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Disease Info Card
Peroxisomal Disorders
Information about Peroxisomal Disorders: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Peroxisomal Disorders
Most recent studies have shown that Peroxisomal Disorders shares some biological mechanisms with acidemia, adrenoleukodystrophy, adrenoleukodystrophy-neonatal, adrenomyeloneuropathy, chondrodysplasia-punctata, chondrodysplasia-punctata-rhizomelic, demyelination, disorders-of-peroxisome-biogenesis, inborn-errors-of-metabolism, infantile-refsum-disease-(disorder), metabolic-diseases, muscle-hypotonia, nervous-system-disorder, nervousness, protein-deficiency, refsum-disease, zellweger-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Peroxisomal Disorders, and have been seen in publications frequently: Aging, Brain Development, Cell Death, Excretion, Fatty Acid Alpha-oxidation, Fatty Acid Beta-oxidation, Fatty Acid Oxidation, Lipid Storage, Localization, Membrane Assembly, Myelination, Oxidative Phosphorylation, Pathogenesis, Pigmentation, Protein Import, Secretion, Spermatogenesis, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Peroxisomal Disorders, such as ABCD1, ABCD2, ABCD3, ACOX1, AMACR, CAT, GNPAT, HSD17B4, PEX1, PEX10, PEX13, PEX2, PEX5, PEX6, PEX7, PHEX, PHYH, ZNF260. 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 disease. Plesae stay updated.