Assay Details
Target Gene Details
Entrez Gene ID: | 51657 |
Gene Name: | serine/threonine/tyrosine interacting-like 1 |
Gene Aliases: |
DUSP24, MK-STYX, MKSTYX |
Location: |
Chr.7:75995820-76048709 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv821252 | Chr.7:76033649 - 76039546 on Build GRCh38 | Deletion | STYXL1 |
nsv428173 | Chr.7:75934531 - 76173362 on Build GRCh38 | Gain | LOC107986711 STYXL1 GTF2IP7 SNORA14A POR MDH2 TMEM120A |
nsv528969 | Chr.7:75074053 - 76920728 on Build GRCh38 | Gain | CCL26 GTF2IP7 SNORA14A CCL24 MDH2 SSC4D TMEM120A PMS2P2 HIP1 LOC100133091 LOC105375355 PMS2P3 YWHAG MIR4651 LOC541473 LOC107986711 NCF1C NSUN5P1 SPDYE16 SRRM3 POR HSPB1 ZP3 LOC441259 DTX2 TRIM73 STAG3L1 STYXL1 SPDYE5 PMS2P10 FDPSP2 RHBDD2 POM121C GTF2IRD2B GTF2IP1 POMZP3 |
esv3613750 | Chr.7:76031380 - 76045732 on Build GRCh38 | Loss | STYXL1 |
esv3613742 | Chr.7:75912784 - 76036530 on Build GRCh38 | Loss | STYXL1 SNORA14A POR MIR4651 TMEM120A |
esv3613749 | Chr.7:76009631 - 76035709 on Build GRCh38 | Loss | STYXL1 |
dgv120n16 | Chr.7:75440769 - 76641919 on Build GRCh38 | Deletion | CCL26 GTF2IP7 SNORA14A CCL24 MDH2 SSC4D TMEM120A HIP1 LOC100133091 LOC105375355 PMS2P3 YWHAG MIR4651 LOC107986711 SPDYE16 SRRM3 POR HSPB1 ZP3 DTX2 STYXL1 SPDYE5 FDPSP2 RHBDD2 POM121C POMZP3 |
More Information
Additional Information:
For this assay, SNP(s) [rs77381667] 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 |