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Gene: CDC37L1 |
Gene summary for CDC37L1 |
Gene summary. |
Gene information | Species | Human | Gene symbol | CDC37L1 | Gene ID | 55664 |
Gene name | cell division cycle 37 like 1 | |
Gene Alias | CDC37B | |
Cytomap | 9p24.1 | |
Gene Type | protein-coding | GO ID | GO:0006457 | UniProtAcc | Q7L3B6 |
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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 |
55664 | CDC37L1 | P130T-E | Human | Esophagus | ESCC | 2.76e-34 | 6.13e-01 | 0.1676 |
55664 | CDC37L1 | C04 | Human | Oral cavity | OSCC | 2.50e-04 | 3.61e-01 | 0.2633 |
55664 | CDC37L1 | C21 | Human | Oral cavity | OSCC | 5.96e-04 | 2.34e-01 | 0.2678 |
55664 | CDC37L1 | C30 | Human | Oral cavity | OSCC | 4.32e-20 | 9.60e-01 | 0.3055 |
55664 | CDC37L1 | C38 | Human | Oral cavity | OSCC | 6.26e-10 | 1.20e+00 | 0.172 |
55664 | CDC37L1 | C43 | Human | Oral cavity | OSCC | 1.20e-16 | 3.65e-01 | 0.1704 |
55664 | CDC37L1 | C46 | Human | Oral cavity | OSCC | 1.35e-05 | 2.52e-01 | 0.1673 |
55664 | CDC37L1 | C51 | Human | Oral cavity | OSCC | 7.24e-04 | 2.30e-01 | 0.2674 |
55664 | CDC37L1 | C57 | Human | Oral cavity | OSCC | 2.39e-12 | 4.74e-01 | 0.1679 |
55664 | CDC37L1 | C06 | Human | Oral cavity | OSCC | 1.48e-02 | 5.55e-01 | 0.2699 |
55664 | CDC37L1 | C08 | Human | Oral cavity | OSCC | 2.60e-09 | 1.94e-01 | 0.1919 |
55664 | CDC37L1 | LN22 | Human | Oral cavity | OSCC | 2.05e-07 | 7.84e-01 | 0.1733 |
55664 | CDC37L1 | SYSMH2 | Human | Oral cavity | OSCC | 2.15e-04 | 2.94e-01 | 0.2326 |
55664 | CDC37L1 | SYSMH3 | Human | Oral cavity | OSCC | 8.50e-13 | 3.98e-01 | 0.2442 |
55664 | CDC37L1 | SYSMH6 | Human | Oral cavity | OSCC | 9.18e-03 | 1.99e-01 | 0.1275 |
55664 | CDC37L1 | male-WTA | Human | Thyroid | PTC | 9.78e-15 | 1.33e-01 | 0.1037 |
55664 | CDC37L1 | PTC01 | Human | Thyroid | PTC | 2.64e-06 | 1.69e-01 | 0.1899 |
55664 | CDC37L1 | PTC03 | Human | Thyroid | PTC | 3.45e-02 | 8.37e-02 | 0.1784 |
55664 | CDC37L1 | PTC04 | Human | Thyroid | PTC | 1.75e-06 | 1.95e-01 | 0.1927 |
55664 | CDC37L1 | PTC05 | Human | Thyroid | PTC | 4.73e-13 | 4.90e-01 | 0.2065 |
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Transcriptomic changes along malignancy continuum. |
∗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). |
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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0031647111 | Esophagus | ESCC | regulation of protein stability | 223/8552 | 298/18723 | 5.76e-25 | 1.52e-22 | 223 |
GO:0006457110 | Esophagus | ESCC | protein folding | 163/8552 | 212/18723 | 1.13e-20 | 1.74e-18 | 163 |
GO:0050821111 | Esophagus | ESCC | protein stabilization | 140/8552 | 191/18723 | 6.50e-15 | 3.61e-13 | 140 |
GO:000645718 | Oral cavity | OSCC | protein folding | 154/7305 | 212/18723 | 1.89e-23 | 4.60e-21 | 154 |
GO:003164720 | Oral cavity | OSCC | regulation of protein stability | 193/7305 | 298/18723 | 1.30e-19 | 1.95e-17 | 193 |
GO:005082120 | Oral cavity | OSCC | protein stabilization | 122/7305 | 191/18723 | 2.69e-12 | 1.09e-10 | 122 |
GO:0006457112 | Thyroid | PTC | protein folding | 137/5968 | 212/18723 | 8.29e-23 | 2.01e-20 | 137 |
GO:0031647113 | Thyroid | PTC | regulation of protein stability | 174/5968 | 298/18723 | 2.05e-21 | 4.05e-19 | 174 |
GO:0050821113 | Thyroid | PTC | protein stabilization | 115/5968 | 191/18723 | 5.67e-16 | 4.31e-14 | 115 |
GO:000645733 | Thyroid | ATC | protein folding | 140/6293 | 212/18723 | 3.46e-22 | 8.09e-20 | 140 |
GO:003164734 | Thyroid | ATC | regulation of protein stability | 177/6293 | 298/18723 | 4.08e-20 | 6.46e-18 | 177 |
GO:005082134 | Thyroid | ATC | protein stabilization | 117/6293 | 191/18723 | 3.98e-15 | 2.71e-13 | 117 |
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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 |
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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. |
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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 |
CDC37L1 | SNV | Missense_Mutation | c.164N>G | p.Gln55Arg | p.Q55R | Q7L3B6 | protein_coding | deleterious(0.04) | possibly_damaging(0.78) | TCGA-AN-A0XN-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
CDC37L1 | SNV | Missense_Mutation | c.607N>T | p.His203Tyr | p.H203Y | Q7L3B6 | protein_coding | tolerated(0.1) | possibly_damaging(0.884) | TCGA-BH-A0DL-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cytoxan | CR | |
CDC37L1 | SNV | Missense_Mutation | rs372436527 | c.844N>G | p.Met282Val | p.M282V | Q7L3B6 | protein_coding | tolerated(0.25) | benign(0.003) | TCGA-E2-A14S-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | cytoxan | SD |
CDC37L1 | SNV | Missense_Mutation | novel | c.751N>C | p.Glu251Gln | p.E251Q | Q7L3B6 | protein_coding | tolerated(0.14) | possibly_damaging(0.588) | TCGA-EW-A1J5-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | adriamycin | SD |
CDC37L1 | SNV | Missense_Mutation | rs756219911 | c.725N>A | p.Arg242His | p.R242H | Q7L3B6 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-G4-6317-01 | Colorectum | colon adenocarcinoma | Female | <65 | III/IV | Chemotherapy | fluorouracil | PD |
CDC37L1 | SNV | Missense_Mutation | rs750184463 | c.437N>T | p.Arg146Ile | p.R146I | Q7L3B6 | protein_coding | deleterious(0.04) | benign(0.062) | TCGA-EI-6917-01 | Colorectum | rectum adenocarcinoma | Male | <65 | III/IV | Chemotherapy | 5fluorouracil+oxaciplatina+l-folinian | SD |
CDC37L1 | insertion | Frame_Shift_Ins | novel | c.943_944insCATACATATATATT | p.Ala316TyrfsTer10 | p.A316Yfs*10 | Q7L3B6 | protein_coding | TCGA-AM-5820-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
CDC37L1 | SNV | Missense_Mutation | novel | c.548N>A | p.Ser183Tyr | p.S183Y | Q7L3B6 | protein_coding | deleterious(0) | probably_damaging(0.93) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
CDC37L1 | SNV | Missense_Mutation | novel | c.128N>T | p.Ala43Val | p.A43V | Q7L3B6 | protein_coding | tolerated(0.12) | benign(0.001) | TCGA-A5-A1OG-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Chemotherapy | taxol | PD |
CDC37L1 | SNV | Missense_Mutation | novel | c.889N>A | p.Gly297Ser | p.G297S | Q7L3B6 | protein_coding | tolerated(0.13) | benign(0.14) | TCGA-AJ-A3EK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | carboplatin | CR |
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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 |
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