POGLUT3
protein O-glucosyltransferase 3
Summary
Enables UDP-glucosyltransferase activity and UDP-xylosyltransferase activity. Involved in protein O-linked glycosylation via serine. Predicted to be located in endoplasmic reticulum lumen. Predicted to be active in endomembrane system. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs537424181 | 11:108,345,585 | T/A | — | uncertain significance |
| rs200020105 | 11:108,345,622 | G/A | — | uncertain significance |
| rs377123293 | 11:108,345,643 | G/A | — | uncertain significance |
| rs765345289 | 11:108,345,658 | T/A | — | uncertain significance |
| rs11212662 | 11:108,346,196 | G/T | — | — |
| rs2548111437 | 11:108,350,137 | T/G | — | uncertain significance |
| rs1004257660 | 11:108,350,159 | C/G | — | uncertain significance |
| rs531322305 | 11:108,350,192 | C/A | — | uncertain significance |
| rs766673796 | 11:108,351,954 | T/C | — | uncertain significance |
| rs988925701 | 11:108,352,016 | T/G | — | uncertain significance |
| rs200951518 | 11:108,352,029 | C/T | — | uncertain significance |
| rs2548113457 | 11:108,352,748 | T/G | — | uncertain significance |
| rs1390770289 | 11:108,352,772 | C/A | — | uncertain significance |
| rs10749918 | 11:108,354,874 | C/A | — | — |
| rs753354801 | 11:108,356,939 | T/G | — | uncertain significance |
| rs2548116778 | 11:108,356,950 | T/A | — | uncertain significance |
| rs778413475 | 11:108,356,955 | G/A | — | uncertain significance |
| rs371817425 | 11:108,356,978 | G/A | — | uncertain significance |
| rs1433595636 | 11:108,356,991 | T/C | — | likely benign |
| rs777630786 | 11:108,357,002 | T/C | — | uncertain significance |
| rs774832914 | 11:108,357,024 | C/A | — | uncertain significance |
| rs1229651509 | 11:108,357,125 | T/C | — | uncertain significance |
| rs781054972 | 11:108,357,135 | C/T | — | uncertain significance |
| rs72993806 | 11:108,359,689 | C/G | intron variant | — |
| rs11212676 | 11:108,361,578 | G/A | intron variant | — |
| rs377642857 | 11:108,361,709 | A/G | — | uncertain significance |
| rs374443735 | 11:108,361,752 | C/A | — | uncertain significance |
| rs2093612319 | 11:108,361,805 | C/T | — | uncertain significance |
| rs750568803 | 11:108,361,840 | C/T | — | uncertain significance |
| rs201659706 | 11:108,361,849 | T/A | — | uncertain significance |
| rs201124629 | 11:108,361,850 | C/T | — | uncertain significance |
| rs764968041 | 11:108,368,942 | T/C | — | uncertain significance |
| rs750601502 | 11:108,368,951 | C/T | — | uncertain significance |
| rs768050765 | 11:108,368,990 | C/G | — | uncertain significance |
| rs1297310409 | 11:108,369,002 | C/T | — | uncertain significance |
| rs745453712 | 11:108,369,009 | C/A | — | uncertain significance |
| rs768315204 | 11:108,369,026 | G/C | — | uncertain significance |
| rs751814190 | 11:108,369,030 | C/T | — | uncertain significance |
| rs886067156 | 11:108,369,048 | G/T | — | uncertain significance |
| rs763194109 | 11:108,369,087 | G/A | — | uncertain significance |
| rs74822968 | 11:108,369,173 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.