Ventricular Tachycardia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1631597
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Genes

29 genes associated with the disease Ventricular Tachycardia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
AIP aryl hydrocarbon receptor interacting protein
ANK2 ankyrin 2, neuronal
ASPH aspartate beta-hydroxylase
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
CALM1 calmodulin 1 (phosphorylase kinase, delta)
CALM2 calmodulin 2 (phosphorylase kinase, delta)
CALM3 calmodulin 3 (phosphorylase kinase, delta)
CAMKMT calmodulin-lysine N-methyltransferase
CASQ2 calsequestrin 2 (cardiac muscle)
CAVIN1 caveolae associated protein 1
CNTN3 contactin 3 (plasmacytoma associated)
CTRL chymotrypsin-like
FKBP1B FK506 binding protein 1B, 12.6 kDa
FXN frataxin
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
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KRIT1 KRIT1, ankyrin repeat containing
PICALM phosphatidylinositol binding clathrin assembly protein
RYR1 ryanodine receptor 1 (skeletal)
RYR2 ryanodine receptor 2 (cardiac)
SCN10A sodium channel, voltage gated, type X alpha subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SNAP91 synaptosomal-associated protein, 91kDa
TECRL trans-2,3-enoyl-CoA reductase-like
THEM5 thioesterase superfamily member 5
TRDN triadin