Dabigatran Pathway, Pharmacokinetics/Pharmacodynamics
Pathway network for the Dabigatran Pathway, Pharmacokinetics/Pharmacodynamics SuperPath
Sources:
- PharmGKB
- WikiPathways
Pathways in the Dabigatran Pathway, Pharmacokinetics/Pharmacodynamics SuperPath
| # | Name | Source | Genes |
|---|---|---|---|
| 1 | Dabigatran Pathway, Pharmacokinetics/Pharmacodynamics | PharmGKB | |
| 2 | Heroin metabolism | WikiPathways | |
| 3 | Methylphenidate Pathway, Pharmacokinetics | PharmGKB |
Ordered by rank within the SuperPath, via the multiplicity of each gene in the constituent pathways
| # | Symbol | Description | Category | # Related Pathways |
|---|---|---|---|---|
| 1 | CES1 | Carboxylesterase 1 | Protein Coding | 3 |
| 2 | CES2 | Carboxylesterase 2 | Protein Coding | 2 |
| 3 | UGT2B7 | UDP Glucuronosyltransferase Family 2 Member B7 | Protein Coding | 1 |
| 4 | UGT2B15 | UDP Glucuronosyltransferase Family 2 Member B15 | Protein Coding | 1 |
| 5 | UGT1A9 | UDP Glucuronosyltransferase Family 1 Member A9 | Protein Coding | 1 |
| 6 | F2 | Coagulation Factor II, Thrombin | Protein Coding | 1 |
Disorders associated with Dabigatran Pathway, Pharmacokinetics/Pharmacodynamics SuperPath
according to GeneCards Suite gene sharing
| # | Disorder | Type | Genes | Score |
|---|---|---|---|---|
| 1 | Drug metabolism, altered, ces1-related | Enrichment | CES1 | 4.13 |
| 2 | Prothrombin deficiency, congenital | Enrichment | F2 | 3.35 |
| 3 | Pregnancy loss, recurrent 2 | Enrichment | F2 | 3.35 |
| 4 | Prothrombin deficiency | Enrichment | F2 | 3.35 |
| 5 | Cerebral sinovenous thrombosis | Enrichment | F2 | 2.88 |
| 6 | Thrombophilia due to thrombin defect | Enrichment | F2 | 2.51 |
| 7 | Crigler-najjar syndrome, type i | Enrichment | UGT1A9 | 2.35 |
| 8 | Hyperbilirubinemia, transient familial neonatal | Enrichment | UGT1A9 | 2.35 |
| 9 | Stroke, ischemic | Enrichment | F2 | 2.35 |
| 10 | Bilirubin, serum level of, quantitative trait locus 1 | Enrichment | UGT1A9 | 2.35 |
| 11 | Crigler-najjar syndrome, type ii | Enrichment | UGT1A9 | 2.35 |
| 12 | Gilbert syndrome | Enrichment | UGT1A9 | 2.31 |
| 13 | Bilirubin metabolic disorder | Enrichment | UGT1A9 | 2.31 |
| 14 | Cerebral palsy | Enrichment | F2 | 1.77 |