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COX20 pseudogene 1 (COX20P1) is a noncoding genomic locus classified as a pseudogene derived from the COX20 gene, which encodes a mitochondrial chaperone involved in ataxia and mitochondrial complex IV assembly[2][4]. Pseudogenes, including COX20P1, do not encode functional proteins and are generally considered evolutionary relics, although a minority may play regulatory roles in rare cases[1][3]. There are currently no reports of COX20P1 being involved in any physiological or pathogenic process, nor is it recognized as a drug or disease target in clinical or biomedical literature.
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