HCSGD entry for MUT
1. General information
| Official gene symbol | MUT |
|---|---|
| Entrez ID | 4594 |
| Gene full name | methylmalonyl CoA mutase |
| Other gene symbols | MCM |
| Links to Entrez Gene | Links to Entrez Gene |
2. Neighbors in the network
This gene isn't in Literature mining network.
3. Gene ontology annotation
GO ID | GO term | Evidence | Category |
|---|---|---|---|
| GO:0004494 | Methylmalonyl-CoA mutase activity | IEA | molecular_function |
| GO:0005739 | Mitochondrion | TAS | cellular_component |
| GO:0005759 | Mitochondrial matrix | TAS | cellular_component |
| GO:0006635 | Fatty acid beta-oxidation | TAS | biological_process |
| GO:0006766 | Vitamin metabolic process | TAS | biological_process |
| GO:0006767 | Water-soluble vitamin metabolic process | TAS | biological_process |
| GO:0009235 | Cobalamin metabolic process | TAS | biological_process |
| GO:0009791 | Post-embryonic development | IEA | biological_process |
| GO:0019626 | Short-chain fatty acid catabolic process | TAS | biological_process |
| GO:0031419 | Cobalamin binding | IEA | molecular_function |
| GO:0044255 | Cellular lipid metabolic process | TAS | biological_process |
| GO:0044281 | Small molecule metabolic process | TAS | biological_process |
| GO:0046872 | Metal ion binding | IEA | molecular_function |
| GO:0050667 | Homocysteine metabolic process | IDA | biological_process |
| GO:0072341 | Modified amino acid binding | IDA | molecular_function |
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4. Expression levels in datasets
- Meta-analysis result
| p-value up | p-value down | FDR up | FDR down |
|---|---|---|---|
| 0.9806337715 | 0.0063940770 | 0.9999902473 | 0.1630028019 |
- Individual experiment result
( "-" represent NA in the specific microarray platform )
( "-" represent NA in the specific microarray platform )
| Data source | Up or down | Log fold change |
|---|---|---|
| GSE11954 | Up | 0.1593518941 |
| GSE13712_SHEAR | Down | -0.3491104091 |
| GSE13712_STATIC | Down | -0.4132203889 |
| GSE19018 | Up | 0.0348144688 |
| GSE19899_A1 | Down | -0.9737628469 |
| GSE19899_A2 | Down | -0.8548789299 |
| PubMed_21979375_A1 | Down | -0.8213721303 |
| PubMed_21979375_A2 | Down | -0.7834688929 |
| GSE35957 | Down | -0.3647169358 |
| GSE36640 | Down | -0.2897667320 |
| GSE54402 | Down | -0.7069482570 |
| GSE9593 | Up | 0.0730940950 |
| GSE43922 | Down | -0.6405658893 |
| GSE24585 | Up | 0.2353329890 |
| GSE37065 | Up | 0.0272613600 |
| GSE28863_A1 | Up | 0.0145701747 |
| GSE28863_A2 | Up | 0.2750916657 |
| GSE28863_A3 | Down | -1.2383990490 |
| GSE28863_A4 | Down | -0.3249126179 |
| GSE48662 | Up | 0.0721940418 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Name | Drug | Accession number |
|---|---|---|
| Cyanocobalamin | DB00115 | NUTR00004 | APRD00326 | EXPT00965 |
| Hydroxocobalamin | DB00200 | APRD01022 |
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
|---|---|---|---|---|---|
| hsa-miR-155-5p | MIMAT0000646 | MIRT020551 | Proteomics | Functional MTI (Weak) | 18668040 |
| hsa-miR-615-3p | MIMAT0003283 | MIRT039809 | CLASH | Functional MTI (Weak) | 23622248 |
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- mirRecord
No target information from mirRecord
6. Text-mining results about the gene
Gene occurances in abstracts of cellular senescence-associated articles: 4 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
|---|---|
| 27651846 | Cells were seeded into 24-well plates with hydrogen peroxide added to cell medium and incubated at 37 degrees C + 5% CO2 for a 90-minute period [at 0, 300, 400 and 800 micromolar (MCM) hydrogen peroxide] |
| 27651846 | Treatment with hydrogen peroxide reduced this level of cell proliferation significantly (to 52,167 cells at 400 MCM; to 49,263 cells at 800 MCM) |
| 27651846 | Meanwhile, cells with a high level of positive senescence-indicator SA-Beta-Gal-positive staining was induced by hydrogen peroxide treatment (from a baseline level of 12% to 80% at 400 MCM and at 800 MCM) |
| 22790201 | Human Mut T Homolog 1 (MTH1): a roadblock for the tumor-suppressive effects of oncogenic RAS-induced ROS |
| 21160097 | The MCM (minichromosome maintenance protein) protein family was identified for the first time in budding yeast, Saccharomyces cerevisiae |
| 21160097 | The subgroup consists of MCM proteins 2-9, that possess the characteristic ATPase domain (MCM box) |
| 21160097 | There are also MCM1 and MCM10, which are important in DNA replication, but they do not possess the specific MCM box |
| 21160097 | The main function of MCM proteins is cooperation with other factors in molecular mechanisms that form the replication fork and in regulation of DNA synthesis |
| 21160097 | MCM proteins form a ring-shaped complex, which is activated when other factors are bound |
| 21160097 | MCM 2-7 complex is one of the pre-replication factors |
| 21160097 | Association of MCM 2-7 complex is a crucial moment initiating the replication fork |
| 21160097 | MCM proteins play a role in maintaining genome integrity and prevent re-replication once per cell cycle |
| 21160097 | Proliferating cells have high levels of MCM, whereas they are not detected in quiescent, differentiated or senescent cells |
| 21160097 | The aim of this work is to summarize current knowledge about the role of MCM proteins in DNA replication and potential diagnostic markers of proliferating cancer cells |
| 19001876 | In eukaryotic cells, MCM, the minichromosome maintenance proteins, form a heterohexamer during G(1) phase in the cell cycle and constitute a DNA helicase activity at the onset of replication |
| 19001876 | MCM proteins are downregulated and dissociated from chromatin when cells exit the cell cycle |
| 19001876 | MCM proteins are upregulated frequently in a variety of dysplastic and cancer cells |
| 19001876 | To delineate the role of MCM in esophageal epithelial biology, we determined the MCM family gene expression during cellular senescence, immortalization, differentiation and apoptosis |
| 19001876 | Epitope mapping of this MCM2-related fragment suggested the lack of amino- and carboxyl-terminal regions, including one of the putative nuclear localization signals and the ATPase domain, the MCM box |
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