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Cholestasis v0.208 ADK Zornitza Stark Publications for gene: ADK were set to 21963049; 17120046
Cholestasis v0.207 ADK Zornitza Stark Classified gene: ADK as Green List (high evidence)
Cholestasis v0.207 ADK Zornitza Stark Gene: adk has been classified as Green List (High Evidence).
Cholestasis v0.206 ADK Zornitza Stark edited their review of gene: ADK: Added comment: Additional cases with neonatal cholestasis.; Changed rating: GREEN; Changed publications: 21963049, 17120046, 33309011
Cholestasis v0.42 ADK Zornitza Stark Marked gene: ADK as ready
Cholestasis v0.42 ADK Zornitza Stark Gene: adk has been classified as Red List (Low Evidence).
Cholestasis v0.42 ADK Zornitza Stark Phenotypes for gene: ADK were changed from to Hypermethioninemia due to adenosine kinase deficiency, MIM# 614300
Cholestasis v0.41 ADK Zornitza Stark Publications for gene: ADK were set to
Cholestasis v0.40 ADK Zornitza Stark Mode of inheritance for gene: ADK was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Cholestasis v0.39 ADK Zornitza Stark Classified gene: ADK as Red List (low evidence)
Cholestasis v0.39 ADK Zornitza Stark Gene: adk has been classified as Red List (Low Evidence).
Cholestasis v0.38 ADK Zornitza Stark reviewed gene: ADK: Rating: RED; Mode of pathogenicity: None; Publications: 21963049, 17120046; Phenotypes: Hypermethioninemia due to adenosine kinase deficiency, MIM# 614300; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cholestasis v0.0 ADK Zornitza Stark gene: ADK was added
gene: ADK was added to Cholestasis_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ADK was set to Unknown