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Protein Coding Gene : Slc22a12 solute carrier family 22 (organic anion/cation transporter), member 12
Primary Identifier  MGI:1195269 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  20521
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables urate transmembrane transporter activity. Acts upstream of or within urate transport. Located in brush border membrane. Is expressed in central nervous system; dorsal root ganglion; male reproductive gland or organ; metanephros; and retina layer. Orthologous to human SLC22A12 (solute carrier family 22 member 12).
PHENOTYPE: Mice homozygous for a null allele exhibit increased urinary urate levels and altered urine and plasma metabolite composition. [provided by MGI curators]
  • synonyms:
  • MGI:2147622,
  • solute carrier family 22 (organic anion/cation transporter), member 12,
  • AI987855,
  • Rst,
  • URAT1,
  • Slc22a12,
  • Slc22al2,
  • expressed sequence AI987855,
  • solute carrier family 22 (organic cation transporter)-like 2
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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

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5 Pathways

Trail: ProteinCodingGene

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Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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