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 Exon 24 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PXDNL | NM_144651.4 | 21 | 4211 | NP_653252.3 |
XM_005251168.3 | 7 | 2358 | XP_005251225.1 | |
XM_006716420.3 | 19 | 5509 | XP_006716483.1 | |
XM_011517456.2 | 20 | 5725 | XP_011515758.1 | |
XM_011517457.2 | 20 | 5725 | XP_011515759.1 | |
XM_011517458.2 | 19 | 3885 | XP_011515760.1 | |
XM_017013041.1 | 18 | 3846 | XP_016868530.1 | |
AK058200.1 | 5 | 1431 | BAB71713.1 | |
AK131524.1 | BAD18663.1 | |||
AY877349.1 | 21 | 4211 | ||
DB337228.1 | ||||
EU170240.1 | 21 | 4110 | ||
KJ545488.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv6190 | Chr.8:51338636 - 51367877 on Build GRCh38 | Insertion | PXDNL |
More Information
Additional Information:
For this assay, SNP(s) [rs138123996] 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: |
Intragenic Exonic DGV Variation |