Mapping Data Summary

• Symbol: D3Mit6
• Name: DNA segment, Chr 3, Massachusetts Institute of Technology 6
• ID: MGI:92530
• Chromosome: 3

16 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Intercross	3	J:53340 Sprunger LK, et al., Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3. Hum Mol Genet. 1999 Mar;8(3):471-9
RI	RI/RC Set: AKXL	3	J:17312 Cheah YC, et al., Strain distribution patterns for 50 SSLP markers in the murine AKXL recombinant inbred set. Mamm Genome. 1994 Mar;5(3):189-90
RI	RI/RC Set: BXA	3	J:3521 Mu JL, et al., Strain distribution pattern of 25 simple sequence length polymorphisms in the AXB and BXA recombinant inbred strains. Mamm Genome. 1992;3(12):705-8
RI	RI/RC Set: AXB	3	J:3521 Mu JL, et al., Strain distribution pattern of 25 simple sequence length polymorphisms in the AXB and BXA recombinant inbred strains. Mamm Genome. 1992;3(12):705-8
RI	RI/RC Set: CXB	3	J:39615 Panoutsakopoulou V, et al., Microsatellite typing of CXB recombinant inbred and parental mouse strains. Mamm Genome. 1997 May;8(5):357-61
RI	RI/RC Set: OcB	3	J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8
RI	RI/RC Set: HcB(N3)	3	J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8
RI	RI/RC Set: HcB(N4)	3	J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8
RI	RI/RC Set: BXD	3	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-Genetic Cross		3	J:22965 Li Y, et al., A fibrillar collagen gene, Col11a1, is essential for skeletal morphogenesis [see comments]. Cell. 1995 Feb 10;80(3):423-30
TEXT-Genetic Cross		3	J:53340 Sprunger LK, et al., Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3. Hum Mol Genet. 1999 Mar;8(3):471-9
TEXT-Physical Mapping		3	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-QTL		3	J:67840 Butterfield RJ, et al., Identification of genetic loci controlling the characteristics and severity of brain and spinal cord lesions in experimental allergic encephalomyelitis. Am J Pathol. 2000 Aug;157(2):637-45
TEXT-QTL		3	J:98123 Geiger H, et al., Age- and stage-specific regulation patterns in the hematopoietic stem cell hierarchy. Blood. 2001 Nov 15;98(10):2966-72
TEXT-QTL		3	J:53794 Le Roy I, et al., Preweanling sensorial and motor development in laboratory mice: quantitative trait loci mapping. Dev Psychobiol. 1999 Mar;34(2):139-58
TEXT-QTL		3	J:31314 Teuscher C, et al., Aod2, the locus controlling development of atrophy in neonatal thymectomy-induced autoimmune ovarian dysgenesis, co-localizes with Il2, Fgfb, and Idd3. J Exp Med. 1996 Feb 1;183(2):631-7