HNF1B and MODY: They have had some utility in providing support for hypotheses relating to mechanism and expression patterns for specific genes, particularly in MODY caused by mutations in the transcription factors hepatocyte nuclear factor 1 alpha (HNF-1A) [42, 43] and hepatocyte nuclear factor 1 beta (HNF-1B) [44] and in neonatal diabetes due to KCNJ11 mutations [45–47].