Several significantly changed genes at this timepoint have been associated with AD-like pathology and disease progression (BCL2L2, CHST8, CLEC7A, CYP27A, CYP7B1, DAPK1, GPR34, MERTK, OLFML3, SUMO1, TTR, TYROBP), cognitive impairment (DAPK1, EXO1, RELN, SUMO1, TYROBP), PD progression (SUMO1, MAPK10), and the accumulation of toxic proteins (DAPK1, MAPK10, MSR1, OLFML3, SUMO1, TYROBP). Here, CLEC7A is linked to Parkinson disease.