The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC35A1-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC35A1-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC35A1-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC35A1-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC35A1-20-AQ | 20 (40 μL) | 200 μL |  |
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The protein encoded by this gene is found in the membrane of the Golgi apparatus, where it transports nucleotide sugars into the Golgi. One such nucleotide sugar is CMP-sialic acid, which is imported into the Golgi by the encoded protein and subsequently glycosylated. Defects in this gene are a cause of congenital disorder of glycosylation type 2F (CDG2F). Two transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Dec 2009]
Gene Symbol : SLC35A1
Gene Name : Solute carrier family 35 member A1
Chromosome : CHR 6: 874,729,24-875,123,38
Locus : 6q15
Alt. Genes : RAD50
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