Genomics England
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Genes and Entities
CDC42BPB
CDC42 binding protein kinase beta
OMIM:
614062
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Panel
Mode of inheritance
Details
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Fetal anomalies
R-numbers:
R21
,
R412
Signed-off version 7.0
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Chilton-Okur-Chung neurodevelopmental syndrome, OMIM:619841