LONRF2
LON peptidase N-terminal domain and ring finger 2
Summary
Predicted to enable misfolded protein binding activity; ribonucleoprotein complex binding activity; and ubiquitin protein ligase activity. Predicted to act upstream of or within several processes, including motor behavior; neuron differentiation; and protein quality control for misfolded or incompletely synthesized proteins. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs746030640 | 2:100,900,797 | C/T | — | uncertain significance |
| rs775108359 | 2:100,900,812 | C/T | — | uncertain significance |
| rs890745575 | 2:100,900,866 | G/T | — | uncertain significance |
| rs1404543920 | 2:100,900,870 | T/C | — | uncertain significance |
| rs1390505386 | 2:100,900,879 | T/C | — | uncertain significance |
| rs746124886 | 2:100,900,896 | C/T | — | uncertain significance |
| rs771598045 | 2:100,900,913 | G/A | — | likely benign |
| rs1674857197 | 2:100,903,380 | G/A | — | uncertain significance |
| rs115462523 | 2:100,903,419 | A/G | — | uncertain significance |
| rs2466525135 | 2:100,903,424 | T/A | — | uncertain significance |
| rs373553931 | 2:100,903,437 | C/T | — | likely benign |
| rs762460147 | 2:100,903,438 | G/A | — | uncertain significance |
| rs748984983 | 2:100,906,797 | T/C | — | uncertain significance |
| rs771136972 | 2:100,906,809 | C/A | — | uncertain significance |
| rs2466532753 | 2:100,906,875 | C/G | — | uncertain significance |
| rs769566619 | 2:100,911,930 | T/C | — | uncertain significance |
| rs1002070490 | 2:100,911,951 | G/A | — | uncertain significance |
| rs116227203 | 2:100,911,980 | C/T | — | benign |
| rs116702638 | 2:100,915,330 | G/T | — | likely benign |
| rs759721719 | 2:100,916,202 | G/A | — | uncertain significance |
| rs1351027861 | 2:100,916,253 | C/T | — | uncertain significance |
| rs779861748 | 2:100,916,311 | G/A | — | uncertain significance |
| rs1675144326 | 2:100,916,340 | G/A | — | uncertain significance |
| rs569402017 | 2:100,916,343 | T/C | — | uncertain significance |
| rs1195478907 | 2:100,917,185 | T/C | — | uncertain significance |
| rs923949307 | 2:100,917,209 | T/C | — | uncertain significance |
| rs373599250 | 2:100,917,225 | C/T | — | uncertain significance |
| rs754317489 | 2:100,919,385 | T/C | — | uncertain significance |
| rs973564574 | 2:100,919,462 | C/T | — | uncertain significance |
| rs765291514 | 2:100,919,483 | G/A | — | uncertain significance |
| rs71413877 | 2:100,924,822 | G/A | intron variant | — |
| rs757787707 | 2:100,937,966 | A/C | — | uncertain significance |
| rs772001524 | 2:100,937,997 | G/T | — | uncertain significance |
| rs1458694611 | 2:100,938,150 | C/A | — | uncertain significance |
| rs1439556701 | 2:100,938,156 | G/T | — | uncertain significance |
| rs560279181 | 2:100,938,165 | C/T | — | likely benign |
| rs1223401305 | 2:100,938,212 | G/A | — | uncertain significance |
| rs1211986653 | 2:100,938,225 | G/A | — | uncertain significance |
| rs1317462997 | 2:100,938,243 | C/A | — | uncertain significance |
| rs1270226785 | 2:100,938,261 | C/T | — | uncertain significance |
| rs1675639429 | 2:100,938,309 | C/G | — | uncertain significance |
| rs776869605 | 2:100,938,381 | C/T | — | uncertain significance |
| rs1675644559 | 2:100,938,438 | C/G | — | uncertain significance |
| rs2104226788 | 2:100,938,454 | G/C | — | uncertain significance |
| rs1341991606 | 2:100,938,495 | C/T | — | uncertain significance |
| rs558772201 | 2:100,938,509 | C/T | — | uncertain significance |
| rs10183150 | 2:100,939,117 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.