Assay Details
Target Gene Details
Entrez Gene ID: | 120863 |
Gene Name: | DEP domain containing 4 |
Gene Aliases: |
DEP.4 |
Location: |
Chr.12:100203669-100268094 on Build GRCh38 |
Assay Gene Location: | Within Intron 11 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DEPDC4 | NR_135073.1 | |||
| XM_011537876.2 | XP_011536178.1 | |||
| XM_017018779.1 | XP_016874268.1 | |||
| XM_017018780.1 | XP_016874269.1 | |||
| XM_017018782.1 | XP_016874271.1 | |||
| XM_017018783.1 | XP_016874272.1 | |||
| XM_017018784.1 | XP_016874273.1 | |||
| AK090824.1 | BAC03525.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv1048784 | Chr.12:100058759 - 100251225 on Build GRCh38 | Gain |
|
| esv3630550 | Chr.12:100215678 - 100242288 on Build GRCh38 | Gain |
|
| nsv559964 | Chr.12:99872025 - 100538490 on Build GRCh38 | Gain |
|
More Information
Additional Information:
For this assay, SNP(s) [rs76759432] 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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Genomic Map