Literature DB >> 11350126

High-resolution genetic and physical mapping of modifier-of-deafwaddler (mdfw) and Waltzer (Cdh23v).

E C Bryda1, H J Kim, M E Legare, W N Frankel, K Noben-Trauth.   

Abstract

Modifier-of-deafwaddler (mdfw) and waltzer (Cdh23v) are loci on mouse chromosome 10 encoding factors that are essential for the function of auditory hair cells. The BALB/cByJ-specific mdfw allele encodes a necessary and sufficient modifier that induces progressive early onset hearing loss in CBy-dfw2J heterozygotes. Recessive mutations in the waltzer locus result in circling behavior and congenital deafness. In this report we present a high-resolution integrated genetic and physical map of mdfw and Cdh23(v). Our genetic analyses localize mdfw between markers D10Mit60 and 148M13T7 within a 1.01-cM region. The Cdh23v critical interval is fully contained within the mdfw region and localizes between markers 146O23T7 and 148M13T7 within a 0.35-cM interval that is represented in an approximately 500-kb BAC contig. Our data suggest that mdfw and Cdh23v are allelic. Copyright 2001 Academic Press.

Entities:  

Mesh:

Year:  2001        PMID: 11350126     DOI: 10.1006/geno.2001.6538

Source DB:  PubMed          Journal:  Genomics        ISSN: 0888-7543            Impact factor:   5.736


  6 in total

Review 1.  Strain background effects and genetic modifiers of hearing in mice.

Authors:  Kenneth R Johnson; Qing Yin Zheng; Konrad Noben-Trauth
Journal:  Brain Res       Date:  2006-03-31       Impact factor: 3.252

2.  Phenotypic variability of patients homozygous for the GJB2 mutation 35delG cannot be explained by the influence of one major modifier gene.

Authors:  Nele Hilgert; Matthew J Huentelman; Ashley Q Thorburn; Erik Fransen; Nele Dieltjens; Malgorzata Mueller-Malesinska; Agnieszka Pollak; Agata Skorka; Jaroslaw Waligora; Rafal Ploski; Pierangela Castorina; Paola Primignani; Umberto Ambrosetti; Alessandra Murgia; Eva Orzan; Arti Pandya; Kathleen Arnos; Virginia Norris; Pavel Seeman; Petr Janousek; Delphine Feldmann; Sandrine Marlin; Françoise Denoyelle; Carla J Nishimura; Andreas Janecke; Doris Nekahm-Heis; Alessandro Martini; Elena Mennucci; Timea Tóth; Istvan Sziklai; Ignacio Del Castillo; Felipe Moreno; Michael B Petersen; Vasiliki Iliadou; Mustafa Tekin; Armagan Incesulu; Ewa Nowakowska; Jerzy Bal; Paul Van de Heyning; Anne-Françoise Roux; Catherine Blanchet; Cyril Goizet; Guenaëlle Lancelot; Graça Fialho; Helena Caria; Xue Zhong Liu; Ouyang Xiaomei; Paul Govaerts; Karen Grønskov; Karianne Hostmark; Klemens Frei; Ingeborg Dhooge; Stephen Vlaeminck; Erdmute Kunstmann; Lut Van Laer; Richard J H Smith; Guy Van Camp
Journal:  Eur J Hum Genet       Date:  2008-11-05       Impact factor: 4.246

Review 3.  Genetics of hearing and deafness.

Authors:  Simon Angeli; Xi Lin; Xue Zhong Liu
Journal:  Anat Rec (Hoboken)       Date:  2012-10-08       Impact factor: 2.064

4.  Progressive hearing loss and increased susceptibility to noise-induced hearing loss in mice carrying a Cdh23 but not a Myo7a mutation.

Authors:  Ralph H Holme; Karen P Steel
Journal:  J Assoc Res Otolaryngol       Date:  2003-12-18

5.  Modifiers of hearing impairment in humans and mice.

Authors:  Denise Yan; Xue-Zhong Liu
Journal:  Curr Genomics       Date:  2010-06       Impact factor: 2.236

6.  The sound of silence: mouse models for hearing loss.

Authors:  Sumantra Chatterjee; Thomas Lufkin
Journal:  Genet Res Int       Date:  2011-10-09
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.