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Gene : TRIP11 Homo sapiens

Name  ? thyroid hormone receptor interactor 11 Cytological Location  14q32.12
Brief Description  thyroid hormone receptor interactor 11
Description  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]
  • synonyms:
  • GMAP210,
  • ACG1A,
  • OTTHUMG00000171128,
  • CEV14,
  • ODCD,
  • GMAP-210,
  • TRIP230,
  • uc001xzy.4,
  • GMAP-210,
  • HGNC:12305,
  • golgi-microtubule-associated-protein of 210 kDa,
  • NM_001321851,
  • TRIP11,
  • CEV14,
  • Trip230,
  • L40380,
  • TRIP-11,
  • GMAP210
  • identifiers:
  • 9321,
  • ENSG00000100815,
  • TRIP11

Genome feature

Region: gene ? Length: 74144  
Location: 14:91965991-92040134 reverse strand Cyto location: 14q32.12


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Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

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SNPs

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Disease

2 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

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Other

3756 SN Ps

5 Cross References

19 Data Sets

6 Homologues

0 Located Features

97 Rna Seq Results