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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
mitochondrial metabolism disease
Summary
- Definition
- An inherited metabolic disorder that involves mitochondrial metabolism dysfunction.
- Super Class
- inherited metabolic disorder
Related Genes
| Gene ID | Gene Symbol | Description | Source |
|---|---|---|---|
| 2548 | GAA | alpha glucosidase | |
| 2632 | GBE1 | 1,4-alpha-glucan branching enzyme 1 | |
| 2678 | GGT1 | gamma-glutamyltransferase 1 | |
| 2876 | GPX1 | glutathione peroxidase 1 | |
| 3032 | HADHB | hydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | |
| 3155 | HMGCL | 3-hydroxy-3-methylglutaryl-CoA lyase | |
| 4594 | MMUT | methylmalonyl-CoA mutase | |
| 4968 | OGG1 | 8-oxoguanine DNA glycosylase | |
| 5160 | PDHA1 | pyruvate dehydrogenase E1 subunit alpha 1 | |
| 6389 | SDHA | succinate dehydrogenase complex flavoprotein subunit A |
Related Glycoprotein
| UniProt ID | Protein Name | Source |
|---|---|---|
| Q13085 | Acetyl-CoA carboxylase 1 | |
| Q15067 | Peroxisomal acyl-coenzyme A oxidase 1 | |
| Q6ZMG9 | Ceramide synthase 6 | |
| Q9C0K1 | Metal cation symporter ZIP8 | |
| Q9P212 | 1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1 |
