CCL27
C-C motif chemokine 27
Also known as: ALP, CCL27_HUMAN, CTACK, CTAK, ESkine, ILC, PESKY, SCYA27, skinkine
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9Y4X3
- Gene
- CCL27
- Ensembl
- ENSG00000213927
- Chromosome
- 9
- Canonical length
- 112 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
This gene is one of several CC cytokine genes clustered on the p-arm of chromosome 9. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The protein encoded by this gene is chemotactic for skin-associated memory T lymphocytes. This cytokine may also play a role in mediating homing of lymphocytes to cutaneous sites. It specifically binds to chemokine receptor 10 (CCR10). Studies of a similar murine protein indicate that these protein-receptor interactions have a pivotal role in T cell-mediated skin inflammation. [provided by RefSeq, Sep 2014]
Canonical amino-acid sequenceUniProt
112 residues, UniProt reviewed canonical sequence.
>Q9Y4X3|CCL27
1 MKGPPTFCSL LLLSLLLSPD PTAAFLLPPS TACCTQLYRK PLSDKLLRKV IQVELQEADG
61 DCHLQAFVLH LAQRSICIHP QNPSLSQWFE HQERKLHGTL PKLNFGMLRK MGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCL27 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)
- 0.45
- Highest tissue expression
- 457 nTPM
Expression across tissuesHPA
Tissue
- skin: 457 nTPM
- breast: 26 nTPM
- thymus: 4.3 nTPM
- epididymis: 2.9 nTPM
- bone marrow: 1.5 nTPM
- skeletal muscle: 1.3 nTPM
Single-cell type
- basal keratinocytes: 4.8 nCPM
- suprabasal keratinocytes: 2.9 nCPM
- astrocytes: 0.9 nCPM
- bergmann glia: 0.8 nCPM
- brain excitatory neurons: 0.3 nCPM
- brain inhibitory neurons: 0.3 nCPM
Immune cell
- T-reg: 0.3 nTPM
- naive B-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebellum: 5.6 nTPM
- cerebral cortex: 2.8 nTPM
- white matter: 2.8 nTPM
- medulla oblongata: 2.4 nTPM
- pons: 2.3 nTPM
- midbrain: 2.2 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)
- 1.65
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.41
- DepMap mean gene effect
- -0.14
- 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
- antimicrobial humoral immune response mediated by antimicrobial peptide
- cell-cell signaling
- cellular response to lipopolysaccharide
- chemotaxis
- immune response
- inflammatory response
- neutrophil chemotaxis
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CCL27 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 CCL27 as an antibody target. Whether an autoantibody or antibody against CCL27 could matter depends on whether native CCL27 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCL27 is annotated as secreted, so native CCL27 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 CCL27 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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