Gene Gene information from NCBI Gene database.
Entrez ID 2358
Gene name Formyl peptide receptor 2
Gene symbol FPR2
Synonyms (NCBI Gene)
ALXALXRFMLP-R-IIFMLPXFPR2AFPRH1FPRH2FPRL1HM63LXA4R
Chromosome 19
Chromosome location 19q13.41
miRNA miRNA information provided by mirtarbase database.
249
miRTarBase ID miRNA Experiments Reference
MIRT619736 hsa-miR-125a-3p HITS-CLIP 23824327
MIRT619735 hsa-miR-764 HITS-CLIP 23824327
MIRT619734 hsa-miR-3934-5p HITS-CLIP 23824327
MIRT619733 hsa-miR-5088-3p HITS-CLIP 23824327
MIRT619732 hsa-miR-1248 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
71
GO ID Ontology Definition Evidence Reference
GO:0001540 Function Amyloid-beta binding IPI 11316806
GO:0001540 Function Amyloid-beta binding ISS
GO:0001774 Process Microglial cell activation IEA
GO:0001774 Process Microglial cell activation ISS
GO:0002430 Process Complement receptor mediated signaling pathway IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
136538 3827 ENSG00000171049
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P25090
Protein name N-formyl peptide receptor 2 (FMLP-related receptor I) (FMLP-R-I) (Formyl peptide receptor-like 1) (HM63) (Lipoxin A4 receptor) (LXA4 receptor) (RFP)
Protein function Low affinity receptor for N-formyl-methionyl peptides, which are powerful neutrophil chemotactic factors (PubMed:1374236). Binding of FMLP to the receptor causes activation of neutrophils (PubMed:1374236). This response is mediated via a G-prote
PDB 6LW5 , 6OMM , 7T6S , 7T6U , 7T6V , 7WVV , 7WVW , 7WVX , 7WVY , 8Y62 , 8Y63
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00001 7tm_1 43 302 7 transmembrane receptor (rhodopsin family) Family
Tissue specificity TISSUE SPECIFICITY: Detected in lung, bone marrow, neutrophils, spleen and testis. {ECO:0000269|PubMed:15465011, ECO:0000269|PubMed:9151906}.
Sequence
Sequence length 351
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Neuroactive ligand-receptor interaction
Neutrophil extracellular trap formation
Staphylococcus aureus infection
  G alpha (q) signalling events
G alpha (i) signalling events
Formyl peptide receptors bind formyl peptides and many other ligands
Neutrophil degranulation
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
CROHN DISEASE CTD
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CROHNS DISEASE OF LARGE BOWEL Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Lung adenocarcinoma Uncertain significance ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Alzheimer Disease Alzheimer disease Pubtator 16212921, 20141570, 33804025, 33811735 Associate
★☆☆☆☆
Found in Text Mining only
Amyotrophic Lateral Sclerosis Amyotrophic Lateral Sclerosis BEFREE 26107889
★☆☆☆☆
Found in Text Mining only
Anemia, Diamond-Blackfan Anemia BEFREE 15771965
★☆☆☆☆
Found in Text Mining only
Arrhythmogenic Right Ventricular Dysplasia Arrhythmogenic right ventricular cardiomyopathy Pubtator 30664203 Associate
★☆☆☆☆
Found in Text Mining only
Arteriosclerosis Arteriosclerosis BEFREE 19167353, 23500463, 25341894, 28071789
★☆☆☆☆
Found in Text Mining only
Arthritis Arthritis BEFREE 15171815, 15188355
★☆☆☆☆
Found in Text Mining only
Arthritis Arthritis Pubtator 15171815, 15188355 Associate
★☆☆☆☆
Found in Text Mining only
Arthritis Arthritis LHGDN 15188355
★☆☆☆☆
Found in Text Mining only
Arthritis Rheumatoid Rheumatoid arthritis Pubtator 15188355, 28316377 Associate
★☆☆☆☆
Found in Text Mining only
Asthma Asthma LHGDN 18583575
★☆☆☆☆
Found in Text Mining only