Mapping Data Summary

• Symbol: D8Mit75
• Name: DNA segment, Chr 8, Massachusetts Institute of Technology 75
• ID: MGI:94443
• Chromosome: 8

14 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross Mapping Panel: EUCIB	8	J:48971 Grewal PK, et al., High-resolution mapping of mouse chromosome 8 identifies an evolutionary chromosomal breakpoint. Mamm Genome. 1998 Aug;9(8):603-7
CROSS	Cross Type: Backcross Mapping Panel: EUCIB	8	J:40667 Grewal PK, et al., The mouse homolog of FRG1, a candidate gene for FSHD, maps proximal to the myodystrophy mutation on chromosome 8. Mamm Genome. 1997 Jun;8(6):394-8
CROSS	Cross Type: Backcross	8	J:33549 Kono DH, et al., Jak3 maps to chromosome 8. Mamm Genome. 1996 Jun;7(6):476-7
CROSS	Cross Type: Other	8	J:26061 Mathews KD, et al., Mouse myodystrophy (myd) mutation: refined mapping in an interval flanked by homology with distal human 4q. Muscle Nerve. 1995;Suppl(2):S98-102
CROSS	Cross Type: Backcross	8	J:24378 Mills KA, et al., Genetic mapping near the myd locus on mouse chromosome 8. Mamm Genome. 1995 Apr;6(4):278-80
RI	RI/RC Set: SWXJ	8	J:34480 Shultz KL, et al., Strain distribution pattern for SSLP markers in the SWXJ recombinant inbred strain set: chromosomes 7 to X. Mamm Genome. 1996 Jul;7(7):526-32
RI	RI/RC Set: BXD	8	J:49829 Taylor BA, et al., Genotyping new BXD recombinant inbred mouse strains and comparison of BXD and consensus maps. Mamm Genome. 1999 Apr;10(4):335-48
TEXT		8	J:33012 Campbell DB, et al., Chromosomal localization of the neurological mouse mutations tottering (tg), Purkinje cell degeneration (pcd), and nervous (nr). Brain Res Mol Brain Res. 1996 Apr;37(1-2):79-84
TEXT		8	J:24378 Mills KA, et al., Genetic mapping near the myd locus on mouse chromosome 8. Mamm Genome. 1995 Apr;6(4):278-80
TEXT		8	J:39233 Turker MS, et al., Molecular evidence for the induction of large interstitial deletions on mouse chromosome 8 by ionizing radiation. Mutat Res. 1997 Mar 21;374(2):201-8
TEXT-Genetic Cross		8	J:36596 Fletcher CF, et al., Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell. 1996 Nov 15;87(4):607-17
TEXT-Genetic Cross		8	J:36596 Fletcher CF, et al., Absence epilepsy in tottering mutant mice is associated with calcium channel defects. Cell. 1996 Nov 15;87(4):607-17
TEXT-QTL		8	J:88522 Bouxsein ML, et al., Mapping quantitative trait Loci for vertebral trabecular bone volume fraction and microarchitecture in mice. J Bone Miner Res. 2004 Apr;19(4):587-99
TEXT-QTL		8	J:124160 Jiao Y, et al., Quantitative Trait Loci that Determine Mouse Tibial Nanoindentation Properties in an F(2) Population Derived from C57BL/6J X C3H/HeJ. Calcif Tissue Int. 2007 Jun;80(6):383-90