1. Genes and Genomic Entities
  2. CSNK2B

CSNK2B

casein kinase 2 beta
OMIM: 115441, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels
Green CSNK2B in DDG2P


Version 6.438
Latest signed off version: v6.0 (30 Apr 2025)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • DD-Gene2Phenotype
    • Expert Review Green
    Phenotypes
    • CSNK2B-related developmental disorder (monoallelic)
    Green CSNK2B in Early onset or syndromic epilepsy


    Level 2: Neurology
    Version 8.159
    Latest signed off version: v8.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Paediatric disorders
  • Unexplained death in infancy and sudden unexplained death in childhood

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Wessex and West Midlands GLH
    • NHS GMS
    • Expert Review Green
    • Victorian Clinical Genetics Services
    Phenotypes
    • Poirier-Bienvenu neurodevelopmental syndrome, OMIM:618732
    • Poirier-Bienvenu neurodevelopmental syndrome, MONDO:0032889
    Green CSNK2B in Intellectual disability


    Level 2: Developmental disorders
    Version 9.330
    Latest signed off version: v9.0 (30 Apr 2025)

    Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Green
    • Victorian Clinical Genetics Services
    • Literature
    Phenotypes
    • Poirier-Bienvenu neurodevelopmental syndrome, OMIM:618732
    • Poirier-Bienvenu neurodevelopmental syndrome, MONDO:0032889