Mapping Data Summary

• Symbol: DXMit21
• Name: DNA segment, Chr X, Massachusetts Institute of Technology 21
• ID: MGI:95093
• Chromosome: X

13 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
CROSS	Cross Type: Backcross	X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
CROSS	Cross Type: Backcross	X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
CROSS	Cross Type: Backcross	X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
CROSS	Cross Type: Backcross	X	J:52809 Gormally E, et al., Faint lined (Fnl): a novel X-linked coat mutant in the mouse. Genet Res. 1998 Dec;72(3):211-6
TEXT		X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
TEXT		X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
TEXT		X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
TEXT		X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
TEXT		X	J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
TEXT		X	J:63141 Weber HC, et al., Molecular organization of the mouse gastrin-releasing peptide receptor gene and its promoter. Gene. 2000 Feb 22;244(1-2):137-49
TEXT-Genetic Cross		X	J:52809 Gormally E, et al., Faint lined (Fnl): a novel X-linked coat mutant in the mouse. Genet Res. 1998 Dec;72(3):211-6
TEXT-Physical Mapping		X	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;