Genomic Map
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Target Gene Details
Entrez Gene ID: | 29942 |
Gene Name: | purine rich element binding protein G |
Gene Aliases: |
PURG-A, PURG-B |
Location: |
Chr.8:30995802-31033715 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PURG | NM_001015508.2 | 1 | 129 | NP_001015508.1 |
| AF195513.2 | 1 | 129 | AAF03900.1 | |
| AY077841.1 | 1 | 129 | AAL77218.1 |
Target Gene Details
Entrez Gene ID: | 7486 |
Gene Name: | Werner syndrome RecQ like helicase |
Gene Aliases: |
RECQ3, RECQL2, RECQL3 |
Location: |
Chr.8:31033262-31173761 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WRN | NM_000553.4 | 1 | 326 | NP_000544.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1133688 | Chr.8:31032784 - 31033884 on Build GRCh38 | Deletion |
 WRN
PURG
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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