KRT39
Keratin, type I cytoskeletal 39
Also known as: K1C39_HUMAN, KA35
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6A163
- Gene
- KRT39
- Ensembl
- ENSG00000196859
- Chromosome
- 17
- Canonical length
- 491 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Mid piece,Principal piece,Annulus
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
491 residues, UniProt reviewed canonical sequence.
>Q6A163|KRT39
1 MDTKGCTTTN SPSTPCQNCS RITNVSTISS NNGCHPGGLT VNNCQPAGHV LRIPWDQGCQ
61 PTPRFCRKPI YLMNNFNARF SLDDCSWYGE GINSNEKETM QILNERLANY LQKVRMLERE
121 NAELESKIQE ESNKELPVLC PDYLSYYTTI EELQQKILCT KAENSRLVSQ IDNTKLTADD
181 LRAKYEAEVS LRQLVESDAN GLKQILNVLT LGKADLEAQV QSLKEELLCL KNNHKEEINS
241 LQCQLGERLD IEVTAAPSAD LNQVLQEMRC QYEPIMETNR KDVEQWFNTQ IEELNQQVVT
301 SSQQQQCCQK EIIELRRSVN TLEVELQAQH RMRDSQECIL TETEARYTAL LTQIQSLIDN
361 LEAQLAEIRC ALERQNQEYE ILLDVKSRLE CEITTYRSLL ESSDGKRPCY PRATKCEPSP
421 WTSCKSGAIE STAPACTSSS PCSLKEHCSA CGPLSRILVK ICTITKEIKD GKVISSYEHV
481 QPCFIIRPAK VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KRT39 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
- 4.8 nTPM
Expression across tissuesHPA
Tissue
- skin: 4.8 nTPM
- retina: 0.9 nTPM
- pituitary gland: 0.1 nTPM
- salivary gland: 0.1 nTPM
- adipose tissue: 0 nTPM
- adrenal gland: 0 nTPM
Single-cell type
- brain inhibitory neurons: 0.1 nCPM
- renal connecting tubule cells: 0.1 nCPM
- adipocytes: 0 nCPM
- adrenal cortex cells: 0 nCPM
- adrenal medulla cells: 0 nCPM
- alveolar cells type 1: 0 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
- cerebral cortex: 0.2 nTPM
- hypothalamus: 0.1 nTPM
- medulla oblongata: 0.1 nTPM
- pons: 0.1 nTPM
- thalamus: 0.1 nTPM
- white matter: 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)
- 1.22
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.16
- DepMap mean gene effect
- -0.01
- 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 KRT39 as an antibody target. Whether an autoantibody or antibody against KRT39 could matter depends on whether native KRT39 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KRT39 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 KRT39 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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