![]() ![]() |
||||||||
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 | ||||
achromatopsia 2 | \Cnga3cpfl5/\Cnga3cpfl5 | B6.RHJ-Cnga3cpfl5/BocJ | J:187090, J:358897 | 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 | ||||
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 | ||||
alacrima, achalasia, and impaired intellectual development syndrome | \Gmppatm1d(EUCOMM)Wtsi/\Gmppatm1d(EUCOMM)Wtsi | involves: C57BL/6N | J:305791 | 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 | ||||
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 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 | ||||
antithrombin III deficiency | \Serpinc1tm1Dwr/\Serpinc1tm1Dwr | involves: 129S1/Sv * 129X1/SvJ | J:115658 | 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 | ||||
atrichia with papular lesions | \Hrrh-8J/\Hrrh-8J | B10.D2/nSnJ-Hrrh-8J | J:50909 | View | ||||
atrichia with papular lesions | \Hrrhsl/\Hrrhsl | involves: BALB/c | J:98859 | View | ||||
autoimmune lymphoproliferative syndrome type 2B |
\Casp8tm1Raz/\Casp8tm1Raz \Tg(Lck-cre)548Jxm/0 |
involves: 129P2/OlaHsd * C57BL/6 * CBA | J:107455 | View | ||||
autosomal 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 |
\Tmtc4em1Dkc/\Tmtc4em1Dkc \Myo15atm1.1(cre)Ugds/\Myo15a+ |
involves: 129S1/SvImJ * C57BL/6J | J:351171 | View | ||||
autosomal recessive nonsyndromic deafness |
\Tmtc4em1Dkc/\Tmtc4em1Dkc \Tg(Atoh1-cre)1Bfri/0 |
involves: C57BL/6 * C57BL/6J * CBA | J:351171 | 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 | \Pjvkem1Chchw/\Pjvkem1Chchw | C57BL/6J-Pjvkem1Chchw | J:332624 | 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 | ||||
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 | ||||
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 | ||||
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 | ||||
Bowen-Conradi syndrome | \Emg1tm1.1Btr/\Emg1tm1.1Btr | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * CD-1 | J:230556 | View | ||||
brachyolmia-amelogenesis imperfecta syndrome | \Ltbp3tm1Bdvc/\Ltbp3tm1Bdvc | involves: 129S6/SvEvTac | J:220985 | View | ||||
branched-chain keto acid dehydrogenase kinase deficiency | \BckdkGt(VICT48)710Lex/\BckdkGt(VICT48)710Lex | B6.129S5/SvEvBrd-BckdkGt(VICT48)710Lex | J:187971 | View | ||||
brittle cornea syndrome 1 | \Zfp469em1Chms/\Zfp469em1Chms | C57BL/6J-Zfp469em1Chms | J:311083 | 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 | ||||
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 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 | ||||
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 | ||||
Charcot-Marie-Tooth disease axonal type 2K | \Gdap1tm1.2Geno/\Gdap1tm1.2Geno | involves: 129 * C57BL/6 | J:224701 | 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 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 recessive intermediate D | \Cox6a1tm1(KOMP)Wtsi/\Cox6a1tm1(KOMP)Wtsi | involves: C57BL/6JJcl * C57BL/6N | J:230212 | View | ||||
Charcot-Marie-Tooth disease type 2B1 | \Lmnatm1Stw/\Lmnatm1Stw | involves: 129S1/Sv | J:75378 | 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 | ||||
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 | ||||
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 | ||||
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 | ||||
Cohen syndrome | \Vps13btm1.2Ics/\Vps13btm1.2Ics | involves: C57BL/6N | J:296007 | 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 | ||||
congenital afibrinogenemia | \Fggtm1Fjc/\Fggtm1Fjc | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:75302 | 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 hereditary endothelial dystrophy of cornea | \Slc4a11tm1.1Jrcy/\Slc4a11tm1.1Jrcy | involves: C57BL/6 | J:214272 | 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 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 nonspherocytic hemolytic anemia 2 | \Pklrchar4/\Pklrchar4 | involves: A/J * C57BL/6 | J:86735 | View | ||||
congenital nonspherocytic hemolytic anemia 2 | \Pklrslc/\Pklrslc | CBA/NSlc-Pklrslc | J:29199 | View | ||||
congenital secretory chloride diarrhea 1 | \Slc26a3tm1Sole/\Slc26a3tm1Sole | involves: 129S6/SvEvTac * C57BL/6 | J:117587 | View | ||||
congenital stationary night blindness 1B | \Grm6nob7/\Grm6nob7 | C57BL/6J-Grm6nob7 | J:229885 | View | ||||
congenital stationary night blindness 1B | \Grm6nob8/\Grm6nob8 | CBA/CaJ | J:240996 | View | ||||
congenital stationary night blindness 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 | ||||
cortical dysplasia-focal epilepsy syndrome | \Cntnap2tm1Pele/\Cntnap2tm1Pele | B6.129-Cntnap2tm1Pele | J:177110 | 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 | ||||
developmental and epileptic encephalopathy 16 | \Tbc1d24em2Tbf/\Tbc1d24em2Tbf | C57BL/6J-Tbc1d24em2Tbf | J:273646 | View | ||||
developmental and epileptic encephalopathy 37 | \Frrs1ltm1b(EUCOMM)Hmgu/\Frrs1ltm1b(EUCOMM)Hmgu | C57BL/6N-Frrs1ltm1b(EUCOMM)Hmgu/H | J:272893 | View | ||||
developmental and epileptic encephalopathy 39 | \Slc25a12Gt(OST123999)Lex/\Slc25a12Gt(OST123999)Lex | involves: 129S5/SvEvBrd * C57BL/6 | J:243212 | 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 | ||||
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 | ||||
EAST syndrome | \Kcnj10tm1Lst/\Kcnj10tm1Lst | involves: 129S1/Sv | J:226598 | View | ||||
EAST syndrome | \Kcnj10tm1Lst/\Kcnj10tm1Lst | involves: 129S1/Sv * C57BL/6J | J:77663 | 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 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 | ||||
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 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 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 | ||||
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 | ||||
fibular hypoplasia and complex brachydactyly | \Gdf5Bp-5J/\Gdf5+ | C57BL/6J-Gdf5Bp-5J/GrsrJ | J:200816 | View | ||||
foveal hypoplasia 2 | \Slc38a8em1Lmon/\Slc38a8em1Lmon | B6.Cg-Slc38a8em1Lmon | J:343795 | 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 | ||||
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 | ||||
glycine encephalopathy | \GldcGt(EUCG0001d02)Hmgu/\GldcGt(EUCG0001d02)Hmgu | B6.129P2-GldcGt(EUCG0001d02)Hmgu | J:221782 | 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-cre/ERT2)64.9Ics/0 |
involves: 129S2/SvPas * FVB/N | 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 Ib | \Slc37a4tm1Jyc/\Slc37a4tm1Jyc | involves: 129S4/SvJae * C57BL/6 | J:86005 | 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 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 | ||||
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 | ||||
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 | ||||
hereditary sensory and autonomic neuropathy type 6 | \Dstdt-23Rbrc/\Dstdt-23Rbrc | involves: C3H/HeN * C57BL/6 | J:251779 | 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 15 | \Zfyve26tm1.1Cahb/\Zfyve26tm1.1Cahb | involves: 129S1/Sv * 129X1/SvJ * BALB/cJ * C57BL/6 | J:223127 | View | ||||
hereditary spastic paraplegia 35 | \Fa2htm1.1Hama/\Fa2htm1.1Hama | involves: 129 * C57BL/6 | J:171655 | View | ||||
hereditary spastic paraplegia 48 | \Ap5z1tm1(KOMP)Wtsi/\Ap5z1tm1(KOMP)Wtsi | involves: 129 * C57BL/6N | J:283611 | View | ||||
hereditary spastic paraplegia 54 | \Ddhd2tm1Crv/\Ddhd2tm1Crv | involves: C57BL/6 | J:216446 | View | ||||
hereditary spherocytosis type 1 | \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 | ||||
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 | ||||
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 7 |
\Polr3atm1Iwil/\Polr3atm1Iwil \Olig2tm1.1(cre)Wdr/\Olig2+ |
involves: 129S1/Sv * 129X1/SvJ * C57BL/6J | J:311745 | View | ||||
hypomyelinating leukodystrophy 7 |
\Polr3atm1Iwil/\Polr3atm1Iwil \Tg(CAG-cre/Esr1*)5Amc/0 |
Not Specified | J:364909 | 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 | ||||
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 | ||||
isolated microphthalmia 6 | \Prss56em2(IMPC)J/\Prss56em2(IMPC)J | C57BL/6NJ-Prss56em2(IMPC)J/Mmjax | J:364267 | View | ||||
isolated microphthalmia 6 | \Prss56glcr4/\Prss56glcr4 | B6(Cg)-Prss56glcr4/Sj | J:188765 | View | ||||
isolated microphthalmia 6 | \Prss56glcr4/\Prss56glcr4 | C3A.Cg-Prss56glcr4 Pde6b+ | J:188765 | View | ||||
isolated microphthalmia 6 | \Prss56glcr4/\Prss56glcr4 | involves: C3H/HeA * C57BL/6J * C57BL/LiA | J:188765 | View | ||||
Johanson-Blizzard syndrome | \Ubr1tm1Avar/\Ubr1tm1Avar | involves: 129S1/Sv * C57BL/6 | J:105229 | View | ||||
junctional epidermolysis bullosa with pyloric atresia | \Itgb4tm1Fgg/\Itgb4tm1Fgg | involves: 129S1/Sv * C57BL/6 | J:48924 | View | ||||
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 | ||||
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 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 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 12 | \Rd3rd3/\Rd3rd3 | RBF/DnJ-Rd3rd3 | J:202634 | View | ||||
Leber congenital amaurosis 14 | \Lrattm1Kpal/\Lrattm1Kpal | involves: 129S6/SvEvTac | J:136882 | View | ||||
leukocyte adhesion deficiency 1 | \Itgb2tm1Bay/\Itgb2tm1Bay | involves: 129S7/SvEvBrd | J:13599 | View | ||||
leukocyte adhesion deficiency 1 | \Itgb2tm1Bay/\Itgb2tm1Bay | involves: 129S7/SvEvBrd * C57BL/6J | J:13599 | View | ||||
leukocyte adhesion deficiency 1 | \Itgb2tm2Bay/\Itgb2tm2Bay | involves: 129S7/SvEvBrd * C57BL/6J | J:48542 | View | ||||
leukocyte adhesion deficiency 3 | \Fermt3tm1Ref/\Fermt3tm1Ref | involves: 129S1/Sv * 129X1/SvJ | J:146783 | View | ||||
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 | ||||
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 | ||||
megaconial type congenital muscular dystrophy | \Chkbrmd/\Chkbrmd | involves: BALB/cByJ * C57BL/6J | J:108320 | View | ||||
megalencephalic leukoencephalopathy with subcortical cysts 1 | \Mlc1tm1.1Vdk/\Mlc1tm1.1Vdk | involves: C57BL/6 | J:250520, J:244698 | View | ||||
microcephalic osteodysplastic primordial dwarfism type II | \PcntGt(RRU388)Byg/\PcntGt(RRU388)Byg | B6.129P2-PcntGt(RRU388)Byg | J:226309 | View | ||||
microphthalmia with limb anomalies | \Smoc1tm1a(EUCOMM)Wtsi/\Smoc1tm1a(EUCOMM)Wtsi | C57BL/6N-Smoc1tm1a(EUCOMM)Wtsi | J:174198 | View | ||||
microphthalmia with limb anomalies | \Smoc1Tn(sb-lacZ,GFP)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 | ||||
mucosulfatidosis | \Sumf1Gt(RST760)Byg/\Sumf1Gt(RST760)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:120146 | View | ||||
mulibrey nanism | \Trim37Gt(RRO307)Byg/\Trim37Gt(RRO307)Byg | B6J.129P2-Trim37Gt(RRO307)Byg | J:232482 | 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 | ||||
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 | ||||
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 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 1 | \Nphp1em1Ssau/\Nphp1em1Ssau | C57BL/6J-Nphp1em1Ssau | J:360848 | 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 |
\Spink5tm1Hov/\Spink5tm2.1Hov \Tg(KRT5-cre/ERT2)2Ipc/0 |
involves: 129P2/OlaHsd * C57BL/6 * C57BL/6JRj * SJL | J:357366 | View | ||||
Netherton syndrome |
\Spink5tm2.1Hov/\Spink5tm2.1Hov \Tg(KRT5-cre/ERT2)2Ipc/0 |
involves: C57BL/6 * C57BL/6JRj * SJL | J:357366 | View | ||||
Netherton syndrome | \Spink5Tn(Pgk2-sb10,sb-Tyr)1498Ove/\Spink5Tn(Pgk2-sb10,sb-Tyr)1498Ove | involves: FVB/N | J:93050 | View | ||||
neurodegeneration with brain iron accumulation 2a | \Pla2g6m1J/\Pla2g6m1J | C3H/HeJ-Pla2g6m1J | J:183152 | View | ||||
neurodegeneration with brain iron accumulation 2a | \Pla2g6m1Sein/\Pla2g6m1Sein | C57BL/6JJcl-Pla2g6m1Sein | J:155328 | View | ||||
neurodegeneration with brain iron accumulation 2a | \Pla2g6tm1Tsu/\Pla2g6tm1Tsu | involves: 129S2/SvPas * C57BL/6 | J:174587 | View | ||||
neurodegeneration with brain iron accumulation 2a | \Pla2g6tm1Turk/\Pla2g6tm1Turk | involves: 129X1/SvJ | J:131429 | View | ||||
neurodegeneration with brain iron accumulation 6 |
\Coasytm1.1Vtr/\Coasytm1.1Vtr \Tg(Syn1-cre)671Jxm/0 |
involves: 129 * C57BL/6N * CBA | J:299154 | View | ||||
neurodevelopmental disorder with midbrain and hindbrain malformations | \Arhgef2Gt(IST13976A8)Tigm/\Arhgef2Gt(IST13976A8)Tigm | involves: C57BL/6N | J:242973 | 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:12816, 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 | ||||
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 | ||||
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 | ||||
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 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 14 | \Pla2g6tm1.1Hlw/\Pla2g6tm1.1Hlw | involves: 129 * C57BL/6J | J:317126 | 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 | ||||
PHARC syndrome | \Abhd12tm1Crv/\Abhd12tm1Crv | involves: C57BL/6 | J:193716 | View | ||||
Pierson syndrome | \Lamb2npht/\Lamb2npht | involves: C57BL/6 | J:208069 | View | ||||
Pierson syndrome | \Lamb2tm1Jrs/\Lamb2tm1Jrs | involves: 129S1/Sv * 129X1/SvJ | J:106005 | 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 | ||||
polycystic kidney disease 4 | \Pkhd1em1Mrug/\Pkhd1+ | involves: C57BL/6J | J:281464 | View | ||||
polycystic kidney disease 4 | \Pkhd1em1Mrug/\Pkhd1em1Mrug | involves: C57BL/6J | J:281464 | 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 | ||||
primary autosomal recessive microcephaly 2 with or without cortical malformations | \Wdr62tm1.1Jfch/\Wdr62tm1.1Jfch | involves: 129S1/SvImJ * C57BL/6N | J:282438 | 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 | ||||
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 | ||||
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 | ||||
retinitis pigmentosa 1 | \Rp1m1Jdun/\Rp1m1Jdun | C57BL/6-Rp1m1Jdun | J:214837 | View | ||||
retinitis pigmentosa 1 | \Rp1tm1Jnz/\Rp1tm1Jnz | involves: 129S7/SvEvBrd | J:76071 | 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 12 | \Crb1tm1Wij/\Crb1tm2Wij | involves: 129P2/OlaHsd * C57BL/6 | J:117415 | View | ||||
retinitis pigmentosa 14 | \Tulp1tm1Pjn/\Tulp1tm1Pjn | involves: 129X1/SvJ * C57BL/6 | J:59884 | 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 | ||||
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 | ||||
Schimke immuno-osseous dysplasia | \Smarcal1tm1.1Cfbo/\Smarcal1tm1.1Cfbo | either: B6.129-Smarcal1tm1.1Cfbo or (involves: 129 * C57BL/6) | J:183899 | 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 | ||||
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-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 | ||||
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 | ||||
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 with axonal neuropathy 1 | \Tdp1Gt(XD105)Byg/\Tdp1Gt(XD105)Byg | involves: 129P2/OlaHsd * C57BL/6 | J:127605 | 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 | ||||
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 | ||||
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 | ||||
Troyer syndrome | \Sparttm1.1Xen/\Sparttm1.1Xen | involves: C57BL/6J | J:185987 | 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 | ||||
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 | ||||
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 | ||||
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 | \Lipatm1Hodu/\Lipatm1Hodu | involves: 129P2/OlaHsd * CF-1 | J:49674 | 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 | ||||
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 | ||||
![]() | 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 | ||||
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 | ||||
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 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 | ||||
Bardet-Biedl syndrome | \Tbc1d32b2b2284Clo/\Tbc1d32b2b2284Clo | C57BL/6J-Tbc1d32b2b2284Clo | J:175213 | View | ||||
beta thalassemia | \Klf1tm1Sho/\Klf1tm1Sho | involves: 129S4/SvJae * C57BL/6 | J:25651 | View | ||||
Bloom syndrome |
\Nsmce2tm2.1Ofc/\Nsmce2tm2.1Ofc \Ndor1Tg(UBC-cre/ERT2)1Ejb/0 |
involves: 129S/SvEv * C57BL/6 * SJL | J:227197 | View | ||||
Canavan disease | \Sod2tm1Cje/\Sod2tm1Cje | involves: C57BL/6J | J:45913 | View | ||||
Caroli syndrome | \Pkhd1cyli/\Pkhd1cyli | D2.Cg-(D4Mit42-D4Smh6b) Pkhd1cyli/EiJ | J:343537 | View | ||||
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome | \Atp8a2wl-3J/\Atp8a2wl-3J | CBA/J-Atp8a2wl-3J/J | J:222308 | View | ||||
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome | \Atp8a2wl-vmd/\Atp8a2wl-vmd | C3H/HeSnJ-Atp8a2wl-vmd/J | J:222308 | View | ||||
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome | \Atp8a2wl/\Atp8a2wl | involves: C57BL/6J | J:222308 | View | ||||
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome | \Atp8a2wl/\Atp8a2wl | Not Specified | J:222308 | View | ||||
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome | \Car8wdl/\Car8wdl | C57BLKS/J-Car8wdl/GrsrJ | J:230904 | View | ||||
Charlevoix-Saguenay spastic ataxia | \Ankfy1Gt(RRE069)Byg/\Ankfy1+ | B6.129P2-Ankfy1Gt(RRE069)Byg | J:250135 | 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 | ||||
congenital amegakaryocytic thrombocytopenia | \Mpltm1Fjs/\Mpltm1Fjs | involves: 129 * C57BL/6J | J:87416 | 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 | ||||
cystic fibrosis | \Tg(Scgb1a1-Scnn1b)6608Bouc/0 | involves: C3H * C57BL/6 | J:91139 | View | ||||
enhanced S-cone syndrome | \Nrltm1Asw/\Nrltm1Asw | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:175566 | 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 | \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 | ||||
glycine encephalopathy | \Slc6a9tm1Betz/\Slc6a9tm1Betz | involves: 129P2/OlaHsd * C57BL/6 | J:86624 | 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 | ||||
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 | ||||
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 | ||||
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 | ||||
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 | ||||
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 | ||||
lysosomal acid lipase deficiency | \Lipatm1Hodu/\Lipatm1Hodu | involves: 129P2/OlaHsd * CF-1 | J:49674 | View | ||||
microvillus inclusion disease |
\Cdc42tm1Brak/\Cdc42tm1Brak \Tg(Vil1-cre)997Gum/0 |
involves: C57BL/6J * SJL | J:184563 | View | ||||
mitochondrial DNA depletion syndrome 3 | \Mpv17/\Mpv17 | CFW-Mpv17/J | J:143355 | 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 | ||||
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 | ||||
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 | ||||
Pendred Syndrome | \Foxi1tm1Sven/\Foxi1tm1Sven | involves: CD-1 | J:83207 | View | ||||
Pierson syndrome | \Tns2nph/\Tns2nph | involves: ICR | J:108691 | View | ||||
poor metabolism of thiopurines | \Tpmttm1Rlng/\Tpmttm1Rlng | involves: 129P2/OlaHsd * C57BL/6 * NMRI | J:121737 | 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 | ||||
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 | ||||
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 | \Cep63Gt(EUCE0251h11)Hmgu/\Cep63Gt(EUCE0251h11)Hmgu | involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6 | J:224364 | View | ||||
Seckel syndrome | \Cpaptm1a(EUCOMM)Wtsi/\Cpaptm1a(EUCOMM)Wtsi | B6Brd;B6N-Tyrc-Brd Cpaptm1a(EUCOMM)Wtsi/Wtsi | J:194085 | View | ||||
Senior-Loken syndrome | \Tmem218Gt(OST40451)Lex/\Tmem218Gt(OST40451)Lex | involves: 129S5/SvEvBrd * C57BL/6 | J:227399 | View | ||||
severe combined immunodeficiency 104 | \Coro1akoy/\Coro1akoy | C57BL/6-Coro1akoy | J:141431 | View | ||||
severe combined immunodeficiency 104 | \Coro1aptcd/\Coro1aptcd | B6.CTS-Coro1aptcd | J:141431 | View | ||||
severe combined immunodeficiency 104 | \Coro1aptcd/\Coro1atm1Achn | B6.Cg-Coro1aptcd Coro1atm1Achn | J:141431 | View | ||||
severe combined immunodeficiency 104 | \Coro1atm1Achn/\Coro1atm1Achn | B6.129X1-Coro1atm1Achn | J:141431 | View | ||||
severe combined immunodeficiency 104 | \Jak3tm1Ljb/\Jak3tm1Ljb | involves: 129S4/SvJae | J:64861 | View | ||||
severe combined immunodeficiency 104 | \Jak3tm1Tks/\Jak3tm1Tks | involves: 129P2/OlaHsd * C57BL/6 | J:31231 | View | ||||
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive | \Prkdcscid/\Prkdcscid | C.BKa-Prkdcscid | J:6958 | 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 | ||||
thalassemia | \Ppp1r15atm1.1Ajf/\Ppp1r15atm1.1Ajf | involves: 129 * C57BL/6 | J:106905 | 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 | ||||
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 | ||||
Walker-Warburg syndrome | \Col4a1deltaex40/\Col4a1+ | involves: 129S/SvEv * C57BL/6J | J:172720 | 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 | ||||
![]() | 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 | ||||
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 | ||||
Griscelli syndrome type 2 |
\a/\a \Rab27aash/\Rab27aash |
involves: C3H/HeSnJ * C57BL/6J | J:77395 | 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 | ||||
mitochondrial DNA depletion syndrome 1 |
\Tymptm1Mihi/\Tymptm1Mihi \Upp1tm1Gp/\Upp1tm1Gp |
involves: 129 * 129X1/SvJ * C57BL/6J | J:144245 | 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 | ||||
Wolfram syndrome 2 | \Cisd2tm1Tfts/\Cisd2tm1Tfts | B6.129S7-Cisd2tm1Tfts | J:148467 | View | ||||
Transgenes and Other Mutations | alpha thalassemia | \Hbatm1Ney/\Hbatm1Ney | either: (involves: 129P2/OlaHsd) or (involves: 129X1/SvJ) | J:86682 | 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 | ||||
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 | ||||
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 | ||||
congenital generalized lipodystrophy type 2 | \Tg(aP2-SREBF1c)9884Reh/0 | involves: C57BL/6J * SJL | J:50770 | 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 | ||||
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 | ||||
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 | ||||
Parkinson's disease 2 | \Tg(Slc6a3-PARK2*Q311X)AXwy/0 | FVB/NJ-Tg(Slc6a3-PARK2*Q311X)AXwy | J:146833 | 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 | ||||
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 | ||||
Werner syndrome | \Tg(CAG-WRN*K577M)5025Wcl/0 | involves: C3H * C57BL/6J | J:95127 | View | ||||
Additional Complex Models | 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 | ||||
Ehlers-Danlos syndrome spondylodysplastic type 2 |
\Bgntm1Mfy/Y \Dcntm1Ioz/\Dcntm1Ioz |
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ | J:91512 | View | ||||
Hermansky-Pudlak syndrome |
\Rab32tm1b(KOMP)Wtsi/\Rab32tm1b(KOMP)Wtsi \Rab38tm1.1Ics/\Rab38tm1.1Ics |
involves: C57BL/6N * C57BL/6NTac | J:293385 | View |
No similarity to the expected human disease phenotype was found.
|
||||||||
Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
NOT Models | achromatopsia 2 | \Cnga3cpfl5/\Cnga3tm1Eye | involves: 129S6/SvEvTac * C57BL/6J * RHJ/LeJ | J:358897 | View | |||
achromatopsia 2 | \Cnga3em1Eye/\Cnga3em1Eye | C57BL/6J-Cnga3em1Eye | J:358897 | View | ||||
achromatopsia 2 | \Cnga3tm1Eye/\Cnga3tm1Eye | involves: 129S6/SvEvTac * C57BL/6J | J:358897 | 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 | ||||
Charcot-Marie-Tooth disease type 2B1 | \Lmnatm1.1Vde/\Lmnatm1.1Vde | B6.129(Cg)-Lmnatm1.1Vde | J:322912 | 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 | ||||
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 | ||||
Fanconi anemia complementation group P | \Slx4tm1.2Jrou/\Slx4tm1.2Jrou | B6.129P2-Slx4tm1.2Jrou | J:204996 | View | ||||
Fraser syndrome | \Frem3em1Osb/\Frem3em1Osb | involves: C57BL/6NJcl * DBA/2NJcl | J:291067 | 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 | ||||
Leber congenital amaurosis 9 | \Nmnat1tm1Ruch/\Nmnat1tm1Ruch | involves: 129S7/SvEvBrd | J:267630 | 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 | ||||
nephronophthisis 1 | \Nphp1tm1.1Hung/\Nphp1tm1.1Hung | B6.Cg-Nphp1tm1.1Hung | J:140205 | View | ||||
pantothenate kinase-associated neurodegeneration | \Pank2tm1Jgt/\Pank2tm1Jgt | involves: 129X1/SvJ * C57BL/6J | J:94753 | 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 | ||||
triple-A syndrome | \Aaastm1Ahue/\Aaastm1Ahue | involves: 129P2/OlaHsd * C57BL/6 | J:106908 | View | ||||
Usher syndrome type 1J | \Cib2tm1.1Aela/\Cib2tm1.1Aela | involves: BALB/c * C57BL/6 * C57BL/6N | J:262464 | View |