Arrhythmia Gene Set

Dataset HuGE Navigator Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Any cardiac rhythm other than the normal sinus rhythm. Such a rhythm may be either of sinus or ectopic origin and either regular or irregular. An arrhythmia may be due to a disturbance in impulse formation or conduction or both. (Human Phenotype Ontology, HP_0011675)
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Genes

16 genes associated with the Arrhythmia phenotype by text-mining GWAS publications from the HuGE Navigator Gene-Phenotype Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
CAV3 caveolin 3
CYP1A2 cytochrome P450, family 1, subfamily A, polypeptide 2
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
DMPK dystrophia myotonica-protein kinase
ECE1 endothelin converting enzyme 1
GNB3 guanine nucleotide binding protein (G protein), beta polypeptide 3
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
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LMNA lamin A/C
MT-TL1 tRNA
SCN5A sodium channel, voltage gated, type V alpha subunit
UGT1A4 UDP glucuronosyltransferase 1 family, polypeptide A4