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High mobility group box 1 pseudogene 27 (HMGB1P27) is a human pseudogene located within the genome and classified in the NCBI Gene database[4]. By definition, pseudogenes are DNA sequences resembling functional genes but which have lost the ability to encode functional proteins due to mutations, regulatory changes, or incomplete transcription/translation[5]. While some pseudogenes in other gene families may exert regulatory effects at the RNA level (for example, by acting as miRNA sponges or influencing parent gene expression[2][3]), there is currently no published evidence for functional involvement of HMGB1P27 in human disease, biological processes, or drug interactions. Thus, HMGB1P27 should not be considered a canonical therapeutic target.
None. There is no described mechanism of action for drugs targeting HMGB1P27.
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