Symbol Name ID |
Kcnn4
potassium intermediate/small conductance calcium-activated channel, subfamily N, member 4 MGI:1277957 |
Darker colors indicate more annotations |
Human Phenotypes | Splenomegaly |
Disease(s) Associated with KCNN4 | |
dehydrated hereditary stomatocytosis 2 |
Mouse Phenotypes | abnormal thymus morphology |
enlarged thymus |
small thymus |
enlarged spleen |
increased spleen weight |
abnormal spleen morphology |
increased spleen iron level |
abnormal T cell physiology |
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Availability | Mouse Genotype | ||||||||
Kcnn4em1(IMPC)Ccpcz/Kcnn4em1(IMPC)Ccpcz | |||||||||
Kcnn4tm1Jemn/Kcnn4tm1Jemn | |||||||||
Kcnn4tm1Rklr/Kcnn4tm1Rklr |
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 04/23/2024 MGI 6.23 |
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