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Disease Info Card
Orotic Aciduria
Information about Orotic Aciduria: 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 Orotic Aciduria
Most recent studies have shown that Orotic Aciduria shares some biological mechanisms with anemia, anemia-macrocytic, citrullinemia, comatose, encephalopathies, growth-disorders, hereditary-diseases, hyperammonemia, hyperargininemia, immunologic-deficiency-syndromes, inborn-errors-of-metabolism, lysinuric-protein-intolerance, metabolic-diseases, ornithine-carbamoyltransferase-deficiency, urea-cycle-disorders-inborn, vomiting.
Among the many pathways, these few ones have gauged particular interests from scientists studying Orotic Aciduria, and have been seen in publications frequently: Aging, Amino Acid Transport, Cell Cycle, Coagulation, Dna Replication, Excretion, Fatty Acid Oxidation, Glomerular Filtration, Lactation, Localization, Mating, Ornithine Transport, Pathogenesis, Proteolysis, Regeneration, S Phase, Translation, Transport, Urea Cycle, Wound Healing
Quite a number of genes have been found to play important roles in Orotic Aciduria, such as ADA, APRT, ARSH, ASL, DHODH, DPYD, GRB2, HPRT1, OAT, ODC1, OTC, PNP, SEC14L2, SLC25A21, SLC7A7, TSHZ1, UMPS. 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.