Assay Details
Target Gene Details
Entrez Gene ID: | 6520 |
Gene Name: | solute carrier family 3 member 2 |
Gene Aliases: |
4F2, 4F2HC, 4T2HC, CD98, CD98HC, MDU1, NACAE |
Location: |
Chr.11:62856012-62888883 on Build GRCh38 |
Assay Gene Location: | Within Intron 1 |
Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
---|---|---|---|---|
SLC3A2 | NM_001012662.2 | NP_001012680.1 | ||
NM_001012664.2 | NP_001012682.1 | |||
NM_002394.5 | NP_002385.3 | |||
AK025584.1 | ||||
AU143131.1 | ||||
BC001061.2 | AAH01061.2 | |||
BC003000.1 | AAH03000.2 | |||
BE018712.1 | ||||
BU556953.1 | ||||
BX362778.2 | ||||
CB138799.1 | ||||
CN302816.1 | ||||
DC395235.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
Target Variation |
Location | CNV Subtype |
Genes |
---|---|---|---|
nsv1159903 | Chr.11:62818434 - 62885307 on Build GRCh38 | Duplication | SNORD29 SNORD26 STX5 SNORD25 SNHG1 SNORD31 SLC3A2 RNU2-2P SNORD22 SNORD27 SNORD30 WDR74 LOC105369332 SNORD28 |
esv3626615 | Chr.11:62861292 - 62866965 on Build GRCh38 | Loss | SLC3A2 |
nsv508636 | Chr.11:62779642 - 62876986 on Build GRCh38 | Deletion | SNORD29 TMEM179B SNORD26 TMEM223 STX5 MIR6748 SNORD25 SNHG1 SNORD31 NXF1 SLC3A2 RNU2-2P SNORD22 SNORD27 SNORD30 WDR74 LOC105369332 SNORD28 MIR6514 TAF6L |
More Information
Set Membership: |
Intragenic Intronic Non-exonic DGV Variation |