PanelApp (test)
  1. Genes and Genomic Entities
  2. CDC42BPB

CDC42BPB

CDC42 binding protein kinase beta
OMIM: 614062, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Green CDC42BPB in Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Chilton-Okur-Chung neurodevelopmental syndrome, MIM# 619841

Amber CDC42BPB in Genetic Epilepsy


Level 2: Neurology and neurodevelopmental disorders
Version 1.33

Component of the following Super Panels:

  • Progressive Neurological Conditions

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Amber
    • Literature
    Phenotypes
    • Chilton-Okur-Chung neurodevelopmental syndrome, MIM# 619841

    Green CDC42BPB in Intellectual disability syndromic and non-syndromic


    Level 2: Neurology and neurodevelopmental disorders
    Version 0.6063

    		review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • Literature
    Phenotypes
    • Chilton-Okur-Chung neurodevelopmental syndrome, MIM# 619841