KRT8
Keratin, type II cytoskeletal 8
Also known as: CARD2, CK-8, CK8, CYK8, K2C8, K2C8_HUMAN, K8, KO
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P05787
- Gene
- KRT8
- Ensembl
- ENSG00000170421
- Chromosome
- 12
- Canonical length
- 483 aa
- Protein class
- Cancer-related genes, Disease related genes, Human disease related genes, Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Intermediate filaments
OverviewNCBI Gene
This gene is a member of the type II keratin family clustered on the long arm of chromosome 12. Type I and type II keratins heteropolymerize to form intermediate-sized filaments in the cytoplasm of epithelial cells. The product of this gene typically dimerizes with keratin 18 to form an intermediate filament in simple single-layered epithelial cells. This protein plays a role in maintaining cellular structural integrity and also functions in signal transduction and cellular differentiation. Mutations in this gene cause cryptogenic cirrhosis. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012]
Canonical amino-acid sequenceUniProt
483 residues, UniProt reviewed canonical sequence.
>P05787|KRT8
1 MSIRVTQKSY KVSTSGPRAF SSRSYTSGPG SRISSSSFSR VGSSNFRGGL GGGYGGASGM
61 GGITAVTVNQ SLLSPLVLEV DPNIQAVRTQ EKEQIKTLNN KFASFIDKVR FLEQQNKMLE
121 TKWSLLQQQK TARSNMDNMF ESYINNLRRQ LETLGQEKLK LEAELGNMQG LVEDFKNKYE
181 DEINKRTEME NEFVLIKKDV DEAYMNKVEL ESRLEGLTDE INFLRQLYEE EIRELQSQIS
241 DTSVVLSMDN SRSLDMDSII AEVKAQYEDI ANRSRAEAES MYQIKYEELQ SLAGKHGDDL
301 RRTKTEISEM NRNISRLQAE IEGLKGQRAS LEAAIADAEQ RGELAIKDAN AKLSELEAAL
361 QRAKQDMARQ LREYQELMNV KLALDIEIAT YRKLLEGEES RLESGMQNMS IHTKTTSGYA
421 GGLSSAYGGL TSPGLSYSLG SSFGSGAGSS SFSRTSSSRA VVVKKIETRD GKLVSESSDV
481 LPKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KRT8 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)
- 0.54
- Highest tissue expression
- 1,282 nTPM
Expression across tissuesHPA
Tissue
- small intestine: 1,282 nTPM
- duodenum: 1,067 nTPM
- colon: 1,041 nTPM
- stomach: 768 nTPM
- pancreas: 578 nTPM
- rectum: 554 nTPM
Single-cell type
- colonocytes: 8,807 nCPM
- extravillous trophoblasts: 6,860 nCPM
- syncytiotrophoblasts: 6,236 nCPM
- enterocytes: 5,865 nCPM
- migrating cytotrophoblasts: 5,080 nCPM
- goblet cells: 3,744 nCPM
Immune cell
- plasmacytoid DC: 1.8 nTPM
- basophil: 1.1 nTPM
- myeloid DC: 0.8 nTPM
- NK-cell: 0.5 nTPM
- neutrophil: 0.4 nTPM
- intermediate monocyte: 0.3 nTPM
Brain region
- choroid plexus: 53 nTPM
- pons: 24 nTPM
- medulla oblongata: 16 nTPM
- hypothalamus: 15 nTPM
- midbrain: 15 nTPM
- basal ganglia: 9.6 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about KRT8.
Disease | AllUniProt
Conditions KRT8 is implicated in, by any mechanism.
- Cirrhosis (CIRRH) MIM:215600
Disease | ImmuneIEDB
Conditions an epitope on KRT8 was assayed in.
- viral infectious disease T cell
- coronary artery disease T cell
- rheumatoid arthritis T cell
ReferencesPubMed · IEDB
Publications for KRT8 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
4 publications
- Profile identification of disease-associated humoral antigens using AMIDA, a novel proteomics-based technology.
2004 · Cell Mol Life Sci · RCR 1.2 · 57 citations - Anti-cytokeratin antibodies in sera of the patients with autoimmune hepatitis.
2001 · Clin Exp Immunol · RCR 0.6 · 23 citations - Evaluation of CK8-specific autoantibodies in carcinomas of distinct localisations.
2006 · Anticancer Res · RCR 0.2 · 6 citations - Autoantibodies in small fiber neuropathy: frequency and clinical features associated with antibodies to the novel targets MX1 and DBNL.
2026 · J Neurol
Reference: T cellIEDB
3 publications
- T cell receptor fingerprinting enables in-depth characterization of the interactions governing recognition of peptide-MHC complexes.
2018 · Nat Biotechnol · RCR 2 · 73 citations - Immune responses to citrullinated and homocitrullinated peptides in healthy donors are not restricted to the HLA SE shared allele and can be selected into the memory pool.
2023 · Immunology · RCR 0.8 · 6 citations - Keratin 8 is a potential self-antigen in the coronary artery disease immunopeptidome: A translational approach.
2019 · PLoS One · RCR 0.5 · 12 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. IEDB — curated epitope assays from the Immune Epitope Database (Vita et al., Nucleic Acids Research 2019). Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 1.07
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.78
- DepMap mean gene effect
- -0.63
- DepMap dependency class
- common
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell differentiation involved in embryonic placenta development
- extrinsic apoptotic signaling pathway
- hepatocyte apoptotic process
- response to other organism
- tumor necrosis factor-mediated signaling pathway
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of KRT8 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 KRT8 as an antibody target. Whether an autoantibody or antibody against KRT8 could matter depends on whether native KRT8 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KRT8 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 KRT8 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...