Genomics England
GMS Panels
Panels
Genes and Entities

CSNK2A1

casein kinase 2 alpha 1
OMIM: 115440
PanelMode of inheritanceDetails
5 panels
Green
in DDG2P
Component of the following Super Panels:
  • - Paediatric disorders
Signed-off version 4.15
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CSNK2A1 syndrome
Green
in Fetal anomalies
R-numbers: R21, R412
Signed-off version 4.195
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
CSNK2A1 syndrome, Okur-Chung neurodevelopmental syndrome, 617062
Green
in Intellectual disability
Component of the following Super Panels:
  • - Childhood onset leukodystrophy
  • - Hypotonic infant
  • - Paediatric disorders
R-numbers: R29
Signed-off version 7.51
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Okur-Chung neurodevelopmental syndrome, OMIM:617062
Green
in Malformations of cortical development
Component of the following Super Panels:
  • - Cerebral malformation
Signed-off version 6.3
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes
Okur-Chung neurodevelopmental syndrome, OMIM:617062
Green
in Severe microcephaly
R-numbers: R88
Signed-off version 6.8
MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Phenotypes
Okur-Chung neurodevelopmental syndrome, OMIM:617062