TRIP11
close
Please copy/paste those URLs into your code to get same results in machine-readable formats:
|
Homo sapiens |
|
TRIP11 is differentially expressed in 289 experiments: 152 organism parts: skin, bone marrow, ... (150 more);, 204 disease states: normal, breast carcinoma, ... (202 more);, 76 cell types 391 cell lines 35 compound treatments and 78 other conditions. |
| Synonyms |
Trip230, CEV14, GMAP-210 |
| Orthologs |
MLP2
(Saccharomyces cerevisiae)
MLP1
(Saccharomyces cerevisiae)
TRIP11
(Gallus gallus)
Trip11
(Mus musculus)
trip11
(Danio rerio)
TRIP11
(Bos taurus)
Tig
(Drosophila melanogaster)
Trip11
(Rattus norvegicus)
NP_001006807.1
(Xenopus laevis)
trip11
(Xenopus laevis)
TRIP11
(Canis familiaris)
(Compare orthologs)
|
| Gene Ontology ID |
GO:0016020, GO:0003713, GO:0000042, GO:0005515, GO:0005737, GO:0005634, GO:0005856, GO:0005794, GO:0006366, GO:0043231 |
| InterPro ID |
IPR000237 |
| Gene Ontology Term |
protein binding, protein targeting to Golgi, cytoskeleton, cytoplasm, membrane, Golgi apparatus, transcription from RNA polymerase II promoter, intracellular membrane-bounded organelle, transcription coactivator activity, nucleus |
| InterPro Term |
GRIP |
| Ensembl Family Description |
THYROID RECEPTOR INTERACTING 11 TR INTERACTING 11 TRIP 11 CLONAL EVOLUTION RELATED GENE ON CHROMOSOME 14 GOLGI ASSOCIATED MICROTUBULE BINDING 210 GMAP 210 TRIP230 |
| Ensembl Family |
ENSFM00250000003391 |
| EMBL-Bank ID |
L40380, Y12490, AF011368, AL049872, AF007217 |
| Ensembl Protein ID |
ENSP00000267622, ENSP00000445676, ENSP00000451032, ENSP00000451607, ENSP00000451944 |
| UniProt Accession |
Q15643, F5H1Z0 |
| Entrez Gene ID |
9321 |
| Ensembl Gene ID |
ENSG00000100815 |
| UniGene ID |
Hs.632339, Hs.713299, Hs.627136, Hs.600848, Hs.712145, Hs.591417 |
| RefSeq ID |
NM_004239, NP_004230 |
| Description |
thyroid hormone receptor interactor 11 [Source:HGNC Symbol;Acc:12305] |
| HGNC Symbol |
TRIP11 |
| Ensembl Transcript ID |
ENST00000554357, ENST00000267622, ENST00000542257, ENST00000555105, ENST00000555516, ENST00000557017 |
| Gene-Disease Assocation |
ACHONDROGENESIS, TYPE IA; ACG1A |
| Design Element |
L40380_at, ENST00000555105, ENST00000267622, ENST00000557017, 209778_at, 81684_at, g2253416_3p_at, 236160_at, 55474_at, Hs.95097.0.A1_3p_at, ENST00000555516, g12803642_3p_x_at, 210760_x_at, 37932_at, 210760_3p_x_at, 82204_at, ENST00000542257, 230211_at, Hs.122826.0.A1_3p_at, ENST00000554357 |
| Search EB-eye |
ENSG00000100815
|
 Show more
properties
|
|
