ventricular arrhythmia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004308
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Genes

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

Symbol Name
ACTC1 actin, alpha, cardiac muscle 1
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CAV3 caveolin 3
DPP6 dipeptidyl-peptidase 6
DSC2 desmocollin 2
DSG2 desmoglein 2
DSP desmoplakin
DTNA dystrobrevin, alpha
GAA glucosidase, alpha; acid
GPD1L glycerol-3-phosphate dehydrogenase 1-like
GYG1 glycogenin 1
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
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LAMP2 lysosomal-associated membrane protein 2
LDB3 LIM domain binding 3
LMNA lamin A/C
MTFMT mitochondrial methionyl-tRNA formyltransferase
MYH7 myosin, heavy chain 7, cardiac muscle, beta
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
PKP2 plakophilin 2
PLN phospholamban
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
RAF1 Raf-1 proto-oncogene, serine/threonine kinase
RYR2 ryanodine receptor 2 (cardiac)
SCN1B sodium channel, voltage gated, type I beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SLC25A20 solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
SNTA1 syntrophin, alpha 1
TGFB3 transforming growth factor, beta 3
TMEM43 transmembrane protein 43
TSC1 tuberous sclerosis 1
TSC2 tuberous sclerosis 2