Genomic Map
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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 14 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| SLC3A2 | NM_001012662.2 | 12 | 1849 | NP_001012680.1 |
| NM_001012664.2 | 10 | 1660 | NP_001012682.1 | |
| NM_001013251.2 | 9 | 1437 | NP_001013269.1 | |
| NM_002394.5 | 12 | 1846 | NP_002385.3 | |
| NR_037193.1 | 9 | 1179 | ||
| AA594112.1 | 1 | 504 | ||
| AB018010.1 | 9 | 1396 | BAA84649.1 | |
| AF055031.1 | 9 | 1149 | ||
| AK025584.1 | 12 | 1750 | ||
| AK090758.1 | ||||
| AK094620.1 | 6 | 1704 | ||
| AK225304.1 | 9 | 1384 | ||
| AK304497.1 | 10 | 1355 | ||
| AK308797.1 | ||||
| BC001061.2 | 12 | 1756 | AAH01061.2 | |
| BC003000.1 | 10 | 1528 | AAH03000.2 | |
| BQ128156.1 | 1 | 508 | ||
| CA453972.1 | 4 | 369 | ||
| J02769.1 | 9 | 1338 | AAA51540.1 | |
| J02939.1 | 9 | 1394 | AAA52497.1 | |
| J03569.1 | 9 | 1423 | AAA35536.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv34011 | Chr.11:62885307 - 63226230 on Build GRCh38 | Loss |
 SLC22A6
SLC3A2
SLC22A25
CHRM1
SLC22A24
SLC22A8
|
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Additional Information:
For this assay, SNP(s) [rs76688902] 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:
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