Tissue | Expression Dynamics | Abbreviation |
Cervix | | CC: Cervix cancer |
HSIL_HPV: HPV-infected high-grade squamous intraepithelial lesions |
N_HPV: HPV-infected normal cervix |
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 |
Endometrium | | AEH: Atypical endometrial hyperplasia |
EEC: Endometrioid Cancer |
Esophagus | | ESCC: Esophageal squamous cell carcinoma |
HGIN: High-grade intraepithelial neoplasias |
LGIN: Low-grade intraepithelial neoplasias |
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:002260410 | Cervix | CC | regulation of cell morphogenesis | 84/2311 | 309/18723 | 1.00e-12 | 4.29e-10 | 84 |
GO:00083608 | Cervix | CC | regulation of cell shape | 38/2311 | 154/18723 | 1.86e-05 | 3.46e-04 | 38 |
GO:00308657 | Cervix | CC | cortical cytoskeleton organization | 19/2311 | 61/18723 | 8.72e-05 | 1.16e-03 | 19 |
GO:00308667 | Cervix | CC | cortical actin cytoskeleton organization | 12/2311 | 40/18723 | 2.44e-03 | 1.71e-02 | 12 |
GO:0022604 | Colorectum | AD | regulation of cell morphogenesis | 109/3918 | 309/18723 | 3.08e-09 | 2.07e-07 | 109 |
GO:0008360 | Colorectum | AD | regulation of cell shape | 56/3918 | 154/18723 | 7.01e-06 | 1.73e-04 | 56 |
GO:0030866 | Colorectum | AD | cortical actin cytoskeleton organization | 19/3918 | 40/18723 | 1.58e-04 | 2.20e-03 | 19 |
GO:0030865 | Colorectum | AD | cortical cytoskeleton organization | 25/3918 | 61/18723 | 2.96e-04 | 3.60e-03 | 25 |
GO:00226041 | Colorectum | SER | regulation of cell morphogenesis | 89/2897 | 309/18723 | 1.51e-09 | 1.52e-07 | 89 |
GO:00083601 | Colorectum | SER | regulation of cell shape | 43/2897 | 154/18723 | 5.47e-05 | 1.30e-03 | 43 |
GO:00308651 | Colorectum | SER | cortical cytoskeleton organization | 19/2897 | 61/18723 | 1.59e-03 | 1.69e-02 | 19 |
GO:00308661 | Colorectum | SER | cortical actin cytoskeleton organization | 14/2897 | 40/18723 | 1.88e-03 | 1.90e-02 | 14 |
GO:00226042 | Colorectum | MSS | regulation of cell morphogenesis | 103/3467 | 309/18723 | 2.70e-10 | 2.56e-08 | 103 |
GO:00083602 | Colorectum | MSS | regulation of cell shape | 52/3467 | 154/18723 | 4.40e-06 | 1.24e-04 | 52 |
GO:00308652 | Colorectum | MSS | cortical cytoskeleton organization | 24/3467 | 61/18723 | 1.16e-04 | 1.81e-03 | 24 |
GO:00308662 | Colorectum | MSS | cortical actin cytoskeleton organization | 17/3467 | 40/18723 | 3.87e-04 | 4.86e-03 | 17 |
GO:00226044 | Colorectum | FAP | regulation of cell morphogenesis | 87/2622 | 309/18723 | 4.89e-11 | 1.87e-08 | 87 |
GO:00083603 | Colorectum | FAP | regulation of cell shape | 43/2622 | 154/18723 | 4.55e-06 | 1.52e-04 | 43 |
GO:00308663 | Colorectum | FAP | cortical actin cytoskeleton organization | 14/2622 | 40/18723 | 6.94e-04 | 7.50e-03 | 14 |
GO:00308653 | Colorectum | FAP | cortical cytoskeleton organization | 18/2622 | 61/18723 | 1.30e-03 | 1.20e-02 | 18 |
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 |
FMNL2 | SNV | Missense_Mutation | | c.2992N>T | p.Leu998Phe | p.L998F | Q96PY5 | protein_coding | tolerated(0.13) | possibly_damaging(0.749) | TCGA-A7-A26H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | anastrozole | PD |
FMNL2 | SNV | Missense_Mutation | novel | c.1088N>C | p.Lys363Thr | p.K363T | Q96PY5 | protein_coding | deleterious(0.01) | probably_damaging(0.994) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FMNL2 | SNV | Missense_Mutation | novel | c.1355N>T | p.Arg452Ile | p.R452I | Q96PY5 | protein_coding | deleterious(0) | probably_damaging(0.994) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FMNL2 | SNV | Missense_Mutation | novel | c.3053N>T | p.Ser1018Phe | p.S1018F | Q96PY5 | protein_coding | deleterious(0.02) | benign(0.159) | TCGA-BH-A1FC-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FMNL2 | SNV | Missense_Mutation | rs377550607 | c.571N>T | p.Arg191Cys | p.R191C | Q96PY5 | protein_coding | deleterious(0.01) | probably_damaging(0.992) | TCGA-E9-A1R6-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD |
FMNL2 | SNV | Missense_Mutation | | c.733N>G | p.Pro245Ala | p.P245A | Q96PY5 | protein_coding | tolerated(0.08) | benign(0.187) | TCGA-E9-A243-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | PD |
FMNL2 | SNV | Missense_Mutation | | c.2839G>A | p.Ala947Thr | p.A947T | Q96PY5 | protein_coding | deleterious(0) | probably_damaging(0.963) | TCGA-2W-A8YY-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
FMNL2 | SNV | Missense_Mutation | novel | c.1002G>A | p.Met334Ile | p.M334I | Q96PY5 | protein_coding | deleterious(0) | probably_damaging(0.946) | TCGA-HM-A4S6-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | cisplatin | CR |
FMNL2 | SNV | Missense_Mutation | novel | c.2956N>A | p.Glu986Lys | p.E986K | Q96PY5 | protein_coding | tolerated(0.23) | benign(0.159) | TCGA-VS-A8EL-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Chemotherapy | cisplatin | CR |
FMNL2 | SNV | Missense_Mutation | novel | c.1150N>A | p.Asp384Asn | p.D384N | Q96PY5 | protein_coding | deleterious(0) | probably_damaging(0.993) | TCGA-ZJ-AAXU-01 | Cervix | cervical & endocervical cancer | Female | <65 | I/II | Unknown | Unknown | SD |