TRIM4
tripartite motif containing 4
Summary
The protein encoded by this gene is 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. The protein localizes to cytoplasmic bodies. Its function has not been identified. Alternatively spliced transcript variants that encode different isoforms have been described.[provided by RefSeq, Jul 2010]
Known Variants37 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs17277546 | 7:99,489,571 | G/A | 3 prime UTR variant | — |
| rs2546732338 | 7:99,489,831 | A/C | — | uncertain significance |
| rs773814499 | 7:99,489,875 | A/G | — | uncertain significance |
| rs201814883 | 7:99,489,896 | C/T | — | uncertain significance |
| rs372374118 | 7:99,489,902 | C/T | — | uncertain significance |
| rs1563081970 | 7:99,489,922 | T/G | — | uncertain significance |
| rs544095744 | 7:99,489,935 | G/C | — | uncertain significance |
| rs576660959 | 7:99,490,002 | C/A | — | uncertain significance |
| rs750116992 | 7:99,490,070 | G/A | — | uncertain significance |
| rs201126235 | 7:99,490,139 | C/G | — | uncertain significance |
| rs777100871 | 7:99,490,205 | T/C | — | uncertain significance |
| rs763387987 | 7:99,490,238 | A/G | — | uncertain significance |
| rs149678278 | 7:99,490,298 | T/C | — | uncertain significance |
| rs267601667 | 7:99,490,337 | G/A | — | uncertain significance |
| rs764872137 | 7:99,500,849 | C/T | — | likely benign |
| rs2546737899 | 7:99,500,878 | C/G | — | uncertain significance |
| rs774210115 | 7:99,501,202 | G/T | — | uncertain significance |
| rs139038907 | 7:99,501,208 | A/T | — | uncertain significance |
| rs1178582366 | 7:99,506,225 | G/C | — | uncertain significance |
| rs147278816 | 7:99,506,401 | G/A | — | uncertain significance |
| rs745931126 | 7:99,506,416 | C/T | — | uncertain significance |
| rs762624048 | 7:99,507,202 | C/T | — | uncertain significance |
| rs768768697 | 7:99,507,277 | G/T | — | uncertain significance |
| rs766007111 | 7:99,514,377 | T/C | missense variant | — |
| rs902484291 | 7:99,516,670 | C/T | — | uncertain significance |
| rs2546746924 | 7:99,516,699 | C/A | — | uncertain significance |
| rs2546746931 | 7:99,516,708 | C/T | — | uncertain significance |
| rs948087578 | 7:99,516,730 | C/T | — | uncertain significance |
| rs751960914 | 7:99,516,778 | G/T | — | uncertain significance |
| rs551507004 | 7:99,516,792 | C/G | — | uncertain significance |
| rs1018879961 | 7:99,516,816 | A/G | — | uncertain significance |
| rs777662129 | 7:99,516,828 | G/A | — | uncertain significance |
| rs2546747284 | 7:99,516,861 | G/A | — | uncertain significance |
| rs575184410 | 7:99,516,908 | G/C | — | uncertain significance |
| rs545753250 | 7:99,516,940 | G/C | — | uncertain significance |
| rs2546747471 | 7:99,516,965 | C/G | — | uncertain significance |
| rs770148766 | 7:99,516,997 | A/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.