Genomic Map
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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 Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RBL2 | NM_001323608.1 | 3 | 577 | NP_001310537.1 |
| NM_001323609.1 | 3 | 577 | NP_001310538.1 | |
| NM_001323610.1 | 3 | 577 | NP_001310539.1 | |
| NM_001323611.1 | 3 | 326 | NP_001310540.1 | |
| NM_005611.3 | 3 | 558 | NP_005602.3 | |
| AK300047.1 | 3 | 296 | ||
| AK307881.1 | 3 | 535 | ||
| BC034490.1 | 3 | 548 | AAH34490.1 | |
| DB017942.1 | ||||
| S67171.1 | 3 | 468 | AAB29227.1 | |
| X74594.1 | 3 | 269 | CAA52671.1 | |
| X76061.1 | 3 | 509 | CAA53661.1 |
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Additional Information:
For this assay, SNP(s) [rs147880565] 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: |
Intragenic
Exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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