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Gene: Fpr-rs3 (formyl peptide receptor, related sequence 3) Mus musculus
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Symbol: Fpr-rs3
Name: formyl peptide receptor, related sequence 3
CRRD ID: 1319147
Description: Exhibits N-formyl peptide receptor activity. Predicted to be involved in several processes, including complement receptor mediated signaling pathway; phospholipase C-activating G protein-coupled receptor signaling pathway; and positive regulation of cytosolic calcium ion concentration. Predicted to localize to plasma membrane. Is expressed in accessory olfactory bulb; accessory olfactory bulb glomerular layer; and vomeronasal organ. Orthologous to human FPR2 (formyl peptide receptor 2) and FPR3 (formyl peptide receptor 3); INTERACTS WITH 3,4-methylenedioxymethamphetamine.
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: formyl peptide receptor-related sequence 3; N-formylpeptide receptor-like 3
Orthologs:
No known orthologs. homologs ...
Related Pseudogenes: Fpr-rs5  
Latest Assembly: GRCm38 - Mouse Genome Assembly GRCm38
Position:
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391720,844,108 - 20,845,139 (-)NCBI
GRCm381720,623,846 - 20,624,877 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1720,623,846 - 20,624,877 (-)EnsemblGRCm38mm10GRCm38
MGSCv371720,760,810 - 20,761,841 (-)NCBIGRCm37mm9NCBIm37
MGSCv361720,328,543 - 20,329,574 (-)NCBImm8
Celera1721,666,410 - 21,667,441 (-)NCBICelera
Cytogenetic Map17A3.2NCBI
JBrowse: View Region in Genome Browser (JBrowse)
Model


References - curated
References - uncurated

Genomics

Position Markers
QTLs in Region (GRCm38)
miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences

Additional Information

External Database Links
 
More on Fpr-rs3
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: mm9 mm10
MGI Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1319147
Created: 2005-01-12
Species: Mus musculus
Last Modified: 2020-10-13
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.