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Disease Info Card
Ornithine Carbamoyltransferase Deficiency
Information about Ornithine Carbamoyltransferase Deficiency: 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 Ornithine Carbamoyltransferase Deficiency
Most recent studies have shown that Ornithine Carbamoyltransferase Deficiency shares some biological mechanisms with argininosuccinic-aciduria, citrullinemia, comatose, edema, encephalopathies, hyperammonaemic-encephalopathy, hyperammonemia, hyperargininemia, inborn-errors-of-metabolism, lethargy, liver-diseases, metabolic-diseases, orotic-aciduria, reye-syndrome, urea-cycle-disorders-inborn, vomiting.
Among the many pathways, these few ones have gauged particular interests from scientists studying Ornithine Carbamoyltransferase Deficiency, and have been seen in publications frequently: Cell Adhesion, Coagulation, Conjugation, Excretion, Fatty Acid Oxidation, Fertilization, Immune Response, Inflammatory Response, Localization, Mrna Splicing, Myelination, Ornithine Transport, Pathogenesis, Protein Acetylation, Regeneration, Rna Splicing, Secretion, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Ornithine Carbamoyltransferase Deficiency, such as ABCB11, ADSL, ARSH, ASL, ASS1, CHAT, DMD, FBN1, GLUL, GRB2, NAGS, OTC, QPCT, RPGR, SEC14L2, 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.