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Gene: NAGLU |
Gene summary for NAGLU |
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Gene information | Species | Human | Gene symbol | NAGLU | Gene ID | 4669 |
Gene name | N-acetyl-alpha-glucosaminidase | |
Gene Alias | CMT2V | |
Cytomap | 17q21.2 | |
Gene Type | protein-coding | GO ID | GO:0001654 | UniProtAcc | A0A140VJE4 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
4669 | NAGLU | HCC1_Meng | Human | Liver | HCC | 6.46e-61 | 2.00e-01 | 0.0246 |
4669 | NAGLU | HCC2_Meng | Human | Liver | HCC | 8.31e-16 | 1.44e-01 | 0.0107 |
4669 | NAGLU | HCC2 | Human | Liver | HCC | 7.73e-04 | 1.53e+00 | 0.5341 |
4669 | NAGLU | Pt13.b | Human | Liver | HCC | 2.19e-04 | 1.41e-01 | 0.0251 |
4669 | NAGLU | S014 | Human | Liver | HCC | 2.72e-02 | 2.31e-01 | 0.2254 |
4669 | NAGLU | S015 | Human | Liver | HCC | 8.73e-03 | 2.77e-01 | 0.2375 |
4669 | NAGLU | S016 | Human | Liver | HCC | 3.30e-06 | 2.64e-01 | 0.2243 |
4669 | NAGLU | S027 | Human | Liver | HCC | 6.59e-04 | 4.85e-01 | 0.2446 |
4669 | NAGLU | S028 | Human | Liver | HCC | 6.41e-22 | 6.21e-01 | 0.2503 |
4669 | NAGLU | S029 | Human | Liver | HCC | 1.78e-12 | 5.34e-01 | 0.2581 |
4669 | NAGLU | C04 | Human | Oral cavity | OSCC | 1.88e-04 | 2.57e-01 | 0.2633 |
4669 | NAGLU | C21 | Human | Oral cavity | OSCC | 1.15e-06 | 1.90e-01 | 0.2678 |
4669 | NAGLU | C30 | Human | Oral cavity | OSCC | 7.73e-28 | 1.31e+00 | 0.3055 |
4669 | NAGLU | C51 | Human | Oral cavity | OSCC | 1.08e-08 | 5.45e-01 | 0.2674 |
4669 | NAGLU | C06 | Human | Oral cavity | OSCC | 4.46e-02 | 5.45e-01 | 0.2699 |
4669 | NAGLU | C08 | Human | Oral cavity | OSCC | 1.27e-16 | 3.44e-01 | 0.1919 |
4669 | NAGLU | LN46 | Human | Oral cavity | OSCC | 8.33e-06 | 2.80e-01 | 0.1666 |
4669 | NAGLU | SYSMH1 | Human | Oral cavity | OSCC | 8.86e-14 | 2.71e-01 | 0.1127 |
4669 | NAGLU | SYSMH2 | Human | Oral cavity | OSCC | 3.86e-20 | 3.91e-01 | 0.2326 |
4669 | NAGLU | SYSMH3 | Human | Oral cavity | OSCC | 1.43e-15 | 3.41e-01 | 0.2442 |
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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:000703311 | Liver | HCC | vacuole organization | 119/7958 | 180/18723 | 1.22e-10 | 4.25e-09 | 119 |
GO:000762321 | Liver | HCC | circadian rhythm | 117/7958 | 210/18723 | 7.29e-05 | 6.54e-04 | 117 |
GO:1901136 | Liver | HCC | carbohydrate derivative catabolic process | 98/7958 | 172/18723 | 8.71e-05 | 7.62e-04 | 98 |
GO:00070401 | Liver | HCC | lysosome organization | 47/7958 | 74/18723 | 2.13e-04 | 1.63e-03 | 47 |
GO:00801711 | Liver | HCC | lytic vacuole organization | 47/7958 | 74/18723 | 2.13e-04 | 1.63e-03 | 47 |
GO:004851121 | Liver | HCC | rhythmic process | 156/7958 | 298/18723 | 3.54e-04 | 2.46e-03 | 156 |
GO:00070335 | Oral cavity | OSCC | vacuole organization | 115/7305 | 180/18723 | 1.11e-11 | 4.00e-10 | 115 |
GO:00070402 | Oral cavity | OSCC | lysosome organization | 51/7305 | 74/18723 | 1.77e-07 | 2.87e-06 | 51 |
GO:00801712 | Oral cavity | OSCC | lytic vacuole organization | 51/7305 | 74/18723 | 1.77e-07 | 2.87e-06 | 51 |
GO:004851116 | Oral cavity | OSCC | rhythmic process | 157/7305 | 298/18723 | 1.00e-06 | 1.36e-05 | 157 |
GO:000762316 | Oral cavity | OSCC | circadian rhythm | 110/7305 | 210/18723 | 5.40e-05 | 4.48e-04 | 110 |
GO:19011361 | Oral cavity | OSCC | carbohydrate derivative catabolic process | 89/7305 | 172/18723 | 4.52e-04 | 2.73e-03 | 89 |
GO:000703315 | Thyroid | PTC | vacuole organization | 96/5968 | 180/18723 | 1.80e-09 | 5.13e-08 | 96 |
GO:0048511111 | Thyroid | PTC | rhythmic process | 131/5968 | 298/18723 | 7.06e-06 | 8.33e-05 | 131 |
GO:0007623111 | Thyroid | PTC | circadian rhythm | 96/5968 | 210/18723 | 1.74e-05 | 1.82e-04 | 96 |
GO:00070405 | Thyroid | PTC | lysosome organization | 38/5968 | 74/18723 | 3.84e-04 | 2.58e-03 | 38 |
GO:00801715 | Thyroid | PTC | lytic vacuole organization | 38/5968 | 74/18723 | 3.84e-04 | 2.58e-03 | 38 |
GO:000703322 | Thyroid | ATC | vacuole organization | 100/6293 | 180/18723 | 1.07e-09 | 2.71e-08 | 100 |
GO:004851124 | Thyroid | ATC | rhythmic process | 141/6293 | 298/18723 | 5.58e-07 | 7.93e-06 | 141 |
GO:000762325 | Thyroid | ATC | circadian rhythm | 100/6293 | 210/18723 | 1.67e-05 | 1.54e-04 | 100 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa041422 | Liver | HCC | Lysosome | 100/4020 | 132/8465 | 2.32e-11 | 4.31e-10 | 2.40e-10 | 100 |
hsa041423 | Liver | HCC | Lysosome | 100/4020 | 132/8465 | 2.32e-11 | 4.31e-10 | 2.40e-10 | 100 |
hsa041425 | Oral cavity | OSCC | Lysosome | 87/3704 | 132/8465 | 1.97e-07 | 1.35e-06 | 6.86e-07 | 87 |
hsa0414212 | Oral cavity | OSCC | Lysosome | 87/3704 | 132/8465 | 1.97e-07 | 1.35e-06 | 6.86e-07 | 87 |
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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 |
NAGLU | SNV | Missense_Mutation | c.660C>G | p.Ile220Met | p.I220M | P54802 | protein_coding | tolerated(0.14) | benign(0.078) | TCGA-IR-A3LH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
NAGLU | SNV | Missense_Mutation | rs104894597 | c.1693C>T | p.Arg565Trp | p.R565W | P54802 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-VS-A9UH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
NAGLU | SNV | Missense_Mutation | rs752264680 | c.593N>A | p.Phe198Tyr | p.F198Y | P54802 | protein_coding | deleterious(0.01) | benign(0.347) | TCGA-A6-6140-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Chemotherapy | oxaliplatin | SD |
NAGLU | SNV | Missense_Mutation | c.446N>A | p.Arg149His | p.R149H | P54802 | protein_coding | deleterious(0.02) | probably_damaging(0.983) | TCGA-A6-6653-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
NAGLU | SNV | Missense_Mutation | rs749140168 | c.1000G>A | p.Val334Ile | p.V334I | P54802 | protein_coding | tolerated(0.22) | benign(0.228) | TCGA-AA-3715-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
NAGLU | SNV | Missense_Mutation | novel | c.1129C>A | p.Arg377Ser | p.R377S | P54802 | protein_coding | deleterious(0.02) | possibly_damaging(0.891) | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
NAGLU | SNV | Missense_Mutation | c.1019N>A | p.Ala340Glu | p.A340E | P54802 | protein_coding | tolerated(0.34) | benign(0.01) | TCGA-AA-A024-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
NAGLU | SNV | Missense_Mutation | c.1235N>A | p.Gly412Glu | p.G412E | P54802 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AY-6197-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
NAGLU | SNV | Missense_Mutation | rs773054539 | c.1547C>T | p.Pro516Leu | p.P516L | P54802 | protein_coding | tolerated(0.72) | possibly_damaging(0.874) | TCGA-CK-4951-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
NAGLU | SNV | Missense_Mutation | rs760257524 | c.2057T>C | p.Val686Ala | p.V686A | P54802 | protein_coding | deleterious(0) | benign(0.084) | TCGA-CK-5916-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
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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 |
4669 | NAGLU | ENZYME, DRUGGABLE GENOME | N-Acetyl-D-glucosamine |
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