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Gene: MEIS3 |
Gene summary for MEIS3 |
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Gene information | Species | Human | Gene symbol | MEIS3 | Gene ID | 56917 |
Gene name | Meis homeobox 3 | |
Gene Alias | MRG2 | |
Cytomap | 19q13.32 | |
Gene Type | protein-coding | GO ID | GO:0001654 | UniProtAcc | A0A024R0S2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
56917 | MEIS3 | C30 | Human | Oral cavity | OSCC | 8.97e-12 | 7.09e-01 | 0.3055 |
56917 | MEIS3 | C38 | Human | Oral cavity | OSCC | 4.26e-06 | 6.18e-01 | 0.172 |
56917 | MEIS3 | C09 | Human | Oral cavity | OSCC | 4.00e-05 | 3.68e-01 | 0.1431 |
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Tissue | Expression Dynamics | Abbreviation |
Oral Cavity | ![]() | EOLP: Erosive Oral lichen planus |
LP: leukoplakia | ||
NEOLP: Non-erosive oral lichen planus | ||
OSCC: Oral squamous cell carcinoma |
∗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:200123320 | Oral cavity | OSCC | regulation of apoptotic signaling pathway | 242/7305 | 356/18723 | 6.66e-29 | 3.24e-26 | 242 |
GO:200123420 | Oral cavity | OSCC | negative regulation of apoptotic signaling pathway | 148/7305 | 224/18723 | 1.71e-16 | 1.36e-14 | 148 |
GO:00434916 | Oral cavity | OSCC | protein kinase B signaling | 103/7305 | 211/18723 | 2.29e-03 | 1.02e-02 | 103 |
GO:00518976 | Oral cavity | OSCC | positive regulation of protein kinase B signaling | 61/7305 | 120/18723 | 5.52e-03 | 2.14e-02 | 61 |
GO:00518967 | Oral cavity | OSCC | regulation of protein kinase B signaling | 88/7305 | 185/18723 | 1.07e-02 | 3.64e-02 | 88 |
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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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∗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 |
MEIS3 | SNV | Missense_Mutation | novel | c.401N>C | p.Ile134Thr | p.I134T | Q99687 | protein_coding | deleterious(0) | benign(0.273) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MEIS3 | SNV | Missense_Mutation | rs754882587 | c.980C>T | p.Ser327Phe | p.S327F | Q99687 | protein_coding | tolerated_low_confidence(0.73) | benign(0.007) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
MEIS3 | SNV | Missense_Mutation | c.1084N>A | p.Ala362Thr | p.A362T | Q99687 | protein_coding | deleterious(0) | possibly_damaging(0.765) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
MEIS3 | SNV | Missense_Mutation | novel | c.1088G>A | p.Arg363Gln | p.R363Q | Q99687 | protein_coding | deleterious(0) | benign(0.288) | TCGA-AA-3949-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
MEIS3 | SNV | Missense_Mutation | rs752747235 | c.781N>T | p.Arg261Trp | p.R261W | Q99687 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-AA-A02W-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
MEIS3 | SNV | Missense_Mutation | c.1201N>A | p.Ala401Thr | p.A401T | Q99687 | protein_coding | tolerated_low_confidence(0.55) | benign(0) | TCGA-AD-6964-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Chemotherapy | folfox | PD | |
MEIS3 | SNV | Missense_Mutation | c.881N>G | p.Leu294Arg | p.L294R | Q99687 | protein_coding | tolerated_low_confidence(0.21) | benign(0.112) | TCGA-AM-5821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MEIS3 | SNV | Missense_Mutation | c.76N>A | p.Glu26Lys | p.E26K | Q99687 | protein_coding | tolerated(0.06) | probably_damaging(0.991) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MEIS3 | SNV | Missense_Mutation | c.338N>T | p.Ala113Val | p.A113V | Q99687 | protein_coding | tolerated(0.24) | possibly_damaging(0.737) | TCGA-CM-5864-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
MEIS3 | SNV | Missense_Mutation | c.1114N>A | p.Asp372Asn | p.D372N | Q99687 | protein_coding | deleterious(0.01) | benign(0.017) | TCGA-F4-6570-01 | 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 |
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