SCUBA

ACADM — Acyl-CoA dehydrogenase medium chain

ACADM belongs to a gene co-expression module in 3 of 28 SCUBA cell types. Each module groups genes that rise and fall together in that cell type; the genes it shares a module with are its closest co-expression partners there.

ACADM's module in each cell type

Cell typeModuleShares the module with
Gamma-delta T cellsMitoribosome Small Subunit
Mitochondrial & OxPhos
C14orf119, CHCHD1, COA3, COA4, COMMD8, GALK1, GEMIN6, ISCA2 +24 more
Innate lymphoid cellsRNA Chromatin Regulation
RNA processing & translation
AURKAIP1, BUD23, CBX3, CMC2, COPB1, DNAJA2, DYNC1LI1, G3BP1 +19 moreView in SCUBA
MacrophagesOxidative Metabolic Program
Mitochondrial & OxPhos
CA2, CALM3, CAPG, COQ2, CSRP1, CSTB, DENND2D, EIF4EBP1 +29 moreView in SCUBA

About the gene

SynonymsACAD1, MCAD, MCADH
Chromosome1: 75724431-75787575
Predicted locationIntracellular
Essential geneNo
Protein classDisease related genes, Enzymes, Human disease related genes, Metabolic proteins, Potential drug targets, Predicted intracellular proteins
Molecular functionOxidoreductase
Biological processFatty acid metabolism, Lipid metabolism

Function

Medium-chain specific acyl-CoA dehydrogenase is one of the acyl-CoA dehydrogenases that catalyze the first step of mitochondrial fatty acid beta-oxidation, an aerobic process breaking down fatty acids into acetyl-CoA and allowing the production of energy from fats. The first step of fatty acid beta-oxidation consists in the removal of one hydrogen from C-2 and C-3 of the straight-chain fatty acyl-CoA thioester, resulting in the formation of trans-2-enoyl-CoA. Electron transfer flavoprotein (ETF) is the electron acceptor that transfers electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase). Among the different mitochondrial acyl-CoA dehydrogenases, medium-chain specific acyl-CoA dehydrogenase acts specifically on acyl-CoAs with saturated 6 to 12 carbons long primary chains.

Human Protein Atlas · Open Targets · UniProt

Gene annotation from the Human Protein Atlas and UniProt; see sources & licences.