{{Rsnum
|rsid=193922272
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=GCK
|position=44145510
|Gene_s=GCK
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=193922272
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=44185109
|CHROM=7
|dbSNPBuildID=136
|SSR=0
|SAO=1
|VP=0x050268000000000002100100
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.44185109T>C
|CLNSRC=Correlagen
|CLNORIGIN=1
|CLNSIG=4
|CLNDBN=Maturity-onset diabetes of the young, type 2
|Disease=Maturity-onset diabetes of the young
|Tags=RV;PM;PMC;S3D;OTHERKG;LSD
|CLNACC=RCV000029851.1
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1447:C1841962:125851:552
|GENEINFO=GCK:2645
|GENE_ID=2645
|GENE_NAME=GCK
}}{{PMID Auto
|PMID=7542040
|Title=Characterization of Japanese families with early-onset type 2 (non-insulin dependent) diabetes mellitus and screening for mutations in the glucokinase and mitochondrial tRNA(Leu(UUR)) genes.
}}

{{PMID Auto
|PMID=8433729
|Title=Familial hyperglycemia due to mutations in glucokinase. Definition of a subtype of diabetes mellitus.
}}

{{PMID Auto
|PMID=8446612
|Title=Glucokinase mutations associated with non-insulin-dependent (type 2) diabetes mellitus have decreased enzymatic activity: implications for structure/function relationships.
|OA=1
}}

{{PMID Auto
|PMID=10525657
|Title=Mutants of glucokinase cause hypoglycaemia- and hyperglycaemia syndromes and their analysis illuminates fundamental quantitative concepts of glucose homeostasis.
}}

{{PMID Auto
|PMID=14517946
|Title=Glucokinase (GCK) mutations in hyper- and hypoglycemia: maturity-onset diabetes of the young, permanent neonatal diabetes, and hyperinsulinemia of infancy.
}}

{{PMID Auto
|PMID=17353190
|Title=Glucokinase thermolability and hepatic regulatory protein binding are essential factors for predicting the blood glucose phenotype of missense mutations.
}}