ACOT11
acyl-CoA thioesterase 11
Summary
This gene encodes a member of the acyl-CoA thioesterase family which catalyse the conversion of activated fatty acids to the corresponding non-esterified fatty acid and coenzyme A. Expression of a mouse homolog in brown adipose tissue is induced by low temperatures and repressed by warm temperatures. Higher levels of expression of the mouse homolog has been found in obesity-resistant mice compared with obesity-prone mice, suggesting a role of acyl-CoA thioesterase 11 in obesity. Alternative splicing results in transcript variants. [provided by RefSeq, Nov 2010]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs201305708 | 1:55,050,361 | C/T | — | uncertain significance |
| rs150203501 | 1:55,050,380 | C/T | — | uncertain significance |
| rs139052769 | 1:55,050,418 | C/T | — | uncertain significance |
| rs114153052 | 1:55,050,453 | G/A | — | benign |
| rs1332546596 | 1:55,050,455 | T/C | — | uncertain significance |
| rs1445550223 | 1:55,051,550 | A/G | — | uncertain significance |
| rs2524913849 | 1:55,058,230 | T/G | — | uncertain significance |
| rs201270006 | 1:55,060,248 | C/T | — | uncertain significance |
| rs1397882472 | 1:55,060,254 | G/A | — | uncertain significance |
| rs773143384 | 1:55,060,298 | C/T | — | uncertain significance |
| rs551000440 | 1:55,060,299 | G/A | — | uncertain significance |
| rs1176342736 | 1:55,060,302 | G/A | — | uncertain significance |
| rs1654831638 | 1:55,060,313 | G/A | — | uncertain significance |
| rs149264358 | 1:55,060,317 | A/G | — | uncertain significance |
| rs754546540 | 1:55,060,348 | C/G | — | uncertain significance |
| rs149789097 | 1:55,062,949 | T/C | — | uncertain significance |
| rs373866115 | 1:55,062,955 | C/T | — | uncertain significance |
| rs146513780 | 1:55,062,965 | C/T | — | uncertain significance |
| rs2524931755 | 1:55,062,968 | C/A | — | uncertain significance |
| rs751016639 | 1:55,063,004 | T/C | — | uncertain significance |
| rs768931947 | 1:55,063,042 | G/A | — | uncertain significance |
| rs141264387 | 1:55,064,971 | G/A | — | uncertain significance |
| rs140890441 | 1:55,065,094 | G/T | — | benign |
| rs144192149 | 1:55,066,967 | G/A | — | uncertain significance |
| rs781051947 | 1:55,066,973 | C/T | — | uncertain significance |
| rs745370762 | 1:55,066,974 | G/A | — | uncertain significance |
| rs201446509 | 1:55,067,073 | G/C | — | uncertain significance |
| rs138616777 | 1:55,068,351 | C/T | — | uncertain significance |
| rs778640519 | 1:55,068,355 | G/A | — | uncertain significance |
| rs765942343 | 1:55,068,388 | G/T | — | uncertain significance |
| rs749372318 | 1:55,069,603 | G/C | — | uncertain significance |
| rs768894868 | 1:55,069,608 | C/G | — | uncertain significance |
| rs12038884 | 1:55,070,030 | C/G | — | uncertain significance |
| rs200872982 | 1:55,070,053 | A/C | — | uncertain significance |
| rs34148246 | 1:55,070,089 | C/T | — | likely benign |
| rs1569767221 | 1:55,072,816 | G/T | — | uncertain significance |
| rs540502406 | 1:55,072,900 | C/G | — | uncertain significance |
| rs771940818 | 1:55,072,901 | G/A | — | uncertain significance |
| rs770420515 | 1:55,072,913 | T/A | — | uncertain significance |
| rs78753605 | 1:55,073,630 | C/T | — | benign |
| rs377418362 | 1:55,073,632 | C/T | — | uncertain significance |
| rs752235009 | 1:55,073,635 | T/C | — | uncertain significance |
| rs758288650 | 1:55,073,640 | T/C | — | uncertain significance |
| rs138502889 | 1:55,073,668 | C/T | — | uncertain significance |
| rs756350557 | 1:55,073,683 | G/A | — | uncertain significance |
| rs375908312 | 1:55,073,697 | T/C | — | uncertain significance |
| rs115702810 | 1:55,073,750 | G/A | — | benign |
| rs2289015 | 1:55,075,062 | C/A | missense variant | — |
| rs733035 | 1:55,076,430 | G/A | — | benign |
| rs11206397 | 1:55,097,068 | A/C | — | — |
| rs11206398 | 1:55,097,106 | A/T | — | — |
| rs4927145 | 1:55,098,750 | A/G | upstream gene variant | — |
| rs140275361 | 1:55,100,021 | T/C | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.