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Gene: CCDC22 |
Gene summary for CCDC22 |
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Gene information | Species | Human | Gene symbol | CCDC22 | Gene ID | 28952 |
Gene name | coiled-coil domain containing 22 | |
Gene Alias | CXorf37 | |
Cytomap | Xp11.23 | |
Gene Type | protein-coding | GO ID | GO:0006139 | UniProtAcc | A0A024QZ03 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
28952 | CCDC22 | LZE4T | Human | Esophagus | ESCC | 8.05e-03 | 1.33e-01 | 0.0811 |
28952 | CCDC22 | LZE7T | Human | Esophagus | ESCC | 4.68e-02 | 1.84e-01 | 0.0667 |
28952 | CCDC22 | LZE24T | Human | Esophagus | ESCC | 1.00e-06 | 1.27e-01 | 0.0596 |
28952 | CCDC22 | P1T-E | Human | Esophagus | ESCC | 1.52e-03 | 1.55e-01 | 0.0875 |
28952 | CCDC22 | P2T-E | Human | Esophagus | ESCC | 1.91e-11 | 2.73e-01 | 0.1177 |
28952 | CCDC22 | P4T-E | Human | Esophagus | ESCC | 2.86e-14 | 2.25e-01 | 0.1323 |
28952 | CCDC22 | P5T-E | Human | Esophagus | ESCC | 1.18e-05 | 1.20e-01 | 0.1327 |
28952 | CCDC22 | P8T-E | Human | Esophagus | ESCC | 2.63e-18 | 2.88e-01 | 0.0889 |
28952 | CCDC22 | P9T-E | Human | Esophagus | ESCC | 3.43e-08 | 1.60e-01 | 0.1131 |
28952 | CCDC22 | P10T-E | Human | Esophagus | ESCC | 9.82e-09 | 8.83e-02 | 0.116 |
28952 | CCDC22 | P11T-E | Human | Esophagus | ESCC | 9.39e-09 | 2.51e-01 | 0.1426 |
28952 | CCDC22 | P12T-E | Human | Esophagus | ESCC | 3.31e-12 | 2.04e-01 | 0.1122 |
28952 | CCDC22 | P15T-E | Human | Esophagus | ESCC | 1.06e-13 | 2.65e-01 | 0.1149 |
28952 | CCDC22 | P16T-E | Human | Esophagus | ESCC | 1.79e-17 | 1.70e-01 | 0.1153 |
28952 | CCDC22 | P17T-E | Human | Esophagus | ESCC | 1.27e-04 | 2.70e-01 | 0.1278 |
28952 | CCDC22 | P19T-E | Human | Esophagus | ESCC | 1.71e-05 | 3.76e-01 | 0.1662 |
28952 | CCDC22 | P20T-E | Human | Esophagus | ESCC | 4.23e-10 | 1.91e-01 | 0.1124 |
28952 | CCDC22 | P21T-E | Human | Esophagus | ESCC | 6.61e-12 | 1.92e-01 | 0.1617 |
28952 | CCDC22 | P22T-E | Human | Esophagus | ESCC | 2.06e-08 | 1.03e-01 | 0.1236 |
28952 | CCDC22 | P23T-E | Human | Esophagus | ESCC | 6.07e-20 | 4.68e-01 | 0.108 |
Page: 1 2 3 4 |
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∗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). |
Page: 1 2 3 4 5 6 7 8 9 |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:004819318 | Esophagus | ESCC | Golgi vesicle transport | 231/8552 | 296/18723 | 1.82e-30 | 9.63e-28 | 231 |
GO:0042176111 | Esophagus | ESCC | regulation of protein catabolic process | 280/8552 | 391/18723 | 8.65e-26 | 2.39e-23 | 280 |
GO:0009896111 | Esophagus | ESCC | positive regulation of catabolic process | 332/8552 | 492/18723 | 4.36e-23 | 9.22e-21 | 332 |
GO:0031331111 | Esophagus | ESCC | positive regulation of cellular catabolic process | 292/8552 | 427/18723 | 8.67e-22 | 1.53e-19 | 292 |
GO:1903362111 | Esophagus | ESCC | regulation of cellular protein catabolic process | 188/8552 | 255/18723 | 5.12e-20 | 6.62e-18 | 188 |
GO:0045862111 | Esophagus | ESCC | positive regulation of proteolysis | 256/8552 | 372/18723 | 7.88e-20 | 9.43e-18 | 256 |
GO:1903050111 | Esophagus | ESCC | regulation of proteolysis involved in cellular protein catabolic process | 163/8552 | 221/18723 | 1.44e-17 | 1.27e-15 | 163 |
GO:001619715 | Esophagus | ESCC | endosomal transport | 168/8552 | 230/18723 | 2.28e-17 | 1.93e-15 | 168 |
GO:0045732111 | Esophagus | ESCC | positive regulation of protein catabolic process | 167/8552 | 231/18723 | 1.47e-16 | 1.14e-14 | 167 |
GO:2000058111 | Esophagus | ESCC | regulation of ubiquitin-dependent protein catabolic process | 125/8552 | 164/18723 | 1.17e-15 | 7.76e-14 | 125 |
GO:1903364111 | Esophagus | ESCC | positive regulation of cellular protein catabolic process | 117/8552 | 155/18723 | 3.25e-14 | 1.66e-12 | 117 |
GO:1903052110 | Esophagus | ESCC | positive regulation of proteolysis involved in cellular protein catabolic process | 101/8552 | 133/18723 | 9.58e-13 | 4.19e-11 | 101 |
GO:004312318 | Esophagus | ESCC | positive regulation of I-kappaB kinase/NF-kappaB signaling | 132/8552 | 186/18723 | 2.07e-12 | 8.58e-11 | 132 |
GO:000689215 | Esophagus | ESCC | post-Golgi vesicle-mediated transport | 82/8552 | 104/18723 | 4.00e-12 | 1.55e-10 | 82 |
GO:0043122110 | Esophagus | ESCC | regulation of I-kappaB kinase/NF-kappaB signaling | 167/8552 | 249/18723 | 6.11e-12 | 2.32e-10 | 167 |
GO:000724919 | Esophagus | ESCC | I-kappaB kinase/NF-kappaB signaling | 183/8552 | 281/18723 | 3.02e-11 | 1.01e-09 | 183 |
GO:009887615 | Esophagus | ESCC | vesicle-mediated transport to the plasma membrane | 99/8552 | 136/18723 | 1.13e-10 | 3.39e-09 | 99 |
GO:2000060111 | Esophagus | ESCC | positive regulation of ubiquitin-dependent protein catabolic process | 81/8552 | 107/18723 | 2.23e-10 | 6.34e-09 | 81 |
GO:0045185111 | Esophagus | ESCC | maintenance of protein location | 71/8552 | 94/18723 | 3.41e-09 | 7.24e-08 | 71 |
GO:0051235110 | Esophagus | ESCC | maintenance of location | 200/8552 | 327/18723 | 1.01e-08 | 2.02e-07 | 200 |
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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 |
CCDC22 | SNV | Missense_Mutation | novel | c.1273N>T | p.Arg425Trp | p.R425W | O60826 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-CC-A7IL-01 | Liver | liver hepatocellular carcinoma | Male | <65 | III/IV | Unknown | Unknown | PD |
CCDC22 | SNV | Missense_Mutation | novel | c.71A>T | p.Gln24Leu | p.Q24L | O60826 | protein_coding | tolerated(0.09) | possibly_damaging(0.871) | TCGA-97-A4LX-01 | Lung | lung adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
CCDC22 | SNV | Missense_Mutation | novel | c.1697N>G | p.Asn566Ser | p.N566S | O60826 | protein_coding | tolerated(0.07) | probably_damaging(0.998) | TCGA-MN-A4N5-01 | Lung | lung adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
CCDC22 | SNV | Missense_Mutation | novel | c.1036N>A | p.Arg346Ser | p.R346S | O60826 | protein_coding | tolerated(0.83) | benign(0.006) | TCGA-21-1076-01 | Lung | lung squamous cell carcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
CCDC22 | SNV | Missense_Mutation | c.416N>A | p.Ala139Glu | p.A139E | O60826 | protein_coding | tolerated(0.29) | probably_damaging(0.911) | TCGA-EJ-5514-01 | Prostate | prostate adenocarcinoma | Male | >=65 | 9 | Unknown | Unknown | SD | |
CCDC22 | SNV | Missense_Mutation | rs201055378 | c.143C>T | p.Ala48Val | p.A48V | O60826 | protein_coding | tolerated(0.2) | benign(0.137) | TCGA-BR-4361-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
CCDC22 | SNV | Missense_Mutation | c.1181N>T | p.Pro394Leu | p.P394L | O60826 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-CG-4301-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD | |
CCDC22 | SNV | Missense_Mutation | novel | c.187G>A | p.Ala63Thr | p.A63T | O60826 | protein_coding | deleterious(0) | possibly_damaging(0.905) | TCGA-D7-A6EY-01 | Stomach | stomach adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD |
CCDC22 | SNV | Missense_Mutation | novel | c.1762G>A | p.Glu588Lys | p.E588K | O60826 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-VQ-A8P2-01 | Stomach | stomach adenocarcinoma | Male | >=65 | III/IV | Unspecific | Complete Response |
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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 |
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