drowsiness Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Excessive daytime sleepiness. (Human Phenotype Ontology, HP_0002329)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002329
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Genes

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

Symbol Name
ABCC8 ATP-binding cassette, sub-family C (CFTR/MRP), member 8
ATP1A2 ATPase, Na+/K+ transporting, alpha 2 polypeptide
CACNA1A calcium channel, voltage-dependent, P/Q type, alpha 1A subunit
HCRT hypocretin (orexin) neuropeptide precursor
THRA thyroid hormone receptor, alpha