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Gene: APOM |
Gene summary for APOM |
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Gene information | Species | Human | Gene symbol | APOM | Gene ID | 55937 |
Gene name | apolipoprotein M | |
Gene Alias | G3a | |
Cytomap | 6p21.33 | |
Gene Type | protein-coding | GO ID | GO:0006807 | UniProtAcc | A0A1U9X793 |
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Malignant transformation analysis |
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Entrez ID | Symbol | Replicates | Species | Organ | Tissue | Adj P-value | Log2FC | Malignancy |
55937 | APOM | HCC1_Meng | Human | Liver | HCC | 1.24e-119 | 1.64e+00 | 0.0246 |
55937 | APOM | HCC2_Meng | Human | Liver | HCC | 1.67e-03 | -1.08e-01 | 0.0107 |
55937 | APOM | cirrhotic2 | Human | Liver | Cirrhotic | 8.53e-03 | 6.49e-03 | 0.0201 |
55937 | APOM | HCC1 | Human | Liver | HCC | 3.99e-13 | 3.49e+00 | 0.5336 |
55937 | APOM | HCC2 | Human | Liver | HCC | 9.69e-24 | 3.48e+00 | 0.5341 |
55937 | APOM | Pt13.a | Human | Liver | HCC | 6.49e-50 | 8.36e-01 | 0.021 |
55937 | APOM | Pt13.b | Human | Liver | HCC | 9.14e-56 | 5.76e-01 | 0.0251 |
55937 | APOM | Pt13.c | Human | Liver | HCC | 3.48e-02 | 4.74e-01 | 0.0076 |
55937 | APOM | Pt14.a | Human | Liver | HCC | 7.16e-03 | 1.48e-01 | 0.0169 |
55937 | APOM | Pt14.b | Human | Liver | HCC | 1.02e-05 | 3.59e-01 | 0.018 |
55937 | APOM | Pt14.d | Human | Liver | HCC | 3.31e-04 | 1.58e-01 | 0.0143 |
55937 | APOM | S014 | Human | Liver | HCC | 1.20e-26 | 2.27e+00 | 0.2254 |
55937 | APOM | S015 | Human | Liver | HCC | 4.49e-44 | 3.39e+00 | 0.2375 |
55937 | APOM | S016 | Human | Liver | HCC | 3.52e-26 | 2.73e+00 | 0.2243 |
55937 | APOM | S028 | Human | Liver | HCC | 3.95e-22 | 1.22e+00 | 0.2503 |
55937 | APOM | S029 | Human | Liver | HCC | 7.12e-24 | 1.65e+00 | 0.2581 |
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Tissue | Expression Dynamics | Abbreviation |
Liver | ![]() | HCC: Hepatocellular carcinoma |
NAFLD: Non-alcoholic fatty liver disease |
∗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:000686921 | Liver | HCC | lipid transport | 198/7958 | 398/18723 | 1.92e-03 | 9.78e-03 | 198 |
GO:00303012 | Liver | HCC | cholesterol transport | 65/7958 | 117/18723 | 2.95e-03 | 1.38e-02 | 65 |
GO:00159182 | Liver | HCC | sterol transport | 71/7958 | 130/18723 | 3.49e-03 | 1.58e-02 | 71 |
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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 |
APOM | insertion | In_Frame_Ins | novel | c.411_412insACGAGGTTGAGGCAGGAGAAT | p.Thr137_Gly138insThrArgLeuArgGlnGluAsn | p.T137_G138insTRLRQEN | O95445 | protein_coding | TCGA-AN-A03X-01 | Breast | breast invasive carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD | ||
APOM | SNV | Missense_Mutation | rs548136627 | c.100N>A | p.Val34Met | p.V34M | O95445 | protein_coding | tolerated(0.23) | benign(0.003) | TCGA-WS-AB45-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
APOM | SNV | Missense_Mutation | novel | c.563N>G | p.Asn188Ser | p.N188S | O95445 | protein_coding | tolerated_low_confidence(0.67) | benign(0) | TCGA-AG-A002-01 | Colorectum | rectum adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD |
APOM | SNV | Missense_Mutation | novel | c.274N>T | p.Asp92Tyr | p.D92Y | O95445 | protein_coding | deleterious(0) | possibly_damaging(0.487) | TCGA-A5-A0G2-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Unknown | Unknown | SD |
APOM | SNV | Missense_Mutation | rs753977558 | c.427C>T | p.Arg143Cys | p.R143C | O95445 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-AP-A1DV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
APOM | SNV | Missense_Mutation | novel | c.203N>G | p.Asn68Ser | p.N68S | O95445 | protein_coding | tolerated(0.14) | probably_damaging(0.99) | TCGA-AX-A2HD-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | III/IV | Unknown | Unknown | SD |
APOM | SNV | Missense_Mutation | rs529627933 | c.253C>T | p.Arg85Cys | p.R85C | O95445 | protein_coding | deleterious(0.01) | possibly_damaging(0.731) | TCGA-B5-A3FA-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | >=65 | I/II | Unknown | Unknown | SD |
APOM | SNV | Missense_Mutation | novel | c.445N>T | p.Arg149Cys | p.R149C | O95445 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-EO-A3AV-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatin | CR |
APOM | SNV | Missense_Mutation | novel | c.179T>C | p.Leu60Ser | p.L60S | O95445 | protein_coding | deleterious(0) | probably_damaging(1) | TCGA-FI-A2D5-01 | Endometrium | uterine corpus endometrioid carcinoma | Female | <65 | III/IV | Chemotherapy | carboplatinum | PD |
APOM | SNV | Missense_Mutation | c.83A>C | p.Gln28Pro | p.Q28P | O95445 | protein_coding | tolerated(0.43) | benign(0) | TCGA-DD-A119-01 | Liver | liver hepatocellular carcinoma | Male | <65 | III/IV | 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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