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SLC25A12, solute carrier family 25 member 12

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SLC25A12, solute carrier family 25 member 12

  • This gene encodes a calcium-binding mitochondrial carrier protein. The encoded protein localizes to the mitochondria and is involved in the exchange of aspartate for glutamate across the inner mitochondrial membrane. Polymorphisms in this gene may be associated with autism, and mutations in this gene may also be a cause of global cerebral hypomyelination. Alternatively spliced transcript variants have been observed for this gene. [provided by RefSeq, Apr 2012]

  • Gene Synonyms (calcium-binding mitochondrial carrier protein Aralar1, araceli hiperlarga, calcium binding mitochondrial carrier superfamily member Aralar1, mitochondrial aspartate glutamate carrier 1, solute carrier family 25 (aspartate/glutamate carrier), member 12, solute carrier family 25 (mitochondrial carrier, Aralar), member 12, AGC1, ARALAR, EIEE39,)
  • NCBI Gene ID: 8604
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>O75746
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

solute carrier family 25 member 12 interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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