The search for interactive proteins and phosphorylation targets linked to FAM20C in the nervous system paved the way for a deeper understanding of the pathophysiological underpinnings of neurological disorders associated with FAM20C, including treatment‐resistant depression [24], Raine syndrome, and familial cerebral small vessel disease [25]. The gene discussed is FAM20C; the disease is lethal osteosclerotic bone dysplasia.