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Details of TRIM33 gene in Homo sapiens
IDs |
|---|
| Link outs |
Gene Name |
Alias |
Uniprot ID |
SwissProt ID |
NCBI gene ID |
ENSEMBL ID |
Description |
Source |
|
| TRIM33 | KIAA1113,RFG7,TIF1G | Q9UPN9 | TRI33_HUMAN | 51592
| ENSG00000197323
| E3 ubiquitin-protein ligase TRIM33 | SPROT |
Disease |
|---|
| Disease |
OMIM id |
| Thyroid papillary carcinoma (TPC) [MIM:188550]: A common tumor of the thyroid that typically arises as an irregular, solid or cystic mass from otherwise normal thyroid tissue. Papillary carcinomas are malignant neoplasm characterized by the formation of numerous, irregular, finger-like projections of fibrous stroma that is covered with a surface layer of neoplastic epithelial cells. Note=The disease is caused by mutations affecting the gene represented in this entry. A chromosomal aberration involving TRIM33 is found in thyroid papillary carcinomas. Translocation t(110)(p13q11) with RET. The translocation generates the TRIM33/RET (PTC7) oncogene. |
188550 |
Orthologs in other species |
|---|
| M. musculus |
D. melonogaster |
C. elegans |
S. purpuratus |
| Trim33 | bon | --- | Sp-Ectdrn |
