restlessness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000711
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Genes

20 genes associated with the restlessness phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AFF2 AF4/FMR2 family, member 2
AMT aminomethyltransferase
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CECR1 cat eye syndrome chromosome region, candidate 1
CHMP2B charged multivesicular body protein 2B
CLN8 ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation)
GCSH glycine cleavage system protein H (aminomethyl carrier)
GLDC glycine dehydrogenase (decarboxylating)
GNAS GNAS complex locus
GRN granulin
HSD17B10 hydroxysteroid (17-beta) dehydrogenase 10
IGF1R insulin-like growth factor 1 receptor
KDM5C lysine (K)-specific demethylase 5C
PAK3 p21 protein (Cdc42/Rac)-activated kinase 3
PDE11A phosphodiesterase 11A
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PRNP prion protein
SPAST spastin
SUOX sulfite oxidase
TSEN54 TSEN54 tRNA splicing endonuclease subunit