Assay Details
Target Gene Details
Entrez Gene ID: | 51449 |
Gene Name: | prenylcysteine oxidase 1 |
Gene Aliases: |
PCL1 |
Location: |
Chr.2:70258099-70281185 on Build GRCh38 |
Assay Gene Location: | Within Exon 6 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PCYOX1 | NM_016297.3 | 6 | 2224 | NP_057381.3 |
AB020715.1 | 6 | 2162 | ||
BC007029.1 | 4 | 1803 | AAH07029.1 | |
BC051891.1 | 6 | 2211 | AAH51891.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv518294 | Chr.2:70111212 - 70301469 on Build GRCh38 | Loss | LOC100133985 FAM136A MIR1285-2 SNRPG C2orf42 TIA1 PCYOX1 |
esv2760537 | Chr.2:70270692 - 70413622 on Build GRCh38 | Gain | FAM136A SNRPG PCYOX1 |
More Information
Additional Information:
For this assay, SNP(s) [rs76039898] 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 |