IL1RAP
interleukin 1 receptor accessory protein
Summary
This gene encodes a component of the interleukin 1 receptor complex, which initiates signalling events that result in the activation of interleukin 1-responsive genes. Alternative splicing of this gene results in membrane-bound and soluble isoforms differing in their C-terminus. The ratio of soluble to membrane-bound forms increases during acute-phase induction or stress. [provided by RefSeq, Jul 2018]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs79141302 | 3:190,233,273 | G/A | intron variant | — |
| rs9290936 | 3:190,252,635 | G/T | intron variant | — |
| rs530627643 | 3:190,274,687 | A/C | — | — |
| rs141211213 | 3:190,293,837 | T/C | intron variant | — |
| rs1966468 | 3:190,294,703 | G/A | — | — |
| rs12053868 | 3:190,300,004 | A/G | intron variant | — |
| rs10513854 | 3:190,305,874 | C/T | regulatory region variant | — |
| rs142809548 | 3:190,317,240 | T/A | intron variant | — |
| rs146492458 | 3:190,322,002 | T/C | — | benign |
| rs2474299899 | 3:190,322,070 | C/T | — | uncertain significance |
| rs2474299913 | 3:190,322,073 | G/T | — | uncertain significance |
| rs1577705910 | 3:190,322,077 | G/A | — | likely benign |
| rs1386571220 | 3:190,322,123 | C/T | — | uncertain significance |
| rs777978848 | 3:190,322,190 | C/A | — | uncertain significance |
| rs3796293 | 3:190,332,093 | G/A | intron variant | — |
| rs58711093 | 3:190,335,702 | T/C | intron variant | — |
| rs1381460031 | 3:190,338,068 | G/A | — | uncertain significance |
| rs368254828 | 3:190,338,128 | T/A | — | uncertain significance |
| rs372430202 | 3:190,338,163 | G/A | — | uncertain significance |
| rs2885372 | 3:190,344,871 | C/A | — | — |
| rs756041268 | 3:190,345,166 | G/T | — | uncertain significance |
| rs142665925 | 3:190,345,185 | C/T | — | benign |
| rs561517749 | 3:190,345,748 | C/T | — | — |
| rs6444442 | 3:190,346,060 | A/T | — | — |
| rs1024941 | 3:190,346,658 | T/C | — | — |
| rs1024943 | 3:190,346,702 | T/C | downstream gene variant | — |
| rs1180685636 | 3:190,347,224 | T/C | — | uncertain significance |
| rs148996090 | 3:190,347,247 | A/C | — | benign |
| rs1024948 | 3:190,347,681 | C/A | — | — |
| rs7642797 | 3:190,348,515 | G/A | intron variant | — |
| rs724609 | 3:190,349,078 | G/C | — | — |
| rs56823006 | 3:190,349,670 | A/C | — | — |
| rs4686558 | 3:190,349,888 | A/T | — | — |
| rs7626795 | 3:190,350,461 | A/G | intron variant | — |
| rs4624606 | 3:190,354,246 | A/T | intron variant | — |
| rs143761797 | 3:190,357,970 | C/G | regulatory region variant | — |
| rs759387430 | 3:190,362,037 | T/C | — | uncertain significance |
| rs141817756 | 3:190,362,108 | A/G | — | uncertain significance |
| rs2108855383 | 3:190,362,142 | T/C | — | uncertain significance |
| rs571513293 | 3:190,362,665 | G/C | — | — |
| rs145613403 | 3:190,366,388 | G/C | — | uncertain significance |
| rs116127803 | 3:190,373,856 | G/A | — | benign |
| rs1444026264 | 3:190,373,881 | G/A | — | uncertain significance |
| rs2474500009 | 3:190,373,958 | G/T | — | uncertain significance |
| rs201781727 | 3:190,374,214 | C/T | — | uncertain significance |
| rs74418158 | 3:190,374,230 | A/G | — | benign |
| rs140122538 | 3:190,374,543 | A/C | upstream gene variant | — |
| rs544705382 | 3:190,375,256 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.