TREH
trehalase
Summary
This gene encodes an enzyme that hydrolyses trehalose, a disaccharide formed from two glucose molecules found mainly in fungi, plants, and insects. A partial duplication of this gene is located adjacent to this locus on chromosome 11. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2014]
Known Variants74 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs7389 | 11:118,528,466 | T/G | downstream gene variant | — |
| rs200772007 | 11:118,529,054 | G/A | — | uncertain significance |
| rs782706367 | 11:118,529,057 | G/T | — | uncertain significance |
| rs569450562 | 11:118,529,092 | C/T | — | uncertain significance |
| rs2500838086 | 11:118,529,125 | A/T | — | uncertain significance |
| rs7928371 | 11:118,529,127 | G/A | — | benign |
| rs573517484 | 11:118,529,147 | C/T | — | uncertain significance |
| rs557922859 | 11:118,529,263 | A/C | — | — |
| rs782616666 | 11:118,529,394 | C/T | — | uncertain significance |
| rs2500841089 | 11:118,529,398 | A/G | — | likely benign |
| rs2500841094 | 11:118,529,400 | A/G | — | uncertain significance |
| rs191186222 | 11:118,529,414 | C/T | — | uncertain significance |
| rs782362029 | 11:118,529,433 | T/C | — | uncertain significance |
| rs556006762 | 11:118,529,624 | A/G | — | likely benign |
| rs201467126 | 11:118,529,634 | T/A | — | uncertain significance |
| rs200074060 | 11:118,529,635 | C/A | — | uncertain significance |
| rs781886545 | 11:118,529,664 | T/C | — | uncertain significance |
| rs202164923 | 11:118,529,702 | C/T | — | uncertain significance |
| rs2276064 | 11:118,529,703 | G/A | missense variant | — |
| rs1555144331 | 11:118,530,136 | C/T | — | uncertain significance |
| rs782653438 | 11:118,530,156 | G/A | — | uncertain significance |
| rs11827611 | 11:118,530,166 | A/G | — | likely benign |
| rs117619140 | 11:118,530,434 | G/A | — | — |
| rs2500846912 | 11:118,530,470 | G/C | — | uncertain significance |
| rs782261584 | 11:118,530,485 | C/T | — | uncertain significance |
| rs1490428895 | 11:118,530,544 | C/T | — | likely benign |
| rs2276065 | 11:118,530,611 | C/T | — | benign |
| rs782068563 | 11:118,530,621 | G/A | — | likely benign |
| rs1555144557 | 11:118,530,667 | T/C | — | uncertain significance |
| rs371512027 | 11:118,531,249 | C/T | — | likely benign |
| rs782054608 | 11:118,531,265 | T/C | — | uncertain significance |
| rs781906034 | 11:118,531,284 | C/T | — | uncertain significance |
| rs782747796 | 11:118,531,288 | G/A | — | likely benign |
| rs140687140 | 11:118,531,335 | T/C | — | benign |
| rs200440695 | 11:118,531,367 | A/G | — | likely benign |
| rs373972077 | 11:118,531,398 | A/C | — | uncertain significance |
| rs201279957 | 11:118,531,437 | G/A | — | uncertain significance |
| rs782679595 | 11:118,531,872 | G/T | — | uncertain significance |
| rs1392933253 | 11:118,531,900 | T/G | — | uncertain significance |
| rs202074487 | 11:118,531,918 | C/T | — | uncertain significance |
| rs2500851020 | 11:118,531,954 | A/G | — | uncertain significance |
| rs782533738 | 11:118,531,958 | G/A | — | likely benign |
| rs200534594 | 11:118,532,112 | C/T | — | likely benign |
| rs372238200 | 11:118,532,113 | G/C | — | likely benign |
| rs782245431 | 11:118,532,162 | G/A | — | uncertain significance |
| rs781966736 | 11:118,532,191 | G/A | — | likely benign |
| rs535722007 | 11:118,532,193 | G/A | — | uncertain significance |
| rs782713762 | 11:118,532,387 | C/T | — | likely benign |
| rs368350996 | 11:118,532,624 | C/T | — | uncertain significance |
| rs1949328591 | 11:118,532,660 | G/T | — | uncertain significance |
| rs377353940 | 11:118,532,668 | C/T | — | likely benign |
| rs181334055 | 11:118,532,708 | G/A | — | likely benign |
| rs2500855341 | 11:118,533,584 | T/A | — | likely benign |
| rs34978247 | 11:118,533,594 | T/C | — | likely benign |
| rs561710627 | 11:118,533,625 | G/T | — | uncertain significance |
| rs2500855564 | 11:118,533,657 | A/C | — | uncertain significance |
| rs983517515 | 11:118,533,803 | C/T | — | uncertain significance |
| rs535480211 | 11:118,533,837 | G/T | — | uncertain significance |
| rs781987530 | 11:118,533,847 | C/T | — | likely benign |
| rs782821030 | 11:118,533,884 | G/A | — | uncertain significance |
| rs115405278 | 11:118,533,904 | T/C | — | likely benign |
| rs2137267752 | 11:118,534,062 | A/C | — | uncertain significance |
| rs10790256 | 11:118,534,082 | C/T | synonymous variant | benign |
| rs200713103 | 11:118,534,113 | A/G | — | uncertain significance |
| rs367691202 | 11:118,534,117 | G/T | — | uncertain significance |
| rs868937423 | 11:118,534,127 | C/T | — | likely benign |
| rs544711669 | 11:118,534,279 | C/T | — | — |
| rs12225548 | 11:118,535,840 | C/G | intron variant | — |
| rs534376033 | 11:118,536,946 | A/T | — | — |
| rs506234 | 11:118,540,104 | C/A | — | — |
| rs571912224 | 11:118,542,314 | G/A | — | — |
| rs187062573 | 11:118,548,412 | C/T | intron variant | — |
| rs507080 | 11:118,549,582 | G/A | regulatory region variant | — |
| rs186759385 | 11:118,551,561 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.