insomnia Gene Set

Dataset	GeneRIF Biological Term Annotations
Category	structural or functional annotations
Type	biological term
Description	Disorders characterized by impairment of the ability to initiate or maintain sleep. This may occur as a primary disorder or in association with another medical or psychiatric condition (Experimental Factor Ontology, EFO_0004698)
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Genes

19 genes co-occuring with the biological term insomnia in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

Symbol	Name
ADORA2A	adenosine A2a receptor
AHR	aryl hydrocarbon receptor
AHRR	aryl-hydrocarbon receptor repressor
APOE	apolipoprotein E
CLOCK	clock circadian regulator
CRP	C-reactive protein, pentraxin-related
GABRB3	gamma-aminobutyric acid (GABA) A receptor, beta 3
GHRL	ghrelin/obestatin prepropeptide
HBA1	hemoglobin, alpha 1
LEP	leptin
MAOA	monoamine oxidase A
MIR182	microRNA 182
MTNR1A	melatonin receptor 1A
OPRM1	opioid receptor, mu 1
PER3	period circadian clock 3
PPARGC1A	peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
PRNP	prion protein
SLC6A4	solute carrier family 6 (neurotransmitter transporter), member 4
TPH1	tryptophan hydroxylase 1