CCL1
C-C motif chemokine 1
Also known as: CCL1_HUMAN, I-309, P500, SCYA1, SISe, TCA3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P22362
- Gene
- CCL1
- Ensembl
- ENSG00000108702
- Chromosome
- 17
- Canonical length
- 96 aa
- Protein class
- Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
This antimicrobial gene is one of several chemokine genes clustered on the q-arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N-terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, is secreted by activated T cells and displays chemotactic activity for monocytes but not for neutrophils. It binds to the chemokine (C-C motif) receptor 8. [provided by RefSeq, Sep 2014]
Canonical amino-acid sequenceUniProt
96 residues, UniProt reviewed canonical sequence.
>P22362|CCL1
1 MQIITTALVC LLLAGMWPED VDSKSMQVPF SRCCFSFAEQ EIPLRAILCY RNTSSICSNE
61 GLIFKLKRGK EACALDTVGW VQRHRKMLRH CPSKRKLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCL1 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
- 2.1 nTPM
Expression across tissuesHPA
Tissue
- rectum: 2.1 nTPM
- thymus: 1.1 nTPM
- testis: 0.3 nTPM
- basal ganglia: 0.2 nTPM
- cerebral cortex: 0.2 nTPM
- colon: 0.2 nTPM
Single-cell type
- early spermatids: 3.2 nCPM
- t-cells: 2.6 nCPM
- late spermatids: 2.5 nCPM
- thymocytes: 1.7 nCPM
- basal keratinocytes: 0.3 nCPM
- plasma cells: 0.3 nCPM
Immune cell
- classical monocyte: 0.3 nTPM
- intermediate monocyte: 0.2 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- cerebral cortex: 1.1 nTPM
- white matter: 0.3 nTPM
- hippocampal formation: 0.2 nTPM
- hypothalamus: 0.2 nTPM
- midbrain: 0.2 nTPM
- amygdala: 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)
- 1.82
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.25
- DepMap mean gene effect
- -0.15
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% 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
- chemokine-mediated signaling pathway
- chemotaxis
- eosinophil chemotaxis
- inflammatory response
- intracellular calcium ion homeostasis
- positive regulation of cell migration
- positive regulation of cytosolic calcium ion concentration
- positive regulation of inflammatory response
- positive regulation of interleukin-17 production
- positive regulation of monocyte chemotaxis
- signal transduction
- viral process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CCL1 as an antibody target. Whether an autoantibody or antibody against CCL1 could matter depends on whether native CCL1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCL1 is annotated as secreted, so native CCL1 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 CCL1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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