FBXO41
F-box protein 41
Summary
This gene encodes a member of the F-box protein family, which is characterized by an approximately 40 amino acid motif, the F-box. F-box proteins constitute one of the four subunits of the SCF ubiquitin protein ligase complex that plays a role in phosphorylation-dependent ubiquitination. F-box proteins are divided into three classes depending on the interaction substrate domain each contains in addition to the F-box motif: FBXW proteins contain WD-40 domains, FBXL proteins contain leucine-rich repeats, and FBXO proteins contain either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene belongs to the FBXO class. [provided by RefSeq, Feb 2014]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs199625082 | 2:73,486,118 | C/T | — | uncertain significance |
| rs765528062 | 2:73,486,153 | C/G | — | uncertain significance |
| rs200703280 | 2:73,487,547 | C/T | — | uncertain significance |
| rs2529889289 | 2:73,487,549 | G/A | — | uncertain significance |
| rs2529889648 | 2:73,487,585 | A/G | — | uncertain significance |
| rs372612044 | 2:73,487,594 | C/A | — | uncertain significance |
| rs1687973863 | 2:73,487,660 | C/T | — | uncertain significance |
| rs765916084 | 2:73,487,960 | C/T | — | uncertain significance |
| rs755363542 | 2:73,487,961 | G/A | — | uncertain significance |
| rs1239912088 | 2:73,487,973 | G/T | — | uncertain significance |
| rs1169821595 | 2:73,490,864 | C/T | — | uncertain significance |
| rs367605676 | 2:73,490,909 | T/A | — | uncertain significance |
| rs371994505 | 2:73,491,438 | C/A | — | uncertain significance |
| rs572663604 | 2:73,491,473 | C/T | — | uncertain significance |
| rs762826333 | 2:73,491,474 | G/A | — | uncertain significance |
| rs891391428 | 2:73,491,531 | A/G | — | uncertain significance |
| rs2529907740 | 2:73,491,557 | T/C | — | uncertain significance |
| rs748513064 | 2:73,491,590 | C/T | — | uncertain significance |
| rs753891746 | 2:73,491,591 | G/A | — | uncertain significance |
| rs749845167 | 2:73,491,617 | C/T | — | uncertain significance |
| rs200040373 | 2:73,491,623 | C/T | — | uncertain significance |
| rs371450076 | 2:73,492,401 | G/A | — | benign |
| rs534854964 | 2:73,492,457 | C/T | — | uncertain significance |
| rs199920424 | 2:73,492,458 | G/A | — | uncertain significance |
| rs2529912541 | 2:73,492,467 | C/A | — | uncertain significance |
| rs755079022 | 2:73,492,508 | A/G | — | uncertain significance |
| rs748830200 | 2:73,492,530 | C/T | — | uncertain significance |
| rs202215539 | 2:73,492,551 | G/A | — | uncertain significance |
| rs370031029 | 2:73,492,560 | G/A | — | uncertain significance |
| rs199960192 | 2:73,492,584 | G/A | — | uncertain significance |
| rs200871330 | 2:73,492,586 | C/T | — | uncertain significance |
| rs374143533 | 2:73,492,587 | G/A | — | uncertain significance |
| rs2529914175 | 2:73,492,670 | C/T | — | uncertain significance |
| rs760493770 | 2:73,492,746 | C/T | — | uncertain significance |
| rs764967523 | 2:73,492,763 | G/C | — | uncertain significance |
| rs2529916454 | 2:73,493,024 | G/A | — | uncertain significance |
| rs374564267 | 2:73,493,075 | G/A | — | uncertain significance |
| rs200330670 | 2:73,493,602 | G/A | — | uncertain significance |
| rs2529920431 | 2:73,493,607 | T/C | — | uncertain significance |
| rs562151414 | 2:73,493,613 | C/T | — | uncertain significance |
| rs1688283530 | 2:73,493,664 | C/T | — | uncertain significance |
| rs201580699 | 2:73,493,745 | C/T | — | uncertain significance |
| rs2529921636 | 2:73,493,757 | C/T | — | uncertain significance |
| rs373376404 | 2:73,493,775 | G/A | — | uncertain significance |
| rs775918372 | 2:73,493,794 | C/T | — | uncertain significance |
| rs1295004951 | 2:73,496,116 | C/T | — | uncertain significance |
| rs1219119646 | 2:73,496,292 | T/C | — | uncertain significance |
| rs1159910979 | 2:73,496,404 | G/A | — | uncertain significance |
| rs929634537 | 2:73,496,424 | T/C | — | uncertain significance |
| rs1366354002 | 2:73,496,466 | G/A | — | uncertain significance |
| rs907100179 | 2:73,496,554 | C/T | — | uncertain significance |
| rs1034121398 | 2:73,496,565 | G/A | — | uncertain significance |
| rs149852572 | 2:73,505,422 | A/G | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.