Disorders of Excessive Somnolence Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
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Genes

17 genes associated with the Disorders of Excessive Somnolence phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
APOE apolipoprotein E
CHKB choline kinase beta
CLOCK clock circadian regulator
COMT catechol-O-methyltransferase
CPT1B carnitine palmitoyltransferase 1B (muscle)
CTLA4 cytotoxic T-lymphocyte-associated protein 4
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DRD2 dopamine receptor D2
DRD3 dopamine receptor D3
DRD4 dopamine receptor D4
HCRT hypocretin (orexin) neuropeptide precursor
HCRTR2 hypocretin (orexin) receptor 2
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
MAOA monoamine oxidase A
NPS neuropeptide S
TRIB1 tribbles pseudokinase 1