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Gene: ITGAE |
Gene summary for ITGAE |
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Gene information | Species | Human | Gene symbol | ITGAE | Gene ID | 3682 |
Gene name | integrin subunit alpha E | |
Gene Alias | CD103 | |
Cytomap | 17p13.2 | |
Gene Type | protein-coding | GO ID | GO:0007154 | UniProtAcc | P38570 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
3682 | ITGAE | LZE2T | Human | Esophagus | ESCC | 6.90e-04 | 9.40e-01 | 0.082 |
3682 | ITGAE | LZE4T | Human | Esophagus | ESCC | 3.52e-18 | 8.38e-01 | 0.0811 |
3682 | ITGAE | LZE7T | Human | Esophagus | ESCC | 1.08e-10 | 8.42e-01 | 0.0667 |
3682 | ITGAE | LZE8T | Human | Esophagus | ESCC | 9.92e-09 | 4.83e-01 | 0.067 |
3682 | ITGAE | LZE20T | Human | Esophagus | ESCC | 1.24e-02 | 9.21e-02 | 0.0662 |
3682 | ITGAE | LZE22D1 | Human | Esophagus | HGIN | 9.26e-03 | 1.11e-01 | 0.0595 |
3682 | ITGAE | LZE22T | Human | Esophagus | ESCC | 5.24e-04 | 3.14e-01 | 0.068 |
3682 | ITGAE | LZE24T | Human | Esophagus | ESCC | 1.57e-07 | 4.07e-01 | 0.0596 |
3682 | ITGAE | LZE21T | Human | Esophagus | ESCC | 3.84e-04 | 3.43e-01 | 0.0655 |
3682 | ITGAE | LZE6T | Human | Esophagus | ESCC | 4.00e-14 | 1.02e+00 | 0.0845 |
3682 | ITGAE | P1T-E | Human | Esophagus | ESCC | 2.97e-06 | 6.23e-01 | 0.0875 |
3682 | ITGAE | P2T-E | Human | Esophagus | ESCC | 3.85e-24 | 6.38e-01 | 0.1177 |
3682 | ITGAE | P4T-E | Human | Esophagus | ESCC | 2.62e-33 | 1.14e+00 | 0.1323 |
3682 | ITGAE | P5T-E | Human | Esophagus | ESCC | 1.27e-04 | 1.43e-01 | 0.1327 |
3682 | ITGAE | P8T-E | Human | Esophagus | ESCC | 6.11e-23 | 5.77e-01 | 0.0889 |
3682 | ITGAE | P9T-E | Human | Esophagus | ESCC | 6.09e-14 | 3.79e-01 | 0.1131 |
3682 | ITGAE | P10T-E | Human | Esophagus | ESCC | 5.08e-51 | 8.59e-01 | 0.116 |
3682 | ITGAE | P11T-E | Human | Esophagus | ESCC | 1.51e-10 | 7.48e-01 | 0.1426 |
3682 | ITGAE | P12T-E | Human | Esophagus | ESCC | 6.15e-35 | 7.92e-01 | 0.1122 |
3682 | ITGAE | P15T-E | Human | Esophagus | ESCC | 4.54e-11 | 3.07e-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:00072299 | Esophagus | ESCC | integrin-mediated signaling pathway | 67/8552 | 107/18723 | 3.03e-04 | 1.81e-03 | 67 |
GO:000722911 | Liver | Cirrhotic | integrin-mediated signaling pathway | 46/4634 | 107/18723 | 2.66e-05 | 3.42e-04 | 46 |
GO:00072292 | Liver | HCC | integrin-mediated signaling pathway | 60/7958 | 107/18723 | 3.15e-03 | 1.46e-02 | 60 |
GO:00072298 | Oral cavity | OSCC | integrin-mediated signaling pathway | 58/7305 | 107/18723 | 1.00e-03 | 5.20e-03 | 58 |
GO:000722916 | Oral cavity | LP | integrin-mediated signaling pathway | 42/4623 | 107/18723 | 5.96e-04 | 5.46e-03 | 42 |
GO:000722924 | Skin | cSCC | integrin-mediated signaling pathway | 47/4864 | 107/18723 | 4.21e-05 | 4.43e-04 | 47 |
GO:000722918 | Thyroid | PTC | integrin-mediated signaling pathway | 55/5968 | 107/18723 | 2.07e-05 | 2.08e-04 | 55 |
GO:000722919 | Thyroid | ATC | integrin-mediated signaling pathway | 63/6293 | 107/18723 | 7.09e-08 | 1.24e-06 | 63 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa0481028 | Esophagus | ESCC | Regulation of actin cytoskeleton | 133/4205 | 229/8465 | 5.94e-03 | 1.48e-02 | 7.56e-03 | 133 |
hsa04810112 | Esophagus | ESCC | Regulation of actin cytoskeleton | 133/4205 | 229/8465 | 5.94e-03 | 1.48e-02 | 7.56e-03 | 133 |
hsa0481021 | Liver | Cirrhotic | Regulation of actin cytoskeleton | 100/2530 | 229/8465 | 5.28e-06 | 5.50e-05 | 3.39e-05 | 100 |
hsa0481031 | Liver | Cirrhotic | Regulation of actin cytoskeleton | 100/2530 | 229/8465 | 5.28e-06 | 5.50e-05 | 3.39e-05 | 100 |
hsa0481041 | Liver | HCC | Regulation of actin cytoskeleton | 134/4020 | 229/8465 | 4.48e-04 | 1.94e-03 | 1.08e-03 | 134 |
hsa0481051 | Liver | HCC | Regulation of actin cytoskeleton | 134/4020 | 229/8465 | 4.48e-04 | 1.94e-03 | 1.08e-03 | 134 |
hsa0481026 | Oral cavity | OSCC | Regulation of actin cytoskeleton | 129/3704 | 229/8465 | 7.14e-05 | 2.74e-04 | 1.40e-04 | 129 |
hsa04810111 | Oral cavity | OSCC | Regulation of actin cytoskeleton | 129/3704 | 229/8465 | 7.14e-05 | 2.74e-04 | 1.40e-04 | 129 |
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Cell-cell communication analysis |
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Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Breast | DCIS |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Breast | Healthy |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Cervix | Precancer |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Endometrium | AEH |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Endometrium | Healthy |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | HNSCC | OSCC |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | HNSCC | Precancer |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Liver | HCC |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Liver | Precancer |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Prostate | BPH |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Prostate | Tumor |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Skin | ADJ |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | Skin | cSCC |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | THCA | Cancer |
CDH1 | ITGAE_ITGB7 | CDH1_ITGAE_ITGB7 | CDH1 | THCA | PTC |
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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 |
ITGAE | SNV | Missense_Mutation | rs768639646 | c.2515N>A | p.Val839Ile | p.V839I | P38570 | protein_coding | tolerated(1) | benign(0) | TCGA-FU-A3HZ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
ITGAE | SNV | Missense_Mutation | novel | c.3287N>G | p.Asn1096Ser | p.N1096S | P38570 | protein_coding | tolerated(0.05) | benign(0.396) | TCGA-A6-2672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
ITGAE | SNV | Missense_Mutation | rs777253108 | c.1870N>A | p.Gly624Ser | p.G624S | P38570 | protein_coding | tolerated(0.15) | benign(0.289) | TCGA-A6-2679-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ITGAE | SNV | Missense_Mutation | c.1410N>T | p.Lys470Asn | p.K470N | P38570 | protein_coding | tolerated(0.29) | benign(0.003) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
ITGAE | SNV | Missense_Mutation | rs143859925 | c.769N>T | p.Arg257Trp | p.R257W | P38570 | protein_coding | deleterious(0.01) | possibly_damaging(0.761) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
ITGAE | SNV | Missense_Mutation | rs754058055 | c.1399G>A | p.Val467Met | p.V467M | P38570 | protein_coding | deleterious(0.04) | benign(0.421) | TCGA-AA-3710-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
ITGAE | SNV | Missense_Mutation | c.3247N>T | p.Asp1083Tyr | p.D1083Y | P38570 | protein_coding | deleterious(0) | probably_damaging(0.947) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
ITGAE | SNV | Missense_Mutation | c.472N>T | p.Asp158Tyr | p.D158Y | P38570 | protein_coding | deleterious(0.03) | possibly_damaging(0.483) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
ITGAE | SNV | Missense_Mutation | rs757934661 | c.1889N>T | p.Ser630Leu | p.S630L | P38570 | protein_coding | deleterious(0.01) | possibly_damaging(0.734) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
ITGAE | SNV | Missense_Mutation | novel | c.2993T>G | p.Leu998Arg | p.L998R | P38570 | protein_coding | tolerated(0.78) | benign(0.005) | TCGA-AA-A01K-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Chemotherapy | folinic | CR |
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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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