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HADHA pseudogene 1 (HADHAP1) is classified as a pseudogene found in the human genome on chromosome 4. It is a non-functional copy of the HADHA gene, which codes for the alpha subunit of the mitochondrial trifunctional protein involved in fatty acid β-oxidation[2][4][7][8]. Unlike its parent gene, HADHA, HADHAP1 does not encode a functional protein and is not implicated as a molecular target in therapeutic or diagnostic applications. Some databases and literature may list aliases or alternative names that conflate this pseudogene with the functional HADHA gene or its protein products, but HADHAP1 itself is silent and does not play an active biological or disease-related role.
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