Mapping Data Summary

• Symbol: D19Mit17
• Name: DNA segment, Chr 19, Massachusetts Institute of Technology 17
• ID: MGI:91225
• Chromosome: 19

26 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 Mapping Panel: Kozak Skive (NFS/N)	19	J:56825 Kozak CA, et al., Identification and genetic mapping of differentially expressed genes in mice differing at the If1 interferon regulatory locus. Mamm Genome. 1999 Sep;10(9):853-7
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:42393 Lammert F, et al., The gene encoding the multispecific organic anion transporter of the hepatocyte canalicular membraine (Cmoat) maps to mouse Chromosome 19. Mamm Genome. 1998 Jan;9(1):87-88
CROSS	Cross Type: Backcross Mapping Panel: Kozak FvC58 + FvSpr	19	J:54005 Lee CG, et al., Genetic mapping of eight SH3 domain genes on seven mouse chromosomes. Mamm Genome. 1999 Apr;10(4):402-4
CROSS	Cross Type: Backcross Mapping Panel: Kozak Skive (C58/J or NFS/N)	19	J:54005 Lee CG, et al., Genetic mapping of eight SH3 domain genes on seven mouse chromosomes. Mamm Genome. 1999 Apr;10(4):402-4
CROSS	Cross Type: Backcross Mapping Panel: Kozak FvC58 + FvSpr	19	J:42072 Luo G, et al., Mapping of the gene (NRAP) encoding N-RAP in the mouse and human genomes. Genomics. 1997 Oct 1;45(1):229-32
CROSS	Cross Type: Backcross Mapping Panel: Kozak Skive (C58/J or NFS/N)	19	J:42072 Luo G, et al., Mapping of the gene (NRAP) encoding N-RAP in the mouse and human genomes. Genomics. 1997 Oct 1;45(1):229-32
CROSS	Cross Type: Backcross Mapping Panel: Kozak FvC58 + FvSpr	19	J:62456 Lyu MS, et al., Genetic mapping of six mouse peroxiredoxin genes and fourteen peroxiredoxin related sequences. Mamm Genome. 1999 Oct;10(10):1017-9
CROSS	Cross Type: Backcross Mapping Panel: Kozak Skive	19	J:62456 Lyu MS, et al., Genetic mapping of six mouse peroxiredoxin genes and fourteen peroxiredoxin related sequences. Mamm Genome. 1999 Oct;10(10):1017-9
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
CROSS	Cross Type: Backcross Mapping Panel: JAX (BSS)	19	J:59226 Suriyapperuma SP, et al., The mouse adducin gene family: alternative splicing and chromosomal localization. Mamm Genome. 2000 Jan;11(1):16-23
RI	RI/RC Set: OcB	19	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: CcS	19	J:31555 Stassen AP, et al., Genetic composition of the recombinant congenic strains. Mamm Genome. 1996 Jan;7(1):55-8
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: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-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
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;