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Gene: NIPSNAP1 |
Gene summary for NIPSNAP1 |
| Gene information | Species | Human | Gene symbol | NIPSNAP1 | Gene ID | 8508 |
| Gene name | nipsnap homolog 1 | |
| Gene Alias | NIPSNAP1 | |
| Cytomap | 22q12.2 | |
| Gene Type | protein-coding | GO ID | GO:0003008 | UniProtAcc | B4DQI7 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 8508 | NIPSNAP1 | HCC1_Meng | Human | Liver | HCC | 1.76e-85 | 4.52e-01 | 0.0246 |
| 8508 | NIPSNAP1 | HCC2_Meng | Human | Liver | HCC | 1.84e-13 | 3.01e-02 | 0.0107 |
| 8508 | NIPSNAP1 | cirrhotic2 | Human | Liver | Cirrhotic | 1.55e-03 | 1.39e-01 | 0.0201 |
| 8508 | NIPSNAP1 | HCC1 | Human | Liver | HCC | 1.58e-14 | 4.64e+00 | 0.5336 |
| 8508 | NIPSNAP1 | HCC2 | Human | Liver | HCC | 1.12e-43 | 5.37e+00 | 0.5341 |
| 8508 | NIPSNAP1 | Pt13.b | Human | Liver | HCC | 8.68e-09 | 1.48e-01 | 0.0251 |
| 8508 | NIPSNAP1 | Pt14.a | Human | Liver | HCC | 1.86e-15 | 7.24e-01 | 0.0169 |
| 8508 | NIPSNAP1 | Pt14.b | Human | Liver | HCC | 1.31e-05 | 3.04e-01 | 0.018 |
| 8508 | NIPSNAP1 | S014 | Human | Liver | HCC | 7.93e-47 | 1.56e+00 | 0.2254 |
| 8508 | NIPSNAP1 | S015 | Human | Liver | HCC | 8.18e-43 | 2.08e+00 | 0.2375 |
| 8508 | NIPSNAP1 | S016 | Human | Liver | HCC | 1.05e-48 | 1.54e+00 | 0.2243 |
| 8508 | NIPSNAP1 | S027 | Human | Liver | HCC | 3.18e-14 | 1.48e+00 | 0.2446 |
| 8508 | NIPSNAP1 | S028 | Human | Liver | HCC | 5.32e-41 | 2.00e+00 | 0.2503 |
| 8508 | NIPSNAP1 | S029 | Human | Liver | HCC | 5.19e-42 | 2.13e+00 | 0.2581 |
| 8508 | NIPSNAP1 | C04 | Human | Oral cavity | OSCC | 2.16e-15 | 7.32e-01 | 0.2633 |
| 8508 | NIPSNAP1 | C21 | Human | Oral cavity | OSCC | 7.88e-47 | 1.29e+00 | 0.2678 |
| 8508 | NIPSNAP1 | C30 | Human | Oral cavity | OSCC | 3.60e-26 | 1.09e+00 | 0.3055 |
| 8508 | NIPSNAP1 | C38 | Human | Oral cavity | OSCC | 2.72e-12 | 1.18e+00 | 0.172 |
| 8508 | NIPSNAP1 | C43 | Human | Oral cavity | OSCC | 2.59e-42 | 7.01e-01 | 0.1704 |
| 8508 | NIPSNAP1 | C46 | Human | Oral cavity | OSCC | 4.63e-45 | 8.75e-01 | 0.1673 |
| Page: 1 2 3 4 5 6 |
| ∗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 |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
| 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 |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| Page: 1 |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| Page: 1 |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
| Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
| Page: 1 |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
| 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. |
| Page: 1 |
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Somatic mutation of malignant transformation related genes |
Annotation of somatic variants for genes involved in malignant transformation |
| 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 |
| NIPSNAP1 | SNV | Missense_Mutation | c.634N>G | p.Gln212Glu | p.Q212E | Q9BPW8 | protein_coding | deleterious(0) | benign(0.349) | TCGA-EK-A2PG-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
| NIPSNAP1 | SNV | Missense_Mutation | c.475N>A | p.Leu159Met | p.L159M | Q9BPW8 | protein_coding | deleterious(0) | probably_damaging(0.982) | TCGA-AA-3713-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Chemotherapy | 5-fluorouracil | PR | |
| NIPSNAP1 | SNV | Missense_Mutation | c.740N>A | p.Arg247Gln | p.R247Q | Q9BPW8 | protein_coding | deleterious(0.03) | possibly_damaging(0.629) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
| NIPSNAP1 | SNV | Missense_Mutation | novel | c.745N>A | p.Ala249Thr | p.A249T | Q9BPW8 | protein_coding | tolerated(0.05) | benign(0.055) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| NIPSNAP1 | SNV | Missense_Mutation | novel | c.656N>A | p.Gly219Asp | p.G219D | Q9BPW8 | protein_coding | deleterious(0) | probably_damaging(0.988) | TCGA-AX-A1CE-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unspecific | Paclitaxel | SD |
| NIPSNAP1 | SNV | Missense_Mutation | c.307N>A | p.Asp103Asn | p.D103N | Q9BPW8 | protein_coding | tolerated(0.27) | benign(0.065) | TCGA-B5-A0JY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | SD | |
| NIPSNAP1 | SNV | Missense_Mutation | novel | c.356N>G | p.Gln119Arg | p.Q119R | Q9BPW8 | protein_coding | deleterious(0) | probably_damaging(0.922) | TCGA-B5-A1MW-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
| NIPSNAP1 | SNV | Missense_Mutation | c.525N>T | p.Glu175Asp | p.E175D | Q9BPW8 | protein_coding | tolerated(0.15) | benign(0.012) | TCGA-55-8092-01 | Lung | lung adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
| NIPSNAP1 | SNV | Missense_Mutation | c.631N>T | p.Arg211Trp | p.R211W | Q9BPW8 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-39-5019-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
| NIPSNAP1 | SNV | Missense_Mutation | c.458N>T | p.Arg153Met | p.R153M | Q9BPW8 | protein_coding | deleterious(0.01) | benign(0.375) | TCGA-66-2773-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
| (DGIdb 4.0) |
| Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
| Page: 1 |