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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
Facial palsy
Difficulty walking
Disease(s) Associated with SLC18A3
congenital myasthenic syndrome 21

Mouse Phenotypes
increased susceptibility to pharmacologically induced seizures
increased acetylcholine level
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
Chat/Slc18a3tm1.1Vpra/Chat/Slc18a3tm1.1Vpra
Chat/Slc18a3tm1Vpra/Chat/Slc18a3tm1Vpra
Slc18a3tm1Mca/Slc18a3tm1Mca
Chat/Slc18a3tm1.1Vpra/Slc18a3+
Chat/Slc18a3tm1Vpra/Chat/Slc18a3tm1.1Vpra
Slc18a3tm1Mca/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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Funding Information
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last database update
07/29/2020
MGI 6.15
The Jackson Laboratory