Tissue | Expression Dynamics | Abbreviation |
Colorectum (GSE201348) | | FAP: Familial adenomatous polyposis |
CRC: Colorectal cancer |
Colorectum (HTA11) | | AD: Adenomas |
SER: Sessile serrated lesions |
MSI-H: Microsatellite-high colorectal cancer |
MSS: Microsatellite stable colorectal cancer |
Esophagus | | ESCC: Esophageal squamous cell carcinoma |
HGIN: High-grade intraepithelial neoplasias |
LGIN: Low-grade intraepithelial neoplasias |
GC | | 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 |
Liver | | HCC: Hepatocellular carcinoma |
NAFLD: Non-alcoholic fatty liver disease |
Lung | | AAH: Atypical adenomatous hyperplasia |
AIS: Adenocarcinoma in situ |
IAC: Invasive lung adenocarcinoma |
MIA: Minimally invasive adenocarcinoma |
Oral Cavity | | EOLP: Erosive Oral lichen planus |
LP: leukoplakia |
NEOLP: Non-erosive oral lichen planus |
OSCC: Oral squamous cell carcinoma |
Prostate | | BPH: Benign Prostatic Hyperplasia |
Skin | | AK: Actinic keratosis |
cSCC: Cutaneous squamous cell carcinoma |
SCCIS:squamous cell carcinoma in situ |
Thyroid | | ATC: Anaplastic thyroid cancer |
HT: Hashimoto's thyroiditis |
PTC: Papillary thyroid cancer |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
GO:000975517 | Skin | AK | hormone-mediated signaling pathway | 34/1910 | 190/18723 | 8.18e-04 | 6.80e-03 | 34 |
GO:000918525 | Skin | AK | ribonucleoside diphosphate metabolic process | 22/1910 | 106/18723 | 9.13e-04 | 7.49e-03 | 22 |
GO:000913525 | Skin | AK | purine nucleoside diphosphate metabolic process | 21/1910 | 103/18723 | 1.50e-03 | 1.08e-02 | 21 |
GO:000917925 | Skin | AK | purine ribonucleoside diphosphate metabolic process | 21/1910 | 103/18723 | 1.50e-03 | 1.08e-02 | 21 |
GO:00607665 | Skin | AK | negative regulation of androgen receptor signaling pathway | 6/1910 | 15/18723 | 2.48e-03 | 1.61e-02 | 6 |
GO:004340920 | Skin | AK | negative regulation of MAPK cascade | 31/1910 | 180/18723 | 2.53e-03 | 1.63e-02 | 31 |
GO:19037983 | Skin | AK | regulation of production of miRNAs involved in gene silencing by miRNA | 8/1910 | 25/18723 | 2.55e-03 | 1.64e-02 | 8 |
GO:004232625 | Skin | AK | negative regulation of phosphorylation | 57/1910 | 385/18723 | 2.61e-03 | 1.68e-02 | 57 |
GO:000913220 | Skin | AK | nucleoside diphosphate metabolic process | 23/1910 | 124/18723 | 3.35e-03 | 2.05e-02 | 23 |
GO:00709202 | Skin | AK | regulation of production of small RNA involved in gene silencing by RNA | 8/1910 | 26/18723 | 3.36e-03 | 2.05e-02 | 8 |
GO:000609126 | Skin | AK | generation of precursor metabolites and energy | 69/1910 | 490/18723 | 3.59e-03 | 2.16e-02 | 69 |
GO:00463295 | Skin | AK | negative regulation of JNK cascade | 10/1910 | 38/18723 | 3.89e-03 | 2.29e-02 | 10 |
GO:190357820 | Skin | AK | regulation of ATP metabolic process | 17/1910 | 87/18723 | 6.32e-03 | 3.38e-02 | 17 |
GO:0006091111 | Skin | cSCC | generation of precursor metabolites and energy | 224/4864 | 490/18723 | 1.13e-21 | 2.21e-19 | 224 |
GO:0046034112 | Skin | cSCC | ATP metabolic process | 142/4864 | 277/18723 | 1.38e-19 | 1.96e-17 | 142 |
GO:000705115 | Skin | cSCC | spindle organization | 96/4864 | 184/18723 | 2.59e-14 | 1.77e-12 | 96 |
GO:000989527 | Skin | cSCC | negative regulation of catabolic process | 133/4864 | 320/18723 | 6.99e-10 | 2.77e-08 | 133 |
GO:005122513 | Skin | cSCC | spindle assembly | 60/4864 | 117/18723 | 4.15e-09 | 1.41e-07 | 60 |
GO:004854529 | Skin | cSCC | response to steroid hormone | 135/4864 | 339/18723 | 1.34e-08 | 4.09e-07 | 135 |
GO:003052227 | Skin | cSCC | intracellular receptor signaling pathway | 108/4864 | 265/18723 | 9.21e-08 | 2.21e-06 | 108 |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa04919 | Colorectum | AD | Thyroid hormone signaling pathway | 51/2092 | 121/8465 | 1.71e-05 | 1.73e-04 | 1.10e-04 | 51 |
hsa049191 | Colorectum | AD | Thyroid hormone signaling pathway | 51/2092 | 121/8465 | 1.71e-05 | 1.73e-04 | 1.10e-04 | 51 |
hsa049192 | Colorectum | SER | Thyroid hormone signaling pathway | 40/1580 | 121/8465 | 1.02e-04 | 1.06e-03 | 7.67e-04 | 40 |
hsa04350 | Colorectum | SER | TGF-beta signaling pathway | 31/1580 | 108/8465 | 7.00e-03 | 3.77e-02 | 2.74e-02 | 31 |
hsa049193 | Colorectum | SER | Thyroid hormone signaling pathway | 40/1580 | 121/8465 | 1.02e-04 | 1.06e-03 | 7.67e-04 | 40 |
hsa043501 | Colorectum | SER | TGF-beta signaling pathway | 31/1580 | 108/8465 | 7.00e-03 | 3.77e-02 | 2.74e-02 | 31 |
hsa049194 | Colorectum | MSS | Thyroid hormone signaling pathway | 46/1875 | 121/8465 | 5.04e-05 | 4.97e-04 | 3.05e-04 | 46 |
hsa049195 | Colorectum | MSS | Thyroid hormone signaling pathway | 46/1875 | 121/8465 | 5.04e-05 | 4.97e-04 | 3.05e-04 | 46 |
hsa049196 | Colorectum | MSI-H | Thyroid hormone signaling pathway | 21/797 | 121/8465 | 4.18e-03 | 4.10e-02 | 3.44e-02 | 21 |
hsa049197 | Colorectum | MSI-H | Thyroid hormone signaling pathway | 21/797 | 121/8465 | 4.18e-03 | 4.10e-02 | 3.44e-02 | 21 |
hsa049198 | Colorectum | FAP | Thyroid hormone signaling pathway | 41/1404 | 121/8465 | 2.28e-06 | 4.28e-05 | 2.60e-05 | 41 |
hsa05202 | Colorectum | FAP | Transcriptional misregulation in cancer | 45/1404 | 193/8465 | 9.19e-03 | 3.33e-02 | 2.03e-02 | 45 |
hsa049199 | Colorectum | FAP | Thyroid hormone signaling pathway | 41/1404 | 121/8465 | 2.28e-06 | 4.28e-05 | 2.60e-05 | 41 |
hsa052021 | Colorectum | FAP | Transcriptional misregulation in cancer | 45/1404 | 193/8465 | 9.19e-03 | 3.33e-02 | 2.03e-02 | 45 |
hsa0491910 | Colorectum | CRC | Thyroid hormone signaling pathway | 35/1091 | 121/8465 | 2.05e-06 | 6.85e-05 | 4.64e-05 | 35 |
hsa0491911 | Colorectum | CRC | Thyroid hormone signaling pathway | 35/1091 | 121/8465 | 2.05e-06 | 6.85e-05 | 4.64e-05 | 35 |
hsa0491928 | Esophagus | ESCC | Thyroid hormone signaling pathway | 78/4205 | 121/8465 | 6.79e-04 | 2.23e-03 | 1.14e-03 | 78 |
hsa043507 | Esophagus | ESCC | TGF-beta signaling pathway | 69/4205 | 108/8465 | 1.92e-03 | 5.54e-03 | 2.84e-03 | 69 |
hsa052028 | Esophagus | ESCC | Transcriptional misregulation in cancer | 116/4205 | 193/8465 | 2.08e-03 | 5.95e-03 | 3.05e-03 | 116 |
hsa015227 | Esophagus | ESCC | Endocrine resistance | 63/4205 | 98/8465 | 2.38e-03 | 6.58e-03 | 3.37e-03 | 63 |
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 |
NCOR1 | SNV | Missense_Mutation | novel | c.19C>T | p.Pro7Ser | p.P7S | O75376 | protein_coding | deleterious(0) | possibly_damaging(0.621) | TCGA-3C-AALK-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | docetaxel | SD |
NCOR1 | SNV | Missense_Mutation | | c.1591N>C | p.Glu531Gln | p.E531Q | O75376 | protein_coding | tolerated(0.07) | benign(0.042) | TCGA-A1-A0SN-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | ac | SD |
NCOR1 | SNV | Missense_Mutation | | c.3488N>A | p.Gly1163Asp | p.G1163D | O75376 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-A2-A0CU-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | tamoxiphen | SD |
NCOR1 | SNV | Missense_Mutation | | c.7010N>T | p.Ser2337Phe | p.S2337F | O75376 | protein_coding | deleterious(0) | probably_damaging(0.991) | TCGA-A8-A08R-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
NCOR1 | SNV | Missense_Mutation | novel | c.2161G>A | p.Glu721Lys | p.E721K | O75376 | protein_coding | deleterious(0.02) | probably_damaging(0.971) | TCGA-AC-A8OP-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NCOR1 | SNV | Missense_Mutation | rs367758096 | c.451N>A | p.Gly151Ser | p.G151S | O75376 | protein_coding | tolerated(0.18) | benign(0.001) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NCOR1 | SNV | Missense_Mutation | | c.5725N>T | p.Pro1909Ser | p.P1909S | O75376 | protein_coding | tolerated(0.09) | benign(0.162) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NCOR1 | SNV | Missense_Mutation | | c.5263N>T | p.Arg1755Cys | p.R1755C | O75376 | protein_coding | deleterious(0) | probably_damaging(0.925) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
NCOR1 | SNV | Missense_Mutation | rs754505756 | c.4882N>T | p.Arg1628Cys | p.R1628C | O75376 | protein_coding | deleterious(0) | probably_damaging(0.99) | TCGA-AO-A128-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD |
NCOR1 | SNV | Missense_Mutation | | c.3644N>G | p.Lys1215Arg | p.K1215R | O75376 | protein_coding | deleterious(0.03) | probably_damaging(0.985) | TCGA-AR-A0TV-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |