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* | 1 model | Alliance of Genome Resources | |||
Alexander disease | GFAP* | Gfap* | 4 models | Alliance of Genome Resources | |||
arteriovenous malformations of the brain | KRAS* | Kras* | 2 models | Alliance of Genome Resources | |||
arteriovenous malformations of the brain | ENG* | Eng* | 1 model | 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 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 | |||
basal ganglia calcification | PDGFRB* | Pdgfrb* | 1 model | Alliance of Genome Resources | |||
basal ganglia calcification | SLC20A2* | Slc20a2* | 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* | 6 models | Alliance of Genome Resources | |||
Canavan disease | ASPA* | Aspa* | 5 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 | KRIT1* | Krit1* | 1 model | 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 4 | TUBG1* | Tubg1* | 1 model | 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 | |||
Dandy-Walker syndrome | ZIC1* | Zic1* | 1 model | Alliance of Genome Resources | |||
developmental and epileptic encephalopathy 14 | KCNT1* | Kcnt1* | 2 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 54 | HNRNPU* | Hnrnpu* | 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 | |||
Friedreich ataxia | FXN* | Fxn* | 8 models | Alliance of Genome Resources | |||
frontotemporal dementia | CHMP2B* | Chmp2b* | 1 model | Alliance of Genome Resources | |||
generalized epilepsy with febrile seizures plus | SCN1A* | Scn1a* | 5 models | 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 | |||
hydrocephalus | TRIM71* | Trim71* | 1 model | 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 | |||
leukoencephalopathy with vanishing white matter | EIF2B5* | Eif2b5* | 7 models | Alliance of Genome Resources | |||
MASA syndrome | L1CAM* | L1cam* | 1 model | 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* | 8 models | Alliance of Genome Resources | |||
progressive myoclonus epilepsy 1B | PRICKLE1* | Prickle1* | 1 model | 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 | |||
torsion dystonia 1 | TOR1A* | Tor1a* | 4 models | Alliance of Genome Resources | |||
torsion dystonia 6 | THAP1* | Thap1* | 2 models | Alliance of Genome Resources | |||
Unverricht-Lundborg syndrome | CSTB* | Cstb* | 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 | |||
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 | 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 | GOT2 | Got2* | 2 models | Alliance of Genome Resources | |||
early infantile epileptic encephalopathy | SCN8A | Scn8a* | 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 | |||
epilepsy | KCNA1 | Kcna1* | 1 model | Alliance of Genome Resources | |||
epilepsy | GAD2 | Gad2* | 1 model | Alliance of Genome Resources | |||
epilepsy | CDYL | Cdyl* | 1 model | Alliance of Genome Resources | |||
epilepsy | CACNA2D2 | Cacna2d2* | 1 model | Alliance of Genome Resources | |||
epilepsy | C1QA | C1qa* | 1 model | Alliance of Genome Resources | |||
epilepsy | BSN | Bsn* | 1 model | Alliance of Genome Resources | |||
epilepsy | ATP6V1B2 | Atp6v1b2* | 1 model | Alliance of Genome Resources | |||
epilepsy | ALDH5A1 | Aldh5a1* | 1 model | Alliance of Genome Resources | |||
epilepsy | SCAMP5 | Scamp5* | 1 model | 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 | |||
frontotemporal dementia | VCP | Vcp* | 1 model | Alliance of Genome Resources | |||
frontotemporal dementia | TREM2 | Trem2* | 1 model | Alliance of Genome Resources | |||
frontotemporal dementia | TARDBP | Tardbp* | 2 models | Alliance of Genome Resources | |||
generalized dystonia | CACNA1A | Cacna1a* | 2 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* | 1 model | Alliance of Genome Resources | |||
hydrocephalus | ADD1 | Add1* | 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 | |||
hydrocephalus | E2F5 | E2f5* | 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 | AK8 | Ak8* | 1 model | Alliance of Genome Resources | |||
hydrocephalus | AK7 | Ak7* | 1 model | Alliance of Genome Resources | |||
idiopathic generalized epilepsy | GABRA1 | Gabra1* | 3 models | Alliance of Genome Resources | |||
idiopathic generalized epilepsy | DNM1 | Dnm1* | 2 models | Alliance of Genome Resources | |||
Joubert syndrome | ZIC1 | Zic1* | 1 model | Alliance of Genome Resources | |||
Lafora disease | NHLRC1 | Nhlrc1* | 3 models | Alliance of Genome Resources | |||
Lafora disease | EPM2A | Epm2a* | 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 | |||
leukoencephalopathy with vanishing white matter | EIF2B4 | Eif2b4* | 4 models | Alliance of Genome Resources | |||
medulloblastoma | IFNG | Ifng* | 2 models | Alliance of Genome Resources | |||
medulloblastoma | SMO | Smo* | 8 models | Alliance of Genome Resources | |||
medulloblastoma | PTCH1 | Ptch1* | 12 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 | CWH43 | Cwh43* | 3 models | Alliance of Genome Resources | |||
normal pressure hydrocephalus | AK9 | Ak9* | 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 | |||
pyridoxine-dependent epilepsy | ALDH7A1 | Aldh7a1* | 1 model | Alliance of Genome Resources | |||
spinocerebellar ataxia type 27 | FGF14 | Fgf14* | 1 model | Alliance of Genome Resources | |||
Stiff-Person syndrome | TRAK1 | Trak1* | 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 | |||
temporal lobe epilepsy | GLUL | Glul* | 1 model | Alliance of Genome Resources | |||
adult-onset leukoencephalopathy with axonal spheroids and pigmented glia | CSF1R* | Csf1r | Alliance of Genome Resources | ||||
alveolar echinococcosis | HLA-DRB1*, HLA-DRB3, HLA-DRB4, HLA-DRB5 | H2-Eb1, H2-Eb2 | Alliance of Genome Resources | ||||
alveolar echinococcosis | HLA-DQB1*, HLA-DQB2 | H2-Ab1 | Alliance of Genome Resources | ||||
arteriovenous malformations of the brain | IL6* | Il6 | Alliance of Genome Resources | ||||
ataxia-oculomotor apraxia type 4 | PNKP* | Pnkp | Alliance of Genome Resources | ||||
ataxia telangiectasia | BIK* | Bik | Alliance of Genome Resources | ||||
ataxia telangiectasia | BAK1* | Bak1 | Alliance of Genome Resources | ||||
ataxia telangiectasia | BAX* | Bax | Alliance of Genome Resources | ||||
ataxia telangiectasia | HDAC4* | Hdac4 | Alliance of Genome Resources | ||||
ataxia telangiectasia | IFNG* | Ifng | Alliance of Genome Resources | ||||
ataxia telangiectasia | IL2* | Il2 | 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 | NPTX1* | Nptx1 | Alliance of Genome Resources | ||||
autosomal dominant cerebellar ataxia | FGF14* | Fgf14 | Alliance of Genome Resources | ||||
autosomal dominant cerebellar ataxia | SAMD9L* | Samd9l | Alliance of Genome Resources | ||||
autosomal dominant cerebellar ataxia, deafness and narcolepsy | DNMT1* | Dnmt1 | Alliance of Genome Resources | ||||
autosomal dominant nocturnal frontal lobe epilepsy | CHRNB2* | Chrnb2 | 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 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 | ||||
basal ganglia calcification | XPR1* | Xpr1 | Alliance of Genome Resources | ||||
basal ganglia calcification | MYORG* | Myorg | Alliance of Genome Resources | ||||
basal ganglia calcification | JAM2* | Jam2 | Alliance of Genome Resources | ||||
basal ganglia calcification | PDGFB* | Pdgfb | Alliance of Genome Resources | ||||
basal ganglia disease | FTL* | Ftl1, Ftl1-ps2, Ftl2-ps | Alliance of Genome Resources | ||||
benign familial infantile seizures 2 | PRRT2* | Prrt2 | Alliance of Genome Resources | ||||
benign familial infantile seizures 3 | SCN2A* | Scn2a | Alliance of Genome Resources | ||||
benign familial infantile seizures 5 | SCN8A* | Scn8a | Alliance of Genome Resources | ||||
benign familial infantile seizures 6 | CHRNA2* | Chrna2 | Alliance of Genome Resources | ||||
benign neonatal seizures | ATP1A2* | Atp1a2 | 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 | ||||
blepharospasm | DRD5* | Drd5 | Alliance of Genome Resources | ||||
brain cancer | TERT* | Tert | Alliance of Genome Resources | ||||
brain cancer | CCDC26* | ||||||
brain cancer | CDKN2B-AS1* | ||||||
brain disease | TRAF3* | Traf3 | Alliance of Genome Resources | ||||
brain disease | UNC93B1* | Unc93b1 | Alliance of Genome Resources | ||||
brain disease | TICAM1* | Ticam1 | Alliance of Genome Resources | ||||
brain disease | TBK1* | Tbk1 | Alliance of Genome Resources | ||||
brain disease | SNORA31* | ||||||
brain disease | RANBP2*, RGPD1, RGPD2, RGPD3, RGPD4, RGPD5, RGPD6, RGPD8 | Ranbp2 | Alliance of Genome Resources | ||||
brain disease | PPP2R2B* | Ppp2r2b | Alliance of Genome Resources | ||||
brain disease | NUP214* | Nup214 | Alliance of Genome Resources | ||||
brain disease | MFF* | Mff | Alliance of Genome Resources | ||||
brain disease | IRF3* | Irf3 | Alliance of Genome Resources | ||||
brain disease | DBR1* | Dbr1 | Alliance of Genome Resources | ||||
brain disease | CPT2* | Cpt2 | Alliance of Genome Resources | ||||
brain edema | SERPINF1* | Serpinf1 | Alliance of Genome Resources | ||||
brain glioma | XRCC3* | Xrcc3 | Alliance of Genome Resources | ||||
brain glioma | ADAM3A* | Adam3 | Alliance of Genome Resources | ||||
brain glioma | PTPRB* | Ptprb | Alliance of Genome Resources | ||||
brain glioma | XRCC1* | Xrcc1 | Alliance of Genome Resources | ||||
brain infarction | HLA-DQA1*, HLA-DQA2 | H2-Aa | Alliance of Genome Resources | ||||
brain infarction | CYP2R1* | Cyp2r1 | Alliance of Genome Resources | ||||
brain infarction | ALDH2* | Aldh2 | Alliance of Genome Resources | ||||
brain infarction | CFH* | Cfh, Cfhr4 | Alliance of Genome Resources | ||||
brain infarction | ADM* | Adm | Alliance of Genome Resources | ||||
brain infarction | ALOX5AP* | Alox5ap | Alliance of Genome Resources | ||||
brain ischemia | SELE* | Sele | Alliance of Genome Resources | ||||
brain ischemia | ANGPT1* | Angpt1 | Alliance of Genome Resources | ||||
brain ischemia | ANXA1* | Anxa1 | Alliance of Genome Resources | ||||
brain ischemia | CSF3* | Csf3 | Alliance of Genome Resources | ||||
brain ischemia | FGF1* | Fgf1 | Alliance of Genome Resources | ||||
brain ischemia | HSPA1B*, HSPA1A | Hspa1a, Hspa1b | Alliance of Genome Resources | ||||
brain ischemia | IGF1* | Igf1 | Alliance of Genome Resources | ||||
brain ischemia | MDK* | Mdk | Alliance of Genome Resources | ||||
brain ischemia | PGF* | Pgf | Alliance of Genome Resources | ||||
brain ischemia | PROZ* | Proz | Alliance of Genome Resources | ||||
brain small vessel disease | NR1D1* | Nr1d1 | Alliance of Genome Resources | ||||
brain small vessel disease | FGA* | Fga | Alliance of Genome Resources | ||||
brain small vessel disease | FGG* | Fgg | 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 | ||||
carotid artery disease | GSTP1* | Gstp1, Gstp2, Gstp3, Gstp-ps | Alliance of Genome Resources | ||||
carotid artery disease | XDH* | Xdh | Alliance of Genome Resources | ||||
carotid artery disease | UCP2* | Ucp2 | Alliance of Genome Resources | ||||
carotid artery disease | TLR4* | Tlr4 | Alliance of Genome Resources | ||||
carotid artery disease | SREBF2* | Srebf2 | Alliance of Genome Resources | ||||
carotid artery disease | SOD2* | Sod2 | Alliance of Genome Resources | ||||
carotid artery disease | SELPLG* | Selplg | Alliance of Genome Resources | ||||
carotid artery disease | PTGDS* | Ptgds | Alliance of Genome Resources | ||||
carotid artery disease | PRL* | Prl | Alliance of Genome Resources | ||||
carotid artery disease | PPARG* | Pparg | Alliance of Genome Resources | ||||
carotid artery disease | MMP9* | Mmp9 | Alliance of Genome Resources | ||||
carotid artery disease | MMP8* | Mmp8 | Alliance of Genome Resources | ||||
carotid artery disease | MMP2* | Mmp2 | Alliance of Genome Resources | ||||
carotid artery disease | MMP1* | Mmp1a, Mmp1b | Alliance of Genome Resources | ||||
carotid artery disease | LUM* | Lum | Alliance of Genome Resources | ||||
carotid artery disease | AGT* | Agt | Alliance of Genome Resources | ||||
carotid artery disease | AGTR1* | Agtr1a, Agtr1b | Alliance of Genome Resources | ||||
carotid artery disease | CD14* | Cd14 | Alliance of Genome Resources | ||||
carotid artery disease | CETP* | ||||||
carotid artery disease | FGB* | Fgb | Alliance of Genome Resources | ||||
carotid artery disease | GNB3* | Gnb3 | Alliance of Genome Resources | ||||
carotid artery disease | LTA* | Lta | Alliance of Genome Resources | ||||
carotid artery thrombosis | THBD* | Thbd | Alliance of Genome Resources | ||||
carotid stenosis | F2* | F2 | Alliance of Genome Resources | ||||
carotid stenosis | MMP3* | Mmp3 | Alliance of Genome Resources | ||||
carotid stenosis | MTHFR* | Mthfr | Alliance of Genome Resources | ||||
carotid stenosis | MT2A*, MT1A, MT1B, MT1E, MT1F, MT1G, MT1H, MT1L, MT1M, MT1X | Mt1, Mt2 | Alliance of Genome Resources | ||||
carotid stenosis | PTGIS* | Ptgis | Alliance of Genome Resources | ||||
carotid stenosis | FABP2* | Fabp2 | Alliance of Genome Resources | ||||
carotid stenosis | MMP1* | Mmp1a, Mmp1b | Alliance of Genome Resources | ||||
cerebellar ataxia | ATCAY* | Atcay | Alliance of Genome Resources | ||||
cerebellar ataxia | SYNE1* | Syne1 | Alliance of Genome Resources | ||||
cerebellar ataxia | RPGRIP1L* | Rpgrip1l | Alliance of Genome Resources | ||||
cerebellar ataxia | POLG* | Polg | Alliance of Genome Resources | ||||
cerebellar ataxia | L2HGDH* | L2hgdh | 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 | PIK3CA* | Pik3ca | Alliance of Genome Resources | ||||
cerebral cavernous malformation | PON1* | Pon1 | Alliance of Genome Resources | ||||
cerebral cavernous malformation 1 | KRIT1* | Krit1 | Alliance of Genome Resources | ||||
cerebral cavernous malformation 1 | PTGIS* | Ptgis | Alliance of Genome Resources | ||||
cerebral infarction | PDX1* | Pdx1 | Alliance of Genome Resources | ||||
cerebral infarction | PARK7* | Park7 | Alliance of Genome Resources | ||||
cerebral infarction | NR1H3* | Nr1h3 | Alliance of Genome Resources | ||||
cerebral infarction | MYRF* | Myrf | Alliance of Genome Resources | ||||
cerebral infarction | MTR* | Mtr | Alliance of Genome Resources | ||||
cerebral infarction | MTHFR* | Mthfr | Alliance of Genome Resources | ||||
cerebral infarction | LTA* | Lta | Alliance of Genome Resources | ||||
cerebral infarction | LIPG* | Lipg | Alliance of Genome Resources | ||||
cerebral infarction | KCNN4* | Kcnn4 | Alliance of Genome Resources | ||||
cerebral infarction | KALRN* | Kalrn | Alliance of Genome Resources | ||||
cerebral infarction | ITGA9* | Itga9 | Alliance of Genome Resources | ||||
cerebral infarction | IFNB1* | Ifnb1 | Alliance of Genome Resources | ||||
cerebral infarction | HNF1A* | Hnf1a | Alliance of Genome Resources | ||||
cerebral infarction | H19* | ||||||
cerebral infarction | HLA-DRB1*, HLA-DRB3, HLA-DRB4, HLA-DRB5 | H2-Eb1, H2-Eb2 | Alliance of Genome Resources | ||||
cerebral infarction | HLA-A*, HLA-B*, HLA-C, HLA-E, HLA-F, HLA-G, HLA-H | H2-D1, H2-K1, H2-L, H2-M1, H2-M2, H2-M3, H2-M5, H2-M9, H2-M10.1, H2-M10.2, H2-M10.3, H2-M10.4, H2-M10.5, H2-M10.6, H2-M11, H2-Q1, H2-Q2, H2-Q4, H2-Q6, H2-Q7, H2-Q8, H2-Q10, H2-T3, H2-T10, H2-T22, H2-T23 | Alliance of Genome Resources | ||||
cerebral infarction | GRIN1* | Grin1 | Alliance of Genome Resources | ||||
cerebral infarction | PON2* | Pon2 | Alliance of Genome Resources | ||||
cerebral infarction | PRKCH* | Prkch | Alliance of Genome Resources | ||||
cerebral infarction | GPX3* | Gpx3 | Alliance of Genome Resources | ||||
cerebral infarction | GCH1* | Gch1 | Alliance of Genome Resources | ||||
cerebral infarction | FOLH1*, FOLH1B | Folh1 | Alliance of Genome Resources | ||||
cerebral infarction | F7* | F7 | Alliance of Genome Resources | ||||
cerebral infarction | PROS1* | Pros1 | Alliance of Genome Resources | ||||
cerebral infarction | F5* | F5 | Alliance of Genome Resources | ||||
cerebral infarction | F2* | F2 | Alliance of Genome Resources | ||||
cerebral infarction | PTGIS* | Ptgis | Alliance of Genome Resources | ||||
cerebral infarction | SERPING1* | Serping1 | Alliance of Genome Resources | ||||
cerebral infarction | TBXAS1* | Tbxas1 | Alliance of Genome Resources | ||||
cerebral infarction | THBD* | Thbd | Alliance of Genome Resources | ||||
cerebral infarction | ACE* | Ace | Alliance of Genome Resources | ||||
cerebral infarction | AGXT2* | Agxt2 | Alliance of Genome Resources | ||||
cerebral infarction | ALOX5AP* | Alox5ap | Alliance of Genome Resources | ||||
cerebral infarction | TNF* | Tnf | Alliance of Genome Resources | ||||
cerebral infarction | TOMM40* | Tomm40 | Alliance of Genome Resources | ||||
cerebral infarction | TYMS* | Tyms | Alliance of Genome Resources | ||||
cerebral infarction | PON1* | Pon1 | Alliance of Genome Resources | ||||
cerebral infarction | BHMT* | Bhmt, Bhmt1b | Alliance of Genome Resources | ||||
cerebral infarction | APOE* | Apoe | Alliance of Genome Resources | ||||
cerebral infarction | APOA5* | Apoa5 | Alliance of Genome Resources | ||||
cerebral infarction | CBS* | Cbs | Alliance of Genome Resources | ||||
cerebral infarction | PHACTR1* | Phactr1 | Alliance of Genome Resources | ||||
cerebral palsy | ALOX5AP* | Alox5ap | Alliance of Genome Resources | ||||
cerebrovascular disease | GLCE* | Glce | Alliance of Genome Resources | ||||
cerebrovascular disease | G6PD* | G6pd2, G6pdx | Alliance of Genome Resources | ||||
cerebrovascular disease | LMNA* | Lmna | Alliance of Genome Resources | ||||
cerebrovascular disease | NR1H3* | Nr1h3 | Alliance of Genome Resources | ||||
cerebrovascular disease | APOE* | Apoe | Alliance of Genome Resources | ||||
cerebrovascular disease | AGTR1* | Agtr1a, Agtr1b | Alliance of Genome Resources | ||||
cerebrovascular disease | AGT* | Agt | Alliance of Genome Resources | ||||
cerebrovascular disease | P2RY12* | P2ry12 | Alliance of Genome Resources | ||||
cerebrovascular disease | SELE* | Sele | Alliance of Genome Resources | ||||
cervical dystonia | HLA-DQB1*, HLA-DQB2 | H2-Ab1 | Alliance of Genome Resources | ||||
childhood absence epilepsy | CACNA1H* | Cacna1h | Alliance of Genome Resources | ||||
childhood absence epilepsy | SLC2A1* | Slc2a1 | Alliance of Genome Resources | ||||
childhood absence epilepsy | NPY* | Npy | Alliance of Genome Resources | ||||
childhood absence epilepsy | LGI4* | Lgi4 | Alliance of Genome Resources | ||||
childhood absence epilepsy | GRIK1* | Grik1 | Alliance of Genome Resources | ||||
childhood absence epilepsy | GABRG2* | Gabrg2 | Alliance of Genome Resources | ||||
childhood absence epilepsy | GABRB3* | Gabrb3 | Alliance of Genome Resources | ||||
childhood absence epilepsy | CACNG3* | Cacng3 | Alliance of Genome Resources | ||||
childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | MECR* | Mecr | Alliance of Genome Resources | ||||
chordoid glioma | PRKCA* | Prkca | Alliance of Genome Resources | ||||
choreatic disease | HLA-DRB1*, HLA-DRB3, HLA-DRB4, HLA-DRB5 | H2-Eb1, H2-Eb2 | Alliance of Genome Resources | ||||
choreatic disease | VPS13A* | Vps13a | Alliance of Genome Resources | ||||
choreatic disease | HLA-DQA1*, HLA-DQA2 | H2-Aa | Alliance of Genome Resources | ||||
choreatic disease | NKX2-1* | Nkx2-1 | Alliance of Genome Resources | ||||
choreatic disease | HLA-DQB1*, HLA-DQB2 | H2-Ab1 | Alliance of Genome Resources | ||||
classic dopamine transporter deficiency syndrome | SLC6A3* | Slc6a3 | Alliance of Genome Resources | ||||
complex cortical dysplasia with other brain malformations | KIF26A* | Kif26a | Alliance of Genome Resources | ||||
complex cortical dysplasia with other brain malformations | CTNNA2* | Ctnna2 | Alliance of Genome Resources | ||||
complex cortical dysplasia with other brain malformations | CAMSAP1* | Camsap1 | Alliance of Genome Resources | ||||
complex cortical dysplasia with other brain malformations | APC2* | Apc2 | 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 5 | TUBB2A* | Tubb2a | Alliance of Genome Resources | ||||
complex cortical dysplasia with other brain malformations 6 | TUBB* | Tubb5 | Alliance of Genome Resources | ||||
congenital mirror movement disorder | DNAL4* | Dnal4 | Alliance of Genome Resources | ||||
congenital mirror movement disorder | RAD51* | Rad51 | Alliance of Genome Resources | ||||
congenital mirror movement disorder | DCC* | Dcc | Alliance of Genome Resources | ||||
congenital mirror movement disorder | NTN1* | Ntn1 | Alliance of Genome Resources | ||||
Creutzfeldt-Jakob disease | STX1A* | Stx1a | Alliance of Genome Resources | ||||
Creutzfeldt-Jakob disease | HLA-DQB1*, HLA-DQB2 | H2-Ab1 | Alliance of Genome Resources | ||||
cystic echinococcosis | HLA-DRB1*, HLA-DRB3, HLA-DRB4, HLA-DRB5 | H2-Eb1, H2-Eb2 | Alliance of Genome Resources | ||||
cystic echinococcosis | HLA-DQB1*, HLA-DQB2 | H2-Ab1 | Alliance of Genome Resources | ||||
cystic echinococcosis | TLR2* | Tlr2 | Alliance of Genome Resources | ||||
dentatorubral-pallidoluysian atrophy | ATN1* | Atn1 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy | SV2A* | Sv2a | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy | SNF8* | Snf8 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy | SLC32A1* | Slc32a1 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy | DEPDC5* | Depdc5 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy | KCNH5* | Kcnh5 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 1 | ARX* | Arx | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 100 | FBXO28* | Fbxo28 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 101 | GRIN1* | Grin1 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 102 | SLC38A3* | Slc38a3 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 103 | KCNC2* | Kcnc2 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 104 | ATP6V0A1* | Atp6v0a1 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 105 | HID1* | Hid1 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 106 | UFSP2* | Ufsp2 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 107 | NAPB* | Napb | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 108 | MAST3* | Mast3 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 109 | FZR1* | Fzr1 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 11 | SCN2A* | Scn2a | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 110 | CACNA2D1* | Cacna2d1 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 116 | GLUL* | Glul | 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 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* | Aars1 | 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 31A | DNM1* | Dnm1 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 31B | 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 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 64 | RHOBTB2* | Rhobtb2 | 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 6B | SCN1A* | Scn1a | 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 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 85 | SMC1A* | Smc1a | 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 90 | FGF13* | Fgf13 | 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 | ||||
developmental and epileptic encephalopathy 94 | CHD2* | Chd2 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 95 | PIGS* | Pigs | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 96 | NSF* | Nsf | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 97 | CELF2* | Celf2 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 98 | ATP1A2* | Atp1a2 | Alliance of Genome Resources | ||||
developmental and epileptic encephalopathy 99 | ATP1A3* | Atp1a3 | Alliance of Genome Resources | ||||
dopa-responsive dystonia | GCH1* | Gch1 | Alliance of Genome Resources | ||||
dystonia | GCH1* | Gch1 | Alliance of Genome Resources | ||||
dystonia | SPR* | Spr | Alliance of Genome Resources | ||||
dystonia | TIMM8A* | Timm8a1 | Alliance of Genome Resources | ||||
dystonia 12 | ATP1A3* | Atp1a3 | Alliance of Genome Resources | ||||
dystonia 12 | PLA2G6* | Pla2g6 | Alliance of Genome Resources | ||||
dystonia 16 | PRKRA* | Prkra | Alliance of Genome Resources | ||||
dystonia 22, adult-onset | TSPOAP1* | Tspoap1 | Alliance of Genome Resources | ||||
dystonia 22, juvenile-onset | TSPOAP1* | Tspoap1 | 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 28, childhood-onset | KMT2B* | Kmt2b | Alliance of Genome Resources | ||||
dystonia 30 | VPS16* | Vps16 | Alliance of Genome Resources | ||||
dystonia 31 | AOPEP* | Aopep | Alliance of Genome Resources | ||||
dystonia 32 | VPS11* | Vps11 | Alliance of Genome Resources | ||||
dystonia 33 | EIF2AK2* | Eif2ak2 | Alliance of Genome Resources | ||||
dystonia 35, childhood-onset | SHQ1* | Shq1 | Alliance of Genome Resources | ||||
dystonia 37, early-onset with striatal lesions | NUP54* | Nup54 | Alliance of Genome Resources | ||||
dystonia 9 | SLC2A1* | Slc2a1 | Alliance of Genome Resources | ||||
early-onset dystonia and/or spastic paraplegia | ATP5MC3* | Atp5mc3 | Alliance of Genome Resources | ||||
early-onset epilepsy 2 | SETD1A* | Setd1a | Alliance of Genome Resources | ||||
early-onset epilepsy 3 | ATP6V0C* | Atp6v0c | Alliance of Genome Resources | ||||
early-onset vitamin B6-dependent epilepsy 1 | PLPBP* | Plpbp | Alliance of Genome Resources | ||||
early-onset vitamin B6-dependent epilepsy 4 | ALDH7A1* | Aldh7a1 | Alliance of Genome Resources | ||||
epilepsy | ABCB1* | Abcb1a, Abcb1b | Alliance of Genome Resources | ||||
epilepsy | ACHE* | Ache | Alliance of Genome Resources | ||||
epilepsy | ATP1A3* | Atp1a3 | Alliance of Genome Resources | ||||
epilepsy | BCHE* | Bche | Alliance of Genome Resources | ||||
epilepsy | CP* | Cp | Alliance of Genome Resources | ||||
epilepsy | GDNF* | Gdnf | Alliance of Genome Resources | ||||
epilepsy | GRIA1* | Gria1 | Alliance of Genome Resources | ||||
epilepsy | KCNB1* | Kcnb1 | Alliance of Genome Resources | ||||
epilepsy | POLG* | Polg | Alliance of Genome Resources | ||||
epilepsy | TBX1* | Tbx1 | Alliance of Genome Resources | ||||
episodic kinesigenic dyskinesia 3 | TMEM151A* | Tmem151a | Alliance of Genome Resources | ||||
essential tremor | HNMT* | Hnmt | Alliance of Genome Resources | ||||
essential tremor | DRD3* | Drd3 | 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 | ||||
essential tremor 6 | NOTCH2NLC* | ||||||
extrapyramidal and movement disease | CYP2D6*, CYP2D7 | Cyp2d9, Cyp2d10, Cyp2d11, Cyp2d12, Cyp2d22, Cyp2d26, Cyp2d34, Cyp2d40 | 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 focal epilepsy with variable foci 1 | DEPDC5* | Depdc5 | Alliance of Genome Resources | ||||
familial focal epilepsy with variable foci 2 | NPRL2* | Nprl2 | Alliance of Genome Resources | ||||
familial focal epilepsy with variable foci 3 | NPRL3* | Nprl3 | Alliance of Genome Resources | ||||
familial focal epilepsy with variable foci 4 | SCN3A* | Scn3a | 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 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 | ||||
fatal familial insomnia | MIR146A* | Mir146 | Alliance of Genome Resources | ||||
Friedreich ataxia | ND1* | mt-Nd1 | Alliance of Genome Resources | ||||
Friedreich ataxia | AGTR1* | Agtr1a, Agtr1b | Alliance of Genome Resources | ||||
Friedreich ataxia 1 | FXN* | Fxn | Alliance of Genome Resources | ||||
frontotemporal dementia | GRN* | Grn | Alliance of Genome Resources | ||||
frontotemporal dementia | PSEN1* | Psen1 | Alliance of Genome Resources | ||||
frontotemporal dementia | MOBP* | Mobp | Alliance of Genome Resources | ||||
frontotemporal dementia | MAPT* | Mapt | Alliance of Genome Resources | ||||
frontotemporal dementia and/or amyotrophic lateral sclerosis 7 | CHMP2B* | Chmp2b | Alliance of Genome Resources | ||||
generalized epilepsy with febrile seizures plus | SLC32A1* | Slc32a1 | 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 | ||||
glucose transporter type 1 deficiency syndrome 2 | SLC2A1* | Slc2a1 | Alliance of Genome Resources | ||||
Huntington's disease-like 1 | PRNP* | Prnp | Alliance of Genome Resources | ||||
hydrocephalus | CCDC88C* | Ccdc88c | Alliance of Genome Resources | ||||
hydrocephalus | L1CAM* | L1cam | Alliance of Genome Resources | ||||
hydrocephalus | MPDZ* | Mpdz | Alliance of Genome Resources | ||||
hydrocephalus | SMARCC1* | Smarcc1 | Alliance of Genome Resources | ||||
hydrocephalus | WDR81* | Wdr81 | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy | POLR1A* | Polr1a | 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 15 | EPRS1* | Eprs1 | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 16 | TMEM106B* | Tmem106b | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 17 | AIMP2* | Aimp2 | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 18 | DEGS1* | Degs1, Degs1l | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 19 | TMEM63A* | Tmem63a | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 20 | CNP* | Cnp | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 21 | POLR3K* | Polr3k | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 22 | CLDN11* | Cldn11 | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 23 | RNF220* | Rnf220 | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 24 | ATP11A* | Atp11a | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 25 | TMEM163* | Tmem163 | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 26 | SLC35B2* | Slc35b2 | 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 | HYCC1* | Hycc1 | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 7 | POLR3A* | Polr3a | 2 "NOT" models | Alliance of Genome Resources | |||
hypomyelinating leukodystrophy 8 | POLR3B* | Polr3b | Alliance of Genome Resources | ||||
hypomyelinating leukodystrophy 9 | RARS1* | Rars1 | Alliance of Genome Resources | ||||
idiopathic generalized epilepsy | KCNMA1* | Kcnma1 | Alliance of Genome Resources | ||||
idiopathic generalized epilepsy | HCN4* | Hcn4 | 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 | ||||
infantile parkinsonism-dystonia 2 | SLC18A2* | Slc18a2 | Alliance of Genome Resources | ||||
intracranial aneurysm | IL6* | Il6 | Alliance of Genome Resources | ||||
intracranial aneurysm | ENG* | Eng | Alliance of Genome Resources | ||||
intracranial aneurysm | COL22A1* | Col22a1 | Alliance of Genome Resources | ||||
intracranial aneurysm | COL1A2* | Col1a2 | Alliance of Genome Resources | ||||
intracranial aneurysm | BCL2* | Bcl2 | Alliance of Genome Resources | ||||
intracranial aneurysm | MMP9* | Mmp9 | Alliance of Genome Resources | ||||
intracranial aneurysm | PKD1* | Pkd1 | Alliance of Genome Resources | ||||
intracranial aneurysm | PKD2* | Pkd2 | Alliance of Genome Resources | ||||
intracranial aneurysm | SOX17* | Sox17 | Alliance of Genome Resources | ||||
intracranial aneurysm | VCAN* | Vcan | Alliance of Genome Resources | ||||
intracranial aneurysm | KMT2D* | Kmt2d | Alliance of Genome Resources | ||||
intracranial aneurysm | MMP2* | Mmp2 | Alliance of Genome Resources | ||||
intracranial berry aneurysm 12 | THSD1* | Thsd1 | Alliance of Genome Resources | ||||
intracranial embolism | KL* | Kl | Alliance of Genome Resources | ||||
intracranial vasospasm | HMOX1* | Hmox1 | Alliance of Genome Resources | ||||
intracranial vasospasm | RYR1* | Ryr1 | Alliance of Genome Resources | ||||
Joubert syndrome | FAM149B1* | Fam149b | Alliance of Genome Resources | ||||
Joubert syndrome | TMEM216* | Tmem216 | Alliance of Genome Resources | ||||
Joubert syndrome | TOGARAM1* | Togaram1 | Alliance of Genome Resources | ||||
Joubert syndrome | TMEM237* | Tmem237 | Alliance of Genome Resources | ||||
Joubert syndrome | INPP5E* | Inpp5e | Alliance of Genome Resources | ||||
Joubert syndrome | IFT74* | Ift74 | Alliance of Genome Resources | ||||
Joubert syndrome | TMEM218* | Tmem218 | Alliance of Genome Resources | ||||
Joubert syndrome | KIAA0753* | 4933427D14Rik | Alliance of Genome Resources | ||||
Joubert syndrome | ARL3* | Arl3 | Alliance of Genome Resources | ||||
Joubert syndrome | B9D2* | B9d2 | 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 4 | NPHP4* | Nphp4 | Alliance of Genome Resources | ||||
Joubert syndrome 4 | AHI1* | Ahi1 | 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 | BRD2* | Brd2 | Alliance of Genome Resources | ||||
juvenile myoclonic epilepsy 10 | CILK1* | Cilk1 | Alliance of Genome Resources | ||||
kuru | PRNP* | Prnp | Alliance of Genome Resources | ||||
leukodystrophy | AARS1* | Aars1 | Alliance of Genome Resources | ||||
leukoencephalopathy with vanishing white matter | EIF2B2* | Eif2b2 | Alliance of Genome Resources | ||||
leukoencephalopathy with vanishing white matter 1 | EIF2B1* | Eif2b1 | Alliance of Genome Resources | ||||
leukoencephalopathy with vanishing white matter 2 | EIF2B2* | Eif2b2 | Alliance of Genome Resources | ||||
leukoencephalopathy with vanishing white matter 3 | EIF2B3* | Eif2b3 | Alliance of Genome Resources | ||||
leukoencephalopathy with vanishing white matter 4 | EIF2B4* | Eif2b4 | Alliance of Genome Resources | ||||
leukoencephalopathy with vanishing white matter 5 | EIF2B5* | Eif2b5 | Alliance of Genome Resources | ||||
Machado-Joseph disease | BECN1* | Becn1 | Alliance of Genome Resources | ||||
Machado-Joseph disease | ATXN3* | Atxn3 | 1 model | Alliance of Genome Resources | |||
medulloblastoma | ELP1* | Elp1 | Alliance of Genome Resources | ||||
medulloblastoma | APC* | Apc | Alliance of Genome Resources | ||||
medulloblastoma | CTNNB1* | Ctnnb1 | Alliance of Genome Resources | ||||
medulloblastoma | PTCH2* | Ptch2 | 2 models | Alliance of Genome Resources | |||
medulloblastoma | GSTT1* | Gstt1 | Alliance of Genome Resources | ||||
medulloblastoma | GSTM1*, GSTM5 | Gstm1, Gstm2, Gstm3, Gstm6 | Alliance of Genome Resources | ||||
medulloblastoma | BRCA2* | Brca2 | 2 models | Alliance of Genome Resources | |||
medulloblastoma | GPR161* | Gpr161 | Alliance of Genome Resources | ||||
medulloblastoma | TSC2* | Tsc2 | Alliance of Genome Resources | ||||
medulloblastoma | SUFU* | Sufu | 1 model | Alliance of Genome Resources | |||
megalencephalic leukoencephalopathy with subcortical cysts | GPRC5B* | Gprc5b | Alliance of Genome Resources | ||||
megalencephalic leukoencephalopathy with subcortical cysts | AQP4* | Aqp4 | 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 | ||||
middle cerebral artery infarction | ALB* | Alb | Alliance of Genome Resources | ||||
middle cerebral artery infarction | SHH* | Shh | Alliance of Genome Resources | ||||
middle cerebral artery infarction | PARK7* | Park7 | Alliance of Genome Resources | ||||
middle cerebral artery infarction | NRG1* | Nrg1 | Alliance of Genome Resources | ||||
middle cerebral artery infarction | NCAM1* | Ncam1 | Alliance of Genome Resources | ||||
middle cerebral artery infarction | IL1RN* | Il1rn | Alliance of Genome Resources | ||||
middle cerebral artery infarction | HMOX1* | Hmox1 | Alliance of Genome Resources | ||||
middle cerebral artery infarction | F12* | F12 | Alliance of Genome Resources | ||||
middle cerebral artery infarction | EPO* | Epo | Alliance of Genome Resources | ||||
middle cerebral artery infarction | CXCL10* | Cxcl10 | Alliance of Genome Resources | ||||
middle cerebral artery infarction | CSF3* | Csf3 | Alliance of Genome Resources | ||||
middle cerebral artery infarction | CRP* | Crp | Alliance of Genome Resources | ||||
migraine | TNF* | Tnf | Alliance of Genome Resources | ||||
migraine | PHACTR1* | Phactr1 | Alliance of Genome Resources | ||||
migraine | NOS3* | Nos3 | Alliance of Genome Resources | ||||
migraine | TRPV1* | Trpv1 | Alliance of Genome Resources | ||||
migraine | MTHFR* | Mthfr | Alliance of Genome Resources | ||||
migraine | KCNK18* | Kcnk18 | Alliance of Genome Resources | ||||
migraine | ESR1* | Esr1 | Alliance of Genome Resources | ||||
migraine | EDNRA* | Ednra | Alliance of Genome Resources | ||||
migraine | CALCA*, CALCB | Calca, Calcb | Alliance of Genome Resources | ||||
migraine | CACNA1A* | Cacna1a | Alliance of Genome Resources | ||||
migraine with aura | ATP1A2* | Atp1a2 | Alliance of Genome Resources | ||||
migraine with aura | TRPV3* | Trpv3 | Alliance of Genome Resources | ||||
migraine with aura | MTHFR* | Mthfr | Alliance of Genome Resources | ||||
migraine with aura | DRD2* | Drd2 | Alliance of Genome Resources | ||||
migraine with aura | DBH* | Dbh | Alliance of Genome Resources | ||||
migraine with aura | CACNA1A* | Cacna1a | Alliance of Genome Resources | ||||
migraine without aura | LDLR* | Ldlr | Alliance of Genome Resources | ||||
migraine without aura | TNF* | Tnf | Alliance of Genome Resources | ||||
movement disease | DRD2* | Drd2 | Alliance of Genome Resources | ||||
movement disease | GSTP1* | Gstp1, Gstp2, Gstp3, Gstp-ps | Alliance of Genome Resources | ||||
movement disease | GSTM1*, GSTM5 | Gstm1, Gstm2, Gstm3, Gstm6 | Alliance of Genome Resources | ||||
Moyamoya disease | ACTA2* | Acta2 | Alliance of Genome Resources | ||||
Moyamoya disease | PHACTR1* | Phactr1 | Alliance of Genome Resources | ||||
Moyamoya disease | RNF213* | Rnf213 | 1 "NOT" model | Alliance of Genome Resources | |||
Moyamoya disease | TIMP2* | Timp2 | Alliance of Genome Resources | ||||
Moyamoya disease | ANO1* | Ano1 | Alliance of Genome Resources | ||||
Moyamoya disease | GUCY1A1* | Gucy1a1 | Alliance of Genome Resources | ||||
Moyamoya disease | HLA-A*, HLA-B, HLA-C, HLA-E, HLA-F, HLA-G, HLA-H | H2-D1, H2-K1, H2-L, H2-M1, H2-M2, H2-M3, H2-M5, H2-M9, H2-M10.1, H2-M10.2, H2-M10.3, H2-M10.4, H2-M10.5, H2-M10.6, H2-M11, H2-Q1, H2-Q2, H2-Q4, H2-Q6, H2-Q7, H2-Q8, H2-Q10, H2-T3, H2-T10, H2-T22, H2-T23 | Alliance of Genome Resources | ||||
myoclonic-atonic epilepsy | SLC6A1* | Slc6a1 | Alliance of Genome Resources | ||||
myoclonic-atonic epilepsy | TBC1D24* | Tbc1d24 | Alliance of Genome Resources | ||||
myoclonic dystonia 26 | KCTD17* | Kctd17 | Alliance of Genome Resources | ||||
myoclonic dystonia 34 | KCNN2* | Kcnn2 | Alliance of Genome Resources | ||||
neuroaxonal dystrophy | PLA2G6* | Pla2g6 | Alliance of Genome Resources | ||||
neuroaxonal dystrophy | NAGA* | Naga | Alliance of Genome Resources | ||||
nonprogressive cerebellar ataxia with mental retardation | CAMTA1* | Camta1 | Alliance of Genome Resources | ||||
optic nerve glioma | NF1* | Nf1 | Alliance of Genome Resources | ||||
Parkinsonism | HSPA1A*, HSPA1B | Hspa1a, Hspa1b | Alliance of Genome Resources | ||||
Parkinsonism | GBA1* | Gba1 | Alliance of Genome Resources | ||||
Parkinsonism | GCH1* | Gch1 | Alliance of Genome Resources | ||||
Parkinsonism | GDNF* | Gdnf | Alliance of Genome Resources | ||||
Parkinsonism | PARK7* | Park7 | Alliance of Genome Resources | ||||
Parkinsonism | MANF* | Manf | Alliance of Genome Resources | ||||
Parkinsonism | LRRK2* | Lrrk2 | Alliance of Genome Resources | ||||
Parkinsonism | FGF2* | Fgf2 | Alliance of Genome Resources | ||||
Parkinsonism | BDNF* | Bdnf | Alliance of Genome Resources | ||||
Parkinsonism | TNFRSF1B* | Tnfrsf1b | Alliance of Genome Resources | ||||
Parkinsonism | TH* | Th | Alliance of Genome Resources | ||||
paroxysmal nonkinesigenic dyskinesia 3 | KCNMA1* | Kcnma1 | Alliance of Genome Resources | ||||
PEHO syndrome | ZNHIT3* | Znhit3 | Alliance of Genome Resources | ||||
Pick's disease | PSEN1* | Psen1 | Alliance of Genome Resources | ||||
Pick's disease | MAP2K6* | Map2k6 | Alliance of Genome Resources | ||||
Pick's disease | MAPT* | Mapt | Alliance of Genome Resources | ||||
pleomorphic xanthoastrocytoma | BRAF* | Braf | Alliance of Genome Resources | ||||
polymicrogyria | WDR62* | Wdr62 | Alliance of Genome Resources | ||||
porencephaly | COL4A2* | Col4a2 | Alliance of Genome Resources | ||||
prion disease | SOD1* | Sod1 | Alliance of Genome Resources | ||||
progressive leukoencephalopathy with ovarian failure | AARS2* | Aars2 | Alliance of Genome Resources | ||||
progressive myoclonus epilepsy | SLC7A6OS* | Slc7a6os | Alliance of Genome Resources | ||||
progressive myoclonus epilepsy | SEMA6B* | Sema6b | Alliance of Genome Resources | ||||
progressive myoclonus epilepsy | EPM2A* | Epm2a | 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 | NAT2*, NAT1 | Nat1, Nat2, Nat3 | Alliance of Genome Resources | ||||
progressive supranuclear palsy | MAP2K6* | Map2k6 | 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 quadriplegic cerebral palsy 2 | KANK1* | Kank1 | Alliance of Genome Resources | ||||
spastic quadriplegic cerebral palsy 3 | ADD3* | Add3 | 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 | ||||
status epilepticus | BDNF* | Bdnf | Alliance of Genome Resources | ||||
Stiff-Person syndrome | HSD17B4* | Hsd17b4 | Alliance of Genome Resources | ||||
temporal lobe epilepsy | MAPT* | Mapt | Alliance of Genome Resources | ||||
temporal lobe epilepsy | NPY* | Npy | Alliance of Genome Resources | ||||
temporal lobe epilepsy | AQP4* | Aqp4 | Alliance of Genome Resources | ||||
temporal lobe epilepsy | PDYN* | Pdyn | Alliance of Genome Resources | ||||
temporal lobe epilepsy | KCNAB1* | Kcnab1 | Alliance of Genome Resources | ||||
torsion dystonia 2 | HPCA* | Hpca | Alliance of Genome Resources | ||||
torsion dystonia 4 | TUBB4A* | Tubb4a | Alliance of Genome Resources | ||||
transient cerebral ischemia | ERCC1* | Ercc1 | Alliance of Genome Resources | ||||
transient cerebral ischemia | BCL2L2*, BCL2L2-PABPN1 | Bcl2l2 | Alliance of Genome Resources | ||||
transient cerebral ischemia | CSF3* | Csf3 | Alliance of Genome Resources | ||||
transient cerebral ischemia | EPO* | Epo | Alliance of Genome Resources | ||||
transient cerebral ischemia | F12* | F12 | Alliance of Genome Resources | ||||
transient cerebral ischemia | GOT1* | Got1 | Alliance of Genome Resources | ||||
transient cerebral ischemia | IL1RN* | Il1rn | Alliance of Genome Resources | ||||
transient cerebral ischemia | NAMPT* | Nampt | Alliance of Genome Resources | ||||
transient cerebral ischemia | NRG1* | Nrg1 | Alliance of Genome Resources | ||||
transient cerebral ischemia | SERPINF1* | Serpinf1 | Alliance of Genome Resources | ||||
transient cerebral ischemia | SOD1* | Sod1 | Alliance of Genome Resources | ||||
transient cerebral ischemia | TFPI* | Tfpi | Alliance of Genome Resources | ||||
traumatic brain injury | APP* | App | Alliance of Genome Resources | ||||
viral encephalitis | CXCL8* | ||||||
visual epilepsy | NPY* | Npy | Alliance of Genome Resources | ||||
visual epilepsy | TBC1D24* | Tbc1d24 | Alliance of Genome Resources | ||||
visual epilepsy | TNF* | Tnf | Alliance of Genome Resources | ||||
visual epilepsy | L2HGDH* | L2hgdh | Alliance of Genome Resources | ||||
visual epilepsy | CNTNAP2* | Cntnap2 | Alliance of Genome Resources | ||||
visual epilepsy | CDKL5* | Cdkl5 | Alliance of Genome Resources | ||||
visual epilepsy | ASPM* | Aspm | Alliance of Genome Resources | ||||
visual epilepsy | FCGR3A*, FCGR3B | Fcgr4 | Alliance of Genome Resources | ||||
visual epilepsy | FCGR2A*, FCGR2B, FCGR2C | Fcgr2b, Fcgr3 | Alliance of Genome Resources | ||||
visual epilepsy | TUBA1A* | Tuba1a | Alliance of Genome Resources | ||||
visual epilepsy | APP* | App | Alliance of Genome Resources | ||||
West syndrome | MC2R* | Mc2r | Alliance of Genome Resources | ||||
West syndrome | STXBP1* | Stxbp1 | 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.
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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(Plp1-Lmnb1)#Yfu | 1 model | |
adult-onset autosomal dominant demyelinating leukodystrophy | Tg(Lmnb1)1Yfu | 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(Eno2-ATN1)3Tx | 1 model | |
dentatorubral-pallidoluysian atrophy | Tg(Prnp-ATN1)150Dbo | 1 model | |
dentatorubral-pallidoluysian atrophy | Tg(ATN1*)Q129Stsu | 1 model | |
dentatorubral-pallidoluysian atrophy | Tg(Eno2-ATN1)14Tx | 1 model | |
dentatorubral-pallidoluysian atrophy | Tg(Prnp-ATN1)124Dbo | 1 model | |
epilepsy | Tg(Camk2a-Bdnf)A9Stl | 1 model | |
epilepsy | Tg(Eno2-Scn2a1*)Q54Mm | 3 models | |
epilepsy | Tg(RP23-65I14)1Jno | 1 model | |
epilepsy | Tg(RP23-65I14)2Jno | 1 model | |
familial temporal lobe epilepsy 1 | Tg(Lgi1*)#Mpan | 1 model | |
frontotemporal dementia | Tg(Prnp-MAPT)7Vle | 1 model | |
frontotemporal dementia | Tg(Thy1-MAPT*P301S)2541Godt | 1 model | |
frontotemporal dementia | Tg(Thy1-MAPT*V337M)1Godt | 1 model | |
frontotemporal dementia | Tg(Thy1-TARDBP)4Singh | 2 models | |
frontotemporal dementia | Tg(Thy1-TARDBP)6Singh | 1 model | |
frontotemporal dementia | Tg(Prnp-MAPT*P301S)50Hiw | 1 model | |
frontotemporal dementia | Tg(Tuba1-MAPT)14Vle | 1 model | |
frontotemporal dementia | Tg(Thy1-MAPT*K369I)K3Gotz | 1 model | |
frontotemporal dementia | Tg(Prnp-MAPT)43Vle | 1 model | |
frontotemporal dementia | Tg(PDGFB-MAPT*V337M)1Atak | 1 model | |
frontotemporal dementia | Tg(Prnp-TARDBP*A315T)95Balo | 1 model | |
frontotemporal dementia | Tg(tetO-CHMP2B*)3Fbga | 1 model | |
frontotemporal dementia | Tg(Prnp-MAPT*R406W)21807Dwst | 1 model | |
frontotemporal dementia | Tg(Thy1-MAPT*)1Avil | 1 model | |
frontotemporal dementia | Tg(Prnp-MAPT*P301L)JNPL3Hlmc | 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)174Sbp | 1 model | |
Gerstmann-Straussler-Scheinker syndrome | Tg(Prnp*P101L)2247Sbp | 1 model | |
Gerstmann-Straussler-Scheinker syndrome | Tg(Prnp*P101L)2862Sbp | 1 model | |
Gerstmann-Straussler-Scheinker syndrome | Tg(Prnp*P101L)2866Sbp | 3 models | |
Gerstmann-Straussler-Scheinker syndrome | Tg(Prnp*A116V*M128V)1309Jama | 1 model | |
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(TARDBP)#Jpj | 1 model | |
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Thy1-TARDBP*)BOddo | 2 models | |
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(Camk2a-Tardbp)#Ckjs | 1 model | |
Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | Tg(TARDBP*A315T)#Jpj | 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*G348C)#Jpj | 1 model | |
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(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 | |
Machado-Joseph disease | Tg(Pcp2-ATXN3*69Q)bHirai | 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 | |
medulloblastoma | Tg(tetO-Ifng)184Pop | 2 models | |
medulloblastoma | Tg(Neurod2-Smo*A1)199Jols | 3 models | |
medulloblastoma | Tg(Neurod2-Smo*A2)#Jols | 1 model | |
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 | Tg(Plp)72Kan | 1 model | |
Pelizaeus-Merzbacher disease | Dp(XTceal3-Plp1)1Gmh | 1 model | |
Pelizaeus-Merzbacher disease | Tg(Plp)66Kan | 2 models | |
Pick's disease | Tg(Thy1-MAPT*L266V*G272V)13Ema | 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*)105Xjl | 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*)71-27Xjl | 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(GFAP-ATXN7*92Q)2542Als | 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)2521Als | 1 model | |
torsion dystonia 1 | Tg(CMV-TOR1A*)2Nush | 1 model | |
torsion dystonia 1 | Tg(Eno2-TOR1A*)13Shas | 1 model | |
torsion dystonia 1 | Tg(CMV-TOR1A*)1Nush | 1 model |