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Metadherin pseudogene

Molecular classification
Pseudogene, Non-coding RNA (if transcribed)
01

Overview

Metadherin pseudogene" (ENSG00000269471) designates a **pseudogene** that shares sequence similarity with the protein-coding metadherin (MTDH) gene but is not itself a functional protein-coding gene. Pseudogenes are considered genomic relics; they arise from duplication or retrotransposition events and acquire mutations that prevent productive transcription or translation[1][3][5]. While most pseudogenes are thought to be non-functional, some have regulatory roles as noncoding RNAs, potentially influencing the expression of their parent genes[3][5]. The metadherin pseudogene does not encode the functional Metadherin protein implicated in cancer and other pathologies, and is not itself considered a therapeutic target or receptor[1][3]. The term "metadherin pseudogene" does **not** refer to the actively studied cancer target "Metadherin" (also known as MTDH/AEG-1/LYRIC)[2][6][10][12]. ENSG00000269471 is a non-functional sequence related to metadherin and should not be considered a direct therapeutic target[1][3]. Pseudogenes, by definition, usually do **not** code for active proteins or canonical drug targets (like receptors, enzymes, or channels), although rare exceptions exist when regulatory function is proven[1][3][5]. For drug targets and disease association, the relevant locus is MTDH (ENSG00000147649), not the pseudogene[2][10][12]. ENSG00000269471 is a non-coding pseudogene, not a therapeutic target, and should be flagged as "is_incorrect: true" when targeted for drug discovery, assay design, or biomarker analysis. Most drug, function, and disease association information in the literature pertains to the true metadherin gene (MTDH), not its pseudogene.

02

Biological functions

Possible regulatory roles as a non-coding RNA (e.g., acting as a microRNA decoy or regulating gene expression)
03

Disease associations

Other (pseudogenes generally do not have direct, well-documented disease roles, but some may influence disease indirectly as regulatory elements)

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