ventricular tachycardia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0004756
Similar Terms
Downloads & Tools

Genes

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

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
CTNNA3 catenin (cadherin-associated protein), alpha 3
DSG2 desmoglein 2
DSP desmoplakin
GNAI2 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
JPH2 junctophilin 2
JUP junction plakoglobin
MYL2 myosin, light chain 2, regulatory, cardiac, slow
MYOZ2 myozenin 2
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
RYR2 ryanodine receptor 2 (cardiac)
SLC25A20 solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
TMEM43 transmembrane protein 43
TPM1 tropomyosin 1 (alpha)