Mitochondrial fatty acid synthesis pathway
Pathways in the Mitochondrial fatty acid synthesis pathway SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | Mitochondrial fatty acid synthesis pathway | WikiPathways |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | OXSM | 3-Oxoacyl-ACP Synthase, Mitochondrial | Protein Coding | 1 |
| 2 | HSD17B12 | Hydroxysteroid 17-Beta Dehydrogenase 12 | Protein Coding | 1 |
| 3 | MCAT | Malonyl-CoA-Acyl Carrier Protein Transacylase | Protein Coding | 1 |
| 4 | HTD2 | Hydroxyacyl-Thioester Dehydratase Type 2 | Protein Coding | 1 |
| 5 | MECR | Mitochondrial Trans-2-Enoyl-CoA Reductase | Protein Coding | 1 |
| 6 | ACACA | Acetyl-CoA Carboxylase Alpha | Protein Coding | 1 |
Disorders associated with Mitochondrial fatty acid synthesis pathway SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Optic atrophy 15 | Enrichment | MCAT | 3.35 |
| 2 | Optic atrophy 16 | Enrichment | MECR | 3.35 |
| 3 | Acetyl-coa carboxylase-alpha deficiency | Enrichment | ACACA | 3.35 |
| 4 | Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities | Enrichment | MECR | 3.35 |
| 5 | Autosomal recessive isolated optic atrophy | Enrichment | MCAT | 2.75 |
| 6 | Optic atrophy plus syndrome | Enrichment | MECR | 1.71 |
| 7 | Mitochondrial disease | Enrichment | MECR | 1.42 |