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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Peroxisomal acyl-coenzyme A oxidase 1
Summary
- UniProt ID
- Q15067
- Gene Symbol
-
- ACOX1
- ACOX
- Organism
- Homo sapiens (human)
External Links
- GlyGen
- Q15067
- PubChem
- Q15067
- SwissLipids
- The Human Metabolome Database
- HMDBP00146
- The O-GlcNAc Database
- Q15067
- O-GlcNAcAtlas
- Q15067
Annotation
- Keyword
-
- Acetylation
- Alternative splicing
- Deafness
- Disease variant
- FAD
- Fatty acid metabolism
- Neuropathy
- Oxidoreductase
- Peroxisome
- Phosphoprotein
- Reference proteome
- Gene Ontology (GO)
| GO Term |
|---|
| peroxisome |
| cytosol |
| peroxisomal membrane |
| peroxisomal matrix |
| membrane |
Sequence
MNPDLRRERDSASFNPELLTHILDGSPEKTRRRREIENMILNDPDFQHEDLNFLTRSQRYEVAVRKSAIMVKKMREFGIADPDEIMWFKKLHLVNFVEPVGLNYSMFIPTLLNQGTTAQKEKWLLSSKGLQIIGTYAQTEMGHGTHLRGLETTATYDPETQEFILNSPTVTSIKWWPGGLGKTSNHAIVLAQLITKGKCYGLHAFIVPIREIGTHKPLPGITVGDIGPKFGYDEIDNGYLKMDNHRIPRENMLMKYAQVKPDGTYVKPLSNKLTYGTMVFVRSFLVGEAARALSKACTIAIRYSAVRHQSEIKPGEPEPQILDFQTQQYKLFPLLATAYAFQFVGAYMKETYHRINEGIGQGDLSELPELHALTAGLKAFTSWTANTGIEACRMACGGHGYSHCSGLPNIYVNFTPSCTFEGENTVMMLQTARFLMKSYDQVHSGKLVCGMVSYLNDLPSQRIQPQQVAVWPTMVDINSPESLTEAYKLRAARLVEIAAKNLQKEVIHRKSKEVAWNLTSVDLVRASEAHCHYVVVKLFSEKLLKIQDKAIQAVLRSLCLLYSLYGISQNAGDFLQGSIMTEPQITQVNQRVKELLTLIRSDAVALVDAFDFQDVTLGSVLGRYDGNVYENLFEWAKNSPLNKAEVHESYKHLKSLQSKL
Glycosylation Sites
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 20 |
|
G49108TO
Feature
: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt
Pathway
| Pathway Name | Organism |
|---|---|
| Peroxisomal protein import | Homo sapiens |
| TYSND1 cleaves peroxisomal proteins | Homo sapiens |
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
Disease
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:906 | peroxisomal disease | |
| DOID:92 | speech disorder | |
| DOID:9256 | colorectal cancer | |
| DOID:9273 | citrullinemia | |
| DOID:9306 | mechanical strabismus | |
| DOID:9452 | steatotic liver disease | |
| DOID:9649 | congenital nystagmus | |
| DOID:9650 | pathologic nystagmus | |
| DOID:9837 | hypertropia |
