TRIM27
tripartite motif containing 27
Summary
This gene encodes a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nuclear matrix. It interacts with the enhancer of polycomb protein and represses gene transcription. It is also thought to be involved in the differentiation of male germ cells. Fusion of the N-terminus of this protein with the truncated C-terminus of the RET gene product has been shown to result in production of the ret transforming protein. [provided by RefSeq, Jul 2008]
Known Variants25 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1010599059 | 6:28,871,864 | T/C | — | uncertain significance |
| rs987158622 | 6:28,871,894 | A/G | — | uncertain significance |
| rs141782592 | 6:28,871,904 | T/C | — | uncertain significance |
| rs2546930226 | 6:28,872,187 | G/A | — | uncertain significance |
| rs2546930245 | 6:28,872,202 | C/G | — | uncertain significance |
| rs2546930268 | 6:28,872,220 | T/A | — | uncertain significance |
| rs761287371 | 6:28,872,254 | C/T | — | uncertain significance |
| rs3118363 | 6:28,875,501 | T/C | — | — |
| rs3135293 | 6:28,877,247 | T/C | intron variant | — |
| rs3132382 | 6:28,883,296 | G/A | upstream gene variant | — |
| rs3131101 | 6:28,885,863 | A/G | downstream gene variant | — |
| rs3132378 | 6:28,885,865 | A/G | downstream gene variant | — |
| rs12212813 | 6:28,885,957 | A/T | — | — |
| rs576269250 | 6:28,887,835 | G/A | — | uncertain significance |
| rs139570691 | 6:28,887,889 | T/C | — | uncertain significance |
| rs144996521 | 6:28,889,415 | G/A | intron variant | — |
| rs2546968060 | 6:28,889,712 | T/C | — | uncertain significance |
| rs2546970184 | 6:28,891,052 | G/C | — | uncertain significance |
| rs1774198757 | 6:28,891,106 | G/A | — | uncertain significance |
| rs914036518 | 6:28,891,163 | T/A | — | uncertain significance |
| rs757362963 | 6:28,891,256 | A/G | — | uncertain significance |
| rs61759897 | 6:28,891,348 | T/C | — | uncertain significance |
| rs1774233924 | 6:28,891,375 | T/C | — | uncertain significance |
| rs3131103 | 6:28,893,534 | C/G | upstream gene variant | — |
| rs13206458 | 6:28,893,573 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.