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Disease Info Card
Uniparental Disomy
Information about Uniparental Disomy: 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 Uniparental Disomy
Most recent studies have shown that Uniparental Disomy shares some biological mechanisms with aneuploidy, angelman-syndrome, beckwith-wiedemann-syndrome, chromosomal-translocation, congenital-abnormality, cytogenetic-abnormality, dwarfism, embryonic-mosaic, fetal-growth-retardation, growth-disorders, growth-retardation, isodisomies-uniparental, leukemia, malignant-neoplasms, neoplasms, obesity, prader-willi-syndrome, russell-silver-syndrome, trisomy.
Among the many pathways, these few ones have gauged particular interests from scientists studying Uniparental Disomy, and have been seen in publications frequently: Brain Development, Cell Division, Cell Proliferation, Demethylation, Dna Methylation, Dna Replication, Fertilization, Genetic Imprinting, Interphase, Localization, Meiosis, Meiosis I, Meiosis Ii, Metaphase, Methylation, Mitosis, Mitotic Recombination, Pathogenesis, Pigmentation, Secretion
Quite a number of genes have been found to play important roles in Uniparental Disomy, such as ASXL1, CBL, CDKN1C, CDKN2A, DLK1, GABRB3, GRB10, IGF2, JAK2, LMLN, MEST, MKRN3, SMS, SNRPN, TP53, UBE3A, UROD. 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.