This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC17A5-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC17A5-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC17A5-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC17A5-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC17A5-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a membrane transporter that exports free sialic acids that have been cleaved off of cell surface lipids and proteins from lysosomes. Mutations in this gene cause sialic acid storage diseases, including infantile sialic acid storage disorder and and Salla disease, an adult form. [provided by RefSeq, Jul 2008]
Gene Symbol : SLC17A5
Gene Name : Solute carrier family 17 member 5
Chromosome : CHR 6: 736,540,13-735,933,77
Locus : 6q13
Alt. Genes : OPTN
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