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Gene: NPRL3 |
Gene summary for NPRL3 |
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Gene information | Species | Human | Gene symbol | NPRL3 | Gene ID | 8131 |
Gene name | NPR3 like, GATOR1 complex subunit | |
Gene Alias | C16orf35 | |
Cytomap | 16p13.3 | |
Gene Type | protein-coding | GO ID | GO:0000045 | UniProtAcc | Q9BTE2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
8131 | NPRL3 | LZE7T | Human | Esophagus | ESCC | 1.31e-08 | 2.80e-01 | 0.0667 |
8131 | NPRL3 | LZE8T | Human | Esophagus | ESCC | 7.37e-05 | 8.45e-02 | 0.067 |
8131 | NPRL3 | LZE22T | Human | Esophagus | ESCC | 2.42e-07 | 3.69e-01 | 0.068 |
8131 | NPRL3 | LZE24T | Human | Esophagus | ESCC | 9.57e-08 | 2.07e-01 | 0.0596 |
8131 | NPRL3 | LZE21T | Human | Esophagus | ESCC | 4.50e-02 | 1.11e-01 | 0.0655 |
8131 | NPRL3 | P1T-E | Human | Esophagus | ESCC | 2.02e-02 | 2.77e-01 | 0.0875 |
8131 | NPRL3 | P2T-E | Human | Esophagus | ESCC | 2.57e-25 | 5.10e-01 | 0.1177 |
8131 | NPRL3 | P4T-E | Human | Esophagus | ESCC | 2.18e-06 | 6.48e-02 | 0.1323 |
8131 | NPRL3 | P5T-E | Human | Esophagus | ESCC | 5.06e-14 | 1.47e-01 | 0.1327 |
8131 | NPRL3 | P8T-E | Human | Esophagus | ESCC | 6.14e-13 | 2.30e-01 | 0.0889 |
8131 | NPRL3 | P9T-E | Human | Esophagus | ESCC | 1.68e-07 | 7.77e-02 | 0.1131 |
8131 | NPRL3 | P10T-E | Human | Esophagus | ESCC | 5.38e-13 | 2.28e-01 | 0.116 |
8131 | NPRL3 | P11T-E | Human | Esophagus | ESCC | 9.08e-03 | 1.06e-01 | 0.1426 |
8131 | NPRL3 | P12T-E | Human | Esophagus | ESCC | 3.22e-17 | 3.57e-01 | 0.1122 |
8131 | NPRL3 | P15T-E | Human | Esophagus | ESCC | 1.97e-14 | 2.44e-01 | 0.1149 |
8131 | NPRL3 | P16T-E | Human | Esophagus | ESCC | 6.34e-13 | 1.58e-01 | 0.1153 |
8131 | NPRL3 | P17T-E | Human | Esophagus | ESCC | 4.03e-04 | 2.28e-01 | 0.1278 |
8131 | NPRL3 | P20T-E | Human | Esophagus | ESCC | 9.65e-19 | 3.40e-01 | 0.1124 |
8131 | NPRL3 | P21T-E | Human | Esophagus | ESCC | 6.31e-13 | 1.43e-01 | 0.1617 |
8131 | NPRL3 | P22T-E | Human | Esophagus | ESCC | 3.01e-20 | 3.70e-01 | 0.1236 |
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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:001623617 | Esophagus | ESCC | macroautophagy | 216/8552 | 291/18723 | 1.94e-23 | 4.57e-21 | 216 |
GO:0071496111 | Esophagus | ESCC | cellular response to external stimulus | 215/8552 | 320/18723 | 4.29e-15 | 2.43e-13 | 215 |
GO:0031668111 | Esophagus | ESCC | cellular response to extracellular stimulus | 168/8552 | 246/18723 | 4.93e-13 | 2.23e-11 | 168 |
GO:0031669110 | Esophagus | ESCC | cellular response to nutrient levels | 148/8552 | 215/18723 | 4.58e-12 | 1.76e-10 | 148 |
GO:0031667111 | Esophagus | ESCC | response to nutrient levels | 289/8552 | 474/18723 | 9.25e-12 | 3.47e-10 | 289 |
GO:000703314 | Esophagus | ESCC | vacuole organization | 127/8552 | 180/18723 | 1.04e-11 | 3.85e-10 | 127 |
GO:0009267110 | Esophagus | ESCC | cellular response to starvation | 110/8552 | 156/18723 | 2.63e-10 | 7.37e-09 | 110 |
GO:004259419 | Esophagus | ESCC | response to starvation | 133/8552 | 197/18723 | 4.31e-10 | 1.14e-08 | 133 |
GO:190503712 | Esophagus | ESCC | autophagosome organization | 73/8552 | 103/18723 | 1.88e-07 | 2.93e-06 | 73 |
GO:000004513 | Esophagus | ESCC | autophagosome assembly | 69/8552 | 99/18723 | 1.10e-06 | 1.38e-05 | 69 |
GO:190211514 | Esophagus | ESCC | regulation of organelle assembly | 116/8552 | 186/18723 | 3.15e-06 | 3.53e-05 | 116 |
GO:19909284 | Esophagus | ESCC | response to amino acid starvation | 37/8552 | 49/18723 | 2.05e-05 | 1.78e-04 | 37 |
GO:00319294 | Esophagus | ESCC | TOR signaling | 79/8552 | 126/18723 | 8.57e-05 | 6.21e-04 | 79 |
GO:00341984 | Esophagus | ESCC | cellular response to amino acid starvation | 34/8552 | 46/18723 | 9.39e-05 | 6.70e-04 | 34 |
GO:004408812 | Esophagus | ESCC | regulation of vacuole organization | 32/8552 | 45/18723 | 4.87e-04 | 2.70e-03 | 32 |
GO:00320061 | Esophagus | ESCC | regulation of TOR signaling | 63/8552 | 104/18723 | 1.55e-03 | 7.29e-03 | 63 |
GO:200078512 | Esophagus | ESCC | regulation of autophagosome assembly | 27/8552 | 39/18723 | 2.52e-03 | 1.08e-02 | 27 |
GO:006053716 | Esophagus | ESCC | muscle tissue development | 211/8552 | 403/18723 | 3.84e-03 | 1.56e-02 | 211 |
GO:0060021 | Esophagus | ESCC | roof of mouth development | 50/8552 | 85/18723 | 1.00e-02 | 3.42e-02 | 50 |
GO:001470615 | Esophagus | ESCC | striated muscle tissue development | 197/8552 | 384/18723 | 1.46e-02 | 4.74e-02 | 197 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa041505 | Esophagus | ESCC | mTOR signaling pathway | 98/4205 | 156/8465 | 5.81e-04 | 1.95e-03 | 9.97e-04 | 98 |
hsa0415013 | Esophagus | ESCC | mTOR signaling pathway | 98/4205 | 156/8465 | 5.81e-04 | 1.95e-03 | 9.97e-04 | 98 |
hsa041502 | Liver | HCC | mTOR signaling pathway | 95/4020 | 156/8465 | 4.70e-04 | 1.99e-03 | 1.11e-03 | 95 |
hsa0415011 | Liver | HCC | mTOR signaling pathway | 95/4020 | 156/8465 | 4.70e-04 | 1.99e-03 | 1.11e-03 | 95 |
hsa041504 | Oral cavity | OSCC | mTOR signaling pathway | 90/3704 | 156/8465 | 2.87e-04 | 9.15e-04 | 4.66e-04 | 90 |
hsa0415012 | Oral cavity | OSCC | mTOR signaling pathway | 90/3704 | 156/8465 | 2.87e-04 | 9.15e-04 | 4.66e-04 | 90 |
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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 |
NPRL3 | SNV | Missense_Mutation | rs778377009 | c.1462G>C | p.Ala488Pro | p.A488P | Q12980 | protein_coding | tolerated(0.13) | possibly_damaging(0.502) | TCGA-A2-A0CS-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | anastrozole | SD |
NPRL3 | SNV | Missense_Mutation | rs778377009 | c.1462N>C | p.Ala488Pro | p.A488P | Q12980 | protein_coding | tolerated(0.13) | possibly_damaging(0.502) | TCGA-A2-A1FW-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | cytoxan | SD |
NPRL3 | SNV | Missense_Mutation | c.548N>C | p.Gly183Ala | p.G183A | Q12980 | protein_coding | tolerated(1) | benign(0) | TCGA-D8-A27G-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
NPRL3 | SNV | Missense_Mutation | rs778377009 | c.1462N>C | p.Ala488Pro | p.A488P | Q12980 | protein_coding | tolerated(0.13) | possibly_damaging(0.502) | TCGA-E2-A150-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD |
NPRL3 | SNV | Missense_Mutation | rs556683821 | c.1198C>T | p.Arg400Cys | p.R400C | Q12980 | protein_coding | deleterious(0) | possibly_damaging(0.541) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
NPRL3 | SNV | Missense_Mutation | rs769327693 | c.1606N>T | p.Arg536Trp | p.R536W | Q12980 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-AA-3982-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD |
NPRL3 | SNV | Missense_Mutation | rs556232826 | c.641N>T | p.Ser214Leu | p.S214L | Q12980 | protein_coding | deleterious(0) | benign(0.06) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
NPRL3 | SNV | Missense_Mutation | c.801N>T | p.Glu267Asp | p.E267D | Q12980 | protein_coding | tolerated(0.15) | probably_damaging(0.989) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR | |
NPRL3 | SNV | Missense_Mutation | c.113A>T | p.Gln38Leu | p.Q38L | Q12980 | protein_coding | tolerated(0.37) | benign(0) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
NPRL3 | SNV | Missense_Mutation | novel | c.640N>C | p.Ser214Pro | p.S214P | Q12980 | protein_coding | deleterious(0) | benign(0.198) | TCGA-D5-6927-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | 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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