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Gene: MTMR11 |
Gene summary for MTMR11 |
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Gene information | Species | Human | Gene symbol | MTMR11 | Gene ID | 10903 |
Gene name | myotubularin related protein 11 | |
Gene Alias | CRA | |
Cytomap | 1q21.2 | |
Gene Type | protein-coding | GO ID | GO:0006629 | UniProtAcc | A4FU01 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10903 | MTMR11 | HTA11_2487_2000001011 | Human | Colorectum | SER | 1.72e-08 | 4.47e-01 | -0.1808 |
10903 | MTMR11 | HTA11_1938_2000001011 | Human | Colorectum | AD | 7.58e-16 | 8.94e-01 | -0.0811 |
10903 | MTMR11 | HTA11_78_2000001011 | Human | Colorectum | AD | 4.23e-06 | 5.00e-01 | -0.1088 |
10903 | MTMR11 | HTA11_347_2000001011 | Human | Colorectum | AD | 8.23e-12 | 5.28e-01 | -0.1954 |
10903 | MTMR11 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 1.57e-03 | 2.97e-01 | 0.3859 |
10903 | MTMR11 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 1.50e-02 | -2.14e-01 | 0.3005 |
10903 | MTMR11 | A015-C-203 | Human | Colorectum | FAP | 2.64e-05 | -2.07e-01 | -0.1294 |
10903 | MTMR11 | A015-C-104 | Human | Colorectum | FAP | 8.56e-03 | -1.68e-01 | -0.1899 |
10903 | MTMR11 | A002-C-116 | Human | Colorectum | FAP | 4.34e-03 | -1.23e-01 | -0.0452 |
10903 | MTMR11 | F072B | Human | Colorectum | FAP | 1.25e-02 | -1.38e-01 | 0.257 |
10903 | MTMR11 | LZE6T | Human | Esophagus | ESCC | 1.40e-03 | 3.31e-01 | 0.0845 |
10903 | MTMR11 | P2T-E | Human | Esophagus | ESCC | 5.47e-10 | 2.00e-01 | 0.1177 |
10903 | MTMR11 | P5T-E | Human | Esophagus | ESCC | 2.70e-05 | 7.36e-02 | 0.1327 |
10903 | MTMR11 | P10T-E | Human | Esophagus | ESCC | 6.55e-11 | 5.19e-02 | 0.116 |
10903 | MTMR11 | P12T-E | Human | Esophagus | ESCC | 5.10e-04 | 6.02e-02 | 0.1122 |
10903 | MTMR11 | P16T-E | Human | Esophagus | ESCC | 2.17e-06 | 1.12e-01 | 0.1153 |
10903 | MTMR11 | P19T-E | Human | Esophagus | ESCC | 9.53e-05 | 3.22e-01 | 0.1662 |
10903 | MTMR11 | P21T-E | Human | Esophagus | ESCC | 1.29e-02 | 8.26e-02 | 0.1617 |
10903 | MTMR11 | P22T-E | Human | Esophagus | ESCC | 3.68e-02 | 5.30e-02 | 0.1236 |
10903 | MTMR11 | P24T-E | Human | Esophagus | ESCC | 3.74e-05 | 1.78e-01 | 0.1287 |
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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:00066444 | Liver | HCC | phospholipid metabolic process | 214/7958 | 383/18723 | 7.25e-08 | 1.48e-06 | 214 |
GO:001631121 | Liver | HCC | dephosphorylation | 230/7958 | 417/18723 | 1.00e-07 | 1.96e-06 | 230 |
GO:004648611 | Liver | HCC | glycerolipid metabolic process | 215/7958 | 392/18723 | 4.54e-07 | 7.49e-06 | 215 |
GO:003025821 | Liver | HCC | lipid modification | 123/7958 | 212/18723 | 3.50e-06 | 4.58e-05 | 123 |
GO:00066504 | Liver | HCC | glycerophospholipid metabolic process | 168/7958 | 306/18723 | 7.27e-06 | 8.62e-05 | 168 |
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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 |
MTMR11 | SNV | Missense_Mutation | c.1016N>T | p.Ser339Leu | p.S339L | A4FU01 | protein_coding | deleterious(0) | probably_damaging(0.986) | TCGA-A2-A0YK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |
MTMR11 | SNV | Missense_Mutation | c.95C>T | p.Pro32Leu | p.P32L | A4FU01 | protein_coding | tolerated(0.07) | benign(0) | TCGA-A8-A07O-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | CR | ||
MTMR11 | SNV | Missense_Mutation | rs373465441 | c.2056G>A | p.Asp686Asn | p.D686N | A4FU01 | protein_coding | tolerated_low_confidence(0.15) | benign(0.005) | TCGA-AR-A1AM-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | SD |
MTMR11 | SNV | Missense_Mutation | rs587625914 | c.772N>T | p.Arg258Cys | p.R258C | A4FU01 | protein_coding | deleterious(0) | benign(0.398) | TCGA-AR-A251-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | SD |
MTMR11 | SNV | Missense_Mutation | c.2089G>A | p.Ala697Thr | p.A697T | A4FU01 | protein_coding | tolerated_low_confidence(0.37) | benign(0) | TCGA-D8-A1XQ-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MTMR11 | insertion | Frame_Shift_Ins | rs587606143 | c.14_15insG | p.Arg6ProfsTer23 | p.R6Pfs*23 | A4FU01 | protein_coding | TCGA-A2-A0T2-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | xeloda | PD | ||
MTMR11 | insertion | Frame_Shift_Ins | novel | c.1751_1752insTATAGTTTTCTATGGGAATGAGGCGGATACAG | p.Leu585IlefsTer67 | p.L585Ifs*67 | A4FU01 | protein_coding | TCGA-AO-A0JB-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cyclophosphamide | SD | ||
MTMR11 | SNV | Missense_Mutation | novel | c.997G>A | p.Ala333Thr | p.A333T | A4FU01 | protein_coding | tolerated(0.4) | benign(0) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
MTMR11 | SNV | Missense_Mutation | novel | c.661G>A | p.Glu221Lys | p.E221K | A4FU01 | protein_coding | deleterious(0.01) | possibly_damaging(0.881) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
MTMR11 | SNV | Missense_Mutation | novel | c.314G>A | p.Arg105Gln | p.R105Q | A4FU01 | protein_coding | tolerated(0.19) | benign(0.003) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | 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 |
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