Overview

Gene Location [1]
4q31.3
Gene
FBXW7

FBXW7 Mutation is present in 2.94% of AACR GENIE cases, with colon adenocarcinoma, rectal adenocarcinoma, endometrial endometrioid adenocarcinoma, colorectal adenocarcinoma, and lung adenocarcinoma having the greatest prevalence [4].

Top Disease Cases with FBXW7 Mutation

Significance of FBXW7 Mutation in Diseases

Malignant Solid Tumor +

Breast Carcinoma +

Colon Carcinoma +

B-Cell Non-Hodgkin Lymphoma +

Lymphoma +

Cholangiocarcinoma +

Soft Tissue Sarcoma +

Osteosarcoma +

Gastrointestinal Stromal Tumor +

Leiomyosarcoma +

Acute Myeloid Leukemia +

Myeloid Neoplasm +

Multiple Myeloma +

Myelodysplastic Syndrome With Excess Blasts-2 +

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.