Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Moldiag Diseases Genes Support Contact

MODY10 diabetes

MODY10 is an autosomal dominant early-onset type 2 diabetes caused by mutations of the proinsulin gene (INS).

Systematic

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

References:

1.

Edghill EL et al. (2008) Insulin mutation screening in 1,044 patients with diabetes: mutations in the INS gene are a common cause of neonatal diabetes but a rare cause of diabetes diagnosed in childhood or adulthood.

external link
2.

Molven A et al. (2008) Mutations in the insulin gene can cause MODY and autoantibody-negative type 1 diabetes.

external link
3.

OMIM.ORG article

Omim 613370 external link
Update: Aug. 14, 2020
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