CAMK2A

calcium/calmodulin dependent protein kinase II alpha
OMIM: 114078
PanelMode of inheritanceDetails
1 panel
Component of the following Super Panels:
  • - Hypotonic infant
  • - Paediatric disorders
  • - White matter disorders - childhood onset
R-numbers: R29
Signed-off version 4.4
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Mental retardation, autosomal dominant 53, OMIM:617798, ?Mental retardation, autosomal recessive 63, OMIM:618095