Mapping Data Summary

• Symbol: Cdh23
• Name: cadherin related 23 (otocadherin)
• ID: MGI:1890219
• Chromosome: 10

44 mapping experiments

Experiment Type	Details	Chromosome	Reference
CROSS	Cross Type: Backcross	10	J:13695 Beechey CV, et al., Linkage of Sl^con and gr. Mouse News Lett. 1976;55:15
CROSS	Cross Type: Intercross	10	J:11987 Bloom JL, et al., "Grizzled", a mutant in linkage group X of the mouse. Genet Res. 1966;7(2):159-167
CROSS	Cross Type: Backcross	10	J:11987 Bloom JL, et al., "Grizzled", a mutant in linkage group X of the mouse. Genet Res. 1966;7(2):159-167
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: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: Backcross	10	J:6308 Crocker M, et al., The genetics of Sleek: a possible regulatory mutation of the tabby-crinkled-downless syndrome. Genet Res. 1979 Dec;34(3):231-8
CROSS	Cross Type: Backcross	10	J:17606 Everett CA, et al., Mapping of six dominant cataract genes in the mouse. Genomics. 1994 Apr;20(3):429-34
CROSS	Cross Type: Backcross	10	J:44966 Johnson KR, et al., A major gene affecting age-related hearing loss in C57BL/6J mice. Hear Res. 1997 Dec;114(1-2):83-92
CROSS	Cross Type: Backcross	10	J:44966 Johnson KR, et al., A major gene affecting age-related hearing loss in C57BL/6J mice. Hear Res. 1997 Dec;114(1-2):83-92
CROSS	Cross Type: Backcross	10	J:34741 Lyon MF, et al., Linkage data - suggested order v-gr-T199 break. Mouse News Lett. 1972;46:29
CROSS	Cross Type: Backcross	10	J:6702 Lyon MF, et al., Lens opacity: a new gene for congenital cataract on chromosome 10 of the mouse. Genet Res. 1981 Dec;38(3):337-41
CROSS	Cross Type: Backcross	10	J:6702 Lyon MF, et al., Lens opacity: a new gene for congenital cataract on chromosome 10 of the mouse. Genet Res. 1981 Dec;38(3):337-41
CROSS	Cross Type: Backcross	10	J:6702 Lyon MF, et al., Lens opacity: a new gene for congenital cataract on chromosome 10 of the mouse. Genet Res. 1981 Dec;38(3):337-41
CROSS	Cross Type: Intercross	10	J:38429 Noben-Trauth K, et al., mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw). Genomics. 1997 Sep 15;44(3):266-72
CROSS	Cross Type: Intercross	10	J:300 Snell GD, Linkage of jittery and waltzing in the mouse. J Hered. 1945;36(9):279-80
CROSS	Cross Type: Backcross	10	J:300 Snell GD, Linkage of jittery and waltzing in the mouse. J Hered. 1945;36(9):279-80
CROSS	Cross Type: Backcross	10	J:6020 Womack JE, et al., An acid phosphatase locus expressed in mouse kidney (Apk) and its genetic location on chromosome 10. Biochem Genet. 1978 Apr;16(3-4):239-45
TEXT		10	J:44966 Johnson KR, et al., A major gene affecting age-related hearing loss in C57BL/6J mice. Hear Res. 1997 Dec;114(1-2):83-92
TEXT		10	J:44966 Johnson KR, et al., A major gene affecting age-related hearing loss in C57BL/6J mice. Hear Res. 1997 Dec;114(1-2):83-92
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		10	J:139222 Zheng QY, et al., A locus on distal chromosome 10 (ahl4) affecting age-related hearing loss in A/J mice. Neurobiol Aging. 2009 Oct;30(10):1693-705
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:13681 Green MC, et al., Chromosome 10. Mouse News Lett. 1975;53:34
TEXT-Genetic Cross		10	J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003;
TEXT-Genetic Cross		10	J:82238 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2003;
TEXT-Genetic Cross		10	J:87349 JAX Neuroscience Mutagenesis Facility, Heritable mouse mutants from JAX NMF ENU Mutagenesis Program. MGI Direct Data Submission. 2004-7;
TEXT-Genetic Cross		10	J:66228 Johnson KR, et al., A major gene affecting age-related hearing loss is common to at least ten inbred strains of mice. Genomics. 2000 Dec 1;70(2):171-80
TEXT-Genetic Cross		10	J:97534 Johnson KR, et al., The Mass1(frings) mutation underlies early onset hearing impairment in BUB/BnJ mice, a model for the auditory pathology of Usher syndrome IIC. Genomics. 2005 May;85(5):582-90
TEXT-Genetic Cross		10	J:34741 Lyon MF, et al., Linkage data - suggested order v-gr-T199 break. Mouse News Lett. 1972;46:29
TEXT-Genetic Cross		10	J:38429 Noben-Trauth K, et al., mdfw: a deafness susceptibility locus that interacts with deaf waddler (dfw). Genomics. 1997 Sep 15;44(3):266-72
TEXT-Genetic Cross		10	J:119820 Schwander M, et al., A forward genetics screen in mice identifies recessive deafness traits and reveals that pejvakin is essential for outer hair cell function. J Neurosci. 2007 Feb 28;27(9):2163-75
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: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
TEXT-Physical Mapping		10	J:66698 Di Palma F, et al., Mutations in cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for usher syndrome type 1D. Nat Genet. 2001 Jan;27(1):103-7
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:80000 The FANTOM Consortium and The RIKEN Genome Exploration Research Group Phase I & II Team, Analysis of the mouse transcriptome based on functional annotation of 60,770 full-length cDNAs. Nature. 2002;420:563-573
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-QTL		10	J:105889 Drayton M, et al., Mapping quantitative trait loci for hearing loss in Black Swiss mice. Hear Res. 2006 Feb;212(1-2):128-39
TEXT-QTL		10	J:111682 Mashimo T, et al., Two quantitative trait loci affecting progressive hearing loss in 101/H mice. Mamm Genome. 2006 Aug;17(8):841-50
TEXT-QTL		10	J:128536 Watanabe A, et al., Fabp7 maps to a quantitative trait locus for a schizophrenia endophenotype. PLoS Biol. 2007 Nov;5(11):e297
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