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Gene: CREB3 |
Gene summary for CREB3 |
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Gene information | Species | Human | Gene symbol | CREB3 | Gene ID | 10488 |
Gene name | cAMP responsive element binding protein 3 | |
Gene Alias | LUMAN | |
Cytomap | 9p13.3 | |
Gene Type | protein-coding | GO ID | GO:0002376 | UniProtAcc | O43889 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10488 | CREB3 | LZE4T | Human | Esophagus | ESCC | 2.91e-06 | 2.74e-01 | 0.0811 |
10488 | CREB3 | LZE5T | Human | Esophagus | ESCC | 1.81e-04 | 2.74e-01 | 0.0514 |
10488 | CREB3 | LZE7T | Human | Esophagus | ESCC | 8.53e-09 | 5.18e-01 | 0.0667 |
10488 | CREB3 | LZE8T | Human | Esophagus | ESCC | 1.57e-09 | 2.79e-01 | 0.067 |
10488 | CREB3 | LZE20T | Human | Esophagus | ESCC | 1.61e-03 | 1.93e-01 | 0.0662 |
10488 | CREB3 | LZE22T | Human | Esophagus | ESCC | 1.32e-03 | 2.47e-01 | 0.068 |
10488 | CREB3 | LZE24T | Human | Esophagus | ESCC | 9.95e-17 | 6.15e-01 | 0.0596 |
10488 | CREB3 | LZE6T | Human | Esophagus | ESCC | 3.10e-02 | 1.16e-01 | 0.0845 |
10488 | CREB3 | P1T-E | Human | Esophagus | ESCC | 7.79e-03 | 2.60e-01 | 0.0875 |
10488 | CREB3 | P2T-E | Human | Esophagus | ESCC | 1.47e-45 | 7.06e-01 | 0.1177 |
10488 | CREB3 | P4T-E | Human | Esophagus | ESCC | 2.32e-18 | 4.41e-01 | 0.1323 |
10488 | CREB3 | P5T-E | Human | Esophagus | ESCC | 2.16e-06 | 1.79e-01 | 0.1327 |
10488 | CREB3 | P8T-E | Human | Esophagus | ESCC | 1.11e-17 | 3.18e-01 | 0.0889 |
10488 | CREB3 | P9T-E | Human | Esophagus | ESCC | 1.82e-10 | 3.47e-01 | 0.1131 |
10488 | CREB3 | P10T-E | Human | Esophagus | ESCC | 2.10e-14 | 3.09e-01 | 0.116 |
10488 | CREB3 | P11T-E | Human | Esophagus | ESCC | 4.89e-20 | 1.06e+00 | 0.1426 |
10488 | CREB3 | P12T-E | Human | Esophagus | ESCC | 4.04e-17 | 3.63e-01 | 0.1122 |
10488 | CREB3 | P15T-E | Human | Esophagus | ESCC | 2.09e-12 | 2.83e-01 | 0.1149 |
10488 | CREB3 | P16T-E | Human | Esophagus | ESCC | 1.32e-16 | 3.65e-01 | 0.1153 |
10488 | CREB3 | P17T-E | Human | Esophagus | ESCC | 4.89e-17 | 6.82e-01 | 0.1278 |
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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:190223624 | Thyroid | PTC | negative regulation of endoplasmic reticulum stress-induced intrinsic apoptotic signaling pathway | 14/5968 | 20/18723 | 5.24e-04 | 3.37e-03 | 14 |
GO:003210316 | Thyroid | PTC | positive regulation of response to external stimulus | 167/5968 | 427/18723 | 8.31e-04 | 5.13e-03 | 167 |
GO:005092115 | Thyroid | PTC | positive regulation of chemotaxis | 62/5968 | 141/18723 | 1.67e-03 | 9.16e-03 | 62 |
GO:000269015 | Thyroid | PTC | positive regulation of leukocyte chemotaxis | 42/5968 | 94/18723 | 6.16e-03 | 2.74e-02 | 42 |
GO:000268718 | Thyroid | PTC | positive regulation of leukocyte migration | 57/5968 | 135/18723 | 7.15e-03 | 3.07e-02 | 57 |
GO:0048193111 | Thyroid | ATC | Golgi vesicle transport | 189/6293 | 296/18723 | 9.58e-27 | 5.05e-24 | 189 |
GO:003497633 | Thyroid | ATC | response to endoplasmic reticulum stress | 167/6293 | 256/18723 | 2.62e-25 | 1.03e-22 | 167 |
GO:200123335 | Thyroid | ATC | regulation of apoptotic signaling pathway | 206/6293 | 356/18723 | 2.81e-21 | 5.92e-19 | 206 |
GO:009719335 | Thyroid | ATC | intrinsic apoptotic signaling pathway | 171/6293 | 288/18723 | 1.86e-19 | 2.67e-17 | 171 |
GO:003596633 | Thyroid | ATC | response to topologically incorrect protein | 102/6293 | 159/18723 | 2.87e-15 | 1.99e-13 | 102 |
GO:200124233 | Thyroid | ATC | regulation of intrinsic apoptotic signaling pathway | 103/6293 | 164/18723 | 1.67e-14 | 9.77e-13 | 103 |
GO:003134623 | Thyroid | ATC | positive regulation of cell projection organization | 186/6293 | 353/18723 | 7.99e-14 | 4.23e-12 | 186 |
GO:2001234210 | Thyroid | ATC | negative regulation of apoptotic signaling pathway | 129/6293 | 224/18723 | 1.26e-13 | 6.46e-12 | 129 |
GO:000698633 | Thyroid | ATC | response to unfolded protein | 88/6293 | 137/18723 | 2.04e-13 | 9.91e-12 | 88 |
GO:000688823 | Thyroid | ATC | endoplasmic reticulum to Golgi vesicle-mediated transport | 84/6293 | 130/18723 | 4.40e-13 | 1.97e-11 | 84 |
GO:000150332 | Thyroid | ATC | ossification | 206/6293 | 408/18723 | 9.23e-13 | 3.95e-11 | 206 |
GO:003596733 | Thyroid | ATC | cellular response to topologically incorrect protein | 74/6293 | 116/18723 | 2.69e-11 | 9.20e-10 | 74 |
GO:001097523 | Thyroid | ATC | regulation of neuron projection development | 212/6293 | 445/18723 | 4.16e-10 | 1.14e-08 | 212 |
GO:200124333 | Thyroid | ATC | negative regulation of intrinsic apoptotic signaling pathway | 63/6293 | 98/18723 | 4.97e-10 | 1.33e-08 | 63 |
GO:000164932 | Thyroid | ATC | osteoblast differentiation | 122/6293 | 229/18723 | 6.04e-10 | 1.60e-08 | 122 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa05016210 | Esophagus | ESCC | Huntington disease | 226/4205 | 306/8465 | 1.38e-18 | 8.72e-17 | 4.46e-17 | 226 |
hsa05166211 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
hsa05020210 | Esophagus | ESCC | Prion disease | 193/4205 | 273/8465 | 6.42e-13 | 1.34e-11 | 6.89e-12 | 193 |
hsa04714211 | Esophagus | ESCC | Thermogenesis | 163/4205 | 232/8465 | 9.22e-11 | 1.14e-09 | 5.86e-10 | 163 |
hsa0466810 | Esophagus | ESCC | TNF signaling pathway | 89/4205 | 114/8465 | 3.36e-10 | 4.01e-09 | 2.06e-09 | 89 |
hsa0516510 | Esophagus | ESCC | Human papillomavirus infection | 215/4205 | 331/8465 | 7.86e-09 | 7.12e-08 | 3.65e-08 | 215 |
hsa0520325 | Esophagus | ESCC | Viral carcinogenesis | 137/4205 | 204/8465 | 2.47e-07 | 1.88e-06 | 9.62e-07 | 137 |
hsa05163210 | Esophagus | ESCC | Human cytomegalovirus infection | 148/4205 | 225/8465 | 5.73e-07 | 4.00e-06 | 2.05e-06 | 148 |
hsa0521516 | Esophagus | ESCC | Prostate cancer | 72/4205 | 97/8465 | 6.12e-07 | 4.10e-06 | 2.10e-06 | 72 |
hsa051619 | Esophagus | ESCC | Hepatitis B | 108/4205 | 162/8465 | 7.68e-06 | 4.15e-05 | 2.12e-05 | 108 |
hsa0415210 | Esophagus | ESCC | AMPK signaling pathway | 80/4205 | 121/8465 | 1.73e-04 | 6.67e-04 | 3.42e-04 | 80 |
hsa0496223 | Esophagus | ESCC | Vasopressin-regulated water reabsorption | 33/4205 | 44/8465 | 5.27e-04 | 1.78e-03 | 9.13e-04 | 33 |
hsa049268 | Esophagus | ESCC | Relaxin signaling pathway | 81/4205 | 129/8465 | 1.72e-03 | 5.09e-03 | 2.61e-03 | 81 |
hsa049318 | Esophagus | ESCC | Insulin resistance | 69/4205 | 108/8465 | 1.92e-03 | 5.54e-03 | 2.84e-03 | 69 |
hsa0421114 | Esophagus | ESCC | Longevity regulating pathway | 58/4205 | 89/8465 | 2.19e-03 | 6.16e-03 | 3.16e-03 | 58 |
hsa0492816 | Esophagus | ESCC | Parathyroid hormone synthesis, secretion and action | 66/4205 | 106/8465 | 5.86e-03 | 1.47e-02 | 7.51e-03 | 66 |
hsa041517 | Esophagus | ESCC | PI3K-Akt signaling pathway | 197/4205 | 354/8465 | 1.24e-02 | 2.83e-02 | 1.45e-02 | 197 |
hsa0492214 | Esophagus | ESCC | Glucagon signaling pathway | 64/4205 | 107/8465 | 2.18e-02 | 4.80e-02 | 2.46e-02 | 64 |
hsa0501638 | Esophagus | ESCC | Huntington disease | 226/4205 | 306/8465 | 1.38e-18 | 8.72e-17 | 4.46e-17 | 226 |
hsa05166310 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
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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 |
CREB3 | SNV | Missense_Mutation | c.46N>A | p.Leu16Met | p.L16M | O43889 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A2-A04U-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | |
CREB3 | SNV | Missense_Mutation | novel | c.916N>A | p.Gly306Ser | p.G306S | O43889 | protein_coding | tolerated(0.39) | benign(0.041) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
CREB3 | SNV | Missense_Mutation | c.710C>T | p.Ser237Phe | p.S237F | O43889 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-Q1-A5R1-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | |
CREB3 | SNV | Missense_Mutation | rs754545426 | c.499N>G | p.Ser167Gly | p.S167G | O43889 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-AD-6965-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | oxaliplatin | PD |
CREB3 | SNV | Missense_Mutation | c.799C>T | p.Arg267Cys | p.R267C | O43889 | protein_coding | deleterious(0) | probably_damaging(0.987) | TCGA-AY-A71X-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
CREB3 | SNV | Missense_Mutation | c.134N>G | p.Pro45Arg | p.P45R | O43889 | protein_coding | tolerated(0.16) | benign(0.32) | TCGA-AG-3894-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Chemotherapy | 5-fluorouracil | CR | |
CREB3 | SNV | Missense_Mutation | c.290N>A | p.Cys97Tyr | p.C97Y | O43889 | protein_coding | tolerated(1) | benign(0) | TCGA-EI-6509-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD | |
CREB3 | SNV | Missense_Mutation | novel | c.447N>C | p.Gln149His | p.Q149H | O43889 | protein_coding | deleterious(0.03) | benign(0.198) | TCGA-F5-6814-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
CREB3 | deletion | Frame_Shift_Del | c.178delN | p.Pro61GlnfsTer4 | p.P61Qfs*4 | O43889 | protein_coding | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |||
CREB3 | deletion | Frame_Shift_Del | novel | c.282_285delTGAG | p.Ser94ArgfsTer10 | p.S94Rfs*10 | O43889 | protein_coding | TCGA-AA-3845-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
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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 |
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