KRT23
Keratin, type I cytoskeletal 23
Also known as: CK23, DKFZP434G032, HAIK1, K1C23_HUMAN, K23, MGC26158
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9C075
- Gene
- KRT23
- Ensembl
- ENSG00000108244
- Chromosome
- 17
- Canonical length
- 422 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Intermediate filaments,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a member of the keratin family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. The type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. The type I cytokeratin genes are clustered in a region of chromosome 17q12-q21. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Sep 2013]
Canonical amino-acid sequenceUniProt
422 residues, UniProt reviewed canonical sequence.
>Q9C075|KRT23
1 MNSGHSFSQT PSASFHGAGG GWGRPRSFPR APTVHGGAGG ARISLSFTTR SCPPPGGSWG
61 SGRSSPLLGG NGKATMQNLN DRLASYLEKV RALEEANMKL ESRILKWHQQ RDPGSKKDYS
121 QYEENITHLQ EQIVDGKMTN AQIILLIDNA RMAVDDFNLK YENEHSFKKD LEIEVEGLRR
181 TLDNLTIVTT DLEQEVEGMR KELILMKKHH EQEMEKHHVP SDFNVNVKVD TGPREDLIKV
241 LEDMRQEYEL IIKKKHRDLD TWYKEQSAAM SQEAASPATV QSRQGDIHEL KRTFQALEID
301 LQTQYSTKSA LENMLSETQS RYSCKLQDMQ EIISHYEEEL TQLRHELERQ NNEYQVLLGI
361 KTHLEKEITT YRRLLEGESE GTREESKSSM KVSATPKIKA ITQETINGRL VLCQVNEIQK
421 HALocalizationUniProt · AlphaFold · HPA
Whether an antibody against KRT23 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)
- 0.55
- Highest tissue expression
- 165 nTPM
Expression across tissuesHPA
Tissue
- skin: 165 nTPM
- salivary gland: 135 nTPM
- testis: 21 nTPM
- prostate: 20 nTPM
- placenta: 15 nTPM
- breast: 13 nTPM
Single-cell type
- syncytiotrophoblasts: 590 nCPM
- migrating cytotrophoblasts: 120 nCPM
- endometrial secretory cells: 105 nCPM
- breast secretory cells: 83 nCPM
- cytotrophoblasts: 72 nCPM
- late primary spermatocytes: 55 nCPM
Immune cell
- neutrophil: 0.9 nTPM
- eosinophil: 0.5 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- hippocampal formation: 0.2 nTPM
- amygdala: 0.1 nTPM
- basal ganglia: 0.1 nTPM
- cerebral cortex: 0.1 nTPM
- hypothalamus: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
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)
- 1.34
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.24
- DepMap mean gene effect
- -0.03
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KRT23 as an antibody target. Whether an autoantibody or antibody against KRT23 could matter depends on whether native KRT23 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KRT23 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 KRT23 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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