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Protein Coding Gene : Snrnp200 small nuclear ribonucleoprotein 200 (U5)
Primary Identifier  MGI:2444401 Organism  mouse, laboratory
Chromosome  2 NCBI Gene Number  320632
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Predicted to enable RNA helicase activity and identical protein binding activity. Predicted to be involved in spliceosome conformational change to release U4 (or U4atac) and U1 (or U11). Predicted to act upstream of or within RNA splicing and mRNA processing. Predicted to be located in nucleoplasm. Predicted to be part of spliceosomal complex and spliceosomal snRNP complex. Is expressed in several structures, including cardiovascular system; central nervous system; genitourinary system; gut; and sensory organ. Human ortholog(s) of this gene implicated in retinitis pigmentosa and retinitis pigmentosa 33. Orthologous to human SNRNP200 (small nuclear ribonucleoprotein U5 subunit 200).
PHENOTYPE: Mice homozygous for a transgenic gene disruption exhibit embryonic lethality before implantation. [provided by MGI curators]
  • synonyms:
  • U5-200KD,
  • small nuclear ribonucleoprotein 200 (U5),
  • MGI:2679724,
  • HELIC2,
  • BC011390,
  • activating signal cointegrator 1 complex subunit 3-like 1,
  • cDNA sequence BC011390,
  • RIKEN cDNA A330064G03 gene,
  • Ascc3l1,
  • Snrnp200,
  • A330064G03Rik
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