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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Genes

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