Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   

Ontology Browser

Term:
regulation of mitotic G1 cell cycle arrest in response to nitrogen starvation (GO:1903693)
Annotations: Rat: (0) Mouse: (0) Human: (0) Chinchilla: (0) Bonobo: (0) Dog: (0) Squirrel: (0) Pig: (0)
Parent Terms Term With Siblings Child Terms
negative regulation of cell communication +   
negative regulation of cell cycle arrest  
negative regulation of cellular response to nitrogen starvation 
negative regulation of mitochondrial unfolded protein response by negative regulation of transcription from RNA polymerase II promoter 
negative regulation of mitotic cell cycle +   
negative regulation of response to nutrient levels +   
positive regulation of cell communication +   
positive regulation of cell cycle arrest +   
positive regulation of mitotic cell cycle +   
positive regulation of mitotic G1 cell cycle arrest in response to nitrogen starvation 
positive regulation of response to nutrient levels +   
priming of cellular response to stress 
regulation of aggregation involved in sorocarp development +  
regulation of AV node cell action potential +   
regulation of BMP secretion +  
regulation of c-di-GMP signaling +  
regulation of cell communication by chemical coupling +   
regulation of cell communication by electrical coupling +   
regulation of cell communication involved in growth plate cartilage morphogenesis 
regulation of cell cycle switching, mitotic to meiotic cell cycle +  
regulation of cellular response to amino acid starvation +  
regulation of cellular response to glucose starvation 
regulation of cellular response to heat +   
regulation of cellular response to hypoxia +   
regulation of cellular response to iron ion starvation +  
regulation of cellular response to osmotic stress +   
regulation of cellular response to oxidative stress +   
regulation of cellular response to phosphate starvation +  
regulation of cellular senescence +   
regulation of eIF2 alpha phosphorylation by dsRNA  
regulation of eIF2 alpha phosphorylation by heme  
regulation of establishment of competence for transformation +  
regulation of filamentous growth of a population of unicellular organisms in response to starvation +  
regulation of hormone secretion +   
regulation of induction of conjugation upon nitrogen starvation 
regulation of mitotic cell cycle DNA replication +   
regulation of mitotic cell cycle phase transition +   
regulation of mitotic cell cycle, embryonic +   
regulation of mitotic cohesin unloading +  
regulation of mitotic DNA damage checkpoint +   
regulation of mitotic G1 cell cycle arrest in response to nitrogen starvation +  
Any process that modulates the frequency, rate or extent of mitotic G1 cell cycle arrest in response to nitrogen starvation.
regulation of mitotic nuclear division +   
regulation of mitotic spindle checkpoint +   
regulation of neuron projection regeneration +   
regulation of nitrosative stress-induced intrinsic apoptotic signaling pathway +   
regulation of parkin-mediated stimulation of mitophagy in response to mitochondrial depolarization +   
regulation of plant-type hypersensitive response +  
regulation of Purkinje myocyte action potential  
regulation of response to DNA damage stimulus +   
regulation of response to endoplasmic reticulum stress +   
regulation of response to food +   
regulation of SA node cell action potential  
regulation of signal transduction +   
regulation of SREBP signaling pathway +   
regulation of stress-activated protein kinase signaling cascade +   
regulation of synaptic signaling by nitric oxide 
regulation of trans-synaptic signaling +   
regulation of transmission of nerve impulse +   
regulation of trichome patterning +  
regulation of vitamin D receptor signaling pathway +   
regulation of Wnt protein secretion +   

Synonyms
Definition Sources: GO_REF:0000058, GOC:TermGenie, PMID:15713656

paths to the root

NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.