# T-box transcription factor 5

> mammalian protein found in Homo sapiens

**Wikidata**: [Q21114550](https://www.wikidata.org/wiki/Q21114550)  
**Source**: https://4ort.xyz/entity/t-box-transcription-factor-5


## References

1. UniProt
2. [InterPro Release 71.0](http://www.ebi.ac.uk/interpro/protein/Q99593)
3. Q20641742
4. [Functional analysis of TBX5 missense mutations associated with Holt-Oram syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
5. [Tbx5 associates with Nkx2-5 and synergistically promotes cardiomyocyte differentiation](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
6. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
7. [A WW domain protein TAZ is a critical coactivator for TBX5, a transcription factor implicated in Holt-Oram syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
8. [Intermolecular Interactions of Cardiac Transcription Factors NKX2.5 and TBX5](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
9. [GATA4 loss-of-function mutations underlie familial tetralogy of fallot](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
10. [Acetylation of TBX5 by KAT2B and KAT2A regulates heart and limb development.](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
11. [GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
12. [β-Catenin-driven cancers require a YAP1 transcriptional complex for survival and tumorigenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
13. [A census of human transcription factors: function, expression and evolution](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
14. [Induction of apoptosis and inhibition of cell growth by developmental regulator hTBX5](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
15. [TBX5 nuclear localization is mediated by dual cooperative intramolecular signals](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
16. [Epicardial–Myocardial Signaling Directing Coronary Vasculogenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
17. [Mutations in human TBX5 [corrected] cause limb and cardiac malformation in Holt-Oram syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
18. [Holt-Oram syndrome is caused by mutations in TBX5, a member of the Brachyury (T) gene family](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
19. [TBX5 transcription factor regulates cell proliferation during cardiogenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
20. [GOA](http://www.ebi.ac.uk/QuickGO/annotations?protein=Q99593&geneProductId=UniProtKB:Q99593)
21. [A role for Tbx5 in proepicardial cell migration during cardiogenesis](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
22. [TBX5 genetic testing validates strict clinical criteria for Holt-Oram syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
23. [A novel TBX5 loss-of-function mutation associated with sporadic dilated cardiomyopathy](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
24. [TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome](http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q99593)
25. Ensembl Release 99