ALOX15B
arachidonate 15-lipoxygenase type B
Summary
This gene encodes a member of the lipoxygenase family of structurally related nonheme iron dioxygenases involved in the production of fatty acid hydroperoxides. The encoded protein converts arachidonic acid exclusively to 15S-hydroperoxyeicosatetraenoic acid, while metabolizing linoleic acid less effectively. This gene is located in a cluster of related genes and a pseudogene that spans approximately 100 kilobases on the short arm of chromosome 17. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Known Variants58 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2545437005 | 17:7,942,570 | A/T | — | uncertain significance |
| rs577729599 | 17:7,942,582 | C/T | — | uncertain significance |
| rs771296412 | 17:7,942,592 | A/G | — | uncertain significance |
| rs776161988 | 17:7,942,768 | A/T | — | uncertain significance |
| rs765925684 | 17:7,942,794 | G/C | — | uncertain significance |
| rs200065292 | 17:7,942,807 | C/G | — | uncertain significance |
| rs368311556 | 17:7,942,824 | C/T | — | uncertain significance |
| rs772831605 | 17:7,942,848 | C/T | — | uncertain significance |
| rs767356851 | 17:7,942,868 | C/A | — | uncertain significance |
| rs917627708 | 17:7,942,869 | C/A | — | uncertain significance |
| rs577527240 | 17:7,943,249 | G/A | — | uncertain significance |
| rs763790373 | 17:7,943,275 | G/C | — | uncertain significance |
| rs139800287 | 17:7,945,725 | A/G | — | likely benign |
| rs1323112948 | 17:7,945,739 | G/A | — | likely benign |
| rs1277145991 | 17:7,945,743 | A/G | — | uncertain significance |
| rs905548726 | 17:7,946,148 | A/G | — | uncertain significance |
| rs750713821 | 17:7,946,179 | A/C | — | uncertain significance |
| rs143883230 | 17:7,948,152 | G/A | — | likely benign |
| rs141534086 | 17:7,948,239 | C/T | — | likely benign |
| rs567291621 | 17:7,948,253 | C/A | — | uncertain significance |
| rs201480696 | 17:7,948,257 | G/T | — | uncertain significance |
| rs367867264 | 17:7,948,269 | A/G | — | uncertain significance |
| rs146184262 | 17:7,948,293 | G/A | — | uncertain significance |
| rs1334742330 | 17:7,948,317 | G/C | — | uncertain significance |
| rs757377491 | 17:7,948,559 | G/A | — | uncertain significance |
| rs138883222 | 17:7,948,560 | G/A | — | uncertain significance |
| rs1246119436 | 17:7,948,602 | A/G | — | likely benign |
| rs367758401 | 17:7,948,680 | C/T | — | uncertain significance |
| rs149490685 | 17:7,948,693 | C/T | — | likely benign |
| rs111777159 | 17:7,948,795 | C/T | — | benign |
| rs145968454 | 17:7,948,829 | C/T | — | uncertain significance |
| rs2545444538 | 17:7,948,835 | T/G | — | uncertain significance |
| rs370434436 | 17:7,948,885 | C/T | — | uncertain significance |
| rs1250076835 | 17:7,948,897 | T/A | — | uncertain significance |
| rs2545444768 | 17:7,948,997 | T/C | — | uncertain significance |
| rs1196332160 | 17:7,950,071 | G/T | — | uncertain significance |
| rs1340334008 | 17:7,950,234 | A/G | — | uncertain significance |
| rs148578247 | 17:7,950,237 | G/A | — | uncertain significance |
| rs2545446289 | 17:7,950,289 | A/G | — | uncertain significance |
| rs1567972913 | 17:7,950,292 | C/G | — | uncertain significance |
| rs140623478 | 17:7,950,319 | G/A | — | uncertain significance |
| rs776991525 | 17:7,950,647 | C/A | — | uncertain significance |
| rs141549870 | 17:7,950,692 | G/A | — | uncertain significance |
| rs1179004665 | 17:7,950,933 | T/C | — | uncertain significance |
| rs1452165268 | 17:7,950,939 | T/C | — | uncertain significance |
| rs200616718 | 17:7,950,963 | C/T | — | uncertain significance |
| rs1976653211 | 17:7,951,080 | G/C | — | uncertain significance |
| rs144680641 | 17:7,951,153 | A/G | — | uncertain significance |
| rs372796583 | 17:7,951,720 | A/G | — | uncertain significance |
| rs768290223 | 17:7,951,723 | C/T | — | uncertain significance |
| rs771462763 | 17:7,951,752 | C/T | — | uncertain significance |
| rs61730298 | 17:7,951,756 | G/A | — | benign |
| rs761569403 | 17:7,951,772 | C/G | — | uncertain significance |
| rs368550756 | 17:7,951,804 | T/A | — | uncertain significance |
| rs369739171 | 17:7,951,813 | G/A | — | uncertain significance |
| rs535418281 | 17:7,951,851 | C/T | — | uncertain significance |
| rs201702180 | 17:7,951,872 | G/A | — | uncertain significance |
| rs7211013 | 17:7,952,759 | A/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.