OTOP3

otopetrin 3

Summary

Predicted to enable identical protein binding activity and proton channel activity. Predicted to be involved in proton transmembrane transport. Predicted to be located in plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants68 total

rsidPosition (GRCh37)AllelesClassClinVar
rs36836709817:72,931,898T/C—likely benign
rs99058838617:72,931,938G/T—uncertain significance
rs142583454017:72,931,951C/T—uncertain significance
rs146137382917:72,931,973G/T—uncertain significance
rs78095779517:72,931,985C/T—uncertain significance
rs138851117:72,935,809T/G——
rs52981133417:72,937,545C/T—uncertain significance
rs36815555917:72,937,568G/A—likely benign
rs36959178117:72,937,577G/A—likely benign
rs116859606117:72,937,593C/T—uncertain significance
rs74595824917:72,937,647G/A—uncertain significance
rs101530688917:72,937,655C/T—uncertain significance
rs76257419417:72,937,674G/A—uncertain significance
rs56786471217:72,937,677A/G—uncertain significance
rs54615537117:72,937,727T/G—uncertain significance
rs105251752317:72,937,736A/T—uncertain significance
rs57347345217:72,937,760G/A—likely benign
rs7284451917:72,937,795G/A—likely benign
rs119676680317:72,937,820C/T—uncertain significance
rs77144123217:72,937,830A/G—uncertain significance
rs254445676217:72,937,832G/A—uncertain significance
rs76828810617:72,937,842C/G—uncertain significance
rs14076759517:72,937,856C/G—uncertain significance
rs203917771717:72,937,890C/G—uncertain significance
rs37702076417:72,937,897G/C—uncertain significance
rs76443216617:72,937,902G/A—uncertain significance
rs75189934117:72,938,019T/C—uncertain significance
rs20024497517:72,938,044G/A—uncertain significance
rs77113033617:72,938,071G/T—uncertain significance
rs6208632117:72,938,108C/G—uncertain significance
rs56341215217:72,938,127G/A—likely benign
rs37770530617:72,939,417C/T—uncertain significance
rs37456823217:72,939,701G/A—likely benign
rs203919880917:72,939,757C/A—uncertain significance
rs75520909017:72,939,775G/A—uncertain significance
rs20106001117:72,939,796G/A—uncertain significance
rs14864264017:72,942,809C/T—uncertain significance
rs95551159517:72,942,827C/T—uncertain significance
rs75097661417:72,942,882T/C—uncertain significance
rs14209402817:72,942,893G/A—uncertain significance
rs37049956717:72,942,900G/A—uncertain significance
rs14138537117:72,942,905G/A—uncertain significance
rs14698121017:72,942,926C/T—uncertain significance
rs75443944617:72,942,942C/G—uncertain significance
rs37663633117:72,942,956G/A—uncertain significance
rs15040882417:72,942,966T/C—uncertain significance
rs130230763817:72,942,972C/T—likely benign
rs13812243617:72,942,981G/T—uncertain significance
rs118957955617:72,943,145C/G—uncertain significance
rs20034474817:72,943,155G/A—uncertain significance
rs13886490117:72,943,179C/T—uncertain significance
rs14218356417:72,943,184C/T—uncertain significance
rs14635909617:72,943,215C/G—uncertain significance
rs74627127017:72,943,235A/G—uncertain significance
rs37297815117:72,943,238G/A—uncertain significance
rs77676956817:72,943,266C/G—uncertain significance
rs76738193917:72,943,271C/T—uncertain significance
rs54832176717:72,943,275C/T—uncertain significance
rs76529141817:72,943,337G/A—likely benign
rs203923790917:72,943,355A/G—uncertain significance
rs77050939217:72,943,373C/T—uncertain significance
rs20153205817:72,943,374G/A—uncertain significance
rs254446264117:72,943,400G/A—uncertain significance
rs53610468717:72,943,520C/T—uncertain significance
rs146571868717:72,943,566T/C—uncertain significance
rs77706544217:72,945,341C/G—uncertain significance
rs7882688617:72,945,385C/T—likely benign
rs37220833117:72,945,465G/A—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.