Mapping Data Summary

• Symbol: D5Mit338
• Name: DNA segment, Chr 5, Massachusetts Institute of Technology 338
• ID: MGI:100378
• Chromosome: 5

17 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	5	J:40511 Agui T, et al., Mapping of the grt locus to mouse Chromosome 5. Mamm Genome. 1997 Dec;8(12):944
CROSS	Cross Type: Backcross	5	J:38358 Bussoli TJ, et al., Localization of the bronx waltzer (bv) deafness gene to mouse chromosome 5. Mamm Genome. 1997 Oct;8(10):714-7
CROSS	Cross Type: Backcross	5	J:38358 Bussoli TJ, et al., Localization of the bronx waltzer (bv) deafness gene to mouse chromosome 5. Mamm Genome. 1997 Oct;8(10):714-7
RI	RI/RC Set: EXCB	5	J:121994 Grzmil P, et al., STS markers on chromosome 1, 3, 5, 8 and 9 in CBXE and EXCB recombinant inbred strains of mice. MGI Direct Data Submission. 2007;
RI	RI/RC Set: CBXE	5	J:121994 Grzmil P, et al., STS markers on chromosome 1, 3, 5, 8 and 9 in CBXE and EXCB recombinant inbred strains of mice. MGI Direct Data Submission. 2007;
TEXT		5	J:80013 Joober R, et al., Provisional mapping of quantitative trait Loci modulating the acoustic startle response and prepulse inhibition of acoustic startle. Neuropsychopharmacology. 2002 Nov;27(5):765-81
TEXT-Congenic		5	J:203042 Hoover-Plow J, et al., Genetic dissection of quantitative trait Loci for hemostasis and thrombosis on mouse chromosomes 11 and 5 using congenic and subcongenic strains. PLoS One. 2013;8(10):e77539
TEXT-Genetic Cross		5	J:39922 British Society of Audiology short papers meeting on experimental studies of hearing and deafness. Cambridge, United Kingdom, 22-23 September 1996. Bussoli T, et al., Localization of the bronx waltzer mouse mutation and its effect on organ of Corti development. Br J Audiol. 1997 Apr;31(2):73-132 (83 Abstr.)
TEXT-Genetic Cross		5	J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003;
TEXT-Genetic Cross		5	J:92463 JAX Reproductive Mutagenesis Program, Heritable mouse mutants from The Jackson Laboratory Reproductive Genomics Mutagenesis Program. MGI Direct Data Submission. 2004-7;
TEXT-Genetic Cross		5	J:75144 Suzuki T, et al., Hermansky-Pudlak syndrome is caused by mutations in HPS4, the human homolog of the mouse light-ear gene. Nat Genet. 2002 Mar;30(3):321-4
TEXT-Physical Mapping		5	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-QTL		5	J:68879 Boyartchuk VL, et al., Multigenic control of Listeria monocytogenes susceptibility in mice. Nat Genet. 2001 Mar;27(3):259-60
TEXT-QTL		5	J:142950 Dietz JA, et al., Rgcs1, a dominant QTL that affects retinal ganglion cell death after optic nerve crush in mice. BMC Neurosci. 2008;9:74
TEXT-QTL		5	J:184231 Jiao Y, et al., Genetic dissection of strain dependent paraquat-induced neurodegeneration in the substantia nigra pars compacta. PLoS One. 2012;7(1):e29447
TEXT-QTL		5	J:139651 Sa Q, et al., Quantitative trait locus analysis for hemostasis and thrombosis. Mamm Genome. 2008 Jun;19(6):406-12
TEXT-Radiation Hybrid		5	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;