Assay Details
Target Gene Details
Entrez Gene ID: | 84910 |
Gene Name: | transmembrane protein 87B |
Gene Aliases: |
- |
Location: |
Chr.2:112055223-112119318 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| TMEM87B | NM_032824.2 | NP_116213.1 | ||
| XM_005263827.2 | XP_005263884.1 | |||
| XM_006712807.2 | XP_006712870.1 | |||
| XM_017005121.1 | XP_016860610.1 | |||
| AK027587.1 | BAB55214.1 | |||
| AK074243.1 | ||||
| AK290294.1 | ||||
| BC115373.1 | AAI15374.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3893093 | Chr.2:111912373 - 112100908 on Build GRCh38 | Gain |
|
| nsv582699 | Chr.2:110763166 - 112172487 on Build GRCh38 | Loss |
|
| nsv521956 | Chr.2:110634682 - 112341235 on Build GRCh38 | Loss |
|
| dgv4047n100 | Chr.2:110308696 - 112358403 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs72942003] 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