Mine Disruption Phenotype

Gene Info

  • Species: Mouse (Mus musculus)
  • GeneID: 20512
  • Symbol: Slc1a3
  • Description: solute carrier family 1 (glial high affinity glutamate transporter), member 3
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Gene ID Entry Entry Name Protein Name Type Information
20512 P56564 EAA1_MOUSE Excitatory amino acid transporter 1 (Glial high affinity glutamate transporter) (High-affinity neuronal glutamate transporter) (GluT-1) (Sodium-dependent glutamate/aspartate transporter 1) (GLAST-1) (Solute carrier family 1 member 3) DISRUPTION PHENOTYPE No visible phenotype (PubMed:15363892, PubMed:15390100). Mutant mice display normal locomotion, motor coordination and learning, and globally normal glutamate uptake in brain vesicle preparations (PubMed:15363892). The decay time of glutamate receptor mediated excitatory postsynaptic currents (EPSCs) in cerebellar Purkinje is slightly increased (PubMed:15363892). The decreased rate of glutamate uptake in retina Mueller cells from mutant mice suggests that Slc1a3 accounts for about half of the glutamate uptake activity in wild-type cells (PubMed:15390100). Mice deficient in both Slc1a2 and Slc1a3 die at about 17 dpc (PubMed:16880397). {ECO:0000269|PubMed:15363892, ECO:0000269|PubMed:15390100, ECO:0000269|PubMed:16880397}.