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Symbol
Name
ID
Chromosome
D10Mit29
DNA segment, Chr 10, Massachusetts Institute of Technology 29
MGI:88812
10
10 mapping experiments
Experiment Type Details Chromosome Reference
CROSS Cross Type: Intercross
10 J:69655 Bryda EC, et al., High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and waltzer (cdh23(v)). Genomics. 2001 May 1;73(3):338-42
CROSS Cross Type: Backcross
10 J:38058 Bryda EC, et al., A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer. Mamm Genome. 1997 Jan;8(1):1-4
CROSS Cross Type: Backcross
10 J:38058 Bryda EC, et al., A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer. Mamm Genome. 1997 Jan;8(1):1-4
CROSS Cross Type: Intercross
10 J:142852 Chang B, et al., Age-related retinal degeneration (arrd2) in a novel mouse model due to a nonsense mutation in the Mdm1 gene. Hum Mol Genet. 2008 Dec 15;17(24):3929-41
CROSS Cross Type: Backcross
Mapping Panel: EUCIB (both)
10 J:56632 Smith DP, et al., The mouse Peutz-Jeghers syndrome gene Lkb1 encodes a nuclear protein kinase. Hum Mol Genet. 1999 Aug;8(8):1479-85
TEXT-Genetic Cross 10 J:38058 Bryda EC, et al., A high-resolution genetic map around waltzer on mouse chromosome 10 and identification of a new allele of waltzer. Mamm Genome. 1997 Jan;8(1):1-4
TEXT-Genetic Cross 10 J:69985 Wilson SM, et al., Mutations in Cdh23 Cause Nonsyndromic Hearing Loss in waltzer Mice. Genomics. 2001 Jun 1;74(2):228-33
TEXT-Physical Mapping 10 J:106743 Mouse Genome Informatics and NCBI UniSTS, UniSTS load for MIT markers. Database Download. 2006;
TEXT-Physical Mapping 10 J:69985 Wilson SM, et al., Mutations in Cdh23 Cause Nonsyndromic Hearing Loss in waltzer Mice. Genomics. 2001 Jun 1;74(2):228-33
TEXT-Radiation Hybrid 10 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
04/30/2024
MGI 6.23
The Jackson Laboratory