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Gene: BNIP2 |
Gene summary for BNIP2 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | BNIP2 | Gene ID | 663 |
| Gene name | BCL2 interacting protein 2 | |
| Gene Alias | BNIP-2 | |
| Cytomap | 15q22.2 | |
| Gene Type | protein-coding | GO ID | GO:0006915 | UniProtAcc | Q12982 |
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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 |
| Malignant transformation involving gene list. |
| Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
| 663 | BNIP2 | LZE2T | Human | Esophagus | ESCC | 7.11e-04 | 4.59e-01 | 0.082 |
| 663 | BNIP2 | LZE4T | Human | Esophagus | ESCC | 7.15e-17 | 4.24e-01 | 0.0811 |
| 663 | BNIP2 | LZE5T | Human | Esophagus | ESCC | 4.48e-02 | 2.12e-01 | 0.0514 |
| 663 | BNIP2 | LZE7T | Human | Esophagus | ESCC | 2.56e-07 | 7.83e-01 | 0.0667 |
| 663 | BNIP2 | LZE8T | Human | Esophagus | ESCC | 1.02e-10 | 4.66e-01 | 0.067 |
| 663 | BNIP2 | LZE20T | Human | Esophagus | ESCC | 5.78e-04 | 4.35e-02 | 0.0662 |
| 663 | BNIP2 | LZE24T | Human | Esophagus | ESCC | 1.59e-12 | 3.09e-01 | 0.0596 |
| 663 | BNIP2 | LZE21T | Human | Esophagus | ESCC | 9.13e-03 | 3.79e-01 | 0.0655 |
| 663 | BNIP2 | LZE6T | Human | Esophagus | ESCC | 3.38e-05 | 3.25e-01 | 0.0845 |
| 663 | BNIP2 | P1T-E | Human | Esophagus | ESCC | 1.28e-12 | 8.47e-01 | 0.0875 |
| 663 | BNIP2 | P2T-E | Human | Esophagus | ESCC | 7.65e-32 | 6.44e-01 | 0.1177 |
| 663 | BNIP2 | P4T-E | Human | Esophagus | ESCC | 1.86e-32 | 8.98e-01 | 0.1323 |
| 663 | BNIP2 | P5T-E | Human | Esophagus | ESCC | 7.13e-28 | 3.96e-01 | 0.1327 |
| 663 | BNIP2 | P8T-E | Human | Esophagus | ESCC | 3.02e-35 | 7.02e-01 | 0.0889 |
| 663 | BNIP2 | P9T-E | Human | Esophagus | ESCC | 4.20e-18 | 4.56e-01 | 0.1131 |
| 663 | BNIP2 | P10T-E | Human | Esophagus | ESCC | 6.95e-35 | 6.58e-01 | 0.116 |
| 663 | BNIP2 | P11T-E | Human | Esophagus | ESCC | 5.97e-14 | 4.27e-01 | 0.1426 |
| 663 | BNIP2 | P12T-E | Human | Esophagus | ESCC | 7.48e-25 | 6.62e-01 | 0.1122 |
| 663 | BNIP2 | P15T-E | Human | Esophagus | ESCC | 3.31e-28 | 6.86e-01 | 0.1149 |
| 663 | BNIP2 | P16T-E | Human | Esophagus | ESCC | 3.88e-30 | 6.34e-01 | 0.1153 |
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| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| Liver |  | HCC: Hepatocellular carcinoma |
| NAFLD: Non-alcoholic fatty liver disease | ||
| Oral Cavity |  | EOLP: Erosive Oral lichen planus |
| LP: leukoplakia | ||
| NEOLP: Non-erosive oral lichen planus | ||
| OSCC: Oral squamous cell carcinoma | ||
| Skin |  | AK: Actinic keratosis |
| cSCC: Cutaneous squamous cell carcinoma | ||
| SCCIS:squamous cell carcinoma in situ | ||
| Thyroid |  | ATC: Anaplastic thyroid cancer |
| HT: Hashimoto's thyroiditis | ||
| PTC: Papillary thyroid cancer |
| ∗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 |
| Figure of enriched GO biological processes. |
| 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 |
| Enriched GO biological processes. |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:0070482113 | Thyroid | PTC | response to oxygen levels | 167/5968 | 347/18723 | 1.51e-10 | 5.03e-09 | 167 |
| GO:0036293113 | Thyroid | PTC | response to decreased oxygen levels | 153/5968 | 322/18723 | 2.71e-09 | 7.52e-08 | 153 |
| GO:0031667113 | Thyroid | PTC | response to nutrient levels | 201/5968 | 474/18723 | 7.00e-07 | 1.10e-05 | 201 |
| GO:007048228 | Thyroid | ATC | response to oxygen levels | 193/6293 | 347/18723 | 1.83e-17 | 1.93e-15 | 193 |
| GO:003629328 | Thyroid | ATC | response to decreased oxygen levels | 177/6293 | 322/18723 | 1.81e-15 | 1.32e-13 | 177 |
| GO:0031667210 | Thyroid | ATC | response to nutrient levels | 212/6293 | 474/18723 | 2.37e-07 | 3.70e-06 | 212 |
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| Enriched KEGG pathways. |
| 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 |
| BNIP2 | SNV | Missense_Mutation | c.1063G>A | p.Asp355Asn | p.D355N | protein_coding | deleterious(0.03) | possibly_damaging(0.686) | TCGA-C8-A26Y-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
| BNIP2 | SNV | Missense_Mutation | novel | c.1300G>C | p.Glu434Gln | p.E434Q | protein_coding | deleterious_low_confidence(0.01) | benign(0.086) | TCGA-OL-A5RW-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | CR | |
| BNIP2 | SNV | Missense_Mutation | c.736G>C | p.Glu246Gln | p.E246Q | protein_coding | tolerated(0.07) | possibly_damaging(0.84) | TCGA-EK-A2RJ-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD | ||
| BNIP2 | SNV | Missense_Mutation | novel | c.860N>T | p.Ala287Val | p.A287V | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-A6-3809-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| BNIP2 | SNV | Missense_Mutation | c.662N>G | p.Asp221Gly | p.D221G | protein_coding | deleterious(0.01) | probably_damaging(0.999) | TCGA-AA-3811-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | ||
| BNIP2 | SNV | Missense_Mutation | rs762238174 | c.449N>C | p.Ile150Thr | p.I150T | protein_coding | tolerated(0.46) | benign(0.007) | TCGA-AZ-4315-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
| BNIP2 | SNV | Missense_Mutation | c.1182A>T | p.Arg394Ser | p.R394S | protein_coding | deleterious(0.03) | possibly_damaging(0.786) | TCGA-D5-6537-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | PD | ||
| BNIP2 | SNV | Missense_Mutation | rs375444414 | c.1186N>A | p.Val396Met | p.V396M | protein_coding | deleterious(0.02) | probably_damaging(0.98) | TCGA-AJ-A3BH-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | Unknown | I/II | Unknown | Unknown | SD | |
| BNIP2 | SNV | Missense_Mutation | novel | c.410C>T | p.Pro137Leu | p.P137L | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-AJ-A5DW-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
| BNIP2 | SNV | Missense_Mutation | c.541C>A | p.Leu181Met | p.L181M | protein_coding | deleterious(0.01) | possibly_damaging(0.73) | TCGA-AP-A051-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=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 |
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