Mapping Data Summary

• Symbol: D13Mit28
• Name: DNA segment, Chr 13, Massachusetts Institute of Technology 28
• ID: MGI:89755
• Chromosome: 13

12 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Intercross	13	J:54856 Benavides F, et al., Nackt (nkt), a new hair loss mutation of the mouse with associated CD4 deficiency. Immunogenetics. 1999 May;49(5):413-9
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 Mapping Panel: EUCIB (BSB)	13	J:32825 Poirier C, et al., The gene encoding the thrombin receptor (Cf2r) maps to mouse Chromosome 13. Mamm Genome. 1996 Apr;7(4):322
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:29850 Vinik BS, et al., Mapping of the MEK kinase gene (Mekk) to mouse chromosome 13 and human chromosome 5. Mamm Genome. 1995 Nov;6(11):782-3
CROSS	Cross Type: Backcross Mapping Panel: EUCIB (BSB)	13	J:38576 Viollet L, et al., cDNA isolation, expression, and chromosomal localization of the mouse survival motor neuron gene (Smn). Genomics. 1997 Feb 15;40(1):185-8
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
TEXT-Radiation Hybrid		13	J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;