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GENE - TERM ANNOTATION REPORT

RGD ID: 731917
Species: Homo sapiens
RGD Object: Gene
Symbol: KCNE2
Name: potassium voltage-gated channel subfamily E regulatory subunit 2
Acc ID: DOID:0060224
Term: atrial fibrillation
Definition: 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. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Atrial_fibrillation "DO" "DO", http://www.mayoclinic.org/diseases-conditions/atrial-fibrillation/basics/definition/con-20027014 "DO" "DO", http://www.nhlbi.nih.gov/health/health-topics/topics/af "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
KCNE2 IAGP 1580501RGD  
KCNE2 EXP 11554173CTDCTD Direct Evidence: marker/mechanismPMID:15368194
KCNE2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Atrial fibrillationPMID:15368194 PMID:16487223 PMID:22581653 PMID:24681347 PMID:25741868 PMID:28492532
KCNE2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Atrial fibrillationPMID:18006559 PMID:22581653
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