Mapping Data Summary

• Symbol: D13Mit265
• Name: DNA segment, Chr 13, Massachusetts Institute of Technology 265
• ID: MGI:101070
• Chromosome: 13

6 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Intercross	13	J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
TEXT		13	J:51890 Cox GA, et al., Identification of the mouse neuromuscular degeneration gene and mapping of a second site suppressor allele. Neuron. 1998 Dec;21(6):1327-37
TEXT-Genetic Cross		13	J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
TEXT-Physical Mapping		13	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-Radiation Hybrid		13	J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
TEXT-Radiation Hybrid		13	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;