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MIRAGE
acyl-CoA dehydrogenase family member 9
Summary
- Gene Symbol
-
- ACAD9
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- 3D-structure
- Acetylation
- Disease variant
- FAD
- Mitochondrion inner membrane
- Oxidoreductase
- Phosphoprotein
- Primary mitochondrial disease
- Proteomics identification
- Reference proteome
- Transit peptide
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| long-chain fatty acid metabolic process | ||
| mitochondrial respiratory chain complex I assembly | ||
| mitochondrial respiratory chain complex I assembly | ||
| medium-chain fatty acid metabolic process |
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus | ||
| mitochondrion | ||
| mitochondrion | ||
| mitochondrial inner membrane | ||
| mitochondrial inner membrane |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| acyl-CoA dehydrogenase activity | ||
| long-chain-acyl-CoA dehydrogenase activity | ||
| protein binding | ||
| flavin adenine dinucleotide binding | ||
| medium-chain-acyl-CoA dehydrogenase activity |
GO Hierarchy
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0112072 | nuclear type mitochondrial complex I deficiency 20 |
