CCR10
C-C chemokine receptor type 10
Also known as: CCR10_HUMAN, GPR2
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P46092
- Gene
- CCR10
- Ensembl
- ENSG00000184451
- Chromosome
- 17
- Canonical length
- 362 aa
- Protein class
- Cancer-related genes, G-protein coupled receptors, Plasma proteins, Predicted membrane proteins
- Subcellular location
- Endoplasmic reticulum
OverviewNCBI Gene
Chemokines are a group of small (approximately 8 to 14 kD), mostly basic, structurally related molecules that regulate cell trafficking of various types of leukocytes through interactions with a subset of 7-transmembrane, G protein-coupled receptors. Chemokines also play fundamental roles in the development, homeostasis, and function of the immune system, and they have effects on cells of the central nervous system as well as on endothelial cells involved in angiogenesis or angiostasis. Chemokines are divided into 2 major subfamilies, CXC and CC, based on the arrangement of the first 2 of the 4 conserved cysteine residues; the 2 cysteines are separated by a single amino acid in CXC chemokines and are adjacent in CC chemokines. CCR10 is the receptor for CCL27 (SCYA27; MIM 604833); CCR10-CCL27 interactions are involved in T cell-mediated skin inflammation (Homey et al., 2002 [PubMed 11821900]).[supplied by OMIM, Mar 2008]
Canonical amino-acid sequenceUniProt
362 residues, UniProt reviewed canonical sequence.
>P46092|CCR10
1 MGTEATEQVS WGHYSGDEED AYSAEPLPEL CYKADVQAFS RAFQPSVSLT VAALGLAGNG
61 LVLATHLAAR RAARSPTSAH LLQLALADLL LALTLPFAAA GALQGWSLGS ATCRTISGLY
121 SASFHAGFLF LACISADRYV AIARALPAGP RPSTPGRAHL VSVIVWLLSL LLALPALLFS
181 QDGQREGQRR CRLIFPEGLT QTVKGASAVA QVALGFALPL GVMVACYALL GRTLLAARGP
241 ERRRALRVVV ALVAAFVVLQ LPYSLALLLD TADLLAARER SCPASKRKDV ALLVTSGLAL
301 ARCGLNPVLY AFLGLRFRQD LRRLLRGGSC PSGPQPRRGC PRRPRLSSCS APTETHSLSW
361 DNLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CCR10 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)
- 0.36
- Highest tissue expression
- 20 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 20 nTPM
- cerebellum: 9.8 nTPM
- endometrium: 8.8 nTPM
- hypothalamus: 7.2 nTPM
- fallopian tube: 7.1 nTPM
- cervix: 6.9 nTPM
Single-cell type
- plasma cells: 107 nCPM
- cardiomyocytes: 81 nCPM
- epicardial cells: 61 nCPM
- pericytes: 37 nCPM
- epididymal principal cells: 30 nCPM
- vascular smooth muscle cells: 17 nCPM
Immune cell
- T-reg: 73 nTPM
- plasmacytoid DC: 25 nTPM
- memory CD4 T-cell: 11 nTPM
- naive B-cell: 5.9 nTPM
- memory CD8 T-cell: 5.4 nTPM
- memory B-cell: 5.3 nTPM
Brain region
- pons: 20 nTPM
- hypothalamus: 19 nTPM
- midbrain: 16 nTPM
- medulla oblongata: 14 nTPM
- cerebral cortex: 13 nTPM
- cerebellum: 12 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)
- 1.36
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.89
- DepMap mean gene effect
- -0.09
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- calcium-mediated signaling
- cell 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 CCR10 as an antibody target. Whether an autoantibody or antibody against CCR10 could matter depends on whether native CCR10 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CCR10 is annotated at the cell surface, where native CCR10 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 CCR10 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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