WBP1L
WW domain binding protein 1 like
Summary
Predicted to enable ubiquitin protein ligase binding activity. Predicted to be involved in CXCL12-activated CXCR4 signaling pathway. Predicted to act upstream of or within hemopoiesis and positive regulation of protein ubiquitination. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1170755396 | 10:104,503,892 | C/T | — | uncertain significance |
| rs11191385 | 10:104,513,049 | G/T | regulatory region variant | — |
| rs4919670 | 10:104,515,799 | C/A | intron variant | — |
| rs11191392 | 10:104,526,951 | C/T | — | — |
| rs61870777 | 10:104,531,148 | T/G | intron variant | — |
| rs2253709 | 10:104,542,745 | T/A | regulatory region variant | — |
| rs75731980 | 10:104,548,027 | C/T | intron variant | — |
| rs2250301 | 10:104,548,393 | G/A | intron variant | — |
| rs176185 | 10:104,556,054 | G/C | intron variant | — |
| rs2482508 | 10:104,558,961 | C/T | upstream gene variant | — |
| rs139247810 | 10:104,561,078 | T/G | regulatory region variant | — |
| rs141913574 | 10:104,566,988 | G/A | — | — |
| rs182071475 | 10:104,567,876 | C/T | downstream gene variant | — |
| rs1000447498 | 10:104,569,743 | G/A | — | uncertain significance |
| rs146918058 | 10:104,569,773 | G/A | — | uncertain significance |
| rs78479341 | 10:104,569,794 | C/T | — | uncertain significance |
| rs528315445 | 10:104,572,490 | C/G | — | uncertain significance |
| rs373251237 | 10:104,572,505 | C/T | — | uncertain significance |
| rs762607950 | 10:104,572,544 | C/T | — | uncertain significance |
| rs751075397 | 10:104,572,570 | C/T | — | uncertain significance |
| rs568846569 | 10:104,572,652 | G/A | — | uncertain significance |
| rs139434993 | 10:104,572,759 | G/A | — | uncertain significance |
| rs758636598 | 10:104,572,834 | C/T | — | uncertain significance |
| rs750852779 | 10:104,572,862 | A/G | — | uncertain significance |
| rs201482384 | 10:104,572,927 | C/T | — | uncertain significance |
| rs367613441 | 10:104,572,943 | A/C | — | uncertain significance |
| rs142388099 | 10:104,572,958 | G/A | — | uncertain significance |
| rs761880948 | 10:104,572,997 | C/T | — | uncertain significance |
| rs284856 | 10:104,574,329 | A/T | regulatory region variant | — |
| rs6892 | 10:104,575,870 | A/G | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.