Aliases: KIAA1119.
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 |
|---|---|---|
| Microvillus Inclusion Disease | causative germline | |
| Osteootohepatoenteric Syndrome | cooperating | |
| Progressive Familial Intrahepatic Cholestasis | causative germline |
mechanism: Apical Trafficking Failure of Canalicular Transporters; Canalicular Bile Formation Defect
subtype: MYO5B-related cholestasis
scoped to subtype: MYO5B-related cholestasis
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.