As a possible cause of MODY subtypes 7–14, eight genes have been suggested: Kruppel-like factor 11 (KLF11); carboxyl ester lipase; paired-box-containing gene 4 (PAX4); insulin (INS); B-lymphocyte kinase; adenosine triphosphate (ATP)-binding cassette, sub-family C (CFTR/MRP) number 8 (ABCC8); potassium channel, inwardly rectifying subfamily J, member 11 (KCNJ11); adaptor protein, phosphotyrosine interaction, PH domain, and leucine zipper containing (APPL1) [27]. The gene discussed is KCNJ11; the disease is MODY.