👉 The term "homocerebrin" is typically used to describe a protein that is predominantly found in the brains of individuals with a genetic disorder called Fragile X Syndrome (FZS). It is an abnormal protein that cannot be properly synthesized or transported, leading to a variety of symptoms and conditions. In FZS, the homocerebrin protein plays a crucial role in several cellular processes. One of its primary functions is to serve as a signaling molecule between cells, particularly neurons