STX2 (Syntaxin 2) is a Protein Coding gene. Diseases associated with STX2 include Osteogenesis Imperfecta, Type Xv and Deafness, Autosomal Dominant 41. Among its related pathways are Sertoli-Sertoli Cell Junction Dynamics and Synaptic vesicle cycle. The product of STX2 belongs to the syntaxin/epimorphin family of proteins. The syntaxins are a large protein family implicated in the targeting and fusion of intracellular transport vesicles. The product of STX2 regulates epithelial-mesenchymal interactions and epithelial cell morphogenesis and activation. Alternatively spliced transcript variants encoding different isoforms have been identified.
