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