Genomic Map
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Target Gene Details
Entrez Gene ID: | 26053 |
Gene Name: | autism susceptibility candidate 2 |
Gene Aliases: |
FBRSL2, MRD26 |
Location: |
Chr.7:69598475-70793068 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| AUTS2 | NM_001127231.2 | 1 | 132 | NP_001120703.1 |
| NM_001127232.2 | 1 | 132 | NP_001120704.1 | |
| NM_015570.3 | 1 | 132 | NP_056385.1 | |
| XM_011516010.2 | 1 | 576 | XP_011514312.1 | |
| XM_011516011.2 | 1 | 576 | XP_011514313.1 | |
| XM_011516012.2 | 1 | 576 | XP_011514314.1 | |
| XM_011516013.2 | 1 | 576 | XP_011514315.1 | |
| XM_011516014.2 | 1 | 576 | XP_011514316.1 | |
| XM_017011951.1 | 1 | 576 | XP_016867440.1 | |
| BC064693.1 | 1 | 140 | AAH64693.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv428169 | Chr.7:69556496 - 69731757 on Build GRCh38 | Gain |
 AUTS2
LOC100507468
|
| nsv5783 | Chr.7:69583622 - 69601774 on Build GRCh38 | Deletion |
AUTS2
LOC100507468
|
| nsv1076918 | Chr.7:69597713 - 69601614 on Build GRCh38 | Deletion |
AUTS2
|
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Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
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