About   Help   FAQ
Mapping Data
Experiment
  • Experiment
    TEXT
  • Chromosome
    11
  • Reference
    J:125240 Yan J, et al., Penetrance of craniofacial anomalies in mouse models of Smith-Magenis syndrome is modified by genomic sequence surrounding Rai1: not all null alleles are alike. Am J Hum Genet. 2007 Mar;80(3):518-25
  • ID
    MGI:3765155
Notes
  • Experiment
    The loci were ordered as listed here in mouse Chromosome 11 and were inclusive in overlapping deletions Del(11Cops3-4933439F18Rik)2Jrl, Del(11Cops3-4933439F18Rik)3Jrl and Del(11Cops3-4933439F18Rik)4Jrl. The nested deletions were included within approximately 2 Mbs of DNA. The largest deleted region included the loci from Cops3 to Zfp179. All deletions covered the Rai1 locus.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
12/10/2024
MGI 6.24
The Jackson Laboratory