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Disease Info Card
Congenital Disorders Of Glycosylation
Information about Congenital Disorders Of Glycosylation: 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 Congenital Disorders Of Glycosylation
Most recent studies have shown that Congenital Disorders Of Glycosylation shares some biological mechanisms with ataxia, atrophy, blood-coagulation-disorders, carbohydrate-deficient-glycoprotein-syndrome-type-i, congenital-cerebellar-hypoplasia, congenital-disorders, developmental-delay-(disorder), failure-to-thrive, hypoglycemia, hypoplasia, inborn-errors-of-metabolism, intestinal-diseases, liver-diseases, metabolic-diseases, muscle-hypotonia, nervousness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Congenital Disorders Of Glycosylation, and have been seen in publications frequently: Blood Coagulation, Brain Development, Cell Adhesion, Coagulation, Cytolysis, Fucosylation, Glycosylation, Hemostasis, Immune Response, Insulin Secretion, Intracellular Transport, Lipid Glycosylation, Localization, Pathogenesis, Protein Folding, Protein Glycosylation, Secretion, Secretory Pathway, Translation, Transport
Quite a number of genes have been found to play important roles in Congenital Disorders Of Glycosylation, such as ALG1, ALG6, APOC3, COG1, COG7, DAG1, DPM1, HP, MGAT2, MPI, PMM1, PMM2, SERPINC1, SLPI, TF, TMEM11. 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.