EPB41L2
erythrocyte membrane protein band 4.1 like 2
Summary
Predicted to enable PH domain binding activity; cytoskeletal protein binding activity; and structural molecule activity. Involved in positive regulation of protein localization to cell cortex. Located in several cellular components, including cell cortex; cell junction; and nucleus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants85 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs138876669 | 6:131,162,341 | A/G | downstream gene variant | — |
| rs750629350 | 6:131,179,334 | G/A | — | uncertain significance |
| rs924698049 | 6:131,184,784 | A/C | — | uncertain significance |
| rs1411736024 | 6:131,184,810 | T/C | — | uncertain significance |
| rs373063956 | 6:131,184,830 | C/A | — | uncertain significance |
| rs1450845776 | 6:131,184,845 | C/T | — | uncertain significance |
| rs1285393819 | 6:131,184,846 | C/T | — | uncertain significance |
| rs7770860 | 6:131,186,393 | T/C | intron variant | — |
| rs199859070 | 6:131,186,698 | G/A | — | uncertain significance |
| rs753806085 | 6:131,186,738 | G/C | — | uncertain significance |
| rs749789634 | 6:131,186,765 | C/T | — | uncertain significance |
| rs141483573 | 6:131,190,760 | G/A | — | benign |
| rs1451273055 | 6:131,190,776 | T/A | — | uncertain significance |
| rs150873575 | 6:131,190,813 | C/T | — | uncertain significance |
| rs745805908 | 6:131,190,820 | G/C | — | uncertain significance |
| rs779872725 | 6:131,190,822 | G/A | — | uncertain significance |
| rs761611852 | 6:131,190,837 | C/T | — | uncertain significance |
| rs1183796619 | 6:131,190,860 | T/C | — | uncertain significance |
| rs1415892992 | 6:131,190,861 | T/C | — | uncertain significance |
| rs200766051 | 6:131,190,924 | C/T | — | uncertain significance |
| rs147524336 | 6:131,190,965 | C/T | — | uncertain significance |
| rs776044538 | 6:131,190,966 | G/A | — | uncertain significance |
| rs565716598 | 6:131,191,020 | C/T | — | uncertain significance |
| rs539745210 | 6:131,191,028 | C/T | — | uncertain significance |
| rs748999213 | 6:131,191,053 | C/T | — | uncertain significance |
| rs201873243 | 6:131,191,071 | C/G | — | uncertain significance |
| rs145332499 | 6:131,191,080 | T/C | — | uncertain significance |
| rs375869610 | 6:131,191,082 | C/A | — | uncertain significance |
| rs376210129 | 6:131,191,083 | T/A | — | uncertain significance |
| rs554992186 | 6:131,191,140 | G/A | — | uncertain significance |
| rs767470524 | 6:131,191,185 | T/C | — | uncertain significance |
| rs753274531 | 6:131,191,226 | C/T | — | likely benign |
| rs778365462 | 6:131,191,260 | G/A | — | uncertain significance |
| rs2482757935 | 6:131,191,266 | T/C | — | uncertain significance |
| rs1571911 | 6:131,193,946 | C/A | — | — |
| rs529204084 | 6:131,195,978 | T/C | — | — |
| rs145209176 | 6:131,199,345 | T/C | — | uncertain significance |
| rs1462944699 | 6:131,199,383 | T/C | — | uncertain significance |
| rs200832085 | 6:131,201,333 | C/G | — | uncertain significance |
| rs977302461 | 6:131,206,257 | A/T | — | uncertain significance |
| rs200447334 | 6:131,206,292 | T/C | — | uncertain significance |
| rs766192220 | 6:131,206,310 | C/T | — | uncertain significance |
| rs1305269816 | 6:131,206,328 | G/A | — | uncertain significance |
| rs140741017 | 6:131,206,343 | C/T | — | uncertain significance |
| rs76682195 | 6:131,206,405 | G/A | — | benign |
| rs202041604 | 6:131,211,518 | G/A | — | uncertain significance |
| rs375639120 | 6:131,216,141 | C/T | — | uncertain significance |
| rs528595903 | 6:131,216,237 | T/C | — | uncertain significance |
| rs375573893 | 6:131,220,658 | C/T | — | uncertain significance |
| rs142296383 | 6:131,220,689 | T/C | — | uncertain significance |
| rs117767635 | 6:131,222,232 | T/C | — | uncertain significance |
| rs1562438245 | 6:131,222,240 | C/T | — | uncertain significance |
| rs1489925865 | 6:131,222,286 | C/A | — | uncertain significance |
| rs781423429 | 6:131,225,629 | G/A | — | uncertain significance |
| rs752476299 | 6:131,229,981 | T/C | — | uncertain significance |
| rs4897475 | 6:131,232,950 | A/T | — | — |
| rs11967564 | 6:131,235,859 | G/T | intron variant | — |
| rs1462680470 | 6:131,247,818 | T/C | — | uncertain significance |
| rs776286503 | 6:131,247,837 | C/G | — | uncertain significance |
| rs7769153 | 6:131,256,364 | T/G | regulatory region variant | — |
| rs375264771 | 6:131,276,265 | C/T | — | uncertain significance |
| rs780237457 | 6:131,276,294 | T/C | — | uncertain significance |
| rs2483322245 | 6:131,276,392 | T/G | — | uncertain significance |
| rs138467790 | 6:131,276,437 | C/A | — | uncertain significance |
| rs775029576 | 6:131,277,180 | G/A | — | uncertain significance |
| rs768324755 | 6:131,277,186 | T/C | — | uncertain significance |
| rs777267153 | 6:131,277,205 | C/G | — | uncertain significance |
| rs1300229260 | 6:131,277,310 | C/T | — | uncertain significance |
| rs2483344351 | 6:131,277,450 | A/G | — | likely benign |
| rs777437234 | 6:131,277,471 | G/A | — | uncertain significance |
| rs970257200 | 6:131,277,589 | T/C | — | uncertain significance |
| rs6941712 | 6:131,282,210 | T/A | — | — |
| rs201068830 | 6:131,287,179 | T/A | — | — |
| rs9375787 | 6:131,295,636 | G/T | — | — |
| rs9375788 | 6:131,299,147 | C/T | intron variant | — |
| rs9483203 | 6:131,309,869 | T/A | — | — |
| rs60215702 | 6:131,315,940 | G/C | regulatory region variant | — |
| rs6928878 | 6:131,344,906 | T/C | — | — |
| rs6908917 | 6:131,355,864 | G/T | — | — |
| rs7758016 | 6:131,365,376 | G/T | — | — |
| rs9492790 | 6:131,368,493 | A/C | intron variant | — |
| rs35250412 | 6:131,372,609 | C/A | — | — |
| rs9398971 | 6:131,378,927 | C/G | intron variant | — |
| rs6903705 | 6:131,379,667 | C/T | regulatory region variant | — |
| rs9483209 | 6:131,382,819 | C/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.