Acadvl - acyl-Coenzyme A dehydrogenase, very long chain Gene
Also Known as vlcad
Species: Mus musculus
Summary
This gene encodes a homodimeric mitochondrial flavoprotein and is a member of the acyl-CoA dehydrogenase family. Members of this family catalyze the first step of fatty acid beta-oxidation, forming a C2-C3 trans-double bond in a FAD-dependent reaction. As beta-oxidation cycles through its four steps, each member of the acyl-CoA dehydrogenase family works at an optimum fatty acid chain-length. This enzyme has its optimum length between C16- and C20-acylCoA and localizes to the inner mitochondrial membrane (unlike related acyl-CoA dehydrogenases). In mice, deficiency of this gene can cause ventricular arrhythmias as well as fasting and cold intolerance. [provided by RefSeq, Nov 2012]
Acadvl Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_017366.3 | NP_059062.1 | very long-chain specific acyl-CoA dehydrogenase, mitochondrial precursor |
| Biological Process GO Annotation | Evidence | References | Source |
|---|---|---|---|
| involved in fatty acid beta-oxidation using acyl-CoA dehydrogenase |
IMP
IMP: Inferred from mutant phenotype
|
15639194 | MGI |
| acts upstream of or within fatty acid catabolic process |
IMP
IMP: Inferred from mutant phenotype
|
21151927 | MGI |
| involved in negative regulation of fatty acid biosynthetic process |
IMP
IMP: Inferred from mutant phenotype
|
15639194 | MGI |
| involved in negative regulation of fatty acid oxidation |
IMP
IMP: Inferred from mutant phenotype
|
15639194 | MGI |
| involved in regulation of cholesterol metabolic process |
IMP
IMP: Inferred from mutant phenotype
|
15639194 | MGI |
| acts upstream of or within response to cold |
IMP
IMP: Inferred from mutant phenotype
|
21151927 | MGI |
| involved in temperature homeostasis |
IMP
IMP: Inferred from mutant phenotype
|
15639194 | MGI |
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
very long-chain specific acyl-CoA dehydrogenase, mitochondrial |
|