Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.310 Biomarker CLINGEN Class III myosins shape the auditory hair bundles by limiting microvilli and stereocilia growth. 26754646

2016
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.310 Biomarker 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
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.310 Biomarker CLINGEN Diagnostic application of targeted resequencing for familial nonsyndromic hearing loss. 23990876

2013
Entrez Id: 53904
Gene Symbol: MYO3A
MYO3A
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.310 Biomarker 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
CUI: C3711374
Disease: Nonsyndromic Deafness
Nonsyndromic Deafness 		0.310 Biomarker CLINGEN From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30. 12032315

2002