SLC25A26, solute carrier family 25 member 26

SLC25A26, solute carrier family 25 member 26

• This gene is a member of the mitochondrial carrier family which includes nuclear-encoded transporters localized on the inner mitochondrial membranes. Members of the family transport important small molecules across the mitochondrial inner membrane. This protein is involved in the transport of S-adenosylmethionine (SAM) into the mitochondria. Mutations in this gene are associated with combined oxidative phosphorylation deficiency 28. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Apr 2017]

• Gene Synonyms (COXPD28, SAMC, S-adenosylmethionine mitochondrial carrier protein, mitochondrial S-adenosylmethionine transporter, solute carrier family 25 (S-adenosylmethionine carrier), member 26, solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 26,)
• NCBI Gene ID: 115286
• Species: Homo sapiens (Human)
• UNIPROT ID#>>F8WAB8
  UNIPROT ID#>>Q70HW3
• View the NCBI Database for this Gene »

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 26 interacts with:

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