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Disease Info Card
Glucagon Deficiency
Information about Glucagon Deficiency: 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 Glucagon Deficiency
Most recent studies have shown that Glucagon Deficiency shares some biological mechanisms with calcinosis, diabetes-mellitus, diabetes-mellitus-experimental, diabetes-mellitus-insulin-dependent, diabetes-mellitus-non-insulin-dependent, hyperglucagonaemia, hyperglycemia, hyperinsulinism, hypoglycemia, impaired-glucose-tolerance, insulin-resistance, insulin-sensitivity, ketosis, neonatal-hypoglycemia, obesity, pancreatic-diseases, pancreatitis, pancreatitis-chronic.
Among the many pathways, these few ones have gauged particular interests from scientists studying Glucagon Deficiency, and have been seen in publications frequently: Catecholamine Secretion, Cell Differentiation, Epinephrine Secretion, Excretion, Fibrinolysis, Glomerular Filtration, Glucagon Secretion, Gluconeogenesis, Glucose Homeostasis, Growth Hormone Secretion, Hormone Secretion, Induction Of Apoptosis, Insulin Secretion, Pancreas Development, Pathogenesis, Peptide Hormone Processing, Reflex, Response To Stress, Secretion, Urea Cycle
Quite a number of genes have been found to play important roles in Glucagon Deficiency, such as ARX, CBX4, ERMAP, FUT2, GCG, GCGR, INS, PCSK2, PEX7, PHYH, POMC, PPY, SQLE, SST, UBA2. 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.