qt interval Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description The QT interval is a measure of the time between the start of the Q wave and the end of the T wave in the heart's electrical cycle (Experimental Factor Ontology, EFO_0004682)
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Genes

33 genes associated with the disease qt interval in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACOT7 acyl-CoA thioesterase 7
ARHGAP10 Rho GTPase activating protein 10
ASF1A anti-silencing function 1A histone chaperone
ATP1B1 ATPase, Na+/K+ transporting, beta 1 polypeptide
CEP85L centrosomal protein 85kDa-like
CLEC16A C-type lectin domain family 16, member A
CNOT1 CCR4-NOT transcription complex, subunit 1
ELMO1 engulfment and cell motility 1
GINS3 GINS complex subunit 3 (Psf3 homolog)
GOT2 glutamic-oxaloacetic transaminase 2, mitochondrial
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
LIG3 ligase III, DNA, ATP-dependent
LITAF lipopolysaccharide-induced TNF factor
NDRG4 NDRG family member 4
NOS1AP nitric oxide synthase 1 (neuronal) adaptor protein
NPHP4 nephronophthisis 4
OLFML2B olfactomedin-like 2B
PDE3A phosphodiesterase 3A, cGMP-inhibited
PLEKHG5 pleckstrin homology domain containing, family G (with RhoGef domain) member 5
PLN phospholamban
PTPRG protein tyrosine phosphatase, receptor type, G
RFFL ring finger and FYVE-like domain containing E3 ubiquitin protein ligase
RNF207 ring finger protein 207
SCN5A sodium channel, voltage gated, type V alpha subunit
SLC35F1 solute carrier family 35, member F1
SLC38A7 solute carrier family 38, member 7
SNN stannin
TCL6 T-cell leukemia/lymphoma 6 (non-protein coding)
TNFRSF17 tumor necrosis factor receptor superfamily, member 17
TTN titin
ZC3H7A zinc finger CCCH-type containing 7A