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Gene: MT1H |
Gene summary for MT1H |
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Gene information | Species | Human | Gene symbol | MT1H | Gene ID | 4496 |
Gene name | metallothionein 1H | |
Gene Alias | MT-0 | |
Cytomap | 16q13 | |
Gene Type | protein-coding | GO ID | GO:0006873 | UniProtAcc | A0A140VJP7 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
4496 | MT1H | HTA11_2487_2000001011 | Human | Colorectum | SER | 6.06e-04 | 3.18e-01 | -0.1808 |
4496 | MT1H | HTA11_347_2000001011 | Human | Colorectum | AD | 1.25e-02 | 1.87e-01 | -0.1954 |
4496 | MT1H | HTA11_411_2000001011 | Human | Colorectum | SER | 2.71e-02 | 5.15e-01 | -0.2602 |
4496 | MT1H | HTA11_3361_2000001011 | Human | Colorectum | AD | 4.78e-04 | 3.96e-01 | -0.1207 |
4496 | MT1H | HTA11_866_2000001011 | Human | Colorectum | AD | 3.42e-06 | 3.15e-01 | -0.1001 |
4496 | MT1H | HTA11_2992_2000001011 | Human | Colorectum | SER | 5.47e-03 | 5.04e-01 | -0.1706 |
4496 | MT1H | HTA11_5212_2000001011 | Human | Colorectum | AD | 8.84e-17 | 1.36e+00 | -0.2061 |
4496 | MT1H | HTA11_546_2000001011 | Human | Colorectum | AD | 1.60e-03 | 3.79e-01 | -0.0842 |
4496 | MT1H | P4T-E | Human | Esophagus | ESCC | 2.90e-03 | 4.61e-01 | 0.1323 |
4496 | MT1H | P5T-E | Human | Esophagus | ESCC | 7.90e-03 | 1.07e-01 | 0.1327 |
4496 | MT1H | P20T-E | Human | Esophagus | ESCC | 2.18e-13 | 3.32e-01 | 0.1124 |
4496 | MT1H | P24T-E | Human | Esophagus | ESCC | 1.78e-03 | 2.48e-01 | 0.1287 |
4496 | MT1H | P27T-E | Human | Esophagus | ESCC | 1.88e-04 | 1.74e-01 | 0.1055 |
4496 | MT1H | P31T-E | Human | Esophagus | ESCC | 3.60e-13 | 8.11e-01 | 0.1251 |
4496 | MT1H | P80T-E | Human | Esophagus | ESCC | 1.30e-10 | 7.46e-01 | 0.155 |
4496 | MT1H | P104T-E | Human | Esophagus | ESCC | 3.26e-14 | 1.26e+00 | 0.0931 |
4496 | MT1H | P107T-E | Human | Esophagus | ESCC | 4.67e-06 | 1.72e-01 | 0.171 |
4496 | MT1H | P128T-E | Human | Esophagus | ESCC | 9.84e-83 | 5.75e+00 | 0.1241 |
4496 | MT1H | P130T-E | Human | Esophagus | ESCC | 3.02e-26 | 2.25e+00 | 0.1676 |
4496 | MT1H | Pat01-B | Human | Stomach | GC | 5.44e-03 | 2.34e-01 | 0.5754 |
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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:0009636 | Colorectum | AD | response to toxic substance | 88/3918 | 262/18723 | 1.12e-06 | 3.72e-05 | 88 |
GO:0055076 | Colorectum | AD | transition metal ion homeostasis | 53/3918 | 138/18723 | 1.89e-06 | 5.65e-05 | 53 |
GO:0046916 | Colorectum | AD | cellular transition metal ion homeostasis | 43/3918 | 115/18723 | 3.62e-05 | 6.56e-04 | 43 |
GO:0098754 | Colorectum | AD | detoxification | 53/3918 | 152/18723 | 4.63e-05 | 7.98e-04 | 53 |
GO:0046686 | Colorectum | AD | response to cadmium ion | 27/3918 | 68/18723 | 3.19e-04 | 3.80e-03 | 27 |
GO:0010038 | Colorectum | AD | response to metal ion | 106/3918 | 373/18723 | 3.22e-04 | 3.83e-03 | 106 |
GO:0055069 | Colorectum | AD | zinc ion homeostasis | 18/3918 | 40/18723 | 5.36e-04 | 5.74e-03 | 18 |
GO:0071276 | Colorectum | AD | cellular response to cadmium ion | 18/3918 | 40/18723 | 5.36e-04 | 5.74e-03 | 18 |
GO:0071248 | Colorectum | AD | cellular response to metal ion | 61/3918 | 197/18723 | 5.74e-04 | 6.09e-03 | 61 |
GO:0071241 | Colorectum | AD | cellular response to inorganic substance | 68/3918 | 226/18723 | 6.98e-04 | 7.10e-03 | 68 |
GO:0006882 | Colorectum | AD | cellular zinc ion homeostasis | 17/3918 | 38/18723 | 8.26e-04 | 8.13e-03 | 17 |
GO:0097501 | Colorectum | AD | stress response to metal ion | 10/3918 | 19/18723 | 2.25e-03 | 1.77e-02 | 10 |
GO:0045926 | Colorectum | AD | negative regulation of growth | 70/3918 | 249/18723 | 4.07e-03 | 2.83e-02 | 70 |
GO:0071294 | Colorectum | AD | cellular response to zinc ion | 11/3918 | 24/18723 | 5.43e-03 | 3.55e-02 | 11 |
GO:0010273 | Colorectum | AD | detoxification of copper ion | 8/3918 | 15/18723 | 5.67e-03 | 3.64e-02 | 8 |
GO:1990169 | Colorectum | AD | stress response to copper ion | 8/3918 | 15/18723 | 5.67e-03 | 3.64e-02 | 8 |
GO:0071280 | Colorectum | AD | cellular response to copper ion | 12/3918 | 28/18723 | 7.21e-03 | 4.39e-02 | 12 |
GO:0046688 | Colorectum | AD | response to copper ion | 16/3918 | 42/18723 | 8.10e-03 | 4.76e-02 | 16 |
GO:00096361 | Colorectum | SER | response to toxic substance | 71/2897 | 262/18723 | 8.63e-07 | 4.07e-05 | 71 |
GO:00987541 | Colorectum | SER | detoxification | 46/2897 | 152/18723 | 3.02e-06 | 1.20e-04 | 46 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa04978 | Stomach | GC | Mineral absorption | 15/708 | 60/8465 | 8.88e-05 | 9.80e-04 | 6.90e-04 | 15 |
hsa049781 | Stomach | GC | Mineral absorption | 15/708 | 60/8465 | 8.88e-05 | 9.80e-04 | 6.90e-04 | 15 |
hsa049784 | Stomach | CSG | Mineral absorption | 11/633 | 60/8465 | 4.40e-03 | 2.53e-02 | 1.82e-02 | 11 |
hsa049785 | Stomach | CSG | Mineral absorption | 11/633 | 60/8465 | 4.40e-03 | 2.53e-02 | 1.82e-02 | 11 |
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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 |
MT1H | SNV | Missense_Mutation | c.112N>A | p.Pro38Thr | p.P38T | P80294 | protein_coding | deleterious(0.03) | benign(0.27) | TCGA-FU-A3HZ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
MT1H | SNV | Missense_Mutation | c.22N>A | p.Glu8Lys | p.E8K | P80294 | protein_coding | tolerated(0.15) | benign(0.019) | TCGA-VS-A958-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
MT1H | SNV | Missense_Mutation | c.95N>A | p.Ser32Asn | p.S32N | P80294 | protein_coding | tolerated(0.06) | benign(0.218) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD | |
MT1H | SNV | Missense_Mutation | c.158C>T | p.Ala53Val | p.A53V | P80294 | protein_coding | deleterious(0.04) | benign(0) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
MT1H | SNV | Missense_Mutation | c.158C>G | p.Ala53Gly | p.A53G | P80294 | protein_coding | tolerated(0.14) | benign(0.072) | TCGA-75-6214-01 | Lung | lung adenocarcinoma | Female | Unknown | III/IV | Unknown | Unknown | PD | |
MT1H | SNV | Missense_Mutation | c.94A>T | p.Ser32Cys | p.S32C | P80294 | protein_coding | deleterious(0) | possibly_damaging(0.865) | TCGA-NJ-A4YI-01 | Lung | lung adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
MT1H | SNV | Missense_Mutation | novel | c.88N>G | p.Lys30Glu | p.K30E | P80294 | protein_coding | deleterious(0.02) | probably_damaging(0.945) | TCGA-21-1082-01 | Lung | lung squamous cell carcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
MT1H | SNV | Missense_Mutation | c.83C>A | p.Ser28Tyr | p.S28Y | P80294 | protein_coding | deleterious(0) | probably_damaging(0.995) | TCGA-56-8628-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
MT1H | SNV | Missense_Mutation | novel | c.101G>A | p.Cys34Tyr | p.C34Y | P80294 | protein_coding | deleterious(0.04) | probably_damaging(0.995) | TCGA-77-7465-01 | Lung | lung squamous cell carcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
MT1H | SNV | Missense_Mutation | novel | c.37N>C | p.Cys13Arg | p.C13R | P80294 | protein_coding | deleterious(0) | possibly_damaging(0.848) | TCGA-CN-A498-01 | Oral cavity | head & neck squamous cell carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | PD |
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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 |
4496 | MT1H | NA | GLUCOCORTICOID | 11713267 | ||
4496 | MT1H | NA | CISPLATIN | CISPLATIN | 10422815 | |
4496 | MT1H | NA | H2O2 | 8385930 | ||
4496 | MT1H | NA | STREPTOZOTOCIN | STREPTOZOCIN | 9176863 | |
4496 | MT1H | NA | SELENIUM | 3309208 | ||
4496 | MT1H | NA | HORMONES | 15196976 | ||
4496 | MT1H | NA | 6-AN | 11835189 |
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