Genomic Map
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Target Gene Details
Entrez Gene ID: | 51428 |
Gene Name: | DEAD-box helicase 41 |
Gene Aliases: |
ABS, MPLPF |
Location: |
Chr.5:177511577-177517326 on Build GRCh38 |
Assay Gene Location: | Within Exon 15 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DDX41 | NM_001321732.1 | 15 | 2335 | NP_001308661.1 |
| NM_001321830.1 | 16 | 2127 | NP_001308759.1 | |
| NM_016222.3 | 16 | 2058 | NP_057306.2 | |
| AF195417.1 | 16 | 1675 | AAF04150.1 | |
| AK001255.1 | 16 | 1683 | BAA91585.1 | |
| AK026117.1 | 9 | 1000 | ||
| AK027768.1 | 16 | 1693 | BAB55355.1 | |
| AK091545.1 | ||||
| AK091774.1 | 15 | 1970 | ||
| AK092585.1 | 12 | 2545 | ||
| AK222598.1 | 16 | 1683 | BAD96318.1 | |
| AK315491.1 | 16 | 1693 | ||
| AL137455.1 | 6 | 532 | CAB70746.1 | |
| BC015476.1 | 16 | 1698 | AAH15476.1 | |
| BX641072.1 | 14 | 1741 | CAE46035.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv5147 | Chr.5:177511195 - 177556017 on Build GRCh38 | Deletion |
 FAM193B
DDX41
|
| nsv1161311 | Chr.5:177305104 - 177546474 on Build GRCh38 | Duplication |
LMAN2
PRELID1
DBN1
F12
PFN3
PRR7-AS1
FAM193B
RGS14
SLC34A1
PDLIM7
MXD3
PRR7
DOK3
DDX41
GRK6
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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