Ribosomal protein L17 pseudogene 52 (RPL17P52)

Ribosomal protein L17 pseudogene 52 (RPL17P52) is a processed pseudogene found in the human genome, related by sequence homology to the functional RPL17 gene, which encodes ribosomal protein L17[1][3][4]. Processed pseudogenes are genomic DNA segments derived from mRNA retrotransposition events and do not typically encode functional proteins due to disablements such as stop codons and frameshifts[3]. RPL17P52, like other ribosomal protein pseudogenes, is located throughout the genome without known regulatory or protein-coding function. Unlike its parent RPL17 gene, which participates in ribosomal structure and function, the pseudogene variant is not involved in normal protein synthesis, cellular signaling, disease, or therapeutic pathways[1][3]. It has no recognized biological activity, does not interact with drugs, nor serve as a biomarker, and is not considered a therapeutic target. If you require information about the parent, protein-coding RPL17 gene (Ribosomal protein L17), or its biological/pathological significance, that would be a distinct query since RPL17P52 itself is non-functional[2].

Other names

Ribosomal protein L17 pseudogene 52RPL17P52