Associated Genetic Biomarkers

Overview

Gene Location [1]
21q22.12
Variant Type
Substitution - Nonsense
Affected Exon Number
4
Gene
RUNX1
Protein Domain [2]
Runt

RUNX1 R139* is present in 0.07% of AACR GENIE cases, with acute myeloid leukemia with myelodysplasia-related changes, acute myeloid leukemia, myelodysplastic syndromes, endometrial endometrioid adenocarcinoma, and B-cell lymphoblastic leukemia/lymphoma having the greatest prevalence [4].

Top Disease Cases with RUNX1 R139*

References

1. Hart R and Prlic A. Universal Transcript Archive Repository. Version uta_20180821. San Francisco CA: Github;2015. https://github.com/biocommons/uta

2. The UniProt Consortium. UniProt: a worldwide hub of protein knowledge. Nucleic Acids Research. 2019;47:D506-D515.

3. Liu X, Wu C, Li C, and Boerwinkle E. dbNSFP v3.0: A one-stop database of functional predictions and annotations for human nonsynonymous and splice site SNVs. Human Mutation. 2015;37:235-241.

Liu X, Jian X, and Boerwinkle E. dbNSFP: A lightweight database of human nonsynonymous SNPs and their functional predictions. Human Mutation. 2011;32:894-899.

4. 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.

5. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.