PEX14 deficiency (Q97740): Difference between revisions

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15 August 2026
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Latest revision as of 13:52, 16 August 2026

This refers to the deficiency in the protein that in humans is encoded by the PEX14 gene. This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal.
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ID_1699637272
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    PEX14 deficiency
    This refers to the deficiency in the protein that in humans is encoded by the PEX14 gene. This gene encodes an essential component of the peroxisomal import machinery. The protein is integrated into peroxisome membranes with its C-terminus exposed to the cytosol, and interacts with the cytosolic receptor for proteins containing a PTS1 peroxisomal targeting signal.

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      CID11:ID_1699637272
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      dki-india-ID_1699637272
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      Concluído
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      15 August 2026
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