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Gene: IGFN1 |
Gene summary for IGFN1 |
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Gene information | Species | Human | Gene symbol | IGFN1 | Gene ID | 91156 |
Gene name | immunoglobulin like and fibronectin type III domain containing 1 | |
Gene Alias | EEF1A2BP1 | |
Cytomap | 1q32.1 | |
Gene Type | protein-coding | GO ID | GO:0001654 | UniProtAcc | Q86VF2 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
91156 | IGFN1 | PTC01 | Human | Thyroid | PTC | 7.13e-05 | 6.12e-02 | 0.1899 |
91156 | IGFN1 | PTC05 | Human | Thyroid | PTC | 8.79e-33 | 2.36e+00 | 0.2065 |
91156 | IGFN1 | PTC06 | Human | Thyroid | PTC | 1.43e-21 | 1.11e+00 | 0.2057 |
91156 | IGFN1 | ATC09 | Human | Thyroid | ATC | 4.63e-07 | 3.39e-01 | 0.2871 |
91156 | IGFN1 | ATC1 | Human | Thyroid | ATC | 3.84e-05 | 3.42e-01 | 0.2878 |
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Tissue | Expression Dynamics | Abbreviation |
Thyroid | ![]() | ATC: Anaplastic thyroid cancer |
HT: Hashimoto's thyroiditis | ||
PTC: Papillary thyroid cancer |
∗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:0034329111 | Thyroid | PTC | cell junction assembly | 180/5968 | 420/18723 | 1.17e-06 | 1.69e-05 | 180 |
GO:00508089 | Thyroid | PTC | synapse organization | 161/5968 | 426/18723 | 5.11e-03 | 2.36e-02 | 161 |
GO:003432924 | Thyroid | ATC | cell junction assembly | 187/6293 | 420/18723 | 1.71e-06 | 2.08e-05 | 187 |
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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 |
IGFN1 | SNV | Missense_Mutation | novel | c.4408N>T | p.Met1470Leu | p.M1470L | Q86VF2 | protein_coding | tolerated_low_confidence(0.49) | benign(0.019) | TCGA-A1-A0SO-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | SD | |
IGFN1 | SNV | Missense_Mutation | c.9032N>A | p.Leu3011Gln | p.L3011Q | Q86VF2 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-A1-A0SO-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | SD | ||
IGFN1 | SNV | Missense_Mutation | rs757869019 | c.3595G>A | p.Ala1199Thr | p.A1199T | Q86VF2 | protein_coding | tolerated(0.12) | possibly_damaging(0.691) | TCGA-A2-A0CK-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | taxotere | CR |
IGFN1 | SNV | Missense_Mutation | novel | c.2332N>T | p.Pro778Ser | p.P778S | Q86VF2 | protein_coding | tolerated(0.11) | unknown(0) | TCGA-A7-A4SD-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | taxotere | CR |
IGFN1 | SNV | Missense_Mutation | c.10990G>A | p.Asp3664Asn | p.D3664N | Q86VF2 | protein_coding | tolerated(0.35) | benign(0.375) | TCGA-A7-A56D-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Hormone Therapy | arimidex | SD | |
IGFN1 | SNV | Missense_Mutation | novel | c.5225N>G | p.Asn1742Ser | p.N1742S | Q86VF2 | protein_coding | tolerated_low_confidence(0.12) | unknown(0) | TCGA-A7-A6VX-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Chemotherapy | docetaxel | CR |
IGFN1 | SNV | Missense_Mutation | novel | c.8372C>A | p.Pro2791His | p.P2791H | Q86VF2 | protein_coding | deleterious(0.04) | benign(0.003) | TCGA-AN-A046-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
IGFN1 | SNV | Missense_Mutation | c.7643G>T | p.Gly2548Val | p.G2548V | Q86VF2 | protein_coding | deleterious(0) | probably_damaging(0.988) | TCGA-AN-A04D-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Unknown | Unknown | SD | |
IGFN1 | SNV | Missense_Mutation | rs577651874 | c.440N>A | p.Arg147Gln | p.R147Q | Q86VF2 | protein_coding | deleterious(0) | unknown(0) | TCGA-AO-A128-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | SD |
IGFN1 | SNV | Missense_Mutation | c.9358N>A | p.Leu3120Ile | p.L3120I | Q86VF2 | protein_coding | tolerated(0.14) | possibly_damaging(0.672) | TCGA-AO-A128-01 | Breast | breast invasive carcinoma | Female | <65 | I/II | Chemotherapy | doxorubicin | 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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