Ventricular Fibrillation Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Uncontrolled contractions of muscles fibers in the left ventricle not producing contraction of the left ventricle. Ventricular fibrillation usually begins with a ventricular premature contraction and a short run of rapid ventricular tachycardia degenerating into uncoordinating ventricular fibrillations. (Human Phenotype Ontology, HP_0001663)
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Genes

26 genes associated with the Ventricular Fibrillation phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADRB1 adrenoceptor beta 1
ADRB2 adrenoceptor beta 2, surface
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CACNA2D1 calcium channel, voltage-dependent, alpha 2/delta subunit 1
CACNB2 calcium channel, voltage-dependent, beta 2 subunit
CXADR coxsackie virus and adenovirus receptor
DSC2 desmocollin 2
DSG2 desmoglein 2
DSP desmoplakin
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNJ8 potassium channel, inwardly rectifying subfamily J, member 8
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
NRG1 neuregulin 1
PKP2 plakophilin 2
RYR2 ryanodine receptor 2 (cardiac)
SCN10A sodium channel, voltage gated, type X alpha subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SELP selectin P (granule membrane protein 140kDa, antigen CD62)
SELPLG selectin P ligand
SEMA3A sema domain, immunoglobulin domain (Ig), short basic domain, secreted, (semaphorin) 3A
SERPINE1 serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 1
ZFHX3 zinc finger homeobox 3