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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: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 |
|---|---|---|---|
| 100186673 | CIOIN12803 | ||
| 103175663 | CALMI07688 | ||
| 102353101 | LATCH15530 | ||
| 449662 | ZFIN:ZDB-GENE-041010-219 | DANRE39282 | |
| 108273108 | ICTPU03243 | ||
| 113583258 | ELEEL31179 | ||
| 100380562 | SALSA19696 | ||
| 100380782 | SALSA19696 | ||
| 115178807 | SALTR67537 | ||
| 115208632 | SALTR38655 |
