acyl-CoA dehydrogenase medium chain
| UniProt | Protein Name |
|---|---|
| Q5T4U5 |
|
| P11310 |
|
| B7Z9I1 |
|
| A0A0S2Z366 |
|
| B4DJE7 |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| liver development |
|
|
| glycogen biosynthetic process |
|
|
| regulation of gluconeogenesis |
|
|
| fatty acid metabolic process |
|
|
| fatty acid beta-oxidation |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| mitochondrion |
|
|
| mitochondrion |
|
|
| mitochondrial matrix |
|
|
| mitochondrial matrix |
|
|
| mitochondrial matrix |
|
| GO Term | Evidence Code | PMID |
|---|---|---|
| acyl-CoA dehydrogenase activity |
|
|
| acyl-CoA dehydrogenase activity |
|
|
| acyl-CoA dehydrogenase activity |
|
|
| oxidoreductase activity, acting on the CH-CH group of donors |
|
|
| identical protein binding |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency |
| HPO ID | HPO Term |
|---|---|
| HP:0000007 | Autosomal recessive inheritance |
| HP:0000256 | Macrocephaly |
| HP:0000750 | Delayed speech and language development |
| HP:0001250 | Seizure |
| HP:0001251 | Ataxia |
| HP:0001252 | Hypotonia |
| HP:0001254 | Lethargy |
| HP:0001259 | Coma |
| HP:0001263 | Global developmental delay |
| HP:0001290 | Generalized hypotonia |
| Disease ID | Disease Name |
|---|---|
| OMIM:201450 |
|
| ORPHA:42 |
|
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