prolonged qt interval Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description increase in the length of time required for ventricular depolarization and repolarization to occur, usually as a result of increased repolarization time, and is measured from the beginning of the QRS complex to the end of the T wave (Mammalian Phenotype Ontology, MP_0003233)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001657
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Genes

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

Symbol Name
AKAP9 A kinase (PRKA) anchor protein 9
ANK2 ankyrin 2, neuronal
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CAV3 caveolin 3
DNAJC19 DnaJ (Hsp40) homolog, subfamily C, member 19
GMPPB GDP-mannose pyrophosphorylase B
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
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
MECP2 methyl CpG binding protein 2
PTRF polymerase I and transcript release factor
SCN4B sodium channel, voltage gated, type IV beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SNTA1 syntrophin, alpha 1
TRPM4 transient receptor potential cation channel, subfamily M, member 4