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Solute carrier family 25 (mitochondrial carrier; citrate transporter), member 1 (HGNC Symbol)
Entrez gene summary
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]
P53007 [Direct mapping] Tricarboxylate transport protein, mitochondrial
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Transporters Electrochemical Potential-driven transporters MEMSAT3 predicted membrane proteins MEMSAT-SVM predicted membrane proteins SPOCTOPUS predicted membrane proteins Predicted intracellular proteins Disease related genes Potential drug targets Protein evidence (Kim et al 2014) Protein evidence (Ezkurdia et al 2014)
B4DP62 [Direct mapping] Solute carrier family 25 (Mitochondrial carrier citrate transporter), member 1, isoform CRA_b; Tricarboxylate transport protein, mitochondrial; cDNA FLJ60026, highly similar to Tricarboxylate transport protein, mitochondrial
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MEMSAT3 predicted membrane proteins MEMSAT-SVM predicted membrane proteins SPOCTOPUS predicted membrane proteins Phobius predicted secreted proteins Predicted intracellular proteins Protein evidence (Ezkurdia et al 2014)