Genomics England
GMS Panels
Panels
Genes and Entities

CSNK2B

casein kinase 2 beta
OMIM: 115441
PanelMode of inheritanceDetails
3 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 3.79
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CSNK2B-related developmental disorder (monoallelic)
Green
in Early onset or syndromic epilepsy
Component of the following Super Panels:
  • - Paediatric disorders
  • - Unexplained death in infancy and sudden unexplained death in childhood
R-numbers: R59
Signed-off version 4.134
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Poirier-Bienvenu neurodevelopmental syndrome, OMIM:618732, Poirier-Bienvenu neurodevelopmental syndrome, MONDO:0032889
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 5.343
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Poirier-Bienvenu neurodevelopmental syndrome, OMIM:618732, Poirier-Bienvenu neurodevelopmental syndrome, MONDO:0032889