{{Rsnum
|rsid=80356616
|Chromosome=11
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=KCNJ11
|position=17387917
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=KCNJ11
}}{{omim
|id=600937
|rsnum=80356616
|variant=0003
}}{{ClinVar
|rsid=80356616
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=17409464
|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
|CLNHGVS=NC_000011.9:g.17409464C>T
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=NBK1447; 600937.0003
|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=RCV000009201.2; RCV000030665.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=MedGen; GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=C1833102; NBK1447:C1833104:606176:79134:99885
}}{{PMID|15115830}} Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes.

{{PMID|15580558}} KCNJ11 activating mutations in Italian patients with permanent neonatal diabetes.

{{PMID|15583126|OA=1
}} Molecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological features.

{{PMID|16123337}} Activating mutations in Kir6.2 and neonatal diabetes: new clinical syndromes, new scientific insights, and new therapy.

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