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Symbol
Name
ID

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

Phenotype annotations related to homeostasis/metabolism

Darker colors indicate more annotations

Human Phenotypes	Exercise intolerance
Disease(s) Associated with SLC18A3	Exercise intolerance
congenital myasthenic syndrome 21

Mouse Phenotypes		impaired exercise endurance	cyanosis	increased acetylcholine level
Availability	Mouse Genotype	impaired exercise endurance	cyanosis	increased acetylcholine level
	Chat/Slc18a3^tm1.1Vpra/Chat/Slc18a3^tm1.1Vpra
	Slc18a3^tm1Mca/Slc18a3^tm1Mca
	Chat/Slc18a3^tm1.1Vpra/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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