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Gene: MMD |
Gene summary for MMD |
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Gene information | Species | Human | Gene symbol | MMD | Gene ID | 23531 |
Gene name | monocyte to macrophage differentiation associated | |
Gene Alias | MMA | |
Cytomap | 17q22 | |
Gene Type | protein-coding | GO ID | GO:0001932 | UniProtAcc | Q15546 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
23531 | MMD | P2T-E | Human | Esophagus | ESCC | 2.65e-18 | 3.53e-01 | 0.1177 |
23531 | MMD | P4T-E | Human | Esophagus | ESCC | 8.53e-15 | 4.80e-01 | 0.1323 |
23531 | MMD | P8T-E | Human | Esophagus | ESCC | 1.97e-10 | 1.79e-01 | 0.0889 |
23531 | MMD | P9T-E | Human | Esophagus | ESCC | 2.19e-10 | 3.28e-01 | 0.1131 |
23531 | MMD | P10T-E | Human | Esophagus | ESCC | 4.71e-53 | 8.48e-01 | 0.116 |
23531 | MMD | P11T-E | Human | Esophagus | ESCC | 1.92e-04 | 2.66e-01 | 0.1426 |
23531 | MMD | P12T-E | Human | Esophagus | ESCC | 1.75e-25 | 4.92e-01 | 0.1122 |
23531 | MMD | P15T-E | Human | Esophagus | ESCC | 3.42e-03 | 2.56e-01 | 0.1149 |
23531 | MMD | P16T-E | Human | Esophagus | ESCC | 1.96e-11 | 2.45e-01 | 0.1153 |
23531 | MMD | P21T-E | Human | Esophagus | ESCC | 8.08e-19 | 3.85e-01 | 0.1617 |
23531 | MMD | P22T-E | Human | Esophagus | ESCC | 4.24e-18 | 3.19e-01 | 0.1236 |
23531 | MMD | P24T-E | Human | Esophagus | ESCC | 1.26e-02 | 9.15e-02 | 0.1287 |
23531 | MMD | P26T-E | Human | Esophagus | ESCC | 3.19e-23 | 4.29e-01 | 0.1276 |
23531 | MMD | P27T-E | Human | Esophagus | ESCC | 1.60e-10 | 2.40e-01 | 0.1055 |
23531 | MMD | P28T-E | Human | Esophagus | ESCC | 9.53e-09 | 1.51e-01 | 0.1149 |
23531 | MMD | P30T-E | Human | Esophagus | ESCC | 2.02e-07 | 4.88e-01 | 0.137 |
23531 | MMD | P31T-E | Human | Esophagus | ESCC | 7.31e-14 | 2.37e-01 | 0.1251 |
23531 | MMD | P32T-E | Human | Esophagus | ESCC | 1.88e-11 | 2.86e-01 | 0.1666 |
23531 | MMD | P37T-E | Human | Esophagus | ESCC | 5.88e-05 | 2.66e-01 | 0.1371 |
23531 | MMD | P39T-E | Human | Esophagus | ESCC | 2.09e-05 | 6.41e-02 | 0.0894 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00510904 | Cervix | CC | regulation of DNA-binding transcription factor activity | 87/2311 | 440/18723 | 4.85e-06 | 1.22e-04 | 87 |
GO:005109012 | Cervix | HSIL_HPV | regulation of DNA-binding transcription factor activity | 35/737 | 440/18723 | 6.77e-05 | 1.58e-03 | 35 |
GO:0042176 | Colorectum | AD | regulation of protein catabolic process | 160/3918 | 391/18723 | 1.06e-19 | 7.34e-17 | 160 |
GO:1903362 | Colorectum | AD | regulation of cellular protein catabolic process | 109/3918 | 255/18723 | 2.14e-15 | 6.08e-13 | 109 |
GO:0010498 | Colorectum | AD | proteasomal protein catabolic process | 174/3918 | 490/18723 | 3.18e-14 | 7.66e-12 | 174 |
GO:1903050 | Colorectum | AD | regulation of proteolysis involved in cellular protein catabolic process | 92/3918 | 221/18723 | 2.04e-12 | 3.19e-10 | 92 |
GO:0043161 | Colorectum | AD | proteasome-mediated ubiquitin-dependent protein catabolic process | 141/3918 | 412/18723 | 1.77e-10 | 1.68e-08 | 141 |
GO:0048193 | Colorectum | AD | Golgi vesicle transport | 109/3918 | 296/18723 | 1.80e-10 | 1.68e-08 | 109 |
GO:0061136 | Colorectum | AD | regulation of proteasomal protein catabolic process | 75/3918 | 187/18723 | 1.65e-09 | 1.20e-07 | 75 |
GO:2000058 | Colorectum | AD | regulation of ubiquitin-dependent protein catabolic process | 68/3918 | 164/18723 | 1.82e-09 | 1.31e-07 | 68 |
GO:0098876 | Colorectum | AD | vesicle-mediated transport to the plasma membrane | 57/3918 | 136/18723 | 2.30e-08 | 1.27e-06 | 57 |
GO:1903320 | Colorectum | AD | regulation of protein modification by small protein conjugation or removal | 86/3918 | 242/18723 | 9.43e-08 | 4.65e-06 | 86 |
GO:0006892 | Colorectum | AD | post-Golgi vesicle-mediated transport | 45/3918 | 104/18723 | 2.22e-07 | 9.26e-06 | 45 |
GO:0032434 | Colorectum | AD | regulation of proteasomal ubiquitin-dependent protein catabolic process | 54/3918 | 134/18723 | 2.51e-07 | 1.02e-05 | 54 |
GO:0055076 | Colorectum | AD | transition metal ion homeostasis | 53/3918 | 138/18723 | 1.89e-06 | 5.65e-05 | 53 |
GO:0031396 | Colorectum | AD | regulation of protein ubiquitination | 72/3918 | 210/18723 | 4.50e-06 | 1.21e-04 | 72 |
GO:0006893 | Colorectum | AD | Golgi to plasma membrane transport | 27/3918 | 60/18723 | 2.41e-05 | 4.66e-04 | 27 |
GO:0002028 | Colorectum | AD | regulation of sodium ion transport | 36/3918 | 90/18723 | 2.89e-05 | 5.37e-04 | 36 |
GO:1902305 | Colorectum | AD | regulation of sodium ion transmembrane transport | 27/3918 | 68/18723 | 3.19e-04 | 3.80e-03 | 27 |
GO:1903828 | Colorectum | AD | negative regulation of cellular protein localization | 39/3918 | 117/18723 | 1.18e-03 | 1.06e-02 | 39 |
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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 |
MMD | SNV | Missense_Mutation | c.121C>T | p.Pro41Ser | p.P41S | Q15546 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-A7-A0D9-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | SD | |
MMD | SNV | Missense_Mutation | novel | c.605N>T | p.Pro202Leu | p.P202L | Q15546 | protein_coding | deleterious(0.02) | possibly_damaging(0.766) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
MMD | SNV | Missense_Mutation | c.649G>A | p.Ala217Thr | p.A217T | Q15546 | protein_coding | tolerated(0.09) | possibly_damaging(0.543) | TCGA-F4-6570-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MMD | insertion | Frame_Shift_Ins | novel | c.713_714insT | p.Leu238PhefsTer7 | p.L238Ffs*7 | Q15546 | protein_coding | TCGA-AD-6889-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Chemotherapy | xeloda | PD | ||
MMD | SNV | Missense_Mutation | novel | c.134N>A | p.Gly45Asp | p.G45D | Q15546 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MMD | SNV | Missense_Mutation | rs772130160 | c.632N>C | p.Phe211Ser | p.F211S | Q15546 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
MMD | SNV | Missense_Mutation | novel | c.559N>C | p.Ile187Leu | p.I187L | Q15546 | protein_coding | tolerated(0.54) | benign(0) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MMD | SNV | Missense_Mutation | c.355C>T | p.Arg119Cys | p.R119C | Q15546 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD | |
MMD | SNV | Missense_Mutation | rs374125073 | c.223G>A | p.Val75Ile | p.V75I | Q15546 | protein_coding | tolerated(0.07) | benign(0.044) | TCGA-AP-A0LM-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | cisplatin | SD |
MMD | SNV | Missense_Mutation | c.12N>T | p.Lys4Asn | p.K4N | Q15546 | protein_coding | tolerated(0.13) | benign(0) | TCGA-AP-A1DV-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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