protein
| interaction between STAT6 and CREBBP was found to be mediated through SND1  |
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SPIC interacted specifically with the C-terminus of STAT6 (interaction between SPIC and STAT6 is the basis for a novel mechanism for regulation of IL4 induced gene expression) |
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phosphorylated STAT6 may serve as a cytoplasmic substrate for PTPN1 (interacted with STAT6 in an interleukin 4 (IL4)-inducible manner, and negative regulator of interleukin 4-induced STAT6 signaling) |
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binds the ACP5 promoter after IL4 treatment and directly enhances its expression)  |
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STAT6 and JUN proteins were found to physically cooperate with each other and upregulated IL24 gene transcription  |
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PKD1 cytoplasmic tail associates with the transcription factors TPX2 and STAT6  |
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IL4-activated STAT6 is required for repressing the expression of T-bet and FOXP3 in Th9 cells, transcription factors that inhibit IL9 production, and STAT6 is required for the induction of IRF4, which promotes Th9 development  |
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TYK2 controls STAT1 and STAT6 activation in response to IL13 stimulation  |
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the gene fusion can convert a transcriptional repressor (NAB2) into a transcriptional activator (NAB2-STAT6) of mitogenic pathways that can be subverted during neoplastic progression  |
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while IL4 inhibits and activates different sets of lysosomal genes, STAT6 mediates only the activating effects of IL4, by promoting increased expression and by neutralizing undefined inhibitory signals induced by IL4  |
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IL4 increases the binding of STAT6 to its response elements in the IL19 promoter  |
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CBLB suppresses ORMDL3 expression through STAT6  |
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TMEM173 promoted the transcriptional activity of ORMDL3, which was significantly associated with increased levels of interferon regulatory factor 3 (IRF3) and signal transducer and activator of transcription 6 (STAT6)  |