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 05/28/2024 MGI 6.13 |
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