Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

RGD ID: 1352992
Species: Homo sapiens
RGD Object: Gene
Symbol: KCNJ2
Name: potassium inwardly rectifying channel subfamily J member 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)
KCNJ2 IEP 7247428RGDmRNA:increased expression:heart atrium 
KCNJ2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Atrial fibrillationPMID:15922306 PMID:17581963 PMID:19041665 PMID:19111761 PMID:22581653 PMID:23631430 PMID:25223803 PMID:25410959 PMID:25637381 PMID:25741868 PMID:28492532 PMID:28711067 PMID:29247119 PMID:31521807 PMID:34426522 PMID:34516623 PMID:35456365
Go Back to source page   Continue to Ontology report