This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC16A12-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC16A12-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC16A12-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC16A12-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC16A12-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010]
Gene Symbol : SLC16A12
Gene Name : Solute carrier family 16 member 12
Chromosome : CHR 10: 895,360,27-894,302,93
Locus : 10q23.31
Alt. Genes : LRPPRC
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