VCAM1
vascular cell adhesion molecule 1
Summary
This gene is a member of the Ig superfamily and encodes a cell surface sialoglycoprotein expressed by cytokine-activated endothelium. This type I membrane protein mediates leukocyte-endothelial cell adhesion and signal transduction, and may play a role in the development of artherosclerosis and rheumatoid arthritis. Three alternatively spliced transcripts encoding different isoforms have been described for this gene. [provided by RefSeq, Dec 2010]
Known Variants46 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1041163 | 1:101,183,825 | T/C | upstream gene variant | — |
| rs3783605 | 1:101,184,877 | A/G | upstream gene variant | — |
| rs1659891136 | 1:101,185,441 | C/T | — | likely benign |
| rs148280495 | 1:101,185,447 | G/A | — | uncertain significance |
| rs144133931 | 1:101,185,453 | A/T | — | uncertain significance |
| rs368309387 | 1:101,186,074 | T/G | — | uncertain significance |
| rs145509462 | 1:101,186,084 | T/C | — | likely benign |
| rs754424141 | 1:101,186,182 | C/T | — | uncertain significance |
| rs142501320 | 1:101,186,203 | C/T | — | uncertain significance |
| rs900346086 | 1:101,186,205 | C/G | — | uncertain significance |
| rs3176861 | 1:101,187,321 | C/T | regulatory region variant | — |
| rs369833640 | 1:101,188,567 | C/T | — | likely benign |
| rs2524021422 | 1:101,188,621 | C/T | — | likely benign |
| rs755932839 | 1:101,188,704 | C/A | — | uncertain significance |
| rs748417631 | 1:101,188,737 | G/A | — | uncertain significance |
| rs139874936 | 1:101,188,746 | A/G | — | uncertain significance |
| rs767446399 | 1:101,188,812 | C/A | — | uncertain significance |
| rs201542521 | 1:101,188,849 | A/G | — | uncertain significance |
| rs753463883 | 1:101,190,259 | C/T | — | likely benign |
| rs754644270 | 1:101,190,262 | C/T | — | likely benign |
| rs2524028591 | 1:101,190,299 | A/C | — | uncertain significance |
| rs142673263 | 1:101,190,315 | A/C | — | uncertain significance |
| rs775533364 | 1:101,190,417 | A/G | — | uncertain significance |
| rs2524029171 | 1:101,190,420 | G/A | — | uncertain significance |
| rs3917010 | 1:101,190,866 | A/C | intron variant | — |
| rs758576380 | 1:101,194,683 | A/G | — | uncertain significance |
| rs778041376 | 1:101,194,744 | T/C | — | uncertain significance |
| rs147743071 | 1:101,194,746 | A/G | — | uncertain significance |
| rs1327695769 | 1:101,194,929 | G/C | — | uncertain significance |
| rs757039798 | 1:101,196,760 | C/G | — | uncertain significance |
| rs3783613 | 1:101,196,787 | G/C | missense variant | — |
| rs34199378 | 1:101,197,012 | A/G | — | benign |
| rs2524051819 | 1:101,197,057 | A/G | — | uncertain significance |
| rs200949878 | 1:101,198,105 | G/A | — | uncertain significance |
| rs1571460918 | 1:101,198,113 | A/G | — | likely benign |
| rs2524057408 | 1:101,198,136 | C/T | — | uncertain significance |
| rs1207315091 | 1:101,198,141 | A/G | — | uncertain significance |
| rs368917883 | 1:101,198,205 | G/A | — | uncertain significance |
| rs769161166 | 1:101,200,100 | G/C | — | uncertain significance |
| rs1660585480 | 1:101,200,211 | T/C | — | likely benign |
| rs777392031 | 1:101,200,253 | C/G | — | uncertain significance |
| rs138060304 | 1:101,203,691 | A/G | — | uncertain significance |
| rs758782913 | 1:101,203,705 | T/G | — | uncertain significance |
| rs747347841 | 1:101,203,717 | C/G | — | uncertain significance |
| rs1396084606 | 1:101,203,769 | T/G | — | uncertain significance |
| rs764677426 | 1:101,203,798 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.