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The "Apolipoprotein C-IV–apolipoprotein C-II readthrough (NMD candidate)" transcript results from read-through transcription between the adjacent APOC4 and APOC2 genes on chromosome 19. It is classified as a candidate for nonsense-mediated mRNA decay, and therefore, it is unlikely to be translated into a functional protein. There is no evidence supporting a physiological or pharmacological role for this readthrough transcript, and it is not considered a receptor, enzyme, transporter, or other canonical drug target[1][3]. Disease phenotypes and functional roles attributed to this genomic region are due to the parental APOC2 and APOC4 genes, not to the readthrough product itself.
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