HCSGD entry for MYH9
1. General information
Official gene symbol | MYH9 |
---|---|
Entrez ID | 4627 |
Gene full name | myosin, heavy chain 9, non-muscle |
Other gene symbols | BDPLT6 DFNA17 EPSTS FTNS MHA NMHC-II-A NMMHC-IIA NMMHCA |
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:0000146 | Microfilament motor activity | IDA | molecular_function |
GO:0000212 | Meiotic spindle organization | IEA | biological_process |
GO:0000904 | Cell morphogenesis involved in differentiation | IEA | biological_process |
GO:0000910 | Cytokinesis | IMP | biological_process |
GO:0001525 | Angiogenesis | IDA | biological_process |
GO:0001701 | In utero embryonic development | IEA | biological_process |
GO:0001725 | Stress fiber | IDA | cellular_component |
GO:0001726 | Ruffle | IDA | cellular_component |
GO:0001768 | Establishment of T cell polarity | IEA | biological_process |
GO:0001772 | Immunological synapse | IDA IEA | cellular_component |
GO:0001931 | Uropod | IDA IEA | cellular_component |
GO:0003774 | Motor activity | IEA NAS | molecular_function |
GO:0003779 | Actin binding | IDA IEA | molecular_function |
GO:0005515 | Protein binding | IPI | molecular_function |
GO:0005516 | Calmodulin binding | IEA | molecular_function |
GO:0005524 | ATP binding | IDA IEA | molecular_function |
GO:0005634 | Nucleus | IDA | cellular_component |
GO:0005737 | Cytoplasm | IDA | cellular_component |
GO:0005819 | Spindle | IEA | cellular_component |
GO:0005826 | Actomyosin contractile ring | IDA | cellular_component |
GO:0005829 | Cytosol | IDA | cellular_component |
GO:0005886 | Plasma membrane | IDA | cellular_component |
GO:0005913 | Cell-cell adherens junction | IEA | cellular_component |
GO:0006200 | ATP catabolic process | IDA | biological_process |
GO:0006509 | Membrane protein ectodomain proteolysis | IDA | biological_process |
GO:0006928 | Cellular component movement | IEA | biological_process |
GO:0007229 | Integrin-mediated signaling pathway | NAS | biological_process |
GO:0007411 | Axon guidance | TAS | biological_process |
GO:0007520 | Myoblast fusion | IEA | biological_process |
GO:0008180 | COP9 signalosome | IDA | cellular_component |
GO:0008305 | Integrin complex | IDA | cellular_component |
GO:0008360 | Regulation of cell shape | IMP | biological_process |
GO:0015031 | Protein transport | IMP | biological_process |
GO:0015629 | Actin cytoskeleton | IDA | cellular_component |
GO:0016337 | Cell-cell adhesion | IEA | biological_process |
GO:0016459 | Myosin complex | IEA | cellular_component |
GO:0016460 | Myosin II complex | IEA | cellular_component |
GO:0016887 | ATPase activity | IDA | molecular_function |
GO:0030048 | Actin filament-based movement | IDA | biological_process |
GO:0030220 | Platelet formation | IMP | biological_process |
GO:0030224 | Monocyte differentiation | IEP | biological_process |
GO:0030863 | Cortical cytoskeleton | IEA | cellular_component |
GO:0030898 | Actin-dependent ATPase activity | IDA | molecular_function |
GO:0031252 | Cell leading edge | IDA | cellular_component |
GO:0031532 | Actin cytoskeleton reorganization | IMP | biological_process |
GO:0031594 | Neuromuscular junction | IEA | cellular_component |
GO:0032154 | Cleavage furrow | IDA | cellular_component |
GO:0032796 | Uropod organization | IEA | biological_process |
GO:0038032 | Termination of G-protein coupled receptor signaling pathway | IEA | biological_process |
GO:0042803 | Protein homodimerization activity | IDA | molecular_function |
GO:0043234 | Protein complex | IDA | cellular_component |
GO:0043495 | Protein anchor | IMP | molecular_function |
GO:0043531 | ADP binding | IDA | molecular_function |
GO:0043534 | Blood vessel endothelial cell migration | IMP | biological_process |
GO:0050900 | Leukocyte migration | NAS | biological_process |
GO:0051015 | Actin filament binding | IDA IEA NAS | molecular_function |
GO:0051295 | Establishment of meiotic spindle localization | IEA | biological_process |
GO:0070062 | Extracellular vesicular exosome | IDA | cellular_component |
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4. Expression levels in datasets
- Meta-analysis result
p-value up | p-value down | FDR up | FDR down |
---|---|---|---|
0.6434765055 | 0.0222300596 | 0.9999902473 | 0.2864271659 |
- 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 | Down | -1.6013373435 |
GSE13712_SHEAR | Down | -0.1306829439 |
GSE13712_STATIC | Down | -0.2132262616 |
GSE19018 | Up | 0.6039049990 |
GSE19899_A1 | Down | -1.0055834303 |
GSE19899_A2 | Down | -0.4480227786 |
PubMed_21979375_A1 | Down | -0.7386290195 |
PubMed_21979375_A2 | Up | 0.0678388022 |
GSE35957 | Down | -0.4007328579 |
GSE36640 | Down | -0.5704577191 |
GSE54402 | Down | -0.0540421774 |
GSE9593 | Up | 0.0029210823 |
GSE43922 | Down | -0.4708264187 |
GSE24585 | Down | -0.1049308661 |
GSE37065 | Down | -0.3857233184 |
GSE28863_A1 | Up | 0.3691932254 |
GSE28863_A2 | Up | 0.4560034712 |
GSE28863_A3 | Up | 0.3149589218 |
GSE28863_A4 | Up | 0.1312116971 |
GSE48662 | Down | -0.1383544074 |
5. Regulation relationships with compounds/drugs/microRNAs
- Compounds
Not regulated by compounds
- Drugs
Not regulated by drugs
- MicroRNAs
- mirTarBase
MiRNA_name | mirBase ID | miRTarBase ID | Experiment | Support type | References (Pubmed ID) |
---|---|---|---|---|---|
hsa-miR-124-3p | MIMAT0000422 | MIRT002579 | Microarray | Functional MTI (Weak) | 15685193 |
hsa-miR-124-3p | MIMAT0000422 | MIRT002579 | Proteomics;Microarray | Non-Functional MTI (Weak) | 18668037 |
hsa-miR-9-5p | MIMAT0000441 | MIRT021471 | Microarray | Functional MTI (Weak) | 17612493 |
hsa-miR-1296-5p | MIMAT0005794 | MIRT036109 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-877-3p | MIMAT0004950 | MIRT037181 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-193b-3p | MIMAT0002819 | MIRT041494 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-484 | MIMAT0002174 | MIRT042190 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-324-3p | MIMAT0000762 | MIRT042922 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-331-3p | MIMAT0000760 | MIRT043426 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-149-5p | MIMAT0000450 | MIRT045466 | CLASH | Functional MTI (Weak) | 23622248 |
hsa-miR-92a-3p | MIMAT0000092 | MIRT049384 | 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: 5 abstracts the gene occurs.
PubMed ID of the article | Sentenece the gene occurs |
---|---|
26152646 | Estimated glomerular filtration rate (eGFR), 25(OH) D3, chronic kidney disease (CKD), the MYH9 (myosin heavy chain 9) gene in old and very elderly people |
26152646 | This does not mean that there is no physiological ageing process at all; in addition to those already elucidated, its mechanisms include cell senescence, podocyte dysfunction, a vitamin D deficiency, and homozygotic forms of the MYH9 gene |
26152646 | 73 m(2), plasma 25(OH)D3 levels and the MYH9 gene in a population of elderly and very elderly persons |
26152646 | Here we observed a lower Hb level and an elevated Alb/Cr ratio in subjects heterozygotic for the MYH9 gene |
26152646 | This could be interpreted in the sense that the gene could exert some protective effect on renal function, whereas the heterozygotic form (allele A) of the MYH9 gene could be considered a very early marker, a new risk factor for the appearance of CKD, or a sign of renal frailty in elderly people |
24862015 | The central idea described here is the concept called the membrane hypothesis of aging (MHA) |
24862015 | This chapter covers also the available anti-aging interventions on the cell membrane by means of the centrophenoxine treatment based on the MHA |
23974104 | Drug affinity responsive target stability (DARTS) analysis identified IQ motif-containing factors IQGAP1 and MYH9 as direct binding targets of disulfiram |
15374458 | This review summarizes the main points of an interdisciplinary, theoretically established approach to the problem of cell senescence, called membrane hypothesis of aging (MHA) |
15374458 | It is emphasized that MHA is not an alternative to the other aging hypotheses but represents a synthesis of most of them |
15374458 | It is pointed out that the new drug design based on the MHA resulted in a useful new molecule which is able to improve the key cell parameters deteriorated by advancing age |
2653255 | According to the membrane hypothesis of aging (MHA), cellular senescence is attributable to a life-long, cross-linking action of oxygen-free radicals in the cell plasma membrane, resulting in a continuous decrease of the passive ion permeabilities |
2653255 | MHA suggested that an age-dependent increase in the physical density of the intracellular mass can underly the well-known age-dependent decreases of the macromolecular synthetic processes, the enzymic turnover rates, etc |
2653255 | MHA was partly based on a molecular enzyme kinetic model (MEKM) suggesting that environmental factors can substantially influence the enzyme catalysis and regulation through collisional coupling |
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