FFAR3
Free fatty acid receptor 3
Also known as: FFA3R, FFAR3_HUMAN, GPR41
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O14843
- Gene
- FFAR3
- Ensembl
- ENSG00000185897
- Chromosome
- 19
- Canonical length
- 346 aa
- Protein class
- G-protein coupled receptors, Predicted membrane proteins
OverviewNCBI Gene
Enables G protein-coupled receptor activity. Involved in adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway and cellular response to fatty acid. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
346 residues, UniProt reviewed canonical sequence.
>O14843|FFAR3
1 MDTGPDQSYF SGNHWFVFSV YLLTFLVGLP LNLLALVVFV GKLQRRPVAV DVLLLNLTAS
61 DLLLLLFLPF RMVEAANGMH WPLPFILCPL SGFIFFTTIY LTALFLAAVS IERFLSVAHP
121 LWYKTRPRLG QAGLVSVACW LLASAHCSVV YVIEFSGDIS HSQGTNGTCY LEFRKDQLAI
181 LLPVRLEMAV VLFVVPLIIT SYCYSRLVWI LGRGGSHRRQ RRVAGLLAAT LLNFLVCFGP
241 YNVSHVVGYI CGESPAWRIY VTLLSTLNSC VDPFVYYFSS SGFQADFHEL LRRLCGLWGQ
301 WQQESSMELK EQKGGEEQRA DRPAERKTSE HSQGCGTGGQ VACAESLocalizationUniProt · AlphaFold · HPA
Whether an antibody against FFAR3 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)
- 0.31
- Highest tissue expression
- 3.8 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 3.8 nTPM
- appendix: 2.4 nTPM
- breast: 2.2 nTPM
- smooth muscle: 1.5 nTPM
- colon: 1.2 nTPM
- spleen: 1.1 nTPM
Single-cell type
- mast cells: 8.8 nCPM
- monocytes: 4.9 nCPM
- innate lymphoid cells: 4.2 nCPM
- kupffer cells: 3.1 nCPM
- neutrophils: 2.5 nCPM
- pancreatic islet cells: 2.5 nCPM
Immune cell
- neutrophil: 2.8 nTPM
- eosinophil: 2.5 nTPM
- intermediate monocyte: 0.5 nTPM
- non-classical monocyte: 0.1 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
Brain region
- medulla oblongata: 2.1 nTPM
- white matter: 1.9 nTPM
- midbrain: 0.8 nTPM
- basal ganglia: 0.7 nTPM
- cerebral cortex: 0.7 nTPM
- choroid plexus: 0.7 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)
- 1.88
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.03
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
- adenylate cyclase-inhibiting G protein-coupled receptor signaling pathway
- cellular response to fatty acid
- G protein-coupled receptor signaling pathway
- inflammatory response
- mucosal immune response
- negative regulation of blood pressure
- positive regulation of acute inflammatory response to non-antigenic stimulus
- positive regulation of chemokine production
- positive regulation of cytokine production involved in immune response
- regulation of hormone biosynthetic process
- regulation of insulin receptor signaling pathway
- regulation of norepinephrine secretion
- regulation of peptide hormone secretion
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads FFAR3 as an antibody target. Whether an autoantibody or antibody against FFAR3 could matter depends on whether native FFAR3 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
FFAR3 is annotated at the cell surface, where native FFAR3 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 FFAR3 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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