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Mendelian susceptibility to Immune Disorders v0.22 IFNGR2 Zornitza Stark Marked gene: IFNGR2 as ready
Mendelian susceptibility to Immune Disorders v0.22 IFNGR2 Zornitza Stark Gene: ifngr2 has been classified as Green List (High Evidence).
Mendelian susceptibility to Immune Disorders v0.22 IFNGR2 Zornitza Stark Phenotypes for gene: IFNGR2 were changed from to Immunodeficiency 28, mycobacteriosis, MIM# 614889
Mendelian susceptibility to Immune Disorders v0.21 IFNGR2 Zornitza Stark Publications for gene: IFNGR2 were set to
Mendelian susceptibility to Immune Disorders v0.20 IFNGR2 Zornitza Stark Mode of inheritance for gene: IFNGR2 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Mendelian susceptibility to Immune Disorders v0.19 IFNGR2 Zornitza Stark reviewed gene: IFNGR2: Rating: GREEN; Mode of pathogenicity: None; Publications: 15924140, 18625743, 31222290; Phenotypes: Immunodeficiency 28, mycobacteriosis, MIM# 614889; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendelian susceptibility to Immune Disorders v0.19 IFNGR1 Zornitza Stark Marked gene: IFNGR1 as ready
Mendelian susceptibility to Immune Disorders v0.19 IFNGR1 Zornitza Stark Gene: ifngr1 has been classified as Green List (High Evidence).
Mendelian susceptibility to Immune Disorders v0.19 IFNGR1 Zornitza Stark Phenotypes for gene: IFNGR1 were changed from to Immunodeficiency 27A, mycobacteriosis, AR, MIM# 209950; Immunodeficiency 27B, mycobacteriosis, AD, MIM# 615978
Mendelian susceptibility to Immune Disorders v0.18 IFNGR1 Zornitza Stark Publications for gene: IFNGR1 were set to
Mendelian susceptibility to Immune Disorders v0.17 IFNGR1 Zornitza Stark Mode of inheritance for gene: IFNGR1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendelian susceptibility to Immune Disorders v0.16 IFNGR1 Zornitza Stark reviewed gene: IFNGR1: Rating: GREEN; Mode of pathogenicity: None; Publications: 7815885, 8960475, 9389728, 10811850, 10192386, 12244188, 15589309; Phenotypes: Immunodeficiency 27A, mycobacteriosis, AR, MIM# 209950, Immunodeficiency 27B, mycobacteriosis, AD, MIM# 615978; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Mendelian susceptibility to Immune Disorders v0.6 IFNG Zornitza Stark Phenotypes for gene: IFNG were changed from Mendelian susceptibility to mycobacterial disease to Mendelian susceptibility to mycobacterial disease; Immunodeficiency 69, MIM#618963
Mendelian susceptibility to Immune Disorders v0.5 IFNG Zornitza Stark edited their review of gene: IFNG: Changed phenotypes: Mendelian susceptibility to mycobacterial disease, Immunodeficiency 69, MIM#618963
Mendelian susceptibility to Immune Disorders v0.5 IFNG Zornitza Stark Marked gene: IFNG as ready
Mendelian susceptibility to Immune Disorders v0.5 IFNG Zornitza Stark Gene: ifng has been classified as Red List (Low Evidence).
Mendelian susceptibility to Immune Disorders v0.5 IFNG Zornitza Stark gene: IFNG was added
gene: IFNG was added to Mendelian susceptibility to Immune Disorders. Sources: Literature
Mode of inheritance for gene: IFNG was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: IFNG were set to 32163377
Phenotypes for gene: IFNG were set to Mendelian susceptibility to mycobacterial disease
Review for gene: IFNG was set to RED
Added comment: Two cousins with MSMD and homozygous intragenic deletion, some functional data.
Sources: Literature
Mendelian susceptibility to Immune Disorders v0.0 IFNGR2 Zornitza Stark gene: IFNGR2 was added
gene: IFNGR2 was added to Mendelian susceptibility to Immune Disorders_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship
Mode of inheritance for gene: IFNGR2 was set to Unknown
Mendelian susceptibility to Immune Disorders v0.0 IFNGR1 Zornitza Stark gene: IFNGR1 was added
gene: IFNGR1 was added to Mendelian susceptibility to Immune Disorders_MelbourneGenomics_AustralianGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Immunology Flagship
Mode of inheritance for gene: IFNGR1 was set to Unknown