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Gene: DVL1 |
Gene summary for DVL1 |
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Gene information | Species | Human | Gene symbol | DVL1 | Gene ID | 1855 |
Gene name | dishevelled segment polarity protein 1 | |
Gene Alias | DRS2 | |
Cytomap | 1p36.33 | |
Gene Type | protein-coding | GO ID | GO:0000226 | UniProtAcc | O14640 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
1855 | DVL1 | LZE7T | Human | Esophagus | ESCC | 6.63e-03 | 1.01e-01 | 0.0667 |
1855 | DVL1 | LZE20T | Human | Esophagus | ESCC | 1.62e-04 | 1.24e-01 | 0.0662 |
1855 | DVL1 | LZE24T | Human | Esophagus | ESCC | 9.22e-08 | 1.31e-01 | 0.0596 |
1855 | DVL1 | LZE21T | Human | Esophagus | ESCC | 1.29e-02 | 8.75e-02 | 0.0655 |
1855 | DVL1 | P1T-E | Human | Esophagus | ESCC | 6.15e-09 | 3.04e-01 | 0.0875 |
1855 | DVL1 | P2T-E | Human | Esophagus | ESCC | 6.73e-07 | 1.08e-02 | 0.1177 |
1855 | DVL1 | P4T-E | Human | Esophagus | ESCC | 3.65e-15 | 1.72e-01 | 0.1323 |
1855 | DVL1 | P5T-E | Human | Esophagus | ESCC | 9.88e-08 | 9.93e-02 | 0.1327 |
1855 | DVL1 | P8T-E | Human | Esophagus | ESCC | 3.28e-16 | 3.73e-01 | 0.0889 |
1855 | DVL1 | P9T-E | Human | Esophagus | ESCC | 3.14e-07 | 4.08e-02 | 0.1131 |
1855 | DVL1 | P10T-E | Human | Esophagus | ESCC | 9.40e-14 | 8.76e-02 | 0.116 |
1855 | DVL1 | P11T-E | Human | Esophagus | ESCC | 3.28e-06 | 1.57e-01 | 0.1426 |
1855 | DVL1 | P12T-E | Human | Esophagus | ESCC | 1.69e-02 | -2.70e-02 | 0.1122 |
1855 | DVL1 | P15T-E | Human | Esophagus | ESCC | 4.33e-11 | 1.25e-01 | 0.1149 |
1855 | DVL1 | P16T-E | Human | Esophagus | ESCC | 1.69e-04 | -4.12e-02 | 0.1153 |
1855 | DVL1 | P17T-E | Human | Esophagus | ESCC | 7.08e-05 | 1.74e-01 | 0.1278 |
1855 | DVL1 | P20T-E | Human | Esophagus | ESCC | 5.31e-08 | 7.68e-02 | 0.1124 |
1855 | DVL1 | P21T-E | Human | Esophagus | ESCC | 1.83e-10 | 3.37e-01 | 0.1617 |
1855 | DVL1 | P22T-E | Human | Esophagus | ESCC | 2.81e-07 | -1.02e-03 | 0.1236 |
1855 | DVL1 | P23T-E | Human | Esophagus | ESCC | 6.07e-17 | 1.41e-01 | 0.108 |
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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 |
Esophagus | ESCC | ![]() |
Skin | AK | ![]() |
Skin | SCCIS | ![]() |
Skin | cSCC | ![]() |
Thyroid | HT | ![]() |
∗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:0010498111 | Esophagus | ESCC | proteasomal protein catabolic process | 369/8552 | 490/18723 | 1.13e-41 | 1.80e-38 | 369 |
GO:0043161111 | Esophagus | ESCC | proteasome-mediated ubiquitin-dependent protein catabolic process | 312/8552 | 412/18723 | 3.53e-36 | 4.48e-33 | 312 |
GO:0042176111 | Esophagus | ESCC | regulation of protein catabolic process | 280/8552 | 391/18723 | 8.65e-26 | 2.39e-23 | 280 |
GO:0031647111 | Esophagus | ESCC | regulation of protein stability | 223/8552 | 298/18723 | 5.76e-25 | 1.52e-22 | 223 |
GO:0009896111 | Esophagus | ESCC | positive regulation of catabolic process | 332/8552 | 492/18723 | 4.36e-23 | 9.22e-21 | 332 |
GO:0031331111 | Esophagus | ESCC | positive regulation of cellular catabolic process | 292/8552 | 427/18723 | 8.67e-22 | 1.53e-19 | 292 |
GO:003450418 | Esophagus | ESCC | protein localization to nucleus | 211/8552 | 290/18723 | 4.06e-21 | 6.60e-19 | 211 |
GO:1903362111 | Esophagus | ESCC | regulation of cellular protein catabolic process | 188/8552 | 255/18723 | 5.12e-20 | 6.62e-18 | 188 |
GO:0051098111 | Esophagus | ESCC | regulation of binding | 251/8552 | 363/18723 | 6.73e-20 | 8.46e-18 | 251 |
GO:0045862111 | Esophagus | ESCC | positive regulation of proteolysis | 256/8552 | 372/18723 | 7.88e-20 | 9.43e-18 | 256 |
GO:1903050111 | Esophagus | ESCC | regulation of proteolysis involved in cellular protein catabolic process | 163/8552 | 221/18723 | 1.44e-17 | 1.27e-15 | 163 |
GO:0061136111 | Esophagus | ESCC | regulation of proteasomal protein catabolic process | 142/8552 | 187/18723 | 2.40e-17 | 2.00e-15 | 142 |
GO:0045732111 | Esophagus | ESCC | positive regulation of protein catabolic process | 167/8552 | 231/18723 | 1.47e-16 | 1.14e-14 | 167 |
GO:0032434111 | Esophagus | ESCC | regulation of proteasomal ubiquitin-dependent protein catabolic process | 107/8552 | 134/18723 | 4.06e-16 | 2.93e-14 | 107 |
GO:2000058111 | Esophagus | ESCC | regulation of ubiquitin-dependent protein catabolic process | 125/8552 | 164/18723 | 1.17e-15 | 7.76e-14 | 125 |
GO:0050821111 | Esophagus | ESCC | protein stabilization | 140/8552 | 191/18723 | 6.50e-15 | 3.61e-13 | 140 |
GO:1903364111 | Esophagus | ESCC | positive regulation of cellular protein catabolic process | 117/8552 | 155/18723 | 3.25e-14 | 1.66e-12 | 117 |
GO:1901800110 | Esophagus | ESCC | positive regulation of proteasomal protein catabolic process | 91/8552 | 114/18723 | 6.74e-14 | 3.34e-12 | 91 |
GO:1903052110 | Esophagus | ESCC | positive regulation of proteolysis involved in cellular protein catabolic process | 101/8552 | 133/18723 | 9.58e-13 | 4.19e-11 | 101 |
GO:0010563111 | Esophagus | ESCC | negative regulation of phosphorus metabolic process | 274/8552 | 442/18723 | 2.32e-12 | 9.41e-11 | 274 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa05022210 | Esophagus | ESCC | Pathways of neurodegeneration - multiple diseases | 318/4205 | 476/8465 | 6.10e-15 | 2.04e-13 | 1.05e-13 | 318 |
hsa05010210 | Esophagus | ESCC | Alzheimer disease | 263/4205 | 384/8465 | 1.80e-14 | 5.47e-13 | 2.80e-13 | 263 |
hsa0516510 | Esophagus | ESCC | Human papillomavirus infection | 215/4205 | 331/8465 | 7.86e-09 | 7.12e-08 | 3.65e-08 | 215 |
hsa0522518 | Esophagus | ESCC | Hepatocellular carcinoma | 109/4205 | 168/8465 | 4.27e-05 | 1.88e-04 | 9.64e-05 | 109 |
hsa041505 | Esophagus | ESCC | mTOR signaling pathway | 98/4205 | 156/8465 | 5.81e-04 | 1.95e-03 | 9.97e-04 | 98 |
hsa043306 | Esophagus | ESCC | Notch signaling pathway | 42/4205 | 62/8465 | 2.97e-03 | 7.97e-03 | 4.08e-03 | 42 |
hsa0439018 | Esophagus | ESCC | Hippo signaling pathway | 92/4205 | 157/8465 | 1.46e-02 | 3.31e-02 | 1.69e-02 | 92 |
hsa0502238 | Esophagus | ESCC | Pathways of neurodegeneration - multiple diseases | 318/4205 | 476/8465 | 6.10e-15 | 2.04e-13 | 1.05e-13 | 318 |
hsa0501038 | Esophagus | ESCC | Alzheimer disease | 263/4205 | 384/8465 | 1.80e-14 | 5.47e-13 | 2.80e-13 | 263 |
hsa0516515 | Esophagus | ESCC | Human papillomavirus infection | 215/4205 | 331/8465 | 7.86e-09 | 7.12e-08 | 3.65e-08 | 215 |
hsa0522519 | Esophagus | ESCC | Hepatocellular carcinoma | 109/4205 | 168/8465 | 4.27e-05 | 1.88e-04 | 9.64e-05 | 109 |
hsa0415013 | Esophagus | ESCC | mTOR signaling pathway | 98/4205 | 156/8465 | 5.81e-04 | 1.95e-03 | 9.97e-04 | 98 |
hsa0433013 | Esophagus | ESCC | Notch signaling pathway | 42/4205 | 62/8465 | 2.97e-03 | 7.97e-03 | 4.08e-03 | 42 |
hsa0439019 | Esophagus | ESCC | Hippo signaling pathway | 92/4205 | 157/8465 | 1.46e-02 | 3.31e-02 | 1.69e-02 | 92 |
hsa0501022 | Liver | HCC | Alzheimer disease | 254/4020 | 384/8465 | 3.75e-14 | 8.97e-13 | 4.99e-13 | 254 |
hsa0502222 | Liver | HCC | Pathways of neurodegeneration - multiple diseases | 298/4020 | 476/8465 | 6.59e-12 | 1.30e-10 | 7.22e-11 | 298 |
hsa052258 | Liver | HCC | Hepatocellular carcinoma | 106/4020 | 168/8465 | 2.87e-05 | 1.85e-04 | 1.03e-04 | 106 |
hsa051652 | Liver | HCC | Human papillomavirus infection | 188/4020 | 331/8465 | 3.34e-04 | 1.49e-03 | 8.29e-04 | 188 |
hsa041502 | Liver | HCC | mTOR signaling pathway | 95/4020 | 156/8465 | 4.70e-04 | 1.99e-03 | 1.11e-03 | 95 |
hsa0501032 | Liver | HCC | Alzheimer disease | 254/4020 | 384/8465 | 3.75e-14 | 8.97e-13 | 4.99e-13 | 254 |
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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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TF | Cell Type | Tissue | Disease Stage | Target Gene | RSS | Regulon Activity |
∗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 |
DVL1 | SNV | Missense_Mutation | c.1625N>T | p.Tyr542Phe | p.Y542F | O14640 | protein_coding | tolerated(0.11) | possibly_damaging(0.596) | TCGA-A7-A0DA-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | |
DVL1 | SNV | Missense_Mutation | rs766988615 | c.817N>T | p.Arg273Cys | p.R273C | O14640 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-BH-A18T-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
DVL1 | SNV | Missense_Mutation | novel | c.586G>A | p.Glu196Lys | p.E196K | O14640 | protein_coding | deleterious(0.01) | possibly_damaging(0.593) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
DVL1 | SNV | Missense_Mutation | novel | c.1345N>A | p.Asp449Asn | p.D449N | O14640 | protein_coding | deleterious(0.05) | probably_damaging(0.978) | TCGA-EA-A43B-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
DVL1 | SNV | Missense_Mutation | rs766432002 | c.1324N>A | p.Ala442Thr | p.A442T | O14640 | protein_coding | deleterious(0) | possibly_damaging(0.863) | TCGA-5M-AAT6-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
DVL1 | SNV | Missense_Mutation | novel | c.595N>G | p.Ser199Gly | p.S199G | O14640 | protein_coding | tolerated(0.29) | benign(0.01) | TCGA-A6-3809-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
DVL1 | SNV | Missense_Mutation | c.1061C>T | p.Pro354Leu | p.P354L | O14640 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD | |
DVL1 | SNV | Missense_Mutation | novel | c.17T>A | p.Ile6Asn | p.I6N | O14640 | protein_coding | deleterious(0) | possibly_damaging(0.659) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
DVL1 | SNV | Missense_Mutation | rs376597258 | c.857G>A | p.Gly286Asp | p.G286D | O14640 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-CM-4746-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
DVL1 | SNV | Missense_Mutation | c.1130A>G | p.Tyr377Cys | p.Y377C | O14640 | protein_coding | deleterious(0.01) | probably_damaging(0.949) | TCGA-CM-5861-01 | 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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