Diseases /
Mixed Glioma
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Associated Genetic Biomarkers
Overview
NCI Definition: A tumor composed of two or more glial cell types (astrocytes, ependymal cells, and oligodendrocytes). [1]
Mixed gliomas most frequently harbor alterations in IDH1, TP53, ATRX, TERT, and NOTCH1 [2].
IDH1 Mutation, IDH1 Codon 132 Missense, IDH1 R132H, TP53 Mutation, and TP53 c.217-c.1178 Missense are the most common alterations in mixed glioma [2].
Clinical Trials
Significant Genes in Mixed Glioma
Disease Details
References
1. National Cancer Institute. NCI Thesaurus Version 18.11d. https://ncit.nci.nih.gov/ncitbrowser/ [2018-08-28]. [2018-09-21].
2. The AACR Project GENIE Consortium. AACR Project GENIE: powering precision medicine through an international consortium. Cancer Discovery. 2017;7(8):818-831. Dataset Version 8. This dataset does not represent the totality of the genetic landscape; see paper for more information.
3. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.