{{Rsnum
|rsid=80356618
|Chromosome=11
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=KCNJ11
|position=17387595
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ11
}}{{omim
|id=600937
|rsnum=80356618
|variant=0015
}}{{ClinVar
|rsid=80356618
|Reversed=1
|FwdREF=G
|FwdALT=A,T
|REF=C
|ALT=A,T
|RSPOS=17409142
|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.17409142C>A; NC_000011.9:g.17409142C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1447; 600937.0015
|CLNSIG=5
|CLNCUI=C1833104; C1833104
|CLNDBN=Diabetes mellitus, permanent neonatal, with neurologic features; Permanent neonatal diabetes mellitus
|Disease=Diabetes mellitus; Permanent neonatal diabetes mellitus
|CLNACC=RCV000009216.1; RCV000020352.1; RCV000020351.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1833102; NBK1447:C1833104:606176:79134:99885
}}{{PMID Auto
|PMID=16416420
|Title=Mutations in the genes encoding the pancreatic beta-cell KATP channel subunits Kir6.2 (KCNJ11) and SUR1 (ABCC8) in diabetes mellitus and hyperinsulinism.
}}

{{PMID Auto
|PMID=16670688
|Title=KCNJ11 activating mutations are associated with developmental delay, epilepsy and neonatal diabetes syndrome and other neurological features.
}}