Activity

Filter

Cancel
Date Panel Item Activity
8 actions
Genomic screening in children: BabyScreen+ v0.83 GCK Zornitza Stark Tag treatable tag was added to gene: GCK.
Tag endocrine tag was added to gene: GCK.
Genomic screening in children: BabyScreen+ v0.78 GCK Zornitza Stark Marked gene: GCK as ready
Genomic screening in children: BabyScreen+ v0.78 GCK Zornitza Stark Gene: gck has been classified as Green List (High Evidence).
Genomic screening in children: BabyScreen+ v0.78 GCK Zornitza Stark Phenotypes for gene: GCK were changed from Diabetes mellitus, noninsulin-dependent, late onset, AD (MIM#125853); Diabetes mellitus, permanent neonatal 1, AR (MIM#606176); Hyperinsulinemic hypoglycemia, familial, 3, AD (MIM#602485); MODY, type II, AD (MIM#125851) to MODY, type II, AD (MIM#125851)
Genomic screening in children: BabyScreen+ v0.77 GCK Zornitza Stark Mode of inheritance for gene: GCK was changed from BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genomic screening in children: BabyScreen+ v0.76 GCK Zornitza Stark reviewed gene: GCK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: MODY, type II, AD (MIM#125851); Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genomic screening in children: BabyScreen+ v0.68 Zornitza Stark Copied gene GCK from panel Maturity-onset Diabetes of the Young
Genomic screening in children: BabyScreen+ v0.68 GCK Zornitza Stark gene: GCK was added
gene: GCK was added to Genomic screening in children: BabyScreen+. Sources: Expert Review Green,Royal Melbourne Hospital
Mode of inheritance for gene: GCK was set to BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Publications for gene: GCK were set to 19790256
Phenotypes for gene: GCK were set to Diabetes mellitus, noninsulin-dependent, late onset, AD (MIM#125853); Diabetes mellitus, permanent neonatal 1, AR (MIM#606176); Hyperinsulinemic hypoglycemia, familial, 3, AD (MIM#602485); MODY, type II, AD (MIM#125851)