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Gene: MS4A1 |
Gene summary for MS4A1 |
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Gene information | Species | Human | Gene symbol | MS4A1 | Gene ID | 931 |
Gene name | membrane spanning 4-domains A1 | |
Gene Alias | B1 | |
Cytomap | 11q12.2 | |
Gene Type | protein-coding | GO ID | GO:0001775 | UniProtAcc | A0A024R507 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
931 | MS4A1 | Adj_PTCwithHT_6 | Human | Thyroid | HT | 3.72e-25 | 1.03e+00 | 0.02 |
931 | MS4A1 | PTCwithHT_6 | Human | Thyroid | HT | 1.77e-07 | 5.12e-01 | 0.02 |
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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:007066110 | Thyroid | HT | leukocyte proliferation | 44/1272 | 318/18723 | 5.29e-06 | 1.64e-04 | 44 |
GO:19031319 | Thyroid | HT | mononuclear cell differentiation | 54/1272 | 426/18723 | 6.88e-06 | 2.00e-04 | 54 |
GO:00466519 | Thyroid | HT | lymphocyte proliferation | 40/1272 | 288/18723 | 1.27e-05 | 3.30e-04 | 40 |
GO:00329438 | Thyroid | HT | mononuclear cell proliferation | 40/1272 | 291/18723 | 1.63e-05 | 3.95e-04 | 40 |
GO:00300986 | Thyroid | HT | lymphocyte differentiation | 47/1272 | 374/18723 | 3.32e-05 | 7.02e-04 | 47 |
GO:00022536 | Thyroid | HT | activation of immune response | 47/1272 | 375/18723 | 3.55e-05 | 7.40e-04 | 47 |
GO:00069598 | Thyroid | HT | humoral immune response | 40/1272 | 317/18723 | 1.14e-04 | 1.86e-03 | 40 |
GO:00421133 | Thyroid | HT | B cell activation | 39/1272 | 334/18723 | 6.66e-04 | 7.61e-03 | 39 |
GO:00027648 | Thyroid | HT | immune response-regulating signaling pathway | 50/1272 | 468/18723 | 9.96e-04 | 1.02e-02 | 50 |
GO:00508515 | Thyroid | HT | antigen receptor-mediated signaling pathway | 27/1272 | 240/18723 | 6.87e-03 | 4.20e-02 | 27 |
GO:00024293 | Thyroid | HT | immune response-activating cell surface receptor signaling pathway | 31/1272 | 291/18723 | 8.69e-03 | 4.92e-02 | 31 |
GO:00027573 | Thyroid | HT | immune response-activating signal transduction | 31/1272 | 291/18723 | 8.69e-03 | 4.92e-02 | 31 |
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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 |
MS4A1 | SNV | Missense_Mutation | c.74N>G | p.Ser25Cys | p.S25C | P11836 | protein_coding | deleterious(0.02) | benign(0.006) | TCGA-BH-A209-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MS4A1 | SNV | Missense_Mutation | c.573N>T | p.Leu191Phe | p.L191F | P11836 | protein_coding | deleterious(0.02) | probably_damaging(0.999) | TCGA-EW-A1P7-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | PD | |
MS4A1 | insertion | In_Frame_Ins | novel | c.582_583insGTTGTTACTGTTGTTGCT | p.Leu194_Ser195insValValThrValValAla | p.L194_S195insVVTVVA | P11836 | protein_coding | TCGA-AN-A0FS-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
MS4A1 | insertion | Frame_Shift_Ins | novel | c.584_585insTGCTTTTTTTATTTCCATTT | p.Val196AlafsTer7 | p.V196Afs*7 | P11836 | protein_coding | TCGA-AN-A0FS-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
MS4A1 | insertion | Frame_Shift_Ins | novel | c.55_56insGATCTGACTCAGGAGGCCACAGTCTTATATACTGCATTAGAAA | p.Pro20SerfsTer45 | p.P20Sfs*45 | P11836 | protein_coding | TCGA-BH-A0HK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | ||
MS4A1 | SNV | Missense_Mutation | rs748214132 | c.751G>A | p.Glu251Lys | p.E251K | P11836 | protein_coding | tolerated(0.17) | benign(0.202) | TCGA-C5-A3HE-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | PD |
MS4A1 | SNV | Missense_Mutation | c.771N>T | p.Lys257Asn | p.K257N | P11836 | protein_coding | deleterious(0.05) | probably_damaging(0.991) | TCGA-AA-3712-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
MS4A1 | SNV | Missense_Mutation | rs188842906 | c.656C>T | p.Thr219Met | p.T219M | P11836 | protein_coding | tolerated(0.57) | benign(0) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
MS4A1 | SNV | Missense_Mutation | c.625N>A | p.Ala209Thr | p.A209T | P11836 | protein_coding | deleterious(0.03) | possibly_damaging(0.795) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
MS4A1 | SNV | Missense_Mutation | novel | c.429N>G | p.Ile143Met | p.I143M | P11836 | protein_coding | tolerated(0.1) | benign(0.021) | TCGA-CA-6717-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | 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 |
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | Anti-CD19/20-CAR vector-transduced T cells | |||
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | inhibitor | CHEMBL1201604 | TOSITUMOMAB | |
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | Rituxan Hemotalogy/oncology | |||
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | antibody | RITUXIMAB | RITUXIMAB | |
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | Rituximab | RITUXIMAB | ||
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | antibody | 363894127 | ||
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | inhibitor | CHEMBL1743088 | VELTUZUMAB | |
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | antibody | 252166480 | VELTUZUMAB | |
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | SBI-087 | 19604259 | ||
931 | MS4A1 | CLINICALLY ACTIONABLE, EXTERNAL SIDE OF PLASMA MEMBRANE, CELL SURFACE, DRUGGABLE GENOME | antibody | 310264701 | UBLITUXIMAB |
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