heart conduction disease Gene Set

Dataset DISEASES Curated Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description A cardiovascular system disease that involves the heart's electrical conduction system. (Human Disease Ontology, DOID_10273)
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Genes

21 genes involed in the disease heart conduction disease from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CACNB2 calcium channel, voltage-dependent, beta 2 subunit
GATA5 GATA binding protein 5
GJA5 gap junction protein, alpha 5, 40kDa
GPD1L glycerol-3-phosphate dehydrogenase 1-like
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MYH6 myosin, heavy chain 6, cardiac muscle, alpha
NPPA natriuretic peptide A
NUP155 nucleoporin 155kDa
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
SCN1B sodium channel, voltage gated, type I beta subunit
SCN2B sodium channel, voltage gated, type II beta subunit
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