Atrioventricular Block Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A heart conduction disease that is characterized by the impairment of the conduction between the atria and ventricles of the heart. (Human Disease Ontology, DOID_0050820)
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Genes

11 genes associated with the Atrioventricular Block phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ADRA2B adrenoceptor alpha 2B
ARHGAP24 Rho GTPase activating protein 24
CAV1 caveolin 1, caveolae protein, 22kDa
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
KCNN3 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
SCN10A sodium channel, voltage gated, type X alpha subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
TBX5 T-box 5