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Symbol
Name
ID
Slc1a1
solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
MGI:105083
Phenotype annotations related to nervous system
Darker colors indicate more annotations
Human Phenotypes
Intellectual disability
Disease(s) Associated with SLC1A1
dicarboxylic aminoaciduria

Mouse Phenotypes
decreased retinal ganglion cell number
optic nerve degeneration
Availability Mouse Genotype
Slc1a1tm1Wst/Slc1a1tm1Wst

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
06/18/2019
MGI 6.14
The Jackson Laboratory