Activity

Filter

Cancel
Date Panel Item Activity
9 actions
Glucokinase-related fasting hyperglycaemia v1.2 GCK Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIMs #125851, #125853, #602485 & #606176) and these OMIM records were last accessed on 19 December 2025.
Glucokinase-related fasting hyperglycaemia v1.2 GCK Achchuthan Shanmugasundram Phenotypes for gene: GCK were changed from to MODY, type II, OMIM:125851; Diabetes mellitus, noninsulin-dependent, late onset, OMIM:125853; Hyperinsulinemic hypoglycemia, familial, 3, OMIM:602485; Diabetes mellitus, permanent neonatal 1, OMIM:606176; maturity-onset diabetes of the young type 2, MONDO:0007453; permanent neonatal diabetes mellitus 1, MONDO:0100165; hyperinsulinism due to glucokinase deficiency, MONDO:0011236
Glucokinase-related fasting hyperglycaemia v1.1 Eleanor Williams Panel version 1.0 has been signed off on 2023-09-14
Glucokinase-related fasting hyperglycaemia v1.0 Eleanor Williams promoted panel to version 1.0
Glucokinase-related fasting hyperglycaemia v0.3 Eleanor Williams Panel types changed to GMS Rare Disease; GMS signed-off
Glucokinase-related fasting hyperglycaemia v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Glucokinase-related fasting hyperglycaemia v0.1 GCK Achchuthan Shanmugasundram reviewed gene: GCK: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Glucokinase-related fasting hyperglycaemia v0.1 GCK Achchuthan Shanmugasundram gene: GCK was added
gene: GCK was added to Glucokinase-related fasting hyperglycaemia. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: GCK was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Glucokinase-related fasting hyperglycaemia v0.0 Achchuthan Shanmugasundram Added Panel Glucokinase-related fasting hyperglycaemia
Set list of related panels to R142
Set panel types to: GMS Rare Disease