Symbol Name ID |
Nr4a2
nuclear receptor subfamily 4, group A, member 2 MGI:1352456 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Hyposmia |
Spasticity |
Bradykinesia |
Tremor |
Depression |
Anxiety |
Panic attack |
Hallucinations |
Apathy |
Reduced social reciprocity |
Impulsivity |
Agitation |
Restless legs |
Cognitive impairment |
Dementia |
Frontal lobe dementia |
Short attention span |
Insomnia |
Hyperreflexia |
Dyskinesia |
Dystonia |
Gait imbalance |
Postural instability |
Abnormal autonomic nervous system physiology |
Disease(s) Associated with NR4A2 | ||||||||||||||||||||||||
Parkinson's disease |
Mouse Phenotypes | nervous system phenotype |
increased midbrain apoptosis |
abnormal midbrain development |
abnormal substantia nigra morphology |
abnormal tegmentum morphology |
abnormal nervous system development |
abnormal dopaminergic neuron morphology |
decreased dopaminergic neuron number |
loss of dopaminergic neurons |
neuron degeneration |
|
Availability | Mouse Genotype | ||||||||||
Nr4a2tm1Niko/Nr4a2tm1Niko | * | ||||||||||
Nr4a2tm1Omc/Nr4a2tm1Omc | |||||||||||
Nr4a2tm1Tpe/Nr4a2tm1Tpe | |||||||||||
Nr4a2tm1Omc/Nr4a2+ | |||||||||||
Nr4a2tm1.1Pcn/Nr4a2tm1.1Pcn Slc6a3tm1(cre)Lrsn/Slc6a3tm1(cre)Lrsn (conditional) |
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Nr4a2tm1.1Pcn/Nr4a2tm1.1Pcn (conditional) | * |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 04/23/2024 MGI 6.23 |
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