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Newborns main panel

Gene: IFNGR2

Green List (high evidence)
IFNGR2 (interferon gamma receptor 2)
EnsemblGeneIds (GRCh38): ENSG00000159128
EnsemblGeneIds (GRCh37): ENSG00000159128
OMIM: 147569, Gene2Phenotype
IFNGR2 is in 2 panels

1 review

Mafalda Gomes (Genomics England Curator)

The mechanism of pathogenicity is loss-of-function (LOF).
Created: 1 Jun 2023, 2:40 p.m. | Last Modified: 1 Jun 2023, 2:40 p.m.
Panel Version: 0.137
https://pubmed.ncbi.nlm.nih.gov/31497017/
Created: 1 Jun 2023, 12:22 p.m. | Last Modified: 1 Jun 2023, 12:22 p.m.
Panel Version: 0.134
Created: 1 Jun 2023, 12:22 p.m.
Last Modified: 1 Jun 2023, 12:22 p.m.
Panel version: 0.137

Details

Mode of Inheritance
BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • Immunodeficiency 28, mycobacteriosis
OMIM
147569
Clinvar variants
Variants in IFNGR2
Penetrance
None
Panels with this gene

History Filter Activity

14 Sep 2023, Gel status: 3

Set Phenotypes

Mafalda Gomes (Genomics England Curator)

Added phenotypes Immunodeficiency 28, mycobacteriosis for gene: IFNGR2

5 Jul 2023, Gel status: 3

Set Phenotypes

Mafalda Gomes (Genomics England Curator)

Added phenotypes Immunodeficiency 28, mycobacteriosis for gene: IFNGR2

15 May 2023, Gel status: 3

Added New Source, Set Phenotypes, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Green was added to IFNGR2. Added phenotypes Immunodeficiency 28, mycobacteriosis for gene: IFNGR2 Rating Changed from No List (delete) to Green List (high evidence)

5 May 2023, Gel status: 0

Added New Source, Status Update

Mafalda Gomes (Genomics England Curator)

Source Expert Review Removed was added to IFNGR2. Rating Changed from Green List (high evidence) to No List (delete)

9 Mar 2023, Gel status: 3

Created, Added New Source, Set mode of inheritance

Mafalda Gomes (Genomics England Curator)

gene: IFNGR2 was added gene: IFNGR2 was added to Newborns main panel. Sources: Expert Review Green Mode of inheritance for gene: IFNGR2 was set to BIALLELIC, autosomal or pseudoautosomal