Name

SLC25A20 Gene

solute carrier family 25 (carnitine/acylcarnitine translocase), member 20

This gene product is one of several closely related mitochondrial-membrane carrier proteins that shuttle substrates between cytosol and the intramitochondrial matrix space. This protein mediates the transport of acylcarnitines into mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway. Mutations in this gene are associated with carnitine-acylcarnitine translocase deficiency, which can cause a variety of pathological conditions such as hypoglycemia, cardiac arrest, hepatomegaly, hepatic dysfunction and muscle weakness, and is usually lethal in new born and infants. [provided by RefSeq, Jul 2008]

SLC25A20P1 Gene

solute carrier family 25 (carnitine/acylcarnitine translocase), member 20 pseudogene 1

slc25a20 Gene Set

From GeneRIF Biological Term Annotations

genes co-occuring with the biological term slc25a20 in literature-supported statements describing functions of genes from the GeneRIF Biological Term Annotations dataset.

SLC25A20 Gene Set

From Pathway Commons Protein-Protein Interactions

interacting proteins for SLC25A20 from the Pathway Commons Protein-Protein Interactions dataset.