LMPD Database

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LMP002285

UniProt Annotations

Entry Information
Gene Namesolute carrier family 25 (carnitine/acylcarnitine translocase), member 20
Protein EntryMCAT_HUMAN
UniProt IDO43772
SpeciesHuman
Comments
Comment typeDescription
DiseaseCarnitine-acylcarnitine translocase deficiency (CACTD) [MIM
FunctionMediates the transport of acylcarnitines of different length across the mitochondrial inner membrane from the cytosol to the mitochondrial matrix for their oxidation by the mitochondrial fatty acid-oxidation pathway.
SimilarityBelongs to the mitochondrial carrier (TC 2.A.29) family.
SimilarityContains 3 Solcar repeats. {ECO
Subcellular LocationMitochondrion inner membrane; Multi-pass membrane protein.