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Cytochrome c pseudogene 39 (CYCSP39, also called HC1 or HCP39) is one of 49 cytochrome c pseudogenes identified in the human genome. These pseudogenes originated from retrotransposition events, meaning genetic material from the cytochrome c gene was copied and inserted back into the genome as non-functional copies. Most cytochrome c pseudogenes, including CYCSP39, contain disablements such as frame shifts and premature stop codons, and none are normally expressed as proteins in humans. While some pseudogenes in other families have become key regulators or disease-related, CYCSP39 has no documented biological function, disease association, or therapeutic relevance. Its primary importance is as a component of the molecular record for cytochrome c gene evolution in primates.
None; drug mechanisms do not target pseudogenes directly
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