Source: CLINGEN

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
CUI: C1852282
Disease: DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder) 		0.300 Biomarker CLINGEN Myo1c mutations associated with hearing loss cause defects in the interaction with nucleotide and actin. 20640478

2011
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
CUI: C1852282
Disease: DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder) 		0.300 Biomarker CLINGEN Are MYO1C and MYO1F associated with hearing loss? 19027848

2009
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C
CUI: C1852282
Disease: DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder)
DEAFNESS, AUTOSOMAL DOMINANT 1 (disorder) 		0.300 Biomarker CLINGEN Myosin-I isozymes in neonatal rodent auditory and vestibular epithelia. 12486594

2002