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HMGN1P17 is an intronless human pseudogene that structurally resembles the gene encoding high mobility group nucleosome binding domain 1 (HMGN1). Pseudogenes like HMGN1P17 commonly arise from gene duplication or reverse transcription events and accumulate mutations that prevent expression of a functional protein. These DNA segments may be transcribed at low levels but are generally considered nonfunctional “genetic fossils.” There is no evidence that HMGN1P17 encodes a protein or has a therapeutically relevant function.
None. Not applicable.
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