Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
Sensorineural hearing loss, bilateral
0.300 Biomarker CLINGEN Three heterozygous missense mutations in the motor domain of myosin 1c (Myo1c), which mediates adaptation in the inner ear, are associated with bilateral sensorineural hearing loss in humans. 20640478

2011

Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
Sensorineural hearing loss, bilateral
0.300 Biomarker CLINGEN To better understand the role of this gene family we performed a mutational screening on two candidate genes, MYO1C and MYO1F, analyzing hundreds of patients, affected by bilateral sensorineural hearing loss and coming from different European countries. 19027848

2009

Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
Sensorineural hearing loss, bilateral
0.300 Biomarker CLINGEN Myosin-I isozymes in neonatal rodent auditory and vestibular epithelia. 12486594

2002