Cloning and chromosomal localization of MYO15A to chromosome 5 of the dog (Canis familiaris)

Mutations in the myosin XVA gene (MYO15A) cause congenital non-syndromic deafness in humans and mice. Therefore, the M YO15A gene represents a candidate gene for hereditary hearing loss in dogs. Using a human cDNA to screen a dog BAC library, we isolated a canine BAC clone. Sequencing of the BAC end...

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Veröffentlicht in:Chromosome research 2002-01, Vol.10 (5), p.407-410
Hauptverfasser: Rak, Simone G, Drögemüller, Cord, Kuiper, Heidi, Leeb, Tosso, Quignon, Pascale, André, Catherine, Distl, Ottmar
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container_end_page 410
container_issue 5
container_start_page 407
container_title Chromosome research
container_volume 10
creator Rak, Simone G
Drögemüller, Cord
Kuiper, Heidi
Leeb, Tosso
Quignon, Pascale
André, Catherine
Distl, Ottmar
description Mutations in the myosin XVA gene (MYO15A) cause congenital non-syndromic deafness in humans and mice. Therefore, the M YO15A gene represents a candidate gene for hereditary hearing loss in dogs. Using a human cDNA to screen a dog BAC library, we isolated a canine BAC clone. Sequencing of the BAC ends confirmed homology to the human gene. To facilitate future linkage studies, we report the physical mapping of the canine MYO15A gene to CFA5q23-q24 by FISH and RH mapping.
doi_str_mv 10.1023/A:1016805803686
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subjects Animals
Bacterial artificial chromosomes
Canis familiaris
Chromosome 5
Chromosome Banding
Cloning
Cloning, Molecular
Deafness
Dogs
Gene mapping
Genes
Genetics
Genome
Hearing loss
Hearing Loss, Sensorineural - genetics
Homology
Humans
In Situ Hybridization, Fluorescence
Localization
Molecular Sequence Data
Mutation
Myosin
Myosins - genetics
Physical Chromosome Mapping
Physical mapping
Radiation Hybrid Mapping
title Cloning and chromosomal localization of MYO15A to chromosome 5 of the dog (Canis familiaris)
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