SLC25A22 Back

solute carrier family 25 (mitochondrial carrier: glutamate), member 22

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NCBI Description of SLC25A22
This gene encodes a mitochondrial glutamate carrier. Mutations in this gene are associated with early infantile epileptic encephalopathy. Multiple alternatively spliced variants, encoding the same protein, have been identified.

Community Annotation of SLC25A22 Add / Edit SLC25A22: Annotations

No community annotations yet for SLC25A22.
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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

SLC25A22 is highly significantly mutated in
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SLC25A22 is significantly mutated in
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SLC25A22 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 SLC25A22