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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Slc1a1
solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1
MGI:105083
10 phenotypes from 2 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Slc1a1tm1b(KOMP)Wtsi/Slc1a1tm1b(KOMP)Wtsi
C57BL/6N-Slc1a1tm1b(KOMP)Wtsi/J
decreased total body fat amount J:211773
increased circulating iron level J:211773
Slc1a1tm1Wst/Slc1a1tm1Wst
B6.129-Slc1a1tm1Wst
decreased retinal ganglion cell number J:124191
increased cellular sensitivity to hydrogen peroxide J:124191
increased lactate dehydrogenase level J:124191
optic nerve degeneration J:124191
normal vision/eye phenotype J:124191
Slc1a1tm1Wst/Slc1a1tm1Wst
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
normal behavior/neurological phenotype J:41613
dicarboxylic aciduria J:41613
hypoactivity J:41613

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