Mapping Data Summary

• Symbol: Ndn
• Name: necdin, MAGE family member
• ID: MGI:97290
• Chromosome: 7

15 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	7	J:65556 de Los Santos T, et al., Small evolutionarily conserved RNA, resembling C/D box small nucleolar RNA, is transcribed from PWCR1, a novel imprinted gene in the prader-willi deletion region, which Is highly expressed in brain. Am J Hum Genet. 2000 Nov;67(5):1067-82
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	7	J:47259 Goodwin N, et al., An embryonic stem cell bank for producing deletion complexes in mice. MGI Direct Data Submission. 1998;
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	7	J:43448 MacDonald HR, et al., The necdin gene is deleted in Prader-Willi syndrome and is imprinted in human and mouse. Hum Mol Genet. 1997 Oct;6(11):1873-8
FISH	Band: C	7	J:44959 Watrin F, et al., The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region. Eur J Hum Genet. 1997 Sep-Oct;5(5):324-32
IN SITU	Band: B5-D1	7	J:44959 Watrin F, et al., The mouse Necdin gene is expressed from the paternal allele only and lies in the 7C region of the mouse chromosome 7, a region of conserved synteny to the human Prader-Willi syndrome region. Eur J Hum Genet. 1997 Sep-Oct;5(5):324-32
TEXT		7	J:99883 Buettner VL, et al., Novel paternally expressed intergenic transcripts at the mouse Prader-Willi/Angelman Syndrome locus. Mamm Genome. 2005 Apr;16(4):219-27
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-Congenic		7	J:237465 Cheverud JM, et al., Fine-mapping quantitative trait loci affecting murine external ear tissue regeneration in the LG/J by SM/J advanced intercross line. Heredity (Edinb). 2014 May;112(5):508-18
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
TEXT-QTL		7	J:84615 Krass KL, et al., Genetic loci contributing to age-related hippocampal lesions in mice. Neurobiol Dis. 2003 Jul;13(2):102-8
TEXT-Radiation Hybrid		7	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;