CXCL17
C-X-C motif chemokine 17
Also known as: CXL17_HUMAN, Dcip1, DMC, UNQ473, VCC1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6UXB2
- Gene
- CXCL17
- Ensembl
- ENSG00000189377
- Chromosome
- 19
- Canonical length
- 119 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
The protein encoded by this gene is a mucosal chemokine that attracts immature dendritic cells and blood monocytes to the lungs. The encoded protein also promotes tumorigenesis through an angiogenic activity. Finally, this protein exhibits strong antimicrobial activity against E. coli, S. aureus, Salmonella, P. aeruginosa, and C. albicans. Two transcript variants, one protein-coding and the other non-protein coding, have been found for this gene. [provided by RefSeq, Dec 2015]
Canonical amino-acid sequenceUniProt
119 residues, UniProt reviewed canonical sequence.
>Q6UXB2|CXCL17
1 MKVLISSLLL LLPLMLMSMV SSSLNPGVAR GHRDRGQASR RWLQEGGQEC ECKDWFLRAP
61 RRKFMTVSGL PKKQCPCDHF KGNVKKTRHQ RHHRKPNKHS RACQQFLKQC QLRSFALPLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CXCL17 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)
- 0.59
- Highest tissue expression
- 338 nTPM
Expression across tissuesHPA
Tissue
- stomach: 338 nTPM
- salivary gland: 146 nTPM
- lung: 140 nTPM
- esophagus: 126 nTPM
- urinary bladder: 44 nTPM
- pancreas: 43 nTPM
Single-cell type
- esophageal apical cells: 2,922 nCPM
- gastric chief cells: 1,910 nCPM
- respiratory secretory cells: 1,436 nCPM
- conjunctival goblet cells: 1,283 nCPM
- parietal cells: 1,114 nCPM
- submucosal glandular cells: 945 nCPM
Immune cell
- eosinophil: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebellum: 1.8 nTPM
- amygdala: 1.7 nTPM
- cerebral cortex: 1.6 nTPM
- basal ganglia: 1.4 nTPM
- white matter: 1.4 nTPM
- hippocampal formation: 1.2 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)
- 1.52
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.4
- DepMap mean gene effect
- -0.07
- DepMap dependency class
- none
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
- angiogenesis
- cell differentiation
- chemokine-mediated signaling pathway
- leukocyte chemotaxis
- lymphocyte chemotaxis
- macrophage chemotaxis
- monocyte chemotaxis
- negative regulation of inflammatory response
- neutrophil chemotaxis
- positive regulation of cytosolic calcium ion concentration
- positive regulation of ERK1 and ERK2 cascade
- positive regulation of macrophage chemotaxis
- positive regulation of monocyte chemotaxis
- positive regulation of vascular endothelial growth factor production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- C-X-C motif chemokine 17
- VEGF co-regulated chemokine 1
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CXCL17 as an antibody target. Whether an autoantibody or antibody against CXCL17 could matter depends on whether native CXCL17 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CXCL17 is annotated as secreted, so native CXCL17 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 CXCL17 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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