Dystonic Disorders Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

30 genes associated with the Dystonic Disorders phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
ARSG arylsulfatase G
ATP13A2 ATPase type 13A2
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
BDNF brain-derived neurotrophic factor
DRD1 dopamine receptor D1
DRD5 dopamine receptor D5
GABRA1 gamma-aminobutyric acid (GABA) A receptor, alpha 1
GABRB3 gamma-aminobutyric acid (GABA) A receptor, beta 3
GABRG2 gamma-aminobutyric acid (GABA) A receptor, gamma 2
GCH1 GTP cyclohydrolase 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
KLC1 kinesin light chain 1
LRRK2 leucine-rich repeat kinase 2
MR1 major histocompatibility complex, class I-related
NKX2-1 NK2 homeobox 1
PARK2 parkin RBR E3 ubiquitin protein ligase
PCBD1 pterin-4 alpha-carbinolamine dehydratase/dimerization cofactor of hepatocyte nuclear factor 1 alpha
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
PTS 6-pyruvoyltetrahydropterin synthase
QDPR quinoid dihydropteridine reductase
SGCE sarcoglycan, epsilon
SPR sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)
STON2 stonin 2
TAF1 TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
TBP TATA box binding protein
TH tyrosine hydroxylase
THAP1 THAP domain containing, apoptosis associated protein 1
TOR1A torsin family 1, member A (torsin A)
TOR1B torsin family 1, member B (torsin B)