C5AR2
C5a anaphylatoxin chemotactic receptor 2
Also known as: C5AR2_HUMAN, C5L2, GPR77
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9P296
- Gene
- C5AR2
- Ensembl
- ENSG00000134830
- Chromosome
- 19
- Canonical length
- 337 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a G-protein coupled receptor 1 family member involved in the complement system of the innate immune response. Unlike classical G-protein coupled receptors, the encoded protein does not associate with intracellular G-proteins. It may instead modulate signal transduction through the beta-arrestin pathway, and may alternatively act as a decoy receptor. This gene may be involved in coronary artery disease and in the pathogenesis of sepsis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]
Canonical amino-acid sequenceUniProt
337 residues, UniProt reviewed canonical sequence.
>Q9P296|C5AR2
1 MGNDSVSYEY GDYSDLSDRP VDCLDGACLA IDPLRVAPLP LYAAIFLVGV PGNAMVAWVA
61 GKVARRRVGA TWLLHLAVAD LLCCLSLPIL AVPIARGGHW PYGAVGCRAL PSIILLTMYA
121 SVLLLAALSA DLCFLALGPA WWSTVQRACG VQVACGAAWT LALLLTVPSA IYRRLHQEHF
181 PARLQCVVDY GGSSSTENAV TAIRFLFGFL GPLVAVASCH SALLCWAARR CRPLGTAIVV
241 GFFVCWAPYH LLGLVLTVAA PNSALLARAL RAEPLIVGLA LAHSCLNPML FLYFGRAQLR
301 RSLPAACHWA LRESQGQDES VDSKKSTSHD LVSEMEVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against C5AR2 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)
- 0.34
- Highest tissue expression
- 13 nTPM
Expression across tissuesHPA
Tissue
- spleen: 13 nTPM
- lung: 6.1 nTPM
- bone marrow: 5.5 nTPM
- adipose tissue: 3.9 nTPM
- appendix: 3.9 nTPM
- tonsil: 3 nTPM
Single-cell type
- neutrophils: 241 nCPM
- kupffer cells: 150 nCPM
- monocytes: 139 nCPM
- macrophages: 84 nCPM
- neutrophil progenitors: 56 nCPM
- cdc: 35 nCPM
Immune cell
- neutrophil: 33 nTPM
- basophil: 18 nTPM
- eosinophil: 12 nTPM
- non-classical monocyte: 4.4 nTPM
- classical monocyte: 2.7 nTPM
- intermediate monocyte: 2.3 nTPM
Brain region
- cerebral cortex: 11 nTPM
- hippocampal formation: 9.2 nTPM
- choroid plexus: 8 nTPM
- medulla oblongata: 7 nTPM
- white matter: 6.8 nTPM
- cerebellum: 6.6 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
- 0.25
- gnomAD missense Z
- -0.15
- DepMap mean gene effect
- 0.04
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- chemotaxis
- complement receptor mediated signaling pathway
- inflammatory response
- negative regulation of interleukin-6 production
- negative regulation of neutrophil chemotaxis
- negative regulation of tumor necrosis factor production
- phospholipase C-activating G protein-coupled receptor signaling pathway
- positive regulation of cytosolic calcium ion concentration
- regulation of interleukin-8 production
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads C5AR2 as an antibody target. Whether an autoantibody or antibody against C5AR2 could matter depends on whether native C5AR2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
C5AR2 is annotated at the cell surface, where native C5AR2 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 C5AR2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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