In T1DM, some of the terms annotated were related to myelin dysregulation (ARHGEF6, CNP, NADK2, PSAP, SLC25A12) and other neurological disorders, such as Alzheimer’s disease (i.e., POA2, APOC1, APOC3, CNP, GSK3B, PON1, PSAP, SELENBP1) or movement disorders (Table 2). The gene discussed is SELENBP1; the disease is type 1 diabetes mellitus.