Assay Details
Target Gene Details
Entrez Gene ID: | 119587 |
Gene Name: | carboxypeptidase X (M14 family), member 2 |
Gene Aliases: |
CPX2, UNQ676 |
Location: |
Chr.10:123745636-123944094 on Build GRCh38 |
Assay Gene Location: | Overlaps - Exon 21 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| CPXM2 | NM_198148.2 | NP_937791.2 | ||
| XM_011539285.2 | XP_011537587.1 | |||
| XM_011539286.1 | XP_011537588.1 | |||
| XM_017015673.1 | XP_016871162.1 | |||
| XM_017015674.1 | XP_016871163.1 | |||
| AL833732.1 | CAH56260.1 | |||
| AY358565.1 | AAQ88928.1 | |||
| BC027623.1 | AAH27623.1 | |||
| BC036789.1 | AAH36789.2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv25320 | Chr.10:123744994 - 123745657 on Build GRCh38 | Deletion |
|
| nsv832011 | Chr.10:123590498 - 123760281 on Build GRCh38 | Gain+Loss |
|
More Information
Additional Information:
For this assay, SNP(s) [rs113621618] 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: |
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Genomic Map