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Disease Info Card
Glucosephosphate Dehydrogenase Deficiency
Information about Glucosephosphate Dehydrogenase 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 Glucosephosphate Dehydrogenase Deficiency
Most recent studies have shown that Glucosephosphate Dehydrogenase Deficiency shares some biological mechanisms with anemia, anemia-hemolytic, anemia-hemolytic-congenital, anemia-hemolytic-congenital-nonspherocytic, anemia-sickle-cell, beta-thalassemia, hemoglobinopathies, hemolysis-(disorder), hyperbilirubinemia, icterus, inborn-errors-of-metabolism, kernicterus, malaria, malaria-falciparum, methemoglobinemia, neonatal-jaundice, sickle-cell-trait, thalassemia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Glucosephosphate Dehydrogenase Deficiency, and have been seen in publications frequently: Aging, Bilirubin Conjugation, Blood Coagulation, Cell Death, Cell Growth, Cell Proliferation, Chemotaxis, Coagulation, Conjugation, Drug Resistance, Excretion, Glycolysis, Hypersensitivity, Pathogenesis, Phagocytosis, Regeneration, Respiratory Burst, Secretion, Senescence, Transport
Quite a number of genes have been found to play important roles in Glucosephosphate Dehydrogenase Deficiency, such as A4GALT, ABO, ADA, CAT, G6PC, G6PD, GPI, GSR, HBG2, HP, PGD, TF, TNF, TPI1, UBL4A, UGT1A1. 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.