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Deafness_IsolatedAndComplex v0.452 DFNB59 Zornitza Stark Marked gene: DFNB59 as ready
Deafness_IsolatedAndComplex v0.452 DFNB59 Zornitza Stark Gene: dfnb59 has been classified as Green List (High Evidence).
Deafness_IsolatedAndComplex v0.452 DFNB59 Zornitza Stark Phenotypes for gene: DFNB59 were changed from to Deafness, autosomal recessive 59, MIM# 610220
Deafness_IsolatedAndComplex v0.451 DFNB59 Zornitza Stark Publications for gene: DFNB59 were set to
Deafness_IsolatedAndComplex v0.450 DFNB59 Zornitza Stark Mode of inheritance for gene: DFNB59 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.449 DFNB59 Zornitza Stark changed review comment from: DEFINITIVE by ClinGen, over 50 affected individuals from more than 10 families reported, supportive functional data including animal models.; to: DEFINITIVE by ClinGen, over 50 affected individuals from more than 10 families reported, supportive functional data including animal models.

New HGNC name is PJVK.
Deafness_IsolatedAndComplex v0.449 DFNB59 Zornitza Stark reviewed gene: DFNB59: Rating: GREEN; Mode of pathogenicity: None; Publications: 16804542, 26166082, 22617256, 28964305, 17373699, 25631766, 28209736; Phenotypes: Deafness, autosomal recessive 59, MIM# 610220; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.449 DFNB59 Zornitza Stark Tag new gene name tag was added to gene: DFNB59.
Deafness_IsolatedAndComplex v0.0 DFNB59 Zornitza Stark gene: DFNB59 was added
gene: DFNB59 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: DFNB59 was set to Unknown