AMER3
APC membrane recruitment protein 3
Summary
Predicted to enable beta-catenin binding activity and phosphatidylinositol-4,5-bisphosphate binding activity. Predicted to be involved in regulation of canonical Wnt signaling pathway. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Apr 2025]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs147611031 | 2:131,519,659 | G/C | — | uncertain significance |
| rs772482449 | 2:131,519,714 | C/G | — | uncertain significance |
| rs754027088 | 2:131,519,766 | C/G | — | uncertain significance |
| rs2467382422 | 2:131,519,793 | G/A | — | uncertain significance |
| rs775305041 | 2:131,519,914 | G/A | — | uncertain significance |
| rs773354637 | 2:131,519,941 | C/T | — | uncertain significance |
| rs1558966402 | 2:131,519,944 | G/C | — | uncertain significance |
| rs529382254 | 2:131,520,015 | C/T | — | uncertain significance |
| rs753191925 | 2:131,520,018 | C/T | — | uncertain significance |
| rs200965524 | 2:131,520,033 | C/T | — | uncertain significance |
| rs141992347 | 2:131,520,034 | G/A | — | uncertain significance |
| rs149619600 | 2:131,520,045 | C/G | — | uncertain significance |
| rs749518900 | 2:131,520,056 | C/T | — | likely benign |
| rs774400302 | 2:131,520,076 | A/G | — | uncertain significance |
| rs147594621 | 2:131,520,145 | G/A | — | uncertain significance |
| rs749142142 | 2:131,520,154 | A/C | — | uncertain significance |
| rs772346033 | 2:131,520,169 | C/T | — | uncertain significance |
| rs936279743 | 2:131,520,180 | G/A | — | likely benign |
| rs201307390 | 2:131,520,183 | G/A | — | likely benign |
| rs200390810 | 2:131,520,190 | A/G | — | uncertain significance |
| rs1678828173 | 2:131,520,225 | G/T | — | uncertain significance |
| rs146781752 | 2:131,520,232 | G/A | — | likely benign |
| rs757646211 | 2:131,520,248 | C/G | — | uncertain significance |
| rs138907399 | 2:131,520,256 | C/T | — | likely benign |
| rs1678831192 | 2:131,520,271 | G/A | — | uncertain significance |
| rs200592484 | 2:131,520,297 | T/G | — | uncertain significance |
| rs376744972 | 2:131,520,318 | G/A | — | uncertain significance |
| rs756148572 | 2:131,520,321 | G/T | — | likely benign |
| rs749785896 | 2:131,520,333 | C/T | — | uncertain significance |
| rs774360975 | 2:131,520,487 | G/A | — | uncertain significance |
| rs1678844720 | 2:131,520,565 | C/T | — | uncertain significance |
| rs750932360 | 2:131,520,603 | C/G | — | uncertain significance |
| rs1426984937 | 2:131,520,609 | C/T | — | uncertain significance |
| rs200166860 | 2:131,520,678 | G/T | — | uncertain significance |
| rs767986216 | 2:131,520,690 | G/C | — | uncertain significance |
| rs753138909 | 2:131,520,754 | G/A | — | uncertain significance |
| rs952410383 | 2:131,520,775 | C/T | — | uncertain significance |
| rs2104782593 | 2:131,520,883 | C/T | — | uncertain significance |
| rs375663702 | 2:131,520,885 | C/G | — | uncertain significance |
| rs764045425 | 2:131,520,927 | G/A | — | uncertain significance |
| rs1460586435 | 2:131,521,009 | C/T | — | uncertain significance |
| rs776499369 | 2:131,521,044 | G/A | — | uncertain significance |
| rs751793214 | 2:131,521,084 | G/A | — | uncertain significance |
| rs376443283 | 2:131,521,143 | A/T | — | uncertain significance |
| rs752803111 | 2:131,521,182 | C/T | — | uncertain significance |
| rs377036438 | 2:131,521,189 | G/T | — | uncertain significance |
| rs757763628 | 2:131,521,282 | G/C | — | uncertain significance |
| rs1399819903 | 2:131,521,294 | T/C | — | uncertain significance |
| rs377413500 | 2:131,521,314 | G/A | — | uncertain significance |
| rs778968534 | 2:131,521,380 | G/A | — | uncertain significance |
| rs775957307 | 2:131,521,383 | G/A | — | uncertain significance |
| rs150310404 | 2:131,521,447 | G/A | — | likely benign |
| rs774939208 | 2:131,521,497 | T/C | — | uncertain significance |
| rs190910148 | 2:131,521,534 | A/C | — | uncertain significance |
| rs752665531 | 2:131,521,701 | A/C | — | uncertain significance |
| rs555066961 | 2:131,521,732 | C/T | — | uncertain significance |
| rs773934949 | 2:131,521,753 | G/A | — | uncertain significance |
| rs562674707 | 2:131,521,771 | G/A | — | uncertain significance |
| rs768719549 | 2:131,521,881 | C/T | — | likely pathogenic |
| rs762936709 | 2:131,521,926 | G/A | — | likely benign |
| rs1678919263 | 2:131,521,935 | G/A | — | uncertain significance |
| rs1457311751 | 2:131,521,953 | G/A | — | uncertain significance |
| rs368377961 | 2:131,521,985 | G/C | — | uncertain significance |
| rs147451502 | 2:131,522,007 | G/A | — | likely benign |
| rs140869723 | 2:131,522,049 | C/T | — | uncertain significance |
| rs774672370 | 2:131,522,088 | C/G | — | uncertain significance |
| rs772231954 | 2:131,522,112 | G/A | — | uncertain significance |
| rs199770925 | 2:131,522,113 | G/C | — | uncertain significance |
| rs760682073 | 2:131,522,116 | G/C | — | uncertain significance |
| rs752266201 | 2:131,522,143 | G/A | — | uncertain significance |
| rs377081234 | 2:131,522,161 | G/A | — | likely benign |
| rs1192118634 | 2:131,522,226 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.