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|solute carrier family 25, member 38|
|Locus||Chr. 3 p22.1|
SLC25A38 is a human gene.
- SLC25A38 is involved in mitochondrial handling of glycine and is needed for the first step in heme synthesis. Mutations in this gene can lead to an autosomal recessive form of sideroblastic anemia.
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see also solute carrier disorders
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