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CSNK2A1

casein kinase 2 alpha 1

HCNC Approved Symbol
CSNK2A1 (HGNC:2457)
Genomic Coordinates
20:472,498 - 543,790 (20p13)
Synonyms
Cka1, Cka2
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

19Patients

In total, 19 patients were diagnosed with a variant in the CSNK2A1 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

Global developmental delay
 7 (36.8%)
Microcephaly
 6 (31.6%)
Developmental delay
 3 (15.8%)
Learning difficulties
 3 (15.8%)
Epilepsy
 
2 (10.5%)
CSNK2A1 - Gene browser | 3billion