selenocysteine biosynthesis
Pathways in the selenocysteine biosynthesis SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | selenocysteine biosynthesis | PubChem |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | SEPHS1 | Selenophosphate Synthetase 1 | Protein Coding | 1 |
| 2 | SARS2 | Seryl-TRNA Synthetase 2, Mitochondrial | Protein Coding | 1 |
| 3 | SEPSECS | Sep (O-Phosphoserine) TRNA:Sec (Selenocysteine) TRNA Synthase | Protein Coding | 1 |
| 4 | PSTK | Phosphoseryl-TRNA Kinase | Protein Coding | 1 |
| 5 | SARS1 | Seryl-TRNA Synthetase 1 | Protein Coding | 1 |
| 6 | SEPHS2 | Selenophosphate Synthetase 2 | Protein Coding | 1 |
Disorders associated with selenocysteine biosynthesis SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Neurodevelopmental disorder with microcephaly, ataxia, and seizures | Enrichment | SARS1 | 3.35 |
| 2 | Hyperuricemia, pulmonary hypertension, renal failure, and alkalosis syndrome | Enrichment | SARS2 | 3.35 |
| 3 | Ververi-brady syndrome 2 | Enrichment | SEPHS1 | 3.35 |
| 4 | Kyphosis | Enrichment | SEPSECS | 2.88 |
| 5 | Pontocerebellar hypoplasia, type 2d | Enrichment | SEPSECS | 2.66 |
| 6 | Spastic diplegia | Enrichment | SEPSECS | 2.66 |
| 7 | Pontocerebellar hypoplasia, type 2e | Enrichment | SEPSECS | 2.51 |
| 8 | Pontocerebellar hypoplasia | Enrichment | SEPSECS | 2.10 |
| 9 | Arteriovenous malformations of the brain | Enrichment | SARS1 | 2.08 |
| 10 | Primary autosomal recessive microcephaly | Enrichment | SARS1 | 1.85 |
| 11 | Distal arthrogryposis | Enrichment | SEPSECS | 1.73 |
| 12 | Spastic ataxia | Enrichment | SEPSECS | 1.63 |
| 13 | Autosomal recessive non-syndromic intellectual disability | Enrichment | SARS1 | 1.60 |