VSTM4
V-set and transmembrane domain containing 4
Summary
Predicted to act upstream of or within several processes, including endothelial cell proliferation; retina blood vessel maintenance; and vasculature development. Predicted to be located in extracellular region and plasma membrane. Predicted to be active in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2244967 | 10:50,224,766 | C/A | — | — |
| rs777532823 | 10:50,227,704 | G/C | — | uncertain significance |
| rs1843152131 | 10:50,227,745 | G/T | — | uncertain significance |
| rs1420463447 | 10:50,227,763 | G/A | — | uncertain significance |
| rs375569682 | 10:50,227,796 | T/C | — | uncertain significance |
| rs2494654373 | 10:50,227,802 | T/A | — | uncertain significance |
| rs2137920 | 10:50,229,638 | T/A | downstream gene variant | — |
| rs61850684 | 10:50,252,936 | G/A | intron variant | — |
| rs371290102 | 10:50,255,032 | G/A | — | uncertain significance |
| rs187843947 | 10:50,255,086 | G/A | — | uncertain significance |
| rs761253049 | 10:50,256,532 | G/T | — | uncertain significance |
| rs753977306 | 10:50,256,538 | C/T | — | uncertain significance |
| rs1206080029 | 10:50,256,567 | C/T | — | uncertain significance |
| rs769792534 | 10:50,256,582 | G/A | — | uncertain significance |
| rs17011715 | 10:50,261,777 | T/G | regulatory region variant | — |
| rs56157539 | 10:50,261,880 | C/T | regulatory region variant | — |
| rs17011726 | 10:50,264,204 | C/G | intron variant | — |
| rs4264085 | 10:50,264,963 | T/G | — | — |
| rs36116147 | 10:50,266,930 | G/T | intron variant | — |
| rs61850693 | 10:50,269,487 | T/G | intron variant | — |
| rs74939581 | 10:50,282,229 | A/T | — | — |
| rs61848377 | 10:50,283,092 | G/A | intron variant | — |
| rs1218593460 | 10:50,285,359 | T/C | — | uncertain significance |
| rs1564585153 | 10:50,285,363 | C/T | — | likely benign |
| rs12257242 | 10:50,291,400 | C/G | intron variant | — |
| rs4240499 | 10:50,310,251 | T/C | intron variant | — |
| rs145294709 | 10:50,315,720 | C/T | — | uncertain significance |
| rs142283092 | 10:50,315,729 | C/G | — | uncertain significance |
| rs1424967763 | 10:50,315,740 | G/A | — | uncertain significance |
| rs138812288 | 10:50,315,780 | G/A | — | uncertain significance |
| rs563816877 | 10:50,315,821 | C/A | — | uncertain significance |
| rs867284678 | 10:50,315,842 | T/A | — | uncertain significance |
| rs34832077 | 10:50,315,846 | C/T | — | uncertain significance |
| rs370616319 | 10:50,315,954 | C/T | — | uncertain significance |
| rs149754840 | 10:50,316,031 | G/A | — | uncertain significance |
| rs1394107294 | 10:50,316,038 | C/A | — | uncertain significance |
| rs4073711 | 10:50,317,651 | A/G | intron variant | — |
| rs1844979331 | 10:50,323,503 | C/T | — | uncertain significance |
| rs751197008 | 10:50,323,508 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.