ADNP showed relatively reduced expression in the ADNP syndrome cerebellum, which was also observed for 25 additional genes (representing >50% of the tested genes), including NLGN1, NLGN2, PAX6, SMARCA4, and SNAP25, converging on nervous system development and tauopathy. The gene discussed is NLGN2; the disease is ADNP-related multiple congenital anomalies - intellectual disability - autism spectrum disorder.