brugada syndrome Gene Set

Dataset DISEASES Curated Gene-Disease Association Evidence Scores
Category disease or phenotype associations
Type disease
Description A heart conduction disease that is characterized by abnormal electrocardiogram (ECG) findings and an increased risk of sudden cardiac death. (Human Disease Ontology, DOID_0050451)
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Genes

9 genes involed in the disease brugada syndrome from the DISEASES Curated Gene-Disease Assocation Evidence Scores dataset.

Symbol Name
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CACNB2 calcium channel, voltage-dependent, beta 2 subunit
GPD1L glycerol-3-phosphate dehydrogenase 1-like
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
KCNE3 potassium channel, voltage gated subfamily E regulatory beta subunit 3
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
SCN5A sodium channel, voltage gated, type V alpha subunit