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Gene: FREM2 |
Gene summary for FREM2 |
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Gene information | Species | Human | Gene symbol | FREM2 | Gene ID | 341640 |
Gene name | FRAS1 related extracellular matrix 2 | |
Gene Alias | CRYPTOP | |
Cytomap | 13q13.3 | |
Gene Type | protein-coding | GO ID | GO:0001654 | UniProtAcc | Q5SZK8 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
341640 | FREM2 | RNA-P25T1-P25T1-1 | Human | Lung | AIS | 6.77e-08 | 5.13e-01 | -0.2116 |
341640 | FREM2 | RNA-P25T1-P25T1-2 | Human | Lung | AIS | 7.32e-03 | 5.61e-01 | -0.1941 |
341640 | FREM2 | RNA-P25T1-P25T1-4 | Human | Lung | AIS | 6.02e-04 | 4.99e-01 | -0.2119 |
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Tissue | Expression Dynamics | Abbreviation |
Lung | ![]() | AAH: Atypical adenomatous hyperplasia |
AIS: Adenocarcinoma in situ | ||
IAC: Invasive lung adenocarcinoma | ||
MIA: Minimally invasive adenocarcinoma |
∗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 |
GO:000165511 | Lung | AIS | urogenital system development | 63/1849 | 338/18723 | 5.46e-07 | 4.08e-05 | 63 |
GO:000182211 | Lung | AIS | kidney development | 53/1849 | 293/18723 | 1.04e-05 | 4.25e-04 | 53 |
GO:007200111 | Lung | AIS | renal system development | 54/1849 | 302/18723 | 1.21e-05 | 4.71e-04 | 54 |
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Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
hsa045122 | Lung | AIS | ECM-receptor interaction | 20/961 | 89/8465 | 1.95e-03 | 1.26e-02 | 8.09e-03 | 20 |
hsa045123 | Lung | AIS | ECM-receptor interaction | 20/961 | 89/8465 | 1.95e-03 | 1.26e-02 | 8.09e-03 | 20 |
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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 |
FREM2 | SNV | Missense_Mutation | novel | c.6848N>T | p.Ser2283Leu | p.S2283L | Q5SZK8 | protein_coding | deleterious(0) | probably_damaging(0.962) | TCGA-A2-A25A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Cytoxan | SD |
FREM2 | SNV | Missense_Mutation | rs149553690 | c.9245N>A | p.Arg3082His | p.R3082H | Q5SZK8 | protein_coding | tolerated(0.12) | benign(0.019) | TCGA-A2-A25A-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unspecific | Cytoxan | SD |
FREM2 | SNV | Missense_Mutation | rs532760237 | c.6012A>C | p.Lys2004Asn | p.K2004N | Q5SZK8 | protein_coding | tolerated(0.52) | benign(0.185) | TCGA-A8-A07W-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Hormone Therapy | exemestane | SD |
FREM2 | SNV | Missense_Mutation | rs374734549 | c.6718N>G | p.Ile2240Val | p.I2240V | Q5SZK8 | protein_coding | tolerated(0.75) | benign(0.182) | TCGA-A8-A093-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Hormone Therapy | tamoxiphen | SD |
FREM2 | SNV | Missense_Mutation | rs192388331 | c.3872N>T | p.Thr1291Met | p.T1291M | Q5SZK8 | protein_coding | tolerated(0.16) | benign(0.031) | TCGA-A8-A0AB-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | 5-fluorouracil | CR |
FREM2 | SNV | Missense_Mutation | c.6733N>A | p.Asp2245Asn | p.D2245N | Q5SZK8 | protein_coding | tolerated(0.19) | benign(0.005) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
FREM2 | SNV | Missense_Mutation | c.8731N>C | p.Tyr2911His | p.Y2911H | Q5SZK8 | protein_coding | tolerated(0.53) | benign(0.005) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
FREM2 | SNV | Missense_Mutation | novel | c.5459N>C | p.Gly1820Ala | p.G1820A | Q5SZK8 | protein_coding | deleterious(0.02) | benign(0.236) | TCGA-AC-A2BK-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | cytoxan | CR |
FREM2 | SNV | Missense_Mutation | novel | c.9089N>T | p.Arg3030Ile | p.R3030I | Q5SZK8 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
FREM2 | SNV | Missense_Mutation | c.3833T>C | p.Val1278Ala | p.V1278A | Q5SZK8 | protein_coding | tolerated(0.18) | benign(0.001) | TCGA-AN-A0AK-01 | Breast | breast invasive carcinoma | Female | >=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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