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Gene: NWD1 |
Gene summary for NWD1 |
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Gene information | Species | Human | Gene symbol | NWD1 | Gene ID | 284434 |
Gene name | NACHT and WD repeat domain containing 1 | |
Gene Alias | NWD1 | |
Cytomap | 19p13.11 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q149M9 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
284434 | NWD1 | HCC1 | Human | Liver | HCC | 7.03e-21 | 2.11e+00 | 0.5336 |
284434 | NWD1 | HCC2 | Human | Liver | HCC | 2.75e-38 | 2.24e+00 | 0.5341 |
284434 | NWD1 | HCC5 | Human | Liver | HCC | 4.48e-36 | 2.11e+00 | 0.4932 |
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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:00510902 | Liver | HCC | regulation of DNA-binding transcription factor activity | 220/7958 | 440/18723 | 8.04e-04 | 4.82e-03 | 220 |
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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 |
NWD1 | SNV | Missense_Mutation | rs141165642 | c.3964G>A | p.Val1322Ile | p.V1322I | Q149M9 | protein_coding | tolerated(0.22) | benign(0.043) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
NWD1 | SNV | Missense_Mutation | rs371438099 | c.2582N>A | p.Arg861Gln | p.R861Q | Q149M9 | protein_coding | tolerated(1) | benign(0.003) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
NWD1 | SNV | Missense_Mutation | rs372464599 | c.610N>A | p.Ala204Thr | p.A204T | Q149M9 | protein_coding | tolerated(0.32) | possibly_damaging(0.454) | TCGA-B5-A0JY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | SD |
NWD1 | SNV | Missense_Mutation | novel | c.1085N>G | p.Leu362Arg | p.L362R | Q149M9 | protein_coding | deleterious(0) | probably_damaging(0.976) | TCGA-B5-A11H-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Hormone Therapy | megace | SD |
NWD1 | SNV | Missense_Mutation | rs369799191 | c.2363N>A | p.Arg788His | p.R788H | Q149M9 | protein_coding | deleterious(0) | possibly_damaging(0.855) | TCGA-B5-A11H-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Hormone Therapy | megace | SD |
NWD1 | SNV | Missense_Mutation | novel | c.2327N>T | p.Ala776Val | p.A776V | Q149M9 | protein_coding | tolerated(0.23) | benign(0.027) | TCGA-B5-A1MR-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
NWD1 | SNV | Missense_Mutation | novel | c.2126A>G | p.Asp709Gly | p.D709G | Q149M9 | protein_coding | deleterious(0) | possibly_damaging(0.71) | TCGA-B5-A3FA-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NWD1 | SNV | Missense_Mutation | rs148020552 | c.3800G>A | p.Arg1267His | p.R1267H | Q149M9 | protein_coding | tolerated(0.21) | benign(0) | TCGA-B5-A3FA-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NWD1 | SNV | Missense_Mutation | rs148848880 | c.943C>T | p.Arg315Cys | p.R315C | Q149M9 | protein_coding | deleterious(0) | possibly_damaging(0.88) | TCGA-B5-A3FC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
NWD1 | SNV | Missense_Mutation | c.1405N>C | p.Cys469Arg | p.C469R | Q149M9 | protein_coding | tolerated(0.09) | probably_damaging(0.961) | TCGA-BG-A222-01 | 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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