FFAR2
Free fatty acid receptor 2
Also known as: FFA2R, FFAR2_HUMAN, GPR43
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O15552
- Gene
- FFAR2
- Ensembl
- ENSG00000126262
- Chromosome
- 19
- Canonical length
- 330 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
This gene encodes a member of the GP40 family of G protein-coupled receptors that are clustered together on chromosome 19. The encoded protein is a receptor for short chain free fatty acids and may be involved in the inflammatory response and in regulating lipid plasma levels. [provided by RefSeq, Apr 2009]
Canonical amino-acid sequenceUniProt
330 residues, UniProt reviewed canonical sequence.
>O15552|FFAR2
1 MLPDWKSSLI LMAYIIIFLT GLPANLLALR AFVGRIRQPQ PAPVHILLLS LTLADLLLLL
61 LLPFKIIEAA SNFRWYLPKV VCALTSFGFY SSIYCSTWLL AGISIERYLG VAFPVQYKLS
121 RRPLYGVIAA LVAWVMSFGH CTIVIIVQYL NTTEQVRSGN EITCYENFTD NQLDVVLPVR
181 LELCLVLFFI PMAVTIFCYW RFVWIMLSQP LVGAQRRRRA VGLAVVTLLN FLVCFGPYNV
241 SHLVGYHQRK SPWWRSIAVV FSSLNASLDP LLFYFSSSVV RRAFGRGLQV LRNQGSSLLG
301 RRGKDTAEGT NEDRGVGQGE GMPSSDFTTELocalizationUniProt · AlphaFold · HPA
Whether an antibody against FFAR2 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)
- 0.3
- Highest tissue expression
- 21 nTPM
Expression across tissuesHPA
Tissue
- spleen: 21 nTPM
- bone marrow: 19 nTPM
- appendix: 17 nTPM
- lung: 7.3 nTPM
- urinary bladder: 5.6 nTPM
- adipose tissue: 4.6 nTPM
Single-cell type
- neutrophils: 314 nCPM
- monocytes: 41 nCPM
- neuroendocrine cells: 32 nCPM
- kupffer cells: 27 nCPM
- monocyte progenitors: 18 nCPM
- goblet cells: 15 nCPM
Immune cell
- neutrophil: 250 nTPM
- eosinophil: 85 nTPM
- non-classical monocyte: 6.5 nTPM
- intermediate monocyte: 5.6 nTPM
- basophil: 3.1 nTPM
- classical monocyte: 2.1 nTPM
Brain region
- white matter: 2.6 nTPM
- choroid plexus: 2 nTPM
- cerebral cortex: 1.9 nTPM
- medulla oblongata: 1.9 nTPM
- basal ganglia: 1.8 nTPM
- thalamus: 1.8 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)
- 1.26
- gnomAD pLI
- 0.01
- gnomAD missense Z
- 0.12
- DepMap mean gene effect
- -0.17
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 0% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- cell surface pattern recognition receptor signaling pathway
- cellular response to fatty acid
- fat cell differentiation
- G protein-coupled receptor signaling pathway
- glucose homeostasis
- leukocyte chemotaxis involved in inflammatory response
- ligand-gated ion channel signaling pathway
- lipid storage
- mucosal immune response
- negative regulation of insulin secretion
- phospholipase C-activating G protein-coupled receptor signaling pathway
- positive regulation of acute inflammatory response to non-antigenic stimulus
- positive regulation of chemokine production
- positive regulation of cytokine production involved in immune response
- positive regulation of insulin secretion
- positive regulation of interleukin-8 production
- regulation of acute inflammatory response
- regulation of peptide hormone secretion
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of FFAR2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FFAR2 as an antibody target. Whether an autoantibody or antibody against FFAR2 could matter depends on whether native FFAR2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FFAR2 is annotated at the cell surface, where native FFAR2 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 FFAR2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...