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Gene: MLX |
Gene summary for MLX |
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Gene information | Species | Human | Gene symbol | MLX | Gene ID | 6945 |
Gene name | MAX dimerization protein MLX | |
Gene Alias | MAD7 | |
Cytomap | 17q21.2 | |
Gene Type | protein-coding | GO ID | GO:0000122 | UniProtAcc | Q9UH92 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
6945 | MLX | P19T-E | Human | Esophagus | ESCC | 2.69e-11 | 1.17e+00 | 0.1662 |
6945 | MLX | P20T-E | Human | Esophagus | ESCC | 2.10e-42 | 7.83e-01 | 0.1124 |
6945 | MLX | P21T-E | Human | Esophagus | ESCC | 3.09e-54 | 1.16e+00 | 0.1617 |
6945 | MLX | P22T-E | Human | Esophagus | ESCC | 1.24e-29 | 5.64e-01 | 0.1236 |
6945 | MLX | P23T-E | Human | Esophagus | ESCC | 4.59e-48 | 1.10e+00 | 0.108 |
6945 | MLX | P24T-E | Human | Esophagus | ESCC | 2.21e-28 | 6.20e-01 | 0.1287 |
6945 | MLX | P26T-E | Human | Esophagus | ESCC | 2.70e-28 | 4.62e-01 | 0.1276 |
6945 | MLX | P27T-E | Human | Esophagus | ESCC | 1.06e-30 | 6.61e-01 | 0.1055 |
6945 | MLX | P28T-E | Human | Esophagus | ESCC | 3.98e-28 | 6.72e-01 | 0.1149 |
6945 | MLX | P30T-E | Human | Esophagus | ESCC | 3.30e-28 | 9.20e-01 | 0.137 |
6945 | MLX | P31T-E | Human | Esophagus | ESCC | 9.44e-29 | 5.70e-01 | 0.1251 |
6945 | MLX | P32T-E | Human | Esophagus | ESCC | 9.87e-58 | 1.20e+00 | 0.1666 |
6945 | MLX | P36T-E | Human | Esophagus | ESCC | 1.47e-31 | 9.07e-01 | 0.1187 |
6945 | MLX | P37T-E | Human | Esophagus | ESCC | 4.13e-35 | 7.48e-01 | 0.1371 |
6945 | MLX | P38T-E | Human | Esophagus | ESCC | 1.16e-09 | 5.30e-01 | 0.127 |
6945 | MLX | P39T-E | Human | Esophagus | ESCC | 4.45e-22 | 3.28e-01 | 0.0894 |
6945 | MLX | P40T-E | Human | Esophagus | ESCC | 1.97e-11 | 3.23e-01 | 0.109 |
6945 | MLX | P42T-E | Human | Esophagus | ESCC | 5.76e-25 | 7.35e-01 | 0.1175 |
6945 | MLX | P44T-E | Human | Esophagus | ESCC | 1.39e-11 | 3.55e-01 | 0.1096 |
6945 | MLX | P47T-E | Human | Esophagus | ESCC | 3.77e-17 | 3.62e-01 | 0.1067 |
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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:0046034 | Colorectum | AD | ATP metabolic process | 142/3918 | 277/18723 | 2.64e-29 | 8.26e-26 | 142 |
GO:0006091 | Colorectum | AD | generation of precursor metabolites and energy | 209/3918 | 490/18723 | 3.17e-28 | 6.61e-25 | 209 |
GO:0009060 | Colorectum | AD | aerobic respiration | 108/3918 | 189/18723 | 9.14e-28 | 1.43e-24 | 108 |
GO:0045333 | Colorectum | AD | cellular respiration | 119/3918 | 230/18723 | 3.21e-25 | 4.02e-22 | 119 |
GO:0006119 | Colorectum | AD | oxidative phosphorylation | 83/3918 | 141/18723 | 7.95e-23 | 8.30e-20 | 83 |
GO:0015980 | Colorectum | AD | energy derivation by oxidation of organic compounds | 143/3918 | 318/18723 | 2.78e-22 | 2.49e-19 | 143 |
GO:0009896 | Colorectum | AD | positive regulation of catabolic process | 180/3918 | 492/18723 | 4.33e-16 | 1.94e-13 | 180 |
GO:0009150 | Colorectum | AD | purine ribonucleotide metabolic process | 142/3918 | 368/18723 | 4.29e-15 | 1.17e-12 | 142 |
GO:0006163 | Colorectum | AD | purine nucleotide metabolic process | 149/3918 | 396/18723 | 1.08e-14 | 2.80e-12 | 149 |
GO:0072521 | Colorectum | AD | purine-containing compound metabolic process | 153/3918 | 416/18723 | 4.34e-14 | 1.01e-11 | 153 |
GO:0031331 | Colorectum | AD | positive regulation of cellular catabolic process | 156/3918 | 427/18723 | 4.68e-14 | 1.05e-11 | 156 |
GO:0009259 | Colorectum | AD | ribonucleotide metabolic process | 144/3918 | 385/18723 | 5.25e-14 | 1.13e-11 | 144 |
GO:0019693 | Colorectum | AD | ribose phosphate metabolic process | 145/3918 | 396/18723 | 3.01e-13 | 5.71e-11 | 145 |
GO:0009117 | Colorectum | AD | nucleotide metabolic process | 168/3918 | 489/18723 | 2.20e-12 | 3.36e-10 | 168 |
GO:0006753 | Colorectum | AD | nucleoside phosphate metabolic process | 169/3918 | 497/18723 | 4.99e-12 | 6.98e-10 | 169 |
GO:0009135 | Colorectum | AD | purine nucleoside diphosphate metabolic process | 47/3918 | 103/18723 | 1.61e-08 | 9.22e-07 | 47 |
GO:0009179 | Colorectum | AD | purine ribonucleoside diphosphate metabolic process | 47/3918 | 103/18723 | 1.61e-08 | 9.22e-07 | 47 |
GO:0006090 | Colorectum | AD | pyruvate metabolic process | 47/3918 | 106/18723 | 4.85e-08 | 2.55e-06 | 47 |
GO:0009185 | Colorectum | AD | ribonucleoside diphosphate metabolic process | 47/3918 | 106/18723 | 4.85e-08 | 2.55e-06 | 47 |
GO:0046031 | Colorectum | AD | ADP metabolic process | 41/3918 | 90/18723 | 1.37e-07 | 6.42e-06 | 41 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa04932210 | Esophagus | ESCC | Non-alcoholic fatty liver disease | 122/4205 | 155/8465 | 5.69e-14 | 1.59e-12 | 8.14e-13 | 122 |
hsa049318 | Esophagus | ESCC | Insulin resistance | 69/4205 | 108/8465 | 1.92e-03 | 5.54e-03 | 2.84e-03 | 69 |
hsa0493238 | Esophagus | ESCC | Non-alcoholic fatty liver disease | 122/4205 | 155/8465 | 5.69e-14 | 1.59e-12 | 8.14e-13 | 122 |
hsa0493113 | Esophagus | ESCC | Insulin resistance | 69/4205 | 108/8465 | 1.92e-03 | 5.54e-03 | 2.84e-03 | 69 |
hsa0493222 | Liver | Cirrhotic | Non-alcoholic fatty liver disease | 106/2530 | 155/8465 | 2.16e-23 | 2.40e-21 | 1.48e-21 | 106 |
hsa0493232 | Liver | Cirrhotic | Non-alcoholic fatty liver disease | 106/2530 | 155/8465 | 2.16e-23 | 2.40e-21 | 1.48e-21 | 106 |
hsa0493242 | Liver | HCC | Non-alcoholic fatty liver disease | 124/4020 | 155/8465 | 4.54e-17 | 2.54e-15 | 1.41e-15 | 124 |
hsa0493121 | Liver | HCC | Insulin resistance | 77/4020 | 108/8465 | 3.89e-07 | 4.46e-06 | 2.48e-06 | 77 |
hsa0493252 | Liver | HCC | Non-alcoholic fatty liver disease | 124/4020 | 155/8465 | 4.54e-17 | 2.54e-15 | 1.41e-15 | 124 |
hsa0493131 | Liver | HCC | Insulin resistance | 77/4020 | 108/8465 | 3.89e-07 | 4.46e-06 | 2.48e-06 | 77 |
hsa0493228 | Oral cavity | OSCC | Non-alcoholic fatty liver disease | 124/3704 | 155/8465 | 1.22e-20 | 1.37e-18 | 6.96e-19 | 124 |
hsa049317 | Oral cavity | OSCC | Insulin resistance | 60/3704 | 108/8465 | 8.66e-03 | 1.97e-02 | 1.00e-02 | 60 |
hsa04932112 | Oral cavity | OSCC | Non-alcoholic fatty liver disease | 124/3704 | 155/8465 | 1.22e-20 | 1.37e-18 | 6.96e-19 | 124 |
hsa0493112 | Oral cavity | OSCC | Insulin resistance | 60/3704 | 108/8465 | 8.66e-03 | 1.97e-02 | 1.00e-02 | 60 |
hsa0493229 | Oral cavity | LP | Non-alcoholic fatty liver disease | 101/2418 | 155/8465 | 1.53e-21 | 6.37e-20 | 4.10e-20 | 101 |
hsa0493237 | Oral cavity | LP | Non-alcoholic fatty liver disease | 101/2418 | 155/8465 | 1.53e-21 | 6.37e-20 | 4.10e-20 | 101 |
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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 |
MLX | SNV | Missense_Mutation | novel | c.773N>T | p.Ser258Leu | p.S258L | Q9UH92 | protein_coding | deleterious(0) | benign(0.358) | TCGA-BH-A2L8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | CR |
MLX | SNV | Missense_Mutation | c.350N>T | p.Tyr117Phe | p.Y117F | Q9UH92 | protein_coding | tolerated(0.29) | benign(0.438) | TCGA-E2-A1LS-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Cyclophosphamide | SD | |
MLX | SNV | Missense_Mutation | c.703G>C | p.Asp235His | p.D235H | Q9UH92 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-E9-A1R4-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | 5-fluorouracil | SD | |
MLX | insertion | Frame_Shift_Ins | novel | c.813_814insACCCTAGGGGG | p.Trp272ThrfsTer19 | p.W272Tfs*19 | Q9UH92 | protein_coding | TCGA-BH-A0B8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | arimidex | SD | ||
MLX | SNV | Missense_Mutation | c.520N>A | p.Ala174Thr | p.A174T | Q9UH92 | protein_coding | deleterious(0.03) | probably_damaging(0.948) | TCGA-FU-A3HZ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
MLX | SNV | Missense_Mutation | rs759737992 | c.430G>A | p.Ala144Thr | p.A144T | Q9UH92 | protein_coding | deleterious(0.01) | possibly_damaging(0.835) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
MLX | SNV | Missense_Mutation | c.800C>T | p.Ala267Val | p.A267V | Q9UH92 | protein_coding | deleterious(0.04) | possibly_damaging(0.709) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
MLX | SNV | Missense_Mutation | c.433A>T | p.Ile145Phe | p.I145F | Q9UH92 | protein_coding | deleterious(0) | possibly_damaging(0.904) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MLX | SNV | Missense_Mutation | rs759737992 | c.430N>A | p.Ala144Thr | p.A144T | Q9UH92 | protein_coding | deleterious(0.01) | possibly_damaging(0.835) | TCGA-DC-4749-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
MLX | SNV | Missense_Mutation | novel | c.304N>G | p.Thr102Ala | p.T102A | Q9UH92 | protein_coding | deleterious(0.01) | benign(0.057) | TCGA-A5-A0G1-01 | 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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