GCK

glucokinase
OMIM: 138079, Gene2Phenotype

8 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 8 panels
Green GCK in Hyperinsulinism Level 2: Endocrine disorders Version 1.49	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes 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)
Green GCK in Mendeliome Version 1.3499	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes 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)
Red GCK in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.398	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red Genetic Health Queensland Phenotypes Diabetes mellitus, permanent neonatal 606176
Green GCK in Maturity-onset Diabetes of the Young Level 2: Endocrine disorders Version 1.24	2 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green Royal Melbourne Hospital Phenotypes 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)
Green GCK in Monogenic Diabetes Level 2: Endocrine disorders Version 0.152 Component of the following Super Panels: Metabolic Disorders Superpanel	1 review	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Phenotypes 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)
Green GCK in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources BabySeq Category A gene Expert Review Green Phenotypes Hyperinsulinemic hypoglycemia, familial
Green GCK in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	2 reviews	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green BabySeq Category A gene BeginNGS Phenotypes Hyperinsulinemic hypoglycemia, familial, MIM#602485 Tags treatable endocrine
Green GCK in Transplant Co-Morbidity Level 2: Screening Version 0.20	0 reviews	BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Phenotypes Hyperinsulinemic hypoglycemia, familial, 3, AD (MIM#602485) MODY, type II, AD (MIM#125851) Diabetes mellitus, permanent neonatal 1, AR (MIM#606176) Diabetes mellitus, noninsulin-dependent, late onset, AD (MIM#125853)