|
|||||
|
 | |
| |
| |
| |
| |
| |
|
Gene: PLXNB1 |
Gene summary for PLXNB1 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | PLXNB1 | Gene ID | 5364 |
| Gene name | plexin B1 | |
| Gene Alias | PLEXIN-B1 | |
| Cytomap | 3p21.31 | |
| Gene Type | protein-coding | GO ID | GO:0000902 | UniProtAcc | O43157 |
Top |
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 |
| 5364 | PLXNB1 | HTA11_3410_2000001011 | Human | Colorectum | AD | 2.96e-06 | 1.55e-01 | 0.0155 |
| 5364 | PLXNB1 | HTA11_866_3004761011 | Human | Colorectum | AD | 3.53e-03 | 2.37e-01 | 0.096 |
| 5364 | PLXNB1 | HTA11_7696_3000711011 | Human | Colorectum | AD | 3.19e-04 | 1.87e-01 | 0.0674 |
| 5364 | PLXNB1 | HTA11_99999971662_82457 | Human | Colorectum | MSS | 8.10e-11 | 5.97e-01 | 0.3859 |
| 5364 | PLXNB1 | HTA11_99999974143_84620 | Human | Colorectum | MSS | 2.98e-04 | 3.70e-01 | 0.3005 |
| 5364 | PLXNB1 | A015-C-203 | Human | Colorectum | FAP | 3.18e-08 | 3.81e-01 | -0.1294 |
| 5364 | PLXNB1 | A002-C-201 | Human | Colorectum | FAP | 3.61e-02 | 4.33e-01 | 0.0324 |
| 5364 | PLXNB1 | A015-C-104 | Human | Colorectum | FAP | 1.06e-03 | 2.48e-01 | -0.1899 |
| 5364 | PLXNB1 | CRC-3-11773 | Human | Colorectum | CRC | 5.74e-06 | 5.15e-01 | 0.2564 |
| 5364 | PLXNB1 | AEH-subject1 | Human | Endometrium | AEH | 1.09e-09 | 4.53e-01 | -0.3059 |
| 5364 | PLXNB1 | AEH-subject2 | Human | Endometrium | AEH | 9.54e-11 | 4.57e-01 | -0.2525 |
| 5364 | PLXNB1 | AEH-subject3 | Human | Endometrium | AEH | 7.88e-05 | 2.57e-01 | -0.2576 |
| 5364 | PLXNB1 | EEC-subject2 | Human | Endometrium | EEC | 1.88e-16 | 5.80e-01 | -0.2607 |
| 5364 | PLXNB1 | GSM6177620_NYU_UCEC1_lib1_lib1 | Human | Endometrium | EEC | 1.95e-04 | 4.50e-02 | -0.1869 |
| 5364 | PLXNB1 | GSM6177620_NYU_UCEC1_lib2_lib2 | Human | Endometrium | EEC | 1.29e-06 | 1.12e-01 | -0.1875 |
| 5364 | PLXNB1 | GSM6177620_NYU_UCEC1_lib3_lib3 | Human | Endometrium | EEC | 5.56e-07 | 3.45e-02 | -0.1883 |
| 5364 | PLXNB1 | GSM6177621_NYU_UCEC2_lib1_lib1 | Human | Endometrium | EEC | 1.35e-06 | 3.03e-01 | -0.1934 |
| 5364 | PLXNB1 | GSM6177622_NYU_UCEC3_lib1_lib1 | Human | Endometrium | EEC | 5.18e-08 | 1.00e-01 | -0.1917 |
| 5364 | PLXNB1 | GSM6177622_NYU_UCEC3_lib2_lib2 | Human | Endometrium | EEC | 1.55e-06 | 1.08e-01 | -0.1916 |
| 5364 | PLXNB1 | GSM6177623_NYU_UCEC3_Vis | Human | Endometrium | EEC | 1.12e-51 | 1.07e+00 | -0.1269 |
| Page: 1 2 3 4 5 6 7 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Colorectum (GSE201348) |  | FAP: Familial adenomatous polyposis |
| CRC: Colorectal cancer | ||
| Colorectum (HTA11) |  | AD: Adenomas |
| SER: Sessile serrated lesions | ||
| MSI-H: Microsatellite-high colorectal cancer | ||
| MSS: Microsatellite stable colorectal cancer | ||
| Endometrium |  | AEH: Atypical endometrial hyperplasia |
| EEC: Endometrioid Cancer | ||
| 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 | ||
| Prostate |  | BPH: Benign Prostatic Hyperplasia |
| 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. |
Top |
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:00519606 | Esophagus | ESCC | regulation of nervous system development | 237/8552 | 443/18723 | 5.02e-04 | 2.78e-03 | 237 |
| GO:00519625 | Esophagus | ESCC | positive regulation of nervous system development | 149/8552 | 272/18723 | 1.50e-03 | 7.06e-03 | 149 |
| GO:00603485 | Esophagus | ESCC | bone development | 115/8552 | 205/18723 | 1.67e-03 | 7.72e-03 | 115 |
| GO:000740915 | Esophagus | ESCC | axonogenesis | 219/8552 | 418/18723 | 3.14e-03 | 1.31e-02 | 219 |
| GO:00507728 | Esophagus | ESCC | positive regulation of axonogenesis | 48/8552 | 79/18723 | 4.93e-03 | 1.89e-02 | 48 |
| GO:004308715 | Esophagus | ESCC | regulation of GTPase activity | 183/8552 | 348/18723 | 5.34e-03 | 2.00e-02 | 183 |
| GO:002260412 | Liver | Cirrhotic | regulation of cell morphogenesis | 127/4634 | 309/18723 | 1.45e-10 | 7.44e-09 | 127 |
| GO:000836012 | Liver | Cirrhotic | regulation of cell shape | 69/4634 | 154/18723 | 4.21e-08 | 1.36e-06 | 69 |
| GO:00107205 | Liver | Cirrhotic | positive regulation of cell development | 99/4634 | 298/18723 | 5.71e-04 | 4.46e-03 | 99 |
| GO:00015035 | Liver | Cirrhotic | ossification | 127/4634 | 408/18723 | 1.89e-03 | 1.19e-02 | 127 |
| GO:00071624 | Liver | Cirrhotic | negative regulation of cell adhesion | 93/4634 | 303/18723 | 1.06e-02 | 4.66e-02 | 93 |
| GO:002260422 | Liver | HCC | regulation of cell morphogenesis | 188/7958 | 309/18723 | 4.84e-11 | 1.82e-09 | 188 |
| GO:003134611 | Liver | HCC | positive regulation of cell projection organization | 193/7958 | 353/18723 | 2.28e-06 | 3.08e-05 | 193 |
| GO:000836022 | Liver | HCC | regulation of cell shape | 92/7958 | 154/18723 | 1.15e-05 | 1.31e-04 | 92 |
| GO:001072011 | Liver | HCC | positive regulation of cell development | 155/7958 | 298/18723 | 5.39e-04 | 3.48e-03 | 155 |
| GO:001097511 | Liver | HCC | regulation of neuron projection development | 220/7958 | 445/18723 | 1.68e-03 | 8.78e-03 | 220 |
| GO:00507674 | Liver | HCC | regulation of neurogenesis | 181/7958 | 364/18723 | 3.00e-03 | 1.40e-02 | 181 |
| GO:00507693 | Liver | HCC | positive regulation of neurogenesis | 116/7958 | 225/18723 | 3.67e-03 | 1.63e-02 | 116 |
| GO:00107209 | Oral cavity | OSCC | positive regulation of cell development | 159/7305 | 298/18723 | 3.06e-07 | 4.66e-06 | 159 |
| GO:002260419 | Oral cavity | OSCC | regulation of cell morphogenesis | 163/7305 | 309/18723 | 5.66e-07 | 8.19e-06 | 163 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa04360 | Colorectum | AD | Axon guidance | 61/2092 | 182/8465 | 4.36e-03 | 2.17e-02 | 1.38e-02 | 61 |
| hsa043601 | Colorectum | AD | Axon guidance | 61/2092 | 182/8465 | 4.36e-03 | 2.17e-02 | 1.38e-02 | 61 |
| hsa043602 | Colorectum | MSS | Axon guidance | 54/1875 | 182/8465 | 1.03e-02 | 3.69e-02 | 2.26e-02 | 54 |
| hsa043603 | Colorectum | MSS | Axon guidance | 54/1875 | 182/8465 | 1.03e-02 | 3.69e-02 | 2.26e-02 | 54 |
| hsa043604 | Colorectum | FAP | Axon guidance | 47/1404 | 182/8465 | 9.09e-04 | 5.20e-03 | 3.16e-03 | 47 |
| hsa043605 | Colorectum | FAP | Axon guidance | 47/1404 | 182/8465 | 9.09e-04 | 5.20e-03 | 3.16e-03 | 47 |
| hsa043606 | Colorectum | CRC | Axon guidance | 43/1091 | 182/8465 | 4.38e-05 | 8.70e-04 | 5.90e-04 | 43 |
| hsa043607 | Colorectum | CRC | Axon guidance | 43/1091 | 182/8465 | 4.38e-05 | 8.70e-04 | 5.90e-04 | 43 |
| hsa0436010 | Endometrium | AEH | Axon guidance | 39/1197 | 182/8465 | 4.47e-03 | 2.46e-02 | 1.80e-02 | 39 |
| hsa0436013 | Endometrium | AEH | Axon guidance | 39/1197 | 182/8465 | 4.47e-03 | 2.46e-02 | 1.80e-02 | 39 |
| hsa0436022 | Endometrium | EEC | Axon guidance | 39/1237 | 182/8465 | 7.78e-03 | 3.66e-02 | 2.73e-02 | 39 |
| hsa0436032 | Endometrium | EEC | Axon guidance | 39/1237 | 182/8465 | 7.78e-03 | 3.66e-02 | 2.73e-02 | 39 |
| hsa0436016 | Esophagus | ESCC | Axon guidance | 108/4205 | 182/8465 | 5.13e-03 | 1.30e-02 | 6.67e-03 | 108 |
| hsa0436017 | Esophagus | ESCC | Axon guidance | 108/4205 | 182/8465 | 5.13e-03 | 1.30e-02 | 6.67e-03 | 108 |
| hsa0436014 | Oral cavity | OSCC | Axon guidance | 97/3704 | 182/8465 | 5.59e-03 | 1.33e-02 | 6.76e-03 | 97 |
| hsa0436015 | Oral cavity | OSCC | Axon guidance | 97/3704 | 182/8465 | 5.59e-03 | 1.33e-02 | 6.76e-03 | 97 |
| Page: 1 |
Top |
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 |
| SEMA4A | PLXNB1 | SEMA4A_PLXNB1 | SEMA4 | Cervix | ADJ |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | Cervix | ADJ |
| SEMA4A | PLXNB1 | SEMA4A_PLXNB1 | SEMA4 | Cervix | CC |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | Cervix | CC |
| SEMA4A | PLXNB1 | SEMA4A_PLXNB1 | SEMA4 | CRC | AD |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | CRC | AD |
| SEMA4A | PLXNB1 | SEMA4A_PLXNB1 | SEMA4 | CRC | MSI-H |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | CRC | MSI-H |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | CRC | MSS |
| SEMA4A | PLXNB1 | SEMA4A_PLXNB1 | SEMA4 | CRC | SER |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | CRC | SER |
| SEMA4A | PLXNB1 | SEMA4A_PLXNB1 | SEMA4 | Endometrium | AEH |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | Endometrium | AEH |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | Endometrium | EEC |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | Endometrium | Healthy |
| SEMA4A | PLXNB1 | SEMA4A_PLXNB1 | SEMA4 | HNSCC | ADJ |
| SEMA4A | PLXNB1 | SEMA4A_PLXNB1 | SEMA4 | HNSCC | Precancer |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | HNSCC | Precancer |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | Liver | Healthy |
| SEMA4D | PLXNB1 | SEMA4D_PLXNB1 | SEMA4 | Liver | Precancer |
| Page: 1 |
Top |
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 |
Top |
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 |
| PLXNB1 | SNV | Missense_Mutation | c.6394G>T | p.Val2132Phe | p.V2132F | O43157 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-A2-A04Y-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | SD | |
| PLXNB1 | SNV | Missense_Mutation | novel | c.4634N>T | p.Thr1545Ile | p.T1545I | O43157 | protein_coding | deleterious(0) | probably_damaging(0.986) | TCGA-AC-A3W5-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | docetaxel | CR |
| PLXNB1 | SNV | Missense_Mutation | rs759375530 | c.1529N>A | p.Arg510His | p.R510H | O43157 | protein_coding | tolerated(0.09) | benign(0.015) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| PLXNB1 | SNV | Missense_Mutation | c.3088N>G | p.Ser1030Gly | p.S1030G | O43157 | protein_coding | deleterious(0) | probably_damaging(0.91) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
| PLXNB1 | SNV | Missense_Mutation | c.3085T>A | p.Cys1029Ser | p.C1029S | O43157 | protein_coding | deleterious(0) | possibly_damaging(0.82) | TCGA-AR-A24Z-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD | |
| PLXNB1 | SNV | Missense_Mutation | rs866132965 | c.2776N>T | p.Pro926Ser | p.P926S | O43157 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-D8-A1J8-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | nolvadex | SD |
| PLXNB1 | SNV | Missense_Mutation | c.5135N>A | p.Arg1712Gln | p.R1712Q | O43157 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-D8-A1JA-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | adriamycin | PD | |
| PLXNB1 | insertion | In_Frame_Ins | novel | c.1721_1722insTGGCCCGGGGTC | p.Glu574delinsAspGlyProGlySer | p.E574delinsDGPGS | O43157 | protein_coding | TCGA-B6-A0IK-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD | ||
| PLXNB1 | insertion | Frame_Shift_Ins | novel | c.1720_1721insGTCCCAGTGTGAGAGTTTTTCTC | p.Glu574GlyfsTer16 | p.E574Gfs*16 | O43157 | protein_coding | TCGA-B6-A0IK-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Unknown | Unknown | PD | ||
| PLXNB1 | deletion | Frame_Shift_Del | novel | c.4078delN | p.Leu1360TrpfsTer8 | p.L1360Wfs*8 | O43157 | protein_coding | TCGA-EW-A2FV-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | docetaxel | SD |
| Page: 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 |
Top |
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 |
Copyright 2023-Present -The University of Texas Health Science Center at Houston |