Genomic Map
Back To TopAssay 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 12 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC38A7 | NM_001308384.1 | 8 | 3888 | NP_001295313.1 |
| NM_018231.2 | 12 | 3823 | NP_060701.1 | |
| XM_017023393.1 | 11 | 4304 | XP_016878882.1 | |
| XM_017023394.1 | 9 | 3396 | XP_016878883.1 | |
| XM_017023395.1 | 11 | 3599 | XP_016878884.1 | |
| XM_017023396.1 | 10 | 3451 | XP_016878885.1 | |
| AI201677.1 | 1 | 256 |
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 |
 CNOT1
GOT2
SLC38A7
|
| esv2758650 | Chr.16:58545101 - 58842133 on Build GRCh38 | Loss |
CNOT1
SNORA50A
GOT2
SNORA46
SLC38A7
|
| nsv528513 | Chr.16:58638859 - 58683970 on Build GRCh38 | Loss |
SLC38A7
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
Back To Top