acyl-CoA dehydrogenase short chain
| GO Term | Evidence Code | PMID |
|---|---|---|
| fatty acid beta-oxidation |
|
|
| fatty acid beta-oxidation |
|
|
| fatty acid beta-oxidation using acyl-CoA dehydrogenase |
|
|
| fatty acid beta-oxidation using acyl-CoA dehydrogenase |
|
|
| fatty acid beta-oxidation using acyl-CoA dehydrogenase |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| nucleus |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrion |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| acyl-CoA dehydrogenase activity |
|
|
| acyl-CoA dehydrogenase activity |
|
|
| acyl-CoA dehydrogenase activity |
|
|
| acyl-CoA dehydrogenase activity |
|
|
| acyl-CoA dehydrogenase activity |
|
| Gene Ontology |
|---|
| flavin adenine dinucleotide binding |
| oxidoreductase activity, acting on the CH-CH group of donors |
| oxidoreductase activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | |
| DOID:1574 | alcohol use disorder |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000252 | Microcephaly |
| HP:0000544 | External ophthalmoplegia |
| HP:0000648 | Optic atrophy |
| HP:0000708 | Atypical behavior |
| HP:0000709 | Psychosis |
| HP:0000750 | Delayed speech and language development |
| HP:0001250 | Seizure |
| HP:0001251 | Ataxia |
| HP:0001252 | Hypotonia |
| Disease ID | Disease Name |
|---|---|
| OMIM:201470 |
|
| ORPHA:26792 |
|
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: April 6, 2026