Homo sapiens Protein: STAT4 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-245896.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | STAT4 | ||||||||||||||||||||||
Protein Name | signal transducer and activator of transcription 4 | ||||||||||||||||||||||
Synonyms | SLEB11; | ||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000376134 | ||||||||||||||||||||||
InnateDB Gene | IDBG-77625 (STAT4) | ||||||||||||||||||||||
Protein Structure | |||||||||||||||||||||||
UniProt Annotation | |||||||||||||||||||||||
Function | Carries out a dual function: signal transduction and activation of transcription. Involved in IL12 signaling. | ||||||||||||||||||||||
Subcellular Localization | Cytoplasm. Nucleus. Note=Translocated into the nucleus in response to phosphorylation. | ||||||||||||||||||||||
Disease Associations | Systemic lupus erythematosus 11 (SLEB11) [MIM:612253]: A chronic, relapsing, inflammatory, and often febrile multisystemic disorder of connective tissue, characterized principally by involvement of the skin, joints, kidneys and serosal membranes. It is of unknown etiology, but is thought to represent a failure of the regulatory mechanisms of the autoimmune system. The disease is marked by a wide range of system dysfunctions, an elevated erythrocyte sedimentation rate, and the formation of LE cells in the blood or bone marrow. {ECO:0000269PubMed:19109131}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.Rheumatoid arthritis (RA) [MIM:180300]: An inflammatory disease with autoimmune features and a complex genetic component. It primarily affects the joints and is characterized by inflammatory changes in the synovial membranes and articular structures, widespread fibrinoid degeneration of the collagen fibers in mesenchymal tissues, and by atrophy and rarefaction of bony structures. {ECO:0000269PubMed:17804842}. Note=Disease susceptibility is associated with variations affecting the gene represented in this entry. | ||||||||||||||||||||||
Tissue Specificity | |||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 21 experimentally validated interaction(s) in this database.
They are also associated with 10 interaction(s) predicted by orthology.
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Gene Ontology | |||||||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||||||
PDB ID | |||||||||||||||||||||||
InterPro |
IPR000980
SH2 domain IPR008967 p53-like transcription factor, DNA-binding IPR013799 STAT transcription factor, protein interaction IPR013800 STAT transcription factor, all-alpha IPR013801 STAT transcription factor, DNA-binding IPR015988 STAT transcription factor, coiled coil |
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PFAM |
PF00017
PF14633 PF02865 PF01017 PF02864 |
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PRINTS |
PR00401
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PIRSF | |||||||||||||||||||||||
SMART |
SM00252
SM00964 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | Q14765 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-Q14765 | ||||||||||||||||||||||
TrEMBL | Q53S87 | ||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 6775 | ||||||||||||||||||||||
UniGene | Hs.80642 | ||||||||||||||||||||||
RefSeq | NP_003142 | ||||||||||||||||||||||
HUGO | HGNC:11365 | ||||||||||||||||||||||
OMIM | 600558 | ||||||||||||||||||||||
CCDS | CCDS2310 | ||||||||||||||||||||||
HPRD | 02779 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AC067945 AC079777 AF423072 BC031212 EU304788 EU304789 EU304790 EU304791 EU304792 EU304793 L78440 | ||||||||||||||||||||||
GenPept | AAB05605 AAH31212 AAL12164 AAY15055 AAY24184 ACA01857 ACA01858 ACA01859 ACA01860 ACA01861 ACA01862 | ||||||||||||||||||||||