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Disease Info Card
Nephronophthisis
Information about Nephronophthisis: 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 Nephronophthisis
Most recent studies have shown that Nephronophthisis shares some biological mechanisms with cystic-disease--retired-, cystic-kidney-diseases, dysplasia, familial-aplasia-of-the-vermis, fibrosis, hepatic-fibrosis, hydrocephalus-normal-pressure, kidney-diseases, kidney-failure, kidney-failure-chronic, medullary-cystic-disease, nephritis, nephritis-interstitial, nephronophthisis-familial-juvenile, polycystic-kidney-autosomal-dominant, polycystic-kidney-diseases, polyuria, retinal-degeneration, retinitis-pigmentosa.
Among the many pathways, these few ones have gauged particular interests from scientists studying Nephronophthisis, and have been seen in publications frequently: Cell Adhesion, Cell Cycle, Cell Death, Cell Division, Cell Proliferation, Central Nervous System Development, Convergent Extension, Excretion, Glomerular Filtration, Intraflagellar Transport, Localization, Mating, Mitosis, Neural Tube Closure, Pathogenesis, Pronephros Development, Pronephros Morphogenesis, Secretion, Transport, Tube Closure
Quite a number of genes have been found to play important roles in Nephronophthisis, such as AHI1, ALDH3A2, CEP290, INVS, IQCB1, MKKS, MKS1, NEK8, NPHP1, NPHP3, NPHP4, NXPH1, PKD1, PKD2, PKHD1, PRKD1, RPGRIP1L, TMEM67, 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.