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Protein Coding Gene : Slc24a2 solute carrier family 24 (sodium/potassium/calcium exchanger), member 2
Primary Identifier  MGI:1923626 Organism  mouse, laboratory
Chromosome  4 NCBI Gene Number  76376
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables calcium channel activity. Acts upstream of or within several processes, including learning or memory; neuron cellular homeostasis; and regulation of synaptic plasticity. Located in membrane. Is active in postsynapse and presynapse. Is expressed in lens; lens epithelium; and lens fiber. Orthologous to human SLC24A2 (solute carrier family 24 member 2).
PHENOTYPE: Homozygous mutation of this gene results in loss of long term potentiation and an increase in long term depression and deficits in motor learning and spatial working memory. [provided by MGI curators]
  • synonyms:
  • MGI:1917990,
  • 2810021B17Rik,
  • expressed sequence AI847460,
  • RIKEN cDNA 2810021B17 gene,
  • 6330417K15Rik,
  • AI847460,
  • RIKEN cDNA 6330417K15 gene,
  • Slc24a2,
  • MGI:2140377,
  • solute carrier family 24 (sodium/potassium/calcium exchanger), member 2
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Features --> Cross References

Genome

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5 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

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