Assay Details
Target Gene Details
Entrez Gene ID: | 6256 |
Gene Name: | retinoid X receptor alpha |
Gene Aliases: |
NR2B1 |
Location: |
Chr.9:134326463-134440586 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RXRA | NM_002957.5 | NP_002948.1 | ||
| AB307705.1 | ||||
| AK090416.1 | BAC03397.1 | |||
| BC063827.1 | AAH63827.1 | |||
| BC110998.1 | AAI10999.1 | |||
| BQ220698.1 | ||||
| HQ692843.1 | ||||
| X52773.1 | CAA36982.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| dgv7722n100 | Chr.9:134261330 - 134467038 on Build GRCh38 | Gain |
|
| dgv7723n100 | Chr.9:134309226 - 134469090 on Build GRCh38 | Gain |
|
| esv2739138 | Chr.9:132727483 - 135521553 on Build GRCh38 | Deletion |
|
| nsv466634 | Chr.9:134305392 - 134374858 on Build GRCh38 | Loss |
|
| nsv615804 | Chr.9:134290253 - 134351537 on Build GRCh38 | Loss |
|
| nsv831750 | Chr.9:134213606 - 134335327 on Build GRCh38 | Gain+Loss |
|
| nsv951809 | Chr.9:134324255 - 134506754 on Build GRCh38 | Deletion |
|
| nsv469908 | Chr.9:134278568 - 134445511 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73567668] 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