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Symbol
Name
ID

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

Phenotype annotations related to nervous system

Darker colors indicate more annotations

Human Phenotypes	Difficulty walking	Easy fatigability	Fatigable weakness of skeletal muscles	Hyperintensity of cerebral white matter on MRI
Disease(s) Associated with SLC18A3
congenital myasthenic syndrome 21

Mouse Phenotypes		increased susceptibility to pharmacologically induced seizures	abnormal motor neuron innervation pattern	increased motor neuron number	abnormal neuromuscular synapse morphology	abnormal endplate potential	abnormal miniature endplate potential	abnormal synaptic acetylcholine release
Availability	Mouse Genotype		abnormal motor neuron innervation pattern	increased motor neuron number	abnormal neuromuscular synapse morphology	abnormal endplate potential	abnormal miniature endplate potential	abnormal synaptic acetylcholine release
	Chat/Slc18a3^tm1.1Vpra/Chat/Slc18a3^tm1.1Vpra
	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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