IRAK1
interleukin 1 receptor associated kinase 1
Summary
This gene encodes the interleukin-1 receptor-associated kinase 1, one of two putative serine/threonine kinases that become associated with the interleukin-1 receptor (IL1R) upon stimulation. This gene is partially responsible for IL1-induced upregulation of the transcription factor NF-kappa B. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants62 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs3027898 | X:153,275,890 | C/G | — | — |
| rs375975243 | X:153,277,362 | C/T | — | uncertain significance |
| rs2239673 | X:153,277,889 | C/T | — | benign |
| rs149773870 | X:153,277,986 | G/C | — | uncertain significance |
| rs147444875 | X:153,277,988 | G/A | — | uncertain significance |
| rs782722759 | X:153,278,057 | T/C | — | uncertain significance |
| rs145414165 | X:153,278,500 | C/T | — | uncertain significance |
| rs35638718 | X:153,278,550 | G/A | — | benign |
| rs34112487 | X:153,278,569 | C/T | — | likely benign |
| rs1557127993 | X:153,278,601 | C/A | — | uncertain significance |
| rs782780153 | X:153,278,625 | C/T | — | benign |
| rs199501854 | X:153,278,626 | G/A | — | uncertain significance |
| rs3027905 | X:153,278,723 | T/C | — | likely benign |
| rs782687454 | X:153,278,743 | A/G | — | uncertain significance |
| rs782284654 | X:153,278,752 | C/T | — | uncertain significance |
| rs140583367 | X:153,278,782 | C/T | — | likely benign |
| rs782393640 | X:153,278,783 | G/A | — | likely benign |
| rs1059703 | X:153,278,829 | G/A | missense variant | benign |
| rs368063747 | X:153,278,836 | C/T | — | uncertain significance |
| rs782357859 | X:153,279,560 | A/G | — | uncertain significance |
| rs2521924158 | X:153,279,569 | T/C | — | uncertain significance |
| rs2065722135 | X:153,279,572 | G/C | — | uncertain significance |
| rs2065722170 | X:153,279,573 | G/C | — | uncertain significance |
| rs782315247 | X:153,279,615 | T/A | — | uncertain significance |
| rs782373597 | X:153,279,624 | C/T | — | uncertain significance |
| rs2065723451 | X:153,279,731 | T/C | — | uncertain significance |
| rs5945174 | X:153,279,858 | G/C | — | — |
| rs2521931038 | X:153,281,491 | T/C | — | uncertain significance |
| rs782768715 | X:153,281,508 | G/A | — | likely benign |
| rs1229790473 | X:153,281,929 | C/G | — | uncertain significance |
| rs782053956 | X:153,281,984 | C/T | — | likely benign |
| rs2521933469 | X:153,281,986 | G/A | — | uncertain significance |
| rs202203227 | X:153,281,996 | G/A | — | likely benign |
| rs11556424 | X:153,282,020 | G/A | — | benign |
| rs149520139 | X:153,282,026 | G/A | — | likely benign |
| rs143993525 | X:153,282,028 | G/A | — | likely benign |
| rs2065752119 | X:153,283,448 | T/C | — | likely benign |
| rs1194250023 | X:153,283,462 | A/T | — | uncertain significance |
| rs781836564 | X:153,283,522 | C/T | — | uncertain significance |
| rs1557130061 | X:153,283,744 | G/T | — | likely benign |
| rs368268634 | X:153,284,040 | C/T | — | likely benign |
| rs782263874 | X:153,284,053 | C/T | — | likely benign |
| rs782106693 | X:153,284,140 | C/T | — | likely benign |
| rs2521943549 | X:153,284,151 | G/A | — | uncertain significance |
| rs10127175 | X:153,284,172 | A/T | — | benign |
| rs1059702 | X:153,284,192 | A/G | missense variant | benign |
| rs11465830 | X:153,284,198 | C/T | — | benign |
| rs782216618 | X:153,284,428 | T/G | — | uncertain significance |
| rs202066173 | X:153,284,436 | G/A | — | conflicting classifications of pathogenicity |
| rs2521945482 | X:153,284,442 | G/T | — | uncertain significance |
| rs782295969 | X:153,284,472 | G/A | — | uncertain significance |
| rs1059701 | X:153,284,483 | G/A | — | benign |
| rs782338967 | X:153,284,490 | C/T | — | uncertain significance |
| rs782422452 | X:153,284,511 | G/C | — | uncertain significance |
| rs994323796 | X:153,284,663 | T/G | — | uncertain significance |
| rs2148643448 | X:153,284,689 | G/A | — | uncertain significance |
| rs2521947003 | X:153,284,694 | C/G | — | uncertain significance |
| rs201911518 | X:153,284,723 | T/G | — | benign |
| rs11465829 | X:153,284,746 | G/A | — | benign |
| rs200423500 | X:153,284,759 | G/A | — | uncertain significance |
| rs782636633 | X:153,285,057 | G/T | — | likely benign |
| rs2065769801 | X:153,285,238 | T/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.