SLC25A4 Back

solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4

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NCBI Description of SLC25A4

This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. 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 SLC25A4 Add / Edit SLC25A4: Annotations

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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).


SLC25A4 is highly significantly mutated in
SLC25A4 is significantly mutated in
SLC25A4 is near significance in

Click on a tumor type to see its full list of significant genes.

Data details

Mutation list for SLC25A4