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Disease Info Card
De Novo Mutation
Information about De Novo Mutation: 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 De Novo Mutation
Most recent studies have shown that De Novo Mutation shares some biological mechanisms with anemia, atrophy, carcinoma, cardiomyopathies, complete-hearing-loss, congenital-abnormality, diabetes-mellitus, dysplasia, dystrophy, embryonic-mosaic, epilepsy, hereditary-diseases, malignant-neoplasms, muscular-dystrophy, myopathy, neoplasms, nervousness.
Among the many pathways, these few ones have gauged particular interests from scientists studying De Novo Mutation, and have been seen in publications frequently: Aging, Cell Proliferation, Coagulation, Dna Amplification, Drug Resistance, Excretion, Gene Conversion, Glycosylation, Insulin Secretion, Localization, Mating, Meiosis, Methylation, Oogenesis, Pathogenesis, Pigmentation, Secretion, Spermatogenesis, Translation, Transport
Quite a number of genes have been found to play important roles in De Novo Mutation, such as APC, AR, CFTR, CYP21A2, DMD, G6PD, GJB1, GJB2, HBB, INS, LDLR, LMNA, MPZ, OTC, PAH, PMP22, PRNP, VWF. 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.