tRNA-uridine 2-thiolation (mammalian mitochondria)
Pathways in the tRNA-uridine 2-thiolation (mammalian mitochondria) SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | tRNA-uridine 2-thiolation (mammalian mitochondria) | PubChem |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
Disorders associated with tRNA-uridine 2-thiolation (mammalian mitochondria) SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Combined oxidative phosphorylation deficiency 10 | Enrichment | MTO1 | 3.53 |
| 2 | Combined oxidative phosphorylation deficiency 52 | Enrichment | NFS1 | 3.53 |
| 3 | Deafness, aminoglycoside-induced | Enrichment | TRMU | 3.53 |
| 4 | Combined oxidative phosphorylation deficiency 19 | Enrichment | NFS1 | 3.05 |
| 5 | Liver failure, infantile, transient | Enrichment | TRMU | 2.83 |
| 6 | Mitochondrial oxidative phosphorylation disorder | Enrichment | MTO1 | 2.83 |
| 7 | Mitochondrial myopathy with reversible cytochrome c oxidase deficiency | Enrichment | TRMU | 2.53 |
| 8 | Rare mitochondrial non-syndromic sensorineural deafness | Enrichment | TRMU | 2.53 |
