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Disease Info Card
Dent's Disease
Information about Dent's 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 Dent's Disease
Most recent studies have shown that Dent's Disease shares some biological mechanisms with acidosis, aminoaciduria, bartter-disease, fanconi-syndrome, fibrosis, genetic-diseases-x-linked, hypercalciuria, hypophosphatemia, hypophosphatemic-rickets, kidney-calculi, kidney-diseases, kidney-failure, kidney-failure-chronic, nephrocalcinosis, nephrolithiasis, oculocerebrorenal-syndrome, proteinuria-of-undiagnosed-cause, renal-tubular-acidosis, renal-tubular-disorder, rickets.
Among the many pathways, these few ones have gauged particular interests from scientists studying Dent's Disease, and have been seen in publications frequently: Amino Acid Transport, Chloride Transport, Endocytosis, Excretion, Glomerular Filtration, Glycosylation, Intestinal Absorption, Localization, Micropinocytosis, Pathogenesis, Proteolysis, Proton Transport, Receptor-mediated Endocytosis, Regeneration, Reverse Transcription, Secretion, Transcytosis, Transepithelial Transport, Translation, Transport
Quite a number of genes have been found to play important roles in Dent's Disease, such as ALB, CFTR, CLC, CLCF1, CLCN1, CLCN3, CLCN4, CLCN5, CLCN7, CLCNKB, CUBN, INPP5B, KCNJ1, LRP2, OCRL, PTH, RAB5A, SLC12A1, SLC12A3. 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.