Overview

Gene Location [1]
19p13.3
Gene
STK11

STK11 Mutation is present in 1.76% of AACR GENIE cases, with lung adenocarcinoma, breast invasive ductal carcinoma, colon adenocarcinoma, non-small cell lung carcinoma, and adenocarcinoma of unknown primary having the greatest prevalence [4].

Top Disease Cases with STK11 Mutation

Significance of STK11 Mutation in Diseases

Malignant Solid Tumor +

Prostate Adenocarcinoma +

Non-Small Cell Lung Carcinoma +

Prostate Carcinoma +

Breast Carcinoma +

Ovarian Carcinoma +

Colorectal Carcinoma +

Cervical Carcinoma +

Endometrial Carcinoma +

Non-Hodgkin Lymphoma +

Primary Peritoneal Carcinoma +

Fallopian Tube Carcinoma +

Cholangiocarcinoma +

Head And Neck Squamous Cell Carcinoma +

Adenocarcinoma Of The Gastroesophageal Junction +

Pancreatic Carcinoma +

Urothelial Carcinoma +

Lung Adenocarcinoma +

Anal Carcinoma +

Penile Carcinoma +

Cancer +

Mature T-Cell And NK-Cell Non-Hodgkin Lymphoma +

Squamous Cell Lung Carcinoma +

Malignant Small Intestinal Neoplasm +

Melanoma +

Gastric Carcinoma +

Malignant Gastric Neoplasm +

Malignant Esophagogastric Neoplasm +

Bladder Carcinoma +

Ampulla Of Vater Carcinoma +

Bladder Urothelial Carcinoma +

Pancreatic Adenocarcinoma +

Malignant Intestinal Neoplasm +

Histiocytic And Dendritic Cell Neoplasm +

Small Cell Lung Carcinoma +

Thyroid Gland Carcinoma +

Esophageal Carcinoma +

Mesothelioma +

Malignant Ovarian Epithelial Tumor +

Renal Cell Carcinoma +

Clear Cell Renal Cell Carcinoma +

Uveal Melanoma +

Multiple Myeloma +

Soft Tissue Sarcoma +

Diffuse Large B-Cell Lymphoma +

B-Cell Non-Hodgkin Lymphoma +

High Grade Ovarian Serous Adenocarcinoma +

Gastrointestinal Stromal Tumor +

Mantle Cell Lymphoma +

Vaginal Carcinoma +

Vulvar Carcinoma +

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.