Mapping Data Summary

• Symbol: D19Mit89
• Name: DNA segment, Chr 19, Massachusetts Institute of Technology 89
• ID: MGI:100758
• Chromosome: 19

9 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	19	J:48979 Bloom ML, et al., The hemoglobin-deficit mutation is located on mouse chromosome 19. Mamm Genome. 1998 Aug;9(8):666-7
CROSS	Cross Type: Backcross	19	J:51693 Grimm C, et al., Aphakia (ak), a mouse mutation affecting early eye development: fine mapping, consideration of candidate genes and altered Pax6 and Six3 gene expression pattern. Dev Genet. 1998;23(4):299-316
RI	RI/RC Set: BXD	19	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		19	J:45215 McCarthy LC, et al., A first-generation whole genome-radiation hybrid map spanning the mouse genome. Genome Res. 1997 Dec;7(12):1153-61
TEXT-Cytogenetic Localization		19	J:54008 Chi H, et al., Multiple inositol polyphosphate phosphatase: evolution as a distinct group within the histidine phosphatase family and chromosomal localization of the human and mouse genes to chromosomes 10q23 and 19. Genomics. 1999 Mar 15;56(3):324-36
TEXT-Genetic Cross		19	J:42484 Gardner JM, et al., The mouse pale ear (ep) mutation is the homologue of human Hermansky-Pudlak syndrome. Proc Natl Acad Sci U S A. 1997 Aug 19;94(17):9238-43
TEXT-QTL		19	J:85787 Menge DM, et al., Mapping of chromosomal regions influencing immunological responses to gastrointestinal nematode infections in mice. Parasite Immunol. 2003 Jun;25(6):341-9
TEXT-Radiation Hybrid		19	J:57796 Li H, et al., Characterization and expression of sema4g, a novel member of the semaphorin gene family. Mech Dev. 1999 Sep;87(1-2):169-73
TEXT-Radiation Hybrid		19	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;