CSNK2A1
Casein kinase II subunit alpha
Also known as: Cka1, Cka2, CSK21_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P68400
- Gene
- CSNK2A1
- Ensembl
- ENSG00000101266
- Chromosome
- 20
- Canonical length
- 391 aa
- Protein class
- Disease related genes, Enzymes, Human disease related genes, Potential drug targets, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
Casein kinase II is a serine/threonine protein kinase that phosphorylates acidic proteins such as casein. It is involved in various cellular processes, including cell cycle control, apoptosis, and circadian rhythm. The kinase exists as a tetramer and is composed of an alpha, an alpha-prime, and two beta subunits. The alpha subunits contain the catalytic activity while the beta subunits undergo autophosphorylation. The protein encoded by this gene represents the alpha subunit. Multiple transcript variants encoding different protein isoforms have been found for this gene. [provided by RefSeq, Apr 2018]
Canonical amino-acid sequenceUniProt
391 residues, UniProt reviewed canonical sequence.
>P68400|CSNK2A1
1 MSGPVPSRAR VYTDVNTHRP REYWDYESHV VEWGNQDDYQ LVRKLGRGKY SEVFEAINIT
61 NNEKVVVKIL KPVKKKKIKR EIKILENLRG GPNIITLADI VKDPVSRTPA LVFEHVNNTD
121 FKQLYQTLTD YDIRFYMYEI LKALDYCHSM GIMHRDVKPH NVMIDHEHRK LRLIDWGLAE
181 FYHPGQEYNV RVASRYFKGP ELLVDYQMYD YSLDMWSLGC MLASMIFRKE PFFHGHDNYD
241 QLVRIAKVLG TEDLYDYIDK YNIELDPRFN DILGRHSRKR WERFVHSENQ HLVSPEALDF
301 LDKLLRYDHQ SRLTAREAME HPYFYTVVKD QARMGSSSMP GGSTPVSSAN MMSGISSVPT
361 PSPLGPLAGS PVIAAANPLG MPVPAAAGAQ QLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CSNK2A1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 104 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 104 nTPM
- tongue: 81 nTPM
- testis: 61 nTPM
- parathyroid gland: 55 nTPM
- heart muscle: 51 nTPM
- thymus: 48 nTPM
Single-cell type
- late primary spermatocytes: 229 nCPM
- late spermatids: 211 nCPM
- esophageal apical cells: 194 nCPM
- erythrocyte progenitors: 185 nCPM
- proximal tubule cells: 184 nCPM
- distal convoluted tubule cells: 183 nCPM
Immune cell
- basophil: 41 nTPM
- non-classical monocyte: 34 nTPM
- intermediate monocyte: 32 nTPM
- myeloid DC: 32 nTPM
- eosinophil: 29 nTPM
- plasmacytoid DC: 26 nTPM
Brain region
- choroid plexus: 78 nTPM
- cerebral cortex: 77 nTPM
- cerebellum: 74 nTPM
- white matter: 70 nTPM
- hippocampal formation: 69 nTPM
- thalamus: 64 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CSNK2A1.
Disease | AllUniProt
Conditions CSNK2A1 is implicated in, by any mechanism.
- Okur-Chung neurodevelopmental syndrome (OCNDS) MIM:617062
Disease | GeneticClinVar
80 pathogenic / likely-pathogenic of 269 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Okur-Chung neurodevelopmental syndrome
- Inborn genetic diseases
- CSNK2A1-related disorder
- See cases
- Neurodevelopmental delay
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.3
- gnomAD pLI
- 0.99
- gnomAD missense Z
- 3.71
- DepMap mean gene effect
- -0.13
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 13% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- apoptotic process
- DNA damage response
- double-strand break repair
- negative regulation of apoptotic signaling pathway
- negative regulation of double-strand break repair via homologous recombination
- negative regulation of proteasomal ubiquitin-dependent protein catabolic process
- negative regulation of signal transduction by p53 class mediator
- negative regulation of translation
- positive regulation of aggrephagy
- positive regulation of cell growth
- positive regulation of cell population proliferation
- positive regulation of protein catabolic process
- positive regulation of Wnt signaling pathway
- protein folding
- protein stabilization
- regulation of cell cycle
- regulation of chromosome separation
- rhythmic process
- signal transduction
- symbiont-mediated disruption of host cell PML body
- Wnt signaling pathway
Molecular functions
- ATP binding
- Hsp90 protein binding
- identical protein binding
- kinase activity
- protein serine kinase activity
- protein serine/threonine kinase activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CSNK2A1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CSNK2A1 as an antibody target. Whether an autoantibody or antibody against CSNK2A1 could matter depends on whether native CSNK2A1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CSNK2A1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label CSNK2A1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...