Assay Details
Target Gene Details
Entrez Gene ID: | 28954 |
Gene Name: | RRAD and GEM like GTPase 1 |
Gene Aliases: |
GD:REM, GES |
Location: |
Chr.20:31475273-31484905 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| REM1 | NM_014012.5 | 5 | 1537 | NP_054731.2 |
| XM_005260404.1 | 5 | 1561 | XP_005260461.1 | |
| XM_011528795.1 | 5 | 1555 | XP_011527097.1 | |
| XM_017027833.1 | 5 | 1395 | XP_016883322.1 | |
| AF152863.1 | 5 | 1519 | AAF74212.1 | |
| BC039813.1 | 5 | 1523 | AAH39813.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv470546 | Chr.20:31245806 - 31647499 on Build GRCh38 | Gain |
|
| esv2763228 | Chr.20:31247246 - 31651719 on Build GRCh38 | Gain |
|
| dgv4300n100 | Chr.20:31247234 - 32033468 on Build GRCh38 | Gain |
|
| nsv458961 | Chr.20:31305698 - 31688103 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs73620401] 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