This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC6A19-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC6A19-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC6A19-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC6A19-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC6A19-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a system B(0) transmembrane protein that actively transports most neutral amino acids across the apical membrane of epithelial cells. Mutations in this gene result in Hartnup disorder. [provided by RefSeq, Jul 2008]
Gene Symbol : SLC6A19
Gene Name : Solute carrier family 6 member 19
Chromosome : CHR 5: 120,159,4-122,511,6
Locus : 5p15.33
Alt. Genes : ARPC2
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