Narcolepsy-Cataplexy Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0751362
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Genes

30 genes associated with the disease Narcolepsy-Cataplexy Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACHE acetylcholinesterase (Yt blood group)
CD59 CD59 molecule, complement regulatory protein
CHAT choline O-acetyltransferase
CHKB choline kinase beta
CPT1B carnitine palmitoyltransferase 1B (muscle)
CTSH cathepsin H
FRS2 fibroblast growth factor receptor substrate 2
GNAO1 guanine nucleotide binding protein (G protein), alpha activating activity polypeptide O
HCRT hypocretin (orexin) neuropeptide precursor
HCRTR1 hypocretin (orexin) receptor 1
HCRTR2 hypocretin (orexin) receptor 2
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
HLA-DQB2 major histocompatibility complex, class II, DQ beta 2
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
LEP leptin
MOG myelin oligodendrocyte glycoprotein
P2RY11 purinergic receptor P2Y, G-protein coupled, 11
PENK proenkephalin
PSG5 pregnancy specific beta-1-glycoprotein 5
REM1 RAS (RAD and GEM)-like GTP-binding 1
SLC18A3 solute carrier family 18 (vesicular acetylcholine transporter), member 3
SLC5A7 solute carrier family 5 (sodium/choline cotransporter), member 7
SNTA1 syntrophin, alpha 1
SOCS2 suppressor of cytokine signaling 2
TAC1 tachykinin, precursor 1
TNFSF4 tumor necrosis factor (ligand) superfamily, member 4
TRA T cell receptor alpha locus
TRH thyrotropin-releasing hormone
UBXN2B UBX domain protein 2B
ZNF365 zinc finger protein 365