FOXP4
forkhead box P4
Summary
This gene belongs to subfamily P of the forkhead box (FOX) transcription factor family. Forkhead box transcription factors play important roles in the regulation of tissue- and cell type-specific gene transcription during both development and adulthood. Many members of the forkhead box gene family, including members of subfamily P, have roles in mammalian oncogenesis. This gene may play a role in the development of tumors of the kidney and larynx. Alternative splicing of this gene produces multiple transcript variants, some encoding different isoforms. [provided by RefSeq, Jul 2008]
Known Variants69 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs6935446 | 6:41,514,372 | A/G | regulatory region variant | — |
| rs2532622086 | 6:41,514,734 | G/C | — | uncertain significance |
| rs2532622760 | 6:41,514,834 | T/C | — | uncertain significance |
| rs9394807 | 6:41,517,484 | A/G | upstream gene variant | — |
| rs4714481 | 6:41,521,110 | T/C | upstream gene variant | — |
| rs4714482 | 6:41,528,199 | G/A | regulatory region variant | — |
| rs4714483 | 6:41,528,214 | G/A | regulatory region variant | — |
| rs9369290 | 6:41,533,046 | C/A | — | — |
| rs2532758243 | 6:41,533,322 | C/A | — | uncertain significance |
| rs2127349265 | 6:41,533,508 | G/T | — | likely pathogenic |
| rs779715276 | 6:41,533,545 | G/A | — | uncertain significance |
| rs139750093 | 6:41,533,556 | G/A | — | uncertain significance |
| rs34730847 | 6:41,533,573 | G/A | — | benign |
| rs2104506 | 6:41,533,579 | C/A | — | benign |
| rs41273784 | 6:41,533,595 | G/A | — | likely benign |
| rs149026195 | 6:41,533,602 | C/T | — | uncertain significance |
| rs370054490 | 6:41,533,623 | C/T | — | uncertain significance |
| rs769065139 | 6:41,533,632 | A/G | — | uncertain significance |
| rs1764856579 | 6:41,533,691 | C/T | — | uncertain significance |
| rs1983891 | 6:41,536,427 | C/G | — | — |
| rs7761231 | 6:41,537,344 | G/A | regulatory region variant | — |
| rs4714486 | 6:41,542,417 | C/T | intron variant | — |
| rs778234827 | 6:41,545,740 | G/A | — | uncertain significance |
| rs6917270 | 6:41,548,755 | A/G | intron variant | — |
| rs148022939 | 6:41,553,201 | G/A | — | likely benign |
| rs141899153 | 6:41,553,213 | G/T | — | uncertain significance |
| rs954727990 | 6:41,554,533 | T/C | — | uncertain significance |
| rs2532399319 | 6:41,554,606 | G/T | — | uncertain significance |
| rs1447274580 | 6:41,554,822 | A/C | — | uncertain significance |
| rs2532402217 | 6:41,554,883 | C/A | — | uncertain significance |
| rs199908081 | 6:41,555,111 | G/A | — | uncertain significance |
| rs781449571 | 6:41,555,142 | C/A | — | uncertain significance |
| rs758748324 | 6:41,555,168 | G/A | — | uncertain significance |
| rs377455960 | 6:41,555,192 | C/T | — | uncertain significance |
| rs753448087 | 6:41,555,193 | T/A | — | uncertain significance |
| rs35584312 | 6:41,555,212 | C/T | — | benign |
| rs2532408943 | 6:41,555,562 | C/G | — | uncertain significance |
| rs1766247978 | 6:41,555,587 | A/G | — | uncertain significance |
| rs2532416003 | 6:41,556,431 | C/T | — | uncertain significance |
| rs951046741 | 6:41,557,541 | G/A | — | uncertain significance |
| rs1380556802 | 6:41,557,586 | C/A | — | uncertain significance |
| rs116314747 | 6:41,557,708 | C/T | — | benign |
| rs2532425822 | 6:41,557,767 | G/A | — | uncertain significance |
| rs762813932 | 6:41,557,776 | G/A | — | uncertain significance |
| rs767113603 | 6:41,557,797 | G/A | — | uncertain significance |
| rs1308773151 | 6:41,557,819 | G/T | — | uncertain significance |
| rs533563759 | 6:41,557,860 | C/T | — | uncertain significance |
| rs2532427429 | 6:41,557,910 | T/G | — | not provided |
| rs377548372 | 6:41,558,019 | G/C | — | uncertain significance |
| rs778609898 | 6:41,558,080 | C/T | — | uncertain significance |
| rs3800283 | 6:41,558,358 | A/G | intron variant | — |
| rs1390275782 | 6:41,558,974 | C/G | — | uncertain significance |
| rs2127404974 | 6:41,562,611 | G/A | — | pathogenic |
| rs749742109 | 6:41,565,522 | G/T | — | uncertain significance |
| rs2532472563 | 6:41,565,558 | C/A | — | uncertain significance |
| rs143078501 | 6:41,565,566 | G/A | — | uncertain significance |
| rs147769655 | 6:41,565,581 | C/T | — | benign |
| rs141279563 | 6:41,565,582 | G/A | — | likely benign |
| rs994262167 | 6:41,565,592 | T/C | — | uncertain significance |
| rs1386593461 | 6:41,565,605 | C/G | — | uncertain significance |
| rs770662735 | 6:41,565,627 | G/A | — | uncertain significance |
| rs964209005 | 6:41,565,648 | G/A | — | uncertain significance |
| rs766679556 | 6:41,565,667 | G/A | — | uncertain significance |
| rs755365713 | 6:41,565,676 | C/T | — | uncertain significance |
| rs370843267 | 6:41,566,530 | C/A | — | uncertain significance |
| rs918576584 | 6:41,566,544 | A/C | — | uncertain significance |
| rs747762632 | 6:41,566,582 | G/A | — | uncertain significance |
| rs761964285 | 6:41,566,598 | C/T | — | uncertain significance |
| rs777107637 | 6:41,566,644 | G/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.