Mus musculus Gene: Stat2
Summary
InnateDB Gene IDBG-197036.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol Stat2
Gene Name signal transducer and activator of transcription 2
Synonyms 1600010G07Rik; AW496480
Species Mus musculus
Ensembl Gene ENSMUSG00000040033
Encoded Proteins
signal transducer and activator of transcription 2
signal transducer and activator of transcription 2
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
InnateDB Annotation
Summary
Transcriptional activation of Adar by IFN occurs in the absence of Stat1 by a non-canonical Stat2-dependent pathway.
InnateDB Annotation from Orthologs
Summary
[Homo sapiens] STAT2 is part of STAT-containing transcription factor, the alpha-interferon-induced ISGF3, that is composed of a STAT1:2 heterodimer and a weak DNA-binding protein, IRF9.
[Homo sapiens] STAT2 is a critical transactivator component of the interferon-stimulated gene factor 3 (ISGF3) complex that drives the expression of many interferon (IFN)-inducible genes.
[Homo sapiens] A loss-of-function mutation in STAT2 is associated with increased susceptibility to childhood viral diseases.
Entrez Gene
Summary This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000170581:
The protein encoded by this gene is a member of the STAT protein family. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. In response to interferon (IFN), this protein forms a complex with STAT1 and IFN regulatory factor family protein p48 (ISGF3G), in which this protein acts as a transactivator, but lacks the ability to bind DNA directly. Transcription adaptor P300/CBP (EP300/CREBBP) has been shown to interact specifically with this protein, which is thought to be involved in the process of blocking IFN-alpha response by adenovirus. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:128270576-128292849
Strand Forward strand
Band D3
Transcripts
ENSMUST00000085708 ENSMUSP00000082855
ENSMUST00000105238 ENSMUSP00000100872
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 48 experimentally validated interaction(s) in this database.
They are also associated with 43 interaction(s) predicted by orthology.
Experimentally validated
Total 48 [view]
Protein-Protein 23 [view]
Protein-DNA 25 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 43 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0004871 signal transducer activity
GO:0005509 calcium ion binding
GO:0005515 protein binding
GO:0042802 identical protein binding
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0007165 signal transduction
GO:0045087 innate immune response (InnateDB)
Cellular Component
GO:0005634 nucleus
GO:0005737 cytoplasm
GO:0005886 plasma membrane
Orthologs
Species
Homo sapiens
Bos taurus
Gene ID
Gene Order
Not yet available
Pathways
NETPATH
REACTOME
KEGG
Jak-STAT signaling pathway pathway
Chemokine signaling pathway pathway
Osteoclast differentiation pathway
Hepatitis C pathway
INOH
PID NCI
Pathway Predictions based on Human Orthology Data
NETPATH
EGFR1 pathway
REACTOME
Regulation of IFNA signaling pathway
Interferon alpha/beta signaling pathway
Cytokine Signaling in Immune system pathway
Interferon Signaling pathway
Immune System pathway
KEGG
Jak-STAT signaling pathway pathway
Chemokine signaling pathway pathway
Osteoclast differentiation pathway
Hepatitis C pathway
INOH
JAK STAT pathway and regulation pathway
IFN alpha signaling pathway
PID NCI
CXCR4-mediated signaling events
IL27-mediated signaling events
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene Mm.293120
RefSeq NM_019963 XM_006513433 XM_006513436
OMIM
CCDS CCDS24269
HPRD
IMGT
MGI ID
MGI Symbol
EMBL
GenPept
RNA Seq Atlas