agitation Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000713
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Genes

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

Symbol Name
AFF2 AF4/FMR2 family, member 2
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
CECR1 cat eye syndrome chromosome region, candidate 1
GNAS GNAS complex locus
GRN granulin
HSD17B10 hydroxysteroid (17-beta) dehydrogenase 10
IGF1R insulin-like growth factor 1 receptor
PAK3 p21 protein (Cdc42/Rac)-activated kinase 3
PDE11A phosphodiesterase 11A
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
SPAST spastin
SUOX sulfite oxidase