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Gene: NCAPD3 |
Gene summary for NCAPD3 |
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Gene information | Species | Human | Gene symbol | NCAPD3 | Gene ID | 23310 |
Gene name | non-SMC condensin II complex subunit D3 | |
Gene Alias | CAP-D3 | |
Cytomap | 11q25 | |
Gene Type | protein-coding | GO ID | GO:0000003 | UniProtAcc | P42695 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
23310 | NCAPD3 | LZE7T | Human | Esophagus | ESCC | 2.89e-04 | 3.01e-01 | 0.0667 |
23310 | NCAPD3 | LZE20T | Human | Esophagus | ESCC | 1.84e-02 | 1.02e-01 | 0.0662 |
23310 | NCAPD3 | LZE24T | Human | Esophagus | ESCC | 1.11e-06 | 1.82e-01 | 0.0596 |
23310 | NCAPD3 | P1T-E | Human | Esophagus | ESCC | 1.04e-02 | 2.05e-01 | 0.0875 |
23310 | NCAPD3 | P2T-E | Human | Esophagus | ESCC | 9.52e-09 | 1.83e-01 | 0.1177 |
23310 | NCAPD3 | P4T-E | Human | Esophagus | ESCC | 2.78e-23 | 6.60e-01 | 0.1323 |
23310 | NCAPD3 | P5T-E | Human | Esophagus | ESCC | 1.56e-05 | 1.58e-01 | 0.1327 |
23310 | NCAPD3 | P8T-E | Human | Esophagus | ESCC | 1.51e-11 | 2.28e-01 | 0.0889 |
23310 | NCAPD3 | P9T-E | Human | Esophagus | ESCC | 1.07e-04 | 1.72e-01 | 0.1131 |
23310 | NCAPD3 | P10T-E | Human | Esophagus | ESCC | 3.33e-17 | 3.71e-01 | 0.116 |
23310 | NCAPD3 | P12T-E | Human | Esophagus | ESCC | 1.29e-16 | 2.30e-01 | 0.1122 |
23310 | NCAPD3 | P15T-E | Human | Esophagus | ESCC | 2.97e-06 | 1.69e-01 | 0.1149 |
23310 | NCAPD3 | P16T-E | Human | Esophagus | ESCC | 2.42e-11 | 2.36e-01 | 0.1153 |
23310 | NCAPD3 | P19T-E | Human | Esophagus | ESCC | 5.24e-04 | 2.97e-01 | 0.1662 |
23310 | NCAPD3 | P20T-E | Human | Esophagus | ESCC | 1.17e-05 | 9.10e-02 | 0.1124 |
23310 | NCAPD3 | P21T-E | Human | Esophagus | ESCC | 7.55e-14 | 3.58e-01 | 0.1617 |
23310 | NCAPD3 | P22T-E | Human | Esophagus | ESCC | 6.61e-08 | 1.52e-01 | 0.1236 |
23310 | NCAPD3 | P23T-E | Human | Esophagus | ESCC | 5.95e-05 | 1.39e-01 | 0.108 |
23310 | NCAPD3 | P24T-E | Human | Esophagus | ESCC | 3.36e-04 | 1.32e-01 | 0.1287 |
23310 | NCAPD3 | P26T-E | Human | Esophagus | ESCC | 1.69e-09 | 2.27e-01 | 0.1276 |
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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:014001414 | Esophagus | ESCC | mitotic nuclear division | 218/8552 | 287/18723 | 6.17e-26 | 1.78e-23 | 218 |
GO:000007011 | Esophagus | ESCC | mitotic sister chromatid segregation | 138/8552 | 168/18723 | 1.37e-22 | 2.63e-20 | 138 |
GO:00008194 | Esophagus | ESCC | sister chromatid segregation | 157/8552 | 202/18723 | 8.41e-21 | 1.33e-18 | 157 |
GO:000705911 | Esophagus | ESCC | chromosome segregation | 238/8552 | 346/18723 | 1.72e-18 | 1.82e-16 | 238 |
GO:00482853 | Esophagus | ESCC | organelle fission | 301/8552 | 488/18723 | 4.64e-13 | 2.12e-11 | 301 |
GO:00988133 | Esophagus | ESCC | nuclear chromosome segregation | 187/8552 | 281/18723 | 1.00e-12 | 4.36e-11 | 187 |
GO:00002802 | Esophagus | ESCC | nuclear division | 270/8552 | 439/18723 | 1.17e-11 | 4.24e-10 | 270 |
GO:00070761 | Esophagus | ESCC | mitotic chromosome condensation | 15/8552 | 17/18723 | 3.48e-04 | 2.03e-03 | 15 |
GO:01400145 | Oral cavity | OSCC | mitotic nuclear division | 191/7305 | 287/18723 | 1.99e-21 | 3.70e-19 | 191 |
GO:00000702 | Oral cavity | OSCC | mitotic sister chromatid segregation | 118/7305 | 168/18723 | 1.89e-16 | 1.48e-14 | 118 |
GO:00008193 | Oral cavity | OSCC | sister chromatid segregation | 135/7305 | 202/18723 | 8.88e-16 | 6.52e-14 | 135 |
GO:00070592 | Oral cavity | OSCC | chromosome segregation | 206/7305 | 346/18723 | 5.82e-15 | 3.76e-13 | 206 |
GO:00482852 | Oral cavity | OSCC | organelle fission | 265/7305 | 488/18723 | 3.22e-12 | 1.27e-10 | 265 |
GO:00002801 | Oral cavity | OSCC | nuclear division | 237/7305 | 439/18723 | 9.62e-11 | 2.90e-09 | 237 |
GO:00988132 | Oral cavity | OSCC | nuclear chromosome segregation | 162/7305 | 281/18723 | 1.56e-10 | 4.56e-09 | 162 |
GO:0007076 | Oral cavity | OSCC | mitotic chromosome condensation | 13/7305 | 17/18723 | 1.92e-03 | 8.94e-03 | 13 |
GO:01400144 | Prostate | BPH | mitotic nuclear division | 67/3107 | 287/18723 | 1.87e-03 | 1.07e-02 | 67 |
GO:014001412 | Prostate | Tumor | mitotic nuclear division | 66/3246 | 287/18723 | 8.19e-03 | 3.60e-02 | 66 |
GO:01400148 | Thyroid | PTC | mitotic nuclear division | 135/5968 | 287/18723 | 4.90e-08 | 1.04e-06 | 135 |
GO:00000705 | Thyroid | PTC | mitotic sister chromatid segregation | 79/5968 | 168/18723 | 2.78e-05 | 2.71e-04 | 79 |
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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 |
NCAPD3 | SNV | Missense_Mutation | novel | c.2222N>T | p.Trp741Leu | p.W741L | P42695 | protein_coding | deleterious(0) | possibly_damaging(0.873) | TCGA-55-8616-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
NCAPD3 | SNV | Missense_Mutation | c.1903N>T | p.Val635Leu | p.V635L | P42695 | protein_coding | deleterious(0) | probably_damaging(0.963) | TCGA-75-5125-01 | Lung | lung adenocarcinoma | Male | Unknown | I/II | Unknown | Unknown | PD | |
NCAPD3 | SNV | Missense_Mutation | novel | c.843G>T | p.Leu281Phe | p.L281F | P42695 | protein_coding | deleterious(0.05) | possibly_damaging(0.53) | TCGA-78-7147-01 | Lung | lung adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD |
NCAPD3 | SNV | Missense_Mutation | c.1156C>T | p.Pro386Ser | p.P386S | P42695 | protein_coding | tolerated(0.06) | benign(0.209) | TCGA-93-A4JQ-01 | Lung | lung adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
NCAPD3 | SNV | Missense_Mutation | c.4240N>G | p.Ser1414Gly | p.S1414G | P42695 | protein_coding | deleterious(0) | probably_damaging(0.996) | TCGA-95-7039-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD | |
NCAPD3 | SNV | Missense_Mutation | rs746992785 | c.2045N>T | p.Ser682Ile | p.S682I | P42695 | protein_coding | tolerated(0.11) | possibly_damaging(0.828) | TCGA-95-7039-01 | Lung | lung adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | PD |
NCAPD3 | SNV | Missense_Mutation | c.2128A>T | p.Thr710Ser | p.T710S | P42695 | protein_coding | deleterious(0.03) | benign(0.124) | TCGA-97-A4M3-01 | Lung | lung adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
NCAPD3 | SNV | Missense_Mutation | novel | c.1084N>T | p.Ala362Ser | p.A362S | P42695 | protein_coding | tolerated(0.12) | benign(0.035) | TCGA-99-AA5R-01 | Lung | lung adenocarcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NCAPD3 | SNV | Missense_Mutation | novel | c.179N>C | p.Ser60Thr | p.S60T | P42695 | protein_coding | tolerated(0.24) | benign(0.053) | TCGA-MN-A4N1-01 | Lung | lung adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
NCAPD3 | SNV | Missense_Mutation | novel | c.4218N>T | p.Glu1406Asp | p.E1406D | P42695 | protein_coding | tolerated(0.63) | benign(0) | TCGA-21-1080-01 | Lung | lung squamous cell carcinoma | Male | >=65 | I/II | Unknown | Unknown | 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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