Mitochondrial RNA degradation
Pathways in the Mitochondrial RNA degradation SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | Mitochondrial RNA degradation | Reactome | |
| 2 | FASTK family proteins regulate processing and stability of mitochondrial RNAs | Reactome |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | FASTK | Fas Activated Serine/Threonine Kinase | Protein Coding | 2 |
| 2 | FASTKD2 | FAST Kinase Domains 2 | Protein Coding | 2 |
| 3 | FASTKD5 | FAST Kinase Domains 5 | Protein Coding | 2 |
| 4 | TBRG4 | Transforming Growth Factor Beta Regulator 4 | Protein Coding | 2 |
| 5 | LRPPRC | Leucine Rich Pentatricopeptide Repeat Containing | Protein Coding | 1 |
| 6 | REXO2 | RNA Exonuclease 2 | Protein Coding | 1 |
| 7 | GRSF1 | G-Rich RNA Sequence Binding Factor 1 | Protein Coding | 1 |
| 8 | SUPV3L1 | Suv3 Like RNA Helicase | Protein Coding | 1 |
| 9 | SLIRP | SRA Stem-Loop Interacting RNA Binding Protein | Protein Coding | 1 |
| 10 | PNPT1 | Polyribonucleotide Nucleotidyltransferase 1 | Protein Coding | 1 |
Disorders associated with Mitochondrial RNA degradation SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Leigh syndrome, nuclear | Enrichment | FASTKD2, FASTKD5 | 3.82 |
| 2 | Leigh disease | Enrichment | FASTKD2, FASTKD5 | 3.73 |
| 3 | Fastkd2-related infantile mitochondrial encephalomyopathy | Enrichment | FASTKD2 | 3.53 |
| 4 | Combined oxidative phosphorylation deficiency 44 | Enrichment | FASTKD2 | 3.23 |
| 5 | Spinocerebellar ataxia 25 | Enrichment | PNPT1 | 3.13 |
| 6 | Combined oxidative phosphorylation deficiency 13 | Enrichment | PNPT1 | 3.13 |
| 7 | Deafness, autosomal recessive 70, with or without adult-onset neurodegeneration | Enrichment | PNPT1 | 2.83 |
| 8 | Autosomal recessive nonsyndromic deafness 70 | Enrichment | PNPT1 | 2.83 |
| 9 | Mitochondrial complex iv deficiency, nuclear type 5 | Enrichment | LRPPRC | 2.66 |
| 10 | Mitochondrial complex iv deficiency, nuclear type 1 | Enrichment | FASTKD2 | 2.19 |
| 11 | Mitochondrial encephalomyopathy | Enrichment | SLIRP | 2.13 |
| 12 | Rare autosomal recessive non-syndromic sensorineural deafness type dfnb | Enrichment | PNPT1 | 1.20 |