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: | Within Exon 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC3A2 | NM_001012662.2 | 4 | 860 | NP_001012680.1 |
| NM_001012664.2 | 2 | 671 | NP_001012682.1 | |
| NM_001013251.2 | 1 | 448 | NP_001013269.1 | |
| NM_002394.5 | 4 | 857 | NP_002385.3 | |
| AB018010.1 | 1 | 407 | BAA84649.1 | |
| AK025584.1 | 4 | 761 | ||
| AK090758.1 | ||||
| AK225304.1 | 1 | 395 | ||
| AK304497.1 | ||||
| AK304685.1 | ||||
| AU143131.1 | 3 | 727 | ||
| BC001061.2 | 4 | 767 | AAH01061.2 | |
| BC003000.1 | 2 | 539 | AAH03000.2 | |
| BU556953.1 | ||||
| BX362778.2 | 4 | 824 | ||
| BX443653.2 | 1 | 448 | ||
| CB151304.1 | 1 | 505 | ||
| J02769.1 | 1 | 349 | AAA51540.1 | |
| J02939.1 | 1 | 405 | AAA52497.1 | |
| J03569.1 | 1 | 432 | AAA35536.1 |
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 |
 SNORD22
SNORD27
LOC105369332
RNU2-2P
SNORD30
SNORD31
WDR74
SNORD29
SLC3A2
SNORD28
STX5
SNHG1
SNORD25
SNORD26
|
Back To TopMore Information
Additional Information:
For this assay, SNP(s) [rs73487878] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Gene Ontology Categories:
Back To Top