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Gene: MYEOV |
Gene summary for MYEOV |
Gene summary. |
Gene information | Species | Human | Gene symbol | MYEOV | Gene ID | 26579 |
Gene name | myeloma overexpressed | |
Gene Alias | OCIM | |
Cytomap | 11q13.3 | |
Gene Type | protein-coding | GO ID | GO:0003674 | UniProtAcc | A0A024R5F1 |
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Malignant transformation analysis |
Identification of the aberrant gene expression in precancerous and cancerous lesions by comparing the gene expression of stem-like cells in diseased tissues with normal stem cells |
Malignant transformation involving gene list. |
Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
26579 | MYEOV | LZE8T | Human | Esophagus | ESCC | 1.06e-18 | 1.29e+00 | 0.067 |
26579 | MYEOV | LZE20T | Human | Esophagus | ESCC | 1.97e-04 | 3.80e-01 | 0.0662 |
26579 | MYEOV | LZE24T | Human | Esophagus | ESCC | 1.09e-06 | 3.91e-01 | 0.0596 |
26579 | MYEOV | LZE21T | Human | Esophagus | ESCC | 6.52e-03 | 4.49e-01 | 0.0655 |
26579 | MYEOV | P1T-E | Human | Esophagus | ESCC | 1.05e-09 | 1.12e+00 | 0.0875 |
26579 | MYEOV | P5T-E | Human | Esophagus | ESCC | 3.50e-02 | 9.36e-02 | 0.1327 |
26579 | MYEOV | P8T-E | Human | Esophagus | ESCC | 6.56e-15 | 4.66e-01 | 0.0889 |
26579 | MYEOV | P10T-E | Human | Esophagus | ESCC | 8.28e-115 | 1.71e+00 | 0.116 |
26579 | MYEOV | P17T-E | Human | Esophagus | ESCC | 2.60e-06 | 4.29e-01 | 0.1278 |
26579 | MYEOV | P23T-E | Human | Esophagus | ESCC | 2.27e-24 | 2.06e+00 | 0.108 |
26579 | MYEOV | P24T-E | Human | Esophagus | ESCC | 4.44e-08 | 2.48e-01 | 0.1287 |
26579 | MYEOV | P32T-E | Human | Esophagus | ESCC | 4.40e-09 | 3.48e-01 | 0.1666 |
26579 | MYEOV | P36T-E | Human | Esophagus | ESCC | 3.61e-22 | 1.37e+00 | 0.1187 |
26579 | MYEOV | P37T-E | Human | Esophagus | ESCC | 1.84e-22 | 5.14e-01 | 0.1371 |
26579 | MYEOV | P38T-E | Human | Esophagus | ESCC | 4.17e-18 | 5.68e-01 | 0.127 |
26579 | MYEOV | P39T-E | Human | Esophagus | ESCC | 4.41e-07 | 4.04e-01 | 0.0894 |
26579 | MYEOV | P47T-E | Human | Esophagus | ESCC | 3.50e-02 | 1.90e-01 | 0.1067 |
26579 | MYEOV | P52T-E | Human | Esophagus | ESCC | 2.08e-40 | 1.07e+00 | 0.1555 |
26579 | MYEOV | P54T-E | Human | Esophagus | ESCC | 1.34e-09 | 5.05e-01 | 0.0975 |
26579 | MYEOV | P56T-E | Human | Esophagus | ESCC | 3.37e-32 | 2.81e+00 | 0.1613 |
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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. |
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Malignant transformation related pathway analysis |
Find out the enriched GO biological processes and KEGG pathways involved in transition from healthy to precancer to cancer |
Figure of enriched GO biological processes. |
Tissue | Disease Stage | Enriched GO biological Processes |
Thyroid | PTC | |
Thyroid | goiters | |
Thyroid | ATC |
∗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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Enriched GO biological processes. |
GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
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Enriched KEGG pathways. |
Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
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Cell-cell communication analysis |
Identification of potential cell-cell interactions between two cell types and their ligand-receptor pairs for different disease states |
Ligand | Receptor | LRpair | Pathway | Tissue | Disease Stage |
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Single-cell gene regulatory network inference analysis |
Find out the significant the regulons (TFs) and the target genes of each regulon across cell types for different disease states |
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 |
Annotation of somatic variants for genes involved in malignant transformation |
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 |
MYEOV | SNV | Missense_Mutation | c.490C>T | p.His164Tyr | p.H164Y | Q96EZ4 | protein_coding | tolerated_low_confidence(0.35) | benign(0.029) | TCGA-AC-A23H-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | PD | |
MYEOV | SNV | Missense_Mutation | novel | c.454N>A | p.Ser152Thr | p.S152T | Q96EZ4 | protein_coding | deleterious_low_confidence(0) | possibly_damaging(0.583) | TCGA-AC-A2BK-01 | Breast | breast invasive carcinoma | Female | >=65 | III/IV | Chemotherapy | cytoxan | CR |
MYEOV | SNV | Missense_Mutation | novel | c.904C>A | p.Leu302Ile | p.L302I | Q96EZ4 | protein_coding | benign(0.011) | TCGA-AA-3811-01 | Colorectum | colon adenocarcinoma | Female | >=65 | III/IV | Unknown | Unknown | PD | |
MYEOV | SNV | Missense_Mutation | c.487N>A | p.Ala163Thr | p.A163T | Q96EZ4 | protein_coding | deleterious_low_confidence(0.02) | benign(0.06) | TCGA-AD-6889-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Chemotherapy | xeloda | PD | |
MYEOV | SNV | Missense_Mutation | c.577G>A | p.Glu193Lys | p.E193K | Q96EZ4 | protein_coding | deleterious_low_confidence(0) | possibly_damaging(0.896) | TCGA-EI-6507-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |
MYEOV | SNV | Missense_Mutation | novel | c.802G>T | p.Ala268Ser | p.A268S | Q96EZ4 | protein_coding | deleterious_low_confidence(0) | benign(0.266) | TCGA-A5-A0G1-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MYEOV | SNV | Missense_Mutation | novel | c.578N>T | p.Glu193Val | p.E193V | Q96EZ4 | protein_coding | deleterious_low_confidence(0) | probably_damaging(0.979) | TCGA-A5-A2K5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MYEOV | SNV | Missense_Mutation | rs754058415 | c.484N>A | p.Val162Ile | p.V162I | Q96EZ4 | protein_coding | tolerated_low_confidence(1) | benign(0) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
MYEOV | SNV | Missense_Mutation | rs543791821 | c.611G>A | p.Arg204His | p.R204H | Q96EZ4 | protein_coding | tolerated_low_confidence(0.21) | benign(0) | TCGA-D1-A103-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
MYEOV | SNV | Missense_Mutation | novel | c.623G>A | p.Arg208Gln | p.R208Q | Q96EZ4 | protein_coding | tolerated_low_confidence(0.25) | benign(0.031) | TCGA-FI-A2D0-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
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Related drugs of malignant transformation related genes |
Identification of chemicals and drugs interact with genes involved in malignant transfromation |
(DGIdb 4.0) |
Entrez ID | Symbol | Category | Interaction Types | Drug Claim Name | Drug Name | PMIDs |
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