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: | Overlaps - Exon 3 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
BAG5 | NM_001015048.2 | NP_001015048.1 | ||
NM_001015049.2 | NP_001015049.1 | |||
NM_004873.3 | NP_004864.1 | |||
AB105186.1 | ||||
CA424706.1 |
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 |
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nsv832883 | Chr.14:103461350 - 103654616 on Build GRCh38 | Loss |
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nsv566022 | Chr.14:103541218 - 103626452 on Build GRCh38 | Loss |
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nsv1054574 | Chr.14:103210111 - 105365114 on Build GRCh38 | Loss |
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More Information
Additional Information:
For this assay, SNP(s) [rs76005268] 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: |
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Gene Ontology Categories:
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