Mapping Data Summary

• Symbol: D19Umi1
• Name: DNA segment, Chr 19, University of Michigan 1
• ID: MGI:91342
• Chromosome: 19

12 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	19	J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9
CROSS	Cross Type: Backcross	19	J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9
CROSS	Cross Type: Backcross	19	J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9
CROSS	Cross Type: Backcross	19	J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20
CROSS	Cross Type: Backcross	19	J:18648 O'Brien EP, et al., Molecular map of chromosome 19 including three genes affecting bleeding time: ep, ru, and bm. Mamm Genome. 1994 Jun;5(6):356-60
CROSS	Cross Type: Intercross	19	J:68175 Rieger DK, et al., A double-deletion mutation in the pitx3 gene causes arrested lens development in aphakia mice. Genomics. 2001 Feb 15;72(1):61-72
TEXT		19	J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20
TEXT		19	J:57316 Sidow A, et al., A novel member of the F-box/WD40 gene family, encoding dactylin, is disrupted in the mouse dactylaplasia mutant. Nat Genet. 1999 Sep;23(1):104-7
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-Genetic Cross		19	J:56826 Herron BJ, et al., Scraggly, a new hair loss mutation on mouse chromosome 19. Mamm Genome. 1999 Sep;10(9):864-9
TEXT-Genetic Cross		19	J:20807 Keller SA, et al., Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus. Genomics. 1994 Sep 15;23(2):309-20
TEXT-Physical Mapping		19	J:68175 Rieger DK, et al., A double-deletion mutation in the pitx3 gene causes arrested lens development in aphakia mice. Genomics. 2001 Feb 15;72(1):61-72