primary atrial arrhythmia Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description A type of supraventricular tachycardia in which the atria are the principal site of electrophysiologic disturbance. (Human Phenotype Ontology, HP_0001692)
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35 genes associated with the primary atrial arrhythmia phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ABCC9 ATP-binding cassette, sub-family C (CFTR/MRP), member 9
ANK2 ankyrin 2, neuronal
CACNA1C calcium channel, voltage-dependent, L type, alpha 1C subunit
CACNB2 calcium channel, voltage-dependent, beta 2 subunit
CLIC2 chloride intracellular channel 2
CSRP3 cysteine and glycine-rich protein 3 (cardiac LIM protein)
DMPK dystrophia myotonica-protein kinase
DTNA dystrobrevin, alpha
EMD emerin
GATAD1 GATA zinc finger domain containing 1
GJA5 gap junction protein, alpha 5, 40kDa
HCN4 hyperpolarization activated cyclic nucleotide gated potassium channel 4
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5
KCNE2 potassium channel, voltage gated subfamily E regulatory beta subunit 2
KCNJ2 potassium channel, inwardly rectifying subfamily J, member 2
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
KCNQ1 potassium channel, voltage gated KQT-like subfamily Q, member 1
LMNA lamin A/C
MYOZ2 myozenin 2
NEXN nexilin (F actin binding protein)
NKX2-5 NK2 homeobox 5
NPPA natriuretic peptide A
NUP155 nucleoporin 155kDa
PLN phospholamban
PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit
PTRF polymerase I and transcript release factor
RYR2 ryanodine receptor 2 (cardiac)
SCN3B sodium channel, voltage gated, type III beta subunit
SCN4B sodium channel, voltage gated, type IV beta subunit
SCN5A sodium channel, voltage gated, type V alpha subunit
SMAD3 SMAD family member 3
TLL1 tolloid-like 1
TMEM43 transmembrane protein 43
TNNI3 troponin I type 3 (cardiac)
TNNT2 troponin T type 2 (cardiac)