Assay Details
Target Gene Details
Entrez Gene ID: | 90019 |
Gene Name: | synaptotagmin 8 |
Gene Aliases: |
- |
Location: |
Chr.11:1827484-1837521 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SYT8 | XM_011520455.1 | XP_011518757.1 | ||
| XM_011520456.2 | XP_011518758.1 | |||
| XM_011520457.2 | XP_011518759.1 | |||
| XM_017018528.1 | XP_016874017.1 | |||
| XM_017018529.1 | XP_016874018.1 | |||
| AK131292.1 | BAD18463.1 | |||
| AK293395.1 | ||||
| AL137708.1 | 1 | 297 | CAB70885.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1047474 | Chr.11:1803515 - 2043381 on Build GRCh38 | Gain |
|
| nsv553050 | Chr.11:1813024 - 1884944 on Build GRCh38 | Loss |
|
| nsv951281 | Chr.11:1821171 - 1858170 on Build GRCh38 | Deletion |
|
| esv29980 | Chr.11:1820597 - 2097889 on Build GRCh38 | Loss |
|
| nsv553047 | Chr.11:1733170 - 2418537 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs115318351] 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