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Gene: ADAM12 |
Gene summary for ADAM12 |
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Gene information | Species | Human | Gene symbol | ADAM12 | Gene ID | 8038 |
Gene name | ADAM metallopeptidase domain 12 | |
Gene Alias | ADAM12-OT1 | |
Cytomap | 10q26.2 | |
Gene Type | protein-coding | GO ID | GO:0000768 | UniProtAcc | U5NE98 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
8038 | ADAM12 | PTC06 | Human | Thyroid | PTC | 1.21e-02 | 1.08e-01 | 0.2057 |
8038 | ADAM12 | PTC07 | Human | Thyroid | PTC | 2.29e-02 | 6.69e-02 | 0.2044 |
8038 | ADAM12 | ATC11 | Human | Thyroid | ATC | 7.49e-03 | 4.71e-01 | 0.3386 |
8038 | ADAM12 | ATC12 | Human | Thyroid | ATC | 3.80e-36 | 7.43e-01 | 0.34 |
8038 | ADAM12 | ATC13 | Human | Thyroid | ATC | 7.40e-31 | 6.66e-01 | 0.34 |
8038 | ADAM12 | ATC2 | Human | Thyroid | ATC | 4.44e-15 | 1.27e+00 | 0.34 |
8038 | ADAM12 | ATC3 | Human | Thyroid | ATC | 5.97e-08 | 5.39e-01 | 0.338 |
8038 | ADAM12 | ATC4 | Human | Thyroid | ATC | 6.18e-45 | 9.12e-01 | 0.34 |
8038 | ADAM12 | ATC5 | Human | Thyroid | ATC | 6.03e-40 | 7.33e-01 | 0.34 |
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Tissue | Expression Dynamics | Abbreviation |
Thyroid | ![]() | ATC: Anaplastic thyroid cancer |
HT: Hashimoto's thyroiditis | ||
PTC: Papillary thyroid cancer |
∗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:004576612 | Thyroid | PTC | positive regulation of angiogenesis | 75/5968 | 181/18723 | 4.09e-03 | 1.95e-02 | 75 |
GO:190401812 | Thyroid | PTC | positive regulation of vasculature development | 75/5968 | 181/18723 | 4.09e-03 | 1.95e-02 | 75 |
GO:004269216 | Thyroid | ATC | muscle cell differentiation | 165/6293 | 384/18723 | 7.17e-05 | 5.46e-04 | 165 |
GO:004576621 | Thyroid | ATC | positive regulation of angiogenesis | 82/6293 | 181/18723 | 6.79e-04 | 3.83e-03 | 82 |
GO:190401821 | Thyroid | ATC | positive regulation of vasculature development | 82/6293 | 181/18723 | 6.79e-04 | 3.83e-03 | 82 |
GO:005114617 | Thyroid | ATC | striated muscle cell differentiation | 119/6293 | 283/18723 | 1.74e-03 | 8.70e-03 | 119 |
GO:00457657 | Thyroid | ATC | regulation of angiogenesis | 141/6293 | 342/18723 | 1.80e-03 | 8.85e-03 | 141 |
GO:19013427 | Thyroid | ATC | regulation of vasculature development | 143/6293 | 348/18723 | 1.95e-03 | 9.44e-03 | 143 |
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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 |
ADAM12 | SNV | Missense_Mutation | c.697G>C | p.Asp233His | p.D233H | O43184 | protein_coding | deleterious(0.01) | probably_damaging(1) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
ADAM12 | SNV | Missense_Mutation | c.676G>C | p.Glu226Gln | p.E226Q | O43184 | protein_coding | deleterious(0.05) | probably_damaging(0.936) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
ADAM12 | SNV | Missense_Mutation | rs200657108 | c.674G>A | p.Arg225Gln | p.R225Q | O43184 | protein_coding | tolerated(0.16) | probably_damaging(0.996) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
ADAM12 | SNV | Missense_Mutation | c.608G>T | p.Arg203Ile | p.R203I | O43184 | protein_coding | tolerated(0.07) | benign(0.007) | TCGA-AC-A3W6-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
ADAM12 | SNV | Missense_Mutation | novel | c.110N>A | p.Gly37Glu | p.G37E | O43184 | protein_coding | tolerated_low_confidence(0.24) | benign(0) | TCGA-BH-A0DE-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ADAM12 | SNV | Missense_Mutation | rs745765822 | c.329N>A | p.Arg110Gln | p.R110Q | O43184 | protein_coding | tolerated(0.31) | benign(0.053) | TCGA-BH-A0H7-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | doxorubicin | SD |
ADAM12 | SNV | Missense_Mutation | c.860N>C | p.Leu287Pro | p.L287P | O43184 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BH-A1FN-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
ADAM12 | SNV | Missense_Mutation | c.2328N>A | p.Met776Ile | p.M776I | O43184 | protein_coding | tolerated(0.44) | benign(0) | TCGA-C8-A275-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
ADAM12 | SNV | Missense_Mutation | rs767462610 | c.2003N>A | p.Gly668Glu | p.G668E | O43184 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-D8-A1XG-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
ADAM12 | SNV | Missense_Mutation | novel | c.263N>A | p.Gly88Asp | p.G88D | O43184 | protein_coding | tolerated(0.17) | probably_damaging(0.99) | TCGA-OL-A66P-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | cytoxan | CR |
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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 |
8038 | ADAM12 | NEUTRAL ZINC METALLOPEPTIDASE, PROTEASE, DRUGGABLE GENOME, ENZYME | inhibitor | 178103981 | ILOMASTAT |
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