| Disease Term | Human Homologs | Mouse Homologs | Mouse Models | Homology Source | |||
  | cerebellar ataxia type 42 | CACNA1G* | Cacna1g* | 2 models | Alliance of Genome Resources | ||
| spinocerebellar ataxia type 1 | ATXN1* | Atxn1* | 1 model | Alliance of Genome Resources | |||
| spinocerebellar ataxia type 14 | PRKCG* | Prkcg* | 2 models | Alliance of Genome Resources | |||
| spinocerebellar ataxia type 17 | TBP* | Tbp* | 1 model | Alliance of Genome Resources | |||
| spinocerebellar ataxia type 2 | ATXN2* | Atxn2* | 1 model | Alliance of Genome Resources | |||
| spinocerebellar ataxia type 28 | AFG3L2* | Afg3l2* | 1 model | Alliance of Genome Resources | |||
| spinocerebellar ataxia type 5 | SPTBN2* | Sptbn2* | 2 models | Alliance of Genome Resources | |||
| spinocerebellar ataxia type 6 | CACNA1A* | Cacna1a* | 3 models | Alliance of Genome Resources | |||
| spinocerebellar ataxia type 7 | ATXN7* | Atxn7* | 5 models | Alliance of Genome Resources | |||
| | spinocerebellar ataxia type 27 | FGF14 | Fgf14* | 1 model | Alliance of Genome Resources | ||
| | autosomal dominant cerebellar ataxia | SAMD9L* | Samd9l | Alliance of Genome Resources | |||
| autosomal dominant cerebellar ataxia | NPTX1* | Nptx1 | Alliance of Genome Resources | ||||
| autosomal dominant cerebellar ataxia | FGF14* | Fgf14 | Alliance of Genome Resources | ||||
| autosomal dominant cerebellar ataxia, deafness and narcolepsy | DNMT1* | Dnmt1 | Alliance of Genome Resources | ||||
| cerebellar ataxia type 41 | TRPC3* | Trpc3 | Alliance of Genome Resources | ||||
| cerebellar ataxia type 43 | MME* | Mme | Alliance of Genome Resources | ||||
| cerebellar ataxia type 47 | PUM1* | Pum1 | Alliance of Genome Resources | ||||
| cerebellar ataxia type 48 | STUB1* | Stub1 | Alliance of Genome Resources | ||||
| dentatorubral-pallidoluysian atrophy | ATN1* | Atn1 | Alliance of Genome Resources | ||||
| Machado-Joseph disease | BECN1* | Becn1 | Alliance of Genome Resources | ||||
| Machado-Joseph disease | ATXN3* | Atxn3 | 1 model | Alliance of Genome Resources | |||
| nonprogressive cerebellar ataxia with mental retardation | CAMTA1* | Camta1 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia 44 | GRM1* | Grm1 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia 45 | FAT2* | Fat2 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia 46 | PLD3* | Pld3 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 10 | ATXN10* | Atxn10 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 11 | TTBK2* | Ttbk2 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 12 | PPP2R2B* | Ppp2r2b | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 13 | KCNC3* | Kcnc3 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 15 | ITPR1* | Itpr1 | 2 models | Alliance of Genome Resources | |||
| spinocerebellar ataxia type 19/22 | KCND3* | Kcnd3 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 21 | TMEM240* | Tmem240 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 23 | PDYN* | Pdyn | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 25 | PNPT1* | Pnpt1 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 26 | EEF2* | Eef2 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 29 | ITPR1* | Itpr1 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 31 | BEAN1* | Bean1 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 34 | ELOVL4* | Elovl4 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 35 | TGM6* | Tgm6 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 36 | NOP56* | Nop56 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 37 | DAB1* | Dab1 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 38 | ELOVL5* | Elovl5 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 4 | ZFHX3* | Zfhx3 | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 40 | CCDC88C* | Ccdc88c | Alliance of Genome Resources | ||||
| spinocerebellar ataxia type 8 | ATXN8* | ||||||
| spinocerebellar ataxia type 8 | ATXN8OS* | ||||||
Excel File
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Transgenes and other genome features developed in mice to model this disease.
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| Disease Term | Transgenes and Other Genome Features | Mouse Models | |
| dentatorubral-pallidoluysian atrophy | Tg(Prnp-ATN1)124Dbo | 1 model | |
| dentatorubral-pallidoluysian atrophy | Tg(Eno2-ATN1)14Tx | 1 model | |
| dentatorubral-pallidoluysian atrophy | Tg(Eno2-ATN1)3Tx | 1 model | |
| dentatorubral-pallidoluysian atrophy | Tg(ATN1*)Q129Stsu | 1 model | |
| dentatorubral-pallidoluysian atrophy | Tg(Prnp-ATN1)150Dbo | 1 model | |
| Machado-Joseph disease | Tg(Pcp2-ATXN3*69Q)bHirai | 1 model | |
| Machado-Joseph disease | Tg(Prnp-ATXN3*79Q)#Hlw | 1 model | |
| Machado-Joseph disease | Tg(ATXN3*)67.2Cce | 2 models | |
| Machado-Joseph disease | Tg(ATXN3*)84.2Cce | 3 models | |
| Machado-Joseph disease | Tg(CMV-ATXN3*94Q)94Pama | 2 models | |
| Machado-Joseph disease | Tg(CMV-ATXN3*135Q)CPama | 1 model | |
| Machado-Joseph disease | Tg(Htt-ATXN3*148Q)3746Thsc | 1 model | |
| Machado-Joseph disease | Tg(Prnp-ATXN3*70Q)70.61Olri | 1 model | |
| Machado-Joseph disease | Tg(Prnp-ATXN3*148Q)NLS.28Olri | 1 model | |
| Machado-Joseph disease | Tg(Prnp-ATXN3*148Q)148.19Olri | 1 model | |
| spinocerebellar ataxia type 1 | Tg(Pcp2-ATXN1*82Q)5Horr | 1 model | |
| spinocerebellar ataxia type 1 | Tg(tetO-ATXN1*82Q)#Horr | 1 model | |
| spinocerebellar ataxia type 10 | Tg(Prnp-lacZ/ATXN10*)#Teas | 1 model | |
| spinocerebellar ataxia type 14 | Tg(tetO-PRKCG*S361G,-GFP)3Jpka | 1 model | |
| spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)71-27Xjl | 1 model | |
| spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)71-16Xjl | 1 model | |
| spinocerebellar ataxia type 17 | Tg(Pcp2-TBP*)69Hmhl | 1 model | |
| spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)105Xjl | 1 model | |
| spinocerebellar ataxia type 2 | Tg(Pcp2-ATXN2*127Q)#Plt | 1 model | |
| spinocerebellar ataxia type 2 | Tg(ATXN2*72Q)#Plt | 1 model | |
| spinocerebellar ataxia type 5 | Tg(tetO-SPTBN2*)#Lpwr | 1 model | |
| spinocerebellar ataxia type 7 | Tg(Prnp-ATXN7*92Q)6076Als | 1 model | |
| spinocerebellar ataxia type 7 | Tg(GFAP-ATXN7*92Q)2542Als | 1 model | |
| spinocerebellar ataxia type 7 | Tg(GFAP-ATXN7*92Q)2521Als | 1 model | |
| spinocerebellar ataxia type 7 | Tg(Prnp-ATXN7*92Q)1963Als | 1 model | |
| spinocerebellar ataxia type 7 | Tg(Pcp2-SCA7)P7EJman | 1 model | |
| spinocerebellar ataxia type 7 | Tg(RHO-SCA7)R7EJman | 1 model | |