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Keratin 19 pseudogene 3 (KRT19P3) is a non-protein-coding pseudogene highly homologous to the functional KRT19 (keratin 19) gene, located within the type I keratin gene family on chromosome 17. Unlike true keratin genes, KRT19P3 contains deletions and mutations (including frameshifts and premature termination codons), rendering it non-functional. Its main relevance is as a source of potential analytical error in diagnostic assays (RT-PCR) for cancer, because it may be mistaken for KRT19 mRNA in blood or tissue samples, resulting in false positive detection of micrometastatic disease[4][8]. There is no evidence that KRT19P3 has any structural, enzymatic, or receptor function, nor is it considered a therapeutic target.
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