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Gene : FPR1 Homo sapiens

Name  ? formyl peptide receptor 1 Cytological Location  19q13.41
Brief Description  formyl peptide receptor 1
Description  This gene encodes a G protein-coupled receptor of mammalian phagocytic cells that is a member of the G-protein coupled receptor 1 family. The protein mediates the response of phagocytic cells to invasion of the host by microorganisms and is important in host defense and inflammation.[provided by RefSeq, Jul 2010]
  • synonyms:
  • M60627,
  • OTTHUMG00000183500,
  • NM_002029,
  • FMLP,
  • FMLP,
  • FPR1,
  • uc002pxq.4,
  • HGNC:3826,
  • FPR,
  • FPR
  • identifiers:
  • 2357,
  • ENSG00000171051,
  • FPR1

Genome feature

Region: gene ? Length: 6707  
Location: 19:51745172-51751878 reverse strand Cyto location: 19q13.41

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Proteins.


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0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



619 SN Ps

5 Cross References

18 Data Sets

7 Homologues

0 Located Features

97 Rna Seq Results