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Gene: XPO5 |
Gene summary for XPO5 |
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Gene information | Species | Human | Gene symbol | XPO5 | Gene ID | 57510 |
Gene name | exportin 5 | |
Gene Alias | exp5 | |
Cytomap | 6p21.1 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q9HAV4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
57510 | XPO5 | GSM6177620_NYU_UCEC1_lib1_lib1 | Human | Endometrium | EEC | 2.02e-05 | 1.19e-01 | -0.1869 |
57510 | XPO5 | GSM6177620_NYU_UCEC1_lib2_lib2 | Human | Endometrium | EEC | 9.29e-03 | 8.55e-02 | -0.1875 |
57510 | XPO5 | GSM6177620_NYU_UCEC1_lib3_lib3 | Human | Endometrium | EEC | 1.44e-07 | 8.19e-02 | -0.1883 |
57510 | XPO5 | GSM6177621_NYU_UCEC2_lib1_lib1 | Human | Endometrium | EEC | 1.65e-03 | 1.01e-01 | -0.1934 |
57510 | XPO5 | GSM6177622_NYU_UCEC3_lib1_lib1 | Human | Endometrium | EEC | 2.71e-06 | 1.62e-02 | -0.1917 |
57510 | XPO5 | GSM6177622_NYU_UCEC3_lib2_lib2 | Human | Endometrium | EEC | 9.48e-04 | 1.57e-02 | -0.1916 |
57510 | XPO5 | GSM6177623_NYU_UCEC3_Vis | Human | Endometrium | EEC | 2.14e-03 | 1.73e-01 | -0.1269 |
57510 | XPO5 | LZE2T | Human | Esophagus | ESCC | 5.33e-10 | 1.34e+00 | 0.082 |
57510 | XPO5 | LZE4T | Human | Esophagus | ESCC | 3.81e-02 | 1.24e-01 | 0.0811 |
57510 | XPO5 | LZE7T | Human | Esophagus | ESCC | 2.62e-03 | 2.70e-01 | 0.0667 |
57510 | XPO5 | LZE24T | Human | Esophagus | ESCC | 4.62e-11 | 1.84e-01 | 0.0596 |
57510 | XPO5 | P2T-E | Human | Esophagus | ESCC | 2.89e-14 | 2.29e-01 | 0.1177 |
57510 | XPO5 | P4T-E | Human | Esophagus | ESCC | 5.83e-08 | 2.50e-01 | 0.1323 |
57510 | XPO5 | P5T-E | Human | Esophagus | ESCC | 9.74e-11 | 2.28e-01 | 0.1327 |
57510 | XPO5 | P8T-E | Human | Esophagus | ESCC | 2.31e-05 | 7.60e-02 | 0.0889 |
57510 | XPO5 | P9T-E | Human | Esophagus | ESCC | 1.71e-05 | 1.80e-01 | 0.1131 |
57510 | XPO5 | P10T-E | Human | Esophagus | ESCC | 6.10e-06 | 1.98e-01 | 0.116 |
57510 | XPO5 | P11T-E | Human | Esophagus | ESCC | 8.44e-04 | 1.74e-01 | 0.1426 |
57510 | XPO5 | P12T-E | Human | Esophagus | ESCC | 3.10e-09 | 2.09e-01 | 0.1122 |
57510 | XPO5 | P15T-E | Human | Esophagus | ESCC | 1.56e-05 | 1.88e-01 | 0.1149 |
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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:000640315 | Endometrium | EEC | RNA localization | 53/2168 | 201/18723 | 5.20e-09 | 3.47e-07 | 53 |
GO:000661114 | Endometrium | EEC | protein export from nucleus | 20/2168 | 57/18723 | 2.96e-06 | 8.25e-05 | 20 |
GO:005065712 | Endometrium | EEC | nucleic acid transport | 39/2168 | 163/18723 | 7.00e-06 | 1.63e-04 | 39 |
GO:005065812 | Endometrium | EEC | RNA transport | 39/2168 | 163/18723 | 7.00e-06 | 1.63e-04 | 39 |
GO:005123612 | Endometrium | EEC | establishment of RNA localization | 39/2168 | 166/18723 | 1.11e-05 | 2.33e-04 | 39 |
GO:000691314 | Endometrium | EEC | nucleocytoplasmic transport | 59/2168 | 301/18723 | 3.31e-05 | 5.65e-04 | 59 |
GO:005116914 | Endometrium | EEC | nuclear transport | 59/2168 | 301/18723 | 3.31e-05 | 5.65e-04 | 59 |
GO:001593112 | Endometrium | EEC | nucleobase-containing compound transport | 46/2168 | 222/18723 | 5.91e-05 | 9.13e-04 | 46 |
GO:005116814 | Endometrium | EEC | nuclear export | 35/2168 | 154/18723 | 6.36e-05 | 9.48e-04 | 35 |
GO:001058613 | Endometrium | EEC | miRNA metabolic process | 11/2168 | 27/18723 | 1.08e-04 | 1.49e-03 | 11 |
GO:003466012 | Esophagus | ESCC | ncRNA metabolic process | 346/8552 | 485/18723 | 4.35e-31 | 2.51e-28 | 346 |
GO:0006913110 | Esophagus | ESCC | nucleocytoplasmic transport | 230/8552 | 301/18723 | 6.04e-28 | 2.02e-25 | 230 |
GO:0051169110 | Esophagus | ESCC | nuclear transport | 230/8552 | 301/18723 | 6.04e-28 | 2.02e-25 | 230 |
GO:0006403110 | Esophagus | ESCC | RNA localization | 166/8552 | 201/18723 | 1.95e-27 | 6.18e-25 | 166 |
GO:005123617 | Esophagus | ESCC | establishment of RNA localization | 134/8552 | 166/18723 | 1.23e-20 | 1.81e-18 | 134 |
GO:0051168110 | Esophagus | ESCC | nuclear export | 126/8552 | 154/18723 | 1.88e-20 | 2.65e-18 | 126 |
GO:005065717 | Esophagus | ESCC | nucleic acid transport | 131/8552 | 163/18723 | 6.94e-20 | 8.46e-18 | 131 |
GO:005065817 | Esophagus | ESCC | RNA transport | 131/8552 | 163/18723 | 6.94e-20 | 8.46e-18 | 131 |
GO:001593117 | Esophagus | ESCC | nucleobase-containing compound transport | 162/8552 | 222/18723 | 9.87e-17 | 7.93e-15 | 162 |
GO:000640512 | Esophagus | ESCC | RNA export from nucleus | 68/8552 | 84/18723 | 2.99e-11 | 1.01e-09 | 68 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0301321 | Esophagus | ESCC | Nucleocytoplasmic transport | 89/4205 | 108/8465 | 1.20e-12 | 2.37e-11 | 1.21e-11 | 89 |
hsa0301331 | Esophagus | ESCC | Nucleocytoplasmic transport | 89/4205 | 108/8465 | 1.20e-12 | 2.37e-11 | 1.21e-11 | 89 |
hsa03013 | Liver | HCC | Nucleocytoplasmic transport | 81/4020 | 108/8465 | 4.28e-09 | 6.83e-08 | 3.80e-08 | 81 |
hsa030131 | Liver | HCC | Nucleocytoplasmic transport | 81/4020 | 108/8465 | 4.28e-09 | 6.83e-08 | 3.80e-08 | 81 |
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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 |
XPO5 | SNV | Missense_Mutation | rs762469874 | c.1783N>T | p.Arg595Trp | p.R595W | Q9HAV4 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-A2-A0YJ-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cytoxan | PD |
XPO5 | SNV | Missense_Mutation | novel | c.2304N>C | p.Gln768His | p.Q768H | Q9HAV4 | protein_coding | tolerated(0.68) | benign(0) | TCGA-A2-A0YM-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
XPO5 | SNV | Missense_Mutation | c.1913N>C | p.Leu638Pro | p.L638P | Q9HAV4 | protein_coding | tolerated(0.27) | benign(0.017) | TCGA-A7-A13E-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Targeted Molecular therapy | bevacizumab | PD | |
XPO5 | SNV | Missense_Mutation | novel | c.200G>C | p.Gly67Ala | p.G67A | Q9HAV4 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-A7-A56D-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD |
XPO5 | SNV | Missense_Mutation | c.3592N>A | p.Leu1198Met | p.L1198M | Q9HAV4 | protein_coding | deleterious(0.01) | possibly_damaging(0.786) | TCGA-A8-A08R-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
XPO5 | SNV | Missense_Mutation | c.2624C>T | p.Ser875Leu | p.S875L | Q9HAV4 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
XPO5 | SNV | Missense_Mutation | novel | c.1793N>T | p.Arg598Met | p.R598M | Q9HAV4 | protein_coding | tolerated(0.18) | benign(0.006) | TCGA-AN-A0FX-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
XPO5 | SNV | Missense_Mutation | c.346C>G | p.Leu116Val | p.L116V | Q9HAV4 | protein_coding | tolerated(0.26) | possibly_damaging(0.622) | TCGA-BH-A0EA-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | taxotere | CR | |
XPO5 | SNV | Missense_Mutation | c.1906N>C | p.Asn636His | p.N636H | Q9HAV4 | protein_coding | deleterious(0.02) | possibly_damaging(0.592) | TCGA-D8-A1XQ-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
XPO5 | SNV | Missense_Mutation | novel | c.1106N>A | p.Ser369Tyr | p.S369Y | Q9HAV4 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-D8-A73U-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | 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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