ACAD11
acyl-CoA dehydrogenase family member 11
Summary
This gene encodes an acyl-CoA dehydrogenase enzyme with a preference for carbon chain lengths between 20 and 26. Naturally occurring read-through transcription occurs between the upstream gene NPHP3 (nephronophthisis 3 (adolescent)) and this gene. [provided by RefSeq, Aug 2015]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs781560688 | 3:132,277,847 | C/T | — | uncertain significance |
| rs140712582 | 3:132,277,849 | C/T | — | likely benign |
| rs780232149 | 3:132,277,856 | C/G | — | uncertain significance |
| rs778814949 | 3:132,277,865 | C/T | — | uncertain significance |
| rs757215751 | 3:132,277,906 | C/T | — | uncertain significance |
| rs2529901658 | 3:132,279,983 | T/C | — | uncertain significance |
| rs578141275 | 3:132,280,010 | G/A | — | uncertain significance |
| rs1456912128 | 3:132,280,014 | C/A | — | uncertain significance |
| rs1156397940 | 3:132,280,028 | T/C | — | uncertain significance |
| rs143271405 | 3:132,280,031 | G/A | — | uncertain significance |
| rs115823871 | 3:132,291,055 | C/T | intron variant | — |
| rs370980622 | 3:132,294,688 | C/T | — | likely benign |
| rs376159837 | 3:132,294,738 | G/A | — | uncertain significance |
| rs149300783 | 3:132,295,814 | C/T | — | uncertain significance |
| rs113194389 | 3:132,297,062 | G/T | regulatory region variant | — |
| rs142585652 | 3:132,297,725 | T/C | — | likely benign |
| rs2529962453 | 3:132,298,358 | T/C | — | uncertain significance |
| rs751359700 | 3:132,298,378 | A/G | — | uncertain significance |
| rs1937569350 | 3:132,298,388 | T/G | — | uncertain significance |
| rs113272668 | 3:132,302,982 | T/C | — | — |
| rs764000403 | 3:132,322,086 | T/A | — | uncertain significance |
| rs769960077 | 3:132,322,147 | G/A | — | uncertain significance |
| rs139371109 | 3:132,324,021 | C/T | — | uncertain significance |
| rs61292904 | 3:132,330,054 | A/G | intron variant | — |
| rs1397725961 | 3:132,331,305 | A/T | — | — |
| rs930841567 | 3:132,337,525 | G/C | — | uncertain significance |
| rs556232086 | 3:132,337,552 | A/C | — | uncertain significance |
| rs147696744 | 3:132,337,553 | C/T | — | uncertain significance |
| rs141257781 | 3:132,337,565 | C/T | — | uncertain significance |
| rs41272319 | 3:132,338,295 | G/A | downstream gene variant | — |
| rs2530105714 | 3:132,338,343 | C/A | — | uncertain significance |
| rs41272321 | 3:132,338,346 | T/C | missense variant | — |
| rs771424961 | 3:132,338,377 | A/G | — | uncertain significance |
| rs1033138466 | 3:132,345,536 | T/C | — | uncertain significance |
| rs768857711 | 3:132,345,593 | T/A | — | uncertain significance |
| rs2530132878 | 3:132,345,642 | G/A | — | uncertain significance |
| rs201521432 | 3:132,347,193 | A/T | — | uncertain significance |
| rs779885100 | 3:132,349,319 | G/A | — | uncertain significance |
| rs2530152432 | 3:132,350,206 | C/T | — | likely benign |
| rs140456617 | 3:132,360,866 | A/G | — | uncertain significance |
| rs143511938 | 3:132,361,564 | G/T | — | uncertain significance |
| rs140190064 | 3:132,361,606 | A/G | — | uncertain significance |
| rs756123908 | 3:132,363,714 | T/C | — | uncertain significance |
| rs1198353199 | 3:132,363,725 | A/C | — | uncertain significance |
| rs140950225 | 3:132,363,726 | T/C | — | uncertain significance |
| rs727503787 | 3:132,378,546 | T/G | — | uncertain significance |
| rs142799108 | 3:132,378,550 | G/A | — | uncertain significance |
| rs759636072 | 3:132,378,568 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.