/6 * SJL | J:109458 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*L126Z)#Deng/0 |
involves: C57BL/6 * SJL | J:109458 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*)125Dbo/? | involves: C3H/HeJ * C57BL/6J | J:86421 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*)D-14Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:218091 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*)DF7Yaw/0 | C57BL/6-Tg(SOD1*)DF7Yaw | J:97932 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*)DF7Yaw/Tg(SOD1*)DF7Yaw | C57BL/6-Tg(SOD1*)DF7Yaw | J:97932 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G37R)9Dpr/0 | involves: C3H/HeJ * C57BL/6J | J:69178 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G37R)29Dpr/0 | involves: C3H/HeJ * C57BL/6J | J:69178, J:119631 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G37R)42Dpr/0 | involves: C3H/HeJ * C57BL/6J | J:69178 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G37R)106Dpr/0 | involves: C3H/HeJ * C57BL/6J | J:69178 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R)74Dwc/? | Not Specified | J:77600 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R)148Dwc/? | Not Specified | J:77600 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R)#Roos/0 | involves: C57BL/6J | J:147156 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R/EYFP)641Alho/Tg(SOD1*G85R/EYFP)641Alho | involves: C57BL/6J * SJL/J | J:144475 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G85R/EYFP)737Alho/Tg(SOD1*G85R/EYFP)737Alho | involves: C57BL/6J * SJL/J | J:212250 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | B6.Cg-Tg(SOD1*G93A)1Gur | J:155140 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | B6.Cg-Tg(SOD1*G93A)1Gur/J | J:211734 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | B6SJL-Tg(SOD1*G93A)1Gur | J:144199 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | B6SJL-Tg(SOD1*G93A)1Gur/J | J:133155, J:143173, J:146652, J:212250 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)1Gur/0 | involves: C57BL/6 * SJL | J:76718, J:91800, J:109458, J:130581 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)2Gur/0 | involves: C57BL/6 * SJL | J:32665, J:78629, J:89928 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G93A)dl1Gur/0 | involves: C57BL/6 * SJL | J:106420 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*G127X)716Mrkl/Tg(SOD1*G127X)716Mrkl | B6JBom.Cg-Tg(SOD1*G127X)716Mrkl | J:175594 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R)#Maw/0 | involves: C57BL/6 * DBA/2 | J:99701 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R)IAra/0 | involves: C57BL/6 * DBA/2 | J:221350 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R)LAra/0 | involves: C57BL/6 * DBA/2 | J:221350 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R*H48Q)58Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:119631 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*H46R*H48Q)139Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:119631 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*L126Z)45Dbo/0 | involves: C3H/HeJ * C57BL/6J | J:219482 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(SOD1*L126Z)#Deng/0 | involves: C57BL/6 * SJL | J:109458 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Thy1-DCTN1*G59S)M2Pcw/? | involves: C57BL/6 * SJL | J:132857 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(Thy1-SOD1*G93A)T1Hgrd/0 Tg(Thy1-SOD1*G93A)T3Hgrd/0 |
involves: C57BL/6 * CBA * FVB | J:134095 | View | ||||
amyotrophic lateral sclerosis type 1 | Tg(Thy1-SOD1*G93A)T3Hgrd/Tg(Thy1-SOD1*G93A)T3Hgrd | involves: C57BL/6 * CBA * FVB | J:134095 | View | ||||
arrhythmogenic right ventricular dysplasia 9 | Tg(Myh6-Pkp2*/mRuby)4Rbrug/0 | involves: C57BL/6 * DBA/2 | J:237859 | View | ||||
arrhythmogenic right ventricular dysplasia 9 |
Tg(Myh6-Pkp2*/mRuby)4Rbrug/0 Tg(Myh6-Pkp2*/mRuby)5Rbrug/0 |
involves: C57BL/6 * DBA/2 | J:237859 | View | ||||
arrhythmogenic right ventricular dysplasia 9 | Tg(Myh6-Pkp2*/mRuby)5Rbrug/0 | involves: C57BL/6 * DBA/2 | J:237859 | View | ||||
arrhythmogenic right ventricular dysplasia 12 | Tg(Myh6-JUP*)1Dpju/0 | FVB/N-Tg(Myh6-JUP*)1Dpju | J:235770 | View | ||||
autosomal dominant hypophosphatemic rickets | Tg(APOE-FGF23*R176Q)#Ack/0 | involves: C57BL/6J * CBA | J:93981 | 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 limb-girdle muscular dystrophy type 1 | Tg(Ckm-DNAJB6_ib*F93L)#Ccwe/0 | B6.Cg-Tg(Ckm-DNAJB6_ib*F93L)#Ccwe | J:226488 | View | ||||
autosomal recessive hypophosphatemic rickets | Tg(APOE-FGF23*R176Q)#Ack/0 | involves: C57BL/6J * CBA | J:192371 | View | ||||
autosomal recessive nonsyndromic deafness 38 | Phl1101/H/Phl1101/H | involves: 101/H * MAI/Pas | J:111682 | View | ||||
autosomal recessive nonsyndromic deafness 38 | Phl1101/H/Phl1101/H | involves: 101/H * MBT/Pas | J:111682 | View | ||||
autosomal recessive polycystic kidney disease | T(2;10)67Gso/T(2;10)67Gso | involves: 101 * C3H * C3H/Rl * C57BL/RlGso * SEC/RlGso | J:75799 | 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 | ||||
beta thalassemia | Hbbtm1Unc/Hbbtm1Unc | involves: 129P2/OlaHsd * C57BL/6J | J:4932 | View | ||||
beta thalassemia | Rr320tm1.1Mkg/Rr320+ | involves: 129 | J:60714 | View | ||||
beta thalassemia | Rr320tm2Mkg/Rr320tm2Mkg | involves: 129S4/SvJaeSor | J:28981 | View | ||||
CADASIL 1 | Tg(Notch3*R169C)88Bbb/0 | involves: FVB/N | J:220006 | View | ||||
Carney complex |
Tg(CMV-tTA)3Bjd/0 Tg(tetO-Prkar1a*x2as)1Stra/0 |
involves: C57BL/6 * NMRI * SJL | J:95465 | View | ||||
cataract | Tg(Cryaa-APEH)KKS4Kksha/0 | FVB/N-Tg(Cryaa-APEH)KKS4Kksha | J:212432 | View | ||||
cataract 2 multiple types | Tg(CRYBB1-CRYGC*)#Jfhe/? | involves: FVB/N | J:181433 | View | ||||
Charcot-Marie-Tooth disease axonal type 2F | Tg(Thy1-HSPB1*S135F)#Lvdb/0 | involves: FVB/N | J:174508 | 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)C22Clh/0 | involves: C57BL/6J * CBA/Ca | J:78221, J:76795 | View | ||||
Charcot-Marie-Tooth disease type 1A | Tg(PMP22)C61Clh/0 | B6.Cg-Tg(PMP22)C61Clh | J:158350 | 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 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 2E | Tg(NEFL*E397K)#Milg/0 | Not Specified | J:173771 | 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 | ||||
cone-rod dystrophy 6 | Tg(Rho-GUCY2D*R838S)362Amd/0 | involves: C57BL/6 * C57BL/6J * SJL | J:237633 | View | ||||
cone-rod dystrophy 6 | Tg(Rho-GUCY2D*R838S)379Amd/0 | involves: C57BL/6 * C57BL/6J * SJL | J:237633 | View | ||||
cone-rod dystrophy 14 | Tg(Rho-GUCA1A*Y99C)L53Amd/0 | involves: C57BL/6 * DBA/2 | J:180234 | View | ||||
congenital generalized lipodystrophy type 2 | Tg(aP2-SREBF1c)9884Reh/0 | involves: C57BL/6J * SJL | J:50770 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(ATN1*)Q129Stsu/0 | involves: 129S/SvEv * C57BL/6J | J:144379 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(Eno2-ATN1)3Tx/Tg(Eno2-ATN1)3Tx | B6.Cg-Tg(Eno2-ATN1)3Tx | J:112706 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(Eno2-ATN1)14Tx/0 | B6.Cg-Tg(Eno2-ATN1)14Tx | J:112706 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(Prnp-ATN1)124Dbo/? | involves: C3H * C57BL/6 | J:70362 | View | ||||
dentatorubral-pallidoluysian atrophy | Tg(Prnp-ATN1)150Dbo/? | involves: C3H * C57BL/6 | J:70362 | View | ||||
DiGeorge syndrome | Del(16Es2el-Ufd1l)217Bld/+ | involves: 129S7/SvEvBrd * C57BL/6 | J:57757 | View | ||||
dilated cardiomyopathy 1A | Tg(Myh6-LMNA*E82K)35Lizh/0 | involves: C57BL/6J | J:167734 | View | ||||
dilated cardiomyopathy 1C | Tg(Myh6-LDB3*S196L)93Mva/0 | involves: C57BL/6J | J:243711 | 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 1E |
Tg(Myh6-rtTA)8585Jam/0 Tg(Myh6*/tetO-SCN5A*F1759A)#Marx/0 |
involves: C57BL/6 * CBA * FVB/NTac | J:229825 | View | ||||
dilated cardiomyopathy 1L | Tg(Myh6-Sgcd*S151A)5Mcn/0 | involves: 129T2/SvEms * C57BL/6J | J:117855 | View | ||||
dilated cardiomyopathy 1P | Tg(Myh6-Pln*)#Egk/0 | Not Specified | J:105976 | 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 | ||||
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 | ||||
Feingold syndrome | Mirc1tm1.2Tyj/Mirc1+ | involves: 129S4/SvJae * C57BL/6 | J:188762 | View | ||||
fibrodysplasia ossificans progressiva | Tg(CAG-LacZ,-ACVR1*,-EGFP)35-1Mis/0 | involves: C57BL/6 * DBA/2 | J:142253 | View | ||||
Finnish type amyloidosis | Tg(Ckm-GSN*D187N)AJewe/0 | C57BL/6J-Tg(Ckm-GSN*D187N)AJewe | J:150825 | View | ||||
Finnish type amyloidosis | Tg(Ckm-GSN*D187N)AJewe/Tg(Ckm-GSN*D187N)AJewe | C57BL/6J-Tg(Ckm-GSN*D187N)AJewe | J:150825 | View | ||||
fragile X-associated tremor/ataxia syndrome |
Tg(Hnrnpa2b1-rtTA2S*M2)9Jstr/0 Tg(tetO-FMR1*,-EGFP)#Rkhu/0 |
involves: C57BL/6JRj * FVB/N | J:229379 | View | ||||
fragile X-associated tremor/ataxia syndrome | Tg(Pcp2-FMR1*)1Dln/0 | C57BL/6-Tg(Pcp2-Fmr1*)1Dln | J:149320 | View | ||||
fragile X-associated tremor/ataxia syndrome |
Tg(Prnp-rtTA2S*M2)#Rkhu/0 Tg(tetO-FMR1*,-EGFP)#Rkhu/0 |
involves: C57BL/6JRj | J:224760 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Prnp-TARDBP)3cPtrc/Tg(Prnp-TARDBP)3cPtrc | C57BL/6-Tg(Prnp-TARDBP)3cPtrc | J:163231 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(TARDBP)#Jpj/0 | involves: C3H * C57BL/6 | J:195184 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(TARDBP*A315T)#Jpj/0 | involves: C3H * C57BL/6 | J:195184 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(TARDBP*G348C)#Jpj/0 | involves: C3H * C57BL/6 | J:195184 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Thy1-TARDBP*)BOddo/0 | C57BL/6-Tg(Thy1-TARDBP*)BOddo | J:180165 | View | ||||
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Thy1-TARDBP*)BOddo/Tg(Thy1-TARDBP*)BOddo | C57BL/6-Tg(Thy1-TARDBP*)BOddo | J:223932 | 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 | ||||
Kennedy's disease | Tg(ACTA1-Ar)141Kyjo/0 | Not Specified | J:127205 | View | ||||
Kennedy's disease | Tg(AR*100Q)#Als/0 | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:170487 | View | ||||
Kennedy's disease | Tg(AR*100Q)C25Als/0 | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:89772 | View | ||||
Kennedy's disease | Tg(AR*100Q)C32Als/0 | involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:89772 | View | ||||
Kennedy's disease | Tg(CAG-AR*97Q)7-8Sobue/? | involves: C57BL/6 * C57BL/6J * DBA/2 | J:128519 | View | ||||
Kennedy's disease | Tg(Prnp-AR*112Q)#Deme/0 | involves: C57BL/6 * SJL | J:134789 | View | ||||
Lafora disease | Tg(CAG-EPM2A*C266S)1Bmin/0 | involves: 129 * C57BL/6 * SJL | J:262504, J:120356 | View | ||||
leukoencephalopathy with vanishing white matter | Tg(Plp1-Eif2ak3*)18Pop/Tg(Plp1-Eif2ak3*)18Pop | C57BL/6J-Tg(Plp1-Eif2ak3*)18Pop | J:216298 | 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 | ||||
Machado-Joseph disease | Tg(ATXN3*)67.2Cce/0 | involves: C57BL/6 * CBA | J:76495 | View | ||||
Machado-Joseph disease |
Tg(ATXN3*)67.2Cce/0 Tg(ATXN3*)84.2Cce/0 |
involves: C57BL/6 * CBA | J:76495 | View | ||||
Machado-Joseph disease | Tg(ATXN3*)84.2Cce/0 | involves: C57BL/6 * CBA | J:76495 | View | ||||
Machado-Joseph disease | Tg(ATXN3*)84.2Cce/Tg(ATXN3*)84.2Cce | involves: C57BL/6 * CBA | J:76495 | View | ||||
Machado-Joseph disease | Tg(CMV-ATXN3*94Q)94Pama/0 | B6.FVB-Tg(CMV-ATXN3*94Q)94Pama | J:163032 | View | ||||
Machado-Joseph disease | Tg(CMV-ATXN3*94Q)94Pama/Tg(CMV-ATXN3*94Q)94Pama | B6.FVB-Tg(CMV-ATXN3*94Q)94Pama | J:163032 | View | ||||
Machado-Joseph disease | Tg(CMV-ATXN3*135Q)CPama/0 | C57BL/6-Tg(CMV-ATXN3*135Q)CPama | J:222991 | View | ||||
Machado-Joseph disease | Tg(Htt-ATXN3*148Q)3746Thsc/0 | involves: C57BL/6N | J:156912 | View | ||||
Machado-Joseph disease | Tg(Pcp2-ATXN3*69Q)bHirai/0 | Not Specified | J:136101 | View | ||||
Machado-Joseph disease | Tg(Prnp-ATXN3*70Q)70.61Olri/0 | involves: C57BL/6N | J:122993 | View | ||||
Machado-Joseph disease | Tg(Prnp-ATXN3*79Q)#Hlw/0 | FVB/N-Tg(Prnp-ATXN3*79Q)#Hlw | J:138381 | View | ||||
Machado-Joseph disease | Tg(Prnp-ATXN3*148Q)148.19Olri/0 | involves: C57BL/6N | J:122993 | View | ||||
Machado-Joseph disease | Tg(Prnp-ATXN3*148Q)NLS.28Olri/0 | involves: C57BL/6N | J:122993 | 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 | ||||
McCune Albright syndrome |
Tg(Col1a1-tTA)139Niss/0 Tg(tetO-HTR4*D100A)2Niss/0 |
FVB/N-Tg(Col1a1-tTA)139Niss Tg(tetO-HTR4*D100A)2Niss | J:216100 | View | ||||
McCune Albright syndrome | Tg(EEF1A1-Gnas*R201C)184Pabi/0 | either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * FVB/N) | J:240241 | View | ||||
McCune Albright syndrome | Tg(PGK1-Gnas*R201C)60Pabi/0 | either: (involves: 129S6/SvEvTac * C57BL/6) or (involves: 129S6/SvEvTac * FVB/N) | J:240241 | View | ||||
myofibrillar myopathy 3 | Tg(ACTA1-MYOT*T57I)71Mah/? | involves: C57BL/6 * SJL | J:110377 | View | ||||
myofibrillar myopathy 6 | Tg(Myh6-BAG3*P209L)#Mswi/0 | involves: C57BL/6 * DBA/2 | J:234278 | View | ||||
nemaline myopathy 1 | Tg(ACTA1-TPM3*M9R)4Hrd/0 | FVB/NJ-Tg(ACTA1-TPM3*M9R)4Hrd | J:67596 | 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 | ||||
Netherton syndrome | Tg(IVL-KLK5)#Hov/0 | involves: C57BL/6 * CBA | J:210758 | View | ||||
neurodegeneration with brain iron accumulation 3 | Tg(PGK1-FTL*)#Sle/0 | B6J.FVB-Tg(PGK1-FTL*)#Sle | J:226967 | View | ||||
neurodegeneration with brain iron accumulation 3 | Tg(Prnp-FTL*)4Ruvi/Tg(Prnp-FTL*)4Ruvi | B6.C3Fe-Tg(Prnp-FTL*)4Ruvi | J:131053 | View | ||||
Noonan syndrome 1 |
H2az2Tg(Wnt1-cre)11Rth/H2az2+ Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0 |
involves: C57BL/6J * CBA/J * FVB/N | J:153094 | View | ||||
Noonan syndrome 1 |
Tg(CAG-cat,-Ptpn11*Q97R)1Rbns/0 Tg(Tek-cre)12Flv/0 |
involves: C3H * C57BL/6 * FVB/N | J:142212 | View | ||||
Noonan syndrome with multiple lentigines |
Tg(CAG-cat,-Ptpn11*Q510E)#Krnz/0 Tg(Tek-cre)1Ywa/0 |
involves: C57BL/6 * FVB/N * SJL | J:237450 | View | ||||
osteogenesis imperfecta type 1 | Tg(COL1A1)73Prc/0 | involves: FVB/N | J:146429 | View | ||||
Parkinson's disease 1 | Tg(PDGFB-SNCA)4Ema/0 | involves: C57BL/6 * DBA/2 | J:60638, J:166985 | View | ||||
Parkinson's disease 1 | Tg(PDGFB-SNCA*A53T)8Ema/0 | Not Specified | J:226922 | View | ||||
Parkinson's disease 1 | Tg(PDGFB-SNCA/EGFP)78Ema/0 | involves: C57BL/6 * DBA/2 | J:238692 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)25Mkle/0 | involves: C3H/HeJ * C57BL/6J | J:77344 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)83Vle/0 | involves: C3H * C57BL/6 | J:76657 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)83Vle/Tg(Prnp-SNCA*A53T)83Vle | involves: C3H * C57BL/6 | J:76657 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)AAub/? | involves: FVB/N | J:216589 | View | ||||
Parkinson's disease 1 | Tg(Prnp-SNCA*A53T)AAub/Tg(Prnp-SNCA*A53T)AAub | involves: FVB/N | J:181820, J:185489 | View | ||||
Parkinson's disease 1 | Tg(SNCA)ARyot/0 | C57BL/6J-Tg(SNCA)ARyot | J:185434 | View | ||||
Parkinson's disease 1 | Tg(SNCA*E46K)3Elan/? | involves: C57BL/6 * SJL | J:200740 | View | ||||
Parkinson's disease 1 | Tg(Snca-SNCA)#Galt/? | involves: C57BL/6 * DBA/2 | J:199939 | View | ||||
Parkinson's disease 1 | Tg(Th-SNCA*)1702Yosh/0 | involves: C3H * C57BL/6J | J:125149 | View | ||||
Parkinson's disease 1 | Tg(Thy1-SNCA)61Ema/0 | involves: C57BL/6 * DBA/2 | J:137490 | View | ||||
Parkinson's disease 1 | Tg(Thy1-SNCA*)#Ztzh/0 | involves: C57BL/6J | J:313970 | View | ||||
Parkinson's disease 1 | Tg(Thy1-SNCA*A30P)18Pjk/Tg(Thy1-SNCA*A30P)18Pjk | involves: C57BL/6 | J:80181 | View | ||||
Parkinson's disease 1 | Tg(THY1-SNCA*A53T)M53Sud/0 | B6.Cg-Tg(THY1-SNCA*A53T)M53Sud/J | J:212732 | View | ||||
Parkinson's disease 1 | Tg(Thy1-SNCA*E57K)16Ema/0 | involves: C57BL/6 * DBA/2 | J:236596 | View | ||||
Parkinson's disease 2 | Tg(Slc6a3-PARK2*Q311X)AXwy/0 | FVB/NJ-Tg(Slc6a3-PARK2*Q311X)AXwy | J:146833 | View | ||||
Parkinson's disease 8 | Tg(PDGFB-LRRK2*G2019S)32Hlw/? | FVB/N-Tg(PDGFB-LRRK2*G2019S)32Hlw | J:204793 | View | ||||
Parkinson's disease 8 | Tg(PDGFB-LRRK2*R1441C)31Hlw/0 | FVB/N-Tg(PDGFB-LRRK2*R1441C)31Hlw | J:229559 | View | ||||
PCWH syndrome | Tg(Venus/SOX10*)55Kein/0 | involves: C3H/He * C57BL/6 | J:227442 | View | ||||
PCWH syndrome | Tg(Venus/SOX10*)55Kein/Tg(Venus/SOX10*)55Kein | involves: C3H/He * C57BL/6 | J:227442 | View | ||||
Perry syndrome | Tg(Thy1-DCTN1*G71A)#Ytsu/0 | involves: C57BL/6J | J:258253 | View | ||||
polycystic kidney disease 2 | Tg(CAG-PKD2)#Hwl/? | involves: FVB/NJ | J:148377 | View | ||||
primary ciliary dyskinesia | Del(1)1Brk/Del(1)1Brk | involves: 129S6/SvEvTac * C57BL/6J * CBA/J | J:130396 | View | ||||
progeria |
Tg(KRT5-tTA)1216Glk/0 Tg(tetO-LMNA*G608G,-EGFP)VF1-07Maer/0 |
involves: FVB/N | J:145312 | View | ||||
progeria | Tg(LMNA*G608G)HClns/? | C57BL/6-Tg(LMNA*G608G)HClns/J | J:107176 | View | ||||
pseudoachondroplasia | Tg(Col2a1-rtTA,tetO-COMP*)2Jath/0 | C57BL/6-Tg(Col2a1-rtTA,tetO-COMP*)2Jath | J:152756, J:233238 | View | ||||
retinitis pigmentosa 4 |
Ntrk3tm1.1Tes/Ntrk3+ Tg(RHO*P347S)A1Tili/0 |
involves: 129S1/Sv * C57BL/6J * FVB/N | J:262975 | View | ||||
retinitis pigmentosa 4 | Tg(RHO*P347S)A1Tili/0 | involves: C57BL/6J * FVB/N | J:262975 | View | ||||
retinitis pigmentosa 4 | Tg(RHO-P23H)DTpd/? | involves: C57BL/6 * DBA/2 | J:76722 | View | ||||
schizophrenia 9 |
Tg(Camk2a-tTA)1Mmay/0 Tg(tetO-DISC1*)1001Plet/0 |
involves: C57BL/6 * CBA * SJL | J:146881 | View | ||||
schizophrenia 9 |
Tg(tetO-DISC1*)70Plet/0 Tg(Camk2a-tTA)1Mmay/0 |
involves: C57BL/6 * CBA * SJL | J:146881 | View | ||||
SOST-related sclerosing bone dysplasia | Rr20tm1.1Vlcg/Rr20tm1.1Vlcg | involves: 129S6/SvEvTac * C57BL/6NTac | J:188586 | View | ||||
SOST-related sclerosing bone dysplasia | Tg(RP11-209M4)AGglo/0 | FVB-Tg(RP11-209M4)4Gglo | J:99965 | View | ||||
SOST-related sclerosing bone dysplasia | Tg(RP11-209M4)AGglo/Tg(RP11-209M4)AGglo | FVB-Tg(RP11-209M4)4Gglo | J:99965 | View | ||||
spinocerebellar ataxia type 1 | Tg(Pcp2-ATXN1*82Q)5Horr/0 | involves: FVB/N | J:166951 | View | ||||
spinocerebellar ataxia type 1 |
Tg(Pcp2-tTA)3Horr/0 Tg(tetO-ATXN1*82Q)#Horr/Tg(tetO-ATXN1*82Q)#Horr |
involves: FVB/N | J:95453 | View | ||||
spinocerebellar ataxia type 2 | Tg(ATXN2*72Q)#Plt/0 | FVB/N-Tg(ATXN2*72Q)#Plt | J:224692 | View | ||||
spinocerebellar ataxia type 2 | Tg(Pcp2-ATXN2*127Q)#Plt/0 | involves: C57BL/6 * DBA/2 | J:191127 | View | ||||
spinocerebellar ataxia type 5 |
Tg(Pcp2-tTA)3Horr/0 Tg(tetO-SPTBN2*)#Lpwr/0 |
involves: FVB/N | J:215593 | View | ||||
spinocerebellar ataxia type 7 | Tg(GFAP-ATXN7*92Q)2521Als/0 | involves: C3H/HeJ * C57BL/6J | J:113150 | View | ||||
spinocerebellar ataxia type 7 | Tg(GFAP-ATXN7*92Q)2542Als/0 | involves: C3H/HeJ * C57BL/6J | J:113150 | View | ||||
spinocerebellar ataxia type 7 | Tg(Pcp2-SCA7)P7EJman/0 | involves: C57BL/6 * SJL | J:65411 | View | ||||
spinocerebellar ataxia type 7 | Tg(Prnp-ATXN7*92Q)1963Als/0 | B6J.Cg-Tg(Prnp-ATXN7*92Q)1963Als | J:222402 | View | ||||
spinocerebellar ataxia type 7 | Tg(Prnp-ATXN7*92Q)6076Als/0 | involves: C3H/HeJ * C57BL/6 | J:71971, J:77530, J:113150 | View | ||||
spinocerebellar ataxia type 7 | Tg(RHO-SCA7)R7EJman/0 | involves: C57BL/6 * SJL | J:65411 | View | ||||
spinocerebellar ataxia type 10 | Tg(Prnp-lacZ/ATXN10*)#Teas/0 | involves: FVB/N | J:222081 | View | ||||
spinocerebellar ataxia type 14 |
Tg(Pcp2-tTA)3Horr/0 Tg(tetO-PRKCG*S361G,-GFP)3Jpka/0 |
involves: FVB/N | J:218354 | View | ||||
spinocerebellar ataxia type 17 | Tg(Pcp2-TBP*)69Hmhl/0 | involves: FVB/N | J:174239 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)71-16Xjl/0 | FVB/N-Tg(Prnp-TBP*)71-16Xjl | J:130775 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)71-27Xjl/0 | FVB/N-Tg(Prnp-TBP*)71-27Xjl | J:130775 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)105Xjl/0 | FVB/N-Tg(Prnp-TBP*)105Xjl | J:130775 | View | ||||
Stargardt disease | Tg(RBP3-ELOVL4*)1Kzh/0 | C57BL/6-Tg(RBP3-ELOVL4*)1Kzh | J:97173 | View | ||||
Stargardt disease | Tg(RBP3-ELOVL4*)2Kzh/0 | C57BL/6-Tg(RBP3-ELOVL4*)2Kzh | J:97173 | View | ||||
Stargardt disease | Tg(RBP3-ELOVL4*)3Kzh/0 | C57BL/6-Tg(RBP3-ELOVL4*)3Kzh | J:97173 | View | ||||
syndromic X-linked intellectual disability Lubs type | Tg(MECP2)1Hzo/0 | either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1 | J:181213 | View | ||||
syndromic X-linked intellectual disability Lubs type | Tg(MECP2)1Hzo/0 | FVB-Tg(MECP2)1Hzo/J | J:253720 | View | ||||
syndromic X-linked intellectual disability Lubs type | Tg(MECP2)3Hzo/0 | either: (FVB/N x 129S6/SvEvTac)F1 or (FVB/N x C57BL/6J)F1 | J:181213 | View | ||||
torsion dystonia 1 | Tg(CMV-TOR1A*)1Nush/0 | involves: C3H * C57BL/6 | J:98716 | View | ||||
torsion dystonia 1 | Tg(CMV-TOR1A*)2Nush/0 | involves: C3H * C57BL/6 | J:98716 | View | ||||
torsion dystonia 1 | Tg(Eno2-TOR1A*)13Shas/0 | involves: C3H * C57BL/6J | J:95447 | View | ||||
transthyretin amyloidosis |
Hsf1tm1Ijb/Hsf1tm1Ijb Tg(TTR-V30M)15Imeg/0 |
involves: 129S6/SvEvTac * BALB/c * C57BL/6 | J:156658 | View | ||||
transthyretin amyloidosis | Tg(TTR-V30M)15Imeg/0 | involves: C57BL/6 | J:260683 | View | ||||
transthyretin amyloidosis | Tg(TTR-V30M)15Imeg/0 | Not Specified | J:80880 | View | ||||
tuberous sclerosis |
Emx1tm1(cre)Ito/Emx1+ Tg(CAG-Mtor*)#Atai/0 |
involves: 129P2/OlaHsd * C57BL/6 * DBA/2 * ICR | J:211789 | View | ||||
Werner syndrome | Tg(CAG-WRN*K577M)5025Wcl/0 | involves: C3H * C57BL/6J | J:95127 | View | ||||
X-linked dominant hypophosphatemic rickets | Tg(APOE-FGF23*R176Q)#Ack/0 | involves: C57BL/6J * CBA | J:93981 | View | ||||
X-linked dominant hypophosphatemic rickets | Tg(Col1a1-FGF2*,-Sapphire)203Mmh/Tg(Col1a1-FGF2*,-Sapphire)203Mmh | involves: FVB/N | J:240777 | View | ||||
Additional Complex Models | abdominal obesity-metabolic syndrome |
Ay/a Apoetm1Unc/Apoetm1Unc |
involves: 129P2/OlaHsd * C57BL/6J * KK/TaJcl | J:177084 | View | |||
abdominal obesity-metabolic syndrome |
Apoetm1Unc/Apoetm1Unc Cyp19a1tm1Esi/Cyp19a1tm1Esi |
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6 | J:184647 | View | ||||
age related macular degeneration |
Abca4tm1Kpal/Abca4tm1Kpal Rdh8tm1Kpal/Rdh8tm1Kpal |
involves: 129 | J:213619 | View | ||||
age related macular degeneration 1 |
Cptm1Hrs/Cptm1Hrs Hephsla/Y |
involves: 129X1/SvJ * C57BL/6 | J:136925 | View | ||||
Alzheimer's disease 3 |
Tg(APP695)3Dbo/0 Tg(PSEN1)5Dbo/0 |
involves: C3H/HeJ * C57BL/6J | J:43788 | View | ||||
amyotrophic lateral sclerosis type 1 |
Tg(SOD1)2Gur/0 Tg(SOD1*A4V)A1073Gur/0 |
involves: C57BL/6 * SJL | J:109458 | View | ||||
autosomal recessive pseudohypoaldosteronism type 1 |
Scnn1atm1Rss/Scnn1atm1Rss Tg(CMV-Scnn1a)1352Rss/0 |
involves: 129P2/OlaHsd * NMRI | J:43583 | View | ||||
Birt-Hogg-Dube syndrome |
Fnip1tm1.2Baba/Fnip1+ Fnip2tm1.2Lss/Fnip2tm1.2Lss |
involves: C57BL/6 | J:220672 | View | ||||
brachydactyly type A1 | ShhDsh/Shh+ | B10Rl.Cg-ShhDsh | J:97323 | View | ||||
CADASIL 1 |
Gt(ROSA)26Sortm3(NOTCH3*R1031C)Sat/Gt(ROSA)26Sor+ Tg(Tagln-cre)1Her/0 |
involves: 129S2/SvPas * 129S6/SvEvTac * C57BL/6 * SJL | J:171887 | 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 | ||||
CINCA Syndrome |
Prkacatm1Gsm/Prkaca+ Prkar1atm1.1Lsk/Prkar1a+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:166728 | View | ||||
cone-rod dystrophy |
Aipl1tm1Visu/Aipl1tm1Visu Tg(Crx-AIPL1*P351)#Visu/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * FVB/N | J:218096 | View | ||||
cone-rod dystrophy | Gt(ROSA)26Sortm1.1(CAG-ATP1A3*D591V,-EGFP)Bcgen/Gt(ROSA)26Sor+ | involves: C57BL/6 | J:319361 | View | ||||
dilated cardiomyopathy 1A |
H2-Ab1b-tm1Gru/H2-Ab1b-tm1Gru Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell/Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell |
NOD.Cg-H2-Ab1b-tm1Gru Tg(CD2-CD4,HLA-DQA1,HLA-DQB1)1Ell | J:86540 | View | ||||
Ehlers-Danlos syndrome spondylodysplastic type 2 |
Bgntm1Mfy/Y Dcntm1Ioz/Dcntm1Ioz |
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ | J:91512 | 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 4 | Gt(ROSA)26Sortm1.1(CAG-SPAST*C448Y)Baas/Gt(ROSA)26Sortm1.1(CAG-SPAST*C448Y)Baas | involves: C57BL/6N | J:273408 | View | ||||
Hermansky-Pudlak syndrome |
Rab32tm1b(KOMP)Wtsi/Rab32tm1b(KOMP)Wtsi Rab38tm1.1Ics/Rab38tm1.1Ics |
involves: C57BL/6N * C57BL/6NTac | J:293385 | View | ||||
hyper IgE recurrent infection syndrome 1 |
Igh-Jtm1Mcdl/Igh-Jtm1Mcdl Igk-Jtm1Mcdl/Igk-Jtm1Mcdl Rag1tm1Mom/Rag1tm1Mom Tg(DO11.10)10Dlo/? |
involves: 129S/Sv * BALB/c * C3H * C57BL/6 | J:100072 | View | ||||
Machado-Joseph disease |
Prnptm1Cwe/Prnptm1Cwe Tg(Prnp-tTA)F959Sbp/0 Tg(tetO-ATXN3)2904Olri/Tg(tetO-ATXN3)2904Olri |
involves: 129S7/SvEvBrd * C57BL/6 * FVB | J:154079 | View | ||||
Machado-Joseph disease |
Prnptm1Cwe/Prnptm1Cwe Tg(Prnp-tTA)F959Sbp/Tg(Prnp-tTA)F959Sbp Tg(tetO-ATXN3)2904Olri/0 |
involves: 129S7/SvEvBrd * C57BL/6 * FVB | J:154079 | View | ||||
Machado-Joseph disease |
Prnptm1Cwe/Prnptm1Cwe Tg(Prnp-tTA)F959Sbp/Tg(Prnp-tTA)F959Sbp Tg(tetO-ATXN3)2904Olri/Tg(tetO-ATXN3)2904Olri |
involves: 129S7/SvEvBrd * C57BL/6 * FVB | J:154079 | View | ||||
maturity-onset diabetes of the young |
Foxo1tm1Rdp/Foxo1tm1Rdp Foxo3tm1Rdp/Foxo3tm1Rdp Foxo4tm1Rdp/Foxo4tm1Rdp Tg(Ins2-cre)23Herr/0 |
involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * CBA/J | J:215526 | View | ||||
neurofibromatosis 1 |
Krastm4Tyj/Kras+ Ptentm1Hwu/Pten+ Tg(Gfap-cre)77.6Mvs/0 |
involves: 129S4/SvJae * BALB/c * C57BL/6NHsd | J:154673 | View | ||||
Parkinson's disease 1 | 2310039L15RikTg(Prnp-SNCA*A53T)23Mkle/0 | involves: C3H/HeJ * C57BL/6J | J:77344 | View | ||||
Parkinson's disease 1 |
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo 7630403G23RikTg(Th-cre)1Tmd/7630403G23Rik+ |
involves: 129 * C57BL/6 | J:150777 | View | ||||
Parkinson's disease 1 |
Gt(ROSA)26Sortm2(SNCA*119)Djmo/Gt(ROSA)26Sortm2(SNCA*119)Djmo 7630403G23RikTg(Th-cre)1Tmd/7630403G23Rik+ |
involves: 129 * C57BL/6 * SJL | J:150777 | View | ||||
Parkinson's disease 8 | Khdrbs2Tg(LRRK2*R1441G)135Cjli/Khdrbs2+ | FVB-Khdrbs2Tg(LRRK2*R1441G)135Cjli | J:149135 | View | ||||
Parkinson's disease 8 | Khdrbs2Tg(LRRK2*R1441G)135Cjli/Khdrbs2+ | FVB/N-Khdrbs2Tg(LRRK2*R1441G)135Cjli/J | J:204940 | View | ||||
primary ciliary dyskinesia | Ak7Tg(tetO-Hmox1)67Sami/Ak7Tg(tetO-Hmox1)67Sami | FVB/N-Ak7Tg(tetO-Hmox1)67Sami | J:186062 | View | ||||
spondyloepiphyseal dysplasia congenita |
Gt(ROSA)26Sortm5(ACTB-tTA)Luo/Gt(ROSA)26Sor+ Tg(Col2a1-cre)1Bhr/0 Tg(tetO/CMV-Col2a1*R992C,-GFP)#Afe/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/6J * SJL | J:216945 | View |
No similarity to the expected human disease phenotype was found.
|
||||||||
Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
NOT Models | adrenoleukodystrophy | Acsbg1tm1Mld/Acsbg1tm1Mld | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:150391 | View | |||
Alzheimer's disease 3 | Psen1tm1Psgh/Psen1tm1Psgh | Not Specified | J:66016 | View | ||||
amelogenesis imperfecta type 1E | Tg(Amelx)42Msnd/Tg(Amelx)42Msnd | involves: C57BL/6J * CBA/J * DBA/2J | J:100004 | View | ||||
autosomal dominant nocturnal frontal lobe epilepsy 1 | Chrna4tm1Dra/Chrna4tm1Dra | involves: 129S4/SvJae * C57BL/6 | J:64208, J:97020 | View | ||||
autosomal dominant nonsyndromic deafness 2A | Gjb3tm1Kwi/Gjb3tm1Kwi | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:68014 | View | ||||
autosomal dominant nonsyndromic deafness 15 | Pou4f3tm1Rsd/Pou4f3+ | involves: 129S4/SvJae * C57BL/6 | J:57149 | View | ||||
autosomal dominant nonsyndromic deafness 65 |
Cdh23Ahl+/Cdh23Ahl+ Tbc1d24em4Tbf/Tbc1d24em4Tbf |
B6.Cg-Cdh23Ahl+ Tbc1d24em4Tbf | J:299025 | View | ||||
autosomal dominant nonsyndromic deafness 65 | Tbc1d24em4Tbf/Tbc1d24em4Tbf | C57BL/6J-Tbc1d24em4Tbf | J:299025 | View | ||||
autosomal recessive limb-girdle muscular dystrophy type 2E | Sgcbem1Isrd/Sgcbem1Isrd | involves: 129 * C57BL/6N | J:257027 | View | ||||
autosomal recessive nonsyndromic deafness 86 | Tbc1d24em3Tbf/Tbc1d24em3Tbf | C57BL/6J-Tbc1d24em3Tbf | J:299025 | View | ||||
autosomal recessive polycystic kidney disease | Pkhd1tm1Rbu/Pkhd1tm1Rbu | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:112509 | View | ||||
beta thalassemia | Del(7Or2h1-Rr320)1Mkg/+ | involves: 129 | J:139198 | View | ||||
CADASIL 1 | Notch3tm1Grid/Notch3tm1Grid | involves: 129S1/Sv * C57BL/6 | J:227333 | View | ||||
CADASIL 1 | Notch3tm1Ul/Notch3+ | Not Specified | J:95927 | View | ||||
CADASIL 1 | Notch3tm1Ul/Notch3tm1Ul | Not Specified | J:95927 | View | ||||
Charcot-Marie-Tooth disease type 2B1 | Lmnatm1.1Vde/Lmnatm1.1Vde | B6.129(Cg)-Lmnatm1.1Vde | J:322912 | View | ||||
cherubism |
Sh3bp2tm1Bjro/Sh3bp2tm1Bjro Tnftm1Gkl/Tnftm1Gkl |
involves: 129S/SvEv * 129S4/SvJae * BALB/cJ * C57BL/6J | J:117880 | View | ||||
cleft lip-palate-ectodermal dysplasia syndrome |
Nectin1tm1Ytk/Nectin1+ Nectin3tm1Ytk/Nectin3tm1Ytk |
involves: 129X1/SvJ * C57BL/6 | J:165548 | View | ||||
cleft lip-palate-ectodermal dysplasia syndrome | Nectin1tm1Ytk/Nectin1tm1Ytk | involves: 129X1/SvJ * C57BL/6 | J:165548 | View | ||||
cleft lip-palate-ectodermal dysplasia syndrome |
Nectin1tm1Ytk/Nectin1tm1Ytk Nectin3tm1Ytk/Nectin3+ |
involves: 129X1/SvJ * C57BL/6 | J:165548 | View | ||||
complex cortical dysplasia with other brain malformations 7 | Tuba8tm1.2Ctpd/Tuba8tm1.2Ctpd | involves: 129P2/OlaHsd * C57BL/6J | J:248203 | View | ||||
developmental and epileptic encephalopathy 14 | Kcnt1em1Pqt/Kcnt1+ | C57BL/6J-Kcnt1em1Pqt | J:333512 | View | ||||
dilated cardiomyopathy 1D | Tnnt2tm1Mmto/Tnnt2+ | involves: 129S/SvEv | J:141967 | View | ||||
Donohue syndrome | Insrtm1Dac/Insrtm1Dac | involves: 129S4/SvJae * C57BL/6 | J:33408 | View | ||||
Donohue syndrome | Insrtm1Jja/Insrtm1Jja | involves: 129S2/SvPas * C57BL/6 * DBA/2 | J:32538 | View | ||||
dysplastic nevus syndrome | Cdkn2atm1Rdp/Cdkn2atm1Rdp | involves: 129/Sv * C57BL/6 * SJL | J:53805 | View | ||||
familial medullary thyroid carcinoma | Rettm2.1Cos/Ret+ | involves: 129S1/Sv * C57BL/6J * FVB/N | J:60659 | View | ||||
familial medullary thyroid carcinoma | Rettm2.1Cos/Rettm2.1Cos | involves: 129S1/Sv * C57BL/6J * FVB/N | J:60659 | View | ||||
Fanconi anemia complementation group P | Slx4tm1.2Jrou/Slx4tm1.2Jrou | B6.129P2-Slx4tm1.2Jrou | J:204996 | View | ||||
focal segmental glomerulosclerosis 1 | Tg(CMV-Plaur*)19Lbh/0 | FVB/N-Tg(CMV-Plaur*)19Lbh | J:217443 | View | ||||
Fraser syndrome | Frem3em1Osb/Frem3em1Osb | involves: C57BL/6NJcl * DBA/2NJcl | J:291067 | View | ||||
Hailey-Hailey disease | Atp2c1tm1Ges/Atp2c1+ | involves: 129X1/SvJ * Black Swiss | J:124662 | View | ||||
hereditary spastic paraplegia 2 |
Plp1tm1c(EUCOMM)Wtsi/Y Neurod6tm1(cre)Kan/Neurod6+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N | J:245100 | View | ||||
hereditary spastic paraplegia 8 | Washc5tm1.2Cbee/Washc5+ | involves: C57BL/6 | J:266630 | View | ||||
holoprosencephaly 4 | Tgif1tm1.1Caw/Tgif1tm1.1Caw | involves: C57BL/6 * FVB/N | J:97642 | View | ||||
hypomyelinating leukodystrophy 7 | Polr3aGt(LG04)Osb/Polr3atm1Bebr | involves: C57BL/6 * C57BL/6J * DBA/2 | J:250577 | View | ||||
hypomyelinating leukodystrophy 7 | Polr3atm1.1Bebr/Polr3atm1.1Bebr | involves: C57BL/6J | J:250577 | View | ||||
immunodeficiency 24 | Ctps1em1Slat/Ctps1em1Slat | C57BL/6J-Ctps1em1Slat | J:348981 | View | ||||
inflammatory bowel disease 12 | Gnai2tm1Lbi/Gnai2tm1Lbi | 129-Gnai2tm1Lbi | J:91100 | View | ||||
Leber congenital amaurosis 9 | Nmnat1tm1Ruch/Nmnat1tm1Ruch | involves: 129S7/SvEvBrd | J:267630 | View | ||||
mandibulofacial dysostosis, Guion-Almeida type | Eftud2em1Lajm/Eftud2+ | involves: C57BL/6 | J:278323 | View | ||||
mandibulofacial dysostosis, Guion-Almeida type | Eftud2em2Lajm/Eftud2+ | involves: CD-1 * FVB/N | J:278323 | View | ||||
mitochondrial DNA depletion syndrome 1 | Tymptm1Akiy/Tymptm1Akiy | involves: 129X1/SvJ | J:78036 | View | ||||
mitochondrial DNA depletion syndrome 1 |
Tymptm1Akiy/Tymptm1Akiy Upp1tm1Akiy/Upp1tm1Akiy |
involves: 129X1/SvJ | J:78036 | View | ||||
Mowat-Wilson syndrome | Zeb2tm1.2Yhi/Zeb2+ | involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:82084 | View | ||||
multiple endocrine neoplasia type 2B | Rettm1Cos/Rettm2.1Cos | involves: 129S/SvEv * 129S1/Sv * C57BL/6J * FVB/N * MF1 | J:60659 | View | ||||
myofibrillar myopathy 3 | Myottm1.1Moza/Myottm1.1Moza | involves: 129S1/Sv * 129X1/SvJ * ICR | J:117709 | View | ||||
nephronophthisis 1 | Nphp1tm1.1Hung/Nphp1tm1.1Hung | B6.Cg-Nphp1tm1.1Hung | J:140205 | View | ||||
neurofibromatosis 1 | Nf1tm1Tyj/Nf1+ | involves: 129S2/SvPas * C57BL/6 | J:18542 | View | ||||
Noonan syndrome 1 | Ptpn11tm1Paw/Ptpn11tm1Paw | involves: 129S1/Sv * 129X1/SvJ * CD-1 | J:43740 | View | ||||
Noonan syndrome 1 | Ptpn11tm1Rbn/Ptpn11+ | involves: 129 * Black Swiss | J:35137 | View | ||||
Noonan syndrome 1 | Ptpn11tm1Rbn/Ptpn11tm1Rbn | involves: 129 * Black Swiss | J:35137 | View | ||||
oculocerebrorenal syndrome | Ocrltm1Nbm/Ocrltm1Nbm | either: (involves: 129S/SvEv * C57BL/6) or (involves: 129S/SvEv * NIH Black Swiss) | J:47884 | View | ||||
osteogenesis imperfecta type 5 | Ifitm5em1Pmof/Ifitm5+ | involves: CD-1 | J:255349 | View | ||||
pantothenate kinase-associated neurodegeneration | Pank2tm1Jgt/Pank2tm1Jgt | involves: 129X1/SvJ * C57BL/6J | J:94753 | View | ||||
paraganglioma |
Sdhctm1c(EUCOMM)Wtsi/Sdhctm1c(EUCOMM)Wtsi Gt(ROSA)26Sortm1.1(rtTA,tetO-cre)Bkmn/Gt(ROSA)26Sor+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6N | J:284745 | View | ||||
paraganglioma | Sdhdtm1Jlob/Sdhd+ | involves: 129X1/SvJ | J:95252 | View | ||||
paraganglioma | Sdhdtm1Jlob/Sdhdtm1Jlob | involves: 129X1/SvJ | J:95252 | View | ||||
paraganglioma | Sdhdtm1Jpb/Sdhd+ | either: 129P2/OlaHsd-Sdhdtm1Jpb or (involves: 129P2/OlaHsd * C57BL/6J) | J:155380 | View | ||||
Pendred Syndrome | Slc26a4tm2.1Dontu/Slc26a4tm2.1Dontu | B6.129-Slc26a4tm2.1Dontu | J:203206 | View | ||||
Pierson syndrome | Lamb2em1Jhm/Lamb2em1Jhm | involves: C57BL/6J * CBA/J | J:280129 | View | ||||
Pierson syndrome |
Lamb2tm1Jrs/Lamb2tm1Jrs Tg(Ckm-Lamb2)1Jhm/0 Tg(Nphs1-Lamb2*S83R)#Jhm/0 |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CBA | J:280129 | View | ||||
progeria | Lmnatm5Lgf/Lmnatm5Lgf | involves: 129P2/OlaHsd * C57BL/6 | J:160705 | View | ||||
progeria | Lmnatm8Lgf/Lmnatm8Lgf | involves: 129P2/OlaHsd | J:167229 | View | ||||
pseudoachondroplasia | Comptm1Aol/Comptm1Aol | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:76781 | View | ||||
retinitis pigmentosa 11 | Prpf31tm1Bha/Prpf31+ | involves: 129S2/SvPas * C57BL/6J | J:158261 | View | ||||
retinitis pigmentosa 18 | Prpf3Gt(RRO284)Byg/Prpf3+ | involves: 129P2/OlaHsd * C57BL/6 | J:141780 | View | ||||
Sotos syndrome | Nsd1tm1.1Pcn/Nsd1tm1.1Pcn | involves: 129/Sv * C57BL/6 | J:83923 | View | ||||
spinocerebellar ataxia type 5 | Sptbn2tm1Mjac/Sptbn2+ | involves: 129P2/OlaHsd | J:163169 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)13Xjl/0 | FVB/N-Tg(Prnp-TBP*)13Xjl | J:130775 | View | ||||
Stargardt disease | Elovl4tm1Sie/Elovl4+ | involves: 129P2/OlaHsd * C57BL/6 | J:112264 | View | ||||
Stargardt disease | Elovl4tm1Sie/Elovl4tm1Sie | involves: 129P2/OlaHsd * C57BL/6 | J:112264 | View | ||||
Stromme syndrome | Cenpfem3Bko/Cenpfem3Bko | involves: C57BL/6 * C57BL/6NTac * DBA/2 | J:273098 | View | ||||
tibial muscular dystrophy |
Capn3tm1Jsb/Capn3+ Ttntm1.1Isrd/Ttn+ |
involves: 129/Sv * 129S2/SvPas * C57BL/6 | J:165576 | View | ||||
triple-A syndrome | Aaastm1Ahue/Aaastm1Ahue | involves: 129P2/OlaHsd * C57BL/6 | J:106908 | View | ||||
type 1 diabetes mellitus 2 | Hk2tm1Laak/Hk2+ | involves: 129P2/OlaHsd * BALB/c * DBA/2 | J:56644 | View | ||||
Usher syndrome type 1J | Cib2tm1.1Aela/Cib2tm1.1Aela | involves: BALB/c * C57BL/6 * C57BL/6N | J:262464 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-2H/Pax3+ | involves: C57BL/6 | J:14096 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-2H/Pax3Sp-2H | involves: 101 * C3H/He * CBA/Ca | J:46341 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-2H/Pax3Sp-2H | involves: C57BL/6 | J:14096 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-d/Pax3+ | C57BL/6J-Pax3Sp-d | J:238 | View | ||||
Waardenburg syndrome type 3 | Pax3Sp-d/Pax3Sp-d | C57BL/6J-Pax3Sp-d | J:238 | View | ||||
Williams-Beuren syndrome | Fzd9tm1Uta/Fzd9tm1Uta | involves: 129S6/SvEvTac * 129X1/SvJ | J:98133 | View | ||||
X-linked ichthyosis | Foxp3sf/Y | either: 129Rl.Cg-Foxp3sf or (involves: 101/Rl * C3Hf/Rl * STOCK MR) | J:11262 | View | ||||
X-linked ichthyosis | Foxp3sf/Y | involves: STOCK MR | J:14076 | View | ||||
X-linked severe combined immunodeficiency | Il2rgtm1Cgn/Il2rgtm1Cgn | involves: 129 * CB20 | J:22521 | View | ||||
X-linked severe combined immunodeficiency | Il2rgtm1Cgn/Y | involves: 129 * CB20 | J:22521 | View | ||||
X-linked severe combined immunodeficiency | Il2rgtm1Sug/Y | either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129S6/SvEvTac * C57BL/6) | J:31167 | View |