Formyl peptide receptor 3

FPR3
Identifiers
Aliases	FPR3, FML2_HUMAN, FMLPY, FPRH1, FPRH2, FPRL2, RMLP-R-I, FMLP-R-II, formyl peptide receptor 3
External IDs	OMIM: 136539; HomoloGene: 130500; GeneCards: FPR3; OMA:FPR3 - orthologs
Gene location (Human)
Chr.	Chromosome 19 (human)
End	51,826,190 bp
RNA expression pattern
	Top expressed in
	gallbladder; ; rectum; ; gonad; ; amniotic fluid; ; right coronary artery; ; synovial joint; ; synovial membrane; ; mucosa of sigmoid colon; ; appendix; ; Achilles tendon;
	n/a
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	G protein-coupled receptor activity; signal transducer activity; complement receptor activity; N-formyl peptide receptor activity;
Cellular component	integral component of membrane; plasma membrane; membrane; integral component of plasma membrane;
Biological process	chemotaxis; signal transduction; complement receptor mediated signaling pathway; inflammatory response; phospholipase C-activating G protein-coupled receptor signaling pathway; positive regulation of cytosolic calcium ion concentration; leukocyte migration; cell chemotaxis; G protein-coupled receptor signaling pathway;
	Sources:Amigo / QuickGO
Orthologs
	2359
	n/a
	ENSG00000187474
	n/a
	P25089
	n/a
	NM_002030
	n/a
	NP_002021
	n/a
	Wikidata
View/Edit Human

N-formyl peptide receptor 3 (FPR3) is a receptor protein that in humans is encoded by the FPR3 gene.