Genomic Map
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Target Gene Details
Entrez Gene ID: | 10241 |
Gene Name: | calcium binding and coiled-coil domain 2 |
Gene Aliases: |
NDP52 |
Location: |
Chr.17:48830988-48865245 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 1 - Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CALCOCO2 | NM_001261390.1 | NP_001248319.1 | ||
| NM_001261391.1 | NP_001248320.1 | |||
| NM_001261393.1 | NP_001248322.1 | |||
| NM_001261395.1 | NP_001248324.1 | |||
| NM_005831.4 | NP_005822.1 | |||
| AK222666.1 | BAD96386.1 | |||
| AK223227.1 | BAD96947.1 | |||
| AK293137.1 | ||||
| AK293329.1 | ||||
| AK298177.1 | ||||
| AK303313.1 | ||||
| AK304024.1 | ||||
| AK310648.1 | ||||
| AK314796.1 | ||||
| AL042638.1 | ||||
| AL046722.1 | ||||
| BC004130.2 | AAH04130.1 | |||
| BG773301.1 | ||||
| U22897.1 | AAA75297.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv29639 | Chr.17:48827524 - 48831068 on Build GRCh38 | Loss |
 CALCOCO2
|
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Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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