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Symbol
Name
ID
Chromosome
D13Mit87
DNA segment, Chr 13, Massachusetts Institute of Technology 87
MGI:89816
13
8 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Intercross
13 J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
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: Unspecified
13 J:38300 Perou CM, et al., Comparative mapping in the beige-satin region of mouse chromosome 13. Genomics. 1997 Jan 15;39(2):136-46
TEXT-Genetic Cross 13 J:54407 Hong HK, et al., Pleiotropic skeletal and ocular phenotypes of the mouse mutation congenital hydrocephalus (ch/Mf1) arise from a winged helix/forkhead transcriptionfactor gene. Hum Mol Genet. 1999 Apr;8(4):625-37
TEXT-Genetic Cross 13 J:75830 Zhang Q, et al., The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking. Hum Mol Genet. 2002 Mar 15;11(6):697-706
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:75830 Zhang Q, et al., The gene for the muted (mu) mouse, a model for Hermansky-Pudlak syndrome, defines a novel protein which regulates vesicle trafficking. Hum Mol Genet. 2002 Mar 15;11(6):697-706
TEXT-Radiation Hybrid 13 J:68900 The Jackson Laboratory Mouse Radiation Hybrid Database, Mouse T31 Radiation Hybrid Data Load. Database Release. 2004;

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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory