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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:0110540 | autosomal recessive nonsyndromic deafness 98 | |
| DOID:0110541 | autosomal dominant nonsyndromic deafness 1 | |
| DOID:0110542 | autosomal dominant nonsyndromic deafness 10 | |
| DOID:0110543 | autosomal dominant nonsyndromic deafness 11 | |
| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | |
| DOID:0110545 | autosomal dominant nonsyndromic deafness 13 | |
| DOID:0110546 | autosomal dominant nonsyndromic deafness 15 | |
| DOID:0110547 | autosomal dominant nonsyndromic deafness 16 | |
| DOID:0110548 | autosomal dominant nonsyndromic deafness 17 | |
| DOID:0110549 | autosomal dominant nonsyndromic deafness 18 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0002355 | Difficulty walking |
| HP:0002376 | Developmental regression |
| HP:0002415 | Leukodystrophy |
| HP:0002500 | Abnormal cerebral white matter morphology |
| HP:0002522 | Areflexia of lower limbs |
| HP:0002747 | Respiratory insufficiency due to muscle weakness |
| HP:0002910 | Elevated circulating hepatic transaminase concentration |
| HP:0003186 | Inverted nipples |
| HP:0003390 | Sensory axonal neuropathy |
| HP:0003487 | Babinski sign |
| 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 |
