Ivd Gene Summary [Mouse]
Predicted to enable 3-methylbutanoyl-CoA dehydrogenase activity and identical protein binding activity. Predicted to be involved in L-leucine catabolic process and fatty acid beta-oxidation using acyl-CoA dehydrogenase. Located in mitochondrion. Is expressed in several structures, including alimentary system; brain; ear; genitourinary system; and respiratory system. Human ortholog(s) of this gene implicated in amino acid metabolic disorder and isovaleric acidemia. Orthologous to human IVD (isovaleryl-CoA dehydrogenase). [provided by Alliance of Genome Resources, Jul 2025]
Details
| Type | Protein Coding |
| Official Symbol | Ivd |
| Official Name | isovaleryl coenzyme A dehydrogenase [Source:MGI Symbol;Acc:MGI:1929242] |
| Ensembl ID | ENSMUSG00000027332 |
| Bio databases IDs | |
| Aliases | isovaleryl coenzyme A dehydrogenase |
| Synonyms | 1300016K07Rik, 6720455E18Rik, ACAD2, Isovaleryl-Coa Dehydrogenase, isovaleryl coenzyme A dehydrogenase, Ivd2, IVDH |
| Species | Mouse, Mus musculus |
| Orthologies |
Protein Domains
A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in mouse Ivd often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
- Acyl-CoA dehydrogenase, C-terminal domain
- acyl-CoA dehydrogenase
- Acyl-CoA dehydrogenase, middle domain
- isovaleryl-CoA dehydrogenase
- enzyme
- protein binding
- identical protein binding
- oxidoreductase acting on the CH-CH group of donors with flavin as acceptor
- Acyl-CoA dehydrogenase, N-terminal domain
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
- isovaleryl-coa dehydrogenase deficiency
- colorectal cancer
- hepatocellular carcinoma
- liver cancer
- epithelial cancer
- interstitial lung disease
- idiopathic pulmonary fibrosis
- pervasive developmental disorder
- hereditary disorder
- Parkinson disease
regulates
- branched chain amino acids
- leucine
Subcellular Expression
Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
- Cytoplasm
- Mitochondria
- mitochondrial membrane
- mitochondrial matrix
- nucleoplasm
Gene Ontology Annotations
Describes the biological processes, cellular components, and molecular functions associated with the mouse Ivd gene, providing context for its role in the cell.
Biological Process
Functions and activities the gene product is involved in
- fatty acid beta-oxidation using acyl-CoA dehydrogenase
- branched chain family amino acid catabolic process
- leucine catabolic process
Cellular Component
Where in the cell the gene product is active
- mitochondrial matrix
- mitochondrion
- nucleoplasm
Molecular Function
What the gene product does at the molecular level
- isovaleryl-CoA dehydrogenase activity
- identical protein binding
- protein binding
- flavin adenine dinucleotide binding
- butyryl-CoA dehydrogenase activity