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High mobility group nucleosomal binding domain 2 pseudogene 8 (HMGN2P8) is a processed human pseudogene located on chromosome 16. As a pseudogene, it originated from a retrotransposition event, resulting in a nonfunctional, intronless paralog of the HMGN2 gene[6][4]. It does not encode a functional protein and is not known to have a direct biological or therapeutic role. While some pseudogenes can regulate other genes via noncoding RNAs, there is currently no direct evidence that HMGN2P8 has such regulatory function or relevance as a biomarker, drug target, or risk gene[2][3][6]. Its known aliases include AC022394.1 and HMGN2L8[1][3].
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