Prions are best described in the context of human-centric neurodegenerative diseases such as Kuru and Creutzfeldt-Jakob, as well as Alzheimer and Parkinson diseases [35], which are principally thought to be caused mainly by rogue proteins of specific natures; what is remarkable is that PrPs are encoded in the host’s genome [36]. The gene discussed is MSMB; the disease is neurodegenerative disease.