| ACADVL |
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| Identifiers |
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| Aliases | ACADVL, acyl-CoA dehydrogenase, very long chain, ACAD6, LCACD, VLCAD, acyl-CoA dehydrogenase very long chain |
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| External IDs | OMIM: 609575; MGI: 895149; HomoloGene: 5; GeneCards: ACADVL; OMA:ACADVL - orthologs |
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| Gene location (Mouse) |
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| | Chr. | Chromosome 11 (mouse) |
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| | Band | 11 B3|11 42.96 cM | Start | 69,901,009 bp |
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| End | 69,906,237 bp |
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| RNA expression pattern |
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| Bgee | | Human | Mouse (ortholog) |
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| Top expressed in | - right adrenal cortex
- apex of heart
- left adrenal cortex
- anterior pituitary
- right lobe of liver
- right hemisphere of cerebellum
- left lobe of thyroid gland
- right lobe of thyroid gland
- left ventricle
- mucosa of transverse colon
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| | Top expressed in | - myocardium of ventricle
- right ventricle
- cardiac muscles
- extraocular muscle
- digastric muscle
- soleus muscle
- intercostal muscle
- sternocleidomastoid muscle
- masseter muscle
- thoracic diaphragm
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| | More reference expression data |
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| BioGPS | |
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| Wikidata |
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Very long-chain specific acyl-CoA dehydrogenase, mitochondrial (VLCAD) is an enzyme that in humans is encoded by the ACADVL gene.
Mutations in the ACADVL are associated with very long-chain acyl-coenzyme A dehydrogenase deficiency. The protein encoded by this gene is targeted to the inner mitochondrial membrane, where it catalyzes the first step of the mitochondrial fatty acid beta-oxidation pathway. This acyl-Coenzyme A dehydrogenase is specific to long-chain and very-long-chain fatty acids. A deficiency in this gene product reduces myocardial fatty acid beta-oxidation and is associated with cardiomyopathy. Alternative splicing results in multiple transcript variants encoding different isoforms.