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Gene: SUGP2 |
Gene summary for SUGP2 |
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Gene information | Species | Human | Gene symbol | SUGP2 | Gene ID | 10147 |
Gene name | SURP and G-patch domain containing 2 | |
Gene Alias | SFRS14 | |
Cytomap | 19p13.11 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q8IX01 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
10147 | SUGP2 | LZE4T | Human | Esophagus | ESCC | 4.77e-03 | 4.82e-02 | 0.0811 |
10147 | SUGP2 | LZE7T | Human | Esophagus | ESCC | 4.77e-15 | 7.98e-01 | 0.0667 |
10147 | SUGP2 | LZE21D1 | Human | Esophagus | HGIN | 8.09e-03 | 3.62e-01 | 0.0632 |
10147 | SUGP2 | LZE24T | Human | Esophagus | ESCC | 5.61e-09 | 2.49e-01 | 0.0596 |
10147 | SUGP2 | LZE21T | Human | Esophagus | ESCC | 1.16e-02 | 3.15e-01 | 0.0655 |
10147 | SUGP2 | LZE6T | Human | Esophagus | ESCC | 4.25e-02 | 1.26e-01 | 0.0845 |
10147 | SUGP2 | P1T-E | Human | Esophagus | ESCC | 6.29e-06 | 4.01e-01 | 0.0875 |
10147 | SUGP2 | P2T-E | Human | Esophagus | ESCC | 1.32e-11 | 1.71e-01 | 0.1177 |
10147 | SUGP2 | P4T-E | Human | Esophagus | ESCC | 1.84e-11 | 2.04e-01 | 0.1323 |
10147 | SUGP2 | P5T-E | Human | Esophagus | ESCC | 1.10e-12 | 8.47e-02 | 0.1327 |
10147 | SUGP2 | P8T-E | Human | Esophagus | ESCC | 1.19e-17 | 2.25e-01 | 0.0889 |
10147 | SUGP2 | P9T-E | Human | Esophagus | ESCC | 6.11e-11 | 2.39e-01 | 0.1131 |
10147 | SUGP2 | P10T-E | Human | Esophagus | ESCC | 5.05e-26 | 4.68e-01 | 0.116 |
10147 | SUGP2 | P11T-E | Human | Esophagus | ESCC | 6.07e-09 | 2.82e-01 | 0.1426 |
10147 | SUGP2 | P12T-E | Human | Esophagus | ESCC | 9.32e-18 | 2.42e-01 | 0.1122 |
10147 | SUGP2 | P15T-E | Human | Esophagus | ESCC | 9.74e-12 | 1.75e-01 | 0.1149 |
10147 | SUGP2 | P16T-E | Human | Esophagus | ESCC | 1.51e-11 | 7.04e-02 | 0.1153 |
10147 | SUGP2 | P17T-E | Human | Esophagus | ESCC | 3.02e-02 | 1.29e-01 | 0.1278 |
10147 | SUGP2 | P19T-E | Human | Esophagus | ESCC | 1.21e-02 | 2.21e-01 | 0.1662 |
10147 | SUGP2 | P20T-E | Human | Esophagus | ESCC | 2.94e-11 | 1.39e-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 |
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:000838026 | Esophagus | HGIN | RNA splicing | 160/2587 | 434/18723 | 3.74e-34 | 1.12e-30 | 160 |
GO:0008380111 | Esophagus | ESCC | RNA splicing | 336/8552 | 434/18723 | 1.74e-42 | 3.67e-39 | 336 |
GO:00083807 | Liver | NAFLD | RNA splicing | 70/1882 | 434/18723 | 4.62e-05 | 1.10e-03 | 70 |
GO:000838022 | Liver | HCC | RNA splicing | 313/7958 | 434/18723 | 1.36e-36 | 1.73e-33 | 313 |
GO:000838020 | Oral cavity | OSCC | RNA splicing | 308/7305 | 434/18723 | 2.43e-42 | 7.70e-39 | 308 |
GO:000838025 | Oral cavity | EOLP | RNA splicing | 115/2218 | 434/18723 | 2.24e-17 | 3.04e-14 | 115 |
GO:0008380113 | Thyroid | PTC | RNA splicing | 273/5968 | 434/18723 | 4.44e-41 | 1.40e-37 | 273 |
GO:000838034 | Thyroid | ATC | RNA splicing | 270/6293 | 434/18723 | 7.50e-35 | 1.19e-31 | 270 |
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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 |
SUGP2 | SNV | Missense_Mutation | novel | c.2797A>C | p.Thr933Pro | p.T933P | protein_coding | tolerated(0.58) | benign(0) | TCGA-A2-A0D1-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | taxotere | SD | |
SUGP2 | SNV | Missense_Mutation | c.2698N>C | p.Glu900Gln | p.E900Q | protein_coding | tolerated(0.11) | benign(0.031) | TCGA-A8-A0A7-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
SUGP2 | SNV | Missense_Mutation | novel | c.2797N>C | p.Thr933Pro | p.T933P | protein_coding | tolerated(0.58) | benign(0) | TCGA-AR-A1AX-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |
SUGP2 | SNV | Missense_Mutation | c.1058N>C | p.His353Pro | p.H353P | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-BH-A0BZ-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | CR | ||
SUGP2 | SNV | Missense_Mutation | novel | c.2857N>A | p.Leu953Met | p.L953M | protein_coding | tolerated(0.15) | possibly_damaging(0.495) | TCGA-BH-A0E2-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | SD | |
SUGP2 | SNV | Missense_Mutation | c.260G>C | p.Arg87Thr | p.R87T | protein_coding | deleterious_low_confidence(0.01) | benign(0.258) | TCGA-E2-A10C-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | ||
SUGP2 | SNV | Missense_Mutation | c.3023N>T | p.Ser1008Phe | p.S1008F | protein_coding | deleterious(0) | possibly_damaging(0.601) | TCGA-E9-A1RF-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | tamoxiphen | SD | ||
SUGP2 | SNV | Missense_Mutation | rs375174157 | c.1984G>A | p.Asp662Asn | p.D662N | protein_coding | tolerated(0.13) | benign(0.378) | TCGA-UL-AAZ6-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | herceptin | SD | |
SUGP2 | insertion | Nonsense_Mutation | novel | c.3189_3190insTTTTCCTTGTAAAAGATGAAAAACCAAACCCAGATGT | p.Glu1064PhefsTer4 | p.E1064Ffs*4 | protein_coding | TCGA-AN-A03Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |||
SUGP2 | insertion | In_Frame_Ins | novel | c.2855_2856insACACACACAAGATACACA | p.Ala952_Leu953insHisThrGlnAspThrHis | p.A952_L953insHTQDTH | protein_coding | TCGA-BH-A0E2-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | 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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