Assay Details
Target Gene Details
Entrez Gene ID: | 137902 |
Gene Name: | peroxidasin like |
Gene Aliases: |
PMR1, PRM1, VPO2 |
Location: |
Chr.8:51319575-51811031 on Build GRCh38 |
Assay Gene Location: | Within Intron 22 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PXDNL | NM_144651.4 | NP_653252.3 | ||
| XM_005251168.3 | XP_005251225.1 | |||
| XM_006716420.3 | XP_006716483.1 | |||
| XM_011517456.2 | XP_011515758.1 | |||
| XM_011517457.2 | XP_011515759.1 | |||
| XM_011517458.2 | XP_011515760.1 | |||
| XM_017013041.1 | XP_016868530.1 | |||
| AK058200.1 | BAB71713.1 | |||
| AK131524.1 | BAD18663.1 | |||
| AY877349.1 | ||||
| EU170240.1 | ||||
| KJ545488.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv817615 | Chr.8:51339845 - 52110824 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs116259444,rs75077202] 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