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
     adrenoleukodystrophy ABCD1* Abcd1* 9 models Alliance of Genome Resources
adult-onset autosomal dominant demyelinating leukodystrophy LMNB1* Lmnb1* 3 models Alliance of Genome Resources
Alexander disease GFAP* Gfap* 7 models Alliance of Genome Resources
ataxia telangiectasia ATM* Atm* 9 models Alliance of Genome Resources
Athabaskan brainstem dysgenesis syndrome HOXA1* Hoxa1* 1 model Alliance of Genome Resources
atypical teratoid rhabdoid tumor SMARCB1* Smarcb1* 3 models Alliance of Genome Resources
autosomal dominant nocturnal frontal lobe epilepsy 3 CHRNB2* Chrnb2* 2 models 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
basal ganglia calcification SLC20A2* Slc20a2* 1 model Alliance of Genome Resources
basal ganglia calcification PDGFRB* Pdgfrb* 1 model Alliance of Genome Resources
benign neonatal seizures KCNQ2* Kcnq2* 5 models Alliance of Genome Resources
benign neonatal seizures KCNQ3* Kcnq3* 5 models Alliance of Genome Resources
biotin-responsive basal ganglia disease SLC19A3* Slc19a3* 2 models Alliance of Genome Resources
brain small vessel disease 1 COL4A1* Col4a1* 1 model Alliance of Genome Resources
CADASIL 1 NOTCH3* Notch3* 8 models Alliance of Genome Resources
Canavan disease ASPA* Aspa* 4 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
cerebral cavernous malformation 2 CCM2* Ccm2* 4 models Alliance of Genome Resources
cerebral cavernous malformation 3 PDCD10* Pdcd10* 2 models Alliance of Genome Resources
Charlevoix-Saguenay spastic ataxia SACS* Sacs* 2 models Alliance of Genome Resources
complex cortical dysplasia with other brain malformations 7 TUBB2B* Tubb2b* 1 model Alliance of Genome Resources
cortical dysplasia-focal epilepsy syndrome CNTNAP2* Cntnap2* 1 model Alliance of Genome Resources
Creutzfeldt-Jakob disease PRNP* Prnp* 8 models Alliance of Genome Resources
developmental and epileptic encephalopathy 16 TBC1D24* Tbc1d24* 1 model Alliance of Genome Resources
developmental and epileptic encephalopathy 17 GNAO1* Gnao1* 3 models Alliance of Genome Resources
developmental and epileptic encephalopathy 2 CDKL5* Cdkl5* 2 models Alliance of Genome Resources
developmental and epileptic encephalopathy 39 SLC25A12* Slc25a12* 1 model Alliance of Genome Resources
developmental and epileptic encephalopathy 7 KCNQ2* Kcnq2* 1 model Alliance of Genome Resources
Dravet syndrome SCN1A* Scn1a* 8 models Alliance of Genome Resources
episodic kinesigenic dyskinesia 1 PRRT2* Prrt2* 2 models Alliance of Genome Resources
familial hemiplegic migraine 2 ATP1A2* Atp1a2* 2 models Alliance of Genome Resources
familial temporal lobe epilepsy 1 LGI1* Lgi1* 4 models Alliance of Genome Resources
fatal familial insomnia PRNP* Prnp* 1 model Alliance of Genome Resources
Gerstmann-Straussler-Scheinker syndrome PRNP* Prnp* 7 models Alliance of Genome Resources
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions GRN* Grn* 3 models Alliance of Genome Resources
hypomyelinating leukodystrophy 2 GJC2* Gjc2* 3 models Alliance of Genome Resources
hypomyelinating leukodystrophy 6 TUBB4A* Tubb4a* 3 models Alliance of Genome Resources
Joubert syndrome 17 CPLANE1* Cplane1* 1 model Alliance of Genome Resources
Joubert syndrome 26 KATNIP* Katnip* 1 model Alliance of Genome Resources
Joubert syndrome 3 AHI1* Ahi1* 1 model Alliance of Genome Resources
Joubert syndrome 5 CEP290* Cep290* 2 models Alliance of Genome Resources
Joubert syndrome 6 TMEM67* Tmem67* 1 model Alliance of Genome Resources
Joubert syndrome 7 RPGRIP1L* Rpgrip1l* 1 model Alliance of Genome Resources
juvenile myoclonic epilepsy EFHC1* Efhc1* 2 models Alliance of Genome Resources
L-2-hydroxyglutaric aciduria L2HGDH* L2hgdh* 1 model Alliance of Genome Resources
Lafora disease EPM2A* Epm2a* 2 models Alliance of Genome Resources
Lafora disease NHLRC1* Nhlrc1* 3 models Alliance of Genome Resources
leukoencephalopathy with vanishing white matter EIF2B5* Eif2b5* 7 models Alliance of Genome Resources
leukoencephalopathy with vanishing white matter EIF2B4* Eif2b4* 4 models Alliance of Genome Resources
megalencephalic leukoencephalopathy with subcortical cysts 1 MLC1* Mlc1* 1 model Alliance of Genome Resources
myoclonic dystonia 11 SGCE* Sgce* 2 models Alliance of Genome Resources
neurodevelopmental disorder with involuntary movements GNAO1* Gnao1* 1 model Alliance of Genome Resources
normal pressure hydrocephalus CFAP43* Cfap43* 1 model Alliance of Genome Resources
paroxysmal nonkinesigenic dyskinesia 1 PNKD* Pnkd* 2 models Alliance of Genome Resources
Pelizaeus-Merzbacher disease PLP1* Plp1* 7 models Alliance of Genome Resources
progressive myoclonus epilepsy 1B PRICKLE1* Prickle1* 1 model Alliance of Genome Resources
pyridoxine-dependent epilepsy ALDH7A1* Aldh7a1* 1 model Alliance of Genome Resources
spinocerebellar ataxia type 14 PRKCG* Prkcg* 3 models Alliance of Genome Resources
spinocerebellar ataxia type 17 TBP* Tbp* 5 models Alliance of Genome Resources
spinocerebellar ataxia type 2 ATXN2* Atxn2* 2 models Alliance of Genome Resources
spinocerebellar ataxia type 27 FGF14* Fgf14* 1 model Alliance of Genome Resources
spinocerebellar ataxia type 28 AFG3L2* Afg3l2* 1 model Alliance of Genome Resources
spinocerebellar ataxia type 5 SPTBN2* Sptbn2* 3 models Alliance of Genome Resources
spinocerebellar ataxia type 6 CACNA1A* Cacna1a* 3 models Alliance of Genome Resources
spinocerebellar ataxia type 7 ATXN7* Atxn7* 11 models Alliance of Genome Resources
torsion dystonia 1 TOR1A* Tor1a* 7 models Alliance of Genome Resources
torsion dystonia 6 THAP1* Thap1* 2 models Alliance of Genome Resources
     arteriovenous malformations of the brain ENG Eng* 1 model Alliance of Genome Resources
arteriovenous malformations of the brain ACVRL1 Acvrl1* 1 model Alliance of Genome Resources
arteriovenous malformations of the brain NOTCH4 Notch4* 1 model Alliance of Genome Resources
brain disease PTEN Pten* 1 model Alliance of Genome Resources
Canavan disease SOD2 Sod2* 1 model Alliance of Genome Resources
cerebellar ataxia CACNA1A Cacna1a* 1 model Alliance of Genome Resources
cerebellar disease ZNF423 Zfp423* 1 model Alliance of Genome Resources
cerebral cavernous malformation KRIT1 Krit1* 1 model Alliance of Genome Resources
Charlevoix-Saguenay spastic ataxia ANKFY1 Ankfy1* 1 model Alliance of Genome Resources
childhood electroclinical syndrome CACNA1A Cacna1a* 1 model Alliance of Genome Resources
Dandy-Walker syndrome ZIC1 Zic1* 1 model Alliance of Genome Resources
Dandy-Walker syndrome ZIC4 Zic4* 1 model Alliance of Genome Resources
Dandy-Walker syndrome ZNF423 Zfp423* 1 model Alliance of Genome Resources
early infantile epileptic encephalopathy ARX Arx* 7 models Alliance of Genome Resources
early infantile epileptic encephalopathy SCN8A Scn8a* 1 model Alliance of Genome Resources
epilepsy ALDH5A1 Aldh5a1* 1 model Alliance of Genome Resources
epilepsy BSN Bsn* 1 model Alliance of Genome Resources
epilepsy C1QA C1qa* 1 model Alliance of Genome Resources
epilepsy CACNA2D2 Cacna2d2* 1 model Alliance of Genome Resources
epilepsy CDYL Cdyl* 1 model Alliance of Genome Resources
epilepsy GAD2 Gad2* 1 model Alliance of Genome Resources
epilepsy KCNA1 Kcna1* 1 model Alliance of Genome Resources
epilepsy SCAMP5 Scamp5* 1 model Alliance of Genome Resources
epilepsy SCN8A Scn8a* 1 model Alliance of Genome Resources
epilepsy SLC12A5 Slc12a5* 1 model Alliance of Genome Resources
epilepsy SYN2 Syn2* 2 models Alliance of Genome Resources
familial hemiplegic migraine CACNA1A Cacna1a* 5 models Alliance of Genome Resources
focal dystonia TOR1A Tor1a* 1 model Alliance of Genome Resources
Friedreich ataxia FXN Fxn* 6 models Alliance of Genome Resources
frontotemporal dementia TREM2 Trem2* 1 model Alliance of Genome Resources
frontotemporal dementia VCP Vcp* 1 model Alliance of Genome Resources
frontotemporal dementia TARDBP Tardbp* 6 models Alliance of Genome Resources
frontotemporal dementia CHMP2B Chmp2b* 4 models Alliance of Genome Resources
generalized dystonia CACNA1A Cacna1a* 2 models Alliance of Genome Resources
generalized epilepsy with febrile seizures plus SCN1A Scn1a* 5 models Alliance of Genome Resources
generalized epilepsy with febrile seizures plus SCN1B Scn1b* 1 model Alliance of Genome Resources
generalized epilepsy with febrile seizures plus GABRG2 Gabrg2* 1 model Alliance of Genome Resources
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions TARDBP Tardbp* 7 models Alliance of Genome Resources
hydrocephalus ADD1 Add1* 1 model Alliance of Genome Resources
hydrocephalus AK8 Ak8* 1 model Alliance of Genome Resources
hydrocephalus E2F5 E2f5* 1 model Alliance of Genome Resources
hydrocephalus AK7 Ak7* 1 model Alliance of Genome Resources
hydrocephalus DPCD Dpcd* 1 model Alliance of Genome Resources
hydrocephalus CELSR2 Celsr2* 1 model Alliance of Genome Resources
hydrocephalus CCDC85C Ccdc85c* 1 model Alliance of Genome Resources
hydrocephalus CCDC39 Ccdc39* 1 model Alliance of Genome Resources
hydrocephalus ULK4 Ulk4* 1 model Alliance of Genome Resources
hydrocephalus STK36 Stk36* 1 model Alliance of Genome Resources
hydrocephalus SOX3 Sox3* 1 model Alliance of Genome Resources
hydrocephalus POMK Pomk* 1 model Alliance of Genome Resources
hydrocephalus NME7 Nme7* 1 model Alliance of Genome Resources
hydrocephalus NME5 Nme5* 1 model Alliance of Genome Resources
hydrocephalus MBOAT7 Mboat7* 1 model Alliance of Genome Resources
hydrocephalus KIF27 Kif27* 1 model Alliance of Genome Resources
hydrocephalus HYDIN Hydin* 1 model Alliance of Genome Resources
idiopathic generalized epilepsy DNM1 Dnm1* 2 models Alliance of Genome Resources
idiopathic generalized epilepsy GABRA1 Gabra1* 3 models Alliance of Genome Resources
Joubert syndrome ZIC1 Zic1* 1 model Alliance of Genome Resources
Lennox-Gastaut syndrome DGKD Dgkd* 1 model Alliance of Genome Resources
leukodystrophy CLCN2 Clcn2* 1 model Alliance of Genome Resources
medulloblastoma SMO Smo* 8 models Alliance of Genome Resources
medulloblastoma PTCH1 Ptch1* 12 models Alliance of Genome Resources
medulloblastoma IFNG Ifng* 2 models Alliance of Genome Resources
megalencephalic leukoencephalopathy with subcortical cysts HEPACAM Hepacam* 1 model Alliance of Genome Resources
movement disease EFNB3 Efnb3* 1 model Alliance of Genome Resources
neuroaxonal dystrophy BORCS7 Borcs7* 1 model Alliance of Genome Resources
normal pressure hydrocephalus p23-ST1* 1 model
obstructive hydrocephalus MYO9A Myo9a* 1 model Alliance of Genome Resources
porencephaly COL4A1 Col4a1* 1 model Alliance of Genome Resources
progressive myoclonus epilepsy SCARB2 Scarb2* 1 model Alliance of Genome Resources
Stiff-Person syndrome TRAK1 Trak1* 1 model Alliance of Genome Resources
temporal lobe epilepsy GLUL Glul* 1 model Alliance of Genome Resources
temporal lobe epilepsy SLC32A1 Slc32a1* 1 model Alliance of Genome Resources
temporal lobe epilepsy KCNA1 Kcna1* 1 model Alliance of Genome Resources
Unverricht-Lundborg syndrome CSTB Cstb* 1 model Alliance of Genome Resources
     adult-onset leukoencephalopathy with axonal spheroids and pigmented glia CSF1R* Csf1r   Alliance of Genome Resources
arteriovenous malformations of the brain KRAS* Kras   Alliance of Genome Resources
arteriovenous malformations of the brain IL6* Il6   Alliance of Genome Resources
ataxia with oculomotor apraxia type 1 APTX* Aptx   Alliance of Genome Resources
ataxia with oculomotor apraxia type 2 SETX* Setx   Alliance of Genome Resources
ataxia with oculomotor apraxia type 3 PIK3R5* Pik3r5   Alliance of Genome Resources
autosomal dominant cerebellar ataxia, deafness and narcolepsy DNMT1* Dnmt1   Alliance of Genome Resources
autosomal dominant nocturnal frontal lobe epilepsy 1 CHRNA4* Chrna4 1 "NOT" model Alliance of Genome Resources
autosomal dominant nocturnal frontal lobe epilepsy 4 CHRNA2* Chrna2   Alliance of Genome Resources
autosomal dominant nocturnal frontal lobe epilepsy 5 KCNT1* Kcnt1   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 12 WWOX* Wwox   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 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
basal ganglia calcification PDGFB* Pdgfb   Alliance of Genome Resources
benign familial infantile epilepsy SCN2A* Scn2a   Alliance of Genome Resources
benign familial infantile epilepsy PRRT2* Prrt2   Alliance of Genome Resources
bilateral frontoparietal polymicrogyria ADGRG1* Adgrg1   Alliance of Genome Resources
bilateral parasagittal parieto-occipital polymicrogyria FIG4* Fig4   Alliance of Genome Resources
bilateral perisylvian polymicrogyria ADGRG1* Adgrg1   Alliance of Genome Resources
brain small vessel disease 2 COL4A2* Col4a2   Alliance of Genome Resources
brain small vessel disease 3 COLGALT1* Colgalt1   Alliance of Genome Resources
CADASIL HTRA1* Htra1   Alliance of Genome Resources
CADASIL 2 HTRA1* Htra1   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
cerebral cavernous malformation 1 KRIT1* Krit1   Alliance of Genome Resources
cerebral infarction F2* F2   Alliance of Genome Resources
cerebral infarction PRKCH* Prkch   Alliance of Genome Resources
cerebral infarction NOS3* Nos3   Alliance of Genome Resources
cerebral infarction F5* F5   Alliance of Genome Resources
cerebral infarction ALOX5AP* Alox5ap   Alliance of Genome Resources
childhood onset epileptic encephalopathy CHD2* Chd2   Alliance of Genome Resources
childhood onset GLUT1 deficiency syndrome 2 SLC2A1* Slc2a1   Alliance of Genome Resources
choreatic disease NKX2-1* Nkx2-1   Alliance of Genome Resources
chromosome 3-linked frontotemporal dementia CHMP2B* Chmp2b 2 models Alliance of Genome Resources
complex cortical dysplasia with other brain malformations 1 TUBB3* Tubb3   Alliance of Genome Resources
complex cortical dysplasia with other brain malformations 2 KIF5C* Kif5c   Alliance of Genome Resources
complex cortical dysplasia with other brain malformations 3 KIF2A* Kif2a   Alliance of Genome Resources
complex cortical dysplasia with other brain malformations 4 TUBG1* Tubg1   Alliance of Genome Resources
complex cortical dysplasia with other brain malformations 5 TUBB2A* Tubb2a   Alliance of Genome Resources
complex cortical dysplasia with other brain malformations 6 TUBB* Tubb5   Alliance of Genome Resources
Creutzfeldt-Jakob disease HLA-DQB1*, HLA-DQB2 H2-Ab1   Alliance of Genome Resources
dentatorubral-pallidoluysian atrophy ATN1* Atn1 5 models Alliance of Genome Resources
developmental and epileptic encephalopathy 1 ARX* Arx   Alliance of Genome Resources
developmental and epileptic encephalopathy 11 SCN2A* Scn2a   Alliance of Genome Resources
developmental and epileptic encephalopathy 12 PLCB1* Plcb1   Alliance of Genome Resources
developmental and epileptic encephalopathy 13 SCN8A* Scn8a   Alliance of Genome Resources
developmental and epileptic encephalopathy 14 KCNT1* Kcnt1   Alliance of Genome Resources
developmental and epileptic encephalopathy 15 ST3GAL3* St3gal3   Alliance of Genome Resources
developmental and epileptic encephalopathy 18 SZT2* Szt2   Alliance of Genome Resources
developmental and epileptic encephalopathy 19 GABRA1* Gabra1   Alliance of Genome Resources
developmental and epileptic encephalopathy 21 NECAP1* Necap1   Alliance of Genome Resources
developmental and epileptic encephalopathy 23 DOCK7* Dock7   Alliance of Genome Resources
developmental and epileptic encephalopathy 24 HCN1* Hcn1   Alliance of Genome Resources
developmental and epileptic encephalopathy 25 SLC13A5* Slc13a5   Alliance of Genome Resources
developmental and epileptic encephalopathy 26 KCNB1* Kcnb1   Alliance of Genome Resources
developmental and epileptic encephalopathy 27 GRIN2B* Grin2b   Alliance of Genome Resources
developmental and epileptic encephalopathy 28 WWOX* Wwox   Alliance of Genome Resources
developmental and epileptic encephalopathy 29 AARS1* Aars   Alliance of Genome Resources
developmental and epileptic encephalopathy 3 SLC25A22* Slc25a22   Alliance of Genome Resources
developmental and epileptic encephalopathy 30 SIK1* Sik1   Alliance of Genome Resources
developmental and epileptic encephalopathy 31 DNM1* Dnm1   Alliance of Genome Resources
developmental and epileptic encephalopathy 32 KCNA2* Kcna2   Alliance of Genome Resources
developmental and epileptic encephalopathy 33 EEF1A2* Eef1a2   Alliance of Genome Resources
developmental and epileptic encephalopathy 34 SLC12A5* Slc12a5   Alliance of Genome Resources
developmental and epileptic encephalopathy 35 ITPA* Itpa   Alliance of Genome Resources
developmental and epileptic encephalopathy 36 ALG13* Alg13   Alliance of Genome Resources
developmental and epileptic encephalopathy 37 FRRS1L* Frrs1l   Alliance of Genome Resources
developmental and epileptic encephalopathy 38 ARV1* Arv1   Alliance of Genome Resources
developmental and epileptic encephalopathy 4 STXBP1* Stxbp1   Alliance of Genome Resources
developmental and epileptic encephalopathy 40 GUF1* Guf1   Alliance of Genome Resources
developmental and epileptic encephalopathy 41 SLC1A2* Slc1a2   Alliance of Genome Resources
developmental and epileptic encephalopathy 42 CACNA1A* Cacna1a   Alliance of Genome Resources
developmental and epileptic encephalopathy 43 GABRB3* Gabrb3   Alliance of Genome Resources
developmental and epileptic encephalopathy 44 UBA5* Uba5   Alliance of Genome Resources
developmental and epileptic encephalopathy 45 GABRB1* Gabrb1   Alliance of Genome Resources
developmental and epileptic encephalopathy 46 GRIN2D* Grin2d   Alliance of Genome Resources
developmental and epileptic encephalopathy 47 FGF12* Fgf12   Alliance of Genome Resources
developmental and epileptic encephalopathy 48 AP3B2* Ap3b2   Alliance of Genome Resources
developmental and epileptic encephalopathy 49 DENND5A* Dennd5a   Alliance of Genome Resources
developmental and epileptic encephalopathy 5 SPTAN1* Sptan1   Alliance of Genome Resources
developmental and epileptic encephalopathy 50 CAD* Cad   Alliance of Genome Resources
developmental and epileptic encephalopathy 51 MDH2* Mdh2   Alliance of Genome Resources
developmental and epileptic encephalopathy 52 SCN1B* Scn1b   Alliance of Genome Resources
developmental and epileptic encephalopathy 53 SYNJ1* Synj1   Alliance of Genome Resources
developmental and epileptic encephalopathy 54 HNRNPU* Hnrnpu   Alliance of Genome Resources
developmental and epileptic encephalopathy 55 PIGP* Pigp   Alliance of Genome Resources
developmental and epileptic encephalopathy 56 YWHAG* Ywhag   Alliance of Genome Resources
developmental and epileptic encephalopathy 57 KCNT2* Kcnt2   Alliance of Genome Resources
developmental and epileptic encephalopathy 58 NTRK2* Ntrk2   Alliance of Genome Resources
developmental and epileptic encephalopathy 59 GABBR2* Gabbr2   Alliance of Genome Resources
developmental and epileptic encephalopathy 60 CNPY3* Cnpy3   Alliance of Genome Resources
developmental and epileptic encephalopathy 61 ADAM22* Adam22   Alliance of Genome Resources
developmental and epileptic encephalopathy 62 SCN3A* Scn3a   Alliance of Genome Resources
developmental and epileptic encephalopathy 63 CPLX1* Cplx1   Alliance of Genome Resources
developmental and epileptic encephalopathy 65 CYFIP2* Cyfip2   Alliance of Genome Resources
developmental and epileptic encephalopathy 66 PACS2* Pacs2   Alliance of Genome Resources
developmental and epileptic encephalopathy 67 CUX2* Cux2   Alliance of Genome Resources
developmental and epileptic encephalopathy 68 TRAK1* Trak1   Alliance of Genome Resources
developmental and epileptic encephalopathy 69 CACNA1E* Cacna1e   Alliance of Genome Resources
developmental and epileptic encephalopathy 70 PHACTR1* Phactr1   Alliance of Genome Resources
developmental and epileptic encephalopathy 71 GLS* Gls   Alliance of Genome Resources
developmental and epileptic encephalopathy 72 NEUROD2* Neurod2   Alliance of Genome Resources
developmental and epileptic encephalopathy 73 RNF13* Rnf13   Alliance of Genome Resources
developmental and epileptic encephalopathy 74 GABRG2* Gabrg2   Alliance of Genome Resources
developmental and epileptic encephalopathy 75 PARS2* Pars2   Alliance of Genome Resources
developmental and epileptic encephalopathy 76 ACTL6B* Actl6b   Alliance of Genome Resources
developmental and epileptic encephalopathy 77 PIGQ* Pigq   Alliance of Genome Resources
developmental and epileptic encephalopathy 78 GABRA2* Gabra2   Alliance of Genome Resources
developmental and epileptic encephalopathy 79 GABRA5* Gabra5   Alliance of Genome Resources
developmental and epileptic encephalopathy 8 ARHGEF9* Arhgef9   Alliance of Genome Resources
developmental and epileptic encephalopathy 80 PIGB* Pigb   Alliance of Genome Resources
developmental and epileptic encephalopathy 81 DMXL2* Dmxl2   Alliance of Genome Resources
developmental and epileptic encephalopathy 82 GOT2* Got2   Alliance of Genome Resources
developmental and epileptic encephalopathy 83 UGP2* Ugp2   Alliance of Genome Resources
developmental and epileptic encephalopathy 84 UGDH* Ugdh   Alliance of Genome Resources
developmental and epileptic encephalopathy 86 DALRD3* Dalrd3   Alliance of Genome Resources
developmental and epileptic encephalopathy 87 CDK19* Cdk19   Alliance of Genome Resources
developmental and epileptic encephalopathy 88 MDH1* Mdh1   Alliance of Genome Resources
developmental and epileptic encephalopathy 89 GAD1* Gad1   Alliance of Genome Resources
developmental and epileptic encephalopathy 9 PCDH19* Pcdh19   Alliance of Genome Resources
developmental and epileptic encephalopathy 91 PPP3CA* Ppp3ca   Alliance of Genome Resources
developmental and epileptic encephalopathy 92 GABRB2* Gabrb2   Alliance of Genome Resources
developmental and epileptic encephalopathy 93 ATP6V1A* Atp6v1a   Alliance of Genome Resources
dystonia 12 ATP1A3* Atp1a3   Alliance of Genome Resources
dystonia 16 PRKRA* Prkra   Alliance of Genome Resources
dystonia 24 ANO3* Ano3   Alliance of Genome Resources
dystonia 25 GNAL* Gnal   Alliance of Genome Resources
dystonia 27 COL6A3* Col6a3   Alliance of Genome Resources
dystonia 5 GCH1* Gch1   Alliance of Genome Resources
dystonia 9 SLC2A1* Slc2a1   Alliance of Genome Resources
early-onset vitamin B6-dependent epilepsy PLPBP* Plpbp   Alliance of Genome Resources
essential tremor 1 DRD3* Drd3   Alliance of Genome Resources
essential tremor 4 FUS* Fus   Alliance of Genome Resources
essential tremor 5 TENM4* Tenm4   Alliance of Genome Resources
familial adult myoclonic epilepsy 1 SAMD12* Samd12   Alliance of Genome Resources
familial adult myoclonic epilepsy 2 STARD7* Stard7   Alliance of Genome Resources
familial adult myoclonic epilepsy 3 MARCHF6* Marchf6   Alliance of Genome Resources
familial adult myoclonic epilepsy 4 YEATS2* Yeats2   Alliance of Genome Resources
familial adult myoclonic epilepsy 5 CNTN2* Cntn2   Alliance of Genome Resources
familial adult myoclonic epilepsy 6 TNRC6A* Tnrc6a   Alliance of Genome Resources
familial adult myoclonic epilepsy 7 RAPGEF2* Rapgef2   Alliance of Genome Resources
familial febrile seizures 11 CPA6* Cpa6   Alliance of Genome Resources
familial febrile seizures 2 HCN2* Hcn2   Alliance of Genome Resources
familial febrile seizures 4 ADGRV1* Adgrv1   Alliance of Genome Resources
familial febrile seizures 8 GABRG2* Gabrg2   Alliance of Genome Resources
familial hemiplegic migraine 1 CACNA1A* Cacna1a   Alliance of Genome Resources
familial hemiplegic migraine 3 SCN1A* Scn1a   Alliance of Genome Resources
familial temporal lobe epilepsy 1 RELN* Reln   Alliance of Genome Resources
familial temporal lobe epilepsy 1 MICAL1* Mical1   Alliance of Genome Resources
familial temporal lobe epilepsy 5 CPA6* Cpa6   Alliance of Genome Resources
familial temporal lobe epilepsy 7 RELN* Reln   Alliance of Genome Resources
familial temporal lobe epilepsy 8 GAL* Gal   Alliance of Genome Resources
Friedreich ataxia 1 FXN* Fxn   Alliance of Genome Resources
frontotemporal dementia MAPT* Mapt 17 models Alliance of Genome Resources
frontotemporal dementia PSEN1* Psen1   Alliance of Genome Resources
generalized epilepsy with febrile seizures plus 1 SCN1B* Scn1b   Alliance of Genome Resources
generalized epilepsy with febrile seizures plus 10 HCN1* Hcn1   Alliance of Genome Resources
generalized epilepsy with febrile seizures plus 2 SCN1A* Scn1a   Alliance of Genome Resources
generalized epilepsy with febrile seizures plus 9 STX1B* Stx1b   Alliance of Genome Resources
Huntington's disease-like 1 PRNP* Prnp   Alliance of Genome Resources
hydrocephalus MPDZ* Mpdz   Alliance of Genome Resources
hydrocephalus L1CAM* L1cam   Alliance of Genome Resources
hydrocephalus CCDC88C* Ccdc88c   Alliance of Genome Resources
hypomyelinating leukodystrophy 10 PYCR2* Pycr2   Alliance of Genome Resources
hypomyelinating leukodystrophy 11 POLR1C* Polr1c   Alliance of Genome Resources
hypomyelinating leukodystrophy 12 VPS11* Vps11   Alliance of Genome Resources
hypomyelinating leukodystrophy 13 HIKESHI* Hikeshi   Alliance of Genome Resources
hypomyelinating leukodystrophy 14 UFM1* Ufm1   Alliance of Genome Resources
hypomyelinating leukodystrophy 20 CNP* Cnp   Alliance of Genome Resources
hypomyelinating leukodystrophy 3 AIMP1* Aimp1   Alliance of Genome Resources
hypomyelinating leukodystrophy 4 HSPD1* Hspd1   Alliance of Genome Resources
hypomyelinating leukodystrophy 5 FAM126A* Fam126a   Alliance of Genome Resources
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism POLR3B* Polr3b   Alliance of Genome Resources
hypomyelinating leukodystrophy 7 with or without oligodontia and-or hypogonadotropic hypogonadism POLR3A* Polr3a 2 "NOT" models Alliance of Genome Resources
hypomyelinating leukodystrophy 8 with or without oligodontia and-or hypogonadotropic hypogonadism POLR3B* Polr3b   Alliance of Genome Resources
hypomyelinating leukodystrophy 9 RARS1* Rars   Alliance of Genome Resources
idiopathic generalized epilepsy 10 GABRD* Gabrd   Alliance of Genome Resources
idiopathic generalized epilepsy 11 CLCN2* Clcn2   Alliance of Genome Resources
idiopathic generalized epilepsy 12 SLC2A1* Slc2a1   Alliance of Genome Resources
idiopathic generalized epilepsy 13 GABRA1* Gabra1   Alliance of Genome Resources
idiopathic generalized epilepsy 14 SLC12A5* Slc12a5   Alliance of Genome Resources
idiopathic generalized epilepsy 15 RORB* Rorb   Alliance of Genome Resources
idiopathic generalized epilepsy 8 CASR* Casr   Alliance of Genome Resources
idiopathic generalized epilepsy 9 CACNB4* Cacnb4   Alliance of Genome Resources
infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly MED17* Med17   Alliance of Genome Resources
intracranial berry aneurysm 12 THSD1* Thsd1   Alliance of Genome Resources
Joubert syndrome 1 INPP5E* Inpp5e   Alliance of Genome Resources
Joubert syndrome 10 OFD1* Ofd1   Alliance of Genome Resources
Joubert syndrome 13 TCTN1* Tctn1   Alliance of Genome Resources
Joubert syndrome 14 TMEM237* Tmem237   Alliance of Genome Resources
Joubert syndrome 15 CEP41* Cep41   Alliance of Genome Resources
Joubert syndrome 16 TMEM138* Tmem138   Alliance of Genome Resources
Joubert syndrome 18 TCTN3* Tctn3   Alliance of Genome Resources
Joubert syndrome 2 TMEM216* Tmem216   Alliance of Genome Resources
Joubert syndrome 20 TMEM231* Tmem231   Alliance of Genome Resources
Joubert syndrome 21 CSPP1* Cspp1   Alliance of Genome Resources
Joubert syndrome 22 PDE6D* Pde6d   Alliance of Genome Resources
Joubert syndrome 23 KIAA0586* 2700049A03Rik   Alliance of Genome Resources
Joubert syndrome 24 TCTN2* Tctn2   Alliance of Genome Resources
Joubert syndrome 25 CEP104* Cep104   Alliance of Genome Resources
Joubert syndrome 27 B9D1* B9d1   Alliance of Genome Resources
Joubert syndrome 28 MKS1* Mks1   Alliance of Genome Resources
Joubert syndrome 30 ARMC9* Armc9   Alliance of Genome Resources
Joubert syndrome 31 CEP120* Cep120   Alliance of Genome Resources
Joubert syndrome 32 SUFU* Sufu   Alliance of Genome Resources
Joubert syndrome 33 PIBF1* Pibf1   Alliance of Genome Resources
Joubert syndrome 4 NPHP1* Nphp1   Alliance of Genome Resources
Joubert syndrome 8 ARL13B* Arl13b   Alliance of Genome Resources
Joubert syndrome 9 CC2D2A* Cc2d2a   Alliance of Genome Resources
Joubert syndrome with orofaciodigital defect CPLANE1* Cplane1   Alliance of Genome Resources
juvenile absence epilepsy 1 EFHC1* Efhc1   Alliance of Genome Resources
juvenile myoclonic epilepsy 10 CILK1* Cilk1   Alliance of Genome Resources
Landau-Kleffner syndrome GRIN2A* Grin2a   Alliance of Genome Resources
leukoencephalopathy with vanishing white matter EIF2B3* Eif2b3   Alliance of Genome Resources
leukoencephalopathy with vanishing white matter EIF2B1* Eif2b1   Alliance of Genome Resources
leukoencephalopathy with vanishing white matter EIF2B2* Eif2b2   Alliance of Genome Resources
Machado-Joseph disease ATXN3* Atxn3 17 models Alliance of Genome Resources
medulloblastoma BRCA2* Brca2 2 models Alliance of Genome Resources
medulloblastoma CTNNB1* Ctnnb1   Alliance of Genome Resources
medulloblastoma ELP1* Elp1   Alliance of Genome Resources
medulloblastoma PTCH2* Ptch2 2 models Alliance of Genome Resources
medulloblastoma SUFU* Sufu 1 model Alliance of Genome Resources
megalencephalic leukoencephalopathy with subcortical cysts 1 HEPACAM* Hepacam   Alliance of Genome Resources
megalencephalic leukoencephalopathy with subcortical cysts 2A HEPACAM* Hepacam   Alliance of Genome Resources
megalencephalic leukoencephalopathy with subcortical cysts 2B HEPACAM* Hepacam   Alliance of Genome Resources
microcephaly, seizures, and developmental delay PNKP* Pnkp   Alliance of Genome Resources
migraine EDNRA* Ednra   Alliance of Genome Resources
migraine ESR1* Esr1   Alliance of Genome Resources
migraine TNF* Tnf   Alliance of Genome Resources
Moyamoya disease ACTA2* Acta2   Alliance of Genome Resources
Moyamoya disease RNF213* Rnf213 1 "NOT" model Alliance of Genome Resources
Moyamoya disease GUCY1A1* Gucy1a1   Alliance of Genome Resources
myoclonic dystonia 26 KCTD17* Kctd17   Alliance of Genome Resources
nonprogressive cerebellar ataxia with mental retardation CAMTA1* Camta1   Alliance of Genome Resources
PEHO syndrome ZNHIT3* Znhit3   Alliance of Genome Resources
progressive myoclonus epilepsy 10 PRDM8* Prdm8   Alliance of Genome Resources
progressive myoclonus epilepsy 1A CSTB* Cstb   Alliance of Genome Resources
progressive myoclonus epilepsy 3 KCTD7* Kctd7   Alliance of Genome Resources
progressive myoclonus epilepsy 4 SCARB2* Scarb2   Alliance of Genome Resources
progressive myoclonus epilepsy 6 GOSR2* Gosr2   Alliance of Genome Resources
progressive myoclonus epilepsy 7 KCNC1* Kcnc1   Alliance of Genome Resources
progressive myoclonus epilepsy 8 CERS1* Cers1   Alliance of Genome Resources
progressive myoclonus epilepsy 9 LMNB2* Lmnb2   Alliance of Genome Resources
progressive supranuclear palsy MAPT* Mapt   Alliance of Genome Resources
RNASET2-deficient cystic leukoencephalopathy RNASET2* Rnaset2a, Rnaset2b   Alliance of Genome Resources
Rolandic epilepsy-paroxysmal exercise-induced dystonia-writer's cramp syndrome TBC1D24* Tbc1d24   Alliance of Genome Resources
sepiapterin reductase deficiency SPR* Spr   Alliance of Genome Resources
severe congenital encephalopathy due to MECP2 mutation MECP2* Mecp2   Alliance of Genome Resources
spastic quadriplegia KANK1* Kank1   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 1 ATXN1* Atxn1 3 models Alliance of Genome Resources
spinocerebellar ataxia type 10 ATXN10* Atxn10 1 model 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 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 40 CCDC88C* Ccdc88c   Alliance of Genome Resources
spinocerebellar ataxia type 8 ATXN8OS*  
spinocerebellar ataxia type 8 ATXN8*  
torsion dystonia 2 HPCA* Hpca   Alliance of Genome Resources
torsion dystonia 4 TUBB4A* Tubb4a   Alliance of Genome Resources
X-linked dystonia-parkinsonism TAF1*, TAF1L Taf1   Alliance of Genome Resources
X-linked epilepsy with variable learning disabilities and behavior disorders SYN1* Syn1   Alliance of Genome Resources
X-linked parkinsonism-spasticity syndrome ATP6AP2* Atp6ap2   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
  adult-onset autosomal dominant demyelinating leukodystrophy Tg(Plp1-LMNB1)1108Qsp 1 model
  adult-onset autosomal dominant demyelinating leukodystrophy Tg(Lmnb1)1Yfu 1 model
  adult-onset autosomal dominant demyelinating leukodystrophy Tg(Plp1-Lmnb1)#Yfu 1 model
  Alexander disease Tg(GFAP)10Mes 3 models
  Alexander disease Tg(Gfap-GFAP*R239H)60TMIke 1 model
  Alexander disease Tg(GFAP)7Mes 1 model
  arteriovenous malformations of the brain Tg(tetO-Notch4*)1Rwng 1 model
  autosomal dominant nocturnal frontal lobe epilepsy 3 Tg(tetO-Chrnb2*V287L)H3Gica 1 model
  brain ischemia Tg(Notch3*R169C)88Bbb 1 model
  CADASIL 1 Tg(Notch3*R169C)88Bbb 1 model
  Creutzfeldt-Jakob disease Tg(Prnp*)#Rgab 2 models
  Creutzfeldt-Jakob disease Tg(Prnp*D177N*M128V)A21Rchi 4 models
  dentatorubral-pallidoluysian atrophy Tg(ATN1*)Q129Stsu 1 model
  dentatorubral-pallidoluysian atrophy Tg(Prnp-ATN1)150Dbo 1 model
  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
  epilepsy Tg(RP23-65I14)1Jno 1 model
  epilepsy Tg(RP23-65I14)2Jno 1 model
  epilepsy Tg(Eno2-Scn2a1*)Q54Mm 3 models
  epilepsy Tg(Camk2a-Bdnf)A9Stl 1 model
  familial temporal lobe epilepsy 1 Tg(Lgi1*)#Mpan 1 model
  frontotemporal dementia Tg(Tuba1-MAPT)14Vle 1 model
  frontotemporal dementia Tg(Thy1-TARDBP)6Singh 1 model
  frontotemporal dementia Tg(Thy1-TARDBP)4Singh 2 models
  frontotemporal dementia Tg(Thy1-MAPT*V337M)1Godt 1 model
  frontotemporal dementia Tg(Thy1-MAPT*P301S)2541Godt 1 model
  frontotemporal dementia Tg(Thy1-MAPT*K369I)K3Gotz 1 model
  frontotemporal dementia Tg(Thy1-MAPT*)1Avil 1 model
  frontotemporal dementia Tg(tetO-CHMP2B*)3Fbga 1 model
  frontotemporal dementia Tg(Prnp-TARDBP*A315T)95Balo 1 model
  frontotemporal dementia Tg(Prnp-MAPT*R406W)21807Dwst 1 model
  frontotemporal dementia Tg(Prnp-MAPT*P301S)50Hiw 1 model
  frontotemporal dementia Tg(Prnp-MAPT*P301L)JNPL3Hlmc 1 model
  frontotemporal dementia Tg(Prnp-MAPT)43Vle 1 model
  frontotemporal dementia Tg(Prnp-MAPT)7Vle 1 model
  frontotemporal dementia Tg(PDGFB-MAPT*V337M)1Atak 1 model
  frontotemporal dementia Tg(MAPT*V337M)1Gds 1 model
  frontotemporal dementia Tg(Camk2a-MAPT*R406W)748Atak 1 model
  frontotemporal dementia Tg(Camk2a-MAPT*P301L)D35Jiri 1 model
  frontotemporal dementia Tg(Camk2a-MAPT)601Ymot 1 model
  generalized epilepsy with febrile seizures plus Tg(Scn1a*)RH9Aesc 1 model
  Gerstmann-Straussler-Scheinker syndrome Tg(Prnp*P101L)2862Sbp 1 model
  Gerstmann-Straussler-Scheinker syndrome Tg(Prnp*P101L)2247Sbp 1 model
  Gerstmann-Straussler-Scheinker syndrome Tg(Prnp*P101L)174Sbp 1 model
  Gerstmann-Straussler-Scheinker syndrome Tg(Prnp*A116V*M128V)1309Jama 1 model
  Gerstmann-Straussler-Scheinker syndrome Tg(Prnp*P101L)2866Sbp 3 models
  Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Tg(TARDBP*A315T)#Jpj 1 model
  Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Tg(Camk2a-Tardbp)#Ckjs 1 model
  Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Tg(Prnp-TARDBP)3cPtrc 1 model
  Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Tg(TARDBP)#Jpj 1 model
  Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Tg(TARDBP*G348C)#Jpj 1 model
  Grn-related frontotemporal lobar degeneration with Tdp43 inclusions Tg(Thy1-TARDBP*)BOddo 2 models
  hydrocephalus Tg(Sox3)1Pqt 1 model
  Lafora disease Tg(CAG-EPM2A*C266S)1Bmin 1 model
  leukoencephalopathy with vanishing white matter Tg(Plp1-Eif2ak3*)18Pop 1 model
  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(ATXN3*)84.2Cce 3 models
  Machado-Joseph disease Tg(Prnp-ATXN3*148Q)148.19Olri 1 model
  Machado-Joseph disease Tg(ATXN3*)67.2Cce 2 models
  Machado-Joseph disease Tg(Prnp-ATXN3*148Q)NLS.28Olri 1 model
  medulloblastoma Tg(Neurod2-Smo*A2)#Jols 1 model
  medulloblastoma Tg(Neurod2-Smo*A1)199Jols 3 models
  medulloblastoma Tg(tetO-Ifng)184Pop 2 models
  medulloblastoma Tg(tetO-MYCN,-luc)#Waw 2 models
  medulloblastoma Tg(tetO-TAg,CMV-rtTA)123Yihu 1 model
  paroxysmal nonkinesigenic dyskinesia 1 Tg(Pnkd*A7V*A9V,-DsRed)704Ljp 1 model
  paroxysmal nonkinesigenic dyskinesia 1 Tg(Pnkd*A7V*A9V,-DsRed)671Ljp 1 model
  Pelizaeus-Merzbacher disease Dp(XTceal3-Plp1)1Gmh 1 model
  Pelizaeus-Merzbacher disease Tg(Plp)72Kan 1 model
  Pelizaeus-Merzbacher disease Tg(Plp)66Kan 2 models
  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*)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 17 Tg(Prnp-TBP*)71-27Xjl 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)2521Als 1 model
  spinocerebellar ataxia type 7 Tg(GFAP-ATXN7*92Q)2542Als 1 model
  spinocerebellar ataxia type 7 Tg(Pcp2-SCA7)P7EJman 1 model
  spinocerebellar ataxia type 7 Tg(Prnp-ATXN7*92Q)1963Als 1 model
  spinocerebellar ataxia type 7 Tg(RHO-SCA7)R7EJman 1 model
  torsion dystonia 1 Tg(Eno2-TOR1A*)13Shas 1 model
  torsion dystonia 1 Tg(CMV-TOR1A*)2Nush 1 model
  torsion dystonia 1 Tg(CMV-TOR1A*)1Nush 1 model