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Gene: NAPB |
Gene summary for NAPB |
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Gene information | Species | Human | Gene symbol | NAPB | Gene ID | 63908 |
Gene name | NSF attachment protein beta | |
Gene Alias | SNAP-BETA | |
Cytomap | 20p11.21 | |
Gene Type | protein-coding | GO ID | GO:0001505 | UniProtAcc | A0A087WZQ7 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
63908 | NAPB | NAFLD1 | Human | Liver | NAFLD | 8.31e-06 | 4.15e-01 | -0.04 |
63908 | NAPB | HCC1_Meng | Human | Liver | HCC | 4.05e-12 | 3.45e-02 | 0.0246 |
63908 | NAPB | HCC2_Meng | Human | Liver | HCC | 1.33e-02 | 1.40e-02 | 0.0107 |
63908 | NAPB | S014 | Human | Liver | HCC | 9.76e-07 | 3.82e-01 | 0.2254 |
63908 | NAPB | S015 | Human | Liver | HCC | 7.63e-16 | 6.96e-01 | 0.2375 |
63908 | NAPB | S016 | Human | Liver | HCC | 3.79e-14 | 5.18e-01 | 0.2243 |
63908 | NAPB | S028 | Human | Liver | HCC | 1.99e-02 | 1.92e-01 | 0.2503 |
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Tissue | Expression Dynamics | Abbreviation |
Liver | ![]() | HCC: Hepatocellular carcinoma |
NAFLD: Non-alcoholic fatty liver disease |
∗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:00432547 | Liver | NAFLD | regulation of protein-containing complex assembly | 66/1882 | 428/18723 | 2.83e-04 | 4.53e-03 | 66 |
GO:002241112 | Liver | HCC | cellular component disassembly | 282/7958 | 443/18723 | 1.02e-19 | 1.38e-17 | 282 |
GO:004325422 | Liver | HCC | regulation of protein-containing complex assembly | 264/7958 | 428/18723 | 5.47e-16 | 4.39e-14 | 264 |
GO:003298411 | Liver | HCC | protein-containing complex disassembly | 138/7958 | 224/18723 | 5.59e-09 | 1.46e-07 | 138 |
GO:00436242 | Liver | HCC | cellular protein complex disassembly | 71/7958 | 136/18723 | 1.39e-02 | 4.95e-02 | 71 |
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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 |
NAPB | SNV | Missense_Mutation | c.427N>C | p.Glu143Gln | p.E143Q | protein_coding | deleterious(0.04) | possibly_damaging(0.877) | TCGA-IR-A3LH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | ||
NAPB | SNV | Missense_Mutation | c.86N>A | p.Arg29Gln | p.R29Q | protein_coding | deleterious(0.03) | benign(0.065) | TCGA-IR-A3LH-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | ||
NAPB | SNV | Missense_Mutation | novel | c.325A>C | p.Asn109His | p.N109H | protein_coding | tolerated(0.13) | benign(0.393) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
NAPB | SNV | Missense_Mutation | c.799G>A | p.Val267Met | p.V267M | protein_coding | deleterious(0) | benign(0.382) | TCGA-AA-A01P-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | ||
NAPB | SNV | Missense_Mutation | c.896N>A | p.Gly299Glu | p.G299E | protein_coding | tolerated(0.37) | probably_damaging(1) | TCGA-NH-A6GC-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Chemotherapy | fluorouracil | SD | ||
NAPB | deletion | Frame_Shift_Del | c.170delA | p.Asn57IlefsTer52 | p.N57Ifs*52 | protein_coding | TCGA-AU-6004-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||||
NAPB | deletion | Frame_Shift_Del | c.293delA | p.Lys98ArgfsTer11 | p.K98Rfs*11 | protein_coding | TCGA-DM-A1HB-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | ||||
NAPB | SNV | Missense_Mutation | novel | c.158N>G | p.Lys53Arg | p.K53R | protein_coding | deleterious(0) | possibly_damaging(0.69) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NAPB | SNV | Missense_Mutation | novel | c.778N>G | p.Ser260Gly | p.S260G | protein_coding | tolerated(0.05) | benign(0) | TCGA-AJ-A3EL-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
NAPB | SNV | Missense_Mutation | novel | c.399G>T | p.Glu133Asp | p.E133D | protein_coding | deleterious(0.04) | benign(0.043) | TCGA-AJ-A5DW-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <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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