Assay Details
Target Gene Details
Entrez Gene ID: | 8839 |
Gene Name: | WNT1 inducible signaling pathway protein 2 |
Gene Aliases: |
CCN5, CT58, CTGF-L |
Location: |
Chr.20:44714204-44728041 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 4 - Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WISP2 | NM_001323369.1 | NP_001310298.1 | ||
| NM_001323370.1 | NP_001310299.1 | |||
| NM_003881.3 | NP_003872.1 | |||
| XM_017028116.1 | XP_016883605.1 | |||
| AF074604.1 | AAC26794.1 | |||
| AF083500.1 | AAC70350.1 | |||
| AF100780.1 | AAC96322.1 | |||
| AK129660.1 | BAC85210.1 | |||
| AK313853.1 | ||||
| AY358915.1 | AAQ89274.1 | |||
| BC017782.2 | AAH17782.1 | |||
| BC058074.1 | AAH58074.1 | |||
| BC064379.1 | AAH64379.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv458985 | Chr.20:44706933 - 44779789 on Build GRCh38 | Gain |
|
| nsv179790 | Chr.20:44721538 - 44731454 on Build GRCh38 | Deletion |
|
| nsv1056102 | Chr.20:44673341 - 45636248 on Build GRCh38 | Loss |
|
More Information
Set Membership: |
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Genomic Map