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Protein Coding Gene : Slc1a4 solute carrier family 1 (glutamate/neutral amino acid transporter), member 4
Primary Identifier  MGI:2135601 Organism  mouse, laboratory
Chromosome  11 NCBI Gene Number  55963
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables L-aspartate transmembrane transporter activity; L-serine transmembrane transporter activity; and neutral L-amino acid transmembrane transporter activity. Involved in L-aspartate import across plasma membrane. Acts upstream of or within serine import across plasma membrane. Located in intermediate filament. Is expressed in several structures, including central nervous system; dorsal root ganglion; lung; nose; and thymus primordium. Used to study spastic tetraplegia, thin corpus callosum, and progressive microcephaly. Human ortholog(s) of this gene implicated in spastic tetraplegia, thin corpus callosum, and progressive microcephaly. Orthologous to human SLC1A4 (solute carrier family 1 member 4).
  • synonyms:
  • MGI:2144477,
  • solute carrier family 1 (glutamate/neutral amino acid transporter), member 4,
  • expressed sequence AW045657,
  • AW045657,
  • ASCT1,
  • Slc1a4
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

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

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

4 Pathways

Trail: ProteinCodingGene

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

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0 Driver For





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