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Pex3 - Peroxin 3

Predicted to enable protein-macromolecule adaptor activity. Involved in fatty acid elongation; peroxisome organization; and positive regulation of ceramide biosynthetic process. Located in endoplasmic reticulum and peroxisome. Is expressed in adult head; embryonic cortex; embryonic/larval midgut; and organism. Used to study Zellweger syndrome. Human ortholog(s) of this gene implicated in Peroxisome biogenesis disorder 10B and peroxisome biogenesis disorder 10A. Orthologous to human PEX3 (peroxisomal biogenesis factor 3). [provided by Alliance of Genome Resources, Dec 2024]

Genes similar to Pex3

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Species Gene Architecture aa