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slc25a38

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Official Full Name
solute carrier family 25, member 38
Background
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.
Synonyms
SLC25A38; solute carrier family 25, member 38; solute carrier family 25 member 38; FLJ20551; FLJ22703