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Ribosomal protein S26 pseudogene 21 (RPS26P21) is one of many processed pseudogenes of the ribosomal protein S26 (RPS26) gene in the human genome[3][4][6][8]. Pseudogenes arise from the duplication and reverse transcription of functional genes but typically acquire disabling mutations that prevent them from encoding functional proteins[4]. RPS26P21 is not believed to express any protein or have a defined biological function. The functional gene RPS26 encodes a component of the small (40S) ribosomal subunit and is vital for protein synthesis, with mutations in RPS26 causing Diamond-Blackfan anemia, but the pseudogene does not share these disease roles[5][7][9].
Not applicable. No drugs act via this pseudogene
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