DAGLB
diacylglycerol lipase beta
Summary
Enables lipase activity. Involved in arachidonate metabolic process. Located in nucleoplasm and plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants80 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs702485 | 7:6,449,272 | A/G | 3 prime UTR variant | — |
| rs148435637 | 7:6,449,476 | C/T | — | uncertain significance |
| rs375537082 | 7:6,449,484 | C/T | — | likely benign |
| rs116243689 | 7:6,449,512 | C/T | — | benign |
| rs145993691 | 7:6,449,521 | C/T | — | benign |
| rs747539498 | 7:6,449,536 | C/T | — | uncertain significance |
| rs757156328 | 7:6,449,552 | C/T | — | uncertain significance |
| rs138127497 | 7:6,449,560 | T/C | — | likely benign |
| rs139129432 | 7:6,449,589 | G/A | — | uncertain significance |
| rs200184220 | 7:6,449,590 | G/C | — | uncertain significance |
| rs141846216 | 7:6,449,591 | A/G | — | likely benign |
| rs199735881 | 7:6,449,608 | T/A | — | uncertain significance |
| rs371012241 | 7:6,449,635 | C/T | — | uncertain significance |
| rs2534063870 | 7:6,449,658 | C/T | — | uncertain significance |
| rs139753251 | 7:6,449,794 | A/G | — | benign |
| rs143835290 | 7:6,449,879 | G/A | — | uncertain significance |
| rs146836483 | 7:6,449,903 | G/C | — | uncertain significance |
| rs755911500 | 7:6,449,911 | T/C | — | uncertain significance |
| rs779980426 | 7:6,449,914 | G/A | — | uncertain significance |
| rs80259222 | 7:6,449,947 | G/T | — | uncertain significance |
| rs1167474994 | 7:6,449,958 | G/T | — | uncertain significance |
| rs140957721 | 7:6,449,960 | T/C | — | likely benign |
| rs368066544 | 7:6,449,981 | C/T | — | uncertain significance |
| rs1023596095 | 7:6,449,993 | C/T | — | uncertain significance |
| rs775847806 | 7:6,449,994 | G/A | — | likely benign |
| rs73676731 | 7:6,450,020 | G/A | — | benign |
| rs149326625 | 7:6,452,470 | C/T | — | uncertain significance |
| rs751547204 | 7:6,452,476 | A/C | — | uncertain significance |
| rs766451252 | 7:6,452,492 | C/A | — | uncertain significance |
| rs537908568 | 7:6,452,622 | C/T | — | uncertain significance |
| rs4724803 | 7:6,453,808 | A/C | — | — |
| rs1562479268 | 7:6,456,270 | C/T | — | uncertain significance |
| rs1318401501 | 7:6,456,286 | C/T | — | uncertain significance |
| rs754358442 | 7:6,456,303 | G/A | — | uncertain significance |
| rs116541573 | 7:6,456,334 | G/A | — | benign |
| rs1055428 | 7:6,456,347 | G/C | synonymous variant | — |
| rs377177640 | 7:6,456,378 | C/T | — | uncertain significance |
| rs2534082660 | 7:6,456,474 | G/A | — | uncertain significance |
| rs2534082681 | 7:6,456,482 | C/T | — | uncertain significance |
| rs372411593 | 7:6,461,377 | T/A | — | uncertain significance |
| rs376696645 | 7:6,461,420 | G/T | — | uncertain significance |
| rs113080138 | 7:6,463,365 | C/G | intron variant | — |
| rs2534102894 | 7:6,464,450 | A/C | — | uncertain significance |
| rs149102582 | 7:6,465,705 | C/A | — | uncertain significance |
| rs766073926 | 7:6,465,722 | T/C | — | uncertain significance |
| rs112772921 | 7:6,470,206 | G/A | — | likely benign |
| rs754065964 | 7:6,470,210 | T/C | — | uncertain significance |
| rs200811468 | 7:6,470,218 | T/A | — | uncertain significance |
| rs200368991 | 7:6,472,528 | G/T | — | uncertain significance |
| rs766954204 | 7:6,472,541 | T/C | — | uncertain significance |
| rs751467052 | 7:6,472,552 | G/A | — | likely benign |
| rs61732628 | 7:6,472,558 | C/T | — | benign |
| rs768031457 | 7:6,472,587 | T/C | — | uncertain significance |
| rs1363764030 | 7:6,474,412 | A/C | — | uncertain significance |
| rs747533000 | 7:6,474,433 | G/A | — | uncertain significance |
| rs140011587 | 7:6,474,437 | C/G | — | uncertain significance |
| rs368951817 | 7:6,474,471 | C/G | — | uncertain significance |
| rs758563828 | 7:6,474,497 | C/T | — | uncertain significance |
| rs2534125314 | 7:6,474,511 | G/T | — | uncertain significance |
| rs2534125362 | 7:6,474,539 | A/G | — | uncertain significance |
| rs764347543 | 7:6,474,566 | C/G | — | uncertain significance |
| rs747733355 | 7:6,474,602 | G/C | — | uncertain significance |
| rs2534125615 | 7:6,474,634 | G/C | — | uncertain significance |
| rs2534125620 | 7:6,474,637 | G/A | — | uncertain significance |
| rs764153612 | 7:6,474,638 | C/T | — | uncertain significance |
| rs145348882 | 7:6,476,019 | G/A | — | likely benign |
| rs1236086194 | 7:6,476,021 | T/A | — | uncertain significance |
| rs374065896 | 7:6,476,024 | C/G | — | uncertain significance |
| rs780996250 | 7:6,476,026 | A/C | — | uncertain significance |
| rs1158914413 | 7:6,476,036 | C/T | — | uncertain significance |
| rs886249851 | 7:6,476,123 | G/C | — | uncertain significance |
| rs836545 | 7:6,479,410 | C/T | intron variant | — |
| rs836546 | 7:6,479,668 | G/A | intron variant | — |
| rs374025101 | 7:6,485,604 | A/T | — | uncertain significance |
| rs756285755 | 7:6,485,644 | T/C | — | uncertain significance |
| rs2534152187 | 7:6,485,712 | T/C | — | uncertain significance |
| rs7797644 | 7:6,486,067 | T/A | — | — |
| rs775518563 | 7:6,487,440 | C/T | — | uncertain significance |
| rs1458578076 | 7:6,487,458 | G/C | — | uncertain significance |
| rs7807755 | 7:6,488,097 | T/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.