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Symbol
Name
ID

Slc19a3
solute carrier family 19, member 3
MGI:1931307

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Lethargy
Disease(s) Associated with SLC19A3	Lethargy
biotin-responsive basal ganglia disease

Mouse Phenotypes		lethargy	abnormal locomotor behavior	paralysis
Availability	Mouse Genotype	lethargy	abnormal locomotor behavior	paralysis
	Slc19a3^tm1.1Nwak/Slc19a3^tm1.1Nwak
	Slc19a3^tm1Said/Slc19a3^tm1Said

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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