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Protein Coding Gene : Nsun5 NOL1/NOP2/Sun domain family, member 5

Primary Identifier  MGI:2140844 Organism  mouse, laboratory
Chromosome  5 NCBI Gene Number  100609
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Enables rRNA (cytosine-C5-)-methyltransferase activity. Involved in several processes, including central nervous system development; rRNA base methylation; and regulation of myelination. Predicted to be located in nucleoplasm. Predicted to be active in nucleolus. Is expressed in several structures, including alimentary system; branchial arch; central nervous system; genitourinary system; and sensory organ. Orthologous to several human genes including NSUN5 (NOP2/Sun RNA methyltransferase 5).
PHENOTYPE: Mice homozygous for a knock-out allele exhibit impaired spatial working memory and learning with decreased LTP and reduced OPC proliferation. [provided by MGI curators]
  • synonyms:
  • Williams Beuren syndrome chromosome region 20A homolog (human),
  • expressed sequence AI326939,
  • Nsun5,
  • NOL1/NOP2/Sun domain family, member 5,
  • Nol1r,
  • RIKEN cDNA 9830109N13 gene,
  • MGI:2157794,
  • Wbscr20a,
  • 9830109N13Rik,
  • AI326939

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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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