B3GNT8
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8
Summary
Enables protein N-acetylglucosaminyltransferase activity. Involved in poly-N-acetyllactosamine biosynthetic process. Located in extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants50 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs61443543 | 19:41,931,483 | A/G | — | benign |
| rs776693975 | 19:41,931,503 | C/T | — | uncertain significance |
| rs765230120 | 19:41,931,518 | T/G | — | uncertain significance |
| rs138916717 | 19:41,931,557 | C/T | — | uncertain significance |
| rs1480679266 | 19:41,931,567 | G/T | — | uncertain significance |
| rs762307853 | 19:41,931,600 | G/A | — | uncertain significance |
| rs142785792 | 19:41,931,605 | G/T | — | uncertain significance |
| rs1451683221 | 19:41,931,621 | G/A | — | uncertain significance |
| rs375027923 | 19:41,931,641 | G/A | — | uncertain significance |
| rs768060232 | 19:41,931,642 | G/A | — | uncertain significance |
| rs867883526 | 19:41,931,696 | A/G | — | uncertain significance |
| rs139702020 | 19:41,931,707 | C/T | — | uncertain significance |
| rs749519743 | 19:41,931,708 | G/A | — | uncertain significance |
| rs200756754 | 19:41,931,720 | G/A | — | uncertain significance |
| rs540476064 | 19:41,931,741 | G/A | — | uncertain significance |
| rs562080714 | 19:41,931,744 | C/T | — | uncertain significance |
| rs118127028 | 19:41,931,754 | G/A | — | benign |
| rs370096077 | 19:41,931,851 | G/A | — | uncertain significance |
| rs763742733 | 19:41,931,903 | G/A | — | uncertain significance |
| rs372925805 | 19:41,931,953 | C/T | — | likely benign |
| rs2513464268 | 19:41,931,956 | A/G | — | uncertain significance |
| rs367564055 | 19:41,931,960 | C/G | — | uncertain significance |
| rs1599967364 | 19:41,931,993 | A/G | — | uncertain significance |
| rs45563938 | 19:41,932,063 | A/G | — | benign |
| rs284660 | 19:41,932,084 | T/G | — | benign |
| rs284661 | 19:41,932,120 | C/T | — | benign |
| rs284662 | 19:41,932,275 | C/T | — | benign |
| rs145254457 | 19:41,932,291 | C/T | — | benign |
| rs571571024 | 19:41,932,311 | G/A | — | uncertain significance |
| rs2513464725 | 19:41,932,313 | C/A | — | uncertain significance |
| rs768710783 | 19:41,932,334 | C/T | — | uncertain significance |
| rs554231697 | 19:41,932,335 | G/T | — | uncertain significance |
| rs763498174 | 19:41,932,350 | G/A | — | uncertain significance |
| rs1036917595 | 19:41,932,372 | C/A | — | uncertain significance |
| rs774886863 | 19:41,932,406 | C/T | — | likely benign |
| rs373910300 | 19:41,932,412 | G/A | — | uncertain significance |
| rs765847100 | 19:41,932,429 | A/C | — | uncertain significance |
| rs2039438294 | 19:41,932,430 | C/T | — | uncertain significance |
| rs573401443 | 19:41,932,448 | C/T | — | uncertain significance |
| rs142245951 | 19:41,932,474 | A/C | — | uncertain significance |
| rs2039439037 | 19:41,932,475 | A/C | — | uncertain significance |
| rs371855817 | 19:41,932,521 | G/A | — | uncertain significance |
| rs200740953 | 19:41,932,552 | G/T | — | uncertain significance |
| rs2513465137 | 19:41,932,577 | G/A | — | uncertain significance |
| rs140645718 | 19:41,932,602 | C/T | — | uncertain significance |
| rs284663 | 19:41,932,612 | C/T | — | benign |
| rs368726896 | 19:41,932,659 | A/T | — | uncertain significance |
| rs45623740 | 19:41,932,758 | T/C | — | benign |
| rs45491295 | 19:41,932,828 | G/A | — | benign |
| rs115175314 | 19:41,932,963 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.