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Symbol
Name
ID

Slc18a3
solute carrier family 18 (vesicular monoamine), member 3
MGI:1101061

Phenotype annotations related to behavior/neurological

*	Aspects of the system are reported to show a normal phenotype.
	Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties	Fatigue
Disease(s) Associated with SLC18A3	Feeding difficulties	Fatigue
congenital myasthenic syndrome 21

Mouse Phenotypes		behavior/neurological phenotype	increased susceptibility to pharmacologically induced seizures	abnormal object recognition memory	impaired coordination	decreased grip strength	increased vertical activity	hyperactivity	abnormal social investigation	impaired exercise endurance
Availability	Mouse Genotype	behavior/neurological phenotype		abnormal object recognition memory	impaired coordination	decreased grip strength	increased vertical activity	hyperactivity	abnormal social investigation	impaired exercise endurance
	Chat/Slc18a3^tm1.2Vpra/Chat/Slc18a3^tm1.2Vpra	*
	Chat/Slc18a3^tm1Vpra/Chat/Slc18a3^tm1Vpra	*
	Slc18a3^tm1Mca/Slc18a3^tm1Mca
	Chat/Slc18a3^tm1.1Vpra/Slc18a3⁺	*
	Chat/Slc18a3^tm1Vpra/Chat/Slc18a3^tm1.1Vpra	*
	Slc18a3^tm1Mca/Slc18a3⁺	*

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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