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60S ribosomal protein L38 (RPL38) is a structural component of the large (60S) subunit of the eukaryotic ribosome, encoded by the RPL38 gene on chromosome 17. It is part of the L38E family, located in the cytoplasm, and participates in catalyzing cellular protein synthesis during translation. It does not have a direct enzymatic or receptor-related role and is not targeted by current therapeutics. Mutations in animal models cause anemia, skeletal malformations, and hearing loss but in humans, no pathogenic mutations have been definitively linked to disease.
Not applicable; no drugs are known to act specifically on this protein.
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