This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia (anemia, sideroblastic, 2, pyridoxine-refractory). A related pseudogene is found on chromosome 1. [provided by RefSeq, Aug 2017]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| SLC25A38-20-RE | 20 (40 μL) | 200 μL |  |
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| SLC25A38-20-OR | 20 (40 μL) | 200 μL |  |
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| SLC25A38-20-GO | 20 (40 μL) | 200 μL |  |
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| SLC25A38-20-GR | 20 (40 μL) | 200 μL |  |
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| SLC25A38-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene is a member of the mitochondrial carrier family. The encoded protein is required during erythropoiesis and is important for the biosynthesis of heme. Mutations in this gene are the cause of autosomal congenital sideroblastic anemia (anemia, sideroblastic, 2, pyridoxine-refractory). A related pseudogene is found on chromosome 1. [provided by RefSeq, Aug 2017]
Gene Symbol : SLC25A38
Gene Name : Solute carrier family 25 member 38
Chromosome : CHR 3: 393,833,23-393,973,27
Locus : 3p22.1
Alt. Genes : LRPPRC
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