tachycardia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A rapid heartrate that exceeds the range of the normal resting heartrate for age. (Human Phenotype Ontology, HP_0001649)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001649
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Genes

63 genes associated with the 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
ANK2 ankyrin 2, neuronal
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CACNB2 calcium channel, voltage-dependent, beta 2 subunit
CLIC2 chloride intracellular channel 2
CNBP CCHC-type zinc finger, nucleic acid binding protein
CPOX coproporphyrinogen oxidase
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
CTNNA3 catenin (cadherin-associated protein), alpha 3
DMPK dystrophia myotonica-protein kinase
DSG2 desmoglein 2
DSP desmoplakin
DST dystonin
DTNA dystrobrevin, alpha
EMD emerin
FBP1 fructose-1,6-bisphosphatase 1
FMO3 flavin containing monooxygenase 3
GATAD1 GATA zinc finger domain containing 1
GJA5 gap junction protein, alpha 5, 40kDa
GNAI2 guanine nucleotide binding protein (G protein), alpha inhibiting activity polypeptide 2
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
HMBS hydroxymethylbilane synthase
IKBKAP inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase complex-associated protein
JPH2 junctophilin 2
JUP junction plakoglobin
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
KIF1B kinesin family member 1B
LMNA lamin A/C
MYL2 myosin, light chain 2, regulatory, cardiac, slow
MYOZ2 myozenin 2
NAA10 N(alpha)-acetyltransferase 10, NatA catalytic subunit
NEXN nexilin (F actin binding protein)
NKX2-5 NK2 homeobox 5
NPPA natriuretic peptide A
NUP155 nucleoporin 155kDa
PGM1 phosphoglucomutase 1
PLN phospholamban
PPOX protoporphyrinogen oxidase
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
PTRF polymerase I and transcript release factor
RET ret proto-oncogene
RYR1 ryanodine receptor 1 (skeletal)
RYR2 ryanodine receptor 2 (cardiac)
SCN3B sodium channel, voltage gated, type III beta subunit
SCN4B sodium channel, voltage gated, type IV beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SCN9A sodium channel, voltage gated, type IX alpha subunit
SDHB succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SLC25A20 solute carrier family 25 (carnitine/acylcarnitine translocase), member 20
SMAD3 SMAD family member 3
TLL1 tolloid-like 1
TMEM43 transmembrane protein 43
TNNI3 troponin I type 3 (cardiac)
TNNT2 troponin T type 2 (cardiac)
TPM1 tropomyosin 1 (alpha)
TSHR thyroid stimulating hormone receptor
VHL von Hippel-Lindau tumor suppressor, E3 ubiquitin protein ligase