RNFT2
ring finger protein, transmembrane 2
Summary
Predicted to enable ubiquitin protein ligase activity. Predicted to be involved in positive regulation of ERAD pathway. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs374588096 | 12:117,178,308 | G/T | — | uncertain significance |
| rs996313242 | 12:117,187,651 | G/A | — | uncertain significance |
| rs1165338485 | 12:117,187,660 | C/T | — | uncertain significance |
| rs750674190 | 12:117,187,675 | C/T | — | uncertain significance |
| rs2500200551 | 12:117,187,806 | G/C | — | uncertain significance |
| rs550229046 | 12:117,187,920 | G/A | — | uncertain significance |
| rs1312754435 | 12:117,187,923 | C/T | — | uncertain significance |
| rs763132330 | 12:117,187,978 | A/T | — | uncertain significance |
| rs372050554 | 12:117,187,989 | G/A | — | uncertain significance |
| rs2500203374 | 12:117,188,088 | A/G | — | uncertain significance |
| rs751624015 | 12:117,191,824 | G/A | — | uncertain significance |
| rs12322695 | 12:117,199,414 | G/T | intron variant | — |
| rs146270391 | 12:117,204,676 | C/G | — | uncertain significance |
| rs1317829414 | 12:117,217,041 | T/C | — | uncertain significance |
| rs1295766809 | 12:117,217,056 | T/C | — | uncertain significance |
| rs754857107 | 12:117,217,129 | G/C | — | uncertain significance |
| rs4767458 | 12:117,258,178 | T/G | — | — |
| rs10850722 | 12:117,259,276 | C/G | intron variant | — |
| rs1435650420 | 12:117,271,679 | T/C | — | uncertain significance |
| rs757334013 | 12:117,273,766 | C/G | — | uncertain significance |
| rs370793327 | 12:117,273,780 | G/A | — | uncertain significance |
| rs2499873720 | 12:117,273,781 | G/A | — | uncertain significance |
| rs748142706 | 12:117,273,999 | G/A | — | uncertain significance |
| rs764857827 | 12:117,274,007 | G/A | — | uncertain significance |
| rs1483395622 | 12:117,274,028 | G/A | — | uncertain significance |
| rs533778630 | 12:117,274,055 | G/A | — | uncertain significance |
| rs143841382 | 12:117,283,027 | T/G | intron variant | — |
| rs7298450 | 12:117,285,279 | C/T | — | — |
| rs2499893328 | 12:117,287,129 | G/C | — | uncertain significance |
| rs1372684864 | 12:117,287,159 | G/A | — | uncertain significance |
| rs903775 | 12:117,289,613 | G/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.