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Protein Coding Gene : Cwc27 CWC27 spliceosome-associated protein
Primary Identifier  MGI:1914535 Organism  mouse, laboratory
Chromosome  13 NCBI Gene Number  67285
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable peptidyl-prolyl cis-trans isomerase activity. Predicted to be involved in protein folding. Located in nucleus. Is expressed in alimentary system; brain; genitourinary system; and trachea. Used to study retinitis pigmentosa. Orthologous to human CWC27 (CWC27 spliceosome associated cyclophilin).
PHENOTYPE: Homozygous mutant mice exhibit reduced viability. Surviors after birth show signs of growth retardation and retinal depigmentation, along with numerous neurological, immunological, and blood chemistry abnormalities. [provided by MGI curators]
  • synonyms:
  • NY-CO-10,
  • Cwc27,
  • RIKEN cDNA 3110009E13 gene,
  • Sdccag10,
  • CWC27 spliceosome-associated protein,
  • 3110009E13Rik,
  • serologically defined colon cancer antigen 10
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