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Gene: ADAM8 |
Gene summary for ADAM8 |
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Gene information | Species | Human | Gene symbol | ADAM8 | Gene ID | 101 |
Gene name | ADAM metallopeptidase domain 8 | |
Gene Alias | CD156 | |
Cytomap | 10q26.3 | |
Gene Type | protein-coding | GO ID | GO:0000165 | UniProtAcc | P78325 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
101 | ADAM8 | P2T-E | Human | Esophagus | ESCC | 2.62e-04 | 1.44e-01 | 0.1177 |
101 | ADAM8 | P8T-E | Human | Esophagus | ESCC | 2.11e-03 | 1.57e-01 | 0.0889 |
101 | ADAM8 | P21T-E | Human | Esophagus | ESCC | 2.20e-04 | 1.50e-01 | 0.1617 |
101 | ADAM8 | P37T-E | Human | Esophagus | ESCC | 2.20e-02 | 1.33e-01 | 0.1371 |
101 | ADAM8 | P52T-E | Human | Esophagus | ESCC | 2.92e-02 | 1.24e-01 | 0.1555 |
101 | ADAM8 | P62T-E | Human | Esophagus | ESCC | 1.87e-05 | 2.35e-01 | 0.1302 |
101 | ADAM8 | P65T-E | Human | Esophagus | ESCC | 2.80e-02 | 1.10e-01 | 0.0978 |
101 | ADAM8 | P75T-E | Human | Esophagus | ESCC | 2.70e-09 | 1.96e-01 | 0.1125 |
101 | ADAM8 | P76T-E | Human | Esophagus | ESCC | 1.34e-11 | 1.86e-01 | 0.1207 |
101 | ADAM8 | P82T-E | Human | Esophagus | ESCC | 6.99e-05 | 3.37e-01 | 0.1072 |
101 | ADAM8 | P89T-E | Human | Esophagus | ESCC | 4.31e-04 | 7.74e-01 | 0.1752 |
101 | ADAM8 | P91T-E | Human | Esophagus | ESCC | 5.86e-08 | 1.03e+00 | 0.1828 |
101 | ADAM8 | P126T-E | Human | Esophagus | ESCC | 3.09e-02 | 4.91e-01 | 0.1125 |
101 | ADAM8 | P130T-E | Human | Esophagus | ESCC | 3.08e-28 | 6.12e-01 | 0.1676 |
101 | ADAM8 | C04 | Human | Oral cavity | OSCC | 2.16e-05 | 3.87e-01 | 0.2633 |
101 | ADAM8 | C21 | Human | Oral cavity | OSCC | 1.09e-30 | 1.21e+00 | 0.2678 |
101 | ADAM8 | C30 | Human | Oral cavity | OSCC | 1.39e-10 | 6.27e-01 | 0.3055 |
101 | ADAM8 | C38 | Human | Oral cavity | OSCC | 9.97e-03 | 2.88e-01 | 0.172 |
101 | ADAM8 | C43 | Human | Oral cavity | OSCC | 1.30e-20 | 4.56e-01 | 0.1704 |
101 | ADAM8 | C46 | Human | Oral cavity | OSCC | 1.37e-18 | 4.28e-01 | 0.1673 |
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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:00434055 | Esophagus | ESCC | regulation of MAP kinase activity | 102/8552 | 177/18723 | 8.89e-04 | 4.55e-03 | 102 |
GO:004211018 | Esophagus | ESCC | T cell activation | 256/8552 | 487/18723 | 1.18e-03 | 5.87e-03 | 256 |
GO:19031317 | Esophagus | ESCC | mononuclear cell differentiation | 226/8552 | 426/18723 | 1.20e-03 | 5.88e-03 | 226 |
GO:00702271 | Esophagus | ESCC | lymphocyte apoptotic process | 46/8552 | 72/18723 | 1.39e-03 | 6.62e-03 | 46 |
GO:002240919 | Esophagus | ESCC | positive regulation of cell-cell adhesion | 155/8552 | 284/18723 | 1.50e-03 | 7.06e-03 | 155 |
GO:190210510 | Esophagus | ESCC | regulation of leukocyte differentiation | 152/8552 | 279/18723 | 1.82e-03 | 8.35e-03 | 152 |
GO:000181916 | Esophagus | ESCC | positive regulation of cytokine production | 244/8552 | 467/18723 | 2.29e-03 | 1.01e-02 | 244 |
GO:000930617 | Esophagus | ESCC | protein secretion | 190/8552 | 359/18723 | 3.22e-03 | 1.34e-02 | 190 |
GO:190121516 | Esophagus | ESCC | negative regulation of neuron death | 115/8552 | 208/18723 | 3.24e-03 | 1.34e-02 | 115 |
GO:003559217 | Esophagus | ESCC | establishment of protein localization to extracellular region | 190/8552 | 360/18723 | 3.77e-03 | 1.53e-02 | 190 |
GO:00702421 | Esophagus | ESCC | thymocyte apoptotic process | 13/8552 | 16/18723 | 4.05e-03 | 1.62e-02 | 13 |
GO:007169210 | Esophagus | ESCC | protein localization to extracellular region | 193/8552 | 368/18723 | 5.01e-03 | 1.92e-02 | 193 |
GO:00456213 | Esophagus | ESCC | positive regulation of lymphocyte differentiation | 61/8552 | 104/18723 | 5.22e-03 | 1.97e-02 | 61 |
GO:00069294 | Esophagus | ESCC | substrate-dependent cell migration | 17/8552 | 23/18723 | 5.73e-03 | 2.13e-02 | 17 |
GO:00226172 | Esophagus | ESCC | extracellular matrix disassembly | 39/8552 | 63/18723 | 6.92e-03 | 2.52e-02 | 39 |
GO:005087015 | Esophagus | ESCC | positive regulation of T cell activation | 117/8552 | 216/18723 | 7.23e-03 | 2.62e-02 | 117 |
GO:000268515 | Esophagus | ESCC | regulation of leukocyte migration | 114/8552 | 210/18723 | 7.26e-03 | 2.63e-02 | 114 |
GO:00302176 | Esophagus | ESCC | T cell differentiation | 137/8552 | 257/18723 | 8.09e-03 | 2.87e-02 | 137 |
GO:190303916 | Esophagus | ESCC | positive regulation of leukocyte cell-cell adhesion | 128/8552 | 239/18723 | 8.40e-03 | 2.96e-02 | 128 |
GO:005070810 | Esophagus | ESCC | regulation of protein secretion | 142/8552 | 268/18723 | 9.31e-03 | 3.24e-02 | 142 |
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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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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 |
ADAM8 | SNV | Missense_Mutation | novel | c.1003N>C | p.Glu335Gln | p.E335Q | P78325 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-A2-A0CL-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cytoxan | SD |
ADAM8 | SNV | Missense_Mutation | rs761100437 | c.1441N>A | p.Gly481Ser | p.G481S | P78325 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-EW-A1IZ-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | taxotere | SD |
ADAM8 | SNV | Missense_Mutation | rs764039221 | c.2051G>A | p.Arg684His | p.R684H | P78325 | protein_coding | tolerated(0.2) | benign(0.018) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
ADAM8 | SNV | Missense_Mutation | rs375767499 | c.1910C>T | p.Pro637Leu | p.P637L | P78325 | protein_coding | deleterious(0.01) | benign(0.329) | TCGA-DS-A5RQ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Chemotherapy | cisplatin | CR |
ADAM8 | SNV | Missense_Mutation | novel | c.650N>A | p.Gly217Glu | p.G217E | P78325 | protein_coding | deleterious(0.02) | probably_damaging(0.978) | TCGA-VS-A8EJ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | PD |
ADAM8 | SNV | Missense_Mutation | novel | c.235N>G | p.Leu79Val | p.L79V | P78325 | protein_coding | tolerated(0.43) | benign(0.075) | TCGA-A6-5665-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
ADAM8 | SNV | Missense_Mutation | novel | c.242N>T | p.Ser81Phe | p.S81F | P78325 | protein_coding | deleterious(0) | possibly_damaging(0.892) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
ADAM8 | SNV | Missense_Mutation | novel | c.2048N>A | p.Ser683Asn | p.S683N | P78325 | protein_coding | tolerated(0.42) | benign(0.011) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
ADAM8 | SNV | Missense_Mutation | novel | c.1424T>C | p.Leu475Pro | p.L475P | P78325 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-AD-5900-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
ADAM8 | SNV | Missense_Mutation | novel | c.2402N>T | p.Ala801Val | p.A801V | P78325 | protein_coding | tolerated(0.3) | benign(0.046) | TCGA-AD-A5EJ-01 | Colorectum | colon adenocarcinoma | 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 |
101 | ADAM8 | ENZYME, NEUTRAL ZINC METALLOPEPTIDASE, CELL SURFACE, DRUGGABLE GENOME, PROTEASE | inhibitor | 252166879 |
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