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Gene: TMLHE |
Gene summary for TMLHE |
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Gene information | Species | Human | Gene symbol | TMLHE | Gene ID | 55217 |
Gene name | trimethyllysine hydroxylase, epsilon | |
Gene Alias | AUTSX6 | |
Cytomap | Xq28 | |
Gene Type | protein-coding | GO ID | GO:0006575 | UniProtAcc | Q9NVH6 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55217 | TMLHE | LZE4T | Human | Esophagus | ESCC | 3.75e-06 | 1.78e-01 | 0.0811 |
55217 | TMLHE | LZE7T | Human | Esophagus | ESCC | 6.92e-05 | 3.20e-01 | 0.0667 |
55217 | TMLHE | LZE24T | Human | Esophagus | ESCC | 9.08e-11 | 3.34e-01 | 0.0596 |
55217 | TMLHE | LZE21T | Human | Esophagus | ESCC | 1.25e-02 | 2.39e-01 | 0.0655 |
55217 | TMLHE | P1T-E | Human | Esophagus | ESCC | 2.11e-03 | 3.34e-01 | 0.0875 |
55217 | TMLHE | P2T-E | Human | Esophagus | ESCC | 1.39e-35 | 6.39e-01 | 0.1177 |
55217 | TMLHE | P4T-E | Human | Esophagus | ESCC | 6.56e-13 | 3.61e-01 | 0.1323 |
55217 | TMLHE | P5T-E | Human | Esophagus | ESCC | 3.23e-02 | 1.06e-01 | 0.1327 |
55217 | TMLHE | P8T-E | Human | Esophagus | ESCC | 1.59e-12 | 2.39e-01 | 0.0889 |
55217 | TMLHE | P9T-E | Human | Esophagus | ESCC | 4.10e-09 | 1.94e-01 | 0.1131 |
55217 | TMLHE | P10T-E | Human | Esophagus | ESCC | 2.13e-19 | 3.38e-01 | 0.116 |
55217 | TMLHE | P11T-E | Human | Esophagus | ESCC | 4.15e-03 | 2.66e-01 | 0.1426 |
55217 | TMLHE | P12T-E | Human | Esophagus | ESCC | 8.43e-18 | 3.55e-01 | 0.1122 |
55217 | TMLHE | P15T-E | Human | Esophagus | ESCC | 2.50e-08 | 1.89e-01 | 0.1149 |
55217 | TMLHE | P16T-E | Human | Esophagus | ESCC | 1.28e-09 | 1.99e-01 | 0.1153 |
55217 | TMLHE | P20T-E | Human | Esophagus | ESCC | 2.57e-14 | 3.33e-01 | 0.1124 |
55217 | TMLHE | P21T-E | Human | Esophagus | ESCC | 1.11e-16 | 3.20e-01 | 0.1617 |
55217 | TMLHE | P22T-E | Human | Esophagus | ESCC | 1.03e-32 | 5.78e-01 | 0.1236 |
55217 | TMLHE | P23T-E | Human | Esophagus | ESCC | 1.19e-20 | 4.59e-01 | 0.108 |
55217 | TMLHE | P24T-E | Human | Esophagus | ESCC | 7.72e-09 | 1.87e-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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:00065757 | Esophagus | ESCC | cellular modified amino acid metabolic process | 112/8552 | 188/18723 | 8.31e-05 | 6.06e-04 | 112 |
GO:00423986 | Esophagus | ESCC | cellular modified amino acid biosynthetic process | 34/8552 | 46/18723 | 9.39e-05 | 6.70e-04 | 34 |
GO:000657521 | Liver | HCC | cellular modified amino acid metabolic process | 119/7958 | 188/18723 | 6.47e-09 | 1.67e-07 | 119 |
GO:004239821 | Liver | HCC | cellular modified amino acid biosynthetic process | 34/7958 | 46/18723 | 1.53e-05 | 1.67e-04 | 34 |
GO:0006577 | Liver | HCC | amino-acid betaine metabolic process | 13/7958 | 17/18723 | 4.77e-03 | 2.02e-02 | 13 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0031010 | Esophagus | ESCC | Lysine degradation | 41/4205 | 63/8465 | 9.63e-03 | 2.27e-02 | 1.16e-02 | 41 |
hsa0031013 | Esophagus | ESCC | Lysine degradation | 41/4205 | 63/8465 | 9.63e-03 | 2.27e-02 | 1.16e-02 | 41 |
hsa0031041 | Liver | HCC | Lysine degradation | 47/4020 | 63/8465 | 1.02e-05 | 7.58e-05 | 4.22e-05 | 47 |
hsa0031051 | Liver | HCC | Lysine degradation | 47/4020 | 63/8465 | 1.02e-05 | 7.58e-05 | 4.22e-05 | 47 |
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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 |
TMLHE | SNV | Missense_Mutation | rs145371120 | c.278N>A | p.Arg93His | p.R93H | Q9NVH6 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-BR-A4QL-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | xeloda | CR |
TMLHE | SNV | Missense_Mutation | c.905N>C | p.Ile302Thr | p.I302T | Q9NVH6 | protein_coding | deleterious(0.02) | possibly_damaging(0.516) | TCGA-CG-4474-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
TMLHE | SNV | Missense_Mutation | novel | c.701A>G | p.Tyr234Cys | p.Y234C | Q9NVH6 | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-VQ-A924-01 | Stomach | stomach adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
TMLHE | SNV | Missense_Mutation | novel | c.25C>A | p.Leu9Ile | p.L9I | Q9NVH6 | protein_coding | tolerated_low_confidence(0.07) | benign(0.001) | TCGA-VQ-A925-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | PD |
TMLHE | SNV | Missense_Mutation | novel | c.121N>G | p.Trp41Gly | p.W41G | Q9NVH6 | protein_coding | tolerated_low_confidence(0.27) | benign(0) | TCGA-KS-A4I1-01 | Thyroid | thyroid carcinoma | Female | <65 | I/II | Hormone Therapy | cytomel | CR |
TMLHE | insertion | Frame_Shift_Ins | novel | c.6_7insCAAATATTTCT | p.Tyr3GlnfsTer19 | p.Y3Qfs*19 | Q9NVH6 | protein_coding | TCGA-FY-A4B0-01 | Thyroid | thyroid carcinoma | Male | >=65 | I/II | Hormone Therapy | synthroid | 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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