Tissue | Expression Dynamics | Abbreviation |
Colorectum (GSE201348) | ![The image shows the 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.](images/deg_images/Colorectum/Becker/CHP2_pca_on_diff_genes.png) | FAP: Familial adenomatous polyposis |
CRC: Colorectal cancer |
Colorectum (HTA11) | ![The image shows the 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.](images/deg_images/Colorectum/Chen/CHP2_pca_on_diff_genes.png) | AD: Adenomas |
SER: Sessile serrated lesions |
MSI-H: Microsatellite-high colorectal cancer |
MSS: Microsatellite stable colorectal cancer |
GC | ![The image shows the 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.](images/deg_images/GC/CHP2_pca_on_diff_genes.png) | CAG: Chronic atrophic gastritis |
CAG with IM: Chronic atrophic gastritis with intestinal metaplasia |
CSG: Chronic superficial gastritis |
GC: Gastric cancer |
SIM: Severe intestinal metaplasia |
WIM: Wild intestinal metaplasia |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:0051592 | Colorectum | FAP | response to calcium ion | 33/2622 | 149/18723 | 4.52e-03 | 3.08e-02 | 33 |
GO:00100384 | Colorectum | FAP | response to metal ion | 70/2622 | 373/18723 | 5.95e-03 | 3.75e-02 | 70 |
GO:00353061 | Colorectum | FAP | positive regulation of dephosphorylation | 16/2622 | 59/18723 | 5.95e-03 | 3.75e-02 | 16 |
GO:00423064 | Colorectum | FAP | regulation of protein import into nucleus | 16/2622 | 60/18723 | 7.08e-03 | 4.33e-02 | 16 |
GO:00423073 | Colorectum | FAP | positive regulation of protein import into nucleus | 12/2622 | 41/18723 | 8.57e-03 | 4.96e-02 | 12 |
GO:19038295 | Colorectum | CRC | positive regulation of cellular protein localization | 61/2078 | 276/18723 | 9.59e-08 | 1.17e-05 | 61 |
GO:00163114 | Colorectum | CRC | dephosphorylation | 79/2078 | 417/18723 | 1.27e-06 | 7.21e-05 | 79 |
GO:00512225 | Colorectum | CRC | positive regulation of protein transport | 61/2078 | 303/18723 | 2.73e-06 | 1.27e-04 | 61 |
GO:00323885 | Colorectum | CRC | positive regulation of intracellular transport | 45/2078 | 202/18723 | 3.54e-06 | 1.54e-04 | 45 |
GO:19049515 | Colorectum | CRC | positive regulation of establishment of protein localization | 62/2078 | 319/18723 | 7.44e-06 | 2.72e-04 | 62 |
GO:00903165 | Colorectum | CRC | positive regulation of intracellular protein transport | 37/2078 | 160/18723 | 1.04e-05 | 3.44e-04 | 37 |
GO:00468245 | Colorectum | CRC | positive regulation of nucleocytoplasmic transport | 19/2078 | 62/18723 | 2.57e-05 | 7.16e-04 | 19 |
GO:00069135 | Colorectum | CRC | nucleocytoplasmic transport | 57/2078 | 301/18723 | 3.71e-05 | 9.18e-04 | 57 |
GO:00511695 | Colorectum | CRC | nuclear transport | 57/2078 | 301/18723 | 3.71e-05 | 9.18e-04 | 57 |
GO:00725945 | Colorectum | CRC | establishment of protein localization to organelle | 74/2078 | 422/18723 | 4.38e-05 | 1.05e-03 | 74 |
GO:00353035 | Colorectum | CRC | regulation of dephosphorylation | 30/2078 | 128/18723 | 5.27e-05 | 1.20e-03 | 30 |
GO:00468225 | Colorectum | CRC | regulation of nucleocytoplasmic transport | 26/2078 | 106/18723 | 7.24e-05 | 1.53e-03 | 26 |
GO:00323865 | Colorectum | CRC | regulation of intracellular transport | 61/2078 | 337/18723 | 7.94e-05 | 1.65e-03 | 61 |
GO:00331575 | Colorectum | CRC | regulation of intracellular protein transport | 45/2078 | 229/18723 | 9.62e-05 | 1.95e-03 | 45 |
GO:00423065 | Colorectum | CRC | regulation of protein import into nucleus | 16/2078 | 60/18723 | 6.37e-04 | 8.46e-03 | 16 |
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 |
CHP2 | SNV | Missense_Mutation | rs138042112 | c.523N>A | p.Val175Met | p.V175M | O43745 | protein_coding | tolerated(0.08) | benign(0) | TCGA-A1-A0SG-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | | SD |
CHP2 | SNV | Missense_Mutation | novel | c.326N>C | p.Leu109Pro | p.L109P | O43745 | protein_coding | deleterious(0.04) | benign(0.071) | TCGA-AC-A62V-01 | Breast | breast invasive carcinoma | Male | <65 | III/IV | Targeted Molecular therapy | denosumab | PD |
CHP2 | SNV | Missense_Mutation | novel | c.462G>T | p.Glu154Asp | p.E154D | O43745 | protein_coding | tolerated(0.45) | benign(0) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CHP2 | SNV | Missense_Mutation | rs773423633 | c.475N>T | p.Arg159Cys | p.R159C | O43745 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-A6-6653-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD |
CHP2 | SNV | Missense_Mutation | | c.479N>T | p.Thr160Met | p.T160M | O43745 | protein_coding | deleterious(0) | probably_damaging(0.981) | TCGA-D5-6537-01 | Colorectum | colon adenocarcinoma | Male | <65 | III/IV | Unknown | Unknown | PD |
CHP2 | SNV | Missense_Mutation | novel | c.289G>T | p.Asp97Tyr | p.D97Y | O43745 | protein_coding | deleterious(0.05) | benign(0.003) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
CHP2 | SNV | Missense_Mutation | rs756892483 | c.512N>T | p.Ala171Val | p.A171V | O43745 | protein_coding | tolerated(0.28) | benign(0.027) | TCGA-AP-A056-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
CHP2 | SNV | Missense_Mutation | novel | c.344A>C | p.Lys115Thr | p.K115T | O43745 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AP-A1E0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | SD |
CHP2 | SNV | Missense_Mutation | rs368850634 | c.289N>A | p.Asp97Asn | p.D97N | O43745 | protein_coding | tolerated(0.32) | benign(0.013) | TCGA-AX-A06D-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Chemotherapy | carboplatin | PD |
CHP2 | SNV | Missense_Mutation | rs751008002 | c.578N>A | p.Arg193Gln | p.R193Q | O43745 | protein_coding | deleterious(0.02) | benign(0.34) | TCGA-AX-A2HC-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | paclitaxel | PD |