Genomic Map
Back To TopAssay 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: | Overlaps Exon 1 - 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 |
 SNORD31
SNORD28
SNORD29
STX5
RNU2-2P
WDR74
SNORD22
SNORD25
SNORD30
LOC105369332
SNORD27
SNHG1
SNORD26
SLC3A2
|
| nsv508636 | Chr.11:62779642 - 62876986 on Build GRCh38 | Deletion |
SNORD31
TMEM223
SNORD28
SNORD29
STX5
NXF1
TMEM179B
RNU2-2P
WDR74
SNORD22
SNORD25
SNORD30
TAF6L
MIR6514
LOC105369332
MIR6748
SNORD27
SNHG1
SNORD26
SLC3A2
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
Back To Top