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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
acyl-CoA oxidase 1
Summary
- Gene Symbol
-
- ACOX1
- Aliases
-
- PALMCOX
- palmitoyl-CoA oxidase
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Acetylation
- Alternative splicing
- Deafness
- Disease variant
- FAD
- Fatty acid metabolism
- Neuropathy
- Oxidoreductase
- Peroxisome
- Phosphoprotein
- Reference proteome
- Proteins
| UniProt | Protein Name |
|---|---|
| Q15067 |
|
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| very long-chain fatty acid metabolic process | ||
| very long-chain fatty acid beta-oxidation | ||
| fatty acid oxidation | ||
| generation of precursor metabolites and energy | ||
| prostaglandin metabolic process |
GO Hierarchy
biological process
metabolic process [inference]
catabolic process [inference]
cellular metabolic process [inference]
primary metabolic process [inference]
small molecule metabolic process [inference]
organic substance metabolic process [inference]
cellular process [inference]
| GO Term | Evidence Code | PMID |
|---|---|---|
| cytosol |
|
|
| membrane | ||
| peroxisome | ||
| peroxisomal membrane | ||
| peroxisomal matrix |
|
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| flavin adenine dinucleotide binding | ||
| protein homodimerization activity | ||
| fatty acid binding | ||
| acyl-CoA oxidase activity | ||
| PDZ domain binding |
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Rhea
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0110570 | autosomal dominant nonsyndromic deafness 47 | |
| DOID:0110571 | autosomal dominant nonsyndromic deafness 48 | |
| DOID:0110572 | autosomal dominant nonsyndromic deafness 49 | |
| DOID:0110573 | autosomal dominant nonsyndromic deafness 4A | |
| DOID:0110574 | autosomal dominant nonsyndromic deafness 4B | |
| DOID:0110575 | autosomal dominant nonsyndromic deafness 5 | |
| DOID:0110576 | autosomal dominant nonsyndromic deafness 50 | |
| DOID:0110577 | autosomal dominant nonsyndromic deafness 51 | |
| DOID:0110578 | autosomal dominant nonsyndromic deafness 52 | |
| DOID:0110579 | autosomal dominant nonsyndromic deafness 53 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001250 | Seizure |
| HP:0001252 | Hypotonia |
| HP:0001263 | Global developmental delay |
| HP:0001276 | Hypertonia |
| HP:0001288 | Gait disturbance |
| HP:0001298 | Encephalopathy |
| HP:0001319 | Neonatal hypotonia |
| HP:0001332 | Dystonia |
| HP:0001344 | Absent speech |
| HP:0001347 | Hyperreflexia |
| Disease ID | Disease Name |
|---|---|
| ORPHA:2971 |
|
| OMIM:264470 |
|
| OMIM:618960 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
LIPID MAPS Gene / Proteome Database
- LMPD ID
- LMP002411
- Gene Name
- acyl-CoA oxidase 1, palmitoyl
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 173162 | WB:WBGene00008564 | ||
| 173163 | WB:WBGene00008565 | ||
| 173164 | WB:WBGene00008567 | ||
| 176353 | WB:WBGene00008167 | ||
| 181668 | WB:WBGene00010336 | ||
| 184167 | WB:WBGene00008566 | ||
| 31641 | FB:FBgn0029924 | ||
| 37028 | FB:FBgn0027572 | ||
| 37445 | FB:FBgn0034628 | ||
| 37446 | FB:FBgn0034629 |
