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Protein Coding Gene : Slc31a2 solute carrier family 31, member 2

Primary Identifier  MGI:1333844 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  20530
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable copper ion transmembrane transporter activity. Acts upstream of or within intracellular copper ion homeostasis and regulation of copper ion transmembrane transport. Located in late endosome; membrane; and recycling endosome. Is expressed in brain; retina nuclear layer; and urinary system. Orthologous to human SLC31A2 (solute carrier family 31 member 2).
PHENOTYPE: Mice homozygous for a null allele display copper accumulation in the brain, kidney, spleen, muscle and testes but not in the liver. [provided by MGI curators]
  • synonyms:
  • MGI:2140341,
  • expressed sequence AI604396,
  • solute carrier family 31, member 2,
  • Slc31a2,
  • Ctr2,
  • AI604396

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

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0 Involved In Mutations

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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

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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