TRIM33
tripartite motif containing 33
Summary
The protein encoded by this gene is thought to be a transcriptional corepressor. However, molecules that interact with this protein have not yet been identified. The protein is a member of the tripartite motif family. This motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. Three alternatively spliced transcript variants for this gene have been described, however, the full-length nature of one variant has not been determined. [provided by RefSeq, Jul 2008]
Known Variants41 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1125002 | 1:114,938,175 | C/T | 3 prime UTR variant | — |
| rs2525260902 | 1:114,940,307 | C/T | — | uncertain significance |
| rs2525271558 | 1:114,942,134 | T/C | — | uncertain significance |
| rs2525272095 | 1:114,942,231 | T/C | — | uncertain significance |
| rs2179657 | 1:114,945,394 | G/A | — | benign |
| rs6537825 | 1:114,948,281 | A/T | missense variant | — |
| rs56056367 | 1:114,948,309 | A/G | — | benign |
| rs370897114 | 1:114,948,323 | C/G | — | benign |
| rs772897237 | 1:114,949,601 | G/C | — | uncertain significance |
| rs978602778 | 1:114,949,639 | G/C | — | uncertain significance |
| rs67882944 | 1:114,958,202 | T/G | intron variant | — |
| rs3789619 | 1:114,958,946 | A/C | intron variant | — |
| rs2525403811 | 1:114,964,198 | T/C | — | uncertain significance |
| rs527934686 | 1:114,964,205 | G/C | — | benign |
| rs905184942 | 1:114,964,209 | T/G | — | uncertain significance |
| rs764959268 | 1:114,964,225 | C/T | — | uncertain significance |
| rs55763520 | 1:114,964,232 | G/C | — | benign |
| rs2525404367 | 1:114,964,234 | G/T | — | uncertain significance |
| rs753197271 | 1:114,968,182 | A/C | — | uncertain significance |
| rs2525440681 | 1:114,970,462 | C/T | — | benign |
| rs149354552 | 1:114,970,516 | T/G | — | uncertain significance |
| rs12083584 | 1:114,973,429 | T/C | — | benign |
| rs11577901 | 1:115,000,481 | G/A | regulatory region variant | — |
| rs1349147502 | 1:115,006,914 | C/A | — | uncertain significance |
| rs71664847 | 1:115,019,239 | A/T | intron variant | — |
| rs73007266 | 1:115,021,249 | T/C | intron variant | — |
| rs76701955 | 1:115,032,652 | T/C | upstream gene variant | — |
| rs2525926289 | 1:115,053,195 | C/A | — | uncertain significance |
| rs2525926759 | 1:115,053,219 | T/C | — | uncertain significance |
| rs1653289214 | 1:115,053,286 | C/T | — | benign |
| rs1429095582 | 1:115,053,375 | C/G | — | uncertain significance |
| rs989514484 | 1:115,053,379 | G/A | — | uncertain significance |
| rs1205230711 | 1:115,053,381 | G/C | — | uncertain significance |
| rs1423290278 | 1:115,053,399 | G/A | — | uncertain significance |
| rs767671612 | 1:115,053,459 | G/A | — | uncertain significance |
| rs1391339726 | 1:115,053,462 | G/A | — | benign |
| rs554959891 | 1:115,053,465 | G/A | — | uncertain significance |
| rs777482424 | 1:115,053,486 | G/A | — | uncertain significance |
| rs1381254367 | 1:115,053,510 | T/G | — | uncertain significance |
| rs1653314733 | 1:115,053,529 | C/T | — | uncertain significance |
| rs1185411633 | 1:115,053,547 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.