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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 | Scapular winging |
Muscle weakness |
Episodic flaccid weakness |
| Disease(s) Associated with KCNJ2 | |||
| Andersen-Tawil syndrome |
| 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 04/16/2024 MGI 6.23 |
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