Skip to search formSkip to main contentSkip to account menu

MYO15A gene

Known as: MYO15A, Myosin XVA Gene, MYO15 
This gene plays a role in the structure of stereocilia.
National Institutes of Health

Related topics

Related topics

6 relations
Cell MovementCytokinesisHearingMYO15A protein, human

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2019
2019
The prevalence of deafness-associated mutations in neonates: A meta-analysis of clinical trials.
2019
2019
Novel mutations in MYTH4-FERM domains of myosin 15 are associated with autosomal recessive nonsyndromic hearing loss.
Review
2017
Review
2017
Genetics Of Human Hereditary Hearing Impairment.
Hereditary hearing impairment is heterogeneous type of disorder which can be caused due to environmental as well as genetical… 
2015
2015
Identification of a Novel MYO15A Mutation in a Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
Autosomal recessive nonsyndromic hearing loss (ARNSHL) is a genetically heterogeneous sensorineural disorder, generally… 
2013
2013
A phylomedicine approach to understanding the evolution of auditory sensory perception and disease in mammals
Hereditary deafness affects 0.1% of individuals globally and is considered as one of the most debilitating diseases of man… 
2012
2012
Prioritized sequencing of the second exon of MYO15A reveals a new mutation segregating in a Pakistani family with moderate to severe hearing loss.
2009
2009
Screening of the DFNB3 locus: identification of three novel mutations of MYO15A associated with hearing loss and further suggestion for two distinctive genes on this locus.
Recessive mutations of MYO15A are associated with nonsyndromic hearing loss (HL) in humans (DFNB3) and in the shaker-2 mouse… 
2006
2006
Transgene correction maintains normal cochlear structure and function in 6-month-old Myo15a mutant mice
2004
2004
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 MYO15A gene… 
2003
2003
Myo15 function is distinct from Myo6, Myo7a and pirouette genes in development of cochlear stereocilia.
The unconventional myosin genes Myo15, Myo6 and Myo7a are essential for hearing in both humans and mice. Despite the expression… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)