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Family with sequence similarity 246 member B (FAM246B) is a human protein-coding gene with limited functional characterization. It encodes the protein FAM246B. Current evidence does not support a characterized role as a receptor, enzyme, transporter, or other classic drug target, and there are no known substrates or biological mechanisms described for this protein. The gene has been associated with certain diseases, such as Autism Spectrum Disorder, based on genetic studies, but the functional relationship and mechanism are unknown. No drugs are known to interact with this protein, and there are no established uses as a biomarker or safety concerns described in the literature.
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