| ID | Sequence | Length | GC content |
|---|---|---|---|
| AGUUCUAACCUGCUCUGCAGGAAUAACGGUCCUGCCUCCCGACACUCUU… | 9193 nt | 0.3890 | |
| AGUUCUAACCUGCUCUGCAGGAAUAACGGUCCUGCCUCCCGACACUCUU… | 9265 nt | 0.3895 |
The protein encoded by this gene is a member of the Zfh1 family of 2-handed zinc finger/homeodomain proteins. It is located in the nucleus and functions as a DNA-binding transcriptional repressor that interacts with activated SMADs. Mutations in this gene are associated with Hirschsprung disease/Mowat-Wilson syndrome. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Jan 2010]
A study in mice demonstrated that the ZEB2 is upregulated in stressed cardiomyocytes, where it induces cardioprotective cross-talk between cardiomyocytes and endothelial cells and enhances post-ischemic angiogenesis [Li et al. DOI:10.3389/fcvm.2022.768834]. Further research in mouse models confirmed that the ZEB2 functions as a mediator of cardiomyocyte-endothelial cell interaction, inducing cardiomyocytes to produce TMSB4 and PTMA, which drive endothelial cell migration and proliferation [Bian et al. DOI:10.3892/mmr.2025.13680].