Mapping Data Summary

• Symbol: Magel2
• Name: MAGE family member L2
• ID: MGI:1351648
• Chromosome: 7

6 mapping experiments

Experiment Type	Details	Chromosome	Reference
TEXT		7	J:72512 Choi JD, et al., Microarray expression profiling of tissues from mice with uniparental duplications of Chromosomes 7 and 11 to identify imprinted genes. Mamm Genome. 2001 Oct;12(10):758-64
TEXT-Physical Mapping		7	J:58785 Boccaccio I, et al., The human MAGEL2 gene and its mouse homologue are paternally expressed and mapped to the Prader-Willi region. Hum Mol Genet. 1999 Dec;8(13):2497-505
TEXT-Physical Mapping		7	J:72417 Chai JH, et al., Retrotransposed genes such as Frat3 in the mouse Chromosome 7C Prader-Willi syndrome region acquire the imprinted status of their insertion site. Mamm Genome. 2001 Nov;12(11):813-21
TEXT-Physical Mapping		7	J:63703 Lee S, et al., Expression and imprinting of MAGEL2 suggest a role in Prader-willi syndrome and the homologous murine imprinting phenotype. Hum Mol Genet. 2000 Jul 22;9(12):1813-9
TEXT-Physical Mapping		7	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-Physical Mapping		7	J:101829 Watrin F, et al., The Prader-Willi syndrome murine imprinting center is not involved in the spatio-temporal transcriptional regulation of the Necdin gene. BMC Genet. 2005 Jan 5;6(1):1