Biomarkers /
SRY
Overview
SRY is altered in 0.10% of all cancers with melanoma, lung adenocarcinoma, clear cell renal cell carcinoma, colon adenocarcinoma, and gastrointestinal neuroendocrine tumors having the greatest prevalence of alterations [3].
The most common alterations in SRY are SRY C36R (0.04%), SRY M100fs (0.02%), SRY M8V (0.02%), SRY P63L (0.02%), and SRY R75S (0.02%) [3].
Clinical Trials
Significance of SRY in Diseases
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. 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.
4. All assertions and clinical trial landscape data are curated from primary sources. You can read more about the curation process here.