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Deafness_IsolatedAndComplex v0.87 MIR96 Zornitza Stark Marked gene: MIR96 as ready
Deafness_IsolatedAndComplex v0.87 MIR96 Zornitza Stark Gene: mir96 has been classified as Amber List (Moderate Evidence).
Deafness_IsolatedAndComplex v0.87 MIR96 Zornitza Stark Phenotypes for gene: MIR96 were changed from Autosomal dominant hearing loss to Deafness, autosomal dominant 50, MIM# 613074
Deafness_IsolatedAndComplex v0.86 MIR96 Zornitza Stark Marked gene: MIR96 as ready
Deafness_IsolatedAndComplex v0.86 MIR96 Zornitza Stark Gene: mir96 has been classified as Amber List (Moderate Evidence).
Deafness_IsolatedAndComplex v0.86 MIR96 Zornitza Stark Phenotypes for gene: MIR96 were changed from to Autosomal dominant hearing loss
Deafness_IsolatedAndComplex v0.85 MIR96 Zornitza Stark Publications for gene: MIR96 were set to
Deafness_IsolatedAndComplex v0.85 MIR96 Zornitza Stark Mode of inheritance for gene: MIR96 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Deafness_IsolatedAndComplex v0.84 MIR96 Zornitza Stark Classified gene: MIR96 as Amber List (moderate evidence)
Deafness_IsolatedAndComplex v0.84 MIR96 Zornitza Stark Gene: mir96 has been classified as Amber List (Moderate Evidence).
Deafness_IsolatedAndComplex v0.81 MIR96 Lilian Downie reviewed gene: MIR96: Rating: AMBER; Mode of pathogenicity: None; Publications: 19363479, 29325119; Phenotypes: Autosomal dominant hearing loss; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Deafness_IsolatedAndComplex v0.0 MIR96 Zornitza Stark gene: MIR96 was added
gene: MIR96 was added to Deafness_MelbourneGenomics_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services,Melbourne Genomics Health Alliance Deafness Flagship
Mode of inheritance for gene: MIR96 was set to Unknown