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Chromodomain Y-linked 22 pseudogene (CDY22P) is a duplicated pseudogene on human chromosome 22, derived from the family of chromodomain Y-linked (CDY) genes present on the Y chromosome[1]. Pseudogenes are traditionally classified as nonfunctional genomic relics but are now recognized to sometimes produce noncoding RNAs with regulatory activity in specific genetic or disease contexts[4][6]. While some chromosome 22 pseudogenes show transcriptional activity, strong evidence for functional protein product or clinical relevance for CDY22P does not exist[1]. No therapeutic drugs target this pseudogene, and it is not considered a receptor, enzyme, transporter, or other classical drug target. The main relevance of the region is for research into genome structure, pseudogene evolution, and rare regulatory phenomena.
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