Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 10521 |
Gene Name: | DEAD-box helicase 17 |
Gene Aliases: |
P72, RH70 |
Location: |
Chr.22:38483438-38506340 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DDX17 | NM_001098504.1 | 13 | 4599 | NP_001091974.1 |
| NM_006386.4 | 13 | 4593 | NP_006377.2 | |
| AB209595.1 | 14 | 4521 | BAD92832.1 | |
| AL080113.1 | 1 | 1470 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv834195 | Chr.22:38300366 - 38490431 on Build GRCh38 | Loss |
 LOC400927
LOC101927183
DDX17
LOC400927-CSNK1E
KDELR3
KCNJ4
CSNK1E
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs148319213] 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
|
Gene Ontology Categories:
Back To Top