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Publication : A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate.

First Author  Paige AJ Year  2000
Journal  Mamm Genome Volume  11
Issue  1 Pages  51-7
PubMed ID  10602993 Mgi Jnum  J:59252
Mgi Id  MGI:1351246 Doi  10.1007/s003350010010
Citation  Paige AJ, et al. (2000) A deletion on chromosome 4 cosegregates with the whirler deafness mutation: exclusion of Orm1 as a candidate. Mamm Genome 11(1):51-7
abstractText  Whirler (wi) mice display profound deafness and a head-tossing and circling phenotype, showing an autosomal recessive mode of inheritance. The wi mutation has been shown to map close to the Orm gene cluster on mouse Chromosome (Chr) 4. We have, therefore, investigated the Orm loci as candidates for the whirler gene. Detailed mapping and analysis of the Orm gene cluster in both normal and whirler mice indicates the presence of a <48-kb deletion in whirler mice that disrupts the Orm1 locus. The Orm1 locus is also deleted in the CE/J mouse strain, and we discuss the candidature of Orm1 for the whirler gene.
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