RNF115
ring finger protein 115
Summary
Enables ubiquitin protein ligase activity. Involved in negative regulation of signal transduction; protein ubiquitination; and ubiquitin-dependent protein catabolic process via the multivesicular body sorting pathway. Is active in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2526107057 | 1:145,611,319 | G/A | — | uncertain significance |
| rs781849682 | 1:145,611,324 | G/A | — | uncertain significance |
| rs61816194 | 1:145,614,468 | C/T | upstream gene variant | — |
| rs141084774 | 1:145,639,731 | G/T | — | — |
| rs11583404 | 1:145,640,157 | T/C | intron variant | — |
| rs12405132 | 1:145,644,984 | C/T | intron variant | — |
| rs12744221 | 1:145,645,606 | C/A | — | — |
| rs1553718532 | 1:145,646,121 | A/C | — | uncertain significance |
| rs76450533 | 1:145,648,485 | A/G | intron variant | — |
| rs781914601 | 1:145,650,508 | A/T | — | uncertain significance |
| rs10797658 | 1:145,651,246 | T/A | intron variant | — |
| rs782425145 | 1:145,663,229 | A/G | — | uncertain significance |
| rs782436435 | 1:145,663,310 | G/T | — | uncertain significance |
| rs377326453 | 1:145,663,340 | G/A | — | uncertain significance |
| rs1647649950 | 1:145,663,357 | G/A | — | uncertain significance |
| rs782188005 | 1:145,663,360 | A/G | — | uncertain significance |
| rs142882762 | 1:145,671,122 | A/C | intron variant | — |
| rs35687015 | 1:145,674,149 | T/C | — | — |
| rs782416502 | 1:145,682,090 | T/G | — | uncertain significance |
| rs782644559 | 1:145,683,579 | G/A | — | uncertain significance |
| rs782187405 | 1:145,683,592 | C/T | — | uncertain significance |
| rs75203621 | 1:145,684,115 | C/T | intron variant | — |
| rs782088792 | 1:145,686,979 | T/A | — | uncertain significance |
| rs2525755054 | 1:145,686,981 | G/C | — | uncertain significance |
| rs1553711991 | 1:145,687,041 | C/G | — | uncertain significance |
| rs1553711974 | 1:145,687,078 | C/T | — | uncertain significance |
| rs143101667 | 1:145,688,131 | G/A | — | uncertain significance |
| rs1553711807 | 1:145,688,200 | C/T | — | uncertain significance |
| rs75485498 | 1:145,694,520 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.