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Gene: HSF1 |
Gene summary for HSF1 |
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Gene information | Species | Human | Gene symbol | HSF1 | Gene ID | 3297 |
Gene name | heat shock transcription factor 1 | |
Gene Alias | HSTF1 | |
Cytomap | 8q24.3 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q00613 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
3297 | HSF1 | P104T-E | Human | Esophagus | ESCC | 1.19e-03 | 9.47e-01 | 0.0931 |
3297 | HSF1 | P107T-E | Human | Esophagus | ESCC | 4.31e-94 | 2.77e+00 | 0.171 |
3297 | HSF1 | P126T-E | Human | Esophagus | ESCC | 2.32e-12 | 1.82e+00 | 0.1125 |
3297 | HSF1 | P127T-E | Human | Esophagus | ESCC | 9.54e-26 | 4.66e-01 | 0.0826 |
3297 | HSF1 | P128T-E | Human | Esophagus | ESCC | 3.74e-72 | 3.18e+00 | 0.1241 |
3297 | HSF1 | P130T-E | Human | Esophagus | ESCC | 3.69e-103 | 2.12e+00 | 0.1676 |
3297 | HSF1 | HCC1_Meng | Human | Liver | HCC | 3.56e-90 | 2.35e-01 | 0.0246 |
3297 | HSF1 | HCC2_Meng | Human | Liver | HCC | 2.72e-36 | 1.72e-01 | 0.0107 |
3297 | HSF1 | cirrhotic2 | Human | Liver | Cirrhotic | 9.05e-07 | 1.07e-01 | 0.0201 |
3297 | HSF1 | HCC1 | Human | Liver | HCC | 4.91e-07 | 3.60e+00 | 0.5336 |
3297 | HSF1 | HCC2 | Human | Liver | HCC | 4.67e-21 | 4.37e+00 | 0.5341 |
3297 | HSF1 | Pt13.b | Human | Liver | HCC | 2.10e-27 | 3.80e-01 | 0.0251 |
3297 | HSF1 | Pt14.a | Human | Liver | HCC | 4.41e-04 | 2.57e-01 | 0.0169 |
3297 | HSF1 | Pt14.b | Human | Liver | HCC | 9.36e-05 | 2.49e-01 | 0.018 |
3297 | HSF1 | S014 | Human | Liver | HCC | 2.21e-65 | 2.44e+00 | 0.2254 |
3297 | HSF1 | S015 | Human | Liver | HCC | 2.48e-61 | 2.65e+00 | 0.2375 |
3297 | HSF1 | S016 | Human | Liver | HCC | 1.96e-82 | 2.52e+00 | 0.2243 |
3297 | HSF1 | S027 | Human | Liver | HCC | 1.03e-28 | 2.32e+00 | 0.2446 |
3297 | HSF1 | S028 | Human | Liver | HCC | 7.26e-56 | 2.63e+00 | 0.2503 |
3297 | HSF1 | S029 | Human | Liver | HCC | 1.90e-47 | 2.72e+00 | 0.2581 |
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∗log2FC in expression of this searched gene in stem-like cells from each diseased tissue sample relative to stem-like cells in normal samples in each tissue plotted against the malignancy continuum. Samples are colored based on if they are from different disease stage. |
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Malignant transformation related pathway analysis |
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Tissue | Disease Stage | Enriched GO biological Processes |
Colorectum | AD | ![]() |
Colorectum | SER | ![]() |
Colorectum | MSS | ![]() |
Colorectum | MSI-H | ![]() |
Colorectum | FAP | ![]() |
∗Top 15 enriched GO BP terms are showed in the bar plot of each disease state in each tissue. Each row represents a significant GO biological process which is colored according to the -log10(p.adjust). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:190331120 | Esophagus | HGIN | regulation of mRNA metabolic process | 91/2587 | 288/18723 | 5.06e-15 | 9.78e-13 | 91 |
GO:005068419 | Esophagus | HGIN | regulation of mRNA processing | 55/2587 | 137/18723 | 2.17e-14 | 3.94e-12 | 55 |
GO:004586227 | Esophagus | HGIN | positive regulation of proteolysis | 107/2587 | 372/18723 | 2.61e-14 | 4.60e-12 | 107 |
GO:000989626 | Esophagus | HGIN | positive regulation of catabolic process | 126/2587 | 492/18723 | 1.46e-12 | 2.09e-10 | 126 |
GO:000640320 | Esophagus | HGIN | RNA localization | 66/2587 | 201/18723 | 4.06e-12 | 5.41e-10 | 66 |
GO:003133126 | Esophagus | HGIN | positive regulation of cellular catabolic process | 112/2587 | 427/18723 | 5.15e-12 | 6.72e-10 | 112 |
GO:003596625 | Esophagus | HGIN | response to topologically incorrect protein | 54/2587 | 159/18723 | 8.53e-11 | 8.89e-09 | 54 |
GO:000698625 | Esophagus | HGIN | response to unfolded protein | 48/2587 | 137/18723 | 2.80e-10 | 2.54e-08 | 48 |
GO:003460520 | Esophagus | HGIN | cellular response to heat | 30/2587 | 69/18723 | 1.78e-09 | 1.35e-07 | 30 |
GO:000697927 | Esophagus | HGIN | response to oxidative stress | 107/2587 | 446/18723 | 3.91e-09 | 2.76e-07 | 107 |
GO:003596725 | Esophagus | HGIN | cellular response to topologically incorrect protein | 41/2587 | 116/18723 | 4.07e-09 | 2.84e-07 | 41 |
GO:003462020 | Esophagus | HGIN | cellular response to unfolded protein | 36/2587 | 96/18723 | 5.82e-09 | 3.88e-07 | 36 |
GO:003465519 | Esophagus | HGIN | nucleobase-containing compound catabolic process | 98/2587 | 407/18723 | 1.44e-08 | 8.94e-07 | 98 |
GO:004328126 | Esophagus | HGIN | regulation of cysteine-type endopeptidase activity involved in apoptotic process | 59/2587 | 209/18723 | 3.39e-08 | 1.97e-06 | 59 |
GO:004670017 | Esophagus | HGIN | heterocycle catabolic process | 103/2587 | 445/18723 | 5.44e-08 | 2.99e-06 | 103 |
GO:005065716 | Esophagus | HGIN | nucleic acid transport | 49/2587 | 163/18723 | 5.71e-08 | 3.06e-06 | 49 |
GO:005065816 | Esophagus | HGIN | RNA transport | 49/2587 | 163/18723 | 5.71e-08 | 3.06e-06 | 49 |
GO:002241120 | Esophagus | HGIN | cellular component disassembly | 102/2587 | 443/18723 | 8.31e-08 | 4.33e-06 | 102 |
GO:200011626 | Esophagus | HGIN | regulation of cysteine-type endopeptidase activity | 63/2587 | 235/18723 | 9.71e-08 | 5.02e-06 | 63 |
GO:005123616 | Esophagus | HGIN | establishment of RNA localization | 49/2587 | 166/18723 | 1.07e-07 | 5.47e-06 | 49 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0513427 | Esophagus | HGIN | Legionellosis | 18/1383 | 57/8465 | 3.20e-03 | 2.54e-02 | 2.02e-02 | 18 |
hsa05134112 | Esophagus | HGIN | Legionellosis | 18/1383 | 57/8465 | 3.20e-03 | 2.54e-02 | 2.02e-02 | 18 |
hsa0513428 | Esophagus | ESCC | Legionellosis | 42/4205 | 57/8465 | 1.83e-04 | 6.90e-04 | 3.53e-04 | 42 |
hsa0513436 | Esophagus | ESCC | Legionellosis | 42/4205 | 57/8465 | 1.83e-04 | 6.90e-04 | 3.53e-04 | 42 |
hsa0513412 | Liver | Cirrhotic | Legionellosis | 28/2530 | 57/8465 | 1.71e-03 | 8.01e-03 | 4.94e-03 | 28 |
hsa0513413 | Liver | Cirrhotic | Legionellosis | 28/2530 | 57/8465 | 1.71e-03 | 8.01e-03 | 4.94e-03 | 28 |
hsa0513425 | Oral cavity | OSCC | Legionellosis | 42/3704 | 57/8465 | 4.18e-06 | 2.15e-05 | 1.10e-05 | 42 |
hsa05134111 | Oral cavity | OSCC | Legionellosis | 42/3704 | 57/8465 | 4.18e-06 | 2.15e-05 | 1.10e-05 | 42 |
hsa0513426 | Oral cavity | LP | Legionellosis | 33/2418 | 57/8465 | 3.29e-06 | 3.23e-05 | 2.08e-05 | 33 |
hsa0513435 | Oral cavity | LP | Legionellosis | 33/2418 | 57/8465 | 3.29e-06 | 3.23e-05 | 2.08e-05 | 33 |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
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∗The dot plots of a searched regulon are shown for all cell subpopulations in each disease state of each tissue based on the regulon specific score inferred using pySCENIC and by calculating the average expression. |
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Somatic mutation of malignant transformation related genes |
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Hugo Symbol | Variant Class | Variant Classification | dbSNP RS | HGVSc | HGVSp | HGVSp Short | SWISSPROT | BIOTYPE | SIFT | PolyPhen | Tumor Sample Barcode | Tissue | Histology | Sex | Age | Stage | Therapy Types | Drugs | Outcome |
HSF1 | SNV | Missense_Mutation | c.1477N>A | p.Glu493Lys | p.E493K | Q00613 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A2-A0SY-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Hormone Therapy | arimidex | SD | |
HSF1 | SNV | Missense_Mutation | rs781942523 | c.526N>T | p.Arg176Trp | p.R176W | Q00613 | protein_coding | deleterious(0.01) | benign(0.063) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
HSF1 | SNV | Missense_Mutation | rs781942523 | c.526C>T | p.Arg176Trp | p.R176W | Q00613 | protein_coding | deleterious(0.01) | benign(0.063) | TCGA-C8-A3M7-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
HSF1 | SNV | Missense_Mutation | c.606N>G | p.Ile202Met | p.I202M | Q00613 | protein_coding | deleterious(0.02) | probably_damaging(0.925) | TCGA-E2-A156-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | arimidex | SD | |
HSF1 | SNV | Missense_Mutation | c.141C>G | p.Phe47Leu | p.F47L | Q00613 | protein_coding | tolerated(0.14) | benign(0.053) | TCGA-E2-A1B6-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Adriamycin | SD | |
HSF1 | SNV | Missense_Mutation | rs377258216 | c.1051N>A | p.Ala351Thr | p.A351T | Q00613 | protein_coding | tolerated(0.49) | benign(0.001) | TCGA-EX-A8YF-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD |
HSF1 | SNV | Missense_Mutation | c.582N>G | p.Ile194Met | p.I194M | Q00613 | protein_coding | deleterious(0.02) | possibly_damaging(0.779) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
HSF1 | SNV | Missense_Mutation | rs782078876 | c.1409C>T | p.Ala470Val | p.A470V | Q00613 | protein_coding | deleterious(0.02) | probably_damaging(0.962) | TCGA-A6-5661-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
HSF1 | SNV | Missense_Mutation | c.1259N>T | p.Pro420Leu | p.P420L | Q00613 | protein_coding | deleterious(0.03) | possibly_damaging(0.851) | TCGA-CM-6165-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
HSF1 | SNV | Missense_Mutation | c.257N>G | p.Gln86Arg | p.Q86R | Q00613 | protein_coding | deleterious(0.03) | probably_damaging(0.999) | TCGA-DM-A1HB-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
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(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
3297 | HSF1 | TRANSCRIPTION FACTOR, DNA REPAIR | QUERCETIN | QUERCETIN | 19296652 | |
3297 | HSF1 | TRANSCRIPTION FACTOR, DNA REPAIR | CYCLOHEXIMIDE | CYCLOHEXIMIDE | ||
3297 | HSF1 | TRANSCRIPTION FACTOR, DNA REPAIR | BIMOCLOMOL | BIMOCLOMOL | ||
3297 | HSF1 | TRANSCRIPTION FACTOR, DNA REPAIR | HSP70 | 9499401,9822662 |
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