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Peroxisomal biogenesis factor 2

Index Peroxisomal biogenesis factor 2

Peroxisomal biogenesis factor 2 is a protein that in humans is encoded by the PEX2 gene. [1]

4 relations: Gene, Infantile Refsum disease, Protein, Zellweger syndrome.

Gene

In biology, a gene is a sequence of DNA or RNA that codes for a molecule that has a function.

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Infantile Refsum disease

Infantile Refsum disease (IRD), also called infantile phytanic acid storage disease, is a rare autosomal recessive congenital peroxisomal biogenesis disorder within the Zellweger spectrum.

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Protein

Proteins are large biomolecules, or macromolecules, consisting of one or more long chains of amino acid residues.

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Zellweger syndrome

Zellweger syndrome, also called cerebrohepatorenal syndrome, is a rare congenital disorder characterized by the reduction or absence of functional peroxisomes in the cells of an individual.

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Redirects here:

PEX2, PEX2 (gene), PXMP3.

References

[1] https://en.wikipedia.org/wiki/Peroxisomal_biogenesis_factor_2

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