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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
Disease(s) Associated with SLC18A3
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
Chat/Slc18a3tm1.2Vpra/Chat/Slc18a3tm1.2Vpra *
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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last database update
07/29/2020
MGI 6.15
The Jackson Laboratory