Symbol Name ID |
Kcnj2
potassium inwardly-rectifying channel, subfamily J, member 2 MGI:104744 |
Darker colors indicate more annotations |
Human Phenotypes | Dilated cardiomyopathy |
Prolonged QT interval |
Prolonged QTc interval |
Abnormal T-wave |
Prominent U wave |
Palpitations |
Atrial fibrillation |
Polymorphic ventricular tachycardia |
Ventricular arrhythmia |
Premature ventricular contraction |
Bidirectional ventricular ectopy |
Polymorphic and polytopic ventricular extrasystoles |
Torsade de pointes |
Myocardial infarction |
Syncope |
Disease(s) Associated with KCNJ2 | |||||||||||||||
Andersen-Tawil syndrome | |||||||||||||||
familial atrial fibrillation |
Mouse Phenotypes | abnormal vasodilation |
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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 07/02/2024 MGI 6.13 |
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