NEURL1
neuralized E3 ubiquitin protein ligase 1
Summary
Predicted to enable translation factor activity, non-nucleic acid binding and ubiquitin protein ligase activity. Involved in negative regulation of Notch signaling pathway; negative regulation of cell population proliferation; and positive regulation of apoptotic process. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants59 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs180841058 | 10:105,255,447 | G/A | intron variant | — |
| rs7071247 | 10:105,257,786 | G/T | intron variant | — |
| rs7068167 | 10:105,293,585 | T/A | — | — |
| rs7069733 | 10:105,297,770 | C/G | intron variant | — |
| rs6584555 | 10:105,299,611 | T/C | intron variant | — |
| rs192132529 | 10:105,305,226 | A/T | upstream gene variant | — |
| rs12415501 | 10:105,324,774 | C/T | regulatory region variant | — |
| rs759183606 | 10:105,330,688 | T/C | — | uncertain significance |
| rs764822553 | 10:105,330,689 | G/A | — | uncertain significance |
| rs1027115656 | 10:105,330,710 | G/T | — | uncertain significance |
| rs545506384 | 10:105,330,745 | C/T | — | uncertain significance |
| rs2540823898 | 10:105,330,787 | G/T | — | uncertain significance |
| rs12253987 | 10:105,330,947 | T/A | intron variant | — |
| rs778447200 | 10:105,331,284 | C/T | — | likely benign |
| rs535287090 | 10:105,331,325 | G/A | — | uncertain significance |
| rs1481561610 | 10:105,331,412 | T/G | — | uncertain significance |
| rs144267741 | 10:105,331,418 | A/G | — | uncertain significance |
| rs201585235 | 10:105,331,435 | G/T | — | uncertain significance |
| rs765005636 | 10:105,331,489 | G/A | — | uncertain significance |
| rs769464925 | 10:105,331,517 | C/T | — | uncertain significance |
| rs751012519 | 10:105,331,561 | C/T | — | uncertain significance |
| rs377333331 | 10:105,331,567 | G/A | — | uncertain significance |
| rs185158502 | 10:105,334,707 | A/G | regulatory region variant | — |
| rs3781370 | 10:105,335,156 | T/C | intron variant | — |
| rs373205748 | 10:105,335,361 | C/T | — | — |
| rs77260060 | 10:105,338,726 | G/A | regulatory region variant | — |
| rs1469732629 | 10:105,344,368 | A/C | — | uncertain significance |
| rs776984066 | 10:105,344,433 | G/C | — | uncertain significance |
| rs1226047168 | 10:105,344,479 | A/T | — | uncertain significance |
| rs2540832257 | 10:105,344,485 | A/G | — | uncertain significance |
| rs781706160 | 10:105,344,501 | G/A | — | likely benign |
| rs1191556438 | 10:105,344,503 | C/T | — | uncertain significance |
| rs746345166 | 10:105,344,512 | T/C | — | uncertain significance |
| rs1468042390 | 10:105,344,515 | A/G | — | uncertain significance |
| rs770177521 | 10:105,344,517 | G/C | — | uncertain significance |
| rs2540832337 | 10:105,344,521 | A/C | — | uncertain significance |
| rs1398897124 | 10:105,344,531 | C/G | — | uncertain significance |
| rs2133885049 | 10:105,344,554 | A/C | — | uncertain significance |
| rs1021814478 | 10:105,344,581 | T/C | — | uncertain significance |
| rs2133885098 | 10:105,344,605 | A/G | — | uncertain significance |
| rs1220784776 | 10:105,344,622 | T/C | — | uncertain significance |
| rs2540832525 | 10:105,344,634 | C/G | — | uncertain significance |
| rs924900960 | 10:105,344,637 | G/A | — | uncertain significance |
| rs1336497069 | 10:105,344,730 | G/A | — | uncertain significance |
| rs772791675 | 10:105,344,734 | C/T | — | uncertain significance |
| rs1463907930 | 10:105,344,742 | C/T | — | uncertain significance |
| rs2035885043 | 10:105,344,779 | A/G | — | uncertain significance |
| rs371723689 | 10:105,344,897 | C/A | — | likely benign |
| rs1853842 | 10:105,348,493 | G/A | synonymous variant | — |
| rs753290267 | 10:105,349,288 | G/A | — | uncertain significance |
| rs775661307 | 10:105,349,291 | C/T | — | uncertain significance |
| rs759066315 | 10:105,349,337 | C/T | — | uncertain significance |
| rs751427809 | 10:105,349,345 | G/A | — | uncertain significance |
| rs17855518 | 10:105,349,357 | C/T | — | uncertain significance |
| rs749439690 | 10:105,349,369 | C/T | — | uncertain significance |
| rs762189690 | 10:105,349,382 | C/T | — | uncertain significance |
| rs201432237 | 10:105,349,385 | G/A | — | uncertain significance |
| rs755198069 | 10:105,349,927 | C/T | — | uncertain significance |
| rs2133888081 | 10:105,349,939 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.