KLK14
Kallikrein-14
Also known as: KLK-L6, KLK14_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P0G3
- Gene
- KLK14
- Ensembl
- ENSG00000129437
- Chromosome
- 19
- Canonical length
- 267 aa
- Protein class
- Cancer-related genes, Enzymes, Plasma proteins, Predicted secreted proteins
- Secretome location
- Secreted in other tissues
OverviewNCBI Gene
This gene encodes a member of the kallikrein subfamily of serine proteases that have diverse physiological functions such as regulation of blood pressure and desquamation. The altered expression of this gene is implicated in the progression of different cancers including breast and prostate tumors. The encoded protein is a precursor that is proteolytically processed to generate the functional enzyme. This gene is one of the fifteen kallikrein subfamily members located in a cluster on chromosome 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2015]
Canonical amino-acid sequenceUniProt
267 residues, UniProt reviewed canonical sequence.
>Q9P0G3|KLK14
1 MSLRVLGSGT WPSAPKMFLL LTALQVLAIA MTQSQEDENK IIGGHTCTRS SQPWQAALLA
61 GPRRRFLCGG ALLSGQWVIT AAHCGRPILQ VALGKHNLRR WEATQQVLRV VRQVTHPNYN
121 SRTHDNDLML LQLQQPARIG RAVRPIEVTQ ACASPGTSCR VSGWGTISSP IARYPASLQC
181 VNINISPDEV CQKAYPRTIT PGMVCAGVPQ GGKDSCQGDS GGPLVCRGQL QGLVSWGMER
241 CALPGYPGVY TNLCKYRSWI EETMRDKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against KLK14 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.31
- Highest tissue expression
- 9.9 nTPM
Expression across tissuesHPA
Tissue
- skin: 9.9 nTPM
- vagina: 4 nTPM
- cervix: 2.3 nTPM
- cerebellum: 2.1 nTPM
- breast: 1.5 nTPM
- basal ganglia: 1.3 nTPM
Single-cell type
- tuft cells: 12 nCPM
- breast hormone-responsive cells: 5.5 nCPM
- respiratory secretory cells: 3.7 nCPM
- suprabasal keratinocytes: 3.5 nCPM
- transitional alveolar cells: 2.3 nCPM
- retinal horizontal cells: 2 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: 3.3 nTPM
- cerebellum: 2.6 nTPM
- white matter: 2.4 nTPM
- basal ganglia: 2.3 nTPM
- hippocampal formation: 2.3 nTPM
- pons: 2.3 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)
- 1.57
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.39
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- epidermis morphogenesis
- fertilization
- negative regulation of G protein-coupled receptor signaling pathway
- positive regulation of G protein-coupled receptor signaling pathway
- protein maturation
- proteolysis
- seminal clot liquefaction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads KLK14 as an antibody target. Whether an autoantibody or antibody against KLK14 could matter depends on whether native KLK14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
KLK14 is annotated as secreted, so native KLK14 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label KLK14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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