Assay Details
Target Gene Details
Entrez Gene ID: | 352954 |
Gene Name: | GATS, stromal antigen 3 opposite strand |
Gene Aliases: |
STAG3OS |
Location: |
Chr.7:100187988-100272274 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| GATS | NM_178831.6 | NP_849153.3 | ||
| NR_028038.1 | 7 | 1555 | ||
| NR_028039.1 | 7 | 1555 | ||
| NR_028040.1 | ||||
| XM_017012153.1 | 5 | 2398 | XP_016867642.1 | |
| XM_017012154.1 | XP_016867643.1 | |||
| XM_017012155.1 | XP_016867644.1 | |||
| XM_017012156.1 | XP_016867645.1 | |||
| XM_017012157.1 | XP_016867646.1 | |||
| AK056608.1 | ||||
| AK091418.1 | 5 | 720 | ||
| AK092358.1 | 7 | 1313 | BAC03870.1 | |
| AK095056.1 | ||||
| AK124689.1 | 1 | 1806 | ||
| AK290510.1 | ||||
| AL831967.2 | 1 | 1930 | ||
| BC033723.1 | AAH33723.1 | |||
| BC065200.1 | AAH65200.1 | |||
| BC090867.1 | 7 | 1530 | AAH90867.1 | |
| CR749506.1 | CAH18327.1 | |||
| DA737015.1 |
Target Gene Details
Entrez Gene ID: | 10734 |
Gene Name: | stromal antigen 3 |
Gene Aliases: |
- |
Location: |
Chr.7:100177563-100219334 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 30 - Exon 31 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| STAG3 | NM_001282716.1 | NP_001269645.1 | ||
| NM_001282717.1 | NP_001269646.1 | |||
| NM_001282718.1 | NP_001269647.1 | |||
| NM_012447.3 | NP_036579.2 | |||
| XM_011515742.1 | XP_011514044.1 | |||
| XM_017011683.1 | XP_016867172.1 | |||
| XM_017011684.1 | XP_016867173.1 | |||
| XM_017011685.1 | XP_016867174.1 | |||
| XM_017011686.1 | XP_016867175.1 | |||
| XM_017011687.1 | XP_016867176.1 | |||
| AJ007798.2 | CAB59367.1 | |||
| AK292394.1 | ||||
| AK302587.1 | ||||
| AK302693.1 | ||||
| AL833816.1 | CAD38679.2 | |||
| BC140932.1 | ||||
| BC146806.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2734888 | Chr.7:99975623 - 101290285 on Build GRCh38 | Deletion |
|
| nsv428180 | Chr.7:100153358 - 100363277 on Build GRCh38 | Gain |
|
| nsv8182 | Chr.7:100202193 - 100282158 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs80044214] 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