RBM23
RNA binding motif protein 23
Summary
This gene encodes a member of the U2AF-like family of RNA binding proteins. This protein interacts with some steroid nuclear receptors, localizes to the promoter of a steroid- responsive gene, and increases transcription of steroid-responsive transcriptional reporters in a hormone-dependent manner. It is also implicated in the steroid receptor-dependent regulation of alternative splicing. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Known Variants44 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs756624982 | 14:23,371,042 | G/A | — | uncertain significance |
| rs2501936400 | 14:23,371,080 | G/A | — | uncertain significance |
| rs200611630 | 14:23,371,215 | C/T | — | uncertain significance |
| rs746926514 | 14:23,371,485 | C/A | — | uncertain significance |
| rs547621969 | 14:23,371,518 | C/G | — | uncertain significance |
| rs372726982 | 14:23,371,547 | A/C | — | uncertain significance |
| rs201562748 | 14:23,371,567 | G/A | — | uncertain significance |
| rs12437151 | 14:23,372,913 | G/C | — | — |
| rs557116761 | 14:23,373,495 | C/T | — | uncertain significance |
| rs368166923 | 14:23,373,496 | G/A | — | uncertain significance |
| rs781160232 | 14:23,373,501 | G/A | — | uncertain significance |
| rs947929194 | 14:23,374,085 | T/C | — | uncertain significance |
| rs375240077 | 14:23,374,172 | T/C | — | likely benign |
| rs2502022300 | 14:23,374,193 | G/C | — | uncertain significance |
| rs543364121 | 14:23,374,196 | A/T | — | uncertain significance |
| rs1566545574 | 14:23,374,368 | G/C | — | uncertain significance |
| rs984413641 | 14:23,374,440 | T/C | — | uncertain significance |
| rs187229917 | 14:23,374,449 | C/T | — | uncertain significance |
| rs368778639 | 14:23,374,579 | C/T | — | uncertain significance |
| rs373466451 | 14:23,374,585 | C/T | — | uncertain significance |
| rs1166395114 | 14:23,374,625 | C/A | — | uncertain significance |
| rs779737231 | 14:23,374,630 | C/T | — | uncertain significance |
| rs761437876 | 14:23,375,447 | G/A | — | uncertain significance |
| rs750729529 | 14:23,375,450 | G/A | — | uncertain significance |
| rs200231890 | 14:23,375,464 | C/T | — | uncertain significance |
| rs775566402 | 14:23,375,479 | T/G | — | uncertain significance |
| rs201485980 | 14:23,375,482 | C/T | — | uncertain significance |
| rs371577602 | 14:23,375,492 | A/G | — | uncertain significance |
| rs369065745 | 14:23,375,503 | C/T | — | uncertain significance |
| rs372628717 | 14:23,375,504 | G/A | — | uncertain significance |
| rs774538213 | 14:23,375,557 | C/T | — | uncertain significance |
| rs760125299 | 14:23,375,558 | G/A | — | uncertain significance |
| rs1168156871 | 14:23,377,546 | G/A | — | uncertain significance |
| rs548036119 | 14:23,377,557 | C/A | — | uncertain significance |
| rs778545926 | 14:23,378,731 | T/C | — | likely benign |
| rs200447116 | 14:23,378,803 | T/A | — | uncertain significance |
| rs376713891 | 14:23,380,539 | C/G | — | uncertain significance |
| rs1215450017 | 14:23,380,572 | C/T | — | uncertain significance |
| rs4981446 | 14:23,381,413 | A/G | intron variant | — |
| rs10137343 | 14:23,382,640 | A/C | — | — |
| rs189275070 | 14:23,384,832 | G/A | downstream gene variant | — |
| rs561256539 | 14:23,386,412 | G/C | — | — |
| rs34344888 | 14:23,387,585 | A/G | downstream gene variant | — |
| rs55898715 | 14:23,387,609 | T/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.