Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
TMX2-CTNND1 readthrough is a naturally occurring transcript resulting from transcriptional readthrough between the adjacent TMX2 and CTNND1 genes on chromosome 11[3][2][9][4]. This transcript is classified as a candidate for nonsense-mediated decay and, unlike its parental protein-coding genes, does not typically produce a protein. Pathological fusion events involving this locus can disrupt normal cellular function, leading to aberrancies in cell adhesion and signaling pathways that may contribute to oncogenesis[1][5]. However, as a ncRNA, TMX2-CTNND1 itself is neither a receptor nor an enzyme, and is not considered a therapeutic target.
Not applicable for the readthrough itself. For pathological fusions (if expressed as protein): Disruption of cell adhesion, signaling, and transcriptional regulation.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Explore the programs pursuing this target and their development progress.
Follow the clinical studies evaluating therapies directed at this target.
Compare approaches across drug candidates, modalities, and indications.
Investigate the research and source evidence behind target biology and development.
Explore patent activity around therapies and technologies addressing this target.
Connect target biology, drug development, and emerging evidence in your research.
See how Gosset can support your research on TMX2-CTNND1 readthrough (nonsense-mediated decay candidate) (TMX2-CTNND1).