Assay Details
Target Gene Details
Entrez Gene ID: | 10297 |
Gene Name: | APC2, WNT signaling pathway regulator |
Gene Aliases: |
APCL |
Location: |
Chr.19:1446268-1473244 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 5 - Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
APC2 | NM_005883.2 | NP_005874.1 | ||
XM_005259475.2 | XP_005259532.1 | |||
XM_006722607.2 | XP_006722670.1 | |||
XM_006722608.3 | XP_006722671.2 | |||
XM_006722609.3 | XP_006722672.1 | |||
XM_006722610.3 | XP_006722673.2 | |||
AB012162.1 | BAA34611.1 | |||
AF110334.1 | AAD28183.1 | |||
AF128222.1 | AAF01784.1 | |||
AJ012652.1 | CAB61207.1 | |||
AL078616.1 | ||||
BC032573.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv32942 | Chr.19:1320268 - 1999205 on Build GRCh38 | Gain+Loss |
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nsv578279 | Chr.19:1413575 - 1530061 on Build GRCh38 | Gain |
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nsv833705 | Chr.19:1380125 - 1544934 on Build GRCh38 | Loss |
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esv2758743 | Chr.19:951641 - 1544934 on Build GRCh38 | Gain+Loss |
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nsv953942 | Chr.19:1371602 - 2057401 on Build GRCh38 | Deletion |
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nsv470105 | Chr.19:1444420 - 1526614 on Build GRCh38 | Gain |
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![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)
More Information
Set Membership: |
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Gene Ontology Categories:
![](/order/genome-database/details/genotyping/assets/img/arrow_icon_up_black.png)