This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC52A3-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC52A3-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC52A3-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC52A3-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC52A3-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012]
Gene Symbol : SLC52A3
Gene Name : Solute carrier family 52 member 3
Chromosome : CHR 20: 775,984-760,079
Locus : 20p13
Alt. Genes : KIF20A
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