Assay Details
Target Gene Details
Entrez Gene ID: | 151835 |
Gene Name: | copine family member 9 |
Gene Aliases: |
- |
Location: |
Chr.3:9703807-9729908 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 14 - Intron 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CPNE9 | NM_001308388.1 | NP_001295317.1 | ||
| NM_153635.2 | NP_705899.2 | |||
| XM_011533386.2 | XP_011531688.1 | |||
| XM_011533388.2 | XP_011531690.1 | |||
| XM_011533389.2 | XP_011531691.1 | |||
| XM_017005747.1 | XP_016861236.1 | |||
| BC035735.1 | ||||
| BC130375.1 | ||||
| BU101942.1 | ||||
| BX453546.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1010768 | Chr.3:9502870 - 9873902 on Build GRCh38 | Gain |
|
| nsv1008805 | Chr.3:9694224 - 9756456 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs76573035] 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