MSI2
musashi RNA binding protein 2
Summary
This gene encodes an RNA-binding protein that is a member of the Musashi protein family. The encoded protein is transcriptional regulator that targets genes involved in development and cell cycle regulation. Mutations in this gene are associated with poor prognosis in certain types of cancers. This gene has also been shown to be rearranged in certain cancer cells. [provided by RefSeq, Apr 2016]
Known Variants30 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs753289768 | 17:55,334,838 | G/A | — | uncertain significance |
| rs4239207 | 17:55,361,179 | G/A | — | — |
| rs13353194 | 17:55,362,972 | G/C | — | — |
| rs792376 | 17:55,438,556 | A/C | — | — |
| rs78310935 | 17:55,449,072 | C/T | intron variant | — |
| rs118121072 | 17:55,463,336 | G/A | intron variant | — |
| rs116853700 | 17:55,466,295 | G/A | intron variant | — |
| rs150497606 | 17:55,466,426 | G/A | intron variant | — |
| rs2544602620 | 17:55,478,812 | T/C | — | uncertain significance |
| rs1281593215 | 17:55,607,056 | T/C | — | uncertain significance |
| rs565719871 | 17:55,628,589 | G/A | — | — |
| rs796256065 | 17:55,653,987 | T/A | — | — |
| rs72833096 | 17:55,655,932 | G/C | regulatory region variant | — |
| rs72833102 | 17:55,663,552 | G/T | — | — |
| rs16958566 | 17:55,664,754 | T/A | intron variant | — |
| rs761315422 | 17:55,674,301 | A/G | — | uncertain significance |
| rs556998079 | 17:55,686,640 | G/A | — | — |
| rs749045445 | 17:55,693,385 | G/A | — | uncertain significance |
| rs35065479 | 17:55,736,735 | G/C | — | — |
| rs4793888 | 17:55,737,740 | G/A | intron variant | — |
| rs11079321 | 17:55,747,416 | G/C | — | — |
| rs778502926 | 17:55,752,353 | G/A | — | uncertain significance |
| rs1221930442 | 17:55,752,401 | G/A | — | uncertain significance |
| rs199615350 | 17:55,752,410 | A/G | — | uncertain significance |
| rs1330705211 | 17:55,752,429 | G/A | — | uncertain significance |
| rs145329279 | 17:55,752,473 | G/A | — | uncertain significance |
| rs759553636 | 17:55,754,360 | G/A | — | uncertain significance |
| rs562720172 | 17:55,766,342 | G/A | — | — |
| rs9891544 | 17:55,771,339 | A/G | intergenic variant | — |
| rs74601275 | 17:55,776,915 | A/G | intergenic variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.