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Deafness_IsolatedAndComplex v0.514 MYO6 Zornitza Stark Marked gene: MYO6 as ready
Deafness_IsolatedAndComplex v0.514 MYO6 Zornitza Stark Gene: myo6 has been classified as Green List (High Evidence).
Deafness_IsolatedAndComplex v0.514 MYO6 Zornitza Stark Phenotypes for gene: MYO6 were changed from to Deafness, autosomal dominant 22, MIM# 606346; Deafness, autosomal recessive 37, MIM# 607821
Deafness_IsolatedAndComplex v0.513 MYO6 Zornitza Stark Publications for gene: MYO6 were set to
Deafness_IsolatedAndComplex v0.512 MYO6 Zornitza Stark Mode of inheritance for gene: MYO6 was changed from Unknown to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.511 MYO6 Zornitza Stark reviewed gene: MYO6: Rating: GREEN; Mode of pathogenicity: None; Publications: 24105371, 11468689, 25999546, 25227905, 18348273, 27171474; Phenotypes: Deafness, autosomal dominant 22, MIM# 606346, Deafness, autosomal recessive 37, MIM# 607821; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.0 MYO6 Zornitza Stark gene: MYO6 was added
gene: MYO6 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: MYO6 was set to Unknown