GFPT2
glutamine--fructose-6-phosphate transaminase 2
Summary
Enables glutamine-fructose-6-phosphate transaminase (isomerizing) activity. Involved in UDP-N-acetylglucosamine biosynthetic process and fructose 6-phosphate metabolic process. Predicted to be located in cytosol. Implicated in type 2 diabetes mellitus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants55 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11748619 | 5:179,727,399 | C/A | — | — |
| rs7725 | 5:179,727,957 | C/G | — | — |
| rs372543131 | 5:179,728,546 | C/T | — | likely benign |
| rs185799471 | 5:179,729,440 | C/G | — | uncertain significance |
| rs376145345 | 5:179,729,476 | C/T | — | uncertain significance |
| rs371527867 | 5:179,729,555 | G/A | — | likely benign |
| rs2080955 | 5:179,730,004 | T/C | intron variant | — |
| rs6879260 | 5:179,731,014 | T/G | — | — |
| rs751065674 | 5:179,731,777 | G/A | — | uncertain significance |
| rs755738463 | 5:179,731,876 | G/T | — | uncertain significance |
| rs376225831 | 5:179,731,879 | C/T | — | uncertain significance |
| rs375131566 | 5:179,731,901 | G/C | — | uncertain significance |
| rs1763746851 | 5:179,731,928 | C/G | — | uncertain significance |
| rs7706951 | 5:179,733,407 | C/T | intron variant | — |
| rs10903252 | 5:179,733,934 | T/C | intron variant | — |
| rs11741142 | 5:179,734,139 | T/A | intron variant | — |
| rs761411762 | 5:179,734,241 | T/G | — | uncertain significance |
| rs36046599 | 5:179,739,451 | G/A | — | uncertain significance |
| rs113096165 | 5:179,740,366 | C/G | — | — |
| rs1443773342 | 5:179,740,818 | C/T | — | uncertain significance |
| rs371138776 | 5:179,740,869 | G/A | — | uncertain significance |
| rs1581372179 | 5:179,740,880 | C/T | — | uncertain significance |
| rs1012796939 | 5:179,740,899 | C/T | — | uncertain significance |
| rs201795453 | 5:179,740,949 | G/A | — | uncertain significance |
| rs190432524 | 5:179,742,263 | C/T | intron variant | — |
| rs2480736260 | 5:179,743,354 | G/C | — | uncertain significance |
| rs368601222 | 5:179,743,365 | C/T | — | uncertain significance |
| rs2480736367 | 5:179,743,383 | G/A | — | uncertain significance |
| rs1764011788 | 5:179,743,457 | C/T | — | uncertain significance |
| rs770615577 | 5:179,743,763 | C/T | — | uncertain significance |
| rs202097862 | 5:179,743,810 | C/T | — | uncertain significance |
| rs35765078 | 5:179,745,854 | G/A | — | benign |
| rs1299885738 | 5:179,745,949 | T/C | — | uncertain significance |
| rs6896556 | 5:179,747,511 | A/C | — | — |
| rs561071820 | 5:179,751,216 | C/T | — | uncertain significance |
| rs191781621 | 5:179,751,217 | G/A | — | likely benign |
| rs773009551 | 5:179,751,219 | C/A | — | uncertain significance |
| rs201867122 | 5:179,751,246 | C/T | — | likely benign |
| rs780260577 | 5:179,751,273 | T/C | — | uncertain significance |
| rs1764171794 | 5:179,751,278 | C/G | — | uncertain significance |
| rs1359672065 | 5:179,751,854 | T/C | — | uncertain significance |
| rs751339440 | 5:179,755,278 | G/A | — | uncertain significance |
| rs1432277572 | 5:179,757,759 | T/G | — | uncertain significance |
| rs747300251 | 5:179,757,774 | T/G | — | uncertain significance |
| rs763256022 | 5:179,757,824 | C/G | — | uncertain significance |
| rs4700942 | 5:179,761,163 | G/C | regulatory region variant | — |
| rs760185269 | 5:179,762,846 | G/A | — | uncertain significance |
| rs1004591553 | 5:179,762,876 | C/A | — | uncertain significance |
| rs558612701 | 5:179,762,941 | A/G | — | uncertain significance |
| rs199538381 | 5:179,763,552 | G/A | — | likely benign |
| rs372601171 | 5:179,763,560 | T/G | — | uncertain significance |
| rs115140594 | 5:179,765,506 | G/A | — | likely benign |
| rs369442859 | 5:179,765,522 | C/T | — | uncertain significance |
| rs750858375 | 5:179,765,547 | C/T | — | uncertain significance |
| rs9686363 | 5:179,767,597 | C/T | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.