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Protein Coding Gene : Slc7a10 solute carrier family 7 (cationic amino acid transporter, y+ system), member 10
Primary Identifier  MGI:1858261 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  53896
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables neutral L-amino acid transmembrane transporter activity. Involved in negative regulation of brown fat cell differentiation; neutral amino acid transport; and positive regulation of glycinergic synaptic transmission. Acts upstream of or within D-alanine transmembrane transport. Located in plasma membrane. Is expressed in brain; embryo mesenchyme; naris; and spinal cord ventricular layer. Orthologous to human SLC7A10 (solute carrier family 7 member 10).
PHENOTYPE: A targeted mutation of this gene results in mice that develop tremors, ataxia and seizures. [provided by MGI curators]
  • synonyms:
  • MGI:2142097,
  • expressed sequence AL024237,
  • Slc7a10,
  • solute carrier family 7 (cationic amino acid transporter, y+ system), member 10,
  • AL024237,
  • Asc-1,
  • D7Bwg0847e,
  • DNA segment, Chr 7, Brigham & Women's Genetics 0847 expressed,
  • MGD-MRK-34148,
  • MGI:106454
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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.

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7 Pathways

Trail: ProteinCodingGene

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Phenotype

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Disease

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