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Gene: CREM |
Gene summary for CREM |
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Gene information | Species | Human | Gene symbol | CREM | Gene ID | 1390 |
Gene name | cAMP responsive element modulator | |
Gene Alias | CREM-2 | |
Cytomap | 10p11.21 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | Q03060 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
1390 | CREM | LN46 | Human | Oral cavity | OSCC | 1.47e-07 | 6.85e-01 | 0.1666 |
1390 | CREM | EOLP-1 | Human | Oral cavity | EOLP | 6.14e-17 | 2.25e-01 | -0.0202 |
1390 | CREM | EOLP-2 | Human | Oral cavity | EOLP | 6.47e-03 | 1.00e-01 | -0.0203 |
1390 | CREM | NEOLP-3 | Human | Oral cavity | NEOLP | 4.21e-03 | 1.45e-01 | -0.0191 |
1390 | CREM | SYSMH1 | Human | Oral cavity | OSCC | 4.36e-21 | -6.27e-01 | 0.1127 |
1390 | CREM | SYSMH2 | Human | Oral cavity | OSCC | 8.88e-15 | -3.28e-01 | 0.2326 |
1390 | CREM | SYSMH3 | Human | Oral cavity | OSCC | 1.01e-17 | -5.51e-01 | 0.2442 |
1390 | CREM | SYSMH4 | Human | Oral cavity | OSCC | 1.23e-19 | -7.52e-01 | 0.1226 |
1390 | CREM | SYSMH5 | Human | Oral cavity | OSCC | 9.37e-17 | -7.53e-01 | 0.0647 |
1390 | CREM | SYSMH6 | Human | Oral cavity | OSCC | 4.74e-26 | -5.75e-01 | 0.1275 |
1390 | CREM | HTA12-15-2 | Human | Pancreas | PDAC | 2.79e-04 | 5.02e-01 | 0.2315 |
1390 | CREM | HTA12-29-1 | Human | Pancreas | PDAC | 1.06e-08 | 3.06e-01 | 0.3722 |
1390 | CREM | HTA12-9-2 | Human | Pancreas | PDAC | 3.96e-07 | 6.61e-01 | 0.0835 |
1390 | CREM | GSM5252126_BPH283PrGF_Via | Human | Prostate | BPH | 1.77e-07 | 5.71e-01 | -0.1771 |
1390 | CREM | GSM5252127_BPH283PrSF_Via | Human | Prostate | BPH | 1.06e-04 | 7.14e-01 | -0.1453 |
1390 | CREM | GSM5252128_BPH327PrGF_Via | Human | Prostate | BPH | 3.41e-04 | 4.35e-01 | -0.1688 |
1390 | CREM | GSM5252129_BPH327PrSF_Via | Human | Prostate | BPH | 8.25e-03 | 7.86e-01 | -0.1697 |
1390 | CREM | GSM5252130_BPH340PrGF_Via | Human | Prostate | BPH | 4.84e-06 | 5.29e-01 | -0.1972 |
1390 | CREM | GSM5252131_BPH340PrSF_Via | Human | Prostate | BPH | 5.10e-18 | 1.06e+00 | -0.2126 |
1390 | CREM | GSM5252132_BPH389PrGF | Human | Prostate | BPH | 3.35e-03 | 6.77e-01 | -0.2247 |
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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:004851118 | Esophagus | ESCC | rhythmic process | 164/8552 | 298/18723 | 6.80e-04 | 3.57e-03 | 164 |
GO:00485115 | Liver | NAFLD | rhythmic process | 56/1882 | 298/18723 | 3.03e-06 | 1.23e-04 | 56 |
GO:004851111 | Liver | Cirrhotic | rhythmic process | 103/4634 | 298/18723 | 8.47e-05 | 9.19e-04 | 103 |
GO:004851121 | Liver | HCC | rhythmic process | 156/7958 | 298/18723 | 3.54e-04 | 2.46e-03 | 156 |
GO:004851116 | Oral cavity | OSCC | rhythmic process | 157/7305 | 298/18723 | 1.00e-06 | 1.36e-05 | 157 |
GO:004851117 | Oral cavity | EOLP | rhythmic process | 69/2218 | 298/18723 | 2.68e-08 | 1.11e-06 | 69 |
GO:004851122 | Oral cavity | NEOLP | rhythmic process | 60/2005 | 298/18723 | 1.02e-06 | 2.72e-05 | 60 |
GO:004851110 | Prostate | BPH | rhythmic process | 96/3107 | 298/18723 | 1.88e-11 | 1.31e-09 | 96 |
GO:004851115 | Prostate | Tumor | rhythmic process | 99/3246 | 298/18723 | 1.65e-11 | 1.21e-09 | 99 |
GO:004851120 | Thyroid | HT | rhythmic process | 41/1272 | 298/18723 | 1.26e-05 | 3.27e-04 | 41 |
GO:0048511111 | Thyroid | PTC | rhythmic process | 131/5968 | 298/18723 | 7.06e-06 | 8.33e-05 | 131 |
GO:004851124 | Thyroid | ATC | rhythmic process | 141/6293 | 298/18723 | 5.58e-07 | 7.93e-06 | 141 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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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 |
CREM | SNV | Missense_Mutation | c.835N>G | p.Gln279Glu | p.Q279E | Q03060 | protein_coding | deleterious(0) | probably_damaging(0.989) | TCGA-BH-A0BZ-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | CR | |
CREM | SNV | Missense_Mutation | novel | c.608N>T | p.Gly203Val | p.G203V | Q03060 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-OL-A5RW-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | CR |
CREM | SNV | Missense_Mutation | c.786N>T | p.Lys262Asn | p.K262N | Q03060 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
CREM | SNV | Missense_Mutation | c.647N>T | p.Ala216Val | p.A216V | Q03060 | protein_coding | tolerated(0.07) | benign(0.304) | TCGA-AA-3864-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
CREM | SNV | Missense_Mutation | novel | c.118G>A | p.Ala40Thr | p.A40T | Q03060 | protein_coding | deleterious_low_confidence(0.04) | possibly_damaging(0.769) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CREM | SNV | Missense_Mutation | novel | c.59N>G | p.Glu20Gly | p.E20G | Q03060 | protein_coding | deleterious_low_confidence(0.04) | benign(0.341) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CREM | SNV | Missense_Mutation | novel | c.413C>T | p.Ala138Val | p.A138V | Q03060 | protein_coding | tolerated(0.07) | benign(0.346) | TCGA-DM-A1D8-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
CREM | SNV | Missense_Mutation | c.848N>A | p.Leu283His | p.L283H | Q03060 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-EI-6513-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | SD | |
CREM | SNV | Missense_Mutation | novel | c.186N>T | p.Glu62Asp | p.E62D | Q03060 | protein_coding | tolerated(0.15) | benign(0.358) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
CREM | SNV | Missense_Mutation | novel | c.147T>A | p.Asn49Lys | p.N49K | Q03060 | protein_coding | tolerated(0.2) | benign(0.096) | TCGA-AJ-A23O-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | 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 |
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