Genomic Map
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Target Gene Details
Entrez Gene ID: | 7482 |
Gene Name: | Wnt family member 2B |
Gene Aliases: |
WNT13 |
Location: |
Chr.1:112466541-112521288 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WNT2B | NM_001291880.1 | NP_001278809.1 | ||
| NM_004185.4 | NP_004176.2 | |||
| NM_024494.2 | NP_078613.1 | |||
| AB045116.1 | BAB11984.1 | |||
| AB045117.1 | BAB11985.1 | |||
| AK127449.1 | ||||
| AK312696.1 | ||||
| BC141825.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv831081 | Chr.1:112392298 - 112580018 on Build GRCh38 | Loss |
 CTTNBP2NL
ST7L
WNT2B
MIR4256
|
| esv1009068 | Chr.1:112506370 - 112514785 on Build GRCh38 | Deletion |
WNT2B
|
| esv27061 | Chr.1:112150007 - 112703641 on Build GRCh38 | Gain+Loss |
CTTNBP2NL
ST7L
WNT2B
CAPZA1
RHOC
MOV10
MIR4256
|
| nsv951397 | Chr.1:112503479 - 112511378 on Build GRCh38 | Deletion |
WNT2B
|
| nsv1008375 | Chr.1:112485649 - 112517599 on Build GRCh38 | Loss |
ST7L
WNT2B
|
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Additional Information:
For this assay, SNP(s) [rs113535807] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Intronic
Non-exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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