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

Gene information from NCBI Gene. Variant classifications from ClinVar.