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Gene: THYN1 |
Gene summary for THYN1 |
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Gene information | Species | Human | Gene symbol | THYN1 | Gene ID | 29087 |
Gene name | thymocyte nuclear protein 1 | |
Gene Alias | HSPC144 | |
Cytomap | 11q25 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | Q9P016 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
29087 | THYN1 | LZE4T | Human | Esophagus | ESCC | 1.97e-03 | 2.33e-01 | 0.0811 |
29087 | THYN1 | LZE7T | Human | Esophagus | ESCC | 4.39e-09 | 7.43e-01 | 0.0667 |
29087 | THYN1 | LZE8T | Human | Esophagus | ESCC | 6.95e-03 | 1.19e-01 | 0.067 |
29087 | THYN1 | LZE20T | Human | Esophagus | ESCC | 4.98e-02 | 1.68e-01 | 0.0662 |
29087 | THYN1 | LZE24T | Human | Esophagus | ESCC | 5.45e-32 | 9.09e-01 | 0.0596 |
29087 | THYN1 | LZE6T | Human | Esophagus | ESCC | 2.35e-04 | 2.37e-01 | 0.0845 |
29087 | THYN1 | P1T-E | Human | Esophagus | ESCC | 4.05e-04 | 3.92e-01 | 0.0875 |
29087 | THYN1 | P2T-E | Human | Esophagus | ESCC | 2.71e-18 | 2.45e-01 | 0.1177 |
29087 | THYN1 | P4T-E | Human | Esophagus | ESCC | 3.50e-66 | 1.84e+00 | 0.1323 |
29087 | THYN1 | P5T-E | Human | Esophagus | ESCC | 1.93e-23 | 4.42e-01 | 0.1327 |
29087 | THYN1 | P8T-E | Human | Esophagus | ESCC | 5.30e-31 | 5.05e-01 | 0.0889 |
29087 | THYN1 | P9T-E | Human | Esophagus | ESCC | 1.68e-19 | 5.48e-01 | 0.1131 |
29087 | THYN1 | P10T-E | Human | Esophagus | ESCC | 2.08e-54 | 9.67e-01 | 0.116 |
29087 | THYN1 | P11T-E | Human | Esophagus | ESCC | 7.75e-14 | 6.54e-01 | 0.1426 |
29087 | THYN1 | P12T-E | Human | Esophagus | ESCC | 7.34e-45 | 7.14e-01 | 0.1122 |
29087 | THYN1 | P15T-E | Human | Esophagus | ESCC | 2.50e-14 | 3.59e-01 | 0.1149 |
29087 | THYN1 | P16T-E | Human | Esophagus | ESCC | 3.78e-30 | 5.99e-01 | 0.1153 |
29087 | THYN1 | P17T-E | Human | Esophagus | ESCC | 4.72e-08 | 3.26e-01 | 0.1278 |
29087 | THYN1 | P19T-E | Human | Esophagus | ESCC | 2.56e-02 | 4.69e-01 | 0.1662 |
29087 | THYN1 | P20T-E | Human | Esophagus | ESCC | 8.45e-27 | 5.19e-01 | 0.1124 |
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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 |
Oral cavity | OSCC | ![]() |
Oral cavity | LP | ![]() |
Oral cavity | EOLP | ![]() |
Oral cavity | NEOLP | ![]() |
Esophagus | HGIN | ![]() |
∗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 |
THYN1 | SNV | Missense_Mutation | c.74C>A | p.Thr25Asn | p.T25N | Q9P016 | protein_coding | tolerated(0.07) | benign(0.127) | TCGA-A2-A25A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Cytoxan | SD | |
THYN1 | SNV | Missense_Mutation | rs202070344 | c.544C>T | p.His182Tyr | p.H182Y | Q9P016 | protein_coding | tolerated(0.29) | benign(0.029) | TCGA-EK-A2RJ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
THYN1 | SNV | Missense_Mutation | rs778350333 | c.370N>A | p.Ala124Thr | p.A124T | Q9P016 | protein_coding | tolerated(0.08) | probably_damaging(0.948) | TCGA-5M-AAT6-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Unknown | Unknown | PD |
THYN1 | SNV | Missense_Mutation | c.103N>C | p.Val35Leu | p.V35L | Q9P016 | protein_coding | tolerated(0.36) | benign(0) | TCGA-A6-6653-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
THYN1 | SNV | Missense_Mutation | c.140A>T | p.Lys47Ile | p.K47I | Q9P016 | protein_coding | tolerated(0.06) | benign(0.005) | TCGA-CA-6718-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
THYN1 | SNV | Missense_Mutation | c.292G>A | p.Ala98Thr | p.A98T | Q9P016 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
THYN1 | SNV | Missense_Mutation | rs753894768 | c.507G>T | p.Met169Ile | p.M169I | Q9P016 | protein_coding | tolerated(0.12) | benign(0.04) | TCGA-EI-6917-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5fluorouracil+oxaciplatina+l-folinian | SD |
THYN1 | deletion | Frame_Shift_Del | c.581delN | p.Asn194IlefsTer15 | p.N194Ifs*15 | Q9P016 | protein_coding | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |||
THYN1 | deletion | Frame_Shift_Del | c.581delN | p.Asn194IlefsTer15 | p.N194Ifs*15 | Q9P016 | protein_coding | TCGA-AD-5900-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |||
THYN1 | SNV | Missense_Mutation | novel | c.243N>C | p.Lys81Asn | p.K81N | Q9P016 | protein_coding | deleterious(0.02) | possibly_damaging(0.461) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | 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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