Assay Details
Target Gene Details
Entrez Gene ID: | 79707 |
Gene Name: | nucleolar protein 9 |
Gene Aliases: |
Grc3, NET6 |
Location: |
Chr.1:6521347-6554598 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NOL9 | NM_024654.4 | 12 | 6568 | NP_078930.3 |
| AK026976.1 | 9 | 2415 | BAB15611.1 | |
| CA432392.1 | 1 | 161 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv7880 | Chr.1:6417968 - 6611914 on Build GRCh38 | Gain+Loss |
|
| nsv545268 | Chr.1:6490316 - 6578004 on Build GRCh38 | Loss |
|
| nsv831536 | Chr.1:6429326 - 6605343 on Build GRCh38 | Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs149443960] 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