This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2010]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC11A2-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC11A2-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC11A2-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC11A2-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC11A2-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the solute carrier family 11 protein family. The product of this gene transports divalent metals and is involved in iron absorption. Mutations in this gene are associated with hypochromic microcytic anemia with iron overload. A related solute carrier family 11 protein gene is located on chromosome 2. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Apr 2010]
Gene Symbol : SLC11A2
Gene Name : Solute carrier family 11 member 2
Chromosome : CHR 12: 510,283,34-509,522,62
Locus : 12q13.12
Alt. Genes : RASA4
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