ACSM5
acyl-CoA synthetase medium chain family member 5
Summary
Predicted to enable fatty acid ligase activity and fatty-acyl-CoA synthase activity. Predicted to be involved in acyl-CoA metabolic process and fatty acid biosynthetic process. Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs370540779 | 16:20,422,971 | C/T | — | likely benign |
| rs1424983914 | 16:20,429,438 | A/G | — | likely benign |
| rs138928573 | 16:20,429,486 | A/C | — | uncertain significance |
| rs146077452 | 16:20,429,580 | G/T | — | uncertain significance |
| rs771212949 | 16:20,430,717 | A/T | — | uncertain significance |
| rs373907643 | 16:20,430,723 | C/T | — | uncertain significance |
| rs533410184 | 16:20,430,756 | C/T | — | uncertain significance |
| rs747352575 | 16:20,432,594 | A/C | — | uncertain significance |
| rs753814935 | 16:20,432,698 | G/A | — | uncertain significance |
| rs2548850776 | 16:20,432,716 | A/G | — | uncertain significance |
| rs542345418 | 16:20,432,719 | G/A | — | uncertain significance |
| rs566907774 | 16:20,435,239 | C/T | — | uncertain significance |
| rs773126951 | 16:20,435,315 | T/C | — | uncertain significance |
| rs771981131 | 16:20,435,327 | G/T | — | uncertain significance |
| rs747860842 | 16:20,435,381 | T/C | — | uncertain significance |
| rs138922279 | 16:20,439,111 | C/T | — | uncertain significance |
| rs200496913 | 16:20,439,128 | A/G | — | uncertain significance |
| rs2548853296 | 16:20,439,182 | C/G | — | uncertain significance |
| rs11859961 | 16:20,439,199 | G/A | — | benign |
| rs2548854047 | 16:20,441,031 | A/C | — | uncertain significance |
| rs762707021 | 16:20,441,057 | C/T | — | likely benign |
| rs1448861681 | 16:20,441,072 | G/T | — | uncertain significance |
| rs12931877 | 16:20,441,077 | A/G | — | benign |
| rs2548854138 | 16:20,441,121 | A/G | — | uncertain significance |
| rs148243446 | 16:20,442,346 | A/C | — | not provided |
| rs2548854875 | 16:20,442,549 | A/G | — | uncertain significance |
| rs764517848 | 16:20,442,558 | G/A | — | uncertain significance |
| rs138834094 | 16:20,442,594 | C/T | — | likely benign |
| rs768981168 | 16:20,442,609 | C/G | — | uncertain significance |
| rs12924989 | 16:20,442,926 | T/C | intron variant | — |
| rs66465511 | 16:20,447,332 | T/A | — | — |
| rs201184714 | 16:20,448,401 | G/A | — | uncertain significance |
| rs141553052 | 16:20,448,438 | G/T | — | uncertain significance |
| rs147520476 | 16:20,448,451 | T/A | — | uncertain significance |
| rs566445704 | 16:20,448,474 | G/A | — | uncertain significance |
| rs769546454 | 16:20,448,486 | T/A | — | uncertain significance |
| rs774501153 | 16:20,448,679 | T/C | — | uncertain significance |
| rs768006269 | 16:20,448,685 | G/T | — | uncertain significance |
| rs11647589 | 16:20,449,616 | A/G | regulatory region variant | — |
| rs778890369 | 16:20,451,143 | C/G | — | uncertain significance |
| rs554734865 | 16:20,451,183 | C/T | — | uncertain significance |
| rs777898691 | 16:20,451,204 | T/A | — | uncertain significance |
| rs2548858161 | 16:20,451,224 | T/C | — | uncertain significance |
| rs762291076 | 16:20,451,233 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.