CD82
CD82 molecule
Summary
This metastasis suppressor gene product is a membrane glycoprotein that is a member of the transmembrane 4 superfamily. Expression of this gene has been shown to be downregulated in tumor progression of human cancers and can be activated by p53 through a consensus binding sequence in the promoter. Its expression and that of p53 are strongly correlated, and the loss of expression of these two proteins is associated with poor survival for prostate cancer patients. Two alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs12277292 | 11:44,587,748 | C/G | regulatory region variant | — |
| rs1864297 | 11:44,593,884 | T/A | intron variant | — |
| rs11038065 | 11:44,598,436 | A/T | — | — |
| rs11605647 | 11:44,598,437 | G/A | intron variant | — |
| rs35056404 | 11:44,600,733 | G/A | intron variant | — |
| rs730129 | 11:44,603,328 | A/T | — | — |
| rs148396643 | 11:44,621,739 | T/C | — | uncertain significance |
| rs756411683 | 11:44,621,768 | A/G | — | uncertain significance |
| rs371929631 | 11:44,626,640 | T/C | — | uncertain significance |
| rs34170190 | 11:44,626,657 | G/A | — | benign |
| rs369269460 | 11:44,626,697 | G/A | — | uncertain significance |
| rs202180602 | 11:44,635,558 | G/T | — | — |
| rs2303865 | 11:44,636,833 | G/A | synonymous variant | — |
| rs2540070308 | 11:44,639,767 | T/G | — | uncertain significance |
| rs2540070390 | 11:44,639,790 | C/T | — | uncertain significance |
| rs141597594 | 11:44,639,852 | C/T | — | uncertain significance |
| rs200920132 | 11:44,639,853 | G/A | — | uncertain significance |
| rs749820676 | 11:44,639,857 | C/T | — | uncertain significance |
| rs776479933 | 11:44,639,888 | C/G | — | uncertain significance |
| rs1565097176 | 11:44,640,198 | G/A | — | uncertain significance |
| rs146220817 | 11:44,640,200 | A/G | — | uncertain significance |
| rs2540071663 | 11:44,640,227 | A/C | — | uncertain significance |
| rs1230887505 | 11:44,640,238 | A/G | — | uncertain significance |
| rs79095986 | 11:44,640,246 | C/T | — | benign |
| rs1354362688 | 11:44,640,271 | G/A | — | uncertain significance |
| rs74885383 | 11:44,640,616 | G/C | — | benign |
| rs201405906 | 11:44,640,632 | C/T | — | uncertain significance |
| rs147912305 | 11:44,640,665 | C/T | — | uncertain significance |
| rs201671713 | 11:44,640,666 | C/T | — | uncertain significance |
| rs773237459 | 11:44,640,672 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.