![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: LIME1 |
Gene summary for LIME1 |
![]() |
Gene information | Species | Human | Gene symbol | LIME1 | Gene ID | 54923 |
Gene name | Lck interacting transmembrane adaptor 1 | |
Gene Alias | LIME | |
Cytomap | 20q13.33 | |
Gene Type | protein-coding | GO ID | GO:0001932 | UniProtAcc | A0A087WT39 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
54923 | LIME1 | LZE3D | Human | Esophagus | HGIN | 6.21e-05 | 9.26e-01 | 0.0668 |
54923 | LIME1 | LZE4T | Human | Esophagus | ESCC | 5.68e-07 | 2.32e-01 | 0.0811 |
54923 | LIME1 | LZE7T | Human | Esophagus | ESCC | 6.28e-20 | 7.98e-01 | 0.0667 |
54923 | LIME1 | LZE8T | Human | Esophagus | ESCC | 1.35e-07 | 2.76e-01 | 0.067 |
54923 | LIME1 | LZE22D1 | Human | Esophagus | HGIN | 2.88e-06 | 4.10e-01 | 0.0595 |
54923 | LIME1 | LZE22T | Human | Esophagus | ESCC | 1.57e-03 | 3.08e-01 | 0.068 |
54923 | LIME1 | LZE24T | Human | Esophagus | ESCC | 2.14e-21 | 5.56e-01 | 0.0596 |
54923 | LIME1 | LZE22D3 | Human | Esophagus | HGIN | 3.01e-07 | 5.85e-01 | 0.0653 |
54923 | LIME1 | LZE6T | Human | Esophagus | ESCC | 1.71e-05 | 3.26e-01 | 0.0845 |
54923 | LIME1 | P1T-E | Human | Esophagus | ESCC | 7.11e-04 | 2.04e-01 | 0.0875 |
54923 | LIME1 | P2T-E | Human | Esophagus | ESCC | 4.40e-09 | 1.70e-01 | 0.1177 |
54923 | LIME1 | P4T-E | Human | Esophagus | ESCC | 1.36e-04 | 1.70e-01 | 0.1323 |
54923 | LIME1 | P8T-E | Human | Esophagus | ESCC | 3.97e-04 | 1.04e-01 | 0.0889 |
54923 | LIME1 | P10T-E | Human | Esophagus | ESCC | 8.08e-19 | 3.27e-01 | 0.116 |
54923 | LIME1 | P12T-E | Human | Esophagus | ESCC | 3.97e-04 | 1.19e-01 | 0.1122 |
54923 | LIME1 | P17T-E | Human | Esophagus | ESCC | 4.79e-04 | 2.38e-01 | 0.1278 |
54923 | LIME1 | P20T-E | Human | Esophagus | ESCC | 1.19e-07 | 2.02e-01 | 0.1124 |
54923 | LIME1 | P21T-E | Human | Esophagus | ESCC | 1.53e-19 | 3.67e-01 | 0.1617 |
54923 | LIME1 | P31T-E | Human | Esophagus | ESCC | 4.16e-22 | 3.31e-01 | 0.1251 |
54923 | LIME1 | P40T-E | Human | Esophagus | ESCC | 2.37e-02 | 1.31e-01 | 0.109 |
Page: 1 2 3 |
![]() |
∗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. |
Top |
Malignant transformation related pathway analysis |
![]() |
![]() |
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). |
Page: 1 2 3 4 5 6 7 8 9 |
![]() |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:004312220 | Esophagus | HGIN | regulation of I-kappaB kinase/NF-kappaB signaling | 63/2587 | 249/18723 | 8.91e-07 | 3.61e-05 | 63 |
GO:000724918 | Esophagus | HGIN | I-kappaB kinase/NF-kappaB signaling | 67/2587 | 281/18723 | 3.84e-06 | 1.29e-04 | 67 |
GO:005165126 | Esophagus | HGIN | maintenance of location in cell | 53/2587 | 214/18723 | 1.22e-05 | 3.45e-04 | 53 |
GO:005123520 | Esophagus | HGIN | maintenance of location | 73/2587 | 327/18723 | 1.73e-05 | 4.71e-04 | 73 |
GO:0043122110 | Esophagus | ESCC | regulation of I-kappaB kinase/NF-kappaB signaling | 167/8552 | 249/18723 | 6.11e-12 | 2.32e-10 | 167 |
GO:007190016 | Esophagus | ESCC | regulation of protein serine/threonine kinase activity | 227/8552 | 359/18723 | 1.12e-11 | 4.10e-10 | 227 |
GO:000724919 | Esophagus | ESCC | I-kappaB kinase/NF-kappaB signaling | 183/8552 | 281/18723 | 3.02e-11 | 1.01e-09 | 183 |
GO:0051235110 | Esophagus | ESCC | maintenance of location | 200/8552 | 327/18723 | 1.01e-08 | 2.02e-07 | 200 |
GO:0051651111 | Esophagus | ESCC | maintenance of location in cell | 126/8552 | 214/18723 | 6.57e-05 | 5.00e-04 | 126 |
GO:00434055 | Esophagus | ESCC | regulation of MAP kinase activity | 102/8552 | 177/18723 | 8.89e-04 | 4.55e-03 | 102 |
GO:00508528 | Esophagus | ESCC | T cell receptor signaling pathway | 73/8552 | 123/18723 | 1.54e-03 | 7.24e-03 | 73 |
GO:00380615 | Esophagus | ESCC | NIK/NF-kappaB signaling | 81/8552 | 143/18723 | 5.33e-03 | 2.00e-02 | 81 |
GO:005123521 | Liver | HCC | maintenance of location | 185/7958 | 327/18723 | 1.70e-07 | 3.12e-06 | 185 |
GO:000724912 | Liver | HCC | I-kappaB kinase/NF-kappaB signaling | 156/7958 | 281/18723 | 6.66e-06 | 8.00e-05 | 156 |
GO:004312212 | Liver | HCC | regulation of I-kappaB kinase/NF-kappaB signaling | 138/7958 | 249/18723 | 2.47e-05 | 2.58e-04 | 138 |
GO:007190021 | Liver | HCC | regulation of protein serine/threonine kinase activity | 189/7958 | 359/18723 | 5.97e-05 | 5.47e-04 | 189 |
GO:005165112 | Liver | HCC | maintenance of location in cell | 119/7958 | 214/18723 | 7.11e-05 | 6.39e-04 | 119 |
GO:00380611 | Liver | HCC | NIK/NF-kappaB signaling | 77/7958 | 143/18723 | 3.98e-03 | 1.76e-02 | 77 |
GO:19012221 | Liver | HCC | regulation of NIK/NF-kappaB signaling | 60/7958 | 112/18723 | 1.17e-02 | 4.28e-02 | 60 |
GO:0051235 | Stomach | GC | maintenance of location | 41/1159 | 327/18723 | 1.33e-05 | 4.35e-04 | 41 |
Page: 1 2 3 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
Top |
Cell-cell communication analysis |
![]() |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
![]() |
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. |
Page: 1 |
Top |
Somatic mutation of malignant transformation related genes |
![]() |
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 |
LIME1 | SNV | Missense_Mutation | c.580N>A | p.Ala194Thr | p.A194T | Q9H400 | protein_coding | tolerated(0.67) | benign(0.006) | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
LIME1 | SNV | Missense_Mutation | novel | c.445N>T | p.Gly149Trp | p.G149W | Q9H400 | protein_coding | deleterious(0.01) | probably_damaging(1) | TCGA-AJ-A3OJ-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
LIME1 | SNV | Missense_Mutation | novel | c.646G>T | p.Asp216Tyr | p.D216Y | Q9H400 | protein_coding | deleterious(0.01) | possibly_damaging(0.808) | TCGA-B5-A3FC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
LIME1 | SNV | Missense_Mutation | rs776251119 | c.716C>T | p.Pro239Leu | p.P239L | Q9H400 | protein_coding | deleterious(0.03) | benign(0.014) | TCGA-D1-A1NZ-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
LIME1 | SNV | Missense_Mutation | novel | c.517C>T | p.Arg173Cys | p.R173C | Q9H400 | protein_coding | tolerated(0.12) | possibly_damaging(0.735) | TCGA-FI-A2D0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
LIME1 | deletion | Frame_Shift_Del | novel | c.487delG | p.Val163TrpfsTer28 | p.V163Wfs*28 | Q9H400 | protein_coding | TCGA-DI-A1BU-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | paclitaxel | SD | ||
LIME1 | SNV | Missense_Mutation | c.127N>T | p.Arg43Trp | p.R43W | Q9H400 | protein_coding | deleterious(0.01) | benign(0.038) | TCGA-86-8358-01 | Lung | lung adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
LIME1 | SNV | Missense_Mutation | novel | c.86C>T | p.Thr29Ile | p.T29I | Q9H400 | protein_coding | deleterious(0) | possibly_damaging(0.744) | TCGA-NC-A5HG-01 | Lung | lung squamous cell carcinoma | Male | <65 | III/IV | Chemotherapy | cisplatin | CR |
LIME1 | SNV | Missense_Mutation | rs774768440 | c.592N>A | p.Val198Ile | p.V198I | Q9H400 | protein_coding | tolerated(1) | benign(0.003) | TCGA-BA-A6DI-01 | Oral cavity | head & neck squamous cell carcinoma | Male | <65 | I/II | Chemotherapy | cisplatin | PD |
LIME1 | SNV | Missense_Mutation | c.656N>G | p.Asp219Gly | p.D219G | Q9H400 | protein_coding | tolerated(0.11) | benign(0.003) | TCGA-EJ-A65M-01 | Prostate | prostate adenocarcinoma | Male | >=65 | 6 | Unknown | Unknown | SD |
Page: 1 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |