SNX33
sorting nexin 33
Summary
The protein encoded by this gene is involved in cytoskeletal reorganization, vesicle trafficking, endocytosis, and mitosis. The encoded protein is essential for the creation of the cleavage furrow during mitosis and for completion of mitosis. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Dec 2015]
Known Variants31 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs866932557 | 15:75,941,460 | G/A | — | uncertain significance |
| rs140797653 | 15:75,941,476 | T/C | — | likely benign |
| rs367776246 | 15:75,941,618 | G/A | — | likely benign |
| rs2505046745 | 15:75,941,682 | C/T | — | uncertain significance |
| rs779203982 | 15:75,941,742 | G/A | — | uncertain significance |
| rs1167906480 | 15:75,941,762 | G/C | — | uncertain significance |
| rs371112191 | 15:75,941,779 | T/G | — | uncertain significance |
| rs376433115 | 15:75,941,787 | A/G | — | uncertain significance |
| rs151223588 | 15:75,941,825 | G/A | — | uncertain significance |
| rs779081434 | 15:75,941,834 | C/T | — | uncertain significance |
| rs372555211 | 15:75,941,843 | G/A | — | uncertain significance |
| rs996682669 | 15:75,941,889 | G/C | — | uncertain significance |
| rs757817318 | 15:75,941,918 | C/T | — | uncertain significance |
| rs201668627 | 15:75,941,922 | C/T | — | uncertain significance |
| rs989777038 | 15:75,941,943 | A/G | — | uncertain significance |
| rs372586273 | 15:75,942,067 | C/G | — | uncertain significance |
| rs139083526 | 15:75,942,326 | A/G | — | uncertain significance |
| rs765623933 | 15:75,942,449 | C/G | — | uncertain significance |
| rs1893558915 | 15:75,942,506 | G/A | — | uncertain significance |
| rs1429978805 | 15:75,942,590 | G/T | — | uncertain significance |
| rs765854890 | 15:75,942,617 | G/A | — | uncertain significance |
| rs745967075 | 15:75,942,674 | C/T | — | uncertain significance |
| rs2505049023 | 15:75,942,776 | C/T | — | uncertain significance |
| rs757462528 | 15:75,942,780 | C/T | — | uncertain significance |
| rs746150677 | 15:75,942,785 | C/T | — | uncertain significance |
| rs139396216 | 15:75,942,786 | G/A | — | uncertain significance |
| rs1893661346 | 15:75,949,381 | G/A | — | uncertain significance |
| rs140532329 | 15:75,949,395 | G/T | — | uncertain significance |
| rs757588322 | 15:75,949,441 | G/A | — | uncertain significance |
| rs747006284 | 15:75,949,482 | C/G | — | uncertain significance |
| rs112473234 | 15:75,953,547 | G/T | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.