XXYLT1
xyloside xylosyltransferase 1
Summary
Enables magnesium ion binding activity; manganese ion binding activity; and xylosyl alpha-1,3-xylosyltransferase activity. Involved in O-glycan processing. Located in endoplasmic reticulum membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants43 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs748659464 | 3:194,790,458 | T/C | — | uncertain significance |
| rs1714692400 | 3:194,790,540 | G/T | — | uncertain significance |
| rs374676960 | 3:194,790,541 | T/G | — | uncertain significance |
| rs73890648 | 3:194,790,585 | C/T | — | benign |
| rs201238998 | 3:194,790,665 | T/C | — | uncertain significance |
| rs199782083 | 3:194,790,668 | C/T | — | uncertain significance |
| rs766217283 | 3:194,790,781 | G/C | — | uncertain significance |
| rs375309181 | 3:194,790,787 | G/A | — | uncertain significance |
| rs770779670 | 3:194,790,825 | C/A | — | uncertain significance |
| rs9837892 | 3:194,840,047 | T/A | — | — |
| rs2131877 | 3:194,858,374 | G/A | upstream gene variant | — |
| rs4677813 | 3:194,863,860 | T/C | upstream gene variant | — |
| rs376617200 | 3:194,877,200 | G/A | — | uncertain significance |
| rs779805397 | 3:194,877,218 | C/T | — | uncertain significance |
| rs754661420 | 3:194,877,223 | G/A | — | uncertain significance |
| rs372269605 | 3:194,877,256 | C/T | — | uncertain significance |
| rs745899989 | 3:194,877,257 | G/A | — | uncertain significance |
| rs7616009 | 3:194,881,756 | G/A | regulatory region variant | — |
| rs73063126 | 3:194,893,849 | A/G | intron variant | — |
| rs766604392 | 3:194,947,507 | C/G | — | uncertain significance |
| rs199897126 | 3:194,947,512 | C/T | — | uncertain significance |
| rs755038921 | 3:194,947,525 | G/C | — | uncertain significance |
| rs201345395 | 3:194,947,557 | G/A | — | uncertain significance |
| rs77485504 | 3:194,972,515 | A/C | intron variant | — |
| rs76960093 | 3:194,980,147 | C/T | regulatory region variant | — |
| rs372983273 | 3:194,991,337 | C/A | — | uncertain significance |
| rs1177528792 | 3:194,991,370 | G/T | — | uncertain significance |
| rs760685833 | 3:194,991,373 | G/A | — | uncertain significance |
| rs540548399 | 3:194,991,395 | G/C | — | uncertain significance |
| rs565205225 | 3:194,991,402 | G/A | — | uncertain significance |
| rs768729168 | 3:194,991,438 | T/G | — | uncertain significance |
| rs2474668851 | 3:194,991,442 | C/T | — | uncertain significance |
| rs1181885983 | 3:194,991,474 | A/G | — | uncertain significance |
| rs767027930 | 3:194,991,489 | T/C | — | uncertain significance |
| rs1185280977 | 3:194,991,567 | G/A | — | uncertain significance |
| rs1159637862 | 3:194,991,595 | C/A | — | uncertain significance |
| rs1434976609 | 3:194,991,600 | G/T | — | uncertain significance |
| rs759777972 | 3:194,991,685 | C/T | — | uncertain significance |
| rs1336867866 | 3:194,991,702 | A/T | — | uncertain significance |
| rs1031379788 | 3:194,991,711 | G/A | — | uncertain significance |
| rs767203236 | 3:194,991,714 | C/T | — | uncertain significance |
| rs1275133743 | 3:194,991,780 | A/G | — | uncertain significance |
| rs1335489676 | 3:194,991,781 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.