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Symbol Name ID |
Kcnh2
potassium voltage-gated channel, subfamily H (eag-related), member 2 MGI:1341722 |
| Darker colors indicate more annotations |
| Human Phenotypes | Prolonged QT interval |
Prolonged QTc interval |
Shortened QT interval |
Notched T wave |
Bradycardia |
Cardiac arrest |
Sudden cardiac death |
Palpitations |
Atrial fibrillation |
Paroxysmal atrial fibrillation |
Tachycardia |
Torsade de pointes |
Ventricular fibrillation |
Syncope |
| Disease(s) Associated with KCNH2 | ||||||||||||||
| long QT syndrome 2 | ||||||||||||||
| short QT syndrome |
| Mouse Phenotypes | decreased heart rate |
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| Availability | Mouse Genotype | |
| Kcnh2tm1Hjd/Kcnh2tm1Hjd | ||
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 05/14/2024 MGI 6.23 |
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