Genes in panel

Early onset or syndromic epilepsy

Gene: CSNK1A1

No list

CSNK1A1 (casein kinase 1 alpha 1)
EnsemblGeneIds (GRCh38): ENSG00000113712
EnsemblGeneIds (GRCh37): ENSG00000113712
OMIM: 600505, Gene2Phenotype
CSNK1A1 is in 1 panel

1 review

Alexandra Njegic (Leeds Teaching Hospital Trust)

I don't know

PMID: 40156289 describes 2 unrelated families with de novo variants in CSNK1A1 (proband 1 harboured a small del variant, proband 2 harboured a missense variant, both were shown to have early-onset epileptic encephalopathy); confirmed variant on Sanger (obtained from WES). Mechanism of disease proposed to be due to reduced interactions between CSNK1A1 and β-catenin in variant CSNK1A1, resulting in excessive intracellular β-catenin and aberrant expression of several downstream genes. Only 2 families reported in the literature.
Sources: Literature
Created: 6 Oct 2026, 1:46 p.m.

Mode of inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown

Phenotypes
Infantile spasms syndrome

Publications

Details

Mode of Inheritance
MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Sources
Phenotypes
  • Infantile spasms syndrome
OMIM
600505
Clinvar variants
Variants in CSNK1A1
Penetrance
unknown
Publications
Panels with this gene

History Filter Activity

6 Oct 2026, Gel status: 0

Created, Added New Source, Set mode of inheritance, Set publications, Set Phenotypes, Set penetrance

Alexandra Njegic (Leeds Teaching Hospital Trust)

gene: CSNK1A1 was added gene: CSNK1A1 was added to Early onset or syndromic epilepsy. Sources: Literature Mode of inheritance for gene: CSNK1A1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: CSNK1A1 were set to 40156289 Phenotypes for gene: CSNK1A1 were set to Infantile spasms syndrome Penetrance for gene: CSNK1A1 were set to unknown Review for gene: CSNK1A1 was set to AMBER