Mapping Data Summary

• Symbol: D13Mit29
• Name: DNA segment, Chr 13, Massachusetts Institute of Technology 29
• ID: MGI:89756
• Chromosome: 13

8 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	13	J:22444 O'Brien EP, et al., Molecular markers near two mouse chromosome 13 genes, muted and pearl, which cause platelet storage pool deficiency (SPD). Mamm Genome. 1995 Jan;6(1):19-24
CROSS	Cross Type: Backcross	13	J:42685 Sagai T, et al., rim2 (recombination induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak Syndrome (HPS): genetic and physical mapping. Mamm Genome. 1997;9(1):2-7
CROSS	Cross Type: Backcross	13	J:42685 Sagai T, et al., rim2 (recombination induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak Syndrome (HPS): genetic and physical mapping. Mamm Genome. 1997;9(1):2-7
TEXT		13	J:33579 Seymour AB, et al., An integrated genetic map of the pearl locus of mouse chromosome 13. Genome Res. 1996 Jun;6(6):538-44
TEXT-Genetic Cross		13	J:52879 Feng L, et al., The beta3A subunit gene (Ap3b1) of the AP-3 adaptor complex is altered in the mouse hypopigmentation mutant pearl, a model for Hermansky-Pudlak syndrome and night blindness. Hum Mol Genet. 1999 Feb;8(2):323-30
TEXT-Genetic Cross		13	J:33579 Seymour AB, et al., An integrated genetic map of the pearl locus of mouse chromosome 13. Genome Res. 1996 Jun;6(6):538-44
TEXT-Physical Mapping		13	J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-Physical Mapping		13	J:42685 Sagai T, et al., rim2 (recombination induced mutation 2) is a new allele of pearl and a mouse model of human Hermansky-Pudlak Syndrome (HPS): genetic and physical mapping. Mamm Genome. 1997;9(1):2-7