Genomic Map
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Target Gene Details
Entrez Gene ID: | 151636 |
Gene Name: | deltex E3 ubiquitin ligase 3L |
Gene Aliases: |
BBAP |
Location: |
Chr.3:122564338-122575203 on Build GRCh38 |
Assay Gene Location: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| DTX3L | NM_138287.3 | 5 | 2925 | NP_612144.1 |
| AK056406.1 | 1 | 1234 | ||
| AK093782.1 | 1 | 133 | ||
| AK125086.1 | 5 | 2925 | ||
| AL833598.1 | 5 | 2858 | ||
| BC042191.1 | 5 | 2844 | AAH42191.1 | |
| BX648267.1 | 1 | 3784 | ||
| BX648645.1 | 5 | 2678 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv2672720 | Chr.3:122570146 - 122575337 on Build GRCh38 | Deletion |
 DTX3L
|
| esv3597613 | Chr.3:122570126 - 122575297 on Build GRCh38 | Loss |
DTX3L
|
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Additional Information:
For this assay, SNP(s) [rs73858316] 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
|
Panther Classification:
Gene Ontology Categories:
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