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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 |
|---|---|---|
| hydrogen peroxide biosynthetic process | ||
| fatty acid beta-oxidation using acyl-CoA oxidase | ||
| spermatogenesis | ||
| fatty acid catabolic process | ||
| lipid 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:0110480 | autosomal recessive nonsyndromic deafness 22 | |
| DOID:0110481 | autosomal recessive nonsyndromic deafness 23 | |
| DOID:0110482 | autosomal recessive nonsyndromic deafness 24 | |
| DOID:0110483 | autosomal recessive nonsyndromic deafness 25 | |
| DOID:0110484 | autosomal recessive nonsyndromic deafness 26 | |
| DOID:0110485 | autosomal recessive nonsyndromic deafness 27 | |
| DOID:0110486 | autosomal recessive nonsyndromic deafness 28 | |
| DOID:0110487 | autosomal recessive nonsyndromic deafness 29 | |
| DOID:0110488 | autosomal recessive nonsyndromic deafness 3 | |
| DOID:0110489 | autosomal recessive nonsyndromic deafness 30 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0001508 | Failure to thrive |
| HP:0001522 | Death in infancy |
| HP:0001939 | Abnormality of metabolism/homeostasis |
| HP:0002007 | Frontal bossing |
| HP:0002015 | Dysphagia |
| HP:0002093 | Respiratory insufficiency |
| HP:0002167 | Abnormality of speech or vocalization |
| HP:0002240 | Hepatomegaly |
| HP:0002312 | Clumsiness |
| HP:0002353 | EEG abnormality |
| 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 |
