Assay Details
Target Gene Details
Entrez Gene ID: | 391013 |
Gene Name: | phospholipase A2 group IIC |
Gene Aliases: |
- |
Location: |
Chr.1:20163085-20177364 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PLA2G2C | NM_001316722.1 | NP_001303651.1 | ||
| XM_017001270.1 | XP_016856759.1 | |||
| AW135717.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2674003 | Chr.1:20172236 - 20174073 on Build GRCh38 | Deletion |
|
| esv26309 | Chr.1:20172511 - 20174305 on Build GRCh38 | Loss |
|
| esv3585417 | Chr.1:20172265 - 20174165 on Build GRCh38 | Loss |
|
| nsv545731 | Chr.1:19989106 - 20776306 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs114411177] 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