PanelApp (test)
  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 Mendeliome


Version 1.1902

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Poirier-Bienvenu neurodevelopmental syndrome , MIM#618732
  • Craniodigital syndrome-intellectual disability syndrome MONDO:0015463

Green CSNK2B 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 Green
    • Victorian Clinical Genetics Services
    • Australian Genomics Health Alliance Epilepsy Flagship
    Phenotypes
    • Poirier-Bienvenu neurodevelopmental syndrome , MIM#618732

    Green CSNK2B 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
    • Genetic Health Queensland
    Phenotypes
    • Poirier-Bienvenu neurodevelopmental syndrome , MIM#618732