Assay Details
Target Gene Details
Entrez Gene ID: | 285855 |
Gene Name: | ribosomal protein L7 like 1 |
Gene Aliases: |
dJ475N16.4 |
Location: |
Chr.6:42879163-42889896 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RPL7L1 | NM_198486.3 | NP_940888.3 | ||
| NR_134562.1 | ||||
| NR_134563.1 | ||||
| XM_017010780.1 | XP_016866269.1 | |||
| AK021904.1 | ||||
| AK091341.1 | ||||
| AK291310.1 | ||||
| AK291949.1 | ||||
| AK297324.1 | ||||
| AK299816.1 | ||||
| BC058020.1 | AAH58020.1 | |||
| BC073890.1 | AAH73890.1 | |||
| HY089482.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv830651 | Chr.6:42845563 - 43000871 on Build GRCh38 | Loss |
|
| esv3576145 | Chr.6:42728097 - 43012090 on Build GRCh38 | Gain |
|
| nsv1017398 | Chr.6:42659705 - 43400998 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs72864272] 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