Congenital Long Qt Syndrome Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C1141890
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Genes

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

Symbol Name
AKAP9 A kinase (PRKA) anchor protein 9
ATN1 atrophin 1
ATP2B4 ATPase, Ca++ transporting, plasma membrane 4
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CALM1 calmodulin 1 (phosphorylase kinase, delta)
CALM2 calmodulin 2 (phosphorylase kinase, delta)
CAV3 caveolin 3
EDA ectodysplasin A
ERBB2 erb-b2 receptor tyrosine kinase 2
GJB6 gap junction protein, beta 6, 30kDa
GOLGA2 golgin A2
HAND2 heart and neural crest derivatives expressed 2
HARS1 histidyl-tRNA synthetase 1
HGS hepatocyte growth factor-regulated tyrosine kinase substrate
KCNA4 potassium channel, voltage gated shaker related subfamily A, member 4
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5
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
KCNK3 potassium channel, two pore domain subfamily K, member 3
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
SCD stearoyl-CoA desaturase (delta-9-desaturase)
SCN4B sodium channel, voltage gated, type IV beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SGK1 serum/glucocorticoid regulated kinase 1
SNTA1 syntrophin, alpha 1
SRSF5 serine/arginine-rich splicing factor 5