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Dynein heavy chain domain-containing protein 1 (DNHD1) is a microtubule motor protein localizing to the sperm flagellum, where it contributes to the assembly and structural organization of the axoneme, crucial for sperm motility and fertility. Genetic mutations in DNHD1 cause severe flagellar abnormalities—such as disorganization, absence of the central pair complex, and mitochondrial sheath malformation—leading to male infertility with the multiple morphological abnormalities of the sperm flagellum (MMAF) phenotype. DNHD1 has binding activity for dynein intermediate and light chains, supporting its role in assembling flagellar motor complexes. DNHD1 is not currently a recognized therapeutic target, but its mutation status can serve as a genetic biomarker for the diagnosis of certain infertility syndromes.
Not applicable; no drugs are reported to interact with DNHD1.
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