GLCE
glucuronic acid epimerase
Summary
Enables calcium ion binding activity; heparosan-N-sulfate-glucuronate 5-epimerase activity; and protein homodimerization activity. Involved in heparan sulfate proteoglycan biosynthetic process. Predicted to be located in Golgi membrane. Predicted to be active in Golgi apparatus. Implicated in cerebrovascular disease and hypertension. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11629932 | 15:69,535,958 | T/C | upstream gene variant | — |
| rs35810867 | 15:69,536,159 | A/T | upstream gene variant | — |
| rs138637994 | 15:69,548,197 | G/A | — | uncertain significance |
| rs1809477471 | 15:69,548,249 | A/G | — | uncertain significance |
| rs1702784096 | 15:69,548,259 | G/T | — | uncertain significance |
| rs201399708 | 15:69,548,266 | C/T | — | uncertain significance |
| rs745504393 | 15:69,548,303 | A/C | — | uncertain significance |
| rs184777253 | 15:69,548,347 | G/A | — | likely benign |
| rs61746980 | 15:69,548,393 | A/G | — | benign |
| rs2548439873 | 15:69,548,584 | G/A | — | uncertain significance |
| rs2548444674 | 15:69,553,510 | A/G | — | uncertain significance |
| rs1295345242 | 15:69,553,599 | A/C | — | uncertain significance |
| rs11854180 | 15:69,559,340 | G/C | — | — |
| rs201600362 | 15:69,560,760 | G/T | — | uncertain significance |
| rs200073303 | 15:69,560,832 | A/T | — | uncertain significance |
| rs140697904 | 15:69,560,860 | C/G | — | benign |
| rs201612284 | 15:69,560,919 | C/G | — | uncertain significance |
| rs763256189 | 15:69,561,077 | G/A | — | uncertain significance |
| rs199559391 | 15:69,561,086 | A/G | — | uncertain significance |
| rs755045788 | 15:69,561,087 | C/T | — | uncertain significance |
| rs370173373 | 15:69,561,180 | A/G | — | uncertain significance |
| rs2548453826 | 15:69,561,278 | A/C | — | uncertain significance |
| rs2548454097 | 15:69,561,396 | C/T | — | uncertain significance |
| rs3865014 | 15:69,561,518 | G/C | missense variant | — |
| rs138450053 | 15:69,561,564 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.