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Disease Info Card
Gaucher Disease
Information about Gaucher Disease: 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 Gaucher Disease
Most recent studies have shown that Gaucher Disease shares some biological mechanisms with anemia, bone-diseases, fabry-disease, gaucher-disease-type-1, gaucher-disease-type-2-(disorder), hepatomegaly, hypersplenism, inborn-errors-of-metabolism, leukemia, lipoidosis, lysosomal-storage-diseases, metabolic-diseases, mucopolysaccharidoses, nervousness, niemann-pick-diseases, pain, parkinson-disease, sphingolipidoses, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Gaucher Disease, and have been seen in publications frequently: Autophagy, Bone Remodeling, Bone Resorption, Cell Death, Cell Proliferation, Coagulation, Endocytosis, Excretion, Gene Conversion, Glycosylation, Hypersensitivity, Lipid Storage, Localization, Macrophage Activation, Pathogenesis, Phagocytosis, Protein Folding, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Gaucher Disease, such as ACE, ARSA, CCL18, CTLA4, ELF3, GALC, GBA, GLB1, HLA-DQA1, IL6, MTCH1, NOD2, PAEP, PSAP, QPCT, SMPD1, SNCA, UGCG. 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.