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Human INPPL1 wild-type allele is located in the vicinity of 11q13.4 and is approximately 15 kb in length. This allele, which encodes phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 protein, is involved in the regulation of PI3K-dependent insulin signaling. Mutations in the gene are associated with opsismodysplasia.
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