Mapping Data Summary

• Symbol: Wrn
• Name: Werner syndrome RecQ like helicase
• ID: MGI:109635
• Chromosome: 8

8 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	8	J:66161 Dron M, et al., Mouse scrapie responsive gene 1 (Scrg1): genomic organization, physical linkage to sap30, genetic mapping on chromosome 8, and expression in neuronal primary cell cultures. Genomics. 2000 Nov 15;70(1):140-9
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	8	J:48424 Lebel M, et al., A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity. Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13097-102
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSB)	8	J:48424 Lebel M, et al., A deletion within the murine Werner syndrome helicase induces sensitivity to inhibitors of topoisomerase and loss of cellular proliferative capacity. Proc Natl Acad Sci U S A. 1998 Oct 27;95(22):13097-102
FISH	Band: A4	8	J:39875 Imamura O, et al., Cloning of a mouse homologue of the human Werner syndrome gene and assignment to 8A4 by fluorescence in situ hybridization. Genomics. 1997 Apr 15;41(2):298-300
FISH	Band: A3	8	J:48529 Wu J, et al., Effect of age and apoptosis on the mouse homologue of the huWRN gene. Mech Ageing Dev. 1998 Jun 1;103(1):27-44
TEXT-Physical Mapping		8	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-QTL		8	J:112037 Sebastiani G, et al., Mapping genetic modulators of amyloid plaque deposition in TgCRND8 transgenic mice. Hum Mol Genet. 2006 Aug 1;15(15):2313-23
TEXT-Radiation Hybrid		8	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;