Mapping Data Summary

• Symbol: Smcr8
• Name: Smith-Magenis syndrome chromosome region, candidate 8 homolog (human)
• ID: MGI:2444720
• Chromosome: 11

3 mapping experiments

Experiment Type	Details	Chromosome	Reference
TEXT		11	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
TEXT-Physical Mapping		11	J:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
TEXT-Radiation Hybrid		11	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;