Drug pipeline
Full profile accessExplore the programs pursuing this target and their development progress.
- Drug candidates
- Developers
- Development stage
Target intelligence / Profile preview
VWFP1 is a nonfunctional pseudogene located on chromosome 22 that duplicates the middle portion of the von Willebrand factor gene, spanning exons 23 to 34[1][2][3]. It is highly homologous (~97%) to the corresponding region of the VWF gene but does not encode a protein and is considered an evolutionary remnant. The existence of VWFP1 can complicate genetic analysis of VWF and von Willebrand disease due to gene conversion events, where sequences from VWFP1 may be introduced into the functional VWF gene, potentially contributing to genetic variation in VWF[1][3][4].
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 von Willebrand factor pseudogene 1 (VWFP1).