Assay Details
Target Gene Details
Entrez Gene ID: | 57696 |
Gene Name: | DEAD-box helicase 55 |
Gene Aliases: |
- |
Location: |
Chr.12:123602077-123620943 on Build GRCh38 |
Assay Gene Location: | Within Exon 12 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DDX55 | NM_020936.2 | 14 | 1817 | NP_065987.1 |
NR_135104.1 | 14 | 1889 | ||
NR_135105.1 | 14 | 1801 | ||
XM_017019710.1 | 14 | 1856 | XP_016875199.1 | |
XM_017019711.1 | 13 | 1911 | XP_016875200.1 | |
XM_017019712.1 | 14 | 1709 | XP_016875201.1 | |
XM_017019713.1 | 14 | 1832 | XP_016875202.1 | |
XM_017019714.1 | 15 | 1990 | XP_016875203.1 | |
XM_017019715.1 | 12 | 1557 | XP_016875204.1 | |
XM_017019716.1 | 12 | 1502 | XP_016875205.1 | |
XM_017019717.1 | 14 | 1754 | XP_016875206.1 | |
XM_017019718.1 | 12 | 2172 | XP_016875207.1 | |
XM_017019719.1 | 14 | 1709 | XP_016875208.1 | |
XM_017019720.1 | 12 | 2787 | XP_016875209.1 | |
AB046815.1 | 9 | 3644 | BAB13421.1 | |
AK131442.1 | ||||
BC030020.2 | 14 | 1761 | AAH30020.1 | |
BC035911.1 | 3 | 666 | AAH35911.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
dgv1566n100 | Chr.12:123610211 - 123711309 on Build GRCh38 | Gain | GTF2H3 DDX55 TCTN2 EIF2B1 |
dgv524e212 | Chr.12:123614065 - 123625575 on Build GRCh38 | Loss | DDX55 EIF2B1 |
nsv1042181 | Chr.12:123552853 - 123668403 on Build GRCh38 | Gain | LOC101927415 GTF2H3 DDX55 TMED2 EIF2B1 |
More Information
Additional Information:
For this assay, SNP(s) [rs78353231] 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 |