Assay Details
Target Gene Details
Entrez Gene ID: | 78991 |
Gene Name: | prenylcysteine oxidase 1 like |
Gene Aliases: |
- |
Location: |
Chr.5:149358007-149375112 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PCYOX1L | NM_001301054.1 | NP_001287983.1 | ||
NM_001301057.1 | NP_001287986.1 | |||
NM_024028.3 | NP_076933.3 | |||
XM_011537680.1 | XP_011535982.1 | |||
AF451985.1 | AAP97684.1 | |||
AK075414.1 | BAC11604.1 | |||
BC000014.2 | AAH00014.1 | |||
DA368718.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv599948 | Chr.5:149346599 - 149413198 on Build GRCh38 | Loss | IL17B GRPEL2-AS1 CARMN GRPEL2 PCYOX1L |
More Information
Additional Information:
For this assay, SNP(s) [rs114596774] 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 Intronic Non-exonic DGV Variation |