Previous symbols: IFNGT1. Aliases: AF-1.
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 |
|---|---|---|
| Immunodeficiency 28 | causative germline loss of function |
mechanism: Failure of Hexameric IFN-gamma Receptor Assembly; IFNGR2 Loss-of-Function Variant
|
| Invasive Non-Typhoidal Salmonellosis | susceptibility | |
| Down_syndrome |
untyped
Risk Factor
|
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.