Assay Details
Target Gene Details
Entrez Gene ID: | 138009 |
Gene Name: | DDB1 and CUL4 associated factor 4 like 2 |
Gene Aliases: |
WDR21C |
Location: |
Chr.8:87870743-87874068 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DCAF4L2 | NM_152418.3 | 1 | 3030 | NP_689631.1 |
AL833507.1 | 1 | 2978 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv831384 | Chr.8:87734490 - 87905020 on Build GRCh38 | Gain | DCAF4L2 |
nsv611709 | Chr.8:86701747 - 87889581 on Build GRCh38 | Gain | CNGB3 CNBD1 DCAF4L2 |
nsv831385 | Chr.8:87795034 - 87953244 on Build GRCh38 | Loss | DCAF4L2 |
More Information
Additional Information:
For this assay, SNP(s) [rs200647910,rs529590827] 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 |