CCL13
C-C motif chemokine 13
Also known as: CCL13_HUMAN, CKb10, MCP-4, MGC17134, NCC-1, SCYA13, SCYL1
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q99616
- Gene
- CCL13
- Ensembl
- ENSG00000181374
- Chromosome
- 17
- Canonical length
- 98 aa
- Protein class
- Cancer-related genes, Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for monocytes, lymphocytes, basophils and eosinophils, but not neutrophils. This chemokine plays a role in accumulation of leukocytes during inflammation. It may also be involved in the recruitment of monocytes into the arterial wall during artherosclerosis. [provided by RefSeq, Sep 2014]
Canonical amino-acid sequenceUniProt
98 residues, UniProt reviewed canonical sequence.
>Q99616|CCL13
1 MKVSAVLLCL LLMTAAFNPQ GLAQPDALNV PSTCCFTFSS KKISLQRLKS YVITTSRCPQ
61 KAVIFRTKLG KEICADPKEK WVQNYMKHLG RKAHTLKTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCL13 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)
- 0.46
- Highest tissue expression
- 31 nTPM
Expression across tissuesHPA
Tissue
- colon: 31 nTPM
- urinary bladder: 28 nTPM
- small intestine: 26 nTPM
- rectum: 24 nTPM
- adipose tissue: 22 nTPM
- lung: 21 nTPM
Single-cell type
- hofbauer cells: 109 nCPM
- macrophages: 41 nCPM
- cdc: 21 nCPM
- pericytes: 8.2 nCPM
- fibroblasts: 4.4 nCPM
- decidual stromal cells: 3.9 nCPM
Immune cell
- classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 0.9 nTPM
- choroid plexus: 0.1 nTPM
- hippocampal formation: 0.1 nTPM
- hypothalamus: 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)
- 1.75
- gnomAD pLI
- 0.04
- gnomAD missense Z
- 0.1
- DepMap mean gene effect
- -0.08
- 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
- antimicrobial humoral immune response mediated by antimicrobial peptide
- cell-cell signaling
- chemokine-mediated signaling pathway
- chemotaxis
- cytoskeleton organization
- eosinophil chemotaxis
- inflammatory response
- intracellular calcium ion homeostasis
- killing of cells of another organism
- positive regulation of cell migration
- regulation of cell shape
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CCL13 as an antibody target. Whether an autoantibody or antibody against CCL13 could matter depends on whether native CCL13 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCL13 is annotated as secreted, so native CCL13 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 CCL13 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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