Assay Details
Target Gene Details
Entrez Gene ID: | 9529 |
Gene Name: | BCL2 associated athanogene 5 |
Gene Aliases: |
BAG-5 |
Location: |
Chr.14:103556544-103562814 on Build GRCh38 |
Assay Gene Location: | Within Exon 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| BAG5 | NM_001015048.2 | 2 | 3286 | NP_001015048.1 |
| NM_001015049.2 | 2 | 3493 | NP_001015049.1 | |
| NM_004873.3 | 2 | 3306 | NP_004864.1 | |
| AB020680.1 | 2 | 3116 | ||
| AB105186.1 | 2 | 3282 | ||
| AF095195.2 | 2 | 3282 | AAD16124.2 | |
| AK001378.1 | 1 | 2344 | ||
| AK023145.1 | 1 | 2813 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3635599 | Chr.14:103524781 - 103606409 on Build GRCh38 | Gain |
|
| nsv832883 | Chr.14:103461350 - 103654616 on Build GRCh38 | Loss |
|
| nsv566022 | Chr.14:103541218 - 103626452 on Build GRCh38 | Loss |
|
| nsv1054574 | Chr.14:103210111 - 105365114 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73361317] 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: |
|

Genomic Map