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Gene: GC |
Gene summary for GC |
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Gene information | Species | Human | Gene symbol | GC | Gene ID | 2638 |
Gene name | GC vitamin D binding protein | |
Gene Alias | DBP | |
Cytomap | 4q13.3 | |
Gene Type | protein-coding | GO ID | GO:0006629 | UniProtAcc | P02774 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
2638 | GC | S41 | Human | Liver | Cirrhotic | 1.46e-05 | -9.54e-01 | -0.0343 |
2638 | GC | S42 | Human | Liver | HCC | 7.42e-03 | -4.85e-01 | -0.0103 |
2638 | GC | S43 | Human | Liver | Cirrhotic | 6.46e-26 | -4.03e-01 | -0.0187 |
2638 | GC | S44 | Human | Liver | HCC | 2.81e-02 | -6.59e-01 | -0.0083 |
2638 | GC | HCC1_Meng | Human | Liver | HCC | 4.12e-31 | -1.56e-01 | 0.0246 |
2638 | GC | HCC2_Meng | Human | Liver | HCC | 2.71e-67 | -1.43e+00 | 0.0107 |
2638 | GC | cirrhotic2 | Human | Liver | Cirrhotic | 7.17e-07 | 2.86e-01 | 0.0201 |
2638 | GC | cirrhotic3 | Human | Liver | Cirrhotic | 1.28e-16 | -6.78e-01 | 0.0215 |
2638 | GC | p6 | Human | Liver | Cyst | 1.86e-19 | -1.48e+00 | -0.0218 |
2638 | GC | HCC1 | Human | Liver | HCC | 8.30e-06 | 3.63e+00 | 0.5336 |
2638 | GC | HCC2 | Human | Liver | HCC | 2.81e-27 | 6.74e+00 | 0.5341 |
2638 | GC | HCC5 | Human | Liver | HCC | 7.54e-16 | 3.23e+00 | 0.4932 |
2638 | GC | Pt13.a | Human | Liver | HCC | 2.71e-17 | -3.89e-01 | 0.021 |
2638 | GC | Pt13.b | Human | Liver | HCC | 6.04e-34 | -4.40e-01 | 0.0251 |
2638 | GC | Pt13.c | Human | Liver | HCC | 6.46e-04 | -5.40e-01 | 0.0076 |
2638 | GC | Pt14.a | Human | Liver | HCC | 2.30e-04 | -5.47e-01 | 0.0169 |
2638 | GC | Pt14.b | Human | Liver | HCC | 2.36e-08 | -3.18e-01 | 0.018 |
2638 | GC | Pt14.c | Human | Liver | HCC | 7.42e-04 | -7.82e-01 | 0.0054 |
2638 | GC | Pt14.d | Human | Liver | HCC | 1.58e-08 | -4.24e-01 | 0.0143 |
2638 | GC | S014 | Human | Liver | HCC | 2.61e-43 | -5.95e-01 | 0.2254 |
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Tissue | Expression Dynamics | Abbreviation |
Liver | ![]() | HCC: Hepatocellular carcinoma |
NAFLD: Non-alcoholic fatty liver disease |
∗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:1904035 | Liver | Cirrhotic | regulation of epithelial cell apoptotic process | 35/4634 | 96/18723 | 6.94e-03 | 3.38e-02 | 35 |
GO:0033197 | Liver | Cirrhotic | response to vitamin E | 7/4634 | 11/18723 | 7.11e-03 | 3.41e-02 | 7 |
GO:00459121 | Liver | Cirrhotic | negative regulation of carbohydrate metabolic process | 20/4634 | 48/18723 | 7.37e-03 | 3.52e-02 | 20 |
GO:19035794 | Liver | Cirrhotic | negative regulation of ATP metabolic process | 14/4634 | 30/18723 | 7.40e-03 | 3.53e-02 | 14 |
GO:00106771 | Liver | Cirrhotic | negative regulation of cellular carbohydrate metabolic process | 18/4634 | 42/18723 | 7.64e-03 | 3.61e-02 | 18 |
GO:00550901 | Liver | Cirrhotic | acylglycerol homeostasis | 18/4634 | 42/18723 | 7.64e-03 | 3.61e-02 | 18 |
GO:00703281 | Liver | Cirrhotic | triglyceride homeostasis | 18/4634 | 42/18723 | 7.64e-03 | 3.61e-02 | 18 |
GO:0045923 | Liver | Cirrhotic | positive regulation of fatty acid metabolic process | 17/4634 | 39/18723 | 7.71e-03 | 3.63e-02 | 17 |
GO:00512252 | Liver | Cirrhotic | spindle assembly | 41/4634 | 117/18723 | 8.08e-03 | 3.79e-02 | 41 |
GO:00454442 | Liver | Cirrhotic | fat cell differentiation | 73/4634 | 229/18723 | 8.57e-03 | 3.97e-02 | 73 |
GO:0071230 | Liver | Cirrhotic | cellular response to amino acid stimulus | 27/4634 | 71/18723 | 8.90e-03 | 4.11e-02 | 27 |
GO:00092065 | Liver | Cirrhotic | purine ribonucleoside triphosphate biosynthetic process | 26/4634 | 68/18723 | 9.37e-03 | 4.29e-02 | 26 |
GO:0009071 | Liver | Cirrhotic | serine family amino acid catabolic process | 8/4634 | 14/18723 | 9.65e-03 | 4.35e-02 | 8 |
GO:00454721 | Liver | Cirrhotic | response to ether | 8/4634 | 14/18723 | 9.65e-03 | 4.35e-02 | 8 |
GO:1901857 | Liver | Cirrhotic | positive regulation of cellular respiration | 8/4634 | 14/18723 | 9.65e-03 | 4.35e-02 | 8 |
GO:012025411 | Liver | Cirrhotic | olefinic compound metabolic process | 51/4634 | 153/18723 | 1.03e-02 | 4.61e-02 | 51 |
GO:0006497 | Liver | Cirrhotic | protein lipidation | 33/4634 | 92/18723 | 1.12e-02 | 4.92e-02 | 33 |
GO:002261322 | Liver | HCC | ribonucleoprotein complex biogenesis | 355/7958 | 463/18723 | 7.76e-52 | 4.92e-48 | 355 |
GO:001049822 | Liver | HCC | proteasomal protein catabolic process | 351/7958 | 490/18723 | 6.92e-40 | 1.46e-36 | 351 |
GO:000838022 | Liver | HCC | RNA splicing | 313/7958 | 434/18723 | 1.36e-36 | 1.73e-33 | 313 |
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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 |
GC | SNV | Missense_Mutation | c.1096A>G | p.Thr366Ala | p.T366A | P02774 | protein_coding | tolerated(0.35) | benign(0.093) | TCGA-A8-A09Z-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
GC | SNV | Missense_Mutation | novel | c.1236G>T | p.Lys412Asn | p.K412N | P02774 | protein_coding | tolerated(0.22) | benign(0.04) | TCGA-PE-A5DE-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | CR |
GC | insertion | Frame_Shift_Ins | novel | c.41_42insTA | p.Arg14SerfsTer8 | p.R14Sfs*8 | P02774 | protein_coding | TCGA-A2-A0EQ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | ||
GC | insertion | Nonsense_Mutation | novel | c.40_41insACATTTATTAAGCAGTATTCCATGGAATGGGGAATCAATTA | p.Arg14AsnfsTer4 | p.R14Nfs*4 | P02774 | protein_coding | TCGA-A2-A0EQ-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD | ||
GC | SNV | Missense_Mutation | c.1112G>A | p.Arg371Lys | p.R371K | P02774 | protein_coding | deleterious(0.02) | benign(0.333) | TCGA-AA-3982-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
GC | SNV | Missense_Mutation | c.858G>T | p.Glu286Asp | p.E286D | P02774 | protein_coding | tolerated(1) | benign(0.005) | TCGA-AA-3982-01 | Colorectum | colon adenocarcinoma | Male | >=65 | III/IV | Unknown | Unknown | SD | |
GC | SNV | Missense_Mutation | c.860N>T | p.Ser287Phe | p.S287F | P02774 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
GC | SNV | Missense_Mutation | c.818N>A | p.Leu273Gln | p.L273Q | P02774 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-AU-3779-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
GC | SNV | Missense_Mutation | c.356C>A | p.Ser119Tyr | p.S119Y | P02774 | protein_coding | deleterious(0) | probably_damaging(0.992) | TCGA-CA-6718-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | PD | |
GC | SNV | Missense_Mutation | rs746394990 | c.295G>C | p.Asp99His | p.D99H | P02774 | protein_coding | deleterious(0.02) | possibly_damaging(0.9) | TCGA-AG-A00Y-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | 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 |
2638 | GC | DRUGGABLE GENOME | inhibitor | CHEMBL712 | ANISINDIONE | |
2638 | GC | DRUGGABLE GENOME | cetuximab | CETUXIMAB | 29208668 | |
2638 | GC | DRUGGABLE GENOME | Isosorbide Dinitrate | |||
2638 | GC | DRUGGABLE GENOME | VITAMIN D | 761406 | ||
2638 | GC | DRUGGABLE GENOME | CHEMBL2105671 | AFEGOSTAT TARTRATE | ||
2638 | GC | DRUGGABLE GENOME | bevacizumab | BEVACIZUMAB | 29208668 | |
2638 | GC | DRUGGABLE GENOME | Pirsidomine | PIRSIDOMINE | ||
2638 | GC | DRUGGABLE GENOME | Erythrityl Tetranitrate | |||
2638 | GC | DRUGGABLE GENOME | ASA | ASPIRIN | 17555340 | |
2638 | GC | DRUGGABLE GENOME | Nitric Oxide |
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