ACSBG2
acyl-CoA synthetase bubblegum family member 2
Summary
Enables arachidonate-CoA ligase activity and fatty acyl-CoA hydrolase activity. Acts upstream of or within fatty acid metabolic process. Located in cytosol and mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2512591993 | 19:6,141,562 | G/A | — | likely benign |
| rs10401447 | 19:6,143,199 | T/C | — | — |
| rs2089074200 | 19:6,147,457 | T/G | — | uncertain significance |
| rs751364914 | 19:6,147,484 | G/A | — | uncertain significance |
| rs771329990 | 19:6,147,519 | G/A | — | uncertain significance |
| rs767294404 | 19:6,147,648 | T/C | — | uncertain significance |
| rs2145057119 | 19:6,151,775 | T/C | — | uncertain significance |
| rs758145719 | 19:6,156,479 | G/A | — | uncertain significance |
| rs754759877 | 19:6,161,240 | C/G | — | uncertain significance |
| rs535431440 | 19:6,161,257 | C/T | — | uncertain significance |
| rs768800626 | 19:6,161,288 | G/C | — | uncertain significance |
| rs768322863 | 19:6,165,909 | C/T | — | likely benign |
| rs200316550 | 19:6,165,937 | G/A | — | uncertain significance |
| rs781126332 | 19:6,177,244 | C/T | — | uncertain significance |
| rs141607717 | 19:6,177,261 | G/T | — | uncertain significance |
| rs764531996 | 19:6,177,305 | T/C | — | likely benign |
| rs765551838 | 19:6,177,326 | T/C | — | likely benign |
| rs750622613 | 19:6,177,328 | T/C | — | uncertain significance |
| rs535716280 | 19:6,181,069 | A/G | — | — |
| rs113123404 | 19:6,182,756 | A/C | — | benign |
| rs374130121 | 19:6,182,837 | C/T | — | uncertain significance |
| rs377656710 | 19:6,182,861 | G/C | — | uncertain significance |
| rs866017688 | 19:6,182,867 | T/A | — | uncertain significance |
| rs758197998 | 19:6,182,894 | G/A | — | uncertain significance |
| rs142334228 | 19:6,183,158 | G/A | — | benign |
| rs1331837953 | 19:6,183,210 | G/C | — | uncertain significance |
| rs374218452 | 19:6,185,461 | T/G | — | uncertain significance |
| rs764400524 | 19:6,185,557 | G/C | — | uncertain significance |
| rs765326702 | 19:6,185,569 | C/T | — | uncertain significance |
| rs1213147534 | 19:6,185,605 | C/G | — | uncertain significance |
| rs146836725 | 19:6,185,652 | G/A | — | uncertain significance |
| rs1274408332 | 19:6,187,294 | A/G | — | uncertain significance |
| rs2512271347 | 19:6,187,327 | C/T | — | uncertain significance |
| rs137960724 | 19:6,187,333 | T/C | — | uncertain significance |
| rs767667346 | 19:6,187,380 | G/A | — | uncertain significance |
| rs141620576 | 19:6,187,426 | C/T | — | uncertain significance |
| rs370382227 | 19:6,187,728 | A/T | — | uncertain significance |
| rs35609668 | 19:6,187,731 | C/G | — | benign |
| rs781417481 | 19:6,187,753 | G/T | — | uncertain significance |
| rs139700487 | 19:6,187,790 | A/G | — | uncertain significance |
| rs556102371 | 19:6,187,831 | C/A | — | uncertain significance |
| rs112210631 | 19:6,190,601 | T/C | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.