Genomic Map
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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 Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WRN | NM_000553.4 | NP_000544.2 | ||
| XM_011544639.2 | XP_011542941.1 | |||
| AF091214.1 | AAC63361.1 | |||
| AY818673.1 | ||||
| BP279291.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv831278 | Chr.8:31059468 - 31213390 on Build GRCh38 | Gain |
 WRN
|
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Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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