Mapping Data Summary

• Symbol: Fbn2
• Name: fibrillin 2
• ID: MGI:95490
• Chromosome: 18

7 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	18	J:21512 Goldstein C, et al., Of mice and Marfan: genetic linkage analyses of the fibrillin genes, Fbn1 and Fbn2, in the mouse genome. Mamm Genome. 1994 Nov;5(11):696-700
FISH	Band: D-E1	18	J:16152 Li X, et al., Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18. Genomics. 1993 Dec;18(3):667-72
HYBRID		18	J:16152 Li X, et al., Fibrillin genes map to regions of conserved mouse/human synteny on mouse chromosomes 2 and 18. Genomics. 1993 Dec;18(3):667-72
TEXT-Genetic Cross		18	J:56631 Dixon MJ, et al., Mutation of the Na-K-Cl co-transporter gene Slc12a2 results in deafness in mice. Hum Mol Genet. 1999 Aug;8(8):1579-84
TEXT-Physical Mapping		18	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		18	J:201479 Srivastava U, et al., Differences in health status affect susceptibility and mapping of genetic loci for atherosclerosis (fatty streak) in inbred mice. Arterioscler Thromb Vasc Biol. 2012 Oct;32(10):2380-6
TEXT-Radiation Hybrid		18	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;