ACOXL
acyl-CoA oxidase like
Summary
Predicted to enable acyl-CoA oxidase activity; fatty acid binding activity; and flavin adenine dinucleotide binding activity. Predicted to be involved in fatty acid beta-oxidation using acyl-CoA oxidase. Predicted to be located in peroxisomal matrix. Predicted to be active in peroxisome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs188422258 | 2:111,494,702 | T/A | intron variant | — |
| rs752696818 | 2:111,526,024 | C/T | — | uncertain significance |
| rs887505142 | 2:111,542,381 | A/G | — | uncertain significance |
| rs771820899 | 2:111,542,388 | T/A | — | uncertain significance |
| rs1684993535 | 2:111,551,684 | C/A | — | uncertain significance |
| rs369304472 | 2:111,551,686 | G/A | — | uncertain significance |
| rs201529913 | 2:111,551,731 | A/G | — | uncertain significance |
| rs551873770 | 2:111,556,218 | C/T | — | uncertain significance |
| rs748517725 | 2:111,556,283 | A/T | — | uncertain significance |
| rs933453806 | 2:111,556,597 | A/T | — | uncertain significance |
| rs764902890 | 2:111,556,600 | G/A | — | uncertain significance |
| rs1226948911 | 2:111,559,252 | A/G | — | uncertain significance |
| rs145955915 | 2:111,562,901 | T/C | — | uncertain significance |
| rs527716900 | 2:111,562,943 | G/T | — | uncertain significance |
| rs2467193378 | 2:111,562,965 | C/T | — | uncertain significance |
| rs12463442 | 2:111,595,489 | A/C | — | — |
| rs756146109 | 2:111,598,960 | A/G | — | uncertain significance |
| rs777944015 | 2:111,598,962 | A/G | — | uncertain significance |
| rs749321633 | 2:111,598,964 | C/G | — | uncertain significance |
| rs4849121 | 2:111,599,706 | G/T | — | — |
| rs10185010 | 2:111,601,798 | A/G | intron variant | — |
| rs7576541 | 2:111,607,401 | C/T | intron variant | — |
| rs6732565 | 2:111,607,832 | A/G | intron variant | — |
| rs10179923 | 2:111,609,690 | G/C | — | — |
| rs10180020 | 2:111,609,758 | G/T | — | — |
| rs62159471 | 2:111,615,421 | G/T | intron variant | — |
| rs13401811 | 2:111,616,104 | G/A | regulatory region variant | — |
| rs11898005 | 2:111,620,250 | G/A | intron variant | — |
| rs113122861 | 2:111,657,687 | C/A | — | — |
| rs6720034 | 2:111,664,756 | A/G | regulatory region variant | — |
| rs778800133 | 2:111,666,433 | C/T | — | likely benign |
| rs758543039 | 2:111,666,442 | C/A | — | uncertain significance |
| rs2469076684 | 2:111,691,071 | C/T | — | uncertain significance |
| rs373228229 | 2:111,691,122 | G/A | — | uncertain significance |
| rs1265915879 | 2:111,691,200 | G/A | — | uncertain significance |
| rs367553833 | 2:111,691,208 | A/G | — | uncertain significance |
| rs2060560004 | 2:111,691,211 | G/A | — | uncertain significance |
| rs10202539 | 2:111,702,545 | G/A | intron variant | — |
| rs3789119 | 2:111,707,405 | C/T | intron variant | — |
| rs4849303 | 2:111,728,482 | C/T | downstream gene variant | — |
| rs3789099 | 2:111,738,333 | C/T | intron variant | — |
| rs561949547 | 2:111,744,694 | C/T | — | uncertain significance |
| rs763217979 | 2:111,744,695 | G/A | — | likely benign |
| rs2062969247 | 2:111,744,725 | A/G | — | uncertain significance |
| rs1277970817 | 2:111,744,745 | G/C | — | uncertain significance |
| rs368763769 | 2:111,744,746 | G/A | — | uncertain significance |
| rs2062225 | 2:111,750,872 | A/C | — | — |
| rs148543890 | 2:111,753,553 | G/A | — | uncertain significance |
| rs11354102 | 2:111,776,288 | A/G | — | — |
| rs4849341 | 2:111,777,795 | C/A | — | — |
| rs11687123 | 2:111,784,320 | G/A | intron variant | — |
| rs59554295 | 2:111,785,143 | C/G | intron variant | — |
| rs56068469 | 2:111,786,637 | A/G | regulatory region variant | — |
| rs759297115 | 2:111,789,205 | T/C | — | uncertain significance |
| rs1158724274 | 2:111,789,255 | C/T | — | uncertain significance |
| rs2467065031 | 2:111,789,270 | T/G | — | uncertain significance |
| rs17483466 | 2:111,797,458 | A/G | intron variant | — |
| rs3789080 | 2:111,797,531 | C/T | intron variant | — |
| rs3827538 | 2:111,807,303 | T/G | — | — |
| rs9646934 | 2:111,822,002 | C/A | — | — |
| rs7578982 | 2:111,836,538 | T/C | intron variant | — |
| rs55711612 | 2:111,845,422 | A/T | — | — |
| rs10207392 | 2:111,849,659 | A/G | regulatory region variant | — |
| rs370944721 | 2:111,850,455 | A/G | — | uncertain significance |
| rs770996535 | 2:111,850,482 | G/T | — | uncertain significance |
| rs767616609 | 2:111,850,488 | G/T | — | uncertain significance |
| rs751027436 | 2:111,850,527 | C/T | — | likely benign |
| rs73954922 | 2:111,868,604 | A/C | intron variant | — |
| rs77004761 | 2:111,868,691 | T/A | intron variant | — |
| rs1439287 | 2:111,871,897 | G/A | upstream gene variant | — |
| rs72836344 | 2:111,874,699 | G/A | — | — |
| rs756959944 | 2:111,875,346 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.