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SLC25A38

Official Full Name
solute carrier family 25 member 38
Organism
Homo sapiens
GeneID
54977
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 (anemia, sideroblastic, 2, pyridoxine-refractory). A related pseudogene is found on chromosome 1. [provided by RefSeq, Aug 2017]
Synonyms
SIDBA2;

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