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
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs150241335 | 17:26,694,432 | G/A | — | likely benign |
| rs994071377 | 17:26,694,445 | T/C | — | uncertain significance |
| rs2508150837 | 17:26,694,452 | G/A | — | uncertain significance |
| rs781890691 | 17:26,694,461 | T/C | — | likely benign |
| rs1755772052 | 17:26,694,476 | T/A | — | uncertain significance |
| rs2227728 | 17:26,694,483 | A/G | — | benign |
| rs3211344 | 17:26,694,746 | G/T | — | uncertain significance |
| rs111707768 | 17:26,694,793 | C/T | — | uncertain significance |
| rs2508152084 | 17:26,694,798 | C/T | — | uncertain significance |
| rs704 | 17:26,694,861 | G/A | — | benign |
| rs1555583248 | 17:26,694,864 | G/A | — | uncertain significance |
| rs782476690 | 17:26,694,865 | C/T | — | uncertain significance |
| rs368991682 | 17:26,694,877 | G/A | — | uncertain significance |
| rs916657 | 17:26,694,890 | G/A | — | benign |
| rs150566083 | 17:26,694,894 | C/T | — | uncertain significance |
| rs139553576 | 17:26,694,903 | C/T | — | uncertain significance |
| rs902942336 | 17:26,694,979 | G/C | — | uncertain significance |
| rs782797163 | 17:26,695,010 | C/A | — | uncertain significance |
| rs2508153345 | 17:26,695,038 | C/T | — | uncertain significance |
| rs374231917 | 17:26,695,040 | G/A | — | likely benign |
| rs782484700 | 17:26,695,044 | C/G | — | uncertain significance |
| rs554136380 | 17:26,695,051 | G/A | — | uncertain significance |
| rs377647331 | 17:26,695,054 | T/C | — | uncertain significance |
| rs782306878 | 17:26,695,084 | T/C | — | likely benign |
| rs142651994 | 17:26,695,549 | T/A | — | uncertain significance |
| rs143380142 | 17:26,695,573 | G/C | — | uncertain significance |
| rs527927776 | 17:26,695,625 | G/A | — | uncertain significance |
| rs34134929 | 17:26,695,630 | G/A | — | benign |
| rs2508155488 | 17:26,695,689 | G/C | — | uncertain significance |
| rs2227725 | 17:26,695,704 | A/G | — | benign |
| rs782375556 | 17:26,695,896 | T/G | — | uncertain significance |
| rs2227723 | 17:26,695,916 | C/T | — | benign |
| rs564459012 | 17:26,695,917 | G/C | — | uncertain significance |
| rs1467657435 | 17:26,695,923 | T/A | — | uncertain significance |
| rs782268632 | 17:26,696,033 | C/T | — | uncertain significance |
| rs781978849 | 17:26,696,043 | G/C | — | uncertain significance |
| rs2508157704 | 17:26,696,338 | T/A | — | uncertain significance |
| rs782356682 | 17:26,696,345 | G/A | — | uncertain significance |
| rs201871756 | 17:26,696,354 | C/T | — | uncertain significance |
| rs371982238 | 17:26,696,379 | C/G | — | uncertain significance |
| rs782369755 | 17:26,696,444 | A/G | — | uncertain significance |
| rs35339100 | 17:26,696,550 | G/A | — | benign |
| rs1044296654 | 17:26,696,563 | G/T | — | uncertain significance |
| rs782820530 | 17:26,696,570 | C/T | — | uncertain significance |
| rs373650198 | 17:26,696,571 | G/A | — | likely benign |
| rs782222213 | 17:26,696,613 | C/T | — | likely benign |
| rs112887300 | 17:26,696,680 | T/A | — | conflicting classifications of pathogenicity |
| rs144093348 | 17:26,696,686 | G/A | — | uncertain significance |
| rs2508159348 | 17:26,696,764 | A/G | — | likely benign |
| rs367756510 | 17:26,696,768 | A/G | — | uncertain significance |
| rs145095194 | 17:26,696,866 | C/T | — | uncertain significance |
| rs782022688 | 17:26,696,877 | A/G | — | likely benign |
| rs140248417 | 17:26,696,988 | C/G | — | uncertain significance |
| rs111490653 | 17:26,697,009 | G/A | — | benign |
| rs145861745 | 17:26,697,033 | G/A | — | likely benign |
| rs376564388 | 17:26,697,152 | C/A | — | likely benign |
| rs148994005 | 17:26,697,164 | G/C | — | uncertain significance |
| rs2227721 | 17:26,697,451 | C/A | regulatory region variant | — |
| rs2227720 | 17:26,697,521 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.