restless legs syndrome Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A central nervous system disease characterized by throbbing, pulling creeping or other unpleasant sensations in the legs and the irresistible urge to move them. (Human Disease Ontology, DOID_0050425)
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15 genes associated with the disease restless legs syndrome in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ATXN1 ataxin 1
ATXN2 ataxin 2
ATXN3 ataxin 3
ATXN7 ataxin 7
BTBD9 BTB (POZ) domain containing 9
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
COMT catechol-O-methyltransferase
MAOA monoamine oxidase A
MAOB monoamine oxidase B
MAP2K5 mitogen-activated protein kinase kinase 5
MEIS1 Meis homeobox 1
NOS1 nitric oxide synthase 1 (neuronal)
PTPRD protein tyrosine phosphatase, receptor type, D
SKOR1 SKI family transcriptional corepressor 1
TBP TATA box binding protein