About   Help   FAQ
Symbol
Name
ID
Slc38a3
solute carrier family 38, member 3
MGI:1923507
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Atypical behavior
Disease(s) Associated with SLC38A3
developmental and epileptic encephalopathy 102

Mouse Phenotypes
lethargy
ataxia
Availability Mouse Genotype
Slc38a3m1Ingm/Slc38a3m1Ingm

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/16/2024
MGI 6.23
The Jackson Laboratory