General Information:

Id: 2,578 (click here to show other Interactions for entry)
Diseases: Diabetes mellitus, type II - [OMIM]
Insulin resistance
Reference: Lang V et al.(2011) The molecular genetics of sulfonylurea receptors in the pathogenesis and treatment of insulin secretory disorders and type 2 diabetes Curr. Diab. Rep. 11: 543-551 [PMID: 21968738]

Interaction Information:

Comment Genetic mutations in the KCNJ11 and ABCC8 genes have been linked to persistent hyperinsulinemic hypoglycemia of infancy (PHHI) and neonatal diabetes (ND).
Formal Description
Interaction-ID: 24300



affects_activity of

Drugbank entries Show/Hide entries for ABCC8