{{Rsnum
|rsid=80356611
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=KCNJ11
|position=17387943
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ11
}}{{omim
|id=600937
|rsnum=80356611
|variant=0006
}}{{ClinVar
|rsid=80356611
|Reversed=1
|FwdREF=G
|FwdALT=A,C
|REF=C
|ALT=G,T
|RSPOS=17409490
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=KCNJ11:3767
|GENE_NAME=KCNJ11
|GENE_ID=3767
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000011.9:g.17409490C>G; NC_000011.9:g.17409490C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=
NBK1447; 600937.0006
|CLNSIG=5
|CLNCUI=
|CLNDBN=Permanent neonatal diabetes mellitus; Neonatal diabetes mellitus
|Disease=Permanent neonatal diabetes mellitus; Neonatal diabetes mellitus
|CLNACC=
RCV000009205.2; RCV000030103.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet; MedGen:SNOMED_CT
|CLNDSDBID=NBK1447:C1833104:606176:79134:99885; C0158981:49817004
}}{{PMID Auto
|PMID=16636
|Title=Rapid formation of carcinogenic N-nitrosamines in aqueous alkaline solutions.
|OA=1
}}

{{PMID Auto
|PMID=15561897
|Title=Toward linking structure with function in ATP-sensitive K+ channels.
}}

{{PMID Auto
|PMID=16731833
|Title=Mutations at the same residue (R50) of Kir6.2 (KCNJ11) that cause neonatal diabetes produce different functional effects.
}}

{{PMID Auto
|PMID=16885550
|Title=Switching from insulin to oral sulfonylureas in patients with diabetes due to Kir6.2 mutations.
}}

{{PMID Auto
|PMID=17635943
|Title=Molecular basis of neonatal diabetes in Japanese patients.
}}

{{PMID Auto
|PMID=18767144
|Title=Update of mutations in the genes encoding the pancreatic beta-cell K(ATP) channel subunits Kir6.2 (KCNJ11) and sulfonylurea receptor 1 (ABCC8) in diabetes mellitus and hyperinsulinism.
}}{{PMID Auto
|PMID=15580558
|Title=KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.
}}