Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  7
• Reference
  J:69578 Chamberlain SJ, et al., The prader-willi syndrome imprinting center activates the paternally expressed murine ube3a antisense transcript but represses paternal ube3a. Genomics. 2001 May 1;73(3):316-22
• ID
  MGI:2135660

Genes

Gene	Assay Type
Ube3a	reported elsewhere
Snrpn	reported elsewhere

Notes

• Experiment
  The authors indicated that Ube3a and Snrpn were separated by 500-700 kb on mouse Chromosome 7. The following was used as a mapping reference; J:56617, Tsai TF; Jiang YH; Bressler J; Armstrong D; Beaudet AL, Paternal deletion from Snrpn to Ube3a in the mouse causes hypotonia, growth retardation and partial lethality and provides evidence for a gene contributing to Prader-Willi syndrome., Hum Mol Genet 1999 Aug;8(8):1357-64.