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Gene: SH3BP1 |
Gene summary for SH3BP1 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | SH3BP1 | Gene ID | 23616 |
| Gene name | SH3 domain binding protein 1 | |
| Gene Alias | ARHGAP43 | |
| Cytomap | 22q13.1 | |
| Gene Type | protein-coding | GO ID | GO:0001667 | UniProtAcc | Q9Y3L3 |
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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 |
| 23616 | SH3BP1 | HTA11_3410_2000001011 | Human | Colorectum | AD | 2.84e-04 | 1.21e-01 | 0.0155 |
| 23616 | SH3BP1 | HTA11_2487_2000001011 | Human | Colorectum | SER | 3.70e-09 | 2.48e-01 | -0.1808 |
| 23616 | SH3BP1 | HTA11_1938_2000001011 | Human | Colorectum | AD | 8.58e-13 | 3.80e-01 | -0.0811 |
| 23616 | SH3BP1 | HTA11_78_2000001011 | Human | Colorectum | AD | 1.84e-03 | 1.43e-01 | -0.1088 |
| 23616 | SH3BP1 | HTA11_347_2000001011 | Human | Colorectum | AD | 8.14e-12 | 2.38e-01 | -0.1954 |
| 23616 | SH3BP1 | HTA11_3361_2000001011 | Human | Colorectum | AD | 1.41e-08 | 2.76e-01 | -0.1207 |
| 23616 | SH3BP1 | HTA11_83_2000001011 | Human | Colorectum | SER | 1.79e-04 | 1.89e-01 | -0.1526 |
| 23616 | SH3BP1 | HTA11_696_2000001011 | Human | Colorectum | AD | 5.26e-16 | 3.63e-01 | -0.1464 |
| 23616 | SH3BP1 | HTA11_866_2000001011 | Human | Colorectum | AD | 1.85e-08 | 2.15e-01 | -0.1001 |
| 23616 | SH3BP1 | HTA11_1391_2000001011 | Human | Colorectum | AD | 6.55e-21 | 5.27e-01 | -0.059 |
| 23616 | SH3BP1 | HTA11_2992_2000001011 | Human | Colorectum | SER | 2.44e-09 | 3.99e-01 | -0.1706 |
| 23616 | SH3BP1 | HTA11_5212_2000001011 | Human | Colorectum | AD | 8.16e-07 | 3.20e-01 | -0.2061 |
| 23616 | SH3BP1 | HTA11_546_2000001011 | Human | Colorectum | AD | 2.42e-10 | 3.45e-01 | -0.0842 |
| 23616 | SH3BP1 | HTA11_866_3004761011 | Human | Colorectum | AD | 9.76e-05 | 1.64e-01 | 0.096 |
| 23616 | SH3BP1 | HTA11_8622_2000001021 | Human | Colorectum | SER | 3.19e-02 | 1.60e-01 | 0.0528 |
| 23616 | SH3BP1 | HTA11_10623_2000001011 | Human | Colorectum | AD | 9.21e-08 | 3.16e-01 | -0.0177 |
| 23616 | SH3BP1 | HTA11_6801_2000001011 | Human | Colorectum | SER | 1.64e-05 | 3.27e-01 | 0.0171 |
| 23616 | SH3BP1 | HTA11_10711_2000001011 | Human | Colorectum | AD | 1.28e-04 | 1.62e-01 | 0.0338 |
| 23616 | SH3BP1 | HTA11_7696_3000711011 | Human | Colorectum | AD | 2.85e-07 | 2.46e-01 | 0.0674 |
| 23616 | SH3BP1 | HTA11_7469_2000001011 | Human | Colorectum | AD | 2.39e-03 | 3.72e-01 | -0.0124 |
| Page: 1 2 3 4 5 6 |
| 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 | ||
| Esophagus |  | ESCC: Esophageal squamous cell carcinoma |
| HGIN: High-grade intraepithelial neoplasias | ||
| LGIN: Low-grade intraepithelial neoplasias | ||
| 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 |
| ∗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:00432446 | Esophagus | ESCC | regulation of protein-containing complex disassembly | 75/8552 | 121/18723 | 2.17e-04 | 1.36e-03 | 75 |
| GO:003432918 | Esophagus | ESCC | cell junction assembly | 227/8552 | 420/18723 | 3.06e-04 | 1.83e-03 | 227 |
| GO:00613394 | Esophagus | ESCC | establishment or maintenance of monopolar cell polarity | 20/8552 | 25/18723 | 4.81e-04 | 2.69e-03 | 20 |
| GO:00350893 | Esophagus | ESCC | establishment of apical/basal cell polarity | 18/8552 | 22/18723 | 5.69e-04 | 3.10e-03 | 18 |
| GO:0035020 | Esophagus | ESCC | regulation of Rac protein signal transduction | 17/8552 | 21/18723 | 1.03e-03 | 5.19e-03 | 17 |
| GO:000166720 | Esophagus | ESCC | ameboidal-type cell migration | 250/8552 | 475/18723 | 1.22e-03 | 5.97e-03 | 250 |
| GO:0045198 | Esophagus | ESCC | establishment of epithelial cell apical/basal polarity | 14/8552 | 17/18723 | 2.22e-03 | 9.78e-03 | 14 |
| GO:00465789 | Esophagus | ESCC | regulation of Ras protein signal transduction | 106/8552 | 189/18723 | 2.49e-03 | 1.08e-02 | 106 |
| GO:00436245 | Esophagus | ESCC | cellular protein complex disassembly | 78/8552 | 136/18723 | 4.00e-03 | 1.62e-02 | 78 |
| GO:00350888 | Esophagus | ESCC | establishment or maintenance of apical/basal cell polarity | 32/8552 | 49/18723 | 4.39e-03 | 1.73e-02 | 32 |
| GO:00612458 | Esophagus | ESCC | establishment or maintenance of bipolar cell polarity | 32/8552 | 49/18723 | 4.39e-03 | 1.73e-02 | 32 |
| GO:004308715 | Esophagus | ESCC | regulation of GTPase activity | 183/8552 | 348/18723 | 5.34e-03 | 2.00e-02 | 183 |
| GO:00451978 | Esophagus | ESCC | establishment or maintenance of epithelial cell apical/basal polarity | 29/8552 | 44/18723 | 5.41e-03 | 2.02e-02 | 29 |
| GO:001063120 | Esophagus | ESCC | epithelial cell migration | 187/8552 | 357/18723 | 6.05e-03 | 2.23e-02 | 187 |
| GO:009013220 | Esophagus | ESCC | epithelium migration | 188/8552 | 360/18723 | 6.96e-03 | 2.54e-02 | 188 |
| GO:009013020 | Esophagus | ESCC | tissue migration | 190/8552 | 365/18723 | 7.91e-03 | 2.82e-02 | 190 |
| GO:005105610 | Esophagus | ESCC | regulation of small GTPase mediated signal transduction | 157/8552 | 302/18723 | 1.55e-02 | 4.98e-02 | 157 |
| GO:002241119 | Oral cavity | OSCC | cellular component disassembly | 283/7305 | 443/18723 | 9.57e-27 | 3.37e-24 | 283 |
| GO:003298410 | Oral cavity | OSCC | protein-containing complex disassembly | 136/7305 | 224/18723 | 3.42e-11 | 1.13e-09 | 136 |
| GO:190290320 | Oral cavity | OSCC | regulation of supramolecular fiber organization | 211/7305 | 383/18723 | 9.45e-11 | 2.88e-09 | 211 |
| Page: 1 2 3 4 5 6 7 8 9 10 11 |
| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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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 |
| SH3BP1 | SNV | Missense_Mutation | c.147C>G | p.Ile49Met | p.I49M | Q9Y3L3 | protein_coding | deleterious(0.02) | possibly_damaging(0.541) | TCGA-AN-A0XP-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
| SH3BP1 | SNV | Missense_Mutation | c.532A>G | p.Ser178Gly | p.S178G | Q9Y3L3 | protein_coding | tolerated(0.33) | benign(0.015) | TCGA-D8-A1XK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicine+cyclophosphamide | SD | |
| SH3BP1 | SNV | Missense_Mutation | novel | c.1623A>C | p.Arg541Ser | p.R541S | Q9Y3L3 | protein_coding | deleterious(0.04) | benign(0.01) | TCGA-E2-A1L8-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD |
| SH3BP1 | insertion | In_Frame_Ins | novel | c.1105_1106insGTTCTGCTCCGACCCGCACGC | p.Met369delinsSerSerAlaProThrArgThrLeu | p.M369delinsSSAPTRTL | Q9Y3L3 | protein_coding | TCGA-A7-A0D9-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | SD | ||
| SH3BP1 | insertion | In_Frame_Ins | novel | c.705_706insTCGATGGGCAGG | p.Ala235_Asp236insSerMetGlyArg | p.A235_D236insSMGR | Q9Y3L3 | protein_coding | TCGA-A8-A093-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | ||
| SH3BP1 | insertion | Nonsense_Mutation | novel | c.630_631insAAGAATGACTGAATGGTGAATAACAGGTCACTGT | p.Ala211LysfsTer4 | p.A211Kfs*4 | Q9Y3L3 | protein_coding | TCGA-A8-A09W-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | ||
| SH3BP1 | SNV | Missense_Mutation | novel | c.552N>A | p.Met184Ile | p.M184I | Q9Y3L3 | protein_coding | tolerated(0.14) | benign(0.001) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| SH3BP1 | SNV | Missense_Mutation | rs754015130 | c.1372N>A | p.Val458Ile | p.V458I | Q9Y3L3 | protein_coding | tolerated(0.82) | benign(0.153) | TCGA-EA-A3HS-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
| SH3BP1 | SNV | Missense_Mutation | novel | c.307G>A | p.Ala103Thr | p.A103T | Q9Y3L3 | protein_coding | tolerated(0.46) | benign(0.253) | TCGA-EA-A410-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |
| SH3BP1 | SNV | Missense_Mutation | c.1537N>A | p.Pro513Thr | p.P513T | Q9Y3L3 | protein_coding | tolerated(0.18) | benign(0.031) | TCGA-IR-A3LA-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
| Page: 1 2 3 4 5 |
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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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