| BioCyc:MOUSE_PWY-6061 |
bile acid biosynthesis, neutral pathway |
| Reactome:R-HSA-194068 |
Bile acid and bile salt metabolism |
| Reactome:R-HSA-193807 |
Synthesis of bile acids and bile salts via 27-hydroxycholesterol |
| Reactome:R-HSA-211859 |
Biological oxidations |
| Reactome:R-HSA-211994 |
Sterols are 12-hydroxylated by CYP8B1 |
| Reactome:R-MMU-1430728 |
Metabolism |
| Reactome:R-MMU-556833 |
Metabolism of lipids |
| Reactome:R-MMU-8957322 |
Metabolism of steroids |
| Reactome:R-MMU-193775 |
Synthesis of bile acids and bile salts via 24-hydroxycholesterol |
| Reactome:R-MMU-211859 |
Biological oxidations |
| Reactome:R-MMU-211994 |
Sterols are 12-hydroxylated by CYP8B1 |
| Reactome:R-HSA-556833 |
Metabolism of lipids |
| Reactome:R-HSA-193775 |
Synthesis of bile acids and bile salts via 24-hydroxycholesterol |
| Reactome:R-HSA-211976 |
Endogenous sterols |
| Reactome:R-MMU-193368 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-MMU-211976 |
Endogenous sterols |
| Reactome:R-HSA-192105 |
Synthesis of bile acids and bile salts |
| Reactome:R-HSA-211945 |
Phase I - Functionalization of compounds |
| Reactome:R-MMU-194068 |
Bile acid and bile salt metabolism |
| Reactome:R-MMU-193807 |
Synthesis of bile acids and bile salts via 27-hydroxycholesterol |
| Reactome:R-MMU-211945 |
Phase I - Functionalization of compounds |
| Reactome:R-HSA-1430728 |
Metabolism |
| Reactome:R-HSA-8957322 |
Metabolism of steroids |
| Reactome:R-HSA-193368 |
Synthesis of bile acids and bile salts via 7alpha-hydroxycholesterol |
| Reactome:R-HSA-211897 |
Cytochrome P450 - arranged by substrate type |
| Reactome:R-MMU-192105 |
Synthesis of bile acids and bile salts |
| Reactome:R-MMU-211897 |
Cytochrome P450 - arranged by substrate type |
| PathBank:SMP0120468 |
Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0000318 |
Congenital Bile Acid Synthesis Defect Type III |
| PathBank:SMP0120463 |
Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0120467 |
Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0120495 |
Zellweger Syndrome |
| PathBank:SMP0000035 |
Bile Acid Biosynthesis |
| PathBank:SMP0000314 |
Congenital Bile Acid Synthesis Defect Type II |
| PathBank:SMP0000315 |
Cerebrotendinous Xanthomatosis (CTX) |
| PathBank:SMP0120652 |
27-Hydroxylase Deficiency |
| PathBank:SMP0120477 |
Familial Hypercholanemia (FHCA) |
| PathBank:SMP0000317 |
Familial Hypercholanemia (FHCA) |
| PathBank:SMP0000316 |
Zellweger Syndrome |
| PathBank:SMP0000720 |
27-Hydroxylase Deficiency |
| PathBank:SMP0063601 |
Bile Acid Biosynthesis |