Assay Details
Target Gene Details
Entrez Gene ID: | 6018 |
Gene Name: | rearranged L-myc fusion |
Gene Aliases: |
ZN-15L, ZNF292L |
Location: |
Chr.1:40161369-40240921 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RLF | NM_012421.3 | NP_036553.2 | ||
| XM_017002016.1 | XP_016857505.1 | |||
| XM_017002017.1 | XP_016857506.1 | |||
| XM_017002018.1 | XP_016857507.1 | |||
| AK307662.1 | ||||
| BC113666.1 | ||||
| U22377.1 | AAC50396.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2758933 | Chr.1:39759471 - 40194760 on Build GRCh38 | Loss |
|
| nsv829660 | Chr.1:40073032 - 40266408 on Build GRCh38 | Gain+Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs145789441] 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