movement disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
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23 genes involed in the disease movement disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ACTB actin, beta
ANO3 anoctamin 3
ATP1A3 ATPase, Na+/K+ transporting, alpha 3 polypeptide
BCAP31 B-cell receptor-associated protein 31
CIZ1 CDKN1A interacting zinc finger protein 1
DRD2 dopamine receptor D2
DRD5 dopamine receptor D5
GCH1 GTP cyclohydrolase 1
GNAL guanine nucleotide binding protein (G protein), alpha activating activity polypeptide, olfactory type
MAPT microtubule-associated protein tau
PLA2G6 phospholipase A2, group VI (cytosolic, calcium-independent)
PNKD paroxysmal nonkinesigenic dyskinesia
PRKRA protein kinase, interferon-inducible double stranded RNA dependent activator
PRRT2 proline-rich transmembrane protein 2
SGCE sarcoglycan, epsilon
SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3
SLITRK1 SLIT and NTRK-like family, member 1
SPR sepiapterin reductase (7,8-dihydrobiopterin:NADP+ oxidoreductase)
TAF1 TAF1 RNA polymerase II, TATA box binding protein (TBP)-associated factor, 250kDa
TH tyrosine hydroxylase
THAP1 THAP domain containing, apoptosis associated protein 1
TOR1A torsin family 1, member A (torsin A)