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Symbol
Name
ID
Slc19a3
solute carrier family 19, member 3
MGI:1931307
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Fever
Disease(s) Associated with SLC19A3
biotin-responsive basal ganglia disease

Mouse Phenotypes
abnormal vitamin absorption
abnormal thiamin level
Availability Mouse Genotype
Slc19a3tm1.1Nwak/Slc19a3tm1.1Nwak
Slc19a3tm1Said/Slc19a3tm1Said

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
10/08/2019
MGI 6.14
The Jackson Laboratory