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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Syn1
synapsin I
MGI:98460
8 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Syn1tm1Pggd/Syn1tm1Pggd
Syn2tm1Pggd/Syn2tm1Pggd
involves: 129P2/OlaHsd
abnormal CNS synapse formation J:91113
normal nervous system phenotype J:91113
Syn1tm1Pggd/Syn1tm1Pggd
Syn2tm1Pggd/Syn2tm1Pggd
Syn3tm1Pggd/Syn3tm1Pggd
involves: 129 * 129P2/OlaHsd * 129X1/SvJ * C57BL/6
abnormal brain wave pattern J:175256
environmentally induced seizures J:175256
tonic-clonic seizures J:175256
Syn1tm1Sud/Syn1tm1Sud
Syn2tm1Sud/Syn2tm1Sud
involves: 129S7/SvEvBrd
convulsive seizures J:26920
decreased post-tetanic potentiation J:26920
increased synaptic depression J:26920
Syn1tm1Sud/Syn1tm1Sud
Tg(Camk2a-HRAS*G12V)1Sva/0
involves: 129S7/SvEvBrd * 129T2/SvEmsJ * C57BL/6 * C57BL/6N
normal nervous system phenotype J:102160

Contributing Projects:
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
11/12/2024
MGI 6.24
The Jackson Laboratory