PTGIR prostaglandin I2 receptor

Information
Symbol
PTGIR
Type
protein-coding
Description
prostaglandin I2 receptor
Entrez Gene ID
5739
Genome
hg19
Position
chr19:47,123,725-47,128,346
Genome
hg38
Position
chr19:46,620,468-46,625,089
MIM
600022 OMIM
HGNC
HGNC:9602 HGNC
Ensembl
ENSG00000160013 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 6
Uncertain significance 0 54
Ranking
ClinVar
0
0
0
64
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
[No Data.]
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 PRIPR
SYNONYM IP
MIM 600022 OMIM
HGNC HGNC:9602 HGNC
Ensembl ENSG00000160013 Ensembl
AllianceGenome HGNC:9602
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000598865.5 hg38 chr19 46,621,167 46,625,072 3,906
ENST00000597185.1 hg38 chr19 46,621,167 46,625,072 3,906
ENST00000594275.1 hg38 chr19 46,621,167 46,625,072 3,906
ENST00000596260.1 hg38 chr19 46,623,130 46,625,037 1,908
ENST00000291294.7 hg38 chr19 46,620,468 46,625,089 4,622
ENST00000291294.7 hg19 chr19 47,123,725 47,128,346 4,622
ENST00000594275.1 hg19 chr19 47,124,424 47,128,329 3,906
ENST00000597185.1 hg19 chr19 47,124,424 47,128,329 3,906
ENST00000598865.5 hg19 chr19 47,124,424 47,128,329 3,906
ENST00000596260.1 hg19 chr19 47,126,387 47,128,294 1,908
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