Target intelligence / Profile preview

Ribosomal protein L17 pseudogene 23 (RPL17P23)

Target
RPL17P23
Molecular classification
Other (Pseudogene)
01

Overview

RPL17P23 (ribosomal protein L17 pseudogene 23) is a non-coding pseudogene in the human genome, related by sequence similarity to the ribosomal protein L17 (RPL17), which is a structural component of the 60S ribosomal subunit required for protein synthesis[1][5]. Pseudogenes like RPL17P23 arise from duplication or retrotransposition events and do not encode active protein products. While some pseudogenes have emerging roles as gene regulators or disease modifiers, RPL17P23 does not have established biological or pathological functions. There is no evidence that it is a therapeutic target or involved in direct disease mechanisms. It is sometimes referenced in genomic annotation studies but is largely considered of limited functional significance in most biomedical contexts[1][5]. Key clarification: - RPL17P23 should not be confused with the functional ribosomal protein L17 (RPL17), which is a structural ribosomal protein and has been implicated in biological processes such as stress vulnerability, depression, and ribosomopathies[7][4]. - Pseudogenes like RPL17P23 are generally excluded from drug target lists and clinical databases due to their lack of protein-coding and direct biochemical activity[1][5].

Other names
RPL17_15_751RPL17P23
02

Mechanism of action

None. There are no drugs targeting this pseudogene, thus no mechanism of action is described.

03

Biological functions

Other (no established biological function; possible regulatory role, as some pseudogenes may affect gene expression of related genes but this is not well defined for RPL17P23)
04

Disease associations

Other. No direct evidence links RPL17P23 to disease. However, aberrant pseudogene expression has been noted in cancer contexts for related ribosomal pseudogenes, but RPL17P23 itself does not have a specific disease association

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