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Protein Coding Gene : Rpl10 ribosomal protein L10
Primary Identifier  MGI:105943 Organism  mouse, laboratory
Chromosome  X NCBI Gene Number  110954
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.0.0)

A structural constituent of ribosome. Predicted to be involved in embryonic brain development; negative regulation of apoptotic process; and regulation of gene expression. Predicted to act upstream of or within translation. Located in cytoplasm. Part of cytosolic large ribosomal subunit. Is active in synapse. Colocalizes with smooth endoplasmic reticulum. Is expressed in several structures, including limb; nervous system; otocyst; skin; and surface ectoderm. Human ortholog(s) of this gene implicated in autistic disorder and syndromic X-linked mental retardation 35. Orthologous to human RPL10 (ribosomal protein L10).
  • synonyms:
  • DNA segment, Chr X, human DXS648E,
  • Rpl10,
  • DXHXS648E,
  • MGD-MRK-39623,
  • DXHXS648,
  • MGD-MRK-39622,
  • 24.6kDa protein,
  • ribosomal protein L10,
  • MGI:109624,
  • MGI:109623,
  • DNA segment, Chr X, human DXS648,
  • MGI:88630,
  • MGD-MRK-2369,
  • QM16,
  • MGD-MRK-33622,
  • DNA segment, human DXS648,
  • D0HXS648
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Canonical gene --> Exons in specific strains

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Expression

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Disease

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