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PIP5K1B

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

PIP5K1B
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Phosphatidylinositol-4-phosphate 5-kinase type-1 beta is an enzyme that in humans is encoded by the PIP5K1B gene.[5][6][7]

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Abnormal silencing of the PIP5K1B gene contributes to the cytoskeletal defects seen in Friedreich's ataxia.[8]

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