MTMR11

myotubularin related protein 11

Summary

Predicted to enable phosphatidylinositol-3-phosphate phosphatase activity. Predicted to be involved in phosphatidylinositol dephosphorylation. Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants51 total

rsidPosition (GRCh37)AllelesClassClinVar
rs3734667601:149,901,032C/Auncertain significance
rs3734654411:149,901,095C/Tuncertain significance
rs7824220171:149,901,600G/Cuncertain significance
rs1483021191:149,901,648G/Cuncertain significance
rs3695392511:149,901,672G/Cuncertain significance
rs1396420771:149,901,676G/Cuncertain significance
rs1399344711:149,901,711G/Auncertain significance
rs7823807211:149,901,721G/Auncertain significance
rs9970033461:149,901,733G/Auncertain significance
rs1456594441:149,902,342C/Tmissense variant
rs726928161:149,902,588A/Gupstream gene variant
rs3677291691:149,902,689C/Tuncertain significance
rs15537676051:149,903,223C/Tuncertain significance
rs7825348361:149,903,243A/Cuncertain significance
rs7820708771:149,903,312C/Guncertain significance
rs7827901491:149,903,315C/Tuncertain significance
rs1456129321:149,903,853C/Tuncertain significance
rs20926662301:149,903,878A/Cuncertain significance
rs10229948041:149,904,177G/Auncertain significance
rs7826034491:149,904,189G/Auncertain significance
rs5877302611:149,904,199A/Guncertain significance
rs726928211:149,905,279G/Adownstream gene variant
rs15537681331:149,905,362C/Tuncertain significance
rs7827157041:149,905,400G/Cuncertain significance
rs7819909931:149,905,510C/Auncertain significance
rs7712383941:149,905,531C/Guncertain significance
rs7818438071:149,905,756G/Auncertain significance
rs7825101831:149,905,764T/Auncertain significance
rs1448087811:149,905,773C/Tuncertain significance
rs25251888181:149,905,815A/Tuncertain significance
rs20926930181:149,905,835G/Cuncertain significance
rs3688054161:149,906,114G/Auncertain significance
rs2016594401:149,906,151G/Auncertain significance
rs7818935021:149,906,364G/Auncertain significance
rs7823533411:149,906,386T/Cuncertain significance
rs7826286021:149,906,392C/Tuncertain significance
rs112053031:149,906,413T/Cmissense variant
rs3767857141:149,906,415G/Auncertain significance
rs20927046181:149,906,888C/Auncertain significance
rs3701276961:149,906,931C/Tuncertain significance
rs7820421181:149,906,932G/Auncertain significance
rs2020521501:149,906,992G/Auncertain significance
rs7823014731:149,907,016C/Auncertain significance
rs1393276711:149,907,209A/Guncertain significance
rs15537688511:149,907,230T/Cuncertain significance
rs7822148901:149,907,487T/Cuncertain significance
rs7823799241:149,908,085C/Tuncertain significance
rs7819434761:149,908,086G/Auncertain significance
rs2001127451:149,908,100G/Auncertain significance
rs7820536551:149,908,524C/Tuncertain significance
rs20927265101:149,908,534A/Cuncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.