This gene encodes a ubiquitous transcriptional enhancer factor that is a member of the TEA/ATTS domain family. This protein directs the transactivation of a wide variety of genes and, in placental cells, also acts as a transcriptional repressor. Mutations in this gene cause Sveinsson's chorioretinal atrophy. Additional transcript variants have been described but their full-length natures have not been experimentally verified.,TEAD1,AA,NTEF-1,REF1,TCF-13,TCF13,TEAD-1,TEF-1,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,Cell Adhesion,Hippo Signaling Pathway,Wnt/β-Catenin Signaling Pathway,Cardiovascular,Heart,Cardiogenesis,TEAD1