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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 32 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
WRN | NM_000553.4 | 32 | 4521 | NP_000544.2 |
XM_011544639.2 | 31 | 3922 | XP_011542941.1 | |
XM_011544640.1 | 20 | 2234 | XP_011542942.1 | |
AB209652.1 | 18 | 1964 | BAD92889.1 | |
AF091214.1 | 32 | 3964 | AAC63361.1 | |
AL833572.1 | 20 | 2367 | ||
AY818673.1 | 31 | 3733 |
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1020927 | Chr.8:31140506 - 31162968 on Build GRCh38 | Loss | WRN |
nsv831278 | Chr.8:31059468 - 31213390 on Build GRCh38 | Gain | WRN |
Set Membership: |
Intragenic Exonic DGV Variation |