{{Rsnum
|rsid=80356655
|Chromosome=7
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GCK
|position=44147830
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GCK
}}{{omim
|id=138079
|rsnum=80356655
|variant=0003
}}{{ClinVar
|rsid=80356655
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=44187429
|CHROM=7
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=GCK:2645
|GENE_NAME=GCK
|GENE_ID=2645
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.44187429G>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1447; 138079.0003; 138079.0011
|CLNSIG=5
|CLNCUI=C1841962
|CLNDBN=MATURITY-ONSET DIABETES OF THE YOUNG, TYPE II; Maturity-onset diabetes of the young, type 2; Permanent neonatal diabetes mellitus
|Disease=MATURITY-ONSET DIABETES OF THE YOUNG; Maturity-onset diabetes of the young; Permanent neonatal diabetes mellitus
|CLNACC=RCV000017514.26; RCV000020167.1; RCV000030923.26
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1447:C1841962:125851:552; NBK1447:C1833104:606176:79134:99885
}}{{PMID Auto
|PMID=1502186
|Title=Human glucokinase gene: isolation, characterization, and identification of two missense mutations linked to early-onset non-insulin-dependent (type 2) diabetes mellitus.
|OA=1
}}

{{PMID Auto
|PMID=11372010
|Title=Neonatal diabetes mellitus due to complete glucokinase deficiency.
}}