FPR1 formyl peptide receptor 1

Information
Symbol
FPR1
Type
protein-coding
Description
formyl peptide receptor 1
Entrez Gene ID
2357
Genome
hg19
Position
chr19:52,248,425-52,255,146
Genome
hg38
Position
chr19:51,745,172-51,751,893
MIM
136537 OMIM
HGNC
HGNC:3826 HGNC
Ensembl
ENSG00000171051 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 38
Likely benign 0 150
Conflicting classifications of pathogenicity 0 2
not provided 8 0
Uncertain significance 0 282
Ranking
ClinVar
0
0
50
412
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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Variant name Gene AA change CDS Japanese
frequency
TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence
Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM FMLP
SYNONYM FPR
MIM 136537 OMIM
HGNC HGNC:3826 HGNC
Ensembl ENSG00000171051 Ensembl
AllianceGenome HGNC:3826
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000595042.5 hg38 chr19 51,745,172 51,751,893 6,722
ENST00000594900.2 hg38 chr19 51,745,773 51,804,115 58,343
ENST00000600815.2 hg38 chr19 51,745,773 51,750,811 5,039
ENST00000304748.5 hg38 chr19 51,745,773 51,751,878 6,106
ENST00000595042.5 hg19 chr19 52,248,425 52,255,146 6,722
ENST00000600815.2 hg19 chr19 52,249,026 52,254,064 5,039
ENST00000304748.5 hg19 chr19 52,249,026 52,255,131 6,106
ENST00000594900.2 hg19 chr19 52,249,026 52,307,368 58,343
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