atrioventricular block Gene Set

Dataset HPO Gene-Disease 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)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001678
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Genes

12 genes associated with the atrioventricular block phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
AGXT alanine-glyoxylate aminotransferase
DMPK dystrophia myotonica-protein kinase
EMD emerin
GJA1 gap junction protein, alpha 1, 43kDa
GJA5 gap junction protein, alpha 5, 40kDa
GPD1L glycerol-3-phosphate dehydrogenase 1-like
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
PTPN11 protein tyrosine phosphatase, non-receptor type 11
SCN4B sodium channel, voltage gated, type IV beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SLC25A20 solute carrier family 25 (carnitine/acylcarnitine translocase), member 20