IL32
interleukin 32
Summary
This gene encodes a member of the cytokine family. The protein contains a tyrosine sulfation site, 3 potential N-myristoylation sites, multiple putative phosphorylation sites, and an RGD cell-attachment sequence. Expression of this protein is increased after the activation of T-cells by mitogens or the activation of NK cells by IL-2. This protein induces the production of TNFalpha from macrophage cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs4786370 | 16:3,113,898 | T/C | downstream gene variant | — |
| rs28372698 | 16:3,115,111 | T/A | regulatory region variant | — |
| rs373456514 | 16:3,117,373 | C/T | — | likely benign |
| rs190241571 | 16:3,117,374 | G/A | — | benign |
| rs114354531 | 16:3,117,378 | G/A | — | benign |
| rs115923319 | 16:3,117,564 | A/C | — | benign |
| rs139541431 | 16:3,117,568 | A/G | — | uncertain significance |
| rs144473418 | 16:3,117,570 | A/G | — | benign |
| rs774782082 | 16:3,117,576 | T/C | — | uncertain significance |
| rs147775375 | 16:3,117,577 | A/G | — | benign |
| rs140063808 | 16:3,117,606 | C/T | — | uncertain significance |
| rs145687578 | 16:3,117,607 | G/A | — | likely benign |
| rs117009471 | 16:3,117,993 | G/A | — | benign |
| rs1385274355 | 16:3,117,998 | T/C | — | uncertain significance |
| rs766634927 | 16:3,118,005 | G/C | — | uncertain significance |
| rs369116355 | 16:3,118,171 | C/T | — | likely benign |
| rs1177739539 | 16:3,118,224 | A/C | — | uncertain significance |
| rs141583132 | 16:3,118,239 | C/T | — | benign |
| rs140322567 | 16:3,118,240 | A/G | — | benign |
| rs12934561 | 16:3,118,865 | T/A | — | — |
| rs2506957703 | 16:3,118,997 | A/G | — | uncertain significance |
| rs2506961565 | 16:3,119,087 | C/A | — | uncertain significance |
| rs764366058 | 16:3,119,091 | G/T | — | uncertain significance |
| rs1034287357 | 16:3,119,115 | T/G | — | uncertain significance |
| rs752000903 | 16:3,119,171 | G/C | — | uncertain significance |
| rs776480395 | 16:3,119,246 | T/C | — | uncertain significance |
| rs368991361 | 16:3,119,262 | T/C | — | uncertain significance |
| rs141220342 | 16:3,119,303 | G/A | — | uncertain significance |
| rs760045825 | 16:3,119,305 | C/G | — | uncertain significance |
| rs150738098 | 16:3,119,313 | A/G | — | uncertain significance |
| rs143941291 | 16:3,119,339 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.