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Gene: MBOAT1 |
Gene summary for MBOAT1 |
 Gene summary. |
| Gene information | Species | Human | Gene symbol | MBOAT1 | Gene ID | 154141 |
| Gene name | membrane bound O-acyltransferase domain containing 1 | |
| Gene Alias | LPEAT1 | |
| Cytomap | 6p22.3 | |
| Gene Type | protein-coding | GO ID | GO:0006575 | UniProtAcc | Q6ZNC8 |
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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 |
| 154141 | MBOAT1 | P9T-E | Human | Esophagus | ESCC | 5.23e-05 | 1.46e-01 | 0.1131 |
| 154141 | MBOAT1 | P10T-E | Human | Esophagus | ESCC | 6.20e-05 | 1.03e-01 | 0.116 |
| 154141 | MBOAT1 | P11T-E | Human | Esophagus | ESCC | 2.46e-02 | 1.44e-01 | 0.1426 |
| 154141 | MBOAT1 | P12T-E | Human | Esophagus | ESCC | 5.27e-09 | 1.51e-01 | 0.1122 |
| 154141 | MBOAT1 | P15T-E | Human | Esophagus | ESCC | 2.11e-03 | 1.08e-01 | 0.1149 |
| 154141 | MBOAT1 | P20T-E | Human | Esophagus | ESCC | 2.18e-03 | 1.05e-01 | 0.1124 |
| 154141 | MBOAT1 | P21T-E | Human | Esophagus | ESCC | 8.17e-07 | 1.34e-01 | 0.1617 |
| 154141 | MBOAT1 | P23T-E | Human | Esophagus | ESCC | 7.44e-12 | 3.14e-01 | 0.108 |
| 154141 | MBOAT1 | P24T-E | Human | Esophagus | ESCC | 1.54e-02 | 7.92e-02 | 0.1287 |
| 154141 | MBOAT1 | P26T-E | Human | Esophagus | ESCC | 5.78e-05 | 1.19e-01 | 0.1276 |
| 154141 | MBOAT1 | P27T-E | Human | Esophagus | ESCC | 8.81e-04 | 1.86e-01 | 0.1055 |
| 154141 | MBOAT1 | P28T-E | Human | Esophagus | ESCC | 1.22e-12 | 2.50e-01 | 0.1149 |
| 154141 | MBOAT1 | P30T-E | Human | Esophagus | ESCC | 4.41e-11 | 3.65e-01 | 0.137 |
| 154141 | MBOAT1 | P31T-E | Human | Esophagus | ESCC | 4.52e-05 | 1.76e-01 | 0.1251 |
| 154141 | MBOAT1 | P36T-E | Human | Esophagus | ESCC | 4.17e-05 | 1.86e-01 | 0.1187 |
| 154141 | MBOAT1 | P37T-E | Human | Esophagus | ESCC | 3.53e-03 | 1.05e-01 | 0.1371 |
| 154141 | MBOAT1 | P39T-E | Human | Esophagus | ESCC | 3.55e-06 | 7.81e-02 | 0.0894 |
| 154141 | MBOAT1 | P40T-E | Human | Esophagus | ESCC | 3.18e-05 | 1.70e-01 | 0.109 |
| 154141 | MBOAT1 | P48T-E | Human | Esophagus | ESCC | 1.22e-08 | 1.19e-01 | 0.0959 |
| 154141 | MBOAT1 | P49T-E | Human | Esophagus | ESCC | 1.17e-11 | 5.16e-01 | 0.1768 |
| Page: 1 2 3 4 |
| Transcriptomic changes along malignancy continuum. |
| Tissue | Expression Dynamics | Abbreviation |
| Endometrium |  | AEH: Atypical endometrial hyperplasia |
| EEC: Endometrioid Cancer | ||
| 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 |
| ∗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 |
| 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). |
| Page: 1 2 3 4 5 6 7 8 9 |
| Enriched GO biological processes. |
| GO ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | Count |
| GO:00109758 | Endometrium | AEH | regulation of neuron projection development | 75/2100 | 445/18723 | 2.01e-04 | 2.54e-03 | 75 |
| GO:001097513 | Endometrium | EEC | regulation of neuron projection development | 79/2168 | 445/18723 | 6.80e-05 | 1.01e-03 | 79 |
| GO:000657521 | Liver | HCC | cellular modified amino acid metabolic process | 119/7958 | 188/18723 | 6.47e-09 | 1.67e-07 | 119 |
| GO:00086542 | Liver | HCC | phospholipid biosynthetic process | 150/7958 | 253/18723 | 4.77e-08 | 1.03e-06 | 150 |
| GO:00066444 | Liver | HCC | phospholipid metabolic process | 214/7958 | 383/18723 | 7.25e-08 | 1.48e-06 | 214 |
| GO:004648611 | Liver | HCC | glycerolipid metabolic process | 215/7958 | 392/18723 | 4.54e-07 | 7.49e-06 | 215 |
| GO:003025821 | Liver | HCC | lipid modification | 123/7958 | 212/18723 | 3.50e-06 | 4.58e-05 | 123 |
| GO:00066504 | Liver | HCC | glycerophospholipid metabolic process | 168/7958 | 306/18723 | 7.27e-06 | 8.62e-05 | 168 |
| GO:001097511 | Liver | HCC | regulation of neuron projection development | 220/7958 | 445/18723 | 1.68e-03 | 8.78e-03 | 220 |
| GO:00109756 | Lung | IAC | regulation of neuron projection development | 82/2061 | 445/18723 | 1.82e-06 | 8.78e-05 | 82 |
| GO:001097512 | Lung | AIS | regulation of neuron projection development | 69/1849 | 445/18723 | 1.05e-04 | 2.53e-03 | 69 |
| GO:00464701 | Lung | AIS | phosphatidylcholine metabolic process | 15/1849 | 74/18723 | 5.25e-03 | 4.49e-02 | 15 |
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| Enriched KEGG pathways. |
| Pathway ID | Tissue | Disease Stage | Description | Gene Ratio | Bg Ratio | pvalue | p.adjust | qvalue | Count |
| hsa005615 | Liver | HCC | Glycerolipid metabolism | 41/4020 | 63/8465 | 3.59e-03 | 1.12e-02 | 6.22e-03 | 41 |
| hsa0056112 | Liver | HCC | Glycerolipid metabolism | 41/4020 | 63/8465 | 3.59e-03 | 1.12e-02 | 6.22e-03 | 41 |
| Page: 1 |
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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 |
| Page: 1 |
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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. |
| Page: 1 |
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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 |
| MBOAT1 | SNV | Missense_Mutation | c.152N>A | p.Arg51His | p.R51H | Q6ZNC8 | protein_coding | deleterious(0) | probably_damaging(0.997) | TCGA-EW-A1IZ-01 | Breast | breast invasive carcinoma | Female | <65 | III/IV | Chemotherapy | taxotere | SD | |
| MBOAT1 | SNV | Missense_Mutation | c.1316N>T | p.Ala439Val | p.A439V | Q6ZNC8 | protein_coding | tolerated(0.4) | benign(0.047) | TCGA-C5-A7UH-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Chemotherapy | cisplatin | SD | |
| MBOAT1 | SNV | Missense_Mutation | rs199705606 | c.946G>A | p.Gly316Arg | p.G316R | Q6ZNC8 | protein_coding | deleterious(0) | probably_damaging(0.998) | TCGA-ZX-AA5X-01 | Cervix | cervical & endocervical cancer | Female | <65 | III/IV | Unknown | Unknown | SD |
| MBOAT1 | SNV | Missense_Mutation | c.1133N>T | p.Ala378Val | p.A378V | Q6ZNC8 | protein_coding | deleterious(0) | probably_damaging(0.981) | TCGA-AA-3956-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| MBOAT1 | SNV | Missense_Mutation | novel | c.842N>A | p.Arg281Gln | p.R281Q | Q6ZNC8 | protein_coding | tolerated(0.28) | benign(0.23) | TCGA-AA-3984-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD |
| MBOAT1 | SNV | Missense_Mutation | rs769390413 | c.1210N>A | p.Val404Ile | p.V404I | Q6ZNC8 | protein_coding | tolerated(0.43) | benign(0.009) | TCGA-AA-A010-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Chemotherapy | folinic | CR |
| MBOAT1 | SNV | Missense_Mutation | c.242G>A | p.Gly81Asp | p.G81D | Q6ZNC8 | protein_coding | deleterious(0) | probably_damaging(0.999) | TCGA-G4-6628-01 | Colorectum | colon adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | SD | |
| MBOAT1 | deletion | Frame_Shift_Del | c.1331delN | p.Leu444TrpfsTer20 | p.L444Wfs*20 | Q6ZNC8 | protein_coding | TCGA-AA-3663-01 | Colorectum | colon adenocarcinoma | Male | <65 | I/II | Unknown | Unknown | SD | |||
| MBOAT1 | insertion | Frame_Shift_Ins | novel | c.213_214insT | p.Gly72TrpfsTer31 | p.G72Wfs*31 | Q6ZNC8 | protein_coding | TCGA-AA-3947-01 | Colorectum | colon adenocarcinoma | Female | <65 | I/II | Unknown | Unknown | SD | ||
| MBOAT1 | deletion | Frame_Shift_Del | c.108delN | p.Phe36LeufsTer57 | p.F36Lfs*57 | Q6ZNC8 | protein_coding | TCGA-AG-A00Y-01 | Colorectum | rectum adenocarcinoma | Male | >=65 | I/II | Unknown | Unknown | PD |
| Page: 1 2 3 4 5 6 7 |
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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 |
| Page: 1 |
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