TRIM6-TRIM34 (TRIM6-TRIM34 readthrough)
|
Gene
Gene information from NCBI Gene database.
|
|
| Entrez ID | 445372 |
| Gene name | TRIM6-TRIM34 readthrough |
| Gene symbol | TRIM6-TRIM34 |
| Synonyms (NCBI Gene) |
IFP1RNF21RNF89TRIM34TRIM6
|
| Chromosome | 11 |
| Chromosome location | 11p15.4 |
| 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. This gene represents a readthrough transcript from |
|
miRNA
miRNA information provided by mirtarbase database.
55
|
|||||||||||||||||||||||||
|
|||||||||||||||||||||||||
|
Other IDs
Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
|
|||||||
|
|||||||
|
Associated diseases
Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
|
|||||||||||||||||
|
Evidence Score:
★☆☆☆☆ Gene-disease association found in Text Mining only
★★☆☆☆ Found in Text Mining and Unknown/Other Associations
★★★☆☆ Reported in Unknown/Other Associations across ≥2 Sources
★★★★☆ ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
★★★★★ ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
|
|||||||||||||||||
|
|||||||||||||||||