IL1RL2
interleukin 1 receptor like 2
Summary
The protein encoded by this gene is a member of the interleukin 1 receptor family. An experiment with transient gene expression demonstrated that this receptor was incapable of binding to interleukin 1 alpha and interleukin 1 beta with high affinity. This gene and four other interleukin 1 receptor family genes, including interleukin 1 receptor, type I (IL1R1), interleukin 1 receptor, type II (IL1R2), interleukin 1 receptor-like 1 (IL1RL1), and interleukin 18 receptor 1 (IL18R1), form a cytokine receptor gene cluster in a region mapped to chromosome 2q12. [provided by RefSeq, Jul 2008]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2241132 | 2:102,804,035 | C/A | — | association |
| rs1997504 | 2:102,804,831 | T/G | — | — |
| rs535165337 | 2:102,805,563 | A/T | — | uncertain significance |
| rs776005558 | 2:102,805,602 | G/A | — | uncertain significance |
| rs753834474 | 2:102,805,730 | A/G | — | uncertain significance |
| rs2528743033 | 2:102,805,734 | A/T | — | uncertain significance |
| rs765151788 | 2:102,805,745 | T/A | — | uncertain significance |
| rs778363198 | 2:102,808,456 | T/C | — | uncertain significance |
| rs2528765827 | 2:102,808,528 | G/T | — | uncertain significance |
| rs1202931052 | 2:102,808,564 | C/A | — | uncertain significance |
| rs1558648 | 2:102,810,168 | T/G | intron variant | — |
| rs190473555 | 2:102,822,946 | T/C | intron variant | — |
| rs138307764 | 2:102,824,159 | G/T | intron variant | — |
| rs186799902 | 2:102,824,973 | A/G | intron variant | — |
| rs148020709 | 2:102,825,063 | G/A | intron variant | — |
| rs190476496 | 2:102,825,687 | T/A | intron variant | — |
| rs13405631 | 2:102,828,620 | T/C | — | benign |
| rs1922291 | 2:102,828,817 | A/G | intron variant | — |
| rs6743219 | 2:102,831,711 | T/C | intron variant | — |
| rs538428003 | 2:102,835,048 | C/A | — | — |
| rs2528963345 | 2:102,835,481 | G/T | — | uncertain significance |
| rs1282187332 | 2:102,835,488 | A/G | — | uncertain significance |
| rs1374697023 | 2:102,835,534 | A/C | — | uncertain significance |
| rs150558280 | 2:102,836,357 | C/T | — | uncertain significance |
| rs375407590 | 2:102,836,367 | A/G | — | uncertain significance |
| rs1030393446 | 2:102,836,390 | T/C | — | uncertain significance |
| rs751284150 | 2:102,836,405 | A/T | — | uncertain significance |
| rs368189171 | 2:102,836,407 | G/T | — | uncertain significance |
| rs140532168 | 2:102,836,463 | T/C | — | uncertain significance |
| rs34376156 | 2:102,841,090 | T/G | intron variant | — |
| rs745947339 | 2:102,842,361 | C/T | — | uncertain significance |
| rs946791842 | 2:102,842,387 | G/A | — | uncertain significance |
| rs539319037 | 2:102,842,396 | G/A | — | uncertain significance |
| rs33946385 | 2:102,842,420 | G/A | — | benign |
| rs751858304 | 2:102,842,421 | T/C | — | uncertain significance |
| rs138105991 | 2:102,842,430 | T/C | missense variant | — |
| rs1690573653 | 2:102,842,435 | A/C | — | uncertain significance |
| rs1029536633 | 2:102,842,493 | C/A | — | uncertain significance |
| rs186980156 | 2:102,842,559 | C/A | intron variant | — |
| rs113857898 | 2:102,847,271 | G/C | intron variant | — |
| rs759788405 | 2:102,849,500 | G/A | — | uncertain significance |
| rs149853964 | 2:102,851,075 | C/T | intron variant | — |
| rs951341852 | 2:102,851,357 | C/T | — | uncertain significance |
| rs370451497 | 2:102,851,365 | A/G | — | uncertain significance |
| rs778637368 | 2:102,851,383 | G/A | — | likely benign |
| rs761435720 | 2:102,851,411 | T/C | — | uncertain significance |
| rs998938997 | 2:102,851,413 | G/T | — | likely benign |
| rs75091099 | 2:102,851,470 | G/T | missense variant | — |
| rs752467081 | 2:102,851,538 | C/G | — | uncertain significance |
| rs2529068377 | 2:102,851,581 | C/T | — | uncertain significance |
| rs111997166 | 2:102,851,588 | C/T | — | likely benign |
| rs373785659 | 2:102,851,612 | C/G | — | uncertain significance |
| rs1674757999 | 2:102,851,631 | G/A | — | uncertain significance |
| rs200652363 | 2:102,851,669 | C/T | — | uncertain significance |
| rs141789680 | 2:102,851,670 | G/T | — | likely benign |
| rs2302612 | 2:102,851,708 | T/C | missense variant | — |
| rs139406977 | 2:102,851,724 | C/T | — | likely benign |
| rs10167431 | 2:102,852,802 | T/C | — | association |
Gene information from NCBI Gene. Variant classifications from ClinVar.