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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:0110470 | autosomal recessive nonsyndromic deafness 15 | |
| DOID:0110471 | autosomal recessive nonsyndromic deafness 16 | |
| DOID:0110472 | autosomal recessive nonsyndromic deafness 17 | |
| DOID:0110473 | autosomal recessive nonsyndromic deafness 18A | |
| DOID:0110474 | autosomal recessive nonsyndromic deafness 18B | |
| DOID:0110475 | autosomal recessive nonsyndromic deafness 1A | |
| DOID:0110476 | autosomal recessive nonsyndromic deafness 1B | |
| DOID:0110477 | autosomal recessive nonsyndromic deafness 2 | |
| DOID:0110478 | autosomal recessive nonsyndromic deafness 20 | |
| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000512 | Abnormal electroretinogram |
| HP:0000545 | Myopia |
| HP:0000580 | Pigmentary retinopathy |
| HP:0000639 | Nystagmus |
| HP:0000648 | Optic atrophy |
| HP:0000649 | Abnormality of visual evoked potentials |
| HP:0000654 | Decreased light- and dark-adapted electroretinogram amplitude |
| HP:0000668 | Hypodontia |
| HP:0000737 | Irritability |
| HP:0001161 | Hand polydactyly |
| 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 |
