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Disease Info Card
Npm1 Gene Mutation
Information about Npm1 Gene 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 Npm1 Gene Mutation
Most recent studies have shown that Npm1 Gene Mutation shares some biological mechanisms with acute-myeloid-leukemia-with-mutated-npm1, acute-promyelocytic-leukemia, adult-acute-myeloblastic-leukemia, cebpa-gene-mutation, cell-transformation-neoplastic, childhood-acute-myeloid-leukemia, cytogenetic-abnormality, dysmyelopoietic-syndromes, flt3-internal-tandem-duplication, hematologic-neoplasms, leukemia, leukemia-myelocytic-acute, leukemogenesis, malignant-neoplasms, mutation-abnormality, myeloid-leukemia, myeloid-leukemia-chronic, neoplasm-residual, neoplasms.
Among the many pathways, these few ones have gauged particular interests from scientists studying Npm1 Gene Mutation, and have been seen in publications frequently: Cell Cycle, Cell Death, Cell Growth, Cell Migration, Cell Proliferation, Centrosome Duplication, Demethylation, Dna Demethylation, Dna Hypermethylation, Dna Methylation, Hemopoiesis, Localization, Methylation, Nuclear Export, Pathogenesis, Regulation Of Cell Proliferation, Reverse Transcription, Ribosome Biogenesis
Quite a number of genes have been found to play important roles in Npm1 Gene Mutation, such as ABL1, ASXL1, CD34, CEBPA, EFS, FANCB, FLT3, IDH1, IDH2, INVS, KIT, LMLN, MID1, NPM1, RUNX1, SF3B1, TP53, WT1, YWHAE. 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.