MYO1B (Myosin IB) is a Protein Coding gene. Diseases associated with MYO1B include Glass Syndrome and Amebiasis. Among its related pathways are Sertoli-Sertoli Cell Junction Dynamics and Actin Nucleation by ARP-WASP Complex. Motor protein that may participate in process critical to neuronal development and function such as cell migration, neurite outgrowth and vesicular transport.
