GALNTL5
polypeptide N-acetylgalactosaminyltransferase like 5
Summary
Predicted to enable metal ion binding activity and transferase activity. Involved in spermatid development. Predicted to be located in late endosome membrane. Predicted to be active in Golgi apparatus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants39 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2485983023 | 7:151,664,342 | C/T | — | likely benign |
| rs778846871 | 7:151,664,368 | T/A | — | uncertain significance |
| rs2485983286 | 7:151,664,426 | T/A | — | uncertain significance |
| rs1309352702 | 7:151,664,452 | G/A | — | uncertain significance |
| rs753441607 | 7:151,664,486 | T/A | — | uncertain significance |
| rs1436252286 | 7:151,664,497 | A/G | — | uncertain significance |
| rs2151939058 | 7:151,664,515 | C/A | — | uncertain significance |
| rs374944397 | 7:151,664,559 | T/C | — | likely benign |
| rs748173069 | 7:151,664,563 | G/A | — | uncertain significance |
| rs751846967 | 7:151,668,077 | A/C | — | uncertain significance |
| rs148273290 | 7:151,668,151 | G/C | — | benign |
| rs144786536 | 7:151,668,159 | T/C | — | benign |
| rs35629905 | 7:151,680,130 | A/G | — | benign |
| rs202056038 | 7:151,680,202 | A/G | — | uncertain significance |
| rs200812489 | 7:151,680,245 | A/G | — | likely benign |
| rs61729494 | 7:151,684,246 | G/A | — | uncertain significance |
| rs1018899832 | 7:151,684,247 | A/G | — | uncertain significance |
| rs75797831 | 7:151,684,294 | G/A | — | likely benign |
| rs61729482 | 7:151,684,325 | G/C | — | benign |
| rs576160676 | 7:151,693,583 | G/A | — | — |
| rs151275982 | 7:151,699,801 | G/C | — | uncertain significance |
| rs147840774 | 7:151,699,829 | G/T | — | uncertain significance |
| rs755106841 | 7:151,699,846 | T/C | — | uncertain significance |
| rs761732434 | 7:151,699,897 | T/C | — | uncertain significance |
| rs747204163 | 7:151,699,913 | T/C | — | uncertain significance |
| rs781454120 | 7:151,699,954 | G/A | — | uncertain significance |
| rs201570532 | 7:151,700,015 | T/C | — | uncertain significance |
| rs143054627 | 7:151,700,036 | C/T | — | likely benign |
| rs376699695 | 7:151,704,917 | C/T | — | uncertain significance |
| rs747623447 | 7:151,704,947 | G/A | — | uncertain significance |
| rs770166154 | 7:151,711,791 | G/C | — | uncertain significance |
| rs2081783615 | 7:151,711,796 | A/G | — | uncertain significance |
| rs200259198 | 7:151,711,823 | G/A | — | uncertain significance |
| rs146121314 | 7:151,716,747 | G/A | — | uncertain significance |
| rs267601426 | 7:151,716,776 | G/A | — | uncertain significance |
| rs764055192 | 7:151,716,791 | C/A | — | uncertain significance |
| rs149825214 | 7:151,716,792 | G/A | — | uncertain significance |
| rs142778679 | 7:151,716,810 | G/C | — | uncertain significance |
| rs145318235 | 7:151,716,849 | T/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.