STAU1
staufen double-stranded RNA binding protein 1
Summary
Staufen is a member of the family of double-stranded RNA (dsRNA)-binding proteins involved in the transport and/or localization of mRNAs to different subcellular compartments and/or organelles. These proteins are characterized by the presence of multiple dsRNA-binding domains which are required to bind RNAs having double-stranded secondary structures. The human homologue of staufen encoded by STAU, in addition contains a microtubule- binding domain similar to that of microtubule-associated protein 1B, and binds tubulin. The STAU gene product has been shown to be present in the cytoplasm in association with the rough endoplasmic reticulum (RER), implicating this protein in the transport of mRNA via the microtubule network to the RER, the site of translation. [provided by RefSeq, Apr 2020]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs948177814 | 20:47,732,400 | G/A | — | uncertain significance |
| rs767899710 | 20:47,734,375 | T/C | — | uncertain significance |
| rs570607143 | 20:47,734,412 | T/C | — | uncertain significance |
| rs150236575 | 20:47,734,463 | T/A | — | uncertain significance |
| rs767562430 | 20:47,734,477 | G/T | — | uncertain significance |
| rs2515576752 | 20:47,734,507 | A/G | — | uncertain significance |
| rs779218078 | 20:47,736,562 | G/A | — | uncertain significance |
| rs138430183 | 20:47,736,604 | T/G | — | uncertain significance |
| rs771766932 | 20:47,739,660 | C/G | — | uncertain significance |
| rs751744032 | 20:47,739,763 | T/G | — | uncertain significance |
| rs2092546969 | 20:47,741,077 | C/G | — | uncertain significance |
| rs6063357 | 20:47,743,110 | G/A | — | — |
| rs776310026 | 20:47,752,434 | T/C | — | uncertain significance |
| rs61418814 | 20:47,769,838 | C/T | — | — |
| rs2273652 | 20:47,770,461 | C/A | — | benign |
| rs754717987 | 20:47,770,477 | G/A | — | uncertain significance |
| rs748741131 | 20:47,770,512 | G/T | — | uncertain significance |
| rs146302958 | 20:47,770,518 | A/G | — | uncertain significance |
| rs17450430 | 20:47,772,264 | A/G | — | — |
| rs6019663 | 20:47,774,512 | T/G | — | — |
| rs2426139 | 20:47,780,105 | G/A | intron variant | — |
| rs769641260 | 20:47,782,624 | T/C | — | likely benign |
| rs189127126 | 20:47,782,687 | T/G | — | uncertain significance |
| rs13039749 | 20:47,800,615 | C/T | intron variant | — |
| rs13041213 | 20:47,800,829 | T/A | intron variant | — |
| rs35667796 | 20:47,803,301 | A/C | regulatory region variant | — |
| rs3795075 | 20:47,806,092 | G/A | upstream gene variant | — |
| rs6019670 | 20:47,810,699 | C/G | — | — |
| rs74744146 | 20:47,813,321 | G/A | — | — |
| rs78387210 | 20:47,823,441 | C/A | — | — |
| rs73611371 | 20:47,835,155 | T/A | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.