Assay Details
Target Gene Details
Entrez Gene ID: | 8886 |
Gene Name: | DEAD-box helicase 18 |
Gene Aliases: |
MrDb |
Location: |
Chr.2:117814679-117832377 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 9 - Intron 9 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DDX18 | NM_006773.3 | NP_006764.3 | ||
AB209392.1 | BAD92629.1 | |||
AK001467.1 | BAA91709.1 | |||
AK091227.1 | BAC03616.1 | |||
BC001238.1 | AAH01238.1 | |||
BC003360.1 | AAH03360.1 | |||
BC024739.1 | AAH24739.1 | |||
CR457060.1 | CAG33341.1 | |||
X98743.1 | CAA67295.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv999434 | Chr.2:117074067 - 117975257 on Build GRCh38 | Gain |
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nsv2889 | Chr.2:117811935 - 117840276 on Build GRCh38 | Insertion |
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More Information
Additional Information:
For this assay, SNP(s) [rs141313148] 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: |
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Gene Ontology Categories:
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