Literature DB >> 21179397

Fine Mapping of a Deafness Mutation hml on Mouse Chromosome 10.

Qing Yin Zheng1, Belinda S Harris, Patricia F Ward-Bailey, Heping Yu, Roderick T Bronson, Muriel T Davisson, Kenneth R Johnson.   

Abstract

OBJECTIVE: to map a mouse deafness gene, identify the underlying mutation and develop a mouse model for human deafness.
METHODS: genetic linkage cross and genome scan were used to map a novel mutation named hypoplasia of the membranous labyrinth (hml), which causes hearing loss in mutant mice.
RESULTS: 1. hml was mapped on mouse Chr 10 (~43 cM from the centromere) suggests that the homologous human gene is on 12q22-q24, which was defined on the basis of known mouse-human homologies (OMIM, 2004). 2. This study has generated 25 polymorphic microsatellite markers, placed 3 known human genes in the correct order in a high-resolution mouse map and narrowed the hml candidate gene region to a 500kb area.

Entities:  

Year:  2004        PMID: 21179397      PMCID: PMC3004367     

Source DB:  PubMed          Journal:  Acad J Xian Jiaotong Univ        ISSN: 1671-8267


  10 in total

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7.  The neurological mouse mutations jittery and hesitant are allelic and map to the region of mouse chromosome 10 homologous to 19p13.3.

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Authors:  K R Johnson; S A Cook; Q Y Zheng
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9.  Fine genetic and comparative mapping of the deafness mutation Ames waltzer on mouse chromosome 10.

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10.  Molecular characterization of a 12q22-q24 deletion associated with congenital deafness: confirmation and refinement of the DFNA25 locus.

Authors:  Erwin Petek; Christian Windpassinger; Monika Mach; Ludwig Rauter; Stephen W Scherer; Klaus Wagner; Peter M Kroisel
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  10 in total
  1 in total

Review 1.  Inner ear proteomics of mouse models for deafness, a discovery strategy.

Authors:  Qing Yin Zheng; Christine R Rozanas; Isolde Thalmann; Mark R Chance; Kumar N Alagramam
Journal:  Brain Res       Date:  2006-04-05       Impact factor: 3.252

  1 in total

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