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Slc1a3 Gene Detail
Summary
  • Symbol
    Slc1a3
  • Name
    solute carrier family 1 (glial high affinity glutamate transporter), member 3
  • Synonyms
    B430115D02Rik, Eaat1, GLAST, Gmt1, MGluT1
  • Feature Type
    protein coding gene
  • IDs
    MGI:99917
    NCBI Gene: 20512
  • Alliance
    gene page
Location & Maps
more
  • Sequence Map
    Chr15:8634124-8710764 bp, - strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser
  • Download
    Sequence
      76641 bp   ±  kb flank

  • Genome Browsers
    VEGA | Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 15, 3.82 cM, cytoband A2
  • Mapping Data
    8 experiments
Homology
more
  • Human Ortholog
    SLC1A3, solute carrier family 1 member 3
  • Vertebrate Orthologs
    11
  • Human Ortholog
    SLC1A3, solute carrier family 1 member 3
    Orthology source: HomoloGene, HGNC
  • Synonyms
    EA6, EAAT1, GLAST, GLAST1
  • Links
    NCBI Gene ID: 6507
    neXtProt AC: NX_P43003
    UniProt: P43003

  • Chr Location
    5p13.2; chr5:36606355-36688334 (+)  GRCh38.p7
Human Diseases
more
  • Diseases
    1 with Slc1a3 mouse models; 1 with human SLC1A3 associations

Human Disease Mouse Models
      
IDs
 View 1 model
      
IDs
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    2 with disease annotations
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    28 phenotypes from 3 alleles in 4 genetic backgrounds
    10 phenotypes from multigenic genotypes
    87 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mice homozygous for disruptions in this gene display no abnormalities with respect to appearance or survival but do display functional abnormalities related to the central nervous system.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
    66
  • GO References
    20
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
receptor binding
RNA binding
transcription
transferase
transporter
Biological Process

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
synapse
vacuole
Click cells to view annotations.
Expression
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Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    483
  • Tissues
    217
  • cDNA Data
    25
  • Literature Summary
    131
Interactions
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Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000032639 VEGA Gene Model | MGI Sequence Detail 76641 C57BL/6J ±  kb
transcript OTTMUST00000081197 VEGA | MGI Sequence Detail 4163 Not Applicable  
polypeptide OTTMUSP00000043391 VEGA | MGI Sequence Detail 543 Not Applicable  
For the selected sequence
Polymorphisms
less
  • SNPs within 2kb
    291 from dbSNP Build 142
  • RFLP
    1
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 37
    Genomic 6
    cDNA 26
    Primer pair 4
    Other 1

    Microarray probesets 9
Other
Accession IDs
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MGD-MRK-16014, MGD-MRK-16274, MGD-MRK-16718, MGI:2146029, MGI:2444735
References
more
  • Summaries
    All 271
    Developmental Gene Expression 131
    Diseases 2
    Gene Ontology 20
    Phenotypes 87
  • Earliest
    J:16962 Tanaka K, Cloning and expression of a glutamate transporter from mouse brain. Neurosci Lett. 1993 Sep 3;159(1-2):183-6
  • Latest
    J:259671 Sun B, et al., Polycomb Protein Eed is Required for Neurogenesis and Cortical Injury Activation in the Subventricular Zone. Cereb Cortex. 2018 Apr 1;28(4):1369-1382
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
04/17/2018
MGI 6.11 		The Jackson Laboratory