Genomic Map
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Target Gene Details
Entrez Gene ID: | 89849 |
Gene Name: | autophagy related 16 like 2 |
Gene Aliases: |
ATG16B, WDR80 |
Location: |
Chr.11:72814406-72843740 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 7 - Exon 8 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ATG16L2 | NM_001318766.1 | NP_001305695.1 | ||
| NM_033388.1 | NP_203746.1 | |||
| XM_005274376.4 | XP_005274433.1 | |||
| XM_006718732.2 | XP_006718795.1 | |||
| XM_006718733.3 | XP_006718796.1 | |||
| XM_006718734.2 | XP_006718797.1 | |||
| XM_011545332.1 | XP_011543634.1 | |||
| XM_011545333.1 | XP_011543635.1 | |||
| XM_011545334.1 | XP_011543636.1 | |||
| AK024423.1 | 2 | 459 | BAB15713.1 | |
| AK090597.1 | BAC03485.1 | |||
| AK091151.1 | 6 | 1183 | ||
| AK093017.1 | BAC04021.1 | |||
| AK303270.1 | ||||
| BC036713.2 | AAH36713.1 | |||
| BC137489.1 | ||||
| BC137490.1 | ||||
| BC142718.1 | ||||
| BC146660.1 | ||||
| BQ929430.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv951039 | Chr.11:72816356 - 72832855 on Build GRCh38 | Deletion |
 ATG16L2
|
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Additional Information:
For this assay, SNP(s) [rs139902397] 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
|
Gene Ontology Categories:
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