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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 |
|---|---|---|
| lipid homeostasis |
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:0000006 | Autosomal dominant inheritance |
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000248 | Brachycephaly |
| HP:0000286 | Epicanthus |
| HP:0000316 | Hypertelorism |
| HP:0000369 | Low-set ears |
| HP:0000407 | Sensorineural hearing impairment |
| HP:0000431 | Wide nasal bridge |
| HP:0000486 | Strabismus |
| HP:0000510 | Rod-cone dystrophy |
| 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 |
|---|---|---|---|
| 100135467 | CAVPO24639 | ||
| 101564686 | OCTDE08010 | ||
| 101705097 | HETGA13724 | ||
| 102463291 | PELSI11726 | ||
| 100562736 | ANOCA03050 | ||
| 103665753 | URSMA11004 | ||
| 114050814 | VOMUR12490 | ||
| 113877957 | BOBOX14597 | ||
| 102536864 | VICPA09943 | ||
| 100943743 | OTOGA14765 |
