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Gene: UBOX5 |
Gene summary for UBOX5 |
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Gene information | Species | Human | Gene symbol | UBOX5 | Gene ID | 22888 |
Gene name | U-box domain containing 5 | |
Gene Alias | RNF37 | |
Cytomap | 20p13 | |
Gene Type | protein-coding | GO ID | GO:0000209 | UniProtAcc | O94941 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
22888 | UBOX5 | LZE4T | Human | Esophagus | ESCC | 1.59e-02 | 9.99e-02 | 0.0811 |
22888 | UBOX5 | P2T-E | Human | Esophagus | ESCC | 5.42e-04 | 8.95e-02 | 0.1177 |
22888 | UBOX5 | P4T-E | Human | Esophagus | ESCC | 3.68e-03 | 7.01e-02 | 0.1323 |
22888 | UBOX5 | P8T-E | Human | Esophagus | ESCC | 1.68e-05 | 7.05e-02 | 0.0889 |
22888 | UBOX5 | P9T-E | Human | Esophagus | ESCC | 3.46e-04 | 8.37e-02 | 0.1131 |
22888 | UBOX5 | P10T-E | Human | Esophagus | ESCC | 4.79e-06 | 1.19e-01 | 0.116 |
22888 | UBOX5 | P11T-E | Human | Esophagus | ESCC | 4.08e-04 | 1.52e-01 | 0.1426 |
22888 | UBOX5 | P12T-E | Human | Esophagus | ESCC | 3.97e-08 | 1.50e-01 | 0.1122 |
22888 | UBOX5 | P15T-E | Human | Esophagus | ESCC | 1.50e-05 | 1.30e-01 | 0.1149 |
22888 | UBOX5 | P16T-E | Human | Esophagus | ESCC | 5.74e-10 | 1.55e-01 | 0.1153 |
22888 | UBOX5 | P17T-E | Human | Esophagus | ESCC | 1.24e-02 | 1.64e-01 | 0.1278 |
22888 | UBOX5 | P20T-E | Human | Esophagus | ESCC | 9.71e-05 | 1.11e-01 | 0.1124 |
22888 | UBOX5 | P21T-E | Human | Esophagus | ESCC | 3.96e-05 | 1.26e-01 | 0.1617 |
22888 | UBOX5 | P22T-E | Human | Esophagus | ESCC | 5.05e-03 | 4.40e-02 | 0.1236 |
22888 | UBOX5 | P23T-E | Human | Esophagus | ESCC | 2.55e-09 | 1.75e-01 | 0.108 |
22888 | UBOX5 | P24T-E | Human | Esophagus | ESCC | 3.67e-04 | 9.56e-02 | 0.1287 |
22888 | UBOX5 | P26T-E | Human | Esophagus | ESCC | 3.68e-28 | 4.88e-01 | 0.1276 |
22888 | UBOX5 | P28T-E | Human | Esophagus | ESCC | 4.16e-02 | 9.78e-02 | 0.1149 |
22888 | UBOX5 | P30T-E | Human | Esophagus | ESCC | 2.59e-03 | 2.19e-01 | 0.137 |
22888 | UBOX5 | P31T-E | Human | Esophagus | ESCC | 6.77e-06 | 1.63e-01 | 0.1251 |
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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:000020917 | Esophagus | ESCC | protein polyubiquitination | 170/8552 | 236/18723 | 1.40e-16 | 1.09e-14 | 170 |
GO:000020921 | Liver | HCC | protein polyubiquitination | 151/7958 | 236/18723 | 1.90e-11 | 7.59e-10 | 151 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0412027 | Esophagus | ESCC | Ubiquitin mediated proteolysis | 122/4205 | 142/8465 | 6.53e-20 | 7.29e-18 | 3.74e-18 | 122 |
hsa0412036 | Esophagus | ESCC | Ubiquitin mediated proteolysis | 122/4205 | 142/8465 | 6.53e-20 | 7.29e-18 | 3.74e-18 | 122 |
hsa0412041 | Liver | HCC | Ubiquitin mediated proteolysis | 110/4020 | 142/8465 | 1.67e-13 | 3.74e-12 | 2.08e-12 | 110 |
hsa0412051 | Liver | HCC | Ubiquitin mediated proteolysis | 110/4020 | 142/8465 | 1.67e-13 | 3.74e-12 | 2.08e-12 | 110 |
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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 |
UBOX5 | SNV | Missense_Mutation | c.645N>T | p.Glu215Asp | p.E215D | O94941 | protein_coding | deleterious(0.05) | benign(0.009) | TCGA-D1-A17Q-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
UBOX5 | SNV | Missense_Mutation | rs368557466 | c.1529G>A | p.Arg510Gln | p.R510Q | O94941 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-E6-A1LX-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
UBOX5 | SNV | Missense_Mutation | rs374361254 | c.73G>A | p.Glu25Lys | p.E25K | O94941 | protein_coding | deleterious(0) | possibly_damaging(0.859) | TCGA-EO-A22R-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
UBOX5 | SNV | Missense_Mutation | novel | c.208N>A | p.Leu70Ile | p.L70I | O94941 | protein_coding | tolerated(0.22) | benign(0.012) | TCGA-EO-A3AZ-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
UBOX5 | SNV | Missense_Mutation | novel | c.413C>T | p.Ala138Val | p.A138V | O94941 | protein_coding | tolerated(0.09) | possibly_damaging(0.506) | TCGA-EO-A3B0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
UBOX5 | SNV | Missense_Mutation | novel | c.38G>T | p.Arg13Ile | p.R13I | O94941 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-EO-A3B0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
UBOX5 | SNV | Missense_Mutation | novel | c.38G>T | p.Arg13Ile | p.R13I | O94941 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-EY-A1GI-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
UBOX5 | SNV | Missense_Mutation | novel | c.1243N>A | p.Asp415Asn | p.D415N | O94941 | protein_coding | tolerated(0.07) | probably_damaging(0.947) | TCGA-FI-A2F4-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
UBOX5 | SNV | Missense_Mutation | novel | c.532N>G | p.Thr178Ala | p.T178A | O94941 | protein_coding | tolerated(0.26) | benign(0.047) | TCGA-4R-AA8I-01 | Liver | liver hepatocellular carcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
UBOX5 | SNV | Missense_Mutation | c.398N>G | p.His133Arg | p.H133R | O94941 | protein_coding | tolerated(0.11) | possibly_damaging(0.858) | TCGA-CC-A7IL-01 | Liver | liver hepatocellular carcinoma | Male | <65 | III/IV | Unknown | Unknown | 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 |
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