Mapping Data Summary

• Symbol: D10Mit48
• Name: DNA segment, Chr 10, Massachusetts Institute of Technology 48
• ID: MGI:88831
• Chromosome: 10

14 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: Other	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: 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
TEXT		10	J:69028 Wada T, et al., A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata. Biochem Biophys Res Commun. 2001 Apr 27;283(1):113-7
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-Genetic Cross		10	J:57150 Yonezawa S, et al., Chromosomal localization of a gene responsible for vestibulocochlear defects of BUS/Idr mice: identification as an allele of waltzer. Hear Res. 1999 Aug;134(1-2):116-22
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:86905 Noben-Trauth K, et al., Association of cadherin 23 with polygenic inheritance and genetic modification of sensorineural hearing loss. Nat Genet. 2003 Sep;35(1):21-3
TEXT-Physical Mapping		10	J:69028 Wada T, et al., A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata. Biochem Biophys Res Commun. 2001 Apr 27;283(1):113-7
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: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