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Angelman Rett like syndromes v2.0 UBTF Gene migrated from ENSG00000108312 to ENSG00000108312 (gene set migration)
Angelman Rett like syndromes v0.90 UBTF Zornitza Stark Marked gene: UBTF as ready
Angelman Rett like syndromes v0.90 UBTF Zornitza Stark Gene: ubtf has been classified as Amber List (Moderate Evidence).
Angelman Rett like syndromes v0.90 UBTF Zornitza Stark Phenotypes for gene: UBTF were changed from to Neurodegeneration, childhood-onset, with brain atrophy, MIM# 617672; MONDO:0044701
Angelman Rett like syndromes v0.89 UBTF Zornitza Stark Publications for gene: UBTF were set to
Angelman Rett like syndromes v0.88 UBTF Zornitza Stark Mode of inheritance for gene: UBTF was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Angelman Rett like syndromes v0.87 UBTF Zornitza Stark Classified gene: UBTF as Amber List (moderate evidence)
Angelman Rett like syndromes v0.87 UBTF Zornitza Stark Gene: ubtf has been classified as Amber List (Moderate Evidence).
Angelman Rett like syndromes v0.86 UBTF Zornitza Stark reviewed gene: UBTF: Rating: AMBER; Mode of pathogenicity: None; Publications: 28777933, 29300972; Phenotypes: Neurodegeneration, childhood-onset, with brain atrophy, MIM# 617672, MONDO:0044701; Mode of inheritance: None
Angelman Rett like syndromes v0.0 UBTF Zornitza Stark gene: UBTF was added
gene: UBTF was added to Angelman Rett like syndromes_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: UBTF was set to Unknown