CCR9
C-C chemokine receptor type 9
Also known as: CCR9_HUMAN, CDw199, GPR-9-6, GPR28
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P51686
- Gene
- CCR9
- Ensembl
- ENSG00000173585
- Chromosome
- 3
- Canonical length
- 369 aa
- Protein class
- CD markers, G-protein coupled receptors, Predicted intracellular proteins, Predicted membrane proteins
- Subcellular location
- Endoplasmic reticulum,Plasma membrane
OverviewNCBI Gene
The protein encoded by this gene is a G protein-coupled receptor with seven transmembrane domains that belongs to the beta chemokine receptor family. Chemokines and their receptors are key regulators of thymocyte migration and maturation in normal and inflammation conditions. This gene is differentially expressed in T lymphocytes of the small intestine and colon, and its interaction with chemokine 25 contributes to intestinal intra-epithelial lymphocyte homing to the small intestine. This suggests a role for this gene in directing immune responses to different segments of the gastrointestinal tract. This gene and its exclusive ligand, chemokine 25, are overexpressed in a variety of malignant tumors and are closely associated with tumor proliferation, apoptosis, invasion, migration and drug resistance. This gene maps to the chemokine receptor gene cluster. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2020]
Canonical amino-acid sequenceUniProt
369 residues, UniProt reviewed canonical sequence.
>P51686|CCR9
1 MTPTDFTSPI PNMADDYGSE STSSMEDYVN FNFTDFYCEK NNVRQFASHF LPPLYWLVFI
61 VGALGNSLVI LVYWYCTRVK TMTDMFLLNL AIADLLFLVT LPFWAIAAAD QWKFQTFMCK
121 VVNSMYKMNF YSCVLLIMCI SVDRYIAIAQ AMRAHTWREK RLLYSKMVCF TIWVLAAALC
181 IPEILYSQIK EESGIAICTM VYPSDESTKL KSAVLTLKVI LGFFLPFVVM ACCYTIIIHT
241 LIQAKKSSKH KALKVTITVL TVFVLSQFPY NCILLVQTID AYAMFISNCA VSTNIDICFQ
301 VTQTIAFFHS CLNPVLYVFV GERFRRDLVK TLKNLGCISQ AQWVSFTRRE GSLKLSSMLL
361 ETTSGALSLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCR9 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
- Cell surface
- Secreted
- No
- Transmembrane segments
- 7
- Mean surface accessibility (rSASA)
- 0.32
- Highest tissue expression
- 121 nTPM
Expression across tissuesHPA
Tissue
- thymus: 121 nTPM
- small intestine: 5.3 nTPM
- duodenum: 3.7 nTPM
- appendix: 1 nTPM
- spleen: 1 nTPM
- choroid plexus: 0.9 nTPM
Single-cell type
- thymocytes: 31 nCPM
- cardiomyocytes: 18 nCPM
- nk-cells: 17 nCPM
- epicardial cells: 9.1 nCPM
- myonuclei: 8.8 nCPM
- innate lymphoid cells: 8.3 nCPM
Immune cell
- memory B-cell: 24 nTPM
- naive B-cell: 16 nTPM
- T-reg: 8.2 nTPM
- memory CD4 T-cell: 2.8 nTPM
- total PBMC: 2.7 nTPM
- memory CD8 T-cell: 2.4 nTPM
Brain region
- choroid plexus: 1.5 nTPM
- medulla oblongata: 1.3 nTPM
- basal ganglia: 1 nTPM
- cerebral cortex: 1 nTPM
- pons: 1 nTPM
- spinal cord: 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)
- 1.13
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.96
- DepMap mean gene effect
- 0.14
- DepMap dependency class
- none
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
- calcium-mediated signaling
- CD8-positive, gamma-delta intraepithelial T cell differentiation
- cell chemotaxis
- cellular defense response
- chemotaxis
- G protein-coupled receptor signaling pathway
- immune response
- positive regulation of cytosolic calcium ion concentration
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CCR9 as an antibody target. Whether an autoantibody or antibody against CCR9 could matter depends on whether native CCR9 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCR9 is annotated at the cell surface, where native CCR9 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.
Annotation status
The present source text does not explicitly label CCR9 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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