Cell Senescence Entries for MDM2
- Cell Types
- Glioblastoma
- Cell Lines
- U-373MG
- Cancer Cell?
- Yes
- Method
- Knockdown
- Type of senescence
- Unclear
- Senescence Effect
- Inhibits
- Primary Reference
- Kovatcheva et al. (2016) MDM2 turnover and expression of ATRX determine the choice between quiescence and senescence in response to CDK4 inhibition. Oncotarget 6(10)8226-43 (PubMed)
MDM2 Gene Information
- HGNC symbol
- MDM2
- Aliases
- HDM2; MGC5370
- Common name
- MDM2 proto-oncogene
- Entrez Id
- 4193
- Description
- This gene encodes a nuclear-localized E3 ubiquitin ligase. The encoded protein can promote tumor formation by targeting tumor suppressor proteins, such as p53, for proteasomal degradation. This gene is itself transcriptionally-regulated by p53. Overexpression or amplification of this locus is detected in a variety of different cancers. There is a pseudogene for this gene on chromosome 2. Alternative splicing results in a multitude of transcript variants, many of which may be expressed only in tumor cells. [provided by RefSeq, Jun 2013].
MDM2 Ontologies
- Gene Ontology
-
Process: GO:43066; negative regulation of apoptotic process
GO:16567; protein ubiquitination
GO:6915; apoptotic process
GO:45892; negative regulation of transcription, DNA-templated
GO:122; negative regulation of transcription by RNA polymerase II
GO:51865; protein autoubiquitination
GO:6511; ubiquitin-dependent protein catabolic process
GO:51726; regulation of cell cycle
GO:6357; regulation of transcription by RNA polymerase II
GO:42176; regulation of protein catabolic process
GO:16925; protein sumoylation
GO:31648; protein destabilization
GO:8284; positive regulation of cell population proliferation
GO:65003; protein-containing complex assembly
GO:32436; positive regulation of proteasomal ubiquitin-dependent protein catabolic process
GO:34504; protein localization to nucleus
GO:71456; cellular response to hypoxia
GO:43518; negative regulation of DNA damage response, signal transduction by p53 class mediator
GO:46677; response to antibiotic
GO:45931; positive regulation of mitotic cell cycle
GO:71480; cellular response to gamma radiation
GO:72717; cellular response to actinomycin D
GO:1990000; amyloid fibril formation
GO:45184; establishment of protein localization
GO:36369; transcription factor catabolic process
GO:6977; DNA damage response, signal transduction by p53 class mediator resulting in cell cycle arrest
GO:209; protein polyubiquitination
GO:1568; blood vessel development
GO:1974; blood vessel remodeling
GO:2027; regulation of heart rate
GO:3170; heart valve development
GO:3181; atrioventricular valve morphogenesis
GO:3203; endocardial cushion morphogenesis
GO:3281; ventricular septum development
GO:3283; atrial septum development
GO:7089; traversing start control point of mitotic cell cycle
GO:7507; heart development
GO:10468; regulation of gene expression
GO:43161; proteasome-mediated ubiquitin-dependent protein catabolic process
GO:45787; positive regulation of cell cycle
GO:51149; positive regulation of muscle cell differentiation
GO:51603; proteolysis involved in cellular protein catabolic process
GO:60411; cardiac septum morphogenesis
GO:1901797; negative regulation of signal transduction by p53 class mediator
GO:1902254; negative regulation of intrinsic apoptotic signaling pathway by p53 class mediator
GO:65008; regulation of biological quality
Cellular component: GO:5634; nucleus
GO:5737; cytoplasm
GO:32991; protein-containing complex
GO:5730; nucleolus
GO:5654; nucleoplasm
GO:5886; plasma membrane
GO:5829; cytosol
GO:17053; transcription repressor complex
GO:30666; endocytic vesicle membrane
GO:16604; nuclear body
Function: GO:5515; protein binding
GO:46872; metal ion binding
GO:16740; transferase activity
GO:8270; zinc ion binding
GO:31625; ubiquitin protein ligase binding
GO:16874; ligase activity
GO:61630; ubiquitin protein ligase activity
GO:4842; ubiquitin-protein transferase activity
GO:43130; ubiquitin binding
GO:19899; enzyme binding
GO:42802; identical protein binding
GO:19904; protein domain specific binding
GO:43021; ribonucleoprotein complex binding
GO:19789; SUMO transferase activity
GO:2039; p53 binding
GO:97718; disordered domain specific binding
GO:47485; protein N-terminus binding
GO:8097; 5S rRNA binding
GO:61663; NEDD8 ligase activity
Homologs of MDM2 in Model Organisms
In other databases
- GenAge human genes
- This gene is present as MDM2
- LongevityMap
- This gene is present as MDM2
- CellAge gene expression
- This gene is present as MDM2
External links
- OMIM
- 164785
- Ensembl
- ENSG00000135679
- Entrez Gene
- 4193
- UniGene
- 733536
- 1000 Genomes
- 1000 Genomes
- HPRD
- GenAtlas
- MDM2
- GeneCards
- MDM2