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Protein Coding Gene : Slc1a6 solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6
Primary Identifier  MGI:1096331 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  20513
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables L-glutamate transmembrane transporter activity. Acts upstream of or within L-glutamate transmembrane transport; establishment of localization in cell; and regulation of membrane potential. Located in Golgi apparatus and membrane. Is active in glutamatergic synapse and presynaptic membrane. Is expressed in central nervous system and retina. Orthologous to human SLC1A6 (solute carrier family 1 member 6).
PHENOTYPE: Mice homozygous for disruptions in this gene survive well and display no obvious abnormalities of behavior or brain structure. [provided by MGI curators]
  • synonyms:
  • solute carrier family 1 (high affinity aspartate/glutamate transporter), member 6,
  • EAAT4,
  • Slc1a6
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Features --> Cross References

Genome

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

Trail: ProteinCodingGene

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

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Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

7 Pathways

Trail: ProteinCodingGene

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Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

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1 Driver For

Trail: ProteinCodingGene




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