| Entrez Gene ID | 445372 |
|---|---|
| Official Gene Symbol | TRIM6-TRIM34 (GeneCards) |
| Full name | TRIM6-TRIM34 readthrough |
| Location | 11p15.4 |
| Other ids | Vega : OTTHUMG00000066899 HGNC : HGNC:33440 Ensembl : ENSG00000258588 |
| Other names | IFP1, RNF21, TRIM34 |
| 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. This gene represents a readthrough transcript from genes TRIM6 and TRIM34, and it was described as a splice variant of TRIM34. This gene is mapped to chromosome 11p15, where it resides within a TRIM gene cluster. [provided by RefSeq, Nov 2009] |
Found 1 variant in this database.
| Variant ID | Entrez Gene ID | Gene | Chromsome | Start | End | Disease | Method |
|---|---|---|---|---|---|---|---|
| 15824 | 445372 | TRIM6-TRIM34 | 11 | 5673117 | 5673117 | Cockayne syndrome | HiSeq X Ten |