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Mendelian susceptibility to Immune Disorders v0.16 ZNFX1 Zornitza Stark Publications for gene: ZNFX1 were set to 33876776
Mendelian susceptibility to Immune Disorders v0.15 ZNFX1 Chirag Patel Classified gene: ZNFX1 as Green List (high evidence)
Mendelian susceptibility to Immune Disorders v0.15 ZNFX1 Chirag Patel Gene: znfx1 has been classified as Green List (High Evidence).
Mendelian susceptibility to Immune Disorders v0.14 ZNFX1 Chirag Patel reviewed gene: ZNFX1: Rating: GREEN; Mode of pathogenicity: None; Publications: PubMed: 33872655, 34708404; Phenotypes: Immunodeficiency 91 and hyperinflammation, MIM# 619644; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mendelian susceptibility to Immune Disorders v0.14 ZNFX1 Zornitza Stark Phenotypes for gene: ZNFX1 were changed from Susceptibility to mycobacterial infection to Immunodeficiency 91 and hyperinflammation, MIM# 619644
Mendelian susceptibility to Immune Disorders v0.13 ZNFX1 Zornitza Stark edited their review of gene: ZNFX1: Changed phenotypes: Immunodeficiency 91 and hyperinflammation, MIM# 619644
Mendelian susceptibility to Immune Disorders v0.10 ZNFX1 Zornitza Stark Marked gene: ZNFX1 as ready
Mendelian susceptibility to Immune Disorders v0.10 ZNFX1 Zornitza Stark Gene: znfx1 has been classified as Amber List (Moderate Evidence).
Mendelian susceptibility to Immune Disorders v0.10 ZNFX1 Zornitza Stark Classified gene: ZNFX1 as Amber List (moderate evidence)
Mendelian susceptibility to Immune Disorders v0.10 ZNFX1 Zornitza Stark Gene: znfx1 has been classified as Amber List (Moderate Evidence).
Mendelian susceptibility to Immune Disorders v0.9 ZNFX1 Zornitza Stark gene: ZNFX1 was added
gene: ZNFX1 was added to Mendelian susceptibility to Immune Disorders. Sources: Literature
Mode of inheritance for gene: ZNFX1 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: ZNFX1 were set to 33876776
Phenotypes for gene: ZNFX1 were set to Susceptibility to mycobacterial infection
Review for gene: ZNFX1 was set to AMBER
Added comment: Four indviduals from two unrelated kindreds reported with intermittent monocytosis and mycobacterial disease, including bacillus Calmette-Guérin-osis and disseminated tuberculosis.
Sources: Literature