Genomic Map
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Target Gene Details
Entrez Gene ID: | 54879 |
Gene Name: | suppression of tumorigenicity 7 like |
Gene Aliases: |
FAM4B, ST7R, STLR |
Location: |
Chr.1:112517444-112620838 on Build GRCh38 |
Assay Gene Location: | Within Intron 22 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ST7L | XM_011541628.2 | XP_011539930.1 |
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 Exon 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| WNT2B | NM_001291880.1 | 5 | 2470 | NP_001278809.1 |
| NM_004185.4 | 6 | 2541 | NP_004176.2 | |
| NM_024494.2 | 5 | 2116 | NP_078613.1 | |
| AK127449.1 | 5 | 2470 | ||
| AK307185.1 | 2 | 809 | ||
| BC141825.1 | 5 | 2116 |
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 |
 MIR4256
ST7L
WNT2B
CTTNBP2NL
|
| esv27061 | Chr.1:112150007 - 112703641 on Build GRCh38 | Gain+Loss |
MIR4256
ST7L
MOV10
WNT2B
CTTNBP2NL
RHOC
CAPZA1
|
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Additional Information:
Set Membership: |
Intragenic
Exonic
Intronic
Non-exonic
DGV Variation
Validated
|
Panther Classification:
Gene Ontology Categories:
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