ELF1
E74 like ETS transcription factor 1
Summary
This gene encodes an E26 transformation-specific related transcription factor. The encoded protein is primarily expressed in lymphoid cells and acts as both an enhancer and a repressor to regulate transcription of various genes. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2009]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs115657038 | 13:41,507,579 | C/T | — | benign |
| rs1414765344 | 13:41,507,583 | A/T | — | uncertain significance |
| rs140656224 | 13:41,507,585 | T/A | — | uncertain significance |
| rs144467943 | 13:41,507,586 | T/G | — | uncertain significance |
| rs368677066 | 13:41,507,655 | G/A | — | uncertain significance |
| rs772158393 | 13:41,507,664 | T/C | — | uncertain significance |
| rs150015002 | 13:41,507,769 | G/A | — | uncertain significance |
| rs773346594 | 13:41,507,772 | C/T | — | uncertain significance |
| rs751176591 | 13:41,507,824 | G/A | — | uncertain significance |
| rs779828314 | 13:41,507,863 | C/T | — | uncertain significance |
| rs778799774 | 13:41,507,889 | T/C | — | uncertain significance |
| rs544414935 | 13:41,507,895 | G/T | — | uncertain significance |
| rs749478443 | 13:41,508,026 | C/A | — | uncertain significance |
| rs756235921 | 13:41,508,124 | G/A | — | uncertain significance |
| rs997506425 | 13:41,515,157 | C/G | — | uncertain significance |
| rs751945909 | 13:41,515,189 | T/A | — | uncertain significance |
| rs764212056 | 13:41,515,202 | C/T | — | uncertain significance |
| rs751972706 | 13:41,515,207 | C/T | — | uncertain significance |
| rs151034333 | 13:41,515,221 | T/A | — | benign |
| rs2546968794 | 13:41,515,237 | A/C | — | uncertain significance |
| rs571253522 | 13:41,515,273 | G/A | — | uncertain significance |
| rs146850967 | 13:41,515,324 | C/T | — | uncertain significance |
| rs144532940 | 13:41,515,345 | C/G | — | uncertain significance |
| rs774343467 | 13:41,515,372 | G/A | — | uncertain significance |
| rs773668917 | 13:41,515,376 | G/A | — | uncertain significance |
| rs2546969043 | 13:41,515,391 | T/C | — | uncertain significance |
| rs1032880556 | 13:41,515,422 | T/C | — | uncertain significance |
| rs777535025 | 13:41,515,433 | T/C | — | uncertain significance |
| rs1870340367 | 13:41,518,007 | G/C | — | uncertain significance |
| rs75719223 | 13:41,522,272 | T/G | intron variant | — |
| rs138109960 | 13:41,523,980 | G/A | — | uncertain significance |
| rs752065082 | 13:41,525,486 | T/C | — | uncertain significance |
| rs1350852775 | 13:41,525,506 | T/C | — | uncertain significance |
| rs960503567 | 13:41,525,542 | G/A | — | uncertain significance |
| rs9566635 | 13:41,528,890 | A/C | — | — |
| rs140074062 | 13:41,531,787 | C/T | intron variant | — |
| rs2546989276 | 13:41,533,083 | A/G | — | uncertain significance |
| rs9594466 | 13:41,533,981 | T/C | intron variant | — |
| rs8001208 | 13:41,537,851 | T/A | — | — |
| rs11147831 | 13:41,552,729 | G/A | intron variant | — |
| rs7329174 | 13:41,558,110 | A/G | regulatory region variant | — |
| rs9566645 | 13:41,563,026 | T/A | — | — |
| rs57141708 | 13:41,575,391 | G/A | intron variant | — |
| rs7323613 | 13:41,581,666 | C/A | regulatory region variant | — |
| rs9805742 | 13:41,593,758 | A/G | upstream gene variant | — |
| rs9532707 | 13:41,600,687 | G/C | intron variant | — |
| rs73176948 | 13:41,611,271 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.