VGLL4
vestigial like family member 4
Summary
Predicted to enable transcription coactivator binding activity. Involved in negative regulation of Wnt signaling pathway; negative regulation of cell growth; and negative regulation of hippo signaling. Predicted to be located in nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants35 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2470423590 | 3:11,600,066 | C/G | — | uncertain significance |
| rs377034464 | 3:11,600,101 | G/A | — | uncertain significance |
| rs763815966 | 3:11,600,230 | C/T | — | uncertain significance |
| rs550826126 | 3:11,600,820 | C/T | — | uncertain significance |
| rs771714714 | 3:11,600,836 | C/T | — | uncertain significance |
| rs369969148 | 3:11,600,901 | G/A | — | uncertain significance |
| rs775415280 | 3:11,606,302 | G/A | — | uncertain significance |
| rs754296543 | 3:11,606,309 | C/G | — | uncertain significance |
| rs765522686 | 3:11,606,314 | G/A | — | uncertain significance |
| rs750870490 | 3:11,606,324 | C/T | — | uncertain significance |
| rs754575118 | 3:11,606,325 | G/A | — | likely benign |
| rs868364435 | 3:11,606,342 | T/C | — | uncertain significance |
| rs964703248 | 3:11,606,383 | G/A | — | uncertain significance |
| rs889298834 | 3:11,606,384 | T/C | — | likely benign |
| rs747220655 | 3:11,606,399 | C/T | — | uncertain significance |
| rs765792252 | 3:11,606,409 | C/T | — | uncertain significance |
| rs778954240 | 3:11,606,429 | G/A | — | uncertain significance |
| rs200844511 | 3:11,606,444 | G/A | — | uncertain significance |
| rs774581253 | 3:11,606,456 | G/A | — | uncertain significance |
| rs373201873 | 3:11,606,468 | G/A | — | uncertain significance |
| rs6802119 | 3:11,625,414 | C/G | — | — |
| rs9870506 | 3:11,635,631 | C/A | regulatory region variant | — |
| rs2574727 | 3:11,636,508 | G/A | intron variant | — |
| rs62248289 | 3:11,637,907 | T/C | regulatory region variant | — |
| rs6780175 | 3:11,638,519 | G/T | — | — |
| rs2470725854 | 3:11,643,353 | C/T | — | uncertain significance |
| rs148585381 | 3:11,643,416 | G/A | — | uncertain significance |
| rs1364806914 | 3:11,643,422 | C/T | — | uncertain significance |
| rs751730160 | 3:11,643,454 | G/T | — | uncertain significance |
| rs2443724 | 3:11,655,351 | C/G | downstream gene variant | — |
| rs2616559 | 3:11,657,848 | G/A | downstream gene variant | — |
| rs6782029 | 3:11,675,789 | T/G | — | — |
| rs2437687 | 3:11,680,693 | G/A | — | — |
| rs4684792 | 3:11,694,467 | T/A | — | — |
| rs746283007 | 3:11,744,459 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.