Symbol Name ID |
Sncg
synuclein, gamma MGI:1298397 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Lewy bodies |
Parkinsonism |
Delusion |
Visual hallucination |
Dementia |
Fluctuations in consciousness |
Disease(s) Associated with SNCG | ||||||
Lewy body dementia |
Mouse Phenotypes | nervous system phenotype |
decreased susceptibility to dopaminergic neuron neurotoxicity |
microgliosis |
abnormal nervous system morphology |
astrocytosis |
gliosis |
decreased dopaminergic neuron number |
decreased motor neuron number |
abnormal myelin sheath morphology |
neuron degeneration |
abnormal trigeminal nerve morphology |
abnormal dorsal spinal root morphology |
abnormal sciatic nerve morphology |
abnormal ventral spinal root morphology |
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Availability | Mouse Genotype | ||||||||||||||
Sncgtm1Vlb/Sncgtm1Vlb | * | ||||||||||||||
Tg(Thy1-Sncg)HvP36Putt/Tg(Thy1-Sncg)HvP36Putt | |||||||||||||||
Tg(Thy1-Sncg)HvP36Putt/0 | |||||||||||||||
Tg(Thy1-Sncg)HvP36Putt/? | * |
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 05/07/2024 MGI 6.23 |
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