Assay Details
Target Gene Details
Entrez Gene ID: | 29118 |
Gene Name: | DEAD-box helicase 25 |
Gene Aliases: |
GRTH |
Location: |
Chr.11:125903275-125923110 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DDX25 | XM_017017626.1 | XP_016873115.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv248n67 | Chr.11:125843561 - 125919531 on Build GRCh38 | Gain | PUS3 LOC105369553 DDX25 HYLS1 |
nsv556525 | Chr.11:125690285 - 125971104 on Build GRCh38 | Gain | PUS3 LOC105369553 PATE3 PATE2 DDX25 LOC338667 PATE1 PATE4 HYLS1 CDON |
esv32964 | Chr.11:125495069 - 126046387 on Build GRCh38 | Gain+Loss | LOC403312 PUS3 FEZ1 PATE3 PATE2 ACRV1 PATE4 LOC105369553 DDX25 LOC338667 PATE1 STT3A-AS1 STT3A CHEK1 HYLS1 EI24 CDON |
More Information
Additional Information:
For this assay, SNP(s) [rs149329218] 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 |