Del(7Ube3a-Snrpn)1Alb Complex/Cluster/Region Detail

Summary

• Symbol
  Del(7Ube3a-Snrpn)1Alb
• Name
  Deletion, Chr 7, Beaudet 1
• Synonyms
  Del1Alb

• Feature Type
  complex/cluster/region
• IDs
  MGI:3655807

Location &
Maps

• Sequence Map
  Chr7:58878498-59789967 bp

  From MGI annotation of GRCm39
  

• View this region in JBrowse
  

• Genome Browsers
  Ensembl | UCSC | NCBI

• Genetic Map
  Chromosome 7, Syntenic

Strain
Comparison

• SNPs within 2kb
  11958 from dbSNP Build 142

Mutations,
Alleles, and
Phenotypes

• Phenotype Summary
  9 phenotypes from 1 allele in 1 genetic background
  7 phenotype references
  

• All Mutations and Alleles
  1
• Targeted
  1
• Find Mice (IMSR)
  0 strains or lines available

References

• Summaries
  All 8

  Phenotypes 7
• Earliest
  J:56617 Tsai TF, et 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
• Latest
  J:254383 Kim Y, et al., Targeting the histone methyltransferase G9a activates imprinted genes and improves survival of a mouse model of Prader-Willi syndrome. Nat Med. 2017 Feb;23(2):213-222