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Menin is a nuclear scaffold protein encoded by the MEN1 gene. It functions as a regulator of gene transcription, chromatin remodeling, and epigenetic control of gene expression. Menin is best known for its role as a tumor suppressor and its association with multiple endocrine neoplasia type 1 (MEN-1) syndrome. Loss-of-function mutations in MEN1 lead to disrupted cell cycle control mechanisms and increased risk of tumor formation, especially within endocrine tissues.
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