This gene encodes an integral plasma membrane glycoprotein of the liver, islet beta cells, intestine, and kidney epithelium. The encoded protein mediates facilitated bidirectional glucose transport. Because of its low affinity for glucose, it has been suggested as a glucose sensor. Mutations in this gene are associated with susceptibility to diseases, including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC2A2-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC2A2-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC2A2-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC2A2-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC2A2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes an integral plasma membrane glycoprotein of the liver, islet beta cells, intestine, and kidney epithelium. The encoded protein mediates facilitated bidirectional glucose transport. Because of its low affinity for glucose, it has been suggested as a glucose sensor. Mutations in this gene are associated with susceptibility to diseases, including Fanconi-Bickel syndrome and noninsulin-dependent diabetes mellitus (NIDDM). Alternative splicing results in multiple transcript variants of this gene. [provided by RefSeq, Jul 2013]
Gene Symbol : SLC2A2
Gene Name : Solute carrier family 2 member 2
Chromosome : CHR 3: 171,026,978-170,996,340
Locus : 3q26.2
Alt. Genes : CELA3A
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