Previous symbols: IFNGR. Aliases: CD119.
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 |
|---|---|---|
| Autosomal Dominant Mendelian Susceptibility To Mycobacterial Diseases Due To Partial IFNgammaR1 Deficiency | causative germline dominant negative |
mechanism: Dominant-Negative Impairment of IFN-gamma Signaling; Heterozygous IFNGR1 Exon 6 Frameshift Deletion; Heterozygous IFNGR1 Exon 6 Frameshift Insertion; Heterozygous IFNGR1 Exon 6 Nonsense Substitution
|
| Invasive Non-Typhoidal Salmonellosis | susceptibility |
Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.