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Disease Info Card
Enzymopathy
Information about Enzymopathy: 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 Enzymopathy
Most recent studies have shown that Enzymopathy shares some biological mechanisms with anemia, anemia-hemolytic, anemia-hemolytic-congenital, anemia-hemolytic-congenital-nonspherocytic, celiac-disease, chronic-non-spherocytic-hemolytic-anemia, diabetes-mellitus, glucosephosphate-dehydrogenase-deficiency, hemolysis-(disorder), hemolytic-crisis, hyperbilirubinemia, icterus, inborn-errors-of-metabolism, infective-disorder, malaria, malnutrition, metabolic-diseases, neonatal-jaundice.
Among the many pathways, these few ones have gauged particular interests from scientists studying Enzymopathy, and have been seen in publications frequently: Adenine Salvage, Cellular Respiration, Cholesterol Esterification, Conjugation, Drug Resistance, Endocytosis, Excretion, Fatty Acid Oxidation, Flight, Gene Conversion, Glycolysis, Lipid Digestion, Localization, Pathogenesis, Protein Transport, Secretion, Translation, Transport, Urea Cycle, Xanthine Oxidation
Quite a number of genes have been found to play important roles in Enzymopathy, such as A4GALT, APRT, BPGM, CAT, G6PD, GLB1, GPI, HK1, INS, NT5E, PGD, QPCT, SMPD1, TPI1, UBL4A, XDH. 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.