Short Qt Syndrome Gene Set

Dataset	DisGeNET Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	An autosomal dominant disease that is characterized by heart arrhythmia defined as a short QT interval on an EKG (less than 300 ms) that does not significantly change with heart rate, tall and peaked T waves, and a structurally normal heart. (Human Disease Ontology, DOID_0050793)
External Link	https://www.disgenet.org/browser/0/1/0/C1865018
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Genes

10 genes associated with the disease Short Qt Syndrome in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol	Name
CACNA1C	calcium channel, voltage-dependent, L type, alpha 1C subunit
CACNA2D1	calcium channel, voltage-dependent, alpha 2/delta subunit 1
KCNE1	potassium channel, voltage gated subfamily E regulatory beta subunit 1
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
MYPN	myopalladin
RYR2	ryanodine receptor 2 (cardiac)
SLC4A3	solute carrier family 4 (anion exchanger), member 3
SNTA1	syntrophin, alpha 1