FOXL1
forkhead box L1
Summary
This gene encodes a member of the forkhead/winged helix-box (FOX) family of transcription factors. FOX transcription factors are characterized by a distinct DNA-binding forkhead domain and play critical roles in the regulation of multiple processes including metabolism, cell proliferation and gene expression during ontogenesis. [provided by RefSeq, Nov 2012]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs191469137 | 16:86,611,593 | G/C | regulatory region variant | — |
| rs1056333251 | 16:86,612,369 | G/T | — | uncertain significance |
| rs142168655 | 16:86,612,378 | A/T | — | uncertain significance |
| rs151159060 | 16:86,612,388 | T/C | — | uncertain significance |
| rs2507954290 | 16:86,612,405 | C/G | — | uncertain significance |
| rs779829411 | 16:86,612,439 | C/T | — | uncertain significance |
| rs200674245 | 16:86,612,505 | C/T | — | uncertain significance |
| rs2507954555 | 16:86,612,573 | C/T | — | uncertain significance |
| rs762059430 | 16:86,612,592 | A/T | — | uncertain significance |
| rs141410677 | 16:86,612,708 | C/T | — | uncertain significance |
| rs374413539 | 16:86,612,780 | G/A | — | uncertain significance |
| rs537362211 | 16:86,612,787 | A/C | — | uncertain significance |
| rs1296237840 | 16:86,612,804 | G/T | — | uncertain significance |
| rs1021757346 | 16:86,612,822 | A/G | — | likely benign |
| rs2507955035 | 16:86,612,828 | G/A | — | uncertain significance |
| rs751373929 | 16:86,612,837 | C/T | — | uncertain significance |
| rs545875290 | 16:86,612,838 | C/A | — | uncertain significance |
| rs1437058351 | 16:86,612,840 | G/A | — | uncertain significance |
| rs924397043 | 16:86,612,915 | C/T | — | uncertain significance |
| rs771036897 | 16:86,612,954 | C/T | — | uncertain significance |
| rs796781281 | 16:86,612,970 | C/G | — | uncertain significance |
| rs1031965178 | 16:86,612,994 | C/T | — | likely benign |
| rs748648044 | 16:86,612,999 | G/A | — | uncertain significance |
| rs1273338441 | 16:86,613,056 | C/T | — | uncertain significance |
| rs1217767449 | 16:86,613,134 | G/A | — | uncertain significance |
| rs775985911 | 16:86,613,169 | A/C | — | uncertain significance |
| rs188450396 | 16:86,613,173 | C/A | — | uncertain significance |
| rs1051734980 | 16:86,613,187 | G/T | — | uncertain significance |
| rs369054293 | 16:86,613,242 | C/G | — | uncertain significance |
| rs778077859 | 16:86,613,356 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.