Assay Details
Target Gene Details
Entrez Gene ID: | 161582 |
Gene Name: | dyslexia susceptibility 1 candidate 1 |
Gene Aliases: |
CILD25, DNAAF4, DYX1, DYXC1, EKN1, RD |
Location: |
Chr.15:55417755-55508234 on Build GRCh38 |
Assay Gene Location: | Within Intron 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DYX1C1 | NM_001033559.2 | NP_001028731.1 | ||
| NM_001033560.1 | NP_001028732.1 | |||
| NM_130810.3 | NP_570722.2 | |||
| AF337549.1 | AAL73230.1 | |||
| AK095201.1 | BAC04498.1 | |||
| AK302316.1 | ||||
| BC062564.1 | AAH62564.1 | |||
| KU178882.1 | ||||
| KU178883.1 | ||||
| KU178884.1 |
Target Gene Details
Entrez Gene ID: | 100533483 |
Gene Name: | DYX1C1-CCPG1 readthrough (NMD candidate) |
Gene Aliases: |
- |
Location: |
Chr.15:55355223-55498584 on Build GRCh38 |
Assay Gene Location: | Within Intron 3 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DYX1C1-CCPG1 | NR_037923.1 | |||
| AK295788.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2761899 | Chr.15:53592144 - 55643724 on Build GRCh38 | Gain+Loss |
|
| esv3636565 | Chr.15:55484284 - 55490748 on Build GRCh38 | Loss |
|
| nsv1542 | Chr.15:55461944 - 55496407 on Build GRCh38 | Insertion |
|
| nsv569523 | Chr.15:55263404 - 55544506 on Build GRCh38 | Gain |
|
| nsv1043789 | Chr.15:55108674 - 55800256 on Build GRCh38 | Gain |
|
| nsv569539 | Chr.15:55430015 - 55963576 on Build GRCh38 | Loss |
|
| nsv833016 | Chr.15:55456971 - 55605708 on Build GRCh38 | Gain |
|
More Information
Set Membership: |
|

Genomic Map