TRIM26
tripartite motif containing 26
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. Although the function of the protein is unknown, the RING domain suggests that the protein may have DNA-binding activity. The gene localizes to the major histocompatibility complex (MHC) class I region on chromosome 6. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jun 2011]
Known Variants38 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2517623 | 6:30,152,961 | T/C | downstream gene variant | — |
| rs1446366794 | 6:30,153,813 | C/T | — | uncertain significance |
| rs750752684 | 6:30,153,883 | G/A | — | uncertain significance |
| rs1447809020 | 6:30,153,997 | C/G | — | uncertain significance |
| rs2481603777 | 6:30,154,024 | C/T | — | uncertain significance |
| rs139962336 | 6:30,154,065 | T/A | — | uncertain significance |
| rs761048117 | 6:30,154,101 | T/G | — | uncertain significance |
| rs760252925 | 6:30,154,237 | G/C | — | uncertain significance |
| rs2517622 | 6:30,155,149 | G/A | coding sequence variant | — |
| rs2481734841 | 6:30,156,947 | T/A | — | uncertain significance |
| rs747865368 | 6:30,157,808 | G/A | — | uncertain significance |
| rs9261550 | 6:30,160,906 | T/C | — | — |
| rs2517615 | 6:30,162,505 | G/A | intron variant | — |
| rs141928617 | 6:30,164,357 | C/T | — | uncertain significance |
| rs370328471 | 6:30,164,373 | C/T | — | likely benign |
| rs149492198 | 6:30,164,405 | G/A | — | uncertain significance |
| rs769840905 | 6:30,164,495 | A/G | — | uncertain significance |
| rs367765842 | 6:30,164,496 | T/C | — | likely benign |
| rs2523722 | 6:30,165,273 | C/T | intron variant | — |
| rs533026241 | 6:30,165,837 | G/T | — | — |
| rs752818823 | 6:30,166,211 | C/T | — | uncertain significance |
| rs150992843 | 6:30,166,499 | G/A | — | uncertain significance |
| rs1199750138 | 6:30,166,501 | G/C | — | uncertain significance |
| rs2127510880 | 6:30,166,507 | C/T | — | uncertain significance |
| rs569951003 | 6:30,166,517 | C/T | — | uncertain significance |
| rs147040908 | 6:30,166,601 | G/A | — | uncertain significance |
| rs149959005 | 6:30,166,615 | G/A | — | likely benign |
| rs1395603602 | 6:30,166,732 | C/T | — | uncertain significance |
| rs761026180 | 6:30,166,747 | G/C | — | uncertain significance |
| rs141679609 | 6:30,166,754 | C/T | — | likely benign |
| rs2523720 | 6:30,166,886 | C/T | 5 prime UTR variant | — |
| rs2428503 | 6:30,167,835 | C/T | intron variant | — |
| rs2523716 | 6:30,170,525 | C/T | intron variant | — |
| rs117565607 | 6:30,172,371 | T/A | intron variant | — |
| rs2523712 | 6:30,173,538 | G/A | intron variant | — |
| rs2021722 | 6:30,174,131 | C/T | regulatory region variant | — |
| rs3129695 | 6:30,177,939 | G/A | regulatory region variant | — |
| rs2844775 | 6:30,179,422 | G/A | intron variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.