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SLC25A1, solute carrier family 25 member 1

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SLC25A1, solute carrier family 25 member 1

  • This gene encodes a member of the mitochondrial carrier subfamily of solute carrier proteins. Members of this family include nuclear-encoded transporters that translocate small metabolites across the mitochondrial membrane. This protein regulates the movement of citrate across the inner membranes of the mitochondria. Mutations in this gene have been associated with combined D-2- and L-2-hydroxyglutaric aciduria. Pseudogenes of this gene have been identified on chromosomes 7, 11, 16, and 19. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2013]

  • Gene Synonyms (tricarboxylate transport protein, mitochondrial, citrate transport protein, solute carrier family 20 (mitochondrial citrate transporter), member 3, solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1, tricarboxylate carrier protein, CMS23, CTP, D2L2AD, SEA, SLC20A3,)
  • NCBI Gene ID: 6576
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>B4DP62
    UNIPROT ID#>>P53007
    UNIPROT ID#>>D9HTE9
  • 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 1 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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