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* 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.
     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