Excel File Text File *Disease is associated/modeled with this Gene or a homolog. More...
      Disease Term Human Homologs Mouse Homologs Mouse Models Homology Source
     ataxia telangiectasia ATM* Atm* 9 models Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 12 WWOX* Wwox* 1 model Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 13 GRM1* Grm1* 1 model Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 16 STUB1* Stub1* 1 model Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 18 GRID2* Grid2* 2 models Alliance of Genome Resources
Cayman type cerebellar ataxia ATCAY* Atcay* 3 models Alliance of Genome Resources
cerebellar ataxia type 42 CACNA1G* Cacna1g* 2 models Alliance of Genome Resources
Charlevoix-Saguenay spastic ataxia SACS* Sacs* 2 models Alliance of Genome Resources
Friedreich ataxia FXN* Fxn* 8 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 with axonal neuropathy 1 TDP1* Tdp1* 1 model Alliance of Genome Resources
     cerebellar ataxia CACNA1A Cacna1a* 1 model Alliance of Genome Resources
Charlevoix-Saguenay spastic ataxia ANKFY1 Ankfy1* 1 model Alliance of Genome Resources
spinocerebellar ataxia type 27 FGF14 Fgf14* 1 model Alliance of Genome Resources
     ataxia-oculomotor apraxia type 4 PNKP* Pnkp   Alliance of Genome Resources
ataxia telangiectasia BAK1* Bak1   Alliance of Genome Resources
ataxia telangiectasia BAX* Bax   Alliance of Genome Resources
ataxia telangiectasia IL2* Il2   Alliance of Genome Resources
ataxia telangiectasia IFNG* Ifng   Alliance of Genome Resources
ataxia telangiectasia HDAC4* Hdac4   Alliance of Genome Resources
ataxia telangiectasia BIK* Bik   Alliance of Genome Resources
ataxia-telangiectasia-like disorder-1 MRE11* Mre11a   Alliance of Genome Resources
ataxia-telangiectasia-like disorder-2 PCNA* Pcna   Alliance of Genome Resources
ataxia with oculomotor apraxia type 1 APTX* Aptx   Alliance of Genome Resources
ataxia with oculomotor apraxia type 3 PIK3R5* Pik3r5   Alliance of Genome Resources
autosomal dominant cerebellar ataxia SAMD9L* Samd9l   Alliance of Genome Resources
autosomal dominant cerebellar ataxia FGF14* Fgf14   Alliance of Genome Resources
autosomal dominant cerebellar ataxia NPTX1* Nptx1   Alliance of Genome Resources
autosomal dominant cerebellar ataxia, deafness and narcolepsy DNMT1* Dnmt1   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 10 ANO10* Ano10   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 11 SYT14* Syt14   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 14 SPTBN2* Sptbn2   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 15 RUBCN* Rubcn   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 17 CWF19L1* Cwf19l1   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 19 SLC9A1* Slc9a1   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 2 PMPCA* Pmpca   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 20 SNX14* Snx14   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 21 SCYL1* Scyl1   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 22 VWA3B* Vwa3b   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 23 TDP2* Tdp2   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 24 UBA5* Uba5   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 25 ATG5* Atg5   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 26 XRCC1* Xrcc1   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 27 GDAP2* Gdap2   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 28 THG1L* Thg1l   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 29 VPS41* Vps41   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 30 PITRM1* Pitrm1   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 31 ATG7* Atg7   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 32 PRDX3* Prdx3   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 33 RNU12*  
autosomal recessive spinocerebellar ataxia 4 VPS13D* Vps13d   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 7 TPP1* Tpp1   Alliance of Genome Resources
autosomal recessive spinocerebellar ataxia 8 SYNE1* Syne1   Alliance of Genome Resources
cerebellar ataxia RPGRIP1L* Rpgrip1l   Alliance of Genome Resources
cerebellar ataxia SYNE1* Syne1   Alliance of Genome Resources
cerebellar ataxia POLG* Polg   Alliance of Genome Resources
cerebellar ataxia L2HGDH* L2hgdh   Alliance of Genome Resources
cerebellar ataxia ATCAY* Atcay   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
Friedreich ataxia AGTR1* Agtr1a, Agtr1b   Alliance of Genome Resources
Friedreich ataxia ND1* mt-Nd1   Alliance of Genome Resources
Friedreich ataxia 1 FXN* Fxn   Alliance of Genome Resources
Machado-Joseph disease ATXN3* Atxn3 1 model Alliance of Genome Resources
Machado-Joseph disease BECN1* Becn1   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*  
spinocerebellar ataxia with axonal neuropathy 2 SETX* Setx   Alliance of Genome Resources
spinocerebellar ataxia with axonal neuropathy type 3 COA7* Coa7   Alliance of Genome Resources

 
Transgenes and other genome features developed in mice to model this disease.
     Disease Term Transgenes and Other Genome Features Mouse Models
  dentatorubral-pallidoluysian atrophy Tg(Eno2-ATN1)14Tx 1 model
  dentatorubral-pallidoluysian atrophy Tg(Eno2-ATN1)3Tx 1 model
  dentatorubral-pallidoluysian atrophy Tg(Prnp-ATN1)124Dbo 1 model
  dentatorubral-pallidoluysian atrophy Tg(Prnp-ATN1)150Dbo 1 model
  dentatorubral-pallidoluysian atrophy Tg(ATN1*)Q129Stsu 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(Pcp2-ATXN3*69Q)bHirai 1 model
  Machado-Joseph disease Tg(Prnp-ATXN3*70Q)70.61Olri 1 model
  Machado-Joseph disease Tg(Prnp-ATXN3*79Q)#Hlw 1 model
  Machado-Joseph disease Tg(Prnp-ATXN3*148Q)148.19Olri 1 model
  Machado-Joseph disease Tg(Prnp-ATXN3*148Q)NLS.28Olri 1 model
  spinocerebellar ataxia type 1 Tg(tetO-ATXN1*82Q)#Horr 1 model
  spinocerebellar ataxia type 1 Tg(Pcp2-ATXN1*82Q)5Horr 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*)105Xjl 1 model
  spinocerebellar ataxia type 17 Tg(Pcp2-TBP*)69Hmhl 1 model
  spinocerebellar ataxia type 17 Tg(Prnp-TBP*)71-16Xjl 1 model
  spinocerebellar ataxia type 2 Tg(ATXN2*72Q)#Plt 1 model
  spinocerebellar ataxia type 2 Tg(Pcp2-ATXN2*127Q)#Plt 1 model
  spinocerebellar ataxia type 5 Tg(tetO-SPTBN2*)#Lpwr 1 model
  spinocerebellar ataxia type 7 Tg(RHO-SCA7)R7EJman 1 model
  spinocerebellar ataxia type 7 Tg(Prnp-ATXN7*92Q)6076Als 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(GFAP-ATXN7*92Q)2542Als 1 model
  spinocerebellar ataxia type 7 Tg(GFAP-ATXN7*92Q)2521Als 1 model