This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Mannosidase Deficiency Diseases
Information about Mannosidase Deficiency Diseases: 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 Mannosidase Deficiency Diseases
Most recent studies have shown that Mannosidase Deficiency Diseases shares some biological mechanisms with alpha-mannosidosis, aspartylglucosaminuria, ataxia, cat-diseases, cattle-diseases, dysostoses, fabry-disease, fucosidase-deficiency-disease, gangliosidoses, inborn-errors-of-metabolism, infective-disorder, lysosomal-storage-diseases, mucolipidoses, mucopolysaccharidoses, nervous-system-disorder, nervousness, pfaundler-hurler-syndrome, storage-disease, type-ii-mucolipidosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mannosidase Deficiency Diseases, and have been seen in publications frequently: Autolysis, Carbohydrate Storage, Catabolic Process, Cell Differentiation, Endocytosis, Excretion, Glycosylation, Immunoglobulin Production, Intracellular Transport, Lipid Storage, Localization, Locomotion, Methylation, Myelination, Pathogenesis, Phagocytosis, Proteolysis, Secretion, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Mannosidase Deficiency Diseases, such as ARSA, ARSB, CAT, CP, CRAT, GLB1, GLYAT, GPI, GUSB, MAN2B1, MAN2C1, MANBA, MAOA, MID1, PGR, PLEKHM1, QPCT. 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.