Mapping Data Summary

• Symbol: D19Mit101
• Name: DNA segment, Chr 19, Massachusetts Institute of Technology 101
• ID: MGI:100778
• Chromosome: 19

8 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:105712 White RA, et al., Iron metabolism mutant hbd mice have a deletion in Sec15l1, which has homology to a yeast gene for vesicle docking. Genomics. 2005 Dec;86(6):668-73
TEXT-Genetic Cross		19	J:105022 Lim JE, et al., A mutation in Sec15l1 causes anemia in hemoglobin deficit (hbd) mice. Nat Genet. 2005 Nov;37(11):1270-3
TEXT-Genetic Cross		19	J:63778 Simon-Chazottes D, et al., Genomic organization, chromosomal assignment, and expression analysis of the mouse suppressor of fused gene (Sufu) coding a Gli protein partner. Mamm Genome. 2000 Aug;11(8):614-21
TEXT-Physical Mapping		19	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-Radiation Hybrid		19	J:59124 Kasik J, et al., Identification, chromosomal mapping, and partial characterization of mouse Ins16: a new member of the insulin family. Endocrinology. 2000 Jan;141(1):458-61
TEXT-Radiation Hybrid		19	J:63778 Simon-Chazottes D, et al., Genomic organization, chromosomal assignment, and expression analysis of the mouse suppressor of fused gene (Sufu) coding a Gli protein partner. Mamm Genome. 2000 Aug;11(8):614-21
TEXT-Radiation Hybrid		19	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;