Symbol Name ID |
Camk2b
calcium/calmodulin-dependent protein kinase II, beta MGI:88257 |
Darker colors indicate more annotations |
Human Phenotypes | Microcephaly |
Disease(s) Associated with CAMK2B | |
autosomal dominant intellectual developmental disorder 54 |
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 04/09/2024 MGI 6.23 |
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