SLC25A38 Back

solute carrier family 25, member 38

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NCBI Description of SLC25A38

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.

Community Annotation of SLC25A38 Add / Edit SLC25A38: Annotations

No community annotations yet for SLC25A38.
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Figure notes


• "Mouse over" a mutation to see details.
• Missense green saturation indicates evolutionary conservation of the mutated positions.
• Red hashes in protein strip are splice sites.
• Blue-white-red bars are log2 copy ratio distributions (–1 to +1) from Zack et al. (2013).


Legend

SLC25A38 is highly significantly mutated in
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SLC25A38 is significantly mutated in
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SLC25A38 is near significance in
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Click on a tumor type to see its full list of significant genes.

Data details


Mutation list for SLC25A38