![]() |
|||||
|
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() | |
![]() |
Gene: CDCA7L |
Gene summary for CDCA7L |
![]() |
Gene information | Species | Human | Gene symbol | CDCA7L | Gene ID | 55536 |
Gene name | cell division cycle associated 7 like | |
Gene Alias | JPO2 | |
Cytomap | 7p15.3 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | Q96GN5 |
Top |
Malignant transformation analysis |
![]() |
![]() |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55536 | CDCA7L | LZE2T | Human | Esophagus | ESCC | 3.88e-03 | 3.51e-01 | 0.082 |
55536 | CDCA7L | LZE4T | Human | Esophagus | ESCC | 5.79e-09 | 1.97e-01 | 0.0811 |
55536 | CDCA7L | LZE5T | Human | Esophagus | ESCC | 1.57e-02 | 1.87e-01 | 0.0514 |
55536 | CDCA7L | LZE7T | Human | Esophagus | ESCC | 6.70e-04 | 3.66e-01 | 0.0667 |
55536 | CDCA7L | LZE8T | Human | Esophagus | ESCC | 2.60e-05 | 1.47e-01 | 0.067 |
55536 | CDCA7L | LZE24T | Human | Esophagus | ESCC | 3.65e-12 | 3.45e-01 | 0.0596 |
55536 | CDCA7L | LZE21T | Human | Esophagus | ESCC | 4.63e-04 | 3.65e-01 | 0.0655 |
55536 | CDCA7L | LZE6T | Human | Esophagus | ESCC | 4.70e-07 | 3.04e-01 | 0.0845 |
55536 | CDCA7L | P1T-E | Human | Esophagus | ESCC | 4.64e-10 | 5.92e-01 | 0.0875 |
55536 | CDCA7L | P2T-E | Human | Esophagus | ESCC | 3.77e-37 | 7.50e-01 | 0.1177 |
55536 | CDCA7L | P4T-E | Human | Esophagus | ESCC | 1.64e-13 | 4.06e-01 | 0.1323 |
55536 | CDCA7L | P5T-E | Human | Esophagus | ESCC | 7.19e-18 | 4.18e-01 | 0.1327 |
55536 | CDCA7L | P8T-E | Human | Esophagus | ESCC | 4.66e-38 | 6.75e-01 | 0.0889 |
55536 | CDCA7L | P9T-E | Human | Esophagus | ESCC | 2.82e-12 | 3.77e-01 | 0.1131 |
55536 | CDCA7L | P10T-E | Human | Esophagus | ESCC | 3.76e-58 | 1.10e+00 | 0.116 |
55536 | CDCA7L | P11T-E | Human | Esophagus | ESCC | 8.22e-12 | 6.10e-01 | 0.1426 |
55536 | CDCA7L | P12T-E | Human | Esophagus | ESCC | 4.50e-29 | 5.68e-01 | 0.1122 |
55536 | CDCA7L | P15T-E | Human | Esophagus | ESCC | 6.53e-31 | 6.88e-01 | 0.1149 |
55536 | CDCA7L | P16T-E | Human | Esophagus | ESCC | 3.00e-42 | 5.72e-01 | 0.1153 |
55536 | CDCA7L | P17T-E | Human | Esophagus | ESCC | 2.68e-18 | 3.92e-01 | 0.1278 |
Page: 1 2 3 4 5 6 |
![]() |
∗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. |
Top |
Malignant transformation related pathway analysis |
![]() |
![]() |
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 |
![]() |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
Page: 1 |
![]() |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
Page: 1 |
Top |
Cell-cell communication analysis |
![]() |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
Page: 1 |
Top |
Single-cell gene regulatory network inference analysis |
![]() |
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 |
Top |
Somatic mutation of malignant transformation related genes |
![]() |
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 |
CDCA7L | SNV | Missense_Mutation | c.622N>A | p.Gln208Lys | p.Q208K | Q96GN5 | protein_coding | deleterious(0.01) | benign(0.095) | TCGA-A8-A09A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD | |
CDCA7L | SNV | Missense_Mutation | c.1216N>A | p.Cys406Ser | p.C406S | Q96GN5 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AO-A0J2-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD | |
CDCA7L | SNV | Missense_Mutation | c.818G>A | p.Arg273Gln | p.R273Q | Q96GN5 | protein_coding | deleterious(0.01) | probably_damaging(0.996) | TCGA-E2-A14V-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | cyclophosphamide | SD | |
CDCA7L | deletion | Frame_Shift_Del | novel | c.1075_1076delNN | p.Lys359AspfsTer60 | p.K359Dfs*60 | Q96GN5 | protein_coding | TCGA-AR-A1AY-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unspecific | Doxorubicin | SD | ||
CDCA7L | SNV | Missense_Mutation | c.866N>T | p.Ser289Leu | p.S289L | Q96GN5 | protein_coding | tolerated(0.08) | probably_damaging(0.994) | TCGA-EK-A2PG-01 | Cervix | cervical & endocervical cancer | Female | >=65 | I/II | Unknown | Unknown | SD | |
CDCA7L | SNV | Missense_Mutation | rs749525504 | c.55G>A | p.Ala19Thr | p.A19T | Q96GN5 | protein_coding | tolerated(0.1) | possibly_damaging(0.683) | TCGA-AA-3492-01 | Colorectum | colon adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CDCA7L | SNV | Missense_Mutation | c.976N>A | p.Glu326Lys | p.E326K | Q96GN5 | protein_coding | tolerated(0.09) | benign(0.009) | TCGA-AA-3663-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
CDCA7L | SNV | Missense_Mutation | c.376G>T | p.Asp126Tyr | p.D126Y | Q96GN5 | protein_coding | deleterious(0.03) | benign(0.04) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
CDCA7L | SNV | Missense_Mutation | rs770755131 | c.710N>T | p.Ser237Leu | p.S237L | Q96GN5 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-AA-A00N-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
CDCA7L | SNV | Missense_Mutation | rs770218756 | c.538N>A | p.Leu180Ile | p.L180I | Q96GN5 | protein_coding | tolerated(0.13) | benign(0.005) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
Page: 1 2 3 4 5 6 7 |
Top |
Related drugs of malignant transformation related genes |
![]() |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
Page: 1 |