AMER2
APC membrane recruitment protein 2
Summary
Enables phosphatidylinositol-4,5-bisphosphate binding activity. Involved in negative regulation of canonical Wnt signaling pathway. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs931992607 | 13:25,743,825 | G/C | — | uncertain significance |
| rs200341589 | 13:25,743,908 | T/C | — | uncertain significance |
| rs1314158849 | 13:25,743,986 | G/A | — | uncertain significance |
| rs756833733 | 13:25,744,010 | C/T | — | uncertain significance |
| rs1956530360 | 13:25,744,011 | G/A | — | uncertain significance |
| rs138356422 | 13:25,744,034 | T/C | — | uncertain significance |
| rs35077647 | 13:25,744,055 | G/A | — | uncertain significance |
| rs2541424040 | 13:25,744,124 | A/G | — | uncertain significance |
| rs1203169511 | 13:25,744,130 | G/A | — | uncertain significance |
| rs771130477 | 13:25,744,172 | G/A | — | uncertain significance |
| rs372214037 | 13:25,744,275 | G/A | — | uncertain significance |
| rs745917318 | 13:25,744,282 | C/A | — | uncertain significance |
| rs772062313 | 13:25,744,305 | C/T | — | uncertain significance |
| rs372051684 | 13:25,744,370 | G/T | — | uncertain significance |
| rs973676525 | 13:25,744,468 | C/G | — | uncertain significance |
| rs755019524 | 13:25,744,473 | C/T | — | uncertain significance |
| rs779014352 | 13:25,744,483 | C/T | — | uncertain significance |
| rs377253214 | 13:25,744,584 | C/A | — | uncertain significance |
| rs201615060 | 13:25,744,626 | G/T | — | uncertain significance |
| rs773799706 | 13:25,744,674 | T/C | — | uncertain significance |
| rs779988402 | 13:25,744,725 | C/T | — | uncertain significance |
| rs955478495 | 13:25,744,829 | G/A | — | uncertain significance |
| rs2541426973 | 13:25,744,883 | T/C | — | uncertain significance |
| rs765077387 | 13:25,744,914 | G/C | — | uncertain significance |
| rs780402695 | 13:25,744,964 | C/A | — | uncertain significance |
| rs373339623 | 13:25,745,007 | G/A | — | uncertain significance |
| rs373180945 | 13:25,745,102 | G/A | — | uncertain significance |
| rs1399161313 | 13:25,745,106 | G/C | — | uncertain significance |
| rs577045065 | 13:25,745,118 | C/G | — | uncertain significance |
| rs765793824 | 13:25,745,159 | C/T | — | uncertain significance |
| rs150291859 | 13:25,745,208 | T/C | — | uncertain significance |
| rs200352589 | 13:25,745,286 | C/G | — | uncertain significance |
| rs767856873 | 13:25,745,463 | C/T | — | uncertain significance |
| rs891375832 | 13:25,745,501 | A/G | — | uncertain significance |
| rs201888731 | 13:25,745,550 | A/C | — | uncertain significance |
| rs753516298 | 13:25,745,649 | C/T | — | uncertain significance |
| rs760756687 | 13:25,745,679 | T/C | — | uncertain significance |
| rs969047023 | 13:25,745,730 | C/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.