Genomic Map
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Target Gene Details
Entrez Gene ID: | 7473 |
Gene Name: | Wnt family member 3 |
Gene Aliases: |
INT4, TETAMS |
Location: |
Chr.17:46762506-46818760 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WNT3 | NM_030753.4 | NP_110380.1 | ||
| AB067628.1 | BAB70502.1 | |||
| AY009397.1 | AAG38657.1 | |||
| BC112116.1 | AAI12117.1 | |||
| BC112118.1 | AAI12119.1 | |||
| BC114219.1 | AAI14220.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv5673n54 | Chr.17:46771330 - 46772268 on Build GRCh38 | Loss |
 WNT3
|
| dgv5671n54 | Chr.17:46771279 - 46772165 on Build GRCh38 | Gain+Loss |
WNT3
|
| nsv575460 | Chr.17:46771550 - 46772216 on Build GRCh38 | Gain+Loss |
WNT3
|
| nsv833465 | Chr.17:46629130 - 46812383 on Build GRCh38 | Loss |
WNT3
NSF
|
| esv28523 | Chr.17:46771088 - 46772335 on Build GRCh38 | Loss |
WNT3
|
| esv2656635 | Chr.17:46204086 - 47091135 on Build GRCh38 | Deletion |
MIR5089
WNT3
WNT9B
LRRC37A
NSFP1
NSF
ARL17B
LOC107987253
LRRC37A2
KANSL1
RPRML
ARL17A
GOSR2
LOC107987254
|
| esv2758692 | Chr.17:46006548 - 47199967 on Build GRCh38 | Gain+Loss |
MIR5089
MAPT
WNT3
WNT9B
LRRC37A
RPS2P47
CDC27
NSFP1
NSF
ARL17B
LOC107987253
LRRC37A2
KANSL1
RPRML
ARL17A
KANSL1-AS1
GOSR2
LOC107987254
|
| nsv428343 | Chr.17:46314456 - 46836265 on Build GRCh38 | Gain+Loss |
ARL17B
LOC107987253
LRRC37A2
WNT3
WNT9B
LRRC37A
ARL17A
LOC107987254
NSFP1
NSF
|
| dgv5670n54 | Chr.17:46771072 - 46772268 on Build GRCh38 | Gain |
WNT3
|
| nsv483083 | Chr.17:46654819 - 46812153 on Build GRCh38 | Gain |
WNT3
NSF
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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