Syn2 Phenotype Annotations - Multigenic Genotypes

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Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Syn2
synapsin II
MGI:103020

8 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Syn1^tm1Pggd/Syn1^tm1Pggd Syn2^tm1Pggd/Syn2^tm1Pggd involves: 129P2/OlaHsd	abnormal CNS synapse formation	J:91113
	normal nervous system phenotype	J:91113
Syn1^tm1Pggd/Syn1^tm1Pggd Syn2^tm1Pggd/Syn2^tm1Pggd Syn3^tm1Pggd/Syn3^tm1Pggd involves: 129 * 129P2/OlaHsd * 129X1/SvJ * C57BL/6	abnormal brain wave pattern	J:175256
	environmentally induced seizures	J:175256
	tonic-clonic seizures	J:175256
Syn1^tm1Sud/Syn1^tm1Sud Syn2^tm1Sud/Syn2^tm1Sud involves: 129S7/SvEvBrd	convulsive seizures	J:26920
	decreased post-tetanic potentiation	J:26920
	increased synaptic depression	J:26920

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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