| Gene Symbol | TRIP11 |
| Entrez Gene ID | 9321 |
| Full Name | thyroid hormone receptor interactor 11 |
| Synonyms | ACG1A,CEV14,GMAP-210,GMAP210,TRIP-11,TRIP230 |
| General protein information |
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| Gene Type | protein-coding |
| Organism | Homo sapiens(human) |
| Genome | |
| Summary | This gene was identified based on the interaction of its protein product with thyroid hormone receptor beta. This protein is associated with the Golgi apparatus. The N-terminal region of the protein binds Golgi membranes and the C-terminal region binds the minus ends of microtubules; thus, the protein is thought to play a role in assembly and maintenance of the Golgi ribbon structure around the centrosome. Mutations in this gene cause achondrogenesis type IA.[provided by RefSeq, Mar 2010]. |
| Disorder MIM: | |
| Disorder Html: | Achondrogenesis, type IA, 200600 (3) |
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