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FTLP4 (Ferritin light chain pseudogene 4) is an unprocessed pseudogene in the human genome that shares sequence similarity with the functional ferritin light chain (FTL) protein-coding gene. Unlike FTL, FTLP4 does not produce a protein and has no characterized biological, disease, or pharmacological functions. This pseudogene may be annotated in genomic databases due to sequence resemblance but is not a subject for therapeutic intervention. Diseases such as neuroferritinopathy or hyperferritinemia-cataract syndrome are associated with the functional FTL gene, not FTLP4.
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