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Disease Info Card
Medullary Cystic Disease
Information about Medullary Cystic 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 Medullary Cystic Disease
Most recent studies have shown that Medullary Cystic Disease shares some biological mechanisms with cystic-disease--retired-, cystic-kidney-diseases, familial-juvenile-gout, fibrosis, gout, hypertensive-disease, hyperuricaemic-nephropathy, hyperuricemia, kidney-diseases, kidney-failure, kidney-failure-chronic, medullary-cystic-kidney-disease-type-2, medullary-sponge-kidney, nephritis, nephritis-interstitial, nephronophthisis, nephronophthisis-familial-juvenile, polycystic-kidney-autosomal-dominant, polycystic-kidney-diseases.
Among the many pathways, these few ones have gauged particular interests from scientists studying Medullary Cystic Disease, and have been seen in publications frequently: Bone Resorption, Excretion, Glomerular Filtration, Glycosylation, Inflammatory Response, Ion Transport, Localization, Mitosis, Natriuresis, Pathogenesis, Protein Processing, Protein Transport, Regulation Of Blood Pressure, Renal Tubule Morphogenesis, Secretion, Secretory Pathway, Transport
Quite a number of genes have been found to play important roles in Medullary Cystic Disease, such as ALDH3A2, GLI2, HNF1B, INVS, KCNJ1, MLYCD, NPHP1, NPHP3, NPHP4, NPR1, NXPH1, PKD1, PKD2, PKHD1, PRKD1, RAPGEF5, REN, RHBG, UMOD. 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.