Genomic Map
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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 7 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC38A7 | NM_001308384.1 | NP_001295313.1 | ||
| NM_018231.2 | NP_060701.1 | |||
| XM_017023393.1 | XP_016878882.1 | |||
| XM_017023394.1 | XP_016878883.1 | |||
| XM_017023395.1 | XP_016878884.1 | |||
| XM_017023396.1 | XP_016878885.1 | |||
| XM_017023397.1 | XP_016878886.1 | |||
| XM_017023398.1 | XP_016878887.1 | |||
| XM_017023399.1 | 7 | 1153 | XP_016878888.1 | |
| AK001677.1 | BAA91830.1 | |||
| AK022786.1 | BAB14244.1 | |||
| AK222932.1 | BAD96652.1 | |||
| AK299424.1 | ||||
| BC001961.1 | AAH01961.1 | |||
| CR457236.1 | CAG33517.1 |
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
SLC38A7
CNOT1
SNORA46
SNORA50A
|
| 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:
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