PTGIR prostaglandin I2 receptor
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
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MGeND data only
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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 | |||||||||||
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MGeND data only
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| 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
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| 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 | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | PRIPR |
| SYNONYM | IP |
| MIM | 600022 OMIM |
| HGNC | HGNC:9602 HGNC |
| Ensembl | ENSG00000160013 Ensembl |
| AllianceGenome | HGNC:9602 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| 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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