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Zinc finger MYM-type protein 6 (ZMYM6) is a protein-coding gene located on chromosome 1 that encodes a member of the MYM-type zinc finger protein family. ZMYM6 plays a critical role in maintaining cell shape and organizing the cytoskeletal network, and is predicted to participate in DNA binding and regulation of cell morphogenesis. It is predominantly nuclear and is associated with biological processes such as cytoskeleton organization. Diseases linked to ZMYM6 include non-syndromic X-linked intellectual disability, but no direct therapeutic targeting, approved biomarkers, or interacting drugs have been established to date.
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