torsade de pointes Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	A type of ventricular tachycardia characterized by polymorphioc QRS complexes that change in amplitue and cycle length, and thus have the appearance of oscillating around the baseline in the EKG. (Human Phenotype Ontology, HP_0001664)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0001664
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Genes

7 genes associated with the torsade de pointes phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
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
KCNQ1	potassium channel, voltage gated KQT-like subfamily Q, member 1
NAA10	N(alpha)-acetyltransferase 10, NatA catalytic subunit
SCN5A	sodium channel, voltage gated, type V alpha subunit
SNTA1	syntrophin, alpha 1