Symbol Name ID |
Fyn
Fyn proto-oncogene MGI:95602 |
Darker colors indicate more annotations |
Human Phenotypes | EEG abnormality |
Delusion |
Schizophrenia |
Hallucinations |
Negativism |
Social and occupational deterioration |
Disease(s) Associated with FYN | ||||||
schizophrenia |
Mouse Phenotypes | increased susceptibility to pharmacologically induced seizures |
abnormal seizure response to electrical stimulation |
abnormal kindling response |
audiogenic seizures |
tonic seizures |
decreased corpus callosum size |
abnormal hypothalamus morphology |
abnormal hippocampus morphology |
abnormal dentate gyrus morphology |
abnormal hippocampus layer morphology |
abnormal hippocampus pyramidal cell layer |
abnormal hippocampus pyramidal cell morphology |
ectopic hippocampus pyramidal cells |
increased hippocampus pyramidal cell number |
abnormal somatosensory cortex morphology |
abnormal stratification in cerebral cortex |
abnormal olfactory bulb morphology |
abnormal optic nerve morphology |
abnormal myelination |
abnormal excitatory postsynaptic potential |
reduced long-term potentiation |
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Availability | Mouse Genotype | |||||||||||||||||||||
Fyntm1Fam/Fyntm1Fam | ||||||||||||||||||||||
Fyntm1Sor/Fyntm1Sor | ||||||||||||||||||||||
Fyntm1Sor/Fyntm1Sor Tg(Camk2a-Fyn)1Kndl/0 |
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Fyntm1Yik/Fyntm1Yik | ||||||||||||||||||||||
Fyntm1Sor/Fyn+ Tg(Camk2a-Fyn-531)1Nko/0 |
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Tg(Camk2a-Fyn-531)1Nko/0 |
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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