Activity

Filter

Cancel
Date Panel Item Activity
12 actions
Deafness_IsolatedAndComplex v0.41 CLIC5 Zornitza Stark Marked gene: CLIC5 as ready
Deafness_IsolatedAndComplex v0.41 CLIC5 Zornitza Stark Gene: clic5 has been classified as Amber List (Moderate Evidence).
Deafness_IsolatedAndComplex v0.41 CLIC5 Zornitza Stark Phenotypes for gene: CLIC5 were changed from Deafness, autosomal recessive 103, MIM# 616042 to Deafness, autosomal recessive 103, MIM# 616042
Deafness_IsolatedAndComplex v0.40 CLIC5 Zornitza Stark Phenotypes for gene: CLIC5 were changed from Deafness, autosomal recessive 103, MIM# 616042 to Deafness, autosomal recessive 103, MIM# 616042
Deafness_IsolatedAndComplex v0.39 CLIC5 Zornitza Stark Phenotypes for gene: CLIC5 were changed from to Deafness, autosomal recessive 103, MIM# 616042
Deafness_IsolatedAndComplex v0.39 CLIC5 Zornitza Stark Publications for gene: CLIC5 were set to 24781754; 17021174
Deafness_IsolatedAndComplex v0.38 CLIC5 Zornitza Stark Publications for gene: CLIC5 were set to
Deafness_IsolatedAndComplex v0.38 CLIC5 Zornitza Stark Mode of inheritance for gene: CLIC5 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.37 CLIC5 Zornitza Stark Classified gene: CLIC5 as Amber List (moderate evidence)
Deafness_IsolatedAndComplex v0.37 CLIC5 Zornitza Stark Gene: clic5 has been classified as Amber List (Moderate Evidence).
Deafness_IsolatedAndComplex v0.36 CLIC5 Zornitza Stark reviewed gene: CLIC5: Rating: AMBER; Mode of pathogenicity: None; Publications: 24781754, 17021174; Phenotypes: Deafness, autosomal recessive 103, MIM# 616042; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Deafness_IsolatedAndComplex v0.0 CLIC5 Zornitza Stark gene: CLIC5 was added
gene: CLIC5 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: CLIC5 was set to Unknown