PTGER3 prostaglandin E receptor 3
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 4 |
| not provided | 2 | 0 |
| Uncertain significance | 0 | 28 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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34 |
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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
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| Target data | : |
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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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| 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 | EP3 |
| SYNONYM | EP3-I |
| SYNONYM | EP3-II |
| SYNONYM | EP3-III |
| SYNONYM | EP3-IV |
| SYNONYM | EP3-VI |
| SYNONYM | EP3e |
| SYNONYM | PGE2-R |
| SYNONYM | lnc003875 |
| MIM | 176806 OMIM |
| HGNC | HGNC:9595 HGNC |
| Ensembl | ENSG00000050628 Ensembl |
| AllianceGenome | HGNC:9595 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000460330.5 | hg38 | chr1 | 70,852,573 | 71,047,633 | 195,061 |
| ENST00000306666.10 | hg38 | chr1 | 70,970,782 | 71,047,816 | 77,035 |
| ENST00000356595.8 | hg38 | chr1 | 70,952,432 | 71,047,788 | 95,357 |
| ENST00000370931.7 | hg38 | chr1 | 70,852,353 | 71,047,788 | 195,436 |
| ENST00000628037.2 | hg38 | chr1 | 70,852,353 | 71,047,808 | 195,456 |
| ENST00000370924.5 | hg38 | chr1 | 71,005,854 | 71,047,808 | 41,955 |
| ENST00000370931.7 | hg19 | chr1 | 71,318,036 | 71,513,471 | 195,436 |
| ENST00000628037.2 | hg19 | chr1 | 71,318,036 | 71,513,491 | 195,456 |
| ENST00000460330.5 | hg19 | chr1 | 71,318,256 | 71,513,316 | 195,061 |
| ENST00000356595.8 | hg19 | chr1 | 71,418,115 | 71,513,471 | 95,357 |
| ENST00000306666.10 | hg19 | chr1 | 71,436,465 | 71,513,499 | 77,035 |
| ENST00000370924.5 | hg19 | chr1 | 71,471,537 | 71,513,491 | 41,955 |
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