shortened qt interval Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	Decreased time between the start of the Q wave and the end of the T wave as measured by the electrocardiogram (EKG). (Human Phenotype Ontology, HP_0012232)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0012232
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Genes

5 genes associated with the shortened qt interval phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
CACNA1C	calcium channel, voltage-dependent, L type, alpha 1C subunit
CACNB2	calcium channel, voltage-dependent, beta 2 subunit
KCNH2	potassium channel, voltage gated eag related subfamily H, member 2
KCNJ2	potassium channel, inwardly rectifying subfamily J, member 2
KCNQ1	potassium channel, voltage gated KQT-like subfamily Q, member 1