TEAD2
TEA domain transcription factor 2
Summary
Enables several functions, including DNA-binding transcription factor activity; disordered domain specific binding activity; and transcription coactivator binding activity. Involved in hippo signaling; positive regulation of DNA-templated transcription; and protein-containing complex assembly. Located in cytosol and nucleoplasm. Part of TEAD-YAP complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs775244653 | 19:49,845,721 | C/T | — | uncertain significance |
| rs1329997633 | 19:49,845,763 | G/T | — | uncertain significance |
| rs553489773 | 19:49,846,631 | C/T | — | uncertain significance |
| rs553770323 | 19:49,849,078 | G/A | — | — |
| rs572680697 | 19:49,850,484 | C/T | — | uncertain significance |
| rs112401023 | 19:49,851,423 | A/C | regulatory region variant | — |
| rs199768067 | 19:49,851,979 | G/A | — | uncertain significance |
| rs75100029 | 19:49,852,030 | C/G | — | benign |
| rs375675782 | 19:49,852,033 | C/T | — | uncertain significance |
| rs201482323 | 19:49,852,054 | G/A | — | uncertain significance |
| rs760225003 | 19:49,852,061 | T/G | — | uncertain significance |
| rs201393859 | 19:49,852,070 | G/A | — | benign |
| rs779204844 | 19:49,852,097 | C/T | — | uncertain significance |
| rs6509428 | 19:49,853,881 | C/T | intron variant | — |
| rs1052878203 | 19:49,854,578 | G/A | — | uncertain significance |
| rs144101841 | 19:49,854,620 | A/G | — | uncertain significance |
| rs752314728 | 19:49,857,215 | T/G | — | — |
| rs755722493 | 19:49,858,616 | T/C | — | uncertain significance |
| rs80095365 | 19:49,860,521 | C/A | — | benign |
| rs780574546 | 19:49,860,543 | C/G | — | uncertain significance |
| rs766550565 | 19:49,863,196 | C/T | — | uncertain significance |
| rs140532469 | 19:49,863,224 | C/T | — | uncertain significance |
| rs368557340 | 19:49,863,283 | G/A | — | uncertain significance |
| rs746559026 | 19:49,863,307 | G/A | — | uncertain significance |
| rs775655818 | 19:49,863,320 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.