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Gene: TMEM191B |
Gene summary for TMEM191B |
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Gene information | Species | Human | Gene symbol | TMEM191B | Gene ID | 728229 |
Gene name | transmembrane protein 191B | |
Gene Alias | TMEM191B | |
Cytomap | 22q11.21 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | P0C7N4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
728229 | TMEM191B | C04 | Human | Oral cavity | OSCC | 6.76e-09 | 4.04e-01 | 0.2633 |
728229 | TMEM191B | C21 | Human | Oral cavity | OSCC | 1.03e-16 | 4.90e-01 | 0.2678 |
728229 | TMEM191B | C30 | Human | Oral cavity | OSCC | 2.25e-16 | 6.80e-01 | 0.3055 |
728229 | TMEM191B | C43 | Human | Oral cavity | OSCC | 1.37e-13 | 2.42e-01 | 0.1704 |
728229 | TMEM191B | C46 | Human | Oral cavity | OSCC | 3.38e-07 | 1.90e-01 | 0.1673 |
728229 | TMEM191B | C51 | Human | Oral cavity | OSCC | 6.69e-03 | 2.36e-01 | 0.2674 |
728229 | TMEM191B | C57 | Human | Oral cavity | OSCC | 3.59e-04 | 1.80e-01 | 0.1679 |
728229 | TMEM191B | C06 | Human | Oral cavity | OSCC | 4.85e-04 | 5.20e-01 | 0.2699 |
728229 | TMEM191B | C08 | Human | Oral cavity | OSCC | 1.47e-09 | 1.94e-01 | 0.1919 |
728229 | TMEM191B | C09 | Human | Oral cavity | OSCC | 1.27e-06 | 2.67e-01 | 0.1431 |
728229 | TMEM191B | LN46 | Human | Oral cavity | OSCC | 2.57e-02 | 1.89e-01 | 0.1666 |
728229 | TMEM191B | LP15 | Human | Oral cavity | LP | 2.56e-04 | 7.57e-01 | 0.2174 |
728229 | TMEM191B | SYSMH1 | Human | Oral cavity | OSCC | 5.01e-04 | 1.64e-01 | 0.1127 |
728229 | TMEM191B | SYSMH2 | Human | Oral cavity | OSCC | 1.64e-16 | 4.92e-01 | 0.2326 |
728229 | TMEM191B | SYSMH3 | Human | Oral cavity | OSCC | 1.90e-13 | 3.22e-01 | 0.2442 |
728229 | TMEM191B | SYSMH6 | Human | Oral cavity | OSCC | 4.48e-06 | 1.43e-01 | 0.1275 |
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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 |
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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 |
TMEM191B | SNV | Missense_Mutation | novel | c.305G>A | p.Arg102Gln | p.R102Q | P0C7N4 | protein_coding | deleterious(0.04) | probably_damaging(0.975) | TCGA-EK-A2RO-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
TMEM191B | SNV | Missense_Mutation | novel | c.409N>G | p.Lys137Glu | p.K137E | P0C7N4 | protein_coding | tolerated(0.17) | probably_damaging(0.979) | TCGA-AX-A3G8-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
TMEM191B | SNV | Missense_Mutation | novel | c.377N>C | p.Val126Ala | p.V126A | P0C7N4 | protein_coding | tolerated(1) | possibly_damaging(0.657) | TCGA-BG-A222-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TMEM191B | SNV | Missense_Mutation | novel | c.788C>T | p.Ala263Val | p.A263V | P0C7N4 | protein_coding | deleterious_low_confidence(0.02) | possibly_damaging(0.801) | TCGA-D1-A1NY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Chemotherapy | carboplatin | SD |
TMEM191B | SNV | Missense_Mutation | novel | c.788N>T | p.Ala263Val | p.A263V | P0C7N4 | protein_coding | deleterious_low_confidence(0.02) | possibly_damaging(0.801) | TCGA-EY-A215-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
TMEM191B | insertion | In_Frame_Ins | novel | c.480_481insTAT | p.Tyr160dup | p.Y160dup | P0C7N4 | protein_coding | TCGA-DF-A2KU-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | Unknown | 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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