|
Symbol Name ID |
Kcnj2
potassium inwardly-rectifying channel, subfamily J, member 2 MGI:104744 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hypokalemia |
Exercise intolerance |
| Disease(s) Associated with KCNJ2 | ||
| Andersen-Tawil syndrome | ||
| familial atrial fibrillation |
| Mouse Phenotypes | cyanosis |
dehydration |
|
| 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) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/16/2024 MGI 6.23 |
|
|
|
||
Analysis Tools