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Disease Info Card
Storage Disease
Information about Storage 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 Storage Disease
Most recent studies have shown that Storage Disease shares some biological mechanisms with cardiomyopathies, cholesterol-ester-storage-disease, fabry-disease, gaucher-disease, glycogen-storage-disease, glycogen-storage-disease-type-i, glycogen-storage-disease-type-ii, glycogen-storage-disease-type-iii, hepatomegaly, hypertrophy, hypoglycemia, inborn-errors-of-metabolism, lipoidosis, liver-diseases, lysosomal-storage-diseases, metabolic-diseases, mucopolysaccharidoses, myopathy, nervousness, niemann-pick-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Storage Disease, and have been seen in publications frequently: Autophagy, Cell Death, Cholesterol Storage, Endocytosis, Excretion, Fatty Acid Oxidation, Glomerular Filtration, Gluconeogenesis, Glucose Homeostasis, Glucose-6-phosphate Transport, Glycolysis, Glycosylation, Immune Response, Lipid Storage, Localization, Pathogenesis, Secretion, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Storage Disease, such as AGA, AGL, ARSA, ARSB, ATP8A2, CSF3, G6PC, GAA, GBA, GBE1, GLA, GLB1, GUSB, LIPA, NPC1, PNPLA2, SLC17A5, SLC37A4. 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.