B4GALNT4
beta-1,4-N-acetyl-galactosaminyltransferase 4
Summary
Enables acetylgalactosaminyltransferase activity. Predicted to be located in Golgi cisterna membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants81 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs892200851 | 11:369,948 | G/C | — | uncertain significance |
| rs76560824 | 11:370,252 | T/C | regulatory region variant | — |
| rs753662463 | 11:372,126 | A/G | — | likely benign |
| rs748055483 | 11:372,148 | T/C | — | uncertain significance |
| rs916966978 | 11:372,153 | G/A | — | uncertain significance |
| rs1846629650 | 11:372,207 | C/A | — | uncertain significance |
| rs747752780 | 11:372,211 | C/T | — | likely benign |
| rs1389772829 | 11:372,696 | G/C | — | likely benign |
| rs200752314 | 11:373,027 | C/T | — | uncertain significance |
| rs115266356 | 11:373,061 | C/T | — | benign |
| rs2539232555 | 11:373,265 | G/T | — | uncertain significance |
| rs2539232592 | 11:373,286 | G/A | — | not provided |
| rs756387996 | 11:373,763 | C/T | — | uncertain significance |
| rs201282450 | 11:375,531 | C/T | — | not provided |
| rs1293010642 | 11:375,673 | C/G | — | uncertain significance |
| rs151090425 | 11:375,698 | G/A | — | uncertain significance |
| rs118028728 | 11:375,701 | G/A | — | uncertain significance |
| rs1363430302 | 11:375,715 | G/C | — | likely benign |
| rs201266689 | 11:375,716 | C/A | — | uncertain significance |
| rs200374914 | 11:375,780 | G/A | — | benign |
| rs773270181 | 11:375,861 | T/C | — | likely benign |
| rs375662614 | 11:375,872 | G/A | — | likely benign |
| rs762669988 | 11:375,889 | C/G | — | uncertain significance |
| rs751107435 | 11:375,900 | G/A | — | uncertain significance |
| rs767066411 | 11:375,910 | A/G | — | uncertain significance |
| rs1846737093 | 11:375,926 | C/A | — | uncertain significance |
| rs777908097 | 11:375,934 | C/T | — | uncertain significance |
| rs1846743201 | 11:376,093 | A/T | — | uncertain significance |
| rs750624114 | 11:376,159 | C/T | — | uncertain significance |
| rs201456025 | 11:376,268 | A/T | — | uncertain significance |
| rs759704935 | 11:376,291 | G/A | — | uncertain significance |
| rs779593944 | 11:376,315 | G/A | — | uncertain significance |
| rs937595434 | 11:376,330 | T/C | — | uncertain significance |
| rs111622783 | 11:376,343 | A/G | — | benign |
| rs1846756929 | 11:376,502 | A/C | — | likely benign |
| rs1286215919 | 11:376,546 | G/A | — | uncertain significance |
| rs1030412585 | 11:376,550 | C/T | — | uncertain significance |
| rs539165548 | 11:376,553 | C/G | — | uncertain significance |
| rs558666429 | 11:376,571 | G/A | — | uncertain significance |
| rs1846759504 | 11:376,580 | G/A | — | uncertain significance |
| rs1291522819 | 11:376,583 | C/A | — | uncertain significance |
| rs762727549 | 11:376,588 | A/G | — | uncertain significance |
| rs761643991 | 11:376,637 | C/G | — | uncertain significance |
| rs1846764094 | 11:376,732 | T/G | — | uncertain significance |
| rs1260850619 | 11:376,765 | C/T | — | uncertain significance |
| rs902499502 | 11:376,840 | C/G | — | uncertain significance |
| rs757315346 | 11:376,864 | G/A | — | uncertain significance |
| rs1283620054 | 11:376,867 | C/T | — | uncertain significance |
| rs2539242809 | 11:376,933 | G/T | — | uncertain significance |
| rs749728221 | 11:376,934 | C/T | — | uncertain significance |
| rs984303735 | 11:376,940 | C/A | — | uncertain significance |
| rs772756363 | 11:376,981 | T/G | — | uncertain significance |
| rs368506284 | 11:377,023 | G/A | — | uncertain significance |
| rs751769045 | 11:377,073 | G/T | — | likely benign |
| rs1044925374 | 11:377,083 | G/A | — | uncertain significance |
| rs952346192 | 11:377,114 | G/A | — | uncertain significance |
| rs1208212214 | 11:377,125 | G/A | — | uncertain significance |
| rs770437353 | 11:377,150 | G/C | — | uncertain significance |
| rs2539243443 | 11:377,161 | A/G | — | uncertain significance |
| rs780611005 | 11:377,270 | C/T | — | uncertain significance |
| rs750103769 | 11:379,425 | G/T | — | uncertain significance |
| rs778846368 | 11:379,458 | C/T | — | uncertain significance |
| rs996140395 | 11:379,552 | G/C | — | uncertain significance |
| rs1846830519 | 11:379,633 | G/A | — | uncertain significance |
| rs969948443 | 11:379,657 | G/T | — | uncertain significance |
| rs758407647 | 11:379,682 | G/A | — | uncertain significance |
| rs762470791 | 11:379,895 | T/A | — | uncertain significance |
| rs750284296 | 11:379,920 | A/G | — | uncertain significance |
| rs1846838451 | 11:379,934 | G/T | — | uncertain significance |
| rs956946168 | 11:379,940 | C/T | — | uncertain significance |
| rs142922840 | 11:379,948 | C/T | — | likely benign |
| rs201217686 | 11:379,973 | G/A | — | uncertain significance |
| rs371372220 | 11:380,292 | G/A | — | uncertain significance |
| rs2539248212 | 11:380,317 | G/A | — | uncertain significance |
| rs146988005 | 11:380,393 | C/T | — | likely benign |
| rs1215117474 | 11:380,403 | G/A | — | uncertain significance |
| rs768880532 | 11:380,436 | G/A | — | uncertain significance |
| rs377575836 | 11:380,904 | G/C | — | uncertain significance |
| rs966620721 | 11:381,703 | C/T | — | uncertain significance |
| rs202077321 | 11:381,758 | G/A | — | uncertain significance |
| rs376317908 | 11:381,775 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.