Genomic Map
Back To TopAssay Details
Target Gene Details
Entrez Gene ID: | 6767 |
Gene Name: | suppression of tumorigenicity 13 (colon carcinoma) (Hsp70 interacting protein) |
Gene Aliases: |
AAG2, FAM10A1, FAM10A4, HIP, HOP, HSPABP, HSPABP1, P48, PRO0786, SNC6 |
Location: |
Chr.22:40824535-40857008 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 9 - Exon 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ST13 | NM_001278589.1 | NP_001265518.1 | ||
| NM_003932.4 | NP_003923.2 | |||
| AK130770.1 | ||||
| AK303530.1 | ||||
| AK312399.1 | ||||
| AK316155.1 | ||||
| AY513286.1 | AAT08039.1 | |||
| AY826824.1 | ||||
| AY826825.1 | ||||
| BC052982.1 | AAH52982.1 | |||
| BC071629.1 | AAH71629.1 | |||
| BC107148.1 | AAI07149.1 | |||
| BC121107.1 | ||||
| BC121108.1 | ||||
| BC139724.1 | ||||
| CR456586.1 | CAG30472.1 | |||
| U17714.1 | AAC97526.1 | |||
| U28918.1 | AAB38382.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv834206 | Chr.22:40696722 - 40838881 on Build GRCh38 | Gain |
 ST13
SLC25A17
MIR4766
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
Back To Top