BCL9L
BCL9 like
Summary
Enables beta-catenin binding activity. Involved in several processes, including negative regulation of transforming growth factor beta receptor signaling pathway; positive regulation of epithelial to mesenchymal transition; and positive regulation of transcription by RNA polymerase II. Located in fibrillar center and nucleoplasm. Part of beta-catenin-TCF complex. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants126 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs368349675 | 11:118,769,147 | C/T | — | likely benign |
| rs770763108 | 11:118,769,201 | G/A | — | uncertain significance |
| rs2496666395 | 11:118,769,219 | T/G | — | uncertain significance |
| rs139914635 | 11:118,769,259 | C/T | — | benign |
| rs775555001 | 11:118,769,267 | G/A | — | uncertain significance |
| rs376830821 | 11:118,769,278 | G/A | — | uncertain significance |
| rs79654456 | 11:118,769,303 | C/T | — | benign |
| rs750301417 | 11:118,769,327 | A/T | — | uncertain significance |
| rs2496667797 | 11:118,769,369 | C/T | — | uncertain significance |
| rs2496668051 | 11:118,769,397 | C/G | — | uncertain significance |
| rs1419059462 | 11:118,769,408 | G/A | — | uncertain significance |
| rs7104819 | 11:118,769,442 | A/G | — | benign |
| rs2496668761 | 11:118,769,453 | T/C | — | uncertain significance |
| rs754986219 | 11:118,769,467 | C/T | — | uncertain significance |
| rs747500524 | 11:118,769,576 | G/A | — | uncertain significance |
| rs138738007 | 11:118,769,589 | G/A | — | benign |
| rs61751532 | 11:118,769,604 | T/C | — | benign |
| rs2496670504 | 11:118,769,605 | T/C | — | uncertain significance |
| rs745528653 | 11:118,769,648 | A/T | — | uncertain significance |
| rs773305789 | 11:118,769,669 | T/C | — | uncertain significance |
| rs199836573 | 11:118,769,699 | C/T | — | uncertain significance |
| rs779741410 | 11:118,769,705 | C/T | — | uncertain significance |
| rs1329125389 | 11:118,769,710 | A/G | — | uncertain significance |
| rs2496671716 | 11:118,769,731 | A/G | — | uncertain significance |
| rs771126846 | 11:118,769,750 | C/T | — | likely benign |
| rs2496672260 | 11:118,769,770 | A/G | — | uncertain significance |
| rs2496672517 | 11:118,769,792 | G/C | — | uncertain significance |
| rs765736563 | 11:118,769,802 | C/A | — | uncertain significance |
| rs2496672852 | 11:118,769,819 | G/T | — | uncertain significance |
| rs542302053 | 11:118,769,820 | G/T | — | uncertain significance |
| rs746120292 | 11:118,769,857 | G/A | — | uncertain significance |
| rs2496673380 | 11:118,769,878 | G/A | — | uncertain significance |
| rs1233890904 | 11:118,769,888 | C/G | — | uncertain significance |
| rs2496675011 | 11:118,770,007 | G/A | — | uncertain significance |
| rs754119733 | 11:118,770,079 | C/A | — | uncertain significance |
| rs771732549 | 11:118,770,143 | G/A | — | uncertain significance |
| rs1948200569 | 11:118,770,152 | T/C | — | uncertain significance |
| rs576679220 | 11:118,770,173 | C/T | — | uncertain significance |
| rs1162069113 | 11:118,770,212 | T/C | — | uncertain significance |
| rs200598369 | 11:118,770,632 | C/T | — | uncertain significance |
| rs139987150 | 11:118,770,652 | G/T | — | uncertain significance |
| rs374720039 | 11:118,770,654 | G/T | — | likely benign |
| rs928084930 | 11:118,770,658 | G/T | — | uncertain significance |
| rs776808926 | 11:118,770,860 | C/T | — | uncertain significance |
| rs1476311783 | 11:118,770,866 | G/A | — | uncertain significance |
| rs150970649 | 11:118,770,871 | G/A | — | uncertain significance |
| rs2496686197 | 11:118,771,340 | T/A | — | uncertain significance |
| rs1565614419 | 11:118,771,366 | T/G | — | uncertain significance |
| rs201072117 | 11:118,771,414 | G/A | — | uncertain significance |
| rs749356565 | 11:118,771,427 | C/A | — | uncertain significance |
| rs369209465 | 11:118,771,442 | A/T | — | uncertain significance |
| rs535487538 | 11:118,771,496 | G/A | — | uncertain significance |
| rs775991276 | 11:118,771,546 | G/A | — | uncertain significance |
| rs376130614 | 11:118,771,574 | G/T | — | uncertain significance |
| rs769881421 | 11:118,771,628 | A/T | — | uncertain significance |
| rs377431418 | 11:118,771,672 | G/A | — | uncertain significance |
| rs746679037 | 11:118,771,708 | G/A | — | uncertain significance |
| rs759900233 | 11:118,771,741 | G/A | — | uncertain significance |
| rs34123504 | 11:118,771,747 | A/G | — | benign |
| rs146274685 | 11:118,771,802 | T/C | — | uncertain significance |
| rs762855953 | 11:118,771,821 | C/T | — | uncertain significance |
| rs778060405 | 11:118,771,865 | T/C | — | uncertain significance |
| rs775683494 | 11:118,771,891 | C/T | — | uncertain significance |
| rs1591978624 | 11:118,771,894 | T/C | — | uncertain significance |
| rs547349167 | 11:118,771,990 | C/T | — | uncertain significance |
| rs1212248086 | 11:118,771,994 | C/A | — | uncertain significance |
| rs148630206 | 11:118,772,018 | G/A | — | benign |
| rs149374315 | 11:118,772,082 | C/T | — | benign |
| rs61730467 | 11:118,772,160 | A/G | — | benign |
| rs148554205 | 11:118,772,162 | G/A | — | uncertain significance |
| rs140543345 | 11:118,772,167 | T/C | — | uncertain significance |
| rs1940233272 | 11:118,772,195 | T/C | — | uncertain significance |
| rs768467401 | 11:118,772,198 | G/A | — | uncertain significance |
| rs773017318 | 11:118,772,215 | C/T | — | uncertain significance |
| rs777795040 | 11:118,772,263 | C/T | — | uncertain significance |
| rs1400894466 | 11:118,772,303 | G/C | — | uncertain significance |
| rs369480203 | 11:118,772,311 | G/A | — | uncertain significance |
| rs563843924 | 11:118,772,328 | C/T | — | uncertain significance |
| rs1316029940 | 11:118,772,333 | C/T | — | uncertain significance |
| rs775814948 | 11:118,772,392 | C/T | — | uncertain significance |
| rs751415971 | 11:118,772,399 | C/G | — | uncertain significance |
| rs529047652 | 11:118,772,420 | G/T | — | uncertain significance |
| rs34752197 | 11:118,772,516 | T/C | — | benign |
| rs2496698096 | 11:118,772,558 | G/T | — | uncertain significance |
| rs965417075 | 11:118,772,588 | T/C | — | uncertain significance |
| rs759800909 | 11:118,772,614 | C/A | — | uncertain significance |
| rs764029579 | 11:118,772,623 | C/T | — | uncertain significance |
| rs749719507 | 11:118,772,674 | C/T | — | uncertain significance |
| rs2496699811 | 11:118,772,750 | G/A | — | uncertain significance |
| rs78780803 | 11:118,772,825 | T/C | — | benign |
| rs766799878 | 11:118,773,049 | G/A | — | uncertain significance |
| rs148999907 | 11:118,773,050 | G/A | — | uncertain significance |
| rs771844809 | 11:118,773,085 | G/A | — | uncertain significance |
| rs367909111 | 11:118,773,087 | G/A | — | likely benign |
| rs760057207 | 11:118,773,110 | G/A | — | uncertain significance |
| rs371704255 | 11:118,773,141 | T/A | — | benign |
| rs772758993 | 11:118,773,167 | G/C | — | uncertain significance |
| rs75656086 | 11:118,773,180 | G/A | — | benign |
| rs200847438 | 11:118,773,355 | G/A | — | uncertain significance |
| rs752527554 | 11:118,773,374 | T/C | — | uncertain significance |
Showing 100 of 126 variants. Use the SNP search for the full list.
Gene information from NCBI Gene. Variant classifications from ClinVar.