FPR2 formyl peptide receptor 2

Information
Symbol
FPR2
Type
protein-coding
Description
formyl peptide receptor 2
Entrez Gene ID
2358
Genome
hg19
Position
chr19:52,266,013-52,273,760
Genome
hg38
Position
chr19:51,762,760-51,770,507
MIM
136538 OMIM
HGNC
HGNC:3827 HGNC
Ensembl
ENSG00000171049 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 2
Likely benign 0 4
not provided 1 0
Uncertain significance 0 42
Ranking
ClinVar
0
0
2
44
0
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 :
Search word :
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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 ALX
SYNONYM ALXR
SYNONYM FMLP-R-II
SYNONYM FMLPX
SYNONYM FPR2A
SYNONYM FPRH1
SYNONYM FPRH2
SYNONYM FPRL1
SYNONYM HM63
SYNONYM LXA4R
MIM 136538 OMIM
HGNC HGNC:3827 HGNC
Ensembl ENSG00000171049 Ensembl
AllianceGenome HGNC:3827
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000340023.7 hg38 chr19 51,761,180 51,770,531 9,352
ENST00000598776.1 hg38 chr19 51,762,760 51,770,507 7,748
ENST00000598953.1 hg38 chr19 51,761,212 51,770,013 8,802
ENST00000340023.7 hg19 chr19 52,264,433 52,273,784 9,352
ENST00000598953.1 hg19 chr19 52,264,465 52,273,266 8,802
ENST00000598776.1 hg19 chr19 52,266,013 52,273,760 7,748
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