Gene: MYO3A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A 		0.310 AlteredExpression disease BEFREE Myo3a is expressed in cochlear hair cells and retinal cells and is responsible for human recessive hereditary nonsyndromic deafness (DFNB30). 30123247 2018
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A 		0.310 Biomarker disease CLINGEN Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth. 26754646 2016
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A 		0.310 Biomarker disease CLINGEN Identification of a novel homozygous mutation in MYO3A in a Chinese family with DFNB30 non-syndromic hearing impairment. 27063751 2016
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A 		0.310 Biomarker disease CLINGEN Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss. 23990876 2013
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A 		0.310 Biomarker disease CLINGEN A mouse model for human hearing loss DFNB30 due to loss of function of myosin IIIA. 21165622 2011
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A 		0.310 Biomarker disease CLINGEN From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30. 12032315 2002