insomnia Gene Set

Dataset	GWASdb SNP-Phenotype Associations
Category	disease or phenotype associations
Type	phenotype
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)
External Link	http://jjwanglab.org/gwasdb/gwasdb2/gwasdb2/go_trait/HP:0100785
Similar Terms
Downloads & Tools

Genes

6 genes associated with the insomnia phenotype in GWAS datasets from the GWASdb SNP-Phenotype Associations dataset.

Symbol	Name	Standardized Value
PRIMA1	proline rich membrane anchor 1	1.04365
SLC2A13	solute carrier family 2 (facilitated glucose transporter), member 13	1.00059
MTUS2	microtubule associated tumor suppressor candidate 2	0.942765
NEDD4L	neural precursor cell expressed, developmentally down-regulated 4-like, E3 ubiquitin protein ligase	0.882984
ADARB2	adenosine deaminase, RNA-specific, B2 (non-functional)	0.445522
KCNMA1	potassium channel, calcium activated large conductance subfamily M alpha, member 1	0.426397