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Deafness_IsolatedAndComplex v0.539 WFS1 Zornitza Stark Marked gene: WFS1 as ready
Deafness_IsolatedAndComplex v0.539 WFS1 Zornitza Stark Gene: wfs1 has been classified as Green List (High Evidence).
Deafness_IsolatedAndComplex v0.539 WFS1 Zornitza Stark Phenotypes for gene: WFS1 were changed from to Deafness, autosomal dominant 6/14/38, MIM# 600965; Wolfram syndrome 1 222300; Wolfram-like syndrome, autosomal dominant, MIM# 614296
Deafness_IsolatedAndComplex v0.538 WFS1 Zornitza Stark Publications for gene: WFS1 were set to
Deafness_IsolatedAndComplex v0.537 WFS1 Zornitza Stark Mode of inheritance for gene: WFS1 was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.536 WFS1 Zornitza Stark edited their review of gene: WFS1: Changed publications: 11709537, 12073007, 16648378, 18544103, 20069065, 21538838, 25250959, 27395765, 28802351, 29529044, 12754709, 16151413, 21446023, 21602428
Deafness_IsolatedAndComplex v0.536 WFS1 Zornitza Stark reviewed gene: WFS1: Rating: GREEN; Mode of pathogenicity: None; Publications: 11709537, 12073007, 16648378, 18544103, 20069065, 21538838, 25250959, 27395765, 28802351, 29529044; Phenotypes: Deafness, autosomal dominant 6/14/38, MIM# 600965, Wolfram syndrome 1 222300, Wolfram-like syndrome, autosomal dominant, MIM# 614296; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.0 WFS1 Zornitza Stark gene: WFS1 was added
gene: WFS1 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: WFS1 was set to Unknown