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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 |
|---|---|---|---|
| 31 | ACACA | acetyl-CoA carboxylase alpha | |
| 51 | ACOX1 | acyl-CoA oxidase 1 | |
| 217 | ALDH2 | aldehyde dehydrogenase 2 family member | |
| 353 | APRT | adenine phosphoribosyltransferase | |
| 410 | ARSA | arylsulfatase A | |
| 1376 | CPT2 | carnitine palmitoyltransferase 2 | |
| 1431 | CS | citrate synthase | |
| 1890 | TYMP | thymidine phosphorylase | |
| 1892 | ECHS1 | enoyl-CoA hydratase, short chain 1 | |
| 2350 | FOLR2 | folate receptor beta |
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 |
