ELL
elongation factor for RNA polymerase II
Summary
Enables phosphatase binding activity. Involved in positive regulation of DNA-templated transcription and snRNA transcription. Located in cytosol; euchromatin; and nuclear body. Part of transcription elongation factor complex. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants54 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150693262 | 19:18,555,668 | T/C | — | uncertain significance |
| rs898873884 | 19:18,556,069 | C/T | — | uncertain significance |
| rs778608559 | 19:18,557,160 | C/T | — | uncertain significance |
| rs1177176329 | 19:18,557,163 | C/T | — | uncertain significance |
| rs1313567339 | 19:18,557,588 | G/C | — | uncertain significance |
| rs34010330 | 19:18,559,657 | G/C | intron variant | — |
| rs748609 | 19:18,560,282 | T/G | — | — |
| rs770568039 | 19:18,561,352 | C/T | — | uncertain significance |
| rs370344034 | 19:18,561,360 | G/C | — | uncertain significance |
| rs751965470 | 19:18,561,370 | G/A | — | uncertain significance |
| rs34868531 | 19:18,561,473 | G/A | — | benign |
| rs756997423 | 19:18,561,475 | C/G | — | uncertain significance |
| rs200447123 | 19:18,561,476 | C/T | — | likely benign |
| rs1217135261 | 19:18,561,536 | G/A | — | uncertain significance |
| rs566474553 | 19:18,561,580 | G/A | — | uncertain significance |
| rs775735364 | 19:18,561,632 | T/C | — | likely benign |
| rs773155395 | 19:18,561,646 | G/A | — | uncertain significance |
| rs757695728 | 19:18,561,680 | C/T | — | likely benign |
| rs368841070 | 19:18,561,758 | C/T | — | uncertain significance |
| rs904550653 | 19:18,561,772 | G/A | — | uncertain significance |
| rs755150855 | 19:18,561,782 | G/A | — | uncertain significance |
| rs868053773 | 19:18,562,372 | G/C | — | uncertain significance |
| rs759973204 | 19:18,562,388 | G/A | — | uncertain significance |
| rs2303694 | 19:18,562,438 | C/T | — | benign |
| rs1018173693 | 19:18,562,450 | C/G | — | uncertain significance |
| rs731945 | 19:18,567,039 | C/T | intron variant | — |
| rs10423802 | 19:18,567,901 | C/T | intron variant | — |
| rs749268169 | 19:18,569,025 | C/A | — | uncertain significance |
| rs4808801 | 19:18,571,141 | A/G | regulatory region variant | — |
| rs371932488 | 19:18,572,410 | G/A | — | uncertain significance |
| rs929866154 | 19:18,572,416 | T/C | — | uncertain significance |
| rs753377816 | 19:18,572,531 | C/T | — | uncertain significance |
| rs753183117 | 19:18,572,599 | C/T | — | uncertain significance |
| rs749441049 | 19:18,572,617 | G/A | — | uncertain significance |
| rs1036175719 | 19:18,576,362 | C/T | — | uncertain significance |
| rs777043107 | 19:18,576,637 | C/A | — | uncertain significance |
| rs202163999 | 19:18,576,648 | G/T | — | uncertain significance |
| rs1275749327 | 19:18,576,664 | T/C | — | uncertain significance |
| rs146396182 | 19:18,576,685 | G/A | — | uncertain significance |
| rs771450349 | 19:18,576,698 | C/T | — | likely benign |
| rs142979628 | 19:18,576,721 | G/A | — | uncertain significance |
| rs144320562 | 19:18,576,725 | T/C | — | uncertain significance |
| rs10419404 | 19:18,578,654 | T/A | — | — |
| rs10413922 | 19:18,578,689 | A/G | — | — |
| rs7253990 | 19:18,604,085 | C/G | intron variant | — |
| rs8107347 | 19:18,612,748 | G/A | intron variant | — |
| rs8107351 | 19:18,612,758 | G/A | intron variant | — |
| rs1469412 | 19:18,616,399 | T/C | regulatory region variant | — |
| rs4808136 | 19:18,618,867 | G/A | regulatory region variant | — |
| rs140067716 | 19:18,625,193 | G/A | intron variant | — |
| rs7252185 | 19:18,632,225 | T/C | regulatory region variant | — |
| rs573675461 | 19:18,632,841 | T/C | — | uncertain significance |
| rs781430794 | 19:18,632,844 | T/C | — | uncertain significance |
| rs769937636 | 19:18,632,846 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.