This gene encodes a type II membrane glycoprotein which is one of the components of the renal amino acid transporter which transports neutral and basic amino acids in the renal tubule and intestinal tract. Mutations and deletions in this gene are associated with cystinuria. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC3A1-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC3A1-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC3A1-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC3A1-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC3A1-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a type II membrane glycoprotein which is one of the components of the renal amino acid transporter which transports neutral and basic amino acids in the renal tubule and intestinal tract. Mutations and deletions in this gene are associated with cystinuria. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Gene Symbol : SLC3A1
Gene Name : Solute carrier family 3 member 1
Chromosome : CHR 2: 442,754,57-443,208,23
Locus : 2p21
Alt. Genes : KIF20A
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