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  • Human ASXL1 wild-type allele is located in the vicinity of 20q11 and is approximately 81 kb in length. This allele, which encodes putative Polycomb group protein ASXL1, may play a role in the regulation of both chromatin structure and transcription. Mutation of the gene is associated with both myelodysplastic syndromes and chronic myelomonocytic leukemia.
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