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Protein Coding Gene : Slc23a2 solute carrier family 23 (nucleobase transporters), member 2
Primary Identifier  MGI:1859682 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  54338
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

Enables L-ascorbate:sodium symporter activity and L-ascorbic acid transmembrane transporter activity. Involved in L-ascorbic acid transmembrane transport. Acts upstream of or within blood circulation. Located in basal plasma membrane and cytoplasm. Is expressed in adrenal gland; central nervous system; liver; metanephros; and retina. Orthologous to human SLC23A2 (solute carrier family 23 member 2).
PHENOTYPE: Mice homozygous for disruptions in this gene die within minutes of birth from respiratory distress. [provided by MGI curators]
  • synonyms:
  • Slc23a1,
  • Slc23a2,
  • AI844736,
  • SVCT2,
  • solute carrier family 23 (nucleobase transporters), member 1,
  • MGI:2139069,
  • mKIAA0238,
  • Slco1a1,
  • solute carrier family 23 (nucleobase transporters), member 2,
  • expressed sequence AI844736,
  • YSPL3
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Features --> Cross References

Genome

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0 Canonical

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2 Involved In Mutations

Trail: ProteinCodingGene

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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

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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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