Symbol Name ID |
Snca
synuclein, alpha MGI:1277151 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Orthostatic hypotension |
Dysphagia |
Gliosis |
Lewy bodies |
Global brain atrophy |
Bradykinesia |
Parkinsonism |
Myoclonus |
Resting tremor |
Dysarthria |
Depression |
Paranoia |
Delusion |
Hallucinations |
Visual hallucination |
Mental deterioration |
Dementia |
Micrographia |
Fluctuations in consciousness |
Sleep abnormality |
Hypokinesia |
Dystonia |
Gait disturbance |
Loss of ambulation |
Shuffling gait |
Postural instability |
Abnormal autonomic nervous system physiology |
Disease(s) Associated with SNCA | |||||||||||||||||||||||||||
Lewy body dementia | |||||||||||||||||||||||||||
Parkinson's disease 1 | |||||||||||||||||||||||||||
Parkinson's disease 4 |
Mouse Phenotypes | nervous system phenotype |
decreased susceptibility to dopaminergic neuron neurotoxicity |
microgliosis |
abnormal brainstem morphology |
astrocytosis |
abnormal neuron morphology |
abnormal dopaminergic neuron morphology |
decreased dopaminergic neuron number |
abnormal motor neuron morphology |
abnormal axon morphology |
abnormal dendrite morphology |
abnormal neuromuscular synapse morphology |
abnormal spinal cord morphology |
alpha-synuclein inclusion body |
axon degeneration |
demyelination |
abnormal synaptic transmission |
reduced long-term potentiation |
abnormal miniature excitatory postsynaptic currents |
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Availability | Mouse Genotype | |||||||||||||||||||
Sncatm1Rosl/Sncatm1Rosl | * | |||||||||||||||||||
Sncatm1Sud/Sncatm1Sud | ||||||||||||||||||||
Sncatm1Wtd/Sncatm1Wtd | ||||||||||||||||||||
Tg(THY1-Snca)M1mSud/0 | * | |||||||||||||||||||
Tg(Thy1-Snca)1S13Putt/? |
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 05/21/2024 MGI 6.23 |
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