Narcolepsy Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A sleep disorder that involves an excessive urge to sleep at inappropriate times, such as while at work. (Human Disease Ontology, DOID_8986)
External Link http://ctdbase.org/detail.go?type=disease&acc=MESH:D009290
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Genes

18 genes/proteins associated with the disease Narcolepsy from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1 2.88009
SOCS2 suppressor of cytokine signaling 2 2.88009
TRA T cell receptor alpha locus 2.88009
TRH thyrotropin-releasing hormone 2.88009
NRCLP4 Narcolepsy 4 2.88009
NRCLP2 Narcolepsy, HLA-associated 2.88009
CPT1B carnitine palmitoyltransferase 1B (muscle) 2.88009
HCRTR2 hypocretin (orexin) receptor 2 2.88009
HLA-DRB1 major histocompatibility complex, class II, DR beta 1 2.88009
NRCLP3 Narcolepsy 3 2.88009
TAC1 tachykinin, precursor 1 2.88009
P2RY11 purinergic receptor P2Y, G-protein coupled, 11 2.88009
CHKB choline kinase beta 2.88009
PENK proenkephalin 2.88009
NRCLP5 Narcolepsy 5 2.88009
SLC6A3 solute carrier family 6 (neurotransmitter transporter), member 3 1.14885
FOS FBJ murine osteosarcoma viral oncogene homolog 1.09998
TH tyrosine hydroxylase 1.02225