Peroxisome Degradation

Overview of Peroxisome Degradation

Most recent studies have shown that Peroxisome Degradation shares some biological mechanisms with autophagy, catabolic-process, cvt-pathway, developmental-process, endocytosis, glucose-transport, localization, macroautophagy, macropexophagy, meiosis, organelle-assembly, pathogenesis, protein-import, protein-targeting, proteolysis, response-to-nutrient, sporulation, transport.

Among the many pathways, these few ones have gauged particular interests from scientists studying Peroxisome Degradation, and have been seen in publications frequently: autophagy, catabolic-process, cvt-pathway, developmental-process, endocytosis, glucose-transport, localization, macroautophagy, macropexophagy, meiosis, organelle-assembly, pathogenesis, protein-import, protein-targeting, proteolysis, response-to-nutrient, sporulation, transport

Quite a number of genes have been found to play important roles in Peroxisome Degradation, such as ACSL6, ACSS2, ALOX15, ATG7, CAT, DAO, GABARAPL1, GABARAPL2, GDF5, GTF2H1, Lxn, PAG1, PEX11A, PEX14, PEX3, PHEX, PRDX1, TGM2, ULK1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this pathway. Plesae stay updated.

Peroxisome Degradation Related Genes

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Diseases Related to Peroxisome Degradation

This information is being compiled and will come in a future update

Related pathways