Brugada Syndrome Gene Set

Dataset	CTD Gene-Disease Associations
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)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:D053840
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Genes

5 genes/proteins associated with the disease Brugada Syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
SCN1B	sodium channel, voltage gated, type I beta subunit	2.88009
SCN5A	sodium channel, voltage gated, type V alpha subunit	2.88009
SCN10A	sodium channel, voltage gated, type X alpha subunit	2.88009
HEY2	hes-related family bHLH transcription factor with YRPW motif 2	2.88009
KCNH2	potassium channel, voltage gated eag related subfamily H, member 2	1.22821