Assay Details
Target Gene Details
Entrez Gene ID: | 10212 |
Gene Name: | DEAD-box helicase 39A |
Gene Aliases: |
BAT1, BAT1L, DDX39, DDXL, URH49 |
Location: |
Chr.19:14408798-14419383 on Build GRCh38 |
Assay Gene Location: | Within Intron 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DDX39A | NM_005804.3 | NP_005795.2 | ||
NR_046366.2 | ||||
XM_006722606.3 | XP_006722669.1 | |||
XM_011527620.1 | XP_011525922.1 | |||
AK293911.1 | ||||
AK301847.1 | ||||
BC001009.2 | AAH01009.1 | |||
BC032128.2 | AAH32128.1 | |||
DA432925.1 | ||||
DB032777.1 | ||||
U90426.1 | AAB50231.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1160590 | Chr.19:14398750 - 14462842 on Build GRCh38 | Deletion | PKN1 DDX39A ADGRE5 |
nsv833764 | Chr.19:14381787 - 14504061 on Build GRCh38 | Loss | PKN1 DDX39A GIPC1 PTGER1 ADGRE5 SNRPGP15 |
More Information
Additional Information:
For this assay, SNP(s) [rs147752807] 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 |