GNAO1 and Encephalopathy: A large amount of clinically oriented literature reports on the pathophysiological effects of GNAO1 (the common gene for both Gαo1 and Gαo2) mutations leading to so‐called GNAO1 encephalopathies including symptoms such as epilepsy, movement disorders, developmental delay, or intellectual disability (Ludlam et al., 2024).