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Susceptibility to Viral Infections v2.0 NFATC2 Gene migrated from ENSG00000101096 to ENSG00000101096 (gene set migration)
Susceptibility to Viral Infections v0.131 NFATC2 Bryony Thompson Publications for gene: NFATC2 were set to PMID: 38427060
Susceptibility to Viral Infections v0.130 NFATC2 Bryony Thompson Classified gene: NFATC2 as Amber List (moderate evidence)
Susceptibility to Viral Infections v0.130 NFATC2 Bryony Thompson Gene: nfatc2 has been classified as Amber List (Moderate Evidence).
Susceptibility to Viral Infections v0.129 NFATC2 Bryony Thompson reviewed gene: NFATC2: Rating: AMBER; Mode of pathogenicity: None; Publications: 35789258, 38427060; Phenotypes: Lymphoproliferative syndrome, MONDO:0016537, NFATC2-related; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Susceptibility to Viral Infections v0.122 NFATC2 Zornitza Stark Marked gene: NFATC2 as ready
Susceptibility to Viral Infections v0.122 NFATC2 Zornitza Stark Gene: nfatc2 has been classified as Red List (Low Evidence).
Susceptibility to Viral Infections v0.122 NFATC2 Zornitza Stark Phenotypes for gene: NFATC2 were changed from EBV associated lymphoproliferative disease to Lymphoproliferative syndrome, MONDO:0016537, NFATC2-related
Susceptibility to Viral Infections v0.121 NFATC2 Zornitza Stark Classified gene: NFATC2 as Red List (low evidence)
Susceptibility to Viral Infections v0.121 NFATC2 Zornitza Stark Gene: nfatc2 has been classified as Red List (Low Evidence).
Susceptibility to Viral Infections v0.120 NFATC2 Zornitza Stark reviewed gene: NFATC2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Lymphoproliferative syndrome, MONDO:0016537, NFATC2-related; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Susceptibility to Viral Infections v0.117 NFATC2 Peter McNaughton gene: NFATC2 was added
gene: NFATC2 was added to Susceptibility to Viral Infections. Sources: Literature
Mode of inheritance for gene: NFATC2 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: NFATC2 were set to PMID: 38427060
Phenotypes for gene: NFATC2 were set to EBV associated lymphoproliferative disease
Review for gene: NFATC2 was set to RED
Added comment: 12yo girl born to consanguineous parents with EBV associated lymphoproliferation. Initially presented with recurrent chest infections, lung deterioration, chronic wet cough and failure to thrive at the age of 9 and severe hypogammaglobulinaemia. Her elder brother died of lymphoma when he was 5 years old, otherwise family history was unremarkable.
Sources: Literature