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Gene: SYNGR2 |
Gene summary for SYNGR2 |
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Gene information | Species | Human | Gene symbol | SYNGR2 | Gene ID | 9144 |
Gene name | synaptogyrin 2 | |
Gene Alias | SYNGR2 | |
Cytomap | 17q25.3 | |
Gene Type | protein-coding | GO ID | GO:0006810 | UniProtAcc | O43760 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
9144 | SYNGR2 | GSM4909281 | Human | Breast | IDC | 9.03e-05 | 2.50e-01 | 0.21 |
9144 | SYNGR2 | GSM4909282 | Human | Breast | IDC | 1.04e-08 | 3.45e-01 | -0.0288 |
9144 | SYNGR2 | GSM4909290 | Human | Breast | IDC | 4.66e-14 | 5.61e-01 | 0.2096 |
9144 | SYNGR2 | GSM4909291 | Human | Breast | IDC | 2.21e-13 | 5.49e-01 | 0.1753 |
9144 | SYNGR2 | GSM4909293 | Human | Breast | IDC | 3.06e-44 | 6.83e-01 | 0.1581 |
9144 | SYNGR2 | GSM4909296 | Human | Breast | IDC | 3.04e-06 | -5.70e-02 | 0.1524 |
9144 | SYNGR2 | GSM4909297 | Human | Breast | IDC | 1.97e-05 | -9.17e-02 | 0.1517 |
9144 | SYNGR2 | GSM4909298 | Human | Breast | IDC | 7.21e-09 | 2.90e-01 | 0.1551 |
9144 | SYNGR2 | GSM4909301 | Human | Breast | IDC | 7.72e-06 | 2.65e-01 | 0.1577 |
9144 | SYNGR2 | GSM4909305 | Human | Breast | IDC | 3.03e-02 | 3.12e-01 | 0.0436 |
9144 | SYNGR2 | GSM4909306 | Human | Breast | IDC | 6.40e-04 | 2.05e-01 | 0.1564 |
9144 | SYNGR2 | GSM4909311 | Human | Breast | IDC | 2.32e-24 | 2.93e-02 | 0.1534 |
9144 | SYNGR2 | GSM4909312 | Human | Breast | IDC | 1.96e-24 | 4.38e-01 | 0.1552 |
9144 | SYNGR2 | GSM4909317 | Human | Breast | IDC | 8.35e-12 | 4.97e-01 | 0.1355 |
9144 | SYNGR2 | GSM4909319 | Human | Breast | IDC | 8.33e-47 | 3.25e-01 | 0.1563 |
9144 | SYNGR2 | GSM4909320 | Human | Breast | IDC | 2.23e-12 | 4.72e-01 | 0.1575 |
9144 | SYNGR2 | GSM4909321 | Human | Breast | IDC | 1.71e-23 | 3.93e-01 | 0.1559 |
9144 | SYNGR2 | brca1 | Human | Breast | Precancer | 2.49e-04 | 2.38e-01 | -0.0338 |
9144 | SYNGR2 | brca2 | Human | Breast | Precancer | 8.75e-13 | 3.34e-01 | -0.024 |
9144 | SYNGR2 | brca3 | Human | Breast | Precancer | 1.17e-09 | 3.17e-01 | -0.0263 |
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∗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:0006887 | Colorectum | AD | exocytosis | 96/3918 | 352/18723 | 2.48e-03 | 1.90e-02 | 96 |
GO:00068871 | Colorectum | SER | exocytosis | 75/2897 | 352/18723 | 2.05e-03 | 2.03e-02 | 75 |
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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 |
SYNGR2 | SNV | Missense_Mutation | rs370411109 | c.659N>T | p.Pro220Leu | p.P220L | O43760 | protein_coding | tolerated(0.1) | probably_damaging(0.999) | TCGA-CD-8528-01 | Stomach | stomach adenocarcinoma | Female | <65 | III/IV | Chemotherapy | epirubicin | CR |
SYNGR2 | SNV | Missense_Mutation | c.577N>A | p.Ala193Thr | p.A193T | O43760 | protein_coding | tolerated(0.61) | benign(0) | TCGA-CD-A4MJ-01 | Stomach | stomach adenocarcinoma | Male | <65 | I/II | Chemotherapy | cisplatin | CR | |
SYNGR2 | SNV | Missense_Mutation | c.540T>A | p.Asn180Lys | p.N180K | O43760 | protein_coding | tolerated(0.35) | benign(0.037) | TCGA-D7-6528-01 | Stomach | stomach adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
SYNGR2 | SNV | Missense_Mutation | novel | c.626C>T | p.Thr209Ile | p.T209I | O43760 | protein_coding | deleterious(0.03) | possibly_damaging(0.723) | TCGA-D7-6820-01 | Stomach | stomach adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
SYNGR2 | SNV | Missense_Mutation | novel | c.124N>C | p.Cys42Arg | p.C42R | O43760 | protein_coding | deleterious(0) | probably_damaging(0.977) | TCGA-D7-A6EY-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
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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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