MAN2A2
mannosidase alpha class 2A member 2
Summary
Predicted to enable alpha-mannosidase activity. Predicted to be involved in N-glycan processing. Predicted to be located in Golgi apparatus and membrane. Predicted to be active in Golgi membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants83 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2677743 | 15:91,447,509 | C/T | — | benign |
| rs779168195 | 15:91,448,560 | T/G | — | uncertain significance |
| rs138296704 | 15:91,448,591 | C/A | — | uncertain significance |
| rs1003959385 | 15:91,448,701 | T/G | — | uncertain significance |
| rs372591005 | 15:91,448,715 | C/T | — | uncertain significance |
| rs200739221 | 15:91,448,716 | G/A | — | uncertain significance |
| rs150577814 | 15:91,448,719 | G/T | — | uncertain significance |
| rs201540535 | 15:91,448,809 | A/G | — | uncertain significance |
| rs139658442 | 15:91,448,813 | T/C | — | uncertain significance |
| rs2034218198 | 15:91,448,872 | T/C | — | uncertain significance |
| rs751761060 | 15:91,448,875 | G/A | — | uncertain significance |
| rs374688808 | 15:91,448,896 | G/A | — | uncertain significance |
| rs369589002 | 15:91,449,168 | G/A | — | uncertain significance |
| rs200666844 | 15:91,449,234 | C/G | — | uncertain significance |
| rs149181282 | 15:91,449,612 | C/G | — | uncertain significance |
| rs374359568 | 15:91,449,629 | C/T | — | uncertain significance |
| rs2542911173 | 15:91,449,721 | A/C | — | uncertain significance |
| rs141242339 | 15:91,449,982 | G/A | — | uncertain significance |
| rs1327432377 | 15:91,450,061 | G/A | — | uncertain significance |
| rs1471608021 | 15:91,450,112 | C/A | — | uncertain significance |
| rs2677744 | 15:91,450,441 | G/C | — | — |
| rs368969435 | 15:91,450,542 | C/T | — | uncertain significance |
| rs747910439 | 15:91,450,650 | G/A | — | uncertain significance |
| rs771890334 | 15:91,450,665 | G/A | — | uncertain significance |
| rs201233240 | 15:91,450,695 | G/A | — | uncertain significance |
| rs138305875 | 15:91,452,553 | C/G | — | likely benign |
| rs2106673 | 15:91,452,595 | A/G | — | benign |
| rs139423177 | 15:91,452,604 | G/A | — | uncertain significance |
| rs760909612 | 15:91,452,629 | T/G | — | likely benign |
| rs765804428 | 15:91,452,669 | G/A | — | uncertain significance |
| rs2542952497 | 15:91,453,323 | C/A | — | uncertain significance |
| rs753174851 | 15:91,453,771 | C/T | — | uncertain significance |
| rs778476492 | 15:91,453,774 | C/T | — | uncertain significance |
| rs141175483 | 15:91,453,790 | G/C | — | uncertain significance |
| rs911783007 | 15:91,453,831 | C/T | — | uncertain significance |
| rs77433391 | 15:91,454,110 | C/T | — | benign |
| rs142815948 | 15:91,454,168 | C/T | — | uncertain significance |
| rs143417684 | 15:91,454,441 | C/T | — | uncertain significance |
| rs757444506 | 15:91,454,677 | A/G | — | likely benign |
| rs150751359 | 15:91,454,686 | G/A | — | uncertain significance |
| rs377597565 | 15:91,454,691 | C/A | — | uncertain significance |
| rs777498221 | 15:91,454,754 | A/G | — | uncertain significance |
| rs145725923 | 15:91,454,757 | G/A | — | uncertain significance |
| rs771045586 | 15:91,455,288 | C/T | — | uncertain significance |
| rs74039150 | 15:91,455,321 | C/T | — | benign |
| rs141325951 | 15:91,455,345 | C/T | — | uncertain significance |
| rs138188731 | 15:91,455,349 | C/T | — | uncertain significance |
| rs2034803422 | 15:91,455,384 | C/T | — | uncertain significance |
| rs190876095 | 15:91,455,424 | G/A | — | uncertain significance |
| rs756269003 | 15:91,455,447 | G/A | — | uncertain significance |
| rs200668237 | 15:91,455,466 | G/A | — | uncertain significance |
| rs765886932 | 15:91,455,473 | G/A | — | uncertain significance |
| rs758677234 | 15:91,455,783 | G/T | — | uncertain significance |
| rs147693148 | 15:91,455,835 | A/G | — | uncertain significance |
| rs551769619 | 15:91,456,120 | A/G | — | uncertain significance |
| rs761132723 | 15:91,456,131 | G/A | — | uncertain significance |
| rs1266491 | 15:91,456,173 | G/A | — | uncertain significance |
| rs746738031 | 15:91,456,174 | C/T | — | conflicting classifications of pathogenicity |
| rs199738733 | 15:91,456,562 | A/C | — | uncertain significance |
| rs1596166404 | 15:91,456,587 | C/A | — | uncertain significance |
| rs773866909 | 15:91,456,595 | G/A | — | uncertain significance |
| rs2542999802 | 15:91,456,613 | T/G | — | uncertain significance |
| rs189268169 | 15:91,456,859 | T/C | — | uncertain significance |
| rs764927109 | 15:91,456,877 | C/G | — | uncertain significance |
| rs775378947 | 15:91,456,980 | A/G | — | uncertain significance |
| rs2543026491 | 15:91,459,410 | G/A | — | uncertain significance |
| rs748948156 | 15:91,459,422 | A/G | — | uncertain significance |
| rs778831892 | 15:91,459,437 | C/T | — | uncertain significance |
| rs570887330 | 15:91,459,451 | C/T | — | uncertain significance |
| rs777153370 | 15:91,459,452 | G/A | — | uncertain significance |
| rs372172477 | 15:91,459,466 | C/T | — | uncertain significance |
| rs751820500 | 15:91,459,472 | A/T | — | uncertain significance |
| rs373417566 | 15:91,461,497 | C/G | — | uncertain significance |
| rs369185701 | 15:91,461,524 | A/T | — | uncertain significance |
| rs374790154 | 15:91,461,891 | C/T | — | uncertain significance |
| rs758376776 | 15:91,461,894 | C/T | — | likely benign |
| rs776525016 | 15:91,461,902 | G/A | — | uncertain significance |
| rs370462457 | 15:91,461,918 | G/A | — | uncertain significance |
| rs147904374 | 15:91,461,945 | C/A | — | uncertain significance |
| rs1008378128 | 15:91,462,889 | G/A | — | uncertain significance |
| rs145619805 | 15:91,462,967 | G/A | — | likely benign |
| rs143436965 | 15:91,463,000 | C/T | — | uncertain significance |
| rs753017838 | 15:91,463,012 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.