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Symbol Name ID |
Kcnj2
potassium inwardly-rectifying channel, subfamily J, member 2 MGI:104744 |
| Darker colors indicate more annotations |
| Human Phenotypes | Left atrial enlargement |
Left ventricular hypertrophy |
Right ventricular dilatation |
Dilated cardiomyopathy |
Stroke |
Reduced left ventricular ejection fraction |
Elevated left ventricular end-diastolic diameter |
Aortic valve stenosis |
Tricuspid regurgitation |
Hypertension |
Prolonged P wave |
Prolonged PR interval |
Prolonged QRS complex |
Prolonged QT interval |
Prolonged QTc interval |
Shortened QT interval |
ST segment elevation |
Abnormal T-wave |
Prominent U wave |
Sinus bradycardia |
Bradycardia |
Cardiac arrest |
Sudden cardiac death |
Palpitations |
Atrial fibrillation |
Paroxysmal atrial fibrillation |
Permanent atrial fibrillation |
Atrial flutter |
Premature atrial contractions |
Supraventricular tachycardia |
Tachycardia |
Polymorphic ventricular tachycardia |
Ventricular arrhythmia |
Premature ventricular contraction |
Bidirectional ventricular ectopy |
Polymorphic and polytopic ventricular extrasystoles |
Torsade de pointes |
Ventricular fibrillation |
Myocardial infarction |
Syncope |
| Disease(s) Associated with KCNJ2 | ||||||||||||||||||||||||||||||||||||||||
| Andersen-Tawil syndrome | ||||||||||||||||||||||||||||||||||||||||
| familial atrial fibrillation | ||||||||||||||||||||||||||||||||||||||||
| short QT syndrome |
| Mouse Phenotypes | abnormal vasodilation |
|
| Availability | Mouse Genotype | |
| Kcnj2tm1Swz/Kcnj2tm1Swz | ||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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