ELK4
ETS transcription factor ELK4
Summary
This gene is a member of the Ets family of transcription factors and of the ternary complex factor (TCF) subfamily. Proteins of the TCF subfamily form a ternary complex by binding to the the serum response factor and the serum reponse element in the promoter of the c-fos proto-oncogene. The protein encoded by this gene is phosphorylated by the kinases, MAPK1 and MAPK8. Several transcript variants have been described for this gene. [provided by RefSeq, Jul 2008]
Known Variants24 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs181630769 | 1:205,577,580 | G/A | 3 prime UTR variant | — |
| rs750401968 | 1:205,581,886 | T/C | — | — |
| rs767228986 | 1:205,585,754 | T/A | — | uncertain significance |
| rs544747964 | 1:205,587,921 | A/T | — | — |
| rs942927780 | 1:205,589,125 | G/A | — | uncertain significance |
| rs1670302377 | 1:205,589,128 | G/C | — | uncertain significance |
| rs781197440 | 1:205,589,135 | A/G | — | uncertain significance |
| rs759155171 | 1:205,589,206 | T/C | — | uncertain significance |
| rs756989722 | 1:205,589,209 | G/C | — | uncertain significance |
| rs149593454 | 1:205,589,308 | G/C | — | uncertain significance |
| rs764492506 | 1:205,589,315 | A/G | — | uncertain significance |
| rs750123304 | 1:205,589,323 | G/A | — | uncertain significance |
| rs142937236 | 1:205,589,396 | G/T | — | uncertain significance |
| rs752658016 | 1:205,589,435 | T/C | — | likely benign |
| rs146453123 | 1:205,589,455 | G/A | — | uncertain significance |
| rs377088845 | 1:205,589,530 | G/C | — | uncertain significance |
| rs754056060 | 1:205,589,533 | A/G | — | uncertain significance |
| rs763834169 | 1:205,589,605 | T/C | — | uncertain significance |
| rs369067229 | 1:205,589,698 | T/C | — | uncertain significance |
| rs1382052163 | 1:205,589,819 | C/T | — | uncertain significance |
| rs778738301 | 1:205,589,884 | G/C | — | uncertain significance |
| rs2527287274 | 1:205,589,917 | G/A | — | uncertain significance |
| rs2527294366 | 1:205,592,959 | G/T | — | uncertain significance |
| rs564286049 | 1:205,595,114 | T/C | coding sequence variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.