Human Myosin-Ib (MYO1B) ELISA Kit

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 Delta508-CFTR traffic / ER-to-Golgi in CF. GO annotations related to this gene include calmodulin binding and motor activity. An important paralog of this gene is MYO1A. Motor protein that may participate in process critical to neuronal development and function such as cell migration, neurite outgrowth and vesicular transport.