JAM2
junctional adhesion molecule 2
Summary
This gene belongs to the immunoglobulin superfamily, and the junctional adhesion molecule (JAM) family. The protein encoded by this gene is a type I membrane protein that is localized at the tight junctions of both epithelial and endothelial cells. It acts as an adhesive ligand for interacting with a variety of immune cell types, and may play a role in lymphocyte homing to secondary lymphoid organs. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jul 2012]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs145504626 | 21:27,011,458 | T/A | — | benign |
| rs118115569 | 21:27,012,088 | C/A | — | benign |
| rs1600978441 | 21:27,012,134 | A/G | — | pathogenic |
| rs8132639 | 21:27,012,154 | C/A | — | benign |
| rs1473673314 | 21:27,012,198 | G/A | — | uncertain significance |
| rs2829841 | 21:27,023,022 | C/T | intron variant | — |
| rs28507219 | 21:27,047,662 | A/T | — | — |
| rs2829863 | 21:27,056,099 | A/C | — | benign |
| rs754402473 | 21:27,056,246 | C/T | — | uncertain significance |
| rs8133602 | 21:27,056,250 | A/G | — | benign |
| rs2829866 | 21:27,059,071 | T/A | intron variant | — |
| rs9984260 | 21:27,065,860 | T/C | — | benign |
| rs61140678 | 21:27,065,919 | A/G | — | benign |
| rs2516791219 | 21:27,066,089 | A/C | — | uncertain significance |
| rs1383641309 | 21:27,066,149 | G/A | — | pathogenic |
| rs9982750 | 21:27,071,005 | A/G | — | benign |
| rs200962285 | 21:27,071,018 | C/A | — | uncertain significance |
| rs767188712 | 21:27,071,069 | G/C | — | uncertain significance |
| rs1230941179 | 21:27,071,098 | G/C | — | pathogenic |
| rs2123399043 | 21:27,071,112 | T/C | — | uncertain significance |
| rs780217409 | 21:27,071,115 | G/A | — | uncertain significance |
| rs2516802140 | 21:27,074,490 | T/C | — | likely benign |
| rs753604532 | 21:27,074,534 | G/A | — | uncertain significance |
| rs2516802255 | 21:27,074,536 | A/G | — | uncertain significance |
| rs781261918 | 21:27,074,569 | C/T | — | pathogenic |
| rs145881376 | 21:27,074,574 | G/C | — | uncertain significance |
| rs73335965 | 21:27,074,708 | C/T | — | benign |
| rs2276220 | 21:27,078,270 | G/A | — | benign |
| rs7277917 | 21:27,078,296 | C/T | — | uncertain significance |
| rs200218663 | 21:27,078,323 | G/A | — | uncertain significance |
| rs2516806548 | 21:27,078,324 | T/C | — | uncertain significance |
| rs370187720 | 21:27,078,350 | G/A | — | uncertain significance |
| rs371009159 | 21:27,078,362 | G/A | — | uncertain significance |
| rs2829870 | 21:27,078,428 | T/A | — | benign |
| rs2026224 | 21:27,078,633 | G/A | — | benign |
| rs56256482 | 21:27,081,725 | T/G | — | benign |
| rs7276129 | 21:27,081,942 | A/G | — | benign |
| rs2516813833 | 21:27,084,653 | A/G | — | uncertain significance |
| rs9976382 | 21:27,084,686 | A/C | — | benign |
| rs8134487 | 21:27,086,850 | C/T | — | benign |
| rs8134513 | 21:27,086,916 | C/A | — | benign |
| rs2829877 | 21:27,087,044 | T/C | — | benign |
| rs2829878 | 21:27,087,165 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.