CXCL3
C-X-C motif chemokine 3
Also known as: CINC-2b, CXCL3_HUMAN, GRO3, GROg, MIP-2b, SCYB3
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P19876
- Gene
- CXCL3
- Ensembl
- ENSG00000163734
- Chromosome
- 4
- Canonical length
- 107 aa
- Protein class
- Plasma proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
OverviewNCBI Gene
This antimicrobial gene encodes a member of the CXC subfamily of chemokines. The encoded protein is a secreted growth factor that signals through the G-protein coupled receptor, CXC receptor 2. This protein plays a role in inflammation and as a chemoattractant for neutrophils. [provided by RefSeq, Sep 2014]
Canonical amino-acid sequenceUniProt
107 residues, UniProt reviewed canonical sequence.
>P19876|CXCL3
1 MAHATLSAAP SNPRLLRVAL LLLLLVAASR RAAGASVVTE LRCQCLQTLQ GIHLKNIQSV
61 NVRSPGPHCA QTEVIATLKN GKKACLNPAS PMVQKIIEKI LNKGSTNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CXCL3 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)
- 0.48
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 20 nTPM
- cervix: 19 nTPM
- lung: 17 nTPM
- bone marrow: 15 nTPM
- urinary bladder: 15 nTPM
- appendix: 14 nTPM
Single-cell type
- monocytes: 1,378 nCPM
- epididymal basal cells: 1,167 nCPM
- cdc: 807 nCPM
- macrophages: 638 nCPM
- endometrial secretory cells: 474 nCPM
- epididymal efferent duct absorptive cells: 468 nCPM
Immune cell
- total PBMC: 0.4 nTPM
- intermediate monocyte: 0.1 nTPM
- non-classical monocyte: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- thalamus: 5 nTPM
- cerebral cortex: 4 nTPM
- amygdala: 0.7 nTPM
- hypothalamus: 0.6 nTPM
- white matter: 0.6 nTPM
- choroid plexus: 0.5 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CXCL3.
Disease | ImmuneIEDB
Conditions an epitope on CXCL3 was assayed in.
- type 1 diabetes mellitus T cell
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)
- 1.85
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.72
- DepMap mean gene effect
- 0.02
- 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
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CXCL3 as an antibody target. Whether an autoantibody or antibody against CXCL3 could matter depends on whether native CXCL3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CXCL3 is annotated as secreted, so native CXCL3 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 CXCL3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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