PM20D2

peptidase M20 domain containing 2

Summary

Enables dipeptidase activity and identical protein binding activity. Acts upstream of or within proteolysis and regulation of protein metabolic process. Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants38 total

rsidPosition (GRCh37)AllelesClassClinVar
rs5608193786:89,801,734A/G——
rs94511486:89,806,992A/C3 prime UTR variant—
rs64547396:89,852,534G/Aupstream gene variant—
rs1443307436:89,852,656T/C——
rs7712089876:89,855,889T/C—uncertain significance
rs14567803716:89,855,892A/C—uncertain significance
rs25334900486:89,855,919A/T—uncertain significance
rs7661010026:89,855,939C/T—uncertain significance
rs7459341526:89,856,014C/G—uncertain significance
rs3737599716:89,856,015T/A—uncertain significance
rs7647033706:89,856,077G/A—uncertain significance
rs25334920086:89,856,120C/G—uncertain significance
rs9419751186:89,856,152C/G—uncertain significance
rs5435513036:89,856,159C/G—uncertain significance
rs10390285756:89,856,194C/T—uncertain significance
rs12573442066:89,856,224G/C—uncertain significance
rs3703803596:89,856,251G/T—uncertain significance
rs9990798556:89,856,263G/T—uncertain significance
rs10167330436:89,856,294T/C—uncertain significance
rs12771211486:89,856,320C/T—uncertain significance
rs12805960766:89,856,323G/T—uncertain significance
rs2010105106:89,858,991T/C—uncertain significance
rs25335062196:89,859,067T/A—uncertain significance
rs25335063656:89,859,096A/G—uncertain significance
rs12698332356:89,859,101G/A—uncertain significance
rs1430541536:89,860,650A/Gintron variant—
rs3775657606:89,862,769G/T—uncertain significance
rs5542948636:89,864,487G/A—uncertain significance
rs25335227206:89,864,488T/G—uncertain significance
rs1418269046:89,868,090A/G—uncertain significance
rs2013128276:89,868,156A/G—uncertain significance
rs25335405116:89,871,585A/G—uncertain significance
rs7690847436:89,871,893G/A—uncertain significance
rs1428230726:89,871,913A/C—uncertain significance
rs1445878166:89,871,937T/A—uncertain significance
rs7536155636:89,871,959C/G—likely benign
rs13845445156:89,871,962T/C—uncertain significance
rs1140421856:89,873,284G/A3 prime UTR variant—

Gene information from NCBI Gene. Variant classifications from ClinVar.