QuickView for SLC25A38;jsessionid=155F6D6292E4417B9F92AF0DAD870A37 (gene)

Gene Symbol:

SLC25A38 Homo sapiens

Full name:

solute carrier family 25 member 38

Synonyms:

SIDBA2, solute carrier family 25 member 38, appoptosin

Genomic Location:

Chr 3: 39399819-39413823

Description:

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.

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.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Saccharomyces cerevisiae ,  Macaca mulatta ,  Schizosaccharomyces pombe ,  Gallus gallus ,  Pan troglodytes ,  Canis lupus familiaris ,  Bos taurus ,  Danio rerio

External Links:

Entrez Gene

Transcription Factor
Binding Sites:

SCGGAAGY_ELK1_02 ,  EGR1_01

Cytogenetic Map:

3p22.1

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