Genomic Map
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Target Gene Details
Entrez Gene ID: | 79728 |
Gene Name: | partner and localizer of BRCA2 |
Gene Aliases: |
FANCN, PNCA3 |
Location: |
Chr.16:23603162-23641357 on Build GRCh38 |
Assay Gene Location: | Within Exon 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PALB2 | NM_024675.3 | 13 | 3924 | NP_078951.2 |
| XM_011545946.2 | 13 | 4729 | XP_011544248.1 | |
| XM_011545947.2 | 12 | 4545 | XP_011544249.1 | |
| XM_011545948.2 | 14 | 4016 | XP_011544250.1 | |
| XM_017023671.1 | 11 | 4457 | XP_016879160.1 | |
| XM_017023672.1 | 11 | 3687 | XP_016879161.1 | |
| XM_017023673.1 | 12 | 3775 | XP_016879162.1 | |
| AK025469.1 | 10 | 2301 | BAB15140.1 | |
| AK299152.1 | 13 | 3821 | ||
| AL834425.1 | 10 | 3207 | CAD39086.1 | |
| BC044254.2 | 13 | 3851 | AAH44254.1 | |
| BE670820.1 | 1 | 146 | ||
| BX647125.1 | 13 | 3835 | ||
| BX647130.1 | 13 | 3877 | ||
| CR749637.1 | 13 | 3875 | CAH18431.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv819281 | Chr.16:23603209 - 23611345 on Build GRCh38 | Loss |
 PALB2
|
| esv3638230 | Chr.16:23596807 - 23605086 on Build GRCh38 | Gain |
PALB2
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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