Familial Neurocardiogenic Syncope Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1836438
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Genes

16 genes associated with the disease Familial Neurocardiogenic Syncope in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADM adrenomedullin
ARIH1 ariadne RBR E3 ubiquitin protein ligase 1
AVP arginine vasopressin
CD59 CD59 molecule, complement regulatory protein
EDN1 endothelin 1
GNAS GNAS complex locus
GNG2 guanine nucleotide binding protein (G protein), gamma 2
GPR174 G protein-coupled receptor 174
MBL2 mannose-binding lectin (protein C) 2, soluble
NLRP3 NLR family, pyrin domain containing 3
NOS3 nitric oxide synthase 3 (endothelial cell)
NPY neuropeptide Y
PRKCE protein kinase C, epsilon
SLC6A2 solute carrier family 6 (neurotransmitter transporter), member 2
TNF tumor necrosis factor