Gene: MYO1C ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C 		0.300 Biomarker disease 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 		0.300 Biomarker disease CLINGEN Are MYO1C and MYO1F associated with hearing loss? 19027848 2009
Entrez Id: 4641
Gene Symbol: MYO1C
MYO1C 		0.300 Biomarker disease CLINGEN Myosin-I isozymes in neonatal rodent auditory and vestibular epithelia. 12486594 2002