XCR1
Chemokine XC receptor 1
Also known as: CCXCR1, GPR5, XCR1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P46094
- Gene
- XCR1
- Ensembl
- ENSG00000173578
- Chromosome
- 3
- Canonical length
- 333 aa
- Protein class
- G-protein coupled receptors, Human disease related genes, Predicted membrane proteins
OverviewNCBI Gene
The protein encoded by this gene is a chemokine receptor belonging to the G protein-coupled receptor superfamily. The family members are characterized by the presence of 7 transmembrane domains. The encoded protein transduces a signal by increasing the intracellular calcium ion level. The viral macrophage inflammatory protein-II is an antagonist of this receptor and blocks signaling. Some studies have implicated a cluster of genes at 3p21.31, including this gene, as associated with COVID-19 risk. The encoded protein may also play a role in cell proliferation and migration in several types of cancer. [provided by RefSeq, Jan 2023]
Canonical amino-acid sequenceUniProt
333 residues, UniProt reviewed canonical sequence.
>P46094|XCR1
1 MESSGNPEST TFFYYDLQSQ PCENQAWVFA TLATTVLYCL VFLLSLVGNS LVLWVLVKYE
61 SLESLTNIFI LNLCLSDLVF ACLLPVWISP YHWGWVLGDF LCKLLNMIFS ISLYSSIFFL
121 TIMTIHRYLS VVSPLSTLRV PTLRCRVLVT MAVWVASILS SILDTIFHKV LSSGCDYSEL
181 TWYLTSVYQH NLFFLLSLGI ILFCYVEILR TLFRSRSKRR HRTVKLIFAI VVAYFLSWGP
241 YNFTLFLQTL FRTQIIRSCE AKQQLEYALL ICRNLAFSHC CFNPVLYVFV GVKFRTHLKH
301 VLRQFWFCRL QAPSPASIPH SPGAFAYEGA SFYLocalizationUniProt · AlphaFold · HPA
Whether an antibody against XCR1 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)
- 0.33
- Highest tissue expression
- 8.2 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 8.2 nTPM
- thymus: 5.7 nTPM
- spleen: 5.1 nTPM
- tonsil: 3.5 nTPM
- placenta: 2.7 nTPM
- appendix: 2.5 nTPM
Single-cell type
- myonuclei: 237 nCPM
- cdc: 30 nCPM
- extravillous trophoblasts: 25 nCPM
- migrating cytotrophoblasts: 23 nCPM
- pdcs: 17 nCPM
- plasma cells: 7.3 nCPM
Immune cell
- myeloid DC: 2.3 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- thalamus: 0.6 nTPM
- cerebral cortex: 0.2 nTPM
- medulla oblongata: 0.2 nTPM
- midbrain: 0.2 nTPM
- amygdala: 0.1 nTPM
- basal ganglia: 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)
- 1.08
- gnomAD pLI
- 0.02
- gnomAD missense Z
- 1.12
- DepMap mean gene effect
- 0.04
- 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
- cell chemotaxis
- chemotaxis
- G protein-coupled receptor signaling pathway
- G protein-coupled receptor signaling pathway, coupled to cyclic nucleotide second messenger
- immune response
- inflammatory response
- positive regulation of cytosolic calcium ion concentration
- release of sequestered calcium ion into cytosol
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads XCR1 as an antibody target. Whether an autoantibody or antibody against XCR1 could matter depends on whether native XCR1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
XCR1 is annotated at the cell surface, where native XCR1 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 XCR1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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