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Protein Coding Gene : Rpl24 ribosomal protein L24
Primary Identifier  MGI:1915443 Organism  mouse, laboratory
Chromosome  16 NCBI Gene Number  68193
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

A structural constituent of ribosome. Acts upstream of or within several processes, including exit from mitosis; nervous system development; and retina development in camera-type eye. Located in cytoplasm. Part of cytosolic large ribosomal subunit. Is active in synapse. Is expressed in embryo; metanephros; spleen; and thymus. Used to study optic atrophy. Orthologous to human RPL24 (ribosomal protein L24).
PHENOTYPE: Heterozygous mutants have short kinked tail, ventral spotting, malocclusion, white feet, and anomalies of the spine and eyes; homozygotes die in utero. [provided by MGI curators]
  • synonyms:
  • 0610008L05Rik,
  • belly spot and tail,
  • Rpl24,
  • ribosomal protein L24,
  • RIKEN cDNA 0610008L05 gene,
  • MGD-MRK-1677,
  • Bst,
  • MGI:88211
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Features --> Cross References

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Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

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Canonical gene --> Transcripts in specific strains.

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Proteins

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Interactions

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Gene --> Protein-Protein Interactions

Expression

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Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

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Literature

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