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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
acyl-CoA oxidase
Summary
- Gene Symbol
-
- POX1
- Organism
- Saccharomyces cerevisiae S288C
Annotation
- Keyword
-
- FAD
- Fatty acid metabolism
- Oxidoreductase
- Peroxisome
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| P13711 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid metabolic process | ||
| fatty acid beta-oxidation using acyl-CoA oxidase | ||
| lipid homeostasis |
|
|
| fatty acid beta-oxidation |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| peroxisome | ||
| intracellular membrane-bounded organelle | ||
| peroxisomal matrix | ||
| cytoplasm |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| oxidoreductase activity | ||
| acyl-CoA oxidase activity | ||
| fatty acid binding | ||
| FAD binding | ||
| flavin adenine dinucleotide binding |
GO Hierarchy
OrthoDB (Group)
- Group level
- Eukaryota
- Group Name
- Acyl-CoA oxidase
- Functional Category
-
- I: Lipid transport and metabolism
- P: Inorganic ion transport and metabolism
- Q: Secondary metabolites biosynthesis, transport and catabolism
Alliance of Genome Resources
- Expression
| Location | References |
|---|---|
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0050797 | peroxisomal acyl-CoA oxidase deficiency | |
| DOID:0070516 | Mitchell syndrome | |
| DOID:0111067 | congenital bile acid synthesis defect 6 | |
| DOID:9452 | steatotic liver disease | |
| DOID:9970 | obesity |
Ortholog
| Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|---|
| 51 | HGNC:119 | |||
| 8309 | HGNC:120 | |||
| 11430 | MGI:1330812 | |||
| 33898 | FB:FBgn0031813 | |||
| 35213 | FB:FBgn0032775 | |||
| 50681 | RGD:619757 | |||
| 55289 | HGNC:25621 | |||
| 74121 | MGI:1921371 | |||
| 93732 | MGI:1934852 | |||
| 173162 | WB:WBGene00008564 |
