MST1

macrophage stimulating 1

Summary

The protein encoded by this gene contains four kringle domains and a serine protease domain, similar to that found in hepatic growth factor. Despite the presence of the serine protease domain, the encoded protein may not have any proteolytic activity. The receptor for this protein is RON tyrosine kinase, which upon activation stimulates ciliary motility of ciliated epithelial lung cells. This protein is secreted and cleaved to form an alpha chain and a beta chain bridged by disulfide bonds. [provided by RefSeq, Jan 2010]

Known Variants62 total

rsidPosition (GRCh37)AllelesClassClinVar
rs25446378113:49,721,466C/T—uncertain significance
rs7781052103:49,721,531C/T—uncertain significance
rs14093909853:49,721,549C/T—uncertain significance
rs7582855823:49,721,577C/T—uncertain significance
rs1415946713:49,721,592T/C—uncertain significance
rs2002686003:49,721,622C/T—uncertain significance
rs1998104033:49,721,797C/G—uncertain significance
rs7741710443:49,721,806G/T—uncertain significance
rs1381557863:49,721,811C/T—uncertain significance
rs1426900323:49,721,812G/A—benign
rs12770302903:49,721,826C/T—uncertain significance
rs25446409493:49,721,863T/G—uncertain significance
rs7612481043:49,722,175C/T—uncertain significance
rs13025114803:49,722,186A/G—uncertain significance
rs2004927323:49,722,292C/T—uncertain significance
rs7606560293:49,722,464G/A—uncertain significance
rs3754388383:49,722,701C/T—uncertain significance
rs1491383923:49,722,706G/A—likely benign
rs1423448383:49,722,759A/G—uncertain significance
rs1492555163:49,722,765G/A—conflicting classifications of pathogenicity
rs25446488773:49,722,779T/C—uncertain significance
rs1380409543:49,722,795A/G—uncertain significance
rs7740156943:49,722,910G/A—uncertain significance
rs5451622533:49,722,911G/T—likely benign
rs3682827603:49,722,922A/G—uncertain significance
rs7573869563:49,723,061G/A—uncertain significance
rs3746270793:49,723,073A/G—likely benign
rs12231541863:49,723,076G/A—uncertain significance
rs7463685943:49,723,099A/G—likely benign
rs5288938153:49,723,116G/A—uncertain significance
rs622626833:49,723,147T/Csynonymous variant—
rs7743515853:49,723,317G/A—uncertain significance
rs1490865663:49,723,376C/T—likely benign
rs12649494463:49,723,384C/A—uncertain significance
rs20537063863:49,723,503C/T—uncertain significance
rs3733267653:49,723,518C/T—uncertain significance
rs7740265283:49,723,521C/G—uncertain significance
rs7518089183:49,723,548C/T—uncertain significance
rs25446578193:49,723,579G/A—uncertain significance
rs7749192053:49,723,602C/T—uncertain significance
rs25446613233:49,723,770A/T—uncertain significance
rs97136513:49,723,784C/A—likely benign
rs74312153:49,723,823A/G—likely benign
rs5616155223:49,723,845C/T—uncertain significance
rs7533548673:49,723,855C/T—uncertain significance
rs3754227023:49,723,859C/A—uncertain significance
rs7615822213:49,723,913C/A—likely benign
rs1488053293:49,724,465C/G—benign
rs7804764263:49,724,686T/C—uncertain significance
rs14773990273:49,724,799G/C—uncertain significance
rs20538653223:49,724,813A/G—uncertain significance
rs11598731663:49,724,903G/C—uncertain significance
rs7457297453:49,725,009C/T—uncertain significance
rs12924970223:49,725,043A/G—uncertain significance
rs3738905763:49,725,207C/T—uncertain significance
rs2011393833:49,725,234A/C—uncertain significance
rs7815051693:49,725,253C/T—uncertain significance
rs14371245403:49,725,267T/A—uncertain significance
rs7525723653:49,725,294C/T—uncertain significance
rs622626863:49,726,070G/A—uncertain significance
rs12815014523:49,726,103C/T—uncertain significance
rs25446806833:49,726,114C/G—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.