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Symbol
Name
ID
Slc18a3
solute carrier family 18 (vesicular monoamine), member 3
MGI:1101061
Phenotype annotations related to muscle
Darker colors indicate more annotations
Human Phenotypes
Knee flexion contracture
Facial palsy
Generalized hypotonia
Difficulty walking
Exercise intolerance
Disease(s) Associated with SLC18A3
congenital myasthenic syndrome 21

Mouse Phenotypes
skeletal muscle fiber atrophy
abnormal skeletal muscle morphology
skeletal muscle atrophy
hypotonia
Availability Mouse Genotype
Chat/Slc18a3tm1.1Vpra/Chat/Slc18a3tm1.1Vpra

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
08/04/2020
MGI 6.15
The Jackson Laboratory