Previous symbols: ASBT, ISBT. Aliases: NTCP2, IBAT.
Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.
| Disorder | Relationship | Where the gene appears |
|---|---|---|
| Primary Bile Acid Malabsorption | causative |
mechanism: Loss of ASBT Bile Acid Transport Function
|
| Progressive Familial Intrahepatic Cholestasis | no genetic record |
mechanism: Enterohepatic Bile Acid Recirculation
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.