NOL11
nucleolar protein 11
Summary
Enables RNA binding activity. Involved in maturation of SSU-rRNA and positive regulation of transcription of nucleolar large rRNA by RNA polymerase I. Located in nucleolus. Part of t-UTP complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs761231053 | 17:65,714,074 | T/C | — | uncertain significance |
| rs201563517 | 17:65,714,081 | A/T | — | uncertain significance |
| rs751950512 | 17:65,714,082 | G/A | — | uncertain significance |
| rs761580184 | 17:65,714,109 | A/G | — | likely benign |
| rs2509945279 | 17:65,714,139 | G/A | — | uncertain significance |
| rs2509945309 | 17:65,714,161 | A/C | — | uncertain significance |
| rs758468472 | 17:65,714,210 | G/A | — | — |
| rs764429218 | 17:65,715,806 | C/G | — | uncertain significance |
| rs750560995 | 17:65,715,833 | G/A | — | uncertain significance |
| rs201484850 | 17:65,715,837 | A/T | — | uncertain significance |
| rs2509946597 | 17:65,715,853 | G/A | — | uncertain significance |
| rs753599497 | 17:65,715,875 | G/A | — | uncertain significance |
| rs369265180 | 17:65,715,881 | A/C | — | uncertain significance |
| rs368087259 | 17:65,716,052 | A/T | — | uncertain significance |
| rs568124045 | 17:65,717,524 | G/T | — | uncertain significance |
| rs200900858 | 17:65,717,556 | G/T | — | uncertain significance |
| rs1221694183 | 17:65,717,570 | G/A | — | uncertain significance |
| rs767192630 | 17:65,717,603 | A/G | — | uncertain significance |
| rs867599412 | 17:65,717,620 | A/G | — | uncertain significance |
| rs79434722 | 17:65,718,750 | A/G | — | benign |
| rs751845847 | 17:65,720,204 | C/G | — | uncertain significance |
| rs202096165 | 17:65,720,282 | C/T | — | uncertain significance |
| rs150949358 | 17:65,720,291 | A/G | — | uncertain significance |
| rs1238439782 | 17:65,720,302 | G/C | — | uncertain significance |
| rs2055094779 | 17:65,722,609 | C/T | — | uncertain significance |
| rs76234567 | 17:65,722,704 | C/G | — | benign |
| rs372938548 | 17:65,730,545 | C/T | — | uncertain significance |
| rs1245848160 | 17:65,732,026 | A/G | — | uncertain significance |
| rs1465662513 | 17:65,732,104 | G/A | — | uncertain significance |
| rs768143420 | 17:65,732,137 | C/G | — | uncertain significance |
| rs146115629 | 17:65,732,850 | T/C | — | uncertain significance |
| rs914018372 | 17:65,733,642 | A/G | — | uncertain significance |
| rs760769113 | 17:65,733,741 | G/T | — | uncertain significance |
| rs2055214830 | 17:65,733,750 | T/A | — | uncertain significance |
| rs2509958825 | 17:65,734,017 | A/C | — | uncertain significance |
| rs764690858 | 17:65,734,054 | T/A | — | uncertain significance |
| rs149869108 | 17:65,734,254 | C/T | — | uncertain significance |
| rs540705052 | 17:65,734,294 | A/G | — | uncertain significance |
| rs143893275 | 17:65,734,322 | A/C | — | uncertain significance |
| rs201494014 | 17:65,734,432 | G/T | — | uncertain significance |
| rs760153881 | 17:65,735,061 | C/T | — | uncertain significance |
| rs369956349 | 17:65,739,609 | A/G | — | uncertain significance |
| rs2509962207 | 17:65,739,677 | A/G | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.