AMZ1
archaelysin family metallopeptidase 1
Summary
Predicted to enable metal ion binding activity and metallopeptidase activity. Predicted to be involved in proteolysis. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants77 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs146838251 | 7:2,722,819 | G/A | regulatory region variant | — |
| rs184601060 | 7:2,740,104 | G/T | — | uncertain significance |
| rs764658622 | 7:2,740,122 | G/A | — | uncertain significance |
| rs1787985937 | 7:2,740,141 | A/T | — | uncertain significance |
| rs555064289 | 7:2,740,142 | C/A | — | uncertain significance |
| rs2534440873 | 7:2,740,300 | A/C | — | uncertain significance |
| rs1215507221 | 7:2,740,329 | G/A | — | uncertain significance |
| rs753714123 | 7:2,740,384 | C/T | — | uncertain significance |
| rs73281175 | 7:2,740,896 | T/C | intron variant | — |
| rs1724889 | 7:2,741,021 | G/A | intron variant | — |
| rs545587786 | 7:2,742,371 | C/T | — | uncertain significance |
| rs2534455658 | 7:2,742,376 | G/A | — | uncertain significance |
| rs1191356349 | 7:2,742,388 | C/A | — | uncertain significance |
| rs762909854 | 7:2,742,449 | C/T | — | uncertain significance |
| rs773979262 | 7:2,742,493 | C/T | — | uncertain significance |
| rs761641656 | 7:2,742,494 | G/A | — | likely benign |
| rs1056739027 | 7:2,742,505 | A/G | — | uncertain significance |
| rs374699485 | 7:2,742,514 | C/T | — | uncertain significance |
| rs150929801 | 7:2,748,233 | T/A | — | uncertain significance |
| rs1583172032 | 7:2,748,256 | A/G | — | likely benign |
| rs1269523430 | 7:2,748,312 | C/A | — | uncertain significance |
| rs767911544 | 7:2,748,732 | C/T | — | uncertain significance |
| rs142146201 | 7:2,748,768 | G/A | — | likely benign |
| rs150799683 | 7:2,748,787 | T/C | — | likely benign |
| rs768491440 | 7:2,748,796 | C/T | — | uncertain significance |
| rs201597646 | 7:2,748,830 | G/T | — | uncertain significance |
| rs778091933 | 7:2,748,836 | G/C | — | uncertain significance |
| rs75195869 | 7:2,748,844 | G/C | — | benign |
| rs58748470 | 7:2,748,901 | G/C | intron variant | — |
| rs2534507835 | 7:2,749,304 | G/A | — | uncertain significance |
| rs372905267 | 7:2,749,347 | C/T | — | uncertain significance |
| rs369227918 | 7:2,749,360 | C/A | — | uncertain significance |
| rs374323243 | 7:2,749,361 | G/C | — | uncertain significance |
| rs139061616 | 7:2,749,364 | G/C | — | uncertain significance |
| rs138351044 | 7:2,749,373 | C/G | — | uncertain significance |
| rs149587010 | 7:2,749,374 | G/C | — | uncertain significance |
| rs764934837 | 7:2,749,410 | T/G | — | uncertain significance |
| rs947462018 | 7:2,749,433 | C/T | — | uncertain significance |
| rs148450778 | 7:2,749,437 | T/C | — | uncertain significance |
| rs756099596 | 7:2,751,976 | T/C | — | uncertain significance |
| rs61745221 | 7:2,751,987 | G/A | — | benign |
| rs1478603284 | 7:2,751,989 | T/C | — | uncertain significance |
| rs1247563427 | 7:2,752,010 | A/G | — | uncertain significance |
| rs375504050 | 7:2,752,045 | C/G | — | uncertain significance |
| rs75954840 | 7:2,752,053 | C/T | — | benign |
| rs61742582 | 7:2,752,065 | G/A | — | benign |
| rs760684570 | 7:2,752,088 | C/T | — | uncertain significance |
| rs148396842 | 7:2,752,096 | G/A | — | uncertain significance |
| rs2534530273 | 7:2,752,103 | G/A | — | uncertain significance |
| rs2534530972 | 7:2,752,142 | C/T | — | uncertain significance |
| rs770980663 | 7:2,752,151 | C/T | — | uncertain significance |
| rs147110889 | 7:2,752,155 | G/A | — | benign |
| rs1399068585 | 7:2,752,187 | C/T | — | uncertain significance |
| rs2534531818 | 7:2,752,195 | C/A | — | uncertain significance |
| rs148936052 | 7:2,752,196 | C/T | — | likely benign |
| rs1193793462 | 7:2,752,219 | G/A | — | uncertain significance |
| rs2534533274 | 7:2,752,319 | A/G | — | uncertain significance |
| rs143816381 | 7:2,752,322 | C/T | — | benign |
| rs111981479 | 7:2,752,330 | C/T | — | benign |
| rs1214126523 | 7:2,752,367 | G/A | — | uncertain significance |
| rs897169661 | 7:2,752,369 | C/G | — | uncertain significance |
| rs148177744 | 7:2,752,383 | C/A | — | likely benign |
| rs147940046 | 7:2,752,396 | G/A | — | uncertain significance |
| rs201069985 | 7:2,752,405 | C/T | — | uncertain significance |
| rs373301330 | 7:2,752,417 | G/A | — | uncertain significance |
| rs140063618 | 7:2,752,446 | G/C | — | uncertain significance |
| rs145687592 | 7:2,752,456 | C/T | — | likely benign |
| rs201142649 | 7:2,752,486 | C/G | — | uncertain significance |
| rs751613832 | 7:2,752,499 | G/T | — | uncertain significance |
| rs7797295 | 7:2,755,237 | G/T | — | — |
| rs4719648 | 7:2,756,832 | T/C | regulatory region variant | — |
| rs798557 | 7:2,758,982 | G/A | regulatory region variant | — |
| rs798555 | 7:2,759,473 | T/C | downstream gene variant | — |
| rs798554 | 7:2,759,795 | C/T | downstream gene variant | — |
| rs798545 | 7:2,762,386 | C/G | — | — |
| rs798544 | 7:2,763,102 | C/T | downstream gene variant | — |
| rs186172963 | 7:2,763,738 | G/C | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.