Assay Details
Target Gene Details
Entrez Gene ID: | 92737 |
Gene Name: | delta/notch like EGF repeat containing |
Gene Aliases: |
UNQ26, bet |
Location: |
Chr.2:229357629-229714570 on Build GRCh38 |
Assay Gene Location: | Within Exon 13 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
DNER | NM_139072.3 | 13 | 3007 | NP_620711.3 |
XM_005246950.2 | 12 | 2871 | XP_005247007.1 | |
AL137311.1 | 6 | 1405 | CAB70690.1 | |
AY358891.1 | 13 | 2970 | AAQ89250.1 | |
BC024766.2 | 9 | 2013 | AAH24766.2 | |
BC035009.1 | 13 | 2997 | AAH35009.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv834564 | Chr.2:229239150 - 229431420 on Build GRCh38 | Gain | DNER PID1 |
nsv3198 | Chr.2:229341777 - 229372836 on Build GRCh38 | Insertion | DNER |
esv3594572 | Chr.2:229347352 - 229417034 on Build GRCh38 | Loss | DNER |
More Information
Additional Information:
For this assay, SNP(s) [rs78060918] 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 |