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Disease Info Card
Alpha-mannosidosis
Information about Alpha-mannosidosis: 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 Alpha-mannosidosis
Most recent studies have shown that Alpha-mannosidosis shares some biological mechanisms with ataxia, beta-mannosidosis, cat-diseases, cattle-diseases, dysostoses, fucosidase-deficiency-disease, gangliosidoses, glycogen-storage-disease-type-ii, goat-diseases, inborn-errors-of-metabolism, infective-disorder, lysosomal-storage-diseases, mannosidase-deficiency-diseases, metabolic-diseases, mucolipidoses, mucopolysaccharidoses, nervousness, pfaundler-hurler-syndrome, storage-disease.
Among the many pathways, these few ones have gauged particular interests from scientists studying Alpha-mannosidosis, and have been seen in publications frequently: Brain Development, Cell Adhesion, Embryo Development, Excretion, Glycosylation, Immune Response, Innate Immune Response, Intracellular Transport, Localization, Mating, Methylation, Myelination, Pathogenesis, Phagocytosis, Protein Glycosylation, Proteolysis, Secretion, System Development, Transport, Virulence
Quite a number of genes have been found to play important roles in Alpha-mannosidosis, such as ARHGAP4, CAT, CRAT, GLB1, GLYAT, GUCY2D, HNRNPC, MAG, MAN2A1, MAN2B1, MANBA, MBL2, MBP, MTSS1, NAGA, PFDN4, PTHLH, QPCT, SGSH. 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.