Assay Details
Target Gene Details
Entrez Gene ID: | 91646 |
Gene Name: | tudor domain containing 12 |
Gene Aliases: |
ECAT8 |
Location: |
Chr.19:32719773-32829580 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TDRD12 | NM_001110822.1 | NP_001104292.1 | ||
| XM_011527471.2 | XP_011525773.1 | |||
| XM_011527472.2 | XP_011525774.1 | |||
| XM_011527473.2 | XP_011525775.1 | |||
| XM_011527474.2 | XP_011525776.1 | |||
| XM_011527475.2 | XP_011525777.1 | |||
| XM_011527476.2 | XP_011525778.1 | |||
| XM_017027458.1 | XP_016882947.1 | |||
| BI769394.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1067189 | Chr.19:32712741 - 32816579 on Build GRCh38 | Loss |
|
| nsv511617 | Chr.19:32719341 - 32730420 on Build GRCh38 | Loss |
|
| esv2670459 | Chr.19:32717931 - 32733018 on Build GRCh38 | Deletion |
|
| nsv953276 | Chr.19:32719895 - 32721094 on Build GRCh38 | Deletion |
|
| esv3644177 | Chr.19:32717978 - 32732982 on Build GRCh38 | Loss |
|
| nsv458535 | Chr.19:32716739 - 32824007 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs115656400] 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