This gene is highly expressed in the liver and is inducible by manganese. Its protein product appears to be critical in maintaining manganese levels, and has higher specificity for manganese than zinc. Loss of function mutations appear to result in a pleomorphic phenotype, including dystonia and adult-onset parkinsonism. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Mar 2012]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC30A10-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC30A10-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC30A10-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC30A10-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC30A10-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is highly expressed in the liver and is inducible by manganese. Its protein product appears to be critical in maintaining manganese levels, and has higher specificity for manganese than zinc. Loss of function mutations appear to result in a pleomorphic phenotype, including dystonia and adult-onset parkinsonism. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Mar 2012]
Gene Symbol : SLC30A10
Gene Name : Solute carrier family 30 member 10
Chromosome : CHR 1: 219,959,753-219,910,397
Locus : 1q41
Alt. Genes : CEBPZ
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