Cebpa Gene Mutation

Overview of Cebpa Gene Mutation

Most recent studies have shown that Cebpa Gene Mutation shares some biological mechanisms with acute-leukemia, acute-myeloid-leukemia-m1, adult-acute-myeloblastic-leukemia, chromosomal-translocation, clonal-evolution, cytogenetic-abnormality, endometrial-polyp, flt3-internal-tandem-duplication, leukemia, leukemia-myelocytic-acute, leukemogenesis, malignant-neoplasms, monosomy, mutation-out-of-frame, myeloid-leukemia, myeloid-neoplasm, myelomonocytic-leukemia, neoplasms, npm1-gene-mutation, secondary-acute-myeloid-leukemia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Cebpa Gene Mutation, and have been seen in publications frequently: Cell Differentiation, Cell Proliferation, Dna Hypermethylation, Granulocyte Differentiation, Methylation, Mitotic Recombination, Myeloid Cell Differentiation, Translation

Quite a number of genes have been found to play important roles in Cebpa Gene Mutation, such as ABL1, ANPEP, CCND3, CD33, CD34, CD7, CEBPA, FANCB, FLT3, INVS, KIT, LMLN, MID1, NPM1, RUNX1, SFRP1, SFRP5, UGP2. 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.

Cebpa Gene Mutation Related Genes

click to see detail information for each gene

Pathways Related to Cebpa Gene Mutation

This information is being compiled and will come in a future update

Related Diseases