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Protein Coding Gene : Slc13a1 solute carrier family 13 (sodium/sulfate symporters), member 1
Primary Identifier  MGI:1859937 Organism  mouse, laboratory
Chromosome  6 NCBI Gene Number  55961
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables sodium:sulfate symporter activity. Acts upstream of or within sulfate transport. Predicted to be located in apical plasma membrane. Predicted to be active in plasma membrane. Is expressed in several structures, including alimentary system; central nervous system; metanephros; musculoskeletal system; and sensory organ. Orthologous to human SLC13A1 (solute carrier family 13 member 1).
PHENOTYPE: Homozygous mutant mice exhibit hyposulfatemia, growth retardation, reduced female fertility, and spontaneous clonic seizures. [provided by MGI curators]
  • synonyms:
  • MGI:2141522,
  • expressed sequence AI314066,
  • solute carrier family 13 (sodium/sulfate symporters), member 1,
  • expressed sequence AI987826,
  • MGI:2141388,
  • Nas1,
  • NaSi-1,
  • AI987826,
  • AI314066,
  • Slc13a1
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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.

Features --> Overlapping features

Proteins

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Mouse features --> Functions (GO terms)

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Interactions

4 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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