RC3H2

ring finger and CCCH-type domains 2

Summary

Enables DNA binding activity; RNA binding activity; and ubiquitin protein ligase activity. Involved in protein polyubiquitination. Located in cell surface; intracellular membrane-bounded organelle; and membrane. [provided by Alliance of Genome Resources, Apr 2025]

Known Variants42 total

rsidPosition (GRCh37)AllelesClassClinVar
rs12301711879:125,611,970A/Cuncertain significance
rs3773493989:125,611,973T/Guncertain significance
rs15880456149:125,612,073T/Cuncertain significance
rs7647242249:125,612,078G/Cuncertain significance
rs48380189:125,612,807C/G
rs3718375149:125,613,432T/Guncertain significance
rs5588324469:125,613,684T/Cuncertain significance
rs571402279:125,614,617T/Cintron variant
rs25381758929:125,616,335C/Tuncertain significance
rs7761082589:125,616,540C/Tuncertain significance
rs1412379819:125,617,668G/Cuncertain significance
rs25381811509:125,618,052C/Tuncertain significance
rs13823651859:125,618,145C/Tuncertain significance
rs3688280689:125,620,209C/Tuncertain significance
rs9434145899:125,620,221C/Tuncertain significance
rs3772886009:125,620,305T/Cuncertain significance
rs7760573399:125,620,991C/Tuncertain significance
rs3740476369:125,621,000G/Auncertain significance
rs5486759049:125,621,034G/Auncertain significance
rs15880582399:125,621,067C/Auncertain significance
rs3714865669:125,621,201G/Auncertain significance
rs3747153159:125,621,235G/Cuncertain significance
rs9157310819:125,621,366G/Auncertain significance
rs27929909:125,621,610G/Cintron variant
rs7606770369:125,622,230C/Guncertain significance
rs25381929799:125,622,283C/Tuncertain significance
rs25381930719:125,622,305G/Cuncertain significance
rs2009649149:125,622,311T/Guncertain significance
rs7686927569:125,622,312T/Auncertain significance
rs12694462539:125,622,391T/Cuncertain significance
rs1172948099:125,627,639A/Clikely benign
rs5364460389:125,627,736C/Tuncertain significance
rs10334444439:125,627,791G/Cuncertain significance
rs1389708459:125,627,910T/Cuncertain significance
rs563405439:125,637,584A/Clikely benign
rs7675664769:125,642,114T/Cuncertain significance
rs2018581929:125,642,305A/Cuncertain significance
rs13895873149:125,642,982A/Cuncertain significance
rs25382778169:125,645,638T/Cuncertain significance
rs25382937519:125,652,641G/Auncertain significance
rs25382938849:125,652,707C/Tuncertain significance
rs7773068359:125,652,815C/Guncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.