Assay Details
Target Gene Details
Entrez Gene ID: | 203074 |
Gene Name: | protease, serine 55 |
Gene Aliases: |
CT153, T-SP1, TSP1, UNQ9391 |
Location: |
Chr.8:10525331-10554166 on Build GRCh38 |
Assay Gene Location: | Within Intron 8 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
PRSS55 | NM_001197020.1 | NP_001183949.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv610268 | Chr.8:10474126 - 10629142 on Build GRCh38 | Loss | PRSS55 LINCR-0001 RP1L1 |
nsv1025557 | Chr.8:10359216 - 10697677 on Build GRCh38 | Gain | MSRA PRSS55 MIR4286 LINCR-0001 C8orf74 RP1L1 |
nsv610267 | Chr.8:10411226 - 10669232 on Build GRCh38 | Gain | MSRA PRSS55 MIR4286 LINCR-0001 RP1L1 |
nsv1030934 | Chr.8:10207659 - 10703651 on Build GRCh38 | Gain | MSRA PRSS55 MIR4286 LINCR-0001 C8orf74 RP1L1 |
esv3572508 | Chr.8:10443405 - 10588192 on Build GRCh38 | Loss | PRSS55 LINCR-0001 |
More Information
Additional Information:
For this assay, SNP(s) [rs144735207] 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 |