RASSF5

Ras association domain family member 5

Summary

This gene is a member of the Ras association domain family. It functions as a tumor suppressor, and is inactivated in a variety of cancers. The encoded protein localizes to centrosomes and microtubules, and associates with the GTP-activated forms of Ras, Rap1, and several other Ras-like small GTPases. The protein regulates lymphocyte adhesion and suppresses cell growth in response to activated Rap1 or Ras. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Known Variants29 total

rsidPosition (GRCh37)AllelesClassClinVar
rs66688831:206,679,023T/Aupstream gene variant—
rs15533939691:206,681,029G/C—uncertain significance
rs16664921041:206,681,045C/T—uncertain significance
rs15533939781:206,681,047C/G—uncertain significance
rs7823270601:206,681,065C/T—uncertain significance
rs5771324001:206,681,069G/T—uncertain significance
rs8885162231:206,681,075C/T—uncertain significance
rs25289785981:206,681,080C/A—uncertain significance
rs7823347421:206,681,095C/T—uncertain significance
rs7821194881:206,681,102C/G—uncertain significance
rs7820244541:206,681,113C/G—uncertain significance
rs10067064601:206,681,119G/A—uncertain significance
rs5619188831:206,681,137G/T—uncertain significance
rs7818981981:206,681,173G/A—uncertain significance
rs7825423151:206,681,176C/G—uncertain significance
rs7823327741:206,681,279T/G—uncertain significance
rs7827993841:206,711,530C/T—uncertain significance
rs7827629211:206,711,535C/G—uncertain significance
rs7826388291:206,711,576G/A—uncertain significance
rs5481101441:206,715,627A/G——
rs2000769131:206,756,683G/A—uncertain significance
rs10466889401:206,757,846C/T—uncertain significance
rs7823162661:206,757,992A/G—uncertain significance
rs5700393541:206,757,996G/A—uncertain significance
rs16690330861:206,757,998A/T—uncertain significance
rs7823122711:206,758,542G/A—uncertain significance
rs7822926081:206,758,574G/A—uncertain significance
rs12534441231:206,758,620A/C—uncertain significance
rs7648444741:206,760,221G/C—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.