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Disease Info Card
Chromosomal Deletion
Information about Chromosomal Deletion: 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 Chromosomal Deletion
Most recent studies have shown that Chromosomal Deletion shares some biological mechanisms with aneuploidy, chromosomal-translocation, congenital-abnormality, congenital-heart-defects, cytogenetic-abnormality, developmental-delay-(disorder), growth-retardation, hypoplasia, leukemia, malignant-neoplasms, microcephaly, monosomy, neoplasms, partial-trisomy, trisomy, unbalanced-translocation.
Among the many pathways, these few ones have gauged particular interests from scientists studying Chromosomal Deletion, and have been seen in publications frequently: Cell Cycle, Cell Death, Cell Growth, Dna Methylation, Fertilization, Hypersensitivity, Interphase, Localization, Mating, Meiosis, Metaphase, Methylation, Nitrogen Fixation, Pathogenesis, Pigmentation, Secretion, Translation, Transport, Transposition, Virulence
Quite a number of genes have been found to play important roles in Chromosomal Deletion, such as CDK5R1, CDKN2B, CHP1, ENDOU, EXOSC6, INVS, LMLN, MB, NXT1, PAFAH1B1, PTER, PTGES3, RRAS, S100A10, SUB1, TBX1, TMED10, TP53, TPPP. 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.