Basic information

Full name
heat shock transcription factor 4
Ensembl
ENSG00000102878.17
Summary
Heat-shock transcription factors (HSFs) activate heat-shock response genes under conditions of heat or other stresses. HSF4 lacks the carboxyl-terminal hydrophobic repeat which is shared among all vertebrate HSFs and has been suggested to be involved in the negative regulation of DNA binding activity. Two alternatively spliced transcripts encoding distinct isoforms and possessing different transcriptional activity have been described. [provided by RefSeq, Jul 2008]
Annotation
Transcription factor

Protein product

Phosphosites on the primary protein product
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Tumor and normal comparison

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Signed p-values
Data type
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
RNA0.039-2.6e-28---1.1e-7-4.8e-32.4e-9--0.15-
protein0.95-0.95--------

* P-values are from Wilcoxon rank sum test and can be clicked to show the box plots. Positive values mean higher abundance in tumor. BRCA and GBM do not have normal samples.

mRNA expression at gene level
BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC2345678910111213log2(RSEM+1)tumornormal
Protein expression
CCRCC18.618.81919.219.419.619.82020.220.420.620.821log2(MS1 intensity)tumornormal

* Mild outlier: filled circle; Extreme outlier: empty circle.

Phenotype and mutation association

Manhattan plot summarizing associations of phenotypes and mutations across all cohorts and omics data types

BRCACCRCCCOADGBMHNSCCLSCCLUADOVPDACUCEC0123456789100-1-2-3-4-5-6-7-8-9-10Pan-cancer024681012141618202224260-2-4-6-8-10-12-14-16-18-20-22-24-26proteinRNASCNVclinicalpathwaycell typegenomicmutation-log10 of P-value

* Data points of significant associations above and below the dotted lines can be hovered to show the phenotype.

Associations of the protein abundance of HSF4 with phenotypes and mutations

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Signed p-values
Phenotype
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
HALLMARK_KRAS_SIGNALING_DN0.021-0.021--------
Tumor Purity (WGS)0.026-0.026--------
cibersort: Myeloid dendritic cell activated0.041-0.041--------
xcell: Common lymphoid progenitor0.047-0.047--------
Tumor Purity (ABSOLUTE)0.075-0.075--------
PROGENy: Hypoxia0.076-0.076--------
xcell: Hematopoietic stem cell0.084-0.084--------
PROGENy: Androgen0.1-0.1--------
xcell: B cell naive0.12-0.12--------
chromosomal instability0.14-0.14--------
Showing 1 to 10 of 256 rows

* P-values could be from test for Spearman correlation, Wilcoxon rank sum test, Jonckheere-Terpstra trend test or Cox regression depending on the data type. P-values for individual cohorts can be clicked to show the data plots. The matrix icons in each row can be clicked to show a heatmap summary of associations across all cohorts and omics. The rows in the table can be expanded to show results from other omics.

Cis-association

Associations between omics data of HSF4

BRCA0.28proteinmRNASCNVmethylationCCRCC0.42-0.35-0.17-0.290.07-0.06proteinmRNASCNVmethylationCOAD0.30proteinmRNASCNVmethylationGBM-0.030.210.03proteinmRNASCNVmethylationHNSCC-0.050.320.03proteinmRNASCNVmethylationLSCC0.140.450.20proteinmRNASCNVmethylationLUAD-0.040.540.00proteinmRNASCNVmethylationOV0.53proteinmRNASCNVmethylationPDAC0.070.18-0.00proteinmRNASCNVmethylationUCEC-0.100.190.01proteinmRNASCNVmethylation

* The numbers are Spearman correlation coefficients and can be clicked to show the scatter plots. The color and size of the circles correlate with the coefficients.

Trans-association

Associations of the protein abundance of HSF4 and the protein abundance of other genes

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Signed p-values
Gene
Meta P
BRCA
CCRCC
COAD
GBM
HNSCC
LSCC
LUAD
OV
PDAC
UCEC
No matching records found

* P-values are from test for Spearman correlation. P-values for individual cohorts can be clicked to show the data plots. The matrix icons in each row can be clicked to show a heatmap summary of associations across all cohorts and omics. The rows in the table can be expanded to show results from other omics.

Gene set enrichment analysis

Submit genes and the common logarithm of the p-values of their association with to WebGestalt.