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Gene: CCDC58 |
Gene summary for CCDC58 |
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Gene information | Species | Human | Gene symbol | CCDC58 | Gene ID | 131076 |
Gene name | mitochondrial matrix import factor 23 | |
Gene Alias | CCDC58 | |
Cytomap | 3q21.1 | |
Gene Type | protein-coding | GO ID | GO:0005575 | UniProtAcc | Q4VC31 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
131076 | CCDC58 | LZE2T | Human | Esophagus | ESCC | 2.38e-03 | 8.29e-01 | 0.082 |
131076 | CCDC58 | LZE4T | Human | Esophagus | ESCC | 4.06e-11 | 4.43e-01 | 0.0811 |
131076 | CCDC58 | LZE7T | Human | Esophagus | ESCC | 1.07e-10 | 5.56e-01 | 0.0667 |
131076 | CCDC58 | LZE8T | Human | Esophagus | ESCC | 4.45e-03 | 1.69e-01 | 0.067 |
131076 | CCDC58 | LZE22T | Human | Esophagus | ESCC | 2.19e-06 | 3.51e-01 | 0.068 |
131076 | CCDC58 | LZE24T | Human | Esophagus | ESCC | 1.30e-08 | 2.60e-01 | 0.0596 |
131076 | CCDC58 | LZE21T | Human | Esophagus | ESCC | 9.13e-06 | 5.93e-01 | 0.0655 |
131076 | CCDC58 | P1T-E | Human | Esophagus | ESCC | 5.99e-08 | 4.62e-01 | 0.0875 |
131076 | CCDC58 | P2T-E | Human | Esophagus | ESCC | 3.30e-09 | 2.18e-01 | 0.1177 |
131076 | CCDC58 | P4T-E | Human | Esophagus | ESCC | 5.65e-31 | 9.10e-01 | 0.1323 |
131076 | CCDC58 | P5T-E | Human | Esophagus | ESCC | 1.56e-56 | 1.11e+00 | 0.1327 |
131076 | CCDC58 | P8T-E | Human | Esophagus | ESCC | 2.53e-19 | 3.37e-01 | 0.0889 |
131076 | CCDC58 | P9T-E | Human | Esophagus | ESCC | 4.22e-25 | 6.70e-01 | 0.1131 |
131076 | CCDC58 | P10T-E | Human | Esophagus | ESCC | 1.01e-48 | 7.44e-01 | 0.116 |
131076 | CCDC58 | P11T-E | Human | Esophagus | ESCC | 2.97e-04 | 2.99e-01 | 0.1426 |
131076 | CCDC58 | P12T-E | Human | Esophagus | ESCC | 1.22e-26 | 5.99e-01 | 0.1122 |
131076 | CCDC58 | P15T-E | Human | Esophagus | ESCC | 8.52e-23 | 4.80e-01 | 0.1149 |
131076 | CCDC58 | P16T-E | Human | Esophagus | ESCC | 5.09e-25 | 6.05e-01 | 0.1153 |
131076 | CCDC58 | P17T-E | Human | Esophagus | ESCC | 5.27e-05 | 4.58e-01 | 0.1278 |
131076 | CCDC58 | P19T-E | Human | Esophagus | ESCC | 1.62e-05 | 6.81e-01 | 0.1662 |
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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). |
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GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
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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 |
CCDC58 | SNV | Missense_Mutation | c.273N>C | p.Lys91Asn | p.K91N | Q4VC31 | protein_coding | tolerated(0.26) | benign(0.037) | TCGA-IR-A3LL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR | |
CCDC58 | SNV | Missense_Mutation | novel | c.250N>C | p.Asn84His | p.N84H | Q4VC31 | protein_coding | tolerated(0.12) | benign(0.003) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CCDC58 | SNV | Missense_Mutation | c.273G>T | p.Lys91Asn | p.K91N | Q4VC31 | protein_coding | tolerated(0.26) | benign(0.037) | TCGA-A5-A0GP-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
CCDC58 | SNV | Missense_Mutation | novel | c.361N>A | p.Val121Met | p.V121M | Q4VC31 | protein_coding | deleterious(0) | probably_damaging(0.934) | TCGA-A5-A1OF-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CCDC58 | SNV | Missense_Mutation | c.110N>T | p.Thr37Met | p.T37M | Q4VC31 | protein_coding | deleterious(0) | probably_damaging(0.927) | TCGA-AP-A059-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | |
CCDC58 | SNV | Missense_Mutation | novel | c.146C>T | p.Ala49Val | p.A49V | Q4VC31 | protein_coding | tolerated(0.08) | benign(0.311) | TCGA-AP-A1DK-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CCDC58 | SNV | Missense_Mutation | novel | c.86N>T | p.Arg29Ile | p.R29I | Q4VC31 | protein_coding | deleterious(0.04) | probably_damaging(0.944) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CCDC58 | SNV | Missense_Mutation | c.88N>C | p.Ile30Leu | p.I30L | Q4VC31 | protein_coding | deleterious(0.01) | possibly_damaging(0.871) | TCGA-AX-A0J0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
CCDC58 | SNV | Missense_Mutation | c.110C>T | p.Thr37Met | p.T37M | Q4VC31 | protein_coding | deleterious(0) | probably_damaging(0.927) | TCGA-B5-A0JY-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | doxorubicin | SD | |
CCDC58 | SNV | Missense_Mutation | c.31N>C | p.Glu11Gln | p.E11Q | Q4VC31 | protein_coding | tolerated(0.47) | benign(0.287) | TCGA-B5-A11R-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Chemotherapy | paclitaxel | SD |
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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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