Gene
CSNK2A1
casein kinase 2 alpha 1
- HGNC 2457↗(opens in a new tab)
- Ensembl gene ENSG00000101266↗(opens in a new tab)
- NCBI Gene 1457↗(opens in a new tab)
Summary
- Cytogenetic location
- 20p13
- Coordinates
- Chromosome 20: 472,498–543,790 (GRCh38)
- Exons
- 14 exons across 71.3 kb
- Protein
- 391 amino acids
- Also known as
- Cka1, Cka2
- MANE Select transcript
- ENST00000217244.9NM_177559.3
- Locus type
- gene with protein product
- Very high
- Confident
- Low
- Very low
Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
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Intellectual Disability
One of 233 genes linked to it
- ClinGen rates the link definitive
- 1 GenCC submitter rates it definitive or strong
How CSNK2A1 is laid out
- Coding sequence
- Untranslated region
- Intron
- Direction of transcription
- Known disease-causing sites
- Stretches short reads find hard
Exons of the gene's MANE Select transcript (release v1.5), from NCBI and EMBL-EBI, on the GRCh38 reference genome.
Chromosome bands from UCSC's GRCh38 ideogram (2022-10-29).
Nearby genes from Ensembl release 116, on GRCh38.
Exons make up 13 kb of the gene's 71.3 kb; 1,176 of those bases code for the protein.
How a genome test reads CSNK2A1
49
positions in CSNK2A1 where ClinVar classes a change as pathogenic or likely pathogenic
5 of them (10%) fall in regions short reads find hard.
- Low mappability (5 sites)Regions where 100 bp or 250 bp reads cannot be placed uniquely.
A whole genome covers all 71.3 kb of CSNK2A1, introns included, not only the 13 kb of exons.
Genes linked to the same conditions
- ACSL4acyl-CoA synthetase long chain family member 4Shares 1 condition
- ADKadenosine kinaseShares 1 condition
- ADNPactivity dependent neuroprotector homeoboxShares 1 condition
- AFF2ALF transcription elongation factor 2Shares 1 condition
- AHDC1AT-hook DNA binding motif containing 1Shares 1 condition
- ALKBH8alkB homolog 8, tRNA methyltransferaseShares 1 condition
- ANK3ankyrin 3Shares 1 condition
- ANKRD11ankyrin repeat domain 11Shares 1 condition
- AP1S2adaptor related protein complex 1 subunit sigma 2Shares 1 condition
- AP2M1adaptor related protein complex 2 subunit mu 1Shares 1 condition
- ARHGEF9Cdc42 guanine nucleotide exchange factor 9Shares 1 condition
- ARID1AAT-rich interaction domain 1AShares 1 condition
Traits linked to CSNK2A1
The Human Phenotype Ontology lists these as features of the rare conditions CSNK2A1 can cause. Each trait's page lists the other genes linked to it.
External links
Gene records
Transcript
Protein
Where this comes from
- HGNC: the gene's symbol, name, other symbols and location.
- MANE Select v1.5, from NCBI and EMBL-EBI: the transcript, its exons and coding sequence.
- GenCC and ClinGen, released 2026-10-16: which conditions the gene is linked to, and how strongly.
- The ACMG secondary findings list, SF v3.2.
- ClinVar and the GIAB stratifications: known disease-causing sites, and the regions short reads find hard.
- The Human Phenotype Ontology, release 2026-09-01: the traits linked to the gene. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
Cite this page
Dante Labs. (n.d.). CSNK2A1 gene: casein kinase 2 alpha 1. Retrieved 17 October 2026, from https://dantelabs.com/genes/csnk2a1
Dante Labs. CSNK2A1 gene: casein kinase 2 alpha 1 [Internet]. [cited 17 October 2026]. Available from: https://dantelabs.com/genes/csnk2a1
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