atrial fibrillation Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A heart conduction disease that is characterized by uncoordinated electrical activity in the heart's upper chambers (the atria), which causes the heartbeat to become fast and irregular and has symptoms palpitations, weakness, fatigue, lightheadedness, dizziness, confusion, shortness of breath and chest pain. (Human Disease Ontology, DOID_0060224)
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36 genes associated with the disease atrial fibrillation in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ACE angiotensin I converting enzyme
ADRB1 adrenoceptor beta 1
AGT angiotensinogen (serpin peptidase inhibitor, clade A, member 8)
AGTR1 angiotensin II receptor, type 1
CD200 CD200 molecule
CETP cholesteryl ester transfer protein, plasma
CNTN5 contactin 5
CRP C-reactive protein, pentraxin-related
CYP11B2 cytochrome P450, family 11, subfamily B, polypeptide 2
CYP2C9 cytochrome P450, family 2, subfamily C, polypeptide 9
CYP2D6 cytochrome P450, family 2, subfamily D, polypeptide 6
ESR1 estrogen receptor 1
F13A1 coagulation factor XIII, A1 polypeptide
GJA5 gap junction protein, alpha 5, 40kDa
GNB3 guanine nucleotide binding protein (G protein), beta polypeptide 3
HMCN1 hemicentin 1
KCNA5 potassium channel, voltage gated shaker related subfamily A, member 5
KCNE1 potassium channel, voltage gated subfamily E regulatory beta subunit 1
KCNE5 potassium channel, voltage gated subfamily E regulatory beta subunit 5
KCNH2 potassium channel, voltage gated eag related subfamily H, member 2
KCNJ5 potassium channel, inwardly rectifying subfamily J, member 5
KCNN3 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 3
LRRC63 leucine rich repeat containing 63
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NOS3 nitric oxide synthase 3 (endothelial cell)
NPPA natriuretic peptide A
PITX2 paired-like homeodomain 2
RAD51B RAD51 paralog B
RBFOX1 RNA binding protein, fox-1 homolog (C. elegans) 1
SCN3B sodium channel, voltage gated, type III beta subunit
SPSB4 splA/ryanodine receptor domain and SOCS box containing 4
TCF12 transcription factor 12
USO1 USO1 vesicle transport factor
VKORC1 vitamin K epoxide reductase complex, subunit 1
WDPCP WD repeat containing planar cell polarity effector
ZFHX3 zinc finger homeobox 3