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


Contributing Projects:
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
The Jackson Laboratory