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Gene: ELL |
Gene summary for ELL |
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Gene information | Species | Human | Gene symbol | ELL | Gene ID | 8178 |
Gene name | elongation factor for RNA polymerase II | |
Gene Alias | C19orf17 | |
Cytomap | 19p13.11 | |
Gene Type | protein-coding | GO ID | GO:0001701 | UniProtAcc | P55199 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
8178 | ELL | LZE4T | Human | Esophagus | ESCC | 2.00e-04 | 1.07e-01 | 0.0811 |
8178 | ELL | LZE7T | Human | Esophagus | ESCC | 1.56e-02 | 1.26e-01 | 0.0667 |
8178 | ELL | LZE20T | Human | Esophagus | ESCC | 2.13e-03 | 4.79e-02 | 0.0662 |
8178 | ELL | LZE24T | Human | Esophagus | ESCC | 9.26e-15 | 3.33e-01 | 0.0596 |
8178 | ELL | P1T-E | Human | Esophagus | ESCC | 1.26e-05 | 3.74e-01 | 0.0875 |
8178 | ELL | P2T-E | Human | Esophagus | ESCC | 1.39e-10 | 4.83e-02 | 0.1177 |
8178 | ELL | P4T-E | Human | Esophagus | ESCC | 7.54e-04 | 1.04e-01 | 0.1323 |
8178 | ELL | P5T-E | Human | Esophagus | ESCC | 9.45e-15 | 1.26e-01 | 0.1327 |
8178 | ELL | P8T-E | Human | Esophagus | ESCC | 8.67e-11 | 1.31e-01 | 0.0889 |
8178 | ELL | P9T-E | Human | Esophagus | ESCC | 1.00e-15 | 2.80e-01 | 0.1131 |
8178 | ELL | P10T-E | Human | Esophagus | ESCC | 1.32e-16 | 1.32e-01 | 0.116 |
8178 | ELL | P11T-E | Human | Esophagus | ESCC | 8.82e-07 | 4.68e-01 | 0.1426 |
8178 | ELL | P12T-E | Human | Esophagus | ESCC | 1.78e-12 | 2.78e-01 | 0.1122 |
8178 | ELL | P15T-E | Human | Esophagus | ESCC | 2.00e-16 | 2.20e-01 | 0.1149 |
8178 | ELL | P16T-E | Human | Esophagus | ESCC | 8.39e-05 | 7.27e-03 | 0.1153 |
8178 | ELL | P17T-E | Human | Esophagus | ESCC | 2.22e-05 | 2.24e-01 | 0.1278 |
8178 | ELL | P19T-E | Human | Esophagus | ESCC | 7.27e-03 | 1.77e-01 | 0.1662 |
8178 | ELL | P20T-E | Human | Esophagus | ESCC | 1.75e-11 | 2.80e-01 | 0.1124 |
8178 | ELL | P21T-E | Human | Esophagus | ESCC | 6.19e-19 | 3.68e-01 | 0.1617 |
8178 | ELL | P22T-E | Human | Esophagus | ESCC | 6.17e-15 | 6.82e-02 | 0.1236 |
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Tissue | Expression Dynamics | Abbreviation |
Esophagus | ![]() | ESCC: Esophageal squamous cell carcinoma |
HGIN: High-grade intraepithelial neoplasias | ||
LGIN: Low-grade intraepithelial neoplasias |
∗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:00063684 | Cervix | CC | transcription elongation from RNA polymerase II promoter | 17/2311 | 69/18723 | 3.65e-03 | 2.33e-02 | 17 |
GO:00063545 | Cervix | CC | DNA-templated transcription, elongation | 20/2311 | 91/18723 | 6.88e-03 | 3.74e-02 | 20 |
GO:0006354 | Colorectum | AD | DNA-templated transcription, elongation | 31/3918 | 91/18723 | 2.46e-03 | 1.90e-02 | 31 |
GO:0006368 | Colorectum | AD | transcription elongation from RNA polymerase II promoter | 24/3918 | 69/18723 | 5.35e-03 | 3.52e-02 | 24 |
GO:00063541 | Colorectum | MSS | DNA-templated transcription, elongation | 29/3467 | 91/18723 | 1.52e-03 | 1.39e-02 | 29 |
GO:00063681 | Colorectum | MSS | transcription elongation from RNA polymerase II promoter | 22/3467 | 69/18723 | 5.31e-03 | 3.62e-02 | 22 |
GO:00063682 | Colorectum | FAP | transcription elongation from RNA polymerase II promoter | 20/2622 | 69/18723 | 9.25e-04 | 9.26e-03 | 20 |
GO:00063542 | Colorectum | FAP | DNA-templated transcription, elongation | 24/2622 | 91/18723 | 1.32e-03 | 1.22e-02 | 24 |
GO:00063543 | Colorectum | CRC | DNA-templated transcription, elongation | 19/2078 | 91/18723 | 4.74e-03 | 3.67e-02 | 19 |
GO:00514039 | Endometrium | AEH | stress-activated MAPK cascade | 50/2100 | 239/18723 | 9.33e-06 | 2.18e-04 | 50 |
GO:00310989 | Endometrium | AEH | stress-activated protein kinase signaling cascade | 51/2100 | 247/18723 | 1.12e-05 | 2.52e-04 | 51 |
GO:00328728 | Endometrium | AEH | regulation of stress-activated MAPK cascade | 42/2100 | 192/18723 | 1.53e-05 | 3.23e-04 | 42 |
GO:00380665 | Endometrium | AEH | p38MAPK cascade | 18/2100 | 55/18723 | 1.77e-05 | 3.65e-04 | 18 |
GO:00434105 | Endometrium | AEH | positive regulation of MAPK cascade | 84/2100 | 480/18723 | 2.19e-05 | 4.25e-04 | 84 |
GO:00703028 | Endometrium | AEH | regulation of stress-activated protein kinase signaling cascade | 42/2100 | 195/18723 | 2.27e-05 | 4.35e-04 | 42 |
GO:19007443 | Endometrium | AEH | regulation of p38MAPK cascade | 15/2100 | 47/18723 | 1.21e-04 | 1.67e-03 | 15 |
GO:19007452 | Endometrium | AEH | positive regulation of p38MAPK cascade | 10/2100 | 32/18723 | 1.94e-03 | 1.52e-02 | 10 |
GO:00328743 | Endometrium | AEH | positive regulation of stress-activated MAPK cascade | 25/2100 | 126/18723 | 3.18e-03 | 2.24e-02 | 25 |
GO:00703044 | Endometrium | AEH | positive regulation of stress-activated protein kinase signaling cascade | 25/2100 | 128/18723 | 3.95e-03 | 2.65e-02 | 25 |
GO:003806612 | Endometrium | EEC | p38MAPK cascade | 21/2168 | 55/18723 | 3.30e-07 | 1.33e-05 | 21 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa032509 | Esophagus | ESCC | Viral life cycle - HIV-1 | 54/4205 | 63/8465 | 2.01e-09 | 2.17e-08 | 1.11e-08 | 54 |
hsa0325014 | Esophagus | ESCC | Viral life cycle - HIV-1 | 54/4205 | 63/8465 | 2.01e-09 | 2.17e-08 | 1.11e-08 | 54 |
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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 |
ELL | SNV | Missense_Mutation | novel | c.755N>C | p.Met252Thr | p.M252T | P55199 | protein_coding | deleterious(0.01) | benign(0.015) | TCGA-FI-A2D5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatinum | PD |
ELL | deletion | Frame_Shift_Del | novel | c.932delN | p.Pro311GlnfsTer24 | p.P311Qfs*24 | P55199 | protein_coding | TCGA-AJ-A2QO-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
ELL | SNV | Missense_Mutation | c.259G>A | p.Asp87Asn | p.D87N | P55199 | protein_coding | tolerated(0.05) | probably_damaging(0.999) | TCGA-DD-A3A9-01 | Liver | liver hepatocellular carcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
ELL | SNV | Missense_Mutation | novel | c.1065N>T | p.Lys355Asn | p.K355N | P55199 | protein_coding | deleterious(0.04) | possibly_damaging(0.638) | TCGA-95-7043-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
ELL | SNV | Missense_Mutation | c.1828N>A | p.Ala610Thr | p.A610T | P55199 | protein_coding | deleterious(0.01) | probably_damaging(0.992) | TCGA-18-3412-01 | Lung | lung squamous cell carcinoma | Male | <65 | I/II | Chemotherapy | vinorelbine | PD | |
ELL | SNV | Missense_Mutation | rs138181189 | c.1334N>A | p.Arg445His | p.R445H | P55199 | protein_coding | tolerated(0.59) | benign(0) | TCGA-39-5019-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
ELL | SNV | Missense_Mutation | novel | c.37T>C | p.Ser13Pro | p.S13P | P55199 | protein_coding | deleterious(0.01) | probably_damaging(0.997) | TCGA-CV-7422-01 | Oral cavity | head & neck squamous cell carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
ELL | SNV | Missense_Mutation | c.869N>A | p.Arg290Gln | p.R290Q | P55199 | protein_coding | deleterious(0.01) | probably_damaging(0.998) | TCGA-BR-A4QL-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | xeloda | CR | |
ELL | SNV | Missense_Mutation | rs142055049 | c.1517C>T | p.Thr506Met | p.T506M | P55199 | protein_coding | tolerated(0.32) | benign(0.009) | TCGA-HU-A4G9-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ELL | SNV | Missense_Mutation | c.1196N>G | p.Asp399Gly | p.D399G | P55199 | protein_coding | deleterious(0.04) | benign(0.011) | TCGA-HU-A4GT-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Chemotherapy | copolang | 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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