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Primary immunodeficiency

Gene: IFNGR1

Green List (high evidence)

IFNGR1 (interferon gamma receptor 1)
EnsemblGeneIds (GRCh38): ENSG00000027697
EnsemblGeneIds (GRCh37): ENSG00000027697
OMIM: 107470, Gene2Phenotype
IFNGR1 is in 3 panels

4 reviews

Kimberly Gilmour (Great Ormond Street Hopsital)

Green List (high evidence)

agree with green gene
Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94

Tracy Briggs (Manchester Genomic Medicine Centre)

Green List (high evidence)

YES- this is covered on our targeted exome
Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94

Sophie Hambleton (Newcastle University)

Green List (high evidence)

Mode of inheritance
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal

Louise Daugherty (Genomics England Curator)

Green List (high evidence)

Gene rating submitted by Kimberly Gilmour and Austen Worth on behalf of London North GLH for the GMS Immunology specialist test group. As discussed with the GMS Immunology Specialist Test Group during webex call 28th March 2019 and confirmed in follow up email 6th September the Specialist Test Group all agreed there is enough evidence to rate this gene Green.
Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
Gene rating submitted by Tracy Briggs, David Gokhale and Abigal Rousseau on behalf of North West GLH for the GMS Immunology specialist test group. As discussed with the GMS Immunology Specialist Test Group during webex call 28th March 2019 and confirmed in follow up email on 20th June the Specialist Test Group all agreed there is enough evidence to rate this gene Green.
Created: 17 Sep 2019, 3:18 p.m. | Last Modified: 17 Sep 2019, 3:18 p.m.
Panel Version: 1.94
OriginaI Metadata from IUIS classification table (February, 2018) downloaded 20180614. IUIS Genetic defect (original gene symbol in IUIS download): IFNGR1 .PanelApp HGNC gene symbol check: IFNGR1 . IUIS Disease: IFN-g receptor 1 deficiency . IUIS Inheritance: AR /AD .T cells: Normal to decreased, .B cells: N/A, .IUIS Other affected cells: M + L. IUIS Associated features: Susceptibility to mycobacteria and Salmonella. IUIS Major category: Defects in Intrinsic and Innate Immunity. IUIS Subcategory: Mendelian Susceptibility to mycobacterial disease (MSMD)
Created: 2 Jul 2018, 10:35 a.m.
Comment on list classification: Changed Amber to Green from external expert review and further publications to support gene-disease association
Created: 21 Jun 2018, 12:57 p.m.
Comment on publications: added publication to support gene-disease association
Created: 21 Jun 2018, 12:57 p.m.
Comment on phenotypes: added MOI to phenotypes and OMIM MIMid
Created: 21 Jun 2018, 12:55 p.m.
Comment on mode of inheritance: amended MOI from expert review, and reflected this in the phenotypes
Created: 21 Jun 2018, 12:54 p.m.
This gene was absent from the original PanelApp PID panel dataset (review April 2018). However it was listed in external expert immunodeficiency diagnostic gene list(s) GOSH or GRID. In this combined PID panel, this gene has been rated as AMBER and needs further curational review to assess pertinence prior to v1.
Created: 20 Apr 2018, 12:25 p.m.
Original metadata downloaded from ESID Registry. ESID_Gene_original: IFNGR1, PanelApp HGNC gene symbol check: IFNGR1, ESID classification: Main_category/ Sub_category/ PID_Diagnosis Phagocytic disorders / Defects with susceptibility to mycobacterial infection (MSMD) / Defects with susceptibility to mycobacterial infection (MSMD)
Created: 17 Apr 2018, 12:29 p.m.
Original metadata supplied by GRID. GRID Gene Symbol HGNC PanelApp check: IFNGR1, GRID_Gene_Symbol: IFNGR1, GRID_Transcript_ENS_Community submitted: ENST00000367739, GRID_Transcript_RefSeq: NM_000416.2, GRID_Transcript_ENS_used_on_Production: ENST00000367739
Created: 17 Apr 2018, 12:12 p.m.

Details

Mode of Inheritance
BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Sources
  • NHS GMS
  • North West GLH
  • London North GLH
  • IUIS Classification February 2018
  • Victorian Clinical Genetics Services
  • Expert Review Green
  • ESID Registry 20171117
  • GRID V2.0
Phenotypes
  • Immunodeficiency 27A, (AR) 209950
  • Immunodeficiency 27B, (AD) 615978
  • Mycobacteriosis
  • Defects with susceptibility to mycobacterial infection (MSMD)
  • Susceptibility to mycobacteria and Salmonella
  • Defects in Intrinsic and Innate Immunity
OMIM
107470
Clinvar variants
Variants in IFNGR1
Penetrance
None
Publications
Panels with this gene

History Filter Activity

17 Sep 2019, Gel status: 3

Added New Source

Louise Daugherty (Genomics England Curator)

Source NHS GMS was added to IFNGR1.

17 Sep 2019, Gel status: 3

Added New Source

Louise Daugherty (Genomics England Curator)

Source North West GLH was added to IFNGR1.

17 Sep 2019, Gel status: 3

Added New Source

Louise Daugherty (Genomics England Curator)

Source London North GLH was added to IFNGR1.

12 Jul 2018, Gel status: 4

Panel promoted to version 1.0

Louise Daugherty (Genomics England Curator)

2018-07-12 Louise Daugherty (Genomics England Curator) promoted panel to v1.0. Reviews were assessed, and panel was revised according to expert reviews and further in-house curation based on PanelApp guidelines. Previous panels (A- or hypo-gammaglobulinaemia, Congenital neutropaenia, Agranulocytosis, Combined B and T cell defect, Inherited complement deficiency and SCID panels) that were merged with this panel, were checked again for any changes/new reviews prior to versioning of this panel, these merged panels are now retired/made internal.

1 Jul 2018, Gel status: 4

Set penetrance

Louise Daugherty (Genomics England Curator)

Phenotypes for gene IFNGR1 were set to Immunodeficiency 27A, (AR) 209950, Immunodeficiency 27B, (AD) 615978, Mycobacteriosis, Defects with susceptibility to mycobacterial infection (MSMD), Susceptibility to mycobacteria and Salmonella, Defects in Intrinsic and Innate Immunity

26 Jun 2018, Gel status: 4

Added New Source

Louise Daugherty (Genomics England Curator)

IUIS Classification February 2018 was added to IFNGR1. Panel: Primary immunodeficiency disorders

26 Jun 2018, Gel status: 4

Added New Source

Louise Daugherty (Genomics England Curator)

Victorian Clinical Genetics Services was added to IFNGR1. Panel: Primary immunodeficiency disorders

21 Jun 2018, Gel status: 3

Entity classified by Genomics England curator

Louise Daugherty (Genomics England Curator)

Gene: ifngr1 has been classified as Green List (High Evidence).

21 Jun 2018, Gel status: 3

Entity classified by Genomics England curator

Louise Daugherty (Genomics England Curator)

Gene: ifngr1 has been classified as Green List (High Evidence).

21 Jun 2018, Gel status: 2

Set publications

Louise Daugherty (Genomics England Curator)

Publications for gene: IFNGR1 were set to 8960473; 8960475; 9389728; 9497247; 9497247

21 Jun 2018, Gel status: 2

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for gene: IFNGR1 were set to Immunodeficiency 27A, (AR) 209950; Immunodeficiency 27B, (AD) 615978; Mycobacteriosis; Defects with susceptibility to mycobacterial infection (MSMD)

21 Jun 2018, Gel status: 2

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for gene: IFNGR1 were set to Immunodeficiency 27A, (AR) 209950; Immunodeficiency 27B, (AD) 615978; Mycobacteriosis; Defects with susceptibility to mycobacterial infection (MSMD)

21 Jun 2018, Gel status: 2

Set mode of inheritance

Louise Daugherty (Genomics England Curator)

Mode of inheritance for gene: IFNGR1 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal

20 Apr 2018, Gel status: 2

Set Phenotypes

Louise Daugherty (Genomics England Curator)

Phenotypes for IFNGR1 were set to Immunodeficiency 27A; Immunodeficiency 27B; Mycobacteriosis; Defects with susceptibility to mycobacterial infection (MSMD)

20 Apr 2018, Gel status: 2

Added New Source

Louise Daugherty (Genomics England Curator)

Expert Review Amber was added to IFNGR1. Panel: Primary immunodeficiency disorders

17 Apr 2018, Gel status: 1

Added New Source, Set penetrance

Louise Daugherty (Genomics England Curator)

ESID Registry 20171117 was added to IFNGR1. Panel: Primary immunodeficiency disorders Phenotypes for gene IFNGR1 were set to Immunodeficiency 27A, Immunodeficiency 27B, Mycobacteriosis, Immunodeficiency 27B, Mycobacteriosis, Defects with susceptibility to mycobacterial infection (MSMD)

17 Apr 2018, Gel status: 1

Set penetrance

Louise Daugherty (Genomics England Curator)

Phenotypes for gene IFNGR1 were set to Immunodeficiency 27A, Immunodeficiency 27B, Mycobacteriosis, Immunodeficiency 27B, Mycobacteriosis

17 Apr 2018, Gel status: 1

Added New Source

Louise Daugherty (Genomics England Curator)

IFNGR1 was added to Primary immunodeficiency disorders panel. Sources: GRID V2.0

17 Apr 2018, Gel status: 1

Created

Louise Daugherty (Genomics England Curator)

IFNGR1 was created by Louise Daugherty