Genomic Map
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Target Gene Details
Entrez Gene ID: | 7484 |
Gene Name: | Wnt family member 9B |
Gene Aliases: |
WNT14B, WNT15 |
Location: |
Chr.17:46833201-46886730 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WNT9B | XM_011525178.2 | XP_011523480.1 | ||
| AK127268.1 | BAC86908.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1070832 | Chr.17:46794133 - 46836434 on Build GRCh38 | Deletion |
 WNT3
WNT9B
|
| esv2656635 | Chr.17:46204086 - 47091135 on Build GRCh38 | Deletion |
WNT3
KANSL1
LRRC37A
WNT9B
LOC107987253
LOC107987254
NSF
NSFP1
RPRML
MIR5089
ARL17B
ARL17A
GOSR2
LRRC37A2
|
| dgv1475n106 | Chr.17:46794234 - 46836534 on Build GRCh38 | Deletion |
WNT3
WNT9B
|
| esv2758692 | Chr.17:46006548 - 47199967 on Build GRCh38 | Gain+Loss |
WNT3
KANSL1
LRRC37A
RPS2P47
WNT9B
LOC107987253
MAPT
LOC107987254
NSF
CDC27
NSFP1
RPRML
MIR5089
ARL17B
KANSL1-AS1
ARL17A
GOSR2
LRRC37A2
|
| nsv428343 | Chr.17:46314456 - 46836265 on Build GRCh38 | Gain+Loss |
NSFP1
WNT3
LRRC37A
WNT9B
LOC107987253
ARL17B
LOC107987254
ARL17A
NSF
LRRC37A2
|
Back To TopMore Information
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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