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Gene: CDC23 |
Gene summary for CDC23 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | CDC23 | Gene ID | 8697 |
| Gene name | cell division cycle 23 | |
| Gene Alias | ANAPC8 | |
| Cytomap | 5q31.2 | |
| Gene Type | protein-coding | GO ID | GO:0000070 | UniProtAcc | Q9UJX2 |
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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 |
| 8697 | CDC23 | LZE4T | Human | Esophagus | ESCC | 1.12e-08 | 1.95e-01 | 0.0811 |
| 8697 | CDC23 | LZE8T | Human | Esophagus | ESCC | 3.86e-03 | 1.09e-01 | 0.067 |
| 8697 | CDC23 | LZE24T | Human | Esophagus | ESCC | 3.39e-13 | 2.38e-01 | 0.0596 |
| 8697 | CDC23 | P2T-E | Human | Esophagus | ESCC | 2.76e-21 | 3.87e-01 | 0.1177 |
| 8697 | CDC23 | P4T-E | Human | Esophagus | ESCC | 3.67e-16 | 3.57e-01 | 0.1323 |
| 8697 | CDC23 | P5T-E | Human | Esophagus | ESCC | 4.80e-27 | 4.68e-01 | 0.1327 |
| 8697 | CDC23 | P8T-E | Human | Esophagus | ESCC | 8.03e-10 | 1.58e-01 | 0.0889 |
| 8697 | CDC23 | P9T-E | Human | Esophagus | ESCC | 2.49e-12 | 1.94e-01 | 0.1131 |
| 8697 | CDC23 | P10T-E | Human | Esophagus | ESCC | 3.19e-21 | 2.87e-01 | 0.116 |
| 8697 | CDC23 | P11T-E | Human | Esophagus | ESCC | 5.30e-10 | 4.06e-01 | 0.1426 |
| 8697 | CDC23 | P12T-E | Human | Esophagus | ESCC | 2.38e-24 | 5.17e-01 | 0.1122 |
| 8697 | CDC23 | P15T-E | Human | Esophagus | ESCC | 4.63e-19 | 4.06e-01 | 0.1149 |
| 8697 | CDC23 | P16T-E | Human | Esophagus | ESCC | 4.29e-16 | 3.11e-01 | 0.1153 |
| 8697 | CDC23 | P17T-E | Human | Esophagus | ESCC | 9.24e-09 | 2.82e-01 | 0.1278 |
| 8697 | CDC23 | P19T-E | Human | Esophagus | ESCC | 5.86e-03 | 3.29e-01 | 0.1662 |
| 8697 | CDC23 | P20T-E | Human | Esophagus | ESCC | 4.52e-24 | 4.71e-01 | 0.1124 |
| 8697 | CDC23 | P21T-E | Human | Esophagus | ESCC | 4.93e-19 | 3.68e-01 | 0.1617 |
| 8697 | CDC23 | P22T-E | Human | Esophagus | ESCC | 6.45e-20 | 2.06e-01 | 0.1236 |
| 8697 | CDC23 | P23T-E | Human | Esophagus | ESCC | 1.53e-05 | 1.39e-01 | 0.108 |
| 8697 | CDC23 | P24T-E | Human | Esophagus | ESCC | 2.27e-15 | 1.73e-01 | 0.1287 |
| Page: 1 2 3 4 5 |
| 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 | ||
| 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:00070595 | Thyroid | PTC | chromosome segregation | 146/5968 | 346/18723 | 2.99e-05 | 2.87e-04 | 146 |
| GO:00008196 | Thyroid | PTC | sister chromatid segregation | 92/5968 | 202/18723 | 3.07e-05 | 2.94e-04 | 92 |
| GO:009006816 | Thyroid | PTC | positive regulation of cell cycle process | 103/5968 | 236/18723 | 9.03e-05 | 7.50e-04 | 103 |
| GO:00709796 | Thyroid | PTC | protein K11-linked ubiquitination | 19/5968 | 29/18723 | 2.02e-04 | 1.51e-03 | 19 |
| GO:00482855 | Thyroid | PTC | organelle fission | 188/5968 | 488/18723 | 9.64e-04 | 5.77e-03 | 188 |
| GO:00070805 | Thyroid | PTC | mitotic metaphase plate congression | 27/5968 | 50/18723 | 9.69e-04 | 5.79e-03 | 27 |
| GO:00070885 | Thyroid | PTC | regulation of mitotic nuclear division | 51/5968 | 110/18723 | 1.02e-03 | 6.07e-03 | 51 |
| GO:00988135 | Thyroid | PTC | nuclear chromosome segregation | 114/5968 | 281/18723 | 1.21e-03 | 6.94e-03 | 114 |
| GO:19019927 | Thyroid | PTC | positive regulation of mitotic cell cycle phase transition | 44/5968 | 93/18723 | 1.32e-03 | 7.48e-03 | 44 |
| GO:00519835 | Thyroid | PTC | regulation of chromosome segregation | 43/5968 | 91/18723 | 1.53e-03 | 8.55e-03 | 43 |
| GO:19019898 | Thyroid | PTC | positive regulation of cell cycle phase transition | 52/5968 | 115/18723 | 1.82e-03 | 9.84e-03 | 52 |
| GO:00500005 | Thyroid | PTC | chromosome localization | 39/5968 | 82/18723 | 2.14e-03 | 1.14e-02 | 39 |
| GO:19058184 | Thyroid | PTC | regulation of chromosome separation | 35/5968 | 72/18723 | 2.23e-03 | 1.18e-02 | 35 |
| GO:00513035 | Thyroid | PTC | establishment of chromosome localization | 38/5968 | 80/18723 | 2.49e-03 | 1.29e-02 | 38 |
| GO:00300714 | Thyroid | PTC | regulation of mitotic metaphase/anaphase transition | 30/5968 | 60/18723 | 2.60e-03 | 1.33e-02 | 30 |
| GO:00513105 | Thyroid | PTC | metaphase plate congression | 32/5968 | 65/18723 | 2.62e-03 | 1.34e-02 | 32 |
| GO:00002804 | Thyroid | PTC | nuclear division | 167/5968 | 439/18723 | 3.27e-03 | 1.60e-02 | 167 |
| GO:00513064 | Thyroid | PTC | mitotic sister chromatid separation | 32/5968 | 67/18723 | 4.75e-03 | 2.22e-02 | 32 |
| GO:00070914 | Thyroid | PTC | metaphase/anaphase transition of mitotic cell cycle | 30/5968 | 62/18723 | 4.85e-03 | 2.27e-02 | 30 |
| GO:00517833 | Thyroid | PTC | regulation of nuclear division | 59/5968 | 139/18723 | 5.50e-03 | 2.50e-02 | 59 |
| 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 |
| hsa0412027 | Esophagus | ESCC | Ubiquitin mediated proteolysis | 122/4205 | 142/8465 | 6.53e-20 | 7.29e-18 | 3.74e-18 | 122 |
| hsa0411023 | Esophagus | ESCC | Cell cycle | 126/4205 | 157/8465 | 1.34e-15 | 5.60e-14 | 2.87e-14 | 126 |
| hsa05166211 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
| hsa041146 | Esophagus | ESCC | Oocyte meiosis | 77/4205 | 131/8465 | 2.19e-02 | 4.80e-02 | 2.46e-02 | 77 |
| hsa0412036 | Esophagus | ESCC | Ubiquitin mediated proteolysis | 122/4205 | 142/8465 | 6.53e-20 | 7.29e-18 | 3.74e-18 | 122 |
| hsa0411033 | Esophagus | ESCC | Cell cycle | 126/4205 | 157/8465 | 1.34e-15 | 5.60e-14 | 2.87e-14 | 126 |
| hsa05166310 | Esophagus | ESCC | Human T-cell leukemia virus 1 infection | 164/4205 | 222/8465 | 8.13e-14 | 2.09e-12 | 1.07e-12 | 164 |
| hsa0411411 | Esophagus | ESCC | Oocyte meiosis | 77/4205 | 131/8465 | 2.19e-02 | 4.80e-02 | 2.46e-02 | 77 |
| hsa0412041 | Liver | HCC | Ubiquitin mediated proteolysis | 110/4020 | 142/8465 | 1.67e-13 | 3.74e-12 | 2.08e-12 | 110 |
| hsa041102 | Liver | HCC | Cell cycle | 106/4020 | 157/8465 | 2.54e-07 | 3.04e-06 | 1.69e-06 | 106 |
| hsa0516622 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
| hsa0412051 | Liver | HCC | Ubiquitin mediated proteolysis | 110/4020 | 142/8465 | 1.67e-13 | 3.74e-12 | 2.08e-12 | 110 |
| hsa041103 | Liver | HCC | Cell cycle | 106/4020 | 157/8465 | 2.54e-07 | 3.04e-06 | 1.69e-06 | 106 |
| hsa0516632 | Liver | HCC | Human T-cell leukemia virus 1 infection | 139/4020 | 222/8465 | 3.17e-06 | 2.79e-05 | 1.55e-05 | 139 |
| hsa041108 | Oral cavity | OSCC | Cell cycle | 118/3704 | 157/8465 | 7.15e-16 | 2.66e-14 | 1.35e-14 | 118 |
| hsa0412020 | Oral cavity | OSCC | Ubiquitin mediated proteolysis | 105/3704 | 142/8465 | 1.83e-13 | 4.37e-12 | 2.23e-12 | 105 |
| hsa0516630 | Oral cavity | OSCC | Human T-cell leukemia virus 1 infection | 150/3704 | 222/8465 | 3.68e-13 | 7.26e-12 | 3.70e-12 | 150 |
| hsa04114 | Oral cavity | OSCC | Oocyte meiosis | 74/3704 | 131/8465 | 2.13e-03 | 5.75e-03 | 2.92e-03 | 74 |
| hsa0411015 | Oral cavity | OSCC | Cell cycle | 118/3704 | 157/8465 | 7.15e-16 | 2.66e-14 | 1.35e-14 | 118 |
| hsa04120110 | Oral cavity | OSCC | Ubiquitin mediated proteolysis | 105/3704 | 142/8465 | 1.83e-13 | 4.37e-12 | 2.23e-12 | 105 |
| Page: 1 2 |
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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 |
| CDC23 | SNV | Missense_Mutation | novel | c.767N>T | p.Asp256Val | p.D256V | Q9UJX2 | protein_coding | tolerated(0.09) | benign(0.041) | TCGA-AC-A6IW-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| CDC23 | insertion | Frame_Shift_Ins | novel | c.419_420insACACCATA | p.Leu141HisfsTer9 | p.L141Hfs*9 | Q9UJX2 | protein_coding | TCGA-DS-A1OC-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | gemcitabine | SD | ||
| CDC23 | SNV | Missense_Mutation | rs767536014 | c.1031N>A | p.Arg344His | p.R344H | Q9UJX2 | protein_coding | deleterious(0.03) | possibly_damaging(0.862) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
| CDC23 | SNV | Missense_Mutation | c.938N>C | p.Lys313Thr | p.K313T | Q9UJX2 | protein_coding | deleterious(0.04) | benign(0.184) | TCGA-AA-3510-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| CDC23 | SNV | Missense_Mutation | novel | c.1747N>A | p.Pro583Thr | p.P583T | Q9UJX2 | protein_coding | tolerated(0.06) | benign(0.011) | TCGA-AA-3811-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
| CDC23 | SNV | Missense_Mutation | rs761053901 | c.1384G>A | p.Val462Met | p.V462M | Q9UJX2 | protein_coding | deleterious(0) | possibly_damaging(0.768) | TCGA-AA-3815-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
| CDC23 | SNV | Missense_Mutation | novel | c.1336N>G | p.Leu446Val | p.L446V | Q9UJX2 | protein_coding | deleterious(0.04) | possibly_damaging(0.842) | TCGA-AA-3979-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
| CDC23 | SNV | Missense_Mutation | c.1239N>T | p.Lys413Asn | p.K413N | Q9UJX2 | protein_coding | tolerated(0.07) | benign(0.14) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD | |
| CDC23 | SNV | Missense_Mutation | novel | c.1056N>C | p.Leu352Phe | p.L352F | Q9UJX2 | protein_coding | deleterious(0.03) | probably_damaging(0.937) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
| CDC23 | SNV | Missense_Mutation | rs374640902 | c.449N>T | p.Ala150Val | p.A150V | Q9UJX2 | protein_coding | tolerated(0.49) | benign(0.005) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
| 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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