Excel File Text File All mouse models of autosomal recessive disease with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      2-aminoadipic 2-oxoadipic aciduria Dhtkd1em1Hpr/Dhtkd1em1Hpr involves: C57BL/6N * FVB/N J:256227 View
3-methylglutaconic aciduria type 3 Opa3m1Votr/Opa3m1Votr involves: C3H * C57BL/6JCrl J:181670, J:188346 View
3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome Serac1em1Bcgen/Serac1em1Bcgen C57BL/6N-Serac1em1Bcgen J:326672 View
17-beta hydroxysteroid dehydrogenase 3 deficiency Hsd17b3tm1.2Mpo/Hsd17b3tm1.2Mpo involves: 129S6/SvEvTac * C57BL/6N * C57BL/6NCrl J:301756 View
aceruloplasminemia 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 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 1A Del(14Gjb6-Cryl1)1Lmon/Del(14Gjb6-Cryl1)1Lmon C57BL/6JOlaHsd-Del(14Gjb6-Cryl1)1Lmon/Lmon J:345081 View
autosomal recessive nonsyndromic deafness 1A Gjb2tm1Ugds/Gjb2tm1Ugds
Tg(Otog-cre)1Ugds/0		 involves: 129P2/OlaHsd * C57BL/6 J:77823 View
autosomal recessive nonsyndromic deafness 1A Gjb2tm1Ugds/Gjb2tm1Ugds
Tg(Sox10-cre)1Wdr/0		 involves: 129P2/OlaHsd * C57BL/6 * CBA J:206835 View
autosomal recessive nonsyndromic deafness 1A Gjb6tm1.1Fama/Gjb6tm1.1Fama involves: 129P2/OlaHsd * C57BL/6 * SJL J:166362 View
autosomal recessive nonsyndromic deafness 1A Gjb6tm1Kwi/Gjb6tm1Kwi involves: 129P2/OlaHsd * C57BL/6 J:80917 View
autosomal recessive nonsyndromic deafness 2 Myo7admbo2/Myo7admbo2 involves: C57BL/6J J:195666 View
autosomal recessive nonsyndromic deafness 3 Myo15ash2-2J/Myo15ash2-2J involves: STOCK Rb(16.17)7Bnr J:69998 View
autosomal recessive nonsyndromic deafness 3 Myo15atm1.1Jebd/Myo15atm1.1Jebd involves: C57BL/6 * FVB/N J:226820 View
autosomal recessive nonsyndromic deafness 7 Tmc1baringo/Tmc1baringo involves: C57BL/6 J:181985 View
autosomal recessive nonsyndromic deafness 7 Tmc1dn/Tmc1dn involves: STOCK Grhl3ct * M. m. molossinus J:22445 View
autosomal recessive nonsyndromic deafness 7 Tmc1dn/Tmc1dn STOCK Grhl3ct/J J:236 View
autosomal recessive nonsyndromic deafness 7 Tmc1Mhdabth/Tmc1+ C3HeB/FeJ-Tmc1Mhdabth/Ieg J:86685 View
autosomal recessive nonsyndromic deafness 7 Tmc1nice/Tmc1nice involves: C57BL/6 J:181985 View
autosomal recessive nonsyndromic deafness 7 Tmc1stitch/Tmc1stitch involves: C57BL/6 J:181985 View
autosomal recessive nonsyndromic deafness 9 Otofdeaf5Jcs/Otofdeaf5Jcs STOCK Otofdeaf5Jcs/Kjn J:125960 View
autosomal recessive nonsyndromic deafness 9 Otoftm1Ugds/Otoftm1Ugds involves: 129S2/SvPas * C57BL/6 J:116097 View
autosomal recessive nonsyndromic deafness 12 Cdh2312J/Cdh2312J involves: C57BL/6J J:174758 View
autosomal recessive nonsyndromic deafness 12 Cdh23Jera/Cdh23Jera involves: C57BL/6 J:174130 View
autosomal recessive nonsyndromic deafness 12 Cdh23sals/Cdh23sals involves: C57BL/6J J:147149 View
autosomal recessive nonsyndromic deafness 16 Strctm1Ugds/Strctm1Ugds involves: 129S2/SvPas * BALB/c * C57BL/6 * C57BL/6J J:141421 View
autosomal recessive nonsyndromic deafness 18A Ush1cdfcr-2J/Ush1cdfcr-2J B6;129S4 J:85400 View
autosomal recessive nonsyndromic deafness 18A Ush1cdfcr-4J/Ush1cdfcr-4J 129P3/J-Ush1cdfcr-4J/J J:278662 View
autosomal recessive nonsyndromic deafness 18A Ush1cdfcr/Ush1cdfcr involves: BALB/cByJ J:85400 View
autosomal recessive nonsyndromic deafness 18B Otogvbd/Otogvbd involves: C3HeB/FeJ * C57BL/6J J:234038 View
autosomal recessive nonsyndromic deafness 22 Otoatm1Gpr/Otoatm1Gpr involves: 129S/SvEv J:192263 View
autosomal recessive nonsyndromic deafness 23 Pcdh15roda/Pcdh15roda BALB/c-Pcdh15roda J:220658 View
autosomal recessive nonsyndromic deafness 28 Triobptm1Tbf/Triobptm1Tbf C57BL/6-Triobptm1Tbf J:167947 View
autosomal recessive nonsyndromic deafness 29 Cldn14tm1Tbf/Cldn14tm1Tbf involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:85071 View
autosomal recessive nonsyndromic deafness 30 Myo3atm1.1Mckg/Myo3atm1.1Mckg C57BL/6-Myo3atm1.1Mckg J:166812 View
autosomal recessive nonsyndromic deafness 31 Whrnwi/Whrnwi involves: C57BL/6J * STOCK a Tyrp1b Myo5ad Oca2p Ednrbs J:269, J:5037, J:5538, J:77939 View
autosomal recessive nonsyndromic deafness 32 Cdc14aem1Tbf/Cdc14aem1Tbf involves: C57BL/6J J:257652 View
autosomal recessive nonsyndromic deafness 32 Cdc14atm1a(EUCOMM)Hmgu/Cdc14atm1b(EUCOMM)Hmgu involves: C57BL/6N * FVB J:257652 View
autosomal recessive nonsyndromic deafness 32 Cdc14atm1b(EUCOMM)Hmgu/Cdc14atm1b(EUCOMM)Hmgu involves: C57BL/6N * FVB J:257652 View
autosomal recessive nonsyndromic deafness 32 Cdc14atm1d(EUCOMM)Hmgu/Cdc14atm1d(EUCOMM)Hmgu involves: C57BL/6N * FVB J:257652 View
autosomal recessive nonsyndromic deafness 37 Myo6sv/Myo6sv involves: B10.HA/(33NX)Sn * C57BL/6J J:29898 View
autosomal recessive nonsyndromic deafness 39 Hgftm1.1Tbf/Hgftm1.1Tbf B6.Cg-Hgftm1.1Tbf/Tbf J:289982 View
autosomal recessive nonsyndromic deafness 39 Hgftm1Tbf/Hgftm1Tbf B6.Cg-Hgftm1Tbf/Tbf J:289982 View
autosomal recessive nonsyndromic deafness 42 Ildr1Gt(D178D03)Wrst/Ildr1Gt(D178D03)Wrst involves: 129S2/SvPas * Swiss Webster J:217755 View
autosomal recessive nonsyndromic deafness 42 Ildr1tm1(KOMP)Wtsi/Ildr1tm1(KOMP)Wtsi involves: C57BL/6N J:217755, J:221592 View
autosomal recessive nonsyndromic deafness 42 Ildr1tm1.1Lwa/Ildr1tm1.1Lwa involves: 129S6/SvEvTac * C57BL/6 J:221594 View
autosomal recessive nonsyndromic deafness 48 Cib2tm1.1Aela/Cib2tm1.1Aela involves: BALB/c * C57BL/6 * C57BL/6N J:262464 View
autosomal recessive nonsyndromic deafness 49 Marveld2tm1.1Sria/Marveld2tm1.1Sria involves: 129X1/SvJ * C57BL/6J J:201580 View
autosomal recessive nonsyndromic deafness 49 Marveld2tm1Sats/Marveld2tm1Sats B6.Cg-Marveld2tm1Sats J:261357 View
autosomal recessive nonsyndromic deafness 59 Pjvktm1Ugds/Pjvktm1Ugds involves: 129S2/SvPas * BALB/c * C57BL/6 J:111260 View
autosomal recessive nonsyndromic deafness 63 Tomtm1Btlr/Tomtm1Btlr C57BL/6J-Tomtm1Btlr J:137493 View
autosomal recessive nonsyndromic deafness 68 S1pr2stdf/S1pr2stdf involves: C57BL/6Brd * C57BL/6N J:240361 View
autosomal recessive nonsyndromic deafness 68 S1pr2tm1Ajml/S1pr2tm1Ajml either: (involves: 129S5/SvEvBrd) or (involves: 129S5/SvEvBrd * C57BL/6) J:231927 View
autosomal recessive nonsyndromic deafness 74 Msrb3tm1Hyk/Msrb3tm1Hyk involves: 129 * C57BL/6 J:206322 View
autosomal recessive nonsyndromic deafness 79 Tprnem1Pghu/Tprnem1Pghu B6.Cg-Tprnem1Pghu J:240563 View
autosomal recessive nonsyndromic deafness 88 Elmod3em1Jili/Elmod3em1Jili involves: C57BL/6 J:293683 View
autosomal recessive nonsyndromic deafness 93 Cabp2tm1b(KOMP)Mbp/Cabp2tm1b(KOMP)Mbp involves: C57BL/6N * FVB/N J:255028 View
autosomal recessive osteopetrosis 1 Tcirg1oc/Tcirg1oc B6C3Fe a/a-Tcirg1oc/J J:61295 View
autosomal recessive osteopetrosis 1 Tcirg1tm1Ypl/Tcirg1tm1Ypl involves: 129S4/SvJae * C57BL/6J J:58795 View
autosomal recessive osteopetrosis 2 Tnfsf11gum/Tnfsf11gum STOCK Tnfsf11gum/GrsrJ J:223062 View
autosomal recessive osteopetrosis 2 Tnfsf11tles/Tnfsf11tles involves: 129S6/SvEvTac * C57BL/6J J:179743 View
autosomal recessive osteopetrosis 2 Tnfsf11tm1Ywc/Tnfsf11tm1Ywc involves: 129P2/OlaHsd J:233265 View
autosomal recessive osteopetrosis 3 Car2n/Car2n involves: C57BL/6J * DBA/2J J:19268 View
autosomal recessive osteopetrosis 4 Clcn7tm1Tjj/Clcn7tm1Tjj involves: 129P2/OlaHsd * C57BL/6 J:67273 View
autosomal recessive osteopetrosis 4 Clcn7tm2Tjj/Clcn7tm2Tjj involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:67273 View
autosomal recessive osteopetrosis 5 Ostm1gl/Ostm1gl GL/Le Edardl-J +/+ Ostm1gl/J J:5561 View
autosomal recessive osteopetrosis 6 Ctsktm1(cre)Ska/Ctsk+
Plekhm1tm1.1Hzhao/Plekhm1tm1.1Hzhao		 involves: C57BL/6J * C57BL/6NCrlj * CBA/JNCrlj J:236517 View
autosomal recessive osteopetrosis 6 Plekhm1tm1.2Hzhao/Plekhm1tm1.2Hzhao involves: 129S1/Sv * C57BL/6J J:236517 View
autosomal recessive osteopetrosis 8 Snx10em1Ael/Snx10em1Ael involves: 129 * C57BL/6J * C57BL/6JOlaHsd J:289051 View
autosomal recessive osteopetrosis 8 Snx10em2Ael/Snx10em2Ael involves: 129 * C57BL/6J * C57BL/6JOlaHsd J:289051 View
autosomal recessive polycystic kidney disease Pkhd1tm1.1Ggg/Pkhd1tm1.1Ggg involves: 129S/SvEv * 129S4/SvJae * C57BL/6 J:125113 View
autosomal recessive polycystic kidney disease Pkhd1tm1Cjwa/Pkhd1tm1Cjwa involves: 129S6/SvEvTac * FVB/N J:140302 View
autosomal recessive polycystic kidney disease Pkhd1tm1Gwu/Pkhd1tm1Gwu involves: C57BL/6 J:167782 View
autosomal recessive polycystic kidney disease Pkhd1tm1Gwu/Pkhd1tm1Gwu Not Specified J:143394 View
autosomal recessive polycystic kidney disease Pkhd1tm1Sswi/Pkhd1tm1Sswi B6.Cg-Pkhd1tm1Sswi J:186064 View
autosomal recessive polycystic kidney disease Pkhd1tm2Cjwa/Pkhd1tm2Cjwa either: B6.129(Cg)-Pkhd1tm2Cjwa or C.129(Cg)-Pkhd1tm2Cjwa J:187735 View
autosomal recessive Robinow syndrome Ror2tm1Anec/Ror2tm1Anec B6.129S1-Ror2tm1Anec J:134490 View
autosomal recessive Robinow syndrome Ror2tm1Ymi/Ror2tm1Ymi involves: 129P2/OlaHsd * C57BL/6 J:88955 View
autosomal recessive spinocerebellar ataxia 12 Wwoxem1Mald/Wwoxem1Mald FVB/N-Wwoxem1Mald J:339564 View
autosomal recessive spinocerebellar ataxia 13 Grm1crv4/Grm1crv4 BALB/cPas-Grm1crv4 J:112290 View
autosomal recessive spinocerebellar ataxia 16 Stub1tm1Cpat/Stub1tm1Cpat involves: 129S/SvEv * C57BL/6 J:245069 View
autosomal recessive spinocerebellar ataxia 18 Grid2ho-15J/Grid2ho-15J involves: C3HeB/Fe J:220519 View
autosomal recessive spinocerebellar ataxia 18 Grid2tm1(cre)Mwa/Grid2tm1(cre)Mwa involves: C57BL/6N J:220519 View
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 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 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-icre)29066/2Sig/0		 involves: 129S2/SvPas * C57BL/6J * SJL J:238264 View
glycogen storage disease Ia G6pc1tm1Jyc/G6pc1tm1Jyc involves: 129S4/SvJae J:33212 View
glycogen storage disease Ia G6pc1tm2.2Jyc/G6pc1tm2.2Jyc involves: 129S4/SvJae * 129S4/SvJaeSor * C57BL/6J * FVB/N J:155990 View
glycogen storage disease II Gaatm1.1Rabn/Gaatm1.1Rabn involves: 129X1/SvJ * C57BL/6 * FVB/N J:76435 View
glycogen storage disease II Gaatm1Rabn/Gaatm1Rabn involves: 129X1/SvJ * C57BL/6 J:48839, J:76435 View
glycogen storage disease II Gaatm1Rabn/Gaatm1Rabn
Tg(CMV-GAA*P545L)#Kjv/0		 involves: 129X1/SvJ * C57BL/6 J:219022 View
glycogen storage disease II Gaatm1Vdp/Gaatm1Vdp either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * FVB) J:45386 View
glycogen storage disease II Gaatm2Rabn/Gaatm2Rabn involves: 129X1/SvJ * C57BL/6 J:76435 View
glycogen storage disease III Agltm1a(EUCOMM)Wtsi/Agltm1a(EUCOMM)Wtsi involves: C57BL/6N J:212003 View
glycogen storage disease III Agltm1Geno/Agltm1Geno C57BL/6J-Agltm1Geno J:218471 View
glycogen storage disease IV Gbe1m1Yty/Gbe1m1Yty C3HeB/FeJ-Gbe1m1Yty J:167233 View
glycogen storage disease IV Gbe1tm1.1Hoa/Gbe1tm1.1Hoa involves: 129S7/SvEvBrd J:176889 View
glycogen storage disease IV Gbe1tm1Hoa/Gbe1tm1Hoa involves: 129S7/SvEvBrd J:176889 View
glycogen storage disease IV Gbe1tm2.1Hoa/Gbe1tm2.1Hoa involves: 129S7/SvEvBrd J:226481 View
glycogen storage disease 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
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 Prss56glcr4/Prss56glcr4 C3A.Cg-Prss56glcr4 Pde6b+ J:188765 View
isolated microphthalmia 6 Prss56glcr4/Prss56glcr4 C57BL/6J-Prss56glcr4 J:188765 View
isolated microphthalmia 6 Prss56glcr4/Prss56glcr4 involves: C3H/HeA * C57BL/6J * C57BL/LiA J:188765 View
Johanson-Blizzard syndrome Ubr1tm1Avar/Ubr1tm1Avar involves: 129S1/Sv * C57BL/6 J:105229 View
junctional epidermolysis bullosa with pyloric atresia Itgb4tm1Fgg/Itgb4tm1Fgg involves: 129S1/Sv * C57BL/6 J:48924 View
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 2 Invsinv/Invsinv involves: FVB/N J:132552 View
nephronophthisis 3 Nphp3pcy/Nphp3pcy involves: KK J:91453 View
nephronophthisis 3 Nphp3pcy/Nphp3tm1Cbe involves: C57BL/6 * CD-1 * KK/Upj J:139258 View
nephronophthisis 4 Nphp4nmf192/Nphp4nmf192 involves: C57BL/6J J:167232 View
nephronophthisis 7 Glis2tm1Tre/Glis2tm1Tre B6.129P2-Glis2tm1Tre J:123510 View
Netherton syndrome F2rl1tm1Cgh/F2rl1tm1Cgh
Spink5tm1Hov/Spink5tm1Hov		 involves: 129P2/OlaHsd * 129S4/SvJae J:180855 View
Netherton syndrome Spink5m1Btlr/Spink5m1Btlr involves: C57BL/6J J:183755 View
Netherton syndrome Spink5tm1Drh/Spink5tm1Drh involves: 129P2/OlaHsd * C57BL/6 J:95549 View
Netherton syndrome Spink5tm1Hov/Spink5tm1Hov involves: 129P2/OlaHsd * FVB J:96435 View
Netherton syndrome Spink5Tn(Pgk2-sb10,sb-Tyr)1498Ove/Spink5Tn(Pgk2-sb10,sb-Tyr)1498Ove involves: FVB/N J:93050 View
neurodegeneration with brain iron accumulation 2a Pla2g6m1J/Pla2g6m1J C3H/HeJ-Pla2g6m1J J:183152 View
neurodegeneration with brain iron accumulation 2a Pla2g6m1Sein/Pla2g6m1Sein C57BL/6JJcl-Pla2g6m1Sein J:155328 View
neurodegeneration with brain iron accumulation 2a Pla2g6tm1Tsu/Pla2g6tm1Tsu involves: 129S2/SvPas * C57BL/6 J:174587 View
neurodegeneration with brain iron accumulation 2a Pla2g6tm1Turk/Pla2g6tm1Turk involves: 129X1/SvJ J:131429 View
neurodegeneration with brain iron accumulation 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: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
poor metabolism of thiopurines Tpmttm1Rlng/Tpmttm1Rlng involves: 129P2/OlaHsd * C57BL/6 * NMRI J:121737 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
pyruvate kinase deficiency of red cells Pklrchar4/Pklrchar4 involves: A/J * C57BL/6 J:86735 View
pyruvate kinase deficiency of red cells Pklrslc/Pklrslc CBA/NSlc-Pklrslc J:29199 View
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 1 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 Frem2my/Frem2my MY/HuLeJ J:111788 View
Fraser syndrome Frem2ne/Frem2ne STOCK Frem2ne/GrsrJ J:185265, J:222308 View
Fraser syndrome Grip1eb/Grip1eb involves: ATEB/Le * C57BL/6J J:111788 View
Fraser syndrome Grip1tm1Rha/Grip1tm1Rha B6.129-Grip1tm1Rha J:88266 View
Gitelman syndrome Stk39tm1.2Slin/Stk39tm1.2Slin involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:165706 View
Gitelman syndrome Stk39tm1Pawe/Stk39tm1Pawe involves: 129S6/SvEvTac * C57BL/6J J:287773 View
Gitelman syndrome Stk39tm2.1Arte/Stk39tm2.1Arte involves: C57BL/6J J:224087 View
Gitelman syndrome Wnk4tm1Pfi/Wnk4tm1Pfi involves: 129S6/SvEvTac * C57BL/6J J:184790 View
glycine encephalopathy Slc6a9tm1Betz/Slc6a9tm1Betz involves: 129P2/OlaHsd * C57BL/6 J:86624 View
glycogen storage disease Ia Slc37a4tm1Jyc/Slc37a4tm1Jyc involves: 129S4/SvJae * C57BL/6 J:86005 View
glycogen storage disease V Hif1atm3Rsjo/Hif1atm3Rsjo
Tg(Ckmm-cre)5Khn/?		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N J:97761 View
glycogen storage disease VII Hif1atm3Rsjo/Hif1atm3Rsjo
Tg(Ckmm-cre)5Khn/?		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6J * FVB/N J:97761 View
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
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 Cenpjtm1a(EUCOMM)Wtsi/Cenpjtm1a(EUCOMM)Wtsi B6Brd;B6N-Tyrc-Brd Cenpjtm1a(EUCOMM)Wtsi/Wtsi J:194085 View
Seckel syndrome Cep63Gt(EUCE0251h11)Hmgu/Cep63Gt(EUCE0251h11)Hmgu involves: 129P2/OlaHsd * 129S/SvEv * C57BL/6 J:224364 View
Senior-Loken syndrome Tmem218Gt(OST40451)Lex/Tmem218Gt(OST40451)Lex involves: 129S5/SvEvBrd * C57BL/6 J:227399 View
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-negative, Nk cell-positive Prkdcscid/Prkdcscid C.BKa-Prkdcscid J:6958 View
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive Coro1akoy/Coro1akoy C57BL/6-Coro1akoy J:141431 View
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive Coro1aptcd/Coro1aptcd B6.CTS-Coro1aptcd J:141431 View
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive Coro1aptcd/Coro1atm1Achn B6.Cg-Coro1aptcd Coro1atm1Achn J:141431 View
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive Coro1atm1Achn/Coro1atm1Achn B6.129X1-Coro1atm1Achn J:141431 View
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive Jak3tm1Ljb/Jak3tm1Ljb involves: 129S4/SvJae J:64861 View
severe combined immunodeficiency, autosomal recessive, T cell-negative, B cell-positive, Nk cell-positive Jak3tm1Tks/Jak3tm1Tks involves: 129P2/OlaHsd * C57BL/6 J:31231 View
sickle cell anemia Spta1sph-ha/Spta1sph-ha either: (B6.D1-Spta1sph-ha x WB.D1-Spta1sph-ha)F1 or (WB.D1-Spta1sph-ha x B6.D1-Spta1sph-ha)F1 J:12830 View
Smith-McCort dysplasia DymGt(GTR1.3)1Rul/DymGt(GTR1.3)1Rul involves: 129 J:141099 View
SOST-related sclerosing bone dysplasia Sosttm1(KOMP)Vlcg/Sosttm1(KOMP)Vlcg involves: C57BL/6NTac J:188586 View
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      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