PAEP progestagen associated endometrial protein
Information
- Symbol
- PAEP
- Type
- protein-coding
- Description
- progestagen associated endometrial protein
- Entrez Gene ID
- 5047
- Genome
- hg19
- Position
- chr9:138,453,602-138,458,801
- Genome
- hg38
- Position
- chr9:135,561,756-135,566,955
- MIM
- 173310 OMIM
- HGNC
- HGNC:8573 HGNC
- Ensembl
- ENSG00000122133 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 6 |
| Likely benign | 0 | 8 |
| Uncertain significance | 0 | 20 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
34 |
 |
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
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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
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| 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
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| Category | : |
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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 | GD |
| SYNONYM | GdA |
| SYNONYM | GdF |
| SYNONYM | GdS |
| SYNONYM | PAEG |
| SYNONYM | PEP |
| SYNONYM | PP14 |
| SYNONYM | ZIF-1 |
| MIM | 173310 OMIM |
| HGNC | HGNC:8573 HGNC |
| Ensembl | ENSG00000122133 Ensembl |
| AllianceGenome | HGNC:8573 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000479141.6 | hg38 | chr9 | 135,561,756 | 135,566,955 | 5,200 |
| ENST00000371766.6 | hg38 | chr9 | 135,561,767 | 135,566,776 | 5,010 |
| ENST00000277508.9 | hg38 | chr9 | 135,561,777 | 135,566,776 | 5,000 |
| ENST00000611414.4 | hg38 | chr9 | 135,561,758 | 135,566,776 | 5,019 |
| ENST00000479141.6 | hg19 | chr9 | 138,453,602 | 138,458,801 | 5,200 |
| ENST00000611414.4 | hg19 | chr9 | 138,453,604 | 138,458,622 | 5,019 |
| ENST00000371766.6 | hg19 | chr9 | 138,453,613 | 138,458,622 | 5,010 |
| ENST00000277508.9 | hg19 | chr9 | 138,453,623 | 138,458,622 | 5,000 |
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