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Symbol
Name
ID

Syt2
synaptotagmin II
MGI:99666

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Decreased fetal movement	Feeding difficulties	Nasal regurgitation	Poor suck	Choking episodes	Weak cry	Dysphonia	Hypernasal speech
Disease(s) Associated with SYT2
congenital myasthenic syndrome

Mouse Phenotypes		abnormal motor capabilities/coordination/movement	tremors	ataxia	impaired coordination	abnormal locomotor behavior
Availability	Mouse Genotype	abnormal motor capabilities/coordination/movement	tremors	ataxia	impaired coordination	abnormal locomotor behavior
	Syt2^m1Btlr/Syt2^m1Btlr
	Syt2^m1Ingm/Syt2^m1Ingm
	Syt2^tm1Sud/Syt2^tm1Sud

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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