VTN

vitronectin

Summary

The protein encoded by this gene functions in part as an adhesive glycoprotein. Differential expression of this protein can promote either cell adhesion or migration as it links cells to the extracellular matrix through a variety of ligands. These ligands include integrins, plasminogen activator inhibitor-1, and urokinase plasminogen activator receptor. This secreted protein can be present in the plasma as a monomer or dimer and forms a multimer in the extracellular matrix of several tissues. This protein also inhibits the membrane-damaging effect of the terminal cytolytic complement pathway and binds to several serpin serine protease inhibitors. This protein can also promote extracellular matrix degradation and thus plays a role in tumorigenesis. It is involved in a variety of other biological processes such as the regulation of the coagulation pathway, wound healing, and tissue remodeling. The heparin-binding domain of this protein give it anti-microbial properties. It is also a lipid binding protein that forms a principal component of high density lipoprotein. [provided by RefSeq, Aug 2020]

Known Variants59 total

rsidPosition (GRCh37)AllelesClassClinVar
rs15024133517:26,694,432G/Alikely benign
rs99407137717:26,694,445T/Cuncertain significance
rs250815083717:26,694,452G/Auncertain significance
rs78189069117:26,694,461T/Clikely benign
rs175577205217:26,694,476T/Auncertain significance
rs222772817:26,694,483A/Gbenign
rs321134417:26,694,746G/Tuncertain significance
rs11170776817:26,694,793C/Tuncertain significance
rs250815208417:26,694,798C/Tuncertain significance
rs70417:26,694,861G/Abenign
rs155558324817:26,694,864G/Auncertain significance
rs78247669017:26,694,865C/Tuncertain significance
rs36899168217:26,694,877G/Auncertain significance
rs91665717:26,694,890G/Abenign
rs15056608317:26,694,894C/Tuncertain significance
rs13955357617:26,694,903C/Tuncertain significance
rs90294233617:26,694,979G/Cuncertain significance
rs78279716317:26,695,010C/Auncertain significance
rs250815334517:26,695,038C/Tuncertain significance
rs37423191717:26,695,040G/Alikely benign
rs78248470017:26,695,044C/Guncertain significance
rs55413638017:26,695,051G/Auncertain significance
rs37764733117:26,695,054T/Cuncertain significance
rs78230687817:26,695,084T/Clikely benign
rs14265199417:26,695,549T/Auncertain significance
rs14338014217:26,695,573G/Cuncertain significance
rs52792777617:26,695,625G/Auncertain significance
rs3413492917:26,695,630G/Abenign
rs250815548817:26,695,689G/Cuncertain significance
rs222772517:26,695,704A/Gbenign
rs78237555617:26,695,896T/Guncertain significance
rs222772317:26,695,916C/Tbenign
rs56445901217:26,695,917G/Cuncertain significance
rs146765743517:26,695,923T/Auncertain significance
rs78226863217:26,696,033C/Tuncertain significance
rs78197884917:26,696,043G/Cuncertain significance
rs250815770417:26,696,338T/Auncertain significance
rs78235668217:26,696,345G/Auncertain significance
rs20187175617:26,696,354C/Tuncertain significance
rs37198223817:26,696,379C/Guncertain significance
rs78236975517:26,696,444A/Guncertain significance
rs3533910017:26,696,550G/Abenign
rs104429665417:26,696,563G/Tuncertain significance
rs78282053017:26,696,570C/Tuncertain significance
rs37365019817:26,696,571G/Alikely benign
rs78222221317:26,696,613C/Tlikely benign
rs11288730017:26,696,680T/Aconflicting classifications of pathogenicity
rs14409334817:26,696,686G/Auncertain significance
rs250815934817:26,696,764A/Glikely benign
rs36775651017:26,696,768A/Guncertain significance
rs14509519417:26,696,866C/Tuncertain significance
rs78202268817:26,696,877A/Glikely benign
rs14024841717:26,696,988C/Guncertain significance
rs11149065317:26,697,009G/Abenign
rs14586174517:26,697,033G/Alikely benign
rs37656438817:26,697,152C/Alikely benign
rs14899400517:26,697,164G/Cuncertain significance
rs222772117:26,697,451C/Aregulatory region variant
rs222772017:26,697,521A/Gregulatory region variant

Gene information from NCBI Gene. Variant classifications from ClinVar.