Assay Details
Target Gene Details
Entrez Gene ID: | 9792 |
Gene Name: | SERTA domain containing 2 |
Gene Aliases: |
Sei-2, TRIP-Br2 |
Location: |
Chr.2:64631621-64751091 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SERTAD2 | NM_014755.2 | 2 | 5385 | NP_055570.1 |
XM_005264669.2 | 2 | 5903 | XP_005264726.1 | |
XM_011533204.1 | 2 | 5122 | XP_011531506.1 | |
XM_011533205.2 | 2 | 5439 | XP_011531507.1 | |
BQ017415.1 | 1 | 181 | ||
D50917.1 | 2 | 5385 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv582127 | Chr.2:63618350 - 64923736 on Build GRCh38 | Gain | LOC647115 LINC00309 MIR4433A VPS54 MIR4434 WDPCP LOC400958 PELI1 LGALSL AFTPH MIR4433B LOC105374768 LOC339807 SERTAD2 LOC101927402 UGP2 LOC100507006 LOC101927438 |
nsv2756 | Chr.2:64588629 - 64633531 on Build GRCh38 | Deletion | AFTPH LOC339807 SERTAD2 |
More Information
Additional Information:
For this assay, SNP(s) [rs116991156] 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 |