Numerous non-neuronal tau inclusions characterize human tauopathy diseases, including coiled bodies in oligodendrocytes and several variations of astrocytic inclusions, while there is very little evidence of microglia accumulating tau pathology (Ikeda et al., 1998; Arai et al., 2001; Ghoshal et al., 2001; Ferrer et al., 2014). The gene discussed is MAPT; the disease is tauopathy.