Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders

MODY13 diabetes

MODY13 is an autosomal dominant early-onset type 2 diabetes caused by mutations of the KCNJ11 gene.

Systematic

MODY diabetes
MODY1 diabetes
MODY10 diabetes
MODY11 diabetes
MODY12 diabetes
MODY13 diabetes
KCNJ11
MODY14 diabetes
MODY2 diabetes
MODY3 diabetes
MODY4 diabetes
MODY5 diabetes
MODY6 diabetes
MODY7 diabetes
MODY8 diabetes
MODY9 diabetes

References:

1.

Yorifuji T et al. (2005) The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus.

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2.

Prudente S et al. (2015) Loss-of-Function Mutations in APPL1 in Familial Diabetes Mellitus.

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3.

Bonnefond A et al. (2012) Whole-exome sequencing and high throughput genotyping identified KCNJ11 as the thirteenth MODY gene.

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4.

OMIM.ORG article

Omim 616329 [^]
Update: April 29, 2019