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MORN repeat-containing protein 4 (MORN4) is a protein characterized by multiple MORN (Membrane Occupation and Recognition Nexus) repeats, which function as specific protein-binding modules that recognize and bind protein cargoes such as the tail of myosin 3a[1]. It forms an extended single-layered β-sheet with a U-shaped groove for high-affinity, specific binding. MORN4 is located in the cytoplasm and filopodium tip and has been implicated in promoting axonal degeneration following neuronal injury due to toxic insult or trauma[3][5][6]. Diseases associated with mutations in MORN4 include autosomal recessive nonsyndromic deafness and Deafness, Autosomal Recessive 30[3]. There is currently no evidence that MORN4 is a therapeutic target, nor are there known interacting drugs or safety concerns described.
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