MGAT5B
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B
Summary
Enables alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase activity and manganese ion binding activity. Involved in protein O-linked glycosylation via serine. Predicted to be located in Golgi membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants48 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1317406791 | 17:74,865,145 | G/C | — | uncertain significance |
| rs376875305 | 17:74,868,878 | G/A | — | uncertain significance |
| rs191831149 | 17:74,868,887 | C/T | — | likely benign |
| rs1396587792 | 17:74,868,946 | G/A | — | uncertain significance |
| rs776468880 | 17:74,878,254 | G/A | — | uncertain significance |
| rs765152905 | 17:74,878,256 | G/A | — | uncertain significance |
| rs763139701 | 17:74,878,275 | G/A | — | uncertain significance |
| rs776718727 | 17:74,878,301 | C/T | — | uncertain significance |
| rs377057899 | 17:74,878,302 | G/A | — | uncertain significance |
| rs1598897519 | 17:74,878,311 | C/T | — | uncertain significance |
| rs780552431 | 17:74,878,347 | G/A | — | uncertain significance |
| rs755042513 | 17:74,878,355 | G/A | — | uncertain significance |
| rs770937816 | 17:74,878,365 | A/G | — | uncertain significance |
| rs768175679 | 17:74,898,641 | C/G | — | uncertain significance |
| rs142179833 | 17:74,898,666 | G/A | — | uncertain significance |
| rs765506580 | 17:74,898,689 | G/A | — | uncertain significance |
| rs746182316 | 17:74,898,725 | C/T | — | uncertain significance |
| rs964424143 | 17:74,899,435 | C/T | — | uncertain significance |
| rs1046291792 | 17:74,900,446 | T/C | — | uncertain significance |
| rs62080221 | 17:74,901,330 | G/A | — | uncertain significance |
| rs200952928 | 17:74,901,372 | G/A | — | uncertain significance |
| rs758394238 | 17:74,902,142 | G/A | — | uncertain significance |
| rs138534156 | 17:74,902,205 | C/A | — | uncertain significance |
| rs1968519213 | 17:74,902,211 | G/A | — | uncertain significance |
| rs114240204 | 17:74,921,063 | G/A | — | likely benign |
| rs771745922 | 17:74,921,070 | C/T | — | uncertain significance |
| rs140434997 | 17:74,921,071 | G/A | — | uncertain significance |
| rs768725251 | 17:74,921,073 | G/A | — | uncertain significance |
| rs2509702266 | 17:74,921,078 | C/A | — | uncertain significance |
| rs537970370 | 17:74,921,106 | G/A | — | uncertain significance |
| rs912752305 | 17:74,922,698 | G/A | — | uncertain significance |
| rs185413190 | 17:74,922,758 | C/T | — | uncertain significance |
| rs767094719 | 17:74,928,781 | C/T | — | uncertain significance |
| rs4789378 | 17:74,930,366 | T/C | intron variant | — |
| rs1969732755 | 17:74,934,106 | A/G | — | uncertain significance |
| rs776224034 | 17:74,934,145 | C/A | — | uncertain significance |
| rs975235635 | 17:74,936,490 | A/G | — | uncertain significance |
| rs199872537 | 17:74,936,836 | C/T | — | uncertain significance |
| rs35895146 | 17:74,936,849 | C/T | — | likely benign |
| rs192072696 | 17:74,940,695 | A/G | intron variant | — |
| rs1970030553 | 17:74,942,463 | C/A | — | uncertain significance |
| rs140485620 | 17:74,943,954 | G/A | — | likely benign |
| rs1970082914 | 17:74,943,965 | C/A | — | uncertain significance |
| rs577829864 | 17:74,944,057 | G/A | — | uncertain significance |
| rs754899240 | 17:74,944,070 | C/T | — | likely benign |
| rs146879660 | 17:74,944,074 | C/T | — | uncertain significance |
| rs201168609 | 17:74,944,092 | G/A | — | uncertain significance |
| rs565431949 | 17:74,944,177 | T/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.