Assay Details
Target Gene Details
Entrez Gene ID: | 647174 |
Gene Name: | serpin family E member 3 |
Gene Aliases: |
- |
Location: |
Chr.13:51334976-51362391 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SERPINE3 | NM_001101320.1 | NP_001094790.1 | ||
XM_017020707.1 | XP_016876196.1 | |||
AM402969.1 | ||||
AX772926.1 | CAE06272.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv832611 | Chr.13:51192336 - 51364178 on Build GRCh38 | Loss | INTS6 SERPINE3 FAM124A MIR5693 |
nsv561618 | Chr.13:49907577 - 51521449 on Build GRCh38 | Loss | MIR3613 LINC00371 DLEU2 DLEU7 DLEU1 TRIM13 GUCY1B2 INTS6-AS1 ST13P4 DLEU7-AS1 SPRYD7 MIR5693 RNASEH2B MIR16-1 KCNRG INTS6 RNASEH2B-AS1 MIR15A SERPINE3 FAM124A DLEU1-AS1 |
nsv1041 | Chr.13:51325852 - 51352515 on Build GRCh38 | Insertion | SERPINE3 MIR5693 |
More Information
Additional Information:
For this assay, SNP(s) [rs200479359] 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 |