Basic Information

FPR1

Full name: formyl peptide receptor 1

Gene type: protein coding

HGNC ID: HGNC:3826

Gene location: 19q13.41

Gene resources

NCBI: https://www.ncbi.nlm.nih.gov/gene/2357

Alliance of genome: https://www.alliancegenome.org/gene/HGNC:3826

MANE select: https://www.ncbi.nlm.nih.gov/gene/?term=NM_002029.4

Protein resources

UniProt/Swiss-Prot: https://www.uniprot.org/uniprot/P21462

AlphaFold: https://alphafold.ebi.ac.uk/entry/P21462

MEME motif:

Clinical resources

OMIM: https://www.omim.org/entry/136537

dbVar: https://www.ncbi.nlm.nih.gov/dbvar?LinkName=gene_dbvar&from_uid=2357

Pathway resources

KEGG pathway: https://www.genome.jp/pathway/hsa04015+2357

Variant resources

Gene Disease type Variant type NCBI dbSNP Alleles Variant location
FPR1 AMD Intron Variant rs7253284 A>C / A>G chr19:51747508 (GRCh38.p13)
FPR1 AMD Intron Variant rs7253355 G>A / G>C chr19:51747336 (GRCh38.p13)
FPR1 rs5030878 chr19:51746963 (GRCh38.p13)
FPR1 AMD Missense Variant rs78488639 G>A / G>T chr19:51746706 (GRCh38.p13)
FPR1 AMD Missense Variant rs2070745 C>G / C>T chr19:51746694 (GRCh38.p13)
FPR1 AMD Synonymous Variant rs28930680 A>G chr19:51746689 (GRCh38.p13)
FPR1 AMD Synonymous Variant rs5030879 G>A chr19:51746647 (GRCh38.p13)
FPR1 AMD Synonymous Variant rs2070746 G>A / G>T chr19:51746449 (GRCh38.p13)
FPR1 AMD Missense Variant rs5030880 T>A chr19:51746427 (GRCh38.p13)
FPR1 AMD Missense Variant rs867228 T>A / T>C / T>G
FPR1 AMD 3 Prime UTR Variant rs867341 T>C chr19:51745867 (GRCh38.p13)
FPR1 AMD 3 Prime UTR Variant rs867229 G>A / G>T chr19:51745746 (GRCh38.p13)
FPR1 AMD 3 Prime UTR Variant rs1868943 A>G / A>T chr19:51745737 (GRCh38.p13)
FPR1 PCV rs5030878