DAGLA
diacylglycerol lipase alpha
Summary
This gene encodes a diacylglycerol lipase. The encoded enzyme is involved in the biosynthesis of the endocannabinoid 2-arachidonoyl-glycerol.[provided by RefSeq, Nov 2010]
Known Variants89 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138417087 | 11:61,448,996 | G/A | intron variant | — |
| rs534116551 | 11:61,450,323 | C/G | — | — |
| rs139464416 | 11:61,452,342 | A/G | intron variant | — |
| rs11827215 | 11:61,458,595 | G/A | intron variant | — |
| rs144221952 | 11:61,460,127 | G/A | intron variant | — |
| rs533665305 | 11:61,463,351 | C/T | — | — |
| rs149362147 | 11:61,470,630 | G/A | intron variant | — |
| rs79250201 | 11:61,475,195 | G/A | regulatory region variant | — |
| rs146338176 | 11:61,480,075 | A/G | intron variant | — |
| rs2017861 | 11:61,481,928 | G/A | intron variant | — |
| rs555405975 | 11:61,487,510 | T/G | — | — |
| rs142265242 | 11:61,487,639 | C/T | — | likely benign |
| rs198430 | 11:61,487,690 | G/A | — | benign |
| rs776542702 | 11:61,488,179 | G/A | — | uncertain significance |
| rs2540723390 | 11:61,488,216 | A/G | — | uncertain significance |
| rs753243808 | 11:61,488,221 | G/A | — | uncertain significance |
| rs201994401 | 11:61,488,301 | C/T | — | likely benign |
| rs192081213 | 11:61,489,874 | A/G | intron variant | — |
| rs2065296298 | 11:61,490,403 | A/G | — | uncertain significance |
| rs198426 | 11:61,490,486 | C/T | intron variant | — |
| rs199919138 | 11:61,490,902 | G/A | — | likely benign |
| rs114103951 | 11:61,490,967 | C/T | — | benign |
| rs117022401 | 11:61,492,620 | C/G | intron variant | — |
| rs4963243 | 11:61,494,327 | G/A | intron variant | — |
| rs748974217 | 11:61,495,731 | G/A | — | uncertain significance |
| rs1208820167 | 11:61,495,745 | G/A | — | uncertain significance |
| rs771001941 | 11:61,495,757 | G/A | — | uncertain significance |
| rs113263760 | 11:61,495,943 | C/T | regulatory region variant | — |
| rs372368804 | 11:61,496,411 | T/C | — | likely benign |
| rs198416 | 11:61,496,682 | A/G | regulatory region variant | — |
| rs2540738205 | 11:61,498,795 | A/T | — | uncertain significance |
| rs2540738236 | 11:61,498,820 | A/G | — | uncertain significance |
| rs2100026321 | 11:61,498,874 | A/G | — | uncertain significance |
| rs148950289 | 11:61,500,020 | C/T | intron variant | — |
| rs73485460 | 11:61,502,351 | C/T | — | benign |
| rs768257190 | 11:61,502,367 | A/G | — | uncertain significance |
| rs139298962 | 11:61,502,410 | G/A | — | uncertain significance |
| rs761453740 | 11:61,502,474 | G/A | — | likely benign |
| rs749287274 | 11:61,503,071 | C/A | — | uncertain significance |
| rs2540746198 | 11:61,504,661 | G/T | — | uncertain significance |
| rs198444 | 11:61,505,168 | G/A | — | benign |
| rs774235898 | 11:61,505,186 | G/A | — | likely benign |
| rs199778275 | 11:61,506,933 | G/A | — | likely benign |
| rs143436889 | 11:61,507,013 | C/G | — | likely benign |
| rs145797037 | 11:61,507,065 | C/G | — | likely benign |
| rs1430051049 | 11:61,507,070 | C/T | — | uncertain significance |
| rs57220536 | 11:61,507,473 | C/A | intron variant | — |
| rs4963255 | 11:61,507,606 | G/A | intron variant | — |
| rs11828739 | 11:61,508,074 | C/T | — | benign |
| rs139319330 | 11:61,508,127 | G/A | intron variant | — |
| rs2065475750 | 11:61,508,657 | G/C | — | likely benign |
| rs373949198 | 11:61,508,702 | C/A | — | likely benign |
| rs1358091747 | 11:61,508,797 | C/T | — | uncertain significance |
| rs368442690 | 11:61,508,817 | G/A | — | uncertain significance |
| rs2065501315 | 11:61,511,024 | T/C | — | uncertain significance |
| rs35056845 | 11:61,511,036 | G/T | — | benign |
| rs765951660 | 11:61,511,076 | G/A | — | likely benign |
| rs149360213 | 11:61,511,078 | C/T | — | likely benign |
| rs144674730 | 11:61,511,081 | C/T | — | likely benign |
| rs565066817 | 11:61,511,093 | C/T | — | uncertain significance |
| rs2540756148 | 11:61,511,114 | C/T | — | uncertain significance |
| rs3741251 | 11:61,511,133 | G/A | — | benign |
| rs541505185 | 11:61,511,149 | C/T | — | uncertain significance |
| rs140475905 | 11:61,511,150 | G/A | — | uncertain significance |
| rs2540756298 | 11:61,511,202 | C/G | — | pathogenic |
| rs34365114 | 11:61,511,271 | G/A | — | benign |
| rs2540756474 | 11:61,511,272 | G/T | — | pathogenic |
| rs563501324 | 11:61,511,300 | T/C | — | uncertain significance |
| rs373810848 | 11:61,511,316 | C/T | — | likely benign |
| rs998640015 | 11:61,511,317 | G/T | — | pathogenic |
| rs2540756654 | 11:61,511,345 | C/T | — | uncertain significance |
| rs2065508523 | 11:61,511,383 | C/T | — | likely pathogenic |
| rs200294323 | 11:61,511,405 | C/T | missense variant | — |
| rs746432570 | 11:61,511,437 | C/T | — | uncertain significance |
| rs373392668 | 11:61,511,463 | C/A | — | likely benign |
| rs552427376 | 11:61,511,493 | C/T | — | likely benign |
| rs3741252 | 11:61,511,498 | C/T | — | benign |
| rs771641156 | 11:61,511,506 | C/T | — | uncertain significance |
| rs775544867 | 11:61,511,636 | G/A | — | uncertain significance |
| rs763023855 | 11:61,511,641 | G/T | — | uncertain significance |
| rs1591057945 | 11:61,511,687 | C/T | — | uncertain significance |
| rs1391121972 | 11:61,511,725 | G/A | — | uncertain significance |
| rs117050893 | 11:61,511,794 | C/G | — | benign |
| rs774144925 | 11:61,511,843 | C/T | — | uncertain significance |
| rs765568409 | 11:61,511,849 | C/T | — | uncertain significance |
| rs1294742345 | 11:61,511,868 | A/T | — | uncertain significance |
| rs199764983 | 11:61,511,881 | G/C | — | uncertain significance |
| rs1243312076 | 11:61,511,902 | C/G | — | uncertain significance |
| rs775061931 | 11:61,511,957 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.