sleep disorder Gene Set

Dataset DISEASES Experimental Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A disease of mental health that involves disruption of sleep patterns. (Human Disease Ontology, DOID_535)
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Genes

14 genes associated with the disease sleep disorder in GWAS datasets from the DISEASES Experimental Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
TRAC T cell receptor alpha constant 1.45684
HLA-DQA2 major histocompatibility complex, class II, DQ alpha 2 0.464771
GRM3 glutamate receptor, metabotropic 3 0.438544
CHKB choline kinase beta 0.429338
OPN3 opsin 3 0.403461
KMO kynurenine 3-monooxygenase (kynurenine 3-hydroxylase) 0.403461
DENND1B DENN/MADD domain containing 1B 0.403461
C1ORF53 chromosome 1 open reading frame 53 0.327313
BTRC beta-transducin repeat containing E3 ubiquitin protein ligase 0.274608
TMEM182 transmembrane protein 182 0.15771
OR6C3 olfactory receptor, family 6, subfamily C, member 3 0.126165
CDH13 cadherin 13 0.064973
PBX3 pre-B-cell leukemia homeobox 3 0.052255
CDH6 cadherin 6, type 2, K-cadherin (fetal kidney) 0.043246