GLT8D2
glycosyltransferase 8 domain containing 2
Summary
Predicted to enable UDP-glycosyltransferase activity. Predicted to be located in membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs767185474 | 12:104,383,331 | G/A | — | uncertain significance |
| rs4135150 | 12:104,383,599 | T/C | downstream gene variant | — |
| rs2540781878 | 12:104,387,193 | G/C | — | uncertain significance |
| rs145520946 | 12:104,387,233 | T/C | missense variant | — |
| rs1212627359 | 12:104,387,265 | C/G | — | uncertain significance |
| rs372103586 | 12:104,387,282 | C/G | — | uncertain significance |
| rs375188513 | 12:104,388,128 | A/G | — | uncertain significance |
| rs1332176405 | 12:104,388,138 | C/T | — | uncertain significance |
| rs201963804 | 12:104,388,247 | C/G | — | uncertain significance |
| rs200518430 | 12:104,388,248 | T/C | — | uncertain significance |
| rs2540786332 | 12:104,388,249 | T/C | — | uncertain significance |
| rs148318774 | 12:104,388,252 | G/A | — | uncertain significance |
| rs754516562 | 12:104,388,275 | G/A | — | uncertain significance |
| rs149453281 | 12:104,390,601 | G/T | — | uncertain significance |
| rs1292773688 | 12:104,391,236 | A/C | — | uncertain significance |
| rs202210738 | 12:104,391,279 | A/G | — | uncertain significance |
| rs375188988 | 12:104,393,178 | C/G | — | uncertain significance |
| rs369320125 | 12:104,396,934 | C/T | — | uncertain significance |
| rs2540816280 | 12:104,397,003 | G/C | — | uncertain significance |
| rs1311519167 | 12:104,397,039 | A/G | — | uncertain significance |
| rs117801489 | 12:104,408,832 | T/C | missense variant | — |
| rs143981260 | 12:104,408,838 | A/G | — | uncertain significance |
| rs149081888 | 12:104,416,712 | A/T | intron variant | — |
| rs2629751 | 12:104,421,808 | A/G | upstream gene variant | — |
| rs1564892 | 12:104,445,742 | A/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.