Assay Details
Target Gene Details
Entrez Gene ID: | 55238 |
Gene Name: | solute carrier family 38 member 7 |
Gene Aliases: |
SNAT7 |
Location: |
Chr.16:58665109-58684777 on Build GRCh38 |
Assay Gene Location: | Within Exon 2 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC38A7 | NM_001308384.1 | 2 | 813 | NP_001295313.1 |
NM_018231.2 | 3 | 345 | NP_060701.1 | |
XM_017023393.1 | 2 | 826 | XP_016878882.1 | |
XM_017023394.1 | 3 | 321 | XP_016878883.1 | |
XM_017023395.1 | 3 | 321 | XP_016878884.1 | |
XM_017023396.1 | 3 | 321 | XP_016878885.1 | |
XM_017023397.1 | 3 | 321 | XP_016878886.1 | |
XM_017023398.1 | 3 | 321 | XP_016878887.1 | |
XM_017023399.1 | 3 | 321 | XP_016878888.1 | |
AK001677.1 | 3 | 338 | BAA91830.1 | |
AK022786.1 | 3 | 311 | BAB14244.1 | |
AK222932.1 | 3 | 307 | BAD96652.1 | |
AK299424.1 | ||||
BC001961.1 | 2 | 294 | AAH01961.1 | |
CR457236.1 | CAG33517.1 | |||
HY021779.1 | 3 | 346 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv510686 | Chr.16:58612215 - 58731990 on Build GRCh38 | Deletion | GOT2 SLC38A7 CNOT1 |
esv2758650 | Chr.16:58545101 - 58842133 on Build GRCh38 | Loss | GOT2 SNORA46 SNORA50A SLC38A7 CNOT1 |
nsv528513 | Chr.16:58638859 - 58683970 on Build GRCh38 | Loss | SLC38A7 |
More Information
Set Membership: |
Intragenic Exonic DGV Variation |