Overview

Gene Location [1]
Xq25
Pathway
DNA damage/repair
Gene
STAG2

STAG2 Mutation is present in 2.29% of AACR GENIE cases, with non-small cell lung carcinoma, bladder carcinoma, malignant glioma, colorectal adenocarcinoma, and uterine corpus neoplasm having the greatest prevalence [4].

Top Disease Cases with STAG2 Mutation

Significance of STAG2 Mutation in Diseases

Malignant Solid Tumor +

Prostate Adenocarcinoma +

Breast Carcinoma +

Ovarian Carcinoma +

Colorectal Carcinoma +

Prostate Carcinoma +

Non-Hodgkin Lymphoma +

Cervical Carcinoma +

Small Cell Lung Carcinoma +

Non-Small Cell Lung Carcinoma +

Gastric Carcinoma +

Adenocarcinoma Of The Gastroesophageal Junction +

Cholangiocarcinoma +

Pancreatic Carcinoma +

Bladder Carcinoma +

Urothelial Carcinoma +

Myelodysplastic Syndromes +

Chronic Myelomonocytic Leukemia +

Penile Carcinoma +

Acute Myeloid Leukemia +

Endometrial Carcinoma +

Glioblastoma +

Squamous Cell Lung Carcinoma +

Melanoma +

Anal Carcinoma +

Lung Adenocarcinoma +

Head And Neck Carcinoma +

High Grade Ovarian Serous Adenocarcinoma +

Diffuse Large B-Cell Lymphoma +

Anaplastic Astrocytoma +

Head And Neck Squamous Cell Carcinoma +

Sarcoma +

Lymphoma +

Clear Cell Renal Cell Carcinoma +

Mesothelioma +

Pancreatic Adenocarcinoma +

Soft Tissue Sarcoma +

Fallopian Tube Carcinoma +

Histiocytic And Dendritic Cell Neoplasm +

Mantle Cell Lymphoma +

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

Myelodysplastic/Myeloproliferative Neoplasm, Unclassifiable +

Peritoneal Carcinoma +

Uveal Melanoma +

Vaginal Carcinoma +

Vulvar Carcinoma +

References

1. Hart R and Prlic A. Universal Transcript Archive Repository. Version uta_20170629. 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 4. 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.