SLC25A16 Back

solute carrier family 25 (mitochondrial carrier; Graves disease autoantigen), member 16

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NCBI Description of SLC25A16
This gene encodes a protein that contains three tandemly repeated mitochondrial carrier protein domains. The encoded protein is localized in the inner membrane and facilitates the rapid transport and exchange of molecules between the cytosol and the mitochondrial matrix space. This gene has a possible role in Graves' disease. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.

Community Annotation of SLC25A16 Add / Edit SLC25A16: Annotations

No community annotations yet for SLC25A16.
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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

SLC25A16 is highly significantly mutated in
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SLC25A16 is significantly mutated in
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SLC25A16 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 SLC25A16