Create issue ticket

6 Possible Causes for Mutation in the ETV Gene

  • Autosomal Dominant Thrombocytopenia 5

    Citation APA Style AAA Style APA Style Cell Style Chicago Style Harvard Style IEEE Style MLA Style Nature Style Vancouver Style BibTex Format Endnote Format RIS Format CSL Format DOIs only Format Pippucci, T, Savoia, A, Perrotta, S, Pujol-Moix, N, Noris, P, Castegnaro, G, […] Balduini, C.L. (2011). Mutations in the 5′ UTR[…][repub.eur.nl]

  • Acquired Sideroblastic Anemia

    In addition, the patients harboring germ line mutations in RUNX1, DDX41, ETV6, GATA2, ANKRD26, SRP72, CEBPA, and DDX41 genes have been found to have a higher genetic susceptibility[omicsonline.org] Five of the 8 genes (RUNX1, ETV-6, GATA2, CEBPA and DDX41 are related to “myeloid neoplasms with germline predisposition”, a new category of precursor myeloid disorder listed[omicsonline.org]

  • Oligodendroglioma of the Brain

    ETV/Pea3 family transcription factor-encoding genes are overexpressed in CIC -mutant oligodendrogliomas . Genes Chromosom. Cancer 54 , 725–733 (2015) 28. Liu, C. et al.[nature.com] Mutations in CIC and FUBP1 contribute to human oligodendroglioma . Science 333 , 1453–1455 (2011) 27. Padul, V. , Epari, S. , Moiyadi, A. , Shetty, P. & Shirsat, N. V.[nature.com]

  • X-Linked Sideroblastic Anemia and Ataxia

    In addition, the patients harboring germ line mutations in RUNX1, DDX41, ETV6, GATA2, ANKRD26, SRP72, CEBPA, and DDX41 genes have been found to have a higher genetic susceptibility[omicsonline.org] Five of the 8 genes (RUNX1, ETV-6, GATA2, CEBPA and DDX41 are related to “myeloid neoplasms with germline predisposition”, a new category of precursor myeloid disorder listed[omicsonline.org]

  • Autosomal Recessive Sideroblastic Anemia

    In addition, the patients harboring germ line mutations in RUNX1, DDX41, ETV6, GATA2, ANKRD26, SRP72, CEBPA, and DDX41 genes have been found to have a higher genetic susceptibility[omicsonline.org] Five of the 8 genes (RUNX1, ETV-6, GATA2, CEBPA and DDX41 are related to “myeloid neoplasms with germline predisposition”, a new category of precursor myeloid disorder listed[omicsonline.org]

  • Pancytopenia - Developmental Delay Syndrome

    In addition, the patients harboring germ line mutations in RUNX1, DDX41, ETV6, GATA2, ANKRD26, SRP72, CEBPA, and DDX41 genes have been found to have a higher genetic susceptibility[omicsonline.org] Five of the 8 genes (RUNX1, ETV-6, GATA2, CEBPA and DDX41 are related to “myeloid neoplasms with germline predisposition”, a new category of precursor myeloid disorder listed[omicsonline.org]

Further symptoms