Assay Details
Target Gene Details
Entrez Gene ID: | 5934 |
Gene Name: | RB transcriptional corepressor like 2 |
Gene Aliases: |
P130, Rb2 |
Location: |
Chr.16:53434420-53491648 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RBL2 | NM_001323608.1 | NP_001310537.1 | ||
| NM_001323609.1 | NP_001310538.1 | |||
| NM_001323610.1 | NP_001310539.1 | |||
| NM_001323611.1 | NP_001310540.1 | |||
| NM_005611.3 | NP_005602.3 | |||
| AK300047.1 | ||||
| AK307881.1 | ||||
| BC034490.1 | AAH34490.1 | |||
| DB017942.1 | ||||
| S67171.1 | AAB29227.1 | |||
| X74594.1 | CAA52671.1 | |||
| X76061.1 | CAA53661.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3638649 | Chr.16:53427199 - 53440126 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs71390206] 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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Genomic Map