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Gene: METTL16 |
Gene summary for METTL16 |
Gene summary. |
Gene information | Species | Human | Gene symbol | METTL16 | Gene ID | 79066 |
Gene name | methyltransferase 16, N6-methyladenosine | |
Gene Alias | METT10D | |
Cytomap | 17p13.3 | |
Gene Type | protein-coding | GO ID | GO:0000154 | UniProtAcc | Q86W50 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
79066 | METTL16 | LZE4T | Human | Esophagus | ESCC | 3.91e-09 | 2.55e-01 | 0.0811 |
79066 | METTL16 | LZE5T | Human | Esophagus | ESCC | 6.11e-03 | 2.27e-01 | 0.0514 |
79066 | METTL16 | LZE7T | Human | Esophagus | ESCC | 2.37e-07 | 2.48e-01 | 0.0667 |
79066 | METTL16 | LZE8T | Human | Esophagus | ESCC | 1.46e-02 | 1.58e-01 | 0.067 |
79066 | METTL16 | LZE24T | Human | Esophagus | ESCC | 3.91e-10 | 3.44e-01 | 0.0596 |
79066 | METTL16 | P1T-E | Human | Esophagus | ESCC | 1.49e-10 | 3.45e-01 | 0.0875 |
79066 | METTL16 | P2T-E | Human | Esophagus | ESCC | 3.00e-21 | 3.36e-01 | 0.1177 |
79066 | METTL16 | P4T-E | Human | Esophagus | ESCC | 2.28e-13 | 3.68e-01 | 0.1323 |
79066 | METTL16 | P5T-E | Human | Esophagus | ESCC | 2.27e-06 | 1.47e-01 | 0.1327 |
79066 | METTL16 | P8T-E | Human | Esophagus | ESCC | 1.57e-10 | 2.38e-01 | 0.0889 |
79066 | METTL16 | P9T-E | Human | Esophagus | ESCC | 3.51e-08 | 1.94e-01 | 0.1131 |
79066 | METTL16 | P10T-E | Human | Esophagus | ESCC | 4.55e-15 | 2.66e-01 | 0.116 |
79066 | METTL16 | P11T-E | Human | Esophagus | ESCC | 1.05e-07 | 3.23e-01 | 0.1426 |
79066 | METTL16 | P12T-E | Human | Esophagus | ESCC | 2.38e-18 | 4.52e-01 | 0.1122 |
79066 | METTL16 | P15T-E | Human | Esophagus | ESCC | 5.68e-08 | 2.05e-01 | 0.1149 |
79066 | METTL16 | P16T-E | Human | Esophagus | ESCC | 4.02e-30 | 4.83e-01 | 0.1153 |
79066 | METTL16 | P20T-E | Human | Esophagus | ESCC | 2.98e-10 | 2.43e-01 | 0.1124 |
79066 | METTL16 | P21T-E | Human | Esophagus | ESCC | 5.34e-18 | 2.97e-01 | 0.1617 |
79066 | METTL16 | P22T-E | Human | Esophagus | ESCC | 1.14e-16 | 2.61e-01 | 0.1236 |
79066 | METTL16 | P23T-E | Human | Esophagus | ESCC | 5.06e-10 | 3.09e-01 | 0.108 |
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Transcriptomic changes along malignancy continuum. |
∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
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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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00800092 | Esophagus | ESCC | mRNA methylation | 14/8552 | 16/18723 | 6.78e-04 | 3.56e-03 | 14 |
GO:00165561 | Esophagus | ESCC | mRNA modification | 21/8552 | 27/18723 | 6.88e-04 | 3.61e-03 | 21 |
GO:0000154 | Esophagus | ESCC | rRNA modification | 26/8552 | 37/18723 | 2.16e-03 | 9.62e-03 | 26 |
GO:190236916 | Esophagus | ESCC | negative regulation of RNA catabolic process | 46/8552 | 75/18723 | 4.54e-03 | 1.78e-02 | 46 |
GO:003424914 | Esophagus | ESCC | negative regulation of cellular amide metabolic process | 144/8552 | 273/18723 | 1.08e-02 | 3.67e-02 | 144 |
GO:00098967 | Liver | NAFLD | positive regulation of catabolic process | 108/1882 | 492/18723 | 2.68e-15 | 3.14e-12 | 108 |
GO:00194396 | Liver | NAFLD | aromatic compound catabolic process | 102/1882 | 467/18723 | 2.29e-14 | 1.91e-11 | 102 |
GO:19013616 | Liver | NAFLD | organic cyclic compound catabolic process | 105/1882 | 495/18723 | 7.04e-14 | 5.15e-11 | 105 |
GO:00313317 | Liver | NAFLD | positive regulation of cellular catabolic process | 92/1882 | 427/18723 | 1.01e-12 | 4.91e-10 | 92 |
GO:00442707 | Liver | NAFLD | cellular nitrogen compound catabolic process | 93/1882 | 451/18723 | 1.04e-11 | 4.34e-09 | 93 |
GO:00467006 | Liver | NAFLD | heterocycle catabolic process | 92/1882 | 445/18723 | 1.16e-11 | 4.52e-09 | 92 |
GO:19033116 | Liver | NAFLD | regulation of mRNA metabolic process | 66/1882 | 288/18723 | 1.06e-10 | 2.96e-08 | 66 |
GO:00064026 | Liver | NAFLD | mRNA catabolic process | 56/1882 | 232/18723 | 3.49e-10 | 9.27e-08 | 56 |
GO:00346556 | Liver | NAFLD | nucleobase-containing compound catabolic process | 80/1882 | 407/18723 | 3.07e-09 | 4.61e-07 | 80 |
GO:00064016 | Liver | NAFLD | RNA catabolic process | 61/1882 | 278/18723 | 3.26e-09 | 4.76e-07 | 61 |
GO:00610136 | Liver | NAFLD | regulation of mRNA catabolic process | 42/1882 | 166/18723 | 1.27e-08 | 1.65e-06 | 42 |
GO:00098957 | Liver | NAFLD | negative regulation of catabolic process | 65/1882 | 320/18723 | 2.50e-08 | 2.71e-06 | 65 |
GO:00064177 | Liver | NAFLD | regulation of translation | 85/1882 | 468/18723 | 4.58e-08 | 4.54e-06 | 85 |
GO:00434886 | Liver | NAFLD | regulation of mRNA stability | 39/1882 | 158/18723 | 8.49e-08 | 7.09e-06 | 39 |
GO:00313307 | Liver | NAFLD | negative regulation of cellular catabolic process | 55/1882 | 262/18723 | 9.35e-08 | 7.59e-06 | 55 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
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 |
Annotation of somatic variants for genes involved in malignant transformation |
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 |
METTL16 | SNV | Missense_Mutation | c.706N>G | p.Leu236Val | p.L236V | Q86W50 | protein_coding | tolerated(0.1) | possibly_damaging(0.739) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
METTL16 | insertion | In_Frame_Ins | novel | c.212_213insGGCTCACTGCAACCTCCGCCTCCCAGGTTCGAGCGA | p.Pro71_Leu72insAlaHisCysAsnLeuArgLeuProGlySerSerGlu | p.P71_L72insAHCNLRLPGSSE | Q86W50 | protein_coding | TCGA-AN-A0FN-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
METTL16 | SNV | Missense_Mutation | novel | c.217G>C | p.Glu73Gln | p.E73Q | Q86W50 | protein_coding | deleterious(0.01) | probably_damaging(0.968) | TCGA-JW-A5VL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
METTL16 | SNV | Missense_Mutation | c.599N>A | p.Arg200Gln | p.R200Q | Q86W50 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
METTL16 | SNV | Missense_Mutation | c.851C>T | p.Ala284Val | p.A284V | Q86W50 | protein_coding | tolerated(0.06) | benign(0.057) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
METTL16 | SNV | Missense_Mutation | c.1262N>T | p.Glu421Val | p.E421V | Q86W50 | protein_coding | deleterious_low_confidence(0.02) | benign(0.078) | TCGA-DM-A28H-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | PD | |
METTL16 | SNV | Missense_Mutation | novel | c.929A>T | p.Lys310Ile | p.K310I | Q86W50 | protein_coding | deleterious(0) | possibly_damaging(0.818) | TCGA-G4-6295-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
METTL16 | SNV | Missense_Mutation | c.1115N>T | p.Thr372Met | p.T372M | Q86W50 | protein_coding | deleterious(0.02) | probably_damaging(0.975) | TCGA-AG-3742-01 | Colorectum | rectum adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
METTL16 | SNV | Missense_Mutation | rs765971942 | c.767N>T | p.Ala256Val | p.A256V | Q86W50 | protein_coding | deleterious(0.01) | benign(0.274) | TCGA-AG-3892-01 | Colorectum | rectum adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
METTL16 | SNV | Missense_Mutation | c.599N>A | p.Arg200Gln | p.R200Q | Q86W50 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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