Assay Details
Target Gene Details
Entrez Gene ID: | 23279 |
Gene Name: | nucleoporin 160 |
Gene Aliases: |
- |
Location: |
Chr.11:47778083-47848544 on Build GRCh38 |
Assay Gene Location: | Within Exon 35 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NUP160 | NM_015231.2 | 36 | 4428 | NP_056046.1 |
| NR_134636.1 | 36 | 4443 | ||
| AK304308.1 | 36 | 4214 | ||
| AL832029.1 | 36 | 4216 | ||
| AL832813.1 | 5 | 530 | ||
| BC008700.1 | 7 | 711 | AAH08700.1 | |
| BC125227.1 | 36 | 4351 | ||
| BC125228.1 | 36 | 4351 | ||
| BX647634.1 | 36 | 4228 | ||
| D83781.1 | BAA12110.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv469858 | Chr.11:47625963 - 47815620 on Build GRCh38 | Gain |
|
| dgv1111n100 | Chr.11:47653918 - 48644472 on Build GRCh38 | Gain |
|
| nsv832143 | Chr.11:47679256 - 47861988 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs56962998] 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