thyroid hormone metabolism II (via conjugation and/or degradation)
No Pathway Network information available for thyroid hormone metabolism II (via conjugation and/or degradation)
Pathways in the thyroid hormone metabolism II (via conjugation and/or degradation) SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | thyroid hormone metabolism II (via conjugation and/or degradation) | PubChem |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | UGT1A8 | UDP Glucuronosyltransferase Family 1 Member A8 | Protein Coding | 1 |
| 2 | SULT1A2 | Sulfotransferase Family 1A Member 2 | Protein Coding | 1 |
| 3 | DIO2 | Iodothyronine Deiodinase 2 | Protein Coding | 1 |
| 4 | SULT1A1 | Sulfotransferase Family 1A Member 1 | Protein Coding | 1 |
| 5 | UGT1A3 | UDP Glucuronosyltransferase Family 1 Member A3 | Protein Coding | 1 |
Disorders associated with thyroid hormone metabolism II (via conjugation and/or degradation) SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Crigler-najjar syndrome, type i | Enrichment | UGT1A3, UGT1A8 | 5.31 |
| 2 | Hyperbilirubinemia, transient familial neonatal | Enrichment | UGT1A3, UGT1A8 | 5.31 |
| 3 | Bilirubin, serum level of, quantitative trait locus 1 | Enrichment | UGT1A3, UGT1A8 | 5.31 |
| 4 | Crigler-najjar syndrome, type ii | Enrichment | UGT1A3, UGT1A8 | 5.31 |
| 5 | Gilbert syndrome | Enrichment | UGT1A3, UGT1A8 | 5.22 |
| 6 | Bilirubin metabolic disorder | Enrichment | UGT1A3, UGT1A8 | 5.22 |
