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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
Genes
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)
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04/23/2024
MGI 6.23 		The Jackson Laboratory