Excel File Text File All mouse models of neuropathy with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      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
Becker muscular dystrophy Dmdmdx-3Cv/Y involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus J:23375 View
Bethlem myopathy Col6a1tm1Gmb/Col6a1tm1Gmb involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:51410, J:86734 View
Charcot-Marie-Tooth disease axonal type 2K Gdap1tm1.2Geno/Gdap1tm1.2Geno involves: 129 * C57BL/6 J:224701 View
Charcot-Marie-Tooth disease axonal type 2O Dync1h1tm1.1Sjki/Dync1h1+ involves: 129 * 129S1/SvImJ * C57BL/6 * C57BL/6J J:264493 View
Charcot-Marie-Tooth disease axonal type 2P Lrsam1Gt(RRK461)Byg/Lrsam1Gt(RRK461)Byg involves: 129P2/OlaHsd J:196447 View
Charcot-Marie-Tooth disease axonal type 2Q Dhtkd1tm1Mmgu/Dhtkd1tm1Mmgu involves: 129S6/SvEvTac * C57BL/6J J:288186 View
Charcot-Marie-Tooth disease axonal type 2Q Dhtkd1tm1Zgwg/Dhtkd1tm1Zgwg involves: C57BL/6 J:267178 View
Charcot-Marie-Tooth disease axonal type 2S Ighmbp2em1Cx/Ighmbp2em1Cx C57BL/6J-Ighmbp2em1Cx/Cx J:337488 View
Charcot-Marie-Tooth disease axonal type 2S Ighmbp2em5Cx/Ighmbp2em5Cx C57BL/6J-Ighmbp2em5Cx/Cx J:337488 View
Charcot-Marie-Tooth disease axonal type 2Z Morc2aem1Snupy/Morc2a+ involves: C57BL/6 J:341847 View
Charcot-Marie-Tooth disease dominant intermediate C Yars1tm1.1Rwb/Yars1tm1.1Rwb involves: C57BL/6N * FVB/N J:310162 View
Charcot-Marie-Tooth disease recessive intermediate D Cox6a1tm1(KOMP)Wtsi/Cox6a1tm1(KOMP)Wtsi involves: C57BL/6JJcl * C57BL/6N J:230212 View
Charcot-Marie-Tooth disease type 1A Pmp22Tr-2J/Pmp22+ C57BL/6J-Pmp22Tr-2J/GrsrJ J:201866 View
Charcot-Marie-Tooth disease type 1A Pmp22Tr-J/Pmp22+ B6.Cg-Pmp22Tr-J Krt25Re/+ +/J J:3394, J:101812 View
Charcot-Marie-Tooth disease type 1A Pmp22Tr-J/Pmp22+ involves: C57BL/6 J:3394, J:98231 View
Charcot-Marie-Tooth disease type 1A Tg(Pmp22)247Ueli/0 involves: C3H * C57BL/6 J:98118 View
Charcot-Marie-Tooth disease type 1A Tg(Pmp22)My41Clh/0 involves: C57BL/6J * CBA/Ca J:76795 View
Charcot-Marie-Tooth disease type 1A Tg(PMP22-tTA)JY13Clh/0
Tg(tetO/CMV-Pmp22)JP18Clh/0		 involves: C57BL/6J * CBA/Ca J:69545 View
Charcot-Marie-Tooth disease type 1B Mpztm1Msch/Mpz+ involves: 129S7/SvEvBrd J:42838 View
Charcot-Marie-Tooth disease type 1B Mpztm1Msch/Mpz+
Tg(Mpz*S63X)31Mes/0		 involves: 129S7/SvEvBrd * FVB/N J:105751 View
Charcot-Marie-Tooth disease type 1B Mpztm1Msch/Mpztm1Msch involves: 129S7/SvEvBrd J:42838 View
Charcot-Marie-Tooth disease type 1B Mpztm3.1Wra/Mpz+ FVB.129S2(Cg)-Mpztm3.1Wra J:241742 View
Charcot-Marie-Tooth disease type 1B Mpztm3.1Wra/Mpztm3.1Wra FVB.129S2(Cg)-Mpztm1.1Wra J:241742 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz)88.1Mfel/0 FVB/N-Tg(Mpz)88.1Mfel J:77658 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz)88.2Mfel/0 FVB/N-Tg(Mpz)88.2Mfel J:77658 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz)88.4Mfel/0 FVB/N-Tg(Mpz)88.4Mfel J:77658 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz*S63X)30Mes/0 involves: FVB/N J:105751 View
Charcot-Marie-Tooth disease type 1B Tg(Mpz*S63X)31Mes/0 involves: FVB/N J:105751 View
Charcot-Marie-Tooth disease type 1C Litaftm1.1Cwc/Litaftm1.1Cwc B6.Cg-Litaftm1.1Cwc J:314784 View
Charcot-Marie-Tooth disease type 1E Pmp22Tr-2J/Pmp22+ C57BL/6J-Pmp22Tr-2J/GrsrJ J:201866 View
Charcot-Marie-Tooth disease type 2A1 Kif1btm1Noh/Kif1b+ involves: 129S4/SvJae * C57BL/6J J:69772 View
Charcot-Marie-Tooth disease type 2A2A Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc/Tg(Mnx1-Mfn2*T105M,-EGFP)1Dcc Not Specified J:132035 View
Charcot-Marie-Tooth disease type 2B Rab7em2Rwb/Rab7+ C57BL/6J-Rab7em2Rwb/RwbJ J:346904 View
Charcot-Marie-Tooth disease type 2B1 Lmnatm1Stw/Lmnatm1Stw involves: 129S1/Sv J:75378 View
Charcot-Marie-Tooth disease type 2D Gars1C201R/Gars1+ involves: BALB/cAnN * C3H/HeH * C57BL/6J J:149830, J:179811 View
Charcot-Marie-Tooth disease type 2D Gars1em1Rwb/Gars1em2Rwb involves: C57BL/6NJ * FVB/NJ J:284948 View
Charcot-Marie-Tooth disease type 2D Gars1Nmf249/Gars1+ C57BL/6J-Gars1Nmf249/J J:112221 View
Charcot-Marie-Tooth disease type 2D Gars1Nmf249/Gars1+ involves: C57BL/6J * CAST/Ei J:179811 View
Charcot-Marie-Tooth disease type 2E Nefltm2.1Liem/Nefl+ B6.Cg-Nefltm2.1Liem J:220605 View
Charcot-Marie-Tooth disease type 3 Mpztm1Msch/Mpztm1Msch involves: 129S7/SvEvBrd J:42838 View
Charcot-Marie-Tooth disease type 3 Pmp22Tr-2J/Pmp22+ C57BL/6J-Pmp22Tr-2J/GrsrJ J:201866 View
Charcot-Marie-Tooth disease type 3 Tg(Mpz*S63C)32Mes/0 involves: FVB/N J:105751 View
Charcot-Marie-Tooth disease type 3 Tg(Mpz*S63C)33Mes/0 involves: FVB/N J:105751 View
Charcot-Marie-Tooth disease type 4B1 Mtmr2tm1.1Abol/Mtmr2tm1.1Abol involves: 129S2/SvPas J:94373 View
Charcot-Marie-Tooth disease type 4B1 Mtmr2tm1Ueli/Mtmr2tm1Ueli involves: 129S6/SvEvTac * C57BL/6 J:104120 View
Charcot-Marie-Tooth disease type 4B2 Sbf2Gt(RRF511)Byg/Sbf2Gt(RRF511)Byg involves: 129P2/OlaHsd * C57BL/6 J:133391 View
Charcot-Marie-Tooth disease type 4B2 Sbf2Gt(XH212)Byg/Sbf2Gt(XH212)Byg involves: 129P2/OlaHsd * C57BL/6 J:133042 View
Charcot-Marie-Tooth disease type 4B3 Sbf1em1Frobi/Sbf1em1Frobi C57BL/6N-Sbf1em1Frobi J:326685 View
Charcot-Marie-Tooth disease type 4C Sh3tc2tm1.1Rchr/Sh3tc2tm1.1Rchr involves: 129/Sv * FVB/N J:153705 View
Charcot-Marie-Tooth disease type 4D Ndrg1em1Lxli/Ndrg1em1Lxli C57BL/6N-Ndrg1em1Lxli J:330126 View
Charcot-Marie-Tooth disease type 4D Ndrg1tm1Myta/Ndrg1tm1Myta involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:89888 View
Charcot-Marie-Tooth disease type 4E Egr2tm1Jmi/Egr2tm1Jmi Not Specified J:96641 View
Charcot-Marie-Tooth disease type 4E Egr2tm2Jmi/Egr2tm2Jmi B6.Cg-Egr2tm2Jmi J:145949 View
Charcot-Marie-Tooth disease type 4H Fgd4tm1.1Ics/Fgd4tm1.1Ics Not Specified J:190437 View
Charcot-Marie-Tooth disease type 4J Fig4plt1/Fig4plt1 involves: 129P2/OlaHsd * C3H * C57BL/6 * CAST/Ei * SJL J:122737 View
Charcot-Marie-Tooth disease type 4J Fig4plt1/Fig4plt1
Tg(ACTB-Fig4*I41T)705Mm/0		 involves: 129 * C3H * C57BL/6J * CAST/Ei * SJL J:173446 View
Charcot-Marie-Tooth disease X-linked dominant 1 Gjb1tm1Kwi/Gjb1tm1Kwi involves: 129S4/SvJae J:40955 View
Charcot-Marie-Tooth disease X-linked dominant 1 Gjb1tm1Kwi/Gjb1tm1Kwi involves: 129S4/SvJae * C57BL/6 J:36146 View
Charcot-Marie-Tooth disease X-linked dominant 1 Gjb1tm1Kwi/Y involves: 129S4/SvJae J:40955 View
Charcot-Marie-Tooth disease X-linked dominant 1 Gjb1tm1Kwi/Y involves: 129S4/SvJae * C57BL/6 J:36146 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-2J/Lama2dy-2J B6.WK-Lama2dy-2J J:97464 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-6J/Lama2dy-6J involves: C57BL/6JEi * DBA/2J J:56803 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-7J/Lama2dy-7J C57BL/6J-Lama2dy-7J/J J:134367 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-8J/Lama2dy-8J C57BL/6J-Lama2dy-8J/GrsrJ J:149729 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy-Pas/Lama2dy-Pas involves: non-inbred stock J:102806 View
congenital merosin-deficient muscular dystrophy 1A Lama2dy/Lama2dy involves: 129P1/Re J:13125 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv J:170192 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv * Black Swiss J:59089 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Eeng/Lama2tm1Eeng involves: 129S1/Sv * Black Swiss * FVB/N J:49435 View
congenital merosin-deficient muscular dystrophy 1A Lama2tm1Stk/Lama2tm1Stk involves: 129/Sv * 129P2/OlaHsd * BALB/c * ICR J:43145, J:167230 View
congenital muscular dystrophy due to integrin alpha-7 deficiency Itga7tm1Umr/Itga7tm1Umr involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:82116 View
congenital muscular dystrophy due to LMNA mutation Lmnatm2.1Gbon/Lmnatm2.1Gbon involves: 129 * C57BL/6 J:180603 View
congenital myasthenic syndrome 3A Tg(Ckm-Chrnd*S262T)40Cgz/0 involves: C57BL/6 * DBA/2 J:31221 View
congenital myasthenic syndrome 4A Chrnetm2Vwi/Chrnetm2Vwi involves: 129P2/OlaHsd * C57BL/6 J:182046 View
congenital myasthenic syndrome 4A Tg(Ckm-Chrne*L269F)5Cgz/? involves: FVB/NJ J:193524 View
congenital myasthenic syndrome 4C Chrnetm1Vwi/Chrnetm1Vwi involves: 129P2/OlaHsd * C57BL/6 J:128178 View
congenital myasthenic syndrome 5 Colqtm1Jrs/Colqtm1Jrs involves: 129S1/Sv * 129X1/SvJ J:54006 View
congenital myasthenic syndrome 6 Chattm1.1Jrs/Chattm1.1Jrs Not Specified J:91066 View
congenital myasthenic syndrome 6 Chattm1Fhg/Chattm1Fhg involves: 129S2/SvPas * C57BL/6 J:81738 View
congenital myasthenic syndrome 8 Agrnnmf380/Agrnnmf380 C57BL/6J-Agrnnmf380/J J:176117 View
congenital myasthenic syndrome 9 Musktm1.1Vwi/Musktm2Vwi Not Specified J:141024 View
congenital myasthenic syndrome 9 Musktm1Vwi/Musktm1.1Vwi
Tg(Ckmm-cre)5Khn/0		 involves: C57BL/6J * FVB J:106867 View
congenital myasthenic syndrome 9 Musktm1Vwi/Musktm1Vwi
Tg(Ckmm-cre)5Khn/0		 involves: C57BL/6J * FVB J:106867 View
congenital myasthenic syndrome 10 Dok7tm2Yyam/Dok7tm2Yyam involves: 129P2/OlaHsd * C57BL/6J J:213767 View
congenital myasthenic syndrome 11 Rapsnem1Gan/Rapsnem1Gan C57BL/6J-Rapsnem1Gan J:282816 View
congenital myasthenic syndrome 12 Gfpt1tm1c(EUCOMM)Wtsi/Gfpt1tm1c(EUCOMM)Wtsi
Tg(Ckmm-cre)5Khn/0		 involves: C57BL/6J * C57BL/6N * SJL/J J:265013 View
congenital myasthenic syndrome 19 Col13a1tm3.1Pih/Col13a1tm3.1Pih involves: 129S1/Sv * 129X1/SvJ J:242846 View
congenital nystagmus 1 Frmd7tm1b(KOMP)Wtsi/Frmd7tm1b(KOMP)Wtsi involves: C57BL/6 * C57BL/6N J:299010 View
congenital nystagmus 1 Frmd7tm1b(KOMP)Wtsi/Y involves: C57BL/6 * C57BL/6N J:299010 View
Duane retraction syndrome Chn1tm1.1Ece/Chn1tm1.1Ece
Tg(Hlxb9-GFP)1Tmj/0		 involves: 129S1/Sv * 129S6/SvEvTac * C57BL/6J J:243785 View
Duane retraction syndrome Mafbtm1.2Good/Mafb+
Tg(Isl1-EGFP*)1Slp/0		 involves: 129S4/SvJae * BALB/c * C57BL/6 J:237642 View
Duane retraction syndrome Mafbtm1.2Good/Mafbtm1.2Good
Tg(Isl1-EGFP*)1Slp/0		 involves: 129S4/SvJae * BALB/c * C57BL/6 J:237642 View
Duchenne muscular dystrophy Barx2tm1Rsd/Barx2tm1Rsd
Dmdmdx/Dmdmdx		 involves: 129 * C57BL/6 * C57BL/10ScSn J:187799 View
Duchenne muscular dystrophy Barx2tm1Rsd/Barx2tm1Rsd
Dmdmdx/Y		 involves: 129 * C57BL/6 * C57BL/10ScSn J:187799 View
Duchenne muscular dystrophy Dmdem1Eno/Y involves: C57BL/6J J:253191 View
Duchenne muscular dystrophy Dmdem4Eno/Dmdem4Eno C57BL/6-Dmdem4Eno J:285447 View
Duchenne muscular dystrophy Dmdem4Eno/Y C57BL/6-Dmdem4Eno J:285447 View
Duchenne muscular dystrophy Dmdem#Tve/Y involves: C57BL/6 * CBA J:275476 View
Duchenne muscular dystrophy DmdGt(ROSABetageo)1Mpd/Y involves: 129S1/Sv J:47968 View
Duchenne muscular dystrophy Dmdmdx-3Cv/Y involves: C3H/HeHa * C57BL/6Ros * C57BL/10Sn * M. m. castaneus * M. m. musculus J:23375 View
Duchenne muscular dystrophy Dmdmdx-4Cv/Dmdmdx-4Cv
Terctm1Rdp/Terctm1Rdp		 B6.Cg-Terctm1Rdp Dmdmdx-4Cv J:200365 View
Duchenne muscular dystrophy Dmdmdx-5Cv/Dmdmdx-5Cv B6Ros.Cg-Dmdmdx-5Cv/J J:124861 View
Duchenne muscular dystrophy Dmdmdx-5Cv/Y B6Ros.Cg-Dmdmdx-5Cv J:177391 View
Duchenne muscular dystrophy Dmdmdx/?
Myod1tm1Jae/Myod1tm1Jae		 involves: 129S4/SvJae * C57BL/10ScSn J:52248 View
Duchenne muscular dystrophy Dmdmdx/Dmdmdx C57BL/10ScSn-Dmdmdx J:150127 View
Duchenne muscular dystrophy Dmdmdx/Dmdmdx C57BL/10ScSn-Dmdmdx/J J:7361 View
Duchenne muscular dystrophy Dmdmdx/Dmdmdx D2.B10-Dmdmdx J:160773 View
Duchenne muscular dystrophy Dmdmdx/Dmdmdx D2.B10-Dmdmdx/J J:226314 View
Duchenne muscular dystrophy Dmdmdx/Dmdmdx
Foxk1tm1Djg/Foxk1tm1Djg		 involves: 129S4/SvJae * C57BL/10ScSn J:62225 View
Duchenne muscular dystrophy Dmdmdx/Dmdmdx
Utrntm1Jrs/Utrntm1Jrs		 involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn J:42389, J:59675 View
Duchenne muscular dystrophy Dmdmdx/Dmdmdx
Utrntm1Ked/Utrntm1Ked		 involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * C57BL/10ScSn * DBA J:42388 View
Duchenne muscular dystrophy Dmdmdx/Y C57BL/10ScSn-Dmdmdx J:150127, J:177391 View
Duchenne muscular dystrophy Dmdmdx/Y C57BL/10ScSn-Dmdmdx/J J:7361 View
Duchenne muscular dystrophy Dmdmdx/Y
Dtnatm1Jrs/Dtnatm1Jrs		 involves: 129X1/SvJ * C57BL/10ScSn J:59675 View
Duchenne muscular dystrophy Dmdmdx/Y
Dtnatm1Jrs/Dtnatm1Jrs
Utrntm1Jrs/Utrntm1Jrs		 involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn J:59675 View
Duchenne muscular dystrophy Dmdmdx/Y
Foxk1tm1Djg/Foxk1tm1Djg		 involves: 129S4/SvJae * C57BL/10ScSn J:62225 View
Duchenne muscular dystrophy Dmdmdx/Y
Terctm1Rdp/Terctm1Rdp		 involves: 129/Sv * C57BL/6J * C57BL/10ScSn * SJL J:167294 View
Duchenne muscular dystrophy Dmdmdx/Y
Tg(DMD*)#Spc/0		 involves: 129P2/OlaHsd * C57BL/10ScSn * DBA/2 J:280218 View
Duchenne muscular dystrophy Dmdmdx/Y
Utrntm1Jrs/Utrn+		 involves: 129S1/Sv * 129X1/SvJ * C57BL/10ScSn J:140282 View
Duchenne muscular dystrophy Dmdtm1.1Khan/Y involves: C57BL/6 * CBA J:96210 View
Duchenne muscular dystrophy Dmdtm1Kmf/Y involves: C57BL/6 J:233298 View
Duchenne muscular dystrophy Dmdtm1Mok/Y involves: 129S/SvEv J:43164 View
Emery-Dreifuss muscular dystrophy Lmnatm1Gbon/Lmnatm1Gbon involves: 129S2/SvPas * C57BL/6 J:95528 View
Emery-Dreifuss muscular dystrophy Lmnatm1Stw/Lmnatm1Stw involves: 129S1/Sv J:58702 View
familial episodic pain syndrome 3 Scn11aem1Akoi/Scn11a+ involves: C57BL/6 J:268684 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
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
hereditary neuropathy with liability to pressure palsies Pmp22tm1Lnot/Pmp22+ Not Specified J:104989 View
hereditary neuropathy with liability to pressure palsies Pmp22tm1Ueli/Pmp22tm1Ueli involves: 129S/SvEv J:29517 View
hereditary neuropathy with liability to pressure palsies Pmp22Tr-2J/Pmp22+ C57BL/6J-Pmp22Tr-2J/GrsrJ J:201866 View
hereditary sensory and autonomic neuropathy type 6 Dstdt-23Rbrc/Dstdt-23Rbrc involves: C3H/HeN * C57BL/6 J:251779 View
hereditary sensory neuropathy Ntrk1tm1Bbd/Ntrk1tm1Bbd involves: 129S2/SvPas J:17194 View
hereditary sensory neuropathy Ntrk1tm1Par/Ntrk1tm1Par involves: 129S1/Sv * C57BL/6 J:60927 View
Leber hereditary optic neuropathy mt-Nd6m3Dwa B6.129S-mt-Nd6m3Dwa J:192260 View
megaconial type congenital muscular dystrophy Chkbrmd/Chkbrmd involves: BALB/cByJ * C57BL/6J J:108320 View
muscular dystrophy Fkrptvrm53/Fkrptvrm53 C57BL/6J-Fkrptvrm53/Pjn J:243745 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
myotonic dystrophy type 1 Dmpktm1Rdd/Dmpk+ involves: 129S2/SvPas * C57BL/6J J:53077 View
myotonic dystrophy type 1 Dmpktm1Rdd/Dmpktm1Rdd involves: 129S2/SvPas * C57BL/6J J:33714, J:53077 View
optic atrophy Opa1M1Bewi/Opa1+ involves: C3HeB/FeJ * C57BL/6 J:154966 View
optic atrophy Opa1Q285X/Opa1+ involves: C3HeB/FeJ * C57BL/6JCrl J:121779, J:189276 View
optic atrophy Opa1tm1.1Geno/Opa1+ involves: 129S2/SvPas J:237963 View
rigid spine muscular dystrophy 1 Selenontm1.2Mred/Selenontm1.2Mred involves: 129S2/SvPas * C57BL/6 * C57BL/6J * SJL J:176499 View
Riley-Day syndrome Elp1tm1.1Gilas/Elp1tm1.1Gilas
Tg(Dct-cre)1Apdn/0		 involves: 129S7/SvEvBrd * C57BL/6J J:237480 View
Riley-Day syndrome Elp1tm1.1Id/Elp1tm1.2Id involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA J:188923 View
Riley-Day syndrome Elp1tm1.1Id/Elp1tm1.2Id
Tg(IKBKAP*)#Sasl/0		 involves: 129S1/Sv * C57BL/6N J:229459 View
Riley-Day syndrome Elp1tm1.2Id/Elp1tm1.2Id involves: 129S1/Sv * C57BL/6 * C57BL/6J * CBA J:188923 View
Riley-Day syndrome Elp1tm1c(KOMP)Wtsi/Elp1tm1c(KOMP)Wtsi
H2az2Tg(Wnt1-cre)11Rth/H2az2+		 involves: C57BL/6J * C57BL/6N * CBA/J J:202989 View
tibial muscular dystrophy Ttntm1.1Isrd/Ttn+ involves: 129S2/SvPas * C57BL/6 J:165576 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
      Charcot-Marie-Tooth disease intermediate type Cfap276em2.1Fuxi/Cfap276+ involves: C57BL/6J J:295996 View
Charcot-Marie-Tooth disease intermediate type Cfap276em2.1Fuxi/Cfap276em2.1Fuxi involves: C57BL/6J J:295996 View
Charcot-Marie-Tooth disease type 6 Slc25a46atc/Slc25a46atc B6.Cg-Slc25a46atc J:242350 View
congenital fibrosis of the extraocular muscles Kif21atm1.1Ece/Kif21a+ involves: 129S1/Sv * 129S4/SvJae J:213171 View
congenital fibrosis of the extraocular muscles Kif21atm1.1Ece/Kif21atm1.1Ece involves: 129S1/Sv * 129S4/SvJae J:213171 View
congenital fibrosis of the extraocular muscles Kif21atm1.1Ece/Kif21atm1.1Ece
Tg(Isl1-EGFP*)1Slp/0		 involves: 129S1/Sv * 129S4/SvJae * BALB/c * C57BL/6 J:213171 View
congenital fibrosis of the extraocular muscles Tubb3tm1.1Ece/Tubb3tm1.1Ece involves: 129S/SvEv * C57BL/6J J:158992 View
congenital muscular dystrophy Col6a3tm1Chu/Col6a3tm1Chu B6.129-Col6a3tm1Chu J:198581 View
congenital nystagmus Ahrtm1Yfk/Ahrtm1Yfk involves: 129S/SvEv * C57BL/6J J:195817 View
distal myopathy Dnajb4em1Sngi/Dnajb4+ involves: C57BL/6J J:333950 View
distal myopathy Dnajb4em2Sngi/Dnajb4em2Sngi involves: C57BL/6J J:333950 View
distal myopathy Dysfim/Dysfim involves: SJL J:57764 View
distal myopathy Dysfprmd/Dysfprmd A/J J:92838 View
distal myopathy Dysftm1Kcam/Dysftm1Kcam involves: 129S1/Sv * 129X1/SvJ * C57BL/6 J:83126 View
distal myopathy Dysftm1Meho/Dysftm1Meho involves: 129S4/SvJae * C57BL/6 J:92838 View
Duchenne muscular dystrophy Tg(ACTA1-Ctss)1Jmol/? FVB/N-Tg(ACTA1-Ctss)1Jmol J:230788 View
Emery-Dreifuss muscular dystrophy Syne1tm1.1Mcn/Syne1tm1.1Mcn involves: 129S4/SvJae * 129S6/SvEvTac * C57BL J:144757 View
Emery-Dreifuss muscular dystrophy Zmpste24tm1Otin/Zmpste24tm1Otin involves: 129P2/Ola * C57BL/6 J:76209 View
facioscapulohumeral muscular dystrophy Fat1Gt(KST249)Byg/Fat1Gt(KST249)Byg
Tg(Myl1-lacZ)1Ibdml/0		 involves: 129P2/OlaHsd J:199157 View
facioscapulohumeral muscular dystrophy Fat1tm1.2Fhel/Fat1tm1.2Fhel
Tg(Myl1-lacZ)1Ibdml/0		 involves: 129S6/SvEvTac * BALB/cJ * C57BL/6J * SJL J:199157 View
facioscapulohumeral muscular dystrophy Fat1tm1Fhel/Fat1tm1Fhel
Pax3tm1(cre)Joe/Pax3+
Tg(Myl1-lacZ)1Ibdml/0		 involves: 129S6/SvEvTac * C57BL/6 * C57BL/6J * SJL J:199157 View
facioscapulohumeral muscular dystrophy Large1myd/Large1myd B6C3Fe a/a-Large1myd/J J:27793 View
hereditary sensory neuropathy DstTg4/DstTg4 involves: C57BL/6 * CD-1 J:209161 View
hereditary sensory neuropathy Scn11atm1.1Ikth/Scn11a+ involves: 129 * BALB/c * C57BL/6 J:206848 View
Lambert-Eaton myasthenic syndrome Cacna1atg-rol/Cacna1atg-rol involves: C57BL/6 * SIII J:164115 View
limb-girdle muscular dystrophy Tg(Ckm-Sgcg)4Mcn/0 involves: C57BL/6 * DBA/2 J:128649 View
motor peripheral neuropathy Chattm2(cre)Lowl/Chat+
Stmn2em2Jmi/Stmn2em2Jmi		 involves: 129S6/SvEvTac * C57BL/6J * C57BL/6N J:337175 View
motor peripheral neuropathy Slc12a6em1Dlp/Slc12a6em1Dlp involves: C57BL/6J J:259728 View
motor peripheral neuropathy Stmn2em1Jmi/Stmn2+ C57BL/6N-Stmn2em1Jmi J:337175 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
myotonic disease Mbnl1tm1Sws/Mbnl1tm1Sws involves: 129S1/Sv * C57BL/6J J:86903 View
myotonic disease Mbnl1tm1Sws/Mbnl1tm1Sws
Mbnl2tm1.1Sws/Mbnl2+		 involves: 129S1/Sv * 129S1/SvImJ * C57BL J:218011 View
neuromuscular disease Nemfem8Cx/Nemfem8Cx C57BL/6J-Nemfem8Cx/Cx J:296528 View
neuromuscular disease Nemfpdft/Nemfpdft B6(C3)-Nemfpdft/Cx J:296528 View
neuromuscular disease Nemftvrm116/Nemftvrm116 C57BL/6J-Nemftvrm116/PjnCx J:296528 View
neuropathy Mpztm1.1Wra/Mpz+ FVB.129S2-Mpztm1.1Wra J:267903 View
neuropathy Nemfem8Cx/Nemfem8Cx C57BL/6J-Nemfem8Cx/Cx J:296528 View
neuropathy Nemfpdft/Nemfpdft B6(C3)-Nemfpdft/Cx J:296528 View
neuropathy Nemftvrm116/Nemftvrm116 C57BL/6J-Nemftvrm116/PjnCx J:296528 View
neuropathy Stmn2em1Jmi/Stmn2em1Jmi C57BL/6N-Stmn2em1Jmi J:337175 View
neuropathy Tg(Mpz)80.2Wra/0 involves: FVB/N J:78758 View
optic atrophy Rpl24Bst/Rpl24+ involves: C57BLKS J:28035 View
scapuloperoneal myopathy Fhl1tm1.1Mihi/Y involves: 129S/SvEv * C57BL/6J * C57BL/6NJ J:218097 View
trigeminal neuralgia Gabrg1em1Ktka/Gabrg1em1Ktka involves: C57BL/6N J:299761 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
Walker-Warburg syndrome Col4a1deltaex40/Col4a1+ involves: 129S/SvEv * C57BL/6J J:172720 View
      Duchenne muscular dystrophy Itga7tm1Burk/Itga7tm1Burk
Sspntm1Kcam/Sspntm1Kcam		 involves: 129S1/Sv * 129X1/SvJ J:187752 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
oculopharyngeal muscular dystrophy Pabpn1tm1.2Gpvl/Pabpn1+ involves: C57BL/6 * FVB/N J:243638 View
Transgenes and
Other Mutations		     autosomal dominant limb-girdle muscular dystrophy type 1 Tg(Ckm-DNAJB6_ib*F93L)#Ccwe/0 B6.Cg-Tg(Ckm-DNAJB6_ib*F93L)#Ccwe J:226488 View
Charcot-Marie-Tooth disease axonal type 2F Tg(Thy1-HSPB1*S135F)#Lvdb/0 involves: FVB/N J:174508 View
Charcot-Marie-Tooth disease type 1A Tg(PMP22)C3Fbas/? B6.Cg-Tg(PMP22)C3Fbas J:237901 View
Charcot-Marie-Tooth disease type 1A Tg(PMP22)C22Clh/0 involves: C57BL/6J * CBA/Ca J:78221, J:76795 View
Charcot-Marie-Tooth disease type 1A Tg(PMP22)C61Clh/0 B6.Cg-Tg(PMP22)C61Clh J:158350 View
Charcot-Marie-Tooth disease type 1C Tg(CMV-LITAF*W116G)#Lli/Tg(CMV-LITAF*W116G)#Lli FVB-Tg(CMV-LITAF*W116G)#Lli J:194981 View
Charcot-Marie-Tooth disease type 2A2A Tg(Eno2-MFN2*R94Q)L51Ugfm/0 involves: C57BL/6 * C57BL/6J * DBA/2 J:158936 View
Charcot-Marie-Tooth disease type 2A2A Tg(Eno2-MFN2*R94Q)L51Ugfm/0 involves: C57BL/6 * DBA/2 J:173431 View
Charcot-Marie-Tooth disease type 2A2A Tg(Eno2-MFN2*R94Q)L87Ugfm/Tg(Eno2-MFN2*R94Q)L87Ugfm involves: C57BL/6 * DBA/2 J:173431 View
Charcot-Marie-Tooth disease type 2E Tg(NEFL*E397K)#Milg/0 Not Specified J:173771 View
Charcot-Marie-Tooth disease type 2E Tg(tetO-NEFL)173.2Jpj/0
Tg(THY1-tTA)177Jpj/0		 involves: C3H * C57BL/6 J:160704 View
facioscapulohumeral muscular dystrophy Tg(ACTA1-FRG1)highRotu/0 C57BL/6-Tg(ACTA1-FRG1)highRotu J:106896 View
facioscapulohumeral muscular dystrophy Tg(ACTA1-FRG1)medRotu/0 C57BL/6-Tg(ACTA1-FRG1)medRotu J:106896 View
hereditary sensory neuropathy Tg(CAG-SPTLC1*C133W)8EAmcc/0 involves: C3H * C57BL/6 J:106812 View
Leber hereditary optic neuropathy Tg(LONP1-mt-ND4*,-mCherry*)#Jguy B6(D2)-Tg(LONP1-mt-ND4*,-mCherry*)#Jguy J:224897 View
myotonic dystrophy type 1 A1cfTg(Myh6-cre/Esr1*)1Jmk/A1cf+
Tg(CAG-DMPK*)1323Coop/0		 involves: FVB J:127391 View
myotonic dystrophy type 1 Tg(ACTA1-cre/ERT2)97.16Mtz/0
Tg(CAG-DMPK*)1323Coop/0		 involves: FVB J:132154 View
myotonic dystrophy type 1 Tg(Ckm-CUGBP1)1039Coop/0 FVB-Tg(Ckm-CUGBP1)1039Coop J:99370 View
myotonic dystrophy type 1 Tg(DM15)26Bew/0 involves: FVB J:93614 View
myotonic dystrophy type 1 Tg(DMPK/tetO-EGFP/DMPK)5-313Masm/0 involves: FVB/N J:207560 View
myotonic dystrophy type 1 Tg(DMWD,DMPK*,SIX5)328Ggo/Tg(DMWD,DMPK*,SIX5)328Ggo involves: C57BL/6 * DBA/2 J:73187, J:196337 View
myotonic dystrophy type 1 Tg(DMWD,DMPK*,SIX5)1177Ggo/Tg(DMWD,DMPK*,SIX5)1177Ggo involves: C57BL/6 * DBA/2 J:73187 View
myotonic dystrophy type 1 Tg(HSA*LR)20aCath/? involves: FVB/N J:64493 View
myotonic dystrophy type 1 Tg(HSA*LR)20bCath/? involves: FVB/N J:64493 View
myotonic dystrophy type 1 Tg(HSA*LR)21Cath/? involves: FVB/N J:64493 View
myotonic dystrophy type 1 Tg(HSA*LR)32aCath/? involves: FVB/N J:64493 View
myotonic dystrophy type 1 Tg(HSA*LR)32bCath/? involves: FVB/N J:64493 View
myotonic dystrophy type 1 Tg(HSA*LR)41Cath/? involves: FVB/N J:64493 View
myotonic dystrophy type 1 Tg(Myh6-rtTA)8585Jam/0
Tg(tetO-CUGBP1)3413Coop/0		 involves: FVB * FVB/N * FVB/NTac J:157646 View
oculopharyngeal muscular dystrophy Tg(ACTA1-PABPN1*A17)1Drub/0 involves: FVB/N J:115642 View
Additional
Complex
Models		     Charcot-Marie-Tooth disease type 2A2A Gt(ROSA)26Sortm1(CAG-MFN2*T105M)Dple/Gt(ROSA)26Sor+
Tg(Nes-cre)1Kln/0		 involves: C57BL/6 * SJL J:251584 View
facioscapulohumeral muscular dystrophy Gt(ROSA)26Sortm1(DUX4)Sqh/Gt(ROSA)26Sor+
Tg(ACTA1-cre/Esr1*)2Kesr/0		 involves: 129S6/SvEvTac * C3H * C57BL/6 J:268959 View
facioscapulohumeral muscular dystrophy Gt(ROSA)26Sortm1.1(DUX4*)Plj/Gt(ROSA)26Sor+
Tg(ACTA1-cre/Esr1*)2Kesr/0		 involves: C3H * C57BL/6 J:256652 View
oculopharyngeal muscular dystrophy Tg(CAG-GLVP)#Cath/0
Tg(GAL4-PABPN1*A16)#Cath/0		 involves: C57BL/6 * FVB J:178541 View
optic atrophy Fdxrm1J/Fdxrm1J
Otop2m1J/Otop2m1J		 B6;129S-Fdxrm1J Otop2m1J/GrsrJ J:247931 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
Charcot-Marie-Tooth disease type 2B1 Lmnatm1.1Vde/Lmnatm1.1Vde B6.129(Cg)-Lmnatm1.1Vde J:322912 View
tibial muscular dystrophy Capn3tm1Jsb/Capn3+
Ttntm1.1Isrd/Ttn+		 involves: 129/Sv * 129S2/SvPas * C57BL/6 J:165576 View