Previous symbols: OPG. Aliases: OCIF, TR1.
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 |
|---|---|---|
| Juvenile Paget Disease | causative germline loss of function |
mechanism: Biallelic TNFRSF11B Loss of Function
|
| Legg-Calve-Perthes Disease | risk factor |
mechanism: Resorption-Dominant Revascularization and Fragmentation of the Femoral Head
|
| Otosclerosis | unknown |
mechanism: Reduced Osteoprotegerin Restraint of Osteoclastogenesis
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.