FUT5
fucosyltransferase 5
Summary
Enables 3-galactosyl-N-acetylglucosaminide 4-alpha-L-fucosyltransferase activity and 4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase activity. Involved in ceramide metabolic process; oligosaccharide metabolic process; and protein glycosylation. Predicted to be located in Golgi membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs754359097 | 19:5,866,631 | A/T | — | uncertain significance |
| rs145948674 | 19:5,866,638 | G/A | — | uncertain significance |
| rs747064405 | 19:5,866,640 | A/G | — | uncertain significance |
| rs368467966 | 19:5,866,643 | G/A | — | uncertain significance |
| rs760438160 | 19:5,866,662 | G/C | — | likely benign |
| rs1258625481 | 19:5,866,679 | G/T | — | uncertain significance |
| rs4807054 | 19:5,866,724 | G/A | — | benign |
| rs201483736 | 19:5,866,730 | C/T | — | uncertain significance |
| rs778984 | 19:5,866,736 | T/C | — | benign |
| rs779925260 | 19:5,866,761 | G/A | — | uncertain significance |
| rs769145980 | 19:5,866,791 | C/T | — | uncertain significance |
| rs141679775 | 19:5,866,836 | C/T | — | uncertain significance |
| rs781164561 | 19:5,866,854 | C/G | — | uncertain significance |
| rs760071180 | 19:5,866,884 | C/T | — | uncertain significance |
| rs780790781 | 19:5,866,907 | G/A | — | uncertain significance |
| rs201842894 | 19:5,866,938 | C/T | — | uncertain significance |
| rs147659571 | 19:5,866,967 | T/C | — | uncertain significance |
| rs372756609 | 19:5,866,969 | G/C | — | uncertain significance |
| rs759478889 | 19:5,866,980 | G/A | — | uncertain significance |
| rs143372058 | 19:5,866,988 | G/A | — | uncertain significance |
| rs61730514 | 19:5,867,007 | T/G | — | likely benign |
| rs371757001 | 19:5,867,040 | C/T | — | uncertain significance |
| rs145832499 | 19:5,867,054 | G/A | — | uncertain significance |
| rs189013086 | 19:5,867,086 | C/T | — | likely benign |
| rs1460152223 | 19:5,867,087 | G/A | — | uncertain significance |
| rs774312190 | 19:5,867,093 | G/A | — | uncertain significance |
| rs374990298 | 19:5,867,111 | G/A | — | likely benign |
| rs142429483 | 19:5,867,127 | C/T | — | likely benign |
| rs756509874 | 19:5,867,144 | T/C | — | uncertain significance |
| rs771067259 | 19:5,867,150 | G/A | — | uncertain significance |
| rs769726197 | 19:5,867,198 | G/A | — | uncertain significance |
| rs61731581 | 19:5,867,208 | C/T | — | uncertain significance |
| rs767078141 | 19:5,867,217 | T/G | — | likely benign |
| rs1448700231 | 19:5,867,263 | G/T | — | likely benign |
| rs371889398 | 19:5,867,267 | C/T | — | uncertain significance |
| rs771920745 | 19:5,867,268 | G/A | — | uncertain significance |
| rs760315315 | 19:5,867,289 | T/A | — | uncertain significance |
| rs764635014 | 19:5,867,291 | C/T | — | uncertain significance |
| rs201253650 | 19:5,867,393 | T/C | — | uncertain significance |
| rs536359180 | 19:5,867,430 | C/T | — | uncertain significance |
| rs566802540 | 19:5,867,453 | G/A | — | uncertain significance |
| rs189234701 | 19:5,867,469 | C/A | — | uncertain significance |
| rs141356302 | 19:5,867,472 | C/T | — | likely benign |
| rs754840078 | 19:5,867,513 | G/T | — | uncertain significance |
| rs371381431 | 19:5,867,558 | T/C | — | uncertain significance |
| rs2057509723 | 19:5,867,559 | T/C | — | uncertain significance |
| rs767284783 | 19:5,867,577 | G/T | — | uncertain significance |
| rs763909943 | 19:5,867,634 | G/A | — | uncertain significance |
| rs528295486 | 19:5,867,655 | C/T | — | uncertain significance |
| rs755351741 | 19:5,867,682 | C/T | — | uncertain significance |
| rs561364366 | 19:5,867,694 | G/A | — | uncertain significance |
| rs777895417 | 19:5,867,696 | C/T | — | uncertain significance |
| rs764851768 | 19:5,867,730 | G/T | — | uncertain significance |
| rs564112601 | 19:5,869,879 | G/A | — | — |
| rs113243450 | 19:5,871,367 | G/A | regulatory region variant | — |
| rs12982903 | 19:5,872,403 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.