Biomarkers /
RARA
Overview
RARA (Retinoic acid receptor, alpha) is a gene that encodes for a nuclear retinoic acid receptor, a transcription regulating protein (Gene 2013b). In cancer, rearrangements involving RARA have been observed in AML and APL. Its role is also being investigated in gastric and other cancers.
RARA is altered in 1.69% of all cancers with breast invasive ductal carcinoma, lung adenocarcinoma, colon adenocarcinoma, esophageal adenocarcinoma, and invasive breast carcinoma having the greatest prevalence of alterations [3].
The most common alterations in RARA are RARA Amplification (0.75%), RARA Fusion (0.11%), RARA Loss (0.05%), RARA P441fs (0.03%), and RARA R394Q (0.03%) [3].
Biomarker-Directed Therapies
Clinical Trials
Significance of RARA 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.