# Zinc finger E-box binding homeobox 2

> mammalian protein found in Mus musculus

**Wikidata**: [Q15318497](https://www.wikidata.org/wiki/Q15318497)  
**Source**: https://4ort.xyz/entity/zinc-finger-e-box-binding-homeobox-2-q15318497


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q9R0G7)
3. Q20641742
4. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
5. [Smicl is a novel Smad interacting protein and cleavage and polyadenylation specificity factor associated protein](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
6. [Sip1 downstream Effector ninein controls neocortical axonal growth, ipsilateral branching, and microtubule growth and stability](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9R0G7&geneProductId=UniProtKB:Q9R0G7)
7. [Sip1 downstream Effector ninein controls neocortical axonal growth, ipsilateral branching, and microtubule growth and stability](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
8. [Identification of a ZEB2-MITF-ZEB1 transcriptional network that controls melanogenesis and melanoma progression](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
9. [Fezl is required for the birth and specification of corticospinal motor neurons](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
10. [Complementary expression pattern of Zfhx1 genes Sip1 and deltaEF1 in the mouse embryo and their genetic interaction revealed by compound mutants](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
11. [Regulation of ocular lens development by Smad-interacting protein 1 involving Foxe3 activation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
12. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q9R0G7&geneProductId=UniProtKB:Q9R0G7)
13. [Smad-interacting protein-1 (Zfhx1b) acts upstream of Wnt signaling in the mouse hippocampus and controls its formation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
14. [Mice lacking ZFHX1B, the gene that codes for Smad-interacting protein-1, reveal a role for multiple neural crest cell defects in the etiology of Hirschsprung disease-mental retardation syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q9R0G7)
15. ensembl Release 106