Bos taurus Gene: THRB
Summary
InnateDB Gene IDBG-630420.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol THRB
Gene Name Uncharacterized protein
Synonyms TRbeta1
Species Bos taurus
Ensembl Gene ENSBTAG00000017802
Encoded Proteins
thyroid hormone receptor, beta
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation from Orthologs
Summary
[Homo sapiens] THRB signalling plays a role in modulating dendritic cell (DC) physiology and has immunoregulatory effects. THRB contains an NF-kappaB consensus site in its promoter region that controls its expression, which in turn signals DCs to promote maturation and function via an Akt-dependent, but PI3K independent pathway.
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000151090:
The protein encoded by this gene is a nuclear hormone receptor for triiodothyronine. It is one of the several receptors for thyroid hormone, and has been shown to mediate the biological activities of thyroid hormone. Knockout studies in mice suggest that the different receptors, while having certain extent of redundancy, may mediate different functions of thyroid hormone. Mutations in this gene are known to be a cause of generalized thyroid hormone resistance (GTHR), a syndrome characterized by goiter and high levels of circulating thyroid hormone (T3-T4), with normal or slightly elevated thyroid stimulating hormone (TSH). Several alternatively spliced transcript variants encoding the same protein have been observed for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 27:41695665-41771738
Strand Forward strand
Band
Transcripts
ENSBTAT00000023670 ENSBTAP00000023670
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 55 interaction(s) predicted by orthology.
Predicted by orthology
Total 55 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0003707 steroid hormone receptor activity
GO:0004887 thyroid hormone receptor activity
GO:0005515 protein binding
GO:0008270 zinc ion binding
GO:0019899 enzyme binding
GO:0031490 chromatin DNA binding
GO:0043565 sequence-specific DNA binding
GO:0046872 metal ion binding
GO:0070324 thyroid hormone binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0007605 sensory perception of sound
GO:0007621 negative regulation of female receptivity
GO:0008016 regulation of heart contraction
GO:0008050 female courtship behavior
GO:0009887 organ morphogenesis
GO:0030522 intracellular receptor signaling pathway
GO:0043401 steroid hormone mediated signaling pathway
GO:0045892 negative regulation of transcription, DNA-templated
GO:0045944 positive regulation of transcription from RNA polymerase II promoter
GO:0060509 Type I pneumocyte differentiation
Cellular Component
GO:0000790 nuclear chromatin
GO:0005634 nucleus
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
Prolactin pathway
REACTOME
Nuclear Receptor transcription pathway pathway
Generic Transcription Pathway pathway
Gene Expression pathway
Nuclear Receptor transcription pathway pathway
Gene Expression pathway
Generic Transcription Pathway pathway
KEGG
Neuroactive ligand-receptor interaction pathway
Neuroactive ligand-receptor interaction pathway
INOH
PID NCI
Cross-References
SwissProt
TrEMBL G3X7C1
UniProt Splice Variant
Entrez Gene 788329
UniGene
RefSeq XM_002698755 XM_005226183 XM_005226184 XM_005226185 XM_005226186
HUGO HGNC:11799
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02061150 DAAA02061151 DAAA02061152
GenPept
RNA Seq Atlas 788329