This website uses cookies to ensure you get the best experience on our website.
- Table of Contents
, No Gclids
Disease Info Card
Carbamoyl-phosphate Synthase I Deficiency Disease
Information about Carbamoyl-phosphate Synthase I Deficiency 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 Carbamoyl-phosphate Synthase I Deficiency Disease
Most recent studies have shown that Carbamoyl-phosphate Synthase I Deficiency Disease shares some biological mechanisms with argininosuccinic-aciduria, cerebral-edema, citrullinemia, comatose, diabetes-mellitus, edema, hyperammonemia, hyperargininemia, inborn-errors-of-metabolism, liver-carcinoma, liver-neoplasms-experimental, maple-syrup-urine-disease, metabolic-diseases, ornithine-carbamoyltransferase-deficiency, reye-syndrome, steatosis, urea-cycle-disorders-inborn, vomiting.
Among the many pathways, these few ones have gauged particular interests from scientists studying Carbamoyl-phosphate Synthase I Deficiency Disease, and have been seen in publications frequently: Cell Cycle, Dna Repair, Excretion, Fermentation, Gluconeogenesis, Habituation, Lactation, Liver Development, Localization, Macroautophagy, Protein Folding, Proteolysis, Regulation Of Proteolysis, S Phase, Senescence, Translation, Transport, Urea Cycle, Wound Healing
Quite a number of genes have been found to play important roles in Carbamoyl-phosphate Synthase I Deficiency Disease, such as ALB, ASL, ASS1, CAD, CPS1, CYP21A2, G6PC, GCK, GLS, INS, NAGS, OAT, OTC, PM20D1, QPCT, SP1. 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.