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Symbol
Name
ID

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

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Knee flexion contracture
Disease(s) Associated with SLC18A3	Knee flexion contracture
congenital myasthenic syndrome 21

Mouse Phenotypes		kyphosis
Availability	Mouse Genotype	kyphosis
	Chat/Slc18a3^tm1.1Vpra/Chat/Slc18a3^tm1.1Vpra

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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