Assay Details
Target Gene Details
Entrez Gene ID: | 5651 |
Gene Name: | transmembrane protease, serine 15 |
Gene Aliases: |
ENTK, PRSS7 |
Location: |
Chr.21:18269107-18403806 on Build GRCh38 |
Assay Gene Location: | Within Intron 26 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
TMPRSS15 | NM_002772.2 | NP_002763.2 | ||
XM_011529654.1 | XP_011527956.1 | |||
XM_011529655.1 | XP_011527957.1 | |||
XM_011529656.2 | XP_011527958.1 | |||
XM_011529657.1 | XP_011527959.1 | |||
XM_011529658.1 | XP_011527960.1 | |||
XM_011529659.1 | XP_011527961.1 | |||
BC111749.1 | AAI11750.1 | |||
KF688184.1 | ||||
U09860.1 | AAC50138.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
esv2751925 | Chr.21:18035494 - 21000411 on Build GRCh38 | Loss | MIR548XHG MIR548X NCAM2 CHODL LINC00320 TMPRSS15 |
nsv587137 | Chr.21:18237846 - 18282481 on Build GRCh38 | Loss | CHODL TMPRSS15 |
More Information
Additional Information:
For this assay, SNP(s) [rs73320107] 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 |