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Disease Info Card
Cystinuria
Information about Cystinuria: 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 Cystinuria
Most recent studies have shown that Cystinuria shares some biological mechanisms with aminoaciduria, cystinosis, hartnup-disease, hepatolenticular-degeneration, hereditary-diseases, homocystinuria, hypercalciuria, hyperoxaluria, inborn-errors-of-metabolism, kidney-calculi, kidney-diseases, lithiasis, metabolic-diseases, nephrolithiasis, phenylketonurias, renal-aminoacidurias, renal-tubular-acidosis, urinary-tract-infection, urolithiasis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cystinuria, and have been seen in publications frequently: Amino Acid Transport, Basic Amino Acid Transport, Cell Death, Cellular Homeostasis, Diuresis, Excretion, Glomerular Filtration, Intestinal Absorption, L-cystine Transport, Localization, Lysine Transport, Neutral Amino Acid Transport, Pathogenesis, Peptide Transport, Programmed Cell Death, Protein Digestion, Secretion, Transepithelial Transport, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Cystinuria, such as CP, CYCS, DDX39A, DIO2, HLA-DQA1, HLCS, INS, MPG, NOD2, PPM1B, PREP, PREPL, SLC3A1, SLC3A2, SLC7A5, SLC7A7, SLC7A9, XDH. 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.