Bos taurus Gene: BT.89909
Summary
InnateDB Gene IDBG-642936.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol BT.89909
Gene Name 60 kDa heat shock protein, mitochondrial
Synonyms HSP60
Species Bos taurus
Ensembl Gene ENSBTAG00000012586
Encoded Proteins
60 kDa heat shock protein, mitochondrial
60 kDa heat shock protein, mitochondrial
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation from Orthologs
Summary
[Homo sapiens] HSPD1 is part of the heat shock family of proteins that have many roles in inflammation and regulation of the immune system.
[Homo sapiens] HSPD1 plays a dual role as an immune modulator and a biomarker, and is a target to modulate immunity for therapeutic purposes, and to monitor the immune response in health and disease.
[Homo sapiens] HSPD1 and TLR4 mediate myocardial ischemia-activated innate immune signalling, which plays an important role in mediating apoptosis and inflammation during ischemia/reperfusion (I/R). (Demonstrated in murine model)
[Mus musculus] Hspd1 plays a dual role as an immune modulator and a biomarker, and is a target to modulate immunity for therapeutic purposes, and to monitor the immune response in health and disease.
[Mus musculus] Hspd1 and Tlr4 mediate myocardial ischemia-activated innate immune signalling, which plays an important role in mediating apoptosis and inflammation during ischemia/reperfusion (I/R).
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000144381:
This gene encodes a member of the chaperonin family. The encoded mitochondrial protein may function as a signaling molecule in the innate immune system. This protein is essential for the folding and assembly of newly imported proteins in the mitochondria. This gene is adjacent to a related family member and the region between the 2 genes functions as a bidirectional promoter. Several pseudogenes have been associated with this gene. Two transcript variants encoding the same protein have been identified for this gene. Mutations associated with this gene cause autosomal recessive spastic paraplegia 13. [provided by RefSeq, Jun 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 2:86438979-86449372
Strand Reverse strand
Band
Transcripts
ENSBTAT00000064253 ENSBTAP00000055431
ENSBTAT00000016708 ENSBTAP00000016708
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 115 interaction(s) predicted by orthology.
Predicted by orthology
Total 115 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000166 nucleotide binding
GO:0001530 lipopolysaccharide binding
GO:0002039 p53 binding
GO:0003725 double-stranded RNA binding
GO:0005515 protein binding
GO:0005524 ATP binding
GO:0044822 poly(A) RNA binding
GO:0051087 chaperone binding
Biological Process
GO:0002368 B cell cytokine production
GO:0002755 MyD88-dependent toll-like receptor signaling pathway
GO:0002842 positive regulation of T cell mediated immune response to tumor cell
GO:0006457 protein folding
GO:0006919 activation of cysteine-type endopeptidase activity involved in apoptotic process
GO:0006986 response to unfolded protein
GO:0032727 positive regulation of interferon-alpha production
GO:0032729 positive regulation of interferon-gamma production
GO:0032733 positive regulation of interleukin-10 production
GO:0032735 positive regulation of interleukin-12 production
GO:0032755 positive regulation of interleukin-6 production
GO:0042026 protein refolding
GO:0042100 B cell proliferation
GO:0042110 T cell activation
GO:0042113 B cell activation
GO:0043032 positive regulation of macrophage activation
GO:0043065 positive regulation of apoptotic process
GO:0043066 negative regulation of apoptotic process
GO:0044267 cellular protein metabolic process
GO:0048291 isotype switching to IgG isotypes
GO:0050870 positive regulation of T cell activation
Cellular Component
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0005769 early endosome
GO:0005829 cytosol
GO:0005886 plasma membrane
GO:0005905 coated pit
GO:0009986 cell surface
GO:0016020 membrane
GO:0019907 cyclin-dependent protein kinase activating kinase holoenzyme complex
GO:0030135 coated vesicle
GO:0030141 secretory granule
GO:0043231 intracellular membrane-bounded organelle
GO:0043234 protein complex
GO:0046696 lipopolysaccharide receptor complex
GO:0070062 extracellular vesicular exosome
Orthologs
Species
Homo sapiens
Mus musculus
Gene ID
Gene Order
Pathway Predictions based on Human Orthology Data
NETPATH
REACTOME
Mitochondrial protein import pathway
Metabolism of proteins pathway
Metabolism of proteins pathway
Mitochondrial protein import pathway
KEGG
Type I diabetes mellitus pathway
RNA degradation pathway
Type I diabetes mellitus pathway
RNA degradation pathway
INOH
PID NCI
Validated targets of C-MYC transcriptional activation
Endogenous TLR signaling
Cross-References
SwissProt
TrEMBL F1MUZ9
UniProt Splice Variant
Entrez Gene 511913
UniGene Bt.24270 Bt.89909
RefSeq NM_001166608 NM_001166609 NM_001166610 XM_005202627
HUGO HGNC:5261
OMIM
CCDS
HPRD
IMGT
EMBL DAAA02005515
GenPept
RNA Seq Atlas 511913