A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Issue 1 (December 2017)
- Record Type:
- Journal Article
- Title:
- A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction. Issue 1 (December 2017)
- Main Title:
- A large scale hearing loss screen reveals an extensive unexplored genetic landscape for auditory dysfunction
- Authors:
- Bowl, Michael
Simon, Michelle
Ingham, Neil
Greenaway, Simon
Santos, Luis
Cater, Heather
Taylor, Sarah
Mason, Jeremy
Kurbatova, Natalja
Pearson, Selina
Bower, Lynette
Clary, Dave
Meziane, Hamid
Reilly, Patrick
Minowa, Osamu
Kelsey, Lois
Tocchini-Valentini, Glauco
Gao, Xiang
Bradley, Allan
Skarnes, William
Moore, Mark
Beaudet, Arthur
Justice, Monica
Seavitt, John
Dickinson, Mary
Wurst, Wolfgang
Angelis, Martin
Herault, Yann
Wakana, Shigeharu
Nutter, Lauryl
Flenniken, Ann
McKerlie, Colin
Murray, Stephen
Svenson, Karen
Braun, Robert
West, David
Lloyd, K.
Adams, David
White, Jacqui
Karp, Natasha
Flicek, Paul
Smedley, Damian
Meehan, Terrence
Parkinson, Helen
Teboul, Lydia
Wells, Sara
Steel, Karen
Mallon, Ann-Marie
Brown, Steve
… (more) - Abstract:
- Abstract The developmental and physiological complexity of the auditory system is likely reflected in the underlying set of genes involved in auditory function. In humans, over 150 non-syndromic loci have been identified, and there are more than 400 human genetic syndromes with a hearing loss component. Over 100 non-syndromic hearing loss genes have been identified in mouse and human, but we remain ignorant of the full extent of the genetic landscape involved in auditory dysfunction. As part of the International Mouse Phenotyping Consortium, we undertook a hearing loss screen in a cohort of 3006 mouse knockout strains. In total, we identify 67 candidate hearing loss genes. We detect known hearing loss genes, but the vast majority, 52, of the candidate genes were novel. Our analysis reveals a large and unexplored genetic landscape involved with auditory function. The full extent of the genetic basis for hearing impairment is unknown. Here, as part of the International Mouse Phenotyping Consortium, the authors perform a hearing loss screen in 3006 mouse knockout strains and identify 52 new candidate genes for genetic hearing loss.
- Is Part Of:
- Nature communications. Volume 8:Issue 1(2017)
- Journal:
- Nature communications
- Issue:
- Volume 8:Issue 1(2017)
- Issue Display:
- Volume 8, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 8
- Issue:
- 1
- Issue Sort Value:
- 2017-0008-0001-0000
- Page Start:
- 1
- Page End:
- 11
- Publication Date:
- 2017-12
- Subjects:
- Biology -- Periodicals
Physical sciences -- Periodicals
505 - Journal URLs:
- http://www.nature.com/ncomms/index.html ↗
http://www.nature.com/ ↗ - DOI:
- 10.1038/s41467-017-00595-4 ↗
- Languages:
- English
- ISSNs:
- 2041-1723
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6046.280270
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10806.xml