Biomarkers /
PRKACA
Overview
PRKACA is altered in 0.13% of all cancers with fibrolamellar carcinoma, hepatocellular carcinoma, conventional glioblastoma multiforme, pancreatic adenocarcinoma, and adenocarcinoma of unknown primary having the greatest prevalence of alterations [3].
The most common alterations in PRKACA are PRKACA-DNAJB1 Fusion (0.03%), PRKACA A224V (0.09%), PRKACA A233V (0.07%), PRKACA A35T (0.07%), and PRKACA E108V (0.07%) [3].
Clinical Trials
Significance of PRKACA 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.