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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 |
|---|---|---|---|
| 6390 | SDHB | succinate dehydrogenase complex iron sulfur subunit B | |
| 6391 | SDHC | succinate dehydrogenase complex subunit C | |
| 6576 | SLC25A1 | solute carrier family 25 member 1 | |
| 6646 | SOAT1 | sterol O-acyltransferase 1 | |
| 6652 | SORD | sorbitol dehydrogenase | |
| 6783 | SULT1E1 | sulfotransferase family 1E member 1 | |
| 8630 | HSD17B6 | hydroxysteroid 17-beta dehydrogenase 6 | |
| 51196 | PLCE1 | phospholipase C epsilon 1 | |
| 55750 | AGK | acylglycerol kinase | |
| 64116 | SLC39A8 | solute carrier family 39 member 8 |
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 |
