ventricular fibrillation Gene Set

Dataset HPO Gene-Disease 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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001663
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Genes

10 genes associated with the ventricular fibrillation phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DPP6 dipeptidyl-peptidase 6
DSP desmoplakin
GPD1L glycerol-3-phosphate dehydrogenase 1-like
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
SCN1B sodium channel, voltage gated, type I beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit