KRT27
Keratin, type I cytoskeletal 27
Also known as: K1C27_HUMAN, KRT25C
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z3Y8
- Gene
- KRT27
- Ensembl
- ENSG00000171446
- Chromosome
- 17
- Canonical length
- 459 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a member of the type I (acidic) keratin family, which belongs to the superfamily of intermediate filament (IF) proteins. Keratins are heteropolymeric structural proteins which form the intermediate filament. These filaments, along with actin microfilaments and microtubules, compose the cytoskeleton of epithelial cells. The type I keratin genes are clustered in a region of chromosome 17q12-q21. [provided by RefSeq, Jul 2009]
Canonical amino-acid sequenceUniProt
459 residues, UniProt reviewed canonical sequence.
>Q7Z3Y8|KRT27
1 MSVRFSSTSR RLGSCGGTGS VRLSSGGAGF GAGNTCGVPG IGSGFSCAFG GSSSAGGYGG
61 GLGGGSASCA AFTGNEHGLL SGNEKVTMQN LNDRLASYLE NVRALEEANA DLEQKIKGWY
121 EKFGPGSCRG LDHDYSRYFP IIDELKNQII SATTSNAHVV LQNDNARLTA DDFRLKFENE
181 LALHQSVEAD INGLRRVLDE LTLCRTDLEI QLETLSEELA YLKKNHEEEM KALQCAAGGN
241 VNVEMNAAPG VDLTVLLNNM RAEYEALAEQ NRRDAEAWFN EKSASLQQQI SDDAGATTSA
301 RNELIEMKRT LQTLEIELQS LLATKHSLEC SLTETESNYC AQLAQIQAQI GALEEQLHQV
361 RTETEGQKLE YEQLLDIKVH LEKEIETYCL LIDGEDGSCS KSKGYGGPGN QTKDSSKTTI
421 VKTVVEEIDP RGKVLSSRVH TVEEKSTKVN NKNEQRVSSLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KRT27 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
- 65 nTPM
Expression across tissuesHPA
Tissue
- skin: 65 nTPM
- adipose tissue: 1.4 nTPM
- salivary gland: 1 nTPM
- breast: 0.9 nTPM
- testis: 0.2 nTPM
- gallbladder: 0.1 nTPM
Single-cell type
- ocular epithelial cells: 12 nCPM
- melanocytes: 8.1 nCPM
- undifferentiated spermatogonia: 3.6 nCPM
- epididymal basal cells: 3.4 nCPM
- alveolar cells type 2: 3 nCPM
- medullary thymic epithelial cells: 2.4 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- hypothalamus: 0.2 nTPM
- amygdala: 0 nTPM
- basal ganglia: 0 nTPM
- cerebellum: 0 nTPM
- cerebral cortex: 0 nTPM
- choroid plexus: 0 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)
- 1.09
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.04
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- epithelial cell differentiation
- hair follicle morphogenesis
- intermediate filament organization
- morphogenesis of an epithelium
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KRT27 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 KRT27 as an antibody target. Whether an autoantibody or antibody against KRT27 could matter depends on whether native KRT27 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KRT27 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 KRT27 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...