Assay Details
Target Gene Details
Entrez Gene ID: | 2802 |
Gene Name: | golgin A3 |
Gene Aliases: |
GCP170, MEA-2 |
Location: |
Chr.12:132768909-132829131 on Build GRCh38 |
Assay Gene Location: | Within Exon 27 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| GOLGA3 | NM_005895.3 | 24 | 5449 | NP_005886.2 |
| XM_005266164.4 | 24 | 5056 | XP_005266221.1 | |
| XM_005266167.4 | 21 | 4481 | XP_005266224.1 | |
| XM_006719736.3 | 24 | 5176 | XP_006719799.1 | |
| XM_006719737.3 | 24 | 5186 | XP_006719800.1 | |
| XM_011534793.2 | 23 | 4903 | XP_011533095.1 | |
| XM_011534794.2 | 16 | 3054 | XP_011533096.1 | |
| D63997.1 | 24 | 5154 | BAA23661.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3631312 | Chr.12:132735138 - 132794488 on Build GRCh38 | Loss |
|
| nsv455811 | Chr.12:132769585 - 132814368 on Build GRCh38 | Loss |
|
| esv3631316 | Chr.12:132771535 - 132796367 on Build GRCh38 | Loss |
|
| esv3580555 | Chr.12:132760405 - 132796737 on Build GRCh38 | Loss |
|
| nsv1037074 | Chr.12:132613063 - 132801953 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs115355148] 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