LILRA2
leukocyte immunoglobulin like receptor A2
Summary
This gene encodes a member of a family of immunoreceptors that are expressed predominantly on monocytes and B cells, and at lower levels on dendritic cells and natural killer cells. The encoded protein is an activating receptor that inhibits dendritic cell differentiation and antigen presentation and suppresses innate immune response. Alternatively spliced transcript variants encoding different isoforms have been found. This gene is located in a cluster of related genes on chromosome 19 and there is a pseudogene for this gene on chromosome 3. [provided by RefSeq, Mar 2014]
Known Variants68 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs28384500 | 19:55,084,982 | A/G | upstream gene variant | — |
| rs145704089 | 19:55,085,362 | C/T | — | uncertain significance |
| rs772749570 | 19:55,085,373 | T/C | — | uncertain significance |
| rs139672047 | 19:55,085,376 | C/T | — | uncertain significance |
| rs746905439 | 19:55,085,554 | G/A | — | uncertain significance |
| rs145747345 | 19:55,085,558 | C/T | — | uncertain significance |
| rs185914611 | 19:55,085,569 | G/A | — | uncertain significance |
| rs1834697 | 19:55,085,771 | A/C | — | uncertain significance |
| rs146499061 | 19:55,085,839 | A/G | — | uncertain significance |
| rs774578964 | 19:55,085,852 | G/C | — | likely benign |
| rs764683666 | 19:55,085,911 | C/T | — | uncertain significance |
| rs1489985127 | 19:55,085,918 | A/C | — | uncertain significance |
| rs189159031 | 19:55,085,920 | G/A | — | uncertain significance |
| rs1333563758 | 19:55,085,978 | G/A | — | uncertain significance |
| rs1479534534 | 19:55,085,990 | A/C | — | uncertain significance |
| rs199926951 | 19:55,086,014 | C/T | — | uncertain significance |
| rs76682167 | 19:55,086,139 | C/T | intron variant | — |
| rs372382537 | 19:55,086,235 | C/A | — | uncertain significance |
| rs768895218 | 19:55,086,264 | C/T | — | uncertain significance |
| rs2514098448 | 19:55,086,282 | A/G | — | uncertain significance |
| rs2514098827 | 19:55,086,321 | A/C | — | uncertain significance |
| rs774365077 | 19:55,086,322 | A/T | — | uncertain significance |
| rs112235102 | 19:55,086,339 | G/A | — | uncertain significance |
| rs749102289 | 19:55,086,369 | G/C | — | uncertain significance |
| rs748077295 | 19:55,086,374 | T/C | — | uncertain significance |
| rs754870024 | 19:55,086,404 | C/G | — | uncertain significance |
| rs74454618 | 19:55,086,405 | C/T | — | uncertain significance |
| rs200966581 | 19:55,086,410 | C/T | — | uncertain significance |
| rs145828468 | 19:55,086,422 | T/C | — | uncertain significance |
| rs184492373 | 19:55,086,456 | A/G | — | uncertain significance |
| rs780263633 | 19:55,086,459 | T/A | — | uncertain significance |
| rs752284633 | 19:55,086,478 | T/A | — | uncertain significance |
| rs561216122 | 19:55,086,784 | C/G | — | uncertain significance |
| rs753006012 | 19:55,086,812 | G/A | — | uncertain significance |
| rs895561106 | 19:55,086,815 | T/C | — | uncertain significance |
| rs375220153 | 19:55,086,848 | C/T | — | uncertain significance |
| rs775694135 | 19:55,086,863 | C/T | — | uncertain significance |
| rs151204613 | 19:55,086,864 | G/A | — | uncertain significance |
| rs748202889 | 19:55,086,948 | G/C | — | uncertain significance |
| rs753885831 | 19:55,086,972 | C/T | — | uncertain significance |
| rs143337690 | 19:55,086,982 | G/C | — | uncertain significance |
| rs141524982 | 19:55,086,986 | G/A | — | uncertain significance |
| rs199902538 | 19:55,087,279 | T/A | — | likely benign |
| rs1271059116 | 19:55,087,282 | T/C | — | uncertain significance |
| rs764046844 | 19:55,087,283 | A/G | — | uncertain significance |
| rs1483726350 | 19:55,087,286 | A/G | — | uncertain significance |
| rs568157722 | 19:55,087,349 | T/C | — | uncertain significance |
| rs750521562 | 19:55,087,357 | T/A | — | uncertain significance |
| rs373320838 | 19:55,087,395 | G/T | — | uncertain significance |
| rs145552399 | 19:55,087,399 | G/A | — | uncertain significance |
| rs1241614277 | 19:55,087,439 | C/T | — | uncertain significance |
| rs746918235 | 19:55,087,465 | A/G | — | uncertain significance |
| rs759626170 | 19:55,087,472 | C/T | — | uncertain significance |
| rs75028967 | 19:55,087,490 | T/G | — | uncertain significance |
| rs182749996 | 19:55,087,528 | C/T | — | uncertain significance |
| rs764723529 | 19:55,087,555 | C/T | — | uncertain significance |
| rs549074176 | 19:55,088,477 | C/T | — | — |
| rs547753507 | 19:55,088,717 | G/A | — | — |
| rs117250638 | 19:55,093,336 | G/C | intron variant | — |
| rs74345525 | 19:55,096,748 | T/G | upstream gene variant | — |
| rs755915303 | 19:55,098,488 | A/T | — | uncertain significance |
| rs2241524 | 19:55,098,667 | G/A | splice region variant | — |
| rs2514186949 | 19:55,098,709 | C/A | — | uncertain significance |
| rs774107949 | 19:55,098,805 | G/A | — | likely benign |
| rs112416574 | 19:55,099,976 | G/A | downstream gene variant | — |
| rs78355464 | 19:55,100,262 | T/A | upstream gene variant | — |
| rs12983953 | 19:55,100,418 | C/G | — | — |
| rs272406 | 19:55,100,503 | T/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.