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Gene: CLDN7 |
Gene summary for CLDN7 |
Gene summary. |
Gene information | Species | Human | Gene symbol | CLDN7 | Gene ID | 1366 |
Gene name | claudin 7 | |
Gene Alias | CEPTRL2 | |
Cytomap | 17p13.1 | |
Gene Type | protein-coding | GO ID | GO:0007043 | UniProtAcc | O95471 |
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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 |
1366 | CLDN7 | GSM4909282 | Human | Breast | IDC | 1.08e-05 | -4.13e-01 | -0.0288 |
1366 | CLDN7 | GSM4909286 | Human | Breast | IDC | 8.96e-24 | -6.51e-01 | 0.1081 |
1366 | CLDN7 | GSM4909287 | Human | Breast | IDC | 4.90e-08 | -4.39e-01 | 0.2057 |
1366 | CLDN7 | GSM4909288 | Human | Breast | IDC | 4.01e-07 | -6.68e-01 | 0.0988 |
1366 | CLDN7 | GSM4909290 | Human | Breast | IDC | 9.90e-07 | -3.52e-01 | 0.2096 |
1366 | CLDN7 | GSM4909292 | Human | Breast | IDC | 1.10e-03 | -7.32e-01 | 0.1236 |
1366 | CLDN7 | GSM4909293 | Human | Breast | IDC | 4.27e-07 | -2.66e-01 | 0.1581 |
1366 | CLDN7 | GSM4909294 | Human | Breast | IDC | 3.36e-12 | -4.84e-01 | 0.2022 |
1366 | CLDN7 | GSM4909296 | Human | Breast | IDC | 2.70e-12 | -2.96e-01 | 0.1524 |
1366 | CLDN7 | GSM4909297 | Human | Breast | IDC | 6.30e-20 | 8.01e-02 | 0.1517 |
1366 | CLDN7 | GSM4909308 | Human | Breast | IDC | 4.95e-08 | -2.89e-01 | 0.158 |
1366 | CLDN7 | GSM4909311 | Human | Breast | IDC | 3.26e-40 | -5.29e-01 | 0.1534 |
1366 | CLDN7 | GSM4909312 | Human | Breast | IDC | 4.74e-15 | -2.75e-01 | 0.1552 |
1366 | CLDN7 | GSM4909319 | Human | Breast | IDC | 5.72e-46 | -5.08e-01 | 0.1563 |
1366 | CLDN7 | GSM4909320 | Human | Breast | IDC | 3.25e-03 | -2.65e-01 | 0.1575 |
1366 | CLDN7 | GSM4909321 | Human | Breast | IDC | 1.85e-13 | 2.84e-02 | 0.1559 |
1366 | CLDN7 | brca1 | Human | Breast | Precancer | 1.97e-44 | 7.27e-01 | -0.0338 |
1366 | CLDN7 | brca2 | Human | Breast | Precancer | 8.09e-15 | 4.24e-01 | -0.024 |
1366 | CLDN7 | brca3 | Human | Breast | Precancer | 1.24e-32 | 6.26e-01 | -0.0263 |
1366 | CLDN7 | M1 | Human | Breast | IDC | 6.12e-05 | -4.18e-01 | 0.1577 |
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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:00452169 | Cervix | CC | cell-cell junction organization | 53/2311 | 200/18723 | 3.83e-08 | 2.53e-06 | 53 |
GO:00343298 | Cervix | CC | cell junction assembly | 88/2311 | 420/18723 | 3.42e-07 | 1.38e-05 | 88 |
GO:00070439 | Cervix | CC | cell-cell junction assembly | 39/2311 | 146/18723 | 1.86e-06 | 5.94e-05 | 39 |
GO:00432978 | Cervix | CC | apical junction assembly | 24/2311 | 78/18723 | 1.36e-05 | 2.73e-04 | 24 |
GO:01201927 | Cervix | CC | tight junction assembly | 21/2311 | 74/18723 | 1.69e-04 | 2.00e-03 | 21 |
GO:01201937 | Cervix | CC | tight junction organization | 22/2311 | 80/18723 | 1.97e-04 | 2.26e-03 | 22 |
GO:00708306 | Cervix | CC | bicellular tight junction assembly | 18/2311 | 70/18723 | 1.69e-03 | 1.29e-02 | 18 |
GO:004521614 | Cervix | HSIL_HPV | cell-cell junction organization | 23/737 | 200/18723 | 4.21e-06 | 1.69e-04 | 23 |
GO:000704314 | Cervix | HSIL_HPV | cell-cell junction assembly | 19/737 | 146/18723 | 4.72e-06 | 1.84e-04 | 19 |
GO:004329714 | Cervix | HSIL_HPV | apical junction assembly | 11/737 | 78/18723 | 2.29e-04 | 4.03e-03 | 11 |
GO:007083013 | Cervix | HSIL_HPV | bicellular tight junction assembly | 10/737 | 70/18723 | 3.94e-04 | 6.10e-03 | 10 |
GO:012019213 | Cervix | HSIL_HPV | tight junction assembly | 10/737 | 74/18723 | 6.19e-04 | 8.62e-03 | 10 |
GO:012019313 | Cervix | HSIL_HPV | tight junction organization | 10/737 | 80/18723 | 1.15e-03 | 1.38e-02 | 10 |
GO:003432913 | Cervix | HSIL_HPV | cell junction assembly | 28/737 | 420/18723 | 4.82e-03 | 3.98e-02 | 28 |
GO:004521624 | Cervix | N_HPV | cell-cell junction organization | 15/534 | 200/18723 | 6.41e-04 | 8.27e-03 | 15 |
GO:0098742 | Cervix | N_HPV | cell-cell adhesion via plasma-membrane adhesion molecules | 17/534 | 273/18723 | 2.26e-03 | 2.11e-02 | 17 |
GO:000704323 | Cervix | N_HPV | cell-cell junction assembly | 11/534 | 146/18723 | 3.15e-03 | 2.64e-02 | 11 |
GO:012019323 | Cervix | N_HPV | tight junction organization | 7/534 | 80/18723 | 7.80e-03 | 4.97e-02 | 7 |
GO:0045216 | Colorectum | AD | cell-cell junction organization | 80/3918 | 200/18723 | 5.57e-10 | 4.58e-08 | 80 |
GO:0034329 | Colorectum | AD | cell junction assembly | 136/3918 | 420/18723 | 2.02e-08 | 1.15e-06 | 136 |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa051604 | Stomach | CAG with IM | Hepatitis C | 21/640 | 157/8465 | 7.26e-03 | 4.05e-02 | 2.84e-02 | 21 |
hsa0513031 | Stomach | CAG with IM | Pathogenic Escherichia coli infection | 41/640 | 197/8465 | 1.58e-09 | 3.13e-08 | 2.20e-08 | 41 |
hsa0453031 | Stomach | CAG with IM | Tight junction | 32/640 | 169/8465 | 9.69e-07 | 1.62e-05 | 1.14e-05 | 32 |
hsa0467031 | Stomach | CAG with IM | Leukocyte transendothelial migration | 22/640 | 114/8465 | 3.55e-05 | 4.03e-04 | 2.83e-04 | 22 |
hsa045143 | Stomach | CAG with IM | Cell adhesion molecules | 23/640 | 157/8465 | 1.57e-03 | 1.02e-02 | 7.16e-03 | 23 |
hsa0516011 | Stomach | CAG with IM | Hepatitis C | 21/640 | 157/8465 | 7.26e-03 | 4.05e-02 | 2.84e-02 | 21 |
hsa0513041 | Stomach | CSG | Pathogenic Escherichia coli infection | 40/633 | 197/8465 | 3.88e-09 | 7.67e-08 | 5.52e-08 | 40 |
hsa0453041 | Stomach | CSG | Tight junction | 31/633 | 169/8465 | 2.29e-06 | 3.45e-05 | 2.48e-05 | 31 |
hsa0467041 | Stomach | CSG | Leukocyte transendothelial migration | 21/633 | 114/8465 | 9.19e-05 | 9.37e-04 | 6.74e-04 | 21 |
hsa045144 | Stomach | CSG | Cell adhesion molecules | 22/633 | 157/8465 | 3.03e-03 | 1.88e-02 | 1.35e-02 | 22 |
hsa0513051 | Stomach | CSG | Pathogenic Escherichia coli infection | 40/633 | 197/8465 | 3.88e-09 | 7.67e-08 | 5.52e-08 | 40 |
hsa0453051 | Stomach | CSG | Tight junction | 31/633 | 169/8465 | 2.29e-06 | 3.45e-05 | 2.48e-05 | 31 |
hsa0467051 | Stomach | CSG | Leukocyte transendothelial migration | 21/633 | 114/8465 | 9.19e-05 | 9.37e-04 | 6.74e-04 | 21 |
hsa045145 | Stomach | CSG | Cell adhesion molecules | 22/633 | 157/8465 | 3.03e-03 | 1.88e-02 | 1.35e-02 | 22 |
hsa0513081 | Stomach | WIM | Pathogenic Escherichia coli infection | 22/284 | 197/8465 | 6.52e-07 | 1.07e-05 | 8.55e-06 | 22 |
hsa0467081 | Stomach | WIM | Leukocyte transendothelial migration | 12/284 | 114/8465 | 4.20e-04 | 4.35e-03 | 3.47e-03 | 12 |
hsa0453081 | Stomach | WIM | Tight junction | 13/284 | 169/8465 | 4.42e-03 | 3.10e-02 | 2.47e-02 | 13 |
hsa0513091 | Stomach | WIM | Pathogenic Escherichia coli infection | 22/284 | 197/8465 | 6.52e-07 | 1.07e-05 | 8.55e-06 | 22 |
hsa0467091 | Stomach | WIM | Leukocyte transendothelial migration | 12/284 | 114/8465 | 4.20e-04 | 4.35e-03 | 3.47e-03 | 12 |
hsa0453091 | Stomach | WIM | Tight junction | 13/284 | 169/8465 | 4.42e-03 | 3.10e-02 | 2.47e-02 | 13 |
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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 |
CLDN7 | SNV | Missense_Mutation | novel | c.232N>G | p.Gln78Glu | p.Q78E | O95471 | protein_coding | deleterious(0) | probably_damaging(0.987) | TCGA-C5-A2LZ-01 | Cervix | cervical & endocervical cancer | Female | >=65 | III/IV | Unknown | Unknown | PD |
CLDN7 | SNV | Missense_Mutation | c.439N>T | p.Asp147Tyr | p.D147Y | O95471 | protein_coding | deleterious(0) | probably_damaging(0.961) | TCGA-AA-3977-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
CLDN7 | SNV | Missense_Mutation | novel | c.373N>C | p.Ile125Leu | p.I125L | O95471 | protein_coding | tolerated(0.53) | benign(0.053) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CLDN7 | SNV | Missense_Mutation | rs773251272 | c.596N>A | p.Arg199His | p.R199H | O95471 | protein_coding | tolerated(0.13) | benign(0.107) | TCGA-WS-AB45-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CLDN7 | SNV | Missense_Mutation | novel | c.345N>T | p.Lys115Asn | p.K115N | O95471 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CLDN7 | SNV | Missense_Mutation | novel | c.227N>T | p.Ala76Val | p.A76V | O95471 | protein_coding | tolerated(0.34) | benign(0.185) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
CLDN7 | SNV | Missense_Mutation | novel | c.373N>G | p.Ile125Val | p.I125V | O95471 | protein_coding | tolerated(0.42) | benign(0.003) | TCGA-B5-A1MR-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
CLDN7 | SNV | Missense_Mutation | novel | c.160N>C | p.Cys54Arg | p.C54R | O95471 | protein_coding | tolerated(0.05) | probably_damaging(0.999) | TCGA-BG-A222-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CLDN7 | SNV | Missense_Mutation | novel | c.382N>A | p.Val128Met | p.V128M | O95471 | protein_coding | tolerated(0.1) | benign(0.409) | TCGA-DF-A2KN-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | Unknown | I/II | Unknown | Unknown | SD |
CLDN7 | SNV | Missense_Mutation | novel | c.80T>C | p.Ile27Thr | p.I27T | O95471 | protein_coding | tolerated(0.08) | benign(0.159) | TCGA-21-1076-01 | Lung | lung squamous cell carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
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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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