Mapping Data Summary

• Symbol: DXMit28
• Name: DNA segment, Chr X, Massachusetts Institute of Technology 28
• ID: MGI:95100
• Chromosome: X

27 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 Mapping Panel: JAX (BSS)	X	J:61762 Buchner G, et al., Identification of a new EGF-repeat-containing gene from human Xp22: a candidate for developmental disorders. Genomics. 2000 Apr 1;65(1):16-23
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
CROSS	Cross Type: Backcross	X	J:31843 Du L, et al., Fine genetic mapping of the Hyp mutation on mouse chromosome X. Genomics. 1996 Mar 1;32(2):177-83
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
CROSS	Cross Type: Backcross	XY	J:32007 Pardo-Manuel de Villena F, et al., Genetic mapping of DXYMov15-associated sequences in the pseudoautosomal region of the C57BL/6J strain. Mamm Genome. 1996 Mar;7(3):237-9
CROSS	Cross Type: Backcross	X	J:19674 Stambolian D, et al., Mapping of the X-linked cataract (Xcat) mutation, the gene implicated in the Nance Horan syndrome, on the mouse X chromosome. Genomics. 1994 Jul 15;22(2):377-80
CROSS	Cross Type: Backcross	X	J:19674 Stambolian D, et al., Mapping of the X-linked cataract (Xcat) mutation, the gene implicated in the Nance Horan syndrome, on the mouse X chromosome. Genomics. 1994 Jul 15;22(2):377-80
CROSS	Cross Type: Backcross Mapping Panel: UCLA (BSB)	X	J:34178 Welch CL, et al., Genetic regulation of cholesterol homeostasis: chromosomal organization of candidate genes. J Lipid Res. 1996 Jul;37(7):1406-21
CROSS	Cross Type: Backcross	X	J:25179 Zhou E, et al., Exclusion of three candidate genes, Grpr, Cxn33, and Pdha1, for the X-linked cataract gene on the distal region of the mouse chromosome X. Mamm Genome. 1995 May;6(5):357-9
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:46280 Blair HJ, et al., An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome. Genomics. 1998 Feb 15;48(1):128-31
TEXT		X	J:46280 Blair HJ, et al., An integrated genetic and man-mouse comparative map of the DXHXS674-Pdha1 region of the mouse X chromosome. Genomics. 1998 Feb 15;48(1):128-31
TEXT-Genetic Cross		X	J:52871 De Plaen E, et al., A new family of mouse genes homologous to the human MAGE genes. Genomics. 1999 Jan 15;55(2):176-84
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-Genetic Cross		X	J:15567 Warden CH, et al., Linkage mapping of 40 randomly isolated liver cDNA clones in the mouse. Genomics. 1993 Nov;18(2):295-307
TEXT-Physical Mapping		X	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-Radiation Hybrid		X	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;