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Gene: NLE1 |
Gene summary for NLE1 |
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Gene information | Species | Human | Gene symbol | NLE1 | Gene ID | 54475 |
Gene name | notchless homolog 1 | |
Gene Alias | NLE | |
Cytomap | 17q12 | |
Gene Type | protein-coding | GO ID | GO:0000027 | UniProtAcc | Q9NVX2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
54475 | NLE1 | LZE4T | Human | Esophagus | ESCC | 4.95e-06 | 8.81e-02 | 0.0811 |
54475 | NLE1 | LZE7T | Human | Esophagus | ESCC | 1.99e-02 | 1.23e-01 | 0.0667 |
54475 | NLE1 | LZE24T | Human | Esophagus | ESCC | 2.91e-08 | 1.31e-01 | 0.0596 |
54475 | NLE1 | P1T-E | Human | Esophagus | ESCC | 1.55e-02 | 9.19e-02 | 0.0875 |
54475 | NLE1 | P2T-E | Human | Esophagus | ESCC | 2.20e-07 | 2.26e-01 | 0.1177 |
54475 | NLE1 | P4T-E | Human | Esophagus | ESCC | 7.47e-09 | 2.62e-01 | 0.1323 |
54475 | NLE1 | P5T-E | Human | Esophagus | ESCC | 1.35e-18 | 3.79e-01 | 0.1327 |
54475 | NLE1 | P8T-E | Human | Esophagus | ESCC | 2.30e-02 | 4.11e-02 | 0.0889 |
54475 | NLE1 | P9T-E | Human | Esophagus | ESCC | 1.43e-21 | 1.68e-01 | 0.1131 |
54475 | NLE1 | P10T-E | Human | Esophagus | ESCC | 5.04e-03 | 2.92e-02 | 0.116 |
54475 | NLE1 | P11T-E | Human | Esophagus | ESCC | 2.65e-03 | 1.39e-01 | 0.1426 |
54475 | NLE1 | P12T-E | Human | Esophagus | ESCC | 9.39e-18 | 3.54e-01 | 0.1122 |
54475 | NLE1 | P15T-E | Human | Esophagus | ESCC | 2.04e-16 | 3.52e-01 | 0.1149 |
54475 | NLE1 | P16T-E | Human | Esophagus | ESCC | 4.11e-16 | 2.97e-01 | 0.1153 |
54475 | NLE1 | P19T-E | Human | Esophagus | ESCC | 3.59e-07 | 4.09e-01 | 0.1662 |
54475 | NLE1 | P20T-E | Human | Esophagus | ESCC | 3.50e-13 | 2.93e-01 | 0.1124 |
54475 | NLE1 | P21T-E | Human | Esophagus | ESCC | 1.26e-13 | 3.64e-01 | 0.1617 |
54475 | NLE1 | P22T-E | Human | Esophagus | ESCC | 4.84e-17 | 2.82e-01 | 0.1236 |
54475 | NLE1 | P23T-E | Human | Esophagus | ESCC | 1.10e-06 | 1.17e-01 | 0.108 |
54475 | NLE1 | P24T-E | Human | Esophagus | ESCC | 3.32e-12 | 4.09e-01 | 0.1287 |
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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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:004227322 | Liver | HCC | ribosomal large subunit biogenesis | 64/7958 | 72/18723 | 2.31e-16 | 2.03e-14 | 64 |
GO:002261822 | Liver | HCC | ribonucleoprotein complex assembly | 153/7958 | 220/18723 | 3.44e-16 | 2.91e-14 | 153 |
GO:200123322 | Liver | HCC | regulation of apoptotic signaling pathway | 226/7958 | 356/18723 | 7.26e-16 | 5.68e-14 | 226 |
GO:200123412 | Liver | HCC | negative regulation of apoptotic signaling pathway | 145/7958 | 224/18723 | 1.33e-11 | 5.36e-10 | 145 |
GO:004225522 | Liver | HCC | ribosome assembly | 50/7958 | 61/18723 | 2.79e-10 | 9.50e-09 | 50 |
GO:000734611 | Liver | HCC | regulation of mitotic cell cycle | 255/7958 | 457/18723 | 4.96e-09 | 1.30e-07 | 255 |
GO:019873821 | Liver | HCC | cell-cell signaling by wnt | 247/7958 | 446/18723 | 2.11e-08 | 4.96e-07 | 247 |
GO:001605521 | Liver | HCC | Wnt signaling pathway | 245/7958 | 444/18723 | 3.68e-08 | 8.09e-07 | 245 |
GO:000170111 | Liver | HCC | in utero embryonic development | 204/7958 | 367/18723 | 2.44e-07 | 4.30e-06 | 204 |
GO:004328112 | Liver | HCC | regulation of cysteine-type endopeptidase activity involved in apoptotic process | 125/7958 | 209/18723 | 3.12e-07 | 5.42e-06 | 125 |
GO:200011612 | Liver | HCC | regulation of cysteine-type endopeptidase activity | 137/7958 | 235/18723 | 6.91e-07 | 1.08e-05 | 137 |
GO:005254722 | Liver | HCC | regulation of peptidase activity | 247/7958 | 461/18723 | 8.28e-07 | 1.27e-05 | 247 |
GO:004315412 | Liver | HCC | negative regulation of cysteine-type endopeptidase activity involved in apoptotic process | 54/7958 | 78/18723 | 1.61e-06 | 2.27e-05 | 54 |
GO:005254822 | Liver | HCC | regulation of endopeptidase activity | 230/7958 | 432/18723 | 3.58e-06 | 4.68e-05 | 230 |
GO:003011121 | Liver | HCC | regulation of Wnt signaling pathway | 180/7958 | 328/18723 | 3.62e-06 | 4.72e-05 | 180 |
GO:200011712 | Liver | HCC | negative regulation of cysteine-type endopeptidase activity | 57/7958 | 86/18723 | 7.14e-06 | 8.47e-05 | 57 |
GO:0045786 | Liver | HCC | negative regulation of cell cycle | 204/7958 | 385/18723 | 1.84e-05 | 1.99e-04 | 204 |
GO:004586122 | Liver | HCC | negative regulation of proteolysis | 186/7958 | 351/18723 | 4.19e-05 | 4.11e-04 | 186 |
GO:0045930 | Liver | HCC | negative regulation of mitotic cell cycle | 130/7958 | 235/18723 | 4.69e-05 | 4.50e-04 | 130 |
GO:006007021 | Liver | HCC | canonical Wnt signaling pathway | 162/7958 | 303/18723 | 7.00e-05 | 6.32e-04 | 162 |
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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 |
NLE1 | SNV | Missense_Mutation | c.919N>C | p.Glu307Gln | p.E307Q | Q9NVX2 | protein_coding | tolerated(0.05) | possibly_damaging(0.583) | TCGA-A8-A08L-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
NLE1 | insertion | Frame_Shift_Ins | novel | c.784_785insGGGATGGGGA | p.Ser262TrpfsTer18 | p.S262Wfs*18 | Q9NVX2 | protein_coding | TCGA-BH-A0B1-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | adriamycin | SD | ||
NLE1 | insertion | Nonsense_Mutation | novel | c.782_783insTTGTAATGACTGGTAATGATTAAAAATGGT | p.Tyr261_Ser262insCysAsnAspTrpTerTerLeuLysMetVal | p.Y261_S262insCNDW**LKMV | Q9NVX2 | protein_coding | TCGA-BH-A0B1-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | adriamycin | SD | ||
NLE1 | SNV | Missense_Mutation | rs372790802 | c.718N>T | p.Arg240Cys | p.R240C | Q9NVX2 | protein_coding | tolerated(0.15) | possibly_damaging(0.761) | TCGA-A6-6653-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
NLE1 | SNV | Missense_Mutation | c.905N>A | p.Arg302His | p.R302H | Q9NVX2 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AA-3672-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
NLE1 | SNV | Missense_Mutation | c.356N>A | p.Ser119Tyr | p.S119Y | Q9NVX2 | protein_coding | deleterious(0.02) | probably_damaging(0.999) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
NLE1 | SNV | Missense_Mutation | novel | c.1264N>G | p.Trp422Gly | p.W422G | Q9NVX2 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-AD-6895-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
NLE1 | SNV | Missense_Mutation | rs200560049 | c.1154G>A | p.Arg385His | p.R385H | Q9NVX2 | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-AM-5821-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NLE1 | SNV | Missense_Mutation | c.771C>G | p.Asp257Glu | p.D257E | Q9NVX2 | protein_coding | tolerated(1) | benign(0.073) | TCGA-G4-6588-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NLE1 | SNV | Missense_Mutation | rs750583113 | c.1366N>A | p.Ala456Thr | p.A456T | Q9NVX2 | protein_coding | deleterious(0.05) | probably_damaging(0.999) | TCGA-AG-A02N-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | 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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