plasmalogen biosynthesis
Pathways in the plasmalogen biosynthesis SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | plasmalogen biosynthesis | PubChem |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | ETNK1 | Ethanolamine Kinase 1 | Protein Coding | 1 |
| 2 | FAR1 | Fatty Acyl-CoA Reductase 1 | Protein Coding | 1 |
| 3 | AGPS | Alkylglycerone Phosphate Synthase | Protein Coding | 1 |
| 4 | SELENOI | Selenoprotein I | Protein Coding | 1 |
| 5 | GNPAT | Glyceronephosphate O-Acyltransferase | Protein Coding | 1 |
| 6 | PCYT1A | Phosphate Cytidylyltransferase 1A, Choline | Protein Coding | 1 |
| 7 | PCYT2 | Phosphate Cytidylyltransferase 2, Ethanolamine | Protein Coding | 1 |
| 8 | CHKA | Choline Kinase Alpha | Protein Coding | 1 |
| 9 | CEPT1 | Choline/Ethanolamine Phosphotransferase 1 | Protein Coding | 1 |
| 10 | AGPAT1 | 1-Acylglycerol-3-Phosphate O-Acyltransferase 1 | Protein Coding | 1 |
Disorders associated with plasmalogen biosynthesis SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Rhizomelic chondrodysplasia punctata | Enrichment | AGPS, GNPAT | 5.53 |
| 2 | Rhizomelic chondrodysplasia punctata, type 2 | Enrichment | GNPAT | 3.13 |
| 3 | Peroxisomal fatty acyl-coa reductase 1 disorder | Enrichment | FAR1 | 3.13 |
| 4 | Neurodevelopmental disorder with microcephaly, movement abnormalities, and seizures | Enrichment | CHKA | 3.13 |
| 5 | Rhizomelic chondrodysplasia punctata, type 3 | Enrichment | AGPS | 3.13 |
| 6 | Spastic paraplegia 81, autosomal recessive | Enrichment | SELENOI | 3.13 |
| 7 | Cataracts, spastic paraparesis, and speech delay | Enrichment | FAR1 | 3.13 |
| 8 | Fatty acyl-coa reductase 1 deficiency | Enrichment | FAR1 | 3.13 |
| 9 | Spondylometaphyseal dysplasia with cone-rod dystrophy | Enrichment | PCYT1A | 2.83 |
| 10 | Spastic paraplegia 82, autosomal recessive | Enrichment | PCYT2 | 2.83 |
| 11 | Lipodystrophy, congenital generalized, type 5 | Enrichment | PCYT1A | 2.83 |
| 12 | Autosomal recessive non-syndromic intellectual disability | Enrichment | CHKA | 1.38 |
| 13 | Leber plus disease | Enrichment | PCYT1A | 1.17 |
| 14 | Microcephaly | Enrichment | CHKA | 1.06 |