RSF1
remodeling and spacing factor 1
Summary
This gene encodes a nuclear protein that interacts with hepatitis B virus X protein (HBX) and facilitates transcription of hepatitis B virus genes by the HBX transcription activator, suggesting a role for this interaction in the virus life cycle. This protein also interacts with SNF2H protein to form the RSF chromatin-remodeling complex, where the SNF2H subunit functions as the nucleosome-dependent ATPase, and this protein as the histone chaperone. [provided by RefSeq, Sep 2011]
Known Variants64 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs752047906 | 11:77,378,045 | C/T | — | uncertain significance |
| rs2542661063 | 11:77,378,098 | T/C | — | uncertain significance |
| rs1481787845 | 11:77,378,164 | C/T | — | uncertain significance |
| rs769419586 | 11:77,378,275 | T/C | — | uncertain significance |
| rs375656054 | 11:77,378,384 | G/A | — | uncertain significance |
| rs781247505 | 11:77,378,398 | C/T | — | uncertain significance |
| rs777265824 | 11:77,378,414 | C/T | — | uncertain significance |
| rs369345479 | 11:77,378,435 | C/T | — | uncertain significance |
| rs201625012 | 11:77,378,446 | T/C | — | uncertain significance |
| rs11607608 | 11:77,378,448 | C/T | — | likely benign |
| rs374984667 | 11:77,378,482 | C/T | — | likely benign |
| rs199889950 | 11:77,378,483 | G/A | — | uncertain significance |
| rs148454072 | 11:77,383,137 | T/G | — | uncertain significance |
| rs369187639 | 11:77,383,166 | G/A | — | likely benign |
| rs139872567 | 11:77,383,248 | T/C | — | uncertain significance |
| rs2542683973 | 11:77,386,114 | C/T | — | uncertain significance |
| rs151055861 | 11:77,386,294 | C/T | — | uncertain significance |
| rs1329254480 | 11:77,387,877 | C/A | — | uncertain significance |
| rs1959722361 | 11:77,387,990 | A/G | — | uncertain significance |
| rs2135842828 | 11:77,404,583 | T/C | — | uncertain significance |
| rs758032406 | 11:77,409,656 | C/T | — | uncertain significance |
| rs984929930 | 11:77,409,660 | C/G | — | uncertain significance |
| rs368439164 | 11:77,411,837 | C/T | — | uncertain significance |
| rs2542753658 | 11:77,411,843 | A/G | — | uncertain significance |
| rs150024260 | 11:77,411,845 | T/A | — | uncertain significance |
| rs775845254 | 11:77,411,979 | T/G | — | uncertain significance |
| rs753497749 | 11:77,412,025 | G/T | — | uncertain significance |
| rs781442025 | 11:77,412,037 | G/A | — | uncertain significance |
| rs773192528 | 11:77,412,172 | A/G | — | uncertain significance |
| rs774971554 | 11:77,412,182 | T/C | — | uncertain significance |
| rs141788361 | 11:77,412,194 | G/A | — | uncertain significance |
| rs1960412548 | 11:77,412,224 | C/G | — | uncertain significance |
| rs199916779 | 11:77,412,230 | T/C | — | uncertain significance |
| rs780968337 | 11:77,412,281 | C/T | — | uncertain significance |
| rs1960414165 | 11:77,412,284 | C/G | — | uncertain significance |
| rs367966600 | 11:77,412,302 | C/G | — | uncertain significance |
| rs777566054 | 11:77,412,376 | T/C | — | uncertain significance |
| rs745775941 | 11:77,412,431 | G/C | — | uncertain significance |
| rs748974803 | 11:77,412,434 | T/C | — | uncertain significance |
| rs138660432 | 11:77,412,455 | G/C | — | uncertain significance |
| rs1430392536 | 11:77,412,538 | G/A | — | uncertain significance |
| rs770333020 | 11:77,412,577 | C/A | — | likely benign |
| rs1409540945 | 11:77,412,587 | T/A | — | uncertain significance |
| rs369759711 | 11:77,412,596 | C/T | — | uncertain significance |
| rs2542757361 | 11:77,412,632 | T/C | — | uncertain significance |
| rs371922152 | 11:77,412,829 | G/A | — | likely benign |
| rs754245168 | 11:77,412,874 | G/T | — | uncertain significance |
| rs758413705 | 11:77,412,894 | T/C | — | likely benign |
| rs776249119 | 11:77,413,070 | G/A | — | uncertain significance |
| rs1351725579 | 11:77,413,073 | C/T | — | uncertain significance |
| rs1332409005 | 11:77,413,321 | T/C | — | uncertain significance |
| rs12418559 | 11:77,425,988 | A/C | downstream gene variant | — |
| rs145721717 | 11:77,427,863 | C/G | downstream gene variant | — |
| rs773402875 | 11:77,436,650 | G/A | — | uncertain significance |
| rs112929118 | 11:77,447,335 | T/G | — | — |
| rs141688686 | 11:77,451,894 | T/C | — | uncertain significance |
| rs764673941 | 11:77,458,107 | C/T | — | uncertain significance |
| rs553269512 | 11:77,463,878 | A/G | — | — |
| rs567783044 | 11:77,485,541 | C/T | — | — |
| rs755222980 | 11:77,488,865 | A/C | — | — |
| rs570786 | 11:77,507,332 | G/A | — | — |
| rs4469913 | 11:77,517,812 | C/T | — | — |
| rs618535 | 11:77,525,203 | G/A | upstream gene variant | — |
| rs2542999131 | 11:77,531,700 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.