SLC25A26

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]

Description

solute carrier family 25 member 26

Protein family

Disease related genes, Mapped to neXtProt, Mapped to UniProt SWISS-PROT, Potential drug targets, Predicted intracellular proteins, Predicted membrane proteins, Protein evidence (Peptideatlas), Transporters

Chromosome

3:p14.1 (66133610 - 66388116)

Ensembl ID

ENSG00000144741  (ver. 99.38)

Orthologs

Mouse Slc25a26: ENSMUSG00000045100

UniProt

Q70HW3

neXtProt

NX_Q70HW3

Human splice variants
Mouse splice variants