Clinical feature: 

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

Literature: 

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